In the course of an investigation, a clue can turn up that changes everything. It exposes massive falsehoods and fraud.
But the meaning of the clue doesn’t always tap the investigator on the shoulder and reveal its full implications. The force of the rational insight is on a delay mechanism, as it were.
When I was writing my first book, AIDS INC., in the late 1980s, I was surrounded by much confusion. A bewildering number of facts and opinions and lies were being fed to me by various sources. I was taping notes to my walls and trying to sort out the mess of spaghetti.
One day, while I was researching the AIDS antibody test, I spoke to an official at the FDA. He mentioned that, if a vaccine were developed for HIV, anyone who received it would be given a special letter from the government. The letter would declare that if this person ever tested positive for HIV, the result should be ignored, because the antibodies that made the test turn positive were resulting from the protective vaccine, not lethal HIV in the body.
After I hung up the phone, I tried to think through what I had just heard. Something strange was going on. What was it?
About a week later, it hit me. The brain fog was gone.
The official government position implied: if an HIV vaccine were ever developed, it would stimulate antibodies to HIV in the body and thus confer protection against AIDS. But…
If an unvaccinated person, taking an HIV test, registered positive, that result would signal the presence of antibodies to HIV in the body—and THAT would mean the person had AIDS or was on the road to developing it.
However, in either case, THE ANTIBODIES WERE THE SAME.
If they were stimulated and acquired through a vaccine, that was a good sign. It meant immunity.
But if these same antibodies were acquired naturally, as a response to making contact with HIV, that was a bad sign. It meant AIDS, now, or just up the road.
Vaccine antibodies GOOD.
Natural antibodies BAD.
THE SAME ANTIBODIES.
Unintentionally implicit in the FDA spokesman’s statements was the logical walkway called reductio ad absurdum; a reduction to absurdity. In other words, if you took the FDA man’s claim about the letter a person vaccinated against HIV would carry with him—and if you thought it through and saw all the implications, you would see the whole proposal was absurd to the highest degree.
A vaccine would produce an effect, X, which would confer immunity. The body, producing the same effect, X, would signal impending disease and even death.
Medical solution GOOD.
Body’s natural solution BAD.
Time and time again in my investigations, I’ve found reductio ad absurdum to be a very good friend and ally. Aristotle originally formulated the strategy, and it has stood the time of time quite nicely.
The overall pattern is rather simple: take an assertion; understand what it claims; lay out the chain of implications that follow from the assertion; show that this chain leads to an impossible or absurd consequence. THEREFORE, reject the assertion.
It’s like following a faulty set of directions. You drive through various streets and shift from one highway to another, all in the process of finding your way home from a distant location. But the directions finally lead you to a series of barriers at the desolate end of a highway, beyond which there is no road, only a pile of construction materials and a dank dark river you’ve never seen before.
It’s not home. It’s not useful. It makes no sense. It’s reductio ad absurdum.
The idea that a HIV vaccine would confer immunity, while a person’s own body—producing the same antibodies—wouldn’t confer immunity, is preposterous.
In the years since AIDS INC. was published, I’ve written about the sea-change that has occurred in disease diagnosis and vaccine “protection.” These days, a person receiving an antibody test for ANY given disease is told he is “positive” for the disease if antibodies show up on the test. But if he receives a vaccine that produces the same antibodies, he’s told he’s immune.
It makes zero sense.
Here is a final clue. A positive antibody test is no reason to tell a person he is sick or is going to get sick. A positive test most often indicates the person’s immune system has swung into gear and neutralized the germ in question. BUT if the medical establishment decides, arbitrarily, to interpret every positive test as a sign of illness, then many, many more people can be diagnosed with diseases. And then…
They can be treated with drugs.
And then, pharmaceutical cash registers ring like crazy with profits. Read More At: JonRappoport.wordpress.com
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Jon Rappoport
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.
As a freelance reporter, a main thrust of my research over the past 35 years has been medical fraud. Deep fraud. Fraud that takes place in research labs, where “new diseases” are discovered.
I wrote a number of articles about the so-called SARS outbreak of 2003. Health agencies and governments built up a ton of hysteria and sold it to the global public.
A few basic “facts”: Severe acute respiratory syndrome (SARS) includes the following symptoms—cough, fever, fatigue, sore throat. It originated in South China. It is caused by the SARS coronavirus. SARS is unique. It is a newly discovered condition. The coronavirus is newly discovered.
I saw holes in this presentation. For example, the SARS symptoms are indistinguishable from ordinary traditional flu or other non-specific illness that has been known about for centuries.
I kept going.
The SARS coronavirus was purportedly discovered by World Health Organization researchers working in ten labs linked by a private closed-circuit communication system. No outside researchers were given access.
The WHO researchers very quickly found the unique and never-before-seen coronavirus.
No statistics were released that demonstrated how many diagnosed SARS patients had the coronavirus virus in their bodies and how many didn’t.
But months later, a WHO microbiologist in Canada, Frank Plummer, wandered off the reservation and spoke with reporters. What he said, in a series of statements, was shocking:
Plummer basically admitted that almost all of the newest blood samples from SARS patients coming into his lab showed no trace of the SARS coronavirus.
Here is where logic enters the scene. When I reported what Frank Plummer said, I concluded that something was very, very wrong, because…how could people be diagnosed with SARS when they didn’t have the SARS virus in their bodies?
However, even in certain independent media outlets, that conclusion didn’t catch on. People were unable to realize:
If a patient is diagnosed with a disease, and that disease is supposed to be caused by a particular virus, but that patient doesn’t have the virus in his body, he can’t have the disease.
It’s as if you read, “Linguistics researchers at MIT just finished studying the characteristics of 120,000 sentences that contain exactly five words. Their findings are based on sentences that contain four words.”
Red flags, alarm bells, stop signs.
Basic logic has been violated.
But it turns out that a certain percentage of the population doesn’t recognize contradictions. They just pass over them, as if they aren’t there.
“Let’s see. Almost all the newest SARS patients don’t have the SARS virus. Okay. I guess that’s unusual.”
Not unusual. Impossible, by definition.
This is how education works in these times. See a blatant contradiction? Move on. Doesn’t matter. Contradictions are…a matter of opinion. Some people see blue, other people see green.
If you were shepherding society into a new era where control from above would be much tighter, you’d want to decide how the population should think about information—and if you could disable their capacity to the point where blatant contradictions passed unnoticed, you would count that as a victory.
On the other hand, if you were a parent who was prepared to pay a stunning sum of money for your child to attend college, and you knew he would emerge, after four years, unable to tell the difference between “blue” and “not blue,” you might be disturbed.
Consider this: In the wake of microbiologist Frank Plummer’s astonishing remarks to the press in 2003, not one major media news outlet in the world followed up and launched a probing investigation of a SARS scandal. It didn’t happen. It hasn’t happened since.
“A newly discovered disease” with the same symptoms as ordinary seasonal flu is said to be unique, because every person who has it also has a never-before-seen virus EXCEPT FOR THE FACT THAT EVERY PERSON DOESN’T HAVE THE VIRUS.
Memo to college and medical school students: write a thousand words on the logical implications of the above paragraph.
