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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.
Whats About The Latest Researches On #refractary #epileptic Patients…and Medicines Who’s Might Been Correctly For’em
A ? Do You Think That With Our Conditions We Have Are You Ok With That And Do Feel It's A So Called Norm And Are Ok With?
Are You Willing To Do Whatever Is Necessary To Help New Members Feel Comfortable And Quickly Have A Team Of Many?
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