A Nasty Shot in the Arm – RT-PCR Kits and Vaccines Unlicensed by Britain’s MHRA
Aware of the forthcoming vaccine roll-out aimed, it is said, to protect against a disease (COVID-19) that reached its apex almost nine months ago, I emailed the MHRA (Medical and Healthcare Regulatory Authority) on 20 November 2020.
My main concern is that people will unwittingly subject themselves to an experimental vaccine that has not been licensed by the MHRA, the ingredients of which have not been made public. Diagnosis of COVID-19 is made on the basis of a test, the RT-PCR test, the results of which are frequently flawed. I questioned if the MHRA had approved the RT-PCR test and copied in a medical doctor friend of mine.
“Since the reliability of the RT-PCR test has been questioned . . . it is important to know that the MHRA has done its duty in protecting the public from potentially harmful health-care products. Please reassure me that procedures have been followed and that this product the (RT-PCR test) has been approved by the authority. Thank you.”
The MHRA response was mind-blowing.
“There are literally 100s of CE marked Covid RT-PCR tests available on the EU market.
Such tests require a self-declaration process undertaken by the manufacturer with no review of performance data by any EU Government Body or Notified Body and that MHRA does not approve such products.
However, I can confirm that all PCR kits used by government laboratories or their subcontractors have been subject to rigorous validation by them before use.”
How can anyone possibly confirm that rigorous validation has taken place if these tests are not monitored?
It raised an alarm to think results from all the “100s” of RT-PCR tests which the UK government, and other governments of the world, use in checking for COVID -19 are reached using kits that are self-regulated “by the manufacturer”. It is more than disturbing. There is no authority reviewing the tests and no authority reviewing results from the tests. It was necessary to delve further.
“Who is checking how positive tests are arrived at? How many amplifications are being used in tests? Is this consistent across all testing stations?”
The answer, which did not address the questions, raised even more concerns, including the competency of the MHRA.
“There is no relation to vaccinating human volunteers and the use of an RT-PCR test.
I can also confirm that trials of the vaccines was approved by the normal rigorous processes.”
Whether intentionally, or through ignorance, both these sentences are blatantly false.
Within the last week the Assets Publishing Service of the UK government issued a document to Healthcare professionals on how to administer the PfizerBioNTech vaccine.
It quite clearly states that there is now, and since trials began always has been, a relationship between “vaccinating human volunteers and the use of an RT-PCR test.” In section 5.1 which discusses results from trials it explains the two criteria which were, and still are, being adopted:
“Confirmed cases were determined by Reverse Transcription-Polymerase Chain Reaction (RT-PCR) and at least 1 symptom consistent with COVID-19 disease*.
*Case definition (at least 1 of): fever, new or increased cough, new or increased shortness of breath; chills, new or increased muscle pain, new loss of taste or smell, sore throat, diarrhoea or vomiting.”
As to confirmation that vaccine trials were “approved by the normal rigorous processes” the whole document disproves any such claim. Approval has been granted on the basis of a measure only normally used in extreme emergencies, for example during the spread of “pathogenic agents, toxins, chemical agents or nuclear radiation.” It is called REG 174 (Regulation 174) a regulation which has recently been updated. Right at the start of the Assets Publishing Service document it states that:
“This medicinal product [REG 174] does not have a UK marketing authorisation but has been given authorisation for temporary supply by the UK Department of Health and Social Care and the Medicines & Healthcare products Regulatory Agency for active immunization to prevent COVID-19 disease caused by SARS-CoV-2 virus in individuals aged16 years of age and over.”
Whatever it is, it is not “normal rigorous” procedure. This vaccine is being rushed through in a process that can normally take up to ten years to complete. Even today no approved vaccine exists for SARS-COV from the 2003 epidemic, and indeed, no approval exists for any of the SARS/MERS family of viruses.
What is happening is a human experiment with a vaccine that has had minimal testing, of which the full recipe of ingredients is being kept secret.
That, in itself, ought to raise alarm – but the only alarms being raised seem to be of the nature whether people are wearing masks, obeying lockdown restrictions, washing their hands and social distancing.
We should be really worried about the Pfizer-BioNTech vaccine, and other vaccines, which contain ingredients designed to sterilize volunteers or change our DNA in a government-promoted scheme, the adverse results of which may not be known for decades.
Thanks to a GlaxoKlineSmith whistleblower whose evidence was presented on the David Knight Show (taken down by YouTube) we know that GKS was (is?) planning to use an ingredient in its COVID-19 vaccine, an anti-human chorionic gonadotropin (HCG) antigen, which causes infertility in women and in men. In men their testicles shrink, testosterone levels fall, the sperm is chemically attacked and dead sperm goes on to make women infertile too. In women. it:
“. . . produces antibodies which combine with HCG to render it biologically inactive . . . Out of 63 women they ][GSK] tested with HCG 61 of them became infertile. . . “
The last email I received from the MHRA confirmed my suspicion that this is a sensitive subject which the MHRA chooses to nip in the bud.
