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FDA Grants Full Approval of Moderna’s Spikevax COVID Vaccine — Another ‘Bait-and-Switch?’

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The U.S. Food and Drug Administration on Monday granted full approval of Moderna’s Spikevax COVID vaccine for people 18 and older. Similar to the agency’s licensing last year of Pfizer’s Comirnaty vaccine, the approval raised a number of legal questions.

By Michael Nevradakis, Ph.D.

Source: The Defender

The U.S. Food and Drug Administration (FDA) on Monday granted full approval of Moderna’s Spikevax COVID vaccine for people 18 and older.

Similar to the agency’s licensing last year of Pfizer’s Comirnaty vaccine, the approval raised a number of legal questions related to mandates and product availability.

Spikevax is a two-dose primary series, approved also for administration as part of a heterologous (“mix and match”) single booster dose for individuals who previously completed their original series of vaccinations with the Pfizer or Johnson & Johnson COVID vaccines.

According to the FDA, Spikevax “has the same formulation as the [Emergency Use Authorization (EUA)] Moderna COVID-19 Vaccine and … can be used interchangeably with the EUA Moderna COVID-19 Vaccine to provide the COVID-19 vaccination series.”

However, in its approval letter, the FDA said Spikevax is “legally distinct” from the Moderna EUA vaccine:

“The licensed vaccine has the same formulation as the EUA-authorized vaccine and the products can be used interchangeably to provide the vaccination series without presenting any safety or effectiveness concerns. The products are legally distinct with certain differences that do not impact safety or effectiveness.”

The FDA made the same distinction between the Pfizer-BioNTech EUA vaccine and the Pfizer Comirnaty vaccine, which the agency fully licensed in August, 2021, a move that raised questions about liability and the legality of vaccine mandates.

After Monday’s announcement, media outlets were quick to reassure the public the two Moderna vaccines are the same and that this was just a marketing ploy, where Moderna simply “rebranded” what is otherwise the same vaccine.

No ‘fully licensed’ COVID actually available

While Moderna’s Spikevax vaccine is now fully licensed, the original Moderna vaccine will remain under EUA. Indeed, the FDA on Jan. 7 reissued the EUA.

The FDA has also made it clear the Spikevax vaccine will not be available to the American public, announcing:

“Although SPIKEVAX (COVID-19 Vaccine, mRNA) and Comirnaty (COVID-19 Vaccine, mRNA) are approved to prevent COVID-19 in certain individuals within the scope of the Moderna COVID-19 Vaccine authorization, there is not sufficient approved vaccine available for distribution to this population in its entirety at the time of reissuance of this EUA.”

These claims parallel the chain of events that followed the FDA’s full approval of the Pfizer Comirnaty vaccine in August 2021.

At the time, Pfizer and the FDA claimed Comirnaty was not yet available, as there were sufficient stocks of the Pfizer-BioNTech EUA vaccine still available to be administered.

As of this writing, the FDA states, via its website, that Comirnaty products are “not orderable at this time.”

The FDA has not indicated when, or if, the Spikevax and Comirnaty vaccines will be available for distribution in the U.S.

Are EUA and fully licensed vaccines really interchangeable? 

As reported by The Defender, there is a significant legal distinction between products authorized under EUA and those fully licensed by the FDA.

EUA products are experimental under U.S. law. Under the Nuremberg Code and federal regulations, no one can force a human being to participate in this experiment.

Specifically, under 21 U.S. Code Sec.360bbb-3(e)(1)(A)(ii)(III), “authorization for medical products for use in emergencies,” it is unlawful to deny someone a job or an education because they refuse to be an experimental subject. Instead, potential recipients have an absolute right to refuse EUA vaccines.

That’s an issue military members, unable to find any vaccination sites that offer the fully licensed Comirnaty vaccine, cited in various lawsuits challenging vaccine mandates.

Notably, on Nov. 12, 2021, a federal judge rejected an argument by the U.S. Department of Defense, in defending the military’s vaccine mandate, that the Pfizer Comirnaty and Pfizer-BioNTech vaccines are “interchangeable.”

U.S. law also requires the EUA designation be used only when “there is no adequate, approved and available alternative to the product for diagnosing, preventing or treating such disease or condition.”

This means that, in legal terms, all EUA products should be withdrawn once alternative products have received full approval.

Perhaps the most significant legal distinction, however, pertains to the legal protections afforded vaccine manufacturers, depending on how their product is classified.

Under the 2005 Public Readiness and Preparedness (PREP) Act, EUA-approved vaccines enjoy a significant liability shield. Specifically, vaccine manufacturers, distributors, providers, and government officials involved in the policymaking, approval, and distribution process are immune from any legal liability.

Under such regulations, the only way an injured party can sue is if he or she can prove willful misconduct, and if the U.S. government has also brought an enforcement action against the party for willful misconduct.

No such lawsuit has ever succeeded.

Conversely, fully licensed vaccines, such as Spikevax and Comirnaty, do not have a liability shield, and are instead subject to the same product liability laws as other products.

This means the Spikevax and Comirnaty vaccines could expose pharmaceutical companies to significant financial claims if individuals injured by the vaccines chose to sue the vaccine makers.

The rush to get COVID vaccines authorized for all ages — a ploy to avoid liability? 

There’s another reason Pfizer and Moderna don’t want their fully licensed vaccines to be available yet — they’re waiting for the vaccines to be authorized, then licensed, for children as young as 6 months old.

Why? Because once a vaccine is fully licensed by the FDA, the only way its manufacturer can be shielded from legal liability is if the vaccine is added to the Centers for Disease Control and Prevention’s childhood vaccination schedule.

The National Childhood Vaccine Injury Act (NCVIA), passed into law in 1986, provides a legal liability shield to drugmakers if they receive full authorization for all ages and the vaccine is added to the mandatory schedule.

Reporting on the FDA’s approval of Spikevax, investigative journalist Jordan Schachtel wrote:

“Are Pfizer and Moderna waiting for full authorization for children’s shots to distribute Comirnaty and Spikevax to the masses? There’s plenty of litigators who have suggested that this is exactly what is going on in Big Pharma world.”

By creating the public perception that the Pfizer and Moderna EUA vaccines are fully approved, businesses, schools and other institutions are emboldened to impose vaccine mandates that violate existing law and allow the vaccines to be administered without informed consent.

It has also been argued that by relabeling the product, any previous data regarding vaccine injuries and side effects identified in association with the EUA vaccine are not counted in the safety studies for the approved vaccine.

The FDA approval of the Pfizer Comirnaty vaccine, its subsequent lack of availability and the continued administration of the Pfizer-BioNTech EUA vaccine led Children’s Health Defense (CHD) to file a lawsuit against the FDA and its acting director, Dr. Janet Woodcock, for their allegedly deceptive and rushed approval of the Comirnaty vaccine, arguing that the approval represented a classic “bait and switch” tactic.

CHD further alleged in its lawsuit that the FDA violated federal law when it simultaneously licensed Pfizer’s Comirnaty vaccine and extended Pfizer’s EUA — as the agency has now done with Moderna and Spikevax — for a vaccine that has the “same formulation” and that “can be used interchangeably,” according to the FDA.

FDA admits no safety data for Spikevax use among pregnant women

Beyond the legal questions raised by the FDA’s approval this week of Spikevax, the approval also raises safety questions.

For instance, the FDA admitted Spikevax was insufficiently tested on pregnant women, stating that “[a]vailable data on SPIKEVAX administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy.”

Furthermore, Spikevax was approved without having been tested for its ability to provide protection against the Omicron variant, which is reported to account for 99.9% of current U.S. COVID cases — it was approved only for providing protection against mutations that are no longer circulating.

And yet, the FDA cited the Omicron variant as the reason behind its decision to pull its EUA for monoclonal antibody products. The FDA claims that these products have not been shown to provide protection against the Omicron variant.

Crimes against Our Country

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By James Howard Kunstler

Source: Kunstler.com

The year of sickening global psychosis ended with virologist and vaccine-uberspecialist Dr. Robert Malone truth-bombing the Internet with three hours of straight talk about the US health authorities’ campaign to destroy the lives of at least half a million US citizens (so far) and, leading by example, to harm multiples of that number of innocent people across all of Western Civilization. Podcaster Joe Rogan assisted skillfully in an interview that is finally rocking the world out of an epic consensus trance. (Listen.)

By health authorities I don’t just mean Dr. Anthony Fauci, the designated National SARS-CoV-2 Coordinator, or his accomplices in the Dept. of Health and Human Services agencies, CDC, NIH, NIAID, etc., but also the purblind US medical establishment of actual doctors in clinical practice, researchers, hospital administrators, and pharma executives who acted with a collective stupid malevolence not seen since the crematory-stuffers of the Nazi bureaucracy carried out their final solution.

We know what you did. You engineered and patented a gain-of-function virus at the same time you conspired with pharma companies to devise and patent pseudo-vaccines, and then you loosed both of them on the public. You didn’t just fail to adequately test the “vaccines” cooked up by Moderna, Pfizer, and Johnson & Johnson, but you deliberately botched the trails and lied about it. You created rich $$ incentives for hospitals to mis-treat Covid patients by failing to use known, safe, effective anti-virals. You conspired with social and news media to suppress information about those common anti-viral drugs that would have informed many patient’s decisions and saved thousands of lives. You treated late-stage patients dying of Covid-induced vascular disorder with the ineffective and toxic drug remdesivir that Dr. Fauci had developed unsuccessfully for an ebola outbreak years ago. (Nurses turned so cynical about the remdesivir protocol that they nicknamed it “run-death-is-near.”) You prompted government officials to lockdown society, force useless masking, and now to coerce “vaccination” by threatening to deprive citizens of their livelihoods.

The US Supreme Court will entertain arguments this Friday, January 7, to enjoin against “Joe Biden’s” mandates to coerce “vaccination” in companies that employ more than a hundred people and a separate mandate forcing vaxxes on staff at Medicare / Medicaid certified “providers” (meaning most hospitals and doctors’ offices). There’s a pretty good chance the court will decide against the mandates. They’re expected to rule Monday, January 10, the day that the mandates are supposed to take effect.

The government’s actions around the Covid-19 event look more and more to be deliberately and maliciously intended to harm lives and cause social and economic breakdown. In the last weeks of 2021, federal public health officers even blocked shipments of monoclonal antibodies around the country, despite their proven efficacy. The CDC scheduled the use of PCR tests for Covid-19 to end on December 31, after declaring them unreliable in August. Why the five-month lag? (To keep case numbers jacked up, that’s why.)

Every effort is being made to extend emergency use authorizations for unsafe and ineffective “vaccines” in order to sustain shields against liability for the benefit of their manufacturers. Pfizer refuses to release in the USA its FDA-approved comirnaty version of the EUA-protected BioNTech product for that reason. The Pentagon has lied and confabulated its use of the two Pfizer products in order to illegally force unapproved BioNTech vaccinations on enlisted men and women. Hospital directors, doctors, and their professional associations continue to persecute colleagues who speak publicly against the “vaccines.” The “vaccine” makers refuse to disclose the exact contents of their products, and were permitted to withhold data on safety trials until a half-century into the future. The obvious conclusion is that they don’t want the public to be informed about any of this. The net effect is that medicine in the USA has destroyed its own authority. Who can trust his doctor knowing that they’ve gone along with all this epic dishonesty?

The country is heading into an agonizing reality-test at a scale and speed never seen before in world history. You can already assume that government has lost control of the Covid-19 story. The Omicron scare is failing miserably. Lots of cases, few deaths, mild symptoms. Government’s credibility is shot. In the months ahead, we’ll learn just how harmful those “vaccines” were — especially among American children — as deaths mount from damage done to people’s organs and immune systems.

The perfidious news media is scrambling now to adjust its narratives, but they won’t escape the record of falsehood they’ve sedulously laid down. They can’t delete or rewrite every story in their archives, and many of these are printed out in hard-copy anyhow. Next, they’ll try apologizing. (“Sorry, but the pandemic drove us a little nuts.”) That’s hardly enough. They have to answer in courts of law — or else we must just declare the USA a lawless state.

The Covid-19 crimes against our fellow citizens amount to only one piece of a package of reality-tests coming our way in 2022. Do you think Special Counsel John Durham skulked off to drink pina coladas in oblivion after indicting a couple of errand boys (Danchenko and Sussman)? He is a hypersonic force orbiting over a well-known cast of political criminals who are headed for prosecution. Next up will be the train wreck of the US economy. Do you think the crimes around the 2020 national election are buried and forgotten? You’re in for some harsh surprises. Things have truly flipped. You just don’t realize it yet.