If you can’t, turn around immediately and go back to high school. Stage protests until the school offers a mandatory course in logic taught by a competent instructor.
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.
News outlets are reporting a new Ebola outbreak in Africa. Here is a quick summary of the basic mainstream story—
The Huffington Post cites a World Health Organization (WHO) statement: four people are believed to have died from Ebola in the Congo.
There are 37 more “suspected cases.”
Discussions are underway about using an “experimental vaccine” in the Congo.
WHO has declared the Ebola outbreak an epidemic.
There is an effort to find 400 people believed to have come into contact with the “suspected cases.” Residents in the affected area of the Congo, the remote Bas-Uele province, are fleeing in fear.
That’s it so far.
I’ve been around the block on the Ebola story a dozen times. Here are the issues the press isn’t reporting—
There is one predictable outcome: at Congo clinics and hospitals, frightened people who arrive with what are labeled “early signs” of Ebola will be labeled as probable cases. What are those symptoms? Fever, chill, sore throat, cough, headache, joint pain. Sound familiar? Normally, this would just be called the flu.
Here’s another point you won’t see discussed on the mainstream news: the reliability of tests used to diagnose Ebola.
Two of those major tests—antibody and PCR—are notoriously unreliable.
Antibody tests will register positive for disease because they ping on factors that have nothing to do with the disease being looked for. And even when the test is accurate, a positive reading merely shows that the patient came in contact with the germ in question. It says nothing about whether he’s ill or is going to become ill.
In fact, before 1985, when the science was turned on its head, antibody-positive status was taken to mean the patient’s immune system had successfully warded off the germ.
The PCR test is a sophisticated way of amplifying tiny, tiny bits of what are assumed to be viral material, so they can be observed. The problem here is this: if only tiny bits of material could be found in the patient’s body in the first place, there is no reason to suppose they’re enough to cause disease. Very, very large amounts of virus are necessary to begin to suspect the patient is ill or is going to become ill.
Bottom line: huge numbers of people on whom these tests are done are going to be falsely diagnosed with Ebola.
Here is what I wrote about the Ebola outbreak of 2014 in Africa. It applies today:
Ebola, covert op in a hypnotized world, August 2, 2014:
You show people a germ and you tell them what it is and what it does, and people salute. They give in. They believe. They actually know nothing. But they believe.
The massive campaign to make people believe the Ebola virus can attack at any moment, after the slightest contact, is quite a success.
People are falling all over themselves to raise the level of hysteria.
This is what is preventing a hard look at Liberia, Sierra Leone, and the Republic Guinea, three African nations where poverty and illness are staples of everyday life for the overwhelming number of people.
The command structure in those areas has a single dictum: don’t solve the human problem.
Don’t clean up the contaminated water supplies, don’t return stolen land to the people so they can grow food and finally achieve nutritional health, don’t solve overcrowding, don’t install basic sanitation, don’t strengthen their immune systems so they can ward off germs, don’t let the people have power—because then they would throw off the local and global corporate juggernauts that are sucking the land of all its resources.
In order not to solve the problems of the people, a cover story is necessary. A cover story that exonerates the power structure.
A cover story like a germ.
It’s all about the germ. The demon. The strange attacker.
Forget everything else. The germ is the single enemy.
Forget the fact, for example, that a recent study of 15 pharmacies and 5 hospital drug dispensaries in Sierra Leone discovered the widespread and unconscionable use of beta-lactam antibiotics.
These drugs are highly toxic. One of their effects? Excessive bleeding.
Which just happens to be the scary “Ebola effect” that’s being trumpeted in the world press.
(J Clin Microbiol, July 2013, 51(7), 2435-2438), and Annals of Internal Medicine Dec. 1986, “Potential for bleeding with the new beta-lactam antibiotics”)
Forget the fact that pesticide companies are notorious for shipping banned toxic pesticides to Africa. One effect of the chemicals? Bleeding.
Forget that. It’s all about the germ and nothing but the germ.
Forget the fact that, for decades, one of the leading causes of death in the Third World has been uncontrolled diarrhea. Electrolytes are drained from the body, and the adult or the baby dies. (Diarrhea is also listed as an “Ebola” symptom.)
Any sane doctor would make it his first order of business to replace electrolytes with simple supplementation—but no, the standard medical line goes this way:
The diarrhea is caused by germs in the intestinal tract, so we must pile on massive amounts of antibiotics to kill the germs.
The drugs kill off all bacteria in the gut, including the necessary and beneficial ones, and the patient can’t absorb what little food he has access to, and he dies.
Along the way, he can also bleed.
But no, all the bleeding comes from Ebola. It’s the germ. Don’t think about anything else.
Forget the fact that adenovirus vaccines, which have been used in Liberia, Guinea, and Liberia (the epicenter of Ebola), have, according to vaccines.gov, the following adverse effects: blood in the urine or stool, and diarrhea.
No, all the bleeding comes from the Ebola germ. Of course. Don’t think about anything else.
Reporter Charles Yates uncovered a scandal in Liberia centering around the Firestone Rubber Plantation—chemical dumping, poisoned water.
And skin disease.
“Rash” is listed as one of the Ebola symptoms.
Liberia Coca Cola bottling plant: foul black liquid seeping into the environment—animals dying.
Chronic malnutrition and starvation—conditions that are endemic in Liberia, Sierra Leone, and Guinea—are the number-one cause of T-cells depletion in the world.
T-cells are a vital component of the immune system. When that system is compromised, any germ coming down the pipeline will cause epidemics and death.
Getting the picture?
But no, blame it all on the germ.
Allow the corporate-government domination to continue.
—end of my 2014 article—
There is more, but I’ll leave it there for the moment.
The mainstream story about Ebola is riddled with hoax.
It’s “blame the virus” for illness and dying that come from other obvious sources. Read More At: JonRappoport.wordpress.com
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Jon Rappoport
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.
Source: NaturalBlaze.com
Heather Callahan
April 26, 2017
But don’t worry…….they don’t bite?
The biggest trend for mad scientists now is the Aedes aegypti mosquitoes – the same mosquitoes that are noted for carrying tropical diseases and for getting genetically engineered under the guise of fighting the Zika. Zika is one of the latest banners of scare porn that the mainstream media has foisted on the public in a seeming attempt to pave the way for biotech companies to operate unhindered.
Thousands of mosquitoes infected with the Wolbachia bacteria were released in an area of the Florida Keys this week, in hopes of a new approach to control the disease-carrying female Aedes aegypti mosquito, which transmits Zika virus, Dengue fever and Chikungunya.
According to the Florida Keys Mosquito Control District, 20,000 male Aedes aegypti mosquitoes were released on Stock Island Tuesday for a field trial that will last 12 weeks. The mosquitoes, which do not bite, have been manually infected with a naturally occurring bacteria called Wolbachia.
The Wolbachia-infected mosquitoes are to be released twice a week at 20 different spots in the “designated area” for the trial for MosquitoMate. The public was apparently warned that there would be an (ironic) influx of mosquitoes during this time.
