Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 That is very kind of you to say. I remember the social worker saying that I had done a good job with n and it made me feel really good. Perhaps they just say that to everyone ... I'm sure they know we are all basket cases of uncertainty. Thanks, (SAHM in GA) MSN elizabethloht@... n 33, mo, no formal dx Phoebe, 12 weeks Re: The cotinuing march toward diagnosis > > > > > This morning I packed up the kids for an " in-take " interview with the > developmental pediatrician. I spent the night before reviewing n's > medical history and various evaluations, trying to correct the inaccuracies. > > As many of you may be able to relate, I was terrified at the prospect of > managing both kids in an unfamiliar environment by myself. Should I put > n in the stroller and carry Phoebe? Put Phoebe in the car sear carrier > and n in the stroller? Can I carry all that? Can I possibly manage > n out of a stroller? > > Well the office had steps out front so I knew I would have to forego the > stroller. This made me quite nervous. But I took n by the hand, > lugging Phoebe in her carrier, determined to make the best of it. We were > early ... > > Once inside n began to help himself to office supplies at the front > desk and pushing buttons on the copier. The front desk attendant did not > seem thrilled. Things did not bode well. We were directed to a waiting > room in the back. Thankfully n followed. I was given a clipboard of > paperwork. I laughed to myself thinking it would be impossible to fill it > out with n on the loose. However n found a tupperware container > of matchbox cars and began to happily obsess on them, which was convenient. > > The social worker then directed us into a back office, n followed of > his own accord, which was down right shocking. Inside he located a box of > crayons, colored pencils, and markers. He happily proceeded to line them up > and tote them about. Phoebe dozed in her carrier. Again, convenient so I > could take to the social worker. > > She was a very nice lady who was very kind to n. We spoke of n's > history, his many evaluations, therapies, etc, touching briefly here and > there on my personally journey in coming to terms with his challenges. Yes, > I told her, I think he is autistic, that's why we're here. In the past I > had made every imaginable excuse to explain away his " quirks " . And, yes, it > makes me feel like a bad *evil* mother to say that I am no longer holding > out hope that he will " just be a late bloomer " or " grow out of it " . I need > answers as we approach the school dilemma. > > She felt fairly certain based on what I had told her and what she observed > that we would get a spectrum diagnosis. I was surprised at how easily t his > she made this determination. I like to think that n's autistic > tendencies are subtle ... But then our ST said the same thing within the > first two visits. > > She recommended that we begin the process for n to be evaluated by the > school district for special ed preschool. However I am somewhat ashamed to > admit that I am reluctant to do this. Naturally I want n to have as > many therapies as we can get, but a part of me balks at the finality of > enrolling him in special ed preschool. I know it will be a lightening rod > issue in our family, that extended members will openly question my judgment, > try to call and talk me out of it. And even I must concede that I second > guess myself daily. > > Did I feel emotionally crushed when the social worker said she did indeed > think he was on the spectrum? No. I had expected it. But on the way home > I began thinking about how much n is the center of our lives and that > we just adore him. And how he was such a wonderful baby. He was so good, > you could take him anywhere. And I thought about how profoundly grateful I > was for that first year when he was just my perfect little baby. Then I had > some tears. > > This is tough. > > (SAHM in GA) > MSN elizabethloht@... > n 33, mo, no formal > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 Yes, I don't know how I'm going to handle this either. I mean, around the holidays, do you send out the usual cards with little letters casually mentioning that your child was dx as autistic? Is that weird? (SAHM in GA) MSN elizabethloht@... n 33, mo, no formal dx Phoebe, 12 weeks Re: The cotinuing march toward diagnosis > > > > > > > > > > This morning I packed up the kids for an " in-take " interview with the > > developmental pediatrician. I spent the night before reviewing n's > > medical history and various evaluations, trying to correct the > inaccuracies. > > > > As many of you may be able to relate, I was terrified at the prospect of > > managing both kids in an unfamiliar environment by myself. Should I put > > n in the stroller and carry Phoebe? Put Phoebe in the car sear > carrier > > and n in the stroller? Can I carry all that? Can I possibly > manage > > n out of a stroller? > > > > Well the office had steps out front so I knew I would have to forego the > > stroller. This made me quite nervous. But I took n by the hand, > > lugging Phoebe in her carrier, determined to make the best of it. We > were > > early ... > > > > Once inside n began to help himself to office supplies at the front > > desk and pushing buttons on the copier. The front desk attendant did > not > > seem thrilled. Things did not bode well. We were directed to a waiting > > room in the back. Thankfully n