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Conspiracy Theorists Were Right; It Is a Killer Jab! It All Makes Sense Once You Realize They Want to Kill Us All!

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The Conspiracy Theorists Were Right; It IS a “Poison-Death Shot”

“I’ll do one more mind experiment with you: If everyone on the planet were to get Covid and not get treated, the death-rate globally would be less than half a percent. I’m not advocating for that, because 35 million people would die. However, if we follow the advice of some of the global leaders– like Bill Gates who said last year said “7 billion people need to be vaccinated”– then the death-rate will be over 2 billion people! SO, WAKE UP! THIS IS WORLD WAR 3! We are seeing a level of malevolence that we haven’t seen in the history of humanity!” Dr. Vladimir Zelenko, Author of The Zelenko “Early Treatment” Protocol that saved thousands of Covid-19 patients. (“Zelenko schools the Rabbinic Court”, Rumble; start at 11:45 minutes)

Did the regulators at the FDA know that all previous coronavirus vaccines had failed in animal trials and that the vaccinated animals became either severely ill or died?  Yes, they did.

Did they know that previous coronavirus vaccines had a tendency to “enhance the infection” and “make the disease worse”?  Yes.

Did Dr Anthony Fauci know that coronavirus vaccines had repeatedly failed and increased the severity of the infection?  Yes, he did. (See here: Fauci on ADE)

Did the drug companies conduct any animal trials prior to the FDA’s approval that would have convinced a reasonable person that the vaccines were safe to use on humans?  No, they didn’t.
Did they complete long-term clinical trials to establish whether the vaccines were safe?  No, there were no long-term clinical trials.
Did they conduct any biodistribution studies that showed where the substance in the injection goes in the body?  They did, but the data was not made available to the public.
Do the contents of the vaccine largely collect in various organs and in the lining of the vascular system?  Yes, they do.
Do large amounts of the substance accumulate in the ovaries?  Yes.
Will this effect female fertility and a woman’s ability to safely bring a baby to term?

The drug companies are currently researching this. The results are unknown.
Does the vaccine enter the bloodstream and collect in the lining of the blood vessels forcing the cells to produce the spike protein?  Yes.
Is the spike protein a “biologically active” pathogen?  Yes, It is.
Does the spike protein cause blood clots and leaky blood vessels in a large percentage of the people that are vaccinated?  It does, although the blood clots are mostly microscopic and appear in the capillaries. Only a small percentage of vaccinees get strokes or suffer cardiac arrest.
Should people be made aware of these possible bad outcomes before they agree to get vaccinated? (“Informed consent”)  -  Yes.

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Did the FDA know that Pfizer had “identified vaccine-associated enhanced disease, including vaccine-associated enhanced respiratory disease, as an important potential risk”?  Yes, they did, but they did not demand that Pfizer fix the problem. Here’s more:

“The FDA noted that Pfizer, “identified vaccine-associated enhanced disease, including vaccine-associated enhanced respiratory disease, as an important potential risk”. The EMA similarly acknowledged that “vaccine associated enhanced respiratory disease” was “an important potential risk… that may be specific to vaccination for COVID- 19”.

Why neither regulator sought to exclude such dangers prior to emergency use authorization is an open
question that all doctors and patients are entitled to ask. Why medical regulators failed to investigate the
finding that large vaccine particles cross blood vessel walls, entering the bloodstream and posing risks of blood clotting and leaky vessels is yet another open question again.” (“Open Letter to the EMA and European Parliament”, Doctors for Covid Ethics)

Did the drug companies vaccinate the people in the placebo group after the clinical trials in order to conceal the difference in the long-term health outcomes between the two groups?  That is the conclusion a rational person would make.

So, they nuked the trials?  Yes.

Did the FDA largely shrug-off its regulatory duties and abandon its normal standards and protocols because

a– It wanted to rush the Covid vaccines into service as rapidly as possible?
b– It knew the Covid-19 vaccine would never meet long-term safety standards?

We don’t know yet, but the adverse events report strongly suggests that the Covid-19 vaccine is hands-down the most dangerous vaccine in history.

