Jump to content
RemedySpot.com

Re: Re:The future of our children

Rate this topic


Guest guest

Recommended Posts

Guest guest



As far as church goes. I am with Robin.. I have never felt so unaccepted as when I attempted church with my kids. With my son's age group there was a little old lady who gave out candy to all the "good " kids after Sunday School . Of course, she always left my kids out since they were not "good" (meaning quiet). When I tried again with my granddaughter, it went ok until the day they introduced loud music to the program, and she wouldn't participate and, again, the little old lady that was the class "shepherd" screamed across the whole Sunday School gathering that "That girl needs therapy!" and later explained that she was only trying to let us know that she is in deep need of help. She harrassed several other kids, too, but my husband would no longer attend church, nor my daughter and I have quit trying too. I talk to God at home.

( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06 teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

Link to comment
Share on other sites

Guest guest

I agree with where schools' emphasis' are.

But,,,,,,,how do you teach to socially fit? Yep, I know that there are groups and classes, but for us, they weren't worth a dime. I remember Ian had Social Skills Class 1 time per week for 20 mins. This was also when the school had thier Assembly's. Ugh.

I may get beat up for this, but I think our kids can learn HOW to react socially but it will NEVER flow naturally. My son addresses everyone. Can say, "Fine thanks, how are you?", but it isn't "natural, if that makes sense.

I think the world would be better off to "get" those darned kids who haven't been taught to be nice. To get the kids that would rather get a laugh than to include others. Shame, also, on the teachers who look the other way or won't / can't jump in and make them be nice.

It's so simple, isn't it? hee hee. I wish.

Attack and enjoy every minute of life.

Try everything.....protect everything.

Robin

From: Mimi <sue@...>Subject: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 12:21 PM

Ah ha! I think that you are so right. The social skill aspect is a large part of the equation. Someone on here used to sign their posts "Normal is just a cycle on a washing machine." I loved that quote. And therefore I say, "IQ is just a number." It is not a predictor of outcome, or success or failure in any case. In my limited observation, and I don't want to generalize, there are many kids with disabilities that are not part of the spectrum who are loved by everyone around them! They have the kind of social skills that make other kids take them under their wing, befriend them, want to protect them. Maybe not socialize with them...However, many of our kids do not have these personality traits. They say or do the wrong things, or have inappropriate reactions and poor social skills. In the long run, that, in my opinion only, is what is the biggest factor for success. So tell me why we put so much more emphasis on academic tutoring, help etc

and less on this when they are in school! We have it backwards.Sue in Tn> > > From: <teamjakob06@...>> Subject: Re: ( ) Re:The future of our children> > Date: Tuesday, July 20, 2010, 10:27 AM> > > Â > > > > > > > I

personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more

then one is another, of course the out come will be> different as well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}.  >  TeamJakob> Support children with > Aspergers,> With your support their is > no limit to Jakob's success!! > > > > > > > From: Comtois <suetoiscox (DOT) net>> > Sent: Tue, July 20, 2010 9:39:05 AM> Subject: ( ) Re:The future of our children> >  > > > I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children.  And I hope you're right.  I hope what you're doing with your son will head off the many problems that develop as these children get older.  We have three sons

with AS.  The oldest is 19.  The other two are 15 and 12.  The 15 yo is less affected, and will, I think, have a relatively normal future.  The 19 yo and the 12 yo are facing a different set of challenges.  > > > When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him.  There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental.  He also had a friend and we had just learned that his verbal IQ was/is about 200.  He taught himself to read grown-up novels shortly after his third birthday.  He was truly brilliant.  I was envisioning a future for him that might include being an author or a college professor.  You know, quirky, but brilliant. > > > When he was 7 1/2 the military transferred us to a different state, and we

elected to move into a district that had a fabulous program for gifted kids. Â The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).> > > At 8yo he was moved to a full-time gifted program. Â I was so proud of him and it just reinforced my hopes for his future. Â AS wasn't going to stand in the way of anything for my son. Â It wasn't going to be an excuse for a failure to achieve. Â Yeay! Â Unfortunately, a gifted program involves lots of transitions all the time. Â The typical gifted children thrived, but my son was totally overwhelmed. Â The day came when the principal told us that if we brought him back to school the next day, he would expel him. Â I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for

the next couple of years--all the while working on social skills and learning coping mechanisms. Â He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. Â The school> agreed, and, again, I was hopeful that things were back on track for a successful future.> > > Middle school was a mess. Â He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. Â The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Â Well, so much for that brilliant academic future. Â LD classes don't move as quickly as even general ed. classes

for obvious reasons.> > > High school rolled around, and my son got a wonderful case manager who took a personal interest in him. Â He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. Â But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. Â You see he has executive functioning deficits. Â Keeping himself as organized as a typical high school student is literally impossible for him. Â Where could he get more help with staying organized? Â The LD classes. Â He did, however, have some non-special ed. classes. Â Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Â Also, by now his lack of friends was really hurting him. Â He wrote an

entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. Â I got a> call to come to the school immediately. Â We talked with his case manager and I took our son home for a mental health day. Â We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. Â He was also in social skills therapy with a social worker, and we brought her in on the problem. Â The specialists couldn't really do much about the root of the problem though. Â The boy was lonely and you can't *make* other kids accept someone as a friend. Â We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal

interests and ignore each other. Â > > > Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. Â I was still thinking that a 4-year college was a natural choice for such a smart kid. Â The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. Â I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Â Our son's social worker told me that AS kids "crash and burn" in college. Â Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant

her the credentials she would need to become a teacher. Â She fell apart (including moving out and> becoming homeless for a while), and her mother was desperately trying to pick up the pieces.> > > We decided to let our son try the high school's technical school. Â Two years later, he has five professional certifications in the computer repair/website design area. Â He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Â Lack of social skills. Â For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Â Also, that executive functioning issue is rearing it's ugly head again. Â He can't really problem solve the way he would need to be able to in a professional capacity.> >

> Then there are the day to day issues. Â He can't remember to take his medicine by himself. Â Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Â Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. Â If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.> > > So here we are. Â He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). Â His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. Â I've had him evaluated by the Department of Rehabilitative

Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. Â I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. Â There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. Â I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of> overwhelmed and *he* certainly can't do it himself.> > > This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. Â The social and executive function deficits are *so* much more handicapping than you think they are when your child

is very young.  Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning.  Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.> > > As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future.  It truly is heartbreaking.  I know because we're living it.  My son is still a wonderful person.  He's sweet and innocent in a way that other people aren't.  He's cute.  He's brilliant.  And yet none of that is enough to keep him from having the sort of limited future I could  never have envisioned for him when he was 7yo.> > > I sincerely hope that your experience with AS follows a different pathway from ours.  It's entirely

possible that it will because every person with AS is different from every other person with AS.  I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.> > > Peace.> Sue> > > > > > > The future of our children> Posted by: "" teamjakob06   teamjakob06> Mon Jul 19, 2010 12:48 pm (PDT)> > > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child

in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and> our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. > > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised.

Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar! > > >

Link to comment
Share on other sites

Guest guest

Yep........sigh.

I was the one who used to have "Normal is just a cycle on a washing machine" as a signature.

I remember my mom always saying it. See,,,,my brother, had he been a student now, would have ADD/ADHD/AS for sure. But, it was in the days when a teacher could actually call a child "lazy". My folks were told that he had such a high IQ,,,,,they didn't understand why he was "so lazy".Anyway, don't know if she got that phrase from somewhere else or not, but as she was sitting wtih him at the dining room table till 10 at night, both of them crying and doing HIS homework, she's say things like the "normal" phrase.

That's where I got my thinking that "everyone's got something" from. I think all of us parents have some little phrases that stick with us.

*****After thinking about our conversations today, I really DO see a better "world" for kids with AS and spectrum issues some day. Things take time, sadly.

What we are going though now, or have gone though..........well, these are going to help the future kiddo's. Many of us will suffer, yep........go through bad things. Many of our kids won't get the services, let alone understanding and compassion that they deserve,,,,,,but we gotta keep on and know that in time, understanding DOES come.

Attack and enjoy every minute of life.

Try everything.....protect everything.

Robin

From: rushen janice <jrushen@...>Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 12:38 PM

Oh so true....IQ and class number are just that NUMBERS. Do they really mean anything in the real world? I have my doubts. What good is it to be #9 in your class if you can't handle transition ...or attend graduation.. ..or hold a job because you can't handle the noise or smell or don't know how to handle social situations.

"In the Midst of Difficulty lies Opportunity" Albert Einstein

Success is not measured by one's position but by the obstacles one has overcome to obtain that position

From: Mimi <suelowerydesign (DOT) com> Sent: Tue, July 20, 2010 1:21:36 PMSubject: ( ) Re:The future of our children

Ah ha! I think that you are so right. The social skill aspect is a large part of the equation. Someone on here used to sign their posts "Normal is just a cycle on a washing machine." I loved that quote. And therefore I say, "IQ is just a number." It is not a predictor of outcome, or success or failure in any case. In my limited observation, and I don't want to generalize, there are many kids with disabilities that are not part of the spectrum who are loved by everyone around them! They have the kind of social skills that make other kids take them under their wing, befriend them, want to protect them. Maybe not socialize with them...However, many of our kids do not have these personality traits. They say or do the wrong things, or have inappropriate reactions and poor social skills. In the long run, that, in my opinion only, is what is the biggest factor for success. So tell me why we put so much more emphasis on academic tutoring, help etc

and less on this when they are in school! We have it backwards.Sue in Tn> > > From: <teamjakob06@ ...>> Subject: Re: ( ) Re:The future of our children> > Date: Tuesday, July 20, 2010, 10:27 AM> > > Â > > > > > >

> I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing

and having more then one is another, of course the out come will be> different as well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}.  >  TeamJakob> Support children with > Aspergers,> With your support their is > no limit to Jakob's success!! > > > > > > > From: Comtois <suetoiscox (DOT) net>> > Sent: Tue, July 20, 2010 9:39:05 AM> Subject: ( ) Re:The future of our children> >  > > > I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children.  And I hope you're right.  I hope what you're doing with your son will head off the many problems that develop as these children get older.

 We have three sons with AS.  The oldest is 19.  The other two are 15 and 12.  The 15 yo is less affected, and will, I think, have a relatively normal future.  The 19 yo and the 12 yo are facing a different set of challenges.  > > > When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him.  There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental.  He also had a friend and we had just learned that his verbal IQ was/is about 200.  He taught himself to read grown-up novels shortly after his third birthday.  He was truly brilliant.  I was envisioning a future for him that might include being an author or a college professor.  You know, quirky, but brilliant. > > > When he was 7 1/2 the military transferred us to a

different state, and we elected to move into a district that had a fabulous program for gifted kids. Â The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).> > > At 8yo he was moved to a full-time gifted program. Â I was so proud of him and it just reinforced my hopes for his future. Â AS wasn't going to stand in the way of anything for my son. Â It wasn't going to be an excuse for a failure to achieve. Â Yeay! Â Unfortunately, a gifted program involves lots of transitions all the time. Â The typical gifted children thrived, but my son was totally overwhelmed. Â The day came when the principal told us that if we brought him back to school the next day, he would expel him. Â I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and

homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. Â He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. Â The school> agreed, and, again, I was hopeful that things were back on track for a successful future.> > > Middle school was a mess. Â He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. Â The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Â Well, so much for that brilliant academic future. Â LD classes don't move as quickly as even

general ed. classes for obvious reasons.> > > High school rolled around, and my son got a wonderful case manager who took a personal interest in him. Â He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. Â But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. Â You see he has executive functioning deficits. Â Keeping himself as organized as a typical high school student is literally impossible for him. Â Where could he get more help with staying organized? Â The LD classes. Â He did, however, have some non-special ed. classes. Â Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Â Also, by now his lack of friends was really hurting him.

