Emotional Affect (PSY Project)

Welcome to the Coping With Epilepsy Forums

Welcome to the Coping With Epilepsy forums - a peer support community for folks dealing (directly or indirectly) with seizure disorders. You can visit the forum page to see the list of forum nodes (categories/rooms) for topics.

Please have a look around and if you like what you see, please consider registering an account and joining the discussions. When you register an account and log in, you may enjoy additional benefits including no ads, access to members only (ie. private) forum nodes and more. Registering an account is free - you have nothing to lose!

Messages
11
Reaction score
0
Points
0
How did being diagnosed with epilepsy affect you emotionally? For me it didn't have an impact because I was so young. Of course as I got older I felt more ostracized because of my seizures but that didn't have much to do with the diagnosis itself. That was more of the way I felt because of the reactions I got. If it had been more accepted by the people around me then it would have continued to have little impact.
 
Being dx'd with epilepsy epilepsy didn't change me I was dx'd when I was two yrs old.
But as a child I heard don't play with her because of my seizures this was the 60's.
I found kids to be cruel in H.school because of my seizures I was teased often because of them. I accepted my epilepsy but ppl around me seemed to have problems if I had a seizure and adults are as bad as children. Adults get personal kids don't know better.
I live my life and if I have a seizure so be it.
 
I was dx'd when I was 16 and in high shool. Honestly, the biggest problem was not driving. Sure, that was a little tough, emotionally, but honestly, emotions weren't much of a problem. I'm sure it would be much tougher to be my age now (27) and diagnosed.

Since my seizures were at the worst complex-partial until I was 25, they were rarely noticed. Even having had a few tonic-clonic, they still don't effect me emotionally.
 
Back
Top Bottom