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How DARPA and Moderna pioneered the idea behind mRNA vaccines

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DARPA has openly bragged on Twitter that Moderna’s mRNA vaccine technology, and by extension Moderna’s Covid vaccine, was a product of their ADEPT program.

Below, Spartacus takes a look at the paper trail that shows Moderna is just another front in the Biodefence Mafia.

The introduction of foreign nucleic acids – RNA or DNA – into the body to generate foreign proteins is, by definition, gene therapy, regardless of whether or not the subject’s own genes are changed by it.

Cationic lipids, like the lipid nanoparticles used in mRNA vaccines, are capable of transfecting basically any type of cell with instructions to make proteins.  If the immune system catches a cell producing non-human proteins, some seriously bad things will happen to that cell.

There has been a major push for the adoption of nucleic acid vaccine tech in prior years, largely hidden from the public eye. In order to begin tracing it out, one must simply perform date range searches for the years prior to 2020, for nucleic acid vaccines. The cheerleaders of this technology immediately reveal themselves. And they are all looking for technology that is easy, rapid, and cost-effective for development and manufacture.

Naturally, the military would be interested in this technology for quickly vaccinating large populations of people against bioweapons ahead of pandemic spread, because it offers the potential for rapid development and deployment of countermeasures in a wartime scenario with equally rapid-developed bioweapons being flung all over the place.  This is where DARPA’s ADEPT comes in.

DARPA openly brag on Twitter that Moderna’s mRNA vaccine technology, and by extension Moderna’s Covid vaccine, was a product of ADEPT.  As Stat News reported:

“A review of dozens of patent applications found [Moderna] received approximately $20 million from the federal government in grants several years ago and the funds “likely” led to the creation of its vaccine technology. This was used to develop vaccines to combat different viruses, such as Zika and, later, the virus that causes Covid-19.”

Corporate media, with few exceptions, are largely silent on this matter.  The reason you have been kept in the dark is because you are the target of a globe-spanning military operation, with population reduction, mass surveillance, tyrannical control of people’s movements, and the destruction of human autonomy through implanted technology as its end goal.

Related: The real reason Moderna is suing Pfizer – Moderna helped create Covid-19 & patented “Virus” in 2013; allowing Moderna to develop a Covid Vaccine before world knew Covid-19 even existed


Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox…


By Spartacus

Nucleic Acid Vaccines

A nucleic acid vaccine is a vaccine that uses gene delivery methods, such as lipid nanoparticles or viral vectors, to deliver some quantity of either DNA or RNA into a cell. The cell’s own machinery, in the form of RNA polymerases and ribosomes, uses these nucleic acids as instructions to synthesize proteins. In the case of a nucleic acid vaccine, the protein in question is usually one of the structural proteins of a virus, with the aim of generating an antibody response against that specific protein, but this isn’t the only type of product that nucleic acid transfection can produce. Gene transfection into cells can, in fact, make those cells produce any kind of protein, with the right instructions, including monoclonal antibodies, designer receptors, anything imaginable.

In the case of the Covid-19 vaccines, the media and the medical establishment tried getting around this by arguing that since the vaccines did not change the recipient’s DNA, that meant that they weren’t gene therapy. The introduction of foreign nucleic acids into the body to generate foreign proteins is, by definition, gene therapy, regardless of whether or not the subject’s own genes are changed by it. DNA and RNA are genetic material, and if the immune system catches a cell producing non-human proteins, some seriously bad things will happen to that cell.

Unlike a virus – which only binds to specific host factors expressed by specific cell lines and is endocytosed in those specific cells – cationic lipids, like the lipid nanoparticles (“LNPs”) used in mRNA vaccines, are capable of transfecting basically any type of cell with instructions to make proteins. LNPs were investigated for many years as a means of delivering Alzheimer’s drugs to the brain because they readily bypass the blood-brain barrier.

When the thing being delivered is a toxin, like SARS-CoV-2 Spike, however, there are serious consequences.

