• Largest Covid-19 vaccine study yet finds links to health conditions
    Published: 12:31pm, 19 Feb, 2024

    Vaccines that protect against severe illness, death and lingering long Covid-19 symptoms from a coronavirus infection were linked to small increases in neurological, blood, and heart-related conditions in the largest global vaccine safety study to date.

    The rare events – identified early in the pandemic – included a higher risk of heart-related inflammation from mRNA shots made by Pfizer Inc, BioNTech SE, and Moderna Inc, and an increased risk of a type of blood clot in the brain after immunisation with viral-vector vaccines such as the one developed by the University of Oxford and made by AstraZeneca Plc.

    The viral-vector jabs were also tied to an increased risk of Guillain-Barre syndrome, a neurological disorder in which the immune system mistakenly attacks the peripheral nervous system.

    https://www.scmp.com/news/world/united-states-canada/article/3252387/largest-covid-19-vaccine-study-yet-finds-links-health-conditions
    Largest Covid-19 vaccine study yet finds links to health conditions Published: 12:31pm, 19 Feb, 2024 Vaccines that protect against severe illness, death and lingering long Covid-19 symptoms from a coronavirus infection were linked to small increases in neurological, blood, and heart-related conditions in the largest global vaccine safety study to date. The rare events – identified early in the pandemic – included a higher risk of heart-related inflammation from mRNA shots made by Pfizer Inc, BioNTech SE, and Moderna Inc, and an increased risk of a type of blood clot in the brain after immunisation with viral-vector vaccines such as the one developed by the University of Oxford and made by AstraZeneca Plc. The viral-vector jabs were also tied to an increased risk of Guillain-Barre syndrome, a neurological disorder in which the immune system mistakenly attacks the peripheral nervous system. https://www.scmp.com/news/world/united-states-canada/article/3252387/largest-covid-19-vaccine-study-yet-finds-links-health-conditions
    WWW.SCMP.COM
    Largest Covid-19 vaccine study yet finds links to health conditions
    More than 13.5 billion doses of Covid vaccines have been administered globally over the past three years. A small proportion were injured by the shots, stoking debate about their benefits versus harms.
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  • ⛔️Did you know that Former Pussycat Doll Jessica Sutta suffered an extreme Vaccine injury from her Moderna jab?

    You didnt did you? because CNN & BBC along with all Big Tech Social Media censored any personal testimonies detailing death & injury

    They simply didn’t want you knowing
    💊Redpilling👉 Telegram | Twitter
    ⛔️Did you know that Former Pussycat Doll Jessica Sutta suffered an extreme Vaccine injury from her Moderna jab? You didnt did you? because CNN & BBC along with all Big Tech Social Media censored any personal testimonies detailing death & injury They simply didn’t want you knowing 💊Redpilling👉 Telegram | Twitter
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  • Hydrogels in COVID Vaccine as Programmable Human Interface

    From Ana Maria Mihalcea’s "Hydrogel Platform Enables Versatile Data Encryption And Decryption"

    Greg ReeseFeb 16
    The following report is from Doctor Ana Maria Mihalcea’s recent article entitled, "Hydrogel Platform Enables Versatile Data Encryption And Decryption"

    The building blocks of Hydrogels are being found in the COVID vaccine, and Hydrogels are being found in the blood of both the vaccinated and the unvaccinated. They are the so-called blood clots that are being found around the world. And these Hydrogels can now be programmed, encrypted and decrypted. According to Mihalcea, they are the substrate of the brain computer interface and the primary method of fusing humans with machines as she described by referencing MIT research in the article, “Hydrogel Interfaces for Merging Humans and Machines”

    Elements which Mihalcea and Clifford Carnicom found with Near Infrared spectroscopy in the blood of the unvaccinated exposed to shedding and environmental contamination include hydrogel plastics such as polyenes, vinyl, nylon, kevlar, and spider silk proteins. As well as other nanotechnology signatures such as silicone and sulfur. This technology hijacks methyl groups, which are needed to detoxify and create Glutathione in the body. Hydrogels used for the encrypted programmable technology include polyvinyl alcohol and polycaprolacton. Both of these Hydrogels are listed as stealth nanoparticles in the Moderna patent for lipid nanoparticle composition. This suggests that not only those who received the shot have this hydrogel encryption technology in their bodies, but also those who have experienced shedding and environmental contamination. Which is just about everyone.

    These hydrogels are known to be programmable and encrypted. This technology can behave as brain storage. It can store memories and visual information in an individual’s brain. And it can be chemical-induced to be securely encrypted and decrypted allowing for the secure recording and storage of confidential visual information. This provides a platform for secure financial transactions, which is a requirement for a digital ID.

    MIT researchers have discussed how this very same technology can be used to fuse humans with machines. And while they’ve had problems working it out in the past, a recent paper has announced they’ve found success using the very same elements found in both the blood of the vaccinated and unvaccinated by Mihalcea and Carnicom.

    In a lecture by Professor Sakhrat Khizroev at the University of Miami, it is discussed how advanced materials can be used for interfacing machines and the human brain. He references a research project funded by DARPA wherein magnetic nanoparticles are key to this technology. Mihalcea has published research that shows how the COVID shots alter torsion fields in the body and produce magnetism. A review by the Rand Corporation, “Brain Computer Interfaces: US Military Applications and Implications” discusses the convergence of human with machine.

    In an interview with Big Pharma whistleblower, Karen Kingston, Kingston discusses this self assembly nanotechnology and how the spike protein is an engineered device, triggered by electromagnetic frequency, and how the Quantum Dots are gene editing technology. This nanotechnology appears to be distributed via Chemtrails, the food and water supply, medications, and in all of the scheduled vaccines for children. It has been found by multiple scientists in the blood of both the vaccinated and the unvaccinated. And the fact that this widespread technology is being ignored while the topic of mRNA is being pushed into the mainstream, is of great concern.

    Mihalcea has shown that the new protocols being sold to the public as a way of reversing the negative effects of the COVID shots, have no effect on these Hydrogels. And it would seem that well over a billion people are infected with them.

    While many are talking about an archaic implanted computer chip, it seems that the latest breakthrough technology has already been deployed without anyone’s consent.

    The situation almost seems hopeless, but where there is a will there is a way. And now is not the time to hide our head in the sand. The human body is miraculous and our potential is endless. The more people addressing this dire situation, the better chances we have of finding a remedy.

    https://rumble.com/v4dqd6t-hydrogels-in-covid-vaccine-as-programmable-human-interface.html
    Hydrogels in COVID Vaccine as Programmable Human Interface From Ana Maria Mihalcea’s "Hydrogel Platform Enables Versatile Data Encryption And Decryption" Greg ReeseFeb 16 The following report is from Doctor Ana Maria Mihalcea’s recent article entitled, "Hydrogel Platform Enables Versatile Data Encryption And Decryption" The building blocks of Hydrogels are being found in the COVID vaccine, and Hydrogels are being found in the blood of both the vaccinated and the unvaccinated. They are the so-called blood clots that are being found around the world. And these Hydrogels can now be programmed, encrypted and decrypted. According to Mihalcea, they are the substrate of the brain computer interface and the primary method of fusing humans with machines as she described by referencing MIT research in the article, “Hydrogel Interfaces for Merging Humans and Machines” Elements which Mihalcea and Clifford Carnicom found with Near Infrared spectroscopy in the blood of the unvaccinated exposed to shedding and environmental contamination include hydrogel plastics such as polyenes, vinyl, nylon, kevlar, and spider silk proteins. As well as other nanotechnology signatures such as silicone and sulfur. This technology hijacks methyl groups, which are needed to detoxify and create Glutathione in the body. Hydrogels used for the encrypted programmable technology include polyvinyl alcohol and polycaprolacton. Both of these Hydrogels are listed as stealth nanoparticles in the Moderna patent for lipid nanoparticle composition. This suggests that not only those who received the shot have this hydrogel encryption technology in their bodies, but also those who have experienced shedding and environmental contamination. Which is just about everyone. These hydrogels are known to be programmable and encrypted. This technology can behave as brain storage. It can store memories and visual information in an individual’s brain. And it can be chemical-induced to be securely encrypted and decrypted allowing for the secure recording and storage of confidential visual information. This provides a platform for secure financial transactions, which is a requirement for a digital ID. MIT researchers have discussed how this very same technology can be used to fuse humans with machines. And while they’ve had problems working it out in the past, a recent paper has announced they’ve found success using the very same elements found in both the blood of the vaccinated and unvaccinated by Mihalcea and Carnicom. In a lecture by Professor Sakhrat Khizroev at the University of Miami, it is discussed how advanced materials can be used for interfacing machines and the human brain. He references a research project funded by DARPA wherein magnetic nanoparticles are key to this technology. Mihalcea has published research that shows how the COVID shots alter torsion fields in the body and produce magnetism. A review by the Rand Corporation, “Brain Computer Interfaces: US Military Applications and Implications” discusses the convergence of human with machine. In an interview with Big Pharma whistleblower, Karen Kingston, Kingston discusses this self assembly nanotechnology and how the spike protein is an engineered device, triggered by electromagnetic frequency, and how the Quantum Dots are gene editing technology. This nanotechnology appears to be distributed via Chemtrails, the food and water supply, medications, and in all of the scheduled vaccines for children. It has been found by multiple scientists in the blood of both the vaccinated and the unvaccinated. And the fact that this widespread technology is being ignored while the topic of mRNA is being pushed into the mainstream, is of great concern. Mihalcea has shown that the new protocols being sold to the public as a way of reversing the negative effects of the COVID shots, have no effect on these Hydrogels. And it would seem that well over a billion people are infected with them. While many are talking about an archaic implanted computer chip, it seems that the latest breakthrough technology has already been deployed without anyone’s consent. The situation almost seems hopeless, but where there is a will there is a way. And now is not the time to hide our head in the sand. The human body is miraculous and our potential is endless. The more people addressing this dire situation, the better chances we have of finding a remedy. https://rumble.com/v4dqd6t-hydrogels-in-covid-vaccine-as-programmable-human-interface.html
    0 Comments 0 Shares 4311 Views
  • There's also a ton of information from the IEC regarding international Standards surrounding Biodigital convergence.

    Quantum Dots are programmable graphene oxide nanoparticles which serve many functions, including biometric data harvesting (spying).

    The demons want to build their Smart Cities from this material!

    https://ambassadorlove.blog/2021/12/17/quantum-dots-dna-barcoding-nano-razors-the-israeli-state/


    Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State
    December 17, 2021 by Dr. Ariyana Love
    December 2, 2021
    By Dr. Ariyana Love, ND

    In my latest interview with Stew Peter’s, I brought evidence confirming that Dr. Andreas Noack, the good doctor who risked his life to warn humanity of the extreme dangers of the death jab, is in fact deceased.

    Days after Dr. Noack’s mysterious death, a video was leaked revealing Graphene Hydroxide nano-razors inside the Pfizer death jab, under Dark Field Microscopy. The sample is loaded with Graphene Hydroxide.

    You will see an individual Microsphere releasing it’s payload of nanoscale Graphene Hydroxide which looks exactly like razorblades when zoomed in on the individual shiny specs. See more images here.

    LEAKED FOOTAGE: GRAPHENE HYDROXIDE NANO-RAZORBLADES – DARK FIELD MICROSCOPY

    An English translation of this video can be found in the article entitled, Dr. Ariyana Discusses Nano-Biosensors/Nanorazors and Dr. Noack’s Death After He Located Graphene Hydroxide in the COVID Vaccine.

    MICROSPHERES & MICROBUBBLES

    Microbeads and Microspheres are listed as an active ingredient in the Pfizer death jab patent. Microspheres and Microbubbles are listed in the Moderna death jab patent.

    Microspheres and Microbubbles are micrometer size devices approximately equal in size to a red blood cell, according to the NIH. That’s about the width of a Human hair.


    Microbubbles and Microspheres (bottom right)
    Microspheres and Microbubbles are made from Poly(lactic-co-glycolic) acid (PLGA). PLGA is a copolymer made from Graphene Oxide (GO). Graphene Oxide-PLGA nanofibers are used in a host of Food and Drug Administration (FDA) approved “therapeutic” devices. However, the ingredients of these devices are cytotoxic, meaning they destroy cells.

    Graphene Oxide PLGA Toxicity induces an inflammatory response and deadly cytokine storm reaction, according to animal studies. The FDA should be investigated for this.

    Microspheres are coated with gold nanoparticles. Microspheres are used for scaffolding, which is artificial tissue engineering inside the Human body. PubMed writes, “Scaffolds are materials that have been engineered to cause desirable cellular interactions to contribute to the formation of new functional tissues for medical purposes. Cells are often ‘seeded’ into these structures capable of supporting three-dimensional tissue formation.”

    This technology is being used for DNA-based tissue engineering and “scaffolding” of Humans, without their Informed Consent. See more scaffolding images from a Slovakian study of the death jab, here.

    Microbubbles contain one or more “viral vectors coding CRISPR-Cas-9 system“. It’s a “state-of-the-art” drug and chemical delivery method. They contain lab enhanced chimeric proteins of the messenger RNA/DNA. Microbubbles have a lipid and nickel-coated quartz substrate. They contain a drug and chemical payload in the outer, lipid-coating and another payload on the inside.

    Graphene Oxide Nanotubes enable Microbubbles to self-replicate via electrical pulse. They interlink by electrodes. Microbubbles were designed to break through the blood/brain barrier and deliver their drug and chemical payload into brain cells. Ultrasound is used to help Microbubbles breach the blood/brain barrier. Here’s a video animation of how microbubbles / microspheres work to deliver drugs into the brain.

    This gene delivery technology was funded and developed for the purpose of treating sick people, not healthy people. It was intended to be used as a treatment for cancer, not as a medical intervention for our healthy kids.

    The Microbubble and Microsphere devices carry drug and chemical payloads for controlled release of encapsulated DNA. It’s targeted drug delivery can be unloaded over an extended period of time. This is very important to understand. They can be formulated for “sustained release” and programmed to release it’s payload at a later date, over a period of days, weeks, months or years, as the Moderna patent specifies.


    Moderna patent US10703789B2 delayed drug release
    QUANTOM DOTS & MICROBEADS

    Atomic scale nanometer devices called Quantum Dots and Microbeads, are also components of the death jab weapons system. They are found in the Pfizer and Moderna patents.

    These nanoscale technological devices are 1000 times smaller than a micrometer. Quantum Dots have nothing to do with plastic particles, these are carbon based nanocrystals, 10-50 atoms thick, and made from Graphene.

    Quantom Dots are used for DNA barcoding of Humans using CRISPR-Cas-9 technology. They are super conductors made for bio-imaging and bio-tracking of Humans. They too were developed for “therapeutic” use, to eradicate cancers, not to enslave Humans.

    Quantum Dots are artificial, color based, bioluminescent marker genes. They use three colors taken from the enzymatic proteins of insects (Luciferase), glow worms and jellyfish. The chimeric proteins are being barcoded onto Human genes to make them trackable, programmable and encoded, so Human cells will light up, enabling the NWO oligarchs to monitor your every move.

    I discussed Quantum Dots and more with Stew Peters on December 9th, 2021.

    Dr. Ariyana Love on Stew Peters Show, Dec. 9, 2021
    Microbead patent US20110017493A1, verifies that Microbeads “carbon based” (made from Graphene) and Microbead patent ES2784361T3/en specifies that it’s used to create molecular barcodes in Humans.

    Thermo Ficher sells Microbeads and markets them as Dynabeads and SPIONs. See SPIONS here.

    THE ISRAELI STATE

    This technology was developed at the Hebrew University in occupied Jerusalem. The Quantum Dot patent WO201413562A1 is owned by Yissum, a Hebrew University company owned by the Israeli state and co-owned by Nanosys, a Silicon Valley based company. These two companies are sublicensing the technology, worldwide.

    Yissum business partners include Google, Intel, Johnson & Johnson, Merck, Microsoft, and many more, while Samsung has a partnership with Nanosys.

    Moderna’s patents are owned by Israel. Pfizer patents are owned by Israel. Pfizer CEO is in bed with Israel. Moderna is partnered with Israel in medical maleficence.

    Moderna’s CEO Stephane Bancel, wants every man, women and child injected with Moderna’s poison #DeathJab, including INFANTS!


    Is it clear to you now who it is that has the greatest vested interest in branding and enslaving Humans like cattle? The cloning of insect DNA (Luciferase) into Humans is called cross-species genomics. This is the process of manually adding DNA from insects into Humans by transfection, a process also known as cloning, in order to change the genetic makeup of cells. It works by deleting one or more gene from the Human host and encodes Human cells to express the new genetic trait of an insect. Is that what you want to become?


    BIOCHIP & HYDROGEL

    Dr. Pablo Campra mentioned that nano-biosensors are in the death jabs. They can be found in the DARPA patent US7427497B2/en which lists “T-shaped micro-fluidic Biochips”.


    Hydrogels contain the entire mRNA weapons system. They need us saturated with their cloning technology in order to succeed in genetically modifying Humans to the point of patent eligibility. They will do so by injections, masks, nasal swabs, hand sanitizer, aerial spraying, and any other means necessary to achieve their end goal.

    We are in fact being saturated with Graphene Oxide Hydrogels. They’re being inserted into our food, clothing, hair and make-up products, household cleaners, alcohol, pharmaceutical drugs, sanitary items, water supply, etc.

    Ethylene Oxide in masks and on PCR swabs, is in fact Graphene Oxide, Poly(ethylene oxide) Graphene Nanoribbons. The bad news is that Fauci and the NIH funded mRNA nanotechnology which is skin-penetrating and can be dispensed via aerial spraying, as reported by InfoWars. The good news is this weapons system can also be expelled through the skin, if you know how to properly detox. The key to protecting yourself from this biological attack is to boost your immune system and remain on a continued Protocol.

