The Great Reset and Transhumanism Movement

The COVID pandemic has ushered in a new era of biodigital convergence — one that’s been in the works for decades but is now accelerating in the name of public health and new normalcy. As I said June 7, 2021, the most freedom in this new era will be awarded to those who are vaccinated.1 Speaking with The Andrew Narr Show, Tony Blair, former prime minister of Great Britain and Northern Ireland, affirmed this, stating, “It’s important to distinguish between the vaccinated and the unvaccinated. Giving the vaccinated the most amount of freedoms.”2 Freedom, however, isn’t something to be granted to you by authorities in exchange for obedience, but in this altered reality segregation between the vaccinated and unvaccinated is increasing. Those who comply will earn their freedom back, setting the mindset that by getting vaccinated and going along with government’s industrial process you’re being enhanced, while if you do not you’re holding society back, are noncompliant and may be a threat to others. As James Corbett covers in The Corbett Report above, we’re in the midst of:3 “… the implementation of a medical martial law system presided over by unappointed, unelected, unaccountable public health authorities who now have literal control over your everyday movements, who are constructing a total surveillance grid that comes with it the prospect of not just vaccine passports but health passes generally, which will be used to restrict your ability to access public life and that you will be guilty until proven innocent of infection under this new paradigm that is being installed.” This is only the beginning. The next step isn’t only about freedom but synthetic enhancement that will redefine what it means to be human. In all likelihood, opting in to biodigital convergence will come with rewards while resisting or rejecting will come with penalties. ‘Your Guide to the Great Convergence’ I warned about the COVID pandemic ushering in the Great Reset and the Fourth Industrial Revolution, which has been in discussion since at least 20164 and “is characterized by a fusion of technologies that is blurring the lines between the physical, digital and biological spheres.” The long-term agenda is not about COVID-19 or even the implementation of a biosecurity state but, as noted by Corbett, will be used for the extinction of homo sapiens — the end of humanity as you know it. This isn’t conjecture. The notion of transhumanism is being actively researched and explored. In an article titled “Looking Forward to the End of Humanity,” The Wall Street Journal noted that COVID-19 “has spotlighted the promise and peril of ‘transhumanism,’ the idea of using technology to overcome sickness, aging and death.”5 It talks about the need for “technological protection” to protect our species from being wiped out from nuclear war, asteroid collision, a technological accident or a pandemic. The problem is that, in so doing, humans are no longer “human,” at least, not the way you think of them now. According to The Wall Street Journal:6 “Ultimately, however, the hope is that we won’t just use computers — we’ll become them. Today, cognitive scientists often compare the brain to hardware and the mind to the software that runs on it. But a software program is just information, and in principle there’s no reason why the information of consciousness has to be encoded in neurons. The Human Connectome Project, launched in 2009 by the National Institutes of Health, describes itself as ‘an ambitious effort to map the neural pathways that underlie human brain function.’ If those pathways could be completely mapped and translated into digital 0s and 1s, the data could be uploaded to a computer, where it could survive indefinitely.” The human/computer metaphor was also used in a 2017 TED talk by Dr. Tal Zaks, chief medical officer at Moderna, who referred to mRNA technology as “the software of life.”7 Moderna, which was founded on the concept of being able to modify human biological function through genetic engineering, went on to develop one of the mRNA COVID-19 vaccines being pushed in the mass vaccination campaign. The potentially permanent modification of humans is an existential threat to the human species, according to Corbett, yet hardly anyone is talking about it. ‘Exploring Biodigital Convergence’ To get an idea of what’s on the horizon, look no further than “Exploring Biodigital Convergence,” a terrifying report by Policy Horizons Canada, which explores in detail “what happens when biology and digital technology merge.”8 Policy Horizons Canada is a Canadian government organization, whose director general is Kristel Van der Elst, the former head of strategic foresight at the World Economic Forum (WEF).9 In the report’s Foreword, Van der Elst is very open that, in the coming years, biodigital technologies may become integrated into everyday life the way digital technologies are now. Sh

The Great Reset and Transhumanism Movement

The COVID pandemic has ushered in a new era of biodigital convergence — one that’s been in the works for decades but is now accelerating in the name of public health and new normalcy. As I said June 7, 2021, the most freedom in this new era will be awarded to those who are vaccinated.1

Speaking with The Andrew Narr Show, Tony Blair, former prime minister of Great Britain and Northern Ireland, affirmed this, stating, “It’s important to distinguish between the vaccinated and the unvaccinated. Giving the vaccinated the most amount of freedoms.”2

Freedom, however, isn’t something to be granted to you by authorities in exchange for obedience, but in this altered reality segregation between the vaccinated and unvaccinated is increasing.

