[Government is Trying to Kill You] 45 Times as Many Deaths After COVID Shots in Just 2 Years Compared With All Flu Vaccine-Related Deaths Since 1990, Data Show

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From [CHD] The cost of injecting healthy people, “especially children,” with a Pfizer or Moderna COVID-19 vaccine “outweighs any claimed though unvalidated benefits,” according to researchers who analyzed adverse events data from more than 10 regulatory surveillance and self-reporting systems during the first two years of the COVID-19 vaccine rollout.

“Our meta-analysis of both national and international vaccine adverse events emphasizes the importance of re-evaluating public health policies that promote universal mass injection and multiple boosters for all demographic groups,” said the authors of a peer-reviewed studypublished this month in the International Journal of Vaccine Theory, Practice, and Research.

Eliana Romero, Ph.D., director of clinical research at the Neurodiversity Foundation, Shawn Fry, founder and chief science officer of the Neurodiversity Foundation and Brian Hooker, Ph.D., P.E., chief scientific officer of Children’s Health Defense and associate professor of biology at Simpson University in Redding, California, authored the paper.

The researchers looked at adverse events specifically related to cardiovascular and fertility health — such as myocarditis and menstrual abnormalities — that went overlooked during the “expedited safety analyses” that took place in the “accelerated approval process that allowed the manufacturers to fast-track their products,” they said.

They analyzed data from the Vaccine Adverse Event Reporting System (VAERS) database — the primary government-funded system for reporting adverse vaccine reactions in the U.S., which has been shown to report only 1% of actual vaccine adverse events — and the Defense Medical Epidemiology Database (DMED), the medical events database for all active and reserve U.S. military.

The authors also examined data from other regulatory surveillance and self-reporting systems including the V-safe After Vaccination Health Checker, the U.K.’s Yellow Card reporting system, Public Health Scotland, the Israeli Ministry of Health and the Natural Cycles App.

Hooker said the data highlights “the dramatic uptick in adverse events associated with the COVID-19 vaccine.”

After carefully conducting statistical analyses, the authors concluded there were far more reports of adverse events following COVID-19 vaccination than following either influenza or pertussis vaccination.

The researchers also found “statistically significant higher numbers of hospital encounters in military personnel” after the COVID-19 vaccine rollout when compared to just before the rollout, and “increases in incidences of thromboembolic conditions, such as menstrual abnormalities, myocarditis, and cerebrovascular events after the implementation of COVID injection mandates, compared to the preceding five years.”

The researchers verified their conclusions by comparing their findings to similar reports from other regulatory surveillance and self-reporting systems including EudraVigilance, Eurostat, German health insurers and the U.K.’s Office for National Statistics.

In addition to statistically significant increases in vaccine adverse events, the data showed “highly statistically significant” increases in “specific morbidity” and “all-cause mortality,” Hooker told The Defender.

“These results should not be ignored,” he added.

More than 45 times as many deaths after COVID shots than all flu vaccine deaths combined since 1990

The researchers found the number of reported deaths related to an mRNA COVID-19 vaccine was more than 45 times as many deaths per vaccine dose as were reported for all the influenza vaccines combined since 1990.

They also found a higher incidence of menstruation problems, myocarditis and cerebrovascular events following COVID-19 vaccination than following influenza vaccination, as seen in figure 1A:

The researchers also compared adverse events reported in VAERS following the COVID-19 vaccines to adverse events reported following the influenza and pertussis vaccines.

They showed the percentage of total reports attributed to death, for the COVID-19, influenza and pertussis vaccines, as seen in figure 1B:

Should the trends in myocarditis rates continue, “we will see spikes in death rates attributed to the increase in myocarditis documented above, as well as in the number of otherwise healthy young adults needing transplants to survive, and all the complications associated with such a transplant,” the authors said.

DMED data trends mirrored VAERS and other surveillance data trends, which showed dramatic increases in many medical conditions in 2021 after the COVID-19 vaccine rollout when compared to the previous five years.

The researchers also pointed out that on Feb. 1, 2022, Sen. Ron Johnson (R-Wis.) wrote a letter to U.S. Secretary of Defense Lloyd J. Austin III asking if the U.S. Department of Defense (DOD) was aware of the DMED data.

“If so,” Johnson said in his letter, “please explain what actions DOD has taken to investigate the root cause for the increases in these diagnoses.”

COVID vaccines not as ‘benign’ as the media said they were

Romero, the paper’s lead author, said the research wasn’t done “for a cause” or “with any predetermined hope for any specific results.”

Romero said she initially “had no qualms” about taking the COVID-19 vaccine, but soon it became “impossible not to hear all the opposition to them and, always a researcher at heart, I decided to follow up.”

Romero holds a doctorate in molecular and human genetics and has worked with some of the world’s top neurogeneticists.

“I’m a scientist through and through,” Romero told The Defender. “I also have Asperger’s, so I’m not exactly wired to tell anything but the truth.”

Romero began finding “mounting evidence the vaccines weren’t as benign as the media was desperately trying to convince us they were,” she said and felt an obligation to share what she was finding with others.

Romero — who has 20 years of experience investigating the genetic and biological aspects of various disease states at Baylor College of Medicine, Children’s Hospital of Pennsylvania, Johns Hopkins University and several private laboratories — said she used “all avenues available” and “went through every effort to standardize my data, compare apples to apples, and to perform any calculations I knew of to test the validity of the data presented.”

“The paper isn’t an attempt to skew anybody’s opinions one way or the other,” Romero emphasized. “Its sole purpose is to make sure people have all the information they need to make the best decisions they can for their health,” she said.

“Governments and institutions and scientists and doctors should provide people ALL the information needed so that individuals can make truly informed decisions for themselves.”

Are You Eating Pork Injected With Merck’s mRNA Livestock Vaccine?

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Story at a glance:

  • For the last couple of years, I’ve recommended not eating pork due to its high linoleic acid (LA) content, but there’s an even bigger reason to avoid it now. Since 2018, pork producers have been using customizable mRNA-based “vaccines” on their herds.

  • The very first RNA-based livestock vaccine, a swine influenza (H3N2) RNA shot licensed in 2012, was developed by Harrisvaccines. The company followed up with an avian influenza mRNA shot in 2015. Harrisvaccines was acquired by Merck Animal Health later that year.

  • CureVac developed an mRNA-based rabies shot for pigs in 2016.

  • The swine vaccine platform Sequivity, introduced in 2018, was developed by Merck in partnership with Moderna. Sequivity can produce endlessly customized “vaccines,” none of which undergo safety testing.

  • Americans have been eating pork treated with gene therapy for nearly five years already, and even more of our meat supply is about to get the same treatment. mRNA-lipid nanoparticle shots for avian influenza are in the works, as are mRNA shots for cows. Lobbyists for the Cattlemen’s Association recently confirmed they intend to use mRNA “vaccines” in cattle, which might affect both dairy and beef.

  • Missouri House Bill 1169 would require labeling of products that can alter your genes. It would also require companies to share information about the potential transmissibility of gene-altering interventions, and asserts that fully informed consent must be given for all vaccines, gene therapies and medical interventions.

From [HERE] For the last couple of years, I’ve recommended not eating pork due to its high linoleic acid (LA) content, but there’s an even bigger reason to avoid it now.

