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  • Nate Serg

DONE AND DONE

Updated: Jul 30, 2021




Study: ‘Virus’ Is Identical to Normal Cell ‘Structures’


...Another nail in the coffin for the existence of SARS-CoV-2. The paper is titled “Appearances Can be Deceiving – Viral-like Inclusions in Covid-19 Negative Renal Biopsies by Electron Microscopy.” The authors are Clarrisa A. Cassol, et al., and the citation is Kidney360 1:824-828, 2020. This is a peer-reviewed journal affiliated with the American Society of Nephrology; in other words, this paper comes squarely from what is called acceptable, mainstream science.

Many of you have probably seen the electron-micrograph pictures of SARS-CoV-2, the ones in black and white, with the black dots within the faint outline of the circle. I have attached two such images from papers that claim these photos show direct evidence of the existence of the virus. These are the pictures that virologists show us, not the computer-generated, colorful images that you see in magazines and on the internet. These are the “real” pictures of the virus, and they are offered as “proof” that the virus exists.

However, it turns out these photos are actually NOT corona viruses, and the CDC, among others, has known this fact since at least 2004. The above paper examines the evidence used to claim that these images represent viruses, rather than normal “structures” within a cell, particularly sick cells. Here is what the paper says:


“We have observed morphologically indistinguishable inclusions within podocytes and tubular epithelial cells both in patients negative for coronavirus disease 2019 (COVID-19) as well as in renal biopsies from the pre-COVID-19 era” (emphasis added).


In other words, the researchers saw these same structures in people with no evidence of Covid and in samples they took before Covid even happened, before the virus was said to even exist.

In addition, they say:


“We postulated that endogenous mimickers could be present that are morphologically indistinguishable from SARS-CoV-2 virions ultrastructurally.”

And:

“Viral-like inclusions, consisting both of single vesicles with diameters between 50 and 138 nm, as well as packed groups within larger vesicles, were found in all 15 cases, either in podocytes. Tubular epithelia, or vascular epithelial cells (figure 1).”


In all 15 cases that they examined, they found structures identical to what is being called SARS-CoV-2. They were scattered all over the kidneys and blood vessels; they are not viruses, but normal parts of the cells.

Then they go on to describe how these particles come about:

“A number of potential natural mimickers that can generate intracellular groups of round vesicles mimicking

SARS-CoV-2 virions could be listed, the most likely being endocytic vesicles and endosomal components such as microvesicular bodies containing exosomes, among others. Endocytosis leads to the formation of 60-120 nm vesicles, which is within the size range described for SARS-CoV-2 (60-140nm). These endocytic vesicles may be coated by different proteins, one of the most common being clathrin. The presence of coating proteins may be responsible for the presence of an electron-dense area surrounding these vesicles, giving the appearance of a viral corona.”

In other words, remember the famous “corona” on the corona virus? It turns out it’s just a common protein coating on normal vesicles, picking up the dyes in the electron-microscope preparation. The corona appearance is just another creative fiction, dreamed up by virologists and their graphic design teams.

Finally, the paper goes on to say that, naturally, you see more of these particles in sick people than in healthy people, which is exactly what I have been suggesting this past year. Dead and dying cells make these particles in the dying process and partly to get rid of poisons.

But the final nail comes in this quote:

“The potential for confusion of coronavirus particles with normal cellular components was in fact highlighted in a detailed ultrastructural study by the Centers for Disease Control and Prevention (CDC) of SARS-CoV responsible for the 2003 SARS outbreak.”[1]

In other words, the CDC in 2004 knew that researchers couldn’t reliably know these particles were coronavirus particles. Not a word has been heard about this since. All virologists use these pictures as proof of the existence of this virus. It is a fraud, based on junk science, like everything else connected with “Covid 19.”



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(Note from e-mailer ; Not once have i seen any paper that does not use a cell cuture (Vero 6, or FBS with antibiotics ) to claim "isolation". From what is growing enormously evident, they have attempted to affrim the consequent or commited fraud. )



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Statement On Virus Isolation (SOVI)

Isolation: The action of isolating; the fact or condition of being isolated or standing alone; separation from other things or persons; solitariness.

– Oxford English Dictionary

The controversy over whether the SARS-CoV-2 virus has ever been isolated or purified continues. However, using the above definition, common sense, the laws of logic and the dictates of science, any unbiased person must come to the conclusion that the SARS-CoV-2 virus has been isolated or purified. As a result, no confirmation of the virus’ existence can be found. The logical, common sense, and scientific consequences of this fact are:

the structure and composition of something not shown to exist can’t be known, including the presence, structure, and function of any hypothetical spike or other proteins;

the genetic sequence of something that has never been found can’t be known;

“variants” of something that hasn’t been shown to exist can’t be known;

it’s impossible to demonstrate that SARS-CoV-2 causes a disease called Covid-19.

In as concise terms as possible, here’s the proper way to isolate, characterize and demonstrate a new virus. First, one takes samples (blood, sputum, secretions) from many people (e.g. 500) with symptoms which are unique and specific enough to characterize an illness. Without mixing these samples with ANY tissue or products that also contain genetic material, the virologist macerates, filters and ultracentrifuges i.e. the specimen. This common virology technique, done for decades to isolate bacteriophages1 and so-called giant viruses in every virology lab, then allows the virologist to demonstrate with electron microscopy thousands of identically sized and shaped particles. These particles are the isolated and purified virus.

These identical particles are then checked for uniformity by physical and/or microscopic techniques. Once the purity is determined, the particles may be further characterized. This would include examining the structure, morphology, and chemical composition of the particles. Next, their genetic makeup is characterized by extracting the genetic material directly from the purified particles and using genetic-sequencing techniques, such as Sanger sequencing, that have also been around for decades. Then one does an analysis to confirm that these uniform particles are exogenous (outside) in origin as a virus is conceptualized to be, and not the normal breakdown products of dead and dying tissues.2 (As of May 2020, we know that virologists have no way to determine whether the particles they’re seeing are viruses or just normal break-down products of dead and dying tissues.)3


If we have come this far then we have fully isolated, characterized, and genetically sequenced an exogenous virus particle. However, we still have to show it is causally related to a disease. This is carried out by exposing a group of healthy subjects (animals are usually used) to this isolated, purified virus in the manner in which the disease is thought to be transmitted. If the animals get sick with the same disease, as confirmed by clinical and autopsy findings, one has now shown that the virus actually causes a disease. This demonstrates infectivity and transmission of an infectious agent.

None of these steps has even been attempted with the SARS-CoV-2 virus, nor have all these steps been successfully performed for any so-called pathogenic virus. Our research indicates that a single study showing these steps does not exist in the medical literature.

Instead, since 1954, virologists have taken unpurified samples from a relatively few people, often less than ten, with a similar disease. They then minimally process this sample and inoculate this unpurified sample onto tissue culture containing usually four to six other types of material — all of which contain identical genetic material as to what is called a “virus.” The tissue culture is starved and poisoned and naturally disintegrates into many types of particles, some of which contain genetic material. Against all common sense, logic, use of the English language and scientific integrity, this process is called “virus isolation.” This brew containing fragments of genetic material from many sources is then subjected to genetic analysis, which then creates in a computer-simulation process the alleged sequence of the alleged virus, a so called in silico genome. At no time is an actual virus confirmed by electron microscopy. At no time is a genome extracted and sequenced from an actual virus. This is scientific fraud.

The observation that the unpurified specimen — inoculated onto tissue culture along with toxic antibiotics, bovine fetal tissue, amniotic fluid and other tissues — destroys the kidney tissue onto which it is inoculated is given as evidence of the virus’ existence and pathogenicity. This is scientific fraud.

From now on, when anyone gives you a paper that suggests the SARS-CoV-2 virus has been isolated, please check the methods sections. If the researchers used Vero cells or any other culture method, you know that their process was not isolation. You will hear the following excuses for why actual isolation isn’t done:

There were not enough virus particles found in samples from patients to analyze.

Viruses are intracellular parasites; they can’t be found outside the cell in this manner.

If No. 1 is correct, and we can’t find the virus in the sputum of sick people, then on what evidence do we think the virus is dangerous or even lethal? If No. 2 is correct, then how is the virus spread from person to person? We are told it emerges from the cell to infect others. Then why isn’t it possible to find it?

Finally, questioning these virology techniques and conclusions is not some distraction or divisive issue. Shining the light on this truth is essential to stop this terrible fraud that humanity is confronting. For, as we now know, if the virus has never been isolated, sequenced or shown to cause illness, if the virus is imaginary, then why are we wearing masks, social distancing and putting the whole world into prison?

Finally, if pathogenic viruses don’t exist, then what is going into those injectable devices erroneously called “vaccines,” and what is their purpose? This scientific question is the most urgent and relevant one of our time.

We are correct. The SARS-CoV2 virus does not exist.


1 Isolation, characterization and analysis of bacteriophages from the haloalkaline lake Elmenteita, KenyaJuliah Khayeli Akhwale et al, PLOS One, Published: April 25, 2019. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0215734 — accessed 2/15/21

2 “Extracellular Vesicles Derived From Apoptotic Cells: An Essential Link Between Death and Regeneration,” Maojiao Li1 et al, Frontiers in Cell and Developmental Biology, 2020 October 2. https://www.frontiersin.org/articles/10.3389/fcell.2020.573511/full — accessed 2/15/21

3 “The Role of Extraellular Vesicles as Allies of HIV, HCV and SARS Viruses,” Flavia Giannessi, et al, Viruses, 2020 May



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ONLY POISONED MONKEY KIDNEY CELLS ‘GREW’ THE ‘VIRUS’

Dr. Tom Cowan, October 2020


This week, my colleague and friend Sally Fallon Morell brought to my attention an amazing article put out by the CDC. The link to the article is here, and it was published in June 2020. The purpose of the article was for a group of about 20 virologists to describe the state of the science of the isolation, purification and biological characteristics of the new SARS-CoV-2 virus, and to share this information with other scientists for their own research. A thorough and careful reading of this important paper reveals some shocking findings.

First, in the section titled “Whole Genome Sequencing,” we find that rather than having isolated the virus and sequencing the genome from end to end, that the CDC “designed 37 pairs of nested PCRs spanning the genome on the basis of the coronavirus reference sequence (GenBank accession no. NC045512).”

To me, this computer-generation step constitutes scientific fraud. Here is an equivalency: A group of researchers claim to have found a unicorn because they found a piece of a hoof, a hair from a tail, and a snippet of a horn. They then add that information into a computer and program it to re-create the unicorn, and they then claim this computer re-creation is the real unicorn. Of course, they had never actually seen a unicorn so could not possibly have examined its genetic makeup to compare their samples with the actual unicorn’s hair, hooves and horn.

The researchers claim they decided which is the real genome of SARS-CoV-2 by “consensus,” sort of like a vote. Again, different computer programs will come up with different versions of the imaginary “unicorn,” so they come together as a group and decide which is the real imaginary unicorn.

