The Controversial Purnima Wagh's No "SARS-CoV-2 virus" story.

Many roads lead to there being NO Invisible "isolated SARS-CoV-2 virus" circulating in 2020+. Sadly the "Health Freedom Movement" behaved like Pharmakeia's controlled opposition around this story.

This story was resisted by the “Health Freedom Movement” and Globalist Fact-Checkers alike. Purnima Wagh’s credentials were scrutinized and her findings were dismissed without giving her a fair chance to explain her qualifications. I Prunima Wagh exposed an extremely important truth. I have long suspected “Gain-of-Function Bird Flu” promoter Robert Redfield as being a Controlled Opposition operative needed for PLANdemic Stage 2 mind games and Prunima’s communications with Redfield affirms, to me, he is just playing his part in the Globalist’s plot.

Purnima EXPOSES that China was measuring the “isolate” against an EXISTING SEQUENCE. This is massively important concerning HOW they were capable of producing the DESIRED SEQUENCE they planned for. My article - Genetic Sequencing and its Deceptive Pitfalls (here) deals with this issue of MATCHING an “isolate” to a PRE-SELECTED SEQUENCE. Dr. Stefan Lanka has shown how one can find any PRE-SELECTED SEQUENCE in anyone. I have long suspected this is how this crime was done i.e. the “original isolate” was aligned with the Computer Sequence sent from Dr. Ralph Barik of University Chapell Hill USA (possibly modified with an HIV insert in the Wuhan Lab).

Watch the following video -
Purnima’s introduction to staging the PLANdemic and her views on how 5G was involved with creating novel flu-like symptoms concur with my research (here).
Purnima Wagh said she had $1.5M to do the isolation work and they found nothing.

• COVID SCAMDEMIC IS BASED ON VIRUS THAT NEVER WAS (here)

Dr. Lee Merritt interviews Purnima Wagh regarding the misdirecting accusations regarding her credentials by the Virus Believers.

• DR MERRITT AND POORNIMA WAGH PHD VIROLOGY (here)
  

Notes for Purnima Wagh’s Findings

My lab Isolation, Purification, Characterization, and Causation findings:

• In mid-April 2020, I was contracted by the Principal Investigator (chief scientist of the lab I previously had worked in. I’m keeping all lab names and locations private due to security issues), saying they had received 1,500 Covid positive samples from all over Southern California and they needed to be stringently tested via isolation, purification, etc. We had received a HUGE $1.5 million grant from NIH which was to be used for the isolation of the NOVEL.

• I agreed to do the studies, provided I was given FREE rein to do the isolation, purification, characterization, and causation studies according to my previous training in pathology and microbiology as a clinical lab scientist, not by virology standards of testing. After much back and forth, the principal investigator (PI) RELUCTANTLY agreed.

• 20 lab members headed by me as the senior lab scientist commenced the isolation, purification, characterization, and causation studies on these 1500 samples in late April 2020 in the same EXACTING and Scientifically accurate manner as I’ve described in previous slides. These studies finally ended in September 2020 as we did the studies in 3 separate batches as our lab PI (principal investigator) insisted we did. After the first attempt, all we found was decomposing Human cellular debris (that is what a virus really is) We found identical results in the next two attempts. The PI made us do 3 rounds of testing using the lame excuse of cross-contamination and poor scientific protocols in the lab.

• As far as the caution studies with the 4 Koch’s Postulates go, we used ferrets as our subjects and had ferrets for the control groups as well. The control group of another 100 ferrets were injected with saline solution.
  . After 3 rounds of extensive testing, we found only Human cellular debris, there was no sign of an INTACT 30.000 to 40,000 base pair or anything even remotely close to the “In Silico” genome of the SARS COV 2 virus after all the biochemical analysis was performed.

