Tag: vaccines

Bill Gates unleashes plan for new series of gene-based injections that will target Africa

Microsoft co-founder Bill Gates is rolling out a plan to use Africans as guinea pigs for an expanded series of new genetically altering mRNA injections.

He calls them vaccines but we know they are not vaccines, at least not in the traditional meaning of the word. U.S. courts have even ruled that mRNA serums don’t qualify as vaccines.

The Covid vaccines, the first to use this technology, have been an unmitigated disaster.

But that hasn’t stopped Gates from pushing more of these gene-based jabs on the world.

The Bill & Melinda Gates Foundation has announced a $40 million initiative to support the production of messenger mRNA vaccines in Africa.

Gates’ foundation claims this investment will address what it refers to as “vaccine inequities” exposed during the COVID-19 pandemic.

During that pandemic, African nations were often the last to receive Covid jabs. It worked to their benefit as fewer Africans died of Covid, per capita than Westerners.

Yet, the power of money never ceases and so Gates presses on in his efforts to vaccinate the world against every disease imaginable. And Africa will be ground zero for the plan.

Gates and his foundation hope to expand the testing of the mRNA injections on Africans before they are rolled out globally.

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A Young Child Died During Moderna Covid Vaccine Clinical Trial — Did FDA Know?

A preschool-aged child died of cardio-respiratory arrest after getting a COVID-19 booster in a Moderna clinical trial. However, Moderna didn’t reveal the death to the public and only recently reported it on a European regulatory agency database, Alex Berenson reported.

The death occurred in late 2022 or early 2023, Berenson said, when children under 5 who had already received Moderna’s original mRNA-1273 COVID-19 vaccine in the trial’s main phase were offered the “1273.214” booster against an early Omicron variant.

Berenson, a former New York Times reporter who now reports on his Unreported Truths Substack, today said the U.S. Food and Drug Administration (FDA) has declined to tell him whether the U.S. agency knew that a child died during Moderna’s clinical trial.

The failure of the FDA to provide a straightforward answer about whether it knew that a young child in a Moderna clinical trial died from cardiac-respiratory arrest is “vitally important,” Berenson told The Defender.

“Of all the mistakes public health authorities made around COVID, their insistence on pressing mRNA vaccines on children was probably the worst,” Berenson said.

By the time the COVID-19 vaccines were available for kids, it was clear that children were at almost no risk of serious illness or death from COVID-19, he said. “The shots had significant side effects, so the only rationale for giving them shots — even theoretically — was to reduce transmission.”

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Drones Spray ‘Self-Spreading’ COVID-19 Vaccine for ‘Large-Area Inoculation of Humans’ in ‘DEFUSE’ EcoHealth/DARPA Project

  • EcoHealth’s DEFUSE Proposal Exposed: In 2018, EcoHealth Alliance submitted a proposal to DARPA, codenamed DEFUSE, outlining plans to deploy aerosolized immune modulators, chimeric spike proteins, and/or self-spreading vaccines via drones, potentially over humans.
  • Aerosolized Vaccination on Humans: DEFUSE documents explicitly describe large-area aerosol delivery systems for “inoculation of animals/humans,” raising the question of whether these plans were executed on unsuspecting populations.
  • Drone Deployment and Pandemic Origin: The DEFUSE proposal and DARPA’s advanced drone programs suggest a chilling possibility: that drones may have played a role in the COVID-19 pandemic, challenging the mainstream lab-leak narrative.
  • DARPA’s Connection to Moderna: By 2012, DARPA was already working with Moderna on RNA-based spike protein vaccines. A 2016 Moderna patent contains a genetic sequence with a one-in-3-trillion match to the pandemic virus, igniting claims of bioengineering origins.
  • Suppression of DEFUSE Details: Whistleblower revelations show attempts by DARPA and intelligence agencies to classify and censor DEFUSE-related research. U.S. senators have demanded investigations into these actions.
  • Self-Spreading Vaccines and Gain-of-Function: DEFUSE documents reveal plans for self-disseminating vaccines and host-to-host therapeutic distribution, indicating the potential use of engineered viruses as vaccine delivery systems.
  • Unprecedented Drone Funding Surge: A 26% spike in military drone funding in 2019 aligns with DEFUSE’s timeline and its drone-based aerosol delivery technologies, hinting at pre-pandemic preparations.
  • International Drone Use During COVID-19: Governments worldwide deployed drones for “disinfecting,” but studies debunk the effectiveness of this practice, raising suspicion about the true purpose of these operations.
  • A Coordinated Bioengineering Agenda?: The alignment of DEFUSE, DARPA, and drone advancements reveals an unsettling intersection of gain-of-function research, bioweaponized delivery systems, and self-spreading vaccines.
  • Urgent Transparency Needed: The DEFUSE project raises alarming questions about the origins of COVID-19, the ethics of aerosolized bioengineering, and the U.S. government’s role in these developments. The public deserves truth and accountability, especially considering a potentially incoming bird flu pandemic.