Those who comply will earn their freedom back, setting the mindset that by getting vaccinated and going along with government’s industrial process you’re being enhanced, while if you do not you’re holding society back, are noncompliant and may be a threat to others. As James Corbett covers in The Corbett Report above, we’re in the midst of:3

“… the implementation of a medical martial law system presided over by unappointed, unelected, unaccountable public health authorities who now have literal control over your everyday movements, who are constructing a total surveillance grid that comes with it the prospect of not just vaccine passports but health passes generally, which will be used to restrict your ability to access public life and that you will be guilty until proven innocent of infection under this new paradigm that is being installed.”

This is only the beginning. The next step isn’t only about freedom but synthetic enhancement that will redefine what it means to be human. In all likelihood, opting in to biodigital convergence will come with rewards while resisting or rejecting will come with penalties.

‘Your Guide to the Great Convergence’

I warned about the COVID pandemic ushering in the Great Reset and the Fourth Industrial Revolution, which has been in discussion since at least 20164 and “is characterized by a fusion of technologies that is blurring the lines between the physical, digital and biological spheres.”

The long-term agenda is not about COVID-19 or even the implementation of a biosecurity state but, as noted by Corbett, will be used for the extinction of homo sapiens — the end of humanity as you know it.

This isn’t conjecture. The notion of transhumanism is being actively researched and explored. In an article titled “Looking Forward to the End of Humanity,” The Wall Street Journal noted that COVID-19 “has spotlighted the promise and peril of ‘transhumanism,’ the idea of using technology to overcome sickness, aging and death.”5

It talks about the need for “technological protection” to protect our species from being wiped out from nuclear war, asteroid collision, a technological accident or a pandemic. The problem is that, in so doing, humans are no longer “human,” at least, not the way you think of them now. According to The Wall Street Journal:6

“Ultimately, however, the hope is that we won’t just use computers — we’ll become them. Today, cognitive scientists often compare the brain to hardware and the mind to the software that runs on it. But a software program is just information, and in principle there’s no reason why the information of consciousness has to be encoded in neurons.

The Human Connectome Project, launched in 2009 by the National Institutes of Health, describes itself as ‘an ambitious effort to map the neural pathways that underlie human brain function.’ If those pathways could be completely mapped and translated into digital 0s and 1s, the data could be uploaded to a computer, where it could survive indefinitely.”

The human/computer metaphor was also used in a 2017 TED talk by Dr. Tal Zaks, chief medical officer at Moderna, who referred to mRNA technology as “the software of life.”7 Moderna, which was founded on the concept of being able to modify human biological function through genetic engineering, went on to develop one of the mRNA COVID-19 vaccines being pushed in the mass vaccination campaign.

The potentially permanent modification of humans is an existential threat to the human species, according to Corbett, yet hardly anyone is talking about it.

‘Exploring Biodigital Convergence’

To get an idea of what’s on the horizon, look no further than “Exploring Biodigital Convergence,” a terrifying report by Policy Horizons Canada, which explores in detail “what happens when biology and digital technology merge.”8 Policy Horizons Canada is a Canadian government organization, whose director general is Kristel Van der Elst, the former head of strategic foresight at the World Economic Forum (WEF).9

In the report’s Foreword, Van der Elst is very open that, in the coming years, biodigital technologies may become integrated into everyday life the way digital technologies are now. She states quite clearly that this will redefine what it means to be “human”: “More than a technological change, this biodigital convergence may transform the way we understand ourselves and cause us to redefine what we consider human or natural.”10

And there’s more. The report outlines ways in which biodigital convergence is emerging and developing new ways to:11

Change human beings’ bodies, minds and behaviors

Change or create other organisms

Alter ecosystems

Sense, store, process and transmit information

Manage biological innovation

Structure and manage production and supply chains

Blurring What Is Considered Natural, Digital or Engineered

In biodigital convergence, biological and digital entities become fully integrated, “creating new hybrid forms of life and technology, each functioning in the tangible world, often with heightened capabilities.”12 Policy Horizons Canada makes it sound like this is no big deal, since “robots with biological brains and biological bodies with digital brains already exist, as do human-computer and brain-machine interfaces.”

