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CMTA News

WinterNewsletter2021


The Winter 2021 CMTA Report

Read the latest CMTA Report for updates on CMT research, community stories, an awareness month recap, CMT news, and more!

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Annual Appeal Family Picture


Keep Hope Alive for Everyone Living with CMT

Families that live with CMT all share one hope: that their children and grandchildren will grow up without the fear of CMT hanging over them.

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CMT 4 Me Podcast

CMT 4 Me is an emotional, heartfelt, and humorous podcast for the 3 million people who have Charcot-Marie-Tooth disease, friends, family, and the general public.

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Alan Jackson CMT Story


Alan Jackson shares his CMT story with the Today Show

Alan Jackson shares his journey with Charcot-Marie-Tooth disease on the Today Show with Jenna Bush Hager.

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The 2020 CMTA Annual Report

Inside: Accelerating research and empowering patients. We’re very grateful for your contributions and for your interest in what the CMTA is doing to advance research, create awareness, and make life better for everyone affected by CMT.

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CMTA Innervators


CMTA Innervators

CMTA INNERVATORS are action-oriented game-changers. They sustain the CMTA with monthly gifts throughout the year.

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What is CMT?

Living With CMT

CMT doesn’t have to stop you from doing the things you want to do. We have ...

Living with CMT

Researching the Cure

Over $17 million invested in STAR research driving our vision of a world without CMT ..

Our Research

Find a Local Branch

Find a CMTA Branch Near You

With over 70 branches across the United States and two in Canada the CMTA helps connect patients to local resources.

Get Involved

Join us as we walk to raise money for a cure.

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Walk 4 CMT

Do your part to advance possible treatments for CMT.

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Patients as Partners in Research

Make CMT and the CMTA your cause.

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Start Your "OWN" Fundraiser

The only camp in the US just for kids with CMT.

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Camp Footprint