Creating the “Coronavirus”

I think it’s simple logic. It doesn’t require that anyone have any specialized knowledge of the field. The fact is that if there were evidence that HIV causes AIDS-if anyone who was in fact a specialist in that area could write a review of the literature, in which a number of scientific studies were cited that either singly or as a group could support the hypothesis that HIV is the probable cause of AIDS-somebody would have written it. There’s no paper, nor is there a review mentioning a number of papers that all taken together would support that statement. -Kary Mullis

One of the best pieces of advice I took from the late Kary Mullis, inventor of the PCR technology currently being abused today, is that it is always important to go back and find the original source for any given claim. While the above quote is about HIV and AIDS, the logical reasoning can be applied to any “virus” past and present. What does the evidence show? If a claim is made, where and how was it established? What do the little numbers cited in each paper actually lead us to and tell us? If a novel “virus” is going to be built upon the back of the unrelated work of others over numerous decades, then those original studies should have the evidence neccessary to back up the claims made by current ones.

With the rise of “SARS-COV-2,” many claims were made about a novel “virus” and it’s supposed relation morphologically, serologically, and genetically to previous “coronaviruses” discovered over the past 60 years. While it would be easy to let these statements stand as is, when the very existence of the “virus” associated with our current “pandemic” hinges on the accuracy and validity of the work of previous researchers, these claims demand extra attention and research. In the case of the “coronaviruses,” this meant tracking down every original paper alleging the existence of any strain of this “virus” and scrutinizing the evidence presented. It also meant, in many cases, relying on the citations provided in these early papers in order to expand upon what was there and to elucidate the information that was missing.

Fortunately, when you read one “virus” paper, you have essentially read them all. Nearly every study can be broken down into the proceeding steps outlined below. Some papers will contain all of these steps while others may only utilize one or two of them but this is a general overview into the creation of a “coronavirus” (or any “virus” for that matter).

Step One: Take a sample directly from a patient and add it to transport medium without purifying any particles first.

After going through the original papers used as proof for the existence of “Coronaviruses,” it was obvious that not once during the 60 years of existence were any of these supposed “viruses”ever properly purified (i.e. made free of any contaminants, pollutants, foreign materials) nor isolated (i.e. separated from everything else) directly from samples taken from sick humans. The methods used for purification/isolation include ultracentrifugation, filtration, and precipitation. These steps are absolutely essential as if purification/isolation is not done, the particles assumed to be “viruses” will be in samples containing potentially millions of similar or identical ones. If these steps are ignored, there can be no independent variable (i.e. isolated particles assumed to be “viruses”) that can be used and manipulated in order to prove that the particles alone are the cause of disease. What one will find upon reading any of these papers is that the unpurified sample (which contains many microbes and particles other than assumed “virus”) is immediately placed in some form of “viral” transport medium containing various additives/chemicals, thus immediately defeating any claims of purification/isolation.

Step 2: Mix the unpurified sample into a culture containing added ingredients.

The sample is always added to a culture system, whether it is tissue, organ, or cell culture. The culture will contain many added compounds, chemicals, and ingredients such as fetal bovine serum, antibiotics/antifungals, and growth media made up of various “nutrients.” These cultured cocktails are incubated for days and often the added ingredients are discarded and replenished at regular intervals. The “viruses” are either passaged by taking the culture supernatant (the top layer) and adding it to fresh cells or, as done back in the old days, the supernatant is injected intracranially into animals (such as ferrets and/or mice) which will have their own brains emulsified into a new culture.

Step 3: Look for cell damage in order to claim a “virus” is present in the sample.

This toxic mixture of unpurified human and animal remains is where the claimed “virus” resides. It is never seen directly and only assumed to exist due to indirect cytopathogenic effects (CPE) noted in the culture. The CPE is cell damage that is said to be the result of the “virus” even though there are numerous other explanations for why this effect occurs such as contamination, the use of antibiotics/antifungals, or even as a direct result of passaging the culture itself. If this CPE is seen, the culture process is considered a success and it is assumed a “virus” has grown.

Step 4: Use the unpurified culture supernatant to take EM images in order to find a representative “viral” particle from among many similar ones.

This unpurified goo is often subjected to further alterations such as fixing, embedding, and staining in order to be visualized under the electron microscope. This process kills any “living” components and can create artificial artefacts which are often claimed to be “viruses.” Virologists will look through the goo to find particles which fit their preconceived notion of what their “viris” particle should look like and claim it as the culprit even though there are potentially millions of other similar or identical candidates within the unpurified cultured supernatant. In fact, it is admitted that there are various similar looking particles such as clathrin-coated vesicles, secretory vesicles and granules, exosomes, and other multivesicular bodies within these samples which are commonly mistaken for “coronaviruses.”