Is the FDA rushing the “boosters” without proper testing?  Yes, it is. Here’s a clip from author Alex Berenson’s latest at Substack:

“Pfizer basically hasn’t bothered to test the booster AT ALL in the people actually at risk – it conducted a single “Phase 1” trial that covered 12 people over 65. The main Phase 2/3 booster trial (beware efforts to cover multiple “phases” of drug research at once, you want it bad you get it bad) included no one over 55.

No one.

As in NONE.” (“Are you kidding me, Pfizer, volume 1 gazillion”, Alex Berenson, Substack)

Have the boosters been modified or improved to meet the changes in Delta variant?  No.

Is there any additional risk in taking a booster-shot after already taking two experimental gene-based vaccines in less than a year?  Considerable risk. Here’s more from the Doctors for Covid Ethics:

“Given that booster shots repeatedly boost the immune response to the spike protein, they will progressively boost self-to-self immune attack, including boosting complement-mediated damage to vessel walls.

Clinically speaking, the greater the vessel leakage and clotting that subsequently occurs, the more likely that organs supplied by the affected blood flow will sustain damage. From stroke to heart attack to brain vein thrombosis, the symptoms can range from death to headaches, nausea and vomiting, all of which heavily populate adverse reactions to COVID-19 vaccines.

As well as damage from leakage and clotting alone, it is additionally possible that the vaccine itself may leak into surrounding organs and tissues. Should this take place, the cells of those organs will themselves begin to produce spike protein, and will come under attack in the same way as the vessel walls. Damage to major organs such as the lungs, ovaries, placenta and heart can be expected ensue, with increasing severity and frequency as booster shots are rolled out.” (“Open Letter to the EMA and European Parliament“, Doctors for Covid Ethics)

So, it’s the double-whammy. On the one hand, the booster will perform largely like the original vaccine, penetrating cells and forcing them to produce spike protein which, in turn, generates blood clots and leaky blood vessels. And, on the other, the newly-produced S proteins trigger a damaging immune response in which the complement system attacks and destroys the cells that line the inside of the blood vessels. Every additional booster will intensify this process weakening the vascular system and increasing the clotting. If the Doctors are correct in their analysis, then we could see a sharp uptick in all-cause mortality in the heavily-vaccinated countries in less than a year. Cardiac arrests are already rising.

Here’s another question that’s worth mulling over: Was there any reason for the regulators at the FDA to think that these problems would not arise following the launching of the vaccine campaign?

No. They should have known there would be problems as soon as they saw that the vaccine did not stay in the shoulder as it was supposed to. The vaccine wasn’t supposed to enter the bloodstream and spread across the body leaving billions of spike proteins in its wake. (The spike protein is a cytotoxin, a cell killer. It is not an appropriate antigen for stimulating an immune response. It is a potentially-lethal pathogen that poses a threat to one’s health even if it is separated from the virus.) Nor was the vaccine supposed to trigger Antibody-Dependent Enhancement (ADE) which is the condition we hinted at above when referring to “vaccine-associated enhanced disease”. Here’s a brief explanation:

“ADE has proven to be a serious challenge with coronavirus vaccines, and this is the primary reason many have failed in early in-vitro or animal trials. For example, rhesus macaques who were vaccinated with the Spike protein of the SARS-CoV virus demonstrated severe acute lung injury when challenged with SARS-CoV, while monkeys who were not vaccinated did not. Similarly, mice who were immunized with one of four different SARS-CoV vaccines showed histopathological changes in the lungs with eosinophil infiltration after being challenged with SARS-CoV virus. This did not occur in the controls that had not been vaccinated. A similar problem occurred in the development of a vaccine for FIPV, which is a feline coronavirus.” (“Is the Coronavirus Vaccine a Ticking-Time Bomb?”, Science with Dr. Doug)

Is this what we are seeing right now? In all the countries that launched mass-vaccination campaigns early (Israel, Iceland, Scotland, Gibraltar and UK) cases, hospitalizations and deaths are rising faster in the vaccinated portion of the population than the unvaccinated. Why?

