Formal scientific institutions took a battering during the pandemic, and deservedly so. From the wildly inaccurate predictions of SAGE modellers to the denial of natural immunity by signatories of the John Snow Memorandum, ‘Science’ (uppercase ‘s’) has not had a good three years.
A particularly striking illustration of this is citation patterns in the scientific literature. If things were working well, the best studies would get cited the most. Unfortunately, that appears not to be the case: citations have flowed disproportionately to studies that uphold The Narrative.
In June, 2020, researchers from Imperial College London (including our old friend Neil Ferguson) published a paper in the prestigious journal Nature titled ‘Estimating the effects of non-pharmaceutical interventions on COVID-19 in Europe’.
They concluded – on the basis of a complex model-fitting exercise – that lockdowns had saved the lives of 3.1 million people across 11 European countries. That’s right, 3.1 million lives saved, and during the first three months of the pandemic alone.
Doesn’t sound very plausible, does it? After all, Sweden didn’t lock down, and they saw about as many deaths – or even fewer – than the countries that did lockdown. So how did the researchers get to the figure of 3.1 million lives saved?
As Philippe Lemoine notes, they just assumed that death numbers would have been far greater in the absence of lockdowns, and then took the difference between those numbers and the ones that were actually observed, and concluded the difference was due to lockdowns. Okay, but what about Sweden?
Well, the researchers fit a model in which the effect of different interventions could vary from country to country. And while Sweden didn’t have a lockdown, they did have a ban on public gatherings (of more than 500 people). So in the researchers’ model, Sweden’s ban on public gatherings ended up having the same impact as lockdown in all the other countries.
They were effectively claiming that, in France, Italy, the UK etc., lockdowns succeeded in preventing hundreds of thousands of deaths, but in Sweden, the same effect was achieved by simply banning public gatherings. Like I said, not very plausible. In fact, it’s preposterous.
The paper has beenheavilycriticised. However, that hasn’t stopped it being cited 2779 times! Most researchers don’t get that many citations in their entire career, let alone on a single paper.
Now let’s look at the number of citations accrued by papers finding that lockdowns didn’t have much effect.
Simon Wood’s paper ‘Did COVID-19 infections decline before UK lockdown?’ concluded that “infections were in decline before full UK lockdown”. It has been cited a total of 40 times (across two different versions).
Christian Bjørnskov’s paper ‘Did Lockdown Work? An Economist’s Cross-Country Comparison’ found “no clear association between lockdown policies and mortality development”. It has been cited a total of 57 times.
Eran Bendavid and colleagues’ paper ‘Assessing mandatory stay-at-home and business closure effects on the spread of COVID-19’ did “not find significant benefits on case growth of more restrictive NPIs”. It has been cited a total of 205 times.
Christopher Berry and colleagues’ paper ‘Evaluating the effects of shelter-in-place policies during the COVID-19 pandemic’ did “not find detectable effects of these policies on disease spread or deaths”. It has been cited a total of 68 times.
While none of these papers is perfect, they’re all vastly more rigorous than the Imperial College study published in Nature. Despite this, none of them has garnered even 1/10th as many citations as that study.
Something has gone seriously wrong when a flawed study gets almost three thousand citations, while more rigorous studies only pick up a few dozen. As to what explains this disparity, I can only speculate that most scientists haven’t come to terms with the fact that the ‘experts’ dropped the ball.
Right from the outset of the ‘plandemic’ there have been those who recognised the evil in what was going on and who, in their own ways, have been making every effort to resist. Across the world many people have lost their jobs and their businesses, but perhaps giving up one’s livelihood on principle is the supreme act that a person with moral courage can do to oppose the enemy that confronts us.
There have been many such brave souls and Mark (not his real name) is such a person. A teacher at a large secondary school in Yorkshire, he realised that he would have difficulty doing his job when testing and then masking of his pupils was mandated. These instructions came from the local authority and were expected to be introduced without question. There were other teachers, too, who had grave misgivings, but they were in the minority and were openly mocked.
All teachers were given instructions about the distribution of testing kits and to organise pupil seating plans which had to be adhered to. All staff were expected to wear a face covering; there was no consultation about this. In the spring term of 2021 a box of testing kits arrived in Mark’s classroom, which he left untouched as the holiday was just about to start. On return from holiday he decided to write to the head teacher about his concerns, and you can read his email here.
Not only did the head not reply to this letter, but he didn’t speak to Mark again. Instead, he sent a teaching assistant, who was full on-narrative and was wearing two masks plus a visor, to admonish him for not complying. In Mark’s own words:
‘She commenced by bellowing instructions to maskless pupils to cover their faces. She glanced at me, clearly expecting a reaction. How could I possibly allow these potential vectors of death to be in school without covering their faces? I had never, and still have never instructed a child to obstruct their airways. It is a line I simply cannot cross. I suspect my response was neither wanted nor expected, since it appeared to make her address the children with yet more venom. I turned and smiled at the children instead who smiled back me. These confused souls seemed to prefer my smile to this clown’s anger, despite not being able to see her face.
‘I’m not seeking praise or recognition or anything at all here, I simply cannot in good conscience do it. As the school year progressed, things didn’t improve. Every few weeks she would arrive to carry out the task, a task that she clearly felt I should be doing and one I had no grounds to refuse. After she left the room, the masks would come down and an ever-increasing number of testing kits were discarded by the kids into the bin each time. My attitude was clearly causing an issue for some members of staff; many would blank me as we crossed in the corridor, and entering the staffroom sometimes felt like the scene from the movie An American Werewolf in London when the tourists walk into the Slaughtered Lamb pub and everyone suddenly stops talking to stare.’
When you read these words, describing the experience of a dedicated teacher who was untouched by the brainwashing that resulted in utter cruelty being inflicted on children across the country, it makes you shudder in disbelief. For Mark to maintain his moral stance in the face of such disgraceful behaviour from his colleagues surely speaks volumes for his strength of character. How on earth he managed to carry on, day after day, in the face of such hostility is a credit to his courage and steadfastness, not to mention his dedication to his pupils.
In July the headmaster was off work because he had tested positive for Covid. In his absence his deputies, clearly relishing the authority, upped the ante from passive-aggression to a decidedly more unpleasant tack. Mark’s pupil-centred teaching technique was deemed unsafe because he was not wearing a mask, did not sport PPE and was doing his best to help the kids in his charge by behaving in a ‘normal’ manner. He was told to go home, take a test or, if he preferred not to get tested, then allow other teachers to cover his classes for two weeks.
Confronted with such stupidity and total lack of any humanity regarding the care of pupils, Mark was pushed over the edge when another masked deputy began haranguing him about following ‘the science’. An argument ensued. It was the final straw and he collected his belongings and left for good.
Mark gave up a career that he enjoyed tremendously because he would not subject his pupils to the Covid madness. The welfare of the children in his charge was always at the centre of his actions and he could not, in all conscience, inflict the insanity of masks, tests and distancing on his young charges.
