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I'm a new member to and wanted to take a minute to introduce

myself. My name is , I am 26 and I have CMT (sounds like AA -

huh?). Just a little humor. Anyhow, I have a 5 month old daughter

and a very understanding husband. I come from a long line of

CMTer's. Starting as early back as my great-great-Grandfather - not

that they knew it was CMT back then. It is a prevalent disease in my

family and I was diagnosed at a young age (by symptoms - did not have

DNA testing back then). Since my pregnancy my progression has

increased tremendously. Until now I've never received treatment for

the CMT because it has been livable (not enjoyable, but no surprising

symptoms since most of my family has it). Now I am in the process of

TRYING to get proper treatment. I say trying in that fashion because

as I'm sure most of you know it can be difficult dealing with doctors

and CMT. Now that I have an infant that needs constant care I don't

have a choice but to get help with this condition. And thanks to

groups like this I am receiving tons of information that is very

helpful.

Gretchen, I want to thank you for all you do for this group. I've

been reading the posts for the past week - just now had the time to

post, and the information you provide is incredible. How do you find

the time for all your research? If you lived in Colorado I would

drag you along to my doctor appts. :)

Take care,

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