BREAKING BOMBSHELL: What the Next “Pandemic” Will Look Like

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by 2nd Smartest Guy in the World, 2nd Smartest Guy in the World:

“That, you know, I’d say— ah— will get attention this time.”

— Bill Gates

The democidal maniacs are ramping up their followup COVID-19 fear-mongering, but that will merely serve as their ingenious head fake.

The next “pandemic” will be one that scant few are expecting, with the requisite brand new Modified mRNA DEATHVAX™ offerings.

TRUTH LIVES on at https://sgtreport.tv/

The PSYOP-23 Followup

This upcoming outbreak will be the Nipah virus, which is yet another lab created bioweapon brought to us courtesy of the Gain of Function all-star team of Fauci, Gates, NIH, CIA, DoD, Pentagon, CFR, UN, WHO, WEF, Rockefeller Foundation, the Wuhan Institute of Virology, et al.

According to a research study from 2021 entitled, Nipah virus vector sequences in COVID-19 patient samples sequenced by the Wuhan Institute of Virologythe latest franken-virus was sequenced at the very same lab that released C-19:

We report the detection of Nipah virus in an infectious clone format, a BSL4-level pathogen and CDC-designated Bioterrorism Agent, in raw RNA-Seq sequencing reads deposited by the Wuhan Institute of Virology (WIV) produced from five December 2019 patients infected with SARS-CoV-2. Research involving Nipah infectious clones has never been reported to have occured at the WIV. These patient samples have been previously reported to contain reads from several other viruses: Influenza A, Spodoptera frugiperda rhabdovirus and Nipah. Previous authors have interpreted the presence of these virus sequences as indicative of co-infections of the patients in question by these pathogens or laboratory contamination. However, our analysis shows that NiV genes are encapsulated in synthetic vectors, which we infer was for assembly of a NiV infectious clone. In particular, we document the finding of internal N, P-V-W-C and L protein coding sequences as well as coverage of the G and F genes. Furthermore, the format of Hepatitis D virus ribozyme and T7 terminator downstream of the 5-prime end of the NiV sequence is consistent with truncation required at the end of the genome for a full length infectious clone. This indicates that research at WIV was being conducted on an assembled NiV infectious clone. Contamination of patient sequencing reads by an infectious NiV clone of the highly pathogenic Bangladesh strain could indicate a significant breach of BSL-4 protocols. We call on WIV to explain the purpose of this research on infectious clones of Nipah Virus, the full chronology of this work, and to explain how and at what stage of sample preparation this contamination occurred.

Mockingbird MSM Seeding

According to the Wall Street Journal, Indian Officials Rush to Contain Outbreak of Deadly Nipah Virus:

Authorities in southern India have ramped up testing and contact tracing for the Nipah virus following two deaths. Health experts said the virus is less contagious than Covid, but has a higher fatality rate.

Additional MSM doom hype came courtesy of a Forbes article last week entitled, What To Know About The Deadly Nipah Virus As India Races To Contain Outbreak:

Health officials in India’s southern state of Kerala are rushing to track and contain an outbreak of Nipah that has already killed two people and hospitalized three others. According to news reports, public health workers have tested hundreds of workers and schools, government buildings, religious institutions, public transport and public offices have been closed or suspended in at-risk areas to curb potential spread. It is the state’s fourth outbreak since 2018 and experts warn the area might be at particular risk from virus spillovers given the destruction of natural bat habitats by humans in the region.

NPR was told to write an article entitled, Another Nipah outbreak in India: What do we know about this virus and how to stop it?:

“The virus has an incubation period of 14-21 days,” says Anish. “Judging from the time of the secondary infections, we’re still in the middle of this outbreak,” he says. And there’s at least one piece of the puzzle that authorities still don’t know — How the patient Ali contracted Nipah in the first place.

Staggered Staged Multi-Deployments

What this means is that the Nipah virus has a higher rapid kill rate, or IFR (infection fatality rate), but will evolve far more quickly into a relatively benign virus; therefore, this “pandemic” will require sustained populace-wide aerosolized pulses, or deployments.

In other words, Nipah will have a slow build across “random” populations, exact quick death tolls, with staggered additional pulses across other seemingly random regions, and then reintroduced pulses concurrent with more new regional deployments to create the impression of a “sustained” and “worsening” global “outbreak.”

School Vector

This time the most effective “epidemic” vector will occur in schools, where traditionally non-existent IFR levels of immunologically robust children will be exploited to maximize the fear narrative; to wit:

WORLD WARNING: School Closures for Weaponized Viral Delivery Systems

WORLD WARNING: School Closures for Weaponized Viral Delivery Systems

Chris Sky came out with an important warning regarding school closures, and a new bioweapon “outbreak” targeting school aged children. He claims that an insider tipped him off to a plan to spread an aerosolized virus through school HVAC systems in order to perpetrate their followup PSYOP-23 “pandemic:”

Read full story

We also now know that BigPharma on behest of their Intelligence Industrial Complex handlers has been busy developing these complimentary Nipah “vaccines” since last year.

On July 11, 2022, Moderna and the National Institute of Allergy and Infectious Diseases (NIAID) began a clinical trial (NCT05398796) on a new mRNA vaccine for the Nipah Virus.

Now, a little over 1 year later, the media is ramping up their scare tactics for the Nipah virus, a virus that was identified 24 years ago (1999), and has caused isolated outbreaks in Africa and Asia.

Why did they feel it necessary to ramp up a clinical trial 1 year ago for a virus that has killed less than 200 people over the last 24 years, and that has been around since 1947?

Additional Nipah DEATHVAX™ Receipts

NIH launches clinical trial of mRNA Nipah virus vaccine

Dose Escalation, Open-Label Clinical Trial to Evaluate Safety, Tolerability and Immunogenicity of a Nipah Virus (NiV) mRNA Vaccine, mRNA-1215, in Healthy Adults

Never-Ending Simulations

And just like the tabletop and simulation exercises EVENT 201 and DARK WINTER, the same criminal players have been hard at work game planning the imminent Nipah “pandemic.”

In 2019 Johns Hopkins ran a tabletop exercise called CLADE X which references the Nipah virus:

The purpose of the exercise was to illustrate high-level strategic decisions and policies that the United States and the world will need to pursue in order to prevent a pandemic or diminish its consequences should prevention fail.

On March 14, 2022, four months before the clinical trial, The Gates Foundation announced a new $90 million funding initiative named Pandemic Antiviral Discovery (PAD):

Novo Nordisk Foundation, Open Philanthropy, and Bill & Melinda Gates Foundation Launch Initiative to Support New Antiviral Medicines for Future Pandemics

The focus of the first RFP will be henipavirus, a subfamily of paramyxovirus that includes Nipah virus—a pathogen with an estimated fatality rate of 40% to 75%.

Clearly, “Gates” is the most prescient man in the world when it comes to viral outbreaks and “vaccines;” except that we have incontrovertible proof as per the above 2021 research study that Nipah is a bioweapon.

Comparing Nipah virus to SARS-CoV-2, we know that both are enveloped, single-stranded RNA viruses that can cause severe respiratory illness in humans; however, they belong to different families: Nipah is a paramyxovirus, while SARS-CoV-2 is a coronavirus.

Nipah Virus and SARS-CoV-2 Similarities and Pertinent Features:

Cell Entry

Nipah virus enters cells through ephrin-B2 and ephrin-B3 receptors.

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