Reviewing c19=Bioweapon Patent evidence [Kingston]

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So, I spent Christmas and Boxing Day, and every day since (it’s now the 29th of December and I’m still going…) downloading, highlighting, and finally going through all the “Karen Kingston patent evidence” that SARS-Cov-2 is an AI bioweapon. How about you? lol. I hope your life isn’t as nerdy as mine and you were able to enjoy spending time with your loved ones. I also hope you were able to share some truth along the way and save some lives in person (I know it’s hard). xo

Still a Work-in-Progress.

First published: December 29, 2022

First up, Karen’s research is based on what “Moderna and Pfizer’s patents, their own websites, and documents, as well as various related studies, say.“ She’s explaining what their actual documents say they can do.

Whether they can actually do what they say they can is still to be determined, but what you get from Karen’s research is “what the manufacturers themselves say they can do.”

Of course, the patents and documents themselves could be propaganda or a marketing tool—we’re talking ‘trillion-dollar” criminal companies here, with “trillions” of reasons to exaggerate and lie to gullible shareholders (history already shows they’ve repeatedly done this time and time again).

But her research (as a bioanalyst—who does this kind of research for a living—in other words, this “is” her expertise) into the patents is what their own “paperwork” says they can do—and, since some of their own documents seem to be matching up with what seems like self-assembling circuitry-like objects being found in the blood of everyone (vaccinated or not) and being published by alarmed scientists and blood-analysts all over the world, we should review the research seriously rather than automatically disregard it, because if we dismiss this evidence and we’re wrong, we don’t stand a chance at saving anyone. Until we lay out ALL the evidence that all the good researchers around the world are coming forward with, each with their own specific expertise and background, we shouldn’t be dismissing anyone at this point, particularly one of the few that is literally showing the companies’ own documents!

I wanted to have a “text-only” version of her evidence laid out while at the same time reviewing each patent/study and taking screenshots/highlights, etc. So this post is just for me to “lay it all out for me to get my head around it all.”

I suggest you view her substack for the image references along with her report, because I’m pretty close to living under a bridge and cannot afford her “paid” subscription, so a lot of the evidence that she only shares with premium subscribers may be missing from my notes. (I will try and figure out what’s missing via her videos.)

I’ve also got a post dedicated to the various “suspicious patents” that I’ve saved over the past few years trying to understand this whole thing. (The downloadable-folder on that post is where I have taken my own screenshots and highlighted text of any patents.)

Click to expand
Show less

Here are some quotes that give us a pretty good overview of what her evidence focuses on:

“The SARS-CoV-2 mRNA virus was never deadly, nor was it contagious. I can’t emphasize this enough, it wasn’t SARS-CoV-2 that caused COVID-19. COVID-19 disease, disabilities and death are the product of AI bioweapons.”

Karen Kingston

“SARS-CoV-2 ‘spike proteins’ are not biological proteins produced by cells in the human body. SARS-CoV-2 ‘spike proteins’ are smart magnetic hydrogels encapsulated in PEGylated lipid nanoparticles (LNPs). Spike proteins are Ai bioweapons that are a greater threat to humanity than a nuclear bomb.“

Karen Kingston

“The NIH/ EcoHealth ’s mRNA GOF-research funded the development of parasitic Ai bioweapons (mRNA Qdot) that are delivered in advanced lipid nanoparticle technologies and can inoculate (infect) animals and humans through aerosol sprays and contamination of gels, food, and beverages, as the DARPA proposal states.”

Karen Kingston

Patents

The technology for all mRNA COVID-19 vaccines uses lipid nanoparticle (LNP) technology. (KK)

Video Rundown - Patent Evidence

Here is the best, most complete, and least-interrupted presentation I’ve seen on her patent evidence, and I’ll also cobble together some clips for any missing/additional info she reveals in newer videos as she continues her research:

