lauantai 20. helmikuuta 2021

Your Coronavirus Test Is Positive. Maybe It Shouldn’t Be.

  • The PCR test amplifies genetic matter from the virus in cycles; the fewer cycles required, the greater the amount of virus, or viral load, in the sample.
  • The greater the viral load, the more likely the patient is to be contagious.
  • The C.D.C.’s own calculations suggest that it is extremely difficult to detect any live virus in a sample above a threshold of 33 cycles.
  • WHO Admits High-Cycle PCR Tests Produce COVID False Positives.
  • Proof that COVID-19 Statistics are Being Padded With Influenza Cases.
  • Researchers Uncover How the CDC Illegally Inflated COVID-19 Death Statistics


Your Coronavirus Test Is Positive. Maybe It Shouldn’t Be.

The usual diagnostic tests may simply be too sensitive and too slow to contain the spread of the virus


By Apoorva Mandavilli | The New York Times | 

THE NEW YORK TIMES -- Some of the nation’s leading public health experts are raising a new concern in the endless debate over coronavirus testing in the United States: The standard tests are diagnosing huge numbers of people who may be carrying relatively insignificant amounts of the virus.

Most of these people are not likely to be contagious, and identifying them may contribute to bottlenecks that prevent those who are contagious from being found in time. But researchers say the solution is not to test less, or to skip testing people without symptoms, as recently suggested by the Centers for Disease Control and Prevention.

Instead, new data underscore the need for more widespread use of rapid tests, even if they are less sensitive.

“The decision not to test asymptomatic people is just really backward,” said Dr. Michael Mina, an epidemiologist at the Harvard T.H. Chan School of Public Health, referring to the C.D.C. recommendation.

“In fact, we should be ramping up testing of all different people,” he said, “but we have to do it through whole different mechanisms.”

In what may be a step in this direction, the Trump administration announced on Thursday that it would purchase 150 million rapid tests.

The most widely used diagnostic test for the new coronavirus, called a PCR test, provides a simple yes-no answer to the question of whether a patient is infected.

But similar PCR tests for other viruses do offer some sense of how contagious an infected patient may be: The results may include a rough estimate of the amount of virus in the patient’s body.

“We’ve been using one type of data for everything, and that is just plus or minus — that’s all,” Dr. Mina said. “We’re using that for clinical diagnostics, for public health, for policy decision-making.”

But yes-no isn’t good enough, he added. It’s the amount of virus that should dictate the infected patient’s next steps. “It’s really irresponsible, I think, to forgo the recognition that this is a quantitative issue,” Dr. Mina said.

The PCR test amplifies genetic matter from the virus in cycles; the fewer cycles required, the greater the amount of virus, or viral load, in the sample. The greater the viral load, the more likely the patient is to be contagious.

This number of amplification cycles needed to find the virus, called the cycle threshold, is never included in the results sent to doctors and coronavirus patients, although it could tell them how infectious the patients are.

In three sets of testing data that include cycle thresholds, compiled by officials in Massachusetts, New York and Nevada, up to 90 percent of people testing positive carried barely any virus, a review by The Times found.

On Thursday, the United States recorded 45,604 new coronavirus cases, according to a database maintained by The Times. If the rates of contagiousness in Massachusetts and New York were to apply nationwide, then perhaps only 4,500 of those people may actually need to isolate and submit to contact tracing.

One solution would be to adjust the cycle threshold used now to decide that a patient is infected. Most tests set the limit at 40, a few at 37. This means that you are positive for the coronavirus if the test process required up to 40 cycles, or 37, to detect the virus.

Tests with thresholds so high may detect not just live virus but also genetic fragments, leftovers from infection that pose no particular risk — akin to finding a hair in a room long after a person has left, Dr. Mina said.

Any test with a cycle threshold above 35 is too sensitive, agreed Juliet Morrison, a virologist at the University of California, Riverside. “I’m shocked that people would think that 40 could represent a positive,” she said.

A more reasonable cutoff would be 30 to 35, she added. Dr. Mina said he would set the figure at 30, or even less. Those changes would mean the amount of genetic material in a patient’s sample would have to be 100-fold to 1,000-fold that of the current standard for the test to return a positive result — at least, one worth acting on.

The Food and Drug Administration said in an emailed statement that it does not specify the cycle threshold ranges used to determine who is positive, and that “commercial manufacturers and laboratories set their own.”