MDPI – A Case Report: Multifocal Necrotizing Encephalitis and Myocarditis after BNT162b2 mRNA Vaccination against Covid-19:

The current report presents the case of a 76-year-old man with Parkinson’s disease (PD) who died three weeks after receiving his third Covid-19 vaccination.

The patient was first vaccinated in May 2021 with the ChAdOx1 nCov-19 vector [AstraZeneca] vaccine, followed by two doses of the BNT162b2 mRNA [Pfizer-BioNTech] vaccine in July and December 2021.

The family of the deceased requested an autopsy due to ambiguous clinical signs before death. PD was confirmed by post-mortem examinations. Furthermore, signs of aspiration pneumonia and systemic arteriosclerosis were evident. However, histopathological analyses of the brain uncovered previously unsuspected findings, including acute vasculitis (predominantly lymphocytic) as well as multifocal necrotising encephalitis of unknown aetiology with pronounced inflammation including glial and lymphocytic reaction. In the heart, signs of chronic cardiomyopathy as well as mild acute lympho-histiocytic myocarditis and vasculitis were present.

Although there was no history of Covid-19 for this patient, immunohistochemistry for SARS-CoV-2 antigens (spike and nucleocapsid proteins) was performed. Surprisingly, only spike protein but no nucleocapsid protein could be detected within the foci of inflammation in both the brain and the heart, particularly in the endothelial cells of small blood vessels.

Since no nucleocapsid protein could be detected, the presence of spike protein must be ascribed to vaccination rather than to viral infection. The findings corroborate previous reports of encephalitis and myocarditis caused by gene-based Covid-19 vaccines. [emphasis our own]

There has been a major push for the adoption of nucleic acid vaccine tech in prior years, largely hidden from the public eye. In order to begin tracing it out, one must simply perform date range searches for the years prior to 2020, for nucleic acid vaccines. The cheerleaders of this technology immediately reveal themselves.

Easy, Rapid, Cost-Effective Development and Manufacture

Nature – mRNA vaccines — a new era in vaccinology:

mRNA vaccines represent a promising alternative to conventional vaccine approaches because of their high potency, capacity for rapid development and potential for low-cost manufacture and safe administration. However, their application has until recently been restricted by the instability and inefficient in vivo delivery of mRNA.

Recent technological advances have now largely overcome these issues, and multiple mRNA vaccine platforms against infectious diseases and several types of cancer have demonstrated encouraging results in both animal models and humans. This Review provides a detailed overview of mRNA vaccines and considers future directions and challenges in advancing this promising vaccine platform to widespread therapeutic use. [emphasis our own]

Frontiers – Advances in mRNA Vaccines for Infectious Diseases:

During the last two decades, there has been broad interest in RNA-based technologies for the development of prophylactic and therapeutic vaccines.

Preclinical and clinical trials have shown that mRNA vaccines provide a safe and long-lasting immune response in animal models and humans. In this review, we summarise current research progress on mRNA vaccines, which have the potential to be quick-manufactured and to become powerful tools against infectious disease and we highlight the bright future of their design and applications. [emphasis our own]

International Journal of Nanomedicine – Development of nucleic acid vaccines: use of self-amplifying RNA in lipid nanoparticles:

Self-amplifying RNA or RNA replicon is a form of nucleic acid-based vaccine derived from either positive-strand or negative-strand RNA viruses. The gene sequences encoding structural proteins in these RNA viruses are replaced by mRNA encoding antigens of interest as well as by RNA polymerase for replication and transcription. This kind of vaccine has been successfully assayed with many different antigens as vaccine candidates, and has been shown to be potent in several animal species, including mice, nonhuman primates, and humans.

A key challenge to realising the broad potential of self-amplifying vaccines is the need for safe and effective delivery methods. Ideally, an RNA nanocarrier should provide protection from blood nucleases and extended blood circulation, which ultimately would increase the possibility of reaching the target tissue.

