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Hello, I as diagnosed with CMT in 1992 and shortly afterward found out

that many members of my extended family that I did not know at the time

are also affected by this disease. I am a registered nurse, but have

now been on disability for 6 yrs. So far in my immediate family my

sister and my mom are the only other ones to be diagnosed, although

many of my first cousins have it. The neuropathy continues to get worse

as does the weakness, especially in the legs and fingers. I was glad to

find this website to be able to find new info and to see how other

people with CMT are affected. Sometimes I feel like no one really

understands the fatigue that we often face. Some days my legs feel as

if they just won't go. My mom and sister describe the same feeling.

Looking forward to hearing from some of you. Also, has any of you ever

heard of or experienced any problems with bowel control related to CMT?

One of my cousins thinks it may, but I never recall reading about that

problem. I think she may have something unrelated to CMT but I don't

know what.

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