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 RegistryYour gifts now go TWICE as far! Thanks to a generous family in our community, all gifts made in support of PPMD’s Dystrophinopathy Clinical Research Network will be matched up to $100,000 through midnight on 12/31!
Together, let’s advance the research evolution. Give today and DOUBLE your impact!