The real blockbuster finding in this study comes later, a finding so shocking that I had to read it many times before I could believe what I was reading. Let me quote the passage intact:


“Therefore, we examined the capacity of SARS-CoV-2 to infect and replicate in several common primate and human cell lines, including human adenocarcinoma cells (A549), human liver cells (HUH 7.0), and human embryonic kidney cells (HEK-293T). In addition to Vero E6 and Vero CCL81 cells. … Each cell line was inoculated at high multiplicity of infection and examined 24h post-infection. No CPE was observed in any of the cell lines except in Vero cells, which grew to greater than 10 to the 7th power at 24 h post-infection. In contrast, HUH 7.0 and 293T showed only modest viral replication, and A549 cells were incompatible with SARS CoV-2 infection.”


What does this language actually mean, and why is it the most shocking statement of all from the virology community? When virologists attempt to prove infection, they have three possible “hosts” or models on which they can test. The first is humans. Exposure to humans is generally not done for ethical reasons and has never been done with SARS-CoV-2 or any coronavirus. The second possible host is animals. Forgetting for a moment that they never actually use purified virus when exposing animals, they do use solutions that they claim contain the virus. Exposure to animals has been done once with SARS-CoV-2, in an experiment that used mice. The researchers found that none of the wild (normal) mice got sick. In a group of genetically modified mice, a statistically insignificant number lost some fur. They experienced nothing like the illness called Covid 19.

The third method virologists use to prove infection and pathogenicity — the method they most rely on — is inoculation of solutions they say contain the virus onto a variety of tissue cultures. As I have pointed out many times, such inoculation has never been shown to kill (lyse) the tissue, unless the tissue is first starved and poisoned.

The shocking thing about the above quote is that using their own methods, the virologists found that solutions containing SARS-CoV-2 — even in high amounts — were NOT, I repeat NOT, infective to any of the three human tissue cultures they tested. In plain English, this means they proved, on their terms, that this “new coronavirus” is not infectious to human beings. It is ONLY infective to monkey kidney cells, and only then when you add two potent drugs (gentamicin and amphotericin), known to be toxic to kidneys, to the mix.

My friends, read this again and again. These virologists, published by the CDC, performed a clear proof, on their terms, showing that the SARS-CoV- 2 virus is harmless to human beings. That is the only possible conclusion, but, unfortunately, this result is not even mentioned in their conclusion. They simply say they can provide virus stocks cultured only on monkey Vero cells, thanks for coming.

If people really understood how this “science” was done, I would hope they would storm the gates and demand honesty, transparency and truth.



 

.... the mystery has not been completely solved yet. Until there is a formal published scientific manuscript, the facts can be argued, particularly regarding causality despite these facts having been officially announced. The data collected so far is not enough to confirm the causal relationship between the new‐type coronavirus and the respiratory disease based on classical Koch's postulates or modified ones as suggested by Fredricks and Relman.



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Claims vs. reality or facts


The virus has been isolated – not correct. The virus has never been isolated. (link)

The virus caused the COVID-19. No scientific or experimental evidence has been provided in support of this claim. (link)

The test detects or monitors the virus or infections. Not correct. The test has never been scientifically validated for the intended purpose. (link)

Masks protect from the virus – not valid. There is no scientific evidence available showing that the masks provide protection – none! (link)

Social distance provides protection. No scientific or experimental support is available in support of this claim. (link).

Vaccines are efficacious – not correct. No therapeutics or treatments have been tested (scientifically or experimentally) against "the virus." (link)

For further details, see here (link) or (link).


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REMINDER: "SARS-COV-2" has never been properly purified/isolated directly from a sick patient nor proven pathogenic by fulfilling Koch's Postulates.


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ISOLATION: the act of separating something from other things : the act of isolating something

https://www.merriam-webster.com/dictionary/isolation

This is the definition most people agree with and refer to when isolating something.

Not virologists. This is what virologists mean when using the word isolation:

“VIRUSES ARE BASICALLY INANIMATE OBJECTS WHICH NEED A CULTURE TO ACTIVATE IN. But the way they are phrasing the requests is that the sample must be COMPLETELY UNADULTERATED and not be grown in any culture – AND YOU CAN’T DO THAT,” she told AAP FactCheck in a phone interview.

“YOU CAN'T ISOLATE A VIRUS WITHOUT USING A CELL CULTURE, SO BY USING THEIR DEFINITION IT HASN'T BEEN ISOLATED. But it has been isolated and cultivated using a cell culture multiple times all around the world.”

https://www.aap.com.au/proof-the-virus-behind-covid-19.../

The above quote is from a FB "factcheck."

In layman's terms, if using the agreed upon definition of isolation, they agree that they haven't isolated a "virus" from everything else as that is impossible. But that's ok because it's a "virus." It needs a host cell (which should be from the host they take the "virus" from but try not to think too hard about that logical inconsistency) in order to grow and replicate. But not just any host cell will do. In the case of "SARS-COV-2," it needs the kidney cells from an African Green Monkey.

But wait, there's more!

It also needs to be immediately placed in "Viral" Transport Media after being taken from a patient. This normally consists of animal DNA, antibiotics, and other chemicals/nutrients. In order to grow, it needs fetal bovine serum (blood taken from the hearts of baby cows). In order to be free of bacteria, it needs 2 or 3 cell toxic antibiotics. In order to "eat," it needs various unknown nutrients/chemicals in DMEM. All of this must be added to the unpurified sample (which in and of itself contains billions of particles) from a patient, mixed together, and then incubated for days.

Once the expected Cytopathogenic Effect (i.e. cell death) is seen in the petri dish, then and only then has a "virus" been "isolated."

Virology subscribes to subtraction through ADDITION. Or, in other words, the EXACT OPPOSITE OF ISOLATION.

So once again, no "virus" has ever been properly purified nor ISOLATED.

This is how you FACTCHECK.

Related Post and Collection on Cell Cultures:

https://www.facebook.com/502548575/posts/10158078047703576/

https://m.facebook.com/story.php?story_fbid=10158191240103576&id=502548575

Figure 1: Actual Isolation

Figure 2: Virology "Isolation"


M.Stone - Isolation


For the in-depth death of Covid papers and Virology


Reader comment -

(They have never in WOLRD HISTORY taken an isolated and purified viral sample from a sick patient and directly proven that said sample can make another human sick...this has NOT been done in world history...ever..... all that they have is CPE in culture...this is their proof that viruses exist and are pathogenic....this is all that they have. )


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STEFFAN LANKA

"Viruses contained in vaccines Die Wurzel: Stefan, let's get back to the virus theory, which is the basis of vaccination. The vaccines used for measles, for example, are called "live" vaccines, although they are anything but living viruses.

How are "live" vaccines constructed and why should they simulate viruses when there are no viruses with independent infectious activity? "Living" and "dead" vaccines Stefan Lanka: Now I understand how you come up with the term "living" viruses. When tissues die in the laboratory during an "infection attempt" in the course of unintentional starvation and poisoning, the people involved believe that these tissues have been transformed into viruses or release viruses. Since the vaccine manufacturers (and their virologists) assume that the mass of dead tissue (i.e., their alleged viruses), which they use as a vaccine, is capable of infection, they speak of a "live vaccine".

They believe that the vaccination virus is still infectious but is attenuated. In contrast, that what is called "inactivated vaccines" is made from the components of alleged viruses; that is, they are not infectious or the decomposing tissue is protected from further decomposition by "preservatives" such as formaldehyde during an infection attempt, in order to use it afterwards as a "inactivated vaccine", as is the case with polio, for example. So: the idea of pathogenic viruses is dead and so is that of vaccination, so the question of "dead" or "alive" is not only misleading, but it is as wrong as the whole concept. Die Wurzel: And secondly, we know that such a "living" vaccine virus cannot occur in nature, so it is not comparable to a wild type of pathogen, right? Domestication of wild type viruses Stefan Lanka: The idea of a wild type of virus is not that of a particularly wild virus, but that the virus has just been spat out fresh from the hell of nature and must first be domesticated by "cultivation" in the laboratory in order to be made accessible for vaccination - science fiction, that is. Here we should also mention the particularly funny but profound article by Jochen Schamal "Kleine Vampirkunde" in the current issue of WissenschafftPlus 2/2020


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"It is important to mention that this unpurified mixture consisting of dying tissue and cells from monkeys, bovine foetuses and toxic antibiotics, is also being used as a “live” vaccine, because it is supposed to be composed of “attenuated” viruses. The death of tissue and cells – on account of starvation and poisoning and not because of an alleged infection – has continuously been misinterpreted as evidence for the existence of viruses, as evidence for their isolation and as evidence of their propagation.

Thus, the resulting toxic mixture full of foreign proteins, foreign nucleic acids (DNA/RNA), cytotoxic antibiotics, microbes and spores of all types is labelled as a “live vaccine”. It is implanted in children through vaccination mainly into the muscles, in a quantity which if it were injected into the veins would immediately lead to certain death. Only ignorant people who blindly trust in the state authorities who are “testing” and approving the vaccines can regard vaccination as a “small harmless prick”. The verifiable facts demonstrate the danger and negligence of these scientists and politicians, who claim that vaccines are safe, have little or no side-effects and would protect us from a disease. None of these claims is true and scientific, on the contrary: upon precise scientific analysis, one finds that vaccines are useless and the respective literature admits to the lack of any evidence in their favor.

2


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(Please check back as new content will get added to this document)

MIKE S - ISOLATION CHEATED



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7 ways to prove viruses don’t exist with Dr Stefan Lanka

Click this link for the document with illustrations for more clarity --- >



In all seven steps that virologists take to claim a virus, they refuse to adhere to the most important scientific duty, the verification of their methods: They never document control experiments! For this reason alone, statements by virologists claiming that viruses cause disease should never be considered scientific.


If you read the short methods and materials section of the supposedly scientific publications of the virologists, you will see that the virologists have refuted themselves with their explanations of the seven steps.

The ruling in the measles virus trial from 2012 to 2017 contains a meaning that goes beyond the measles compulsory vaccination: This jurisprudence removes the basis of the entire virology.

Dismantling the virus theory The “measles virus” as an example



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The 7 steps to prove viruses do not exist:

1. Virologists interpret the death of cells in the laboratory as viral. Due to the lack of control attempts (experiments), they overlook the fact that they kill the cells in the laboratory themselves and unintentionally by starving and poisoning the cells. This misinterpretation is based on a single publication by John Franklin Enders and a colleague from June 1, 1954. This publication was ruled by the highest court in Germany in the measles virus trial that it contained no evidence of a virus. This publication became the exclusive basis not only for measles virology, but for all virology since 1954 and corona hysteria.

Illustration:


CPE - Control Experiment - 21 April 2021 - English version 4/23/21

Dr Stefan Lanka, a marine & molecular biologist presents some results from the recent control experiments that have been made in regards to the cytopathic effect which "virologists'' look for in their experiments that attempt to prove the existence of "viruses''. The procedure used by all virologists to prove the existence & pathogenicity of so-called “viruses' ' has now been irrefutably debunked by virologist Dr. Stefan Lanka in his latest control experiments. Dr. Lanka reports on the initial findings of his control experiments showing that cell death (CPE) in the virologist’s lab has nothing to do with so-called “viruses'', but rather is due to the starving & poisoning of the cells as per standard protocol. These results officially refute virology.

