I assumed the figure was a joke.
I can't say I've seen such a thing, except Crawley's LP trial and Magenta. Ultimately, it's up to the ethics committee to stop such inappropriate...
She is an author on the Magenta paper.
Same here. Transitioning from moderate (flu-like malaise PEM) to severe (extreme dysautonomia) was a terrifying experience. It occurred rather...
Yep. Lay members of the public have no idea how difficult it is to prove research misconduct or to get journals to take action even when proven. I...
This section highlights how they think. ME/CFS is a diagnosis of exclusion and if some “real” disease is found in your body, you can’t also have...
It’s very surprising to see this trial so transparently reported. Perhaps the huge pushback on SMILE (and the whole debacle of having nearly the...
Most making a good or complete recovery? How are they able to get away with these shameless statements?
I'd like to know if they're still using GET (or whatever euphemism they're using these days to circumvent the NICE guidelines) in their clinical...
Going down this route will also allow them to focus on the stigmatising bit and give a lecture on dualism, ignoring the stronger and most...
People with very severe psychiatric disorders also have an inability to eat/drink or mobilise so it's very easy to dismiss severe ME/CFS as...
It's literally the same CBT formulation they use for anxiety disorders such as agoraphobia with panic attacks. They think nothing is wrong other...
So they stopped recruitment in 2018, had the results in 2019 (1-year follow-up) and have been sitting on them for 5 years, quietly offloading them...
Crawley in her 2016 letter makes several audacious statements about lack of any side effects: The letter sounds even more sinister in hindsight...
It takes very little to harm people with GET. There have been anecdotal reports of people who went from moderate to severe after just one session.
They're going to have a hard time spinning this as GET and activity management being "equally effective" since neither was effective and the...
It's the go-to website for neurologists when confronted with patients whose symptoms they can't explain. Lots of reports on social media of being...
Reaching out to Treadway is a good idea as long as the letter is laser focused on the misinterpretation of the EEfRT task, not the wider ME/CFS...
Government and insurance industry trying to minimise long-term disability payments by denying that the illness exists. It really is as simple as that.
Nothing to do with the journal. As an author, you can choose whether to make your paper open access or not. Keeping your paper behind a paywall is...
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