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Welcome , thanks for introducing yourself. Perhaps would you

share about your two mutations, since they are so close (Type 1)

As for the 'shaky' feeling - I'm not quite sure what you mean, but

this could be 'tremors'. I was already diagnosed for ten years before

I got them. Research I have done points to Roussey-Levy Syndrome

(aka, CMT with Tremors) which have been traced back to the original

family that has Type 1B.

CMT affects members of the same family differently and at differnt

degrees - perhaps this is why you see this in your son.

However, I myself, have a type of CMT 2. No CMT anywhere in my

pedigree as far back as I can get records (that was 1750!) I have

normal EMG/NCV's with reinnervation and am mildly affected. Life is

very full, stimulating, enriching, and exciting for me with work,

love, travel, regular exercising, some supplements and a very well

maintained diet including extra hydration.

I hope you'll meet many friends here and find helpful.

~ Gretchen (Founder and Moderator of )

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