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Cort Johnson founded Phoenix Rising and Health Rising to support people with chronic fatigue »
Helping to make the UK a better place for people with ME/CFS. ME/CFS is hard to accept. And those »
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome / ME / SEID. »
I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since March 2002.Both of »
A community blog for nutrition, chronic fatigue syndrome and fibromyalgia highlighting symptoms, »
A bit about me, I guess. Where to start. I work two jobs at the moment, both part time, anywhere »
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This is too true 
Advice Needed: Husband and daughter and resentment 
Hard to remember that my memory isn't good 
When I've finally done the dishes and anyone (even me) makes a sandwich or a cup of tea 
The ME Association End of Week Research Round-up | 14 February 2020 
What do you think good healthcare for M.E. should look like in Scotland? | 14 February 2020 
Share Your Stories for ME Awareness Week: The Lost Years and a Focus on Symptoms| 13 February 2020 
Childhood ME/CFS Prevalence Take a Hike – Plus Take the Childhood Poll 
Now Available! Finding a New Normal: Living Your Best Life with Chronic Illness. 
TV Tuesday: Lincoln Rhyme: Hunt for the Bone Collector 
First ME/CFS Pediatric Population Study Published 
Weekly Inspiration: When Difficult Times Hit 
Weekly Inspiration: Rediscovering Mercy 
Nutrition 101: Sugar, Fodder for the Fire 
My 7 year anniversary 
MEA Summary Review: Assessing diagnostic value of microRNAs from PMBC’s and EV’s in ME/CFS | 11 February 2020 
Coronavirus infection and ME/CFS | 11 February 2020 
Bridging the Gap? Fibromyalgia, Women and Autoimmunity 
“Left Out”: A Movie of Commitment, Hope, Despair and Rituximab 
Building It! An ME/CFS/FM Community: An Exploratory Survey 
“Crushing It”: Large Pridgen Fibromyalgia Antiviral Trial Expected This Summer 
The fear of stopping 
Letting others help