Minnesota State Chapter listed across a photo a lighthouse on a cliff. #MEAction logo in the bottom right corner


The #MEAction Minnesota chapter focuses on policy and advocacy. We advocate for our rights and recognition, bring awareness to this disease, and work with elected officials, medical providers, and others to make sure Minnesota recognizes ME/CFS and provides quality care and support to all. 

Each month we will plan and organize for action and we need and welcome your help. We will be working with elected officials, medical providers, and fellow citizens to ensure we are recognized, understood and supported in MN. 

We welcome anyone with ME/CFS, caregivers, family members and allies looking to help us amplify our needs and work to make MN a place that cares for us and other citizens with similar often-invisible diseases. 


Monthly planning meeting – We meet virtually for one hour and have the following meetings coming up:

#Millions Missing 2024 planning meetings:
Saturday, March 16th: 1:00-2:00 pm central
Saturday, March 30th: 2:00-3:00 pm central 
Please contact Terri Wilder at [email protected] for the web link to join these planning meetings. 
Terri L Wilder, MSW 




For questions please contact our chapter leader: 

Terri L Wilder, MSW: [email protected]

Scroll to Top