    PROTOCOL

    There is a special natural supplement that disables the operating system, kills the parasites, and removes Graphene and other metals, effectively expelling them from your body. This supplement increases endogenous glutathione by 800%, repairs damage to your cells and to your DNA, and turns genes on, according to scientific research. This medical breakthrough is being used now by doctors who are able to reverse the coagulation cascade in just minutes. You will find this supplement in my Protocol here.

    https://donshafi911.blogspot.com/2024/02/quantum-dots-dna-barcoding-nano-razors.html
    There's also a ton of information from the IEC regarding international Standards surrounding Biodigital convergence. Quantum Dots are programmable graphene oxide nanoparticles which serve many functions, including biometric data harvesting (spying). The demons want to build their Smart Cities from this material! https://ambassadorlove.blog/2021/12/17/quantum-dots-dna-barcoding-nano-razors-the-israeli-state/ Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State December 17, 2021 by Dr. Ariyana Love December 2, 2021 By Dr. Ariyana Love, ND In my latest interview with Stew Peter’s, I brought evidence confirming that Dr. Andreas Noack, the good doctor who risked his life to warn humanity of the extreme dangers of the death jab, is in fact deceased. Days after Dr. Noack’s mysterious death, a video was leaked revealing Graphene Hydroxide nano-razors inside the Pfizer death jab, under Dark Field Microscopy. The sample is loaded with Graphene Hydroxide. You will see an individual Microsphere releasing it’s payload of nanoscale Graphene Hydroxide which looks exactly like razorblades when zoomed in on the individual shiny specs. See more images here. LEAKED FOOTAGE: GRAPHENE HYDROXIDE NANO-RAZORBLADES – DARK FIELD MICROSCOPY An English translation of this video can be found in the article entitled, Dr. Ariyana Discusses Nano-Biosensors/Nanorazors and Dr. Noack’s Death After He Located Graphene Hydroxide in the COVID Vaccine. MICROSPHERES & MICROBUBBLES Microbeads and Microspheres are listed as an active ingredient in the Pfizer death jab patent. Microspheres and Microbubbles are listed in the Moderna death jab patent. Microspheres and Microbubbles are micrometer size devices approximately equal in size to a red blood cell, according to the NIH. That’s about the width of a Human hair. Microbubbles and Microspheres (bottom right) Microspheres and Microbubbles are made from Poly(lactic-co-glycolic) acid (PLGA). PLGA is a copolymer made from Graphene Oxide (GO). Graphene Oxide-PLGA nanofibers are used in a host of Food and Drug Administration (FDA) approved “therapeutic” devices. However, the ingredients of these devices are cytotoxic, meaning they destroy cells. Graphene Oxide PLGA Toxicity induces an inflammatory response and deadly cytokine storm reaction, according to animal studies. The FDA should be investigated for this. Microspheres are coated with gold nanoparticles. Microspheres are used for scaffolding, which is artificial tissue engineering inside the Human body. PubMed writes, “Scaffolds are materials that have been engineered to cause desirable cellular interactions to contribute to the formation of new functional tissues for medical purposes. Cells are often ‘seeded’ into these structures capable of supporting three-dimensional tissue formation.” This technology is being used for DNA-based tissue engineering and “scaffolding” of Humans, without their Informed Consent. See more scaffolding images from a Slovakian study of the death jab, here. Microbubbles contain one or more “viral vectors coding CRISPR-Cas-9 system“. It’s a “state-of-the-art” drug and chemical delivery method. They contain lab enhanced chimeric proteins of the messenger RNA/DNA. Microbubbles have a lipid and nickel-coated quartz substrate. They contain a drug and chemical payload in the outer, lipid-coating and another payload on the inside. Graphene Oxide Nanotubes enable Microbubbles to self-replicate via electrical pulse. They interlink by electrodes. Microbubbles were designed to break through the blood/brain barrier and deliver their drug and chemical payload into brain cells. Ultrasound is used to help Microbubbles breach the blood/brain barrier. Here’s a video animation of how microbubbles / microspheres work to deliver drugs into the brain. This gene delivery technology was funded and developed for the purpose of treating sick people, not healthy people. It was intended to be used as a treatment for cancer, not as a medical intervention for our healthy kids. The Microbubble and Microsphere devices carry drug and chemical payloads for controlled release of encapsulated DNA. It’s targeted drug delivery can be unloaded over an extended period of time. This is very important to understand. They can be formulated for “sustained release” and programmed to release it’s payload at a later date, over a period of days, weeks, months or years, as the Moderna patent specifies. Moderna patent US10703789B2 delayed drug release QUANTOM DOTS & MICROBEADS Atomic scale nanometer devices called Quantum Dots and Microbeads, are also components of the death jab weapons system. They are found in the Pfizer and Moderna patents. These nanoscale technological devices are 1000 times smaller than a micrometer. Quantum Dots have nothing to do with plastic particles, these are carbon based nanocrystals, 10-50 atoms thick, and made from Graphene. Quantom Dots are used for DNA barcoding of Humans using CRISPR-Cas-9 technology. They are super conductors made for bio-imaging and bio-tracking of Humans. They too were developed for “therapeutic” use, to eradicate cancers, not to enslave Humans. Quantum Dots are artificial, color based, bioluminescent marker genes. They use three colors taken from the enzymatic proteins of insects (Luciferase), glow worms and jellyfish. The chimeric proteins are being barcoded onto Human genes to make them trackable, programmable and encoded, so Human cells will light up, enabling the NWO oligarchs to monitor your every move. I discussed Quantum Dots and more with Stew Peters on December 9th, 2021. Dr. Ariyana Love on Stew Peters Show, Dec. 9, 2021 Microbead patent US20110017493A1, verifies that Microbeads “carbon based” (made from Graphene) and Microbead patent ES2784361T3/en specifies that it’s used to create molecular barcodes in Humans. Thermo Ficher sells Microbeads and markets them as Dynabeads and SPIONs. See SPIONS here. THE ISRAELI STATE This technology was developed at the Hebrew University in occupied Jerusalem. The Quantum Dot patent WO201413562A1 is owned by Yissum, a Hebrew University company owned by the Israeli state and co-owned by Nanosys, a Silicon Valley based company. These two companies are sublicensing the technology, worldwide. Yissum business partners include Google, Intel, Johnson & Johnson, Merck, Microsoft, and many more, while Samsung has a partnership with Nanosys. Moderna’s patents are owned by Israel. Pfizer patents are owned by Israel. Pfizer CEO is in bed with Israel. Moderna is partnered with Israel in medical maleficence. Moderna’s CEO Stephane Bancel, wants every man, women and child injected with Moderna’s poison #DeathJab, including INFANTS! Is it clear to you now who it is that has the greatest vested interest in branding and enslaving Humans like cattle? The cloning of insect DNA (Luciferase) into Humans is called cross-species genomics. This is the process of manually adding DNA from insects into Humans by transfection, a process also known as cloning, in order to change the genetic makeup of cells. It works by deleting one or more gene from the Human host and encodes Human cells to express the new genetic trait of an insect. Is that what you want to become? BIOCHIP & HYDROGEL Dr. Pablo Campra mentioned that nano-biosensors are in the death jabs. They can be found in the DARPA patent US7427497B2/en which lists “T-shaped micro-fluidic Biochips”. Hydrogels contain the entire mRNA weapons system. They need us saturated with their cloning technology in order to succeed in genetically modifying Humans to the point of patent eligibility. They will do so by injections, masks, nasal swabs, hand sanitizer, aerial spraying, and any other means necessary to achieve their end goal. We are in fact being saturated with Graphene Oxide Hydrogels. They’re being inserted into our food, clothing, hair and make-up products, household cleaners, alcohol, pharmaceutical drugs, sanitary items, water supply, etc. Ethylene Oxide in masks and on PCR swabs, is in fact Graphene Oxide, Poly(ethylene oxide) Graphene Nanoribbons. The bad news is that Fauci and the NIH funded mRNA nanotechnology which is skin-penetrating and can be dispensed via aerial spraying, as reported by InfoWars. The good news is this weapons system can also be expelled through the skin, if you know how to properly detox. The key to protecting yourself from this biological attack is to boost your immune system and remain on a continued Protocol. PROTOCOL There is a special natural supplement that disables the operating system, kills the parasites, and removes Graphene and other metals, effectively expelling them from your body. This supplement increases endogenous glutathione by 800%, repairs damage to your cells and to your DNA, and turns genes on, according to scientific research. This medical breakthrough is being used now by doctors who are able to reverse the coagulation cascade in just minutes. You will find this supplement in my Protocol here. https://donshafi911.blogspot.com/2024/02/quantum-dots-dna-barcoding-nano-razors.html
    0 Comments 0 Shares 8217 Views
  • 🚨 Moderna is Planning Another COVID Campaign Starting April 2025

    💉The COVID-19 vaccine industry is in trouble, with Big Pharma players such as Pfizer and Moderna undergoing significant turbulence. The departure of key sales executives further exacerbates the challenges faced by these companies.

    Endpoints News reports: "[Moderna] reaffirmed its focus on driving Covid-19 and soon RSV vaccine sales, though the former’s sales have been challenged by waning demand. Moderna said last month that it expects Covid sales to “hit a low point” in 2024, while Pfizer recently slashed expectations for its Comirnaty shot by $2 billion."

    "Pfizer also announced an executive shake-up on Tuesday. Chief commercial officer and global biopharma president Angela Hwang will depart after 27 years at the pharma giant as the company creates two non-oncology commercial units.

    …the company prepares to launch its RSV vaccine in 2024 and promises to deliver “multiple products per year from 2025 forward.” The company stuck to its full-year 2023 sales guidance of $6 billion to $8 billion on its latest quarterly call, but said the low end is more realistic, also noting a $1.3 billion write-down for “excess and obsolete” Covid product. Executives expect 2024 revenue to be around $4 billion."

    "However, according to my secret sources, it appears that after an anticipated “low point” in 2024, Moderna expects that covid vaccine volume will steeply ramp up again starting in April 2025. According to an insider (don’t ask me how I got this): Moderna is preparing to launch 15 mRNA products in the next 5 years. Up to four of those could come by 2025," revealed Sasha Latypova, a former pharmaceutical industry executive with 25 years experience in various roles. Her clients included Pfizer, Johnson & Johnson, Novartis, AstraZeneca, GSK, and more.

    Full story: 👇
    https://sashalatypova.substack.com/p/future-outlook-moderna-is-planning

    Join ➡️ @ShankaraChetty


    Moderna is planning another covid campaign starting April 2025.
    Employees are asked to donate blood for experiments in exchange for $75 gift cards.

    Sasha Latypova
    According to Endpoints News, covid vax business is in trouble - both Pfizer and Moderna are tanking, and heads of sales have departed:

    [Moderna] reaffirmed its focus on driving Covid-19 and soon RSV vaccine sales, though the former’s sales have been challenged by waning demand. Moderna said last month that it expects Covid sales to “hit a low point” in 2024, while Pfizer recently slashed expectations for its Comirnaty shot by $2 billion.

    Pfizer also announced an executive shake-up on Tuesday. Chief commercial officer and global biopharma president Angela Hwang will depart after 27 years at the pharma giant as the company creates two non-oncology commercial units.

    …the company prepares to launch its RSV vaccine in 2024 and promises to deliver “multiple products per year from 2025 forward.” The company stuck to its full-year 2023 sales guidance of $6 billion to $8 billion on its latest quarterly call, but said the low end is more realistic, also noting a $1.3 billion write-down for “excess and obsolete” Covid product. Executives expect 2024 revenue to be around $4 billion.

    However, according to my secret sources, it appears that after an anticipated “low point” in 2024, Moderna expects that covid vaccine volume will steeply ramp up again starting in April 2025.

    According to an insider (don’t ask me how I got this):

    Moderna is preparing to launch 15 mRNA products in the next 5 years. Up to four of those could come by 2025.

    Review of Moderna’s publicly available full of shit R&D pipeline indicates that indeed, there are 4-5 different mRNA vaxxes for flu in late stages of development, another one for RSV, then different combos of flu-Covid+RSV, etc.

    Also, looks like gene therapies have been renamed into “intracellular therapeutics”. Gosh, all that attention to gene hacking is not great for PR! They still sport old failures like the CMV and zika vaxxes, on their pipeline, including the gene therapy (ahem, intracellular therapeutic) for Crigler-Najar syndrome which conclusively failed around 2012, that’s eons ago! They are claiming they gave it away for free to something called The Institute for Life Changing Medicines. It’s life changing, for sure… the founder of this Institute, Tachi Yamada “passed away unexpectedly” in August 2021. I wonder what was the cause of death? He looked not old and quite healthy… Maybe he partook in the intracellular miracles?

    More from my secret Moderna source:

    There is an email today asking for employees to donate blood to develop assays that will be used to generate key data in their clinical trials. They are offering $75 gift cards.

    Starting April of 2025 the covid campaign [is expected to] kick off, [therefore] by April of 2024 they will be in full covid vax production.

    I find it odd this year [2023] there was no covid vax production, boosters etc were basically left over from the original product runs.

    I am going to speculate here about this interesting timing:

    2024 is an election year! Biden (or a suitable puppet substitute) needs to be installed/reinstalled, and therefore the government’s covid boot should be off our necks since it is associated too much with the current regime. The authorized “freedom” narrative goes like this: Mistakes were made, dolts botched shit, replace those dolts with some other dolts, do some listening sessions to pretend public pushback had some impact. Do some bombshell interviews on Tucker Carlson’s show, where literal truth bombs like “Pfizer lied!!” “FDA didn’t do its job!” and “WHO bad!” are allowed to be dropped. Blame Pfizer for everything! (don’t mention Moderna too often, best - not at all). Even allow somebody to sue Pfizer! Blame the corporate greed, the greedy capitalists, corporations and stuff. Note: the federal government is not at fault, they are saintly incompetent people prone to making many mistakes. They are sincerely stupid, and just can’t see the data! Ask them to look at the VAERS data one more time…

    There is non-zero probability that Pfizer production may be shut down at some point: maybe FDA will “find” manufacturing violations, or maybe AG Paxton will miraculously prevail in his lawsuit in TX for false advertising, maybe investigation by Ron DeSantis will miraculously turn out not to be a fake political stunt - there are several potential scenarios how this will unfold. Note, this post was written and scheduled several weeks ago. Late breaking news: Ron DeSantis’s grand jury is a political stunt and a total joke. In any case, Moderna might become the “exclusive” manufacturer of Poison-19, just like Emergent Biosolutions is exclusive for the anthrax poisoning-of-the-troops elixir. Hence, planning ramped up volumes in 2025.

    Since Moderna is a DOD/DARPA/CDC/CIA company, this should tell us that the government are planning another bunch of false flags, fear mongering and generation of “sentinel cases” (cruise ships, Navy ships, subways, large events, other crowded places) for some “new mutated covid variant” in 2025. Or they are simply expecting the VAIDS to ramp up by 2025. Or all/combinations of the above.

    It should be noted that Moderna doesn’t really make their product, it is made for them by the DOD/CIA’s baby Resilience - a biomanufacturing behemoth, funded and controlled by the federal government. Resilience goes by several names (aka Nanotherapeutics, Ology and a few others), and has many strong links to the CIA and Inqtel (CIA’s “venture fund”). Here is a well made 7 min analysis, click on the link:

    https://twitter.com/Cancelcloco/status/1735421884395860246


    Here is my prediction for the dominant narratives in regard to this for the elections year - R vs D affiliations do not matter. Only the candidates that are beholden to the Pandemic Preparedness Cult (here, here, here) will be allowed to proceed to the actual ticket. So that the DOD/CIA control them no matter what the outcome of the elections. It is crucial for the DOD/CIA to continue making poison, pumping poison and profit from it. Thus, be prepared for your favorite candidate to endorse the idea of pandemics and outbreaks of dangerous pathogens, the idea that the government must “protect” us from these dangers, the stories of dolts botching shit, pointing of fingers at their opponent who was “pro-lockdown and masking”, promises to replace dolts with some other better dolts, even promises to get Pfizer and their corporate greed “brought to justice”, sort of. But do not expect any of your favorite candidates to point at the root cause of the millions of dead and injured - the federal government and its goon agents who built the illegal-legal cage where genocide is completely legal, or at a minimum, impossible to prosecute. That’s because the goal of your favorite political candidate is to align with the interests of that awesome federal government power pyramid in order to be hired as its next sock puppet, not to upset or reform it.

