I used to have a real block against connecting with people that had Epilepsy especially on forums which seemed to be the only method of connection. I didn’t want to be associated with it at all and certainly didn’t want to talk with anyone that had it for some reason. Twenty five years ago when I was diagnosed and to this day as well, there were/are no real time support groups in the city where I live that run on a weekly basis so that people can have a face to face chinwag about the fun, the freaky and the …