Since 2018, pork producers have been using customizable mRNA-based “vaccines” on their herds, and this has slipped completely under the radar. I myself just found out about it.

As described on Merck’s animal health website:

“A revolutionary swine vaccine platform, SEQUIVITY harnesses RNA particle technology to create customized prescription vaccines against strains of influenza A virus in swine, porcine circovirus (PCV), rotavirus and beyond. It’s supported by a sophisticated dashboard filled with comprehensive data and insights …

“Sequivity is a custom swine vaccine platform … Sequivity only targets swine pathogen gene sequences of interest. Doesn’t replicate or cause disease, delivering pathogen information to the immune system … There’s no need to transfer or handle live material like autogenous, killed or modified live vaccines …

“Targets existing and evolving swine pathogens, including diseases not covered by conventional swine vaccines. Allows for the creation of multivalent formulations by blending RNA particles to target multiple swine pathogens in one shot.”

First RNA ‘vaccine’ for livestock licensed in 2012

Merck was not alone in developing veterinary mRNA shots, however. They weren’t even first on the scene, although they later acquired the company that started it all.

The very first RNA-based livestock vaccine, a swine influenza (H3N2) RNA shot, was licensed over a decade ago in 2012, and was developed by Harrisvaccines. The company followed up with an avian influenza mRNA shot in 2015. Harrisvaccines was acquired by Merck Animal Health later that year.

CureVac developed an mRNA-based rabies shot for pigs in 2016. (On a side note, they began conducting human rabies shot trials in 2020 in response to the World Health Organization’s goal to achieve “zero human rabies deaths by 2030.”)

In 2016, Bayer also partnered with BioNTech to develop mRNA “vaccines” for both livestock and pets, but it doesn’t appear they ever launched anything.

So, in retrospect, it appears Americans have been eating pork treated with gene therapy for the past five years, and even more of our meat supply is about to get contaminated with the same treatment.

In addition to the avian influenza RNA shot for chickens licensed in 2015, newer mRNA-lipid nanoparticle shots for avian influenza are also in the works.

Iowa State University is also working on an mRNA shot for cows, and lobbyists for the Cattlemen’s Association recently confirmed they intend to use mRNA “vaccines” in cattle, which might affect both dairy and beef.

Merck and Moderna: Partners in mRNA jab race since 2015

The same year Merck purchased Harrisvaccines (2015), it also entered into a partnership with Moderna to develop a number of undisclosed mRNA “vaccines.” It was slated to be a three-year collaboration, with a one-year optional extension, in which Merck would perform research and development and commercialization of five potential products using Moderna’s mRNA technology.

As reported by Genetic Engineering & Biotechnology News at the time:

“Moderna has agreed to design and synthesize the mRNA product candidates directed against selected targets through its mRNA Therapeutics™ platform.

“The platform builds on the discovery that modified mRNA can direct the body’s cellular machinery to produce nearly any protein of interest — ranging from native proteins to antibodies and other entirely novel protein constructs with therapeutic activity inside and outside of cells.”

Endless customization, zero safety testing

Sequivity, introduced in 2018, was one of the products that came out of that partnership. As explained by Merck (both on its website and in the video below), Sequivity is not so much a single vaccine as it is a platform that can be endlessly customized — all without additional safety analyses over and beyond the initial ridiculously inadequate testing.

As noted by Zoetis, the largest producer of veterinary drugs and vaccines:

“Sequivity has safety and efficacy studies based on the platform with a historical initial isolate, not likely the isolate that customers would be requesting in their product.”

Sequivity is customized as follows:

  1. Pathogen is collected and sent to a diagnostic lab.

  2. The gene of interest is sequenced and sent electronically to Sequivity analysts.

  3. A synthetic version of the gene of interest is synthesized and inserted into the RNA production platform.

  4. The RNA particles released from incubated production cells are harvested and formulated into a customized “vaccine.”

Using this platform, a customized “vaccine” can be created in as little as eight weeks. Now, what could go wrong by not testing every new shot for safety? [MORE]

A Study by a Leading Expert in Sequencing Methods for DNA and RNA finds that COVID mRNA Shots Contain Excessive Quantities of Bacterial DNA that Cause Severe Health Risks

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by Michael Palmer, MD and Jonathan Gilthorpe, PhD

From [HERE] Recent studies by Kevin McKernan, a leading expert in sequencing methods for DNA and RNA, have revealed that batches of the modified mRNA vaccines produced by both Pfizer and Moderna contain a high proportion of contaminating bacterial DNA. In all, the DNA accounts for up to 20-35% of the nucleic acids contained in each of the vaccine batches. These alarmingly high concentrations far exceed the levels deemed safe by standard-setting organizations such as the European Medicines Agency (EMA). This document summarizes the evidence of that DNA contamination and discusses what possible health risks it implies to the recipients of the vaccines.

1. The role of DNA in the manufacture of mRNA vaccines

1.1. General background

Most readers will be aware that

  1. the synthetic RNAs contained in the COVID-19 mRNA vaccines encode the SARS-CoV-2 spike protein;

  2. in living mammalian cells, the instructions for building a given protein molecule are stored as a gene within the DNA inside the nucleus;

  3. to build a given protein molecule, the cell first transcribes its gene into RNA and modifies the two ends of this molecule to form messenger RNA (mRNA). The mRNA is then transported from the nucleus to the cytoplasm, where it induces the cell’s protein factories—the ribosomes—to translate the mRNA’s nucleotide sequence into the corresponding amino acid sequence and assemble the protein.

1.2. Steps in the manufacture of mRNA vaccines

Since the spike protein is a large molecule, so is the mRNA which encodes it. The total chemical synthesis of large mRNA molecules is not practical at scale. Therefore, in order to obtain the mRNA molecule encoding spike, the process by which cells produce their own mRNAs is mimicked in vitro. This involves the following steps:

  1. A DNA copy of the gene for the spike protein is inserted into a bacterial plasmid. This is a ring-shaped, double-stranded DNA molecule which can exist in a bacterial cell independently of the cell’s own chromosomal DNA, and which can also be copied and passed on to both daughter cells when that cell divides.

  2. The recombinant (artificial) plasmid carrying the spike protein gene is introduced into a cell of the bacterial species Escherichia coli (E. coli ). Since E. coli cells divide very rapidly, this one cell can within a short time be grown up to a very large number of cells. Each of these progeny cells will contain their own inherited copies of the plasmid, and therefore of the spike protein gene.While there is a certain chance of the plasmid being lost from some of the offspring during successive cell divisions, we can enforce its maintenance by giving it a selectable marker, which ensures that only those cells which retain the plasmid will survive. With the plasmids used by both Pfizer and Moderna, this selection marker is a gene which endows the host cells with resistance to the antibiotic kanamycin. To apply the selection, the bacteria are simply grown in the presence of kanamycin.

  3. After growing up a sufficient number of bacterial cells in a nutrient broth containing kanamycin, these cells are broken up and the plasmid DNA is purified from the other bacterial cell components.

  4. The ring-shaped plasmid molecules are converted to linear form using a restriction enzyme, which cleaves both strands of the DNA molecule at a specific, unique site which is located downstream of the spike protein gene. This step is needed to prevent the formation of RNA molecules that are overly long and might have undesired effects in vivo.The linearized DNA molecules can be purified from remaining circular ones, but in what manner and how efficiently this may be done in the production of Pfizer’s and Moderna’s vaccines is not public knowledge.

