"Hello Paige! I love that name its my daughters name also. I also have the vns. I know it probably hurts bad right now. But it will get better. I had mine put in dec 2012. No seizures thus far. So good luck to ya dear! Purple power!"
"Hi Paige my name is Cody I also have VNS I have been doing pretty good with it. Ive had it for three years now and my seizures have decreased a whole lot. Im really thankful for the doctors that did this for me and im thankful to God for putting…"
Welcome to the site. It's a great place to be. We're happy to have you here, and if there's anything I can do for you, please don't hesitate to ask.
I also wanted to let you know about two groups I created.Living Well…"
Welcome to the site. I am sure you will find our site warm and friendly. Feel free to browse my blog if you wish and ask me any questions you may have. I'm more than happy to help.
"Hello, this is Gigi an Information Specialist with the Epilepsy Resource Center. Welcome to ecommunities. The Epilepsy Resource Center provides information about epilepsy, community referral information for support and…"
Hello, this is Gigi an Information Specialist with the Epilepsy Resource Center. Welcome to ecommunities. The Epilepsy Resource Center provides information about epilepsy, community referral information for support and assistance, and literature resources to increase understanding of the condition and improve management of the condition. Please feel free to contact the Epilepsy Resource Center Monday through Friday 9am-5pm (Eastern Standard Time) for specific information or referral services @ 1/800/332-1000.
Also, check out the latest Epilepsy Foundation community outreach programs: