Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 Hi my cyber friends, I just came back fresh from my IEP meeting about Rochelle. There were a few issues we need to go back to the table with and I need your advice. For those of you who have children that don't like to write/cut this question is for you all. Rochelle requires OT services and gets about 1 hour a week. I want her to have cutting and writing daily even though the team does not think she is developmentally ready for it. They are doing other things to get to this level but don't want to push her in this area since it would be hand over hand. I will add that she may be non-compliant. It has been on her IEP for 1/2 a year and not worked on. Rochelle is hyper sensitive in her hands and I just want them to have her work on it for even 10 seconds to acclimate her to the process. Work on longer times and reward her for her efforts. The OT thinks this will turn her off writing and will make it worse when she gets older. I am sure for some kids this has happened and it is a fine line on how much to push the child. If it were up to Rochelle she would never pick up a crayon or chalk unless she wants to chew on it. Her grasp is immature but that did not stop me from teaching her how to feed herself with a spoon. We are progressing but not there yet. She no longer throws the utensil and will scoop repeatedly. There is no right or wrong answer but I asked them when they thought she would be ready and they said, we don't know that. Neither do I. Have any of you had success in this area or failure. I know there are a lot of DS kids who love to write/color/cut but Rochelle isn't one of them. They also gave me a surprise with the Physical Therapy. The PT was not there but wrote a statement that she thought Rochelle functioned fine and didn't need her services. I just fought this battle 6 months ago at eligibility and won but because Rochelle got a new eligibility label she is trying to take this away again. I've called the Sped director but I am tired of them saying only kids with physical disabilities who can't walk independently need PT. Medical vs Theraputic model blah blah blah. This particular PT may not be that good but she may get a better PT next time that will truly work with her. Rochelle is not independently walking up/down stairs, running, jumping etc...and her IEP goals were not being worked on because the PT thought they were inappopriate. Diane (mom to Rochelle 5 1/2 and Danny 7) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 In a message dated 2/22/02 5:14:32 PM Eastern Standard Time, outerspace@... writes: > First, I would use the " parent attachment " to document the situation. > Is there a way that Rochelles doc can write a prescription for pt?? > Thanks Kathy, I already had a doctors perscription in March of 2000. I think I will stick to my guns with this. I will use the info you provided. I just hate having to continue to fight for services that should be a given. Rochelle's potential to achieve these goals will happen. I would like to make it happen sooner with help from PT. I also know other children with lesser gross motor problems getting Physical therapy. It is so subjective. I have already called the Director of Sped and waiting for call back. Diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 Thanks, . I think they just want to wait. Diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 Hi Diane First, I would use the " parent attachment " to document the situation. Is there a way that Rochelles doc can write a prescription for pt?? <<< Physical Therapy is provided to a child or youth with a disability following referral from a physician and, in some states, from school nurses, teachers, occupational therapists, and other professionals. Physical therapists: -- provide treatment to increase muscle strength, mobility, and endurance; -- focus on gross motor skills that rely on the large muscles of the body involved in physical movement and range of motion; -- help to improve the student's posture, gait, and body awareness; and -- monitor the function, fit, and proper use of mobility aids and devices. In relation to special education, physical therapists are primarily concerned with developing and enhancing the physical potential of students with disabilities, so that they can achieve maximum independence and function in all their educational activities>>> to be continued. . . Kathy Re: fine motor - writing -horizontal/vertical Hi my cyber friends, I just came back fresh from my IEP meeting about Rochelle. There were a few issues we need to go back to the table with and I need your advice. For those of you who have children that don't like to write/cut this question is for you all. Rochelle requires OT services and gets about 1 hour a week. I want her to have cutting and writing daily even though the team does not think she is developmentally ready for it. They are doing other things to get to this level but don't want to push her in this area since it would be hand over hand. I will add that she may be non-compliant. It has been on her IEP for 1/2 a year and not worked on. Rochelle is hyper sensitive in her hands and I just want them to have her work on it for even 10 seconds to acclimate her to the process. Work on longer times and reward her for her efforts. The OT thinks this will turn her off writing and will make it worse when she