Transgenic Hydra’s & Parasites A Biological Weapons System For Rapid Human Cloning

November 1, 2021 | By Dr. Ariyana Love | Photo Source

“The transhumanist dystopian nightmare we find ourselves in took a new turn with the shocking discovery of Hydra Vulgaris and PARASITES in the so called Covid-19 “vaccines”.

Dr. Carrie Madej revealed her Hydra findings on the Stew Peter’s Show September 29th 2021, followed by Dr. Zandre Botha’s stunning discovery of microscopic, self-assembling medical devices in the blood of her vaxxed patients. The red blood cells are dangerously deformed and coagulated, things she says she’s never seen before in her 15 years as a blood doctor.

About 10 days later, “That Thing” (Hydra Vulgaris) was also identified in Pfizer vials by Dr. Franc Zalewski. He took the science to a knew level and did a chemical analysis of the Hydra, exposing that the chemical compound of the creature contains aluminum, carbon and bromium. This means the Hydra’s are being genetically modified before they’re injected into humans. The good doctor also identified parasites in the vials.

Dr. Jane Ruby, a pharmaceutical researcher, gave vital commentary on Stew Peter’s Show about Dr. Zalewski’s findings, emphasizing that the dormant Hydra “eggs” become active, grow and multiply when exposed to Graphite tape and heat.

Earlier in August, parasites and other horrors were identified by Dr. Robert Young in four Covid-19 vials. Dr. Jane Ruby again joined Stew Peters to give crucial commentary on Dr. Young’s findings.

Investigative Journalist Ramola D. provided us with further information about the parasites discovered by Dr. Young and did an expose in October.

Back in July, La Quinta Columna studied four “vaccines”; Pfizer, Moderna, AstraZeneca, and Johnson & Johnson and found toxic nanometallic particulates, particularly nano graphene oxide, in significant amounts, as well as lipid nanoparticles and the parasite Trympanosoma cruzii, in the Pfizer-BioNTech serum.

Pfizer whistleblower Karen Kingston appeared on Stew Peter’s Show in July and walked us through a presentation on how Graphene Oxide is in all Covid-19 serums. Graphene Oxide was not listed in the patent filings and was deliberately concealed under a trade secrete because it’s known to be poisonous to humans.

As a result of these horrifying discoveries, I did my own research on Graphene Oxide Nanoparticles and Toxicity and wrote an article entitled “Graphene Oxide The Vector For Covid-19 Democide“. I reveal how humanity is being saturated with Graphene Oxide Nanoparticles in a myriad of ways.

I also wrote an article on protocols for detoxifying Graphene Oxide from your body, here.

The openly declared ingredients in Covid-19 serums should be enough to dissuade anybody from taking them. Now it’s clear there’s additional poisonous and other horrors not being disclosed to the public by the Biotech pharma industry.

Karen Kingston has backed up all these terrifying discoveries with the patent filings and receipts, on Stew Peter’s Show. Kingston explains that the vaxxines are a “gateway to an obedience platform and potentially an execution platform if you are not obedient to your score”.

Informed Consent has been waived and therefore people didn’t know they’re being injected with smart devices and bioweapons. The patents also reveal that it was alreadyknown by Pfizer that the vaxxed would become “super spreaders” and transmit deadly pathogens to healthy individuals.

There’s an AI component to these vaxxines Kingston explains, “they’re committed to replacing the American people with Artificial Intelligence”. She continues disclosing that “Hong Kong is ready to replace the American people with robots right now”.

Due to the fact that patent filings do not reveal the components to Biotech’s vaxxine ingredients, I began researching scientific peer reviewed studies involving Hydra Vulgaris and parasites to see if I could identify why they’re being injected into humans.


Everything I’m writing here is based on evidence from open source, peer reviewed literature of scientific breakthroughs and technological developments that extend through the past decades and are linked in this article. As sci-fi thrilling as this information may sound, the technology has already been deployed and is being injected into the veins of our children as we speak. You can read the studies for yourself, as I have done.

DNA hybridization began in 1980 with Nadrian C. Seeman who started constructing self-assembled nanostructures. Hydra Vulgaris transgenesis technology was developed over the last 30 years. This is the process of transferring genes and organisms from one species to another which creates a new cloned species.