CNN adds:
As explained in a presentation by the Florida Keys Mosquito Control District, when these infected male Aedes aegypti mosquitoes mate with female Aedes aegypti mosquitoes, the eggs she produces won’t hatch, thus they can’t reproduce. The result, they hope, will be a reduced or eliminated population of female Aedes aegypti mosquitoes and the viruses they spread, including Zika virus.
Similar to the GE mosquitoes that British company Oxitec are trying to release, the offspring die but in this case it is the mechanism of the bacteria doing it.
MosquitoMate claims that their mosquitoes are non-GMO and apparently they have already been released in Kentucky, California an New York. They work closely with University of Kentucky and say, “We rely on a natural approach rather than GMO to reduce the mosquito population in your backyard. We utilize a naturally-occurring bacterium called Wolbachia, which is present in insect cells, to infect our male mosquitoes.” Sounds pretty natural right? Injecting an unnaturally occurring bacterium into the mosquitoes before release…
Then the report goes on to say more scary things about Zika and pregnant women who could have babies born with microcephaly – a link that is questionable.
Andrea Leal, executive director for the Florida Keys Mosquito Control District said:
A successful trial with the Wolbachia-infected mosquitoes could mean the availability of a new tool in the fight against the Aedes aegypti mosquito for not only our District, but for Mosquito Control Districts around the country.
Floridians have been rejecting the release of British company Oxitec’s genetically modified mosquitoes for some time. Is this little “experiment” a way to finally release some type of modified pest?
Florida’s elected are still trying to push for Oxitec’s field trials on the public. It would include the release of thousands of GE mosquitoes. A similar push is happening in Houston, TXby – you guessed it – Oxitec! They just keep buzzing to other locations since they already received FDA approval.
Oxitec also conducted field trials in Brazil, Panama and the Cayman Islands. The company boasts that it has reduced the Aedes mosquito populations by up to 90 percent each time. One has to wonder what the ecological impact is for other animals, like bats and frogs, who may actually be losing most of their food supply. Another thing to consider is that the newly mutated offspring can actually survive maturity if they are antidoted with the antibiotic tetracycline.
One wonders what will happen in a future of competing biotech companies – will their experiments overlap or will the government simply dole out territories with which they can test their patented creatures?
So – don’t you love how the media just tells you what you get to accept and then juxtapose the scary reason why an unacceptable action has to take place right now?
Groundbreaking research indicates that nearly everything we once believed about the purportedly deadly properties of flu virus may be based on institutionalized superstition and myth.
Germ theory is an immensely powerful force on this planet, affecting everyday interactions from a handshake, all the way up the ladder to national vaccination agendas and global eradication campaigns. But what if fundamental research on what exactly these ‘pathogens’ are, how they infect us, has not yet even been performed? What if much of what is assumed and believed about the danger of microbes, particularly viruses, has completely been undermined in light of radical new discoveries in microbiology?
Some of our readers already know that in my previous writings I discuss why the “germs as our enemies” concept has been decimated by the relatively recent discovery of the microbiome. For background, feel free to read “How The Microbiome Destroyed the Ego, Vaccine Policy, and Patriarchy.”
In today’s article, I will take a less philosophical approach, and focus on influenza as a more concrete example of the Copernican-level paradigm shift in biomedicine and life sciences we are all presently fully immersed within, even if many in the establishment have yet to fully acknowledge it.
Deadly Flu Viruses: Vaccinate or Die?
The way health policy makers talk about it today, flu virus is a deadly force, against which all citizens, of all ages 6 months or older, need to take an annual influenza vaccine to protect themselves against, lest they face deadly consequences. Worse, those who hold religious or philosophical objections, or who otherwise conscientiously object to vaccinating, are being characterized as doing harm to others by denying them herd immunity (a concept that has been completely debunked by a careful study of the evidence, or lack thereof). For instance, in the interview below Bill Gates tells Sanjay Gupta that he thinks non-vaccinators “kill children”:
But what if I told you that there isn’t even such a thing as “flu virus,” in the sense of a monolithic, disease vector existing outside of us, conceived as it is as the relationship of predator to prey?
First, consider that the highly authorative Cochrane collaboration acknowledges there are many different flu viruses that are not, in fact, influenza A — against which flu vaccines are targeted — but which nonetheless can contribute to symptoms identical to those attributed to influenza A:
“Over 200 viruses cause influenza and influenza-like illness which produce the same symptoms (fever, headache, aches and pains, cough and runny noses). Without laboratory tests, doctors cannot tell the two illnesses apart. Both last for days and rarely lead to death or serious illness. At best, vaccines might be effective against only Influenza A and B, which represent about 10% of all circulating viruses.” (Source: Cochrane Summaries).” [emphasis added]
This makes for a picture of complexity that powerfully undermines health policies that presuppose vaccination equates to bona fide immunity, and by implication, necessitates the herd collectively participate in the ritual of mass vaccination campaigns as a matter of social responsibility and necessity.
Even the use of the word “immunization” to describe vaccination is highly misleading. The moment the word is used, it already presupposes efficacy, and makes it appear as if non-vaccinators are anti-immunity, instead of what they actually are: pro-immunity (via clean air, food, water, and sunlight), but unwilling to subject themselves or their healthy children to “unavoidably unsafe” medical procedures with only theoretical benefits.
Why Flu Virus Doesn’t Exist (The Way We Were Told)
But the topic gets even more interesting when we consider the findings of a 2015 study entitled “Conserved and host-specific features of influenza vision architecture.” This was the first study ever to plumb the molecular depths of what influenza virus is actually composed of. Amazingly, given the long history of vaccine use and promotion, the full characterization of what proteins it contains, and where they are derived from, was never previously performed. How we invest billions of dollars annually into flu vaccines, and have created a global campaign to countermand a viral enemy, whose basic building blocks we don’t even know, is hard to understand. But it is true nonetheless.
The study abstract opens with this highly provocative line:
“Viruses use virions to spread between hosts, and virion composition is therefore the primary determinant of viral transmissibility and immunogenicity.” [emphasis added]
Virion are also known as “viral particles,” and they are the means by which viral nucleic acids are able to move and ‘infect’ living organisms. Without the viral particle (taxi) to carry around the virus DNA (passenger), it would be harmless; in fact, viruses are often described as existing somewhere between living and inanimate objects for this reason: they do not produce their own energy, nor are transmissable without a living host. And so, in this first line, the authors are making it clear that virion composition is also the primary determinant in how or whether a virus is infectious (transmits) and what affects it will have in the immune system of the infected host.
Influenza viral particles.
This distinction is important because we often think of viruses as simply pathogenic strings of DNA or RNA. The irony, of course, is that the very things we attribute so much lethality to — viral nucleic acids — are not even alive, and can not infect an organism without all the other components (proteins, lipids, extra-viral nucleic acids) which are, technically, not viral in origin, participating in the process. And so, if the components that are non-viral are essential for the virus to cause harm, how can we continue to maintain that we up against a monolithic disease entity “out there” who “infects” us, a passive victim? It’s fundamentally non-sensical, given these findings. It also clearly undermines the incessant, fear-based rhetoric those beholden to the pro-vaccine use to coerce the masses into undergoing the largely faith-based rite of vaccination.
