#MEAction Continues to Get Press for ME

#MEAction continues to prioritize getting ME in the press. We are very thankful to be featured in USA Today, North Jersey, New York Times, Infection Control Today, Times-Herald and Well+Good, all in the last few weeks! 

Our press reach continues to focus on multiple audiences, including scientists and medical practitioners, the disability and chronic illness community, and the general public. 

Good press matters and it affects our advocacy. Bad press matters too because it allows us to correct and educate journalists (or those interviewed if they get it wrong)- and we do! We are contacting every single journalist writing about Long COVID to educate them about ME. To date, we’ve contacted over 2,385 journalists about ME. 

In case you missed the publications, we encourage you to read and share with your networks. 

To read the articles, click on one of the images below.

Press is a crucial part of mobilizing a growing community and ensuring that people with ME get the treatment and care they deserve. 

Onward,
Laurie, Ben, Holly, Erin, Jaime, and Steven

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#NotJustFatigue Video Series: Interview with Creator Elizabeth Ansell

Over the past year, the #NotJustFatigue website, created by Elizabeth Ansell, releases a 10-part, documentary style, short form video series on different aspects involved in living with ME. Titles of the videos include topics such as: You Have No Idea How Serious This Is, Nobody Believes ME, and It’s Not Hysteria: It’s Sexism. In these

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#MEAction Georgia: Voice of the Patient in Coordination with CDC & Emory School on Nursing

Back in September, #MEAction Georgia State Chapter partnered with the Centers for Disease Control and Prevention (CDC) and Emory School of Nursing to host, Voice of the Patient: A Panel Discussion with #MEAction Georgia. This event was a continuation of #MEAction Georgia’s #MillionsMissing 2024: #TeachMETreatME programming. Erin Lee and Liz Burlingame of the #MEAction Georgia

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Home Test To Treat – Findings Summary

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