COVID-19 VACCINES IMPORTANT POINTS
Please Share with Your Family and Friends
MINOR IMPACT: Vaccine manufacturers claim that Covid-19 vaccines are 95 percent “effective,” but the FDA is allowing companies to define effectiveness as “prevention of mild symptoms.” The studies are not designed to detect a reduction in outcomes such as severe illness, hospitalization or death.(1,2) For individuals who develop severe symptoms, the vaccine is not a remedy. Instead, nutritional and oxidative support can help keep the illness from going into “overdrive.”(3)
EXPECT ADVERSE REACTIONS: Participants in every Covid-19 vaccine trial have reported adverse reactions including high fever, chills, muscle pains and headaches. (4-6) Some have even reported severe reactions that required hospitalization and invasive treatment. According to the FDA, potential long-term effects may include Guillain-Barré syndrome, brain swelling, muscle weakness and paralysis, convulsions and seizures, stroke, narcolepsy, shock, heart attack, autoimmune disease, arthritis and joint pain, multisystem inflammatory syndrome in children, and death.(7) Some UK health workers have experienced anaphylactic shock after receiving one dose of the approved vaccine.8
WON’T PREVENT COVID-19: An FDA Pfizer briefing paper published December 10, 2020 revealed 43 percent more suspected cases of Covid-19 in the vaccinated group than in the placebo group within seven days of vaccination.(9)
NO LIABILITY: Covid-19 vaccine manufacturers will be protected from all liability—if you are injured, you cannot sue. (10) Manufacturers will have complete indemnity even though all previous attempts at creating coronavirus vaccines caused harm and never advanced to regulatory approval. (11)
WILL NOT END RESTRICTIVE MEASURES: Dr. Anthony Fauci of the National Institutes of Health acknowledges that the vaccines may prevent symptoms but will not block spread of the virus, so vaccine recipients will still need to wear masks, practice social distancing and avoid crowds. (12,13)
NOT NECESSARY: According to the CDC’s current best estimate, the “infection fatality rate” (IFR) for Covid-19 is less than 1 percent for people age 69 and younger, including a .003 percent IFR for children and adolescents. (14)
COULD MAKE YOU STERILE: Two prominent doctors, including the ex-head of Pfizer’s respiratory research, warn that Covid-19 vaccines contain a spike protein called syncytin-1, vital for the formation of the placenta.15 If the vaccine triggers an immune response to this protein, then female infertility, miscarriage or birth defects could result.
FOR FURTHER INFORMATION (including printable flyers): https://www.westonaprice.org/covid-19-vaccines-important-points/
1. Doshi P. Will covid-19 vaccines save lives? Current trials aren’t designed to tell us. BMJ. 2020;371:m4037. https://www.bmj.com/content/371/bmj.m4037.
2. Haseltine WA. Covid-19 vaccine protocols reveal that trials are designed to succeed. Forbes, September 23, 2020. https://www.forbes.com/sites/williamhaseltine/2020/09/23/covid-19-vaccine-protocols-reveal-that-trials-are-designed-to-succeed/?sh=5da0663d5247.
3. Brownstein D, Ng R, Rowen R et al. A novel approach to treating COVID-19 using nutritional and oxidative therapies. Science, Public Health Policy, and the Law. 2020;2:4-22. https://ozonewithoutborders.ngo/wp-content/uploads/2020/07/Novel-Approach-to-Covid-19.pdf.
4. Jackson LA, Anderson EJ, Rouphael NG et al. An mRNA vaccine against SARS-CoV-2 – preliminary report. New England Journal of Medicine. 2020;383(20):1920-1931. https://www.nejm.org/doi/full/10.1056/NEJMoa2022483.
5. Allen A, Szabo L. NIH “very concerned” about serious side effect in coronavirus vaccine trial. Scientific American, September 15, 2020. https://www.scientificamerican.com/article/nih-very-concerned-about-serious-side-effect-in-coronavirus-vaccine-trial/.
6. Mayer A. Leading COVID vaccine candidates plagued by safety concerns. The Defender, November 13, 2020. https://childrenshealthdefense.org/defender/covid-vaccine-candidates-safety-concerns/?itm_term=home. .
7. U.S. Food and Drug Administration. Vaccines and Related Biological Products Advisory Committee, October 22, 2020 Meeting Presentation, slide #16. https://www.greenmedinfo.com/blog/covid-19-vaccine-bombshell-fda-documents-reveal-death-21-serious-conditions-possi1.
8. Reals T. U.K. warns against giving Pfizer vaccine to people prone to severe allergic reactions. CBS News, December 9, 2020. https://www.cbsnews.com/amp/news/covid-vaccine-pfizer-shot-uk-warning-people-with-history-of-significant-allergic-reactions/#app.
9. https://www.fda.gov/media/144245/download, page 42.
10. Public Readiness and Emergency Preparedness Act. COVID-19 PREP Act Declarations. https://www.phe.gov/Preparedness/legal/prepact/Pages/default.aspx.
11. Lyons-Weiler J. Pathogenic priming likely contributes to serious and critical illness and mortality in COVID-19 via autoimmunity. Journal of Translational Autoimmunity. 2020;3:100051. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142689/.
12. Khemlani A. Fauci: Early COVID-19 vaccines will only prevent symptoms, not block the virus. Yahoo! Finance, October 26, 2020. https://finance.yahoo.com/news/fauci-vaccines-will-only-prevent-symptoms-not-block-the-virus-195051568.html.
13. Scipioni J. Dr. Fauci says masks, social distancing will still be needed after a Covid-19 vaccine—here’s why. CNBC, November 16, 2020. https://www.cnbc.com/2020/11/16/fauci-why-still-need-masks-social-distancing-after-covid-19-vaccine.html.
14. Centers for Disease Control and Prevention. COVID-19 pandemic planning scenarios. Updated September 10, 2020. https://www.cdc.gov/coronavirus/2019-ncov/hcp/planning-scenarios.html.
15. Petition/motion for administrative/regulatory action regarding confirmation of efficacy end points and use of data in connection with the following clinical trials. Dr. Wolfgang Wodarg and Dr. Michael Yeadon, petitioners. Filed with European Medicines Agency, December 1, 2020. https://healthimpactnews.com/wp-content/uploads/sites/2/2020/12/Wodarg_Yeadon_EMA_Petition_Pfizer_Trial_FINAL_01DEC2020_EN_unsigned_with_Exhibits.pdf.
