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For all the brainless Commie Vaxtardz out there:
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https://www.theblaze.com/op-ed/horo...d-released-by-judge-shows-shocking-risk-level
Horowitz: Pfizer vaccine injury data ordered released by judge shows shocking risk level
Any time one even mentions a story, data, or even VAERS numbers showing serious injury or death resulting from the vaccine, the bio-medical state lobby close their ears and shout while their censors in Big Tech label it as misinformation. But now we have it from the horse’s mouth – Pfizer’s own vaccine injury data – a shocking amount of death and injury that is likely under-reported. This means that the FDA knew from day one these vaccines were unsafe to the point that they would typically be denied authorization, and certainly not funded, mandated, and marketed with a budget and energy that have never been placed behind a product since the dawn of time.
Pursuant to an agreement based on a FOIA lawsuit, the FDA has agreed to release 500 pages of vaccine data documents per month. There is a total of 329,000 pages of documents containing the information the agency relied upon to approve the shots, but they have asked a court to give them 55 years to release them. Last week, the FDA released the first five documents to a group of scientists suing for the information, and one of them reveals Pfizer’s data on adverse events through Feb. 28. The 38-page document details the cumulative post-authorization safety data reported to Pfizer’s system during the early days of the mass vaccination campaign.
In total, Pfizer discloses the existence of 42,086 adverse event case reports containing 158,893 total events, including 1,227 deaths. 25,957 of the events were classified as “Nervous system disorders.” So for those who think that somehow VAERS is not accurate or is overreporting deaths, these are numbers straight from the horse’s mouth just through February. Remember, it is extremely hard to trace many serious events back to the vaccine, including death, especially if there is a few weeks’ lag time, and most especially with people already in advanced age. So these are just the ones that were “submitted voluntarily, and the magnitude of underreporting is unknown.”
Full stop right there. Under any other circumstance, such a vaccine would have been removed from the market right away, certainly not fully endorsed, marketed, funded, and mandated by government. It was so bad that Pfizer reveals, “Due to the large numbers of spontaneous adverse event reports received for the product, the MAH has prioritized the processing of serious cases” and also had to hire more full-time employees to handle the reporting. How was it ethical for the FDA to withhold this information from the public, and how can it ever be ethical to mandate such a shot, even if one believes that, in general, a government could wield such authority? This is especially true now that we know its efficacy is minimal at best and downright enhances the virus at worst.
Imagine if there were a third-party audit of vaccine adverse events by someone other than the manufacturer. Let’s not forget that according to the lawyer for the de Garay family, whose 12-year-old daughter suffered a debilitating injury from the shot during the actual clinical trial, Pfizer and the feds tried to do everything possible to deny that the vaccine caused the injury. This is for someone in the supposedly carefully monitored trial and this is for a 12-year-old. You can imagine how many seniors got the shots and were injured or died, yet the families never reported it because they chalked it up to end-of-life health decline or morbidity.
The time has come for Republican governors to stop denying the problems with these shots and pick up the slack of regulatory oversight where the feds have engaged in criminal negligence. It is impossible to deny the safety signals and refrain from taking investigative and regulatory actions to provide state residents with informed consent. The safety signals for blood disorders and cardiac issues alone are enormous. Consider the fact that researchers from the University of Hong Kong bluntly concluded, “There is a significant increase in the risk of acute myocarditis/pericarditis following Comirnaty vaccination among Chinese male adolescents, especially after the second dose.” Now remember that this is the only shot even approved for teenagers, while Moderna, which has a stronger dose, is banned in many European and Asian countries for those under 30.
At some point the concerning safety signals have to matter. One of the most troubling signals is the inordinate number of professional athletes around the world collapsing suddenly shortly after having gotten the shots. Israeli researchers found a list of 183 professional athletes or coaches who died suddenly this year, well beyond the normal baseline over the past 20 years. Most were very young, and 80 of them collapsed on the field. Most of the reported causes were heart-related, including myocarditis, pericarditis, heart attacks, or cardiac arrest, as well as blood clotting.
Again, if we are seeing this magnitude of disturbing safety signals and this degree of short-term deaths and injuries, what does that portend for long-term safety for millions of people? It’s one thing to not study long-term effects of a vaccine because of the imminence of a pandemic, and then we see no short-term safety problems. But now that we are experiencing an unprecedented number of short-term injuries, how can we assume this is safe long-term?