The Centers for Disease Control and Prevention said it is examining the use of cycle threshold measures “for policy decisions.” The agency said it would need to collaborate with the F.D.A. and with device manufacturers to ensure the measures “can be used properly and with assurance that we know what they mean.”

The C.D.C.’s own calculations suggest that it is extremely difficult to detect any live virus in a sample above a threshold of 33 cycles. Officials at some state labs said the C.D.C. had not asked them to note threshold values or to share them with contact-tracing organizations.

For example, North Carolina’s state lab uses the Thermo Fisher coronavirus test, which automatically classifies results based on a cutoff of 37 cycles. A spokeswoman for the lab said testers did not have access to the precise numbers.

This amounts to an enormous missed opportunity to learn more about the disease, some experts said.

“It’s just kind of mind-blowing to me that people are not recording the C.T. values from all these tests — that they’re just returning a positive or a negative,” said Angela Rasmussen, a virologist at Columbia University in New York.

“It would be useful information to know if somebody’s positive, whether they have a high viral load or a low viral load,” she added.

Officials at the Wadsworth Center, New York’s state lab, have access to C.T. values from tests they have processed, and analyzed their numbers at The Times’s request. In July, the lab identified 794 positive tests, based on a threshold of 40 cycles.

With a cutoff of 35, about half of those tests would no longer qualify as positive. About 70 percent would no longer be judged positive if the cycles were limited to 30.

In Massachusetts, from 85 to 90 percent of people who tested positive in July with a cycle threshold of 40 would have been deemed negative if the threshold were 30 cycles, Dr. Mina said. “I would say that none of those people should be contact-traced, not one,” he said.

Other experts informed of these numbers were stunned.

“I’m really shocked that it could be that high — the proportion of people with high C.T. value results,” said Dr. Ashish Jha, director of the Harvard Global Health Institute. “Boy, does it really change the way we need to be thinking about testing.”

Dr. Jha said he had thought of the PCR test as a problem because it cannot scale to the volume, frequency or speed of tests needed. “But what I am realizing is that a really substantial part of the problem is that we’re not even testing the people who we need to be testing,” he said.

The number of people with positive results who aren’t infectious is particularly concerning, said Scott Becker, executive director of the Association of Public Health Laboratories. “That worries me a lot, just because it’s so high,” he said, adding that the organization intended to meet with Dr. Mina to discuss the issue.

The F.D.A. noted that people may have a low viral load when they are newly infected. A test with less sensitivity would miss these infections.

But that problem is easily solved, Dr. Mina said: “Test them again, six hours later or 15 hours later or whatever,” he said. A rapid test would find these patients quickly, even if it were less sensitive, because their viral loads would quickly rise.

PCR tests still have a role, he and other experts said. For example, their sensitivity is an asset when identifying newly infected people to enroll in clinical trials of drugs.

But with 20 percent or more of people testing positive for the virus in some parts of the country, Dr. Mina and other researchers are questioning the use of PCR tests as a frontline diagnostic tool.

People infected with the virus are most infectious from a day or two before symptoms appear till about five days after. But at the current testing rates, “you’re not going to be doing it frequently enough to have any chance of really capturing somebody in that window,” Dr. Mina added.

Highly sensitive PCR tests seemed like the best option for tracking the coronavirus at the start of the pandemic. But for the outbreaks raging now, he said, what’s needed are coronavirus tests that are fast, cheap and abundant enough to frequently test everyone who needs it — even if the tests are less sensitive.

“It might not catch every last one of the transmitting people, but it sure will catch the most transmissible people, including the superspreaders,” Dr. Mina said. “That alone would drive epidemics practically to zero.”

https://cnas.ucr.edu/media/2020/08/29/your-coronavirus-test-positive-maybe-it-shouldnt-be

Read the original article here:

VIEW ARTICLE


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WHO Admits High-Cycle PCR Tests Produce COVID False Positives

Written by Tyler Durden

Were the ‘conspiracy theorists’ just proven right about the “fake rescue plan” for COVID? Did the ‘science-deniers’ just get confirmation that it was political after all?

The short answer to both of these questions regarding the COVID-19 ‘casedemic’ and the fallacy of asymptomatic PCR testing is YES and YES!

We have detailed the controversy surrounding America’s COVID “casedemic” and the misleading results of the PCR test and its amplification procedure in great detail over the past few months.