    Art for today: Hydrangea and Sake Bottle, oil on panel, 14x18 in.

    https://donshafi911.blogspot.com/2024/02/moderna-is-planning-another-covid.html

    🚨 Moderna is Planning Another COVID Campaign Starting April 2025 💉The COVID-19 vaccine industry is in trouble, with Big Pharma players such as Pfizer and Moderna undergoing significant turbulence. The departure of key sales executives further exacerbates the challenges faced by these companies. Endpoints News reports: "[Moderna] reaffirmed its focus on driving Covid-19 and soon RSV vaccine sales, though the former’s sales have been challenged by waning demand. Moderna said last month that it expects Covid sales to “hit a low point” in 2024, while Pfizer recently slashed expectations for its Comirnaty shot by $2 billion." "Pfizer also announced an executive shake-up on Tuesday. Chief commercial officer and global biopharma president Angela Hwang will depart after 27 years at the pharma giant as the company creates two non-oncology commercial units. …the company prepares to launch its RSV vaccine in 2024 and promises to deliver “multiple products per year from 2025 forward.” The company stuck to its full-year 2023 sales guidance of $6 billion to $8 billion on its latest quarterly call, but said the low end is more realistic, also noting a $1.3 billion write-down for “excess and obsolete” Covid product. Executives expect 2024 revenue to be around $4 billion." "However, according to my secret sources, it appears that after an anticipated “low point” in 2024, Moderna expects that covid vaccine volume will steeply ramp up again starting in April 2025. According to an insider (don’t ask me how I got this): Moderna is preparing to launch 15 mRNA products in the next 5 years. Up to four of those could come by 2025," revealed Sasha Latypova, a former pharmaceutical industry executive with 25 years experience in various roles. Her clients included Pfizer, Johnson & Johnson, Novartis, AstraZeneca, GSK, and more. Full story: 👇 https://sashalatypova.substack.com/p/future-outlook-moderna-is-planning Join ➡️ @ShankaraChetty Moderna is planning another covid campaign starting April 2025. Employees are asked to donate blood for experiments in exchange for $75 gift cards. Sasha Latypova According to Endpoints News, covid vax business is in trouble - both Pfizer and Moderna are tanking, and heads of sales have departed: [Moderna] reaffirmed its focus on driving Covid-19 and soon RSV vaccine sales, though the former’s sales have been challenged by waning demand. Moderna said last month that it expects Covid sales to “hit a low point” in 2024, while Pfizer recently slashed expectations for its Comirnaty shot by $2 billion. Pfizer also announced an executive shake-up on Tuesday. Chief commercial officer and global biopharma president Angela Hwang will depart after 27 years at the pharma giant as the company creates two non-oncology commercial units. …the company prepares to launch its RSV vaccine in 2024 and promises to deliver “multiple products per year from 2025 forward.” The company stuck to its full-year 2023 sales guidance of $6 billion to $8 billion on its latest quarterly call, but said the low end is more realistic, also noting a $1.3 billion write-down for “excess and obsolete” Covid product. Executives expect 2024 revenue to be around $4 billion. However, according to my secret sources, it appears that after an anticipated “low point” in 2024, Moderna expects that covid vaccine volume will steeply ramp up again starting in April 2025. According to an insider (don’t ask me how I got this): Moderna is preparing to launch 15 mRNA products in the next 5 years. Up to four of those could come by 2025. Review of Moderna’s publicly available full of shit R&D pipeline indicates that indeed, there are 4-5 different mRNA vaxxes for flu in late stages of development, another one for RSV, then different combos of flu-Covid+RSV, etc. Also, looks like gene therapies have been renamed into “intracellular therapeutics”. Gosh, all that attention to gene hacking is not great for PR! They still sport old failures like the CMV and zika vaxxes, on their pipeline, including the gene therapy (ahem, intracellular therapeutic) for Crigler-Najar syndrome which conclusively failed around 2012, that’s eons ago! They are claiming they gave it away for free to something called The Institute for Life Changing Medicines. It’s life changing, for sure… the founder of this Institute, Tachi Yamada “passed away unexpectedly” in August 2021. I wonder what was the cause of death? He looked not old and quite healthy… Maybe he partook in the intracellular miracles? More from my secret Moderna source: There is an email today asking for employees to donate blood to develop assays that will be used to generate key data in their clinical trials. They are offering $75 gift cards. Starting April of 2025 the covid campaign [is expected to] kick off, [therefore] by April of 2024 they will be in full covid vax production. I find it odd this year [2023] there was no covid vax production, boosters etc were basically left over from the original product runs. I am going to speculate here about this interesting timing: 2024 is an election year! Biden (or a suitable puppet substitute) needs to be installed/reinstalled, and therefore the government’s covid boot should be off our necks since it is associated too much with the current regime. The authorized “freedom” narrative goes like this: Mistakes were made, dolts botched shit, replace those dolts with some other dolts, do some listening sessions to pretend public pushback had some impact. Do some bombshell interviews on Tucker Carlson’s show, where literal truth bombs like “Pfizer lied!!” “FDA didn’t do its job!” and “WHO bad!” are allowed to be dropped. Blame Pfizer for everything! (don’t mention Moderna too often, best - not at all). Even allow somebody to sue Pfizer! Blame the corporate greed, the greedy capitalists, corporations and stuff. Note: the federal government is not at fault, they are saintly incompetent people prone to making many mistakes. They are sincerely stupid, and just can’t see the data! Ask them to look at the VAERS data one more time… There is non-zero probability that Pfizer production may be shut down at some point: maybe FDA will “find” manufacturing violations, or maybe AG Paxton will miraculously prevail in his lawsuit in TX for false advertising, maybe investigation by Ron DeSantis will miraculously turn out not to be a fake political stunt - there are several potential scenarios how this will unfold. Note, this post was written and scheduled several weeks ago. Late breaking news: Ron DeSantis’s grand jury is a political stunt and a total joke. In any case, Moderna might become the “exclusive” manufacturer of Poison-19, just like Emergent Biosolutions is exclusive for the anthrax poisoning-of-the-troops elixir. Hence, planning ramped up volumes in 2025. Since Moderna is a DOD/DARPA/CDC/CIA company, this should tell us that the government are planning another bunch of false flags, fear mongering and generation of “sentinel cases” (cruise ships, Navy ships, subways, large events, other crowded places) for some “new mutated covid variant” in 2025. Or they are simply expecting the VAIDS to ramp up by 2025. Or all/combinations of the above. It should be noted that Moderna doesn’t really make their product, it is made for them by the DOD/CIA’s baby Resilience - a biomanufacturing behemoth, funded and controlled by the federal government. Resilience goes by several names (aka Nanotherapeutics, Ology and a few others), and has many strong links to the CIA and Inqtel (CIA’s “venture fund”). Here is a well made 7 min analysis, click on the link: https://twitter.com/Cancelcloco/status/1735421884395860246 Here is my prediction for the dominant narratives in regard to this for the elections year - R vs D affiliations do not matter. Only the candidates that are beholden to the Pandemic Preparedness Cult (here, here, here) will be allowed to proceed to the actual ticket. So that the DOD/CIA control them no matter what the outcome of the elections. It is crucial for the DOD/CIA to continue making poison, pumping poison and profit from it. Thus, be prepared for your favorite candidate to endorse the idea of pandemics and outbreaks of dangerous pathogens, the idea that the government must “protect” us from these dangers, the stories of dolts botching shit, pointing of fingers at their opponent who was “pro-lockdown and masking”, promises to replace dolts with some other better dolts, even promises to get Pfizer and their corporate greed “brought to justice”, sort of. But do not expect any of your favorite candidates to point at the root cause of the millions of dead and injured - the federal government and its goon agents who built the illegal-legal cage where genocide is completely legal, or at a minimum, impossible to prosecute. That’s because the goal of your favorite political candidate is to align with the interests of that awesome federal government power pyramid in order to be hired as its next sock puppet, not to upset or reform it. Art for today: Hydrangea and Sake Bottle, oil on panel, 14x18 in. https://donshafi911.blogspot.com/2024/02/moderna-is-planning-another-covid.html
    SASHALATYPOVA.SUBSTACK.COM
    Moderna is planning another covid campaign starting April 2025.
    Employees are asked to donate blood for experiments in exchange for $75 gift cards.
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  • Moderna Vaccine Patented 9 Months Before Pandemic: Expert Reveals.
    www.vtforeignpolicy.com/2024/02/moderna-vaccine-questions/
    Moderna Vaccine Patented 9 Months Before Pandemic: Expert Reveals. www.vtforeignpolicy.com/2024/02/moderna-vaccine-questions/
    Moderna Vaccine Patented 9 Months Before Pandemic: Expert Reveals
    A disturbing document had already emerged proving the existence of an experimental gene serum based on messenger RNA against COVID - 19 on 12 December 2019.
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  • The COVID-19 Vaccine Antigen Is ANTHRAX
    Dr. Ariyana Love
    By Dr. Ariyana Love

    Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein.

    We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX?

    “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.”

    Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention.

    A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more.

    According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast).

    Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.”

    The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out.


    Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides


    In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”.

    Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible.

    Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects.


    PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses


    The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare.

    In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg.

    Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs.

    Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant.

    The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels.

    Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax.

    Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

    SPIKE PROTEIN IS AEROSOLIZED ANTHRAX

    There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.”

    The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”.

    “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.”

    The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions.

    The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells.

    The following quote about the Anthrax “protective antigen” is particularly revealing:

    “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).”

    Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”.

    Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized.

    This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic.

    This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality.

    ALHYDROGEL

    According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel.

    Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health.

    In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”.

    In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death.

    Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network.

    Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system.

    This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from?

    This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel.

    “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA.

    Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public.

    Alhydrogel was improved and transformed into the Nanoalum adjuvant.

    Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor.

    Alhydrogel is also carried in the lipid coating of nanoparticles.

    The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites.


    Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector!


    ANTHRAX SYMPTOMS AND TREATMENT

    Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs.

    Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance).

    Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time.


    Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review


    Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers.

    The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis?

    Anthrax also coagulates the blood.

    “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.”

    Read more here and here.

    Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax.

    It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation.


    This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia.

    All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal.

    Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen.

    Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI.

    Heroine users in Europe have been tested with Injection Anthrax.

    Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind:

    “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.”

    TREATMENT

    If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax.

    Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning.

    Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol.

    I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system.

    Please follow me on Telegram @drloveariyana and X @drloveariyana.

    If you would like to donate to my research, please do so here.


    UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE.

    The Covid-19 Vaccine Antigen Is ANTHRAX

    Read more:
    https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true


    https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
    The COVID-19 Vaccine Antigen Is ANTHRAX Dr. Ariyana Love By Dr. Ariyana Love Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX? “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.” Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention. A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more. According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast). Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.” The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out. Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects. PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare. In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg. Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant. The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels. Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax. Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero SPIKE PROTEIN IS AEROSOLIZED ANTHRAX There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.” The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”. “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.” The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions. The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells. The following quote about the Anthrax “protective antigen” is particularly revealing: “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).” Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized. This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic. This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality. ALHYDROGEL According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel. Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health. In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”. In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death. Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network. Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system. This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from? This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel. “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA. Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public. Alhydrogel was improved and transformed into the Nanoalum adjuvant. Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor. Alhydrogel is also carried in the lipid coating of nanoparticles. The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites. Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector! ANTHRAX SYMPTOMS AND TREATMENT Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs. Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance). Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time. Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers. The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis? Anthrax also coagulates the blood. “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.” Read more here and here. Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax. It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation. This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia. All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal. Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen. Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI. Heroine users in Europe have been tested with Injection Anthrax. Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind: “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.” TREATMENT If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax. Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning. Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol. I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system. Please follow me on Telegram @drloveariyana and X @drloveariyana. If you would like to donate to my research, please do so here. UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE. The Covid-19 Vaccine Antigen Is ANTHRAX Read more: https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
    Angry
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  • ED DOWD: “Safe and Effective” Is the Biggest Fraud of Our Lifetime

    “And it’s unwinding,” he says.

    “All you have to do is look at the Pfizer stock price – look at the Moderna stock price, and they are hitting new lows every day.”

    “And there’s a reason why,” Dowd added.

    “Even though the mainstream media and our medical institutions won’t admit what’s going on, the word’s gotten out and uptake of the magic juice inoculations is about 6% now.”

    @DowdEdward, @Jimmy_Dore

    https://x.com/vigilantfox/status/1753475378021072944?s=46
    ED DOWD: “Safe and Effective” Is the Biggest Fraud of Our Lifetime “And it’s unwinding,” he says. “All you have to do is look at the Pfizer stock price – look at the Moderna stock price, and they are hitting new lows every day.” “And there’s a reason why,” Dowd added. “Even though the mainstream media and our medical institutions won’t admit what’s going on, the word’s gotten out and uptake of the magic juice inoculations is about 6% now.” @DowdEdward, @Jimmy_Dore https://x.com/vigilantfox/status/1753475378021072944?s=46
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  • Japanese professor files lawsuit against Ministry of Health regarding vaccine safety and efficacy!
    John Smith
    Masanori Fukushima (福島雅典), professor emeritus at Kyoto University in Japan, has filed a lawsuit against the Japanese Ministry of Health, Labor, and Welfare (MHLW).[i]


    https://twitter.com/ShortShort_News/status/1622224704064098304 - Click image to watch a clip of the conference
    The lawsuit seeks the following:

    The disclosure of all safety and efficacy data of the covid-19 vaccines, submitted by Pfizer and Moderna to the MHLW and the PMDA (Japanese pharmaceutical and medical device regulation agency similar to the FDA)

    Full disclosure of the contracts between Japan and the pharmaceutical companies (i.e., Pfizer, Moderna, etc.)

    Compensation for those injured by the covid-19 vaccines

    Professor Fukushima has over 25 years of experience as an oncologist, and is also the Director and Chairman of the Translational Research Informatics Center in Japan, which is the first academic center in Japan dedicated to transforming basic medical research into clinical practices. He also became involved in pharmacoepidemiology (the study of interactions between drugs and human populations) since 2000.


    Professor Fukushima in a recent Japanese interview https://www.nicovideo.jp/watch/sm41745638

    Professor Fukushima is director of the TRI https://advances.tri-kobe.org/en/feature/11/from-lab-to-clinic.html
    In November 2022, Professor Fukushima had previously hosted a discussion with other doctors and professors where he condemned the Japanese MHLW for ignoring the dangers of the covid-19 vaccines. Professor Fukushima had demanded investigations into all covid-19 vaccine injuries in a thorough case by case evaluation of medical records. He also warned of the indefinite production of spike proteins via the covid-19 vaccines, as well as the side effects due to lipid nanoparticles.


    https://rumble.com/v1yofle-japanese-professor-rebukes-ministry-of-health-dissolve-vaccine-committiee-i.html
    Then in December 2022, Professor Fukushima had stated in an interview his intention to sue the Japanese government because its refusal to disclose vital information regarding the efficacy of the covid-19 vaccines.

    Which brings us to the current situation where on February 2nd 2023, Professor Fukushima held the press conference for his lawsuit at the Tokyo District Court.

    In addition to the lawsuit demands previously mentioned, he also warned that additional lawsuits may be filed if the Japanese MHLW does not acknowledge a causal link between the vaccine and their associated deaths.

    Professor Fukushima skeptically questions the actual result of the 90 trillion yen spent by the government on the covid-19 vaccines. Speaking not only as a doctor and scientist, but also as a citizen and taxpayer, he sees it as part of his duty on behalf of the nation to understand the real effect of the vaccines. He believes surprising information will be revealed from the disclosure of the documents from the pharmaceutical manufacturing companies. He is also studying the pathological mechanisms of the vaccines with other experts as well as medical guidelines for the treatment of vaccine injuries.[ii]

    Japanese law already stipulates compensation for the vaccine injured, so Professor Fukushima argues that it should be applied now. The Japanese vaccination law outlines the scope of benefits as follows (computer translation from their website):


    https://elaws.e-gov.go.jp/document?lawid=323AC0000000068
    Below is a transcript of a clip of the February 2023 lawsuit press conference:

    Professor Fukushima: We have already started to study vaccine harms, basically in cooperation with various experts. This is the first topic. So, we will find out later on what happens after vaccination as a mechanism, i.e., as a pathological and cytological process. Around April last year, the pathology and forensic societies have already issued statements that, in the future, autopsies should be done on people who have died after vaccination. In the future, we need to urgently establish guidelines on what kind of medical treatment should be provided for victims injured by vaccines, and we need to develop diagnostic techniques. Given the situation, we will carry out these tasks.

    One more thing. Pathological autopsies have already been conducted on people who died after receiving the vaccine. However, the Health Ministry is still unwilling to acknowledge the causal link between the vaccine and the deaths. If the Health Ministry maintains this unjustified position, we intend to file additional lawsuits in consultation with our lawyers. We demand that the Health Ministry provides appropriate victim compensation based on the vaccination law. In other words, victim compensation based on the Vaccination Law is properly stipulated by Japanese law. So, it is not necessary to create a new law to compensate for the vaccine harm. Scientists like us are taking responsible actions in every respect to ensure that the vaccine victims are compensated.

    Journalist: Let me ask you a few questions. In your editorial, Professor Fukushima, you wrote two strong statements to all healthcare workers: a warning about the safety of vaccines and a request to stop vaccinations. For example, medical societies are flooded with case reports of various diseases in addition to myocarditis and shingles all over Japan. A huge number of case reports, more than 300 reports by medical experts have been released all over Japan. I consider that this is an extraordinary alarming situation. What is your message to the medical professionals?

    Professor Fukushima: I want to say one thing very clearly to the Health Ministry in addition to the medical professionals. They should distribute a Vaccination Victim’s Handbook to everyone who has been vaccinated. The Vaccination Victim’s Handbook is similar to the Atomic Bomb Victim’s Handbook which is distributed to survivors of the atomic bombs. After distributing the Vaccination Victim’s handbook to vaccinated people, medical institutions should be encouraged to properly follow up with the vaccinated people. It is necessary to examine whether there is a link between the disease and the vaccine. Biopsy tests should be performed on sick people suspected of vaccine induced illness.

