The Key Role CMT Patients Play in Research

Presented by: Joy Aldrich, HNF GRIN Patient Registry Coordinator
Without your participation, researchers won’t have the essential patient information to develop drugs, gene therapies, and clinical trials for Charcot-Marie-Tooth and other Inherited Neuropathies. In addition, as GRIN grows, we gain greater insights from you as patients to help accelerate therapies for Charcot-Marie-Tooth (CMT) and Inherited Neuropathies.

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Hello. I’m very interested in contributing with my new diagnosis of CMT. I can’t find the application. Can you tell me where can I find it? Is it HNF GRaiN? Thank you 🙏🏼