gets older. I am sure for some kids this has happened and it is a fine line on how much to push the child. If it were up to Rochelle she would never pick up a crayon or chalk unless she wants to chew on it. Her grasp is immature but that did not stop me from teaching her how to feed herself with a spoon. We are progressing but not there yet. She no longer throws the utensil and will scoop repeatedly. There is no right or wrong answer but I asked them when they thought she would be ready and they said, we don't know that. Neither do I. Have any of you had success in this area or failure. I know there are a lot of DS kids who love to write/color/cut but Rochelle isn't one of them. They also gave me a surprise with the Physical Therapy. The PT was not there but wrote a statement that she thought Rochelle functioned fine and didn't need her services. I just fought this battle 6 months ago at eligibility and won but because Rochelle got a new eligibility label she is trying to take this away again. I've called the Sped director but I am tired of them saying only kids with physical disabilities who can't walk independently need PT. Medical vs Theraputic model blah blah blah. This particular PT may not be that good but she may get a better PT next time that will truly work with her. Rochelle is not independently walking up/down stairs, running, jumping etc...and her IEP goals were not being worked on because the PT thought they were inappopriate. Diane (mom to Rochelle 5 1/2 and Danny 7) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 I think all kids need to have writting, etc. in their daily school life. It's important it develps so much when they use writting- and I don't think that it should be taken away in any case. I hope that they or you can figure out a way on getting the writting into her school life. . no matter how hard you try. Don't give up. --- dben937342@... wrote: > Hi my cyber friends, > > I just came back fresh from my IEP meeting about > Rochelle. There were a few > issues we need to go back to the table with and I > need your advice. > > For those of you who have children that don't like > to write/cut this question > is for you all. Rochelle requires OT services and > gets about 1 hour a week. I > want her to have cutting and writing daily even > though the team does not > think she is developmentally ready for it. They are > doing other things to get > to this level but don't want to push her in this > area since it would be hand > over hand. I will add that she may be non-compliant. > It has been on her IEP > for 1/2 a year and not worked on. Rochelle is hyper > sensitive in her hands > and I just want them to have her work on it for even > 10 seconds to acclimate > her to the process. Work on longer times and reward > her for her efforts. > > The OT thinks this will turn her off writing and > will make it worse when she > gets older. I am sure for some kids this has > happened and it is a fine line > on how much to push the child. > > If it were up to Rochelle she would never pick up a > crayon or chalk unless > she wants to chew on it. Her grasp is immature but > that did not stop me from > teaching her how to feed herself with a spoon. We > are progressing but not > there yet. She no longer throws the utensil and will > scoop repeatedly. > > There is no right or wrong answer but I asked them > when they thought she > would be ready and they said, we don't know that. > Neither do I. Have any of > you had success in this area or failure. I know > there are a lot of DS kids > who love to write/color/cut but Rochelle isn't one > of them. > > They also gave me a surprise with the Physical > Therapy. The PT was not there > but wrote a statement that she thought Rochelle > functioned fine and didn't > need her services. I just fought this battle 6 > months ago at eligibility and > won but because Rochelle got a new eligibility label > she is trying to take > this away again. I've called the Sped director but I > am tired of them saying > only kids with physical disabilities who can't walk > independently need PT. > Medical vs Theraputic model blah blah blah. This > particular PT may not be > that good but she may get a better PT next time that > will truly work with > her. Rochelle is not independently walking up/down > stairs, running, jumping > etc...and her IEP goals were not being worked on > because the PT thought they > were inappopriate. > Diane (mom to Rochelle 5 1/2 and Danny 7) > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 your welcome, I didn't know that I was any help --- dben937342@... wrote: > Thanks, . I think they just want to wait. > Diane > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 your welcome, I didn't know that I was any help --- dben937342@... wrote: > Thanks, . I think they just want to wait. > Diane > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 my naty guy is like your rochelle, wont color, write etc. he is 10yrs now and just now starting to be able to write his first name sort of legibly, but he can type pecking very well, i would start implementing these type of things such as rubber stamp for names and words, keyboarding, intellikeys, and continue a short block of handwriting/cutting OT stuff dly, this way she isnt held back just cause she cant write. shawna. Re: fine motor - writing -horizontal/vertical Hi my cyber friends, I just came back fresh from