Varicella Chickenpox Vaccine Contains Human Fetal Tissue and mRNA Nanotech

"Things come apart so easily when they're held together with lies" - Dorothy Allison

By Dr. Ariyana Love

All major biotech companies have a Varicella patent, claiming to be a chickenpox vaccine, including Pfizer, Moderna, Novavax, Merck, GlaxoSmithKline, and more.

Medical doctors receive a private insurance administration fee of approximately $16.62 to administer the Varicella vaccine, while for Medicaid, the average kickback is around $9.45. Most medical doctors do not bother to read vaccine patents, and if they did, many of them would voluntarily surrender their license and find another profession. Let's dive into the reasons why.

The Varicella vaccine is on the childhood vaccine schedule in many countries, including the US and Canada. The CDC recommends that children receive two doses of the varicella vaccine, with the first dose at 12 to 15 months and the second at 4 to 6 years of age. It appears to be a harmless vaccine, but there's a very sinister plot behind it.

Medical doctors routinely recommend the Varicella vaccine for children. However, the safety of this inoculation is disputed due to the severe adverse reactions it induces. There are documented cases of severe reactions like encephalitis, Guillain-Barré Syndrome (GBS), and autoimmune hepatitis; all are lifelong injuries.

Herpes

Another hot dispute arises from the increase in Herpes Zoster outbreaks in children following Varicella vaccinations. If parents knew the contents of the Varicella shot, they'd think twice about inoculating their children with it.

The Varicella "vaccine" contains a live attenuated varicella-zoster "virus" (VZV), specifically the Oka strain, which is the same "virus" that causes both chickenpox (Varicella) and shingles (herpes zoster). It produces a distinctive dermatomal distribution of the shingles rash, which typically appears as a stripe on one side of the body or face, or spreads throughout the body.

Merck's Varicella patent reveals that the Varicella vaccine also contains the herpes simplex type 2 "virus vaccine," which is a standard component of all Varicella vaccines. Given that the Varicella vaccine contains a live (active) herpes pathogen, it would explain the outbreaks. If you inject a child with herpes, they may get herpes.

It's common these days for biotech firms to combine several vaccines into one; this way, it appears to parents as if their child is receiving fewer vaccines than they really are.

The Herpes simplex type 2 patent demonstrates how the vaccine is created in a lab using "Nitrous Acid Mutant Strain." The patent also states that it's a "viral disease," meaning it can aerosolize and infect others.

The Herpes simplex type 2 pathogen contains a lyophilized live Herpes virus." The pathogen is active and capable of infecting others. After inoculation, the Herpes pathogen aerosolizes through shedding or rather transmission, and it spreads to other people, potentially infecting them as well.

Nitrous acid is a highly toxic gas that "causes severe burns upon contact with skin or mucous membranes." The compound is highly toxic both by ingestion and inhalation.

Due to its corrosive nature and ability to react immediately with tissues, nitrous acid causes adverse effects primarily at the site of contact, including skin burns and irritation of the respiratory tract. According to the UK.Gov website, nitric acid also causes blisters, hours or days after exposure.

Now let's recap. Nitrous acid is a corrosive, aerosolized gas that causes skin burns and blisters hours or days after exposure.

Interesting. Now, why would a corrosive be in a vaccine?

My parents didn't vaccinate me in early childhood. However, when I was 10 years old, a medical doctor scared my mother into giving me a vaccine booster. Incidentally, days after the booster, I came down with a severe case of chickenpox. Coincidence?

After reading the Varicella patent, I have to wonder if there's a correlation between childhood vaccines and chickenpox. Are pharmaceutical companies giving children illnesses like chickenpox and herpes by subcutaneously injecting them with the very disease they profess to cure?

Let's investigate further.

Aborted Fetal Tissue

The biotech industry's Varicella inoculations use cell cultures from aborted baby fetuses. Human diploid cell strains (HDCSs) are cell lines derived from human fetal tissue, which are a preferred substrate for the production of human viral vaccines.

