About
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.
UPCOMING EVENTS
Monthly planning meeting – We meet virtually for one hour and have the following meetings coming up:
Thursday, May 18th at 5:30pm CT. This meeting will feature a special guest, Kate Murray, MPH (she/her), from the Minnesota Dept. of Health.
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!