• In fact, the ferrets that were injected with the isolated, purified SARS COV 2 positive samples, were in excellent shape. They never experienced fevers, runny noses, bilateral pneumonia, or hypoxia (lack of oxygen) like symptoms that the human counterparts who were COVID-19 positive were experiencing. The only small side effect we noticed was that 10 were extremely active, had great appetites, and some even put on weight. These are NOT characteristics of any sickness I would recognize. And remember! The test subjects have to show the same exact symptoms of the disease as the infected humans the samples came from.

• These results were then discussed with SELECT other university labs across the country, after which, 6 other university labs decided to replicate our studies with the same exact methodology as we had followed in our lab. The Result they found what we found – human cellular debris, no trace of any virus remotely close to SARS-COV 2

• Of the 7 labs (including our lab) 6 of which are in California and one on the east coast decided to contact the CDC regarding our findings. The chilling reception we got from Rober Redfield ( The hook-nosed Gnome, Fauci’s colleague and Trump appointee as CDC director) was not surprising for me but was mind-boggling for most of the other scientists.

• Redfield over a 2.5-hour Zoom call came straight to the point. He said call it SARS CoV 2, I don’t care what you found. If you don’t call it SARS-CoV2, you will never have a job again, never work in a lab again, your labs might lose all funding, and might just get closed down. We all declined to go along. Our lab decided to publish our findings and as of today, 21 journals have officially chickened out and refused to publish us. This includes prestigious journals like Nature, Science, Plos One, DMJ (Danish Medical Journal), etc.

• Over a two month period from June 2020 to early August 2020, we urged the CDC to send us just one isolated, purified sample of SARS CoV2. First, they said they could not, then they said they had no sample to send and then after the 2-month mark of constant badgering, they would just hang up on us. All e-mail requests regarding overnighting us a sample of SARS-CoV2 went on deaf ears and were completely ignored. We became pariahs.

• Our Lab was raided by the FBI in late April 2021. All Computers, drafts, paperwork, etc. were confiscated and probably destroyed. Fortunately, we had saved a backed up all drafts and paperwork. Two members of my lab apparently committed suicide in August 2021 and one in early February 2022, which is utter nonsense. At present, one of my postdoc colleagues from my former lab is trying to privately publish our findings. Another lab in California that had participated in the isolation study was also raided in the same time frame as our lab.

• There is no virus called SARS-CoV 2 (I’ve just proven this with the most accurate scientific methodology of isolation and purification, using their own techniques and GOLD STANDARDS) that causes Covid 19. Hence there is no Covid 19, no variants, no Gamma variant, no Delta variant, no Omicron variant, no Monkeypox virus (is however a direct effect of the Covid jab, not a new virus), or any of the other crap, and BS they’re trying to shove down your throat.

• Their own criteria of isolation and purification done the wrong way implicates them. Not only that, they’ve FAILED MISERABLY to meet the 4 Koch’s Postulates and their own “modifications” of the River’s Criteria.

• And last but not least, they’ve done such a shoddy job of the “In Silico” (computer generated) SARS CoV 2 genome that even conventional Indian researchers in February 2020, found suspicious HIV spike proteins in the genome, and were consequently forced to retract their really fantastic paper. How do you find HIV spike proteins in a “NOVEL” virus genome” You don’t folks. It’s called FRAUD. It was made up on the Computer.
  
  The WRONG and FRAUDULENT way to Isolate and Purify a Virus …..

Virologists have been de-frauding all of science since 1952 thanks to virologist John Enders and his FRAUDULENT Polio virus isolation technique.
This is how THEY do it…for Covid 19 as well…

• 1. Get a sample of lung fluid (from a process called aspiration) from a patient who has tested positive for Covid through the BOUGUS PCR test

• 2. Mix the lung fluid in FOREIGN TISSUE cultures of INFECTED Monkey kidney cells called Vero 6 cells they obtained from a Black woman by the name of Henrietta Lacks in the 1950s from her tumor, hence the name: HeLa)

• 3. Then add to this mix, toxic antibiotics such as Gentamicin, Amphotericin B, Vancomycin, and sometimes an anti-fungal like an azole drug

• 4. Then to this mix they further add foreign proteolytic (protein dissolving) enzymes like trypsin, plus bovine calf serum as food for the cell culture.