But they’re literally talking about “tapping into the nervous system and manipulating neurons” to add technology to organisms with the intent of altering “its function and purpose.”13 What could possibly go wrong? For just one example of how the use of tech can quickly backfire, eerie snippets from the World Economic Forum’s 2016 meeting detailed research underway to decode your thoughts, read your mind and even use your own thoughts against you in a court of law.14

Ultimately, the plan is for a coevolution of biological and digital technologies, such that, “There is also a blurring between what is considered natural or organic and what is digital, engineered, or synthetic.”15 The section of the report titled, “Good morning, biodigital” is perhaps most disturbing of all, as it outlines a possible glimpse into a future biodigital world. I suggest you read it in its entirety, but here’s a snippet:16

“While I’m brushing my teeth, Jamie, my personal AI, asks if I’d like a delivery drone to come pick up my daughter’s baby tooth, which fell out two days ago. The epigenetic markers in children’s teeth have to be analysed and catalogued on our family genetic blockchain in order to qualify for the open health rebate, so I need that done today.

I replace the smart sticker that monitors my blood chemistry, lymphatic system, and organ function in real time. It’s hard to imagine the costs and suffering that people must have endured before personalized preventative medicine became common.

Also, I’ll admit that it sounds gross, but it’s a good thing the municipality samples our fecal matter from the sewage pipes. It’s part of the platform to analyze data on nutritional diversity, gut bacteria, and antibiotic use, to aid with public health screening and fight antibiotic-resistant strains of bacterial infections.”

Genobility — Creating a Superior Class of People

Wearable technology and neurotechnology are upon us, with brain computer interfaces and electrodes in development that would neurologically enhance humans. Currently, such interfaces are aimed at people with disabilities, but likely would progress into other “enhancements,” like super intelligence or preferred physical traits.17

Already, preimplantation genetic diagnosis is used to identify embryos without genetic defects, with claims that it will soon be able to screen for embryos with the highest IQ.18CRISPR-Cas9 gene-editing technology has also been used to alter DNA in human embryos in a way that would eliminate or correct the genes causing certain inherited diseases.

Soon, however, such enhancements could lead to “genobility,” in which certain people have superior genes or transhuman traits and the benefits that go along with them, while the “less superior” humans, like the unvaccinated, are awarded fewer rights. X Prize noted:19

“The future of genetic engineering must be regulated in order to prevent what the ethicist Ron Green calls a ‘genobility’ — a class of people with superior genes, who can afford to have them.

While this might sound sci-fi, we already live in a society with huge discrepancies around healthcare, points out Green, as the cost of genome sequencing is falling, and therefore may become more accessible to more people, regulation in the fields of human enhancement becomes ever more critical.”

Engineers Are Actively Making This Happen

Again, Corbett points out that this isn’t speculation. Researchers, such as MIT’s Susan Hockfield, Ph.D., are actively constructing ways to make transhumanism happen. Hockfield wrote the book, “The Age of Living Machines,” in which she explains “the coming convergence of biology and engineering — and how it will change our world for the better.”20

Corbett also pointed to a Harvard Magazine article from 2011, in which the former chairman of the Harvard department of chemistry, nanoscience expert Charles Lieber, Ph.D, created a virus-sized transistor that could penetrate cell membranes due to its fatty “lipid layer.”21

Pfizer and Moderna are now using a lipid nanoparticle delivery system for their mRNA COVID-19 vaccines, bringing us full circle. Lieber, by the way, was arrested in early 2020 by federal agencies, suspected of illegal dealings with China.22 Pentagon scientists and Profusa have also developed a tiny biosensor that can be embedded under your skin to detect disease. Profusa said it intended to seek FDA approval for their tissue-integrating biosensor in 2021.23

It’s essential to be aware of the coming “Great Convergence” and its intent to usher in transhumanism and a “Nano-Bio-Info-Cogno Paradigm.” Researchers wrote in Postdigital Science and Education:24

“A central point of critique in the critical philosophy of convergence is the political economy of ‘post-biological technocracy’ and its tendency to ‘numb’ the biological self and creates a kind of digital obedience where Big Tech ‘platform ontologies’ know us better than we know ourselves.”

