Charcot Marie Tooth Disease - CMT Disease - Hereditary Neuropathy

THE FOUNDATION TO SUPPORT THOSE LIVING WITH CMT (CHARCOT-MARIE-TOOTH)
HNF

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An Upcoming Documentary about Living with CMT

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Arlene has Plans... Big Plans!

Read all about Arlene in  Arlene on the Scene... available in September

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Hereditary Neuropathy Foundation, Inc.
1751 2nd Avenue, Suite 103, NY NY 10128
NY Tel: 212-722-8396
Toll Free: 877-463-1287
info@hnf-cure.org
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Andrew Collins, a Florida Teen Living with CMT, Tells the Story of how the Disease Impacts His Life

Issue date:  Tue, 05/27/2008 Author Name:  Andrew Collins Recently, we spoke with teenager Andrew Collins, a 14-year-old living with CMT in Longwood, Florida, with his parents and younger brother, Matt, who is 11 and ... Full text available to Members Only. Please log in at the left side of the page ...


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