COVID-19 Vaccine « Aletho News

10 Facts From the UK Government Pfizer Vaccine Guidance that Promote “Vaccine Hesitancy”

By Johnny Vedmore | ~~Unlimited Hangout~~ | December 29, 2020

Official government guidance has been released in the United Kingdom to assist healthcare professionals in administering the Pfizer/BioNTech vaccine BNT162b2. While the UK government goes to war against supposed misinformation, the official narrative is clearly based on very little to no supporting data from incomplete clinical trials. This article examines the document “Reg 174 Information for UK Healthcare Professionals” and narratives being pushed in the mainstream media that directly contradict that document.

Healthcare professionals globally have begun the controversial campaign to vaccinate large swathes of their respective populations with various experimental medical products. The vanguard of the mainstream pro-vax extremists have been busy enacting mass censorship tactics and committing blatant acts of digital book burning on a scale never before seen in the internet era. So-called “trusted sources” have become indistinguishable from the state-run media apparatus of your bog-standard dictatorship with the usual MSM outlets working non-stop to skew any information that threatens their hyper-aggressive official narrative. Throughout 2020, our basic civil liberties have been quickly stripped away by countless unelected officials from a wide array of unaccountable global power structures, all of them connected to a small group of elites who are sitting aloft the COVID-19 money train and using the heavily exaggerated epidemic to achieve their own long term goals.

Any useful data, scientific paper, or other credible research contradicting the official narrative is being purposely hidden from view. Too many uncomfortable, yet ultimately necessary, questions for vaccine companies such as Moderna, AstraZeneca, Pfizer, and their many collaborators, are being heavily censored by those pushing their own various COVID-related agendas. The promised “war on truth” is in full swing throughout all nations globally and their respective state media machines are nearly all towing their official government lines. Mainstream talk shows and podcasts worldwide are also in lockstep, and have often been caught publicly guilt-tripping their easily swayed audiences to help push them deeper into queues for mass medical trials for vaccines and other products that lack research studies on their long term effects. This inconvenient lack of completed research will not stop the money men from pumping this milky white liquid into the arms of hundreds of millions of people worldwide.

At this point in the process, the medical professionals who are administering these heavily rushed vaccines are being given the opportunity to defer responsibility and accountability for their actions to the government’s vaccine-related guidance. As the Stanley Milgram experiments have proven, when the option to defer responsibility is present, then roughly 65% of participants will follow the orders they have received regardless of the risk to their subjects. In 1974, Stanley Milgram detailed the behaviour of his participants in his famous study and suggested that people have two basic states of behaviour when they are in a social situation: “The autonomous state”, where people direct their own actions and ultimately take responsibility for the results of those actions and “the agentic state”, where people allow others to direct their actions and then pass off the responsibility for the consequences to the person giving orders, in essence acting as agents of another person’s will.

The majority of the people who are injecting these experimental drugs into their trusting patients are not likely to question the official guidance, as the overwhelming majority will often simply be in an agentic state. Thus, it should be in the best interest of anyone thinking of receiving an mRNA vaccine to first study the guidance offered by the various government sources. And, when one does study the official guidance given to healthcare professionals, one will find many different glaring contradictions and shocking admissions.

While all official bodies are attacking any inconvenient fact as misinformation, they are all busy defrauding the global population with their own misinformation campaigns that surely would have inspired awe in the likes of Joseph Stalin. So, let’s study their own words and examine the NHS guidance given to the medical professionals in the UK for the administration of the recently approved Pfizer-BioNTech vaccine.

An Introduction to Reg 174 Information for UK Healthcare Professionals (#1-4)

The short ten page official guidance being given to UK healthcare professionals contains many interesting admissions. In fact, the document, released in early December 2020 to accompany the vaccine rollout, appears to advise healthcare practitioners not to risk giving the experimental injection to the majority of the people who are due to receive the vaccine, particularly “prioritized” populations. Those in charge are pushing to vaccinate as much of the population as possible, before any critical public questions can be asked and answered, a situation that has left the safety and ethics of the vaccination campaign questionable at best and inhumane at worst.

In going through the Reg 174 document, it becomes very clear that there are many issues and recommendations that are being hidden from the general public. Here are ten of the most notable causes for concern contained within the official UK guidance document.

1. This medicinal product does not have UK marketing authorisation but has been given authorisation only for temporary supply

The authorisation to produce and supply this experimental vaccine in the UK was given by the UK Department of Health and Social Care, led by Matt Hancock – the UK Secretary of Health, and also by the Medicines & Healthcare products Regulatory Agency (MHRA). While the MHRA is part funded by the Department of Health and Social Care for the regulation of medical devices, the costs of medicine regulations are met through fees paid by the pharmaceutical industry. The agency’s financial reliance on Big Pharma has led to suggestions by some Members of the UK Parliament that the MHRA is not actually independent. Being in associated roles at the MHRA since 1985, June Raine was officially appointed as CEO in September 2019 and had previously been the Director of Vigilance and Risk Management in the Medicines Division.

2. The official Phase III safety trials will not be completed until 2023

Section 1 of the medical guidance clearly states that this vaccine guidance refers specifically to the “Pfizer/BioNTech COVID-19 mRNA Vaccine BNT162b2 concentrate for solution for injection.” On 2 December 2020, the MHRA became the first medicines regulator in history to approve an mRNA vaccine for human use, granting emergency authorisation for BioNTech and Pfizer’s BNT162b2 COVID-19 vaccine for widespread use only a week after its first Phase III eight-week trial had finished. However, the Phase III trials for BNT162b2 will not actually be fully completed until January 2023 meaning that, if you’re ready to take the vaccine now, then you should be informed that the safety trials for these experimental vaccines have at least two more years before the results are in. Regardless of that fact, Raine told reporters “no corners have been cut in approving it” and that “the benefits outweigh any risk”.

3. Will you be truly “protected” from COVID-19?

The official guidance clearly states that individuals may not be protected until at least 7 days after their second dose of the vaccine. This fact has again been ignored by various reckless pro-vax media campaigns where powerful elites such as Tony Blair have contradicted this specific recommendation, suggesting recently in an interview that people should only be given a single dose of any vaccine. Mr Blair told BBC Radio 4’s Today programme that “Does the first dose give you substantial immunity, and by that I mean over 50 percent effectiveness? If it does, there is a very strong case for not, as it were, holding back doses of the vaccine.” Blair, writing in the Independent, stated that the current vaccination strategy needed to be “altered and radically accelerated”. In responding to Blair’s call for radical acceleration, Professor Wendy Barclay, chair of virology at Imperial College London and member of the UK government’s NERVTAG, said: “I think that the issue with [Mr Blair’s suggestion] is that the vaccine is on the basis of being given in two doses, and the efficacy is on that basis.” Barclay went on to point out that “To change at that point, one would have to see a lot more analysis coming out from perhaps the clinical trial data.”

It is very important to pay attention to the wording of Reg 174 because the Pfizer vaccine purportedly boosts the immune system, rather than stopping the transmission of the virus. This would suggest that you will not be fully “protected” from COVID-19 and that you will still be able to catch the virus and could still suffer complications. The official guidance also states that “Immunocompromised persons, including individuals receiving immunosuppressant therapy, may have a diminished immune response to the vaccine,” with the guidance admitting “No data are available about concomitant use of Immunosuppressants.”

Reg 174 goes on to make this most pertinent of points when it states “As with any vaccine, vaccination with COVID-19 mRNA Vaccine BNT162b2 may not protect all vaccine recipients.” The guidance also states clearly that “administration of COVID-19 mRNA Vaccine BNT162b2 should be postponed in individuals suffering from acute severe febrile illness and that individuals receiving anticoagulant therapy or those with a bleeding disorder that would contraindicate intramuscular injection, should not be given the vaccine unless the potential benefit clearly outweighs the risk.”

4. The complicated multistage dilution and thawing process of the vaccine vials opens the major possibility of human error

In investigating the official instructions for the vaccine’s administration, we can clearly see that there are plenty of opportunities for potential human error. Section 2 of this document describes the distributed vaccine as coming in “a multidose vial and must be diluted before use.” Confirming that each vial contains 0.45 ml (which equates to 5 doses of 30 micrograms) of BNT162b2 RNA embedded in lipid nanoparticles. The delicate preparation process will be repeated 100s of millions of times globally and the multidose vial will be stored frozen and must be thawed prior to dilution. The guidance describes the process for preparing the frozen vials stating that they should be transferred to temperatures of between 2 °C to 8 °C to thaw or, alternatively, the frozen vials may also be thawed for 30 minutes at temperatures up to 25 °C for immediate use. Once thawed, the undiluted vaccine can be stored for up to 5 days at 2 °C to 8 °C, and up to 2 hours at temperatures up to 25 °C. The thawed vial must then come to room temperature and be gently inverted 10 times prior to dilution.

Some of the featured diagrams and instructions found in Reg 174

The complicated thawing and dilution process will obviously leave room for individual error. Healthcare practitioners are also warned not to shake the vials and instead to gently turn them 10 times. Prior to dilution, the vaccine should present as an off-white solution with no particulates visible. The guidance states that you must discard the vaccine if particulates or discolouration are present. The thawed vaccine must be diluted in its original vial with 1.8 mL sodium chloride 9 mg/mL (0.9%) solution for injection, using a 21 gauge or narrower needle and aseptic techniques and this complex, multistage process isn’t completed there.

The healthcare professional should then equalise vial pressure before removing the needle from the vial by withdrawing 1.8 mL of air into the empty diluent syringe. Then they should gently invert the diluted solution 10 times, again being careful not to shake the solution. The official guidance continues: “The diluted vials should be marked with the dilution date and time and stored between 2 °C to 25 °C. After dilution, the vial contains 5 doses of 0.3 mL.” The healthcare professionals are then told to “withdraw the required 0.3 mL dose of diluted vaccine using a sterile needle and syringe and discard any unused vaccine within 6 hours after dilution.”

The instructions must be followed precisely to safely administer the mRNA vaccine; there are no data available on potential consequences for the vaccine recipient if anything goes wrong during this tedious and complex multistage process. On 19 December 2020, video emerged of an official drive-thru vaccination hub which had begun operating out of a car park of Hyde Leisure Centre in Greater Manchester. The video in question, shared by No Comment TV on YouTube, shows people being vaccinated outdoors at Hyde Leisure Centre by gloveless staff and in less than sterile conditions. In an article in the Manchester Evening News four days prior to the videos release the local news site stated that “The first batch of the Pfizer/BioNTech vaccine arrives in the borough on Tuesday, with vaccinations starting at Hyde Leisure Centre on Wednesday, December 15.”

No Data Available (#5-10)

When reading Reg 174, you will soon notice a recurring theme throughout the document. The guidance clearly states on multiple occasions that there are no data available concerning some of the most important questions surrounding the mRNA vaccine. As previously noted, the actual Phase III section of the safety trials will not be completed until January 2023, meaning that two years of trials are still to be run before the vaccine can be confirmed as safe, effective and ethical.

5. The safety and efficacy of COVID-19 mRNA Vaccine BNT162b2 in children under 16 years of age have not yet been established

Although the guidance states that the safety and efficacy of the COVID-19 vaccine has not been established in children, it doesn’t mean that children have not been included within the studies. In fact, in the official Pfizer study entitled “Protocol C4591001”, one of the two main study groups included children as young as 12 years old. The inclusion of children in trials but not the guidance raises the important question, why were children included in the trial? If the vaccine is not to be given to those under the age of 16 years old, then why include children as young as 12 in the trials for an experimental vaccine technology never before authorised for use in humans?

The mainstream media, instead of raising concerns about the involvement of children in the Pfizer clinical trials, have been fully supportive of the move to test experimental pharmaceuticals on minors. CNN reported on children as young as 12 being involved in trials in an October 2020 article entitled “This 12-year-old is happy to be testing a Covid-19 vaccine” while Microsoft News recently announced that “China begins Covid test trials on children as young as age three.”

6. No data are available on the use of COVID-19 mRNA Vaccine BNT162b2 in persons that have previously received a full or partial vaccine series with another COVID-19 vaccine

We are currently witnessing the very first of many tailor-made vaccines being rolled out for general use, so don’t expect the COVID-19 jabs to be the only vaccines coming our way. With a 20 to 1 return on investment on many of these new technologies, most pharmaceutical giants will surely be lobbying governments across the globe for the next “necessary” vaccination program. The idea of multiple COVID-19 vaccinations throughout the year is already being presented as a very possible outcome for the future of humanity. Yet, no studies have been completed showing the risk of taking different types of vaccines. There have also been suggestions that people will have to have the same vaccine that they had previously taken every six months or so. This will leave Astrazeneca, Pfizer and Moderna picking up repeat vaccine contracts worth billions in secured future revenue before there are any real data on the results of the vaccines.

7. No interaction studies have been performed and there are no, or a limited amount of, data from the use of COVID-19 mRNA Vaccine BNT162b2

Admissions like these should be a cause for concern for anybody reading the official guidance. While officials and carefully chosen “trusted sources” are telling you that “no corners have been cut” in the race to approve these vaccines, it is also true that no full length studies have been completed either. These two facts are juxtaposed and obviously contradict the official narrative that is being thrust upon the general public by all of those involved.

It is clear that the officials have no real data on what will happen next and that there is a tsunami of ethical questions that are not being answered. In the absence of data, there will be speculation.

8. It is unknown whether COVID-19 mRNA Vaccine BNT162b2 is excreted in human milk and It is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility

It is vital to note the potential dangers posed by the BNT162b2 to unborn and newborn babies as well as the reproductive organs in general. There are so many parts of the Pfizer/BioNTech clinical trials that have not yet been completed. Dr. Peter Klatsky, the Director of Fertility Preservation at the Bay Area’s Spring Fertility, talking about the coming animal trials which are to be performed over the coming months was quoted in SFGate as saying, “It will reassure me an awful lot if the protein expression is not seen on the placenta. That the mRNA isn’t making it to the placenta in animals,” he said. “I don’t expect to see any.” The article goes on to explain that it will be about another 9 months until the data has been collected and analyzed.

Section 4.6 of the official guidance recommends pregnant women should not recieve the BNT162b2 vaccine

Big names in mainstream media have also been caught recklessly promoting the vaccine to pregnant women, such as Karen Weintraub writing for USA Today, whose recent article quickly states, “Although there are very little data on how pregnant and nursing mothers will respond to a COVID-19 vaccine, professional organizations and individual doctors say the benefits are very likely to outweigh the risks.” Even though the clinical trials intentionally excluded pregnant women, Weintraub went on to state that “23 women in the Pfizer-BioNTech trial and 13 in Moderna’s became pregnant during the trial.”

While the UK’s official guidance is left sounding ambiguous, on the European continent, the European Medicines Agency (EMA) states that “the Pfizer vaccine should be considered on a case by case basis for pregnant women”, but they also reserve the right to alter the guidance if more data becomes available. It seems there is no longer any erring on the side of caution with some regulators when it comes to the COVID-19 vaccinations.

9. Non-clinical data reveal no special hazard for humans based on a conventional study of repeat dose toxicity but animal studies into potential toxicity to reproduction and development have not been completed

Animal studies have not been completed and, as referred to in the previous section, the data on those animal trials will not be available for another 9 months. It is, of course, a very rare decision to approve an experimental medical technology before any animal studies have been completed. This should be a great cause for concern for any free thinking man or woman. The fact that they have had to use what they refer to as “non-clinical” data in these studies is also in conflict with the idea that the trials were conducted to the highest professional standard. The document also fails to clearly define what non-clinical data actually means.

10. In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products

Possibly the most fascinating admission in the entire document is the absence of any compatibility studies when somebody is given the vaccine while on any other medication or medical treatment. The guidance clearly states “this medicinal product should not be mixed with other medical products.” This completely jaw dropping sentence will lead many to assume that if you are on any medication at all, then you shouldn’t be given the vaccine. Whether this refers to the mixing of other medical properties directly together with the vaccine, or simultaneous dosing of any other medical product is unclear from the official guidance.

The Mail Online and The Guardian reported in 2019 that a staggering 1 in 4 people in England – nearly 12 million people – were taking what was described as “addictive” prescription medicines such as antidepressants, sleeping pills and opioid painkillers, saying that “the NHS must take action”. Those statistics throw into question the mass rollout of a vaccination with no compatability studies. This makes the fact that elderly care home residents, followed by those aged over 80, will be the first to recieve the experimental Pfizer vaccine an extremely risky strategy. Also in 2019, Age UK reported that nearly 2 million older people were on more that 7 prescription medicines and were at “risk of side effects that are severe in some cases, and occasionally even life threatening.” This worrying issue has been barely reported by the “trusted news sources”.

