perjantai 12. helmikuuta 2021

Where’s the ruddy virus? Un-freakin’-believable!

  • The COVID vaccines comes from a string of computer-generated codes, not a real virus.
  • There is no fact no real virus: no virus has been isolated, grown in a petri dish, reinfected anyone, or been spread to anyone – Koch’s postulates for defining existence of a virus.
  • Nobody needs this vaccine–why does anyone need to be injected with computer-generated protein codes formulated synthetically in a lab?
  • Please share this information widely, and look for added commentary on this finding from medical journalists and doctors, moving forward.


Where’s the ruddy virus? Un-freakin’-believable!



 

Explosive information from Frances Leader, avid researcher, investigator, and writer, who questioned the UK MHRA and confirmed from them that the RNA genome sequences for the supposed SARS-COV-2 virus being used in the COVID vaccines comes from a string of computer-generated codes, not a real virus.

There is no fact no real virus: no virus has been isolated, grown in a petri dish, reinfected anyone, or been spread to anyone – Koch’s postulates for defining existence of a virus.

What the PCR test is finding is genetic material related to Human Chromosome 8 and found to be common to all living beings; in other words, not a deadly SARS virus but aspects of the living genome shared by all organisms,. . .

The importance of knowing there is no specific organic virus that has been isolated and that is being used in the vaccine cannot be underestimated.

What it implies is that synthetically-manufactured proteins using gene sequencing technology are being injected into human cells, with the intention of altering the human genome and having no connection whatsoever with a putative virus they are supposed to be protecting from.

It also means nobody needs this vaccine–why does anyone need to be injected with computer-generated protein codes formulated synthetically in a lab?

Please share this information widely, and look for added commentary on this finding from medical journalists and doctors, moving forward.

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SOURCE

EMAIL EXCHANGE WITH UK MHRA - Exposing the genomic sequence of SARSCov2

francesleader (58)in #worldnews • 2 months ago (edited)




Explosive information from Frances Leader, avid researcher, investigator, and writer, who questioned the UK MHRA and confirmed from them that the RNA genome sequences for the supposed SARS-COV-2 virus being used in the COVID vaccines comes from a string of computer-generated codes, not a real virus. There is no fact no real virus: no virus has been isolated, grown in a petri dish, reinfected anyone, or been spread to anyone--Koch's postulates for defining existence of a virus. What the PCR test is finding is genetic material related to Human Chromosome 8 and found to be common to all living beings; in other words, not a deadly SARS virus but aspects of the living genome shared by all organisms, possibly, Or exosomes from the actions of cells reacting to stresses caused possibly by electromagnetic radiation, specifically 5G--which is still being rolled out worldwide. The importance of knowing there is no specific organic virus that has been isolated and that is being used in the vaccine cannot be underestimated. What it implies is that synthetically-manufactured proteins using gene sequencing technology are being injected into human cells, with the intention of altering the human genome and having no connection whatsoever with a putative virus they are supposed to be protecting from. It also means nobody needs this vaccine--why does anyone need to be injected with computer-generated protein codes formulated synthetically in a lab? Please share this information widely, and look for added commentary on this finding from medical journalists and doctors, moving forward.


When I read the Wuhan study in Feb 2020 I was mortified by the monkey kidney & foetal cell-lines which were used as a "culture" before rt-PCR amplification. Isolation was never satisfactory at any stage thereafter.

I honestly felt sick.
The genome sequence was computed from this.

I set about proving that the vaccine has been created from a computer generated genomic sequence & not one isolated from an infected person, either in Wuhan or anywhere else in the world since.

The Pfizer BioNTech vaccine was approved by UK MHRA (Medicines and Healthcare products Regulatory Agency) & I initiated a polite exchange of emails with them as follows:

MHRA Email 1.png

MHRA Email 2.png

MHRA Email 3.png

MHRA Email 4.png

MHRA 5.png

MHRA 6.png

MHRA 7.png

MHRA 8.png

Twitter post yesterday & my account was summarily suspended:

MHRA 9 - twitter suspension notice.png

WITHOUT A PURIFIED SAMPLE VIRUS UK MHRA CONFESSES THAT THE PFIZER VACCINE mRNA ELEMENT IS A COMPUTER GENERATED GENOMIC SEQUENCE AMPLIFIED FROM A RNA FRAGMENT FOUND IN ONE EXPERIMENTAL STUDY FROM WUHAN (Feb 2020).
NO SIMILAR VIRUS HAS BEEN ISOLATED ANYWHERE IN THE WORLD SINCE.
THE VACCINES ARE CREATED USING A COMPUTER MODEL!
AFTER NEIL FERGUSON'S CATASTROPHIC COMPUTER MODEL TOOK THE WORLD INTO A SPIRAL OF LOCKDOWNS, MASKS & ABJECT FEAR - HOW MUCH FAITH HAVE YOU GOT IN A COMPUTER CREATED "VIRAL" SPIKE PROTEIN BEING INJECTED INTO YOUR BLOODSTREAM?