See the following NIH study on the human diploid fibroblast-like cell line using the lung tissue of a female fetus. The tissue has to be harvested from the fetus while it's still alive or immediately after death for tissue viability, which brings into question morality and ethics.

Below is a screenshot from Merck's Varicella vaccine patent.

Genetic Modifications, Chimeras, Graphene Oxide, and Cloning

Varicella contains an "open reading frame 68 (ORF68) which is a 623-amino acid type transmembrane protein." These are genetically modified recombinant proteins that encode artificial sequences into the human genome of target cells. These proteins are patented chemical drugs, owned by pharmaceutical companies. They encode target cells in your body and cause those cells to produce a chemical drug called "virions" on the surface of the target cells, which is a toxic spike protein.

Varicella contains mRNA, "lipid nanoparticle-encapsulated nucleoside-modified mRNA (mRNA-LNP) platform." In other words, they're using graphene oxide nanotechnology and calling it a "vaccine," as the NIH explains.

Here's a screenshot of Moderna's Varicella vaccine, which explicitly states that it uses a "plasmid DNA template."

A lyophilized live (active) Herpes "virus" was issued to Moderna, Inc. in 2023 for their Varicella vaccine, which contains a Herpes simplex virus (HSV) mRNA-1468 using a glycoprotein E (gE) antigen. It includes West Nile, dengue, and other flaviviruses. The glycoprotein E (gE) 's role is to evade the immune system, delete genetic codes in humans, and encode an artificial spike protein.

According to patents, Filovirus is a chimeric live, infectious, genetically modified yellow fever "virus". The invention is called CHIMERIVAX™-JE, made by Sanofi Pasteur. Chimerivax is produced in diploid fetal rhesus (monkey) lung (FRhL) cells from a chimeric (cross-species) monkey. This genetic material is derived from a full-length cDNA clone of YF 17D.

This chimeric clone is a synthetic chemical made to mimic the yellow fever "virus" plague. The clone is not a genuine pathogen that children would encounter in the wild; it's an artificial synthetic that you would never experience unless it were introduced into a population via inoculations.

In addition to these horrors, the RNA clone is blended with E. coli strains.

I previously documented in 2021 that cDNA (complementary DNA) is used to modify humans genetically for patent eligibility and slave ownership.

The varicella-zoster virus (VZV) ORF68 encodes glycoprotein E (gE), a critical component for “viral replication and spread.”

The term "ORF68" in humans typically refers to the gene C1orf68, which encodes skin-specific protein 32 at position 1q21.3, spanning 949 base pairs and containing a single exon without introns. It encodes a protein known as skin-specific protein 32, located on the open reading frame 68 of chromosome 1.

The C1orf68 gene encodes a skin-specific protein known as skin-specific protein 32 (XP32 or LEP7), which is highly enriched in the epidermis and plays a significant role in epidermal differentiation and the formation of the cornified envelope, a key component of the skin's barrier function. It contributes to maintaining the integrity of the cutaneous barrier.

The Varicella glycoprotein E (gE) encodes a 623-amino-acid type I membrane protein encoded by open reading frame 68 (ORF68). The NIH shows that ORE68 of skin cells and T-cells are the target, and "protein coding" is used to genetically modify them to alter their expression, "which is necessary for their life cycle in the human host."

ORF68 envelope glycoprotein E [ Human alphaherpesvirus 3 (Varicella-zoster virus) uses a gE–IE63 fusion protein, which is a recombinant chimeric protein from Chinese hamster ovary cells.

Varicella and Covid-19 Vaccines

The Varicella vaccine uses the same technology as the manufacturers of COVID-19 vaccines. The same mRNA nanotechnology being used in COVID-19 vaccines to "treat" SARS-CoV-2 is also the same technology in the Varicella vaccine. This explains why so many Covid-19 vaccinated persons got shingles!

