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Gwolfgarona

800d

I have not had much opportunity to talk to anyone else with CMT. I did a summer camp for Muscular Dystrophy back before CMT left that umbrella. Not any other kids there with CMT that year anyway. I want to hear other people's experiences with this disease and in turn share mine.

☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision

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