Sharing the journey of awareness, education, and support for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.
Our Mission
The Minnesota ME/CFS Alliance, formed in 2017, is dedicated to serving Myalgic Encephalomyelitis / Chronic Fatigue Syndrome patient and caregiver needs through support, advocacy, and generating enhanced medical care options. We work to unify the ME/CFS community, actively expand awareness of this disease, and educate the healthcare professionals. Our goals are to promote a timely diagnosis with qualified medical support, alleviate patient suffering, and support research for a cure for this underserved and vulnerable population.
Dedicated to change
We are committed to changing the landscape for the estimated 17,000 to 42,000 Minnesotans with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome. Through support for lives affected, advocacy, clinician education, and research we hope to end decades of neglect for this devastating, invisible illness that leaves 75% unable to work, including 25% home or bedbound. Please join us as we make the seemingly impossible possible.