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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 »
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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 »
The lived experience of Severe ME
Watching Wall-E with the younglings. Who else feels like one these peeps? ヽ༼ຈل͜ຈ༽ﾉ 
What If You Never Get Better From Covid-19? 
Slow PEM Onset? Feedback 
Anyone else get really bad tremors? 
Symptoms change when moving between climates? (South/North Carolina) 
Weekly Inspiration: Winter Boosts 
Severe ME More Notes for Carers now available as a paperback on Amazon 
Jan. 22, 2021 fibromyalgia and Lyme news 
Large Long COVID Study and Major Media Articles Underscores Link to ME/CFS – Plus Countdown for the NIH 
ANNOUNCING THE PUBLICATION OF SEVERE ME: MORE NOTES FOR CARERS 
Guardian: The NHS must learn from its mistakes with other post-viral conditions such as ME/CFS – more research is vital 
TV Tuesday: Home Before Dark 
Movie Monday: The Peanut Butter Falcon 
Parliamentary debate on Long-Covid: What should be learned from ME/CFS? 
ME Awareness Week: let’s celebrate as a community but keep it smart – and apart! 
‘Full-up’ signs in place as medical students let us unpack the mysteries of ME/CFS 
A lockdown quiz took Ja to this extreme cycling challenge 
Potential fibromyalgia drug hits pain-relieving goal in clinical trial 
Favorite Movies Watched in 2020 
Top 10 Live with ME/CFS Blog Posts of 2020 
Thanks for Making Health Rising’s Year End Donation Drive a Success! 
ME/CFS and FM Experts on Whether to Take the Coronavirus Vaccine – Plus The Vaccine Polls 
Paradigm Shift for Long COVID (and ME/CFS?) Plus the Friendly Fire Hypothesis: Could Autoimmunity Explain long COVID? 
Ivabradine – Could a “Wonder Drug” For POTS Work in ME/CFS?