I understand people not wanting to promote things like that, but linking to an archive site can be useful for the future. Sympathies to those in Norway...
To be fair to the GMC on this, maybe they recognise that they're not up to the job of deciding what is or is not misinformation?
Doctors promoting anti-vaccine nonsense is bad, but do we think that the GMC is up to the job of deciding what doctors should or should not say? There are things that...
I think that there's a danger that any medical professionals, however well intentioned, will have a negative impact on how 'pacing' is understood if they start to make a career from providing 'pacing'. It seems that medical culture makes it really difficult to make a virtue of leaving patients...
Recovery Norway promoting Vinay Prasad's video on this paper, titled 'Long COVID has nothing to do with COVID in kids! Loneliness and poor physical activity'
https://www.facebook.com/RecoveryNorway/posts/pfbid0dLmwhpgSN5muPqPVnjDnxsXVWpqNivL1vtGVnF3KMi9hi1xmQzY2fZF7cLst9fGRl
This webpage listing Recovery Norway as the organisation for this project is of interest: https://dam-no.translate.goog/prosjekter/langtidseffekter-etter-koronavirusinfeksjon-hos-ungdom/?_x_tr_sl=auto&_x_tr_tl=en&_x_tr_hl=en-US&_x_tr_pto=wapp
Elias Brodwall and Wyller are authors of the JAMA...
According to the linked to document Stephen J. Kirsch, M.D was the doctor who Unum initially turned to to assess this claimant, and he want against the advice of her doctors in claiming she was able to return to work. Scott Norris, M.D was the Unum doctor who denied her appeal.
I think it can...
Not read the paper yet, but interested in all the discussion.
One thing I thought to add is that while I share people's tendency to be most interested in discussing the things I'm more critical of, it can also be good to acknowledge the work that's gone into papers that seem to be making a...
BBC journalist Lucy Adams talks about her experiences with Long Covid, and Alan Carson: https://www.bbc.co.uk/news/uk-scotland-65058119
She said: "He was the first person who could explain in a way that I understood what was happening to me and how the communication systems between my brain and...
Interesting discussion on Vogt's FB page about this:
https://www.facebook.com/HenrikVogtMDPhD/posts/pfbid02q2QVhWgi3RhopXV3W1BbHe3wo3MaohVD1KH36fTbn66GpQvcUMmLmFiBo9RxLj8rl
Also, funny the Vogt introduces his comment with "Below you can read clarifications from Recovery Norway of some...
I agree with others that 'believing patients' isn't the best way of thinking of this (did the patients even start making claims about sonic weapons? I thought that was others), and if you start rejecting views just because other people hold them, that's only going to make it easier for them to...
The various 'sonic weapons' theories floating about always seemed pretty questionable imo. When the CIA is promoting it it's difficult to judge - maybe they'd cooked up some bizarre secret weapon themselves - but there was never much in the way of evidence to support that view.
When the whole...
But even there, where even the supportive journalist seems wary of Garner's vociferousness, it's not made clear who 'the activists' or 'these people' are exactly, and what marks them as 'us'. The whole article seems so lacking in specifics that it's difficult to draw much of substance from it...
What quote from Garner do you think is the most clearly despicable example of him using this e-mail (or others) as a weapon against 'the ME community' or trying to silence legitimate criticism?
I've not re-read the article, but my impression is that there's a move towards more cautious and...
I think that it also depends on specifics, and that many of those specifics are more favourable to Garner than the SMC.
I think it's fair for patients to provide accurate quotes from researchers and doctors that illustrate troubling behaviour, and if Garner is getting e-mails like the one...
I think that the specifics of the promotion of 'positive thinking' to ME/CFS patients has been one of the most destructive things to surround the condition, and an important part of why things are so bad now. But I also think that there is doubt here, and maybe I'm wrong. Some ME/CFS patients...
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.