#MillionsMissing 2022 Will be in Two Parts

This year, we are excited to announce that #MillionsMissing will be held in two parts: May and September!

#MillionsMissing is about demonstrating our community’s collective refusal to let the stories of people with ME be erased, or access to healthcare and medical research blocked. We protest against all barriers to justice for the growing community of people with ME, including those affected by Long COVID and other complex chronic conditions.

In May, we will focus on coming together virtually to celebrate our vibrant community through support, art, and empowerment.

In September, our goal will be to gather in person, in ways that are safe to do so, and use the power of our collective action to win widespread attention for the health justice we all need.

Both #MillionsMissing events will have virtually-accessible components because your participation is critical to this movement, no matter your health or ability level.

We invite you to participate in both events to focus on community gathering in May and outward action in September. There will be actions in both the UK and the US and options to get involved and take action across the globe.

Add to Your Calendar Now:
SAVE May 12th for a #MillionsMissing Community Event

And we will be in touch about September actions and events as the timeline for the year becomes clearer.
 
With the millions more people being diagnosed with ME, now is the time to take action together, and fight for real, lasting change.
 
In solidarity,
All of us at #MEAction
Facebook
Twitter
WhatsApp
Email

2 thoughts on “#MillionsMissing 2022 Will be in Two Parts”

    1. Hi, Alyssa!

      The Virtual Choir will be publicly available soon, and we will announce it once it’s published, so keep an eye out!

Comments are closed.

Latest News

black square image with two white lines at the top and bottom of the image. Then another two white lines come out from the sides to the middle over the #MEAction logo and the words, #NotJustFatigue Video Series Elizabeth Ansell Interview.

#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

Read More »
navy blue square. there are two white lines at the top and bottom of the square. The #MEAction logo in at the top of the image. The words #MEAction Georgia Voice of the Patient in coordination with the Center for Disease Control and Prevention & Emory School of Nursing.

#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

Read More »
a light blue square image with medical instruments/tools as a border (pill bottles, scales, needles, covid protein spike, etc). At the top of the image is the Home Test to Treat Program logo, in blue font: Findings Summary. Below that the #MEAction logo and Body Politic Logo.

Home Test To Treat – Findings Summary

#MEAction and Body Politic collaborated last spring, with a new national telehealth program, Home Test to Treat. We are now able to share initial findings from the program! Here are some highlights: 80K + enrolled in the program across the country! 40K + test distributed 6K + individuals treated for COVID-19 or flu 5.6K+ organizations

Read More »
Scroll to Top