followed. I was given a clipboard > of > > paperwork. I laughed to myself thinking it would be impossible to fill > it > > out with n on the loose. However n found a tupperware > container > > of matchbox cars and began to happily obsess on them, which was > convenient. > > > > The social worker then directed us into a back office, n followed > of > > his own accord, which was down right shocking. Inside he located a box > of > > crayons, colored pencils, and markers. He happily proceeded to line > them up > > and tote them about. Phoebe dozed in her carrier. Again, convenient so > I > > could take to the social worker. > > > > She was a very nice lady who was very kind to n. We spoke of > n's > > history, his many evaluations, therapies, etc, touching briefly here and > > there on my personally journey in coming to terms with his challenges. > Yes, > > I told her, I think he is autistic, that's why we're here. In the past > I > > had made every imaginable excuse to explain away his " quirks " . And, > yes, it > > makes me feel like a bad *evil* mother to say that I am no longer > holding > > out hope that he will " just be a late bloomer " or " grow out of it " . I > need > > answers as we approach the school dilemma. > > > > She felt fairly certain based on what I had told her and what she > observed > > that we would get a spectrum diagnosis. I was surprised at how easily > this > > she made this determination. I like to think that n's autistic > > tendencies are subtle ... But then our ST said the same thing within > the > > first two visits. > > > > She recommended that we begin the process for n to be evaluated by > the > > school district for special ed preschool. However I am somewhat ashamed > to > > admit that I am reluctant to do this. Naturally I want n to have > as > > many therapies as we can get, but a part of me balks at the finality of > > enrolling him in special ed preschool. I know it will be a lightening > rod > > issue in our family, that extended members will openly question my > judgment, > > try to call and talk me out of it. And even I must concede that I > second > > guess myself daily. > > > > Did I feel emotionally crushed when the social worker said she did > indeed > > think he was on the spectrum? No. I had expected it. But on the way > home > > I began thinking about how much n is the center of our lives and > that > > we just adore him. And how he was such a wonderful baby. He was so > good, > > you could take him anywhere. And I thought about how profoundly > grateful I > > was for that first year when he was just my perfect little baby. Then I > had > > some tears. > > > > This is tough. > > > > (SAHM in GA) > > MSN elizabethloht@... > > n 33, mo, no formal > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 Yes, I don't know how I'm going to handle this either. I mean, around the holidays, do you send out the usual cards with little letters casually mentioning that your child was dx as autistic? Is that weird? (SAHM in GA) MSN elizabethloht@... n 33, mo, no formal dx Phoebe, 12 weeks Re: The cotinuing march toward diagnosis > > > > > > > > > > This morning I packed up the kids for an " in-take " interview with the > > developmental pediatrician. I spent the night before reviewing n's > > medical history and various evaluations, trying to correct the > inaccuracies. > > > > As many of you may be able to relate, I was terrified at the prospect of > > managing both kids in an unfamiliar environment by myself. Should I put > > n in the stroller and carry Phoebe? Put Phoebe in the car sear > carrier > > and n in the stroller? Can I carry all that? Can I possibly > manage > > n out of a stroller? > > > > Well the office had steps out front so I knew I would have to forego the > > stroller. This made me quite nervous. But I took n by the hand, > > lugging Phoebe in her carrier, determined to make the best of it. We > were > > early ... > > > > Once inside n began to help himself to office supplies at the front > > desk and pushing buttons on the copier. The front desk attendant did > not > > seem thrilled. Things did not bode well. We were directed to a waiting > > room in the back. Thankfully n followed. I was given a clipboard > of > > paperwork. I laughed to myself thinking it would be impossible to fill > it > > out with n on the loose. However n found a tupperware > container > > of matchbox cars and began to happily obsess on them, which was > convenient. > > > > The social worker then directed us into a back office, n followed > of > > his own accord, which was down right shocking. Inside he located a box > of > > crayons, colored pencils, and markers. He happily proceeded to line > them up > > and tote them about. Phoebe dozed in her carrier. Again, convenient so > I > > could take to the social worker. > > > > She was a very nice lady who was very kind to n. We spoke of > n's > > history, his many evaluations, therapies, etc, touching briefly here and > > there on my personally journey in coming to terms with his challenges. > Yes, > > I told her, I think he is autistic, that's why we're here. In the past > I > > had made every imaginable excuse to explain away his " quirks " . And, > yes, it > > makes me feel like a bad *evil* mother to say that I am no longer > holding > > out hope that he will " just be a late bloomer " or " grow out of it " . I > need > > answers as we approach the school dilemma. > > > > She felt fairly certain based on what I had told her and what