Infertility

As I explained previously, the Varicella vaccine contains the herpes virus. A key component of the Varicella vaccine is the recombinant subunit herpes zoster vaccine Shingrix®. Interestingly, Shingrix was used to target the ovaries in Chinese hamsters during animal trials. Now, why would the Varicella vaccine be targeting the ovaries?

Wikipedia explains that Chinese hamster ovary (CHO) cells, an immortalized cell line, are the "most commonly used mammalian hosts for industrial production of recombinant protein therapeutics."

The website CHOgenome.org offers CHO mRNA cell lines for sale, specifically the CHO-K1 line, which is suitable for use in DNA microarray or RNA sequencing experiments. I know this is technical language, but please stay with me, as this is very important and I'm about to make it understandable.

CHO-K1 is a genetic tag.

Genetic tags, also known as markers, are used in CRISPR technology to direct the tech to cell groups of choice for genetic modification. Cell groups are always attracted to and find their way to their own cell group. This way, if you use ovarian cells from a hamster and attach them to the surface of nanotech as a genetic marker (tag) and inject them into a child (under the guise of a "vaccine"), the markers will drive the nanotech straight to the ovaries of the human child.

In essence, the Herpes invention within the Varicella vaccine is targeting the ovaries of female children, because governments and pharmaceutical companies know that our children deserve the best.

Genetic knockouts (deletions) and mutations in a child's ovaries will make the child less fertile or even sterilize the child.

In a 2009 study entitled, Gene knockouts that affect male fertility: novel targets for contraception, vaccines are explored for contraception. One hundred sixty-four genes were identified, and deleting them demonstrated an effect on fertility in male mice.

In 2010, a total of 150 genes were identified in female mice that, when gene knockout technology was used, had a contraceptive effect on female reproductive biology.

The Genscript website also offers CHO (Chinese hamster ovary) cells for mass sterilization.

Autoimmune Thrombocytopenia

In addition to targeting reproduction in our children, the Varicella inoculation also disables the immune system. One particular NIH Varicella vaccine study explains that the "gE antigen is highly immunogenic and elicits strong virus-specific CD4+ T cell and antibody B cell responses."

B cells are lymphocytes, or white blood cells, a key component of our innate immune system. CD4+ T cells, also known as killer cells, are another vital component of our innate immune system. Targeting and deleting genetic codes in these cells is a slow and painful death sentence that is rarely traced back to vaccines.

The Zostavax vaccine, made by Merck, and the Shingrix vaccine, made by GlaxoSmithKline Biologicals, are used together in the Varicella vaccine. An NIH study shows these two "vaccines," when tested together, are targeting T-cells and B cells to "evoke an immune response." If you put any poison whatsoever into the human body, it will evoke an immune response. Let's take a closer look at what's happening here.

The Zostavax patent contains poly(ethylene glycol) to enhance blood-brain barrier permeability. Zoztavax contains a TH-1 adjuvant patent comprising QS21, 3D-MPL, and liposomes, used to "evoke an immune response."

The TH-1 adjuvant patent explicitly states that this invention is targeting the induction of cytotoxic T cells through a "cytosolic DNA-sensing pathway that drives activation of type I interferons and other inflammatory cytokines." Our cells respond to a cytokine when they are poisoned.

QS21 and 3D-MPL are Saponins derived from the bark of the South American tree Quillaja Saponaria Molina. The Quillaja Saponaria tree and its extracts exhibit significant toxicity, particularly when ingested. It can cause liver damage, gastric pain, diarrhea, hemolysis, respiratory failure, convulsions, hemorrhaging, coma, and death.

The Saponin adjuvant patent, developed by Cambridge Biotech Corp, details how Quillaja saponaria extract is blended with acetic acid to produce Saponin. Acetic acid is highly corrosive and can cause severe health effects through inhalation, skin contact, eye contact, and ingestion. The acute toxicity is primarily due to its corrosive action and dehydration of tissues upon contact.

I don't see any logical reason for corrosives to be injected into children, unless you wish to poison them.

