This is a list of notable people who have been diagnosed with or suspected to have myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).
Name | Occupation | Nationality |
---|---|---|
Michelle Akers [1] | Former Olympic soccer player | American |
Karin Alvtegen [2] | Author | Swedish |
Paul Atherton [3] | Television and film producer | British |
Elisabeth Tova Bailey [4] | Author | American |
Ann Bannon [5] | Author | American |
Richie Barnett [6] | Rugby League player and television presenter | New Zealander |
Henrik Berggren [7] | Lead singer in the band Broder Daniel | Swedish |
Emma Blackery [1] | YouTuber and singer-songwriter | British |
Susan Blackmore [1] | Writer and lecturer | British |
Howard Bloom [1] | Publicist and writer | American |
Olaf Bodden [8] | Professional soccer player | German |
Jennifer Brea [9] | Documentary filmmaker and activist | American |
Ricky Carmichael [10] | Motocross racer | American |
Cher [1] [11] | Recording artist, actress, director, and record producer | American |
Roger Cicero [12] | Jazz and pop musician | German |
Pema Chödrön [13] | Buddhist nun | American |
Susanna Clarke [14] | Author | British |
Tom Clarke [15] | Politician | British |
Neil Codling [16] | Keyboard player for the band Suede | British |
Dianna Cowern [17] | YouTuber and science communicator | American |
Merryn Crofts | Drama student whose death was caused by ME/CFS [18] | British |
Michael Crawford | Actor and singer | British |
Mia Diekow [19] | Musician, voice actress, patient advocate | German |
Laura Dundovic [20] | Former Miss Universe Australia | Australian |
Blake Edwards [1] [21] | Film director, screenwriter and producer | American |
Florian-Ayala Fauna [22] [23] | Artist, musician, music producer | American |
Flea (Michael Balzary) [24] | Bassist of the Red Hot Chili Peppers | Australian-American |
Clare Francis [25] | Yachtswoman and novelist | British |
Luke Ford [26] | Journalist and Blogger | Australian-American |
Leigh Hatcher [27] | Journalist and news presenter | Australian |
Susan Harris [28] | Television writer and producer | American |
Jens Höing [29] | Racing driver | German |
Laura Hillenbrand [1] [30] | Author | American |
Andy Hunt [1] [31] | Association footballer | British |
Keith Jarrett [1] | Jazz pianist | American |
Leonard A. Jason [32] | Professor of psychology at DePaul University | American |
Stephan Jenkins [33] | Lead singer of Third Eye Blind | American |
Brynmor John [34] [35] [36] | Politician | British |
Roger King [37] | Novelist | British living in US |
Trip Lee | Rapper | American |
Peter Marshall [38] | Squash player | British |
Brooks Mileson [39] | Businessman | British |
Sophia Mirza [40] | A woman who was the first to have CFS listed as a cause of death in the UK [40] | British |
Stuart Murdoch [41] | Musician, lead singer in the band Belle and Sebastian | British (Scottish) |
Stevie Nicks [42] | American singer-songwriter | American |
Andrew Oldcorn [43] | Golfer | British |
Amy Peterson [1] | Short track speed skater | American |
Martin Phillips [31] | Association footballer | British |
David Puttnam [44] | British film maker and producer | British |
John Rutter [45] | Composer | British |
Ali Smith [1] [46] | Author | British |
Casey Stoner | MotoGP world champion | Australian |
Amy Studt | Musician | British |
Ari Taub | Olympic Greco-Roman wrestler | Canadian |
Marina Weisband [47] | Politician | German |
Naomi Weisstein [48] | Author and neuroscientist | American |
Ken Wilber [49] | Author | American |
Chris Willsher [1] | Singer with The Bus Station Loonies | British |
Katharine Windsor [50] | Duchess of Kent | British |
Yvette Cooper [51] [52] | Politician | British |
Name | Occupation | Nationality |
---|---|---|
Charles Darwin [53] | Naturalist, geologist, and biologist | British |
Florence Nightingale [53] | Founder of modern nursing | British |
The ME Association is a UK health charitable organization that provides information, advocacy, and services to persons and families affected by ME/CFS, and raises funds for research into ME/CFS. It has been reported to be one of the two largest UK charities for ME/CFS.
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) has a long history with an evolution in medical understanding, diagnoses and social perceptions.
Management of ME/CFS focuses on symptoms management, as no treatments that address the root cause of the illness are available. Pacing, or regulating one's activities to avoid triggering worse symptoms, is the most common management strategy for post-exertional malaise. Clinical management varies widely, with many patients receiving combinations of therapies. The prognosis of ME/CFS is poor, with recovery considered “rare”.
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is an illness with a history of controversy. Although it is classified as an organic disease by a majority of researchers, it was historically assumed to be psychosocial, an opinion still held among many physicians. The pathophysiology of ME/CFS remains unclear, there exist many competing diagnostic criteria, and some proposed treatments are controversial. There is a lack of education and accurate information about the condition among a significant number of medical practitioners, which has led to substantiated accusations of patient neglect and harm.
