The U.S. Food and Drug Administration (FDA) is likely to grant Emergency Use Authorization (EUA) for Pfizer’s BioNTech SARS-CoV-2 vaccine for children ages 6 months through 4 years and Moderna’s COVID-19 mRNA vaccine for infants and children ages 6 months through 5 years and 6 years through 17 years in their upcoming meetings today and tomorrow (June 14-15).
CHD is poised to take legal action against the FDA should they grant these emergency use authorizations. We seek to hold FDA accountable for recklessly endangering our children with products that have little, no or even negative net efficacy. These products may put them, without warning, at risk of many adverse health consequences, including heart damage, stroke, other thrombotic events and future reproductive harm.
Our children need your help! On Tuesday and Wednesday, June 14 and 15, the FDA VRBPAC committee is likely to make a catastrophic decision by voting to grant Emergency Use Authorizations (EUA) to allow for infants and young children to receive Pfizer’s and Moderna’s COVID shots.
Please take 30 seconds to tell your lawmakers to STOP the FDA from granting EUAs for COVID vaccines in babies and children by sending Robert F. Kennedy, Jr.’s letter to FDA VRBPAC committee members. His letter lays out all of the available science and data that proves vaccinating children for COVID is not only unnecessary, but will recklessly endanger their lives. There is no emergency whatsoever for children from COVID, therefore there is no justification for issuing an Emergency Use Authorization.
Time and mounting evidence have continued to prove that children have essentially zero risk of dying from COVID (99.995% recovery rate), and the vast majority of kids have little to no symptoms. There is no statistically valid evidence that shows the Pfizer and Moderna COVID injections are able to prevent severe disease or deaths in children at all. These shots have a worse safety record than all previous vaccines combined, and have been found to cause serious injuries including myocarditis, encephalopathy, blood clots, diabetes, neurological issues and death.
The United States Government, at the behest of Pharma oligarchs and government employees who own stock in the Pharma companies, hopes to approve an amendment to the EUA (Emergency Use Authorization) to inject babies 6-months-old to toddlers 4-years-old with the C19 faux-vaccine.
Before the committee meets to recommend the amendment, the FDA allows people to comment on the FDA government web site. One such comment was provided to this author and is offered to you below. The United States of America is indeed facing a government #ClotShot plot.
This comment is NOTICE of possible criminal liability to Lauren K. Roth and members of the Vaccines and Related Biological Products Advisory Committee who owe duties of care, diligence, good faith, and loyalty in recommending “for” or “against” the EUA amendment for COVID-19 mRNA vaccine in children 6 months through 4 years of age.
Only two deaths are listed herein to establish knowledge. If the amendment is approved, it will have been done by committee members “knowing” of felony crimes in context.
Your investigation of these deaths should include death certificates, autopsy records, witness interviews, and immunization records.
Massachusetts Death Certificate 2022 SFN 5980 is a 7yo girl died January 18, 2022 listed as died from U071 “COVID-19”, B49 “unspecified mycosis”, J450 “predominantly allergic asthma”, and R091 “pleurisy”.
VAERS_ID 2038120 is a 7yo girl in Massachusetts, who received her 2nd dose 1/13/2022 and was reported to VAERS 1/15/2022. PRIOR_VAX states, “Severe nausea and vomiting from 5min post vaccination and for the next 8-10 hours.” SYMPTOM_TEXT states, “Spiked a 103 fever, severe stomachache, has not had a bowel movement since the day before vaccination, which makes today 3 days without one. First vaccine caused severe nausea and vomiting from 5minutes post injection and for the next 8-10 hours.”
This little girl suffered immeasurably 4 to 5 days as her intestines shut down due likely to impeded blood vessels servicing intestines.
Massachusetts Death Certificate 2021 SFN 56611 is a 48yo man died 11/16/2021 listed as died from U071 “COVID-19” and E669 “OBESITY”.
SFN 56611 is known to have died less than 24 hours after inoculation.
In both cases, the Medical Examiners listed the cause of death as “COVID-19”, when it was clearly not COVID-19. And in both cases, the Medical Examiners omitted listing causes Y590 “Viral vaccines“ and T881 “Other complications following immunization, not elsewhere classified”, when these clearly were proximate and actual causes.
Death certificates from the state of Massachusetts are sent to the CDC, a federal entity. Thus, fraud on a state death certificate is a federal crime as it affects federal death records. Several federal felony crimes apply in this instance and are listed below.
If you dismiss this NOTICE and recommend the EUA amendment without first investigating these two deaths, you become liable for inchoate crimes and the felony crime of “misprision of felony.” If a single person subsequently dies as a result of the amendment, all the elements will have been satisfied for you to face felony murder charges or involuntary manslaughter. Qualified immunity is not a valid defense.
18 USC § 4 – Misprision of felony
“Whoever, having knowledge of the actual commission of a felony …, conceals and does not as soon as possible make known the same to some … civil or military authority …, shall be fined under this title or imprisoned not more than three years, or both.”
Felony murder is a homicide that occurs during the commission of an inherently dangerous felony, showing a conscious disregard for human life. A jury decides whether recommending an injection, that you “know” caused death, and that you refused to investigate while “knowing” it caused death, is inherently dangerous.
Here are a few federal statutes likely violated by Medical Examiners in Massachusetts. You are duty-bound to call for investigation of:
18 USC § 4 Misprision of felony
18 USC § 286 Conspiracy to defraud the government with respect to claims
18 USC § 287 False fictitious or fraudulent claims
18 USC § 371 Conspiracy to commit offense or to defraud United States
18 USC § 1035 False statements relating to health care matters
18 USC § 1040 Fraud in connection with major disaster or emergency benefits
There were found sixty likely C19 vaccine deaths in a 25-minute perusal of the 2021 and 2022 death certificates, which extrapolates to hundreds, probably thousands of C19 vaccine deaths in Massachusetts.
Refusal to investigate these fraudulent records is a crime that, because of the felony murder aspect, has no statute of limitations. Five, ten, or twenty years from now, if a federal prosecutor were to learn of this NOTICE, he or she would have significant evidence to bring charges for felony murder.
In summary, this NOTICE places you in a position requiring you to investigate these deaths prior to recommending the amendment. If you dismiss this NOTICE, you may be criminally liable for involuntary manslaughter, felony murder, and a list of federal crimes and inchoate crimes.
Please make the appropriate decision for yourselves and for the children of the United States of America.
A growing number of young healthy adults are mysteriously dying. Watch Jefferey Jaxen and Del try to make sense of, what is now being called, “Sudden Adult Death Syndrome” (SADS).
First New England Journal of Medicine Pfizer Study Reveals 80% Miscarriage Rate in Recipients in their First or Second Trimester — Dr. Christiane Northrup also reports rising number of stillbirths on ‘Friday Roundtable’ Infertility: A Diabolical Agenda Q+A
Americans across the country have been faced with discrimination. We have received many questions as to the correct process to rectify this. Our legal team has put together a step-by-step guide to help you through the process. If you have been discriminated against please see the instructions below. Everyone can start taking action now if they have faced discrimination in the workplace.
Our legal team has broken it down into 3 steps:
STEP 1: FILE A COMPLAINT WITH THE EEOC.
STEP 2: FILE A COMPLAINT WITH YOUR STATE GOVERNMENT.
STEP 3: FILE A CIVIL LAWSUIT.
For full detailed information on the steps for each state, please see the guide below.
The object of war is to kill or maim as many people as possible, by whatever means. However, outright killing is often less efficient than wounding because more of the enemy’s resources are consumed in caring for the wounded than burying dead bodies. The overall goal of war is to conquer and subdue a people. In the process of conquering, the enemy must be psychologically and physically broken to the point that they give up their will to fight and their will to assert self-determination.
The current pandemic war has all the markings of more traditional militaristic war except that it is still unrecognized by those who are under attack. It is the perfect stealth war. History is full of examples of stealth attacks that were extremely successful. The victims never saw the attackers until it was too late to resist.
In today’s war, the entire health system has been weaponized and turned into a giant Trojan horse. Obey, obey, obey it cries. Humiliate yourself by donning a face mask, by staying home and retreating from normal society. Mutilate yourself by giving up your job, closing your business, injecting harmful substances into your body.
Meanwhile, dead bodies are piling up in record numbers. It’s an old-fashioned genocide with a medical twist.
For a minute, forget case numbers, hospital beds and epidemiological studies. The Expose provides a back-door look at what’s going on by analyzing ambulance call-outs, all of which are nicely recorded and detailed:
The National Health Service has confirmed in response to a freedom of information request that ambulance call-outs relating to immediate care required for a debilitating condition affecting the heart nearly doubled in the whole of 2021 and are still on the rise further in 2022. But the most concerning published figures show that they have also doubled among people under the age of 30.
What group is getting hit hardest? Young people under 30 – those normally suited for military service, i.e., to build a physical army. Overall, emergency calls for heart-related incidents has skyrocketed from the first day of Emergency Use Authorization injections.
The tidal wave of propaganda – just like in any war – is designed to deceive, demoralize and confuse. Prominent medical journals spit out headlines like:
They all state that your eyes are lying to you. Rather, you should trust the propaganda that sows just enough doubt that you don’t dare open your mouth in public about such silly things as ambulance call-outs for heart-related emergencies.
This writer has continuously stated since December 18, 2015 that Technocracy declared war on the entire human population of the world. I wrote, “Technocracy is the same nefarious ideology that enabled Adolph Hitler in the 1930s. Nazi Germany used advanced technology to enslave and kill millions of its own citizens. This hasn’t happened here yet, but this is the direction we are headed.”
We have arrived.
What level of stupidity and ignorance do people have to exhibit to not see what is going on here?
The U.S. Food and Drug Administration (FDA) is declaring war on our children and it’s on each of us to be unrelenting as we defend the next generation from Big Pharma and its allies. We must stop the FDA’s attack, beginning with a campaign to end unethical and unsubstantiated Emergency Use Authorizations (EUA) that will subject our younger and most vulnerable children to the unnecessary risks of COVID shots.
The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) is scheduled to meet on four separate occasions in June to discuss additional EUAs that would provide cradle-to-grave COVID shots and consider a “Future Framework” that will permanently lower the bar for safety and efficacy going forward.
Their itinerary is as follows:
June 7 — Emergency Use Authorization for Novavax’s COVID shot for adults.
June 14 — Amendment to Moderna EUA to include primary series to children and adolescents 6 through 17 years of age.
June 15 — Amendment to Moderna’s EUA to include primary series for children 6 months to 5 years and amendment to Pfizer’s EUA to include the primary series to children 6 months through 4 years of age.
June 28 — Proposed “Future Framework” for COVID shots.
Dr. Toby Rogersaptly calls the June meetings a “blitzkrieg” because it is an overwhelming all-out attack (on informed consent) designed to create psychological shock and demoralizing chaos. But we can change the outcome by arming up with real data and creating a blitzkrieg of our own.
We need Defenders like YOU to hold the line and stop the approval of EUA amendments that profoundly impact the health and safety of our kids. Tell VRBPAC members that:
There is no COVID emergency for children.
Children under 18 with no comorbidities have virtually no risk of death from COVID. They have a 99.995% recovery rate and the vast majority of children have minimal symptoms. A study published in Nature described how children between 3 and 11 years of age mount effective, robust and sustained immune responses to COVID. The CDC’s own data show that at least 75.2% of children ages 0 to 11 years and 74.2% of adolescents ages 12 to 17 years already have superior natural immunity.
mRNA shots offer little in the way of protection.
There is no clinically significant health benefit from the mRNA vaccines. Moderna’s own press release acknowledges that “the absence of any severe disease, hospitalization or death in the study precludes the assessment of vaccine efficacy against these endpoints.” Preliminary data showed the shots were only about 44% effective at preventing symptomatic infection in children 6 months to 2 years old, and 37% effective in children ages 2 to 5 years old — both below the 50% level that regulators had generally called the minimum level for EUA approval in 2020. In New York, officials observed that Pfizer’s efficacy against Omicron plummeted from 68% to 12% after 7 weeks in children ages 5 to 11.
Injuries from COVID shots in children are catastrophic.
Vaccinated children face a substantial risk of myocarditis. Moderna’s EUA application, originally filed in June 2021, has already been held up because of a clear safety signal for myocarditis, which has prompted a number of European countries to prohibit its use in young people. Additionally, the Vaccine Adverse Events Reporting System (VAERS) has over 48,500 reports of adverse events in children, including 112 deaths (as of May 20, 2022) and a growing number of reports of encephalopathies, clotting issues, diabetes and neurological issues in children following COVID shots.
The FDA is poised to make decisions regarding our children and the future of this country that may have a devastating impact on children’s health.
Please send a message to FDA and CDC officials, VRBPAC members and elected representatives demanding that they reject the Pfizer and Moderna EUA applications for children and ensure our government agencies are following the science.
The doctors, scientists and journalists featured in THE VIRAL DELUSION examine in detail the scientific papers that were used to justify the pandemic, and what they find is shattering. In this shocking, five-part, seven hour documentary series, they explode every single major claim, from the “isolation” of the virus to its so-called genetic sequencing, from the discovery of how to “test” for SARS-CoV2 to the emergence of “variants” that in reality, they explain, exist only on a computer. Their point: that the so-called SARS-CoV2 virus exists only as a mental construct whose existence in the real world has been disproven by the science itself.
They then go back through history to reveal how the birth and growth of virology has led to massive misunderstanding and misdiagnosis of disease: from Smallpox to the Spanish Flu, Polio to AIDS, to COVID itself – putting the pandemic in a whole new context better understood not as settled science, but the tragic culmination of misunderstood biology by the growing cult of virology, built on pseudo-science, to which much of the rest of the medical profession defers without understanding or examination, and the tragic consequences that have been wrought in its name.
In 2019, the virologists took center stage, and for the first time on film, their methods, miscues and tragedy they have wrought are put under the spotlight, revealing the extraordinary leaps of fantasy buried in their methodology, the contradictions quietly acknowledged in their papers, their desperate effort to change language to justify their findings, the obvious incongruence of their conclusions and the extraordinary stakes for our entire society in whether we continue to blindly follow their lead into a full-scale war against nature itself.
Featuring: Andrew Kaufman, MD; Tom Cowan, MD; Stefan Lanka, Virologist; Torsten Engelbrecht, journalist; Claus Kohnlein, MD; Kevin Corbett, PhD RN; David Rasnick, Biochemist PhD; Mark Bailey, MD; Dawn Lester and David Parker, Authors; Stefano Scoglio, Biochemist PhD; Saeed Qureeshi, Chemist PhD; Celia Farber, Journalist; Harold Wallach, PhD; Pam Popper, PhD, ND; Charles Geshekter, PhD; Amandha Vollmer ND, Jim West, Author; Larry Palevsky MD; and more.
The Viral Delusion (2022) Episode 1:The Tragic Pseudoscience of SARS-CoV-2
When doctor Andrew Kaufman began reading the first virology papers out of Wuhan in December 2019, he was shocked to discover that the scientists had come nowhere close to proving that a new virus had emerged… yet saw the media and authorities already claiming a viral pandemic was on it’s way.
In this extraordinarily revealing opening episode, a group of biologists, chemists, doctors and journalists take apart the SARS-COV-2 narrative piece by piece — from the non-isolation of the virus, to the hidden problems with purported photographs of the virus, to the claims that it has been genetically sequenced, to the invalidity of the PCR “covid-test.”
From the treatment protocols for COVID to the assumption of its transmission, Episode One unpacks the science of the claims that changed the world – in which these doctors and scientists make the case that every single claim the authorities made about the so-called SARS-COV2 virus has been based not on evidence, but pseudoscience.
The Viral Delusion (2022) Episode 2: Monkey Business: Polio, Measles And How It All Began
How did it all begin?
How could the scientific establishment have possibly gotten so big a story so wrong?
Everyone knows the story of Polio…or do they?
What from that story is actual history and what is medical marketing?
How did a small branch of the scientific establishment come to convince the world polio was the result of a virus and not from environmental toxins?
Learn what the actual experiments were upon which this theory was based — and how shockingly unconvincing they are.
Discover too how the medical establishment’s efforts to squeeze the symptoms of polio into a virus model formed the very foundation of modern virology, and how that commercially successful model has steered modern science ever since, evidence be damned.
The Viral Delusion (2022) Episode 3: The Mask of Death – The Plague, Smallpox and The Spanish Flu
What about Smallpox?
The Spanish Flu?
The Black Plague?
Go back, back, back in time to examine the claims and counter-claims as to what truly caused these deadly epidemics.
Are the rats of Europe innocent? Turns out they have to be…
And in that discovery we see how the superstitions of our time have clouded the eyes of “science” to avoid the most obvious of insights about disease.
The Viral Delusion (2022) Episode 4: AIDS, The Deadly Deception
AIDS. It was the defining epidemic of a generation.
But it was also the coming of age for many leading scientists and doctors who came to realize that blaming the illnesses known as AIDS on a virus was not only unsupported by science, it was downright nonsensical.
What were the true causes of the many illnesses labelled AIDS around the world?
How many suffered from their misdiagnosis?
How the scientific establishment fell into the deadly AIDS delusion is crucial to understanding the pandemic, and health, today.
The Viral Delusion (2022) Episode 5: Sequencing The Virus, Without The Virus
With the rise of computing and genetic research in the 90’s the virologists go high-tech.
They move away from experiments altogether and into genetic modeling — but do the models have any connection to reality?
The wonders of genetic sequencing have been pointed to as the proof of virology’s explanatory power — but when the claimed sequencing of SARS-COV2 is put under the microscope, has the game changed from the realm of science, to science fiction?
What’s really going on the claim of genetically identifying the SARS-CoV-2 virus is made?
The picture above is of a sign outside a performing arts theater in Santa Barbara, California. Looks like everyone is welcome. Well, not really. It turns out that if you’re not “vaccinated” you’re not welcome. If you haven’t arrived at the ticket booth with ID and proof of being injected with two doses of an emergency use experimental gene treatment for “covid 19” — a treatment which has no efficacy and is associated with millions of serious injuries and deaths — this #LoveForAll message doesn’t actually apply to you. If you’re not “vaccinated” the only way you can get into the theater now is if you have taken a test proving you don’t have the plague. Don’t want a PCR swab up your nose? Too late for an antigen test? Tough luck. This rainbow venue welcomes EVERYONE, except for carriers of the plague.
“Who doesn’t love LOVE?” Apparently, the state of North Carolina doesn’t. The founder of Insist On Love For All which makes and sells the $60 sign displayed above, took a trip to Asheville, North Carolina a few years ago and was impressed by signs “embracing diversity.” Says Insist On Love’s founder,
shop owners started displaying these signs over two years ago [2018] to encourage tourism following the passage of the controversial House Bill 2 in North Carolina, which requires certain public bathrooms to be designated for use by males or females based on their biological sex. “The signs in Asheville moved me. Love is the only weapon we can use to fight hate . . . “
In this case, “hate” was displayed by 1) the idea that men and women should have separate bathrooms, 2) the idea that men (or men who think they’re women) don’t have a right to walk into women’s bathrooms, and vice versa, 3) the fact that other sexes besides male and female have not been acknowledged, and 4) the fact that the state of North Carolina thus discriminated against all those who don’t have male/female privilege. There is also the ‘hate’ involved in the unwillingness of North Carolina to provide separate bathrooms for a theoretically unlimited number of other genders. Unless #LoveForAll is somehow a front for a consortium of plumbing supply companies (this would actually be comforting news), there is nothing left for us to conclude but that ‘love’, as the term is being used here, is indeed a weapon, not to fight hate, but to fight reason. ‘Love’ is now a buzzword in a well-established “diversity and inclusion” narrative sent down from academic critical theory to the progressive left to the mainstream media to the culture at large. Has there ever been a time when good things have been so twisted into their opposite? This is not about love or inclusion. This is shallow virtue signaling by people who have been swallowed up by a political machine designed to turn cultural norms upside down, not for the purpose of bringing needed change, but for the purpose of creating chaos and a loss of rationality, after which new supposed norms can just be lifted into place.
“All sexual orientations”, cited in the sign, is also a topic at the current May 22-28 Davos forum, where “resilience through equity” and “inclusivity” for the “LGBTQI+ community” is on the formal agenda. Do the corporate bosses, social engineers, and preening politicians at this forum really care about equality, or are they just using the brand to create the upheaval necessary to bring in fantastic profits and power? The answer is obvious. The agenda is exclusion, not inclusion; fascism, not liberalism. Their plan is for the majority of humanity, gay or straight, to be excluded from their rights, autonomy, and independence, while the bosses enjoy their wealth and slave labor. Like #LoveForAll, everyone is welcome in the Great Reset except those who believe there are only two sexes — that is, just about everybody since the beginning of human history. Everyone is welcome in virtue-signaling countries, corporations, and institutions except those who choose not to accept a medical intervention also never heard of before in human history — that of altering the human genome on the pretext of defeating a virus. In other words, everyone is welcome except those who have chosen not to go insane. The insanity is called wokeness. Wokeness is nothing but a tool being used to effect a very ugly and very ambitious power grab. When the job is done, everyone duped into thinking they were fighting for the victims of oppression and equality for all will be swatted away like flies.
The would-be gods at Davos brought us their own version of the Apocalypse — plague, war, famine, and death became covid, Ukraine, food shortages, and vaccines. Do such people even remotely care about racial prejudice and gender dysphoria? No. They either massively exploited or completely made up these issues to create disorder. Indeed, their eugenicist predecessors had certain, ahem, opinions about people with disabilities, sexual deviants, and racial groups which they know can’t be mentioned in polite society today. So they went the other way. Not believing in God, the Davos elite see themselves as gods. The further this delusion takes them, the harder they will fall. There will also come a time of reckoning for the collaborators in this program — those who, wittingly or not, aided this monstrosity. Galling self-righteousness, ignorance, and hypocrisy were the least of the crimes in this class. The ones higher up — those who made the plans, gave the orders, and knew what they were doing — face a reckoning that perhaps we do not have words for. It may be a regular new round of guillotining such as we have seen before in history. Or it may be that this time wickedness has gone so far it will have to be ended forever. Prospects for the Davos crew do not look good.
Richard Hugus is the founder of Cape Cod Against Medical Mandates. “We are residents of Cape Cod, Massachusetts who support freedom of choice in all matters having to do with our own and our childrens’ health.” Connect with them here.
Monkeypox – it’s the hip new disease sweeping the globe. Allegedly appearing almost simultaneously in over a dozen different countries on four different continents.
As we wrote in the early days of the Covid “pandemic”, the only thing spreading faster than the disease is fear.
The media reported the first UK case of monkeypox on the 7th of May. Less than two weeks later, we’re seeing some very familiar headlines. Just like that…Pandemic 2: Monkey Pox!! begins playing at all your favorite fear porn outlets.
The BBC went real subtle with it, blaring: “Monkeypox: Doctors concerned over impact on sexual health”
The New Scientist has actually used the P-word, asking “Can Monkeypox become a new pandemic?”, before answering, essentially, “probably no, but also maybe yes!”. Keeping their options open.
Sciencewarns that“Monkeypox outbreak questions intensify as cases soar”
The Mirror has gone full paranoid already, headlining:
Russia looked into using monkeypox as biological weapon, claims ex soviet scientist
So that’s one direction the story might go.
To be clear, “monkeypox” (whatever that even means in this context), is NOT a Russian bio-weapon. It’s not a Western bio-weapon either. Or Chinese bio-weapon. It’s just another scare story. And a rushed, half-hearted one at that.
One of the signs that marked the Covid “pandemic” as a psy-op from an early stage was the sheer speed with which the hysteria spread. Far from learning from their mistakes, the powers-that-be have decided to go even faster this time.
Despite “cases” numbering barely in the dozens, the World Health Organization has called an emergency meeting, a strange thing to do when their annual Assembly starts literally tomorrow. But I guess when your launching a new product you need to do everything you can to get the hype going.
Despite just two “cases” in the entire United States (and indeed the fact they still don’t work), New York is bringing back mask recommendations.
Nobody has said “lockdown”…yet. But Hans Kluge, WHO regional director for Europe, is “concerned” that transmission could accelerate if people attend mass gatherings:
as we enter the summer season … with mass gatherings, festivals and parties, I am concerned that transmission could accelerate”.
(As inflation soars and the cost of living crisis only gets worse, it’s probably handy for them to have a new “public health” reason to ban protests or clampdown on civil unrest. Just a thought.)
There’s some good news though…for vaccine manufacturers, anyway. As Whitney Webb reports, two struggling pharmaceutical companies have already seen a big stock boost from the “outbreak”:
Regardless of how the monkeypox situation plays out, two companies are already cashing in. As concern over monkeypox has risen, so too have the shares of Emergent Biosolutions and SIGA Technologies. Both companies essentially have monopolies in the US market, and other markets as well, on smallpox vaccines and treatments. Their main smallpox-focused products are, conveniently, also used to protect against or treat monkeypox as well. As a result, the shares of Emergent Biosolutions climbed 12% on Thursday, while those of SIGA soared 17.1%.
Just as with Covid, and despite rumours they would be leaving the World Health Organization, Russia appears to be lining up with the WHO agenda. Already they are “tightening border quarantine” rules, vaccinating healthcare workers and supplying quick bedside tests internationally.
Looks like we might be in for an epic summer of scare-mongering, panic-buying & bucketloads of cringe.
Are the new jabs already prepped & ready to go?
Are the “our hospitals are overwhelmed videos” being filmed as we speak, complete with “monkey pox” moulage and crying nurses who turn out to have IMDB pages & multiple acting credits?
Are the sleepy masses going to be fooled yet again?
Children’s Health Defense seeks help from parents in 13 Texas counties, after a U.S. District Court on Tuesday granted CHD 45 days to amend its lawsuit against the U.S. Food and Drug Administration’s Emergency Use Authorization of COVID-19 vaccines for children ages 5 to 11.
A U.S. District Court on Tuesday gave Children’s Health Defense (CHD) 45 days to amend its lawsuit against the U.S. Food and Drug Administration’s (FDA) Emergency Use Authorization (EUA) of COVID-19 vaccines for children ages 5 to 11.
CHD’s lawsuit, filed Jan. 24 in the U.S. District Court for the Western District of Texas, alleges, among other things, that the FDA — under pretext of EUA powers — “authorized a dangerous drug for minor children as young as 5 years old to address COVID-19, which poses less risk to a 5-year-old than the ordinary flu.”
CHD last month filed a motion to stay asking the court to suspend the FDA’s authorization of the vaccine for young children pending judicial review of the lawsuit.
During Tuesday’s hearing Judge Alan Albright heard arguments on CHD’s motion to stay and also on the FDA’s motion to dismiss CHD’s lawsuit.
Judge Alan Albright denied CHD’s request to suspend authorization of the vaccines until the lawsuit is resolved, stating he was skeptical of CHD’s organizational standing and the standing of the two parents named in the suit, given the lack of any children’s COVID-19 vaccine mandate in the district at this time.
Judge Albright said for CHD to have standing, it must show “diversion of resources.”
For the parents named in the complaint — Deborah L. Else and Sacha Dietrich — to have standing, they must show their children are at demonstrable risk of vaccination against the parents’ wishes.
Attorney Robert Barnes, arguing for CHD, said if the FDA’s interpretation of standing were correct, then no one could sue the FDA because it would mean the FDA is completely insulated from judicial scrutiny.
Barnes also argued the harm to plaintiffs is not simply the threat of vaccination, but includes the FDA’s false assertions that the vaccines are safe, effective and actually vaccines, i.e. products that prevent infection and transmission.
U.S. Department of Justice attorney James Harlow, arguing on behalf of the FDA, said the agency cannot mandate products and that products authorized for emergency use clearly permit patients to accept or reject them.
Harlow also argued that Texas Gov. Greg Abbott issued an executive order prohibiting COVID-19 mandates at schools, thus undermining an argument for any threat.
After hearing arguments from both sides, Judge Albright said given the importance of the case, he wanted to give CHD and plaintiffs Else and Dietrich the opportunity to assert standing, and would give them 45 days to amend their lawsuit.
The judge also provided a roadmap for how to amend the case.
CHD is seeking help from the public in order to provide the court the necessary evidence to prove standing in its case against the FDA.
Parents in 13 counties in the Western District of Texas who have information about coercive COVID-19 vaccine policies for children or adolescents are asked to submit that information to chd@childrenshealthdefense.org with subject line “CHD v. FDA.”
The 13 counties are: Bell, Bosque, Coryell, Falls, Freestone, Hamilton, Hill, Leon, Limestone, McLennan, Milam, Robertson and Somervell.
CHD is especially interested in these types of situations occurring in the counties listed above:
Hospitals or medical facilities that require COVID-19 vaccination for treatment
Children in foster care, correctional settings or other institutional settings who are required to receive COVID-19 vaccinations
Vaccination clinics or vaccination stations in schools or youth facilities promoting COVID-19 vaccines for kids
Evidence of school pressure to vaccinate children even without an explicit mandate
After-school programs or extra-curricular activities requiring COVID-19 vaccines.
CHD in May 2021 filed a citizen petition with the FDA and the U.S. Department of Health and Human Services outlining the arguments against EUA and/or licensing of COVID-19 vaccines.
The FDA on Tuesday granted Pfizer’s request for EUA of a third COVID-19 shot for children ages 5 to 11, and the Centers for Disease Control and Prevention on Thursday signed off on the shots.
Have you heard of the World Economic Forum? It’s a secret club where the world’s wealthiest oligarchs meet with globalist politicians to develop schemes to tell the rest of us how to live.
People like Bill Gates. Xi Jinping. Justin Trudeau. And Anthony Fauci.
The WEF’s founder, Klaus Schwab, resembles a cartoonish supervillain from a James Bond movie.
But he’s real. And he has big plans for you. Including the ominous slogan, “you’ll own nothing, and you’ll be happy”.
That’s why I flew all the way to Switzerland, along with a team of investigative journalists, to report on just what these billionaires are up to.
My friend Rukshan Fernando came with me from Australia, and we arrived a couple of days early to get over the jet-lag. And I’m so glad we did. Because wandering through the streets of Davos in the days before the big WEF conference was like going onto a Hollywood movie set before they turn on the cameras.
You can see just how fake everything is. They’re literally putting false storefronts over every building in town.
No expense is spared by these jet-setters, the people who tell you to eat less meat and drive your car less.
And you can see how paranoid they are: hundreds and hundreds of armed men whose job is to stop mere citizens from seeing or hearing things they’re not supposed to.
That’s the craziest part. Swiss police are swarming into the town. But not just police: convoys of military trucks bringing in hundreds of heavily-armed soldiers.
What on earth are they planning to do?
But what’s more alarming to me is seeing so many news and social media companies fully-embedded in the WEF. They are part of it — they’re in on it.
YouTube. The Wall Street Journal. Google. Dow Jones. They have giant kiosks set up at Davos.
They’re not here to report. They’re here to participate. They spent millions to be part of this carnival of the billionaires — they want to get rich off it. And they’re willing to propagate the WEF message, pretending they’re objective news reporters.
That’s why I’m here with the rest of the Rebel News team. We’ll be here all week, and we’ll also visit the World Health Organization’s meeting happening just a few hours away in Geneva. That’s just as worrying — and I’ll tell you why in another report.
But for now, please just make sure you’re going to www.WEFReports.com every day. That’s where the rest of our team and I will be publishing all of our videos from our journey.
And if you think our work as independent journalists is essential — if you think someone needs to be there to tell the other side of the story — please consider chipping in to help our economy-class travel to Davos.
World Wide Rally for Freedom movement stands for human freedoms and sovereignty as the corporate-sponsored WHO moves to take charge of every nation’s health policy
CITIES AROUND THE GLOBE MAY 21 / 22 — On the weekend of May 21-22, 2022, people organizing with World Wide Demonstration, a grassroots international freedom movement, hold their eighth weekend of global rallies to support fundamental human rights and sovereignty even as the World Health Organization (WHO) begins their World Health Assembly meeting May 22 in Geneva, Switzerland to amend the International HealthRegulations of 2005 (IHR) and continue negotiations for a new global Pandemic Treaty. The proposed amendments and treaty hearings to-date indicate thecorporate-sponsoredWHOisusing these maneuvers to attempt to gain powers that supersede rightsprotected by national constitutions. By amending existing health regulations, the WHO believes they will be able to bypass the need for direct approval from national government bodies and to avoid public debate or media coverage.
WWD stands for the sovereign right of humans to make their own individual health decisions, free from any corporate or governmental coercion or threats, affirming hard-won human rights accords.
Currently 80% of WHO funding comes from privatecorporations, including pharmaceutical companies, which demonstrates the glaring conflicts of interest the WHO has in devising health recommendations. We recognize their move to amend the IHR and push a new treaty as a straightforward corporate power grab under the guise of “health.” When corporations can use proxy organizations to order everyone in the world to take a product they make, the billions raked in create a powerful incentive to conjure the next crisis. It’s approaching common knowledge that the WHO’s draconian recommendations over the past two years were put in place not to improve human health, but to create windfall Pharma profits, to fuel fears, and to groom the population to accept tyrannical control levers over each person’s individual decisions that can be wielded by a few unelected billionaires.
World Wide Rally for Freedom events will take place in many cities in many countries all over the world. Check the official WWD telegram channel for an updated list.
One Day. Everyone Together. We Will All Be There.
We stand for 5 important Freedoms:
Freedom of Speech.
Freedom of Movement
Freedom of Choice.
Freedom of Assembly.
Freedom of Health.
Many of our 5 important Objectives are being realized one by one. We continue to rally to ensure these damaging infringements of rights are ended foralltime:
End Lockdowns
End Mask Mandates
Prevent Vaccine Mandates and Coercion
Return to Standard International and Domestic Travel
End all State of Emergency Declarations
We have built our Movement upon 5 important Principles:
Decentralization
Collaboration
Community
Stability
Peace
We advocate for 5 Solutions:
Non-Compliance
Empowerment
Freedom Preserving Institutions
Freedom Culture
Shift The Narrative
We will not allow our inalienable Human Rights to be re-packaged as Human Privileges, to be conditioned upon compliance with authoritarianism.
Throughout history, humanity has been tried and tested in difficult times, but in the end, freedom always wins.
We can overcome any fears by building new social relationships and new systems that do function in respect of human rights.
###
World Wide Demonstration: In the spring of 2020, the idea of a world wide demonstration to stand up for our human freedoms in the face of never-ending lockdowns was born. The idea spread virally — the idea resonated around the world — and resulted in millions of everyday people taking to the street in peaceful rallies in hundreds of cities beginning March 2021. We believe that fundamental rights are not privileges, and we stand for peace, freedom, democracy and solidarity. We are mothers and fathers, children and grandchildren, grandmothers and grandfathers, brothers and sisters, young and old. We are the People. We are the Society.
“I would love to be able to bring back our country into a great form of unity,” Trump said. “Without a major event where people pull together, that’s hard to do. But I would like to do it without that major event because usually that major event is not a good thing.” – Donald Trump, Jan 30th 2018
By April of 2020, within two years of Donald Trump’s prophetic message, millions of people had bowed the government’s request to “unite” by “social distancing,” under a “Live Exercise” revealed by Trump’s Secretary of State Mike Pompeo. About half of the world’s population agreed to some form of lockdown. More than 3.9 billion people in more than 90 countries had been asked or ordered to stay at home by their governments. And they did.
In unison, millions donned a ritual mask to protect themselves against an invisible enemy. The effect was dubbed virtue signaling – an attempt to show other people that you are a good person, by expressing opinions that will be acceptable to them, especially on social media. How did so many people fall into lock-step to give up their freedom when they had previously been openly skeptical of government ethics and policies?
Social Engineering
The earliest social experiments had been successful using the tried-and true strategy of The Hegelian Dialectic: Problem • Reaction • Solution. Introduce a Problem and roll out the Solution! Past experiments included “The New Deal” under Franklin Roosevelt in the 1930s, and “Great Society” under Lyndon Johnson in the 1960s. Then came the “financially sound” government programs of Social Security, Medicare, and Medicaid.
Money and politics aside, why trust a government’s blanket medical solution when it comes to health, a personal responsibility?
If we understand the mechanism and motives of the group mind, it is now possible to control and regiment the masses according to our will without them knowing it. – Edward Bernays
After three years of government-induced COVID, there is still no approved government Solution to the COVID Problem because the FDA-approved vaccine is still not officially available to anyone, and may never be. Nonetheless, the Live Exercise of testing, tracking, experimentation, and restrictions, continues unabated.
While vaccine makers, such as Pfizer, insisted they need 75 years of data before releasing results to the public, the “adverse events” of the public subjects are being tracked and published in medical journals, even if not widely reported.
In any true experiment, there are two groups: the cases and the controls. All subjects who consented, received vaccine lots coded by color and number. Did they receive a vaccine with a Red cap or blue cap? Did they receive saline solution or the COVID spike protein? Did they go from a “fully vaccinated” to “double boosted? Did they opt out?
Let The Experiment Continue!
They say a picture is worth a thousand words, even if the subject matter, a spike protein, has never been officially isolated, or seen with the naked eye. As of this writing, there is no proof the cause of COVID exists.