Rumble | BitChute

– Covid-19 injections contain NEUROWEAPONS embedded in Lipid Nanoparticels (LNP)
– Neurological weapons were hidden through Emergency Use Authorization cover-up
– Shocking patents confirm it’s all true (patent numbers shown)
– Transhumanism assault on humanity now under way, people becoming LESS human
– LNPs can be activated via 5G frequencies to achieve physiological changes
– Covid “vaccines” appear to be exotic tech INSTALLED in human hosts
– CCP-linked AI company named “national security threat” in USA
– 5G infrastructure to be exploited by AI embedded systems for surveillance
– Post-vaccine “biostructures” are self-assembling biosynthetic weapons
– Patents reveal shocking nature of “spike protein” structures in vaccines
– Hybrid structures demonstrate “cognitive action” capabilities
– Described in patents as “intelligent sensor platforms” that carry out instructions
– So-called “spike proteins” seen in electronic microscopy are actually these nanotech platform structures
– They are small enough to enter nervous system cells and alter their behaviour
– More details on quantum dots used by the US Army, combined with carbon nanotubes

I went through and downloaded several of her December patent videos, and she seems to add a new key point for each one, so I spliced together a few of the interviews to have at least one video that covers them all. (Interviews included: Karen Kingston with Brannon Howse, Maria Zeee, Greg Hunt (USA Watchdog), Stew Peters, Jeff Dornik (Foxhole), Martin Bernstein (LivingLiberatorsAlliance-all963), Reiner Fuellmich (ICIC), and Mike Adams (Natural News). Because I don’t have time to be a full-time editor, this video that I spliced together may cross-over the patents a few times, but I wanted to make sure that I had one video that covered “EVERYTHING” so that I had at least one post that contained all of her evidence.

US10703789B2 - MASTER Moderna Patent

US10703789B2 (01)

The “MASTER” Moderna patent

(built on 90 patents)

  • Section 219, the lipid nanoparticles (LNPs) are fully programmable self-assembling technologies.
  • Sections 219 and 220 state that the LNPs can contain gels and hydrogels.

The functionality of the nanotechnology in the COVID-19 bioweapon injections to ensure rapid, easy, and targeted biodistribution of the nanoparticles throughout the body.

Karen Kingston

US20120228565A1 (Sub of Master) Dispersible Metallic nanoparticles

US20120228565A1 (02)

‘Enhanced dispersible Metallic nanoparticles’

Life Technologies > Acquired by ThermoFisher > 15 yr contract with Moderna

Patent US20120228565A1 expired on May 16, 2022 due to nonpayment. Life Technologies is listed as the correspondent contact. The address shown is an address for one of the ThermoFisher Scientific offices in Carlsbad, CA. The original applicants’ names, Edward William Adams and Marcel Pierre Bruschez, Jr., are listed as unavailable. (KK) Life Technologies was acquired by Thermo Fisher Scientific in January, 2014 (03)

On February 23, 2022, ThermoFisher Scientific announced a 15-year manufacturing deal with Moderna for Moderna’s mRNA COVID-19 vaccines and other experimental mRNA vaccines. ThermoFisher Scientific had previously partnered with Moderna to manufacture their mRNA COVID-19 vaccines in 2021. (04)

Karen Kingston

  • US 0028565 A1 is part of the intellectual property of the MODERNA master patent and is for water-dispersible semi-conductive metallic nanoparticles.
  • Section 3 quantum dot’s functionality is based on the quantum mechanics of the Bohr particle.

Due to quantum mechanics, quantum dots that have been injected into global citizens by means of the the COVID-19 bioweapons and can quite literally appear within the human body based on specific electromagnetic frequencies (EMF) or disappear based on specific frequencies.

Karen Kingston

WO2012148684 (Sub of Master) Opal Hydrogels

WO2012148684 (05)

Opal hydrogels: part biology and part technology

WO 148684 A1 is part of the intellectual property of the MODERNA master patent, and is for opal hydrogels. Opal hydrogels are part organic and inorganic.

Opal hydrogels look like quantum dots. “They have this bright blue and rainbow colours they give off,” 

Karen Kingston

  • Part technology – AI, metallic structures.
  • Part biology – genetic sequences from other life forms e.g., insects, reptiles, rodents. 

This hybrid biosynthetic technology species is Inorganic-Organic Hydrogels (IOHs).

