Very good article by Mark Vink, MD & Vink-Niese. Explains why NICE is right to recommend against graded exercise & CBT as treatments for ME/CFS. Also cautions against repeating mistakes that have been made with ME/CFS in #LongCovid research & treatment: journals.sagepub.com/doi/full/10.11…

Cake and inner calm: 10 ways to improve your mood – without exercising theguardian.com/lifeandstyle/2…

The hierarchy of disagreement from "How to Disagree" by Paul Graham.

Apparently just by talking about #longCovid can spread the illness "Press coverage.. as well as the work of support groups and sympathetic doctors, could induce people to believe they had [long Covid], thereby spreading it."  #MECFS #pwME theguardian.com/commentisfree/…

The National Institute for Health And Care Excellence published its analysis of the Pace trial findings and now advises "doctors not to promote CBT or GET as treatments or cures for #MECFS" #pwME #SickNotTired theguardian.com/commentisfree/…

Daniel Missailidis swept up the People's Choice Award at the 7News YAA’s and we’re ecstatic! A huge thank you to the community for helping make this a reality. We’re so glad to see Daniel being recognised for his work in the ME/CFS research field. Congratulations Daniel! #MECFS

Postdoctoral position open at Cornell-Ithaca NY for project on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Candidate should be able to perform analysis of existing datasets on metabolomics, proteomics, single cell genomics. Contact [email protected]

"#MEcfs can be triggered by COVID-19 in adolescents and young adults. Further work is needed to determine the pathogenesis of ME/CFS after COVID-19 and optimal methods of treating these patients." #pwme #longCOVID #MEresearch frontiersin.org/articles/10.33…

Nice to see the continued research support for #MECFS provided by the national #cfids foundation. An interesting hypothesis linking #MECFS and cancer

2 molecules involved in mitochondrial #metabolism, fumarate and isocitrate, help overcome anaemia caused by #chronicillness and #inflammation #inmice nature.com/articles/s4146…

It is vital that researchers and docs listen attentively when patients share their lived experience of illness. There is everything to gain and nothing to lose

Please see the link below to view the sample questionnaire. drive.google.com/file/d/1lb9F1G…

Check this out, a diagnostic questionnaire for the diagnosis of #MECFS Could be helpful for #pwME and doctors With over 80% of #pwME undiagnosed, there is an urgent need for better diagnostic tools #MedTwitter #MedEd

Here is my #MillionsMissing story. To make your own or see the gallery click here 12may.org 12may.org/poster/6095dc8… #mecfs #pwME #EmergeAustralia Emerge Australia

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Myalgic encephalomyelitis - hard to say, even harder to live with. #sayME #MECFSAwarenessWeek

Note 29 residential aged care facilities completely unvaccinated. Not a single dose

The complacency over hotel quarantine is scientifically and economically unsustainable. One leak and a state might be shut down.

"I felt I had wasted years of my life trying to convince health professionals of my physical symptoms." Sarah Clark shares what it is like to experience a misdiagnosis and how health professionals can support someone who has been misdiagnosed ow.ly/YnBH50EVRPe