Tuesday, November 29th, 2022

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Operation Warp Speed unleashed a new era of science fraud – untested mRNA jabs now fast-tracked for RSV, flu, heart disease and endless covid variants

Operation Warp Speed unleashed a new era of science fraud – untested mRNA jabs now fast-tracked for RSV, flu, heart disease and endless covid variants

(Natural News) Operation Warp Speed (OWS) would go on to unleash a new era of science fraud and medical tyranny. The initial mRNA jabs did not stop “covid-19” and only added new health problems and caused further suffering and death to the general population. Since OWS, “science” has fast-tracked mRNA jabs for RSV, flu, heart disease and endless covid variants.

Predatory vaccine development has destroyed scientific integrity and made a mockery of the scientific method, poisoning the population for profit. The covid-19 vaccine was in the works long before a causative agent was ever identified for the “global pandemic.” A confidential agreement between Moderna and the NIAID (dated December 12, 2019) authorized a transfer of “mRNA coronavirus vaccine candidates” to recipients at the University of North Carolina. It had been eight years since a coronavirus posed a threat to humans, yet Moderna, with investments from the Bill and Melinda Gates Foundation, was ready with a “vaccine” before the causative agent was identified in January 2020, before a pandemic was ever quantified.

Moderna patented a 19-nucleotide sequence back in 2016 that was eventually discovered on the furin cleavage site of the SARS-CoV-2 spike protein. The National Institute of Allergy and Infectious Disease (NIAID) approved coronavirus gain-of-function research in Wuhan for years in the lead-up to the covid-19 scandal. This controversial research included chimeric human-rodent experiments to test immune responses.

The destruction of the scientific method and medical ethics continues

On December 31, 2019, a pneumonia of “unknown etiology” was discovered in Wuhan City, Hubei Province of China, with 44 cases reported to the World Health Organization (WHO). Eleven of the cases were severe. On January 9, 2020, WHO determined that the pneumonia outbreak in Wuhan, China was the result of a new causative agent – SARS-CoV-2, yet the origins of this causative agent remained unknown. From that point forward, governments, medical authorities, and corporate media around the world began advertising new terms, “coronavirus,” “covid-19” and “covid.” An apocalypse of terror, scientific fraud, and medical tyranny would come next.

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Already in place was a predatory vaccine development program that relied on the intentional release of a bioweapon and subsequent lock downs, fraudulent PCR swabs, persistent disease marketing, and further acts of medical tyranny and disease theater. Governments around the world deprived individuals of civil liberties and threatened their inalienable rights, all to force these predatory mRNA experiments onto the masses. The corporate media played their role, terrorizing people’s minds and advocating for lockdowns, mandates, and mass formation psychosis. Medical authorities suspended the informed consent principle, withheld efficacious treatments, separated families, and coerced individuals to take part in an experiment that consisted of numerous human rights violations.

The emergency declarations that were initiated by governments around the world ultimately opened the door for mass science fraud, money-laundering, propaganda, and censorship — destroying scientific integrity and allowing vaccine companies to conceal vaccine injuries recorded in rushed clinical trials.

Under U.S. President Donald Trump, Operation Warp Speed unleashed a new era of pharmaceutical racketeering, designating billions in taxpayer funds to develop a vaccine that promised to prevent and eradicate covid-19. OWS mobilized the federal government, the Department of Defense (DOD), and all the branches of the Department of Health and Human Services (HHS).

Lock downs were put in place to force compliance. Bodily mandates were used to prime the public to accept a “vaccine” as their lord and savior — some altruistic ticket to freedom. Since the vaccine’s hasty release, over 613 million doses of experimental mRNA were injected into the public, encoding spike proteins in human cells that would go on to pollute their blood, cause inflammation, and concentrate in distal organs, while shedding through the skin and aerosols, driving the evolution of new variants. The results of this coercive vaccine program have been an abysmal failure, leading to the approval of multiple booster doses of mRNA updates to supplant failing immunity in the population. These spike proteins have affected people in different ways, causing inflammation of the cardiovascular system, blood clots, neurodevelopment disorders, strokes, miscarriages, cancers, antibody dependent enhancement, among other forms of immune depletion.

RSV experiments, antibody dependent enhancement, and the abuse of children

Now the vaccine makers are subverting any last shred of medical ethics and scientific integrity to approve new mRNA jabs for a host of other afflictions. Penn Medicine sees the mRNA technology as the future of vaccines for “every imaginable infectious disease.” Pharmaceutical companies are working on mRNA vaccines for heart attacks, heart failure, strokes, and neurodevelopment disorders. All these health problems were caused or exacerbated by the initial spike protein mRNA vaccine experiment. Notwithstanding, mRNA experiments are in the works for flu, covid variants, and RSV. The severity of these respiratory diseases continues, thanks to antibody dependent enhancement caused by the current vaccine supply.

A study published in Nature Microbiology, titled, “Antibody Dependent Enhancement and SARS-CoV-2 Vaccines and Therapies” highlights how ADE worsens the severity of RSV in children. In Pfizer and Moderna’s own clinical trials, the COVID shots caused vaccine recipients to suffer from RSV FOUR TIMES more frequently than those who received a placebo. The vaccinated group also suffered from pneumonia, while the unvaccinated did not. Previous attempts at RSV vaccines have failed miserably. None of this matters to the FDA, which recently granted Fast Track designation for mRNA-1345, Moderna’s investigational single-dose mRNA vaccine encoding proteins for respiratory syncytial virus (RSV).

When will the cycle of fraud and abuse be put to an end?

Sources include:

UndercoverDC.com

NaturalNews.com

NaturalNews.com

Telegraph.co.uk

WHO.int

NaturalNews.com

NaturalNews.com

NaturalNews.com

Nature.com

VigilantFox.substack.com

FierceBiotech.com

WebArchive.org

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