HEARD Act of 2025
Sponsor

Full profile: /officials/S001159
Source: Congress.gov · FEC
Cosponsors (5)
Members who have signed on to support this bill since introduction. Source: Congress.gov.
5 cosponsors on record at Congress.gov. The named list is syncing into Govwatch and will appear here shortly — view on Congress.gov in the meantime.
Latest Action
The most recent step in the bill's legislative path. Committee Activity below shows referrals and reports; the full action-by-action history including floor proceedings lives at Congress.gov →
Referred to the Committee on Energy and Commerce, and in addition to the Committees on Ways and Means, and Natural Resources, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.
2025-02-27
Source: Congress.gov
Committee Activity
Currently in
- House Committee on Natural ResourcesReferred To · 2025-02-27
- House Committee on Ways and MeansReferred To · 2025-02-27
- House Committee on Energy and CommerceReferred To · 2025-02-27
Plain-English Summary
Health Equity and Rare Disease Act of 2025 or the HEARD Act of 2025 This bill establishes Department of Health and Human Services (HHS) grants and other initiatives to address rare diseases or conditions (e.g., those affecting less than 200,000 people in the United States) in racial and ethnic minority populations. For example, to advance such purposes, the bill establishes within HHS grants to public and private nonprofit entities for data collection and public outreach, grants to health professions schools to improve health care and minority representation in research regarding rare diseases and conditions, grants to tribal epidemiology centers and tribal and urban Indian health centers for research regarding rare diseases and conditions in tribal communities, scholarships and educational loan repayment for medical school students who agree to work as health care professionals serving populations with rare diseases or conditions, initiatives to coordinate research and other activities across the National Institutes of Health, and public health awareness and education campaigns. Also, the bill requires HHS to submit various reports to Congress on topics including (1) the federal government’s research and public health activities regarding rare diseases or conditions in minority populations, (2) regulatory barriers to treating rare diseases in Medicare beneficiaries of color, and (3) strategies for research and development of treatments for rare diseases or conditions that disproportionately impact minority populations.
Plain-English rewrite of the Congressional Research Service summary published on Congress.gov. Cached and reviewed.
Subjects
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