This week we learned that online activists are silencing scientists in the UK: Reuters contacted a dozen professors, doctors and researchers with experience of analysing or testing potential treatments for chronic fatigue syndrome. All said they had been the target of online harassment because activists objected to their findings. Only […]
Great news. The PACE Trial controversy has been resolved! Oh, wait…er, no it hasn’t. Rather, the spin cycle of eminence-based medicine continues. The UK’s Health Research Authority have released a report on their assessment of the beleaguered PACE Trial, and have concluded that they are happy with it. Cue the […]
I am behind on posting it, but here we go. This video has already attracted a staggering number of worldwide views, but I thought I would (should) present it here for posterity. Kudos to everyone at the charity Hope 4 ME & Fibro NI who organised the event (back in […]
Lines are drawn A quarter of a million Britons are believed to have myalgic encephalomyelitis (ME), the condition that sometimes overlaps with chronic fatigue syndrome (CFS). ME/CFS is a severe debilitating illness that renders patients either temporarily or perennially immobile. Sufferers will have often led very active lives before being […]
And I’m one of them. This is important not least because of claims appearing over the weekend that Cochrane pulled its controversial review due to pressure from brain-addled trouble-making “patient activitists,” rather than for scientific reasons. Claims that Cochrane had been harassed were made not by Cochrane themselves, but, rather, […]
