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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.

I am Jennie Spotila, and I fell ill with Myalgic Encephalomyelitis on October 6, 1994. I am » I am Jennie Spotila, and I fell ill with Myalgic Encephalomyelitis on October 6, 1994. I am disabled, and mostly housebound, but I have been active in writing about ME/CFS and advocating for more research funding since the late 1990s. Follow me as I share my journey with ME/CFS.

FedUpwithFatigue.com brings you the latest news, research and useful tips to help you live better » FedUpwithFatigue.com brings you the latest news, research and useful tips to help you live better with fibromyalgia and/or Lyme. Follow me as I share tips to live better.

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.

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome / ME / SEID. » For research, treatments, and personal stories regarding Chronic Fatigue Syndrome / ME / SEID. Follow this reddit to get articles on all things related to ME/CFS.

Celebrating the ordinary while managing ME/CFS. Sharing practical advice, encouragement, faith » Celebrating the ordinary while managing ME/CFS. Sharing practical advice, encouragement, faith notes and raising awareness of invisible chronic illness. Staying hopeful despite Chronic Illness. navigating spoonie life. Sharing Faith, Crafts, practical advice and Encouragement.

I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since March 2002.Both of » 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.

I am a Christian, saved by grace alone through faith alone. I have had the neuroimmune disorder » I am a Christian, saved by grace alone through faith alone. I have had the neuroimmune disorder ME, Myalgic Encephalomyelitis, since 1991. From North Somerset, now in Northern Ireland. Please see my website for further information about ME.

A bit about me, I guess. Where to start. I work two jobs at the moment, both part time, anywhere » A bit about me, I guess. Where to start. I work two jobs at the moment, both part time, anywhere from 3 to 5 days a week of varying length. I play bass guitar, I'm currently in 1 band, a backup bassist to another band and always considering more musical projects.