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

In my latest interview with Stew Peter’s, we discussed how the “Covid-19 vaccine” ingredients listed in the patents, reveal that all these poisonous death shots are deleting genes and genetically modifying Humans for patentability.

GRAPHENE

The Hydrogel patent US8415325B2 is listed in the Moderna patent, here. Hydrogels are also mentioned in a second Moderna patent, here. Hydrogel is listed in the Johnson & Johnson patent, here. Hydrogels are made from Graphene Oxide. Nobody can deny the evidence that Graphene Oxide is in the shots.

GMO HUMANS

All the Covid-19 “vaccine” patents mention gene deletion. All the patents except one, mention “complimentary DNA” (cDNA). cDNA is a chimeric mRNA cocktail that’s being coded into Human cells using artificial genetic sequences in cross-species genomics.

According to the US Supreme Court ruling in 2013, altering Humans with cDNA makes them patent eligible. The court documents show that cDNA is made using modified bacterium and Supreme Court judges ruled it patent eligible. This means that a plant, animal or Human, could be patented and owned if first genetically modified with cDNA.

Mark Steele summarized it perfectly by stating:

In the US, the Supreme Court has ruled that vaccinated people worldwide are products, patented goods, according to US law, no longer human. Through a modified DNA or RNA vaccination, the mRNA vaccination, the person ceases to be human and becomes the OWNER of the holder of the modified GEN vaccination patent, because they have their own genome and are no longer “human” (without natural people), but “trans-human”, so a category that does not exist in Human Rights. The quality of a natural person and all related rights are lost. This applies worldwide and patents are subject to US law.

Since 2013, all people vaccinated with GM-modified mRNAs are legally trans-human and legally identified as trans-human and do not enjoy any human or other rights of a state, and this applies worldwide, because GEN-POINT technology patents are under US jurisdiction and law, where they were registered.”

BACTERIUM, NOT “VIRUSES”

The court document says scientists added 4 plasmids to a bacterium. I already documented in my article entitled, “EPIGENETICS: Vaccines Are deleting Human Genes & Transfecting Cells With Ebola/Marburg,” that E. coli is the base for all these chimeric bioweapons, not viruses.

I found E. coli listed in most of the patents. Mind you, these are genetically enhanced, antibiotic resistant bacterium, made to be them more lethal. They are then transfected into GMO parasites and Hydras. These parasites are more difficult to kill but they can be killed using specific natural protocols.

You can eliminate the entire species with CRISPR-Cas-9 technology or completely remove genetic traits in the Human race. 

FAUCI FUNDED BIOWEAPONS

I previously wrote about the Fauci-funded chimeric bioweapon called the Lentivirus mRNA vector in my article entitled, ” Transgenic Hydras & Parasites A Biological Weapons System For Rapid Human Cloning.” The Lentivirus bioweapon was developed in Wuhan and contains the HIV 1-3, SARS, MERS and the AIDS inducing SRV-1. It can be found in the Moderna, Pfizer, J&J, AstraZeneca and Oxford patents.

The HIV-1 Bioweapon, which contained within the Lentivirus vector, is patented and owned by Anthony Fauci. He is a mass murdering war criminal responsible for this “Vaccine” Holocaust.

PATENT HIGHLIGHTS

The Pfizer patent mentions gene 69-70 deletion and mutation.

Thermo Fischer produced a study revealing that gene deletion mutations is the cause of “vaccine” induced variants. This company is not only profiting from this “Vaccine” Holocaust but Thermo Fischer has a scientific report clearly stating that gene deletion is responsible for the Lambda, Alpha, Beta, Gamma, and Delta variants.

SV-40 vector is a chimeric Bioweapon found in the J&J patent. It’s known to cause rapid cancer growth. The SV-40 vector is provided to J&J by Thermo Fischer. SV-40 contains Human cells, Bovine Growth Hormone (Mad Cow Disease), E. coli, and Herpes. This would explain the Herpes outbreaks after “vaccination”.

The Pfizer patent also mentions gene 144 deletion which causes rapid cancer growth.

I also found a patent for aCombo kit PCRthat mentions gene deletion! So the PCR is not a test at all but implants the mRNA technology without Informed Consent, into your brain.

