Discussion about this post

User's avatar
Michael McCabe's avatar

Thank you for an excellent piece. It is good to see a public health expert looking at an issue from from multiple points of view.

Failure to consider other points of view and maintaining the "do not question what we say" orthodoxy during the pandemic eroded faith in public health experts. It will be decades before that faith recovers. Pieces like yours are a step in the right direction.

I particularly liked the Franklin quote. We would all be well advised to consider his sage advice.

Expand full comment
Baya Lazz's avatar

"Compelling as these data are"

They are not compelling at all. There is as much evidence to support the idea that having a world war resulted in health improvements i.e. none, just a correlation. The evidence for homeopathy is more compelling since it accounts for the placebo effect where as 'vaccine' 'science' is pseudoscience that avoids valid controls or admitting the effects of placebo and nocebo making it doubly misleading.

https://www.elsevier.es/en-revista-clinics-22-articulo-homeopathy-is-not-placebo-effect-S1807593224001339

"three main end points being discussed in the literature on COVID-19 vaccine efficacy: symptomatic COVID-19 and serious or critical COVID-19 disease. "

These are surrogate endpoints that simply involve getting a 'pcr test' to respond. This is not evidence of any reduction in symptoms or health improvements and could even represent an adverse reaction. No clinical endpoint is even being investigated but the reader is lead to assume reducing a test result would be beneficial. A test that has no fixed definition and has already been changed to different primers a number of times.

"The use of surrogate endpoints is [...] not unproblematic. In the past, there have been

many situations in which relying on surrogate endpoints was misleading or had fatal

consequences

despite strong correlation with the clinical endpoint. This problem has been known for

more than 30 years. [...] Some products that were approved on the basis of surrogate

endpoints had to be withdrawn from the market at a later date because the benefit-risk

balance was reversed in studies with mortality or morbidity endpoints.”

Source: DIMDI, Cologne 2009

https://truthseeker.se/wp-content/uploads/Stefan-Lanka-The-Misinterpretation-of-the-Antibodies-English-Translation.pdf

Expand full comment
1 more comment...

No posts