Republican leaders are happy that the courts are enjoining Biden’s federal mandate. This way they can wash their hands of having to fight against it politically in a way that will actually endure. The reality is that most large corporations will still impose the mandates because the government has removed the ultimate market-based check and balance against dangerous products by exempting the manufacturers from any liability, including for willful misconduct. This is why every Republican governor and legislature has an obligation to impose workplace injury liability on any employer that mandates the shots. They can’t have it both ways. If it’s truly safe and effective, they should have no problem applying the same standard of workplace injury liability we apply to all other workplace requirements imposed by employers.
When state legislatures convene in January, they have an obligation to pick up the slack on oversight of these shots. If they fail to do so, our Constitution will be replaced with the balance sheets of Pfizer.
I'm beyond sick and tired of this dog and pony bullshit parade that's been going on for over 2 years now... The crazy ass wack job that wasn't elected governor of my state just implemented a indoor mask mandate for all indoor businesses. Show proof of vaccination or be forced to wear a mask... Let's continue to shove the unproven "safe" "vaccine" down your throat. Masks don't work. The vaccine doesn't work. Look at Israel as a case study while other non pushed vaccine county's have low Covid numbers.. this world fucking sucks right now. "Slow" the spread has turned into population control of loss of rights, freedoms etc...any excuse to control a individual or try to shove this unproven science down your throat will be used.
Has any state tried to have a work day boycott of forced mask wearing mandates? Where workers in the state all call in a certain day and show there disapproval of the measure taken.
College is 99% vaxxed and now locked down.
https://thelibertydaily.com/more-pr...lege-locks-down-all-classes-over-covid-surge/
that makes a lot of sense tho.
if you want the human population to go down, force those on the verge of breeding to get a vaccine that causes a high rate of infertility and fetal injury.
Duh….
what are you a white supremacist trump voter? Fuckin misogynistic, racist piece of shit. Of course you’d be against culling the human population… I bet you drive a diesel truck too!!!
(I’m interviewing for a job at CNN, heard they were lookin for talent… am I doing good?)
humans used to live for hundreds of years, population is still growing thothat makes a lot of sense tho.
if you want the human population to go down, force those on the verge of breeding to get a vaccine that causes a high rate of infertility and fetal injury.
Duh….
what are you a white supremacist trump voter? Fuckin misogynistic, racist piece of shit. Of course you’d be against culling the human population… I bet you drive a diesel truck too!!!
(I’m interviewing for a job at CNN, heard they were lookin for talent… am I doing good?)
Compromised...
JUST IN - U.S. Supreme Court declines to block New York vaccine mandate for health care workers that does not allow religious exemptions.
MORE - This is the first landmark decision regarding compulsory vaccinations in the United States by SCOTUS. 3 dissents: Alito, Gorsuch, and Thomas. Roberts, Barrett, and Kavanaugh sided with the liberals.
Colleen Huber, NMD, February 21, 2021, updated March 23, 2021
https://www.primarydoctor.org/covidvaccine
Most of the links below are from medical journals, the FDA, CDC, and other entities that generally support vaccination, yet the information in this article shows how EXTREMELY RISKY the COVID-19 vaccines are.
Is the COVID vaccine experimental? Pfizer and Moderna make the COVID-19 vaccines in the US. The FDA granted “emergency use authorization” for these vaccines (herein “COVID injections,” because they are unlike conventional vaccines). Emergency use authorization is required by law to be made only if there are no effective treatments for COVID-19.
But are there effective COVID-19 treatments? 100s of studies done around the world have established, and repeatedly confirmed, fast, effective, well-tolerated treatments for COVID-19 that are in widespread use. I briefly summarize them here.
General risk vs benefit An emergency experimental vaccine cannot be assumed to be safer than a virus with a very high survival rate, such as COVID-19. The average survival rate for NO COVID treatment at all is 99.74%, and we have very successful treatments available, which should easily achieve universal survivability from COVID, if widely available. Where does 99.74% survival come from? Dr. John Ioannidis is the most widely cited scientist in the world. His estimate in June 2020 of a 0.26% infection fatality rate is now confirmed around the world. 100% - 0.26% = 99.74% average survival rate.
Does the COVID injection work? The COVID injection is not even known to stop the spread of COVID. Dr. Larry Corey, who oversees National Institutes of Health COVID-19 vaccine trials said on 11/20/20: “The studies aren’t designed to assess transmission. They don’t ask that question, and there’s really no information on this at this point in time.” https://www.medscape.com/viewarticle/941388.
