More Magazine features story on Charcot-Marie-Tooth
January 27, 2012
A recent article in More magazine featured the story of Hereditary Neuropathy Foundation president Allison Moore and her experiences living with Charcot-Marie-Tooth.
The latest from HNF: research updates, patient stories, advocacy wins, events, and CMT community news.
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January 27, 2012
A recent article in More magazine featured the story of Hereditary Neuropathy Foundation president Allison Moore and her experiences living with Charcot-Marie-Tooth.
January 17, 2012
OT’s can help find holistic therapies and will collaborate with healthcare professionals to facilitate treatment.
December 15, 2011
NBC10 in Philadelphia featured a story on Bernadette Scarduzio, one of HNF's most prominent partners who is the subject of an upcoming documentary, Bernadette.
December 6, 2011
We are currently funding two very important research projects, one for CMT type 1 and the other for CMT type 2A.
November 30, 2011
The American College of Sports Medicine hosted the First World Congress for the “Exercise Is Medicine” (EIM) initiative in Baltimore, Maryland. The EIM enterprise is dedicated to improving health, wellness, and quality-of-life through regular physical activity and healthy behaviors.
November 30, 2011
Children with CMT should be active for a variety of reasons. Learn more about the benefits of exercise for kids.
November 30, 2011
Strong advocacy for education is often needed to ensure your child receives appropriate accommodations and services for academic success.
November 28, 2011
This CMT patient has worked with thousands of CMT families and draws her knowledge from past and present experiences.
November 21, 2011
New York state legislature passed a resolution memorializing NY Governor Andrew Cuomo to declare this September as CMT Awareness month in the state of New York.
November 17, 2011
"America's Friendliest Marathon," held in Richmond, VA this past weekend, included some important friends of the Hereditary Neuropathy Foundation who ran to raise awareness of Charcot-Marie-Tooth and to generate funds for research to find a cure.
September 28, 2011
Tuesday, September 27th was a beautiful evening where the New York State Podiatric Medical Association joined the Hereditary Neuropathy Foundation in celebration of Charcot-Marie-Tooth Awareness Month.
September 17, 2011
Hereditary Neuropathy Foundation sponsored a course on CMT as part of the annual meeting of the American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM).
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