Hi! My son is 15 and severely autistic. In the last year, he has developed epilepsy, though his seizures are not regular. He had a few absences at the beginning of last year, and then one GM, then nothing till august, and he was having 2 fits a day, until about november, and we have had nothing since(touch wood!). The neurologist we saw put him on sodium valporate, but because of the side effects we were told of, we decided to wait till after Christmas. However, I am now hesitant to start him on it at all. Maybe he won't have another fit for ages, so what is the point in giving him medication for something so infrequent.Any advice or empathy would be greatly appreciated!
And another thing that got up my nose was the neurologist putting it all down to his autism, when the two are not linked at all! Help!
Melx