A Conclusive Lack of Real Data

After examining the official guidance, one fact becomes glaringly obvious — there is little to no data on the official Pfizer vaccine in key areas. In the clinical trials, children as young as 12 years old were used as unnecessary guinea pigs. There also wasn’t enough care taken to avoid pregnant women being involved in the initial clinical trials and under the cover of unyielding and uneducated mainstream propaganda, the safety of some of the most vulnerable people involved in the vaccine trials have been ignored by Pfizer and the politicians who have successfully pushed for the public vaccination campaign to essentially replace mass clinical trials. The stage has been set for a potential disaster on an unimaginable scale. It isn’t only the participants of the trials who are risking their health for the sake of big pharmaceutical companies’ hyperinflated profit margin, but it is also the medical professionals who could be risking their futures by collaborating in these risky experimental trials, which will certainly see many people dead and irreversibly injured.

In one section of Reg 174, the Big Pharma giant lays out the risk to people’s health from the Pfizer/BioNTech vaccine. The most common adverse reaction in participants 16 years of age and older was pain at the injection site, which affected a massive 80% of those taking part in the Pfizer trials. Fatigue came a close second with 60% of trial participants becoming sluggish and tired. Half of those involved in the studies suffered from a headache as the experimental vaccine went to work while myalgia was experienced by 30% of vaccine recipients, though the results do not indicate whether the myalgia was acute (short-term) or chronic (long-term). Almost a third of participants came down with chills, while just under 1 in 5 people suffered from arthralgia (joint pain) and 1 in 10 from pyrexia (increased body temperature).

Adverse reactions reported in clinical trials are listed in the study in decreasing order of frequency and seriousness. Just under 1 in 10 people who take the vaccine will suffer from the very common and common adverse reactions referred to in the latter paragraph, such as headaches, myalgia and chills, but the more serious issues are classified as uncommon – including Lymphadenopathy (which causes swollen or enlarged lymph nodes) and nervous system disorders – which may affect up to 1 in 100 people. Rare adverse reactions that could affect up to 1 in 1000 people and very rare adverse reactions that would affect less than 1 in 10,000 of the vaccine recipients were not included in Pfizer’s self-reported safety information. It has obviously been decided that this information should be kept out of the public domain as much as possible to avoid any further vaccine hesitancy.

Not only does the official guidance actively hide the types of rare and very rare adverse effects, but they have also been leaving out some of the adverse reactions reported during the clinical trials. As I write this, the Reg 174 guidance for healthcare professionals is on version 10.1 of the document and, since its release, they have yet to admit to the potential of a certain uncommon adverse reaction to the vaccine being a specific nervous system disorder. Structural nervous system disorders include brain or spinal cord injury, Bell’s palsy, cervical spondylosis, carpal tunnel syndrome, brain or spinal cord tumors, peripheral neuropathy, and Guillain-Barré syndrome. However, previous versions of the guidance gives no clue as to what type of nervous system disorders they were referring to. However, recent articles in the USA Today, heavily promoted by the Microsoft Network, suggested that the Bell’s palsy some people came down with in the vaccine trials wasn’t related to the Pfizer jab. The article states that on Dec. 10, the FDA’s Center for Biologics Evaluation and Research held the 162nd meeting of the Vaccines and Related Biological Products Advisory Committee to discuss the emergency use authorization of the Pfizer-BioNTech COVID-19 vaccine. The USA Today piece even goes on to admit that , “a 53-page briefing noted that there had been four cases of Bell’s palsy among the vaccinated group and none among the placebo group.”

Bell’s palsy causes drooping facial muscles similar to the effects of a stroke, image source PTHealth.com

Even though Miriam Fauzia, who wrote the USA Today piece, claims that the Bell’s palsy was not related to the experimental Pfizer vaccine, the 53-page briefing she sources clearly states, “Among non-serious unsolicited adverse events, there was a numerical imbalance of four cases of Bell’s palsy in the vaccine group compared with no cases in the placebo group, though the four cases in the vaccine group do not represent a frequency above that expected in the general population.” While it is true that 1 to 4 people in 10,000 will develop Bell’s palsy within the general population, it should be noted that the 4 cases in the vaccine trials and none in the placebo group makes for a statistical anomoly that must be examined more thoroughly. Instead, the mainstream media moved quickly to discredit the Bell’s palsy links to the Pfizer vaccine using various misleading tactics to achieve their aims.

Many mainstream outlets were caught spouting the same misleading information with articles entitled “Why you shouldn’t worry about a connection between Bell’s palsy and COVID-19 vaccines,” from Business Insider and a Reuters article from 14 December 2020 entitled, “Fact check: Photo does not show three recipients of Pfizer’s COVID-19 vaccine that developed Bell’s palsy.”

In the case of the Reuters article, which is described as written by “Reuters Staff” rather than a specific journalist, the focus was not on the four Pfizer clinical trial participants who developed Bell’s palsy but instead the article discredits a random post on social media of three people with Bell’s palsy unconnected to the Pfizer vaccine. These type of misinforming mainstream media articles are commonly found to be using obvious fallacies to mislead their readership and with no individual taking responsibility for writing the misinforming piece, a trick repeated by many other media companies complicit with the official narrative. The Reuters article even goes on to admit that: “According to the FDA’s briefing document dated December 10, Bell’s palsy was reported in four vaccine participants and none in the placebo group, out of the 44,000 total participants of the late-stage vaccine trial.” However, the title of the Reuters article would mislead even some of the most keen eyed observers.

The mainstream media has been creating a flood of misleading stories, but it appears as though they have been given carte blanche to continue to do so, probably because they are sticking so tightly to the official narrative. It’s a narrative that is thick with irony, for it is the “trusted sources” who are being caught systematically misleading the general population again and again while also declaring a propaganda war against “fake news”.

The official guidance noted in Reg 174 doesn’t only highlight the serious lack of real data gained from Pfizer’s clinical trials for its Covid-19 vaccine so far, but it also exposes the wealthy medical professionals involved in these experimental vaccine development programs as complacent, reckless and very naive. It’s no secret that children are, more often than not, incapable of giving informed legal consent for such a risky and unethical enterprise. But the pro-vax extremists are using every tactic to coerce and manipulate children and their guardians into becoming human guinea pigs for Big Pharma. Pregnant women are also treated as acceptable collateral damage to advance the new science of gene, mRNA and DNA manipulation, a science and technology that pushes a sinister transhumanist agenda.

Don’t be fooled by the carefully worded vacuous celebrities, self-serving politicians, Big Pharma, and the mainstream medias authoritarian style misinformation campaigns. Keep your humanity intact and read their own words. The government guidance to healthcare professionals clearly states on multiple occasions that there are “no data available”.

Johnny Vedmore is a completely independent investigative journalist and musician from Cardiff, Wales. His work aims to expose the powerful people who are overlooked by other journalists and bring new information to his readers. If you require help, or have a tip for Johnny, then get in touch via johnnyvedmore.com or by reaching out to johnnyvedmore@gmail.com

December 29, 2020 Posted by aletho | Deception, Fake News, Full Spectrum Dominance, Mainstream Media, Warmongering, Science and Pseudo-Science, Timeless or most popular | COVID-19 Vaccine, UK, USA Today | Leave a comment

2020: The Year We Lost Our Common Sense, Courage and Civil Liberties

By Robert Bridge | Strategic Culture Foundation | December 28, 2020

Once it became clear to the Western elite that their subjects would readily accept draconian anti-Covid measures, it encouraged them to usher in a code-red lifestyle where there will be no ‘return to normal’ in the foreseeable future and, possibly, ever.

If nothing else, nobody can say we were not warned about the madness that would descend upon leap year 2020, making it one of the worst 366 days ever recorded on the Gregorian calendar.

On October 18, 2019, the Johns Hopkins Center for Health Security, together with the World Economic Forum and the Bill and Melinda Gates Foundation hosted the incredibly visionary Event 201, an exercise that simulated the outbreak of a pandemic “transmitted from bats to people that eventually becomes… transmissible from person to person.”

The simulation proved to be so uncannily similar to the real thing that started just three months later – from imagining a dramatic drop in air travel and business, to breaks in the global supply chain – that Johns Hopkins eventually felt compelled to release a statement saying their exercise was not intended to be a prophecy of future events.

“To be clear, the Center for Health Security and partners did not make a prediction during our tabletop exercise,” the statement read, in what just might be the creepiest caveat ever. “For the scenario, we modeled a fictional coronavirus pandemic, but we explicitly stated that it was not a prediction… We are not now predicting that the nCoV-2019 outbreak will kill 65 million people.”

Shortly after the global elite played Nostradamus, on January 15^th to be exact (the very same day, incidentally, that the Democrats presented articles of impeachment against President Donald Trump in the Senate), the first Covid-positive person arrived in Seattle from Wuhan, the Chinese city where the disease is said to have sprung to life. From there it has been a non-stop roller-coaster ride of government-sponsored insanity.

Before continuing, it is important to remember the context with which the pandemic has been happening, that is, in the most consequential U.S. presidential election in recent memory. It should thus come as no surprise that the Democrats and Republicans would use the scourge to achieve some sort of advantage, demonstrating Machiavellian opportunism at its very best. Indeed, such is the nature of the political beast.

For example, although Trump shut down the U.S. border on January 31 to Chinese nationals, the Democrats and leftist media pounced, saying the U.S. leader responded too late to make a difference. Even Trump’s use of the term ‘Chinese virus’ was slammed by his opponents as ‘racist.’ Meanwhile, it was the Democrats themselves who were the pioneers in taking the first draconian steps of locking down society to stop the contagion.

On March 16, 2020, six counties in northern California and the city of Berkley ordered an unprecedented stay-at-home order for some 7 million Bay Area residents. This was all part of “flattening the curve” logic that would “buy time for hospitals to gear up for the onslaught…” Well, 233 days later political leaders are not only still flattening the curve, but flattening their economies as well. Today, although the survival rate for those infected with Covid-19 is reported to be in the neighborhood of 99.85 percent, harsh lockdowns continue to wreak havoc, not least of all for small businesses.

This is criminal. Complete BS!!! I guess this is “science”! RT @ClayTravis: Watch this video of an LA bar owner that perfectly crystallizes the absurdity of California’s absurd and ridiculous shutdown rules. pic.twitter.com/XVLmAVyy70

— Larry The Cable Guy (@GitRDoneLarry) December 5, 2020

Consider the situation in California, where Governor Gavin Newsom has mandated yet another ‘shelter-in-place’ order, which has shuttered, among other businesses, hair salons, barbershops, personal care services, movie theaters, wineries, bars, breweries, family entertainment centers and amusement parks. What is hard to fathom, however, is how the corporate big-box stores are considered “essential businesses,” apparently immune to the scourge, while the small business owner is trashed as expendable.

By way of example, consider the tragic plight of Angela Marsden, the owner of Pineapple Hill Saloon and Grill in Los Angeles. In an effort to comply with the ever-changing anti-Covid rules, Marsden spent over $80,000 to build an outdoor patio so she could stay in business during the pandemic. With Newsom’s latest lockdown restrictions, however, city officials denied her permission to serve clients on location, even in the parking lot.

To add insult to injury, the authorities granted permission for a film company to set up a large outdoor eating area for its staff just across the road from where Marsden had built her patio.

“I’m losing everything,” she exclaimed in a video posted to Twitter that has been watched almost 10 million times. “Everything I own is being taken away from me. They have not given us money and they have shut us down. We cannot survive; my staff cannot survive…”

For the Fortune 500 companies, however, the pandemic has translated into a windfall. Between April and September, at a time when thousands of small business were quietly getting crushed underfoot, 45 of the 50 most valuable publicly traded American companies turned a profit, according to the Washington Post.

At the same time, at least 27 of the 50 largest firms slashed their workforce this year, collectively cutting more than 100,000 workers, while at the same time distributing billions of dollars to shareholders. As just one example, Walmart distributed more than $10 billion to its investors during the pandemic while terminating 1,200 office staff.

To put these figures another way, since mid-March – when President Donald Trump declared a national emergency – America’s 614 billionaires saw their net worth explode by $931 billion in total. Jeff Bezos, for example, the founder and chief executive of Amazon, saw his private wealth go from $73.2bn since the start of the crisis to a record $186.2bn.

It would probably come as no surprise that the very individuals who helped pave the way for astronomic wealth generation among the 1 percent, are the same ones breaking their own rules. Governor Newsom and his wife, for example, attended a birthday party with a dozen friends at the French Laundry restaurant in San Francisco. Equally maddening is that Dustin Corcoran, the CEO of the California Medical Association, was also in attendance. And who could forget the photo of Nancy Pelosi walking through a California hair salon when such businesses were deemed ‘super spreaders’?

https://twitter.com/PatrioticCandor/status/1334313479315009538?ref_src=twsrc%5Etfw%7Ctwcamp%5Etweetembed%7Ctwterm%5E1334313479315009538%7Ctwgr%5E%7Ctwcon%5Es1_&ref_url=https%3A%2F%2Fwww.strategic-culture.org%2Fnews%2F2020%2F12%2F28%2F2020-the-year-we-lost-our-common-sense-courage-and-civil-liberties%2F

Such incidences only served to reinforce the idea that the draconian lockdowns, the worst of which are centered on Democratic-controlled states, were specifically designed not to contain a contagion, but to foster as much anger and frustration among the general population in the most consequential presidential election in many decades. After all, unhappy people have a tendency to vote out their leaders whom they believe are responsible for such dire circumstances. And with the mainstream media almost totally in the Democratic anti-Trump camp, placing the blame on the president has proven no difficult task.

So where do we go from here? Now that we have reached the end of 2020, will the situation begin to improve? Will political leaders begin to loosen the screws and let some semblance of normality return once again? Or will people be forced to rise up and demand the return of their freedom and liberty?

At this great loggerhead in human history, there has been much talk about creating ‘freedom passes’ that will be demanded from people before they are allowed to travel or visit any sort of entertainment again.

“People who test negative for coronavirus could get a five-day freedom pass to attend big events or access public buildings, under plans being considered by public health experts running a trial program in England,” reported Bloomberg in November.

Already, five global airlines – United Airlines, Lufthansa, Virgin Atlantic, Swiss International Air Lines and JetBlue – have announced they will observe the so-called CommonPass to passengers on some flights from December.

“The project, developed by non-profit group The Commons Project and backed by the World Economic Forum, uses a digital certificate downloaded to a mobile phone to show a passenger has tested negative for Covid-19,” according to the Financial Times. Here is the kicker: “The airlines are not making the CommonPass mandatory, but in time it will also be used to provide proof of vaccination.”

It seems rather obvious where all of this is heading: mandatory vaccination for anyone who ever wishes to board an aircraft or visit another entertainment venue again. Over time, it is not difficult to imagine a vaccine regimen extending to all human activities, including shopping and even getting a job. Yet what about the millions of people who have expressed extreme skepticism in being administered a vaccine that has been developed so quickly?

Whatever the case may be, should such a plan of action become mandatory, peoples’ lives will be entirely dominated by fears over a virus, together with an endless bureaucratic process of being tested and approved to move about. Vaccines will become a regular requirement since viruses are in a state of constant mutation, which makes them the authoritarian’s dream instrument of domination.

Such a system of totalitarian control, should it ever come into fruition, will have achieved in mere months what fascism could not in years: the pacification and unification of a great swath of the world’s population not by bayonet, but by syringe. In fact, today the people of London are fleeing their fair city not out of fear of the virus per se, but out of fear of the lockdown restrictions put in place by the authorities. To put it otherwise, the world gave an inch and the globalists took a mile, and a person would have to be a fool to believe it could have turned out any other way.

December 28, 2020 Posted by aletho | Civil Liberties, Economics, Supremacism, Social Darwinism, Timeless or most popular | Covid-19, COVID-19 Vaccine, Event 201, United States, Walmart, World Economic Forum | Leave a comment

Major Covid Vaccine Glitch Emerges: Most Europeans, Including Hospital Staff, Refuse To Take It

By Tyler Durden | Zero Hedge | December 27, 2020

All is not going according to plan in the biggest global rollout of what is arguably the most important vaccine in a century, and it is not just growing US mistrust in the covid injection effort that was rolled out in record time: an unexpected spike in allergic reactions to the Pfizer/BioNTech vaccine (and now, Moderna too) may prove catastrophic to widespread acceptance unless scientists can figure out what is causing it after the FDA’s rushed approval, and is also why as we reported yesterday, scientists are scrambling to identify the potential culprit causing the allergic reactions.

Making matters worse, Europe rolled out a huge COVID-19 vaccination drive on Sunday to try to rein in the coronavirus pandemic but even more Europeans than American are sceptical about the speed at which the vaccines have been tested and approved and reluctant to have the shot.

While the European Union has secured contracts [with] drugmakers including Pfizer, Moderna and AstraZeneca, for a total of more than two billion doses and has set a goal for all adults to be inoculated next year, this is looking increasingly like a pipe dream: according to recent surveys, the local population has expressed “high levels of hesitancy” towards inoculation in countries from France to Poland, with many used to vaccines taking decades to develop, not just months.

“I don’t think there’s a vaccine in history that has been tested so quickly,” Ireneusz Sikorski, 41, said as he stepped out of a church in central Warsaw with his two children.

