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.

“The Masters of Evil Terrorize Global Citizens by Spraying Down Cities and Towns with Aerosolized Biosynthetic Ai Nanoweapons called Spike Proteins.” – Karen Kingston

by Dr. Ariyana Love

Recently I teamed up with the legendary Dr. Robert O. Young for a mega bombshell reveal about the mRNA vectors in COVID-19 vaccines.

Dr. Young is a senior scientific researcher who’s been analyzing body fluids with specialized lab equipment for over 40 years. I am a second generation Naturopathic Doctor and a 13-year veteran journalist and researcher. Like me, Dr. Young is a targeted individual.

After providing a proven cure for cancer in 1996, Dr. Young fell under attack by the Luciferian cabal who’s been hell bent on smearing his good name ever since. I have been targeted by the Izraeli state since 2017 who’ve been hell bent on smearing my good name with accusations of “racism”.

Dr. Young and I share the same views on medicine and how the body system works to heal itself from, toxic poisoning and injury. So we decided to discuss the root cause of disease and address the increase of parasitic infestation Dr. Young is seeing in clients, from all over the world. Dr. Young gives chilling evidence of unprecedented parasitic infestations in humans, of which he’s not seen in his entire career. He told that parasites are now showing up in 90% of the blood of VAXXed and non-VAXXed individuals alike.

PLEASE WATCH: Part 1 on the Root Cause Of Disease and GMO parasites:

Dr. Robert Young and Dr. Ariyana Love: “The root cause of disease & GMO parasites”

We followed up with a second broadcast for a patent review on the messenger RNA vectors being genetically modified parasites. These GMO parasites are mRNA vectors of deadly synthetic biology that’s being used by Moderna, Pfizer, Novavax, Janssen (J&J), Oxford, and more, to transform the human genome and turn humans into synthetic biology. That’s right, pharmaceutical companies are now using deadly parasites as mRNA vectors for delivering artificial genetic sequences into the human genome through the COVID “vaccination”.

PLEASE WATCH: MEGA BOMBS! Deadly GMO Parasites are the mRNA Vectors: Patent Review with Dr. Young and Dr. Love

Since our great reveal on September 28th, Pfizer whistleblower and patent expert Karen Kingston heroically delivered more bombshell information on Stew Peters Show. She eloquently tied together all aspects of this biological attack against humanity, disclosing that the GMO parasites as mRNA vectors were created with the intention of hooking humans up to AI.

Incidentally, Karen Kingston is also a targeted individual.

PART 1: PROOF COVID Is A PARASITE; Biotech Analyst Has PROOF COVID & Vaxx Are Biosynthetic Parasites

Karen Kingston on Stew Peters Show – Part 1

PART 2: PROOF COVID Is A Nano-weapon PARASITE; Biotech Analyst Has PROOF COVID & Vaxx Are Biosynthetic Parasites

Please also review Karen Kingston’s accompanying article to see additional shocking evidence of this biological assault: Part 1: Dismantling the the Deceptions of the COVID-19 Story.

SEQ ID NO: 1 and SEQ ID NO: 2

There are hundreds of SEQ ID NO’s contained within the COVID serums. We are going to examine just the first two.

SEQ ID NO: 1 is patented and owned by the Pirbright Institute which is owned by Bill & Melinda Gates. It contains polypeptides or amino acid sequences. These are artificial proteins containing synthetic genetic sequences, in other words it’s synthetic biology. These artificial genetic sequences are messenger RNA.

SEQ ID No: 1 is “VACCINE” Patent #20130216569.

The SEQ ID NO: 1 Patent #20130216569 explicitly states that it contains the following deadly protozoan parasite pathogens; Toxoplasma Gondii, Eimeria, Plasmodium, and Theileria.

SEQ ID NO: 2 is owned by Boston Biomedical Research Institute and receives significant funding from the NIH, thus Anthony Fauci. SEQ ID NO: 2 is also synthetic mRNA proteins designed to target and prevent “embryo implantation” in mammals. FYI, humans are classified as mammals.

Embryo implantation is the moment when the fertilized egg is detached from its sheath (zona pellucida), adhered to the endometrium and anchored to it to begin its intrauterine development. Embryo implantation occurs between 5 and 6 days after fertilization. Essentially, SEQ ID NO: 1 aborts embryonic development within the first few days of conception.

