Sharing the journey of awareness, education, and support for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.
The Minnesota ME/CFS Alliance 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.
The Basics: A Guide to Learning, Sharing and Making a Difference in Chronic Fatigue Syndrome (ME/CFS)
by Cort Johnson. December 18, 2018
In 2018 chronic fatigue syndrome (ME/CFS) finds itself in an unsettling place: it’s a common, serious disease that can cause profound levels of disability and distress but which gets little respect or funding. Read more.
Minnesota ME/CFS on Twitter
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.