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My Introduction

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Hi, my name is Sunshine and my 3 year old was diagnosed last year

with CMT 1A and that's when I found out that I also have it. There's

also the possibility that my almost 5 year old has it.

It's nice to know that there are others out there that are

experiencing the same as us.

I've heard mention of the Vitamin C research and am curious to know

what it is.

I look forward to getting to know members of the community.

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