The Elegant Bioweapon - A Love Story
From a Belgian King's Nazi Vaccine to Encapsulated Reverse Transcribing Gene Therapies
So many layers to this onion. Find presented below an outline of the myriad of intricate weapons (bio, radiation, toxin, viral, psyop) being used upon innocent humans, followed by some detailed reading. Tried to keep this as “high-school science” as possible, but questions are welcomed and research can be provided ad nauseum.
Outline of elegant weaponry being utilized:
LNP - Lipid Nanoparticle (future post) - allows spike to go to brain and everywhere. Also cytotoxic on its own
Arbutus Pharmaceuticals - Trudeau Foundation
5G causing SARS and also cellular immunity reduction
perfect environment for spike protein to adhere in lungs
Several systems disrupted (eg. immunoglobulin A & G reduction)
ACE2 present in lungs during any SARs event
eg. 300 Botswana elephants dropped dead when Huawei donated 5G was turned on at University of Botswana of ‘mysterious bacteria’
EMF causes oxidative cellular stress and also a reduction of antioxidant defenses
*Spike Protein known subunits*
Glycoprotein 120
Multifunction bioweapon by itself
attaches to sugars on cells (glycoRNA),
folds itself specifically for RNA transfer,
a prion in itself (misfolding protein) that forces healthy cells to misfold as well
disrupts multiple important cellular functions and communication
RBD (Receptor Binding Domain/Site)
Inserted subunit specifically designed to target ACE2 receptors in already-inflamed-from-5G-lung-cells where ACE2 is most prevalent
Perfect viral/vaccine RNA entry point into cells
Main area that new variants WILL occur - as people get spike protein sickness in other areas, other ACE receptors or Immunoglobulin subsystems (human antibodies) become infected and begin misfolding protein - thus created variations and mutations.
Our sick bodies are currently creating the next world ending virus and ‘they’ KNOW IT
1.) LNP encapsulated mRNA goes somewhere in body where inflammation is greatest
2.) mRNA attaches to cell there via low valency-bond required glycoprotein 120
3.) local infected cell starts producing spike protein and the protein misfolding begins to match the receptors of the localized cells (brain for instance)
4.) new variant virus created now automatically becomes central nervous system attacking variant (Herpes + AIDs = encephalitis)
Furin Cleavage Site
Where AIDS becomes cancer
future trojan horse for reactivation of previously immune generational disease - the end-end game
mRNA
Software building its own hardware
computer created single-stranded RNA instructions for cells to build what, exactly?
miRNA and siRNA (microRNA - short strands & silencerRNA - gene silencers)
Reverse transcription into our DNA?
What species will we become - CRISPR(future post) & J. Craig Venter
Transposon mutagenesis
Military/Security State Actors driving vaccination
War of our brains - DREADDs - Designer activated cells - Dr. Charles Morgan
5G Full-circle - Neural Net Built and Electromagnetically controlled brain cavitation
‘Advanced Scientific Integrated Technologies’ a whole host of capabilities under a broad rubric of brain science - Dr. James Giordano
The beginning… WWII Ends
Birth of the king-made viral Glycoprotein
After the staunch nazi supporter and traitor to his own country (joke is on you, all monarchs support fascism) King Leopold III of Belgium went into exile in Austria (1944), via orders from Heinrich Himmler himself, he then ‘transferred’ to ‘neutral’ Switzerland until 1950. Once the elderly and academics were cleansed from Belgium, Leopold III ran a totally fair and authentic referendum where the rich-Catholic sub-monarchs (installed political puppets like today) moved right over and the king returned to power on March 12, 1950. “Let them eat bioweapon cake.” - king Leo III - regarding HIS family’s territory in the Belgium Congo (Zaire).
