COVID-19 Vaccine Antigen Is Anthrax

"When there is a lack of honor in government, the morals of the whole people are poisoned" - Herbert Hoover

UPDATED January 10th 2025

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.

SEE INTERVIEW: NIH Using DEAD CORPSES To Make "Virus"; Gain Of Function Weaponized Dead Corpses To Create Deadly Skin Eating Viruses

During my interview with Stew Peters in 2023, I revealed that 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”, which contains deadly Anthrax.

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 Israel’s IDF conducted animal trials for the Anthrax “vaccine” and human trials reporting that it was “safe and effective”, despite violating the Helsinki Convention.

Meanwhile, Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014, while 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 demonstrates severe adverse reactions.

The Israeli state, NIH and China turned their more lethal Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.”

A natural pathogen can be used to evoke an immune response in Vaccinology, but a Gain-And-Loss-Of-Function, lab enhanced bioweapon cannot be called an “antigen”. Nations have been intentionally tricked into poisoning themselves with biowarfare, under the guise of safety.

In March 2022, I broke the news on Stew Peters Show, that the Russian military discovered Covid-19 bioweaponry is being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more.

Anthrax causes hemorrhaging and so does Ebola and Marburg. This would explain all the strange bleeding Covid-19 “vaccinated” individuals are experinecing. It’s due to Anthrax poisoning.

SEE INTERVIEWS: Putin's Secret War: Ukrainian Bioweapon Labs Exposed

Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both made from Anthrax but have different potentiates and blends of poisons.

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Please see: EPIGENETICS: Vaccines Are Deleting Human Genes & Transfecting Cells With Ebola/Marburg

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H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs. The Anthrax “antigen” is now used in most “vaccines”, worldwide.

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 “antigen” from replicating inside the human body after inoculation, due to it being antibiotic resistant.

This is an extremely important point to emphasize. The Rockefeller medical industrial complex is rigged to fail. The allopathic hospital system is not equipped to treat the “vaccine” injuries. In addition, nanotechnology slips under the radar of their diagnostic equipment. Antibiotics will not destroy the genetically modified bacterium (Anthrax) that has been introduced by inoculations and is circulating throughout the population worldwide. Antibiotics will only deplete your vital immune system and make you more susceptible to infections, enabling the Anthrax-based bioweapon to continue replication throughout your body. In my experience, only natural treatments are effective at detoxing Anthrax and other toxic GMO bacteria.

The B. anthracis bacteria was also genetically modified to survive in insect hosts, so as not to sporulate before injection into the human host by one of Bill Gates’ genetically attenuated mosquitos. This is all 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 has emphasized that a bioterrorist attack would most likely be Anthrax.

SEE INTERVIEW: Dr. Ariyana Love - Bioweapons, Ethnic Cleansing of the Western World & Doherty Institute

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

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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. “Vaccinating” against a bioweapon using that same bioweapon, now that is indeed novel.

There exist two patents for an “Aerosolized Anthrax Vaccine” for humans. I would like to emphasize that they are both aerosolized.

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”). When a gene is deleted from an organism's genome, the corresponding protein encoded by that gene is effectively "inactivated" because the genetic instructions to produce it are missing, resulting in no functional protein being made. It’s otherwise known as gene knockouts. These knockouts are done using CRISPR.

The molecular basis of Anthrax “vaccines” includes "spores and DNA plasmids” which 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, for targeted “drug delivery”. Pharmaceutical drugs of the past were ingested, injected or infused, but these days Pharma and governments are altering the human genome and encoding the genome of target cells to replicate and reproduce an artificial genetic sequence, any pharmaceutical drug of choice, even when that drug is an unlawful bioweapon like Anthrax.

So the question remains. Are “vaccines” really for medical drug delivery or have they been updated to rapidly take out your immune system and induce an accelerating death?

ALHYDROGEL

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

According to patents, the main ingredient in aluminum compounds used for “therapeutics” in “vaccines” are aluminum and a protein based 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 a biosensing technology for both military and public health. This is lactate sensors for continuous physiological monitoring. The idea was to create a “chemical substance that’s identical to what’s underneath the skin” and goes on to say that this substance “incorporates itself into the tissue” and the biosensing can “continue on for years”.

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 layperson terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. CD4-T cells are also just called T-cells and comprise an essential part of our immune system. T-cells attack and destroy foreign invaders and prevent them from penetrating our cell membrane. By destroying our T-cells, this enables Pharma’s operating system to take root in the body.

A study entitled, Alum-functionalized graphene oxide nanocomplexes for effective anticancer vaccination, reveals that Alhydrogel is a graphene oxide based aluminum oxyhydroxide, targeting T-cells.

The study shows that Alhydrogel is a graphene oxide nanoparticle-based technology. This explains why Alhydrogel replicates so rapidly throughout the human body after subcutaneous injection, forming a biofilm from head to toe. It’s also taken up into the human genome within about an hour, as Dr. Peter McCullough reports.

