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Resources you can access on CMT

Because this is an archive and websites and contacts change, I'll suggest you Google CMT and you'll find all kinds of information plus organizations all over the world working with people who have CMT. Use the words CMT, Charcot-Marie-Tooth disease, hereditary motor and sensory neuropathy, HMSN, peroneal muscular atrophy, peripheral  neuropathy, muscular atrophy and hereditary neuropathy to search. It is also listed under the Muscular Dystrophy Association umbrella although it is a muscular atrophy.