Part 2 of Peggy Munson’s critical review of the film Unrest by Jen Brea.
ME
Jen Brea’s Unrest and the Troubled Language of Languor: Part 1
Part 1 of a critical review of the movie Unrest by author and ME patient/activist Peggy Munson.
The unstoppable Amelia Hill
Long-time Planet Thrive member and survivor of severe environmental illness and myalgic encephalomyelitis, Amelia Hill flies the flag for invisible illness.
Vote today for CFS research – only a few days left
by Cort Johnson | Chase Community Giving has given CFS research a kind of life line; a chance to win some big money in a time of dearth and to put that money directly into the hands of excellent researchers.
Peggy Munson’s new campaign to eradicate XMRV
Just launched: The EXIT Project (Eradicate XMRV Infection Today), is a broad-based group of individuals who do ACT-UP style actions to raise awareness about ME/CFS/XMRV.
The best offense is a good offense: what we need to learn from AIDS
by Peggy Munson | …ME/CFS patients have tended to get sucked into what domestic violence activists call the “cycle of violence,” believing the bullies’ lies that they will change…
New movie: What about ME?
There is a new feature length documentary in production with a release date of 2011 that tells the political history of myalgic encephalomyelitis. You can help get the movie completed.
Myalgic Encephalomyelitis: The shocking disease
Jodi Bassett writes about the many ways getting myalgic encephalomyelitis is a ‘shock to the system’ of sufferers.
Mayo Clinic to Study CFS/FMS Amygdala Retraining
The Mayo Clinic is conducting a pilot study of the Gupta Amygdala Retraining™ Programme for patients with chronic fatigue syndrome (CFS) and fibromyalgia (FMS).
We, Tuskegee?
Severe ME/CFS/MCS patient Peggy Munson was hospitalized, near death, after the Ice Storm of December 11, 2008 and ensuing 3-day power outage. She remembers today, one year later.