By Dr. Ariyana Love

Covid-19 is a biological and technological weapon system using self-replicating, programmable nanotechnology with synthetic modRNA poisons. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” because that’s medical science. 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.”

The first Anthrax was a biological weapon developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene“ into the highly toxic Bacillus Anthracis bacteria. This means that advanced technologies such as Cross-Species-Genomics capability was acquired by the government before 1950 when a lethal bacteria 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. Being the bioweapon of choice, NIH funded Anthony Fauci increased Anthrax’s lethality. Russia’s Anthrax was genetically attenuated by the NIH 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” Democide.


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”. Both have just been administered to the world population through inoculations, PCR swabs and aerosolization and self-replication.

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, also 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 admits to 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 of 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.

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

Here’s how they did it. 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 it from replicating inside the human body 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 mosquitoes 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’s 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.”

In layman’s terms, the poisonous Anthrax “antigen” is being used in the genetic modification of the human genome and it’s literally being encoded into the genome, after knockouts (deletions) of the genome.

The molecular basis of Anthrax “vaccines” contains “spores and DNA plasmids.“ This is a targeted weapon system. 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.

Luciferase is insect DNA and that’s going into the genome. 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 (aerosolization), 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

The 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.

According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is Alhydrogel. The Alhydrogel is infused with 750 μg of aluminum, making it magnetic. In the Alhydrogel invention, Anthrax was fused together into this nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”.

Again 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.

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, which is what I believe some eugenicists were trying to achieve.

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

This Alhydrogel patent demonstrates its 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.

It begs the question, where do venereal diseases come from? But I digress.

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 however, 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.

So, both nanoparticles and Anthrax have been used in vaccines for decades already, without 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.

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 swabs which contain delayed release technology that contains a military weapon system.

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.

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.


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


They also say the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a complete disaster. U.S. Army statistics that were never published show the Anthrax “vaccine” induces cancers.

The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis? Anthrax also coagulates the blood. Read more here and here.

“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.”

Anthrax also causes a person to hemorrhage. So this explains all the excessive bleeding people experience after Covid-19 injections and from aerosolized exposure. In other words, shedding by transmission. Inhalation Anthrax.

Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by https://pmc.ncbi.nlm.nih.gov/articles/PMC3124019/proinflammatory cytokine signaling and histological lesions in the spleen.

Anthrax has been tested on the public already. During 9/11 Anthrax spores were intentionally released into “some environments” in NYC, 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 on with Injection Anthrax.

Our skies are sprayed with smart dust and chemicals daily. Our governments have launched 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 Whole 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 and other severe symptoms, 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. If you have been exposed to Inhalation Anthrax, you will feel hot and very flushed, similar 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 a good doctor with complete protocols.

I have been successfully detoxing people from the Covid-19 bioweapons for two years. I have a complete protocol for Anthrax poisoning. If you would like to schedule a consultation with me, please do so through my online booking system.

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

by Dr. Ariyana Love, ND

The samples pulled out of the veins and arteries of COVID vaxxed corpses shocked the world and exposed that something more than just “vaccination” is taking place.

In my latest interview with Stew Peters entitled, Human Umbilical Cord Being Injected In Kids: Tissue Scaffolding Technology In Covid Jab, I revealed in detail what the strange “blood clot” samples found by embalmer Richard Herschman, actually are. The story was first aired by Dr. Jane Ruby on Stew Peters Show in January and was recently examined LIVE on air by scientist Mike Adams in the InfoWars studio, in a worldwide medical bombshell.

The samples pulled out of the veins and arteries of COVID vaccinated corpses shocked the world and exposed that something more than just “vaccination” is happening with the COVID vaxx. The fact that mainstream media did not pick up on this story is more proof we’re in dystopian times.

Embalmer Richard Heirschman’s samples published by Dr. Jane Ruby
Embalmer Richard Herischman’s sample published by Mike Adams of Natural News

These images show synthetic tissue is being grown inside humans from the COVID vaxx. This is most likely the cause of “Sudden Adult Death Syndrome.”

Please see the following studies:

Tissue-Engineered Blood Vessels (2005)
Researchers Grow New Blood Vessels In Just Seven Days (2014)
Arterial reconstruction with human bioengineered acellular blood vessels in patients with peripheral arterial disease
From Autologous Flaps to Engineered Vascularized Grafts for Bone Regeneration

China constructing blood vessels (2020)

Bioactive polymeric scaffolds for tissue engineering

Below are images of artificially grown blood vessels by lab scientists.