The FDA confirms that the 1st vaccine dose correlates with increased COVID-19 infections. "Suspected COVID-19 cases that occurred within 7 days after any vaccination were 409 in the vaccine group vs 287 in the placebo group." This data comes from Pfizer itself. See p 42 of https://www.fda.gov/media/144245/download
What happened to the animals in the studies? This technology has been tried on animals, and in the animal studies done, all the animals died, not immediately from the injection, but months later, from other immune disorders, sepsis and/or cardiac failure.There has never been a long-term successful animal study using this technology. No experimental coronavirus vaccine has succeeded in animal studies. In this study, coronavirus vaccine caused liver inflammation in test animals.
Specific risks of COVID injections, in roughly chronological order of side-effect manifestation:
Polyethylene glycol (PEG) is one of the ingredients. This has been correlated with anaphylactic shock. So the CDC is now recommending intubation kits at vaccination sites.
Cationic lipid coating of mRNA is known for many years to be toxic, because these (+) charged fats interact with the (–) charges on our amino acids, our cell membranes and the phosphates of our DNA. Cationic lipids are attracted to and are destructive toward:
Lungs ,
Mitochondria,
red blood cells,
white blood cells,
Liver,
Immune and nervous systems function (This is the likely cause of the Bell’s Palsy and tremors that are seen in vaccine victims.)
mRNA: Unlike a traditional vaccine, of injected, inactivated virus intended to stimulate antibody response, the COVID injection on the other hand is completely different in this respect. It uses messenger RNA (mRNA), which is a blueprint for your cells to create COVID-like (spike) proteins. Then your cells begin to make these COVID-like proteins. However, those proteins, in turn, stimulate your body to make antibodies against them. So now your body has been turned into a munitions factory for both sides of a war: The bad guys (COVID-like spike proteins) and the good guys (the antibodies fighting against them). However, before you pledge allegiance to the good guys, as you will see below, the good guys can be more lethal to the vaccinated person.
History of mRNA injections: This technology had disastrous results in dengue fever vaccines in the past. Dengue vaccine is a mRNA vaccine. When this was used in children in the Philippines, many vaccinated children had far worse outcomes than unvaccinated children when they were later exposed to dengue, and many died. Prosecution for homicide resulted. However, this had previously been known to happen with ferrets and with cats. In all cases, the vaccinated animal or human became more vulnerable to worse disease when confronted with it. It is expected that the relatively mild COVID-19 illness, with a survival rate of 99.74%, may reduce to a much lower survival rate and become a truly lethal disease in vaccinated people when they later become infected with it.There are no peer-reviewed published human trials of mRNA vaccines at all, and no mRNA vaccine has ever been FDA approved. That’s how new the technology is.
mRNA can affect DNA. One of the most worrisome risks with a mRNA vaccine is what can happen with reverse transcriptase. This is an enzyme in every cell, and it can theoretically lead to the mRNA creating changes in the cells’ DNA, a process known as viral retro-integration. Although this possibility had been thought unlikely, MIT and Harvard scientists found it happened here. If some of the 30 trillion or so cells in your body become permanent COVID factories, what is the long-term impact on your health, and would you want that outcome?
Antibody dependent enhancement (ADE) problem: Prior attempts to create a coronavirus vaccine killed all the test animals, after they were later infected with wild virus. Here’s what happened: mRNA instructed the mammals’ cells to produce the spike proteins of the coronavirus. Then, later, when the animals confronted the wild virus, the intense build-up of antibodies had been stockpiled, and their sudden and overwhelming release killed the test animal. These risks have been documented in Nature, Science and Journal of Infectious Diseases. Here’s a study from Nature on that.
ADE mechanism: ADE is a form of pathogenic priming, meaning the vaccine can result in a more severe disease, which has been seen in prior attempts at making coronavirus vaccines. The antibodies made can be neutralizing (which inactivate a virus, and that’s good), but antibodies are a problem when they are non-neutralizing, because then these antibodies carry active viruses directly to macrophages, which then become infected. This is how ADE happens.
This antibody dependent enhancement (ADE) leads to:
increased viral replication (more viruses to make you sick); and more severe disease
ADE result: These macrophages tend to go to the lungs and fill the lungs, causing overwhelming inflammation and airway obstruction (as found later on autopsy). However, the augmented antibodies also attack similar-looking proteins on internal organs, resulting in cytokine storm and death or auto-immune disease and organ failure. “Cats that showed high titers following vaccination succumbed at later timepoints to fatal disease.”
