CORONA Main Coronavirus thread

Heliobas Disciple

TB Fanatic
(fair use applies)

Comments of Dr. Geert Vanden Bossche on the White House Summit on the Future of COVID-19 Vaccines
By Geert Vanden Bossche
July 27, 2022

Fast-forward to 6:45 to hear Fauci and watch for as long as you can tolerate ...

This is disgusting. As someone who has dedicated 3 decades of his professional life to analyzing the shortcomings of our traditional vaccine approaches and proposing new concepts of harnessing our immune system against infectious and immune-mediated diseases, I can only say that this is beyond shameful - a true insult to science! What you're watching is a clear example of what happens when scientists panic and are unable to grasp the basics of the single biggest challenge in vaccine research: 'immune escape'. They regurgitate countless fancy ideas, none of which have worked in the past! Why not? Because none of them has taken into account the formidable evolutionary capacity of viruses when put under (suboptimal!) immune pressure or even considered the critical role of innate immunity other than its inflammatory components (so-called 'adjuvants').

This reminds me of my initial days at the B&M Gates Foundation (2008) when stacks of proposals on new vaccine approaches from the most prestigious research institutes on the globe awaited my evaluation for funding. I soon discovered that very few people on this planet understand how pathogens subvert the immune system. This has been well-illustrated by decades of disappointing HIV vaccine development: billions of dollars have been wasted on all kinds of sophisticated vaccine approaches that basically promote immune escape rather than control the virus. What Fauci and this panel are proposing is to repeat this stupid exercise and "invest" countless billions of taxpayer dollars - Industry will flourish while the state moves deeper into insolvency. The pan-CoV vaccine design they're proposing has it all: multiple antigens in mosaic, nanoparticles, VLPs, mRNA, lipids, ferritin, adenoviral vectors, inactivated or live attenuated virus or other antigen carriers, either delivered parenterally of via the mucosal route! Their 'the more, the better' approach allows for intellectual laziness and undermines true science.

So, what happened to all these prestigious proposals that were waiting for me at the B&M Gates Foundation? I spent a few weeks reading each of them (a few thousand pages) and ended up rejecting them all for lack of immunological rationale or infringement of immunological principles, unnecessary complexity, safety concerns, lack of characterization, lack of feasibility from a manufacturing and regulatory viewpoint etc. etc. They were examples of fancy technologies that made no biological sense (at least not to those with a somewhat deeper understanding of biology, in particular the biology of the pathogen, the host and their mutual interaction). I figured the foundation would fire me on the spot and send me back to where I came from... however, they didn't! Up until this day, I appreciate and respect my former boss for having listened to my detailed arguments. Back in those days, scientific debate was still conducted and encouraged, at least to some extent. Unfortunately these days are now clearly gone! Instead, megalomania and corruption of our prestigious scientific leadership are now dominating the scene. Technologies are embraced over basic biology. Corruption plagues Big Pharma as it's become no secret that Industry is merely focused on generating benefit for their shareholders at the expense of global health. Do I worry about this development? I do not. My only concern is for the tremendous backlash disruptive human intervention on our own immune systems will cause, well before these 'high society' scientists and leaders in industry have had the chance to implement any of their new vaccine concepts...

Best regards,

Geert

There is no greater impotence in all the world like knowing you are right and
that the wave of the world is wrong, yet the wave crashes upon you
.
- Norman Mailer​
 

Heliobas Disciple

TB Fanatic
(fair use applies)

They are desperately trying to make you believe the virus came from nature. No way.
It is 2.5 years later and two papers appear on the same day?!? Should you believe it? I do not. Neither does Robert Malone or Chris Martenson. Here's why.
Steve Kirsch
8 hr ago





Executive summary


Two studies were just published in a peer-reviewed journal on the same day:
  1. Spatial study: The Huanan Seafood Wholesale Market in Wuhan was the early epicenter of the COVID-19 pandemic
  2. Genomic study: The molecular epidemiology of multiple zoonotic origins of SARS-CoV-2
Their conclusion: SARS-CoV-2 came out of nature

My conclusion: it definitely was a lab leak.

Introduction

Here’s what you need to know:
  1. Kristian Andersen is an author of both papers. What a coincidence! He was on the original call with Fauci after the breakout and participated in the cover up to make it look like it came from nature.
  2. Kristian Andersen blocked Chris Martenson and then deleted all his tweets after Chris Martenson called him out. Is that how science works?
  3. Andersen initially told Fauci the virus was man made in an email on Feb 1, 2022 that you can see right here (at 19:00). He said it was inconsistent with evolutionary theory. Then there are redactions to the FOIA emails and then a week later, there is a paper on how the virus came from nature. Pretty hard to cover that one up. Chris Martenson did a great series on this. It’s really hard to believe this wasn’t from a lab if you take the time to watch Chris’s video. It is awesome. If you are short on time, watch from 19:00 for at least 2 minutes. It’s one of my favorite Chris Martenson videos ever and it is the best 2 minutes you’ll ever spend if you are wondering where the virus came from.
    The email where the virus was determined to be man-made by Kristian Andersen’s team (see 19:00). But a week later, it was of natural origin!!!
  4. Why now? Why didn’t we have this before? And the papers came out at the exact same day 2.5 years later? Just a coincidence. Sounds like a coordinated PR plan to me.
  5. How do we know the Chinese government didn’t manipulate the data on spread?
  6. Why did the Chinese government allow the data to be released all of a sudden?
  7. Li-Meng Yan said the virus was deliberately released from the lab. So how do we know they didn’t release it at the wet market to make it LOOK like it jumped from animals? It’s the perfect cover story. And all the cases reported would be consistent with a wet market origin since that is where it was released. The perfect crime.
  8. Why is there no explanation in the genomic study for the furin cleavage site (FCS) origin? It isn’t even mentioned. How could you not mention this at all? This is the smoking gun of gain of function (GoF) research. The FCS cannot be created in nature. So how do they explain it? They don’t! They completely side-stepped even mentioning it in the paper. WTF?!? But I guarantee you Kristian Andersen knows all about the FCS. Not mentioning it at all is a tacit admission that they cannot explain it. The problem they have is the FCS is a 19 nt sequence that is ONLY found in a 2015 Moderna patent. Now what do you think that the chances of a man-made sequence only found in a 2015 patent from the company charged with making a vaccine to the SAME virus and sequence just happens to match the genetic sequence that RANDOMLY was generated in nature? It is zero.
  9. There is nothing in the paper explaining why Kristian Andersen’s team rejected the man-made argument. They went from man-made to evolution in just 3 days without any data changing (watch the video for 2 minutes starting at 19:00)! Of course, there’s a reason for that. The reason is because Fauci asked him change the conclusion. The truth wouldn’t be appropriate to publish in a paper.
  10. What did Moderna say when asked about the FCS matching their 2015 patent application? They said, “Our scientists are looking into it.” Does the press ever follow up on that to see how it’s going? Of course not!
  11. Isn’t it a little too coincidental that Wuhan Institute of Virology (WIV) was working on GOF research on bat coronaviruses? FCS found in the virus would be consistent with that.
  12. The CEO of Moderna - Bancel - was also the ex-CEO of the company bioMerieux which helped build the Wuhan virology lab. What a coincidence that the 19 nt sequence from the Moderna patent ends up popping up just 11 miles from the lab that Bancel built. It has to be the greatest coincidence in human history.
  13. Comedian John Stewart figured this stuff out a year ago; why can’t Kristian Andersen? The official name of the lab isn’t what Stewart said, but people in China do call it the Coronavirus Research Lab in Wuhan (I checked with Li-Meng Yan).
  14. It’s fundamentally a bat virus, but bats aren’t sold at that market. Why
  15. There is a public paper trail including grant applications and very similar prior art in the public domain for GoF. If this didn’t come from a lab, it is the greatest coincidence of all time.
  16. If it originated in November 17 in Wuhan, then why were so many cases apparently discovered before that time?
  17. I sent Kristian an email asking if he was interested in entering a contest on debating the origin of the virus where he could win $1M. If he doesn’t reply, we’ll know he’s not very confident.
  18. How is is impossible that the origin of the virus is really the WIV (just 10 miles from the wet market) but it was released at the wet market to create a cover story. What is it about the genome that shows that it couldn’t have come from a lab? Kinda silent on that one. Why couldn’t the lab have made the genome to make it look like it came from animals?
  19. One explanation is that that lab workers took the animals from the Wuhan lab that were being disposed of and sold them in the Wuhan wet market for extra cash. Someone who lived in the area wrote a paper on this. Why was this possibility discarded?
  20. Look how close the wet market is to WIV and WIV: right across Yangtze river. It would be way too suspicious if released TOO close to the lab. Li-Meng said that they deliberately released it into the public so doing it at a wet market nearby, but not adjacent, provides the perfect cover story.


Do you want to know the reason it couldn’t have come from the lab? It’s because they have tight controls! Check this out (from Wuhan lab says there's no way coronavirus originated there. Here's the science):

Just today (April 18), the vice director of WIV Zhiming Yuan CGTN(opens in new tab), the Chinese state broadcaster, said "there is no way this virus came from us," NBC News reported(opens in new tab). "We have a strict regulatory regime and code of conduct of research, so we are confident."

(sarcasm on) Sure. That’s PROOF. There is no need to release the genetic sequences because the lab says they have a strict regulatory regime. Releasing the genome is completely unnecessary! No reason for the WHO committee to visit the lab. After all, if you can’t trust the WIV, who can you trust? (sarcasm off)

But this paragraph is critically important (pay attention to the part in bold):

WIV was not immune to those concerns. In 2018, after scientist diplomats from the U.S. embassy in Beijing visited the WIV, they were so concerned by the lack of safety and management at the lab that the diplomats sent two official warnings back to the U.S. One of the official cables, obtained by The Washington Post, suggested that the lab's work on bat coronaviruses with the potential for human transmission could risk causing a new SARS-like pandemic, Post columnist Josh Rogin wrote.

They were ordered to release it nearby so it could be “tested” to see if it worked. What better place than a food store that everyone visits.

And when the WHO scientists charged with investigating the leak wanted to access the WIV facilities to verify it didn’t come from the lab and get the genomic sequences of what the lab was working on, do you think they were invited with open arms and full access? No way.

The gene sequences are missing!

If Kristian Andersen were an honest scientist, he’d eliminate the WIV as a source by getting the genomic sequences of the coronaviruses that they were working on there.

Have you ever seen the genomic sequences of the coronaviruses being studied at WIV? I haven’t. You cannot find them it seems.

Wanna know why? It’s because the NIH deleted them from public access!

Check out this article: NIH Deleted Info From Wuhan Lab On Covid-19 Genetic Sequencing, Watchdog FOIA Finds

Why were they deleted? Well, because the Chinese asked them to, of course!

How convenient is that?

The data is still at NIH, but it is not publicly accessible.

Democrats in Congress don’t want to ask the NIH to release the data.

The reason is simple: it would show that the leak came from WIV. And that then leads back to the US government. That’s why the Democrats will not ask for the data: they don’t want any of to learn the truth.

Robert Malone isn’t buying it

Robert Malone isn’t buying the cover story.

Chris Martenson isn’t either

Chris responded to my email. Let’s just say that Chris was as unimpressed as I was. Here’s my paraphrase of the “essence” of what he told me.

It's all the same cast of shithead virologists. The conflicts of interest are legendary, the same ones one in Fauci's redacted emails are all over this publication, they never did ANY sequencing or genetics at all, and the rest, such as it is, is entirely circumstantial.
In short, be really careful what you see in the peer reviewed literature regarding COVID, especially if Kristian Andersen’s name is on the paper.

Please help support his channel. He just got a strike on YouTube so he can’t post for a week. His crime? He cited a paper in the peer reviewed literature. I’m surprised he wasn’t banned for life for that mistake!

Summary

I’m not buying the cover story. Neither are Malone or Martenson. And neither should you.

If you disagree with me, let’s settle the issue in front of an expert panel. If you win, you can get $1M. Details here.
 

Heliobas Disciple

TB Fanatic
(fair use applies)

Rewriting history: Just another day in DC
"Lab leak", "Wuhan wet market", "Devil's Hole", "Big Tom" and "Gain-of-Function" Research. War is peace. Fiction is truth. In short, a propaganda round up.
Robert W Malone MD, MS
19 hr ago

Not sure why Fauci continues to obfuscate about the origins of the virus… But we can all speculate why. It is nice to see Dr. Redfield not going for Fauci’s BS.

Former CDC Director Fires Back at Fauci’s ‘Natural’ Claim
The Epoch Times. July 26, 2022


(Read the whole story here)

“I’m disappointed in the [National Institutes of Health] for not leading an objective evaluation from the beginning,” Redfield (former director of the CDC) told the outlet. “I think it really is antithetical to the science where they took a very strong position that people like myself who are somehow conspiratorial just because we have a different scientific hypothesis.”
A reason why the Wuhan lab leak theory has not been fully recognized, Redfield argued, is due to the politicization of the pandemic response and the pressure that was heaped on scientists who sought objective approaches while studying the origins of COVID-19.
“I’ve been very disappointed in the scientific community led by [National Institutes of Health] that has really dug their heels in from the beginning to try to minimize any of us that have a different hypothesis,” he said.​

In contrast to what Redfield is saying above, right on time for election season, we now have a concerted propaganda push to craft the narrative that the US Government was not complicit in the development of SARS-CoV-2. Note that the conclusions are far from definitive- “Likely” according to the authors. This article in Science has been followed by a concerted PR push, which is often the best way to detect propaganda.

The molecular epidemiology of multiple zoonotic origins of SARS-CoV-2

Understanding the circumstances that lead to pandemics is important for their prevention. Here, we analyze the genomic diversity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) early in the coronavirus disease 2019 (COVID-19) pandemic. We show that SARS-CoV-2 genomic diversity before February 2020 likely comprised only two distinct viral lineages, denoted A and B. Phylodynamic rooting methods, coupled with epidemic simulations, reveal that these lineages were the result of at least two separate cross-species transmission events into humans. The first zoonotic transmission likely involved lineage B viruses around 18 November 2019 (23 October–8 December), while the separate introduction of lineage A likely occurred within weeks of this event. These findings indicate that it is unlikely that SARS-CoV-2 circulated widely in humans prior to November 2019 and define the narrow window between when SARS-CoV-2 first jumped into humans and when the first cases of COVID-19 were reported. As with other coronaviruses, SARS-CoV-2 emergence likely resulted from multiple zoonotic events.

From CNN (notice the wording - “New Studies Agree” (With whom? Fauci?):

New studies agree that animals sold at Wuhan market are most likely what started Covid-19 pandemic

And from Axios:

Wuhan market pinpointed as pandemic's Ground Zero


If you read these various articles, you will find that the actual text demonstrates that the issue is far from resolved.

Now, it isn’t like the USA doesn’t have a history of experimenting with biological and chemical weaponry… as long as it is legal, of course. So, when Dr. Fauci makes claims about the origin of the virus, it may be best to look to the past to see just what the USG has done in the past and is capable of doing.