Quantum dots are part of the technology in the IOH hydrogels and emit vibrant colours. (Quantum dots are also what give LED television screens their bright colours.)

US 02510618 A1 (Sub of Master) Carbon Nanotubes owned by Chinese Military

US 02510618 A1 didn’t come up in my patent search, but US20130251618A1 has the same title and seems to be the same one she’s referring to.

US20130251618A1 (06)

Relies on Carbon nanotubes patent owned by Chinese Military

Another patent on which the master Moderna patent is based is one owned by the Chinese military and relating to carbon nanotubes.

Quantum dots need to be encapsulated in single wall carbon nanotubes (SWCNT) within the mRNA lipid nanoparticle (LNP) technology to be delivered into the human body.

Karen Kingston

US20120228565A1 - ThermoFisher QDot® (ThermoFisher has a 15-year mRNA contract with Moderna)

US20120228565A1 or US8691384B2 (10) (11)

ThermoFisher QDot® patent

ThermoFisher > 15 yr contract with Moderna

Section 32 – ThermoFisher Scientific branded and registered trademarked all quantum dots, semiconductor nanocrystals, and nanocrystal technologies as Qdot® (12) .

ThermoFisher Scientific (Life Technologies) is the owner of the intellectual property (IP) described in US Patent 0228565 A1. Allowing the patent to lapse results in the Qdot® intellectual property becoming a trade secret.

Qdot’s primary mRNA functions are to perform gene editing directly inside human cells INSIDE THE HUMAN BODY. Qdot® (quantum dots) are in the COVID-19 vaccines. ThermoFisher Scientific’s QDot® patent provides details on how.

Karen Kingston

  1. Qdot®creates an ionic charge to penetrate the cell wall and nucleus of cells.
  2. Qdot®uses FISH and SERS to target, extract, analyze, and sequence cells’ DNA.
  3. Qdot® performs gene-editing inside human cells using CRISPR (mRNA, siRNA) and other gene-editing technologies to delete and replace partial gene sequences in order to permanently alter the DNA of cells inside of our bodies and the human genome.
  • Semiconductor Nanotechnologies (section 3)

Nanotechnologies made with graphene oxide, such as the single-walled carbon nanotubes (SWCNTs) that encapsulate QDot®, are semiconductor technologies.

Semiconductor nanotechnologies can conduct and host electromagnetic fields (EMF), and are strong receptors for electromagnetic pulses (EMP) signals and EMP attacks.

Graphene oxide also has tremendous strength (50% stronger than titanium, 400% stronger than aluminum) and can be as thin as one-atom thick (1/10 of a nanometer). (13)

Karen Kingston

  • Emits electromagnetic radiation (section 33)

Qdot® emits ultraviolet and infrared radiation. This can cause cell death, cancer, and even microwave radiation inside the body. Qdot® targets and labels organs, tissues, and cells inside the human body.
Each person who received a COVID-19 ‘vaccine’ received trillions of Qdot® injections.

Karen Kingston

Qdot® also utilizes FISH (fluorescent in situ hybridization) to target DNA and RNA sequences in cells. FISH uses fluorescent DNA probes to target the precise cellular locations of a genetic sequences within cells. (section 109)

After cells inside the human body are targeted by FISH and Qdot®, Qdot® utilizes CRISPR to perform actual gain-of-function mRNA gene editing of cells and viruses inside our bodies. (comparing study to section 42) (14)

Karen Kingston

The inside-the-human-body-gene-editing functions of mRNA Qdot® include translation and transfection.

When “the experts” told us that GOF mRNA viruses, including SARS-CoV-2, are capable of human-to-human transmission or that COVID-19 “vaccines” could not genetically edit the DNA of our cells or the human genome, they were lying.  (15)

Karen Kingston

mRNA Qdot® delivers mRNA directly into a cell’s nucleus to integrate foreign DNA (new genetic sequences) into a cell’s genome.

Per ThermoFisher Scientific’s patent, Qdot® is able to successfully perform in vivo (inside the body) genetic editing of human cells by utilizing SERS (Surface Enhanced RAMAN Spectroscopy). The SERS probes are DNA nanoprobes that are made of metal alloys such as gold, copper, platinum, aluminum, silver, palladium, etc.

