Intended Consequences: mRNA Vaccines were Designed to Cause Severe Disease and Be Resistant to Antibodies

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Data published by spike protein inventors, Barney Graham & Jason McLellan, COVID-19 mRNA vaccines were purposefully designed to not protect against SARS-CoV-2 or variants and cause disease

by Karen Kingston

Barney Graham of the NIAID and Jason McClellan of the University of Texas are the inventors of the S-2P spike proteins produced by the COVID-19 mRNA vaccines.

In a February 19, 2020 article in Science, authored by the inventors of coronavirus S-2P spike proteins, Barney Graham and Jason McClellan, the authors state that the S-2P ‘spike protein’ has stronger binding affinity to the ACE-2 receptors (in the hearts, lungs, kidneys, and endothelial cell line of blood vessels) than the original SARS-CoV-2 (S) spike protein.

Graham and McLellan also tested synthetically recreated antibodies for coronaviruses (SARS-CoV-2) against the S-2P spike proteins. Their research showed that none of the antibodies for coronaviruses bound to the new trimeric two-proline spike (S-2P) proteins and no coronavirus antibodies were able to neutralize it.

This scientific evidence (authored by the inventors of the spike proteins) confirms that the COVID-19 mRNA vaccines;

  • do not produce antibodies to SARS-CoV-2, and
  • are resistant to the antibodies for SARS-CoV-2, and therefore –

It is scientifically and clinically IMPOSSIBLE for Pfizer’s FDA-approved mRNA vaccines TO PROVIDE ANY PROTECTION AGAINST SARS-CoV-2 infection, or any coronavirus, including ‘VARIANTS’.

The strong binding of the S-2P spike proteins to the ACE-2 receptors (produced by the mRNA vaccines), is further scientific proof that the COVID-19 mRNA vaccines were designed to cause disease. (The S-2P two-proline trimeric spike is different than the (S) wild-type spike produced by the SARS-CoV-2 virus).

Perhaps one can logically conclude that the FDA authorized and approved Pfizer’s mRNA vaccines because the mRNA injections elicited a ‘robust immune response.’ But the FDA had no evidence that the ‘robust immune response’ provides any clinical benefit in reducing the risk of SAR-CoV-2 infection, severe disease, hospitalization, or death. But don’t take my word for it, take the FDA’s.

During the FDA’s December 11, 2020, emergency use authorization meeting for the Pfizer COVID-19 mRNA vaccines, FDA committee members pointed out that the mRNA vaccines appear to provide no clinical benefit, specifically regarding the severe disease.

“Some committee members raised concerns about the small number of severe COVID-19 cases and limited conclusions about the prevention of severe disease based on the study endpoints. FDA pointed out that vaccine development has a long history and that FDA is not aware of an example of any vaccine that is effective against a mild disease that is not also effective against severe disease and that even though limited, data for Pfizer-BioNTech COVID-19 Vaccine suggest efficacy against severe disease.” – FDA EUA Review Committee for Pfizer EUA COVID-19 mRNA vaccines, Dec 11, 2020

Per the FDA’s own words, in the history of the FDA, the FDA has never approved a vaccine that does not protect against severe disease (until the agency approved the COVID-19 mRNA vaccines).

This is where it gets interesting though (and by interesting, I mean ‘evidence of criminal intent’ interesting). Per the data discussed during that same FDA meeting, not only do Pfizer’s COVID-19 mRNA vaccines NOT prevent severe diseasePfizer’s mRNA vaccines cause SEVERE COVID-19 within 7 days of being injected.

Page 41 of PFIZER’s EUA submission, states that there were 409 patients who had COVID-19 symptoms within 7 days of getting their first (1st) or second (2nd) PFIZER shot, BUT these patients did not have a positive PCR test for SARS-CoV-2.

Per PFIZER’s own document, “unconfirmed COVID-19 cases could have masked clinically significant adverse events that would have otherwise been detected.”

Per PFIZER’s EUA submission, clinically significant or severe COVID-19 cases were defined in the Phase 3 Study as kidney, liver, or neurological dysfunction*, low oxygen levels, respiratory failure, mechanical ventilation, systemic shock, admission to the intensive care unit (ICU), or death.

Pages 15-16 of PFIZER’s EUA submission, state that the incidence of expected serious adverse events (reactogenicity) in 100 children aged 12-15 years, was so incriminating that Pfizer and the FDA agreed to not release (cover-up) the data.

Reactogenicity data (including severe adverse events from the October 22, 2020 FDA/Industry meeting) from a total of 100 adolescents 12 through 15 years of age…were provided in the EUA submission. However, the Sponsor (Pfizer) did not request the inclusion of this age group in the EUA because the available data…were insufficient to support favorable a benefit-risk determination at this time. Therefore, the reactogenicity data for participants (children) 12 through 15 years of age are not presented in this document.” – FDA EUA Review Committee for Pfizer EUA COVID-19 mRNA Vaccines, 12/11/20

The FDA knew Pfizer’s mRNA vaccines would permanently injure and harm children. Immediately after this meeting, the FDA should have stopped all trials, especially the trial for children. Allowing the pediatric trials to move forward was a criminal act by the FDA resulting in the unnecessary battery (bodily injury) of children.