my IEP meeting about Rochelle. There were a few issues we need to go back to the table with and I need your advice. For those of you who have children that don't like to write/cut this question is for you all. Rochelle requires OT services and gets about 1 hour a week. I want her to have cutting and writing daily even though the team does not think she is developmentally ready for it. They are doing other things to get to this level but don't want to push her in this area since it would be hand over hand. I will add that she may be non-compliant. It has been on her IEP for 1/2 a year and not worked on. Rochelle is hyper sensitive in her hands and I just want them to have her work on it for even 10 seconds to acclimate her to the process. Work on longer times and reward her for her efforts. The OT thinks this will turn her off writing and will make it worse when she gets older. I am sure for some kids this has happened and it is a fine line on how much to push the child. If it were up to Rochelle she would never pick up a crayon or chalk unless she wants to chew on it. Her grasp is immature but that did not stop me from teaching her how to feed herself with a spoon. We are progressing but not there yet. She no longer throws the utensil and will scoop repeatedly. There is no right or wrong answer but I asked them when they thought she would be ready and they said, we don't know that. Neither do I. Have any of you had success in this area or failure. I know there are a lot of DS kids who love to write/color/cut but Rochelle isn't one of them. They also gave me a surprise with the Physical Therapy. The PT was not there but wrote a statement that she thought Rochelle functioned fine and didn't need her services. I just fought this battle 6 months ago at eligibility and won but because Rochelle got a new eligibility label she is trying to take this away again. I've called the Sped director but I am tired of them saying only kids with physical disabilities who can't walk independently need PT. Medical vs Theraputic model blah blah blah. This particular PT may not be that good but she may get a better PT next time that will truly work with her. Rochelle is not independently walking up/down stairs, running, jumping etc...and her IEP goals were not being worked on because the PT thought they were inappopriate. Diane (mom to Rochelle 5 1/2 and Danny 7) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 my naty guy is like your rochelle, wont color, write etc. he is 10yrs now and just now starting to be able to write his first name sort of legibly, but he can type pecking very well, i would start implementing these type of things such as rubber stamp for names and words, keyboarding, intellikeys, and continue a short block of handwriting/cutting OT stuff dly, this way she isnt held back just cause she cant write. shawna. Re: fine motor - writing -horizontal/vertical Hi my cyber friends, I just came back fresh from my IEP meeting about Rochelle. There were a few issues we need to go back to the table with and I need your advice. For those of you who have children that don't like to write/cut this question is for you all. Rochelle requires OT services and gets about 1 hour a week. I want her to have cutting and writing daily even though the team does not think she is developmentally ready for it. They are doing other things to get to this level but don't want to push her in this area since it would be hand over hand. I will add that she may be non-compliant. It has been on her IEP for 1/2 a year and not worked on. Rochelle is hyper sensitive in her hands and I just want them to have her work on it for even 10 seconds to acclimate her to the process. Work on longer times and reward her for her efforts. The OT thinks this will turn her off writing and will make it worse when she gets older. I am sure for some kids this has happened and it is a fine line on how much to push the child. If it were up to Rochelle she would never pick up a crayon or chalk unless she wants to chew on it. Her grasp is immature but that did not stop me from teaching her how to feed herself with a spoon. We are progressing but not there yet. She no longer throws the utensil and will scoop repeatedly. There is no right or wrong answer but I asked them when they thought she would be ready and they said, we don't know that. Neither do I. Have any of you had success in this area or failure. I know there are a lot of DS kids who love to write/color/cut but Rochelle isn't one of them. They also gave me a surprise with the Physical Therapy. The PT was not there but wrote a statement that she thought Rochelle functioned fine and didn't need her services. I just fought this battle 6 months ago at eligibility and won but because Rochelle got a new eligibility label she is trying to take this away again. I've called the Sped director but I am tired of them saying only kids with physical disabilities who can't walk independently need PT. Medical vs Theraputic model blah blah blah. This particular PT may not be that good but she may get a better PT next time that will truly work with her. Rochelle is not independently walking up/down stairs, running, jumping etc...and her IEP goals were not being worked on because the PT thought they were inappopriate. Diane (mom to Rochelle 5 1/2 and Danny 7) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 In a message dated 2/22/02 