by Dr. Ariyana Love

For humanity.

I will be updating this document periodically.

Because many are unaware, I was the first person in the world to read the Covid-19 “vaccine” patents, document them and report my findings on Stew Peters Show. This was back in October 2020, in the wake of Event 201, aka “Covid-19”.

By January 2021, I had succeeded in detoxing my first client from two Pfizer jabs. Since then, I have helped hundreds of clients and thousands of people with my detox protocols.

Here is the “First Ever” protocol to emerge in the west, from Finland.

  1. ASEA Redox Molecules
  2. Stemtech
  3. Pine Needle Essential Oil
  4. Parasite Detox
  5. Microbiome Protocol
  6. Blue Green Algae

ASEA Redox Molecules

ASEA redox molecules boost glutathione levels to between 500-800% and balance all bodily functions. Read more about ASEA redox molecules and order here: ASEA Redox Molecules Anti-Aging Power.

ORDER HERE: Visit the ASEA homepage of Dr. Ariyana Love.

Stemtech

Our adult stem cell production is the second most vital function that we lose when the aging process begins, leaving every adult deficient in the ability to heal from bodily injury after the loss of adult stem cell function.

Adult stem cells are our body’s master cells. They are necessary for the self-renewal and self-repair of damaged cells, tissues and organs. Prolonged Mitochondrial Fatigue due to Reactive Oxygen Species (ROS) from GON further suppress our adult stem cell production.

After years of scientific lab research, Stemtech has isolated key super nutrients that reactivate adult stem cell production. Using all three Stemtech products gives you a 53% increase in adult stem cell production, reducing inflammation and enabling the body to heal and bounce back rapidly after cellular injury. Using Stemrelease3 alone will increase adult stem cell production by 20%.

Stemtech’s powerful antiaging meta nutrients super boost the immune system, restore Ph balance, and empower swift regeneration of cells and organs from bodily injury. The rapid rate of absorption of ASEA redox molecules effectively deposits Stemtech’s vital nutrients directly into your cells for immediate absorption and usability. Redox molecules absorb into every cell of your body in just 5 minutes, driving oxygen in and nanotech out, while repairing your DNA and supercharging your immune system. This rescues mitochondria from fatigue and pulls the body out of ROS.

ORDER HERE: Visit the Stemtech homepage of Dr. Ariyana Love.

Pine Needle Essential Oil

Pine needle oil is the most effective natural medicine that kills genetically modified mRNA parasites and all parasites. Pine needle oil surrounds all parasite varieties and suffocates them to death.

Unlike Ivermectin, Pine needle oil can be used continuously throughout your detox, as it’s classified and used by our bodies as an essential food.

Pine needle oil is a treatment against influenza A, a potent antibacterial, antifungal and a natural antibiotic. It’s an effective blood thinner, anticoagulant, antimalarial, antitumor, antimicrobial, anti-inflammatory and a powerful antioxidant with 5x the amount of vitamin C as oranges.

Pine needle oil is one of the top meta nutrients known to man, super boosting immunity. Pine oil absorbs into every cell of your body in just 20 minutes, conducting targeted cellular repair.

Pine oil super nutrients are unique because they bypass your nervous system and treat nerves directly. Pine oil remedies depression, chronic PTSD and reverses the memory of trauma in your cells. There is no replacement for pine needle oil which is essential now in every protocol, in my humble opinion. If you cannot find pine, you can also use Spruce, Douglas Fir or Ceder.

Listen to my podcast on the healing remedies of pine needle essential oil.

ORDER HERE: RED PINE NEEDLE OIL

Parasite Detox

I use Young Living Essential Oils with my clients for parasite detox. I use either Young Living Scots Pine needle essential oil or Dr. Robert Young’s Red Pine needle oil for parasite cleanse. High quality essential pine needle oil is the most effective way to thoroughly detox parasites. Turpentine 100% Pure Gum Spirits works very well also for the initial die off. The entire pine tree is edible, highly medicinal and classified as an “essential food”.

Microbiome Protocol

My Microbiome protocol blend is critical for stopping the replication of Alhydrogel, Inhalation Anthrax and Injection Anthrax and E. coli poisoning. Thus, it remedies GI and digestive issues, along with the parasite detox.

Young Living essential oils

We are all being exposed to genetically modified AI parasites. The highest quality essential oils are necessary for parasite detox because essential oils bypass the digestive process. They absorb through the tissues within minutes, traveling into your interstitial fluids (fluid between cells) making the vital nutrients accessible to the cells throughout your entire body. You cannot replace the quality of Young Living oils with any other company.