What about miscarriages, and why have men been advised to freeze their sperm prior to getting the injection? Both men and women are at risk for possibly permanent infertility, because the spike protein of a coronavirus “looks” to the immune system similar to Syncytin-1, an essential protein in the placenta. This stimulates antibodies to fight the placenta, and possibly sperm. Mid-term miscarriages, which are normally very rare, have occurred in women who have been vaccinated for COVID. SARS-CoV-2 viral particles have been found to linger in the testicles of men after recovery from infection.
Why are COVID vaccinees MORE likely to spread COVID than the unvaccinated? Virologist Geert Vanden Bossche PhD, who worked for the Bill & Melinda Gates Foundation, recently warned the World Health Organization (WHO) that "We are currently turning vaccinees into carriers shedding infectious variants."
Why is it more dangerous to vaccinate against COVID-19 than other viruses? Because COVID-19 virus uses the ACE-2 receptor to get into your endothelial cells, including those lining the blood vessels. This creates an inflammatory reaction that the great majority (99.74%) have survived even without treatment, and even more who used known, effective treatments. (See page 1) So if you have been exposed to the virus, and then get vaccinated, it is almost certain that the vaccine will cause new inflammation and damage to endothelial cells lining your blood vessels, and we have seen short-term abnormal blood clotting in people who have gotten the vaccine. But the more likely problem is launching new disease in the blood vessels. Dr. H Noorchashm MD, PhD says, “. . . the vaccine is almost certain to do damage to the vascular endothelium.” He explains here.
Israel is at this writing the most heavily COVID-vaccinated country in the world. The findings of infectious disease experts are reported here, in which they determined, from the Israeli data, that the COVID injection causes:
" . . .mortality hundreds of times greater in young people compared to mortality from coronavirus without the vaccine, and dozens of times more in the elderly . . .”
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Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19
https://ijvtpr.com/index.php/IJVTPR/article/view/23/49
Potential for Permanent Incorporation of Spike Protein Gene into human DNA
'It has been claimed that mRNA-based vaccines are safer than DNA-vectored vaccines that work by incorporating the genetic code for the target antigenic protein into a DNA virus, because the RNA cannot become inadvertently incorporated into the human genome. However, it is not at all clear that this is true. The classic model of DNA → RNA → protein is now known to be false. It is now indisputable that there is a large class of viruses called retroviruses that carry genes that reverse transcribe RNA back into complementary DNA (cDNA).'
'In 1975, Howard Temin, Renato Dulbecco, and David Baltimore shared the Nobel Prize in Physiology or Medicine in 1975 for their discovery of reverse transcriptase and its synthesis by retroviruses (such as human immunodeficiency virus (HIV)) to derive DNA from RNA (Temin and Mizutani, 1970, Baltimore, 1970).'
'the mRNA in the new SARS-CoV-2 vaccines could also get passed on from generation to generation, with the help of LINEs expressed in sperm, vianon-integrated cDNA encapsulated in plasmids. The implications of this predictable phenomenon are unclear, but potentially far-reaching.'
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mRNA COVID-19 vaccines are really ‘gene therapy’ and not vaccines
former professor at the University of Virginia’s school of medicine Dr. David Martin, Ph.D
https://www.lifesitenews.com/news/m...really-gene-therapy-and-not-vaccines-ethicist
“The problem is that in the case of Moderna and Pfizer, this is not a vaccine. This is gene therapy,” he continued. The Moderna and Pfizer creations send “a strand of synthetic RNA into the human being and is invoking within the human being the creation of the S1 spike protein, which is a pathogen.”
“This is not only not keeping you from getting sick, it’s making your body produce the thing that makes you sick,” Martin added.
The interviewer admitted that this description – that the injection makes one's body produce an effect that makes one sick – sounds somewhat similar to the effect of vaccines.
But Martin countered that it is “not at all” like a vaccine, since “a vaccine is supposed to trigger immunity. It’s not supposed to trigger you to make a toxin.”
“It’s not somewhat different. It’s not the same at all,” Martin explained. “It’s a means by which your body is conscripted to make the toxin that then allegedly your body somehow gets used to dealing with, but unlike a vaccine, which is to trigger the immune response, this is to trigger the creation of the toxin.”
Targeting the pharmaceutical companies behind the supposed vaccinations, Martin alleged that they have manipulated clinical trial methodology to push their “vaccines” through development and production.
“They (pharmaceutical companies) said they could not test for the existence or absence of the virus and they could not test for the transmissivity because they said it would be impractical. (lol) The companies themselves have admitted to every single thing I’m saying, but they are using the public manipulation of the word vaccine to co-opt the public into believing they’re getting a thing which they are not getting.”
