CORONA Main Coronavirus thread

Pinecone

Has No Life - Lives on TB
Report from the trenches of Ore-gone:

Our area has now moved to a lower stage of mask mandates. We went into Costco, where there is a new sign saying something about if you've had the vaccine, you can come in without a mask, but if you haven't, the CDC suggests that you still do. (I think it actually begins Friday, but they don't seem to be waiting.) I didn't actually read the sign, as I ignore them now, but DH read the first half before he quit.

Being the upright citizen that I am, and not having been vaccinated, I of course! went in without a mask. No questions from anyone. Now I was raised to be an honest person, but I am also not a fool or a sheep. The most discouraging part was seeing kids still wearing masks and about half of the people were wearing them, of all ages. Supposedly, over 66% of the state have been vaccinated, but this Costco is in a more conservative area and I would expect that number to be lower. But being a more conservative area I would have expected more people to just ditch the mask. Either way, there were way more masks then I had hoped to see. The sheep are scared and compliant. This does not bear well for freedom or independence.
 

Mprepared

Veteran Member
"Vaccine advisors to the CDC are now saying there are a “higher-than-expected” number of cases of heart problems in young adults following Covid vaccination."

:shkr: So they expected heart problems from the vaccine??? Or is it just bad journalism. You just can't tell these days.

They expect us to be OKAY with any vaccine side effect for the good OF ALL. If not willing to die for the vaccine, you are against SCIENCE. LOL. What a world of sheep. Better to be a sheep than one of them when the trumps start sounding and the vials are poured.
 

155 arty

Veteran Member

COLLATERAL DAMAGE: New Study CONFIRMS Trump Was Right – And Fauci, Democrats, Media, Tech Giants, etc. Lied About HCQ and AZM to Damage Trump and MURDERED HUNDREDS OF THOUSANDS in Process

By Jim Hoft
Published June 9, 2021 at 11:35am
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Collateral Damage.

That’s the new definition for the US Coronavirus deaths.

covid-deaths-US-2.jpg


The Gateway Pundit has reported extensively this past year on the effects of hydroxychloroquine in treating the COVID-19 virus.

We knew and reported that Dr. Tony Fauci and the medical elites conspired to ban the use of this very successful drug.

We reported earlier on how Dr. Fauci used bogus studies to disqualify HCQ in treating coronavirus.


We also reported that there is proof that Dr. Fauci and top US medical experts all conspired using obviously false information to disqualify hydroxychloroquine and MILLIONS DIED as a result of their action.

We wrote more about that here.

View attachment 270860

A new study released this June revealed at medRxiv suggests that the use of weight-adjusted Hydroxychloroquine (HCQ) and Azithromycin (AZM) appears to be associated with a more than 100% increase in survival, without a clear correlation with ECG abnormalities.

President Trump called this out back in March 2020.

Trump actually promoted the HCQ and AZM combination one year ago!
trump-azm-and-hcq-march-2020.jpg


But Dr. Fauci, the media, the far left tech giants, and Democrats mocked him and disputed this treatment.

They blocked, censored and ridiculed anyone who promoted this successful treatment.

They blocked, censored and banned Gateway Pundit reports on this successful treatment.

And hundreds of thousands of Americans died.

Collateral damage.
Lots of light poles around ,let's get busy! Metaphorically of course!
 

jward

passin' thru
Indo-Pacific News - Watching the CCP-China Threat
@IndoPac_Info


Trump officials who raised lab leak concerns demand punishment for #China for COVID 'abuses' with a ban on research funding and an international effort to release all their military lab data in scathing report Special Report!
2/ David Asher led State Department probe into origins of COVID-19 last year. Along with four other Trump-era officials, he said China would only come clean on what really happened if it faced a high price.
3/ They called for President Biden to investigate whether the Wuhan lab conducted undeclared biological weapons research. And they said he should end funding for controversial 'gain of function' research.
View: https://twitter.com/IndoPac_Info/status/1402629352517373956?s=20
 

marsh

On TB every waking moment

WATCH – Rep. Gaetz Grills FBI Director On Dr. Yan Whistleblower/COVID Origins.
gaetz
Congressman Matt Gaetz (FL-1) has grilled FBI director Christopher Wray on the origins of the coronavirus and what Wray and his FBI knew as Chinese defector/whistleblower Dr. Yan entered the United States in April 2020.

Dr. Yan – who has published a wealth of evidence about the man-made nature of the COVID-19 virus – risked her life entering the United States under the tutelage of Steve Bannon and other dissident groups in the U.S.

Derided by the corporate media, Dr. Yan interacted with FBI agents as early as possible in an attempt to warn American authorities about the cover-up by the Chinese Communist Party.
Watch as Rep. Gaetz becomes the only U.S. Congressman to boldly stand up for the brave whistleblower:

Watch:

Matt Gaetz Demands Answers on Dr. Yan / COVID origins 5:44 min

^^^^^^^^^^^^^^^
Full hearing

View: https://www.youtube.com/watch?v=0iw59m6qNaw
5:53:17 min

Bureau of Investigation
•Streamed live 6 hours ago


Wake Up America! Podcast


FBI Director Christopher Wray will appear and testify before the House Committee on the Judiciary on Thursday to answer questions about the FBI's mishandling of January 6 threats, hacking and terror in the United States.
 

jward

passin' thru
Agree- but- why metaphorically? Perhaps the single healthiest thing we could do as a society is reintroduce the concept of consequences following actions.. or as someone, sometime once said, what we need is something WITH tears(blood) for a change; nothing costs enough here.

Here near LV KS they used to sometimes use empty elevator shafts- I prefer that to messin' up purrfectly good trees or lamppost, but that may be just a matter of aesthetics

Lots of light poles around ,let's get busy! Metaphorically of course!
 
They called for President Biden to investigate whether the Wuhan lab conducted undeclared biological weapons research. And they said he should end funding for controversial 'gain of function' research.
But, then they’ll just have to develop their bio weapons on their own yen.
 

marsh

On TB every waking moment

Global Pushback Against Tyranny Has Begun
by Dr. Joseph Mercola
June 10, 2021

odysee.com 1:2154 min

STORY AT-A-GLANCE
  • March 20, 2021, on the 1-year anniversary of the first COVID-19 lockdown, people in more than 40 countries took to the streets to peacefully demonstrate against COVID-19 lies and tyrannical measures
  • Mainstream media have near-universally censored any news of this global demonstration. Those that did report it either understated the global nature of the event and its attendance, or misrepresented the intent of this “Worldwide Freedom Day”
  • The intent behind Worldwide Freedom Day was to tell our elected officials and unelected global leaders that we withdraw our consent to unconstitutional overreaches and attempts to strip us of our rights and freedoms, and that we will no longer submit to and cower in fear
  • The PCR test is at the heart of the COVID-19 scam. Without the PCR fraud and the asymptomatic spreader lie, the COVID-19 pandemic would have been a short-lived blip
  • Lies have been able to stand through the implementation of universal censorship of anyone who speaks truth and points out the scientific fallacies that drive the pandemic narrative. With these psychological tools, they manufactured the greatest hoax the world has ever seen
March 20, 2021, on the 1-year anniversary of the first COVID-19 lockdown, people in more than 40 countries took to the streets to peacefully demonstrate against COVID-19 lies and tyrannical measures.

The documentary above, “The Pushback,” details the day the world stood together against government overreach and the destruction of human rights — and why we must unite, every day, and push back.

Chances are, you didn’t hear about this global rallying cry for freedom, as the mainstream media have near-universally censored any news of it. The few that did report it either understated the global nature of the event and its attendance, or misrepresented the intent of this “Worldwide Freedom Day.”

Freedom From Fear
So, just what was the intent behind this global demonstration? In short, to tell our elected officials and unelected global leaders that we withdraw our consent to these unconstitutional overreaches and attempts to strip us of our rights and freedoms, and that we will no longer submit to and cower in fear. As noted in the film, fear and hysteria were carefully nurtured using a false narrative that said:
  • A deadly novel virus is sweeping across the planet
  • No one is immune and there’s no cure
  • Asymptomatic people are major disease vectors, and therefore:
  • We have to shut everything down, isolate everyone and wear masks until the whole world has been vaccinated
And, of course, anyone who challenges this crazy narrative is labeled a danger to society. Every part of this narrative is false and unrealistic. In reality:
  • SARS-CoV-2 poses a high risk to a very limited group of people and a negligible risk to the vast majority
  • Few are susceptible to severe illness or death
  • There are several effective treatments available
  • Asymptomatic people — historically known as healthy people — do not spread the infection
  • Lockdowns and mask mandates did not work and have caused great harm
  • Vulnerable people have been harmed instead of helped
Ground Zero of the False Narrative
March 3, 2020, the World Health Organization tweeted out a comment by WHO director-general Tedros Adhanom Ghebreyesus, which said:
“Globally, about 3.4% of reported COVID-19 cases have died. By comparison, seasonal flu generally kills far fewer than 1% of those infected.”
It makes COVID-19 sound like a serious problem indeed. The problem is that Ghebreyesus compared apples and oranges. He reported the case fatality rate (CFR) of COVID-19, versus the infection fatality rate (IFR) for the flu.

As explained in the film, CFR is the proportion of deaths from a disease compared to the number of people diagnosed (the total number of confirmed cases). The IFR, meanwhile, is the proportion of deaths from a disease compared to the total number of infected individuals, confirmed or suspected.

Since CFR requires the infection to be confirmed through laboratory testing and clinical evaluation, and the total number of infected people can be hard to determine and includes suspected cases, the CFR is always lower than the IFR.

By conflating CFR and IFR in the same sentence, comparing two different sets of statistics, Ghebreyesus grossly overstated the threat of COVID-19. Stanford University researcher John Ioannidis pointed this out in a March 7, 2020, response, in which he said, “Reported case fatality rates, like the official 3.4% rate from the WHO, cause horror — and are meaningless.”

October 14, 2020, Ioannidis published a review of 61 seroprevalence studies1 showing that the IFR for COVID-19 was actually only 0.23% — a far cry from the CFR of 3.4% — and for people under the age of 70, the IFR was just 0.05%. In other words, COVID-19 is actually less deadly than the flu. Many have noted that the IFR for flu is typically only around 0.1%, and even at that, COVID-19 is less deadly for people under the age of 70.

PCR Test Added Fuel to the False Narrative
As noted in the documentary, at this point, there are so many false narratives it’s hard to know where to begin, but a good place is the reverse transcription polymerase chain reaction (RT-PCR) test, as it is at the heart of this scam. If it weren’t for this flawed test, there would be no pandemic to speak of.

The fact is, the PCR test is not designed to be used as a diagnostic tool as it cannot distinguish between inactive viruses and “live” or reproductive ones.2 This is a crucial point, since inactive and reproductive viruses are not interchangeable in terms of infectivity. If you have a nonreproductive virus in your body, you will not get sick and you cannot spread it to others.

What’s more, the test was developed using nothing more than computer modeling of a genetic sequence. No actual viral isolate from a patient was ever used in the development of this test.

November 30, 2020, a team of 22 international scientists published a review3 challenging the scientific paper4 on PCR testing for SARS-CoV-2 written by Christian Drosten, Ph.D., and Victor Corman. The Corman-Drosten paper was quickly accepted by the WHO and the workflow described therein was adopted as the standard across the world.

The 22 scientists demanded the Corman-Drosten paper be retracted due to “fatal errors,”5 one of which is the fact that it was written (and the test itself developed) before any viral isolate was available. All they used was the genetic sequence published online by Chinese scientists in January 2020.

As if that doesn’t make the test unreliable enough, laboratories were instructed to amplify the RNA collected far too many times, resulting in healthy people testing “positive.” The number of amplifications is known as the cycle threshold (CT).

When you get a positive result using a CT of 35 or higher, you’re looking at the equivalent of a single copy of viral DNA. The likelihood of that causing a health problem is minuscule. Yet the WHO,6,7,8 the U.S. Food and Drug Administration and the U.S. Centers for Disease Control and Prevention9 were recommending CTs between 40 and 45, thereby guaranteeing a vast majority of “cases” were in fact false positives.

How the Greatest Hoax in History Was Fashioned
As detailed in the featured film, widespread PCR testing gave the mainstream media the fodder needed to create hysteria. For months on end, every broadcast had a tickertape showing the number of “cases” detected.

Other fear-induction tactics included universal masking and 6-foot social distancing rules, replete with plastic barriers everywhere and signs on every floor telling you where to stand and in which direction to walk.

One of the primary tactics that drove the narrative that masking and social distancing were necessities was the lie that asymptomatic people were spreading the infection. Anyone could be a lethal threat. No one was to be exempted from suspicion.

That old man with a cough? Lethal threat. That muscular jogger, flushed from fresh air and exercise? Lethal threat. That pink-faced precocious 2-year-old? Lethal threat. A fearful public soaked up the propaganda and started verbally and physically attacking non-maskers without regard for logic, reason or science.


Without the PCR fraud and the asymptomatic spreader lie, the COVID-19 pandemic would have been a short-lived blip. The lies were able to stand for one reason and one reason only, and that was the implementation of universal censorship of anyone who spoke the truth and pointed out the scientific fallacies that were driving the pandemic narrative.

With these psychological tools — preceded by a single carefully crafted revision of the definition of “pandemic” a decade ago — they manufactured the greatest hoax the world has ever seen. Indeed, you could say the redefinition of pandemic was what brought us to this precipice in the first place. The WHO’s original definition of a pandemic was:10,11
“… when a new influenza virus appears against which the human population has no immunity, resulting in several, simultaneous epidemics worldwide with enormous numbers of deaths and illness.”
The key portion of that definition is “enormous numbers of deaths and illness.” This definition was changed in the month leading up to the 2009 swine flu pandemic. The change was a simple but substantial one: They merely removed the severity and high mortality criteria, leaving the definition of a pandemic as “a worldwide epidemic of a disease.”12

By removing the criteria of severe illness causing high morbidity, leaving geographically widespread infection as the only criteria for a pandemic, the WHO and technocratic leaders of the world were able to bamboozle the global population into believing we were in mortal danger.

What Works and What Doesn’t
The total discarding of science is perhaps the most perplexing part of this pandemic. We’re told to follow the science, but what they actually mean is that we must do as we’re told, without evidence. As noted in the film, we’ve long known what works and what doesn’t, when it comes to pandemic disease mitigation.

Effective measures include hand-washing and isolating the sick. Everything we’ve been told to do over this past year falls squarely in the “proven ineffective” category, and that includes large scale quarantines, border closures, school closures, social distancing and universal mask use. What’s worse, everything we’ve been told that is necessary to save lives, actually fuels disease.

Part 1 of 2
 

marsh

On TB every waking moment
Part 2 of 2

What Was the Pandemic Really About?
In my best-selling book, “The Truth About COVID-19 — Exposing the Great Reset, Lockdowns, Vaccine Passports and the New Normal,” I detail the backstory of how the COVID-19 pandemic was created and, more importantly, why. If you do not understand the geopolitical landscape we’re in right now, you will struggle to understand why anyone would possibly lie about a virus and create a pandemic out of smoke and mirrors.

In a nutshell, a small but highly organized technocratic elite have used this pandemic as a justification for eroding liberty, freedom and democracy from Day 1, and the reason is because they want to usher in a whole new global system. The global elite refer to this new system as the Great Reset, the Fourth Industrial Revolution and the Build Back Better plan.

Make no mistake, the plan — as laid out in various papers and reports, including s 2010 Rockefeller Foundation report,13 in which they describe their “Lockstep” scenario, which is a coordinated global response to a lethal pandemic, and its 2020 white paper,14 “National COVID-19 Testing Action Plan” — is to use bioterrorism to take control of the world’s resources, wealth and people.

