Naturopathic Doctor - Dr. Ariyana Love

MEGA BOMBS! GMO Parasites Are The mRNA Vectors!

Posted on October 16, 2022March 3, 2025 by Ariyana Love

“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.

MODERNA

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

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

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.

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.

OXFORD

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

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.

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.

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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.

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Snake Venom Key Ingredient In “Covid-19 Vaccine” Patents

Posted on April 14, 2022March 3, 2025 by Ariyana Love

By Dr. Ariyana Love, ND

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

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

SNAKE VENOM PATENTS

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

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

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

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

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

THE SPIKE PROTEIN

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

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

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

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

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

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

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

CROTOXIN

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

ORGANOIDS

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

MONOCLONAL ANTIBODIES

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

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

Please read: Monoclonal Antibodies Is Experimental Gene Therapy – PatentReview

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

NANOBODIES

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

ANTIDOTE

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

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

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

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

Also, follow my Telegram channel here.

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

Posted on February 26, 2022March 2, 2025 by Ariyana Love

By Dr. Ariyana Love (ND)

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

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

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

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

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

PATENT REVIEW

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Please see: Covid-19 Patent Horrors

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

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

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

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

MARKER GENES & mRNA

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

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

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

Monoclonal antibodies is a mRNA nanotechnology vaccine.

IMMUNE SYSTEM DESTRUCTION

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

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

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

Posted on December 24, 2021March 2, 2025 by Ariyana Love

By Dr. Ariyana Love, N.D.

*EMERGENCY MEDICAL WARNING*

*ATTENTION HUMANITY*WORLDWIDE ALTERT*

La Quinta Columna just told us the extermination of Humans could be complete in a few months. My ears are still ringing but this information is solid and sound! God be with us all!

After 20,000 hours of research by scientific teams, the University of Almeria and The Fifth Column release a comprehensive report outlining the mechanism of Telephoresis and 5G, a Bluetooth connectivity both found in patents and science labs in Europe.

Evidence proves that Covid-19 is induced by Graphene Oxide, a bioligical weapon.

Source: La Quinta Columna