So, here is some “old news,” that may be “new news” to most.

A 2002 CBS news articles on release of documents relating to the US bio-weapons testing during the 1960s is fascinating and more than a little scary. I have included the whole article - as I think that alerting Americans that such testing happened is very important. Mainly because I have no reason to suspect (insert sarcasm) that from time to time, they haven’t continued with such testing or had a surrogate (such as Israel) continue (as Israel has never signed the Biological weapons Convention).

CBS News - 2002

U.S. Admits Bio-Weapons Tests


The United States secretly tested chemical and biological weapons on American soil during the 1960s, newly declassified Pentagon reports show.
The tests included releasing deadly nerve agents in Alaska and spraying bacteria over Hawaii, according to the documents obtained Tuesday.
The United States also tested nerve agents in Canada and Britain in conjunction with those two countries, and biological and chemical weapons in at least two other states, Maryland and Florida.
The summaries of more than two dozen tests show that biological and chemical tests were much more widespread than the military has acknowledged previously.
The Pentagon released records earlier this year showing that chemical and biological agents had been sprayed on ships at sea. The military reimbursed ranchers and agreed to stop open-air nerve agent testing at its main chemical weapons center in the Utah desert after about 6,400 sheep died when nerve gas drifted away from the test range.
But the Pentagon never before has provided details of the Alaskan, Hawaiian, Canadian and British tests. The Defense Department planned to formally release summaries of 28 biological and chemical weapons tests at a House Veterans Affairs subcommittee hearing Wednesday.
The documents did not say whether any civilians had been exposed to the poisons. Military personnel exposed to weapons agents would have worn protective gear, the Pentagon says, although the gas masks and suits used at the time were far less sophisticated than those in use today.
The head of the House Veterans Affairs panel called for further investigation of the tests.
"Our focus must be on quickly identifying those veterans who were involved, assessing whether they suffered any negative health consequences and, if warranted, providing them with adequate health care and compensation for their service," said Rep. Chris Smith, a New Jersey Republican.
The tests were part of Project 112 (see more about Project 112 below), a military program in the 1960s and 1970s to test chemical and biological weapons and defenses against them. Parts of the testing program done on Navy ships were called Project SHAD, or Shipboard Hazard and Defense.
The United States scrapped its biological weapons program in the late 1960s and agreed in a 1997 treaty to destroy all of its chemical weapons.
Some of those involved in the tests say they now suffer health problems linked to their exposure to dangerous chemicals and germs. They are pressing the Veterans Affairs Department to compensate them.
Earlier this year, the Defense Department acknowledged for the first time that some of the 1960s tests used real chemical and biological weapons, not just benign stand-ins.
The Defense Department has identified nearly 3,000 soldiers involved in tests disclosed earlier, but the VA has sent letters to fewer than half of them. VA and Pentagon officials acknowledged at a July hearing that finding the soldiers has been difficult.
The tests described in the latest Pentagon documents include:
  • Devil Hole I, designed to test how sarin gas would disperse after being released in artillery shells and rockets in aspen and spruce forests. The tests occurred in the summer of 1965 at the Gerstle River test site near Fort Greeley, Alaska. Sarin is a powerful nerve gas that causes a choking, thrashing death. The Bush administration says it is part of Iraq's chemical arsenal.
    • Devil Hole II, which tested how the nerve agent VX behaved when dispersed with artillery shells. The test at the Gerstle River site in Alaska also included mannequins in military uniforms and military trucks. VX is one of the deadliest nerve agents known and is persistent in the environment because it is a sticky liquid that evaporates slowly. Iraq has acknowledged making tons of VX.
    • Big Tom, a 1965 test that included spraying bacteria over the Hawaiian island of Oahu to simulate a biological attack on an island compound, and to develop tactics for such an attack. The test used Bacillus globigii, a bacterium believed at the time to be harmless. Researchers later discovered the bacterium, a relative of the one that causes anthrax, could cause infections in people with weakened immune systems.
    • Rapid Tan I, II, and III, a series of tests in 1967 and 1968 in England and Canada. The tests used sarin and VX, as well as the nerve agents tabun and soman, at the British chemical weapons facility in Porton Down, England. Tests at the Suffield Defence Research Establishment in Ralston, Canada, included tabun and soman, the records show.
Tabun and soman are chemically related to sarin and produce similar effects.

Going further down this rabbit hole:

Project 112

Project 112 was a biological and chemical weapon experimentation project conducted by the United States Department of Defense from 1962 to 1973. The project started under John F. Kennedy's administration, and was authorized by his Secretary of Defense Robert McNamara, as part of a total review of the US military. The name refers to its number in the 150 review process. Every branch of the armed services and CIA contributed funding and staff. Canada and the United Kingdom also participated in some Project 112 activities.
Project 112 primarily concerned the use of aerosols to disseminate biological and chemical agents that could produce "controlled temporary incapacitation" (CTI). The test program would be conducted on a large scale at "extracontinental test sites" in the Central and South Pacific and Alaska in conjunction with Britain, Canada and Australia. At least 50 trials were conducted; of these at least 18 tests involved simulants of biological agents (BG), and at least 14 involved chemical agents including sarin and VX, but also tear gas and other simulants. Test sites included Porton Down (UK), Ralston (Canada) and at least 13 US warships; the shipborne trials were collectively known as Shipboard Hazard and Defense—SHAD. The project was coordinated from Deseret Test Center, Utah. As of 2015, publicly available information remains incomplete.

And there you have it folks.

Is there a reason we “should” trust Dr. Fauci when he now claims that he believes that the origin of the virus were natural? Is there some reason why the Democratically controlled Congress seems in no hurry to investigate the origins of the COVID virus?

Kudos to the Republican in the Senate and the Congress who have started such investigations last year. A June 29, 2021 Select Subcommittee Republicans Expert Witness Forum on COVID-19 Origins is just a start and I believe that a full investigation into the origins of this virus is only possible if the Senate turns red in November.

However, a letter penned by Senator Mike Gallagher for the purpose of this subcommittee investigation has some very interesting ideas on how to begin these investigations. From his letter:


There are a number of steps we can immediately take to better understand the origins of the virus so that we can prevent a similar crisis from happening again. These include:
• Declassifying all intelligence products, reporting, and assessments relating to COVID-19 origins and in particular those underpinning the IC assessments related to President Biden’s May 26, 2021 directive on a COVID investigation, the January 2021 State Department disclosures, and the material used to inform the April 30, 2020 DNI statement on COVID origins.
• Issuing a subpoena to the EcoHealth Alliance for any and all data and files they have relating to their collaboration with the Wuhan Institute of Virology.
• Auditing the records of all federal agencies for a thorough accounting of any funding that may have gone to the Wuhan Institute of Virology either directly or through third parties such as NGOs over the past decade.
• Continuing the State Department’s Arms Control Investigation into potential biological weapons convention violations.

A year later, and one must wonder how many of these suggestions have been taken up by Congress and the administrative state?

Where are those old school main-stream media type reporters when you need them?

And then we have the House Select Subcommittee on the Coronavirus Crisis. The official propaganda outlet for the Administrative State on all things relating to the COVIDcrisis. Right on time. Honest, it’s all Trump’s Fault!! No-one in the Administrative State has any guilt, the bad Trump people made us do it!

(Notice the unwritten subtext behind this - tacit acknowledgment that this whole mess was grossly mismanaged from a public health perspective. Probably because the response was not really about public health?)

Let’s take a look at an example of their work product. Talk about Mass Formation Psychosis!





New Select Subcommittee Report Reveals Full Scope Of Trump Administration’s Embrace Of A Dangerous And Discredited Herd Immunity Via Mass Infection Strategy

Report is the first in a series on the Select Subcommittee’s investigation into the Trump Administration’s political interference with the federal coronavirus response

Let’s examine this propaganda piece section by section:


Washington, D.C. (June 21, 2022) – Today, the Select Subcommittee on the Coronavirus Crisis, chaired by Rep. James E. Clyburn, released a staff report revealing new evidence of the far-reaching support for a dangerous and discredited herd immunity via mass infection strategy inside the Trump White House. The embrace of this strategy enabled Trump Administration officials to justify forgoing meaningful action to curb the spread of the virus when no vaccines were available and treatments were limited, likely contributing to many preventable deaths in the fall and winter of 2020-2021.

Well, well. Acknowledgment and validation that there were many preventable deaths in the fall and winter of 2020-2021. Of course nothing here to see regarding the preventable deaths caused by the vaccine. But it was all the fault of “Trump Administration Officials”, who failed to provide “meaningful action to curb the spread of the virus when no vaccines were available and treatments were limited”. Keep in mind that it was administrative state hacks like Rick Bright and Janet Woodcock who conspired to prevent Americans from accessing early treatment using repurposed drugs by circumventing the will of the POTUS.

[continued next post]
 

Heliobas Disciple

TB Fanatic
[continued from post above]

See for example:

DR ZELENKO EXPOSES HOW DR RICK BRIGHT'S VERY BAD MOVE SABOTAGED EARLY COVID TREATMENT KILLING MASSES

Moving on… The misrepresentations are continuous.

“The Select Subcommittee’s investigation has revealed extensive evidence of the Trump Administration’s efforts to undermine the nation’s public health response to the coronavirus crisis in an attempt to benefit the former president politically. As today’s report makes clear, senior officials in the previous Administration embraced a dangerous and discredited herd immunity via mass infection strategy promoted by non-expert advisers like Dr. Scott Atlas and recklessly allowed the coronavirus to infect Americans before vaccines were widely available.
This dereliction of duty resulted in significant loss of life that could have been prevented. We must honor those we’ve lost by bringing this shameful recent history to light and ensuring that it is never repeated—politics must never again be prioritized over the health and lives of the American people.”

So I guess that Scott Atlas is to be the fall guy to cover up the fact that Deborah Birx, Tony Fauci and their intelligence community buddies forced the US Government and the WHO to implement strategies based on CCP propaganda?

For more on this, see

Send in the HHS clowns. Why Public Health Officials running the COVID-circus have failed our country

The Press Release continues..

Today’s staff report, titled, “The ‘Atlas Dogma’: The Trump Administration’s Embrace of a Dangerous and Discredited Herd Immunity via Mass Infection Strategy,” is available in full here and reveals the following key findings:
Outspoken Proponents of a Dangerous and Discredited Herd Immunity Strategy Attempted to Influence the Trump Administration’s Pandemic Response from the Earliest Months of the Coronavirus Crisis
  • During a transcribed interview, White House Coronavirus Response Coordinator Dr. Deborah Birx revealed to the Select Subcommittee that Dr. Scott Atlas’s “influence began much earlier than his July 2020 arrival into the White House” when he formally became a Special Advisor to the President. For instance, an email released for the first time today shows that Dr. Atlas contacted Centers for Medicare & Medicaid Services Administrator Seema Verma on March 21, 2020, arguing that the federal government’s pandemic response was “a massive overreaction” that was “inciting irrational fear” in Americans. In the email, Dr. Atlas incorrectly estimated that the coronavirus “would cause about 10,000 deaths”—which he wrote was comparable to the toll from a normal flu season and “would be unnoticed”—and said, “The panic needs to be stopped.”

The truth is that at this point, we have no idea how many US deaths were actually due to the coronavirus because of the perverse financial incentives provided by HHS to hospitals and medical care providers, and grossly inappropriate use of PCR assays. The official mortality count attributed to the virus by the HHS is among the highest in the world. Many emerging economies have population adjusted mortality rates which are aligned with the Scott Atlas scenario. Haiti, which population chronically takes Chloroquine to prevent Malaria, has one of the lowest mortality rates in the world.
Likewise the African Malaria belt countries.

Jared Kushner Secretively Hired Dr. Atlas in July 2020 and Initially Concealed His Role Before Dr. Atlas Received Sweeping Access to Top White House Officials
  • New evidence obtained by the Select Subcommittee shows that White House Senior Adviser Jared Kushner initially took steps to conceal Dr. Atlas’s July 2020 hiring for several weeks. For instance, Dr. Atlas informed the Select Subcommittee in a transcribed interview that Mr. Kushner instructed him not to announce himself on conference calls and directed him to hide his White House identification card in his briefcase before first meeting with Dr. Birx.
    • Later, Dr. Atlas was given an office in the White House and was granted extensive access to the highest levels of government. According to Centers for Disease Control and Prevention (CDC) Director Dr. Robert Redfield, Dr. Atlas “had the ear” of the president on pandemic policy. Confirming prior reports, Dr. Birx told the Select Subcommittee that she believed President Trump received “parallel data streams” from Dr. Atlas that differed from the data provided by the White House Coronavirus Task Force, and that this information influenced President Trump to downplay the severity of the virus and reject many mainstream mitigation measures. Mr. Kushner also included Dr. Atlas in a series of meetings referred to as “China Virus Huddles,” which were attended by an exclusive group of President Trump’s inner circle.

And so, if you cut through the breathless hyperbole, Kushner brought in someone who disagreed with Fauci, Birx and Redfield. We already know, by Birx’ own admission in her book, that Birx and Redfield were actively overruling the guidance and advice of seasoned CDC personnel, and doing so without consultation with others.

To my eye, it appears that Kushner was doing precisely what he should have been doing- getting a second opinion!

Dr. Atlas Successfully Pressed the Trump Administration to Weaken CDC’s Coronavirus Testing Guidance, Resulting in a Reduction of Tests

New evidence obtained by the Select Subcommittee shows that Dr. Atlas set in motion significant changes to CDC’s testing guidance within days of arriving in the White House. On August 3, 2020, Dr. Atlas prepared a memorandum titled “Specific Notes on Prioritized Testing,” which claimed that it was “harmful to do massive testing,” and argued that “people have been convinced that ‘testing, testing, testing’ is urgent for everyone—that is false.”

In retrospect, as far as I am concerned, Atlas was the voice of reason here.

Director Redfield revealed in a transcribed interview that “significant people” inside the Trump Administration made clear shortly after Dr. Atlas arrived that “there needed to be some curtailment of the amount of testing that was done.” Director Redfield and other Trump Administration officials told the Select Subcommittee that Dr. Atlas spearheaded changes to CDC’s testing guidance made on August 24, 2020, which resulted in CDC no longer recommending that all close contacts of individuals infected with coronavirus get tested. A recommendation that such individuals isolate for 14 days, after being included in a draft, was also deleted before publication.
Dr. Atlas became enraged after CDC, on September 18, 2020, restored its original recommendation that all close contacts get tested. Director Redfield told the Select Subcommittee that Dr. Atlas “aggressively spoke to me in loud terms” and accused him of not having the approval to make the changes. HHS Assistant Secretary for Health Admiral Brett Giroir, the Trump Administration’s “Testing Czar,” told the Select Subcommittee that he recognized the potential that “somebody wanted to fire me” for his involvement in restoring the original testing recommendation.

Again, please keep in mind that by Birx’ own admission, she worked directly with Redfield to re-write and circumvent the recommendations that the CDC were providing. Again, in retrospect, as we have seen in so many other countries, mass testing and contact tracing were not useful in curtailing the spread of this highly infectious respiratory virus.