: Vaccine manufacturers claim that Covid-19 vaccines are 95 percent “effective,” but the FDA is allowing companies to define effectiveness as “prevention of mild symptoms.” The studies are not designed to detect a reduction in outcomes such as severe illness, hospitalization or death.1,2 For individuals who develop severe symptoms, the vaccine is not a remedy. Instead, nutritional and oxidative support can help keep the illness from going into “overdrive.”3
(Please note that I have excerpted a good deal of the text which is available at the link below)
Sausage Making at FDA: How Human Cancer Cells Got Into Vaccines
In a 2012 meeting, the FDA voted to allow the use of human fetal cells and adult human tumor cells in vaccines, despite acknowledging the many risks, including that vaccine recipients might later develop cancer.
“If the American people knew some of the things that went on at the FDA, they’d never take anything but Bayer aspirin.” — Len Lutwalk, FDA scientist
“The FDA, by spinelessly knuckling under to every whim of the drug companies, has thrown away its high reputation, and in doing so, forfeited our trust.” — Drummond Rennie, deputy editor of JAMA
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Vaccines and related biological products advisory committee today
Today — Thursday, Dec. 10 — the Vaccines and Related Biological Products Advisory Committee (VRBPAC), which is the U.S. Food and Drug Administration’s (FDA) internal panel that licenses new vaccines as “safe and effective,” will meet to consider Pfizer’s COVID vaccine. VRBAC will meet in one week, Dec. 17, to consider approval of the Moderna vaccine.
The damning safety studies in Pfizer’s late release clinical trial data dump, and the severe (life-threatening) allergic reactions that bedeviled the vaccine’s UK rollout, have raised red flags and public anxiety about the safety of the companies’ mRNA vaccines. Anthony Fauci has addressed growing skepticism about COVID vaccines and the Operation Warp Speed program, by reassuring the public that “VRBPAC” is an “independent panel of leading experts” whom the public can absolutely trust to assure vaccine safety.
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How FDA originally approved use of fetal cells in vaccines
FDA allows both human fetal cells and adult human tumor cells in vaccines. Both types have cancer risks. While both Pfizer and Moderna tested their mRNA vaccine using fetal cells, there are no fetal cells, cell debris or DNA in their final products.
However, according to company documents, Johnson and Johnson (Janssen) and Altimmune’s COVID vaccines are manufactured in the human fetal cell line PER-C6, and thus the final vaccine products will contain cellular debris and DNA fragments from these cells. Researchers harvested these cell lines from the eyeball of an 18-week-old human fetus aborted in 1985, and then rendered them immortal by making them cancerous.
The AstraZeneca, Cansino, Gamayela, Vaxart, LongComm and Upitt vaccines are manufactured in the human fetal cell line HEK293, and thus the final vaccine products will contain cellular debris and DNA fragments from the fetal HEK-293 cell line. Scientists harvested this cell line from the kidney of a female Dutch fetus legally aborted in 1973 and then immortalized the cells by rendering them cancerous.
Normal primary cells, which are unable to replicate indefinitely, ultimately die. Immortalized cell lines are derived from known malignant cancer cells such as those obtained from Henrietta Lacks (HeLa) or created in the laboratory by introducing viral oncogenes or chemical exposures capable of mutating normal primary cells into immortal tumor cells.
According to FDA’s “The Pink Sheet” dated Nov. 29, 1999, for two decades the agency has been acutely aware of the inherent risks of using immortalized cell lines for vaccine development. The FDA CBER Director Dr. Peter Patriarca, M.D. explained that continuous cell lines are used for their ability to self-propagate, making them an ideal substrate on which to grow viruses, “the worst thing we are concerned about is … malignancy, because some of these continuous cells have the potential for growing tumors in laboratory animals.”
Patriarca further conceded that “the technology to make these vaccines actually exceeds the science and technology to understand how these vaccines work and to predict how they will work.” …
We call vaccines “biologics” because vaccinologists have traditionally grown their antigens on biological substrates — usually animal tissue. Competing companies culture COVID vaccines on a variety of animal strata. The Merck and IAVA COVID vaccines are manufactured in vero monkey cells, and thus contain cellular debris and DNA fragments from vero monkeys in the final product. The Sanofi, GSK, and Novavax COVID jabs are manufactured in insect cells and thus contain insect cellular debris and DNA fragments in the final products.
Public health advocates criticize the use of animal tissues in vaccines due to risks that they carry endogenous viruses, microbes, parasites and lack safety testing. (Plague of Corruption, Mikovits 2020). …
Researchers and regulatory agencies have worried for more than 50 years about the potential for injected DNA to cause cancer. …
Regulators have in the past predicted that the odds of that happening were less than 1 in a trillion. However, in early gene therapy trials this event did indeed occur in 4 of 9 boys, 1 of whom died from the leukemia the insertions caused.
But as corrupt as FDA is, the internal panels — VRBAC — that approve new vaccines make the rest of the agency look like a Sunday church picnic.
When Dr. Fauci, Paul Offit, Peter Hotez and Bill Gates tell you that you needn’t worry because FDA is the “gold standard” for vaccine safety and that the ultimate licensing decision will be made by an “independent panel of experts,” they are talking about VRBPAC. But VRBPAC is far from “independent.” It is not even comprised exclusively of public officials. Instead, it is populated by outside “experts” who are almost all pharmaceutical industry insiders.
In 2003, following a 3-year investigation, the United States Congress’s House Oversight Committee found VRBAC was completely dominated by the vaccine industry.
“Examples of Conflicts of Interest:
“For instance, 3 out of 5 FDA advisory committee (VRBPAC) members who voted to approve the rotavirus vaccine in December 1997 had financial ties to pharmaceutical companies that were developing different versions of the vaccine.
“One out of five voting members’ employer had a $9,586,000 contract for a rotavirus vaccine.
“One out of five voting members was the principal investigator for a Merck grant to develop a rotavirus vaccine.
“One out of five voting members received approximately $1 million from vaccine manufacturers toward vaccine development.”
Congressional investigators concluded that, “Altogether, four out of the five committee members had conflicts of interest that required waivers, and their recommendation for approval of the vaccine was unanimous.”
Here’s what happened at the 2012 FDA meeting on fetal cells
HHS acknowledges that the FDA and Centers for Disease Control committees that contract and review new vaccines have historically not used “evidence-based medicine.” To illustrate what this means, one only need read (below) the astonishing transcript of the 2012 panel that first approved the use of adult cancer tumor cells in vaccines.