  5. An RNA polymerase is used, in the presence of the necessary nucleoside building blocks and cofactors, to copy the spike protein gene from the DNA version on the linearized plasmid into the mRNA version. Both Pfizer and Moderna employ the T7 RNA polymerase, which is derived from the eponymous bacteriophage. This enzyme binds to a cognate promotersequence likewise derived from T7 that has been engineered into the plasmid upstream of the gene for the spike protein. This interaction between polymerase and promoter initiates the transcription.At this stage, the synthetic nucleoside N-methyl-pseudouridine (mψU) is incorporated into the artificial RNA instead of the natural uridine nucleoside. When delivered in the form of a vaccine, RNA modified in this manner is less stimulatory to the innate immune system than is RNA containing the natural uridine. It is also more efficiently translated into protein, and under certain conditions more resistant to degradation [1]. Both Pfizer’s and Moderna’s mRNA vaccines contain mψU instead of uridine.

  6. The two ends of each RNA molecule are coupled enzymatically to certain moieties that are also found at these positions within natural mammalian mRNAs, and which enhance its biological activity and stability in vivo.

This steps provide a functional mRNA which is capable of instructing the cells’ ribosomes to produce the spike protein. However, at this stage the product is not yet pure—all of the bacterially derived template DNA is still present. The latter should not be included in the final drug product, because it poses health risks to the recipients (see Section 4). To get rid of this DNA, another enzyme called DNase is added. This should break up the DNA into smaller fragments, which can then be removed from the much larger RNA molecules by filtration and other purification techniques. In the final step, the mRNA is combined with a lipid mixture in order to package it into lipid nanoparticles (LNPs), which induce human cells to take up the mRNA molecule and to make the spike protein.

2. What did we know previously about the DNA contamination problem?

In a nutshell, very little. The FDA’s assessment reports on both vaccines [2,3] do not mention the issue at all. The European Medicines Agency (EMA) assessment report on the Pfizer vaccine mentions that “The robustness of the DNase digestion step is not considered comprehensively demonstrated” [4, p. 17]. Similar language is used in the EMA report on the Moderna vaccine [5, p. 19f]. However, based on this sparse information alone, it is impossible to say whether the problem was considered serious, and what remedies were required by the regulator, if any.

3. Independent evidence about DNA contamination of mRNA products

As of April 3, 2023, Kevin McKernan has described his recent findings in three articles on his Substack site [6–8]. The experiments described in the first two reports were carried out on samples of newly introduced “bivalent” vaccines from Pfizer and Moderna. These preparations resemble the previous “monovalent” ones in their chemical composition, i.e. they should contain highly pure mRNA, complexed with a mixture of lipid (fat-like) molecules into mRNA /lipid nanoparticles. The only difference between the two varieties is that the bivalent vaccines contain a mixture of two mRNAs encoding two antigenic variants of the spike protein. This has no bearing on the technical problem of DNA contamination as such. We note, however, that the extent of DNA contamination may vary between production batches, and that only a small number of batches has so far been characterized in this regard.

3.1. McKernan’s first report

In an initial study [6], McKernan characterized both the RNA and the DNA contained in the mRNA vaccines.

3.1.1. Extraction and direct characterization of nucleic acids from the vaccines

The first step consisted in stripping away the lipids in order to obtain the pure nucleic acids. The solvent-based method that he used does not discriminate between DNA and RNA—if both are present, both will be recovered. The extracted nucleic acids were separated according to size. This revealed not only the expected regular, full-length spike mRNA species, but also smaller fragments, which had been noted previously both by the regulators and in work published by one of the manufacturers [9]. More surprisingly, RNA species larger than the full-length mRNA were also found. These species remain uncharacterized.

3.1.2. Amplification of the extracted nucleic acids

As a preparatory step for determining the exact nucleotide sequences of the extracted nucleic acids, they were amplified by PCR methods. In the case of the RNA, PCR was preceded by reverse transcription into DNA using a dedicated enzyme (reverse transcriptase). Since this study’s primary goal was to study the RNA rather than the DNA, this amplification step was biased against DNA through the addition of actinomycin D, which under the given experimental conditions selectively inhibits DNA synthesis. Accordingly, relatively low amounts of DNA were recovered in the amplified sample. Nevertheless, in case of the Pfizer vaccine, the amount of DNA determined to be present already exceeded EMA’s arbitrarily decided limit for the maximal permissible proportion of DNA per RNA.

3.1.3. DNA sequencing results

With both Pfizer’s and Moderna’s products, DNA sequences of complete DNA plasmids were obtained, although some ambiguity remained in the case of the Moderna plasmids. The features of the plasmid sequences will therefore be discussed in connection with McKernan’s second study, which used more and more pure DNA for sequencing and therefore provided more reliable results.

3.2. McKernan’s second report

The second study [7] focused on quantifying and characterizing the DNA contamination that was qualitatively detected in the first one.

3.2.1. Plasmid DNA contained in the mRNA vaccines is competent to propagate in bacterial cells

In the first experiment, it was determined whether the plasmid DNA whose presence had been inferred from the previous sequencing results is indeed biologically functional, to the extent that it can be introduced into and persist within bacterial cells. To this end, nucleic acids were again extracted from the vaccine samples. These nucleic acids were mixed with a suspension of E. coli cells that had been rendered competent for DNA uptake.

After inducing these cells to take up the DNA and giving them some time to recover, they were spread onto Petri dishes filled with solidified growth medium containing kanamycin. As noted earlier, kanamycin will kill any E. coli cells that do not contain a resistance gene to it. Therefore, the observed growth of bacterial colonies on those Petri dishes confirmed that some cells had indeed acquired resistance to kanamycin by taking up and propagating the plasmids. This was observed with both the Pfizer and the Moderna vaccine samples.

In this context, we should note that only circular plasmid molecules, but not linearized ones, can be efficiently introduced into bacterial cells. The success of this experiment therefore suggests that some of the plasmid molecules had escaped the linearization step (step 4 in Section 1.2) and made it all the way through the production process in the circular form which exists in bacterial cells. On the other hand, since the number of bacterial colonies observed in this experiment was not high, it is likely that most of the DNA had indeed been linearized. Because the biological hazards of foreign DNA within our own body may vary depending on whether it is linear or circular, the likely presence of both forms in the vaccines is worth noting. The exact proportions of circular and linear DNA in the mixtures remain to be determined.

3.2.2. The abundance of contaminating DNA

The second major finding of this study is the quantitation by PCR of both DNA and mRNA contained in the vaccine samples. As you may be aware, in a PCR reaction, a chosen segment of a nucleic acid sequence is reduplicated by enzymatic synthesis in several successive reaction cycles. From the number of cycles (or doublings) necessary to reach a certain threshold concentration, we can calculate how many copies of the target sequence were present at the outset.

In these experiments, the chosen experimental format was multiplex PCR, i.e. two target sequences were amplified in a single reaction mixture. One of these targets was within the spike protein gene, and it thus should be present both on the plasmid DNA molecules and on the spike mRNA molecules transcribed from them. In order to include the mRNA molecules in this amplification, PCR was again preceded by reverse transcription.