As to Giroir, he had been previously fired from his appointment in Texas, largely because he acted like an arrogant jerk.

Dr. Birx told the Select Subcommittee that the August 24, 2020, guidance ultimately resulted in a “dramatic decline of the number of tests performed during the end of August and the beginning of September.” In a September 16, 2020, email obtained by the Select Subcommittee, Dr. Atlas acknowledged to other senior White House officials that testing had decreased, but argued that “pushing more testing is destructive to opening” and proposed a further “ACTION” calling to make PCR tests less sensitive.

Which is to say that Atlas sought to make the PCR tests more specific. That is the way testing works - one has to choose between sensitivity and specificity. What a load of bollox. It is now widely acknowledged all over the world that the PCR testing cycle number policies resulted in a huge number of false positives, which of course was to the benefit of the hospitals and health care providers who were financially incentivized to over-diagnose COVID.

Dr. Atlas Advanced His Dangerous and Discredited Herd Immunity Strategy Within the Trump Administration
  • The Select Subcommittee’s investigation uncovered internal memoranda used by Dr. Atlas to push the Trump Administration to jettison proven mitigation measures and deliberately reduce testing—months before the first coronavirus vaccines were available to the public. One undated memorandum criticized the pandemic response strategy advocated by mainstream public health officials and argued: “Stopping all cases is not necessary, nor is it possible. It instills irrational fear into the public.” The memorandum also argued that widespread testing “sets up an unattainable goal that is harming this president.”
What can I say. Scott Atlas was correct. The history of the CORONAcrisis clearly demonstrates this. And Scott Atlas had a mission which included protecting the POTUS. Seems to me that he was just doing his job.

  • In a newly released email to senior White House officials on October 4, 2020, Dr. Atlas mocked then-candidate Joe Biden’s embrace of then-prevailing public health practices, writing: “Joe Biden’s policy is mask mandates and lockdowns. That is also the CNN and MSNBC attack narrative.” Dr. Atlas falsely told the senior White House officials that “the research studies, the best data, indicates that general masks are not effective.”

Oh, please. Give me a break. This is pure propaganda. The masks do not work. There are so, so many studies now. Furthermore, there are three main routes of infection by the virus. Mouth, nose and eyes. Cloth or paper dust masks do not protect your eyes, last time I checked.
  • Dr. Atlas also used his newfound position of power to recruit herd immunity proponents to meet with multiple senior Administration officials, including President Trump, Vice President Pence, and Secretary Azar. Director Redfield said that Dr. Atlas arranged these meetings “to convince people that herd immunity was going to save us, and this thing was going to go bye-bye.” Following one of these meetings, Secretary Azar tweeted that the herd immunity proponents provided “strong reinforcement” of the Trump Administration’s ongoing response strategy.

Yes, we have heard from these dastardly “herd immunity advocates” who were pushing “dangerous” ideas such as those of the Great Barrington Declaration. Which Fauci and the administrative state did everything that they could to discredit. But they were right. Early treatment should have been made widely available and should have been particularly focused on the high risk populations. Likewise, when the (rushed) vaccine products became available, they should have been focused on the highest risk populations rather than the general population. If these had been the policies, we probably would have long been over this whole CORONAcrisis and the ensuing massive economic and other collateral damage and preventable loss of life.

Top Trump Administration Officials Ignored Multiple Warnings and Embraced Dr. Atlas’s Herd Immunity Strategy, Resulting in Preventable Illness and Death
Dr. Atlas told the Select Subcommittee that White House Chief of Staff Mark Meadows, Assistant to the President Hope Hicks, Chief of Staff to the Vice President Marc Short, and HHS Deputy Chief of Staff Paul Mango, among others, came to support at least some of the pandemic policy views he was urging the Administration to adopt. He also said that he inferred that President Trump “was in agreement” with his views on the pandemic, given President Trump’s “own words.”

Uh, yeah, because Scott Atlas was the objective grownup in the room. It is to their credit that these staffers listened to him instead of Debora Birx, who was parroting CCP propaganda and policies which resulted in massive damage to virtually all of the western nations.

Director Redfield said that Dr. Atlas “successfully got a lot of people within the Task Force and the White House to believe that all we had to do was get to herd immunity” in order to contain the virus. Dr. Birx similarly said that Dr. Atlas’s herd immunity approach gained steam inside the White House throughout the fall of 2020. Doctors on the Task Force said they raised their concerns with Vice President Pence, Mr. Kushner, and Mr. Short, but no action was taken.
With Dr. Atlas’s influence fully entrenched, the Trump White House made little attempt to curb the spread of the coronavirus in the fall and winter of 2020 and early 2021—even as outbreaks surged across the country. With Dr. Atlas providing a veneer of scientific backing to justify inaction, the Trump Administration instead focused on downplaying the threat of the virus leading up to the November presidential election and on advancing the Big Lie in the weeks that followed. Dr. Birx informed the Select Subcommittee that, in her view, more than 130,000 American lives could have been saved after the first wave of the pandemic if President Trump and his Administration had implemented “optimal mitigation across this country.”

How many lives were lost due to the conspiracy of the Administrative State, working with Birx, Fauci, Redfield et al to suppress availability of early treatment using existing licensed drugs? Hard to say, because the overall mortality figures were grossly overinflated due to the PCR testing set points resulting in poorly specificity, together with the perverse financial incentives to designate all persons hospitalized or dead who were “PCR positive” as deaths due to COVID.

But the record clearly demonstrates that the real sin here was the active suppression of early treatment by the HHS Administrative State and its leading bureaucrats. Greater than 90% of deaths actually attributable to COVID were probably preventable.

And that is the real “Big Lie”.

The history of the Omicron infection waves and the data from all over the world (previously summarized here) validate Dr. Scott Atlas and his actions. My interpretation of all of this is that Dr. Atlas came to DC in an earnest attempt to serve his nation, and he ran into the nest of vipers which have come to run the entire HHS system. His primary sin was being naive about the viper pit that he was stepping into, but it was not that he made the wrong calls during the heat of battle. In my opinion, he deserves a Purple heart for his service, not vilification by a bunch of self serving wankers and propagandistic spin meisters.

I am often asked whether Fauci, Birx, Woodcock, Peter Marks, Rochelle Walensky and that whole crowd will ever come clean. Will they ever admit their mistakes?

Hell no.

They will just double down in their efforts to hide their complicity in destroying our economy, the legitimacy of the entire HHS enterprise, bioethics, clinical research and regulatory affairs norms, hiding the toxicity of the genetic vaccines, and compromising the education and health of our children.

The only remedy will be at the ballot box. God help us all.
 

Heliobas Disciple

TB Fanatic
(fair use applies)

Former CDC Director Fires Back at Fauci’s ‘Natural’ Claim
By Jack Phillips
July 26, 2022

Former Centers for Disease Control and Prevention (CDC) Director Robert Redfield rejected White House adviser Anthony Fauci’s claims that it’s more likely COVID-19 originated naturally.

In a recent interview, Fauci said he has an “open mind” but still believes that the virus occurred naturally after previously dismissing the theory that it emerged from the Wuhan Institute of Virology in late 2019. “It looks very much like this was a natural occurrence, but you keep an open mind,” Fauci said.

When asked about Fauci’s recent comments on Monday, Redfield told Fox News that he still suspects COVID-19 emerged “from the laboratory” and “had to be educated in the laboratory to gain the efficient human-to-human transmission capability that it has.”

“There’s very little evidence, if you really want to be critical, to support” the natural emergence theory, he said. The former Trump administration official then compared COVID-19 to prior coronaviruses such as Middle Eastern Respiratory Syndrome (MERS) and Severe Acute Respiratory Syndrome (SARS) that emerged about 10 years ago, saying that neither virus had the same transmission capacity as COVID-19.

“So it’s really exceptional that this virus is one of the most infectious viruses for man. And I still argue that’s because it was educated how to infect human tissue,” Redfield told Fox News.

Laboratory

The same Wuhan laboratory, he added, was the subject of a 2014 report amid claims that researchers performed research on bat-borne viruses that could impact humans.

“I’m disappointed in the [National Institutes of Health] for not leading an objective evaluation from the beginning,” Redfield told the outlet. “I think it really is antithetical to the science where they took a very strong position that people like myself who are somehow conspiratorial just because we have a different scientific hypothesis.”

A reason why the Wuhan lab leak theory has not been fully recognized, Redfield argued, is due to the politicization of the pandemic response and the pressure that was heaped on scientists who sought objective approaches while studying the origins of COVID-19.

“I’ve been very disappointed in the scientific community led by [National Institutes of Health] that has really dug their heels in from the beginning to try to minimize any of us that have a different hypothesis,” he said.

Both the NIH and Fauci have come under scrutiny over the agency’s decision to provide hundreds of thousands of dollars to a third-party group to assist in researching bat coronaviruses at the Wuhan lab.

After spending years working at the NIH, Redfield was named by former President Donald Trump to head the CDC in March 2018. He stepped down at the end of Trump’s term in January 2021.
 

Heliobas Disciple

TB Fanatic
View: https://www.youtube.com/watch?v=NUS15lyMqKQ
Spike Damages The Heart Muscle Through Innate Immune Arm Activation (Study)
37 min 49 sec
Streamed live 4 hours ago
Drbeen Medical Lectures

A study presented at American Heart Association's conference demonstrates for the first time how spike protein directly damages heart tissue without binding to ACE2. Let's review.

URL list from Wednesday, Jul. 27 2022

Coronavirus spike protein activated natural immune response, damaged heart muscle cells | American Heart Association
https://newsroom.heart.org/news/coron...

BCVS Scientific Sessions 2022 - Professional Heart Daily | American Heart Association
https://professional.heart.org/en/mee...

American Heart Association Financial Information | American Heart Association
https://www.heart.org/en/about-us/aha...

Study shows heart damage linked to COVID | FOX21 News Colorado
https://www.fox21news.com/news/study-...

Researchers Discover How COVID-19 Damages Heart
https://www.webmd.com/lung/news/20220...

Zhiqiang LIN | Boston Children's Hospital, MA | Cardiology
https://www.researchgate.net/profile/...

Toll-like receptor 4 - Wikipedia
https://en.wikipedia.org/wiki/Toll-li...
 

MinnesotaSmith

Membership Revoked
Original place I found this:


The Unvaxxed Will Inherit the Earth

"Strong evidence that the unvaccinated are more fertile than the vaccinated.
Interesting news on the birth rate drop front! It turns out that the highest vaccinated counties of Hungary have the worst drop in birth rates in 2022! This is a within-country comparison, comparing Hungarians to Hungarians, for the same time period.
You can see that the five least vaccinated counties experienced only a 4.66% drop in birth rates between Q1 of 2021 and Q1 of 2022. At the same time, five most vaccinated counties experienced a 15.2% drop in birth rates!
This is a tremendous 10.5% difference between birth rate outcomes! Put in other words, the birth rate decline in most heavily vaccinated Hungarian counties was THREE TIMES greater than the decline in least-vaccinated counties!
This is evidence, not conclusive proof, but the conclusive proof should not be long in arriving."
Posted on July 27, 2022 by VD

====================================================================


Hungary: Highest Vaccinated Counties Have Worst Birth Rate Drops!
Budapest is the new Taiwan -- Birth Rate Drop of -22.2%!

Igor Chudov
Jul 3
463
607

Interesting news on the birth rate drop front! It turns out that the highest vaccinated counties of Hungary have the worst drop in birth rates in 2022! This is a within-country comparison, comparing Hungarians to Hungarians, for the same time period.
Thanks to my incredible reader “handyman” and Twitter user @overcatbe, I came across two pieces of data:
I took my time to prepare a map of Hungary with vaccination data as of Jul 13, 2021, with birth rate changes overlaid and listed as BLUE (for declines) or RED (for increases).

Unfortunately, this data is noisy, as it presents only a single-moment snapshot of vaccination rates, and they are not super dissimilar. To make the comparison less noisy, I decided to pick five MOST vaccinated counties, and five LEAST vaccinated counties. The idea is to compare changes in birth rates among the most divergent counties, eliminating some amount of noise, driven by little-different counties.
Before I go further, I have to remind my readers: birth rates are always seasonal! Most parents prefer to make a “spring baby”, which often ends up with them making a “summer baby” because conception takes more time than expected. So, never compare adjacent quarters as they are guaranteed to have dramatic changes that are simply seasonality-driven, with differences very repeatable over the years. Only compare quarters of one year with same quarters of another year, please.
My own birth rate comparison compares Q1 of 2022, against Q1 of 2021. Since they are within-country comparisons, we can be more confident that they are driven by vaccination rates, as opposed to political, economic, or ethnic differences. These people are all Hungarians.
So, here are the 5 most vaccinated counties, contrasted with the 5 least vaccinated counties.

You can see that the five least vaccinated counties experienced only a 4.66% drop in birth rates between Q1 of 2021 and Q1 of 2022. At the same time, five most vaccinated counties experienced a 15.2% drop in birth rates!
NOTE: birth rate decline numbers are averaged without weighing by population. Our astute reader Richard Zucker commented and calculated the decline based on the number of total births for the most-vaccinated group and it is -17.4%, an even more impressive drop. The drop in the least vaccinated counties was 4.58%, a slightly lower number. So, on a population-weighted basis, the difference is 2% greater!
This is a tremendous 10.5% difference between birth rate outcomes! Put in other words, the birth rate decline in most heavily vaccinated Hungarian counties was THREE TIMES greater than the decline in least-vaccinated counties!
This is an apples-to-apples, Hungarians-to-Hungarians, same time period comparison! Pretty much the only variable is the extent to which those counties vaccinated their citizens by July 2021, including young people likely to make babies. Again, to remind you: the vaccination rates are a snapshot for July 13, 2021. You can add 9 months to July 2021, which gives you April 2022. Thus, you can see why birth rates in Q1 2022 changed: because of Covid vaccination.
The result? The more vaccination, the greater the declines in the birth rates.
Linear Regression


I ran a linear regression of the 20 county data pairs (vaccination rate on Jul 13 2021 vs birth rate drop in 2022). Here’s the result:

And here are the parameters of the straight line that the regression fitted (the trend line):


What is important is that statistical analysis shows the slope to be “statistically significantly different from zero”, in other words, the effect of vaccination on birth rate is highly likely NOT a fluke.
Another thing that is notable is that the “R-squared” — the measure of how much variation is explained by vaccination rate — is relatively low at 0.23. This is totally understandable, as we only have entire-population vaccination rates as of one specific date. There is no reason that the snapshot of somewhat unrelated numbers (vaccination rates including octogenarians) as of that date could explain the entire variation. But, sadly, this is the data that we have to work with. And it shows what we need to know: more COVID vaccines — fewer births.
Q.E.D.
For more interesting news regarding drops in birth rates this year, see my series:
Questions


Here’s a good looking Hungarian parliamentarian asking questions about what happened to her country:


Will Fertility Come Back?