11:11:57 PM Eastern Standard Time, greenpak@... writes: > i would start implementing these type of things such as rubber stamp for > names and words, keyboarding, intellikeys, and continue a short block of > handwriting/cutting OT stuff dly, this way she isnt held back just cause > she cant write. shawna. > a, What are intellikeys? Thanks for the imput. Diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 In a message dated 2/22/02 11:11:57 PM Eastern Standard Time, greenpak@... writes: > i would start implementing these type of things such as rubber stamp for > names and words, keyboarding, intellikeys, and continue a short block of > handwriting/cutting OT stuff dly, this way she isnt held back just cause > she cant write. shawna. > a, What are intellikeys? Thanks for the imput. Diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 In a message dated 2/22/2002 11:12:06 PM Eastern Standard Time, greenpak@... writes: > They also gave me a surprise with the Physical Therapy. The PT was not there > > but wrote a statement that she thought Rochelle functioned fine and > didn't > need her services. I just fought this battle 6 months ago at eligibility > and > won but because Rochelle got a new eligibility label she is trying to > take > this away again. I've called the Sped director but I am tired of them > saying > only kids with physical disabilities who can't walk independently need > PT. > Medical vs Theraputic model blah blah blah. This particular PT may not be > > that good but she may get a better PT next time that will truly work with > > her. Rochelle is not independently walking up/down stairs, running, > jumping > etc...and her IEP goals were not being worked on because the PT thought > they > were inappopriate. > We had the same problem with Trisha, they said she didn't need PT because she could get around the school, even though sometimes she had some problems. What I did was request that they put her on as a consult once a month for 15 mins. Well at the next IEP meeting the PT announced that she was spending more time with Trisha as she felt Trisha needed more work so now we have PT once a week for 1/2 hour. I don't know if it will work for you but you might want to suggest consultative pt for awhile. We have a new IEP meeting scheduled this coming Tues. so we will see how the PT has been doing. I know they say Trisha won't cooperate in PE, but they don't know why. I am still fighting for a one-on-one aid, I have had Trisha observed several times with the autism program in her class and both the consultants and I agree that she would benefit from a one on one aid. Even though Trisha is making progress this year, slow but sure, we feel that because she is so far behind that an aid could help work with her when the teacher is working with the other students instead of just letting her play. The autism consultant said that if she had an aid that they could teach her to work more independantly instead of having so much free time. The consultant said that Trisha needs structured activities constantly. The school says because the class only has 3 kids they don't feel an aid is needed for Trisha, they only have an aid part time for her class and she spends most of that time working in the cafeteria. The consultant said we weren't concerned about how big the class was, we were concerned about Trisha's needs. So if anyone has any input that could help me make a case for a one on one aid please let me know. Trisha is the only one in her class that is non-verbal, can't read, can't write and will wander off if given half a chance. THanks, Carol aka Trishasmom She isn't Typical, She's Trisha! <A HREF= " http://hometown.aol.com/csvillars/trishapage.htm " >Trisha's Pooh Page</A> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2002 Report Share Posted February 23, 2002 In a message dated 2/23/02 7:37:28 AM Eastern Standard Time, Csvillars@... writes: > . I am still > fighting for a one-on-one aid, I have had Trisha observed several times > with > the autism program in her class and both the consultants and I agree that > she > would benefit from a one on one aid. Even though Trisha is making progress > > this year, slow but sure, we feel that because she is so far behind that an > > aid could help work with her when the teacher is working with the other > students instead of just letting her play. The autism consultant said that > > if she had an aid that they could teach her to work more independantly > instead of having so much free time. The consultant said that Trisha needs > > structured activities constantly. Wow, Trisha seems just like Rochelle. I feel Rochelle has to much play time too. The teacher can't possibly be with our kids full-time because of the other kids needs. I feel the same way about Rochelle's needs not being met because the school just doesn't do that. (have one-on-one aid in self-contained class) I hope you get some answers. Diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2002 Report Share Posted February 23, 2002 In a message dated 2/22/2002 4:06:31 PM Eastern Standard Time, dben937342@... writes: > . Rochelle is not independently walking up/down stairs, running, jumping > etc...and her IEP goals were not being worked on because the PT thought > they > were inappopriate. > Hi Diane, If the PT thought the goals were inappropriate then it was up to her to call a PPT to discuss this but as long