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hello everyone, i have not posted in a while, but i read everything and i am

very thankful for the wealth of information that is out there.

Just a reminder about my situation, my father has had CMT for 40 years, but i

(the daughter) have shown no symptoms. CMT is very prevelent in the family and

can be traced back. My dad is an only child and I am not hopeful enough to think

that I will be spared.

I have a sister that has very mild early symptoms of sensation loss of her toes.

My question to you is this: should i get genetic testing to see if i have it? I

am not the type to freak out about every little tingle and say " uhoh here it

comes " I am just curious. I am very on the fence and just looking for feedback.

I also am concerned about the genetic discrimination bill, I do agree that

insurance companies will find a way around things. they always do. thanks for

everything

julie

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