Let’s dive deeper into the study’s findings…
The next line of the abstract addresses the fact we opened this article with: namely, that there is great complexity involved at the level of the profound variability in virion composition:
“However, the virions of many viruses are complex and pleomorphic, making them difficult to analyze in detail”
But this problem of the great variability in the virion composition of influenza is exactly why the study was conducted. They explain:
“Here we address this by identifying and quantifying viral proteins with mass spectrometry, producing a complete and quantifiable model of the hundreds of viral and host-encoded proteins that make up the pleomorphic virions of influenza virus. We show that a conserved influenza virion architecture, which includes substantial quantities of host proteins as well as the viral protein NSI, is elaborated with abundant host-dependent features. As a result, influenza virions produced by mammalian and avian hosts have distinct protein compositions.”
In other words, they found that the flu virus is as much comprised of biological material from the host the virus ‘infects,’ as the viral genetic material of the virus per se.
How then, do we differentiate influenza virus as fully “other”? Given that it would not exist without “self” proteins, or those of other host animals like birds (avian) or insects, this would be impossible to do with any intellectual honesty intact.
There’s also the significant problem presented by flu vaccine production. Presently, human flu vaccine antigen is produced via insects and chicken eggs. This means that the virus particles extracted from these hosts would contain foreign proteins, and would therefore produce different and/or unpredictable immunological responses in humans than would be expected from human influenza viral particles. One possibility is that the dozens of foreign proteins found within avian influenza could theoretically produce antigens in humans that cross-react with self-structures resulting in autoimmunity. Safety testing, presently, does not test for these cross reactions. Clearly, this discovery opens up a pandora’s box of potential problems that have never sufficiently been analyzed, since it was never understood until now that “influenza” is so thoroughly dependent upon a host for its transmissability and immunogenecity.
Are Flu Viruses Really “Hijacked” Exosomes?
Lastly, the study identified something even more amazing:
“Finally, we note that influenza virions share an underlying protein composition with exosomes, suggesting that influenza virions form by subverting micro vesicle” production.”
What these researchers are talking about is the discovery that virion particles share stunning similarities to naturally occurring virus-like particles produced by all living cells called exosomes. Exosomes, like many viruses (i.e. enveloped viruses) are enclosed in a membrane, and are within the 50-100 nanometer size range that viruses are (20-400 nm). They also contain biologically active molecules, such as proteins and lipids, as well as information-containing ones like RNAs — exactly, or very similar, to the types of contents you find in viral particles.
Watch this basic video on exosomes to get a primer:
In light of this post-Germ Theory perspective, viruses could be described as pieces of information in search of chromosomes; not inherently “bad,” but, in fact, essential for mediating the genotype/phenotype relationship within organisms, who must adapt to ever-shifting environmental conditions in real-time in order to survive; something the glacial pace of genetic changes within the primary nucleotide sequences of our DNA cannot do (for instance, it may take ~ 100,000 years for a protein-coding gene sequence to change versus seconds for a protein-coding gene’s expression to be altered via modulation via viral or exosomal RNAs).
This does not mean they are “all good,” either. Sometimes, given many conditions outside their control, their messages could present challenges or misinformation to the cells to which they are exposed, which could result in a “disease symptom.” But with the caveat that these disease symptoms are often if not invariably attempts by the body to self-regulate and ultimately improve and heal itself.
In other words, the virion composition of viruses appears to be the byproduct of the cell’s normal exosome (also known as microvessicle) production machinery and trafficking, albeit being influenced by influenza DNA. And like exosomes, viruses may be a means of extracellular communication between cells, instead of simply a pathological disease entity. This could explain why an accumulating body of research on the role of the virome in human health indicates that so-called infectious agents, including viruses like measles, confer significant health benefits. [see: the Health Benefits of Measles and The Healing Power of Germs?].
Other researchers have come to similar discoveries about the relationship between exosomes and viruses, sometimes describing viral hijacking of exosome pathways as a “Trojan horse” hypothesis. HIV may provide such an example.
Concluding Remarks
The remarkably recent discovery of the host-dependent nature of the influenza virus’ virion composition is really just the tip of an intellectual iceberg that has yet to fully emerge into the light of day, but is already “sinking” ships; paradigm ships, if you will.
One such paradigm is that germs are enemy combatants, and that viruses serve no fundamental role in our health, and should be eradicated from the earth with drugs and vaccines, if possible.
This belief, however, is untenable. With the discovery of the indispensable role of the microbiome, and the subpopulation of viruses within it — the virome — we have entered into an entirely new, ecologically-based view of the body and its environs that are fundamentally inseparable. Ironically, the only thing that influenza may be capable of killing is germ theory itself.
For an in-depth exploration of this, watch the lecture below on the virome. I promise, if you do so, you will no longer be able to uphold germ theory as a monolithic truth any longer. You may even start to understand how we might consider some viruses “our friends,” and why we may need viruses far more than they need us.
In many previous articles, I’ve established there is no convincing evidence the Zika virus causes the birth defect called microcephaly. (Zika archive here)
Basically, Brazilian researchers, in the heart of the purported “microcephaly epidemic,” decided to stop their own investigation and simply assert Zika was the culprit. At that point, they claimed that, out of 854 cases of microcephaly, only 97 showed “some relationship” to Zika.
You need to understand that these figures actually show evidence AGAINST Zika. When researchers are trying to find the cause of a condition, they should be able to establish, as a first step, that the cause is present in all cases (or certainly an overwhelming percentage).
This never happened. The correlation between the presence of Zika and microcephaly was very, very weak.
As a second vital step, researchers should be able to show that the causative virus is, in every case, present in large amounts in the body. Otherwise, there is not enough of it to create harm. MERE PRESENCE OF THE VIRUS IS NOT ENOUGH. With Zika, proof it was present in microcephaly-babies in large amounts has never been shown.
But researchers pressed on. A touted study in the New England Journal of Medicine claimed Zika infected brain cells in the lab. IRRELEVANT. Cells in labs are not human beings. The study also stated that Zika infected baby mice. IRRELEVANT. Mice are not humans. And these mice in the lab had been specially altered or bred to be “vulnerable to Zika.” USELESS AND IRRELEVANT.
All this fraud set the stage for the Zika DNA vaccine. Yes, it is under development. It is, in fact, an example of the next generation of vaccines. And this is why you should watch out.
Here is an excerpt from a US National Institutes of Health press release (8/3/16) (here, here, and, the booster to the DNA vaccine here):
“The National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health [NIH], has launched a clinical trial of a vaccine candidate intended to prevent Zika virus infection.”
“Scientists at NIAID’s Vaccine Research Center (VRC) developed the investigational vaccine — called the NIAID Zika virus investigational DNA vaccine — earlier this year.”
“The investigational Zika vaccine includes a small, circular piece of DNA — called a plasmid — that scientists engineered to contain genes that code for proteins of the Zika virus. When the vaccine is injected into the arm muscle, cells [in the person’s body] read the genes and make Zika virus proteins, which self-assemble into virus-like particles. The body mounts an immune response to these particles, including neutralizing antibodies and T cells. DNA vaccines do not contain infectious material — so they cannot cause a vaccinated individual to become infected with Zika — and have been shown to be safe in previous clinical trials for other diseases.”
