Some Info on Covid Vaccines

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):

1.        Doshi P. Will covid-19 vaccines save lives? Current trials aren’t designed to tell us. BMJ. 2020;371:m4037.
2.        Haseltine WA. Covid-19 vaccine protocols reveal that trials are designed to succeed. Forbes, September 23, 2020.
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.
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.
5.        Allen A, Szabo L. NIH “very concerned” about serious side effect in coronavirus vaccine trial. Scientific American, September 15, 2020.
6.        Mayer A. Leading COVID vaccine candidates plagued by safety concerns. The Defender, November 13, 2020. .
7.        U.S. Food and Drug Administration. Vaccines and Related Biological Products Advisory Committee, October 22, 2020 Meeting Presentation, slide #16.
8.        Reals T. U.K. warns against giving Pfizer vaccine to people prone to severe allergic reactions. CBS News, December 9, 2020.
9., page 42.
10.    Public Readiness and Emergency Preparedness Act. COVID-19 PREP Act Declarations.
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.
12.    Khemlani A. Fauci: Early COVID-19 vaccines will only prevent symptoms, not block the virus. Yahoo! Finance, October 26, 2020.
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.
14.    Centers for Disease Control and Prevention. COVID-19 pandemic planning scenarios. Updated September 10, 2020.
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.
: 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

Nashville DEW

Nashville “Bombing” – Directed Energy Weapon Caught on Camera BEFORE Explosion!

Nashville "Bombing" - Directed Energy Weapon Caught on Camera BEFORE Explosion!

Security camera video from Nashville, TN shows what appears to be a Directed Energy Weapon coming down out of the sky and burning the AT&T Data Center location just seconds BEFORE a massive explosion erupted.  We have the video!

Before we go farther, you need to understand that the AT&T data center in Nashville, TN, which is where this explosion took place, is an absolutely CRITICAL piece of United States communications infrastructure.   It is a primary hub for VoIP traffic (Voice Over Internet Protocol) and is a primary data collection center used by the United States National Security Agency (NSA) to intercept telephone calls and keep stored copies of those phone calls.

The map below shows how few such centers exist, and the critical location of the Nashville Center relative to the rest of the system:

The damage done to this AT&T facility knocked out 911 Emergency call centers in most of Tennesee, parts of kentuck and even parts of Alabama.   It also knocked out AT&T cellular services in much of Tennessee, knocked out airport Control Tower radio communications with aircraft, and completely cut off most Internet services in much of Tennessee.  Big impact on communications.


The video below aired on local television in Nashville and the news reporter whose voice can be heard, describes what he is seeing as “something coming up off the ground into the sky . . .” as giant flames from an explosion rise up into the air. Here, pay VERY close attention to the first five seconds:



But a closer look at what the reporter describes as “goes up into the sky” reveals that what is seen is a directed energy weapon fired FROM the sky, and whose beam is obstructed by the low level cloud cover as the beam moves with the satellite.

What makes it clear this is an energy beam is that it TRAVELS to the right IN COMPLETE UNIFORMITY at significantly high speed . . . thus proving it is NOT something “coming up from the ground” but rather a beam moving at high speed because a space satellite in orbit, WHICH FIRED THE BEAM,  is moving at such a high speed relative to the ground!

Very shortly after the beam is visible, gigantic flames from a ground explosion rise up from the ground below.

If this was something shooting up from the ground, them it would have a smoke/debris trail which would LINGER, being gently pushed by winds.  But that’s NOT what we see.  We see the “smoke trail” moving at high speed, and very uniformly toward the right . . . which is NOT a characteristic of a smoke/debris trail.


There is NO BLAST CRATER on the ground where the Recreational Vehicle (RV) allegedly exploded.

In countless images from countless other truck bombings, a large blast crater is always clearly visible in the aftermath.  Not in Nashville!   NO BLAST CRATER exists on the public street where this RV exploded.

Here’s a few images, see any crater?

MORE . . .


Debris on the ground outside the AT&T data center shows al long, stainless steel, ELEVATOR PISTON from an underground hydraulic elevator inside the AT&T data center, laying outside on the sidewalk.

In the images below show images of the debris in the top photo, and how the street looked BEFORE the explosion, in the bottom photo.

In the top photo, the steel elevator piston is contained within the red outlined area and the street elevator shaft it came out of is shown in the green outlined area.  Here, look: 

The condo complex where I reside has this exact type of elevator piston.