Looking right back to his nazi roots, king Leopold III engaged IG Farben to begin creating genocidal agents and toxins (after all, he used his people’s taxes and dead relative’s gold to build the company). For those that do not know IG Farben, well you don’t know Jack, because IG Farben is now Blackrock again and they fulfilled their task of creating a fourth reich that will reign a thousand years. The board of directors of IG Farben referred to themselves as ‘the council of gods’ and ran a security force of 1,200 spies around the world (which became the nazi ss, the US OSS and eventually the CIA). Oh, and they (BASF, Bayer/Monsanto, AGFA/Gevaert, Hoechst/Sanofi, Cassella, Chemische Fabrik-Elektron and Chemische Fabrik vorm) also produced Zyklon B (nazi final solution), Sarin (nerve agent), Dioxin/Agent Orange, DDT, PCBs, Mustard Gas, glyphosate (Roundup - the REAL WORLD emergency going on) and dozens of other death chemicals such as the oral polio vaccine (OPV). The creator of this OPV bioweapon was Dr. Albert Sarin, Polish immigrant and murderer of brown children around the world. ‘Where did polio come from?’, is another entire post…
In 1959 the Belgian Congo began a forced campaign of oral polio vaccines (OPV) to children with a 1 in 750,000 chance that they “can mutate back to a more neurovirulent form”. Here is Anthony Fauci discussing the existence of AIDS in the early 70’s and the OPV/Zaire/Haiti connection to the creation of a new type of sub-virus with similar capabilities of polio to penetrate the human cell, but now coated with an enveloped glycoprotein (membrane protein). These glycoproteins are linked to oligosaccharides (simple sugars on cells) which allow the viral protein to participate directly or indirectly with cell-cell interactions through the RER (rough endoplasmic reticulum, the outside of the cell - grade 7 cellular science). “The RER is associated with many roles in protein synthesis, which also include post-translational modifications, folding, and sorting. Membrane-bound ribosomes (RNA and proteins) in the RER translate the mature mRNA transcript into amino acids that are attached to become polypeptides (many, short chained amino acids)”. Abnormalities in the RER are caused when proteins in the RER undergo slight modifications when their electric signals are cleaved (not enough micronutrients and substrate - zinc, magnesium… etc.) or undergo glycosylation (oligosaccharides added to produce a glycoprotein). This explains Walter Chestnut’s research below on why this is sugar driven.
Gleeful Glycoproteins and Glycoconjugate Glycans
What the… haha. Ok, here we go, wiki, any help? - “Glycoconjugates are the classification family for carbohydrates – referred to as glycans – which are covalently linked with chemical species such as proteins, peptides, lipids, and other compounds. Glycoconjugates are formed in processes termed glycosylation. Glycoconjugates are very important compounds in biology and consist of many different categories such as glycoproteins, glycopeptides, peptidoglycans, glycolipids, glycosides, and lipopolysaccharides. They are involved in cell–cell interactions, including cell–cell recognition; in cell–matrix interactions; in detoxification processes.”
So what???? Simplest answer: Sugar makes you sick. I said it. Without any sugars, there is no place for any of these glycoprotein envelopes to land and spew their junk RNA into our cells. A healthy and robust cell, with all the proper nutrients provided by nature - water, vitamins, nutrients that become microscopic proteins that our cells use as building blocks etc., will not allow AIDs or SARs or Polio or other man-made toxins to adhere and do their damage.
The latest discovery is that glycoRNAs are on the cell surface (sugar coated RNA molecules that attach to the cell) and aid viral glycoproteins to attach and adhere directly to human cells. These glycoRNA are capped with sialac acid which directly interact with Siglecs (a class of proteins that regulate immune cells). So to put it simply: simple sugars make it easier for glycoprotein encapsulated viruses to adhere and transcribe their RNA payload into our cells.
Glycoproteins - AIDS, VAIDS and The Spike Protein
Glycoprotein 120 is ‘found’ in HIV and the Spike Protein of covid-19. We have a vaccine-derived creation theory about glycoprotein 120, so how does it work?
Glycoprotein 120 is a prion (misfolded protein, see above figure) which has the ability to transmit their folded shapes onto normal variants of the same protein. Prions are classified in molecular biology as ‘intrinsically disordered proteins’ and thus participate in weak multivalent bonding (to glycoRNA for instance). So these spike proteins attach easier as cells are weakened through stresses such as mental (psychosomatic), environmental (EMF waves and toxins), biological (vaccines, glysophates and radioactive compounds), socioeconomic (high sugar diets and inflammation prone lifestyles), and so forth.
Catchup - Step 1 in the bioweapon process - make a viral envelope that attaches easier to weakened cells.
Step 2 - make these attached structure also exert a function on the cell. How?
Well, first you inflame and weaken the cells. The reason that AIDs went rampant through the gay, party-community had nothing to do with anything other than the weakening of their cells through their chemical-dependent, sleep-deprived, low-nutrient lifestyles. No different to the majority of obese humans living off of sugary (Food Guide - based) diets. Want to know who is mostly dying of covid? The obese. Sorry.
After weakening the cells, via inflammation, the sticky envelope attaches the virus and then begins to fold. Glycoprotein 120 (GP-120) is a prion that folds over and attaches to the cell in two points, thus creating a zero-electron transfer point. This is where GP-120 has completed it primary two objectives.
