This Is Accelerating': Suddenly, People in Their 30s and 40s Are Starting to Have Serious Health Issues
By Dr. Ariyana Love
The transhumanist dystopian nightmare we find ourselves in is taking a new turn with the shocking discovery of Hydra Vulgaris and PARASITES in the so-called Covid-19 âvaccinesâ.
Dr. Carrie Madej revealed her Hydra findings on the Stew Peterâs Show on September 29th, 2021, followed by Dr. Zandre Bothaâs 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 sheâs never seen before in her 15 years as a blood doctor.
About 10 days later, âThat Thingâ (Hydra Vulgaris) was also identified in Pfizer vials by Dr. Franc Zalewski. He took the science to a new 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 Hydraâs are being genetically modified before theyâre injected into humans. The good doctor also identified parasites in the vials.
Dr. Jane Ruby, a pharmaceutical researcher, gave vital commentary on Stew Peterâs Show about Dr. Zalewskiâs findings, emphasizing that the dormant Hydra âeggsâ 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. Youngâs findings.
Investigative Journalist Ramola D. provided us with further informationabout the parasites discovered by Dr. Young and did an expose in October.
Back in July, La Quinta Columna studied four âvaccinesâ; Pfizer, Moderna, AstraZeneca, and Johnson & Johnson, and found toxic nano metallic particulates, particularly nanographene oxide, in significant amounts, as well as lipid nanoparticles and the parasite Trypanosoma cruzii, in the Pfizer-BioNTech serum.
Pfizer whistleblower Karen Kingston appeared on Stew Peterâs Show in July and walked us through a presentationon 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 itâs 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 âGraphene Oxide The Vector For Covid-19 Democideâ. 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 itâs clear there are 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 Peterâs Show. Kingston explains that the vaxxines are a âgateway to an obedienceplatform and potentially an executionplatform if you are not obedient to your scoreâ.
Informed Consent has been waived and therefore people didnât know theyâre being injected with smart devices and bioweapons. The patents also reveal that it was already known by Pfizer that the vaxxed would become âsuper spreadersâ and transmit deadly pathogens to healthy individuals.
Thereâs an AI component to these vaxxines Kingston explains, âtheyâre committed to replacing the American people with Artificial Intelligenceâ. She continues disclosing that âHong Kong is ready to replace the American people with robots right nowâ.
Due to the fact that patent filings do not reveal the components to Biotechâs vaxxine ingredients, I began researching scientific peer-reviewed studies involving Hydra Vulgaris and parasites to see if I could identify why theyâre being injected into humans.
GAIN-OF-FUNCTION
Everything Iâm 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 Vulgaristransgenesis 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. Hydraâs 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 Hydraâs and parasites are all part of an âoperating systemâ which is bypassing the human immune system. You can read more about Modernaâs âoperating systemâ from their own website, here.
Graphene Oxide sheets are used to slice open the membrane of your cells so that programmable Nanorobots 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 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 26â28, in 2017, in Beijing, China where the forum showcased the applications of self-assembled DNA nanostructures.
CHIMERIC SPIKE PROTEIN
The âspike proteinâ in the Covid-19 vaxxines that everyone is talking about is called a Lentivirus. The Lentivirus contains a combination of HIV types 1-3, SRV-1/AIDS, MERS, and 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 âgenus of retroviruses that cause chronic and deadly diseases characterized by long incubation periods, in humansâ. It enables long-term transgene expression. The best-known Lentivirus is the human immunodeficiency pathogen, which causes AIDS. This is why weâre seeing an 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 that permanently changes the genome of that cell. Once inside the host cellâs 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 2.0 GENOME ASSEMBLY
Hydraâs are used in cross-speciesgenomics. Theyâre being genetically modified in a lab at the University of Kiel 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 were developed to learn the neurobiological functions of humans and for in vivo tracing of cells. Transgenic Hydra allows in vivo tracking of individual stem cells during morphogenesis (tissue and cell growth).
Transgenic Hydra lines are generated by embryo microinjection with plasmid DNA from self-replicating DNA found inbacteria. 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 âcloningâ processcalled transfection. A new generation of transgenic Hydra polyps continues 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 rewireand control the ancestral circuitry of human beings.
BLAST Sequence technology is being used to create new DNA sequences and find 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 Hydraâs 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-Cas9technology and electroporation.
Electrodes attached to gold programmable nanorobots transfect human cells, silencing your innate God-given genetic sequences and coding 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 thechimeric pathogen you were injected with. The same chimeric pathogen was funded by bioterrorist Anthony Fauci and developed in Wuhan, China.
One of the deadly bacteria being chimerically enhanced to transfect Hydraâs for implantation into humans is E. coli, which causes about 36% of the infections in humans.