This transcript shows what the public is never supposed to see: the behind-the-scenes sausage-making of federal vaccine approvals. Here, you will read for yourself how the “independent,” “gold standard” panelists entrusted with protecting your children made monumentally consequential decisions, not on evidence-based science, but by rolling the dice and taking what they knew was a horrendously risky bet on public health
In any other realm, this transcript would be proof of negligent homicide. … We are all lab rats in their high-risk population-wide experiment. At FDA’s vaccine division, that sort of reckless decision-making is routine.
In 2012, most live virus vaccines were from animal tissue and the idea of putting potentially cancerous tumor cells from adult “donors” in vaccines was still a daring and audacious gamble. That September, the FDA VRBPAC committee met to discuss this risky innovation. The transcript of that meeting — showing captive FDA officials considering a proposal by the pharma cabal to allow the use of human cancer cells (HeLa) to replace animal tissue in the manufacture of vaccines — is proof of reckless criminal conduct.
Unbelievably, FDA voted to allow pharmaceutical companies to produce vaccines using human cells without reviewing a single scientific study to determine if the outcome would be safe.
Before, I quoted some of the criminally reckless statements from the meeting directly. A more detailed account appears in this article.
This was a full meeting of FDA’s VRBPAC in 2012 to decide on the use of human tumor cell lines for the production of vaccines. I list these speakers and their titles at that time:
Dr. Philip Krause, Acting Deputy Director of OVRR (Office of Vaccine Research and Review) and FDA’s CBER (Center for Biologics Evaluation and Research). Also, Principal Investigator for Vaccine Safety: Virus Detection and Latency.
Dr. Doug Lowy, Director of the National Cancer Institute of the NIH.
Dr. Robert Daum, Chair of the VRBPAC.
Donald W. Jehn M.S., Designated Federal Officer for VRBPAC.
Keith Peden, PhD, Chief of LDNAV, DVP/OVRR/CBER.
Dr. Marion Gruber, Director of the FDA’s Office of Vaccines.
Dr. Nathanial Brady, a self-described clinician.
Dr. Pamela McInnes, a vaccine development expert and the Director of the Division of Extramural Research at the NIH’s National Institute of Dental and Craniofacial Research, and previously a Deputy Director under Anthony Fauci at the National Institute of Allergy and Infectious Diseases.
Pharma knew that their tumorigenic vaccines might cause tumors in recipients.
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FDA officials knew that tumors might occur decades after vaccination.
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FDA openly acknowledged that its primary objective was not to assure public safety but to help vaccine manufacturers.
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FDA officials knew that they could not prove vaccine safety using test animals to assess oncogenicity.
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FDA officials deliberately terminated animal safety tests too early in order to conceal consequences.
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FDA decided to keep the tumor cell lines secret, because doctors and the public may be alarmed and say “Oh, my God!” if they knew the truth.
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FDA decided to use deceptive language to convince doctors and the public that the vaccines were safe even when they, themselves, were unconvinced of safety.
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FDA decided to hide information about their use of tumor cells and omit it from package inserts.
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Health authorities were skeptical about safety of the tumor lines, but they decided to subject the public to the risk, so that they could perform a global population-wide live human experiment.
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FDA officials opted to toss the dice, perform the population-wide human experiment, and learn about the risks as time goes by.
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The committee formally approves the method of making vaccines from human cancer tumors.
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Prior to voting to go forward, the committee made the following conclusions:
Making vaccines with cells that are directly derived from human cancer tumors is faster and cheaper than breeding animals for the culture media.
Millions of potentially cancer-causing vaccines will be produced.
The vaccines may possibly cause genetic mutations.
Millions of dollars will be made by vaccine promoters.
The health of millions of consumers may be jeopardized.
Information about how vaccines are made will be hidden from doctors and
Finally, it’s worth considering that cancer treatment drugs like Keytruda are among pharmaceutical companies’ largest profit makers. Precipitating a cancer epidemic in human populations only benefits vaccine makers’ bottom line.
Remember, these are the same companies and the same FDA regulators that brought us the opioid epidemic.
Groundbreaking research indicates that most of what is believed about the purportedly deadly properties of viruses like influenza is, in fact, not evidence-based but myth.
Germ theory is an immensely powerful force on this planet, affecting everyday interactions from a handshake, all the way up the ladder to national vaccination agendas and global eradication campaigns.
But what if fundamental research on what exactly these ‘pathogens’ are, how they infect us, has not yet even been performed? What if much of what is assumed and believed about the danger of microbes, particularly viruses, has completely been undermined in light of radical new discoveries in microbiology?
The hyperbolic manner in which health policymakers and mainstream media pundits talk about it today, flu virus (or COVID-19) is an inexorably lethal force (note: viruses are obligiate parasites, at worst, with no inner motive force to actively “infect” others), against which all citizens, of all ages 6 months or older, need the annual influenza vaccine to protect themselves against, lest they (it is said) face deadly consequences. Worse, those who hold religious or philosophical objections, or who otherwise conscientiously object to vaccinating, are being characterized as doing harm to others by denying them herd immunity (a concept that has been completely debunked by a careful study of the evidence, or lack thereof). For instance, in the interview below Bill Gates tells Sanjay Gupta that he thinks non-vaccinators “kill children”:
But what if I told you that there isn’t even such a thing as “flu virus,” in the sense of a monolithic, disease vector existing outside of us, conceived as it is as the relationship of predator to prey?
First, consider that the highly authorative Cochrane collaboration acknowledges there are many different flu viruses that are not, in fact, influenza A — against which flu vaccines are targeted — but which nonetheless can contribute to symptoms identical to those attributed to influenza A:
“Over 200 viruses cause influenza and influenza-like illness which produce the same symptoms (fever, headache, aches and pains, cough and runny noses). Without laboratory tests, doctors cannot tell the two illnesses apart. Both last for days and rarely lead to death or serious illness. At best, vaccines might be effective against only Influenza A and B, which represent about 10% of all circulating viruses.” (Source: Cochrane Summaries).” [emphasis added]
This makes for a picture of complexity that powerfully undermines health policies that presuppose vaccination equates to bona fide immunity, and by implication, necessitates the herd collectively participate in the ritual of mass vaccination campaigns as a matter of life-or-death social necessity.
Even the use of the word “immunization” to describe vaccination is highly misleading. The moment the word is used, it already presupposes efficacy, and makes it appear as if non-vaccinators are anti-immunity, instead of what they actually are: pro-immunity (via clean air, food, water, and sunlight), but unwilling to subject themselves or their healthy children to “unavoidably unsafe” medical procedures with only theoretical benefits.
