The Coagulation Of Evil

"Don't you love farce? My fault, I fear I thought that you'd want what I want Sorry, my dear. But where are the clowns? There ought to be clowns Quick, send in the clowns."

Should there be any doubt whatsoever? … not after this.

It is clear from the statements made by HHS Secretary Bobby Kennedy, Jr. that then POTUS45 (& now 47) DJT’s euphoric ‘Warp Speed’ was both a pantomime and a charade, orchestrated by the United States own National Security Agency ~ NSA (and most definitely not the public health HHS or CDC), although beyond obviously, they colluded.

The second orchestrating agency was The Pentagon.

Was ‘informed consent’ strategically erased? Yes, of course.

The negative-risk benefit, so called “vaccines,” were developed not by Moderna and Pfizer, but by National Institutes of Health ~ NIH (who owned 50% of the patents). The injections were manufactured by military contractors. (Bobby, these entities and persons will eventually require naming).

Pfizer and Moderna were paid to put their corporate stamps on the product. But to be clear as current HHS Secretary Bobby states, it was a military project from the beginning.

---

Below short clips for an exhausted, attention deficit populace. They are short and they are eminently important. Do watch and listen.

"This was a military project from the beginning." Signed, current HHS Secretary Bobby Kennedy, Jr.

Now, with this in mind, when reviewing one seminal meeting publication of the time (March 2020) it might well appear unquestionable that the public face of BigPharma together with the corporate face of ‘vaccine’ developer, the Coalition of Epidemic Preparedness Innovations (CEPI ~ with its absurd conflict of interest vested in funding the Brighton Collaboration, the “safety platform”) was a virtue signalling charade, a veritable parade of evil clowns?

Readers here may be aware of the identities in play, the corporate investment and alignments, and the contributing involvement of national governments to what appears as an evil charade (including New Zealand, Australia, UK, Canada, Germany and all the rest).

As linked above, CEPI appears as the alleged ‘vaccine developer’ while ‘BC’ is the alleged safety platform, the Brighton Collaboration (aka. SPEAC “safety platform”).

It cannot be spelled out more clearly that this entity, a fusion of corporate, bureaucratic and government actors formed a coercive conglomerate that was wittingly and unwittingly tasked with implementing rank evil. It is not possible to form any other conclusion with the established and declared background that they were acting as monstrously overpaid surrogates for the actions of a military and intelligence DeepState.

Let’s Drill Down

Once again, I find myself drawing attention to the following salient and telling remarks made in this published meeting paper:

P.-H. Lambert, D. M. Ambrosino, S. R. Andersen et al., Consensus summary report for CEPI/BC March 12–13, 2020 meeting: Assessment of risk of disease enhancement with COVID-19 vaccines, Vaccine.

The SARS-CoV-2 S protein structure was solved shortly after its emergence and shows similar structure and mobility as the SARS-CoV-1 S. The timing from first knowledge of SARS-CoV-2 to the beginning of the Phase 1 study was a remarkable sixty-five days.

The Fan Wu paper ~ Fan Wu et al. A new coronavirus associated with human respiratory disease in China. In: Nature 580.7803 (2020) simply does not withstand scrutiny and is readily falsified.

It is absurd on its face as is the illusion of ‘a remarkable 65 days’. To wit,

Thus, we were able to substantiate our hypothesis that the claimed viral genome sequences are misinterpretations in the sense that they have been or are being constructed unnoticed from non-viral nucleic acid fragments. In particular, our results underscore the urgent need to perform appropriate control experiments. For each suspected pathogenic viral genome sequence, an obvious protocol would be to attempt assembly of the genome sequences from corresponding non-suspect samples using identical protocols. Structural analysis of sequence data in virology. An elementary approach using SARS-CoV-2 as an example

---

We now have come to understand that there was no pandemic (Rancourt et al. 2023), merely a pandemic of fraudulent testing, here, here, here, here.

But our March 2020 gathering of experts suggested with unbridled enthusiasm that:

The advantages of mRNA vaccines include ability to create a highly precise type of protein to elicit the correct antibodies, to elicit T cell responses that are Th1 predominant, and the rapidity of manufacturing.

Notwithstanding this grandiose assertion, albeit as revealing as it may be, the truth is far more compelling to read when later work in 2021 describing the, Evolution of Anti-SARS-CoV-2 IgG Antibody and IgG Avidity Post Pfizer and Moderna mRNA Vaccinations; Bliden KP et al. (2021) that observed instead (in a concluding comment):

“We did observe highly variable immune responses including those with well below average anti-RBD (‘rigid binding domain’) IgG levels and avidity.”