SYNTHESIZED GENES ARE INJECTED INTO THE BODY.
That’s why it’s called a DNA vaccine.
Beginning to wonder what this is all about?
It’s about PERMANENTLY ALTERING YOUR DNA.
It’s about altering the DNA of every person on the planet who is vaccinated.
New York Times, 3/9/15, “Protection Without a Vaccine.” The article describes the frontier of research. Here are key quotes that illustrate the use of synthetic genes to “protect against disease,” while changing the genetic makeup of humans. This is not science fiction:
“By delivering synthetic genes into the muscles of the [experimental] monkeys, the scientists are essentially re-engineering the animals to resist disease.”
“’The sky’s the limit,’ said Michael Farzan, an immunologist at Scripps and lead author of the new study.”
“The first human trial based on this strategy — called immunoprophylaxis by gene transfer, or I.G.T. — is underway, and several new ones are planned.” [That was nearly two years ago.]
“I.G.T. is altogether different from traditional vaccination. It is instead a form of gene therapy. Scientists isolate the genes that produce powerful antibodies against certain diseases and then synthesize artificial versions. The genes are placed into viruses and injected into human tissue, usually muscle.”
Here is the punchline: “The viruses invade human cells with their DNA payloads, and the synthetic gene is incorporated into the recipient’s own DNA. If all goes well, the new genes instruct the cells to begin manufacturing powerful antibodies.”
Read that again: “the synthetic gene is incorporated into the recipient’s own DNA.”
Alteration of the human genetic makeup.
Not just a “visit.” Permanent residence. And once a person’s DNA is changed, doesn’t it follow that he/she will pass on that change to the next generation of children, and so on, down the line?
The Times article taps Nobel laureate Dr. David Baltimore for an opinion:
“Still, Dr. Baltimore says that he envisions that some people might be leery of a vaccination strategy that means altering their own DNA, even if it prevents a potentially fatal disease.”
By now you should be seeing the larger picture. A virus (Zika)…
Never proved to cause anything…
Becomes the occasion for developing and injecting a vaccine…
That is actually a group of synthetic genes…
Which will alter your DNA.
And that program implies the possibility of a far wider operation:
Covertly, any genes can be injected in the body and called vaccination. Untold numbers of experiments to alter human DNA can be run. Experiments to create more obedient and passive people, more intelligent and talented people, soldiers who have much higher pain thresholds and who will accept orders without thought or question…
And if you think that is science fiction, read these words from biophysicist Gregory Stock, former director of the program in Medicine, Technology, and Society at the UCLA School of Medicine, to get a glimpse of what “the best and the brightest” are considering:
“Even if half the world’s species were lost [during genetic experiments], enormous diversity would still remain. When those in the distant future look back on this period of history, they will likely see it not as the era when the natural environment was impoverished, but as the age when a plethora of new forms—some biological, some technological, some a combination of the two—burst onto the scene. We best serve ourselves, as well as future generations, by focusing on the short-term consequences of our actions rather than our vague notions about the needs of the distant future.”
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.
Imagine men in bleach white bio suits with medical masks show up at your door. You are suspected of carrying a communicable disease. You will now be arrested and held without due process, indefinitely.
The government could do this any day.
They have the “authority”. They have the personnel. They have the funding. Now all they need is the excuse.
The Authority
The federal government claims the right to quarantine anyone who they suspect has or has come into contact with a communicable disease.
On January 19th of this year, a regulation was passed by the Centers for Disease Control (CDC) and Department of Health and Human Services (HHS).
The regulation is meant to allow the HHS and other departments of the federal government to stop the spread of contagious diseases, like Ebola or bird flu. But the regulation is obscure enough to be a serious threat to liberty.
Because the government does not consider quarantine an arrest, those being detained are not afforded the same rights and due process that criminals are supposed to get through the U.S. Justice system.
Apprehension and detention of persons with quarantinable communicable diseases.
(a) The Director may authorize the apprehension, medical examination, quarantine, isolation, or conditional release of any individual for the purpose of preventing the introduction, transmission, and spread of quarantinable communicable diseases, as specified by Executive Order, based upon a finding that:
(1) The individual is reasonably believed to be infected with a quarantinable communicable disease in a qualifying stage and is moving or about to move from a State into another State; or
(2) The individual is reasonably believed to be infected with a quarantinable communicable disease in a qualifying stage and constitutes a probable source of infection to other individuals who may be moving from a State into another State.
That pretty much covers everyone, in a sly little trick to make this regulation somehow apply to interstate commerce. Anyone living in America risks coming into contact with someone who might physically move into another state.
And a person must simply be “reasonably believed” to be infected or have come into contact with an infection, which again is a very low standard that could easily apply to almost anyone who has recently gone out in public. Even when they define “reasonably believed,” the CDC and HHS use obscure language so that the definition could basically fit anyone.
Reasonably believed to be infected, as applied to an individual, means specific articulable facts upon which a public health officer could reasonably draw the inference that an individual has been exposed, either directly or indirectly, to the infectious agent that causes a quarantinable communicable disease, as through contact with an infected person or an infected person’s bodily fluids, a contaminated environment, or through an intermediate host or vector, and that as a consequence of the exposure, the individual is or may be harboring in the body the infectious agent of that quarantinable communicable disease.
Indirectly being exposed to a contaminated environment could get you quarantined. That doesn’t sound like a very strict standard, nor does it sound like a well defined parameter for apprehension. Basically anyone could think up a “reasonable” suspicion that someone has been exposed to a disease that would require quarantine.
The regulation says those quarantined will be allowed representation, but what good will this representative do? The government has all the obscure “authority” they need to keep you on lock down.
The regulation also allows the government to conduct screenings “through non-invasive procedures determined appropriate” at airports, bus stations, and other public places, where people may be required to provide contact information.
And there is the obscure limit again: “determined appropriate.” It is a safe bet that the government will determine any action it takes as “appropriate”.
This means people will be compelled to answer the government’s questions and provide information against their will. Since carrying a disease is not guilt of a crime, the CDC and HHS believe that this does not violate the Fifth Amendment protections against being compelled to give testimony that may incriminate you.
As for how this doesn’t violate the Fourth Amendment against unreasonable search and seizure, the regulation sites some legal precedents for how the government can legally violate your rights.
And the same will apply after apprehension where during a forced medical exam, you may also be required to provide further health details about yourself to the authorities.
A thousands strong army of medical police is ready to be activated by the government, and spring into action in case of an epidemic.
SEC. 5210 ESTABLISHING A READY RESERVE CORPS
Section 203 of the Public Health Service Act (42 U.S.C. 204) is amended to read as follows:
SEC. 203 COMMISSIONED CORPS AND READY RESERVE CORPS
‘(a) Establishment-
‘(1) IN GENERAL- There shall be in the Service a commissioned Regular Corps and a Ready Reserve Corps for service in time of national emergency.
‘(2) REQUIREMENT- All commissioned officers shall be citizens of the United States and shall be appointed without regard to the civil-service laws and compensated without regard to the Classification Act of 1923, as amended.
Notice that officers are appointed “without regard to the civil-service laws.” These are laws designed to remove politics as a consideration when hiring in the public sector. They also establish guidelines based on merit, impartial hiring criteria, and safety from arbitrary firing and unwarranted disciplinary action.
