Your Own Operating System

Dr. David Martin on Experimental mRNA COVID Vaccines: This is NOT a Vaccine! It is a Medical Device

Dr. David Martin. Image Source.

by Brian Shilhavy
Editor, Health Impact News

Recently Sasha Stone hosted a 2 hour live stream event called “Focus on Fauci.” Participating in the event were Dr. Rocco Galati, Dr. David Martin, Dr. Judy Mikovits, and Robert F. Kennedy Jr.

Dr. Martin has made tidal waves in the Alternative Media since this event, by explaining that the experimental mRNA COVID vaccines are not even vaccines, and legally cannot be called “vaccines,” because they are really medical devices.

Dr. Martin should be familiar to readers of Health Impact News (as are the other participants), as he was the featured scientist in filmmaker Mikki Willis’ excellent production: Plandemic. He exposed, for example, how the U.S. Government has owned patents on coronaviruses since the 1990s.

Here is a partial bio of Dr. David Martin from his website:

His first invention was a laser integrated system to target and treat inoperable tumors. His mathematics helped unravel the way the human body processes hormones and led to the detection and treatment of many diseases.

His observation of human behavior led to his development of technology which deciphers the intention and motivation of communication – a technology that has impacted and saved the lives of billions.

His global business activities served to develop the world’s top-performing global equity index (including the CNBC IQ100 powered by M·CAM).

He’s brought the world’s largest white-collar criminals to justice and brought the world’s most oppressed and disenfranchised transformative ways to engage.

From the starry expanses of Mongolia to the flashing lights of New York, his work is as passion-filled whether it’s with a camel herder or a global CEO. (Source.)

“This is not a vaccine.”

Here is a partial transcript of the video below explaining that the mRNA vaccines are not really vaccines:

This is not a vaccine.

We need to be really clear. We’re using the term “vaccine” to sneak this thing under public health exemptions.

This is not a vaccine. This is an mRNA packaged in a fat envelope, that is delivered to a cell.

It is a medical device designed to stimulate the human cell into becoming a pathogen creator.

It is not a vaccine. Vaccines actually are a legally defined term, and they’re a legally defined term under public health law, they’re legally defined term under the CDC and FDA standards.

And a vaccine specifically has to stimulate both an immunity within the person who is receiving it, but it also has to disrupt transmission.

And that is not what this is. They have been abundantly clear in saying that the mRNA strand that is going into the cell, it is not to stop transmission. It is a treatment.

But if it was discussed as a treatment, it would not get the sympathetic ear of the public health authorities, because then people would say, well what other treatments are there?

Watch the full explanation by Dr. Martin below.

The entire 2.5 hour event can be viewed here on Bitchute.

And just a reminder, Moderna themselves have admitted that the mRNA injections are an Operation System, the “Software of Life.”

The New mRNA COVID Vaccines Inject an Operating System into Your Body – Not a Conspiracy Theory, Moderna Admits It

Comment on this article at HealthImpactNews.com.

from:   https://vaccineimpact.com/2021/dr-david-martin-on-experimental-mrna-covid-vaccines-this-is-not-a-vaccine-it-is-a-medical-device/

 

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Some Info on Covid Vaccines

COVID-19 VACCINES IMPORTANT POINTS
Please Share with Your Family and Friends

MINOR IMPACT: Vaccine manufacturers claim that Covid-19 vaccines are 95 percent “effective,” but the FDA is allowing companies to define effectiveness as “prevention of mild symptoms.” The studies are not designed to detect a reduction in outcomes such as severe illness, hospitalization or death.(1,2)   For individuals who develop severe symptoms, the vaccine is not a remedy. Instead, nutritional and oxidative support can help keep the illness from going into “overdrive.”(3)

EXPECT ADVERSE REACTIONS: Participants in every Covid-19 vaccine trial have reported adverse reactions including high fever, chills, muscle pains and headaches. (4-6) Some have even reported severe reactions that required hospitalization and invasive treatment. According to the FDA, potential long-term effects may include Guillain-Barré syndrome, brain swelling, muscle weakness and paralysis, convulsions and seizures, stroke, narcolepsy, shock, heart attack, autoimmune disease, arthritis and joint pain, multisystem inflammatory syndrome in children, and death.(7)   Some UK health workers have experienced anaphylactic shock after receiving one dose of the approved vaccine.8

WON’T PREVENT COVID-19: An FDA Pfizer briefing paper published December 10, 2020 revealed 43 percent more suspected cases of Covid-19 in the vaccinated group than in the placebo group within seven days of vaccination.(9)

