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#MillionsMissing – Minnesota ME/CFS Alliance Virtual Event

The Minnesota ME/CFS Alliance will host a virtual #MillionsMissing event to discuss recent MN ME/CFS events, update our community on our nonprofits’ activities and host a virtual discussion with local long Covid patient, Andy Flosdorf (see recent Star-Tribune article on April 5, 2021.)Here is the link to join the virtual event:

#MillionsMissing Lancaster Virtual Event

Join the Lancaster ME community for their #MillionsMissing 2021 Virtual Event! This will be an opportunity to join together as a community, share our stories, and discuss ways to take action. We can’t wait to see you there.To receive link to attend the virtual event, please email [email protected].

#MillionsMissing MEXICO Virtual Event

Join the Mexico ME community for their #MillionsMissing 2021 Virtual Event! This will be an opportunity to join together as a community, share our stories, and discuss ways to take action. We can’t wait to see you there. Language: Spanish. Here is the link to join the virtual event:

#MillionsMissing: “GatherOUND” Event–Community Meet & Greet

At #MEAction we are all about bringing people together. So we are excited to announce the return of our community Gatheround (previously known as Icebreaker) events for #MillionsMissing! Join the #MEAction community for a fun gathering, where you will be able to connect with people around the globe, participate in easy get-to-know-you games, and chat with …

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Free

#MEAction Maryland #MillionsMissing – Rest Fest Tea Party for M.E.

Join #MEAction Maryland in your PJs with your favorite filled mug & a treat as we discuss ways to rest & recover on Blue Sunday.Here is the agenda for the event: Welcome - rest is productiveWhat is self-care for M.E. discussionBed Yoga demoJoin our #MillionsMissing asksUse this link to join event:

#MEAction Town hall on CDC draft evidence review of ME/CFS treatments

Update: slide deck for town hall The U.S. Centers for Disease Control and Prevention (CDC) published a notice of request for public comments on its systematic review draft report for diagnosis and treatment of ME/CFS which will remain open until August 16, 2021. To learn more about the CDC draft evidence review and #MEAction advocacy …

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Free
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