It is becoming fairly apparent that the 2022 fertility drops are the true “black swans” of demographics, unprecedented in the breadth of countries involved, very large, deepening, extremely statistically significant, and very worrying.
A big question of the day is: is this a temporary situation or will the declines be permanent? If they are permanent, it may lead to depopulation of affected countries!
The answer is UNKNOWN to me and is also unknown to anyone else. Beware of vaccine advocates saying “birth rate declines are temporary and no big deal, the vaccine is working as expected”. Beware of vaccine skeptics jumping the gun and proclaiming that we will for sure be depopulated. We genuinely do NOT know, yet. The time has not passed yet, for us to know.
Despite not knowing, we can start worrying right now.
From other articles, we know that
  • Disruptions in female periods after vaccination are permanent in some women and temporary in others, proportions unknown
  • The decline in sperm quality seems to be permanent, with a minor rebound around 6 months, and that did not even consider booster doses
  • Further vaccination past July or so was extremely extensive, including booster vaccination of young fertile people, possibly further damaging their fertility.
I would, naturally, greatly prefer this problem be of temporary nature, even though I fear that it will not be.
Dear readers: do you think that we are dealing with a temporary decline, or a permanent decline? Please comment and explain your opinion.
 

BUBBAHOTEPT

Veteran Member
Rewriting history: Just another day in DC
:shk:
Good special on the Blaze from Tuesday night, concerning everything above. They bring all the receipts folks. However, as with last number of years, the evil is in DC. I think I’m beginning to understand why Christ went off the chain at the Temple. I wonder what he would do in DC.…:kaid:
 

Zoner

Veteran Member
So the news out of this latest geert video is that those who got vaccinated later may be a little better off because their natural immune system already was trained to fight the virus but he is still holding to his belief that covid is heading for a very deadly stage and fairly soon.
 

Heliobas Disciple

TB Fanatic
(fair use applies)

Los Angeles County avoids new mask rule as COVID stabilizes
CHRISTOPHER WEBER
Thu, July 28, 2022, 5:22 PM

LOS ANGELES (AP) — Los Angeles County dropped a plan to impose a universal indoor mask mandate this week as COVID-19 infections and rates of hospitalizations have stabilized, a top health official said Thursday.

Health director Barbara Ferrer said two weeks ago that the nation’s most populous county could again require face coverings if trends in hospital admissions continued under criteria set by the U.S. Centers for Disease Control and Prevention.

On Thursday, she said the county managed to dodge imposition of the broad mask rule. The county remains at the “high” CDC level of community transmission, but it could drop to “medium” in coming weeks.

Ferrer made the announcement during a briefing at which she displayed flat and declining data graphs. She said transmission has dropped steadily since July 23, “potentially signaling the beginning of a downward trend in cases.” Hospitalizations are also down.

“We're on a decline right now, and it’s hard for us to imagine reinstating universal indoor masking when we’re on this significant of a decline,” Ferrer said. But she added that health officials would reassess things should case rates and hospital admissions spike again.

While masks won't be required in most indoor spaces, Ferrer reminded residents that face coverings remain an effective tool to reduce spread.

As it has for most of the pandemic, LA County will still require masks in some indoor spaces, including health care facilities, Metro trains and buses, airports, jails and homeless shelters.

The new mandate, which would have gone into effect Friday, would have expanded the requirement to all indoor public spaces, including shared offices, manufacturing facilities, warehouses, retail stores, restaurants and bars, theaters and schools.

Nationwide, the latest COVID-19 surge is driven by the highly transmissible BA.5 variant, which now accounts for a majority of cases. It has shown a remarkable ability to get around the protection offered by vaccination.

It’s still unclear what enforcement of the health order might have looked like. Under past mandates, no individuals were cited for refusing masks, and officials favored educating people over issuing citations and fines.

Critics of a new mask rule said they didn't believe it would decrease or stop transmission rates. Los Angeles County Supervisor Kathryn Barger said she was pleased with Ferrer's announcement because “unenforceable mandates don't work.”

“I’m hopeful that we will now be able to move on from this heightened focus on masking mandates to what really matters — focusing on promoting the efficacy of vaccines and boosters, improving access to COVID-19 treatments, and continuing to educate our County’s residents on the benefits of masking,” Barger said in a statement Thursday. "I am comfortable leaving this decision in the public’s very capable hands.”

The LA County cities of Long Beach and Pasadena have their own health departments that typically align with LA County’s rules. But not this time. Both cities said this week that they would not impose requirements for face coverings.
And the City Council of Beverly Hills voted unanimously Monday to not adopt a mask mandate imposed by the county.
 

Heliobas Disciple

TB Fanatic
(fair use applies)

CanSinoBIO's inhaled COVID booster stronger against BA.1 Omicron subvariant than Sinovac shot
by Roxanne Liu and Ryan Woo
Fri, July 29, 2022, 2:05 AM

BEIJING (Reuters) - Chinese vaccine firm CanSino Biologic's inhalation-based candidate elicited a better antibody response as a booster against the BA.1 Omicron sub-variant than Sinovac's shot, but the antibody level dropped in months, clinical trial data showed.

The result came as top political leaders in China called for proper tracking of virus mutation and developing of new vaccines and treatments in the country's effort to refine its COVID control strategy.

China has given about 56% of its 1.41 billion population a booster dose using domestic shots, and most people were boosted with the same product as their primary series, despite growing evidence that some mix-and-max strategies would likely achieve higher antibody levels.

Among over 100 adults who received a lower dose of CanSinoBIO's inhaled vaccine candidate following two Sinovac shots, after four weeks, 92.5% developed the neutralising antibody that neutralises Omicron at levels that researchers defined as detectable, according to a paper published without peer review.

That compared with 88.9% for a higher-dose group, also with over 100 participants, said in a paper published late on Thursday.

The rate for both groups declined to around 70% after six months of the inhaled booster.

Barely any of the over 100 participants who received a third Sinovac shot had detectable neutralising antibody for Omicron after four weeks or six months.

The study did not compare CanSinoBIO's inhaled booster with other potential boosters that have triggered stronger antibody responses than a third dose of the Sinopharm or Sinovac shot.

Antibody-based readings reflect an important part of the vaccine-triggered immune response, and are different from the vaccine efficacy that indicates how well a shot reduces the risk of COVID disease, hospitalization or death.

The impact of BA.4 and BA.5 Omicron sub-variants on CanSinoBIO's inhaled vaccine deserves further study, said the authors, who worked at CanSinoBIO and other Chinese institutes.

CanSinoBIO's experimental inhaled vaccine uses a technology similar to that of its injection-based shot, which has been approved in countries including China, Mexico and Argentina, and AstraZeneca's vaccine.

The company is also testing a candidate based on the mRNA method in a mid-stage clinical trial in China.
 

Heliobas Disciple

TB Fanatic
(fair use applies)

Why Some Experts Suggest Getting a PCR Test, Even If You Already Know You Have COVID-19
Jamie Ducharme - TIME
Thu, July 28, 2022, 10:35 AM

For Rachel Robles, getting diagnosed with Long COVID was an uphill battle. She caught the virus in March 2020, when nearly nothing was known about its long-term effects and testing was inaccessible for most people.

To this day, she is sensitive to looking at screens—doing so can prompt pressure in her head and ringing in her ears—and has to manage COVID-19-related injuries to her liver and brain. But since she never got tested for COVID-19 when she first got sick, Robles had to “fight tooth and nail for every diagnosis I’ve received,” convincing doubtful doctors that she’d caught the virus and developed Long COVID.

She was eventually diagnosed with Long COVID, but it likely would have been easier if she had had the proof of infection that a test result provides, she says. Robles now recommends that anyone who suspects they have COVID-19 get a laboratory test, just in case they go on to develop Long COVID and need documentation of a previous infection for diagnosis or care.

“I never got proof of my initial COVID infection, and I was gaslit so much,” says Robles, who is an administrator at the Long COVID support group Body Politic and a contributor to the Patient-Led Research Collaborative for Long COVID. “So I always tell people, ‘This is something you need to do if you have a COVID infection, just in case.’”

David Putrino, a Long COVID researcher at New York’s Mount Sinai health system who co-authored a chapter of the forthcoming Long COVID Survival Guide with Robles and neurologist Dr. Dona Kim Murphey, says he “wholeheartedly” agrees that people should get as much documentation of an infection as possible. Getting a PCR test is “100% the recommendation”—but if all you can do is take an at-home test, at least keep photos of the results, Putrino says.

“Covering your bases as soon as you start to feel unwell and keeping good records is super important,” he says. (In the book chapter, Putrino, Murphey, and Robles even recommend that people consider getting blood tests and chest X-rays done soon after they get diagnosed with COVID-19, so they have a baseline record in case they later experience complications.)

PCR tests are still considered the gold standard for accuracy, so some doctors recommend getting one to confirm the results of an at-home swab. But people are increasingly forgoing that step now that rapid tests are widespread and increasingly accepted. A PCR test isn’t even required to get a prescription for the antiviral Paxlovid.

It may seem paranoid to plan ahead for a possible case of Long COVID—but the odds of getting it aren’t so long. Recent federal data suggest that one in five people who catches COVID-19 will develop symptoms of Long COVID, which can include fatigue, cognitive dysfunction, and chronic pain, among many others.

If someone does develop Long COVID, having documentation of a previous COVID-19 case could make it easier to get properly diagnosed or treated in a Long COVID clinic, some of which require either proof of previous infection or a positive antibody test. But not all patients have such proof.

In July, Hannah Davis—who is also part of Body Politic and the Patient-Led Research Collaborative for Long COVID—said in Congressional testimony that PCR and antibody tests “are often required for sick leave, entry into Long COVID clinics, health care, and participation in research,” even though some people get false negative results and others can’t get tested at all. Davis added that some people who catch COVID-19 do not produce antibodies, or see their antibody levels drop to undetectable levels over time.

Dr. Hector Bonilla, who co-directs Stanford’s Post COVID-19 Syndrome Clinic, says his facility accepts a patient as long as they have a positive test result linked to their name—that is, one done by a clinician or testing service, as opposed to a do-it-yourself home test—or evidence of infection-related antibodies. Having a COVID-19 test result can help determine whether someone has Long COVID or other, similar illnesses, such as myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Bonilla says. (Some Long COVID patients also meet diagnostic criteria for ME/CFS.)

But Dr. Benjamin Abramoff, who directs Penn Medicine’s Post-COVID Assessment and Recovery Clinic, says he thinks fewer clinics will require official test results now that at-home tests are the norm. “Realistically, everybody’s going to be getting home tests,” he says. “I can’t imagine anyone requiring [formal testing] moving forward.”

And while many Long COVID patients without PCR test results were outright dismissed by doctors early in the pandemic, Abramoff thinks that’s happening less now that Long COVID is more widely known. “It still happens, but much less than it did,” he says. Even without a PCR test result, documentation from a doctor can be enough to get disability benefits, insurance coverage, and work accommodations, he says. Many long-haulers struggle to get disability benefits even with proper documentation, however.

Maria Van Kerkhove, the World Health Organization’s (WHO) technical lead for COVID-19, said in a statement to TIME that “the lack of proof of prior infection shouldn’t be an impediment for people to get access to diagnosis and care” for Long COVID. The WHO’s definition of Long COVID specifies that it can occur among people who have either a “probable or confirmed SARS-CoV-2 infection,” she noted.

Still, Putrino says it’s better to be safe than sorry, as the criteria for getting a Long COVID diagnosis or being admitted to a treatment center vary by institution and could change in the future. “Those diagnostic criteria can change based on who’s in power,” he says. “Making sure that you have very clear documentation of a positive test is important, because it gives you your best chance of being able to receive services as long as you need them.”
 

Heliobas Disciple

TB Fanatic
(fair use applies)

Even mild COVID cases can result in symptoms that persist for 2 years, NJ study finds
Scott Fallon, NorthJersey.com
Thu, July 28, 2022, 5:26 PM

Patients who never needed hospitalization for COVID-19 early in the pandemic were still experiencing at least one persistent symptom a year later, showing that even mild cases can result in long-term health problems, researchers at St. Joseph's Health in Paterson announced Thursday.

In a study that for two years tracked 173 St. Joseph's patients with mild and severe COVID cases, about half — including some who had mild cases — still had shortness of breath, fatigue, body aches or other ailments a year after infection. About 23% of patients were experiencing at least one symptom two years later.

“Our study is the first to show that even patients with only mild COVID-19 infections can still have persistent symptoms after two years,” said Dr. Christopher Millet, one of the researchers.

Although research is ongoing across the globe on long COVID, there is much that scientists and physicians don't know about lingering symptoms in adults and children. Complicating the research is that the original strain has continually mutated into new variants, from delta that hit New Jersey hard late last summer to several omicron subvariants currently circulating the globe and causing cases to spike.

Long COVID has been found most often in those who initially experienced severe illness, but has also been found in more mild cases, according to the Centers for Disease Control.

There is no test to diagnose long COVID, and health officials caution that patients may have similar symptoms that could come from other health problems. The St. Joseph's study acknowledged it had limitations with a small patient size, the accuracy of patients' memory and the loss of some patients for follow-up questions.

Still, the patients in the study were among the first infected with COVID during the pandemic, in March and April of 2020 when St. Joseph's was one of the hardest hit hospitals catering to densely populated lower Passaic County communities. No vaccines were available during that period and therapeutics had not yet been fine-tuned.

Millet, who had been infected in March 2020 while working at St. Joseph's, experienced symptoms for months. "I had looked for research on this at the time and there was virtually none," he said. "That was the starting point. We had been hit so early that we knew we had a lot of patients that we could go to and collect information on over the years."
Of the 173 patients recruited, 91 had been hospitalized.

The study also focused on minorities, which make up a sizable portion of the communities St. Joseph's serves. About 47% of patients in the study were Hispanic and 28% African American.

Persistent COVID symptoms one year later

At the one-year mark, the most common recurring symptoms among all patients were:
  • 25% shortness of breath
  • 24% fatigue
  • 21% anxiety
  • 18% difficulty focusing
  • 18% body aches
  • 16% headaches
About 50% of those reporting symptoms at the one-year mark were not hospitalized, Millet said in an interview.

While symptoms stopped in most patients by the two-year mark, shortness of breath and fatigue were still the most common ailments. The majority of those still having symptoms in year two were hospitalized. Women were more likely to have persistent symptoms at two years compared to men, the study showed.

Millet hopes the study will be a building block for further research into long COVID.

"There's still so much we don't know about it more than two years into this pandemic," he said. "But we've shown that symptoms can last as long as two years even in patients who had mild symptoms. That alone advances the science. The next question is how are these patients going to cope with symptoms that may be lifelong?"
 

Heliobas Disciple

TB Fanatic
(fair use applies)

Japan looks to regions to mount COVID fight as variant spreads
Mariko Katsumura and Elaine Lies
Thu, July 28, 2022, 8:28 PM

TOKYO (Reuters) -Japan is encouraging regional authorities to take their own counter-measures against the spread of a new coronavirus variant that has sent cases surging to record levels, but there is no plan for any sweeping national measures.

A seventh wave of COVID-19 pushed the daily tally of new cases in Japan to a record 233,094 on Thursday as the BA.5 variant of virus spreads, putting pressure on medical services and disrupting company operations in some places.