The Pfizer patent mentions X / Y Chromosome inversions. Inversion of sex genes cause sterility. Since this is a depopulation/extermination and cloning agenda, the transgender Psyop begins to make sense. They want to sterilize our kids and cross-sex hormones will achieve that.

The Moderna patent mentions folding protein and mutations (thus variants) that result in rapid aging and genetic diseases. The patent literally says this is a Loss-of-Function and thus, a gene deleting Bioweapon. 

Moderna’s patents are listed on their website, here

The Moderna patent says it’s using the Bovine Growth Hormone which comes from a cow disease known as Mad Cow Disease. Moderna is cloning Humans with a cow disease that becomes deadly when coded into Human cells. This is an animal disease that does NOT even affect Humans so why is Big Pharma transfecting Human cells with Bovine Growth Hormone when it’s known to induce neurological degeneration, dementia and death?

Here’s a PCR kit patent that “tests” Humans for Mad Cow Disease. Or, does it actually transfect Humans with Mad Cow Disease using the Hydrogels?

The Moderna patents makes “add and delete” references to RNA using cDNA templates. It also has starts codons or Open Reading Frame (ORF. These are no stop codons which means there’s no stop to the gene mutations. The variants will continue on indefinitely, passing through the Human race just as Geert Vanden Bosche said would happen.

Without stop codons, an organism is unable to produce specific proteins. The new polypeptide (protein) chain will just grow and grow until the cell bursts or there are no more available amino acids to add to it.

Moderna’s patent also mentions “induce triple helix formation”. This is the third strand that’s being synthetically added to Human DNA. This study shows more about how scientists are creating the triple helix formation in Humans. Here’s another study revealing the artificial triple helix.

The Moderna “Protocol” says one in two of their shots is a Saline. So that’s a 50-50% Russian Roulette chance with your life and your health. The patent also states that Moderna is “encoding HIV-1“. Once again, that’s Fauci’s bioweapon.

The AstraZeneca patent states an E1, E3, E4 gene deletion. As I documented earlier, these gene deletions induce AIDS, unless you get the Saline. Later the pharmaceutical cartel will be removing all Saline shots.

The Novovax patent mentions gene deletion.

The GlaxoSmithKline patent mentions gene deletion and says it uses H1N1, which is the same chimeric bacteria that was used to kill 500 million people in the 1918 Democide, dubbed the “Spanish Flu”, as this study reveals.

“The trimerization domain (foldon) of T4 phage fibritin, a trimeric beta hairpin propeller, was first used in crystallization studies of the 1918 H1N1.”

Bill Gates said to expect a Smallpox Bioweapon terror attack. Smallpox is made from the N1H1 chimeric bacterium proteins. I documented that previously.

The patents back up what Dr. Pablo Campra’s said in his Stew Peter’s interview, that these death jabs contain Nano-biosensors. I’ll be revealing more about this from the patents very soon!

Conclusion

This is not a weapons system of one country against another. This is a weapons system of the NWO against the entire Human population. The only way this ends is when we stand together as one.

Here’s the World Freedom Alliance Notice of Liability. Any regular citizen can serve anyone with a notice of war crimes, if they are mandating or coercing you to take this poisonous shot which is in violation of your basic Human Rights and Nuremberg Codes. Since this is an international case, the Notice of Liability is served in English, country-wide. 

See original interview with Stew Peters and Dr. Ariyana Love on Rumble, here.

PLEASE SEE: Dr. Ariyana Love: Graphene Covid Kill Shots, Let The Evidence Speak For Itself

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Follow Stew Peters Show, here.

By Dr. Ariyana Love

(Updated Nov. 23, 2021)

Stockholm University just released a scientific horror. The “spike” protein in the Covid-19 “vaccines” are penetrating the cells of the vaccinated, reaching the cell nuclei, and impairing your cell’s ability to repair damaged DNA.

Pharmaceutical “vaccines” are silencing the genes responsible for DNA repair and deleting them forever in humans.

I joined Stew Peter’s Show once again, to break this shocking discovery on Red Voice Media.

Johnson & Johnson uses Adenovirus 26 (Ad26) in its vaxxine. J&J openly admits that their Ad26 vector “codes your cells to produce a spike protein” but they don’t tell you they’re also deleting your genes.

