My rare disease advocacy journey started later in life. Like many, I had always felt too overwhelmed and unsure of how to start and was...

LAKEWOOD, CA — February 2, 2024 — Cure CMD & The Caregiver Compass team up to release a special edition caregiver guidebook for the CMD...

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

By September 30, 2023, Congress must reauthorize the Federal Aviation Act (FAA). Changes can be made when an act is reauthorized, and advoca

Many steps must be taken to ensure you get the "full college experience" that other kids get while staying on campus. Here, I will share wha

If you’re reading this, you probably already know that a key part of Cure CMD’s mission is to help support the CMD community through...

Liam Miller is a 21-year-old Computer Science major in his final year at Temple University. Like many 20-somethings, Liam lives on his...

Community member, Daniella Slon wrote this article about accessibility in her hometown. We hope this inspires you to investigate your...

Vehicles and Conversions The privilege for any disabled person is to obtain their driver's license and drive a vehicle. Driving can give...