Receptor-Binding Domain (RBD or RBS - receptor binding site)
Once GP-120 has passed the baton, the next interesting piece of our elegant bioweapon is the receptor-binding domain (RBD) that was lab-created-inserted into the structure of the man-made spike protein. The RBD is how the virus interacts with the much touted ACE2 human cell receptors but is also the main area for viral escape mutations to occur. Variations between delta and omicron were found mainly in this site.
What is ACE2 - More than just a ‘telephone’ to the nucleus of cells
Scientists like to throw out terms to confuse you. Here is one: Angiotensin-converting enzyme 2 (ACE2). Easy, right? Let us break this down. Angiotensin - a peptide (in the Serpin family of proteins - see above - glycoRNA) hormone that has several important cellular functions; including control of vasoconstriction and an increase in blood pressure. It also acts as Na+/H+ exchanger to stimulate Na+ reabsorption and H+ excretion which is coupled to bicarbonate reabsorption (partly why sodium bicarbonate works against covid). Hence the big push to add NAC+, Niacin etc. to diets to combat pre-infection. Other functions of the ACE enzymes include Adipic (fat mass expansion - hence obesity-growing long covid), Cardiovascular direction of vasoconstrictors (hence the micro-constriction of blood vessels and capillaries etc), Prothrombotic adhesion and aggregation of platelets (Thrombocytopenia - leading to cardiac cell growth through protein ‘kinase c’ ie. Myocarditis & Pericarditis - Got Myocarditdits), acts on the adrenal cortex causing a release of aldosterone - causing kidneys to lose potassium and retain salt (hence why everyone is acting like a fucking idiot - like seawater poisoning), and on and on.
So to summarize: the lab-inserted RBD not only interacts with ACE2 but begins the process of disruption across multiple bodily systems required to live. Thus the immediate increase in a wide range of diseases and conditions. Elegant so far?
S1 and S2 Subunits of Spike Protein - Furin Cleavage Site is the Glue
As part of the process of the above glycoprotein 120, glycosylation (glycoconjugates are formed through glycosylation - see above) is stimulated through protein folding and this glycosylation also causes the next step in the bioweapon to kick off. Another lab-inserted smoking gun is a group of amino acids called the PRRA Furin Cleavage Site (patent here - check out the rest of Dennis Brown’s North Carolina bioweapons work). The Furin Cleavage site increases the infectivity to the cell itself. Furin is a protease (enzyme that catalyzes/speeds up the breakdown of proteins into smaller proteins - miRNA Dicer and DROSHA post) and is created when GP-160, GP-120 or GP-41 precursors interact with cells. Furin Promotes Tumor Progression, so this is where VAIDS becomes cancerous.
In addition, Furin enzyme is linked to the process of RGMc - a severe overload of hemochromatosis or severe iron-overload of cells. Hence why EDTA-chelation works in some/many cases. This is a main cause of the zombie-brain, ask someone with hemochromatosis what it is like to remain sane.
Not elegant of a bioweapon enough for you yet? We have not even gotten to what happens once infection begins and the RNA instructions reverse transcribe themselves into your DNA and all your progeny’s DNA as well.
Digitizing Biology with Military Precision
Codons, Transposons, Mutagenesis and Nucleic Acids (DNA-RNA-miRNA-siRNA)
So a virus attached to your cells and screwed up a few processes, so what? Step 3 is to highjack the cell and have your own cells create more of this toxin. In every gene therapy injection, there are unlimited seeds which then tell your cells to create infinitely more of these bioweapon seeds. So in truth, it is a self-propagating bioweapon using your own cells as the factory.
Not sure exactly where it started but military-funded scientist J. Craig Venter is a great place to start. His team mapped the human genome and found out what makes humans human. In this process, he started to understand knockout genes as well as transposons, a sequence of DNA that is able to insert itself at a new location in our genome. Venter and Clyde Hutchinson targeted the human genome through ‘site-directed mutagenesis’ (fancy word for modifying human DNA).
In January, 2011, Venter told a military-packed auditorium at the NASA Ames Research Center “Nothing excites me more than trying to design organisms, even people for long-term space flight and even colonization of other worlds… Life is a DNA software system… the first step (to creating synthetic life) was making software that could build it own hardware…” Yes, J. Craig Venter created life and only a few even made a peep; he explained it away easily “creation of a bacterial cell controlled by a chemically synthesized genome”. And where did the “vaccine” spike protein sequence come from? Oh yes, a computer in China. // snark // Enjoy becoming a snake (best case). I digress.