Japan has never imposed national lockdowns on the scale of some other countries, instead periodically calling on people to stay at home as much as possible and limiting the opening hours of restaurants and bars.

Deputy Chief Cabinet Secretary Seiji Kihara reiterated that on Friday saying regional authorities should tailor their response to their specific situations.

"Rather than a national response, we want to support regional authorities in their efforts that are based on their local situations," Kihara told a regular news conference.

"What's important is to help each prefecture's social and economic activities."

The western city of Osaka recently urged elderly people to avoid non-essential outings.

Tokyo governor Yuriko Koike called on residents to test frequently, including at free centres set up at city train stations, and to maintain precautions such as masks but the capital was not imposing any restrictions at this point.

"We've learned a lot from our experiences over the past few years," she told a regular news conference.

The country of 125.8 million people has done better than some in handling the pandemic, with 32,308 deaths since it began in early 2020.

But Japan had the world's highest number of new coronavirus cases in the week to July 24, the World Health Organization said this week.

Though the number of deaths in the new wave has been low compared with previous ones, new infections are beginning to take a toll on some sectors.

Train companies in some regions have had to curtail services due to a lack of staff and Toyota Motor Corp suspended night shift operations at one production line of its Takaoka factory in central Japan this week because of COVID..
 

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After Biden COVID recovery, admin launches new booster push
ZEKE MILLER
Thu, July 28, 2022, 3:44 PM

WASHINGTON (AP) — President Joe Biden's administration is launching a renewed push for COVID-19 booster shots for those eligible, pointing to the enhanced protections they offer against severe illness as the highly transmissible BA.5 variant spreads across the country.

The initiatives include direct outreach to high-risk groups, especially seniors, encouraging them to get “up to date” on their vaccinations, with phone calls, emails and new public service announcements.

All Americans age 5 and over should get a booster five months after their initial primary series, according to the Centers for Disease Control and Prevention. It also says those age 50 and over — or those who are immunocompromised — should get a second booster four months after their first. According to CDC, tens of millions of eligible Americans haven’t received their first booster, and of those over 50 who got their first booster, only about 30% have received their second.
CDC has released a "booster calculator” to help people determine when to get a booster shot.

Biden, who received his second booster shot in March, tested positive for the virus last week and recovered after experiencing mild symptoms for five days.

“Given the rise of the Omicron BA.5 variant, it is essential that Americans stay up to date on their COVID-19 vaccinations — with booster shots — to achieve the highest level of protection possible,” the White House said. COVID-19 is killing about 366 people in the U.S. each day, the vast majority of whom are not up-to-date on their vaccinations. The administration says those deaths are largely preventable.

In May, according to the CDC, prior to the dominance of the BA.5 variant in the U.S., people over 50 with only a single booster shot were four times more likely to die of COVID-19 than those with two or more booster doses.

“Currently, many Americans are under-vaccinated, meaning they are not up to date on their COVID-19 vaccines,” CDC Director Dr. Rochelle Walensky said earlier this month. “Staying up to date on your COVID-19 vaccines provides the best protection against severe outcomes.”

As part of the new booster push, the White House says pharmacies in the federal pharmacy program will step up outreach to those eligible for another booster dose. It says Walgreens will make more than 600,000 phone calls, and Rite Aid will send nearly 9 million emails to people encouraging them to get shots.

The Centers for Medicare & Medicaid Services will also reach out to 600 nursing homes that have reported booster uptake rates under 80% to offer additional federal support, including on-site clinics and sending medical providers and infectious disease experts to educate people about the benefits of the shots. CMS will also email booster reminders to the 16 million people who receive their Medicare emails and added a booster reminder message to its 1-800-MEDICARE call-in line.

The U.S. Department of Health and Human Services will also continue to run PSAs encouraging boosters during commercial breaks on shows with significant viewership among seniors, like “NCIS Hawaii,” “Good Morning America,” “Jimmy Kimmel Live” and “48 Hours
 

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White House rewrites rules to push more affordable housing with COVID-19 rescue funds
Joey Garrison, USA TODAY
Thu, July 28, 2022, 12:37 PM

WASHINGTON – The Biden administration is expanding ways cities and states can use COVID-19 rescue funds to build more affordable housing amid skyrocketing home prices.

New guidance from the Treasury Department on Wednesday gives local and state governments greater flexibility to address affordable housing with their share of $350 billion in direct aid from the American Rescue Plan – President Joe Biden's signature COVID-19 stimulus law that Democrats in Congress passed in March 2021.

What the changes mean
  • State and local governments will be able to use American Rescue Plan funds to finance long-term affordable housing loans to nonprofits and developers. The loans must extend at least 20 years and offer affordably priced units for households earning 65% or less of the area's median income over that same duration. Previously, loans were subject to more restrictions.
  • New rules allow cities and states to direct COVID-19 rescue funds to six additional federal housing programs – opening up money for low-income housing credits, affordable housing preservation, supportive housing for the elderly and disabled, and public housing capital projects. Currently, funds are limited to just two programs: the National Housing Trust Fund and HOME Investment Partnerships Program.
  • The Biden administration is clarifying that American Rescue Plan funds can "finance the development, repair or operation" of any affordable rental housing unit. Although many cities and states have committed funds toward affordable housing, others have had questions about whether they can use the money this way.
Thee Biden administration announced updated guidance Wednesday that gives greater flexibility for local and state governments to address affordable housing with their share of $350 billion in direct aid from the American Rescue Plan. Here, Biden, who continues to recover from a COVID-19 infection, listens to aides Monday at a virtual event from the White House.

The bigger housing picture
  • The U.S. has a shortfall of 1.5 million homes, according to Moody's Analytics, an economics research firm based in New York. The crunch has helped further fuel a spike in rental and sale prices that has intensified during the pandemic.
  • Biden, who faces pressure to find solutions to 40-year high inflation, put forward a goal in May to close the "housing supply gap" in five years.
  • In a testament to the housing crisis, more than 600 cities and states have already collectively devoted $12.9 billon in direct aid from the American Rescue Plan to housing. That tops the money spent on public safety, which Biden has repeatedly encouraged cities and states to prioritize. The only more popular use of the funds has been replacing depleted tax revenue to shore up budgets.
What they are saying
  • Wally Adeyemo, deputy Treasury secretary, said affordable housing advocates and builders pushed for the changes. "Our goal here is to address the price pressures Americans are facing," he said, pointing to the administration's support of legislation to lower prescription drug prices as another step in that effort.
  • Democratic members of Congress also lobbied for the changes, sponsoring legislation called the LIFELINE Act to boost affordable housing with COVID-19 rescue funds. "This is a major win for increasing housing stock and lowering the cost of housing for thousands of Americans," said Rep. Alma Adams, D-N.C., one of the sponsors.
  • Stockton Williams, executive director of the National Council of state Housing Agencies, said the existing "quirky language" in the American Rescue Plan law has prevented cities and states from maximizing the funds for affordable housing. He said the new rules will allow COVID-19 rescue funds to work "in tandem" with other funds for housing.
  • Gene Sperling, the White House's American Rescue Plan coordinator and a senior adviser to Biden, said the new guidance would "unlock" significantly more financing for affordable housing. Most cities and states have already decided how they're spending their American Rescue Plan funds. Even so, Sperling said the greater flexibility will offer cities and states focused on affordable housing "a bigger bang for their buck."
 

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Has The Lab Leak Theory Really Been Disproved?
by Tyler Durden
Thursday, Jul 28, 2022 - 11:50 PM

Authored by Matt Ridley via The Spectator (emphasis ours),

The BBC carried a story this week with the headline ‘Covid origin studies say evidence points to Wuhan market’. Bizarrely the paper in Science they are referring to, by Michael Worobey and colleagues, says no such thing. It says: ‘the observation that the preponderance of early cases were linked to the Huanan market does not establish that the pandemic originated there’.

All three of the scientists quoted in the BBC story have been highly dismissive about even discussing the possibility that the pandemic began as an accident in a Wuhan laboratory. Their vested interest is clear: they worry that the reputation of their field of virology would be threatened by such a discussion. But the many scientists who say such a debate is needed are largely ignored by the BBC: none are quoted in this week’s article.

The Beeb’s story says that ‘this evidence paints a picture that Sars-CoV-2 was present in live mammals that were sold at Huanan market in late 2019’. This too is wrong. Nobody has found any evidence of Sars-CoV-2 in live mammals at the market. They have found some evidence – they cite only a YouTube video – that mammals were on sale in the market, which we already knew, but not that the mammals were infected. That would be the very minimum requirement for asserting that the pandemic began in the market. In 2003 scientists refused to assert that Sars began in markets till they found infected animals.

The new paper shows that lots of early cases had visited the Huanan seafood market or lived near it, which we already knew. But for the first two weeks of January 2020, the Chinese authorities were defining pneumonia cases as (what we now call) Covid only if they had visited or lived near the market: so it is a circular argument. The scientists dismiss this ‘ascertainment bias’ problem by citing one of their own papers, which simply asserted that this problem could be ignored. As Dr Alina Chan of MIT and Harvard puts it: ‘Worobey et al. are claiming that there is no ascertainment bias because their lead author said so.’

The new Science paper has an ignominious history. It began life as a ‘preprint’ whose data and logic were torn apart within days by independent researchers. Even the Chinese Academy of Sciences panned it for ‘obfuscating the epidemic outbreak place…and the origin’ and for ‘overstating conclusions based on limited data and unrealistic simulations’. Senior Chinese scientists published a preprint the same week reiterating their conclusion that the market was a place where the early outbreak was amplified, not where it began. It’s quite something when western scientists go further than those supervised by the Chinese Communist party in trying to exonerate a possible lab leak. Yet its conclusions were reported by the Times as having ‘found patient zero’ and the New York Times as saying 'the virus was present in animals’ at the market – both entirely false claims.

As published, the paper is now a damp squib. Gone is all the certainty of the preprint. Where the preprint claimed ‘dispositive evidence for the emergence of Sars-CoV-2’, the paper now cites ‘insufficient evidence to define upstream events’. Where the preprint said the market was the ‘unambiguous epicentre’ of the pandemic, the published paper now admits that ‘exact circumstances remain obscure’.

There is one very misleading sentence: ‘This region of Hubei contains extensive cave complexes housing Rhinolophus bats, which carry SARS-CoVs’. The bat colonies near Wuhan have been extensively sampled, very few SARS-like viruses were found, and none at all like SARS-CoV-2. Most serious scientists agree that this virus probably came from bats on the borders of Yunnan and Laos. The question is and always has been: how did the virus get to Wuhan from bats living more than a thousand miles to the south-west, a distance as great as London to Rome?

One possibility is the wildlife trade, but far less wildlife is sold in Wuhan than in Guangdong in southern China, and yet the virus appeared only in Wuhan: where are the other outbreaks among wildlife traders. The other possibility is that it was scientists who brought it to Wuhan. Why do we think this still needs discussing? Here are six good reasons.

1. Wuhan is the site of the most intensive programme of research on SARS-like viruses in the world
2. That programme involved bringing hundreds of SARS-like viruses to Wuhan
3. Most of them were brought by scientists from Yunnan and some from Laos
4. Among those viruses was one that was 96.2 per cent the same as SARS-CoV-2
5. They refuse to open up their database showing what other viruses they brought and they published the results of experiments in which they manipulated the genomes of these viruses in ways that sometimes made them much more infectious
6. They published plans to insert into a SARS-like virus the very kind of genomic sequence that SARS-CoV-2 has and no other SARS-like virus has.

None of this is a smoking gun, but it’s a heck of a coincidence.
 

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Biden Admin To Unveil Reformulated Booster Shots In September
by Tyler Durden
Thursday, Jul 28, 2022 - 10:50 PM

The Biden administration is aiming for a mid-September rollout for reformulated Pfizer and Moderna COVID-19 booster shots, after both companies promised they would be able to deliver doses by then, according to the New York Times, citing people familiar with the deliberations.

The new versions are expected to perform better against then now-dominant (yet far more mild than Delta) BA.5 Omicron subvariant, though the Times notes that data on the reformulated shots is still preliminary.

As such, federal officials have decided not to expand eligibility for the next round of existing boosters this summer - which have only been approved for Americans over 50, or those over the age of 12 who have immune deficiencies.

Dr Fauci, interestingly enough, apparently didn't get his way, as the Times reports that he was pushing for more of the current vaccine to go into arms before the reformulated version is ready.

In internal deliberations, some senior health officials argued that eligibility for a second booster should be broadened before the reformulated version is ready because coronavirus infections are on the rise again. Dr. Anthony S. Fauci, the president’s chief medical adviser, and Dr. Ashish K. Jha, the White House pandemic response coordinator, both advocated that position. -NYT

"I think there should be flexibility and permissiveness in at least allowing" a second booster for younger Americans, Fauci told the Times earlier this month.

Another alternative under discussion was offering the shots only to a subset of younger, at-risk individuals - such as pregnant women (who don't have periods to disrupt!).

The FDA and the CDC, however, said the government should concentrate on a fall campaign for the reformulated doses, as long as they were ready for 'prime time' (disregarding the typical decade of so development and safety testing for most vaccinations, of course). Both Pfizer and Moderna said millions of doses would be ready by mid-September, so regulators made the call to wait for those shots.

All adults are expected to be eligible for the updated boosters, while Children could be eligible as well according to insiders.

According to the Biden administration, anyone who is eligible for shots now should just get them as opposed to waiting for the fall - despite its reduced efficacy against Omicron vs. the original strains it was developed for.

The Times notes that "Deaths from Covid-19 are still heavily concentrated among older age groups, while hospitalizations remain well below the peak of the Omicron wave last winter."

One concern was assuring that people did not get a booster now followed by another with the updated formulation too soon after. Officials worried that, especially for young men, two boosters in close succession might elevate the risk of a rare heart-related side effect, myocarditis, that has been linked to both Pfizer’s and Moderna’s vaccines.
For other reasons, immunologists warn against receiving booster shots in short intervals. -NYT

"You can’t get a vaccine shot Aug. 1 and get another vaccine shot Sept. 15 and expect the second shot to do anything," said La Jolla Institute of Immunology virologist, Shane Crotty. "You’ve got so much antibody around, if you get another dose, it won’t do anything."

"The antibodies stop that next dose from working" if the next dose is administered too early, he continued.

It will be interesting to see how many people actually get booster shots, given that federal officials are already concerned over the 'public's patience with additional shots,' according to the Times, which notes that the number of people getting the jab has been dropping more with each new one offered - to the point where fewer than 30% of eligible Americans have elected to receive a second booster, which would be their fourth total shot.

To accomplish the rollout, the Department of Health and Human Services made an advance purchase of 105 million doses of Pfizer's reformulated offering for $3.2 billion, with a possible fall deployment in mind. A similar agreement with Moderna is expected soon.
 

