Yeah I found it when I was look thru all tha shit on Facebook. See your kinda like me just reading about others problems boy it's crazy and hard to believe some stuff. Everyone is not the same I just wish I could get the doctors to understand that Medicaid doctors really suck when it comes to helping people with epilepsy. It sucks I have to pay cash to get the doctors to actually help me with my problems all they want to do is Rob Medicaid. (Phone number can only be seen by the question and answer creators) Thats my number call it sometimes if I can help anytime. THANKS MY Epilepsy actually didn't start until I graduated college an was arrested for smoking pot when they made me quit smoking is when I started having my SEIZURES and it really sucks because of all the time and classes I took in college for WELDING certification an those flashing lights causes me to have SEIZURES, so then I went back and then got certification on the computers. Then they put on DISABILITY FOR THE EPILEPSY. NOT BEING ABLE TO WORK REALLY SUCKS.

I was already on another epilepsy site and this one popped up so I clicked on to check it out. I really enjoy it.

I'm forty one myself if you need to know anything about someone else's life with this crapie stuff. I need help from everyone else in trying to get a primary care physician and a neurologist an maybe even a physiological doctor. I was fine until I got on this damn Medicaid and lost my doctors an my meds. These Medicaid doctors around Birmingham don't listen all they want to do is Rob Medicaid. All I need is Dilantin and Xanax for my Epilepsy and insomnia. I wouldn't need the all the other pills. Instead of just prescribing the Xanax the doc has me taking 1dilantin, 2pika for the SEIZURES and 3transodone and 4mimitate for my insomnia and 5neuronton and 6suboxone for my Epilepsy and pain with the 7Busparone to help with my depression stress and anxiety. If a real doctor would just prescribe me 3 different meds instead of them 7 with all those different side effects are almost as bad as SEIZURES.

I was searching for a site with Epilepsy support. Unless I have someone drive me to the Epilepsy Foundation in the U.S.A. , it would be difficult to going to their support groups. I found this site , and it was easy to relate to many of the subjects people were talking about.

@A MyEpilepsyTeam Member That's great! I love reading the knowledge and experiences people have and have gone through 🙂