Officers are also chosen “without regard to the Classification Act of 1923,” which established merit pay and compensation based on performance.
To be clear, the bill states these laws will be disregarded when appointing this police force. So these officers have been hired based on no known criteria, without any defined qualifications, can be denied for no particular reason, can be fired for any reason whatsoever, paid without regard to merit, and punished or rewarded independently of performance.
That section basically ensures the Ready Reserve Corps can be a politicized group that will follow orders of whoever appoints them.
The Funding
Most of the provisions discussed are already well funded through the Centers for Disease Control, and Department of Health and Human Services. But another source to bolster the government quarantine capabilities is making its way through congress.
The bill, which has passed the House and is now in the Senate, wants the government to be able to deal with “surge capacity” in the event of an epidemic.
It would use certain Homeland Security grants and funds for “enhancing medical preparedness, medical surge capacity, and mass prophylaxis capabilities.”
The Excuse
We’ve heard about some disease every year with the potential to cause mass casualties in the event of an outbreak. It is difficult to tell sometimes how much of the hype is media driven, versus which diseases are of real concern.
But there is actual risk for an eventual epidemic. In China, a particularly deadly strain of bird flu is more prevalent this year than in the past four years.
The Spanish Flu epidemic of 1918 which killed tens of millions of people worldwide, is believed to have started in China in a similar fashion. All it takes is the right mutation of the flu virus to become deadly.
So in a sense, the government should be prepared for such an event, but that doesn’t mean they have to violate rights in order to keep the public safe.
It is important to remember that when protecting the public health, the concern is for the general population and not individuals. That is why regulations like this one open up the possibility that individuals will be severely mistreated, in the name of stopping a contagious outbreak.
If the government does implement the forced quarantine of individuals, whether the excuse is real or fabricated, individuals have cause to fear for their safety under government detainment.
CBS has published the names of sites they claim are fake news. Well, what about CBS itself?
Unless you’ve been living in a cave, you’re aware that a film, Vaxxed, has been showing in theaters across America and overseas—and audiences are stunned by its revelations.
Vaxxed exposes a huge scandal at the CDC, where a long-time researcher, William Thompson, confessed (2014) that he and colleagues committed gross fraud in a study of the MMR vaccine.
Thompson admitted the evidence showed the vaccine led to a higher risk of autism in children—but that finding was intentionally buried, and the vaccine was given a free pass.
Of course, mainstream reporters have been mercilessly attacking Vaxxed, and a segment of the population finds it impossible to believe that the CDC would ever commit this kind of fraud.
So, as a mind-changer, let me take you back to the late summer of 2009, and the Swine Flu epidemic, which was hyped to the sky by the CDC. The Agency was calling for all Americans to take the Swine Flu vaccine. Remember?
The problem was, the CDC was concealing another scandal.
At the time, star CBS investigative reporter, Sharyl Attkisson, was working on a Swine Flu story. She discovered that the CDC had secretly stopped counting cases of the illness—while, of course, continuing to warn Americans about its unchecked spread.
Understand that the CDC’s main job is counting cases and reporting the numbers.
What was the Agency up to?
Here is an excerpt from my 2014 interview with Sharyl Attkisson:
Rappoport: In 2009, you spearheaded coverage of the so-called Swine Flu pandemic. You discovered that, in the summer of 2009, the Centers for Disease Control, ignoring their federal mandate, [secretly] stopped counting Swine Flu cases in America. Yet they continued to stir up fear about the “pandemic,” without having any real measure of its impact. Wasn’t that another investigation of yours that was shut down? Wasn’t there more to find out?
Attkisson: The implications of the story were even worse than that. We discovered through our FOI efforts that before the CDC mysteriously stopped counting Swine Flu cases, they had learned that almost none of the cases they had counted as Swine Flu was, in fact, Swine Flu or any sort of flu at all! The interest in the story from one [CBS] executive was very enthusiastic. He said it was “the most original story” he’d seen on the whole Swine Flu epidemic. But others pushed to stop it [after it was published on the CBS News website] and, in the end, no [CBS television news] broadcast wanted to touch it. We aired numerous stories pumping up the idea of an epidemic, but not the one that would shed original, new light on all the hype. It was fair, accurate, legally approved and a heck of a story. With the CDC keeping the true Swine Flu stats secret, it meant that many in the public took and gave their children an experimental vaccine that may not have been necessary.
—end of interview excerpt—
I’ll add a few details. It was routine for doctors all over America to send blood samples from patients they’d diagnosed with Swine Flu, or the “most likely” Swine Flu patients, to labs for testing. And overwhelmingly, those samples were coming back with the result: not Swine Flu, not any kind of flu.
That was the big secret. That’s what the CDC was hiding. That’s why they stopped reporting Swine Flu case numbers. That’s what Attkisson had discovered. That’s why she was shut down.
But it gets even worse.
Because about three weeks after Attkisson’s findings were published on the CBS News website, the CDC, obviously in a panic, decided to double down. If one lie is exposed, tell an even bigger one. A much bigger one.
Here, from a November 12, 2009, WebMD article is the CDC’s response: “Shockingly, 14 million to 34 million U.S. residents — the CDC’s best guess is 22 million — came down with H1N1 swine flu by Oct. 17 [2009].” (“22 million cases of Swine Flu in US,” by Daniel J. DeNoon).
Are your eyeballs popping? They should be.
In the summer of 2009, the CDC secretly stops counting Swine Flu cases in America, because the overwhelming percentage of lab tests from likely Swine Flu patients shows no sign of Swine Flu or any other kind of flu.
There is no Swine Flu epidemic.
Then, the CDC estimates there are 22 MILLION cases of Swine Flu in the US.
So…the premise that the CDC would never lie about important matters like, oh, a vaccine increasing the risk of autism…you can lay that one to rest.
The CDC will lie about anything it wants to. It will boldly go where no person interested in real science will go.
It will completely ignore its mandate to care about human health, and it will get away with it.
And CBS will conveniently forget how it aided and abetted the CDC, by censoring real news, and instead opted for egregious and titanic fake news.
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.
Source: ActivistPost.com
Catherine Frompovich
February 14, 2017
If the Rand Corporation found strong evidence vaccines cause Guillain-Barre Syndrome (GBS), myalgia, seizures, meningitis, encephalitis and other adverse health problems, and Robert F Kennedy Jr., Esq. is revealing more and more research—almost daily—this time from the Yale School of Medicine and Penn State College of Medicine about an association between vaccines and brain disorders [1], then what’s all the ‘tap dancing’ about? Let’s get to some serious conclusions.
Like tap dancing that makes a lot of noise, so too are vaccine studies peripherally pointing to real vaccine concerns about which the U.S. federal health agencies (HHS, CDC and FDA) and state health departments probably won’t do anything to correct, i.e., eliminate vaccines, as some countries are doing with some vaccines. The ever-increasing—“growing like Topsy”—CDC vaccine schedule has to stop! With almost three hundred new vaccines in production, how many will infants, toddlers and teens be mandated to receive when those vaccines obtain licensure? Furthermore, aren’t vaccines Big Pharma’s annuity products, so what should consumers expect?
