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.
JoinDuring 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 (Coronavirus) 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
Even though we’re apart, our community has never felt more together! Run (or walk, or roll) as one, by participating in PPMD’s first ever Race to End Duchenne Virtual Series, October 17 - November 1.
Join the Virtual Race
Let's #TackleDuchenne on Saturday, November 14! Season 12 of Coach To Cure MD is underway. Be part of the action this fall!
Get in the game
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
In response to the pandemic, Parent Project Muscular Dystrophy continues to provide resources and information about COVID-19 as it relates to Duchenne. But our work goes beyond this virus – we have a mission to fulfill and a momentum that we must maintain. Now is the time to support PPMD. Make your gift today.