The delivery system must then be internalised by the target cell and, upon receptor-mediated endocytosis, must be able to escape from the endosomal compartment into the cell cytoplasm, where the RNA machinery is located, while avoiding degradation by lysosomal enzymes. Further, delivery systems for systemic administration ought to be well tolerated upon administration. They should be safe, enabling the multi-administration treatment modalities required for improved clinical outcomes and, from a developmental point of view, production of large batches with reproducible specifications is also desirable.

In this review, the concept of self-amplifying RNA vaccines and the most promising lipid-based delivery systems are discussed. [emphasis our own]

Nature Gene Therapy – The promise of nucleic acid vaccines:

Establishing the effective use of ‘naked’ nucleic acids as vaccines would undoubtedly be one of the most important advances in the history of vaccinology.

While nucleic acids show much promise for use as vaccine vectors in experimental animals, not a single naked nucleic acid vector has been approved for use in humans. Indeed, data from human clinical trials is scant: nucleic acid vaccines have not been clearly demonstrated to have any convincing efficacy in the prevention or treatment of infectious disease or cancer.

Here we illustrate possible mechanisms underlying effective nucleic acid vaccination. We focus on progress that has been made in the improvement of their function. Additionally, we identify promising new strategies and try to forecast future developments that could lead to the real success of nucleic acid vaccines in the prevention and treatment of human disease.

Cell Press Molecular Therapy – Self-Amplifying RNA Vaccines Give Equivalent Protection against Influenza to mRNA Vaccines but at Much Lower Doses:

New vaccine platforms are needed to address the time gap between pathogen emergence and vaccine licensure. RNA-based vaccines are an attractive candidate for this role: they are safe, are produced cell free, and can be rapidly generated in response to pathogen emergence.

Two RNA vaccine platforms are available: synthetic mRNA molecules encoding only the antigen of interest and self-amplifying RNA (sa-RNA). sa-RNA is virally derived and encodes both the antigen of interest and proteins enabling RNA vaccine replication. Both platforms have been shown to induce an immune response, but it is not clear which approach is optimal.

In the current studies, we compared synthetic mRNA and sa-RNA expressing influenza virus hemagglutinin. Both platforms were protective, but equivalent levels of protection were achieved using 1.25 μg sa-RNA compared to 80 μg mRNA (64-fold less material). Having determined that sa-RNA was more effective than mRNA, we tested hemagglutinin from three strains of influenza H1N1, H3N2 (X31), and B (Massachusetts) as sa-RNA vaccines, and all protected against challenge infection. When sa-RNA was combined in a trivalent formulation, it protected against sequential H1N1 and H3N2 challenges. From this we conclude that sa-RNA is a promising platform for vaccines against viral diseases. [emphasis our own]

Again and again, the same properties are touted; easy, rapid, cost-effective development and manufacture. Plug in a gene sequence for the targeted antigen and away you go.

Naturally, the military would be interested in this technology for quickly vaccinating large populations of people against bioweapons ahead of pandemic spread, because it offers the potential for rapid development and deployment of countermeasures in a wartime scenario with equally rapid-developed bioweapons being flung all over the place.

ADEPT: PROTECT

ADEPT is a Defence Advanced Research Projects Agency (“DARPA”) program that began in 2012. The acronym stands for Autonomous Diagnostics to Enable Prevention and Therapeutics. PROTECT is a sub-program of ADEPT, and it stands for Prophylactic Options to Environmental and Contagious Threats.

Some quick searches reveal presentation slides about the project:

PROTECT provides prophylactic protection against disease by treating people with nucleic acid constructs that encode protective monoclonal antibodies.

And in the next image taken from a document titled ‘ADEPT:PROTECT’, “DARPA pioneered the use of the body as a bioreactor to produce prophylactic antibodies to protect against biothreats.”

Apparently, the goal of ADEPT: PROTECT was to come up with nucleic acid delivery systems that encoded monoclonal antibodies (or mAbs) against specific pathogens that may be used in biowarfare, such as influenza, smallpox, SARS, chikungunya, rabies, anthrax bacteria, and even ricin, nerve agents, and prions.