“I am sorry John but I do not have the time to deal with repeated communications with you as I am dealing with 100s of emails a day. This will be my last email to you.
The trials regarding vaccines have not been rushed through in terms of the MHRA’s involvement and we have applied the same level of scrutiny as it has historically done so for others.
The evidence that the vaccine is working or not depends on how many people contract the virus who have had the vaccine to those who have not been given it.”
His last sentence took me back full circle to my initial question about the reliability of the RT-PCR test which the MHRA has consistently neglected to monitor for accuracy, and which, despite assurance to the contrary, is being used in vaccine tests. The whole process reminded me of the plight of Daniel Doyce from Charles Dickens’ Little Dorrit.
Doyce was an engineer who tried to get his invention patented. For years he went backwards and forwards to the Circumlocution Office being sent from department to department without ever being given any constructive advice. Unable to make progress Doyce eventually took his creation abroad where he and it were a success. The trouble is with today’s regulatory authorities there is nowhere abroad to take our worries since the European Medicine Agency (EMA) is as complicit with Big Pharma’s aims as our own MHRA.
As the employee at MHRA did not have time “to deal with repeated communications” I emailed back to see if there was somebody else who could address my concerns. Previous correspondence had been answered quickly but it is two weeks now since I had a response to my last and I am not expecting another. When members of the public are worried about the safety and accuracy of medical products it is the MHRA’s duty to act.
Attempts to elicit the truth can be frustrating. It is in the interests of our families and friends, and their families and friends, to find out why the MHRA is not doing its job with regard to the RT-PCR test. Without doubt my questions have rattled the authority’s cage. Although it refuses to engage with me further I like to think there are others, concerned enough for their families and friends’ welfare and future on this beautiful planet of ours, who might wish to know why the RT-PCR test has not been given full scrutiny.
Close ties between big pharmaceutical conglomerates and their regulatory authorities raise suspicions as to their impartiality. In its questions and answers section the MHRA attempts to put these suspicions quietly to bed.
8. Why does the MHRA accept money from pharmaceutical industry? Isn’t this a conflict of interest?
Companies have to pay a fee for their marketing authorisation but we don’t seek business from them. Any complex licensing decisions are referred to the Agency’s independent advisory committees. These members must register any interests they have in the industry. They must declare any specific ones and take no part in discussions on that subject.
The agency’s independent advisory committees are another matter altogether and serious concerns have been raised as to how independent they really are. For example, in a June meeting of the Joint Committee on Vaccination and Immunisation, the minutes of which are still in draft form, we note that the Medical Advisor is Professor Jonathan Van Tam – a recent spokesman on the BBC promoting the virtues and safety of Pfizer BioNTech’s new vaccine while at the same time attempting to ameliorate public concern that these untested vaccines might indeed be dangerous.
Unlike most of the others on the committee Van Tam provides no conflict of interest details that are specific to COVID-19 vaccines. That does not mean he has none and contravenes a basic tenet of the MHRA’s dos and don’ts. University of Oxford Senior Associate Tutor, Tom Jefferson, exposed in 2017 the revolving door nepotism which saw the promotion of figures like Professor Van Dam and Sir Patrick Vallance to their present positions. Van Tam is one of three Deputy Chief Medical Officers to Professor Christopher Whitty, and it is not unusual for him to play down or choose not to mention his connections with pharmaceutical groups. As Jefferson notes: “Professor Van Tam’s track record as an ex-employee of Roche, Aventis Pasteur MSD and SmithKline Beecham (now GSK) has been excluded from the official DH press release . . .”
The “independent” CEO of the MHRA, Dr. June Raine, issued a statement on 19 November 2019, espousing the virtues of the Pfizer BioNTech vaccine trials.
She outlines the two routes available in approving a vaccine for use, namely, the emergency route (REG 174) which is now being made operational and the proper route which normally takes years. In these “new normal” days the MHRA has committed itself to “rigorously assess the data in the shortest time possible, without compromising the thoroughness of our review” regardless of which route is adopted. She fails to mention the RT-PCR test which is being used to determine results.
In the dangerous and untested vaccine experiments the unmonitored RT-PCR test is possibly the MHRA and the government’s weakest link. Interested parties can email the authority in the first instance at: MHRACustomerServices@mhra.gov.uk
A More Honest Perspective of the COVID-19 Pandemic
Since the first cases of the new coronavirus strain outside of China, every aspect of the pandemic’s ever-changing amoebic narrative has been carefully controlled by the World Health Organization and major government health agencies.