PARASITES
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 Projectdeveloped 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. Itâs important to be aware that from the P. falciparum they designed a Chloroquine-resistant transgenic parasite strain called Dd2.
LUCIFERASE
Hydra polyps are also being coded with the overexpressed chimeric proteincalled Luciferase, which is a Green Florescent Protein derived from the firefly. Transgenic Hydra also carries 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 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. Thetransplanting of Hydraâs into humans is called Homoplastic transplantation using induced Hydranth as âimplantsâ.
Epithelial cells are stem cell lineages responsible for cell signaling. Transgenic Hydraâs reporter genes are cell-signaling with each other inside humans, much like neurons in a neural network. Transgenic Hydraâs 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 (HySp5â2992:Luc); aka transfection.
Transgenic Hydra 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 Hydraâs, parasites, and newly hybridized humans.
In fact, Biotechâs chimeric operating system establishes a new neural networkin 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 âhear your brain whisperâ.
A team of scientists from UC Davis and Rice University was boasting back in July about manipulating the nervous system of Hydra Vulgaris and humans to âbuild a new brain from the bottom upâ, in order to control neural pathways and human behavior. This technology was developed over the last decade through the Human Brain Project.
The European Unionâs 1.5 billion euro Graphene Flagship project developed graphene-based implants for âfuture brain-computer interfacesâ. I have to wonder if the âimplantsâ theyâre referring to contain transgenic Hydraâs?
Graphene implants can record electrical activity in the brain at extremely low frequencies and over large areas, âunlocking the wealth of information found below 0.1 Hzâ.
A Russian initiative called 2045 wants to use neural interfaces for an âimprovement of man himself â because mankind is âstanding at the edge of a total loss of the conceptual guidelines necessary for further evolutionâ. This demonstrates the anti-human mindset of eugenicists who want to clone the entire human race.
The fluorescent (Luciferase) Hydraâs were also tested with externally applied electrical fields to see how much voltage they could endure, to âfacilitate the future use of electric fields as an experimental means to redistribute intracellular constituents in developing tissuesâ. I presume this was to test Hydraâs ability to survive 5G frequency?
THE OPERATING SYSTEM
Hydraâs and parasites also serve as a reporter system. Luciferase exhibits bright green fluorescence when exposed to light in the blue to the ultraviolet range, enabling the vaxxed to be traced externally. Genes of interest can be turned off occasionally or turned on at will by your patent holders through whatâs called transregulation.
This means youâre not only externally traced 24/7 but youâll also be externallycontrolled. Your patent holders will be able to upregulate and downregulate your genetic codes through an external database, through the Eukaryotic Genome Annotation Pipeline for transgenic humans.
Did you think the Starlink satellite networkâs âPrecision Tracking Space Systemâ had something to do with defense? Donât worry, youâll be âhappyâ owning nothing so long as they get your dopamine levels worked out.
ADDGene is selling a variety of CRISPR parasites to be used as gene vectors for human transfection. These are not âvaccinesâ at all but a WEAPONS SYSTEM (my words) for the RAPID CLONING (their words) of humans, through gene knockout (silencing), artificial gene sequencing (coding) and to monitor transfectants inside of humans (tracing).
ProSplign is a worldwide protein-to-genome alignment tool enabling Human DNA to be easily synthesized from a single-stranded RNA template and catalyzed by an enzyme for reverse transcriptase.
ADDGene also offers a Lentiviral Envelope and Packaging Plasmids for transfecting humans using transgenic Hydra. They offer âNon-overlappingNEURAL NETWORKSâ (their words) using Hydra Vulgaris for building a new neural network in Hydraâs. This technology is being deployed in humans through the Coivd-19 Quackccine program now.
Dr. Carrie Madej also disclosed in her latest interview on Stew Peterâs Showthat the vaxxine operating system is building an artificial neural network in humans.
ADDGene offers a Tetracycline off system for on/off gene expression, âfusing tetR with the C-terminal domain of VP16 (virion protein 16), an essential transcriptional activation domain fromHSV (herpes simplex virus) which is being used for âreduced gene expressionâ in humans. This uses the chimeric E. coli bacteria and Lentivirus.
The Hydra genome assembly offers a Nano DNA kit called Illumina. Illumina Inc figured out how to reduce the cost of sequencing a human genome down from $1 million to $1,000 USD, back in 2007.
After Luciferase is infused and coded for targeted genes via a computer, itâs then mapped onto the Human through the public Galaxy server to perform âdifferential expression analysisâ. Proteins can be targeted, upregulated, and downregulated.
