CMT Updates
Read about CMT updates and the latest in CMT research. Access archives since 2014.
Related Blog Posts
Disease Awareness Problem
video of Robert’s keynote about CMT going largely unrecognized
Top 10 Ways to Spread CMT Awareness
HNF HAS COME UP WITH TEN WAYS YOU CAN DO YOUR PART AND HELP ALL OF US SPREAD CHARCOT-MARIE-TOOTH AWARENESS:
Thank You to Everyone Involved with PLEO-CMT Trial!
a drug candidate has reached Phase 3 clinical trial, the critical last phase before potential FDA market approval
HNPP Study Available for HNF Members
This study, which aims to uncover the rather unrecognized symptoms of Hereditary Neuropathy with Liability to Pressure Palsy (HNPP)
Patient-Centered Summit for CMT/HNPP: Cambridge, MA November 3, 2017
HNF is excited to hold the 2nd Annual Patient-Centered Summit with a focus this year on CMT/HNPP and Pain in Cambridge, MA!
10 Ways Participating In GRIN Helps Support CMT/IN Research
HNF’s Global Registry for Inherited Neuropathies (GRIN) is one of our initiatives that supports our commitment and dedication to developing treatments and discovering cures for CMT and other INs.
About The Summit Venue: 3 West Club, New York City
The Hereditary Neuropathy Foundation has selected historic 3 West Club to hold the first Patient-Centered Charcot-Marie-Tooth Summit on October 6, 2016.
Summit Speaker Spotlight: Gary Barg, The Fearless Caregiver
Those caring for patients living with CMT are invaluable members of our community. Caregivers are on the frontlines every day, helping patients manage their daily struggles and challenges of living with CMT.
Applying for Disability with Hereditary Neuropathy or CMT
Learn how you can apply for disability with Hereditary Neuropathy or CMT.
Top Ten Ways Participating in GRIN Helps Support CMT/IN Research
HNF’s Global Registry for Inherited Neuropathies (GRIN) is one of our initiatives that supports our commitment and dedication to developing treatments and discovering cures for CMT and other INs.