High officials within a syndicate of institutions, including the CDC, National Institute of Allergy and Infectious Disease and the UK’s National Heath Service, have largely dictated government responses to lessen the pandemic. The Sars2-Cov19 pandemic is not the first time unelected medical bureaucrats, who the average person assumes to possess an enduring expertise, have guided global policies against pandemics and serous infectious outbreaks. The most recent example was the 2009-2010 HIN1 Swine Flu pandemic that never truly happened according to plan. Subsequently that effort revealed a surprising incompetence in the international medical hierarchy that can be blamed on the entire system rather than a few inept individuals.
However, during the current pandemic scare, something unusual and remarkably radical has happened. Historically, voices of opposition within institutionalized medicine remain relatively silent. Most often it is only a handful of health professionals who come forward to challenge official statements or to uncover the serious flaws in the scientific literature to support their actions.
Yet for the past year we have witnessed tens of thousands of physicians, medical experts and researchers coming forward publicly with harsh and even damning criticisms of how the ruling medical agencies have mishandled the pandemic. They easily recognize these agencies’ contradictions, the conflicts of interest with the pharmaceutical industry, the large body of medical literature deconstructing and discrediting their fundamental claims, and the evidence to prove their policies are scientifically baseless. These are not dissident mavericks. Over 52,000 medical professionals representing some of the world’s leading medical schools and research institutions have already signed the Great Barrington Declaration in protest against the official Covid-19 strategies and these policies’ serious adverse effects on the physical and mental health of children, working class citizens and the poor. Moreover, they have nothing to gain. No financial interests jeopardize their judgments. And they are fully aware of the pushback and blacklisting that may follow and would injure their reputations.
Around the world, dissident medical voices are warning us that:
The official death counts, particularly in the US and the UK are grossly exaggerated
Polyermase chain reaction (PCR) was never created to be used as a diagnostic tool to determine Covid-19 infection or any other virus. Overreliance upon PCR is a travesty that has created a Case-pandemic rather an actual symptomatic scourge.
The evidence to support the belief that large social lockdowns and social distancing, perhaps even mask wearing, will deter the spread of the virus is overstated and inaccurate.
America’s official narrative, where the number of cases per capita far surpass any other nation, that effective, safe and cheaper drugs such as Ivermectin and hydroxychloroquine (HCQ) have no value and post serious harm is completely unfounded. Rather, if used wisely it is highly effective and safe as a preventative measure for first stage treatment of mild and moderate infections.
A compilation of 210 studies on HCQ’s effectiveness against Covid-19, 145 peer reviewed, only found 26 showed that the cheap, widely used drug posed some risks or was ineffective. The remainder clearly indicate that HCQ is one of our best and most reliable courses of treatment. For example a study of 585 patients treated with HCQ along with azithromycin and zinc were relieved in under 3 days and none were hospitalized, required ventilation or died. Another study published in the journal Clinical and Translational Science reported 73% reduction in hospitalization with no serious adverse events.
In the meantime, we are told we must await for a vaccine or a new miracle drug and no other medical intervention is warranted other then personal hygienic practices, masks and social distancing.
The New York Times and other major media outlets are misrepresenting new cases of Covid-19 with the actual disease thereby grossly inflating those who may be positive but are otherwise healthy and pose no public threat.
The WHO’s, CDC’s and NHS’ internal confusion and culture of inconsistency is leaving more and more citizens questioning who can be trusted. Even the otherwise conservative British Medical Journal published a rare and brutal condemnation of the corruption and commercialization throughout the official Covid-19 narrative. BMJ’s executive editor Kamran Abbasi wrote:
“Science is being suppressed for political and financial gain. Covid-19 has unleashed state corruption on a grand scale, and it is harmful to public health.1 Politicians and industry are responsible for this opportunistic embezzlement. So too are scientists and health experts. The pandemic has revealed how the medical-political complex can be manipulated in an emergency—a time when it is even more important to safeguard science.”
Sadly mainstream media such as the New York Times, Washington Post and BBC are revealing a lack of journalistic integrity despite the open accessibility of medical studies to the contrary. Instead the media serves as an echo chamber to continue advancing this international debacle created by our leading health officials.
To understand the miscalculation of deaths that can be directly attributed to Covid-19 we can begin with the CDC’s own website:
“Due to the ongoing COvID-19 pandemic, this system will suspend data collection for the 2020-2021 influenza season.”
In other words, the CDC’s monthly mortality reports will no longer be monitoring actual influenza deaths, which are more often than not also comflated with deaths due to pneumonia. William Briggs, a former professor at Cornell University noted that last summer the CDC ceased counting flu and pneumonia deaths “because, we suppose, of the difficulty telling these deaths from doom deaths [Covid-19].” So how will these deaths be entered into mortality reports?