As a conclusion, it is heartening to say that Mark now works as a supply teacher and devotes much time to opposing the narrative with practical actions. The wonderful thing from his point of view is that he stood by his conscience and has the satisfaction of going forward knowing that he kept his soul intact. One wonders how his headmaster, his deputies and other teachers who inflicted these despicable practices on young, impressionable youngsters justify their behaviour now that the truth about the Covid crimes is breaking by the day. Did they keep their souls intact? I think not.
It is well known that homeless populations have much higher rates of hospitalization for a variety of reasons including drug abuse, alcoholism, aspiration, pneumonia, and neuropsychiatric reasons. I have always wondered how they fared during COVID-19 having heard little about severe outcomes among those who live outside.
Lucie Richard and coworkers reported on 736 homeless individuals in Toronto, Ontario during 2021 and 2022. The majority managed through the illness with no reported difficulty over the time period, most with the Omicron variants. There were no reported severe cases, hospitalizations, or deaths.
Despite approximately two thirds taking a COVID-19 vaccine, the shots appeared to be useless in this population with no statistically significant vaccine efficacy. While the public has watched the relentless pursuit of well-employed adults, college age students, and children down to 6 months of age, the most economically deprived and vulnerable in society appear to be of little interest to the Biopharmaceutical Complex, and like the other groups, have no theoretical benefit from vaccination. As a general rule if the highest risk derive no reduction in hospitalization or death, then even lower risk individuals are not worth the effort for public health interventions such as vaccines.
The Medicare data proves that the flu vaccine is too unsafe to use because it kills more than 1 person per million vaccinated, which is the safety threshold noted by vaccine expert Paul Offit.
The evidence has been in plain sight but nobody seems to care.
Introduction
I find it really annoying that our government is hiding the safety data on vaccines. How does hiding the data protect the public from harm?
Of course, I’m not a doctor and doctors don’t have any problem at all with their government hiding safety data. Have you ever seen any of them complain about the lack of transparency? Of course not! None of them want their licenses revoked or their grants canceled.
However, since I’m not a doctor, I’m not encumbered.
So I wanted to let you in on a little secret: the government hides the data from us because the vaccines they’ve been promoting are unsafe.
Let’s take the flu vaccine for example.
Have you noticed that the government NEVER shows you the data from Medicare, VSD, BEST, or any other database?
The reason is simple: the shots are deadly and should be pulled. If they released the data, everyone would know this. So they keep the data hidden from public view.
Thanks to an anonymous HHS employee, I’ve been provided with the “days after death” for the flu vaccine.
I’ve already published the flu charts twice before (here and here) and nobody noticed, even though I pointed it out in my Feb 25 Game Over article, so I’m going to point it out once again now.
Figure 1. Number of deaths per day after taking the flu shot. See the spike on Day 0? It’s easy to miss if you aren’t looking. That’s a problem. That could only be caused by the vaccine itself. There is no other way to explain this “coincidence.”
See the spike on Day 0?
At least 375 “excess deaths” on Day 0!
Last I checked, there is no need to vaccinate people for the flu right before they die because the vaccine takes time to have an effect. That’s why there is normally a reduced number of deaths on Day 0 vs. baseline: if you are about to die, they aren’t going to waste time vaccinating you.
But you can see there are 375 excess deaths on Day 0.
Now consider that this is a subset of all the people who get the flu vaccine in 2021:
It’s only people in Medicare
It’s only people who got the flu shot in Q1 of 2021
It’s only people < 80
375 excess deaths times 1M is more than the population of the US.
So over 1 person per million died.
Summary
The flu vaccine kills > 1 person per million vaccinated.
This means the flu vaccine should be pulled from the market.
I don’t know how I can make it any clearer than that.
And the COVID vaccine? Well, it’s killing people at a 1,000X greater rate than the flu shot. It should have been pulled long ago. Check out this analysis by Denis Rancourt that, after accumulating 100K views, was pulled from ResearchGate. It’s a quality analysis. For example, one of my colleagues who NEVER texts me on ANY papers, texted me to look at this one: “Just published. This data is really stunning.”
But the health authorities are looking the other way and the doctors just blindly do whatever the CDC says, no matter how many people are killed.
The contamination of mRNA vaccines with DNA is far greater than initially thought at up to 35%, and the DNA’s role in inducing human cells to produce the spike protein long term has been confirmed, according to the latest research.
Earlier this month, the Daily Scepticreported on the work of Dr. Kevin McKernan and his team who had subjected the mRNA vaccines from Pfizer and Moderna to deep sequencing analysis and found alarming levels of DNA contaminants known as plasmids. These are small circular DNA molecules that in principle can self-replicate in bacterial and human cells and induce the cell to produce the SARS-CoV-2 spike protein long term. Each vaccine dose was found to contain billions of these plasmids.
The Moderna vaccine appeared to contain DNA contamination at around the ‘safe’ level set by the European Medicines Agency (EMA) at the equivalent of one part per 3,000 mRNA molecules, though it’s not clear how safe this level really is. The Pfizer vaccine, on the other hand, was found to contain DNA contamination at 10 times the ‘safe’ level, at one plasmid per 350 mRNA molecules.
The DNA is part of the vaccine manufacturing process, providing the blueprint for the mRNA, but it should have been removed to at least the ‘safe’ level, though was not for reasons that are unclear.
Now, Dr. McKernan and his team have undertaken further analysis and found that the level of DNA contamination is much greater than originally reported, with up to 35% of the vaccine product being this DNA contamination. They write:
This equates to 20-35% of the nucleic acid in each vaccine being expression vector. This is several orders of magnitude over the the EMAs limit of 330ng/mg. With these levels of contamination, RT activity from LINE-1 is not a prerequisite for genome integration.
Molecular biologist Dr. Jessica Rose explains that this means each dose may contain trillions of DNA molecules, 100 times greater than previously reported: “The left-over expression vectors used to manufacture the mRNAs are at contamination levels 100-fold higher than originally proposed and imply trillions of DNA molecules per dose. This has implications for integration into our genome.”
The precise level of contamination is unknown as these are estimates with a wide margin of error. It may also vary by batch. What is certain, however, is that the contamination of both Pfizer and Moderna vaccines is way above any official ‘safe’ level.
In the original analysis, Dr. McKernan had been looking primarily for RNA contamination and had used an additive that can suppress DNA amplification. By looking specifically for DNA contamination he and his team found that the amount of DNA present was far greater than the initial technique had indicated.
Further analysis by Dr. McKernan and his team has also confirmed that the plasmids are intact and capable of self-replicating, and that the relevant promoters are present that allow them to express mRNA for spike protein in human cells (and not just in bacteria).
This indicates that these DNA plasmids are likely to survive for long periods, be taken up by cells inside the body and induce the cells to produce spike protein for an indefinite period of time.
It is thought this could explain the observed persistence of spike protein in the blood of vaccinated persons for weeks or months after injection, which is believed by experts to be a contributor to adverse effects of the COVID-19 vaccines.
Dr. Jessica Rose notes: “It is more than likely that these adverse effects are the direct result of t he contamination illuminated by Kevin and his team.”
These findings are obviously highly disturbing. Regulators ought to be making a priority of looking into these issues for themselves and, if confirmed, taking the appropriate action including removing the products from the market.