This is just one control experiment of many where the results will later be published in a scientific journal.

It's time to write off "virology" as another failed hypothesis in the history of science. Interview with Dean Braus

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Video about the CPE Cyctopathic Effect Control Experiments

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2. Virologists mentally assemble the shortest pieces of so-called genetic information from dying cells to form a very long genetic strand, which they output as the genetic strand of a virus. This conceptual / computational process is called alignment. In doing so, they did not make the control attempts, the attempt to conceptually / computationally construct the desired genetic strand even from short pieces of so-called genetic information from non-infected sources.

Illustration:

3. For the alignment of a virus, virologists always need a given genetic strand of a virus. For this, however, they always use a genetically / computationally generated genetic strand and never a real one, one found in reality. In doing so, they never attempt to check whether or not so-called genetic information could also be constructed from the existing data set, including “viral” genetic material strands of completely different viruses.

Illustration:

Bioinformatics is nebulous. Bioinformaticians do not check whether the results of software processing are found in reality. What Bioinformaticians do is check something that doesn't exist in reality with something that doesn't exist in reality. Virology + Bioinformatics = Zero Science.

Illustration: picture number 3


4. Virologists have never seen or isolated “viruses” in humans, animals, plants or their fluids. They only did it seemingly, indirectly, and only ever by means of very special and artificial cell systems in the laboratory. They never mentioned the control attempts or documented whether they succeeded in depicting and isolating viruses in and from humans, animals, plants or their fluids.

Illustration:

5. Virologists have never isolated, biochemically characterized or obtained their supposed genetic material from the supposed viruses that they photograph using electron microscope images. They have never conducted or published control experiments as to whether, after isolating these structures, it was actually possible to detect “viral” proteins (the envelope of the virus) and, above all, the viral genome, which is supposed to be the central component and characteristic of a virus.

Illustration:

6. Virologists report typical artifacts of dying tissue / cells and typical structures that arise when the cell's own components such as proteins, fats and the solvents used are swirled, as viruses or viral components. Here, too, there are no control experiments with cells / tissues that were not infected but were also treated.

Illustration:

7. The so-called transmission attempts that virologists make to prove the transmission and pathogenicity of the suspected viruses refute the entire virology. Obviously, it is the experiments themselves that trigger the symptoms, which animal experiments provide as evidence of the existence and effectiveness of the suspected viruses. Here, too, there are no control attempts in which exactly the same thing is done, only with non-infected or sterilized materials.

Illustration: warning disturbing video.....

Please inform all relevant institutions in YOUR COUNTRY of these scientific facts. Ask them to inform all their employees. Ask your institutions to tell you if they have checked all of the above and informed their employees. Ask them to answer you as soon as possible. Give them SEVEN DAYS.

Try to understand this text, and YOU can write it in YOUR OWN words.

(SOURCE: translated from German and modified for citizens who are not citizens of the state of Germany.

https://rotekartefuercorona.de/drei-rote-karten.php

Pdf link to the 7 steps

https://wissenschafftplus.de/uploads/article/wissenschafftplus-virologists.pdf

Corona receives Three red cards

Tell your authorities that vaccination against alleged sars-cov-2 has no scientific basis. Together we make the house of cards coincide - show the authorities the red card

There is no emperor just his clothes - How to protect yourself and others-


All Corona measures are based on the Infection Protection Act (IfSG).

In §1, the IfSG demands the scientific nature of all those involved, including those of the virologists who claim the existence of the coronavirus SARS-CoV-2.

The virologists are clearly anti-scientific and have refuted themselves, which is why the IfSG is not fulfilled, but violated and therefore the legal basis for all corona measures is withdrawn.

In all seven steps that virologists take to claim a virus, they refuse to comply with the most important scientific duty, the verification of their methods: They never document control experiments! For this reason alone, statements by virologists claiming that viruses cause illness should never be considered scientific.

If you read the short methods and materials section of the supposedly scientific publications of the virologists, you will see that the virologists have refuted themselves with their explanations of the seven steps.

The ruling in the measles virus trial from 2012 to 2017 contains a meaning that goes beyond the measles compulsory vaccination: This jurisprudence removes the basis of the entire virology.

This is exciting news for humanity! The end of virology & vaccines is coming soon!


The complete fraudulent virology will soon be unmasked on the example of the computer conversion of parts of the alleged HIV into alleged Sars-cov-2. The end of the scam!

An example of creating the genome of the alleged sars-cov-2 from the sequences of the alleged HIV will destroy the complete fraudulent virology. SOON!

The point is that parts of alleged HIV cannot be parts of alleged Coronavirus at the same time. But that is exactly the case!

You all know that virologists do not isolate an alleged “viral” particle because it does not exist. Here's another piece of evidence: Virologists are rapidly moving to bizarre collections of genetic material after a procedure of mixing or contamination with animal RNA. The total RNA is extracted not from the alleged viral particle, which would be logical, but from BALF or CC - supernatant. Now let's look at what the scientific publication that is the basis of the corona scandal says:

"Bronchoalveolar-lavage fluid samples were collected in sterile cups to which virus transport medium was added."

"VIRAL GENOME SEQUENCING

RNA extracted from bronchoalveolar-lavage fluid and culture supernatants was used as a template to clone and sequence the genome."


Fetal Bovine Serum (FBS) is one of the sources of genetic contamination in studies that fraudulently allege to have "isolated SARS-COV-2". 4/2/21

Fetal Bovine Serum RNA Interferes with the Cell Culture derived Extracellular RNA


And see the ingredients in the CDC's SOP#: DSR-052-05 for "viral transport medium", which patient samples are often stored in before even getting to a lab for a useless PCR test, or fraudulent "isolation" procedures.


Here is the measles control experiment that has been robot translated. Important to note that this is written by the head of one of the 2 independent laboratories that made the experiments. 4/2/21

The experiments of Enders on the Track

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The final rebuttal of virology. English version. 6/3/21

THE REST OF THIS AMAZING ARTICLE / COMPLATION HERE

STEFFAN LANKAS CONTROL EXPERIMENTS AND VIRUS MYTH BREAKDOWN



SHOW US THE VIRUS PAGE ON COURT CASE AGAINST THE EXISTENCE OF SARSCOV2

THE FILES AND DOCUMENTS GOING INTO THE COURT CASE AGAINST THE EXISTENCE OF SARSCOV2 ------> https://www.showusthevirus.info/about-3


DR. Saeed Qureshi -


Tom video break down


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“If I could live my life over again, I’d devote it to proving that germs seek their natural habitat, disease tissue, rather than being the cause of disease tissue.”

-Dr. Rudolph Virchow, renowned scientist, considered the ‘Father of Pathology’


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All Mike Stone Coronavirus papers


Mike Stone document links


LACK OF "SARS-COV-2" ANIMAL MODEL:

https://docs.google.com/document/d/e/2PACX-1vRmYnE5xecj4Mbh3coSN8SObCeqPVD-vQz61HZsGIO5WIdcBh7994QPZmdXvndXGy3zaEy2AYLS-2Bn/pub


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Let's look at all the ways that they say you CAN NOT get "SARS-COV-2:"




"New evidence has emerged from China indicating that the LARGE MAJORITY OF CORONAVIRUS INFECTIONS DO NOT RESULT IN SYMPTOMS


"CORONAVIRUS" DISCOVERY Papers:

https://docs.google.com/document/d/e/2PACX-1vTCTJaZOpHk-OtFNIspUMha6AsXQVVSoEggOkpoCcFOmhyetd9JNUay4L_OWQR6QyeP7vGhE1L-Q7SN/pub

SARS-COV-1 PAPER:

https://docs.google.com/document/d/e/2PACX-1vTmbyriIRnfUglRxLyutnN5iHKHp8_6HAehnWUyVq1f6O9I96G05LppwJtEqiG1Sm5SfSFd8hiJGFVa/pub

ZAKI 2012 MERS CORONAVIRUS PAPER:

https://docs.google.com/document/d/e/2PACX-1vSI1S72a1aUGQYZDgjzci-pfV8hChKZTxjn13cJJ-ZReWGJTtNZa2xgbsvpqz3qND4VnbIvXZgD6iV5/pub

"SARS-COV-2" variants and mutations

https://docs.google.com/document/d/e/2PACX-1vSwugZCGN1YXfSp9uA6107GK7QEB4qRUWI1Dd4HK1ZeW0GfbKfxxzdXfmo4D8eRXIWTIVa3HGORqL1m/pub

PARK 2020 "SARS-COV-2" PAPER:

https://docs.google.com/document/u/1/d/e/2PACX-1vRDV1CzhDTOt1vcLXgOWTQbuU0xINS33Gw36XS01iZp0PeaPUpYaiBWcGNTght8tbRxg3XJ9WOagsL-/pub

ZHOU 2020 "SARS-COV-2" PAPER:

https://docs.google.com/document/u/1/d/e/2PACX-1vQLp23cndH32Xh5RILy7xVhkYF3YjGaNUbGKJGplkldyCApM5ViwzIQwniYq-OJo-YpbnU3pVq2rgFK/pub

ZHU 2020 "SARS-COV-2" PAPER:

https://docs.google.com/document/d/e/2PACX-1vRXgxa62Pae48hFM2_NS1F_aLWLoUzTRLqGSKEPchOgfXiwihqoUXsYiTIS7Jr3M75Itmkk5DXZ9qV0/pub

D.A TYRRELL 1965 "CORONAVIRUS" DISCOVERY:

https://docs.google.com/document/d/e/2PACX-1vTCTJaZOpHk-OtFNIspUMha6AsXQVVSoEggOkpoCcFOmhyetd9JNUay4L_OWQR6QyeP7vGhE1L-Q7SN/pub

CDC 2020 "SARS-COV-2" PAPER:

https://docs.google.com/document/d/e/2PACX-1vT0j2X9Di3-LvqnZ1RNRK9PyVr0-XUlz3NnWiWwesc5JpK5EriDhnSivpmOw0EM9iMLK9ST9JAYVEkh/pub

__________



FOUCHIER 2003 SARS-COV-1 KOCH'S POSTULATES FULFILLED(?):

https://docs.google.com/document/d/e/2PACX-1vSKgSmrotsg-xzD2KCgo1l7Y7AWeUt5f64Do8lO5xatzbNkVMPxobnZbs8pr0h9V8MkAmFPxTHdjBBo/pub

In order to prove a new pathogenic "virus" exists, Koch's Postulates must be satisfied first.

https://docs.google.com/document/d/e/2PACX-1vRBTuZK1288SKQhGnLnedB1wTvecFV7_BzwEWrOtlNhCUjBLqNEC6wXyaGX1BnGXK8tc5nwcDPZ67DF/pub

