Category: monoclonal antibodies

BREAKING: Anthrax Is The COVID-19 “Vaccine Antigen” And It’s Aerosolized!
Posted on by Ariyana Love

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.

Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero
Posted on by Ariyana Love

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

Snake Venom Key Ingredient In “Covid-19 Vaccine” Patents
Posted on by Ariyana Love

By Dr. Ariyana Love, ND

The world premier documentary Watch The Water aired on Red Voice Media this week. Dr. Bryan Ardis dropped a bombshell during his interview with Stew Peters about one of the greatest conspiracy truths of all time. The intentional poisoning of the world’s population through our municipal water supply using snake venom.

Please see: VenomTech company announces massive library of SNAKE VENOM peptides for pharmaceutical development; “nanocarriers” stabilize snake venom in WATER (PubMed)

SNAKE VENOM PATENTS

Most snake venoms contain proteolytic enzymes. I found Snake venom in ten Covid-19 vaccine patents listed as “venom” and “proteolytic” (enzyme).

Snake venom is being recently touted as an “anti-HIV” drug, since January 2022. There’s six PLA2s from Snake Venoms patents “against HIV”. These synthetically derived snake venoms are marketed under the guise of being “antiviral” and as a preventive treatment for HIV infection.

The study claims snake venom works to “protect against Lentiviruses” through the “destruction of the viral membrane.” However, this is a lie because we know the Lentiviruses are a lab generated, chimeric mRNA bioweapon containing SARS, MERS, HIV 1-3 and SRV-1 (AIDS), as I documented in my article entitled, Transgenic Hydras & Parasites A Biological Weapons System For Rapid HumanCloning.

In actuality, snake venom is being used to destroy the human cell membrane not the “viral membrane”, so that nanoparticles can enter the cell and code your genome.This PubMed study proves that HIV is being encoded into people’s cells to produce a new cell line persistently. So snake venom assists mRNA to clone your cells. The J&J patent also mentions “RNA Replicons” which are forever replicating proteins.

Our Satanic “elites” have programmed the AI to create bioweapons far more complex than humans could ever come up with and the AI came up with 40,000 of the most deadly bioweapons to date.

THE SPIKE PROTEIN

The ACE2 protein acts as an anti-inflammatory, keeping immune cells from inflicting damage on the body’s own cells. The ACE2 receptor helps muscles contract and acts as a messenger between nerves, muscles and cells. It’s crucial in your cell signaling processes.

The ACE2 molecule acts as a gateway, preventing toxins from entering your cells. The mainstream narrative says that SARS-CoV-2 or the “spike protein”, attaches to human cells and blocks the ACE2 receptors. Snake venoms are postsynaptic neurotoxins, meaning they block the Ace2 receptors. So, I think we’ve identified the “spike protein”.

Snake venom latches onto ACE2 proteins and they get knocked out of commission. This destroys the body’s cell signaling function and enables the nanotech weapons system to enter the cells and reach the nucleus, where the mRNA is reverse-transcribed and integrated into the human genome.

Snake venom causes paralysis, the loss of muscle function and respiratory failure. It also causes inflammation, cytokine storms and induces auto-immune illness. Studies say snake venom triggers irreversible intracellular alterations, organ failure and continued cell death.

Heart and lung cells are covered with these ACE2 surface proteins which could explain why there’s so many reports of acute Myocardial injury following “Covid-19 vaccination”. I am receiving a lot of reports from my clients of prolonged stomach pain from these lethal jabs, another causation of snake venom which affects your digestion.

Speaking of digestion, the Food and Agriculture Organization of the US approved the use of snake venom in food last year (2021). According to the FAO/WHO the PLA2 enzyme (snake venom) complies with the General Specifications and Considerations for Enzyme Preparations Used in Food Processing. They’re using a combination of snake venom and a genetically modified Streptomyces violaceoruber bacteria (strain pChi).In other words, it will alter your genome.

Notice the conflict of interest in this safety study that declares the pChi strain is not harmful for consumption. The study does admit that this bacterial strain modifies your genome. I don’t believe that any level of genetic modification of humans is at all safe.

CROTOXIN

60% of snake venom consists of a neurotoxic substance called Crotoxin. It was the first proteinic toxin to be crystallized into protein crystallization.Once crystallized it can be used in structural biology. You can even buy Crotoxin online.

ORGANOIDS

Organoids are being grown a lab to mass produce snake venom. Organoids of snake glands can produce snake venom artificially, without the entire snake.

MONOCLONAL ANTIBODIES

Monoclonal antibodies were funded and developed by DARPA and Bill Gates. All monoclonal antibody patents reveal this is a mRNA “vaccine” that codes your cells with HIV-1. Just like the “Covid-19 vaccines”, monoclonal antibodies never underwent clinical safety trials. They’ve never been approved for use on humans and were passed under the Emergency Use Authorization.