she > observed > > that we would get a spectrum diagnosis. I was surprised at how easily > this > > she made this determination. I like to think that n's autistic > > tendencies are subtle ... But then our ST said the same thing within > the > > first two visits. > > > > She recommended that we begin the process for n to be evaluated by > the > > school district for special ed preschool. However I am somewhat ashamed > to > > admit that I am reluctant to do this. Naturally I want n to have > as > > many therapies as we can get, but a part of me balks at the finality of > > enrolling him in special ed preschool. I know it will be a lightening > rod > > issue in our family, that extended members will openly question my > judgment, > > try to call and talk me out of it. And even I must concede that I > second > > guess myself daily. > > > > Did I feel emotionally crushed when the social worker said she did > indeed > > think he was on the spectrum? No. I had expected it. But on the way > home > > I began thinking about how much n is the center of our lives and > that > > we just adore him. And how he was such a wonderful baby. He was so > good, > > you could take him anywhere. And I thought about how profoundly > grateful I > > was for that first year when he was just my perfect little baby. Then I > had > > some tears. > > > > This is tough. > > > > (SAHM in GA) > > MSN elizabethloht@... > > n 33, mo, no formal > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 Thanks, . I know you're right. It just seems like every week I hear a " short bus " joke somewhere, and that makes special education seem like such a stigma. I guess I'm going to have to toughen up about it : ) (SAHM in GA) MSN elizabethloht@... n 33, mo, no formal dx Phoebe, 12 weeks Re: The cotinuing march toward diagnosis > Sweetie - > > If he goes into a special education class it does not by any means classify > him as anything other than what he is now - a child with challenges. I > always thought was subtle too. Now that I see her with typical > children it's as obvious as an a red light. (But remember she only needed > the special ed class for 6 months). When you're home you are comparing him to > himself before any services. When you're in school you're comparing him to > the other children. That's how he will make progress - by determining where > he needs the extra help weather it's turntaking, pragmatic langauge or > pretend play. > > Extra services will not hurt him as long as he's in the proper placement for > HIM. My best friend's son has been with services for 2 1/2 years and she is > just now coming to terms with the diagnois. You don't have to send out a > card that says My Son is in Special Education - you don't even have to tell > anyone. That's a personal choice. I'm sorry that your family is not being > supportive... mine isn't really either and it sucks. > > Hugs > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 Thanks, . I know you're right. It just seems like every week I hear a " short bus " joke somewhere, and that makes special education seem like such a stigma. I guess I'm going to have to toughen up about it : ) (SAHM in GA) MSN elizabethloht@... n 33, mo, no formal dx Phoebe, 12 weeks Re: The cotinuing march toward diagnosis > Sweetie - > > If he goes into a special education class it does not by any means classify > him as anything other than what he is now - a child with challenges. I > always thought was subtle too. Now that I see her with typical > children it's as obvious as an a red light. (But remember she only needed > the special ed class for 6 months). When you're home you are comparing him to > himself before any services. When you're in school you're comparing him to > the other children. That's how he will make progress - by determining where > he needs the extra help weather it's turntaking, pragmatic langauge or > pretend play. > > Extra services will not hurt him as long as he's in the proper placement for > HIM. My best friend's son has been with services for 2 1/2 years and she is > just now coming to terms with the diagnois. You don't have to send out a > card that says My Son is in Special Education - you don't even have to tell > anyone. That's a personal choice. I'm sorry that your family is not being > supportive... mine isn't really either and it sucks. > > Hugs > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 Jacquie, thank you for saying so. (SAHM in GA) MSN elizabethloht@... n 33, mo, no formal dx Phoebe, 12 weeks Re: The cotinuing march toward diagnosis > > Oh, , I believe a bad evil mother would be one who never faced the > reality that something needed to be addressed and just denied everything -- > because that would do n so much more harm than good. > > You are a good mother for recognizing the truths and searching out the ways > to deal with them so that n can grow and progress and fulfill all of > his potential as soon as he can. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 Jacquie, thank you for saying so. (SAHM in GA) MSN elizabethloht@... n 33, mo, no formal dx Phoebe, 12 weeks Re: The cotinuing march toward diagnosis > > Oh, , I believe a bad evil mother would be one who never faced the > reality that something needed to be addressed and just denied everything -- > because that would do n so much more harm than good. > > You are a good mother for recognizing the truths and searching out the ways > to deal with them so that n can grow and progress and fulfill all of > his potential as soon as he can. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 The short bus. LOL! Sorry. Where and I grew up the short bus was a joke. I mean, they were supposed to be the sped kids but where we were sped ment the kids that no one wanted to deal with. You know, the problem cases, not necessary the sped cases. The kids that had an attitude about school and were failing because they didn't do their work and they dumped them in, what we always refered to as " the retarded class " . Now, the one school that I went to sped was just that sped. The kids with various learning problems were in there, not the ones that didn't want to be in school and do work. And they didn't ride the " short bus " . We didn't have a short bus for that district. The sped was right in the school, the classroom was on the bottom floor down from the caffateria (there weren't any other classrooms down there but the gym, the TAG room and the art room. The kids in sped stayed in that room from K through 6 and the teacher in there was great with them. There were one or two kids that weren't in sped that should have been but they did just fine in regular classes. ended up in sped adventually. When we moved up to the jr high there was a sped room there was well that these kids spent most of their time in. on the other hand.... I feel so bad about how he was treated now knowing what I know now about autism. was a really tall and big kid even in 6th grade. In 7th he was like 6 feet tall. The one thing that I picked on him about was the green pepper strips that he had to have in his lunch every day. Did not understand how anyone could eat them (then again, at the time they gave me heartburn. LOL). Anyway, he was this huge kid and had the emotional materity of a kindergartner. He was really easy for people to pick on. I didn't really pick on him (but for the peppers) but other people really gave him hell. At the time I just didn't have the patience to deal with his oddness and tried to stay away as much as possible, meaning I didn't go out of my way to make friends with him but if he talked to me I wasn't mean to him either. I didn't understand how he could cry like a baby from someone stepping on his foot on accident like happens sometimes. Boggled my mind Looking back on it all now, thinking about how he was, that boy was definatly autistic. That incident when someone accidently stepped on his foot I now see as a SI problem. I remember someone once put a sign on his back that said " Watch out for falling lice " . Well, you know kid humor, that is funny. Anyway, this guy that I sat next to in study hall, Bell, really went out of his way to try and be nice to but he also found funny for some reason and didn't understand when he did something that just make laugh and would always get to do something over and over to provide him with amusement. Anyway, sat in front of us in study hall. seen that sign and was laughing hysterically and told that there was something on his back, took it off because was doing that weird trying to turn his head 180 degrees to either side thing to see it, and just crumpled it up and tossed it out. never seen it but spent most of study hall laughing, Those are the two incidents that I remember the best. Well, then there was 6th grade and Mr Vozar. That man was just an asshole. Complete and total asshole. He used to pick on worse than any of the kids. His theory was that he was " toughing him up " and " teaching him how to take it " . I always wished that he would just leave him alone. I mean, the man put him in tears (and it is very odd seeing a 6 foot kid crying) where he had to leave class several times. I have no idea why I just went on about this.... Georga Visit my new web page at www.ubahbookshelf.com This tag line space for rent. Re: The cotinuing march toward diagnosis > > > > Sweetie - > > > > If he goes into a special education class it does not by any means > classify > > him as anything other than what he is now - a child with challenges. I > > always thought was subtle too. Now that I see her with typical > > children it's as obvious as an a red light. (But remember she only needed > > the special ed class for 6 months). When you're home you are comparing him > to > > himself before any services. When you're in school you're comparing him > to > > the other children. That's how he will make progress - by determining > where > > he needs the extra help weather it's turntaking, pragmatic langauge or > > pretend play. > > > > Extra services will not hurt him as long as he's in the proper placement > for > > HIM. My best friend's son has been with services for 2 1/2 years and she > is > > just now coming to terms with the diagnois. You don't have to send out a > > card that says My Son is in Special Education - you don't even have to > tell > > anyone. That's a personal choice. I'm sorry that your family is not > being > > supportive... mine isn't really either and it sucks. > > > > Hugs > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 The short bus. LOL! Sorry. Where and I grew up the short bus was a joke. I mean, they were supposed to be the sped kids but where we were sped ment the kids that no one wanted to deal with. You know, the problem cases, not necessary the sped cases. The kids that had an attitude about school and were failing because they didn't do their work and they dumped them in, what we always refered to as " the retarded class " . Now, the one school