You must enroll as abrand partner” in order to purchase products. The starter kit is optional but you must enroll to be able to order products. You will need my brand partner and sponsor number which is # 37904828.

Visit the Young Living website of Dr. Ariyana Love for additional essential oils.

ENROLL HERE: YOUNG LIVING ESSENTIAL OILS

Blue Green Algae

Blue Green Algae from Klamath Lake Oregon, is the most nutrient-dense food known to man and has miraculous healing properties. It contains all the vitamins and minerals our bodies need. It also exhibits potent antiviral activity against “HSV-1, HSV-2, human cytomegalovirus and influenza A virus”, inhibiting the initial stage of infection including the binding and internalization processes.

Blue Green Algae inhibits the initial stage of “infection” when poisoned with Covid-19, including the binding and internalization processes. It exhibits potent antiviral activity against “HSV-1, HSV-2, human cytomegalovirus and influenza A virus” (nanotech replication).

Blue Green Algae is antiparasitic, antibacterial, antifungal, and more. This single-celled miracle food works like our mitochondria to surround heavy metals and chelate them most effectively, while simultaneously repairing damaged cells. Blue Green Algae is another powerful anti-inflammatory that is rich in chlorophyll and chlorophyll prevents infection. Blue Green enables red blood cells to regenerate and this is critical because Covid-19 technology destroys red blood cells.

Blue Green reverses cancer, depression and thyroid issues while activating adult stem cell production.It stimulates serotonin production significantly, reversing depression. Blue Green reverses cytotoxicity and boosts glutathione, which is our body’s master antioxidant.

Harvesting technology

There are two kinds “Blue Green Algae”, so please do not be confused. One is toxic, and the other is super healing food. Spirulina and chlorella cannot replace Blue Green. The harvesting technology used to extract Blue Green Alage determines the percentage of nutrients retained, so knowing the company you buy from is very important.

Green Earth Naturals Best Blue Green uses a superior harvesting technology that retains 95-98% of the vital nutrients in Blue Green Algae. Clause: I do not endorse their digestive enzymes. I only recommend the Blue Green Algae powder.

ORDER HERE: BLUE GREEN ALGAE (recommended source)

Vitamins

Melatonin (organic plant based)

Quercetin (Source yourself: inflammation reduction & antioxidant detox)

Vitamin D3 (10,000 IU daily as per Dr. Zev Zelenko’s recommendations)

Vitamin C Acerola

I endorse and guarantee the quality of all products from ASEA, Stemtech, Young Living, and Ph Miracle Products.

There is no need to use zinc so long as you’re using ASEA redox and/or sodium chlorite, which are both cellular drivers.

I used 1-5 natural medicines and supplements to detox people since September of 2020. I added my Microbiome Protocol after discovering that the Covid-19 “vaccine antigen” is an enhanced form of Anthrax. PLEASE READ: BREAKING: Anthrax Is The COVID-19 “Vaccine Antigen” And It’s Aerosolized!

SCHEDULE A CONSULTATION

If you would like my detox and customized protocol support, please schedule a consultation with me here: https://calendly.com/drariyanalove.

“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

Follow Dr. Robert Young’s work here.

Follow Dr. Ariyana Love’s Telegram channel here.

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, ND

The samples pulled out of the veins and arteries of COVID vaxxed corpses shocked the world and exposed that something more than just “vaccination” is taking place.

In my latest interview with Stew Peters entitled, Human Umbilical Cord Being Injected In Kids: Tissue Scaffolding Technology In Covid Jab, I revealed in detail what the strange “blood clot” samples found by embalmer Richard Herschman, actually are. The story was first aired by Dr. Jane Ruby on Stew Peters Show in January and was recently examined LIVE on air by scientist Mike Adams in the InfoWars studio, in a worldwide medical bombshell.

The samples pulled out of the veins and arteries of COVID vaccinated corpses shocked the world and exposed that something more than just “vaccination” is happening with the COVID vaxx. The fact that mainstream media did not pick up on this story is more proof we’re in dystopian times.

Embalmer Richard Heirschman’s samples published by Dr. Jane Ruby
Embalmer Richard Herischman’s sample published by Mike Adams of Natural News

These images show synthetic tissue is being grown inside humans from the COVID vaxx. This is most likely the cause of “Sudden Adult Death Syndrome.”

