Excellent video from Neil Oliver - Amnesty is not possible until there is an apology for behaving like "people in uniforms"

Five minute video from the smart and articulate Neil Oliver - who is far too polite in his condemnation of those that wanted to segregate, demonize and vilify those of us who refused to take part in the experimental injections of mRNA THAT FAILED CLINICAL TRIALS.

Neil Oliver asks why we should be expected to sweep Covid hysteria under the rug? - YouTube

https://www.youtube.com/watch?v=RrcLjOaALEg

Remember many politicians and health regulators, globally, but especially in Lithuania, Canada, Australia and New Zealand, wanted to place the unvaxxed into internment camps and deny them all human contact with the outside world inhabited solely by the vaxxed.

All because the vaxxed thought that injecting instructions to create toxins would cure them of the very same toxins that they thought were harmful, whilst at the same time preventing infection, transmission, hospitalization and death.

What Neil did not cover were the harms that instructions within C19 mRNA injections will do for a generation of mankind.

The world is now within a whisker of administering 13 billion of these injections, with 68% having received at least one dose. That means that the 5.4 billion people that have received at least one dose, average 2.4 doses each.

The outcomes of these injections were shown in the Pfizer/BioNTech Phase 3 clinical trials here - a clear fail of the trial.

The COVID-19 Inoculations - More Harm Than Good FINAL Video & Print (canadiancovidcarealliance.org)

https://www.canadiancovidcarealliance.org/wp-content/uploads/2021/12/The-COVID-19-Inoculations-More-Harm-Than-Good-REV-Dec-16-2021.pdf

Here is the damning slide on page 33 of that 51 page slide deck.

The sole end point of the clinical trial was to reduce symptoms of disease. Not to reduce infection or transmission and not to reduce hospitalization or death. Those symptoms of C19 disease are in the rows titled “Related Adverse Event” and “Any Severe Adverse Event” qualified by NOT requiring hospitalization. The higher numbers of +300% and +75% for the injected group v the placebo group speak for themselves.

The Pfizer/BioNTech injections FAILED the clinical trials and were approved by the FDA and CDC - and by equivalent health regulators in almost every other country - despite the FAILURE of the trials for the injections.

Now look at deaths. Although there is less statistical significance in these numbers, there is still excess deaths in the injected group v the placebo group of almost 50%.

And still the FDA/CDC approved the injections.

There were around 21,920 in each of the injected and placebo groups in the trial. Every pandemic has a beginning, a middle and an end. The current Omicron C19 variant has a far lower lethality than the original “wild” strain. If you were to re-run the clinical trial today, there would be far fewer fatalities in the placebo group BUT THE HUMBER OF FATALITIES IN THE INJECTED GROUP WOULD NOT CHANGE.

What you are left with is 20 out of 21,900 all cause mortalities in the injected group of the Phase 3 clinical trial. A lethality rate for those double dosed in the trial of around one in 1,000 (one in 1,095 to be precise). In (a short and unblinded) SIX MONTHS of the clinical trials. There has been no follow up data on outcomes for those injected - it would still be relevant to know how many of those injected died in the six months after the trial, the year after the trial and the (almost) two years of the trial. Where is this information - surely Pfizer has it (and Moderna for its trial).

For those 5.4 billion injected an average of 2.4 times each, the Phase 3 clinical trials indicate that likely around 5 million will have died in the first 6 months after being injected.

Adverse event reporting systems in Europe and the US indicate that this is around 1/4 of those that have died - reflecting the bias in the populations selected in the injected and placebo groups of the Phase 3 clinical trials and a worse real world experience - and also failure to trial the “scale-up” from a few thousand doses to billions of doses requiring proper freezing and thawing of injections that did not go through this vital end point in the manufacturing process.

Once again, even before the injections were rolled out, NO ACCOUNT WAS TAKEN OF THE RECOVERY RATE. Infections last around 15 days - the clinical trials lasted (a short) six months. The recovery rate globally for those (falsely) diagnosed as C19 “cases” using the “not fit for purpose” RT-PCR test is now 621 million “recoveries” out of 641 million “cases” = 97%. Maybe just 823 out of 857 “cases” in the placebo group were actually still infected at the end of the clinical trial.

Had these “recoveries” been factored in to the Phase 3 clinical trial, the much vaunted “Relative Risk Reduction” would have been obviously placed in the context of an “Absolute Risk Reduction” of ZERO to the nearest percent.