They Rode for a Cure and you Can Still Be Part of It
May 18, 2026
News & Stories
Patient stories from the Charcot-Marie-Tooth (CMT) community: lived experience, journeys, and voices featured by the Hereditary Neuropathy Foundation.
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Showing 1 to 12 of 55 in Stories
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Passion for Movement. Power for Change.
September 18, 2025
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CMT Warriors Unite: Rock, Roll, & Make a Difference in San Antonio, TX
October 3, 2024
Event Details: San Antonio, TX: December 7-8, 2024 (5K, 10K, Half Marathon, Full Marathon)
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HNF Awards the inaugural HNF Clinical Translation Fellowship
August 16, 2024
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Unstoppable Skyler Fisher: Triumphing Across Continents with CMT
February 27, 2024
In the fast-paced world of para triathlons, one name stands out among the rest: Skyler Fisher, a dynamic 19-year-old powerhouse representing Team USA.
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TD Bank Five Boro Bike Tour
November 8, 2023
HNF is thrilled to have been chosen for the 14th year as a Charity Partner for the TD Bank Five Boro Bike Tour.
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HNF sheds Light & Research Funding on Mitochondrial Diseases Linked to CMT
June 13, 2023
Mitochondria are the powerhouses of our cells. Think of them as our body’s batteries. Mitochondrial disease causes these batteries to run low.
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CMT Safe Space - Best Shoes for High-Arched Feet?
March 21, 2023
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CMT Beyond Social Media: What is CMT Safe Space!
March 14, 2023
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Bike for CMT Research | TD Bank Five Boro Bike Tour
March 7, 2023
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The Houliares Family Takes on CMT6
March 6, 2023
We have two choices in this world. We can sit back and do nothing, allowing this disease to happen, or we can go out and fight to make a difference.