NO LIABILITY: Covid-19 vaccine manufacturers will be protected from all liability—if you are injured, you cannot sue. (10) Manufacturers will have complete indemnity even though all previous attempts at creating coronavirus vaccines caused harm and never advanced to regulatory approval. (11)

WILL NOT END RESTRICTIVE MEASURES: Dr. Anthony Fauci of the National Institutes of Health acknowledges that the vaccines may prevent symptoms but will not block spread of the virus, so vaccine recipients will still need to wear masks, practice social distancing and avoid crowds. (12,13)

NOT NECESSARY: According to the CDC’s current best estimate, the “infection fatality rate” (IFR) for Covid-19 is less than 1 percent for people age 69 and younger, including a .003 percent IFR for children and adolescents. (14)

COULD MAKE YOU STERILE: Two prominent doctors, including the ex-head of Pfizer’s respiratory research, warn that Covid-19 vaccines contain a spike protein called syncytin-1, vital for the formation of the placenta.15 If the vaccine triggers an immune response to this protein, then female infertility, miscarriage or birth defects could result.

FOR FURTHER INFORMATION (including printable flyers): https://www.westonaprice.org/covid-19-vaccines-important-points/

1.        Doshi P. Will covid-19 vaccines save lives? Current trials aren’t designed to tell us. BMJ. 2020;371:m4037. https://www.bmj.com/content/371/bmj.m4037.
2.        Haseltine WA. Covid-19 vaccine protocols reveal that trials are designed to succeed. Forbes, September 23, 2020. https://www.forbes.com/sites/williamhaseltine/2020/09/23/covid-19-vaccine-protocols-reveal-that-trials-are-designed-to-succeed/?sh=5da0663d5247.
3.        Brownstein D, Ng R, Rowen R et al. A novel approach to treating COVID-19 using nutritional and oxidative therapies. Science, Public Health Policy, and the Law. 2020;2:4-22. https://ozonewithoutborders.ngo/wp-content/uploads/2020/07/Novel-Approach-to-Covid-19.pdf.
4.        Jackson LA, Anderson EJ, Rouphael NG et al. An mRNA vaccine against SARS-CoV-2 – preliminary report. New England Journal of Medicine. 2020;383(20):1920-1931. https://www.nejm.org/doi/full/10.1056/NEJMoa2022483.
5.        Allen A, Szabo L. NIH “very concerned” about serious side effect in coronavirus vaccine trial. Scientific American, September 15, 2020. https://www.scientificamerican.com/article/nih-very-concerned-about-serious-side-effect-in-coronavirus-vaccine-trial/.
6.        Mayer A. Leading COVID vaccine candidates plagued by safety concerns. The Defender, November 13, 2020. https://childrenshealthdefense.org/defender/covid-vaccine-candidates-safety-concerns/?itm_term=home. .
7.        U.S. Food and Drug Administration. Vaccines and Related Biological Products Advisory Committee, October 22, 2020 Meeting Presentation, slide #16. https://www.greenmedinfo.com/blog/covid-19-vaccine-bombshell-fda-documents-reveal-death-21-serious-conditions-possi1.
8.        Reals T. U.K. warns against giving Pfizer vaccine to people prone to severe allergic reactions. CBS News, December 9, 2020. https://www.cbsnews.com/amp/news/covid-vaccine-pfizer-shot-uk-warning-people-with-history-of-significant-allergic-reactions/#app.
9.        https://www.fda.gov/media/144245/download, page 42.
10.    Public Readiness and Emergency Preparedness Act. COVID-19 PREP Act Declarations. https://www.phe.gov/Preparedness/legal/prepact/Pages/default.aspx.
11.    Lyons-Weiler J. Pathogenic priming likely contributes to serious and critical illness and mortality in COVID-19 via autoimmunity. Journal of Translational Autoimmunity. 2020;3:100051. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142689/.
12.    Khemlani A. Fauci: Early COVID-19 vaccines will only prevent symptoms, not block the virus. Yahoo! Finance, October 26, 2020. https://finance.yahoo.com/news/fauci-vaccines-will-only-prevent-symptoms-not-block-the-virus-195051568.html.
13.    Scipioni J. Dr. Fauci says masks, social distancing will still be needed after a Covid-19 vaccine—here’s why. CNBC, November 16, 2020. https://www.cnbc.com/2020/11/16/fauci-why-still-need-masks-social-distancing-after-covid-19-vaccine.html.
14.    Centers for Disease Control and Prevention. COVID-19 pandemic planning scenarios. Updated September 10, 2020. https://www.cdc.gov/coronavirus/2019-ncov/hcp/planning-scenarios.html.
15.    Petition/motion for administrative/regulatory action regarding confirmation of efficacy end points and use of data in connection with the following clinical trials. Dr. Wolfgang Wodarg and Dr. Michael Yeadon, petitioners. Filed with European Medicines Agency, December 1, 2020. https://healthimpactnews.com/wp-content/uploads/sites/2/2020/12/Wodarg_Yeadon_EMA_Petition_Pfizer_Trial_FINAL_01DEC2020_EN_unsigned_with_Exhibits.pdf.
: Vaccine manufacturers claim that Covid-19 vaccines are 95 percent “effective,” but the FDA is allowing companies to define effectiveness as “prevention of mild symptoms.” The studies are not designed to detect a reduction in outcomes such as severe illness, hospitalization or death.1,2 For individuals who develop severe symptoms, the vaccine is not a remedy. Instead, nutritional and oxidative support can help keep the illness from going into “overdrive.”3

