Taking Back Our Stolen History
Covid Vaccine
Covid Vaccine

Covid Vaccine

The Spike Protein Is a Bioweapon

Dr. Patrick Whelan who grasped the danger of the spike protein before anyone else, gave his analysis in a letter he submitted to the FDA on December 8, 2020. Here’s an excerpt:

“I am concerned about the possibility that the new vaccines aimed at creating immunity against the SARS-CoV-2 spike protein have the potential to cause microvascular injury to the brain, heart, liver, and kidneys in a way that does not currently appear to be assessed in safety trials of these potential drugs.

… Meinhardt et al…. show that the spike protein in brain endothelial cells is associated with formation of microthrombi (clots)… In other words, viral proteins appear to cause tissue damage without actively replicating virus…. The Pfizer/BioNTech vaccine (BNT162b2) is composed of an mRNA that produces a membrane-anchored full-length spike protein. The mouse studies suggest that an untruncated form of the S1 protein like this may cause a microvasculopathy in tissues that express much ACE2 receptor.

…it appears that the viral spike protein… is also one of the key agents causing the damage to distant organs that may include the brain, heart, lung, and kidney. Before any of these vaccines are approved for widespread use in humans, it is important to assess in vaccinated subjects the effects of vaccination on the heart…. As important as it is to quickly arrest the spread of the virus by immunizing the population, it would be vastly worse if hundreds of millions of people were to suffer long-lasting or even permanent damage to their brain or heart microvasculature as a result of failing to appreciate in the short-term an unintended effect of full-length spike protein-based vaccines on these other organs. (“FDA shrugs off dire warning about lethal spike protein“, Truth in the Age of Covid)

From the very beginning, government regulators and their allies in public health establishment have ignored (or censored) the warnings of capable physicians and researchers. They also waved-off career immunologist and vaccinologist, Dr Byram Bridle who was the first in his profession to identify the spike protein as “a specific causative agent of disease”; aka–“a pathogen”. Here’s Bridle:

“‘We have known for a long time that the spike protein is pathogenic…. It is a toxin. It can cause damage in our body if it’s in circulation. Now, we have clear-cut evidence that . . . the vaccine itself, plus the protein, gets into blood circulation.’”

Once that happens, the spike protein can combine with receptors on blood platelets and with cells that line our blood vessels. This is why, paradoxically, it can cause both blood clotting and bleeding. ‘And of course the heart is involved, as part of the cardiovascular system… That’s why we’re seeing heart problems. The protein can also cross the blood-brain barrier and cause neurological damage.…

‘In short,… we made a big mistake. We didn’t realize it until now. We didn’t realize that by vaccinating people we are inadvertently inoculating them with a toxin.”… (“Vaccine scientist: ‘We’ve made a big mistake’“, Conservative Woman)

Here again, we have a highly-regarded immunologist, with more than 3 decades of experience under his belt, who offered his informed and evidence-based research on an issue that should have been of great interest to the regulators that were making decisions about the long-term safety of the experimental drug they were foisting on millions of people across the country. But there was no interest at all. Despite the fact that the science supported his conclusions, Bridle was viciously attacked, censored, dragged through the mud, and forced to leave his place of employment.

Why?

Because he drew the same conclusions as Dr. Patrick Whelan. There’s really no substantive difference between the two except that Bridle’s comments attracted more attention in the media which made him a greater threat to the “universal vaccination” strategy. That was his real crime; he discovered the truth and made his findings available to the public, basically alerting them to the dangers of the “poison-death shot”. For that he was crushed.

Bridle has since made other claims that should concern anyone whose cancer might be in remission. Here’s what he said in a recent interview:

“What I’ve seen way too much of is people who had cancers that were in remission, or that were being well controlled; their cancers have gone completely out of control after getting this vaccine. And we know the vaccine causes a drop in T-cell numbers, and those T-cells are part of our immune system and they are part of the critical weapons our immune system has to fight off cancer cells; so there’s a potential mechanism there. All I can say, is I’ve had way too many people contact me with these reports for me to feel comfortable. I would say that is my newest major safety concern, and it’s also the one that’s going to be the most under-reported in the adverse data base, because if someone has had cancer before the vaccine, there’s no way public health officials will ever link it to the vaccine.” (“Dr Byram Bridle speaks”, Bitchute, :55 second-mark)

So, the vaccine suppresses the immune system? Yes, it does, and author Alex Berenson provided evidence of this just recently in an article he posted on Substack. Here’s an excerpt:

“… the British government…. admitted today, in its newest vaccine surveillance report, that:

“N antibody levels appear to be lower in people who acquire infection following two doses of vaccination.” (Page 23)

What’s this mean?…

What the British are saying is they are now finding the vaccine interferes with your body’s innate ability after infection to produce antibodies against not just the spike protein but other pieces of the virus….

