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?
I’m new to the site. I was wondering how your MRIs turned out. Did you get any answers?