A Little Shot of Cancer, Perhaps?

(Please note that I have excerpted a good deal of the text which is available at the link below)

Sausage Making at FDA: How Human Cancer Cells Got Into Vaccines

In a 2012 meeting, the FDA voted to allow the use of human fetal cells and adult human tumor cells in vaccines, despite acknowledging the many risks, including that vaccine recipients might later develop cancer.

“If the American people knew some of the things that went on at the FDA, they’d never take anything but Bayer aspirin.” — Len Lutwalk, FDA scientist

“The FDA, by spinelessly knuckling under to every whim of the drug companies, has thrown away its high reputation, and in doing so, forfeited our trust.” — Drummond Rennie, deputy editor of JAMA


Vaccines and related biological products advisory committee today

Today — Thursday, Dec. 10 — the Vaccines and Related Biological Products Advisory Committee (VRBPAC), which is the U.S. Food and Drug Administration’s (FDA) internal panel that licenses new vaccines as “safe and effective,” will meet to consider Pfizer’s COVID vaccine. VRBAC will meet in one week, Dec. 17, to consider approval of the Moderna vaccine.

The damning safety studies in Pfizer’s late release clinical trial data dump, and the severe (life-threatening) allergic reactions that bedeviled the vaccine’s UK rollout, have raised red flags and public anxiety about the safety of the companies’ mRNA vaccines. Anthony Fauci has addressed growing skepticism about COVID vaccines and the Operation Warp Speed program, by reassuring the public that “VRBPAC” is an “independent panel of leading experts” whom the public can absolutely trust to assure vaccine safety.

How FDA originally approved use of fetal cells in vaccines

FDA allows both human fetal cells and adult human tumor cells in vaccines. Both types have cancer risks. While both Pfizer and Moderna tested their mRNA vaccine using fetal cells, there are no fetal cells, cell debris or DNA in their final products.

However, according to company documents, Johnson and Johnson (Janssen) and Altimmune’s COVID vaccines are manufactured in the human fetal cell line PER-C6, and thus the final vaccine products will contain cellular debris and DNA fragments from these cells. Researchers harvested these cell lines from the eyeball of an 18-week-old human fetus aborted in 1985, and then rendered them immortal by making them cancerous.

The AstraZeneca, Cansino, Gamayela, Vaxart, LongComm and Upitt vaccines are manufactured in the human fetal cell line HEK293, and thus the final vaccine products will contain cellular debris and DNA fragments from the fetal HEK-293 cell line. Scientists harvested this cell line from the kidney of a female Dutch fetus legally aborted in 1973 and then immortalized the cells by rendering them cancerous.

Normal primary cells, which are unable to replicate indefinitely, ultimately die. Immortalized cell lines are derived from known malignant cancer cells such as those obtained from Henrietta Lacks (HeLa) or created in the laboratory by introducing viral oncogenes or chemical exposures capable of mutating normal primary cells into immortal tumor cells.

According to FDA’s “The Pink Sheet” dated Nov. 29, 1999, for two decades the agency has been acutely aware of the inherent risks of using immortalized cell lines for vaccine development. The FDA CBER Director Dr. Peter Patriarca, M.D. explained that continuous cell lines are used for their ability to self-propagate, making them an ideal substrate on which to grow viruses, “the worst thing we are concerned about is …  malignancy, because some of these continuous cells have the potential for growing tumors in laboratory animals.”