Clinical descriptions of ME/CFS vary. Different groups have produced sets of diagnostic criteria that share many similarities. The biggest differences between criteria are whether post-exertional malaise (PEM) is required, and the number of symptoms needed.
The Lightning Process (LP) is a three-day personal training programme developed and trademarked by British osteopath Phil Parker. It makes unsubstantiated claims to be beneficial for various conditions, including ME/CFS, depression and chronic pain.
Graded exercise therapy (GET) is a programme of physical activity that starts very slowly and gradually increases over time, intended as a treatment for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Most public health bodies, including the CDC and NICE, consider it ineffective, and its safety is disputed. However, GET still enjoys support among a minority of clinicians and organizations.
David Sheffield Bell is an American physician who has done extensive research on the clinical aspects of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). He has also conducted evaluations and research in pediatric ME/CFS and written numerous articles about the condition.
Daniel Peterson is an American physician in private practice in the state of Nevada, and has been described as a "pioneer" in the treatment of Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). He graduated from the University of Rochester School of Medicine, Rochester, New York, in 1976 and was an intern and resident at the University of Utah Medical Center from 1976 to 1979. In 1979, he became a diplomate of the American Board of Internal Medicine. He is president of Sierra Internal Medicine of Incline Village, established in 1981.
The Chronic Fatigue Syndrome Advisory Committee (CFSAC) was formed in response to the use of funds by the United States Centers for Disease Control and Prevention in the study of chronic fatigue syndrome (CFS). The CFSAC was charted under the Public Health Service Act of the US and funded by the United States Department of Health and Human Services (HHS). The CFSAC advises the Secretary of Health and Human Services on issues related to its mandate, including issues related to access and care for individuals with CFS, research, public health, clinical care and education regarding CFS. In November, 2008, support for CFSAC activities was changed to the Office on Women's Health, a division of the Office of Public Health and Science. It held it first meeting in 2003.
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a disabling chronic illness. People with ME/CFS experience profound fatigue that does not go away with rest, as well as sleep issues and problems with memory or concentration. The hallmark symptom is post-exertional malaise, a worsening of the illness which can start immediately or hours to days after even minor physical or mental activity. This "crash" can last from hours or days to several months. Further common symptoms include dizziness or faintness when upright and pain.
Jennifer Brea is an American documentary filmmaker and activist. Her debut feature, Unrest, premiered at the 2017 Sundance Film Festival and received the US Documentary Special Jury Award For Editing. Brea also co-created a virtual reality film which premiered at the Tribeca Film Festival.
Rosamund Vallings is a medical doctor, known as one of the leading authorities on Chronic Fatigue Syndrome (ME/CFS) in New Zealand.
Post-exertional malaise (PEM), sometimes referred to as post-exertional symptom exacerbation (PESE) or post-exertional neuroimmune exhaustion (PENE), is a worsening of symptoms that occurs after minimal exertion. It is the hallmark symptom of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and common in long COVID and fibromyalgia. PEM is often severe enough to be disabling, and is triggered by ordinary activities that healthy people tolerate. Typically, it begins 12–48 hours after the activity that triggers it, and lasts for days, but this is highly variable and may persist much longer. Management of PEM is symptom-based, and patients are recommended to pace their activities to avoid triggering PEM.
International May 12th Awareness Day, also known as International ME/CFS Awareness Day is held every year to raise awareness of myalgic encephalomyelitis/chronic fatigue syndrome, fibromyalgia, multiple chemical sensitivity, Gulf War syndrome and other chronic immunological and neurological diseases (CIND).
Idiopathic chronic fatigue (ICF) or chronic idiopathic fatigue or insufficient/idiopathic fatigue is a term used for cases of unexplained fatigue that have lasted at least six consecutive months and which do not meet the criteria for myalgic encephalomyelitis/chronic fatigue syndrome. Such fatigue is widely understood to have a profound effect on the lives of patients who experience it.
DecodeME is an ongoing genome-wide association study searching for genetic risk factors for Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). With a planned recruitment of 25,000 patients, it is expected to be the largest such study to date. Recruitment closed on 15 November 2023 and results are expected in 2025.
The Open Medicine Foundation (OMF) is a US-based charity that funds research into the illnesses myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), fibromyalgia, post-treatment Lyme disease syndrome, and long COVID.
A 2-day CPET is a cardiopulmonary exercise test given on two successive days to measure the effect of post-exertional malaise (PEM) on a patient's ability to exercise. PEM is a cardinal symptom of myalgic encephalomyelitis/chronic fatigue syndrome and is common in long COVID as well.
The PACE trial was a large and controversial trial which compared the effects of cognitive behavioural therapy (CBT), graded exercise therapy (GET), adaptive pacing therapy, and specialist medical care for people with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).