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Posted

Hi, I'm Bethany. I just joined this group and am looking forward to finding out

more about it. I didn't really find out I had CMT until I was 12, though we

suspected before that. (I have type 1A) It's been a pretty steady decline

since then. I'm now a sophomore in highschool, but am looking into a college

program for highschool students - I worry about the stress, and also getting

around the campus. I'm still relatively mobile, but mostly I deal with fatigue

and various pains. However, I've been doing lots of research on CMT, and even

want to go into neurology someday. (I even started a blog a couple days ago,

http://lifewithcmt.blogspot.com/)

I'm interested in hearing how other people deal with their CMT, and any

suggestions for anything.

-Bethany

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