Canadian registered charitable organization dedicated to advancing the recognition and understanding of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and Fibromyalgia through education, advocacy, support, and research.
The National ME/FM Action Network spearheaded the drive for the development of clinical definitions and guidelines and was responsible for the well known "Canadian case definition for ME/CFS"
The goals of the Foundation are to help fund medical research to expedite a treatment and eventual cure, to provide information, education, and support to those people who have Chronic Fatigue Immune Dysfunction (CFIDS) -- also known as Myalgic Encephalopathy (ME) and Chronic Fatigue Syndrome (CFS) and related illnesses such as Gulf War Illness.
Forum providing CFS and FM patients, caregivers and advocates access to comprehensive information and available resources
The New Jersey CFS Association is a not-for-profit, tax exempt organization whose purpose is to support patients, disseminate reliable information, and promote research.
For members, the organization has a large library of books on CFS which you can lend for a small price.
The primary aim of MERGE is to identify, commission and fund scientific investigations into the causes, consequences, and treatment of ME/CFS. It also aims to supply good-quality information, and to facilitate social care provision
Phoenix Rising provides comprehensive information on ME/CFS research and treatment as well as interviews with leading figures in the field.
The Research section provides brought extensive overviews of many important research areas in chronic fatigue syndrome including XMRV, Pathogens, Orthostatic Intolerance, the Brain, the Heart, RNase L. and more
The Whittemore Peterson Institute for Neuro Immune Disease exists to bring discovery, knowledge, and effective treatments to patients with illnesses that are caused by acquired dysregulation of both the immune system and the nervous system, often resulting in life long disease and disability.