“I am not saying vaccination shouldn’t be taking place. But I am not going to test an unverified vaccine on my children, or on myself.”

Smart: why take the risk of getting vaccinated when others will do it, resulting in the same outcome.

Surveys in Poland, where distrust in public institutions runs deep, show that fewer than 40% of people planning to get vaccinated. Worse, according to Reuters on Sunday, only half the medical staff in a Warsaw hospital where the country’s first shot was administered had signed up. And if the doctors don’t trust the vaccine, one can be certain that the broader population will refuse to take it.

The situation is similar in Spain, one of Europe’s hardest-hit countries, where 28-year-old singer and music composer German summarizes the skepticism of a broad range of the population, and plans to wait for now.

“No one close to me has had it (COVID-19). I’m obviously not saying it doesn’t exist because lots of people have died of it, but for now I wouldn’t have it (the vaccine).”

A Christian Orthodox bishop in Bulgaria, where 45% of people have said they would not get a shot and 40% plan to wait to see if any negative side effects appear – meaning only 15% of the population will actually volunteer for a vaccine in the near future – is in the tiny minority when it comes to taking the vaccine.

“Myself, I am vaccinated against everything I can be,” Bishop Tihon told reporters after getting his shot, standing alongside the health minister in Sofia. He spoke about anxiety over polio before vaccination became available in the 1950s and 1960s.

To be sure, the establishment is pounding the table on why the vaccines are safe despite the record short time in development (even though not even the “scientists” can explain what is behind the spike in vaccine allergic reactions), and claiming that the new technology behind the mRNA vaccine is all one needs to know… when it is precisely this new technology that is sparking the skepticism.

“We’ll look back on the advances made in 2020 and say: ‘That was a moment when science really did make a leap forward’,” said Jeremy Farrar, director of the Oxford University Clinical Research Unit, which is backed by the Wellcome Trust. Oxford also received $750MM from Bill Gates in June in the billionaire’s quest to vaccinate the world against Covid.

Only problem: nobody in Europe seems to care about these “scientific” justifications. Independent pollster Alpha Research said its recent survey suggested that fewer than one in five Bulgarians from the first groups to be offered the vaccine – frontline medics, pharmacists, teachers and nursing home staff – planned to volunteer to get a shot.

An IPSOS survey of 15 countries published on Nov. 5 showed then that 54% of French would have a COVID vaccine if one were available. The figure was 64% in Italy and Spain, 79% in Britain and 87% in China.

Since then things have gone far worse, and a more recent IFOP poll showed that only 41% people in France would take the shot. This means that a vast majority will not.

Not even in Sweden, where public trust in authorities is absurdly and inexplicably high, is there a universal trust in the vaccine, with at least one in three saying they won’t get the shot: “If someone gave me 10 million euro, I wouldn’t take it,” Lisa Renberg, 32, told Reuters on Wednesday.

Meanwhile, in a paradoxical attempt to force more to sign up – not realizing that it will only have the precisely opposite effect – Polish Prime Minister Mateusz Morawiecki urged Poles on Sunday to sign up for vaccination, saying the herd immunity effect depended on them. Critics have accused Warsaw’s “nationalist leaders” of being too accepting of anti-vaccination attitudes in the past in an effort to garner conservative support. Well… let’s check back on said attitude in 10 years and see if perhaps it was the right one.

For now, however, the more European governments pressure their populations to get immunized, the fewer the people who will actually sign up and the worse the vaccine rollout will be, that much we can be 100% sure of.

December 27, 2020 Posted by aletho | Aletho News | COVID-19 Vaccine | Leave a comment

Developers of Oxford-AstraZeneca Vaccine Tied to UK Eugenics Movement

By Jeremy Loffredo and Whitney Webb | ~~Unlimited Hangout~~ | December 26, 2020

The developers of the Oxford-AstraZeneca vaccine have previously undisclosed ties to the re-named British Eugenics Society as well as other Eugenics-linked institutions like the Wellcome Trust.

On April 30th, AstraZeneca and Oxford University announced a “landmark agreement” for the development of a COVID-19 vaccine. The agreement involves AstraZeneca overseeing aspects of the development as well as manufacturing and distribution while the Oxford side, via the Jenner Institute and Oxford Vaccine Group, researched and developed the vaccine. Less than a month after this agreement was reached, the Oxford-AstraZeneca partnership was awarded a contract from the US government as part of Operation Warp Speed, the public-private COVID-19 vaccination effort dominated by the US military and US intelligence.

Though the partnership was announced in April, Oxford’s Jenner Institute had already begun developing the COVID-19 vaccine months before, in mid-January. According to a recent BBC report, it was in January that the Jenner Institute first became aware of how serious the pandemic would soon become, when Professor Andrew Pollard, who works for both the Jenner Institute and heads the Oxford Vaccine Group, “shared a taxi with a modeler who worked for the UK’s Scientific Advisory Group for Emergencies.” During the taxi ride, “the scientist told him data suggested there was going to be a pandemic not unlike the 1918 flu.” Due to this sole encounter, we are told, the Jenner Institute then began to pour millions into the early development of a vaccine for COVID-19 well before the scope of the crisis was clear.

For much of 2020, the Oxford-AstraZeneca vaccine was treated as an early front-runner, though its lead would later be marred by scandals related to its clinical trials, including the death of participants, sudden trial pauses, the use of a problematic “placebo” with its own host of side effects and the “unintentional” mis-dosing of some participants that skewed its self-reported efficacy rate.

The significant issues that emerged during trials have provoked little concern from the vaccine’s two lead developers, despite critical attention from even mainstream media of its complications. The lead developer of the Oxford-AstraZeneca vaccine, Adrian Hill, told NBC on December 9^th that the experimental vaccine should be approved and distributed to the public before the conclusion of the safety trials, saying,”to wait for the end of the trial would be the middle of next year. That’s too late, this vaccine is effective, available at large scale and easily deployed.”

Sarah Gilbert, the other lead researcher on the vaccine, seemed to believe that pre-mature safety approval was likely, telling the BBC on December 13 that the chances of rolling out the vaccine by the end of the year are “pretty high.” Now, the UK is expected to approve the Oxford-AstraZeneca vaccine shortly after Christmas, with India also set to approve the vaccine next week.

While the controversies surrounding the vaccine’s trials did ultimately undermine its previous frontrunner status, the Oxford-AstraZeneca vaccine remains heavily promoted as the vaccine of choice for the developing world, as it is cheaper and has much less complicated storage requirement than its main competitors, Pfizer and Moderna.

Earlier this month, Dr. Richard Horton, the editor-in-chief of the Lancet medical journal, told CNBC that “The Oxford AstraZeneca vaccine is the vaccine right now that is going to be able to immunize the planet more effectively, more rapidly than any other vaccine we have” in large part because it is a “vaccine that can get to lower middle-income countries.” CNBC also quoted Andrew Baum, global head of health care for Citi Group, as saying that the Oxford-AstraZeneca vaccine “is really the only vaccine that is going to suppress or even eradicate SARS-CoV-2, the virus that causes COVID-19, in the many millions of individuals in the developing world.”

In addition to longstanding claims that the Oxford-AstraZeneca vaccine will be the vaccine of choice for the developing world, this vaccine candidate has also been treated by several outlets in the mainstream and even independent media as “good for people, bad for profits” due to the partnership’s “explicit intention of supplying [the vaccine] around the world on a not-for-profit basis, meaning that the poorest nations on the planet will not have to worry about being shut out of a cure due to lack of funds.”

However, investigation into the vaccine’s developers and the realities of their “no-profit pledge” reveals a very different story than that which has been spun for most of the year by corporate press releases, experts and academics tied to the vaccine and the mainstream press.

For instance, mainstream media has had little, if anything, to say about the role of the vaccine developers’ private company – Vaccitech – in the Oxford-AstraZeneca partnership, a company whose main investors include former top Deutsche Bank executives, Silicon Valley behemoth Google and the UK government. All of them stand to profit from the vaccine alongside the vaccine’s two developers, Adrian Hill and Sarah Gilbert, who retain an estimated 10% stake in the company. Another overlooked point is the plan to dramatically alter the current sales model for the vaccine following the initial wave of its administration, which would see profits soar, especially if the now obvious push to make COVID-19 vaccination an annual affair for the foreseeable future is made reality.

Yet, 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 re-named UK Eugenics Society, a group notorious for its promotion of racist pseudoscience and efforts to “improve racial stock” by reducing the population of those deemed inferior for over a century.

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 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.

In the final installment of this series on Operation Warp Speed, the US government’s vaccination effort, and race, the Oxford-AstraZeneca vaccine’s ties to Eugenics-linked institutions, the secretive role of Vaccitech, and the myth of the vaccine’s sale being “non-profit” and altruistically motivated are explored in detail.

GlaxoSmithKline and the Jenner Institute

The Edward Jenner Institute for Vaccine Research was initially established in 1995 in Compton in Berkshire as a public-private partnership between the UK government, via the Medical Research Council and the Department of Health, and the pharmaceutical giant GlaxoSmithKline. Following a “review by the [institute’s] sponsors,” it was relaunched in 2005 in Oxford under the leadership of Adrian Hill, who—prior to that appointment—held a senior position at the Wellcome Trust’s Centre for Human Genetics. Hill, the lead developer of the Oxford-AstraZeneca COVID-19 vaccine, still leads a research group at Wellcome aimed at “understand[ing] the genetic basis of susceptibility to different infectious diseases, especially. . . severe respiratory infections,” which conducts most of its studies in Africa. The UK’s Medical Research Council has also become a collaborator with the Wellcome Trust, specifically on vaccine-related initiatives. The Wellcome Trust, discussed at greater length later in this article, was originally created with funding from Henry Wellcome, who founded the company that later became GlaxoSmithKline.

Hill’s partner at the Jenner Institute and the other co-developer of the Oxford COVID-19 vaccine is Sarah Gilbert. Gilbert also hails from the Wellcome Trust, where she was a “program director,” and is a student of Hill’s. Together, Gilbert and Hill have worked to position the institute to be the center of all future vaccination efforts undertaken in response to global pandemics.

Professor Sarah Gilbert at Oxford, Photo by John Cairns

The Jenner Institute’s relocation to Oxford was largely facilitated by the Medical Research Council, which donated £1.25 million between 2005 and 2006, after the decision was made to replace the institute’s original sponsors (GlaxoSmithKline, the Medical Research Council, the Department of Health) with the University of Oxford and the Institute for Animal Health, now called the Pirbright Institute. The involvement of Pirbright meant that the relaunched Jenner Institute became unique in developing vaccines for both humans and livestock.

The relaunched Jenner Institute has come to dominate publicly funded vaccine development in the UK as well as the testing of vaccines produced by the world’s largest pharmaceutical companies via clinical trials and has overseen prominent safety trials for vaccines of high media interest in recent years. Some of the Jenner Institute–conducted trials later drew controversy, such as those using South African infants in 2009 in which seven infants died.

An investigation conducted by the British Medical Journal found that the Hill-led Jenner Institute had, in the South African instance, knowingly misled parents about the negative results of and questionable methods used in animal studies as well the vaccine being known to be ineffective. The vaccine in question, an experimental tuberculosis vaccine developed jointly by Emergent Biosolutions and the Jenner Institute, was scrapped after the controversial study in infants confirmed what was already known, that the vaccine was ineffective. The trial, largely funded by Oxford and the Wellcome Trust, was subsequently praised as “historic” by the BBC. Hill, at the time the study was conducted, had a personal financial stake in the vaccine.

Similar instances of dodgy practices in efficacy trials and the effects of increased dosages have led vaccine experts to criticize the COVID-19 vaccine developed by Hill and Gilbert. Hill and Gilbert hold a considerable financial stake in the Oxford-AstraZeneca COVID-19 vaccine. While the vaccine reportedly has an efficacy of over 90 percent, those figures—often cited in mainstream reports—are self-reported by the vaccine’s developers and manufacturers (i.e., the Oxford team and AstraZeneca), which is significant given that Hill and other Jenner Institute scientists have previously been caught manipulating trial results to benefit a vaccine product in which they were personally invested.

The prominence of the Jenner Institute in vaccine development and testing has largely come through Hill’s additional leadership role at the UK’s Vaccines Network, which chooses what vaccines to develop, how to develop them, and which firms should receive “targeted investments” from the UK government. The Vaccines Network also plays a key role in identifying “what vaccine technologies could play an important role in future outbreaks.” Two of the main backers of the UK’s Vaccines Network are the Wellcome Trust and GlaxoSmithKline.

Unsurprisingly, the Vaccines Network has steered many millions of pounds toward the Hill-run Jenner Institute, with completed projects including a “plug and display” virus-like particle platform for rapid-response vaccination. Also funded by the Vaccines Network were the Jenner Institute’s initial studies of novel chimpanzee adenovirus vaccines for coronavirus (in this case, MERS), the same viral vector used for the Oxford-AstraZeneca vaccine. In addition to the Vaccines Network, the Jenner Institute also coordinates the efforts of the EU’s Vaccines Network equivalent, MultiMalVax.

Professor Adrian Hill at the Jenner Institute, Photo by John Cairns

The Jenner Institute also has a close relationship with GlaxoSmithKline and the Italian biotech Okairos, which was acquired by GlaxoSmithKline in 2014. Soon after it was acquired, Okairos, and its new owner GlaxoSmithKline, became key players in the 2014 experimental Ebola vaccine push, an effort that mirrors the current COVID-19 vaccine development rush in many key ways. The rushed safety trials for that vaccine were overseen by Adrian Hill and the Jenner Institute and funded by the UK government and the Wellcome Trust. GlaxoSmithKline and Okairos are the only firms represented on the Jenner Institute’s Scientific Advisory Board.

The Jenner Institute, along with GlaxoSmithKline-Okairos and a small French biotech called Imaxio, have been developing an experimental malaria vaccine since 2015, with human trials of that vaccine announced on December 12, 2020. Those trials will be conducted on 4,800 children in Africa over the course of 2021, in many of the same countries where Hill’s research group at the Wellcome Center for Human Genetics has been studying genetic susceptibility to several diseases. “A lot more people will die in Africa this year from malaria than will die from Covid,” Hill recently said in regard to the soon-to-begin trials.

Currently, the Jenner Institute is funded by the Jenner Vaccine Foundation, but the foundation’s documents note on several occasions a considerable influx of money from Wellcome Trust Strategic Awards. A “special review panel” from the Wellcome Trust actually lobbied the Jenner Institute to apply for further “strategic core funding” from the trust after visiting the institute and appraising its work. The Jenner Institute frames its funding from Wellcome as the key guidance behind its development decisions, which are made “based on the successful model of Wellcome Trust Strategic Award support.”

The Jenner Institute’s foundation, however, is not the only source of income for its lead researchers. Hill and Gilbert have been working to commercialize many of the institute’s vaccines through their own private company, Vaccitech. Though media reports often describe the vaccine as being a joint effort between AstraZeneca and the University of Oxford, Vaccitech is a key stakeholder in that partnership, given that the vaccine candidate relies on technology developed by Hill and Gilbert and owned by Vaccitech. A deeper look into Vaccitech offers a clue as to why the company’s name has been absent from nearly all media reports on the Oxford-AstraZeneca vaccine, as it demolishes the much-touted claim that the vaccine is “nonprofit” and offered at low cost for charitable reasons.

Vaccitech: doing well by going “good”?

The official reason Sarah Gilbert and Adrian Hill created Vaccitech in 2016 per The Times is because “Oxford’s researchers [are] encouraged to form companies to commercialize their work.” Vaccitech, like other “commercialized” Oxford research enterprises, was spun out of the Jenner Institute via the university’s commercialization arm, Oxford Science Innovations, which is currently Vaccitech’s largest stakeholder at 46 percent. Hill and Gilbert are reported to maintain a 10 percent stake in the company.

The largest investor in Oxford Science Innovations, and by extension one of the largest shareholders in Vaccitech, is Braavos Capital, the venture-capital firm started in 2019 by Andrew Crawford-Brunt, Deutsche Bank’s long-time global head of equity trading at its London branch. Through its stake in Oxford Science Innovations, Braavos owns about 9 percent of Vaccitech.

Prior to COVID-19, Vaccitech’s main focus, especially last year, was the development of a universal vaccine for the flu. Vaccitech’s efforts in this regard were praised by Google, which is also invested in Vaccitech. At the same time, the Bill & Melinda Gates Foundation was funding research to develop a universal flu vaccine, reportedly because the field of influenza vaccinology was not yet able “to design a flu vaccine that would protect broadly against the strains of flu that infect people every winter and those in nature that could emerge to trigger a disruptive and deadly pandemic,” according to a STAT News report from last year. The Gates Foundation effort originally partnered with Google’s cofounder Larry Page and his wife Lucy.

