Save the date for the 2013 Advocacy Conference, February 10-12 in Washington DC.
More details to come!
About the Advocacy Conference
The Parent Project Muscular Dystrophy (PPMD) Advocacy Conference, held in the first quarter of each year, is the only officially organized gathering on Capitol Hill for the Duchenne community. Each year, participation at the PPMD Advocacy Conference grows. Scheduled visits on Capitol Hill are arranged for all attendees, giving a face and a voice to PPMD’s advocacy agenda.
We need the support of the entire community this winter as we go to Capitol Hill to make our voices heard. Your voice is just as critical as anyone else's in the fight to end Duchenne. Whether a seasoned advocate or a family new to Duchenne, we want you to join us and tell your story to the most important policymakers in our country - people who will decide how much money our government will contribute to Duchenne research.