Since no quantified virus isolates of the 2019-nCoV were available for CDC use at the time the test was developed and this study conducted… — CDC 2109 document
Even without proof, millions of people eagerly jumped aboard The Spike Protein Train to protect themselves with a mask, based on an image of a virus they believed in.
Then, by design, came the vaccines. A vaccine has always been the response to a government-declared pandemic. Recall the 1976 Swine Flu and the 1918 Spanish Flu? [See The Making of a Pandemic for more information]. Vaccine deployment is followed by the damage reports.
In any Live Exercise or Experiment, scientists cannot be expected to have any answers now, or possibly ever. Meanwhile, new symptoms to experimental mRNA vaccines create new, “rare” medical diagnoses. A quick search of Pubmed quickly shows that symptoms are the opposite of rare.
With the introduction of vaccines came the subsequent introduction of Vaccine Inflammatory Syndromes. From Autoimmune Inflammatory Syndrome Induced by Adjuvants,(ASIA), to Post Vaccination Inflammatory Syndrome (PVIS), and Multisystem Inflammatory Syndrome (MIS), all related acronyms describe one cause: Vaccine toxicity.
Since the deployment of COVID injections, the new COVID is Long COVID, ranging from back pain to sleep and digestive disorders, that go beyond 6 months. Symptoms also include postural tachycardia syndrome or POTS.
POTS affects the autonomic nervous system, or the parasympathetic nervous system that regulates voluntary and involuntary actions, as well as thinking, communication, and memory. These symptoms have been long studied as conditions of vaccine injury. Therefore, the injected spike proteins that bring on autoimmune-mediated endothelial injuries can also lead to POTS, especially in the lungs, as evidenced by this study in Clin Auton Res.
Simply go to the VAERS database to search and download the data collected from vaccine-induced injuries the government lists on its own website. VAERS data released by the CDC included a total of 7oo,ooo adverse event reports from all age groups following COVID vaccines, including 15,386 deaths between December 14, 2020, and September 17, 2021. Vaccine-injured patients become lifelong customers of pharmaceutical treatments, with doctors and scientists knowing that many will never return to their normal lifestyles.
All patients were treated with non-pharmacologic therapies, and most required pharmacologic therapies. Six to 8 months after COVID-19, 17 (85%) patients had residual autonomic symptoms, with 12 (60%) unable to return to work.
Published mRNA Vaccine Toxicity Studies: Dizziness
Whether by case study, small study, epidemiological study, or case-control study, all studies are ongoing and accumulating. Searching Pubmed by “dizziness or vertigo” and “COVID vaccine” and find dozens of studies. Here are a few:
Among all the symptoms reported, localized pain, generalized weakness, headache, myalgia, chills, fever, nausea, joint pains, sweating, localized swelling at the injection site, dizziness, itching, rash, decreased appetite, muscle spasm, decreased sleep quality, and brain fogging were the most commonly reported symptoms (in descending order of occurrence). Most of the symptoms reported were nonlife threatening.
Vestibular neuritis (VN) is an acute vestibular syndrome that causes acute and spontaneous vertigo due to unilateral vestibular deafferentiation, leading to nausea or vomiting and unsteadiness that can last from days to weeks. Reactivation of latent type 1 herpes simplex virus, autoimmune disorders, and microvascular ischemia are hypothesized to be etiologies.
We reported for the first time a case of neuromyelitis optica spectrum disorder (NMOSD) that developed after the first dose of inactivated virus vaccine for COVID-19. The patient developed mild fever, vomiting, diarrhea, and cough after receiving the first dose of inactivated virus vaccine. Two months later, she experienced dizziness and unsteady walking. MRI scanning of the brain revealed lesions in area postrema and bilateral hypothalamus, typical for NMOSD. Serum antibodies for AQP4, ANA, SSA, SSB, Ro-52, and p-ANCA were positive. The patient was diagnosed as AQP4-positive NMOSD with coexisting systemic autoimmunity.
The most frequently reported adverse events were headache, myalgia, and dizziness. Of the 835 reported deaths after COVID-19 vaccination, 2 vaccine-related deaths were confirmed.
A 67-year-old man who was medicated for hypertension and diabetes was admitted complaining of fever, maculopapular rash, diarrhea, headache, chills, and dizziness 6 days after the first vaccination of ChAdOx1 nCoV-19 in Korea. The COVID-19 test was negative but with low blood pressure, leukocytosis, skin rash, pulmonary edema, and increased inflammation markers. His lab findings and clinical course were consistent with those of MIS after COVID-19 vaccination.
The 9 patients had an evoked nystagmus pathognomonic for benign paroxysmal positional vertigo; in the remaining 17 cases, peripheral vestibular dysfunction could be excluded and central disorder may be suggested. Due to the prevalence of nystagmus of non-peripheral origin, a central nervous system involvement could not be excluded.
38% mild side effects were observed from vaccination. Following were the general side-effects: myalgia (18.2%), the feeling of sickness (16%), fever (15.6%), dizziness (7.8%), joint pain (7.4%), chills (4.8%), and flu (4.8%). Following were the common neurological side-effects reported: headache (18.2%), fatigue (16.5%), muscle pain (16%), numbness/tingling (3%), and migraine (2.6%). Nausea and diarrhoea were reported in only 3.5% of respondents.
The three most frequent AEFI recorded were vagal response (30%), anxiety reaction (24%) and dizziness (21%). AEFI were more frequently observed among women [aOR= 2.24 (95%CI= 2.00 – 2.50)], and those with at least one previous disease [aOR= 1.47 (95%CI= 1.22-1.76)].
The most common AEFI was pain/tenderness at the injection site experienced by 59.3% of those who experienced any AEFI followed by headache/dizziness (35.3%), itching/rashes at the injection site (8.1%), nausea/vomiting (5.8%) and fever/chills (4.7%).
The patient was a health care worker, aged 34-year old. Past medical history was unremarkable and had not used heparin. Over the next couple of days after the vaccination, he reported headache, nausea, and dizziness as well as abdominal pain. His general status and the laboratories studies deteriorate quickly by increasing liver enzymes and severe coagulopathy. Clinically he had presented acute hepatic failure. He had been received blood products, prednisolone pulse along with broad antibiotics without benefit. He died on the sixth day.
Herein, we describe a 48 years old man presenting with rapidly progressive cognitive decline and hyponatremia diagnosed with anti LGI1 AE, occurring shortly after the second dose of mRNA COVID -19 vaccine and possibly representing a severe adverse event related to the vaccination.
Are we living out a medical experiment or social/behavioral experiment?
Has the world been Trumped?
The government forever claims that people must plan for rising healthcare costs. In 2019, U.S. medical health spending increased by 4.6% to $3.8 trillion or $11,582 per person. If the U.S. medical system is the best in the world then shouldn’t the numbers be doing down?
Whether the crisis is called The Opioid Epidemic or The COVID Pandemic, it is a Crisis of Humanity. The conclusion is always the same when the requirement for more dollars and more research takes precedence over individual healing and freedom from government tyranny:
Dr. Sam Bailey: On Health Freedom Advocates Who Attack Anyone Who Dares to Question Virus & Germ Theory | How RFK, Jr. Was Recently Drawn Into the Viral Existence Debate
Truth Comes to Light editor‘s note: In the video below, Dr. Sam Bailey talks about specific attacks, coming from within the health freedom movement, on the work of those who are questioning the foundations of virus theory.
At this point, most people in the health freedom movement, not to mention the general population, don’t even know that there is a strong debate about the existence of viruses. But awareness is growing.
The so-called, ‘settled science’ of virology must be looked into carefully because, as Dr. Sam Bailey has stated, virus and germ theory “is a system that can and will be used repeatedly to promulgate fear and compliance in the population.”
Dr. Bailey is careful to emphasize that RFK, Jr. is not one of those attacking the work of those who question virology. In this video she shares a segment from a recent public Q&A session wherein Eric Coppolino asks RFK, Jr. some basic questions, pointing to the fact that SARS-C0V-2 has never been shown to exist outside of imagined computer models.
You will find a transcript below the video with links to referenced articles and papers.
RFK, Jr. has been a tireless campaigner in warning the public about the problems of vaccines. However, with regards to the viral existence problem, he has been reluctant to get involved.
Let’s find out what happened when he was drawn into the debate in a recent Q&A session…
Questioning the existence of viruses can be a risky business, as myself and others have found out. However, once you’ve seen the problems with viral theory, it’s not something that can be unseen. It becomes a realization that much of what you were told is factual is not founded in scientific evidence at all. You start to research the material and find that many of the narratives are driven by industry participants and folklore rather than organic science.
While most probably don’t have a dog in the fight, those defending the virus narrative can get pretty hostile.
However, others such as RFK, Jr. simply appear uneasy about mentioning the virus existence issue.
So let’s find out what happened when one of the champions of the health freedom movement was unexpectedly drawn into the debate.
From the start I would like to make it clear that I consider RFK Jr. an ally in promoting health freedom and autonomy. He is a world leader and raising awareness about the risks and ineffectiveness of many vaccines.
I would also say that he has not been ambiguous with regards to his public statements relating to the existence of SARS-CoV-2 or other viruses. As far as I’m aware, he has stated that he believes such viruses exist. Although, in many cases the risks to health and the necessity for a lot of vaccines have been overstated.
I’d also suggest that the virus existence debate does not mean the current health freedom movement will be fractured as some seem to fear.
I don’t mind if other people believe in viruses and germ theory. However, as we point out in ‘Virus Mania’ that is a system that can and will be used repeatedly to promulgate fear and compliance in the population. Once the fatal flaws in the contagion theory are understood, people no longer buy into any of it and don’t get distracted trying to explain different aspects of the scam.
But before we get into RFK Jr.’s recent statements, there have been a few other prominent health freedom fighters who have made forays into the virus existence debate this year.
One was Steve Kirsch. He has been very outspoken about the dangers of the Covid-19 vaccine. Kirsch has realized that many doctors, governments and pharmaceutical companies are playing a game of deception with the public.
But then, on the issue of virus existence he places his faith in the high priests of virology. In early January this year, he decided to announce in his popular blog that SARS-Cov-2 has been isolated and shown to exist.
First, he smeared Drs. Lanka, Kaufman and Cowan with completely inaccurate portrayals of their work and received a huge backlash from his followers in the comment section. Instead of realizing that he might need to conduct his own research into this topic, he then decided to include Christine Massey and myself in the smears.
In a subsequent article 11 days later, curiously Kirsch suggested that we would not front if a live debate was offered.
Well, I can tell you from a series of emails that took place, which Kirsch was part of, that Drs. Bailey times two [Drs. Mark and Samantha Bailey], along with Stefano Scoglio, Drs. Lanka, Cowan and Kaufman, all volunteered to take part in a live debate with any experts that Kirsch was able to produce.
Instead of admitting that he was in over his head, Kirsch posted a third article the following week, embarrassing himself even further with declarations such as: ‘The reason nobody has purified the virus is there is no need to do so in today’s world where gene sequencing is readily available.’ And, ‘if the virus doesn’t exist, then how can 600 labs across the country find the same sequences for the virus in infected samples.’
These kind of statements indicate he’s unaware of the fundamentals of the virus existence debate.
Kirsch doesn’t see that he relies on other “experts” to inform him on the issue. And my husband Mark has written about why this is not a good idea, outlining the nature of the evidence such experts present in his article ‘Warning Signs You’ve Been Tricked by Virologists‘.
As Kirsch has worked out that people selling vaccines may be misleading people, then we would suggest that he peel back another layer to check whether the pharmaceutical and virology establishment, who have billions of dollars of vested interests, may be misleading people with regards to viruses as well.
And some other information I can give you is that I reached out to Steve after he posted his articles offering him a chance to connect, as well as a complimentary copy of ‘Virus Mania’. But he never responded.
In any case, he seems to have gone quiet on the virus existence front, perhaps because he genuinely thinks it’s […] science. Although I would hope that he has some inkling now that there’s more to this than he thought.
Another interesting smear attack against me from a supposed health freedom fighter came from Dr. Roger Watson, writing for The Daily Sceptic in March this year.
This was surprising on a number of fronts. Firstly, because the website developed out of lockdown sceptics and has the motto “question everything”.
However, it seems that questioning the existence of SARS-CoV-2 and the existence of viruses in general is a bridge too far for the so-called ‘Sceptic’.
Secondly, along with my allies including Andy Kaufman and Kevin Corbett, Watson co-signed the viral challenge letter to Boris Johnson demanding that the British prime minister provide proof of the Covid-19 virus. And, if not, then all measures against the nonexistent virus should be dropped.
Obviously, Watson changed his mind at some point and I’m not clear on why that happened. In any case, I had some fun dismantling Watson’s various allegations in my articles ‘The COVID “Sceptics” Who Spread Viral Dogma‘.
Watson’s article was arguably worse […]
Like Kirsch, Watson did not want to enter into a debate about the topic and couldn’t find anyone to front up in his place either. But at least he responded to our emails.
So, now we get to RFK, Jr., which is a slightly different story, as he has not been involved in any smears against me.
In fact, those of you familiar with ‘Virus Mania’ will know that he wrote an important section for our book titled ‘Greed, Negligence and Deception in the Vaccine Industry’.
RFK, Jr. is certainly aware of the controversy surrounding the existence of HIV. As he outlined in his 2022 publication ‘The Real Anthony Fauci’, our friend Tom Cowan even gets a mention in the book when he says: “The first time that someone — Dr. Tom Cowan, a physician from northern California — suggested to me that HIV was not the sole cause of AIDS, I dismissed the comment as ridiculous.”
However, in Chapter 5, ‘The HIV Heresies’, RFK, Jr. goes on to explain how his own research made him realize that there were major problems with the HIV theory.
He is even aware of The Perth Group and the devastating criticisms of the very existence of an infectious HIV particle. Commenting, “In my conversations with Turner and Papadopulos, and in my reading of their paper, I find their arguments clear and convincing. However, I recognize that there are some fifty thousand articles on AIDS in the scientific literature. A casual novitiate like myself has little chance of unraveling this baroque controversy in a vacuum.”
However, most of RFK, Jr.’s focus in the book is on the fact that Anthony Fauci has been instrumental in controlling the HIV/AIDS model and has ruthlessly suppressed dissenting voices.
My hope is that he will read The Perth Group paper ‘HIV – a virus like no other’ one more time and he’ll see there’s no evidence that a pathogenic particle termed HIV exists. And there is no need to read most of the fifty thousand AIDS articles if they fallaciously assert otherwise.
So what happened on April 24 this year — the fundraising event taking place at the Grand Hyatt Hotel in Greenwich, Connecticut?
During the Q&A session, my friend and journalist extraordinaire, Eric Coppolino, was there to put some key questions about the existence of SARS-CoV-2 to RFK Jr.
So let’s take a listen to the exchange that takes place between the two of them on that Sunday afternoon.
Eric Coppolino:
Hi Bobby. Thank you. Christine Massey in Toronto has amassed 182 responses under various Freedom of Information law requests from institutions, provincial, state, and federal, national governments which all say no one has a sample of SARS-C0V-2 taken from a human. Would you please comment on that?
RFK, Jr.:
Yeah, I really am not qualified to comment on it, but … My inclination if there are people who say that viruses don’t exist, that there is no virus… I don’t, you know, my inclination is that that simply is not, you know, that’s not true.
Dr. Sam Bailey:
At least he has admitted that he is relying on inclination, rather than having looked into the evidence himself as he has done with vaccines.
RFK, Jr.:
I can’t argue with you, and I can’t…I actually, on our list there’s a number of people who make those kind of arguments. And other people on the list server…and these are all very brilliant people, ridicule them and dismiss them, and have them produce a lot of evidence.
Dr. Sam Bailey:
It’s hard to know exactly what he’s talking about here. If it’s the same virology papers we’ve been looking at, it is certainly unclear how this constitutes a lot of evidence. In my experience, they are usually reciting the paper’s title without critiquing the methodology, which is where all the problems are.
RFK, Jr.:
I am kind of amused reading the exchanges and my inclination is that viruses do exist and do make people sick. I could be wrong. It could all be a big hoax, but to me, it seems like viruses are real, and … look, I should have just shut up from the beginning and say I’m not gonna answer that question.
Eric Coppolino:
The governments have said they don’t have a sample.
RFK, Jr.:
…You know what? Actually I saw an email exchange yesterday where somebody made exactly that statement and then ten people jumped on him with examples of where that’s not true.
Dr. Sam Bailey:
This was news to me and I know it was news to Christine Massey, coordinator of the SARS-CoV-2 Freedom of Information Project, who demanded the data from the 10 people on Kennedy’s list who claim to prove that the virus had been isolated.
RFK, Jr.:
…The other thing is, I do know this, when you make a freedom of information request, the freedom of information laws do not require the government agency to do science, or to answer questions, specific questions. What they do is, they, the Freedom of Information laws make it obligatory for the government to give you existing documents. So, if you’re telling the government, “I want you to verify this.” They look at their documents and say, “There’s nothing here to verify it.” It doesn’t mean it’s not true. It means they’ve got nothing. But, listen, again, I am not a … scientist. I don’t pretend to be. I find those arguments interesting. And there’s a guy in California, who I deeply respect, Tom Cowan, who makes those arguments and it really… I can’t answer the question.
Dr. Sam Bailey:
This is another interesting statement and perhaps a chance for RFK, Jr. to reflect on the same battle he faces regarding raising awareness about vaccine problems. The mainstream could dismiss RFK Jr.’s arguments as “not being taken seriously by a lot of other people” because the majority of the medical industry still promote all vaccines. However, ‘appeal to popularity’ is a form of faulty reasoning and has no place in a scientific discussion such as this one.
My experience, and I’m sure Tom Cowan and all others in the movement can attest to, is that the majority of people are simply unaware of this debate and don’t even know that questioning the existence of a virus is a thing. And the individuals and corporations that gain from the virus theory often engage in active suppression of the debate.
Prior to widespread internet usage, dissident authors such as The Perth Group were refused publication opportunities in the medical journals. And in the modern era, material such as mine is banned on all the big tech platforms.
The virus theory was put forward in the late 1800s and, for most of us, it is a revelation to go back through the scientific literature and see the key postulants have not been fulfilled .
One of the most amusing, and perhaps tragic, things you’ll see is websites such as AIDSTruth claiming that the science is settled. In 2015 they announced that they were retiring the website because apparently their work was done. The first sentence of their self-congratulatory announcement shows just how disingenuous they are when they use the term ‘AIDS denialism’, knowing very well that what is in dispute is the HIV/AIDS theory or whether an infectious particle, termed HIV, actually exists.
The group also referred to ‘bumps in the early years of treatment’ which is an obscene way to refer to deaths caused by AZT.
In any case, I wonder if the team might consider resurrecting their website or if they are now too busy working on other projects under organizations such as the World Economic Forum and Johns Hopkins.
I think if they do decide to get back into it, they’ll find that the number of individuals and groups opposing their position on the HIV/AIDS theory has gone up dramatically.
Mike Stone of Viroliegy, put together a collection of some of the websites questioning viral theory. And many of them, including Viroliegy itself, have appeared in the last two years.
All the individuals I have personally spoken with, that have or are currently pointing out the flaws in viral theory, they share a number of things in common. Firstly, they all believed in the viral theory at some stage. But when they investigated it for themselves, something changed their minds. Secondly, they have all paid a price whether being publicly censured, smeared or blocked from working in the professions. Thirdly, they are all incredibly generous with their time and share the knowledge with everyone that is interested. And lastly, and perhaps most importantly, they have a passion for exploring the possibilities and following the scientific trail to wherever it takes them by freeing themselves from the shackles of institutional policies, industry capture and public regulatory bodies.
My feeling is that far more people are moving into the questioning the viral theory camp rather than the other way around.
Who knows. Perhaps now that the door has been opened, RFK. Jr. might take more of a look around.
So that we don’t lose touch please find me at drsambailey.com and sign up for my free newsletter.
James Corbett: I Read Bill Gates’ New Book (So You Don’t Have To!)
In an interview with the National Geographic, Tony Fauci made comments about “alternative views” of the origin of the coronavirus. But he was really talking about all unorthodox medical information:
“Anybody can claim to be an expert even when they have no idea what they’re talking about—and it’s very difficult for the general public to distinguish. So, make sure the study is coming from a reputable organization that generally gives you the truth—though even with some reputable organizations, you occasionally get an outlier who’s out there talking nonsense. If something is published in places like New England Journal of Medicine, Science, Nature, Cell, or JAMA—you know, generally that is quite well peer-reviewed because the editors and the editorial staff of those journals really take things very seriously.”
Right you are, Tony.
So, Tony, here is a very serious statement from a former editor of one of those “places,” the New England Journal of Medicine:
“It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgment of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of The New England Journal of Medicine.” (Dr. Marcia Angell, NY Review of Books, January 15, 2009, “Drug Companies & Doctors: A Story of Corruption)
And here is another one, from the editor-in-chief of the prestigious journal, The Lancet, founded in 1823:
“The case against science is straightforward: much of the scientific literature, perhaps half, may simply be untrue. Afflicted by studies with small sample sizes, tiny effects, invalid exploratory analyses, and flagrant conflicts of interest, together with an obsession for pursuing fashionable trends of dubious importance, science has taken a turn towards darkness…”
“The apparent endemicity of bad research behaviour is alarming. In their quest for telling a compelling story, scientists too often sculpt data to fit their preferred theory of the world. Or they retrofit hypotheses to fit their data. Journal editors deserve their fair share of criticism too. We aid and abet the worst behaviours. Our acquiescence to the impact factor fuels an unhealthy competition to win a place in a select few journals. Our love of ‘significance’ pollutes the literature with many a statistical fairy-tale…Journals are not the only miscreants. Universities are in a perpetual struggle for money and talent…” (Dr. Richard Horton, editor-in-chief, The Lancet, in The Lancet, 11 April, 2015, Vol 385, “Offline: What is medicine’s 5 sigma?”)
Why stop there? Let’s consult a late public-health expert whose shoes Fauci would have been lucky to shine: Dr. Barbara Starfield, Johns Hopkins School of Public Health.
On July 26, 2000, the US medical community received a titanic shock, when Starfield revealed her findings on healthcare in America.
The Starfield review, “Is US health really the best in the world?”, published in the Journal of the American Medical Association (JAMA), came to the following conclusion, among others:
Every year in the US, correctly prescribed, FDA approved medical drugs kill 106,000 people. Thus, every decade, these drugs kill more than a MILLION people.
On the heels of Starfield’s astonishing findings, media reporting was perfunctory, and it soon dwindled. No major newspaper or television network mounted an ongoing “Medicalgate” investigation. Neither the US Department of Justice nor federal health agencies undertook prolonged remedial action.
All in all, those parties who could have made effective steps to correct this ongoing tragedy preferred to ignore it.
On December 6-7, 2009, I interviewed Dr. Starfield by email. Here is an excerpt from that interview.
Q: What has been the level and tenor of the response to your findings, since 2000?
A: The American public appears to have been hoodwinked into believing that more interventions lead to better health, and most people that I meet are completely unaware that the US does not have the ‘best health in the world’.
Q: In the medical research community, have your medically-caused mortality statistics been debated, or have these figures been accepted, albeit with some degree of shame?
A: The findings have been accepted by those who study them. There has been only one detractor, a former medical school dean, who has received a lot of attention for claiming that the US health system is the best there is and we need more of it. He has a vested interest in medical schools and teaching hospitals (they are his constituency).
Q: Have health agencies of the federal government consulted with you on ways to mitigate the [devastating] effects of the US medical system?
A: NO.
Q: Are you aware of any systematic efforts, since your 2000 JAMA study was published, to remedy the main categories of medically caused deaths in the US?
A: No systematic efforts; however, there have been a lot of studies. Most of them indicate higher rates [of death] than I calculated.
Q: Did your 2000 JAMA study sail through peer review, or was there some opposition to publishing it?
A: It was rejected by the first journal that I sent it to, on the grounds that ‘it would not be interesting to readers’!
—end of interview excerpt—
Physicians are trained to pay exclusive homage to peer-reviewed published drug studies. These doctors unfailingly ignore the fact that, if medical drugs are killing a million Americans per decade, the heraldic published studies on which those drugs are based must be fraudulent. In other words, the medical literature is completely unreliable, and impenetrable.
WHICH IS EXACTLY WHAT THE TWO ESTEEMED MEDICAL EDITORS I QUOTED ABOVE—MARCIA ANGELL AND RICHARD HORTON—ARE SAYING.
If you know a doctor who enjoys sitting up on his high horse dispensing the final word on modern medicine, you might give him the quotes from Dr. Angell and Dr. Horton, instruct him to read them, and suggest he get in touch with Angell and Horton, in order to discover what has happened to his profession.
As in: DISASTER.
But please, continue to believe everything Fauci is saying. He must be right about the “pandemic.” After all, he has a very important position, and he’s on television.
So what if his policies have torpedoed the economy and devastated and destroyed lives across the country?
So what if he accepted, without more than a glance, that fraud Neil Ferguson’s computer projection of 500,000 deaths in the UK and two million in the US? In 2005, Ferguson said 200 million people could die from bird flu. The final official tally was a few hundred.
So what?
Fauci has an important position, and he’s on television.
TORONTO: The Justice Centre has engaged lawyer Phillip Millar to represent serving members of the Canadian Armed Forces (CAF) who have declined the Covid vaccine on the basis of health concerns or conscientious objections. One of client, Warrant Officer James Topp, is a member of the CAF reserve force facing the charge of “Conduct to the Prejudice of Good Order and Discipline,” which has the potential to result in Court Martial. The Justice Centre also represents 15 other CAF members facing discipline and possible job loss over mandatory Covid vaccine policies implemented by the military.
Mr. Topp, who has been a serving member of the CAF for 28 years, has gained national headlines for his 4,293 kilometre “Canada marches” walk across the country, in protest of mandatory vaccine mandates, forced quarantines, mandatory testing, and other conditions of employment or provision of services.
Mr. Topp began his march on February 20, the same day police forces began using physical force against unarmed Freedom Convoy protesters in Ottawa. Facing job loss for refusing a Covid shot, Mr. Topp is averaging 30 km a day along the highway. His goal is to reach the Tomb of the Unknown Soldier in Ottawa by June 22.
Mr. Topp says government overreach has spread into all aspects of the personal lives of Canadians. “I’m not here for profit, and I don’t want to be a celebrity, but I need to do something,” Mr. Topp told about 100 supporters in Vancouver, who came out on a cold winter day to see him off on his march. “We need to do something to repair us because we’ve been deeply fractured by what has happened…” He adds, “We have to “ensure our government upholds the laws that support Canada’s Charter of Rights and Freedoms.”
Mr. Millar will represent Mr. Topp and 15 other military members in Federal Court, seeking an injunction against the release of CAF members until their grievances are heard. The Justice Centre maintains that military members are entitled to have their constitutional freedoms such as freedom of religion and conscience protected, as CAF members have fought and served to protect the freedoms of all Canadians.
Mr. Millar is a former full-time Combat Officer in the CAF Infantry, former Assistant Crown Attorney, and experienced trial lawyer who has already successfully sued the Department of National Defence (DND) in the past.
“The mandatory vaccine is a flawed policy based on a stubborn refusal to acknowledge that the underlying justification for the mandate has changed. The government is using the Canadian Armed Forces as a policy arm to promote its vaccine mandates. The policy hurts the operational effectiveness, morale, and integrity of the system,” says Mr. Millar.
He notes that the “military chain of command is fast-tracking the release of service members who refuse to get vaccinated under administrative processes, trampling their rights and denying them due process by sidestepping the proper procedures.”
“The DND cannot claim that service members are disobeying a lawful order and then refuse to allow the issue to be tried in the military justice system where a judge can make a determination if it is in fact a “lawful order”,” adds Mr. Millar.
The government is using a “5F release,” which was never meant to be applied in this manner.
“We cannot let them get away with ruining the lives and careers of dedicated Canadians who serve their country. Our soldiers, sailors and air force personnel deserve more. They are highly trained, and many have served their country for years,” Mr. Millar concludes.
Good day, South Africa. My name is Ricardo Maarman and I’m from the Show Us the Virus movement.
Today is the 28th of April, 2022. It is the very day that our Leave to Appeal to High Court to challenge the negative judgment we had, with the cost order against me, was due. And so this is why I am giving you this update today.
Now before we proceed I just want to give you a background on the case and what has been happening so far.
You see, for the past two years (or more than two years) the president of South Africa, and many other presidents around the world as well — but in particular president of South Africa — came forward and made a claim.
He claimed that there was a virus called SARS-CoV-2 and this virus is causing a pandemic. And because of this, he has to take away all of the rights, or a lot of the rights, of the people of South Africa. And he has to impose these draconian lockdown, tyrannical regulations on the people.
And for the past two years, while he has been doing this, people have said many things.
You know, people have said this and that and the other in the showing their disapproval of what is going on and they’re opposition of what is going.
We at the Show Us the Virus movement have said one thing — can be summed up in one question that we have asked throughout this whole period. And that question is: Show us the virus. Show us the virus!
You make a claim that there is a virus, so show it to us.
And what we are faced with is controlled opposition who are trying to distract people from this question.
The president decided to fight the legal battle against me — a long protracted legal battle — and seemingly using all of his influence in the judiciary and his power to win this battle against me, to prevent me from ever being able to have this question answered.
But I think his silence has answered it already. And his actions. His dismissal.
He’s maneuvering has shown to us what the answer to the question is. There is no virus here.
The media has chosen to ignore what we’re doing, sort of an unofficial ban on this — never covering this court case. Showing anything else but this.
And the controlled opposition has been trying to distract people’s attention away from this. ‘No, that’s not an important question. THIS is more important than that.’ This is what has been happening.
And we have stayed consistent. We have said the same thing. Because when you speak the truth, and when you are focused on the truth, you do not have to change your tune every now and again. And that’s why you’ve heard the very same thing from us time and again. Show us the virus.
And that won’t change. We won’t be deterred. We will grasp onto the truth and we will pursue it no matter what, hell or highwater.
Now, what has happened as far as the case is concerned as I say that on the 28th of April, which is today, 2022, this is when our would Leave to Appeal is due. And we have successfully launched an application to the judge for Leave to Appeal.
But a strange thing has happening again. One week before this, on the 22nd of April 2022, the Constitutional Court dismissed our Rescission Application. Rescission Application is a sort of appeal to the Constitutional Court. And they have dismissed it.
Now, this is very important because the judge has dismissed our Interdict Application in the High Court because she says there was no case in front of the Constitutional Court, there was no appeal, there was no decision and, therefore, she has dismissed the case. And, therefore, she has ordered that I pay punitive cost of the billionaire president and also the pretty wealthy and rich Minister of CoGTA [Co-Operative Governance and Traditional Affairs]. I must pay their legal cost, based on the fact that there is actually no case in front of the Constitutional Court pending.
The fact that the Constitutional Court — one week before the time — has dismissed my decision application without a hearing, is proof that the judge was wrong in her judgment. There was a case pending. There was an appeal pending in the Constitutional Court.
The fact that the Constitutional Court now has dismissed it a week before, it is supposed to have helped their cause but it doesn’t really. I think that is a little bit of miscommunication or there’s a miscoordination because it doesn’t really help their case. It advances ours. It proves, without a doubt, that when the judge made her decision she was factually mistaken. She was legally mistaken.
And that is why we are — we have launched this Leave to Appeal and we are successful with the merits of our case.
You must remember, at the end of the day, we have gone to the courts and we have said to the courts: The president made a claim. He said there’s a virus. We ask him to show the virus.
And the just and legal thing to do would be that he must prove his claim. He who claims must prove it.
The courts have, thus far, been dismissive of this basic and fundamental legal issue. And, as I’ve said, the media has tried to basically ban this, hide this very important, very fundamental, issue from the people of South Africa.
The controlled opposition. Now, who are the controlled opposition?
Controlled opposition are all those who say they oppose the government in this tyranny that the government is perpetrating against the people of South Africa, based on the SARS CoV-2 virus, but they agree with the claim of the government. They also promote the idea that there is a virus. And they feel that any lawsuit, or any case, that has to do with the Show Us the Virus question is not important. Other cases are important that focus on other things.
And I say to you, quite frankly Show Us the Virus is the fundamental issue here. Nothing is more fundamental than that.
Without the virus claimed there would be no pandemic and no other thing that anybody has a problem with.
And so anyone who is trying to say that they oppose the government but they agree with this basic premise is, quite frankly, controlled opposition. And the purpose of what they are trying to do is to distract you from what is really important. You’ll see this controlled opposition sellouts in politics and everywhere else, trying to distract the South African people, divide the South African people. It’s no different here.
And you see it — these kinds of thing pop up every time we release a message or every time that we are in the middle of a case of, there’s efforts to try and distract. Go look at the background and history and you will see the same.
As I’ve told you already, for this simple question Show Us the Virus, the president has chose to fight a legal battle with me for the past two years. The judiciaries tried to dismiss it. A basic premise of justice, they’ve tried to dismiss it.
Now, the fact that we have lodged our Leave to Appeal should show you — and the fact that we are still asking the same question for two years — should show you that we don’t give up easily and that we will not be easily distracted. And that we will not be easily deterred. And the fight is far, far from over.
Now, unfortunately, this is not the first time that this situation is happening in South Africa. It’s not the first time. Previously it was the HIV virus, that supposedly caused the AIDS pandemic. And the media did the same.
Anyone that opposes this is called an AIDS denialist. Anyone who raises any questions is ridiculed and attacked in the media quite viciously.
There was also protected court cases going on. And I’ll explain to you those court cases that went on. And, unfortunately, the result is very similar to what we are seeing today.
But first, there was also controlled opposition then. There was the Treatment Action Campaign that was pushing for pregnant women to receive toxic drugs (nevirapine). They were pretending to be on the side of the people and demanding that the people be given this toxic drug, sort of as a mandatory drug from the pharmaceutical industry that were the beneficiaries of this poisonous drug.
We have the same. Those people today who are controlled opposition for the government and for these people pushing this tyranny on us, they’re doing the same. They say it’s a bioweapon. They say it’s not so bad, but the virus is there. They are advocating people use ivermectin which is a toxic drug. They saying people should use other toxins, many other toxins.
I’m not a doctor. I will not be able to specify all of them. But many, many, many toxins. You can go check it yourself. All of those who claim to be opposing the government but they believe there is a virus or they advocate there’s a virus without providing any proof, they are also advocating toxic drugs.
The same that was happening during the time of the HIV issue as the Treatment Action Campaign did then. There was a … big court case happening then where the government then was challenging and saying no we shouldn’t be giving people nevirapine, it’s a dangerous, toxic drug. Eventually this matter ended up in the Constitutional Court then. And in the Constitutional Court Dr. Sam Mhlongo, he raised the issue to the court that the HIV virus has never been isolated and purified. Basically, the HIV virus was never shown to exist. So, you know, they were basically in their way asking the same question then: Show us the HIV virus.
And the court decided to dismiss Dr. Sam Mhlongo and say no that will not be entertained. The court will not answer such a question. Again, basic premise of justice. They claim there’s an HIV virus. Dr. Sam Mhlongo is asking them — is saying to the court they’ve never proven it. And therefore they should not be giving people toxic drugs like nevirapine if they haven’t proven the virus to exist. And the Constitutional Court dismissed Dr. Sam Mhlongo, as they are now trying to dismiss me again. It’s a repeat of history.
Sadly, soon after this whole debacle, Dr. Sam Mhlongo lost his life in mysterious circumstances — car accident and he lost his life. And this is how dangerous it can be to just ask a simple question.
To demand justice can be deadly when you are facing with such force of tyranny and injustice. And sadly, this is the case with Dr. Sam Mhlongo.
Now, as I’ve explained to you here — now this is twice in a row — that there has been, every time we go to the High Court, where we are supposed to go to the High Court, we are supposed to appeal, then the Constitutional Court issues orders. issues orders that will seemingly be very convenient for the president’s legal team and for the High Court then to to use together to judge against me.
There seems to be … I can’t say very clear. I was not in meetings where I see them discuss, but what I see is that within a week — every time we are going to the High Court, within a week the Constitutional Court comes back with a decision supposedly against us and supposedly in favor of the president. And that can then be used to help the High Court make its decision.
So this is a determined effort to see that the question of Show Us the Virus is never the answered and that I must be, you know, saddled with this legal cost. Because the financial cost would be quite substantial. They haven’t issued the bill yet and so this is hanging over my head. But what can happen here quite easily, if my Leave to Appeal is dismissed, my appeal is dismissed, and then I’m saddled with this cost. And then this could mean that they could see sequestrate me. It could render me to lose all of my assets and to be impoverished. So this is the threat that is hanging here — all because of asking a question. Show us the virus.
So, they are very dangerous, you know, in terms of their power that they wield and the threats that they have. As I’ve said here, Dr. Sam Mhlongo has lost his life… I have the knowledge that he lost his life for asking that question. And I’m asking that question. I’m asking the question for them to show the proof of these virus claims of theirs, including the one that Dr. Sam Mhlongo asked about HIV. And I’m asking in addition to that.