The other target sequence was within the kanamycin resistance gene, which should be present only on the plasmid DNA. By comparing the number of cycles required for each of the two targets to cross the threshold, it was determined that up to 35% of the total nucleic acid contained in the vaccines is in fact DNA. For comparison, the EMA has stipulated that DNA should not amount to more than 0.033% of the total nucleic acids.

3.2.3. Determination of plasmid DNA sequences

The plasmids that had originally been contained in the vaccines and then been introduced into bacterial cells (see Section 3.2.1) were again isolated from those bacterial cultures, and their complete DNA sequences were determined. Such sequences were provided in full in McKernan’s first study [6], but he indicated that he was still working on corroborating and refining the sequencing data. Meanwhile, the functional features of the plasmid DNA found in the Pfizer vaccine samples are shown in Figure 1. They will be discussed in connection with the risk assessment.

The 2022 US Vaccine Damage Report says COVID Injections Have Caused 300,000 Deaths, 26.6 Million Injuries and 1.36 Million Disabilities. Shots Increase Risk of Myocarditis, Lead to Neurological Harm

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From [HERE] and [PDF] STORY AT-A-GLANCE

  • The 2022 U.S. Vaccine Damage Report revealed a sobering glimpse into the true carnage that occurred at the hands of the COVID-19 shot campaign

  • COVID-19 shots resulted in 300,000 excess deaths, 26.6 million injuries and 1.36 million disabilities

  • Total economic costs due to the shots are estimated at $147.8 billion, including $89.9 billion from related injuries, $52.2 billion from disabilities and $5.6 billion from excess deaths

  • A preprint systematic review found the mRNA-based COVID shots increased the risk of myocarditis, with a mortality of about 1 to 2 per 200 cases

  • Evidence of serious neurological harms, including Bell’s palsy, Guillain-Barré syndrome, myasthenic disorder and stroke, which are likely due to an autoimmune reaction, was also found from the shots

We're beginning to see the fallout from the mass COVID-19 shot campaign, which has been referred to as the "greatest violation of medical ethics in the history of medicine, maybe humanity."1

Former BlackRock analyst and fund manager Edward Dowd is one of the few trying to get the word out about COVID-19 shot risks, and he's been using data and statistics to prove his point and publicize the undeniable increase in deaths and disability among young, healthy adults that has occurred since the shots' widespread rollout.2

This group — the 148 million employed Americans between the ages of 18 and 643 — is typically a healthy crowd. This is why private insurance companies love to sell group life insurance policies to large Fortune 500 corporations and mid-sized companies —they hardly ever have to pay out on a claim. But this is changing.

Dowd's 2022 U.S. Vaccine Damage Report4 revealed a sobering glimpse into the true carnage that occurred at the hands of the COVID-19 shot campaign, and its results are striking.

300K Excess Deaths, Millions of Injuries, Billions in Costs

Dowd and colleagues published their 2022 Vaccine Damage Project at their website, Phinance Technologies.5 It revealed the following estimated human and economic costs:6

To put this into perspective, John Leake writes on Courageous Discourse, "Note that this death count in one year is 5.2 times the number of men killed in 10 years of combat in Vietnam," adding:7

"Perhaps the most extraordinary thing about this state of affairs is that most Americans don't know it's happening. Every day, young people are dying from heart attacks, strokes, and seizures caused by COVID-19 vaccines. Most of their families and friends are led to believe that they just died — suddenly and unexpectedly — of acute conditions that were extremely rare in young people prior to 2021."

The report included data from employed individuals between the ages of 16 and 64, and categorized the impact into four broad groups:

  1. No effect or asymptomatic

  2. Mild to moderate outcome including a temporary or short-term, long-term or permanent injury

  3. Severe outcome that leads to a disability

  4. Extreme outcome leading to death

While group 1 was the largest, comprising an estimated 82% of the population, the authors pointed out that these groups are dynamic, and individuals in one group could move into another, particularly in the case of progressing from no or minor injury to severe injury, such as we've seen with elite athletes suddenly dropping dead on the field:8

"While these groupings characterize different levels of damage from the inoculations, they are not static and could interact with each other. For instance, there might be individuals who had no visible effects after vaccination but nonetheless could still be impacted from the inoculations and could therefore be represented in the sub-group of injured individuals.

In a similar way, individuals with mild injuries from the inoculations could, over time, develop severe injuries to the extent of being disabled, or an extreme outcome such as death. The likely path of outcomes would be from injury to disability to death.

We need to consider, however, that to a lesser extent there could be individuals who suffer extreme outcomes when they had previously only experienced mild injuries until then. We can relate this with the anecdotes of otherwise healthy athletes suffering heart attacks during sports competitions at an alarming rate since the 2021 inoculations."

'The Multiplier Effects Are Massive'

The effects in the report are only what can currently be measured, and are likely to also be fluid. In terms of economic effects, for instance, the report notes that mortuary companies are likely to benefit while life insurers will be harmed, leading to a reallocation of resources.

Meanwhile, in terms of economic costs, milder damage is associated with greater cost, since a larger portion of working age individuals are affected. For instance, those with mild to moderate injury made up a sizeable 18% of the population. According to the report:9

"We make the assumption that the pool of potentially vaccine-injured individuals is about 18% of the population, which is, the rate of related adverse events reported in the Pfizer clinical trial (minus the baseline rate). These injuries will likely manifest a loss of productivity since, as these individuals are likely to have higher absentee rates and, consequently, higher lost worktime rates, than the pre-2019 baseline.

In fact, we performed an analysis of absence rates and lost worktime rates10 in full time workers (using data provided by the BLS). We observed a large increase in absence rates starting in 2020, but accelerating in 2022. Absence rates in 2022 were about 28.6% higher than in 2019, representing a 11 standard deviation variation."

Further, many other economic costs are harder to account for, such as a worker who's still at work but not able to work to their full potential. When these types of scenarios are factored in, the damages could be even more massive. Dowd tweeted:11

"Our economic damage estimates are what we can measure. The knock effects such as lost productivity due to a worker being present but working at say 50%-75% of capacity is missed plus burn out from those picking up slack. Also supply chain delays are not captured etc and etc. The multiplier effects are massive."

Systematic Review Reveals Serious Harms

A preprint systematic review of papers with data on serious adverse events associated with COVID-19 shots again points to significant risks.12 The review was conducted by Maryanne Demasi, Ph.D., a former medical scientist with the University of Adelaide and former reporter for ABC News in Australia and Professor Peter Gøtzsche, a Danish physician-researcher who co-founded the Cochrane Collaboration in 1993.

