Thanks for the mention of David Bell's work, @Denise and Snowdrop. It was interesting to read that thread in the context of Garner's assertions about normality.There's a thread here on his insight here:
Thanks for the mention of David Bell's work, @Denise and Snowdrop. It was interesting to read that thread in the context of Garner's assertions about normality.There's a thread here on his insight here:
I think this is a big factor in the deeply rooted denial of the realities of ME, et al, by both the medical profession and everybody else.Garner's behaviour explains so much about Cochrane, doesn't it? The anti-pharma and the pro-lifestyle changes bias.
In the end it all seems to come down to difficulty adjusting to the reality of having a mortal, vulnerable body and the existence of terrible uncontrollable diseases.
I can understand if someone needs positive thinking beliefs to manage their fears. There's just a problem when there is also claims that it's an actual treatment.
I got sick in 1984 and did not get diagnosed for over four years. I had never heard of ME before being diagnosed, and I couldn't possibly have heard of CFS because the term didn't exist for the first three years I was sick.Yes, so many people who were ill long before any forum or information on the internet had positive beliefs that they would get better and tried ever so many things.
Even now when people get ill there has been so much positive press for exercise (and has done for decades) that I expect there's barely anyone (Until covid and twitter) that did not have the idea that exercise would be good for getting back to normal.
To be cost effective a therapy has to be clinically effective first.EDIT - just occurred to me that the NICE Committee, which produced the new guideline, dismissed some interventions on the grounds that they didn't represent value for money - so Paul Garner's claims fail the test of being cost effective - even if you accept that they work for some people. I haven't seen any credible evidence that they do work.
I agree and I'm not aware of any objective evidence that these interventions work - if fact the objective evidence indicates that they don't work e.g. the PACE trial participants didn't return to their previous healthy lives --- return school, hours worked* ---To be cost effective a therapy has to be clinically effective first.
The more I see of Garner's antics the more I feel moved to contact him and point out what a complete fool he is making if himself, along with Flottorp.
If I did Twitter I would have tweeted by now. But I am glad I don't.
Also, how does he manage to claim that the Spanish influenza "was probably coronavirus"?
Please, can his colleagues discourage him from talking to the media. He is not helping himself and he is certainly not helping humanity.
(It was alphainfluenzavirus H1N1. It started in the US, not Spain.)
Given how gross a mistake that is for someone so apparently qualified to know better, I begin to wonder if it really was a mistake on his part, or a deliberate attempt to mislead those who would not know better, but would instead blindly accept the word of someone with his qualifications?For a professor of infectious diseases, that's a pretty basic mistake i.e. "Spanish" flue was a coronavirus!Also, how does he manage to claim that the Spanish influenza "was probably coronavirus"?
Please, can his colleagues discourage him from talking to the media. He is not helping himself and he is certainly not helping humanity.
(It was alphainfluenzavirus H1N1. It started in the US, not Spain.)
Yea it seems slightly weird.Given how gross a mistake that is for someone so apparently qualified to know better, I begin to wonder if it really was a mistake on his part, or a deliberate attempt to mislead those who would not know better, but would instead blindly accept the word of someone with his qualifications?
Yea it seems slightly weird.
From memory the virus which caused "Spanish" flue has been characterised/sequenced - it was isolated from frozen bodies in the (North American) Arctic.