Way back in the spring of 2020, the provocative title of an article caught my eye. Upon reading it, I learned that researchers were rushing to create a vaccine before the COVID-19 virus mutated, which would render the vaccine nugatory and destroy all hopes of creating a blockbuster panacea. Curious at the time, such a warning can be viewed today as having been prophetic. (Note: That article, which offered a business slant on the historic vaccine competition, is no longer available through Google—“some results have been removed,” and are seemingly irretrievable—but here’s one with a similar title from April 2020: “Coronavirus mutation could threaten the race to develop vaccine.”)
“Viruses that replicate in the human respiratory mucosa without infecting systemically, including influenza A, SARS-CoV-2, endemic coronaviruses, RSV, and many other “common cold” viruses, cause significant mortality and morbidity and are important public health concerns. Because these viruses generally do not elicit complete and durable protective immunity by themselves, they have not to date been effectively controlled by licensed or experimental vaccines.”
Accustomed as everyone is by now to a relentless barrage of contradictory proclamations and retaliatory responses to them, the claim that mRNA was never fit to purpose for rapidly mutating coronaviruses might be written off by the usual suspects as the ravings of yet another antivaxxer conspiracy theorist. Except that this paper was co-authored by Dr. Anthony Fauci, the most visible and persistent pusher of the newfangled COVID-19 vaccines throughout 2021 and 2022. So what happened?
Against all conventional wisdom on the ethical practice of medicine, Fauci did everything in his power to achieve maximal uptake of an experimental treatment by human beings across all cohorts, without regard to patient health, age, or any other identifying factor beyond their possession of an arm into which to inject a novel product granted Emergency Use Authorization (EUA) after an accelerated review by the Food & Drug Administration (FDA). Not only did Fauci ignore the vast disparities in vulnerability to severe illness and death between healthy infants and frail nonagenarians, but he also conducted himself for two years as though natural immunity through previous infection were somehow irrelevant to the question of whether a patient should roll up his sleeve.
Now, in the light of Fauci’s own published scientific findings, it would appear that he was right, in a sense, about natural immunity all along, albeit in an unexpectedly perverse way. First of all, as we already witnessed in real time, coronaviruses as a class, including SARS-CoV-2 (COVID-19), mutate rapidly in order to propagate themselves. This “discovery” served as the basis for the development of “boosters,” which, it was claimed, became necessary when “fully vaccinated” persons continued to become infected with COVID-19. Major outbreak-inducing strains such as Delta and Omicron, which arise through mutation, will always be one step ahead of last year’s vaccines, having survived precisely by evading the antibodies induced by injection into the body of the previous virus generation’s mRNA.
According to Fauci’s own findings, however, there is a second, even more compelling reason for denying that either vaccine or natural immunity to COVID-19 can ever be permanent. The primary difference between diseases such as measles, for which vaccines work, and the seasonal flu or SARS-CoV-2, for which they do not, is that the body’s natural immune response rises only to the level of the severity of the pathogen. Since most people can survive coronaviruses, the minimal response needed to defeat the invader is rather mild, which is why immunity dissipates rapidly over time and people can become reinfected again and again, even if they have recovered from natural infection, and whether or not they have undergone vaccination.
There are of course people who die of the flu or COVID-19, but they nearly always have comorbidities, infirmities or weaknesses, rendering them vulnerable to a pathogen which healthy bodies are capable of defeating. Notwithstanding the massive propaganda campaign for universal vaccination, most healthy young persons would have survived COVID-19, and would not have been hospitalized, with or without vaccination. Given the abundance of statistical evidence, there is simply no sense in which it can be truthfully asserted that healthy young persons with no comorbidities were “saved” by the shots. On the other hand, extremely frail and elderly persons can indeed be killed by the virus, regardless of how many “vaccines” they have taken. When it comes to the mercurial class of coronaviruses—instantiated by not only the common cold and the seasonal flu, but also COVID-19—so-called vaccines will never transcend their pedestrian identity as mere shots, for they are constitutionally incapable of offering longterm protection, not only because these viruses rapidly mutate, but also, and more fundamentally, because the body’s natural response to infection by such transitory viruses is never robust enough to be permanent. Just as having survived the flu one year has nearly no bearing on whether one will contract another case of the flu, from a different variant, in the future, no so-called vaccine solution to COVID-19 can confer longlasting protection.
Take as many boosters as you like, until the end of time, but having done so may or may not prevent you from contracting the latest iteration of the virus—or protect anyone else—since every booster or flu shot is the result of researchers’ “best guess” of what the specific properties of the next generation of viruses will be. It appears, then, that the widely celebrated and aggressively marketed, and in some cases mandated, COVID-19 vaccines, paid for thrice by the recipients of “free” shots, were in fact launched on a wing and a prayer. There was really no hope all along that the shots would or could offer longterm protection, although it was claimed for marketing purposes that they were highly effective and would save millions of lives. That those selling points were in fact lies may explain why they were supplemented all along the way with such eerily self-contradictory slogans as: “The vaccinated need to be protected from the unvaccinated!”
Dr. Fauci’s surprising publication reveals that the abundant optimism exuded by him and others in attempting to maximize vaccine uptake was scientifically unfounded from the beginning. Neither the mRNA technology nor the traditional vaccines (which introduce a small amount of the live or dead pathogen into the body to elicit an immune response) can be effective for rapidly evolving pathogens such as coronaviruses to which the highly efficient human body mounts the weakest possible effective response. But this is hardly news, for we already knew long before 2020 that, despite assiduous efforts spanning decades, no one ever managed to develop a vaccine against the common cold. Likewise, the widely touted flu shots, marketed in very public ad campaigns only slightly less aggressive than those for the COVID-19 treatments, are in fact mediocre at best, as Fauci himself has averred.
If vaccine technology, whether vector- or mRNA-based, is simply a mismatch for the nature of rapidly mutating viruses, and this is a matter of common knowledge, readily accessible to anyone working in virology, then how are we to understand Fauci’s comportment throughout the Coronapocalypse? And why did he and his coauthors boldly reaffirm in January 2023 what many other researchers have been saying for years, including a few brave souls who were silenced when they tried to suggest the same from 2020 to 2022?
Fauci faces something of a “Charybdis or Scylla” dilemma here, for if he was ignorant of basic truths of immunology known by competent and knowledgeable scientists before 2020, then he had no business serving as the nation’s fount of public health wisdom. Double-masked Fauci devotees, in the aftermath of what was empirically indistinguishable from a full-scale psyop spanning more than two years, will no doubt remain reluctant to renounce their allegiance to the person who, they believe, “guided” us through the pandemic. Confronted with the revelations of Fauci et al.’s January 2023 publication, such followers may most charitably conclude that the object of their reverence did genuinely believe in the mRNA vaccines and continues to follow “The Science” where it leads, in this case, to finally acknowledge failure.
That Fauci honestly did not know that the mRNA shots would never work has also been the conclusion of a few of his most vociferous critics, including Alex Berenson, who somewhat ironically was spurned as “The Pandemic’s Wrongest Man” by The Atlantic back in April 2021. (Morally speaking, that title surely belongs to Dr. Anthony Fauci himself, for the sheer brazenness with which he defied all known principles of medical ethics in pushing for universal vaccination across all cohorts.) Berenson was banned from social media under pressure by no less a power than the U.S. government itself when he dared to question the Fauci script at the height of the Coronapocalyptic hysteria. (Berenson’s lawsuit alleging the government’s violation of his First Amendment right to free speech is pending.)