Are they really experiencing a fourth or fifth wave or have the vaccines generated “inactivity-enhancing” antibodies that make the disease worse? This 2-minute video helps to clarify what’s going on:

Vaccines are made to a specific variant. And when that variant mutates, the vaccine no longer recognizes it. It’s like you are seeing a completely new virus. And, because that is so, you actually get more severe symptoms when you are vaccinated against one variant and it mutates and then your body sees the other variant. The science shows, that if you get vaccinated in multiple years (for the flu), you are more likely to get severe disease, you are more likely to get viral replication, and you are more likely to be hospitalized…. We are seeing the same thing in Covid with the Delta variant. So we are actually mandating that people get a vaccine when they can actually get more sick when they are exposed to the virus...In fact, this week, a paper came out that showed that–with the Delta variant– when you are vaccinated your body is supposed to make antibodies that neutralize the virus, but they were supposed to neutralize the old variant. When they see this new variant, the antibodies take the virus and help it infect the cells.” (“Expert testimony on mandatory vaccinations”, Dr Christina Parks PhD., Rumble, start at minute 5:05)

Repeat: “If you get vaccinated in multiple years, you are more likely to get severe disease, you are more likely to get viral replication, and you are more likely to be hospitalized…. With the Delta variant– when you are vaccinated …. the antibodies take the virus and help it infect the cells.”

This is ADE, and this is probably why hospitalizations and deaths are rising among the vaccinated in Israel, UK and the rest. True, the Delta variant is less lethal than the Wuhan virus but, unfortunately, that rule does not apply to those who have been vaccinated and whose antibodies promote the uptake of the virus into their cells. This increases the viral replication function that increases the severity of the disease. In short, people are getting sicker because they were vaccinated. Here’s another short video that helps to explain:

It’s not the variant that intensifies the disease, it’s the fact that the vaccine targets one narrow endpoint, the spike protein, that gradually adapts to survive. As the virus progressively learns to avoid the vaccine, vaccine-induced immunity wanes. Natural immunity produces broad, robust immunity to the whole virus not merely one part of it. It is strong and enduring.

So how will the vaccinated fight new forms of the virus, after all, the vaccine is not a medicine that overpowers a particular pathogen. It is a subtle (genetic) reprogramming of the immune system that forces one’s cells to produce a particular version of the spike protein. Boosters that stimulate production of the same protein will have only modest impact. In short, boosters are still fighting the last war.

Also, as we mentioned above, coronavirus vaccines tend to create antibodies that “enhance infectivity” when they encounter adapted forms of the virus. That means that millions of inoculated people will now face forms of the virus for which they have almost no protection and for which their compromised immune systems can only provide limited help. Here’s more from the article above:

“Right now, the fatality rate of the virus is estimated to be approximately 0.26%, and this number seems to be dropping as the virus is naturally attenuating itself through the population. It would be a great shame to vaccinate the entire population against a virus with this low of a fatality rate, especially considering the considerable risk presented by ADE. I believe t his risk of developing ADE in a vaccinated individual will be much greater than 0.26%, and, therefore, the vaccine stands to make the problem worse, not better. It would be the biggest blunder of the century to see the fatality rate of this virus increase in the years to come because of our sloppy, haphazard, rushed efforts to develop a vaccine with such a low threshold of safety testing and the prospect of ADE lurking in the shadows.” (“Is the Coronavirus Vaccine a Ticking-Time Bomb?”, Science with Dr. Doug)

“Blunder”, he says?  It wasn’t a blunder. It was deliberate. The Covid-19 vaccine was supposed to fail like all the coronavirus vaccines before it. That’s the point. That’s why the drug companies skipped the animal testing and long-term safety trials. That’s why the FDA rushed it through the regulatory process and suppressed the other life-saving medications, and silenced all critics of the policy, and pushed for universal vaccination regardless of the risks of blood clotting, cardiac arrest, stroke and death. And that’s why the world is on the threshold of an “international catastrophe of mass mortality.” It’s because that’s how the strategy was planned from the very beginning.

The vaccine isn’t supposed to work, it’s supposed to make things worse. And it has! It’s increased the susceptibility of millions of people to severe illness and death. That’s what it’s done. It’s a stealth weapon in an entirely new kind of war; a war aimed at restructuring the global order and establishing absolute social control. Those are the real objectives. It has nothing to do pandemics or viral contagion. It’s about power and politics. That’s all.

It All Makes Sense – Once You Realize They Want to Kill Us All!