Karen Kingston

  • Study: Application of the amplification-free SERS-based CRISPR/Cas12a platform in the identification of SARS-CoV-2 from clinical samples. (16)

Qdot® enables SERS metallic nanoprobes to utilize CRISPR technology in order; to sequence the DNA from the nucleus of a cell; delete targeted gene sequences; and then replace the deleted sequences with new genetic sequences in order to transform global citizens and our children into the new hybrid human species.

Karen Kingston

  • (section 109) "Without limiting the scope of the present invention, nanoparticle conjugates can comprise nanocrystals associated with individual nucleotides, deoxynucleotides, dideoxynucleotides or any derivatives and combinations thereof and used in DNA polymerization reactions such as DNA sequencing, reverse transcription of RNA into DNA, and polymerase chain reactions (PCR)."

PCR tests are testing for successful DNA Ai-human-hybridization. PCR tests are for collection of our genetic data for purposes of genetic experimentation and extermination of US civilians and military.

Karen Kingston

  • Study: Qdot® enables the physical (adsorption) and genetic integration of metals into human cells. Cells infected with COVID-19 mRNA lipid nanoparticles (LNPs) are no longer human cells. Human cells inside our bodies will go through a process of apoptosis (cell death) and the Qdot® powered Ai nanogel will take over the cell functions and structures. (17)

Info: Quantum dots are invisible

Quantum dots are invisible

Quantum dots are less than 1/100th the size of a micron. (Most viruses are several microns in size). While quantum dots cannot be seen with the naked eye, their effects are not ‘invisible’ to our bodies.

The electromagnetic fields and frequencies emitted by quantum dots can cause emotional, psychological, and physical disease and dysfunction in our bodies. Quantum dots can be used as neuroweapons, disrupting your emotions, energy, physical abilities, and ability to think clearly (brain fog).

It is evident that the COVID-19 injections contain nanotechnology that can host electromagnetic fields and receive signals. People are magnetic and are suffering from rapid onset of neurological disorders and hallucinations, sometimes resulting in death.

Scientists and researchers have observed the self-assembling nanotechnology by examining the ingredients of the COVID-19 vials under an electron microscope.

  • Use of quantum dot technology in humans is regulated by the Centers of Devices & Radiological Health ( CDHR ) of the FDA because they are electronic devices that emit radiation. (KK)
  • Per the 2011 book publication, Quantum Confinement Effect, quantum dots are able to produce electromagnetic labels (i.e. Bluetooth addresses) inside the body and tag organs and extensive animal research has been successfully completed using quantum dots to invade, target, and mark major organs, such as the heart, lungs, kidneys, liver, spleen, and brain. (KK)
  • Per ThermoFisher Scientific’s website, quantum dot (Q-dot labels) can be used to target, track and trace, not only tissues, but even individual cells. (KK)
  • A peer-reviewed article published by Wiley Online Library clearly states that the “backbone, the energy source, the technology between inorganic and organic –  the inorganic-organic hybrids – is Qdots, it’s quan[tum] dots,” (KK) (18)

Info: LNPs are the actual Bioweapon

LNPs enable the mRNA gene-editing technology to invade the lipid bilayer of cells and then infect, replicate, and produce biosynthetic proteins and other mRNA-sequence-instructed biosynthetic structures. To put the magnitude of the pure evil genius of the LNP technology into perspective, mRNA was not able to infect any cells, including human cells, due to a four-billion year evolved lipid bilayer that protects cells, all cells, until this technology was invented. The lipid nanoparticle (LNP) technology is pure evil. LNPs are also considered biotagging neurotechnologies and nanoweapons, that happen to look exactly like COVID-19 spike proteins. (Karen Kingston)

Info: Graphene, Quantum dots, hydrogels and nanoparticles are already in everything

“For more than a decade, nanotechnologies such as quantum dots, hydrogels, graphene oxide, and single wall carbon nanotubes (SWCNT) have been used in consumer electronic devices, healthcare products, foods and beverages, military neuroweapons, and medical device research and applications.”