    A different clip with English subtitles can be found here:




    References:

    [i] https://twitter.com/ShortShort_News/status/1622224704064098304

    [ii] https://youtube.com/watch?v=GCPaPaAEP4g 【公式】2023.2.2福島雅典教授、厚労省に対する訴訟記者会見ハイライト (English with Japanese subtitles). Full press conference in Japanese available at https://nicovideo.jp/watch/so41730996

    Share







    https://infogame.substack.com/p/japanese-professor-files-lawsuit

    February 2nd 2023: Professor Fukushima held the press conference for his lawsuit at the Tokyo District Court.
    In addition to the lawsuit demands previously mentioned, he also warned that additional lawsuits may be filed if the Japanese MHLW does not acknowledge a causal link between the vaccine and their associated deaths

    https://donshafi911.blogspot.com/2024/02/japanese-professor-files-lawsuit.html
    Japanese professor files lawsuit against Ministry of Health regarding vaccine safety and efficacy! John Smith Masanori Fukushima (福島雅典), professor emeritus at Kyoto University in Japan, has filed a lawsuit against the Japanese Ministry of Health, Labor, and Welfare (MHLW).[i] https://twitter.com/ShortShort_News/status/1622224704064098304 - Click image to watch a clip of the conference The lawsuit seeks the following: The disclosure of all safety and efficacy data of the covid-19 vaccines, submitted by Pfizer and Moderna to the MHLW and the PMDA (Japanese pharmaceutical and medical device regulation agency similar to the FDA) Full disclosure of the contracts between Japan and the pharmaceutical companies (i.e., Pfizer, Moderna, etc.) Compensation for those injured by the covid-19 vaccines Professor Fukushima has over 25 years of experience as an oncologist, and is also the Director and Chairman of the Translational Research Informatics Center in Japan, which is the first academic center in Japan dedicated to transforming basic medical research into clinical practices. He also became involved in pharmacoepidemiology (the study of interactions between drugs and human populations) since 2000. Professor Fukushima in a recent Japanese interview https://www.nicovideo.jp/watch/sm41745638 Professor Fukushima is director of the TRI https://advances.tri-kobe.org/en/feature/11/from-lab-to-clinic.html In November 2022, Professor Fukushima had previously hosted a discussion with other doctors and professors where he condemned the Japanese MHLW for ignoring the dangers of the covid-19 vaccines. Professor Fukushima had demanded investigations into all covid-19 vaccine injuries in a thorough case by case evaluation of medical records. He also warned of the indefinite production of spike proteins via the covid-19 vaccines, as well as the side effects due to lipid nanoparticles. https://rumble.com/v1yofle-japanese-professor-rebukes-ministry-of-health-dissolve-vaccine-committiee-i.html Then in December 2022, Professor Fukushima had stated in an interview his intention to sue the Japanese government because its refusal to disclose vital information regarding the efficacy of the covid-19 vaccines. Which brings us to the current situation where on February 2nd 2023, Professor Fukushima held the press conference for his lawsuit at the Tokyo District Court. In addition to the lawsuit demands previously mentioned, he also warned that additional lawsuits may be filed if the Japanese MHLW does not acknowledge a causal link between the vaccine and their associated deaths. Professor Fukushima skeptically questions the actual result of the 90 trillion yen spent by the government on the covid-19 vaccines. Speaking not only as a doctor and scientist, but also as a citizen and taxpayer, he sees it as part of his duty on behalf of the nation to understand the real effect of the vaccines. He believes surprising information will be revealed from the disclosure of the documents from the pharmaceutical manufacturing companies. He is also studying the pathological mechanisms of the vaccines with other experts as well as medical guidelines for the treatment of vaccine injuries.[ii] Japanese law already stipulates compensation for the vaccine injured, so Professor Fukushima argues that it should be applied now. The Japanese vaccination law outlines the scope of benefits as follows (computer translation from their website): https://elaws.e-gov.go.jp/document?lawid=323AC0000000068 Below is a transcript of a clip of the February 2023 lawsuit press conference: Professor Fukushima: We have already started to study vaccine harms, basically in cooperation with various experts. This is the first topic. So, we will find out later on what happens after vaccination as a mechanism, i.e., as a pathological and cytological process. Around April last year, the pathology and forensic societies have already issued statements that, in the future, autopsies should be done on people who have died after vaccination. In the future, we need to urgently establish guidelines on what kind of medical treatment should be provided for victims injured by vaccines, and we need to develop diagnostic techniques. Given the situation, we will carry out these tasks. One more thing. Pathological autopsies have already been conducted on people who died after receiving the vaccine. However, the Health Ministry is still unwilling to acknowledge the causal link between the vaccine and the deaths. If the Health Ministry maintains this unjustified position, we intend to file additional lawsuits in consultation with our lawyers. We demand that the Health Ministry provides appropriate victim compensation based on the vaccination law. In other words, victim compensation based on the Vaccination Law is properly stipulated by Japanese law. So, it is not necessary to create a new law to compensate for the vaccine harm. Scientists like us are taking responsible actions in every respect to ensure that the vaccine victims are compensated. Journalist: Let me ask you a few questions. In your editorial, Professor Fukushima, you wrote two strong statements to all healthcare workers: a warning about the safety of vaccines and a request to stop vaccinations. For example, medical societies are flooded with case reports of various diseases in addition to myocarditis and shingles all over Japan. A huge number of case reports, more than 300 reports by medical experts have been released all over Japan. I consider that this is an extraordinary alarming situation. What is your message to the medical professionals? Professor Fukushima: I want to say one thing very clearly to the Health Ministry in addition to the medical professionals. They should distribute a Vaccination Victim’s Handbook to everyone who has been vaccinated. The Vaccination Victim’s Handbook is similar to the Atomic Bomb Victim’s Handbook which is distributed to survivors of the atomic bombs. After distributing the Vaccination Victim’s handbook to vaccinated people, medical institutions should be encouraged to properly follow up with the vaccinated people. It is necessary to examine whether there is a link between the disease and the vaccine. Biopsy tests should be performed on sick people suspected of vaccine induced illness. A different clip with English subtitles can be found here: References: [i] https://twitter.com/ShortShort_News/status/1622224704064098304 [ii] https://youtube.com/watch?v=GCPaPaAEP4g 【公式】2023.2.2福島雅典教授、厚労省に対する訴訟記者会見ハイライト (English with Japanese subtitles). Full press conference in Japanese available at https://nicovideo.jp/watch/so41730996 Share https://infogame.substack.com/p/japanese-professor-files-lawsuit February 2nd 2023: Professor Fukushima held the press conference for his lawsuit at the Tokyo District Court. In addition to the lawsuit demands previously mentioned, he also warned that additional lawsuits may be filed if the Japanese MHLW does not acknowledge a causal link between the vaccine and their associated deaths https://donshafi911.blogspot.com/2024/02/japanese-professor-files-lawsuit.html
    INFOGAME.SUBSTACK.COM
    Japanese professor files lawsuit against Ministry of Health regarding vaccine safety and efficacy!
    Masanori Fukushima (福島雅典), professor emeritus at Kyoto University in Japan, has filed a lawsuit against the Japanese Ministry of Health, Labor, and Welfare (MHLW).[i] The lawsuit seeks the following: The disclosure of all safety and efficacy data of the covid-19 vaccines, submitted by Pfizer and Moderna to the MHLW and the PMDA (Japanese pharmaceutical and medical device regulation agency similar to the FDA)
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  • http://www.naturalnews.com/2024-02-01-moderna-online-censorship-agenda-newly-released-documents.html
    http://www.naturalnews.com/2024-02-01-moderna-online-censorship-agenda-newly-released-documents.html
    WWW.NATURALNEWS.COM
    PHARMA OVERLORDS: Moderna’s online censorship agenda detailed in newly released documents – NaturalNews.com
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  • Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule
    A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use.

    Brenda Baletti, Ph.D.
    global moratorium mrna covid vaccine feature
    Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

    Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science.

    Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review.

    The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule.

    After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail.

    Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs).

    Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials.

    They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.”

    They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters.

    “It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote.

    Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies.

    It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender.

    “Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added.

    According to McCollough, “mRNA should never have been authorized for human use.”

    Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.”

    Here are six takeaways from the review:

    1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner

    Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years.

    To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote.

    The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease.

    However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines.

    There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction.

    The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself.

    The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.”

    The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added.

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    2. Steps were taken in trials to overestimate vaccine efficacy

    Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do.

    “No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote.

    Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.”

    Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19.

    There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%.

    The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety.

    Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote.

    Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine.

    The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate.

    One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large.

    According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility.

    While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively.

    “A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote.

    As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death.

    However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote.

    And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.”

    They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19.

    One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19.

    A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues.

    3. The trials underestimated the adverse events, including death, despite evidence in the data.

    Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here.

    First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group.

    “Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked.

    Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population.

    None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote.

    Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended.

    During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data.

    And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports.

    Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.”

    In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.”

    This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.”

    4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary.

    Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population.

    The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants.

    Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.”

    After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke.

    And millions of AEs have been reported to those systems.

    Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system.

    In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervous, immune, reproductive and other systems.

    The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious.

    In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal.

    “The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.”

    5. The failure to appropriately test for safety and toxicity poses serious problems.

    Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs.

    Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues.

    That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids.

    Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown.

    McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns.

    Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time

    This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown.

    6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness.

    The review points readers to a series of papers that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines.

    “The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection.

    They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself.

    They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants.

    https://childrenshealthdefense.org/defender/scientists-global-moratorium-mrna-vaccines-removal-childhood-schedule/


    https://donshafi911.blogspot.com/2024/01/scientists-call-for-global-moratorium.html
    Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use. Brenda Baletti, Ph.D. global moratorium mrna covid vaccine feature Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science. Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review. The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule. After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail. Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs). Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials. They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.” They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters. “It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote. Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies. It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender. “Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added. According to McCollough, “mRNA should never have been authorized for human use.” Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.” Here are six takeaways from the review: 1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years. To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote. The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease. However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines. There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction. The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself. The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.” The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now 2. Steps were taken in trials to overestimate vaccine efficacy Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do. “No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote. Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.” Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19. There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%. The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety. Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote. Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine. The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate. One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large. According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility. While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively. “A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote. As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death. However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote. And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.” They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19. One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19. A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues. 3. The trials underestimated the adverse events, including death, despite evidence in the data. Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here. First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group. “Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked. Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population. None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote. Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended. During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data. And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports. Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.” In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.” This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.” 4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary. Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population. The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants. Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.” After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke. And millions of AEs have been reported to those systems. Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system. In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervous, immune, reproductive and other systems. The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious. In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal. “The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.” 5. The failure to appropriately test for safety and toxicity poses serious problems. Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs. Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues. That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids. Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown. McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns. Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown. 6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness. The review points readers to a series of papers that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines. “The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection. They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself. They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants. https://childrenshealthdefense.org/defender/scientists-global-moratorium-mrna-vaccines-removal-childhood-schedule/ https://donshafi911.blogspot.com/2024/01/scientists-call-for-global-moratorium.html
    CHILDRENSHEALTHDEFENSE.ORG
    Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule
    A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use.
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  • Did COVID-mRNA technology (Malone, Bourla, Bancel, Weissman et al.) vaccine maker MODERNA (Bancel) monitor us? spy on critics of the COVID mRNA vaccine? Yes, it did! should they be shut down? Yes!

    https://palexander.substack.com/p/did-covid-mrna-technology-malone

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    Did COVID-mRNA technology (Malone, Bourla, Bancel, Weissman et al.) vaccine maker MODERNA (Bancel) monitor us? spy on critics of the COVID mRNA vaccine? Yes, it did! should they be shut down? Yes! https://palexander.substack.com/p/did-covid-mrna-technology-malone Join 👇🏻 https://t.me/DrPaulAlexander
    PALEXANDER.SUBSTACK.COM
    Did COVID-mRNA technology (Malone, Bourla, Bancel, Weissman et al.) vaccine maker MODERNA (Bancel) monitor us? spy on critics of the COVID mRNA vaccine? Yes, it did! should they be shut down? Yes!
    Prison? Yes, all of the, Bancel first. He is among the 43 Horsemen of the COVID Apocalypse. We must go after these criminals, investigate them, imprison them if judges say so...
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  • Researchers urge governments to endorse a global moratorium on mRNA injections in a newly released science paper
    Rhoda WilsonJanuary 26, 2024
    In a paper published on Wednesday, researchers re-analysed the Pfizer covid “vaccine” phase 3 trial data and found more serious adverse events among those in the vaccine group.

    This is not what published reports from Pfizer’s phase 3 trials said. “Many key trial findings were either misreported or omitted entirely from published reports,” the researchers said.

    Seven researchers – M. Nathaniel Mead, Stephanie Seneff, Russ Wolfinger, Jessica Rose, Kris Denhaerynck, Steve Kirsch and Peter A. McCullough – set out to re-analyse Pfizer’s trial data because:

    our understanding of covid vaccinations and their impact on health and mortality has evolved substantially since the first vaccine rollouts; and,
    problems with the methods, execution, and reporting of the pivotal phase 3 trials have emerged.
    On Wednesday, they published their findings in a peer-reviewed paper titled ‘Covid-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign’. The paper was published in Cureus, a journal of medical science.

    “Re-analysis of the Pfizer trial data identified statistically significant increases in serious adverse events (SAEs) in the vaccine group,” the researchers wrote.

    Adding, “Numerous SAEs were identified following the Emergency Use Authorisation (EUA), including death, cancer, cardiac events, and various autoimmune, haematological, reproductive, and neurological disorders.”

    The EUA the researchers are referring to is the authorisation granted to Pfizer by the US Food and Drugs Administration (“FDA”).

    As the paper noted, Pfizer’s covid “vaccines” never underwent adequate safety and toxicological testing according to previously established scientific standards. It goes on to detail the absolute risk reduction, the underreporting of harms during trials, the shifting narratives and illusions of protection, quality control and manufacturing process-related impurities, the biological mechanisms underlying adverse events (“AEs”) and why, based on how our immune systems work, the vaccine is ineffective.

    Concluding their comprehensive review, the researchers wrote:

    Given the extensive, well-documented SAEs and unacceptably high harm-to-reward ratio, we urge governments to endorse a global moratorium on the modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered.

    Mead M, Seneff S, Wolfinger R, et al. (January 24, 2024) COVID-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign. Cureus 16(1): e52876. doi:10.7759/cureus.52876none
    Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox…

    The paper noted that the gene therapy products (“GTPs”) vaccine platform has been studied for over 30 years as an experimental cancer treatment, with the terms “gene therapy” and “mRNA vaccination” often used interchangeably.

    “Although we employ the terms ‘vaccine’ and ‘vaccination’ throughout this paper, the covid-19 mRNA products are also accurately termed gene therapy products (GTPs) because, in essence, this was a case of GTP technology being applied to vaccination,” they wrote.

    As such, throughout their analysis, the terms “vaccines” and “vaccinations” are used interchangeably with injections, inoculations, biologicals, or simply, products.

    The following are some excerpts from the paper. You can read the full paper HERE.

    Serious Harms Revealed after EUA was Granted

    In this narrative review, we revisit the registrational trials and review analyses of the AEs from these trials and other relevant studies. Most of the revelations have only recently come to light, due to the past few years of extensive censorship of healthcare professionals and research scientists who challenged the prevailing narrative set forth by the vaccine enterprise.

    Despite the rhetoric, no large randomised double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalisation or death.

    The study designs for the pivotal trials that led to the EUA were never intended to determine whether the mRNA inoculations could help prevent severe disease or premature death.

    It was only after the EUA that the serious biological consequences of rushing the trials became evident, with numerous cardiovascular, neurological, reproductive, haematological, malignant, and autoimmune SAEs identified and published in the peer-reviewed medical literature.

    Moreover, the covid mRNA vaccines produced via Process 1 and evaluated in the trials were not the same products eventually distributed worldwide; all of the covid-19 mRNA products released to the public were produced via Process 2 and have been shown to have varying degrees of DNA contamination.

    The process-related impurities were absent from the covid-19 mRNA products used in the registrational trials. Virtually all doses used in those trials originated from “clinical batches” produced using what is known as Process 1. As a post-authorisation emergency supply measure for global distribution, however, a method much more suitable for mass production known as Process 2 was devised utilising bacterial plasmid DNA.

    The failure of regulatory authorities to heretofore disclose process-related impurities (e.g., SV40) has further increased concerns regarding safety and quality control oversight of mRNA vaccine manufacturing processes.

    Incentives Played a Key Role in Undermining Scientific Evaluation

    Political and financial incentives may have played a key role in undermining the scientific evaluation process leading up to the EUA.

    Before the pandemic, the US National Institutes of Health invested $116 million (35%) in mRNA vaccine technology, the Biomedical Advanced Research and Development Authority (“BARDA”) had invested $148 million (44%), while the Department of Defence (“DOD”) contributed $72 million (21%) to mRNA vaccine development.

    BARDA and the DOD also collaborated closely in the co-development of Moderna’s mRNA vaccine, dedicating over $18 billion, which included guaranteed vaccine purchases. This entailed pre-purchasing hundreds of millions of mRNA vaccine doses, alongside direct financial support for the clinical trials and the expansion of Moderna’s manufacturing capabilities.

    Once the pandemic began, $29.2 billion – 92% of which came from US public funds – was dedicated to the purchase of covid-19 mRNA products; another $2.2 billion (7%) was channelled into supporting clinical trials, and $108 million (less than 1%) was allocated for manufacturing and basic research.

    Using US taxpayer money to purchase so many doses in advance would suggest that, before the EUA process, US federal agencies were strongly biased toward successful outcomes for the registrational trials.

    Established Vaccine Testing Period Abolished

    Before the rapid authorisation process, no vaccine had been permitted for market release without undergoing a testing period of at least four years. Previous timeframes for phase 3 trial testing averaged 10 years. Health departments have stated that 10-15 years is the normal timeframe for evaluating vaccine safety.

    The previously established 10-15-year timeframe for clinical evaluation of vaccines was deemed necessary to ensure adequate time for monitoring the development of AEs such as cancers and autoimmune disorders.

    Pfizer’s covid vaccine completed the process in seven months.

    Established Safety Standards Abolished

    With the covid vaccines, safety was never assessed in a manner commensurate with previously established scientific standards, as numerous safety testing and toxicology protocols typically followed by the FDA were sidestepped.

    Historical accounts bear witness to instances where vaccines were prematurely introduced to the market under immense pressure, only to reveal disabling or even fatal AEs later on. Examples include the 1955 contamination of polio vaccines, instances of Guillain-Barré syndrome observed in flu vaccine recipients in 1976, and the connection between narcolepsy and a specific flu vaccine in 2009.

    Against this backdrop, it is not surprising that so many medical and public health experts voiced concerns about covid mRNA vaccines bypassing the normal safety testing process.

    Concerns about inadequate safety testing extend beyond the usual regulatory approval standards and practices.

    As there were no specific regulations at the time of the rapid approval process, regulatory agencies quickly “adapted” the products, generalised the definition of “vaccine” to accommodate them, and then authorised them for EUA for the first time ever against a viral disease.