SEQ ID NO: 1 can be found within the Pfizer, Moderna, Novavax, Janssen (J&J), Oxford and more, in the COVID jab patents. SEQ ID NO: 2 is found in Moderna, Pfizer and Novavax and more.

PFIZER

Pfizer Coronavirus Vaccine Patent #WO2021213945A1 contains both SEQ ID NO: 1 and SEQ ID NO: 2, deadly protozoan parasites and birth control without Informed Consent.

Pfizer vaxx patent

MODERNA

Moderna Sars-cov-2 mRNA Domain Vaccines Patent #WO2021159040A2 contains SEQ ID NO: 2 birth control without Informed Consent.

Moderna vaxx patent #1

Moderna Delivery and Formulation of Engineered Nuclei Acids Vaccine Patent #US10898574B2 contains SEQ ID NO: 1, with deadly protozoan parasites without Informed Consent.

Moderna vaxx patent #2

NOVAVAX

Novavax Coronavirus Vaccine Formulations Patent #US20210228709A1 contains both SEQ ID NO: 1 and SEQ ID NO: 2 thus it contains both birth control and deadly protozoan parasites without Informed Consent.

Novavax vaxx patent
Novavax vaxx patent

JANSSEN (J&J)

Janssen (J&J) Compositions and Methods for Preventing and Treating Coronavirus Infection-SARS-Cov-2 Vaccines Patent #WO2021155323A1 contains SEQ ID NO: 1 with deadly protozoan parasites.

Janssen (J&J) patent

OXFORD

Oxford Compositions and Methods For Inducing An Immune Response Vaccine Patent #WO2021181100A1 contains SEQ ID NO: 1 with deadly protozoan parasites.

Oxford vaxx patent

PARASITES AS mRNA VECTORS

This BMC study verify’s that deadly parasites were indeed developed as messenger RNA carriers by the World Health Organization, in 2018. The most deadly of the 5 Malaria parasites, Plasmodium falciparum, the Toxoplasma gondii, the Trypanosoma cruzi and the Plasmodium spp. in particular, are all mentioned as mRNA vector exports for vaccines in mammal (human) cells.

This illustration shows the GMO parasite mRNA vectors in brown squiggly lines with a round head. You can see there are things attached to the parasites and a coil at the parasites tail to represent the genetic sequence. This graph outlines how the parasites enter the cell membrane through ruptured holes and make their way to the cell nucleus where it delivers the mRNA and genetic changes are made to the cellular DNA.

mRNA parasites – BMC

According to the NIH website:

“Chagas’ disease is caused by the protozoan parasite Trypanosoma cruzi and causes potentially life-threatening disease of the heart and gastrointestinal tract.”

Is the COVID inoculation inducing a parasitic attack on the heart and other vital organs like the liver, placenta and women’s reproduction? Is the “Myocarditis” diagnosis actually CHAGAS?

Below is a recent lab photo taken by Dr. Robert Young which demonstrates a parasitic infestation in the human cell of one of his clients.

Dr. Robert Young image

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For information on how you can detox and fortify your immune system against this biological attack, you can schedule a consultation with Dr. Love, here.

Please consider donating to Dr. Love’s research, here.

By Dr. Ariyana Love, N.D.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

PATENT

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

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

The CDC is also involved in this VAR2CSA bioweapons development.

STERILIZATION OF THE NATIONS

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

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

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

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

RECOMBINANT VIRAL VECTOR “VACCINES”

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

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

CHAD63 MVA ME-TRAP

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

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

PCR

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

CSVAC

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

FUTURE DIRECTIONS

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

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

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

UPDATE: 6/6/2022

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

By Dr. Ariyana Love, 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.

By Dr. Ariyana Love, N.D.

Intro:

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

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

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

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

GENETIC WARFARE

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

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

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

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

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

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

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

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

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

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

BACKGROUND

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

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

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

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

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

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

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

H5N1 & H1N1

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

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

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

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

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

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

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

WEAPONS TESTING

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

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

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

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

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

Bacillus anthracis

Brucella

Coxiella burnetii

Francisella tularensis

Hantavirus

Rickettsia species

Bartonella species

Borrelia species

Ehlrichia species

Leptospira species

Salmonella typhi

West Nile Virus (WNV)

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

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

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

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

CONCLUSION

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

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.

