Do You Belong To An In-person Social/support Group For Epileptics?
When I was younger I use to go to a support group thru the Epilepsy Foundation.
Today I use this site , which is a social / support group. It a much larger community. There are people from accross the world here sharing and talking about their Epilepsy. Even people who have a family member with Epilepsy are learning from us.
Look up TTWP. Turning The World Purple. Its a nonprofit epilepsy group run by someone I know name Michelle Cole Hernandez. She lives in Louisiana.
I'm in alot of chat groups. There is a weekly get together via zoom that I always get invited to but I'm still yet to do it.
I talk to some chat groups online. Thats how I met a few friends. Now we socialize privately
this is the only one.
A Neutral? Technology And How We Talk To Each Other About Our Conditions And Such Etc,we Have Quite A Site Here And Is Helpful And Useful,
I Know We Talk About Our Conditions And Such Etc Online On This Site, But Have You Met Up With In Person? Just Curious.
Where Can We Get An Epilepsy Medical To Finish It?? Because It As Destroyed My Family Any Supporting Please (Email Address Can Only Be Seen By MyEpilepsyTeam Users) ?
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