The plan is to use the need for coordinated pandemic response as the justification for permanent surveillance and social controls that hobble personal liberty and freedom of choice.

To learn more about the hidden power structure running this global reorganization toward authoritarian control, see “Bill Gates Wants to Realize Global Vision in His Lifetime,” “The Great Reset and Build Back Better,” “Technocracy and the Great Reset” and “Who Pressed the Great Reset Button?

The Time to Stand for Freedom Is Right NOW
In 2007, Naomi Wolf published “The End of America: Letter of Warning to a Young Patriot,” in which she lays out the 10 steps to tyranny. She’s now warning everyone, everywhere, that we are at Step 10. Once Step 10 locks into place, there’s no going back. It’ll be too dangerous to fight back.

Right now, you might face police brutality or censorship. If that dissuades you from doing your part in standing against the totalitarian dictates right now, in the future, you’ll lose everything.

The good news is the would-be tyrants have not won yet. That said, we have no time to spare.

We have no time to remain idle, hoping it will all just go back to normal on its own. In countries where citizens do not have a Second Amendment right to bear arms, the answer is peaceful mass civil disobedience.

In the U.S., we do have the Second Amendment, which allows citizens to own and bear arms, and the mere possibility of an armed uprising makes it more difficult for a tyrannical government to get their way. That said, peaceful disobedience is the primary strategy in armed countries as well.

We must also rally behind legislation that prevents the alteration of laws that safeguard our freedoms. To that end, Wolf has started the Five Freedoms Campaign, which you can find on her Daily Clout website.

The campaign focuses on creating legislation to preserve key freedoms and prevent emergency laws from infringing on our freedom to assemble, worship, protest and engage in business.

Legislation is also being crafted to open schools, remove mask mandates and eliminate requirements for vaccine passports.

Hope, in the Face of Tyranny
I have no doubt that we will ultimately stop the globalists’ drive toward global tyranny. It’s not going to be easy. It may take years, and it may get far worse before it gets better.

The founders of the U.S. fled repressive societies or were children or grandchildren of those who did. They had to personally reckon with criminalized speech, arbitrary arrests and state sanctioned torture and even murder. The men who signed the Declaration of Independence knew that if they lost the war, they would be executed for treason.

These men and women were radicals, fighting for liberty and personal freedoms. They had a vision of reality that was an absolute slap in the face of what the rest of the world tolerated. They were willing to sacrifice their lives to turn that vision into a reality. Most all of us have forgotten their sacrifices and have capitulated to the carefully constructed narrative to create fear that allows most to give up their claim to freedom.

The Founders trusted us to remember our history and remain ever vigilant, to keep the precious web of liberty and personal freedom that they constructed from evaporating so that there would never be an American tyrant. The creators of the U.S. Constitution understood that the price of liberty was eternal vigilance.
Hopefully, enough people will see through the mainstream fog and see the truth of where we’re headed and how we got here (if you don’t, read “The Truth About COVID-19”), and once you understand who the actual enemy is, you become less fearful and more efficient. You can now help educate others, so that they understand what’s going on, how they’re being deceived and what they’re actually about to give up.

Lastly, there are legal solutions that can help thwart the globalist takeover, technological solutions that can strengthen citizens’ lobbying power, and censor-proof technologies that will allow us to circumvent current Big Tech monopolies. We have to work on all of these fronts but, together, I believe we can resecure freedom for our children and future generations.
 

marsh

On TB every waking moment

Disturbing New Info Emerges On Apparent “Magnetic” Side Effects Happening to Some COVID Vaccinated People

June 10, 2021 (7h ago)
2021.06.10-02.55-revolvernews-60c17f3add764.jpg


Have you heard of the “Magnetic Challenge?”

No, it’s not some wacky teenage TikTok challenge, it’s actually much creepier.

It all started as a rumor involving a microchipping conspiracy theory that involved the COVID-19 vaccine.

It’s no secret that many people are leery about taking the vaccine for a number of reasons, namely because it hasn’t gone through the lengthy trials needed in order to receive FDA approval. However, a lot of folks are also convinced that the COVID-19 vaccine is part of a sinister plot to microchip the masses.

One of those conspiracy theories involves “magnetized proteins.”

Here’s some background:

Back in 2016, researchers at the University of Virginia in Charlottesville genetically engineered a magnetized protein called “Magneto.”

That protein was then placed into a virus and injected into an animal’s brain. The point of the research was to use the “Magneto” portion to manipulate neural activity under the remote influence of magnetic fields.

From The Guardian
…the researchers inserted the Magneto DNA sequence into the genome of a virus, together with the gene encoding green fluorescent protein, and regulatory DNA sequences that cause the construct to be expressed only in specified types of neurons. They then injected the virus into the brains of mice, targeting the entorhinal cortex, and dissected the animals’ brains to identify the cells that emitted green fluorescence. Using microelectrodes, they then showed that applying a magnetic field to the brain slices activated Magneto so that the cells produce nervous impulses.

In one final experiment, the researchers injected Magneto into the striatum of freely behaving mice, a deep brain structure containing dopamine-producing neurons that are involved in reward and motivation, and then placed the animals into an apparatus split into magnetised a non-magnetised sections. Mice expressing Magneto spent far more time in the magnetised areas than mice that did not, because activation of the protein caused the striatal neurons expressing it to release dopamine, so that the mice found being in those areas rewarding. This shows that Magneto can remotely control the firing of neurons deep within the brain, and also control complex behaviors.
Creepy stuff, right?

So, you can imagine what happened when viral videos began appearing online showing magnets “stuck” on people’s arms after they received COVID-19 vaccines.

Watch:

View: https://youtu.be/4WfcXNbIXRU
3:30 min

In this next video, an anti-vaccine nurse demonstrates how the Covid vaccine turned her entire body into one big magnet.

Watch:
View: https://twitter.com/i/status/1402709435311591429
.38 min

After watching a number of those videos, the macabre “Magneto” study suddenly felt like it was hitting close to home for a lot of people.

In addition, it didn’t help people’s suspicions and the flow of conspiracy theories when the “fact-checkers” came barreling out of the gates like bats out of hell in order to quickly “debunk’ the viral magnet videos by regurgitating what sounded like Big Pharma talking points.
Take a look at part of what Snopes had to say about the videos:
The underlying claim was false. Regardless of the brand (such as Pfizer, Moderna, or Johnson & Johnson), no COVID-19 vaccine contains radio-frequency identification chips or other types of magnetic devices as part of a nefarious plan to implant people with technology against their will.
The rest of their fact-checking was hypothetical scenarios they cooked up.

Not exactly a rousing debunking, by most people’s standards.

However, not everyone was sold on the idea of “magnetic microchipping mind-control” — it still seemed so far-fetched to many.

And that’s why what happened next really made matters even more perplexing.

A paper published for the 2020 International Symposium On Wearable Computers discusses the use of Magnetic Biosensors in order to monitor social distancing in an effort to prevent COVID-19.

In short, it’s a wearable magnetic-field sensing system.

Here’s what ACM Digital Library states about the project:
We present a wearable, oscillating magnetic field-based proximity sensing system to monitor social distancing as suggested to prevent COVID 19 spread (being between 1.5 and 2.0m) apart. We evaluate the system both in controlled lab experiments and in a real life large hardware store setting. We demonstrate that, due physical properties of the magnetic field, the system is much more robust than current BT based sensing, in particular being nearly 100% correct when it comes to distinguishing between distances above and below the 2.0m threshold.
Here’s a video from one of the authors of the study:
Watch:

View: https://youtu.be/M2fJpfBjfVI
3:03 min

It’s really quite remarkable how many publications were writing about magnetic biosensors in the immediate run-up to the COVID-19 outbreak.

It makes one wonder if that 2016 “Magneto” research had some definitive impact on how to monitor and manage the COVID-19 virus. And in that case, can you really blame people for being suspicious?

After all, not even the fact-checking whiz kids over at Snopes can explain or fully debunk those viral videos.

At this point I think a fair question would be: Do other vaccines also cause some “magnetic properties” to emerge?

It seems like that would be easy enough for someone to research and test by getting a tetanus shot and seeing if that injection site becomes magnetized.

If that’s the case, these videos wouldn’t amount to anything special or be out of the ordinary. However, if that’s not the case, the American people deserve answers, immediately.
 

marsh

On TB every waking moment

BREAKING: CDC Schedules ‘Emergency Meeting’ On Heart Inflammation Cases In COVID Vaccine Recipients
National File's reporting, falsely labeled "misleading" by Twitter, is once again vindicated by the CDC
Gabriel Keane
by GABRIEL KEANE

June 10, 2021

BREAKING: CDC Schedules ‘Emergency Meeting’ On Heart Inflammation Cases In COVID Vaccine Recipients

The Centers for Disease Control has announced Thursday that it has scheduled an emergency meeting to discuss increasing reports of myocarditis and pericarditis (heart inflammation) in individuals who had recently received the COVID vaccine, specifically the mRNA Pfizer and Moderna COVID vaccines.

The virtual meeting is scheduled for June 18 and will last from 11 a.m. to 5 p.m. Eastern Standard Time. The CDC’s Advisory Committee on Immunization Practices (ACIP) has outlined an agenda for the emergency meeting, which lists several data points uncovered during the investigation previously reported on by National File.

The CDC ACIP notes that 488 total reports of heart inflammation have been received regarding the Pfizer vaccine, and 301 total reports have been received regarding the Moderna vaccine. The median range of time for the onset of symptoms from the vaccines is 2-3 days, and the majority of cases involve males whose average age for inflammation symptoms is 30 years old for the first dose, and 24 years old for the second.

Fifteen of the cases involve patients who are still hospitalized at the time of the report, with three remaining in intensive care units. Of the 270 patients who have been discharged, 49 have an unknown recovery status. The report concludes that “Analysis of VAERS preliminary reports of myocarditis/pericarditis is in progress, including follow-up to obtain medical records, complete reviews, apply CDC working case definition, and adjudicate cases.”

National File’s reporting on the CDC investigation into myocarditis cases in May was falsely labeled as “misleading” by Twitter, despite the facts that the sourcing for the article came directly from the CDC’s website. Users were unable to like or retweet the story, and were cautioned by a message in bold text that partially redirected, ironically, to the CDC’s website.

1623383350933.png

Twitter has not corrected its decision to incorrectly label the story as “misleading,” or provided any explanation for the censorship.
 

marsh

On TB every waking moment

NEW: Passengers on First Fully Vaccinated North American Cruise Test Positive For Covid-19

By Cristina Laila
Published June 10, 2021 at 6:45pm
IMG_2030.jpg

Passengers aboard the first 100% vaccinated North American cruise tested positive for Covid-19.

Two passengers on the Celebrity Millennium, which is operated by Royal Caribbean, tested positive for Covid-19 during end-of-cruise testing which is conducted 72 hours before returning to the US.

The passengers are asymptomatic and have been forced into isolation on the vessel.
WFLA Tampa reported:
Two people on the first cruise setting sail from North America since the pandemic tested positive for COVID-19 at the end of the crew.

All passengers were required to show proof of vaccination in addition to a negative COVID-19 test within a 72-hour period before the ship departed from the Caribbean island of St. Maarten Saturday.

“The buffets are handled very well and instead of the passengers utilizing the utensils and serving themselves, the crew wearing gloves were serving the passengers,” Stewart Chiron, “The Cruise Guy,” said to NewsNation’s Brian Entin.

The vessel is currently docked in Curaço and the passengers who tested positive remain on board in isolation. The ship will return to St. Maarten this Saturday to disembark.
The cruise line released a statement:

“Today two guests sharing a stateroom onboard Celebrity Millennium tested positive for COVID-19 while conducting the required end of cruise testing. The individuals are asymptomatic and currently in isolation and being monitored by our medical team. We are conducting contact tracing, expediting testing for all close contacts and closely monitoring the situation.

“Celebrity Millennium is sailing with fully vaccinated crew and guests and following comprehensive protocols that align with our destination partners and exceed CDC guidelines to protect the health and safety of our guests. All guests on Celebrity Millennium were required to show proof of vaccination as well as a negative COVID-19 test within 72 hours before sailing from St. Maarten this past Saturday. This situation demonstrates that our rigorous health and safety protocols work to protect our crew, guests and the communities we visit.”
 

marsh

On TB every waking moment

15 States Are Moving to Curb Public Health Agency Powers Following Lockdown Carnage

More than a dozen states have passed or advanced legislation to place new checks on the powers of public health agencies in the wake of the pandemic.

Wednesday, June 9, 2021
15-states_curb_public-health-agencies.jpg

Jon Miltimore

Jon Miltimore

Mike Fratantuono grew up in a restaurant. Literally.

For decades, Sunset Restaurant in Glen Burnie, Maryland, was the family business. Over the years, he’d done seemingly every job imaginable: busboy, bartender, and butcher; prep cook and plumber; handyman and manager.

Fratantuono says that’s what made it so hard to watch the family’s legacy become a COVID casualty in 2020.

“It kills me. We were supposed to be getting ready to celebrate our 60th anniversary this year, and instead we’re packing up and closing at the end of this month,” Fratantuono told the Washington Post last year. “I try not to get too sentimental about it, because it won’t change a damn thing, but sometimes the stress hits me and my heart starts going like crazy. I get frustrated. It makes me angry.”

Fratantuono is just one of the countless business owners across America who saw their dreams vanish before their eyes in the wake of government lockdowns that crushed their businesses.

Now, in the wake of the pandemic, states across the country are advancing legislation to curb the powers of public health departments following one of the most destructive and contentious years in American history.

Reining in Public Health Agencies
In May, the Network for Public Health Law published a report showing that in recent months no fewer than 15 state legislatures have passed or are considering passing measures that would restrict the legal authority of public health departments.

Among the provisions passed or considered are the following:
● Prohibitions on requiring citizens to wear masks;
● Prohibiting health agencies from closing businesses or schools;
● Banning the use of quarantines for people who have not been shown to be sick;
● Preventing state hospitals and universities from requiring vaccinations for employees and students;
● Preventing local governments from exercising emergency powers that are inconsistent with state health department guidelines;

Earlier this year, for example, North Dakota passed legislation making it unlawful for state officials to force citizens to wear masks—just one of a growing number of states to place restrictions on mask orders. In March, Kansas’s legislature passed legislation that removes the governor’s ability to shut down businesses during a public health emergency.

Meanwhile, more than 40 states passed legislation that made it unlawful for health departments to mandate COVID-19 vaccination.

A Serious Threat to Life?
The report concludes that opposition to “reasonable” public health measures poses serious dangers to life and health.

“Legislation to stop expert public health agencies from leading the response to health emergencies creates unforeseen, serious risks to life and health,” the report states. “These laws could make it harder to advance health equity during a pandemic that has disproportionately sickened and killed Black, Hispanic and Latino, and Indigenous Americans.”

Not mentioned in the report, however, are the unintended consequences of the actions taken by public health agencies across the country in 2020. The collateral damage of lockdowns included business closures, job losses, supply disruptions, mass protests, surging violence, increased mental health problems, unprecedented drug overdoses, and a collapse in cancer screenings.

Public health agencies, meanwhile, proved incapable of taming the coronavirus through the use of lockdowns. And these struggles were not confined to the United States.

“A new study by German scientists claims to have found evidence that lockdowns may have had little effect on controlling the coronavirus pandemic,” The Telegraph reported last week.

“Statisticians at Munich University found ‘no direct connection’ between the German lockdown and falling infection rates in the country.”

The Lesson of Lockdowns
The devastating impact of lockdowns, combined with their failure to slow the spread of the virus, demonstrates why states are right to curb the powers of public health agencies.