So I’m sure for me asking his question and redoubling that question with another one, with another virus, then I should be very careful about car accidents as well.
And, of course, in addition to this financial threat that they now directing towards me. But I am not deterred. And as I’m sure Dr. Sam Mhlongo was not deterred. That his death, and that if any such similar thing happens to me or loss of property, then my debt, my loss of property — or my death in the event that they do the same kind or try the same kind of thing against me — will be a witness against them, a witness against the tyranny, a witness against their falsehood. It will be a witness against their injustice. Because why should this man lose property? Why should this man lose his life for asking you to show us the virus when you have made this claim. This is the height of injustice.
They are determined to see that I lose these cases.
They are determined to see that I am silenced.
They are determined to ensure, with the help of their controlled opposition, that people’s attentions are directed elsewhere.
I’m saying to South Africa, we have been fooled once by these people and their tactics, their intimidation, they’re controlled opposition, sellouts, etcetera.
They fooled us in the past. We should not allow them to fool us again.
For them, having fooled us in the past, shame on them. But if we allow them to fool us and divide us again, then shame on us.
It is time for us to redouble our efforts. Here at the Show Us the Virus movement we have no intention to submit ourselves to evil or to falsehood. No intention whatsoever.
We will redouble our efforts as this lodging of this Leave of Appeal application has shown you. There has been many attempts to distract you in the meantime.
From my request, I asked you and I said South Africa please support me, please help me. I am facing these kind of threats, financial threats. And there has come a whirlwind, a whirlwind to try and distract you away from helping me away, from supporting this cause and standing for truth and justice.
I ask you not to allow yourself to be distracted like this I ask you to stand with me as I redouble my efforts to fight against this tyranny and oppression.
I will not surrender. And I want to implore you that, don’t think others will come and save you. Our situation will not change unless we change it ourselves.
We have to redouble our efforts. We have to pray and turn to God to help us to defeat this evil. And we have to stand together. And we must ensure that we focus. We stand as one. And we never relented evil. We stop it. We fight it. Whatever stumbling blocks there are, we jump over it. Whatever walls there are, we go through it if we have to.
So please let’s stand together. Support me as much as you can. Support our cause. We still have an uphill battle to fight.
We will let you know how the Leave of Appeal application goes. And after, that we’ll follow the appeal itself in our efforts to see that justice is done and that an unjust court order be overturned.
“Covid ‘vaccines’ caused 20 times as many serious side effects and 23 times as many deaths as all other vaccines in the past 20 years combined.”
This week MEP Christine Anderson (AfD) gave her first speech before the European Union’s new “COVID-19 inquiry committee”. The German MEP condemned the EU’s Covid policies and demanded an investigation into the clear human rights violations under the pretext of combatting a virus.
Anderson railed against the “false claims regarding the safety of the vaccines, their alleged definitive approval, and so-called effectiveness.” The MEP pointed out that the European Medicines Agency (EMA) database shows that in seven months, the Covid “vaccines” caused 20 times as many serious side effects and 23 times as many deaths as all other vaccines in the past 20 years combined.
“Why isn’t that being investigated,” questioned the MEP. She explained that the government’s Covid policies had nothing to do with public health. Instead, it seems it has been “a money-making exercise for the pharmaceutical industry.”
Why were alternative methods to fight Covid not investigated or given to the public, questioned Anderson? Instead, she exclaimed, everything in your whole Covid policy “boiled down solely to: “vaccinate, vaccinate, vaccinate.”
Issues Committee Must Address
Anderson pointed out other issues that the committee must investigate. She first zeroed in on the “implementation of vaccine contracts.” Little information is available on vaccine makers’ contracts due to the committee withholding the information. She questioned how she could “properly do her job as an elected MEP” and educate her constituents without the data.
The massive “restrictions of fundamental rights that are unworthy of a democracy” must also be investigated, exclaimed the MEP. “From job losses, discrimination and marginalization, we have experienced a redefinition of fundamental rights.” According to the new definition, our rights are now privileges to which the government picks and chooses who to grant them.
The MEP demanded answers as to why the committee is not investigating the “marginalization and criminalization of critics” who condemned their “anti-democratic measures.”
She went on to say that it is unacceptable for the World Health Organization (WHO) to sign new contracts with EU member states. As Anderson has previously explained, the WHO is fighting for de facto governing power over EU member states in the event of a pandemic:
Dr. Joseph Yi (StreetMD) with Drs. Tom Cowan, Andrew Kaufman & Mark Bailey: A Response to Claims by Drs. Robert Malone, Peter McCullough & Ryan Cole That SARS-CoV-2 Has Been Isolated & Is a Disease-Causing Virus
Dr Joseph Yi, AKA “StreetMD” asked Drs Bailey, Cowan and Kaufman to respond to Drs Malone, McCullough and Cole’s claims that SARS-CoV-2 has been isolated and shown to exist. Boom!
Dr. Sam Bailey with Eric Coppolino — On the Monumental Task of Documenting & Examining the Covid-19 Chronology: “Knowledge Coming to Light Changes Things”
“Knowledge coming to light changes things.” ~ Eric Coppolino
Recently, I have been fortunate to have connected with the inspiring Eric Coppolino, who is based in New York State.
Eric has an incredible history of exposing scientific fraud and environmental pollution cover-ups. He was one of the first to start investigating the COVID-19 scam and is putting something big together to help all of us who are questioning the narrative.
On April 25th, a federal judge stuck down the mask mandate for mass transit.Part of the reasoning was based on fact that the CDC skipped the otherwise-mandatory public notice and comment period as required by the Administrative Procedures Act (APA). However, the main reasoning was to show that government officials do not recognize the limits of their power. Apparently, neither do the masses.
The ruling sent COVID doomsdayers into panic mode. Federal agencies are creatures of statute and are bound by law to operate within the law imposed by Congress. Agencies are not separate entities that may act as they wish.
Their authority is limited to what Congress grants them. So the CDC is governed by Congress – not by any President – and certainly not by career bureaucrats like Fauci. – Phillip Holloway, Esq
Up until COVID, it was illegal to wear a mask to conceal the face in public, with few exceptions. Under COVID, “the science” reversed the mask laws overnight, illegally. Few people questioned the authority of politicians practicing medicine without a license. Perhaps COVID is a lesson to understand that when “science” enters the political picture, its time to question authority. In other words, public health orders do not trump legal orders.
Science and Freedom Do Not Mix
Contrary to popular belief, the law is not based on the latest “science” because science and law are separate spheres of knowledge. Science cannot prove that something is true. Science tests theories, and explains what is observed under a specific set of conditions. Science is a tool. Like any tool, it is neither good or bad, but it can be used according to the will of the “scientist” who wields it. Science does not reveal truth.
Science cannot give you truth. All it can determine is internal self-consistency” based on data within the confines of time and distance. Everything else must be rejected. —William A. Tiller
Science does not usurp the law. Neither do mandates usurp the law. Mandates are public health policies, made by government agencies who use science and fear to manipulate behavior. Yet, federal agencies have NO authority under the law to tell people how to live when it comes to making health decisions.
For those who claim that science “raises awareness,” realize that awareness exercises do nothing to ensure freedom. Real freedom is preserved outside of science, lest people become slaves to a system that is set up to manipulate and engineer consent (as with mandates). Without true consent, there is only implied consent, the illusion of choice, based on the limited options you are provided. An illusion of choice brings an illusion of freedom.
The federal judge made clear that CDC and government officials violated the APA in issuing the mandate.
Despite the protestations by Fauci to the contrary, the CDC was created by a law, is governed by a law, and must act within the confines of that law. – Phil Holloway, Esq. Twitter
Live Exercise
The COVID exercise is a test of people’s ability to know truths from falsehoods. Did anyone investigate the legality of a mandate… or how it may differ from a man date? Did anyone question the blank package insert of the experimental injections? Did anyone know to separate the science from the law?
Early on, the Secretary of State, Mike Pompeo, disclosed, in the media, that COVID is a “live exercise.” Did anyone notice how the media then went back to its regularly scheduled programming; Tel-A-Vision?
Why did it take so long for the courts to intervene, especially when the CDC mask order was set to expire on May 3? Is this court opinion too little, too late? Many would argue the damage has already been done. People’s lives and minds have been altered. Kids breathed their own carbon dioxide to participate in school. Babies did not see the facial expressions of their parents.
What about the Covidians who continue to sport “the mask” in public places? Do they do it “to protect others” as the media tells them to do? Does the media guilt people into “taking responsibility” by wearing a mask? Is health no longer a personal responsibility? Can Fauci run a mile to help you lose weight? Can your doctor wear a life jacket to keep you afloat?
The law is supposed to protect the rights of people to decide for themselves…… but only if people know the laws! Know this: neither Congress, the CDC, nor the media can legislate choice when it comes to your body.
Stay tuned. The Department of Justice has filed a notice of appeal to the 11th Circuit Court of Appeals. This filing is expected to go nowhere, and do nothing, except to save face, since there was no motion for a stay included in the notice of appeal.
While the mask mandate may have ended, the live exercise continues…
On Saturday, Apr. 9, 2022, American Airlines (AA) flight 1067 departed Denver International Airport for its 1-hour and 46-minute flight to Dallas-Fort Worth (DFW). The nearly $100 million Airbus A321 aircraft and its 200 passengers were under the care of AA Captain Bob Snow, who has been with the company for over 31 years. Immediately after pulling into Gate 6 at DFW, Captain Snow—who was forced to get the COVID jab on Nov. 7, 2021, or lose his job—suffered a life-threatening cardiac arrest in the cockpit and almost died. If the tragic event had happened six minutes earlier, there could have been a mass casualty in the skies.
Swiftly, Captain Snow, who passed out and had to be shocked three times, was rushed to Baylor, Scott, and White Health Center ten minutes away. Thankfully, he survived. Snow, who spent time in the hospital’s Intensive Care Unit and is now home, is confident his heart attack directly resulted from the COVID-19 experimental “vaccine” he was mandated to receive. Tellingly, no one from AA or the airline union called Snow while he was in the hospital or stopped by to visit him. While in the hospital, he recorded a video, stating:
“My name is Bob Snow. I am an [American Airlines] Captain and have been a Captain for a number of years. My total service with the company is over 31 years. On Nov. 7, I was mandated to receive a vaccine. Quite literally, I was told if I did not receive the vaccination, I would be fired. This [order] was from our director of flight. So, under duress, I received the vaccine.
Now just a few days ago, after landing in Dallas, six minutes after we landed, I passed out. I coded. I required three shocks. I had to be intubated. I’m now in ICU in Dallas. This is what the vaccine has done for me. I will probably never fly again, based upon the criteria the FAA establishes for pilots. I was hoping to teach my daughter to fly; she wants to be a pilot. [Now] that will probably never happen, all courtesy of the vaccine. This is unacceptable, and I’m one of the victims.
You can see that this is an actual result of the vaccine for some of us. Mandatory, no questions asked, get the shot, or you’re fired. This is not the American way.”
American Airlines Told Captain Robert Snow to Get Vaccinated or Be Fired!
Remarkably, Captain Snow’s COVID-19 vaccine-related cardiac arrest and the myriad of pilot and flight attendant lawsuits currently underway against COVID mask and vaccine mandates are not being reported by mainstream media. Still, it is a subject that many concerned Americans, including Steve Kirsch, Executive Director of the Vaccine Safety Research Foundation, are paying attention to.
Pilots Are Speaking Up About Adverse Events From COVID Jab
Kirsch, who believes that “vaccine injury cover-up is in the interest of all affected parties (except the flying public),” recently interviewed Josh Yoder of US Freedom Flyers about AA Captain Bob Snow. Yoder, a pilot himself, has been a staunch advocate against “vaccine” mandates in the airline industries.
In the interview, Yoder shared with Kirsch that his group has received hundreds of reports about pilots flying planes while suffering from adverse side effects from the COVID jabs. He also noted that cardiologist Dr. Peter McCullough told him that if the airlines were conducting health screenings, 30 percent of the pilots currently flying would most likely be disqualified due to vaccine-induced heart conditions. Yoder told Kirsch:
“He [McCullough] said that if every vaccinated pilot were to be screened, there would be somewhere around a 30 percent loss in manpower.”
Yoder mentioned that the most prominent health issues reported include chest pains, myocarditis, and pericarditis. He noted that “three vaccinated pilots called him yesterday” and said they’re “currently flying with chest pains.” Another said a cardiologist is treating him. Yoder added that the pilots want to remain anonymous because they don’t want to lose their jobs.
Airline pilot Latane Campbell interview: A pilot’s view of COVID policies
On Dec. 15, 2021, McCullough, joined by other experts, including Robert F. Kennedy, Jr., pathologist Dr. Ryan Cole, and Lt. Col. Teresa Long, M.D., signed a 53-page letter to the Federal Aviation Administration (FAA) and major airlines, urging them to flag all vaccinated pilots and administer D-dimer tests, troponin tests, cardiac MRIs, and EKGs to assess their health.
The letter—noting that pilots have died post-vaccination—describes the side effects suffered by numerous pilots, many of whom have been afraid to report them for fear of being grounded. Some have had to seek medical attention and report their injuries due to the significance of the COVID-19 “vaccine” related adverse event. A professional agricultural pilot explained his horrible ordeal, stating in part:
“I am a 33-year-old husband and father of two young boys. I have been healthy my whole life, with no underlying conditions. I received my first dose of the Pfizer COVID Vaccine on February 1. Within thirty minutes, I developed a severe stabbing headache, which later became a burning sensation in the back of my neck. Two days after my vaccination, I got in my airplane to do a job that would only take a few hours.
Immediately after taking off, I knew that something was not right with me. I was starting to develop tunnel vision, and my headache was getting worse. Approximately two hours into flying, I pulled my airplane up to turn around and felt an extreme burst of pressure in my ears.
Instantly, I was nearly blacked out, dizzy, disoriented, nauseous and shaking uncontrollably. By the grace of God, I was able to land my plane without incident, although I do not remember doing this.”
Cody Flint: 33 Y/O Airline Pilot Develops Brain Swelling, Can No Longer Fly Following Jab
Yoder argued that the overall behavior of the FAA, the airlines, and the pilots’ unions demonstrate a contempt for the safety of the flying public and the well-being of airline employees. Kirsch agrees, adding that we have seen a general tone of “belligerence” from nearly all hospitals towards patients who seek second opinions on vaccine-related injury issues. Yoder told Kirsch that the airline industry seems unwilling to address the potentially catastrophic incident.
Yoder pointed out that “AA is trying to create as much distance between themselves and this incident as possible,” adding, “so are the unions. We can’t even get a response.” Still, according to Yoder, Snow will be speaking out soon. When he does, Yoder warned:
“You’re going to hear some very interesting details that are going to be very damning for American Airlines, the Allied Pilots Association, the FAA, and everyone else involved.”
Steve Kirsch, Full Interview with Josh Yoder re: American Airlines Captain Bob Snow vax injury
The Biden administration’s vaccine mandates purporting to force U.S. military members to take the experimental Covid injections are unconstitutional and, because of the potential for genetic changes, may have implications involving patents and intellectual property, super lawyer Todd Callender tells The New American magazine’s Alex Newman in this episode of Conversations That Matter.
To protect the U.S. military, the rights of troops, and the U.S. Constitution, Callender has joined forces with other attorneys such as Tom Renz to sue the Department of Defense. The case is beyond fascinating, and you won’t want to miss this powerful interview.
Transcript of Dr. Sam Bailey’s introduction, provided by TCTL editor:
Last month, we were fortunate to have microbiologist and colloidal chemistry expert Dr. Robin Wakeling present his analysis of Pfizer Comirnaty under the microscope. Since that time Dr. Wakeling has continued to investigate the injections and is also linked up with other New Zealand teams who have shared their findings with him.
In Part 1 of his analysis, Dr. Wakeling presented the appearances of Comirnaty straight from the vial and has some new information regarding how these complexes form.
But perhaps, more importantly, in this video for the first time he is going to analyze the blood of some Pfizer-injected subjects who have suffered adverse reactions.
He’ll explain what he thinks is happening to the red blood cells and some of the most bizarre images he has ever seen in his long career.
In addition to Comirnaty, the teams have also been investigating recent influenza vaccines under the microscope, with some surprising findings that the officially disclosed ingredient don’t appear to explain.
Dr. Wakeling joins my husband, Dr. Mark Bailey, to present round two of Pfizer Under the Microscope.
OTTAWA: After repeatedly calling on the University of Ottawa (U of O) to end its abusive and discriminatory practices, the Justice Centre is pleased announce that the University has stated it will cancel its mandatory vaccine policy for students as of May 1, 2022.
The Justice Centre represented a pregnant student who was suspended from her university program after deciding against the Covid vaccine. Her doctor advised her that her pregnancy was at high-risk for reasons unrelated to Covid and recommended that she complete her mandatory internship virtually, which was allowed by the curriculum.
However, the University of Ottawa refused to accommodate her, falsely claiming that she was trying to circumvent the vaccination policy and that there were no places available for a virtual internship.
Throughout the process, U of O made little to no effort to find a mutually acceptable solution, the student alleges, and refused to justify its decisions in light of the facts of the case.
“It is clear that the University of Ottawa did not intend to follow the ‘reasonable accommodation’ basic criteria set out by the Supreme Court of Canada more than 15 years ago,” notes Samuel Bachand senior external counsel for the Justice Centre in the province of Québec.
After negotiations and discussions with lawyers from the Justice Centre, the student managed to find a suitable placement for virtual internship on her own, which was finally approved by the University.
“The brazenness and bad faith of the University in this matter are appalling. There are clearly, among the people in authority there, bureaucrats who are willing to sacrifice the mission of their institution to irrational health concerns,” comments Mr. Bachand,
“It is well accepted in the scientific community that the Covid vaccines do not prevent infection or transmission of the virus. There was no basis for the vaccine mandate at the University of Ottawa or any other post-secondary institution given that being vaccinated confers no special status or protection,” concludes Mr. Bachand.
“The snake venom theory by Dr. Bryan Ardis is built upon the interpretation of the unpurified fraudulent
“SARS-COV-2” genome which is itself built upon references to other fraudulent genomes of human and
animal “coronaviruses” created in the very same way. Attempting to claim any connections between the
random A,C,T,G’s in a computer database is a useless and pointless exercise as the RNA that was fabricated
into the genome of a “virus” was never purified, isolated, and proven to physically exist in the first place.
Thus any connections between the protein codes said to belong to a “virus” which are then said to be closely
related to supposed snake “coronaviruses” is immediately invalid.
Using this invalid premise to then claim that people have been poisoned by snake venom in the vaccines,
the drugs, and the water supply is nothing but unsubstantiated science fiction that seems designed to have
a few purposes:
To keep people engaged in the lie that a new disease known as “Covid-19” exists and that there is a
singular cause.
To restore faith in monoclonal antibodies and other toxic alternative treatments.
To use the theory to promote and sell anti-venom supplements.
To divide and distract those questioning the official narrative.
To make the “Truther” community look foolish by falling for loosely tied-together circumstantial
evidence that is easily debunked.”
“My story has never been to create fear, panic, and anxiety about water.” He said he told Peters that he believes “there’s actually a snake venom connection to all of COVID-19, and I think that’s the weapon.” – Dr. Bryan Ardis
Summarizing his theory, Dr. Ardis said, “They are using Krait venom and Cobra venom, calling it Covid-19, you’re drinking it, it’s getting into your brainstem and it’s paralyzing your diaphragm’s ability to breathe.”
I really didn’t want to write this article. I was hopeful that people would easily see right through the unsubstantiated claims of Dr. Bryan Ardis that snake venom is the cause of “Covid.” I was hopeful that people would take the time to research the information presented in support of the snake venom theory to see if it held any merit at all. I thought his whirlwind alternative media tour on the who’s who of questionable sources (including the likes of Stew Peters, Mike Adams, and Infowars) would have people questioning why this theory was allowed to be so heavily promoted so quickly. I thought that the fact that the man who created the “Covid” snake venom theory was actually selling his own anti-venom line of supplements would be enough grounds to be skeptical of his motive and his claims.
It seems I was wrong. Just like the baseless vaccine shedding and gain of function/bioweapons narratives, this new snake venom theory has sadly spread through the “Truther” community like wildfire, with many who rightfully challenge the existence of “viruses” clinging to the idea of a new invisible enemy to defeat. They believe that it must be a new toxin. It can’t possibly be the same factors we have seen each and every year leading to disease. This toxin must be hiding in the vaccines, the drugs, and/or even the very water we drink. What these “Truthers” do not realize is that this very line of thinking gives credibility to the idea of a new disease which requires new treatments in order to combat it. This is exactly what the pharmaceutical companies want you to believe.
However, there is NO NEW DISEASE. There is no need for any new or even existing pharmaceutical interventions to treat the same symptoms of detoxification people go through each and every year. In fact, the current treatments can easily be shown to have led to numerous unnecessary deaths. There is no new threat known as “Covid-19” which is being caused by any one factor. The factors leading to the symptoms of disease people are experiencing are multi-causal as they are every year.
Now this is not to say that the vaccines, the drugs, or even the water supply are free of toxins. These are all sources of toxicity and should be investigated as to their composition and effects on our health. However, the theory that there is one factor in all of these sources, i.e. snake venom, and this one factor is leading to the symptoms of disease people are experiencing is, at present time, completely baseless. And it all begins at the very foundation of the fraudulent genome.
The Fradulent Genome
You take that snake or that serpent and you figure out how to isolate genes from that serpent and get those genes of that serpent to insert itself into your God-given created DNA. I think this is the plan all along, was to get the serpents’, the evil one’s DNA, into your God-created DNA.”
He also said genetic sequence testing done on sick patients in Wuhan found their genetic sequence matched two snakes, the Chinese Krait and King Cobra, not bats.”
From Dr. Ardis’ interview with Mike Adams, he supplied the article “Snakes could be the source of the Wuhan coronavirus outbreak” from CNN as his starting point for the “Covid”/snake connection. Within the article, you can see that this claim originates from the fraudulent genomes:
“The researchers used an analysis of the protein codes favored by the new coronavirus and compared it to the protein codes from coronaviruses found in different animal hosts, like birds, snakes, marmots, hedgehogs, manis, bats and humans. Surprisingly, they found that the protein codes in the 2019-nCoV are most similar to those used in snakes.” https://www.google.com/amp/s/amp.cnn.com/
To anyone who actually researched the creation of the original “SARS-COV-2” genome, it is readily apparent that it is a fraudulent computer-generated creation stemming from the unpurified lung fluid of a single patient. The sequenced material could have come from multiple sources, including host DNA/RNA, bacteria, and microbes/microorganisms. It could have even come from outside contamination. There is no way to tell what the origin of the RNA is or even if it was a single source as no particles assumed to be “SARS-COV-2” were ever properly purified and isolated directly from the fluids of the sick patient before being sequenced. Thus, any relation this fabricated sequence has to any other sequence is invalid as the source was never identified to exist as a physical entity to begin with. Considering that the bat and snake “coronavirus” sequences for which the “SARS-COV-2” sequence was then compared to also come from unpurified sources, it is easy to see that any claims as to the origins of the sequenced material is a horrible foundation to build upon for an origin theory of a nonexistent “virus” and/or disease.
Even if this snake-venom connection was valid, the enzyme phospholipase A2 group IIA or sPLA2-IIA, which Dr. Ardis bases much of his claims on, only has similarities to rattlesnake venom. These peptides are “almost identical” to the venoms of animals and yet they are regularly found in healthy humans and other mammals. From his own source:
Like Venom Coursing Through the Body: Researchers Identify Mechanism Driving COVID-19 Mortality
“Researchers from the University of Arizona, in collaboration with Stony Brook University and Wake Forest School of Medicine, analyzed blood samples from two COVID-19 patient cohorts and found that circulation of the enzyme – secreted phospholipase A2 group IIA, or sPLA2-IIA, – may be the most important factor in predicting which patients with severe COVID-19 eventually succumb to the virus.
The sPLA2-IIA enzyme, which has similarities to an active enzyme in rattlesnake venom, is found in low concentrations in healthy individuals and has long been known to play a critical role in defense against bacterial infections, destroying microbial cell membranes.”
Thus, the snake enzymes are in fact normal human enzymes that are regularly found in healthy individuals. There is no mystery as to why these would be present in a sample. We should be able to put this “Covid” snake venom nonsense to bed right here. However, let’s press on a see what else we can uncover.
Antivenom = Monoclonal Antibodies
One thing I will give Dr. Ardis credit for is spotlighting the connection between the creation of antivenoms with the creation of monoclonal antibodies. The processes for both are very similar and the desired outcome is the exact same: the creation of theoretical antibodies. In the case of snake antivenom, it is normally created by a series of injections of the venom of a snake into an animal and then collecting the blood after a period of time. This is usually done through horses but other animals can be used as the host as well. Thus, the antivenom used for a snakebite victim is typically an injection of horse blood.
Both of these therapies have their basis in animal blood and the creation of the theoretical antibodies. Both are associated with toxic side effects. Sadly, while he was originally right about the fact that monoclonal antibodies are toxic and should not be used to treat the symptoms now collectively known as “Covid,” Dr. Ardis changed his tune when another doctor texted him asking if he would use antivenom for a snake bite:
“Last December, Dr Bryan Ardis received a text message from an Emergency Room physician friend of his that sent him down an unexpected and bizarre rabbit hole that may explain the adverse events from the vaccines that we’ve been reporting. The text read: “Hey Dr Ardis…If you got bit by a rattlesnake, would you go to a hospital and get anti-venom?”
“He says, “I realized, all of a sudden, monoclonal antibodies ARE anti-venom. The Federal Government doesn’t want us using anti-venom. Why are they fighting anti-venom and why are we finding anti-venom works against COVID? Is it not a virus? Is it a venom? This is what I want to know: Is COVID a venom and is this why they don’t want you using monoclonal antibodies?”
Do you see the trick? They want you to equate monoclonal antibodies with antivenom. This is supposed to be an “aha” moment where you realize that there is no way that you would not inject antivenom (i.e. horse blood) into yourself if bitten by a snake. It’s a no-brainer, right? We have all seen the movies where a person is bitten by a venomous snake and quickly dies if not given the antivenom.
If you are willing to accept the injection of horse blood into your body to survive a snake bite, why wouldn’t you also inject the cancer-cell cultured blood of genetically altered mice in order to combat “Covid?”
As Dr. Ardis points out, monoclonal antibodies are essentially antivenom. However, he wrongly states that monoclonal antibodies are an effective therapy. According to a September 2021 Cochrane review of the available studies, they found insufficient evidence to claim that monoclonal antibodies are an effective treatment for “SARS-COV-2:”
Are laboratory-made, COVID-19-specific monoclonal antibodies an effective treatment for COVID-19?
“The evidence for each comparison is based on single studies. None of these measured quality of life. Our certainty in the evidence for all non-hospitalised individuals is low, and for hospitalised individuals is very low to moderate.We consider the current evidence insufficient to draw meaningful conclusions regarding treatment with SARS-CoV-2-neutralising mAbs.”
In other words, the evidence for the usefulness of monoclonal antibodies is non-existent. Unfortunately, the Cochrane Review failed to point out that there are various risks and adverse reactions associated with their use:
Do mAbs have risks?
“Therapeutic mAbs, typically administered by intravenous (IV) infusion, have been a valuable and generally safe treatment option for a variety of conditions for many years. However, they are also known to cause a range of side effects and reactions, which can be immediate or delayed.Serious adverse events associated with mAbs include infusion reactions, acute anaphylaxis, and serum sickness, as well as longer-term complications such as infections, cancer, autoimmune disease, and cardiotoxicity.”
In January 2022, the FDA restricted the use of some monoclonal therapies (Bamlanivimab and Etesevimab) that are authorized against “Covid-19” as they were shown to be ineffective:
Coronavirus (COVID-19) Update: FDA Limits Use of Certain Monoclonal Antibodies to Treat COVID-19 Due to the Omicron Variant
“In light of the most recent information and data available, today, the FDA revised the authorizations for two monoclonal antibody treatments– bamlanivimab and etesevimab (administered together) and REGEN-COV (casirivimab and imdevimab) – to limit their use to only when the patient is likely to have been infected with or exposed to a variant that is susceptible to these treatments.
Because data show these treatments are highly unlikely to be active against the omicron variant,which is circulating at a very high frequency throughout the United States, these treatments are not authorized for use in any U.S. states, territories, and jurisdictions at this time. In the future, if patients in certain geographic regions are likely to be infected or exposed to a variant that is susceptible to these treatments, then use of these treatments may be authorized in these regions.
Monoclonal antibodies are laboratory-made proteins that mimic the immune system’s ability to fight off harmful pathogens such as viruses, like SARS-CoV-2. And like other infectious organisms, SARS-CoV-2 can mutate over time, resulting in certain treatments not working against certain variants such as omicron. This is the case with these two treatments for which we’re making changes today.”
On April 16th, 2022, the FDA revoked the use of Bamlanivimab alone as it’s benefits were shown not to outweigh its risks. Somehow despite this evidence, the FDA still allows for it to be used in combination with Etesevimab, even though they previously revoked their use together in January 2022:
Coronavirus (COVID-19) Update: FDA Revokes Emergency Use Authorization for Monoclonal Antibody Bamlanivimab
“Today, the U.S. Food and Drug Administration revoked the emergency use authorization (EUA) that allowed for the investigational monoclonal antibody therapy bamlanivimab, when administered alone, to be used for the treatment of mild-to-moderate COVID-19 in adults and certain pediatric patients. Based on its ongoing analysis of emerging scientific data, specifically the sustained increase of SARS-CoV-2 viral variants that are resistant to bamlanivimab alone resulting in the increased risk for treatment failure,the FDA has determined that the known and potential benefits of bamlanivimab, when administered alone, no longer outweigh the known and potential risks for its authorized use. Therefore, the agency determined that the criteria for issuance of an authorization are no longer met and has revoked the EUA.
On Nov. 9, 2020, based on the totality of scientific evidence available at the time, the FDA issued an EUA to Eli Lilly and Co. authorizing the emergency use of bamlanivimab alone for the treatment of mild to moderate COVID-19 in adults and pediatric patients (12 years of age and older weighing at least 40 kg) with positive results of direct SARS-CoV-2 viral testing, and who are at high risk for progressing to severe COVID-19 and/or hospitalization. Importantly, although the FDA is now revoking this EUA, alternative monoclonal antibody therapies remain available under EUA, including REGEN-COV (casirivimab and imdevimab, administered together), and bamlanivimab and etesevimab, administered together, for the same uses as previously authorized for bamlanivimab alone. The FDA believes that these alternative monoclonal antibody therapies remain appropriate to treat patients with COVID-19 when used in accordance with the authorized labeling based on information available at this time.”
If the FDA’s confusing revoking of the EUA’s of these monoclonal antibodies has you concerned that you will not be able to use them against an imaginary “virus,” don’t worry. The FDA authorized the use of a new “Omicron-specific” monoclonal antibody called Bebtelovimab on February 11th, 2022. Granted, it still carries the same risks, adverse side effects, and uncertainty over clinical worsening listed for the previously ineffective antibody therapies. From the FDA fact sheet:
Coronavirus (COVID-19) Update: FDA Authorizes New Monoclonal Antibody for Treatment of COVID-19 that Retains Activity Against Omicron Variant
“Possible side effects of bebtelovimab include itching, rash, infusion-related reactions, nausea and vomiting. Serious and unexpected adverse events including hypersensitivity, anaphylaxis and infusion-related reactions have been observed with other SARS-CoV2 monoclonal antibodies and could occur with bebtelovimab. In addition, clinical worsening following administration of other SARS-CoV-2 monoclonal antibody treatment has been reported and therefore is possible with bebtelovimab. It is not known if these events were related to SARS-CoV-2 monoclonal antibody use or were due to progression of COVID-19.”
Coronavirus (COVID-19) Update: FDA Authorizes New Monoclonal Antibody for Treatment of COVID-19 that Retains Activity Against Omicron Variant
Hypersensitivity Including Anaphylaxis and Infusion-Related Reactions: Serious hypersensitivity reactions, including anaphylaxis, have been observed with administration of other SARS-CoV-2 monoclonal antibodies and could occur with administration of bebtelovimab. If clinically significant hypersensitivity reactions occur, discontinue and initiate appropriate supportive care. Infusion-related reactions may occur up to 24 hours post injection. These reactions may be severe or life threatening. (5.1)
Clinical Worsening After SARS-CoV-2 Monoclonal Antibody Administration: Clinical worsening of COVID-19 after administration of SARS-CoV-2 monoclonal antibody treatment has been reported and may include signs or symptoms of fever, hypoxia or increased respiratory difficulty, arrhythmia (e.g., atrial fibrillation, sinus tachycardia, bradycardia), fatigue, and altered mental status. Some of these events required hospitalization. It is not known if these events were related to SARS-CoV-2 monoclonal antibody use or were due to progression of COVID-19. (5.2)
Limitations of Benefit and Potential for Risk in Patients with Severe COVID-19: Treatment with bebtelovimab has not been studied in patients hospitalized due to COVID-19. Monoclonal antibodies, such as bebtelovimab, may be associated with worse clinical outcomes when administered to hospitalized patients with COVID-19 requiring high flow oxygen or mechanical ventilation. (5.3)
It should be fairly clear that, unlike Dr. Ardis’ claims, monoclonal antibodies are not effective, carry numerous risky side effects, and can actually worsen the disease they are supposed to treat. Interestingly, this same risk of dangerous side effects and worsening disease outcomes is associated with snake antivenom as well. From the fact sheet of a commonly used antivenom for rattlesnake bites, we find these admitted side effects:
Rattlesnake Antivenin Side Effects Center
“Rattlesnake Antivenin (antivenin crotalidae polyvalent) is an antivenin product used only to treat envenomation caused by bites of crotalids (pit vipers) including rattlesnakes, copperhead and cottonmouth moccasins, and others. Common side effects of Rattlesnake Antivenin include allergic reactions such as flushing, itching, hives, swelling of the face/tongue/throat, cough, shortness of breath, blue color to the skin, vomiting, and anaphylaxis (severe allergic reaction).”
“Immediate systemic reactions (allergic reactions or anaphylaxis) can occur whenever a horse-serum-containing product is administered. An immediate reaction (e.g. shock, anaphylaxis) usually occurs within 30 minutes. Symptoms and signs may develop before the needle is withdrawn and may include apprehension, flushing, itching, urticaria; edema of the face, tongue, and throat; cough, dyspnea, cyanosis, vomiting, and collapse. There have been isolated reports of cardiac arrest and death associated with Antivenin (Crotalidae) Polyvalent (equine origin) use.”
“Serum sickness usually occurs 5 to 24 days after administration and its frequency may be related to the number of Antivenin vials administered.30 The incubation period may be less than 5 days, especially in those who have received horse-serum-containing preparations in the past. The usual symptoms and signs are malaise, fever, urticaria, lymphadenopathy, edema, arthralgia, nausea, and vomiting. Occasionally, neurological manifestations develop, such as meningismus or peripheral neuritis. Peripheral neuritis usually involves the shoulders and arms. Pain and muscle weakness are frequently present, and permanent atrophy may develop.”
Maybe the use of antivenom to treat a snakebite isn’t the super cure it has been sold to be? Is it possible that, as with many pharmaceutical products and interventions, the antivenom itself is creating the very symptoms it is said to treat? For some further insight, let’s look at a few highlights from an paper from September 2019, right before this “crisis,” which reviewed the use of antivenom and had a few revealing claims about the “anti” toxin. You will see it reiterated that the injection of antivenom created from either horse, sheep, goats, and/or rabbits can cause immediate hypersensitivity and anaphylaxis or a delayed “serum sickness” which can occur weeks after the treatment. It is stated that the antivenom has limited efficacy and can be entirely ineffective based on the geographic location. Improper use of antivenom contributes to increased servere outcomes and the production of antibodies in animals leads to a large number (70%) of immunoglobulins that do not react to snake venom:
Perspective on the Therapeutics of Anti-Snake Venom
3. Current Information in the Design of New Antivenoms
“Currently, the only accepted treatment for snakebite envenomation involves intravenous administration of conventional antivenoms comprising antibodies or antibody fragments derived from the plasma of large mammals (generally horses, but also sheep, goats, or rabbits) that have been previously immunized with non-lethal venomous doses [14,15]. Hyperimmunized animals produce antibodies against the venom proteins and serum is extracted from their blood for the treatment of envenomation [6,16]. Conventional serum therapy aims to bind and neutralize the snake venom proteins [17]. It is a fact that the antivenom allows the body to try to reverse the damage caused by the venom. However, it is known that such therapy can cause problems related to different antivenom characteristics, such as:
Immediate hypersensitivity reaction to the alien immunoglobulins, including anaphylactic and pyrogenic reactions such as chills, rigor, headache, and tachycardia. Delayed antivenom reactions or serum sickness is observed after 8 to 12 days of treatment; these are characterized by cutaneous eruptions, fever, and allergies, among other effects [18];
Limited efficacy of antivenom therapy to protect the affected organ/s against immediate local tissue damage and low stability;
Ineffectiveness of the antivenom due to significant geographic variation in the composition of the venom;
Antigenic reactivity due to the taxonomic diversity of the snakes;
Improper use of the antivenom due to incorrect medical management, which contributes to a high incidence of adverse reactions, a low toxin neutralizing potency, or both.
