A Message to the ME/CFS Community
In 2017, we founded Minnesota's first organization dedicated to supporting people with ME/CFS. Nearly ten years later, it's with mixed emotions that we've made the difficult decision to formally close the Minnesota ME/CFS Alliance—not because our mission is finished, but because Minnesota now has a far stronger foundation of resources and awareness than when we began.
When we first formed, we could barely find one doctor in the state willing to treat ME/CFS patients. Over the years, so much has changed—including the formation of Dr. Tam's ME/CFS Clinic in Minnesota. Thanks in large part to her tireless work and commitment, more Minnesotans are now finding effective care from providers across the state—something that was desperately needed.
We also spent nearly a decade raising awareness at the community, city, state, and national levels. We connected with dozens of individuals and families through personal support, support groups, quarterly book clubs, and Millions Missing awareness events that featured various guest speakers, including from Mayo Clinic, Dr. Tam, and MEAction. Together, we secured city and state proclamations recognizing ME/CFS Awareness Day—proof of what our collective voice could achieve. We provided personal testimony (virtual, written and in person) at the Minnesota State Capitol with #MEAction MN. We even brought our advocacy to Washington, D.C., participating in Day on the Hill. We brought awareness to the disease through numerous articles written throughout the years about the challenges faced by people like us.
But our greatest accomplishment was simpler: creating a safe place where people with ME/CFS could find others who truly understood. That validation, compassion, and hope are a bond we're proud to have fostered. While the organization is closing, the friendships, knowledge, and community we built together will endure.
Thank you for letting us be part of your journey.
With heartfelt gratitude,
The Minnesota ME/CFS Alliance Board