“For we wrestle not against flesh and blood, but against the rulers of the darkness of this world, against spiritual wickedness in high places.” Ephesians 6:12

 

 

“It is now apparent that these products in the blood stream are toxic to humans. An immediate halt to the vaccination programme is required while an independent safety analysis is undertaken to investigate the full extent of the harms, which the UK Yellow Card data suggest includes thromboembolism, multi-system inflammatory disease, immune suppression, autoimmunity and anaphylaxis, as well as Antibody Dependent Enhancement (ADE).” Tess Lawrie, Evidence-Based Medicine Consultancy

Question– Have the mRNA vaccines been tested on animals?

Answer– Yes, they have.

Question– Were the animal trials successful?

Answer– Yes and no.

Yes, the experiments on mice showed that a low dose of the vaccine induces a robust antibody response to the infection.

But, no, the antibodies were not able to attack the spike protein from a different strain of the virus.

Question– I’m not sure what that means? Do you mean that the vaccine DOES provide some limited protection from the original (Wuhan) virus, but does not necessarily provide protection from the variants?

Answer– That’s right, but it’s a bit more complicated than that because– as the virus changes — the antibodies that helped to fight the original virus can actually enhance the “infectivity” of the variant. In other words, vaccine-generated antibodies can switch-sides and increase the severity of the illness. Simply put, they can make you sicker or kill you. Scientists have known this for a long time. Check out this clip from a 2005 research paper:

“A jab against one strain might worsen infection with others….

In the.. study, Gary Nabel of the National Institute of Allergy and Infectious Diseases.. injected mice with spike protein from a SARS virus taken from a human patient infected in early 2003. They then collected the antibodies the animals produced.

In lab experiments, they showed that these antibodies were unable to attack spike protein from a different strain of SARS, isolated from a patient infected in late 2003….The team next tested whether the antibodies would attack spike proteins from two SARS strains isolated from civets, from which the virus is thought to have originally jumped into humans. In this case, they found hints that the antibodies actually boosted the ability of the virus to infect cells.

The results show that the virus changes over time, so that a strain that crops up in one outbreak might be quite different from that in a later outbreak. “This virus is not standing still and we need to take this into account,” Nabel says.

This raises the prospect that a vaccine against one strain of SARS virus could prove ineffective against others. Worse, a jab against one strain might even aggravate an infection with SARS virus from civets or another species. “It’s obviously a concern,” Nabel says..
This would not be the first case where exposure to one strain of a virus can worsen infection with another.” (“Caution raised over SARS vaccine”, Nature)

Question– I’m still confused. Can you summarize what they’re saying?

Answer– Sure. They’re saying that scientists have known for nearly two decades that vaccines narrowly aimed at just one protein are bound to fail. They’re saying that the spike protein is highly-adaptable and capable of changing its shape to survive. They’re saying that vaccines aimed at the spike protein will inevitably produce variants that evade vaccine-generated antibodies. They’re saying that by narrowing the vaccine’s focus to the spike protein alone, the drug companies have ensured that previously helpful antibodies will do an about-face, allow the virus to enter healthy cells, replicate at will, and cause sickness or death. They are saying that the current crop of vaccines is in fact perpetuating the pandemic. And–since the science has been clear for the last 16 years– we can add one more observation to the list, that is, that the current approach to mass vaccination is neither haphazard, slapdash or random. It is intentional. The vaccination campaign managers are deliberately ignoring the science in order to sustain a permanent state of crisis. Science is being manipulated to achieve a political objective.

Question– I think you’re exaggerating, but I’d like to get back to the animal trials instead of arguing politics. As you probably know, the reports in the media do not square with your analysis, in fact, all of the articles in the MSM say the animal trials were a rousing success. Here’s a short blurb that I found today that confirms what I’ve been saying:

“…vaccination of nonhuman primates with the mRNA vaccine induced robust SARS-CoV-2 neutralizing activity and notably, rapid protection in the upper and lower airways….” (Covid-19, NIH.gov)

Question– Are you suggesting the authors are lying?

