Show your Solidarity with the #MillionsMissing on May 12th – Protest Virtually

The #MillionsMissing are taking to the streets in 17 cities across the world on Friday, May 12th to once again demand change for people with Myalgic Encephalomyelitis (ME).

Join the protest virtually

Show your solidarity for the #MillionsMissing movement from your bed by laying out your empty shoes (to represent the life your are missing due to ME), take a photo and share it on social media with the hashtag #MillionsMissing. If you are comfortable, write a note about how the disease has impacted your life. For one day, let us be visible together.
[button_color url=”http://meaction.net/virtual-protest/” content=”Join the #MillionsMissing Virtually” target=””]  

 
 
Learn more about the  #MillionsMissing global Day of Action on May 12th.

Facebook
Twitter
WhatsApp
Email

3 thoughts on “Show your Solidarity with the #MillionsMissing on May 12th – Protest Virtually”

  1. Houston will be lighting up their city hall this May 11, 12 and 13 for MECFS Awareness Day.

Comments are closed.

Latest News

a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.

Severe ME Artists Project 2024

Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by

Read More »
Light blue square with rainbows in the top left and bottom right corner. In the middle are the words, -Pride is Valid- No Matter How One Celebrates or Experiences It. #MEAction Board Member, Jennifer England, shares her views on Pride. The #MEAction logo in the top right corner.

Pride Is Valid No Matter How One Celebrates or Experiences It

In honor of Pride Month, #MEAction is sharing a heartfelt message from our board member, Jennifer England, about what Pride means to her and her wife who lives with severe ME. My wife and I have both been queer our whole lives, but in the 70s that was the quiet part you didn’t say out

Read More »

Questions to Ask Prospective MPs About ME/CFS

In the next few weeks, candidates will be knocking on doors seeking votes for the upcoming UK Election. It’s important that candidates from all parties are made aware of the challenges facing people with ME and Long Covid. It can be a little daunting to be unprepared so here are some questions you might want

Read More »
Scroll to Top