In his interview with Mike Adams, Dr. Bryan Ardis mentioned a study funded by Fauci and the NIH that proved monoclonal antibodies are in fact, unsafe. They specifically target and destroy your T-cells (killer cells) through cytotoxicity. Thermo Fisher’s monoclonal antibodies actually contain snake venom (PLA2)!

Please read: Monoclonal Antibodies Is Experimental Gene Therapy – PatentReview

All monoclonal antibodies contain Hydroxychloroquine or chloroquine in “some embodiments”. This explains why some people report feeling better after using monoclonal antibodies at first and that’s enough to fool doctors but later they become extremely fatigued. The long-term effects are still unknown but they cannot be good. When your immune system is destroyed, your body cannot fight off disease.

NANOBODIES

The Oxford patent mentions “Nanobodies” and says that “antibodies have been replaced with Nanobodies”. The whole purpose of the “Covid-19 vaccines” was to invoke an “antibody response”. Now that lie too is exposed. The nanotechnology is being programmed to kill.

ANTIDOTE

There are breakthrough medicines and supplements that work antidotally against all poisons, including snake venom. In the Dr. Bryan Ardis interview with Dr. Braun, he mentioned the power of redox molecules against snake poison.

A peer-reviewed study from 2018, shows that Melatonin inhibits snake venom and antivenom induced oxidative stress:

“Besides antibodies, molecules like melatonin are reported to underlie the antivenom effect. The study of such was established in Egyptian cobra (Naja haje) venom using a rat model; the vital organs, like kidney, liver and heart, of the rat were protected from the venomous effect.”

Contact me on Telegram for information on where you can obtain the redox molecule supplement that enables your body to remove all poisons and restores all of your body system functions.

Also, follow my Telegram channel here.

Watch my latest interview with Stew Peters at Red Voice Media, here.

Posted on by Ariyana Love

By Dr. Ariyana Love (ND)

Dr. Li-Meng Yan claims to be a “whistleblower” who’s against the CCP. She worked as a virologist in a Hong Kong lab with her husband who is also a virologist.

On February 15th, Dr. Yan supposedly blew the whistle saying she was given inside information that the CCP was planning to disseminate biological weapons at the winter Olympics in Beijing by releasing a “virus” that will induce hemorrhagic fever. She seemed to be setting the stage for us to believe that such an attack would lead to a Marburg outbreak.

While the CCP could easily have unleashed a bioweapon on people attending the winter Olympics, would that actually be able to induce the next staged plandemic, worldwide? I think not.

More than likely this is a ruse and a diversion from the fact that Marburg has already been injected into the world’s population through the Johnson & Johnson “vaccine”. The J&J patent specifically says that it contains Ebola and Marburg, a mRNA bioweapon that induces hemorrhagic fever. In fact, Frontline doctors are already seeing Hemorrhagic Fever showing up in the vaccinated population.

Dr. Yan went on to say that the CCP has an “antidote” calledDarzalex (daratumumab). Darzalex is an experimental drug using monoclonal antibodies. Is it a coincidence that J&J also owns the Darzalex patent and is now conveniently offering the supposed “antidote”? Problem, reaction, solution?

PATENT REVIEW

The Darzalex (daratumumab) patent was filed in 2015 for the treatment of Multiple Myeloma (MM) which is cancer. It was approved in the US by the FDA, for the treatment of patients with multiple myeloma in 2018, despite that a lawsuit was filed against Janssen Biotech Inc. in 2016, for patent infringement.

It is in fact, illegal to use monoclonal antibodies for any other treatment than myeloma, like “covid” symptoms or vaccine injury, for example. Despite that, MM patients have a 4-7 year life expectancy and therefore this is an end of life treatment.

In November 2020, Another monoclonal antibody combination of Casirivimab and Imdevimab made by Regeneron,was approved for use by the FDA for the treatment of Covid-19. It was approved under an Emergency Use Authorization because it’s an entirely experimental drug which uses “laboratory-made proteins”. It has never been tested on Humans and by their own admission, has never been proven safe and effective.

Regeneron warns that you can expect a “worsening of symptoms after treatment that may result in hospitalization”. I suppose that how you know it’s working. Also, the side effects of monoclonal antibodies “may be life-threatening”.

Grant funding for monoclonal antibodies came from the NIH, DAPRA, the Bill and Melinda Gates Foundation, the Musk Foundation, Janssen Pharmaceuticals, Gilead Sciences Inc., Pfizer Inc, and the University of North Carolina Chapel Hill, to name a few. This so called “treatment” is also part of Operation Warp Speed.

In a 2021 video, Bill Gates was promoting monoclonal antibodies as the next singular “treatment” for Covid-19.

Monoclonal antibodies reportedly “block the SARS-COV2 spike protein RBD from binding to the human ACE2 receptor”. However, studies reveal that monoclonal antibodies lessen the likelihood of SAR-CoV-2 resistance by 100 fold.

The Darzalex (daratumubad) patent includes a GenBank Accession Nos. NM_001775 which is a clone Lentiviral vector (nucleic acid sequence) and a NP_001766 is a cDNA (complementary DNA). I have documented previously that the Lentiviral vector contain the SARS, MERS, HIV 1-3, and SRV-1 bioweapons and that “cDNA” is used for cloning and patent eligibility.

