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I Think My Husband Could Benefit From A Support Group After Years Of Dealing With My Seizures. He Won't Even Consider It.
I have tried many times to tell him how much this group helps me with my seizures. You don't have to even say anything. Just read what others are going through. I wanted to know if there is a separate group of people that deal with the care of a person who epilepsy. I think he is afraid to write on the one I have because he feels I might see it. I told him you don't have to use your real name or show your picture. He always says no
My husband supports me ! I stay quiet a lot because he is overworked ! Important matters we discuss! I give you a hug!
Great to see true love their๐! Also, you can contact the Epilepsy foundation. They may be able to help you with that allowing him at his own will. Allowing it since it does have to you and life with epilepsy.
There are many families and friends of someone with Epilepsy . They all want to learn and understand epilepsy better
It is really like an advice from other people who have it a can tell you the best way to help you get around or advice for coping with it an stress
I feel that way about my son. He was 15 years old when I had my first 1. Now he 22 and still my caregiver the only thing I want him to have life outside of my health and he want
Has Anyone Else Experienced Family And Friends In Denial About Your Epilepsy Diagnoses?
Are Your Seizures Affecting Your Relationship
Can Others Who Do Not Have Epilepsy Really Help And Understand?
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