“Current antibody production faces challenges during the immunization of the animal (equine or ovine), leading to the production of a huge number of antibodies that are not related to the snake venom. Around 70% of the immunoglobulins obtained do not act directly against venom toxins [26]. Despite the abovementioned facts, this is the only FDA approved therapy to treat snake venom.”
A few other studies also point out the severe reactions regularly attributed to the use of antivenom. The first is a study from 2016 which points out that not only are adverse reactions common, they occur at a high rate. It is stated that this is due to poor quality control and manufacturing problems:
Adverse reactions to snake antivenom, and their prevention and treatment
“Antivenom is the mainstay of treatment of snakebite envenoming. However, adverse reactions to snake antivenom that is available are common in many parts of the world where snakebite is prevalent. Both acute (anaphylactic or pyrogenic) and delayed (serum sickness type) reactions occur. Acute reactions are usually mild but severe systemic anaphylaxis may develop, often within an hour or so of exposure to antivenom. Serum sickness after antivenom has a delayed onset between 5 and 14 days after its administration. Ultimately, the prevention reactions will depend mainly on improving the quality of antivenom.”
“The high rate of acute adverse reactions to antivenom is an example of how poor manufacturing and quality control by antivenom producers cause problems for patients and their doctors. This highlights the importance of addressing issues related to poor quality and potentially unsafe antivenom. Ultimately, the prevention of reactions will depend mainly on improving the quality of antivenom. Until these improvements take place, doctors will have to depend on pharmacological prophylaxis as well as careful observation of patients receiving antivenom in preparation for prompt management of acute as well as delayed reactions when they occur.”
This next source is from 2018 and it points out that early antivenoms were unsafe and caused severe life-threatening events. While they now have “acceptable” safety profiles, antivenoms still have varying quality and range from 10% adverse reactions to greater than 50%. This same variation in quality is seen in the production of monoclonal antibodies:
Antivenom therapy: efficacy of premedication for the prevention of adverse reactions
“However, in their initial applications, antivenoms did not exhibit good safety results and could even cause life-threatening side effects [8]. The main reason was that first antivenoms were poorly purified preparations or crude sera. Over the years, for many of the original applications, heterologous serums were replaced by other drugs with better safety profiles, such as antibiotics, vaccines and homologous serums. However, in cases of envenomation by snakes, scorpions or arachnids, antivenoms remain the only effective treatment [4]. Currently, after many improvements, antivenoms exhibit acceptable safety profiles [1, 9, 10]. Nevertheless, antivenom quality still varies widely depending on the producer, while some antivenoms exhibit adverse reaction rates of less than 10%, others have values of greater than 50% [11, 12].”
In is interesting to note that there are many factors that are said to influence the severity of a venomous snakebite including the age, sex, and health of the person bitten as well as the type of snake, the geographical location of the snake, the season the bite occurred in, what the snake ate, and how recently the snake released its venom. Antivenoms themselves have been shown to have varying effects in quality due to the geographical location of the snake which somehow renders the antivenom ineffective and even dangerous in different countries and continents, even against the same type of snake. It is said that this has kept locals from seeking out medical care and sticking to traditional healers:
“Snake venoms are highly complicated. At least 26 separate enzymes have been identified with 10 of these enzymes common to all snake venoms (though in different concentrations). All snake bites are not equal. The quality of venom depends not only on the type of snake but on the season, the geographical region, the age of the snake, and how recently it has released venom previously.”
“A study led by Dr Fry has found that antivenoms produced using snakes from one region may perform poorly or fail completely against the same species of snakes from other regions.
Researchers tested the effectiveness of two African and two Indian saw-scaled viper antivenoms against saw-scaled vipers from 10 regions.
The results showed that the two African antivenoms were only effective against snakes from restricted ranges.
One antivenom performed well against West African saw-scaled vipers and the other performed best against the East African saw-scaled vipers.
The Indian antivenom only worked against saw-scaled vipers from the region where the antidote was produced and failed against toxins from other Indian regions. It failed completely against African saw-scaled vipers.
“These antivenoms are being sold and used interchangeably to treat all saw-scaled viper bites, and in many cases they are not working,” Dr Fry says.
“In Kenya, snakebite deaths have increased dramatically after hospitals switched supplies of a very effective African antivenom with a cheaper Indian variety.”
“This creates a knock-on effect in these communities. It’s hard enough to convince people living in these regions not to go to traditional healers to treat snakebite. And if someone does seek proper medical care but dies because of ineffective antivenom, it will be even harder to convince the next victim to seek out antivenom.”
Viper venom’s lethal evolution
It’s the variety of the saw-scaled viper’s prey, from rodents to insects, that researchers say could be the reason why antivenom from one region might not work in another.
“Antivenom is effective and reliable when venom composition does not vary greatly between individual snakes,” UQ PhD candidate in Toxinology Bianca op den Brouw wrote in an article for The Conversation.
“Unfortunately, the venom composition from saw-scaled vipers varies between populations and is thought to be partly due to an evolutionary adaptation linked to their diet.
“Different saw-scaled viper populations feed on different prey. The physiology of these prey animals differs, and this dictates what makes a toxin effective.
“From a medical perspective, this means that the antibodies in an antivenom may not be able to adequately recognise and fight all the harmful toxins in the venom.”
Maybe the proceeding information on how snakebite antivenoms are created as well as the high rate of adverse events from the antibodies used for antivenom now has you questioning that initial “no-brainer” thought: “Of course I would use antivenom if bit by a snake.” If so, you are on the right track as, based on information from the African Snakebite Institute, in most snake bite cases, antivenom is not used and many snake bites are often unattended and/or unreported. In fact, it is apparently a well-known “myth” (i.e. truth in this case) that the antivenom kills more people than the snake venom itself. Most people (over 80%) never receive antivenom as, like the previous sources stated, it can have disastrous side-effects. Most snake bites do not cause symptoms warranting the use of something so toxic. In fact, snake bite victims are not immediately injected with antivenom and typically are sent home after observation:
“Yet people often have a poor understanding of how it works and there are endless myths about antivenom killing more people than the snake venom itself.”
“Few snakebite victims are treated with antivenom (less than 20 % of those hospitalised after a snakebite) as most victims are not severely envenomated or the bite may be from a snake that is not considered potentially deadly or is not covered by the antivenom (Rhombic Night Adder, Berg Adder and Stiletto Snake). Antivenom is relatively scarce, expensive and can have disastrous side-effects. The biggest danger is an acute allergic reaction (anaphylaxis) or, to a lesser degree, serum sickness that can affect the immune system several days after treatment.”
“Snakebite victims are not automatically injected with antivenom as most of them never experience symptoms severe enough to justify its use. The majority of snakes have control over their venom glands and are quite reluctant to waste their venom on humans. They very often give ‘dry’ bites with no subsequent symptoms of envenomation or the snake might inject a little bit of venom that will cause discomfort or some symptoms but nothing serious. Such patients are usually hospitalised for a day, carefully monitored and then sent home.”
“As already mentioned, some snakebite victims quickly have an allergic reaction to antivenom and this happens in more than 40% of all cases where antivenom is used. Some of those victims go into anaphylactic shock which is a life-threatening medical condition and must be treated with adrenaline. This has to do with the fact that our antivenom is made from horse blood and the allergy is basically an allergy to horse proteins.”
Bill Haast – repeated snake bite victim from the world’s deadliest snakes tragically died at the young age of 100 from natural causes. ?
If snake bites regularly do not cause symptoms and do not require the use of antivenom, are snake bites really as toxic and harmful as we previously thought? Are the dangerous side effects linked to snake bites really just the reactions to having horse blood injected into the body as treatment? Is this another case where the treatment causes the symptoms of disease it was supposed to prevent? If the examples of these next few individuals are taken into consideration, it’s entirely plausible to conclude that we have been misled about the dangers stemming from snakebites in order to cover for the toxic effects of the treatment:
Repeated snake bite for recreation: Mechanisms and implications
“There is a debate in the fatality/immunity due to repeated snake bites in human beings either accidentally or incidentally. Haast and Winer[11] reported complete recovery of a patient without any specific therapy even after bitten by a deadly snake Bangarus Caeruleus[11] and the authors attributed it to cross protection of existing antibody between species of Bangarus and Indian, African and Egyptian cobras, as he had a history of bites from these snakes earlier.”
This snake-man got himself bitten over 200 times to become immune to venom
“Bill Haast, a scientist turned snake-man from America, was bitten at least 173 times by poisonous snakes in his life till mid-2008 of which he was fatally injured about 20 times.”
“In the 1950s, he had few ill-effects and didnt need any anti-venom in spite of the fact that he was bitten by the cobras about 20 times as per the report published in Today I Found Out.“
Man makes deadly snakes bite him 160 times in hunt for human antidote
“An amateur scientist has deliberately endured more than 160 self-inflicted snake bites in a bid to become immune to venom.
Tim Friede is obsessed by finding a human antidote to poisonous snake bites, which kill an estimated 100,000 people every year.
Mr Friede was recently bitten by a taipan and a black mamba, two deadly snakes he keeps at his home in Wisconsin, USA, in addition to his two rattlesnakes and water cobra.
He said he experienced a “real throbbing sensation” but he “felt great” after the bites.
“It really hurts and it swells but that’s it,” he said.”
Poison pass: the man who became immune to snake venom
“A lot has been written about Steve Ludwin, widely known as the man who injects snake venom, and lately his life has turned into a non-stop frenzy of international journalists and film crews revelling in the seeming sheer insanity of it.”
“He’s been shooting, swallowing and scratching venom into his skin from some of the world’s deadliest snakes for 30 years. “Snakes are fucking everywhere. The symbol for medicine is two snakes. They’re ingrained in our brain and DNA,” he tells me, proudly insisting that he hasn’t been ill for decades and has developed “a superhuman immune system”. And it’s tempting to believe him. He does look undeniably fit.”
The Photographer Who Was Bitten by a Black Mamba… and Got the Shot “After several minutes and then hours passed and Laita was still feeling fine — experts recommend heading straight for a hospital, by the way — the crew concluded that Laita didn’t have any venom in his system. The photographer believes that it was either a “dry bite,” when a snake doesn’t release any venom, or that his heavy flow of blood pushed out the venom.”
As can be seen, there are numerous examples of people being deliberately and accidentally bitten by the world’s deadliest snakes who are completely fine and do not require treatment from antivenom whatsoever. Are we to conclude that these people are the lucky few who somehow have amazing super-human “immune” systems that render snake venom ineffective? Or have snake bites and the associated symptoms of venom toxicity been blown out of proportion? Could this be a case where some have had bad reactions to a snake bite just as there are those who have severe allergic reactions to bee stings while the majority of snake bite and bee sting victims come away unscathed? Could this be similar to the supposed rabies cases where the majority of those who were bitten by “rabid” animals actually went on to be just fine without getting the rabies vaccination?
The Treatments Are Worse Than the Disease
It’s very apparent that in the case of monoclonal antibodies and anivenom, the adverse effects of the drugs are actually worse than the supposed diseases they are meant to treat. Could this be due to the fact that, like “viruses,” so-called antibodies have never been properly purified, isolated, and proven to exist? The results of studies using antibodies are regularly unreproducible and irreplicable. It is well-known that antibodies are in fact not as specific as are they are claimed to be and are said to regularly bind to the wrong proteins. Perhaps it is difficult to produce safe and effective products when the entities that are supposed to be produced and supplied in the animal blood are entirely theoretical? Maybe the ridiculous snake venom theory should be viewed in the context that it is a bad idea to be injecting anything, let alone animal blood, into our bodies in an attempt to make ourselves feel better when trusting the body and allowing it to heal is often times the best course of action we can take.
In Summary:
Dr. Bryan Ardis put forth a theory that snake venom is the cause of “Covid-19” primarily based on fraudulent genomic data
The snake connection stems from research linking proteins from the fabricated “SARS-COV-2” genome to bat and snake “coronavirus” proteins
The enzyme phospholipase A2 group IIA or sPLA2-IIA, which Dr. Ardis bases much of his claims on, only has similarities to rattlesnake venom
These peptides are “almost identical” to the venoms of animals and are regularly found in healthy humans and other mammals
Dr. Ardis pointed out that, based on a text, he uncovered the connection between antivenom and monoclonal antibodies and stated that theyare the same thing
He wrongly concluded that monoclonal antibodies are an effective treatment for snake poisons that could be in the vaccines, Remdesivir, and water
According to a Sept 2021 Cochrane Review, their certainty in the evidence for the use of monoclonal antibodies in the treatment of “Covid” for all non-hospitalised individuals was low, and for hospitalised individuals was very low to moderate
They considered the current evidence insufficient to draw meaningful conclusions regarding treatment with “SARS-CoV-2-neutralising” mAbs
Monoclonal antibodies are known to cause a range of side effects and reactions, which can be immediate or delayed
Serious adverse events associated with mAbs include infusion reactions, acute anaphylaxis, and serum sickness, as well as longer-term complications such as infections, cancer, autoimmune disease, and cardiotoxicity
In February 2022, the FDA revised the authorizations for two monoclonal antibody treatments – bamlanivimab and etesevimab (administered together) and REGEN-COV (casirivimab and imdevimab) – to limit their use to only when the patient is likely to have been infected with or exposed to a variant that is susceptible to these treatments
The data showed these treatments are highly unlikely to be active against the omicron variant which is circulating at a very high frequency throughout the United States
These treatments are not authorized for use in any U.S. states, territories, and jurisdictions at this time
Monoclonal antibodies are laboratory-made proteins that mimic the immune system’s ability to fight off harmful pathogens
In April 2022, the U.S. Food and Drug Administration revoked the emergency use authorization (EUA) that allowed for the investigational monoclonal antibody therapy bamlanivimab, when administered alone, to be used for the treatment of mild-to-moderate “COVID-19” in adults and certain pediatric patients
Based on its ongoing analysis of emerging scientific data, specifically the sustained increase of “SARS-CoV-2 viral” variants that are resistant to bamlanivimab alone resulting in the increased risk for treatment failure, the FDA determined that the known and potential benefits of bamlanivimab, when administered alone, no longer outweigh the known and potential risks for its authorized use
Importantly, although the FDA revoked this EUA, alternative monoclonal antibody therapies remain available under EUA, including REGEN-COV (casirivimab and imdevimab, administered together), and bamlanivimab and etesevimab, administered together, for the same uses as previously authorized for bamlanivimab alone
In other words, the use of Bamlanivimab and Etesevimab was revoked as well as the use of Bamlanivimab but they can still be used together as an alternative to Bamlanivimab alone…
For the Omicron-specific Bebtelovimab authorized by the FDA in February 2022, possible side effects include
Itching
Rash
Infusion-related reactions
Nausea
Vomiting
Serious and unexpected adverse events including hypersensitivity, anaphylaxis and infusion-related reactions have been observed with other “SARS-CoV2” monoclonal antibodies and could occur with bebtelovimab
In addition, clinical worsening following administration of other “SARS-CoV-2” monoclonal antibody treatment has been reported and therefore is possible with bebtelovimab
The FDA claims that it is not known if these events were related to “SARS-CoV-2” monoclonal antibody use or were due to progression of “COVID-19”
Treatment with Bebtelovimab has not been studied in patients hospitalized due to “COVID-19”
Monoclonal antibodies, such as Bebtelovimab, may be associated with worse clinical outcomes when administered to hospitalized patients with “COVID-19” requiring high flow oxygen or mechanical ventilation
Antivenom carries the same risks of severe side effects and worsening condition as monoclonal antibodies
The listing for common side effects of Rattlesnake Antivenin include allergic reactions such as:
Flushing
Iitching
Hives
Swelling of the face/tongue/throat
Cough
Shortness of breath
Blue color to the skin
Vomiting, and anaphylaxis (severe allergic reaction)
Immediate systemic reactions (allergic reactions or anaphylaxis) can occur whenever a horse-serum-containing product is administered
There have been isolated reports of cardiac arrest and death associated with Antivenin (Crotalidae) Polyvalent (equine origin) use
Serum sickness usually occurs 5 to 24 days after administration and its frequency may be related to the number of Antivenin vials administered
The usual symptoms and signs are:
Malaise
Fever
Urticaria
Lymphadenopathy
Edema
Arthralgia
Nausea
Vomiting
Occasionally, neurological manifestations develop, such as meningismus or peripheral neuritis
Peripheral neuritis usually involves the shoulders and arms and pain and muscle weakness are frequently present, and permanent atrophy may develop
A 2019 review on antivenom stated that currently, the only accepted treatment for snakebite envenomation involves intravenous administration of conventional antivenoms comprising antibodies or antibody fragments derived from the plasma of large mammals (generally horses, but also sheep, goats, or rabbits) that have been previously immunized with non-lethal venomous doses
It is known that such therapy can cause problems related to different antivenom characteristics, such as:
Immediate hypersensitivity reaction to the alien immunoglobulins, including anaphylactic and pyrogenic reactions such as chills, rigor, headache, and tachycardia.
Delayed antivenom reactions or serum sickness is observed after 8 to 12 days of treatment; these are characterized by cutaneous eruptions, fever, and allergies, among other effects
Limited efficacy of antivenom therapy to protect the affected organ/s against immediate local tissue damage and low stability
Ineffectiveness of the antivenom due to significant geographic variation in the composition of the venom;
Antigenic reactivity due to the taxonomic diversity of the snakes
Improper use of the antivenom due to incorrect medical management, which contributes to a high incidence of adverse reactions, a low toxin neutralizing potency, or both
Current antibody production faces challenges during the immunization of the animal (equine or ovine), leading to the production of a huge number of antibodies that are not related to the snake venom
Around 70% of the immunoglobulins obtained do not act directly against venom toxins
According to a 2016 study, adverse reactions to snake antivenom that is available are common in many parts of the world where snakebite is prevalent
The high rate of acute adverse reactions to antivenom is an example of how poor manufacturing and quality control by antivenom producers cause problems for patients and their doctors
The prevention of reactions will depend mainly on improving the quality of antivenom
According to their initial applications, antivenoms did not exhibit good safety results and could even cause life-threatening side effects
Currently, after many improvements, antivenoms exhibit “acceptable” safety profiles yet antivenom quality still varies widely depending on the producer, while some antivenoms exhibit adverse reaction rates of less than 10%, others have values of greater than 50%
All snake bites are not equal and the quality of venom depends not only on the type of snake but on the season, the geographical region, the age of the snake, and how recently it has released venom previously
A study led by Dr. Fry found that antivenoms produced using snakes from one region may perform poorly or fail completely against the same species of snakes from other regions
The results showed that the two African antivenoms were only effective against snakes from restricted ranges
One antivenom performed well against West African saw-scaled vipers and the other performed best against the East African saw-scaled vipers
The Indian antivenom only worked against saw-scaled vipers from the region where the antidote was produced and failed against toxins from other Indian regionand it failed completely against African saw-scaled vipers
“These antivenoms are being sold and used interchangeably to treat all saw-scaled viper bites, and in many cases they are not working,” Dr Fry said
If someone does seek proper medical care but dies because of ineffective antivenom,it will be even harder to convince the next victim to seek out antivenom
Antivenom is effective and reliable when venom composition does not vary greatly between individual snakes
Unfortunately, the venom composition from saw-scaled vipers varies between populations and is thought to be partly due to an evolutionary adaptation linked to their diet
From a medical perspective, this means that the antibodies in an antivenom may not be able to adequately recognise and fight all the harmful toxins in the venom
There are endless myths about antivenom killing more people than the snake venom itself
Few snakebite victims are treated with antivenom (less than 20 % of those hospitalised after a snakebite
Antivenom is relatively scarce, expensive and can have disastrous side-effects
Snakebite victims are not automatically injected with antivenom as most of them never experience symptoms severe enough to justify its use
Snakes very often give ‘dry’ bites with no subsequent symptoms of envenomation or the snake might inject a little bit of venom that will cause discomfort or some symptoms but nothing serious
Such patients are usually hospitalised for a day, carefully monitored and then sent home
Some snakebite victims quickly have an allergic reaction to antivenom and this happens in more than 40% of all cases where antivenom is used
This has to do with the fact that antivenom is made from horse blood and the allergy is basically an allergy to horse proteins
Haast and Winer reported complete recovery of a patient without any specific therapy even after bitten by a deadly snake Bangarus Caeruleus and the authors attributed it to cross protection of existing antibody between species of Bangarus and Indian, African and Egyptian cobras, as he had a history of bites from these snakes earlier
Bill Haast, a scientist turned snake-man from America, was bitten at least 173 times by poisonous snakes in his life till mid-2008 of which he was seriously injured about 20 times
In the 1950s, he had few ill-effects and didnt need any anti-venom in spite of the fact that he was bitten by the cobras about 20 times
An amateur scientist named Tim Friede deliberately endured more than 160 self-inflicted snake bites in a bid to become immune to venom
Mr Friede was recently bitten by a taipan and a black mamba, two deadly snakes he keeps at his home in Wisconsin, USA, in addition to his two rattlesnakes and water cobra
He said he experienced a “real throbbing sensation” but he “felt great” after the bites
Steve Ludwin, widely known as the man who injects snake venom, has been shooting, swallowing and scratching venom into his skin from some of the world’s deadliest snakes for 30 years
He hasn’t been ill for decades and has developed “a superhuman immune system”
A photographer was bit by the deadliest snake, a Black Mamba, and after hours passed, he was still feeling fine and needed no treatment
The snake venom theory by Dr. Bryan Ardis is built upon the interpretation of the unpurified fraudulent “SARS-COV-2” genome which is itself built upon references to other fraudulent genomes of human and animal “coronaviruses” created in the very same way. Attempting to claim any connections between the random A,C,T,G’s in a computer database is a useless and pointless exercise as the RNA that was fabricated into the genome of a “virus” was never purified, isolated, and proven to physically exist in the first place. Thus any connections between the protein codes said to belong to a “virus” which are then said to be closely related to supposed snake “coronaviruses” is immediately invalid.
Using this invalid premise to then claim that people have been poisoned by snake venom in the vaccines, the drugs, and the water supply is nothing but unsubstantiated science fiction that seems designed to have a few purposes:
To keep people engaged in the lie that a new disease known as “Covid-19” exists and that there is a singular cause.
To restore faith in monoclonal antibodies and other toxic alternative treatments.
To use the theory to promote and sell anti-venom supplements.
To divide and distract those questioning the official narrative.
To make the “Truther” community look foolish by falling for loosely tied-together circumstantial evidence that is easily debunked.
If we are to take the claims of Dr. Ardis seriously that the symptoms associated with snake venom is the true cause of a disease known as “Covid-19,” how does his theory explain for the fact that the antivenom and monoclonal antibody treatments cause the exact same symptoms of the disease they are supposed to treat? How would it be determined that the worsening clinical outcomes after injection are from the snake bites/venom rather than the antivenom/monoclonal antibodies given as treatment? How does his theory account for the numerous instances where people have been deliberately bitten by snakes, injected with the venom of snakes, and drank of the venom of the snakes with little to no harmful effects whatsoever? How does his theory account for the fact that the vast majority of “Covid” cases are asymptomatic and the vast majority of snake bite cases need no treatment at all? There are many holes in this theory which will easily be picked apart to make those who follow it look foolish for having done so.
There is no “SARS-COV-2.” There is no “Covid-19.” There is no new disease nor any new symptoms of disease requiring treatment from vaccines, monoclonal antibodies, Remdesivir, Hydroxychloroquine, Ivermectin, NAC, nor any other treatment. There is no need for any anti-venom supplements.
Beware those who will sell you the cause of the disease and the solution.
In a stunning move – soon to be filed under the “completely lost touch with America” folder – the Biden administration is reportedly planning to appeal the ruling that lifted the COVID mask mandate on travel, just hours after most major airlines and airports (and ground transportation) has dropped their mask rules.
It was evident this was coming earlier in the day after White House spokesperson Jen Psaki warned and Xavier Becerra, Biden’s health secretary, told reporters in Nevada, that “we are right now in the process of deciding, and we likely will appeal that ruling, but stay tuned.”
Jonathan Turley offered some insight before the actual decision was made to appeal if CDC thinks it necessary:
The Administration is going to have a hard time making this cat walks backwards. The cheering of passengers and pilots seemed as much as a communication to the Administration as it was a celebration. A large number of airlines immediately declared the mandate to be dead and unenforceable. It is like throwing a retirement party for an employee before they have decided to go. It is a tad awkward to express doubts when someone is showing you the door.
That is why those cheering videos could have a greater impact on the White House than any CDC or DOJ recommendation. The Biden Administration could still appeal as it has in past such cases. There will certainly be many DOJ lawyers asserting that they could win on appeal on the basis of agency deference. The question is who would tell the public. They may have to wait for the “ding, dong” parties to end.
But, given all that, they decided it was worth it…
Justice Department Issues Statement on Ruling in Health Freedom Defense Fund Inc, et. al. v. Biden, et. al.
WASHINGTON – The U.S. Department of Justice today released the following statement on Health Freedom Defense Fund Inc., et. al. v. Biden, et. al. from spokesman Anthony Colev:
“The Department of Justice and the Centers for Disease Control and Prevention (CDC) disagree with the district court’s decision and will appeal, subject to CDC’s conclusion that the order remains necessary for public health. The Department continues to believe that the order requiring masking in the transportation corridor is a valid exercise of the authority Congress has given CDC to protect the public health. That is an important authority the Department will continue to work to preserve.
“On April 13,2022, before the district court’s decision, CDC explained that the order w’ould remain in effect while it assessed current public health conditions, and that the Transportation Security Administration would extend its directive implementing the order until May 3 to facilitate CDC’s assessment.
“If CDC concludes that a mandatory order remains necessary for the public’s health after that assessment, the Department of Justice wall appeal the district court’s decision.“
So, if the CDC – against all the actual science – concludes that wearing a mask should remain mandatory, instead of leaving it as a personal decision, the Biden DoJ will appeal the ruling that was celebrated by most.
The more we ponder this decision, the more this smells like The DoJ throwing The CDC under the bus. The reason being that The CDC now has to come up with some “science” reason to re-mandate the masks (which we know they can’t) and therefore The DoJ is therefore covered if people try to blame them for not appealing.
And the winner of the most ironic sentence of the day goes to White House spokesperson Jen Psaki, who after relying on court ruling after court ruling to enforce varying levels of health tyranny for the last 15 months, uttered the following in her out-loud voice…
“Public health decisions shouldn’t be made by the courts. They should be made by public health experts.”
Who said the left doesn’t do humor… talking of which…
Babylon Bee has some advice for those still living in fear:
It can be difficult, though, to suddenly see all those triggering human faces after the government coddled you and fed your psychotic delusion and fear for the last two years.
Here are seven ways to cope:
Close your eyes and imagine everyone is wearing a full hazmat suit. – It’s a neat little trick that actually works.
Scream at the sky. – This is a well-known coping mechanism. It works especially well if you record your scream onto your TikTok account.
Play The Sims 4 and manage other people’s lives like you’re an all-powerful god to your heart’s content. – Now you can drown people by surrounding their swimming pools with an impenetrable wall of potted plants. You’re in charge here!
Upgrade to 3 or 4 masks, or just roll around in a giant hamster ball. – Keep upping the number of masks you wear, but if that’s not enough, go the hamster ball route.
Get your pilot’s license and start your own airline. – aIrLiNeS aRe PrIvAtE cOmPaNiEs ThEy CaN dO wHaT tHeY wAnT!
Just remember, we’re all in this together. – It’s just for a little while. It’s a small sacrifice to make. If it saves one toddler from a speech impediment it’s all worth it.
Never go outside again. – Curl up in a ball and live out the rest of your days in the corner of your home, completely safe from COVID.
Bear in mind that nothing is stopping the fearful from ‘masking up’ against the virus…
“you are free to wear masks if you like… if they work, they will protect you, if they don’t why mandate them?”
Presumably there are a number of “political science” reasons for the appeal:
1) “Trump” judge
2) Offering a bone to whatever is left on the ‘Democratic base’ amid the unhinged rantings of the blue-checks on Twitter as the dissonance suddenly strikes that they have been wearing face diapers for 2 years for no reason.
3) Making sure to maintain the role as the “party of science“…
4) …ok we couldn’t think of any more… apart from ‘scream to the sky’
Following a federal judge vacating the federal mask mandate on transportation, the TSA responded, “TSA (Transportation Security Administration) will not enforce its Security Directives and Emergency Amendment requiring mask use on public transportation and transportation hubs at this time.”
Within hours various airlines began notifying customers the mask mandate is gone:
♦ American Airlines – “In accordance with the Transportation Security Administration no longer enforcing the federal face mask mandate, face masks will no longer be required for our customers and team members at U.S. airports and on domestic flights.” (link)
♦ Southwest Airlines – “As a result of this development, effectively immediately, Southwest Employees and Customers will be able to choose whether they would like to wear a mask, and we encourage individuals to make the best decision to support their personal wellbeing.” (link)
♦ Delta Airlines – “Effective immediately, masks are optional for all airport employees, crew members and customers inside U.S. airports and on board all aircraft domestically, as well as on most international flights.” (link)
♦ Alaska Airlines – “Effective immediately, all Alaska Airlines and Horizon Air guests and employees have the option to wear a mask while traveling in the U.S. and at work. Masks are no longer required for travel and will be optional.” (link)
♦ United Airlines – No press release. “Masks are no longer required on domestic flights, select international flights (dependent upon the arrival country’s requirements) or at U.S. airports. More comfortable keeping yours on? Go right ahead… the choice is yours (you look dino-mite either way)!” ~Twitter
Various videos show airline employees in a state of jubilation cheering the announcements.
The professional political left is very sad, apoplectic and filled with anxiety. However, the overwhelming majority are happy. This example again reflects how small that minority of rabid maskers was. Easily a 4:1 ratio. Additionally, with all the major carriers and the TSA making official statements, it would be almost impossible to reinstate the mask mandate now. It’s over.
Plane applauded as the stewardess announced the end of the mandate. She broke into tears as she got to take off her mask for the first time in 2 years pic.twitter.com/WlCpZk30QM
“Ladies and gentlemen, this is your pilot speaking. This is the most important announcement I’ve ever made. The federal mask mandate is over. Take off your mask if you choose!”
A federal judge in Tampa, Florida has vacated the federal transportation mask mandate for planes, trains, buses and public Transportation. [PDF Ruling Available Here]
In essence, U.S. District Judge Kathryn Kimball Mizelle found the CDC exceeded its statutory authority with the mask mandate and violated the rules that guide CDC regulations. After Joe Biden arbitrarily announced the federal transportation mandate, the CDC triggered enforcement of the mask mandate without any required time for public feedback on a new regulation.
Within the ruling, one of the commonsense arguments against the federal mandate was noted. Prior to Joe Biden taking office there was no mask mandate. At the time Joe Biden took office and invoked the mask mandate, there was nothing substantively different in/around the spread of COVID-19 and the mitigation efforts underway.
The federal mask mandate was arbitrary and capricious with no justification from the CDC and no required time for the public to provide feedback. The government’s legal argument was that public feedback, comments on rulemaking, was irrelevant because the mandate was going to be enforced regardless of public opinion. That argument was summarily dispatched by the judge saying, just because the government has a pre-determined outcome in mind does not relinquish them from the obligation to follow the rules.
Sensing they were going to lose the case, remarkably the government lawyers argued that only the original plaintiffs in the lawsuit should be granted relief. Meaning, only the two people who filed the lawsuit should be exempt from the federal mask mandate. That didn’t work.
The federal transportation mask mandate is vacated.
Dr. Tom Cowan on “the Snake Venom Stuff”: Covid Caused by a Specific Snake Venom Is Looking Like Pure Fantasy & Remdesivir Is Definitely Not Snake Venom
Right I can imagine there still may be a lot of questions about the snake venom stuff. And we are still looking into that, so I don’t want to say too much.
For those of you who want something to look at right away, I would say I would check out Amandha Vollmer’s — she did a webinar or talk or something. And if somebody has that they could put that in the chat. So that would be a good place to start.
There’s been a lot of other people who’ve weighed in on that. And all I can say for sure that we found out right now is that remdesivir is definitely not snake venom. And that putting any kind of snake venom in the water and have it orally ingested would probably do nothing. In fact it would do nothing.
And the idea that there’s a covid specific disease caused by a specific poisoning with a specific snake venom is looking like pure fantasy.
But hopefully we’ll have more information about that. In the meantime, there’s some places to check out that really go through this in some detail.
For those interested in the difference between being bitten (or injected) with snake venom and drinking venom (note that this is pure venom, not diluted in a vast water supply), we share this video:
Over the past week or so many people have sent us links to the documentary Watch the Water, a 50 minute interview with retired chiropractor Dr Bryan Ardis, who details his theory that “Covid” is caused by chemicals extracted from snake venom being added to the water supply.
Further, Dr Ardis claims that the same venom-based chemicals are in the vaccines and the drug remisdevir, and that researching the venom connection has already got one scientist killed.
Some notable names in the alternate media are giving it some air time, even Dr Reiner Fuellmich has said he will look into it.
He shouldn’t. It is pure nonsense.
A ridiculous theory that flies in the face of observed reality, supported only by anecdotal evidence, biblical metaphors and clips from an episode of The Blacklist.
But good news, if there IS snake venom in the water Dr Ardis can cure you – just spend 120 bucks on his antidote through his website. That’ll drive the venom right out of you.
They are literally selling snake oil.
The blurb alone tells you this is manipulation:
The plandemic continues, but its origins are still a nefarious mystery. How did the world get sick, how did Covid really spread, and did the Satanic elite tell the world about this bioweapon ahead of time?
Reality check – “The world” DIDN’T “get sick”. “Covid” was NOT a “bioweapon”. It DIDN’T “spread”.
The Powers That Be (PTB) just want you to think all this is true, and these guys are, knowingly or not, helping that along.
The whole thing looks very much like the latest attempt at introducing mainstream COVID fear porn through an “alternative” back door.
The superficial narrative in these cases may vary, but the underlying message is always the same – “Be afraid of COVID, because it is a real thing”
The PTB don’t really care if you’re afraid of a virus, a MANMADE virus, 5G…or snake venom in the water. Just so long as you believe COVID is real, new and deadly
The only really inadmissible thing has always been the truth – COVID is a scam. A pea-and-thimble game on a massive scale. Because you can’t govern through fear if no one is afraid.
Is someone dumping “snake venom” in the water?
Maybe. Who knows. The world is insane.
But it has ZERO to do with the “COVID pandemic” because the covid pandemic was made up.
“Darkness has the ability to cover up; light has the ability to uncover! Darkness is the enemy of truth; light is the friend of truth!
~ Mehet Murat ildan
Sometimes acceptance of obvious truth is so stark and thought to be fraught with treachery, that it is literally ignored by the many; making it more comfortable to remain hidden in madness amidst the shadows of deception and lies. While taking responsibility is the only way forward, fear of the truth often wins out, as reliance on collective ignorance gives the false illusion of safety. This behavior is always severely destructive over time, and any psychological relief always temporary, but much more often than not, it is the easy way out for the non-thinking and frightened societal herd. This natural flaw in the makeup of man is well known by the ruling class, and therefore taken advantage of in order to quell dissent and rebellion while gaining further control.
Considering our recent and current history, this was the tactic used for the entirety of the ‘covid’ scam. So long as voluntary acceptance of state propaganda by the masses prevails, this strategy will continually be used going forward in order to perpetuate the advancement of the takeover of humanity in the name of the “Great Reset.” That brings us to the latest threat by the purveyors of evil who have been allowed to rule without resistance. They claim, as voiced by former Trump appointed director of the CDC, Robert Redfield, that the next wave of monumental death worldwide will be due to a non-existent mystery bird flu. This approach by government to manufactured threats, has been around for a very long time, and in the past has been used to frighten the weak, but it is simply a lie.
Threats of avian bird flu, swine flu, including SARS, among many others, have been weapons of the state meant to accelerate panic where none is warranted for very many years. It is imperative to understand that these toxic concoctions are all manmade in labs using gain of function to create bio-weapons. They are not natural, or some lethal strain that just so-happened to affect birds or other animals by accident, and magically jumped to humans. Even the idea of this is ludicrous. If in fact, any such sickness or disease of these types were actually causing mass death, it would only be due to a purposeful release of a bio-weapon by the state, not any innate strain of a normal malady. Knowing this, how could entire populations continue to be so fooled by propaganda?
In 1997, the CDC said that “avian influenza A(H5N1) viruses first spread from poultry to infect humans in Hong Kong resulting in the deaths of 6 of 18 infected persons.” Because of this, the evil WHO and the U.S. sought to increase pandemic preparedness, obviously knowing that this would be useful indoctrination in order to create panic due to future plans to gain power over society. All of this was aligned with the WHO’s “global framework.”
