CMT: Charcot-Marie-Tooth & The Hereditary Neuropathy Foundation

The Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 dedicated to finding treatments and a cure for Charcot-Marie-Tooth disease (CMT) and related peripheral neuropathies while providing support and extensive information for those living with CMT and their families.

HNF promotes and supports both clinical and primary CMT research. We are also actively committed to increasing awareness of the disease through all available media outlets, including print, radio and television as well as fundraising programs. While our members give a face to CMT, HNF provides a strong, organizational voice to those living with CMT all over the world.

HNF will continue to educate physicians, along with the entire medical community about CMT. We will also continue our pledge to become the definitive information outlet for the general public about this important, often misunderstood disease. Our innovative, highly proactive website is committed to presenting up-to-date information, resources, support, international discussion forums, Q & A's, along with numerous helpful products and services that are available to individuals living with CMT.