The U.S. patent #20140017278 for Adenovirus 26 and 35 Filovirus, openly states that it codes your cells with the Ebola and Marburg chimeric proteins.

“The filovirus antigenic protein is usually a glycoprotein from an Ebola virus or a Marburg virus.”

The J&J Adenovirus 26 vector deletes your E1 gene. The patent also states that it deletes the E1 gene in Humans. This is known as the X Chromosome. The E1 gene is required for accurate and instant repair of damaged DNA. Deletion of this gene is lethal.

E1 gene deletion causes embryonic lethality which means permanent sterility for men and women. It causes Lactic Acidosis in children which is the lack of oxygen in the blood. E1 gene deletion causes rapid cancer growth, Thrombosis, and the coagulation of the blood which leads to clotting. Blood clotting is the main reason people are dying from the Covid vaxxines.

E1 gene deletion causes Mitochondrial DNA-Associated Syndrome which is a process of glucose metabolism deficiency that exists in various diseases such as Alzheimer’s, epilepsy, diabetes-associated cognitive decline, and severe neurological disorders such as Leigh’s Syndrome. There’s a progressive loss of mental cognition and typically results in death within two or three years, usually due to respiratory failure.

Without your E1 gene, your cells will literally self-suicide.

U.S. patent #10695417 is the Human Adenovirus 5 vector that contains E1 and E2B gene deletions. The Adenovirus 5 vector is used in Sinovax and it encodes the cells with Ebola Glycoprotein. Glycoprotein-41 andglycoprotein-120 are HIV viral coat Proteins and Glycoprotein plays a key role in reproduction.

Sinovac is used in China, Chile, Brazil, Turkey, and the Philippines.

The Adenovirus 5 vector was developed through Gain-of-Function research.

Knocking out the E2B gene caused sterilization in male mice.

You can order the chimeric messenger RNA of the Lentivirus and the Adenovirus 5 vectors or Baculoviridae online from Thermo Fischer, for recombinant cross-species genomics (cloning).

Thermo Fischer explains how the Adenovirus 5 targets and enters the bronchial epithelial cells (lungs) and deletes the E3 and E4 genes, intentionally inducing Sjögren’ssyndrome which is long-term autoimmunity (AIDS).

Loss of your E4 gene deletes your cognitive function. Deletion of your E3 gene degenerates your brain, causes dementia, gradual loss of memory, judgment, and the overall ability to function.

Here’s a study describing how you knockout the E3 gene.

The knockout of these genes affects the moisture-producing glands of your body. It’s not the “spike protein” that’s causing the blood of the vaxxed to coagulate, it’s the gene silencing (deletion). Without moisture, your blood coagulates and clots. The deletion of these genes also causes gastrointestinal disorders.

Adenovirus 5 also alters the cell signaling pathways and leads to Lymphoma due to destruction to the immune system. This causes cancers to grow and the blood to coagulate.

This is proof positive they’re creating the next “pandemic” with lethal injections that will gradually induce AIDS in the inoculated masses through gene deletion.

The pharmaceutical cartel has not only injected Ebola and Marburg into people but they’re also transfecting people’s cells with these catastrophic chimeric pathogens. The vaxxed will battle chronic infections and lifelong disabilities while the cells of the vaxxed continuously replicate with the synthetic genetic sequences of Ebola and Marburg until it kills them unless they detoxify continuously.

The immune system of the vaxxed is depreciating 5% each week according to a recent UK Government study. Everyone who vaxxed age 30 and above, will have no immunity left by Christmas. But that’s not all.

As the cells of the vaxxed replicate Ebola and Marburg “spike proteins” and their cells decay and die, they will shed the chimeric disease throughout the population via transmission. Therefore it’s crucial for the unvaxxed to continuously detoxify as well.

According to a UK government declaration from the NIH, we are presently in a Phase III clinical trial on Humans using the Adenovirus 5 vector to “fight Covid-19” which began on January 22, 2021.

“This is a global phase III clinical trial to evaluate efficacy, safety, immuogenicity of Ad5-nCoV manufactured by Cansino and Beijing Institute of Biotechnology in health adults aged 18 years old and above.”

So the UK Government is partners with the Chinese Communist Party (CCP) to exterminate Humans.