This means vaccinated people will be far more vulnerable to mutations in the spike protein EVEN AFTER THEY HAVE BEEN INFECTED AND RECOVERED ONCE…

… it probably is still more evidence the vaccines may interfere with the development of robust long-term immunity post-infection.” (“URGENT: Covid vaccines will keep you from acquiring full immunity EVEN IF YOU ARE INFECTED AND RECOVER”, Alex Berenson, Substack)

Berenson’s observations square with research that was compiled earlier in the year by scientists in The Netherlands and Germany who:

“….warned that the … (COVID-19) vaccine induces complex reprogramming of innate immune responses that should be considered in the development and use of mRNA-based vaccines… the research team from Radboud University Medical Center and Erasmus MC in the Netherlands… showed that the vaccine altered the production of inflammatory cytokines by innate immune cells following stimulation with both specific (SARS-CoV-2) and non-specific stimuli.

Following vaccination, innate immune cells had a reduced response to toll-like receptor 4 (TLR4), TLR7 and TLR8 – all ligands that play an important role in the immune response to viral infection…. an unexplored area is whether BNT162b2 vaccination has long-term effects on innate immune responses …

This could be very relevant in COVID-19, in which dysregulated inflammation plays an important role in the pathogenesis and severity of the disease,” writes the team. “Multiple studies have shown that long-term innate immune responses can be either increased (trained immunity) or down-regulated (innate immune tolerance) after certain vaccines or infections.” (Research suggests Pfizer-BioNTech COVID-19 vaccine reprograms innate immune responses, new-medical-net)

Berenson’s finding also align with with cutting-edge research showing that the spike protein greatly “impedes adaptive immunity” by preventing DNA from repairing damaged cells. The paper suggests that the spike protein does in fact “impact on the nucleus of the cell, where we store our DNA, our core genetic material.” Here’s more from Berenson’s breakdown of the paper:

“…. our cells have mechanisms to repair their own DNA.

But – at least in the experiments these two scientists ran – the spike protein appeared to interfere with our own DNA repair proteins: “Mechanistically, we found that the spike protein localizes in the nucleus and inhibits DNA damage repair by impeding key DNA repair protein BRCA1 and 53BP1 recruitment to the damage site.”

To be clear, the scientists did NOT prove the spike protein was causing these problems in people, or even animals… Nonetheless, at a time when advanced countries that have high mRNA (and DNA/AAV) vaccination rates are seeing unusually full hospitals and higher-than-normal death rates, they are yet more cause for concern. As the authors explained:
“Our findings reveal a potential molecular mechanism by which the spike protein might impede adaptive immunity and underscore the potential side effects of full-length spike-based vaccines.” (“URGENT: Worrisome paper about the spike protein’s impact on DNA and DNA repair”, Alex Berenson, Substack)

Bottom line: If the vaccine does in fact inhibit the body’s innate immune response, then people are going to get alot sicker from seasonal infections that routinely spread through the population. Their path to recovery will also be alot more difficult.

But rather that belabor the immunity angle, let’s move on to the research of Dr Charles Hoffe who was the first physician to provide hard evidence that the vaccines generate blood clots by triggering an immune response in which the body attacks the thin layer of cells lining the walls of the blood vessels. Hoffe found that 62% of his patients that had been vaccinated tested positive for blood clots on a D-dimer test. Naturally, he was alarmed by what he found, particularly since the vaccine “was causing serious neurological events, and even death. When he raised his concerns with the BC College of Physicians, they immediately implemented a gag order, and reprimanded him in an attempt to intimidate, and silence him.”

