Charcot-Marie-Tooth disease (CMT) is one of the most common inherited nerve disorders.
Read about CMT updates and the latest in CMT research. Access our archives since 2014.
Why should you join GRIN?It’s pretty simple…We need YOU!
Mitochondria is the powerhouse of our cells.
Mitochondrial is linked to some CMT subtypes.
Meet the families who are fundraising for Mito research.
Therapeutic Research In Accelerated Discovery TRIAD = Academia + Government + Industry
1 in 4,000 children are born with mitochondrial disorders.
Providing real-world data to the FDA
Part of HNF's mission is to advance and support clinical research and trials for CMT.
HNF has been conducting patient-focused research dating back to 2007.
Built to get you more shares and more followers.
Wish there was an easy guide for genetic testing? Now there is!
The program offers adaptive free online classes for everyone!
Thank you to the many faces and families who have chosen to share their stories and fundraise for their rare subtype of CMT.
Providing access to conduct Clinical Trials.
HNF has a national network designating medical Centers of Excellence (COE) for the hereditary neuropathy patient community.
HNF Board of Directors, Staff and the TRIAD Council.
We rely on your donations as we advance our mission to deliver results to our CMT family community.
Join the movement to make a difference for those living with Charcot-MarieTooth (CMT).
HNF is a 501(c) 3 public charity enabling donors to support our mission safely. There are many ways to give.
Ultimate wishlist of CMT-friendly products on Amazon to make life with CMT easier.
Donate While You Shop & Support CMT Awareness!
Join the Global Registry for Inherited Neuropathies (GRIN) and help develop drugs, gene therapies, and clinical trials for CMT and other Inherited Neuropathies! We need YOU!
Create a Facebook Fundraiser to help raise funds for CMT research.Make sure to choose, “Hereditary Neuropathy Foundation” as your non-profit.
Start a CMT Birthday Fundraiser! It's a super easy and great way to spread awareness and support CMT Research. Share to your page and let others know what CMT research means to you!
Participate in an HNF-hosted event or create your own. It’s a unique opportunity for our community to come together and celebrate and raise awareness and funds for CMT research.
Make a donation to the Hereditary Neuropathy Foundation to help find treatments and cures for those living with Charcot-Marie-Tooth and Inherited Neuropathies. We are grateful for your generosity in supporting our mission!
Questions? Email [email protected]