The piston was installed before the condo complex roof was put on.   It is a long piston that allows an elevator in our building to service the ground level and the three residential levels above it (about 40 feet long.   The piston has to be installed from the roof because it is NOT a telescoping piston; it is one, long, piece of steel, lowered into place by crane during construction.

At the bottom end of the piston is a flexible connection segment, as is clearly visible in the photo from Nashville.

If the explosion that took place was solely from an RV on the street, there is no physical way possible for the underground elevator piston to have been hurled upward toward the explosion from underground.   The explosion HAD to take place inside the AT&T data center in order to hurl that elevator piston upwards out of the ground and on to the street!

Video showing a blast on the street are actually showing the blast which began inside the AT&T data center, finally breaking through the foundation of the building and erupting onto the street, enveloping the RV.

The investigation by law enforcement is ongoing.  But there are serious questions arising about this incident, and there is already empirical physical evidence proving something much bigger took place in this situation than we’re being told.

It seems clear the AT&T data center was the target of this attack.  It seems whoever attacked the data center WANTED to disrupt communications in the US.  They also WANTED to do something to the NSA telephone recording and data collection abilities.

But police report that the RV had a loudspeaker and a recorded message telling people to evacuate.  I know of no bomber who ever did that.   

One possibility is maybe a “deep state” perpetrator needed to do this, but was warned not to cause innocent casualties????? Who ELSE has access to directed energy weapons and would also NEED to destroy evidence in a data collection facility?

Another possibility is that a foreign nation attacked us.  Again.  With the same weaponry repeatedly seen used to start wildfires in California, Oregon and Washington State.


I’m going to reveal something now that will make a lot of people angry.   Inside Nashville AT&T Data Center, Room 641A is the specific data collection point operated by AT&T for the National Security Agency (NSA). It is part of the Warrantless interception perpetrated by government under the PATRIOT ACT.

What part of the United States does this particular room cover? Georgia.

By damaging this data center, it will make it almost impossible to monitor the upcoming Runoff Election for US Senate within the State of Georgia scheduled for January 5.

Whoever did this may have wanted to prevent anyone from repeating the capture of phony voting tabulation which was caught during the November 3 Presidential election.  As most rational people already realize,  that November 3 election was stolen by Democrats to illegitimately claim the Presidency for Joe Biden.  Now they seem to want to steal the US Senate too.

So either the “Deep State” is trying to hide their upcoming theft of the Georgia US Senate runoff election, or perhaps they’re on the run, trying to destroy evidence?  The other possibility is that a foreign power is attacking US infrastructure to hamper communications before they . . . . what . . . . attack?

Either way, this Nashville incident has trouble written all over it, either from a Deep State, false flag or from a foreign power trying to weaken the nation and hamper communications.


Human Activity Is Changing Space? Really?

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There’s a Human-Made Barrier in Space, Surrounding The Entire Earth

15 DECEMBER 2020

In 2017, NASA space probes detected a massive, human-made ‘barrier’ surrounding Earth.

And tests have confirmed that it’s actually having an effect on space weather far beyond our planet’s atmosphere.

That means we’re not just changing Earth so severely, scientists are calling for a whole new geological epoch to be named after us – our activities have been changing space too.

But the good news is that unlike our influence on the planet itself, that humungous bubble we created out in space is actually working in our favour.

Back in 2012, NASA launched two space probes to work in tandem with each other as they whizzed through Earth’s Van Allen Belts at speeds of around 3,200 km/h (2,000 mph).

Our planet is surrounded by two such radiation belts (and a temporary third one) – the inner belt stretches from around 640 to 9,600 km (400 to 6,000 miles) above Earth’s surface, while the outer belt occupies an altitude of roughly 13,500 to 58,000 km (8,400 to 36,000 miles).

In 2017, the Van Allen Probes detected something strange as they monitored the activity of charged particles caught within Earth’s magnetic field – these dangerous solar discharges were being kept at bay by some kind of low frequency barrier.

When researchers investigated, they found that this barrier had been actively pushing the Van Allen Belts away from Earth over the past few decades, and now the lower limits of the radiation streams are actually further away from us than they were in the 1960s.

So what’s changed?

A certain type of transmission, called very low frequency (VLF) radio communications, have become far more common now than in the 60s, and the team at NASA confirmed that they can influence how and where certain particles in space move about.

In other words, thanks to VLF, we now have anthropogenic (or human-made) space weather.