Notwithstanding the superficial appeal (and attendant Schadenfreude) of the “Fauci was ignorant and is now eating crow” hypothesis, the Scylla horn of the interpretive dilemma would seem to cohere far better with the character of a man who remarkably responded to his critics on national television that “You’re really attacking not only Dr. Anthony Fauci, you’re attacking science.” Certainly such a person is not someone whom we would ordinarily regard as endowed with the humility needed to admit either ignorance or error. To my mind (and others, such as Dr. Robert Malone, agree) Fauci’s recent publication is yet another gambit perfectly consistent with his comportment throughout the pandemic. While Fauci’s admission that the mRNA technology is not fit to purpose for coronaviruses may on its face seem surprising, in fact, it is entirely true to form.
Yes, Fauci’s gambit is most plausibly interpreted as the latest chapter in his time-tested “fail forward” playbook: to use the outcome of the COVID-19 shot experiment to rally for yet more funding for the pharmaceutical industry. Like all good bureaucrats, Fauci uses government fiascos as a springboard to increase the reach and budget of his domain. In other words, Fauci, having quite effectively painted the COVID-19 virus as the most evil bogey man of them all, is simply continuing his efforts to impel politicians to dole out even more billions of dollars to the government-boosted industry which he has loyally supported throughout his entire career, as has been ably documented by Robert F. Kennedy, Jr. In addition to being consistent with Fauci’s dismissive, smug, and seemingly shameless character, this interpretation coheres well with the general modus operandi of the pharmaceutical industry, which has displayed in recent decades an uncanny capacity to “fail forward” by pivoting and innovating so as to be able to reap massive profits even when their products generate consequences worse than the conditions which they were intended to address.
Note that slippery snake-oil salesmen such as Pfizer’s CEO, Albert Bourla, carefully calibrated their pitches from the beginning so as to protect themselves from future allegations of fraud by equivocating about the “efficacy” of their COVID-19 treatments. When directly questioned in December 2020 about the vaccine’s ability to limit transmission of the virus, Bourla offered casual, off-the-cuff replies such as, “I think that’s something that needs to be examined. We’re not certain about that right now.” His colleague, Ugur Sahin (co-founder and CEO of BioNTech), cagily couched his anticipatory optimism in these terms: “The first interim analysis of our global Phase 3 study provides evidence that a vaccine may effectively prevent COVID-19.” [my emphasis]The rest is history. When it later emerged, to the surprise of everyone whose understanding of the crisis was shaped exclusively by the Pfizer-sponsored mainstream media, that the company never even tested the shots for their ability to prevent transmission, gaslighting fact-checkers rushed to the defense of the executives. Why in the world would anyone ever have believed that the new vaccines would prevent transmission and infection?
The government-subsidized pharma giants succeeded in profiting enormously from the politically amplified crisis by persistently touting the efficacy of their products against a virus which 99+% of people were perfectly capable of surviving on their own. The shot salesmen claimed victory when injected persons did not die, when in reality most of them would have survived even if they had declined the treatment or been injected with an inert placebo instead. But the scheme ultimately worked because marketers (including public health authorities such as Anthony Fauci and Rochelle Walensky) unerringly referred to the shots as “vaccines,” a piece of sleight of hand made possible by the CDC’s own diluted redefinition of the term in 2021 to mean “a preparation that is used to stimulate the body’s immune response against diseases.” This linguistic legerdemain worked wonders to promote the new shots, when in fact the new definition is so broad and open-ended as to make it possible to label as a vaccine anything that strengthens the immune system, including leafy green vegetables, vitamins C and D, etc.
In retrospect, there can be no doubt that the populace and the politicians crafting policy all assumed that the labeling of the mRNA treatment as vaccines implied that the shots stopped transmission and infection, even while the savviest of the snake-oil salesmen evinced ignorance from the start about the most important question of all: whether these “vaccines” were indeed like all of the other vaccines, capable not just of “stimulating” the immune system, but of producing dependable and durable immunity.
Given the statistics now available, even the more modest claim, continually chanted by pharma marketers and their lackeys in the media, that the mRNA treatment greatly diminished severe illness and hospitalization, may have been false. For the death toll of COVID-19 victims increased rather than decreased in the year after the “vaccine” launch, and the countries with the worst vaccine uptake had some of the best outcomes. On top of the virus deaths, thousands of people were diagnosed with post-vaccine injuries of a variety of sorts, believed by many of them, their families, and at least some of their doctors to have been caused by the shots. Some of the vaccine injured ended up dying long before their time, and excess deaths were also caused by the disastrous political response to the virus, with fatal drug overdoses reaching record levels. Millions of persons missed vital health screenings, having been terrorized into believing that they could not leave their homes (much less enter COVID-19–infested health facilities!) without contracting something akin to the Black Plague. Among those who sought help for their ailments, some were flat-out denied treatment for acute illnesses, either because they were not dying specifically of COVID-19, or because they had refused the experimental treatment.
In coming to terms with what transpired over the past three years, it is helpful to bear in mind pre-2020 history. When the pharmaceutical industry’s newfangled psychotropic medications did not work as advertised, they created and blitz-marketed “add-on” drugs to increase the efficacy of antidepressants now known to have exhibited success in clinical trials on a par with placebos, but with far worse longterm adverse effects, up to and including addiction and suicidal ideation. Similarly, the slick pivot of the industry in response to the opioid catastrophe (caused by itself) was to launch and market drugs which could help people in the throes of narcotics addiction.
The flu shots marketed in collaboration with and subsidized by governments have been demonstrated in clinical trials to succeed on a par with placebos, while post-flu shot deaths are invariably written off as “coincidental.” Nonetheless, the industry capitalizes on the fact that they are starting anew each year—the previous year’s flu shot results being irrelevant to the next year’s projected success. As a result, when heavily lobbied and propagandized authorities impose mandates in some places (such as the State of Massachusetts), this may lead others to follow suit. Crony capitalist windfall profits ensure the ever-augmenting marketing budget of pharma firms, with the result that each subsequent year’s sales will exceed the previous year’s tally.
Given such precedents, no one should be surprised if the failure of the COVID-19 shots to prevent infection and transmission, or even to diminish the number of persons who died from the virus, does indeed end up serving as the pretext for governments to infuse even more money into research and development of new and what are promised once again to be “miraculous” cures to be used in the future. Not long after the launch of the COVID-19 vaccines, auxiliary treatments such as Pfizer’s Paxlovid and Merck’s Lagevrio were developed to treat people who became infected with the virus despite having been “fully” vaccinated. As clear evidence that many people’s capacity for critical thought continues to be compromised by fear, when legislation to rescind the utterly illogical and unscientific COVID-19 vaccine mandate on foreigners entering the United States made it to the floor of the House of Representatives, 201 Democratic congresspersons voted to keep the executive order in place.