Instead, Martin warns that an mRNA injection “is not going to stop you from getting coronavirus. It’s not going to stop you from getting sick. In fact, on the contrary, it will make you sick far more often than the virus itself.”
Martin presented data confirming his claim, noting that after receiving their second shot of the jab, “80 percent of people had one or more clinical presentations of COVID-19,” whereas “80 percent of people who have an infection according to RT-PCR have no symptoms at all.”
Explaining what the figures mean, he said that people “will get COVID-19 symptoms from getting the gene therapy passed off as a vaccine. You will get COVID symptoms from that 80 percent of the time. If you’re exposed to SARS-CoV-2 according to RT-PCR (positive PCR test), 80 percent of the time you will have no symptoms at all.”
Looking more closely at the claims emanating from the clinical trials, Martin questioned the integrity of companies developing mRNA “gene therapy technology.”
“A human being is going to be potentially exposed to unclassified, both short-term and long-term, risks of altering their RNA and DNA from exposure to this gene therapy,” Martin warned. Of the 40,000 participants in Moderna’s clinical trial, Martin noted that only a “few hundred people had a few days less severe symptoms with the gene therapy when compared to the other control group.”
Even this, he said, is unreliable information, as the pharmaceutical firms “separate out adverse events from actual COVID symptoms.” This allowed the companies to reclassify “a lot of what would have been considered to be COVID symptoms by calling them adverse events,” giving rise to “this ridiculous 90 percent plus effectiveness.”
“As a result of that, we have both a methodology problem, which by the way, has been criticized by a number of clinical scientists. The bigger problem is that they’re still not measuring viral susceptibility and viral transmission. Those are the two legs of the stool that is (sic) required for anyone to say that they are vaccinating a population for public health reasons.”
Martin advised that “this (gene therapy) is not a prophylactic, this is not helping us, we are being told to take a treatment for a disease we don’t have and most likely will not have.”
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Corona Unmasked
select excerpts taken from prelim pre pub chapter of forthcoming, yet to b finalized book – 'Corona Unmasked' – authored by world renowned German-Thai-American microbiologist Dr. Sucharit Bhakdi (and some whore)
https://www.goldegg-verlag.com/goldegg-verlag/wp-content/uploads/corona_unmasked_engl_leseprobe.pdf
The vaccines are here, and they are being given en masse – yet we don’t know if they work, how well they work, or what they do. That is why these vaccines have not been given regular approval by the EU, but only a “conditional approval” for emergency use (1). In the next 2 years, it will be re-viewed whether their benefits outweigh the risks. Every person who gets vaccinated now is part of this huge experiment. But, of course, without any liability!
Because with vaccinations under emergency rules, the manufacturers make no guarantees whatsoever – in case of serious reactions, or even in case of death, they are free from any liability.
Especially for completely novel, gene-based vaccines such as the mRNA vaccines against CoroSARS-CoV-2, a careful study of the possible risks would be particularly important, because according to the current state of scientific knowledge, a variety of severe side effects are conceivable.
It is thus all the more astonishing that meaningful studies on the efficacy and safety of these novel vaccines do not exist at all - Nor were such studies feasible within the short time available. Three pharmaceutical companies were at the fore-front of the mad race for the highly lucrative emergency approval: AstraZeneca with its DNA vector vaccine based on an adenovirus, and Biontech/Pfizer as well as Moderna with their mRNA vaccines. On December 21, 2020, the EU Commission approved the Biontech/Pfi-zer vaccine, followed shortly thereafter on January 6 by approval of the Moderna vaccine; and on January 29, AstraZeneca received EU approval, too. While careful clinical testing of a new vaccine was previously known to take at least 7–10 years, the whole process has now been shortened to mere months. Could reliable data be on the table in such a short time, so that the public could weigh risk versus benefit? Of course not. Nevertheless, everything was accepted and bought sight unseen by the authorities in Europe.
Do current vaccines protect against severe SARS-CoV-2 infection?
As a matter of fact, a protective effect against severe and possibly life-threatening COVID-19 disease could not be shown in monkey models with any of the vaccines (3–5).
What do the human trials say?
Mainstream media jubilantly spread the press releases of the companies without ever asking any critical questions. Thus, from the media we learn that the protection afforded by the vaccines is simply great – with Biontech/Pfizer the level of protection is even 95 percent! That sounds great – bring on the vaccination! But how do these numbers come about, knowing that healthy people very rarely get life-threatening COVID -19?
