The PPMD Community Resource Center is meant to be a one-stop resource for every child, adult, and family living with Duchenne. Here you can find some of the favorite resources, products, and organizations of our community members.

As a community resource, we need your help to develop this center in order to most effectively reflect your needs.

To add to or update an existing resource, email your suggestions to resources@parentprojectmd.org.

While Parent Project Muscular Dystrophy (PPMD) strives to make the information on this website as timely and accurate as possible, PPMD makes no claims, promises, or guarantees about the accuracy, completeness, or adequacy of the contents of this site, and expressly disclaims liability for errors and omissions in the contents of this site. Reference in this site does not constitute endorsement or recommendation by PPMD. Click here to review PPMD’s policy on corporate support.

We need your help identifying state specific resources for your state. You will notice that many topics in each state are not fully fleshed out with resources, please share with us your thoughts on what resources in your state are most helpful.

Email resources@parentprojectmd.org with your suggestions.