Hoffe has been interviewed a number of times and always provides a detailed and riveting account of his findings. In a recent interview, he predicted that some vaccinees suffering from clot-related issues would likely die in just three years. Here’s what he said:

“… once you block off a significant number of blood vessels to your lungs, your heart must pump at a much greater resistance to get the blood through your lungs. That causes a condition called pulmonary artery hypertension, which is high blood pressure in your lungs because so many of the blood vessels in your lungs are blocked. And the terrifying thing about this is tha t people with pulmonary artery hypertension usually die of right-sided heart failure in three years… And not only is the long-term outlook very grim, but with each successive shot, the damage will add and add and add. It’s going to be cumulative because you are getting more and more damaged capillaries.” (“Shock: Doctor Warns That Majority Of Vaccinated Patients Could HavePermanent Heart Damage, Some May Die Within Three Years”Permanent Heart Damage, Some May Die Within Three Years”, Infowars; Minute 6:10)

Once again, there is no discrepancy between the analysis of Whelan, Bridle and Hoffe. And while the focus of their attention might vary slightly, their conclusions are the same. These experimental injections pose serious risks for anyone who allows himself to be inoculated.

Now check out how similar Hoffe’s analysis is to Dr. Rochagne Kilian who was an Emergency Room physician at the GBHS hospital until she resigned in protest. This is a particularly important video as it describes the “oddball” symptoms and exceedingly rare conditions that are now presenting in emergency rooms everywhere following the mass vaccination of millions of people with the “poison-death shot”. (I transcribed the video myself, so there could be errors.)

Dr Rochagné Kilian – Blows the Whistle on Covid-19 Vaccines and D-Dimer Levels

“What I was seeing in my ER department especially in the last 8 to 9 months is related to the D-Dimer levels. We use D-Dimers specifically related to pulmonary embolisms as well as Deep Vein Thrombosis. D-Dimer detects any thrombosis (clots) in the body but it doesn’t give you a diagnosis it gives you a basis for going further and doing an ultrasound and CT scan to either confirm or deny the presence of a pulmonary embolism or Deep Vein Thrombosis.

The first part of 2020 was probably the slowest ever in the emergency department, but when we went into 2021 and the vaccination rollout started, we ended up seeing an increase in stroke, transient ischemic attacks and stroke like presentations. (There were) definitely significant larger numbers of those people coming in. I ended up doing D-dimer tests on these people and never before in my clinical experience had I seen D-dimers and the amount of people with positive D-dimers higher than 2,000, higher than 3,000 and higher than 5,000. My clinical experience told me a needed to go look for a large clot either in their legs or their lungs. And I ended up doing a CT scan on these people. Most of them, and I will say almost all of them, had negative scans which started making me think that if there was not a significant clot in their lungs, but my D-dimer was so much higher than what I was usually seeing, it might not be concentrated in one clot. But that it is multiple micro-thrombi extended throughout the body, and that is so easy to miss because the CT scan is not going to pick it up.

“These people coming into the ER were all people anywhere from about a week to four months after receiving their 2nd injections. There are certain factors that can influence a D-dimer test that can give you a sense of a higher level than would be expected in the body. That said, the patients I was doing D-Dimer tests on did not have a level of maybe a positive 500 or 400 reading. It was more than 3500, more than 5000 ng/ml. So those are significantly positive without any proof of having a pulmonary embolism. If I was seeing high levels of D-dimer without a definite diagnosis, I needed to ask more questions.

One study said, never ignore extremely elevated D-dimer levels. They are specific for serious illness, including venous thrombosis, sepsis, and/or cancer. Even if sharply elevated D-dimer are a seemingly solitary finding, clinical suspicion of severe underlying disease should be maintained.

There were two conditions that stood out and the first one was disseminated intravascular coagulation also known as DIC. The second one is antiphosphlipid syndrome. Both of these conditions are related to an abnormality in either the initiation or the feedback of the coagulation pathway as well as thrombosis or the thrombosis cycle where clots are being broken down. DIC is a serious sometimes life threatening situation in which the proteins in the blood involved in blood clotting become overactive. It’s a cascade that’s difficult to stop once it’s reached a certain level. There are certain conditions that trigger DIC; significant sepsis, underlying viruses, trauma, major surgery, pregnancy and childbirth. And less common causes toxic drug reaction, blood transfusion reaction, and organ transplants. So there was a connection with intravascular products and a possible DIC.

