January 25, 2021
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David Rasnick , PhD chemist, with a long history working in the pharmaceutical industry (Abbott, Prototek, Arris), broke away from official science and served as the president of Rethinking AIDS: the group for the scientific reappraisal of the HIV hypothesis. He was a member of the Presidential AIDS Advisory Panel of South Africa.
Here is a recent explosive statement Rasnick made  about SARS-CoV-2 and HIV. Digesting it brings about a breakthrough revelation:
“Viruses are unstable, RNA [e.g, SARS-Cov-2] viruses especially. They are so unstable, there is no such thing as an un-mutated RNA virus. They are like snow flakes, no two are identical.”
“HIV is an RNA virus with 9,800 nucleotides. You can download the HIV Sequence Compendium here:” 
“In the Preface it says:”
“’The number of [genetic] sequences in the HIV database is still increasing. In total, at the end of 2017, there were 812,586 sequences in the HIV Sequence Database, an increase of 8.5% since the previous year.”
“None of the sequences of the world destroying [sarcasm], computer generated coronavirus with its 30,000 or so nucleotides, are identical.”
“The virus maniacs use computers to compare the menagerie of sequences to come up with ‘A Consensus Sequence’ for HIV, Coronavirus, and all the rest. The consensus sequence exists in two places: in computers and in strings of RNA synthesized in the lab.”
“Even consensus sequences are not stable. Different groups, using a variety of computer algorithms will invariably come up with different ‘consensus sequences’.”
The implications of Rasnick’s statement are enormous.
First of all, forget about the idea that SARS-Cov-2 has one genetic sequence.
And these multiple sequences aren’t assembled by looking through a magic microscope. They’re put together by computer programs which have pre-set algorithms.
In other words, the sequences are built by ASSUMPTIONS (not evidence) embedded in the algorithms.
ANY vaccine developed for SARS-Cov-2 (even if you believe in the theory of how vaccines are supposed to work) would face the task of producing immunity to an ever-mutating virus—not just one mutated strain, but endless numbers of mutations.
You would have an analog to seasonal flu, in which researchers make a guess about what the new version of the virus will look like every year and develop a new vaccine for that guess.
How well is this working out? Public health agencies report that, each and every year, there are a BILLION cases of seasonal flu, worldwide.
Going still deeper, if the genetic sequences of the ever-mutating viruses are not discovered, but concocted via computer programs, how likely is it that a vaccine utilizing that “data” would work?
And at the bottom of the whole pile of guesswork, is, of course, the realization that, if these genetic sequences are concocted—where is the ACTUAL isolated virus? WHERE IS THE PROOF THAT IT EXISTS?
Where is it, when, as I’ve been reporting for months now, researchers twist and torture the meaning of “isolated,” so that it indicates “the virus is somewhere in a soup in a dish in a lab”—definitely UN-isolated.
Such is the “science” of modern virology.
But don’t worry, be happy, the test “for the coronavirus” must be accurate, the case and death numbers must be accurate, and the consequent lockdowns which are destroying national economies and hundreds of millions of lives are necessary…right?
Sure. Why not? Let’s say it’s all, all right. Everybody can go back to sleep and let tyrants demolish Earth civilization.
OR, you can REBEL against the Police State built on a house-of-cards hoax called “science.”
As opposed to “the virus,” liberty and freedom are quite real. People can feel them in their bones, in their minds and souls. Even and especially if they are slaves, they can feel them.
Speaking of whether a virus actually exists, here is an article I’ve reposted several times:
DOES HIV EXIST? AN EXPLOSIVE INTERVIEW
Before we get to Christine Johnson’s interview, a bit of background.
My first book, AIDS INC., was published in 1988. The research I engaged in then formed a foundation for my recent work in exposing the vast fraud called COVID-19.
In 1987-88, my main question eventually became: does HIV cause AIDS? For months, I had blithely assumed the obvious answer was yes. This created havoc in my investigation, because I was facing contradictions I couldn’t solve.