Patriarca further conceded that “the technology to make these vaccines actually exceeds the science and technology to understand how these vaccines work and to predict how they will work.”   …

We call vaccines “biologics” because vaccinologists have traditionally grown their antigens on biological substrates — usually animal tissue. Competing companies culture COVID vaccines on a variety of animal strata. The Merck and IAVA COVID vaccines are manufactured in vero monkey cells, and thus contain cellular debris and DNA fragments from vero monkeys in the final product. The Sanofi, GSK, and Novavax COVID jabs are manufactured in insect cells and thus contain insect cellular debris and DNA fragments in the final products.

Public health advocates criticize the use of animal tissues in vaccines due to risks that they carry endogenous viruses, microbes, parasites and lack safety testing. (Plague of Corruption, Mikovits 2020). …

Researchers and regulatory agencies have worried for more than 50 years about the potential for injected DNA to cause cancer.  …

Regulators have in the past predicted that the odds of that happening were less than 1 in a trillion. However, in early gene therapy trials this event did indeed occur in 4 of 9 boys, 1 of whom died from the leukemia the insertions caused.

FDA as an arm of Big Pharma

Between 2000 and 2010, pharmaceutical companies paid the FDA $3.4 billion to gain rapid drug approvals. Today, Pharma companies underwrite three-quarters of FDA’s budget for scientific reviews (ProPublica) and fund nearly 50% of the FDA’s total annual budget through PDUFA fees. In exchange, the agency increasingly fast-tracks expensive drugs and vaccines with significant side effects and unproven health benefits.

Corrupt vaccine approval panels

But as corrupt as FDA is, the internal panels — VRBAC — that approve new vaccines make the rest of the agency look like a Sunday church picnic.

When Dr. Fauci, Paul Offit, Peter Hotez and Bill Gates tell you that you needn’t worry because FDA is the “gold standard” for vaccine safety and that the ultimate licensing decision will be made by an “independent panel of experts,” they are talking about VRBPAC. But VRBPAC is far from “independent.” It is not even comprised exclusively of public officials. Instead, it is populated by outside “experts” who are almost all pharmaceutical industry insiders.

In 2003, following a 3-year investigation, the United States Congress’s House Oversight Committee found VRBAC was completely dominated by the vaccine industry.

“Examples of Conflicts of Interest:

  1. “For instance, 3 out of 5 FDA advisory committee (VRBPAC) members who voted to approve the rotavirus vaccine in December 1997 had financial ties to pharmaceutical companies that were developing different versions of the vaccine.
  2. “One out of five voting members’ employer had a $9,586,000 contract for a rotavirus vaccine.
  3. “One out of five voting members was the principal investigator for a Merck grant to develop a rotavirus vaccine.
  4. “One out of five voting members received approximately $1 million from vaccine manufacturers toward vaccine development.”

Congressional investigators concluded that, “Altogether, four out of the five committee members had conflicts of interest that required waivers, and their recommendation for approval of the vaccine was unanimous.”

Here’s what happened at the 2012 FDA meeting on fetal cells

HHS acknowledges that the FDA and Centers for Disease Control committees that contract and review new vaccines have historically not used “evidence-based medicine.” To illustrate what this means, one only need read (below) the astonishing transcript of the 2012 panel that first approved the use of adult cancer tumor cells in vaccines.

This transcript shows what the public is never supposed to see: the behind-the-scenes sausage-making of federal vaccine approvals. Here, you will read for yourself how the “independent,” “gold standard” panelists entrusted with protecting your children made monumentally consequential decisions, not on evidence-based science, but by rolling the dice and taking what they knew was a horrendously risky bet on public health

In any other realm, this transcript would be proof of negligent homicide. … We are all lab rats in their high-risk population-wide experiment. At FDA’s vaccine division, that sort of reckless decision-making is routine.

In 2012, most live virus vaccines were from animal tissue and the idea of putting potentially cancerous tumor cells from adult “donors” in vaccines was still a daring and audacious gamble. That September, the FDA VRBPAC committee met to discuss this risky innovation. The transcript of that meeting — showing captive FDA officials considering a proposal by the pharma cabal to allow the use of human cancer cells (HeLa) to replace animal tissue in the manufacture of vaccines — is proof of reckless criminal conduct.

The HeLa cells are well known to cause cancer in animals, but Big Pharma wanted to lower production costs of vaccines and this method is cheaper and faster than using animal tissue for the cultivated media. …

Unbelievably, FDA voted to allow pharmaceutical companies to produce vaccines using human cells without reviewing a single scientific study to determine if the outcome would be safe.

Before, I quoted some of the criminally reckless statements from the meeting directly. A more detailed account appears in this article.