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Researcher: 'We Made a Big Mistake' on COVID-19 Vaccine

The more we learn about the COVID-19 vaccines, the worse they look. In a recent interview1 with Alex Pierson (above), Canadian immunologist and vaccine researcher Byram Bridle, Ph.D., dropped a shocking truth bomb that immediately went viral, despite being censored by Google. It also was featured in a “fact” check by The Poynter Institute’s Politifact,2 which pronounced Bridle’s findings as “false” after interviewing Dr. Drew Weissman,3 a UPenn scientist who is credited with helping to create the technology that enables the COVID mRNA vaccines to work. But, as you can see below, unlike Bridle, Politifact neglected to go beyond interviewing someone with such a huge stake in the vaccine’s success. In 2020, Bridle was awarded a $230,000 government grant for research on COVID vaccine development. As part of that research, he and a team of international scientists requested a Freedom of Information Act (FOIA) access to Pfizer’s biodistribution study from the Japanese regulatory agency. The research,4,5 previously unseen, demonstrates a huge problem with all COVID-19 vaccines. “We made a big mistake,” Bridle says. “We thought the spike protein was a great target antigen; we never knew the spike protein itself was a toxin and was a pathogenic protein. So, by vaccinating people we are inadvertently inoculating them with a toxin.” This toxin, Bridle notes, can cause cardiovascular damage and infertility — a claim echoed by researchers such as Stephanie Seneff, Ph.D., and Judy Mikovits, Ph.D., whom I’ve interviewed about these issues. Pfizer Omitted Industry-Standard Safety Studies What’s more, TrialSite News reports6 that Pfizer documents submitted to the European Medicines Agency [EMA] reveal the company “did not follow industry-standard quality management practices during preclinical toxicology studies … as key studies did not meet good laboratory practice (GLP).” Neither reproductive toxicity nor genotoxicity (DNA mutation) studies were performed, both of which are considered critical when developing a new drug or vaccine for human use. The problems now surfacing matter greatly, as they significantly alter the risk-benefit analysis underlying the vaccines’ emergency use authorization. As reported by TrialSite News:7 “Recently, there has been speculation regarding potential safety signals associated with COVID-19 mRNA vaccines. Many different unusual, prolonged, or delayed reactions have been reported, and often these are more pronounced after the second shot. Women have reported changes in menstruation after taking mRNA vaccines. Problems with blood clotting (coagulation) — which are also common during COVID-19 disease — are also reported. In the case of the Pfizer COVID mRNA vaccine, these newly revealed documents raise additional questions about both the genotoxicity and reproductive toxicity risks of this product. Standard studies designed to assess these risks were not performed in compliance with accepted empirical research standards. Furthermore, in key studies designed to test whether the vaccine remains near the injection site or travels throughout the body, Pfizer did not even use the commercial vaccine (BNT162b2) but instead relied on a ‘surrogate’ mRNA producing the luciferase protein. These new disclosures seem to indicate that the U.S. and other governments are conducting a massive vaccination program with an incompletely characterized experimental vaccine. It is certainly understandable why the vaccine was rushed into use as an experimental product under emergency use authority, but these new findings suggest that routine quality testing issues were overlooked in the rush to authorize use. People are now receiving injections with an mRNA gene therapy-based vaccine, which produces the SARS-CoV-2 spike protein in their cells, and the vaccine may be also delivering the mRNA and producing spike protein in unintended organs and tissues (which may include ovaries).” Toxic Spike Protein Enters Blood Circulation The assumption that vaccine developers have been working with is that the mRNA in the vaccines (or DNA in the case of Johnson & Johnson and AstraZeneca’s vaccines) would primarily remain in and around the vaccination site, i.e., your deltoid muscle, with a small amount draining into local lymph nodes.8 Pfizer’s data, however, show this isn’t the case at all. Using mRNA programmed to produce luciferase protein, as well as mRNA tagged with a radioactive label, Pfizer showed that the majority of the mRNA initially remain near the injection site, but within hours become widely distributed within the body.9 We have known for a long time that the spike protein is a pathogenic protein. It is a toxin. It can cause damage in our body if it gets into circulation. ~ Dr. Byram BridleThe mRNA enters your bloodstream and accumulates in a variety of organs, primarily your spleen, bone marrow, liver, adrenal glands and, in women, the ovaries. The spike protein al

Researcher: 'We Made a Big Mistake' on COVID-19 Vaccine

The more we learn about the COVID-19 vaccines, the worse they look. In a recent interview1 with Alex Pierson (above), Canadian immunologist and vaccine researcher Byram Bridle, Ph.D., dropped a shocking truth bomb that immediately went viral, despite being censored by Google.