Then thereâs Vector Biolabs whose selling Adenovirusâ for human sp5 shRNA silencing. A Knockout vector system (adenovirus) for knocking down the expression of particular genes (gene silencing), is being marketed online and sold by Vector Builder. You can create artificial genome sequences and merge genomes of different species.
You can preorder DNA sequences for humans on HydraAtlas website.
The Genome Data Viewer (GDV) will help you select genome assemblies (DNA sequences) for humans from primarily finished human clones, that were sequenced as part of the Human Genome Project.
VIGENE offers multiple shRNA cloning options for your gene silencing experiments. Theyâre packaging transfer Plasmids, Adenovirusâ (AAV) and Lentivirusâ and they guarantee at least a 70% knockdown of your gene of interest. They have a catalog of over 27,000 shRNA plasmid sets targeting the human genome.
This table lists common Lentiviral envelope and packaging plasmids that can be used with 2nd and 3rd generation lentivirus technologies.
ADDGeneâs lentiviral genome is delivered to a target cell upon infection using CRISPR gRNA. They explain how the Lentiviral genome encodes genetic material that the âresearcherâ (or patent holders and Big Pharma) wants to be delivered to specific target cells. The genome is encoded by plasmids called âtransfer plasmids,â which can be modified to encode a wide range of gene products.
ADDGene admits their DNA-targeting enzymes very often will delete, insert or otherwise alter the targeted RNA or DNA, so donât let the fake media fool you.
Lentiviral Plasmids can be ordered through ADDGene here.
BEHAVIOR CONTROL
Vector Biolabs offers an Adenovirus (AAV) expressing shRNA for the knockout (gene silencing) of Human SP5. When developing this technology during the animal trials, social recognition, spatial learning, and memory were impaired after 4 weeks.
In an animal study using reverse transcriptase-polymerase chain reaction (RT-PCR) with an Adenovirus vector and drugs, scientists were able to induce Huntingtonâs Disease by targeting the Corpus striatum of the brain which resulted in 100 fold neurodegeneration and motor behavioral impairment.
REPRODUCTION & FERTILITY
The transgenic Hydraâs are used to induce gene silencing predominantly targeting embryonic cells in the testes of men and the ovaries of women and also nerve cells. This is why weâre seeing neurological degeneration (PRION) after inoculation. It also explains why 82% of expectant mothers who take the âjabâ are having spontaneous abortions.
Microinjection of foreign DNA into the pro-nucleus of single-cell embryos of fertilized mice to control the genetic expression of future generations has been perfected, since 2008.
Proteins control gene expression. Transgenic Hydra is instrumental in encoding the human SP5 (shRNAsilencing AAV) which is a gene on chromosome 2q31.1 that encodes a protein that binds to the GC-box promoter elements, thought to play a role in coordinating the intricate changes in transcription which occur in the developing embryo.
Wnt-3 is a protein that in humans is encoded by the WNT3 gene. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis.
The point Iâm making here is that the operating system is DNA-binding, downregulation, and upregulating genes using the transgenic Hydraâs, targeting human embryos and embryonic cells, leading to developmental alterations from binding genes to the Wnt/ÎČ-catenin signaling pathway.
Do you understand what this means? Itâs not only the vaxxed who are being genetically modified, cloned, and hybridized, but SO ARE THEIR OFFSPRING! That is of course if youâre still able to reproduce at all after the jab! Most people will just be sterilized and their babies aborted. This is a human cloning experiment as well as extermination.
Microinjection of Retrovirus transgenes (Lentivirus & Luciferase) integrates randomly into the genome which poses enormous risks for the vaxxed as well as their hybrid offspring. This can create strange and unpredictable mutations of DNA by the addition of one or more base pairs. This is precisely why weâre seeing freaky mutations and why doctors are removing blood clots with Hydra-like tentacles from teenagers!
If you still arenât convinced, please listen to Dr. Peter McCullough explain this biotechnology and how the chimeric spike proteins are being coded into human cells, at the 78th Annual Meeting of Association of American Physicians and Surgeons, on October 2, 2021.
âIt is a deadly proteinâ explains Dr. McCullough. âIt is the first time in medicine that we are injecting vaccines and asking the human body to make a potentially lethal proteinâ .
While the Covid-19 serums appear on the surface to be only a clear liquid, under microscopy you can visibly see all the many components of the computer-interface operating system, which is a sophisticated biological weapons system for the cloning and extermination of the human race.
FINAL NOTE
If you would like more information on detox protocols and disrupting the blood coagulation cascade which leads to blood clots from the jab or for protocols that will protect you from the adverse effects of transmission, please contact me directly at: metanutrients@mailfence.com
No comments:
Post a Comment