Several followers asked for sight of the original exchange of emails & as twitter suspended me over this revelation I decided to create this article which, being on the blockchain, is safe from deletion.

Thanks to all followers on all social media channels for disseminating my work.

Much love as ever

Fran
xx

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Koch's postulates

From Wikipedia, the free encyclopedia
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Robert Hermann Koch (11 December 1843 – 27 May 1910) was a German physician who developed Koch's postulates.[1]

Koch's postulates (/ˈkɔːx/)[2] are four criteria designed to establish a causative relationship between a microbe and a disease. The postulates were formulated by Robert Koch and Friedrich Loeffler in 1884, based on earlier concepts described by Jakob Henle,[3] and refined and published by Koch in 1890. Koch applied the postulates to describe the etiology of cholera and tuberculosis, but they have been controversially generalized to other diseases. These postulates were generated before modern concepts in microbial pathogenesis that cannot be examined using Koch's postulates, including viruses (which are obligate cellular parasites) and asymptomatic carriers. They have largely been supplanted by other criteria such as the Bradford Hill criteria for infectious disease causality in modern public health.

The postulates[edit]

Koch's postulates of disease.

Koch's postulates are the following:

  1. The microorganism must be found in abundance in all organisms suffering from the disease, but should not be found in healthy organisms.
  2. The microorganism must be isolated from a diseased organism and grown in pure culture.
  3. The cultured microorganism should cause disease when introduced into a healthy organism.
  4. The microorganism must be reisolated from the inoculated, diseased experimental host and identified as being identical to the original specific causative agent.

However, Koch later abandoned the universalist requirement of the first postulate altogether when he discovered asymptomatic carriers of cholera[4] and, later, of typhoid feverAsymptomatic or subclinical infection carriers are now known to be a common feature of many infectious diseases, especially viral diseases such as polioherpes simplexHIV/AIDS, and hepatitis C. As a specific example, all doctors and virologists agree that poliovirus causes paralysis in just a few infected subjects.

The second postulate may also be suspended for certain microorganisms or entities that cannot (at the present time) be grown in pure culture.[5] Viruses also require host cells to grow and reproduce and therefore cannot be grown in pure cultures.

The third postulate specifies "should" not "must" because, as Koch himself proved in regard to both tuberculosis and cholera,[6] not all organisms exposed to an infectious agent will acquire the infection. Noninfection may be due to such factors as general health and proper immune functioning; acquired immunity from previous exposure or vaccination; or genetic immunity, as with the resistance to malaria conferred by possessing at least one sickle cell allele.

There are a few other exceptions to Koch's postulates. A single pathogen can cause several disease conditions. Additionally, a single disease condition can be caused by several different microorganisms. Some pathogens cannot be cultured in the lab, and some pathogens only cause disease in humans.[7]

In summary, an infectious agent can be considered to be a sufficient cause for a disease if it satisfies Koch's postulates. Failing that, it suggests that the infectious agent is a necessary, but insufficient, cause for a disease.

History[edit]

Koch's postulates were developed in the 19th century as general guidelines to identify pathogens that could be isolated with the techniques of the day.[8] Even in Koch's time, it was recognized that some infectious agents were clearly responsible for disease even though they did not fulfill all of the postulates.[4][6] Attempts to apply Koch's postulates rigidly to the diagnosis of viral diseases in the late 19th century, at a time when viruses could not be seen or isolated in culture, may have impeded the early development of the field of virology.[9][10] Koch's postulates have been recognized as largely obsolete by epidemiologists since the 1950s,[11][12] so, while retaining historical importance and continuing to inform the approach to microbiologic diagnosis, they are not routinely used to demonstrate causality.