After creating life, Venter went on to convert one species to another. His team modified the chromosome of one bacteria and inserted its “modified RNA instructions” into another species of bacteria. The mRNA instructions started creating enzymes that killed the host bacterium. “We transplanted the genome from one cell into another species, and in the process of doing that, converted the one species into the other” - he quipped cheerfully. And ‘you’ motherfuckers want me to take an mRNA vaccine?
Venter goes on to discuss metabolomics (which I believe is the end-end-game) - “the best quantitation of our (human) chemistry is roughly 2,400 chemical compounds that we can make enzymatically from our gene set… so for using our imaginations, why not come up with a synthetic microbiome?… Why not add bacteria-cells that make specific nutrients or vitamins instead of having to get those from diet”. Later in the same discussion he readdresses creating organisms to produce methane based products (fossil fuels are not really fossils any longer) “we sequenced Methanococcus Jannaschii… a complete autotroph, it doesn’t need organic compounds. It makes everything it needs (and expels methane gas) from life from carbon dioxide and hydrogen as and energy source.” // more snark // Eat your mRNA lettuce, Daddy Starbucks needs a new oil industry to rule - the human synthetically created hydrocarbon market. ps - BP Oil funded much of his work.
I digress once again: Venter goes on to discuss his work on transposon mutagenesis with co-scientist-nut Clyde Hutchinson - “transposons are these small pieces of DNA that jump around in genetic code. Over half of our human genome is composed of these transposons. They’re constantly jumping around and if they jump into the middle of a key gene, we can get a disease or next generations won’t exist with these.”
“And the exciting phase came, we inserted this piece of inert chemical in to E. coli (this is using your lymphatic system the same way) and the E. coli genome system started reading this piece of DNA (mRNA) and started making all the proteins. The proteins self-assembled to make the virus and the virus showed its gratitude by killing the cells that made it. So this is a situation where the software (mRNA) is actually building its own hardware. All we did was put in a chemical piece of software and it led to making this a physical structure that has biological activity.”
Eloquent enough of a bioweapon yet? What are the mRNA instructions telling your cells to create? PKM Zeta is for sure one chemical compound being manufactured in your cells - so enjoy forgetting if you are jabbed. Continue down the rabbit hole.
Military Science - Winning the War by Controlling the Mind Battlefield
Luciferase and neural mesh being built by the mRNA gene therapies. Not sure if they intended to kill so many people, as their true intent has always been to tap into your mind. Do not think for one second that the launch of over 1,000 orbiting microwave emitting satellites by Leon Skum (Elon ‘the Military Mouse’ Musk) and his neuralink are not all connected. The US Military’s motto has always been “winning their hearts and minds…”, well they told you.
By taking this bioweapon, you now have various sensors and transmitters positioned all around your body. You are now attached to Skynet and AI silicon can tell every thought and impulse. It can reveal all of your actions and consumptions by the chemicals under your skin. And Neuromem is graphene oxide building a little storage device, so they can keep a record of your mind’s good and bad deeds.
Psycho-Neurobiology and the battlefield of the mind. In a April 2018 lecture to the US Military Academy at West Point, CIA/military neurobiologist Dr. Charles Morgan gave an excellent description of where we are at in the current biological warfare scape. His “estimate of what is going to happen over the next five years (today)”:
Mind, Body and Beyond
“you can have a brain here, in the US plugged in, running a mechanical device somewhere else in the world”
“if I can send motor function from a brain to a mechanical arm, is it possible to send motor functions from one human to another human?”
“the really fun part was that you are taking over somebody else’s physical body with the mind of a human”
“can you send and receive sensory information - like ‘The Matrix’? Short answer? Yes.”
“DARPA did get permission to do deep electrode implants… brain-to-brain transfer”
Biohacking
example: Chlorin e6 (Ce6) administered to eyes conferred ‘night vision’ and allowed humans to see over 16 feet in the dark
“possibility now is there to develop different kinds of devices… to have an extra ability to be able to see through walls, to see heartbeats… anything you can co-opt is theoretically now possible”
“as transcranial magnetic stimulation… as they refine the technology, you can get a better point specificity to the neurons you actually want to activate. You should be able to do this without penetrating the skull (5G)”
Gene Slicing
“this technology (J. Craig Venter’s) paired with something called CRISPR, just like an editing software for genes, makes a number of things immediately available”
“he programmed yeast cells to produce anything he wanted: they can produce perfume, they can produce petroleum… anything we program the DNA to do”
“you can engineer anything, you can engineer a unique thing that would only kill one person in the world”
“what would you do with this if you were in security and intelligence?
