ME-CFSCommunity.com
Helping those affected by ME/CFS, FM and other neuroendocrine-immune disorders on their respective paths towards wellness.
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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).
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information | commentary | archives on the political issues affecting ME patients, advocates and carers
Medical news and health news headlines posted throughout the day, every day
Chronic Fatigue Syndrome, Fibromyalgia, and IC Disease
A Community for People With Myalgic Encephalomyelitis / Chronic Fatigue Syndrome
Der Fatigatio e.V. ist eine deutsche Patientenorganisation für Menschen, die an Myalgischer Enzephalomyelitis / Chronisches Fatigue Syndrom erkrankt sind.
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?
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
enlander.com by Liam Alexander is the ultimate source of tech, health and wellness tips, tricks and reviews. Find in-depth and comprehensive guides!
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
IACFS/ME is dedicated to the research of people affected by myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS), fibromyalgia, and other related conditions.
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
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
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)
A charity offering support to local people with ME, Fibromyalgia and Long Covid, and raising awareness of these chronic, debilitating illnesses.
Simmaron Research plays a key role in developing scientific research to improve diagnosis, treatment and medical understanding of ME/CFS and other neuroimmune diseases.
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and my hidden life.
Individuals Blogging For ME/CFS Awareness Every May
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