If 2020 taught us anything, it’s the danger of unchecked executive power. Using emergency powers, governors and public health bureaucrats across the country took unilateral, sweeping, and indefinite measures that massively damaged livelihoods and infringed on the rights of millions of Americans. People were fined and arrested for simply gathering privately or exercising outside, walking a pet, paddling a boat on the water (alone), or taking a child to the park—even though most transmissions took place in homes and the coronavirus is rarely transmitted outdoors.

Americans may disagree on the precise role public health departments should play in society today. But the pandemic reminded us why checks and balances on concentrated power are so important.

The American constitutional system was deliberately designed to avoid concentrated power because the Framers feared it above all else.

“The only maxim of a free government ought to be to trust no man living with power to endanger the public liberty,” wrote John Adams.

The authors of the Network for Public Health Law report express concern that public health agencies are being stripped of the power to act by dangerous radicals. The truth is that dangerously radical government agencies are being put in check.

Ohio, for example, passed a law in March that limits the length of a public health emergency order to 90 days unless it’s extended by the legislature. The same month, lawmakers in Utah passed legislation allowing the state legislature to override state health agency orders during public health emergencies. Missouri, meanwhile, has proposed a law that limits lockdowns to 15 days, after which extensions must be approved by legislative bodies.

These reforms are not radical. They are both reasonable and sensible. They do not represent an attack on science—which tells us what is, not what we ought to do—but are prudent checks on power from lawmakers acting within their rightful province.

“It is necessary to curb the power of government,” the economist Ludwig von Mises noted in Human Action. “This is the task of all constitutions, bills of rights and laws. This is the meaning of all struggles which men have fought for liberty.”

The preservation of liberty, protected by separating and checking power, is the ideal on which the American system was founded. Following a year that saw Americans’ rights, dreams, and health trampled by central planners wielding vast power with little restraint and few checks, it’s a vision Americans are right to rekindle.

Just ask Mike Fratantuono and the millions of other Americans whose lives were derailed in 2020.
 

marsh

On TB every waking moment

Too timid? Experts worry pursuing lab-leak theory may upset U.S.-China relations

Antagonizing China, some experts fear, might jeopardize the secretive regime's cooperation in both finding the source of COVID-19, as well as preventing or mitigating future pandemics.

By Daniel Payne
Updated: June 11, 2021 - 2:02pm

A chorus of public health experts and commentators are warning the U.S. to tread carefully in pursuing the COVID-19 lab-leak theory, lest an aggressive investigation worsen already strained U.S.-China relations.

Largely ignored and disparaged by the press and the scientific community over the last 18 months, the lab-leak theory has received an explosion of interest starting several weeks after Joe Biden's inauguration in January. A growing number of scientists, writers and government officials have ramped up pressure to mount a thorough international investigation to determine whether or not the SARS-Cov-2 virus leaked from a Chinese coronavirus lab located in Wuhan just a few miles from the first reported outbreak of the virus.

Adding to the theory's credibility, the Biden administration has itself ordered the U.S. Intelligence Community to investigate the possibility of the lab leak. Yet multiple experts and media figures are cautioning against pursuing the theory too energetically, fearing that such pursuits could further injure the already-weakened relationship between the United States and China.
In a Washington Post op-ed earlier this month, Georgetown University virologist Angela Rasmussen and University of Utah post-doctoral virology lab affiliate Stephen Goldstein argued that the natural theory of the virus was the most credible explanation for its origin. While allowing that doctors should continue to look into the possibility of a lab leak, the scientists said the stronger case rests on looking for animals that may have harbored the virus before the pandemic.

"Getting better answers will take rigorous scientific work — and cooperation from China," they wrote. "As frustrating as obfuscation by the Chinese government is, the answers are there. If we make accusations and demands that aren't firmly grounded in evidence, we run the real risk of having no origins investigations at all."

Rasmussen and Goldstein did not respond to requests for comment on the issue.

In the science journal Nature, meanwhile, writer Amy Maxmen reported on claims that "the volatility of the debate could thwart efforts to study the virus's origins."

Among the experts making that argument is David Fidler, a senior fellow for global health at the Council on Foreign Relations. He told Maxmen that the U.S. is continuing "to poke China in the eye on this issue of an investigation," something that's distracting from the need to "get ready for the next pandemic."

Fidler told Just the News that the "eyeball-to-eyeball politics of the U.S.-China geopolitical rivalry" are obstructing efforts to get the pandemic fully under control.

"What we've got now is a zero-sum contest between the U.S. Intelligence Community and the Chinese Communist Party," he said.

"In order to produce what's needed from a scientific and epidemiology point of view, you can't have an issue of the origins of an outbreak politicized this way," he continued. He acknowledged that China was "the first culprit" in politicizing the pandemic, by attempting to cover up the earliest phase of the outbreak in that country in order to protect its international reputation.

Both countries need to "step up to the plate and begin to build some bilateral communications in order to look ahead," he concluded.

Jennifer Huang Bouey, a researcher with Rand Corp., told Kaiser Health News that the international community should "reduce the political tension and let the scientists do the work, not the politicians."

Denis Simon, an expert in China business and technology strategy at Duke University, told the same news service that there could be "hell to pay" if investigators make confident pronouncements that the virus originated in the Chinese lab.

"We haven't figured out the consequences to the answer," he said. "I'm very concerned about our ability to manage the emotions loosed if that hypothesis were to be accepted."

Michael Hiltzik, a columnist with the L.A. Times who has called the lab-leak theory "fact-free" and who this week underscored the fractured expert consensus on the possibility, argued to Just the News that "we very much need Chinese cooperation to get to the bottom of this" and that a strong U.S. stance on the matter could endanger that cooperation.

Hiltzik said that "marching into a country known for its sensitivity to its geo-political reputation" with a goal to "find a basis to point a finger at them" will likely hamstring efforts to address the larger questions of the pandemic.

As Hiltzik and others have noted, the explosion of interest in the lab-leak theory has not been accompanied by an explosion in new evidence. Most of the attention focused on the theory in recent weeks and months has been from politicians and scientists calling for further investigations into the lab.

Much criticism has been leveled at the World Health Organization's international team investigation into the origins of COVID-19, which consisted of a relatively brief trip to China that included what was apparently just one day's worth of investigations at the Wuhan Institute of Virology talking with lab scientists about their undertakings there.

Fidler said the possibility of a lab leak "has always been plausible."

"We have known for a very long time that laboratory leaks can be a problem and, depending on the pathogen, can seed a serious outbreak, an epidemic or a pandemic," he said. "It's never, from a scientific point of view, been dismissed as impossible."

But the two countries "have some functional things that we have to do," he argued, "something that would break this toxic spiral down into this zero-sum contest that's preventing the two big powers in the world from getting past this particular issue to focus on future worry."
 

marsh

On TB every waking moment

Another 60MM J&J Doses Produced At Troubled Baltimore Plant Are Tainted, FDA Says

FRIDAY, JUN 11, 2021 - 02:00 PM
Readers may remember earlier this year when an accident at the Emergent Biosolutions lab in Baltimore led to millions of J&J and AstraZeneca doses being ruined (after workers cross-contaminated them with ingredients from AstraZeneca jabs being produced in the same factory).

Since the incident, the FDA has been reviewing safety and production procedures at the facility. But despite the US government handing over control to J&J, attempts to re-start production have been in limbo, and according to the NYT, another 60MM doses produced at the facility didn't meet the agency's safety standards.
In a statement, the F.D.A. said that before making its decision, it "conducted a thorough review of facility records and the results of quality testing performed by the manufacturer." It also considered the ongoing public health emergency. The agency said it was continuing to “work through issues” at the Baltimore plant with Johnson & Johnson and Emergent.
Dr. Peter Marks, the F.D.A.’s top vaccine regulator, said in the statement that the agency has been conducting an extensive review of batches of vaccine produced at the plant “while Emergent BioSolutions prepares to resume manufacturing operations with corrective actions to ensure compliance with the F.D.A.’s current good manufacturing practice requirements."
Representatives from Johnson & Johnson and Emergent declined to comment on the agency’s decision.
Fortunately for President Biden, the US already has enough Pfizer and Moderna doses to satisfy domestic demand. But the latest production hiccup will make it more difficult for the US to export doses to countries around the world in desperate need of them.



Of the ruined doses, 10MM will be sold in the US, and abroad with a special warning label that regulators can use for drugs that are in short supply. The warning will read that "regulators cannot guarantee that Emergent BioSolutions, the company that operates the plant, followed good manufacturing practices."
The F.D.A.’s action is disappointing news for Emergent and Johnson & Johnson, which hired the firm as a subcontractor. Inspectors are still reviewing the plant and are not expected to decide whether the company can reopen it until later this month, according to people familiar with the situation. Regulators are also continuing to cast doubt on whether the company, which has been paid hundreds of millions of dollars by the federal government to manufacture coronavirus vaccines, adhered to manufacturing standards.

The agency’s plan to allow 10 million doses to be used in the United States or abroad with a warning is somewhat unusual for a product under emergency authorization, experts said. Regulators have the discretion to take that action if the drugs are badly needed and in short supply, they said.

In a statement, the FDA said that before making its decision, it “conducted a thorough review of facility records and the results of quality testing performed by the manufacturer.” It also considered the ongoing public health emergency. The agency said it was continuing to “work through issues” at the Baltimore plant with Johnson & Johnson and Emergent.
But the real issue here is that after months of scrutiny and interrupted production, the Emergent factory, a key piece of America's vaccine infrastructure, still isn't producing anywhere near full capacity.

The FDA hasn't decided yet whether the factory should be placed back under Emergent's control. So far, doses produced at the factory have played little to no role in the US vaccination program. Most of the J&J doses administered in the US so far were manufactured at the company's plant in the Netherlands. For weeks now, the FDA has been trying to figure out what to do about at least 170MM doses of the vaccine that were left in limbo after the discovery of the production mishap mentioned above.

While the loss of 60MM J&J doses that could have been sold or donated is certainly "a blow" to the Biden Administration's vaccine policy, the White House announced earlier this week that the US had agreed to purchase 500MM more doses from Pfizer and Moderna at cost provided the vaccines are donated to other countries with greater need.
 

marsh

On TB every waking moment

EXCLUSIVE!!! THE LAWSUIT WE’VE BEEN WAITING FOR! Fauci and His COVID-19 Henchmen Sued to Personally Pay For Their Abuses!

ByTimothy Shea
10 June 2021
https://magainstitute.com/the-lawsu...les-sued-to-personally-pay-for-their-abuses/#


FINALLY! The lawsuit we’ve all been waiting for! An exhaustively researched, very tightly reasoned, and persuasively pled complaint condemning the Government’s COVID-19 response was filed today in the United States District Court for the Northern District of Alabama to hold the minute martinet, Anthony “Fluttering Fastball” Fauci and his co-conspirators at DHHS, CDC, NIH, and FDA accountable for their reign of terror over America.

Forty three named and unnamed plaintiffs led by America’s Frontline Doctors have sued Secretary of the U.S. Department of Health and Human Services (DHHS) Xavier Becerra, both personally and in his official capacity, Director of the National Institute of Allergies and Infectious Diseases (NIAID) Dr. Anthony Fauci, both personally and in his official capacity, Acting Commissioner of the Food and Drug Administration (FDA) Dr. Janet Woodcock, both personally and in her official capacity, DHHS itself, FDA itself, the Center for Disease Control and Prevention (CDC), National Institute of Health (NIH), NIAID itself, and John and Jane Does I-V.

The theory of the case is that the EUAs were “the keys that unlocked the profit potential of the COVID-19 crisis,” enabling vaccine manufacturers to “reap billions of dollars in profit by exploiting the fears of the American people.” The complaint further alleges that the vaccines “have the potential to cause substantially greater harm than the SARS-CoV-2 virus and the COVID-19 disease” themselves.
Defendants are seeking civil money damages from Secretary Becarra, Dr. Fauci, and Dr. Woodcock personally.
The Complaint alleges that the Emergency Use Authorizations (EUAs) under which various “unapproved, inadequately tested, experimental, and dangerous” COVID-19 vaccines have been sold and administered are unlawful on multiple grounds and must be terminated immediately. The multiple grounds supporting termination of the EUAs, and by extension, administration of all COVID-19 vaccines, follows.

First, the Complaint alleges that the Emergency Declaration upon which the EUAs are all based was unjustified. Second, that the DHHS Secretary has failed to satisfy the “criteria for issuance” of the EUAs set forth in Section 546 of the Food, Drugs and Cosmetics Act 21 U.S.C. § 360bbb-3(c). Third, that the DHHS Secretary has failed to satisfy the “conditions of authorization” mandated by § 360bbb-3(e)(1)(A). If the District Court finds any of these grounds to be legally sustainable, the EUAs must as a matter of law be terminated.

Plaintiffs Seek Multiple Rulings and Damages From Individual Defendants

The Plaintiffs are asking the District Court to review whether there was a true “public health emergency” and to find that, since there was no such actual emergency, that DHHS did not have the authority to declare such an emergency, which would likewise nullify the EUAs.
the EUAs were “the keys that unlocked the profit potential of the COVID-19 crisis”
The Plaintiffs are also asking the District Court to determine that the EUAs and extensions thereof are unlawful based on the grounds set forth above, that the Defendants have violated customary international law by engaging in non-consensual human medical experimentation, and that they have unlawfully failed to implement protections for human subjects in medical experimentation.

They are further asking the District Court to enjoin the enforcement of the overall “public health emergency” declaration and renewals, enforcement of the EUAs, and extension of the EUAs to children under the age of 16.

Finally, the Defendants are seeking civil money damages from Secretary Becarra, Dr. Fauci, and Dr. Woodcock personally.

The case is Civil Action No. 2:21-cv-00702-CLM. A copy of the complaint follows.
Americas-Frontline-Doctors-v.-Becarra-COMPLAINT-1-FILEDDownload
 

marsh

On TB every waking moment

Exclusive: Vindicated Trump Says Only Lab Leak Question Is If It Was ‘On Purpose’

JUNE 11, 2021 By Ben Weingarten

Former President Donald Trump took a victory lap over the theory that the Chinese coronavirus leaked from the Wuhan Institute of Virology (WIV).

It “came from Wuhan, it came from the lab,” he said in an exclusive interview this week. “I don’t have a question: ‘Did it come from the lab?’ I have a question, ‘Did they do it on purpose, or was it an accident?’”

Most likely, the former president guesses, the virus escaped the Wuhan lab “through gross incompetence, and it got away from them [the Chinese authorities], and they panicked.”

“I don’t think they knew what to do,” he continued. “The one thing they did know to do is to shut it [Wuhan] off from the rest of China,” but not to “shut it [China] off to the outside world.”

Over the last month, a number of prominent scientists and science reporters have argued the so-called lab leak theory is plausible if not probable, challenging peers who spent months disparaging it as a conspiracy theory. Intelligence reported by the Wall Street Journal in May indicated several scientists at the WIV were hospitalized in November 2019, weeks before China’s “patient zero” was identified, fueling speculation about the lab leak theory.

Sudden consideration of the lab leak theory by the corporate media prompted an about-face from the Biden administration, which called for a 90-day intelligence community review of the virus’s origins mere hours after revelations emerged it had quashed a similar effort initiated by the Trump administration.

Despite the Biden administration and the corporate media’s abrupt change of tone, the Wall Street Journal’s recent revelations largely corroborated what the outgoing Trump administration State Department had theorized months earlier. Trump sees the sudden acceptance of the lab leak theory by the same institutions that previously mocked it as intensely political, attributing the original dismissal of the theory to two potential causes.

The first is simply that he endorsed it, and therefore a hostile political and media establishment automatically opposed it. The New York Times’s Maggie Haberman has basically admitted as much.