Step 5: Perform various indirect non-specific serological tests in order to claim the “virus” is new but related to other “viruses.”

Another indirect method utilized for claiming that these “viruses” exist within the culture supernatant include antibody testing. Serological tests such as complement fixation, haemagglutination inhibition, and neutralization tests are commonly performed. These supposedly “virus-specific” results are used to classify one strain over another as well as determine immunological information. However, there are a few problems with these methods. The first is that the tests are regularly non-specific and cross-react with other “viruses.” The results are regularly difficult to reproduce and replicate which has led to a reproducibility crisis. The second, and far bigger problem, is that like “viruses,” antibodies have never been purified/isolated directly from humans and are an entirely unproven theoretical concept with assigned functions that have never been observed. One can not use non-specific results indicating reactions of theoretical particles (antibodies) to identify the existence of other theoretical particles (“viruses”).

Step 6: Create a genome from the unpurified sample or culture supernatant and develop diagnostic tests based on these random fragments of A,C,T,G’s.

With the rise of genomics and molecular virology came another indirect method utilized as proof for the existence of “viruses:” the “viral” genome. Using various technologies like Sanger sequencing, next-generation sequencing, metagenomics, PCR reactions, computer algorithms, alignment software, reference genomes, etc., virologists have created a database full of random A,C,T,G’s said to represent these invisible particles. Diagnostic tests are then created to search for these computer-generated fragments. However, nearly every genome is taken from the unpurified cell culture supernatants which contain DNA/RNA from various known and unknown sources. If not taken from cell cultures, the RNA/DNA is taken directly from unpurified samples such as bronchoalveolar lavage fluid as in the creation of the “SARS-COV-2” genome. These genomes are then built on the backs of reference genomes which were created in the same way using unpurified sources. At no point in the chain of “coronaviruses” from the 1960’s to today has there ever been a genome taken from purified/isolated particles. Thus, there can be no certainty that any of the RNA claimed to belong to a “viral” genome is in fact “viral” as it could have come from numerous sources such as the host cell, the fetal bovine serum, exosomes or other MVB’s, contaminants, bacteria, etc.

The “Coronavirus” Papers

Presented below are all of the original human “coronavirus” papers for each strain given in chronological order. I broke down and summarized the papers and provided some extra history and/or method information where necessary. While I provided the full papers for the older “coronaviruses,” the newer papers are much longer so I highlighted the important sections. Every paper is linked within so my breakdown/commentary can be skipped if it is desired just to read the original studies for themselves. In the case of the older (and also for some newer) papers, the DOI # is the only way to access the full study. To do so, copy the DOI # at the end of each study breakdown, go to, and then paste the DOI to search for and open or download the paper. I have given a brief overview on the creation of each strain here as well. You should be able to see the 6 steps outlined above and the general pattern used for the creation of the “coronaviruses.”

B814 (1965)

B814 is the original human strain of the “coronavirus” discovered by D.A. Tyrrell in the early 1960’s. Nasal washings were immediately stored in phosphate-buffered saline and bacteriological nutrient broth. The washings were then transferred into organ cultures of 14 to 22 week old fetuses mixed with Medium 199 and sodium bicarbonate. The medium was changed daily for two days and after about ten days, some were fixed in Bouin’s solution, embedded, sectioned, and stained with haematoxylin and eosin. Haemagglutination-inhibition tests were performed to determine serological information for an unknown “virus.” Cold symptoms were only produced in volunteers given the nasal washings with the addition of demethylchlortetracycline. No EM images of purified particles accompanied the study. This initial version of the “coronavirus” mysteriously disappeared in the early 1970’s.

229E (1966)

229E is considered the first human “coronavirus” even though the forgotten B814 was “discovered” a few years prior. This version was found by Dorothy Hamre after she  took samples from 5 individuals (four who were unhealthy and one who was healthy) and subjected them to human kidney cultures. “Virus” could only be produced after the second blind passage. These “viruses” only produced CPE in human diploid cell strains taken from aborted fetuses and only these cultures, HEL or WI-38, were used for all further experiments. Non-specific complement fixation and neutralization tests were utilized to determine “specific” antibody responses for the unseen “virus.” No EM images accompanied Hamre’s initial paper. The 2012 genome for 229E was taken from an unpurified culture and built from the reference of a synthetic lab-created recombinant HCoV-229E cDNA clone (Inf-1) from 2001 that was based on the 1973-deposited laboratory-adapted prototype strain of HCoV-229E (VR-740).