In 2002, SARS was said to be the new disease to fear, and SARS-CoV was to be the “model for future pandemics.” In March of 2003, the ‘novel’ coronavirus, SARS-CoV, was said to be isolated, a lie, and identified and sequenced by nothing other than PCR, an impossibility. There was even the spectre of a future “catastrophic pandemic,” and investigations of live animal markets, as the supposed first case was found in Hong Kong, and said to be able to spread by infected persons traveling by airplane. Does this sound familiar or suspicious to any thinking individual? Is this not the same exact fraud that took place beginning in 2020, two decades later?
In March of 2006, Michael Chertoff, head of Homeland Security, an obvious expert on bird flu, was worried about a bird flu strike any day. “I can’t predict, but I certainly have to say that we should be prepared for the possibility that at some point in the next few months, a wild fowl will come over the migratory pathway and will be infected with H5N1.”
As far back as 1976, the H1N1 Swine Flu hoax took center stage, as the government and its controlled media propaganda campaign went into high gear in order to create a pandemic fraud so as to mass-vaccinate the U.S. population against a non-existent ‘swine flu.’ This conspiracy was also used as a way to get all ‘vaccinations’ available into every person possible. This led directly to 45 million people getting unnecessary injections. At the time, the CDC stated that 80% of the population needed to be ‘vaccinated,’ just as was sought in the ‘covid’ scam.
Again in 2009, the H1N1 fraud was revived, and another government call for mass ‘vaccination’ was issued. As always, the collusion between national and global ‘health organizations, government and government officials, pharmaceutical companies, and corporate insiders was evident. Nothing today has changed, it has only gotten worse, and in fact, the risk now due to the world takeover plot is much more sinister, and globally structured.
In the distant past, while control was a key factor, money from mass ‘vaccination’ was the primary goal. Today, money is a factor, but control of the minds and bodies of the proletariat herds is the result most desired by the ruling ‘elites.’ In addition, depopulation and eugenic transformation of the rest of society, all by way of controlling and lethal injection of a bio-weapon, is what is needed in order to finish the global takeover agenda.
This is a long-term plot to fool the public into believing and expecting that a future pandemic of epoch proportions is imminent. The very idea that ‘natural’ pandemics are inevitable has long been planned and embedded in the minds of the people. This is a multi-decade brainwashing of the common people in order to prepare them for not only mass sickness and death, but also for acceptance of a global governing body with unlimited power.
The most sought-after goal at this time is mass ‘vaccination,’ but this time is different in that the preferred injections are much more dangerous, much more able to physically and psychologically control large numbers of those who have taken the jab, and cause mass death beyond anything seen before. In order to accomplish such a deadly and evil agenda, the people will need to be fooled once again. They will have to believe the lies, and accept that all the impending deaths due to the weaponized ‘covid’ injections, are in fact due to a fraudulent and purposely crafted plot to place blame on a non-existent ‘virus’ that is being called an “avian bird flu.”
The ‘warning’, or more accurately, the foretelling of mass death by the ruling class, as outlined by the ex-CDC commandant Robert Redfield, is that 800 million to 4 billion of us will die due to some mystery bird flu. When the mass deaths occur, it will not be due to any flu or ‘virus,’ it will be due only to the toxic poison that has been previously injected into billions of unsuspecting, order-following slaves to the state.
What type of contamination might be found in a spiked COVID vaccine?
“A foreign body.”
The lot is being recalled due to a foreign body being found in one vial in the lot manufactured at the company’s contract manufacturing site, ROVI – Moderna and ROVI Pharma Industrial Services
Moderna Pharmaceutical, formerly named ModeRNA Therapeutics, became a public company in 2018, specializing in infectious diseases. Prior to the IPO, AstraZeneca was its third-largest investor.
Moderna’s coronavirus shot, known as “SPIKEVAX,” was said to have been approved by the U.S. Food and Drug Administration (FDA) for adults 18 and older on Jan. 31, 2022. But according the the FDA Factsheet, the shot is still only Emergency Use Authorized or EUA. Not approved!
Since November 2020, two of the 4 Biotech companies working to manufacture mRNA “therapies,” — Johnson & Johnson and AstraZenica — had to halt trials over safety concerns. And now the spotlight shines on Moderna’s mRNA vaccine deployment in Europe.
The contaminated lot in question was manufactured at the ROVI site in Spain, and distributed in Norway, Poland, Portugal, Spain, and Sweden from 13-14 January 2022. Reports tie the recalled batches to the Spanish company, ROVI.
Criminal Acts
Will Moderna be investigated for fraud, product safety, death by vaccine?
In February 2021, US officials investigated and acknowledged a “likely association” between Moderna and Pfizer vaccines and myocarditis in adolescents and young people. Of course, the PREP Act and CARES Act both limit liability for death or serious physical injury resulting from these products. See also Moderna’s disclosure in the SPIKEVAX package insert, referencing Myocarditis and Pericarditis, Section 5.2.
All Phase 3 COVID-19 vaccine trails are ongoing and not due to conclude until late 2022/early 2023. The treatments are currently experimental with only 1 year of short-term data and no long term safety data available.
In November 2020 Dr Andreas Noack, a German chemist and one of the EU’s top graphene experts, released a video explaining that he had discovered graphene hydroxide contained in the COVID-19 experimental treatments. He described how the graphene hydroxide nano structures injected into the human body act as ‘razor blades’ inside the veins of recipients and how they would not show up on an autopsy or normal toxicology tests given their atomic size. On 26th November 2021, just hours after publishing his latest video about graphene hydroxide, he died in suspicious circumstances. [See Summary].
Professor Dr Pablo Campra, University of Almeria, Spain also examined Covid-19 experimental treatments in November 2021 using Micro-Raman Spectroscopy, the study of frequencies. He also confirmed the presence of graphene oxide.
Today’s high drug prices show little has changed since 1963, when The Federal Trade Commission ruled that six of the nation’s largest drug companies were conspiring to fix prices on tetracycline, the most widely used antibiotic. The Kefauver drug hearings confirmed the existence of a national crime syndicate and revealed lax enforcement that continues to this day. Note, one of the “big six” criminals, Wyeth Pharmaceuticals, was absorbed by Pfizer.
Gene Therapy or Gene Reset?
Experts contend that the technology in the Pfizer/BioNTech and Moderna shots are not “gene therapy.” But that is not how the experimental products had first been marketed.
According to a November 2021 article at LifeSiteNews, during the 2021 Global Health Summit in Berlin, Bayer executive, Stefan Oelrich, told fellow “experts” that the mRNA COVID “vaccines” are actually “cell and gene therapy” that would have otherwise been rejected by the public if not for a “pandemic” and favorable marketing.
Oelrich also highlighted the term, “Bio Revolution” as:
a confluence of advances in biological science and accelerating development of computing, automation, and artificial intelligence [that] is fueling a new wave of innovation.
As part of his company’s role for “sustainability” Bayer also pledged to push contraception on 100 million women across the world. This rhetoric fits hand-in-glove with Klaus Schwab’s Socialist plan for the “Great Reset.”
Damage from the mRNA injectables are surfacing. According to an October 2021 study in the American Journal of Cardiology:
Sixty percent of the myocarditis related COVID-19 vaccine cases were associated with the Pfizer-BioNTech vaccine, 33% were associated with the Moderna vaccine, and 7% were associated with the Johnson & Johnson vaccine.
According to a November 2021 abstract published in the Journal Circulation titled, “Observational Findings of PULS Cardiac Test Findings for Inflammatory Markers in Patients Receiving mRNA Vaccines:”
…the mRNA vacs numerically increase all markers previously described by others for denoting inflammation on the endothelium and T cell infiltration of cardiac muscle…
Ignorance Is No Excuse
Ignorance is no excuse in the Age of Information. As more information surfaces, do not expect drug companies to change their criminal ways.
The information is available and viewable for anyone who can do a Google search. Drug companies have subtly disclosed the information if you can read about it here.
If any change will come of these revelations, that change rests with each of us. There are no “good” or “bad” experiences. There is only “experience” from which we all choose to learn more.
Children today are being systematically and deliberately destroyed – both mentally and physically.
We are horrified at the way children were pushed up chimneys in the 19th century. Making children work long, arduous hours was considered normal at the time but the children abused in this way were scarred physically and mentally for life.
Today, we like to think that that sort of cruelty is today confined to those parts of the world where children are employed as slave labour in order to dig out the rare minerals needed to make batteries for electric cars.
And, of course, to the factories where slave labourers make overpriced plimsolls or manufacture mobile phones – all at such a low prices that billionaires can progress up the ladder and become even richer.
We like to think that most countries in the so-called developed world have moved on. We close our eyes to the billionaires growing ever richer on the backs of slave labour children.
Those pulling down statues of 19th century slave traders still buy the electric cars, the mobile phones and the absurd shoes and ignore the uncomfortable truths about how they were made.
In the 19th century, child labour was seen as normal and acceptable. In both physical and psychological terms what we are doing now is even worse.
For no sensible, medical reason our world has been turned upside down and millions of children will never recover. (In Africa, of course, millions of children will die as a result of the lockdowns and deliberately staged global panic.)
There is evidence that as a result of the covid hysteria many children have become withdrawn and frightened of approaching strangers – especially if they are not wearing masks.
A children’s charity has seen a massive rise in the incidence of mental and emotional problems in children under 11 years of age. Children are worried about dying, about their friends and family dying, about their future, about missing school, about loneliness, about future epidemics. The AIDS hysteria of the 20th century has become the covid hysteria of the 21st century.
As a result many are either not eating, or eating too much, and they are not sleeping. Panic attacks are becoming commonplace. A study of 10,000 parents showed that 30% of children were worried about catching the virus and 30% were worried about missing their education. Even more worrying 16% were afraid to leave their homes. More than half of the parents were worried about their children.
And yet deaths among healthy children are so rare that it has been suggested that lightning is a bigger threat to children and that it would make more sense to tell children to wear helmets to protect them against meteors than to recommend that they wore masks or practised social distancing.
Nevertheless, schools introduced masks and social distancing, and many teachers and parents want the restrictions to continue indefinitely – until the very last virus on earth has disappeared.
In Ohio, electronic beams were introduced to track school pupils and to enforce social distancing.
In China, robots have been installed to ensure that children wash their hands properly.
Some schools have installed thermal imaging cameras to see if children have a temperature. (This is entirely pointless).
One educational establishment in the US made a viral tracking app mandatory and students were constantly tracked. Students who turned off the app or tried to leave the campus without permission were expelled.
Under normal circumstances, young children touch and hug one another and derive great comfort from this.
Forcing children to remain isolated has created huge psychological problems. Children from poorer families or where there is an unhappy home life have suffered most. Also, the lack of exercise will result in health problems and obesity.
The problems have been exacerbated by threats that children who do not obey the rules `may kill granny’. (The irony is that their government wants to kill granny with blanket DNR notices in hospitals and care homes and by denying medical treatment to older citizens.) Children have seen adults frightened and as a result child terror has been exacerbated.
Many children have become socio-phobic and are developing OCD.
Figures for suicide are nigh on impossible to obtain but suicide is widely recognised to be a leading cause of death in the 5-19 age group, and one survey showed a 50% increase in suicides in 2020 compared to 2019. I suspect the figure will grow.
In an attempt to escape from reality, children are spending vast amounts of time on the internet. Gaming addiction is becoming an increasing problem with cyberbullying adding to anxiety and depression. Sports and out of school activities have been abandoned or disrupted leading to increased boredom, loneliness and depression.
Equally worrying is the fact that altered behaviour in children will frequently be diagnosed as ADHD and drugs such as Ritalin will be prescribed as a long-term remedy.
All this for an infection which children hardly ever catch and hardly ever transmit.
It’s all madness.
The whole fraud was deliberately designed by billionaires and their evil supporters.
And although politicians, their advisors and the medical establishment are guilty of mass genocide for the part they have played, parents and school teachers must also be held responsible.
If parents and teachers had done a little research, they would have known (and would know) that the covid-19 scare is fraudulent.
Their children’s lives have been sacrificed for nothing.
Last week we reported over 4000 police officers are slated to have their religious exemptions to vaccination denied and they will eventually be fired. Yesterday NYPD sources told us nearly 180 police officers had their exemptions officially denied and will be fired within 7 days if they don’t get vaccinated or voluntarily retire. If an officer is fired they give up all rights to their pension and are left with nothing.
These denials were announced the same day 18 people were shot by a gunman in NYC subways and there was not a single transit officer to be found on the scene.
The number of 4,000 we reported last week was incorrect. It is actually 4,875 cops and 1,112 civilians at NYPD that are currently unvaccinated, according to reliable sources in the NYPD. These officers and employees are currently working everyday with a weekly testing option in effect. All of these numbers are coming from NYPD Officers I am in direct contact with who are following the situation extremely closely because their careers are on the line.
Mayor Eric Adams has effectively admitted all of these NYPD officers and employees are slated to be fired. In an interview on CBS News with Marcia Kramer the following exchange occurred discussing the recent firings of NYC workers for declining covid vacciantion:
MarciaKramer: So, if the money permits, would you ever consider rehiring some of the 1,400 people who’ve lost their jobs because they refuse to get the COVID vaccine. Because it looks to me like given the fact that there’s about 5,000 others who have asked for exemptions and didn’t get them and now are appealing, that you could lose a lot more people including a large number of police, fire, and emergency service workers...
Mayor Adams: Well, people should really understand the numbers, the overwhelming number of civil service and city workers. They complied. Under the second wave that we just saw, we did not lose any police officers-
Kramer: You’re about to.
Mayor Adams: I’m sorry?
Kramer: I think you’re about to, because their appeals are now being denied.
Mayor Adams: No, I am hoping that they are smart enough to know that it is imperative to take the vaccine for themselves and their families …
Kramer: So you’re asking them to change their mind?
Mayor Adams: Yes, I am.
[emphasis added]
***
NYPD employees have no first amendment rights of free speech when it comes to their job. If they speak, they get fired. As police officers are now finally directly facing the loss of their jobs, leaks are starting to come forward:
Look at this reply to Mayor Eric Adams regarding the coming firing of nearly 200 Police Oficers due to religious exemption denials:
We need the mainstream media to hold Mayor Eric Adams accountable. The NYPD has massive staffing shortages already! The city cannot afford losing thousands of police officers.
Last November, 2021, news reports threatened that if people who die of COVID were not vaccinated, their families may not get death benefits they would otherwise have received.
If the only guarantee in life is death, then at least there is life insurance, right?
Wrong! Fast forward to the Post-COVID Era, and the fallout from Emergency Use Authorized (EUA) vaccines. According to Forbes Magazine, if today you choose to receive a COVID-19 injection, it could prevent you from receiving a death benefit from your life insurance.
Say what?
No More Death Benefit
According to an article by Brain Peckford, a recent post-Covid vaccine death in France was ruled to be “a suicide” by a judge, due to the experimental nature of the “vaccine.” The insurance company refused to pay. No death benefit. The article reads:
A wealthy elderly man with a high value Life Insurance policy to the amount of millions of euros… dies from the covid jab. His death as a consequence of being jabbed is not disputed by the doctors, nor his life insurers. The Insurance company refused to pay the policy, citing that the taking of experimental drugs, treatments, etc., is excluded from the policy. The family takes the insurance company to court and they have just lost the case.
The judge stated, “the experimental vaccine side effects are publicised and the deceased could not claim not to have known about them when he voluntarily took the jab. There is no law or mandate in France which forced him to be jabbed. Therefore, his death is essentially suicide”.
Suicide is explicitly excluded from this particular policy and in fact from all life insurance policies in general.
This has been the finding of a major western world court system and there is zero doubt that insurance companies world wide will cite this case as legal fact.
Therefore, if anyone ever challenges you on whether these jabs are experimental or not, and that neither the pharma companies, nor govts, nor anyone else but YOU are responsible for accepting them and if you die, legally you have committed suicide.
No insurance, no payouts, no refunds. You are on your own!
Listen to Dr. Pierre describe the same story and explain the view of the American Council of Life Insurers; that insurance companies may deny payment of death benefit if death results from the experimental COVID injection.
How could this possibly be? One moment the experimental vaccine and the boosters protect you against COVID, but the next moment they do not? One moment you are insured with the injection, but the next moment, you are not? As the French say, “C’est la vie. C’est la guerre!” Meaning? Such is life! That’s war. It can’t be helped!
Changing Narratives
Changing narratives happen by design. Those who own the narrative control the outcome. Moreover, in America, under the Smith-Mundt Modernization Act, the media is free to legally propagandize Americans. The EUA vaccines, once advertised to “save lives by preventing deaths” from COVID-19 coronavirus infections, are now “suicidal.”
In May 2021 it was a different story. According to the American Council of Life Insurers, life insurers could not deny a death benefit because the deceased was vaccinated against COVID-19:
A social media post appears to be behind the spread of entirely false information, suggesting a COVID-19 vaccine could be a factor a life insurer considers in the claims-paying process. The fact is that life insurers do not consider whether or not a policyholder has received a COVID vaccine when deciding whether to pay a claim. Life insurance policy contracts are very clear on how policies work, and what cause, if any, might lead to the denial of a benefit. A vaccine for COVID-19 is not one of them. Policyholders should rest assured that nothing has changed in the claims-paying process as a result of COVID-19 vaccinations.
But good propaganda shifts with the winds. Today’s America is not yesterday’s America. America has been hijacked, morally corrupted, debauched, and sold to the highest bidder.
In fact, if you received the Pfizer/BioNTech, Moderna, or Johnson & Johnson COVID-19 vaccines, you received a vaccine deemed “emergency use authorization” (EUA) from the FDA. No EUA injections are FDA-approved vaccines. Further, the first injections deployed were labelled “experimental.” Thus, participants who consented, without proper Informed Consent, became subjects in an ongoing clinical study. Note: Life insurance companies do not cover experiments.
In other news, if you are unvaccinated and hospitalized, insurance may not pay either. A news release from the University of Michigan states:
“Many insurers claim that it is justified to charge patients for COVID-19 hospitalizations now that COVID-19 vaccines are widely available,” said lead author Kao-Ping Chua, M.D., Ph.D., a health policy researcher and pediatrician at Michigan Medicine and the Susan B. Meister Child Health Evaluation Research Center. “However, some people hospitalized for COVID-19 aren’t eligible for vaccines, such as young children, while others are vaccinated patients who experienced a severe breakthrough infection. Our study suggests these patients could substantial bills.”
To recap: if you are 1) Unvaccinated and hospitalized, or 2) vaccinated pre-death, then life Insurance does not pay what you might expect, if at all.
The Double-edged Sword
Read the article Dissolving a Pandemic of Fear, to understand that this trend first began in distant lands during the summer of 2021 with unusual side effects to the globally-deployed experimental vaccines:
Because of the uncertainties from unauthorized tests and experimental vaccines, insurance companies in India and Korea are limiting what they will cover if someone becomes sick from the COVID injections:
Contrary to popular perception, existing health insurance policies are unlikely to cover the cost of vaccination and adverse reactions, if any. Only policies designed purely for the COVID vaccination process — there is none at the moment — will cover the costs.
If you consented to an EUA injection, your life insurance policy has changed. You can’t win for losing, and you can’t claim your life insurance for dying. Something that cuts both ways is known as a double-edged sword.
Justice Through the Courts?
The federal PREP Act and CARES Act prevent practically all civil litigation, ranging from COVID “vaccines” to “tests,” to doctors/pharmacists/nurses. All have blanket civil (but not criminal) protections. All prosecutions are 100.0% discretionary, meaning that even if one admits to a criminal (COVID) act, no private citizen has the power to prosecute any alleged criminal act. That power rests solely with the district attorney and attorney generals — not citizens.
What does this mean? ALL prosecutions are political. In other words, The ONLY way to legally challenge all the “COVID” treason is confined to CRIMINAL prosecutions. Evidence proving criminal fraud has been submitted to the appropriate authorities, and yet there have been no criminal prosecutions through the Department of Justice. Why not? Good question.
What about life insurance fraud? Can insurers be prosecuted in the courts if the Life Insurance Council COVID policy is against the policy holder?
In response to a FOIA request, a federal district judge recently ordered Pfizer Inc. to release 55,000 pages of documents each month, after Pfizer claimed it would not disclose any data for 75 years. That means all the Pfizer vaccine data should be made public by the end of September 2022, rather than the year 2097.
Yet, who is in charge of sifting through the flood of information? What are the consequences of learning the truth that was meant to be hidden? No one knows. What about the fact that government appears to be practicing medicine without a license? How could this possibly be?
Because the narrative is always written by those who control the pen, you must do your own research and captain your own ship. Call your insurance company directly. Ask an “expert” if getting the vaccine will affect your life insurance coverage in any way. Ask if future EUA jabs will affect your premiums or payouts.
Then ask yourself if paying those high insurance premiums is worth the outcome in The COVIDIAN Age, or if it is better to put your money elsewhere.
As the World Council for Health (WCH), our partners and allies have already sought to draw attention to, the World Health Organization (WHO) has proposed a global pandemic agreement that will give it undemocratic rights over sovereign people. See the WCH Open Letter in response to this attempted power grab here.
WHO has quietly opened the floor for comments on the agreement but has provided little time to do so ahead of the first round of hearings scheduled for April 12 and 13.
We encourage everyone to share their thoughts with World Health Organization before the deadline.
1. Go to the World Health Organization website to submit a written submission now
Written submissions are short and can be up to 250 words/1250 characters. The deadline for written submissions is 3 pm UTC on Wednesday, April 13.
Submissions must be in response to the provided guiding question: What substantive elements do you think should be included in a new international instrument on pandemic preparedness and response?
The prompt provided by the WHO does not ask the people of the world whether or not they believe a global agreement is necessary. Instead, the organization has decided for itself that this measure is warranted and is asking for input on what people believe should be included in it.
Refrain from making any statements unrelated to the topic at hand; and
Be presented in a respectful manner, free of any profanity, ad hominem attacks, vulgarity, or other inappropriate language.
If participation, spoken or written, does not conform with these requirements, as determined solely by WHO, the participation will not be receivable. This means that WHO may call speakers to order, and/or discontinue speakers’ connections, and elect to not post written statements.
Why do I need to frame my submission using WHO’s provided context?
Because the WHO reserves the right to judge the relevancy of submissions, it is important to respond to the prompt in an appropriate yet constructive manner. As such, the World Council for Health suggests the following elements be addressed:
National and local leadership retain full autonomy, reserving the right to make decisions based on what is best for their own people.
The ability of nations and local municipalities to opt out of any and all portions of the agreement as they see fit, without consequence.
An open and transparent process with the ability for all people of the world to vote on including failsafe measures that will prevent the application of the global agreement in places where a majority of the people do not want it.
Measures that do not allow for influence in the process by any and all pharmaceutical companies or other global health profiteers.
The hearing will be livestreamed here on Tuesday, April 12.
cover image based on creative commons work of Caniceus
Dr. Naomi Wolf at Defeat the Mandates Rally: “You Hurt Our Kids & Watch Out. Because You Have Never Faced the Rage of Thousands of Mothers & Stepmothers”
In an exclusive interview with The Defender, Jeffrey Beauchine said his mother, Carol, knew her Creutzfeldt-Jakob Disease was related to the Moderna shot. Watching her death was like “something you see out of a movie,” he said.
In an exclusive interview with The Defender, Carol’s son, Jeffrey Beauchine, said it was excruciating to watch his 70-year-old mother — who was healthy until she got the vaccine — die from a disease he believes the vaccine caused.
“I’ve seen a lot in my 20 years as a police officer,” Beauchine said. “I’ve seen hundreds of people shot and this affected me more than anything.”
Beauchine said Carol received her first dose of Moderna on Feb. 16, 2021, and didn’t report any complaints. After getting the second dose on March 17, Carol immediately said she “felt different.”
Beauchine said:
“On March 17, she got her second dose and immediately started having reactions to the second dose. She just had this malaise. She just didn’t feel right and said she just felt ‘off.’ She had what she described as pain and burning at the injection site — like someone was tying a hot rope around her arm. Then she explained it as this numbness setting in around the injection site.”
Beauchine said he and his family members didn’t think it was a usual side effect, but they also didn’t think it was unusual.
“We just thought it was a result of the jab working through the system,” Beauchine said. “Then the numbness spread up through her neck and down her left arm.”
The numbness altered Carol’s hearing and spread “down through her hands” until the left hand lost sensation and mobility.
Beauchine said:
“At this point, it was her entire left arm. She started to develop insomnia. She would go a couple of days at a time without sleep and then she was fatigued. This numbness continued to spread. It went down to her hip and moved to her knees, then the entire left side. You could almost bisect her body and the left side was numb and the right side was normal.”
Beauchine said Carol went to the doctors — who initially thought she had suffered a stroke — but her MRI scans were completely normal.
“Nobody could find anything wrong with her so they sent her home,” Beauchine said. “It was almost like reassurance, while at the same time I wondered why they couldn’t.”
Carol then developed tremors in her left arm.
“It was almost like her arm would start jerking involuntarily,” Beauchine said. “Then the tremors moved on to the left leg.”
Beauchine added:
“My mother began to complain that something was wrong with her brain. She said she couldn’t put thoughts together or make sense of things but she could still communicate. Over the phone, you wouldn’t see the altered version of my mom I knew for 44 years.”
Then Carol developed double vision that ultimately led to blindness, and she began to hallucinate.
“She would see herself falling out of the chair and she would physically see herself on the ground,” Beauchine said. “It was weird to understand. She developed a fear of water and would become scared she was near a body of water.”
Doctors believed Carol was suffering from anxiety because of the shot and started treating her for anxiety. Meanwhile, Carol lost the ability to walk.
Beauchine said:
“She was still at home at this time because the hospital couldn’t find anything wrong with her. She was pretty much in a wheelchair. She went from the one who takes care of everybody to my 70-year-old father taking care of her. Then it got too hard for him and during one doctor’s visit they admitted her to see if they could dive into it further.
Beauchine said doctors ran every test “under the sun,” including an MRI, but couldn’t find anything. The only things doctors noticed were the obvious mobility problems on the left side of her body and balance problems.
The doctors also said there was “something off with her cerebellum but they didn’t know what it was,” he added. Carol tried to explain to the doctors that there was something “internally” wrong with her.
“She was then released to a nursing home,” Beauchine said. “It was the first time I saw my mom really sick.”
He said:
“She was in a nursing home where all this COVID was going on and we had to stand outside the window and yell through the air conditioner hole to talk to my mom. She felt defeated and scared, and my father cared for her 18 hours a day — spoon-feeding her — until the end. It just happened so fast.”
Eventually, Carol was able to get into a skilled nursing home, but she deteriorated rapidly.
“She lost the ability to feed herself because she couldn’t get the food on her fork to put it in her mouth,” Beauchine said. “It crushed me because I could see in her eyes without us having any convo, the fear and like she was defeated.”
Beauchine said there were no more good days and his mother lost the ability to communicate.
“By mid-end of July my mom was just a complete rigid person,” he said. “Lips stopped moving. She could only get a couple of syllables out. She would almost be falling out of a wheelchair in a forward position. She couldn’t tell if she was sitting up.”
Beauchine said his mother knew from the very beginning her condition was related to the shot.
“We all knew from the very beginning it was related to the shot, but we didn’t know the future significance of how bad this would get,” Beauchine said. “People have bad reactions all the time but you get over them. She didn’t get over them.”
Beauchine said the doctors didn’t know what to do because “it was just so new.”
“I’m more content with a doctor telling me they don’t know if it’s the shot because there’s no research than the doctors who say it’s definitely not the shot,” he said. “I got more ‘I don’t knows’ than denials.”
By the end of July, Carol’s husband couldn’t wake her up at the nursing home and the family had a meeting and decided their mother needed to go back to the hospital.
Beauchine said:
“When I rounded the corner, I saw my mom and it was like she was like yelling or howling. Her eyes were completely fixed in the open position. Her mouth was stuck in the open position and she had violent tremors that wouldn’t stop. She didn’t understand what was going on. The only way I can put it is a bomb went off inside of her head.
“It was excruciating for all of us. My dad was like a deer in the headlights — a blank look I had never seen before. And I’ve seen a lot of stuff in my life with my job but this was like … a bomb went off in my mom’s head and all of her limbs were convulsing and tremoring.
“It’s like something you see out of a movie. They say with this disease you come to the cliff and it’s just a drop-off and once you drop off you’re able to physically see that dropping point — and you could see it that night.”
Doctors sent Carol to Strong Memorial in Rochester, New York, and within weeks they confirmed she had CJD.
“We didn’t know what CJD was, but we were told it was like mad cow disease but like a different variant or different mode of getting it,” Beauchine said. “Same disease but a different way of getting it.”
Carol’s prognosis was fatal and the family was told she had only days left. Beauchine said a panel consisting of doctors and students who were overseeing Carol’s case were open to the fact they did not know what caused her CJD.
“People were learning and they said ‘we don’t know if this is related to the vaccine or not. We don’t know because the vaccine is new and there weren’t a lot of studies on the vaccine. We won’t know until the long-term.’”
Carol passed away on Aug. 2, 202, from CJD — a condition she did not have prior to receiving her second dose of Moderna a few months earlier. Her doctors filed a report with the Centers for Disease Control and Prevention’s Vaccine Adverse Event Reporting System (VAERS I.D. 2180699).
VAERS is the primary government-funded system for reporting vaccine adverse vaccine reactions in the U.S. According to the CDC’s website, “CDC and [U.S. Food and Drug Administration] clinicians review reports of death to VAERS including death certificates, autopsy and medical records.”
Beauchine confirmed the family has never received any contact from the CDC regarding his mother’s death, and to his knowledge, her doctors haven’t either.
Beauchine said Carol was a relatively healthy person with no previous history of COVID. Her only underlying condition was arthritis.
“She was always taking care of other people and when the whole COVID thing broke out in the media, she wanted to stay protected so she could see her kids and grandkids,” Beauchine said. “She didn’t want to be hindered by the virus, so when the opportunity arose for her age group, she got the first dose with no complaints.”
Beauchine said he also received the COVID vaccine because it was required for his job.
“At the time, there was a little smidgeon of excitement because they had you so feared over COVID-19 and finally there was a little light at the end of the tunnel,” he said. “And it was going to be okay.”
He added:
“I got the vax. My wife got the vax. My father got the vax. My children will never get the vax. I’m not against a COVID-19 vaccine but it takes years and years and years of clinical trials and studies to deem something safe to put in the human body, and that wasn’t done. We all turned a blind eye to it at the time in moments of hope.
“I didn’t know any of this stuff that we know now, and then you come to find out that hydroxychloroquine and ivermectin have been used off label for years, but to get the Emergency Use Authorization (EUA), you have to show there’s no treatment available to be able to give that authorization, so they killed the treatments, gave the EUA, but there’s no liability on their end.
“It’s just scary nobody knew that at the time. If somebody wants to make an informed decision, let them know what they’re up against.”
Beauchine said when he talks to people, or his mother comes up in conversation, everyone seems to know someone who had a very serious reaction to a COVID vaccine.
“I am not an anti-vaxxer. I’m not crazy or anything like that,” Beauchine said. “But if I or my family can do anything to help somebody or inform somebody or even be a statistic that could come to some sort of positive resolution in all of this, so be it.”
He added:
“Watching someone slowly walk this path and their health degrading right before your eyes from day to day over a few months is terrible. It’s awful. No one should have to go through this. We all just felt for my mom the whole time. It affected us all.”
The Defender has received numerous reports of people who died from sporadic CJD after receiving a COVID vaccine — all women who were between the ages of 60 and 70. This includes Cheryl Cohen and Jennifer Deason Sprague.
According to the latest data from VAERS, between December 14, 2020, and April 1, 2022, there were 19 reported deaths due to CJD attributed to COVID vaccines. The majority of cases occurred in the 65 to 75 age range and involved a sudden onset of symptoms.
That should be everyone’s starting point – with everything, really – assume the media is lying and wait for them to prove they’re not.
Always doubt the press.
Always.
Especially when the fates seem to converge and every single item in the “news” herds public opinion in the same direction and serves the same agenda
…which bird flu definitely does.
Food shortages. Soaring poverty. Rationing. The cost of living crisis. They’re all part of the Great Reset agenda.
In pursuit of that agenda, over the last two years, they destroyed small businesses and wrecked the economy, they have driven truckers out of work and broken supply lines, they have started a war between two of the biggest exporters of wheat in the world and driven up the price of petrol and natural gas.
Bird flu fits this pattern perfectly. The price of poultry and eggs is set to skyrocket…and just days before Easter.
We know they just faked a pandemic in humans. You think they can’t – or won’t – do the same for chickens?
Now, maybe some of you still have faith in the headlines, maybe you haven’t developed that spidey sense that lets you just know when something is total bollocks. And maybe we should make an argument, lest we fall victim to the “fact-checkers”.
So, let’s talk evidence for a quick minute.
*
First, let’s talk about how the US government “detects” bird flu outbreaks.
To detect [avian influenza], the US Department of Agriculture oversees routine testing of flocks done by farmers and carries out federal inspection programs to ensure that eggs and birds are safe and free of virus […] using molecular diagnostics such as polymerase chain reaction (PCR) tests – the same method labs use to detect COVID-19 infections.
The USDA does routine testing of poultry farms using PCR tests.
Remind you of anything?
Second, let’s talk about how world governments are handling the “crisis”.
The mainstream media are reporting a “deadly” bird flu outbreak, The Guardian claims [emphasis added]:
US officials believe nearly 24m poultry birds, mostly chickens and turkeys, have died of flu since virus strain identified in February
All mainstream outlets are taking the same line – reporting million of birds dying of flu.
However, The Conversation article quoted above says [emphasis added]:
As of early April, the outbreak had CAUSED THE CULLING of some 23 million birds from Maine to Wyoming”
And this article in The Scientist claims [again, emphasis added]…
So far this season, tens of millions of birds have died of disease OR BEEN CULLED
So, there is some inconsistency here. Essentially, we don’t know how many died of “bird flu”, or how many were culled with “bird flu”.
Sound familiar?
Now, let’s do some simple math to try and clear up the confusion.
We know the press are reporting roughly 24 million poultry deaths in the US.
Well, that’s already 16 million out of our 24 million. Or 67% of the alleged total “killed by the flu” in the US.
So, at least two thirds of the dead birds – and potentially all of them – were killed in culls, and NOT by the flu at all.
And that’s just the US numbers. Other countries are culling too.
France has had two huge culls of poultry, totalling over 11 million birds.
The UK has culled at least 2 million since October, despite detecting just 108 cases by late March.
Governments are killing millions of birds, and these deaths are being blamed on the flu.
*
To sum up, the backbone of this “bird flu” outbreak is:
Routine testing done using unreliable PCR tests, which can be manipulated to create false-positive results.
Linguistic ambiguity over causes of death, and unreliable reporting of casualty numbers.
Governmental over-reactions which “accidentally” make the problem worse.
…seriously, any of this ringing a bell yet?
Bird flu is just like Covid. The same people, telling the same lies, for the same reasons.
We all know where it goes from here.
Just as with everything else, this will lead to more talk of a food crisis. France is already warning of poultry shortages, and since the US is the worlds biggest exporter of eggs and chicken any disruption there has huge knock effects. The price of eggs and chicken is already going up.
Just as with lockdowns, the bird flu “crisis” will hit small local businesses harder and faster than Big Farma giants (we’re already seeing reports of family farms being destroyed).
They are reporting that free-range birds are more at risk from bird flu (what with being allowed to go outside and live like normal birds), so organic sustainable and ethical farming practices will be hit with new rules that don’t apply to corporate meat factories who treat animals as inanimate objects.
Meanwhile, this will be used to further advance the war on meat, boosting both veganism and backers of lab-grown “meat”.
Inevitably they are already talking about a new bird flu vaccine for people and/or birds. In fact, a UK firm announced a new bird flu vaccine for chicks just three days ago. That’s some well-timed research, great work.
Good luck being an “anti-vaxxer” when they make it law to literally inject all your food with spike proteins or experimental mRNA modifiers or who knows what else.
And, of course, if they ever need it to, the “bird flu” can jump from chickens to humans, and we can have a brand new pandemic, just as the former head of the CDC predicted the other day.
Like I said at the beginning, there is no “bird flu” outbreak, it’s just Covid for chickens. Just more building back better. Just more new normal.
It’s all the Great Reset. That’s all there is these days.
Over the past year-plus, athletes across the world have been dropping like flies as they compete in games. If they aren’t passed out cold, they are seen gripping their chests in agony, unable to breathe due to sudden cardiac events that hit in the heat of the competition.
This wave of heart issues is unprecedented, to say the least. Never before have we seen young, healthy, world-class athletes experiencing heart issues en masse like this. It has never happened, ever. Furthermore, the timing of this sweeping phenomenon could not be more relevant, coinciding perfectly with the rollout of the experimental Covid-19 vaccines.
In December nearly 300 athletes reportedly collapsed or suffered cardiac arrests after taking the COVID vaccines.
But it gets worse. Thanks to a new explosive report by OAN that pegs the number of affected athletes in the hundreds.
In all, their investigation found a jaw-dropping 769 men and women who collapsed with heart issues during competition over the past year (between March 2021 and March 2022).
