Chiari Online Support Group

Hello to my fellow Chiarians!


#1

My name is Colleen. I’m a recent transplant to rural Maine. I’ve had Chiari symptoms since '07 and got a final dx in '09. Ive had decompression surgery. Crainiectomy and C1 lamenectomy. Still very symptomatic, and getting slowly worse. I’m 44. I’m having 2 MRIS next week. We shall see what they have to say, but we can all guess, can’t we? Ah well…so how’s everyone else out there in Chiariland?


#2

Hello Colleen!
I’m new to the site. I was wondering how your MRIs turned out. Did you get any answers?
Take care,
Stout