Malfeasance Behind the FDA Vax OK for Children

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By F. William Engdahl

Source: New Eastern Outlook

On October 27 the US Food and Drug Administration Advisory Panel on Vaccines recommended the agency allow Pfizer to amend its Emergency Use Authorization for its COVID vaccine to include children 5 through 11 years old. Two days later the FDA officially approved the rollout. Major media are treating this as a positive development to protect young children. On closer inspection it is anything but that. The FDA is today shockingly corrupt under the Acting Director and is little more than a rubber stamp for Big Pharma, and especially Pfizer, where the former FDA head sits on the board.

The FDA’s Vaccines and Related Biological Products Advisory Committee voted 17 to 0, with one abstention, to give a green light allowing Emergency Use Authorization for the Pfizer-BioNTech experimental mRNA to children between 5 and 12 years. The expert who abstained later explained he did so because of limited safety and efficacy data provided. Previously the FDA had approved the vaccine for 12 and older. Adding to the stench of corruption around the latest vote, the Biden Administration a week earlier announced it had already purchased enough Pfizer vaccine to inoculate all 28 million 5- to 11-year-olds in the US. Did they know the fix was in?

‘…Just the Way it Goes’

The record of the FDA, the major drug oversight agency in the US Government, regarding safety and risks of the experimental gene-altered mRNA vaccines of Pfizer, is one of criminal malfeasance, defined as willful violation of a public trust or obligation that causes harm or death. Their latest ruling is even more egregious for blatant conflicts of interest and scientific fraud. Both Pfizer, who conducted the tests on the efficacy of their own vaccine on the 5-11 year age group, and the FDA experts, admitted that they had no idea if the vaccine was safe for such a young population.

Dr. Eric Rubin, professor of immunology at the Harvard T.H. Chan School of Public Health voted to approve the Pfizer-BioNTech vaccine, noting, “The data show that the vaccine works and is pretty safe … and yet we’re worried about a side effect that we can’t measure yet, but it’s probably real.” That is hardly confidence-building. He then stated, “we’re never going to learn about how safe this vaccine is unless we start giving it. That’s just the way it goes.”

This cold-blooded nonchalance is even more astonishing in light of the fact that the incidence of serious side effects in the 5-11 age group who allegedly have tested positive for the corona virus is essentially zero. According to data of the US Government Centers for Disease Control, the Infection Fatality Rate for children from 0-17 years is 0.0002 per 100,000 and far lower for the 5-11 years. A research study by Johns Hopkins University found that risk of severe illness or death from covid19 in a study of 48,000 children is essentially zero if no other morbidity risk such as leukemia, diabetes or asthma is present. Moreover, risk of infecting other children is also very low.

In their submission to FDA for approval, Pfizer stated the vaccination was needed for the 5-11 age group to prevent covid disease transmission. Yet in their FDA hearing on questioning, Dr. William Gruber, senior vice president of Pfizer Vaccine Clinical Research and Development, said they did not even assess whether the vaccine prevents transmission. We might ask why is this at all needed then if the risk to children is zero and there is no evidence of children transmission?

Even more shocking is the statement by Pfizer about its tests. First there were no animal tests on rats or such first. They admitted that the tested human group was so small that they could not test for myocarditis or pericarditis. Yet those are among the most reported negative effects for all others that have had the Pfizer jab. In its FDA application Pfizer noted that the number of participants in the current clinical development program was “too small to detect any potential risks of myocarditis associated with vaccination,” and that “to evaluate long-term sequelae of post-vaccination myocarditis/pericarditis” in participants 5 to <12 years of age will not be studied until after the vaccine is authorized for children.”

Flawed Pfizer Tests

The tests Pfizer made were also fatally flawed. According to Dr. Josh Guetzkow, of the Hebrew University of Jerusalem, the Pfizer study was not double-blind. Further, Pfizer cherry-picked subjects to evidently better their results. Three thousand children age 5-11 received Pfizer’s COVID vaccine, but only 750 of those children were selectively included in the company’s safety analysis. And Pfizer dismissed cases with adverse vaccine effects in their FDA filing: “Few serious Adverse Events, none of which were related to vaccine, and no AEs leading to withdrawal were reported.” They give no explanation how that was determined. Just trust Pfizer.

And post-vaccination follow up was less than 2 months for one test cohort and only 2.4 weeks for a second. The Pfizer report to FDA read, “Supplemental safety expansion group data were analyzed from approximately 1500 vaccine recipients with a median follow-up time of 2.4 weeks after Dose 2. These supplemental data demonstrate an acceptable safety profile…” It can take months or longer for side effects to manifest. Vaccine experts recommend at least 18-24 month post-vaccine follow up, not 3 months or 2.4 weeks. This is not serious science.

As well, it seems the FDA and or Pfizer wrongly name the vaccine in the title as “BNT162B2 [COMIRNATY (COVID-19 VACCINE, MRNA)] .“Yet the actual FDA text calls it “Pfizer-BioNTech COVID-19 Vaccine (BNT162b2).”

The separate company, BioNTech of Mainz, Germany, has a similar but “legally different” vaccine, trade-named Comirnaty, that is not available in the USA. The distinction is essential as it was the basis in August for the corrupt FDA to give Pfizer-BioNTech vaccine an extension of Emergency Use Authorization but to misleadingly declare its full approval for Comirnaty vaccine of BioNTech. This is deliberate fraud and allowed the Biden Administration to mandate vaccination of US government workers (curiously except for White House and Congress), military, and any company with more than 100 employees.

Conflicts of Interest?

The corruption of the FDA extends to the members of the Vaccine Advisory Committee. Many of the members of the current 18 person committee have direct ties to Pfizer or to the pro-Pfizer Gates Foundation.

Prof. Holly Janes of the Fred Hutch Cancer Research Center in Seattle designed the flawed Pfizer tests. Her institute is funded by Gates Foundation money. FDA committee member Dr. Steven Pergam is also with the Gates-funded Fred Hutch center. Acting committee chair, Arnold S. Monto was a paid consultant to Pfizer. Committee member Archana Chatterjee worked on a Pfizer research project related to vaccines for infants between 2018-2020. Geeta K. Swamy is chair of the “Independent Data Monitoring Committee for the Pfizer Group B Streptococcus Vaccine Program,” a committee sponsored by Pfizer. Duke University states that “Dr. Swamy serves as a co-investigator for the Pfizer COVID-19 vaccine trial.” FDA Committee member Gregg Sylvester was a vice president for Pfizer Vaccines. Ofer Levy, professor of pediatrics at Harvard Medical School is on record vigorously supporting Pfizer covid vaccines for children 12 and older. And FDA committee member Paul Offit professor of pediatrics at The Children’s Hospital of Philadelphia called openly last June for covid vaccine permission for children.

When we compare the actions of corrupt FDA Acting Director Janet Woodcock during the August FDA extension of emergency use authorization for Pfizer-BioNTech vaccine, she refused then to even allow the vaccine committee to meet to debate the issue. Several months before in June 2021 three members of the FDA Vaccine Committee resigned in protest over Woodcock’s refusal to heed the near unanimous vote of the advisory committee to approve an Alzheimer’s drug called Aduhelm against the wishes of nearly every member on the panel.

Clearly Woodcock has been busy in the meantime stacking the advisory committee with pro-Pfizer members. Not to be forgotten is the fact that after he left as head of the FDA under Trump, Scott Gottlieb immediately joined the board of directors of…Pfizer Inc. Woodcock served under him at FDA.

Woodcock has been at FDA since 1986, almost as long as Fauci at NIAID. Woodcock was Biden’s choice to head FDA, but a massive opposition from 28 groups including state attorneys general and citizen groups forced him to name her “acting,” which does not need Congressional scrutiny. Woodcock was directly responsible for the original FDA approval of deadly opioids over the objections of her own scientists and other advisors.

Already California has moved to make public school admission contingent on covid vaccination, anticipating Pfizer approval. This spread of the deadly Pfizer vaccine to children who have near zero risk of serious disease makes no public health sense. It is simply prima facie evidence of medical malfeasance at the highest levels of the US Government including FDA, with plausible criminal intent. The FDA decision will now be used to argue for similar inclusion of essentially no risk children for the vaccine jab.

It All Makes Sense Once You Realize They Want to Kill Us

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By Mike Whitney

Source: The Unz Review

“It is now apparent that these products in the blood stream are toxic to humans. An immediate halt to the vaccination programme is required while an independent safety analysis is undertaken to investigate the full extent of the harms, which the UK Yellow Card data suggest includes thromboembolism, multi-system inflammatory disease, immune suppression, autoimmunity and anaphylaxis, as well as Antibody Dependent Enhancement (ADE).” Tess Lawrie, Evidence-Based Medicine Consultancy

“For we wrestle not against flesh and blood, but against the rulers of the darkness of this world, against spiritual wickedness in high places.” Ephesians 6:12

Question– Have the mRNA vaccines been tested on animals?

Answer– Yes, they have.

Question– Were the animal trials successful?

Answer– Yes and no.

Yes, the experiments on mice showed that a low dose of the vaccine induces a robust antibody response to the infection.

But, no, the antibodies were not able to attack the spike protein from a different strain of the virus.

Question– I’m not sure what that means? Do you mean that the vaccine DOES provide some limited protection from the original (Wuhan) virus, but does not necessarily provide protection from the variants?

Answer– That’s right, but it’s a bit more complicated than that because– as the virus changes — the antibodies that helped to fight the original virus can actually enhance the “infectivity” of the variant. In other words, vaccine-generated antibodies can switch-sides and increase the severity of the illness. Simply put, they can make you sicker or kill you. Scientists have known this for a long time. Check out this clip from a 2005 research paper:

“A jab against one strain might worsen infection with others….

In the.. study, Gary Nabel of the National Institute of Allergy and Infectious Diseases.. injected mice with spike protein from a SARS virus taken from a human patient infected in early 2003. They then collected the antibodies the animals produced.

In lab experiments, they showed that these antibodies were unable to attack spike protein from a different strain of SARS, isolated from a patient infected in late 2003….The team next tested whether the antibodies would attack spike proteins from two SARS strains isolated from civets, from which the virus is thought to have originally jumped into humans. In this case, they found hints that the antibodies actually boosted the ability of the virus to infect cells.…

The results show that the virus changes over time, so that a strain that crops up in one outbreak might be quite different from that in a later outbreak. “This virus is not standing still and we need to take this into account,” Nabel says.

This raises the prospect that a vaccine against one strain of SARS virus could prove ineffective against others. Worse, a jab against one strain might even aggravate an infection with SARS virus from civets or another species. “It’s obviously a concern,” Nabel says..
This would not be the first case where exposure to one strain of a virus can worsen infection with another.” (“Caution raised over SARS vaccine”, Nature)

Question– I’m still confused. Can you summarize what they’re saying?

Answer– Sure. They’re saying that scientists have known for nearly two decades that vaccines narrowly aimed at just one protein are bound to fail. They’re saying that the spike protein is highly-adaptable and capable of changing its shape to survive. They’re saying that vaccines aimed at the spike protein will inevitably produce variants that evade vaccine-generated antibodies. They’re saying that by narrowing the vaccine’s focus to the spike protein alone, the drug companies have ensured that previously helpful antibodies will do an about-face, allow the virus to enter healthy cells, replicate at will, and cause sickness or death. They are saying that the current crop of vaccines is in fact perpetuating the pandemic. And–since the science has been clear for the last 16 years– we can add one more observation to the list, that is, that the current approach to mass vaccination is neither haphazard, slapdash or random. It is intentional. The vaccination campaign managers are deliberately ignoring the science in order to sustain a permanent state of crisis. Science is being manipulated to achieve a political objective.

Question– I think you’re exaggerating, but I’d like to get back to the animal trials instead of arguing politics. As you probably know, the reports in the media do not square with your analysis, in fact, all of the articles in the MSM say the animal trials were a rousing success. Here’s a short blurb that I found today that confirms what I’ve been saying:

“…vaccination of nonhuman primates with the mRNA vaccine induced robust SARS-CoV-2 neutralizing activity and notably, rapid protection in the upper and lower airways….” (Covid-19, NIH.gov)

Question– Are you suggesting the authors are lying?