Most shockingly, the average age of those who experienced full-blown cardiac arrest was just 23.
Considering the timing of this never-before-seen issue in healthy athletes, and the universal push for Covid jabs, all signs point to one culprit: the experimental vaccine.
After detailing two recent high-profile cases, in which two tennis players were forced to recuse themselves from last month’s Miami Open, OAN’s Pearson Sharp reviewed their shocking investigation and asked a few pressing questions that should be answered if you are still questioning what is driving these heart issues in young individuals:
“These are just two o more than 769 athletes who have collapsed during a game on the field over the last year. From March of 2021 to March of this year. The average age of the players suffering cardiac arrest is just 23-years-old.
How many 23-year-old athletes were collapsing and suffering heart attacks before this year? Do you know any 23-year-old people who had heart attacks before now?
And these are just the ones we know about. How many have gone unreported? Nearly 800 athletes – young, fit people in the prime of life falling down on the field. In fact, 500% more soccer players in the EU are dropping dead from heart attacks than just one year ago.”
Just in case there is any lingering inclination to call this a coincidence, Sharp sets the record straight.
“Coincidence? When the Pfizer vaccine is known to cause heart inflamation? No. In fact, many doctors treating these players list their injuries and deaths as being directly caused by the vaccine…
This is not a coincidence – healthy teenagers dying after getting the Pfizer injection. Doctors warned the FDA before they released the experimental vaccine that it would ‘almost certainly cause terrible organ damage.’”
The only question left is: when do we see some accountability?
Former CDC Director Robert Redfield has stated that Bird Flu will jump to humans and be highly fatal in the coming “Great Pandemic,” for which C19 was a mere warm-up.
Airplane leaving jet contrails with COVID-19 word inside. Symbolizing the global spread of the coronavirus through global air traffic.
A few months ago, I wrote an article exploring the connection between the symptoms of disease known as “Covid-19” and air pollution. While air pollution is not the only factor currently causing disease, I laid out why I believe that this is the most likely explanation for any perceived increase in respiratory symptoms of disease. I provided a general overview on the problem of air pollution and how it can impact our health and environment. Within the article, I touched upon the issue of persistent contrails, a.k.a. chemtrails, and provided information directly from Government sources admitting the impact that these trails have on our health and environment. Even though this information is readily available to anyone willing to look, there are many out there who still seem to believe that these trails are harmless. They claim that I am promoting nothing but a baseless conspiracy theory.
The fact of the matter is that these trails are admitted to be harmful to our health and environment by both sides of the “chemtrail” debate. There is no conspiracy theory here. This is a FACT. We can speculate as to who is doing this and why but that is ultimately irrelevant. While pollution from automobiles, factories, power plants, forest fires, etc. all contribute to this air pollution health crisis, the harmful effects from the aviation industry are regularly glossed over and/or omitted when this issue is discussed. However, if you dig deep enough and actually search for the information, what can be found to be admitted by official Government sources regarding the health consequences from these trails is very telling and disturbing.
To start with, I want to provide a quick breakdown of the negative health impact of just one component that is admitted to be found within these persistent trails left in the wake of aircrafts. This is known as particulate matter, the most dangerous of which is PM2.5. From the Environmental Protection Agency (EPA), you will see that PM2.5 is a known toxin potentially made up of hundreds of different chemicals that is so small that it can collect deep within the lungs and even enter the bloodstream. It has been associated with cardiovascular and respiratory disease, irritation of the eyes, throat, and lungs, and premature death:
Particulate Matter (PM) Basics
What is PM, and how does it get into the air?
“PM stands for particulate matter (also called particle pollution): the term for a mixture of solid particles and liquid droplets found in the air. Some particles, such as dust, dirt, soot, or smoke, are large or dark enough to be seen with the naked eye. Others are so small they can only be detected using an electron microscope.
Particle pollution includes:
PM10: inhalable particles, with diameters that are generally 10 micrometers and smaller; and
PM2.5: fine inhalable particles, with diameters that are generally 2.5 micrometers and smaller.
How small is 2.5 micrometers? Think about a single hair from your head. The average human hair is about 70 micrometers in diameter – making it 30 times larger than the largest fine particle.
Sources of PM
These particles come in many sizes and shapes and can be made up of hundreds of different chemicals.
Some are emitted directly from a source, such as construction sites, unpaved roads, fields, smokestacks or fires.
Most particles form in the atmosphere as a result of complex reactions of chemicals such as sulfur dioxide and nitrogen oxides, which are pollutants emitted from power plants, industries and automobiles.
What are the Harmful Effects of PM?
Particulate matter contains microscopic solids or liquid droplets that are so small that they can be inhaled and cause serious health problems. Some particles less than 10 micrometers in diameter can get deep into your lungs and some may even get into your bloodstream. Of these, particles less than 2.5 micrometers in diameter, also known as fine particles or PM2.5, pose the greatest risk to health.
Fine particles are also the main cause of reduced visibility (haze) in parts of the United States, including many of our treasured national parks and wilderness areas.”
Health and Environmental Effects of Particulate Matter (PM)
Health Effects
The size of particles is directly linked to their potential for causing health problems. Small particles less than 10 micrometers in diameter pose the greatest problems, because they can get deep into your lungs, and some may even get into your bloodstream.
Exposure to such particles can affectboth your lungs and your heart. Numerous scientific studies have linked particle pollution exposure to a variety of problems, including:
premature death in people with heart or lung disease
nonfatal heart attacks
irregular heartbeat
aggravated asthma
decreased lung function
increased respiratory symptoms, such as irritation of the airways, coughing or difficulty breathing.
People with heart or lung diseases,children, and older adults are the most likely to be affected by particle pollution exposure.
PM2.5 and other particulate matter is only part of the dangerous substances found in these persistent contrails. Other admitted substances include carbon dioxide (CO2), volatile organic compounds (VOC), nitrogen oxides (NOX), sulfur oxides (SOX), black carbon soot, and other trace metals. It is simply beyond logic and reasoning to believe that the inhalation of these substances on a daily basis is not harmful to one’s health.
Recently, some members of Congress were interested in addressing the health and environmental problems associated with aviation. On February 8th, 2022, the Congressional Research Service released a report describing the problem and how to address it. A few highlights showcase that aviation pollution is the fastest-growing pollutant over the past decade and that there are numerous toxic substances found within these trails: Aviation, Air Pollution, and Climate Change
Emissions from Aircraft
“The U.S. Environmental Protection Agency (EPA) estimates that transportation—including passenger cars and light trucks, heavy-duty trucks, buses, trains, ships, and aircraft—accounted for 35% of carbon dioxide (CO2, the principal GHG) emissions in 2018. While CO2 emissions from passenger cars and light trucks exceed those from aircraft in the United States, CO2 emissions from aviation are currently experiencing a faster rate of growth. All aircraft, including military, commercial, and privately chartered, accounted for 13% of the U.S. transportation sector’s CO2 emissions and 5% of all U.S. CO2 emissions in 2018. Commercial aircraft, including those operated by passenger and all-cargo airlines, accounted for 11% of transportation sector and 4% of all emissions. These estimates include emissions from U.S. domestic flights and emissions from international flights departing the United States, referred to as “international bunkering.”
In the United States, aggregate CO2 emissions from aircraft have fluctuated due to changes in technology, the economy, travel frequency, and military activity, among other reasons. However, since the global financial crisis in 2009,aggregate CO2 emissions from all aircraft types have grown steadily, increasing by almost 22% between 2009 and 2018. This increase makes aircraft one of the faster-growing sources of CO2 emissions in the U.S. transportation sector over the past decade. This trend is likely to be affected, at least temporarily, by reduced air travel in 2020 and 2021 due to Coronavirus Disease 2019 (COVID-19).
The effects of aircraft emissions on the atmosphere are complex, reflecting differing altitudes, geography, time horizons, and environmental conditions. Research has shown that in addition to CO2 emissions, other factors increase the climate change impacts of aviation. These factors include the contribution of aircraft emissions to ozone production; the formation of water condensation trails and cirrus clouds; the emission of various gases and particles, including water vapor, nitrous oxides, sulfates, and particulates from jet fuel combustion; and the high altitude location of the bulk of these emissions. In examining the warming and cooling influences of these factors, the United Nations’ Intergovernmental Panel on Climate Change estimated aviation’s total climate change impact could be from two to four times that of its past CO2 emissions alone.
Aside from GHG emissions, aircraft engines emit a number of criteria—or common—pollutants, including nitrogen oxides, carbon monoxide, oxides of sulfur, unburned or partially combusted hydrocarbons (also known as volatile organic compounds [VOCs]), particulates, and other trace compounds. A subset of the VOCs and particulates are considered hazardous air pollutants.”
In case you wanted a visual representation of how this pollution is said to form and impact our health.
As can be seen, the pollution coming from the aviation industry is a fast-growing problem that is impacting our health and environment in numerous ways. While this has been known for decades and solutions have been presented to try and reverse the impact, nothing is ever implemented to fix the problem. Solutions are only useful if they are enacted upon. While Congress gathers reports, there is little action taken in regards to those reports. It is one thing to acknowledge the negative health and environmental impact yet it is another thing entirely to actually shake up the industry by doing something about it. This seems not to be a major concern as these trails have become worse over time, increasingly contributing to erratic weather, disease, and premature death.
For further evidence of the impact that these trails have on our health and environment, we can turn once again to the EPA to provide more detail. In a document from January 11th, 2021, the EPA enacted standards that are supposed to combat greenhouse gas emissions from the aviation industry. In this document are findings from reports they had compiled in 2016 which call out the dangers these trails have on the public health and welfare:
Control of Air Pollution From Airplanes and Airplane Engines: GHG Emission Standards and Test Procedures
“In August 2016, the EPA issued two findings regarding GHG emissions from aircraft engines (the 2016 Findings).[7]First, the EPA found that elevated concentrations of GHGs in the atmosphere endanger the public health and welfare of current and future generations within the meaning of section 231(a)(2)(A) of the CAA. Second, EPA found that emissions of GHGs from certain classes of engines used in certain aircraft are contributing to the air pollution that endangers public health and welfare under CAA section 231(a)(2)(A). Additional details of the 2016 Findings are described in Section III. As a result of the 2016 Findings, CAA sections 231(a)(2)(A) and (3) obligate the EPA to propose and adopt, respectively, GHG standards for these covered aircraft engines.”
III. Summary of the 2016 Findings
“On August 15, 2016,[46] the EPA issued two findings regarding GHG emissions from aircraft engines. First, the EPA found that elevated concentrations of GHGs in the atmosphere endanger the public health and welfare of current and future generations within the meaning of section 231(a)(2)(A) of the CAA. The EPA made this finding specifically with respect to the same six well-mixed GHGs—CO2, methane, N2 O, hydrofluorocarbons, perfluorocarbons, and sulfur hexafluoride—that together were defined as the air pollution in the 2009 Endangerment Finding [47] under section 202(a) of the CAA and that together were found to constitute the primary cause of climate change. Second, the EPA found that emissions of those six well-mixed GHGs from certain classes of engines used in certain aircraft [48] cause or contribute to the air pollution—the aggregate group of the same six GHGs—that endangers public health and welfare under CAA section 231(a)(2)(A).”
In February of 2022, the EPA proposed standards that would reflect the importance of the control of PM emissions in aviation. They were looking to secure the highest practicable degree of uniformity in aviation regulations and standards. Within this proposal, the EPA provided plenty of insight into the potential health impacts of PM2.5 on human health such as cardiovascular disease, respiratory disease, neurological disorders, asthma, cancer, ferility/reproductive problems, and premature death. They also outlined the impact the chemicals in the trails have on the environment such as affecting the metabolic processes of plant foliage, altering the soil biogeochemistry and microbiology, disrupting plant and animal growth and reproduction, and the corrosion of metals and soil. They even provided more detail on the make-up of the composition of the dangerous toxins inside these trails with the addition of carcinogens such as benzene, 1,3-butadiene, formaldehyde, acetaldehyde, acrolein, polycyclic organic matter (POM), and certain metals such as chromium, manganese, and nickel. Judging by this information alone, it should be rather clear that these trails are negatively impacting our health and environment in numerous ways:
Control of Air Pollution From Aircraft Engines: Emission Standards and Test Procedures
III. Particulate Matter Impacts on Air Quality and Health
A. Background on Particulate Matter
“Particulate matter (PM) is a highly complex mixture of solid particles and liquid droplets distributed among numerous atmospheric gases which interact with solid and liquid phases. Particles range in size from those smaller than 1 nanometer (10−9 meter) to over 100 micrometers (μm, or 10−6 meter) in diameter (for reference, a typical strand of human hair is 70 μm in diameter and a grain of salt is about 100 μm). Atmospheric particles can be grouped into several classes according to their aerodynamic and physical sizes. Generally, the three broad classes of particles include ultrafine particles (UFPs, generally considered as particulates with a diameter less than or equal to 0.1 μm (typically based on physical size, thermal diffusivity or electrical mobility)), “fine” particles (PM2.5; particles with a nominal mean aerodynamic diameter less than or equal to 2.5 μm), and “thoracic” particles (PM10; particles with a nominal mean aerodynamic diameter less than or equal to 10 μm). Particles that fall within the size range between PM2.5 and PM10, are referred to as “thoracic coarse particles” (PM10-2.5, particles with a nominal mean aerodynamic diameter less than or equal to 10 μm and greater than 2.5 μm).
Particles span many sizes and shapes and may consist of hundreds of different chemicals. Particles are emitted directly from sources and are also formed through atmospheric chemical reactions between PM precursors; the former are often referred to as “primary” particles, and the latter as “secondary” particles. Particle concentration and composition varies by time of year and location, and, in addition to differences in source emissions, is affected by several weather-related factors, such as temperature, clouds, humidity, and wind. Ambient levels of PM are also impacted by particles’ ability to shift between solid/liquid and gaseous phases, which is influenced by concentration, meteorology, and especially temperature.
Fine particles are produced primarily by combustion processes and by transformations of gaseous emissions ( e.g., sulfur oxides (SOX), nitrogen oxides (NOX) and volatile organic compounds (VOCs)) in the atmosphere. The chemical and physical properties of PM2.5 may vary greatly with time, region, meteorology, and source category. Thus, PM2.5 may include a complex mixture of different components including sulfates, nitrates, organic compounds, elemental carbon, and metal compounds. These particles can remain in the atmosphere for days to weeks and travel through the atmosphere hundreds to thousands of kilometers.
Particulate matter is comprised of both volatile and non-volatile PM. PM emitted from the engine is known as non-volatile PM (nvPM), and PM formed from transformation of an engine’s gaseous emissions are defined as volatile PM.[35] Because of the difficulty in measuring volatile PM, which is formed in the engine’s exhaust plume and is significantly influenced by ambient conditions, the EPA is proposing standards only for the emission of nvPM.
B. Health Effects of Particulate Matter
Scientific studies show exposure to ambient PM is associated with a broad range of health effects. These health effects are discussed in detail in the Integrated Science Assessment for Particulate Matter (PM ISA), which was finalized in December 2019.[36]The PM ISA concludes that human exposures to ambient PM2.5 are associated with a number of adverse health effects and characterizes the weight of evidence for broad health categories ( e.g., cardiovascular effects, respiratory effects, etc.).[37] The PM ISA additionally notes that stratified analyses ( i.e., analyses that directly compare PM-related health effects across groups) provide strong evidence for racial and ethnic differences in PM2.5 exposures and in PM2.5 -related health risk. As described in Section III.D, concentrations of PM increase with proximity to an airport. Further, studies described in Section III.G report that many communities in close proximity to airports are disproportionately represented by people of color and low-income populations.
EPA has concluded that recent evidence in combination with evidence evaluated in the 2009 p.m. ISA supports a “causal relationship” between both long- and short-term exposures to PM2.5 and mortality and cardiovascular effects and a “likely to be causal relationship” between long- and short-term PM2.5 exposures and respiratory effects.[38]Additionally, recent experimental and epidemiologic studies provide evidence supporting a “likely to be causal relationship” between long-term PM2.5 exposure and nervous system effects, and long-term PM2.5 exposure and cancer. In addition, EPA noted that there was more limited and uncertain evidence for long-term PM2.5 exposure and reproductive and developmental effects ( i.e., male/female reproduction and fertility; pregnancy and birth outcomes), long- and short-term exposures and metabolic effects, and short-term exposure and nervous system effects resulting in the ISA concluding “suggestive of, but not sufficient to infer, a causal relationship.”
More detailed information on the health effects of PM can be found in a memorandum to the docket.[39]
C. Environmental Effects of Particulate Matter
Environmental effects that can result from particulate matter emissions include visibility degradation, plant and ecosystem effects, deposition effects, and materials damage and soiling. These effects are briefly summarized here and discussed in more detail in the memo to the docket cited above.
PM2.5 emissions also adversely impact visibility.[40]In the Clean Air Act Amendments of 1977, Congress recognized visibility’s value to society by establishing a national goal to protect national parks and wilderness areas from visibility impairment caused by manmade pollution.[41] In 1999, EPA finalized the regional haze program (64 FR 35714) to protect the visibility in Mandatory Class I Federal areas. There are 156 national parks, forests and wilderness areas categorized as Mandatory Class I Federal areas (62 FR 38680-38681, July 18, 1997). These areas are defined in CAA section 162 as those national parks exceeding 6,000 acres, wilderness areas and memorial parks exceeding 5,000 acres, and all international parks which were in existence on August 7, 1977. EPA has also concluded that PM2.5 causes adverse effects on visibility in other areas that are not targeted by the Regional Haze Rule, such as urban areas, depending on PM2.5 concentrations and other factors such as dry chemical composition and relative humidity ( i.e., an indicator of the water composition of the particles). EPA established the secondary 24-hour PM2.5 NAAQS in 1997 and has retained the standard in subsequent reviews.[42] This standard is expected to provide protection against visibility effects through attainment of the existing secondary standards for PM2.5 . EPA is reconsidering the 2020 decision, as announced on June 10, 2021.[43]
1. Deposition of Metallic and Organic Constituents of PM
Several significant ecological effects are associated with deposition of chemical constituents of ambient PM such as metals and organics.[44]Like all internal combustion engines, turbine engines covered by this rule may emit trace amounts of metals due to fuel contamination or engine wear. Ecological effects of PM include direct effects to metabolic processes of plant foliage; contribution to total metal loading resulting in alteration of soil biogeochemistry and microbiology, plant and animal growth and reproduction; and contribution to total organics loading resulting in bioaccumulation and biomagnification.
2. Materials Damage and Soiling
Deposition of PM is associated with both physical damage (materials damage effects) and impaired aesthetic qualities (soiling effects). Wet and dry deposition of PM can physically affect materials, adding to the effects of natural weathering processes, by potentially promoting or accelerating the corrosion of metals, by degrading paints and by deteriorating building materials such as stone, concrete and marble.[45]
D. Near-Source Impacts on Air Quality and Public Health
Airport activity can adversely impact air quality in the vicinity of airports. Furthermore, these adverse impacts may disproportionately impact sensitive subpopulations. A recent study by Yim et al. (2015) assessed global, regional, and local health impacts of civil aviation emissions, using modeling tools that address environmental impacts at different spatial scales.[46] The study attributed approximately 16,000 premature deaths per year globally to global aviation emissions, with 87 percent attributable to PM2.5 . The study concludes that about a third of these mortalities are attributable to PM2.5 exposures within 20 kilometers of an airport. Another study focused on the continental United States estimated 210 deaths per year attributable to PM2.5 from aircraft.[47] While there are considerable uncertainties associated with such estimates, these results suggest that in addition to the contributions of PM2.5 emissions to regional air quality, impacts on public health of these emissions in the vicinity of airports are an important public health concern.
A significant body of research has addressed pollutant levels and potential health effects in the vicinity of airports. Much of this research was synthesized in a 2015 report published by the Airport Cooperative Research Program (ACRP), conducted by the Transportation Research Board.[48]The report concluded that PM2.5 concentrations in and around airports vary considerably, ranging from “relatively low levels to those that are close to the NAAQS, and in some cases, exceeding the standards.” [49]
Furthermore, the report states (p. 40) that “existing studies indicate that ultrafine particle concentrations are highly elevated at an airport ( i.e., near a runway) with particle counts that can be orders of magnitude higher than background with some persistence many meters downwind ( e.g., 600 m). Finally, the report concludes that PM2.5 dominates overall health risks posed by airport emissions. Moreover, one recently published study concluded that emissions from aircraft play an etiologic role in pre-term births, independent of noise and traffic-related air pollution exposures.[50]
Since the publication of the 2015 ACRP literature review, a number of studies conducted in the U. S. have been published which concluded that ultrafine particle number concentrations were elevated downwind of commercial airports, and that proximity to an airport also increased particle number concentrations within residences.Hudda et al. investigated ultrafine particle number concentrations (PNC) inside and outside 16 residences in the Boston metropolitan area. They found elevated outdoor PNC within several kilometers of the airport. They also found that aviation-related PNC infiltrated indoors and resulted in significantly higher indoor PNC.[51] In another study in the vicinity of Logan airport, Hudda et al. analyzed PNC impacts of aviation activities.[52] They found that, at sites 4.0 and 7.3 km from the airport, average PNCs were 2 and 1.33-fold higher, respectively, when winds were from the direction of the airport compared to other directions, indicating that aviation impacts on PNC extend many kilometers downwind of Logan airport. Stacey (2019) conducted a literature survey and concluded that the literature consistently reports that particle numbers close to airports are significantly higher than locations distant and upwind of airports, and that the particle size distribution is different from traditional road traffic, with more extremely fine particles.[53] Similar findings have been published from European studies.[54 55 56 57 58 59 ] Results of a monitoring study of communities near Seattle-Tacoma International Airport also found higher levels of ultrafine PM near the airport, and an impacted area larger than at near-roadway sites.[60] The PM associated with aircraft landing activity was also smaller in size, with lower black carbon concentrations than near-roadway samples. As discussed above, PM2.5 exposures are associated with a number of serious, adverse health effects. Further, the PM attributable to aircraft emissions has been associated with potential adverse health impacts.[61 62] For example, He et al. (2018) found that particle composition, size distribution and internalized amount of particles near airports all contributed to promotion of reactive organic species in bronchial epithelial cells.
Because of these potential impacts, a systematic literature review was recently conducted to identify peer-reviewed literature on air quality near commercial airports and assess the quality of the studies.[63] The systematic review identified seventy studies for evaluation. These studies consistently showed that particulate matter, in the form of ultrafine PM (UFP), is elevated in and around airports. Furthermore, many studies showed elevated levels of black carbon, criteria pollutants, and polycyclic aromatic hydrocarbons as well. Finally, the systematic review, while not focused on health effects, identified a limited number of references reporting adverse health effects impacts, including increased rates of premature death, pre-term births, decreased lung function, oxidative DNA damage and childhood leukemia. More research is needed linking particle size distributions to specific airport activities, and proximity to airports, characterizing relationships between different pollutants, evaluating long-term impacts, and improving our understanding of health effects.
A systematic review of health effects associated with exposure to jet engine emissions in the vicinity of airports was also recently published.[64] This study concluded that literature on health effects was sparse, but jet engine emissions have physicochemical properties similar to diesel exhaust particles, and that exposure to jet engine emissions is associated with similar adverse health effects as exposure to diesel exhaust particles and other traffic emissions.A 2010 systematic review by the Health Effects Institute (HEI) concluded that evidence was sufficient to support a causal relationship between exposure to traffic-related air pollution and exacerbation of asthma among children, and suggestive of a causal relationship for childhood asthma, non-asthma respiratory symptoms, impaired lung function and cardiovascular mortality.[65]”
F. Other Pollutants Emitted by Aircraft
“In addition to particulate matter, a number of other criteria pollutants are emitted by the aircraft which are the subject of this proposed rule. These pollutants, which are not covered by the rule, include nitrogen oxides (NOX), including nitrogen dioxide (NO2), volatile organic compounds (VOC), carbon monoxide (CO), and sulfur dioxide (SO2). Aircraft also contribute to ambient levels of hazardous air pollutants (HAP), compounds that are known or suspected human or animal carcinogens, or that have noncancer health effects. These compounds include, but are not limited to, benzene, 1,3-butadiene, formaldehyde, acetaldehyde, acrolein, polycyclic organic matter (POM), and certain metals. Some POM and HAP metals are components of PM2.5 mass measured in turbine engine aircraft emissions.[70]
The term polycyclic organic matter (POM) defines a broad class of compounds that includes the polycyclic aromatic hydrocarbon compounds (PAHs). POM compounds are formed primarily from combustion and are present in the atmosphere in gas and particulate form. Metal compounds emitted from aircraft turbine engine combustion include chromium, manganese, and nickel. Several POM compounds, as well as hexavalent chromium, manganese compounds and nickel compounds are included in the National Air Toxics Assessment, based on potential carcinogenic risk.[71] In addition, as mentioned previously, deposition of metallic compounds can have ecological effects. Impacts of POM and metals are further discussed in the memorandum to the docket referenced above.”
PM stands for particulate matter – the term for a mixture of solid particles and liquid droplets found in the air
Some particles, such as dust, dirt, soot, or smoke, are large or dark enough to be seen with the naked eye while others are too small to be seen
PM10: inhalable particles, with diameters that are generally 10 micrometers and smaller
PM2.5: fine inhalable particles, with diameters that are generally 2.5 micrometers and smaller
These particles come in many sizes and shapes and can be made up of hundreds of different chemicals
Most particles form in the atmosphere as a result of complex reactions of chemicals such as sulfur dioxide and nitrogen oxides
Particulate matter contains microscopic solids or liquid droplets that are so small that they can be inhaled and cause serious health problems
Some particles less than 10 micrometers in diameter can get deep into your lungs and some may even get into your bloodstream
Fine particles are also the main cause of reduced visibility (haze) in parts of the United States
The size of particles is directly linked to their potential for causing health problems
Exposure to such particles can affect both your lungs and your heart
Numerous scientific studies have linked particle pollution exposure to a variety of problems, including:
Premature death in people with heart or lung disease
Nonfatal heart attacks
Irregular heartbeat
Aggravated asthma
Decreased lung function
Increased respiratory symptoms, such as irritation of the airways, coughing or difficulty breathing
People with heart or lung diseases,children, and older adults are the most likely to be affected by particle pollution exposure
According to a Congressional Research Service report from February 8th, 2022, CO2 emissions from aviation are currently experiencing a faster rate of growth than other sources
All aircraft, including military, commercial, and privately chartered, accounted for 13% of the U.S. transportation sector’s CO2 emissions and 5% of all U.S. CO2 emissions in 2018
Commercial aircraft, including those operated by passenger and all-cargo airlines, accounted for 11% of transportation sector and 4% of all emissions
Since the global financial crisis in 2009, aggregate CO2 emissions from all aircraft types have grown steadily, increasing by almost 22% between 2009 and 2018
This increase makes aircraft one of the faster-growing sources of CO2 emissions in the U.S. transportation sector over the past decade
The effects of aircraft emissions on the atmosphere are complex, reflecting differing altitudes, geography, time horizons, and environmental conditions
Research has shown that in addition to CO2 emissions, other factors increase the climate change impacts of aviation which include:
The contribution of aircraft emissions to ozone production
The formation of water condensation trails and cirrus clouds
The emission of various gases and particles, including water vapor, nitrous oxides, sulfates, and particulates from jet fuel combustion
The high altitude location of the bulk of these emissions
In examining the warming and cooling influences of these factors, the United Nations’ Intergovernmental Panel on Climate Change estimated aviation’s total climate change impact could be from two to four times that of its past CO2 emissions alone
Aside from GHG emissions, aircraft engines emit a number of criteria—or common—pollutants, including:
Nitrogen oxides
Carbon monoxide
Oxides of sulfur
Unburned or partially combusted hydrocarbons (also known as volatile organic compounds [VOCs])
Particulates
Other trace compounds
A subset of the VOCs and particulates are considered hazardous air pollutants
According to a 2021 report by the EPA, they found that elevated concentrations of GHGs in the atmosphere endanger the public health and welfare of current and future generations within the meaning of section 231(a)(2)(A) of the CAA
Second, EPA found that emissions of GHGs from certain classes of engines used in certain aircraft are contributing to the air pollution that endangers public health and welfare under CAA section 231(a)(2)(A)
The EPA made this finding specifically with respect to the same six well-mixed GHGs—CO2, methane, N2O, hydrofluorocarbons, perfluorocarbons, and sulfur hexafluoride—that together were defined as the air pollution in the 2009 Endangerment Finding under section 202(a) of the CAA and that together were found to constitute the primary cause of climate change
The EPA found that emissions of those six well-mixed GHGs from certain classes of engines used in certain aircraft cause or contribute to the air pollution—the aggregate group of the same six GHGs—that endangers public health and welfare under CAA section 231(a)(2)(A)
Another report by the EPA from February 2022 states that particulate matter (PM) is a highly complex mixture of solid particles and liquid droplets distributed among numerous atmospheric gases which interact with solid and liquid phases
Particles span many sizes and shapes and may consist of hundreds of different chemicals
Fine particles are produced primarily by combustion processes and by transformations of gaseous emissions (e.g., sulfur oxides (SOX), nitrogen oxides (NOX) and volatile organic compounds (VOCs)) in the atmosphere
PM2.5 may include a complex mixture of different components including sulfates, nitrates, organic compounds, elemental carbon, and metal compounds
These particles can remain in the atmosphere for days to weeks and travel through the atmosphere hundreds to thousands of kilometers
Particulate matter is comprised of both volatile and non-volatile PM
PM emitted from the engine is known as non-volatile PM (nvPM), and PM formed from transformation of an engine’s gaseous emissions are defined as volatile PM
Because of the difficulty in measuring volatile PM, which is formed in the engine’s exhaust plume and is significantly influenced by ambient conditions, the EPA is proposing standards only for the emission of nvPM
In other words, there are no standards proposed by the EPA for the transformation these chemicals go through after leaving the enginewhen they become lingering trails
Scientific studies show exposure to ambient PM isassociated with a broad range of health effects
The PM ISA concludes that human exposures to ambient PM2.5 are associated with a number of adverse health effects and characterizes the weight of evidence for broad health categories ( e.g., cardiovascular effects, respiratory effects, etc.)
EPA has concluded that recent evidence in combination with evidence evaluated in the 2009 p.m. ISA supports a “causal relationship” between both long- and short-term exposures to PM2.5 and mortality and cardiovascular effects and a “likely to be causal relationship” between long- and short-term PM2.5 exposures and respiratory effects
Additionally, recent experimental and epidemiologic studies provide evidence supporting a “likely to be causal relationship” between long-term PM2.5 exposure and nervous system effects, and long-term PM2.5 exposure and cancer
In addition, EPA noted that there was more limited and uncertain evidence for long-term PM2.5 exposure and reproductive and developmental effects ( i.e., male/female reproduction and fertility; pregnancy and birth outcomes), long- and short-term exposures and metabolic effects, and short-term exposure and nervous system effects resulting in the ISA concluding “suggestive of, but not sufficient to infer, a causal relationship”
Environmental effects that can result from particulate matter emissions include:
Visibility degradation
Plant and ecosystem effects
Deposition effects
Materials damage and soiling
PM2.5 emissions also adversely impact visibility
Like all internal combustion engines, turbine engines covered by this rule may emittrace amounts of metals due to fuel contamination or engine wear
Ecological effects of PM include:
Direct effects to metabolic processes of plant foliage
Contribution to total metal loading resulting in alteration of soil biogeochemistry and microbiology, plant and animal growth and reproduction
Contribution to total organics loading resulting in bioaccumulation and biomagnification
Deposition of PM is associated with both physical damage (materials damage effects) and impaired aesthetic qualities (soiling effects)
Wet and dry deposition of PM can physically affect materials, adding to the effects of natural weathering processes, by potentially promoting or accelerating the corrosion of metals, by degrading paints and by deteriorating building materials such as stone, concrete and marble
A recent study by Yim et al. (2015) assessed global, regional, and local health impacts of civil aviation emissions, using modeling tools that address environmental impacts at different spatial scales
The study attributed approximately 16,000 premature deaths per year globally to global aviation emissions, with 87 percent attributable to PM2.5
The study concluded that about a third of these mortalities are attributable to PM2.5 exposures within 20 kilometers of an airport
Another study focused on the continental United States estimated 210 deaths per year attributable to PM2.5 from aircraft
Impacts on public health of these emissions in the vicinity of airports are an important public health concern
A 2015 report concluded that PM2.5 concentrations in and around airports vary considerably, ranging from “relatively low levels to those that are close to the NAAQS, and in some cases, exceeding the standards.”
Furthermore, the report stated (p. 40) that “existing studies indicate that ultrafine particle concentrations are highly elevated at an airport ( i.e., near a runway) with particle counts that can be orders of magnitude higher than background with some persistence many meters downwind ( e.g., 600 m)
Finally, the report concluded that PM2.5 dominates overall health risks posed by airport emissions
Hudda et al. investigated ultrafine particle number concentrations (PNC) inside and outside 16 residences in the Boston metropolitan area and found that aviation-related PNC infiltrated indoors and resulted in significantly higher indoor PNC
Stacey (2019) conducted a literature survey and concluded that the literature consistently reports that particle numbers close to airports are significantly higher than locations distant and upwind of airports, and that the particle size distribution is different from traditional road traffic, with more extremely fine particles
PM2.5 exposures are associated with a number of serious, adverse health effects and the PM attributable to aircraft emissions has been associated with potential adverse health impacts
He et al. (2018) found that particle composition, size distribution and internalized amount of particles near airports all contributed to promotion of reactive organic species in bronchial epithelial cells
A systematic review of 70 studies consistently showed that particulate matter, in the form of ultrafine PM (UFP), is elevated in and around airports
Furthermore, many studies showed elevated levels of black carbon, criteria pollutants, and polycyclic aromatic hydrocarbons as well
Finally, the systematic review, while not focused on health effects, identified a limited number of references reporting adverse health effects impacts, including increased rates of premature death, pre-term births, decreased lung function, oxidative DNA damage and childhood leukemia
A systematic review of health effects associated with exposure to jet engine emissions in the vicinity of airports found that jet engine emissions have physicochemical properties similar to diesel exhaust particles, and that exposure to jet engine emissions is associated with similar adverse health effects as exposure to diesel exhaust particles and other traffic emissions
A 2010 systematic review by the Health Effects Institute (HEI) concluded that evidence was sufficient to support a causal relationship between exposure to traffic-related air pollution and exacerbation of asthma among children, and suggestive of a causal relationship for childhood asthma, non-asthma respiratory symptoms, impaired lung function and cardiovascular mortality
Besides PM2.5, other harmful pollutants, which are not covered by the rule, include:
Nitrogen oxides (NOX)
Nitrogen dioxide (NO2)
Volatile organic compounds (VOC)
Carbon monoxide (CO)
Sulfur dioxide (SO2)
Aircraft also contribute to ambient levels of hazardous air pollutants (HAP), compounds that are known or suspected human or animal carcinogens, or that have noncancer health effects
These compounds include, but are not limited to:
Benzene,
1,3-butadiene
Formaldehyde
Acetaldehyde
Acrolein
Polycyclic organic matter (POM)
Certain metals
Some POM and HAP metals are components of PM2.5 mass measured in turbine engine aircraft emissions
The term polycyclic organic matter (POM) defines a broad class of compounds that includes the polycyclic aromatic hydrocarbon compounds (PAHs)
Metal compounds emitted from aircraft turbine engine combustion include:
Chromium
Manganese
Nickel
Several POM compounds, as well as hexavalent chromium, manganese compounds and nickel compounds are included in the National Air Toxics Assessment, based on potential carcinogenic risk
When dealing with a potential health threat, we tend to jump to the conclusion that we are facing a new “virus” as this well-orchestrated lie has been drilled into our collective consciousness since birth. It is second nature to blame the new invisible boogeyman while overlooking the old visible threats that have been plaguing us for years with no end in sight. It seems too easy to admit to ourselves that any perceived increase in respiratory disease could be attributable to the continued increase in air pollution.
Yet from the start, “Covid-19” has been linked to air pollution. The areas hit the hardest were those with the highest levels of these harmful toxins in the air. As travel died down during the lockdowns, cases fell along with subsiding smog. As travel and pollution rose up again, so too did the “Covid” cases. Even small increases in air pollution has been shown to have an impact on “Covid” case numbers and deaths.
We know for a fact that air pollution is harmful to our health and environment. We know that every single symptom of disease associated with “Covid-19” can be linked to the PM2.5 particles which make up the majority of the dirty air we breathe. We know for a fact that automobiles, factories, power plants, forest fires, volcanic eruptions, etc. all contribute to the harmful levels of toxins in the air. However, the one thing we have been told not to question as a contributor to our current problems are the lingering trails in the sky which form artificial clouds blocking out the beneficial rays of the sun. We are told that these are just regular old contrails from commercial airliners made up of ice crystals which eventually dissipate into a completely safe and harmless nothingness. Anyone questioning the trails is immediately labelled a conspiracy theorist.