Answer– No, they are not lying. They’re just not telling you the whole truth, and you need to know the whole truth so you can make an informed decision. The vaccines DO provide some (temporary) protection. We don’t dispute that. They also trigger a strong immune response. We don’t dispute that either. But what difference does it make? Let me explain: Let’s say, you have a really bad head cold so you take a new medication that you think will relieve the pain. And–sure enough– an hour after taking the pills– Presto — your congestion and headache are completely gone. That’s fantastic, right? Wrong, because what you fail to realize is that the medication is laced with slow-acting strychnine that kills you three days later. Do you still think it was a good idea to take the medication?

Of course, not. And the same rule applies to these vaccines which do, in fact, boost your antibodies and provide some fleeting “immunity”. But they can also kill you. Don’t you think that should be factored in to your decision? Keep in mind, people have died 3, 4, 5 weeks after inoculation without any prior warning. Many of them might have even been bursting with antibodies, but they’re still dead. Can you see the problem?

Question– Okay, but there’s still this matter about the animal trials. The media says that the drug companies performed the animal trials and they were successful. Do you disagree with that?

Answer– They were not successful and the “fact checkers” that were hired to discredit vaccine critics like me, have deliberately mischaracterized what happened in the trials. For example, here’s a typical “fact checker” article titled “COVID-19 vaccines did not skip animal trials because of animal deaths” by Reuters. Here’s an excerpt:

“Posts claiming that COVID-19 vaccine producers skipped animal trials due to the animals in those trials dying are false. Pfizer-BioNTech, Moderna and Johnson & Johnson, which have been granted emergency authorization use by the Food and Drug Administration (FDA) in the United States, all conducted animal trials and had no significant safety concerns to report.”

Sounds reassuring, right? But then they say:

“Due to time constraints and the urgency to find a vaccine for COVID-19, Moderna and Pfizer did receive approval to run animal testing and early trials on humans at the same time, as opposed to fully completing animal trials before moving on to human trials. This, however, does not mean animal trials were skipped or that the safety of the vaccines were compromised.”

Let me see if I got this straight: The drug companies were in such a hurry that they conducted their minimalist animal trials at the same time as their human trials (which is unprecedented) and then rushed the results to the FDA so they could be rubber stamped and waved through under the Emergency Use Authority?

Is that how it went down?  Yes, it is.

But if they were rushed through in a couple months, then the “fact checkers” are tacitly admitting that there is no long-term safety data. And there IS no long-term safety data, nor is there any attempt to disprove the research from the earlier trials where the ferrets, mice and other animals died following injection of mRNA vaccines. They don’t deny it, they just ignore it as if sweeping it under the rug will make it all go away. Here’s a clip from the research paper that Reuters refers to in its article:

“We demonstrate that the candidate vaccines… respectively—induce strong antigen-specific immune responses in mice and macaques….Both (vaccines) protected 2–4-year-old macaques from challenge with infectious SARS-CoV-2, and there was reduced detection of viral RNA in immunized macaques as compared to those that received saline.” (Note–We’ve already acknowledged that the vaccines do produce a strong immune response. Here’s more:)

“Neutralizing GMTs declined by day 56 (35 days after dose 2), consistent with the contraction phase; however, they remained well above the GMT of the human sera panel. The duration of the study was not long enough to assess the rate of decline during the plateau phase of the antibody response.” (“BNT162b vaccines protect rhesus macaques from SARS-CoV-2”, Nature)

Can you see what’s going on? The trial was only 56 days-long, in fact, none of the animal trials exceeded 56 days. Think about that for a minute. The reason the animals died in prior trials is because they were exposed to a mutated version of the (wild) virus that eventually killed them. That’s how ADE (antibody-dependent enhancement) works. It doesn’t happen overnight and it doesn’t happen in 56 days. It takes much longer than that for a mutated version of the virus to emerge and reinfect the host. The drug companies know that. They’re not stupid. So the fact that the animals mounted a strong immune response is completely irrelevant. We KNOW they mounted a strong immune response. We also know they died some months later when a different strain of the virus emerged. Bottom line: The production of antibodies does not mean a drug is safe.

The obvious purpose of the trials was to get the vaccines over the finish-line before anyone figured out what was going on. It’s the same reason why the drug companies “unblinded” their human trials after the vaccines got the green light from the FDA. Shortly after the trials were concluded, the people in the placebo arm were allowed to get vaccinated.