as they are on her IEP they are law and must be addressed. I would be a fireball. As far as the fine motor,I honestly don't have any answers. I know that Zeb does not write,cut etc. We have been working on this forever and I am so frustrated that I could spit. I just had a private OT eval done and his fine motor is 34-38 mos. I really don't think there has been any improvement since kindergarten. The OT in this district is so ineffective but also I haven't come up with any magic solution either. I work on these things everyday at home. I certainly share your frustration. My question would be what if they are never developmentally ready. The fine motor stays at what it is or what? I was told that once a child with MR reaches about 12 they reach their potential on gross and fine motor skills. I am not sure how true this is but time is running out for us in this area. Charlyne Mom to Zeb 9 DS/OCD ? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2002 Report Share Posted February 23, 2002 In a message dated 2/22/02 4:06:34 PM Eastern Standard Time, dben937342@... writes: > Rochelle is hyper sensitive in her hands Diane, Have you tried a brushing program on Rochelle's hands? That would probably help with the hyper-sensitivity. You need a skilled OT to show you how to do it right. Every finger should be done individually, as well as the palm. <<Rochelle is not independently walking up/down stairs, running, jumping etc...and her IEP goals were not being worked on because the PT thought they were inappopriate.>> Diane, Maddie has not qualified for PT since she was two. But she's been jumping, walking up/down steps since then. And she skips well too. Seems to me that writing in these goals SHOULD guarantee you some PT for her. Push it if you can. Donna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2002 Report Share Posted February 23, 2002 In a message dated 2/22/02 6:43:22 PM Eastern Standard Time, dben937342@... writes: > Thanks Kathy, I already had a doctors perscription in March of 2000. I think > I will stick to my guns with this. Diane, Just check first to make sure that your insurance does not have a cap. Sometimes insurance companies do and you can risk using up your quota. Then if something were to happen to another family member, you would not be able to get services. Donna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2002 Report Share Posted February 23, 2002 In a message dated 2/23/02 11:28:10 AM Eastern Standard Time, charlyne1121@... writes: > My > question would be what if they are never developmentally ready. The fine > motor stays at what it is or what? I was told that once a child with MR > reaches about 12 they reach their potential on gross and fine motor skills. > I > am not sure how true this is but time is running out for us in this area. > Charlyne > Mom to Zeb 9 DS/OCD ? > > > They asked me why I wanted Rochelle to practice drawing lines. Really now. What kind of question is that? I said, " So she can write her name " Duh.... I would keep working on it Charlyne. Rochelle's brother does not like to write either. But we make him do it. He is learning to type which helps frustration. But we still make him write. I hope there is not a magic age where you can't teach them. I for one don't believe there is but it is probably easier to influence them when their younger. What do you think of a wiping the nose goal? This is one the school district came up with. Said it was a social goal. Kids won't hang out with her if she has a runny nose. Like Rochelle cares if other kids pay attention to her? She totally ignores all the kids who try to say hi and interact with her and they keep trying. They said, she doesn't like for them to wipe it. I felt like telling them to just leave her nose alone. But, I know they think it is unhygenic yet they never clean the toys the kids all drool on. Oh, and they forget to wash their hands before eating sometimes. And the washing hands goal has not been worked on even though it was on the IEP. Well, I said, wiping the nose was not a goal I wanted on the IEP and that they can work on it anyway if they want to. Rochelle can't even blow her nose yet. And, she can wipe her nose if you give her the tissue but she usually misses. I let them keep the nose goal but I think I'll get rid of that one in a few weeks. Diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2002 Report Share Posted February 23, 2002 In a message dated 2/23/02 1:05:45 PM Eastern Standard Time, duffey48@... writes: > probably help with the hyper-sensitivity. You need a skilled OT to show > you > how to do it right. Every finger should be done individually, as well as > the palm. > > I have the brushes and will ask OT about this. ( the surgical scrub brushes?) Thanks for the idea. Maddie is way more coordinated then Rochelle. I could tell by your comments about playing ball. She is even better than my 8 yr old son. Diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2002 Report Share Posted February 23, 2002 In a message dated 2/23/02 5:10:52 PM Eastern Standard Time, dben937342@... writes: > I have the brushes and will ask OT about this. ( the surgical scrub brushes?) > Thanks for the idea. Maddie is way more coordinated then Rochelle. I could > tell by your comments about playing ball. She is even better than my 8 yr > old > son. > Diane > Yes, but there are various kinds of brushes. Certain hairbrushes