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?

13 comments:

msoria said...

Hello there.
My twin sister just got diagnosed with Chiari Malformation, she has had headaches for years and now we finally know why ....could you please let me know who is the doctor that did your decompression surgery? how did you find him/her? did you check references? etc, etc.
Thanks!
--Mercedes

msoria said...

Hello there.
My twin sister just got diagnosed with Chiari Malformation, she has had headaches for years and now we finally know why ....could you please let me know who is the doctor that did your decompression surgery? how did you find him/her? did you check references? etc, etc.
Thanks!
--Mercedes

offshore said...

http://www.chiarisupport.org has all the info as well as support of chiari malformation.

Anonymous said...

HI..i was diagnosed with chiari malformation of 7 mm below the magnum...is that bad?

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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.