Second, China has American “politicians … wrapped around their finger,” Trump hypothesized. “China told them to” take an adverse position, he said of the public officials who harangued him over the theory. From the earliest days of the COVID outbreak, the Chinese Communist Party has sought to distance itself from the virus broadly, and the WIV as its point of origin in particular — obfuscation that itself makes the lab leak theory more plausible.

In a recent rally, President Trump called for China to pay at least $10 trillion in restitution for the damage caused by the outbreak, and recommended “all countries should collectively cancel any debt they owe to China as a down payment on reparations.”

China “should pay something for that kind of gross mismanagement, incompetence, or if it were done purposely,” he told me.

Trump’s comments came during an interview conducted for a book project on U.S.-China policy on which I am working thanks to The Fund for American Studies’ Robert Novak Journalism Fellowship.
 

marsh

On TB every waking moment

How Fanatics Took Over The World

FRIDAY, JUN 11, 2021 - 09:40 PM
Authored by Jeffrey Tucker via DailyReckoning.com,

Early in the pandemic, I had been furiously writing articles about lockdowns. My phone rang with a call from a man named Dr. Rajeev Venkayya. He is the head of a vaccine company but introduced himself as former head of pandemic policy for the Gates Foundation.

Now I was listening.

I did not know it then, but I’ve since learned from Michael Lewis’s (mostly terrible) book The Premonition that Venkayya was, in fact, the founding father of lockdowns. While working for George W. Bush’s White House in 2005, he headed a bioterrorism study group. From his perch of influence – serving an apocalyptic president — he was the driving force for a dramatic change in U.S. policy during pandemics.

He literally unleashed hell.

That was 15 years ago. At the time, I wrote about the changes I was witnessing, worrying that new White House guidelines (never voted on by Congress) allowed the government to put Americans in quarantine while closing their schools, businesses, and churches shuttered, all in the name of disease containment.

I never believed it would happen in real life; surely there would be public revolt. Little did I know, we were in for a wild ride…



The Man Who Lit the Match
Last year, Venkayya and I had a 30-minute conversation; actually, it was mostly an argument. He was convinced that lockdown was the only way to deal with a virus. I countered that it was wrecking rights, destroying businesses, and disturbing public health. He said it was our only choice because we had to wait for a vaccine. I spoke about natural immunity, which he called brutal. So on it went.

The more interesting question I had at the time was why this certified Big Shot was wasting his time trying to convince a poor scribbler like me. What possible reason could there be?

The answer, I now realized, is that from February to April 2020, I was one of the few people (along with a team of researchers) who openly and aggressively opposed what was happening.

There was a hint of insecurity and even fear in Venkayya’s voice. He saw the awesome thing he had unleashed all over the world and was anxious to tamp down any hint of opposition. He was trying to silence me. He and others were determined to crush all dissent.

This is how it has been for the better part of the last 15 months, with social media and YouTube deleting videos that dissent from lockdowns. It’s been censorship from the beginning.

For all the problems with Lewis’s book, and there are plenty, he gets this whole backstory right. Bush came to his bioterrorism people and demanded some huge plan to deal with some imagined calamity. When Bush saw the conventional plan — make a threat assessment, distribute therapeutics, work toward a vaccine — he was furious.
“This is bulls**t,” the president yelled.
“We need a whole-of-society plan. What are you going to do about foreign borders? And travel? And commerce?”
Hey, if the president wants a plan, he’ll get a plan.
“We want to use all instruments of national power to confront this threat,” Venkayya reports having told colleagues.
“We were going to invent pandemic planning.”
This was October 2005, the birth of the lockdown idea.

Dr. Venkayya began to fish around for people who could come up with the domestic equivalent of Operation Desert Storm to deal with a new virus. He found no serious epidemiologists to help. They were too smart to buy into it. He eventually bumped into the real lockdown innovator working at Sandia National Laboratories in New Mexico.

Cranks, Computers, and Cooties

His name was Robert Glass, a computer scientist with no medical training, much less knowledge, about viruses. Glass, in turn, was inspired by a science fair project that his 14-year-old daughter was working on.

She theorized (like the cooties game from grade school) that if school kids could space themselves out more or even not be at school at all, they would stop making each other sick. Glass ran with the idea and banged out a model of disease control based on stay-at-home orders, travel restrictions, business closures, and forced human separation.

Crazy right? No one in public health agreed with him but like any classic crank, this convinced Glass even more. I asked myself, “Why didn’t these epidemiologists figure it out?” They didn’t figure it out because they didn’t have tools that were focused on the problem. They had tools to understand the movement of infectious diseases without the purpose of trying to stop them.

Genius, right? Glass imagined himself to be smarter than 100 years of experience in public health. One guy with a fancy computer would solve everything! Well, he managed to convince some people, including another person hanging around the White House named Carter Mecher, who became Glass’s apostle.

Please consider the following quotation from Dr. Mecher in Lewis’s book: “If you got everyone and locked each of them in their own room and didn’t let them talk to anyone, you would not have any disease.”

At last, an intellectual has a plan to abolish disease — and human life as we know it too! As preposterous and terrifying as this is — a whole society not only in jail but solitary confinement — it sums up the whole of Mecher’s view of disease. It’s also completely wrong.

Pathogens are part of our world; they are generated by human contact. We pass them onto each other as the price for civilization, but we also evolved immune systems to deal with them. That’s 9th-grade biology, but Mecher didn’t have a clue.

Fanatics Win the Day

Jump forward to March 12, 2020. Who exercised the major influence over the decision to close schools, even though it was known at that time that SARS-CoV-2 posed almost risk to people under the age of 20? There was even evidence that they did not spread COVID-19 to adults in any serious way.

Didn’t matter. Mecher’s models — developed with Glass and others — kept spitting out a conclusion that shutting down schools would drop virus transmission by 80%. I’ve read his memos from this period — some of them still not public — and what you observe is not science but ideological fanaticism in play.

Based on the timestamp and length of the emails, he was clearly not sleeping much. Essentially he was Lenin on the eve of the Bolshevik Revolution. How did he get his way?

There were three key elements: public fear, media and expert acquiescence, and the baked-in reality that school closures had been part of “pandemic planning” for the better part of 15 years. Essentially, the lockdowners, over the course of 15 years, had worn out the opposition. Lavish funding, attrition of wisdom within public health, and ideological fanaticism prevailed.

Figuring out how our expectations for normal life were so violently foiled, how our happy lives were brutally crushed, will consume serious intellectuals for many years. But at least we now have a first draft of history.

As with almost every revolution in history, a small minority of crazy people with a cause prevailed over the humane rationality of multitudes. When people catch on, the fires of vengeance will burn very hot.

The task now is to rebuild a civilized life that is no longer so fragile as to allow insane people to lay waste to all that humanity has worked so hard to build.
 

marsh

On TB every waking moment

COVID rules that make no sense — and the politicians who refuse to give up control
By David Marcus
June 10, 2021 | 2:26pm | Updated

We were directed that masks must be worn at all times."
Cuomo forces NY school district to keep mask mandate, goes against own health dept

Across America, states are casting off the shackles of COVID restrictions and returning to normal. Not a new normal, not a variation on normal, but plain, good old-fashioned normal.

Meanwhile, absolutely nobody is surprised that New York Gov. Andrew Cuomo’s position is, essentially, “Not so fast.”

You see, here in the Empire State — aptly named as it is still widely ruled through Emperor Cuomo’s emergency powers — our daily lives are still riddled with a hodgepodge of contradictory and oft bizarre restrictions on our freedoms. Like a jilted paramour, Cuomo simply can’t accept that the COVID crisis is over.

The current landscape of COVID regulations enforced by Cuomo’s regime simply makes no sense. Over at the Barclays Center in Brooklyn, more that 10,000 fans, often maskless while eating and drinking, watch the mighty Nets course through the NBA playoffs.

Andrew Cuomo is not prepared to completely reopen NYC.Carlo Allegri-Pool/Getty Images
Meanwhile, across town at Penn Station, recently rebuilt as an airy and open cathedral of transportation, the mask mandates persist. If you are sitting shoulder to shoulder screaming cheers for Kevin Durant, no mask. But if you sit alone on a bench quietly reading while awaiting your train, mask up.

1623479128562.png

Nets fans who root for their team at the Barclays Center in Brooklyn often have their masks off inside the facility.Arturo Holmes/Getty Images

As has been the case from Day 1 of this pandemic, the situation is even worse, more confusing, and more nonsensical for our children. The policies on masking kids at school seem to change every 10 minutes or so for no apparent reason. New York Senate GOP leader Rob Ortt, who is leading the effort to remove King Cuomo’s crown, said he has spoken to school officials “who are utterly angry, who are upset, and who are confused.”

The only justification for these continued restrictions, for not following the lead of places like Texas and Florida where our citizens are flocking, appears to be Cuomo’s own gargantuan ego. He likes parceling out little flecks of freedom to his plebes. One imagines him powder-wigged, with a gentle back-of-the-hand royal wave announcing, “I doth declare upon this day that in accordance with science, masks shall not be worn on Thursdays.”

1623479198742.png

A crowd of people are seen by Penn Station during the COVID-19 pandemic in New York City on March 25, 2021. The mask mandate remains at the transit hub.Tayfun Coskun/Anadolu Agency via Getty ImagesCommuters board a Long Island Rail Road train at Penn Station in NYC on May 10, 2021.Amir Hamja/Bloomberg via Getty Images
1623479283721.png
Commuters board a Long Island Rail Road train at Penn Station in NYC on May 10, 2021.Amir Hamja/Bloomberg via Getty Images

Sometime in the next few days, New York will hit the milestone of 70 percent of eligible arms having at least one dose of vaccine. This will lift still further rules on commerce and congregation, but notably excepted are our schools, and yes, the poor souls waiting for their New Jersey or Long Island train lines. Why? Nobody seems to know, least of all Cuomo and his dour band of scientists.

Even worse is that the governor keeps talking about opening up to a “reimagined New York.” Reimagined by whom, to what purpose, and for whose benefit? Clearly Cuomo clings to his emergency powers so that he may be the one doing this reimagining, not the people of the state through their elected legislators. You know, how things are supposed to work.
David Marcus’ book, “Charade,” is now available.

Clear-minded New Yorkers know that two things have to happen in very short order. First, Cuomo’s emergency powers must be stripped. Second, the capricious and arbitrary rules on adults and even more importantly kids must be lifted. With positivity rates at an all-time low and vaccination rates sky-high, our schools and summer camps should return to normal, not a reimagined normal, but the normal of carefree capture the flag and archery we have always known.

All throughout the state, the confusing mandates have left people in churches, grocery stores and other public places doing a strange mask dance. If you’re vaccinated, why do you need to wear them? But as we know, there are still those who for myriad reasons having nothing to do with science cling to these security blankets.

The governor can and should end all of this by opening the state completely. Cuomo had no problem declaring his own victories in his ridiculous book last year, but now he won’t declare an actual victory over COVID bought with the effort of all New Yorkers.
 

Telescope Steve

Veteran Member
The mRNA "vaccines" could permanently change the DNA of the person injected. And that means that any children they have after the shot would have this newly changed DNA also.

New discovery shows human cells can write RNA sequences into DNA. That could be bad, if you are introducing RNA into cells which codes for something bad. The entire premise of the mRNA vaccine was predicted on the fact mRNA was a temporary signal that gets degraded shortly after injection, and then the signal is gone, as if it was never injected.


I found this story here:

 

TammyinWI

Talk is cheap
The mRNA "vaccines" could permanently change the DNA of the person injected. And that means that any children they have after the shot would have this newly changed DNA also.

New discovery shows human cells can write RNA sequences into DNA. That could be bad, if you are introducing RNA into cells which codes for something bad. The entire premise of the mRNA vaccine was predicted on the fact mRNA was a temporary signal that gets degraded shortly after injection, and then the signal is gone, as if it was never injected.


I found this story here:


Hello, with what I have come across, pertaining to how these "vaccines" are designed, no woman will be able to have a viable pregnancy after the shot/s. It is very disturbing, all of this is actually. If conception happens, the baby will die pre-birth, in many/most cases.

The info. on how this works and why, based on Gates and his cronies designed this, is described somewhere in articles on this forum, by those in the know/med pros.

So much info., don't even try to keep up with everything!
 

Telescope Steve

Veteran Member
Hello, with what I have come across, pertaining to how these "vaccines" are designed, no woman will be able to have a viable pregnancy after the shot/s. It is very disturbing, all of this is actually. If conception happens, the baby will die pre-birth, in many/most cases.

The info. on how this works and why, based on Gates and his cronies designed this, is described somewhere in articles on this forum, by those in the know/med pros.

So much info., don't even try to keep up with everything!
Thank you, I have read that also. These people are so sick with their plans to depopulate the world. Many people are having a hard time accepting this. It is a great awakening.
 

marsh

On TB every waking moment

NC Democrat Roy Cooper Refuses To Give Up Emergency Powers, Even When There Is No Emergency

By Kari Donovan
Published June 12, 2021 at 7:00am

Democrat Governor Roy Cooper refuses to give up the Emergency Powers he grabbed at the beginning of the COVID 19 Pandemic, and Republicans in the North Carolina General Assembly are tired of it according to the Senate President Pro Tempore.

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Senator Phil Berger (R-Caswell, Rockingham, Stokes, and Surry ) posted on Facebook:
“Gov. Cooper just EXTENDED his emergency order yet again. There is no emergency. This has got to end. We’re working on legislative action to curtail future abuses of the Governor’s executive authority.”
Local News WRAL reported on the matter:
“As other states end their state-of-emergency orders amid the waning coronavirus pandemic, Gov. Roy Cooper said Friday he wants to keep North Carolina’s in place.
“We are seeing tremendous improvement with fewer cases, hospitalizations, deaths and safety restrictions, but this is no time to hang up a ‘Mission Accomplished’ banner in our fight against the pandemic,” Cooper said in a statement. “We are laser focused on getting more shots in arms, boosting our economy and protecting unvaccinated people from the virus.”

The executive order he issued Friday runs through July 30 but doesn’t include any new restrictions. It does extend the state moratorium on evictions and flexibility with unemployment insurance.
Republican lawmakers sent a letter to Cooper this week pressing for the end of the state of emergency, noting that South Carolina Gov. Henry McMaster rescinded his state of emergency order on Monday and Virginia Gov. Ralph Northam plans to let his state’s expire at the end of this month.”
How did this guy win re-election when President Trump won the Presidential race in North Carolina? You would think someone in North Carolina would look into that.
 

marsh

On TB every waking moment

SHOCKING JUMP in Vaccine Deaths Reported This Week at CDC-Linked VAERS Tracking Website

By Jim Hoft
Published June 12, 2021 at 9:17am
There are more US deaths related to vaccines in 2021 in less than 5 months than there were the entire past decade.

The number of deaths linked to vaccines this year has absolutely skyrocketed. According to the CDC’s own data, in 2021 n the first 3 months, the VAERS website recorded over 1,750 deaths due to vaccines in the US.

That number is now at 5,997.

The Vaccine Adverse Event Reporting System (VAERS) database contains information on unverified reports of adverse events (illnesses, health problems and/or symptoms) following immunization with US-licensed vaccines. Reports are accepted from anyone and can be submitted electronically at www.vaers.hhs.gov.”
vaers-deaths.jpg


There were huge increases over last week. Deaths went up by an additional 700 in a week.