Info: SARS-Cov-2 is a psyop - weapon is nanotech (not a virus)

“The narrative that the novel SARS-CoV-2 ‘wild type’ or mRNA virus hijacks cells to biologically produce spike proteins, thereby causing inflammation and disease, is a deceptive and false gaslighting strategy that has led to the disease, disabilities, and deaths of millions of adults and children around the world. Citizens were duped into believing there was a highly infectious virus that produced lethal spike proteins. This deceptive narrative was required to instil fear and blind trust in order to successfully launch the COVID-19 War on Humanity, including global acceptance of the lethal COVID-19 bioweapon shots. The SARS-CoV-2 virus and spike protein story is a psyop (psychological operation) in military terms.”

Video Rundown - weapon is nanotech found in everything (not a virus)

AI Biosynthetic parasites (COVID and Vax) are a hybrid of biology and technology. Anti-parasitics can slow down the replication of the biology-side, and there are EMFs that can disable the technology-side.

Rumble December 18, 2022 “Proof COVID is a Nano weapon parasite”

I normally don’t watch Stew Peters because it’s difficult to post anywhere and be taken seriously, but this is the best summary I found out of all the Karen Kingston videos I downloaded these past few days (to deep-dive into her patent evidence) that includes the actual “spike protein” “SARS-CoV-2” stuff and what is making people (everyone) sick.

Slides

Found some of her slides here and here, and some 2021 images here.

Links and Studies

  • https://karenkingston.substack.com/
  • Letter: DARPA Proposal Whistleblower: Major Joe Murphy, Office of Naval Research
  • Study: Application of the amplification-free SERS-based CRISPR/Cas12a platform in the identification of SARS-CoV-2 from clinical samples
  • Study: Cells infected with COVID-19 mRNA lipid nanoparticles (LNPs) are no longer human cells
  • Study: Fluorescent Inorganic-Organic Hybrid Nanoparticles
  • Study: A Novel Graphene Quantum Dot-Based mRNA Delivery Platform
  • Study: Application of the amplification-free SERS-based CRISPR/Cas12a platform in the identification of SARS-CoV-2 from clinical samples
  • Study: Acidic pH-responsive nanogels as smart cargo systems for the simultaneous loading and release of short oligonucleotides and magnetic nanoparticles
  • Study: Fluorescent Inorganic-Organic Hybrid Nanoparticles

Who is Karen Kingston?

Karen Kingston

Karen Kingston is a pharmaceutical and medical device business analyst. She has over 20 years of experience in business development, marketing, sales, public speaking, and strategic consulting. As an executive strategist, her clients range from start-ups to Fortune 500 leaders, including Allergan, Pfizer, Johnson & Johnson, Medtronic, and Thermo Fisher Scientific. She has developed key messaging, business plans, pricing strategies, global campaigns, go-to-market strategies, and other core marketing assets for inline products and blockbuster launches.

She began her career as a top performing Pfizer sales representative in NYC and was quickly recruited to the marketing side of the business. She played an integral role in the re-launch of VIAGRA shifting the focus to younger men and empowering patients to speak to their doctors about Viagra. She has led sales training, marketing and communication workshops and has appeared on FOX, MSNBC, and CBS as the spokeswoman and Director of US Marketing for InnoVision Labs.

In 2007, Karen founded Varitage. She specializes in improving lead generation, nurturing, and conversion for B2B and B2C customers. Karen works closely with her clients and team to provide actionable insights to make real-time, well-informed strategic decisions that result in significant improvements across critical marketing KPI’s.”

The following timeline may not make sense unless you've first watched the following presentations:
Video 1: Patent Evidence Presentation (Rumble)
Video 2: Covid-19 weapon is nanotech (not a virus) (Rumble)

SARS Unable to Infect Humans
Dr Ralph Baric

In 2015, Ralph Baric, the inventor of the SARS-CoV-2 mRNA virus, recognized that mRNA coronaviruses were useless on their own.

He clearly states that mRNA coronaviruses (including SARS-CoV-2) are not of ‘epidemic potential,’ stating that even if humans were infected with SARS-CoV-2 via a direct, man-made delivery mechanism, human-to-human transmission was proven to be impossible.

