The Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)(3) organization which raises awareness, funds scientific research, and educates the medical community as well as the general public about Charcot-Marie-Tooth disease (CMT). HNF is committed to providing support to people living with CMT and their families.
You can contribute by joining Team CMT or with the options below!
Race For Research
You may be wondering what you can do to help
Raising Funds For Awareness in NYC
Running and participating in athletic events is what most people with CMT only dream about. For many of them, even the simplest activities of daily life can be challenging, but we all share the dream of being able to walk, run and do all the things others do with ease. In 2012, 2013, and 2014 I ran the Boston Marathon to raise awareness for CMT and to raise funds for CMT programs and research. In 2018 I will be running the New York Marathon. My fund raising goal is $10,000 Click the button below to if you’d like to contribute to my efforts!
RUNNING FOR MY LIFE
WINNING FOR CMT
I know I am lucky to be so active when many with this condition struggle to do everyday tasks. Like my Team CMT teammates, I swim, bike and run for those who can’t. I hope you will continue to support our mission to find treatments and a cure!I wrote a book about my CMT journey. With every book that is purchased, $5 goes to HNF.Buy Now!
A Journey Toward Healthy Living
A delicious and healthy collection of soup recipes by triathlete and long-distance runner Christine Wodke.Download Now!