HR 6682

0likes☆Favorite🔕SubscribeShare

Introduced ↻ Update bill dataRe-checks Congress.gov for new actions and updates the bill's status, and fills in any sponsors, committees, or related bills that are missing. It does not re-pull sponsors/cosponsors/committees/related — those rarely change — and it skips all work if nothing has changed upstream, so it's cheap to click. Contact your reps Urge the sponsor

IN THE HOUSE OF REPRESENTATIVES

December 11, 2025

Ms. Williams of Georgia (for herself, Ms. Underwood, Ms. Adams, Mr. Cisneros, Ms. Clarke of New York, Ms. Friedman, Mr. Frost, Mr. Goldman of New York, Mr. Hernandez, Mr. Kennedy of New York, Mrs. McIver, Ms. Norton, Mr. Pocan, Mr. David Scott of Georgia, Ms. Tlaib, Mr. Tonko, Mrs. Watson Coleman, Mr. Bishop, Mr. Moulton, Ms. Brown, Ms. Lofgren, and Mr. Gottheimer) introduced the following bill; which was referred to the Committee on Energy and Commerce

A BILL

To advance research, promote awareness, and provide patient support with respect to endometriosis, and for other purposes.

Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,

SECTION 1. SHORT TITLE.

This Act may be cited as the “Endometriosis Coverage, Awareness, Research, and Education Act” or the “Endometriosis CARE Act”.

SEC. 2. FINDINGS.

The Congress finds as follows:

(1) Endometriosis is a disease in which tissue similar to the lining of the uterus grows outside the uterus. It can cause severe pain in the pelvis and make it harder to get pregnant. Endometriosis often causes severe pain in the pelvis, especially during menstrual periods. Some people also have pain during sex or when using the bathroom. Some people have trouble getting pregnant.

(2) It causes a chronic inflammatory reaction that may result in the formation of scar tissue (adhesions, fibrosis) within the pelvis and other parts of the body. The cause of endometriosis is unknown. There is no known way to prevent endometriosis. There is no cure, but its symptoms can be treated with medicines or, in some cases, surgery.

SEC. 3. ENDOMETRIOSIS COVERAGE, AWARENESS, RESEARCH, AND EDUCATION.

Part F of title IV of the Public Health Service Act (42 U.S.C. 287d et seq.) is amended by adding at the end the following:

“SEC. 486C. ENDOMETRIOSIS COVERAGE, AWARENESS, RESEARCH, AND EDUCATION.

“(a) Advancing Endometriosis Data Collection, Surveillance, and Research.—

“(1) In general.—The Director of NIH shall conduct or support data collection, surveillance, and research related to endometriosis.

“(2) Use of funds.—In carrying out subsection (a), the Director may—

“(A) conduct or support research and related activities regarding endometriosis, including research to improve treatment options and develop a cure for endometriosis;

“(B) establish or expand an internet clearinghouse to catalog existing endometriosis research, treatment options, and related information for patients and health care professionals; or

“(C) carry out related activities as determined by the Director.

“(3) Authorization of appropriations.—To carry out this subsection, there is authorized to be appropriated $50,000,000 for each of fiscal years 2026 through 2030.

“(b) Identifying Barriers to Accessing Treatments for Endometriosis Symptoms.—

“(1) Research.—The Secretary shall conduct an analysis of barriers that individuals diagnosed with endometriosis face in accessing treatments for endometriosis symptoms, including transportation barriers and barriers caused by health care professional shortages.

“(2) Topics.—In carrying out the analysis under paragraph

(1), the Secretary may—

“(A) assess data from the Transformed Medicaid Statistical Information System related to services furnished to individuals diagnosed with endometriosis for the treatment of endometriosis symptoms under State Medicaid programs under title XIX of the Social Security Act and Children’s Health Insurance Programs under title XXI of such Act; and

“(B) assess data related to services furnished to individuals diagnosed with endometriosis for the treatment of endometriosis symptoms under group health plans or group or individual health insurance coverage offered by a health insurance issuer (as those terms are defined in section 2791).