The World Health Organization (WHO) also published on their website that we are in an Ebola Vaccine Stage III Clinical Trial.

WHO published that we are in an Ebola Vaccine Stage III Clinical Trial

Later the WHO scrubbed it from their website.

Viruses are still an unproven theory. Given the advances in scientific lab equipment and considering that we’re able to observe nanotechnology under microscopy and spectroscopy, would somebody please explain to me why we still can’t identify a virus? Could Germ Theory be the big pharmacopeia lie in modern medicine and Terrain Theory be the more relevant truth?

Governments enhanced the airborne transmissibility in mammals (Humans) of highly virulent avian influenza strains. The history of making pathogens transmissible goes back at least to the synthesis of viable influenza H1N1 from 1918. Incidentally, the 2009 swine flu Pandemic was also induced by inoculation using the H1N1 vaxxine. So this is nothing new under the sun.

Sinister shadow governments have been weaponizing nature, producing diseases through vaxxine injection and genetically manipulating Humans for at least the past 100 years. But where did they get this technology to do it?

The U.S. National Library of Medicine revealed something rather interesting. The USSR’s ‘invisible anthrax’ is a Gain-of-Function bioweapon created by introducing an alien gene into Bacillus anthracis (bacteria). That’s how they made Anthrax. They used an alien gene and genetically altered bacterial immunological properties to produce a deadly pathogen to Humans. Where did they get an alien gene from? A UFO crash perhaps? Negotiations with other beings? Your guess is as good as mine.

The U.S. Government has been testing this germ warfare technology on its own military troops since the 1950s, using Adenovirus 4, Ad5, and Ad7 vectors with HIV encoding Envelope (clade C.1086). The Ad7 vector delivered in enteric capsules has been used to “vaccinate” U.S. military personnel “against respiratory and gastrointestinal illness”, since the 1970s.

Monkeypox is also made from the same bacterial pathogens as Ebola and Marburg. Ebola and Marburg can kill nine out of ten people it infects. Although this is not really an infection, it’s transfection (human cloning).

Ebola and Marburg cause hemorrhagic fevers (VHF). They simultaneously affect multiple organ systems in the body and may be accompanied by hemorrhage, or bleeding. These pathogens cause high fever, chills, muscle aches, and vomiting. The patients worsen rapidly until they bleed from every orifice in their body, including needle puncture wounds. They usually die within 1-3 days.

Bill and Melinda Gates say on their Gavi website to expect the next pandemic to be a Marburg outbreak. These two psychics or psychos also claim that Ebola and Marburg are carried by African Green Monkeys.

The lying CDC claims that people can get “Ebola Virus disease” through direct contact with an infected animal (bat or nonhuman primate). They’re taking the absolute piss out of us! Never in the history of medicine has an animal disease infected Humans! The only possible way to make a Human diseased with an animal disease is through cross-species genomics using Adenvirus or mRNA and Nanotechnology.

Polio vaccines used in the late 1950s and early 1960s were intentionally contaminated with a bacterial pathogen called the “Simian Virus” 40 (SV40) present in monkey kidney cells. The Simian Virus is used for infecting Humans. It was “accidentally administered to Humans” through Polio vaxxines.

The “Vaccinia virus” is similar to the “smallpox virus” but it’s not naturally occurring after all. Scientific Direct reported that “vaccinee-to-cattle and cattle-to-human Transmissions occurred on Farms”, proving the transmission of pathogens between animal to human species is being done by genetic engineering and administered through vaxxines.

Knocking out the E1 and E3 genes is necessary when transfecting cross-species in order to make the pathogen replicate. The Vaccinia pathogen has been used on a wide scale to produce many different kinds of chimeric proteins, including HIV-1 and it encodes approximately 250 genes.

Ebola and Marburg are GAIN-and-Loss-of-Function bioweapons and both are created using the “Green Monkey disease“, a chimeric pathogen that you can purchase online!

Adenovirus’ are from human/monkey clone origin and are used with chimeric Lentiviruses, as well as the Filoviruses. Of course, none of these are actual viruses! All the Adenoviruses and messenger RNA (mRNA) are chimeric weapons used to code your cells to reproduce deadly proteins used to both silence genes and program artificial genetic sequences. They are inducing diseases and making up disease names and syndromes to hide the fact that it’s coming from vaxxines!