Artificial blood vessels
Artificial blood vessels

There are synthetic and natural polymers. They are elastic and made from these five different materials:

  1. Polyester polymers PLLA and PGA are among the most commonly used biodegradable synthetic polymers.
  1. Silk fibroin protein is extruded from insects and worms. It has biocompatible properties with the human body and ossess relatively high tensile strength.
  1. Collagenis used for bone construction.
  1. Hyaluronic acid (HA) is a form of hydrogel material for both hard and soft tissue construction.
  1. Chitosan is biodegradable polysaccharide that comes from chitin via chemical hydrolysis. It’s used in a gel, sponge, or fiber form.

I believe the below image from the embalmer and published by InfoWars, is a Silk fibroin tissue construct.

Certified embalmer Richard Hirschman’s sample – infoWars

NANOWIRES

Nanowires are being used for the hybridization of humans. Pharmaceutical companies and world governments are attempting to grow artificial tissue inside humans, using organic matter from cross-species genomics. They appear to be trying to merge humans with electronic devices for internal tracking and remote control.

Nanowires are superconducter batteries used for tissue scaffolding inside the human body. I wrote about tissue scaffolding technology in December of 2021, in my article entitled, Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State.

See studies and patent examples:

Nanowires

Nanowire arrays for neurotechnology and other applications

Internalization of ferromagnetic nanowires by different living cells (2010)

Hydrophobic copper nanowires for enhancing condensation heat transfer

Rotational Maneuver of Ferromagnetic Nanowires for Cell Manipulation

Internalization of ferromagnetic nanowires by different living cells

Ultrathin gold nanowires to enhance radiation therapy

The presence of gold nanowires cause elevated lipid peroxidation and intracellular oxidative stress under radiation. This can literally fry people from the inside using microwave frequency. This could explain why vaxxed persons are reporting torture by electrical activity in their head and their body.

I believe the image below that was shared by Mike Adams on InfoWars, shows a gold Nanowire.

Gold Nanowire – InfoWars

This study entitled, Macroporous nanowire nanoelectronic scaffolds for synthetic tissues, reveals electrical sensors made from silicon which are lab-on-a-chip pharmacological platforms and hybrid 3D electronics-tissue materials for synthetic biology and tissue construction for inside the human body. These are planar devices used to probe electrical activity near the surface of the heart, brain and skin, acting as transmitters, transistor and receivers.

“This is nanoelectronics throughout biomaterials and synthetic tissues in 3D using macroporous nanoelectronic scaffolds. They are using silicon nanowire field effect transistor (FET)-based nanoelectronic biomaterials, given their capability for recording both extracellular and intracellular signals with subcellular resolution.”

Nanowires are also called detectors, metal electrode or carbon nanotube/nanofiber or NanoES. They are implantable microelectrodes, nanoscale semiconductors and flexible/stretchable electrodes. The sensor network is flecible, macroporous and 3D. They are used to construct artificial tissue with embedded nanoelectric sensory capabilities.

Below is an image of Nanowires.

Nanowires

ORGANOIDS

Organoids are used to construct a new brain inside humans, for mind control. Organoids and transgenic hydras are being used to build a new neural network inside the body. The studies showing this can be found in my article entitled, Pharma Exposed! Autism Spectrum Disorder (ASD) Is Targeted Gene Deletion!

Also see: Transgenic Hydras & Parasites A Biological Weapons System For Rapid HumanCloning.

MICROSPHERES

I wrote about Microspheres, Microbubbles and Microbeads delayed release technology in my article entitled, Quantum Dots, DNA Barcoding, Nano-Razors & The IsraeliState.

Microspheres are in the COVID shots. They are also used for tissue engineering and scaffolding, simultaneous drug delivery and for growing cells inside the human body. The technology is externally controlled by EMF transmission. Microspheres can release their payload, weeks, months and even years later.

This tech was developed with the purpose of destroying cancerous tumor cells and now it’s being misused for the Democide of humanity.

The study entitled, Nanostructured injectable cell microcarriers for tissue regeneration, demonstrates that nanostructured microspheres include nanocomposite and nanofibrous microspheres which have been employed as cell carriers for tissue construction. They produce cell attachment and growth, promote cell-carrier interactions and facilitate stem cell differentiation for target tissue construction inside the human body.

