Hey there. I'm sorry the same things are going on with you, although i'm glad to have found this forum and find others. I do alot of research on the internet so I can understand it more... But i've never talked or known anyone else with it. My fiance also will be using this screen name. So on any given post it might be from me or from him.
Thanks for writing. It never even occured to me that maybe he could hear me while having a siezure. I'm curious to see.
Another thing is i've noticed there are alot of epilepsy awarness/funded programs and walks in europian countries. And none here in the usa. Since your in australia... Do you know of any around you? I try to look for anything epilepsy related, but there is nothing around here. Kind of sad.