By Dr. Ariyana Love, ND

Dark Field Microscopy image of Graphene Hydroxide nano-razorblades

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

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

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

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

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

MICROSPHERES & MICROBUBBLES

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

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

Microbubbles and Microspheres (bottom right)

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

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

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

Crystalline scaffolding from the #DeathJab

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

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

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

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

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

Moderna patent US10703789B2 delayed drug release

QUANTOM DOTS & MICROBEADS

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

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

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

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

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

Dr. Ariyana Love on Stew Peters Show, Dec. 9, 2021

Microbead patent US20110017493A1, verifies that Microbeads “carbon based” (made from Graphene) and Microbead patent ES2784361T3/en specifies that it’s used to create molecular barcodes in Humans.

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

THE ISRAELI STATE

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

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

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

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

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

BIOCHIP & HYDROGEL

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

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

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

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

PROTOCOL

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

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

Follow Red Voice Media, here.

Follow Stew Peters Show, here.

(Originally published on )

NOTE: Sometimes the patents read ambiguously and in code language. They refer to the “Spike Protein” which is synonymous with the “Glycoprotein S”. Other times the descriptions could be referring to RNA and DNA changes, like coding new genetic sequences using “cDNA”. They sometimes read with words “in some embodiment’s” which likely means in some vials.

TABLE OF CONTENTS:

Moderna

Pfizer

Janssen (J & J)

Oxford University

AstraZeneca

GlaxoSmithKline (GSK)

Novavax

Gilead

MODERNA

Lentivirus shows up in a couple of patents:Modernatx, Inc., Sars-Cov-2 mRNA domain vaccines November 4th, 2021.

The “Lentivirus” or “Lentiviral vector” is messenger RNA (mRNA) which contains the SARS, MERS, HIV 1-3 and SRV-1 Gain-and-Loss-of-Function bioweapons.

Patent: https://patents.google.com/patent/WO2021159040A2

Moderna: Delivery and formulation of engineered nucleic acids
Patent: https://patents.google.com/patent/US10898574B2

Lentivirus

cDNA (Complimentary DNA for patent eligibility using artificial genetic sequences).

Deletions (Deletions of genetic codes on particular genetic lineages in humans)

Open Reading Frame (ORF) – No stop codon (Continuous production of spike proteins of synthetic DNA)

PFIZER

Pfizer Covid-19 vaccine patent:

https://patents.google.com/patent/WO2021213945A1

Lentivirus (no mention)

cDNA

Deletions

Open Reading Frame (ORF)

JANSSEN
Janssen (Johnson and Johnson)Coronavirus vaccine:
https://patents.google.com/patent/WO2021155323A1

Lentivirus

pcDNA (plasmid cloning DNA)

Deletion

ORF

OXFORD UNIVERSITY
Oxford University: Compositions and methods for inducing an immune response:
https://patents.google.com/patent/WO2021181100A1

Lentivirus

cDNA

Deletion (See E1 and E3 Above)

ASTRAZENECA
AstraZeneca: Dapagliflozin and Ambrisentan for the prevention and treatment of covid-19
https://patents.google.com/patent/WO2021219691A1/en
Lentivirus Not mentioned in the patent
cDNA Not mentioned in the patent
Deletion Not mentioned in the patent
ORF Not mentioned in the patent

GLAXOSMITHKLINE
GlaxoSmithKline Biologicals Sa:Sars cov-2 spike protein construct
https://patents.google.com/patent/WO2021209970A1
cDNA and Deletion mentioned in the patent

ORF Not mentioned in the patent

Lentivirus Not mentioned in the patent

NOVAVAX
Novavax:Coronavirus vaccine
https://patents.google.com/patent/US20210228709A1
LentivirusNot mentioned in the patent
cDNANot mentioned in the patent

Deletion

ORFNot mentioned in the patent

GILEAD
Gilead Sciences Inc:Methods for treating sars cov-2 infections
https://patents.google.com/patent/US20210283150A1

LentivirusNot mentioned in the patent
cDNA Mentioned but seems only to refer to the formula.
DeletionMentioned for mice. Probably just for preparation purposes.
ORFNot mentioned in the patent

Other related sources:
What are Lentiviral Vectors https://biology.kenyon.edu/slonc/gene-web/Lentiviral/Lentivi2.html
Gene patents https://medlineplus.gov/genetics/understanding/testing/genepatents/
US Supreme Court ruling on cDNAhttps://www.supremecourt.gov/opinions/12pdf/12-398_1b7d.pdf

(Updated Dec. 10th, 2021)

By Dr. Ariyana Love

I compiled all the evidence we have into this article that prove Graphene Oxide, Graphene Hydroxide and other Graphene variants are in fact being injected into people by governments and Big Pharma, with intent to kill.