For example, in parts of Africa, people who were chronically ill and dying obviously needed no push from a new virus. All their “AIDS” conditions and symptoms could be explained by their environment: contaminated water supplies; sewage pumped directly into the drinking water; protein-calorie malnutrition; hunger, starvation; medical treatment with immunosuppressive vaccines and drugs; toxic pesticides; fertile farm land stolen by corporations and governments; wars; extreme poverty. The virus cover story actually obscured all these ongoing crimes.
Finally, in the summer of 1987, I found several researchers who were rejecting the notion that HIV caused AIDS. Their reports were persuasive.
I’m shortcutting a great deal of my 1987-8 investigation here, but once HIV was out of the picture for me, many pieces fell into place. I discovered that, in EVERY group supposedly at “high-risk” for AIDS, their conditions and symptoms could be entirely explained by factors that had nothing to do with a new virus.
AIDS was not one condition. It was an umbrella label, used to re-package a number of immunosuppressive conditions and create the illusion of a new and unique and single “pandemic.”
Several years after the publication of AIDS INC., I became aware of a quite different emerging debate going on under the surface of research: DOES HIV EXIST?
Was the purported virus ever truly discovered?
And THAT question led to: what is the correct procedure for discovering a new virus?
The following 1997 interview, conducted by brilliant freelance journalist, Christine Johnson, delves into these questions:
How should researchers prove that a particular virus exists? How should they isolate it? What are the correct steps?
These questions, and their answers, reside at the heart of most disease research—and yet, overwhelmingly, doctors never explore them or even consider them.
Johnson interviews Dr. Eleni Papadopulos, “a biophysicist and leader of a group of HIV/AIDS scientists from Perth in Western Australia. Over the past decade and more she and her colleagues have published many scientific papers questioning the HIV/AIDS hypothesis…”
Here I’m publishing and highlighting excerpts from the interview  . Technical issues are discussed. Grasping them is not the easiest exercise you’ve ever done, but I believe the serious reader can comprehend the vital essentials.
CJ: Does HIV cause AIDS?
EP: There is no proof that HIV causes AIDS.
CJ: Why not?
EP: For many reasons, but most importantly, because there is no proof that HIV exists.
… CJ: Didn’t Luc Montagnier and Robert Gallo [purportedly the co-discoverers of HIV] isolate HIV back in the early eighties?
EP: No. In the papers published in Science by those two research groups, there is no proof of the isolation of a retrovirus from AIDS patients. [HIV is said to be a retrovirus.]
CJ: They say they did isolate a virus.
EP: Our interpretation of the data differs. To prove the existence of a virus you need to do three things. First, culture cells and find a particle you think might be a virus. Obviously, at the very least, that particle should look like a virus. Second, you have to devise a method to get that particle on its own so you can take it to pieces and analyze precisely what makes it up. Then you need to prove the particle can make faithful copies of itself. In other words, that it can replicate.
CJ: Can’t you just look down a microscope and say there’s a virus in the cultures?
EP: No, you can’t. Not all particles that look like viruses are viruses.
… CJ: My understanding is that high-speed centrifugation is used to produce samples consisting exclusively of objects having the same density, a so-called “density-purified sample.” Electron microscopy is used to see if these density-purified samples consist of objects which all have the same appearance — in which case the sample is an isolate — and if this appearance matches that of a retrovirus, in terms of size, shape, and so forth. If all this is true, then you are three steps into the procedure for obtaining a retroviral isolate. (1) You have an isolate, and the isolate consists of objects with the same (2) density and (3) appearance of a retrovirus. Then you have to examine this isolate further, to see if the objects in it contain reverse transcriptase [an enzyme] and will replicate when placed in new cultures. Only then can you rightfully declare that you have obtained a retroviral isolate.
EP: Exactly. It was discovered that retroviral particles have a physical property which enables them to be separated from other material in cell cultures. That property is their buoyancy, or density, and this was utilized to purify the particles by a process called density gradient centrifugation.
