My thoughts, rants, and experiences regarding epilepsy and the stigma attached to those who have it. Seven years ago, my daughter was diagnosed with epilepsy, and it has been a wild ride. I decided my experiences and knowledge just has to be able to help someone, so here I am.
Wednesday, October 20, 2010
What I'm Doing Here
In 2004, my 16 month old baby had her first seizure. I didn't know what was happening, and though I knew basically what to do when a person is having a seizure, I was woefully unprepared for what we were about to encounter. She's had hundreds of seizures in the last six years, and I've learned to work the medical and education system. It's been an exercise in trial and error. My goal with this blog (and hopefully, eventually a web site) is to create a resource for parents/caregivers of children with epilepsy (or any special need). I'm hoping that my experiences, knowledge, and rants will be helpful to someone besides myself.
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1 comment:
Oh, dang. I just watched that video. I really want to help you help others Ms.Nave.
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