Guest guest Posted April 25, 2006 Report Posted April 25, 2006 Whoops! I missed the boat and just got around to responding. I was going to say that I never got to see Sophia develop normally because the seizures started at 2 weeks old, but I could see how seizures and meds would dramatically change a child. I would blame the meds more, as they seem to have so many small side effects, like irritability, nausea, drowsiness, etc. Those could definitely affect a personality. As far as the seizures and damage, our neuros have told us that it's the big seizures (longer than 20 or 30 minutes) which cause damage. The small ones don't but they do affect the brain over time, which I believe means years. Seizure control seems to be a huge key to development, which I'm guessing from my other yahoo group where pretty much no one has seizure control and development is extremely limited. Anyway, hang in there and I hope feels like himself again soon! > > Thanks to C, Steve, Joanne, Sidney's mom/dad, dana & Dom for > your replies re diagnosis of your child and how they changed. I guess > it may just be that I am thinking about this all too much and miss the > old but I love my boy heaps!!!!and will do the best I can for him > even though at times I do not know what he needs really - as you guys > know only too well. > Quote
Guest guest Posted April 27, 2006 Report Posted April 27, 2006 Its never too late for a response!! How is Sophia going now? What meds is she on? > > > > Thanks to C, Steve, Joanne, Sidney's mom/dad, dana & Dom for > > your replies re diagnosis of your child and how they changed. I > guess > > it may just be that I am thinking about this all too much and miss > the > > old but I love my boy heaps!!!!and will do the best I can for > him > > even though at times I do not know what he needs really - as you > guys > > know only too well. > > > Quote
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