Plan for #MillionsMissing Now! Read the Toolkit!

#MillionsMissing 2019 is fast approaching, and now is the time to get started! Demonstrations calling for health equality for Myalgic Encephalomyelitis (ME) will take place around the globe throughout the week of May 5th – 12th, 2019. We are only two months away!

How will you join the movement? Check out our toolkit and determine which level is right for you:

  • Protest on social media
  • Organize or join a small gathering
  • Organize or join a community demonstration
  • Organize or join a citywide demonstration

If you would like to take the lead or help organize a demonstration or event, get in touch with ME activists in your hometown to start communicating about the plan. Find a local #MEAction Facebook group near you, here.

Also, register your demonstration here (even if you just want to pursue the option but aren’t sure on details), and we can help put you in touch with others from your area.

We are encouraging each location to think about how they can make a creative, visual impact this year. One or two simple ideas can make a big difference – we lay it all out in the toolkit!

We’ve made important strides in making our voices heard before our government leaders across the world, but we have much more to do. More than ever, we need to grow our movement and remain persistent in our demands for urgent, sweeping change, for equitable research funding and care, accurate medical education and an end to the harm and stigma.

[maxbutton id=”17″ url=”http://www.meaction.net/wp-content/uploads/2019/03/Step-by-Step-Guide_-MillionsMissing-2019-1.pdf” text=”Read the Toolkit” ]

 

[maxbutton id=”21″ url=”http://www.meaction.net/wp-content/uploads/2019/03/Step-by-Step-Guide_-MillionsMissing-2019-UK-FINAL-Version.pdf” text=”Read the UK toolkit” ]

 

Facebook
Twitter
WhatsApp
Email

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