H.R. 594 · 113th Congress
Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2014
Law · 113-166 · Sep 26, 2014Key: what the circles and colors mean
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Became law without a recorded vote. It passed by voice vote or unanimous consent, which don't record how each member voted.
113 cosponsors · 68 D, 45 R
1 signed on when it was introduced; the rest joined later. Cosponsors who withdrew aren't shown.
- House Introduced Feb 8, 2013
- House Passed Jul 28, 2014
- Senate Passed Sep 18, 2014
- President To the President Sep 23, 2014
- President Signed Sep 26, 2014
- Law Sep 26, 2014
Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2014 - (Sec. 2) Amends the Public Health Service Act to revise the muscular dystrophy research program of the National Institutes of Health (NIH).
What it does: CRS summary · Public Law · Sep 26, 2014
(This measure has not been amended since it was reported to the House on July 24, 2014. The summary of that version is repeated here.)
Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2014 - (Sec. 2) Amends the Public Health Service Act to revise the muscular dystrophy research program of the National Institutes of Health (NIH).
Expands the range of 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.
(Sec. 3) Requires the Secretary of Health and Human Services (HHS), in carrying out epidemiological activities regarding Duchenne and other forms of muscular dystrophy, to ensure that data are representative of all affected populations and shared in a timely manner.
(Sec. 4) Amends the Muscular Dystrophy Community Assistance, Research, and Education Amendments of 2001 to authorize the Secretary to cooperate with professional organizations and the patient community in the development and issuance of care considerations, including acute care considerations, for pediatric and adult muscular dystrophy patients. Authorizes the Secretary, in developing and updating care considerations, to incorporate strategies specifically responding to the findings of the national transitions survey of minority, young adult, and adult communities of muscular dystrophy patients.Written by the nonpartisan Congressional Research Service. All summary versions on Congress.gov
About this bill and sources
Official title: Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2014
Also known as: Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2013
Latest action (Sep 26, 2014): Became Public Law No: 113-166.
Policy area: Health · Origin: House · Introduced: Feb 8, 2013
Official page on Congress.gov · Bill text (GovInfo) · Status record (XML)
- House Introduced Feb 8, 2013
- House Passed Jul 28, 2014
- Senate Passed Sep 18, 2014
- President To the President Sep 23, 2014
- President Signed Sep 26, 2014
- Law Sep 26, 2014
No recorded floor vote found.