• 5. Then this toxic mess is left to hang around in a petri dish for up to a week during which time, the toxic soup starts disintegrating and the original human lung cells start breaking apart as they are being starved (as they are now outside the body), poisoned by the antibiotics, the antifungals, the infected monkey kidney cells and the cancer cells that were added in there. The trypsin starts to erode to the protein layer from cells and the calf serum was used as temporary food for the lung cells otherwise they would die within hours. What is observed by these virologists at this point is that the POISONED HUMAN LUNG CELLS are breaking down completely and they observe these tiny tiny particles coming out of the BROKEN DOWN HUMAN LUNG CELL WALLS under a scanning electron microscope at x12.000 magnification. These tiny particles which are human cellular debris, are what virologists “fraudulently” call VIRUSES.

• 6. Once they observe these tiny particles come out of the poor poisoned cell, they immediately name it a virus. No further biochemical tests are done to see what the chemical composition of these tiny particles is: by the logic of a 6-year-old, we can conclude that the CYTOPATHIC effects (fancy word for cell poisoning residue, fungal residue, cancer cell residue, calf bovine serum residue, pretty much anything EXCEPT AN ISOLATED VIRUS.

• 7. To make matters even more anti-scientific, no control studies are run parallel to the isolation procedure described above. This toxic soup is then injected into a poor animal like a mouse or ferret to see the effects on the animal. If the animal dies, they say the virus caused the death, hence the virus is DEADLY. By what logic is this ISOLATION OR PURIFICATION FOLKS? No it is not, it is pure FRAUD.
  

  The 5 FRAUDULENT Papers that Supposedly Isolated and Purified SARS CoV 2:
  . The Five references to initial ANTI- scientifically peer-reviewed papers that started escalating this FRAUD are as follows doing the isolation and purification the WRONG WAY. Please see the methodology sections of each paper.

• 1. Zhou, P., Yang, XI.., Wang, XG. Et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature 579, 270-273 (2020), (here)

• 2. Na Zhu et al. A Novel Coronavirus from Patients with Pneumonia in China, 2019. N Engl J Med 2020: 382:727-733 (here)

• 3. Jeon-Min Kim et al. Identification of Coronavirus Isolated from a Patient in Korea with COVID-19. Osong Public Health Res Perspect 2020;11(1):3-7. (here)

• 4. Drosten et al. Diagnostic detection of 2019 nCoV by real-time RT-PCR. 2020; 1-13. (here)

• 5. McMaster University, Canada: The Correct and Scientific Way of Isolation, Purification, and Characterization: (here)

• Prior to 1952 and John Enders and his Polio virus isolation and vaccine fraud, virology was somewhat of a SOBER field, and I say this very very cautiously. Only my lab and 6 other labs that I personally know of in the United States or anywhere else on the planet have isolated, purified, and characterized the lung fluids of supposed “Covid positive” patients in the CORRECT SCIENTIFIC METHODOLOGY, which I will describe below”
  The CORRECT and SCIENTIFIC methodology to ISOLATE AND PURIFY a Virus or any germ for that matter:

• 1. Extract the lung fluid from a patient through aspiration, who has tested positive for COVID-19 with or WITHOUT the BOGUS PCR test. Our lab had already acquired the COVID-19-positive sample beforehand in a large batch of 1500 samples from Southern California, so we did not have to perform the lung aspirations.

• 2. The UNCONTAMINATED lung fluid is put through either a gravity filtration process with filtration papers that are “qualitative” in nature (meaning having very small pores, so that larger particles are trapped in the filter paper, while the smallest particles end up in the borosilicate flask at the bottom in the liquid collected called the filtrate), or a vacuum filtration process. The vacuum filtration process is faster as a vacuum is used to filter out all impurities such as larger particles such as cellular debris, bacteria, fungi, etc., leaving only the smallest particles.

