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I have CMT, a genetic peripheral nerve disease.

Currently,  there is no cure for CMT. Without research we have no hope to improve our quality of life without painful surgeries, debilitating drugs for pain, annoying AFOs, hearing aids and many more temporary helps.

I am one of nine children, with a mother who had CMT. Many of us have CMT1B, as well as our children. WE NEED A CURE.  WE NEED HELP. WE NEED MONEY FOR RESEARCH. With your support today, a cure is possible. Please give today, during September CMT awareness month.

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