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Cort Johnson founded Phoenix Rising and Health Rising to support people with chronic fatigue » Cort Johnson founded Phoenix Rising and Health Rising to support people with chronic fatigue syndrome and fibromyalgia. Health Rising provides the latest treatment and research information for people with fibromyalgia and chronic fatigue syndrome. Follow to get frequent and up-to-date information.

Helping to make the UK a better place for people with ME/CFS. ME/CFS is hard to accept. And those » Helping to make the UK a better place for people with ME/CFS. ME/CFS is hard to accept. And those who do not accept their illness rarely recover. So we help people understand and come to terms with their illness.

The aims of ME Research UK are to advance scientific knowledge by funding biomedical research » The aims of ME Research UK are to advance scientific knowledge by funding biomedical research into the causes, consequences and treatment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), and to provide high quality information on all aspects of the disease for a wide range of audiences. Follow to get information on all researches on CFS/ME.

Our Current Focus The Open Medicine Foundation is spearheading research into ME/CFS and related » Our Current Focus The Open Medicine Foundation is spearheading research into ME/CFS and related chronic complex diseases that follow patterns of success and benefits from collaborating with leading scientists and clinicians from around the globe. The current focus is on ME/CFS, with the expectation that discoveries in this disease will bring answers to other similar chronic complex diseases. Follow and get updates on researches on ME/CFS and other chronic diseases.

Medical Advancement Treatment ME/CFS and Fibromyalgia. Bateman Horne Center - Empowering Patients » Medical Advancement Treatment ME/CFS and Fibromyalgia. Bateman Horne Center - Empowering Patients, Advancing Research and Improving Care for all those with ME/CFS and Fibromyalgia. Follow this blog and get researches on eradicating ME/CFS & Fibromyalgia.

I am Suzan Jackson. I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since » I am Suzan Jackson. I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since March 2002. Both of my sons also got ME/CFS at ages 6 and 10. This blog is about how our family lives with chronic illness, with a focus on living and enjoying our lives in spite of these challenges.

This is about me and M.E. (Myalgic Encephalomyelitis). It`s about living with a chronic and » This is about me and M.E. (Myalgic Encephalomyelitis). It`s about living with a chronic and invisible illness. It`s how I express that life through my poetry.

Covers articles about living with Severe ME/CFS - advice, resources and inspiration for patients » Covers articles about living with Severe ME/CFS - advice, resources and inspiration for patients, caregivers, doctors and supporters, by Whitney Dafoe.