 He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself.  I got a> call to come to the school immediately.  We talked with his case manager and I took our son home for a mental health day.  We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist.  He was also in social skills therapy with a social worker, and we brought her in on the problem.  The specialists couldn't really do much about the root of the problem though.  The boy was lonely and you can't *make* other kids accept someone as a friend.  We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved

with their focal interests and ignore each other. Â > > > Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. Â I was still thinking that a 4-year college was a natural choice for such a smart kid. Â The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. Â I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Â Our son's social worker told me that AS kids "crash and burn" in college. Â Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good

conscience grant her the credentials she would need to become a teacher. Â She fell apart (including moving out and> becoming homeless for a while), and her mother was desperately trying to pick up the pieces.> > > We decided to let our son try the high school's technical school. Â Two years later, he has five professional certifications in the computer repair/website design area. Â He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Â Lack of social skills. Â For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Â Also, that executive functioning issue is rearing it's ugly head again. Â He can't really problem solve the way he would need to be able to in a professional

capacity.> > > Then there are the day to day issues. Â He can't remember to take his medicine by himself. Â Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Â Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. Â If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.> > > So here we are. Â He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). Â His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. Â I've had him evaluated by the

Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. Â I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. Â There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. Â I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of> overwhelmed and *he* certainly can't do it himself.> > > This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. Â The social and executive function deficits are *so* much more handicapping than you

think they are when your child is very young.  Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning.  Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.> > > As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future.  It truly is heartbreaking.  I know because we're living it.  My son is still a wonderful person.  He's sweet and innocent in a way that other people aren't.  He's cute.  He's brilliant.  And yet none of that is enough to keep him from having the sort of limited future I could  never have envisioned for him when he was 7yo.> > > I sincerely hope that your experience with AS follows a different pathway from

ours.  It's entirely possible that it will because every person with AS is different from every other person with AS.  I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.> > > Peace.> Sue> > > > > > > The future of our children> Posted by: "" teamjakob06   teamjakob06> Mon Jul 19, 2010 12:48 pm (PDT)> > > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend

college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and> our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. > > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born

and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar! > > >

Link to comment
Share on other sites

Guest guest

Some of the saddest times we've had have been because of people in certain churches. It's pitiful.

We finally found a very accepting church. But,,,,,like you, we realized that spirituality can be felt anywhere. Not just in a church.

God is everywhere.

Attack and enjoy every minute of life.

Try everything.....protect everything.

Robin

From: <teamjakob06>Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 10:27 AM

I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is

another, of course the out come will be different as well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Comtois <suetoiscox (DOT) net> Sent: Tue, July 20, 2010 9:39:05 AMSubject: ( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare

socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering

why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell

apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program

like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06 teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought

of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a

reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

Link to comment
Share on other sites

Guest guest

My son has been accepted at his church for years now. He traveled with them to a church camp in Tennessee (we live in Texas) last summer and he was gone for 8 days. He enjoys going to youth group on Wednesday nights during the school year. It has not translated to friends outside of church or youth group, but he feels accepted and enjoys it so that works for me!

"Over-optimism is waiting for you ship to come in when you haven't sent one out."

From: and/or Robin Lemke <jrisjs@...> Sent: Tue, July 20, 2010 1:33:25 PMSubject: Re: ( ) Re:The future of our children

Some of the saddest times we've had have been because of people in certain churches. It's pitiful.

We finally found a very accepting church. But,,,,,like you, we realized that spirituality can be felt anywhere. Not just in a church.

God is everywhere.

Attack and enjoy every minute of life.

Try everything.. ...protect everything.

Robin

From: <teamjakob06>Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 10:27 AM

I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is

another, of course the out come will be different as well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Comtois <suetoiscox (DOT) net> Sent: Tue, July 20, 2010 9:39:05 AMSubject: ( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare

socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering

why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell

apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program

like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06 teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought

of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a

reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

Link to comment
Share on other sites

Guest guest

Robin...you are right...social skills are very difficult to teach...it is something most kids just easily pick up and learn from the day they are born...it is very very difficult for our children. And, when they do go to classes like your son....they can learn the Ps and Qs but to put it to test in the real world is a whole different story.

My son too went to social classes...he went with kids who were on a lower level ...and they loved playing the games....they just wanted the tokens...and my son was so "bored" ...he just wanted it over. LOL. And, I will never forget....one question was...if your friend was being bulllied would you a. Tell a Teacher b. Ignore it c. Punch the Bully. Guess which one my son picked.....Bingo...he picked C. Punch the Bully. Another questions....if you knew who did such and such...would you a. tell the teacher b. say nothing c. praise the kid.

My son's answer...I'm not going to be a tattletale...

So, it is difficult...and at one point...kids want to fit in with others so they are not going to rat out their "so called" friends. Teaching socializaiton is very very very difficult.

But I will tell you this...I am a Paraprofessional in a school. And, beleive me....I don't look the other way. I don't believe in bullying or teasing ...and I have had teenagers come to me and tell me what is going on or asking me to walk them to the lunch room. It is one area I don't tolerate...and will not tolerate...and the child doesn't just have to have AS or any other dx....I beleive kindness goes a long long way and will continue as long as I am alive to teach it ..

A saying I learned from poppy....It doesn't cost a dime to smile. And if you smile at someone...it becomes contagious....a smile and a wave goes a long long way.

Jan

"In the Midst of Difficulty lies Opportunity" Albert Einstein

Success is not measured by one's position but by the obstacles one has overcome to obtain that position

From: and/or Robin Lemke <jrisjs@...> Sent: Tue, July 20, 2010 1:56:58 PMSubject: Re: ( ) Re:The future of our children

I agree with where schools' emphasis' are.

But,,,,,,,how do you teach to socially fit? Yep, I know that there are groups and classes, but for us, they weren't worth a dime. I remember Ian had Social Skills Class 1 time per week for 20 mins. This was also when the school had thier Assembly's. Ugh.

I may get beat up for this, but I think our kids can learn HOW to react socially but it will NEVER flow naturally. My son addresses everyone. Can say, "Fine thanks, how are you?", but it isn't "natural, if that makes sense.

I think the world would be better off to "get" those darned kids who haven't been taught to be nice. To get the kids that would rather get a laugh than to include others. Shame, also, on the teachers who look the other way or won't / can't jump in and make them be nice.

It's so simple, isn't it? hee hee. I wish.

Attack and enjoy every minute of life.

Try everything.. ...protect everything.

Robin

From: Mimi <suelowerydesign (DOT) com>Subject: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 12:21 PM

Ah ha! I think that you are so right. The social skill aspect is a large part of the equation. Someone on here used to sign their posts "Normal is just a cycle on a washing machine." I loved that quote. And therefore I say, "IQ is just a number." It is not a predictor of outcome, or success or failure in any case. In my limited observation, and I don't want to generalize, there are many kids with disabilities that are not part of the spectrum who are loved by everyone around them! They have the kind of social skills that make other kids take them under their wing, befriend them, want to protect them. Maybe not socialize with them...However, many of our kids do not have these personality traits. They say or do the wrong things, or have inappropriate reactions and poor social skills. In the long run, that, in my opinion only, is what is the biggest factor for success. So tell me why we put so much more emphasis on academic tutoring, help etc

and less on this when they are in school! We have it backwards.Sue in Tn> > > From: <teamjakob06@ ...>> Subject: Re: ( ) Re:The future of our children> > Date: Tuesday, July 20, 2010, 10:27 AM> > >  > > > > > > > I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we

have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is another, of course the out come will be> different as well as how the child{ren} our

raise and how they are involved with their community {church, neighborhood, etc.}.  >  TeamJakob> Support children with > Aspergers,> With your support their is > no limit to Jakob's success!! > > > > > > > From: Comtois <suetoiscox (DOT) net>> > Sent: Tue, July 20, 2010 9:39:05 AM> Subject: ( ) Re:The future of our children> >  > > > I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children.  And I hope you're right.  I hope what you're doing with your son will head off the many problems that develop as these children get older.  We have three sons with AS.  The oldest is 19.  The other two are 15 and 12.  The 15 yo is less affected,

and will, I think, have a relatively normal future.  The 19 yo and the 12 yo are facing a different set of challenges.  > > > When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him.  There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental.  He also had a friend and we had just learned that his verbal IQ was/is about 200.  He taught himself to read grown-up novels shortly after his third birthday.  He was truly brilliant.  I was envisioning a future for him that might include being an author or a college professor.  You know, quirky, but brilliant. > > > When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids.  The biggest problem for my

son was that he eventually lost contact with that one friend he had (and has never been able to make another one).> > > At 8yo he was moved to a full-time gifted program. Â I was so proud of him and it just reinforced my hopes for his future. Â AS wasn't going to stand in the way of anything for my son. Â It wasn't going to be an excuse for a failure to achieve. Â Yeay! Â Unfortunately, a gifted program involves lots of transitions all the time. Â The typical gifted children thrived, but my son was totally overwhelmed. Â The day came when the principal told us that if we brought him back to school the next day, he would expel him. Â I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. Â He did

*wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. Â The school> agreed, and, again, I was hopeful that things were back on track for a successful future.> > > Middle school was a mess. Â He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. Â The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Â Well, so much for that brilliant academic future. Â LD classes don't move as quickly as even general ed. classes for obvious reasons.> > > High school rolled around, and my son got a wonderful case

manager who took a personal interest in him. Â He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. Â But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. Â You see he has executive functioning deficits. Â Keeping himself as organized as a typical high school student is literally impossible for him. Â Where could he get more help with staying organized? Â The LD classes. Â He did, however, have some non-special ed. classes. Â Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Â Also, by now his lack of friends was really hurting him. Â He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. Â I

got a> call to come to the school immediately. Â We talked with his case manager and I took our son home for a mental health day. Â We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. Â He was also in social skills therapy with a social worker, and we brought her in on the problem. Â The specialists couldn't really do much about the root of the problem though. Â The boy was lonely and you can't *make* other kids accept someone as a friend. Â We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other. Â > > > Skipping forward a couple of years, we found

that it was time to start thinking about what our son would do when he finished high school. Â I was still thinking that a 4-year college was a natural choice for such a smart kid. Â The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. Â I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Â Our son's social worker told me that AS kids "crash and burn" in college. Â Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. Â She fell apart (including moving out and>

becoming homeless for a while), and her mother was desperately trying to pick up the pieces.> > > We decided to let our son try the high school's technical school. Â Two years later, he has five professional certifications in the computer repair/website design area. Â He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Â Lack of social skills. Â For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Â Also, that executive functioning issue is rearing it's ugly head again. Â He can't really problem solve the way he would need to be able to in a professional capacity.> > > Then there are the day to day issues. Â He can't remember to take his medicine by himself.

 Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future.  Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth.  If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.> > > So here we are.  He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that).  His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible.  I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him

hired on at Mc's to sweep the floor. Â I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. Â There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. Â I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of> overwhelmed and *he* certainly can't do it himself.> > > This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. Â The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Â Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high

functioning.  Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.> > > As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future.  It truly is heartbreaking.  I know because we're living it.  My son is still a wonderful person.  He's sweet and innocent in a way that other people aren't.  He's cute.  He's brilliant.  And yet none of that is enough to keep him from having the sort of limited future I could  never have envisioned for him when he was 7yo.> > > I sincerely hope that your experience with AS follows a different pathway from ours.  It's entirely possible that it will because every person with AS is different from every other person with AS.  I'm

just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.> > > Peace.> Sue> > > > > > > The future of our children> Posted by: "" teamjakob06   teamjakob06> Mon Jul 19, 2010 12:48 pm (PDT)> > > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may

very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and> our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. > > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL

SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar! > > >

Link to comment
Share on other sites

Guest guest

Hi Robin,

this is the exact message I'm trying to get our school to see. even professionals in sped ed get caught up in this and it takes a lot to get them to understand. I had to say "stop focusing" on his high grades and take a look at the supports needed to get there! nope, that didn't work either. they wanted to take him off the IEP because of his high grades. Until I had to e-mail the teacher everytime he didn't get all information - like coping his notes. had missing info and after several e-mails asking to check on his notes, the sped ed teacher had to start giving him a printed copy of the notes so he would have them. (got her to see that) also got her to see how often that was happening because she missed it!

in the agenda, missing - incomplete homework assignments which brought his grade down because he didn't do his homework because he didn't know he had homework due to having incomplete notes in his agenda or didn't have enough or any information written to know what to do. again, lots of e-mails on that and the sped ed teacher had to check his agenda each day before leaving school. she also had to write in the missing information - almost every day... then there was the poor organization - missing papers, test, homework, papers that had to be signed. they take points off for that too. so the sped ed teacher had to assist him with organizing his binder then put all those papers put into the right subject space. see where this is going? She missed all that because she was focusing on his high grades. you put all this support/help from the sped ed teacher and myself to catch

it and send in those e-mails - you get to see in writing how much assistance is needed and how often. boy does that make a difference and don't feel bad about sending in so many e-mails. because that is their wake up call so they can see in writing how often this is happening. this also shows them that because the child is so high functioning that he's not just being lazy and not doing it. it's because he can't and needs those supports to get it done.

this is so right what you are saying - even professionals miss it - when a child is so high function everything important gets missed when you only focus on the high end. It's great to appreciate the Higher end of the spectrum but when you stop looking at that for a moment and look at everything else you will see a hugh concern. if not corrected in the lower grades the problem doesn't go away. our kids don't learn from mistakes or by watching others and correct the problem themselves. instead they will repeat the problem until someone shows them the correct way. my point - looking at the high grades only or the high functioning part of the autism is so misleading because you miss all the important stuff that's needed to get into college, to go on a job interview, to make good choices (common sense, generalizing,. these things autism kids don't pick up on their own. MOST have to be taught, socialized, maybe

roll played to learn them...