Why Flu Virus Doesn’t Exist (The Way We Were Told)
But the topic gets even more interesting when we consider the findings of a 2015 study entitled “Conserved and host-specific features of influenza virion architecture.” This was the first study ever to plumb the molecular depths of what influenza virus is actually composed of. Amazingly, given the long history of vaccine use and promotion, the full characterization of what proteins it contains, and where they are derived from, was never previously performed. How we invest billions of dollars annually into flu vaccines, and have created a global campaign to countermand a viral enemy, whose basic building blocks were not even known until a few years ago, is hard to understand. But it is true nonetheless.
The study abstract opens with this highly provocative line:
“Viruses use virions to spread between hosts, and virion composition is therefore the primary determinant of viral transmissibility and immunogenicity.” [emphasis added]
Influenza viral particles
Virion are also known as “viral particles,” and they are the means by which viral nucleic acids are able to move and ‘infect’ living organisms. Without the viral particle (taxi) to carry around the virus DNA (passenger), it would be harmless; in fact, viruses are often described as existing somewhere between living and inanimate objects for this reason: they do not produce their own energy, nor are transmissable without a living host. And so, in this first line, the authors are making it clear that virion composition is also the primary determinant in how or whether a virus is infectious (transmits) and what effects it will have in the immune system of the infected host.
This distinction is important because we often think of viruses as simply pathogenic strings of DNA or RNA. The irony, of course, is that the very things we attribute so much lethality to — viral nucleic acids — are not even alive, and can not infect an organism without all the other components (proteins, lipids, extra-viral nucleic acids) which are, technically, not viral in origin, participating in the process. And so, if the components that are non-viral are essential for the virus to cause harm, how can we continue to maintain that we are up against a monolithic disease entity “out there” who “infects” us, a passive victim? It’s fundamentally non-sensical, given these findings. It also clearly undermines the incessant, fear-based rhetoric those beholden to the pro-vaccine stance to coerce the masses into undergoing the largely faith-based rite of vaccination.
Let’s dive deeper into the study’s findings.
The next line of the abstract addresses the fact we opened this article with: namely, that there is great complexity involved at the level of the profound variability in virion composition:
“However, the virions of many viruses are complex and pleomorphic, making them difficult to analyze in detail”
But this problem of the great variability in the virion composition of influenza is exactly why the study was conducted. They explain:
“Here we address this by identifying and quantifying viral proteins with mass spectrometry, producing a complete and quantifiable model of the hundreds of viral and host-encoded proteins that make up the pleomorphic virions of influenza virus. We show that a conserved influenza virion architecture, which includes substantial quantities of host proteins as well as the viral protein NSI, is elaborated with abundant host-dependent features. As a result, influenza virions produced by mammalian and avian hosts have distinct protein compositions.”
In other words, they found that the flu virus is as much comprised of biological material from the host the virus ‘infects,’ as the viral genetic material of the virus per se.
How then, do we differentiate influenza virus as fully “other”? Given that it would not exist without “self” proteins, or those of other host animals like birds (avian) or insects, this would be impossible to do with any intellectual honesty intact.
There’s also the significant problem presented by flu vaccine production. Presently, human flu vaccine antigen is produced via insects and chicken eggs. This means that the virus particles extracted from these hosts would contain foreign proteins, and would therefore produce different and/or unpredictable immunological responses in humans than would be expected from human influenza viral particles. One possibility is that the dozens of foreign proteins found within avian influenza could theoretically produce antigens in humans that cross-react with self-structures resulting in autoimmunity. Safety testing, presently, does not test for these cross reactions. Clearly, this discovery opens up a pandora’s box of potential problems that have never sufficiently been analyzed, since it was never understood until now that “influenza” is so thoroughly dependent upon a host for its transmissability and immunogenecity.
Are Flu Viruses Really “Hijacked” Exosomes?
Lastly, the study identified something even more amazing:
“Finally, we note that influenza virions share an underlying protein composition with exosomes, suggesting that influenza virions form by subverting micro vesicle” production.”
What these researchers are talking about is the discovery that virion particles share stunning similarities to naturally occurring virus-like particles produced by all living cells called exosomes. Exosomes, like many viruses (i.e. enveloped viruses) are enclosed in a membrane, and are within the 50-100 nanometer size range that viruses are (20-400 nm). They also contain biologically active molecules, such as proteins and lipids, as well as information-containing ones like RNAs — exactly, or very similar, to the types of contents you find in viral particles.
Watch this basic video on exosomes to get a primer:
In light of this post-Germ Theory perspective, viruses could be described as pieces of information in search of chromosomes; not inherently “bad,” but, in fact, essential for mediating the genotype/phenotype relationship within organisms, who must adapt to ever-shifting environmental conditions in real-time in order to survive; something the glacial pace of genetic changes within the primary nucleotide sequences of our DNA cannot do (for instance, it may take ~ 100,000 years for a protein-coding gene sequence to change versus seconds for a protein-coding gene’s expression to be altered via modulation via viral or exosomal RNAs).
This does not mean they are “all good”, either. Sometimes, given many conditions outside their control, their messages could present challenges or misinformation to the cells to which they are exposed, which could result in a “disease symptom.” These disease symptoms are often if not invariably attempts by the body to self-regulate and ultimately improve and heal itself.
In other words, the virion composition of viruses appears to be the byproduct of the cell’s normal exosome (also known as microvesicle) production machinery and trafficking, albeit being influenced by influenza DNA. And like exosomes, viruses may be a means of extracellular communication between cells, instead of simply a pathological disease entity. This could explain why an accumulating body of research on the role of the virome in human health indicates that so-called infectious agents, including viruses like measles, confer significant health benefits. [see: the Health Benefits of Measles and The Healing Power of Germs?].
Other researchers have come to similar discoveries about the relationship between exosomes and viruses, sometimes describing viral hijacking of exosome pathways as a “Trojan horse” hypothesis. HIV may provide such an example.
Concluding Remarks
The remarkably recent discovery of the host-dependent nature of the influenza virus’ virion composition is really just the tip of an intellectual iceberg that has yet to fully emerge into the light of day, but is already “sinking” ships; paradigm ships, if you will.
One such paradigm is that germs are enemy combatants, and that viruses serve no fundamental role in our health, and should be eradicated from the earth with drugs and vaccines, if possible.
This belief, however, is untenable. With the discovery of the indispensable role of the microbiome, and the subpopulation of viruses within it — the virome — we have entered into an entirely new, ecologically-based view of the body and its environs that are fundamentally inseparable. Ironically, the only thing that influenza may be capable of killing is germ theory itself.
For an in-depth exploration of this, watch the lecture below on the virome. I promise, if you do so, you will no longer be able to uphold germ theory as a monolithic truth any longer. You may even start to understand how we might consider some viruses “our friends,” and why we may need viruses far more than they need us.