Antibodies are the means by which the adaptive immune system tags things for destruction and disposal. They lock over the surface proteins of pathogens and guide inactivated viruses and bacteria into leukocytes, encourage complement activation, and so on. Monoclonal antibodies are essentially copies of one specific kind of antibody, for therapeutic use. This differs slightly from how mRNA vaccines have ended up being used; generating the target antigen protein instead, and letting the body manufacture antibodies against it.

In DARPA’s own words, they partnered with Moderna to produce mRNA-1944, a nucleic acid-encoded mAb against chikungunya:

In fact, DARPA openly brag on Twitter that Moderna’s mRNA vaccine tech – and, by extension, mRNA-1273 (Moderna’s Covid vaccine), was a product of ADEPT:

Another company involved in ADEPT is Ichor Medical Systems, a little-known company in San Diego specialising in electroporation gene delivery tech that partners with Pfizer, Janssen, and USAMRIID.

Ichor Awarded DARPA ADEPT: PROTECT Contract:

Ichor Medical Systems of San Diego has been awarded a contract through the Defence Advanced Research Projects Agency (DARPA) and supported by the US Army Research Office for up to $20.2 million of funding over five years, including a base period award of $8.6M.

The award is part of a DARPA program called Autonomous Diagnostics to Enable Prevention and Therapeutics: Prophylactic Options to Environmental and Contagious Threats (ADEPT: PROTECT) aimed at developing new platform technologies that could be safely and rapidly deployed to the US population and military personnel to provide immediate protection in the event of an infectious outbreak or biological weapons attack.

The program will fund the development and clinical assessment of Ichor’s TriGrid electroporation system as a DNA-based antibody delivery platform to produce protective antibodies for passive immunoprophylaxis.

What’s really going on, here? Why haven’t the media extensively covered the military think tank side of all of this, as well as DARPA’s enduring partnership with Moderna?

Moderna failed to disclose federal funding for vaccine patent applications, advocates say:

An advocacy group has asked the Department of Defence to investigate what it called “an apparent failure” by Moderna (NASDAQ:MRNA) to disclose millions of dollars in awards received from the Defence Advanced Research Projects Agency in patent applications the company filed for vaccines.

In a letter to the agency, Knowledge Ecology International explained that a review of dozens of patent applications found the company received approximately $20 million from the federal government in grants several years ago and the funds “likely” led to the creation of its vaccine technology. This was used to develop vaccines to combat different viruses, such as Zika and, later, the virus that causes Covid-19.

In arguing for an investigation, the advocacy group maintained Moderna is obligated under federal law to disclose the grants that led to nearly a dozen specific patent applications and explained the financial support means the US government would have certain rights over the patents. In other words, US taxpayers would have an ownership stake in vaccines developed by the company.

There is an extensive paper trail, here, one that shows that Moderna is just another front in the Biodefence Mafia. The media, with few exceptions, are largely silent on this matter.

If we are at war – and at this point, only an idiot would fail to see that we are – then who fired the first shot? Why are world leaders so tight-lipped about all of this? Well, it’s simple, really.

The reason why you have been kept in the dark is because you are the target of a globe-spanning military operation, with population reduction, mass surveillance, tyrannical control of people’s movements, and the destruction of human autonomy through implanted technology as its end goal.

In all of the affluent nations operating under the globalist managerial rules-based order of private-public partnerships, NGOs, and supranational organisations, the only real threats to the ruling class are resurgent nationalism, populism, and traditionalism, because these things invariably lead to protectionist economic policies that divert resources away from the already magnificently wealthy ruling class and towards the middle.

Populism is only a problem for the rich and powerful if there are people to embody it. No people, no problem. Hence the reliance on bioweapons and poisonous vaccines. The Neo-Malthusian ruling class want to kill off insolent, rebellious, resource-overconsuming plebeians, keep the valuable infrastructure intact, and profit off of it, after they corral just enough survivors to keep their global consumerist orgy going.

