#MillionsMissing: Videos Created by our Amazing Community

This year’s #MillionsMissing, our community created some amazing videos that we are privileged to highlight. This is just a small sampling of the amazing videos that were shared with us. It would be impossible to include them all, but we thank you all for sharing!

Chronic — Maggie Borgen

M.E. & Friends — Lisa Walker

Wellness Ella

Hannah Avery

Greta Granö (@chronically.greta) & Lizzie Mooney (@lizzie_mooney__)

Alyssa Erin

Vox Jo Hsu @voxjohsu

It’s #meawarenessday and I honestly survived the past years of unexplained suffering through the knowledge archived and shared by @MEActNet + allies, so here’s a brief story.

Shelby Lock & CoRy Wyszynski

Our #MillionsMissing Artist Salon led to two presenters working together to create a video showcasing music and art by Shelby Lock and Cory Wyszynski

Steph101k on YouTube

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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

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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

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Questions to Ask Prospective MPs About ME/CFS

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