TiredSam
Committee Member
So now they hold us in such contempt that they can't even be bothered bullshitting any more?This information is not available.
How rude. Go on, at least take us seriously enough to bother making something up.
So now they hold us in such contempt that they can't even be bothered bullshitting any more?This information is not available.
I think it's the full and truthful answer that's spooked them ... so they plumped for an empty and not-very-truthful answer instead. The information has to be in data that must surely be available - criminal if such data not recorded. And querying the information out of that data is hardly an intractable problem. So they are afraid to make the answer available, which I'm sure the Countess of Mar was very aware of when asking the question.It's the word recovery that's confused 'em. So many definitions to choose from.
https://www.parliament.uk/business/...s/written-question/Commons/2018-05-14/143805/
Alex Chalk
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to stimulate and facilitate high-quality research into chronic fatigue syndrome.
I wonder how they decide on "the importance of the topic to patients and health and care services, value for money and scientific quality".Reply received and Alex notified us (3 who met him together) by email this afternoon.
Answered by: Caroline Dinenage Answered on: 22 May 2018
The Department National Institute for Health Research (NIHR) recognises that chronic fatigue syndrome (CFS), also known as myalgic encephalomyelitis (ME), is a debilitating condition. The NIHR is speaking with the United Kingdom’s CFS/ME Research Collaborative and patient representatives about how best we can support a joined up approach to high quality research into this complex disorder. The NIHR welcomes funding applications for research into any aspect of human health, including CFS/ME; it is not usual practice to ring-fence funds for particular topics or conditions. Applications are subject to peer review and judged in open competition, with awards being made on the basis of the importance of the topic to patients and health and care services, value for money and scientific quality
Full
https://www.parliament.uk/business/publications/written-questions-answers-statements/written-questions-answers/?page=1&max=20&questiontype=AllQuestions&house=commons,lords&use-dates=True&answered-from=2018-05-14&answered-to=2018-05-22&member=4481&dept=17&keywords=cfs
Caroline Dinenage Minister of State (Department of Health and Social Care)
In the period in question, the major National Institute for Health Research (NIHR) funding for biomedical research was through its Biomedical Research Centres and Units. These support research funded by the NIHR itself and also research funded by other public, charity and industry research funders. The level of funding for biomedical research into chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) for each financial year can be found in the table below. The funding for this research came from a combination of funders.
Financial Year
£
2014-15
280,442
2015-16
295,626
2016-17
130,958
The NIHR Clinical Research Network (CRN) provides the infrastructure that allows high-quality clinical research funded by charities, research funders and life-sciences industry to be undertaken throughout the National Health Service. The level of funding for biomedical research into CFS/ME for each financial year can be found in the table below. The funding for this research came from a combination of the NIHR, the Medical Research Council (MRC) and medical research charities. Expenditure from the CRN coordinating centre itself is also outlined below:
Financial Year
CRN funding for research, £
Coordinating expenditure, £
2014-15
134,769
17,485
2015-16
125,176
17,796
2016-17
82,866
7,821
The MRC spend on research directly relating to CFS/ME can be found in the following table. Research into CFS/ME is a continuing priority for the MRC.
Financial Year
£
2014-15
652,044
2015-16
287,234
2016-17
286,197
The NIHR and the MRC welcomes funding applications for research into any aspect of human health, including biomedical research into CFS/ME. It is not usual practice to ring-fence funds for particular topics or conditions. Applications are subject to peer review and judged in open competition, with awards being made on the basis of the importance of the topic to patients and health and care services, value for money and scientific quality. On this basis, it is not possible to say how much funding is planned in the current financial year.
The NIHR recognises that CFS/ME is a debilitating condition and is speaking with the United Kingdom CFS/ME Research Collaborative and patient representatives about how best we can support a joined up approach to high quality research into this complex disorder.
https://www.parliament.uk/business/...s/written-question/Commons/2018-05-17/145357/@Sly Saint, can you give the link to the reply you've just posted, I can't find it.
Yeah, I'd agree. I call bullshit on those figures, I bet most of them are behavioural research.eta: am not sure if all of this is 'biomedical' as we understand it(?)
Perhaps it would be helpful to see how many people are off work sick with the different conditions?Perhaps some of you remember the bubbles video for 2011. I did do an update for 2017. Here are the final scenes: you will be truly stunned by the difference.
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What's the betting someone says behavioural research is biomedical research and starts blabbering on about cartesian dualism?Yeah, I'd agree. I call bullshit on those figures, I bet most of them are behavioural research.