A study entitled, PHBV Microspheres as Tissue Engineering Scaffold for Neurons, demonstrates that Polymeric microspheres are being used to grow artificial neurons inside humans.

A study entitled, Breathing life into engineered tissues using oxygen-releasing biomaterials reveals that the artificial cells feeds on your blood to grow and survive! This may explain the strange blood clots we’re seeing in vaxxed injured persons. Human umbilical vein endothelial cells are used to grow the artificial cells.

This study entitled, Generation and differentiation of microtissues from multipotent precurser cells for use in tissue engineering, reveals that Microspheres use unrestricted somatic stem cells from human umbilical cord blood.

This technology is truly vampiric and relies on human baby tissue in order to be grown inside humans. This should not be injected into anyone, especially not children!

——————————————————————————————————

Daniel 2:43 (KJV)

(43) And whereas thou sawest iron mixed with miry clay, they shall mingle themselves with the seed of men: but they shall not cleave one to another, even as iron is not mixed with clay.

By Dr. Ariyana Love, N.D.

In a recent interview with Maria Zeee on Zeee Media, I discussed another very troubling discovery about the mRNA bioweapons technology. Maria Zeee asked me to shed more light on the Doherty Institutes involvement with the US biolabs in Ukraine.

Russian reports revealed that 350 cryocontainers with blood serum samples were transferred from the Public Health Centre of the Ministry of Health of Ukraine to a reference laboratory for infectious diseases at the Doherty Institute in Australia.

Under the guise of tackling Placental Malaria, the Doherty Institute has been directly involved in research using insects such as mosquitos and tics as bioweapons carriers. The Doherty Institute also developed a “vaccine” that uses a parasite to target the placenta of pregnant women to abort their babies in utero, under the pretext of “antibody research”.

During the testing of this novel technology, mosquitos were developed as carriers of a genetically attenuated parasite called the P. falciparum which is the most deadly of the 5 Malaria causing parasites. The World Health Organization (WHO) and the U.S. Government were also directly involved in this research to “immunize” via mosquito bite using radiation-attenuated Sporozoites.

In May of 2021, a Bill Gates-funded firm began releasing genetically modified mosquitoes in the wild.

Clinical trials conducted by the WHO in 2020, used 11 human volunteers who were “immunized” with more than 1000 bites by irradiated mosquitos infected by Sporozoites (Spz) from the P. falciparum NF54 strain or 3D7/NF54 clone.

The female Anopheles mosquito inject a minimum of Sporozoites (Spz) (~ 100) during its bite. It was tested on adolescents, children and infants aged 6 months old. 1 out of the 6 volunteers developed parasitaemia 12 days after exposure. Parasitaemia means parasites in the blood.

The parasite “vaccines” use radiation-attenuated Sporozoite, administered under drug coverage. Genetically-attenuated Sporozoite “vaccines” and recombinant protein “vaccines” (RTS,S and R21) and recombinant viral vectors “vaccines” (Chad63 MVA ME-TRAP, CSVAC, ChAd63 METRAP and MVA METRAP with the matrix-M adjuvant) are all used.

Sporozoite recombinant proteins, DNA or viral vectored protein fragments (mRNA) and attenuated Sporozoite “vaccines” induce malaria reactive CD4+ and CD8+ T-lymphocyte counts. Radiation-attenuated Sporozoite (RAS), genetically-attenuated parasite (GAP) and Sporozoite are administered under drug coverage, according to the WHO study. Here’s another WHO study from 2021.

By 2021, they had a P. falciparum Sporozoite (PfSPZ) “vaccine” as the main candidate containing live, radiation-attenuated, whole, aseptic and metabolically active Sporozoite which have been isolated from the salivary glands of mosquitos infected by P. falciparum. They tested their novel “vaccine” on infants in Kenya.

Another study conducted by the NIAID in 2022, used Malian children 6-10 years old and injected them with three doses of the PfSpz “vaccine” to induce an “infection” by “parasitic disease” of a “vector borne disease” using the P. falciparum.

Another study in 2021 carried out by the U.S. Government, experimented on 336 infants aged 5-12 months, in Kenya, inoculating them with the P. falciparum “vaccine”. This is not in fact a “vaccine” but a weapons system for the murder of babies in utero and this is a bioweapon which is transmissible to others, according to the WHO research.