Rumble (21mins)

Dr Ralph Baric - SAR-like WIV1-CoV Not capable of human-to-human transmission (Click to Expand)

SAR-like WIV1-CoV Not capable of human-to-human transmission

2015 Ralph Baric, PNAS “SARS-like WIV1-CoV Poised for Human Emergence,” recognizes that his coronavirus mRNA viruses are not capable of significant human-to-human transmission, if any transmission at all. (19)

“WIV1-coronavirus (CoV) cluster…may undergo limited transmission in human populations… in vivo attenuation (attenuation means that SARS-CoV-2 becomes extremely weak once inside the human body) suggests additional adaptation is required for epidemic disease.”

mRNA too fragile to infect cells
mRNA Scientists

mRNA lab experiments have historically failed because the mRNA invention is so fragile and unstable on its own. The "fragile mRNA molecules" used in the COVID-19 vaccines’ is the SAR-CoV-2 GOF mRNA virus.

Nature Biotechnology “Overcoming Cellular Barriers for RNA Therapeutics in RNA,” RNA gene-therapies, including mRNA, are unable to infect cells, any cells, due to billions of years of an evolutionary defense mechanism, the lipid bilayer. (20)

Overcoming cellular-billionyears
Nature
Moderna, NIH, NIAID, Carnegie, Sanofi

C&EN article interviewing mRNA experts from Moderna, NIH, Carnegie Mellon, Sanofi. et al.; and the inventors of the WIV-1 SARs-CoV-2 spike protein GOF mRNA sequences (Barney Graham from the NIAID and Jason McLellan from Moderna), the author summarizes these mRNA experts’ opinions:

“Fragile mRNA molecules used in the COVID-19 vaccines can’t get into cells on their own. They owe their success to lipid nanoparticles that took decades to refine.” (21)

mRNA Scientists - mRNA unable to infect cells without LNPs (Click to Expand)

lipidshells
C&en

Dr. Kathryn Whitehead, “We don’t even screen (mRNA) in vitro anymore. I find it more informative to test (mRNA) directly inside the animal”

“The devil is absolutely in the details as far as LNPs are concerned,” Ciaramella, former head of infectious diseases at Moderna.

“mRNA is incredibly delicate. Enzymes in the environment and in our bodies are quick to chop mRNA into pieces, making lab experiments difficult and the delivery of mRNA to our cells daunting.”

“People used to say that if you looked at it wrong it would fall apart.” ~ Frank DeRosa, who began working with mRNA in 2008 and is now chief technology officer at Translate Bio, a firm developing mRNA vaccines with Sanofi.

DARPA Proposal
Daszak, Baric, Shi, EcoHealth, DARPA

January 2018, Peter Daszak reached out to DARPA for funding via a proposal. In EcoHealth Alliance’s submission, Baric and Shi were listed as EcoHealth Alliance’s team members to develop the chimeric gain-of-function spike protein bioweapons from the mRNA coronavirus library the team had already created.

Daszak also states they are going to infect the "bats" by delivering the lipid nanoparticle (LNP) technology encapsulated spike proteins in the form of a transdermal (skin) patch, a gel for the bats to eat, a gel for their skin, or inhaled aerosol sprays.

The DARPA proposal states that they are going to infect the bats with, “aerosolization sprayers designed for cave settings; and automated sprays triggered by timers and movement detectors at critical cave entry points.”

Per the DARPA proposal, the next phase of their bioweapons research was focused on how to take Baric’s virtually useless mRNA gain-of-function coronaviruses (by his own admission) to create something from his mRNA viruses that was infectious, deadly and of ‘pandemic potential’.

The 2018 EcoHealth Alliance DARPA proposal clearly states, “WE WILL DEVELOP recombinant CHIMERIC SPIKE-PROTEINS from known SARSr-CoV …AND INCORPORATE THEM INTO NANOPARTICLES…”

Karen claims (in the first video in this post) that "Bats" is a code-word for humans.