To fully finance Hill and Gilbert’s Vaccitech, and specifically its quest to develop a universal flu vaccine, Oxford Science Innovations sought £600 million from “outside investors,” chief among them the Wellcome Trust and the venture-capital arm of Google, Google Ventures. This means that Google is poised to make a profit from the Oxford-AstraZeneca vaccine at a time when its video platform YouTube has moved to ban COVID-19 vaccine–related content that shines a negative light on COVID-19 vaccines, including the Oxford-AstraZeneca candidate. Other investors in Vaccitech include Sequoia Capital’s Chinese branch and the Chinese pharmaceutical company Fosun Pharma. In addition, the UK government has put an estimated £5 million into the company and is also expected to make a return on the Oxford-AstraZeneca vaccine.

Vaccitech’s homepage showing company co-founders Adrian Hill and Sarah Gilbert. From vaccitech.co.uk

Information on the profit motive behind the Oxford-AstraZeneca vaccine has been muddied due to the extensive media promotion of the claim that Hill and Gilbert will not be collecting royalties on the vaccine and that AstraZeneca is not making a profit off the vaccine. However, this is only true until the pandemic is “officially” declared over, and the virus is labeled a persistent or seasonal condition that will require the mass administration of COVID-19 vaccines at regular intervals and possibly annually. Sky News reported that the determination of when the pandemic is over “will be based on the views of a range of [unspecified] independent bodies.” At that point, both Vaccitech and Oxford will obtain royalties from AstraZeneca’s sales of the vaccine.

Those tied to the vaccine have been at the center of promoting the idea that the COVID-19 vaccine will soon become an annual affair. For instance, in early May, John Bell—an Oxford medical professor and an “architect” of the Oxford-AstraZeneca partnership—told NBC News, “I suspect we may need to have relatively regular vaccinations against coronaviruses going into the future,” adding that the vaccine would likely be needed every year like the flu vaccine. NBC News failed to note that the Oxford-AstraZeneca vaccine in which Bell is involved stands to significantly benefit financially if that does come to pass.

More recently, Bell told The Week that, “should there prove to be a market for regular vaccinations against coronavirus in the future, ‘there is some money to be made.’” Such sentiments have been echoed by Pascal Soriot, the CEO of AstraZeneca, who told Bloomberg last month that the company stood to make a “reasonable profit” once the pandemic was declared over and COVID-19 deemed a seasonal illness requiring regular vaccinations. On this matter, Vaccitech’s CEO, Bill Enright, stated that Vaccitech investors would receive a “big chunk of the royalties from a successful vaccine as well as ‘milestone’ payments” if and when the pandemic is declared over and COVID-19 vaccines become a seasonal event.

Vaccitech, in particular, appears quite certain that this possibility is slated to become reality. For all subsequent iterations of the Oxford-AstraZeneca vaccine, Vaccitech will reacquire a much larger percentage of rights to the vaccine, rights it is currently splitting with Oxford for the first iteration. Sky News has noted that the technology that Vaccitech owns “could drive the second generation of COVID-19 vaccines” and that it “has [already] received £2.3 million of public funding to develop it.”

US government officials such as Anthony Fauci have also signaled that the COVID-19 vaccine will require annual shots. Notably, the government, through Health and Human Service’s BARDA, has poured over $1 billion into the Oxford-AstraZeneca vaccine development. In addition to government officials, several recently published mainstream media reports have claimed that the “expert” consensus “seem[s] to be leaning toward an annual shot like the flu vaccine” with regards to the COVID-19 vaccine. For instance, Dr. Charles Chiu, a professor of infectious diseases at the University of California–San Francisco, recently told Salon, “This may end up being a vaccine that’s not a one-time thing or even a two-time thing. . . it may end up being what we call either a seasonal vaccine, or vaccine that needs to be administered every couple of years.”

Such hints about an annual COVID-19 vaccine from 2021 onward have recently become commonplace from the leading COVID-19 vaccine manufacturers themselves. For instance, on December 13^th, Pfizer CEO Albert Bourla was quoted by the Telegraph as saying, “How long this [vaccine] protection lasts is something we don’t know … I think it is a likely scenario that you will need periodical vaccinations.” Pfizer also recently issued a statement that noted that “we don’t know how the virus will change, and we also don’t know how durable the protective effect of any vaccination will be,” adding that its vaccine would be suitable “for repeated administration as booster shots” in the event that the vaccine only induces an immune response for a few months.

Then, this past Tuesday, Moderna released information that suggested immunity from its COVID-19 vaccine would only last several months, with Forbes writing that “the duration of neutralizing antibodies from the Moderna vaccine will be relatively short, potentially less than a year,” an outcome that would favor the push for an annual COVID-19 shot. The developer of the Pfizer COVID-19 vaccine, Ugur Sahin of BioNTech, also stated on Tuesday that “The virus will stay with us for the next 10 years… We need to get used to the fact there’ll be more outbreaks.” He later added that “if the virus becomes more efficient… we might need a higher uptake of the vaccine for life to return to normal,” implying that these regular outbreaks he foresees occurring over the next ten years would be correlated with increased vaccine administration.

Quotes from the developers of the Oxford-AstraZeneca vaccine themselves also point to a pandemic-dominated future and a desire for the crisis to be prolonged so that the vaccine can be widely distributed. Gilbert told the UK Independent in August that she believes COVID-19 is just the beginning and that COVID-like pandemics will become more frequent in the near future. The Jenner Institute vaccine team seems so determined to create the COVID vaccine that, in June, Hill was quoted by the Washington Post in June as stating that he wanted the pandemic to stick around, saying, “We’re in the bizarre position of wanting COVID to stay, at least for a little while. But cases are declining.” He also stated that his team was in “a race against the virus disappearing.”

With the vaccine developers, “medical experts,” government officials, and the CEOs of major vaccine manufacturers all agreeing that a seasonal COVID-19 vaccine is an increasingly likely outcome, it is worth considering a possible ulterior motive regarding the initial “nonprofit” model being used by the Jenner Institute/Vaccitech and AstraZeneca for their joint COVID-19 vaccine.

Given that vaccine guidance in several countries states that each dose of the multidose COVID-19 vaccine must be produced by the same manufacturer as previous doses, the implication is that in the event of a need for periodic COVID-19 vaccine variants, those who initially received the Oxford-AstraZeneca vaccine would likely be required to receive that same “brand” of vaccine seasonally. In other words, those who initially received the Oxford-AstraZeneca vaccine would likely be required, not just to receive a second dose of the same “brand,” but continue receiving that same “brand” of vaccine every year. Notably, no interaction studies have yet been conducted on the interactions between the COVID-19 vaccines and other medications as well as other vaccines.

If this turns out to be the case, it would certainly behoove the Oxford-Vaccitech-AstraZeneca team to want their vaccine to be the most widely used one in the first year in order to guarantee the largest market for subsequent annual COVID-19 vaccines. This could be a possible motive behind the efforts of the Oxford-AstraZeneca partnership “to supply the entire world with the Oxford jab” and to supply the vaccine “to the most vulnerable groups to COVID-19.” This vaccine has already been purchased, even before regulatory approval, by governments around the world, including in Europe, North America, Australia and most Latin American countries.

The Wellcome Trust

Adrian Hill currently holds a senior position at the Wellcome Trust’s Centre for Human Genomics. The Wellcome Trust is a scientific charity based in London, established in 1936 with funds from pharmaceutical magnate Henry Wellcome. As previously mentioned, Wellcome founded the pharmaceutical company that eventually became the industry giant GlaxoSmithKline. Today, the Wellcome Trust has a $25.9 billion endowment and engages in philanthropic endeavors, including funding clinical trials and research.

Hill has been closely tied to Wellcome for decades. In 1994, he participated in the founding of the Wellcome Centre for Human Genetics and was awarded a Wellcome Trust Principal Research Fellowship the following year. He became a Wellcome professor of human genetics in 1996.

The Wellcome Centre for Human Genetics website boasts of the large-scale genetic mapping they’ve conducted in Africa. The center also publishes papers that explore genetic dispositions in relation to male fertility and “reproductive success.” The crossroads between race and genes is important in the center’s work, as an entire working group at the center, the Myers Group, is dedicated to mapping the “genetic impacts of migration events.” The center also funded a paper that argued that so long as eugenics is not coercive it’s an acceptable policy initiative. The paper asks, “Is the fact that an action or policy is a case of eugenics necessarily a reason not to do it?” According to Hill’s page on the Wellcome Trust site, race and genetics have long played a central role in his scientific approach, and his group currently focuses on the role genetics plays in African populations with regard to susceptibility to specific infectious diseases.

The Wellcome Genome Campus, which houses the Wellcome Centre for Human Genetics, is located on the grounds of Hixton Hall, in Cambridgeshire, England.

Of even greater concern, last year Science Mag reported that Wellcome was accused by both a whistleblower and the University of Cape Town South Africa of illegally exploiting hundreds of Africans by “commercializing a gene chip without proper legal agreements and without the consent of the hundreds of African people whose donated DNA was used to develop the chip.” Jantina de Vries, a bioethicist at the University of Cape Town South Africa told the journal that it was “clearly unethical.” Since the controversy, other African institutions and peoples such as the indigenous Nama peoples of Namibia have demanded that Wellcome return the DNA it collected.

The Wellcome Centre regularly co-funds the research and development of vaccines and birth control methods with the Gates Foundation, a foundation that actively and admittedly engages in population and reproductive control in Africa and South Asia by, among other things, prioritizing the wide-spread 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.

As researcher Jacob Levich wrote in the Palgrave Encyclopedia of Imperialism and Anti-Imperialism, 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.”

One example is Norplant, a contraceptive implant manufactured by Schering (now Bayer) that can prevent pregnancy for up to five years. It was taken off the US market in 2002 after more than fifty thousand women filed lawsuits against the company and the doctors who prescribed it. Seventy of those class action suits were related to side effects such as depression, extreme nausea, scalp-hair loss, ovarian cysts, migraines, and excessive bleeding.

Slightly modified and rebranded as Jadelle, the dangerous drug was promoted in Africa by the Gates Foundation in conjunction with USAID and EngenderHealth. 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.” Jadelle is not approved by the FDA for use in the United States.

Another scandal-ridden LARC is Pfizer’s Depo-Provera, an injectable contraceptive used in several African and Asian countries. The Gates Foundation and USAID have collaborated to fund this drug’s distribution and introduce it into the health-care systems of countries including Uganda, Burkina Faso, Nigeria, Niger, Senegal, Bangladesh, and India.

Andrew Pollard, director of the Oxford Vaccine Group, where Hill’s Jenner Institute resides, is enmeshed with the Gates Foundation. His employer, the University of Oxford, has received $11 million for vaccine development research from the foundation over the past three years and $208 million in grants over the past decade. In 2016, the Gates Foundation gave $36 million to a team of researchers that was headed by Pollard for vaccine development. In addition, Pollard’s private laboratory is funded by the Gates Foundation. Given this, it should come as no surprise that the Global Alliance for Vaccine Initiative (GAVI), a public-private partnership founded and currently funded by the Bill & Melinda Gates Foundation, plans to distribute the Oxford-AstraZeneca COVID-19 vaccine to low-income, predominantly African and Asian, countries once it’s approved.

The Galton Institute: Eugenics for the Twenty-First Century

Both the Wellcome Trust and Adrian Hill share a close relationship with the most infamous eugenics society in Europe, the British Eugenics Society. The Eugenics Society was renamed the Galton Institute in 1989, a name that pays homage to Sir Francis Galton, the so-called father of eugenics, a field that he often described as the “science of improving racial stock.”

In the case of the Wellcome Trust, the Trust’s library is the guardian of the Eugenics Society historical archives. When the Wellcome Trust first set up its Contemporary Medical Archive Center, the first organizational archive it sought to acquire was tellingly that of the Eugenics Society-Galton Institute. Wellcome’s website describes the Eugenics Society’s original purpose as “to increase public understanding of heredity and to influence parenthood in Britain, with the aim of biological improvement of the nation and mitigation of the burdens deemed to be imposed on society by the genetically ‘unfit’.” It also states the interests of the society’s members “ranged from the biology of heredity, a subject that developed rapidly during the first half of the 20th century, to the provision of birth control methods, artificial insemination, statistics, sex education and family allowances.” Lesley Hall, Wellcome’s senior archivist, has referred to Francis Galton, a racist eugenicist, as an “eminent late nineteenth century polymath” in her discussion of the Eugenics Society archive held at Wellcome.

A poster published by the Eugenics Society-Galton Institute in the 1930S, from the Wellcome Library

Several top governance positions at the former British Eugenics Society, now the Galton Institute, include individuals who originally worked at The Wellcome Trust, including the Galton Institute’s president Turi King. Dr. Elena Bochukova, a current Galton Council Member and Galton lecturer, previously worked under the direction of Adrian Hill at the Wellcome Trust Center for Human Genetics. The Galton Institute’s Senior Genetics Researcher, Dr. Jess Buxton, was previously a ‘genetics researcher’ at the Wellcome Trust and then went on to carry out independent research financed by Wellcome. Her research, which is particularly race oriented, includes creating the first genetic sequence map of a native Nigerian. Moreover, Adrian Hill himself spoke at the Eugenics Society-Galton Institute at the celebration of their 100th anniversary in 2008.

The Galton Institute publishes what they now call the Galton Review, previously titled the Eugenics Review, where various members of the self-proclaimed “learned society” publish papers focused on population issues, genetics, evolutionary biology, and fertility.

A look at early issues of the Eugenics Review shines a light on Galton’s original ambitions. In the 1955 issue titled “The Immigration of Colored People,” an author asks, “What will become of our national character, good workmanship etc. in the course of a few decades if this immigration of negroes and negroids continues unchecked?” The article ends with an appeal to readers to write their parliamentary representatives and urge them that in view of “racial betterment or deterioration” something must be done urgently to “check the present influx of africans and other negroids.”

Today, it appears that the Galton Institute continues to see the immigration of racial minorities into European cities as an unchecked threat. Mike Coleman, an Oxford professor of demographics and a fellow at the institute runs an anti-immigration organization and advocacy group called MigrationWatch—whose mission is to preserve the European culture of the UK by lobbying the government to stem legal immigration and publishing data that supposedly demonstrates the biological and cultural threat of increasing immigration.

A 1961 issue of the Eugenics Review titled “The Impending Crisis” claims the function of the institute’s upcoming conference is “to honor Margaret Sanger” and describes the population crisis as “quantity threatening quality.”

Sanger, known as the “pioneer of the American birth control movement,” was a staunch advocate for promoting “racial betterment” and the key architect of the Negro Project, which she claimed “was established for the benefit of the colored people.” But as medical ethics fellow at Harvard Medical School, Harriet Washington, argues in her book Medical Apartheid, “The Negro Project sought to find the best way to reduce the black population by promoting eugenic principals.” Sanger was an American member of the British Eugenics Society.

Another early member of the Galton Institute was John Harvey Kellogg, prominent business man and eugenicist. Kellogg founded the Race Betterment Foundation and argued that immigrants and nonwhites would damage the American gene pool. Yet another example is Charles Davenport, a scientist known for his collaborative research efforts with eugenicists in Nazi Germany and his contributions to Nazi Germany’s brutal racial policies, who was vice president of the Galton Institute in 1931.

Another more recent member of the Galton Institute was David Weatherall, for whom the Weatherall Institute of Molecular Medicine at Oxford is named. Weatherall was a member of the Galton Institute when it was still named the Eugenics Society and he remained a member until his death in 2018. Weatherall, who was knighted by the British monarch in 1987 for his contributions to science, addressed the Galton Institute on numerous occasions and gave a senior lecture on genetics at the institute in 2014, of which no transcript or video is available. As an Oxford professor, Weatherall was Adrian Hill’s doctoral adviser and eventually his boss when Hill began working at the Weatherall Institute conducting immunogenic research in Africa. A key fixture of the Weatherall Institute of Molecular Medicine since its founding is Walter Bodmer, a former president of the Galton Institute.

While the Galton Institute has attempted to distance itself from its past of promoting racial eugenics with surface-level public relations efforts, it has not stopped family members of the infamous racist from achieving leadership positions at the institute. 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, originally dreamt up by Galton’s former president Walter Bodmer, 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.”

Who gets the safest vaccines?

Considering the degree to which the players and institutions behind the Oxford-AstraZeneca vaccine (including the lead developer) are tied and connected to institutions that have been instrumental in the rise and perpetuation of racial eugenics, it’s concerning that this particular vaccine is being portrayed by scientists and media alike as the COVID-19 vaccine for the poor and the Global South.

The Oxford-AstraZeneca vaccine sells at a fraction of the cost of its COVID-19 vaccine competitors—running between 3 and 5 dollars per dose. Moderna and Pfizer cost 25 to 37 dollars and 20 dollars per dose, respectively. As CNN recently reported, the Oxford-AstraZeneca vaccine will “be far easier to transport and distribute in developing countries than its rivals,” several of which require complicated and costly cold supply chains. When the Thomson Reuters Foundation asked several experts which COVID-19 vaccine could “reach the poorest soonest,” all declared a preference for the Oxford-AstraZeneca candidate.

