Understanding Myalgic Encephalomyelitis Nightingale Press
This easy to read, hard cover, coloured, library quality 8.5 x 11-inch (22 x 28 cm) book with sewn pages is the best and most comprehensive book ever written on M.E. and CFS containing essential advice for patients and physicians.
Language: English
ProHealth Longevity creates high-quality anti-aging supplements backed by science. Browse products suited to your needs that encourage a long, healthy lifestyle.
ME/FM Action Network is a Canadian, registered, non-profit organization dedicated to advancing the recognition and understanding of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) and Fibromyalgia Syndrome (FMS) through education, advocacy, support, and research. Copyright 2020 National ME/FM Action Network
Up-to-date information about possible causes and treatments for Chronic Fatigue Syndrome, M.E., CFS and CFIDS; also examation of biochemical processes common to other multi-system illnesses. Detoxification, nutrition and holistic health
News Analysis With a Sense of Humor
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Simmaron Research plays a key role in developing scientific research to improve diagnosis, treatment and medical understanding of ME/CFS and other neuroimmune diseases.
Foggy Friends is a support and information website for sufferers of Myalgic Encephalomyelitis (ME), Chronic Fatigue Syndrome (CFS), Chronic Fatigue Immune Dysfunction Syndrome (CFIDS), Post Viral Fatigue Syndrome (PVFS) and Myalgic Encephalopathy (ME).
enlander.com by Liam Alexander is the ultimate source of tech, health and wellness tips, tricks and reviews. Find in-depth and comprehensive guides!
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IACFS/ME is dedicated to the research of people affected by myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS), fibromyalgia, and other related conditions.
A blog about ME/CFS and CFIDS recovery. (Chronic Fatigue Syndrome). Can we all heal from ME, CFS and Fibromyalgia and from its root causes?
A charity offering support to local people with ME, Fibromyalgia and Long Covid, and raising awareness of these chronic, debilitating illnesses.
The WWMEA provides support group meetings and information for those affected by CFS (chronic fatigue syndrome), M.E. (myalgic encephalomyelitis), CFIDS (chronic fatigue and immune dysfunction syndrome)
Der Fatigatio e.V. ist eine deutsche Patientenorganisation für Menschen, die an Myalgischer Enzephalomyelitis / Chronisches Fatigue Syndrom erkrankt sind.
Individuals Blogging For ME/CFS Awareness Every May
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and my hidden life.
Blue Ribbon for Awareness of ME; BRAME is an worldwide organisation to raise awareness of ME and CFS through support and information, run by Tanya Harrison and Christine Harrison
Myalgic Encephalomyelitis (M.E.) Advocacy
CFS Central reports breaking news, research and disputes on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and XMRV.
Helping those affected by ME/CFS, FM and other neuroendocrine-immune disorders on their respective paths towards wellness.
Information and research into chronic fatigue syndrome/myalgic encephalomyelitis (ME/CFS), chronic stress, burnout, the HPA axis, autonomic nervous system, the placebo effect and the relationship between stress load, mental attitude, lifestyle and physical health
Blogore is an info site that you can trust to always give you the most accurate and up-to-date information - from health and fitness to money and careers.
monitoring ICD-11, ICD-10-CM, DSM-5, SNOMED CT and other classification and terminology systems
Information about chronic fatigue syndrome, myalgic encephalomyelitis (ME/CFS) treatment and management. Improving care and advancing research towards a cure.