EcoHealth's DARPA proposal documents and links (Click to Expand)

EcoHealth’s DARPA proposal

Peter Daszak and the EcoHealth Alliance (EHA) proposed injecting deadly chimeric bat coronaviruses collected by the Wuhan Institute of Virology into humanised and “batified” mice.

The EcoHealth (EHA) / Wuhan Institute of Virology (WIV) proposal (named ‘DEFUSE’) was ultimately rejected by DARPA for full funding (but leaving open the door for partial funding), in part because it mis-interpreted the gain-of-function guidelines.

project-defuse
  1. Download all Project DEFUSE Documents (22)
  2. DRASTIC Analysis of the DEFUSE Documents (23)
  3. DocumentCloud copy (24)
  4. PDF 1: A brief DRASTIC Analysis of the EcoHealth Alliance DEFUSE Proposal (25)
  5. PDF 2: The Reasons why the DEFUSE Proposal was Rejected by DARPA (26)
  6. Major Joe Murphy, Office of Naval Research, Letter re: EcoHealth’s DARPA proposal (27)
  7. Origins of SARS-CoV-2 (Dec 19, 2022) (28)
  8. The Intercept “The proposal, rejected by U.S. military research agency DARPA, describes the insertion of human-specific cleavage sites into SARS-related bat coronaviruses“. (29)
  9. Igor Chudov: Sars-Cov-2 was Lab Made Under Project DEFUSE (30)
  10. U.S. Right to Know’s efforts calling for COVID-19 origins investigation (31)
  11. University of Sydney’s involvement in the COVID-19 Coverup (32)

Prof. James Giordano
Weaponized Aerosolized nanoparticles

Per a 2018, West Point lecture given by Professor James Giordano at the Modern War Institute, lipid nanoparticles (LNPs) have been used as nanoweapons to emotionally and mentally hijack influential leaders and can be used to induce a pandemic of ‘worried well’ or ‘pandemic of strokes.'

“Nano-scale Aerosolized Bio-Weapons that can remote-control your body & mind”

KK-James-Giordano
James Giordano at Modern War Institute
Prof. James Giordano at the Modern War Institute (Click to Expand)

“Nano-scale Aerosolized Bio-Weapons that can remote-control your body & mind”

More from Prof. James Giordano (including alt platforms if you can’t see the Rumble video):

SARS-CoV-2 not transferrable
Wuhan Hospital Workers

The lack of human-to-human transmission is further validated by real world evidence data of hospital workers’ infection rates at the hospital next to the Wuhan Market. The hospital worker infection rate at ground zero was 0.000%.

Hospital workers from Wuhan never got infected. Experts who proclaimed that COVID-19 was or is a highly-infectious virus were making false statements not based in real world evidence.

Hospital workers from this Wuhan study never got infected (Click to Expand)

Hospital workers from this Wuhan study never got infected

December 2020 Immunity, Inflammation, and Disease – 191 Wuhan hospital workers who were tested for SARS-CoV-2 antibodies via throat swabs and blood work. All tests came back negative. Two-hundred and twenty-two (222) hospital workers also had chest X-rays. All chest x-rays came back clean.

Surveillance of SAR

PCR False Positives up to 97%
CDC

The CDC intentionally misled the public into believing that SARS-CoV-2 was capable of human-to-human transmission.

According to CDC data published on December 15, 2021, the emergency use authorized (EUA) PCR-tests used throughout 2020 and 2021 produced up to 97% false-positive results.

The phony SARS-CoV-2 EUA PCR tests were critical "theatre props" in convincing us that the COVID-19 story was true.

CDC data - PCR False Positive Dec 2021 (Click to Expand)

Cdc false positive
Cdc false positive plos

Although I know PCR is a fraudulent test as I’ve spent a lot of time on it and have many posts as well as unfinished presentations in the works to show people, as well as an entire whiteboard filled with it (like a crazy person) to make sure any visitors to my house see the entire PCR-scam which is so crucial for getting out there… that being said, I don’t think this study she listed is proof that the CDC data shows 97% false positives with the PCR test. i.e. I think using this particular study is good for showing evidence the EUA kit has 97% false positives to n3 which is what it states… which means she should also state that – because we have to be exact with our knowledge and evidence, not sneaky or biased or one-sided if that makes sense? If you want to state it’s 97% false positives, you would have to produce the evidence, and this ain’t it. Or, seeing as she is a bioanalyst and I would assume know the literature better than me, if this document really does prove that it’s 97% false positives, then she needs to explain it where there is no doubt.