This was a full meeting of FDA’s VRBPAC in 2012 to decide on the use of human tumor cell lines for the production of vaccines. I list these speakers and their titles at that time:

  • Dr. Philip Krause, Acting Deputy Director of OVRR (Office of Vaccine Research and Review) and FDA’s CBER (Center for Biologics Evaluation and Research). Also, Principal Investigator for Vaccine Safety: Virus Detection and Latency.
  • Dr. Doug Lowy, Director of the National Cancer Institute of the NIH.
  • Dr. Robert Daum, Chair of the VRBPAC.
  • Donald W. Jehn M.S., Designated Federal Officer for VRBPAC.
  • Keith Peden, PhD, Chief of LDNAV, DVP/OVRR/CBER.
  • Dr. Marion Gruber, Director of the FDA’s Office of Vaccines.
  • Dr. Nathanial Brady, a self-described clinician.
  • Dr. Pamela McInnes, a vaccine development expert and the Director of the Division of Extramural Research at the NIH’s National Institute of Dental and Craniofacial Research, and previously a Deputy Director under Anthony Fauci at the National Institute of Allergy and Infectious Diseases.

Pharma knew that their tumorigenic vaccines might cause tumors in recipients.

FDA officials knew that tumors might occur decades after vaccination.

FDA openly acknowledged that its primary objective was not to assure public safety but to help vaccine manufacturers.

FDA officials knew that they could not prove vaccine safety using test animals to assess oncogenicity.

FDA officials deliberately terminated animal safety tests too early in order to conceal consequences.

FDA decided to keep the tumor cell lines secret, because doctors and the public may be alarmed and say “Oh, my God!” if they knew the truth.

FDA decided to use deceptive language to convince doctors and the public that the vaccines were safe even when they, themselves, were unconvinced of safety.

FDA decided to hide information about their use of tumor cells and omit it from package inserts. 

Health authorities were skeptical about safety of the tumor lines, but they decided to subject the public to the risk, so that they could perform a global population-wide live human experiment.

FDA officials opted to toss the dice, perform the population-wide human experiment, and learn about the risks as time goes by.

The committee formally approves the method of making vaccines from human cancer tumors.

..

Prior to voting to go forward, the committee made the following conclusions:

  • Making vaccines with cells that are directly derived from human cancer tumors is faster and cheaper than breeding animals for the culture media.
  • Millions of potentially cancer-causing vaccines will be produced.
  • The vaccines may possibly cause genetic mutations.
  • Millions of dollars will be made by vaccine promoters.
  • The health of millions of consumers may be jeopardized.
  • Information about how vaccines are made will be hidden from doctors and

Finally, it’s worth considering that cancer treatment drugs like Keytruda are among pharmaceutical companies’ largest profit makers. Precipitating a cancer epidemic in human populations only benefits vaccine makers’ bottom line.

Remember, these are the same companies and the same FDA regulators that brought us the opioid epidemic.

from:    https://childrenshealthdefense.org/defender/fda-cancer-cells-in-vaccines/?utm_source=salsa&eType=EmailBlastContent&eId=8fc80363-cace-4de1-bcd2-9e309b779ac5

Rethinking Viruses

Why Everything You Learned About Viruses is WRONG

By Sayer Ji

Contributing writer for Wake Up World

Groundbreaking research indicates that most of what is believed about the purportedly deadly properties of viruses like influenza is, in fact, not evidence-based but 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 in depth background on this topic, read my previous article, “How The Microbiome Destroyed the Ego, Vaccine Policy, and Patriarchy.” You can also read Profound Implications of the Virome for Human Health and Autoimmunity, to get a better understanding of how viruses are actually beneficial to mammalian health.

In this 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 the medical establishment has yet to acknowledge it. (a topic I cover extensively in my book REGENERATE: Unlocking Your Body’s Radical Resilience through the New Biology).

Deadly Flu Viruses: Vaccinate or Die?

The hyperbolic manner in which health policymakers and mainstream media pundits talk about it today, flu virus (or COVID-19) is an inexorably lethal force (note: viruses are obligiate parasites, at worst, with no inner motive force to actively “infect” others), against which all citizens, of all ages 6 months or older, need the annual influenza vaccine to protect themselves against, lest they (it is said) 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 life-or-death social 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 virion 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 were not even known until a few years ago, 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]

Influenza viral particles

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 effects it will have in the immune system of the infected host.

