King's researcher receives NIHR funding to study Long COVID "For more information, please contact Patrick O'Brien (Senior Media Office)"...
Paisley scientists lead groundbreaking research into long covid " Paisley academics are to lead groundbreaking research into the impact long covid...
the irony is that 'Adaptive Pacing Therapy' was the PACE authors version of 'pacing' which in the end they said was not as effective as CBT or GET...
Scotland: UWS project merged thread full article...
Survey – Do GPs in Wales use NICE guidance? People with ME are looking forward to the publication of the revised NICE guidance, expected on 18th...
moved post well worth a watch; this Dr Campbell has a lot of followers and seems to talk a lot of sense. Judging by the comments though( a lot of...
https://www.s4me.info/threads/paul-garner-on-long-covid-and-me-cfs-bmj-articles-and-other-media.15629/page-64#post-338423 eta: it appears PG is...
A major new consortium involving the University of Exeter, has been awarded £6.8 million by the National Institute of Health Research (NIHR) to...
The National Institute of Nursing Research (NINR), at the National Institutes of Health (NIH) is seeking people who are cancer survivors or have a...
[MEDIA] how indeed.
" Doctors with M.E. Honorary Fellow, Professor Derek Pheby, has responded to Dr. Nina Muirhead’s article for the Royal College of Physicians,...
The effect of IL-2 stimulation and treatment of TRPM3 on channel co-localisation with PIP2 and NK cell function in myalgic...
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a disease with unknown etiology, no validated specific and sensitive biomarker, and...
Invest in ME Research has won a £1,000 Movement for Good award thanks to nominations from the public....
"In this series, I dig a little deeper into the meaning of psychology-related terms… but not this week. Instead, we’ll take a look at ME/CFS, and...
seems to have started as a facebook group (75 members) https://www.facebook.com/groups/128056252168684/
except in many ways they aren't. What really irks is that it is obvious that they must have looked at ME/CFS research and literature , most of...
So that makes even less sense! Why not just call it 'Living with ME/CFS' in all three languages......talk about 'complex' :laugh: HHSH
Having watched the documentary in this thread...
Not saying the title should have been just 'living with ME' instead; maybe something more ambiguous to 'appeal' to all and more likely to be...
Separate names with a comma.