Imaging the “Coronaviruses” (1967)

In this 1967 paper by June Almeida, which she co-authored with D.A. Tyrrell, Almeida claimed to use a new negative staining approach for her electron microscope images on unpurified samples in order to characterize the three uncharacterized “viruses.” She found particles in the unpurified culture supernatant that resembled influenza as well as Avian Infectious Bronchitis and Murine Hepatitis “Virus.” Her initial findings were rejected on peer review because the referees said the images she had produced were just bad pictures of influenza “virus” particles. Almeida’s images were eventually published as “coronaviruses” two years later even though skepticism remained.

OC43 (1967)

The second official strain of the “coronavirus” is OC43 which was discovered by Kenneth McIntosh in 1967. This process was broken into two parts. His first paper tested nasopharyngeal wash fluid which was inoculated into each of two tubes of the following tissue cultures: HEp-2, primary human embryonic kidney, rhesus monkey kidney, and human diploid cell strains (HDCS) WI-26, WI-38, and AT-39. These cultures were observed for the customary CPE and any samples which did not display this effect were further studied using human embryonic tracheal organ cultures. Tracheas were obtained from fetuses spontaneously aborted at 5-9 months’ gestational age. The tissue was excised en bloc by sterile technique and immediately stored in cold Hanks’ balanced salt solution with 10% fetal calf serum, 250 u/ml penicillin, and 250 u/ml streptomycin. Tissue fragments were made which were were partially covered with 1.25 ml of Leibovitz medium, supplemented with 0.2% bovine albumin, 0.1 mM glutamine, 250 u/ml penicillin, and 250 u/ml streptomycin. Standard serologic tests were performed and EM images were obtained from unpurified culture supernatant.

In his second paper, McIntosh attempted to “adapt” his “virus” to suckling mice as he was unable to grow his “virus” using the standard tissue culture techniques. He chose suckling mice as he knew he could find the same particles in mice as those discovered by Almeida, Tyrrell, and Hamre since the murine hepatitis “virus” was morphologically identical. Suspensions used for mouse inoculation were prepared from material passaged four to five times in organ culture and contained “IBV-like virus” particles when examined by electron microscopy after tenfold concentration. Suckling mouse passages were performed either by combined intracranial (IC) and intraperitoneal (IP) inoculation or by the IC route alone. From these experiments, he determined that one mouse, designated OC43, contained the “virus” he was searching for.

It wasn’t until 2005 that a genome for OC43 came about from a prototype HCoV-OC43 strain (ATCC VR759) which was a laboratory strain that, since its “isolation” in 1967, had been passaged 7 times in human embryonic tracheal organ culture, followed by 15 passages in suckling mouse brain cells and an unknown number of passages in human rectal tumor HRT-18 cells and/or Vero cells. It was then further cultured in the human rhabdomyosarcoma (RD) cell line which is derived from the most common soft tissue sarcoma of childhood and adolescence. The RD cell line used for the OC43 genome came directly from biopsy specimens of a 7-year-old female with a pelvic RMS previously treated with cyclophosphamide and radiation and found to have refractory disease. It is grown in Eagle’s Medium with 10% fetal bovine serum. This unpurified concoction was used along with reference genomes primarily from bovine and murine “coronaviruses” in order to build the OC43 genome.

Naming the “Coronaviruses” (1968)

In 1968, eight virologists (including Tyrrell, Hamre, Almeida, and McIntosh) wrote the announcement of a new family of “viruses” in the journal Nature. They claimed that the particles they all recovered from tissue and organ cultures in humans were different strains of the same “virus” which just so happened to resembls those found in chickens and mice. The researchers relied on negative staining in electron microscopes and used several indirect methods such as complement fixation, neutralization tests, hemadsorption, etc. in order to detect these “viruses.” They claimed that these particles, despite some polymorphism (i.e. two or more clearly different types exist in the same population of the same species; more than one form or morph) all had a characteristic fringe of projections which they felt resembled a solar corona, hence the name “Corona-virus.” The main strains identified in the announcement were B814, 229E, and OC43. Oddly enough, B814 would disappear forever less than a decade after its “discovery” while 229E and OC43 would go unchallenged as the only “coronaviruses” for over 30 years until the dawn of molecular virology and the creation of “SARS-COV-1” in 2003.