Most cases of DIC are diagnosed rapidly and suddenly which is the acute presentation. But there are cases where it develops gradually, occurring over a longer period of time. This is known as a chronic form of DIC and I would go as far to say a subacute form of DIC that is very easy to miss. Simultaneous clotting and bleeding can occur with chronic DIC. The bleeding part comes in blood in the urine, headaches and other symptoms associated with brain bleeds, bruising, inflammation of red, small dots on the limbs, bleeding at sites of wounds and mucosal bleeding. which means bleeding out of the gums and nose. I definitely saw an increase in nose bleeds and bleeding from previous wound sites. ulcers, as well as rashes that couldn’t be explained. Blood clotting symptoms and signs were symptoms like chest pains, heart attacks, strokes, TIAs, and headaches either related to bleeding or not. As well as symptoms related to kidney failure, because of the clotting of those smaller blood vessels that go to the kidneys. Antiphosphlipid syndrome is a very similar type of condition. But the basis of the antiphosphlipid syndrome is an autoimmune disorder meaning that the body’s immune system makes proteins–known as antibodies–that mistakenly attacks its own body or tissues. That gives the skin the cascading effect of clotting disorder but it is linked to an autoimmune trigger. Basically, it presented in exactly the same way; high blood pressure which I was seeing alot of; first diagnosis of high blood pressure, heart attacks, strokes, TIAs, heart valve problems, repeated headaches or migraines, vision loss, balance and mobility problems, difficulty concentrating or thinking clearly,

The astute listener would start forming a picture of what we’ve been told about Covid-19, and there are research papers connecting Covid 19 with an underlying vascular disease. One of these was a study called “Covid 19; unraveling the clinical progression of Nature’s Virtually perfect Biological weapon.”

“SARS-Cov-2, presenting as Covid-19 syndrome, was not a respiratory basis, but an underlying vascular basis. which had certain phases of incubation, pulmonary phase, pro inflammatory phase, (which once again comes into a cytotoxic inflammation process) then moves into a protothrombic phase . Covid-19 is a thrombotic disease. implications for prevention, antithrombotic therapy and follow up…..

This picture shows us certain risk factors, Homeostatic Abnormalities, as well as clinical outcomes. It indicates increased D-dimer levels. It also mentions Venous Thromboembolism, Myocardial Infarction, and Disseminated Intravascular Coagulation that is connected to postulated mechanisms of coagulathopy as well as parthenogenesis of thrombosis in Covid-19…

I started asking the question, if we are able to detect certain connections between vascular abnormalities and Covid-19, and we based our proposed treatment on the spike protein, which includes the Pfizer and Moderna injections, shouldn’t we be looking for similar side effects or complications from that same injection?

If we are mandating certain treatments, we do need to do the due diligence to make sure what the side effects and complications especially in a time where there has not been long term studies.”And that’s what led me to focusing on D-dimers.” (“Dr Rochagné Kilian – Blows the Whistle on Covid-19 Vaccines and D-Dimer Levels“, Bitchute)

Kilian’s statement should be read over and over again. It is the most detailed description we have of the mysterious and deeply sinister machinations of a laboratory-engineered bioweapon that, in effect, turns the vascular and immune systems against the person who was vaccinated. Disseminated intravascular coagulation and antiphosphlipid syndrome are names that are entirely unknown to the American people, and yet, these freakish conditions are now responsible for a growing number of patients that are experiencing bleeding, clotting, headaches, rashes, bruising, high blood pressure, and inflammation . And– in more extreme cases– chest pains, heart attacks, strokes, heart-valve problems, and brain bleeds. One can only guess how the media will try to cover-up these extraordinarily-rare and potentially life-threatening conditions??

When Kilian asks:

“If we are able to detect certain connections between vascular abnormalities and Covid-19… shouldn’t we be looking for similar side effects or complications from that same injection?”

Bingo! If the spike protein produced by the vaccines, inflicts the same internal damage as Covid-19, then shouldn’t doctors expect to see the same symptoms?

Yes, they should. And if the symptoms are the same, then there’s a good chance that vaccine-induced injuries are being misdiagnosed as Covid-19.

Think about that for a minute. That would be the perfect scenario for the pandemic managers and their billionaire backers who’d love to see the impending mountain of carnage blamed on the waning virus instead of on their own poison-death shot.

And that is the evil-genius of the globalist strategy; to remove the fingerprints from the smoking gun before the investigators even arrive at the scene of the crime.

The amount of planning that must have gone into this scam, is simply breathtaking.1

In an interview with Dr. Seneff and Dr. Mikovits, they both stressed to interviewer Dr. Mercola 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, 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, part human and part viral at the same time.

