This is a blog about epilepsy. I have lived with seizures for 25 years now and I want to share my experiences to allow others with epilepsy a chance to compare their experiences to mine and to allow those without epilepsy to understand further the condition and how it effects one. I had the VNS device implanted 4 years ago and have posted on that extensively. Please feel free to comment and I will try to respond.
Tuesday, May 02, 2006
Epilepsy Foundation - North Carolina
Today, Christa and I met with the director of the NC chapter of the Epilepsy Foundation of America. We learned all about the events that their chapter has planned this year. Their organization is primarily focused on the medicine fund for people that cannot afford anti-epileptic drugs (AEDs). We volunteered to help out with a variety of fundraising efforts, including an upcoming Chili Cook-off that will be held at the local farmer's market. If anyone is interested in the details, let me know.
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