DREADDs - Designer Receptors Exclusively Activated by Designer Drugs
Induced neuron bursts (via 5G), silence neurons, increase c-AMP (brain intercellular messengers)
“So think about it: you can create a cell, you can put it somewhere in the body, and you can remotely activate it when exposed to the right signal”
“So you have the capacity to create ANY product as long as you know the DNA sequence. You can insert it into a living system and you can remotely control it.”
“if I want a product produced in your brain that may affect the way you think, the way you act; one route to that is through stem cells (embryonic stem cells used in the “vaccines - haha”)… the potential unlike other cells in your body to become anything… to park there and do the work you’d like them to do”
DNA Encryption
Bacterial hard drives - using human microbiome or endocrine system
DNA cryptography
Asymmetric Encryption and Signature - merging quantum based computers with wet-DNA (human)
The Past is Not What it Used To Be and Memory
Men in Black “neuralizer” is real
PKMzeta and ZIP - washes the hippocampus of the brain
And finally, my personal favorite, long-term CIA/military neurobiologist Dr. James Giordano. Clap, clap, clap… Giordano is actually Telly Savalas’ ‘Ernst Stavro Blofeld’ in ‘On Her Majesty's Secret Service’.
Dr. Giordano gave this wonderfully psychotic speech at ‘Mad Scientist 2017 Georgetown’, where he explains that he sits on the ethics board for the technology and science he and DARPA create and pioneer. Foxes counting the hens.
Greasy, fast-talking-fucker but here are a list of my favorite quotes:
“I spend half of my time in Bavaria”
“other areas of science and technology in concentrated agenda called ‘Advanced Scientific Integrated Technologies’ or convergences… a whole host of capabilities under a broad rubric of brain science… bioscience and technology, pharmacology, engineering, genetics; this all falls under the rubric of an integrated neuroscience.” aka - his science over the last 40 years.
“A, A, A. That’s what the brain sciences do: allow Access to the brain, allow us to Assess the brain, and allow us to Affect the brain.”
“in somewhat military terms, the availability of reconnaissance methods then allows an increased viability for targeting methods. That’s what the brain sciences allow us to do”
“brain sciences… to affect human relations on a variety of scales, try to optimize those relations, in some cases and in others try to streamline those relations in ways that are commensurate with national security intelligence and defense interests”.
“value of neuro scientific tools and technologies to then be able to influence various postures and stances that are affected by individuals’ brains through their functions of cognitions, emotions and behaviors, with regards to those things that realm within the operational sphere of both politics in the military”.
“anything that I use to affect you in any way is a weapon… we are using it in the meliorate of sensors so as to be able to alter their behavior in a means of contending against another”.
“now what we’re doing is advancing neuroscience and technology and their conventional silos of operational use within medicine, within the public domain, within the commercial domain - so as to gain economic leverage on global market stages as well as direct use within intelligence and psychological operations”
“that’s a nice way of saying ‘I can affect minds to affect hearts’”
“now let’s turn the page, that’s soft weapons. Neuroscience can also be used as more conventional hard weapons… bioweapons in general. This is primarily chemicals, biologicals and devices. Or, as we like to say: drugs, bugs, toxins and tools.”
“more and more you hear the idea of ‘enhancement’ being bantered around a variety of different flora… the realities of what I am telling you here are not science fiction, they are science fact that are poised for operational engaged within the next 60 calendar months”
“work, for example… (we) are engaging certain forms of prosthetics that change the sensibilities and sensitivities of a variety of our different sensoria; for example ‘eye’, ‘ear’ and ‘touch’… we can modify these sensory to essentially make an individual have what’s called ‘bat ear’, ‘dog’s nose’, ‘bird’s eye’. So what we can do is take the normal individual… and modify that so now we may have an individual who is now able to see on a broader spectrum of light… an individual that can hear hypersonically or ultrasonically. An individual that has higher tactile sensibilities and sensitivities…”
My favorite Giordano slide to end on:
Watch the video in awe.
Research - just in case anyone cares where I got the info...
https://open.substack.com/pub/inugo/p/the-elegant-bioweapon-research?r=qx9b5&utm_campaign=post&utm_medium=web
A big thank you!