SARS-COV-1 (2003)

In 2003, the third human “coronavirus” was discovered by multiple researchers. Their papers will all be presented below. From the initial paper by Peiris, “viruses” were “isolated” on fetal rhesus kidney cells from the lung biopsy and nasopharyngeal aspirate of two patients. The initial cytopathic effect noted was the appearance of rounded refractile cells appearing 2–4 days after inoculation. The cytopathic effect did not progress in the initial culture tubes but on subsequent passage, and appeared in 24 h. Of 30 cloned RT-PCR samples from one of the patients, only one 646 bp fragment of unknown origin showing weak homology to “coronaviruses” was found and this was subsequently used to create RT-PCR assays for diagnosis. Of the 44 nasopharyngeal samples available from the 50 “SARS” patients, only 22 had evidence of human pneumonia-associated “coronavirus” RNA. Five patients had no virological evidence of “SARS” whatsoever yet they were still considered “SARS” cases. Other pathogens were found in some of the patients but these were relegated to possible secondary invaders. The usual serological tests and EM images were done on the unpurified samples.

NL63 (2004)

In 2004, Lia Van Der Hoek created the fourth official “coronavirus” in NL63. To do so, she relied upon the use of her own unproven method called VIDISCA. Papers like this highlight the fatal flaws currently dominating virology which is the over reliance on molecular tests and data as proof of “virus” discovery. Van Der Hoek claimed her method can sequence the genome of an unknown “virus.” The problem is that this sequence did not come from purified/isolated particles. It came directly from unpurified monkey kidney cell culture supernatant that was mixed with the nasopharyngeal aspirate from a 7-month old baby. As described by Van Der Hoek, the clinical sample was subsequently inoculated onto human fetal lung fibroblasts, tertiary monkey kidney cells (Cynomolgus monkey) and HeLa cells. CPE was detected exclusively on tertiary monkey kidney cells, and was first noted 8 d after inoculation. More pronounced CPE was observed upon passage onto the monkey kidney cell line LLC-MK2 while additional subcultures on human fetal lung fibroblasts, rhabdomyosarcoma cells and Vero cells remained negative for CPE. The supernatant of the CPE-positive LLC-MK2 culture NL63 was then analyzed by VIDISCA in order to create the genome. No serological test results nor any EM images of particles said to be NL63 were presented in the study.

HKU1 (2005)

In 2005, Patrick Woo isolated what he claimed was the fifth new “coronavirus” from one 71-year-old patient. Isolation of the “virus” by using various cell lines, mixed neuron-glia culture, and intracerebral inoculation of suckling mice were all unsuccessful. Thus, the only evidence Woo could present was a genome stitched together from RT-PCR primers designed by multiple alignment of the nucleotide sequences of available pol genes of known “coronaviruses.” The RNA used came from unpurified nasopharyngeal aspirates, feces, and urine. The complete genome came from the unpurified NPA’s and the cDNA was amplified by degenerate primers designed by multiple alignment of the genomes of murine hepatitis “virus” (MHV), HCoV-OC43, bovine “coronavirus” (BCoV), rat sialodacryoadenitis “coronavirus” (SDAV), equine “coronavirus” NC99 (ECoV), and porcine hemagglutinating encephalomyelitis “virus” (PHEV). Sequences were assembled and manually edited to produce a final sequence of the “viral” genome. Woo could not culture his “virus” nor show proof of pathogenicity even after intracranial inoculation in suckling mice. He had no specific antibodies and no evidence of transmissibility. There was no evidence for disease prevalence and he lacked a large sample size. No EM images of particles assumed to be NL63 exist.

MERS (2012)

In 2012, the sixth human “coronavirus” was discovered by Dr. Ali Mohamed Zaki in Saudi Arabia. Blood samples were taken from a 60-year-old Saudi man who was admitted to a private hospital in Jeddah, Saudi Arabia, on June 13, 2012, with a 7-day history of fever, cough, expectoration, and shortness of breath. The samples were mixed with “viral” transport media and the supernatant was used to inoculate Vero and LLC-MK2 cells by adsorption for 1 hour at room temperature, after which 2% fetal bovine serum in minimal essential medium Eagle was added. A genome was created from the unpurified supernatant and aligned to reference genomes of previous “coronaviruses.” Non-specific IgG antibody results were obtained while IgM was not tested. Genomic analysis was used to create a relationship to other “coronaviruses.” No EM images of particles claimed to be MERS were presented.

