Endometriosis CARE Act

The Endometriosis CARE Act (HR 8565) directs the National Institutes of Health to fund research and data collection on endometriosis, including $50 million annually from 2025-2029 for studies on treatments and potential cures. It requires the Department of Health and Human Services to analyze barriers to treatment access - like insurance coverage and provider shortages - and report findings within two years. The bill also mandates public education campaigns about endometriosis, with a focus on underserved racial/ethnic groups, and funds provider training on evidence-based care. Additionally, it authorizes a National Academies study on health disparities related to endometriosis diagnosis and treatment. The law directly affects people with endometriosis, healthcare providers, and research institutions through new federal funding and data collection requirements.