Why would they do that? Why would they vaccinate the people who willingly allowed themselves to be guinea pigs for the sake of public health, only to vaccinate them shortly after, thus, eliminating any chance of finding out what the long-term safety issues might be? It makes no sense, does it?

Take a look at this short clip from the British Medical Journal whose scientists are equally bewildered:

“The (drug) companies say they have an ethical obligation to unblind volunteers so they can receive the vaccine. But some experts are concerned about a “disastrous” loss of critical information if volunteers on a trial’s placebo arm are unblinded

Although the FDA has granted the vaccines emergency use authorization, to get full license approval two years of follow-up data are needed. The data are now likely to be scanty and less reliable given that the trials are effectively being unblinded.

Consumer representative Sheldon Toubman, a lawyer and FDA advisory panel member, said that Pfizer and BioNTech had not proved that their vaccine prevents severe covid-19. “The FDA says all we can do is suggest protection from severe covid disease; we need to know that it does that,” he said.

He countered claims, based on experience with other vaccines, six weeks of follow-up was long enough to detect safety signals. Six weeks may not be long enough for this entirely new type of “untested” [mRNA] vaccine, Toubman said.

Goodman wants all companies to be held to the same standard and says they should not be allowed to make up their own rules about unblinding. He told The BMJ that, while he was “very optimistic” about the vaccines, “blowing up the trials” by allowing unblinding “will set a de facto standard for all vaccine trials to come.” And that, he said, “is dangerous.”

(“Covid-19: Should vaccine trials be unblinded?” The British Medical Journal)

Do you like his choice of words: “blowing up the trials”? Do you think it is a fair description of what the drug companies did?  Yes, it is.

And what possible motive would the drug companies have to blow up the trials? I can see only two possibilities:

  1. They think their vaccine is so terrific, it will save the lives of many of the people in the placebo group.
  2. They expect a high percentage of the people in the vaccine group to get either severely sick or die, so they want to hide the evidence of vaccine-linked injury.

Which is it?

You know the answer. Everyone watching this farce knows the answer.

Question– Okay, so let’s cut to the chase: Are the vaccines are safe or not?

No, they are not safe. The way we decide whether a drug is safe or not is by putting it through a rigorous process of testing and clinical trials. After the testing, the data is passed on to physicians, statisticians, chemists, pharmacologists, and other scientists who review the data and make their recommendations or criticisms. That didn’t happen with the Covid vaccines, in fact, all the normal standards and protocols were suspended in the name of “urgency”. But many believe that the “urgency” was manufactured to push through vaccines that would never have been approved on their own merits. All you have to do is look through the vaccine injury data (VAERS) and you’ll see this is the most lethal medical intervention of all time and, yet, the public health experts, the media and the government keep crowing that they’re “safe and effective”. It’s nonsense and the drug companies know it’s nonsense which is why they reject all liability for the people that are going to be killed by these “poison-death shots.”

Do you know what goes on inside your body after you are injected with one of these “gene based” vaccines?

Once the vaccine enters the bloodstream it penetrates the cells that line the blood vessels forcing them to produce spike proteins that protrude into the bloodstream like millions of microscopic thorns. These thorns activate blood platelets which trigger blood clotting followed shortly after by an immune response that destroys the infected cells thus weakening the vascular system while draining the supply of killer lymphocytes. In this way, the vaccine launches a dual attack on the body’s critical infrastructure causing widespread tissue damage throughout the circulatory system while leaving the immune system less able to fend off future infection.

Now if you think you can have a long-and-happy without a functioning circulatory system, then none of this matters. But if you’re bright enough to realize that wreaking havoc on your vascular system is the fast-track to the graveyard, then you’ll probably understand that injecting these “poison-death shots” is a particularly bad idea.

By the way, it’s a real stretch to call these hybrid injections, “vaccines”. They have about as much in common with a traditional vaccine as a python does with a coffee table. Nothing. The “vaccine” moniker was chosen in order to shore-up public confidence, that’s all. It’s part of a marketing strategy. There is no real similarity. The majority of people trust vaccines and see them as a shining example of medical achievement. The drug companies wanted to tap into that trust and use it for their own purposes. That’s why they called it a “vaccine” instead of “gene therapy” which more accurately describes ‘what it does.’ But–like we said– it’s just a marketing strategy.