As a reminder, “cycle thresholds” (Ct) are the level at which widely used polymerase chain reaction (PCR) test can detect a sample of the COVID-19 virus. The higher the number of cycles, the lower the amount of viral load in the sample; the lower the cycles, the more prevalent the virus was in the original sample.

Numerous epidemiological experts have argued that cycle thresholds are an important metric by which patients, the public, and policymakers can make more informed decisions about how infectious and/or sick an individual with a positive COVID-19 test might be. However, as JustTheNews reports, health departments across the country are failing to collect that data.

In fact, as far back as October, we brought the world’s attention to the COVID-19 “casedemic” and the disturbing reality of high-cycle threshold PCR tests being worse than useless as indicators of COVID-19 “sickness”. PJMedia’s Stacey Lennox said at the time:

Biden will issue national standards, like the plexiglass barriers in restaurants he spoke about during the debate, and pressure governors to implement mask mandates using the federal government’s financial leverage.

Some hack at the CDC or FDA will issue new guidance lowering the Ct the labs use, and cases will magically start to fall.

In reality, the change will only eliminate false positives, but most Americans won’t know that.

Good old Uncle Joe will be the hero, even though it is Deep-State actors in the health bureaucracies who won’t solve a problem with testing they have been aware of for months. TDS is a heck of a drug.

And now, as Lennox explains in detail below, we have been proved 100% correct as less than one hour after President Biden’s inauguration, the WHO proved us right.

In August of last year, The New York Times published an article stating that as many as 90% of COVID-19 tests in three states were not indicative of active illness. In other words, they were picking up viral debris incapable of causing infection or being transmitted because the cycle threshold (Ct) of the PCR testing amplified the sample too many times.

Labs in the United States were using a Ct of 37-40. Epidemiologists interviewed at the time said a Ct of around 30 was probably more appropriate. This means the CDC’s COVID-19 test standards for the PCR test would pick up an excessive number of false positives. The Times report noted the CDC’s own data suggested the PCR did not detect live virus over a Ct of 33. The reporter also noted that clinicians were not receiving the Ct value as part of the test results.

Yet a PCR test instruction document from the CDC that had been revised five times as of July 13, 2020, specified testing and interpretation of the test using a Ct of 40. On September 28, 2020, a study published in the journal Clinical Infectious Diseases from Jaafar et al. had asserted, based on patient labs and clinical data involving nearly 4,000 patients, that a Ct of 30 was appropriate for making public policy. An update to the CDC instructions for PCR testing from December 1, 2020, still uses a Ct of 40.

Shortly before the New York Times article was published, the CDC revised its COVID-19 test recommendations, saying that only syptomatic patients should be tested. The media went insane, and Dr. Fauci went all over television saying he was not part of the decision to change the testing standards:

“I am concerned about the interpretation of these recommendations and worried it will give people the incorrect assumption that asymptomatic spread is not of great concern. In fact it is.”

So, of course, the Mendacious Midget™ had spoken, and the guidelines went back to testing everyone, all the time, with an oversensitive test.

The idea that asymptomatic spread was a concern as of August was just one of many lies Dr. Fauci told. At the beginning of the pandemic in late January, he said:

The one thing historically that people need to realize is that even if there is some asymptomatic transmission, in all the history of respiratory borne viruses of any type, asymptomatic transmission has never been the driver of outbreaks. The driver of outbreaks is always a symptomatic person. Even if there is a rare asymptomatic person that might transmit, an epidemic is not driven by asymptomatic carriers.

There is not a single study or meta-analysis that differs from Fauci’s original assessment.

Today, within an hour of Joe Biden being inaugurated and signing an executive order mandating masks on all federal property, the WHO sent out a notice to lab professionals using the PCR test. It said:

WHO guidance Diagnostic testing for SARS-CoV-2 states that careful interpretation of weak positive results is needed (1).

The cycle threshold (Ct) needed to detect virus is inversely proportional to the patient’s viral load.

Where test results do not correspond with the clinical presentation, a new specimen should be taken and retested using the same or different NAT technology.

This translates to “in the absence of symptoms, a high Ct value means you are highly unlikely to become ill or get anyone else sick in the absence of very recent exposure to an infected person.”

Dr. Fauci knew this in July when he said that tests with a Ct above 35 were likely picking up viral debris or dead virus.

Even at a Ct of 35, the incidence of virus samples that could replicate is very low, according to Jaafar et al.

The only state I know that requires reporting the Ct with every test is Florida, which started this policy in December.

