Bill > HF3076

This bill establishes a comprehensive approach to supporting individuals with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) in Minnesota through three main initiatives. First, the commissioner of health will award grants to increase awareness and understanding of ME/CFS, focusing on education for healthcare professionals, diagnosed individuals, and the general public. These grants can be given to community health boards, state agencies, state councils, or nonprofit corporations, with input from ME/CFS community members. The grants will support efforts to improve educational materials, raise awareness about ME/CFS symptoms, diagnosis, and treatment, and increase public understanding of available resources. Second, the commissioner of human services will issue grants to improve access to social services for individuals with ME/CFS, including supportive counseling, health education, care coordination, transportation services, financial assistance, workplace accommodations, and support groups. Both grant programs prioritize outreach to marginalized and underserved communities. Third, the bill mandates the establishment of an ME/CFS program to conduct community assessments and epidemiologic investigations, tracking trends in incidence, prevalence, health outcomes, and demographics of those affected. The bill requires a comprehensive report to the legislature by December 1, 2027, detailing the grants' effectiveness, areas of need, and recommended actions. Additionally, the bill appropriates funding for these initiatives in fiscal year 2026, with funds available until June 30, 2028.

Health and Social Services

https://www.revisor.mn.gov/bills/bill.php?b=House&f=HF3076&ssn=0&y=2025