    Due to the GTPs’ reclassification as vaccines, none of their components have been thoroughly evaluated for safety. The main concern, in a nutshell, is that the covid mRNA products may transform body cells into viral protein factories that have no off-switch – i.e., no built-in mechanism to stop or regulate such proliferation – with the spike protein (“S-protein”) being generated for prolonged periods, causing chronic, systemic inflammation and immune dysfunction.

    When the S-protein enters the bloodstream and disseminates systemically, it may become a contributing factor to diverse AEs in susceptible people.

    Enforce a Global Moratorium

    Given the well-documented SAEs and unacceptable harm-to-reward ratio, we urge governments to endorse and enforce a global moratorium on these modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered.



    https://expose-news.com/2024/01/26/researchers-urge-a-global-moratorium-on-mrna/
    Researchers urge governments to endorse a global moratorium on mRNA injections in a newly released science paper Rhoda WilsonJanuary 26, 2024 In a paper published on Wednesday, researchers re-analysed the Pfizer covid “vaccine” phase 3 trial data and found more serious adverse events among those in the vaccine group. This is not what published reports from Pfizer’s phase 3 trials said. “Many key trial findings were either misreported or omitted entirely from published reports,” the researchers said. Seven researchers – M. Nathaniel Mead, Stephanie Seneff, Russ Wolfinger, Jessica Rose, Kris Denhaerynck, Steve Kirsch and Peter A. McCullough – set out to re-analyse Pfizer’s trial data because: our understanding of covid vaccinations and their impact on health and mortality has evolved substantially since the first vaccine rollouts; and, problems with the methods, execution, and reporting of the pivotal phase 3 trials have emerged. On Wednesday, they published their findings in a peer-reviewed paper titled ‘Covid-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign’. The paper was published in Cureus, a journal of medical science. “Re-analysis of the Pfizer trial data identified statistically significant increases in serious adverse events (SAEs) in the vaccine group,” the researchers wrote. Adding, “Numerous SAEs were identified following the Emergency Use Authorisation (EUA), including death, cancer, cardiac events, and various autoimmune, haematological, reproductive, and neurological disorders.” The EUA the researchers are referring to is the authorisation granted to Pfizer by the US Food and Drugs Administration (“FDA”). As the paper noted, Pfizer’s covid “vaccines” never underwent adequate safety and toxicological testing according to previously established scientific standards. It goes on to detail the absolute risk reduction, the underreporting of harms during trials, the shifting narratives and illusions of protection, quality control and manufacturing process-related impurities, the biological mechanisms underlying adverse events (“AEs”) and why, based on how our immune systems work, the vaccine is ineffective. Concluding their comprehensive review, the researchers wrote: Given the extensive, well-documented SAEs and unacceptably high harm-to-reward ratio, we urge governments to endorse a global moratorium on the modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered. Mead M, Seneff S, Wolfinger R, et al. (January 24, 2024) COVID-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign. Cureus 16(1): e52876. doi:10.7759/cureus.52876none Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… The paper noted that the gene therapy products (“GTPs”) vaccine platform has been studied for over 30 years as an experimental cancer treatment, with the terms “gene therapy” and “mRNA vaccination” often used interchangeably. “Although we employ the terms ‘vaccine’ and ‘vaccination’ throughout this paper, the covid-19 mRNA products are also accurately termed gene therapy products (GTPs) because, in essence, this was a case of GTP technology being applied to vaccination,” they wrote. As such, throughout their analysis, the terms “vaccines” and “vaccinations” are used interchangeably with injections, inoculations, biologicals, or simply, products. The following are some excerpts from the paper. You can read the full paper HERE. Serious Harms Revealed after EUA was Granted In this narrative review, we revisit the registrational trials and review analyses of the AEs from these trials and other relevant studies. Most of the revelations have only recently come to light, due to the past few years of extensive censorship of healthcare professionals and research scientists who challenged the prevailing narrative set forth by the vaccine enterprise. Despite the rhetoric, no large randomised double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalisation or death. The study designs for the pivotal trials that led to the EUA were never intended to determine whether the mRNA inoculations could help prevent severe disease or premature death. It was only after the EUA that the serious biological consequences of rushing the trials became evident, with numerous cardiovascular, neurological, reproductive, haematological, malignant, and autoimmune SAEs identified and published in the peer-reviewed medical literature. Moreover, the covid mRNA vaccines produced via Process 1 and evaluated in the trials were not the same products eventually distributed worldwide; all of the covid-19 mRNA products released to the public were produced via Process 2 and have been shown to have varying degrees of DNA contamination. The process-related impurities were absent from the covid-19 mRNA products used in the registrational trials. Virtually all doses used in those trials originated from “clinical batches” produced using what is known as Process 1. As a post-authorisation emergency supply measure for global distribution, however, a method much more suitable for mass production known as Process 2 was devised utilising bacterial plasmid DNA. The failure of regulatory authorities to heretofore disclose process-related impurities (e.g., SV40) has further increased concerns regarding safety and quality control oversight of mRNA vaccine manufacturing processes. Incentives Played a Key Role in Undermining Scientific Evaluation Political and financial incentives may have played a key role in undermining the scientific evaluation process leading up to the EUA. Before the pandemic, the US National Institutes of Health invested $116 million (35%) in mRNA vaccine technology, the Biomedical Advanced Research and Development Authority (“BARDA”) had invested $148 million (44%), while the Department of Defence (“DOD”) contributed $72 million (21%) to mRNA vaccine development. BARDA and the DOD also collaborated closely in the co-development of Moderna’s mRNA vaccine, dedicating over $18 billion, which included guaranteed vaccine purchases. This entailed pre-purchasing hundreds of millions of mRNA vaccine doses, alongside direct financial support for the clinical trials and the expansion of Moderna’s manufacturing capabilities. Once the pandemic began, $29.2 billion – 92% of which came from US public funds – was dedicated to the purchase of covid-19 mRNA products; another $2.2 billion (7%) was channelled into supporting clinical trials, and $108 million (less than 1%) was allocated for manufacturing and basic research. Using US taxpayer money to purchase so many doses in advance would suggest that, before the EUA process, US federal agencies were strongly biased toward successful outcomes for the registrational trials. Established Vaccine Testing Period Abolished Before the rapid authorisation process, no vaccine had been permitted for market release without undergoing a testing period of at least four years. Previous timeframes for phase 3 trial testing averaged 10 years. Health departments have stated that 10-15 years is the normal timeframe for evaluating vaccine safety. The previously established 10-15-year timeframe for clinical evaluation of vaccines was deemed necessary to ensure adequate time for monitoring the development of AEs such as cancers and autoimmune disorders. Pfizer’s covid vaccine completed the process in seven months. Established Safety Standards Abolished With the covid vaccines, safety was never assessed in a manner commensurate with previously established scientific standards, as numerous safety testing and toxicology protocols typically followed by the FDA were sidestepped. Historical accounts bear witness to instances where vaccines were prematurely introduced to the market under immense pressure, only to reveal disabling or even fatal AEs later on. Examples include the 1955 contamination of polio vaccines, instances of Guillain-Barré syndrome observed in flu vaccine recipients in 1976, and the connection between narcolepsy and a specific flu vaccine in 2009. Against this backdrop, it is not surprising that so many medical and public health experts voiced concerns about covid mRNA vaccines bypassing the normal safety testing process. Concerns about inadequate safety testing extend beyond the usual regulatory approval standards and practices. As there were no specific regulations at the time of the rapid approval process, regulatory agencies quickly “adapted” the products, generalised the definition of “vaccine” to accommodate them, and then authorised them for EUA for the first time ever against a viral disease. Due to the GTPs’ reclassification as vaccines, none of their components have been thoroughly evaluated for safety. The main concern, in a nutshell, is that the covid mRNA products may transform body cells into viral protein factories that have no off-switch – i.e., no built-in mechanism to stop or regulate such proliferation – with the spike protein (“S-protein”) being generated for prolonged periods, causing chronic, systemic inflammation and immune dysfunction. When the S-protein enters the bloodstream and disseminates systemically, it may become a contributing factor to diverse AEs in susceptible people. Enforce a Global Moratorium Given the well-documented SAEs and unacceptable harm-to-reward ratio, we urge governments to endorse and enforce a global moratorium on these modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered. https://expose-news.com/2024/01/26/researchers-urge-a-global-moratorium-on-mrna/
    EXPOSE-NEWS.COM
    Researchers urge governments to endorse a global moratorium on mRNA injections in a newly released science paper
    In a paper published on Wednesday, researchers re-analysed the Pfizer covid “vaccine” phase 3 trial data and found more serious adverse events among those in the vaccine group. This is not what pub…
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  • Terrifying! New LETHAL BIO-WEAPON SARS-COV-3 Built and Hid by CHINA’s ARMY | VT Foreign Policy
    January 24, 2024
    VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel

    $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts
    Source: Embassy of Israel, Washington, D.C. and US Department of State.

    by Fabio Giuseppe Carlo Carisio

    VERSIONE IN ITALIANO

    The news is much more alarming than the mysterious and lethal Virus with which Bill Gates and his accomplices at the World Economic Forum have continued to threaten humanity for almost a year to push all governments to accept the Pandemic Treaty of the World Health Organization (financed by Bill & Melinda Gates Foundation), the international Vaccine Passport following the example of the European Union’s Green Pass and, consequently, a new wave of mandatory vaccinations to implement the global immunization plan launched by the Microsoft’s tycoon in 1999 in the Congress Center of Rockefeller in the Villa Serbelloni in Bellagio (Como).

    Perhaps it could be this new version of SARS-Cov-2, engineered in a laboratory at Being University and so powerful that it can be defined as SARS-Cov-3 due to its multiple mutations, the mysterious Disease X!

    Indeed after the investigation by Gospa News (published in Italian only), the study was modified, making the most alarming parts disappear…

    The suspicion comes from 4 disturbing circumstances that make the new, very dangerous Chinese research a real BIO-WEAPON capable of threatening all of humanity.

    It was developed with the help of military doctors of PLA: People’s Liberation Army of China.
    The laboratory experiments showed a lethality of 100% on humanized mice
    The research was carried out based on previous virological tests conducted by zoologist Shi Zhengli of the Wuhan Institute of Virology
    On January 21, 2024, the authors have modified the study by eliminating any terrifying reference to the 100% mortality on humanized mice, two days after the publication of the Gospa News investigation! Fortunately we have preserved both the screenshots and the original PDF study…
    A first study was published on December 18, 2022 in the specialized journal Emerging Microbes & Infections and on the same date also on PubMed, the library of the National Institute for Health (NIH) of the US Department of Health, but only in the update of a few days ago the lethality of the laboratory genotype of SARS-Cov-2 called GX_P2V was made known when the new research was relaunched the first time on January 4th in pre-print by BioRxivwhere it has yet to be subjected to peer review.

    The Abstract of the research up to January 21st was as brief as it was chilling:

    «SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) can cause 100% mortality in human ACE2-transgenic mice, potentially attributable to late-stage brain infection. This underscores a spillover risk of GX_P2V into humans and provides a unique model for understanding the pathogenic mechanisms of SARS-CoV-2-related viruses».


    The study published on January 4th from which the role of a military doctor from the Beijing General Hospital of the PLA army can be deduced and, alongside, the study modified on January 21st with a new title and a new Abstract from which the alarm about 100% lethality in humanized mice disappeared
    The updated study instead appears with a new, less alarming title “An infection and pathogenesis mouse model of SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR)” has also been sweetened in the ABSTRACT from which any reference to the VERY HIGH LETHALITY of the virus created in the laboratory DISAPPEARS:

    «SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) is highly attenuated, but can cause mortality in a specifically designed human ACE2-transgenic mouse model, making it an invaluable surrogate model for evaluating the efficacy of drugs and vaccines against SARS-CoV-2».

    Even more so after this SELF-CENSORSHIP, the previous original document that we wrote about takes on importance and on which we believe it is our duty to focus even if the researchers will obviously be able to claim that they are wrong…

    The study by Lai Wei et al. was conducted by Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Life Science and Technology, Beijing University of Chemical Technology (China), with the collaboration of State Key Laboratory of Pharmaceutical Biotechnology, Medical School, Nanjing University, but also with Research Center for Clinical Medicine, The Fifth Medical Center of PLA General Hospital, Beijing, where the military doctor Shengdong Luo, present in both studies, and his colleague Weiwei Chen work.

    The latter is one of the various military hospitals that have taken the place of civilian facilities since 2016 as confirmed by a photo of the inauguration found on the internet.


    One of Beijing’s civilian hospitals converted into a military facility in 2016
    One of the most disturbing aspects of this research is the fact that it derives from the previous study published in 2022 which highlighted only research aimed at producing a vaccine. While this new in-depth study has in fact transformed the study into the typology products defined in the US as “Dual Use Research of Concern (DURC)”where the dual utility consists precisely in the use as a vaccine or as a bio-weapon.

    From the “Smoking Gun” of Artificial SARS-Cov-2 to Beijing’s New Bio-Weapon

    This new and very dangerous experiment brings us back to the studies on chimeric coronaviruses at the Wuhan Institute of Virology where the scientist Shi Zhengli infected SARS strains with HIV plasmids since 2004 thanks to the funding of the Episars project of the European Commission chaired by Romano Prodi to experiment with an artificial enhancement of the wild virus which culminated in the so-called “smoking gun” on the origin of SARS-Cov-2 of Covid 19.

    «When I first saw the furin cleavage site in the viral sequence (of SARS-Cov-2 – ed.), with its arginine codons, I told my wife that it was the smoking gun for the origin of the virus”.

    This is what Dr. David Baltimore, a renowned American virologist and co-discoverer of reverse transcriptase, stated in support of the thesis (now much more than a theory) of the artificial origin of the pandemic pathogen which, to summarize it in a simple way , attaches itself to human cells and becomes lethal precisely thanks to that criticality in furin.

    Proof of this laboratory alteration emerged from a 2016 study, which remained almost unknown until recently, which was financed by the virologist Antony Fauci (former director of the American National Institute of Allergy and Infectious Diseases – NIAID) and conducted by US scientists, Wuhan researchers and Chinese medical doctors as revealed by the dossier of the US Senate Health Committee which not only ascertained the high probability of the artificial origin of SARS-Cov-2 but highlighted the role of American researchers…

    It is now known that Fauci himself admitted before the American Congress that the theory of the virus built in the laboratory is not a conspiracy as he instead claimed in a study on natural origins published shortly after some Indian scientists from the Kusuma School of Biology in New Delhi discovered the anomalous HIV sequences and reported them in a paper published in ResearchGate.

    But “they were then forced to withdraw” according to the late biologist Luc Montagnier, who was the first to publish research on artificial origin together with his biomathematician friend Jean-Claude Perez whom Gospa News interviewed exclusively a few months ago.

    In our investigations of the Wuhan-Gates cycle (in homage to Bill Gates who financed the Wuhan projects through EcoHealthAliance) we highlighted how the collaboration between the US and China started on biological weapons by former presidents Bill Clinton and Jiang Zemin was fundamental to the Predict-2 project on chimeric coronavirus researches funded by the Obama-Biden administration.

    This is why we have embraced the thesis of the patent expert David E. Martin who supported something very serious: according to him, in fact, the SARS-Cov-2 built between China and the US (but probably with contributions also in Canada, the United Kingdom and Ukraine) was allegedly intentionally released by the United States of America. In fact, it has brought to light too many intrigues between the research of Moderna Big Pharma (also financed by Gates and Fauci) and the Pentagon’s military agency DARPA.

    So China (led by Xi Jinping disliked by the Shanghai Clan of Jiang Zemin’s political heirs and his son who strengthened the Wuhan Institute of Virology) would have suffered, for the second time after the SARS of 2003 also built in a laboratory according to Martin and Russian genomics experts, the dispersal of the virus likely occurred during the World Military Games in Wuhan in October 2019.

    This is why, as reported recently by the Wall Street Journal, on the basis of documents obtained from the United States Department of Health, Chinese researchers isolated and mapped the Covid-19 virus at the end of December 2019, at least two weeks before Beijing revealed the details of the deadly virus to the world. According to the US newspaper, a Chinese researcher in Beijing uploaded an almost complete sequence of the structure of Covid into a database managed by the American government on December 28, 2019, while China shared the sequence of the virus with the World Health Organization (WHO) only 11 January 2020.

    In light of these considerations, the new experimentation also conducted by Chinese military doctors takes on an even more disturbing plot. So much so as to fuel the suspicion that Beijing has built a deadly bio-weapon ready to be spread in a global bacteriological war should new Western-inspired pandemics appear.

    Chinese research for a new attenuated vaccine against Covid-19

    Now that we have analyzed the historical and geopolitical context, let’s briefly summarize the peculiarities of the two different studies on SARS-CoV-2 GX_P2V, the one for the 2022 vaccine and the one for the 2023 bioweapon.


    The first research by Beijing University for a new anti-Covid vaccine – link at the bottom of the page
    «SARS-CoV-2 related coronaviruses (SARS-CoV-2r) from Guangdong and Guangxi pangolins have been implicated in the emergence of SARS-CoV-2 and future pandemics. We previously reported the culture of a SARS-CoV-2r GX_P2V from Guangxi pangolins. Here we report the GX_P2V isolate rapidly adapted to Vero cells by acquiring two genomic mutations: an alanine to valine substitution in the nucleoprotein and a 104-nucleotide deletion in the hypervariable region (HVR) of the 3′-terminus untranslated region (3′-UTR)».

    This is what we read in the Abstract on PubMed of December 2022 regarding the research by Shanshan Lu et al. entitled “Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR”.

    «We further report the characterization of the GX_P2V variant (renamed GX_P2V(short_3UTR)) in in vitro and in vivo infection models. In cultured Vero, BGM and Calu-3 cells, GX_P2V(short_3UTR) had similar robust replication kinetics, and consistently produced minimum cell damage. GX_P2V(short_3UTR) infected golden hamsters and BALB/c mice but was highly attenuated. Golden hamsters infected intranasally had a short duration of productive infection in pulmonary, not extrapulmonary, tissues».