Koch's postulates have also influenced scientists who examine microbial pathogenesis from a molecular point of view. In the 1980s, a molecular version of Koch's postulates was developed to guide the identification of microbial genes encoding virulence factors.[13]

That HIV causes AIDS does not follow from Koch's postulates,[14] which may have supported HIV/AIDS denialism. The role of oncoviruses in causing some cancers also does not follow Koch's postulates.[15]

New discoveries of methods of infections as a result of Koch and many others' work have shown that some diseases and conditions are not always caused by a single microbe species. According to a study by Oliver A. Todd and Brain M Peters, a newly discovered interaction between the pathogen Staphylococcus aureus and "fungal opportunist" Candida albicans is being considered a co-infection that is found in the bodies of sick patients who suffer from different conditions [2019]. This kind of synergism was found to be lethal in a separate study conducted by Carlson on mice. When mice were infected with the two pathogens independently, sickness resulted but the mice were able to recover. When infected with both pathogens together, the mice had a near-100% mortality rate, showing that some pathogens cannot be as easily isolated or may need extra techniques and steps that better prove causation of the disease.[16]

For the 21st century[edit]

Koch's postulates have played an important role in microbiology, yet they have major limitations. For example, Koch was well aware in the case of cholera that the causal agent, Vibrio cholerae, could be found in both sick and healthy people, invalidating his first postulate. Furthermore, viral diseases were not yet discovered when Koch formulated his postulates, and there are many viruses that do not cause illness in all infected individuals, a requirement of the first postulate. Additionally, it was known through experimentation that Helicobacter pylori caused mild inflammation of the gastric lining when ingested. As evident as the inflammation was, it still did not immediately convince skeptics that H. pylori was associated with ulcers. Eventually, skeptics were silenced when a newly developed antibiotic treatment eliminated the bacteria and ultimately cured the disease. Koch's postulates are also of limited effectiveness when evaluating biofilms, Somni cells, and viruses. Cultivation of biofilms requires cultivation by molecular methods rather than traditional methods, and these alternative methods do not detect the cause of infection, which therefore interferes with the third postulate, that microorganisms should cause disease.[17] Somni cells and viruses cannot be cultured. The Somni cells, also called sleeping cells, become dormant due to strain on the cell. This state of sleep prevents the cell from growing in the culture.[18] This is similar to how viruses cannot grow in axenic culture: viruses must be living to replicate, so the culture is not a suitable host.[19] Allyson Byrd and Julia Segre have proposed changes to the postulates to make them more accurate for today's world. Their revisions involve the third postulate: they disagree that a pathogen will always cause disease. Their first revision involves colonization resistance. Colonization resistance allows an organism to feed off of the host and protect it from pathogens that would have caused disease if the organism was not attached to the host. Their second revision is that a community of microbes could help inhibit pathogens even further, preventing the pathogen from spreading disease as it is supposed to.[20] Similar to Byrd and Segre, Thomas Rivers suggested revisions to Koch's postulates. He believed that, although the original postulates were made as a guide, they were actually an obstacle. Rivers wanted to show the link between viruses and diseases. Rivers cultivated his own postulates; the first stated that the virus must be connected to disease consistently. Secondly, the outcome of experimentation must indicate that the virus is directly responsible for the disease.[21] Contradictions and occurrences such as these have led many to believe that a fifth postulate may be required. If enacted, this postulate would state that sufficient microbial data should allow scientists to treat, cure, or prevent the particular disease.

More recently, modern nucleic-acid-based microbial detection methods have made Koch's original postulates even less relevant. These methods enable the identification of microbes that are associated with a disease, but which cannot be cultured. Also, these methods are very sensitive, and can often detect very low levels of viruses in healthy people.

These new methods have led to revised versions of Koch's postulates. Fredricks and Relman have suggested the following postulates for the 21st century:[22]

  1. A nucleic acid sequence belonging to a putative pathogen should be present in most cases of an infectious disease. Microbial nucleic acids should be found preferentially in those organs or gross anatomic sites known to be diseased, and not in those organs that lack pathology.
  2. Fewer, or no, copies of pathogen-associated nucleic acid sequences should occur in hosts or tissues without disease.
  3. With resolution of disease, the copy number of pathogen-associated nucleic acid sequences should decrease or become undetectable. With clinical relapse, the opposite should occur.
  4. When sequence detection predates disease, or sequence copy number correlates with severity of disease or pathology, the sequence-disease association is more likely to be a causal relationship.
  5. The nature of the microorganism inferred from the available sequence should be consistent with the known biological characteristics of that group of organisms.
  6. Tissue-sequence correlates should be sought at the cellular level: efforts should be made to demonstrate specific in situ hybridization of microbial sequence to areas of tissue pathology and to visible microorganisms or to areas where microorganisms are presumed to be located.
  7. These sequence-based forms of evidence for microbial causation should be reproducible.

These modifications are still controversial in that they do not account well for established disease associations, such as papillomavirus and cervical cancer, nor do they take into account prion diseases, which have no nucleic acid sequences of their own.

https://en.wikipedia.org/wiki/Koch's_postulates

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