When pondering the possible outcomes of this Fourth Turning, we tend to be drawn towards the negative, because a positive outcome seems so unlikely given the current animosity roiling the country. If you step back and realize all the hate and conflict is being engineered and coordinated by a ruling class of powerful rich men, then average Americans could organize a new paradigm that honors the original intent of the U.S. Constitution, allowing citizens the liberty and freedom to create voluntary associations based upon common interests at a local level.
The ruling oligarchs find this unacceptable, so this freedom must be wrested away from them by any means necessary. There is a civil war already underway, but only one side is fighting – the billionaire class who not only don’t want to relinquish some power, but want total control over every aspect of our lives. I believe this election will turn this one-sided silent war into a hot war.
Rather than wallowing in doom and the worst-case scenarios, we should be trying to figure out how to reorganize our nation going forward, after the billionaire oligarchs are defeated. As I was trying to go back in time to see when I wrote my first Fourth Turning article, I came across an article I wrote in 2010 – Brave New World 2010.
At the end of the article I noted the wisdom and practicality of Aldous Huxley’s advice on how to restructure our society, from his 1958 book Brave New World Revisited. This should be a template for restructuring our way of life if we want a sustainable future. I am not optimistic we have the fortitude, wisdom, courage and will to choose Huxley’s suggested path:
As recent history has repeatedly shown, the right to vote, by itself, is no guarantee of liberty. Therefore, if you wish to avoid dictatorship by referendum, break up modern society’s merely functional collectives into self-governing, voluntarily cooperating groups, capable of functioning outside the bureaucratic systems of Big Business and Big Government.
If you wish to avoid the spiritual impoverishment of individuals and whole societies, leave the metropolis and revive the small country community, or alternately humanize the metropolis by creating within its network of mechanical organization the urban equivalents of small country communities, in which individuals can meet and cooperate as complete persons, not as the mere embodiments of specialized functions.
Huxley’s prescription of re-humanizing our country and voluntarily choosing where we want to live and who we want to associate with in small enclaves is how many rural communities already function. We can either willingly choose this path peacefully, or we will be left with this as our only option after our modern world self-destructs during the violent cataclysm, following the crashing of our Ponzi scheme debt saturated economic system.
The American Empire is clearly in rapid decline and may not survive the trials and tribulations over the coming decade. The Fourth Turning is not a prophecy, but should be taken as a warning and call to action. Sitting this out and hoping for the best will not help achieve a positive outcome. Tragedy or triumph – the choices we make will matter. The climax of this Fourth Turning may be a few years off, but the battle for the soul of America begins on November 3.
“History offers no guarantees. Obviously, things could go horribly wrong – the possibilities ranging from a nuclear exchange to incurable plagues, from terrorist anarchy to high-tech dictatorship. We should not assume that Providence will always exempt our nation from the irreversible tragedies that have overtaken so many others: not just temporary hardship, but debasement and total ruin. Losing in the next Fourth Turning could mean something incomparably worse. It could mean a lasting defeat from which our national innocence – perhaps even our nation – might never recover.” – Strauss & Howe – The Fourth Turning
Times of crisis often, although not inevitably, lead to times of awakening.
The lack of inevitability is a function of the minds (and spirits/souls) of individuals and their inclination towards the light or the darkness.
The physical separation of people has the effect of isolating many in their own mind sets which can be a rabbit hole all of itself.
And then these group uprisings, many of which are questionable in terms of the participants, are a major distraction in the news which will further polarize the country.
These things are, after all, tools used by the Uber-PTB, and by that I am referring to the ones over those who feel themselves to be the Powers That Be, who are the pawns who merely arrange the pieces as they are instructed— they are the tools used to achieve the end they have in sight.
There is also the ET factor, which definitely plays into the process we now see unfolding, a factor that can mean the further control of the human population.
But the spiritual movement towards awakening is a force that is motivating many, and hopefully the group energetics of light that are moving upward will calm the waters and bring some clarity.
L.G.L.R., and A.F. both sent this article along (and a thank you to both), and I had to sit up and take notice, because this one hits close to home, so to speak. Like many people my age, I was vaccinated as a child with the polio vaccine. In fact, it was the only vaccine my parents ever consented to allow me to take.
But that was not until after they had both done a little ‘digging”. At the time – the late fifties and early sixties – polio was still a killer if not a major crippler. Pictures of unfortunate people in iron lungs were still in the newspapers, and the disease was never far from our minds. My parents, of course, were the children of the depression era, and remembered the stories of President Franklin Roosevelt and his struggle with the disease. Say what one will about his policies (and I have a lot to say about them, and very little of it is good), one certainly cannot fault the man for waging a courageous struggle against the disease, including forcing himself to stand and walk, probably in a great deal of pain, and certainly with a great deal of effort, to give those speeches in front of Congress, or to meet on British battleships with Prime Minister Churchill. When it came to me, there were two choices of a polio vaccine then: the Salk vaccine (the first one out of the gate), and the Sabin vaccine.
The Salk vaccine actually caused vaccine-induced polio in a number of cases, and quickly became controversial, in part, because it was being pushed by the US government and state and local governments (sound familiar?). THe reason for the paralysis? The pharmaceutical company that had been the source for the vaccine had not adequately de-activated the virus in the vaccine, and hence, many children were injected with the real thing (sound familiar?).
The other alternative was the Sabin vaccine, administered orally in a sugar cube, and first extensively tested in Mexico and the Soviet Union. Because of the mess caused by the Salk vaccine, the Sabin vaccine became the vaccine of choice, including for my parents after consultation with their, and my, doctor.
I mention all this, because in the article L.G.L.R. and A.F. both sent me, polio vaccines are again in the news, and are again apparently causing some havoc:
This really should be one of the biggest scandals in public health, but it’s given little attention – mainly because of the high-profile nature of the people and organisations involved.
The United Nations has been forced to admit that a major international vaccine initiative is actually causing the outbreak of the very disease it was supposed to wipe-out.
While international organisations like the World Health Organization (WHO) will regular boast about supposedly ‘eradicating polio’ with vaccines, the opposite seems to be the case. Their decades-long campaign to eradicate polio is now killing scores of innocent young people living in poor countries.
Now it seems that health officials are beginning to admit that their plan to stop ‘wild’ polio is backfiring, as scores children are being paralyzed a deadly strain of the pathogen derived from a live vaccine – causing a virulent of polio to spread. (All emphases in the original)
A live virus in a polio vaccine… again? Shades of the Salk vaccine episode. One would think that since the 1950s we’d have learned how to kill a virus before putting it into a vaccine (c0vid-19 vaccine enthusiasts, take note!), but apparently we can’t, at least, not with 100% efficiency.