There is also the added fact that a host of safety issues have come to surround the vaccine. Recently, on November 21, a forty-year-old participant in AstraZeneca’s clinical trial who lives in India sent a legal notice to the Serum Institute of India alleging that the vaccine caused him to develop acute neuroencephalopathy, or brain damage. In the notice, the participant said he “must be compensated, in the least, for all the sufferings that he and his family have undergone and are likely to undergo in the future.”

In response, the Serum Institute claimed the participant’s medical complications are unrelated to the vaccine trial and said it would take “legal action” against the brain-damaged participant for maligning the company’s reputation, seeking damages in excess of $13 million. “This is the first time I have ever heard of a sponsor threatening a trial participant,” Amar Jesani, editor of the Indian Journal of Medical Ethics, said of the incident. The Serum Institute has received at least $18.6 million from the Bill & Melinda Gates Foundation and has a deal with AstraZeneca to manufacture a billion doses of the vaccine.

Other manufacturers chosen by Oxford-AstraZeneca to produce their vaccine are also no strangers to controversy. For instance, their manufacturing partner in China, Shenzhen Kangtai Biological Products, has been at the center of controversy for years, especially after 17 infants died from its Hepatitis B vaccine in 2013. The New York Times cited Yanzhong Huang, a senior fellow for global health at the Council on Foreign Relations, as saying: “Imagine if a similar scandal is reported again in China… It’s not just going to undermine the confidence of the company manufacturing the vaccine, it’s also going to hurt the reputation of AstraZeneca itself and their vaccine, too.”

In another example, the manufacturing partner chosen to produce the vaccine in the US is the scandal-ridden company with ties to the 2001 anthrax attacks, Emergent Biosolutions. Emergent Biosolutions, previously known as BioPort, has a long track record of knowingly selling and marketing products that were never tested for safety and efficacy, including its anthrax vaccine BioThrax and its biodefense product Trobigard. The current head of quality control for Emergent Biosolutions’ lead manufacturing facility in the US has no expertise in pharmaceutical manufacturing and is instead a former high-ranking military intelligence official who operated in Iraq, Afghanistan and beyond.

The issues raised by their decision to partner with manufacturers with dark histories of product safety issues are compounded by the adverse reactions reported in the Oxford-AstraZeneca trials as well as the ways in which those trials have been conducted. In September, AstraZeneca was forced to pause its experimental COVID-19 vaccine trial after a woman in the UK developed a “suspected serious reaction” that the New York Times reported was consistent with transverse myelitis. TM is a neurological disorder characterized by inflammation of the spinal cord, a major element of the central nervous system. It often results in weakness of the limbs, problems emptying the bladder, and paralysis. Patients can become severely disabled, and there is currently no effective cure.

Concern over an association between TM and vaccines is well established. A review of published case studies in 2009 documented thirty-seven cases of TM associated with various vaccines, including hepatitis B, measles-mumps-rubella, diphtheria, pertussis, tetanus, among others in infants, children, and adults. The researchers in Israel noted, “The associations of different vaccines with a single autoimmune phenomenon allude to the idea that a common denominator of these vaccines, such as an adjuvant, might trigger this syndrome.” Even the New York Times article on the AstraZeneca trial pause notes past “speculation” that vaccines might be able to trigger TM.

In July, an Oxford-AstraZeneca trial participant developed symptoms of TM, and the vaccine trial was paused at that time. An “independent panel” ultimately concluded the illness was unrelated to the vaccine, and the trial continued. Yet, as Nikolai Petrovsky from Flinders University told the Australian Broadcasting Corporation, these panels are typically made up of “biostatisticians and also medical representatives from the sponsor drug company running the trial.” Then, in October, a trial participant in Brazil died, though in that case, AstraZeneca suggested that the person was part of the control group and thus hadn’t received the COVID-19 vaccine.

According to Forbes, the AstraZeneca vaccine was ineffective at stopping the spread of coronavirus in their animal trials. All six monkeys injected with AstraZeneca’s COVID-19 vaccine became infected with the disease after being inoculated. All the monkeys were put to death, which means that it will remain unknown whether those monkeys would have suffered other adverse effects.

Another concern is that trial administrators gave the trial control group (for both human and animal trials) Pfizer’s Nimenrix, a meningitis vaccine, as opposed to a saline solution, which is regarded as the gold standard for controls because researchers can be sure the saline solution won’t cause any adverse reactions. Using Pfizer’s meningitis vaccine as the control placebo allows AstraZeneca to downplay any adverse reactions in its COVID-19 vaccine group by showing that the control group suffered adverse reactions as well. “The meningitis vaccine in the AstraZeneca trial is what I would call a ‘fauxcebo,’ a fake control whose real purpose is to disguise or hide injury in the vaccine group,” said Mary Holland, general counsel at Children’s Health Defense.

Eugenics under another name

Despite these safety concerns and clinical trial scandals, close to 160 countries have purchased the Oxford-AstraZeneca vaccine, and now reports are suggesting that India, the country with the second largest population on Earth, is likely to approve this vaccine by next week.

As documented here, while the vaccine may be heralded as “vital for lower-income countries,” the Oxford-AstraZeneca project is no mere philanthropic pursuit. Not only is there a significant profit motive behind the vaccine, but its lead researcher’s connection to the British Eugenics Society adds another level of warranted scrutiny.

For those encountering stories of eugenicists, it’s common to dismiss such activity as that of “conspiracy theories.” However, it’s undeniable that several prominent individuals and institutions that remain active today have clear ties to eugenicist thinking, which was not so taboo just a few decades ago. Unfortunately, this holds true for the individuals and institutions associated with the Oxford-AstraZeneca COVID vaccine, who, as demonstrated in this article, immerse themselves in studies of race science and population control – primarily in Africa while working closely with institutions that have direct and longstanding links to the worst of the Eugenics movement.

As this series has shown, there are many concerns regarding the points where race and the COVID-19 vaccination campaign in the US and abroad intersect, both publicly and privately. Part I of this series raised questions about the policy-shaping role of the Johns Hopkins Center for Health Security, which suggested that the US government make COVID-19 vaccines available to ethnic minorities and the mentally challenged first. Part II explained how in order to allocate COVID-19 vaccines in the US, health agencies are using a program created by Palantir, a company with a record of helping the US agencies target ethnic minorities through immigration policy and racist policing.

Furthermore, there are plans in place to exercise what could reasonably be described as economic coercion to pressure people to “voluntarily” get vaccinated. Such coercion will be obviously be more effective on poor and working communities, meaning communities of color will be disproportionately affected as well.

Considering these facts, and the case for scrutinizing the safety of Oxford-AstraZeneca’s “affordable” vaccine option made above, any harm caused by vaccine allocation policy in the US and beyond is likely to disproportionately affect poor communities, especially communities of color.

As such, the public should take all vaccine rollout policy with a grain of salt, even when they come cloaked in language of inclusion, racial justice, and public health preservation. As the co-founder of the American Eugenics Society (later renamed “Society for the Study of Social Biology”) Frederick Osborn put it in 1968, “Eugenic goals are most likely to be attained under a name other than eugenics.”

December 26, 2020 Posted by aletho | Deception, Ethnic Cleansing, Racism, Zionism, Science and Pseudo-Science, Supremacism, Social Darwinism | COVID-19 Vaccine, UK | Leave a comment

Pfizer COVID jab warning: No breastfeeding, avoid pregnancy for 2 months, unknown fertility impacts

By Dorothy Cummings McLean – LifeSiteNews – December 4, 2020

WESTMINSTER, England — Government produced safety instructions for a new coronavirus vaccine indicate that it should not be used by pregnant or breast-feeding mothers and children. In addition, they state that it is unknown what effect the COVID-19 mRNA vaccine will have on fertility.

The ten-page “Reg 174 Information for UK Healthcare Professionals” describes the vaccine, how it is to be stored, diluted, and administered, and the trial studies carried out to test it. To be effective, the vaccine is supposed to be administered twice. In a section called “Fertility, pregnancy and lactation,” the guide says there is “no or limited data” on the vaccine. Therefore, it is not recommending its use for pregnant women.

“Animal reproductive toxicity studies have not been completed. COVID-19 mRNA Vaccine BNT162b2 is not recommended during pregnancy,” the guide states in section 4.6. “For women of childbearing age, pregnancy should be excluded before vaccination.”

The guide also advises that women should avoid becoming pregnant for the first two months after their Covid-19 shots.

“In addition, women of childbearing age should be advised to avoid pregnancy for at least 2 months after their second dose,” it says.

Because it is still unknown whether or not the vaccine can be transmitted to a breast-feeding infant through his or her mother’s milk, the instructions state that “a risk to the newborns/infants cannot be excluded.” Therefore, the guide specifies that the vaccine “should not be used during breast-feeding.”

But alarmingly the guide has only one thing to say about the vaccine’s impact on fertility: they don’t know if it does or doesn’t.

“It is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility,” it states.

The guide notes that the safety of the vaccine was tested in two clinical studies. The first study enrolled 60 people aged 16 to 55, and the second involved “approximately” 44,000 people aged 12 and older. The most common negative effects of the vaccine in people over the age of 16 have been “pain at the injection site” (a muscle), experienced by over 80%, fatigue (over 60%), headache (over 50%), sore muscles (over 30%), chills (over 30%), joint pain (over 20%), and fever (over 10%). According to the guide, these side-effects “were usually mild or moderate in intensity” and went away after a few days.

Fertility fears

Earlier this week, two leading doctors wrote to the European Medicine Agency, which is responsible for the safety of vaccines, in an attempt to stop human trials of all Covid-19 vaccines, especially the Pfizer/BioNtech COVID-19 mRNA Vaccine BNT162b2 described above. Dr. Michael Yeadon, a former head of Pfizer’s respiratory research, and Dr. Wolfgang Wodarg, a health policy advisor, think that human testing is still unethical.

Among other concerns, Yeadon and Wodart warn that some of the vaccines may prevent the safe development of placentas in pregnant women, resulting in “vaccinated women essentially becoming infertile.”

“Several vaccine candidates are expected to induce the formation of humoral antibodies against spike proteins of SARS-CoV-2,” the doctors wrote.

“Syncytin-1 […] which is derived from human endogenous retroviruses (HERV) and is responsible for the development of a placenta in mammals and humans and is therefore an essential prerequisite for a successful pregnancy, is also found in homologous form in the spike proteins of SARS viruses,” they continued.

“There is no indication whether antibodies against spike proteins of SARS viruses would also act like anti-Syncytin-1 antibodies. However, if this were to be the case this would then also prevent the formation of a placenta which would result in vaccinated women essentially becoming infertile.”

The doctors suggest that because the Pfizer/BioNTech trial protocol says that “women of child-bearing potential” can take part only if they are not pregnant or breastfeeding and are using contraception, it could take “a relatively long time before a noticeable number of cases of post-vaccination infertility could be observed.”

Pfizer can’t be sued for damages

According to the U.K.’s Independent newspaper, Pfizer, the owner of the COVID-19 mRNA Vaccine BNT162b2 has been given indemnity in the United Kingdom, which means that people who suffer damage from the vaccine will not be able to sue the company.

“NHS (National Health Service) staff providing the vaccine, as well as manufactures of the drug, are also protected,” the Independent reported.

The newspaper also reported that the Pfizer/BioNTech vaccine was authorised by the Medicines and Healthcare products Regulatory Agency on Tuesday under Section 174 of the Human Medicine Regulations 2012.

The regulation, which was altered by the British government this autumn, currently states that the ordinary “prohibitions” in Britain’s requirements for authorization “do not apply where the sale or supply of a medicinal product is authorized by the licensing authority on a temporary basis in response to the suspected or confirmed spread of— (a) pathogenic agents; (b) toxins; (c ) chemical agents; or (d) nuclear radiation, which may cause harm to human beings.”

The Independent noted that in a press conference on Wednesday, Pfizer’s U.K. managing director refused to explain why the company needed this legal protection.

“We’re not actually disclosing any of the details around any of the aspects of that agreement and specifically around the liability clauses,” said Pfizer’s Ben Osborn.

Curiously, in October the government’s Medicines & Healthcare products Regulatory Agency (MHRA), posted a bid request stating that “For reasons of extreme urgency,” they seek “an Artificial Intelligence (AI) software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reaction (ADRs).” The bid goes on to explain that “it is not possible to retrofit the MHRA’s legacy systems to handle the volume of ADRs that will be generated by a Covid-19 vaccine,” and that this “represents a direct threat to patient life and public health.”

December 25, 2020 Posted by aletho | Timeless or most popular | COVID-19 Vaccine | Leave a comment

Fauci admits to LYING about Covid-19 herd immunity threshold to manipulate public support for vaccine

RT | December 25, 2020

Dr. Anthony Fauci, the epidemiologist revered almost religiously as a hero by mainstream media outlets and Democrat politicians, has admitted that he lied to Americans to manipulate their acceptance of a new Covid-19 vaccine.

The intentional deception involved estimates for what percentage of the population will need to be immunized to achieve herd immunity against Covid-19 and enable a return to normalcy.

Earlier this year, Fauci said 60-70 percent – a typical range for such a virus – but he moved the goalposts to 70-75 percent in television interviews about a month ago. Last week, he told CNBC that the magic number would be around “75, 80, 85 percent.”

When pressed on the moving target in a New York Times interview, Fauci said he purposely revised his estimates gradually. The newspaper, which posted the article on Thursday, said Fauci changed his answers partly based on “science” and partly on his hunch “that the country is finally ready to hear what he really thinks.”

“When polls said only about half of all Americans would take a vaccine, I was saying herd immunity would take 70 to 75 percent,” Fauci said. “Then, when newer surveys said 60 percent or more would take it, I thought, ‘I can nudge this up a bit,’ so I went to 80, 85.”

Fauci added that he doesn’t know the real number but believes the range is 70-90 percent. He said it may take nearly 90 percent, but he won’t give that number because Americans might be discouraged, knowing that voluntary acceptance won’t be high enough to reach that goal.

The article was published on Fauci’s 80th birthday, which was celebrated in the nation’s capital as “Dr. Anthony Fauci Day” after being proclaimed as such by Washington’s Democrat mayor, Muriel Bowser. CNN and other media outlets covered the occasion glowingly, including Fauci being surprised with a “serenade” by emergency medical workers as he left his office at the National Institutes of Health on Wednesday. A CNN video of the serenade included an audio clip of President-elect Joe Biden and his wife, Jill Biden, singing the birthday song.

You have been a beacon of scientific thinking and enlightenment during “these dark ages” of ignorance and superstition. Thank you!

— Mehmet Guvendi (@guvendi_mehmet) December 24, 2020

But the doctor’s changing story on herd immunity is only the latest in a series of Covid-19 flip-flops, including 180-degree shifts on such core issues as whether members of the general public should wear masks and whether children should be sent back to school.

Just as his tone on herd immunity changed, his view on prospects for a return to normalcy shifted dramatically. A few days before the November 3 presidential election, he echoed Biden’s gloomy Covid-19 outlook and implied that the Democrat challenger would deal with the crisis more seriously than would President Donald Trump. After the election, he turned far more optimistic.

Of course he does, remember when he said face masks don’t work and he doesn’t recommend them, then now he says they do and are essential? The fact that people still listen to these experts is the most worrying thing.

— Dan Mitchell (@theantifitPT) December 24, 2020

“This is not the first time that Fauci has admitted to deceiving the public for utilitarian purposes in regard to coronavirus,” journalist Ari Hoffman tweeted. Another observer agreed, pointing out Fauci’s flip-flop on masks. “The fact that people still listen to these experts is the most worrying thing,” he said.

Setting expectations for getting economic activity back to normal is virtually impossible without realistic projections for the vaccination rate that would provide herd immunity. Dr. Moncef Slaoui, chief scientific adviser for the Trump administration’s vaccine rollout, said in late November that “true herd immunity” would take place without about 70 percent of Americans inoculated, which might be achieved by sometime in May 2021.

Fauci’s admitted Covid-19 deception is symptomatic of how government officials “infantilize the American people,” one commenter said. “We’re going to be in trouble when we don’t have Trump to blame everything on and people have to find a way to cope.”

But the doctor remains a superstar in the minds of many Americans, with some Twitter users calling him a “beacon of scientific thinking and enlightenment during these dark ages of ignorance and superstition.”

Radio host John Ziegler offered a theory as to how Trump got the blame for 326,000 US Covid-19 deaths, while following Fauci’s policy advice, while the doctor was elevated by the media as a hero and genius. “Fauci is really loved because it is perceived he took down Trump, not Covid,” Ziegler said.

The most insane COVID media narrative… Dr. Fauci is a hero/genius.But the USA response he led was a disaster.And Trump, who did everything Fauci told him, is responsible for over 300,000 deaths!Fauci is REALLY loved because it is perceived he took down Trump, not COVID!

