I live in Western Australia. We have support groups and others in them who we can catch up with any time we like. Funds are raised for the Epilepsy Foundations. They are all wonderful. We dont have to pay for anything involving seizures or the cause if there is one.

I have been a member of the Epilepsy Foundation, for a long time, as I have been a donor to further their research, and to help those who suffer from epilepsy. Their headquarter are in Washington D.C., but they do have an office in West Los Angeles, and another one in Orange County.
Besides working to cure epilepsy, they also provide education on epilepsy, through free workshops, as well as send kids, who suffer from this disorder, to summer camps. They hold runs and other events, to raise money for research, some taking place at the Rose Bowl stadium.
I have never had direct contact, with the foundation, however, when I graduated high school, in 1974, I received a $100 gift certificate for Sears, for a new wardrobe, for college. I have no idea as to how they got my information, but I believe that this girl, who was in my graduating class, and who I was friends with, gave them my name and information.
I donate about $300 a year, because I believe that their research will end epilepsy.

Who knew i wish it had the same the for each country

As Davis said here in Oz we have a National Foundaion and most states have associations I deal with the Queensland Association they have a Facebook page and send out information and let you know about Special events they are holding.

Yes we have the Foundation and Epilepsy Action in Oz have used them both, very helpful…