This bill mandates the establishment of a comprehensive program to support individuals affected by myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) in Minnesota. It requires the commissioner of health to issue grants aimed at increasing awareness and understanding of ME/CFS among healthcare professionals, patients, and the general public. The bill outlines the process for awarding these grants, which may be given to community health boards, state agencies, or nonprofit organizations, and emphasizes the importance of consulting with members of the ME/CFS community during the grant process. Additionally, the commissioner of human services is tasked with awarding grants to improve access to social services for individuals experiencing ME/CFS.

The bill also establishes a ME/CFS program to conduct community assessments and epidemiological investigations to monitor the impacts of ME/CFS and related conditions. It requires a report to be submitted to the legislature by December 1, 2027, detailing the effectiveness of the grants and identifying areas of need for diagnosis, treatment, and access to services. The bill includes appropriations for these initiatives, ensuring funding is available until June 30, 2028, to support the ongoing efforts to address the challenges faced by individuals with ME/CFS.