Maddie de Garay was a healthy, happy 12-year old girl prior to being a study participant in Pfizer’s 12-15 year old Phase 3 trial. Within 24 hours of receiving her 2nd mRNA Pfizer vaccine, Maddie suffered severe crippling nerve pain, memory loss, vision disturbances, and irregular menstrual cycles. Maddie is suffers particle paralysis and requires a wheel chair and NG tube. Her serious adverse events were recorded as a stomach ache in the Pfizer trial.

During the December 11, 2020, FDA meeting, data was disclosed of a teenager from the 16-17-year-old group (n=77) who was vaccinated with the Pfizer mRNA vaccine. The vaccinated teenager fractured his facial bone structures, likely from the fainting caused by the mRNA vaccines.

Per the September 17, 2021, FDA committee meeting, the FDA has full knowledge that two (2) injections of Pfizer’s mRNA vaccines increase a person’s risk for developing COVID-19 over time versus a person who remains unvaccinated.

In other words, Pfizer’s COVID-19 mRNA vaccines cause COVID-19.

So there you have it. The FDA authorized and approved the COVID-19 mRNA vaccines knowing the injections would cause injury, disease, disabilities, and death at a higher rate than the ‘SARS-CoV-2 virus’ (much, much higher rate).

The FDA mRNA vaccine committee is also well-versed in the immunogenicity and lethality of ‘mRNA vaccines’ based on over a decade of analysis by the agency on protein-based therapies.

Lastly, on October 22, 2020, (prior to any mRNA vaccine authorizations) the FDA had a meeting with the industry, where a list of the expected severe diseases and outcomes caused by the mRNA vaccines was disclosed. When the FDA authorized and then approved the COVID-19 mRNA vaccines, the agency knew that the mRNA vaccines do not prevent severe diseasebut rather cause severe disease and death.

The above list of diseases and outcomes are not side effects. The above list of diseases and outcomes, including death, are the INTENDED CONSEQUENCES of the COVID-19 mRNA vaccines.

Based on the body of evidence submitted to the FDA by Pfizer, the FDA is fully knowledgeable that Pfizer’s COVID-19 mRNA vaccines cause mild-moderate disease, severe disease, injuries, disabilities, and even death in adults and children. The FDA is fully aware that the mRNA vaccines put American adults and children at significant risk for hospitalizations and death while the ‘SARS-CoV-2 virus’ does not.

The evidence in this article is primarily from Pfizer’s documents submitted to the FDA. The other evidence is from the FDA and a peer-reviewed journal authored by the inventors of the 2-SP spike protein produced by COVID-19 mRNA vaccines. Each statement made can be verified with the link provided to a government website (either or where you will find the documents that are cited.

This article is based on evidence that can stand up in a court of law. Please share with local and national government officials, school boards, churches, and your health care providers. Please share with your friends and family. Our loved ones, our communities, and our country can not be healed if they are unaware of how they have been harmed.

The FDA’s approval of COVID-19 mRNA vaccines is not only fraudulent, but it is also a conspiracy to commit premeditated battery and murder of Americans.

The Kingston Report. TRUTH WINS.

Psalm 140: 1-3

“Rescue me, Lord, from evildoers; protect me from the violent who devise evil plans in their hearts and stir up war every day. They make their tongues as sharp as a serpent’s; the poison of vipers is on their lips.”

Take Down COVID-19

The uncomfortable truth is that we all have been lied to and deeply betrayed by leaders we trust, and some we even adored. All offices of power across our nation; from our President and Federal Healthcare agencies to our local governors, mayors, city council members, and even our healthcare service providers, employers, and school board members. If you’re questioning how to know if a government, public official or even if your employer or school is an ally of the American people or our children, there is a simple challenge to give them;

Demand Local Officials Take Down COVID-19.

Call for governors, mayors, school boards, colleges and universities, health care officials, health care centers, businesses, and churches too;

  • Make a public declaration that COVID-19 mRNA vaccines cause disease and death and must be banned and recalled immediately
  • Immediately STOP ALL COVID-19 testing, treatments and mRNA vaccines
  • REJECT and STOP ALL FUNDING for all COVID-19 programs
  • *CALL FOR GOVERNORS to CRIMINALIZE the promotion and administration of mRNA VACCINES

*Governors have the power to reject the HHS declaration that SARS-CoV-2 is a threat to public health and national security and to criminalize the use of all EUA-designated COVID-19 products, tests, and mRNA vaccines. Demand that they do.