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Hi, and

welcome to CWE!

You've gotten some wonderful advice from the previous posters.

Diet is an important thing to pay attention to...so is sleep. (Watching both of those things have kept me from having too many seizures in the last few years.) Keeping track of everything to help himself and the doctors too, will help your son in the long run even if it IS a pain in the ARSE.

Being the E patient myself, I know I get ANNOYED when I have one of mine. Let your son talk about how he feels. It's an important thing. Sometimes E can be very irritating.....maddening and depressing. He can even come here and vent in the Padded Room if he wants to.

No matter what though, we will be here for you. There is no reason to be scared. And if we don't know the answers, we can probably direct you towards the right direction to get it.

Take care!

Meetz
:rock:
 
He has been seen by a neurologist. It was the neurologist that diagnosed the Epilepsy. It's weird but my son is not having a hard time adjusting to the do's and don'ts! In fact, he's being so responsible about it, I'm just amazed!
 
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