wombatwoody wrote on Jul 17^th, 2022 at 3:51pm:


I am suggesting you seek out and quote morons

wombatwoody wrote on Jul 17^th, 2022 at 2:43pm:


It tasted like you are incapable of independent thought.

wombatwoody wrote on Jul 18^th, 2022 at 6:51pm:


Why does this ignorant BS not get bans, but I do for telling the truth?

Sir lastnail wrote on Jul 17^th, 2022 at 1:00pm:


About that pic of the thalidomide babies:



Dr John D. Flack – The Daily Sceptic Feb 7, 2022

I joined Beecham Research Laboratories in 1970 as a pharmacologist/endocrinologist...

The pharmaceutical industry was still reeling from the thalidomide disaster and the industry along with Government regulatory authorities worked together to do as much as was possible to avoid such tragedies ever happening again. It was perhaps quite understandable, then, we were ultra-cautious, and I have no doubt that on the faintest whiff of any safety problem we ‘failed safe’ and almost certainly ‘threw the baby out with the bath water on many occasions. The industry and regulatory authorities were obsessed in putting safety over efficacy. Getting a drug through the preclinical and clinical stages of safety testing was not only very expensive but invariably took more than a decade. Patent law was changed to give an extended period for exclusivity to allow for the industry to have any chance of making a return on investment...

Coupled with this the industry was seen as a very convenient ‘whipping boy’ by the print and TV media. There was hardly a week when BBC Panorama wasn’t exposing some scandal. Making money by trying to make the sick well was seen as a positively evil objective. Investigative journalism was the way to journalistic stardom. What a contrast to the situation we see today. To all intents and purposes over the past two years the Government regulatory authorities, academia, mainstream media and industry appear to be sharing the same bed – all very cosy! Gone, it seems to me, are the checks and balances that we had in the 1980s that provided the public with some sense of confidence that the medicines being marketed were both effective and safe. Academics are frequently charged now with having vested interests. Securing grant money for research is now a matter for international consideration. Witness the huge amount of funding our universities now receive from China and the Gates Foundation. Who can blame the sceptics cry of ‘follow the money’?

So it was that in 1980 I transitioned into pharmaceutical development and became Director of Safety Evaluation of the newly named Beecham Pharmaceuticals. This grand title – again reflecting the emphasis on safety – at ground level meant managing the toxicology and metabolism/pharmacokinetic departments for a decade. Though a raft of safety studies had been agreed to try to guarantee safety, how was it possible to trust the industry to do these studies in strict accordance with the Government regulatory guidelines? Thus, the implementation of formal inspections by the Government regulatory authorities to monitor Good Laboratory Practice (GLP), Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP). No stone would be unturned during these inspections, and I recall now the many sleepless nights mentally wrestling with the inspectorate from the USA Federal Drug Agency and the U.K. Safety of Medicines Department – now called the MHRA (Medicines Health Regulatory Authority). However, it must be said that though there was most certainly, and rightly, an adversarial atmosphere, there was always a recognition that the joint goal was to provide effective medicines that were safe.

With this background, we come to December 2020, when, under emergency measures, ‘vaccines’ still in the experimental phase of development were rolled out with much fanfare to immunise the vulnerable population against the new viral disease of COVID-19. If this was something of a surprise, there was also the knowledge that previous attempts to discover effective and safe vaccines against earlier strains of this type of virus, namely SARS-1 and MERS, had failed. Furthermore, historically, coronaviruses in general had not proven to be amenable to conventional vaccine technology.

Annually the general population are offered ‘flu vaccines – few are concerned about their safety, and rightly. Not too much concern either as to their efficacy, but who cares if they are safe. Surely these new ‘vaccines’ can be considered in a similar manner? No, I am afraid not. These new gene-based ‘vaccines’ are working in a completely novel way – nothing remotely resembling that of traditional vaccines. Given that pharmaceutical companies work competitively it was also somewhat of a surprise they took the same approach of targeting what has been termed the ‘spike protein’ of the SARS-CoV-2 virus. This protein is nasty – sometimes being referred to as a ‘pathogenic protein’ – and is recognised as causing many of the awful pathologies associated with the disease of COVID-19. Logically you would inactivate or at least attenuate this nasty spike protein and develop a vaccine around the attenuated virus. But that’s not what was done. These ‘vaccines’ do not contain any of the offending virus at all but rather the gene sequence that causes the nasty spike protein to be made in the body. We have little idea how much of this nasty protein is produced or for how long it lasts after an injection of the gene sequence...

cont'd next post

wombatwoody wrote on Jul 18^th, 2022 at 10:13pm:


Were you stillborn, wombat?