    The Abstract then goes into the specifics of the development of an antidote against Covid based not on the new and controversial biotechnology of mRNA gene sera but on that of traditional vaccines:

    «These productive infections induced neutralizing antibodies against pseudoviruses of GX_P2V and SARS-CoV-2. Collectively, our data show that the GX_P2V(short_3UTR) is highly attenuated in in vitro and in vivo infection models. Attenuation of the variant is likely partially due to the 104-nt deletion in the HVR in the 3′-UTR. This study furthers our understanding of pangolin coronaviruses pathogenesis and provides novel insights for the design of live attenuated vaccines against SARS-CoV-2».

    The Army Laboratory Experiment for a Bacteriological Weapon

    The recently published study with the already extremely alarming title “Lethal Infection of Human ACE2- Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR)” had a different impact, before it was altered on January 21 to mitigate its hazard…

    This work was supported by NSFC-MFST project (China–Mongolia) (grant number 32161143027), National Key R&D Program of China (2021YFC2301804) and Biosafety Special Program (No. 19SWAQ 13).

    «Two SARS-CoV-2-related pangolin coronaviruses, GD/2019 and GX/2017, were identified prior to the COVID-19 outbreak (1,2). The respective isolates, termed pCoV-GD01 and GX_P2V, were cultured in 2020 and 2017, respectively (2,3). The infectivity and pathogenicity of these isolates have been studied (4–6). The pCoV-GD01 isolate, which has higher homology with SARS-CoV-2, can infect and cause disease in both golden hamsters and hACE2 mice (4)».

    We read in the pre-print research by Lai Wei et al.:

    «In contrast, while GX_P2V can also infect both species, it does not appear to cause obvious disease in these animals (5,6). We previously reported that the early passaged GX_P2V isolate was actually a cell culture-adapted mutant, named GX_P2V(short_3UTR), which possesses a 104-nucleotide deletion at the 3’-UTR (6). In this study, we cloned this mutant, considering the propensity of coronaviruses to undergo rapid adaptive mutation in cell culture, and assessed its pathogenicity in hACE2 mice. We found that the GX_P2V(short_3UTR) clone can infect hACE2 mice, with high viral loads detected in both lung and brain tissues. This infection resulted in 100% mortality in the hACE2 mice. We surmise that the cause of death may be linked to the occurrence of late brain infection».


    The cover of the study published on January 4 on BiorXiv before the modification on January 21, 2024 – link at the bottom of the page
    Then they also recall that these SARS-CoV-2, GD/2019 and GX/2017 studies were initially carried out by the well-known scientist from the Wuhan Institute of Virology:

    «To the best of our knowledge, this is the first report showing that a SARS-CoV-2-related pangolin coronavirus can cause 100% mortality in hACE2 mice, suggesting a risk for GX_P2V to spill over into humans. Our findings are evidently inconsistent with those of Zhengli Shiet al. (5), who tested the virulence of GX_P2V in two different hACE2 mouse models».

    The discussion then becomes very technical and evidence of expert biochemists or virologists:

    «It is important to note that we did not isolate the wild-type GX_P2V strain. The study by Zhengli Shi et al tested the GX_P2V(short_3UTR) variant that we reported. However, the adaptative evolutionary changes of this variant during their laboratory culture remain understudied. In fact, according to additional infection experiments, the uncloned GX_P2V(short_3UTR) also resulted in 100% mortality in hACE2 mice. Due to the propensity of coronaviruses to undergo adaptive mutation during passage culture, we cloned and analyzed mutations in GX_P2V(short_3UTR), focusing specifically on the pathogenicity of the cloned strains. The high pathogenicity mechanism of GX_P2V C7 in hACE2 mice, in the absence of the wild-type GX_P2V control, requires further investigation».

    And the conclusion doesn’t suggest anything good…

    «Compared to the original sequence of GX_P2V(short_3UTR), GX_P2V C7 has two amino acid mutations in the spike protein. Given the close relationship between coronavirus virulence and spike protein mutations (7), it is possible that GX_P2V C7 has undergone a virulence-enhancing mutation. However, it is important to note that our hACE2 mouse model may be relatively unique. The company has not yet published a paper on this hACE2 mouse model, but our results suggest that hACE2 may be highly expressed in the mouse brain. Additionally, according to the data provided by the company, these hACE2 mice have abnormal physiology, as indicated by relatively reduced serum triglyceride, cholesterol, and lipase levels, compared to those of wild-type C57BL/6J mice. In summary, our study provides a unique perspective on the pathogenicity of GX_P2V and offers a distinct alternative model for understanding the pathogenic mechanisms of SARS-CoV-2-related coronaviruses».

    The scientific explanation is cloaked by a strong emphasis on virulence which may also appear as a “threat” on the possibility of transforming these GX_P2V genotypes into a real bacteriological weapon.

    Fabio Giuseppe Carlo Carisio
    © COPYRIGHT GOSPA NEWS
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    MAIN SOURCES

    PUBMED – Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR’

    BIORXIV – Lethal Infection of Human ACE2-Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR)

    To receive the COMPLETE PDF OF THE ORIGINAL DISTURBING RESEARCH, subscribe to the Gospa News Newsletter and write to redazione@gospanews.net

    GOSPA NEWS – WUHAN-GATES DOSSIER

    GOSPA NEWS – COVID-19 DOSSIER

    Fabio G. C. Carisio
    Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal.

    His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more…

    Most popolar investigation on VT is:

    Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon

    Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting.

    For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime.

    With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians.

    In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence.

    In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates

    His investigations was quoted also by The Gateway Pundit, Tasnim and others

    He worked for many years for the magazine Art & Wine as an art critic and curator.

    VETERANS TODAY OLD POSTS

    www.gospanews.net/


    ATTENTION READERS

    We See The World From All Sides and Want YOU To Be Fully Informed
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    About VT - Policies & Disclosures - Comment Policy
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    https://www.vtforeignpolicy.com/2024/01/terrifying-new-lethal-bio-weapon-sars-cov-3-built-and-hid-by-chinas-army/
    Terrifying! New LETHAL BIO-WEAPON SARS-COV-3 Built and Hid by CHINA’s ARMY | VT Foreign Policy January 24, 2024 VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO The news is much more alarming than the mysterious and lethal Virus with which Bill Gates and his accomplices at the World Economic Forum have continued to threaten humanity for almost a year to push all governments to accept the Pandemic Treaty of the World Health Organization (financed by Bill & Melinda Gates Foundation), the international Vaccine Passport following the example of the European Union’s Green Pass and, consequently, a new wave of mandatory vaccinations to implement the global immunization plan launched by the Microsoft’s tycoon in 1999 in the Congress Center of Rockefeller in the Villa Serbelloni in Bellagio (Como). Perhaps it could be this new version of SARS-Cov-2, engineered in a laboratory at Being University and so powerful that it can be defined as SARS-Cov-3 due to its multiple mutations, the mysterious Disease X! Indeed after the investigation by Gospa News (published in Italian only), the study was modified, making the most alarming parts disappear… The suspicion comes from 4 disturbing circumstances that make the new, very dangerous Chinese research a real BIO-WEAPON capable of threatening all of humanity. It was developed with the help of military doctors of PLA: People’s Liberation Army of China. The laboratory experiments showed a lethality of 100% on humanized mice The research was carried out based on previous virological tests conducted by zoologist Shi Zhengli of the Wuhan Institute of Virology On January 21, 2024, the authors have modified the study by eliminating any terrifying reference to the 100% mortality on humanized mice, two days after the publication of the Gospa News investigation! Fortunately we have preserved both the screenshots and the original PDF study… A first study was published on December 18, 2022 in the specialized journal Emerging Microbes & Infections and on the same date also on PubMed, the library of the National Institute for Health (NIH) of the US Department of Health, but only in the update of a few days ago the lethality of the laboratory genotype of SARS-Cov-2 called GX_P2V was made known when the new research was relaunched the first time on January 4th in pre-print by BioRxivwhere it has yet to be subjected to peer review. The Abstract of the research up to January 21st was as brief as it was chilling: «SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) can cause 100% mortality in human ACE2-transgenic mice, potentially attributable to late-stage brain infection. This underscores a spillover risk of GX_P2V into humans and provides a unique model for understanding the pathogenic mechanisms of SARS-CoV-2-related viruses». The study published on January 4th from which the role of a military doctor from the Beijing General Hospital of the PLA army can be deduced and, alongside, the study modified on January 21st with a new title and a new Abstract from which the alarm about 100% lethality in humanized mice disappeared The updated study instead appears with a new, less alarming title “An infection and pathogenesis mouse model of SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR)” has also been sweetened in the ABSTRACT from which any reference to the VERY HIGH LETHALITY of the virus created in the laboratory DISAPPEARS: «SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) is highly attenuated, but can cause mortality in a specifically designed human ACE2-transgenic mouse model, making it an invaluable surrogate model for evaluating the efficacy of drugs and vaccines against SARS-CoV-2». Even more so after this SELF-CENSORSHIP, the previous original document that we wrote about takes on importance and on which we believe it is our duty to focus even if the researchers will obviously be able to claim that they are wrong… The study by Lai Wei et al. was conducted by Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Life Science and Technology, Beijing University of Chemical Technology (China), with the collaboration of State Key Laboratory of Pharmaceutical Biotechnology, Medical School, Nanjing University, but also with Research Center for Clinical Medicine, The Fifth Medical Center of PLA General Hospital, Beijing, where the military doctor Shengdong Luo, present in both studies, and his colleague Weiwei Chen work. The latter is one of the various military hospitals that have taken the place of civilian facilities since 2016 as confirmed by a photo of the inauguration found on the internet. One of Beijing’s civilian hospitals converted into a military facility in 2016 One of the most disturbing aspects of this research is the fact that it derives from the previous study published in 2022 which highlighted only research aimed at producing a vaccine. While this new in-depth study has in fact transformed the study into the typology products defined in the US as “Dual Use Research of Concern (DURC)”where the dual utility consists precisely in the use as a vaccine or as a bio-weapon. From the “Smoking Gun” of Artificial SARS-Cov-2 to Beijing’s New Bio-Weapon This new and very dangerous experiment brings us back to the studies on chimeric coronaviruses at the Wuhan Institute of Virology where the scientist Shi Zhengli infected SARS strains with HIV plasmids since 2004 thanks to the funding of the Episars project of the European Commission chaired by Romano Prodi to experiment with an artificial enhancement of the wild virus which culminated in the so-called “smoking gun” on the origin of SARS-Cov-2 of Covid 19. «When I first saw the furin cleavage site in the viral sequence (of SARS-Cov-2 – ed.), with its arginine codons, I told my wife that it was the smoking gun for the origin of the virus”. This is what Dr. David Baltimore, a renowned American virologist and co-discoverer of reverse transcriptase, stated in support of the thesis (now much more than a theory) of the artificial origin of the pandemic pathogen which, to summarize it in a simple way , attaches itself to human cells and becomes lethal precisely thanks to that criticality in furin. Proof of this laboratory alteration emerged from a 2016 study, which remained almost unknown until recently, which was financed by the virologist Antony Fauci (former director of the American National Institute of Allergy and Infectious Diseases – NIAID) and conducted by US scientists, Wuhan researchers and Chinese medical doctors as revealed by the dossier of the US Senate Health Committee which not only ascertained the high probability of the artificial origin of SARS-Cov-2 but highlighted the role of American researchers… It is now known that Fauci himself admitted before the American Congress that the theory of the virus built in the laboratory is not a conspiracy as he instead claimed in a study on natural origins published shortly after some Indian scientists from the Kusuma School of Biology in New Delhi discovered the anomalous HIV sequences and reported them in a paper published in ResearchGate. But “they were then forced to withdraw” according to the late biologist Luc Montagnier, who was the first to publish research on artificial origin together with his biomathematician friend Jean-Claude Perez whom Gospa News interviewed exclusively a few months ago. In our investigations of the Wuhan-Gates cycle (in homage to Bill Gates who financed the Wuhan projects through EcoHealthAliance) we highlighted how the collaboration between the US and China started on biological weapons by former presidents Bill Clinton and Jiang Zemin was fundamental to the Predict-2 project on chimeric coronavirus researches funded by the Obama-Biden administration. This is why we have embraced the thesis of the patent expert David E. Martin who supported something very serious: according to him, in fact, the SARS-Cov-2 built between China and the US (but probably with contributions also in Canada, the United Kingdom and Ukraine) was allegedly intentionally released by the United States of America. In fact, it has brought to light too many intrigues between the research of Moderna Big Pharma (also financed by Gates and Fauci) and the Pentagon’s military agency DARPA. So China (led by Xi Jinping disliked by the Shanghai Clan of Jiang Zemin’s political heirs and his son who strengthened the Wuhan Institute of Virology) would have suffered, for the second time after the SARS of 2003 also built in a laboratory according to Martin and Russian genomics experts, the dispersal of the virus likely occurred during the World Military Games in Wuhan in October 2019. This is why, as reported recently by the Wall Street Journal, on the basis of documents obtained from the United States Department of Health, Chinese researchers isolated and mapped the Covid-19 virus at the end of December 2019, at least two weeks before Beijing revealed the details of the deadly virus to the world. According to the US newspaper, a Chinese researcher in Beijing uploaded an almost complete sequence of the structure of Covid into a database managed by the American government on December 28, 2019, while China shared the sequence of the virus with the World Health Organization (WHO) only 11 January 2020. In light of these considerations, the new experimentation also conducted by Chinese military doctors takes on an even more disturbing plot. So much so as to fuel the suspicion that Beijing has built a deadly bio-weapon ready to be spread in a global bacteriological war should new Western-inspired pandemics appear. Chinese research for a new attenuated vaccine against Covid-19 Now that we have analyzed the historical and geopolitical context, let’s briefly summarize the peculiarities of the two different studies on SARS-CoV-2 GX_P2V, the one for the 2022 vaccine and the one for the 2023 bioweapon. The first research by Beijing University for a new anti-Covid vaccine – link at the bottom of the page «SARS-CoV-2 related coronaviruses (SARS-CoV-2r) from Guangdong and Guangxi pangolins have been implicated in the emergence of SARS-CoV-2 and future pandemics. We previously reported the culture of a SARS-CoV-2r GX_P2V from Guangxi pangolins. Here we report the GX_P2V isolate rapidly adapted to Vero cells by acquiring two genomic mutations: an alanine to valine substitution in the nucleoprotein and a 104-nucleotide deletion in the hypervariable region (HVR) of the 3′-terminus untranslated region (3′-UTR)». This is what we read in the Abstract on PubMed of December 2022 regarding the research by Shanshan Lu et al. entitled “Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR”. «We further report the characterization of the GX_P2V variant (renamed GX_P2V(short_3UTR)) in in vitro and in vivo infection models. In cultured Vero, BGM and Calu-3 cells, GX_P2V(short_3UTR) had similar robust replication kinetics, and consistently produced minimum cell damage. GX_P2V(short_3UTR) infected golden hamsters and BALB/c mice but was highly attenuated. Golden hamsters infected intranasally had a short duration of productive infection in pulmonary, not extrapulmonary, tissues». The Abstract then goes into the specifics of the development of an antidote against Covid based not on the new and controversial biotechnology of mRNA gene sera but on that of traditional vaccines: «These productive infections induced neutralizing antibodies against pseudoviruses of GX_P2V and SARS-CoV-2. Collectively, our data show that the GX_P2V(short_3UTR) is highly attenuated in in vitro and in vivo infection models. Attenuation of the variant is likely partially due to the 104-nt deletion in the HVR in the 3′-UTR. This study furthers our understanding of pangolin coronaviruses pathogenesis and provides novel insights for the design of live attenuated vaccines against SARS-CoV-2». The Army Laboratory Experiment for a Bacteriological Weapon The recently published study with the already extremely alarming title “Lethal Infection of Human ACE2- Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR)” had a different impact, before it was altered on January 21 to mitigate its hazard… This work was supported by NSFC-MFST project (China–Mongolia) (grant number 32161143027), National Key R&D Program of China (2021YFC2301804) and Biosafety Special Program (No. 19SWAQ 13). «Two SARS-CoV-2-related pangolin coronaviruses, GD/2019 and GX/2017, were identified prior to the COVID-19 outbreak (1,2). The respective isolates, termed pCoV-GD01 and GX_P2V, were cultured in 2020 and 2017, respectively (2,3). The infectivity and pathogenicity of these isolates have been studied (4–6). The pCoV-GD01 isolate, which has higher homology with SARS-CoV-2, can infect and cause disease in both golden hamsters and hACE2 mice (4)». We read in the pre-print research by Lai Wei et al.: «In contrast, while GX_P2V can also infect both species, it does not appear to cause obvious disease in these animals (5,6). We previously reported that the early passaged GX_P2V isolate was actually a cell culture-adapted mutant, named GX_P2V(short_3UTR), which possesses a 104-nucleotide deletion at the 3’-UTR (6). In this study, we cloned this mutant, considering the propensity of coronaviruses to undergo rapid adaptive mutation in cell culture, and assessed its pathogenicity in hACE2 mice. We found that the GX_P2V(short_3UTR) clone can infect hACE2 mice, with high viral loads detected in both lung and brain tissues. This infection resulted in 100% mortality in the hACE2 mice. We surmise that the cause of death may be linked to the occurrence of late brain infection». The cover of the study published on January 4 on BiorXiv before the modification on January 21, 2024 – link at the bottom of the page Then they also recall that these SARS-CoV-2, GD/2019 and GX/2017 studies were initially carried out by the well-known scientist from the Wuhan Institute of Virology: «To the best of our knowledge, this is the first report showing that a SARS-CoV-2-related pangolin coronavirus can cause 100% mortality in hACE2 mice, suggesting a risk for GX_P2V to spill over into humans. Our findings are evidently inconsistent with those of Zhengli Shiet al. (5), who tested the virulence of GX_P2V in two different hACE2 mouse models». The discussion then becomes very technical and evidence of expert biochemists or virologists: «It is important to note that we did not isolate the wild-type GX_P2V strain. The study by Zhengli Shi et al tested the GX_P2V(short_3UTR) variant that we reported. However, the adaptative evolutionary changes of this variant during their laboratory culture remain understudied. In fact, according to additional infection experiments, the uncloned GX_P2V(short_3UTR) also resulted in 100% mortality in hACE2 mice. Due to the propensity of coronaviruses to undergo adaptive mutation during passage culture, we cloned and analyzed mutations in GX_P2V(short_3UTR), focusing specifically on the pathogenicity of the cloned strains. The high pathogenicity mechanism of GX_P2V C7 in hACE2 mice, in the absence of the wild-type GX_P2V control, requires further investigation». And the conclusion doesn’t suggest anything good… «Compared to the original sequence of GX_P2V(short_3UTR), GX_P2V C7 has two amino acid mutations in the spike protein. Given the close relationship between coronavirus virulence and spike protein mutations (7), it is possible that GX_P2V C7 has undergone a virulence-enhancing mutation. However, it is important to note that our hACE2 mouse model may be relatively unique. The company has not yet published a paper on this hACE2 mouse model, but our results suggest that hACE2 may be highly expressed in the mouse brain. Additionally, according to the data provided by the company, these hACE2 mice have abnormal physiology, as indicated by relatively reduced serum triglyceride, cholesterol, and lipase levels, compared to those of wild-type C57BL/6J mice. In summary, our study provides a unique perspective on the pathogenicity of GX_P2V and offers a distinct alternative model for understanding the pathogenic mechanisms of SARS-CoV-2-related coronaviruses». The scientific explanation is cloaked by a strong emphasis on virulence which may also appear as a “threat” on the possibility of transforming these GX_P2V genotypes into a real bacteriological weapon. Fabio Giuseppe Carlo Carisio © COPYRIGHT GOSPA NEWS prohibition of reproduction without authorization follow Fabio Carisio Gospa News director on Twitter follow Gospa News on Telegram Subscribe to the Gospa News Newsletter to read the news as soon as it is published MAIN SOURCES PUBMED – Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR’ BIORXIV – Lethal Infection of Human ACE2-Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR) To receive the COMPLETE PDF OF THE ORIGINAL DISTURBING RESEARCH, subscribe to the Gospa News Newsletter and write to redazione@gospanews.net GOSPA NEWS – WUHAN-GATES DOSSIER GOSPA NEWS – COVID-19 DOSSIER Fabio G. C. Carisio Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal. His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more… Most popolar investigation on VT is: Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting. For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime. With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians. In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence. In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates His investigations was quoted also by The Gateway Pundit, Tasnim and others He worked for many years for the magazine Art & Wine as an art critic and curator. VETERANS TODAY OLD POSTS www.gospanews.net/ ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/01/terrifying-new-lethal-bio-weapon-sars-cov-3-built-and-hid-by-chinas-army/
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    Terrifying! New LETHAL BIO-WEAPON SARS-COV-3 Built and Hid by CHINA’s ARMY
    by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO The news is much more alarming than the mysterious and lethal Virus with which Bill Gates and his accomplices at the World Economic Forum have continued to threaten humanity for almost a year to push all governments to accept the Pandemic Treaty of the World Health Organization...
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  • Moderna’s influence over the US and UK governments is more than most realise
    Rhoda WilsonJanuary 3, 2024
    The sheer sprawl, corruption, influence and involvement of Moderna in politics and the wider medical industry is staggering. It is difficult to convey and harder to comprehend, The Underdog writes.