SARS-COV-2 (2019)

At the tail end of 2019, the seventh (but definitely not final by the looks of things) “coronavirus” was created with “SARS-COV-2.” There were many papers used to claim the isolation of a novel “coronavirus” yet all of them failed at providing evidence of purification/isolation of any “virus.” In fact, four of the main papers (Zhu, Park, Kim, Poon) admitted to not purifying their “viruses” while both Zhou and Zhu admitted to not fulfilling Koch’s Postulates, four absolutely essential logical criteria needed to be fulfilled in order to claim a new pathogen exists.

According to the Zhou paper, the earliest of those published, five samples from sick patients were found to be PCR-positive for CoVs. One sample (WIV04), collected from the bronchoalveolar lavage fluid (BALF), was analysed by metagenomics analysis using next-generation sequencing to identify potential aetiological agents. By de novo assembly and targeted PCR, they obtained a 29,891-base-pair CoV genome that shared 79.6% sequence identity to SARS-CoV-1. High genome coverage was obtained by remapping the total reads to this genome. By genomic analysis, they matched it to bat “coronavirus” RaTG13 with an overall genome sequence identity of 96.2%. They didn’t attempt “isolation” of a “virus” until after the genome was created from unpurified BALF. The isolation consisted of NP swabs which were mixed with 1.5 ml DMEM containing 2% FBS. The “viral” transport medium was composed of Hank’s balanced salt solution (pH 7.4) containing BSA (1%), amphotericin (15 μg ml-1), penicillin G (100 units ml-1) and streptomycin (50 μg ml-1). Vero E6 and Huh7 cells, which were cultured in DMEM containing 10% FBS, were used to culture the “virus.” The culture was subjected to many other chemicals and additives throughout the “isolation” process. No EM images accompanied the study even though they were mentioned as being done.

The Zhou paper and a few others are presented below. You will find similar procedures and unscientific results in all of the “SARS-COV-2” papers. However, you will not find purified/isolated particles taken directly from humans and subsequently proven pathogenic in a natural way.

Breaking the Chain

It is very clear that from B814 in 1965 to “SARS-COV-2” in 2019, not a single one of these “coronaviruses” was ever properly purified and isolated directly from a sick host and proven pathogenic in a natural way. This means that none of the EM images plastered in the media to generate fear should hold any power as the representative particles could be anything, including inert artificial creations derived from the very processes said to grow and image them. The supposedly specific antibody results should be ignored as without having purified/isolated the “virus” first, specific antibodies can not be determined. The “viral” genome should be thrown out as the RNA/DNA can and does come from numerous sources both known and unknown. The “viral” RNA has never been shown to come from any purified/isolated “virus” past or present. The PCR diagnosis should be seen for what it truly is, an absolutely inaccurate, easily manipulated, and meaningless measurement being abused to label a person with a “viral” sequence never proven to come from particles that exist in reality.

Every measurement used as proof for the existence of the “coronaviruses” stems from indirect evidence acquired through unscientific and grotesque experimentation with conclusions drawn that defy logic and reasoning. There never has been any direct evidence for the existence of this or any other “virus.” The history of the “coronavirus” is a flimsy yet carefully crafted narrative that falls apart upon critical examination. It’s time to lift the veil on this generational scam for everyone to see so that this cycle of madness can end once and for all.



  1. Extraordinary piece. You are providing an incredible service to the world. This one article exposes the questionable science of virology is a very easy to read format. You are making a difference. Forever grateful for all that you do. Thank you.

    Liked by 1 person

    1. Thank you so much for the encouragement and support! It is nice to hear that the article is easy to read. I try not to get overly technical but sometimes it can be difficult to explain their fiction easily. I will continue to do my part to expose the lies and corruption. Thanks again 🙂


  2. Thank you, thank you, thank you from the bottom of my heart. The information on your web page is beyond awesome. I was questioning things from the beginning and re-questioning everything. You are the answer to all my searching. Going to pass this on to my friends.

    Liked by 1 person

  3. This all goes back to Pasteur’s need to create a reason for supposedly curing disease, which he admits later was faked. Stefan Lanka says it goes back further to Virchow who also fabricated the idea of cell theory.
    There are 2 vital questions which arise from this medical fraud, firstly what are the real causes of disease being deflected by germ theory? And then to understand how disease is really the absence of something called health which occurs when one fails to take sufficient measures to maintain good health. This is really what the medical estaishment wants to ignore because then they’d be out of a job!

