Autism and Epilepsy

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Perhaps because there wasn't as much of an awareness of Aspergers 30 or 40 years ago?
Also...in our case our son hasn't been officially diagnosed with autism...perhaps because everytime we see any specialist we're having to deal with so many other things, and not sure what difference having an official diagnosis would make. I think his school therapists feel he is autistic (they have made it clear that they don't think he will ever regain his lost speech -- while I haven't yet given up that battle) but they haven't said so directly, just hinted.
 
My kids were both born with autism. Neither have epilepsy but I have an old diagnosis of E myself...
 
Karen, it does make a difference if your son is officially diagnosed with Autism. Insurance will pay for many therapies, most important for your son would be speech. I know schools provide that service to kids, but to be honest, it is just marginal in quality for the most part. There are many speech pathologist your insurance will pay for that are wonderful! They have more resources available to them. Childrens hospitals are especially wonderful for their speech programs for children. Check into it. You will be hearing your sons beautiful voice again, dont give up!
 
Well, he's already been diagnosed with Down Syndrome and Seizure Disorder, so qualifies for speech and other therapies anyway.

In the beginning, the school told us he didn't qualify for speech therapy. Huh? He doesn't speak! How can he not qualify? Well, it had something to do with their testing showed that his "expressive" speech and "receptive" speech were at the same levels. In other words, in their minds, he wasn't speaking because he was too cognitively impaired to understand language, let alone speak it. So...I had to go home and video tape our little guy going through his day -- following directives...such as "open the drawer and get out your swim suit" and..."go get "The Cat in the Hat" (which he successfully retrieved from a box of books and toys - that book being on the very bottom -- anyway, we called another IEP, and we had to prove that he did indeed understand language...so finally we got him into speech therapy at school for 1 hour a week (and that got bumped up to 1 1/2 hours this past semester). However, the speech therapy wasn't so much geared for producing speech -- it was more like showing 3 different items and having him select the right one, or rolling a ball back and forth to show him that in conversation we take turns (well, doesn't one have to be able to speech before they have conversation???) So...anyway, IEP #3 we proposed that producing 20 spoken words (or word approximations) actually be put on the IEP -- we actually had an IEP meeting that stretched out for 3 1/2 weeks, because I wasn't budging, and they didn't want to put that on there. But we brought in documentation from his Epileptologist and other specialists...and finally got it on there, so that speech therapy at school was actually focused on producing speech.

We did also take him to outside speech therapy, and using music and motion seemed to help in the beginning, but then for some reason his therapist abandoned that tactic, and seemed to spend 25 minutes of his 30 minute therapy sessions in behavior management (making him sit in his chair, waiting for him to comply with a directive, etc.).

Beth Israel hospital/Harvard U has been doing some ground breaking research into getting older autistic kids (older than 5) to speak again using tuned drums and the child hits the drums while the words are chanted...anyway, they have had success with their initial small trial in eliciting a few spoken words from children who have never ever spoken anything. In our case, our child has spoken before (in sentences) and has never lost his understanding of language...so I think that with the CORRECT therapy...we can hear him speak again.
 
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