There is NO PROOF of a purified/isolated "Coronavirus" that fulfills Koch's Postulates:

https://docs.google.com/document/d/e/2PACX-1vSM71HNGOt63os_wsp_QRe9-E7F2uGASj--zr5zNW9HjNBxl8iC4sF1N6rmn_OAzugL_zROD4Eo26fZ/pub

DROSTEN 2020 "SARS-COV-2" PCR PAPER:

https://docs.google.com/document/d/e/2PACX-1vTQN9eziE3vTj2OZyiXS-Xcn6Qpj7NWzAvw4W_yBz5Bzrpmu2CzUFNLo40xV3vjJuPL3Bji-mVravRf/pub




__________

The Case against Rapid Mass Testing for "Coronavirus:"

https://docs.google.com/document/d/e/2PACX-1vRngCUUfZM6jouC6bdvDxOCbzVYRrH6FPfJpcIMCe8ooR5Llkq5dmsfCTd1OMM5HGfSucGjBJdgnrOE/pub

PCR Ct Value standard

https://docs.google.com/document/d/e/2PACX-1vSeBHVpoQs-ywbZNPORLby4NbreBkylH3ZQDqD-ZuKiXmMeTJWcK_7aFhqfW__j8nkietn_BNm1RKec/pub

Scathing review of the Drosten PCR test:

https://docs.google.com/document/d/e/2PACX-1vQZuDRP4aA5RaJ8kWaflLaB6f23iT5M59bqIfHNN334PnRFO453epe_dw5fpaoVDTr9R4i1oQ7xQsim/pub

Christian Drosten's history with fraud:

https://docs.google.com/document/d/e/2PACX-1vTLBAmMolLW8xG7dkOlR5cXG3Uh4l6E_M_YgMTxlxBZrQTYA9pTT8ARQalRC1rZ25NtxoXokaapUWuU/pub

Flu cases are being relabeled as "COVlD-19,"

https://docs.google.com/document/d/e/2PACX-1vSc_t_XbcnPhPCsMtiUvzhZIS7iaVIe9qz6VX7nAIL-_iMvhtMgNzoYvoqEavzDDpZaQNmKQyN_6e_3/pub


_____________

Two undeniable facts about "SARS-COV-2" (and any other "virus" for that matter):

https://docs.google.com/document/d/e/2PACX-1vTSc_Ciw5cB2quctJcKN4YRnk1oV74t-5nqTNBXHvRu5pVxHHtHpxngE0nWIbnCG6_ddCyEnTvOdePn/pub


______________________

THE HUMAN VIROME:

https://docs.google.com/document/d/e/2PACX-1vSpo40_wld8n1ZuVm5qUs_6yV4gQIVo9tHyzG3N3965BUnvXsIiKfmyWPEWOvYjCPQwxIhNDHknFWDL/pub

A huge problem for Virologists

https://docs.google.com/document/d/e/2PACX-1vRSC6Lu3VeC8zxHgt9ey0BD_8vncuW1YebFN25W-JDRrCpwohnmFTHNyniiZZ04jDwcoQ1Iqz8IXyNN/pub

MISINTERPRETING ELECTRON MICROSCOPE IMAGES:

https://docs.google.com/document/d/e/2PACX-1vRtNF-g18mgvOL45buaMhHJp-hfTvGLYf7SZe32m69zmnauOfr7hsr_hKUuo8642z_vf-b20RvStYaJ/pub

The vaccines have 95% efficacy...or 19%?

https://docs.google.com/document/d/e/2PACX-1vTNZmjZFzuFJAhxyWi3EyECQGJVXEKNk_Im3DdeQOqksyABV_nNHqj3wQYJGkG1xDAvc6eFYMP8OmV6/pub

"A Comparison of Plasmid DNA and mRNA as Vaccine Technologies" in April 2019:

https://docs.google.com/document/d/e/2PACX-1vSjGdAuz7ylrerc_9rtcA-sstCzHPrGn2Zrh0eG1ZWfoMsHvWeXQ9W3xR-D2uaSUmcUG41xQa-mFPWh/pub

Guidance An authorisation by the Chief Health Office under the s. 197 and s.198 Public Health Act 2016 (WA) to authorise relevant Australian Defence Force employees to supply and administer the COVID-19 Vaccine.

https://docs.google.com/document/d/e/2PACX-1vQ9PYzAZ-XQJvty9RSsNkkAgCoR3hmhVMmAEP7m5Y-jU6PUc7qJHn5cKkLEmzkssjGnVEYedp1xIEOx/pub

Beware those who would sell you on the disease and the "cure."

https://docs.google.com/document/d/e/2PACX-1vQnl8aBMGbDsNfRW1S9CH-s7bKatf9AQ_Ff9CvgqGpbiR_lcZ_zxf5tJdvDuSkvx6dUPJy5cfiJy9Ej/pub


____CASE AGAINST VIROLOGY___

Is complete purification/isolation of a "virus" even possible?

https://docs.google.com/document/d/e/2PACX-1vTx9BIQAwWZm7gi6v1_w9T_tWyknOEuRx8kCJVJ7tN_dcYUc8EwsF92AShh3HwmDOxLDVDd417jWjzO/pub

Purification of a "virus" is impossible

https://docs.google.com/document/d/e/2PACX-1vTjyUqE8tA2J7hdxTrmdgsa5o8EOR2DjAI08i52V6X_gAyHA6vMNas3dRwgm10FmYM12JKWeTrmyXUs/pub


THE CASE AGAINST CELL CULTURES:

https://docs.google.com/document/d/e/2PACX-1vTughyulJh5H2D5S5YxR4_DCXKI_3Yc-eTKWVaoK16z-3R5SWbW8DCoxhAn5YkeN_fEQzK1XHO0QzgX/pub

Cell line misidentification is a huge problem in cell cultures.

https://docs.google.com/document/d/e/2PACX-1vTrDRck0mqyo0X3wOVdLtubFXZYW200qnwo7AUZ0xpAvbAVG2ErTX1Y-TmOXhwKC3Go7ygsyiSOmMDC/pub

"Cell culture RELIES ON THE ASSUMPTION that the behavior of cells in vitro is fundamentally similar to their behavior as part of a tissue within an organ of a multicellular organism."

https://docs.google.com/document/d/e/2PACX-1vQzmhs4R7NkbxToUR1GyeLdF5iLZhgDkYkooiNFrg4HzielJu231losXzaWlPAxZFGmX-GJRnujhH0x/pub

Cell Cultures:

https://docs.google.com/document/d/e/2PACX-1vQfoMdQAMeYP0jJv6vHPPQtYleDrj1bsso67SQC3Q9iDHCjcoq1I_Yzj2vvbRaRTIUXHQjYD0HCLnoy/pub

SUB-CULTURING and CELL CULTURE ADAPTATIONS:

https://docs.google.com/document/d/e/2PACX-1vSmTM9raiDxVAp64o3yTdILEtWCuwmrhG7nb25YQbJKtuh2d2P9PMKOUD7Fv72Po-Ev3CJgKikiKEEr/pub

The Human Genome Is FULL OF VIRUSES

https://docs.google.com/document/d/e/2PACX-1vSPp3ZH2S_160J1HtvqStAMh19fuz2Me7AZacfn8RvpzIYxVPw_WL_4HdL_4xNYB2p9Y9BKu_opEJiU/pub

The Slippery Slope of Reference Genomics

https://docs.google.com/document/d/e/2PACX-1vQQTtEitoPXzw4X_sKVBsGe2JRRwntgcRLFW1HOuPINUTbZzJiWACW226A6oUJE8s5f2HRwhxj7bkaq/pub

VIRAL TRANSPORT MEDIA:

https://docs.google.com/document/d/e/2PACX-1vRIV5oXy0ZIFvSry6gJ09maJTqz1dJz_HTtzlZNfJYPB3k7vvrPrM2q3hT5F8r_zfv27rxqdTU2CiwZ/pub

The Case against Rapid Mass Testing for "Coronavirus:"

https://docs.google.com/document/d/e/2PACX-1vRngCUUfZM6jouC6bdvDxOCbzVYRrH6FPfJpcIMCe8ooR5Llkq5dmsfCTd1OMM5HGfSucGjBJdgnrOE/pub

PCR Ct Value standard

https://docs.google.com/document/d/e/2PACX-1vSeBHVpoQs-ywbZNPORLby4NbreBkylH3ZQDqD-ZuKiXmMeTJWcK_7aFhqfW__j8nkietn_BNm1RKec/pub

________________________


Mike Stones' FB page about viruses and antibodies

https://www.youtube.com/watch?v=jX_sq_z2q1w

https://www.facebook.com/mike.stone.54


_________________

ANTIBODY THEORY

_____________

PAUL EHRLICH'S 1900 SIDE-CHAIN THEORY (PART 1):

https://docs.google.com/document/d/e/2PACX-1vSWQ7pM49P09Qvdn1pj20KLoOCyX4Oyy5ShBJUWHGz5CQAqYrcLT4iGostVXFwA76qmKWp3ig2kh0uj/pub

PAUL EHRLICH'S 1900 SIDE-CHAIN THEORY PART 2: THE COMPLEMENT SYSTEM

https://docs.google.com/document/d/e/2PACX-1vSuc_MfqWttHYsJExUs9J0EIREKeAoPJQuGDtfUcsXMaWHtNaaSruZwMXZbX5hRRuHFQ3x8SHi2hib3/pub

RANK MACFARLANE BURNET 1957 CLONAL SELECTION THEORY:

https://docs.google.com/document/d/e/2PACX-1vRTYZcPSn95I6Bzv76jcNvpzNTbZpLp8iaIlnN1CuudmIpPU9D18ZUQxJjdt4i8zezs1lVgrSWuNPxV/pub

MICHAEL HEIDELBERGER 1929 ANTIBODY EQUATION:

https://docs.google.com/document/d/e/2PACX-1vRyx1BmVgSGgUnfw0WmRogR7hTp_OE4UBnv5M3jUO2rJfxlT-bZbDAwpBHLOJ2BW1HFtVRNF6P2GcN5/pub

LINUS PAULING'S 1940 ANTIBODY STRUCTURE THEORY:

https://docs.google.com/document/d/e/2PACX-1vS84ETojthpXnMKm3Jx7cUgJQ-89YjH7HTUxk2gTHVZRo8Rlkq_GNbTWS20Qw0LzrDYfunkG6kGUJd1/pub

ASTRID FAGRAEUS 1948 PLASMA CELLS PRODUCE ANTIBODIES CORRELATION:

https://docs.google.com/document/d/e/2PACX-1vQEsEGvTyyEniT90d-EM5iAofXcT0HohJUacWp6YSd00-7eDlhyrBjLgFInUGDqKAxY5u2kcvGUTEKc/pub

CHEMICAL STRUCTURE OF ANTIBODIES:

https://docs.google.com/document/d/e/2PACX-1vTQ29mU09Dxw7eD7jZaxD506033_dZPs2dowGjqwXR9gOybHeWQpGVtirkpHbdHvO7zWfY2ss6T88s_/pub