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Rand Paul Demands Answers After NIH Admits Redacting COVID-19 Origins Emails 'To Prevent Misinformation'
by Tyler Durden
Thursday, Jul 28, 2022 - 07:30 PM

Senator Rand Paul (R-KY) is demanding answers from the National Institutes of Health (NIH), after he says the agency "has repeatedly disregarded its responsibilities under FOIA (Freedom of Information Act) and the American people's right to agency records," according to a Wednesday letter from Paul to NIH Acting Director Lawrence A. Tabak.

"For almost two years, public interest groups and media organizations have been forced to engage in protracted litigation to obtain documents related to NIH's involvement in COVID-19," adding "The records NIH has produced have been heavily redacted."

"This suggests NIH is censoring the information it releases to the public about the origins of the pandemic."

Paul cites an article by journalist and former Chuck Grassley investigator Paul D. Thacker, which notes an egregious admission by the NIH in Court that the agency "is withholding portions of emails between employees because they "could be used out of context and serve to amplify the already prevalent misinformation regarding the origins of the coronavirus pandemic.""

Senator @RandPaul cites @DisInfoChron and asks if @NIH to explain if it is "censoring information it releases to the public about the origins of the pandemic." https://t.co/jkj0IhZhDV
— Paul D. Thacker (@thackerpd) July 27, 2022

In an 18-page declaration to the court, NIH FOIA Officer Gorka Garcia-Malene detailed how the NIH redacts documents in compliance with the law. In the case of Exempt 6 privacy concerns, Garcia-Malene declared:
Exemption 6 mandates the withholding of information that if disclosed “would constitute a clearly unwarranted invasion of personal privacy.” 5 U.S.C. § 552(b)(6). Exemption 6 was applied here due to the heightened public scrutiny with anything remotely related to COVID-19.
Mr. Garcia-Malene also claimed that information had be redacted “because of the amount of misinformation surrounding the pandemic and its origins.” Seriously, the NIH is now arguing in court that because there is so much misinformation about how the pandemic began, they can’t release facts that might clear up misinformation about how the pandemic began.

The NIH was responding to a case brought by US nonprofit Right to Know, after the NIH deleted coronavirus sequences that Chinese researchers added to the NIH's Sequence Read Archive. As Thacker notes, "These datasets involved key studies that virologists were using at the time to promote the now discredited theory that the COVID-19 virus may have passed from pangolins to humans."

In the case at hand, the NIH attempted (and succeeded) at sealing the name of a Chinese researcher which had already been made public.

More via Disinformation Chronicle:

Last week, the NIH filed a motion in a Virginia court to seal portions of documents that reference the Chinese researcher and an NIH official in a lawsuit filed against the agency for redacting and covering up records that might explain how the pandemic began.

“[T]he individuals have a substantial privacy interest in avoiding harassment or media scrutiny that would likely follow disclosure,” wrote a lawyer for the NIH to the judge. “Sealing is therefore necessary to protect this information from any further public dissemination.”

But what is actually being protected? The American public’s right to access public information that may reveal what kicked off the pandemic, or the purported privacy rights of a scientist who lives thousands of miles away in China? This legal ploy further highlights the NIH’s aggressive, haphazard approach to redacting documents and hiding information that might explain how the pandemic started.

Last summer Buzzfeed released an investigation of the NIH’s Anthony Fauci and reported that the documents the agency released were "just a portion of what was requested, and they are filled with redactions, making them an incomplete record of the time period and Fauci's correspondence." Meanwhile, the Intercept reported in February that the NIH continues to withhold critical documents that could shed light on how the epidemic began, noting that the agency sent them 292 pages of fully redacted records.

Among these pages, the NIH fully redacted the 2020 COVID-19 research plan put together by Anthony Fauci.
A week after The Intercept story, The Chief Records Officer for the U.S. Government sent the NIH a letter asking them to investigate allegations that agency personnel are shredding documents related to grant-making decisions and funding for research in China.

Kangpeng Xiao’s name became public in December 2020, when the nonprofit U.S. Right to Know published a report on revisions to coronavirus sequences that Chinese researchers had added to the NIH’s Sequence Read Archive. These datasets involved key studies that virologists were using at the time to promote the now discredited theory that the COVID-19 virus may have passed from pangolins to humans.

“These revisions are odd because they occurred after publication, and without any rationale, explanation or validation,” wrote Sainath Suryanarayanan, in the December 2020 report for U.S. Right to Know. The nonprofit based their report on NIH documents they received from a FOIA request.

According to these documents, several Chinese scientists asked the NIH to alter coronavirus sequences stored on the NIH database, with many of these requests coming from Kangpeng Xiao with the South China Agricultural University. In one case, Xiao asked NIH official Rick Lapoint in March 2020 to delete some coronavirus sequences.



A few months later, Xiao published a prominent paper on May 7, 2020, in the journal Nature that argued a coronavirus discovered in pangolins was closely related to COVID-19. But as U.S. Right to Know discovered, Xiao’s request to delete coronavirus sequences from the NIH’s Sequence Read Archive (SRA) was just one of many changes.

Xiao et al. made numerous changes to their SRA data, including the deletion of two datasets on March 10, the
addition of a new dataset on June 19, a November 8 replacement of data first released on October 30, and a further data change on November 13 — two days after Nature added an Editor’s “note of concern” about the study.

Eventually, Nature’s “note of concern” attached to Xiao’s 2020 study changed to a very lengthy correction in late 2021 that explained that data “were mislabelled and attributed incorrectly.” That correction also thanked Alina Chan of Harvard and the Broad Institute “for bringing the errors to our attention.” Chan later tweeted that Nature refused to publish her analysis of the viruses and merely folded her study into their correction.

The next time a mysterious outbreak occurs, will we see a repeat performance of inaccurately written papers published in top journals and the dismissal of independent analyses demonstrating that these studies are not reproducible/accurate based on the available data?
— Alina Chan (@Ayjchan) November 12, 2021

NIH coronavirus database becomes national news

This U.S. Right to Know report was largely ignored, but last summer, coronavirus sequences at the NIH SRA became national news when Jesse Bloom, a virologist at the Fred Hutchinson Cancer Center, published a preprint on NIH sequences that Chinese researchers had deleted. As Bloom explained in an email to NIH leadership at the time, “[T]his can be a good opportunity for the NIH to take the lead by using its remarkable data archives to make progress in resolving some of the important questions about the virus’s origins.”

The NIH would not disclose to reporters the names of Chinese researchers who requested sequence deletions, but the New York Times later identified one of the scientists as Ben Hu at Wuhan University.

Empower Oversight referenced Kangpeng Xiao’s identity in federal court recently on July 11, when the nonprofit charged that the NIH was improperly redacting documents when responding to their FOIA requests. In one case, the NIH had provided Empower Oversight with an October 12, 2021, email from Jesse Bloom to the NIH discussing a scientist’s request to delete NIH SRA sequences. Citing Exemption 6, which covers privacy concerns, the NIH redacted both the names of the requestor and the NIH official that Bloom cited in his email

Read the rest from Thacker here...


Paul has demanded the NIH answer the following questions:
 

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Judge Orders Air Force Not to Punish Members Seeking Religious Exemptions to COVID-19 Vaccine Mandate
By Zachary Stieber
July 28, 2022

Air Force officials were ordered on July 27 not to discipline airmen who are seeking religious exemptions to the military’s COVID-19 vaccine mandate.

U.S. District Judge Matthew McFarland, a Trump appointee, entered a preliminary injunction against the military branch.
McFarland two weeks earlier issued a temporary restraining order. He asked the military to make its case as to why he shouldn’t enter a preliminary injunction, a longer-lasting measure.

In a 16-page filing, government lawyers said blocking the military from punishing unvaccinated members “would interfere with ongoing legal proceedings and would otherwise be improper, particularly in light of significant new developments.”

Among the developments, they pointed to U.S. drug regulators authorizing a COVID-19 vaccine made by Novavax. Unlike the three shots previously available in the United States, the Novavax vaccine doesn’t use fetal cells in its development, manufacturing, or production.

“Those class members whose religious objections were based on mRNA technology or the use of fetal-derived cell lines are no longer substantially burdened by the COVID-19 vaccine requirement because this option is now available,” the lawyers said.

Included in the opposition was a declaration from Lt. Gen. Kevin Schneider, the director of staff for the Air Force’s headquarters. He claimed that unvaccinated members “are at a higher risk of contracting COVID-19 and substantially more likely to develop severe symptoms resulting in hospitalization or death” and that exempting a large number of airmen “would pose a significant and unprecedented risk to military readiness and our ability to defend the nation.”
Of the 14 members who died with COVID-19 since March 14, according to Schneider, 12 were unvaccinated.
McFarland wasn’t convinced.

“Defendants fail to raise any persuasive arguments,” he said.

Chris West, an attorney representing the plaintiffs, called the ruling “such a big win” on Twitter.

Thousands Affected

The Air Force has approximately 497,000 members. Of those, 97.1 percent have received a primary series of a COVID-19 vaccine as of July 11.

About 1,440 exemptions to the mandate have been granted, including 104 religious exemptions. Another 2,847 are pending, and 6,803 have been rejected.

The small number of religious exemptions granted is “farcical,” McFarland said earlier this year. He said that the Air Force “‘has effectively stacked the deck’ against service members seeking religious exemptions.”

Under the new order, the Air Force can’t take disciplinary action against, or attempt to kick out, members who have requested a religious exemption on or after Sept. 1, 2021, and were deemed by a chaplain as having a “sincerely held religious belief.” Most military members who apply do and were either denied or haven’t had action on their request.
 

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BioNTech, Pfizer Sue CureVac in US Over COVID-19 Vaccine Patent Claims
By Ludwig Burger - Reuters
July 28, 2022

FRANKFURT—COVID-19 vaccine maker BioNTech said on Tuesday that it and partner Pfizer have filed a complaint with the U.S. District Court in Massachusetts, seeking a judgment that they did not infringe U.S. patents held by rival CureVac.

The lawsuit, filed Monday, said CureVac is trying to profit from the success of BioNTech and Pfizer’s COVID-19 vaccines after CureVac’s efforts to create its own vaccine failed.

CureVac earlier this month filed a patent lawsuit in Germany against BioNTech over its use of mRNA technology and did not rule out further legal action against BioNTech’s partner Pfizer or rival mRNA vaccine maker Moderna Inc..

BioNTech said that CureVac’s U.S. patents were equivalent to German patents invoked by CureVac in the German court case.

BioNTech and Pfizer asked the Boston court to declare that their Comirnaty vaccine does not violate three CureVac patents related to RNA-based vaccines. The companies told the court that Comirnaty does not work in the same way as CureVac’s patented technology.

One of the patents concerns messenger RNA (mRNA) connected to lipid nanoparticles (LNPs), which the vaccines use to deliver the molecules safely into the body. Pfizer, BioNTech, and Moderna have been hit with U.S. patent lawsuits by other biotech companies this year over the LNP technology used in their vaccines.

Pfizer has said that it expects $32 billion in revenue from Comirnaty this year.

CureVac said in a statement it was aware of BioNTech’s legal action but had not yet been formally served.

“We will review the matter legally in detail and represent our position accordingly,” it added.
 

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Judge Sides With NIH, Agrees to Redact Name of Chinese Researcher
By Zachary Stieber
July 27, 2022

A U.S. judge has sided with the National Institutes of Health (NIH) and ordered the sealing of a Chinese scientist’s name, even though the name was made public by the NIH in 2020.

U.S. Magistrate Judge John Anderson on July 22 ordered documents listing the name placed under seal, granting a motion by the NIH.

The documents had been released by the NIH to Empower Oversight, the plaintiff in the case.

Anderson said he found that the “targeted and limited sealing” was “the least drastic alternative available” and that First Amendment presumptions in favor of public access to records were outweighed for reasons set forth in the NIH’s filings.
The NIH had said that it “inadvertently failed” to redact the names of the Chinese scientist and the NIH worker who corresponded with the scientist.

While the Freedom of Information Act requires agencies to disclose such information, the names were redacted elsewhere in filings under an exemption that covers the release of information that would be a “clearly unwarranted invasion of privacy,” government lawyers conveying the NIH’s position told the court.

“Exemption 6 was applied here due to the heightened public scrutiny with anything remotely related to COVID-19. Consequently, all email addresses, direct telephone numbers, identities of the submitter and NIH database curators that the submitter dealt with, have been withheld,” Gorka Garcia-Malene, an NIH official, said in a declaration to the court, adding that “there is no public interest in the disclosure of this information.”

Order Entered Too Soon

Empower Oversight responded in a motion on July 27, asserting that the judge entered his order too soon.

“The order was issued before Empower Oversight timely filed its opposition to NIH’s motion to seal,” plaintiffs said in the filing.

The nonprofit noted that it had seven days to respond to the NIH’s July 15 motion, but that Anderson entered the order before that period of time elapsed.

Opposition to the motion was filed on July 22. But Anderson did not consider the opposition because his order was entered five minutes earlier, according to the court docket.

Anderson’s chambers referred a request for comment to the clerk’s office for the U.S. courthouse in Alexandria, Virginia. The clerk’s office said it would only respond to inquiries sent by mail.

Empower Oversight asked the judge to set aside the order and ultimately reject the government’s motion.

No ‘Compelling Government Interest’

The Chinese scientist in question was identified as Kangpeng Xiao of South China Agricultural University in an exhibit that is now under seal. Xiao successfully lobbied the NIH to remove data his team submitted to the Sequence Read Archive, a database the agency manages.

The team had submitted sequencing data from a pangolin-derived coronavirus that researchers claimed was very similar to SARS-CoV-2. Also known as the CCP (Chinese Communist Party) virus, SARS-CoV-2 causes COVID-19. The team’s research, which was later corrected, was published in Nature.

Xiao’s name has been public since 2020, when another nonprofit, U.S. Right to Know, published emails (pdf) showing his correspondence with the NIH. The messages were highlighted by Jesse Bloom, a Fred Hutchinson Cancer Research Center researcher, in a preprint paper (pdf) he authored on the deleted data.

The emails and paper were released months before the NIH provided Xiao’s name to Empower Oversight.

“Thus, the information that NIH now seeks to seal was already public before it produced the relevant email to Empower Oversight,” the nonprofit said in an opposition filing. Plaintiffs also said the Freedom of Information Act doesn’t provide any “‘heightened’ protections” because of COVID-19 or any other matter.

The group argued that the NIH had failed to present “a compelling governmental interest” that supported sealing the name of Xiao and the NIH worker with whom Xiao corresponded.

Xiao could not be reached. His university did not respond to a request for comment.

Under Scrutiny

The NIH has been under scrutiny for its handling of requests from Xiao and other scientists, including one whose identity has not yet been confirmed.

That scientist asked in June 2020 for SARS-CoV-2 sequences to be pulled from the database, and the NIH complied.
The NIH has maintained that the data was still accessible, but only offline.

That was an “error” Dr. Lawrence Tabak, the agency’s acting head, told lawmakers in May.

He said the data should have instead been “suppressed,” which would have kept it online but made it harder to find than normal sequences.
 

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The Psychology of Totalitarianism
By Chris Martenson
Thursday, July 28th, 2022

Just over seven months ago, I helped introduce the world to Mattias Desmet and the concept of “Mass Formation” (aka Mass Psychosis). Nearly half a million people watched our video on our many social media channels and at the Peak Prosperity website.