The ongoing support of the official government pro-pharma narrative by the president, the press secretary, the defense secretary, and most Democratic members of Congress, even in the face of ample evidence (including post-vaccination positive COVID-19 tests) demonstrating that the shots did not diminish the incidence of infection is best explained by the fact that policymakers prefer not to own up to their mistakes. Ordinarily, individuals base their future actions on what they have learned from past experience. The question arises in the present circumstance: Why is there still a push for vaccine passports when the COVID-19 vaccines do not in fact confer immunity? The assumptions funding the push for universal vaccination continue to be embraced, as though the vaccines worked resplendently, despite an accumulation of scientific evidence to the contrary.
Now that Fauci himself has clearly explained why the mRNA technology will never offer a lasting solution to COVID-19, why would anyone, including Joe Biden and other advocates for the WHO (World Health Organization), still be in favor of implementing a universal health passport system regulating the movement of persons throughout the world? The current crop of shots do not offer longterm protection and do not moderate illness except in the case of persons in a very narrow cohort. Why require anyone to demonstrate that they participated in the experimental mRNA trial more than two years ago in order to be able to enter a country where the circulating variants bear little resemblance to the strain used to determine the formula of the first crop of vaccines?
There is no plausible health pretext available to explain why political leaders around the world would be keen to impose such a restrictive health passport program on free people, preventing them from traveling unless they first demonstrate their willingness to comply with future possible arbitrary orders decreed by public health authorities. That anyone not holding pharma stocks would support at this point the adoption of a health passport is best explained, again, by the politically induced trauma which appears to have psychologically scarred some persons for life. But just as the failure of the lockdowns to “stop the spread!” impelled leaders at every level of government—local, state, and federal—to prolong and intensify the lockdowns, those who pushed vaccine mandates will continue to press for universal vaccination passport requirements under the flatly false assumption that the reason why so many people died of COVID-19 was because of the evil antivaxxers who refused to comply.
What we are witnessing, the strangely intransigent push for vaccine passports, is entirely consistent with the comportment of the very persons who just succeeded in selling billions of shots. They will continue to insist that what we need to do is provide even more government funding to the pharmaceutical industry so that they can develop more and better cures for our ills. As disturbing as this may be, the most plausible explanation for the vigorous attempt to impose a health credential system on the people of the world is to provide the pharmaceutical industry with a limitless supply of not only customers, but also future experimental subjects.
As we have seen, the addition of the COVID-19 shot to the CDC’s immunization schedule for children—whose chances of dying from the virus are minuscule—serves only industry interests, by ensuring an endless crop of healthy young arms into which to inject the latest and greatest snake oils claimed to be panaceas (until it emerges that they are not). Likewise, the implementation of a universal health passport scheme restricting the motion of persons who opt not to undergo medical treatments of which they have no need would not only reap massive profits to the pharmaceutical industry but also represent the dawning of the pharma-techno state, in which citizens are subjects whose bodies are owned by their government.
The upshot here is that all of the pro-mRNA treatment propaganda and the incredibly vicious efforts to denounce and blame the noncompliant as the reason for the lengthy duration of the COVID-19 pandemic were nothing more than marketing ploys. That those who work behind the scenes of this well-oiled marketing machine were willing to destroy people’s relationships, their livelihoods, and in some cases even their very lives, reveals that their true motives were never to save the world from the virus but, instead, to profit from it. This is why we must resist any and all attempts by these same people and their toadies to foist upon us legal requirements to serve as guinea pigs in their future experimental trials, which is precisely what “health passports” would bring.
Laurie Calhoun is the Senior Fellow for The Libertarian Institute. She is the author of We Kill Because We Can: From Soldiering to Assassination in the Drone Age, War and Delusion: A Critical Examination, Theodicy: A Metaphilosophical Investigation, You Can Leave, Laminated Souls, and Philosophy Unmasked: A Skeptic’s Critique, in addition to many essays and book chapters. Questioning the COVID Company Line: Critical Thinking in Hysterical Times will be published by the Libertarian Institute in 2023.
A government-linked academic group pushed Twitter to censor factually correct stories about Covid-19 if they risked “fueling hesitancy” about vaccines, according to the latest batch of internal documents released by the platform’s new owner, Elon Musk.
Published by journalist Matt Taibbi on Friday, the documents show that from February 2021 onwards, senior Twitter management – including former trust and safety chief Yoel Roth – signed up to a Stanford University initiative that would alert them to the latest “vaccine-related disinformation narratives” spreading on the platform.
Titled ‘The Virality Project,’ the initiative was led by a former CIA employee and comprised academics from several universities, as well as researchers from organizations funded by the Pentagon, the National Science Foundation, and the US State Department. The Virality Project also stated on its website that it “built strong ties” with the Office of the Surgeon General, the Centers for Disease Control and Prevention, and the Department of Homeland Security, among other agencies and departments.
In its briefings to Twitter, the Virality Project recommended that “true content which might promote vaccine hesitancy” – such as stories of side effects and certain vaccines being banned abroad – be censored. Posts raising concern about vaccine mandates were viewed as “anti-vax” misinformation, while “just asking questions” was deemed “a tactic commonly used by spreaders of misinformation,” and posting about the “surveillance state” was deemed a bannable “conspiracy” theory.
It is unclear how often Twitter acceded to the Virality Project’s demands, though Taibbi said that within a month, the platform’s staff began using the project’s recommendations when evaluating content to censor.
At the time, Twitter’s rules on Covid-19 “misinformation” required a specific post to be “demonstrably false,” while permitting “strong commentary,” opinion writing, and satire. The Virality Project, however, urged Twitter management to ban “repeat offenders” before they even made new posts.
Sharing the leaked emails of White House coronavirus czar Anthony Fauci could “exacerbate distrust in Dr. Fauci and in US public health institutions,” the Virality Project warned in a June 2021 briefing, while a follow-up report highlighted the spread of “worrisome jokes” about harassing the door-to-door vaccine promoters deployed by the administration of US President Joe Biden.
“As Orwellian proof-of-concept, the Virality Project was a smash success,” Taibbi wrote on Friday. “Government, academia, and an oligopoly of would-be corporate competitors organized quickly behind a secret, unified effort to control political messaging.”
Since purchasing Twitter in October and installing himself as the platform’s new CEO, Musk has been releasing regular batches of internal documents and communications in a bid to shed light on its previously opaque censorship policies. A tranche of files released in December revealed that Twitter censored “legitimate content” on Covid-19 at the direct request of the White House.
The US Department of Defense funds private internet monitoring firms NewsGuard and PeakMetrics, which then trawl the web for “misinformation” to censor and demonetize, conservative news site The Federalist reported on Friday.
NewsGuard is a private company that rates news outlets by their “reliability” and reputation for sharing “falsehoods and misinformation narratives.” Before a Congressional hearing last week, journalist Matt Taibbi labeled the company a part of the “censorship-industrial complex,” publishing an image of a $750,000 grant award from the Pentagon to the firm. During the hearing, reporter Michael Shellenberger explained that NewsGuard uses its ratings system to drive advertiser revenue away from conservative sires or other “disfavored publications.”
In an email to Taibbi, Newsguard’s CEO Gordon Crovitz denied receiving government funding, stating instead that the government pays for access to its data. The Pentagon, he wrote, is specifically looking for evidence of “Russian and Chinese disinformation.”