In addition, the WHO’s P. falciparum research helped in the development of monoclonal antibodies. In fact, the P. falciparum parasite is a critical component in the monoclonal antibodies bioweapon system.

Please also see: Monoclonal Antibodies Is Experimental Gene Therapy – PatentReview

PATENT

The PRIMVAC “vaccine” candidate was in government trials in 2016. By 2020, the PRIMVAC “vaccine” adjuvanted with Alhydrogel was in clinical trials. The Alhydrogel patent shows unsafe levels of aluminum and other heavy metals.

A VAR2CSA plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) patent for a synthetic protein was registered in December, 2014. The VAR2CSA “vaccine” is owned by the U.S. Government.

The CDC is also involved in this VAR2CSA bioweapons development.

STERILIZATION OF THE NATIONS

Children’s Health Defence reported in August that the Covid-19 injections are dangerous for mothers and babies. According to former Chief Scientist of Pfizer, Dr. Mike Yeadon, the injected ingredients is building up in the ovaries and attacking the placenta of pregnant women.

A preliminary findings of mRNA Covid-19 vaccine safety in pregnant persons found that 4 out of 5 pregnant women are loosing their unborn baby to spontaneous abortions.

A recent report released in March of this year, shows that fetal deaths due to “covid vaccines” are almost 2,000% greater than deaths associated with other vaccines.

Below are a few highlights from the WHO study Plasmodium falciparum pre-erythrocytic stage vaccine development that I want to draw your attention to.

RECOMBINANT VIRAL VECTOR “VACCINES”

“Viral vectors represent promising tools for vaccine development, because they enable intracellular antigens to be expressed by increasing the ability to generate robust cytotoxic T-lymphocyte responses and proinflammatory interferon and cytokine production without the need for an adjuvant. However, there is great concern regarding their genotoxicity due to possible viral genome integration; this has led to many efforts aimed at finding a high level of safety and efficacy.”

Several viral, bacterial, and parasite vectors have been used in anti-malarial vaccine candidates; currently, many clinical trials are exploring their advantages to increase their potential and accelerate their use in vaccines.”

CHAD63 MVA ME-TRAP

“This anti-malarial vaccine was developed using chimpanzee adenovirus 63 (Chad63) and modified Vaccinia virus Ankara (MVA) into which were inserted genes encoding the thrombospondin-related adhesion protein (TRAP) multiple epitope (ME) chain.”

“The ME-TRAP hybrid is thus a 2398 base pair (bp) insert encoding a single 789 aa-long peptide, covering the complete P. falciparum TRAP sequence, fused to a chain of 20 malaria T- and B-cell epitopes (14 targeting MHC class I, 3 MHC class II and 1 murine).”

PCR

“A trial involving adults in Senegal to assess vaccine efficacy using a polymerase chain reaction (PCR) assay was able to detect > 10 parasites/μl blood. PCR was positive for 12 out of 57 participants vaccinated with ChAd63 ME-TRAP with a booster dose of MVA ME-TRAP and 13 out of 58 control patients who received an anti-rabies vaccine were positive by PCR, giving 8% efficacy (which was not statistically significant). They thus grouped the results with the 67% efficacy obtained in a study in Kenya and, using Cox regression, showed 50% overall vaccine efficacy in both populations.”

CSVAC

“CSVAC, a vaccine from Chad63 and MVA to encode the P. falciparum CS protein, continued such line of research into plasmid DNA anti-malarial vaccines; the CS insert was a codon-optimized cDNA encoding the CS protein truncated at the C-terminal extreme thereby lacking 14 C-terminal aa and thus omitting the GPI anchor.”

FUTURE DIRECTIONS

“Nanovaccinology” with Self-Assembling Protein Nanoparticles (SAPNs)… The next major challenge concerns the host’s genetic variability and parasite proteins’ interaction with the human immune system.”

“The choice of antigen to be used is quite complicated due to factors such as the parasite’s complex life-cycle involving two reproduction cycles (sexual and asexual), different development stages and two hosts (the Anopheles mosquito and human beings). All this can be added to the multiple invasion routes described so far for each of its target cells (hepatocytes and/or erythrocytes), the parasite’s ability to modify its gene expression and the genetic variability between P. falciparum circulating strains.”

