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.

By Dr. Ariyana Love

Covid-19 is a biological and technological weapon system using self-replicating, programmable nanotechnology with synthetic modRNA poisons. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” because that’s medical science. But what if the Covid-19 vaccine antigen is ANTHRAX?

“…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.”

The first Anthrax was a biological weapon developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene“ into the highly toxic Bacillus Anthracis bacteria. This means that advanced technologies such as Cross-Species-Genomics capability was acquired by the government before 1950 when a lethal bacteria and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax.

Russia’s Anthrax could be treated with antibiotics even several days after exposure and thus it met the requirements under the Biological Weapons Convention. Being the bioweapon of choice, NIH funded Anthony Fauci increased Anthrax’s lethality. Russia’s Anthrax was genetically attenuated by the NIH before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more.

According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast).

Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.”

The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks but we already know that the D.O.D spearheaded this “Covid-19 vaccine” Democide.


Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides


In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Both have just been administered to the world population through inoculations, PCR swabs and aerosolization and self-replication.

Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014 creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH, also in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously in 2014, China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study admits to severe side effects.


PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses


The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in “vaccines” under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare.

In March of 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more.

Ebola is used in the J&J and Sinovax jabs while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. The H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs!

Here’s how they did it. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop it from replicating inside the human body due to it being antibiotic resistant.

The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquitoes which is part of DARPA’s weaponized insect project called The Sentinels.

Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax.

Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

SPIKE PROTEIN IS AEROSOLIZED ANTHRAX!

There’s 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.”

The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine“.

“The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.”

In layman’s terms, the poisonous Anthrax “antigen” is being used in the genetic modification of the human genome and it’s literally being encoded into the genome, after knockouts (deletions) of the genome.

The molecular basis of Anthrax “vaccines” contains “spores and DNA plasmids.“ This is a targeted weapon system. The following quote about the Anthrax “protective antigen” is particularly revealing:

“PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).”

Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want.

Luciferase is insect DNA and that’s going into the genome. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery (aerosolization), the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized.

This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic.

This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality.

ALHYDROGEL

The hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health.

According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is Alhydrogel. The Alhydrogel is infused with 750 μg of aluminum, making it magnetic. In the Alhydrogel invention, Anthrax was fused together into this nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”.

Again in layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death.

Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network, which is what I believe some eugenicists were trying to achieve.

Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There’s many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system.

This Alhydrogel patent demonstrates its use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability.

It begs the question, where do venereal diseases come from? But I digress.

This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades however, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel.

“Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA.

So, both nanoparticles and Anthrax have been used in vaccines for decades already, without Informed Consent of the public.

Alhydrogel was improved and transformed into the Nanoalum adjuvant.

Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor.

The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites.


Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector!


ANTHRAX SYMPTOMS AND TREATMENT

Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and swabs which contain delayed release technology that contains a military weapon system.

Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements.

Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans it’s EXTREMELY TOXIC.


Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review


They also say the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a complete disaster. U.S. Army statistics that were never published show the Anthrax “vaccine” induces cancers.

The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis? Anthrax also coagulates the blood. Read more here and here.

“Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.”

Anthrax also causes a person to hemorrhage. So this explains all the excessive bleeding people experience after Covid-19 injections and from aerosolized exposure. In other words, shedding by transmission. Inhalation Anthrax.

Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by https://pmc.ncbi.nlm.nih.gov/articles/PMC3124019/proinflammatory cytokine signaling and histological lesions in the spleen.

Anthrax has been tested on the public already. During 9/11 Anthrax spores were intentionally released into “some environments” in NYC, according to the NIH. The FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI.

Heroine users in Europe have been tested on with Injection Anthrax.

Our skies are sprayed with smart dust and chemicals daily. Our governments have launched all out war against their constituents. We are being poisoned in a myriad of ways so please keep this in mind:

“Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by Whole Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.”

TREATMENT

If you have been inoculated with Covid-19, or PCR swabbed and you are suffering from heart pain and other severe symptoms, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated” then you may have been exposed to Inhalation Anthrax.

Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. If you have been exposed to Inhalation Anthrax, you will feel hot and very flushed, similar and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning.

Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need a good doctor with complete protocols.

I have been successfully detoxing people from the Covid-19 bioweapons for two years. I have a complete protocol for Anthrax poisoning. If you would like to schedule a consultation with me, please do so through my online booking system.

If you would like to donate to my research, please do so here.

By Dr. Ariyana Love

(Updated Nov. 23, 2021)

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

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

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

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

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

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

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

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

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

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

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

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

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

Knocking out the E2B gene caused sterilization in male mice.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Later the WHO scrubbed it from their website.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

PLEASE SEE: DR. LOVE’S DETOX PROTOCOL

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