Please see the following studies:

Tissue-Engineered Blood Vessels (2005)
Researchers Grow New Blood Vessels In Just Seven Days (2014)
Arterial reconstruction with human bioengineered acellular blood vessels in patients with peripheral arterial disease
From Autologous Flaps to Engineered Vascularized Grafts for Bone Regeneration

China constructing blood vessels (2020)

Bioactive polymeric scaffolds for tissue engineering

Below are images of artificially grown blood vessels by lab scientists.

Artificial blood vessels
Artificial blood vessels

There are synthetic and natural polymers. They are elastic and made from these five different materials:

  1. Polyester polymers PLLA and PGA are among the most commonly used biodegradable synthetic polymers.
  1. Silk fibroin protein is extruded from insects and worms. It has biocompatible properties with the human body and ossess relatively high tensile strength.
  1. Collagenis used for bone construction.
  1. Hyaluronic acid (HA) is a form of hydrogel material for both hard and soft tissue construction.
  1. Chitosan is biodegradable polysaccharide that comes from chitin via chemical hydrolysis. It’s used in a gel, sponge, or fiber form.

I believe the below image from the embalmer and published by InfoWars, is a Silk fibroin tissue construct.

Certified embalmer Richard Hirschman’s sample – infoWars

NANOWIRES

Nanowires are being used for the hybridization of humans. Pharmaceutical companies and world governments are attempting to grow artificial tissue inside humans, using organic matter from cross-species genomics. They appear to be trying to merge humans with electronic devices for internal tracking and remote control.

Nanowires are superconducter batteries used for tissue scaffolding inside the human body. I wrote about tissue scaffolding technology in December of 2021, in my article entitled, Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State.

See studies and patent examples:

Nanowires

Nanowire arrays for neurotechnology and other applications

Internalization of ferromagnetic nanowires by different living cells (2010)

Hydrophobic copper nanowires for enhancing condensation heat transfer

Rotational Maneuver of Ferromagnetic Nanowires for Cell Manipulation

Internalization of ferromagnetic nanowires by different living cells

Ultrathin gold nanowires to enhance radiation therapy

The presence of gold nanowires cause elevated lipid peroxidation and intracellular oxidative stress under radiation. This can literally fry people from the inside using microwave frequency. This could explain why vaxxed persons are reporting torture by electrical activity in their head and their body.

I believe the image below that was shared by Mike Adams on InfoWars, shows a gold Nanowire.

Gold Nanowire – InfoWars

This study entitled, Macroporous nanowire nanoelectronic scaffolds for synthetic tissues, reveals electrical sensors made from silicon which are lab-on-a-chip pharmacological platforms and hybrid 3D electronics-tissue materials for synthetic biology and tissue construction for inside the human body. These are planar devices used to probe electrical activity near the surface of the heart, brain and skin, acting as transmitters, transistor and receivers.

“This is nanoelectronics throughout biomaterials and synthetic tissues in 3D using macroporous nanoelectronic scaffolds. They are using silicon nanowire field effect transistor (FET)-based nanoelectronic biomaterials, given their capability for recording both extracellular and intracellular signals with subcellular resolution.”

Nanowires are also called detectors, metal electrode or carbon nanotube/nanofiber or NanoES. They are implantable microelectrodes, nanoscale semiconductors and flexible/stretchable electrodes. The sensor network is flecible, macroporous and 3D. They are used to construct artificial tissue with embedded nanoelectric sensory capabilities.

Below is an image of Nanowires.

Nanowires

ORGANOIDS

Organoids are used to construct a new brain inside humans, for mind control. Organoids and transgenic hydras are being used to build a new neural network inside the body. The studies showing this can be found in my article entitled, Pharma Exposed! Autism Spectrum Disorder (ASD) Is Targeted Gene Deletion!

Also see: Transgenic Hydras & Parasites A Biological Weapons System For Rapid HumanCloning.

MICROSPHERES

I wrote about Microspheres, Microbubbles and Microbeads delayed release technology in my article entitled, Quantum Dots, DNA Barcoding, Nano-Razors & The IsraeliState.

Microspheres are in the COVID shots. They are also used for tissue engineering and scaffolding, simultaneous drug delivery and for growing cells inside the human body. The technology is externally controlled by EMF transmission. Microspheres can release their payload, weeks, months and even years later.