“(3) Data collection.—To carry out the analysis under paragraph (1), the Secretary may require—

“(A) group health plans or issuers of group or individual health insurance coverage to provide such information as may be required to assess barriers that individuals diagnosed with endometriosis face in accessing treatments for endometriosis symptoms, including a lack of insurance coverage or cost-sharing requirements for such treatments; and

“(B) State Medicaid programs and Children’s Health Insurance Programs to collect and report data related to services furnished to individuals diagnosed with endometriosis for the treatment of endometriosis symptoms through the Transformed Medicaid Statistical Information System, including data stratified by relevant demographic characteristics.

“(4) Privacy requirements.—In carrying out the analysis under paragraph (1), the Secretary shall ensure that the privacy and confidentiality of individual patients are protected in a manner consistent with relevant privacy and confidentiality laws.

“(5) Report.—Not later than two years after the date of enactment of this section, the Secretary shall submit to the Congress, and make publicly available on the website of the Department of Health and Human Services, a report on the analysis carried out under this subsection.

“(c) Education and Dissemination of Information With Respect to Endometriosis.—

“(1) Endometriosis public education program.—The Secretary shall develop, and disseminate to the public, information regarding endometriosis, including information on—

“(A) the awareness, incidence, and prevalence of endometriosis, with a particular focus on individuals from racial and ethnic minority groups (as defined in section 1707(g)) and other underserved groups;

“(B) culturally and linguistically appropriate support that is available to address the mental health impacts of endometriosis; and

“(C) the availability, as medically appropriate, of the range of treatment options for symptoms of endometriosis.

“(2) Dissemination of information.—The Secretary may disseminate information under paragraph (1) directly or through arrangements with intra-agency initiatives, nonprofit organizations, consumer groups, institutions of higher education (as defined in section 101 of the Higher Education Act of 1965), or Federal, State, or local public private partnerships.

“(3) Authorization of appropriations.—To carry out this subsection, there is authorized to be appropriated $2,000,000 for each of fiscal years 2026 through 2030.

“(d) Information to Health Care Providers With Respect to Endometriosis.—

“(1) Dissemination of information.—The Secretary shall, in consultation with relevant health care professional societies and associations, disseminate information to health care professionals, health care-related organizations, and health systems to promote evidence-based care for individuals with endometriosis, including information related to—

“(A) detecting and diagnosing endometriosis;

“(B) providing care for individuals with endometriosis;

“(C) communicating with patients about endometriosis; and

“(D) related topics.

“(2) Authorization of appropriations.—To carry out this section, there is authorized to be appropriated $2,000,000 for each of fiscal years 2026 through 2030.

“(e) Endometriosis Disparities Study Through National Academies.—

“(1) In general.—The Secretary shall seek to enter an agreement, not later than 90 days after the date of enactment of this section, with the National Academies of Sciences, Engineering, and Medicine (referred to in this section as the ‘National Academies’) under which the National Academies agree to conduct a study on endometriosis disparities.

“(2) Study requirements.—The agreement under paragraph

(1) shall direct the National Academies to—

“(A) assess endometriosis prevalence, detection, treatment, and outcome disparities by race, ethnicity, geography, primary language, sexual orientation, gender identity, disability status, and insurance status, and related topics as determined by the Secretary; and

“(B) make recommendations to the Congress, Federal agencies, health care professionals, and other relevant stakeholders based on the National Academies’ findings pursuant to subparagraph (A).

“(3) Report.—The agreement under paragraph (1) shall direct the National Academies to complete the study under this section, and transmit to the Congress and make publicly available a report on the results of the study, not later than 24 months after the date of enactment of this section.

“(4) Authorization of appropriations.—To carry out this subsection, there is authorized to be appropriated $500,000.”. <all>