FIRST ATOMIC RESOLUTION STRUCTURE OF AN ANTIBODY FRAGMENT(?) 1973:

https://docs.google.com/document/d/e/2PACX-1vTEitvFbNZYKclrIuToydCxHONdMxK9x_SgPqM-xQ6Wady5R5WRK3KoJNJa9YdZvajQb7KVJhz2j5WF/pub

KÖHLER AND MILSTEIN'S 1975 MONOCLONAL ANTIBODIES:

https://docs.google.com/document/d/e/2PACX-1vT8pekwplFhqcCA65eKUQLkmvhb8BKw7c1CltZOncGHPRj2vnbcwSLpHLKu0Pi-aelfYcIsBKuTbAwm/pub

ANTIBODY IMAGES

https://docs.google.com/document/d/e/2PACX-1vSakKiCSr0b_7Kk35UUSy2GduDF9l3qQ-PyCSMjOMT_thSueSnUEN_gIVt0f_f1pzY3mSrvmXN3kPNw/pub

2011 TEM IMAGES OF ANTIBODIES(?):

https://docs.google.com/document/d/e/2PACX-1vQjtJIGaxef5vsmdLscy2FVs2IZF6cfZ8ohGfYV_GhbmioeSFjbqrM_0JvZB2qysc4Mo36O2xzkOU95/pub

MERRILL CHASE INADVERTENTLY DISPROVES ANTIBODIES IN 1942:

https://docs.google.com/document/d/e/2PACX-1vTAH850UMaXKRFBVIlng28qvCJIb6DqjbkZOEeHtSqHYn4f-udAX7nQx1IsWrNKFaBRJyE6u3D6cd8T/pub

DO ANTIBODIES EQUAL PROTECTION? THEY DON'T KNOW:

https://docs.google.com/document/d/e/2PACX-1vTb8BUHtDFpKVSX70xrHNSYoK9rmRSZE2pHUfwDQNEJeXHs6rivgnG8oKSb-V-5R8YsHgxzOp5SQbmQ/pub

REPRODUCIBILITY CRISIS IN ANTIBODY RESEARCH:

https://docs.google.com/document/d/e/2PACX-1vQKy0dFmzzadiL9EkG-mLfQE8UWds8sKfo5ykgxlov_OcNkc7H-9DAv35oc7ny9bAMH9RJfToAf5hBC/pub

ANTIBODIES ARE NOT REQUIRED FOR IMMUNITY:

https://docs.google.com/document/d/e/2PACX-1vQ2ipqUmdXnH_5gRwwPuUSxxzHx8MJrvvMyWx-AUpOg5acEx3rDlt9QNJUI5DmKA6biMCa8ciuHpnu-/pub

ACP's NEW "COVID-19" ANTIBODY GUIDELINES:

https://docs.google.com/document/d/e/2PACX-1vQw80KVLxFxRyLtgAM8XqYRfBQWkgYp1poOftiwgz8KyAbjLTtR8GhsNxbgNzQSyre7_g4iSCOxghOo/pub

ANTIBODY MADNESS! MISSING ANTIBODY, MISSING PROTECTION?:

https://docs.google.com/document/d/e/2PACX-1vThXfZwg1Os5HEfIZE_ThkUohR_I-t4AnhBlCC9Dct6vOzVb8v38IW0KSvQ5tHOwp1lALKwWTLtrrA0/pub

ANTIBODY SPECIFICITY?:

https://docs.google.com/document/d/e/2PACX-1vQbMvfH_zyuzbOFynD1PFEAdLYVCStkXeVld8PxJ6K0U7i2FMZ4hAx0qgdB2VITeTQeyAaKeeVR0YOM/pub




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ONE OF MANY FOI

https://www.fluoridefreepeel.ca/fois-reveal-that-health-science-institutions-around-the-world-have-no-record-of-sars-cov-2-isolation-purification/?fbclid=IwAR0Zvup0CY7zklhX0YEZWKckGk-tr5geG4a-KPxqeviL6LvkADYOATQDM_I


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MY OWN WITH HELP INVESTIGATION INTO CLAIMS OF A PURIFIED ISOLATED SARSCOV2 "VIRUS"

(A BOUT WITH YOUTUBER CALIMING TO DEBUNK THE VIROLOGY DEBUNKERS)

There seems to be a number of loose ends from this paper.1. They state that their specimen was "SARS-CoV-2 (isolate MUC-1, kind gift of G. Dobler..." - where did G. Dobler get the sample from and how had it been prepared to this stage? i.e. how do we know it's a virus per se. 2. They describe a virus "purification" process with "infected" Vero cells but don't seem to show any evidence at the end of the process that they had achieved purification e.g. comparison of electron micrographs. 3. After their "purification" they report they had a "...limited amount of available RNA" - that's not promising! Then they start their sequencing... Perhaps all we can say is that the authors performed some very technical experiments on particles that were not purified and not shown to be a virus. To be fair to these authors it doesn't look like they were claiming to have isolated and purified SARS-CoV-2 even through the word purify appeared in the paper.

(FROM THE MATERIALS SECTION OF THAT PAPER)

"Materials and Methods

SARS-CoV-2 propagation

SARS-CoV-2 (isolate MUC-1, kind gift of G. Dobler, Bundeswehr Institute for

Microbiology) was used for cell infections. It was propagated on Vero E6 cells (ATCC®

CRL-1586) with an adsorption of 1 h at 37°C and shaking every 10-15 min. "

https://science.sciencemag.org/.../abd5223_Turonova_SM.pdf https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7665311/


They state they were gifted an "isolate" which does not say where it came from or what was done to it. The fact that they cultured the "virus" in Vero cells tells you everything you need to know as to whether it is purified or not. Basically the same old cell culture junk with limited information on the actual specimen:

"SARS-CoV-2 (isolate MUC-1, kind gift of G. Dobler, Bundeswehr Institute for Microbiology) was used for cell infections. It was propagated on Vero E6 cells....

... (ATCC® CRL-1586) with an adsorption of 1 h at 37°C and shaking every 10-15 min. Infected cells were controlled for cytopathic effect every 24h and culture supernatant was usually

collected 48h-72h post infection,"


On top of that, they can not claim "SARS-COV-2" was finally purified/isolated in Oct. 2020. It would have had to have been purified/isolated at the time of the original publications in January 2020 when they supposedly got the sequence and EM images. You can't state it wasn't done back then but was in Oct. That is ridiculous.

Even if this paper was proof of a purified/isolated "SARS-COV-2" (it isn't) they would still need to prove it pathogenic which to date has yet to be done as no suitable animal model which accurately recreates the human disease exists at all.

__________


If a "virus" exists, it should be able to be taken and purified/isolated directly from the sick patient. If they can't do that, how did they ever determine "viruses" existed and needed to be cultured in the first place? They create particles through cell culturing and claim them as "viruses" because these particles can not be found when taken from sick humans.

What evidence shows "viruses" must be cultured? If they state there is too little "virus" in the sample from a sick patient, where was this determined? They would still need purified/isolated particles directly from a sick patient first in order to determine there is not enough and that cell culturing is the best way to produce more. However, they never did that.

________________________


“The researchers claim they decided which is the real genome of SARS-CoV-2 by “consensus,” sort of like a vote. Again, different computer programs will come up with different versions of the imaginary “unicorn,” so they come together as a group and decide which is the real imaginary unicorn.”


#2 COVID Admission: CDC Scientists Found That SARS-CoV-2 Didn’t Infect Human Tissue

A big part of the official story we were told was that COVID was a new, dangerous and unpredictable disease that was both fast-spreading and lethal. Well, it’s apparently not very lethal since the CDC scientists found that it couldn’t even infect human cells in vitro.

https://luis46pr.wordpress.com/2020/11/02/study-cdc-scientists-make-2-covid-admissions-that-destroy-official-narrative/?fbclid=IwAR24avbVYDpJ3ntn73qp9NnNUw0mePSJf-rhA2WxBZzYDPg8jiDXqDwn9Oc



Now from here WE should segway into what can PCR actually detect ....

From a fellow investigator;

PCR is testing ACE2/TMPRSS2 expression, which is caused by Radiation. Yes, it's meaningless for "virus" infection, but if you think about "Radiation Injury" it's not that meaningless.


HALF OF MY BLOGS ARE COLLECTION FROM OTHERS FINDINGS

https://nateserg808.wixsite.com/my-site/post/fly-ball-catch

https://nateserg808.wixsite.com/my-site/post/fly-ball-catch-2

https://nateserg808.wixsite.com/my-site/post/a-new-take-on-denim

https://nateserg808.wixsite.com/my-site/post/magic-shows

https://nateserg808.wixsite.com/my-site/post/timeless-summer-items-every-closet-must-have


______________________________



________________________________________________

SO WHATS CAUSING ILLNESS IF NOT A "VIRUS"??



__________________

Evidence for a Connection Between COVID-19 and Exposure to Radiofrequency Radiation from Wireless Telecommunications Including Microwaves and Millimeter Waves

https://osf.io/9p8qu/ (Published Med Lit link)

(Article on Publication)

Evidence for a Connection between COVID-19 and Exposure to Radiofrequency Radiation from Wireless

Telecommunications Including Microwaves and Millimeter Waves

Beverly Rubik and Robert R. Brown

_ COVID-19 public health policy has focused on the SARS-CoV-2

virus and its effects on human health while environmental factors have been

largely ignored. In considering the epidemiological triad (agent-host environment) applicable to all disease, we investigated a possible

environmental factor in the COVID-19 pandemic: ambient radiofrequency

radiation from wireless communication systems including microwaves and

millimeter waves. COVID-19 surfaced in Wuhan, China shortly after the

implementation of city-wide 5G (fifth generation of wireless radiation), and

spread globally, demonstrating a statistical correlation to international

communities with 5G antennas installed. In this study, we examined the peer reviewed scientific literature on the detrimental bioeffects of radiofrequency

radiation (RFR) and identified several ways in which RFR may be

contributing to COVID-19 as a toxic environmental cofactor. We conclude

that RFR and, in particular, 5G, which involves 4G infrastructure

densification, has exacerbated COVID-19 prevalence and severity by

weakening host immunity and increasing SARS-CoV-2 virulence by (1)

causing morphologic changes in erythrocytes including echinocyte and

rouleaux formation that may be contributing to hypercoagulation; (2)

impairing microcirculation and reducing erythrocyte and hemoglobin levels

exacerbating hypoxia; (3) amplifying immune system dysfunction, including

immunosuppression, autoimmunity, and hyperinflammation; (4) increasing

cellular oxidative stress and the production of free radicals exacerbating

vascular injury and organ damage; (5) augmenting intracellular Ca2+ essential

for viral entry, replication, and release, in addition to promoting pro inflammatory pathways; and (6) worsening heart arrhythmias and cardiac

disorders. In short, RFR is a ubiquitous environmental stressor that

contributes to adverse health outcomes of COVID-19. We invoke the

Precautionary Principle and strongly recommend a moratorium on 5G

wireless infrastructure at this crucial time to help mitigate the pandemic, and

to preserve public health until governmental safety standards for RFR

exposure based on current and future research are defined and employed.