They aren’t even discreet about it. They openly revel in their extraordinarily grandiose ideas.

Carnegie Council for Ethics in International Affairs: Yuval Noah Harari, Workplace Automation & the “Useless Class”,
13 March 2017 (4 mins)

These people want to control you, and if they can’t control you, then they want to replace you with someone they can. The word for this condition is megalomania.

Merriam-Webster – Megalomania:

meg·​a·​lo·​ma·​nia ˌme-gə-lō-ˈmā-nē-ə  -nyə

1: a mania (see MANIA sense 2a) for great or grandiose performancean outburst of wildly extravagant commercial megalomania The Times Literary Supplement (London)

2: a delusional mental illness that is marked by feelings of personal omnipotence and grandeur

megalomaniac ˌme-gə-lō-ˈmā-nē-ˌak  adjective or noun

megalomaniacal ˌme-gə-lō-mə-ˈnī-ə-kəl  adjective or less commonly megalomanic ˌme-gə-lō-ˈma-nik 

megalomaniacally ˌme-gə-lō-mə-ˈnī-ə-k(ə-)lē  adverb

We must throw all of our energy into exposing these people and dismantling their tyrannical institutions. As they have clearly violated the social contract and are scrambling desperately to conceal that fact, there is no point whatsoever in obeying them. Their authority is now illegitimate.

We have every right to defend ourselves and our kin from murderous despots who plot against us in the dark.

Featured image: Advanced Weapons Developer D.A.R.P.A. Invested $25M in Moderna’s mRNA Vax in 2013, American Faith, 19 August 2021

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GundelP
GundelP
1 month ago

YAWN, sorry, the usual stuff, half truth half made up stuff or simply lies. Still better to them than let the ppl to learn some truth about biology.

There are NO bioweapons but only poisons, they can’t really mess with bacteria because it behaves very differently in a petri dish compared to a whole living system.

I knew for a while that the big mysteries connected to water I just didn’t now how.

A bit complicated here and there but this is (it looks) the base knowledge and unlike viruses or germ theory it is supported by proofs, many.

https://www.youtube.com/watch?v=yBjlBcPbGJs



GundelP
GundelP
Reply to  Rhoda Wilson
1 month ago

I don’t know Rhoda, poisons like the graphene vax and tests? Neither I nor you can’t go in any to check what’s going on, on the other hand we were told so many tales, so many deception.

Did you know that even the nuclear bomb part is not ‘settled’? We learnt in school, and probably you too, that there is a thing called ‘half-life’ according to that the level of ionizing radiation released should have made Hirosima and Nagasaki unfit for life for hundreds if not thousands of years, but ppl live there and look well enough.

Than how can you know that anything they tell about biolabs are true? They must keep us in fear, war on terrorism, covid, bio attack, to keep us in line and them in power.

One thing I know for sure. I followed Rappoport for years, behind every ‘pandemic’ there was a poison or even more, they were invented to disguise it, no exception.

Show me a bioweapon, bacteria or virus based where there is proof but only parroting about it. Same true for the spike protein.

GundelP
GundelP
Reply to  Rhoda Wilson
1 month ago

I use my own mind Rhoda and have a really bad habit, I demand proof, always, before believing anything, no matter who and how many times parrots it, if no proof I won’t handle it as fact.

  • There is zero proof for pathogenic viruses, what they call viruses are exosomes, proven by many source what you – this site – somehow not really fancy. There is an ongoing big virus debate, debate is not the best world because the virus-believers didn’t dare to go into this discussion. NONE OF THEM, not even one. Oh, I am wrong, Dr Yeadon finally did, he admitted that they didn’t know what caused respiratory illnesses but couldn’t be viruses. Since then I haven’t heard a word about him, none, not even here.