All one ever hears is more research has to be done! That seems to be the mantra for all science today.
Personally, I don’t think there ever will be enough research to ‘satisfy’ vaccine inventors, manufacturers, pushers, acolytes and those implementing certain population agendas that vaccines are harmful to human health, especially the developing immune and central nervous systems in infants, toddlers and children.
The research is there!
My book, Vaccination Voodoo, What YOU Don’t Know About Vaccines, cites innumerable studies and peer reviewed scientific articles the U.S. Congress, Big Pharma and CDC/FDA deliberately ignore because, if they took them seriously, it would demand they implement dramatic changes, especially enforcing the Precautionary Principle [3].
According to Robert Kennedy’s latest article,
More than 95,000 children in the database that were analyzed had one of seven neuropsychiatric disorders: anorexia nervosa, anxiety disorder, attention deficit and hyperactivity disorder (ADHD), bipolar disorder, major depression, obsessive-compulsive disorder (OCD) and tic disorder. [1]
Furthermore, others over the years have found similar consequences. For instance, consider what Dr Timothy Craig, Division of Allergy, Asthma and Immunology at Penn State Hershey, had to say:
Antibiotics and vaccines, while protecting us from dangerous and serious diseases, have also weakened our resistance to allergies and asthma. [2] [CJF emphasis added]
That statement, in my opinion, exemplifies the trade-off that’s taking place within the human organism, especially in young children: a seriously weakened or impaired immune system, which leads to chronic diseases earlier in life. This article, “America’s New Normal: Chronically Ill Kids” needs to be taken seriously.
According to the University of Michigan “Michigan Medicine” [4]:
Chronic condition is an “umbrella” term. Children with chronic illnesses may be ill or well at any given time, but they are always living with their condition. Some examples of chronic conditions include (but are not limited to):
Asthma (the most common)
Diabetes
Cerebral palsy
Sickle cell anemia
Cystic fibrosis
Cancer
AIDS
Epilepsy
Spina bifida
Congenital heart problems
I don’t know about you, but I find the chart below published at Focus for Health [5] most revealing:
I got news for you: We never had such statistics regarding chronic diseases in children. There were routine infectious childhood diseases, which I offer help strengthen the immune system—a fine tune for later in life by providing lifelong immunities.
Vaccines effectively are reprogramming and changing the human immune system from its innate capabilities to a pharmacologically-induced “adaptive or acquired” immunity, which demands vaccines and booster shots to maintain some ‘semblance’ of Big Pharma’s definition of “immunity.”
There has been a ‘comfortable’ trade-off of infectious diseases for chronic, lifelong illnesses where patients will be dependent upon Big Pharma meds for the rest of their lives. According to Focus for Health, “Approximately 27% of U.S. children live with chronic health conditions that can affect their daily lives and normal activities.”
Going from 12.8% in 1996 to 26.6% in 2006 statistics for chronic disease must be taken in proper context of correlation and causation, e.g., the number of vaccines for infants and toddlers on the CDC’s vaccine schedule and the growing trend in childhood chronic diseases. According to the CDC’s National Center for Health Statistics, the leading cause of death in children ages one to four years is “congenital malformations, deformations and chromosomal abnormalities.” For children five to fourteen years of age, it’s “cancer.” [7]
Take a look at this comparative vaccine schedule chart 1983 versus 2015 from Peaceful Parent: [6]
Ten vaccines in 1983 to 36-38 in 2015! That’s an almost a 400 percent increase!
I’d say that’s a pretty good return on their propaganda investment that vaccines are ‘safe, effective and life-saving’! Big Pharma was able to hoodwink the U.S. Congress into passing the law that gave Big Pharma a “get out of jail free” card, which took away all legal and financial liabilities for their defective products, e.g., vaccines.
By the way, there will be the “Empty Stroller Walk” March 5, 2017 around the country to commemorate babies who died after receiving vaccinations. More information about it can be found at Change.Org
Let’s stop the tap dancing around vaccine issues; it’s time for serious action by the U.S. Congress.
Catherine J Frompovich (website) is a retired natural nutritionist who earned advanced degrees in Nutrition and Holistic Health Sciences, Certification in Orthomolecular Theory and Practice plus Paralegal Studies. Her work has been published in national and airline magazines since the early 1980s. Catherine authored numerous books on health issues along with co-authoring papers and monographs with physicians, nurses, and holistic healthcare professionals. She has been a consumer healthcare researcher 35 years and counting.
Why The Only Thing Influenza May Kill Is Germ Theory
Groundbreaking research indicates that nearly everything we once believed about the purportedly deadly properties of flu virus may be based on institutionalized superstition and myth.
Germ theory is an immensely powerful force on this planet, affecting everyday interactions from a handshake, all the way up the ladder to national vaccination agendas and global eradication campaigns. But what if fundamental research on what exactly these ‘pathogens’ are, how they infect us, has not yet even been performed? What if much of what is assumed and believed about the danger of microbes, particularly viruses, has completely been undermined in light of radical new discoveries in microbiology?
Some of our readers already know that in my previous writings I discuss why the “germs as our enemies” concept has been decimated by the relatively recent discovery of the microbiome. For background, feel free to read “How The Microbiome Destroyed the Ego, Vaccine Policy, and Patriarchy.”
In today’s article, I will take a less philosophical approach, and focus on influenza as a more concrete example of the Copernican-level paradigm shift in biomedicine and life sciences we are all presently fully immersed within, even if many in the establishment have yet to fully acknowledge it.
Deadly Flu Viruses: Vaccinate or Die?
The way health policy makers talk about it today, flu virus is a deadly force, against which all citizens, of all ages 6 months or older, need to take an annual influenza vaccine to protect themselves against, lest they face deadly consequences. Worse, those who hold religious or philosophical objections, or who otherwise conscientiously object to vaccinating, are being characterized as doing harm to others by denying them herd immunity (a concept that has been completely debunked by a careful study of the evidence, or lack thereof). For instance, in the interview below Bill Gates tells Sanjay Gupta that he thinks non-vaccinators “kill children”:
But what if I told you that there isn’t even such a thing as “flu virus,” in the sense of a monolithic, disease vector existing outside of us, conceived as it is as the relationship of predator to prey?
First, consider that the highly authorative Cochrane collaboration acknowledges there are many different flu viruses that are not, in fact, influenza A — against which flu vaccines are targeted — but which nonetheless can contribute to symptoms identical to those attributed to influenza A:
“Over 200 viruses cause influenza and influenza-like illness which produce the same symptoms (fever, headache, aches and pains, cough and runny noses). Without laboratory tests, doctors cannot tell the two illnesses apart. Both last for days and rarely lead to death or serious illness. At best, vaccines might be effective against only Influenza A and B, which represent about 10% of all circulating viruses.” (Source: Cochrane Summaries).” [emphasis added]
This makes for a picture of complexity that powerfully undermines health policies that presuppose vaccination equates to bona fide immunity, and by implication, necessitates the herd collectively participate in the ritual of mass vaccination campaigns as a matter of social responsibility and necessity.