VAERS COVID Vaccine Data (Vaccine Adverse Events Reporting System, USA)

329,021 Reports Through June 4, 2021
DEATHS 5,888
HOSPITALIZATIONS 19,597
Urgent Care 43,891
OFFICE VISITS 58,800
ANAPHYLAXIS 1,459
BELL’S PALSY 1,737
Life Threatening 5,885
Heart Attacks 2,190
Myocarditis/Pericarditis 1,087
Thrombocytopenia/Low Platelet 1,564
Miscarriages 652
Severe Allergic Reaction 15,052
Disabled 4,583
 

Heliobas Disciple

TB Fanatic
This is a long article from back in Dec but I'm posting it in full, it takes a few posts. The link is questionable - I got a warning when I tried to open it that the page wasn't safe so I got the document off of google cache. Another reason to post the long article in full (to spare anyone having to navigate to another way of viewing it). - HD


Developers of Oxford-AstraZeneca Vaccine Tied to UK Eugenics Movement
(fair use applies)

Developers of Oxford-AstraZeneca Vaccine Tied to UK Eugenics Movement
The developers of the Oxford-AstraZeneca vaccine have previously undisclosed ties to the re-named British Eugenics Society as well as other Eugenics-linked institutions like the Wellcome Trust.
by Jeremy Loffredo and Whitney Webb
December 26, 2020

On April 30, AstraZeneca and the University of Oxford announced a “landmark agreement” for the development of a COVID-19 vaccine. The agreement involves AstraZeneca overseeing aspects of the development as well as manufacturing and distribution while the Oxford side, via the Jenner Institute and Oxford Vaccine Group, researched and developed the vaccine. Less than a month after this agreement was reached, the Oxford-AstraZeneca partnership was awarded a contract from the US government as part of Operation Warp Speed, the public-private COVID-19 vaccination effort dominated by the US military and US intelligence.

Though the partnership was announced in April, Oxford’s Jenner Institute had already begun developing the COVID-19 vaccine months before, in mid-January. According to a recent BBC report, it was in January that the Jenner Institute first became aware of how serious the pandemic would soon become, when Andrew Pollard, who works for the Jenner Institute and heads the Oxford Vaccine Group, “shared a taxi with a modeler who worked for the UK’s Scientific Advisory Group for Emergencies.” During the taxi ride, “the scientist told him data suggested there was going to be a pandemic not unlike the 1918 flu.” Because of this sole encounter, we are told, the Jenner Institute began to pour millions into the early development of a vaccine for COVID-19, well before the scope of the crisis was clear.

For much of 2020, the Oxford-AstraZeneca vaccine was treated as an early frontrunner, though its lead would later be marred by scandals related to its clinical trials, including the death of participants, sudden trial pauses, the use of a problematic “placebo” with its own host of side effects, and the “unintentional” misdosing of some participants that skewed its self-reported efficacy rate.

The significant issues that emerged during trials have provoked little concern from the vaccine’s two lead developers, despite critical attention from even mainstream media directed at its complications. The lead developer of the Oxford-AstraZeneca vaccine, Adrian Hill, told NBC on December 9 that the experimental vaccine should be approved and distributed to the public before the conclusion of the safety trials, saying “to wait for the end of the trial would be the middle of next year. That’s too late, this vaccine is effective, available at large scale and easily deployed.”

Sarah Gilbert, the other lead researcher on the vaccine, seemed to believe that premature safety approval was likely, telling the BBC on December 13 that the chances of rolling out the vaccine by the end of the year are “pretty high.” Now, the UK is expected to approve the Oxford-AstraZeneca vaccine shortly after Christmas, with India also set to approve the vaccine next week.

While the controversies surrounding the vaccine’s trials did ultimately undermine its previous frontrunner status, the Oxford-AstraZeneca vaccine remains heavily promoted as the vaccine of choice for the developing world, as it is cheaper and has much less complicated storage requirements than its main competitors, Pfizer and Moderna.

Earlier this month, Richard Horton, editor in chief of the Lancet medical journal, told CNBC that “the Oxford-AstraZeneca vaccine is the vaccine right now that is going to be able to immunize the planet more effectively, more rapidly than any other vaccine we have,” in large part because it is a “vaccine that can get to lower-middle-income countries.” CNBC also quoted Andrew Baum, global head of health care for Citi Group, as saying that the Oxford-AstraZeneca vaccine “is really the only vaccine that is going to suppress or even eradicate SARS-CoV-2, the virus that causes COVID-19, in the many millions of individuals in the developing world.”

In addition to longstanding claims that the Oxford-AstraZeneca vaccine will be the vaccine of choice for the developing world, this vaccine candidate has also been treated by several outlets in the mainstream, and even independent media, as “good for people, bad for profits” due to the partnership’s “explicit intention of supplying [the vaccine] around the world on a not-for-profit basis, meaning that the poorest nations on the planet will not have to worry about being shut out of a cure due to lack of funds.”

However, investigation into the vaccine’s developers and the realities of their “no-profit pledge” reveals a very different story than that which has been spun for most of the year by corporate press releases, experts, and academics tied to the vaccine and the mainstream press.

For instance, mainstream media has had little, if anything, to say about the role of the vaccine developers’ private company—Vaccitech—in the Oxford-AstraZeneca partnership, a company whose main investors include former top Deutsche Bank executives, Silicon Valley behemoth Google, and the UK government. All of them stand to profit from the vaccine alongside the vaccine’s two developers, Adrian Hill and Sarah Gilbert, who retain an estimated 10 percent stake in the company. Another overlooked point is the plan to dramatically alter the current sales model for the vaccine following the initial wave of its administration, which would see profits soar, especially if the now-obvious push to make COVID-19 vaccination an annual affair for the foreseeable future is made reality.

Arguably most troubling of all is the direct link of the vaccine’s lead developers to the Wellcome Trust and, in the case of Adrian Hill, the Galton Institute, two groups with longstanding ties to the UK eugenics movement. The latter organization, named for the “father of eugenics” Francis Galton, is the renamed UK Eugenics Society, a group notorious for over a century for its promotion of racist pseudoscience and efforts to “improve racial stock” by reducing the population of those deemed inferior.

The ties of Adrian Hill to the Galton Institute should raise obvious concerns given the push to make the Oxford-AstraZeneca vaccine he developed with Gilbert the vaccine of choice for the developing world, particularly countries in Latin America, South and Southeast Asia, and Africa, the very areas where the Galton Institute’s past members have called for reducing population growth.

In the final installment of this series on Operation Warp Speed, the US government’s vaccination effort and race, the Oxford-AstraZeneca vaccine’s ties to eugenics-linked institutions, the secretive role of Vaccitech, and the myth of the vaccine’s sale being “nonprofit” and altruistically motivated are explored in detail.

GlaxoSmithKline and the Jenner Institute

The Edward Jenner Institute for Vaccine Research was initially established in 1995 in Compton in Berkshire as a public-private partnership between the UK government, via the Medical Research Council and the Department of Health, and the pharmaceutical giant GlaxoSmithKline. Following a “review by the [institute’s] sponsors,” it was relaunched in 2005 in Oxford under the leadership of Adrian Hill, who—prior to that appointment—held a senior position at the Wellcome Trust’s Centre for Human Genetics. Hill, the lead developer of the Oxford-AstraZeneca COVID-19 vaccine, still leads a research group at Wellcome aimed at “understand[ing] the genetic basis of susceptibility to different infectious diseases, especially. . . severe respiratory infections,” which conducts most of its studies in Africa. The UK’s Medical Research Council has also become a collaborator with the Wellcome Trust, specifically on vaccine-related initiatives. The Wellcome Trust, discussed at greater length later in this article, was originally created with funding from Henry Wellcome, who founded the company that later became GlaxoSmithKline.

Hill’s partner at the Jenner Institute and the other co-developer of the Oxford COVID-19 vaccine is Sarah Gilbert. Gilbert also hails from the Wellcome Trust, where she was a “program director,” and is a student of Hill’s. Together, Gilbert and Hill have worked to position the institute to be the center of all future vaccination efforts undertaken in response to global pandemics.

The Jenner Institute’s relocation to Oxford was largely facilitated by the Medical Research Council, which donated £1.25 million between 2005 and 2006, after the decision was made to replace the institute’s original sponsors (GlaxoSmithKline, the Medical Research Council, the Department of Health) with the University of Oxford and the Institute for Animal Health, now called the Pirbright Institute. The involvement of Pirbright meant that the relaunched Jenner Institute became unique in developing vaccines for both humans and livestock.

The relaunched Jenner Institute has come to dominate publicly funded vaccine development in the UK as well as the testing of vaccines produced by the world’s largest pharmaceutical companies via clinical trials and has overseen prominent safety trials for vaccines of high media interest in recent years. Some of the Jenner Institute–conducted trials later draw controversy, such as those using South African infants in 2009 in which seven infants died.

An investigation conducted by the British Medical Journal found that the Hill-led Jenner Institute had, in the South African instance, knowingly misled parents about the negative results of and questionable methods used in animal studies as well the vaccine being known to be ineffective. The vaccine in question, an experimental tuberculosis vaccine developed jointly by Emergent Biosolutions and the Jenner Institute, was scrapped after the controversial study in infants confirmed what was already known, that the vaccine was ineffective. The trial, largely funded by Oxford and the Wellcome Trust, was subsequently praised as “historic” by the BBC. Hill, at the time the study was conducted, had a personal financial stake in the vaccine.

Similar instances of dodgy practices in efficacy trials and the effects of increased dosages have led vaccine experts to criticize the COVID-19 vaccine developed by Hill and Gilbert. Hill and Gilbert hold a considerable financial stake in the Oxford-AstraZeneca COVID-19 vaccine. While the vaccine reportedly has an efficacy of over 90 percent, those figures—often cited in mainstream reports—are self-reported by the vaccine’s developers and manufacturers (i.e., the Oxford team and AstraZeneca), which is significant given that Hill and other Jenner Institute scientists have previously been caught manipulating trial results to benefit a vaccine product in which they were personally invested.

The prominence of the Jenner Institute in vaccine development and testing has largely come through Hill’s additional leadership role at the UK’s Vaccines Network, which chooses what vaccines to develop, how to develop them, and which firms should receive “targeted investments” from the UK government. The Vaccines Network also plays a key role in identifying “what vaccine technologies could play an important role in future outbreaks.” Two of the main backers of the UK’s Vaccines Network are the Wellcome Trust and GlaxoSmithKline.

Unsurprisingly, the Vaccines Network has steered many millions of pounds toward the Hill-run Jenner Institute, with completed projects including a “plug and display” virus-like particle platform for rapid-response vaccination. Also funded by the Vaccines Network were the Jenner Institute’s initial studies of novel chimpanzee adenovirus vaccines for coronavirus (in this case, MERS), the same viral vector used for the Oxford-AstraZeneca vaccine. In addition to the Vaccines Network, the Jenner Institute also coordinates the efforts of the EU’s Vaccines Network equivalent, MultiMalVax.

The Jenner Institute also has a close relationship with GlaxoSmithKline and the Italian biotech Okairos, which was acquired by GlaxoSmithKline in 2014. Soon after it was acquired, Okairos, and its new owner GlaxoSmithKline, became key players in the 2014 experimental Ebola vaccine push, an effort that mirrors the current COVID-19 vaccine development rush in many key ways. The rushed safety trials for that vaccine were overseen by Adrian Hill and the Jenner Institute and funded by the UK government and the Wellcome Trust. GlaxoSmithKline and Okairos are the only firms represented on the Jenner Institute’s Scientific Advisory Board.

The Jenner Institute along with GlaxoSmithKline-Okairos and a small French biotech called Imaxio have been developing an experimental malaria vaccine since 2015, with human trials of that vaccine announced on December 12, 2020. Those trials will be conducted on 4,800 children in Africa over the course of 2021, in many of the same countries where Hill’s research group at the Wellcome Center for Human Genetics has been studying genetic susceptibility to several diseases. “A lot more people will die in Africa this year from malaria than will die from Covid,” Hill recently said in regard to the soon-to-begin trials.

Currently, the Jenner Institute is funded by the Jenner Vaccine Foundation, but the foundation’s documents note on several occasions a considerable influx of money from Wellcome Trust Strategic Awards. A “special review panel” from the Wellcome Trust actually lobbied the Jenner Institute to apply for further “strategic core funding” from the trust after visiting the institute and appraising its work. The Jenner Institute frames its funding from Wellcome as the key guidance behind its development decisions, which are made “based on the successful model of Wellcome Trust Strategic Award support.”

The Jenner Institute’s foundation, however, is not the only source of income for its lead researchers. Hill and Gilbert have been working to commercialize many of the institute’s vaccines through their own private company, Vaccitech. Though media reports often describe the vaccine as being a joint effort between AstraZeneca and the University of Oxford, Vaccitech is a key stakeholder in that partnership, given that the vaccine candidate relies on technology developed by Hill and Gilbert and owned by Vaccitech. A deeper look into Vaccitech offers a clue as to why the company’s name has been absent from nearly all media reports on the Oxford-AstraZeneca vaccine, as it demolishes the much-touted claim that the vaccine is “nonprofit” and offered at low cost for charitable reasons.

[continued next post]
 
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Heliobas Disciple

TB Fanatic
Vaccitech: Doing Well by Doing “Good”?

The official reason Sarah Gilbert and Adrian Hill created Vaccitech in 2016 perThe Times is because “Oxford’s researchers [are] encouraged to form companies to commercialize their work.” Vaccitech, like other “commercialized” Oxford research enterprises, was spun out of the Jenner Institute via the university’s commercialization arm, Oxford Science Innovations, which is currently Vaccitech’s largest stakeholder at 46 percent. Hill and Gilbert are reported to maintain a 10 percent stake in the company.

The largest investor in Oxford Science Innovations, and by extension one of the largest shareholders in Vaccitech, is Braavos Capital, the venture-capital firm started in 2019 by Andrew Crawford-Brunt, Deutsche Bank’s long-time global head of equity trading at its London branch. Through its stake in Oxford Science Innovations, Braavos owns about 9 percent of Vaccitech.

Prior to COVID-19, Vaccitech’s main focus, especially last year, was the development of a universal vaccine for the flu. Vaccitech’s efforts in this regard were praised by Google, which is also invested in Vaccitech. At the same time, the Bill & Melinda Gates Foundation was funding research to develop a universal flu vaccine, reportedly because the field of influenza vaccinology was not yet able “to design a flu vaccine that would protect broadly against the strains of flu that infect people every winter and those in nature that could emerge to trigger a disruptive and deadly pandemic,” according to a STAT News report from last year. The Gates Foundation effort originally partnered with Google’s cofounder Larry Page and his wife Lucy.

To fully finance Hill and Gilbert’s Vaccitech, and specifically its quest to develop a universal flu vaccine, Oxford Science Innovations sought £600 million from “outside investors,” chief among them the Wellcome Trust and the venture-capital arm of Google, Google Ventures. This means that Google is poised to make a profit from the Oxford-AstraZeneca vaccine at a time when its video platform YouTube has moved to ban COVID-19 vaccine–related content that shines a negative light on COVID-19 vaccines, including the Oxford-AstraZeneca candidate. Other investors in Vaccitech include Sequoia Capital’s Chinese branch and the Chinese pharmaceutical company Fosun Pharma. In addition, the UK government has put an estimated £5 million into the company and is also expected to make a return on the Oxford-AstraZeneca vaccine.

Information on the profit motive behind the Oxford-AstraZeneca vaccine has been muddied due to the extensive media promotion of the claim that Hill and Gilbert will not be collecting royalties on the vaccine and that AstraZeneca is not making a profit off the vaccine. However, this is only true until the pandemic is “officially” declared over, and the virus is labeled a persistent or seasonal condition that will require the mass administration of COVID-19 vaccines at regular intervals and possibly annually. Sky News reported that the determination of when the pandemic is over “will be based on the views of a range of [unspecified] independent bodies.” At that point, both Vaccitech and Oxford will obtain royalties from AstraZeneca’s sales of the vaccine.