Answer– No, they are not lying. They’re just not telling you the whole truth, and you need to know the whole truth so you can make an informed decision. The vaccines DO provide some (temporary) protection. We don’t dispute that. They also trigger a strong immune response. We don’t dispute that either. But what difference does it make? Let me explain: Let’s say, you have a really bad head cold so you take a new medication that you think will relieve the pain. And–sure enough– an hour after taking the pills– Presto — your congestion and headache are completely gone. That’s fantastic, right? Wrong, because what you fail to realize is that the medication is laced with slow-acting strychnine that kills you three days later. Do you still think it was a good idea to take the medication?

Of course, not. And the same rule applies to these vaccines which do, in fact, boost your antibodies and provide some fleeting “immunity”. But they can also kill you. Don’t you think that should be factored in to your decision? Keep in mind, people have died 3, 4, 5 weeks after inoculation without any prior warning. Many of them might have even been bursting with antibodies, but they’re still dead. Can you see the problem?

Question– Okay, but there’s still this matter about the animal trials. The media says that the drug companies performed the animal trials and they were successful. Do you disagree with that?

Answer– They were not successful and the “fact checkers” that were hired to discredit vaccine critics like me, have deliberately mischaracterized what happened in the trials. For example, here’s a typical “fact checker” article titled “COVID-19 vaccines did not skip animal trials because of animal deaths” by Reuters. Here’s an excerpt:

“Posts claiming that COVID-19 vaccine producers skipped animal trials due to the animals in those trials dying are false. Pfizer-BioNTech, Moderna and Johnson & Johnson, which have been granted emergency authorization use by the Food and Drug Administration (FDA) in the United States, all conducted animal trials and had no significant safety concerns to report.”

Sounds reassuring, right? But then they say:

“Due to time constraints and the urgency to find a vaccine for COVID-19, Moderna and Pfizer did receive approval to run animal testing and early trials on humans at the same time, as opposed to fully completing animal trials before moving on to human trials. This, however, does not mean animal trials were skipped or that the safety of the vaccines were compromised.”

Let me see if I got this straight: The drug companies were in such a hurry that they conducted their minimalist animal trials at the same time as their human trials (which is unprecedented) and then rushed the results to the FDA so they could be rubber stamped and waved through under the Emergency Use Authority?

Is that how it went down?

Yes, it is.

But if they were rushed through in a couple months, then the “fact checkers” are tacitly admitting that there is no long-term safety data. And there IS no long-term safety data, nor is there any attempt to disprove the research from the earlier trials where the ferrets, mice and other animals died following injection of mRNA vaccines. They don’t deny it, they just ignore it as if sweeping it under the rug will make it all go away. Here’s a clip from the research paper that Reuters refers to in its article:

“We demonstrate that the candidate vaccines… respectively—induce strong antigen-specific immune responses in mice and macaques….Both (vaccines) protected 2–4-year-old macaques from challenge with infectious SARS-CoV-2, and there was reduced detection of viral RNA in immunized macaques as compared to those that received saline.” (Note–We’ve already acknowledged that the vaccines do produce a strong immune response. Here’s more:)

“Neutralizing GMTs declined by day 56 (35 days after dose 2), consistent with the contraction phase; however, they remained well above the GMT of the human sera panel. The duration of the study was not long enough to assess the rate of decline during the plateau phase of the antibody response.” (“BNT162b vaccines protect rhesus macaques from SARS-CoV-2”, Nature)

Can you see what’s going on? The trial was only 56 days-long, in fact, none of the animal trials exceeded 56 days. Think about that for a minute. The reason the animals died in prior trials is because they were exposed to a mutated version of the (wild) virus that eventually killed them. That’s how ADE (antibody-dependent enhancement) works. It doesn’t happen overnight and it doesn’t happen in 56 days. It takes much longer than that for a mutated version of the virus to emerge and reinfect the host. The drug companies know that. They’re not stupid. So the fact that the animals mounted a strong immune response is completely irrelevant. We KNOW they mounted a strong immune response. We also know they died some months later when a different strain of the virus emerged. Bottom line: The production of antibodies does not mean a drug is safe.

The obvious purpose of the trials was to get the vaccines over the finish-line before anyone figured out what was going on. It’s the same reason why the drug companies “unblinded” their human trials after the vaccines got the green light from the FDA. Shortly after the trials were concluded, the people in the placebo arm were allowed to get vaccinated.

Why would they do that? Why would they vaccinate the people who willingly allowed themselves to be guinea pigs for the sake of public health, only to vaccinate them shortly after, thus, eliminating any chance of finding out what the long-term safety issues might be? It makes no sense, does it?

Take a look at this short clip from the British Medical Journal whose scientists are equally bewildered:

“The (drug) companies say they have an ethical obligation to unblind volunteers so they can receive the vaccine. But some experts are concerned about a “disastrous” loss of critical information if volunteers on a trial’s placebo arm are unblinded…

Although the FDA has granted the vaccines emergency use authorization, to get full license approval two years of follow-up data are needed. The data are now likely to be scanty and less reliable given that the trials are effectively being unblinded.

Consumer representative Sheldon Toubman, a lawyer and FDA advisory panel member, said that Pfizer and BioNTech had not proved that their vaccine prevents severe covid-19. “The FDA says all we can do is suggest protection from severe covid disease; we need to know that it does that,” he said.

He countered claims, based on experience with other vaccines, six weeks of follow-up was long enough to detect safety signals. Six weeks may not be long enough for this entirely new type of “untested” [mRNA] vaccine, Toubman said.

Goodman wants all companies to be held to the same standard and says they should not be allowed to make up their own rules about unblinding. He told The BMJ that, while he was “very optimistic” about the vaccines, “blowing up the trials” by allowing unblinding “will set a de facto standard for all vaccine trials to come.” And that, he said, “is dangerous.”

(“Covid-19: Should vaccine trials be unblinded?” The British Medical Journal)

Do you like his choice of words: “blowing up the trials”? Do you think it is a fair description of what the drug companies did?

Yes, it is.

And what possible motive would the drug companies have to blow up the trials? I can see only two possibilities:

  1. They think their vaccine is so terrific, it will save the lives of many of the people in the placebo group.
  2. They expect a high percentage of the people in the vaccine group to get either severely sick or die, so they want to hide the evidence of vaccine-linked injury.

Which is it?

You know the answer. Everyone watching this farce knows the answer.

Question– Okay, so let’s cut to the chase: Are the vaccines are safe or not?

No, they are not safe. The way we decide whether a drug is safe or not is by putting it through a rigorous process of testing and clinical trials. After the testing, the data is passed on to physicians, statisticians, chemists, pharmacologists, and other scientists who review the data and make their recommendations or criticisms. That didn’t happen with the Covid vaccines, in fact, all the normal standards and protocols were suspended in the name of “urgency”. But many believe that the “urgency” was manufactured to push through vaccines that would never have been approved on their own merits. All you have to do is look through the vaccine injury data (VAERS) and you’ll see this is the most lethal medical intervention of all time and, yet, the public health experts, the media and the government keep crowing that they’re “safe and effective”. It’s nonsense and the drug companies know it’s nonsense which is why they reject all liability for the people that are going to be killed by these “poison-death shots.”

Do you know what goes on inside your body after you are injected with one of these “gene based” vaccines?

Once the vaccine enters the bloodstream it penetrates the cells that line the blood vessels forcing them to produce spike proteins that protrude into the bloodstream like millions of microscopic thorns. These thorns activate blood platelets which trigger blood clotting followed shortly after by an immune response that destroys the infected cells thus weakening the vascular system while draining the supply of killer lymphocytes. In this way, the vaccine launches a dual attack on the body’s critical infrastructure causing widespread tissue damage throughout the circulatory system while leaving the immune system less able to fend off future infection.

Now if you think you can have a long-and-happy without a functioning circulatory system, then none of this matters. But if you’re bright enough to realize that wreaking havoc on your vascular system is the fast-track to the graveyard, then you’ll probably understand that injecting these “poison-death shots” is a particularly bad idea.

By the way, it’s a real stretch to call these hybrid injections, “vaccines”. They have about as much in common with a traditional vaccine as a python does with a coffee table. Nothing. The “vaccine” moniker was chosen in order to shore-up public confidence, that’s all. It’s part of a marketing strategy. There is no real similarity. The majority of people trust vaccines and see them as a shining example of medical achievement. The drug companies wanted to tap into that trust and use it for their own purposes. That’s why they called it a “vaccine” instead of “gene therapy” which more accurately describes ‘what it does.’ But–like we said– it’s just a marketing strategy.

Have you ever wondered how the drug companies were able to roll out their own-individual vaccines just weeks apart from each other? That’s a pretty good trick, don’t you think; especially since vaccine development typically takes from 10 to 15 years. How do you think they managed that? Here’s an excerpt from an article which provides a little background on the topic:

“The virus behind the outbreak that began in Wuhan, China, was identified on Jan. 7. Less than a week later — on Jan. 13 — researchers at Moderna and the NIH had a proposed sequence for an mRNA vaccine against it, and, as the company wrote in government documents, “we mobilized toward clinical manufacture.” By Feb. 24, the team was shipping vials from a plant in Norwood, Mass., to the National Institute of Allergy and Infectious Diseases, in Bethesda, Md., for a planned clinical trial to test its safety.” (“Researchers rush to test coronavirus vaccine in people without knowing how well it works in animals”, Stat)

Got that? “The virus broke out in Wuhan…on Jan. 7, and less than a week later Moderna had a proposed sequence for an mRNA vaccine against it???

Really? Is that the same Moderna that had been playing-around with mRNA for over a decade but was never able to successfully bring a vaccine to market?

Yep, the very same company. Here’s more:

“And by Feb. 24, the team was shipping vials from a plant in Norwood, Mass??”

Wow! Another Covid miracle! You almost get whiplash watching these companies crank out their “wonder drugs” at record-breaking speed.

Keep in mind, there’s a very high probability that the virus was man-made, (In other words, it’s a bioweapon.) and the people who have been implicated in the funding and creation of that bioweapon are also closely aligned with the big drug companies that have produced the antidote in record time that has already netted tens of billions of dollars in profits for a drug for which there was no reliable animal testing, no long-term safety data, and no formal regulatory approval.

So I’ll ask you again: Doesn’t that all sound a bit suspicious?

Is it really that hard to see the outline of a political agenda here? After all, aren’t the drug companies working with the regulatory agencies that are working with the public health officials that are working with the media that are working with the corrupted politicians that are working with the Intel agencies that are working with the meddling globalist billionaires that are working with the giant private equity firms that oversee the entire operation pulling the appropriate strings whenever needed?

It sure looks like it.

And, don’t the tectonic social changes we’ve seen in the last year have more to do with a broader scorched-earth campaign launched by the “parasite class” against the rest of humanity than they do with a fairly-mild virus that kills mainly old and frail people with multiple underlying health conditions?

Right, again. In fact, many have noticed the cracks in the pandemic artifice from the very beginning, just as many have pointed out that the virus-meme is just the mask behind which parasites continue to conduct their global restructuring project. In short, it’s all about politics; bare-knuckle, take-no-prisoners NWO politics.

Answer– You’ve asked a number of questions about the animal trials, but none about the biodistribution and the pharmacokinetics studies that were done at the same time. Why is that? (Note--Pharmacokinetics; “the branch of pharmacology concerned with the movement of drugs within the body.”)

Question– I didn’t know there were any. Did the media report on them?

Answer– No, they didn’t. They completely ignored them, even though they were produced by Pfizer and provide essential information about where the substance in the vaccine goes in the body, in what amounts, and for how long. By knowing how the drug is distributed, it is possible to make educated assumptions about its effect on the organs and other tissue. In other words, these studies are invaluable. The Doctors for Covid Ethics have done extensive research on the studies and written a report titled “The Pfizer mRNA vaccine: pharmacokinetics and toxicity”. Here’s a few excerpts that help to illustrate the dangers of the vaccines:

“As with any drug, a key consideration for the toxicity of the COVID mRNA vaccines is where exactly in the body they end up, and for how long they will stay there. Such questions, which are the subject of pharmacokinetics, are usually thoroughly investigated during drug development. Initial studies on pharmacokinetics and also on toxicity are carried out in animals… this document has rather far-reaching implications: it shows that Pfizer—as well as the authorities that were apprised of these data— must have recognized the grave risks of adverse events after vaccination even before the onset of clinical trials. Nevertheless, Pfizer’s own clinical trials failed to monitor any of the clinical risks that were clearly evident from these data, and the regulatory authorities failed to enforce proper standards of oversight. This dual failure has caused the most grievous harm to the public….

