European CMT Federation

A voluntary federation of all European national organizations supporting people affected by Charcot-Marie-Tooth disease.

We will:

  • Promote communication and collaboration between CMT organizations/charities.
  • Work together to fund research projects that are beyond the scope of the individual organizations.
  • Work together to advocate for greater CMT research funding from organizations such as the National Institutes of Health in the United States, European Union and the Muscular Dystrophy Associations/charities worldwide.