are good to use on the palms of the hands. You can look at them in the sensory catalogs. Yes, Maddie is VERY coordinated. She's better at dribbling a ball than almost any kid her age I have ever come across. However, cognitively, she is years behind even most of the kids on this list. But this just goes to show you that we all have our strengths. Believe me Diane, Maddie's abilities are actually a hindrance around here. She can run SO SO fast!!! Bad for us because we live in the city---she could be on a major street in just seconds (this is why I walk 4 miles a day and have recently started lifting). She has this uncanny climbing ability--bad for us because we have to try and preclude what she'll do next to put herself in danger...we've built contraptions to keep her from hurling herself down stairways. We list her wonderful gross motor skills as a strength, but it's also listed as an area that we need major help with. Donna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2002 Report Share Posted February 23, 2002 In a message dated 2/23/02 5:39:05 PM Eastern Standard Time, duffey48@... writes: > She has this uncanny climbing ability--bad for us because we have > to try and preclude what she'll do next to put herself in danger...we've > built contraptions to keep her from hurling herself down stairways. We > list her wonderful gross motor skills as a strength, but it's also listed > as > an area that we need major help with. > Donna > > > You had mentioned in a earlier post that you broke your neck back a few years ago. Was Maddie climbing on you? Because Rochelle trys to climb up us but I tell her no no because I wouldn' t want to drop her Diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2002 Report Share Posted February 24, 2002 In a message dated 2/22/02 4:05:15 PM US Eastern Standard Time, dben937342@... writes: << For those of you who have children that don't like to write/cut this question is for you all. >> Hi Diane, My son, Gene is 13 and he has never wanted to write or color. His coloring consists of making big circles on a paper iwth a marker or crayon. I remember when he was 5 ot 6 , that I too was told he wasn't ready for writing....now I am not sure he really ever will be. Early on, I set up a goal that he would independently learn to print his own name. For many years, he has copied his name on paper over broken likes that spell his name. I think he can now write most of his name without the broken lines, but this varies. Using his hands for writing is something he has always resisted...for cutting too. I don't think Gene will be a writer, so I have pushed for a number of years now that he learns keyboarding. When I pushed for this in K, I remember the spec ed teacher said he couldn't learn this. He does a pretty good job with this today. He does all his spelling words on the computer...can hear then and then type them. I wish, of course, that he could learn to type his thoughts in sentences, but that hasn't happened yet....but I see this as a much greater possiblity than him ever writing them. Someday, perhaps he will be able to speak his thoughts in sentences, that would be the best. I would encourage you to keep on asking for some writing adn cutting practice, but to really consider keyboarding down the road. Using a tiltboard will help and have her squeeze theraputty to strengthen her hands too. Re: the PT, we didn't get much PT for Gene, same reasoning your staff is giving. It was mainly reserved for the kids with CP or physical disabilities. But in a way, Gene is physically disabled...much of it because of his perceptual problems. EXample: I was setting him and his brother up for camp this summerr. I thought we would try the regular housing this year, vs. special needs housing. We finally put him in nature adventure because the sport camps like soccer, basketball won't work....he will be doing some hiking every day. I told them, as long as it isn't too rocky, uneven or too long. They agreed he could come back with his counselor if it got too tough. When we got to housing, I found his group would be in the chalets which are on stilts and you need to clim a ladder to get to them!! I said " no way " , he is afraid to even climb a ladder into an above ground pool. Open ladders like that just don't work for him...so we had to put him back into the special area for housing. Gene learned to jump when he was about 9 and he really doesn't ride any form of bike. I think PT is worth pursuing and I believe it can be helpful to our kids if they need it. Lauri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2002 Report Share Posted February 24, 2002 In a message dated 2/22/02 4:05:15 PM US Eastern Standard Time, dben937342@... writes: << For those of you who have children that don't like to write/cut this question is for you all. >> Hi Diane, My son, Gene is 13 and he has never wanted to write or color. His coloring consists of making big circles on a paper iwth a marker or crayon. I remember when he was 5 ot 6 , that I too was told he wasn't ready for writing....now I am not sure he really ever will be. Early on, I set up a goal that he would independently learn to print his own name. For many years, he has copied his name on paper over broken likes that spell his name. I think he can now write most of his name without the broken lines, but this varies. Using his hands for writing is something he