What do Pfizer’s animal data presage for biological effects in humans?

  • Rapid appearance of spike protein in the circulation.
  • Toxicity to organs with expected high rates of uptake, in particular placenta and
    lactating breast glands
  • Penetration of some organs might be higher with the real vaccine than with this
    luciferase model…The rapid entry of the model vaccine into the circulation means that we must expect the spike protein to be expressed within the circulation, particularly by endothelial cells. ( Endothelial- The thin layer of cells lining the blood vessels) We have seen before that this will lead to activation of blood clotting through direct activation of platelets and also, probably more importantly, through immune attack on the endothelial cells….

Summary

Pfizer’s animal data clearly presaged the following risks and dangers:

  • blood clotting shortly after vaccination, potentially leading to heart attacks, stroke, and venous thrombosis
  • grave harm to female fertility
  • grave harm to breastfed infants
  • cumulative toxicity after multiple injections

With the exception of female fertility, which can simply not be evaluated within the short period of time for which the vaccines have been in use, all of the above risks have been substantiated since the vaccines have been rolled out—all are manifest in the reports to the various adverse event registries. Those registries also contain a very considerable number of reports on abortions and stillbirths shortly after vaccination, which should have prompted urgent investigation.
….
Of particularly grave concern is the very slow elimination of the toxic cationic lipids. In persons repeatedly injected with mRNA vaccines containing these lipids… this would result in cumulative toxicity. There is a real possibility that cationic lipids will accumulate in the ovaries. The implied grave risk to female fertility demands the most urgent attention of the public and of the health authorities.

Since the so-called clinical trials were carried out with such negligence, the real trials are occurring only now—on a massive scale, and with devastating results. … Calling off this failed experiment is long overdue. Continuing or even mandating the use of this poisonous vaccine, and the apparently imminent issuance of full approval for it are crimes against humanity.” (“The Pfizer mRNA vaccine: pharmacokinetics and toxicity”, The Doctors for Covid Ethics)

Don’t you think people are entitled to know what the government wants to inject into their bodies? Don’t you think they have a right to know how it will effect their immune systems, their vital organs and their overall health? Don’t you think they have the right to decide for themselves which drugs they will take and which they will refuse to take?

Forcing someone to take a drug he does not want, is not just wrong. It’s unAmerican. Which is why people should reject vaccine mandates as a matter of principle. They are an attack on personal liberty, the foundation of our constitutional system. It’s a principle worth dying for.

As for the mass vaccination campaign, it is the most maniacally-genocidal project ever concocted by man. There’s simply no way to calculate the amount of suffering and death we are about to face for trusting people whose policies were obviously shaped by their undiluted hatred of humanity. As German microbiologist Dr. Sucharit Bhakdi said:

“In the end, we’re going to see mass illness and deaths among people who normally would have had wonderful lives ahead of them.”

It is a great tragedy.

“Planned Obsolescence”: The Push for Big Pharma’s Booster Covid Shots and Annual Vaccinations

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By Timothy Alexander Guzman

Source: Silent Crow News

Last month, the CEO from Pfizer, Albert Bourla said that yearly Covid-19 vaccinations may need to become normalized just like the flu shot.   A New York Times article headlined with ‘Booster shots and re-vaccinations could be needed. Drug companies are planning for it’ said that a single shot of the Covid-19 vaccine won’t be enough “Scientists have long said that giving people a single course of a Covid-19 vaccine might not be sufficient in the long term, and that booster shots and even annual vaccinations might prove necessary” but that was just a hypothetical scenario, however “that proposition has begun to sound less hypothetical.”  The article goes on to say that “Vaccine makers are getting a jump-start on possible new rounds of shots, although they sound more certain of the need for boosters than independent scientists have.”  The idea of getting a Covid-19 vaccine shot every year will be difficult task as more people are starting to refuse them because of the lack of trust.  Bourla said that “a third dose of the company’s Covid-19 vaccine was “likely” to be needed within a year of the initial two-dose inoculation — followed by annual vaccinations.”

But there seems to be a problem with these vaccines because people who got vaccinated eventually contracted Covid-19, but the vaccines are supposed to work against the virus, right?  Obviously, all of the vaccines from Pfizer-BioNtech, Moderna, Johnson & Johnson and Astra Zeneca do not work as they claim and because of that, you need to take them annually to protect yourself.  As we know from all of the evidence that has been provided since the launch of these experimental vaccines can cause serious reactions that can lead to a host of injuries and even death in some cases.  In fact, what they are telling you is that they don’t work as well as they expected, but that’s a good thing for them because it creates a population of ‘repeat customers’, sort of like planned obsolescence.  Planned obsolescence according to Wikipedia’s definition is “a policy of planning or designing a product with an artificially limited useful life or a purposely frail design, so that it becomes obsolete after a certain pre-determined period of time upon which it decrementally functions or suddenly ceases to function, or might be perceived as unfashionable.”  Can we apply this definition to the new Covid-19 experimental vaccine market? “The rationale behind this strategy is to generate long-term sales volume by reducing the time between repeat purchases (referred to as “shortening the replacement cycle”). It is the deliberate shortening of a lifespan of a product to force people to purchase functional replacements.”  What is revealing is how this can be described as a business model of Big Pharma’s pursuit of profits:

Planned obsolescence tends to work best when a producer has at least an oligopoly. Before introducing a planned obsolescence, the producer has to know that the customer is at least somewhat likely to buy a replacement from them (see brand loyalty). In these cases of planned obsolescence, there is an information asymmetry between the producer, who knows how long the product was designed to last, and the customer, who does not. When a market becomes more competitive, product life spans tend to increase

So The Flu Shot Must Be Unprofitable

They needed a new product because demand for the flu shot was already in decline due to lack of trust.  An interesting article from August of last year by The National Interest, ‘Flu Shot: Why Do So Many People Refuse to Get Vaccinated?‘ the article is primarily based on doctors who were urging the public to get the annual flu shot. “Despite the touted benefits of getting a flu shot each year, the majority of U.S. adults and about 60% of children still refuse to roll up their sleeves for one, according to the Centers for Disease Control and Prevention’s 2018-2019 data.”  Big Pharma needed a perfect storm to create a new product by first putting the fear in the people and making sure they will go and get their experimental Covid-19 vaccine shot.  The National Interest, a neoconservative foreign policy publication that went on to say that “In the United States, on average, between nine and forty-five million Americans catch the flu each year, which leads to anywhere between 12,000 to 61,000 deaths. Between October 2019 and April 2020, CDC’s data reveal that there were an estimated thirty-nine to fifty-six million influenza infections and 24,000 to 62,000 fatalities” continued “Still, perhaps many don’t see the point of getting vaccinated, especially when the shot’s effectiveness only ranges from 20% to 60% each season—depending on the types of strains circulating.” Then came Covid-19 and the rest is history.

The Covid-19 Experimental Shot is Profitable

According to a website dedicated to the health industry and medical innovations called the Managed Healthcare Executive (MHE) published ‘The Price Tags on the Covid-19 Vaccines’ said that “The race to find both novel and repurposed therapeutics and develop vaccines has been a multinational effort, although heavily funded by U.S. government dollars.” Realistically, government dollars means US taxpayer dollars “but should the vaccine developers profit off their efforts?” You know what the answer will be, but let’s continue “during a House Committee on Energy and Commerce hearing last summer, manufacturers were asked whether they would sell the vaccine at cost.”  Merck did drop out of the vaccine race since no profits were to be made but hey, at least they were honest about their profit motives.  “Moderna and Merck (which announced in January that it was dropping out of the COVID-19 vaccine development race) said they would not sell their vaccines at cost.”  However, Pfizer, BioNTech, AstraZeneca and Johnson & Johnson have received US funding to develop and distribute the experimental Covid-19 vaccines to the public:  

The first vaccine pricing announcement came in July, when the U.S. government contracted with Pfizer and BioNTech to purchase enough vaccines for 50 million Americans. It’s no coincidence that the price of $19.50 per dose was similar to the pricing of the flu shots. Pfizer has said the research and development costs of its the vaccine approach $1 billion, and the company declined to take direct government funding.

But other companies have accepted huge government checks. AstraZeneca received up to $1.2 billion upfront, in exchange for at least 300 million doses. J&J is also receiving government money from the federal government’s Biomedical Advanced Research and Development Authority (BARDA). Early in the pandemic, BARDA agreed to provide $456 million toward the company’s research and development effort. In August, the federal government agreed to pay J&J $1 billion for 100 million doses of its vaccine, thus the $10-a-dose price.

As of mid-July, Boston-based Moderna had received $955 million in U.S. funding. The company said in August that it would charge between $32 and $37 per dose for its vaccine, although company officials also said the price would be adjusted depending on the amount ordered. That may explain the price of $15 per dose price charged to the U.S. for its order of 100 million doses. Still, the company has been criticized for its pricing, partly because it has received so much government research support. The Lown Institute in Boston gave Moderna one of its Shkreli Awards in January. The awards are for the ”worst examples of profiteering and dysfunction in health care”

In terms of profit-making motives plus adding insult to injury, any person who was injured or who had died from any of the experimental vaccines, the manufacturers will not be held liable according to ’42 U.S. Code § 300aa–22 – Standards of responsibility’ which clearly says the following:

No vaccine manufacturer shall be liable in a civil action for damages arising from a vaccine-related injury or death associated with the administration of a vaccine after October 1, 1988, if the injury or death resulted from side effects that were unavoidable even though the vaccine was properly prepared and was accompanied by proper directions and warnings  

At the end of the day, Big Pharma is generating profits and in order to profit from a product, you need repeat customers.  How do you keep your customers?  By continuously spreading fear of an invisible enemy that is always lurking around you and that invisible enemy is Covid-19 and its army of new variants. 

Wake up people! Big Pharma is like every other corporate entity that seeks profits at whatever cost even if it means that people will die from a toxic experimental vaccine that does not protect you against any variant of Covid-19.  These so-called vaccines were produced in under one-year without sufficient human or animal testing, but that’s not important because all they want to do is to keep their corporate board members happy, and that’s all that matters to them at this point. 

A Case of Graphical Correlations: Making Sense of India’s COVID-19 Surge

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By Mathew Maavak

Source: Activist Post

India is currently witnessing a COVID-19 surge of unprecedented proportions, with an allegedly triple-mutant strain stretching the nation’s healthcare infrastructure to the limits.  The uncertainty hanging over the nation is compounded by viral despatches of dead bodies piling up in morgues; of people dropping dead in the streets; of despondent souls jumping off their balconies; and of funeral pyres all over the country. There will be no public service-minded Big Tech censorship in this instance.

This is supposedly Wuhan 2.0. Any social media addict would be forgiven for thinking that India’s population of 1.3 billion might suffer a dip before the year is out.

Amidst the toxic miasma of fear-mongering, coherent explanations over this surge are hard to come by. Therefore, one needs to resort to correlations and proxies in order to gauge causations and effects. For starters, one should compare the yearly death tolls (from all causes) before and after the advent of COVID-19 in India, particularly for the year 2021. But relevant data will only be available a year from now. Many will die as a result of continued lockdowns which generally weaken the immune system. Essential medical procedures will be deferred as hospitals are compelled to focus on COVID-19.  Rising socioeconomic despair will naturally lead to a surge in suicides. In the end, not all coronavirus deaths can be directly attributed to the virus no matter how “experts” add them up.

Other correlations must also be explored in the Indian context. India was rather late in joining the mass vaccination bandwagon. Throughout 2020, its COVID-19 mortality figures were moderate by global standards due to the efficacy of low-cost treatment protocols. Hydroxychloroquine (HCQ) was sanctioned for early stage treatment from March 2020 onwards; while a few months later, India’s most populous state of Uttar Pradesh (population 231 million) replaced HCQ with ivermectin (an anti-parasitic drug).

The results were highly encouraging. As the TrialSiteNews (TSN) reported on Jan 9 2021:

By the end of 2020, Uttar Pradesh — which distributed free ivermectin for home care — had the second-lowest fatality rate in India at 0.26 per 100,000 residents in December. Only the state of Bihar, with 128 million residents, was lower, and it, too, recommends ivermectin.

Despite having the coronavirus situation under control, New Delhi was under immense pressure from various international lobbies and their local proxies to roll out a mass vaccination campaign. It can be argued that India’s ongoing oxygen shortages are the direct result of prioritizing foreign-curated experimental vaccines over local necessities.