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 are 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 stance 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:

When we start to look at viruses through the lens of their overlap with exosomes, which as carriers of RNAs are essential for regulating the expression of the vast majority of the human genome, we start to understand how their function could be considered neutral as “information carriers,” if not beneficial. Both exosomes and viruses may actually be responsible for inter-species or cross-kingdom communication and regulation within the biosphere, given the way they are able to facilitate and mediate horizontal information transfer between organisms. Even eating a piece of fruit containing these exosomes can alter the expression of vitally important genes within our body.

Exosomes

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.” 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 microvesicle) 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.

from:   https://wakeup-world.com/2020/09/03/why-everything-you-learned-about-viruses-is-wrong-2/

What’s Going On – Part 5

This Is The “Sh*t Hitting The Fan” Part Of The Fourth Turning

by Tyler Durden

Authored by Jim Quinn via The Burning Platform blog,

When pondering the possible outcomes of this Fourth Turning, we tend to be drawn towards the negative, because a positive outcome seems so unlikely given the current animosity roiling the country. If you step back and realize all the hate and conflict is being engineered and coordinated by a ruling class of powerful rich men, then average Americans could organize a new paradigm that honors the original intent of the U.S. Constitution, allowing citizens the liberty and freedom to create voluntary associations based upon common interests at a local level.

The ruling oligarchs find this unacceptable, so this freedom must be wrested away from them by any means necessary. There is a civil war already underway, but only one side is fighting – the billionaire class who not only don’t want to relinquish some power, but want total control over every aspect of our lives. I believe this election will turn this one-sided silent war into a hot war.

Rather than wallowing in doom and the worst-case scenarios, we should be trying to figure out how to reorganize our nation going forward, after the billionaire oligarchs are defeated. As I was trying to go back in time to see when I wrote my first Fourth Turning article, I came across an article I wrote in 2010 – Brave New World 2010.

At the end of the article I noted the wisdom and practicality of Aldous Huxley’s advice on how to restructure our society, from his 1958 book Brave New World Revisited. This should be a template for restructuring our way of life if we want a sustainable future. I am not optimistic we have the fortitude, wisdom, courage and will to choose Huxley’s suggested path:

  • As recent history has repeatedly shown, the right to vote, by itself, is no guarantee of liberty. Therefore, if you wish to avoid dictatorship by referendum, break up modern society’s merely func­tional collectives into self-governing, voluntarily cooperating groups, capable of functioning outside the bureaucratic systems of Big Business and Big Govern­ment.
  • If you wish to avoid the spiritual impoverishment of individuals and whole societies, leave the metropolis and revive the small country community, or alternately humanize the me­tropolis by creating within its network of mechanical organization the urban equivalents of small country communities, in which individuals can meet and co­operate as complete persons, not as the mere embodi­ments of specialized functions.

Huxley’s prescription of re-humanizing our country and voluntarily choosing where we want to live and who we want to associate with in small enclaves is how many rural communities already function. We can either willingly choose this path peacefully, or we will be left with this as our only option after our modern world self-destructs during the violent cataclysm, following the crashing of our Ponzi scheme debt saturated economic system.

The American Empire is clearly in rapid decline and may not survive the trials and tribulations over the coming decade. The Fourth Turning is not a prophecy, but should be taken as a warning and call to action. Sitting this out and hoping for the best will not help achieve a positive outcome. Tragedy or triumph – the choices we make will matter. The climax of this Fourth Turning may be a few years off, but the battle for the soul of America begins on November 3.

“History offers no guarantees. Obviously, things could go horribly wrong – the possibilities ranging from a nuclear exchange to incurable plagues, from terrorist anarchy to high-tech dictatorship. We should not assume that Providence will always exempt our nation from the irreversible tragedies that have overtaken so many others: not just temporary hardship, but debasement and total ruin. Losing in the next Fourth Turning could mean something incomparably worse. It could mean a lasting defeat from which our national innocence – perhaps even our nation – might never recover.” – Strauss & Howe – The Fourth Turning

from:    https://www.zerohedge.com/geopolitical/sht-hitting-fan-part-fourth-turning

A Few Considerations

Times of crisis often, although not inevitably, lead to times of awakening.
The lack of inevitability is a function of the minds (and spirits/souls) of individuals and their inclination towards the light or the darkness.
The physical separation of people has the effect of isolating many in their own mind sets which can be a rabbit hole all of itself.
And then these group uprisings, many of which are questionable in terms of the participants, are a major distraction in the news which will further polarize the country.
These things are, after all, tools used by the Uber-PTB, and by that I am referring to the ones over those who feel themselves to be the Powers That Be, who are the pawns who merely arrange the pieces as they are instructed— they are the tools used to achieve the end they have in sight.
There is also the ET factor, which definitely plays into the process we now see unfolding, a factor that can mean the further control of the human population.
But the spiritual movement towards awakening is a force that is motivating many, and hopefully the group energetics of light that are moving upward will calm the waters and  bring some clarity.

