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 29, 2012
One Brain Fart at a Time
Copperpaws just started a new blog on living with his particular brand of epilepsy. You can check it out at: OneBrainFart.blogspot.com
http://www.gofundme.com/helpsteven
ReplyDeleteDonate to the fund I created for my brother battling Epilepsy!
Thank you!
Good luck Lexie!
ReplyDeleteKeep trucking on mate!
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