One study in particular shows that the Varicella vaccine can induce autoimmune thrombocytopenia.

But the horror doesn't stop here. Other poisonous adjuvants within Zoztavax would take another article to cover, so I'll go directly to the most shocking revelation.

Parasites

The Zostavax patent contains SEQ ID NO: 1. These are genetically modified parasites.

The “recombinant DNA vector” used in Varicella is the SEQ ID NO: 1, a patent owned by Bill and Melinda Gates through the Pirbright Institute, which contains the most deadly parasite vectors that carry the messenger RNA (mRNA) used to transfect (genetically modify) the human genome. Dr. Robert Young and I broke the news about parasites being the vectors or carriers of mRNA back in 2022.

Moderna’s new and improved Varicella jab for children includes the Pirbright Institute (Bill and Melinda Gates) SEQ ID NO: 1.

Biotech pharmaceutical companies (vaccines), the Government's wing DARPA (CRISPR), and Bill Gates (mRNA parasite vectors) are injecting our children with deadly material that makes them weaker genetically. These “vaccines” are targeting our children's fertility and deleting genetic codes to weaken their immune system, induce diseases, make them more susceptible to infections, reduce their quality of life and vitality, while shortening their life span.

This terrorism is without the Informed Consent of parents, under the guise of protecting their children from disease. Medical doctors are committing war crimes, governments are weakening our children, and pharmaceutical companies are profiting.

The Fraudulent Racket

Moderna's Varicella vaccine patent explains that the Varicella zoster vaccine (VZV) is included in the measles, mumps, and rubella vaccines (MMR) and is now present in higher amounts in the MMRV.

Moderna's Varicella vaccine patent explains that the Varicella zoster vaccine (VZV) is included in the measles, mumps, and rubella vaccine (MMR) and is now present in higher amounts in the MMRV vaccine.

The MMR vaccine is administered twice in the childhood schedule, first at between 12 and 15 months of age and again at 4 and 6 years. The Moderna patent admits that the Varicella vaccine will give your child chickenpox, shingles, herpes, and latent neural ganglia. It will be dormant and later activated, presenting symptoms of the herpes zoster. In essence, Pharma is giving your healthy babies these diseases, which are not natural.

Another NIH study reveals that the glycoprotein E (gE) of varicella zoster virus (VZV), encoded by ORF68, is the most abundant viral glycoprotein. Of course, our kids deserve the best!

Technically, Moderna's Varicella is a bioweapon, not a "vaccine." Varicella is a Gain-And-Loss-Of-Function technology. Gain-of-function refers to the process of genetically modifying biological organisms to enhance their toxicity. Loss-of-function is a gene deletion technology using DARPA's CRISPR.

The Moderna Varicella patent also states that it directly injects genetically engineered DNA (e.g., naked plasmid DNA) into human cells, producing an antigen. In other words, this is a "spike protein" being encoded into the genome of target cell groups. The genetic modifications cause the target cells to replicate with new, artificial genetic sequences, which then shed or transmit to others, whether they like it or not. And this is how shingles and chickenpox are infectious to others.

The Herpes zoster pathogen contained within the Varicella vaccine induces a slew of other life-long injuries, including myocarditis, thrombocytopenia, stroke, myelitis, arthritis, herpes, and more.

Last night I was in Safeway briefly to buy something. I heard an advertisement on the radio for the Shingrix vaccines, as a "treatment" for shingles. They said it "doesn't help everybody" and continued stating that shingles is dangerous because it "can cause Guillain-Barré" syndrome. The ad used fear to persuade people to take the perilous gene-altering jab, which they don't need, and used predictive programming to normalize the severe side effects it causes, blaming them on their symptoms.

Here is the racket. Pharma induces disease through childhood inoculations, then provides a "treatment" that further destroys your health.

If you develop shingles, it may be due to a parasitic infection or a viral shedding, and it definitely means you need to detoxify and boost your immune system.

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