    Months before a pandemic was declared in 2020, World Economic Forum Young Global Leader and CEO of Moderna Stéphane Bancel told his staff that there was going to be a pandemic and Moderna would need to manufacture a billion doses of vaccine the “next year,” being 2021.

    How did Bancel know?

    A recent article written by The Underdog may provide some insight which lays out his/her findings relating to Moderna infiltrating the USA and UK governments as well as academia.

    The Underdog is a non de plume for someone who self-describes as a citizen journalist and publishes articles on a Substack page titled ‘The Daily Beagle’.

    In the USA, Moderna took control of the FDA and Operation Warp Speed, and influenced NIH and BARDA, The Underdog says. Adding that Moderna controls the UK government through Installed Prime Minister Rishi Sunak.

    As well as governments, The Underdog surmises that Moderna has compromised academics in universities in the USA and Canada.

    For previous articles we’ve published that relate to and complement The Underdog’s article, please see ‘Rishi Sunak, Thélème and Moderna’ and various other articles HERE.

    Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox…

    Murderous Moderna’s Infiltration of Politics

    By The Underdog

    Murder, They Wrote

    Let us clarify murderous: a peer-reviewed study found that myocarditis in under 40-year-old males was higher in those who had taken all vaccines, and those who had taken a second dose of mRNA-1273, the Moderna covid injection.

    It was so bad that Sweden, Norway, and Finland suspended the use of the Moderna vaccine in young people, as noted in the British Medical Journal (“BMJ”).

    As previously known, the US National Institutes of Health (“NIH”) and their corrupt cohorts attempted to censor evidence that myocarditis has a fatality rate of 50% within 5 years. So it isn’t unreasonable to assert Moderna has in all likelihood murdered at least 50% of those with myocarditis caused by the Moderna injections; of which will include children.

    Like in an attempt to discourage people from getting the poisonous shots without declaring that they’re harmful and recalling them, Moderna recently jacked up the price of their injections to $130. A reminder Moderna produced injections that contained stainless steel contaminants.


    It cost only $2.85 to manufacture and despite this, the US government paid $15 to $26 a dose. Why?

    Moderna Have Infiltrated the Government

    Seems pretty incredulous, but no.

    Moderna Is Part of WEF

    Stéphane Bancel was “elected” 2009 Young Global Leader by the World Economic Forum (“WEF”).


    Bancel was founding chief executive officer for Moderna and joined Flagship Pioneering in 2013.

    Noubar Afeyan, co-founder of Moderna and CEO of Flagship Pioneering, “received a Technology Pioneer 2012 award from the World Economic Forum”.

    Noubar also “served as Chairman of the Global Agenda Council on Chemicals, Advanced Materials and Biotechnology of the World Economic Forum as well as being a member of the Meta-Council on Emerging Technologies.”

    Moderna Took Control of Operation Warp Speed

    Moncef Slaoui, owning 82,508 Moderna shares on 21 February 2020, stepped down from Moderna, divested his stake, and went on to lead Operation Warp Speed. As it just so happened, the US government spent over $4 billion on Moderna, twice as much as any other pharmaceutical company:


    During this time of taking fat wads of government cash, Moderna also received heavy investment from hedge funds in September 2020.

    Moderna Influenced NIH, BARDA

    The NIH in December 2020 bragged how they worked with Moderna in a partnership, along with BARDA (Biomedical Advanced Research and Development Authority) and NIAID (National Institute of Allergy and Infectious Diseases) Vaccine Research Centre to develop the myocarditis inducing mRNA-1273 injection:

    Factoring in that the NIH deleted evidence of the myocarditis fatality rate implicating firms such as Moderna and the NIH itself, this shouldn’t be surprising.

    Moderna ultimately got into a fight with NIH over mRNA patents, with Moderna insisting they did everything. Current NIH director Francis Collins remarked the NIH played “a major role in the development of the vaccine,” in which Moderna received approximately $10 billion in government funding.

    Moderna paid the NIH their bribe patent money, to the tune of $400 million, just under half a billion, but held dispute over another patent. To try to appease the NIH, Moderna offered co-ownership of the vaccine patent with NIH.

    Curiously, an NIH employee, Philip Leder, worked on mRNA research decades before NIH’s agreement with Moderna. They conveniently died in 2020.

    Moderna Took Control of the FDA


    Stephan Hahn
    Stephen Hahn, former FDA Commissioner who insisted he’d fast-track the covid-19 injections, left the FDA to go join Flagship Pioneering after approving the injections. He claimed Donald Trump told him “to authorise a covid-19 vaccine or go.”


    Flagship Pioneering are a venture capital firm that financed and kickstarted Moderna. The CEO of Flagship Pioneering, Noubar Afeyan, also co-founded Moderna. So, they’re essentially one and the same.

    Moderna LLC was the successor in interest to Moderna Therapeutics, Inc., a Delaware corporation incorporated in 2009 as Newco LS18, Inc. by Flagship Pioneering.

    SEC EDGAR filing on Moderna LLCnone
    One of the founding investors of Moderna, Bob Langer, also previously worked on the FDA’s advisory board according to his own biography, serving as both a member and later the chairman:

    It is likely Bob retained contacts within the FDA even after leaving.

    Moderna Control the UK Government

    This isn’t hyperbole. We wish it were.

    The UK government signed a memorandum of understanding with Flagship Pioneering:

    This includes a spin-off company called Quotient Therapeutics:

    The UK government also formed an unusually aggressive and expansive 10-year contract with Moderna, worth at least £1 billion for a “new vaccine centre” – despite the fact these are genetic modification injections.


    This was agreed during Rishi Sunak’s tenure as Prime Minister.

    Moderna de facto Control the Prime Minister

    The investment will benefit current unelected pharmaceutical bureaucrat Rishi Sunak, who is the Prime Minister of the United Kingdom (read as: Moderna have influence of the UK government).


    Unelected Prime Minister Rishi Sunak
    Rishi was also formerly Chancellor of the Exchequer (read as: controlled the UK government purse strings) back in 2020, and allocated even more funds to the vaccine industry during that time. He bragged how it was a “success.” For his bank account, we surmise.

    How will he benefit? Rishi Sunak co-founded a firm called Thélème Partners LLP (aka. Thélème) back in 2009, registered in the Cayman Islands, along with co-founder and former French Navy Patrick Degorce, after they previously met at The Children’s Investment Fund (“TCIF”). TCIF was run by billionaire Chris Hohn.


    Rishi Sunak appointed Thélème partner John Sheridan as an advisor to government during his time as Chancellor of the Exchequer.

    Thélème started with an initial investment fund of £536m, and were early backers of Moderna. Thélème co-founder Degorce invested in Moderna over a decade ago, meaning their rise was also Rishi Sunak’s rise.

    Thélème are Moderna’s single largest hedge fund investor, despite Thélème cutting their exposure by 11%. On 30 September 2023, Thélème disclosed ownership of 6,897,612 shares of Moderna, Inc. (US:MRNA) valued at $712,454,343 USD, more than half a billion.

    The name Thélème is likely based upon the French ‘Abbaye de Thélème’, an idea invented by French monk Rabelais, who gives his vision of an “ideal and utopian abbey.”

    The “Thelemites of the Abbey” follow “do what thou wilt”. Occultist Aleister Crowley declared a so-called “Theleme religion” whose central belief was “do what thou wilt”, even remarking “There is no law beyond do what thou wilt.”

    Unsurprisingly, Moderna plant Rishi Sunak did whatever he wanted and declined to say that he did not profit from the Moderna injections. He claims to have left the firm in 2013 and that his finances are in a so-called “blind trust,” along with 10 other ministers. There’s no legal definition of a “blind trust” so this is pure theatre.


    Given he’s the original founder of Thélème, he no doubt has shares and investments and still stands to profit from Moderna’s success, explaining why he gave Flagship Pioneering favourable treatment and Moderna a 10-year contract on a plate. This is the same Rishi who tried to “break banks” during the 2008 collapse.

    On another note…

    Moderna Have Compromised Academia

    Bear in mind academic institutions are involved in peer-reviewed processes, clinical research and more, so this has wider, damning ramifications. Moderna were formed within the heart of academia.

    Moderna Have Control In MIT


    Noubar Afeyan
    Noubar Afeyan, CEO of Flagship Pioneering, studied at MIT (Massachusetts Institute of Technology). He was recently installed in MIT Corporation’s board of trustees.


    The purpose of the trust? (Emphasis added):

    […] to see that the Institute adheres to the purposes for which it was chartered and that its integrity and financial resources are preserved for future generations as well as for current purposes. […]

    “About the Corporation”, MIT Corporation pagenone
    Control of the finances. And integrity.

    During the founding period of Moderna, Noubar Afeyan joined the likes of MIT Bob Langer. Langer, since investing in Moderna, has now become a billionaire as a result.

    MIT Mandates the Covid-19 Injection, That MIT Based Modern Just Happens to Sell

    Profitably for MIT-inspired Moderna, during Moderna’s rise, MIT adopted a vaccine mandate, one where MIT reported there were still covid-19 cases anyway and that they weren’t mild:

    They huffed the copium and tried to argue there were no Omicron-related hospitalisations (Omicron is deemed the mildest of the covid-19 set), but conveniently omitted Alpha, Delta, and the others, implying there were other variant hospitalisations (read as: The injections they mandated for profits, didn’t work).

    Noubar Afeyan and MIT’s Bob Langer are also joined by investor Derrick Rossi (Harvard), after they learn they can reprogram human cells and reverse them back into pluripotent stem cells based on Harvard Derrick Rossi’s research. Notice it involves using mRNA to change human cells (read as: Modify their DNA).

    Rossi is head of the Harvard Department of Stem Cell and Regenerative Biology. Current Moderna CEO Stéphane Bancel also studied at Harvard.

    Rossi approached Harvard faculty member Timothy Springer asking him to invest in Moderna, which he did so. In April 2021, Timothy Springer was declared a billionaire by Cord Magazine. Back patting their own, Timothy Springer went on to receive a Lasker award, and a Robert Koch prize.

    The Koch brothers also finances MIT Bob Langer’s lab:

    In a surprise to no-one, Harvard also mandated the injection from which they stand to profit.

    This included for Harvard staff, flushing out anyone critical of the financial abuses by the vaccine industry.


    Bearing in mind the majority of Moderna directed Operation Warp Speed financing went to Moderna, the majority of the injections that would have been available would have also been primarily Moderna, guaranteeing their selfish, harmful, murderous profit

    Remember: Those below the age of 40 are adversely affected by myocarditis, and the majority of students on campus would be below that age; 50% fatality rate within 5 years for myocarditis.

    University of Toronto, As Well – Maybe Even the Canadian Government?

    The Academia orgy was apparently not big enough, and the University of Toronto wanted some, giving Derrick Rossi an “honorary degree”.


    University of Toronto are particularly interesting because they’re one of a handful of “kingmaker universities” in Canada.

    When investigating Acuitas Therapeutics, The Daily Beagle remarked:

    The only University with more Canadian Prime Ministers is University of Toronto, with Arthur Meighen, W.L. Mackenzie King, Lester B. Pearson, and Paul Martin.

    It is very likely a lot of ministers for the Canadian government also come from the University of Toronto. So, the University of Toronto’s corrupt love-in with Moderna implies Moderna also has influence over the Canadian government.

    And in surprise to no-one, the University of Toronto also anti-competitively mandated the emergency authorisation injections:


    You know, the same injections Health Canada admitted contained plasmid DNA, the same kind Moderna used in partnership with Aldevron.

    What is it with academic universities mandating the injections from which they stand to benefit financially?

    Moderna are in Bed with Multiple Major Pharmaceutical Companies

    To give you an idea how deep this shell game goes, did you know that AstraZeneca are one of the key initial investors in Moderna and a major shareholder? So it doesn’t matter to them if their AstraZeneca injection becomes the fall guy for mRNA shots – they profit either way!

    And guess what they focused on? Heart disease and cancer (any time you see the word ‘oncology’, think cancer).

    Moderna Clearly Expects a Lot of Cancer

    Moderna went batshit and agreed a lot of partnerships with major pharmaceutical firms and fired up a lot of oncology (cancer) related spin-offs.

    Even in their own timeline, they spun-off ‘Onkaido Therapeutics’ to research cancer, partnered with Merck to advocate “personalised” cancer vaccines, and then produced mRNA injections, mRNA-4157, for tumours.


    They also launched ‘Caperna LLC’, again focusing on personalised cancer vaccines.

    Flagship Pioneering (Moderna) Gets into Bed with Pfizer


    Moderna love-in Flagship Pioneering got into bed with Pfizer to do a $100 million drug discovery jaunt in July 2023. What type of drugs, they mysteriously didn’t say. Pfizer said their breakthroughs would “change patients’ lives”. They didn’t say for the better.

    This isn’t forgetting that earlier in 2023 Pfizer bought out Seagan for a whopping $43 billion in order to develop cancer drugs.


    Flagship Pioneering (Moderna) Gets into Bed With Novo Nordisk

    The target? Heart disease and “rare diseases” (it’s only “rare”):

    Established in 2022, after it was found the Moderna injections cause myocarditis. Convenient.

    The Daily Beagle Smells a Rat – Merck Again

    Despite being rightly lambasted for making a harmful, murderous product and taking a beating with stocks and shares, on about 12 December 2023, Moderna started to mysteriously climb, and The Daily Beagle smelled a rat.


    And a rat it was. On the 14 December Moderna and Merck bragged their little jaunt into personalised cancer vaccines – vaguely worded as “a powerful new cancer therapy” – was “in the works.” We wonder if it’s as “safe and effective” as the myocarditis inducing covid-19 injections.

    What a great way to profit. Introduce DNA with transfection agents that cause insertational mutagensis (read as: Cause foreign DNA to enter your DNA and cause cancer), then profit from the resulting spike in cancer cases.


    Cancer, Cancer Everywhere

    Moderna’s entire theme seems to be primarily cancer focused. Besides the partnerships with AstraZeneca, Pfizer, Merck, Novo Nordisk, Aldevron, NIH and more, it turns out Moderna is even more focused on cancer (somehow).

    Take former FDA commissioner Stephen Hahn, for example, the man who betrayed the American public for a cushy job at Flagship Pioneering:


    He specialises in oncology (cancer), having been part of the National Cancer Institute, American Association for Cancer Research, and American Society for Radiation Oncology. Conveniently this also means Moderna has influence over cancer research (read as: No investigating any Moderna-related causes of cancer).