However, NewsGuard received a $25,000 award from the Pentagon in 2020, after winning the military’s ‘Countering Covid-19 Disinformation’ challenge, The Federalist, a conservative news outlet, reported on Friday. A year later, Newsguard was given $750,000 to develop an AI-powered database of “misinformation networks” alongside the Department of Defense.
NewsGuard is one of several such businesses funded by the Pentagon. PeakMetrics was another winner of the Covid-19 challenge, earning a $25,000 grant to develop “social listening” technology for the military. It received a further $1.5 million from the federal government in 2021, but even before that the company had been singled out as potentially useful to the Pentagon.
In early 2020, PeakMetrics took part in the ‘Air Force Accelerator’ program, under which it developed “measuring tools to detect misinformation campaigns.” According to The Federalist, it put these tools to use during the 2020 and 2022 elections in the US. At that point, PeakMetrics solely worked for the US State Department and Pentagon, before later offering its services to the private sector.
It is unclear what the Pentagon aimed to achieve during these election monitoring campaigns. PeakMetrics did not respond to a request for comment by The Federalist.
Aside from paying private companies to develop web surveillance tools, the Pentagon, along with a number of other government agencies and departments, directly engaged in social media censorship in recent years. Internal communications from Twitter published by Taibbi, Shellenberger, and other journalists, showed that the social media giant “directly assisted” the US military’s online influence campaigns and censored “anti-Ukraine narratives” on behalf of multiple intelligence agencies. The platform also received extensive lists of accounts to ban from the US State Department and associated NGOs.
There has been a remarkable development to the story previously reported here.
Following that fiasco, I submitted a subject access information request to Elsevier (who publish The Lancet ) asking for all internal correspondence between editors and reviewers relating to the submission (and ultimate rejection) of our letter.
After a lengthy delay I received the response today. First their cover letter:
It is remarkable that most of the details are redacted even though it clearly is not done solely for the legitimate protection of the names of third parties. It is clear that I was being discussed in a negative light as they were referring to me as ‘an ongoing issue’. It is also clear that they only reached out after I publicised their initial delayed rejection letter on twitter (they were getting a lot of heat as a result of that).
It is disturbing to realise how much effort was spent in an attempt to ensure that an obviously flawed study promoting the Pfizer vaccine was not challenged.
Despite most of it being redacted there are still some alarming unredacted highlights (imagine what the redacted stuff says about us!) First they seem to reluctantly concede that I have a legitimate academic appointment:
In the following they mention ‘helpful background on Fenton’. Did they try to dig up dirt on me on their own or did the 77th brigade furnish them with my dossier?
They are worried about the close proximity of vaccine misinformation sources!
Next, they accuse me and (most likely) Martin Neil of retweeting ‘anti-vaxx posts on Twitter’. I’d be interested to know precisely who they are referring to and what posts:
They also refer to ‘holding off further email’ suggesting their offer to consider the letter was not genuine:
I am not happy about the scale of the redactions in the Elsevier response. If the Lancet editors were not making disparaging comments about me and colleagues, then there should be no reason to redact them. What do they have to hide?
The redactions suggest Elsevier have not acted in good faith, and neither have they acted in the spirit of FOIA.
Hence, I have informed Elsevier that if they are unable to provide a proper and full response with most of these comments unredacted, I will have no choice but to report them to the Information Commissioner’s Office (ICO).
This is not the first disgraceful episode in the recent history of the Lancet where, under Richard Horton’s leadership, clearly flawed papers promoting the ‘official narrative’ on covid have been published. Remember LancetGate when they published a fraudulent study that effectively stopped the use of hydroxychloroquine (HCQ) to treat covid patients. At least that paper was eventually retracted. In this case, rather than even allow a proper response to a flawed study, they have instead attacked their critics, accusing them of being spreaders of misinformation and ‘anti-vaxxers’.
It is worth noting that (as shown here), The Lancet is by no means the only major academic journal routinely rejecting any articles/letters that in any way question the accuracy of studies claiming vaccine effectiveness or safety. It is now fair to conclude that not a single major peer-reviewed study claiming vaccine effectiveness and/or safety can be trusted to be valid.
Role of supplementation is unclear. Prospectively study Associations, vitamin D supplementation and incident dementia N = 12,388 dementia-free people (from the National Alzheimer’s Coordinating Center)
Methods Baseline exposure to vitamin D was considered D+ No exposure prior to dementia onset was considered D− MCI and depression were both more frequent in the D− group, compared to D+ People taking vitamin D had less MCI and less depression
Adjusted for age, sex, education, race, cognitive diagnosis, depression, and apolipoprotein E (APOE) ε4. Potential interactions between exposure and model covariates were explored. Results Across all formulations, vitamin D exposure was associated with significantly longer dementia-free survival, and lower dementia incidence rate than no exposure
Hazard ratio = 0.60 (95% confidence interval: 0.55–0.65) Vitamin D exposure was associated with 40% lower dementia incidence versus no exposure. Over 10 year follow up of 12,388 2,696 participants progressed to dementia
Among them the 2,696 2,017 (74.8%) had no exposure to vitamin D 679 (25.2%) had baseline exposure
Exposure to vitamin D was associated with significantly higher dementia-free survival 5-year survival for D− was 68.4% 5-year survival for D+ was 83.6%
The effect of vitamin D on incidence rate differed significantly, Vitamin D effects were significantly greater in females versus males
Vitamin D effects were significantly greater in normal cognition versus mild cognitive impairment.
Vitamin D effects were significantly greater in apolipoprotein E ε4 non-carriers versus carriers.
Vitamin D effects were less significantly apolipoprotein E ε4 carriers. (25% one copy, 3% two copies)
Vitamin D has potential for dementia prevention, especially in the high-risk strata.
Vitamin D is known to participate in the clearance of amyloid beta (Aβ) aggregates, one of the hallmarks of Alzheimer’s disease (AD), and may provide neuroprotection against Aβ-induced tau hyperphosphorylation (neurofibrillary tangles) Cholecalciferol may be more effective than ergocalciferol
Recently, we have been touching on this theme of ivermectin as a treatment for cancer. So I was delighted to receive an excellent, well-researched piece on precisely this topic from an esteemed colleague. Dr Gérard Maudrux is a urology surgeon based in France and a strident champion for ivermectin. His article gives good insight into ivermectin’s mechanisms of action, while also acknowledging we have yet to discover them all.
I asked if I could share his article with you, and he graciously agreed. If you would like to read the original – in French – you can do so on Dr Maudrux’s blog.
Ivermectin and cancer: reserved for horses?
Dr Gérard Maudrux
Ivermectin is an extraordinary molecule, given its range of actions and safety. Since its discovery it has saved millions of lives, yet health authorities have relegated it to the status of a treatment reserved for horses; this is because medicines which are in the public domain threaten the pharmaceutical industry.
Here is a testimony received from a blog reader eight days ago:
“My wife is coming out of chemotherapy for advanced stage 3 ovarian cancer (the origin of my wife’s cancer is a mutation in the BRCA2 gene); after being assessed in the United States, she was treated with Taxol and Carboplatin.