that I went to sped was just that sped. The kids with various learning problems were in there, not the ones that didn't want to be in school and do work. And they didn't ride the " short bus " . We didn't have a short bus for that district. The sped was right in the school, the classroom was on the bottom floor down from the caffateria (there weren't any other classrooms down there but the gym, the TAG room and the art room. The kids in sped stayed in that room from K through 6 and the teacher in there was great with them. There were one or two kids that weren't in sped that should have been but they did just fine in regular classes. ended up in sped adventually. When we moved up to the jr high there was a sped room there was well that these kids spent most of their time in. on the other hand.... I feel so bad about how he was treated now knowing what I know now about autism. was a really tall and big kid even in 6th grade. In 7th he was like 6 feet tall. The one thing that I picked on him about was the green pepper strips that he had to have in his lunch every day. Did not understand how anyone could eat them (then again, at the time they gave me heartburn. LOL). Anyway, he was this huge kid and had the emotional materity of a kindergartner. He was really easy for people to pick on. I didn't really pick on him (but for the peppers) but other people really gave him hell. At the time I just didn't have the patience to deal with his oddness and tried to stay away as much as possible, meaning I didn't go out of my way to make friends with him but if he talked to me I wasn't mean to him either. I didn't understand how he could cry like a baby from someone stepping on his foot on accident like happens sometimes. Boggled my mind Looking back on it all now, thinking about how he was, that boy was definatly autistic. That incident when someone accidently stepped on his foot I now see as a SI problem. I remember someone once put a sign on his back that said " Watch out for falling lice " . Well, you know kid humor, that is funny. Anyway, this guy that I sat next to in study hall, Bell, really went out of his way to try and be nice to but he also found funny for some reason and didn't understand when he did something that just make laugh and would always get to do something over and over to provide him with amusement. Anyway, sat in front of us in study hall. seen that sign and was laughing hysterically and told that there was something on his back, took it off because was doing that weird trying to turn his head 180 degrees to either side thing to see it, and just crumpled it up and tossed it out. never seen it but spent most of study hall laughing, Those are the two incidents that I remember the best. Well, then there was 6th grade and Mr Vozar. That man was just an asshole. Complete and total asshole. He used to pick on worse than any of the kids. His theory was that he was " toughing him up " and " teaching him how to take it " . I always wished that he would just leave him alone. I mean, the man put him in tears (and it is very odd seeing a 6 foot kid crying) where he had to leave class several times. I have no idea why I just went on about this.... Georga Visit my new web page at www.ubahbookshelf.com This tag line space for rent. Re: The cotinuing march toward diagnosis > > > > Sweetie - > > > > If he goes into a special education class it does not by any means > classify > > him as anything other than what he is now - a child with challenges. I > > always thought was subtle too. Now that I see her with typical > > children it's as obvious as an a red light. (But remember she only needed > > the special ed class for 6 months). When you're home you are comparing him > to > > himself before any services. When you're in school you're comparing him > to > > the other children. That's how he will make progress - by determining > where > > he needs the extra help weather it's turntaking, pragmatic langauge or > > pretend play. > > > > Extra services will not hurt him as long as he's in the proper placement > for > > HIM. My best friend's son has been with services for 2 1/2 years and she > is > > just now coming to terms with the diagnois. You don't have to send out a > > card that says My Son is in Special Education - you don't even have to > tell > > anyone. That's a personal choice. I'm sorry that your family is not > being > > supportive... mine isn't really either and it sucks. > > > > Hugs > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 By the holidays, I imagine the people you care enough about to want to tell will probably know. If you write up newsletters, you could tell how he's doing in his various therapys if you want, it's entirely up to you. Sue Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 > > Yes, I don't know how I'm going to handle this either. I mean, around the > holidays, do you send out the usual cards with little letters casually > mentioning that your child was dx as autistic? Is that weird? > > (SAHM in GA) , this is EXACTLY what I did with extended family and friends out of my area. I wrote it in my holiday letter. Brandt was dxed in May, 2001 so I had lots of time to formulate words before Christmas. E-mail me off list and I'll send you a copy of the letter I wrote if you want me to. Leggs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 >>>>>>>>>>> I mean, around the holidays, do you send out the usual cards with little letters casually mentioning that your child was