— John Ziegler (@Zigmanfreud) December 24, 2020

December 25, 2020 Posted by aletho | Deception, Science and Pseudo-Science, Timeless or most popular | Covid-19, COVID-19 Vaccine, United States | Leave a comment

THE TRAIL OF TRUTH

SixthSense | December 23, 2020

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December 24, 2020 Posted by aletho | Civil Liberties, Deception, Science and Pseudo-Science, Timeless or most popular, Video | Covid-19, COVID-19 Vaccine, Human rights, UK | Leave a comment

Vicious criminal Neil Ferguson playing key role in new lockdowns

By Jon Rappoport | No More Fake News | December 24, 2020

Let me boil this down for you. Claiming a new “mutant strain” of SARS-CoV-2 is 70% more deadly than the original, computer modelers in the UK have advised Prime Minister, Boris Johnson, to lock down the country at a much stricter level.

The computer model was concocted at the Imperial College of London. The accompanying text actually admits it’s too early to tell whether the mutant strain is a major threat.

Nevertheless, Boris Johnson has issued the new vast lockdown order. [1] [2]

Who is on television promoting the need for the lockdown? None other than Neil Ferguson, the disgraced and failed computer modeler. [3] [4]

He didn’t author the new model/study at the Imperial College, but he’s now the face of the “science.”

Ferguson’s prior model predicted 500,000 COVID deaths in the UK and 2 million in the US would occur by last summer. This absurd and criminal estimate directly influenced Boris Johnson and Donald Trump to declare states of emergency, and abandon plans to keep their national economies open.

Then Ferguson violated his own lockdown recommendations by carrying on an affair with his mistress, who lived in her separate home with her husband.

And now he’s back, on television, warning citizens about the new “mutant strain” of the virus and the need for a higher level of lockdown.

Other scientists are outraged at the latest computer model; they are demanding to see the actual evidence of the increased threat. They’re saying they don’t even understand what “70% more deadly than the original strain” means.

How much more economic devastation can the people of the UK take?

Here is my original piece on Neil Ferguson, written as his prior computer model was being trashed—but followed by political leaders in the US, UK, France, and Germany. Buckle up:

Neil Ferguson: the ghost in the machine [5]

Why do governments salute when he predicts a pandemic and tells them to lock down their countries?

Does anyone care about his past?

Why does he still have a prestigious job?

Who is he connected to?

by Jon Rappoport

Neil Ferguson, through his institute at London’s Imperial College, can call the shots on a major percentage of the global population.

He’s Mr. Genius, when it comes to projecting computer models of epidemics.

Fellow experts puff up his reputation.

According to the Business Insider (4/25) [6], “Ferguson’s team warned Boris Johnson that the quest for ‘herd immunity’ [letting people live their lives out in the open in the UK] could cost 510,000 lives, prompting an abrupt U-turn [massive national lockdown in the UK]… His simulations have been influential in other countries as well, cited by authorities in the US, Germany, and France.”

Not only cited, not only influential, but swallowed whole.

Business Insider continues: “On March 23, the UK scrapped ‘herd immunity’ in favor of a suppression strategy, and the country made preparations for weeks of lockdown. Ferguson’s study was responsible.”

There’s more. A lot more.

Same Business Insider article: “Dr Deborah Birx, coronavirus response coordinator to the Trump administration, told journalists at a March 16 press briefing that the Imperial paper [Ferguson’s computer projection] prompted the CDC’s new advice to work from home and avoid gatherings of 10 or more.”

Ferguson, instigator of LOCKDOWN. Stripping away of basic liberties. Economic devastation.

So let’s look at Ferguson’s track record, spelled out in the Business Insider piece:

“Ferguson co-founded the MRC Centre for Global Infectious Disease Analysis, based at Imperial, in 2008. It is the leading body advising national governments on pathogen outbreaks.”

“It gets tens of millions of dollars in annual funding from the Bill & Melinda Gates Foundation, and works with the UK National Health Service, the US Centres for Disease Prevention and Control (CDC), and is tasked with supplying the World Health Organization with ‘rapid analysis of urgent infectious disease problems’.”

Getting the picture?

Gates money goes to Ferguson.

Ferguson predicts dire threat from COVID, necessitating lockdowns—thus preparing people to accept a vaccine. The vaccine Gates wants.

Ferguson supplies a frightening computer projection of COVID deaths—to the CDC and WHO. Ferguson thus communicates a rationale for the Gates vaccine plan.

National governments surrender to WHO and CDC. LOCKDOWNS.

Business Insider : “Michael Thrusfield, a professor of veterinary epidemiology at Edinburgh University, told the paper he had ‘déjà vu’ after reading the [Ferguson] Imperial paper [on COVID], saying Ferguson was responsible for excessive animal culling during the 2001 Foot and Mouth [mad cow] outbreak.”

“Ferguson warned the government that 150,000 people could die. Six million animals were slaughtered as a precaution, costing the country billions in farming revenue. In the end, 200 people died.”

“Similarly, he [Ferguson] was accused of creating panic by overestimating the potential death toll during the 2005 Bird Flu outbreak. Ferguson estimated 200 million could die. The real number was in the low hundreds.” HELLO?

“In 2009, one of Ferguson’s models predicted 65,000 people could die from the Swine Flu outbreak in the UK — the final figure was below 500.”

So you have to ask yourself, why would anyone believe what Ferguson has been predicting in this COVID hustle?

Are his fellow experts that stupid?

Are presidents and prime ministers that stupid?

And the answer is: This is a monumental covert op; some people are that stupid; some are caught up in the op and are afraid to say the emperor has no clothes; some are aware of what is going on, and they want to destroy national economies and lead us into, yes, a new world order.

Gates knows he has his man: Ferguson. As the recipient of tens of millions of dollars a year from the Gates Foundation, Ferguson isn’t about to issue a model that states: COVID is nothing to worry about, let people live their lives and we’ll be all right. The chance of that happening is on a par with researchers admitting they never properly identified a new virus as the cause of illness in 2019, in Wuhan. [7]

In order to justify injecting every man, woman, and child in the world with heavy metals, synthetic genes that alter genetic makeup, a host of germs, and who knows what else, Gates needs A STORY ABOUT A DEADLY VIRUS THAT NECESSITATES SHUTTING DOWN AND IMPRISONING THE PLANET, ACHIEVING A CAPTIVE AUDIENCE.

He’s got the story, all dressed up in a computer model, composed by a man with a past record of abject and devastating failures.

Neil Ferguson is the ghost in the machine. The machine is the World Health Organization and the CDC. The man behind the ghost is Bill Gates.

SOURCES:

[1] https://www.thesun.co.uk/news/13524419/new-covid-strain-london-cases-double/

[2] https://www.thelastamericanvagabond.com/flawed-data-model-from-imperial-college-blame-for-latest-uk-lockdown/

[3] https://www.dailymail.co.uk/news/article-9074765/Professor-Lockdown-Neil-Ferguson-warns-Tier-Four-needed-Easter.html

[4] https://www.dailymail.co.uk/news/article-9073767/Professor-Neil-Ferguson-key-role-Boris-Johnsons-dramatic-U-turn-Christmas.html

[5] https://blog.nomorefakenews.com/2020/04/30/the-british-corona-middle-man/

[6] https://www.businessinsider.com/neil-ferguson-transformed-uk-covid-response-oxford-challenge-imperial-model-2020-4

[7] https://blog.nomorefakenews.com/2020/04/29/covid-two-vital-experiments-have-never-been-done/

December 24, 2020 Posted by aletho | Deception, Science and Pseudo-Science, Timeless or most popular | Covid-19, COVID-19 Vaccine, France, UK, United States, WHO | Leave a comment

France Forced To POSTPONE ‘Health Dictatorship’ Vaccine Legislation

Massive backlash against “vaccine blackmail” means delay in proposed legislation

By Steve Watson | Summit News | December 24, 2020

A radical bill proposed by the French Government that would see unvaccinated people refused basic services such as public transport has been put on ice after a massive backlash.

The proposed law mandates that citizens have proof of a negative COVID test or “preventative treatment, including the administration of a vaccine” in order to “access transport or to some locations, as well as certain activities.”

However, the government has been forced to delay the legislation after angry protests.

French Health Minister Olivier Véran publicly postponed the bill in an announcement Tuesday evening.

“Because there needs to be trust for the French people to go and get vaccinated of their own free will, because we’re still in a state of sanitary crisis … the government won’t present the text [to the National Assembly] for several months, before we’re out of the crisis,” Véran stated.

The bill was lambasted by political figures across the spectrum, with conservative MP Fabien Di Filippo labelling it “vaccine blackmail.”

RN leader Marine Le Pen branded the vaccine measure “essentially totalitarian.”

“In a backhanded way, this bill does not aim to make vaccinations mandatory, but will prevent anybody who doesn’t comply from having a social life,” she said.

RN party spokesman Sebastien Chenu called the plan a “health dictatorship,” while centrist senator Nathalie Goulet said the draft was “an attack on public freedoms.”

Guillaume Peltier, deputy leader of the center-right LR party, warned that the law would allow the government to “get all the power to suspend our freedoms without parliamentary control.”

France’s vaccination program, set to get underway on Sunday, will not be mandatory, but a majority of 55% of citizens say they will not get the shot.

As we previously highlighted, France has imposed some of the strictest lockdown measures in Europe, with citizens having to fill out a form every time they leave their home.

December 24, 2020 Posted by aletho | Civil Liberties | COVID-19 Vaccine, France, Human rights | Leave a comment

The Future of Vaccines

Corbett • 12/23/2020

Podcast: Play in new window | Download | Embed

If the Gateses and the Faucis and the representatives of the international medical establishment get their way, life will not return to normal until the entire planet is vaccinated against SARS-CoV-2. What many do not yet understand, however, is that the vaccines that are being developed for SARS-Cov-2 are unlike any vaccines that have ever been used on the human population before. And, as radically different as these vaccines appear, they represent only the very beginning of a complete transformation of vaccine technology that is currently taking place in research labs across the planet. This is a study of The Future of Vaccines.

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TRANSCRIPT

Since the dawn of the corona crisis, we have been told over and over that the world has changed forever.

MARIA VAN KERKHOVE: What we’re going to have to figure out, and I think what we’re all going to have to figure out together, is what our new normal looks like. Our new normal includes physical distancing from others. Our new normal includes wearing masks where appropriate. Our new normal includes us knowing where this virus is each and every day, where we live, where we work, where we want to travel.

SOURCE: What the New Normal Looks Like After Covid-19

DUCEY: What we’ve gone through and the challenges that I’m sharing with you really is Arizona’s new normal. And it’s our new normal for the foreseeable future. I really want ask people to get their heads around that.

SOURCE: Arizona Gov. Ducey Holds Coronavirus Briefing

JUSTIN TRUDEAU: This pandemic has provided an opportunity for a reset. This is our chance to accelerate our pre-pandemic efforts to reimagine economic systems that actually address global challenges like extreme poverty, inequality and climate change.

SOURCE: Coronavirus: Trudeau tells UN conference that pandemic provided “opportunity for a reset”

This “New Normal” with which we are being threatened brings with it great uncertainty. Uncertainty over work. Uncertainty over travel. Uncertainty over what our lives will look like on the other side of this “Great Reset.”

But there is one thing that we can be certain about: If the Gateses and the Faucis and the representatives of the international medical establishment get their way, life will not return to normal until the entire planet is vaccinated against SARS-CoV-2.

GATES: It is fair to say things won’t go back to truly normal until we have a vaccine that we’ve gotten out to basically the entire world.

SOURCE: Bill Gates on his 2015 ‘virus’ warning, efforts to fight coronavirus pandemic

ZEKE EMANUEL: Realistically, COVID-19 will be here for the next 18 months or more. We will not be able to return to normalcy until we find a vaccine or effective medications.

SOURCE: Dr. Zeke Emanuel On The Return To ‘Normal’

DOUG FORD: The hard fact is, until we find a vaccine, going back to normal means putting lives at risk.

SOURCE: Ontario announces $20 million for COVID-19 vaccine research

JUSTIN TRUDEAU: This will be the new normal until a vaccine is developed.

SOURCE: PM Trudeau on modelling data and federal response to COVID-19 – April 9, 2020

GAVIN NEWSOM: As I said: normal it will not be, at least until we have herd immunity and we have a vaccine.

SOURCE: California Gov. Newsom Holds Coronavirus Briefing

ANTHONY FAUCI: So, if we get the overwhelming majority of people taking the vaccine, and you have, on the one hand, an effective vaccine, on the other hand, a high degree of uptake of the vaccine, we could start getting things back to relative normal as we get into the second and third quarter of the year, where people can start thinking about doing things that were too dangerous just months ago.

SOURCE: Fauci: We’ll Get Back to Normal Gradually After Vaccine; You Don’t Know How Effective Vaccine Is for You

NORMAN SWAN: The only thing that will really allow life as we once knew it to resume is a vaccine.

SOURCE: Life will only return to normal when there’s a coronavirus vaccine, Dr Norman Swan says

This message has been repeated so frequently and so consistently by public health officials, political “leaders” and media commentators that many have begun to believe it. And now, the public is being prepared for an unprecedented global vaccination campaign. Taking the form of a military operation . . .

GENERAL GUSTAVE PERNA: It is this effort that I can look you in the face and say to you, “E.U.A. [Emergency Use Authorization] comes, 24 hours later vaccines will be distributed out to the American people and be ready for administration.”

SOURCE: General Perna says vaccine distribution will begin 24 hours after Emergency Use Authorization

. . .the plan is to rush a new generation of experimental vaccines to market and deliver them at “warp speed” before any long term testing has even been attempted. What many do not yet understand, however, is that the vaccines that are being developed for SARS-Cov-2 are unlike any vaccines that have ever been used on the human population before.

And, as radically different as these vaccines appear, they represent only the very beginning of a complete transformation of vaccine technology that is currently taking place in research labs across the planet.

This is a study of The Future of Vaccines.

You’re tuned in to The Corbett Report.

For almost the entirety of 2020, a traumatized public has been told that nothing resembling our pre-corona lives will return until there is a COVID vaccine.

So it is no surprise that the same media sources that have been promoting this talking point would celebrate the hopeful pronouncements of the Big Pharma manufacturers regarding their COVID vaccine candidates.

BECKY QUICK: Welcome back to Squawk Box everybody. We have some breaking news from Pfizer. Meg Tirrell joins us right now. Meg, good morning.

MEG TIRELL: Good morning, Becky. This is the news that we’ve been waiting to hear.
Pfizer and BioNTech reporting the first results from their phase 3 vaccine trial saying that in this interim look the vaccine showed to be more than 90 percent effective.

SOURCE: Pfizer, BioNTech announce Covid-19 vaccine candidate is 90% effective

JAKE WHITTENBERG: Well, we begin with breaking news this morning. The push to find a coronavirus vaccine. This morning, Moderna says its vaccine is more than 94 percent effective.

SOURCE: BREAKING: Moderna coronavirus vaccine “more than 94% effective”

TIM STENOVEC: Vaccine headlines are rolling in. One of AstraZeneca’s doses stopped an average of 70 percent of patients from falling ill and that even rose to 90 percent with additional regimens now the head of the government’s operation warp speed is saying that quote hopefully vaccinations in the u.s will start in less than three weeks.

SOURCE: AstraZeneca-Oxford Vaccine Found Effective in Preventing Covid

But lost amid the hype of this media-led celebration are some sobering facts.

Firstly, these news stories were not generated on the back of publicly accessible data, but literal corporate press releases. This announcement-by-press-release style of corporate self-reporting was immediately exposed as a sham when AstraZeneca was found to have given an “unintentionally” lower dose to one group of trial participants and then touted the results of that smaller dose group without clarifying the confusion.

FRANCINE LACQUA: I’m not really sure what to make of this AstraZeneca-Oxford trial there’s confusion about whether it’s 60 efficacy whether it’s 90 what exactly happened.

ANDREW PEKOSZ: Well it is a little bit unclear, but let’s start with what we think we know. which is some of the patients that were in their phase three clinical trial ended up getting a half-dose of their of the initial inoculation and it turns out that the group that got that half dose followed by a boost had a much higher rate of protection from covid19 disease than the group that got the dosing schedule that the company wanted to give to everybody

SOURCE: AstraZeneca Vaccine Trial Likely Needs a Restart: Johns Hopkins

Secondly, the “success” of these vaccines is not being measured by their ability to prevent infection with SARS-CoV-2, as many in the general public believe, but merely to lessen the severity of the symptoms associated with COVID-19, like coughs and headaches.

ANJALEE KHEMLANI: Do you anticipate that the first sets of vaccines out the door will be more of a less effective blocker of the virus?

FAUCI: Well that’s the primary—that’s a great question, and that’s the primary endpoint of most of the virus, is to prevent clinical disease. To prevent symptomatic disease, not necessarily to prevent infection.