Rose

From: and/or Robin Lemke <jrisjs@...> Sent: Tue, July 20, 2010 12:20:26 PMSubject: Re: ( ) Re:The future of our children

I think the problems become more intense when the child gets into homework. Yes, our kids are smart......some may have really high IQ's, but when organization and homework starts to come into play....that' s where the crap starts to hit the fan.

We, as parents, couldn't understand why, like you now, our kid is struggling. Having breakdowns,, ,,,,,starting to freak out over things that should be so simple. Academics.

The problem for us was when he got a bit older, as many have stated, and socially, they don't fit. Then,,,,when they realize it - it sucks. It can bring out anger and depression and frustrations. You see your kid differently. It crushes you to the core. SEEING that they are different and they they may have to go on a course you honestly didnt' ever see them on because they "were so smart". Hugs to you.

Attack and enjoy every minute of life.

Try everything.. ...protect everything.

Robin

From: <teamjakob06>Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 10:27 AM

I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is

another, of course the out come will be different as well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Comtois <suetoiscox (DOT) net> Sent: Tue, July 20, 2010 9:39:05 AMSubject: ( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare

socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering

why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell

apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program

like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06 teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought

of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a

reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

Link to comment
Share on other sites

Guest guest

Robin,

again you are right! while I've been working in places that have young adults that need job coaches - there is a hugh problem with the social stuff. they need the job coach because they need help with getting a job. the job coach speaks for them. I mean they make the phone calls to see if there is a spot in the job for their client and they go out on the job interview with them. when there is a problem at the job the boss calls the job coach because the client doesn't know how to problem solve and work things out. You know, its just like when in school when NT children use our kids as a targets when they see they are different. they provoke and blame and our kids get caught because they don't know how to speak up for themselves. Same in the working place. when something goes wrong, gets who is at fault...then the job coach gets called in and guess who gets spoken

too...but they are smart, got good grades in school, some can even drive a car but the common sense stuff hits them like a brick wall...listening to them you wonder why they don't have a better paying job - wondering why they are working there doing the type of job they are doing. BUT, when you watch them at work and working with a group of people - you'll understand.

just like in school when your child was in 1st or 2nd grade. you wanted to find out what the problem was so you volunteered in his/her classroom and you saw. the same with young adults. go to a job site that hires adults with disabilities that have a job coach and you'll see their struggles. you can learn so much and understand more on what to help your child with now while he/she is young...you posted it very nice in this post....

Rose

From: and/or Robin Lemke <jrisjs@...> Sent: Tue, July 20, 2010 12:24:27 PMSubject: Re: ( ) Re:The future of our children

I also wanted to say that, if a child is social - they can make it anywhere. Even without academic ability. Sure, their job choice may be limited...but they'll figure it all out.

If a child struggles (or can't do it) socially, therein lies the problem. All the academics in the world isn't going to open the door for them (in most cases). They stilll have to get through an interview.

****

Also,,,,,,as far as being involved with a community or even a church. For many, church has been a place of NOT being accepted. Community has been where we have SEEN that not only does our kid not fit, but it means that WE have lost out, too, on social moments. It's sad.

I hope you never get there.

Attack and enjoy every minute of life.

Try everything.. ...protect everything.

Robin

From: <teamjakob06>Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 10:27 AM

I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is

another, of course the out come will be different as well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Comtois <suetoiscox (DOT) net> Sent: Tue, July 20, 2010 9:39:05 AMSubject: ( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare

socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering

why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell

apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program

like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06 teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought

of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a

reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

Link to comment
Share on other sites

Guest guest

Very well said Rose...and very true...

Keep on plugging...and your son will do well.

jan

"In the Midst of Difficulty lies Opportunity" Albert Einstein

Success is not measured by one's position but by the obstacles one has overcome to obtain that position

From: Rose <beachbodytan2002@...> Sent: Wed, July 21, 2010 8:33:15 AMSubject: Re: ( ) Re:The future of our children

Hi Robin,

this is the exact message I'm trying to get our school to see. even professionals in sped ed get caught up in this and it takes a lot to get them to understand. I had to say "stop focusing" on his high grades and take a look at the supports needed to get there! nope, that didn't work either. they wanted to take him off the IEP because of his high grades. Until I had to e-mail the teacher everytime he didn't get all information - like coping his notes. had missing info and after several e-mails asking to check on his notes, the sped ed teacher had to start giving him a printed copy of the notes so he would have them. (got her to see that) also got her to see how often that was happening because she missed it!

in the agenda, missing - incomplete homework assignments which brought his grade down because he didn't do his homework because he didn't know he had homework due to having incomplete notes in his agenda or didn't have enough or any information written to know what to do. again, lots of e-mails on that and the sped ed teacher had to check his agenda each day before leaving school. she also had to write in the missing information - almost every day... then there was the poor organization - missing papers, test, homework, papers that had to be signed. they take points off for that too. so the sped ed teacher had to assist him with organizing his binder then put all those papers put into the right subject space. see where this is going? She missed all that because she was focusing on his high grades. you put all this support/help from the sped ed teacher and myself to catch

it and send in those e-mails - you get to see in writing how much assistance is needed and how often. boy does that make a difference and don't feel bad about sending in so many e-mails. because that is their wake up call so they can see in writing how often this is happening. this also shows them that because the child is so high functioning that he's not just being lazy and not doing it. it's because he can't and needs those supports to get it done.

this is so right what you are saying - even professionals miss it - when a child is so high function everything important gets missed when you only focus on the high end. It's great to appreciate the Higher end of the spectrum but when you stop looking at that for a moment and look at everything else you will see a hugh concern. if not corrected in the lower grades the problem doesn't go away. our kids don't learn from mistakes or by watching others and correct the problem themselves. instead they will repeat the problem until someone shows them the correct way. my point - looking at the high grades only or the high functioning part of the autism is so misleading because you miss all the important stuff that's needed to get into college, to go on a job interview, to make good choices (common sense, generalizing, . these things autism kids don't pick up on their own. MOST have to be taught, socialized, maybe

roll played to learn them...

Rose

From: and/or Robin Lemke <jrisjs (DOT) com> Sent: Tue, July 20, 2010 12:20:26 PMSubject: Re: ( ) Re:The future of our children

I think the problems become more intense when the child gets into homework. Yes, our kids are smart......some may have really high IQ's, but when organization and homework starts to come into play....that' s where the crap starts to hit the fan.

We, as parents, couldn't understand why, like you now, our kid is struggling. Having breakdowns,, ,,,,,starting to freak out over things that should be so simple. Academics.

The problem for us was when he got a bit older, as many have stated, and socially, they don't fit. Then,,,,when they realize it - it sucks. It can bring out anger and depression and frustrations. You see your kid differently. It crushes you to the core. SEEING that they are different and they they may have to go on a course you honestly didnt' ever see them on because they "were so smart". Hugs to you.

Attack and enjoy every minute of life.

Try everything.. ...protect everything.

Robin

From: <teamjakob06>Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 10:27 AM

I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is

another, of course the out come will be different as well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Comtois <suetoiscox (DOT) net> Sent: Tue, July 20, 2010 9:39:05 AMSubject: ( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare

socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering

why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell

apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program

like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06 teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought

of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a

reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

Link to comment
Share on other sites

Guest guest

For the first time I have read something that sounds similar to my 7 year old. Your describtion of your son loving animals and knowing all about them, gets angry at peers for wrong doin or hurting someone, and yelling across the room at the teacher, these are all things that my child does. His frustration comes out as "God doesn't like it when you do this or that" and strangely in the past, people who have hurt him or been mean have apologized as soon as he blurts out those words in frustration. They may be scared of him or his words may have just been that powerful.

I know we all are fighting for our children everyday. I have family members who don't even come around because of him, but thats okay, who needs them. The new song "King of Anything", is a great song for all our children! Put it in YouTube and listen to it. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: and/or Robin Lemke <jrisjs@...> Sent: Tue, July 20, 2010 12:54:09 PMSubject: Re: ( ) Re:The future of our children

I'm so sorry that this has turned out like this.

No one wants to make anyone angry or insult anyone.

No one wants you to apologize for wanting what's best for your son or for fighting to ensure he becomes all that he can be.

We're all there. We're all doing it.

No one has ever just given up or set lower bars. We've just, as our kids have gotten closer to adulthood, seen what our kids can do and can handle. That's it.

We all fight for them. At school, in the community, amongst neighbors, in stores, with doctors, in libraries, at the YMCA, on the street, in movie theaters, with other kids' families, with our own families, at church, and even amongst ourselves.

Eventually, time flies and you have a teenager. Not a child who can be made to play nice. Not a child who you are "teaching" how to behave. You have a kid who knows what he wants. Who is physically grown and age-wise, is a young man or woman. But,,,that no one wants around. Or that you have to fight the school to PROVE that although they are brilliant, they can't figure out how to get their locker open. Or that you have to, as some here have stated, have them leave a class early just to avoid confusion and stress, to get to their next class.

I've got a kid who can read all day long. Figures out math in his head........ love to take care of animals and knows everything about them. Can talk to people at church, impresses the crap out of them,,,,,,,but if he goes to the pool and see's some kids playing catch with a ball, and the ball smacks one of the players in the face (on accident/fun) , he'll get angry that it happened and will show obvious anger and frustration.

He can do what you ask, finish his work, be an honest-go-God angel but will holler across the gym in class to his teacher to ask her if he can go to the bathroom. (He's 14).

S0........this is where the other comments are coming from. Our hearts. Our hurt. Our experience.

Not that you'll go through the exact same stuff....you won't.

But,,,,hearing about "not allowing him to sit behind closed doors" or "being afraid" and not "lowing the bar" is not what any of us are doing. We are living our realities as they are right now.....for our kids....whatever their ages. Just as you are.

In all honestly, I think that my son has more confidence that most. He doesn't hide here. He simply is happy with the way things are. He likes himself. A lot.

So, please accept our posts as they are meant. Just as we will accept yours. We all have good intentions. Our emotions just get in the way sometimes.

Attack and enjoy every minute of life.

Try everything.. ...protect everything.

Robin

From: <teamjakob06>Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 10:45 AM

There is no need for anyone to be angry because the bottom line is that I refuse to hide my child behind close doors for fear of what other people may say or think. I will not allow him to sit alone in his room scared of the world! All I have left to say is that the world better get ready for Jakob because he will concur all things through our Lord, Jesus Christ and that is all that matters! If your upset, I'm sorry, but I am not apologizing for what I said, just simply that it made you upset. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Mimi <suelowerydesign (DOT) com> Sent: Tue, July 20, 2010 10:40:09 AMSubject: ( ) Re:The future of our children

Thank you. Thank you. Thank you. You expressed beautifully what I was too upset and angry to say, I am glad you did not cut a single word.Sue in TN>> I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges. > > When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him.

There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant. > > When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).> > At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going

to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.> > Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same

district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.> > High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying

organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped

that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other. > > Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty

informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.> > We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't

really problem solve the way he would need to be able to in a professional capacity.> > Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.> > So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the

Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.> > This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also,

children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.> > As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.> > I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be

careful about judging other parents because you could so easily be walking in their shoes in ten years.> > Peace.> Sue> > > > The future of our children> > Posted by: "" teamjakob06@ ... teamjakob06> > Mon Jul 19, 2010 12:48 pm (PDT)> > > > > > > > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I

look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. > > > > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have

to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar! > > > > >

Link to comment
Share on other sites

Guest guest

I see that we have 2 choices here.... Somehow help our children learn to become socialized or allow them to be like the 2 guys in the movie "Step Brothers", which if you haven't seen yet, watch the rated verison. But its basically about 2 grown men who become step brothers and still live at home with their parents and well it goes on to be one hillarious movie, but they {the parents} evenually realize that their kids are awesome and well you'll just have to watch it to see what happens. BUT WATCH THE RATED VERISON! I had to pray througout the entire movie, but I was asked to watch it and give my opionion, would have been nice to know that they had a rated version.. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Mimi <sue@...> Sent: Tue, July 20, 2010 1:21:36 PMSubject: ( ) Re:The future of our children

Ah ha! I think that you are so right. The social skill aspect is a large part of the equation. Someone on here used to sign their posts "Normal is just a cycle on a washing machine." I loved that quote. And therefore I say, "IQ is just a number." It is not a predictor of outcome, or success or failure in any case. In my limited observation, and I don't want to generalize, there are many kids with disabilities that are not part of the spectrum who are loved by everyone around them! They have the kind of social skills that make other kids take them under their wing, befriend them, want to protect them. Maybe not socialize with them...However, many of our kids do not have these personality traits. They say or do the wrong things, or have inappropriate reactions and poor social skills. In the long run, that, in my opinion only, is what is the biggest factor for success. So tell me why we put so much more emphasis on academic tutoring, help etc and

less on this when they are in school! We have it backwards.Sue in Tn> > > From: <teamjakob06@...>> Subject: Re: ( ) Re:The future of our children> > Date: Tuesday, July 20, 2010, 10:27 AM> > > Â > > > > > > > I personally am not judging anyone, I am only going on what I have read.

Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is another, of course the out come will be> different as

well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}.  >  TeamJakob> Support children with > Aspergers,> With your support their is > no limit to Jakob's success!! > > > > > > > From: Comtois <suetoiscox (DOT) net>> > Sent: Tue, July 20, 2010 9:39:05 AM> Subject: ( ) Re:The future of our children> >  > > > I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children.  And I hope you're right.  I hope what you're doing with your son will head off the many problems that develop as these children get older.  We have three sons with AS.  The oldest is 19.  The other two are 15 and 12.

 The 15 yo is less affected, and will, I think, have a relatively normal future.  The 19 yo and the 12 yo are facing a different set of challenges.  > > > When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him.  There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental.  He also had a friend and we had just learned that his verbal IQ was/is about 200.  He taught himself to read grown-up novels shortly after his third birthday.  He was truly brilliant.  I was envisioning a future for him that might include being an author or a college professor.  You know, quirky, but brilliant. > > > When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids.

 The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).> > > At 8yo he was moved to a full-time gifted program.  I was so proud of him and it just reinforced my hopes for his future.  AS wasn't going to stand in the way of anything for my son.  It wasn't going to be an excuse for a failure to achieve.  Yeay!  Unfortunately, a gifted program involves lots of transitions all the time.  The typical gifted children thrived, but my son was totally overwhelmed.  The day came when the principal told us that if we brought him back to school the next day, he would expel him.  I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning

coping mechanisms. Â He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. Â The school> agreed, and, again, I was hopeful that things were back on track for a successful future.> > > Middle school was a mess. Â He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. Â The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Â Well, so much for that brilliant academic future. Â LD classes don't move as quickly as even general ed. classes for obvious reasons.> > > High school rolled around, and

my son got a wonderful case manager who took a personal interest in him. Â He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. Â But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. Â You see he has executive functioning deficits. Â Keeping himself as organized as a typical high school student is literally impossible for him. Â Where could he get more help with staying organized? Â The LD classes. Â He did, however, have some non-special ed. classes. Â Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Â Also, by now his lack of friends was really hurting him. Â He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't

just kill himself. Â I got a> call to come to the school immediately. Â We talked with his case manager and I took our son home for a mental health day. Â We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. Â He was also in social skills therapy with a social worker, and we brought her in on the problem. Â The specialists couldn't really do much about the root of the problem though. Â The boy was lonely and you can't *make* other kids accept someone as a friend. Â We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other. Â > > > Skipping forward a

couple of years, we found that it was time to start thinking about what our son would do when he finished high school. Â I was still thinking that a 4-year college was a natural choice for such a smart kid. Â The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. Â I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Â Our son's social worker told me that AS kids "crash and burn" in college. Â Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. Â She fell apart

(including moving out and> becoming homeless for a while), and her mother was desperately trying to pick up the pieces.> > > We decided to let our son try the high school's technical school. Â Two years later, he has five professional certifications in the computer repair/website design area. Â He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Â Lack of social skills. Â For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Â Also, that executive functioning issue is rearing it's ugly head again. Â He can't really problem solve the way he would need to be able to in a professional capacity.> > > Then there are the day to day issues. Â He can't remember to take his

medicine by himself. Â Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Â Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. Â If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.> > > So here we are. Â He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). Â His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. Â I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that

means they'll get him hired on at Mc's to sweep the floor. Â I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. Â There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. Â I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of> overwhelmed and *he* certainly can't do it himself.> > > This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. Â The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Â Also, children who can be diagnosed at 5 or 6 yo probably

*aren't* all that high functioning.  Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.> > > As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future.  It truly is heartbreaking.  I know because we're living it.  My son is still a wonderful person.  He's sweet and innocent in a way that other people aren't.  He's cute.  He's brilliant.  And yet none of that is enough to keep him from having the sort of limited future I could  never have envisioned for him when he was 7yo.> > > I sincerely hope that your experience with AS follows a different pathway from ours.  It's entirely possible that it will because every person with AS is different from every other person

with AS.  I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.> > > Peace.> Sue> > > > > > > The future of our children> Posted by: "" teamjakob06   teamjakob06> Mon Jul 19, 2010 12:48 pm (PDT)> > > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special

college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and> our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. > > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T

RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar! > > >

Link to comment
Share on other sites

Guest guest

I have had situations like that and saddly my sister in law was his Sunday school teacher. I switched to my parents church and well now he practically teaches the class, which the Sunday school teacher thinks is fabulous. But I had to search for a church, not anyone would work, it had to be the one! TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: or Sandee Culliton <jculliton@...> Sent: Tue, July 20, 2010 1:23:48 PMSubject: Re: ( ) Re:The future of our children

 As far as church goes. I am with Robin.. I have never felt so unaccepted as when I attempted church with my kids. With my son's age group there was a little old lady who gave out candy to all the "good " kids after Sunday School . Of course, she always left my kids out since they were not "good" (meaning quiet). When I tried again with my granddaughter, it went ok until the day they introduced loud music to the program, and she wouldn't participate and, again, the little old lady that was the class "shepherd" screamed across the whole Sunday School gathering that "That girl needs therapy!" and later explained that she was only trying to let us know that she is in deep need of help. She harrassed several other kids, too, but my husband would no longer attend church, nor my daughter and I have quit trying too. I talk to God at home.

( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare

socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering

why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell

apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program

like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06 teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought

of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a

reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

Link to comment
Share on other sites

Guest guest

...our children have all the choices in the world....we just need to stand by them...help them, nurture them, assist in every way possible....pray and know that in the end....God will take care...he has a plan.

"In the Midst of Difficulty lies Opportunity" Albert Einstein

Success is not measured by one's position but by the obstacles one has overcome to obtain that position

From: <teamjakob06@...> Sent: Wed, July 21, 2010 9:03:01 AMSubject: Re: ( ) Re:The future of our children

I see that we have 2 choices here.... Somehow help our children learn to become socialized or allow them to be like the 2 guys in the movie "Step Brothers", which if you haven't seen yet, watch the rated verison. But its basically about 2 grown men who become step brothers and still live at home with their parents and well it goes on to be one hillarious movie, but they {the parents} evenually realize that their kids are awesome and well you'll just have to watch it to see what happens. BUT WATCH THE RATED VERISON! I had to pray througout the entire movie, but I was asked to watch it and give my opionion, would have been nice to know that they had a rated version.. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Mimi <suelowerydesign (DOT) com> Sent: Tue, July 20, 2010 1:21:36 PMSubject: ( ) Re:The future of our children

Ah ha! I think that you are so right. The social skill aspect is a large part of the equation. Someone on here used to sign their posts "Normal is just a cycle on a washing machine." I loved that quote. And therefore I say, "IQ is just a number." It is not a predictor of outcome, or success or failure in any case. In my limited observation, and I don't want to generalize, there are many kids with disabilities that are not part of the spectrum who are loved by everyone around them! They have the kind of social skills that make other kids take them under their wing, befriend them, want to protect them. Maybe not socialize with them...However, many of our kids do not have these personality traits. They say or do the wrong things, or have inappropriate reactions and poor social skills. In the long run, that, in my opinion only, is what is the biggest factor for success. So tell me why we put so much more emphasis on academic tutoring, help etc and

less on this when they are in school! We have it backwards.Sue in Tn> > > From: <teamjakob06@ ...>> Subject: Re: ( ) Re:The future of our children> > Date: Tuesday, July 20, 2010, 10:27 AM> > > Â > > > > > > > I personally am not judging anyone, I am only going on what I have read.

Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is another, of course the out come will be> different as

well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}.  >  TeamJakob> Support children with > Aspergers,> With your support their is > no limit to Jakob's success!! > > > > > > > From: Comtois <suetoiscox (DOT) net>> > Sent: Tue, July 20, 2010 9:39:05 AM> Subject: ( ) Re:The future of our children> >  > > > I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children.  And I hope you're right.  I hope what you're doing with your son will head off the many problems that develop as these children get older.  We have three sons with AS.  The oldest is 19.  The other two are 15 and 12.

 The 15 yo is less affected, and will, I think, have a relatively normal future.  The 19 yo and the 12 yo are facing a different set of challenges.  > > > When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him.  There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental.  He also had a friend and we had just learned that his verbal IQ was/is about 200.  He taught himself to read grown-up novels shortly after his third birthday.  He was truly brilliant.  I was envisioning a future for him that might include being an author or a college professor.  You know, quirky, but brilliant. > > > When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids.

 The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).> > > At 8yo he was moved to a full-time gifted program.  I was so proud of him and it just reinforced my hopes for his future.  AS wasn't going to stand in the way of anything for my son.  It wasn't going to be an excuse for a failure to achieve.  Yeay!  Unfortunately, a gifted program involves lots of transitions all the time.  The typical gifted children thrived, but my son was totally overwhelmed.  The day came when the principal told us that if we brought him back to school the next day, he would expel him.  I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning

coping mechanisms. Â He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. Â The school> agreed, and, again, I was hopeful that things were back on track for a successful future.> > > Middle school was a mess. Â He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. Â The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Â Well, so much for that brilliant academic future. Â LD classes don't move as quickly as even general ed. classes for obvious reasons.> > > High school rolled around, and

my son got a wonderful case manager who took a personal interest in him. Â He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. Â But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. Â You see he has executive functioning deficits. Â Keeping himself as organized as a typical high school student is literally impossible for him. Â Where could he get more help with staying organized? Â The LD classes. Â He did, however, have some non-special ed. classes. Â Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Â Also, by now his lack of friends was really hurting him. Â He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't

just kill himself. Â I got a> call to come to the school immediately. Â We talked with his case manager and I took our son home for a mental health day. Â We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. Â He was also in social skills therapy with a social worker, and we brought her in on the problem. Â The specialists couldn't really do much about the root of the problem though. Â The boy was lonely and you can't *make* other kids accept someone as a friend. Â We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other. Â > > > Skipping forward a

couple of years, we found that it was time to start thinking about what our son would do when he finished high school. Â I was still thinking that a 4-year college was a natural choice for such a smart kid. Â The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. Â I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Â Our son's social worker told me that AS kids "crash and burn" in college. Â Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. Â She fell apart

(including moving out and> becoming homeless for a while), and her mother was desperately trying to pick up the pieces.> > > We decided to let our son try the high school's technical school. Â Two years later, he has five professional certifications in the computer repair/website design area. Â He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Â Lack of social skills. Â For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Â Also, that executive functioning issue is rearing it's ugly head again. Â He can't really problem solve the way he would need to be able to in a professional capacity.> > > Then there are the day to day issues. Â He can't remember to take his

medicine by himself. Â Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Â Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. Â If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.> > > So here we are. Â He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). Â His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. Â I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that

means they'll get him hired on at Mc's to sweep the floor. Â I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. Â There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. Â I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of> overwhelmed and *he* certainly can't do it himself.> > > This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. Â The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Â Also, children who can be diagnosed at 5 or 6 yo probably

*aren't* all that high functioning.  Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.> > > As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future.  It truly is heartbreaking.  I know because we're living it.  My son is still a wonderful person.  He's sweet and innocent in a way that other people aren't.  He's cute.  He's brilliant.  And yet none of that is enough to keep him from having the sort of limited future I could  never have envisioned for him when he was 7yo.> > > I sincerely hope that your experience with AS follows a different pathway from ours.  It's entirely possible that it will because every person with AS is different from every other person

with AS.  I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.> > > Peace.> Sue> > > > > > > The future of our children> Posted by: "" teamjakob06   teamjakob06> Mon Jul 19, 2010 12:48 pm (PDT)> > > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a

special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and> our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. > > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help,

BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar! > > >

Link to comment
Share on other sites

Guest guest

If you want to watch a movie...watch Adam....it was very good...much better than half-brothers...although my son laughed his head off at half-brothers...Adam is much better.

"In the Midst of Difficulty lies Opportunity" Albert Einstein

Success is not measured by one's position but by the obstacles one has overcome to obtain that position

From: <teamjakob06@...> Sent: Wed, July 21, 2010 8:54:38 AMSubject: Re: ( ) Re:The future of our children

For the first time I have read something that sounds similar to my 7 year old. Your describtion of your son loving animals and knowing all about them, gets angry at peers for wrong doin or hurting someone, and yelling across the room at the teacher, these are all things that my child does. His frustration comes out as "God doesn't like it when you do this or that" and strangely in the past, people who have hurt him or been mean have apologized as soon as he blurts out those words in frustration. They may be scared of him or his words may have just been that powerful.

I know we all are fighting for our children everyday. I have family members who don't even come around because of him, but thats okay, who needs them. The new song "King of Anything", is a great song for all our children! Put it in YouTube and listen to it. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: and/or Robin Lemke <jrisjs (DOT) com> Sent: Tue, July 20, 2010 12:54:09 PMSubject: Re: ( ) Re:The future of our children

I'm so sorry that this has turned out like this.