Those tied to the vaccine have been at the center of promoting the idea that the COVID-19 vaccine will soon become an annual affair. For instance, in early May, John Bell—an Oxford medical professor and an “architect” of the Oxford-AstraZeneca partnership—told NBC News, “I suspect we may need to have relatively regular vaccinations against coronaviruses going into the future,” adding that the vaccine would likely be needed every year like the flu vaccine. NBC News failed to note that the Oxford-AstraZeneca vaccine in which Bell is involved stands to significantly benefit financially if that does come to pass.

More recently, Bell told The Week that, “should there prove to be a market for regular vaccinations against coronavirus in the future, ‘there is some money to be made.’” Such sentiments have been echoed by Pascal Soriot, the CEO of AstraZeneca, who told Bloomberg last month that the company stood to make a “reasonable profit” once the pandemic was declared over and COVID-19 deemed a seasonal illness requiring regular vaccinations. On this matter, Vaccitech’s CEO, Bill Enright, stated that Vaccitech investors would receive a “big chunk of the royalties from a successful vaccine as well as ‘milestone’ payments” if and when the pandemic is declared over and COVID-19 vaccines become a seasonal event.

Vaccitech, in particular, appears quite certain that this possibility is slated to become reality. For all subsequent iterations of the Oxford-AstraZeneca vaccine, Vaccitech will reacquire a much larger percentage of rights to the vaccine, rights it is currently splitting with Oxford for the first iteration. Sky News has noted that the technology that Vaccitech owns “could drive the second generation of COVID-19 vaccines” and that it “has [already] received £2.3 million of public funding to develop it.”

US government officials such as Anthony Fauci have also signaled that the COVID-19 vaccine will require annual shots. Notably, the government, through Health and Human Service’s BARDA, has poured over $1 billion into the Oxford-AstraZeneca vaccine development. In addition to government officials, several recently published mainstream media reports have claimed that the “expert” consensus “seem to be leaning toward an annual shot like the flu vaccine” with regard to the COVID-19 vaccine. For instance, Charles Chiu, a professor of infectious diseases at the University of California–San Francisco, recently told Salon, “This may end up being a vaccine that’s not a one-time thing or even a two-time thing . . . it may end up being what we call either a seasonal vaccine, or vaccine that needs to be administered every couple of years.”

Such hints about an annual COVID-19 vaccine from 2021 onward have recently become commonplace from the leading COVID-19 vaccine manufacturers themselves. For instance, on December 13, Pfizer CEO Albert Bourla was quoted by the Telegraph as saying, “How long this [vaccine] protection lasts is something we don’t know . . . I think it is a likely scenario that you will need periodical vaccinations.” Pfizer also recently issued a statement that noted that “we don’t know how the virus will change, and we also don’t know how durable the protective effect of any vaccination will be,” adding that its vaccine would be suitable “for repeated administration as booster shots” in the event that the vaccine only induces an immune response for a few months.

Then, this past Tuesday, Moderna released information that suggested immunity from its COVID-19 vaccine would only last several months, with Forbes writing that “the duration of neutralizing antibodies from the Moderna vaccine will be relatively short, potentially less than a year,” an outcome that would favor the push for an annual COVID-19 shot. The developer of the Pfizer COVID-19 vaccine, Ugur Sahin of BioNTech, also stated on Tuesday that “the virus will stay with us for the next 10 years. . . . We need to get used to the fact there’ll be more outbreaks.” He later added that “if the virus becomes more efficient . . . we might need a higher uptake of the vaccine for life to return to normal,” implying that these regular outbreaks he foresees occurring over the next ten years would be correlated with increased vaccine administration.

Quotes from the developers of the Oxford-AstraZeneca vaccine themselves also point to a pandemic-dominated future and a desire for the crisis to be prolonged so that the vaccine can be widely distributed. Gilbert told the UK Independent in August that she believes COVID-19 is just the beginning and that COVID-like pandemics will become more frequent in the near future. The Jenner Institute vaccine team seems so determined to create the COVID vaccine that, in June, Hill was quoted by the Washington Post as stating that he wanted the pandemic to stick around, saying, “We’re in the bizarre position of wanting COVID to stay, at least for a little while. But cases are declining.” He also stated that his team was in “a race against the virus disappearing.”

With the vaccine developers, “medical experts,” government officials, and the CEOs of major vaccine manufacturers all agreeing that a seasonal COVID-19 vaccine is an increasingly likely outcome, it is worth considering a possible ulterior motive regarding the initial “nonprofit” model being used by the Jenner Institute/Vaccitech and AstraZeneca for their joint COVID-19 vaccine.

Given that vaccine guidance in several countries states that each dose of the multidose COVID-19 vaccine must be produced by the same manufacturer as previous doses, the implication is that in the event of a need for periodic COVID-19 vaccine variants, those who initially received the Oxford-AstraZeneca vaccine would likely be required to receive that same “brand” of vaccine seasonally. In other words, those who initially received the Oxford-AstraZeneca vaccine would likely be required, not just to receive a second dose of the same “brand,” but continue receiving that same “brand” of vaccine every year. Notably, no interaction studies have yet been conducted on the interactions between the COVID-19 vaccines and other medications as well as other vaccines.

If this turns out to be the case, it would certainly behoove the Oxford-Vaccitech-AstraZeneca team to want their vaccine to be the most widely used one in the first year in order to guarantee the largest market for subsequent annual COVID-19 vaccines. This could be a possible motive behind the efforts of the Oxford-AstraZeneca partnership “to supply the entire world with the Oxford jab” and to supply the vaccine “to the most vulnerable groups to COVID-19.” This vaccine has already been purchased, even before regulatory approval, by governments around the world, including in Europe, North America, Australia, and most Latin American countries.

The Wellcome Trust

Adrian Hill currently holds a senior position at the Wellcome Trust’s Centre for Human Genomics. The Wellcome Trust is a scientific charity based in London, established in 1936 with funds from pharmaceutical magnate Henry Wellcome. As previously mentioned, Wellcome founded the pharmaceutical company that eventually became the industry giant GlaxoSmithKline. Today, the Wellcome Trust has a $25.9 billion endowment and engages in philanthropic endeavors, including funding clinical trials and research.

Hill has been closely tied to Wellcome for decades. In 1994, he participated in the founding of the Wellcome Centre for Human Genetics and was awarded a Wellcome Trust Principal Research Fellowship the following year. He became a Wellcome professor of human genetics in 1996.

The Wellcome Centre for Human Genetics website boasts of the large-scale genetic mapping they’ve conducted in Africa. The center also publishes papers that explore genetic dispositions in relation to male fertility and “reproductive success.” The crossroads between race and genes is important in the center’s work, as an entire working group at the center, the Myers Group, is dedicated to mapping the “genetic impacts of migration events.” The center also funded a paper that argued that so long as eugenics is not coercive it’s an acceptable policy initiative. The paper asks, “Is the fact that an action or policy is a case of eugenics necessarily a reason not to do it?” According to Hill’s page on the Wellcome Trust site, race and genetics have long played a central role in his scientific approach, and his group currently focuses on the role genetics plays in African populations with regard to susceptibility to specific infectious diseases.

[cont next post]
 

Heliobas Disciple

TB Fanatic
Of even greater concern, last year Science Mag reported that Wellcome was accused by both a whistleblower and the University of Cape Town South Africa of illegally exploiting hundreds of Africans by “commercializing a gene chip without proper legal agreements and without the consent of the hundreds of African people whose donated DNA was used to develop the chip.” Jantina de Vries, a bioethicist at the University of Cape Town South Africa, told the journal that it was “clearly unethical.” Since the controversy, other African institutions and peoples such as the indigenous Nama people of Namibia have demanded that Wellcome return the DNA it collected.

The Wellcome Centre regularly cofunds the research and development of vaccines and birth control methods with the Gates Foundation, a foundation that actively and admittedly engages in population and reproductive control in Africa and South Asia by, among other things, prioritizing the widespread distribution of injectable long-acting reversible contraceptives (LARCs). The Wellcome Trust has also directly funded studies that sought to develop methods to “improve uptake” of LARCs in places such as rural Rwanda.

As researcher Jacob Levich wrote in the Palgrave Encyclopedia of Imperialism and Anti-Imperialism, LARCs afford women in the Global South “the least choice possible short of actual sterilization.” Some LARCs can render women infertile for as long as five years, and, as Levich argues, they “leave far more control in the hands of providers, and less in the hands of women, than condoms, oral contraceptives, or traditional methods.”

One example is Norplant, a contraceptive implant manufactured by Schering (now Bayer) that can prevent pregnancy for up to five years. It was taken off the US market in 2002 after more than fifty thousand women filed lawsuits against the company and the doctors who prescribed it. Seventy of those class action suits were related to side effects such as depression, extreme nausea, scalp-hair loss, ovarian cysts, migraines, and excessive bleeding.

The Galton Institute: Eugenics for the Twenty-First Century

Both the Wellcome Trust and Adrian Hill share a close relationship with the most infamous eugenics society in Europe, the British Eugenics Society. The Eugenics Society was renamed the Galton Institute in 1989, a name that pays homage to Sir Francis Galton, the so-called father of eugenics, a field that he often described as the “science of improving racial stock.”

In the case of the Wellcome Trust, the Trust’s library is the guardian of the Eugenics Society historical archives. When the Wellcome Trust first set up its Contemporary Medical Archive Center, the first organizational archive it sought to acquire was tellingly that of the Eugenics Society–Galton Institute. Wellcome’s website describes the Eugenics Society’s original purpose as “to increase public understanding of heredity and to influence parenthood in Britain, with the aim of biological improvement of the nation and mitigation of the burdens deemed to be imposed on society by the genetically ‘unfit’.” It also states the interests of the society’s members “ranged from the biology of heredity, a subject that developed rapidly during the first half of the 20th century, to the provision of birth control methods, artificial insemination, statistics, sex education and family allowances.” Lesley Hall, Wellcome’s senior archivist, has referred to Francis Galton, a racist eugenicist, as an “eminent late nineteenth century polymath” in her discussion of the Eugenics Society archive held at Wellcome.

Eugenics_Society_Poster_1930s-1024x665.png

A poster published by the Eugenics Society-Galton Institute in the 1930S, from the Wellcome Library

Several top governance positions at the former British Eugenics Society, now the Galton Institute, include individuals who originally worked at the Wellcome Trust, including the Galton Institute’s president Turi King. Elena Bochukova, a current Galton Council Member and Galton lecturer, previously worked under the direction of Adrian Hill at the Wellcome Trust Centre for Human Genetics. The Galton Institute’s senior genetics researcher, Jess Buxton, was previously a “genetics researcher” at the Wellcome Trust and then went on to carry out independent research financed by Wellcome. Her research, which is particularly race oriented, includes creating the first genetic sequence map of a native Nigerian. Moreover, Adrian Hill himself spoke at the Eugenics Society–Galton Institute at the celebration of their 100th anniversary in 2008.

The Galton Institute publishes what they now call the Galton Review, previously titled the Eugenics Review, where various members of the self-proclaimed “learned society” publish papers focused on population issues, genetics, evolutionary biology, and fertility.

A look at early issues of the Eugenics Review shines a light on Galton’s original ambitions. In the 1955 issue titled “The Immigration of Colored People,” an author asks, “What will become of our national character, good workmanship etc. in the course of a few decades if this immigration of negroes and negroids continues unchecked?” The article ends with an appeal to readers to write their parliamentary representatives and urge them that in view of “racial betterment or deterioration” something must be done urgently to “check the present influx of africans and other negroids.”

Today, it appears that the Galton Institute continues to see the immigration of racial minorities into European cities as an unchecked threat. David Coleman, an Oxford professor of demographics and a fellow at the institute runs an anti-immigration organization and advocacy group called MigrationWatch, whose mission is to preserve the European culture of the UK by lobbying the government to stem legal immigration and publishing data that supposedly demonstrates the biological and cultural threat of increasing immigration.

A 1961 issue of the Eugenics Review titled “The Impending Crisis” claims the function of the institute’s upcoming conference is “to honor Margaret Sanger” and describes the population crisis as “quantity threatening quality.”

Sanger, known as the “pioneer of the American birth control movement,” was a staunch advocate for promoting “racial betterment” and the key architect of the Negro Project, which she claimed “was established for the benefit of the colored people.” But as medical ethics fellow at Harvard Medical School, Harriet Washington, argues in her book Medical Apartheid, “The Negro Project sought to find the best way to reduce the black population by promoting eugenic principals.” Sanger was an American member of the British Eugenics Society.

Another early member of the Galton Institute was John Harvey Kellogg, prominent business man and eugenicist. Kellogg founded the Race Betterment Foundation and argued that immigrants and nonwhites would damage the American gene pool. Yet another example is Charles Davenport, a scientist known for his collaborative research efforts with eugenicists in Nazi Germany and his contributions to Nazi Germany’s brutal racial policies, who was vice president of the Galton Institute in 1931.

Another more recent member of the Galton Institute was David Weatherall, for whom the Weatherall Institute of Molecular Medicine at Oxford is named. Weatherall was a member of the Galton Institute when it was still named the Eugenics Society, and he remained a member until his death in 2018. Weatherall, who was knighted by the British monarch in 1987 for his contributions to science, addressed the Galton Institute on numerous occasions and gave a senior lecture on genetics at the institute in 2014, of which no transcript or video is available. As an Oxford professor, Weatherall was Adrian Hill’s doctoral adviser and eventually his boss when Hill began working at the Weatherall Institute conducting immunogenic research in Africa. A key fixture of the Weatherall Institute of Molecular Medicine since its founding is Walter Bodmer, a former president of the Galton Institute.

While the Galton Institute has attempted to distance itself from its past of promoting racial eugenics with surface-level public relations efforts, it has not stopped family members of the infamous racist from achieving leadership positions at the institute. Emeritus professor of molecular genetics at the Galton Institute and one of its officers is none other than David J. Galton, whose work includes Eugenics: The Future of Human Life in the 21st Century. David Galton has written that the Human Genome Mapping Project, originally dreamt up by Galton’s former president Walter Bodmer, had “enormously increased . . . the scope for eugenics . . . because of the development of a very powerful technology for the manipulation of DNA.”

This new “wider definition of eugenics,” Galton has said, “would cover methods of regulating population numbers as well as improving genome quality by selective artificial insemination by donor, gene therapy or gene manipulation of germ-line cells.” In expanding on this new definition, Galton is neutral as to “whether some methods should be made compulsory by the state, or left entirely to the personal choice of the individual.”

Slightly modified and rebranded as Jadelle, the dangerous drug was promoted in Africa by the Gates Foundation in conjunction with USAID and EngenderHealth. Formerly named the Sterilization League for Human Betterment, EngenderHealth’s original mission, inspired by racial eugenics, was to “improve the biological stock of the human race.” Jadelle is not approved by the FDA for use in the United States.

Another scandal-ridden LARC is Pfizer’s Depo-Provera, an injectable contraceptive used in several African and Asian countries. The Gates Foundation and USAID have collaborated to fund this drug’s distribution and introduce it into the health-care systems of countries including Uganda, Burkina Faso, Nigeria, Niger, Senegal, Bangladesh, and India.

Andrew Pollard, director of the Oxford Vaccine Group, where Hill’s Jenner Institute resides, is enmeshed with the Gates Foundation. His employer, the University of Oxford, has received $11 million for vaccine development research from the foundation over the past three years and $208 million in grants over the past decade. In 2016, the Gates Foundation gave $36 million to a team of researchers that was headed by Pollard for vaccine development. In addition, Pollard’s private laboratory is funded by the Gates Foundation. Given this, it should come as no surprise that the Global Alliance for Vaccine Initiative (GAVI), a public-private partnership founded and currently funded by the Bill & Melinda Gates Foundation, plans to distribute the Oxford-AstraZeneca COVID-19 vaccine to low-income, predominantly African and Asian, countries once it’s approved.

[cont next post]
 

Heliobas Disciple

TB Fanatic
Who Gets the Safest Vaccines?