https://zero5g.com/wp-content/uploads/2021/03/Rubik-Brown-COVID-19-and-RFR-SUBMITTED.pdf


Commonalities Between COVID-19 and Radiation Injury

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861125/?fbclid=IwAR2QKp1H_GJKAKlV71MyWKJ15QONNL3hGZTwSjmY4obQ1EbKFlD4EJlWJuU

" As the multi-systemic components of COVID-19 emerge, parallel etiologies can be drawn between SARS-CoV-2 infection and radiation injuries. While some SARS-CoV-2-infected individuals present as asymptomatic, others exhibit mild symptoms that may include fever, cough, chills, and unusual symptoms like loss of taste and smell and reddening in the extremities (e.g., “COVID toes,” suggestive of microvessel damage). Still others alarm healthcare providers with extreme and rapid onset of high-risk indicators of mortality that include acute respiratory distress syndrome (ARDS), multi-organ hypercoagulation, hypoxia and cardiovascular damage. Researchers are quickly refocusing their science to address this enigmatic virus that seems to unveil itself in new ways without discrimination. As investigators begin to identify early markers of disease, identification of common threads with other pathologies may provide some clues. Interestingly, years of research in the field of radiation biology documents the complex multi-organ nature of another disease state that occurs after exposure to high doses of radiation: the acute radiation syndrome (ARS). Inflammation is a key common player in COVID-19 and ARS, and drives the multi-system damage that dramatically alters biological homeostasis. Both conditions initiate a cytokine storm, with similar pro-inflammatory molecules increased and other anti-inflammatory molecules decreased. These changes manifest in a variety of ways, with a demonstrably higher health impact in patients having underlying medical conditions. The potentially dramatic human impact of ARS has guided the science that has identified many biomarkers of radiation exposure,..."


"... Here we highlight some of the systems and immunological areas affected by both COVID-19 and acute radiation exposure, albeit to different levels. In both cases, the result is a systemic insult that can cause damage to many parts of the body, including the vascular system, lung, heart, kidneys, liver, gut, eyes and brain. Regardless of the target organ, the hyperactivation of the immunogenic pathways are at the heart of the body’s response to overcome SARS-CoV-2 and acute radiation exposure (1). Cytokines are produced by a variety of immune cells (i.e., macrophages, B lymphocytes, T lymphocytes and mast) and non-immune cells (i.e., endothelial, fibroblasts and stromal). Under normal circumstances, cytokines have a short half-life and act as local mediators within a microenvironment; therefore, circulating cytokines in the blood are below the limit of detection of most commercially available assay kits (2). This complex communication network provides a healthy immune system with the proper signals to mount a proportionate response against an infectious agent or inflammatory stimuli. In other cases, the reaction is so strong that circulating cytokine levels surge, resulting in a “cytokine storm” (also called hypercytokinemia3) or an overaction of the immune system creating a generalized inflammatory response that can lead to systemic tissue damage. The cytokine storm is the nexus between SARS-CoV-2 infection and radiation exposure; both result in systemic inflammation that ravages the body (1, 3).

A wealth of early literature has described the cytokine storm syndrome (CSS) in COVID-19 patients (4–15). For example, in a study of 50 patients, expression levels of 14 of 48 cytokines studied were associated with disease severity and progression, with interferon (IFN)-γ-induced protein 10 and monocyte chemotactic protein-3 noted as excellent predictors of disease progression (16). Increases in granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin-6 (IL-6) due to T-cell overactivation were also noted (17). Another retrospective study with 3,939 patients shows both mild and severe forms of COVID-19 disease resulting in changes in circulating leukocyte subsets and cytokine secretion (8). In particular, Vaninov et al. noted that persistent high levels of three cytokines (CXCL10, CCL7 and IL-1 receptor antagonist) were associated with increased viral load, loss of lung function, lung injury and a fatal outcome (12). Based on these kinds of findings of elevated levels of specific cytokines, in June 2020 the FDA issued an Emergency Use Authorization (EUA) for an in vitro diagnostic test based on measuring the circulating IL-6 levels in serum or plasma for the management of patients with COVID-194 (discussed in more detail below). However, emerging technologies measuring “cytokine signatures” demonstrate variability across subjects and highlight the need for the development of personalized treatments based on these data.

As observed with COVID-19, cytokines are also released by many cells after radiation exposure, including endothelial cells, fibroblasts, immune cells and parenchymal cells. The interplay and early activation of inflammatory reactions involving proteins in cytokine cascade, such as fibroblast growth factor (FGF), transforming growth factor (TGF), tumor necrosis factor (TNF-α), and interleukins (ILs) is thought to be responsible for DEARE. Cytokines and chemokines that attract immune cells and lead to inflammation include IL-1α and IL-6. Inflammatory cells cause numerous other changes to occur, such as cell death, promotion of fibrosis and swelling of the tissue. These cytokines are involved in both early and late reactions, like the major cytokines in the response of skin cells to ionizing radiation, and include IL-1, IL-6, tumor necrosis factor (TNF)-α, transforming growth factor (TGF)-β, which can be pro-or anti-inflammatory depending on the tissue and context of release, and the chemokines...."

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861125/?fbclid=IwAR2QKp1H_GJKAKlV71MyWKJ15QONNL3hGZTwSjmY4obQ1EbKFlD4EJlWJuU


______________________________

Dr. Martin Pall has discovered the mechanism of how Electro Magnetic Field affecting our body biologically. He explained that when EMF hits our body, it activates Calcium Channel and opens it up, and then it allows excess amount of Calcium flow into the cells. that increases the calmodulin dependent Nitric Oxide, that causes hypoxia eventually, this calmodulin interacts with ACE2, it is responsible of shedding ACE2.

So I found this study about CoVid from my file, and read it again....

They suggest to use existing drugs such asclude recombinant soluble ACE2, indirect ACE2 modulators (angiotensin receptor blockers, calmodulin antagonists, selective oestrogen receptor modifiers), TMPRSS2 inhibitors (camostat mesylate, nafamostat mesylate, antiandrogens, inhaled corticosteroids) and ADAM-17 enhancers (5-fluorouracil).

Yeah, they say, ACE2 and Calmodulin.....Coincidence, right?

https://www.youtube.com/watch?v=vTGJQqV8QGc


PCR is testing ACE2/TMPRSS2 expression, which is caused by Radiation. Yes, it's meaningless for "virus" infection, but if you think about "Radiation Injury" it's not that meaningless.

"Inhibition of SARS-CoV-2 entry through the ACE2/TMPRSS2 pathway..."

https://pubmed.ncbi.nlm.nih.gov/32696234/


Scientific evidence contradicts findings and assumptions of Canadian Safety Panel 6: microwaves act through voltage-gated calcium channel activation to induce biological impacts at non-thermal levels, supporting a paradigm shift for microwave/lower frequency electromagnetic field action

https://pubmed.ncbi.nlm.nih.gov/25879308/


EMFs open the calcium channels, causing calcium influx into the cell. This is researched by Dr. Martin Pall1, who showed that the calcium channels in each of your cells stay open because they get disrupted by microwave radiation.

https://drpompa.com/cellular-detox/emf-toxins/#:~:text=EMFs%20open%20the%20calcium%20channels%2C%20causing%20calcium%20influx,of%20calcium%20ions%20are%20allowed%20to%20flow%20in


Electromagnetic fields act via activation of voltage-gated calcium channels to produce beneficial or adverse effects Martin L. Pall *

Professor Emeritus of Biochemistry and Basic Medical Sciences, Washington State University, Portland, OR, USA

https://www.emfanalysis.com/wp-content/uploads/2015/06/EMF-Effects-via-Voltage-Gated-Calcium-Channels-Dr-Martin-Pall.pdf


Calmodulin interacts with angiotensin-converting enzyme-2 (ACE2) and inhibits shedding of its ectodomain

https://pubmed.ncbi.nlm.nih.gov/18070603/

https://www.sciencedirect.com/science/article/pii/S0014579307012392


(newest) Calmodulin Mediates DNA Repair Pathways Involving H2AX in Response to Low-Dose Radiation Exposure of RAW 264.7 Macrophages

https://pubs.acs.org/doi/10.1021/tx800236r?fbclid=IwAR08BUYj5Fe7ytGbtFH5nCZ3d-ow9LKeyCAVKtZAZVuAAkhEtkWJf-ALeyE


Think Outside the Virus ~ VGCC and Calcium Channel Blocker ~ Coincidence #2

Mari Kashiwagi

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

REFERENCES:

Voltage-Gated Calcium Channels

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140680/

Dr Martin Pall Interview (long) Navy's Electromagnetic Emitters and Health Effects

https://youtu.be/pLRgZza8PXg

Dr. Matt & Dr. Mike - ACE Inhibitor

https://youtu.be/jJvZFi6UyOc

Mechanism of Action of ACE inhibitors

https://youtu.be/jJvZFi6UyOc

Repurposing calcium channel blockers as antiviral drugs

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438026/

Low serum calcium: a new, important indicator of COVID-19 patients from mild/moderate to severe/critical

https://portlandpress.com/bioscirep/article/40/12/BSR20202690/227080/Low-serum-calcium-a-new-important-indicator-of

Calmodulin interacts with angiotensin‐converting enzyme‐2 (ACE2) and inhibits shedding of its ectodomain

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094239/

SARS-CoV-2, Hypoxia, and Calcium Signaling: The Consequences and Therapeutic Options

https://pubs.acs.org/doi/10.1021/acsptsci.0c00219

How Electromagnetic Fields (EMFs) Effect Biology Via Voltage-Gated Calcium Channels (VGCC) Activation

https://thebridgelifeinthemix.info/technology/electromagnetic-fields-emfs-affect-biology/

New Research Suggests Magnesium and Vitamin D Can Help Reduce COVID-19 Infections

https://www.saintlukeskc.org/about/news/new-research-suggests-magnesium-and-vitamin-d-can-help-reduce-covid-19-infections

Inhibition of SARS-CoV-2 entry through the ACE2/TMPRSS2 pathway: a promising approach for uncovering early COVID-19 drug therapies

ACE inhibition attenuates radiation-induced cardiopulmonary damage https://link.springer.com/article/10.1007/s00228-020-02963-4

Treating Hypertension with Calcium Channel Blockers

https://www.healthline.com/health/heart-disease/calcium-channel-blockers#natural-ccbs

ACE inhibition attenuates radiation-induced cardiopulmonary damage

https://www.sciencedirect.com/science/article/pii/S0167814014004964

Coronary Calcium in COVID-19 Patients Linked to Worse Outcomes

https://www.tctmd.com/news/coronary-calcium-covid-19-patients-linked-worse-outcomes

________________________

5G Risk:

The Scientifc Perspective

Compelling Evidence for Eight Distinct Types

of Great Harm Caused by Electromagnetic

Field (EMF) Exposures and the

Mechanism that Causes Them

Written and Compiled by

Martin L. Pall, PhD

Professor Emeritus of Biochemistry and Basic Medical Sciences

Washington State University

BA degree in Physics, Phi Beta Kappa, with honors, Johns Hopkins University;

PhD in Biochemistry & Genetics, Caltech.

martin_pall@wsu.edu

503-232-38835GCRISIS the5Gsummit.com 3

Chapter 1 < Pg 8 Eight Extremely Well-Documented Effects of

Non-Thermal EMF Exposures: Role of

Pulsations, Other Factors that Infuence EMF

Effects

Chapter 2 < Pg 24 How Each Such EMF Effect Is Directly Produced

via Voltage-Gated Calcium Channel Activation:

Role of the Voltage Sensor in Producing the

Extraordinary Sensitivity to EMF Effects

Chapter 3 < Pg 32 Strong Evidence for Cumulative and Irreversible

EMF Effects

Chapter 4 < Pg 39 EMFs Including Wi-Fi May Be Particularly

Damaging to Young People

Chapter 5 < Pg 41 The Importance of the SCENIHR 2015

Documentand the Many Omissions, Flaws and

Falsehoods in That Document

Chapter 6 < Pg 84 The U.S. Early Role in Recognizing Non-Thermal

EMF Effects and How This Was Abandoned

Starting in 1986: U.S. Failure to Research

Health Impacts of Cell Phone Towers, Cell

Phones, Wi-Fi, Smart Meters and Now 5G.