SOURCE: Fauci Happy if Vaccine Permits Infection w/ Fewer Symptoms

Thirdly, the studies are touted as involving tens of thousands of people, but in Pfizer’s trial, only 170 of them were reported as being “diagnosed with COVID-19” during the trial. Of those, 162 were in the placebo group and eight were in the vaccine group. From this, it is inferred that the vaccine prevented 154/162 people from developing the disease, or “95%”. But as even the British Medical Journal points out, “a relative risk reduction is being reported, not absolute risk reduction, which appears to be less than 1%.”

Fourthly, the trials are still ongoing. Although several countries have now issued “emergency use authorization” allowing these companies to begin distributing these vaccines to the public, the stage III trials of the vaccines are ongoing, with several of the planned “endpoints” for the data not being collected for 24 months after injection. As a result, as even the UK’s own “Information for UK Healthcare Professionals” pamphlet regarding Pfizer’s vaccine points out, “Animal reproductive toxicity studies have not been completed,” meaning that, “It is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility.”

Even more chillingly, it is not healthcare professionals who are leading the charge to deliver this vaccine to the world, but the military

MURRAY BREWSTER: He commanded Canada’s NATO mission in Iraq. Now he’s in charge of making sure Canadians get the COVID vaccine.

TRUDEAU: Major General Dany Fortin will be heading up the logistics and operations within the centre.

SOURCE: Senior military commander to lead Canada’s COVID-19 vaccine distribution

SAMANTHA GALVEZ: Operation Warp Speed is a Department of Defense / CDC operation to distribute 300 million vaccines to the US.

MATTHEW YIENGST: As soon as the FDA authorizes an emergency use, if they chose to do so, we will move vaccine to all jurisdictions within 24 hours.

SOURCE: Adams County native plays vital role in military operation to distribute vaccine

RICHARD PASCOE: You know, we’re about to turn the corner here into 2021 and I think the American public should be very proud of what the army and the Department of Defense and our partners on the science side have done to bring these vaccines to the market.

SOURCE: Operation Warp Speed and US Army Role in Vaccine Distribution

BREWSTER: How much more involved the military will get is unclear. Public Health is still developing its plan. Defense Minister Harjit Sajjan acknowledges it is not beyond the realm of possibility in some parts of Canada troops could be running clinics and administering vaccine.

SOURCE: Senior military commander to lead Canada’s COVID-19 vaccine distribution

And most importantly, as incredible as this headlong rush to push an experimental vaccine on the majority of the world’s population is, it is even more incredible when it is revealed that Moderna and Pfizer’s vaccines are not, in fact, “vaccines” as anyone in the general public understands them. They are mRNA vaccines, a novel method of vaccination that has never before been approved for human use.

RHIJU DAS: So the concept of an RNA vaccine is: Let’s inject the RNA molecule that encodes for the spike protein.

ANGELA RASMUSSEN: It’s making your cell do the work of creating this viral protein that is going to be recognized by your immune system and trigger the development of these antibodies.

DAS: Our bodies won’t make a full-fledged infectious virus. They’ll just make a little piece and then learn to recognize it and then get ready to destroy the virus if it then later comes and invades us.

[. . .]

DAS: It’s a relatively new, unproven technology. And there’s still no example of an RNA vaccine that’s been deployed worldwide in the way that we need for the coronavirus.

RASMUSSEN: There is the possibility for unforeseen, adverse effects.

AKIKO IWASAKI: So this is all new territory. Whether it would elicit protective immune response against this virus is just unknown right now.

SOURCE: Can Scientists Use RNA to Create a Coronavirus Vaccine?

To be sure, the new mRNA vaccines work on an entirely different principle than any other vaccine that has ever been used on the human population. In order to understand that, it is important to understand the history of vaccine technologies.

The concept of “inoculation” has been around for centuries, with one of its earliest instances in China several centuries ago, where dried-out scabs of lightly infected smallpox sufferers were powdered and then blown up the nostrils of healthy people. The procedure aimed to infect the patient with a mild strain of smallpox, thus conferring immunity on them. This practice was brought over to Europe via Turkey and was eventually adopted around the world.

“Vaccination” developed in the late 18th century when Edward Jenner discovered that those who had been exposed to cowpox—a less virulent relative of smallpox—were themselves immune from smallpox. He “vaccinated” a boy with a cowpox vesicle from a milkmaid and then inoculated him with smallpox two months later. The boy did not develop smallpox, and the procedure was hailed as a breakthrough of medical science. The term “vaccination,” derived from the Latin word for cow, eventually came to refer to the general process of introducing immunogens or attenuated infectious agents into the body in order to stimulate the immune system to fight infections.

But this is not how mRNA vaccines function. In contrast to vaccination, which involves introducing an immunogen into the body, mRNA vaccines seek to introduce messenger RNA into the body in order to “trick” that body’s cells into producing immunogens, which then stimulate an immune response.

ELENA GUOBYTE: Two types of genetic vaccines are being investigated for COVID-19: mRNA and DNA. mRNA needs to reach the cytoplasm of host cells, while DNA needs to enter the nucleus. Then this genetic material gets taken up by the cell’s machinery, and the cell expresses the spike protein. These spike proteins are then recognized by the immune system, hopefully stimulating a protective response.

SOURCE: Coronavirus Vaccines – An Introduction

PAUL OFFIT: So the way this is going to work, the mRNA vaccine is—it’s the mRNA that codes for that coronavirus spike protein. You’re inoculated with that small little piece of genetic material. That genetic material then enters your cells and is is translated into a protein—in
this case, the coronavirus spike protein—which is then excreted from the cell. So, in essence, your body makes the spike protein and then your body makes antibodies to the spike protein, all because it’s been instructed to do that. Your cells have been instructed to do that by this little piece of messenger RNA.

SOURCE: How Do mRNA Vaccines Work?

NARRATOR: Protein factories in the cytoplasm, called ribosomes, bind to the messenger RNA. The ribosome reads the code in the messenger RNA to produce a chain made up of amino acids. There are 20 different types of amino acid. Transfer RNA molecules carry the amino acids to the ribosome. The messenger RNA is read three bases at a time. As each triplet is read, a transfer RNA delivers the corresponding amino acid. This is added to a growing chain of amino acids. Once the last amino acid has been added, the chain folds into a complex 3D shape to form the protein.

SOURCE: From DNA to protein – 3D

Any and all questions about this rushed, experimental vaccine technology are being labeled by the pharmaceutical manufacturers and the corporate press that runs on their advertising dollars as “anti-vax misinformation” and being actively censored. But despite the straw man argument that opposition to the vaccine comes solely from ignorant members of the public who are worried about being “injected with mircochips,” there are genuine concerns about the long-term safety of these vaccines coming from within the scientific community, and even from whistleblowers from within the ranks of the Big Pharma manufacturers themselves.

On December 1st, the former chair of the Parliamentary Assembly of the Council of Europe Health Committee, Dr. Wolfgang Wodarg, joined Dr. Michael Yeadon, a former Vice-President and Chief Scientific Officer at Pfizer Global R&D, to file a petition calling on the European Medicine Agency to halt the Phase III clinical trials of the Pfizer mRNA vaccine until they are restructured to address critical safety concerns associated with this experimental technology.

DEL BIGTREE: There is a petition now to try and stop the vaccine from being released in Europe and stop the trials in their tracks until some serious errors are fixed. The complaints are the potential dangers, if they are not rectified, of this vaccine. Let me very quickly just read through these before I bring on my next guest.

Here are the four major elements that are being pointed out by Dr. Wodarg and Dr. Yeadon.

The formation of so-called “non-neutralizing antibodies” can lead to an exaggerated immune reaction, especially when the test person is confronted with the real, “wild” virus after vaccination. This so-called antibody-dependent amplification, ADE, has long been known from experiments with corona vaccines in cats, for example. In the course of these studies all cats that initially tolerated the vaccination well died after catching the wild virus.

The mRNA vaccines from BioNTech/Pfizer contain polyethylene glycol (PEG). 70% of people develop antibodies against this substance – this means that many people can develop allergic, potentially fatal reactions to the vaccination.

The vaccinations are expected to produce antibodies against spike proteins of SARS-CoV-2. However, spike proteins also contain syncytin-homologous proteins, which are essential for the formation of the placenta in mammals such as humans. It must be absolutely ruled out that a vaccine against SARS-CoV-2 could trigger an immune reaction against syncytin-1, as otherwise infertility of indefinite duration could result in vaccinated women.

The much too short duration of the study does not allow a realistic estimation of the late effects. As in the narcolepsy cases after the swine flu vaccination, millions of healthy people would be exposed to an unacceptable risk if an emergency approval were to be granted and the possibility of observing the late effects of the vaccination were to follow. Nevertheless, BioNTech/Pfizer apparently submitted an application for emergency approval on December 1, 2020.

We’ve just updated you that that vaccine has been approved for the UK as we speak.

[. . .]

BIGTREE: What is it that people can do what—your fellow scientists and doctors—what do we need to do to make sure we don’t make one of the greatest scientific errors in human history?

WOLFGNG WODARG: Protect yourself and protect all your neighbors and friends so that they don’t get this vaccine. and you have to be—you have to show up, you have to tell the politicians that you will blame them for what they do with this. I think what what’s happening, it’s a great betrayal. We are betrayed. And people who betray normally are punished, and we won’t forget this if they go on doing this with us.

SOURCE: Health Expert: “Stop COVID Vax Experiments”

Before the combined weight of the pharmaceutical manufacturers, global health bodies, governments and the corporate media combined to suppress any questions about this unprecedented rush for a globally-distributed, experimental vaccine, there were widespread calls for caution from within the heart of the scientific community.

Even mainstream publications like Scientific American were compelled to note back in June of this year that there are reasons for concern over the way the COVID-19 vaccines are being rushed to market:

Telescoping testing timelines and approvals may expose all of us to unnecessary dangers related to the vaccine. While preclinical trials to evaluate the potential safety and efficacy of vaccine candidates are likely to include tens of thousands of patients, it is still unclear whether that number will be large enough and a trial will last long enough to evaluate safety for a drug that would be administered to so many. The US alone plans to vaccinate hundreds of millions of people with the first successful candidate. One serious adverse event per thousand of a vaccine given to 100 million people means harm to 100,000 otherwise healthy people.

The potential dangers of these vaccines—not just the mRNA vaccines that hijack your body’s cells to begin producing proteins to stimulate an immune response, but vaccines like AstraZeneca’s that uses a chimpanzee adenovirus to express the SARS-CoV-2 spike protein—are numerous. Not only do these vaccines present the potential for the antibody-dependent enhancement phenomenon that makes people more susceptible to the wild virus after having been vaccinated against it—which is a problem common to previous coronavirus vaccine candidates—but their potential impact on fertility has, even by the UK government’s own admission, not been tested at this point and remains “unknown.”

But even more fundamental than these particular safety concerns about these particular vaccines is the way that this fanatical, reckless and unprecedented headlong rush to push (and potentially even mandate) these vaccines on billions of people worldwide—women and children, young and old, healthy and unhealthy alike—is setting the most dangerous public health precedent in the history of humanity, a precedent that threatens to undermine our most cherished health freedoms in the name of a panic-induced “emergency.”

One of these core freedoms is the ability to refuse an experimental medical procedure, a freedom that was acknowledged in the Nuremberg Code of 1947 and enshrined in the International Covenant on Civil and Political Rights, which states that “no one shall be subjected without his free consent to medical or scientific experimentation.”

Despite the fact that the clinical trials surrounding these experimental vaccines are ongoing and that the FDA itself admits that there is “currently insufficient data to make conclusions about the safety of the vaccine in subpopulations such as children less than 16 years of age, pregnant and lactating individuals, and immunocompromised individuals” and “risk of vaccine-enhanced disease over time, potentially associated with waning immunity, remains unknown,” governments around the world are contemplating making these vaccinations mandatory, or compelling people to take them against their will by restricting their access to public life until they subject themselves to this medical experimentation.

ANCHOR: It’s a controversial idea that could end up being the law: “no jab, no job,” with some businesses considering making the COVID-19 vaccine mandatory for employees.

SOURCE: Coronavirus: Businesses considering making vaccine mandatory | 9 News Australia

CHRISTINE ELLIOTT: There may be some restrictions that may be placed on people that don’t have vaccines for travel purposes, to be able to go totheaters and other places. But that will be up to the individual person to decide.

SOURCE: COVID-19 vaccine won’t be mandatory, but those who don’t get it could face restrictions: Elliott

JO LING KENT: So here’s how it works: The app gives you a health pass to show before you go into big stadiums like this to streamline the process to make it safer and faster to get to your seat.

SOURCE: NBC Nightly News Broadcast (Full) – December 7th, 2020 | NBC Nightly News

TRACY GRIMSHAW: Alan, when there is a vaccine are you going to require all of your passengers to be vaccinated before they get on a plane?

ALAN JOYCE: Yeah we are looking at changing our terms and conditions to say for international travellers that we will ask people to have a vaccination before they can get on the aircraft.

SOURCE: Qantas boss says COVID-19 vaccination compulsory for international flights

The threat of forcing or compelling people to become unwilling guinea pigs in an ongoing medical experiment is immoral on its face. But even the prospect of enforcing such mandates would entail the erection of a surveillance and tracking system that further threatens basic rights and liberties. After all, in order to determine who has been vaccinated—and thus who is allowed to board an airplane or access a stadium or enter a store with a vaccine policy—there will need to be a system for identifying and tracking each vaccine recipient.

Whereas in days past, such tracking systems might have worked with identification papers, special badges to identify people’s status or other outwardly identifying marks, in the modern age, such schemes will take the form of digital apps and other technologically advanced methods for tracking, categorizing and identifying billions of people and their movements in real time.

There are already apps like IBM’s Digital Health Pass and CLEAR’s Health Pass that envision a world where our biometric ID will be linked via our smartphones to our health data in order to grant or deny access from public spaces and public events

NARRATOR: Here’s how Jane opens the CLEAR app and verifies her identity with a photo and real-time health insights. CLEAR’s developed touchless technology can take her temperature and confirm Jane is Jane so she can walk in with confidence

SOURCE: CLEAR Health Pass

NARRATOR: Your COVID-19 status will efficiently display as green, amber or red, dependent on your test results. This allows us to go about our daily activities in a safer way. We can all use health passport ireland in many ways, such as travel, hospitality, education, health care, construction, offices, entertainment, visits and much, much more.

SOURCE: Health Passport Ireland

Once the COVID vaccines are widely distributed, it would simply be a question of linking one’s vaccination record to the health pass app to prevent the unvaccinated from accessing any given space.

And while this future—sold through glossy corporate advertising but rejected by the vast majority of the public—may seem like a science-fiction dystopia, such systems are already being used to control the movements of people in China, where access to certain building or the ability to leave one’s own neighbourhood can be restricted to those whose phone-based apps show a “green” immunity status.

Worse, the COVID vaccine presents governments, intelligence agencies and corporations that have a direct interest in suppressing dissent, monitoring dissidents and controlling their populations with the perfect opportunity to make such systems a permanent fixture of daily life. After the immediate “threat” of the declared public health crisis subsides, the public is already being warned that these apps will be transitioned seamlessly into general monitoring of the population.

ANCHOR 1: Well during the summer spike, Palm Beach County launched something called a Combat COVID app. they spent a huge chunk of CARES Act money to do it. The app can alert you if you come into contact with a COVID positive person.

ANCHOR 2: The problem is it only works if there’s widespread use and there isn’t. So was this just a big waste of money?

[. . .]

DANIELLE WAUGH: Palm Beach County officials would not make anybody available for an interview for this story but I did get a written statement from a county spokesperson, who tells me they will still have use for this app even after the pandemic is over. He says they plan on transitioning its functions to be a more general community app.

SOURCE: Palm Beach County COVID app: Big investment, few users

As chilling as these “immunity passports” opening the door for governments to implement persistent digital tracking of their entire population is, it represents only the most visible privacy invasion that is being enacted on the back of this unprecedented vaccine rollout.

As viewers of the “Who Is Bill Gates?” documentary will know, these smartphone apps and voluntary reporting mechanisms will eventually be replaced by an even more invasive technological means of certifying vaccination. Not the “microchip” strawman that the fact checkers use to attempt to debunk these concerns, but the verifiable existence of a program to develop quantum dot tags to instantly identify who has received a given vaccine.

Late last year, Gates once again turned to Robert Langer and his MIT colleagues to investigate new ways to permanently store and record the vaccination information of each individual. The result of their research was a new vaccine delivery method. They found that by using “dissolvable microneedles that deliver patterns of near-infrared light-emitting microparticles to the skin,” they could create “particle patterns” in the skin of vaccine recipients which are “invisible to the eye but can be imaged using modified smartphones.”

Rice University describes the quantum dot tags left behind by the microneedles as “something like a bar-code tattoo.”

So who was behind this development? As lead researcher Kevin McHugh explains:

“The Bill and Melinda Gates Foundation came to us and said, ‘Hey, we have a real problem—knowing who’s vaccinated [. . .] So our idea was to put the record on the person. This way, later on, people can scan over the area to see what vaccines have been administered and give only the ones still needed.”

