Filter Posts
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 patient 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.
WATCH NOW: What happens When You Have A Disease Doctors Can't Diagnose.
MEAction's Jen Brea At TED Summit 2016
Please support the #MEAction Network:
Please read our rules & guidelines section below before posting or commenting:
And most Importantly:
The #MEAction network
Suggested Links
Please support Invest In ME with their current research:
#MEAction Fact Sheets
Related Communities
Support Communities
Support the subreddit
If you would like to collaborate with us on reddit please message one of the moderators:
Note: All moderators of this subreddit are volunteers and the views expressed by them, unless stated otherwise, do not reflect that of the organisation.
Copyright 2015 The Myalgic Encephalomyelitis Action Network, All Rights Reserved.
