Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

Oh i bet they will give it to him... after all he has faced such hostility for simply sharing his story of recovery. But he kept telling his truth in the face of militant activists. He will get it for sure, or at the very least an 'honourable mention'.
 
Who has been rattling his cage?

"NICE guidance on ME/CFS is the most extraordinary corruption of the evidence-based guidelines process I have ever seen. See this article in the Lancet"
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https://twitter.com/PaulGarnerWoof/status/1579099446448885760
 
total recovery in less than 4 weeks. says no LP(?)

Interesting that Paul Garner has now edited out of his story ‘that phone call to Norway’ that is understood to have been to an LP practitioner.

It is worth noting that his personal testimony of positive thinking as a cure for Long Covid has developed over time, for example his initial public appeal for help from the ME community is subsequently edited out of his latter attack on us as a source of uninvited harassment, rather weakens it as a source of objective un ‘cherry picked’ evidence.
 


Tweet from Sense about Science: “We were delighted to meet and hear from Paul Garner last week, who discussed his recovery from long Covid and the importance for scientists to be able to share their research without any fear or intimidation. @CochraneUK #MaddoxPrize


Who has been rattling his cage?

"NICE guidance on ME/CFS is the most extraordinary corruption of the evidence-based guidelines process I have ever seen. See this article in the Lancet"
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https://twitter.com/PaulGarnerWoof/status/1579099446448885760
Call me cynical, but we've seen this sort of behaviour before from M Sharpe who did his best on Twitter to provoke 'attacks' so they could be used by a journalist in an article claiming he'd suffered harassment.

I don't think Garner's tweets today are just an innocent coincidence with him meeting the organisation that has awarded the Maddox prize to Wessely in the past.
 
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