    Liked by 3 people

    1. Yes, the pharmaceutical industry does not want to cure anything. They want us in a perpetual state of disease in order to profit from us and keep us weak and under control. They have gone to great lengths to cover up the truth about health and disease. Fortunately, people like Dr. Lanka have done an amazing job exposing their lies. I am greatly indebted to them all for helping to open my own eyes.

      Liked by 3 people

  4. Without your website, I very well might still be a “covid” believer.
    I cannot appreciate enough that you have answered all of my questions (so far) about this.
    This whole “covid” cult, I don’t wish that God “spare” them, because they *choose* to believe.

    Liked by 1 person

    1. Thanks for the kind words! It is sad as we have all been indoctrinated from birth to believe in this lie.. Critical thought and logical thinking has been destroyed by an educational system hellbent on drilling memorization and repetition into the mind. There is a difficult cognitive dissonance that must be broken in order for one to be honest and accept that we have been lied to about many things throughout our lives by those who are in charge. While I emphasize with the “Covid” cult to an extent, there is no excuse anymore in this day and age to remain blissfully ignorant. The information is literally at our fingertips. All we have to do is take the time to do a little research, reading, and thinking. Many of us are sounding the alarm while being ignored. My empathy runs out when people are given the truth yet choose to return to the lie. I am happy to hear that you have found this information beneficial! 🙂

      Liked by 1 person

  5. At my public concentration camp (often called a “school”), in my “science” class, I don’t remember the scientific method being mentioned at all. Maybe I forgot, but if so, it (the scientific method) has been emphasized VERY little in this “class.” Mostly it’s just memorizing unproven declarations. I also don’t empathize too much, even for the 13 and 14 year olds who believe the baseless declarations, because I think even they are mature enough to use rationality and logic.

    Liked by 1 person

    1. The scientific method is definitely not emphasized. They somewhat mentioned it in my science class yet it was not concentrated on. As you said, memorization was the focus while critical thought was lost.


    1. Thanks, I appreciate the kind words and support! At this point in time, I’m not looking to debate anyone as I am very much focused on using my free time to update all of my old FB research posts onto this blog (before they delete them) and doing new research/posts. I’ve had “debates” with microbiologists before on FB and they can never get past the initial lack of evidence for any purified/isolated “virus” directly from a human sample and then proven pathogenic in a natural way. It normally devolves into an attack of ad homenums, appeals to credentials/authority, and appeals to consensus. I learned long ago nothing ever comes from these debates as they devolve rather quickly. If any microbiologist/virologist can actually find and share the evidence of a purified/isolated “virus” directly from a human sample and proven pathogenic in a natural way, then I would be willing to listen and talk. This has never happened in any conversation I’ve had with them nor has it occurred in any of my friends conversations when they have engaged with them.


      1. I only did a quick read but it doesn’t look like purification nor isolation is claimed at all. They are just taking unpurified fluid and looking for particles in a microscope.


      2. I totally get where you’re coming from. Public debates do have the benefit of affording the recipient of the information the opportunity to see people from different camps hash things out on one platform. But I totally get your point. In any case, what do you think about Dr. Wilson’s argument (in the video I sent you) that Cryelectron microscopy can be used to qualify the existence of viruses in ways that conventional electron microscopy can’t, without the need for viral purification?

        Sent from my iPhone



      3. He needs to first show purified/isolated particles taken directly from humans for whichever “virus” he claims exists. This should be shown in the original publication claiming the existence of said “virus.” Only then can cryo electron microscopy have any value if used on the purified/isolated sample. Even then, that would only prove these particles exist, not that they are pathogenic. He and others are so quick to jump to newer imaging technology as proof of “viruses” when the original papers never proved “viruses” exist to begin with. Showing images of particles claimed to be “viruses” does not prove nor make them “viruses.”


    1. That is a very good suggestion. I tried digging into it in the past but it is a complicated one to unravel. That was why I focused on the complete lack of purified/isolated “coronaviruses.” Without a “coronavirus,” there is no spike protein. Or at least not the way in which they want us to believe anyways.


    2. A short video, includes transcript.'The-Spike-protein-doesn't-exist'—ORWELL-CITY:a6052a32a9191f0a96c26c839efb8823a0c7947b?src=embed

      There was a post on Corona_Fakten

      Google translate.

      There are no viral spike proteins. It is and will remain a misinterpretation

      ✅ ACE-2 was found in 2000; ACE-2 is practically absent from the upper airways. In 2003 it was claimed ad hoc, without any evidence, that this enzyme was the receptor for corona viruses in the lungs.

