Short title

This Act may be cited as the

Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2013

Initiative through the Director of the National Institutes of Health

Section 404E of the Public Health Service Act (42 U.S.C. 283g) is amended— (1)in subsection (a)(1)— (A)by striking Muscoskeletal and inserting Musculoskeletal; and (B)by inserting Becker, myotonic, facioscapulohumeral muscular dystrophy (referred to in this section as FSHD), Congenital muscular dystrophy, Limb-girdle muscular dystrophy, after Duchenne,; (2)in subsection (b)— (A)in paragraph (2), by inserting cardiac and pulmonary function, after imaging, genetics,; and (B)in paragraph (3), by inserting and sharing of data after regular communication; (3)in subsection (d)— (A)in paragraph (2)— (i)in the matter preceding subparagraph (A), by striking 15 and inserting 18; and (ii)in subparagraph (A), by striking children with muscular dystrophy, such as the Department of Education and inserting children and adults with muscular dystrophy, such as the Department of Education, the Social Security Administration, the United States Administration for Community Living; and (B)in paragraph (4)(B), by inserting , and shall meet no less than two times per calendar year before the period; (4)in subsection (e)— (A)in paragraph (1)— (i)in the matter preceding subparagraph (A), by striking through the national research institutes and inserting through the agencies represented on the Coordinating Committee pursuant to subsection (d)(2)(A); and (ii)in subparagraph (A), by striking and rehabilitative issues, including studies of the impact of such diseases in rural and underserved communities and inserting public resources, and rehabilitative issues, including studies of the impact of such diseases in rural and underserved communities, health economic studies to demonstrate the cost-effectiveness of providing independent living resources and support to patients with various forms of muscular dystrophy, and studies to determine optimal clinical care interventions for adults with various forms of muscular dystrophy; and (B)in paragraph (2), by adding at the end the following:

(F)The development of clinical interventions to improve the health of adults with various forms of muscular dystrophy.

; and

(5)in subsection (g), by striking for the various forms of muscular dystrophy by prioritizing the achievement of the goals related to this topic in the plan under subsection (e)(1) and inserting and shall, not later than 6 months after the date of enactment of the Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2013, in coordination with appropriate Federal agencies, including relevant offices within the Food and Drug Administration and supported by the National Institutes of Health and Department of Defense, 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.

Surveillance and research regarding muscular dystrophy

Section 317Q of the Public Health Service Act (42 U.S.C. 247b–18) is amended— (1)in the second sentence of subsection (b), by inserting before the period the following: and ensure that the program captures data from different racial and ethnic populations, and that such data are made publicly available to investigators conducting public or private research on muscular dystrophy; and (2)in subsection (c), by adding at the end the following: The Secretary shall also foster ongoing engagement and collaboration between the surveillance program and centers of excellence..

Information and education

Section 5(c) of the Muscular Dystrophy Community Assistance, Research and Education Amendments of 2001 (42 U.S.C. 247b–19(c)) is amended by adding at the end the following:

(4)Update and widely disseminate existing Duchenne-Becker muscular dystrophy care considerations for pediatric patients, develop and widely disseminate Duchenne-Becker muscular dystrophy care considerations for adult patients, and develop and widely disseminate acute care considerations for all muscular dystrophy populations. The care considerations should build upon existing efforts currently underway for congenital muscular dystrophy, fascioscapulohumeral muscular dystrophy, limb-girdle muscular dystrophy, and myotonic 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.