Friday, September 24, 2010

Something to Ponder

I'm thinking of doing the Chiari Walk in Colorado next year (in September)...maybe getting all of my buddies who have found me here to join me there...and see Dr. Oro. Anyone want to join me?
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My life with Chiari Malformation Type I

This is just my story of my experience with Chiari. Until I was diagnosed, I'd never heard of it, and I just want more people to be aware of it. I'm not a doctor, so don't quote me on any of this stuff - k? If you are looking for information about Chiari Malformation, a lot of the more informative posts are the older ones.