It should be clear now, whether you call them chemtrails or not, that these persistent streaks in the sky are full of dangerous substances that attack the cardiovascular, respiratory, and neurological systems. Thanks to government sources such as the EPA and the Congressional Research Service, we know that these trails are the fastest growing pollutant in the air and that they are contributing to even greater levels of smog and haze. The trails and the artificial cirrus clouds they form are a near constant sight in the sky these days and the problem is only growing worse with time. The damaging effects that these lines in the sky have on our health and environment is not even debatable. It is agreed upon by both sides of the debate. That these “persistent contrails” are harmful to our health and environment is a FACT. That the chemicals and toxins found within the vapors cause the exact same symptoms of disease as “Covid-19” is not a coincidence.
Thus we are left with two choices. We can either believe the official narrative that a new “virus” of unknown origin magically leapt from animal to man or somehow escaped from a lab and infected millions of people with a disease that causes the exact same symptoms associated with allergies, the common cold, the flu, and pneumonia. And with it’s rise, it has eliminated the majority of the cases of those previous ailments and can also constantly mutate (over 10 million versions now according to GISAID.org) in order to slip by every possible measure to contain it including masks, social distancing, lockdowns, quarantines, vaccines, etc.
Or we can believe that the ever-increasing and constant daily exposure to air pollution has taken a toll on the populace damaging the health and environment of everyone living within these dangerous levels of toxic fumes. While this is not the only explanation for any perceived increase in respiratory and other diseases, it is the most logical one over an invisible “virus.” According to Occam’s Razor, the simplest of competing theories should be preferred over those that are more complex and that explanations of unknown phenomena should be sought first in terms of known quantities. We know air pollution is harmful. We know that these trails are increasing at a faster rate than any other pollutant. We know that the chemicals residing within them are associated with the exact same symptoms of disease that are ascribed to “Covid.” Unlike a “virus,” we can see this boogeyman with our own two eyes.
All we have to do is look up.
From their own sources, the trails are a threat to our health and our environment. Contrary to what they want you to believe about “persistent contrails,” a.k.a. chemtrails, this is NOT a conspiracy.
You can see more of the slides from Government sources that were presented within this article here.
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Good day South Africa. My name is Ricardo Marmaan and today is the 8th of April 2022, exactly three days after the Western Cape High Court dismissed our ‘Show us the virus‘ court case application, an application for an urgent interim interdict against the lockdown regulations.
It was dismissed with a punitive cost order against me. This judgment came after a 2-month long delay and exactly one day after Ramaphosa made his speech in which he so-called ended the lockdown. We know he did not end it; he merely escalated it by deceptive means.
This is a very strange coincidence. May be no coincidence all.
We asked the Western Cape High Court to grant the people legal protection against being forced by Ramaphosa and the big businesses into these harmful lockdown regulations — like the wearing of the suffocating masks, the use of these poisonous hand sanitizers, and to be forced into taking these deadly vaccinations.
Ramaphosa and these vaccine producers and big businesses already enjoy such legal protection because they are protected by the regulations. They are acting under the regulations.
We asked the Western Cape High Court, in a reasonable and just application, that the people of South Africa be granted the very selfsame legal protections.
But the court unfortunately dismissed our application with a punitive cost order against me.
South Africa, at the very beginning of this process, we asked Ramaphosa to show us the virus. He failed to do so and, therefore, he is perpetrating a virusless pandemic against the people of South Africa.
Parliament, through its silence, is consenting to Ramaphosa and now the judiciary, through its legal — using its legal power and its judgments and rulings protecting and I’m up also protecting the vaccine producers — are protecting Ramaphosa, protecting the vaccine producers, and protecting the big businesses, and depriving the people of South Africa of the very selfsame legal protection.
South Africa, it is time that we see this for what it is. Our beautiful nation has been completely, or more or less completely subverted.
Subversion means that our beautiful nation has been infiltrated by foreign aggressive actors and their local agents. And they are, through lies and deception, leading us to our own self destruction.
The National Health Act amendments will make this subversive and self destructive measures permanent. But Parliament can stop these amendments. Parliament have taken an oath to represent the interests and protect the interest of the people of South Africa, to represent the people of South Africa, to hold Ramaphosa, the Minister of CoGTA [Co-Operative Governance and Traditional Affairs] , and the Minister of Health accountable.
It is time that we wake Parliament up and instruct them because they are our representatives.
I suggest that you go to the Parliament website, parliament.gov [parliament.gov.za], and find the members of Parliament, identify them, contact them and go to them in droves. They live amongst us.
It is time that we instruct them that we the people of South Africa do not want these amendments because they are subversive and self destructive
— that the members of Parliament have a duty to protect the people of South Africa and to stop Ramaphosa
— that if they fail to obey our lawful instructions then it is clear that they are agents of subversion.
South Africa, do not let them divide you. Wake everyone you know up and let us act together. South Africa, do not let them distract you.
Parliament has the power to stop these amendments and we have the lawful authority to instruct Parliament to do so.
South Africa, let us all act together and let us go to Parliament, to the members of Parliament. Let us phone them, let us email them and let us go to them.
And let us say to them that we the people of South Africa say no to these amendments.
As avian influenza runs through the nation’s poultry flocks, with the current extermination of about 28 million laying hens and turkeys, I can’t help but wonder why we aren’t putting beak masks on the chickens.
If masks are so effective against viruses in the human population, why don’t we just make a chicken mask to stop this virus? Seems like a better fix than exterminating all these animals.
The problem is that Dr. Fauci isn’t in the chicken business. Rats. What a shame. If only he were in charge of chickens, he’d have this thing under control in a day. I think we need to expand his authority to the animals of America so he can take care of them like he’s taken care of the humans of America.
When avian flu broke out in our part of Virginia many years ago, two of the federal veterinarians sent in to exterminate chickens visited me just to chat. The independent visits shared an identical assessment: too many chickens crammed in too tight a space in too small a geographic area. Both said if they mentioned that publicly they would be fired.
Hmmmm, I wonder if decentralization of poultry would be better than centralization. Notice that on one farm, 5.8 million laying hens were destroyed—ON ONE FARM!
It’s all blamed on wildlife. Folks, whenever a culture views wildlife as a liability rather than asset, you know everything is wonky. It’s like blaming babies for drug addiction. Or blaming churches for drunkards. When wildlife is the enemy, something is out of whack in the culture’s thinking.
I don’t trust the tests. I don’t trust the experts. I don’t trust the bureaucrats. Isn’t it amazing that as a culture, we’re fixated on prolonging human life for a week or two with ultra-expensive, painful, and invasive intervention but at the first sign of sniffles in a chicken, the “only” cure, according to the experts, is mass extermination. Perhaps the wrong beings are being exterminated. Just sayin’.
The biggest tragedy is that these government gumshoes will come onto a property, without a warrant and unannounced, demanding to pull blood from pastured chickens. They’ll take that sample to a lab driven by political agendas and industrial paradigms (chickens locked in houses are healthier than chickens roaming on a pasture) to determine positive or negative.
Does this sound like incestuous fraternal collusion shenanigans to you?
In a World First on Maria Zeee Uncensored, Australian Senator Malcolm Roberts exposes the Nanotech found in the COVID-19 Vaccines, declaring this is genocide.
We discuss the incoming Digital Identity and the government’s plan to enslave humanity through their plans for a New World Order.
Dr. Naomi Wolf discusses the war on children and on Western values. Forcing children to wear masks is abusive because new studies show that this prevents them from developing normal facial recognition and the practice has a now-measurable effect on their IQ levels.
With all the new information surfacing from the WarRoom/DailyClout volunteers regarding the formerly secret Pfizer documents, and with attorney Stevan Looney’s new essay on the redacted documents in the secret Pfizer tranche now published on DailyClout.io, it is becoming clear that informed consent before receiving the vaccine was never even possible.
Bombshell: in order to process just the paperwork from the “large number of adverse events” — Pfizer’s own words — Pfizer had to hire 2,400 new, full-time employees and the company proudly informed the FDA of these thousands of new hires to grapple with the flood of adverse events they saw as early as February 28, 2021. Yet they did not disclose these adverse events to the public and neither did the FDA.
“The only way that the gain of function/bioweapon narrative makes any sense is if the original Latin definition for the word “virus” is used to explain what is happening in this research. In Latin, “virus” means “liquid poision” and what virologists are doing is simply creating a liquid poison in a lab using cell cultures. What they are not doing is creating “infectious agents of a small size and simple composition that can multiply only in living cells of animals, plants, or bacteria” which is the modern definition for the word according to the Britannica…
[….]
“What must be realized about the GOF studies and the bioweapon narrative is that these stories are designed to keep people believing in the lies of Germ Theory. This is yet another fear-based tactic utilized by those in power to ensure that the masses are frightened of an invisible enemy that can be unleashed upon the world either accidentally or intentionally at a moments notice.”
virus, infectious agent of small size and simple composition that can multiply only in living cells of animals, plants, or bacteria. The name is from a Latin word meaning “slimy liquid” or “poison.”
I have purposefully stayed away from the whole “SARS-COV-2” as a gain of function/bioweapon disinformation campaign as it is obvious to anyone who has ever read any “virus” paper, there is absolutely zero credible evidence for the existence of “SARS-COV-2” or any of these other invisible entities. At no point has any virologist ever properly purified and isolated the particles assumed to be “viruses” directly from a sick patient and then proven them pathogenic in a natural way. As this is a fact that is even admitted by virologists themselves, it should also be obvious that if they can not find the particles assumed to be “viruses” in nature, they can not tinker around and modify these fictional entities in a lab in order to create some sort of contagious bioweapon.
Somehow, this logic escapes many. Even though some have woken to the truth and accepted that “SARS-COV-2” does not exist in nature, they still believe that it must have been developed in a lab and unleashed upon the world in order to create a new contagious disease which is wrecking havoc on the elderly and immunocompromised. What they fail to realize is that there simply is no new disease and that none of the symptoms associated with “SARS-COV-2” are new, unique, or specific. There is zero proof of transmission and/or contagion beyond highly flawed epidemiological studies. There is no new “virus,” no new disease, and no contagious bioweapon. It is pure fiction based upon faulty cell culture and genomic experiments.
Before diving into the experimental evidence presented for gain of function studies, I figured it would be a good idea to get some background information on what exactly these kinds of studies entail first. From the October 2021 Nature article highlighted below, we learn that the gain of function concept earned widespread recognition in 2012 due to a pair of studies which both looked to tweak an avian influenza “virus” in order to make it transmissable by air between ferrets. Disregarding the contradictory fact that aerosol transmission is supposedly the way an upper respiratory “virus” is supposed to spread, many became concerned that this kind of work may eventually lead to the release of a super “virus” which could result in the next pandemic. These ferret studies were apparently pivotal with bringing virology into the gain of function field, even though it could be easily argued that virology has been performing these kinds of experiments throughout its existence.
The gain of function term refers to any research that improves a pathogen’s abilities to cause disease or spread from host to host. This is done by fiddling with cell culture material in a lab combined with genomic sequencing. They do this either by inserting genetic material into the cell culture or by way of animal models where the animal is said to be genetically altered in some way to be more susceptible to the “viral” material.
The article provides an example where mice were genetically modified to become susceptible to MERS. However, the mice did not become ill upon being challenged with the “virus.” Thus, the researchers resorted to passaging the “virus” between mice, which involved infecting a couple of mice, giving the “virus” two days to take hold, and then killing the mice and grinding up the lung tissue to inject into other mice. They repeated these steps at least 30 times which eventually made some mice sick. This process of culturing toxic material, injecting animals with the concoction, killing them and grinding up their remains, and then injecting this emulsified goop into other animals in an attenpt to make them sick is what GOF is all about. While this horrific process is getting recognized today, these kinds of experiments have been a staple of virology since the very beginning:
The shifting sands of ‘gain-of-function’ research
“The term first gained a wide public audience in 2012, after two groups revealed that they had tweaked an avian influenza virus, using genetic engineering and directed evolution, until it could be transmitted between ferrets2,3. Many people were concerned that publishing the work would be tantamount to providing a recipe for a devastating pandemic, and in the years that followed, research funders, politicians and scientists debated whether such work required stricter oversight, lest someone accidentally or intentionally release a lab-created plague. Researchers around the world voluntarily paused some work, but the issue became particularly politicized in the United States.
US funding agencies, which also support research abroad, later imposed a moratorium on gain-of-function research with pathogens while they worked out new protocols to assess the risks and benefits. But many of the regulatory discussions have taken place out of the public eye.
Now, gain-of-function research is once again centre stage, thanks to SARS-CoV-2 and a divisive debate about where it came from. Most virologists say that the coronavirus probably emerged from repeated contact between humans and animals, potentially in connection with wet markets in Wuhan, China, where the virus was first reported. But a group of scientists and politicians argues that a laboratory origin has not been ruled out. They are demanding investigation of the Wuhan Institute of Virology, where related bat coronaviruses have been extensively studied, to determine whether SARS-CoV-2 could have accidentally leaked from the lab or crossed into humans during collection or storage of samples.”
“The term GOF didn’t have much to do with virology until the past decade. Then, the ferret influenza studies came along. In trying to advise the federal government on the nature of such research, the US National Science Advisory Board for Biosecurity (NSABB) borrowed the term — and it stuck, says Gigi Gronvall,a biosecurity specialist at the Bloomberg School of Public Health at Johns Hopkins University in Baltimore, Maryland. From that usage, it came to mean any research that improves a pathogen’s abilities to cause disease or spread from host to host.
Virologists do regularly fiddle with viral genes to change them, sometimes enhancing virulence or transmissibility, although usually just in animal or cell-culture models. “People do all of these experiments all the time,” says Juliet Morrison, a virologist at the University of California, Riverside. For example, her lab has made mouse viruses that are more harmful to mice than the originals. If only mice are at risk, should it be deemed GOF? And would it be worrying?
The answer is generally no. Morrison’s experiments, and many others like them, pose little threat to humans. GOF research starts to ring alarm bells when it involves dangerous human pathogens, such as those on the US government’s ‘select agents’ list, which includes Ebola virus and the bacteria responsible for anthrax and botulism. Other major concerns are ‘pathogens of pandemic potential’ (PPP) such as influenza viruses and coronaviruses. “For the most part, we’re worried about respiratory viruses because those are the ones that transmit the best,” says Michael Imperiale, a virologist at the University of Michigan Medical School. GOF studies with those viruses are “a really tiny part” of virology, he adds.”
“Animal research — although fraught with its own set of ethical quandaries — allows scientists to study how pathogens work and to test potential treatments, a necessary precursor to trials in people. That’s what Perlman and his collaborators had in mind when they set out to study the coronavirus responsible for Middle East Respiratory Syndrome (MERS-CoV), which emerged as a human pathogen in 2012. They wanted to use mice, but mice can’t catch MERS.
The rodents lack the right version of the protein DPP4, which MERS-CoV uses to gain entry to cells. So, the team altered the mice, giving them a human-like version of the gene for DPP4. The virus could now infect the humanized mice, but there was another problem: even when infected, the mice didn’t get very ill. “Having a model of mild disease isn’t particularly helpful to understand why people get so sick,” says collaborator Paul McCray, a paediatric pulmonologist also at the University of Iowa.
So, the group used a classic technique called ‘passaging’ to enhance virulence. The researchers infected a couple of mice, gave the virus two days to take hold, and then transferred some of the infected lung tissue into another pair of mice. They did this repeatedly — 30 times9. By the end of two months, the virus had evolved to replicate better in mouse cells. In so doing, it made the mice more ill; a high dose was deadly, says McCray. That’s GOF of a sort because the virus became better at causing disease. But adapting a pathogen to one animal in this way often limits its ability to infect others, says Andrew Pekosz, a virologist at the Bloomberg School of Public Health.”
“With all the challenges inherent in GOF studies, why do them? Because, some virologists say, the viruses are constantly mutating on their own, effectively doing GOF experiments at a rate that scientists could never match. “We can either wait for something to arise, and then fight it, or we can anticipate that certain things will arise, and instead we can preemptively build our arsenals,” says Morrison. “That’s where gain-of-function research can come in handy.”
This next source is from 2015. The authors admit that virology is heavily reliant on gain or loss of function studies. They offer an alternative definition for GOF research which is any selection process involving an alteration of genotypes and their resulting phenotypes. Obviously, this definition leans far more into the genomics side of the equation. This is due to the claim that these kinds of studies are used by virologists in order to understand a “viruses” genetic make-up. It is stated that researchers now have advanced molecular technologies, such as reverse genetics, which allow them to produce de novo recombinant “viruses” from cloned cDNA. In other words, they mix genetic material from different sources, poison and/or kill lab animals by injecting them with this toxic soup, and then analyze the resulting mixture using computers so that they can claim that the generated model is a new creation. However, it is admitted that these kinds of mutations happen “naturally” with “viruses” every time a person is infected, thus confirming what we already know: virologists can not sequence the same exact “virus” every time:
Gain-of-Function Research: Background and Alternatives
“The field of virology, and to some extent the broader field of microbiology, widely relies on studies that involve gain or loss of function. In order to understand the role of such studies in virology, Dr. Kanta Subbarao from the Laboratory of Infectious Disease at the National Institute of Allergy and Infectious Diseases (NIAID) at the National Institutes of Health (NIH) gave an overview of the current scientific and technical approaches to the research on pandemic strains of influenza and Severe Acute Respiratory Syndrome (SARS) and Middle East Respiratory Syndrome (MERS) coronaviruses (CoV). As discussed in greater detail later in this chapter, many participants argued that the word choice of “gain-of-function” to describe the limited type of experiments covered by the U.S. deliberative process, particularly when coupled with a pause on even a smaller number of research projects, had generated concern that the policy would affect much broader areas of virology research.
TYPES OF GAIN-OF-FUNCTION (GOF) RESEARCH
Subbarao explained that routine virological methods involve experiments that aim to produce a gain of a desired function, such as higher yields for vaccine strains, but often also lead to loss of function, such as loss of the ability for a virus to replicate well, as a consequence. In other words, any selection process involving an alteration of genotypes and their resulting phenotypes is considered a type of Gain-of-Function (GoF) research, even if the U.S. policy is intended to apply to only a small subset of such work.
Subbarao emphasized that such experiments in virology are fundamental to understanding the biology, ecology, and pathogenesis of viruses and added that much basic knowledge is still lacking for SARS-CoV and MERS-CoV. Subbarao introduced the key questions that virologists ask at all stages of research on the emergence or re-emergence of a virus and specifically adapted these general questions to the three viruses of interest in the symposium (see Box 3-1). To answer these questions, virologists use gain- and loss-of-function experiments to understand the genetic makeup of viruses and the specifics of virus-host interaction. For instance, researchers now have advanced molecular technologies, such as reverse genetics, which allow them to produce de novo recombinant viruses from cloned cDNA, and deep sequencing that are critical for studying how viruses escape the host immune system and antiviral controls. Researchers also use targeted host or viral genome modification using small interfering RNA or the bacterial CRISPR-associated protein-9 nuclease as an editing tool.
During Session 3 of the symposium, Dr. Yoshihiro Kawaoka, from the University of Wisconsin-Madison, classified types of GoF research depending on the outcome of the experiments. The first category, which he called “gain of function research of concern,” includes the generation of viruses with properties that do not exist in nature. The now famous example he gave is the production of H5N1 influenza A viruses that are airborne-transmissible among ferrets, compared to the non-airborne transmissible wild type. The second category deals with the generation of viruses that may be more pathogenic and/or transmissible than the wild type viruses but are still comparable to or less problematic than those existing in nature. Kawaoka argued that the majority of strains studied have low pathogenicity, but mutations found in natural isolates will improve their replication in mammalian cells. Finally, the third category, which is somewhere in between the two first categories, includes the generation of highly pathogenic and/or transmissible viruses in animal models that nevertheless do not appear to be a major public health concern. An example is the high-growth A/PR/8/34 influenza strain found to have increased pathogenicity in mice but not in humans. During the discussion, Dr. Thomas Briese, Columbia University, further described GoF research done in the laboratory as being a “proactive” approach to understand what will eventually happen in nature.”
“Imperiale explained that, with respect to the GoF terminology, whenever researchers are working with RNA viruses, GoF mutations are naturally arising all the time and escape mutants isolated in the laboratory appear “every time someone is infected with influenza.” He also commented that the term GoF was understood a certain way by attendees of this symposium, but when the public hears this term “they can’t make that sort of nuanced distinction that we can make here” so the terminology should be revisited.”
Hopefully the above two sources have shown that GOF studies are nothing more than the exact same cell culture experiments utilizing the exact same genomic sequencing technologies and tricks that virologists have always used. The only difference is that they are combining different culture supernatant and genetic materials together into one in order to create a brand new synthetic computer-generated sequence. At no point in time are any purified/isolated particles ever used in these studies. In fact, there are no EM images of the new “virus” of any kind. It should therefore not be surprising that we can see the exact same pattern of unscientific methods and illogical reasoning in GOF studies as found in any of the original “virus” papers.
Seeing as to how the 2012 avian flu studies brought GOF research to the forefront, it seemed ideal to step into this area a bit more to see what actually transpired. The main study presented as evidence of GOF research was led by a man named Ron Fouchier. If that name sounds familiar, that’s because it should. Fouchier was involved in the 2003 “SARS-COV-1” study which proclaimed the satisfaction of Koch’s Postulates for proving a microorganism causes disease yet it failed miserably by not only not being able to satisfy Koch’s four original Postulates, but also Thomas River’s six revised Postulates made strictly for virology. In other words, it was an epic fail.
In Fouchier’s 2012 avian flu GOF study, he attempted to make the H5N1 “virus” infectious through the air. This was done through a process involving cell culturing combined with genetic engineering as well as passaging the material through numerous ferrets. Sounds familiar to the mice example from before, correct? You also see this same process with the early polio and influenza studies as well as in many other virology papers. The main difference is the genomic narrative and the use of modern technology such as reverse genetics to claim the insertion of specific genes.
Highlights from the below paper provide an overview of what was done during this study. It details how the material was collected from a flu strain in Indonesia, genetically altered in a Petri dish, and then transferred to ferrets in a series of experiments using the “wildtype” strain along with different modified strains. Fouchier and Co. were repeatedly unsuccessful in their endeavors of infecting ferrets until they started passaging the “virus” in the animals by injecting them with the cultured soup, grinding up their lung tissues, and injecting other ferrets in the same manner. They repeated this process 6 times and then changed up the experiment by switching to nasal turbinates for the last 4 passage attempts. The only illness said to be achieved via airborne exposure was a loss of appetite, lethargy, and ruffled fur. Upon sequencing the “viruses,” there were only two amino acid switches shared by all six “viruses.” There were several other mutations, but none that occurred in all six airborne “viruses.” In other words, they could not sequence the same “virus” at any point:
Fouchier study reveals changes enabling airborne spread of H5N1
“A study showing that it takes as few as five mutations to turn the H5N1 avian influenza virus into an airborne spreader in mammals—and that launched a historic debate on scientific accountability and transparency—was released today in Science, spilling the full experimental details that many experts had sought to suppress out of concern that publishing them could lead to the unleashing of a dangerous virus.
In the lengthy report, Ron Fouchier, PhD, of Erasmus Medical Center in the Netherlands and colleagues describe how they used a combination of genetic engineering and serial infection of ferrets to create a mutant H5N1 virus that can spread among ferrets without direct contact.
They say their findings show that H5N1 viruses have the potential to evolve in mammals to gain airborne transmissibility, without having to mix with other flu viruses in intermediate hosts such as pigs, and thus pose a risk of launching a pandemic.”
Indonesian H5N1 strain used
Fouchier’s team started with an H5N1 virus collected in Indonesia and used reverse genetics to introduce mutations that have been shown in previous research to make H5N1 viruses more human-like in how they bind to airway cells or in other ways. Avian flu viruses prefer to bind to alpha2,3-linked sialic acid receptors on cells, whereas human flu viruses prefer alpha2,6-linked receptors. In both humans and ferrets, alpha2,6 receptors are predominant in the upper respiratory tract, while alpha 2,6 receptors are found mainly in the lower respiratory tract.
The amino acid changes the team chose included N182K, Q222L, and G224S, the numbers referring to positions in the virus’s HA protein, the viral surface molecule that attaches to host cells. Q222L and G224S together change the binding preference of H2 and H3 subtype flu viruses, changes that contributed to the 1957 and 1968 flu pandemics, according to the report. And N182K was found in a human H5N1 case.
The scientists created three mutant H5N1 virus strains to launch their experiment: one containing N182K, one with Q222L and G2242, and one with all three changes, the report explains. They then launched their lengthy series of ferret experiments by inoculating groups of six ferrets with one of these three mutants or the wild-type H5N1 virus. Analysis of samples during the 7-day experiment showed that ferrets infected with the wild-type virus shed far more virus than those infected with the mutants.
In a second step, the team used a mutation in a different viral gene, PB2, the polymerase complex protein. The mutation E627K in PB2 is linked to the acquisition by avian flu viruses of the ability to grow in the human respiratory tract, which is cooler than the intestinal tract of birds, where the viruses usually reside, according to the report.
The researchers found that this mutation, when added to two of the HA mutations (Q224L and G224S), did not produce a virus that grew more vigorously in ferrets, and the virus did not spread through the air from infected ferrets to uninfected ones.
The passaging step
Seeing that the this mutant failed to achieve airborne transmission, the researchers decided to “passage” this strain through a series of ferrets in an effort to force it to adapt to the mammalian respiratory tract—the move that Fouchier called “really, really stupid,” according to a report of his initial description of the research at a European meeting last September.
They inoculated one ferret with the three-mutation strain and another with the wild-type virus and took daily samples until they euthanized the animals on day 4 and took tissue samples (nasal turbinates and lungs). Material from the tissue samples was then used to inoculate another pair of ferrets, and this step was carried out six times. For the last four passages, the scientists used nasal-wash samples instead of tissue samples, in an effort to harvest viruses that were secreted from the upper respiratory tract.
The amount of mutant virus found in the nasal turbinate and nose swab samples increased with the number of passages, signaling that the virus was increasing its capacity to grow in the ferret upper airway. In contrast, viral titers in the samples from ferrets infected with the wild-type virus stayed the same.
The next step was to test whether the viruses produced through passaging could achieve airborne transmission. Four ferrets were inoculated with samples of the “passage-10” mutant virus, and two ferrets were inoculated with the passage-10 wild strain. Uninfected ferrets were placed in cages next to the infected ones but not close enough for direct contact.
The ferrets exposed to those with the wild virus remained uninfected, but three of the four ferrets placed near those harboring the mutant virus did get infected, the researchers found. Further, they took a sample from one of the “recipient” ferrets and used it to inoculate another ferret, which then transmitted the virus to two more ferrets that were placed near it.
Thus, a total of six ferrets became infected with the mutant virus via airborne transmission. However, the level of viral shedding indicated the airborne virus didn’t transmit as efficiently as the 2009 H1N1 virus does.
In the course of the airborne transmission experiments, the ferrets showed signs of illness, including lethargy, loss of appetite, and ruffled fur. One of the directly inoculated ferrets died, but all those infected via airborne viruses survived.
When the scientists sequenced the genomes of the viruses that spread through the air, they found only two amino acid switches, both in HA, that occurred in all six viruses: H103Y and T156A. They noted several other mutations, but none that occurred in all six airborne viruses.
“Together, these results suggest that as few as five amino acid substitutions (four in HA and one in PB2) may be sufficient to confer airborne transmission of [highly pathogenic avian flu] H5N1 virus,” the researchers wrote.
In further steps, the researchers inoculated six ferrets with high doses of the airborne-transmissible virus; after 3 days, the ferrets were either dead or “moribund.” “Intratracheal inoculations at such high doses do not represent the natural route of infection and are generally used only to test the ability of viruses to cause pneumonia,” the report notes.”
While the proceeding article did an excellent job of providing the main points from Fouchier’s 2012 GOF study, I wanted to showcase relevant highlights directly from the paper to flesh out the methods used even further. Here you will see that Fouchier’s team claimed that they genetically modified A/H5N1 “virus” by site-directed mutagenesis and subsequent serial passage in ferrets. They used Influenza “virus” A/Indonesia/5/2005 (A/H5N1) which they said was isolated from a human case of HPAI “virus” infection. This was passaged once in embryonated chicken eggs which was followed by a single passage in Madin-Darby Canine Kidney (MDCK) cells. All eight gene segments were amplified by reverse transcription polymerase chain reaction and cloned in a modified version of the bidirectional reverse genetics plasmid pHW2000. They then used the QuickChange multisite-directed mutagenesis kit to introduce the desired amino acid substitutions. Site-directed mutagenesis is a synthetic process utilizing PCR to make artificial changes in a DNA sequence. They then took their synthetically-created cultured soup and experimented on ferrets while manipulating the methods until they achieved the results that they desired.
At no point in the paper was a “virus” of any kind ever purified and isolated. At no point were any electron microscope images of the newly mutated “viruses” ever shown. The only “evidence” of an airborne strain is genomic sequencing data from consensus genomes which did not match up. Fouchier and Co. even admitted that airborne transmission could be tested in a second mammalian model system such as guinea pigs, but even this would still not provide conclusive evidence that transmission among humans would occur. They also stated that the mutations they had identified needed further testing to determine their effect on transmission in other A/H5N1 “virus” lineages, and that further experiments are needed to quantify how they affect “viral” fitness and “virulence” in birds and mammals. In other words, their study only told them that they could create mutated genomes and not that they created more “virulent viruses” that are transmissable by air:
Airborne Transmission of Influenza A/H5N1 Virus Between Ferrets
“Highly pathogenic avian influenza A/H5N1 virus can cause morbidity and mortality in humans but thus farhas not acquired the ability to be transmitted by aerosol or respiratory droplet (“airborne transmission”)between humans. To address the concern that the virus could acquire this ability under natural conditions,we genetically modified A/H5N1 virus by site-directed mutagenesis and subsequent serial passage inferrets. The genetically modified A/H5N1 virus acquired mutations during passage in ferrets, ultimatelybecoming airborne transmissible in ferrets. None of the recipient ferrets died after airborne infection withthe mutant A/H5N1 viruses. Four amino acid substitutions in the host receptor-binding protein hemagglutinin, and one in the polymerase complex protein basic polymerase 2, were consistently present in airborne-transmitted viruses. The transmissible viruses were sensitive to the antiviral drug oseltamivir and reacted well with antisera raised against H5 influenza vaccine strains. Thus, avian A/H5N1 influenza viruses can acquire the capacity for airborne transmission between mammals without recombination in an intermediate host and therefore constitute a risk for human pandemic influenza.
Influenza A viruses have been isolated from many host species, including humans, pigs, horses, dogs, marine mammals, and a wide range of domestic birds, yet wild birds in the orders Anseriformes (ducks, geese, and swans) and Charadriiformes (gulls, terns, and waders) are thought to form the virus reservoir in nature (1). Influenza A viruses belong to the family Orthomyxoviridae; these viruses have an RNA genome consisting of eight gene segments (2, 3). Segments 1 to 3 encode the polymerase proteins: basic polymerase 2 (PB2), basic polymerase 1 (PB1), and acidic polymerase (PA), respectively. These proteins form the RNA-dependent RNA polymerase complex responsible for transcription and replication of the viral genome.”
Since the late 1990s, HPAI A/H5N1 viruses have devastated the poultry industry of numerous countries in the Eastern Hemisphere. To date, A/H5N1 has spread from Asia to Europe, Africa, and the Middle East, resulting in the death of hundreds of millions of domestic birds. In Hong Kong in 1997, the first human deaths directly attributable to avian A/H5N1 virus were recorded (11). Since 2003, more than 600 laboratory-confirmed cases of HPAI A/H5N1 virus infections in humans have been reported from 15 countries (12). Although limited A/H5N1 virus transmission between persons in close contact has been reported, sustained human-to-human transmission of HPAI A/H5N1 virus has not been detected (13–15). Whether this virus may acquire the ability to be transmitted via aerosols or respiratory droplets among mammals, including humans, to trigger a future pandemic is a key question for pandemic preparedness. Although our knowledge of viral traits necessary for host switching and virulence has increased substantially in recent years (16, 17), the factors that determine airborne transmission of influenza viruses among mammals, a trait necessary for a virus to become pandemic, have remained largely unknown (18–21). Therefore, investigations of routes of influenza virus transmission between animals and on the determinants of airborne transmission are high on the influenza research agenda.
The viruses that caused the major pandemics of the past century emerged upon reassortment (that is, genetic mixing) of animal and human influenza viruses (22). However, given that viruses from only four pandemics are available for analyses, we cannot exclude the possibility that a futurepandemic may be triggered by a wholly avian virus without the requirement of reassortment. Several studies have shown that reassortment events between A/H5N1 and seasonal human influenza viruses do not yield viruses that are readily transmitted between ferrets (18–20, 23). In our work, we investigated whether A/H5N1 virus could change its transmissibility characteristics without any requirement for reassortment.
We chose influenza virus A/Indonesia/5/2005 for our study because the incidence of human A/H5N1 virus infections and fatalities in Indonesia remains fairly high (12), and there are concerns that this virus could acquire molecular characteristics that would allow it to become more readily transmissible between humans and initiate a pandemic. Because no reassortants between A/H5N1 viruses and seasonal or pandemic human influenza viruses have been detected in nature and because our goal was to understand the biological properties needed for an influenza virus to become airborne transmissible in mammals, we decided to use the complete A/Indonesia/5/2005 virus that was isolated from a human case of HPAI A/H5N1 infection.
We chose the ferret (Mustela putorius furo) as the animal model for our studies. Ferrets have been used in influenza research since 1933 because they are susceptible to infection with human and avian influenza viruses (24). After infection with human influenza A virus, ferrets develop respiratory disease and lung pathology similar to that observed in humans. Ferrets can also transmit human influenza viruses to other ferrets that serve as sentinels with or without direct contact (fig. S1) (25–27).”
Human-to-human transmission of influenza viruses can occur through direct contact, indirect contact via fomites (contaminated environmental surfaces), and/or airborne transmission via small aerosols or large respiratory droplets. The pandemic and epidemic influenza viruses that have circulated in humans throughout the past century were all transmitted via the airborne route, in contrast to many other respiratory viruses that are exclusively transmitted via contact. There is no exact particle size cut-off at which transmission changes from exclusively large droplets to aerosols. However, it is generally accepted that for infectious particles with a diameter of 5 mm or less, transmission occurs via aerosols. Because we did not measure particle size during our experiments, we will use the term “airborne transmission” throughout this Report.”
“Using a combination of targeted mutagenesis followed by serial virus passage in ferrets, we investigated whether A/H5N1 virus can acquiremutations that would increase the risk of mammalian transmission (34). We have previously shown that several amino acid substitutions in the RBS of the HA surface glycoprotein of A/Indonesia/5/2005 change the binding preference from the avian a-2,3–linked SA receptors to the human a-2,6–linked SA receptors (35). A/Indonesia/5/2005 virus with amino acid substitutions N182K, Q222L/G224S, or N182K/Q222L/G224S (numbers refer to amino acid positions in the mature H5 HA protein; N, Asn; Q, Gln; L, Leu; G, Gly; S, Ser) in HA display attachment patterns similar to those of human viruses to cells of the respiratory tract of ferrets and humans (35). Of these changes, we know that together, Q222L and G224S switch the receptor binding specificity of H2 and H3 subtype influenza viruses, as this switch contributed to the emergence of the 1957 and 1968 pandemics (36). N182K has been found in a human case of A/H5N1 virus infection (37).
Our experimental rationale to obtain transmissible A/H5N1 viruses was to select a mutant A/H5N1 virus with receptor specificity for a-2,6–linked SA shed at high titers from the URT of ferrets. Therefore, we used the QuickChange multisite-directed mutagenesis kit (Agilent Technologies, Amstelveen, the Netherlands) to introduce amino acid substitutions N182K, Q222L/G224S, or N182K/Q222L/G224S in the HA of wild-type (WT) A/Indonesia/5/2005, resulting in A/H5N1HA N182K, A/H5N1HA Q222L,G224S, and A/H5N1HA N182K,Q222L,G224S. Experimental details for experiments 1 to 9 are provided in the supplementary materials (25). For experiment 1, we inoculated these mutant viruses andthe A/H5N1wildtype virus intranasally into groups of six ferrets for each virus (fig. S3). Throat and nasal swabs were collected daily, and virus titerswere determined by end-point dilution in Madin Darby canine kidney (MDCK) cells to quantify virus shedding from the ferret URT. Three animals were euthanized after day 3 to enable tissue sample collection. All remaining animals were euthanized by day 7 when the same tissue samples were taken. Virus titers were determined in the nasal turbinates, trachea, and lungs collected post-mortem from the euthanized ferrets. Throughout the duration of experiment 1, ferrets inoculated intranasally with A/H5N1wildtype virus produced high titers in nose and throat swabs—up to 10 times more than A/H5N1HA Q222L,G224S, which yielded the highest virus titers of all three mutants during the 7-day period (Fig. 1). However, no significant difference was observed between the virus shedding of ferrets inoculated with A/H5N1HA Q222L, G224S or A/H5N1HA N182K during the first 3 days when six animals per group were present. Thus, of the viruses with specificity for a-2,6–linked SA, A/H5N1HA Q222L,G224S yielded the highest virus titers in the ferret URT (Fig. 1).