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More Big Pharma/Big Government Attacks Coming – Arepanrix: Package Insert & Approval Letter

By now, readers know this writer is a staunch advocate for proper informed consent following the informed consent process. Previously, the injectable vaccine AUDENZ for H5N1 manufactured by Seqirus was reviewed to inform the public about the product. While it was a long read, the package insert for AUDENZ proved there were not enough participants to represent the population, placebo-controlled trials were only conducted in one study, and the one-year follow-up was not long enough to uncover potential serious adverse events relating to development of autoimmune diseases. Understandably, reading package inserts is not particularly “attention-grabbing” and can be quite boring and tedious. However, it is the only way you will receive all the information you need to give proper informed consent, which includes denying taking a product. Because of the volume of data to be covered in the AREPANRIS package insert, it will be covered in two parts.

In this article, the approval letter and package insert for AREPANRIX will be reviewed. The only approval letter for AREPANRIX on the Food and Drug Administration (FDA) website is dated October 18, 2024. This letter references another letter dated April 19, 2024, which requested a supplement to their license regarding packaging to include the proprietary name of AREPANRIX. There should be another letter indicating the initial FDA approval for this vaccine. Without the initial approval letter, there is no additional information to be gleaned besides the package insert.

AREPANRIX, manufactured by GlaxoSmithKline (GSK), is approved for active immunization for the prevention of disease caused by the Influenza A virus H5N1 subtype contained the vaccine for individuals 6 months and older. AREPANRIX comes in two vials that must be mixed before administration: one contains the H5N1 antigen and the other contains the AS03 adjuvant. The AS03 adjuvant will be explained in Part II. For individuals ages 6 months through 17 years, two doses of 0.25 ml are injected intramuscularly 21 days apart. For individuals ages 18 years and older, two doses of 0.5 ml are injected intramuscularly 21 days apart. (Sections 1 through 2.2)

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COVID Vaxx Team Trialing Bubonic Plague Vaccine as Fears of Next Pandemic Grow

British scientists who worked on the Astrazeneca COVID-19 jab are calling for the UK to stockpile vaccines for the bubonic plague, as fears about the next global pandemic grow.

Britain’s Daily Telegraph reports that scientists with the Oxford Vaccine Group are worried the UK could be caught unprepared by a global pandemic of the disease which killed tens of millions of people the Middle Ages.

The Oxford Vaccine Group has been trialling a plague vaccine since 2021, on a group of 40 healthy adults. The group’s leader, Professor Sir Andrew Pollard, says the vaccine has proven a success, and results of the trial will be submitted to a scientific journal for peer review within weeks. Further clinical trials are expected.

Pollard said: “There are no licensed plague vaccines in the UK. Antibiotics are the only treatment. There are some licensed vaccines in Russia.

“The risk in the UK is currently very low. Previous historical pandemics that had high mortality were associated with initiation from fleas on rodents but were driven by person to person spread.”