This evidence was discovered and proven numerous times already by independent research teams, scientists, Biotech whistleblowers and the few ethical Journalists remaining.

There’s a concerted effort by the pharmaceutical cartel funded “fact checkers,” Big Tech platforms and mainstream media, to hide the evidence and slander the people bringing this to light.

Once you go over the evidence provided here, you must take action for the safety of you and your families. Serve all war criminals participating in this COVID death jab program with a Notice of Liability for the murders they are committing. This is definitive action that any person can take, worldwide. The notices are already drafted by legal teams so why not use them and let our enemies be on the defensive. The criminals will be reminded of the Nuremberg trials, and informed that they will be brought to justice. They need to cease and desist from acting knowingly and willfully in mandating “vaccine” death jabs and enforcing them. The evidence to the danger is clear and deaths have been proven. Anyone administering or mandating these “vaccine” kill shots are doing so without Informed Consent.

COMPILATION OF EVIDENCE

On November 2nd, a prominent Professor at the University of Almeria, Dr. Pablo Campra, revealed his detection of Graphene in multiple Covid-19 “vaccine” vials, using Micro-Raman Spectroscopy. The Dr. Campra’s University of Almeria report demonstrated the detection of Graphene and Graphene Oxide in 8 samples from various “vaccine” manufacturers.

In response, Dr. Andreas Noack released a scathing video commenting on Dr. Campra’s report. Dr. Noack is a chemist and the world’s leading expert in activated carbon engineering and GRAPHENE. Dr. Noack did his PhD doctoral thesis on how to turn Graphene Oxide into Graphene Hydroxide.

The video is of crucial importance. Dr. Noack said that two of the frequency bands that Dr. Campra detected were of Graphene Hydroxide. Graphene Hydroxide (GHO) is a mono-layer activated carbon, 50nm long and 0.1nm thick (an atom layer thick). Thus, the injections contain nano-razorblades of exceptional stability, which are non-biodegrable (a fact that every chemist knows).

In effect, these nano-razorblades cut up and destroy the heart, brain and cardiovascular system. The epithelial cells become rough so things stick to them. He says that toxicologists cannot find them in a petri dish by normal methods as they do not move and they don’t expect to discover nano-sized razor blades. Moreover, any doctor who injects them with knowledge of this issue, is a murderer.

Graphene Hydroxide is a new material and toxicologists aren’t aware of it yet. This is why people are dropping dead from these lethal shots, especially athletes, Dr. Noack explains. This is a “highly intelligent poison”.

What’s even more horrifying is that if you perform an autopsy you will not find anything. This stealth weapon is even untraceable after death. The Graphene Hydroxide nano-razerblades cause people to bleed to death internally.

“Even if people don’t drop dead immediately, it cuts up the blood vessels little by little… I can say as a chemist that we are absolutely certain that the Graphene Hydroxide is in there… as a chemist, if you inject this into the blood, you know you are a murderer.”

Dr. Noack died the next day, after blowing the whistle on Graphene Hydroxide in the COVID kill shots. His wife made an announcement that it was a “brutal sneak attack”. She pleaded with us to have the courage to BELIEVE in Dr. Noack’s message about nanoscale razorblades and to ACT NOW! She said her husband is a kind soul and he did this for us, he died for all of us.

That same evening Dr. Noack released his dire warning, there was strange electrical activity at his house and an electrical outage at the same time he developed “stroke-like” symptoms. These are both indicative of Directed Energy Weapon (DEW) radiation which is what his wife thought had killed Dr. Noack. Also see link here.

Dr. Noack’s widow believes he may have been attacked by a radiation beam because he has said in the past that radiation weaponry exists and this technology can be used by “them” to take people out. She mentions the radiation in her full interview in German.

The mainstream media is ever silent about Dr. Noack’s death and his grave warning that Graphene Hydroxide is in the COVID shots. There were a few independent media publications about his untimely death and there are others who expressed belief that he was murdered, possibly by rays from afar.

Here’s Dr. Noack’s widow’s latest update in English subtitles. Some say he died of a stroke. We may never know. But what we do know is that Graphene Oxide, Graphene Hydroxide nanoscale razorblades and other Graphene variants are indeed in these shots and the pharmaceutical cartel and world governments want to inject them into every man, woman and child!

