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My son is almost 3 and in California that is when his services are turned over to the school district. I've heard of all sorts of problems from my friends who have had to fight with the districts to get there special need's kids services but i have never heard from the parent of a child with NF. I know that symptoms vary, and policy's very. But i am wondering what you guys have done with your kids in regards to school and special education?
I'm really just trying to get him speech. He's come a long way with his PT (he still falls more than most kids but he's an excellent climber and can do just about everything but jump with both feet. But it is his ability to communicate with other people besides his mom that concerns me.
