The proposed bill establishes a 20-member Endometriosis Working Group within the Legislative Department of Connecticut, aimed at evaluating and making recommendations on various aspects of endometriosis, including diagnosis, treatment, research, education, and public awareness. The group will assess the prevalence and impact of endometriosis in the state, identify barriers to timely diagnosis, evaluate access to evidence-based treatments, and examine insurance coverage and workplace implications. Members will be appointed by legislative leaders and will include healthcare professionals, patient advocates, and individuals with expertise in health equity. The group is required to meet quarterly and report its findings and recommendations to the Governor and relevant legislative committees annually, starting January 1, 2027. The bill introduces new legal language to establish the working group and allows for reimbursement of necessary expenses incurred by members, with no deletions from current law.

Additionally, the bill specifies that the working group will include new members such as a state resident diagnosed with endometriosis and a patient advocate representing individuals with endometriosis. Appointed members will serve staggered terms, with initial appointments required within 30 days of the bill's passage. The executive director of the Commission on Women, Children, Seniors, Equity and Opportunity (CWCSEO) will schedule the first meeting within 60 days of the bill's passage and provide administrative support. The bill emphasizes the importance of diverse representation, including experts in health equity and community-based organizations, to ensure comprehensive perspectives in addressing endometriosis.