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:
Saturday, January 21st at 2:00 pm central
Thursday, February 16th at 5:30 pm central
Thursday, March 9th at 5:30 pm central
Thursday, April 6th at 5:30 pm central.
For more information including video conference link and call-in numbers please look on the #MEAction Events calendar for our upcoming call and join details!