No one wants to make anyone angry or insult anyone.

No one wants you to apologize for wanting what's best for your son or for fighting to ensure he becomes all that he can be.

We're all there. We're all doing it.

No one has ever just given up or set lower bars. We've just, as our kids have gotten closer to adulthood, seen what our kids can do and can handle. That's it.

We all fight for them. At school, in the community, amongst neighbors, in stores, with doctors, in libraries, at the YMCA, on the street, in movie theaters, with other kids' families, with our own families, at church, and even amongst ourselves.

Eventually, time flies and you have a teenager. Not a child who can be made to play nice. Not a child who you are "teaching" how to behave. You have a kid who knows what he wants. Who is physically grown and age-wise, is a young man or woman. But,,,that no one wants around. Or that you have to fight the school to PROVE that although they are brilliant, they can't figure out how to get their locker open. Or that you have to, as some here have stated, have them leave a class early just to avoid confusion and stress, to get to their next class.

I've got a kid who can read all day long. Figures out math in his head........ love to take care of animals and knows everything about them. Can talk to people at church, impresses the crap out of them,,,,,,,but if he goes to the pool and see's some kids playing catch with a ball, and the ball smacks one of the players in the face (on accident/fun) , he'll get angry that it happened and will show obvious anger and frustration.

He can do what you ask, finish his work, be an honest-go-God angel but will holler across the gym in class to his teacher to ask her if he can go to the bathroom. (He's 14).

S0........this is where the other comments are coming from. Our hearts. Our hurt. Our experience.

Not that you'll go through the exact same stuff....you won't.

But,,,,hearing about "not allowing him to sit behind closed doors" or "being afraid" and not "lowing the bar" is not what any of us are doing. We are living our realities as they are right now.....for our kids....whatever their ages. Just as you are.

In all honestly, I think that my son has more confidence that most. He doesn't hide here. He simply is happy with the way things are. He likes himself. A lot.

So, please accept our posts as they are meant. Just as we will accept yours. We all have good intentions. Our emotions just get in the way sometimes.

Attack and enjoy every minute of life.

Try everything.. ...protect everything.

Robin

From: <teamjakob06>Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 10:45 AM

There is no need for anyone to be angry because the bottom line is that I refuse to hide my child behind close doors for fear of what other people may say or think. I will not allow him to sit alone in his room scared of the world! All I have left to say is that the world better get ready for Jakob because he will concur all things through our Lord, Jesus Christ and that is all that matters! If your upset, I'm sorry, but I am not apologizing for what I said, just simply that it made you upset. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Mimi <suelowerydesign (DOT) com> Sent: Tue, July 20, 2010 10:40:09 AMSubject: ( ) Re:The future of our children

Thank you. Thank you. Thank you. You expressed beautifully what I was too upset and angry to say, I am glad you did not cut a single word.Sue in TN>> I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges. > > When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him.

There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant. > > When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).> > At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going

to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.> > Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same

district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.> > High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying

organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped

that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other. > > Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty

informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.> > We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't

really problem solve the way he would need to be able to in a professional capacity.> > Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.> > So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the

Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.> > This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also,

children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.> > As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.> > I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be

careful about judging other parents because you could so easily be walking in their shoes in ten years.> > Peace.> Sue> > > > The future of our children> > Posted by: "" teamjakob06@ ... teamjakob06> > Mon Jul 19, 2010 12:48 pm (PDT)> > > > > > > > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I

look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. > > > > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have

to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar! > > > > >

Link to comment
Share on other sites

Guest guest

Well said, woman. Your Poppy was a good man.

Attack and enjoy every minute of life.

Try everything.....protect everything.

Robin

From: Mimi <suelowerydesign (DOT) com>Subject: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 12:21 PM

Ah ha! I think that you are so right. The social skill aspect is a large part of the equation. Someone on here used to sign their posts "Normal is just a cycle on a washing machine." I loved that quote. And therefore I say, "IQ is just a number." It is not a predictor of outcome, or success or failure in any case. In my limited observation, and I don't want to generalize, there are many kids with disabilities that are not part of the spectrum who are loved by everyone around them! They have the kind of social skills that make other kids take them under their wing, befriend them, want to protect them. Maybe not socialize with them...However, many of our kids do not have these personality traits. They say or do the wrong things, or have inappropriate reactions and poor social skills. In the long run, that, in my opinion only, is what is the biggest factor for success. So tell me why we put so much more emphasis on academic tutoring, help etc

and less on this when they are in school! We have it backwards.Sue in Tn> > > From: <teamjakob06@ ...>> Subject: Re: ( ) Re:The future of our children> > Date: Tuesday, July 20, 2010, 10:27 AM> > >  > > > > > > > I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we

have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is another, of course the out come will be> different as well as how the child{ren} our

raise and how they are involved with their community {church, neighborhood, etc.}.  >  TeamJakob> Support children with > Aspergers,> With your support their is > no limit to Jakob's success!! > > > > > > > From: Comtois <suetoiscox (DOT) net>> > Sent: Tue, July 20, 2010 9:39:05 AM> Subject: ( ) Re:The future of our children> >  > > > I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children.  And I hope you're right.  I hope what you're doing with your son will head off the many problems that develop as these children get older.  We have three sons with AS.  The oldest is 19.  The other two are 15 and 12.  The 15 yo is less affected,

and will, I think, have a relatively normal future.  The 19 yo and the 12 yo are facing a different set of challenges.  > > > When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him.  There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental.  He also had a friend and we had just learned that his verbal IQ was/is about 200.  He taught himself to read grown-up novels shortly after his third birthday.  He was truly brilliant.  I was envisioning a future for him that might include being an author or a college professor.  You know, quirky, but brilliant. > > > When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids.  The biggest problem for my

son was that he eventually lost contact with that one friend he had (and has never been able to make another one).> > > At 8yo he was moved to a full-time gifted program. Â I was so proud of him and it just reinforced my hopes for his future. Â AS wasn't going to stand in the way of anything for my son. Â It wasn't going to be an excuse for a failure to achieve. Â Yeay! Â Unfortunately, a gifted program involves lots of transitions all the time. Â The typical gifted children thrived, but my son was totally overwhelmed. Â The day came when the principal told us that if we brought him back to school the next day, he would expel him. Â I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. Â He did

*wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. Â The school> agreed, and, again, I was hopeful that things were back on track for a successful future.> > > Middle school was a mess. Â He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. Â The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Â Well, so much for that brilliant academic future. Â LD classes don't move as quickly as even general ed. classes for obvious reasons.> > > High school rolled around, and my son got a wonderful case

manager who took a personal interest in him. Â He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. Â But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. Â You see he has executive functioning deficits. Â Keeping himself as organized as a typical high school student is literally impossible for him. Â Where could he get more help with staying organized? Â The LD classes. Â He did, however, have some non-special ed. classes. Â Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Â Also, by now his lack of friends was really hurting him. Â He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. Â I

got a> call to come to the school immediately. Â We talked with his case manager and I took our son home for a mental health day. Â We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. Â He was also in social skills therapy with a social worker, and we brought her in on the problem. Â The specialists couldn't really do much about the root of the problem though. Â The boy was lonely and you can't *make* other kids accept someone as a friend. Â We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other. Â > > > Skipping forward a couple of years, we found

that it was time to start thinking about what our son would do when he finished high school. Â I was still thinking that a 4-year college was a natural choice for such a smart kid. Â The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. Â I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Â Our son's social worker told me that AS kids "crash and burn" in college. Â Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. Â She fell apart (including moving out and>

becoming homeless for a while), and her mother was desperately trying to pick up the pieces.> > > We decided to let our son try the high school's technical school. Â Two years later, he has five professional certifications in the computer repair/website design area. Â He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Â Lack of social skills. Â For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Â Also, that executive functioning issue is rearing it's ugly head again. Â He can't really problem solve the way he would need to be able to in a professional capacity.> > > Then there are the day to day issues. Â He can't remember to take his medicine by himself.

 Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future.  Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth.  If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.> > > So here we are.  He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that).  His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible.  I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him

hired on at Mc's to sweep the floor. Â I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. Â There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. Â I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of> overwhelmed and *he* certainly can't do it himself.> > > This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. Â The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Â Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high

functioning.  Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.> > > As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future.  It truly is heartbreaking.  I know because we're living it.  My son is still a wonderful person.  He's sweet and innocent in a way that other people aren't.  He's cute.  He's brilliant.  And yet none of that is enough to keep him from having the sort of limited future I could  never have envisioned for him when he was 7yo.> > > I sincerely hope that your experience with AS follows a different pathway from ours.  It's entirely possible that it will because every person with AS is different from every other person with AS.  I'm

just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.> > > Peace.> Sue> > > > > > > The future of our children> Posted by: "" teamjakob06   teamjakob06> Mon Jul 19, 2010 12:48 pm (PDT)> > > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college

either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and> our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. > > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON

THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar! > > >

Link to comment
Share on other sites

Guest guest

Perfectly said, Rose. (And I'm shocked at the lack of knowledge of some SPED folk.) Ugh.....

Attack and enjoy every minute of life.

Try everything.....protect everything.

Robin

From: <teamjakob06>Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 10:27 AM

I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is

another, of course the out come will be different as well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Comtois <suetoiscox (DOT) net> Sent: Tue, July 20, 2010 9:39:05 AMSubject: ( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare

socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering

why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell

apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program

like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06 teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought

of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a

reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

Link to comment
Share on other sites

Guest guest

Hee hee. It's amazing that even though our kids are so different, there are incredible similarities!!!!

Attack and enjoy every minute of life.

Try everything.....protect everything.

Robin

From: <teamjakob06>Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 10:45 AM

There is no need for anyone to be angry because the bottom line is that I refuse to hide my child behind close doors for fear of what other people may say or think. I will not allow him to sit alone in his room scared of the world! All I have left to say is that the world better get ready for Jakob because he will concur all things through our Lord, Jesus Christ and that is all that matters! If your upset, I'm sorry, but I am not apologizing for what I said, just simply that it made you upset. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Mimi <suelowerydesign (DOT) com> Sent: Tue, July 20, 2010 10:40:09 AMSubject: ( ) Re:The future of our children

Thank you. Thank you. Thank you. You expressed beautifully what I was too upset and angry to say, I am glad you did not cut a single word.Sue in TN>> I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges. > > When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him.

There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant. > > When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).> > At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going

to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.> > Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same

district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.> > High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying

organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped

that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other. > > Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty

informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.> > We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't

really problem solve the way he would need to be able to in a professional capacity.> > Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.> > So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the

Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.> > This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also,

children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.> > As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.> > I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be

careful about judging other parents because you could so easily be walking in their shoes in ten years.> > Peace.> Sue> > > > The future of our children> > Posted by: "" teamjakob06@ ... teamjakob06> > Mon Jul 19, 2010 12:48 pm (PDT)> > > > > > > > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I

look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. > > > > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have

to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar! > > > > >

Link to comment
Share on other sites

Guest guest

I hope-to-God that there are more than those 2!!! hee hee.

I, personally loved the movie. Naughty version and all. he he.

Anyway, yeah, it does spmetimes seem lilke it's either: 1 - help them change to fit, or 2 - let them be and fail. There's somewhere in the middle....I feel.

I coach him and help him socialize by simply having him be with us and live. But, I don't push it or enroll him in social classes outside of school. (He did go to an Asperger's camp with Easter Seals once and LOVED IT!!!).

I let him live within his comfort zone and be alone (not lonely) when he chooses to, but still correct him and demand that he do his best.

Attack and enjoy every minute of life.

Try everything.....protect everything.

Robin

From: <teamjakob06@...>Subject: Re: ( ) Re:The future of our children Date: Wednesday, July 21, 2010, 8:03 AM

I see that we have 2 choices here.... Somehow help our children learn to become socialized or allow them to be like the 2 guys in the movie "Step Brothers", which if you haven't seen yet, watch the rated verison. But its basically about 2 grown men who become step brothers and still live at home with their parents and well it goes on to be one hillarious movie, but they {the parents} evenually realize that their kids are awesome and well you'll just have to watch it to see what happens. BUT WATCH THE RATED VERISON! I had to pray througout the entire movie, but I was asked to watch it and give my opionion, would have been nice to know that they had a rated version.. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Mimi <suelowerydesign (DOT) com> Sent: Tue, July 20, 2010 1:21:36 PMSubject: ( ) Re:The future of our children

Ah ha! I think that you are so right. The social skill aspect is a large part of the equation. Someone on here used to sign their posts "Normal is just a cycle on a washing machine." I loved that quote. And therefore I say, "IQ is just a number." It is not a predictor of outcome, or success or failure in any case. In my limited observation, and I don't want to generalize, there are many kids with disabilities that are not part of the spectrum who are loved by everyone around them! They have the kind of social skills that make other kids take them under their wing, befriend them, want to protect them. Maybe not socialize with them...However, many of our kids do not have these personality traits. They say or do the wrong things, or have inappropriate reactions and poor social skills. In the long run, that, in my opinion only, is what is the biggest factor for success. So tell me why we put so much more emphasis on academic tutoring, help etc

and less on this when they are in school! We have it backwards.Sue in Tn> > > From: <teamjakob06@ ...>> Subject: Re: ( ) Re:The future of our children> > Date: Tuesday, July 20, 2010, 10:27 AM> > > Â > > > > > >

> I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing

and having more then one is another, of course the out come will be> different as well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}.  >  TeamJakob> Support children with > Aspergers,> With your support their is > no limit to Jakob's success!! > > > > > > > From: Comtois <suetoiscox (DOT) net>> > Sent: Tue, July 20, 2010 9:39:05 AM> Subject: ( ) Re:The future of our children> >  > > > I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children.  And I hope you're right.  I hope what you're doing with your son will head off the many problems that develop as these children get older.

