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Endometriosis CARE Act: Boosting Research, Awareness, and Treatment Access

This bill aims to improve the lives of individuals with endometriosis by significantly increasing funding for research (up to $50 million annually) to find better treatments and a cure. It mandates an analysis of barriers to accessing care, including insurance coverage gaps and costs, which could lead to easier access to necessary healthcare services. Furthermore, the Act establishes public and professional education programs to improve early detection and the quality of treatment.
Key points
Increased Research Funding: Authorizes $50 million annually (2025-2029) for the National Institutes of Health to conduct research on endometriosis, including developing better treatments and a cure.
Identifying Access Barriers: Requires the government to analyze why patients face difficulties accessing treatment (e.g., lack of insurance coverage, high costs, provider shortages) to help remove these obstacles.
Public and Professional Education: Establishes public awareness campaigns and disseminates information to healthcare providers to improve diagnosis, care quality, and support for patients.
Study on Disparities: Mandates a study by the National Academies on disparities in endometriosis prevalence, detection, and treatment outcomes based on race, ethnicity, and insurance status.
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Additional Information
Print number: 118_HR_8565
Sponsor: Rep. Williams, Nikema [D-GA-5]
Process start date: 2024-05-23
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Summarized by: gemini-flash-latest
Source data: api.congress.gov
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OFFICIAL LEGAL TITLE

Endometriosis CARE Act

FREQUENTLY ASKED QUESTIONS

What is the official ID of this bill?

The official print number for this legislation is 118_HR_8565.

Which chamber initiated this legislation?

This legislation was initiated in the House of Representatives.

When did the legislative process begin?

The process officially started on 2024-05-23.

What are the main provisions?

Key points include:

  • Increased Research Funding: Authorizes $50 million annually (2025-2029) for the National Institutes of Health to conduct research on endometriosis, including developing better treatments and a cure.
  • Identifying Access Barriers: Requires the government to analyze why patients face difficulties accessing treatment (e.g., lack of insurance coverage, high costs, provider shortages) to help remove these obstacles.
  • Public and Professional Education: Establishes public awareness campaigns and disseminates information to healthcare providers to improve diagnosis, care quality, and support for patients.
  • Study on Disparities: Mandates a study by the National Academies on disparities in endometriosis prevalence, detection, and treatment outcomes based on race, ethnicity, and insurance status.
What is the specific legal status?

The current status is Expired.

Where can I read the full text of this legislation?

The full official text is available at: View full text

Who is the primary sponsor?

The primary sponsor is Rep. Williams, Nikema [D-GA-5].

What is the latest detailed status?

The latest detailed status is: Referred to the Subcommittee on Health.

Is this summary verified?

Yes. This content was analyzed by AI and verified by the Lustra Judge System on 2025-12-30.

CATEGORIES

Health