The WHO went on, stating:

Most PCR assays are indicated as an aid for diagnosis, therefore, health care providers must consider any result in combination with timing of sampling, specimen type, assay specifics, clinical observations, patient history, confirmed status of any contacts, and epidemiological information.

In short, a positive PCR test in the absence of symptoms means nothing at a Ct of higher than 30, according to the experts interviewed by the New York Times and according to Jaafar et al. Yet positive tests is the number CNN loves flashing on the screen.

If the percentage found by the Times in August holds, there have been approximately 2.43 million actual cases to date, not 24.3 million.

There is also no way to calculate the deaths from COVID-19 rather than deaths with some dead viral debris in the nostrils.

What I have referred to as the “casedemic” since September will be magically solved just in time for Joe Biden to look like a hero. For doing absolutely nothing.

Do not tell me there is not a politicized deep state in our health agencies. Do not ever tell me I need to listen to Dr. Anthony Fauci again. And every business owner who has been ruined because of lockdowns due to a high number of “cases” should be livid. Any parent whose child has lost a year of school should be furious.

None of this was for your health. It was to get rid of Orange Man Bad.

As an aside, this also clearly explains the disappearance of the “flu” during this season as the plethora of high Ct PCR Tests supposedly pointing to a surge in COVID are nothing of the sort.

As Stephen Lendman noted previously, claiming “lockdowns stopped flu in its tracks, (outbreaks) plummet(ting) by 98% in the United States” ignored that what’s called COVID is merely seasonal influenza combined with false positives (extremely high Ct) from PCR-Tests.

And for that reason, the great 2020 disappearing flu passes largely under the mass media’s radar. Media proliferated mass deception and the power of repetition get most people to believe and having successfully “killed the flu”, they will now do the same with COVID… and, if allowed by our betters, we will all return to the new normal they desire.

https://principia-scientific.com/doctors-nurses-giving-covid-19-vaccine-will-be-tried-as-war-criminals/?utm_source=feedburner&utm_medium=email&utm_campaign=Feed%3A+psintl+%28Principia+Scientific+Intl+-+Latest+News%29

Read more at www.zerohedge.com


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Proof that COVID-19 Statistics are Being Padded With Influenza Cases


Below are a series of three short videos of an interview by software engineer and statistician John Cullen of Dr. (and State Senator) Scott Jensen. While Cullen calls Dr. Jensen a hero, and he is, Cullen is every bit worthy of that accolade. I cannot do justice with the treasure of information coming from these two patriots, and so I will set forth below my simple explanation of the World Health Organization (WHO) influenza data discussed by Cullen. The charts reveal that the COVID-19 statistics are being padded by falsely reporting influenza cases as COVID-19 cases.

To suggest that influenza cases are being misrepresented as COVID-19 cases is simply not allowed to be mentioned in the mainstream media. Peter Andrews, writing for Russia Today, reveals that there has been a 98% plummet in flu infections. He then reveals it is impolite within the scientific community to suggest that doctors are misclassifying influenza cases as COVID-19 cases. Andrews explains that “it only seems like the flu has disappeared because doctors and scientists have been wrongly classing other respiratory diseases as Covid. Please note that the boffins are already treating this suggestion as something akin to flat-Earth theory.”

Andrews reveals that “Australia essentially ‘skipped’ their flu season this year, with not a single case reported since July (their peak). In fact, flu has more or less vanished throughout the Southern Hemisphere.”  Andrews was writing on October 29, 2020. The Southern Hemisphere had emerged from what should have been their fall and winter flu season. But they had none. And the Northern Hemisphere since followed suit with a collapse in reported flu cases. Jo MacFarlane reporting for The Daily Mail concluded from the WHO data that “flu, it seems, has all but vanished.”

MacFarlane published his article on October 24, 2020, which was the beginning of what is supposed to be the fall and winter flu season in the Northern Hemisphere. MacFarlane could already see from the data that the expected seasonal flu epidemic was not making its appearance. The reported flu cases in the UK were down approximately 90%. He saw the disappearance of the flu revealed by “the figures provide a startling insight into what has become a creeping trend across the world.”

Of course, MacFarlane states the obvious. “There are those who claim flu cases haven’t vanished at all, but are instead being recorded as Covid-19.” But after making that common-sense statement, MacFarlane quickly dismisses the thought. So, what is the explanation he announces for the disappearance of the flu in the midst of the alleged COVID-19 pandemic? It is the theory of … wait for it … “viral interference.”