dx as autistic? Is that weird? >>>>>>>>>>> I've gotten cards like that. And no, I don't think it's weird. I prefer letters that are honest instead of those missives where people pump up their lives and brag about everything. I don't send a newsletter anymore, mainly because it just takes to much time. Now I just enclose a pic of the kids in a christmas card and leave it at that. Tuna ===== mom to: , 8, ASD , 4, NT Normal is just a setting on the washing machine. - Whoopi Goldberg ______________________________________________________________________ Post your free ad now! http://personals.yahoo.ca Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 >>>>>>>>>>> I mean, around the holidays, do you send out the usual cards with little letters casually mentioning that your child was dx as autistic? Is that weird? >>>>>>>>>>> I've gotten cards like that. And no, I don't think it's weird. I prefer letters that are honest instead of those missives where people pump up their lives and brag about everything. I don't send a newsletter anymore, mainly because it just takes to much time. Now I just enclose a pic of the kids in a christmas card and leave it at that. Tuna ===== mom to: , 8, ASD , 4, NT Normal is just a setting on the washing machine. - Whoopi Goldberg ______________________________________________________________________ Post your free ad now! http://personals.yahoo.ca Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 People make jokes about the Handi-bus? The nerve! Grrrr. Tuna ... who's feeling the urge to smack someone >>>>>>>>>>>>>>> > Thanks, . I know you're right. It just seems > like every week I hear a > " short bus " joke somewhere, and that makes special > education seem like such > a stigma. I guess I'm going to have to toughen up > about it : ) > >>>>>>>>>>>>>>>>>>> ===== mom to: , 8, ASD , 4, NT Normal is just a setting on the washing machine. - Whoopi Goldberg ______________________________________________________________________ Post your free ad now! http://personals.yahoo.ca Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2003 Report Share Posted May 8, 2003 People make jokes about the Handi-bus? The nerve! Grrrr. Tuna ... who's feeling the urge to smack someone >>>>>>>>>>>>>>> > Thanks, . I know you're right. It just seems > like every week I hear a > " short bus " joke somewhere, and that makes special > education seem like such > a stigma. I guess I'm going to have to toughen up > about it : ) > >>>>>>>>>>>>>>>>>>> ===== mom to: , 8, ASD , 4, NT Normal is just a setting on the washing machine. - Whoopi Goldberg ______________________________________________________________________ Post your free ad now! http://personals.yahoo.ca Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 9, 2003 Report Share Posted May 9, 2003 I think in retrospect we can all identify someone we went to school with who was on the spectrum. Unfortunately, I can't think of many instances where these individuals were treated very well. I wonder if things are any better now ... or if they will get better as more spectrum children are funnled through the system ... (SAHM in GA) MSN elizabethloht@... n 33, mo, no formal dx Phoebe, 12 weeks Re: The cotinuing march toward diagnosis > > > > > > > Sweetie - > > > > > > If he goes into a special education class it does not by any means > > classify > > > him as anything other than what he is now - a child with challenges. I > > > always thought was subtle too. Now that I see her with typical > > > children it's as obvious as an a red light. (But remember she only > needed > > > the special ed class for 6 months). When you're home you are comparing > him > > to > > > himself before any services. When you're in school you're comparing him > > to > > > the other children. That's how he will make progress - by determining > > where > > > he needs the extra help weather it's turntaking, pragmatic langauge or > > > pretend play. > > > > > > Extra services will not hurt him as long as he's in the proper placement > > for > > > HIM. My best friend's son has been with services for 2 1/2 years and > she > > is > > > just now coming to terms with the diagnois. You don't have to send out > a > > > card that says My Son is in Special Education - you don't even have to > > tell > > > anyone. That's a personal choice. I'm sorry that your family is not > > being > > > supportive... mine isn't really either and it sucks. > > > > > > Hugs > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 9, 2003 Report Share Posted May 9, 2003 In a message dated 5/8/03 11:00:32 AM Eastern Daylight Time, elizabeth.loht@... writes: > " short bus " joke somewhere now I follow the bus so that I can find new friends LOL, Just kidding I drive myself. Hang in there wendy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 9, 2003 Report Share Posted May 9, 2003 In a message dated 5/8/03 11:00:32 AM Eastern Daylight Time, elizabeth.loht@... writes: > " short bus " joke somewhere now I follow the bus so that I can find new friends LOL, Just kidding I drive myself. Hang in there wendy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2003 Report Share Posted May 10, 2003 Wishing you big hugs , I too felt that way. Relieved that we got the dx, not all that upset at the time and yet dreading it at the same time. Like having part of your heart ripped out. Thinking of you all. Jen Quote Link to comment Share on other sites More sharing options...
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