Have you ever wondered how the drug companies were able to roll out their own-individual vaccines just weeks apart from each other? That’s a pretty good trick, don’t you think; especially since vaccine development typically takes from 10 to 15 years. How do you think they managed that? Here’s an excerpt from an article which provides a little background on the topic:

“The virus behind the outbreak that began in Wuhan, China, was identified on Jan. 7. Less than a week later — on Jan. 13 — researchers at Moderna and the NIH had a proposed sequence for an mRNA vaccine against it, and, as the company wrote in government documents, “we mobilized toward clinical manufacture.” By Feb. 24, the team was shipping vials from a plant in Norwood, Mass., to the National Institute of Allergy and Infectious Diseases, in Bethesda, Md., for a planned clinical trial to test its safety.” (“Researchers rush to test coronavirus vaccine in people without knowing how well it works in animals”, Stat)

Got that? “The virus broke out in Wuhan…on Jan. 7, and less than a week later Moderna had a proposed sequence for an mRNA vaccine against it???

Really? Is that the same Moderna that had been playing-around with mRNA for over a decade but was never able to successfully bring a vaccine to market?

Yep, the very same company. Here’s more:

“And by Feb. 24, the team was shipping vials from a plant in Norwood, Mass??”

Wow! Another Covid miracle! You almost get whiplash watching these companies crank out their “wonder drugs” at record-breaking speed.

Keep in mind, there’s a very high probability that the virus was man-made, (In other words, it’s a bioweapon.) and the people who have been implicated in the funding and creation of that bioweapon are also closely aligned with the big drug companies that have produced the antidote in record time that has already netted tens of billions of dollars in profits for a drug for which there was no reliable animal testing, no long-term safety data, and no formal regulatory approval.

So I’ll ask you again: Doesn’t that all sound a bit suspicious?

Is it really that hard to see the outline of a political agenda here? After all, aren’t the drug companies working with the regulatory agencies that are working with the public health officials that are working with the media that are working with the corrupted politicians that are working with the Intel agencies that are working with the meddling globalist billionaires that are working with the giant private equity firms that oversee the entire operation pulling the appropriate strings whenever needed?

It sure looks like it.

And, don’t the tectonic social changes we’ve seen in the last year have more to do with a broader scorched-earth campaign launched by the “parasite class” against the rest of humanity than they do with a fairly-mild virus that kills mainly old and frail people with multiple underlying health conditions?

Right, again. In fact, many have noticed the cracks in the pandemic artifice from the very beginning, just as many have pointed out that the virus-meme is just the mask behind which parasites continue to conduct their global restructuring project. In short, it’s all about politics; bare-knuckle, take-no-prisoners NWO politics.

Answer– You’ve asked a number of questions about the animal trials, but none about the biodistribution and the pharmacokinetics studies that were done at the same time. Why is that? (Note--Pharmacokinetics; “the branch of pharmacology concerned with the movement of drugs within the body.”)

Question– I didn’t know there were any. Did the media report on them?

Answer– No, they didn’t. They completely ignored them, even though they were produced by Pfizer and provide essential information about where the substance in the vaccine goes in the body, in what amounts, and for how long. By knowing how the drug is distributed, it is possible to make educated assumptions about its effect on the organs and other tissue. In other words, these studies are invaluable. The Doctors for Covid Ethics have done extensive research on the studies and written a report titled “The Pfizer mRNA vaccine: pharmacokinetics and toxicity”. Here’s a few excerpts that help to illustrate the dangers of the vaccines:

“As with any drug, a key consideration for the toxicity of the COVID mRNA vaccines is where exactly in the body they end up, and for how long they will stay there. Such questions, which are the subject of pharmacokinetics, are usually thoroughly investigated during drug development. Initial studies on pharmacokinetics and also on toxicity are carried out in animals… this document has rather far-reaching implications: it shows that Pfizer—as well as the authorities that were apprised of these data— must have recognized the grave risks of adverse events after vaccination even before the onset of clinical trials. Nevertheless, Pfizer’s own clinical trials failed to monitor any of the clinical risks that were clearly evident from these data, and the regulatory authorities failed to enforce proper standards of oversight. This dual failure has caused the most grievous harm to the public….

