By Dr. Ariyana Love

(Updated Nov. 23, 2021)

Stockholm University just released a scientific horror. The “spike” protein in the COVID-19 “vaccines” is penetrating the cells of the vaccinated, reaching the cell nuclei, and impairing your cells’ 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 new discovery. 

Johnson & Johnson uses Adenovirus 26 (Ad26) in its vaccine. 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 encodes 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 a lack of oxygen in the blood. E1 gene deletion causes rapid cancer growth, Thrombosis, and the coagulation of the blood, which leads to severe blood 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, which 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 and glycoprotein -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’s syndrome, 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, and results in a gradual loss of memory, judgment, and the overall ability to function.

Here’s a study describing how you knock out 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 of 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 they kill them, unless they detoxify continuously.

The immune system of the vaxxed is deteriorating 5% each week, according to a recent UK Government study. Everyone who is vaccinated, 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 partnering with the Chinese Communist Party (CCP) to exterminate Humans.

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

Later, the WHO scrubbed it from its 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 vaccine. So this is nothing new under the sun.

Sinister shadow governments have been weaponizing nature, producing diseases through vaccine 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 they infect. Although this is not really an infection, it’s a 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 Adenovirus 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 vaccines.

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 vaccines.

Knocking out the E1 and E3 genes is necessary when transfecting across 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!

Adenoviruses 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.

49 immunologically distinct types of adenovirus 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 by 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 using E. coli bacteria. See the studies here and here.

Polio vaccines 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 vaccine.

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 vaccines, 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 vaccine-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 bacterial 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 vaccine 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 Microplasmids (parasites, transgenic Hydras, and bacteria) and reverse the coagulation cascade, which leads to blood clots.

Please visit my website at www.drlove.live to contact me or to schedule a health consultation.

You can also visit my online shop at www.drlovesapothecary.com to purchase protocol supplements.