This tech was developed with the purpose of destroying cancerous tumor cells and now it’s being misused for the Democide of humanity.

The study entitled, Nanostructured injectable cell microcarriers for tissue regeneration, demonstrates that nanostructured microspheres include nanocomposite and nanofibrous microspheres which have been employed as cell carriers for tissue construction. They produce cell attachment and growth, promote cell-carrier interactions and facilitate stem cell differentiation for target tissue construction inside the human body.

A study entitled, PHBV Microspheres as Tissue Engineering Scaffold for Neurons, demonstrates that Polymeric microspheres are being used to grow artificial neurons inside humans.

A study entitled, Breathing life into engineered tissues using oxygen-releasing biomaterials reveals that the artificial cells feeds on your blood to grow and survive! This may explain the strange blood clots we’re seeing in vaxxed injured persons. Human umbilical vein endothelial cells are used to grow the artificial cells.

This study entitled, Generation and differentiation of microtissues from multipotent precurser cells for use in tissue engineering, reveals that Microspheres use unrestricted somatic stem cells from human umbilical cord blood.

This technology is truly vampiric and relies on human baby tissue in order to be grown inside humans. This should not be injected into anyone, especially not children!

——————————————————————————————————

Daniel 2:43 (KJV)

(43) And whereas thou sawest iron mixed with miry clay, they shall mingle themselves with the seed of men: but they shall not cleave one to another, even as iron is not mixed with clay.

By Dr. Ariyana Love, ND

In my latest interview with Stew Peters, I brought scientific studies revealing that Autism Spectrum Disorder (ASD) is caused by gene deletion in the brain, specifically in the frontal cortex.

The article I referenced from Nature entitled, Epigenetics and cerebral organoids: promising directions in autism spectrum disorders, explains that the inactivation of the X chromosome in the brain is what causes Autism Spectrum Disorder (ASD).

The three regions of the brain being targeted are the temporal cortex, cerebellum, and prefrontal cortex, especially the frontal lobe. These regions were shown to have lower methylation levels of the X chromosome with ASD. The study specifies that X chromosome deletion occurs by “epigenetic dysregulation” (gene deletion) and “DNA methylation” (genetic coding).

“Although the epigenetic mechanisms involved in autism are not yet fully understood, there are findings suggestive of genome-wide dysregulation and epigenetic alterations in ASD (Autism Spectrum Disorder). These studies point to DNA methylation (gene editing) as a likely contributor in the development of the disorder.

There are certain syndromes that have been linked to ASD. DNA methylation in connection to imprinting and X-chromosome inactivation (gene deletion) could be relevant to the field of ASD research. X-chromosome inactivation is a process in which one of the copies of X chromosomes is inactivated and this is also achieved through DNA methylation. It might be associated with autism, as inactivation or removal of inactivation could lead to genetic aberrations.”

Targeted deletion of the X chromosome in other areas of the brain result in ASD conditions such as Angelman syndrome and Prader–Willi syndrome. Deletion of the X chromosome in females causes Turner syndrome which induces mental retardation, developmental delay and effects social reciprocity and communication, a condition of ASD.

Another study entitled, DIA1R Is an X-Linked Gene Related to Deleted In Autism-1 confirms X chromosome deletion explaining, “A DIA1 deletion coincided with a classical autism diagnosis.”

Autism rates have exponentially risen over the last two decades and continues to sharply rise. Belfast, Ireland just reported that one in 14 children have ASD!

DELETION SYNDROMES

In an interview with Maria Zeee, Attorney Todd Callender stated:

“The 1p36 gene deletion is a congenital disease — you’re born with it — and yet that was the number one serious adverse event, and if you look up the symptomology for that, it’s the elimination of your frontal cortex. Your thinking part of your brain, your decision-making part of your brain, is the number one serious adverse event listed by Pfizer.”

Previously, we were told that deletion syndromes as well as the 1p36 Deletion Syndrome, are rare phenomenons. However, now it’s “the most common human disorder” resulting from the deliberate deletion of the X chromosome in the frontal lobe. Not only does the 1p36 gene deletion cause mental retardation but it also causes genital abnormalities in males and females, affecting fertility.

Another study from 2020 reveals that 25% of people affected by “Covid-19” are loosing the electrical activity in the frontal cortex of their brain. Many of my clients, friends and associates have been reporting “brain fog.” Could this be an adverse reaction from transmission (shedding) of vaxxed persons, caused by targeted gene deletion of the frontal lobe?

