Information about Myalgic Encephalomyelitis
World Health Organisation definition- "Myalgic Encephalomyelitis (M.E.) is a debilitating neurological disease which has been recognised by the World Health Organisation (WHO) since 1969 as a distinct organic neurological disorder. M.E. is classified in the current WHO International Classification of Diseases with the neurological code G.93.3."
Video about M.E., Voices From The Shadows
The Nightingale Research Foundation- The Nightingale Research Foundation is a Canadian registered charitable organization dedicated to the study and treatment of Myalgic Encephalomyelitis (M.E.) and Chronic Fatigue Syndrome (CFS) and related illnesses. We have been investigating M.E. and CFS patients since 1984. These thousands of case studies have formed the basis of our research into the causes and treatment for symptoms, and have led to a continual enhancement of our diagnostic protocols. We are now integrating the knowledge gained from this case-based research as we re-define the disease “of a thousand names”. Continue reading...
The Hummingbirds' Foundation for M.E.- Most websites and groups which deal with these topics are heavily influenced by the misinformation promoted by vested interest groups. They are unreliable, of poor quality and do not serve patients' interests.
Patients with M.E. and all those diagnosed with 'CFS' that do not have M.E. have gotten a raw deal for the last 20 years. Continue reading...
Dr Jamie Deckhoff-Jones's blog
Video about M.E., Voices From The Shadows
The Nightingale Research Foundation- The Nightingale Research Foundation is a Canadian registered charitable organization dedicated to the study and treatment of Myalgic Encephalomyelitis (M.E.) and Chronic Fatigue Syndrome (CFS) and related illnesses. We have been investigating M.E. and CFS patients since 1984. These thousands of case studies have formed the basis of our research into the causes and treatment for symptoms, and have led to a continual enhancement of our diagnostic protocols. We are now integrating the knowledge gained from this case-based research as we re-define the disease “of a thousand names”. Continue reading...
The Hummingbirds' Foundation for M.E.- Most websites and groups which deal with these topics are heavily influenced by the misinformation promoted by vested interest groups. They are unreliable, of poor quality and do not serve patients' interests.
Patients with M.E. and all those diagnosed with 'CFS' that do not have M.E. have gotten a raw deal for the last 20 years. Continue reading...
Dr Jamie Deckhoff-Jones's blog