I'm hoping to get an overview of biomedical abnormalities found in ME/CFS that were replicated by multiple groups. I realize that, due to the paucity of research, most of the findings are unimportant and non-specific with some inconsistencies in the findings but I still think it would be useful...
A friend on mine (Evelien) has succeeded in getting a petition on ME accepted by the EU Parliament [link below*]. The petition highlights the impact of ME on 2 million people in the EU and the lack of EU funding for ME Research. I'd be grateful if you would consider supporting it (and ask...
Has anyone done a breakdown of funding between the two camps?
Ideally I'd like something for UK, and global:
BPS research $ per year, biomedical $ per year.
Clearly there would be some room for argument - for example a biomarker paper that mentions CBT as useful.
I feel a useful argument to...
I had not heard of this 'charity' before.
https://acmedsci.ac.uk/
Unfortunately Simon Wessely is also connected and frequently takes part in their events.
But, just maybe there are people who might be able to give a really 'independent' objective review of PACE and related issues? eg...
Editorial: UK life science research: time to burst the biomedical bubble
The precariousness of life science research in the UK can also be traced back to a lacklustre approach to research integrity. Research misconduct, questionable research practices, and a reliance on publication numbers as a...
I thought that in response to the Ministers statement at the debate on PACE yesterday that a break down of funding for research between psychological 'treatment' and actual biomedical research would also clearly show how skewed the research into ME is.
The only figures that have been collated...
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