Across the world millions of people are suffering from a disease called Myalgic Encephalomyelitis, a debilitating energy-limiting neuroimmune disease that can leave people severely disabled. There are no FDA approved treatments for ME/CFS. Despite this, the Myalgic Encephalomyelitis community is a powerful global force of passionate and loving people, deserving of care and treatment. A segment of our BBI work is dedicated to uplifting the voices of those most disabled by this disease. We aim to bring awareness to this disease, and to spur action towards treatment and support.
To learn more about Myalgic Encephalomyelitis please visit the following websites:
Bateman Horne Center | ME Action Network | Health Rising
Ongoing Opportunities
To participate in our study on rest and ME/CFS please visit restandmecfs.com.
Upcoming Event
Presentation at the Yale Symposium for Disability and Accessibility on April 10th, 2026.
Community Board
As part of our post-election event we created a community sketch board for people to grieve, dream, and rage. Visit the encrypted and anonymous board to read notes from your peers and leave your own. Once you click the link you’ll want to zoom out to view the welcome message. Click the hand icon to move around!
Zine
A mini toolbox for those who may be new to Myalgic Encephalomyelitis. The zine is written from a disability justice perspective.
Click here to access the zine →
Past Events