Considering the degree to which the players and institutions behind the Oxford-AstraZeneca vaccine (including the lead developer) are tied and connected to institutions that have been instrumental in the rise and perpetuation of racial eugenics, it’s concerning that this particular vaccine is being portrayed by scientists and media alike as the COVID-19 vaccine for the poor and the Global South.

The Oxford-AstraZeneca vaccine sells at a fraction of the cost of its COVID-19 vaccine competitors—running between 3 and 5 dollars per dose. Moderna and Pfizer cost 25 to 37 dollars and 20 dollars per dose, respectively. As CNN recently reported, the Oxford-AstraZeneca vaccine will “be far easier to transport and distribute in developing countries than its rivals,” several of which require complicated and costly cold supply chains. When the Thomson Reuters Foundation asked several experts which COVID-19 vaccine could “reach the poorest soonest,” all declared a preference for the Oxford-AstraZeneca candidate.

There is also the added fact that a host of safety issues have come to surround the vaccine. Recently, on November 21, a forty-year-old participant in AstraZeneca’s clinical trial who lives in India sent a legal notice to the Serum Institute of India alleging that the vaccine caused him to develop acute neuroencephalopathy, or brain damage. In the notice, the participant said he “must be compensated, in the least, for all the sufferings that he and his family have undergone and are likely to undergo in the future.”

In response, the Serum Institute claimed the participant’s medical complications are unrelated to the vaccine trial and said it would take “legal action” against the brain-damaged participant for maligning the company’s reputation, seeking damages in excess of $13 million. “This is the first time I have ever heard of a sponsor threatening a trial participant,” Amar Jesani, editor of the Indian Journal of Medical Ethics, said of the incident. The Serum Institute has received at least $18.6 million from the Bill & Melinda Gates Foundation and has a deal with AstraZeneca to manufacture a billion doses of the vaccine.

Other manufacturers chosen by Oxford-AstraZeneca to produce their vaccine are also no strangers to controversy. For instance, their manufacturing partner in China, Shenzhen Kangtai Biological Products, has been at the center of controversy for years, especially after seventeen infants died from its hepatitis B vaccine in 2013. The New York Times cited Yanzhong Huang, a senior fellow for global health at the Council on Foreign Relations, as saying, “Imagine if a similar scandal is reported again in China. . . . It’s not just going to undermine the confidence of the company manufacturing the vaccine, it’s also going to hurt the reputation of AstraZeneca itself and their vaccine, too.”

In another example, the manufacturing partner chosen to produce the vaccine in the US is the scandal-ridden company with ties to the 2001 anthrax attacks, Emergent Biosolutions. Emergent Biosolutions, previously known as BioPort, has a long track record of knowingly selling and marketing products that were never tested for safety and efficacy, including its anthrax vaccine BioThrax and its biodefense product Trobigard. The current head of quality control for Emergent Biosolutions’ lead manufacturing facility in the US has no expertise in pharmaceutical manufacturing and is instead a former high-ranking military intelligence official who operated in Iraq, Afghanistan, and beyond.

The issues raised by their decision to partner with manufacturers with dark histories of product safety issues are compounded by the adverse reactions reported in the Oxford-AstraZeneca trials as well as the ways in which those trials have been conducted. In September, AstraZeneca was forced to pause its experimental COVID-19 vaccine trial after a woman in the UK developed a “suspected serious reaction” that the New York Times reported was consistent with transverse myelitis. TM is a neurological disorder characterized by inflammation of the spinal cord, a major element of the central nervous system. It often results in weakness of the limbs, problems emptying the bladder, and paralysis. Patients can become severely disabled, and there is currently no effective cure.

Concern over an association between TM and vaccines is well established. A review of published case studies in 2009 documented thirty-seven cases of TM associated with various vaccines, including hepatitis B, measles-mumps-rubella, diphtheria, pertussis, tetanus, among others in infants, children, and adults. The researchers in Israel noted, “The associations of different vaccines with a single autoimmune phenomenon allude to the idea that a common denominator of these vaccines, such as an adjuvant, might trigger this syndrome.” Even the New York Times article on the AstraZeneca trial pause notes past “speculation” that vaccines might be able to trigger TM.

In July, an Oxford-AstraZeneca trial participant developed symptoms of TM, and the vaccine trial was paused at that time. An “independent panel” ultimately concluded the illness was unrelated to the vaccine, and the trial continued. Yet, as Nikolai Petrovsky from Flinders University told the Australian Broadcasting Corporation, these panels are typically made up of “biostatisticians and also medical representatives from the sponsor drug company running the trial.” Then, in October, a trial participant in Brazil died, though in that case, AstraZeneca suggested that the person was part of the control group and thus hadn’t received the COVID-19 vaccine.

According to Forbes, the AstraZeneca vaccine was ineffective at stopping the spread of coronavirus in their animal trials. All six monkeys injected with AstraZeneca’s COVID-19 vaccine became infected with the disease after being inoculated. All the monkeys were put to death, which means that it will remain unknown whether those monkeys would have suffered other adverse effects.

Another concern is that trial administrators gave the trial control group (for both human and animal trials) Pfizer’s Nimenrix, a meningitis vaccine, as opposed to a saline solution, which is regarded as the gold standard for controls because researchers can be sure the saline solution won’t cause any adverse reactions. Using Pfizer’s meningitis vaccine as the control placebo allows AstraZeneca to downplay any adverse reactions in its COVID-19 vaccine group by showing that the control group suffered adverse reactions as well. “The meningitis vaccine in the AstraZeneca trial is what I would call a ‘fauxcebo,’ a fake control whose real purpose is to disguise or hide injury in the vaccine group,” said Mary Holland, general counsel at Children’s Health Defense.

Eugenics under Another Name

Despite these safety concerns and clinical trial scandals, close to 160 countries have purchased the Oxford-AstraZeneca vaccine, and now reports are suggesting that India, the country with the second largest population on earth, is likely to approve this vaccine by next week.

As documented here, while the vaccine may be heralded as “vital for lower-income countries,” the Oxford-AstraZeneca project is no mere philanthropic pursuit. Not only is there a significant profit motive behind the vaccine, but its lead researcher’s connection to the British Eugenics Society adds another level of warranted scrutiny.

For those encountering stories of eugenicists, it’s common to dismiss such activity as that of “conspiracy theories.” However, it’s undeniable that several prominent individuals and institutions that remain active today have clear ties to eugenicist thinking, which was not so taboo just a few decades ago. Unfortunately, this holds true for the individuals and institutions associated with the Oxford-AstraZeneca COVID vaccine, who, as demonstrated in this article, immerse themselves in studies of race science and population control—primarily in Africa—while working closely with institutions that have direct and longstanding links to the worst of the eugenics movement.

As this series has shown, there are many concerns regarding the points where race and the COVID-19 vaccination campaign in the US and abroad intersect, both publicly and privately. Part 1 of this series raised questions about the policy-shaping role of the Johns Hopkins Center for Health Security, which suggested that the US government make COVID-19 vaccines available to ethnic minorities and the mentally challenged first. Part 2 explained how in order to allocate COVID-19 vaccines in the US, health agencies are using a program created by Palantir, a company with a record of helping the US agencies target ethnic minorities through immigration policy and racist policing.

Furthermore, there are plans in place to exercise what could reasonably be described as economic coercion to pressure people to “voluntarily” get vaccinated. Such coercion will be obviously be more effective on poor and working communities, meaning communities of color will be disproportionately affected as well.

Considering these facts, and the case for scrutinizing the safety of Oxford-AstraZeneca’s “affordable” vaccine option made above, any harm caused by vaccine allocation policy in the US and beyond is likely to disproportionately affect poor communities, especially communities of color.

As such, the public should take all vaccine rollout policy assertions with a grain of salt, even when they come cloaked in language of inclusion, racial justice, and public health preservation. As the cofounder of the American Eugenics Society (later renamed Society for the Study of Social Biology) Frederick Osborn put it in 1968, “Eugenic goals are most likely to be attained under a name other than eugenics.”

[end of article]
 

Heliobas Disciple

TB Fanatic
Interestingly, this video is all about why the Welcome Trust is so involved in a conference call with Fauci. (see article above for more on the trust)

Fauci's Dishonesty and Co-Conspirators Revealed!
Premiered Jun 4, 2021
39min 22sec

View: https://www.youtube.com/watch?v=DNxoVFZwMYw
Peak Prosperity
In this episode, I break down a very short window of time from Jan 31, 2020 to Feb 2 - 2020 when Fauci met with key representatives of the Wellcome Trust, WHO, NIH and senior private virologists. They presumably discussed prior and ongoing gain of function experiments on SARS CoV viruses as well as the lab leak origin theory that was worriedly gaining steam out in the public eye. Mere days after this meeting a wall of scientific opinion coupled to air-tight media backing concluded that SARS-CoV-2 could not have come from a lab but must have been of natural origin. We now know this was not based on science but was a predetermined conclusion in search of supporters and which made declarative statements that could not possibly have been grounded in actual science.
 

raven

TB Fanatic
look at the bright side
If you've "never been sick a day in your life" and there is not hereditary disease in your DNA
then you got a golden ticket.
but if you think it is going to decrease your health insurance premium
you are not paying attention.
 

marsh

On TB every waking moment

BOOM! Florida Court Rules Mask Mandates Unconstitutional!

ByTimothy Shea
11 June 2021


The tide is FINALLY starting to turn, as courts begin to address the myriad unconstitutional government infringements of our rights over the past year. The First District Court of Appeal in the State of Florida ruled today that the government can’t simply assert an “emergency” as a justification to violate our fundamental rights. The court further held that IF the government does indeed have a compelling interest in regulating behavior, courts must apply “strict scrutiny” to determine whether it has chosen the least-restrictive means possible to accomplish the desired result.

The case, Green v. Alachua County, was an appeal from a lower court ruling that denied Plaintiff Justin Green’s motion for a temporary injunction against the County to suspend enforcement of its mask mandate. The appellate court reversed the lower court ruling, saying that the trial court did not apply the correct legal standard of strict scrutiny to reach its decision.

In most circumstances, governments are given wide latitude and broad regulatory discretion, and courts will accord due deference to executive branch decisions about the extent of their authority to act, provided that there is “a reasonable, rational nexus” between the end sought and the action taken. However, whenever executive branch action impacts a fundamental right, the standard shifts from “reasonable, rational nexus” to “strict scrutiny” and the burden of proof shifts from the plaintiff alleging that his or her rights have been violated to the executive branch defendant to prove that it chose the least-restrictive means of achieving the desired objective.

Strict scrutiny entails a two-part test. First, does the government have a compelling interest in the regulation issued? An example of a compelling interest would be seizure and drainage of swampland that was a hazard to health, say by being a breeding ground for disease-carrying mosquitoes. Second, if the government meets the compelling interest test, did it select the narrowest, most targeted solution? In our swampland example, did the government seize the least amount of land? Were there other, less-restrictive alternatives, such as spraying insecticide? Or would spraying perhaps pose a bigger health risk than the mosquitoes? Courts frequently are called upon to conduct such balancing tests to arrive at the best solution for society at large.

In the instant case, the appeal court found that the trial court erred in two ways. First, it used the wrong case law and arrived at an incorrect legal conclusion as to whether the County had violated a fundamental right of Plaintiff Green’s and therefore placed the burden of proof on the wrong party. The Court of Appeal ruled that the correct legal analysis is that under the Florida Constitution, the right to privacy is fundamental and that the County’s mask mandate is presumed to be unconstitutional and that the County bears the burden of proving first that it had a compelling interest in issuing the mask mandate and second, that a mask mandate was the least restrictive means of satisfying that compelling interest. The appeal court further ruled that because the trial court had arrived at an incorrect conclusion about whether a fundamental right was involved, it applied the wrong legal standard of review.

Although written with dispassionate, sober language, any fair reading of this decision can only be described as a titanic smackdown of the trial court by the appeal court. (In fairness, this is because the appellate court had previously made the same mistake. The court even said as much in the decision, when it described the prior case and asserted, “We will not make that mistake again” with regard to assigning the burden of proof.) It reversed the trial court decision and remanded the case back for proper adjudication.

Although this was only a state-level case and not a Federal case, and despite the fact that the case will now likely be dismissed as moot by the trial court because Governor DeSantis has prohibited additional mask mandates in the state of Florida, the legal analysis presented by the appellate court here blazes a trail for lawyers in other cases in other states to follow. We have been told to expect similar rulings from around the nation on mask mandates and other issues as courts begin cleaning up messes that the federal and several state Executive Branches made in 2020.

Green-v-Alachua-County-Court-of-Appeal-OpinionDownload
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TammyinWI

Talk is cheap
Thank you, I have read that also. These people are so sick with their plans to depopulate the world. Many people are having a hard time accepting this. It is a great awakening.

You are welcome. I have a hard time wrapping my mind around it yet. Daily, I am like, "for real????" The audacity and pompous pride of these power-hungry luciferians is all...beyond surreal. They planned everything on a long continuum, including gmo foods and gmo cotton, think i.e. immune systems, and also: q-tips, covid test swabs, masks, and cotton dressings/bandages.

I have been connecting the dots re: the luciferian dragons and their plans for a long time, decades, and these "vaccines" are not in a "fourth clinical trial." It is beyond that, creating the fear and urgency in the masses and these "vaccines."

These were designed that way on purpose, they knew exactly what they were doing, for several years, leading up to this.

I hope and pray all of the luciferians lose their minds completely and all turn on each other. I pray and speak against "Operation Lockstep." Some of it is not going as the laid it out. God is in control. He is allowing this.

And the flu, where did it go???

I was sickened beyond belief of a video I saw of a hcp in scrubs smothering a frail man in a hospital bed, someone had recorded it with their phone, with a title of creating a covid death, or similar.
 

Heliobas Disciple

TB Fanatic
(fair use applies)

New Discovery Shows Human Cells Can Write RNA Sequences Into DNA – Challenges Central Principle in Biology
By Thomas Jefferson University June 12, 2021


DNA Change Concept

In a discovery that challenges long-held dogma in biology, researchers show that mammalian cells can convert RNA sequences back into DNA, a feat more common in viruses than eukaryotic cells.

Cells contain machinery that duplicates DNA into a new set that goes into a newly formed cell. That same class of machines, called polymerases, also build RNA messages, which are like notes copied from the central DNA repository of recipes, so they can be read more efficiently into proteins. But polymerases were thought to only work in one direction DNA into DNA or RNA. This prevents RNA messages from being rewritten back into the master recipe book of genomic DNA. Now, Thomas Jefferson University researchers provide the first evidence that RNA segments can be written back into DNA, which potentially challenges the central dogma in biology and could have wide implications affecting many fields of biology.

“This work opens the door to many other studies that will help us understand the significance of having a mechanism for converting RNA messages into DNA in our own cells,” says Richard Pomerantz, PhD, associate professor of biochemistry and molecular biology at Thomas Jefferson University. “The reality that a human polymerase can do this with high efficiency, raises many questions.” For example, this finding suggests that RNA messages can be used as templates for repairing or re-writing genomic DNA.

The work was published June 11th, 2021, in the journal Science Advances.

Together with first author Gurushankar Chandramouly and other collaborators, Dr. Pomerantz’s team started by investigating one very unusual polymerase, called polymerase theta. Of the 14 DNA polymerases in mammalian cells, only three do the bulk of the work of duplicating the entire genome to prepare for cell division. The remaining 11 are mostly involved in detecting and making repairs when there’s a break or error in the DNA strands. Polymerase theta repairs DNA, but is very error-prone and makes many errors or mutations. The researchers therefore noticed that some of polymerase theta’s “bad” qualities were ones it shared with another cellular machine, albeit one more common in viruses — the reverse transcriptase. Like Pol theta, HIV reverse transcriptase acts as a DNA polymerase, but can also bind RNA and read RNA back into a DNA strand.