In fact, among the 40,000+ test subjects of the Biontech/Pfizer study (7), just 170 COVID-19 “cases” occurred (about 0.4%). Of these, 8 occurred among the vaccinated (1x severe), whereas 162 in the unvaccinated control group. The 8 cases in the first group equal 5% of the 162 in the second – therefore, 95% protection!?
Considering this small number of cases overall, the evidence must be described as plainly ridiculous from a scientific point of view. Moreover: how did this study define a “COVID-19 case” in the first place? Aha: symptoms like cough, cold, hoarseness and a positive RT-PCR test, which is extremely unreliable, as everyone knows by now. So, what we have here is a vaccination that might possibly prevent cough, cold, hoarseness in 0.7% of the vaccinated. For this breathtaking achievement, hundreds of vaccinated people had to accept severe side effects, some of which led to hospitalization.
The situation is no better for the other vaccine manufacturers. Accordingly, Professor Peter Doshi, writing in the prestigious British Journal of Medicine, complains: “None of the studies currently underway are designed to detect a reduction in severe outcomes in terms of hospitalization, admission to intensive care units, or death.«
How great is the benefit of vaccination, especially for the group most at risk from the infection? No one knows. Thereby, the justification for the conditional approval is the demonstrated prevention of serious or even deadly events. The conditional approvals for all gene-based vaccines were thus made without any basis whatsoever.
The human trial continues, and everyone who is now enthusiastic about being vaccinated is taking part.
Does the vaccine prevent infection and thus the spread of the viruses?
A widely proclaimed goal of vaccination is not only to prevent COVID-19 disease in the vaccinated persons, but also to prevent the spread of the virus in the population. Already in kindergartens and elementary schools, children are taught that they could unknowingly kill their grandparents because they carry the viruses without being sick themselves. To prevent this, everyone should be vaccinated, including the children. Does this make sense – can a vaccination prevent an infection at all?
Let us start with the first question: does it make sense to try to prevent the spread of viruses that are of little danger to most people in order to supposedly protect a risk group?
When we do develop symptoms, this is a sign that the viruses have found a chance to become active, and also that our immune system has entered the battle. If there is no cough, cold, hoarseness, etc., it means that our body is keeping the viruses at bay from the start. The viral load that a person can release into the out-side world without symptoms is too small to endanger other people in public. Therefore, the plan to vaccinate the entire population is a delusional and insane undertaking.
Let us turn to question 2: could the vaccines prevent the spread of SARS-CoV-2 viruses at all? The RKI states that this question is completely unresolved so far (13). To find out, one would have to examine whether 1) vaccinated people can still get an infection and whether 2) in this case, the amount of virus present is sufficient to infect others.
AstraZeneca alone made headlines with the news that vaccinated people were significantly less contagious. However, on closer inspection, it is blindingly obvious that once more no data exist to draw this conclusion. The study in question only looked at part 1 of the question: how many more people get an infection after being vaccinated. How was this checked?
The only criterion was positive RT-PCR tests (14). Now even the WHO says that the PCR test alone is not enough to diagnose an infection (15). So what is the the unsubstantiated claim worth that the spread of infection was massively reduced by the AstraZeneca vaccine? NOTHING.
Anyone who has the slightest idea about infections and immune defense also knows that the mechanistic concept for the SARS-CoV-2 vaccination which is presented to the public is amateurish and naive from the start. The antibodies induced by the vaccination will circulate for the most part in the bloodstream. For an analogy, readers may imagine that they themselves are such antibodies, sitting together in the living room – which represents a blood vessel of the lungs. Now the virus comes to the house – not bothering to ring the bell, it just grabs the door handle and steps into the hallway: the lung cell. How could you possibly stop it from doing so, while sitting in the living room? You can’t.
Antibodies can basically only help prevent the further spread of an intruder through the bloodstream. But that is not the primary protection against an attack from the air against the lungs. And that is precisely why there is no truly effective vaccine protection against respiratory infections, including influenza.
If the benefits of vaccinations are more than questionable, what about the risks?
We read in the mainstream media: mRNA vaccines are not new after all. That is true, but they have NEVER been used on humans to fight a viral infection. And humans have never been inoculated with recombinant viral genes, in the form of either DNA or mRNA.
Accordingly, the vaccinations were under a dark cloud from the outset. With all three gene-based vaccines, disturbing immediate side effects were noted – but carefully hidden from general awareness: severe swelling and pain at the injection site, high fever and chills, severe headache, limb and muscle pain throughout the body, diarrhea, nausea, vomiting. Many vaccinated people were so sick that they were unable to work. In the AstraZeneca study, the side effects were so bad that the study protocol had to be changed halfway through: in the later stages, study participants received high doses of the pain- and fever-relieving drug aceta-minophen in order to make the vaccination reasonably tolerable (16). Such changes of protocol in the middle of a study are actually not permitted at all. Why was an exception made here?