While the initial mass vaccination launch was pencilled for Jan 16, the campaign effectively took off only in late February. With uncanny timing, the New York Times hailed India as an “unmatched vaccine manufacturing power” that could counter China in the area of vaccine diplomacy.

As the goal of vaccinating 300 million people by August 2021 neared the midway mark, however, the number of COVID-19 cases surged accordingly. The graph below broadly charts this anomaly.

Not only has India’s COVID-19 cases surged in tandem with increased vaccination, the trajectory of infections and inoculations can be neatly superimposed as the following graph suggests.

Can one infer that there may be a correlation between increased vaccinations and infections? This is not the first time that gene-based therapies ended up creating new viral chimeras. The World Health Organisation (WHO) recently admitted that a Bill & Melinda Gates Foundation (BMGF)-backed vaccine program was responsible for a new polio outbreak in Africa.  The usual suspects were also behind a vaccination-linked polio surge in Pakistan and Afghanistan.

Vaccines causing deadly outbreaks of the very diseases they are supposed to eradicate happen to be a 21st century phenomenon – brought to you by an unholy alliance of Big Tech and Big Pharma. In the process, new mutant strains or “vaccine-derived viruses” emerge, necessitating even more potent vaccines which deliver greater profits and levers of global control to Big Tech. This is how the Davos cabal tries to stay relevant in a century that should otherwise be dominated by Asia. India may end up being the first Asian victim of Big Tech’s Great Reset against the East.

A recent study by Tel Aviv University may shed further light on India’s bizarre surge. It seems those who have been vaccinated with the Pfizer-BioNTech vaccine are 8 times more likely to contract the new South African variant of COVID-19 than the unvaccinated.

The Covishield (Oxford University-AstraZeneca) and Covaxin (Bharat Biotech) vaccines used in India may have produced a similar effect. Dr. Harvey Risch, a professor of epidemiology at Yale University, has estimated that over 60 percent of all new COVID-19 cases seem to occur among the “vaccinated.” Dr Michael Yeadon, former vice president and chief science officer for Pfizer, fears a more alarming outcome which includes the possibility of “massive-scale depopulation”. These are not your average basement-dwelling conspiratorial kooks!

“The vaccine,” to paraphrase Francis Bacon, “is now appearing to be the worse than the disease itself.” Gene-based vaccines open up a Pandora’s Box of what systems theorists call “emergence”. The human body is a complex system that may react unpredictably to interferences at its most substrate (or genetic) levels. As a result, mutant virus strains may emerge alongside unforeseen side effects. This is what we are witnessing worldwide.

But as the virus mutates, so does the official narrative. The Indian Medical Association (IMA) now claims that mass vaccinations in densely-packed stadiums and halls are “superspreader” events. Is the IMA suggesting that new vaccine delivery systems, as lobbied by Big Tech, will solve this problem? Let us wait and see. Furthermore, is close proximity the prime culprit behind the super-surge in India? India is a nation where trains, buses and all forms of public spaces teem with human bodies. Yet, it did not lead to mass casualties in 2020 as many had feared.

In the absence of a watertight scientific explanation from mainstream gatekeepers, a more plausible narrative may be sought from peripheral sources. The Daily Expose offers one such graphic-laden narrative to explain the correlation between mass vaccinations and the rising death toll in India.

While the Daily Expose concedes that correlation does not always equal causation, a similar pattern was noticed in other nations. The vaccination-mortality graph for Mongolia, for example, is particularly eye-popping.

Did Mongolia witness a near-zero to mutant COVID-19 surge just when mass vaccinations rolled out? How coincidental can that be?

The Case of America: Red vs Blue States

One may scientifically argue that India’s surge had nothing to do with ramped-up vaccinations. A new mutant virus may also somehow explain the vaccination-mortality correlations in Mongolia.

Therefore one should resort to another layman-friendly proxy to see whether similar correlations exist elsewhere. How about a comparison within the most coronavirus-affected nation on earth – the United States of America?

Reports thus far suggest that US states which have been resisting mass vaccinations and/or mandatory masking, at least in relative terms, are generally faring better than those adhering to draconian COVID-19 guidelines. Just weeks after Texas lifted its public mask mandate – featuring full crowds at bars, restaurants and concerts  no less – COVID-19 cases as well as hospitalizations dropped to its lowest levels since October 2020. The current White House occupant, who continues to make a buzz over his mental acuity, nonetheless panned the move as a symptom of “Neanderthal thinking”.  In the meantime, South Dakota Governor Kristi Noem, a prominent opponent of mandatory masking, is using COVID-19 restrictions elsewhere to lure businesses to her state. Other red states such as Florida and Arizona have moved to ban the so-called vaccine passports.

Rather coincidentally, the annual flu has virtually disappeared in the United States since the onset of the pandemic. It must be a modern medical miracle!

How will India fare?

With the surge affecting the nation badly, the CEOs of Google, Microsoft and Apple, among others, have pledged heartfelt aid to India. With friends like these, one wonders why Indians cannot question the global COVID-19 narrative on Twitter, Facebook or YouTube without being summarily banned or censored. If India can concede the digital rights of its own citizens and the digital sovereignty of the nation to Big Tech, then how is it going to crowdsource solutions for COVID-19? Or deal with any other future crisis for that matter? An Indian scientific paper which tentatively explored a laboratory origin for COVID-19 can be summarily removed after concerted condemnation from Western academics but a similar claim made by the former head of the US Centers for Disease Control (CDC) appears relatively palatable. Isn’t this a textbook example of neoliberal racism?

Indians should also question why Africa has not been badly affected thus far, despite a South African variant hovering in the region. This is a continent mired in conflicts, poverty, serious healthcare deficits and other Third World-related woes. It lacks world-class scientists and institutions which India admittedly has. Is it because Africa does not pose an economic threat to the Western oligarchy the way Asia does? Or maybe, mass vaccinations haven’t yet taken off in Africa?

For the time being, India cannot reverse course on its vaccination drive and adopt measures similar to the one employed by the Eisenhower administration during the 1957-58 Asian Flu pandemic. The fear genie is already out of the bottle. Big Tech controls the digital narrative in India as it does elsewhere. Even if New Delhi manages to tame the COVID-19 crisis within the next few weeks or months, Big Tech will still be around to stifle India’s destiny.

Ultimately, this game is much bigger than COVID-19; it is about global domination through perennial mass-manufactured crises until a Great Reset is achieved.

Pure, Unalloyed Evil

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By Mike Whitney

Source: The Unz Review

“Hell is empty and all the devils are here.” William Shakespeare, The Tempest

Mike Yeadon is a soft-spoken microbiologist and a former Vice President of Allergy and Respiratory Research at Pfizer. He spent 32 years working for large pharmaceutical companies and is a leading expert on viral respiratory infections. He is also a man on a mission, and his mission is to inform as many people as possible about the elite powerbrokers that are using the pandemic as a smokescreen to conceal their real objectives. Here’s Yeadon in a recent interview:

“If you wanted to depopulate a significant portion of the world, and to do it in a way that wouldn’t require destruction of the environment with nuclear weapons, or poisoning everyone with anthrax or something, And you wanted plausible deniability, whilst you had a multi-year infectious disease crisis; I don’t think you could come up with a better plan of work than what seems to be in from of me. I can’t say that’s what they’re going to do, but I cannot think of a benign explanation for why they are doing it.” (“Interview with Dr Mike Yeadon“, The Delingpole Podcast; Minute 44: 25)

“Depopulation”? Who said anything about depopulation? Isn’t it a bit of a stretch to go from a mass vaccination campaign to allegations of a conspiracy to “depopulate a significant portion of the world”?

Indeed, it is, but Yeadon has done extensive research on the matter and provides compelling evidence that such a diabolical objective may, in fact, be the goal. Moreover, it is not for lack of proof that people are not persuaded that Yeadon is right, but something more fundamental; the inability to grasp that men are capable of almost-unimaginable viciousness and cruelty. Here’s Yeadon again:

“It’s become absolutely clear to me, even when I talk to intelligent people, friends, acquaintances … and they can tell I’m telling them something important, but they get to the point [where I say] ‘your government is lying to you in a way that could lead to your death and that of your children,’ and they can’t begin to engage with it. And I think maybe 10% of them understand what I said, and 90% of those blank their understanding of it because it is too difficult. And my concern is, we are going to lose this, because people will not deal with the possibility that anyone is so evil…

“But I remind you of what happened in Russia in the 20th Century, what happened in 1933 to 1945, what happened in, you know, Southeast Asia in some of the most awful times in the post-war era. And, what happened in China with Mao and so on….

“We’ve only got to look back two or three generations. All around us there are people who are as bad as the people doing this. They’re all around us. So, I say to folks, the only thing that really marks this one out, is its scale.

“But actually, this is probably less bloody, it’s less personal, isn’t it? The people who are steering this … it’s going to be much easier for them. They don’t have to shoot anyone in the face. They don’t have to beat someone to death with a baseball bat, or freeze them, starve them, make them work until they die. All of those things did happen two or three generations back… That’s how close we are.

“And all I’m saying is, some shifts like that are happening again, but now they are using molecular biology.” (“Former Pfizer VP: ‘Your government is lying to you in a way that could lead to your death.“, LifeSite News)

He’s right, isn’t he? Whereas, a great many people know that the government, the media and the public health officials have been lying to them about everything from the efficacy of masks, social distancing and lockdowns, to the life-threatening dangers of experimental vaccines, they still refuse to believe that the people orchestrating this operation, might be pushing them inexorably towards infertility or an early death. They cannot imagine anything so demonic, so they stick their heads in the sand and pretend not to see what is going on right beneath their noses. It’s called “denial” and it is only strengthening the position of the puppetmasters that are operating behind the scenes. Here’s more from Yeadon:

“…In the last year I have realized that my government and its advisers are lying in the faces of the British people about everything to do with this coronavirus. Absolutely everything. It’s a fallacy this idea of asymptomatic transmission and that you don’t have symptoms, but you are a source of a virus. That lockdowns work, that masks have a protective value obviously for you or someone else, and that variants are scary things and we even need to close international borders in case some of these nasty foreign variants get in.” (“Former Pfizer VP: ‘Your government is lying to you in a way that could lead to your death”, Lifesite News)

Many readers may have noticed that this interview appeared on a small Christian website, called “Lifesite News”. Why is that? Shouldn’t the informed observations of a former Pfizer vice president appear on the front pages of the New York Times or Washington Post? Wouldn’t you expect the big cable news channels to run a hot-button interview like this as their headline story?

Of course, not. No one expects that, because everyone knows that the media honchos reflexively quash any story that doesn’t support the “official narrative”, that is, that Covid is the most contagious and lethal virus of all time which requires a new authoritarian political structure and the wholesale evisceration of civil liberties. Isn’t that the underlying storyline of the last year? Covid skeptics and naysayers, like Yeadon, are not allowed to refute the official propaganda or debate the issue on a public forum. They’re effectively banned from the MSM and consigned to the outer reaches of the Internet where only a scattered few will what they have to say. Here’s more:

“Everything I have told you, every single one of those things is demonstrably false. But our entire national policy is based on these all being broadly right, but they are all wrong.”

“But what I would like to do is talk about immune escape because I think that’s probably going to be the end game for this whole event, which I think is probably a conspiracy. Last year I thought it was what I called ‘convergent opportunism,’ that is a bunch of different stakeholder groups have managed to pounce on a world in chaos to push us in a particular direction. So, it looked like it was kind of linked, but I was prepared to say it was just convergence.”

“I [now] think that’s naïve. There is no question in my mind that very significant powerbrokers around the world have either planned to take advantage of the next pandemic or created the pandemic. One of those two things is true because the reason it must be true is that dozens and dozens of governments are all saying the same lies and doing the same inefficacious things that demonstrably cost lives.

“And they are talking the same sort of future script which is, ‘We don’t want you to move around because of these pesky… “variants”… they are all saying ‘don’t worry, there will be “top-up” vaccines that will cope with the potential escapees.’ They’re all saying this when it is obviously nonsense.” (“Former Pfizer VP: ‘Your government is lying to you in a way that could lead to your death”, Lifesite News)

Let’s pause for a minute, and ask ourselves why a modest, self-effacing microbiologist who operated in the shadows for his entire professional career, has thrust himself into the limelight when he knows, for certain, he will either be ridiculed, smeared, discredited, dragged through the mud or killed. In fact, he openly admits that he fears for his safety and assumes that he could be “removed” (‘assassinated’) by his enemies. So, why is he doing this? Why is he risking life and limb to get the word out about vaccines?