It included 18 systematic reviews, 14 randomized trials and 34 other studies, noting that "most studies were of poor quality" and additional randomized trials are needed. Still, their review revealed multiple red flags, including:13

  • Adenovirus vector vaccines increased the risk of venous thrombosis and thrombocytopenia

  • mRNA-based shots increased the risk of myocarditis, with a mortality of about 1 to 2 per 200 cases

  • Evidence of serious neurological harms, including Bell's palsy, Guillain-Barré syndrome, myasthenic disorder and stroke, which are likely due to an autoimmune reaction, was found

  • Severe harms, defined as those that prevent daily activities, were underreported in the randomized trials

  • Severe harms were very common in studies of booster doses after a full round of shots and in a study of vaccination of previously infected people

Further, not only have drug regulators and public health authorities been slow to follow up on safety signals showing serious harms from the shots, Demasi notes, but, "Population-wide recommendations for COVID vaccination and boosters ignore the negative benefit to harm balance in low-risk groups such as children and people who have already recovered from covid-19 (natural immunity)."14

Australian Safety Report — 24-Fold Increase in Adverse Events

It's can be difficult to parse out adverse effects from COVID-19 shots and those due to COVID-19 infection. The Western Australia Vaccine Safety Surveillance (WAVSS) 2021 Report, however, shows a unique viewpoint that made this possible. At the time, there was virtually no COVID-19 circulating in the community, yet the area had a 90% vaccination rate among those 12 years and over.15 Umbrella News reported:16

"There are few regions in the world where most of the population was vaccinated before the spread of Covid in the community. Sealed off from the rest of Australia, and the world, for 697 days, WA's closed border earned it the moniker of the 'hermit kingdom'.

State Premier Mark McGowan noted WA's unique role in the global vaccination trial, remarking to a press conference in early 2022, You see, Western Australia is an experiment. We basically have had very few Omicron cases, we have very high vaccination levels, and we have a very compliant population."

So, what happened in an area of the world that had very few COVID-19 cases and very high rates of COVID-19 shots? An "exponential increase" in reports of adverse events following immunization (AEFI), such that it necessitated changes to the vaccine safety surveillance program at the department in order to manage them.17 According to the report:18

"The number of AEFI reported to WAVSS was significantly higher in 2021 than in previous years (10,726 compared with an average of 276 per year for the 2017-2020 period) due to the introduction of the COVID-19 vaccination program."

As Umbrella News reported, the peak of AEFI reports coincided with the rollout of shot mandates, culminating in a rush of hospitalizations that strained area hospitals:19

"In 2021, AEFIs for Covid vaccines were reported at almost 24x the rate of AEFIs for all other vaccines combined … In the latter half of the year, as AEFIs peaked, the media regularly reported that WA hospitals were under strain, despite the lack of Covid cases.

The highest month for AEFI reports was October, the same month that vaccine mandates were announced for most of the workforce, the vaccine eligibility criteria were expanded to people aged 18 and over, and walk-in vaccinations became available."

Other standouts from WA's report include a 35% increase in myocarditis and a 25% increase in pericarditis compared to background rates. "Shockingly," Umbrella News noted, "the risk of pericarditis in the age group in the age group 25 to 29 years old was 53.5 cases per 100,000 doses of Spikevax. It is perhaps unsurprising that chest pain was the fifth most common reported AEFI for COVID vaccines in 2021."20

COVID Shot Efficacy 'Grossly Overestimated'

While the risks of adverse effects have been downplayed, the efficacy of COVID-19 shots has been overstated from the beginning. Writing in the Journal of Evaluation in Clinical Practice, a research team revealed that multiple biases, including background infection rates and cross-overs from unvaccinated to vaccinated in the early days of the campaign, led to an overstatement of COVID-19 shots' effectiveness.21

"We conclude that "real-world" studies using methodologies popular in early 2021 overstate vaccine effectiveness," the study notes.22 Board-certified internist and cardiologist Dr. Peter McCullough explained that from the lack of efficacy alone, the shots should be removed from the market. And the case gets even stronger when you factor in the significant number of related disabilities and deaths:23

"Multiple sources of bias created illusion that vaccines worked as they failed in the real world … claims that the COVID-19 vaccines worked to reduce spread of infection, hospitalization, and death must be rejected.

The burden of proof has not been met and threats to validity have not been overcome. All of the COVID-19 vaccines should be removed from the market and we should begin the investigative phase into how this massive program failed to stop COVID-19."

[MORE]

According to Conservative Underreported CDC Data, Over 35k Deaths Have Been Reported Following COVID Shots, which is More Deaths than all other Vaccines Combined over the Past 30 Years

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From [HERE] Data published today by the Vaccine Adverse Event Reporting System (VAERS) show  1,541,275 adverse events following COVID-19 vaccines were reported between Dec. 14, 2020, and March 31, 2023. This includes 287,651 reports of serious injuries and 35,048 deaths.

Of the 35,048 reported deaths, 21,870 cases are attributed to Pfizer, 9,914 to Moderna, 2,993 to Johnson & Johnson, and 18 to Novavax. Of the reported deaths, 9% occurred within 24 hours of vaccination, and 13% occurred within 48 hours.

VAERS is a voluntary reporting system co-managed by the U.S. Food and Drug Administration and Centers for Disease Control and Prevention (CDC) designed to detect vaccine safety signals.

In the U.S., 673 million COVID-19 vaccine doses had been administered as of March 27, including 401 million doses of Pfizer, 252 million doses of Moderna, 19 million doses of Johnson & Johnson, and 82,000 doses of Novavax.

Bivalent Booster Data

As of April 5, the CDC reported 55.3 million people had received an experimental bivalent booster dose targeting the no-longer-existing Wuhan strain and obsolete BA.4/BA.5 omicron subvariants.

Since the rollout of bivalent boosters in September 2022 and March 31, there have been 27,173 adverse events reported to VAERS, with 40% attributed to Moderna’s booster and 60% attributed to Pfizer/BioNTech. The data included 234 deaths, 2,093 serious injuries, and 80 reports of myocarditis and pericarditis (heart inflammation).

The CDC uses a narrowed case definition of myocarditis. To meet the case definition of myocarditis, people must have had “symptoms such as chest pain, shortness of breath and feelings of having a fast-beating, fluttering or pounding heart, and medical tests to support the diagnosis of myocarditis and rule out other causes.” This allows them to exclude cases of cardiac arrest, ischemic strokes, and deaths due to heart problems that occur before one has the chance to go to the hospital, obtain a diagnosis, or “dies suddenly.”

The CDC website does not state what happens to these cases, but there is no indication they are tracked or included in the CDC’s myocarditis numbers.

Data for 6-month-olds to 5-year-olds

Data for 5- to 11-year-olds

Data for 12- to 17-year-olds

Data for all age groups to VAERS

Although healthcare providers are required by law to report vaccine adverse events to VAERS, research shows very few do. It is essential that anyone who experiences an adverse event report their own injury.

Since the COVID Vax Rollout there has been a Marked Increase in Near Miss Crashes and Medical emergency-related Fight Diversions. CHD asks DOT Secretary Buttigieg to Investigate

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From [HERE] Robert F. Kennedy, Jr. today called on U.S. Secretary of Transportation Pete Buttigieg to investigate the spike in near-misses and narrowly averted airline accidents resulting from pilots incapacitated by health emergencies since 2021, coinciding with the rollout of the COVID-19 vaccination campaign in the U.S.

In a letter to Buttigieg, Kennedy wrote:

“Secretary Buttigieg, the safety of pilots, cabin crew, airline passengers, and the general public is not and never has been a partisan issue. Everything contained within this letter pertains to fundamental issues of public health and safety, which you, the DOT, the FAA, and the Biden Administration profess to uphold and to protect.

The changes to FAA guidelines and the lack of publicly available evidence on which these changes rest, along with the increasing number of incidents involving the incapacitation or vaccine-related injury of pilots, are highly concerning.”

