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Bill > S315
US S315
US S315Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education (MD-CARE) Amendments of 2013
summary
Introduced
02/13/2013
02/13/2013
In Committee
07/23/2014
07/23/2014
Crossed Over
Passed
Dead
01/03/2015
01/03/2015
Introduced Session
113th Congress
Bill Summary
Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education (MD-CARE) Amendments of 2013 - Amends the Public Health Service Act to revise the muscular dystrophy research program of the National Institutes of Health (NIH). Multiplies the forms of muscular dystrophy included within the program. Requires the research conducted through Paul D. Wellstone Muscular Dystrophy Cooperative Research Centers to include cardiac and pulmonary function research. Requires the Director of NIH to ensure the sharing of data between such centers. Revises the composition of the Muscular Dystrophy Coordinating Committee (MDCC) to include the Social Security Administration and the United States Administration for Community Living. Requires the MDCC to meet at least two times per year. Requires the MDCC Action Plan to provide for: (1) health economic studies to demonstrate the cost-effectiveness of providing independent living resources and support to patients with various forms of muscular dystrophy, (2) studies to determine optimal clinical care interventions for adults with various forms of muscular dystrophy, and (3) the development of clinical interventions to improve the health of adults with various forms of muscular dystrophy. Requires the MDCC to develop a plan to expedite the evaluation and approval of emerging therapies and personalized medicines that have the potential to decrease fatal disease progression across the various forms of muscular dystrophy. Requires the Secretary of Health and Human Services (HHS), in carrying out epidemiological activities regarding Duchenne and other forms of muscular dystrophies, to ensure that data from different racial and ethnic populations is captured and made publicly available to investigators conducting public or private research on muscular dystrophy. Directs the Secretary to foster ongoing engagement and collaboration between the surveillance program and the research centers. Amends the Muscular Dystrophy Community Assistance, Research, and Education Amendments of 2001 to authorize the Secretary to: (1) update and disseminate widely existing Duchenne-Becker muscular dystrophy care considerations for pediatric patients, and (2) develop and disseminate widely Duchenne-Becker muscular dystrophy considerations for adult patients and acute care considerations for all muscular dystrophy populations. Directs that such care considerations should build upon existing efforts currently underway for specified forms of muscular dystrophy and incorporate strategies specifically responding to the findings of the national transitions survey of minority, young adult, and adult communities of muscular dystrophy patients.
AI Summary
This bill, the Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education (MD-CARE) Amendments of 2013, aims to enhance research and support for individuals with muscular dystrophy by expanding the types of muscular dystrophy studied by the National Institutes of Health (NIH), ensuring that research conducted at the Paul D. Wellstone Muscular Dystrophy Cooperative Research Centers includes studies on cardiac and pulmonary function, and mandating the sharing of data between these centers. It also broadens the membership of the Muscular Dystrophy Coordinating Committee (MDCC) to include the Social Security Administration and the United States Administration for Community Living, requiring the MDCC to meet at least twice annually and to develop an action plan that includes health economic studies on independent living resources, optimal clinical care interventions for adults, and strategies to expedite the evaluation and approval of emerging therapies. Furthermore, the bill requires the Secretary of Health and Human Services to ensure that epidemiological data on muscular dystrophy, particularly Duchenne and Becker forms, captures diverse racial and ethnic populations and is publicly available, while also fostering collaboration between surveillance programs and research centers. Finally, it directs the Secretary to update and disseminate care guidelines for Duchenne-Becker muscular dystrophy for both pediatric and adult patients, as well as acute care considerations for all muscular dystrophy populations, ensuring these guidelines incorporate findings from national surveys of minority and adult patient communities.
Committee Categories
Health and Social Services
Sponsors (30)
Amy Klobuchar (D)*,
Michael Bennet (D),
Roy Blunt (R),
Cory Booker (D),
Barbara Boxer (D),
Sherrod Brown (D),
Maria Cantwell (D),
Thad Cochran (R),
Susan Collins (R),
Chris Coons (D),
Al Franken (D),
Kirsten Gillibrand (D),
Lindsey Graham (R),
Tom Harkin (D),
Johnny Isakson (R),
Angus King (I),
Frank Lautenberg (D),
Patrick Leahy (D),
Ed Markey (D),
Bob Menendez (D),
Barbara Mikulski (D),
Bill Nelson (D),
Mark Pryor (D),
Bernie Sanders (I),
Chuck Schumer (D),
Jeanne Shaheen (D),
Debbie Stabenow (D),
Jon Tester (D),
Elizabeth Warren (D),
Roger Wicker (R),
Last Action
Placed on Senate Legislative Calendar under General Orders. Calendar No. 478. (on 07/23/2014)
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| Document Type | Source Location | Created |
|---|---|---|
| BillText | http://gpo.gov/fdsys/pkg/BILLS-113s315rs/pdf/BILLS-113s315rs.pdf | 07/25/2014 |
| Bill | http://gpo.gov/fdsys/pkg/BILLS-113s315rs/pdf/BILLS-113s315rs.pdf.pdf | 07/25/2014 |
| BillText | http://gpo.gov/fdsys/pkg/BILLS-113s315is/pdf/BILLS-113s315is.pdf | 03/06/2013 |
| Bill | https://www.congress.gov/bill/113th-congress/senate-bill/315/all-info | 03/06/2013 |
| Bill | http://gpo.gov/fdsys/pkg/BILLS-113s315is/pdf/BILLS-113s315is.pdf.pdf | 02/27/2013 |
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