The Human Genome Project began in the year 2,000. Hydra’s are used in the human genome assembly for gene silencing of humans. Messenger RNA (mRNA), SPIONS (Super Paramagnetic Iron Oxide Nanoparticles), DNA coated lipid-nanoparticles containing drugs and chemicals, transgenic Hydra’s and parasites are all part of an “operating system” which is bypassing the human immune system. You can read more about Moderna’s “operating system” from their own website, here.

Graphene Oxide sheets are used to slice open the membrane of your cells so that programmable Nano robots can reach the cell nuclei to turn off undesired genes (gene silencing) and code artificial gene sequences. This process is called biohacking.

Graphene Oxide sheets are able to slice open every cell membrane of the human body within 15 minutes after inoculation, according to Dr. Robert Martin.

DARPA partly funded the development of protein-to-genomic sequence alignments for cross-species genomics. Gain-Of-Function and Loss-Of-Function studies using transgenic Hydra’s were funded by Fauci and the NIH and developed at the Wuhan Institute in China and in universities in the U.S. and China. Their scientific findings were published in 2013.

The Sixth International Workshop on DNA Nanotechnology was held August 26–28, in 2017, in Beijing, China where the forum showcased the applications of self-assembled DNA nanostructures.


The “spike protein” in the Covid-19 vaxxines that everyone is talking about is called aLentivirus. The Lentivirus contains a combination of HIV types 1-3, SRV-1/AIDS, MERSand SARS. These are the most deadly Gain-Of-Function bioweapons ever developed, thanks to mass murdering Fauci.

A Stanford study reveals that the Lentivirus is a “genus of retroviruses that cause chronic and deadly diseases characterized by long incubation periods, in humans”. It enables long term transgene expression. The best known Lentivirus is the human immunodeficiency pathogen, which causes AIDS. This is why we’re seeing autoimmune and neurodegenerative decline after Covid-19 inoculation. This is an induced condition known as PRION.

The mRNA from the Lentivirus chimeric cocktail is inserted into the DNA of human cells through an invasive procedure which permanently changes the genome of that cell. Once inside the host cell’s cytoplasm, lipid coated nanobots take the reverse transcriptase enzyme in the Lentivirus to produce DNA from the mRNA genome, the reverse of the usual pattern, thus retro.


Hydra’s are used in cross species genomics. They’re being genetically modified in a lab at the University of Kiev to produce transgenic clonal Hydra lines. Since 2006, thousands of embryos have been microinjected and nearly 200 transgenic lines have been established in the Hydra Transgenic Facility.

Morphogenesis and stem-cell control using the Hydras was developed to learn the neurobiological functions of humans and for in vivo tracing of cells. Transgenic Hydra’sallow in vivo tracking of individual stem cells during morphogenesis (tissue and cell growth).

Transgenic Hydra lines are generated by embryo microinjection with a plasmid DNA from a self-replicating DNA found in bacteria. This is a permanent transmissible change of genetic material (DNA) resulting in the decreased production of a protein. The merging of the two species is a “cloning” process called transfection. A new generation of transgenic Hydra polyps continue reproducing the chimeric genetic expression in their offspring.

These GMO Hydra polyps are now genetically coded vectors, carrying a variety of programmed synthetic genomic sequences and mRNA (messenger RNA) for the purpose of transfecting humans. Once inside the human body, these transgenic Hydra polyps serve to rewire and control the ancestral circuitry of human beings.

BLAST Sequence technology is being used to create new DNA sequences and finds similar genetic sequences between species, performing alignment functions for same-species and cross-species genetic splicing for the purpose of transcription.

Proteins regulate gene expression. This technology targets the cell organelles of the nuclei which store genetic information; mitochondria, which produce chemical energy; and ribosomes, which assemble proteins, using mRNA to make mitochondrial sequences.

A 2017 Gain-Of-Function research project from Germany, demonstrates how RNA extraction and quantitative reverse transcription polymerase chain reaction or reverse genetics is used to knockout and knockdown genes using Hydra’s and CRISPR/Cas9.

The genetically modified Hydra lines in the Covid-19 operating system is first coded with chimeric gene sequences (Lentivirus) which is then being coded into human cells using CRISPR-Cas9 technology and electroporation.