Send out this video and my article to all doctors, experts and world leaders now. Governments are already injecting 5-year-olds with Pharma’s kill shots containing Graphene Hydroxide razors. This technology will cut up their insides and delivery a gruesome, painful death to our kids!

Last year the Austrian police busted down Dr. Noack’s door and arrested him in an attempt to stop him from speaking out. The incident was recorded on camera. He was clearly a target.

Dr Pablo Campra was the first to deduce that the Pfizer serum contains Graphene Oxide flakes using Transmission Electron Microscopy in July, 2021. His techniques of detection also included infrared spectroscopy combined with optical microscopy.

Prior to Dr. Campra’s discovery, another Spanish research team named La Quinta Columna, released their discovery in June, that the COVID serums in all their variants, AstraZeneca, Pfizer, Moderna, Sinovac, Janssen, Johnson & Johnson, etc., contain a considerable dose of Graphene Oxide Nanoparticles, reported by Global Research.

Dr. Ricardo Delgado a biostatistician and founder of La Quinta Columna, discovered that 99% of the Pfizer contents are Graphene Oxide. His team was smeared by fact checkers who provided no evidence of their libelous claims.

In my article entitled, “Graphene Oxide The Vector For Covid-19 Democide,” I explain the chemical process involved in reducing Graphene Oxide to a clear liquid serum by reducing its oxygen content. By doing so, Reduced Graphene Oxide (RGO) is more lethal. So yes, it’s scientifically possible that COVID serums can be 99% Graphene Oxide.

Dr. Delgado’s team released a scientific report of their optical and electron microscopy analysis showing Graphene Oxide was found in four “Covid-19 Vaccines”. Orwell City broke the news in English. Then La Quinta Columna requested an Interim Report from the University of Almeria entitled, “DETECTION OF GRAPHENE IN AQUEOUS SUSPENSION SAMPLE”.

La Quinta Columna’s report was originallypublished in Spanishon June 28, 2021.

The problem is that this is not a vaccine, this is a dose of graphene to a person.” – Dr. Ricardo Delgado

Whitney Webb attempted a smear piece on La Quinta Columna and the University of Almeria’s discovery, where she directly attacked Dr. Ricardo Delgado’s credibility without anything substantial. Investigative Journalist Ramola D. and myself debunked Whitney’s Webb of lies.

On August 19, another research team going by the name “The Scientist Club” found Graphene in 7 prominent Biotech serums using Optical Microscope, Dark-Field Microscope, UV absorbance and fluorescence spectroscope, Scanning Electron Microscopes, Transmission Electron Microscope, Energy Dispersive Spectroscope, X-ray Diffractometer, and Nuclear Magnetic Resonance instruments to verify the serums morphologies and contents. For the high-technology measurements and the care of the investigation, all the controls were activated and reference measurements adopted in order to obtain validated results.

For obvious reasons, The Scientist Club kept their identity secret. They analyzed Pfizer, Moderna, Janssen and AstraZeneca and found a Carbon-based substrate with nanoparticles embedded, Graphene sheets and Graphene Oxide.

Undeclared metal-containing components were found by scientists in Japan, which caused the Japanese Government to halt the use of Moderna’s serums. The Japanese Ministry reported that the particles found reacted to magnets and was therefore suspected to be a metal contaminant. Graphene, Graphene Oxide (GO) and Reduced Graphene Oxide (RDO) all have paramagnetic properties.

A September, a German team revealed damning evidence of “vaccine” contaminants and autopsies linking “vaccines” to deaths.

Dr. T. made a call out to all medical professionals in this urgent announcement asking medical professionals to report magnetic phenomenon because she believes that Graphene Oxide flakes are responsible for the “vaccine”-induced magnetism that we have witnessed internationally. Dr. Andrew Goldsworthy (retired) of Imperial College London has explained the possible mechanism here.

Pfizer Whistleblower Karen Kingston revealed in August, how Graphene Oxide was hidden under a trade secret and that’s why it wasn’t listed in the patents. However Kingston explains, it is in fact the key ingredient in the Covid-19 serums.

Another Chief Scientist for Pfizer blew the whistle in November, leaking internal emails on Stew Peter’s Show from top Pfizer executives and scientists discussing how they were going to hide from the public that Graphene Oxide is in their serums.

In April 2021,Health Canada recalleda million and a half KN95 face masks containing Graphene. Children had been forced to wear these masks in Canadian schools. Health Canada compared wearing them to breathing in asbestos all day long. These poisonous masks came from China’s Shandong Shengquan New Materials Co. Ltd.