In addition, the the authors suggest that the infection may have aged people cognitively by around 10 years!

In her recent report, Dr. Stephanie Seneff, a Senior Research Scientist at MIT’s Computer Science and Artificial Intelligence Laboratory in Cambridge, outlined the extensive neurological damage such as PRION, induced by the mRNA “vaccines.” In particular, she highlighted how the mRNA technology is rapidly aging people.

— To view, copy/paste this report link into your url: file:///C:/Users/metan/Desktop/20220612_MD4CE_Dr_Stephanie_Seneff%20-%20Copy.pdf

By the way, the E1 gene is on the X chromosome genetic lineage. I previously documented how pharmaceutical “vaccines” are deleting the E1 gene in my article entitled, EPIGENETICS: Vaccines Are Deleting Human Genes & Transfecting Cells WithEbola/Marburg.

It begs the question. Have pharmaceutical companies been intentionally inducing Autism by deleting genetic codes in the human brain through their vaccination programs? The only way the deletion of the X chromosome is possible is through the use of mRNA nanotechnology.

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.

Source: The Expose (February 24, 2022)

By Rhoda Wilson

In his latest set of slides of blood samples taken from both “vaccinated” and unvaccinated people, Dr. Philippe van Welbergen demonstrated that the graphene being injected into people is organising and growing into larger fibres and structures, gaining magnetic properties or an electrical charge and the fibres are showing indications of more complex structures with striations.

He also demonstrated that “shards” of graphene are being transmitted from “vaccinated” to vaccine-free or unvaccinated people destroying their red blood cells and causing blood clots in the unvaccinated.

Dr. Philippe van Welbergen (“Dr. Philippe”), Medical Director ofBiomedical Clinics, was one of the first to warn the public of the damage being caused to people’s blood by Covid injections by releasing images last year of blood samples under the microscope.

Atthe beginning of July 2021,Dr.Philippe, was interviewed on a South African community channel,Loving Life TV. He explained that when his patients started complaining about chronic fatigue, dizziness, memory issues, even sometimes paralysis and late onset of heavy menstruation (women in their 60s upwards), he took blood samples. Their blood had unusual tube-like structures, some particles which lit up and many damaged cells. Few healthy cells were visible. Until three months earlier, he had never seen these formations in blood. We now know these tube-like structures are graphene.

Since then, Dr. Philippe has beena regular guest onLoving Life TV: blowing the whistle on the experimental Covid injection roll-out; providing updates on the increasing damage being done to blood by the experimental Covid injections over time; and, giving updates on the Covid situation in the UK and South Africa.

On 12 February 2022, Dr. Philippe returned again toLoving Life TVto release images of his latest slides of blood samples.The live streamwas lengthy soLoving Life TVseparated it into two parts.

Part Oneis a discussion including answers to the audience’s questions.

InPart Two, Dr. Philippe presents the images of his latest blood slides and explains what the images are showing. He discusses nearly 100 blood slides from both “vaccinated” and vaccine-free patients. His slides show that vaccine-free patients have been “infected with vaccine toxins through shedding.”

Below is a short clip from Part Two courtesy of The Timeline Post channel on Telegram.

Below is an image of typical healthy red blood cells as seen with a microscope, what blood should look like. There is no coagulation or foreign objects in it.

The next image is of a person who has been injected with the experimental Covid drug. The blood is coagulated, the misshapen red blood cells are clumped together.  The cell encircled in the image is a healthy red blood cell, one of the few in the image, sitting alongside the graphene fibres.  You can see the size of the graphene fibres in relation to the size of a red blood cell. Fibres of this size will block capillaries. You can also see the graphene fibres are hollow and contain red blood cells.

The image below is of a blood sample from a vaccine-free, or unvaccinated, three-year-old child.  It shows pieces or “shards” of graphene that “are the result of shedding,” in other words the graphene has been transmitted from “vaccinated” parents to their unvaccinated child.

The image below is of a blood sample from a vaccine-free, or unvaccinated, three-year-old child.  It shows pieces or “shards” of graphene that “are the result of shedding,” in other words the graphene has been transmitted from “vaccinated” parents to their unvaccinated child.

Below is the image of a blood sample from an eight-year-old unvaccinated child whose blood has been contaminated and destroyed by the transmission of graphene from those around him/her who have had a Covid injection.  The child’s right arm and upper right leg are basically paralysed, the child is unable to lift his/her right arm and the thigh is not functioning properly.

Dr. Philippe’s presentation is truly eye opening and horrifying – a must watch, especially for those who proclaim Covid injections are “safe” and are insisting people be injected. The Covid injections are weapons of genocide and how the people who have designed them are still walking free is incredible.

You can either watch the presentation below or on Loving Life TV HERE.

Source: The Expose

Follow The Expose here

Please see: Graphene Oxide The Vector For Covid-19 Democide

Also see: TRANSMISSION with Dr. Ariyana Love

By Dr. Ariyana Love

(Updated January 11, 2022)

The U.S. Army just announced their new creation of a Spike Ferritin Nanoparticle (SpFN) “vaccine”, claiming that it works “against all existing COVID & SARS variants”. Without animal testing or safety studies, Human trials are already underway.

The U.S. Army published a series of preclinical studies claiming the Spike Ferritin Nanoparticle serum “protects against heterologous challenge with B.1.1.7 and B.1.351 virus variants” during an animal trial. This is key to understanding what they’re really doing with these death jabs.

“B.1.1.7” and “B.1.351” are literal genetic lineages that contain your God-given genetic information. Heterologous challenges result from cross-species genomics. When you delete genes and code Human cells with insect DNA (Luciferase) and monkey DNA, bad things happen. It’s called genetic mutation.

The official narrative explains that the B.1.1.7 Alpha variant of SARS-CoV-2, the supposed “virus” that causes COVID-19, has turned up in the UK and the B.1.351 Beta variant in South Africa. Then there’s the B.1.1.529 Omicron variant which is new on the scene. Now I’m going to explain to you how you’re being fooled because first they fool you then they rule you.

The CDC website mentions the “variant of concern (VOC), lineage B.1.1.7 is also referred to as VOC 202012/01 or 20I/501Y.V1”. Another page of the CDC website says about the B.1.1.7 variant, “This variant has a mutation in the receptor binding domain (RBD) of the spike protein at position 501, where the amino acid asparagine (N) has been replaced with tyrosine (Y). The shorthand for this mutation is N501Y”.

The key word in that quotation is REPLACED.

The Bullfrog

Look up N501Y and you find that it’s a genetic mutation resulting from reverse genetics (cloning). Reverse genetics involves directed gene deletions and point mutations (site-directed mutagenesis) to create null alleles (non-functional); which is gene knockouts. These gene deletions lead to permanent loss-of-function.

CRISPR-Cas9 – technology is raping your cells’ genome and cutting it at a specific location to allow genes to be removed and new engineered sequences to be inserted using RNA interference to permanently silence genes. Genetic knockdowns are typically temporary whereas genetic knockouts are permanent.

Moderna and other pharmaceutical bioterrorists researched extensively the knockout of genes in regards to “curing cancer” and what the reduction of amino acid asparagine (N) causes. The CDC says the amino acid asparagine (N) has been replaced with tyrosine (Y). When you knockout genes, the protein associated with that gene stops being produced by your cells. In this case it’s the amino acid asparagine (N) that has been replaced with tyrosine (Y) which causes rapid cancer growth. They want you sick and dying.

Gene deletion is also a behavioral modification that decreases your intelligence. It also serves to enhance receptor binding. Doctors must pay attention to this information.

The N501Ymutationis being induced by gene deletion, to cross the species barrier so that animal diseases (monkey disease) can create infection in Human cells that would not naturally occur. Since animal diseases do not infect Humans, cloning is necessary.

The UK Government says the “VOC-202012/01 variant includes 23 changes in the “virus” with eight mutations (changes) in the outer “spike” protein; nine changes that alter the amino acid sequence of proteins elsewhere in the virus genome, and six changes that do not alter the amino acid sequence of proteins elsewhere in the virus genome”.

What they are really talking about is YOU. Since viruses are still a theory and have never been proven to exist, governments and the pharmaceutical cartel are using the word “virus” to deceive the medical community and divert our attention away from their Bioterrorism. They want us to believe that a boogey virus mysteriously jumped from bats to Humans when actually they’re making changes to the Human genome.

This study confirms that SARS-CoV is nothing but “S glycoproteins” made using an unnatural genetic sequences that fools your cells into thinking it’s natural so your body will not reject the biohacking technology.

The Spike Ferritin Nanoparticle SpFN WO2021178971A1 patent, also confirms that the SARS-CoV is an “glycoprotein S” which is the “spike protein”.

