Urge your House and Senate Members to Support the FY 2023 Duchenne Funding Request & BENEFIT Act
It’s that time of year again. Members of the House and Senate are working, right now, to develop and submit their policy priorities for the annual spending bills that will fund the NIH, CDC, DOD, FDA, and other key federal agencies for 2023.
We need you to contact your House and Senate members as soon as possible and urge them to continue making Duchenne patient care, public health, and research a top priority. Click here to learn more about this year’s request to Congress.
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Support the FY 2023 Duchenne Appropriations Request and the BENEFIT Act
Dear [Decision Maker],
In 2001 Congress enacted the Muscular Dystrophy Community Assistance, Research and Education or MD CARE Act, which dramatically transformed efforts to combat Duchenne and other forms of Muscular Dystrophy. As a result of this Act and subsequent amendments, federal commitments to research expanded, helping spur scientific breakthroughs to develop potential therapies. These commitments have also leveraged significant non-federal funding from academic institutions, industry, and venture investors in a true public-private partnership model. In addition to research breakthroughs, the MD CARE Act has helped standardize patient care. These care standards have helped markedly lengthen and improve the lifespan of the average Duchenne patient.Achieving future success requires the continued support of programs and policies to support Duchenne research, public health and drug development efforts. We need your help. To support this work, our first request is for you to please sign onto the annual Duchenne appropriations sign-on letter being led by Senators Roger Wicker (R-MS) and Debbie Stabenow (D-MI) in the Senate and Congresswoman Doris Matsui (D-CA) and Congressman Troy Balderson (R-OH) in the House. This letter seeks support for key Duchenne programs and policies including: $8 million for CDC's Muscular Dystrophy Program funding $12 million for the Duchenne Muscular Dystrophy Research Program within DOD's Congressionally Directed Medical Research Programs (CDMRP) Update the Care Considerations to reflect approved therapies, and advancements in care realted to cardiac and mental health. Support research at NIH on challenges related to gene therapies and ask FDA to enable the development pathway of genetic therapies across the spectrum, particularly those that lack the patient population to incentivize drug developers.I urge you to sign onto the FY23 letter which means so much to me and my family. For questions on the Senate letter, please contact either Kirby Miller (Kirby_miller@wicker.senate.gov) with Senator Wicker or Sarah Jamgotch (Sarah_Jamgotch@stabenow.senate.gov) with Senator Stabenow. To sign the House letter, please contact Christina McCauley (firstname.lastname@example.org) with Rep. Matsui or Davis Michols (email@example.com) with Rep. Balderson.
Sincerely,[Your Name] [Your Address] [City, State ZIP][Your Email]