    University of Texas Cancer Corruption

    In another tangled web of cancer-related corruption, MD Anderson Cancer Centre are owned by the Koch brothers. Koch financed the likes of Moderna’s Bob Langer’s lab and gave Moderna investor Timothy Springer a monetary award.

    MD Anderson Cancer Centre, were involved in controversy when the President, Ronald DePinho, was found to own stocks in Aveo Oncology, a company whose drugs University of Texas would be assessing in clinical trial, at none other than… the MD Anderson Cancer Centre.

    We bet it is exciting … for your bank account.

    Unsurprisingly, the corrupt University of Texas investigated itself and found itself innocent, using the meaningless term “blind trust” with zero transparency on the arrangement. University of Texas wheeled out the usual nonsense that financial conflicts of interest were somehow in the patients’ best interests.


    Surely they mean the best interests of the investors, University of Texas itself! And what safeguards? You kept the stocks and the clinical trial.

    Any Cure for The Cancer That Is Corruption?

    Apparently not.

    Even now, Moderna CEO Stéphane Bancel is somehow selling off 40,000 shares a pop via automatic sells, without somehow reducing the total number of shares he holds (???):


    Apparently Moderna can just print itself as many shares for profit as it wants, on account of how many departments and institutions it controls.

    Oh, and to top it off, Moderna are even in bed with charities. Oxfam America (you know, of Oxfam child rapists fame) filed a SEC complaint that Moderna had committed fraud and misled investors (read as: Oxfam America is an investor in Moderna).

    Tip of the Iceberg

    Phew, that’s a lot to go over. No doubt there’s more, however we’ll be cutting it here for now as it is a lot to go over. It is surprising how much influence and control Moderna have consolidated in such a short space of time, and no doubt corruption is rife abounds elsewhere too.



    https://expose-news.com/2024/01/03/modernas-influence-over-the-us-and-uk
    Moderna’s influence over the US and UK governments is more than most realise Rhoda WilsonJanuary 3, 2024 The sheer sprawl, corruption, influence and involvement of Moderna in politics and the wider medical industry is staggering. It is difficult to convey and harder to comprehend, The Underdog writes. Months before a pandemic was declared in 2020, World Economic Forum Young Global Leader and CEO of Moderna Stéphane Bancel told his staff that there was going to be a pandemic and Moderna would need to manufacture a billion doses of vaccine the “next year,” being 2021. How did Bancel know? A recent article written by The Underdog may provide some insight which lays out his/her findings relating to Moderna infiltrating the USA and UK governments as well as academia. The Underdog is a non de plume for someone who self-describes as a citizen journalist and publishes articles on a Substack page titled ‘The Daily Beagle’. In the USA, Moderna took control of the FDA and Operation Warp Speed, and influenced NIH and BARDA, The Underdog says. Adding that Moderna controls the UK government through Installed Prime Minister Rishi Sunak. As well as governments, The Underdog surmises that Moderna has compromised academics in universities in the USA and Canada. For previous articles we’ve published that relate to and complement The Underdog’s article, please see ‘Rishi Sunak, Thélème and Moderna’ and various other articles HERE. Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… Murderous Moderna’s Infiltration of Politics By The Underdog Murder, They Wrote Let us clarify murderous: a peer-reviewed study found that myocarditis in under 40-year-old males was higher in those who had taken all vaccines, and those who had taken a second dose of mRNA-1273, the Moderna covid injection. It was so bad that Sweden, Norway, and Finland suspended the use of the Moderna vaccine in young people, as noted in the British Medical Journal (“BMJ”). As previously known, the US National Institutes of Health (“NIH”) and their corrupt cohorts attempted to censor evidence that myocarditis has a fatality rate of 50% within 5 years. So it isn’t unreasonable to assert Moderna has in all likelihood murdered at least 50% of those with myocarditis caused by the Moderna injections; of which will include children. Like in an attempt to discourage people from getting the poisonous shots without declaring that they’re harmful and recalling them, Moderna recently jacked up the price of their injections to $130. A reminder Moderna produced injections that contained stainless steel contaminants. It cost only $2.85 to manufacture and despite this, the US government paid $15 to $26 a dose. Why? Moderna Have Infiltrated the Government Seems pretty incredulous, but no. Moderna Is Part of WEF Stéphane Bancel was “elected” 2009 Young Global Leader by the World Economic Forum (“WEF”). Bancel was founding chief executive officer for Moderna and joined Flagship Pioneering in 2013. Noubar Afeyan, co-founder of Moderna and CEO of Flagship Pioneering, “received a Technology Pioneer 2012 award from the World Economic Forum”. Noubar also “served as Chairman of the Global Agenda Council on Chemicals, Advanced Materials and Biotechnology of the World Economic Forum as well as being a member of the Meta-Council on Emerging Technologies.” Moderna Took Control of Operation Warp Speed Moncef Slaoui, owning 82,508 Moderna shares on 21 February 2020, stepped down from Moderna, divested his stake, and went on to lead Operation Warp Speed. As it just so happened, the US government spent over $4 billion on Moderna, twice as much as any other pharmaceutical company: During this time of taking fat wads of government cash, Moderna also received heavy investment from hedge funds in September 2020. Moderna Influenced NIH, BARDA The NIH in December 2020 bragged how they worked with Moderna in a partnership, along with BARDA (Biomedical Advanced Research and Development Authority) and NIAID (National Institute of Allergy and Infectious Diseases) Vaccine Research Centre to develop the myocarditis inducing mRNA-1273 injection: Factoring in that the NIH deleted evidence of the myocarditis fatality rate implicating firms such as Moderna and the NIH itself, this shouldn’t be surprising. Moderna ultimately got into a fight with NIH over mRNA patents, with Moderna insisting they did everything. Current NIH director Francis Collins remarked the NIH played “a major role in the development of the vaccine,” in which Moderna received approximately $10 billion in government funding. Moderna paid the NIH their bribe patent money, to the tune of $400 million, just under half a billion, but held dispute over another patent. To try to appease the NIH, Moderna offered co-ownership of the vaccine patent with NIH. Curiously, an NIH employee, Philip Leder, worked on mRNA research decades before NIH’s agreement with Moderna. They conveniently died in 2020. Moderna Took Control of the FDA Stephan Hahn Stephen Hahn, former FDA Commissioner who insisted he’d fast-track the covid-19 injections, left the FDA to go join Flagship Pioneering after approving the injections. He claimed Donald Trump told him “to authorise a covid-19 vaccine or go.” Flagship Pioneering are a venture capital firm that financed and kickstarted Moderna. The CEO of Flagship Pioneering, Noubar Afeyan, also co-founded Moderna. So, they’re essentially one and the same. Moderna LLC was the successor in interest to Moderna Therapeutics, Inc., a Delaware corporation incorporated in 2009 as Newco LS18, Inc. by Flagship Pioneering. SEC EDGAR filing on Moderna LLCnone One of the founding investors of Moderna, Bob Langer, also previously worked on the FDA’s advisory board according to his own biography, serving as both a member and later the chairman: It is likely Bob retained contacts within the FDA even after leaving. Moderna Control the UK Government This isn’t hyperbole. We wish it were. The UK government signed a memorandum of understanding with Flagship Pioneering: This includes a spin-off company called Quotient Therapeutics: The UK government also formed an unusually aggressive and expansive 10-year contract with Moderna, worth at least £1 billion for a “new vaccine centre” – despite the fact these are genetic modification injections. This was agreed during Rishi Sunak’s tenure as Prime Minister. Moderna de facto Control the Prime Minister The investment will benefit current unelected pharmaceutical bureaucrat Rishi Sunak, who is the Prime Minister of the United Kingdom (read as: Moderna have influence of the UK government). Unelected Prime Minister Rishi Sunak Rishi was also formerly Chancellor of the Exchequer (read as: controlled the UK government purse strings) back in 2020, and allocated even more funds to the vaccine industry during that time. He bragged how it was a “success.” For his bank account, we surmise. How will he benefit? Rishi Sunak co-founded a firm called Thélème Partners LLP (aka. Thélème) back in 2009, registered in the Cayman Islands, along with co-founder and former French Navy Patrick Degorce, after they previously met at The Children’s Investment Fund (“TCIF”). TCIF was run by billionaire Chris Hohn. Rishi Sunak appointed Thélème partner John Sheridan as an advisor to government during his time as Chancellor of the Exchequer. Thélème started with an initial investment fund of £536m, and were early backers of Moderna. Thélème co-founder Degorce invested in Moderna over a decade ago, meaning their rise was also Rishi Sunak’s rise. Thélème are Moderna’s single largest hedge fund investor, despite Thélème cutting their exposure by 11%. On 30 September 2023, Thélème disclosed ownership of 6,897,612 shares of Moderna, Inc. (US:MRNA) valued at $712,454,343 USD, more than half a billion. The name Thélème is likely based upon the French ‘Abbaye de Thélème’, an idea invented by French monk Rabelais, who gives his vision of an “ideal and utopian abbey.” The “Thelemites of the Abbey” follow “do what thou wilt”. Occultist Aleister Crowley declared a so-called “Theleme religion” whose central belief was “do what thou wilt”, even remarking “There is no law beyond do what thou wilt.” Unsurprisingly, Moderna plant Rishi Sunak did whatever he wanted and declined to say that he did not profit from the Moderna injections. He claims to have left the firm in 2013 and that his finances are in a so-called “blind trust,” along with 10 other ministers. There’s no legal definition of a “blind trust” so this is pure theatre. Given he’s the original founder of Thélème, he no doubt has shares and investments and still stands to profit from Moderna’s success, explaining why he gave Flagship Pioneering favourable treatment and Moderna a 10-year contract on a plate. This is the same Rishi who tried to “break banks” during the 2008 collapse. On another note… Moderna Have Compromised Academia Bear in mind academic institutions are involved in peer-reviewed processes, clinical research and more, so this has wider, damning ramifications. Moderna were formed within the heart of academia. Moderna Have Control In MIT Noubar Afeyan Noubar Afeyan, CEO of Flagship Pioneering, studied at MIT (Massachusetts Institute of Technology). He was recently installed in MIT Corporation’s board of trustees. The purpose of the trust? (Emphasis added): […] to see that the Institute adheres to the purposes for which it was chartered and that its integrity and financial resources are preserved for future generations as well as for current purposes. […] “About the Corporation”, MIT Corporation pagenone Control of the finances. And integrity. During the founding period of Moderna, Noubar Afeyan joined the likes of MIT Bob Langer. Langer, since investing in Moderna, has now become a billionaire as a result. MIT Mandates the Covid-19 Injection, That MIT Based Modern Just Happens to Sell Profitably for MIT-inspired Moderna, during Moderna’s rise, MIT adopted a vaccine mandate, one where MIT reported there were still covid-19 cases anyway and that they weren’t mild: They huffed the copium and tried to argue there were no Omicron-related hospitalisations (Omicron is deemed the mildest of the covid-19 set), but conveniently omitted Alpha, Delta, and the others, implying there were other variant hospitalisations (read as: The injections they mandated for profits, didn’t work). Noubar Afeyan and MIT’s Bob Langer are also joined by investor Derrick Rossi (Harvard), after they learn they can reprogram human cells and reverse them back into pluripotent stem cells based on Harvard Derrick Rossi’s research. Notice it involves using mRNA to change human cells (read as: Modify their DNA). Rossi is head of the Harvard Department of Stem Cell and Regenerative Biology. Current Moderna CEO Stéphane Bancel also studied at Harvard. Rossi approached Harvard faculty member Timothy Springer asking him to invest in Moderna, which he did so. In April 2021, Timothy Springer was declared a billionaire by Cord Magazine. Back patting their own, Timothy Springer went on to receive a Lasker award, and a Robert Koch prize. The Koch brothers also finances MIT Bob Langer’s lab: In a surprise to no-one, Harvard also mandated the injection from which they stand to profit. This included for Harvard staff, flushing out anyone critical of the financial abuses by the vaccine industry. Bearing in mind the majority of Moderna directed Operation Warp Speed financing went to Moderna, the majority of the injections that would have been available would have also been primarily Moderna, guaranteeing their selfish, harmful, murderous profit Remember: Those below the age of 40 are adversely affected by myocarditis, and the majority of students on campus would be below that age; 50% fatality rate within 5 years for myocarditis. University of Toronto, As Well – Maybe Even the Canadian Government? The Academia orgy was apparently not big enough, and the University of Toronto wanted some, giving Derrick Rossi an “honorary degree”. University of Toronto are particularly interesting because they’re one of a handful of “kingmaker universities” in Canada. When investigating Acuitas Therapeutics, The Daily Beagle remarked: The only University with more Canadian Prime Ministers is University of Toronto, with Arthur Meighen, W.L. Mackenzie King, Lester B. Pearson, and Paul Martin. It is very likely a lot of ministers for the Canadian government also come from the University of Toronto. So, the University of Toronto’s corrupt love-in with Moderna implies Moderna also has influence over the Canadian government. And in surprise to no-one, the University of Toronto also anti-competitively mandated the emergency authorisation injections: You know, the same injections Health Canada admitted contained plasmid DNA, the same kind Moderna used in partnership with Aldevron. What is it with academic universities mandating the injections from which they stand to benefit financially? Moderna are in Bed with Multiple Major Pharmaceutical Companies To give you an idea how deep this shell game goes, did you know that AstraZeneca are one of the key initial investors in Moderna and a major shareholder? So it doesn’t matter to them if their AstraZeneca injection becomes the fall guy for mRNA shots – they profit either way! And guess what they focused on? Heart disease and cancer (any time you see the word ‘oncology’, think cancer). Moderna Clearly Expects a Lot of Cancer Moderna went batshit and agreed a lot of partnerships with major pharmaceutical firms and fired up a lot of oncology (cancer) related spin-offs. Even in their own timeline, they spun-off ‘Onkaido Therapeutics’ to research cancer, partnered with Merck to advocate “personalised” cancer vaccines, and then produced mRNA injections, mRNA-4157, for tumours. They also launched ‘Caperna LLC’, again focusing on personalised cancer vaccines. Flagship Pioneering (Moderna) Gets into Bed with Pfizer Moderna love-in Flagship Pioneering got into bed with Pfizer to do a $100 million drug discovery jaunt in July 2023. What type of drugs, they mysteriously didn’t say. Pfizer said their breakthroughs would “change patients’ lives”. They didn’t say for the better. This isn’t forgetting that earlier in 2023 Pfizer bought out Seagan for a whopping $43 billion in order to develop cancer drugs. Flagship Pioneering (Moderna) Gets into Bed With Novo Nordisk The target? Heart disease and “rare diseases” (it’s only “rare”): Established in 2022, after it was found the Moderna injections cause myocarditis. Convenient. The Daily Beagle Smells a Rat – Merck Again Despite being rightly lambasted for making a harmful, murderous product and taking a beating with stocks and shares, on about 12 December 2023, Moderna started to mysteriously climb, and The Daily Beagle smelled a rat. And a rat it was. On the 14 December Moderna and Merck bragged their little jaunt into personalised cancer vaccines – vaguely worded as “a powerful new cancer therapy” – was “in the works.” We wonder if it’s as “safe and effective” as the myocarditis inducing covid-19 injections. What a great way to profit. Introduce DNA with transfection agents that cause insertational mutagensis (read as: Cause foreign DNA to enter your DNA and cause cancer), then profit from the resulting spike in cancer cases. Cancer, Cancer Everywhere Moderna’s entire theme seems to be primarily cancer focused. Besides the partnerships with AstraZeneca, Pfizer, Merck, Novo Nordisk, Aldevron, NIH and more, it turns out Moderna is even more focused on cancer (somehow). Take former FDA commissioner Stephen Hahn, for example, the man who betrayed the American public for a cushy job at Flagship Pioneering: He specialises in oncology (cancer), having been part of the National Cancer Institute, American Association for Cancer Research, and American Society for Radiation Oncology. Conveniently this also means Moderna has influence over cancer research (read as: No investigating any Moderna-related causes of cancer). University of Texas Cancer Corruption In another tangled web of cancer-related corruption, MD Anderson Cancer Centre are owned by the Koch brothers. Koch financed the likes of Moderna’s Bob Langer’s lab and gave Moderna investor Timothy Springer a monetary award. MD Anderson Cancer Centre, were involved in controversy when the President, Ronald DePinho, was found to own stocks in Aveo Oncology, a company whose drugs University of Texas would be assessing in clinical trial, at none other than… the MD Anderson Cancer Centre. We bet it is exciting … for your bank account. Unsurprisingly, the corrupt University of Texas investigated itself and found itself innocent, using the meaningless term “blind trust” with zero transparency on the arrangement. University of Texas wheeled out the usual nonsense that financial conflicts of interest were somehow in the patients’ best interests. Surely they mean the best interests of the investors, University of Texas itself! And what safeguards? You kept the stocks and the clinical trial. Any Cure for The Cancer That Is Corruption? Apparently not. Even now, Moderna CEO Stéphane Bancel is somehow selling off 40,000 shares a pop via automatic sells, without somehow reducing the total number of shares he holds (???): Apparently Moderna can just print itself as many shares for profit as it wants, on account of how many departments and institutions it controls. Oh, and to top it off, Moderna are even in bed with charities. Oxfam America (you know, of Oxfam child rapists fame) filed a SEC complaint that Moderna had committed fraud and misled investors (read as: Oxfam America is an investor in Moderna). Tip of the Iceberg Phew, that’s a lot to go over. No doubt there’s more, however we’ll be cutting it here for now as it is a lot to go over. It is surprising how much influence and control Moderna have consolidated in such a short space of time, and no doubt corruption is rife abounds elsewhere too. https://expose-news.com/2024/01/03/modernas-influence-over-the-us-and-uk
    EXPOSE-NEWS.COM
    Moderna’s influence over the US and UK governments is more than most realise
    The sheer sprawl, corruption, influence and involvement of Moderna in politics and the wider medical industry is staggering. It is difficult to convey and harder to comprehend, The Underdog writes.…
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