LAKEWOOD, CA — February 1, 2024 — Cure CMD is excited to be one of the seven recipient organizations of the Muscular Dystrophy...

I am 30 and I have been living with SELENON-Related Myopathy my whole life. This rare form of muscular dystrophy has affected me in many...

On September 29, I woke up eagerly because I was going sailing with my family, and not just any kind of sailing, adaptive sailing. The...

A comprehensive list of adaptive everyday products for the congenital muscular dystrophy (CMD) community to celebrate and uplift during the

For all the unintentionally insensitive and thoughtless things people have said to me over the years, no one has ever asked me the...

Inclusive Halloween ideas for all abilities. Find adaptive costumes and safely navigate accessible trick-or-treating options with a mobility

Since 2018, members of the CMD community have attended Rare Disease Week on Capitol Hill hosted by the Rare Disease Legislative...

Congratulations to this year's Creative Contest winners! Thank you to all who entered & helped support this creative initiative. See the...

Cure CMD's Advocacy Team is beginning plans for the next Rare Disease Week on Capitol Hill, scheduled for February 25-28, 2024! The...

Continuing Cure CMD’s 2023 Your Voice Matters Initiative, Lani Knutson hosted an interactive session focused on learning how to connect...

Cure CMD is proud to be joining the 2024 TCS New York City Marathon on November 3, 2024, as an official charity partner to raise funds in...

The Muscular Dystrophy Association recently announced their 2023 Research Grants, including two awards to CMD researchers! Dr. Kevin...