What Is the Current Position of U.S.

Government Agencies?

Chapter 7 < Pg 113 The Great Risks of 5G: What We Know and

What We Don’t Know

CONTENTS5GCRISIS the5Gsummit.com 4

SUMMARY

We know that there is a massive literature,

providing a high level of scientifc certainty,

for each of eight pathophysiological effects

caused by non-thermal microwave frequency

EMF exposures. This is shown in from 12 to 35

reviews on each specifc effect, with each review

listed in Chapter 1, providing a substantial body

of evidence on the existence of each effect.

Such EMFs:

1. Attack our nervous systems including our brains leading to widespread neurological/

neuropsychiatric effects and possibly many other effects. This nervous system attack

is of great concern.

2. Attack our endocrine (that is hormonal) systems. In this context, the main things that

make us functionally different from single celled creatures are our nervous system and

our endocrine systems – even a simple planaria worm needs both of these. Thus the

consequences of the disruption of these two regulatory systems is immense, such that

it is a travesty to ignore these fndings.

3. Produce oxidative stress and free radical damage, which have central roles in

essentially all chronic diseases.

4. Attack the DNA of our cells, producing single strand and double strand breaks in

cellular DNA and oxidized bases in our cellular DNA. These in turn produce cancer and

also mutations in germ line cells which produce mutations in future generations.

5. Produce elevated levels of apoptosis (programmed cell death), events especially

important in causing both neurodegenerative diseases and infertility.

6. Lower male and female fertility, lower sex hormones, lower libido and increased levels

of spontaneous abortion and, as already stated, attack the DNA in sperm cells.

7. Produce excessive intracellular calcium [Ca2+]i and excessive calcium signaling.

8. Attack the cells of our bodies to cause cancer. Such attacks are thought to act via

15 different mechanisms during cancer causation.

There is also a substantial literature showing that EMFs also cause other effects including

life threatening cardiac effects (Chapter 3). In addition substantial evidence suggests EMF

causation of very early onset dementias, including Alzheimer’s, digital and other types

of dementias (Chapter 3); and there is evidence that EMF exposures in utero and shortly

after birth can cause ADHD and autism (Chapter 5).5GCRISIS the5Gsummit.com 5

Each of these effects is produced via the main mechanism of action of microwave/lower

frequency EMFs, activation of voltage-gated calcium channels (VGCCs) (Chapter 2). Each

of them is produced via what are called downstream effects of VGCC activation.

It follows from this that we have a good understanding not only that these effects occur,

but also how they can occur. The extraordinary sensitivity of the VGCC voltage sensor

to the forces of the EMFs tells us that the current safety guidelines allow us to be

exposed to EMF levels that are something like 7.2 million times too high. That sensitivity

is predicted by the physics. Therefore, the physics and the biology are each pointing to

the same mechanism of action of non-thermal EMFs.

The different effects produced are obviously very deep concerns. They become much

deeper and become existential threats when one considers that several of these effects

are both cumulative and eventually irreversible. There is substantial evidence for the

cumulative nature and eventual irreversibility of the neurological/neuropsychiatric

effects, of the reproductive effects, the mutational DNA effects, the cardiac effects, of

some but not other of the hormonal effects (Chapter 3); any causation of ADHD and

autism may add additional concerns (here the cumulative nature is probably limited

to the perinatal period). When we know that sperm counts have dropped by more

than 50% throughout the technologically advanced countries on earth, it is diffcult

to avoid the conclusion that the vast majority of the population in those countries

is already substantially impacted. The same conclusion can be made based on the

widespread nature of the neuropsychiatric effects in those countries. Both of those

effects will get much much worse even with no increase in current exposures, due to

the cumulative nature and irreversibility of these effects. I expect we will see crash in

human reproduction almost to zero as happened in the Magras and Xenos mouse study

which I estimate to occur within about 5 years, without any increases in our exposures.

Obviously 4G and 5G will make the situation much worse. Similarly I expect that the

deterioration in brain function that we are already seeing will seal our fate if we fail

to act rapidly and vigorously. Our collective brain function may become completely

incapable of dealing with such a mega-crisis situation.

Now it can be argued that some of these may not develop as I expect, although those

expectations are based on the best available evidence. One may even be able to argue

this for all of those expectations. However, when we have substantial risk of multiple

existential threats to every single technologically advanced country on earth, failure

to act vigorously means there is a very high probability of complete destruction of

these societies. And the chaos which would inevitably ensue, in a world that still has

nuclear weapons, may well lead to extinction. In the face of these types or risk, the only

reasonable course is to move with great vigor to stop new exposures and lower current

exposures. One can still access the internet, using wired connections. And we can lower 5GCRISIS the5Gsummit.com 6

cell phone tower and cell phone radiation substantially. Smart meters, if needed, can

work via wired connections.

Over 60% of this document (Chapters 5 & 6), is focused on the failures of statements

from SCENIHR, the telecommunications industry, the U.S. FCC and the U.S. FDA to

refect the science. Their statements repeatedly omit much, often all of the most

important science. Their statements are rife not only with omissions, but also with

easily demonstrable falsehoods and with false logic. These have often occurred at

times where we know that they knew better. These have occurred along with vigorous

efforts by the telecommunications industry to corrupt the science by attacking individual

scientists whose only fault is that they have obtained important findings that the

industry does not like. These attacks have occurred along with vigorous efforts to

corrupt two agencies that have important regulatory roles.

There are also possible concerns about individual industry-linked research studies.

All wireless communication devices put out polarized EMFs that carry information via

pulsations. Both the pulsations and the polarization make these EMFs much more

biologically active. There are three other factors that also infuence the production of

effects. Several industry-linked studies may have used these factors, along with using

very tiny numbers of individual animals in their studies, to produce studies which may

have been designed to fail (Chapter 5). It is not clear at this point whether this type of

concern is quite limited or whether it is very broad.

The European Commission has done nothing to protect European citizens from any of

these very serious health hazards and the U.S. FDA, EPA and National Cancer Institute

have done nothing to protect American citizens. The U.S. FCC has been much worse

than that, acting vigorously with wanton disregard for our health.







ABSTRACT This monograph describes the largest unethical medical experiment in human history: the implementation and operation of non-ionizing non-visible EMF radiation (hereafter called wireless radiation) infrastructure for communications, surveillance, weaponry, and other applications. It is unethical because it violates the key ethical medical experiment requirement for “informed consent” by the overwhelming majority of the participants. The monograph provides background on unethical medical research/experimentation, and frames the implementation of wireless radiation within that context. The monograph then identifies a wide spectrum of adverse effects of wireless radiation as reported in the premier biomedical literature for over seven decades. Even though many of these reported adverse effects are extremely severe, the true extent of their severity has been grossly underestimated. Most of the reported laboratory experiments that produced these effects are not reflective of the real-life environment in which wireless radiation operates. Many experiments do not include pulsing and modulation of the carrier signal, and most do not account for synergistic effects of other toxic stimuli acting in concert with the wireless radiation. These two additions greatly exacerbate the severity of the adverse effects from wireless radiation, and their neglect in current (and past) experimentation results in substantial under-estimation of the breadth and severity of adverse effects to be expected in a real-life situation. This lack of credible safety testing, combined with depriving the public of the opportunity to provide informed consent, contextualizes the wireless radiation infrastructure operation as an unethical medical experiment.


https://smartech.gatech.edu/bitstream/handle/1853/62452/LARGEST_UNETHICAL_MEDICAL_EXPERIMENT_FINAL.pdf?sequence=4&isAllowed=y&fbclid=IwAR2IRNq6hjgOHlErCIb2kO2d2Mag-vowmxSlcxo-xFttihYdI5oiwiyn6po




____________________ 60GHZ _________________________

The 5G system is a WiGig wireless network that operates in the 60GHz spectrum with a download speeds of up to 10 Gbps compared to the 4G download speed of 10 Mbps.

However, the frequency of 60 GHz is the frequency at which oxygen molecules oscillate. At 60 GHz, 98% of the transmitted 5G energy will be absorbed by atmospheric oxygen which then alters the orbital properties of the electrons of the oxygen molecules. '"60GHz is the frequency of oxygen molecule absorption. Oxygen molecules have electrons that they share with each other, oxygen is a diatomic molecule. What we breathe are two oxygen molecules bonded together with the electrons that they share.” When the oxygen molecule is hit with 60GHz 5G waves, these waves affect the orbital resonance properties of those shared electrons. It is those shared electrons that bind to the hemoglobin in our blood.' When the oxygen is disrupted, it will no longer bind to the hemoglobin and myoglobin (oxygen carrying molecules) and therefore will not be able to carry oxygen to the cell's powerhouse 'mitochondria'. Without oxygen, the liver becomes congested and the body, and brain, begins to break down due to slow suffocation.

Because the brain is the body organ most sensitive to the lack of oxygen, not getting enough oxygen to the brain will result in brain hypoxia. Brain hypoxia symptoms range from mild to severe.

Mild symptoms include:

cognitive disturbances / temporary memory loss / reduced ability to move your body / difficulty paying attention / difficulty making sound decisions / Severe symptoms include:

fainting / seizure / coma / brain death

Note: What do 5G and masks have in common, they both lead to oxygen deprivation!

The masks play another role in restricting your breathing ability. You can't pull normal amount of air to fill your entire lungs. So you end up getting less oxygen because you're getting less air.

Note: The spectrum for 4G starts from 700 MHz to 5 GHz frequency bands. "Compared to the frequencies below 5 GHz previously used by mobile devices, millimeter wave technology allows transmission on frequencies between 30 GHz and 300 GHz. These frequencies are called millimeter waves because they have wavelengths between 1 mm and 10 mm, while the wavelengths of the radio waves currently used by smartphones are mostly several dozen centimeters."

