This bill mandates the establishment of a comprehensive program to address 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 grants will support educational outreach and the development of resources for those affected by ME/CFS. Additionally, the commissioner of human services is tasked with awarding grants to improve access to social services for individuals experiencing the effects of ME/CFS. Both commissioners are required to consult with members of the ME/CFS community during the grant process and provide technical assistance to ensure effective outreach, particularly in underserved areas.

Furthermore, the bill establishes a ME/CFS program to conduct community assessments and epidemiological investigations to monitor the impact of ME/CFS and related conditions. It mandates a report to the legislature by December 1, 2027, detailing the effectiveness of the grants and identifying additional needs for diagnosis, treatment, and access to services. The bill also includes appropriations for the grants and program activities, ensuring funding is available until June 30, 2028.