
For more information on H.E.L.P. Fund or to support CMT2 research, click here.
For more information on H.E.L.P. Fund or to support CMT2 research, click here.
As we start the new year energized and ready to continue our mission of bringing treatments and...
Join Iris Adler as she continues fundraising for her grandson and the many others living with Charcot-Marie-Tooth Type 2A
HNF has been committed to funding HDAC inhibitor research since 2014.
Join us on September 9th in Victor, NY for a Scavenger Hunt to help raise funds for CMT 6 research.
Join HNF at the MightyMan Half Iron Distance in Fort Pond, Montauk, NY October 1st.
HNF cast off for our maiden voyage New York City sunset cruise to raise funds for CMT research.
Join this exclusive research study for people with CMT featuring the AlterG anti-gravity treadmill.
The National Organization for Rare Diseases has awarded HNF funding to build a robust natural history study to support the second most common type of CMT called hereditary neuropathy pressure palsies (HNPP).
Q&A with Dave Washabaugh
HNF has launched a new Patient-Reported Research Study to advance therapies for CMT and inherited neuropathies (IN) in an effort to collect comprehensive data for a better understanding of the disease.
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