Having read studies on the PNAS site (NB: Journal of the American Academy of Sciences ), that IVM associated with Taxol gave amplified results, I decided to supplement the chemo with 12mg of IVM every other day.
The first scan in July showed a large tumour and damage to the peritoneum. Laparoscopy confirmed the diagnosis. Ca125 marker assay = 288. From the start, I told my wife that COVID was still dragging on and that it would be useful to take ivermectin again, which had protected us from the epidemic, but which we had stopped taking in January.
After 3 chemo sessions (9 weeks), a new scan showed that the tumour was in strong regression with almost no trace on the peritoneum. Surgeon’s comment: it’s remarkable, I didn’t expect that. Ca125 dropped to 22! Operation decision within 15 days.
Uterus and ovaries were removed. Surgeon’s comment: this is extraordinary. No tumour, some dead cells on the peritoneum that I removed. The biopsy confirmed that everything has gone, Ca125 at 3.
The oncologist qualified the result as exceptional but that microscopic cells may remain, and so continued the chemo with Avastin from the 5th session. If I understand correctly, this treatment is to prevent the tumour from generating vessels to feed cancerous cells!!!! What tumour?
I informed them of my complementary “treatment” and shared my sources. Studies have shown that ivermectin restores apoptosis – this was of little interest: “I will look into it”. To this day I’m not sure they’ve done any research.”
Take note: this does not mean that ivermectin necessarily influenced this outcome – it may be a coincidence. Nevertheless this case should stand out, because this cancer is very nasty: peritoneal metastases indicate a very virulent and terminal cancer, with 87% mortality when at this stage, giving little hope.
Unfortunately, medicine as practiced in the 21st century gives this observation no value; it is not a randomized study at the cost of a few million. Moreover, no one will invest, since this molecule, which has fallen into the public domain, cannot be profitable. Observational medicine, which seeks to reproduce a possible discovery, no longer belongs in a world where industrialists and biostatisticians have replaced doctors.
It’s a shame, because ivermectin may have potential for actions that have not yet been explored. Besides its action on almost all parasites, its antiviral action proven by veterinarians and covered up in humans, its anti-inflammatory, immuno-regulatory, anti-cytokine shock action, but also its anti hemagglutination action that can protect against certain vascular side effects of vaccination, it is also clearly an adjuvant that reinforces certain anti-cancer treatments. I have also recently concluded that it is an anti-cancer treatment in its own right. It deserves twice its Nobel Prize.
Veterinarians are more advanced than doctors when it comes to the anti-cancer potential of ivermectin. This article from 2019, notes that ivermectin is more than an adjuvant, it is anti-carcinogenic, inhibiting the growth of mammary tumours in dogs – the most common kind in female dogs and with a poor prognosis. This is both in vitro and in vivo, stopping the growth of tumour cells.
This husband’s curiosity may have saved his wife’s life. It’s a shame that doctors are so unaware: this potential of ivermectin is not a recent discovery. But the authorities have done everything to belittle this extraordinary molecule because it is unprofitable.
In 2017, Santé Log and Top Santé covered a PNAS article referring to a study from the University of Osaka, reporting the anti-tumour effect of ivermectin on cancer cells of epithelial ovarian cancer, interacting with the KPNB1 gene responsible for the disease, with a direct effect on tumour apoptosis (programmed cell death which is the process by which cells trigger their self-destruction in response to a signal). Indeed, the KPNB1 gene behaves like an oncogene and the researchers confirm that its overexpression significantly accelerates the proliferation and survival of tumour cells, while its inhibition induces their apoptosis.
Ivermectin inhibits the activity of KPNB1 and has a synergistic effect combined with paclitaxel (Taxol), a standard drug for the treatment of epithelial ovarian cancer. The authors conclude: “we found that the combination of ivermectin and paclitaxel produces a stronger anti-tumour effect on EOC both in vitro and in vivo than either drug alone.” Taxol is also used in certain bronchopulmonary and breast cancers and in Kaposi’s sarcomas associated with AIDS. The synergy with ivermectin seen in ovarian cancer may be equally beneficial elsewhere.
This article in Pharmacologic Research studies the different mechanisms of action of ivermectin in different cancers, based on 114 studies. It states that “Ivermectin has powerful antitumor effects, including the inhibition of proliferation, metastasis, and angiogenic activity, in a variety of cancer cells…. ivermectin induces programmed cancer cell death, including apoptosis, autophagy and pyroptosis… ivermectin can also inhibit tumour stem cells and reverse multidrug resistance and exerts the optimal effect when used in combination with other chemotherapy drugs.”
They note this apoptosis with cells of ovarian cancer, colorectal, kidney, glioblastoma and leukaemia. Autophagy affects glioma, lung cancer and melanoma, and pyroptosis affects lung cancer cells.
Other articles study the action of ivermectin in colorectal and prostate cancer. Studies are underway for an injectable form of ivermectin, on breast, lung, bladder and melanoma cancers. Another notable work is a 2021 book on the repurposing of old molecules. The chapter on ivermectin recounts a number of experiments carried out on all these cancers.
Besides these potential effects on cancers, let’s not forget this other discovery from five years ago: remyelination, opening up avenues in the treatment of multiple sclerosis (here and here). Ivermectin has not finished surprising us.
Unfortunately for all of these applications, we will not see studies that lead to marketing authorization. Indeed, what is ivermectin at a dollar a tablet worth compared to treatments at a few thousand euros promoted by the major pharmaceutical groups?
As for medics who would prescribe this drug, knowing there are no harmful side effects even in the case of it not working, they will nevertheless be prosecuted. Rules are rules, it seems, and patients’ wellbeing is secondary.
Medicine is not moving in the right direction. Doctors don’t tend to like patients coming and asking for this or that examination or treatment, because they “saw it on the internet”. But if the doctors have thrown in the towel, surely this means someone else has to step up to the plate? It was not this husband’s job to read the medical articles that doctors should have read, but he was right to do so. I can’t help but liken this to reports of vaccine-related adverse events. In pharmacovigilance records, there are almost as many withheld statements made by patients as by health professionals.
It is not the role of patients and families to research treatments and report on their findings, but that of health professionals, many of whom seem to be AWOL. If we continue like this, in future it will be the patients treating the health providers! In the meantime, at least the horses will be well cared for.
I am frequently asked: why are the government agencies still pushing COVID-19 vaccination after there have been calls in the US Senate and all around the world to pull them off the market for lack of safety and efficacy?
In a March 10, 2023 letter from FDA Commissioner Robert Califf, MD, and CDC Director Rochelle Walensky, MD, MPH, to Florida Surgeon General Joseph Ladapo, MD, PhD, the agencies give their rationale. While Walensky does not have a compelling academic track record, her FDA counterpart Califf has been considered a staunch advocate of randomized trials and a hawk on safety of cardiovascular drugs over his career which was notable for building the Duke Clinical Research Institute, one of the most impressive academic research organizations in the world.
Here are 10 assertions that Califf and Walensky make to Ladapo and Americans on why the COVID-19 vaccines should be “pushed.”