But wait, there’s more:
This latest pharma-induced pandemic has broken out in the African countries of Chad and Sudan, and the culprit has been identified: a vaccine-derived polio virus type 2. Officials now fear this new dangerous strain could soon ‘jump continents,’ causing further deadly outbreaks around the world.
Shocking as it sounds, this Big Pharma debacle is not new. After spending some $16 billion over 30 years to eradicate polio, international health bodies have ‘accidentally’ reintroduced the disease to in Pakistan, Afghanistan, and also Iran, as the central Asia region was hit by a virulent strain of polio spawned by the corporate pharmaceutical vaccine distributed there. Also, in 2019, the government of Ethiopia ordered the destruction of 57,000 vials of type 2 oral polio vaccine (mOPV2) following a similar outbreak of vaccine-induced polio.
It’s important to note that the oral polio vaccine being pushed on to the African population by the Global Polio Eradication Initiative (GPEI), a consortium which is supported and funded by the Bill & Melinda Gates Foundation.
All of this should be a cause for concern, especially with western governments and transnational pharmaceutical giant all rushing to roll-out their new Gates-funded experimental coronavirus vaccine for the global population. (Italicized emphasis added)
The Baal and Malicious Gates Foundation? You don’t say! Would this be the same folks with unusual ties to some eugenicists in their background, and if that’s the case, is the selection of African tests subjects, in this case, children of poor people in Chad and the Sudan, perhaps not coincidental? Sorry about the digression, they were just a few thoughts and questions that popped into my mind. But another thing just popped into my mind. Is this the same Baal and Malicious Gates that India banned due to the less-than-healthy-results of some vaccine trials there? Gee… I wonder…
The bottom line here, however, is that the vaccination-polio-eradication program has backfired, for the vaccine designed to eradicate it – which, let us note, is being orally administered in the pictures, and therefore appears to be some sort of update to the Sabin vaccine – is actually introducing more virulent strains into the population. And that in turn might mean that the entire population is once again at risk of the disease, perhaps even including those who, like me, received a vaccine against it as a child.
Gee, thanks alot, Baal, and Malicious.
And lest that misses the point, the article puts it so simple that even a noodnik busybody billionaire can understand it:
This latest revelation from Africa should prompt media and health advocates to ask hard questions about the efficacy and safety of the much-hyped COVID ‘miracle’ vaccine.
If he were that sort of chap, Prince Charles would be within his rights to deliver a right royal ‘I told you so’.
For in the years since he was roundly mocked for saying he talked to plants – and that they ‘responded’ – evidence has grown that he may have been on to something.
And now it appears plants may be smarter than even the Prince of Wales thought.
According to researchers, plants can count, make decisions, recognise their relatives and even remember events.
For in the years since he was roundly mocked for saying he talked to plants – and that they ‘responded’ – evidence has grown that he may have been on to something. Pictured: Stock photo of houseplants on a window
According to researchers, plants can count, make decisions, recognise their relatives and even remember events. Pictured: A gardener pruning a Hibiscus Plant
And while they may not have a brain, they can learn in a similar way to humans and animals, say scientists.
Professor Umberto Castiello said: ‘Although the idea that plants may behave in a cognitive way may baffle the public, many of us are genuinely amazed by the complexity of plant responses.
‘Evidence is accumulating supporting notions that plants can communicate, remember, decide, and even count – all abilities that one would normally call cognitive if they were observed in animals.’
Professor Castiello said many studies show their cognitive abilities. One found Venus flytraps can ‘count’ the number of steps their prey made.
Scientists observed that the plant trapped prey only when an insect triggered it twice within 20 seconds. This means the plants can remember the first signal for a short time. The reason why plants need to ‘count’ the steps of its prey could be to avoid wasting energy by responding to random raindrops or windblown debris.
Another experiment showed the flowering plant Mimosa pudica can remember being dropped.
The plant was dropped from 6in 60 times in a row and by the end of the experiment it no longer folded its leaves in a defensive response as it realised being dropped from that height would not hurt.
‘The plant “realises” that being dropped is normal,’ Professor Castiello, from the University of Padua in Italy, wrote. ‘More astonishingly, this reflex lasts up to a month which demonstrates the acquisition and expression of a long-lasting memory.’
And shrubs can recognise their kin too as they release more chemicals when planted near their relatives which helps them stave off predators.
It is even thought plants can manipulate competitors when resources are scarce. Plants experiencing a lack of water can share this information with nearby shrubs by sending signals via their roots.
This prompts a nearby plant – its competitor – to start conserving water and this behaviour ultimately benefits both.
Professor Castiello concluded: ‘The question should no longer be if plants are cognitive organisms but how plants make use of their cognitive capacities.’
The Centers for Disease Control (CDC) this week released a report that shows the types of health conditions and contributing causes mentioned in conjunction with deaths involving coronavirus disease 2019 (COVID-19).
In the latest update, the CDC pointed out that only 6% of deaths related to COVID-19 listed COVID-19 as the only cause of death. The vast majority of patients that were listed as COVID-19 related deaths also suffered from serious comorbidities.
CDC
The CDC is reporting 167,558 COVID-19 related deaths in the United State as of August 28, 2020. Out of the 167,558 COVID-19 related deaths, only 10,053 (6%) mentioned COVID-19 as the only cause according to the CDC’s new numbers. The other 94% of the COVID-19 related deaths had comorbidities associated with those deaths.
“What’s in a name? That which we call a rose by any other name would smell as sweet.” ~ William Shakespeare
By Catherine Austin Fitts
I am not a scientist. I am not a doctor. I am not a biotech engineer. I am not an attorney. However, I read, listen, appreciate, and try to understand those who are.
I was an investment banker until politics made it impossible to continue to practice my art. I was trained as a portfolio strategist—so I map my world by watching the financial flows and allocation of resources. I was also trained as a conspiracy generator and foot soldier—conspiracies being the fundamental organizing principle of how things get done in our world. It was not until I left the establishment that I learned that those not in the club had been trained to disparage and avoid conspiracies—a clever trick that sabotages their efforts to gather power.
My response to living at war with agencies of the U.S. government for a time was to answer the questions of people who were sufficiently courageous and curious to solicit my opinion. Over many years, that response transformed into two businesses. One was The Solari Report, which continues to grow as a global intelligence network—we seek to help each other understand and navigate what is happening and contribute to positive outcomes. The other was serving as an investment advisor to individuals and families through Solari Investment Advisory Services. After ten years, I converted that business to doing an ESG screen. What those who use it want—that is not otherwise readily available in the retail market—is a screen that reflects knowledge of financial and political corruption. Tracking the metastasizing corruption is an art, not a science.