Ebola, Marburg, and Monkeypox are Gain-of-Function bioweapons created using the “Green Monkey disease”. It’s an Adenovirus made from E. coli bacteria from the decaying flesh of a human/monkey hybrid’s kidney tissue culture. Adenovirus vectors transfect Humans with monkey DNA, Ebola, and HIV. Adenovirus vectors are transfecting humans with monkey DNA and Human DNA from a Chimpanzee/Human clone to be exact.

There are 49 immunologically distinct types of adenovirus that can cause infection for long-term gene expression. They’re made with Sialic acid which is a group of derivatives of Neuraminic Acid found in animal tissues. Sialic acid is the primary entry receptor used in Adenovirus.

Sialic Acid is an animal DNA from “Species D” Adenovirus which is used in both Adenovirus 5 and Adenovirus 26 (Sinovac and J&J) to transfect Ebola and HIV into Human cells using Sialic acid-bearing glycans (animal DNA) as a primary cell entry receptor. Adenovirus 5 is of “Chimpanzee origin”. There’s that Green Monkey clone again!

Sialic acid proliferates tumor growth and metastases. N-acetylneuraminic acid (Neu5Ac) is made from E. coli bacteria. See the study’s here and here.

Polio vaxxines used in the late 1950s and early 1960s were “contaminated with a virus” or rather a bacterial pathogen called the Simian Virus 40 (SV40) which is present in monkey kidney cells used to grow the vaxxine.

The Pharma death cult is inducing diseases with their vaxxine racket and making up names and syndromes that they can then profit from by “treating” later when people become diseased. What would life be like without the Pharma cartel disabling our children and killing healthy people in the name of science and medicine?

There are no viruses involved in the making of any of the mRNA or Adenovirus vaxxines, only GAIN-and Loss-of-Function chimeric pathogens made from bacteria and other plasmids which Pharma keeps naming “viruses”.

There’s no “spike” from a virus particle being used in any of these vaxxine induced diseases. We should change our language from “spike protein” which is a half-truth with a half-lie and replace it with “chimeric protein” to be medically accurate because that’s what we’re dealing with.

E. coli bacteria are used as the base for all these chimeric diseases because bacteria DNA replicates. They’re also using other plasmids and mixing fungus, yeasts, and “several mammal-based systems” (Human/Chimpanzee clone), then genetically enhancing them to increase lethality.

They’re also using baculovirus-mediated insect cell expression. This means the Pharma cult is transfecting human cells with insect DNA. This could explain the strange mutations and Morgellons.

Marburg is simply Ebola with Ricin added to make it more lethal. Both cause hemorrhagic fevers (VHF) and attack multiple organ systems in the body, accompanied by bleeding.

The Pharma death cartel and the Eugenicists already have a PCR kit for “testing” for Marburg disease and a vaxxine to immunize against, called RiVax. The main component of RiVax is “a genetically altered version of a Ricin Toxin.” Ricin is more toxic than Graphene Oxide, by the way.

I think it’s high time people stop trusting our governments, stop relying on government and take our children out of public schools, as Dr. Zev Zelenko said to Alex Jones on Info Wars. Don’t sacrifice your kids to Satan.

My detox protocol works for the vaxxed and the unvaxxed to kill the Micro-plasmids (parasites, transgenic Hydra’s and bacteria) and reverse the coagulation cascade which leads to blood clots.

PLEASE SEE: DR. LOVE’S DETOX PROTOCOL

For consultations or if you have questions please don’t hesitate to reach out to me: metanutrients@mailfence.com

By Dr. Ariyana Love

“That Thing” was discovered in the Covid Vaxx under microscopy by Dr. Carrie Madej and released on Stew Peter’s Show, on September 29th. It turned out to be a transgenic Hydra Vulgaris.

Because Pharma savages purposefully hide their injurious vaxxine ingredients under a trade secret, I knew the only way to get to the bottom of the mystery of why Hydras and parasites are in the Covid Vaxx, is to read through the peer-reviewed literature. A tedious job that even evades experts.

I appeared on the Stew Peter’s Show on October 27, to break my findings.

