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Hi Everyone,

My name is Briget and I am 54. I have been recently diagnosed with CMT by

the Department of Neurology in Pittsburgh. Although I feel the diagnosis is

correct I have yet to find a Doctor that really knows anything about CMT.

I was put on many drugs which none helped. I had the genetic Athena

diagnostic test that cost $4,000. and didn't even find out which kind of CMT

I have.

I am totally frustrated with the neurology department and have been trying

alternative medicine which I have been getting much better results from.

I was first thought to have MS, I thought I had Lyme disease. I have extreme

fatigue and was having horrible leg cramps until i started taking

supplements.

It's nice to have found another place to share our strength , hope and pain.

Peace, Briget

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