It also was featured in a “fact” check by The Poynter Institute’s Politifact,2 which pronounced Bridle’s findings as “false” after interviewing Dr. Drew Weissman,3 a UPenn scientist who is credited with helping to create the technology that enables the COVID mRNA vaccines to work. But, as you can see below, unlike Bridle, Politifact neglected to go beyond interviewing someone with such a huge stake in the vaccine’s success.

In 2020, Bridle was awarded a $230,000 government grant for research on COVID vaccine development. As part of that research, he and a team of international scientists requested a Freedom of Information Act (FOIA) access to Pfizer’s biodistribution study from the Japanese regulatory agency. The research,4,5 previously unseen, demonstrates a huge problem with all COVID-19 vaccines.

“We made a big mistake,” Bridle says. “We thought the spike protein was a great target antigen; we never knew the spike protein itself was a toxin and was a pathogenic protein. So, by vaccinating people we are inadvertently inoculating them with a toxin.”

This toxin, Bridle notes, can cause cardiovascular damage and infertility — a claim echoed by researchers such as Stephanie Seneff, Ph.D., and Judy Mikovits, Ph.D., whom I’ve interviewed about these issues.

Pfizer Omitted Industry-Standard Safety Studies

What’s more, TrialSite News reports6 that Pfizer documents submitted to the European Medicines Agency [EMA] reveal the company “did not follow industry-standard quality management practices during preclinical toxicology studies … as key studies did not meet good laboratory practice (GLP).”

Neither reproductive toxicity nor genotoxicity (DNA mutation) studies were performed, both of which are considered critical when developing a new drug or vaccine for human use. The problems now surfacing matter greatly, as they significantly alter the risk-benefit analysis underlying the vaccines’ emergency use authorization. As reported by TrialSite News:7

“Recently, there has been speculation regarding potential safety signals associated with COVID-19 mRNA vaccines. Many different unusual, prolonged, or delayed reactions have been reported, and often these are more pronounced after the second shot.

Women have reported changes in menstruation after taking mRNA vaccines. Problems with blood clotting (coagulation) — which are also common during COVID-19 disease — are also reported. In the case of the Pfizer COVID mRNA vaccine, these newly revealed documents raise additional questions about both the genotoxicity and reproductive toxicity risks of this product.

Standard studies designed to assess these risks were not performed in compliance with accepted empirical research standards. Furthermore, in key studies designed to test whether the vaccine remains near the injection site or travels throughout the body, Pfizer did not even use the commercial vaccine (BNT162b2) but instead relied on a ‘surrogate’ mRNA producing the luciferase protein.

These new disclosures seem to indicate that the U.S. and other governments are conducting a massive vaccination program with an incompletely characterized experimental vaccine.

It is certainly understandable why the vaccine was rushed into use as an experimental product under emergency use authority, but these new findings suggest that routine quality testing issues were overlooked in the rush to authorize use.

People are now receiving injections with an mRNA gene therapy-based vaccine, which produces the SARS-CoV-2 spike protein in their cells, and the vaccine may be also delivering the mRNA and producing spike protein in unintended organs and tissues (which may include ovaries).”

Toxic Spike Protein Enters Blood Circulation

The assumption that vaccine developers have been working with is that the mRNA in the vaccines (or DNA in the case of Johnson & Johnson and AstraZeneca’s vaccines) would primarily remain in and around the vaccination site, i.e., your deltoid muscle, with a small amount draining into local lymph nodes.8

Pfizer’s data, however, show this isn’t the case at all. Using mRNA programmed to produce luciferase protein, as well as mRNA tagged with a radioactive label, Pfizer showed that the majority of the mRNA initially remain near the injection site, but within hours become widely distributed within the body.9

blood clots can occur as a result, and is expelled in breast milk.