      ✅The substrate for this enzyme is a protein, which is formed in high concentrations when the egg cell nests and the placenta is formed, i.e. it plays a role.
      This protein was previously interpreted into the model of the corona virus as a spike protein.
      In other words: ACE-2 is the receptor to which the “spike protein” attaches.
      In 2000 the “ACE-2” receptor was found. When coronaviruses were then claimed in 2003, which have not yet been scientifically proven, the protein that was discovered when docking to the ACE-2 was mistakenly declared as a virus protein, despite the fact that it was in the lungs this receptor does not even occur.

      ✅It is only a model, in reality there is a similar protein whose function is not known and the fear that the vaccination could affect this real protein is unjustified, since the immune models together with the cell theory are without exception refuted.
      Note🙋‍♂️: The protein that normally exists in the body, which is passed off as a viral protein, has been changed significantly by “virologists” in the sequence in order to sell it as a viral protein.
      In the real nature of humans, however, this does not exist, only a construct is shown.
      👉 Dr. Tipnis – A human homolog of angiotensin-converting enzyme. Cloning and functional expression as a captopril-insensitive carboxypeptidase
      👉 Power plant – entry into the refutation of the virus claim
      👉 Virus misinterpretation – how genome analysis creates fictitious viruses

      The exosomes part is also confusing .
      My understanding is they are chunk separating from tissues that can be seen in reality but misinterpreted as having a role so is misleading and confusing the notion that ‘viruses ‘ may be some form of exosomes.

      Google translate

      The exosome theory is just an auxiliary hypothesis ❗️

      💡The exosomes – why this auxiliary hypothesis is misleading from the whole point of view

      ✅ Within the cell theory (refuted) the decay of isolated chunks of tissue, are interpreted as cells, but also connective tissue-containing excretions of humans / animals are interpreted as “exosomes”.

      ✅ The disadvantage of this theory is that those involved and the recipients (i.e. you) of this information believe that the virologists have found something specific that would point to something (illness, excretion, 5G and the devil etc.).

      ✅ This inadvertently distracts from the fact that no specific RNA or other molecules are detected at all, but rather these can only be put mentally together to form a whole, for which from year 1952 the phages, the supposed viruses of the bacteria were the inspiration.

      In summary, exosomes:

      ✅ These structures, which are claimed to be viruses and are now being tried by others to interpret as harmless but specific structures (exosomes), do not correspond to the facts.
      Because DNA / RNA is constantly changing.

      ✅The fictitious construction of genome strands using a process such as sequence alignment and sequence assembly (stringing together many short RNA sequences) does not in any way reflect reality.


      💡 Harold Hillman & Gilbert N. Ling- The Artifacts of the EM Recordings & Refutation of the Cell Theory

      ✅ Although it was first discovered decades ago in the heart muscle and due to ever better observation techniques with which one has to manipulate the tissue to be viewed less and less, it is clear to everyone involved that tissue densities, which were interpreted as cells, are so intensely connected to one another via their gel-like substance are that they can only be called cells if the logic and terminology are disregarded.

      ✅ Since 1978, a group of scientists around the neurologist Harold Hillmann has continuously researched and published the facts in scientific journals, at congresses and in book form, why and how the changes in dying, mechanical dissection, chemical fixing and dyeing of tissue – in order to be able to make it visible under the microscope – the invisible, gel-like tissue only looks as if it is organized in definable units.

      ✅ In addition, Harold Hillmann and his colleagues have recognized, proven and published extensively that the electron microscopy (EM) technology created by Virchow’s image of cells is wrong and that EM technology has made a significant contribution to conveying this image and stabilize.

      ✅ Gilbert N. Ling – the liquid in the “cells” is not water

      Summarized EM recordings:
      The only important message to the outside world: only “artifacts” are shown – the key here is:

      1.) that these images only come from cell cultures, i.e. dying tissue in the test tube and definitely do not show anything that comes from a person,

      2.) that these structures have never been characterized biochemically (sic!),

      3.) Nucleic acids that are supposed to be the heart of the virus have never been obtained from these structures (i.e. never from a specific structure that is presented as a virus, the nucleic acid has never been extracted)

      🙋‍♂️A motionless image from electron microscopy never shows the living biological process. What is examined under the EMs has absolutely nothing to do with what happens in the human biological organism. Any result from the laboratory can give absolutely no conclusions about the processes within a living organism.


