Sec. 3. Endometriosis coverage, awareness, research, and education
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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: The Director of NIH shall conduct or support data collection, surveillance, and research related to endometriosis. In carrying out subsection (a), the Director may— conduct or support research and related activities regarding endometriosis, including research to improve treatment options and develop a cure for endometriosis; establish or expand an internet clearinghouse to catalog existing endometriosis research, treatment options, and related information for patients and health care professionals; or carry out related activities as determined by the Director.
To carry out this subsection, there is authorized to be appropriated $50,000,000 for each of fiscal years 2026 through 2030. 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. In carrying out the analysis under paragraph (1), the Secretary may— 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 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).
To carry out the analysis under paragraph (1), the Secretary may require— 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 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.
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. 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.
The Secretary shall develop, and disseminate to the public, information regarding endometriosis, including information on— 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; culturally and linguistically appropriate support that is available to address the mental health impacts of endometriosis; and the availability, as medically appropriate, of the range of treatment options for symptoms of endometriosis.
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. To carry out this subsection, there is authorized to be appropriated $2,000,000 for each of fiscal years 2026 through 2030. 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— detecting and diagnosing endometriosis; providing care for individuals with endometriosis; communicating with patients about endometriosis; and related topics. To carry out this section, there is authorized to be appropriated $2,000,000 for each of fiscal years 2026 through 2030. 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. The agreement under paragraph
(1)shall direct the National Academies to— 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 make recommendations to the Congress, Federal agencies, health care professionals, and other relevant stakeholders based on the National Academies’ findings pursuant to subparagraph (A). 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. To carry out this subsection, there is authorized to be appropriated $500,000. .
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Sec. 3
Endometriosis coverage, awareness, research, and education
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