Prominent voices like Dr. Robert Malone, Joe Rogan and many others quoted the show and Mattias, and the idea of a mass psychosis taking over our world became common knowledge.

I found profound relief at finally having a framework for understanding – and even having compassion for – my fellow citizens who seemed to be going, well, crazy. A light on a very dark path began to shine.

People who once relished freedom and Democracy, often sporting a healthy and well-earned distrust of government and pharmaceutical companies, suddenly became acolytes of those entities. They attacked anyone that questioned the obviously authoritarian actions of those same entities.

How could so many people turn into slaves of the very entities that they had shunned throughout their lives? They literally became the victims and the tools of totalitarian leaders…voluntarily?

Just so, how could so many so-called “trusted leaders” turn us – their constituents or customers or friends and family – down this horrid path? As I wrote for the original interview, these “dim actors” pull our emotional strings “to create fear and isolation in order to push their agenda of technocratic control of our lives, dreams of transhumanism, using vaccine passports as a first step on a path to overt totalitarianism.”

Early on, you might have justly given those bad actors a break; after all, it was a pandemic of a new virus. But it didn’t take long to see the truth behind actual science and data; yet these elites doubled down on their control.

In his newest book, “The Psychology of Totalitarianism” Mattias helps us understand how those we supposedly trusted are still trying to create a world in which they have full control.

As he writes, “Totalitarianism is not a coincidence and does not form in a vacuum. It arises from a collective psychosis that has followed a predictable script throughout history, its formation gaining strength and speed with each generation—from the Jacobins to the Nazis and Stalinists—as technology advances. Governments, mass media, and other mechanized forces use fear, loneliness, and isolation to demoralize populations and exert control, persuading large groups of people to act against their own interests, always with destructive results.”

While we may think the lies of the pandemic and authoritarians are being exposed, and there is a light at the end of the dark tunnel, the truth is that we’re still very much in danger. Climate change, Monkeypox, Ukraine, China, recession, supply chains…the list of emergencies are never-ending, and thus the excuses for more control are never-ending.

Take this to heart, the risks are as grave as ever. We few brave and courageous people must continue to stand up and say “No!” If we do not, Mattias shows exactly how throughout history good people ended up somewhere they deeply regretted. That could be us, soon.

The good news is that many more people are now waking up to the truth that government restrictions and mandates, seemingly endless fear-based public relations campaigns, lockdowns, forced medical procedures, and vaccine passports to travel in one’s own community were created not on the basis of sound science or firm data, but out of a desire to control.

Human misery and mass atrocities are always possible, but now more than ever, our “leaders” are pushing us in that direction. It is our solemn duty to resist.

As always, “It doesn’t have to be this way.” We can do better. Listen to this important interview so “they” can’t transfer their anger and rage at us.

Mattias tells us how it’s done, and what we can do. Of course, we must defend ourselves but never resort to unnecessary violence. Continue to be courageous. Hold everyone with compassion. Hate the sin, not the sinner. But most of all, we must speak up.

