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What experiences do we share, and what barriers confront us? Is it possible to replace our contemporary, medicalized culture with something more representative of us as complete beings? Are we ready for a real sense of community yet? I think so.
This is a blog about epilepsy. I have lived with seizures for 23 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 2 years ago and have posted on that extensively. Please feel free to comment and I will try to respond.
I have been an epilepsy advocate for 9 years. It is extremely difficult and challenging for an individual to promote epilepsy awareness single handedly but it is not totally impossible.
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