This post and some of the following posts have been moved from this thread: NICE delay publication till 9 dec 2020. Draft guideline consultation...
Moderator note: Use this thread to discuss the possibility of an ME/CFS or ME/CFS-like illness following Covid-19. Initial posts have been moved...
Apologies if it has been posted before. I've heard about it, but haven't seen this official statement from Cochrane about it. It's not dated, but...
Back in 2018, the authors of a then-unpublished systematic review fired a spin- and error-laced salvo at the Cochrane review of the HPV vaccines....
Heathers is a data thug with @sTeamTraen [MEDIA] But when it comes to understanding scientific malfeasance, I think one bias that’s in the...
When I was 29 years old, I got so sick that I had to stop working. I had this intermittent burning pain in my legs, I woke up each morning with...
In my experience it can be difficult to get non-sufferers to properly engage with M.E. advocacy efforts. There can be many reasons for this....
http://cepuk.org/2020/02/08/guest-blog-nice-depression-guideline-cautious-optimism/?fbclid=IwAR1c2BN81TyQ79EjH8IYSjTeztHESk1i7rP3-GmiJJDLLH3HDrNlax...
Leonard Jason research finds that many young people have ME/CFS [ATTACH] A new study finds that 0.75%, or 1 in 130 young people, have ME.CFS....
https://sciencebasedmedicine.org/a-miracle-cancer-prevention-and-treatment-not-necessarily-as-the-analysis-of-26-articles-by-legendary-hans-eysenck...
For something so fundamental to the practice of science, it’s perplexing that it took so long for serious research into editorial peer review to...
It’s exactly ten years to the day since I started this blog. Oh my god, that’s a fucking long time to feel like shit every minute of every day....
Dear Father Christmas, I do apologise for bothering you. I know December is fiendishly busy, and how you manage to conjure such good cheer in it,...
No, of course, the systematic review/meta-analysis hasn’t died. But I kind of wish the flag-waving for the claim that its current form should die,...
Activism and new ways of getting input from a much wider range of patients and communities are needed to advance patient and public partnership in...
ME Association: “Get Well Soon” – Guest Blog by Louise Shepherd...
https://www.emerald.com/insight/content/doi/10.1108/S1479-354720190000011028/full/html Sick and Tired: Narratives of Contested Illness in...
Patient involvement in research—a brief history There is a well-described mismatch between the research that is done on a particular condition...
We’re Incentivizing Bad Science Current research trends resemble the early 21st century’s financial bubble ... Unless and until leadership is...
Saw this and it looks like a blog hosted on a newspaper platform. Pretty decent. Myalg. Encephalomyelitis ME is more widespread in Germany than...
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