Guest guest Posted March 29, 2001 Report Share Posted March 29, 2001 I don't mean to be rude or anything, but why in the world do you keep him in this school? They sound like monsters.I know where I live I can chose to send my child to any public school I am willing to transport her to based on what I feel like her needs are. If he is not having to be restrained at home I'd be ready to kick some butt over all the restraining they are doing at this place. Jay-regression begining to subside- MD diagnoised SAD > Just a quick up date, after staying home a week on > advice from the doctor, Jay is doing better, I didnt > realize corn was in table salt, so we have eliminated > that, corn is definitely an issue for him, looking > back over the last four years, the doctor felt there > was enough evidence to diagnosis SAD- season affect > disorder and and has prescribed a fullspectrum light > for the classroom- our IEP meeting was postponed until > April 2- I am sure it will be a nightmare, the school > still doesnt understand that it could be possible to > descalate when he is regressed rather than > allowing him to become outrageously aggressive. They > insist that he doesnt need a one on one, but still > doesnt have consistent one on one when he regresses > doing school work that fustrates him or when meds > wane. We are asking for a functional behavior > assement and behavior plan, a new evalution to > identify a possibe learning delay, a technological > assistance eval, a sensory dsyfuction eval, a > consultant in this area familiar with the diet and > PDD, more training for staff regarding autism, I met > with them last week with an advocate present - the > teacher, two counselors, two 'aides', the special ed > director, the BOCES special ed program director and > the trust program director. The said at the meeting > that they knew Jay could write when he wanted to > because in the morning he would dilly with an > assignment for 40min, after lunch when told he had to > finish same assignment to earn computor it took five > minutes, when the advocate an I asked to change > computor time to immediately follow assignment, they > said 'Why would we do that? " (remember these > assignments often lead to regression, then aggression, > then restraint!) I was ALMOST speachless- finally, > their special ed director relented and agreed that > that could be done, and finally they agreed for just > this week-- until the meeting --that one counsellor > would sit with Jay and read to him when he begins to > regress (as I have been asking all along) -- however > in reality that has not happened this week, because > they have not consistently had the man power to do > that. He has been restrained three times. If it > worked, they would agree to a 1/1 aide. They called > the preventative worker, the one I have insisted the > county provide for the last 6 years, and told her I > kept Jay home for a week, forgot to mention that I had > the doctor's permission, she told me they told her > that they felt their program was designed to manage > these issues and I was making it harder for Jay to > adjust this way. This same counsellor who shared this > with her, is the one who refuses to acknowledge the > validity of the diet and the relationship between > regression, aggression, and PDD/NOS w/ autistic like > symptoms! The same person who has not arranged a > meeting with Jays psychiatrist like she was supposed > to for the last month!! At the meeting last week I > discovered our school district special ed director was > lead to believe that I was still restraining Jay!! Jay > was arguing with them that I didnt allow restraint > face down, only face up- Jay hasn't been restrained at > home scince he came home from the hospital and I made > it a priority in this house that every day would be a > restraint free day for jay and that is his number one > goal each day- even before the diet over a year ago!! > Thsi meeting should be very interesting. The advocate > has promised to attend with me. > > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2001 Report Share Posted March 29, 2001 Just a quick up date, after staying home a week on advice from the doctor, Jay is doing better, I didnt realize corn was in table salt, so we have eliminated that, corn is definitely an issue for him, looking back over the last four years, the doctor felt there was enough evidence to diagnosis SAD- season affect disorder and and has prescribed a fullspectrum light for the classroom- our IEP meeting was postponed until April 2- I am sure it will be a nightmare, the school still doesnt understand that it could be possible to descalate when he is regressed rather than allowing him to become outrageously aggressive. They insist that he doesnt need a one on one, but still doesnt have consistent one on one when he regresses doing school work that fustrates him or when meds wane. We are asking for a functional behavior assement and behavior plan, a new evalution to identify a possibe learning delay, a technological assistance eval, a sensory dsyfuction eval, a consultant in this area familiar with the diet and PDD, more training for staff regarding autism, I met with them last week with an advocate present - the teacher, two counselors, two 'aides', the special ed director, the BOCES special ed program director and the trust program director. The said at the meeting that they knew Jay could write when he wanted to because in the morning he would dilly with an assignment for 40min, after lunch when told he had to finish same assignment to earn computor it took five minutes, when the advocate an I asked to change computor time to immediately follow assignment, they said 'Why would we do that? " (remember these assignments often lead to regression, then aggression, then restraint!) I was ALMOST speachless- finally, their special ed director relented and agreed that that could be done, and finally they agreed for just this week-- until the meeting --that one counsellor would sit with Jay and read to him when he begins to regress (as I have been asking all along) -- however in reality that has not happened this week, because they have not consistently had the man power to do that. He has been restrained three times. If it worked, they would agree to a 1/1 aide. They called the preventative worker, the one I have insisted the county provide for the last 6 years, and told her I kept Jay home for a week, forgot to mention that I had the doctor's permission, she told me they told her that they felt their program was designed to manage these issues and I was making it harder for Jay to adjust this way. This same counsellor who shared this with her, is the one who refuses to acknowledge the validity of the diet and the relationship between regression, aggression, and PDD/NOS w/ autistic like symptoms! The same person who has not arranged a meeting with Jays psychiatrist like she was supposed to for the last month!! At the meeting last week I discovered our school district special ed director was lead to believe that I was still restraining Jay!! Jay was arguing with them that I didnt allow restraint face down, only face up- Jay hasn't been restrained at home scince he came home from the hospital and I made it a priority in this house that every day would be a restraint free day for jay and that is his number one goal each day- even before the diet over a year ago!! Thsi meeting should be very interesting. The advocate has promised to attend with me. __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2001 Report Share Posted March 29, 2001 , thank you for verbalizing what my heart has been aching to scream, but this is the only school program available with-in driving range trained to manange aggressive behaviors- it is a day treatment program in an elementary school- the hospital recomended it last year. Its an hour drive for him on the bus every morning. I don't think I could manage his behaviors sucessfully and maintain my sanity if he was home 24 seven- and I am certain he wouldnt learn as much. If this doesnt resolve it's self soon, I may need to home school, but I dont know how and work full time. All his prime time learning windows happen while I am at work. He went months and months and months without restaint- its just that he became intollerant of corn and he severly regresses feb/march/ early april every year!! So we keep working on the school, when he's not regressed he has an incredible relationship with his teacher- (not the counsellor who usually doesnt have that much to do with him because she works in two programs)- and during the summer school, he absolutely loves school, last summer his teacher there- who will be returning this summer, did The sign of the Beaver, only the school is out in the woods so the class dirt biked into the woods every day , built a minuture cabin and recreated the book reading it there. Jay had never even read outloud in a group of children before last summer! Every friday they go to our state park and picnic, hike, bike and swim! And it is six weeks of pure bliss for us! Amazingly- the same program directors run that program! --- renee schlotzhauer renee1dat@...> wrote: > I don't mean to be rude or anything, but why in the > world do you keep him in > this school? __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 30, 2001 Report Share Posted March 30, 2001 Remember that Jay is entitled to a Free and Appropriate Public Education (FAPE). If he is expelled form school, they MUST provide a FAPE for him. Even if it means sending a teacher to your home to teach him. Or paying for him to attend a private school. It's the law! Maureen Quote Link to comment Share on other sites More sharing options...
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