The monoclonal antibody patent #10787501 uses “RNA and DNA vectors”, or polynucleotides. The patent also reveals this is a “vaccine“. This is experimental “Gene Therapy” using chimeric mRNA technology.

The patent mentions that “some embodiments” contains chloroquine or hydroxychloroquine while other embodiments contain only the immune suppressing agents. For example, HCDR1R is used in the “treatment” of Lupus which is a “down-regulation” of genes. HCDR2 gene clusters are also used in monoclonal antibodies for DNA binding and gene knockdowns using CRISPR.

Thermo Fischer provides monoclonal antibodies using CRISPR, for gene editing and knockdown. Labome is a key supplier of the “antibodies” used in monoclonal antibodies. Labome’s website admits it’s product is used for Human “cloning“.

The patent also says it contains LCDR2 which has Anthony Fauci’s HIV-1 patented bioweapon vector. It should be noted that the LCDR3 mentioned in the patent is the DNA of a humanized, chimeric mouse/human hybrid species. That’s definitely experimental and unsafe to inject in Humans. Any honest doctor will tell you this.

The patent says “In some embodiments, the coronavirus is selected from the group consisting of SARS-CoV-2, SARS-CoV, and MERS-CoV”. This literally means that monoclonal antibodies contain SARS and MERS. We know that SARS and MERS are bioweapons and that SARS is “aerosolized through the sweat glands”, according to Dr. Hodkinson who gave his testimony to Reiner Fuellmich.

The patent reads: “In any of the various embodiments discussed above or herein, the antibody or antigen-binding binding fragment comprises a VH3-66 or Vk1-33 variable domain sequence.” This PubMed study reveals that “theVH3-53 andVH3-66VHgenesegments encode V regions“.

This PubMed study reveals that “Nucleotide sequences of the cDNAs encoding theV-regionsof H- and L-chains of a human monoclonal antibody specific to HIV-1-gp41“. So, monoclonal antibodies contain HIV-1 which is being encoded into your cells using cDNA. This is cross-species genomics! Also, the HIV-1 bioweapon is patented and owned by Anthony Fauci.

Another PubMed study reveals that the Novel V genes quoted above, do encode cells using mRNA.

Please see: Covid-19 Patent Horrors

Other horrors in the monoclonal antibody patent read: “isolated antibody or antigen-binding fragment thereof that binds a SARS-CoV-2 spike protein comprising the amino acid sequence set forth in SEQ ID NO: 832″…

A company called BacDive provides the “832” gene sequence which is a mycobacterium senuense05-832. It is an “aerobe, mesophilic, rod-shaped human pathogen that was isolated from sputum (mucous)”. This means monoclonal antibodies are lab-generated, bacteria based, chimeric pathogens.

Also mentioned in the monoclonal antibody patent is SEQ ID NO: 202. The “202” sequence patent says this is a “dystrophin gene” which is a nucleic acid being used for “gene silencing“ with “RNA interference”.

There is in fact so many genetic sequences mentioned in the monoclonal antibody patent that it would take days to break it down.

MARKER GENES & mRNA

The second monoclonal antibody patent #US10954289B1 states that marker/reporter genes are implemented using an artificial “Jurkat T cell line” and use Luciferase. This is an immortalized Human cell line that also contains insect DNA (Luciferase). That right there is cross-species genomics, aka cloning.

There are many patents listed within the monoclonal antibody patents. One patent in particular contains chimeric proteins that come from experimental humanized animal hybrid DNA. The patents specify that the chimeric proteins “can enter the cells and deliver the replacement enzyme activity lysosome”. The only way cell penetration is possible is if lipid-nanoparticles are used.

Another patent goes on to say that “recombinant RNA molecules comprising a sequence of a gene-editing molecule mRNA” is being used.

Monoclonal antibodies is a mRNA nanotechnology vaccine.

IMMUNE SYSTEM DESTRUCTION

Monoclonal antibodies target and destroy your body’s T-cells or killer cells while cloning a new hybrid cell line. Your T-cells are a vitally important part of your immune system and without them your body is left without any defense against disease. This will serve as the final nail in the coffin for vaccinated persons, or the “final solution” as Bill Gates calls it. Since the “vaccinated” are loosing 5% of their immune system every week, according to a UK Government study, they can’t afford to loose anymore.

The theory is that monoclonal antibodies suppress your natural immune system, enabling your B-cells to generate an antibody response to chimeric proteins. Do I need to explain how wrong this is? Doctors don’t believe it’s possible to detoxify “vaccinated” persons so instead they use their patients as lab rats for Big Pharma in unethical medical interventions.

Some Naturopathic Doctors like myself are succeeding to detoxify vaccinated persons. You can schedule a consultation with Dr. Ariyana Love (ND) or contact me for more information: metanutrients@protonmail.com.