“A number of experiments and observations have figured out that, under the right conditions, radio communications signals in the VLF frequency range can in fact affect the properties of the high-energy radiation environment around the Earth,” said one of the team, Phil Erickson from the MIT Haystack Observatory in Massachusetts, back in 2017.

Most of us won’t have much to do with VLF signals in our everyday life, but they’re a mainstay in many engineering, scientific, and military operations.

With frequencies between 3 and 30 kilohertz, they’re far too weak to carry audio transmissions, but they’re perfect for broadcasting coded messages across long-distances or deep underwater.

One of the most common uses of VLF signals is to communicate with deep-sea submarines, but because their large wavelengths can diffract around large obstacles such as mountain ranges, they’re also used to achieve transmissions across tricky terrain.

It was never the intention for VLF signals to go anywhere other than on Earth, but it turns out they’ve been leaking into the space surrounding our planet, and have lingered long enough to form a giant protective bubble.



When the Van Allen Probes compared the location of the VLF bubble to the bounds of Earth’s radiation belts, they found what initially looked like an interesting coincidence – “The outward extent of the VLF bubble corresponds almost exactly to the inner edge of the Van Allen radiation belts,” said NASA.

But once they realised that VLF signals can actually influence the movement of the charged particles within these radiation belts, they realised that our unintentional human-made barrier has been progressively pushing them back.

One of the team, Dan Baker, from the University of Colorado’s Laboratory for Atmospheric and Space Physics, referred to this as the “impenetrable barrier”.

While our protective VLF bubble is probably the best influence we humans have made on the space surrounding our planet, it’s certainly not the only one – we’ve been making our mark on space since the 19th century, and particularly over the past 50 years, when nuclear explosions were all the rage.

“These explosions created artificial radiation belts near Earth that resulted in major damages to several satellites,” the NASA team explained.

“Other anthropogenic impacts on the space environment include chemical release experiments, high-frequency wave heating of the ionosphere and the interaction of VLF waves with the radiation belts.”

Astronomer Carl Sagan once wanted to find unequivocal indications of life on Earth from up in space – turns out, there are a bunch of them if you know where to look.

The research was published by Science Space Reviews.

A version of this story was first published in May 2017.


Digital Passport Anyone?

Yes, Bill Gates Said That. Here’s the Proof.

Gates and his minions insist the billionaire never said we’d need digital vaccine passports. But in a June 2020 TED Talk, Gates said exactly that. Someone edited out the statement, but CHD tracked down the original.

Some chiseler altered Bill Gates’ June 2020 TED Talk to edit out his revealing prediction that we will all soon need digital vaccine passports (slide 1). But after considerable effort, we tracked down the original video (slide 2).

Gates’ minions on cable and network news, his public broadcasting, social media and fact-checker toadies all now insist that Gates never said such things. They say he never intended to track and trace us with subdermal chips or injected tattoos.

They dismiss such talk as “conspiracy theories.”

Well, here it is from the horse’s mouth.

In 2019, according to a not-yet-purged Scientific American article, Gates commissioned the Massachusetts Institute of Technology to build an injectable quantum dot dye system to tattoo stored medical info beneath children’s skin. The tattoo was designed to be readable by an iPhone app.

Gates’ company, Microsoft, has patented a sinister technology that uses implanted chips with sensors that will monitor body and brain activity. It promises to reward compliant humans with crypto currency payments when they perform assigned activities.

Gates also invested approximately $20 million in MicroCHIPS, a company that makes chip-based devices, including birth-control implant chips with wireless on/off switches for remote-controlled drug-delivery by medical authorities.

In July 2019, months before the COVID pandemic, Gates bought 3.7M shares of Serco, a military contractor with U.S. and UK government contracts to track and trace pandemic infections and vaccine compliance.

To facilitate our transition to his surveillance society, Gates invested $1 billion in EarthNow, which promises to blanket the globe in 5G video surveillance satellites. EarthNow will launch 500 satellites allowing governments and large enterprises to live-stream monitor almost every “corner” of the Earth, providing instantaneous video feedback with one-second delay.

The Bill and Melinda Gates Foundation also acquired 5.3 million shares of Crown Castle, which owns 5G spy antennas including more than 40,000 cell towers and 65,000 small cells.

Please make your own copy of these clips — as Gates’ power to disappear inconvenient facts is expanding every digital day.


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.


Some Real Expert Opinions

Take a few minutes to listen to what unbiased physicians and health professionals who are not in the pay of Big Pharma have to say:

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.


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.