 We have three sons with AS.  The oldest is 19.  The other two are 15 and 12.  The 15 yo is less affected, and will, I think, have a relatively normal future.  The 19 yo and the 12 yo are facing a different set of challenges.  > > > When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him.  There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental.  He also had a friend and we had just learned that his verbal IQ was/is about 200.  He taught himself to read grown-up novels shortly after his third birthday.  He was truly brilliant.  I was envisioning a future for him that might include being an author or a college professor.  You know, quirky, but brilliant. > > > When he was 7 1/2 the military transferred us to a

different state, and we elected to move into a district that had a fabulous program for gifted kids. Â The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).> > > At 8yo he was moved to a full-time gifted program. Â I was so proud of him and it just reinforced my hopes for his future. Â AS wasn't going to stand in the way of anything for my son. Â It wasn't going to be an excuse for a failure to achieve. Â Yeay! Â Unfortunately, a gifted program involves lots of transitions all the time. Â The typical gifted children thrived, but my son was totally overwhelmed. Â The day came when the principal told us that if we brought him back to school the next day, he would expel him. Â I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and

homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. Â He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. Â The school> agreed, and, again, I was hopeful that things were back on track for a successful future.> > > Middle school was a mess. Â He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. Â The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Â Well, so much for that brilliant academic future. Â LD classes don't move as quickly as even

general ed. classes for obvious reasons.> > > High school rolled around, and my son got a wonderful case manager who took a personal interest in him. Â He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. Â But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. Â You see he has executive functioning deficits. Â Keeping himself as organized as a typical high school student is literally impossible for him. Â Where could he get more help with staying organized? Â The LD classes. Â He did, however, have some non-special ed. classes. Â Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Â Also, by now his lack of friends was really hurting him.

 He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself.  I got a> call to come to the school immediately.  We talked with his case manager and I took our son home for a mental health day.  We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist.  He was also in social skills therapy with a social worker, and we brought her in on the problem.  The specialists couldn't really do much about the root of the problem though.  The boy was lonely and you can't *make* other kids accept someone as a friend.  We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved

with their focal interests and ignore each other. Â > > > Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. Â I was still thinking that a 4-year college was a natural choice for such a smart kid. Â The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. Â I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Â Our son's social worker told me that AS kids "crash and burn" in college. Â Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good

conscience grant her the credentials she would need to become a teacher. Â She fell apart (including moving out and> becoming homeless for a while), and her mother was desperately trying to pick up the pieces.> > > We decided to let our son try the high school's technical school. Â Two years later, he has five professional certifications in the computer repair/website design area. Â He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Â Lack of social skills. Â For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Â Also, that executive functioning issue is rearing it's ugly head again. Â He can't really problem solve the way he would need to be able to in a professional

capacity.> > > Then there are the day to day issues. Â He can't remember to take his medicine by himself. Â Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Â Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. Â If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.> > > So here we are. Â He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). Â His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. Â I've had him evaluated by the

Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. Â I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. Â There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. Â I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of> overwhelmed and *he* certainly can't do it himself.> > > This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. Â The social and executive function deficits are *so* much more handicapping than you

think they are when your child is very young.  Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning.  Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.> > > As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future.  It truly is heartbreaking.  I know because we're living it.  My son is still a wonderful person.  He's sweet and innocent in a way that other people aren't.  He's cute.  He's brilliant.  And yet none of that is enough to keep him from having the sort of limited future I could  never have envisioned for him when he was 7yo.> > > I sincerely hope that your experience with AS follows a different pathway from

ours.  It's entirely possible that it will because every person with AS is different from every other person with AS.  I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.> > > Peace.> Sue> > > > > > > The future of our children> Posted by: "" teamjakob06   teamjakob06> Mon Jul 19, 2010 12:48 pm (PDT)> > > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are

endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and> our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. > > We used to live in Georgia and they had very little

resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar! > > >

Link to comment
Share on other sites

Guest guest

I agree. In my heart I believe my daughter has the ability to go places in life (she wants to be a writer, and is already a pretty good one) but I do understand that there will be obstacles and her path may be different than that of her peers. College may not be for her, and if that is the case so be it. I have two grown nephews, one with EFD and one with ADHD and Tourettes. Both started college and left shortly thereafter. But both found their path in life and are doing well and are happy. That is all that matters.So I guess what I would say is that while I am not lowering my expectations of Liz's future, I am being realistic in my expectations of how she might get there. From: sue@...Date: Tue, 20 Jul 2010 14:40:09 +0000Subject: ( ) Re:The future of our children

Thank you. Thank you. Thank you. You expressed beautifully what I was too upset and angry to say, I am glad you did not cut a single word.

Sue in TN

>

> I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

>

> When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

>

> When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

>

> At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

>

> Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

>

> High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

>

> Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

>

> We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

>

> Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

>

> So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

>

> This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

>

> As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

>

> I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

>

> Peace.

> Sue

>

>

> > The future of our children

> > Posted by: "" teamjakob06@... teamjakob06

> > Mon Jul 19, 2010 12:48 pm (PDT)

> >

> >

> >

> > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much.

> >

> > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

> >

> >

>

The New Busy is not the too busy. Combine all your e-mail accounts with Hotmail. Get busy.

Link to comment
Share on other sites

Guest guest

Well put, Robin. That is why it wasn't until six months ago that we realized Liz had aspergers. Before that we thought she was just a bit disorganized and a little different. But then all these school problems popped up and we knew there had to be a reason From: jrisjs@...Date: Tue, 20 Jul 2010 09:20:26 -0700Subject: Re: ( ) Re:The future of our children

I think the problems become more intense when the child gets into homework. Yes, our kids are smart......some may have really high IQ's, but when organization and homework starts to come into play....that's where the crap starts to hit the fan.

We, as parents, couldn't understand why, like you now, our kid is struggling. Having breakdowns,,,,,,,starting to freak out over things that should be so simple. Academics.

The problem for us was when he got a bit older, as many have stated, and socially, they don't fit. Then,,,,when they realize it - it sucks. It can bring out anger and depression and frustrations. You see your kid differently. It crushes you to the core. SEEING that they are different and they they may have to go on a course you honestly didnt' ever see them on because they "were so smart". Hugs to you.

Attack and enjoy every minute of life.

Try everything.....protect everything.

Robin

From: <teamjakob06 >Subject: Re: ( ) Re:The future of our children Date: Tuesday, July 20, 2010, 10:27 AM

I personally am not judging anyone, I am only going on what I have read. Don't get me wrong, we have our good days and bad. I guess what I am struggling to understand and this may very well be because I am not there yet {and hope I never get there}, but what I am not understanding, not all, but some of these children have very high IQ's and are high functioning, like my child, so with that, I cannot see him not having a brighter future and going to college, having a family, etc.. I'm not really worried about the friends thing right now as we seem to have it worked out for now. As far as being offensive to anyone else, this is my opinion only, it is not meant to hurt anyone but it is meant for people to think about the reason they may have been blessed with an Aspie child or children. I also couldn't imagine having more than one Aspie child. Honestly, having one is one thing and having more then one is

another, of course the out come will be different as well as how the child{ren} our raise and how they are involved with their community {church, neighborhood, etc.}. TeamJakobSupport children with Aspergers,With your support their is no limit to Jakob's success!!

From: Comtois <suetoiscox (DOT) net> Sent: Tue, July 20, 2010 9:39:05 AMSubject: ( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare

socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering

why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell

apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program

like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06 teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought

of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a

reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

The New Busy is not the too busy. Combine all your e-mail accounts with Hotmail. Get busy.

Link to comment
Share on other sites

  • 2 weeks later...
Guest guest

You put this so well, Sue. My 20 yo son is considered

gifted with a very high IQ. He was not diagnosed until he was 15. When he

was younger the social issues were not as glaring as they were as he got

older. Trouble with executive functioning, hygiene is a constant

battle, yada, yada, yada. I feel your pain!! A year of community

college – one semester he managed to finish 3 hours and made a B; second

semester finished 6 hours and made an F in both classes and is now on academic

suspension. He does drive and is a very good driver. We have him in

a program called FOPI (Focusing on Personal Independence) and starting the

second year with revised plan and goals. They are going to have him take

an online class, even if it is something with no credits, to see if they can

identify problem areas to target. I have told his dad, whom he lives

with, since he was 17 that he needed to get legal guardianship of him so he can

keep him on his insurance in case he was not successful in college – he is

in the process and I am keeping my fingers crossed that this is done before the

insurance company drops him. I could go on and on.

But, as you said even high functioning kiddos have major hurdles

to overcome and as time goes on we see one dream after another shattered.

From:

[mailto: ] On

Behalf Of Comtois

Sent: Tuesday, July 20, 2010 8:39 AM

Subject: ( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism

of how many of us are raising our children. And I hope you're right.

I hope what you're doing with your son will head off the many problems

that develop as these children get older. We have three sons with AS.

The oldest is 19. The other two are 15 and 12. The 15 yo is

less affected, and will, I think, have a relatively normal future. The 19

yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he

had a bright future ahead of him. There were problems at school but none

of his classmates had really sophisticated social skills and they were very

nonjudgemental. He also had a friend and we had just learned that his

verbal IQ was/is about 200. He taught himself to read grown-up novels

shortly after his third birthday. He was truly brilliant. I was envisioning

a future for him that might include being an author or a college professor.

You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different

state, and we elected to move into a district that had a fabulous program for

gifted kids. The biggest problem for my son was that he eventually lost

contact with that one friend he had (and has never been able to make another

one).

At 8yo he was moved to a full-time gifted program. I

was so proud of him and it just reinforced my hopes for his future. AS

wasn't going to stand in the way of anything for my son. It wasn't going

to be an excuse for a failure to achieve. Yeay! Unfortunately, a

gifted program involves lots of transitions all the time. The typical

gifted children thrived, but my son was totally overwhelmed. The day came

when the principal told us that if we brought him back to school the next day,

he would expel him. I was c! ompletel y new to the IEP world, and didn't

know that this was an empty and illegal threat, so I pulled him out and

homeschooled him for the next couple of years--all the while working on social

skills and learning coping mechanisms. He did *wonderfully* academically,

but when I put him in school I asked them to have his repeat the year we had

just completed to give him an extra year to prepare socially for middle school.

The school agreed, and, again, I was hopeful that things were back on

track for a successful future.

Middle school was a mess. He got lumped in with ED

classes because he needed a smaller group and the same district that has such a

wonderful program for gifted kids has literally nothing for kids with high

functioning autism. The ED kids victimized my son--especially in gym

class--to the point that his teachers had him pulled out of that setting and

moved to an LD setting instead. Well, so much for that brilliant academic

future. LD classes don't move as quickly as even general ed. classes for

obvious reasons.

High school rolled around, and my son got a wonderful case

manager who took a personal interest in him. He was available to support

my son throughout the day, and many of the problems we'd seen in middle school

improved a lot. But he still had no friends, and he was constantly

getting in trouble with his grades because he was so very disorganized.

You see he has executive functioning deficits. Keeping himself as

organized as a typical high school student is literally impossible for him.

Where could he get more help with staying organized? The LD

classes. He did, however, have some non-special ed. classes. Latin

for example--and he did *very* well on tests and quizzes because he has a

photographic memory--but he was still so disorganized about his homework.

Also, by now his lack of friends was really hurting him. He wrote

an entry in his journal co! ncerning how hopeless he felt and wondering why he

didn't just kill himself. I got a call to come to the school immediately.

We talked with his case manager and I took our son home for a mental

health day. We also contacted his psychiatrist (by now he was on several

meds--including ADHD meds in an attempt to improve his executive functioning

skills--so he had a psychiatrist. He was also in social skills therapy

with a social worker, and we brought her in on the problem. The

specialists couldn't really do much about the root of the problem though.