Those Who Do Not Learn From History…

ARE FORCED TO REPEAT IT:
And now to the article:
alternative news

BACK TO SQUARE ONE: THE POLIO VACCINE… AGAIN…

September 6, 2020 By Joseph P. Farrell

L.G.L.R., and A.F. both sent this article along (and a thank you to both), and I had to sit up and take notice, because this one hits close to home, so to speak. Like many people my age, I was vaccinated as a child with the polio vaccine. In fact, it was the only vaccine my parents ever consented to allow me to take.

But that was not until after they had both done a little ‘digging”. At the time – the late fifties and early sixties – polio was still a killer if not a major crippler. Pictures of unfortunate people in iron lungs were still in the newspapers, and the disease was never far from our minds. My parents, of course, were the children of the depression era, and remembered the stories of President Franklin Roosevelt and his struggle with the disease. Say what one will about his policies (and I have a lot to say about them, and very little of it is good), one certainly cannot fault the man for waging a courageous struggle against the disease, including forcing himself to stand and walk, probably in a great deal of pain, and certainly with a great deal of effort, to give those speeches in front of Congress, or to meet on British battleships with Prime Minister Churchill. When it came to me, there were two choices of a polio vaccine then: the Salk vaccine (the first one out of the gate), and the Sabin vaccine.

The Salk vaccine actually caused vaccine-induced polio in a number of cases, and quickly became controversial, in part, because it was being pushed by the US government and state and local governments (sound familiar?). THe reason for the paralysis? The pharmaceutical company that had been the source for the vaccine had not adequately de-activated the virus in the vaccine, and hence, many children were injected with the real thing (sound familiar?).

The other alternative was the Sabin vaccine, administered orally in a sugar cube, and first extensively tested in Mexico and the Soviet Union. Because of the mess caused by the Salk vaccine, the Sabin vaccine became the vaccine of choice, including for my parents after consultation with their, and my, doctor.

I mention all this, because in the article L.G.L.R. and A.F. both sent me, polio vaccines are again in the news, and are again apparently causing some havoc:

UN Forced To Admit Gates-Funded Vaccine Is Causing Polio Outbreak In Africa

There’s a few details here worth noting:

This really should be one of the biggest scandals in public health, but it’s given little attention – mainly because of the high-profile nature of the people and organisations involved.

The United Nations has been forced to admit that a major international vaccine initiative is actually causing the outbreak of the very disease it was supposed to wipe-out.

While international organisations like the World Health Organization (WHO) will regular boast about supposedly ‘eradicating polio’ with vaccines, the opposite seems to be the case. Their decades-long campaign to eradicate polio is now killing scores of innocent young people living in poor countries.

Now it seems that health officials are beginning to admit that their plan to stop ‘wild’ polio is backfiring, as scores children are being paralyzed a deadly strain of the pathogen derived from a live vaccine – causing a virulent of polio to spread. (All emphases in the original)

A live virus in a polio vaccine… again? Shades of the Salk vaccine episode. One would think that since the 1950s we’d have learned how to kill a virus before putting it into a vaccine (c0vid-19 vaccine enthusiasts, take note!), but apparently we can’t, at least, not with 100% efficiency.

But wait, there’s more:

This latest pharma-induced pandemic has broken out in the African countries of Chad and Sudan, and the culprit has been identified: a vaccine-derived polio virus type 2. Officials now fear this new dangerous strain could soon ‘jump continents,’ causing further deadly outbreaks around the world.

Shocking as it sounds, this Big Pharma debacle is not new. After spending some $16 billion over 30 years to eradicate polio, international health bodies have ‘accidentally’ reintroduced the disease to in Pakistan, Afghanistan, and also Iran, as the central Asia region was hit by a virulent strain of polio spawned by the corporate pharmaceutical vaccine distributed there. Also, in 2019, the government of Ethiopia ordered the destruction of 57,000 vials of type 2 oral polio vaccine (mOPV2) following a similar outbreak of vaccine-induced polio.

It’s important to note that the oral polio vaccine being pushed on to the African population by the Global Polio Eradication Initiative (GPEI), a consortium which is supported and funded by the Bill & Melinda Gates Foundation.