Just a single search on virus-debate and the search engine will miss many related articles but still many-many will be showed. Did you bother to have look, Rhoda?
https://truthcomestolight.com/?s=virus+debate

Their role? Messengers. In the nature things work in an analogue way. Study how trees and shrubs work if you don’t know what I am talking about, when they send chemical warnings if an animal start to chew them.

  • Biolabs is only a name, I wrote they could experiment on poisons or even on biological material but there is a glitch, they CAN’T modify biological material to become a weapon. I asked you show me a bacteria or virus where there is proof that they modified it and caused something with it. Where is it? Or where is the spike protein out of Photoshop and drawings? Can you show it?

And you really haven’t read Rappoport? Probably not because if you would have read him you would know that he always gives proof to his statements, no exception.
He wrote the book AIDS Inc more than 30 years ago, if ppl bothered to read it they would have recognize the similarities the fraudulent test and poisoning which happened in the name of covid. But I guess your opinion about biolabs and 4th level security and all of the BS based on Hollywood’ conditioning movies.

  • Vaccines are poisons, including even the ones against bacteria but to understand this you (again) should fetch some time to see the proof. Like Dr Humpries lecture on tetanus.

I try to link it but I doubt you would bother to watch it to widen the spectrum of your knowledge. While it could save your life and many more people’s…

GundelP
GundelP
Reply to  GundelP
1 month ago

But if you are short on time, just watch this but really, how you can be a journalist with such a shallow knowledge? Sorry. But you have time 3 articles / day, together with proper research? Wow, I keep thinking on that Rhoda is one person or rather a unit, brigade under one name.

https://truthcomestolight.com/the-end-of-germ-theory-documentary-an-easy-to-understand-step-by-step-analysis-of-the-history-of-germ-virus-theory-the-erroneous-science-behind-vaccination-a-close-look-at/

CAN YOU COUNT THE WORD FAILED? THEN READ AND WATCH THE REST….

00:01:21 Dr Rosenau / US Public Health Service failed Spanish Flu contagion experiments
00:08:14 Goat Island / US Public Health Service failed Spanish Flu contagion experiments
00:10:32 Johns Hopkins / Dr Sellard failed Measles contagion experiments
Dr. Alfred F Hess failed Chicken Pox varicella contagion experiments
00:12:25 NY State Health Department / US Public health Service failed Polio contagion
experiments
00:15:13 Dr. Eleanor McBean vaccination caused Spanish Flu pandemic research
00:16:06 Dr Frederick Lamont Gates / US Army Antimenigitis vaccination fiasco
00:17:00 Black Death, Spanish Flu outbreak follows 14-25 vaccinations per person
00:21:30 Unvaccinated doctors and families did not catch the Spanish Flu from patients
00:23:05 Masha & Dasha, conjoined twins who never caught flu, colds, measles from eachother
00:24:17 What is Polio really? Lead Arsenate and DDT trends vs outbreaks
00:27:35 False vaccine disease eradication claims and trends
00:28:44 7 common causes of Polio
00:29:14 What is a “virus particle”?
00:32:47 What is Cytopathic Effect “Theory”?
00:33:22 What is Viral Replication “Theory”?
00:38:28 What is a virology cell or tissue “Culture”?
00:42:00 Cytopathic Effect Theory debunked
00:42:40 Autolysis and Apoptosis
00:44:48 Virus particle Isolation and Purification
00:55:38 PCR test fraud and misuse
01:06:54 CDC Covid PCR diagnostic test fraud
01:08:50 “Insilico” imaginary genomes
01:16:50 John Enders’ debunked Measles experiments
01:23:34 Studies admitting virus particles are indistinguishable from cellular debris
01:29:18 Fraudulent Australian failed Covid isolation experiments
01:32:13 Fetal Bovine Calf Serum RNA
01:34:28 Dr Stefan Lanka control experiments debunk virus theory once and for all
01:47:20 1947 fraudulent Polio isolation experiments debunked
02:01:28 Virology fails Koch’s postulates
02:02:59 Antibodies, Antigen test fraud, HIV
02:11:35 Antibody vaccine theory debunked
02:16:38 Big Pharma re-name disease game
02:16:54 Monkeypox fraud
02:22:51 Real causes of Pox diseases
02:24:28 1957 Monkeypox failed contagion experiments and controls debunk virology
02:31:49 Why do some but not all people sometimes but not always seem sick together?