• 3. The filtrate collected in the flask is then run through the density gradient centrifugation process, whereby the filtrate is poured into a test tube along with silicon beads and either a sucrose (sugar) based or cesium chloride-based solution. The whole test tube is then spun at very high speeds to separate out the microorganism or “virus” in this case. We see several density layer bands forming in the test tube after the centrifugation process, and the layer that is considered isolated as virus particles at a density of 1.16 ng/l is then micro-pipetted out onto a sterile petri dish using an instrument called a micro-pipetter.

• 4. Once you micropipette the “viral” particles onto a sterile petri dish, they need to be bio-chemically analyzed and genetically sequenced either through a process called Sanger sequencing or a DNA extraction process called Maxam Gilbert DNA sequencing. The particles should also be seen under a scanning electron microscope to make sure they are of uniform size, shape, and structure. This whole process is called the isolation, purification, and characterization of a microorganism.

• 5. There is the next step of causation studies which is the GOLD STANDARD of this entire protocol. The causation method is where you have to prove without a shadow of doubt that the extracted and genetically sequenced particles above CAUSE THE EXACT SAME SYMPTOMS, not similar, but exact symptoms in a healthy animal, as is seen in the original diseased host, which can be any animal or human. This causation study is done via a methodology called the 4 Koch’s Postulates.

• The “Henle-Koch” postulates: First formulated by the German pathologist Friedrich Gustav Jacob Henle (1809 – 1885) and adapted and modified by his pupil the German bacteriologist Robert Koch (1843 – 1910), these are four criteria that are the “gold standard procedure” to confirm the causal relationship of a pathogenic organism to a specific infectious disease.
  The 4 postulates are: (here)

• 1. The microorganism must be found in abundance in all organisms suffering from 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 re-isolated from the inoculated, diseased experimental host and identified as being identical to the original specific causative agent.
  

  The CORRECT and SCIENTIFIC Way of Isolation, Purification and Characterization:

• In addition to the GOLD STANDARD of the 4 Koch’s Postulates in proving that the microorganism was the one causing the DISEASE, we also have to conduct CONTROL studies, where mice or ferrets are injected with a saline solution. Virologists in labs all over the world always conveniently forget the control studies in conjunction with the sham isolation, purification, characterization, and causation studies they routinely conduct.

• A correctly and scientifically isolated and purified virus should have an INTACT genome of between 30,000 to 40,000 base pairs, NOT the 40 base pairs the Wuhan scientists purportedly found which they called the “NOVEL”. There are 4 base pairs, also called nucleic acids, these are: Adenine (A), Thymine (T), Cytosine (C), and Guanine (G). Adenine always pairs with Thymine and Cytosine always pairs with Guanine. In RNA viruses such as the SARS CoV 2 coronavirus, the Thymine is replaced by a nucleic acid called Uracil.
  Virology, Added Insult to Injury, Part 2: River’s Criteria Circa 1937:
  More fraud from virologists….cannot meet Koch’s Postulates, so they modify them. They came up with something called River’s Criteria in 1937.
  These postulates were proposed by Thomas M. River in 1937 to establish the role of a specific virus as the cause of a specific disease. These postulates are the modifications of Koch’s postulates.

• 1. The viral agent must be found either in the host’s (animal or plant) body fluids at the time of disease or in cells showing lesions specific to that disease.

  2. The host material with the viral agent used to inoculate a healthy host (test organism) must be free of any other microorganism.

  3. The viral agent obtained from the infected host must Produce the specific disease in a suitable healthy host, and/or Provide evidence of infection by inducing the formation of antibodies specific to that agent.

  4. Similar material (viral particle) from the newly infected host (test organism) must be isolated and capable of transmitting the specific disease to other healthy hosts.
  VIRUSES – INTRODUCTION, MORPHOLOGY, CLASSIFICATION & RIVER’s POSTULATES (here)

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