What do Pfizer’s animal data presage for biological effects in humans?

  • Rapid appearance of spike protein in the circulation.
  • Toxicity to organs with expected high rates of uptake, in particular placenta and
    lactating breast glands
  • Penetration of some organs might be higher with the real vaccine than with this
    luciferase model…The rapid entry of the model vaccine into the circulation means that we must expect the spike protein to be expressed within the circulation, particularly by endothelial cells. ( Endothelial- The thin layer of cells lining the blood vessels) We have seen before that this will lead to activation of blood clotting through direct activation of platelets and also, probably more importantly, through immune attack on the endothelial cells….

Summary

Pfizer’s animal data clearly presaged the following risks and dangers:

  • blood clotting shortly after vaccination, potentially leading to heart attacks, stroke, and venous thrombosis
  • grave harm to female fertility
  • grave harm to breastfed infants
  • cumulative toxicity after multiple injections

With the exception of female fertility, which can simply not be evaluated within the short period of time for which the vaccines have been in use, all of the above risks have been substantiated since the vaccines have been rolled out—all are manifest in the reports to the various adverse event registries. Those registries also contain a very considerable number of reports on abortions and stillbirths shortly after vaccination, which should have prompted urgent investigation.
….
Of particularly grave concern is the very slow elimination of the toxic cationic lipids. In persons repeatedly injected with mRNA vaccines containing these lipids… this would result in cumulative toxicity. There is a real possibility that cationic lipids will accumulate in the ovaries. The implied grave risk to female fertility demands the most urgent attention of the public and of the health authorities.

Since the so-called clinical trials were carried out with such negligence, the real trials are occurring only now—on a massive scale, and with devastating results. … Calling off this failed experiment is long overdue. Continuing or even mandating the use of this poisonous vaccine, and the apparently imminent issuance of full approval for it are crimes against humanity.” (“The Pfizer mRNA vaccine: pharmacokinetics and toxicity”, The Doctors for Covid Ethics)

Don’t you think people are entitled to know what the government wants to inject into their bodies? Don’t you think they have a right to know how it will effect their immune systems, their vital organs and their overall health? Don’t you think they have the right to decide for themselves which drugs they will take and which they will refuse to take?

Forcing someone to take a drug he does not want, is not just wrong. It’s unAmerican. Which is why people should reject vaccine mandates as a matter of principle. They are an attack on personal liberty, the foundation of our constitutional system. It’s a principle worth dying for.

As for the mass vaccination campaign, it is the most maniacally-genocidal project ever concocted by man. There’s simply no way to calculate the amount of suffering and death we are about to face for trusting people whose policies were obviously shaped by their undiluted hatred of humanity. As German microbiologist Dr. Sucharit Bhakdi said:

“In the end, we’re going to see mass illness and deaths among people who normally would have had wonderful lives ahead of them.”

It is a great tragedy, indeed!

 

Article by Mike Whitey



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    • Theosophist

      Very Good Article! But way more nefarious, as in the worst part of the vax actually created by Alien technology not of this world. For purpose of turning humans into hapless cyborgs, programable serfs so they can steal the wealth of the entire planet forever more.

      Article from James Rink sight (web address at end). James is another hero of humanity!

      What’s in there is so horrible that the samples ended up inside a high security Bio-Hazard container. They were subsequently disintegrated with high energy. What is in there we can’t even share with you, because I have no way to explain it as it would need to be explained. For example, if Dr. Alex wants data on what happens and the bio-chemical processes caused by the vaccines, I simply cannot give it to him.

      I see this as extremely serious because people will not understand what is there, they will see it as fantasy or inventions. The same doctors against plandemic will not make sense of nano bots, because their labs are unable to detect or understand the functioning of nano graphite, at the atomic or molecular level.

      Gosia: Why is there no way to explain it?

      Anéeka: Because the technology present there in the samples from the 3 factories exceeds human understanding, so what I say sounds crazy science fiction and over exaggerated. Perhaps even hurting credibility. I don’t even have the medical vocabulary to describe it, because there is none. It can be described on a… layman’s level but it will NOT…

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