This is a problem, because rather than instructing your muscle cells to produce the spike protein (the antigen that triggers antibody production), spike protein is actually being produced inside your blood vessel walls and various organs, where it can do a great deal of damage.

“It’s the first time ever scientists have been privy to seeing where these messenger RNA [mRNA] vaccines go after vaccination,” Bridle told Pierson.10

“Is it a safe assumption that it stays in the shoulder muscle? The short answer is: absolutely not. It’s very disconcerting … We have known for a long time that the spike protein is a pathogenic protein.

It is a toxin. It can cause damage in our body if it gets into circulation … The spike protein on its own is almost entirely responsible for the damage to the cardiovascular system, if it gets into circulation.”

The Spike Protein Is the Problem

Indeed, for many months, we’ve known that the worst symptoms of severe COVID-19, blood clotting problems in particular, are caused by the spike protein of the virus. As such, it seemed really risky to instruct the body’s cells to produce the very thing that causes severe problems.

Bridle cites research showing that laboratory animals injected with purified spike protein from SARS-CoV-2 straight into their bloodstream developed cardiovascular problems and brain damage.

Assuming that the spike protein would not enter into the circulatory system was a “grave mistake,” according to Bridle, who calls the Japanese data “clear-cut evidence” that the vaccine, and the spike protein produced by it, enters your bloodstream and accumulates in vital organs. Bridle also cites recent research showing the spike protein remained in the bloodstream of humans for 29 days.

Once in your blood circulation, the spike protein binds to platelet receptors and the cells that line your blood vessels. As explained by Bridle, when that happens, one of several things can occur:

  1. It can cause platelets to clump together — Platelets, aka thrombocytes, are specialized cells in your blood that stop bleeding. When there’s blood vessel damage, they clump together to form a blood clot. This is why we’ve been seeing clotting disorders associated with both COVID-19 and the vaccines
  2. It can cause abnormal bleeding
  3. In your heart, it can cause heart problems
  4. In your brain, it can cause neurological damage

Importantly, people who have been vaccinated against COVID-19 absolutely should not donate blood, seeing how the vaccine and the spike protein are both transferred. In fragile patients receiving the blood, the damage could be lethal.

Breastfeeding women also need to know that both the vaccine and the spike protein are being expelled in breast milk, and this could be lethal for their babies. You are not transferring antibodies. You are transferring the vaccine itself, as well as the spike protein, which could result in bleeding and/or blood clots in your child. All of this also suggests that for individuals who are at low risk for COVID-19, children and teens in particular, the risks of these vaccines far outweigh the benefits.

The Spike Protein and Blood Clotting

In related news, Dr. Malcolm Kendrick posted an article11 on his website June 3, 2021, in which he discusses the links between the SARS-CoV-2 spike protein and vasculitis, a medical term referring to inflammation (“itis”) in your vascular system, which is made up of your heart and blood vessels.

There are many different types of vasculitis, including Kawasaki’s disease, antiphospholipid syndrome, rheumatoid arthritis, scleroderma and Sjogren’s disease. According to Kendrick, all of them have two things in common:12

1. Your body for some reason starts to attack the lining of your blood vessels, thereby causing damage and inflammation — The “why” can differ from one case to another, but in all cases, your immune system identifies something foreign in the lining of the blood vessel, causing it to attack. The attack causes damage to the lining, which results in inflammation.

Blood clots are a common result, and can occur either because the platelets clump together in response to the vessel wall damage, or because your anticlotting mechanism has been compromised. Your most powerful anticlotting system is your glycocalyx, the protective layer of glycoproteins that lines your blood vessels.

Among many other things, the glycocalyx contains a wide variety of anticoagulant factors, including tissue factor inhibitor, protein C, nitric oxide and antithrombin. It also modulates the adhesion of platelets to the endothelium. When blood clots completely block a blood vessel, you end up with a stroke or a heart attack.

A reduction in platelet count, known as thrombocytopenia, is a reliable sign that blood clots are forming in your system, as the platelets are being used up in the process. Thrombocytopenia is a commonly-reported side effect of COVID-19 vaccines, as are blood clots, strokes and lethal heart attacks — all of which are pointing toward spike proteins causing vascular damage.

