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Living with CMT survey

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Sorry if this has already been posted. I just took a new survey

called " Living with Charcot-Marie-Tooth " . It is located on the

Hereditary Neuropathy Foundation website at the following URL:

http://www.hereditaryneuropathy.org/clinical.html. The link is at

the very top of the page.

They were interesting, thoughtful questions. Give yourself a half

hour to take it.

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