It’s because he feels a moral obligation to warn people about the danger they face. Yeadon is not an attention-seeking narcissist, in fact, he’d rather vanish from public-life altogether. But he’s not going to do that because he’s selflessly committed to doing his duty by sounding the alarm about a malign strategy that may well lead to the suffering and death of literally tens of millions of people. That’s why he’s doing it, because he’s an honorable man with a strong sense of decency. Remember decency?. . Here’s more:

“You can see that I am desperately trying not to say that it is a conspiracy, because I have no direct evidence that it is a conspiracy. Personally, all my instincts are shouting that it’s a conspiracy as a human being, but as a scientist, I can’t point to the smoking gun that says they made this up on purpose.” (“Yeadon Interview, Delingpod, minute 41:25)

Many of us who have followed events closely for the last year and have searched the internet for alternate points of view, are equally convinced that it is a conspiracy, just as Russiagate was a conspiracy. And while we might not have conclusive, rock-solid proof of criminal activity, there is voluminous circumstantial evidence to support the claim. By definition, a “conspiracy” is “an evil, unlawful, treacherous, or surreptitious plan formulated in secret by two or more persons.” (Dictionary.com) What is taking place presently across the western world, meets that basic definition. Just as the contents of this article meets the basic definition of a “Conspiracy theory“, which is: “an attempt to explain harmful or tragic events as the result of the actions of a small powerful group. Such explanations reject the accepted narrative surrounding those events; indeed, the official version may be seen as further proof of the conspiracy.” (Britannica)

We make no attempt to deny that this is a conspiracy theory, any more than we deny that senior-level officials at the FBI, CIA, DOJ and US State Department were involved in a covert operation aimed at convincing the American people that Donald Trump was a Russian agent. That was a conspiracy theory that was later proven to be a fact. We expect that the facts about the Covid operation will eventually emerge acquitting us on that account as well. Here’s more from Yeadon:

“I think the end game is going to be, ‘everyone receives a vaccine’… Everyone on the planet is going to find themselves persuaded, cajoled, not quite mandated, hemmed-in to take a jab.

“When they do that every single individual on the planet will have a name, or unique digital ID and a health status flag which will be ‘vaccinated,’ or not … and whoever possesses that, sort of single database, operable centrally, applicable everywhere to control, to provide as it were, a privilege, you can either cross this particular threshold or conduct this particular transaction or not depending on [what] the controllers of that one human population database decide. And I think that’s what this is all about because once you’ve got that, we become playthings and the world can be as the controllers of that database want it.” (LifeSite)

So mass vaccination is actually the pathway to absolute social control by a technocratic elites accountable to no one? Are we there yet?

Pretty close, I’d say. Here’s more:

“And they are talking the same sort of future script which is, ‘We don’t want you to move around because of these pesky “variants”’— (but) ‘don’t worry, there will be “top-up” vaccines that will cope with the potential escapees.’ They’re all saying this when it is obviously nonsense.”

Is he right? Is the variant hobgoblin now being invoked to prolong the restrictions, intensify the paranoia and pave the way for endless rounds of mass vaccination?

Judge for yourself, but here’s a sampling of articles that appeared in today’s news that will help you decide:

1– Reuters, South African variant can ‘break through’ Pfizer vaccine, Israeli study says

“The coronavirus variant discovered in South Africa can “break through” Pfizer/BioNTech’s COVID-19 vaccine to some extent, a real-world data study in Israel found, though its prevalence in the country is low and the research has not been peer reviewed….

“We found a disproportionately higher rate of the South African variant among people vaccinated with a second dose, compared to the unvaccinated group. This means that the South African variant is able, to some extent, to break through the vaccine’s protection,” said Tel Aviv University’s Adi Stern. (So, according to the article– the vaccine doesn’t work.)

2– The New York Times: Rise of Variants in Europe Shows How Dangerous the Virus Can Be

“Europe, the epicenter of the coronavirus pandemic last spring, has once again swelled with new cases, which are inundating some local hospitals and driving a worrisome global surge of Covid-19.

But this time, the threat is different: The rise in new cases is being propelled by a coronavirus variant first seen in Britain and known as B.1.1.7. The variant is not only more contagious than last year’s virus, but also deadlier.

The variant is now spreading in at least 114 countries. Nowhere, though, are its devastating effects as visible as in Europe, where thousands are dying each day and countries’ already-battered economies are once again being hit by new restrictions on daily life….

Vaccines will eventually defeat the variants, scientists say. (So, they don’t work now??) And stringent restrictions can drive down cases of B.1.1.7. (So, don’t leave your home.)..

“We’ve seen in so many countries how quickly it can become dominant,” said Lone Simonsen, a professor and director of the PandemiX Center at Roskilde University in Denmark. “And when it dominates, it takes so much more effort to maintain epidemic control than was needed with the old variant.” (In other words, we are effectively dealing with a different pathogen that requires a different antidote. It’s an admission that the current crop of vaccines doesn’t work.)

3– SARS-CoV-2 variants B.1.351 and P.1escape from neutralizing antibodies, cell.com

“….our findings indicate that the B.1.351and P.1 variants might be able to spread in convalescent patients or BNT162b2-vaccinated individuals and thus constitute an elevated threat to human health. Containment of these variants by non-pharmaceutic interventions is an important task.” (Note– In other words, the new vaccines don’t work against the new Covid strains, so we might need to preserve the onerous lockdown restrictions forever.)

How can people read this fearmongering bunkum and not see that it is designed to terrify and manipulate the masses into sheeplike compliance?

There’s no denying that the variant is being used to fuel the Covid hysteria and perpetuate the repressive social restrictions. So, the question we should be asking ourselves is whether we can trust what we are being told by the media and the public health officials?

And the answer is “No”, we cannot trust them. They have repeatedly misled the public on all manner of topics including masks, asymptomatic transmission, immunity, Infection Fatality Rate, social distancing and now variants. According to Sunetra Gupta, who is Professor of Theoretical Epidemiology in the Department of Zoology at the University of Oxford, and a Royal Society Wolfson Research Fellow:

“...some of these variants could be more transmissible, but the truth is… even with a marginal increase in transmissibility… that does not have much of a material effect or difference in how we deal with the virus. In other words, the surge of the virus cannot be ascribed to a new variant….

The other question is are these variants more virulent, and the truth is we don’t know, but it is unlikely because the data don’t seem to say so despite the scary headlines…Pathogens tend to evolve towards lower virulence….because that maximizes their transmissibility…It is much more probable that these strains will not be materially so different that we would have to alter our policies.” (Sunetra Gupta: Are these new variants more transmissible?” You Tube)

So, according to Gupta, even if the new strains of Covid are more transmissible, it is highly-unlikely that they are more lethal.

Here’s more on the topic from Diagnostic pathologist, Dr Claire Craig who provides a more technical explanation:

“SARS-CoV-2 genetic sequence has ~30,000 letters. Alterations in a handful of letters will not change it’s shape much – if it did it wouldn’t function properly anyway. Fear mongering about immune escape is not needed and is irresponsible especially when no evidence to support the claims.” (Claire Craig)

In essence, Craig is saying the same thing we said earlier, that the slight mutations to the infection will not impact the immune reaction of people who already had the virus. Thus, the current crop of “variants” should not be a cause for alarm. If you have already had Covid or if you already have prior-immunity due to previous exposure to similar infections, (SARS, for example) the new strain should not be a problem. It should also not be a problem if the new vaccines provide the type of broad-based immunity that one should expect of them. Again, the mutations represent only the slightest change in the composition of the pathogen (less than 1%), which means that –if the vaccines don’t work– they are, in effect, useless.

Here’s a longer explanation that some readers might find overly technical and perhaps tedious, but it’s worth wading through in order to see that the media is deliberately misstating the science to terrify the public. This excerpt is from an article by Yeadon. Here’s what he said:

“The idea is planted in people’s mind that this virus is mutating in such a way as to evade prior immunity. This is completely unfounded, certainly as regards immunity..(that is) gained naturally, after repelling the virus ….

It’s important to appreciate that upon infection, the human immune system cuts up an infectious agent into short pieces. Each of these short pieces of protein are presented to other cells in the immune system, like an identity parade. …These have a range of functions. Some make antibodies & others are programmed to kill cells infected by the virus, recognized by displaying on their surface signals that tell the body that they’ve been invaded.

In almost all cases,… this smart adaptive system overcomes the infection. Crucially… this event leaves you with many different kinds of long-lived ‘memory’ cells which, if you’re infected again, rapidly wipe out any attempt at reinfection. So, you won’t again be made ill by the same virus, and because the virus is simply not permitted to replicate, you are also no longer able to participate in transmission….

The general ‘direction of travel’ (for viruses) is to become less injurious but easier to transmit, eventually joining the other 40 or so viruses which cause what we collectively term ‘the common cold”.

What generally doesn’t happen is for mutants to become more lethal to the hosts (us). But the key point I wanted to get across is just how large SARS-COV-2 is. I recall it’s of the order of 30,000 letters of genetic code which, when translated, make around 10,000 amino acids in several viral proteins. Now you can see that the kinds of numbers of changes in the letters of the genetic code are truly tiny in comparison with the whole. 30 letter changes might be roughly 0.1% of the virus’s code. In other words, 99.9% of that code is not different from the so-called Wuhan strain. Similarly, the changes in the protein translated from those letter code alterations are overwhelmed by the vast majority of the unchanged protein sequences. So your immune system, recognizing as it does perhaps dozens of short pieces…. will not be fooled by a couple of small changes to a tiny fraction of these. No: your immune system knows immediately that this is an invader it’s seen before, and has no difficulty whatsoever in dealing with it swiftly & without symptoms. So, it’s a scientifically invalid…

… even if mutations did change a couple of these, the majority of the pieces…. of the mutated virus will still be unchanged & recognized by the vaccine-immune system or the virus-infected immune system & a prompt, vigorous response will still protect you.” (“Variants, Covid”, Michael Yeadon, My Thread Reader)

Let’s summarize:

We have presented the informed views of three reputable scientists all of who explicitly refute the idea that the so called “variants”:

  1. Are more lethal
  2. Have the potential to reinfect people who have already had Covid
  3. Have mutated enough to reinfect people who have already been vaccinated (unless, of course) the vaccine does not provide broad-based immunity to begin with. (which is possible since Phase 3 long-term trials were never conducted.)

So, why are the public health officials and the media lying about this matter which is fairly clear-cut and uncontroversial? That is the question.

Yeadon concludes that there is something flagrantly diabolical about their denial. He thinks they are lying in order to dupe more people into getting injected with a substance that will either render them infertile, cause them great bodily harm or kill them outright. Take your pick. Here’s more:

“The eugenicists have got hold of the levers of power and this is a really artful way of getting you to line-up and receive some unspecified thing that will damage you. I have no idea what it will actually be, but it won’t be a vaccine because you don’t need one. And it won’t kill you on the end of the needle because you would spot that.

“It could be something that will produce normal pathology, it will be at various times between vaccination and the event, it will be plausibly deniable because there will be something else going on in the world at that time, in the context of which your demise, or that of your children will look normal.

“That’s what I would do if I wanted to get rid of 90 or 95% of the world’s population. And I think that’s what they’re doing.” (LifeSite)

“The eugenicists have got hold of the levers of power”?

Has Yeadon gone mad? Has the pressure of the global pandemic pushed him off the deep end or is he ‘on to something’ big, something that no one even dares to even think about; a plan so dark and sinister that its implementation would constitute the most grievous and coldblooded crime against humanity of all time; the injection of billions of people with a toxic elixir whose spike protein dramatically compromises their immune systems clearing the way for agonizing widespread suffering followed by mountains of carnage?

There are others, however, who see a connection between the current vaccination campaign and “the eugenicists”, in fact, Dr. Joseph Mercola points to the link between the lead developer of the AstraZeneca vaccine, Adrian Hill, and the Eugenics movement. According to Mercola:

“Hill gave a lecture at the Galton Institute (which was known as the U.K. Eugenics Society) in 2008 for its 100-year anniversary. As noted in Webb’s article:8

“Arguably most troubling of all is the direct link of the vaccine’s lead developers to the Wellcome Trust and, in the case of Adrian Hill, the Galton Institute, two groups with longstanding ties to the UK eugenics movement.