Electrodes attached to gold programmable nano robots transfect human cells, silencing your innate God-given genetic sequences and code your cells to reproduce the synthetic genetic sequence of the chimeric spike protein (Lentivirus), indefinitely. More simply stated, your cells will continue to replicate themselves over and over again with the new genetic sequence of the chimeric pathogen you were injected with. The same chimeric pathogen that was funded by bioterrorist Anthony Fauci and developed in Wuhan, China.

One of the deadly bacteria being chimerically enhanced to transfect Hydra’s for implantation into humans is E. coli, which causes about 36% of the infections in humans.


Parasites are also transfected with bacteria and used as transfection vectors for DNA binding and genetic sequencing in humans. Parasites can evade drugs, escape the immune system and regulate genes.

The human Malaria Genome Project developed at Stanford University, used CRISPR technology and bacterial plasmids which can replicate rapidly inside parasites. They transfected bacterial plasmids into parasites, disrupting a series of gene encoding molecules. In that study, scientists transfected Malaria parasites with Luciferase to use it for gene targeting and transgene expression in humans.

T. gondii and P. falciparum and other parasites were also used in transfection studies. It’s important to be aware that from the P. falciparum they designed a Chloroquine-resistanttransgenic parasite strain called Dd2.


Hydra polyps are also being coded with the overexpressed chimeric protein called Luciferase, which is a Green Florescent Protein derived from firefly’s. Transgenic Hydra’s also carry the Luciferase RNA trigger to code your cells with and silence genes in human cells.

Holstein lab investigated the repressing activity of HySp5 on the HyWnt3 promoter, performing Luciferase reporter assays in human HEK293T cells for DNA-binding and transplanting Hydra into humans by invading human tissues.

The transgenic Hydra’s and parasites replicate and merge with humans during transfection. They are integrated with the transgenes (Luciferase and Lentivirus) into one of the epithelial cell lineages and assimilated into the human host. The transplanting of Hydra’s into humans is called Homoplastic transplantation using induced Hydranth as “implants”.

Epithelial cells are stem cell lineages responsible for cell signaling. Transgenic Hydra’s reporter genes are cell signaling with each other inside humans, much like neurons in a neural network. Transgenic Hydra’s cell signaling becomes synthesized with human cell signaling in a process called catenin signaling, which is induced by mutations of genes in humans through upregulation (cell response) to the plasmids expressing activators in the Hydra (HySp5–2992:Luc); aka transfection.

Transgenic Hydra’s and parasites induce humans to generate a new electrochemical signal by organizing enzymes spatially to create a programmable redox enzymatic cascade pathway, changing the predictable generation of electrochemical signals in humans. The newly established synthetic gene sequences are now shared between the transgenic Hydra’s, parasites and newly hybridized humans.

In fact, Biotech’s chimeric operating system establishes a new neural network in humans and an artificial brain by re-directing endogenous neural stem cells. Brain implants can erase memories and implant new, artificial memories while Graphene Oxide can “hear your brain whisper”.

A team of scientists from UC Davis and Rice University were boasting back in July about manipulating the nervous system of Hydra vulgaris and humans to “build a new brain from the bottom up”, in order to control neural pathways and human behavior. This technology was developed over the last decade through the Human Brain Project.

The European Union’s 1.5 billion euro Graphene Flagship project developed graphene-based implants for “future brain-computer interfaces”. I have to wonder if the “implants” they’re referring to contain transgenic Hydra’s?

Graphene implants can record electrical activity in the brain at extremely low frequencies and over large areas, “unlocking the wealth of information found below 0.1 Hz”.

A Russian initiative called 2045, wants to use neural interfaces for an “improvement of man himself ” because mankind is “standing at the edge of a total loss of the conceptual guidelines necessary for further evolution”. This demonstrates the anti-human mindset of eugenicist’s who want to clone the entire human race.

The fluorescent (Luciferase) Hydra’s were also tested with externally applied electrical fields to see how much voltage they could endure, to “facilitate the future use of electric fields as an experimental means to redistribute intracellular constituents in developing tissues”. I presume this was to test Hydra’s ability to survive 5G frequency?”

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