OzzieThinker
OzzieThinker
Reply to  GundelP
1 month ago

Interesting added feedback GundelP. I have taken note.

In my opinion Bechamp was correct. Our whole “understanding” of how viruses are transmitted (and what they are) is plain wrong (per modern “Pasteurianism”). Therefore mRNA and other technologies are doomed to failure. According to the ancients (esoteric knowledge) the body operates under the Luciferian System. This is a glorious recycling project whereby we either expel unwanted invaders, assimilate useful “nutrients”, contain questionable debris or die.

Though I wasn’t present at the first nuclear tests, it is clear we never have been able to “split” an atom, for that is impossible (atoms are interdimensional platforms which express themselves in a particular way in our reality). Indeed, though Oppenheimer predicted he might collapse all matter, all he did was disorganise the rhythm of targeted particles, which caused implosions (the explosions was an “outward” chain reaction).

So, there is much we aren’t told, there’s still a hell of a lot more we DON’T KNOW, contrary all these various propagandas.

Thank you again for your intelligent words.

GundelP
GundelP
1 month ago

This is a nice one, here comes their favorite ‘bioweapon’, arsenic aka anthrax.

“‘ARSENIC POISONING
Gradually, use of the anthrax vaccine faded. . . but here’s the mysterious thing: The occurrence of anthrax faded also. Today, it is a rare disease. So what was causing the death of so many animals, mostly sheep, during the nineteenth century, and why don’t sheep die of anthrax today?
Let us consider sheep dip (a liquid prepa­ration for cleansing sheep of parasites). The world’s first sheep dip—invented and produced by George Wilson of Coldstream, Scotland in 1830—was based on arsenic powder. One of the most successful brands was Cooper’s Dip, developed in 1852 by the British veterinary surgeon and industrialist William Cooper. Cooper’s dip contained arsenic pow­der and sulfur. The powder required mixing with wa­ter, so naturally agricul­tural workers—let alone the sheep dipped in the arsenic solution—were sometimes poisoned.

comment image

The symptoms of arse­nic poisoning are remark­ably similar to those of “anthrax,” including the appearance of black skin lesions. Like anthrax, arse­nic can poison through skin contact, through inhalation and through the gastroin­testinal tract. If an injection contains arsenic, it will cause a lesion at the site.
Sheep dips today no longer contain arsenic, so anthrax has disappeared—except in develop­ing countries where it is still an ingredient in industrial processes like tanning—hence the 2008 death of the drum maker working with imported animal skins.1″

Marty
Marty
1 month ago

DARPA exists for one person on this planet. The antichrist. Nothing more nothing less. Their job? To murder, or to change mankind.

trackback
1 month ago

[…] The Exposé – Rhoda Wilson, 15 ott 2022 […]

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1 month ago

[…] How DARPA and Moderna pioneered the idea behind mRNA vaccinesDARPA has openly bragged on Twitter that Moderna’s mRNA vaccine technology, and by extension Moderna’s Covid vaccine, was a product of their ADEPT program. Below, Spartacus takes a look at the paper trail that shows Moderna is just another front in the Biodefence Mafia. […]

Bob
Bob
1 month ago

Hang Harari publoically, also the Rothschilds, Sassoon, Goldmans, Sachs, Schwab, and all the other jewish masterminds of the genocide.

Demeter
Demeter
1 month ago

Great article but personally believe we live in a simulation, where choices must be made. Believe without question, or question. I don’t just question,i don’t believe in what we perceive.

Might sound daft but just question everything, most of our beliefs are lies perpetuated to enforce compliance, with evil.