SOURCE: Who Is Bill Gates?

Experimental vaccine technologies. Rushed testing. Mandates and health apps. And, eventually, quantum dot tags and biometric IDs. The future that is coming into view on the back of this COVID nightmare is truly dystopian.

But as worrying as all of this, the most worrying aspect is the precedent that it sets for a new era of biosecurity. An era in which public health authorities will claim to have the right to force rushed, untested and experimental technologies on the public in the name of public “health.”

At the moment, these new technologies—like mRNA vaccines which reprogram cells to produce antigens or the DNA vaccines that seek to insert foreign genetic material directly into the cells’ nucleus and that even biotech giant Moderna admit “have a risk of permanently changing a person’s DNA”—are still understood by the public as “vaccines.” But they bare as little resemblance to the vaccines that have previously been given to the public as Edward Jenner’s cowpox vaccine bore to the old Chinese art of blowing smallpox scabs up the nose. And the medical technologies that are emerging now will once again utterly transform our understanding of “vaccines.”

One such technology is being actively developed by Profusa, Inc., a company that in 2016 received a $7.5 million grant from DARPA—the research and development agency of the US military—to “develop implantable biosensors that can continuously monitor multiple body chemistries.” Earlier this year, Profusa announced a study that will examine how the company’s technology—including a “wireless reader that adheres to the skin and collects and reports tissue oxygen levels” and a 3mm string of hydrogel, which can be inserted under the skin with a syringe and programmed to send “a fluorescent signal outside of the body when the body begins to fight an infection”—can be used to “develop an early identification system to detect not only disease outbreaks, but biological attacks and pandemics up to three weeks earlier than current methods.” The study is expected to be completed next year.

Hydrogels—networks of crosslinked polymer chains—are increasingly being turned to by proponents of these new technologies as potential delivery devices for drugs, cells, proteins, and bioactive molecules. In 2013, for instance, a team of European researchers announced a novel method for injecting a vaccine-containing hydrogel sphere to a spot beneath the skin, which could be released at a later time by swallowing a “stimulusresponsive biohybrid material.” Touted as a “remote-controlled vaccine delivery system,” the researchers proved their concept by injecting mice with a hydrogel containing human papillomavirus vaccine and later giving them a pill containing fluorescein, which dissolved the hydrogel mesh and released the vaccine. The research on this vaccine delivery method continues, with a Chinese team publishing research just this year on a self-adjuvanted hydrogel which “had both adjuvant potential and the ability to sustained release antigen.”

As viewers of the “Who Is Bill Gates?” documentary will know, the idea of implanting remote-controlled vaccines in large populations has been around since at least 2012, when, according to MIT Technology Review, Bill Gates personally asked MIT researcher Robert Langer to create an implantable birth control device that could be turned on or off remotely. The resulting device—a wireless birth control microchip that, as the National Post noted in 2014, “can be turned on and off with a remote control and that is designed to last up to 16 years”—was developed by Microchips Biotech, now part of Daré Bioscience, and has so far received $17.9 million in grant funding from the Bill & Melinda Gates Foundation.

From biolectronics to nanorobotics to synthetic biology, ever more incredible technologies are being pioneered that, whether or not they are marketed to the public under the catch-all term of “vaccine,” will operate in ways that are fundamentally unlike anything before used on the human population.

University of Ottawa researchers are working on creating “edible vaccines.”

Researchers at Harvard Medical School are developing autonomous DNA nanorobots capable of transporting molecular payloads directly into cells.

A team of scientists at Johns Hopkins University are working on shape-changing microdevices called “theragrippers” that can reside in the GI tract to aid in extended drug delivery.

Nanobots. Shape-changing bioelectronic devices. Remote-controlled vaccines. This is not the stuff of science fiction but of science fact, and the precedent that is being set during the COVID era to rush experimental and unproven medical technologies into use on the back of a declared crisis is the same precedent that could be used to foist these injectable technologies on the public in the future.

And, as Catherine Austin Fitts—former United States Assistant Secretary of Housing and Urban Development and founder of Solari, Inc.—explains, these injectables are part of an elaborate system of biological, economic, and political control that is being bankrolled into existence by powerful special interests.

CATHERINE AUSTIN FITTS: So let me go through where I think he’s going. I think where they’re going—and they’re they’re prototyping tons of technology, so I don’t think they have it yet—but where they want to go is they want to download a Microsoft Office system into your body, into your brain, and hook it up to the Jedi cloud contract and the Amazon Cloud contract at the CIA. And if they can get seven people seven billion people hooked up directly to their cloud contracts and use viruses—I mean, it’s very clever—use viruses to keep those updates coming. You know, just keep those updates coming.

So you saw my most recent article, “The Injection Fraud.” I think it’s a fraud to call these vaccines they’re not vaccines, they’re not medicine. But I think it’s the exact same model you used in the computers and the ideas. Just like Bill Gates made it possible for the intelligence agencies to get a backdoor into our—you know, our data—and our computers. They want a backdoor into our mind and it’s very hard if you haven’t if you haven’t looked into the creepy technology, the Charles Lieber kind of technology, it’s hard to fathom but we’re beginning to fathom it.

[. . .]

So what we have are people who have unimaginable liabilities for what they’ve done in the health area and what they’ve done in the financial area. And what they’re trying to do is they’re trying to do two things: one is to load an operating system into our bodies—I call it the injection fraud because they’re calling it a vaccine and under law a vaccine is medicine, this is not medicine, so to me what they’re up to is a fraud. And then the second thing they’re trying to do is implement contract tracing so they they can have—before they get the operating system in everybody they can have complete control. You know, kidnap you, put you in prison with no warrants, break into your house, take your kids.

And I keep saying to people: “Do you notice that it’s the people who flew Epstein Air who all want contract tracing? Why is that?” You know, why would you want the people who did Epstein Air to be able to come into your house and kidnap your kids?

SOURCE: Catherine Austin Fitts Exposes The Injection Fraud

Despite the protestations of those like Bill Gates who have a financial interest in these experimental vaccines, and the Big Pharma corporations that are selling these vaccines, and the governments that are being bribed by the international public health cartel to purchase these vaccines and pressure their public to accept them, and the corporate media who relies on these Big Pharma corporations for their advertising dollars, some facts about these novel coronavirus vaccines are indisputable:

They are the most rushed vaccines ever developed.
The manufacturers have been given total immunity from liability if their experimental vaccines cause injury.
The clinical trials testing the safety of these injections are not finished, meaning that every member of the public who takes one is now a human guinea pig in an ongoing medical experiment with the population of the planet.
The Pfizer and Moderna mRNA vaccines are themselves part of an experimental class of injection that has never before been given to the public;
These vaccines have not been tested for their ability to prevent infection or spread of SARS-CoV-2 and are not intended to do so.
And there is absolutely no long-term data about these vaccines to determine what their effects may be on fertility, the potential for pathogenic priming, or any other serious adverse reaction.

That this represents the most reckless and brazen experiment in the history of the world is undeniable on its face. Never before have billions of people been pressured to submit to a completely experimental, invasive medical procedure on the basis of a disease with a greater than 99% survival rate.

But large-scale, emergency vaccination campaigns have been tried before with sobering lessons about the danger of such a wide-scale experiment that are being deliberately ignored right now.

In the late 1950s and early 1960s, hundreds of millions of people were injected with polio vaccines that, years later, were discovered to have been contaminated with SV40, a cancer-causing virus found in the rhesus monkey kidney cells that were used to create the vaccine.

In 1976, twelve soldiers at Fort Dix were diagnosed with swine flu. This kicked off a round of public health hysteria that led the US government to mandate that every citizen in the country be vaccinated. In the end, only one soldier at Fort Dix died of the swine flu and no one outside of the base even tested positive for it, but the emergency immunization program went ahead. It was brought to an abrupt end after hundreds who had received the rushed vaccine began to display severe neurological disorders.

MIKE WALLACE: Remember the swine flu scare of 1976? That was the year the U.S. government told us all that swine flu could turn out to be a killer that could spread across the nation, and Washington decided that every man, woman and child in the nation should get a shot to prevent a nation-wide outbreak, a pandemic.

Well 46 million of us obediently took the shot, and now 4,000 Americans are claiming damages from Uncle Sam amounting to three and a half billion dollars because of what happened when they took that shot. By far the greatest number of the claims – two thirds of them are for neurological damage, or even death, allegedly triggered by the flu shot.

SOURCE: 60 Minutes Mike Wallace Exposes the 1976 Swine Flu Pandemic Vaccine Injuries

During the hysteria over swine flu in 2009, GlaxoSmithKline rushed a vaccine called Pandemrix to market in several European countries that was later associated with increased risk of narcolepsy. Years later, it was admitted that the 2009 flu season was no deadlier than any other flu season, but the British Medical Journal revealed that the body that advised the WHO on the declaration of the public health emergency that caused governments to purchase billions of dollars of vaccines was itself populated by advisors with direct financial ties to the Big Pharma vaccine manufacturers.

In each of these cases, the public was told to “follow the science,” and in each of these cases an unknown and perhaps unknowable number of people paid for that blind faith with their health. Now the revolver is once again being put to our heads and, with an assurance that that revolver probably contains a lot of empty chambers, the public is being asked to play Russian Roulette in the name of “trusting the science.”

NEIL DEGRASSE TYSON: I think we’re in the middle of a massive experiment worldwide. And that is—

STEPHEN COLBERT: —And we’re the guinea pigs?

TYSON: Maybe. The experiment is: will people listen to scientists?

SOURCE: Neil deGrasse Tyson On Coronavirus: Will People Listen To Science?

Surely those who wish to be the test subjects in this ongoing experiment should be free to make themselves into guinea pigs for the Big Pharma manufacturers. But every mandate or compulsion to force the vaccine on an unwilling recipient sets a dangerous precedent, a precedent that will one day lead to a tracked and surveilled population unable to resist the next generation of injectable bioelectronics.

This is not a game, this is not a test. Billions of people are being asked to participate in a gigantic experiment, not just an experiment in medical technology, but an experiment in compliance and blind trust.

The pressure to say yes and to go along with the crowd in this experiment is enormous. But if we lose the freedom to say “no” to this, then we may lose control over our bodily autonomy—and, ultimately, our humanity—forever.

The choice is ours . . . but for how much longer?

December 23, 2020 Posted by aletho | Civil Liberties, Science and Pseudo-Science, Timeless or most popular, Video | COVID-19 Vaccine | Leave a comment

What’s actually IN the US “Covid Stimulus Bill”?

The answer to that is nothing like as simple as you’d expect, given the name.

OffGuardian | December 22, 2020

The US congress just passed their Covid stimulus bill, or the “Consolidated Appropriations Act, 2021” to give its official title. So what’s actually inside it? What has just been passed into law?

The answers to that is “nobody really knows”, least of all the members of congress, who passed the law without reading it, as they so often do. It’s the longest bill in US history, at over 5500 pages and it sailed through the voting mostly sight unseen.

We’ve downloaded a copy of the full document and will embed it for those of you patient or masochistic enough to tackle the whole thing. We’ve read some already, and will point out the highlights:

“Foreign aid” is a big winner. Egypt is getting $1.3 billion, Sudan, Israel and Ukraine get over 500 million each, and many other countries around the world sizeable contributions, much of which will be spent on “defense”. Which is to say sent straight back to America via massive arms purchases.
Not all the money being sent overseas is for buying weapons, some is for backing coups. Venezuela and Belarus get special mention here, each getting their own section of the bill detailing how terrible their “illegal regimes” are. There’s also a large section on “combating Chinese influence”.
For some reason there’s another section on copyright law, which makes illegal streaming copyrighted content a federal crime, punishable by up to three years in prison.
Nearly 300 million is put aside to develop influenza vaccines and prevent a future influenza pandemic.
4 BILLION dollars for the Gates-funded GAVI, the Vaccine Alliance.
Vaccine “misinformation” is also a concern, and the bill provides for a pro-vaccine propaganda campaign – or rather a “PUBLIC AWARENESS CAMPAIGN ON THE IMPORTANCE OF VACCINATIONS”

So – huge amounts of foreign aid, support for various coups, totally irrelevant copyright laws, provisions for pro-vaccine propaganda campaigns… it’s not your typical “stimulus bill” so far, is it?

December 22, 2020 Posted by aletho | Civil Liberties, Corruption, Deception, Militarism | Covid-19, COVID-19 Vaccine, Human rights, United States | Leave a comment

Why you shouldn’t believe the COVID vaccine is effective

By Jon Rappoport | No More Fake News | December 21, 2020

I’ve covered the dangers of the vaccine. Now I want to show why it’s ineffective, even assuming the basic theory of vaccination is valid.

Peter Doshi, associate editor of the medical journal BMJ, and Eric Topol, Scripps Research professor of molecular medicine, wrote a devastating NY Times opinion piece about the COVID vaccine clinical trials.

They exposed the fatal flaw in the large Pfizer, AstraZeneca, and Moderna trials.

September 22, the Times : “These Coronavirus Trials Don’t Answer the One Question We Need to Know”:

“If you were to approve a coronavirus vaccine, would you approve one that you only knew protected people only from the most mild form of Covid-19, or one that would prevent its serious complications?”

“The answer is obvious. You would want to protect against the worst cases.”

“But that’s not how the companies testing three of the leading coronavirus vaccine candidates, Moderna, Pfizer and AstraZeneca, whose U.S. trial is on hold, are approaching the problem.”

“According to the protocols for their studies, which they released late last week, a vaccine could meet the companies’ benchmark for success if it lowered the risk of mild Covid-19, but was never shown to reduce moderate or severe forms of the disease, or the risk of hospitalization, admissions to the intensive care unit or death.”

“To say a vaccine works should mean that most people no longer run the risk of getting seriously sick. That’s not what these trials will determine.”

This means these clinical trials were dead in the water.

The trials were designed to show effectiveness in preventing mild cases of COVID—a cough, or chills and fever—which nobody should care about, because mild cases naturally run their course and cause no harm. THERE IS NO NEED FOR A VACCINE THAT PREVENTS MILD CASES.

Now I’ll explain WHY the clinical trials were only designed to show the vaccine could prevent mild cases.

The vaccine makers assume the SARS-CoV-2 virus is everywhere. Therefore, during the course of a clinical trial, the virus will descend from the clouds and infect a certain number of volunteers in the trial.

All those volunteers are healthy. They’re not old and frail. They’ve already been screened and eliminated, if they have a history of serious allergies.

So, when the SARS-CoV-2 virus attacks a few of these healthy volunteers, what are the odds it will cause serious cases of pneumonia, requiring hospitalization?

The odds are VERY long against.

How long do you think the vaccine makers would have to wait before, say, 150 of the healthy volunteers came down with serious pneumonia?

Five years? Ten? Forever?

Pfizer isn’t going to stand around and wait and wait and wait. Are you kidding?

No, they’re only going to wait until 150 volunteers (the preordained magic number) come down with a cough, or simple chills and fever—a mild COVID case.

Then they’re going to stop the clinical trial.

Then they’re going see how many of those 150 mild cases occurred in the people who got the vaccine, and how many cases occurred in the people who got the saltwater placebo shot.

This is how they find out how effective the vaccine is.

And indeed—according to Pfizer—most of the cases occurred in volunteers who got the saltwater placebo shot.

Therefore, Pfizer could claim the vaccine was effective in protecting against cough, or chills and fever. Mild cases of COVID.

That’s ALL Pfizer could say.

And THAT’S why the clinical trials were a failure. Because the trials were only set up to show prevention of mild cases—which nobody should care about.

I could go on and explain how the vaccine makers could fake even that useless claim, but I’ll leave it there.

The COVID vaccine is designed to prevent nothing important or significant.

All the rave reviews of the vaccine, the babbling about a historic breakthrough, the celebrations—complete and utter nonsense.

Jon Rappoport is the author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29^th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

December 22, 2020 Posted by aletho | Science and Pseudo-Science | COVID-19 Vaccine | Leave a comment

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ΑΛΗΘΩΣ

Some of the featured diagrams and instructions found in Reg 174

Section 4.6 of the official guidance recommends pregnant women should not recieve the BNT162b2 vaccine

Bell’s palsy causes drooping facial muscles similar to the effects of a stroke, image source PTHealth.com

Professor Sarah Gilbert at Oxford, Photo by John Cairns

Professor Adrian Hill at the Jenner Institute, Photo by John Cairns

Vaccitech’s homepage showing company co-founders Adrian Hill and Sarah Gilbert. From vaccitech.co.uk

The Wellcome Genome Campus, which houses the Wellcome Centre for Human Genetics, is located on the grounds of Hixton Hall, in Cambridgeshire, England.

A poster published by the Eugenics Society-Galton Institute in the 1930S, from the Wellcome Library

SixthSense | December 23, 2020

By Jon Rappoport | No More Fake News | December 24, 2020

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