The Endometriosis CARE Act is a comprehensive federal initiative to advance treatment and support for endometriosis, a chronic condition where tissue similar to the uterus lining grows outside the uterus, causing severe pain and fertility problems. The bill authorizes $50 million annually from 2025 through 2029 for the National Institutes of Health to conduct research and develop treatment options, along with $2 million yearly for public education and $2 million yearly to educate healthcare providers about detecting and treating the disease. It also requires the Department of Health and Human Services to analyze barriers endometriosis patients face in accessing care, collect insurance data on treatment coverage, and commission an independent study through the National Academies to examine disparities in how the disease affects people of different races, ethnicities, and socioeconomic backgrounds. The bill directs the Secretary to report findings to Congress within two years, with special attention to improving care for underserved communities.
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