see https://www.s4me.info/threads/action-for-me-has-joined-s4me.2944/ something to also think about is AfME is closely aligned to BACME....
link: https://www.sciencedirect.com/science/article/abs/pii/S002239992100057X (not on sci-hub yet)
I don't think they are singing Kumbaya anymore. or the joke about someone going up to heaven and seeing a large wall and asking 'who's behind...
10% of £35,000 target raised so far.
I would not have relied on Cochranes searches one bit given the way they were done for their exercise reviews and the poor upkeep of the Cochrane...
yes, but it continues asking questions about employment afterwards.
I thought the same thing; the Cochrane reviews on the MMR vaccine might be one to look at (I tried but my brains just not functioning right now);...
Long covid: let’s learn from profession’s record with CFS/ME patients...
[MEDIA]
I am an unsalaried research fellow who relies on grant income. I am seeking funding to continue researching Myalgic Encephalomyelitis/Chronic...
the problem is worse than that as it also applies to a lot of the so-called CFS/ME 'experts'.
yes well it took the Lancet 12 years to retract the Wakefield paper (2010), which btw is not mentioned by Cochrane in their systematic review of...
a lot of cbtwatch stuff here:...
I must be reading this differently to other people. this seems more like ECs current attempt to seem a bit more bio than psychosocial eg...
found a few interesting posts on EC on Mumsnet. Although some are quite old (eg 2009) it was the first time I'd seen that she indirectly 'charged'...
https://www.s4me.info/threads/government-and-insurance-companies-establishing-the-bps-model.2319/page-2#post-84353
Moved posts TOKYO -- Discrimination, prejudice and a lack of understanding about diseases sometimes causes patients more suffering than the...
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