But that is not all. The AstraZeneca study was interrupted in July and September 2020 because of the occurrence in vaccinees of an extremely rare autoimmune disease, which affects the spinal cord (17). “Transverse myelitis” is associated with paralysis and normally occurs at the very low frequency of approximately 3 per 1 million population, every year. It is surprising,
then, that 2 such cases occurred among a relatively small number of vaccinated individuals. AstraZeneca announced days later: calm down people, the first test person had incipient multiple sclerosis, the second case was purely an unfortunate coincidence. The show will go on! And so it did – AstraZeneca continued to forge ahead. But not only AstraZeneca – so did everyone else.
Comparable events occurred with competitors Mo-derna and Biontech/Pfizer. With both vaccines, volunteers suffered similarly severe general side effects. This sentence might be moved up to the discussion of general febrile reactions to the AstraZeneca vaccine.
Such a variety of immediate side effects has never been observed with any other vaccination. In America, when comparing the number of reported side effects of different vaccines over the 2 last years, the COVID-19 vaccine already comes out on top, although it was approved only in December 2020 (19).
Is the mRNA vaccine dangerous?
«No« is the answer that is spread everywhere. This is because 1) the vaccine introduces into our body only the information for a small part of the virus, for the so-called spike protein, which means that there is no intact virus that could propagate, and 2) the vaccine only imitates what Nature, too, would do. Intact viruses also release their genetic material into our cells when they attack, turning our cells into virus factories. So, no problem there at all, right?
Far from it. A natural respiratory infection typically affects only the respiratory tract itself. If, at worst, cell death occurs, the damage is local and can be repaired relatively easily.
With a vaccine, however, the viral genetic information is injected into the muscle. Many believe that the packaged viral genes remain at the site of injection – that is, within in the muscle. The genes would be taken up by cells at the site, which is where most “virus factories” would be created. Side effects such as swelling, redness and pain at the injection site would be expected because of this, but they would remain relatively harm-less and go away after a few days.
What a fatal mistake!
The virus genes in the Moderna and Biontech/Pfi-zer vaccines are packaged in so-called nanoparticles – which can be thought of as tiny packages, not made of paper, but of fat-like substances. This protects the contents and makes it easier for them to be absorbed by the cells of our body. The packaging itself causes a risk of severe allergic reactions that is many times higher than with conventional vaccines (20). It is thus not without reason that people with allergies are now being warned not to get vaccinated – life-threatening reactions (anaphylactic shock) could be triggered. In fact, such dangerous side effects did occur in some vaccination volunteers, who required emergency treatment. In addition, nanoparticles can have numerous other harmful effects because they can interfere with the function of our blood cells and clotting system (21).
But it gets infinitely worse. It is part of basic medical knowledge that all soluble substances injected into muscle tissue enter the bloodstream and are distributed throughout the body within a very short time. This is precisely why substances that are supposed to act immediately are injected into the muscles.
It is known that the injected gene packets also enter the bloodstream (22). Which cell types will take them up, process them, and then produce the virus protein?
The answer to this is not known with certainty.
We are now witnessing large-scale experiments on humans. This is absolutely irresponsible, especially since there was reason for caution from the beginning. The potential dangers from the “packaging” were already known. More significantly, however, alarming antibody-dependent enhancement – in this case, the antibodies do not prevent uptake of the virus into cells, but rather enhance it – has been observed in animal studies on SARS and other coronaviruses (23, 24). In the decades-long, yet futile effort to develop vaccines against SARS or MERS, this enhancement effect was repeatedly observed, as one among problem among many others (25). With this in mind, should not animal studies have been conducted to clearly rule out this effect for SARS-CoV-2? Physicians who do not alert those willing to be vaccinated to the risk that vaccination could make the disease worse, not better, are in violation of their duty to inform (26).
And more seriously, could the inoculation of viral genes trigger other novel immune-related enhancement effects? Shouldn’t such very elementary things have been considered and tested beforehand?
As a reminder, lymphocytes have a long-term memory – they remember what the «molecular garbage« looks like that is produced in Coronavirus infections. And corona garbage looks pretty much the same no matter which member of the virus family it is derived from. All humans have had training rounds with coronaviruses, and thus they have lymphocytes that will recognize SARS-CoV-2 garbage. People without in-depth knowledge might counter that these cross-reactive killer lymphocytes were detected in only 40–70% of old blood samples, and they reacted only weakly against SARS-CoV-2 (27, 28). However, it is known that only a small proportion of all lymphocytes are in the blood at any given time. The others are just taking a break and resting in the lymphoid organs (including the lymph nodes).
