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Junior Member
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Hello everyone.
I am new to the site and am very happy to have found it! I have recently been diagnosed with Charot Marie Tooth Syndrome. This is a genetic neuropathy. I will be meeting with my neurologist in two weeks to discuss this diagnosis. If anyone out there has CMT, do you have any suggestions regarding what types of questions I should ask, or give me some advice on your experiences? How are you dealing with the symptoms? I would be grateful for the help. Di |
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