C-19 Vaccines contain LNPs
FDA Submissions

Per the August 23, 2021, FDA approved biological license application for PFIZER’s COVID-19 vaccines:

“COMIRNATY contains mRNA of SARs-CoV-2 that is formulated in lipid (nanoparticles).”

Rumble (8mins)
FDA Submissions

REF?

FDA Filings and Karen Vids discussing it (Click to Expand)

[ICIC Clip] Karen Kingston explains how the Polyethylene glycol (PEG) is an experimental device (Rumble)

See also: Karen Kingston refuting claim that there is no nanotechnology in the jabs – it’s literally in their FDA filings. (Rumble)

Rumble (4mins)

  • Need to hunt down the FDA filing links again, particularly the new one that apparently got approved “COMIRNATY”

mRNA for all jabs
Whitehouse Executive Order for mRNA

US President Joe Biden signed an Executive Order on September 12 , 2022, calling for an ‘all of government approach’ to ensure the bodies of Americans will be installed with genetic engineering technologies. (Trump signed same order in 2017)

Executive Order

“We need to develop genetic engineering technologies and techniques to be able to write circuitry for cells and predictably program biology in the same way in which we write software and program computers… ”

IN PROGRESS
I am still working on this post

THIS is taking a lot longer than I expected, but I'm going to keep working on it until it's done. I'll publish now to at least raise awareness of her work, and will keep going every day until I am up-to-date. I haven't fully referenced it yet, either, but I will as I go through the documents.

Click to Expand

People & Companies mentioned in this post

  1. Charles Lieber, his father Robert Lieber, and his grandfather
  2. Bill Gates and his father
  3. Ralph Baric
    • University of North Carolina.
    • Funded by Anthony Fauci’s NIAID/NIH (received over $100 million for coronavirus research)
      • Coronavirus mRNA gain-of-function research and chimeric spike proteins.
        • Named inventor on dozens of patents for coronaviruses, chimeric spike proteins, and other gain-of-function bioweapon-based technologies.
      • Works with Peter Daszak and Zhenghli Shi
  4. Anthony Fauci and his ancestry
  5. President Joe Biden and former President Donald Trump
  6. Pirbright Institute
  7. Peter Daszak
  8. Dr. Zhenghli Shi
    • of the Wuhan Institute of Virology (WIV) who works with EcoHealth Alliance
  9. DARPA (Defense Advanced Research Projects Agency)
  10. Barney Graham from NIAID/NIH (patent WIV-S-2P spike and other S-2P spike proteins)
  11. Jason McLellan from University of Texas (patent WIV-S-2P spike and other S-2P spike proteins)
  12. CDC
  13. FDA
  14. GenBody (NIH funded genetic-research study conducted by GenBody, South Korea, collecting DNA from schools in USA during pandemic under the guise of PCR-testing)
  15. Moderna
    • Inventors: Antonin de Fougerolles and Justin Guild (patent Modified polynucleotides for the production of secreted proteins)
    • ThermoFisher (patent Method for preparing surface-modified semiconductive and metallic nanoparticles having enhanced dispersibility in aqueous media)
  16. Joe Qiu – Program Manager at Army Research Office
  17. Karen Kingston – biotech analyst with more than 20 years of experience.
  18. Thomas Renz – Lawyer
  19. Reiner Fullmich – Lawyer
  20. Professor James Giordano
  21. Dr. Kathryn Whitehead – head of Chemical and Bioengineering at Carnegie Mellon
  22. Dr Andrew Huff – former VP EcoHealth Alliance, Whistleblower
  23. Pfizer
  24. Dr Carrie Madej – osteopath and internist, transhumanism whistleblower

And: Graphene | PEG | Quantum Dot | Patents | Transhumanism | Bioweapon

References[+]

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