A Children’s Health Defense (CHD) analysis of raw data obtained from the Federal Aviation Administration (FAA) determined there was a marked increase, on a per-flight basis, in medical emergency-related flight diversions in both 2021 and 2022, compared to 2019 and prior years, Kennedy said.

Similarly, there was a marked increase in medical emergency diversions on a per-passenger basis in 2021 compared to 2019 and prior years, while the 2022 figure is higher than those for 2018 and 2019, indicating an increase in medical emergencies occurring in the air, when adjusted for the reduced number of flights and passengers in the 2021 and 2022 calendar years compared to the pre-2020 period.

Kennedy said the FAA violated its own guidelines by recommending COVID-19 vaccines authorized for emergency use for pilots, contrary to the agency’s policy of prohibiting pilots from taking any medical product that has been on the market for less than 12 months.

Kennedy’s 13-page letter citing 69 sources detailed evidence the FAA loosened medical restrictions for conditions such as myocarditis and Guillain-Barré Syndrome, both documented adverse events related to COVID-19 vaccines.

The letter outlines 12 questions Kennedy said Buttigieg and the FAA need to answer for the American public and demands a thorough investigation into whether COVID-19 vaccines may be endangering pilots, flight crews and the public.

‘COVID Shots are a Biological Weapons Project Run by the US Department of Defense,’ according to a fmr Big Pharma Executive

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From [HERE] The U.S. government’s COVID-19 vaccination effort is a biological weapon project run by the U.S. Department of Defense (DOD), according to Alexandra Latypova, a former pharmaceutical research and development executive with 25 years of industry experience.

Latypova, who oversaw compliance for more than 60 clinical trials, knows the regulatory standards pharmaceutical companies historically were required to meet before bringing a product to market.

“People misunderstand that this is just another instance of Big Pharma corruption,” she told Robert F. Kennedy, Jr., chairman and chief litigation counsel for Children’s Health Defense, during an episode of “RFK Jr. The Defender Podcast.” “It’s much, much bigger than that.”

Latypova said we have government reports describing the COVID-19 vaccines as a biological weapon. “I have a question to our government,” she said. “What is it that they’re exactly forcing on us?”

The DOD is “fully in charge” of the COVID-19 vaccine clinical trials and the vaccine’s manufacturing and distribution, and it owns the vaccine “until it is injected into a person,” she said.

By creating a “pseudo-legal structure” over time that included Emergency Use Authorization (EUA) and other transaction authority agreements — called OTAs — the U.S. government allowed the military to take over the distribution of vaccines without adhering to historical safety testing guidelines or product recall procedures.

According to Latypova, the notion that the COVID-19 vaccines met regulatory standards for safety and effectiveness was the “biggest lie that was sold to the public.”

“I am describing a very illegal structure that’s made legal on paper,” she said. “It’s unlawful. They — the government — are driving this.”

Kennedy agreed with Latypova and pointed out that OTA was designed to allow the Pentagon to quickly buy weapons and weapons systems without paying attention to any existing regulatory authorities.

Kennedy said:

“What they’ve done is they’ve taken that authority and they’ve applied it to the vaccines so they’re purchasing the vaccines under OTA as a demonstration product.

“It’s all a huge military operation and the involvement of the drug companies is a kind of window dressing.”

The DOD paid the pharmaceutical companies for their brand names so people would think they were getting something from Pfizer or Moderna — but all of the distribution and manufacturing is done by the military, Kennedy said. The pharmaceutical companies were brought in to put their name on it and then to pretend to do clinical trials, he said.

Latypova and Kennedy discussed how the military accomplished this without most workers involved in the production and distribution of the vaccine catching on.

They also discussed how citizens and lawyers might effectively challenge the Pentagon’s COVID-19 vaccination project in the court system.

Class Action in South Africa says Pfizer’s COVID Injections are Harming and Killing People and Providing No Benefit. Supports Factual Clam that Pfizer Knew from the Beginning Vax was Deadly w/Data

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From [HERE] The Freedom Alliance of South Africa (FASA) filed a show cause action on Monday with the High Court of South Africa. FASA is calling for an urgent judicial review of Pfizer’s mRNA COVID vaccine over concerns the product is harmful. 

The filing includes a real-world data analysis showing an association with increasing death from both COVID and non-COVID causes in the vaccinated compared to the unvaccinated.

The plaintiffs are asking the court to review and rescind Pfizer’s emergency use authorization used to distribute the vaccine immediately. If the case proceeds, it would be the first time Pfizer has had to answer for its vaccine side effects. 

In an interview, cardiologist Dr. Aseem Malhorta said FASA, a grassroots movement made up of supporters, media, doctors, lawyers, and experts brought a case to the high court calling for a judicial review of Pfizer’s products stating the evidence suggests Pfizer’s COVID vaccine is not safe or effective. 

“What that means is that if it is successful, it will result in Pfizer’s product being removed from the market,” Malhotra said.

“What they’ve said is the medical regulator in South Africa did not do its duty — the suggestion is they approved this vaccine on the basis of irrationality, you know because the data that was used to make these decisions were based upon Pfizer’s own data which was commercially conflicted. “

Malhotra continued: 

“They designed the analysis — the suggestion is there was manipulation of the data from real-world evidence because they told us at the beginning it was 95% effective at preventing infection. That very quickly turned out not to be true. That really is what this case is about. “

“It’s also important to emphasize, that, of course, there’s been a real problem getting this discussion and both sides of the story into the mainstream media. That will not be an issue in a court of law. In a court of law, all sides will get an airing, and all sides will be heard,” he added. “When you look at the totality of the evidence its a very different picture from what we were told in the beginning that this was safe and effective. “

Malhotra has been calling for a complete suspension of COVID vaccines because the evidence suggests the harms are considerable and the benefits are negligible. Malholtra’s father died prematurely from an mRNA COVID-19 vaccine injury. 

This case will go forward in the upcoming months and proceedings will be open to the public.

Robert Kennedy’s Class Action Alleges Biden Admin and Feds Colluded with and Pressured Social Media Companies to Suppress Speech About the Dangers of Deadly, Experimental COVID Injections

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From [HERE] On Friday, Robert F. Kennedy, Jr., Children’s Health Defense (CHD) et al., filed a class action lawsuit against President Joe Biden and numerous other federal agents and agencies in the U.S. District Court for the Western District of Louisiana, Monroe Division. The complaint alleges that the defendants have colluded with, encouraged and pressured social media companies to suppress speech that the government does not want the public to hear and to silence specific speakers who are critical of federal policy.

This class action, brought on behalf of all Americans who access the news from social media platforms, seeks nationwide injunctive relief on behalf of those Americans. Instead of seeking monetary damages, the claim asks the court to declare that the Defendants’ conduct violates the First Amendment and to prohibit them from engaging in any form of social media censorship in the future.

The complaint calls the government’s campaign to censor online speech one of “the gravest threats to free speech this country has ever faced.”

“Because of the historically unprecedented power wielded by a handful of behemoth social-media companies over the content of American public discourse, the federal government’s systematic campaign to induce these companies to censor speech is among the gravest threats to free speech this country has ever faced. …

Since 2020, an army of federal officers, at every level of the government—from the White House itself to the FBI, the CIA, the Department of Homeland Security, the CDC, the Office of the Surgeon General, and numerous less-well-known federal entities—has been engaged in the effort to induce those companies to censor constitutionally protected speech.”