When you help a family with their finances, it is imperative to understand all their risk issues. Their financial success depends on successful mitigation of all the risks—whether financial or non-financial—that they encounter in their daily lives. Non-financial risks can have a major impact on the allocation of family resources, including attention, time, assets, and money.
Many of my clients and their children had been devastated and drained by health care failures and corruption—and the most common catalyst for this devastation was vaccine death and injury. After their lengthy and horrendous experiences with the health care establishment, they would invariably ask, “If the corruption is this bad in medicine, food, and health, what is going on in the financial world?” Chilled by the thought, they would search out a financial professional who was schooled in U.S. government and financial corruption. And they would find me.
The result of this flow of bright, educated people blessed with the resources to pay for my time was that, for ten years, I got quite an education about the disabilities and death inflicted on our children by what I now call “the great poisoning.” I had the opportunity to repeatedly price out the human damage to all concerned—not just the affected children but their parents, siblings, and future generations—mapping the financial costs of vaccine injury again and again and again. These cases were not as unusual as you might expect. Studies indicate that 54% of American children have one or more chronic diseases. Doctors who I trust tell me that number is actually much higher, as many children and their families cannot afford the care and testing necessary to properly diagnose what ails them.
One of the mothers featured in VAXXED—a must-watch documentary for any awake citizen, as is its sequel VAXXED II: The People’s Truth—estimated that a heavily autistic child would cost present value $5MM to raise and care for over a lifetime. When my clients who were grandparents insisted that they would not interfere with their children’s vaccine choices because it was “none of their business,” I would say, “Really? Who has the $5MM? You or your kids? When your kids need the $5MM to raise their vaccine-injured child, are you going to refuse them? You are the banker, and it is your money that is at risk here, so it is your business. Do you want to spend that $5MM on growing a strong family through the generations or on managing a disabled child who did not have to be disabled?” Often, that $5MM in expenditures also translates into divorce, depression, and lost opportunities for siblings.
My clients helped me find the best resources—books, documentaries, articles—on vaccines. You will find many of them linked or reviewed at The Solari Report, including in our Library.
Of all the questions that I had, the one that I spent the most time researching and thinking about was why. Why was the medical establishment intentionally poisoning generations of children? Many of the writers who researched and wrote about vaccine injury and death assumed it was an aberration—resulting from the orthodoxy of a medical establishment that could not face or deal with its mistakes and liabilities. That never made sense to me. Writings by Forrest Maready, Jon Rappoport, Dr. Suzanne Humphries and Arthur Firstenberg have helped me understand the role of vaccines in the con man trick of saving money for insurance companies and the legally liable.
Here is one example of how the trick may play out. A toxin creates a disease. The toxin might be pesticides or industrial pollution or wireless technology radiation. The toxin damages millions of people and their communities. Companies or their insurance provider may be liable for civil or criminal violations. Then a virus is blamed. A “cure” is found in a “vaccine.” The pesticide or other toxic exposure is halted just as the vaccine is introduced, and presto, the sickness goes away. The vaccine is declared a success, and the inventor is declared a hero. A potential financial catastrophe has been converted to a profit, including for investors and pension funds. As a portfolio strategist, I admit it has been a brilliant trick and likely has protected the insurance industry from the bankrupting losses it would experience if it had to fairly compensate the people and families destroyed.
Thanks to the work of Robert Kennedy and Mary Holland of Children’s Health Defense, I now understand the enormous profits generated by so-called “vaccines” subsequent to the passage of the National Childhood Vaccine Injury Act of 1986 and the creation of the National Vaccine Injury Compensation Program—a federal no-fault mechanism for compensating vaccine-related injuries or deaths by establishing a claim procedure involving the United States Court of Federal Claims and special masters. Call a drug or biotech cocktail a “vaccine,” and pharmaceutical and biotech companies are free from any liabilities—the taxpayer pays. Unfortunately, this system has become an open invitation to make billions from “injectibles,” particularly where government regulations and laws can be used to create a guaranteed market through mandates. As government agencies and legislators as well as the corporate media have developed various schemes to participate in the billions of profits, significant conflicts of interest have resulted.
The Public Readiness and Emergency Preparedness Act (PREPA or the PREP Act) became law in 2005, adding to corporate freedoms from liability. The Act “is a controversial tort liability shield intended to protect vaccine manufacturers from financial risk in the event of a declared public health emergency. The act specifically affords to drug makers immunity from potential financial liability for clinical trials of . . . vaccine at the discretion of the Executive branch of government. PREPA strengthens and consolidates the oversight of litigation against pharmaceutical companies under the purview of the secretary of Health and Human Services.” (~ Wikipedia)
Over time, this has evolved to the engineering of epidemics—the medical version of false flags. In theory, these can be “psyops” or events engineered with chemical warfare, biowarfare, or wireless technology. If this sounds strange, dive into all the writings of the “Targeted Individuals.”
I learned about this first-hand when I was litigating with the Department of Justice and was experiencing significant physical harassment. I tried to hire several security firms; they would check my references and then decline the work, saying it was too dangerous. The last one took pity and warned me not to worry about electronic weaponry, letting me know that my main problem would be low-grade biowarfare. This biowarfare expert predicted that the opposing team would drill holes in the wall of my house and inject the “invisible enemy.” Sure enough, that is exactly what happened. I sold my house and left town. That journey began a long process of learning how poisoning and nonlethal weapons are used—whether to move people out of rent-controlled apartments, sicken the elderly to move them to more expensive government-subsidized housing, gangstalk political or business targets, or weaken or kill litigants—and the list goes on. Poisoning turned out to be a much more common tactic in the game of political and economic warfare in America than I had previously understood.
After I finished my litigation, I spent several years detoxing from heavy metal toxicity—including from lead, arsenic, and aluminum. As I drove around America, I realized it was not just me. Americans increasingly looked like a people struggling with high loads of heavy metals toxicity. In the process of significantly decreasing my unusually high levels of heavy metals, I learned what a difference the toxic load had made to my outlook, my energy, and my ability to handle complex information.
This brings me to the question of what exactly a vaccine is and what exactly is in the concoctions being injected into people today as well as the witches’ brews currently under development.
