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H.Con.Res.147 / 111th Congress

Expressing the sense of Congress regarding people in the United States with bleeding disorders.

Referred to the Subcommittee on Health.

Official summary

Version 00 · Introduced in House · Jun 11, 2009

Expresses the sense of Congress regarding the federal government's responsibility with respect to research, funding, access to treatment, public education and awareness, and support for screening for bleeding disorders.

Calls for: (1) the Director of the National Institutes of Health (NIH) to provide Congress with a five-year research plan for people with bleeding disorders; (2) the Director of the Centers for Disease Control and Prevention (CDC) to continue to improve outreach, treatment, and prevention for such disorders by facilitating an educational relationship between treatment centers, university health clinics, and undergraduate student populations; and (3) referrals of people with bleeding disorders to federally sponsored hemophilia treatment centers as critical to comprehensive treatment of such disorders.

Urges: (1) physicians to screen all women presenting with menorrhagia for von Willebrand's disease; (2) patient advocate organizations and medical specialty societies to continue to collaborate on public education campaigns about bleeding disorders; and (3) physicians to screen all adolescents attending institutions of higher education for von Willebrand's disease.

Read the summary on Congress.gov
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Who introduced it

Rep. McCarthy, Carolyn [D-NY-4] · D–NY

Committees

  • Energy and Commerce Committee
9 cosponsorship records, including any withdrawals

Actions

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  1. Referred to the Subcommittee on Health.

  2. Referred to the House Committee on Energy and Commerce.

  3. Introduced in House

  4. Introduced in House

Bill text & related measures

Text links open the official source. We currently store references to these documents.

Related bills identified by Congress.gov

No related bills are listed in this snapshot. This does not establish whether the proposal has appeared in earlier Congresses.

Source last updated: Jan 2, 2025. Consult Congress.gov for the current record.

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Neutral evidence review

Objective

Analyze H.Con.Res.147 as objectively as possible. Explain its main provisions, who would be affected, possible benefits and harms, implementation, exceptions, and uncertainties. Present the strongest arguments for and against it, and identify evidence needed to assess its public impact.

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Fairness and public impact

Progressive lens

Examine H.Con.Res.147 through a progressive lens, focusing on fairness, access, economic inequality, and effects on vulnerable communities. Explain potential benefits, costs, and unintended consequences. Consider the strongest counterarguments and distinguish stated goals from demonstrated outcomes.

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Institutions and government scope

Conservative lens

Examine H.Con.Res.147 through a conservative lens, focusing on fiscal responsibility, institutional stability, federalism, and the scope of government. Explain potential benefits, costs, and unintended consequences. Consider the strongest counterarguments and any provisions that challenge this perspective.

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Individual rights and government power

Liberty lens

Examine H.Con.Res.147 through a civil-liberties and limited-government lens. Consider individual rights, privacy, voluntary choice, accountability, and government power. Explain tradeoffs, possible safeguards, and the strongest counterarguments without assuming the proposal is beneficial or harmful.

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