The technology is complicated, but the concept is extremely simple. You prepare a test tube containing a solution of sucrose, ordinary table sugar, made so the solution is light at the top but gradually becomes heavier, or more dense, towards the bottom. Meanwhile, you grow whatever cells you think may contain your retrovirus. If you’re right, retroviral particles will be released from the cells and pass into the culture fluids. When you think everything is ready, you decant a specimen of culture fluids and gently place a drop on top of the sugar solution. Then you spin the test tube at extremely high speeds. This generates tremendous forces, and particles present in that drop of fluid are forced through the sugar solution until they reach a point where their buoyancy prevents them from penetrating any further. In other words, they drift down the density gradient until they reach a spot where their own density is the same as that region of the sugar solution. When they get there they stop, all together. To use virological jargon, that’s where they band. Retroviruses band at a characteristic point. In sucrose solutions they band at a point where the density is 1.16 gm/ml.
That band can then be selectively extracted and photographed with an electron microscope. The picture is called an electron micrograph, or EM. The electron microscope enables particles the size of retroviruses to be seen, and to be characterized by their appearance.
CJ: So, examination with the electron microscope tells you what fish you’ve caught?
EP: Not only that. It’s the only way to know if you’ve caught a fish. Or anything at all.
CJ: Did Montagnier and Gallo do this?
EP: This is one of the many problems. Montagnier and Gallo did use density gradient banding, but for some unknown reason they did not publish any Ems [photos] of the material at 1.16 gm/ml…this is quite puzzling because in 1973 the Pasteur Institute hosted a meeting attended by scientists, some of whom are now amongst the leading HIV experts. At that meeting the method of retroviral isolation was thoroughly discussed, and photographing the 1.16 band of the density gradient was considered absolutely essential.
CJ: But Montagnier and Gallo did publish photographs of virus particles.
EP: No. Montagnier and Gallo published electron micrographs of culture fluids that had not been centrifuged, or even separated from the culture cells, for that matter. These EMs contained, in addition to many other things, including the culture cells and other things that clearly are not retroviruses, a few particles which Montagnier and Gallo claimed are retroviruses, and which all belonged to the same retroviral species, now called HIV. But photographs of unpurified particles don’t prove that those particles are viruses. The existence of HIV was not established by Montagnier and Gallo — or anyone since — using the method presented at the 1973 meeting.
CJ: And what was that method?
EP: All the steps I have just told you. The only scientific method that exists. Culture cells, find a particle, isolate the particle, take it to pieces, find out what’s inside, and then prove those particles are able to make more of the same with the same constituents when they’re added to a culture of uninfected cells.
CJ: So before AIDS came along there was a well-tried method for proving the existence of a retrovirus, but Montagnier and Gallo did not follow this method?
EP: They used some of the techniques, but they did not undertake every step including proving what particles, if any, are in the 1.16 gm/ml band of the density gradient, the density that defines retroviral particles.
CJ: But what about their pictures?
EP: Montagnier’s and Gallo’s electron micrographs…are of entire cell cultures, or of unpurified fluids from cultures…”
—end of interview excerpt—
If you grasp the essentials of this discussion, you’ll see there is every reason to doubt the existence of HIV, because the methods for proving its existence were not followed.
And so…as I’ve reported these past few months, there is every reason to doubt and reject the existence of the COVID virus, since correct large-scale electron microscope studies have never been done.
I kept the Christine Johnson interview, and other similar information, in mind when, for example, I explored the dud epidemics called SARS and 2009 Swine Flu.
How many viruses have been named as causes of disease, when in fact those viruses have never been isolated or proved to exist?
Of course, conventional-consensus researchers and doctors will scoff at any attempt to raise these issues. For them, “the science is settled.” Meaning: they don’t want to think. They don’t want to stir the waters.
A few years ago, chemist David Rasnick sent a request to the CDC, asking for evidence demonstrating that the Ebola virus had ever been isolated from a human. The answers he received did not begin to approach a level of certainty.
After 30 years working as a reporter in the area of deep medical-research fraud, I’ve seen that false science occurs in levels.
The deeper you go, the stranger it gets. To put it another way: the deeper you go, the worse it gets.
 personal communication
(To read about Jon’s mega-collection, The Matrix Revealed, click here.)
The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.