Alhydrogel is also infused with 750 μg of aluminum, making it paramagnetic and thus externally controllable with EMF frequency devices. Graphene oxide 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 is literally wiring a new neural network within the human body.

Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant on the market. There are 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?

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 (Alhydrogel) were introduced.

Another peer-reviewed article continues by saying that the “influenza vaccine” was the first to use Alhydrogel.

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

“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. 

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.

GRAPHENE OXIDE

After La Quinta Columna’s groundbreaking discovery in June 2021, that Graphene Oxide Nanoparticles (GON) are in the Covid-19 “vaccine” vials, Karen Kingston followed-up with a reveal on the Stew Peters Show, where she demonstrated that GON are hidden within Covid-19 “vaccines” under a trade secrete.

I also published an article on Graphene Oxide being the vector for the Covid-19 democide in July 2021.

This was hotly debated by medical teams and other experts, many of whom denied the possibility of GON being in Covid-19 “vaccines” despite the quantitative evidence from 22 independent research teams proving otherwise, with La Quinta Columna and Dr. Pablo Campra from the University of Almeria the first to expose it, and the European Parliament backed the evidence.

However, when a bombshell was dropped in September 2024, after the U.S. Federal Court ordered the FDA to publish the controversial Pfizer documents which proved, without a shadow of a doubt, that Graphene Oxide is in fact being used in Covid-19 “vaccines”, the detracters fell silent.

Scientific studies reveal that DARPA’s Alhydrogel is carried in the lipid coating of nanoparticles. Other studies show that it’s aerosolized after subcutaneous injection. Also see here, and here.

GMO PARASITES

The “Aerosolized Anthrax Vaccines”, not surprisingly, 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.

In a series of two videos, myself and Dr. Robert Young gave an in-depth presentation on the genetically modified parasites (SEQ ID NO: 1) being used in Covid-19 “vaccines” back in 2022, exposing Pharma’s use of exotic parasites for gene delivery. Dr. Young brought lab images and I provided receipts. Karen Kingston backed our research, calling these “AI parasites” in an interview with Stew Peters.

The NIH published their development of GMO protozoan parasites used for “genome editing” in January 2021.

The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug and bioweapon that is Anthrax. 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 Alhydrogel, which is an Anthrax spike protein. A person starts producing the toxic spike protein and shedding Anthrax into the air, carried by GON, exposing others to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized in “vaccinations”.

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

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ANTHRAX SYMPTOMS

Anthrax can be 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 via the Covid-19 jabs, contaminated PCR swabs and Bill Gates aerosolized Smart Dust.

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, making it 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 these pharmaceutical drugs are mRNA gene therapy and another weapon system.

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

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Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” 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, such as severe heart issues. Could the Anthrax-based Alhydrogel be a contributing factor to the rise in Myocarditis and Pericarditis after Covid-19 inoculations?

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. So Anthrax is a contributing factor to blood coagulation from Covid-19 jabs.

Anthrax also induces hemorrhaging. This would explain all the excessive bleeding from every oriface the “vaccinated” 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 evident 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.

A study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms the phenomenon is Mycoplasma Pneumonia.

All naturally occurring bacteria 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 coagulation and proinflammatory cytokine signaling and other studies show histological lesions in the spleen.

Anthrax has already been tested on the human public as well. 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 (investigations) in the history of law enforcement”, according to the FBI. 

Heroine users in Europe have been tested with Injection Anthrax. 

A 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.

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.”

CONCLUSION

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. Essentially, we’re dealing with more than just Anthrax. Alhydrogel is a toxic bacteria soup that must be counteracted with a protocol of very potent and natural antibacterials.

No matter what laws and/or mandates governments pass to enforce you to participate in a genetic experiment without your Informed Consent, please know that is in direct violation of the Nuremberg Codes and international law. It’s very important to understand this. Nobody has the right to medically experiment on others without their knowing about it, including governments.

In addition, international law supersedes all government laws, so when a government tries to coerce or force you into an illegal medical experiment, they are in direct violation of international humanitarian laws and can be held accountable. They must be served with a Notice of Liability for their illegal conduct. World Freedom Alliance offers free Notice of Liability downloadable packets.

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 the “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 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 suddenly hot and severely flushed immediately upon exposure, and you may break out in big, red splotches on your skin, followed by a completely red eye or eyes, 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, the NIH admits you need an effective natural medicine detox protocol.

I’ve been successfully detoxing people from Covid-19 poisoning for the last 5 years (since 2020). Once I discovered Anthrax Alhydrogel, I began treating my clients who presenting with Anthrax poisoning, using a proprietary Microbiome Protocol that includes a special preparation for very strong antibacterial tea, or what I like to call a medicine soup. As a result, my clients are experiencing rapid detox results.

If you would like to schedule a consultation with me, please see consultation options and my client retainer package services, through my online booking system.

You can follow me on Telegram @drloveariyana and on X @drloveariyana.

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UPDATED June 8th 2024

In an interview on InfoWars, Karen Kingston revealed that “DARPA hydrogel contains Graphene Oxide Nanoparticles”.