We want our CMT viewers and listeners to feel like they can relate to us, and that it’s perfectly okay to be imperfect!
In 1998 Dr. Florian Thomas met a five-generation family with hereditary neuropathy leading to a research effort now entering its third decade.
HNF breaking ground with exciting gait study utilizing new digital technology – ProtoKinetics Zeno Walkway Gait Analysis System
I felt like “The Little Engine That Could.” I decided that day that CMT does not define me, it’s just a part of me. Read Gabrielle’s inspiring story here!
The CMT&ME app has updated the research app to include a brand new medical profile.
C12orf65 gene, a rare form of CMT also known as Leigh Syndrome is robbing young children of a normal life even beyond the classic CMT symptoms.
Learn the top 15 ways the Hereditary Neuropathy Foundation put your generous donations to work for you this year.
Now thanks to Marvin, my Canine Companions for IndependenceⓇ service dog, my life is so much fuller.
There’s been little research to date into how CMT affects the lives of patients…
Where do the top CMT researchers in the world unite to share leading-edge research? The Peripheral Nerve Society (PNS) meeting!
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