In 2017, Italian researchers reviewed the ingredients of 44 types of so-called “vaccines.” They discovered heavy metal debris and biological contamination in every human vaccine they tested. The researchers stated, “The quantity of foreign bodies detected and, in some cases, their unusual chemical compositions baffled us.” They then drew the obvious conclusion, namely, that because the micro- and nanocontaminants were “neither biocompatible nor biodegradable,” they were “biopersistent” and could cause inflammatory effects right away—or later (http://medcraveonline.com/IJVV/IJVV-04-00072.pdf)
Whatever the ingredients of vaccines have been to date, nothing is more bizarre and unsettling than the proposals of what might be included in them in the future. Strategies—already well-funded and well on the way—include brain-machine interface nanotechnology, digital identity tracking devices, and technology with an expiration date that can be managed and turned off remotely. One report indicates that the Danish government and U.S. Navy had been paying a tech company in Denmark to make an injectible chip that would be compatible with one of the leading cryptocurrencies.
I was recently reading Mary Holland’s excellent 2012 review of U.S. vaccine court decisions (“Compulsory vaccination, the Constitution, and the hepatitis B mandate for infants and young children,” Yale Journal of Health Policy, Law, and Ethics) and I froze and thought, “Why are we calling the injectibles that Bill Gates and his colleagues are promoting ‘vaccines’? Are they really vaccines?”
Most people are familiar with how Bill Gates made and kept his fortune. He acquired an operating system that was loaded into your computer. It was widely rumored that the U.S. intelligence agencies had a back door. The simultaneous and sudden explosion of computer viruses then made it necessary to regularly update your operating system, allowing Gates and his associates to regularly add whatever they wanted into your software. One of my more knowledgeable software developers once said to me in the 1990s—when Microsoft really took off—”Microsoft makes really sh***y software.” But of course, the software was not really their business. Their business was accessing and aggregating all of your data. Surveillance capitalism was underway.
The Department of Justice launched an antitrust case against Microsoft in 1998, just as the $21 trillion started to disappear from the U.S. government—no doubt with the help of specially designed software and IT systems. During the settlement negotiations that permitted Gates to keep his fortune, he started the Gates Foundation and his new philanthropy career. I laughed the other day when my tweet of one of Robert Kennedy Jr.’s articles from Children’s Health Defense—describing the gruesome technology Gates is hoping to roll out through “injectibles”—inspired a response: “Well, I guess he is finally fulfilling his side of his antitrust settlement.”
If you look at what is being created and proposed in the way of injectibles, it looks to me like these technological developments are organized around several potential goals.
The first and most important goal is the replacement of the existing U.S. dollar currency system used by the general population with a digital transaction system that can be combined with digital identification and tracking. The goal is to end currencies as we know them and replace them with an embedded credit card system that can be integrated with various forms of control, potentially including mind control. “De-dollarization” is threatening the dollar global reserve system. The M1 and M2 money supply have increased in the double digits over the last year as a result of a new round of quantitative easing by the Fed. The reason we have not entered into hyperinflation is because of the dramatic drop in money velocity occasioned by converting Covid-19 into an engineered shutdown of significant economic activity and the bankrupting of millions of small and medium-sized businesses. The managers of the dollar system are under urgent pressure to use new technology to centralize economic flows and preserve their control of the financial system.
Just as Gates installed an operating system in our computers, now the vision is to install an operating system in our bodies and use “viruses” to mandate an initial installation followed by regular updates.
Now I appreciate why Gates and his colleagues want to call these technologies “vaccines.” If they can persuade the body politic that injectible credit cards or injectible surveillance trackers or injectable brain-machine interface nanotechnologies are “vaccines,” then they can enjoy the protection of a century or more of legal decisions and laws that support their efforts to mandate what they want to do. As well, they can insist that U.S. taxpayers fund, through the National Vaccine Injury Compensation Program, the damages for which they would otherwise be liable as a result of their experiments—and violations of the Nuremberg Code and numerous civil and criminal laws—on the general population. The scheme is quite clever. Get the general population to go along with defining their new injectible high-tech concoctions as “vaccines,” and they can slip them right into the vaccine pipeline. No need to worry about the disease and death that will result from something this unnatural delivered this quickly. The freedom from liability guaranteed by the PREP Act through the declaration of an emergency—and the ability to keep the emergency going through contact tracing—can protect them from liability for thousands if not millions of deaths and disabilities likely to follow such human experimentation. Ideally, they can just blame the deaths on a virus.
A colleague once told me how Webster’s Dictionary came about. Webster said that the way the evildoers would change the Constitution was not by amending it but by changing the definitions—a legal sneak attack.
I believe that Gates and the pharma and biotech industries are literally reaching to create a global control grid by installing digital interface components and hooking us up to Microsoft’s new $10 billion JEDI cloud at the Department of Defense as well as Amazon’s multibillion cloud contract for the CIA that is shared with all U.S. intelligence agencies. Why do you think President Trump has the military organizing to stockpile syringes for vaccines? It is likely because the military is installing the roaming operating system for integration into their cloud. Remember—the winner in the AI superpower race is the AI system with access to the most data. Accessing your body and my body on a 24/7 basis generates a lot of data. If the Chinese do it, the Americans will want to do it, too. In fact, the rollout of human “operating systems” may be one of the reasons why the competition around Huawei and 5G telecommunications has become so fractious. As Frank Clegg, former President of Microsoft Canada has warned us, 5G was developed by the Israelis for crowd control.
In the face of global “de-dollarization,” this is how the dollar syndicate can assert the central control it needs to maintain and extend its global reserve currency financial power. This includes protecting its leadership from the civil and criminal liability related to explosive levels of financial and health care fraud in recent decades.
Which brings me back to you and me. Why are we calling these formulations “vaccines”? If I understand the history of case law, vaccines, in legal terms, are medicine. Intentional heavy metal poisoning is not medicine. Injectible surveillance components are not medicine. Injectible credit cards are not medicine. An injectible brain-machine interface is not a medicine. Legal and financial immunity for insurance companies does not create human immunity from disease.
We need to stop allowing these concoctions to be referred to by a word that the courts and the general population define and treat as medicine and protect from legal and financial liability.
The perpetrators of this fraud are trying a very neat trick—one that will help them go much faster and cancel out a lot of risk—at our expense. I understand why they are doing it.
What I don’t understand is why we are helping them. Why are we acquiescing in calling these bizarre and deeply dangerous concoctions “vaccines”? Whatever they are, they are not medicine.
So, what shall our naming convention be? What name shall we give to the relevant poisons, neurologically damaging metals, and digital shackles?
Whatever we call them, I know one thing. THEY ARE NOT MEDICINE, WHICH MEANS THEY SURE ARE NOT VACCINES.