So, the preposterous assertion of ‘highly precise type of protein to elicit the correct antibodies’ is falsified … as amplified hubris or overblown virtue signalling? You decide.

Meanwhile, the March 2020 meeting of experts advising CEPI/BC revealed a naked truth, namely that the ‘experts’ (see the line -up of authors) disgenuously suggested that they had little to no idea what they were getting into, while displaying the appearance of a high degree of uncertainty illustrated by their ‘consensus comments’ outlined in the meeting publication, where it is summarily stated:

Of course, disadvantages include the novel nature of both mRNA and DNA vaccines without any licensed vaccine with either technology to date and lack of experience for mass production. Therefore, multiple platforms for SARS-CoV-2 are under development that mitigate against some of the potential disadvantages of nucleic acid vaccines.

This is known in the business as manufactured, ‘plausible deniability’.

Post Script

The Impossible Time Line

The meeting of ‘experts’ took place on the 12 - 13 March, 2020.

Their proceedings were published 21 May 2020.

By July 27, 2020, Pfizer has commenced its Phase 2/3 study as stated in the Dec 2020 NEJM publication, Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine; Polack FP et al.

In an ongoing multinational, placebo-controlled, observer-blinded, pivotal efficacy trial, we randomly assigned persons 16 years of age or older in a 1:1 ratio to receive two doses, 21 days apart, of either placebo or the BNT162b2 vaccine candidate (30 μg per dose). BNT162b2 is a lipid nanoparticle–formulated, nucleoside-modified RNA vaccine that encodes a prefusion stabilized, membrane-anchored SARS-CoV-2 full-length spike protein.

Between July 27, 2020, and November 14, 2020, a total of 44,820 persons were screened, and 43,548 persons 16 years of age or older underwent randomization at 152 sites worldwide (United States, 130 sites; Argentina, 1; Brazil, 2; South Africa, 4; Germany, 6; and Turkey, 9) in the phase 2/3 portion of the trial. A total of 43,448 participants received injections: 21,720 received BNT162b2 and 21,728 received placebo (Figure 1). At the data cut-off date of October 9, a total of 37,706 participants had a median of at least 2 months of safety data available after the second dose and contributed to the main safety data set.

Hon. Grant Robertson, New Zealand Minister of Finance, signed-off Pfizer liability waivers apparently notifying the NZ parliament of the Pfizer and BioNTech indemnity on 22 November, after granting it, astonishingly, to Pfizer on … 5 October … as reported, BEFORE the study data cut-off date of October 9 (!)

…when a total of 37,706 participants had a median of at least 2 months of safety data available after the second dose and contributed to the main safety data set. (since then we know the Pfizer study data is as useless and rancid as old Swiss cheese) while the former New Zealand Finance Minister has been elevated to status as Vice Chancellor of Otago University on annual salary of NZ$629,000.

Meanwhile, NHS England trumpeted the dawning of a new age:

8 December 2020

The biggest vaccine campaign in NHS history kicked off this morning, as 90-year-old grandmother Margaret Keenan became the first person in the world to receive the Pfizer COVID-19 jab following its clinical approval.

It therefore took slightly over an utterly impossible 6 months from the CEPI/BC Lambert et al. (2020) publication of doubt and uncertainty to the industrial scale implementation of modRNA/LNP shots.

Conclusion

It stretches the bounds of credulity when reviewing the meeting comments of the experts advising CEPI/BC that from the date of its publication (21 May 2020) and given a declared … “novel nature of both mRNA and DNA vaccines without any licensed vaccine with either technology to date and lack of experience for mass production” … that in 2 months by, July 27, 2020, 21,720 participants were slipping into place to receive injections with BNT162b2 injections that were on the cusp of mass production in sufficient quantities to be globally distributed, all participants/’controls’ recruited, countries signing off on contracts, and engaged to undertake the ‘Phase 2/3 part of a global phase 1/2/3 trial evaluating the safety, immunogenicity, and efficacy of 30 μg of BNT162b2 in preventing Covid-19 in persons 16 years of age or older’ with an alleged data cut-off of October 9… and by …

Dec 8, 2020, NHS England medical jabsters were hard at it with the rest of the planet hard on its heels.

Ehh, no. Absolutely not.

As Bobby inferred at the beginning of this commentary, everything was good to go in 2020. The very mortal, self-appointed gods decided to push their demonic button in 2019.

I leave you with a final and obvious thought, and if you will, a proverbial ‘call to arms’.

Fool me once shame on you. Fool me twice, shame on me.