“The next major challenge concerns the host’s genetic variability, particularly major histocompatibility class II (MHCII) complex molecules exerting their mechanism by synthesizing proteins encoded by the HLA-DR regions β1*, β3*, β4* and β5* where the HLA-DR β1* region encodes more than 1500 genetic variants grouped into 16 allele families called HLA-DRβ1*01, *03, *04, *07, etc. Parasite proteins’ interaction with the human immune system should be analysed by predicting B and T epitopes (using NetMHCIIpan 3.2 or other predictors).”

UPDATE: 6/6/2022

Please see: Pfizer’s mRNA Vaccine Goes Into Liver Cells and Is Converted to DNA: Study

By Dr. Ariyana Love, N.D.

Intro:

In March, I joined Stew Peters Show for a couple of interviews, to provide insight into Putin’s purging of bioweapons labs in Ukraine. Those interviews went viral.

First interview: Putin’s Secret War: Ukrainian Bioweapon Labs Exposed

Second interview: Horrifying Russian Report: Ukrainian Biolabs Creating Special Bioweapons For Ethnic Cleansing

This article is to provide supporting evidence, links and documents for further study.

GENETIC WARFARE

Russia’s military operation in Ukraine is entirely justified and in accordance with international law. The US Government, DOD and NATO partners were funding and operating 30 Ukrainian bioweapons labs under a “Covid-19 prevention program” but in actuality, they were producing chimeric pathogens for the “vaccine” Holocaust.

The US has admitted to the bioweapons labs but is desperately trying to destroy and hide the evidence that they violated Article 1 of the Biological and Toxic Weapons Convention of 1973. The UN is participating in the cover-up by rebranding the bioweapons facilities as “Public Health laboratories”.

The same corrupt media trickery and propaganda is being used today by the cabal, to black PR Russia/Putin and create a false narrative that spins confusion and drives division among people. It was no different during Putin’s intervention in Syria.

Moscow reports that Hunter Biden helped finance a US military ‘bioweapons’ research program in Ukraine. Hunter’s laptop emails provide the supporting evidence that he did in fact help secure millions in funding for US contractor in Ukraine, specializing in deadly pathogen research.

145 species of bioweapons have been developed in Ukraine in violation of international law and two of them were crossing into Russia. The cabal had used biological weapons in an act of war against not only Russia, but the entire world.

Routes into Europe were also being mapped. Parasites and insects that carry chimeric pathogens to infect Humans with, were being smuggled out of Ukraine and the bio-samples were being transferred abroad.

Classified documents captured by Russia reveal a paper trail between Ukrainian biolabs and the Doherty Institute in Australia. Victorian Infectious Diseases Laboratory in Melbourne was caught importing blood serum from Ukrainian biolabs. There’s 350 cryocontainers with samples of blood at the Australian Institute that are being used under the pretense of “antibody research”.

Aussie Cossak reported that Australian mercenaries have been spotted in Ukraine, in the city of Zhitomir, 150km West of Kiev.

Russia also revealed that the U.S. biolabs in Ukraine created genetic bioweapons to target certain ethnic groups for race-specific ethnic cleansing. A scientific study published in December of 2021, shows that Europeans are the most targeted ethnic group while Ashkenazi Jews (Khazars) are entirely immune to any genetic modification. Now this is some damning evidence.

Now the DNA harvesting PCR Kits under the guise of “covid testing” should make a lot more sense to you. Your DNA is so valuable to them.

BACKGROUND

George Soros has been controlling Ukraine since 2012 and stealing the regions natural resources.

Former President Barack Obama himself authorized the construction of the biolabs in Ukraine for creating dangerous pathogens, in 2005. It was the Obama/Biden deep state regime established a coup d’etat rule in Kiev, together with the Israeli state.

Jewish oligarch billionaires in Ukraine with dual nationality to Israel, such as Igor Kolomoisky, funded the neo-Nazi Azov Battalion while the Israeli state armed them.

Former US Marine Corp Intelligence Officer Scott Ritter told George Galloway “The first troops to be trained by US and British soldiers were the neo-Nazi Azov Battalion”.

The Azov Nazi’s officially integrated into the National Guard of Ukraine in 2014. Azov violently overthrew the legitimate president of Ukraine and forced their way into the government. The newer Zelensky’s puppet regime has been using internationally banned cluster bombs and other bombs against civilians, according to a Human Rights Watch reports, while the militarized Azov Nazi’s have been committing war crimes atrocities against Russian-Christian Ukrainians, especially in Eastern Ukraine. Investigative Journalist Laura Logan confirms there are mass graves in Ukraine from Zelensky’s regime.