“The pathogen that is causing all the deaths from the illness is the spike protein. And the spike protein is what the vaccine is supposed to make in your body. …Spike protein is one of the most contrived poisons that man has ever made. And, the aim of this toxin, is to kill billions of people without anyone noticing it. So it is a poison with an agenda.” (“South African Physician Dr. Shankara Chetty Talks about “The Bigger Plan”, Bitchute)

There it is in a nutshell. And Chetty is not alone in linking the vaccine to the agenda of the globalist elites who plan to use the cover of a pandemic to implement their “population management” scheme. Former Pfizer vice president, Mike Yeadon, offered a similar view just days ago on his website. He said:

“We are in the midst of the biggest depopulation program the world has ever seen, where most of humanity are acting as useful idiots to it and to their own demise.”

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.

Systemic inflammation, auto-reactive antibodies and autoimmune problems are not insignificant concerns. In fact, these are in large part why previous attempts to create a coronavirus vaccine have ALL failed.

Over the past 20 years, coronavirus vaccine research has been plagued by one consistent adverse outcome in particular, namely paradoxical immune enhancement. This is caused by the fact that coronaviruses produce two different types of antibodies—neutralizing antibodies5 that fight the infection, and binding antibodies6 (also known as nonneutralizing antibodies) that cannot prevent viral infection.

Incapable of preventing viral infection, binding antibodies can instead trigger paradoxical immune enhancement. What that means is that it looks good until you get the disease, and then it makes the disease far worse than it would have been otherwise. As detailed in my interview with Robert F. Kennedy Jr., in one coronavirus vaccine trial using ferrets, all the vaccinated animals died when exposed to the actual virus.

According to Madej, animal studies have also found the type of mRNA technology introduced with this vaccine can increase the risk of cancer and mutagenesis (gene mutations).

Scientists have found the synthetic spike proteins in COVID vaccines are more dangerous than in naturally-occurring SARS-COV-2 infections to susceptible persons because:

  1. COVID-19 victims die from cytokine storms when the body’s immune system attacks the body’s organs.  Vaccines can cause antibody dependent enhancement (ADE), a quicker cytokine storm, i.e., more severe illness, when a vaccinated person is next exposed to a wild virus. Prior attempts to develop coronavirus vaccines killed test animals or made them severely ill when subsequently encountering the wild virus. ADE occurs more in elderly or high-risk persons, in persons who had previous influenza vaccines or previously recovered from a SARS-COV-2 infection. Informed consent requires disclosing ADE risk;
  2. mRNA and the vector COVID vaccines are “leaky ” i.e., do not stop infection or transmission.  In a Geert Bossche warned of deaths from mass corona vaccinations (Epoch Times March 2021) because leaky vaccines cause immune escape — the mutation and spread of more infectious viral variants.  In May, world-reknowned Nobel laureate virologist Luc Montagnier warned COVID vaccination is creating new variants. Vaccinated persons become spreaders of more infectious mutations of SARS-COV-2.  The more people vaccinated, the higher the risk of evolving strains.  There is evidence of vaccinated spreaders and an increase in serious COVID cases among the young, e.g. in Israel. “Break-through” cases are occurring in fully vaccinated people worldwide. E.g., Florida;
  3. The lipid nano-particles (LNP)s cause human cells to manufacture synthetic spike proteins throughout the body that are more pathogentic than the original SARS-COV-2 spike protein, quickly spreading in greater numbers inside the body than a natural infection; causing, often, a large bump in excess mortality concomidant with vaccination rollouts.  The spike protein may invade brain tissue, infecting neurons and causing neurotropism.  The S1 sub-unit of the spike protein enters the parenchymal tissue of the brain in murine models. The brain’s endothelial cells attempt to hide the spike protein in the brain capillary glycocalyx, which can lead to degradation of the glycocalyx, dysfunction of the blood-brain barrier (BBB) and cerebral edema. (citation);
  4. The polyethylene glycol, PEG, encasing the lipid nano-particles in the Pfizer mRNA vaccine, causes severe allergic reactions and anaphylaxis in some persons;
  5. Risks of blood coagulation and clotting (thrombosis) or Covid vaccine-induced immune thrombotic thrombocytopenia, or VITT is caused by synthetic spike proteins growing in the lungs, heart, ovaries, brain, liver, kidneys, bone marrow, testes, and other organs  disabling the body’s ACE-2 receptors…  The spike proteins bind to endothelial cells lining blood vessels. … causing platelets to clot in a majority of vaccine recipients… and may cause bleeding disorders …and heart problems. … and … cause neurological damage and clots in the brain. (citation). Doctors have reported seeing rapid development of advanced cancers occurring post-Covid vaccination in liver, lungs, and bones.
  6. The Covid mRNA and DNA vaccines do not provide mucosal immunity that  would prevent infection and spread of COVID disease.  (see Mucosal Immunity in COVID-19: A Neglected but Critical Aspect of SARS-CoV-2 Infection  by Michael W. Russell, Department of Microbiology and Immunology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, United States, Zina Moldoveanu, Pearay L. Ogra, Division of Infectious Diseases, Department of Pediatrics, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, United States and Jiri Mestecky, Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL, United States  30 November 2020 | https://doi.org/10.3389/fimmu.2020.611337 )   The mucosal immune system is the largest component of the human immune system, … providing protection at the main sites of infectious threat: the mucosael barriers. As SARS-CoV-2 initially infects the upper respiratory tract, its first interactions with the immune system is predominantly at respiratory mucosal surfaces…