DOCTOR: HYDRAS AND PARASITES IN VAXX, TRANSFECTING HUMANS INTO NEW SPECIES

https://www.bitchute.com/video/GaBPbjvQGqjn/

Transgenic Hydra lines were developed for GAIN-and Loss-of-Function use in humans at the Wuhan Institute in China and funded by Anthony Fauci, the NIH, and partly by DARPA. Karen Kingston revealed on Stew Peter’s Show that the patents holders are Israeli Zionists.

Hydras and parasites are being first transfected with chimeric pathogens using Plasmid DNA (E. coli bacteria and fungus) to produce a new genetically modified line of Hydras. They are coded with the synthetic genetic sequences of the Lentivirus and Luciferase. These are the infamous “spike proteins” that are being coded into human cells using the Covid-19 “vaccination” program.

Lentivirus is a combination of SARS, MERS, HIV 1-3, and SRV-1 (AIDS). Luciferase is a luminescent Green Flourescent Protein reporter system that allows for the 24/7 tracking of hybrid humans (the vaxxed) through an external computer interface. These are GAIN-and-Loss-of-Function bioweapons.

Transgenic Hydra lines work as vectors, carrying the messenger RNA (mRNA) of the Lentivirus and Luciferase. The GMO Hydras polyps and parasite eggs are carried on the lipid coating of programmable nanoparticles which are delivered on Graphene Oxide sheets.

The coding of human cells with chimeric “spike proteins” through Reverse Genetics, is done by electroporation using programmable Gold Nanobots and CRISPR-Cas9. This technology is all part of an operating system that’s being shot into the veins of our children for the purpose of transfecting them with the most deadly pathogens ever created by governments.

Transgenic Hydra and parasites are assimilated into the human host through Homoplastic transplantation. Once human cells are coded with the artificial reporter genes, the cell signaling of the human alters permanently and synthesizes with the transgenic Hydras cell signaling, called Cantenin Signaling. The entire process of cloning ultimately constructs a new neural network and an artificial brain in humans, as well as a third strand to the DNA.

BLAST technology is being used to create new DNA sequences for cross-species genomics, and yes, this is cloning. The Covid Vaxx inserts an operating system enabling a computer interface that stores your internal data on an external database, for totalitarian control of transgenic humans (the vaxxed) using the Internet.

The operating system is gene silencing and knocking out the genetic sequences your patent holders don’t want you to have, while coding your cells with new, artificial genetic sequences through external interfaces. Essentially, they’re playing god’s. Your patent holders will be able to upregulate and downregulate your genetic sequences through external controls. This is called the “Hybrid Genome Assembly”.

The intended result of this genetic experiment is a mass die-off and rapid cloning of the human race to create an artificial hybridized species. Most people will become sterilized after Covid-19 inoculation and their lineage terminated, many will die and be exterminated because the human body cannot withstand this toxic experiment.

A small percentage of genetically cloned humans will be able to procreate but I strongly advise the vaxxed DO NOT PRODUCE OFFSPRING because they will not contain our God-given human genetic codes! Your offspring will not be human. If you want to have children for God’s sake, do not take the Mark Of The Beast. The operating system targets embryonic cells also cloning your offspring and thus hybridizing future generations. Cloned genetic mutations are always unpredictable so there is a great risk to your hybrid children.

A breaking news report from Mike Adams, The Health Ranger of Natural News, revealed a new scientific discovery that is indeed a “true horror”. Catch the Brighteon podcast here.

Stunning new research published in Viruses, part of the SARS-CoV-2 Host Cell Interactions edition of MDPI (Open Access Journals) reveals that vaccine spike proteins enter cell nuclei and wreak havoc on cells’ DNA repair mechanism, suppressing DNA repair by as much as 90%.”

Make no mistake about it humanity is facing a totalitarian biological attack using a very advanced weapons system that contains programmable nanobots and GMO’d microscopic organisms. Everything I’m reporting here is open-source, viewable online, and linked into my article on Red Voice Media entitled, What’s In the Vaxx? Transgenic Hydra And Parasite Implants Used As Rapid Human Cloning weapon system.

Dr. Christiane Northrop appeared on Gene Decode with Nicholas Veniamin to discuss detox protocols. Nicholas revealed that organic/synthetic insect DNA is also being used in the vaxx and this is what’s causing Morgellons.

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