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 enhancing education and outreach about ME/CFS, targeting healthcare professionals, individuals diagnosed with the condition, and the general public. The bill outlines the process for awarding these grants, which includes developing requests for proposals in consultation with the ME/CFS community and providing technical assistance to ensure effective outreach, particularly in underserved areas. Additionally, the commissioner of human services is tasked with awarding grants to improve access to social services for individuals affected by ME/CFS.

The bill also establishes a ME/CFS program to conduct community assessments and epidemiological investigations to monitor the condition's impact, aiming to identify trends and inform public health strategies. A report is required by December 1, 2027, detailing the effectiveness of the grants and the program, along with recommendations for legislative action to improve ME/CFS outcomes. The bill includes appropriations for these initiatives, ensuring funding is available until June 30, 2028, to support the ongoing efforts to address the needs of individuals affected by ME/CFS.