The MEAction Network

#MEAction (The Myalgic Encephalomyelitis Action Network) is an ME/CFS patient advocacy group co-founded May 12, 2015 by Jennifer Brea and Beth Mazur.

It is a global organization whose focus is on empower patients to take action to improve the research and treatment situation. #MEAction runs special interest groups focused on science & research, public education and press relations.

MEpedia was launched by MEAction.

Online presence

• MEAction.net #MEActon website
• @MEActNet - Twitter
• fb.com/meatcnet - Facebook

myalgic encephalomyelitis (M.E.) - A disease often marked by neurological symptoms, but fatigue is sometimes a symptom as well. Some diagnostic criteria distinguish it from chronic fatigue syndrome, while other diagnostic criteria consider it to be a synonym for chronic fatigue syndrome. A defining characteristic of ME is post-exertional malaise (PEM), or post-exertional neuroimmune exhaustion (PENE), which is a notable exacerbation of symptoms brought on by small exertions. PEM can last for days or weeks. Symptoms can include cognitive impairments, muscle pain (myalgia), trouble remaining upright (orthostatic intolerance), sleep abnormalities, and gastro-intestinal impairments, among others. An estimated 25% of those suffering from ME are housebound or bedbound. The World Health Organization (WHO) classifies ME as a neurological disease.

PACE trial A controversial study which claimed that CBT and GET were effective in treating "CFS/ME", despite the fact that its own data did not support this conclusion. Its results and methodology were widely disputed by patients, scientists, and the peer-reviewed scientific literature.