In October 2019, Congress wrote U.S. Secretary Mike Pompeo, asking why the State Department failed to include the Azov Battalion on the Foreign Terrorist Organization list.

Israeli news Haaretz reported that the Jewish oligarchs will now flee to Israel where they will be given indemnity from their crimes against humanity.

H5N1 & H1N1

The US Department of State was able to control everything that happened within the Ukrainian biolabs. Tucker Carlson reported that the U.S. Government released a document in 2020 admitting that the bioweapons facilities in Ukraine are for “vaccine development”.

The Russian military discovered the plague, anthrax, tularemia, cholera, Ebola, Filoviruses’ and more, were being developed in Ukraine. Ebola is used in the J&J and Sinovax gene editing weaponry while the Filovirus is used in Moderna. Biotech companies are clearly getting their Gain-of-Function pathogens from Ukraine.

Russia also mentioned that the H5N1 and H1N1 are being produced in the U.S. biolabs. H1N1 induces Smallpox.

Israeli Mossad Microbiologist Joseph Moshe tried to warn the public in 2009 that a H5N1 biological weapons attack on humanity through “vaccination,” was imminent. He said the H5N1 is even more lethal then the H1N1.

I found an mRNA vaccine patent for cattle using the H5N1 and H1N1 and the deadly Brucella bacteria. This means the cabal has also been producing weaponry in Ukraine, to poison our food supply. The patent is owned by Khazakstanians.

Incidentally, there’s a U.S. bioweapons lab in Khazakstan that weaponized Coronavirus for aerosolized dissemination on civilian populations.

I also found an mRNA vaxxine patent for animals that uses the Brucella melitensis for US and UK cattle.

WEAPONS TESTING

Journalist Dilyana Gaytandzheiva reports that the Pentagon has conducted biological experiments on 4,400 soldiers in Ukraine and 1,000 soldiers in Georgia, and unleashed deadly, antibiotic-resistant bacteria on the local civilian population as well as on allied troops, according to leaked documents.

The documents read that all deaths should be reported to the U.S. Government.The U.S. personnel in these biolabs were given Diplomatic Immunity, although they are not diplomats and they are indemnified from deaths and injuries to the local population.

The Pentagon project in Ukraine and Georgia was code-named GG-21 for “Arthropod-borne and zoonotic infections”.Arthropod-borne means ticks and other insects carrying deadly pathogens to infect Humans. Zoonotic infections are caused by harmful germs, bacteria, parasites, fungi and mold.

Blood samples were being obtained from 1,000 military recruits during their physical exams at a military hospital in Gori, Georgia.

The 13 deadly pathogens that were being tested on the troops are:

Bacillus anthracis

Brucella

Coxiella burnetii

Francisella tularensis

Hantavirus

Rickettsia species

Bartonella species

Borrelia species

Ehlrichia species

Leptospira species

Salmonella typhi

West Nile Virus (WNV)

The Bacillus anthracis (anthrax) bacteria can be disseminated by aerial spraying.I found a patent with a method for removing plasma (DNA) from Bacillus anthracis bacteria using CRISPR/Cas9 system and it’s owned by China. This is how they get Mycoplasmas.

Brucella is another deadly bactera. In the 1950s, the US military developed artillery shells and bombs armed with a bacterium that causes a debilitating flu-like disease in humans. In 2001, the US and DARPA artificially sequenced the Brucella suis genome and began applying it to vaccines.Being infected with Brucellosis is like having the flu times ten, though it’s not life-threatening unless you have some other condition.The US Army likes the Brucella suis pathogen because they’re able to debilitate people without killing them, just like “COVID-19”.

Crimean-Congo hemorrhagic fever (CCHF) has been weaponized using ticks to infect Humans. It has a 40% lethality.Coxiella burnetii and Francisella tularensis are also highly infectious. You need only 10 bacteria to make you sick. The U.S. military was supposed to have destroyed the Francisella tularensis in 1973 because it has up to a 60% lethality.

TBE is tick-borne and causes encephalitis.Bartonella species cause Lyme Disease.Borrelia bacteria hides inside parasitic worms, causing chronic brain diseases.Ehlrichia is a disease from dogs. WNV (West Nile Virus) is carried by mosquitos.

CONCLUSION

Putin just cut off the head of the snake in Ukraine and exposed the whole shit-show. Now let’s make the most of it.