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.
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.