Bernadette
An Upcoming Documentary about Living with CMT
Charcot Marie Tooth Disease - CMT Disease - Hereditary Neuropathy
THE FOUNDATION TO SUPPORT THOSE LIVING WITH CMT (CHARCOT-MARIE-TOOTH)
"This year, tens of thousands of children will sit on the sidelines because they have CMT. Please join me in supporting HNF and getting them back in the game."
Susan Lucci
Susan Lucci
Arlene has Plans... Big Plans!
Read all about Arlene in Arlene on the Scene... available in September
MEMBER LOGIN
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
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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Research
HNF develops TRIAD Program
Encourages cutting-edge research and addresses needs of CMT people.
read more...
Articles
Profiles in Courage: HNF Member John White
By John White
On July 31, 2010, I joined the HNF Spinathon by riding 50 miles on my road bike on a bike trail outside of Washington, D.C.... Read more
Coping with CMT... How to reach those 10,000 steps!
By Allison T. Moore
At least 2.6 million people are affected by CMT... Read more
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Foundation News
ARLENE ON THE SCENE Teacher's Guide Available for Download!
Hi all Arlene's friends out there, Grace's Courage Crusade is now offering a free, comprehensive Teacher's Guide for using Arlene on the Scene in the classroom.
HNF Membership Survery
Dear Friends of HNF,
HNF invites you to participate in our first ever HNF membership survey.
HNF Hamptons Spin raises $80,000 to find a cure for CMT!!!
HNF sends a very special thank you to the 70 spinners who rode their hearts out for two hours on July 31st in the beautiful Hamptons.