John's condition hasn't changed in the last couple of weeks, so we are going back to see the neurologist later this week. He's doing great, but we'll keep adjusting things until he's completely seizure-free.
Yoshie took John to the morning ESD class yesterday. That turned out to be far too advanced for him. Niether of the classes he's been to have been right for him - they've either been too advanced, or too slow. There isn't a "middle" class, so Yoshie talked to the teacher about trying to get more personalized therapy. Hopefully that will work out, though it appears that it isn't that easy to just change things once the IEP is written.
So far private therapy hasn't worked out, either. We'll keep trying.
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