Legislative Priorities

The Children’s Cardiomyopathy Foundation (CCF)’s advocacy effort is focused on saving lives and improving the quality of life for children with cardiomyopathy and their families. CCF has been active on a variety of federal and state advocacy issues, with the primary focus on federal legislation.

Our Advocacy Focus

CCF’s federal advocacy work is focused on these priorities:

  • Increasing cardiomyopathy research
  • Promoting public awareness and education
  • Encouraging early and accurate diagnosis
  • Improving survival from sudden cardiac arrest
  • Ensuring access to specialized and quality care

To learn more about CCF’s legislative and health policy agenda, click here.

Key Legislative Initiatives

Over the years, CCF has been actively involved in supporting several legislative initiatives focused on cardiomyopathy and prevention of sudden cardiac death. Individuals can advance cardiomyopathy-related legislation by contacting their congressional representatives and sharing their personal story of how cardiomyopathy has impacted their life. As their constituent, this gives them a compelling reason to support our cause.

Appropriations Language Requests

The Foundation actively encourages Members of Congress to support the needs of those with cardiomyopathy through the inclusion of cardiomyopathy specific language in appropriations bills. Each year, the Senate Appropriations Subcommittee on Defense releases its list of approved research areas for funding under the Department of Defense Peer Reviewed Medical Research Program (PRMRP). Cardiomyopathy was first listed as an approved research topic in 2018 and represents a new source of research funding for pediatric cardiomyopathy that needs to be renewed every year.

Additionally, CCF will request the Labor, Health and Human Services Subcommittees to address the unmet education and awareness needs of the cardiomyopathy community. This includes advocating for the CDC to integrate information about the signs, symptoms, and risk factors of pediatric cardiomyopathy into the Centers for Disease Control and Prevention (CDC) existing programs, including the Division of Heart Disease and Stroke Prevention, the Division of Reproductive Health, the National Center for Birth Defects, and Development Disabilities, and its Division of Population Health. Additionally, CCF asks that Congress encourage the National Heart, Lung, and Blood Institute’s (NHLBI) to continue funding the North America Pediatric Cardiomyopathy Registry.

Cardiomyopathy HEARTS Act

The Cardiomyopathy Health, Education, Awareness, Risk Assessment, and Training in the Schools (HEARTS) Act was first introduced by Representative Frank Pallone, Jr. in December 2011 and Senators Robert Menendez and Frank Lautenberg in February 2012. In September 2017, Representative Frank Pallone (D-NJ) reintroduced the Cardiomyopathy HEARTS Act (H.R. 3880) to help raise awareness of cardiomyopathy across the lifespan and identify undiagnosed children at risk of sudden cardiac arrest. First, the legislation proposes to develop educational materials and resources on cardiomyopathy with the Centers for Disease Control and Prevention (CDC) and disseminating them to school administrators, educators, and families. Second, the bill requests the CDC to collect and analyze data to identify the impact, prevalence, and natural history of cardiomyopathy. Lastly, the bill directs the National Institutes of Health (NIH) to assess the current research needs and projects related to cardiomyopathy. Issue Brief

Take Action on the Cardiomyopathy HEARTS Act

Additional information about CCF legislative priorities can be found on the Public Policy Resources page.

CCF Advocacy Efforts 

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