Some doctors recommend isolating for up to 30 days after a COVID injection to avoid harming others while shedding pathogenic spike proteins; to avoid getting a SARS-COV-2 infection during first two weeks post-vaccination when the immune system is vulnerable; and, to take preventative measures.  See  COVID “vaccine” adverse events.

What Doctors & Scientists Are Saying

  • “We knew these vaccines would kill people.”
  • By lying about safe remedies like Ivermectin and hydroxychloroquine,, governments have committed “mass murder.”
  • “Don’t be afraid of COVID or ‘variants.’ Be terrified of your government.”
  • “These are not ‘slip-ups’, ‘well-intentioned mistakes’…They’re deliberately misleading.”

The COVID shot vs. Alternative Treatment. October 11, 2021. Dr. Zelenko is a board-certified family physician with over 20 years of experience. He is published in top peer reviewed journals with world renowned physicians. He’s the first in the world to develop therapeutics against COVID. He has been nominated for the Nobel Peace Prize and has been recognized as a hero at a Department of Homeland Security committee hearing.

Geert V. Bossche: Keep Asking the Wrong Questions and We’ll Never Tame this Pandemic  October 10, 2021.

Why are we vaccinating children against COVID-19? Oct 7, 2021. Ronald N.Kostoffa, Daniela Calinab, Darja Kanducc, Michael B.Briggs, Panayiotis Vlachoyiannopoulose, Andrey A. Svistunovf, Aristidis Tsatsakisg   https://doi.org/10.1016/j.toxrep.2021.08.010  A novel best-case scenario cost-benefit analysis showed very conservatively that there are five times the number of deaths attributable to each inoculation vs those attributable to COVID-19 in the most vulnerable 65+ demographic. The risk of death from COVID-19 decreases drastically as age decreases, and the longer-term effects of the inoculations on lower age groups will increase their risk-benefit ratio, perhaps substantially.

audio podcast: Covid Vaccine & Kids part 2: with Dr. Paul Alexander. October 7, 2021.

‘We’re in the middle of a major biological catastrophe’: COVID expert Dr. Peter McCullough. October 6, 2021. In a recent lecture, Dr. Peter McCullough presented alarming data related to COVID vaccines, the fraud of national health authorities, the ‘Therapeutic Nihilism’ being exercised in hospitals, and the urgent necessity of active resistance.    There is no data safety monitoring board (DSM) overseeing this COVID vaccine rollout.

The Oxford researchers reveal that 1 in 100 or 1% of all vaccinated individuals were admitted to the hospital or died with arrhythmia or irregular heartbeat.

Of the 38,615,491 vaccinated individuals included in our study, 385,508 (1.0%) were admitted to hospital with or died from cardiac arrhythmia at any time in the study period (either before or after vaccination); 86,754 (0.2%) of these occurred in the 1-28 days after any dose of vaccine. Of those who were admitted or died 39,897 (10.3%) had a SARS-CoV-2 positive test, with 29,694 (7.7%) having a positive test before vaccination. There were 7,795 deaths with cardiac arrhythmia recorded as the cause of death (1,108 had a SARS-CoV-2 positive test).

The unforgivable sin! G. Vanden Bossche, DVM, PhD October 2021 … “As the mechanism of immune defense in vaccinees is totally different from the one at play in unvaccinated individuals, the mantra of mass vaccination stakeholders that vaccination of youngsters and children will provide them with improved protection from contracting severe disease is a textbook example of scientific nonsense.