All of this should be a cause for concern, especially with western governments and transnational pharmaceutical giant all rushing to roll-out their new Gates-funded experimental coronavirus vaccine for the global population. (Italicized emphasis added)

The Baal and Malicious Gates Foundation? You don’t say!  Would this be the same folks with unusual ties to some eugenicists in their background, and if that’s the case, is the selection of African tests subjects, in this case, children of poor people in Chad and the Sudan, perhaps not coincidental? Sorry about the digression, they were just a few thoughts and questions that popped into my mind. But another thing just popped into my mind. Is this the same Baal and Malicious Gates that India banned due to the less-than-healthy-results of some vaccine trials there? Gee… I wonder…

The bottom line here, however, is that the vaccination-polio-eradication program has backfired, for the vaccine designed to eradicate it  – which, let us note, is being orally administered in the pictures, and therefore appears to be some sort of update to the Sabin vaccine – is actually introducing more virulent strains into the population. And that in turn might mean that the entire population is once again at risk of the disease, perhaps even including those who, like me, received a vaccine against it as a child.

Gee, thanks alot, Baal, and Malicious.

And lest that misses the point, the article puts it so simple that even a noodnik busybody billionaire can understand it:

This latest revelation from Africa should prompt media and health advocates to ask hard questions about the efficacy and safety of the much-hyped COVID ‘miracle’ vaccine.

Yup. That pretty well says it for me.

See you on the flip side…

from:    https://gizadeathstar.com/2020/09/back-to-square-one-the-polio-vaccine-again/

Appreciate Your Plant Family!

Plants can recognise their relatives, make decisions, and even COUNT, scientists say

  • Prince Charles  was roundly mocked for saying he talked to plants years ago
  • And now it appears plants may be smarter than even the Prince of Wales thought
  • Plants can count, make decisions, recognise relatives and remember events

If  he were that sort of chap, Prince Charles would be within his rights to deliver a right royal ‘I told you so’.

For in the years since he was roundly mocked for saying he talked to plants – and that they ‘responded’ – evidence has grown that he may have been on to something.

And now it appears plants may be smarter than even the Prince of Wales thought.

According to researchers, plants can count, make decisions, recognise their relatives and even remember events.

For in the years since he was roundly mocked for saying he talked to plants ¿ and that they ¿responded¿ ¿ evidence has grown that he may have been on to something. Pictured: Stock photo of houseplants on a window

For in the years since he was roundly mocked for saying he talked to plants – and that they ‘responded’ – evidence has grown that he may have been on to something. Pictured: Stock photo of houseplants on a window

According to researchers, plants can count, make decisions, recognise their relatives and even remember events. Pictured: A gardener pruning a Hibiscus Plant

According to researchers, plants can count, make decisions, recognise their relatives and even remember events. Pictured: A gardener pruning a Hibiscus Plant

And while they may not have a brain, they can learn in a similar way to humans and animals, say scientists.

Professor Umberto Castiello said: ‘Although the idea that plants may behave in a cognitive way may baffle the public, many of us are genuinely amazed by the complexity of plant responses.

‘Evidence is accumulating supporting notions that plants can communicate, remember, decide, and even count – all abilities that one would normally call cognitive if they were observed in animals.’

Professor Castiello said many studies show their cognitive abilities. One found Venus flytraps can ‘count’ the number of steps their prey made.

Scientists observed that the plant trapped prey only when an insect triggered it twice within 20 seconds. This means the plants can remember the first signal for a short time. The reason why plants need to ‘count’ the steps of its prey could be to avoid wasting energy by responding to random raindrops or windblown debris.

Another experiment showed the flowering plant Mimosa pudica can remember being dropped.

The plant was dropped from 6in 60 times in a row and by the end of the experiment it no longer folded its leaves in a defensive response as it realised being dropped from that height would not hurt.

‘The plant “realises” that being dropped is normal,’ Professor Castiello, from the University of Padua in Italy, wrote. ‘More astonishingly, this reflex lasts up to a month which demonstrates the acquisition and expression of a long-lasting memory.’

And shrubs can recognise their kin too as they release more chemicals when planted near their relatives which helps them stave off predators.

It is even thought plants can manipulate competitors when resources are scarce. Plants experiencing a lack of water can share this information with nearby shrubs by sending signals via their roots.

This prompts a nearby plant – its competitor – to start conserving water and this behaviour ultimately benefits both.

Professor Castiello concluded: ‘The question should no longer be if plants are cognitive organisms but how plants make use of their cognitive capacities.’

 

from:    https://www.dailymail.co.uk/sciencetech/article-8680155/Plants-recognise-relatives-make-decisions-COUNT-scientists-say.html