HACKENSACK, N.J., March 10, 2020 /PRNewswire/ -- Parent Project Muscular Dystrophy (PPMD), a nonprofit organization leading the fight to end Duchenne muscular dystrophy (Duchenne), heads to Washington, D.C., March 8–10, for their annual Advocacy Conference. Over 100 families are expected to join PPMD on Capitol Hill to help inform Members of Congress about the critical need to continue investing federal resources in Duchenne specific priorities and programs and to garner support on the recently introduced BENEFIT Act.
PPMD's Founding President and CEO, Pat Furlong, credits the success of the organization's advocacy program with the families that attend the annual meeting in Washington: "PPMD has been advocating in Washington D.C. for close to two decades. Duchenne families have been able to change the landscape of Duchenne care and research because of their consistent, unwavering advocacy efforts and an ability to build relationships with members of Congress. By sharing their stories, their personal experience with Duchenne, lawmakers better understand the importance of federal support in the fight to end Duchenne."
As they do every year, the advocates will be stressing the importance of supporting federal funding for research and essential programs. This year's request focuses on:
In addition, the advocates will ask Members of Congress for their support of S. 3385 the Better Empowerment Now to Enhance Framework and Improve Treatments (BENEFIT) Act, recently re-introduced by Senator Roger Wicker (R-MS) and Senator Amy Klobuchar (D-MN). This legislation builds on the Food and Drug Administration (FDA)'s implementation of Patient Focused-Drug Development (PFDD) provisions from the Food and Drug Administration Safety and Innovation Act (FDASIA) and the 21st Century Cures Act by requiring that FDA include PFDD data in its benefit-risk assessment for evaluating new drugs.
"PPMD has long advocated for the incorporation of patient and caregiver perspectives in regulatory decision making and therapy development. We are now in a new era of patient engagement in drug development and we believe the BENEFIT Act will send an important signal to all stakeholders that patient experience data and PFDD data will be fully incorporated into the agency's review process," said Ryan Fischer, PPMD's SVP of Community Engagement.
About the Advocacy Conference
On Sunday, March 8, advocates received extensive training and support so that they feel empowered and prepared as they attend meetings with their Members of Congress. New families are paired with seasoned advocates and meetings are scheduled throughout the day on Monday and Tuesday.
Though registration is required for PPMD's Advocacy Conference, there is no fee to attend. To learn more, click here.
If you are unable to attend the Conference in person, you can advocate from home. Click here to sign up for PPMD's Advocacy Alerts and ensure that your voice, your story is included in PPMD's messaging to lawmakers.
About Parent Project Muscular Dystrophy
Duchenne is a fatal genetic disorder that slowly robs people of their muscle strength. Parent Project Muscular Dystrophy (PPMD) is the largest most comprehensive nonprofit organization in the United States focused on finding a cure for Duchenne—our mission is to end Duchenne.
We demand optimal care standards and strive to ensure every family has access to expert healthcare providers, cutting edge treatments, and a community of support. We invest deeply in treatments for this generation of Duchenne patients and in research that will benefit future generations. Our advocacy efforts have secured hundreds of millions of dollars in funding and won three FDA approvals.
Everything we do—and everything we have done since our founding in 1994—helps those with Duchenne live longer, stronger lives. We will not rest until we end Duchenne for every single person affected by the disease. Join our fight against Duchenne at EndDuchenne.org and follow PPMD on Facebook, Twitter, Instagram, and YouTube.
SOURCE Parent Project Muscular Dystrophy (PPMD)