MacFarlane explains that “[w]hen an individual is infected with one virus, they are less likely to be infected by another during that time due to something called ‘viral interference’.” MacFarlane quotes Dr. Elisabetta Groppelli who claims that “[v]iruses are parasites. Once they enter a cell, they don’t want other viruses to compete with. So the virus already in the body will effectively kick the other parasite out.” It sounds good, but it is not true. Indeed, when one’s immune system is focused on fighting off one particular pathogen, the body’s immune resources are focused on that pathogen. With all of the body’s immune resources focused on that one pathogen, the person does not have the reserves to fight an unrelated pathogen and is thus is more susceptible to an unrelated pathogen.

That is why the flu vaccine only works for the particular strain of the flu virus that is in the vaccine and no others. Often, persons who receive the flu vaccine end up getting the flu, but it is a different strain of the flu for which they have no protection. Under the theory of ‘viral interference’ the patient getting a flu shot should be protected from all strains of flu and not just the strain in the vaccine.

The phenomenon of a vaccinated person being more susceptible to an unrelate pathogen is known as pathogenic priming. Vaccines cause pathogenic priming, which injures a person’s immune system such that the person is 4.4 times more likely to become ill from some other pathogen. For example, at least six major studies have shown that a person who gets the flu shot has had their immune system pathogenically primed to be more likely to become infected from coronavirus.

The charts below reveal a complete collapse in worldwide cases of influenza after COVID-19 made its appearance in the spring of 2020. Notice the complete disappearance of the flu during the 2020-2021 fall and winter seasonal flu period. That disappearance of flu correlates directly with the reported second-wave of COVID-19 cases and suggests that flu cases are being misreported as COVID-19 second-wave cases.



https://greatmountainpublishing.com/2021/02/03/proof-that-covid-19-statistics-are-being-padded-with-influenza-cases/

HEROES: Tribute to Dr Scott Jensen – Part 1
HEROES: Tribute to Dr Scott Jensen w/ John Cullen – Part 2
The Final Chapter: Part 3 – HEROES: A Tribute to Dr Scott Jensen


Researchers Uncover How the CDC Illegally Inflated COVID-19 Death Statistics

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lauantai 13. helmikuuta 2021

Sara Stickles: 28-year-old has brain aneurysm, dead five days after second Pfizer mRNA shot

 

Sara Stickles: 28-year-old has brain aneurysm, dead five days after second Pfizer mRNA shot

TheCOVIDBlog



Ms. Sara Stickles


BELOIT, WISCONSIN — Sara Stickles shared a Facebook post on February 6 talking about reverse karma.



The young healthcare worker’s life was essentially extinguished the very next day.

Ms. Stickles received the second dose of the Pfizer mRNA shot on or around February 2, according to a family Facebook post. She immediately broke out in rashes. Ms. Stickles had severe headaches five days later, Sunday, February 7. Soon thereafter, she started crying and said “something isn’t right.” She lost the ability to speak, her eyes crossed and glazed over, before she lost consciousness, according to a Facebook post by Jacqueline F. Gifford.

She was taken to SwedishAmerican Hospital, just over the state line from Beloit. The initial diagnosis was a ruptured brain aneurysm. She was then airlifted to the University of Wisconsin Hospital in Madison the next day, according to her uncle, George Allen Petit.

Doctors performed a cerebral angiography through her groin all the way up to her brain. Subarachnoid hemorrhage was also mentioned as the possible issue.

Kara Stickles, Sara’s twin sister, posted an update on February 10. Sara “has no brain activity,” she said.
Doctors called the family and summonsed them to the hospital to say their goodbyes.
She died yesterday.





Sara Stickles in the hospital.




Sara’s legacy


Ms. Stickles, 28, leaves behind a young son. It appears she had just began a job at SwedishAmerican Hospital within the last several months. Ms. Stickles is an organ donor. So doctors are keeping her body alive until it is time to harvest said organs. She was a big fan of Eminen and the movie “Love and Basketball.” The family set up a GoFundMe page to help pay for the funeral expenses.

COVID Legal USA today is extremely busy helping American fight back against mandatory vaccines for employment and other COVID mandates. Contact us today and a legal writer will get back to you within 24 hours.


Fight back against censorship. PLEASE SUPPORT US VIA PAYPAL.

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Ruptured Aneurysm


https://www.youtube.com/watch?v=-99Lyl3h6QY

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https://www.slideshare.net/avinash0025/unruptured-brain-aneurysm

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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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