In early December, an assistant director at Johns Hopkins Medical School’s Department of Applied Economics examined death statistics during the Covid pandemic and previous years. Due to the high percentage of non-Covid deaths decreasing during the pandemic, her conclusion was that these deaths were intentionally being labeled as Covid-1 caused. Her colleague Dr. Yanni Gu summarized the problem:
“The CDC classified all deaths that are related to Covid-19 simply as Covid-19 deaths. Even patients dying from other underlying diseases but are infected with Covid-19 count as Covid-19 deaths. This is likely the main explanation as to why Covid-19 deaths drastically increased while deaths by all other diseases experienced a significant decrease.”
This irrational discrepancy in causes of death is not solely an American problem. Globally there has been a 98% percent decrease in diagnosed flu cases compared to 2019. Australia alone has recorded a 96% drop off.
There may be a sensible way to explain the decrease in flu and this in turn helps explain the dramatic increase in Covid-19 cases due to inaccurate testing and an infestation of false positives. Given the enormous impact of lockdowns, closing of businesses and public spaces, social distancing and masks, it is feasible that flu rates would decline noticeably. However, then the rise in Covid-19 cases becomes completely nonsensical unless spurious testing is the culprit.
Recently, even the World Health Organization had to acknowledge PCR’s failures. Despite the mincing of words, the WHO reported,
“The design principle of RT-PCR means that for patients with high levels of circulating virus (viral load), relatively few cycles will be needed to detect virus so the Ct [cycle threshold] will be low. Conversely when specimens return a high Ct value, it means that many cycles were required to detect the virus. In some circumstances, the distinction between background noise and actual presence of the target virus is difficult to ascertain”
Most testing labs are using a cycle threshold of 40 amplifications, consequently the high rate of false positives. This is the reason for cases rising exponentially while actual deaths had leveled in mid summer until more recently. In the UK, Public Health England states, “if a person has both a negative and positive test, then only their positive test will be counted.” The US does likewise.
University of California virologist Dr. Juliet Morrison stated, ‘I’m shocked that people think that 40 [cycles] could represent a positive.” She recommends a reasonable cutoff at 35, and Dr. Michael Mina at Harvard’s School of Public Heath suggests 30 or less. University of North Carolina’s director of clinical microbiology Melissa Miller has called the application PCR for all situations “completely irresponsible.”
The most damning indictment against every governor across the US who continues to rule on lockdowns, school closures and draconian police enforcement and yet has failed to reign in the plague of erroneous PCR testing in his or her state is found in a recent study by the Infectious Diseases Society of America. Using as a low a 25 cycle threshold, 70% of positives were not actual cases because the virus was unable to be cultured. In other words, the virus was already dead.
And yet when PCR cycle thresholds are adjusted, the number of cases plummet. This was observed in efforts made in Massachusetts, New York and Nevada where it was discovered that 90% of those testing positive carried “barely any virus.”
Fortunately some countries are waking up to PCR’s unreliability that was originally perpetuated by a very entrepreneurial German doctor Christian Dosten. Dosten also happens to be an advisor to the Germany’s Federal Ministry of Health. A Portugal appeals court ruled PRC is unreliable for testing Covid-19 and any enforced quarantine based on a positive PCR test would be illegal. As for Dosten and his paper published in the journal Eurosurveillance, it has served as the rationale for widespread PCR use. But the paper is substantially inaccurate but helped serve as a means for Dosten to gain a patent for coronavirus PCR testing. Now 22 leading medical professionals from the International Consortium of Scientists in Life Sciences have filed for the paper’s retraction due to “a tremendous number of very serious design flaws… which make the PCR test completely unsuitable as a diagnostic tool to identify the SARS-CoV-2 virus.”
The real crime is that none of the above failures were inevitable.
There is no reasonable explanation for miscalculating actual deaths associated with Covid-19 other than shear stupidity or gross intentional neglect. PCR’s unsuitability to accurately diagnose the presence of active Covid-19, or any other infectious virus, has been well documented for many years. Even PCR’s inventor Dr. Kary Mullis has stated it is unsuited for clinical diagnosis.
Yet despite all of the foreknowledge of these facts, countless people have had their lives devastated by the choices our federal health officials and politicians have made based upon severely flawed science. Unnecessary quarantining, loss of income, lockdowns, and mental stress have adversely effected millions of Americans and people around the world. Again, we might to turn Abbasi’s article in the BMJ:
“… as the powerful become more successful, richer, and further intoxicated with power, the inconvenient truths of science are suppressed. When good science is suppressed, people die.”
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.
Full transcript below.
***
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.
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.
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.
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.
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.
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.
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.”
. . .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.
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.
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.
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.
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
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.
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 Journalpoints 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.
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.
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.
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.
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.
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.
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.
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.
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 enhancementphenomenon 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.
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.
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.
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.
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
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.
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.
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.”
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 researchjust 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?
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.
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?
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.
