I knew the only way I was going to have a fighting chance against this still unknown disease was to give CMT a voice.
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Muscle Matters: Exercise And Charcot-Marie-Tooth Disease
Exercise has the potential to improve functional ability, independence, and quality-of-life for CMT patients.
A Bi-Directional, Translational Model of Resistance-Type Exercise Training in the Management of Charcot-Marie-Tooth (CMT) Disease
A team of government researchers, including Dr. Robert Chetlin, have collaborated with Dr. Michael Sereda and Dr. Klaus Nave of the Max Planck Institute for Experimental Medicine (MPI) to successfully secure the CMT1A transgenic rat from MPI and establish a colony in the United States.
What It’s Like To Live With Charcot-Marie-Tooth Disease: The Stories Of Those Who Know It Best
The study is a collection of over 80 intimate and candid interviews, painting a vivid picture of those living with CMT. These interviews brought to light a range of different experiences: from devastating and heart-wrenching, to courageous and inspiring.
Lend A Helping Hand: Join Our #ShowYourHandsCMT Social Media Campaign!
The Hereditary Neuropathy Foundation is continuing their popular Text2Give campaign this year with the theme “Show Your Hands.”
Global Registry For Inherited Neuropathies: The Quest For A Genetic Diagnosis
The Hereditary Neuropathy Foundation (HNF) and Hannah’s Hope Fund (HHF) have partnered together to create the Global Registry For Inherited Neuropathies (GRIN).
Chrome Diva’s First Annual Motorcycle Scavenger Hunt
On Saturday July 25, 2015, Debi and Tom Houliares hosted the first annual Chrome Diva’s Motorcycle Scavenger Hunt in Webster, New York to raise awareness and funds for CMT Type 6.
Nominate yourself or a loved one as a CMT Warrior!
HNF has featured a “CMT Weekly Warrior” for the past few months on our social media platforms. This has consisted of a photo and summary to celebrate the brave individuals living with CMT.
Update on Michael Watkins – Team CMT Member
Michael Watkins completed the Leadville Trail 100 MTB race on August 15, 2015 in Leadville, CO. The trail race is widely considered one of the toughest mountain biking races in the country.
September is Charcot-Marie-Tooth (CMT) Awareness Month
In September, HNF has many ways to participate in our ongoing efforts to find a cure for CMT. Here are a few exciting and fun ways for you to join us in our efforts to raise awareness and funds
HNF Sponsors 2015 Peripheral Nerve Society Conference in Canada
Allison Moore, HNF CEO, and Joy Aldrich, HNF Advocacy Director, represented HNF as sponsors at this important conference, which was held in Chateau Mont Sainte Anne, Canada, from June 27 – July 2
Introducting HNF’s Health Care Providers Directory
The Hereditary Neuropathy Foundation (HNF) has a new initiative aimed at identifying expert Health Care Providers (HCP) for the CharcotMarie-Tooth (CMT) community.
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