The latter organization, named for the ‘father of eugenics’ Francis Galton, is the renamed U.K. Eugenics Society, a group notorious for over a century for its promotion of racist pseudoscience and efforts to ‘improve racial stock’ by reducing the population of those deemed inferior.

The ties of Adrian Hill to the Galton Institute should raise obvious concerns given the push to make the Oxford-AstraZeneca vaccine he developed with [Sarah] Gilbert the vaccine of choice for the developing world, particularly countries in Latin America, South and Southeast Asia, and Africa, the very areas where the Galton Institute’s past members have called for reducing population growth …

Emeritus professor of molecular genetics at the Galton Institute and one of its officers is none other than David J. Galton, whose work includes ‘Eugenics: The Future of Human Life in the 21st Century.’

David Galton has written that the Human Genome Mapping Project… had ‘enormously increased … the scope for eugenics … because of the development of a very powerful technology for the manipulation of DNA.’

This new ‘wider definition of eugenics,’ Galton has said, ‘would cover methods of regulating population numbers as well as improving genome quality by selective artificial insemination by donor, gene therapy or gene manipulation of germ-line cells.’ In expanding on this new definition, Galton is neutral as to ‘whether some methods should be made compulsory by the state, or left entirely to the personal choice of the individual….

“The Wellcome Centre regularly cofunds the research and development of vaccines and birth control methods with …. a foundation (name withheld) that actively and admittedly engages in population and reproductive control in Africa and South Asia by, among other things, prioritizing the widespread distribution of injectable long-acting reversible contraceptives (LARCs).

The Wellcome Trust has also directly funded studies that sought to develop methods to ‘improve uptake’ of LARCs in places such as rural Rwanda….’ LARCs afford women in the Global South ‘the least choice possible short of actual sterilization.’

Some LARCs can render women infertile for as long as five years, and, as Levich argues, they ‘leave far more control in the hands of providers, and less in the hands of women, than condoms, oral contraceptives, or traditional methods.’…

Slightly modified and rebranded as Jadelle, the dangerous drug was promoted in Africa… Formerly named the Sterilization League for Human Betterment, EngenderHealth’s original mission, inspired by racial eugenics, was to ‘improve the biological stock of the human race.’” (“Exploring the Oxford-AstraZeneca Eugenics Links”, Mercola.com)

So, how does “eugenics” factor into the creation and distribution of the mRNA vaccine? Is there a link or are we grasping at straws?

We can’t answer that question, but a recent article by Mathew Ehret at The Off-Guardian provides a few interesting clues. Here’s what he said:

“The fact that the organizations promoting the rise of this eugenics policy throughout Nazi Germany and North America included such powerhouses as the Rockefeller Foundation, the Wellcome Trust and the Human Sterilization League for Human Betterment… which have all taken leading roles in the World Health Organization over recent decades is more than a little concerning.

The fact that these eugenics organizations simply re-branded themselves after WWII and are now implicated in modern RNA vaccine development alongside the Galton Institute (formerly British Eugenics Association), Oxford’s AstraZeneca, Pfizer and the…. Foundation should give any serious thinker pause as we consider what patterns of history we are willing to tolerate repeating in our presently precarious age.” (“Nazi Healthcare Revived Across the Five Eyes: Killing Useless Eaters and Biden’s COVID Relief Bill”, The Off-Guardian)

We’ll end this piece with an excerpt from a 2010 article by Andrew Gavin Marshall at Global Research who presciently noted that:

“Eugenics is about the social organization and control of humanity…. (particularly) population control….

The ideas of Malthus, and later Herbert Spencer and Charles Darwin were remolded into branding an elite ideology of “Social Darwinism”, which was “the notion that in the struggle to survive in a harsh world, many humans were not only less worthy, many were actually destined to wither away as a rite of progress. To preserve the weak and the needy was, in essence, an unnatural act.” This theory simply justified the immense wealth, power and domination of a small elite over the rest of humanity, as that elite saw themselves as the only truly intelligent beings worthy of holding such power and privilege.

Francis Galton later coined the term “eugenics” to describe this emerging field. His followers believed that the ‘genetically unfit’ “would have to be wiped away,” using tactics such as, “segregation, deportation, castration, marriage prohibition, compulsory sterilization, passive euthanasia – and ultimately extermination.”… Sir Julian Huxley was also a life trustee of the British Eugenics Society from 1925, and its President from 1959-62. … “Huxley believed that eugenics would one day be seen as the way forward for the human race,” and that, “A catastrophic event may be needed for evolution to move at an accelerated pace.”…. It is much the same with ideas whose time has not yet come; they must survive periods when they are not generally welcome.”

The 21st-century technologies are so powerful that they can spawn whole new classes of accidents and abuses. Most dangerously, for the first time, these accidents and abuses are widely within the reach of individuals or small groups. They will not require large facilities or rare raw materials. Knowledge alone will enable the use of them…. I think it is no exaggeration to say we are on the cusp of the further perfection of extreme evil, an evil whose possibility spreads well beyond that which weapons of mass destruction bequeathed to the nation-states, on to a surprising and terrible empowerment of extreme individuals.

…. Due to improved techniques the elite will have greater control over the masses; and because human work will no longer be necessary the masses will be superfluous, a useless burden on the system. If the elite is ruthless they may simply decide to exterminate the mass of humanity. If they are humane they may use propaganda or other psychological or biological techniques to reduce the birth rate until the mass of humanity becomes extinct, leaving the world to the elite….

A horrifying vision indeed; but one which builds upon the ideas of Huxley, Russell and Brzezinski, who envisioned a people who – through biological and psychological means – are made to love their own servitude. Huxley saw the emergence of a world in which humanity, still a wild animal, is domesticated; where only the elite remain wild and have freedom to make decisions, while the masses are domesticated like pets. Huxley opined that, “Men and women will grow up to love their servitude and will never dream of revolution. There seems to be no good reason why a thoroughly scientific dictatorship should ever be overthrown.” (“New Eugenics and the Rise of the Global Scientific Dictatorship”, Andrew Gavin Marshall, Global Research)

We must ask ourselves whether the current mass vaccination campaign is a science-based effort to relieve sickness and disease or a fasttrack to a dark and frightening dystopia conjured up by evil men seeking to tighten their grip on all humanity?

Pfizer’s Experimental Covid-19 Vaccine—What You’re Not Being Told

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Pfizer’s long history of scandals, and the fact that they have never been held to account for their crimes, continues to be ignored by the media, even as its experimental mRNA vaccine candidate for Covid-19 draws ever closer to US government approval.

By Johnny Vedmore

Source: Unlimited Hangout

The vaccine information war has kicked up a gear, and the mainstream media vultures are circling to descend on any content that they can easily label and dismiss as misinformation. Laws will be passed throughout legislatures globally to criminalise anyone who publicly misunderstands any part of the complex biological processes involved in many of the new experimental vaccine technologies that are being used to produce Covid-19 vaccine candidates.

Even now, intelligence agencies and intelligence-backed tech companies are set to deploy sophisticated methods to censor content and deplatform news websites that they view as promoting ‘vaccine hesitancy’ as well as ‘vaccine misinformation’, particularly as a Covid-19 vaccine candidate lurches closer to approval.

It is expected that by month’s end the mRNA vaccine produced by the scandal-ridden pharmaceutical giant Pfizer will be approved by the US government via an emergency-use authorization, with other countries expected to follow suit. Pfizer, in anticipation of the seemingly imminent and assured approval of their vaccine candidate, has already been manufacturing hundreds of millions of doses of its vaccine for weeks and has received praise from governments and mainstream media alike for its self-reported claims that its vaccine is 90 percent effective.

In particular, the success of the experimental mRNA mass vaccination program appears to hinge on the general population being unable to effectively articulate their concerns and objections. Whilst the mainstream media are quick to point out when somebody makes an error in how they believe the mRNA vaccine works, they don’t offer any further information than the official government line. Public distrust in vaccination programs is not the fault of those who don’t understand the way this brand-new technology works. Public distrust is all-pervasive because only one side of the argument is allowed to be heard. We do need to understand the technology involved, as there is a difference between mRNA vaccines and DNA vaccines. Having a general understanding of the reason why someone should object to being given an experimental mRNA vaccine is necessary for creating a clear and coherent argument.

We are about to examine a subject that has been one of the most censored topics in the modern era. But now, more than ever before, we are in desperate need of the information that is being systematically hidden from the public. This article will be banned and attacked by those who believe we, the general public, shouldn’t know all the information about what they want to achieve from the coming mass global vaccinations. The reason for the current establishment’s unwillingness to speak about this subject leads to perhaps unnecessary suspicion. Such suspicions will never be dismissed via the currently employed tactic of smearing anyone who questions intentions. If governments worldwide want their populations to submit to these vaccinations, then they need to stop patronising people and speak honestly. However, since that is unheard of, they will continue to employ coercive tactics, as they will be trying out a never-before-approved experimental method to boost the immune system by manipulating the process our DNA uses to signal for the creation of certain proteins, and we have little idea of what the long-term impact this brand-new therapeutic technology could have on our health. No politician, medical expert, or pharmaceutical representative is willing to accept responsibility for challenges that might be around the corner.

Many of the pharmaceutical companies researching potential coronavirus vaccines are using old methods. They take a proverbial pinch of the virus and infect your immune system at a very low and slow rate, allowing your body the time it needs to build up a natural immunological resistance to the illness. But developing those types of vaccines is a slow and arduous process, and the current leaders in the race to mass global vaccination are pharmaceutical companies using a radical new method that has never been tried before.

‘They are going to hack the cells in your body in order to make them into drug factories’, says Nathan Vardi, a staff writer for Forbes, in a video titled Why Pfizer Is Betting Big on an Unproven Treatment for Covid-19, from March 2020. ‘The problem is with this approach’, Vardi admits, ‘is there’s never been an approved mRNA product’.

The various scientific explorations into the therapeutic applications of potential mRNA treatments are still in their infancy, but the method has been lauded as a potential solution to the treatment of cancer and infectious diseases, for protein replacement, and for gene therapy.

In January 2020, the de facto leader in the mRNA field was the pharmaceutical company Moderna, but—in the wake of Covid-19—other major companies began to focus on the mRNA method. Moderna was able to pioneer that method several years ago, thanks to funding largely provided by the Pentagon’s Defense Advanced Research Projects Agency (DARPA) and the Bill and Melinda Gates Foundation.

Now, as 2020 draws to a close, the race to develop the winning Covid-19 vaccine is in full swing, and another Big Pharma company has seemingly beaten Moderna to the development of a supposedly effective mRNA vaccine, thanks to Pfizer teaming up with BioNTech, a small German company, to pip Moderna to the post. But, in this race to ‘save humanity’, there are bound to be pitfalls, especially when introducing completely new health technologies into mainstream use. Has Pfizer rung the finishing bell in this global race to end the current pandemic, or, instead, is it hurtling towards a disaster of epic proportions?

There are very informative scientific papers available from just before the pandemic began that give us an insight into this new mRNA technology. So here I’ll examine the DNA manipulating method, the vaccine, the people behind the research and development at BioNTech, but most important, I’ll examine Pfizer, and look at how the company has avoided accountability when things go wrong—and things do go wrong at Pfizer.

mRNA Vaccine Technology and How It Works

The vital interaction that mRNA has with our DNA has made selling mRNA vaccine technology extremely difficult for those who believe it’s the future of human medicine. The fact that it will alter the function of your DNA in your body has made many people suspicious of what unexpected horrors could arise through mass use of this new and experimental technique.

Unsurprisingly, the people marketing the vaccines have tried to downplay the aggressive and genetically manipulative nature of the treatment. In fairness, trying to explain the workings of such a complex new technology in plain English is exceedingly difficult. This is apparent when one listens to representatives of the mainstream media, who are often mealy mouthed when describing the biological processes that will take place when you receive the mRNA vaccine. But inability to articulate the technology isn’t surprising when you consider that part of your DNA, after breaking in two through a natural process, will then be combined with the experimental mRNA in a way that seems esoteric to many of us. It’s almost impossible to imagine such a process taking place in one’s own vulnerable biological system, in one’s DNA, the most precious building blocks of life that define your very existence.

After a preprogrammed strand of mRNA has merged with a naturally severed part of your DNA, it will request the production of a protein that should help trigger your immune system. In theory, this should boost your immune system and aid in the mass production of the proteins necessary to successfully fight the specific illness. The inserted messenger-RNA (thus, mRNA) should be relatively easy to design and programme as long as the scientists involved have the genetic coding for the infection it is to fight. In this case, the necessary data was released in January 2020 by the Chinese. Mild side effects to this process should be expected.