2. They significantly increase your risk of death, in some cases raising mortality by 50 times compared to people who do not have these conditions.

The take-home message Kendrick delivers is that “If you damage the lining of blood vessel walls, blood clots are far more likely to form. Very often, the damage is caused by the immune system going on the attack, damaging blood vessel walls, and removing several of the anti-clotting mechanisms.” The end result can be lethal, and this chain of events is exactly what these COVID-19 vaccines are setting into motion.

SARS-CoV-2 Spike Protein May Damage Mitochondrial Function

Other research suggests the SARS-CoV-2 spike protein can have a serious impact on your mitochondrial function, which is imperative for good health, innate immunity and disease prevention of all kinds.

When the spike protein interacts with the ACE2 receptor, it can disrupt mitochondrial signaling, thereby inducing the production of reactive oxygen species and oxidative stress. If the damage is serious enough, uncontrolled cell death can occur, which in turn leaks mitochondrial DNA (mtDNA) into your bloodstream.13

Aside from being detected in cases involving acute tissue injury, heart attack and sepsis, freely circulating mtDNA has also been shown to contribute to a number of chronic diseases, including systemic inflammatory response syndrome or SIRS, heart disease, liver failure, HIV infection, rheumatoid arthritis and certain cancers.14 As explained in “COVID-19: A Mitochondrial Perspective”:15

“Apart from its role in energy production, mitochondria are crucial for … innate immunity, reactive oxygen species (ROS) generation, and apoptosis; all of these are important in COVID-19 pathogenesis. Dysfunctional mitochondria predispose to oxidative stress and loss of cellular function and vitality. In addition, mitochondrial damage leads to … inappropriate and persistent inflammation.

SARS coronavirus 2 (SARS-CoV-2) … enters cell by attaching to angiotensin converting enzyme 2 (ACE2) receptors on cell surface … Following infection, there is internalization and downregulation of ACE2 receptors.

At vascular endothelium, ACE2 performs conversion of angiotensin II to angiotensin (1–7). Thus, a low ACE2 activity subsequent to SARS-CoV-2 infection leads to imbalance in renin-angiotensin system with relative excess of angiotensin II.

Angiotensin II through binding to its type 1 receptors exerts pro-inflammatory, vasoconstrictive, and prothrombotic effects, while angiotensin (1–7) has opposing effects … In addition, angiotensin II increases cytoplasmic and mitochondrial ROS generation leading to oxidative stress.

Increased oxidative stress may lead to endothelial dysfunction and aggravate systemic and local inflammation, thus contributing to acute lung injury, cytokine storm, and thrombosis seen in severe COVID-19 illness …

A recent algorithm showed that majority of SARS-CoV-2 genomic and structural RNAs are targeted for mitochondrial matrix. Thus it appears that SARS-CoV-2 hijacks mitochondrial machinery for its own benefit, including DMV biogenesis. Manipulation of mitochondria by virus may lead to mitochondrial dysfunction and increased oxidative stress ultimately leading to loss of mitochondrial integrity and cell death …

Mitochondrial fission enables removal of the damaged portion of a mitochondrion to be cleared by mitophagy (a special form of autophagy). Metabolomic studies suggest that SARS-CoV-2 inhibits mitophagy. Thus, there is accumulation of damaged and dysfunctional mitochondria. This not only leads to impaired MAVS [mitochondrial antiviral signaling] response but also aggravates inflammation and cell death.”

The author, Pankaj Prasun, points out that the virus’ impact on mitochondria helps explain why COVID-19 is so much deadlier for older people, the obese, and those with diabetes, high blood pressure and heart disease.

All of these risk factors have something in common: They’re all associated with mitochondrial dysfunction. If your mitochondria are already dysfunctional, the SARS-CoV-2 virus can more easily knock out more mitochondria, resulting in severe illness and death.

The Spike Protein Is a Bioweapon

In my interview with Seneff and Mikovits (see earlier hyperlink), they both stressed that the key danger — both in COVID-19 and with the vaccines — is the spike protein itself. However, while the spike protein found in the virus is bad, the spike protein your body produces in response to the vaccine is far worse. Why?

