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)
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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PLANNING AN HNF EVENT/CAMPAIGN
Host an HNF event in your hometown! Reach out to friends, family, and business associates to help raise funds for HNF. The HNF staff will assist you in your fundraising efforts by creating a website, marketing, and sending a representative for the day of the event.
Spin-a-Thon:
Host a spin-a-thon at your local gym. It’s easy, fun, and healthy!
Golf Event:
If you are a golfer, you can hit the links and raise funds to cure CMT.
Cocktail Party:
Invite your closest friends, family, and business associates interested in philanthropy to a party to raise funds for HNF.
Friends & Family Letter:
Don’t have time to host an event? Send a letter to your friends and family to help them understand the devastating effects of CMT. HNF can assist in writing the letter and will supply any of our publications to send along with it.