In a series of elegant experiments, the researchers tested polymerase theta against the reverse transcriptase from HIV, which is one of the best studied of its kind. They showed that polymerase theta was capable of converting RNA messages into DNA, which it did as well as HIV reverse transcriptase, and that it actually did a better job than when duplicating DNA to DNA. Polymerase theta was more efficient and introduced fewer errors when using an RNA template to write new DNA messages, than when duplicating DNA into DNA, suggesting that this function could be its primary purpose in the cell.
The group collaborated with Dr. Xiaojiang S. Chen’s lab at USC and used x-ray crystallography to define the structure and found that this molecule was able to change shape in order to accommodate the more bulky RNA molecule — a feat unique among polymerases.

“Our research suggests that polymerase theta’s main function is to act as a reverse transcriptase,” says Dr. Pomerantz. “In healthy cells, the purpose of this molecule may be toward RNA-mediated DNA repair. In unhealthy cells, such as cancer cells, polymerase theta is highly expressed and promotes cancer cell growth and drug resistance. It will be exciting to further understand how polymerase theta’s activity on RNA contributes to DNA repair and cancer-cell proliferation.”
Reference: “Polθ reverse transcribes RNA and promotes RNA-templated DNA repair” by Gurushankar Chandramouly, Jiemin Zhao, Shane McDevitt, Timur Rusanov, Trung Hoang, Nikita Borisonnik, Taylor Treddinick, Felicia Wednesday Lopezcolorado, Tatiana Kent, Labiba A. Siddique, Joseph Mallon, Jacklyn Huhn, Zainab Shoda, Ekaterina Kashkina, Alessandra Brambati, Jeremy M. Stark, Xiaojiang S. Chen and Richard T. Pomerantz, 11 June 2021, Science Advances.
DOI: 10.1126/sciadv.abf1771

This research was supported by NIH grants 1R01GM130889-01 and 1R01GM137124-01, and R01CA197506 and R01CA240392. This research was also supported in part by a Tower Cancer Research Foundation grant. The authors report no conflicts of interest.
 

Zagdid

Veteran Member
HIV positive woman carried COVID-19 for 216 days, the virus mutated 32 times inside her body! | Health News | Zee News (india.com)

HIV positive woman carried COVID-19 for 216 days, the virus mutated 32 times inside her body!
Written By:
Zee Media Bureau Updated: Jun 07, 2021, 12:50 PM IST


Researchers in South Africa have reported a potentially dangerous case of a 36 year old HIV positive woman who had carried COVID-19 virus in her body for a staggering 216 days. The virus mutated more than 30 times in a period of six months inside her body.

New Delhi: Researchers in South Africa have reported a potentially dangerous case of a 36 year old HIV positive woman who had carried COVID-19 virus in her body for a staggering 216 days. The virus mutated more than 30 times in a period of six months inside her body.

The case was first reported in a not peer-reviewed medical journal medRxiv on June 3. According to the report, the woman contracted COVID-19 in September 2020. The virus accumulated 13 mutations to the spike protein and 19 other genetic shifts that could change the behaviour of the virus. Some of these mutations have been seen in variants of concern, such as the Alpha variant (first reported in the UK) and Beta variant (first reported in South Africa).

The woman whose identity is not revealed, was first diagnosed with HIV in 2006 and her immune system has been consistently weakening over time.

Though right now there is little research to establish that HIV-infected people are more prone to contracting COVID-19 and developing severe medical consequences but if more such cases are found in HIV positive people then they could become "a factory of variants for the whole world".

“While most people effectively clear Sars-CoV-2, there are several reports of prolonged infection in immunosuppressed individuals. We present a case of prolonged infection of greater than 6 months with shedding of high titter SARS-CoV-2 in an individual with advanced HIV and antiretroviral treatment failure,” an expert of the study said as quoted by the Hindustan Times.

According to the study's researchers immunocompromised patients can carry the virus much longer in their bodies.

This is a worrisome trend for both South Africa and India. While there are around 7.8 million people affected by HIV in the African country, India also has almost 1 million people with untreated HIV infections.
 

marsh

On TB every waking moment

CDC claims COVID-19 kills 'healthy young children' as doctors push back on vaccinating kids

Authorities should worry about worsening vaccine hesitancy by pushing low-risk kids to get jabbed, med school professors warn.

By Greg Piper
Updated: June 13, 2021 - 11:11am

The Centers for Disease Control and Prevention now claims that "healthy young children" can die from COVID-19. Marty Makary wants to see the evidence.

"In reviewing the medical literature and news reports, and in talking to pediatricians across the country, I am not aware of a single healthy child in the U.S. who has died of COVID-19 to date," the Johns Hopkins University professor of medicine and public health said Thursday.

Archived versions of the CDC's web page comparing COVID-19 and seasonal influenza show that it revised the "differences" in the section "People at High-Risk for Severe Illness" sometime between May 31 and June 8.

"The risk of complications for healthy children is higher for flu compared to COVID-19," the earlier version says. "However, infants and children with underlying medical conditions are at increased risk for both flu and COVID-19."

The new version flips the emphasis as well as adding a new claim. "Overall, COVID-19 seems to cause more serious illnesses in some people," it begins.

"For young children, especially children younger than 5 years old, the risk of serious complications is higher for flu compared with COVID-19. However, serious COVID-19 illness resulting in hospitalization and death can occur even in healthy young children."

Makary's article in MedPage Today, a clinical news publisher where he serves as editor in chief, pushes back on calls to vaccinate kids ages 0 to 12 without comorbidities. He also recommends parents avoid vaccinating children who have recovered from COVID-19 infections, continuing his argument that natural immunity is just as good if not better than vaccine immunity.

"The case to vaccinate kids is there, but it's not compelling right now," Makary wrote.

He's part of a movement of doctors at medical institutions around the world calling for far more cost-benefit analysis of COVID-19 vaccines for low-risk populations such as children.

Professors from UCLA's schools of medicine and public health, the University of Maryland's pharmacy school, Harvard Medical School, Texas A&M Medicine and Oregon Health & Sciences University signed an international letter to the Food and Drug Administration June 1, listing steps it should take before approving any vaccine beyond emergency use authorization (EUA).

Among them: "at least 2 years of follow-up" with participants from the original clinical trials and "substantial evidence of clinical effectiveness that outweighs harms in special populations" including infants, children, adolescents and recovered people.

The CDC did not respond to a request to provide the source of its new claim about healthy young children.

Even as the agency scheduled a meeting for June 18 to discuss higher-than-expected reports of heart inflammation in recipients of the two-dose Pfizer and Moderna vaccines, particularly men ages 16-24, a CDC doctor emphasized the reports were just preliminary.

Worsened vaccine hesitancy possible
Makary's Thursday article seems partly spurred by the CDC's claim about healthy young children, though he doesn't mention the agency's revised comparison page.

His Johns Hopkins research team partnered with healthcare data provider FAIR Health, which has about half of U.S. health insurance data, to study pediatric COVID-19 deaths. "We found that 100% of pediatric COVID-19 deaths were in children with a pre-existing condition," which strengthens the case for vaccinating kids with comorbidities.

The CDC also warned that unvaccinated children were at risk for multisystem inflammatory syndrome (MIS-C), with a higher risk for teens and adolescents.

Makary's article said the CDC's own data show that MIS-C overwhelmingly targets black and Latino children, "likely due to the disproportionate rates of childhood obesity and chronic conditions in these populations." While three dozen have died, the weekly rate of COVID-associated MIS-C is now at zero.

1623623966411.png

Makary didn't respond to a request from Just the News to respond to the overall guidance coming from the CDC on children and COVID and media narratives that promote vaccination for children regardless of their risk level.

The international letter to the FDA emphasized longstanding efficacy and safety differences in how younger and older people respond to medicines. "The ongoing phase 3 trials of COVID-19 vaccines ... largely (or wholly) excluded" infants, children and adolescents, among other critical groups.'

Other doctors have warned about unique considerations of mass vaccination for children.

Makary's Johns Hopkins colleague Stefan Baral argued against EUAs for COVID vaccines targeted to children in a short essay with the University of California San Francisco's Vinay Prasad and Carnegie Mellon University's Wesley Pegden.

Though trials are underway for children as young as six months old, "the rarity of severe covid-19 outcomes for children means that trials cannot demonstrate that the balance of the benefits of vaccination against the potential adverse effects are favorable to the children themselves," they wrote in the British Medical Journal last month.

Prasad in particular has highlighted vaccine hesitancy by socioeconomic status and race, and the trio emphasized that hesitancy could intensify because of "accelerated mass child vaccination" driven by school mandates and vaccine passports.

"The possibility that rare adverse events could emerge as the more durable public health legacy of an emergency use authorization for child covid-19 vaccines is much greater," they wrote.

Emory University's Jennie Lavine and Rustom Antia and Pennsylvania State University's Ottar Bjornstad warned that "vaccinating children would likely lead to lower infection rates but higher case fatality rates."

Writing in the BMJ shortly after Baral, Prasad and Pegden, the trio cited evidence that children are less susceptible to infection and transmission compared to adults. Vaccinating them provides a "marginal benefit in reducing the risk to others" and may actually be worse for children in the long run.

"Once most adults are vaccinated, circulation of SARS-CoV-2 may in fact be desirable, as it is likely to lead to primary infection early in life when disease is mild, followed by booster re-exposures throughout adulthood as transmission blocking immunity wanes but disease blocking immunity remains high," they wrote. "This would keep reinfections mild and immunity up to date."
 

marsh

On TB every waking moment

'Partners with the Chinese': Ex-DOD official says U.S is 'complicit' in COVID lab leak

The Pentagon knew the Wuhan Institute of Virology was not merely "a civilian operation, but that it was involved in Chinese biowarfare," said Stephen Bryen, founding director of the Defense Technology Security Administration.

Video on website 9:59 min

By Sophie Mann
Updated: June 12, 2021 - 10:48pm

Stephen Bryen, the founding director of the Pentagon's Defense Technology Security Administration, believes it's time for the U.S. to confront its own culpability in the COVID-19 pandemic — starting with tough questions about the Defense Department's funding of the Wuhan Institute of Virology, the Chinese lab now widely suspected as ground zero in the spread of the SARS-CoV-2 virus to humans.

Last month, Kentucky Republican Sen. Rand Paul grilled Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, on the origins of the SARS-CoV-2 virus, as well as U.S. funding that made its way to the WIV to support research on bat coronaviruses suspected of being exploited in gain of function experiments. Fauci categorically denied under oath any gain of function funding present or past by the National Institutes of Health, the NIAID's parent agency.

"t looks to me as if the U.S. is complicit, because we funded the research at the Chinese laboratory in Wuhan," Bryen told "Just the News AM" in a recent interview. "And we did it for many years."

Bryen cited not only NIH support for the WIV, but also funding from the Pentagon. "Believe it or not, the most money came from the Pentagon," he said. "And one wonders why we are doing this and what's going on here. But the fact of the matter is that we were partners with the Chinese."

Bryen, who was among an inner core of influential Cold War hawks in the Reagan-era DOD, believes the Pentagon understood full well that the Wuhan Institute of Virology was not merely "a civilian operation, but that it was involved in Chinese biowarfare and other activities." The lab has been previously documented as a part of China's biological warfare program.

"We had a very good idea of what the Chinese were doing," said Bryen, adding that elements of the U.S. intelligence community have been "warning strongly" about biowarfare for more than a decade "There have been special panels convened at the very highest level of the White House," he said. "What were we doing there?"

Answering his own question, Bryen submits that the U.S. was likely participating in this controversial research at the WIV in the expectation that it would yield valuable insight in dealing with potential future coronaviruses. He theorized that Chinese scientists were at the fore of this particular field, and American scientists, perhaps rightly, thought it important to understand and be a part of that research instead of passively observing from across the ocean.

In testimony before the Senate Appropriations Committee on May 26, Fauci pled ignorance about the influence of China's ruling Chinese Communist Party over that nation's scientific community. "I don't have enough insight into the Communist Party in China to know the interactions between them and the scientists, sir," Fauci told Lousiana Republican Sen. John Kennedy.

Bryen is highly skeptical of Fauci's claim of ignorance. "He's a grown-up," said Bryen. "He's a serious person. His agencies knew what they were doing."

Neither Fauci nor the NIH have responded to requests for comment on this article
 

marsh

On TB every waking moment

WATCH: 2018 Video Shows Wuhan Lab Partner Scheming On How To Make Money From A Pandemic.
wuhan

While speaking at a conference in 2018, Wuhan Institute of Virology and collaborator and gain-of-function advocate Dr. Ralph Baric advised attendees on how to “make money” in the next pandemic.

Baric – who’s attended conferences at the Wuhan Institute of Virology and is described by Wuhan’s “bat woman” Shi Zhengli as one of her “longtime collaborators” – made the comments at an April 2018 event hosted at the University of North Carolina Chapel Hill. Baric – who’s described lifting bans on gain-of-function research as “critical” – also provided the Wuhan lab with humanized mice to likely conduct the controversial form of research with SARS-like coronaviruses.

“Gain-of-function represents one of those approaches that is a crucial tool for public health preparedness and response,” Baric asserted in 2014 while lobbying against a moratorium on gain-of-function research.

Rumble video on website .37 min

During his 2018 speech “Imagining the Next Flu Pandemic – and Preventing it!” he presents a slide titled “Global Catastrophe: Opportunities Exist.” The slide outlines what type of stocks and industries surged during the Ebola outbreak, which he uses to extrapolate financial advice on how to “make money in the next pandemic.”

“I wanted to give you good news. There are winners out there, right? So if you ever want to be prepared and make money in the next pandemic, if that’s what you want to do, buy stock in Hazmat suit makers and protective clothing or companies that make antiviral drugs for that particular pandemic,” he notes.

Baric adds that the aforementioned sectors and stocks would “probably do pretty well” before highlighting that “there are actually mutual funds for pandemic preparedness.”

MUST READ: Fauci Privately Advised Obama Staffers to NOT Wear Masks: ‘Not Effective’.
“Some products do well. 1918 including masks, same thing today,” he advises.

Screen-Shot-2021-06-13-at-11.14.58-AM-800x408.png

SLIDE.

While speaking over the following slide – “Pandemics: Opportunity” – Baric posits that “pandemics really are times of opportunity.”

“There is an opportunity for people to have political gain, financial gain, and personal gain during times of social upheaval, and that will probably occur,” he adds.

Screen-Shot-2021-06-13-at-11.18.25-AM-800x408.png

SLIDE.

Watch:
Rumble video on website 1:29 min
 

marsh

On TB every waking moment

WATCH: Footage Reveals Live Bats In Wuhan Lab Despite Denials.
wuhan

Despite Wuhan Institute of Virology and its U.S. taxpayer-funded collaborators such as EcoHealth Alliance’s Peter Daszak insisting the controversial lab didn’t work with live bats, new footage reveals researchers working the animal.

The footage aired on Sharri Markson’s Sky News program and reveals bats in cages at the Wuhan Institute of Virology and researchers catching and feeding the mammal. In one instance, a bat is seen hanging off the hat of a researcher from the Wuhan lab.

The evidence follows Daszak – whose organization funneled money from Anthony Fauci’s National Institute of Allergy and Infectious Diseases to partner with the Wuhan Institute of Virology – insisting otherwise.

“This is a widely circulated conspiracy theory. This piece describes work I’m the lead on & labs I’ve collaborated w/ for 15 yrs. They DO NOT have live or dead bats in them,” Daszak, who also served as a World Health Organization (WHO) COVID-19 investigator, tweeted.

Watch:
Rimble video on website 2:19 min
 
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