Resources for CMT

1-855-HELPCMT (435-7268) [email protected]

Voice of the Patient
Events
Registry
HCP Directory
Medical Professionals
Clinical Trials
Blog
Newsletter
Initiatives
Resources

About
Research
Donate
Participate

Select Page

Resources

HNF provides a wealth of resources for those living with CMT/IN.

What is CMT

What is CMT?

Events

Events

CMT Diagnosis

CMT Diagnosis

The Mighty

The Mighty

Inspire Community

Inspire Community

Advocacy

Advocacy

About HNF

Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 organization which mission is to increase awareness and accurate diagnosis of Charcot-Marie-Tooth (CMT) and related inherited neuropathies, support patients and families with critical information to improve quality of life, and fund research that will lead to treatments and cures.

Join Our Mailing List

Receive the latest news about the CMT/IN community, research, and events. We respect your privacy. Your email will not be shared.

Search Our Site

Search for:

First Name:

Last Name:

Email address:

Leave this field empty if you're human:

HOME
CONTACT US
PRIVACY POLICY
TERMS OF USE
MEDICAL DISCLOSURE

Facebook
Twitter
Youtube
Pinterest

Copyright ©2018 Hereditary Neuropathy Foundation | 401 Park Avenue South, 10th Floor NY, NY 10016 | Web Design by Footprint Digital | Web Hosting by COMMbits Inc.