      👉 Summary refutation of cell theory “W + Magazin Issue 1 -3”

      👉 Literature Harold Hillman

      👉 Virus misinterpretation – how genome analysis creates fictitious viruses

      A reminder what exosomes , based in cellular theory.
      As for their use in therapy sounds like another cash cow for some more elusive therapies

      What are Exosomes?
      Exosomes are so-called extracellular vesicles, or small bubbles, released from cells, especially from stem cells. They act as shuttles for certain genetic information and proteins to other cells.

      They allow for cell-to-cell communication, transporting molecules that are important regulators of intracellular information between close and distant cells. They carry information from place to place with different functions and purposes telling cells how and when to react.

      Exosomes are being heralded as the next frontier of cell therapy.

      While not being cells at all, they play a vital role in the communication and rejuvenation of all the cells in our body. Science has shown that the cell-to cell communication is important in maintaining a healthy cellular terrain.

      Who May Benefit from Exosome Therapy?

      Within the Infusio Concept, exosomes may help regulate processes within the body. Patients with Lyme disease, chronic inflammation, autoimmune disease and other chronic degenerative diseases may benefit from including exosomes in their treatment regimen.

      Exosomes may also be beneficial as part of an anti-aging therapy. Patient with degenerative joint disease have also benefitted from the use of exosomes.”

      So it the elderly with money who will easily fail pray to any promise of anti-aging therapy and anti-ailment treatments.

      Liked by 1 person

  6. Great investigative research.

    A good summary in this article from November 2020, dsalud Spanish team

    During the first half of April, when the first research we conducted indicated that SARS-CoV-2 had not been isolated and since those who claimed to have done so were relying on “isolates” of previous “human coronaviruses”, we began to do a thorough review of those claimed isolates. Specifically, we reviewed the alleged isolation work of suspected human coronaviruses
    -229E (said to have been isolated in 1965),
    -OC43 (in 1967), SARS-CoV (in 2003),
    -NL63 (in 2004),
    -HKU1 (in 2005) and
    -MERSCoV (in 2012).”

    The only thing that has been different between them are the laboratory procedures and techniques that were becoming progressively more sophisticated which, in this case, has implied not a greater accuracy but a greater capacity for deception and self-deception that has culminated in the virtual manufacture of the SARS-CoV-2.”

    Click to access The-scam-has-been-confirmed-Dsalud-November-2020.pdf

    Liked by 1 person

  7. Telegram translate :

    “What does the number of the month mean?

    ✅ Over 1 million fictional non-real virus genomes

    ✅ The genomes contain gene sequences from a mixture of different DNA/RNA, NOT viral

    ✅ The origin of the sequenced gene sequences used cannot be associated due to the lack of an isolate.

    ✅ The necessary control tests have not been carried out for any of these “whole” genome sequencing.

    ✅ Different assembler programs used by the virologists lead to completely different end results with the same raw data.

    ✅ Each new sequencing process (even from the same sample) generates new end results and is falsely sold as a mutation.

    ✅ Any “viral” genome can be constructed from the gene sequences (HIV, measles, hepatitis, etc.)


    🎥 In our video “IQ-Puzzler Pro” from the Beginners series you can understand and check this process based on the authoritative study from China.

    👉 RKI

    deepL translate

    Number of the month
    1,032,194 high-quality whole genome sequences of SARS-CoV-2 from Germany were transmitted to the RKI via DESH

    Modern methods of whole genome sequencing enable the decoding of the entire genetic information of an organism or virus. The sequence of the DNA and RNA building blocks is determined. With today’s technological methods, however, the genetic information often cannot be read out “in one piece”, but only in fragments. Here, bioinformatic algorithms help to put the sequenced fragments in the right order and assemble them into a complete genome sequence.
    Since the genome sequence encodes the blueprint of an organism or virus, it contains information on the resistance and pathogenic properties of a pathogen. If the genetic information changes due to mutations, new virus variants with altered properties can emerge. In order to investigate and understand the effects of newly observed, previously unknown mutations on infectivity, resistance or other properties of the pathogen, further e.g. clinical, epidemiological and experimental data are needed.
    Further information
    German Electronic Sequence Data Hub (DESH)
    Status: 01.09.2022

    Liked by 1 person

    1. An interesting comment.
      deepL translate:

      “Yes, we humans are somewhat limited. When we don’t understand something, we create a model and then claim that this is the reality.
      I never understood why I was drilled into it at school that 1 is 1=2? Today I know that 1 1 is never 2. Because the treatment that 1 is 1=2 is based on a human model. And this model is only correct under one condition, that objects 1 and 1 are 100% identical. And every child knows that there are no 100% identical objects in nature. Long live the diversity of nature and the critical spirit. 😊”


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