Military scientists in the UK believe the plague, which still exists in isolated pockets around the world, has the “potential for pandemic spread.” Scientists from the UK government’s biological research facility at Porton Down recently wrote a paper claiming that vaccine production needs to be enhanced “to prevent future disastrous plague outbreaks.”

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Song About Fauci and Genocide Gets COVID-19 Doctor Turned Musician Cancelled

An Australian medical doctor who worked on the front lines of the COVID-19 pandemeic, who later turned to become a rising musician, Iyah May, recently released the 2024 political version of Billy Joel’s 1989, “We Didn’t Start the Fire,” entitled Karmaggedon. She was fired by her manager and record label for not changing the lyrics of her controversial song which accurately and truthfully depict today’s state of society.

Per the Iyah May’s website, “The song doesn’t shy away from addressing the pandemic narrative, corruption within political, pharmaceutical, and health institutions, the Israel-Palestine conflict, violence against women and the social chaos that has swept through the world in the past few years.”

“Fuelled by my own despair over a divided world and deceitful corporations, I channelled my frustration into Karmageddon. My career as a doctor has been greatly impacted, and I was affected on a deep and personal level,” states Iyah May.

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FDA’s Own Study Finds DNA Contamination in Pfizer Vaccines

A peer-reviewed study performed at a U.S. Food and Drug Administration (FDA) laboratory by high school students has confirmed the presence of a high level of DNA contamination in Pfizer’s mRNA COVID-19 vaccine.

The study, published Dec. 29, 2024, in the Journal of High School Science, was authored by three students at Centreville High School in Clifton, Virginia, and performed under the supervision of FDA scientists.

Maryanne Demasi, Ph.D., an investigative medical reporter, was the first to report on the study.

The research, performed at the FDA’s White Oak Campus in Maryland, found that levels of residual DNA in the Pfizer COVID-19 vaccine were 6 to 470 times higher than regulatory safety limits. The students tested two lots of the vaccine, finding they contained “residual DNA to a level that exceeds 10 ng [nanograms] per dose.”

“The potential health risk posed by residual small DNA fragments is currently unknown,” the study stated. However, the authors also said that DNA contamination may result in insertional mutagenesis — or DNA mutations — that can cause cancer.

Speaking last month on “The Defender In-Depth,” Kevin McKernan, who first identified DNA contamination in the shots in 2023, said DNA in vaccines can pose health risks because the DNA “could integrate into the genome and cause disruption of the genome … or it could disrupt other genes that are related to cancer.”

The FDA did not respond to multiple requests for comment on the study.

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British doctor has medical license revoked over warning of COVID shot dangers

British doctors continue to be removed from medical practice for warning patients of the dangers of the so-called mRNA COVID “vaccines.”

In December 2024, consultant psychiatrist Dr. Daniel Armstrong was struck off the medical register following his description of pharmaceutical companies as “evil.”

Armstrong had appeared in a video shared on BitChute in which he described the COVID regime and the attendant “vaccines” as part of a “deception on a grand scale” – saying the injections put people’s lives at risk. In the video, titled Navigating the Truth-Deception Duality, he said:

My message is clear to everyone: don’t take any more. You’ve a doctor here, he’s got his licence on the line – given it up. Don’t take any more of the injections. These guys are evil.

The tribunal which deprived Armstrong of his right to practice medicine concluded he was “highly likely in future to act so as to put patients at unwarranted risk of harm” – as the Daily Mail reported on January 2.

According to the minutes of the tribunal, an anonymous email alerted the General Medical Council to Armstrong’s video – which had been initially released on July 17, 2023.

The tribunal has found that Armstrong’s use of his medical credentials to warn the public of the dangers of the so-called vaccines is a violation of medical ethics, stating the physician had “undermined public health information and posed a serious risk to members of the public who may have placed reliance on his opinions.”

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Covid Vaccines Contain Cancer Virus Fragments & Mutagenic DNA Contamination — Study

A peer-reviewed study published Sunday documented findings from Covid gene-therapy vaccine analysis conducted in the BSL-1 research facility at the FDA White Oak campus. The findings detailed how the mRNA injections contain fragments of SV40 cancer virus, as well as DNA contamination.