The boy was lonely and you can't *make* other kids accept someone as a

friend. We hoped that he'd make friends with someone from his social skills

group which had several kids with AS, but what we found was that then *neither*

boy had much in the way of social skills, and they would tend to get involved

with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time

to start thinking about what our son would do when he finished high school.

I was still thinking that a 4-year college was a natural choice for such

a smart kid. The case manager gradually broke it to me that our son

should get some trade skills in case college didn't work out. I was

seeing here on this board that *many* parents who tried to send their AS kids

to college were failing despite herculean efforts. Our son's social

worker told me that AS kids " crash and burn " in college. Her

daughter--also with AS--had just completed the required classes for a degree in

teaching, but at the last minute, the faculty informed her that she wouldn't be

granted the degree or certificate or whatever because they knew she lacked the

social skills to teach and they couldn't in good conscience grant her the

credentials she would need to become a teacher. She fell apart (including

moving out and becoming homeless for a while), and her mother was desperately

trying to ! pick up the pieces.

We decided to let our son try the high school's technical

school. Two years later, he has five professional certifications in the

computer repair/website design area. He loves the work, but his

instructors informed me that they don't think he'll be able to hold a job in

the field. Lack of social skills. For example, he finished the unit

way ahead of other kids, but when his teacher asked him to help a fellow

student who was having problems, he wound up asking the kid if he was stupid or

what? Also, that executive functioning issue is rearing it's ugly head

again. He can't really problem solve the way he would need to be able to

in a professional capacity.

Then there are the day to day issues. He can't

remember to take his medicine by himself. Simple problems confuse him because

he has trouble generalizing one experience to a similar, but different, one in

the future. Personal hygiene is getting better, but we still have to

remind him every day to use deodorant, shave, and brush his teeth. If we

don't do that, it doesn't get done because he really can't see why he should

care about how other people see him.

So here we are. He's 19 and taking a fifth year of

high school to give him a little more developmental time (kids with IEPs can do

that). His psychiatrist suggested that we needed to make him our ward

because he still needs someone to take care of him--we're hoping he'll

" grow out of " this, but realistically, only time will tell whether

that's possible. I've had him evaluated by the Department of Rehabilitative

Services, so he can get job placement and job coaching help--but I'm worried

that means they'll get him hired on at Mc's to sweep the floor. I

*still* want to see him go to college, but we've learned that colleges that

offer support programs for kids with AS are *very* expensive. There's a

really attractive program ! at NYIT- -but it's so expensive that we can't

possibly afford it. I'm supposed to be working on getting our son

qualified for SSI because we could use that income to help him with a program like

that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost

you, because what I really want to say is that even *very* high functioning

children (and their parents) have major hurdles to overcome. The social

and executive function deficits are *so* much more handicapping than you think

they are when your child is very young. Also, children who can be

diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most

kids who are truly high functioning Aspies aren't diagnosable until they're in

late grade school or even high school because they can compensate up until

then.

As a parent, raising a child with Asperger's can mean

dealing with the death of one dream after another for your child's future.

It truly is heartbreaking. I know because we're living it. My

son is still a wonderful person. He's sweet and innocent in a way that

other people aren't. He's cute. He's brilliant. And yet none

of that is enough to keep him from having the sort of limited future I could

never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a

different pathway from ours. It's entirely possible that it will because

every person with AS is different from every other person with AS. I'm

just saying you need to be careful about judging other parents because you

could so easily be walking in their shoes in ten years.

Peace.

Sue

The

future of our children

Posted by:

" " teamjakob06@... teamjakob06

Mon Jul 19, 2010

12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about

my child's future. I have NO doubt in my mind that my son will be a productive,

sucessful citizen. I homeschool him and we get very indepth with certain

subjects. He can learn much better than at a private or public school and the

resources are endless. He is 7 now and when he graduates he will attend college

like every other child in America. It will not be a special college either, it

may very well be Washington University as it is in our city of

Fredericksburg. I know that one day he too will have a family and I look

forward to having grandchildren. Not one time have I ever thought that he would

be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa,

etc.. Not one time have I thought that he would never amount to much or ever

let him think that. Never ever have I thought of his disability as a bad thing.

There is greatness in all these children and our job is to guide them to become

greatness! Sometimes I think that we tend to hinder our children more than

their disability by setting the bar so low that they believe thenselves that

they can't do anything or won't amount to much.

We used to live in Georgia and they had very li! ttle res ources to help, so I

moved to Virginia, where I was born and my parents were raised. Here there is a

lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP

YOU GET IT! You have to do your home work as I have read that many of you have

and you have to know, have to have faith, and have to believe that God blessed

you with this special child for a reason! The road is less traveled, tiring,

and we all feel that we are treading on broken glass barefoot, but we all

choose to be parents even though God choose us to be parents of Aspie children,

again for a reason! If you stop clipping their wings and allow them to fly, who

knows how high they will soar!

Link to comment
Share on other sites

Guest guest

depending on your insurance... a letter from your psychatrist / doctor stating your son's disabilities will allow him to stay on your insurance.

\ RE: ( ) Re:The future of our children

You put this so well, Sue. My 20 yo son is considered gifted with a very high IQ. He was not diagnosed until he was 15. When he was younger the social issues were not as glaring as they were as he got older. Trouble with executive functioning, hygiene is a constant battle, yada, yada, yada. I feel your pain!! A year of community college – one semester he managed to finish 3 hours and made a B; second semester finished 6 hours and made an F in both classes and is now on academic suspension. He does drive and is a very good driver. We have him in a program called FOPI (Focusing on Personal Independence) and starting the second year with revised plan and goals. They are going to have him take an online class, even if it is something with no credits, to see if they can identify problem areas to target. I have told his dad, whom he lives with, since he was 17 that he needed to get legal guardianship of him so he can keep him on his insurance in case he was not successful in college – he is in the process and I am keeping my fingers crossed that this is done before the insurance company drops him. I could go on and on.

But, as you said even high functioning kiddos have major hurdles to overcome and as time goes on we see one dream after another shattered.

From: [mailto: ] On Behalf Of ComtoisSent: Tuesday, July 20, 2010 8:39 AM Subject: ( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was c! ompletel y new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal co! ncerning how hopeless he felt and wondering why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell apart (including moving out and becoming homeless for a while), and her mother was desperately trying to ! pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program ! at NYIT- -but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06@... teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much. We used to live in Georgia and they had very li! ttle res ources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

Link to comment
Share on other sites

Guest guest

People

are getting angry because of the way you are wording your thoughts. This is one of many posts in a row just like this. From what you write, I

am getting the idea that you believe our kids are struggling because we

are just incompetent or not trying hard enough or do not have enough faith. I'm sure this is a comfort to feel better about yourself by putting others down. But it hardly seems you should be surprised at how other people would take being put down like this. And to believe that only you have discovered the cure after centuries of parents before

you, I don't understand that thinking process. It is just not realistic. But more importantly, it is not supportive to anyone in our community. And that is the part that really ticks me off with this thread. As if we all just wish to have the problems we are facing, are too lazy or as in a previous post, we just don't "aim high enough." That is complete nonsense and not true. But again, it is so unsupportive of people's real problems that I think it's mean to say that. it's one thing to secretly believe you are immune and have all the answers but another to say that on a regular basis, stomping on people's feelings the whole way. And then you say you are sorry it hurt

feelings but not sorry for what you said? I do not even understand how

you could separate those two things from each other. My former sped director used to have a saying for moments like this, "They don't know what they don't know."

Being a good parent is nice, but it does not prevent kids with AS/HFA from struggling to achieve even basic skills. Believing in God is a good thing (and I do, having been raised by a minister) but that does not protect you from the effects the disability of autism has on your child. (if anything, it should make you more aware and tolerant, not less so.) Having a high IQ is nice, a perk in the otherwise problematic

scheme of the disability. But what good is it really? It's mighty handy if you are going to be taking an IQ test for a living or your friends or boss will choose you as a friend or employee just because you

scored high on an IQ test. Somehow, though, I don't think the world works that way. And I don't recall the last time someone asked me my grades from high school. Life sorta didn't care after that. Nor did having an "A" in Geometry in high school mean I was immune to having kids with autism, learning disabilities or that I magically knew all the

answers to make these problems disappear either when I became a mother. And how you could believe that wishing the problems away would actually make them go away? I don't understand this concept. Maybe I am just not bright enough. But it makes zero sense to me.

In this post, you just wrote, "I will not allow him to sit alone in his room scared of the world" as if there are other parents here who do that. It is extremely insulting for you to say such a thing, as if we are all doing just that. You think your own force of will will make these problems disappear or not happen. Someone said they hoped you were right but I will go farther and say you are so wrong. I think it's

a childish notion to believe life works that way. Wouldn't it be nice if life worked like that?

And frankly, the people I have talked to for all these many years on this list are some of the most resilient people I have ever met. They don't give up, they aim really high and they work twice as hard as other

parents to achieve even parts of the same thing. They are inspiring and hopeful and also realistic. They get up and do what needs doing, even when it would be easier to run and hide. I feel insulted not only for myself, but for all the people on this list who work so hard for so little and nobody should make any of us feel as if we just need to try harder, aim higher or stop "letting" our kids have these problems. You just have no clue. I can't even express this in words. I just feel so angry right now to be judged by someone who has no clue what I've been through and then on behalf of these wonderful people that I have met along the way. I have seen them struggle and cry and push and work past

the point of reason. Lesser people would have run long ago. But we show up every day, rain or shine. Kudos to us! I feel like this is a slap in the face to them to even insinuate that they just need to try harder and they would not have these problems. I can't even continue because it just makes me want to say, "ARGH!"

I thought then that you must just post to see if anyone will argue. Some people do that, so maybe that is the goal? Stir things up? I can't fathom another parent not even understanding this or making these kinds of assumptions about other people like this. We get that from neighbors, teachers, administrators. But other parents who have kids with autism/AS? I am really unable to understand this. So these posts are done. If I want to listen to people say ignorant things about my kids, I would go back to the school and let them lecture me or better yet, grab a few of my pompous neighbors who think having a disability is

a punishment for being bad. I mean, this is just such a ridiculous thread. I thought it would be just one or two posts at most. But it just lives on. And as for not being sorry for what you said. I just can't think of how to say what I think without sounding extremely rude.

This whole concept is rude and mean spirited. So I will apologize for your posts and I am sorry I did not catch this thread sooner and shut it

off immediately.

Roxanna

Whenever I feel blue, I start breathing again.

( ) Re:The future of our children

Thank you. Thank you. Thank you. You expressed beautifully what I was too upset and angry to say, I am glad you did not cut a single word.

Sue in TN

>

> I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

>

> When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead

of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

>

> When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

>

> At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't

going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

>

> Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the

same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

>

> High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying

organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped

that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

>

> Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty

informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

>

> We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't

really problem solve the way he would need to be able to in a professional capacity.

>

> Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

>

> So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the

Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

>

> This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also,

children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

>

> As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

>

> I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be

careful about judging other parents because you could so easily be walking in their shoes in ten years.

>

> Peace.

> Sue

>

>

> > The future of our children

> > Posted by: "" teamjakob06@... teamjakob06

> > Mon Jul 19, 2010 12:48 pm (PDT)

> >

> >

> >

> > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I

look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much.

> >

> > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have

to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

> >

> >

>

Link to comment
Share on other sites

Guest guest

Amen Roxanne. I know I have lived a life tired of people telling me that I should just give my daughter a licking and her attitude would improve. Time wears one down with this one. From: Roxanna <MadIdeas@...> Sent: Wed, August 4, 2010 12:13:45 PMSubject: Re: ( ) Re:The future of our children

People

are getting angry because of the way you are wording your thoughts. This is one of many posts in a row just like this. From what you write, I

am getting the idea that you believe our kids are struggling because we

are just incompetent or not trying hard enough or do not have enough faith. I'm sure this is a comfort to feel better about yourself by putting others down. But it hardly seems you should be surprised at how other people would take being put down like this. And to believe that only you have discovered the cure after centuries of parents before

you, I don't understand that thinking process. It is just not realistic. But more importantly, it is not supportive to anyone in our community. And that is the part that really ticks me off with this thread. As if we all just wish to have the problems we are facing, are too lazy or as in a previous post, we just don't "aim high enough." That is complete nonsense and not true. But again, it is so unsupportive of people's real problems that I think it's mean to say that. it's one thing to secretly believe you are immune and have all the answers but another to say that on a regular basis, stomping on people's feelings the whole way. And then you say you are sorry it hurt

feelings but not sorry for what you said? I do not even understand how

you could separate those two things from each other. My former sped director used to have a saying for moments like this, "They don't know what they don't know."