“U.S. Supreme Court Justice Potter Stewart said, ‘Censorship reflects a society’s lack of confidence in itself. It is a hallmark of an authoritarian regime.’ It also violates the constitution,” CHD Chairman and Chief Litigation Counsel Robert F. Kennedy, Jr. said. “The collaboration between the White House and health and intelligence agency bureaucrats to silence criticism of presidential policies is an assault on the most fundamental foundation stone of American Democracy.”

“The most serious threat to free speech of our time—and probably one of the most serious in the nation’s history—is the federal government’s massive, concerted and extraordinarily successful effort to get social media companies to censor ideas and information the government doesn’t want people to see, say or hear,” said Jed Rubenfeld, co-counsel for Plaintiffs. “This lawsuit challenges that censorship campaign, and we hope to bring it to an end. The real victim is the public, which is why we’ve brought this suit as a class action on behalf of everyone who accesses news from social media.”

CHD President and General Counsel Mary Holland said, “If Government can censor its critics, there is no atrocity it cannot commit. The public has been deprived of truthful, life-and-death information over the last three years; this lawsuit aims to have government censorship end, as it must, because it is unlawful under our constitution.”

Representing the Plaintiffs in addition to Mr. Rubenfeld is Louisiana Attorney G. Shelly Maturin, II.

New Oral Polio Vaccine Created by The Pathocracy [Bill Gates, WHO] Paralyzing Black Children in the Congo and Burundi

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From [HERE] Experts have long understood that a new polio vaccine developed to try to minimize the risks associated with the oral polio vaccine made by Albert Sabin might also cause the problem it was created to sidestep. It’s now clear that theoretical risk is a real one.

The Global Polio Eradication Initiative announced Thursday that six children in the Democratic Republic of the Congo and one in Burundi have been paralyzed by viruses from the new vaccine, which is referred to as novel oral polio vaccine, or nOPV2. (The “2” signals the vaccine targets type 2 polioviruses.) In addition, five environmental samples collected from Burundi contained the so-called type 2 circulating vaccine-derived polioviruses, or cVDPV2s.

“We are disappointed,” said Ananda Bandyopadhyay, deputy director for technology, research, and analytics on the polio team of the Bill and Melinda Gates Foundation, a partner in the polio eradication effort. “Any such outbreak is disappointing.”

The Gates Foundation is one of a half-dozen partners in the Global Polio Eradication Initiative. The others include the World Health Organization; UNICEF, the United Nations Children’s Fund; the Centers for Disease Control and Prevention; Gavi, the vaccine alliance; and the service club Rotary International. [MORE]

Strict Safety Standards for Cough Syrup, but Deadly mRNA Shots Get a Free Pass

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From [HERE] The Telegraph recently reported that the public have been told to stop taking cough and cold medicines over safety fears concerning the drug, pholcodine, an opioid cough suppressant. 

Twenty of the common cough and cold medicines, including Day and Night Nurse capsules, have been urgently withdrawn from the market on the order of the drug regulators because of concerns about a “very rare” risk of anaphylaxis, a life-threatening adverse event. 

The ‘Class 2 Medicines Recall’ announcement taken from the UK government’s website, is shown below. 

When it comes to the mRNA COVID-19 vaccines, the regulatory double standards have never been so glaringly obvious. 

Anaphylaxis was identified as an important risk by the European Medicines Agency, as early as December 2020, in the EMA’s CHMP (Committee for Medicinal Products for Human Use) assessment report on the Pfizer-BioNTech COVID-19 vaccine, seen below. [MORE]

Genocide Continues: Despite Documented Dangers, No Benefit and No Emergency, USDA Grants Emergency Use for 4th Experimental COVID Shot for Infants and Kids Under 5. No Liability for Injury or Death

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“The federal government has given complete immunity to Pfizer, Moderna, and J&J for any injury caused by their Covid-19 vaccines.  That’s right: you cannot sue them if you are injured by their Covid-19 vaccine.  (See Note 1 to read the law yourself.)  So, while their product may not give you immunity, Pfizer and Moderna are guaranteed immunity.  Said immunity also shields doctors, hospitals and any other persons who administer or coerce people to take deadly COVID injections.

And it gets even worse.  These companies are even immune for – hold your breath – willful misconduct.  That may sound crazy, but it is shockingly true.  You can only sue them for willful misconduct if the federal government first sues them for such conduct.  (See Note 2 below to read the law yourself.)  And what are the odds the federal government will do so after wildly promoting the vaccine?  About as likely as the FDA ever admitting they promoted a vaccine that caused widespread harm.” [MORE]

From [HERE] Infants and children 6 months through age 4 who received the three-dose primary series of the Pfizer-BioNTech COVID-19 vaccine are now eligible for a fourth dose — Pfizer’s bivalent booster shot.

The U.S. Food and Drug Administration (FDA) on Tuesday amended the Emergency Use Authorization (EUA) of Pfizer bivalent COVID-19 booster vaccine for the younger age group, but only for those children who received the three-dose series before the FDA authorized Pfizer’s bivalent Omicron booster as the third shot in the primary series.

Under the amended authorization, children can receive their fourth shot two months after completing the three-dose primary series.

Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research, said the authorization gave parents the opportunity to “update their children’s protection.”

But critics including Peter McCullough, M.D., MPH, an internist and cardiologist, said the shots pose long-term safety concerns for children.

“I am greatly concerned about the long-term safety of accumulating novel mRNA and Wuhan spike protein in previously healthy children,” McCullough told The Defender. “Continued shots are not natural and cannot make their bodies healthier.”

Mary Holland, president and general counsel of Children’s Health Defense said:

“If one ever needed proof of which side the FDA is on, Pharma’s or the people’s, one need look no further than its authorization of a fourth COVID shot for children under 5.

“With knowledge that these shots don’t work and that they can cause severe harm, including death, this decision is simply obscene.”

Dr. Michelle Perro, a pediatrician with more than 40 years of experience in acute and integrative medicine, told The Defender, “Medical logic and reason have taken a back seat to an unfathomable policy based on fiction.”

Perro added:

“With the steady stream of information now available on VAERS [Vaccine Adverse Event Reporting System] and other global vaccine reporting systems, the harm caused to children from this unnecessary ‘vaccine’ is nothing short of pediacide.”

Perro pointed out that according to some researchers’ estimates, children under 18 are 51 times more likely to die from the mRNA vaccines than from COVID-19 if unvaccinated.

Perro, who said she will deliver a conference lecture in April on how to help children who have been harmed by the COVID-19 vaccines, said:

“The time is now for parents to do what’s best for their children and refuse this experimental technology.”

New clinical trial had ‘no published results’

The agency said it based its decision to authorize the fourth shot on previous analyses of earlier Pfizer COVID-19 vaccine efficacy data and on new clinical trial data from 60 children ages 6 months through 4 who, after completing the three-dose primary vaccination and receiving the booster shot, “demonstrated an immune response” to both the original COVID-19 virus strain and the Omicron subvariants.

