other to fight for health equality for Myalgic Encephalomyelitis.
#MEAction is not structured like a traditional advocacy organization
or patients’ association. We are primarily 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.