Here, we note an exciting finding: In April 2020, Swedish researchers reported that they had discovered something truly remarkable. Activated and combat-ready T lymphocytes were found in the blood of all people (100%) infected with SARS-CoV-2, regardless of the severity of the disease (29).
This finding is a clear, unmistakable warning.
For context: during an initial confrontation of the immune system with a virus, the lymphocyte response will be sluggish. Rapid, strong reactions such as that documented by the Swedish team reveal that forewarned troops are already at the ready and can be mobilized on short notice. They will swarm out of the lymphoid organs to fight the enemy. Their main task: extermination of the virus factories – death to the body’s own cells that produce the virus particles.
And now back to the new reality: the large-scale experiment on humans. The injected gene packets are taken up locally in muscle cells, but a large part reaches first the local lymph nodes and, after passing through these, the bloodstream. The lymph nodes are where the immune cell team resides. When the viral gene is taken up by any cell there, production of the spike protein gets underway. The corona killer lymphocyte next door wakes up and springs into action – the brotherly battle begins! Lymph node swelling. Pain. The lymphocytes psyche each other up and then emerge from the lymph nodes to seek out more enemies.
Yes – over there – the muscle cells! There they are!!! Attack!!! At the injection site redness, swelling, bad pain.
But now the nightmare.
This is because the substances with small molecules – for example, blood sugar – can easily seep out of the blood into the tissue, whereas large molecules such as proteins cannot. For them, the vessel walls are tight thanks to the lining with a cell layer – the endothelial cells.
What are the gene packages like – large or small?
Right – compared to blood sugar, they certainly are large. Therefore, once they enter the bloodstream, they will remain in the closed network of vascular tubes just like the blood cells. A small part of them is taken up by white blood cells. Presumably, however, most of the virus factories will be established in the endothelial cells, that is, in the innermost cell layer of the blood vessels themselves. This would happen mainly where the blood flows slowly – within the smallest and smallest vessels – because the gene packages can be taken up particularly efficiently by the cells there (30).
The endothelial cells then produce the viral spike protein and place the waste at the door – on the side that faces the bloodstream, where killer lymphocytes are on patrol. This time, the fight is one-sided. The endothelial cells have no defense.
What happens then can only be guessed at. Injury to the vascular lining usually leads to the formation of blood clots. This would likely happen in countless vessels in countless places in the body. If it happens in the placenta, severe damage to the child in the womb could result.
Shudder.
Is there evidence that something like this is taking place? Yes, there is talk of rare blood disorders in which a possible link to vaccination would have to be investigated (31). Strikingly, there are reports of patients in whom a sharp drop in blood platelets (thrombocytes) was observed. This would fit the hypothesis put for-ward here, because platelets are activated and used up at the sites of blood clot formation.
What is more, it seems that particularly the vaccinated are dying. Is this perhaps the immune-related exacerbation of diseases we have reason to fear? Not caused by antibodies, but by activated killer lymphocytes? And couldn’t this happen at any time to anyone vaccinated – tomorrow, the next day, next week, next fall? Because lymphocytes have an elephant’s memory. And they recognize something that looks similar in all coronaviruses: the molecular garbage that is produced by the virus-infected cells. That is, the lymphocyte induced exacerbation of disease progression could arguably occur with any infection with a related virus. In any “successfully” vaccinated person – young or old – and at any time in the near or distant future.
Conclusion
Gene-based vaccines received emergency approval at lightning speed to combat a virus that is no more dangerous than influenza (34). There is now clear evidence that people can become severely ill and die from these vaccinations. No real-world benefit of vaccination has ever been shown. Until reliable and convincing data are available, this high-risk human experiment must not be allowed to continue.
Compromised...
JUST IN - U.S. Supreme Court declines to block New York vaccine mandate for health care workers that does not allow religious exemptions.
MORE - This is the first landmark decision regarding compulsory vaccinations in the United States by SCOTUS. 3 dissents: Alito, Gorsuch, and Thomas. Roberts, Barrett, and Kavanaugh sided with the liberals.
Wonder what affect this decision will have for the rest of the country and private employers.
"religious exemption" is a farce and just verbage put to paper. Look at the NBA, the actor from the soap opera and so on. Every single attempt to get the exemption has been denied.
cOiNcIdEnCe
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