Because the synthetic mRNA in the vaccine has been programmed to instruct your cells to produce an unnatural, genetically engineered spike protein. Specific alterations make it far more toxic than that found on the virus itself. Mikovits goes so far as to call the spike protein a bioweapon, as it is a disease-causing agent that demolishes innate immunity and exhausts your natural killer (NK) cells’ ability to determine which cells are infected and which aren’t.

In short, when you get the COVID-19 vaccine, you are being injected with an agent that instructs your body to produce the bioweapon in its own cells. This is about as diabolical as it gets.

In her paper, “Worse Than The Disease: Reviewing Some Possible Unintended Consequences of mRNA Vaccines Against COVID-19,” published in the International Journal of Vaccine Theory, Practice and Research in collaboration with Dr. Greg Nigh,16 Seneff explains why the unnatural spike protein is so problematic.

In summary, normally, the spike protein on a virus will collapse on itself and fall into the cell once it attaches to the ACE2 receptor. The vaccine-induced spike protein does not do this. Instead it stays open and remains attached to the ACE2 receptor, thereby disabling it and causing a host of problems that lead to heart, lung and immune impairment.

What’s more, because the RNA code has been enriched with extra guanines (Gs) and cytosines (Cs), and configured as if it’s a human messenger RNA molecule ready to make protein by adding a polyA tail, the spike protein’s RNA sequence in the vaccine looks as if it is part bacteria,17 part human18 and part viral at the same time.

There’s also evidence suggesting the SARS-CoV-2 spike protein may be a prion, which is yet another piece of really bad news, particularly as it pertains to vaccine-induced spike protein. Prions are membrane proteins and when they misfold, they form crystals in the cytoplasm resulting in prion disease.

Since the mRNA in the vaccines has been modified to spew out very high amounts of spike protein (far greater than that of the actual virus), the risk of excessive buildup in the cytoplasm is high. And, since the spike protein doesn’t enter into the membrane of the cell, there’s a high risk that it can become problematic if indeed it works like a prion.

Remember, the research cited by Bridle at the beginning of this article found the spike protein accumulates in the spleen, among other places. Parkinson’s disease is a prion disease that has been traced back to prions originating in the spleen, that then travel up to the brain via the vagus nerve. In the same way, it’s quite possible COVID-19 vaccines may promote Parkinson’s and other human prion diseases such as Alzheimer’s.

What Are the Solutions?

While all of this is highly problematic, there is help. As noted by Mikovits, remedies to the maladies that might develop post-vaccination include:

Hydroxychloroquine and ivermectin treatments. Ivermectin appears particularly promising as it actually binds to the spike protein. Please listen to the interview that Brett Weinstein did with Dr. Pierre Kory,19 one of Dr. Paul Marik’s collaborators

Low-dose antiretroviral therapy to reeducate your immune system

Low-dose interferons such as Paximune, developed by interferon researcher Dr. Joe Cummins, to stimulate your immune system

Peptide T (an HIV entry inhibitor derived from the HIV envelope protein gp120; it blocks binding and infection of viruses that use the CCR5 receptor to infect cells)

Cannabis, to strengthen Type I interferon pathways

Dimethylglycine or betaine (trimethylglycine) to enhance methylation, thereby suppressing latent viruses

Silymarin or milk thistle to help cleanse your liver

From my perspective, I believe the best thing you can do is to build your innate immune system. To do that, you need to become metabolically flexible and optimize your diet. You’ll also want to make sure your vitamin D level is optimized to between 60 ng/mL and 80 ng/mL (100 nmol/L to 150 nmol/L), ideally through sensible sun exposure. Sunlight also has other benefits besides making vitamin D.

Use time-restricted eating and eat all your meals for the day within a six- to eight-hour window. Avoid all vegetable oils and processed foods. Focus on certified-organic foods to minimize your glyphosate exposure, and include plenty of sulfur-rich foods to keep your mitochondria and lysosomes healthy. Both are important for the clearing of cellular debris, including these spike proteins. You can also boost your sulfate by taking Epsom salt baths.

To combat the toxicity of the spike protein, you’ll want to optimize autophagy, which may help digest and remove the spike proteins. Time-restricted eating will upregulate autophagy, while sauna therapy, which upregulates heat shock proteins, will help refold misfolded proteins and also tag damaged proteins and target them for removal. It is important that your sauna is hot enough (around 170 degrees Fahrenheit) and does not have high magnetic or electric fields.

Source : Mercola More   

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