Although no extreme side effects were reported by Pfizer during the stage 3 testing of their mRNA vaccine, nearly every participant suffered mild symptoms, including swelling of the arm, irritation of the skin, and headaches, to name just a few. But, as we shall see, the information that Pfizer releases about its clinical trials and what happens in reality can be quite different.

I have just described the basic information you require for understanding how the coming mRNA vaccine works, but what I can’t describe to you is what happens in the long term. This form of therapeutic alternative has never been allowed or sanctioned before, aside from small clinical trials. There has never been an FDA-approved clinical trial for mRNA medicine because its usage comes with an abundance of ethical and moral questions and unknown possibilities.

At the same time, the utilisation of the mRNA method could also be one of the biggest leaps forward in technology ever recorded in human history. If we give the technology the benefit of the doubt and assume that it has no negative long-term side effects, then it is a potential treatment for almost every human illness on earth. Opening this mRNA floodgate would mean normalising regular vaccinations for nearly every imaginable ailment. In the best-case scenario, you could be vaccinated against cancer, heart disease, diabetes, dementia and Alzheimer’s, and any other human ailment that derives from a fault in your DNA. In the worst-case scenario, you could be left dead or crippled like Pfizer’s victims in its experiments on Nigerian children during the late 1990s.

All that being said, the Pfizer/BioNTech vaccine has a major downside to it. Pfizer and Moderna have stated that their mRNA vaccines need to be kept at -70° C and -20° C, respectively, which is a significant logistical challenge. Without these extremely cold temperatures, the mRNA and combined nanoparticles will lose their integrity. There are no studies on the effect of poorly stored mRNA vaccines on the human body. In comparison, DNA vaccines are much easier to transport and store as they are much more stable molecules.

As we have seen, the potential for mRNA technology is boundless. If the vaccine is successful in normalising the process of gene editing for medicinal benefit, there will be pressure to continue editing genes in other ways. It isn’t hard to see that the technology could have cosmetic, medical, and military applications that could range from phosphorescent skin to military bioweapons beyond our imagination. That is the reason why the people behind this technology are reluctant to speak about its potential game-changing mRNA method, for it represents our first real steps into transhumanism.

Pfizer’s Profitable Partnership with Germany’s BioNTech

As we have seen, Pfizer wasn’t the primary company in the mRNA business at the turn of 2020, but its immediate partnership with BioNTech saw it beat its main competitor, Moderna, to the finish line. BioNTech, based in Mainz, Germany, is led by a husband and wife team and, prior to the partnership with Pfizer, was dedicated to mRNA-related cancer-treatment research.

Uğur Şahin and Özlem Türeci, the couple leading BioNTech, are of Turkish descent. Şahin’s family were from southern Turkey, and he studied for his doctorate in Cologne, whilst Türeci’s family came from Istanbul. The two met at the University of Hamburg.

BioNTech already had a collaboration agreement to develop mRNA‐based vaccines for prevention of influenza with Pfizer as far back as February 2019, and their commercial strategy of collaborating with selected partners paid off when the race to the coronavirus vaccine began. Since then, there has been global media interest in BioNTech, mainly in the form of puff pieces focussing on Şahin and Türeci’s romantic life. But BioNTech also has many links to other Big Pharma giants and some of the well-known movers and shakers in the medical world. As well as its partnership with Pfizer, in 2019 BioNTech also had partnership deals with Bayer, Genentech, Sanofi, Genmab, Eli Lilly, Roche, and of course they received funding from the Bill and Melinda Gates Foundation. In September 2019, just before the first people were infected with the new strain of SARS-CoV-2, the German news outlet Handelsblatt reported that ‘the Gates Foundation is investing around 50 million euros in the Mainz biotech company BioNTech. The money will be used to research HIV and tuberculosis vaccines’.

BioNTech has a small five-person management team and a four-person supervisory board. Şahin is the CEO of the company; he was also the head of the scientific advisory board of Ganymed Pharmaceuticals AG from 2008 until 2016, when the company was acquired by Astellas Pharma. BioNTech’s chief business officer, Sean Marett, previously worked in global strategic and regional marketing, and in sales at GlaxoSmithKline in the United States and at Pfizer Europe, as well as for Evotec and Lorantis. The company’s chief operating officer and CFO, Dr Sierk Poetting, joined BioNTech in September 2014 from Novartis. The chief strategy officer at BioNTech is Ryan Richardson, who had previously been an executive director of the global health-care investment-banking team at J. P. Morgan in London, where he advised companies in the biotech and life sciences industry on mergers and acquisitions, equity, and debt capital finances. The German BioNTech’s four-man supervisory board includes Ulrich Wandschneider, who is also a member of Trilantic Europe.

Pfizer: A Company Never Held to Account

If it were only BioNTech that was responsible for the creation of this futuristic vaccine technology, then maybe people would have more faith in the product. But Pfizer casts a dark shadow of conspiracy wherever it does business. Pfizer’s previous use of experimental drugs in secretive and scandalous studies has inspired Hollywood movies and court cases lasting over a decade, as it resulted in the death of many children. Yet, the media organisations touting its coronavirus vaccine as a heaven-sent miracle have provided little to no coverage of Pfizer’s previous experimental disasters.

Pfizer entered into the vaccine business in late 2006 by acquiring the British influenza-vaccine company PowderMed for an undisclosed fee. Pfizer was admittedly excited about the deal, stating that ‘PowderMed’s unique DNA vaccine technology is particularly promising’ and that ‘its pipeline of vaccine candidates for influenza and chronic viral diseases could have major potential’. In fact, beginning in autumn 2005, many Big Pharma companies had taken their first steps into the vaccine industry. Novartis entered the vaccine business by acquiring 56 percent of Chiron, whilst GlaxoSmithKline expanded its vaccine base by acquiring ID Biomedical of Canada. Competition was heating up among the big players, and the vaccine industry was seen as a safe bet, with reports of new vaccines selling for hundreds of dollars. But Pfizer’s reputation over the preceding decade had taken a severe knock due to the company’s disastrous experimental trials in Africa.

In 1996, an experimental trial took place in Nigeria. Under the cover of severe outbreaks of cholera, measles, and meningitis in northern Nigeria, Pfizer set up the secretive trials in Kano, the second largest city in Nigeria, to test its experimental antibiotic, Trovan (trovafloxacin). It tested the experimental drug on two hundred children. The children’s parents assumed that the children would receive the standard meningitis jab, but Pfizer staff instead set up two control groups. Half of the children were given the experimental Trovan, and the other hundred were given a reduced dosage of the leading meningitis equivalent. The lower dose was to help artificially skew the results in the favour of Trovan for marketing and competitive purposes.

In 2002, a group of Nigerian children and their legal guardians sued Pfizer in the US District Court for the Southern District of New York. In court documents, the plaintiffs alleged that five children who received Trovan and six children whom Pfizer had ‘low-dosed’ had died as a result, whilst others suffered paralysis, deafness and blindness. The alleged actual number of those who died due to their involvement in the trial, per Nigerian sources, is over fifty.

Pfizer was supposed to check the children’s blood samples five days into the trials to look for any abnormalities and then change their treatment to the full-strength leading meningitis drug if there were any problems. However, they failed to do so. Instead, the Pfizer team waited for the irreversible symptoms to manifest physically before switching the treatment for the study’s unwitting participants. After realising that they had just murdered and crippled these children, Pfizer, like any giant pharmaceutical corporation would, left the scene of the crime in a hurry, failing to do any further evaluation of the patients.

Pfizer spent the next ten years denying any responsibility for the disaster, eventually releasing a statement entitled ‘Trovan, Kano State Civil Case—Statement of Defense’, in which the pharmaceutical bigwig stated among other things ‘that mortality in the patients treated by Pfizer was lower than that observed historically in African meningitis epidemics, and that no unusual side effects, unrelated to meningitis, were observed after 4 weeks’.

Pfizer eventually settled the case for $75 million on condition that it would not be held responsible for its actions. The Guardian newspaper reported in 2011 that the first four settlements in the lengthy court battle had been given to the families of four of the children who were killed during the trial. In an unabashed attempt to make the court settlement of $175,000 harder for each of the surviving families to claim, the victims’ families were forced to provide DNA samples to prove they were actually related to the deceased. This tactic turned out to be very effective from the company’s perspective, as many of the families didn’t trust Pfizer, which led some to pull out and refuse the settlement because they thought the DNA samples were a ploy by Pfizer to commit further illegal secret experiments upon them, or worse.

The Nigerians were represented by two brave lawyers, a Nigerian lawyer named Etigwe Uwo and a Connecticut-based lawyer, Richard Altschuler. According to Altschuler, it was the story of Pfizer’s Kano coverup that prompted John le Carré to write the novel The Constant Gardener that was adapted in the feature film. Like the situation depicted in the movie, Pfizer used scare tactics and smear campaigns to try and hinder any investigation into the Kano incident.

In 2006, Pfizer cut its workforce by 20 percent, reducing the number of its US employees by 2,200 people. The Financial Times reported on 29 November 2020 that this was something that was happening in all of the major pharmaceutical firms stating, ‘Big pharma is rushing to restructure across its business from manufacturing to how it markets and sells its drugs’. But Pfizer was mainly concentrating on radical change to its drugs salesforce.

Pfizer was hit by further major scandals over the following year. One included the illegal premarketing of the HIV drug Maraviroc, which initially stalled the drug’s approval by the FDA. The scandal saw Pfizer publicly fire three of its top executives, including its assistant sales manager, Kelly Fitzgerald, (who returned to work for Pfizer and is currently their assistant sales director), HIV sales director, Art Rodriguez, now working for California’s Valued Trust, and the Mid-Atlantic director, Bob Mumford.

Get Your Facts Straight and Another Way Out

Whilst a DNA vaccine will change your DNA permanently, an mRNA vaccine will not permanently change your DNA. It takes one sentence to clear up that misunderstanding of the technology, and people should not be criminalised for such a simple misunderstanding. However, the mRNA vaccine does bind with part of your DNA to alter the proteins being produced. This is the very place where companies wish to trap opponents of their experimental vaccine campaigns. Just because someone doesn’t fully understand the process involved shouldn’t mean they should be demonised and forced into taking this experimental combination of nanoparticles. In fact, individuals should reject the vaccine until companies explain how it works and if there are any long-term side effects. You shouldn’t let anybody put anything into your body until they can tell you if any long-term consequences could occur. This is a basic principle of self-preservation that trumps any risk of a virus, especially a virus that has proven to be just a little bit more deadly than the common flu.

Our bodies should be the most important concern for us all. Fundamentally speaking, all our liberties and freedoms are of little concern if we’re dead or crippled. Don’t let them shame you into giving over your precious and delicate shell to medical scientific experimentation by companies that are incapable of taking accountability for their actions. This is the core argument that you need to keep at the forefront of any debate, rather than whether your DNA is permanently changed or whether its functions are just altered. If you’re going to get into the gutter to battle out the science then you must get your facts straight. They will use any potential misunderstanding you have to wipe your voice from the debate. It is they who bear the burden of articulating clearly why we should take the vaccine; it is your right to refuse.

However, there is something no one has mentioned so far about this new mRNA technology that could give those who oppose the vaccine another way out. Normally, to be effective, a vaccine must be given to as much of the population as possible. Mass vaccination has been used historically as a synthetic herd immunity to stop the spread of a virus to the vulnerable people in our society. But this technology is different, and its method of working means it is no longer necessary to use mass vaccination.

The whole point of why mRNA vaccines are more effective than our current vaccine technologies, per its proponents, is that it precisely targets the protein-production part of your DNA’s normal life cycle. This improves the response that an individual’s immune system will have when fighting a virus. It can be targeted socially in a similar way. If the majority of people who catch Covid-19 are asymptomatic, then it’s ridiculous to give them a vaccine. Because this vaccine protects individuals in their response, there is no good reason why everybody in our society should be forced to take it. It is used to increase specific protein production in someone who’s at severe risk—that’s how a medicine works normally. You don’t take HIV medication if you don’t have HIV. You shouldn’t be taking cancer drugs unless you have cancer. And you shouldn’t need to change your DNA’s production of specific proteins unless it’s personally necessary to do so.

The biggest lie being told to the people of the world is that everybody needs to take this vaccine. And ironically, the experimental mRNA technology that they’re desperate to use makes mass vaccination unnecessary.