As described above, amino acid substitution E627K in PB2 is one of the most consistent host-range determinants of influenza viruses (29–31). For experiment 2 (fig. S4), we introduced E627K into the PB2 gene of A/Indonesia/5/2005 by site-directed mutagenesis and produced the recombinant virus A/H5N1HA Q222L,G224S PB2 E627K. The introduction of E627K in PB2 did not significantly affect virus shedding in ferrets, because virus titers in the URT were similar to those seen in A/H5N1HA Q222L,G224S-inoculated animals [up to 1 × 104 50% tissue culture infectious doses (TCID50)] (Mann-Whitney U rank-sum test, P = 0.476) (Fig. 1 and fig. S5). When four naïve ferrets were housed in cages adjacent to those with four inoculated animals to test for airborne transmission as described previously (27), A/H5N1HA Q222L,G224S PB2 E627K was not transmitted (fig. S5).
Because the mutant virus harboring the E627K mutation in PB2 and Q222L and G224S in HA did not transmit in experiment 2, we designed an experiment to force the virus to adaptto replication in the mammalian respiratory tract and to select virus variants by repeated passage (10 passages in total) of the constructedA/H5N1HA Q222L,G224S PB2 E627K virus and A/H5N1wildtype virus in the ferret URT (Fig. 2 and fig. S6). In experiment 3, one ferret was inoculated intranasally with A/H5N1wildtype and one ferret with A/H5N1HA Q222L,G224S PB2 E627K. Throat and nose swabs were collected daily from live animals until 4 days postinoculation (dpi), at which time the animals were euthanized to collect samples from nasal turbinates and lungs. The nasal turbinates were homogenized in 3 ml of virus-transport medium, tissue debris was pelleted by centrifugation, and 0.5 ml of the supernatant was subsequently used to inoculate thenext ferret intranasally (passage 2). This procedure was repeated until passage 6.
From passage 6 onward, in addition to the samples described above, a nasal wash was also collected at 3 dpi. To this end, 1 ml of phosphate-buffered saline (PBS) was delivered dropwise tothe nostrils of the ferrets to induce sneezing. Approximately 200 ml of the “sneeze” was collected in a Petri dish, and PBS was added to a final volume of 2 ml. The nasal-wash samples were used for intranasal inoculation of the ferrets for the subsequent passages 7 through 10. We changed the source of inoculum during the course of theexperiment, because passaging nasal washes may facilitate the selection of viruses that were secreted from the URT. Because influenza viruses mutate rapidly, we anticipated that 10 passages would be sufficient for the virus to adapt to efficient replication in mammals.
Virus titers in the nasal turbinates of ferrets inoculated with A/H5N1wildtype ranged from ~1 × 105 to 1 × 107 TCID50/gram tissue throughout 10 serial passages (Fig. 3A and fig. S7). In ferrets inoculated with A/H5N1HA Q222L,G224S PB2 E627K virus, a moderate increase in virus titers in the nasal turbinates was observed as the passage number increased. These titers ranged from 1 × 104 TCID50/gram tissue at the start of the experiment to 3.2 × 105 to 1 × 106 TCID50/gram tissue in the final passages (Fig. 3A and fig. S7). Notably, virus titers in the nose swabs of animals inoculated with A/H5N1HA Q222L,G224S PB2 E627K also increased during the successive passages, with peak virus shedding of 1 × 105 TCID50 at 2 dpi after 10 passages (Fig. 3B).These data indicate that A/H5N1HA Q222L,G224S PB2 E627K was developing greater capacity to replicate in the ferret URT after repeated passage, with evidence for such adaptation becoming apparent by passage number 4. In contrast, virus titers in the nose swabs of the ferrets collected at 1 to 4 dpi throughout 10 serial passages with A/H5N1wildtype revealed no changes in patterns of virus shedding.
Passaging of influenza viruses in ferrets should result in the natural selection of heterogeneous mixtures of viruses in each animal with a variety of mutations: so-called viral quasi-species (38). The genetic composition of the viral quasi-species present in the nasal washe of ferrets after 10 passages of A/H5N1wildtype and A/H5N1HA Q222L,G224S PB2 E627K was determined by sequence analysis using the 454/Roche GS-FLX sequencing platform (Roche, Woerden, the Netherlands) (tables S1 and S2). The mutations introduced in A/H5N1HA Q222L,G224S PB2 E627K by reverse genetics remained present in the virus population after 10 consecutive passages at a frequency >99.5% (Fig. 4 and table S1). Numerous additional nucleotide substitutions were detected in all viral gene segments of A/H5N1wildtype and A/H5N1HA Q222L,G224S PB2 E627Kafter passaging, except in segment 7 (tables S1 and S2). Of the 30 nucleotide substitutions selected during serial passage, 53% resulted in amino acid substitutions.The only amino acid substitution detected upon repeated passage of both A/H5N1wildtype and A/H5N1HA Q222L,G224S PB2 E627Kwas T156A (T, Thr; A, Ala) in HA. This substitution removes a potential N-linked glycosylation site (Asn-X-Thr/Ser; X, any amino acid) in HA and was detected in 99.6% of the A/H5N1wildtype sequences after 10 passages. T156A was detected in 89% of the A/H5N1HA Q222L,G224S PB2 E627K sequences after 10 passages, and the other 11% of sequences possessed the substitution N154K, which removes the same potential N-linked glycosylation site in HA.
In experiment 4 (see supplementary materials), we investigated whether airborne-transmissible viruses were present in the heterogeneous virus population generated during virus passaging in ferrets (fig. S4). Nasal-wash samples, collected at 3 dpi from ferrets at passage 10, were usedin transmission experiments to test whether airborne-transmissible virus was present in the virus quasi-species. For this purpose, nasal-wash samples were diluted 1:2 in PBS and subsequently used to inoculate six naïve ferrets intranasally: two for passage 10 A/H5N1wildtype and four for passage 10 A/H5N1HA-Q222L,G224S PB2 E627K virus.
The following day, a naïve recipient ferret was placed in a cage adjacent to each inoculated donor ferret. These cages are designed to prevent direct contact between animals but allow airflow from a donor ferret to a neighboring recipient ferret (fig. S1) (27). Although mutations had accumulated in the viral genome after passaging of A/H5N1wildtype in ferrets, we did not detect replicating virus upon inoculation of MDCKcells with swabs collected from naïve recipient ferrets after they were paired with donor ferrets inoculated with passage 10 A/H5N1wildtype virus(Fig. 5, A and B). In contrast, we did detect virus in recipient ferrets paired with those inoculated with passage 10 A/H5N1HA Q222L,G224S PB2 E627Kvirus.Three (F1 to F3) out of four (F1 to F4) naïve recipient ferrets became infected as confirmed by the presence of replicating virus in the collected nasal and throat swabs (Fig. 5, C and D). A throat-swab sample obtained from recipient ferret F2, which contained the highest virus titer among the ferrets in the first transmission experiment, was subsequently used for intranasal inoculation of two additional donor ferrets. Both of these animals, when placed in the transmission cage setup (fig. S1), again transmitted the virus to the recipient ferrets (F5 and F6) (Fig. 6, A and B). Avirus isolate was obtained after inoculation of MDCK cells with a nose swab collected from ferret F5 at 7 dpi. The virus from F5 was inoculated intranasally into two more donor ferrets. One day later, these animals were paired with two recipient ferrets (F7 and F8) in transmission cages, one of which (F7) subsequently became infected (Fig. 6, C and D).
We used conventional Sanger sequencing to determine the consensus genome sequences ofviruses recovered from the six ferrets (F1 to F3 and F5 to F7) that acquired virus via airborne transmission (Fig. 4 and table S3). All six samples still harbored substitutions Q222L, G224S,and E627K that had been introduced by reverse genetics. Surprisingly, only two additional amino acid substitutions, both in HA, were consistently detected in all six airborne-transmissible viruses: (i) H103Y (H, His; Y, Tyr), which forms part of the HA trimer interface, and (ii) T156A, which is proximal but not immediately adjacent to the RBS (fig. S8). Although we observed severalother mutations, their occurrence was not consistent among the airborne viruses, indicating that of the heterogeneous virus populations generated by passaging in ferrets, viruses with different genotypes were transmissible. In addition, a single transmission experiment is not sufficient to select for clonal airborne-transmissible viruses because, for example, the consensus sequence of virus isolated from F6 differed from the sequence of parental virus isolated from F2.
Together, these results suggest that as few as five amino acid substitutions (four in HA and one in PB2) may be sufficient to confer airborne transmission of HPAI A/H5N1 virus between mammals. The airborne-transmissible virus isolate with the least number of amino acid substitutions, compared with the A/H5N1wildtype, was recovered from ferret F5. This virus isolate had a total of nine amino acid substitutions; in addition to the three mutations that we introduced (Q222L and G224S in HA and E627K in PB2), this virus harbored H103Y and T156A in HA, H99Y and I368V (I, Ile; V, Val) in PB1, and R99K (R, Arg) and S345N in NP (table S3). Reverse genetics will be needed to identify which of the five to nine amino acid substitutions in this virus are essential to confer airborne transmission.
During the course of the transmission experiments with the airborne-transmissible viruses, ferrets displayed lethargy, loss of appetite, and ruffled fur after intranasal inoculation. One of eight inoculated animals died upon intranasal inoculation (Table 1). In previously published experiments, ferrets inoculated intranasally with WTA/ Indonesia/5/2005 virus at a dose of 1 × 106 TCID50 showed neurological disease and/or death (39, 40). It should be noted that inoculation of immunologically naïve ferrets with a dose of 1 × 106 TCID50 of A/H5N1 virus and the subsequent course of disease is not representative of the natural situation in humans.Importantly, although the six ferrets that became infected via respiratory droplets or aerosol also displayed lethargy, loss of appetite, and ruffled fur, none of these animals died within the course of the experiment. Moreover, previous infections of humans with seasonal influenza viruses are likely to induce heterosubtypic immunity that would offer some protection against the development of severe disease (41, 42). It has been shown that mice and ferrets previously infected with an A/H3N2 virus are clinically protected against intranasal challenge infection with an A/H5N1 virus (43, 44).
After intratracheal inoculation (experiment 5; fig. S9), six ferrets inoculated with 1 × 106 TCID50 of airborne-transmissible virus F5 in a 3-ml volume of PBS died or were moribund at day 3. Intratracheal inoculations at such high doses do not represent the natural route of infection and are generally used only to test the ability of viruses to cause pneumonia (45), as is done for vaccination-challenge studies. At necropsy, the six ferrets revealed macroscopic lesions affecting 80 to 100% of the lung parenchyma with average virus titers of 7.9 × 106 TCID50/gram lung (fig. S10). These data are similar to those described previously for A/H5N1wildtype in ferrets (Table 1). Thus, although the airborne-transmissible virus is lethal to ferrets upon intratracheal inoculation at high doses, the virus was not lethal after airborne transmission.”
“Although our experiments showed that A/H5N1 virus can acquire a capacity for airborne transmission, the efficiency of this mode remains unclear. Previous data have indicated that the 2009 pandemic A/H1N1 virus transmits efficiently among ferrets and that naïve animals shed high amounts of virus as early as 1 or 2 days after exposure (27). When we compare the A/H5N1 transmission data with that of reference (27), keeping in mind that our experimental design for studying transmission is not quantitative, the data shown in Figs. 5 and 6 suggest that A/H5N1 airborne transmission was less robust, with less and delayed virus shedding compared with pandemic A/H1N1 virus.
Airborne transmission could be tested in a second mammalian model system such as guinea pigs (59), but this would still not provide conclusive evidence that transmission among humans would occur. The mutations we identified need to be tested for their effect on transmission in other A/H5N1 virus lineages (60), and experiments are needed to quantify how they affect viral fitness and virulence in birds and mammals. For pandemic preparedness, antiviral drugs and vaccine candidates against airborne-transmissible virus should be evaluated in depth. Mechanistic studies on the phenotypic traits associated with each of the identified amino acid substitutions should provide insights into the key determinants of airborne virus transmission. Our findings indicate that HPAI A/H5N1 viruses have the potential to evolve directly to transmit by aerosol or respiratory droplets between mammals, without reassortment in any intermediate host, and thus pose a risk of becoming pandemic in humans. Identification of the minimal requirements for virus transmission between mammals may have prognostic and diagnostic value for improving pandemic preparedness (34).”
“Influenza virus A/Indonesia/5/2005 (A/H5N1) was isolated from a human case of HPAI virus infection and passaged once in embryonated chicken eggs followed by a singlepassage in Madin-Darby Canine Kidney (MDCK) cells. All eight gene segments were amplified by reverse transcription polymerase chain reaction and cloned in a modified version of the bidirectional reverse genetics plasmid pHW2000 (63-64). Mutations of interest (N182K, Q222L, G224S in HA and E627K in PB2) were introduced in reverse genetics vectors using the QuikChange multi-site-directed mutagenesis kit (Aligent, Amstelveen, The Netherlands) according to the instructions of the manufacturer. Recombinant viruses were produced upon transfection of 293T cells and virus stocks were propagated and titrated in MDCK cells as described (63).
Cells
MDCK cells were cultured in Eagle’s minimal essential medium (EMEM, Lonza Benelux BV, Breda, the Netherlands) supplemented with 10% fetal calf serum (FCS), 100 IU/ml penicillin, 100 μg/ml streptomycin, 2 mM glutamine, 1.5 mg/ml sodium bicarbonate (Lonza), 10 mM Hepes (Lonza), and non-essential amino acids (MP Biomedicals Europe, Illkirch, France). 293T cells were cultured in Dulbecco modified Eagle’s medium (DMEM, Lonza) supplemented with 10% FCS, 100 IU/ml penicillin, 100 mg/ml streptomycin, 2mM glutamine, 1mM sodium pyruvate, and non-essential amino acids.
Virus titration in MDCK cells
Virus titrations were performed as described previously (27). Briefly, MDCK cells were inoculated with tenfold serial dilutions of virus preparations, homogenized tissues, nose swabs, and throat swabs.Cells were washed with PBS one hour after inoculation and cultured in 200μl of infection media, consisting of EMEM supplemented with 100 U/mlpenicillin, 100 μg/ml streptomycin, 2mM glutamine, 1.5mg/ml sodium bicarbonate, 10mM Hepes, non-essential amino acids, and 20 μg/ml trypsin (Lonza). Three days after inoculation, supernatants of infected cell cultures were tested for agglutinating activity using turkey erythrocytes as an indicator of virus replication in the cells. Infectious virus titers were calculated from four replicates each of the homogenized tissue samples, nose swabs, and throat swabs and for ten replicates of the virus preparations by the method of Spearman-Karber (65).”
The term “Gain of Function” first gained a wide public audience in 2012, after two groups revealed that they had tweaked an avian influenza “virus,” using genetic engineering and directed evolution, until it could be transmitted between ferrets
Most virologists say that the “coronavirus” probably emerged from repeated contact between humans and animals, potentially in connection with wet markets in Wuhan, China, where the “virus” was first reported
However, a group of scientists and politicians argues that a laboratory origin has not been ruled out
The term GOF didn’t have much to do with virology until the past decade when the ferret influenza studies came along
From that usage, it came to mean any research that improves a pathogen’s abilities to cause disease or spread from host to host
Virologists regularly fiddle with “viral” genes to change them, sometimes enhancing virulence or transmissibility, although usually just in animal or cell-culture models
Other major concerns are ‘pathogens of pandemic potential’ (PPP) such as influenza “viruses” and “coronaviruses”
“For the most part, we’re worried about respiratory “viruses” because those are the ones that transmit the best,” says Michael Imperiale, a virologist at the University of Michigan Medical School
He added that GOF studies with those “viruses” are “a really tiny part” of virology
Perlman and his collaborators set out to study the “coronavirus” responsible for Middle East Respiratory Syndrome (MERS-CoV), which emerged as a human pathogen in 2012
They wanted to use mice, but mice can’t catch MERS
The rodents lack the right version of the protein DPP4, which MERS-CoV uses to gain entry to cells and so the team altered the mice, giving them a human-like version of the gene for DPP4
The “virus” could now infect the humanized mice, but there was another problem: even when infected, the mice didn’t get very ill
So, the group used a classic technique called ‘passaging’ to enhance “virulence”
The researchers infected a couple of mice, gave the “virus” two days to take hold, and then transferred some of the infected lung tissue into another pair of mice
They did this repeatedly — 30 times and by the end of two months, the “virus” had evolved to replicate better in mouse cells
In so doing, it made the mice more ill; a high dose was deadly
Some virologists say “viruses” are constantly mutating on their own, effectively doing GOF experiments at a rate that scientists could never match
The field of virology, and to some extent the broader field of microbiology, widely relies on studies that involve gain or loss of function
Any selection process involving an alteration of genotypes and their resulting phenotypes is considered a type of Gain-of-Function (GoF) research
Subbarao emphasized that such experiments in virology are fundamental to understanding the biology, ecology, and pathogenesis of “viruses” and added that much basic knowledge is still lacking for “SARS-CoV” and “MERS-CoV”
Virologists use gain- and loss-of-function experiments to understand the genetic makeup of “viruses” and the specifics of “virus-host” interaction
Researchers now have advanced molecular technologies, such as reverse genetics, which allow them to produce de novo recombinant “viruses” from cloned cDNA (i.e. they are synthetic lab creations)
Researchers also use targeted host or “viral” genome modification using small interfering RNA or the bacterial CRISPR-associated protein-9 nuclease as an editing tool
Dr. Yoshihiro Kawaoka, from the University of Wisconsin-Madison, classified types of GoF research depending on the outcome of the experiments:
The fisrt category is “gain of function research of concern,” includes the generation of “viruses” with properties that do not exist in nature
The now famous example he gave is the production of H5N1 influenza A “viruses” that are airborne-transmissible among ferrets, compared to the non-airborne transmissible wild type
The second category deals with the generation of “viruses” that may be more pathogenic and/or transmissible than the wild type “viruses” but are still comparable to or less problematic than those existing in nature (which is odd considering no “viruses” have been found in nature…)
Kawaoka argued that the majority of strains studied have low pathogenicity, but mutations found in natural isolates (there are no natural isolates) will improve their replication in mammalian cells
The third category, which is somewhere in between the first two categories, includes the generation of highly pathogenic and/or transmissible “viruses” in animal models that nevertheless do not appear to be a major public health concern
An example is the high-growth A/PR/8/34 influenza strain found to have increased pathogenicity in mice but not in humans
Dr. Thomas Briese, Columbia University, further described GoF research done in the laboratory as being a “proactive” approach to understand what will eventually happen in nature
GoF mutations are naturally arising all the time and escape mutants isolated in the laboratory appear “every time someone is infected with influenza.”
In other words, they can never sequence the same “virus” every time so what they do in the lab in GoF studies is no different than how they culture and “isolate viruses” in order to sequence the genomes in the first place
A 2012 study supposedly showed that it takes as few as five mutations to turn the H5N1 avian influenza “virus” into an airborne spreader in mammals—and this launched a historic debate on scientific accountability and transparency
In the lengthy report, Ron Fouchier, PhD, of Erasmus Medical Center in the Netherlands and colleagues describe how they used a combination of genetic engineering and serial infection of ferrets to create a mutant H5N1 “virus” that can spread among ferrets without direct contact
Fouchier’s team started with an H5N1 “virus” collected in Indonesia and used reverse genetics to introduce mutations that have been shown in previous research to make H5N1 “viruses” more human-like in how they bind to airway cells or in other ways
The amino acid changes the team chose included N182K, Q222L, and G224S, the numbers referring to positions in the “virus’s” HA protein, the “viral” surface molecule that attaches to host cells
The scientists created three mutant H5N1 “virus” strains to launch their experiment: one containing N182K, one with Q222L and G2242, and one with all three changes
They then launched their lengthy series of ferret experiments by inoculating groups of six ferrets with one of these three mutants or the wild-type H5N1 “virus”
Analysis of samples during the 7-day experiment showed that ferrets infected with the wild-type “virus” shed far more “virus” than those infected with the mutants
In a second step, the team used a mutation in a different “viral” gene, PB2, the polymerase complex protein
The researchers found that this mutation, when added to two of the HA mutations (Q224L and G224S), did not produce a “virus” that grew more vigorously in ferrets, and the “virus” did not spread through the air from infected ferrets to uninfected ones
Seeing that the this mutant failed to achieve airborne transmission, the researchers decided to “passage” this strain through a series of ferrets in an effort to force it to adapt to the mammalian respiratory tract
This was the move that Fouchier called “really, really stupid” (are we sure he wasn’t referring to the whole study?)
They inoculated one ferret with the three-mutation strain and another with the wild-type “virus” and took daily samples until they euthanized the animals on day 4 and took tissue samples (nasal turbinates and lungs)
Material from the tissue samples was then used to inoculate another pair of ferrets, and this step was carried out six times
For the last four passages, the scientists used nasal-wash samples instead of tissue samples, in an effort to harvest “viruses” that were secreted from the upper respiratory tract
In other words, they completely changed the source material from tissue to nasal secretions more than halfway through the experiment
It was said that the amount of mutant “virus” found in the nasal turbinate and nose swab samples increased with the number of passages while “viral” titers in the samples from ferrets infected with the wild-type “virus” stayed the same
Quick Sidenote From the Supplemtary Materials:
“After inoculation with A/H5N1wildtype, virus titers in the nasal turbinates were variable but high, ranging from 1.6 x 105 to 7.9 x 106 TCID50/gram tissue (panel A), with no further increase observed with repeated passage. After inoculation with A/H5N1HA Q222L,G224S PB2 E627K, virus titers in nasal turbinates averaged 1.6 x 104 in the first three passages, 2.5 x 105 in passage four to seven and 6.3 x 105 TCID50/gram tissue in the last three passages, suggestive of improved replication and virus adaptation. In the lungs, no apparent adaptation was observed for animals inoculated with either virus. Virus titers in lungs were highly variable; presumably it was a matter of chance whether the virus reached the lower airways.”
In other words, the “wildtype virus” titers remained and stayed high while the “mutant virus” started low and elevated throughout passaging yet was still underneath the amount seen in the “wildtype” strain. They also note that finding “virus” in the lungs was a “matter of chance” with either “virus.”
End Quick Sidenote.
The next step was to test whether the “viruses” produced through passaging could achieve airborne transmission so four ferrets were inoculated with samples of the “passage-10” mutant “virus,” and two ferrets were inoculated with the passage-10 wild strain
Uninfected ferrets were placed in cages next to the infected ones but not close enough for direct contact
The ferrets exposed to those with the wild “virus” remained uninfected, but three of the four ferrets placed near those harboring the mutant “virus” did get infected (“infected” meaning they found “viral” RNA)
Thus, a total of six ferrets became “infected” with the mutant “virus” via airborne transmission
However, the level of “viral” shedding indicated the airborne “virus” didn’t transmit as efficiently as the 2009 H1N1 “virus”
In the course of the airborne transmission experiments, the ferrets showed signs of illness, including lethargy, loss of appetite, and ruffled fur (no consideration is given to the fact that the animals were caged, tortured, and experimented on)
One of the directly inoculated ferrets died, but all those infected via airborne “viruses” survived
When the scientists sequenced the genomes of the “viruses” that spread through the air, they found only two amino acid switches, both in HA, that occurred in all six “viruses:” H103Y and T156A
They noted several other mutations, but none that occurred in all six airborne “viruses”
In other words, once again they were unable to sequence the exact same genome in the samples from each ferret
In further steps, the researchers inoculated intratracheallysix ferrets with high doses of the airborne-transmissible “virus;” after 3 days, the ferrets were either dead or “moribund”
They stated: “Intratracheal inoculations at such high doses do not represent the natural route of infection and are generally used only to test the ability of viruses to cause pneumonia”
Highly “pathogenic” avian influenza A/H5N1 “virus” can cause morbidity and mortality in humans but thus far has not acquired the ability to be transmitted by aerosol or respiratory droplet (“airborne transmission”) between humans
To address the concern that the “virus” could acquire this ability under natural conditions, the researchers genetically modified A/H5N1 “virus” by site-directed mutagenesis and subsequent serial passage in ferrets
In other words, in order to test whether the “virus” could mutate naturally, they mutated it synthetically…
The genetically modified A/H5N1 “virus” acquired mutations during passage in ferrets, ultimately becoming airborne transmissible in ferrets (all “viruses” aquire mutations every time they are sequenced as no “viral” genome is ever the same as the original)
None of the recipient ferrets died after airborne infection with the mutant A/H5N1 “viruses”
Wild birds in the orders Anseriformes (ducks, geese, and swans) and Charadriiformes (gulls, terns, and waders) are thought to form the “virus” reservoir in nature
Since 2003, more than 600 laboratory-confirmed cases of HPAI A/H5N1 “virus” infections in humans have been reported from 15 countries
Although limited A/H5N1 “virus” transmission between persons in close contact has been reported, sustained human-to-human transmission of HPAI A/H5N1 “virus” has not been detected
Whether this “virus” may acquire the ability to be transmitted via aerosols or respiratory droplets among mammals, including humans, to trigger a future pandemic is a key question for pandemic preparedness
The factors that determine airborne transmission of influenza “viruses” among mammals, a trait necessary for a “virus” to become pandemic, have remained largely unknown
The “viruses” that caused the major pandemics of the past century emerged upon reassortment (that is, genetic mixing) of animal and human influenza “viruses”
However, given that “viruses” from only four pandemics are available for analyses, they cannot exclude the possibility that a future pandemic may be triggered by a wholly avian “virus” without the requirement of reassortment
No reassortants between A/H5N1 “viruses” and seasonal or pandemic human influenza “viruses” have been detected in nature and their goal was to understand the biological properties needed for an influenza “virus” to become airborne transmissible in mammals
They chose the ferret (Mustela putorius furo) as the animal model for the studies as ferrets have been used in influenza research since 1933 because they are susceptible to infection with human and avian influenza “viruses”
There is no exact particle size cut-off at which transmission changes from exclusively large droplets to aerosols
It is generally accepted that for infectious particles with a diameter of 5 mm or less, transmission occurs via aerosols
The researchers used the QuickChange multisite-directed mutagenesis kit to introduce amino acid substitutions in the HA of wild-type “virus”
For experiment 1, they inoculated these mutant “viruses” and the A/H5N1wildtype “virus” intranasally into groups of six ferrets for each “virus”
Throat and nasal swabs were collected daily, and “virus” titers were determined by end-point dilution in Madin Darby canine kidney (MDCK) cells to quantify “virus” shedding from the ferret URT
When four naïve ferrets were housed in cages adjacent to those with four inoculated animals to test for airborne transmission as described previously, A/H5N1HA Q222L,G224S PB2 E627K was not transmitted
Because the mutant “virus” harboring the E627K mutation in PB2 and Q222L and G224S in HA did not transmit in experiment 2, they designed an experiment to force the “virus” to adapt to replication in the mammalian respiratory tract and to select “virus” variants by repeated passage (10 passages in total) of the constructed A/H5N1HA Q222L,G224S PB2 E627K “virus” and A/H5N1wildtype “virus” in the ferret URT
In experiment 3, one ferret was inoculated intranasally with A/H5N1wildtype and one ferret with A/H5N1HA Q222L,G224S PB2 E627K
Throat and nose swabs were collected daily from live animals until 4 days postinoculation (dpi), at which time the animals were euthanized to collect samples from nasal turbinates and lungs
The nasal turbinates were homogenized in 3 ml of “virus-transport” medium, tissue debris was pelleted by centrifugation, and 0.5 ml of the supernatant was subsequently used to inoculate the next ferret intranasally (passage 2)
This procedure was repeated until passage 6
From passage 6 onward, in addition to the samples described above, a nasal wash was also collected at 3 dpi
To this end, 1 ml of phosphate-buffered saline (PBS) was delivered dropwise to the nostrils of the ferrets to induce sneezing
Approximately 200 ml of the “sneeze” was collected in a Petri dish, and PBS was added to a final volume of 2 ml
The nasal-wash samples were used for intranasal inoculation of the ferrets for the subsequent passages 7 through 10
They changed the source of inoculum during the course of the experiment, because passaging nasal washes may facilitate the selection of “viruses” that were secreted from the URT
Because influenza “viruses” mutate rapidly, they anticipated (i.e.guessed arbitrarily) that 10 passages would be sufficient for the “virus” to adapt to efficient replication in mammals
The genetic composition of the “viral” quasi-species present in the nasal washe of ferrets after 10 passages of A/H5N1wildtype and A/H5N1HA Q222L,G224S PB2 E627K was determined by sequence analysis using the 454/Roche GS-FLX sequencing platform
The mutations introduced in A/H5N1HA Q222L,G224S PB2 E627K by reverse genetics remained present in the “virus” population after 10 consecutive passages at a frequency >99.5%
Numerous additional nucleotide substitutions were detected in all “viral” gene segments of A/H5N1wildtype and A/H5N1HA Q222L,G224S PB2 E627K after passaging, except in segment 7
Of the 30 nucleotide substitutions selected during serial passage, 53% resulted in amino acid substitutions
The only amino acid substitution detected upon repeated passage of both A/H5N1wildtype and A/H5N1HA Q222L,G224S PB2 E627K was T156A
In experiment 4, nasal-wash samples, collected at 3 dpi from ferrets at passage 10, were used in transmission experiments to test whether airborne-transmissible “virus” was present in the “virus” quasi-species
For this purpose, nasal-wash samples were diluted 1:2 in PBS and subsequently used to inoculate six naïve ferrets intranasally
Although mutations had accumulated in the “viral” genome after passaging of A/H5N1wildtype in ferrets, they did not detect replicating “virus” upon inoculation of MDCK cells with swabs collected from naïve recipient ferrets after they were paired with donor ferrets inoculated with passage 10 A/H5N1wildtype “virus”
In contrast, they did detect “virus” in recipient ferrets paired with those inoculated with passage 10 A/H5N1HA Q222L,G224S PB2 E627K “virus”
Three out of four naïve recipient ferrets became “infected” as confirmed by the presence of replicating “virus” in the collected nasal and throat swabs (in other words, they saw CPE in a cell culture and claimed “virus” was present)
A “virus isolate” was obtained after inoculation of MDCK cells with a nose swab collected from ferret F5 at 7 dpi
They used conventional Sanger sequencing to determine the consensus genome sequences of viruses recovered from the six ferrets that acquired “virus” via airborne transmission and all six samples still harbored substitutions Q222L, G224S, and E627K that had been introduced by reverse genetics
In other words, they created consensus sequencing through alignment to reference genomes using computer software and algorithms from unpurified material
They observed several other mutations for which their occurrence was not consistent among the airborne “viruses,” indicating that of the heterogeneous “virus” populations generated by passaging in ferrets, “viruses” with different genotypes were transmissible
In other words, they were unable to sequence the exact same “virus” genome every time…and if that wasn’t clear
In addition, a single transmission experiment is not sufficient to select for clonal airborne-transmissible “viruses” because, for example, the consensus sequence of “virus” isolated from F6 differed from the sequence of parental “virus” isolated from F2
Together, they claim that these results suggest that as few as five amino acid substitutions (four in HA and one in PB2) may be sufficient to confer airborne transmission of HPAI A/H5N1 “virus” between mammals
During the course of the transmission experiments with the airborne-transmissible “viruses,” ferrets displayed lethargy, loss of appetite, and ruffled fur after intranasal inoculation
It should be noted that inoculation of immunologically naïve ferrets with a dose of 1 × 106 TCID50 of A/H5N1 “virus” and the subsequent course of disease is not representative of the natural situation in humans
Importantly, although the six ferrets that became “infected” via respiratory droplets or aerosol also displayed lethargy, loss of appetite, and ruffled fur, none of these animals died within the course of the experiment
After intratracheal (in the throat) inoculation, six ferrets inoculated with 1 × 106 TCID50 of airborne-transmissible “virus” F5 in a 3-ml volume of PBSdied or were moribund at day 3
Intratracheal inoculations at such high doses do not represent the natural route of infection and are generally used only to test the ability of “viruses” to cause pneumonia, as is done for vaccination-challenge studies
Although the airborne-transmissible “virus” is lethal to ferrets upon intratracheal inoculation at high doses, the “virus” was not lethal after airborne transmission
They openly admit that the route of injection and the amount of toxic culture goo injected causes the severity of disease, which does not require the “virus” as an explanation
They state that although experiments showed that A/H5N1 “virus” can acquire a capacity for airborne transmission, the efficiency of this mode remains unclear
They pointed out that their experimental design for studying transmission is not quantitative (i.e. they do not know how much “virus” is required for airborne transmission and assume it occurs via PCR results)
They airborne transmission could be tested in a second mammalian model system such as guinea pigs, but this would still not provide conclusive evidence that transmission among humans would occur
The mutations they identified need to be tested for their effect on transmission in other A/H5N1 “virus” lineages, and experiments are needed to quantify how they affect “viral” fitness and “virulence” in birds and mammals
Their findings indicate that HPAI A/H5N1 “viruses” have the potential to evolve directly to transmit by aerosol or respiratory droplets between mammals, without reassortment in any intermediate host, and thus pose a risk of becoming pandemic in human
Of course, the only place reassortment occurs is in a lab so they never need a host…
Identification of the minimal requirements for “virus” transmission between mammals may have prognostic and diagnostic value for improving pandemic preparedness
Influenza “virus” A/Indonesia/5/2005 (A/H5N1) was isolated from a human case of HPAI “virus” infection and passaged once in embryonated chicken eggs followed by a single passage in Madin-Darby Canine Kidney (MDCK) cells
All eight gene segments were amplified by reverse transcription polymerase chain reaction and cloned in a modified version of the bidirectional reverse genetics plasmid pHW2000
Mutations of interest were introduced in reverse genetics vectors using the QuikChange multi-site-directed mutagenesis kit
Recombinant “viruses” were produced upon transfection of 293T cells and “virus” stocks were propagated and titrated in MDCK cells
MDCK cells (canine) were cultured in Eagle’s minimal essential medium supplemented with:
10% fetal calf serum (FCS)
100 IU/ml penicillin
100 μg/ml streptomycin
2 mM glutamine
1.5 mg/ml sodium bicarbonate
10 mM Hepes
Non-essential amino acids
293T cells (human embryonic kidney) were cultured in Dulbecco modified Eagle’s medium supplemented with:
10% FCS
100 IU/ml penicillin
100 mg/ml streptomycin
2mM glutamine
1mM sodium pyruvate
Non-essential amino acids
For “virus” titrations, MDCK cells were inoculated with tenfold serial dilutions of “virus” preparations, homogenized tissues, nose swabs, and throat swabs
Cells were washed with PBS one hour after inoculation and cultured in 200μl of infection media, consisting of EMEM supplemented with:
100 U/ml penicillin
100 μg/ml streptomycin
2mM glutamine
1.5mg/ml sodium bicarbonate
10mM Hepes
Non-essential amino acids
20 μg/ml trypsin
Three days after inoculation, supernatants of infected cell cultures were tested for agglutinating activity using turkey erythrocytes as an indicator of “virus” replication in the cells
Infectious “virus” titers were calculated from four replicates each of the homogenized tissue samples, nose swabs, and throat swabs and for ten replicates of the “virus” preparations by the method of Spearman-Karber
The only way that the gain of function/bioweapon narrative makes any sense is if the original Latin definition for the word “virus” is used to explain what is happening in this research. In Latin, “virus” means “liquid poision” and what virologists are doing is simply creating a liquid poison in a lab using cell cultures. What they are not doing is creating “infectious agents of a small size and simple composition that can multiply only in living cells of animals, plants, or bacteria” which is the modern definition for the word according to the Britannica. The only way the liquid poison can potentially harm one is through injection. Cell cultured soup is not transmitted through the air nor is it infectious and/or contagious. In other words, GOF studies are not creating “viruses” in the modern sense of the word and can only be considered as such if viewed through the original Latin lens.
What must be realized about the GOF studies and the bioweapon narrative is that these stories are designed to keep people believing in the lies of Germ Theory. This is yet another fear-based tactic utilized by those in power to ensure that the masses are frightened of an invisible enemy that can be unleashed upon the world either accidentally or intentionally at a moments notice. There will be figureheads who appear to be on the side of truth, questioning the natural existence of “SARS-COV-2,” challenging the safety of the vaccines, promoting alternative therapies, etc. who will also continue to push the idea that “viruses” exist and can be manipulated in a lab. These people are the Pied Pipers leading those who are going astray back into the fold. There is no need to create a “virus” bioweapon when all that was needed to control the masses is a PCR test and some well-designed propaganda.
To anyone who may have been taken in by this GOF/Bioweapon narrative, remember that there is no evidence of any purified and isolated “viral” particles ever coming directly from human samples that are then proven pathogenic in a natural way. Virology does not dispute this. If they can not find a “virus” in nature, they can not create one in a lab. That is truly all you need to know.
Are the new jabs already prepped & ready to go?
