ME/CFS Information Sites
Open Medicine Foundation
Our mission, at the Open Medicine Foundation, is to fund and initiate collaborative and groundbreaking research into chronic complex diseases so that patients will be able to live life more fully. Led by our esteemed ME/CFS Scientific Advisory Board, we’re now focused on the End ME/CFS Project, designed to find biomarkers and effective treatments for myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS).
"Health Rising is dedicated to providing timely, accurate information to people with chronic fatigue syndrome (ME/CFS) and fibromyalgia."
"Since becoming a non-profit, Phoenix Rising has worked to build its organizational capacity, to continue to provide the ME/CFS community with accurate, objective, up to date information, and to produce internet projects that will help patients find better practitioners, help them choose better treatments, and empower the community."
"A range of tools for proactive health management at your fingertips: comprehensive nutritional support for any number of health concerns, updates on the latest medical news, chat rooms, message boards and support communities with thousands sharing information, advice and treatment experiences."
The ME and CFS Information Page
Mary M. Schweitzer, Ph.D.
National ME / FM Action
"The National ME/FM Action Network became a Canadian charitable organization on June 18, 1993 dedicated to Myalgic Encephalomyelitis, also known as Chronic Fatigue Syndrome (ME/CFS) and Fibromyalgia (FM) through support, advocacy, education and research."
"We are an international network of patients fighting for health equality for Myalgic Encephalomyelitis (ME) and Chronic Fatigue Syndrome (CFS). We build community and mobilize patients, family, and allies to make ME visible and fight for health equality. We were founded with the belief that while we may find it difficult to advocate for ourselves in the physical world, by making our activism accessible, we can be an unstoppable force.."