“The claim that the increase of VAERS reports of life-threatening conditions reported from Florida and elsewhere represents an increase of risk caused by the COVID-19 vaccines is incorrect, misleading and could be harmful to the American public.” They are assuming unproven benefit at the start. The Bradford Hill criteria have been applied to VAERS and causality has been met. Autopsy studies have conclusively demonstrated causality for fatal syndromes. Doctors use the VAERS system when they believe COVID-19 vaccines caused the death, NOT when the death is unrelated to the vaccine in practice.
“The FDA-approved and FDA-authorized COVID-19 vaccines have met FDA’s rigorous scientific and regulatory standards for safety and effectiveness and these vaccines continue to be recommended for use by CDC for all people six months of age and older.” The FDA has relied on the false surrogate of antibody elevations after injection eight times. This is neither rigorous nor valid. Large randomized, double blind placebo controlled trials with hospitalization/death as the primary endpoint are required to prove efficacy in all age groups.
“Despite increased reports of these events, when the concern was examined in detail by cardiovascular experts, the risk of stroke and heart attack was actually lower in people who had been vaccinated, not higher.” They cite a nonrandomized study with inadequate control for the known determinants of cardiovascular disease. Both selection bias and confounding eliminate any valid claims of benefit. There is no mechanism by which COVID-19 vaccination would reduce cardiovascular events. There are >200 published manuscripts on COVID-19 vaccines mechanistically causing cardiovascular events including myocarditis, accelerated atherosclerotic cardiovascular disease, aortic dissection, hypertensive crisis, etc.
“FDA and CDC physicians continuously screen and analyze VAERS data for possible safety concerns related to the COVID-19 vaccines. For signals identified in VAERS, physicians from FDA and CDC screen individual reports, inclusive of comprehensive medical record review. Most reports do not represent adverse events caused by the vaccine and instead represent a pre-existing condition that preceded vaccination or an underlying medical condition that precipitated the event.” The agencies have not produced a report giving their analysis of what caused death after vaccination. Since many deaths occur on the day of the shot or in the next few days that follow, the public deserves to see regulatory evidence for cause of death.
“In addition to VAERS, FDA and CDC utilize complementary active surveillance systems to monitor the safety of COVID-19 vaccines.” CDC V-safe is one of the active systems mentioned. The CDC refused to release to the public until ordered by the courts, demonstrated an unacceptable 7-8% rate of hospitalization, emergency care, or urgent office visit caused by vaccine side effects. So agency use of systems demonstrate lack of safety and are not reassuring to the public.
“Based on available information for the COVID-19 vaccines that are authorized or approved in the United States, the known and potential benefits of these vaccines clearly outweigh their known and potential risks. Additionally, not only is there no evidence of increased risk of death following mRNA vaccines, but available data have shown quite the opposite: that being up to date on vaccinations saves lives compared to individuals who did not get vaccinated.” There are no randomized placebo controlled trials demonstrating hospitalization/death are reduced as primary endpoints. Thus the agencies cannot make an efficacy claim from a regulatory perspective. Nonrandomized studies have the following threats to validity: 1) selection bias—healthier more health conscious people take vaccines, 2) vaccinated are more likely to seek early treatment which reduces hospitalization/death, 3) no control over prior COVID-19 infection which greatly influences risk of hospitalization/death, 4) no adjudication of COVID-19 endpoints.
“Another study using mathematical modeling estimated that the vaccines saved an estimated 14 million lives from COVID-19 in 185 countries and territories between December 8, 2020, and December 8, 2021.” Modeling studies start with the unproven assertion that vaccination reduces death which has not been demonstrated in proper randomized trials, hence extrapolations to large populations are invalid.
“The most recent estimate is that those who are up to date on their vaccination status have a 9.8 fold lower risk of dying from COVID-19 than those who are unvaccinated and 2.4 fold lower risk of dying from Covid-19 than those who were vaccinated but had not received the updated, bivalent vaccine. Roughly 90% of deaths from COVID-19, as carefully classified by the CDC, in recent months have occurred among those who were not up to date on their vaccines.” This estimate did not account for the two known determinants of COVID-19 mortality: early treatment and natural immunity.
“Over the course of the pandemic, FDA and CDC have held numerous public meetings to discuss the safety and effectiveness of the COVID-19 vaccines where detailed safety data are shared with outside experts and public comment is encouraged. Further, FDA publishes the full regulatory action package containing hundreds of pages summarizing clinical studies and review for each COVID-19 approval on FDA’s website (see “COVID-19 Vaccines Authorized for Emergency Use or FDA Approved”) and CDC publishes an extensive amount of information on their clinical use in Interim Clinical Considerations. Complete information about both benefits and risks helps health care providers better care for their patients.” The FDA/CDC have never reviewed or commented on the Pfizer 90-day post-marketing data which reported 1223 deaths shortly after the shot. The FDA attempted to block these data to the public for 55 years. The agencies have never conducted a symposium to review the >1000 peer-reviewed published papers on serious adverse events and death after COVID-19 vaccination.
“Unfortunately, the misinformation about COVID-19 vaccine safety has caused some Americans to avoid getting the vaccines they need to be up to date.” The Rasmussen Report indicates 28% of Americans know someone who has died after the vaccine. Nothing in that report suggested “misinformation” was leading to hesitancy, moreover it was word of mouth on the horrifying outcomes Americans are witnessing among their family and friends that is leading to refusal rates of boosters.
There are easily another ten invalid assertions made by the agency that could be handled by experienced clinical investigators. Take a look at the letter yourself. Keep in mind the FDA/CDC deceived America by asserting that SARS-CoV-2 did not come out of the Wuhan Laboratory and just a few days ago the US House of Representatives voted to declassify our documents from the laboratory after multiple agencies and witnesses capitulated on the lab origin. This casts doubts on truthfulness of any agency public health assertions during the crisis.
The important message to Americans is that our agencies have no intention of carefully considering vaccine safety or changing course on their relentless pursuit of frequent, mass, indiscriminate COVID-19 vaccination down to 6-month old babies. It will be up to you to protect yourself and your family.
Prime Minister Benjamin Netanyahu has said that Israel felt threatened by Iran’s growing influence in the Middle East. Netanyahu expressed his Iranophobic view in a meeting with Russian President Vladimir Putin in Russia’s Black Sea resort of Sochi on Wednesday. Press TV has asked Scott Rickard, former American intelligence linguist from Tampa, Florida, and Brent Budowsky, a columnist at The Hill from Washington, to give their thoughts on the issue.
Rickard said Tel Aviv is concerned about the fact that the regime could not carry out its old project to spread sectarian divisions and pave the way for dismemberment of the countries in the Middle East region because of the Iranian-led resistance against Israeli policies, not only in the occupied territories of Palestine but also in the whole region.
“Iran is not a threat to Israel whatsoever. The threat that Israel sees is the fact that their Oded Yinon Plan is being put to a hold by Iran,” the intelligence linguist said on Thursday night.
“They (the Israelis) look at Iran as a threat only because they have no influence on their governments and Iran is autonomous and is not under the Zionist influence,” he added.
Since the victory of the Islamic Republic of Iran in 1979, Tehran has been critical of Israel’s policies in the region, whereas “no leaders [of other states] even dared to speak out against Zionism,” Rickard argued. … continue
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