Many ME/CFS scams of this nature have come and gone over the years. It always boils down to the scammer claiming he/she has a high accuracy diagnostic test or a potent treatment/cure, always presented in a fuzzy-on-the-details manner while presenting himself as a rebellious lone wolf scientist...
Pretty funny study if not for the fact that it will be used as a weapon against ME/CFS patients. These marginal associations don’t exceed the ambient noise / crud factor that afflicts this sort of questionnaire research and can easily be explained by the common method bias. They measured...
The problem with this study, like with most studies of this type (epidemiological trawling through EHR), is that the definition of outcome is quite crude. Everyone here probably has brain fog but how many doctors will actually put down something so serious on your record:
Most ppl complaining...
Not surprised to see this. We’ve seen other LP advocates who claim to have been cured drop out of mainstream employment and become public spokespeople for the alleged cure.
It’s really scary and demoralising seeing GET vultures getting their claws into another patient group. No amount of debunking of bad research seems to stop the BPS juggernaut. They just use a different name for the same illness and continue as if nothing has happened.
Agreed. It’s also telling that they deliberately chose not to do what most trials these days do which is to obtain written consent for data sharing.
Not that it’s even necessary to reanalyse the original dataset in this case. Unlike in PACE where the data analyses were fraudulent, here it’s...
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