So there you go, mystery solved. The infamous “spike protein” is not a “spike” protein from a “virus” after all. The glycoprotein S is a chimeric Bioweapon.

The SpFN patent also contains the transfection agent HEK293T/17 which is Human embryonic kidney DNA. It’s a chimeric “pcDNA” for cloning.

Thermo Fischer is using a “pcDNA cloning kit” which also does gene deletion.

The SpFN patent also contains HIV-1 which is patented and owned by the treasonous, mass murdering, Genocidal Anthony Fauci. It also has Luciferase (insect DNA) for tracking your every move. Oh yeah… and the patent confirms it came from Wuhan, China!

Aluminum Hydroxide is also listed in the SpFN patent and Aluminum Hydroxide is made from Graphene Oxide. They call it “Alhydrogel”. So… Graphene Oxide is irrefutably in the SpFN Bioweapon shots!

It gets even more disgusting. They’re using bullfrog DNA to create their chimeric glycoprotein “S”.

Who wouldn’t want to be transfected and cloned with bullfrog? Because if you don’t accept their Franken-vaxx, then you’re a racist… against the bullfrog species!

GENE DELETION

Studies show that the B.1.1.7 “variant” is directly caused by gene 69-70 deletion in Humans. The B.1.351 “variant” is directly caused by gene241–243 deletion.

The CDC openly admits that the Omicron variant is the result of an “S gene drop out” caused by “gene 69-70 deletion”.

The World Health Organization says that the S gene is not present in the Omicron variant. In its report titled “Classification of Omicron (B.1.1.529): SARS-CoV-2 Variant of Concern“, the WHO’s Technical Advisory Group on SARS-CoV-2 Virus Evolution (TAG-VE) confirmed that the RT-PCR kits which are designed to target the S gene, detect a complete dropout of the S gene.

Thermo Fisher’s Genetic Sciences Division revealed that the B.1.1.7 variant is the result of gene mutation caused by the gene deletion of the “S gene”. Thermo Fisher explains that the “S gene” is a 69-70 deletion. Thermo Fisher admits that gene deletion mutations is the cause of all SARS-CoV-2 variants, Lambda, Alpha, Beta, Gamma, Delta, etc.

Are you catching on? The “S” gene is the glycoprotein S Bioweapon, an artificial genetic sequence that’s being coded into Human cells (transfection/cloning) after gene knockout.

On their website Thermo Fisher also admits:

“The Omicron variant has been found to include the 69-70del mutation of the S gene, first identified as a mutation in the Alpha variant. This mutation causes a dropout of the S-gene target in results from widely used TaqPath COVID-19 Detection Kits. An S-gene failure does not mean a result is negative, only that the S gene was not detected. Multiple public health organizations have noted that this pattern of detection (i.e. S-gene dropout) can be used as a marker for this variant, pending sequencing confirmation.”

So there you have it. The PCR kits target genes for gene deletions and monitor the cloning progress.

All Covid vaxx patents mention gene deletion. Both Pfizer and Moderna claim their serums “protect against” the variants. The Moderna patent states it’s death jab is “folding proteins”. The folding of proteins induces genetic mutations.

The Pfizer patent directly states that it’s serum is deleting genes 69-70 and 242-244. So these lying bastards are not “protecting” against anything. They are inducing the scary variants through gene deletion.

Do not drink their poison.

The Pfizer vaxx patent also mentions the N501Y mutation due to but not limited to 69-70 gene deletions. Remember, 144 gene deletion causes rapid cancer growth.

Pfizer patent WO2021213945A1

Thermo Fisher owns the patent to a PCR kit that “targets genes”. The PCR kit is also a marker to “test” for gene deletions to determine if the jabbed are patent eligible.

Thermo Fisher sells the Microbeads used in the death jabs and markets them as Dynabeads and SPIONs. Then they have a PCR kit to “test” how their cloning project is going.

Cloning any species results in mutations that are unpredictable, as I previously documented in my articles here, here and here.

CONCLUSION

Variants are caused by gene deletion from fake vaccines and fake tests. Stop complying to your Democide and Mark of The Beast enslavement.

Serve the war criminals (anyone pushing the death jab) with Notices of Liability.

Contact me or book a free consultation and I will help you design a detox protocol that fits your needs and your budget, to remove the biological poisons we are being bombarded with. Do not loose hope because there are solutions to save and protect your health.

(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