The new clinical trial “had no published results” but was presented to the FDA in a Jan. 26 meeting slide show, said blogger Igor Chudov.

According to Chudov’s analysis, the data included “the strangest count of participants.”

Slide 16 of the presentation showed there were 21 babies in the clinical trial before the fourth shot — and 23 babies after the shot, he pointed out.

“How is that even possible? And why did no one present at the FDA meeting ask questions?” Chudov asked.

Chudov pointed out that under the new authorization, the four-dose vaccination sequence could be completed within four months after starting at age 6 months.

“Therefore, a 10-month-old infant could have four mRNA Covid vaccine doses,” he said.

Dr. Meryl Nass, an internist and epidemiologist and member of the Children’s Health Defensescientific advisory committee, said the official data released by the U.K. and German governments suggest you are 20 times as likely to injure a child with an mRNA vaccine than to benefit them.

In a Substack post today, Nass said Dr. Scott Jensen, a family physician and former Minnesota State Senator, noted that the number of mRNA vaccine doses needed to vaccinate young children to prevent one hospitalization for severe illness is more than 224,000 doses.

Assuming the risk of injury due to the COVID-19 vaccine is similar for children to the overall risk the German health minister disclosed, you would have to vaccinate more than 112,000 5- to 11-year-old children with two shots and seriously injure 22 of them as a result, in order to prevent one COVID-19 hospitalization.

“Anyone who is cognizant of these data and recommends mRNA COVID vaccines for children is in my view guilty of professional malfeasance, a crime and needs to immediately be brought to justice,” said Nass.

Fauci Caught Going to Door to Door Lying to Black People About COVID Shots: Consent to Medical Experiments Obtained by Inducement, Coercion, HalfTruths, Nondisclosures, etc is Fraud, Battery or Murder

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A newly surfaced 2021 video of Dr. Anthony Fauci going door to door with an entourage that included SNigger Muriel Bowser, the Mayor of DC has gone viral two years later. Bowser, a black rolebot in service of elite white liberals, functions as his “jungle guide” through the black neighborhood. The video shows Fauci making various misrepresentations, lies, omissions and half-truths in attempt to induce Black residents to take deadly COVID mRNA shots. Said experimental injections have no benefit and are harming and killing people globally in a slow motion extermination of humanity. In the short video most residents appear to pass the “IQ test” - that is, they reject Fauci and his rolebotic companion’s deceitful invitation to take genocidal COVID shots. Nevertheless, untold millions have been induced, coerced or tricked into taking said injections, thereby destroying their individual physical and mental integrity. [MORE]

According to FUNKTIONARY:

biocide – the attempted annihilation of all life, which is the intent of Doggy and CrimethInc. (See: Doggy & CrimethInc.)

genocide – the intentional decreasing of the people of a given population or asili, particularly in the interests of another population or value-system that wishes to control the resources of the victims. 2) the-cide-show of the World Health  Organization (WHO). Blindness to economic reality has placed mankind in a very precarious position. Our freedom and very lives depend on how (and how soon) we resolve resource misapplication and inequalities. (See: Population Control)

Family Members say Colorado HS Football Standout Markus Martinez's Massive Heart Failure Was Triggered by COVID Injections. Formerly Fit, Healthy and Strong Athlete Now Needs Heart Transplant

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From [HERE] A local high school football star in the Denver area went from a fully healthy 17-year-old to near death due to massive heart failure with no apparent preexisting conditions that would indicate such an event even plausible. However, one intervention that did occur that no mainstream media is talking about is COVID-19 vaccination. According to Markus Martinez’s great aunt Valerie Pacheco, Markus received the jab before the incident and that is most certainly, in her opinion, the cause of this near-death experience. Now 18 years of age, Markus had to get a heart transplant in January 2023, and by February was back in Aurora Colorado hospitals for the dangers associated with blood clots. How does that happen—a totally fit, strong, award winning high school athlete goes from absolute health to the need for a new heart and massive blood clots? If great aunt Valerie Pacheco is correct, it all can be explained by the COVID-19 vaccination that occurred prior to Markus’ cardiovascular-based health crisis. Afterall, Markus fits into a category of known risk cohorts—young men with a higher probability for myocarditis, a cardiovascular condition.

Markus Martinez

The former Columbine High School football star has been in and out of hospitals as doctors earlier this year declared he would need a heart transplant—he received one during January of this year. The heart failure occurred during November of 2022.

TrialSite spoke with Markus Martinez’s great aunt, Ms. Valerie Pacheco to learn more about the incident after a review of local news coverage earlier in the year from local affiliate Fox31 Denver (KDVR).

Reporting for the local affiliate, Samantha Spitz spoke with both parents including Shelly Segura and Steven Martinez. According to his mother, his heart only functions now at 12% to 15%, meaning they realized at the time that her son would need a new heart as soon as possible. Segura was quoted, “His heart is just unfortunately too sick right now.” She continued, “We’ve all come together and have been praying for him. We’re really trying to stay positive for Markus.”

Martinez’s went on the record for the Denver area Fox News affiliate, “It’s been a little tough on him that he can’t get up, get out of bed and do his normal activities and stuff that he used to do, but he’s hanging in there.”

Markus’ brother Steven Martinez was approached by the Fox affiliate as well, stating, “I just couldn’t believe it was happening to someone so young and athletic.”

The Heart Transplant

The good news earlier this year, UTHealth University of Colorado Hospital in Aurora, was able to perform a successful heart transplant on January 26, 2023, according to his GoFundMe site.

With initially a successful procedure, conditions again worsened further burdening Markus’ health. Since the heart transplant less than two months ago Markus has been in and out of the hospital. While home in early February last month he started feeling severe pain in his chest, back, and legs.

His family took him back to the hospital where it became apparent the young man presented three blood clots, one in each lung and one in his right groin area. As reported on his Go-FundMe page, the blood clot in his right groin impacts the blood flow to the lower leg region, resulting in another surgery.

Not surprisingly, the healthcare costs have mounted, and the family faces severe financial difficulty due to the ongoing treatment.

What about the Vaccine Connection?

Not surprisingly, the Fox affiliate remained quiet about the fact that Markus not only received the COVID-19 vaccine, but that he was in the cohort of young men facing higher risk for cardiovascular safety incidents such as myocarditis. See the FDA label for the Pfizer vaccine as an example. According to the package insert:

“Postmarketing data demonstrate increased risks of myocarditis and pericarditis, particularly within 7 days following the second dose.”  

Valerie Pacheco, Markus’ great aunt, spoke with TrialSite, sharing that the severe, dangerous cardiovascular event directly links to the COVID-19 vaccine administration.

Valerie said that it took a while for the family to internalize what is a truly painful reality: that this seemingly vaccine-induced severe injury has been avoided totally by all health providers involved. According to Ms. Pacheco, health providers won’t even discuss the potential of a COVID-19 vaccine injury despite the fact that the incident occurred after vaccination. TrialSite is probing to determine actual proximity. The incident has not been reported to the Centers for Disease Control and Prevention Vaccine Adverse Events Reporting System, according to great aunt Pacheco.

TrialSite has reached out to Markus’ mother Ms. Segura for further discussion and will update this article should she want to come forward. TrialSite cannot be certain that this massive cardiovascular failure was caused by the vaccine, but this is certainly what family members believe.