Dr. Robert Young used Scanning & Transmission Electron Microscopy which revealed Graphene Oxide in four Covid-19 trade marked serums, September 11, 2021.

Dr. Franc Zalewski also found Graphene Oxide in the Pfizer serum.

Dr. Antonietta Gatti did a recent video interview on the toxicity of Graphene Oxide Nanometallic particulates to cells. She has found them in the “vaccines”, PCR kits and face masks.

In her groundbreaking 2017 report with Dr. Stefano Montanari, Dr. Antoinetta Gatti explains Nanoparticles inside cells destroy the innate defense mechanism of cells and cause blood clots, deadly inflammation, thrombi, and multi-organ failure posed by nanometallic particulates, which are non-biodegradable and indeedbiopersistent. They can both enter cells, harm DNA, and be carried by the blood to bind with organic matter and coagulate in organs.

A Slovakian team analyzed PCR kit nasal swabs using SD Biosensor, Abbott and Nadal in a hospital laboratory from Bratislava. The team found that when DARPA’s Graphene Oxide Hydrogels come in contact with organic fluid (e.g., saliva) within a few minutes they begin to form rectangular crystal structures. These gradually grow in a fractal manner. A German research team also filmed the crystalline growth of the GO Hydrogels.

SCIENCE PAPERS & PATENTS

Several scientific papers show that Graphene Oxide is being used in gene therapy as a scaffold or platform for the delivery of mRNA into cells by way of its high electrical conductivity and ability to permeate cell membranes. The crystalline networks form in bodily fluid and replicate after injection and in the serum itself, as shown in this video of the Pfizer serum. It sure does look like nano high frequency antennas.

Graphene Oxide sheets

Scientists have developed a novel way of making carbon nanotubes at the NanoScience Center of the University of Jyväskylä, Finland, and atHarvard University, in the US.

Graphene was part of the first human genome project initiated in 2001. mRNA gene therapy Nanotech using Graphene Oxide as a vector, runs on CRISPR technology and it was developed by Pfizer, Moderna, and BioNTech, as a treatment for sick cancer patients. Due to its cytotoxicity (cell death) in healthy cells and the fact that all the animals died in the animal trials, Graphene Oxide Nanotechnology was never approved for use on Humans! Why is this technology now being used on healthy people and on children, who are at no risk of COVID?

It should be quite clear to everyone by now that the pharmaceutical cartel is using this technology worldwide, in illegal Human trials and trying to mandate their poisonous “vaccines” on everyone, with impunity.

Nanografiis manufacturing Graphene OxideNanotubes and intranasal vaccinesforCovid-19 drug delivery.

Scientists have already studied the Nose-to-Brain Translocation and Cerebral Biodegradation by intra-nasal spray, using thin Graphene Oxide Nanosheets. Make no mistake about it, nasal spray “vaccines” contain Graphene Oxide Nanoparticles.

If you’re still not convinced, here’s a main stream media article trying to pitch Graphene Oxide “flu vaccine” nasal spray as some kind of protective intervention.

Dr. Chunhong Dong is lead author of a study from the Institute for Biomedical Sciences in China where he boasts,

“This study gives new insights into developing high performance intranasal vaccine systems with two-dimensional sheet-like nanoparticles.”

Graphene Oxide has been carefully engineered as a “vaccine adjuvant for immunotherapy” and Polyethylene glycol (PEG), another highly toxic poison,is used as coating polymers. PEGs are widely used as additives in pharmaceuticals, cosmetics, and food. But PEGs come with potential life-threatening hypersensitivity reactions including anaphylaxis.

This is not a big name brand but they do mention “Carbon graphene loaded nano particles and micro-particles” in their Sars-Cov2 patent invention.

Here’s a list of peer reviewed medical studies on Graphene Oxide Toxicity and how it coagulates the blood. How much more evidence do you need to BELIEVE?

Dr. Armin Koroknay, Research director of Private Consultants and Research Institute of Zürich, analyzed the effects of COVID “Vaccination” on Blood.

Dr. Bärbel Ghitalla and her team put different brands under a microscope and found things they could not explain, but are explained in the “Covid-19 vaccine” patents.

ARE YOU A BELIEVER NOW?

If you want to support my work please consider a donation which also applies for a tax write-off.

Dr. Love’s email: metanutrients@mailfence.com

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