Note: Health Effects of cumulative low intensity Radio Frequency radiation exposure include:

DNA mutations

Mitochondrial damage

Tumors, cancer (children’s skulls receive more radiation)

Heart palpitations / Memory and cognitive problems / Sperm changes and infertility / Headaches, migraines, ringing of ears / ADHD / Anxiety / Depression / Heart Disease / Type-2 Diabetes

Radiofrequency/microwave (RF/MW) radiation affect the Schumann Resonance signals which are the mechanism through which melatonin production is activated.

Note: The frequencies also affect the bodies ability to produce Vitamin D (Vitamin D deficiency causes cold and flu due to the weakening of the immune system. This is the reason why people are prone to cold and flu in the winter season).

Note: The electromagnetic radiation in the microwave frequency range 'are absorbed by water, fats, sugars, and certain other molecules, whose consequent vibrations produce *heat*.' Similar to microwave ovens which generate radiation at a frequency of about 2.45GHz (the microwave energy is converted to thermal energy by causing water molecules to flip back and forth some 2.45 billion times a second...The 60 GHz used by the 5G system causes water molecules to flip back and forth 60 billion times a second!!!)

Note: Main symptoms of Coronavirus: Shortness of breath, Coughing, Fever. They have also shown how people suddenly fall down with seizures which are the same symptoms caused by severe brain hypoxia." - Jeffrey James Luckay

______________

The claim is that microwave radiation from cellphones and wi-fi is emitted at levels too low to cause biological effects.

That claim has been proven to be false (as is more than adequately shown in the attached link). Of course many have a vested interest in keeping that information from being widely-known (this is also covered in the attached link).

________


5G: Great risk for EU, U.S. and International Health! Compelling Evidence for Eight Distinct Types of Great Harm Caused by Electromagnetic Field - (EMF) Exposures and the Mechanism that Causes Them

https://peaceinspace.blogs.com/files/5g-emf-hazards--dr-martin-l.-pall--eu-emf2018-6-11us3.pdf?fbclid=IwAR37AzUXHXvj5r0cZWxTsHJXgs_T3RnToJu8_2-pDEqlxZe2oWzgUzA1XAQ


Large Resource on EMF Damages

https://envirowatchrangitikei.wordpress.com/2020/08/09/a-closer-look-at-the-live-training-simulation-exercise-under-who-that-preceded-the-plandemic-in-october-2019/?fbclid=IwAR0AxncLoCFAfpdMaYbwwId9IEd07AziM28qEH9AZEWI5q7pSawTQqJgEgM


Millimeter (MM) wave and microwave frequency radiation produce deeply penetrating effects: the biology and the physics

https://pubmed.ncbi.nlm.nih.gov/34043892/




5G Risk:

The Scientifc Perspective

Compelling Evidence for Eight Distinct Types

of Great Harm Caused by Electromagnetic

Field (EMF) Exposures and the

Mechanism that Causes Them

Written and Compiled by

Martin L. Pall, PhD

Professor Emeritus of Biochemistry and Basic Medical Sciences

Washington State University

BA degree in Physics, Phi Beta Kappa, with honors, Johns Hopkins University;

PhD in Biochemistry & Genetics, Caltech.

SUMMARY

We know that there is a massive literature,

providing a high level of scientifc certainty,

for each of eight pathophysiological effects

caused by non-thermal microwave frequency

EMF exposures. This is shown in from 12 to 35

reviews on each specifc effect, with each review

listed in Chapter 1, providing a substantial body

of evidence on the existence of each effect.

Such EMFs:

1. Attack our nervous systems including our brains leading to widespread neurological/

neuropsychiatric effects and possibly many other effects. This nervous system attack

is of great concern.

2. Attack our endocrine (that is hormonal) systems. In this context, the main things that

make us functionally different from single celled creatures are our nervous system and

our endocrine systems – even a simple planaria worm needs both of these. Thus the

consequences of the disruption of these two regulatory systems is immense, such that

it is a travesty to ignore these fndings.

3. Produce oxidative stress and free radical damage, which have central roles in

essentially all chronic diseases.

4. Attack the DNA of our cells, producing single strand and double strand breaks in

cellular DNA and oxidized bases in our cellular DNA. These in turn produce cancer and

also mutations in germ line cells which produce mutations in future generations.

5. Produce elevated levels of apoptosis (programmed cell death), events especially

important in causing both neurodegenerative diseases and infertility.

6. Lower male and female fertility, lower sex hormones, lower libido and increased levels

of spontaneous abortion and, as already stated, attack the DNA in sperm cells.

7. Produce excessive intracellular calcium [Ca2+]i and excessive calcium signaling.

8. Attack the cells of our bodies to cause cancer. Such attacks are thought to act via

15 different mechanisms during cancer causation.

There is also a substantial literature showing that EMFs also cause other effects including

life threatening cardiac effects (Chapter 3). In addition substantial evidence suggests EMF

causation of very early onset dementias, including Alzheimer’s, digital and other types

of dementias (Chapter 3); and there is evidence that EMF exposures in utero and shortly

after birth can cause ADHD and autism (Chapter 5).5GCRISIS the5Gsummit.com 5

Each of these effects is produced via the main mechanism of action of microwave/lower

frequency EMFs, activation of voltage-gated calcium channels (VGCCs) (Chapter 2). Each

of them is produced via what are called downstream effects of VGCC activation.

It follows from this that we have a good understanding not only that these effects occur,

but also how they can occur. The extraordinary sensitivity of the VGCC voltage sensor

to the forces of the EMFs tells us that the current safety guidelines allow us to be

exposed to EMF levels that are something like 7.2 million times too high. That sensitivity

is predicted by the physics. Therefore, the physics and the biology are each pointing to

the same mechanism of action of non-thermal EMFs.

The different effects produced are obviously very deep concerns. They become much

deeper and become existential threats when one considers that several of these effects

are both cumulative and eventually irreversible. There is substantial evidence for the

cumulative nature and eventual irreversibility of the neurological/neuropsychiatric

effects, of the reproductive effects, the mutational DNA effects, the cardiac effects, of

some but not other of the hormonal effects (Chapter 3); any causation of ADHD and

autism may add additional concerns (here the cumulative nature is probably limited

to the perinatal period). When we know that sperm counts have dropped by more

than 50% throughout the technologically advanced countries on earth, it is diffcult

to avoid the conclusion that the vast majority of the population in those countries

is already substantially impacted. The same conclusion can be made based on the

widespread nature of the neuropsychiatric effects in those countries. Both of those

effects will get much much worse even with no increase in current exposures, due to

the cumulative nature and irreversibility of these effects. I expect we will see crash in

human reproduction almost to zero as happened in the Magras and Xenos mouse study

which I estimate to occur within about 5 years, without any increases in our exposures.

Obviously 4G and 5G will make the situation much worse. Similarly I expect that the

deterioration in brain function that we are already seeing will seal our fate if we fail

to act rapidly and vigorously. Our collective brain function may become completely

incapable of dealing with such a mega-crisis situation.

Now it can be argued that some of these may not develop as I expect, although those

expectations are based on the best available evidence. One may even be able to argue

this for all of those expectations. However, when we have substantial risk of multiple

existential threats to every single technologically advanced country on earth, failure

to act vigorously means there is a very high probability of complete destruction of

these societies. And the chaos which would inevitably ensue, in a world that still has

nuclear weapons, may well lead to extinction. In the face of these types or risk, the only

reasonable course is to move with great vigor to stop new exposures and lower current

exposures. One can still access the internet, using wired connections. And we can lower 5GCRISIS the5Gsummit.com 6

cell phone tower and cell phone radiation substantially. Smart meters, if needed, can

work via wired connections.

Over 60% of this document (Chapters 5 & 6), is focused on the failures of statements

from SCENIHR, the telecommunications industry, the U.S. FCC and the U.S. FDA to

refect the science. Their statements repeatedly omit much, often all of the most

important science. Their statements are rife not only with omissions, but also with

easily demonstrable falsehoods and with false logic. These have often occurred at

times where we know that they knew better. These have occurred along with vigorous

efforts by the telecommunications industry to corrupt the science by attacking individual

scientists whose only fault is that they have obtained important fndings that the

industry does not like. These attacks have occurred along with vigorous efforts to

corrupt two agencies that have important regulatory roles.

There are also possible concerns about individual industry-linked research studies.

All wireless communication devices put out polarized EMFs that carry information via

pulsations. Both the pulsations and the polarization make these EMFs much more

biologically active. There are three other factors that also infuence the production of

effects. Several industry-linked studies may have used these factors, along with using

very tiny numbers of individual animals in their studies, to produce studies which may

have been designed to fail (Chapter 5). It is not clear at this point whether this type of

concern is quite limited or whether it is very broad.

The European Commission has done nothing to protect European citizens from any of

these very serious health hazards and the U.S. FDA, EPA and National Cancer Institute

have done nothing to protect American citizens. The U.S. FCC has been much worse

than that, acting vigorously with wanton disregard for our health.5GCRISIS the5Gsummit.com 7

PREFACE

The document that follows was, in its original

form, sent to many of the authorities of the

European Union, in conjunction with other

documents sent to the same people by a group

of European scientists. It was in response two

documents that were, in turn, written by Mr. Ryan

and Dr. Vinciūnas responding to a large group

of European and other international scientists

expressing great concern about the safety of

5G. I was asked by the leaders of the group of scientists to write my own response to

those two documents. Mr. Ryan made the statement that “There is consistent evidence

presented by national and international bodies (International Commission on Non Ionising

Radiation Protection - ICNIRP, Scientifc Committee on Emerging and Newly Identifed

Health Risks (SCENIHR) that exposure to electromagnetic felds does not represent a

health risk, if it remains below the limits set by Council Recommendation 1999/519/EC1.”

In fact, that is not either the ICNIRP or SCENIHR position – their position, and similar

positions have been taken by the U.S. FCC, FDA and the National Cancer Institute, is that

the evidence is inconsistent or conficting and therefore, in their view, no conclusions can

be drawn. Some of these organization have also stated that there is no known mechanism

by which effects can be produced. What is shown below is that there is a vast amount of

evidence in the independent scientifc literature that conficts with both the conclusion

about lack of demonstrated effects and the conclusion about lack of mechanism.

The European Commission, according to the Ryan and Vinciūnas documents and the U.S.

National Cancer Institute, according to their web site, are each depending on the SCENIHR

2015 document to make judgments about EMF effects. Consequently, the reliability

of SCENIHR 2015 is an essential element in determining the reliability of both of their

assessments.

The document that is presented below, differs from the document that was emailed to

EU authorities in three different ways: 1. The original document was sent as an email

with multiple attachments. In this document attachments are simply provided as

citations. The current document is a stand-alone document. 2. Some material is inserted

to discuss positions taken by the U.S. FCC, FDA and National Cancer Institure, so as to

be particularly relevant to the U.S. situation. 3. Substantial additional evidence is also

provided.

The revised document contains seven chapters followed by a citation list for the entire

document.5GCRISIS the5Gsummit.com


wow lota good infor just messily thrown here must reorganize

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