OUr child is finishing up first grade. Due to his struggles with reading, we had him evalauated for an LD. The school took alot of steps and went through a big (if rushed) process and came to the conclusion that he qualified for services under the "other medical impairments" siting, but not diognosing ADHD. We have been in touch with the pediatrition and will be seeking an official confirm or deny from him.
From what I have been reading on the net and these boards, I think it is pretty mild. However, the school has to have an education plan drafted in the next 30 days, which will probably be sooner because school and teachers will be out before then. And it will probably be sooner than the pediatrition can weigh in.
So my question is to all you parents who have been through this. What kinds of things have worked for your children at school, things that the school provides? What should I be trying to get into his plan? Front of the class room, the possibility of an aide.....what else?
Thanks so much.
From what I have been reading on the net and these boards, I think it is pretty mild. However, the school has to have an education plan drafted in the next 30 days, which will probably be sooner because school and teachers will be out before then. And it will probably be sooner than the pediatrition can weigh in.
So my question is to all you parents who have been through this. What kinds of things have worked for your children at school, things that the school provides? What should I be trying to get into his plan? Front of the class room, the possibility of an aide.....what else?
Thanks so much.
My DS6 had ADHD and we found that medication did very well for him. He couldn't swallow any of the pills and is on a patch much like for smokers. At school we do many things to help him


) everyone involved wanted her on meds, but us. We e-schooled at the time (virtual charter school, so it was a public school, but at home). All of the IEP folks, the OT, everyone kept asking when she was going to start meds. We kept explaining that we were NOT going to put her on meds and we got the hands tossed up, there's only so much we can do attitude. I could NOT believe the things that were said.
The cushion keeps their core making small movements to keep them steady which drains some of the energy. She also has yoga exercises she can do to both speed up or slow down. Frequent breaks and longer times to do the work were important on her IEP. She also swings a lot, to the point where we are putting a chair swing in our basement play room. 