Study Shows Sustained Benefits of PXT3003 for Patients with Charcot-Marie-Tooth Disease Type 1A (‘CMT1A’)
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Meet HNF’s Newest International Board Member, Natalia Salejko
Natalia, her family, and her growing team are laser-focused on finding a cure for CMT through aggressive fundraising through many channels.
Natural History Study Assessment of CMT patients to Support Virtual Clinical Studies
The goal of the project is to evaluate years of collected patient-reported data and to correlate the findings to specific cohorts to include genotype, phenotype and clinical features.
The Hereditary Neuropathy Foundation is excited to announce the Movement is Medicine™ Fitness Ambassador program!
We are excited to announce the launch of the Movement is Medicine™ Fitness Ambassador program, which will provide members weekly live classes that help increase their strength, balance, and overall fitness level.
Cannabis & CBD for CMT
Join our experts, Meg D’Elia & Brian Piper, PhD along with CMT patient panelists as they provide research, insight and personal experience on the topic of medical marijuana.
SORD: A Lesson in Repurposing Drugs to Treat Hereditary Neuropathy
Research from a mutation on the SORD gene
TRPV4 Hereditary Neuropathy Patients Connect with Johns Hopkins Experts to Push Research Efforts Forward
Community connected with the TRPV4 HN team at Johns Hopkins
CMT1A Clinical Trial Update: Pharnext PREMIER trial of PXT3003
The PREMIER Trial, which is being conducted in patients with mild-to-moderate CMT1A, is expected to enroll approximately 350 subjects ages 16-65 with a confirmed genetic diagnosis of CMT1A.
Rare Disease Day “Living with CMT” 2022 Art Competition
Faces of CMT Photography Contest that represents challenges living with CMT and strategies to overcome them
Brace Yourself For Another Day
Ginnell McDonald interview on writing Brace Yourself For Another Day
HNF Launches NEW Virtual CMT Fitness Platform with Ambassador Instructors
Meet Marc Daigle, Christine Panico, Julie Stone who offer live classes
Mouse Models of Human CNTNAP1 Mutations: Strategies to Rescue and Restore Functions
Research with the Department of Cellular and Integrative Physiology UT Health San Antonio, TX
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