has always resisted...for cutting too. I don't think Gene will be a writer, so I have pushed for a number of years now that he learns keyboarding. When I pushed for this in K, I remember the spec ed teacher said he couldn't learn this. He does a pretty good job with this today. He does all his spelling words on the computer...can hear then and then type them. I wish, of course, that he could learn to type his thoughts in sentences, but that hasn't happened yet....but I see this as a much greater possiblity than him ever writing them. Someday, perhaps he will be able to speak his thoughts in sentences, that would be the best. I would encourage you to keep on asking for some writing adn cutting practice, but to really consider keyboarding down the road. Using a tiltboard will help and have her squeeze theraputty to strengthen her hands too. Re: the PT, we didn't get much PT for Gene, same reasoning your staff is giving. It was mainly reserved for the kids with CP or physical disabilities. But in a way, Gene is physically disabled...much of it because of his perceptual problems. EXample: I was setting him and his brother up for camp this summerr. I thought we would try the regular housing this year, vs. special needs housing. We finally put him in nature adventure because the sport camps like soccer, basketball won't work....he will be doing some hiking every day. I told them, as long as it isn't too rocky, uneven or too long. They agreed he could come back with his counselor if it got too tough. When we got to housing, I found his group would be in the chalets which are on stilts and you need to clim a ladder to get to them!! I said " no way " , he is afraid to even climb a ladder into an above ground pool. Open ladders like that just don't work for him...so we had to put him back into the special area for housing. Gene learned to jump when he was about 9 and he really doesn't ride any form of bike. I think PT is worth pursuing and I believe it can be helpful to our kids if they need it. Lauri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2002 Report Share Posted February 24, 2002 In a message dated 2/24/02 11:47:33 AM Eastern Standard Time, timothytlstein@... writes: > For many years, he has copied his > name on paper over broken likes that spell his name. I think he can now > write most of his name without the broken lines, but this varies. Using > his > hands for writing is something he has always resisted...for cutting too. I > > don't think Gene will be a writer, so I have pushed for a number of years > now > that he learns keyboarding Thanks Lauri, it was really good to see someone who has gotten the same advice. Glad to hear Gene can write his name. That's all I want right now. Even if it's when she is 13 gosh 18. One step at a time. I am aware of keyboarding, slant boards etc.. because of Rochelle's older brother with the same needs just not the ds. He also resists and will never be a writer on paper but has started keyboarding his thoughts. Not an easy task I agree. Thank you again for the encouragement. Diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2002 Report Share Posted February 24, 2002 In a message dated 2/24/02 11:47:33 AM Eastern Standard Time, timothytlstein@... writes: > For many years, he has copied his > name on paper over broken likes that spell his name. I think he can now > write most of his name without the broken lines, but this varies. Using > his > hands for writing is something he has always resisted...for cutting too. I > > don't think Gene will be a writer, so I have pushed for a number of years > now > that he learns keyboarding Thanks Lauri, it was really good to see someone who has gotten the same advice. Glad to hear Gene can write his name. That's all I want right now. Even if it's when she is 13 gosh 18. One step at a time. I am aware of keyboarding, slant boards etc.. because of Rochelle's older brother with the same needs just not the ds. He also resists and will never be a writer on paper but has started keyboarding his thoughts. Not an easy task I agree. Thank you again for the encouragement. Diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2002 Report Share Posted February 24, 2002 In a message dated 2/23/02 6:45:33 PM Eastern Standard Time, dben937342@... writes: > You had mentioned in a earlier post that you broke your neck back a few > years > ago. Was Maddie climbing on you? Because Rochelle trys to climb up us but I > tell her no no because I wouldn' t want to drop her > Diane Diane, Yes, a disc in my neck ruptured. Spread out over 5 vertebrae. I had lost my reflexes, had spinal chord compression, and came very close to being paralyzed (they did emergency spinal fusion surgery). Scariest time in my life!!! Duff's too. We do think it had a lot to do with my carting Maddie around. She used to just dive on you when you didn't expect it. Now, she absolutely KNOWS not to climb on Mom...I just wont' let her. And we ahve worked diligently on trying to get her to be more independent...it's still work. THings like, having her climb into her car seat instead of being lifted in (we have a suburban and lifting her UP and into that sucker is a major task for a little person like me). I am very cautious now....sure dont' want that experience again!! Donna Quote Link to comment Share on other sites More sharing options...
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