Just because you can’t leave the house, doesn’t mean you can’t change the world.
I have been so impressed with #MEAction, and I bet you will be too. An international network of people with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome.
They are running all kinds of interesting, creative and groundbreaking projects (bonus: they are also super nice).
Get in on the action:
Get the #MEAction newsletter to track all major news and actions.
Get daily updates of all the latest news in research and advocacy.
#MEAction is always looking for patient volunteers and healthy ME allies.
Join a Facebook group with patients and allies to plan and launch new projects.
#MEAction is designed to allow anyone to contribute. Share an action, a news item, or an opinion piece
Create a petition or organize an event.
Join in the global protest for ME rights
Watch the film or host a screening. Directed by Jen Brea, co-founder of #MEAction
Help build this crowd-sourced ME-pedia.
Join in the BedFest. The name says it all.
Share your experiences living with ME/CFS
#MEAction is an international network of patients empowering each other to fight for health equality for Myalgic Encephalomyelitis.
#MEAction is not structured like a traditional advocacy organization. We are a platform designed to empower patients advocates and organizations, wherever they might be, with the technological tools and training to do what they are already doing – better.
We were founded with the belief that while we may find it difficult to advocate for ourselves in the physical world, in the virtual world, we can be an unstoppable force.
How to Get On 