Parent Project Muscular Dystrophy fights to end Duchenne. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.
Parent Project Muscular Dystrophy fights to end Duchenne. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.
If you have Duchenne or Becker muscular dystrophy or if you are a female carrier of Duchenne or Becker, join The Duchenne Registry and your data will help fuel the fight to end Duchenne. Your anonymous Registry data is shared with researchers to speed the development of new therapies.
Join The RegistryThis September, join PPMD and college football teams as we partner to raise money and awareness through Coach to Cure MD.
Help us Tackle Duchenne
Duchenne Action Month is the perfect opportunity for you, your family, your colleagues, and your community to take simple and powerful actions to raise awareness and fund the fight to End Duchenne.
Get Involved
Every single person living with Duchenne deserves the best care possible. PPMD’s Certified Duchenne Care Center Program helps to ensure that centers comply with the standards of care and services for Duchenne.
Find a Care Center
During this unprecedented time, keeping up with the latest news from federal and local governments is overwhelming. PPMD is here to help you navigate this uncertainty. Visit our COVID-19 Information Center to stay on top of the latest information regarding COVID-19 and precautions you should take if you have Duchenne.
Read the latest
The Power of Us is stronger than any one person alone. Donate now to help PPMD create innovation and support the Wellstone Muscular Dystrophy Cooperative Research Centers.
Make your donation before midnight on 12/31 and join the Power of Us.