Being a good parent is nice, but it does not prevent kids with AS/HFA from struggling to achieve even basic skills. Believing in God is a good thing (and I do, having been raised by a minister) but that does not protect you from the effects the disability of autism has on your child. (if anything, it should make you more aware and tolerant, not less so.) Having a high IQ is nice, a perk in the otherwise problematic

scheme of the disability. But what good is it really? It's mighty handy if you are going to be taking an IQ test for a living or your friends or boss will choose you as a friend or employee just because you

scored high on an IQ test. Somehow, though, I don't think the world works that way. And I don't recall the last time someone asked me my grades from high school. Life sorta didn't care after that. Nor did having an "A" in Geometry in high school mean I was immune to having kids with autism, learning disabilities or that I magically knew all the

answers to make these problems disappear either when I became a mother. And how you could believe that wishing the problems away would actually make them go away? I don't understand this concept. Maybe I am just not bright enough. But it makes zero sense to me.

In this post, you just wrote, "I will not allow him to sit alone in his room scared of the world" as if there are other parents here who do that. It is extremely insulting for you to say such a thing, as if we are all doing just that. You think your own force of will will make these problems disappear or not happen. Someone said they hoped you were right but I will go farther and say you are so wrong. I think it's

a childish notion to believe life works that way. Wouldn't it be nice if life worked like that?

And frankly, the people I have talked to for all these many years on this list are some of the most resilient people I have ever met. They don't give up, they aim really high and they work twice as hard as other

parents to achieve even parts of the same thing. They are inspiring and hopeful and also realistic. They get up and do what needs doing, even when it would be easier to run and hide. I feel insulted not only for myself, but for all the people on this list who work so hard for so little and nobody should make any of us feel as if we just need to try harder, aim higher or stop "letting" our kids have these problems. You just have no clue. I can't even express this in words. I just feel so angry right now to be judged by someone who has no clue what I've been through and then on behalf of these wonderful people that I have met along the way. I have seen them struggle and cry and push and work past

the point of reason. Lesser people would have run long ago. But we show up every day, rain or shine. Kudos to us! I feel like this is a slap in the face to them to even insinuate that they just need to try harder and they would not have these problems. I can't even continue because it just makes me want to say, "ARGH!"

I thought then that you must just post to see if anyone will argue. Some people do that, so maybe that is the goal? Stir things up? I can't fathom another parent not even understanding this or making these kinds of assumptions about other people like this. We get that from neighbors, teachers, administrators. But other parents who have kids with autism/AS? I am really unable to understand this. So these posts are done. If I want to listen to people say ignorant things about my kids, I would go back to the school and let them lecture me or better yet, grab a few of my pompous neighbors who think having a disability is

a punishment for being bad. I mean, this is just such a ridiculous thread. I thought it would be just one or two posts at most. But it just lives on. And as for not being sorry for what you said. I just can't think of how to say what I think without sounding extremely rude.

This whole concept is rude and mean spirited. So I will apologize for your posts and I am sorry I did not catch this thread sooner and shut it

off immediately.

Roxanna

Whenever I feel blue, I start breathing again.

( ) Re:The future of our children

Thank you. Thank you. Thank you. You expressed beautifully what I was too upset and angry to say, I am glad you did not cut a single word.

Sue in TN

>

> I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

>

> When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead

of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

>

> When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

>

> At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't

going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

>

> Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the

same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

>

> High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying

organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped

that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

>

> Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty

informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

>

> We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't

really problem solve the way he would need to be able to in a professional capacity.

>

> Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

>

> So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the

Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

>

> This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also,

children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

>

> As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

>

> I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be

careful about judging other parents because you could so easily be walking in their shoes in ten years.

>

> Peace.

> Sue

>

>

> > The future of our children

> > Posted by: "" teamjakob06@ ... teamjakob06

> > Mon Jul 19, 2010 12:48 pm (PDT)

> >

> >

> >

> > Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I

look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much.

> >

> > We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have

to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

> >

> >

>

Link to comment
Share on other sites

Guest guest

Wow, how crappy to have that old lady judging you and the kids each week. I wouldn't have lasted.

Roxanna

Whenever I feel blue, I start breathing again.

Re: ( ) Re:The future of our children



As far as church goes. I am with Robin.. I have never felt so unaccepted as when I attempted church with my kids. With my son's age group there was a little old lady who gave out candy to all the "good " kids after Sunday School . Of course, she always left my kids out since they were not "good" (meaning quiet). When I tried again with my granddaughter, it went ok until the day they introduced loud music to the program, and she wouldn't participate and, again, the little old lady that was the class "shepherd" screamed across the whole Sunday School gathering that "That girl needs therapy!" and later explained that she was only trying to let us know that she is in deep need of help. She harrassed several other kids, too, but my husband would no longer attend church, nor my daughter and I have quit trying too. I talk to God at home.

( ) Re:The future of our children

I hope I'm wrong, but I read you post as a kind of criticism of how many of us are raising our children. And I hope you're right. I hope what you're doing with your son will head off the many problems that develop as these children get older. We have three sons with AS. The oldest is 19. The other two are 15 and 12. The 15 yo is less affected, and will, I think, have a relatively normal future. The 19 yo and the 12 yo are facing a different set of challenges.

When my 19yo was 7 the way your son is now, I too thought he had a bright future ahead of him. There were problems at school but none of his classmates had really sophisticated social skills and they were very nonjudgemental. He also had a friend and we had just learned that his verbal IQ was/is about 200. He taught himself to read grown-up novels shortly after his third birthday. He was truly brilliant. I was envisioning a future for him that might include being an author or a college professor. You know, quirky, but brilliant.

When he was 7 1/2 the military transferred us to a different state, and we elected to move into a district that had a fabulous program for gifted kids. The biggest problem for my son was that he eventually lost contact with that one friend he had (and has never been able to make another one).

At 8yo he was moved to a full-time gifted program. I was so proud of him and it just reinforced my hopes for his future. AS wasn't going to stand in the way of anything for my son. It wasn't going to be an excuse for a failure to achieve. Yeay! Unfortunately, a gifted program involves lots of transitions all the time. The typical gifted children thrived, but my son was totally overwhelmed. The day came when the principal told us that if we brought him back to school the next day, he would expel him. I was completely new to the IEP world, and didn't know that this was an empty and illegal threat, so I pulled him out and homeschooled him for the next couple of years--all the while working on social skills and learning coping mechanisms. He did *wonderfully* academically, but when I put him in school I asked them to have his repeat the year we had just completed to give him an extra year to prepare socially for middle school. The school agreed, and, again, I was hopeful that things were back on track for a successful future.

Middle school was a mess. He got lumped in with ED classes because he needed a smaller group and the same district that has such a wonderful program for gifted kids has literally nothing for kids with high functioning autism. The ED kids victimized my son--especially in gym class--to the point that his teachers had him pulled out of that setting and moved to an LD setting instead. Well, so much for that brilliant academic future. LD classes don't move as quickly as even general ed. classes for obvious reasons.

High school rolled around, and my son got a wonderful case manager who took a personal interest in him. He was available to support my son throughout the day, and many of the problems we'd seen in middle school improved a lot. But he still had no friends, and he was constantly getting in trouble with his grades because he was so very disorganized. You see he has executive functioning deficits. Keeping himself as organized as a typical high school student is literally impossible for him. Where could he get more help with staying organized? The LD classes. He did, however, have some non-special ed. classes. Latin for example--and he did *very* well on tests and quizzes because he has a photographic memory--but he was still so disorganized about his homework. Also, by now his lack of friends was really hurting him. He wrote an entry in his journal concerning how hopeless he felt and wondering why he didn't just kill himself. I got a call to come to the school immediately. We talked with his case manager and I took our son home for a mental health day. We also contacted his psychiatrist (by now he was on several meds--including ADHD meds in an attempt to improve his executive functioning skills--so he had a psychiatrist. He was also in social skills therapy with a social worker, and we brought her in on the problem. The specialists couldn't really do much about the root of the problem though. The boy was lonely and you can't *make* other kids accept someone as a friend. We hoped that he'd make friends with someone from his social skills group which had several kids with AS, but what we found was that then *neither* boy had much in the way of social skills, and they would tend to get involved with their focal interests and ignore each other.

Skipping forward a couple of years, we found that it was time to start thinking about what our son would do when he finished high school. I was still thinking that a 4-year college was a natural choice for such a smart kid. The case manager gradually broke it to me that our son should get some trade skills in case college didn't work out. I was seeing here on this board that *many* parents who tried to send their AS kids to college were failing despite herculean efforts. Our son's social worker told me that AS kids "crash and burn" in college. Her daughter--also with AS--had just completed the required classes for a degree in teaching, but at the last minute, the faculty informed her that she wouldn't be granted the degree or certificate or whatever because they knew she lacked the social skills to teach and they couldn't in good conscience grant her the credentials she would need to become a teacher. She fell apart (including moving out and becoming homeless for a while), and her mother was desperately trying to pick up the pieces.

We decided to let our son try the high school's technical school. Two years later, he has five professional certifications in the computer repair/website design area. He loves the work, but his instructors informed me that they don't think he'll be able to hold a job in the field. Lack of social skills. For example, he finished the unit way ahead of other kids, but when his teacher asked him to help a fellow student who was having problems, he wound up asking the kid if he was stupid or what? Also, that executive functioning issue is rearing it's ugly head again. He can't really problem solve the way he would need to be able to in a professional capacity.

Then there are the day to day issues. He can't remember to take his medicine by himself. Simple problems confuse him because he has trouble generalizing one experience to a similar, but different, one in the future. Personal hygiene is getting better, but we still have to remind him every day to use deodorant, shave, and brush his teeth. If we don't do that, it doesn't get done because he really can't see why he should care about how other people see him.

So here we are. He's 19 and taking a fifth year of high school to give him a little more developmental time (kids with IEPs can do that). His psychiatrist suggested that we needed to make him our ward because he still needs someone to take care of him--we're hoping he'll "grow out of" this, but realistically, only time will tell whether that's possible. I've had him evaluated by the Department of Rehabilitative Services, so he can get job placement and job coaching help--but I'm worried that means they'll get him hired on at Mc's to sweep the floor. I *still* want to see him go to college, but we've learned that colleges that offer support programs for kids with AS are *very* expensive. There's a really attractive program at NYIT--but it's so expensive that we can't possibly afford it. I'm supposed to be working on getting our son qualified for SSI because we could use that income to help him with a program like that, but I'm kind of overwhelmed and *he* certainly can't do it himself.

This has gotten hideously long, and I hope I haven't lost you, because what I really want to say is that even *very* high functioning children (and their parents) have major hurdles to overcome. The social and executive function deficits are *so* much more handicapping than you think they are when your child is very young. Also, children who can be diagnosed at 5 or 6 yo probably *aren't* all that high functioning. Most kids who are truly high functioning Aspies aren't diagnosable until they're in late grade school or even high school because they can compensate up until then.

As a parent, raising a child with Asperger's can mean dealing with the death of one dream after another for your child's future. It truly is heartbreaking. I know because we're living it. My son is still a wonderful person. He's sweet and innocent in a way that other people aren't. He's cute. He's brilliant. And yet none of that is enough to keep him from having the sort of limited future I could never have envisioned for him when he was 7yo.

I sincerely hope that your experience with AS follows a different pathway from ours. It's entirely possible that it will because every person with AS is different from every other person with AS. I'm just saying you need to be careful about judging other parents because you could so easily be walking in their shoes in ten years.

Peace.

Sue

The future of our children

Posted by: "" teamjakob06 teamjakob06

Mon Jul 19, 2010 12:48 pm (PDT)

Lately I have been reading some of the posts on here and thinking a lot about my child's future. I have NO doubt in my mind that my son will be a productive, sucessful citizen. I homeschool him and we get very indepth with certain subjects. He can learn much better than at a private or public school and the resources are endless. He is 7 now and when he graduates he will attend college like every other child in America. It will not be a special college either, it may very well be Washington University as it is in our city of Fredericksburg. I know that one day he too will have a family and I look forward to having grandchildren. Not one time have I ever thought that he would be a stock boy at Walmart or the service guy at our local Exxon, Shell, Wawa, etc.. Not one time have I thought that he would never amount to much or ever let him think that. Never ever have I thought of his disability as a bad thing. There is greatness in all these children and our job is to guide them to become greatness! Sometimes I think that we tend to hinder our children more than their disability by setting the bar so low that they believe thenselves that they can't do anything or won't amount to much.

We used to live in Georgia and they had very little resources to help, so I moved to Virginia, where I was born and my parents were raised. Here there is a lot of help, BUT DON'T RELY ON THE SCHOOL SYSTEM TO TELL YOU ABOUT IT OR HELP YOU GET IT! You have to do your home work as I have read that many of you have and you have to know, have to have faith, and have to believe that God blessed you with this special child for a reason! The road is less traveled, tiring, and we all feel that we are treading on broken glass barefoot, but we all choose to be parents even though God choose us to be parents of Aspie children, again for a reason! If you stop clipping their wings and allow them to fly, who knows how high they will soar!

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...