Mary Cate, a woman wearing a helmet and a blue shirt that says “Cycle 4 CMT”, rides her bicycle down a long straight road which cuts through a beautiful lush landscape of grass and sparse trees.

Mary Cate on her Cycle 4 CMT fundraiser!

CMT4C is a severe neurological disease without a cure.

With YOUR help, we can get a viable, research-backed treatment into the hands of our loved ones. Donate today!

Aaron, Mary Cate, and Dr. Kleopas stand together holding a sign that reads "CMTA: Cycle 4 CMT". In this fundraiser, they successfully raised over twenty-three thousand dollars that will go directly towards funding a cure for CMT4C! — Aaron, Mary Cate, and Dr. Kleopas stand together holding a sign that reads "CMTA: Cycle 4 CMT". In this fundraiser, they successfully raised over $23,000 that will go directly towards funding a cure for CMT4C!

The CMT4C Advocacy Group is working to connect those affected by Charcot-Marie-Tooth disease type 4C: patients, loved ones and the organizations and researchers who are developing treatments.

CMT4C is a rare disease caused by a mutation of a gene called SH3TC2 which affects the peripheral nerves and results in progressive loss of function and sensation in the extremities, along with deformities in the spine and feet.

While there is currently no FDA approved treatments or cures for any form of CMT, there is lots of promising research on the horizon.

Our purpose is to create a community that embraces individuals impacted by CMT4C, along with their families and the professionals dedicated to supporting us, as we collectively strive towards a cure.