Even the use of the word “immunization” to describe vaccination is highly misleading. The moment the word is used, it already presupposes efficacy, and makes it appear as if non-vaccinators are anti-immunity, instead of what they actually are: pro-immunity (via clean air, food, water, and sunlight), but unwilling to subject themselves or their healthy children to “unavoidably unsafe” medical procedures with only theoretical benefits.
Why Flu Virus Doesn’t Exist (The Way We Were Told)
But the topic gets even more interesting when we consider the findings of a 2015 study entitled “Conserved and host-specific features of influenza vision architecture.” This was the first study ever to plumb the molecular depths of what influenza virus is actually composed of. Amazingly, given the long history of vaccine use and promotion, the full characterization of what proteins it contains, and where they are derived from, was never previously performed. How we invest billions of dollars annually into flu vaccines, and have created a global campaign to countermand a viral enemy, whose basic building blocks we don’t even know, is hard to understand. But it is true nonetheless.
The study abstract opens with this highly provocative line:
“Viruses use virions to spread between hosts, and virion composition is therefore the primary determinant of viral transmissibility and immunogenicity.” [emphasis added]
Virion are also known as “viral particles,” and they are the means by which viral nucleic acids are able to move and ‘infect’ living organisms. Without the viral particle (taxi) to carry around the virus DNA (passenger), it would be harmless; in fact, viruses are often described as existing somewhere between living and inanimate objects for this reason: they do not produce their own energy, nor are transmissable without a living host. And so, in this first line, the authors are making it clear that virion composition is also the primary determinant in how or whether a virus is infectious (transmits) and what affects it will have in the immune system of the infected host.
Influenza viral particles.
This distinction is important because we often think of viruses as simply pathogenic strings of DNA or RNA. The irony, of course, is that the very things we attribute so much lethality to — viral nucleic acids — are not even alive, and can not infect an organism without all the other components (proteins, lipids, extra-viral nucleic acids) which are, technically, not viral in origin, participating in the process. And so, if the components that are non-viral are essential for the virus to cause harm, how can we continue to maintain that we up against a monolithic disease entity “out there” who “infects” us, a passive victim? It’s fundamentally non-sensical, given these findings. It also clearly undermines the incessant, fear-based rhetoric those beholden to the pro-vaccine use to coerce the masses into undergoing the largely faith-based rite of vaccination.
Let’s dive deeper into the study’s findings…
The next line of the abstract addresses the fact we opened this article with: namely, that there is great complexity involved at the level of the profound variability in virion composition:
“However, the virions of many viruses are complex and pleomorphic, making them difficult to analyze in detail”
But this problem of the great variability in the virion composition of influenza is exactly why the study was conducted. They explain:
“Here we address this by identifying and quantifying viral proteins with mass spectrometry, producing a complete and quantifiable model of the hundreds of viral and host-encoded proteins that make up the pleomorphic virions of influenza virus. We show that a conserved influenza virion architecture, which includes substantial quantities of host proteins as well as the viral protein NSI, is elaborated with abundant host-dependent features. As a result, influenza virions produced by mammalian and avian hosts have distinct protein compositions.”
In other words, they found that the flu virus is as much comprised of biological material from the host the virus ‘infects,’ as the viral genetic material of the virus per se.
How then, do we differentiate influenza virus as fully “other”? Given that it would not exist without “self” proteins, or those of other host animals like birds (avian) or insects, this would be impossible to do with any intellectual honesty intact.
There’s also the significant problem presented by flu vaccine production. Presently, human flu vaccine antigen is produced via insects and chicken eggs. This means that the virus particles extracted from these hosts would contain foreign proteins, and would therefore produce different and/or unpredictable immunological responses in humans than would be expected from human influenza viral particles. One possibility is that the dozens of foreign proteins found within avian influenza could theoretically produce antigens in humans that cross-react with self-structures resulting in autoimmunity. Safety testing, presently, does not test for these cross reactions. Clearly, this discovery opens up a pandora’s box of potential problems that have never sufficiently been analyzed, since it was never understood until now that “influenza” is so thoroughly dependent upon a host for its transmissability and immunogenecity.
Are Flu Viruses Really “Hijacked” Exosomes?
Lastly, the study identified something even more amazing:
“Finally, we note that influenza virions share an underlying protein composition with exosomes, suggesting that influenza virions form by subverting micro vesicle” production.”
What these researchers are talking about is the discovery that virion particles share stunning similarities to naturally occurring virus-like particles produced by all living cells called exosomes. Exosomes, like many viruses (i.e. enveloped viruses) are enclosed in a membrane, and are within the 50-100 nanometer size range that viruses are (20-400 nm). They also contain biologically active molecules, such as proteins and lipids, as well as information-containing ones like RNAs — exactly, or very similar, to the types of contents you find in viral particles.
Watch this basic video on exosomes to get a primer:
In light of this post-Germ Theory perspective, viruses could be described as pieces of information in search of chromosomes; not inherently “bad,” but, in fact, essential for mediating the genotype/phenotype relationship within organisms, who must adapt to ever-shifting environmental conditions in real-time in order to survive; something the glacial pace of genetic changes within the primary nucleotide sequences of our DNA cannot do (for instance, it may take ~ 100,000 years for a protein-coding gene sequence to change versus seconds for a protein-coding gene’s expression to be altered via modulation via viral or exosomal RNAs).
This does not mean they are “all good,” either. Sometimes, given many conditions outside their control, their messages could present challenges or misinformation to the cells to which they are exposed, which could result in a “disease symptom.” But with the caveat that these disease symptoms are often if not invariably attempts by the body to self-regulate and ultimately improve and heal itself.
In other words, the virion composition of viruses appears to be the byproduct of the cell’s normal exosome (also known as microvessicle) production machinery and trafficking, albeit being influenced by influenza DNA. And like exosomes, viruses may be a means of extracellular communication between cells, instead of simply a pathological disease entity. This could explain why an accumulating body of research on the role of the virome in human health indicates that so-called infectious agents, including viruses like measles, confer significant health benefits. [see: the Health Benefits of Measles and The Healing Power of Germs?].
Other researchers have come to similar discoveries about the relationship between exosomes and viruses, sometimes describing viral hijacking of exosome pathways as a “Trojan horse” hypothesis. HIV may provide such an example.
Concluding Remarks
The remarkably recent discovery of the host-dependent nature of the influenza virus’ virion composition is really just the tip of an intellectual iceberg that has yet to fully emerge into the light of day, but is already “sinking” ships; paradigm ships, if you will.
One such paradigm is that germs are enemy combatants, and that viruses serve no fundamental role in our health, and should be eradicated from the earth with drugs and vaccines, if possible.
This belief, however, is untenable. With the discovery of the indispensable role of the microbiome, and the subpopulation of viruses within it — the virome — we have entered into an entirely new, ecologically-based view of the body and its environs that are fundamentally inseparable. Ironically, the only thing that influenza may be capable of killing is germ theory itself.
For an in-depth exploration of this, watch the lecture below on the virome. I promise, if you do so, you will no longer be able to uphold germ theory as a monolithic truth any longer. You may even start to understand how we might consider some viruses “our friends,” and why we may need viruses far more than they need us.
Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of GreenMedInfo or its staff.
TheBreakAway 