“Using 4 vials of experimental mRNA vaccines, we found that two out of four vials of those experimental mRNA vaccines contained residual plasmid DNA that transformed Escherichia coli cells. We subsequently applied our method to assess 2 separate lots of Pfizer COVID-19 mRNA vaccines and found no replication-competent plasmid DNA. However, these authorized vaccines do contain residual DNA to a level that exceeds 10 ng per dose,” the study said in the ‘Abstract’ section.

While SV40 cancer virus fragments were detected, the researchers stated that since it was just fragments it’s unlikely they’d have the same carcinogenic effect as fully intact SV40 cancer viruses, yet may still cause localized reactions.

It should be noted however that other researchers have detected larger SV40 cancer virus fragments in their mRNA Covid vaccine samples.

“Although some investigators have reported the presence of larger DNA fragments with SV40 promoter/enhancer from the commercial mRNA vaccines (18), our results showed the efficient digestion of plasmid DNA in Pfizer COVID-19 mRNA vaccines,” the study said in the ‘Discussion’ section. “Since we only detected DNA fragments < 35 bp in our study, it is practically unlikely for these broken pieces of SV40 promoters to be functional. The plasmid DNA template does not contain oncogenes. Therefore, it is less likely that these DNA fragments will be oncogenic or infectious. Smaller DNA fragments can be immunostimulatory, contributing to local reactions after vaccination.”

Perhaps ironically, the impetus of this study was to “report a simple method to detect residual replication-competent plasmid DNA that is present in mRNA vaccines as impurities” in order to “suggest that stringent and transparent monitoring of DNA impurity may aid in the buildup of public trust in mRNA vaccines.”

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Vermont Supreme Court Ruling Allows Schools to Administer COVID Vaccines Without Parents’ Consent

Numerous mainstream media outlets are deliberately lying to American parents about the law regarding COVID-19 vaccines.

In August, Vermont’s Supreme Court that ruled a 6-year-old boy administered a COVID-19 vaccine against his parents’ specific instructions that he not be jabbed has no state tort remedies, and that the family’s sole recourse is a federal claim requiring proof of serious bodily harm or death to proceed.

All other traditional causes of action for violating these parents’ rights, and fundamental constitutional informed consent protections for patients, are extinguished completely. And yet, numerous media outlets reported the precise opposite. This is blatant misinformation.

The Associated Press (AP) launched an utter deception titled falsely: “Fact Focus: Vermont ruling does not say schools can vaccinate children without parental consent.” This is the opposite of the truth: Politella v. Windham Southeast School District, et al. held exactly that:

“Other state courts faced with similar facts have concluded that state-law claims against immunized defendants cannot proceed in state court in light of the PREP Act’s immunity and preemption provisions, including claims based on the failure to secure parental consent.”

In support of its abject lie, the AP cited a Vermont Law School professor:

“Rod Smolla, president of the Vermont Law and Graduate School and an expert on constitutional law, told The Associated Press that the ruling ‘merely holds that the federal statute at issue, the PREP Act, preempts state lawsuits in cases in which officials mistakenly administer a vaccination without consent.’

“‘Nothing in the Vermont Supreme Court opinion states that school officials can vaccinate a child against the instructions of the parent,’ he wrote in an email.”

Professor Smolla is an embarrassment to the Vermont Law School of which he is President. Politella specifically holds that all state tort claims, including those alleging willful jabbing, are preempted by federal law.

In observable fact, the court ruled that the Politella family could not proceed with their case — even though the complaint alleges that the school “vaccinated a child against the instructions of the parent.” Where did professor Smolla not learn the law? — a 6-year-old can read the case and see the falsehood of his statement.

The Politella court specifically determined that “each defendant is immune from plaintiffs’ state-law claims, all of which are causally related to the administration of the vaccine to [the minor child] L.P.”

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