Their irrational, erroneous extrapolations lead people to believe that they should get their children vaccinated whereas there is barely any more catastrophic immune intervention one could think of.  …  healthy children and youngsters are NOT ‘naturally’ susceptible to any Sars-CoV-2 lineage but exclusively acquire such susceptibility as a direct consequence of functional suppression of their well-established innate immune capacity due to a rapid re-exposure event or, even much worse and long-lived, due to vaccination.

The likelihood of rapid re-exposure to Sars-CoV-2 after previous infection dramatically increases when highly infectious variants expand in prevalence. Such an expansion in prevalence directly results from mass vaccination campaigns as mass vaccination turns vaccinees into an excellent breeding ground for naturally selected S-directed immune escape variants.”

10/05/21.  Pro-vax John Campell, Ph.D. says COVID Vaccines Are Being Administered Incorrectly, Expert Tells Jimmy Dore  Incorrect injection techniques being recommended by the CDC, WHO and vaccine manufacturers are increasing post-vaccine blood clotting and damages to the brain, lungs, and heart.  Other videos: Inadvertant intravenous injections and  Aspiration, more information        See these two papers:

Dr. Richard Fleming, MD, PhD, JD, who has studied spike proteins in his research since the 1990’s and explains beginning at the 2:14:30 mark how the harm is done and will continue to worsen.   October 2, 2021.  The first part of Dr. Fleming’s talk begins at roughly the 1:25:30 mark and explains how these mRNA gene technologies work, as well as the misleading statistics that were used in the media propaganda to promote the gene technology injections to the public, fooling even medical doctors who are too busy to delve into the details of the statistical analyses.

My Jaw DROPPED when I Tested Someone’s Immune System After the 2nd mRNA Jab.  By Dr. Nathan Thompson What does the mRNA COVID vaccine do to the human immune system? Sep 28, 2021.

Vaccine Immune Interations and the Booster Shots By Doctors for COVID Ethics. How and why Covid-19 vaccines incite immunological attack on blood vessel walls.  By now, most people know COVID-19 vaccines can cause blood clotting and bleeding. Some readers may be aware that reports of death following COVID-19 vaccination outnumber those for all vaccines combined since records began, in 1990, in the official US database VAERS. Eminent independent scientists and researchers in the fields of immunology and microbiology have been writing to medical regulators since early 2021 [3], warning of vaccine-related blood clotting and bleeding, including that the official data on blood abnormalities post-vaccination likely represent “just the tip of a huge iceberg”

A Report on Myocarditis Adverse Events in the U.S. Vaccine Adverse Events Reporting System (VAERS) in Association with COVID-19 Injectable Biological Products JessicaRose PhD, MSc, BSc1. Peter A.McCulloughMD, MPH1 October 1, 2021. https://doi.org/10.1016/j.cpcardiol.2021.101011 Myocarditis rates reported in VAERS were significantly higher in youths between the ages of 13 to 23 (p<0.0001) with ∼80% occurring in males. Within 8 weeks of the public offering of COVID-19 products to the 12-15-year-old age group, we found 19 times the expected number of myocarditis cases in the vaccination volunteers over background myocarditis rates for this age group. …

These findings suggest a markedly higher risk for myocarditis subsequent to COVID-19 injectable product use than for other known vaccines, and this is well above known background rates for myocarditis. COVID-19 injectable products are novel and have a genetic, pathogenic mechanism of action causing uncontrolled expression of SARS-CoV-2 spike protein within human cells. [KD: Math Note: Normal background rate of myocarditis in children for one year is 1 in 100,000. However, in vaccinated children aged 12 to 15 in just 8 weeks out of 3,430,741 children vaccinated there were  97 reported cases to the CDC’s VAERS.

However, normally expected number in the same time period would be 8/52 * 34.3 = ~5 myocarditis cases. Thus, the rate of myocarditis due to the vaccine is at bare minimum 19 times higher than the normal background rate. Given VAERS is known to be under-reported by a factor of 5 to 50+, and the lack of post-vax testing, the more likely number of myocarditis cases in 12 to 15 year olds due to COVID mRNA/DNA vaccines as of June 30th is more likely to be 95+ times normal or more than 485 children in just 8 weeks.  The COVID vaccine is killing many Children.]

Continued on next page…

Pages: 1 2 3 4 5 6 7 8 9 10