59 min 51 sec

~~~~~~~~~~

First 41 minutes can be seen here:
View: https://www.youtube.com/watch?v=L6hFHr6-uJo
Mattias Desmet: It's Time to Take a Stand
40 min 49 sec

Premiered 7 hours ago
 

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View: https://www.youtube.com/watch?v=BevSJKFkY8E
Could the COVID-19 vaccine have blunted immunity to Omicron infection?
14 min 19 sec

Streamed live 12 hours ago
Vejon Health

Insights from a recent paper looking at the immune response to Omicron infection for health care workers.

Read paper here:

Reynolds, Catherine J., et al. "Immune boosting by B. 1.1. 529 (Omicron) depends on previous SARS-CoV-2 exposure." Science 377.6603 (2022): eabq1841.

...
 

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View: https://www.youtube.com/watch?v=J1UzetqiWG4
Spike Protein Destroy Mitochondria (Studies)
51 min 40 sec

Streamed live 5 hours ago
Drbeen Medical Lectures

Do you wonder just how does the spike protein cause cell damage? In this study researchers provide a unique insight into the mechanism of damage and the evidence of damage in brain microglial cells using Ramen microspectrometer. Let's review.

URL list from Thursday, Jul. 28 2022

Mitochondrial Dysfunction: A Prelude to Neuropathogenesis of SARS-CoV-2 - PMC
https://www.ncbi.nlm.nih.gov/pmc/arti...

Mitochondrial Dynamics in SARS-COV2 Spike Protein Treated Human Microglia: Implications for Neuro-COVID - PMC
https://www.ncbi.nlm.nih.gov/pmc/arti...

SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE 2 | Circulation Research
https://www.ahajournals.org/doi/10.11...

SARS-CoV-2 membrane protein causes the mitochondrial apoptosis and pulmonary edema via targeting BOK | Cell Death & Differentiation
https://www.nature.com/articles/s4141...

SARS-CoV-2 membrane protein causes the mitochondrial apoptosis and pulmonary edema via targeting BOK
https://www.nature.com/articles/s4141...

Raman Microspectrometer | Raman Spectra | Supplier
https://www.microspectra.com/support/....
 

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COVID-19: New energy for flagging immune cells
by University of Bonn
July 28, 2022

In severe COVID-19 patients, metabolism produces insufficient amounts of certain energy-rich compounds called ketone bodies. However, these energy carriers are needed by two important cell types in the immune system in order to fight the virus effectively. This finding could explain why some people fall ill so much more severely than others. A study led by the University of Bonn (Germany) at least points in this direction. The results have now been published in the journal Nature. They also give hope for new therapies.

Appetite often declines during illness. This also has an effect on metabolism: Since it is no longer as well supplied with carbohydrates, it switches to burning fat. This creates energy-rich molecules called ketone bodies, which may help the body to cope better with viruses.

At least that is what the results of the current study suggest. "We found that patients with influenza infections produce ketone bodies in considerable quantities," explains Prof. Dr. Christoph Wilhelm from the Institute of Clinical Chemistry and Clinical Pharmacology at the University Hospital Bonn, who is also a member of the Immunosensation2 Cluster of Excellence at the University of Bonn. "In contrast, we saw hardly any increase in COVID-19 patients, at least in those with a moderate or severe course."

In addition, it was striking that those infected with the coronavirus had lower levels of inflammatory messengers in their blood. This was particularly true for interferon-gamma. This is a cytokine secreted by a specific group of immune cells, the T-helper cells. These cells use it to summon the help of phagocytes and other defense troops of the immune system to fight viruses. For efficient production of IFN-gamma, however, the helper T cells apparently require an adequate supply of ketone bodies. If this is lacking, they produce less interferon-gamma. In addition, the helper T cells then die earlier.

Ketone bodies make immune system more powerful

The researchers also saw similar effects in another important group of immune cells, the killer T cells. "They, too, need ketone bodies to function well and effectively eliminate the virus," says Dr. Christian Bode, lecturer at the Department of Anesthesiology and Surgical Intensive Care Medicine at the University Hospital Bonn. Apparently, the ketone bodies promote the function of mitochondria, metabolic power houses fueling the immune cells. This not only ensures improved energy production, but also provides molecules that are needed for interferon production.

"Without an adequate supply of ketone bodies, on the other hand, the killer T cells and helper T cells show signs of exhaustion," Bode explains. "In this depleted state, they can no longer perform their function adequately." However, the researchers were able to revive the immune cells by placing diseased mice on a ketogenic diet (a diet low in carbohydrates and protein) or by administering ketone bodies directly. The animals then succeeded better in eliminating the virus and also developed significantly less lung damage.

Hope for new treatment options

The results therefore also raise hope for new treatment options. "It may be possible to increase the power of the body's own defenses through a targeted change in diet," says Wilhelm. "Whether this really works must now be shown by further studies." The researchers expressly advise against self-experimentation with dietary supplements or diets—these could possibly do more harm than good.

The new findings could also be relevant for other infections. In the medium term, they may even contribute to new strategies to help the body fight tumors.
 

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Study finds disparities in United States COVID-19 vaccine distribution
by University of California - San Diego
July 28, 2022

When reports showed that COVID-19 vaccination rates were lower among racial/ethnic minority groups, most discussions focused on mistrust and misinformation among these populations or their reduced access to health care facilities. But new research from University of California San Diego and collaborating institutions has identified an additional barrier to equity: whether or not each health care facility actually received and administered vaccines.

In a study published July 28, 2022 in PLOS Medicine, researchers demonstrated that health care facilities serving underrepresented, rural and hardest-hit communities were less likely to administer COVID-19 vaccines in the early phase of the vaccine rollout.

Led by Inmaculada Hernandez, PharmD, Ph.D., associate professor of clinical pharmacy at Skaggs School of Pharmacy and Pharmaceutical Sciences at University of California San Diego, the study is the first to quantify disparities in the early distribution of COVID-19 vaccines to health care facilities across the country.

Previous studies of vaccine accessibility have not distinguished whether lower access in underserved neighborhoods was a product of the lower concentration of health care facilities in these areas or of inequities in the distribution of COVID-19 vaccines to each health care facility.

To answer this question, Hernandez and colleagues tested whether the likelihood of an eligible health care facility administering COVID-19 vaccines varied based on the racial/ethnic composition and urbanicity of the local county. The team focused on the initial phase of vaccine rollout, using data from May 2021 when states were officially required to make vaccines available to the public.

At that time, 61 percent of eligible health care facilities and 76 percent of eligible pharmacies across the U.S. provided COVID-19 vaccinations. When researchers began comparing these rates with the socioeconomic features of the county in which each facility was located, several patterns emerged.

Facilities in counties with high proportions of Black people were less likely to serve as COVID-19 vaccine administration locations than were facilities in counties with low proportions of Black people. This was particularly the case in metropolitan areas, where facilities in urban counties with large Black populations had 32 percent lower odds of administering vaccines than facilities in urban counties with small Black populations.

Facilities in rural counties and in counties hardest hit by COVID-19 were also associated with decreased odds of serving as a COVID-19 vaccine administration location. In rural counties with high proportions of Hispanic people, facilities had 26 percent lower odds of administering vaccines than facilities in rural counties with low proportions of Hispanic people.

"Both the national policy and public opinion agreed that vaccine distribution should prioritize disadvantaged communities and those hit hardest by COVID-19, but the data shows that is not what happened," said Hernandez.

Further research is necessary to identify the reasons why vaccines were not equitably distributed to all health care facilities and how the involvement of these facilities evolved across subsequent phases of vaccine distribution, the authors said.

"To achieve health equity in future public health programs, including the distribution of booster shots, it is crucial that public health authorities review these early COVID-19 distribution plans to understand how and why this happened," said senior author Jingchuan (Serena) Guo, MD, Ph.D., assistant professor at University of Florida.

Co-authors include Shangbin Tang and Nico Gabriel at UC San Diego, Sean Dickson at West Health Policy Center and Lucas A. Berenbrok at University of Pittsburgh.
 

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Researchers invent accurate rapid COVID-19 antibody level test
by City University of Hong Kong
July 28, 2022

Vaccines have become the most important weapon in the fight against the COVID-19 pandemic, but antibody levels after vaccination decay quickly over time. Therefore, an accurate and affordable antibody rapid test is urgently needed to adjust the revaccination strategy. A research team led by City University of Hong Kong (CityU) recently invented an accurate rapid-testing device that can quantify and display the antibody level as a length of a visual bar, like a mercury thermometer, in as few as 20 minutes, enabling convenient mass screening or individual monitoring of immune protection against COVID-19.

The antibody level is a potent correlate of immune protection against virus infection, but it varies, depending on the vaccine type, and can decay rapidly. In the post-vaccine era, with the rise of the Omicron variants, it is critical to monitor antibody levels in a fast, cost-effective way, which can help provide an alert about the necessity for revaccination. However, existing antibody testing methods are either only for positive/negative results (like rapid antigen tests) or require equipment in professional laboratories or hospitals for quantification, which is expensive, time-consuming and impractical for routine tests.

View: https://www.youtube.com/watch?v=GA-9Z4QyCkc
Procedure for rapid mode of detection. The magnetic microparticles are first mixed with undiluted serum/plasma for five minutes and shaken by hand to capture SARS-CoV-2 antibodies. After rinsing using a magnetic rack to remove the other interfering factors, polystyrene microparticles are added for another five minutes and shaken by hand. Next, the solution is dispensed into the loading chamber of the microfluidic device. After entering the micro-channel, within 10 minutes, an accumulation of polystyrene microparticles is formed that is visible to the naked eye. Credit: Wu., M. et al. / DOI: 10.1126/sciadv.abn6064
1 min 36 sec


A research team led by Dr. Chen Ting-Hsuan, Associate Professor in the Department of Biomedical Engineering at CityU, recently developed a solution by inventing a new rapid antibody test that shows the level of antibodies readable by the naked eye. The findings were published in Science Advances.

Displaying antibody levels in an easily readable way

"There have many attempts to miniaturize conventional immunoassay, such as enzyme-linked immunosorbent assay (ELISA) and electrochemistry, into a portable format. However, these miniaturized immunoassays all need a specific reader to pick up signals, big or small, which is expensive and error-prone if operated by untrained users," explained Dr. Chen. "In contrast, our unique device displays the antibody level directly on the chip, allowing users to see the antibody level by viewing the length of the bar on the chip, making it instrument-free and as easy to read as a thermometer, so it is more suitable for ordinary users."


1659082085159.jpeg
Schematic illustration of the working principle of the new microfluidic device, which directly visualizes antibody levels from COVID-19 vaccines. Both the magnetic microparticles (MMPs) and polystyrene microparticles (PMPs) in the device can bind to antibodies against SARS-CoV-2, but they are based on different mechanisms: the MMPs are coated in the virus's spike protein to ensure specific binding to the antibody against the spike protein, while the PMPs are modified with a secondary antibody against human immunoglobulin G. After loaded into a microfluidic chip, the particle solution first flows through a magnetic separator that removes magnetic microparticles and the connected polystyrene microparticles. At the same time, free polystyrene microparticles continue to flow until they are trapped at a particle dam. Thus, the antibody level is inversely proportional to the accumulative length of polystyrene microparticles, which can be readable and quantifiable by the naked eye without relying on a specific reader. Credit: Dr Chen Ting-Hsuan's Research Team / City University of Hong Kong


The rapid test developed by the team is a finger-sized microfluidic device that contains two types of specially designed microparticles—magnetic microparticles (MMPs) and polystyrene microparticles (PMPs). Both can bind to the antibody against SARS-CoV-2, which is the virus that causes COVID-19. If there are antibodies in the sample, they will bind with both the MMPs and PMPs, forming MMP-antibody-PMP joined microparticles.

Researchers just need to load the particle solution which was mixed with a few small drops of blood plasma collected from a user's finger prick into the microfluidic chip. When the particle solution flows through the chip, a magnetic separator integrated into it removes the MMPs and the joined microparticles. Free PMPs that are not attached to MMPs continue to flow until they are trapped at a particle dam. As the PMPs accumulate, they form a visual bar whose length is inversely proportional to the antibody level in nanograms per milliliter. So it can quantify and visualize the antibody level as a thermometer measures temperature.

The research team tested the detection sensitivity of samples prepared by serial dilution of antibodies and found that the new device could detect antibodies as low as 10.75 ng/ml, which was much more sensitive than conventional rapid tests. More importantly, the detection results of the new device were accurate, as they closely agreed with the results obtained from the gold standard ELISA in a professional laboratory.

Highly sensitive and not easily interfered

The team then tested the detection performance of antibodies in undiluted serum to see whether the complex components within a biological specimen would interfere with the detection performance. The detection level can be adjusted to sensitive mode or rapid mode. Sensitive mode can detect antibodies in a concentration as low as 13.3 ng/ml within 70 minutes. Rapid mode, in contrast, takes only 20 minutes, but the lowest concentration detectable is 57.8 ng/ml.

The team recruited 91 volunteers in Hong Kong with no prior history of COVID-19, who received their second vaccine dose a few weeks before antibody testing. The results revealed that the antibody level reached 1080.8 ng/mL in those who received an mRNA vaccine (BioNTech), which was much greater than the antibody level of 30.2 ng/ml found in those who had received an inactivated vaccine (Sinovac). However, the antibody levels in both groups decayed significantly 45 days after the first measurement. Remarkably, the detection results were highly consistent with the results obtained from ELISA, suggesting the antibody test's high accuracy comparable to the gold standard in professional laboratories.

"Our findings show that our microfluidic rapid test device allows low-cost, fast and accurate measurement of antibody levels by visual inspection, making it particularly suitable for time-saving mass-screening settings and individual use. The new rapid test could be used in local clinics or even testing booths at border entry control points in the future," said Dr. Chen. "This measurement may serve as an antibody-based 'immunity passport' for better evaluation of immune status to accelerate the economic recovery without adding to the medical burden on health care systems. This capability may lead to novel approaches to managing the pandemic in various countries, from zero-tolerance to co-existence with COVID-19."

Dr. Chen and his team are modifying the device to be more accessible and convenient for home use, such as making it capable of detecting antibodies in samples like saliva or nasal secretions.
 

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Study: Vaccines and booster shots are key to controlling spread of COVID variants
by Yale School of Public Health
July 28, 2022

A new study by researchers at the Yale School of Public Health emphasizes the continuing importance of vaccines and booster shots at the individual and population level in controlling infections from highly contagious new variants of COVID-19.

The findings show that not only are vaccinations and boosting important for lowering individual risk of infection, they also aid in controlling COVID-19 within a larger population. With new COVID-19 variants and sub-variants driving current surges in infections, being both vaccinated and boosted is critically important, the researchers said.

"It's not the time to stop getting people boosted. It really makes a huge difference," said Jeffrey Townsend, the study's senior author and a professor of biostatistics and of ecology and evolutionary biology at Yale.

The study appears in PNAS Nexus.

In the study, the researchers used mathematical calculations to determine the likelihood of transmission of the SARS-CoV-2 Omicron variant after an infected person emerges from various lengths of quarantine. The calculations considered the virus's incubation period, incubation time, and test sensitivity in detecting the Omicron variant.

Their results showed that vaccines and booster shots at both the individual and population level are critically important to limiting virus transmission.

"That an individual is recently vaccinated—or even better, recently boosted—substantially decreases their risk of contracting COVID-19," Townsend said. "However, once infected, being recently vaccinated or boosted doesn't change transmission all that much. Therefore, recent vaccination and boosting don't affect the length of quarantine necessary for an individual who is infected with Omicron."

"However, if the population where that infected individual is located is highly vaccinated and boosted, then if that infected individual emerges from quarantine still infected, far fewer people are likely to contract COVID-19 from them," Townsend said. "We concluded, therefore, that within populations where there are high levels of vaccination and boosting, it can be suitable to require quarantines of lower durations and to conduct less frequent testing."

The methods used for the analysis were adapted from a 2020 study in which Townsend and colleagues investigated the transmissibility of the initial SARS-CoV-2 Alpha virus and its impact on quarantine. The researchers were inspired to extend the analytical model and apply it to new data on the Omicron variant in their current study.

"Our concern was with the changes that were going on with the epidemic," Townsend said. "With new variants sweeping through and with higher levels of vaccination and boosting, perhaps the recommendations we made in 2020 can be tailored to these specific circumstances—and they can."
 

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Australian Excess Deaths continue to mount up
Dr Ah Kahn Syed
4 hr ago

Today’s provisional mortality statistics from the Australian Bureau of statistics make for more depressing reading. After 2 years of radical and experimental mandatory public health policy to strive for “zero covid at all costs (but we’re not paying, obv)”…. Australia is now running at 15,572 excess deaths for the year above baseline (9% higher) and 8,308 excess deaths above the 5 year range. Before you ask, the majority of those deaths are from cancer and dementia (aka neglect). As of today, Australia is over 96% vaccinated (adults, i.e. those at risk of dying), and there are over 100 people a week listed as dying of COVID - and rising - making a mockery of those false promises made in 2021.

Remember, many public health “experts” and decision makers have not treated a real patient in years. This democidal disaster is the result of giving them absolute power over individual rights “for your safety”. If this power is not removed from them and given back to the individual it is safe to assume that we can expect more of the same.

1659082745978.png

1659082766543.png
 

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COVID patients in hospital per million, as of July 27th, 2022; UK highest, 2nd Australia, then Canada, Ireland, United States, Denmark, then Netherlands; for ICU, Germany highest, US 2nd
Intensive care has gone down in UK in Omicron but increased in US; why? is it comorbidity issues in US, is is dietary? Look at deaths, it is highest in Australia, then UK, Ireland, Germany, US
Dr. Paul Alexander
1 hr ago


Some graphs to consider:









 

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URGENT: New paper suggests Covid mRNA vaccination rates are linked to increases in overall deaths
Alex Berenson
14 hr ago

Higher use of Covid mRNA shots correlates with a small but notable increase in all-cause mortality, according to a new paper from a Dutch researcher.

The paper draws on Dutch city- and town-level data on vaccinations and deaths to show that areas with high Covid vaccination rates have recently had high rates of all-cause mortality - deaths of all types, Covid or not.

SOURCE

Like many other European countries with high vaccination rates, the Netherlands has had high all-cause mortality for most of the last year, even when Covid deaths are excluded.

(Today, European statisticians reported yet another week of above-normal mortality, with almost 8,000 more weekly deaths than would be expected in midsummer: )

1659083171397.jpeg

A few articles have recently mentioned the trend, although health authorities and most major news outlets continue to ignore it resolutely.


The finding in the new paper is particularly striking because the Netherlands has very high Covid vaccination levels nationally, so the differences between cities are relatively small. Almost every city had vaccination rates between 70 and 90 percent - mostly mRNA shots from Pfizer and Moderna, along with some DNA/AAV vaccines.

The paper found a “vaccination-correlated mortality rate” of about 5 percent of total mortality, meaning that 5 percent of deaths were skewed in patterns that reflected vaccination rates.

As the paper explains, the pattern does not prove that vaccinations actually caused those deaths, merely that the correlation exists. Still, since last summer, highly vaccinated countries have generally posted non-Covid death increases of 5 to 10 percent, the 5 percent figure is far from implausible.

A 5 percent increase in deaths may seem small, but by historical standards it is a huge annual change. It would translate into almost 175,000 extra deaths annually in the United States and more in Europe.

The paper has not been peer-reviewed, and its author, Andre Redert, is a computer scientist, not an epidemiologist (which is arguably a point in his favor). The



Redert finishes his discussion by acknowledging his paper’s “many shortcomings,” including its lack of age-stratified data, but writes:

Our main result remains alarming and calls for more research on the effect of current covid vaccines on all-cause mortality.

Don’t hold your breath.
 

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Does the mystery leading cause of death in Alberta apply to certain age groups?
Nope.
Jessica Rose
19 hr ago

This article is a spin-off of the previous article on Albertans and why they are dying at higher rates than ever before due to “Other ill-defined and unknown causes of mortality”. It’ll be quick and dirty. I found age and gender-stratified cause of death data and plotted the “Other ill-defined and unknown causes of mortality” category for 2019, 2020 and 2021 but this time, I stratified by age. The age groups are quite small so the detail is good.



2021 is the winner in every single age group except for the 5-9ers in 2020, by a long shot. I mean, there are twice as many deaths from this mystery cause in 2021 than for the next highest in 2020 in every single age group. So the bottom line is, this mystery illness is not exclusively killing old people, or young people. Is it killing males more than females? Yes. It is.

Whatever it is.



So what is killing males at twice the rate of females, virtually regardless of age?

Here’s another interesting plot. COVID-19, where the virus was ‘identified’, against the mystery death cause.



Clearly, in 2021, COVID-19 was linked to the elderly with regard to death. But, this mystery killer, affected younger people more. Hmm, could it be that the elderly had already been killed off by the time the mystery killer got to them? What explains something that is killing young people and not old people in Canada, in the age of medicine? And why don’t we know what it is? Are we that lame?
 

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Double Jeopardy: The vaccinated are MORE LIKELY to die with COVID in this province
Hint: The name rhymes with yakisoba
Jestre
5 hr ago

Displayed prominently on Manitoba’s COVID-19 landing page is a figure that claims individuals who are “not fully vaccinated” are six times as likely to be hospitalized with COVID-19, seven times as likely to be admitted to an intensive care unit, and 16 times as likely to die with COVID-19. If it had not been for the last two years of gaslighting, I might have given them the benefit of the doubt.

That update was posted on March 31, they might say.

Things may have changed, they might say.

We forgot to update it, they might say.

Bullshit!

The update looks worse now, but it was a lie at the time, too. According to their own data, between March 1st and March 31st, the unvaccinated were slightly less likely to be hospitalized than the “fully vaccinated” (0.9x) and only slightly more likely to end up in the ICU (1.5x) or die (1.6x). Remember, they claimed on March 31st that the unvaccinated were 16x more likely to die meaning they were off by a factor of 10.



And here is April 1st to April 30th. Hospitalizations remained stable (boosted became more likely to be hospitalized) and deaths looked slightly better for the vaccinated. Still, 2.4-2.5x is a far cry from 16x.



However, things really fell through for the vaccinated in May.



As you can see, the unvaccinated were almost half as likely to die as the fully vaccinated and equally likely to die as the boosted during this period. However, that is not the full story.

Manitoba suffers from the same problem that most other places around the world do. They are using inaccurate population data to calculate their vaccination rates. In short, this leads to highly inaccurate numbers in the elderly population where most of the deaths occur. For new readers, I have done many posts on this phenomenon. See:


This is so widespread that the vaccination rates on the federal health information site decided it would be prudent to obfuscate the data where vaccination rates are above 99%.



Simply put, if they published the real numbers, people might look at the data with more skepticism. They might ask questions. They might catch on.

In Ontario, we found that 675,659 people over the age of 80 had a vaccination. The population of that age group in the data the province used to calculate vaccination rates is 660,520. In fact, the analysts working on the data were well aware of this error.

Months earlier, they had been using 2021 population estimates to calculate vaccination rates; however, in order to artificially shore up vaccine efficacy following omicron, they switched to 2020 population estimates. This was after 2021 population census data became available.

How do we know that they were aware of the problem? Because when they were using 2021 population estimates, they had rates broken down for ages 60-69, 70-79, and 80+. Since it is impossible to calculate rates for a negative population, the province changed the cohorts that they reported rates for. Suddenly, only those 60+ were counted in order to mask the fraud.



The same problem occurs when using age-standardization as Manitoba does. They use 2021 population estimates to calculate their data. The vaccination rate for those 70-79 is 100.25%. Now, can someone answer how you age-standardize for that? What if someone aged 70-79 in the non-existent unvaccinated population dies?

There is another discussion on age-standardization to be had here. I will write a separate article on the topic as it gets more technical and, unfortunately, the Manitoba data has so many lags in the reporting that it is impossible for me to accurately do my own age-standardization on it. However, I suspect they grouped cohorts in the same manner Ontario did. But as you can see above, even using the census 2021 data would remedy the grouping problem.

Yet. That is not the whole story either. While Manitoba has a relatively low growth rate, the distribution of their population is shifting. People are now one year older than in 2021.

Let’s assume that everyone aged by one year. What would their vaccination rate look like then?



In the above chart, I have added a year to both 2021 census and estimate data to reflect this change. I have also assumed the same number of people were born in 2022 as 2021. The latter assumption is almost definitely false given what we have seen with birth rate declines lately, but it is inconsequential as we are only concerned about the older age groups.

As you can see, that changes the entire population dynamic by a enormous amount. In fact, one would not be able to tell we are looking at the same population at all and the vaccination rates for the age groups most likely to die with the virus fall off a cliff.

I can already hear the critic’s voices saying we got you. After all, people in those age groups are dying so we can’t just add a year, right? The thing is most people simply do not die from or with COVID-19. Even a highly effective vaccine makes very little difference in raw death totals. So they may be right that these new populations are lower, but they are missing one key aspect. The vaccinated are dying too. And they have been dying since the vaccination rollout. And we have never taken them off the “vaccine rolls” so to speak.

Meaning, the vaccination rate is already substantially lower than the official rate, and this has never been accounted for. Whereas me adding a year onto the ages in the population only requires I make the assumption that the vaccinated and unvaccinated are dying at similar rates, and if they aren’t, that deaths are rare enough in even these population cohorts that the difference made is nothing more than an error term.

In sum, while Manitoba may want to believe that the fully vaccinated are only dying with COVID at slightly less than twice the rate as the unvaccinated, and the boosted are dying at the same rate, neither is true. Because they are standardizing age using the wrong population denominators, which favor the vaccinated to a high degree, the vaccinated are actually dying at higher rates. And potentially much higher rates.

Sadly, these are things that the so-called “experts” do not flag for people (if they are even aware themselves). They expect those of us watching closely to take numbers greater than 100% at face value.

Yikes.

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Heliobas Disciple

TB Fanatic
(fair use applies)

The Pfizer Paradox: Issues Recall for CHANTIX due to 'theoretical increased risk of cancer' yet its experimental COVID-19 mRNA shots are considered safe?
Sonia Elijah
20 hr ago




I came across a company announcement from Pfizer on the FDA’s website, published on July 19, 2021. I found it quite extraordinary and perfectly paradoxical.

‘Pfizer is voluntarily recalling two lots of Chantix 0.5mg Tablets, two lots of Chantix 1 mg Tablets, and eight lots of a Chantix kit of 0.5mg/1 mg Tablets to the patient (consumer/user) level due to the presence of a nitrosamine, N-nitroso-varenicline, above the Pfizer established Acceptable Daily Intake (ADI) level.

Long-term ingestion of N-nitroso-varenicline may be associated with a theoretical potential increased cancer risk in humans, but there is no immediate risk to patients taking this medication.’


Chantix is a smoking cessation treatment from Pfizer. Their announcement went on to say that nitrosamines, which apparently were present in 12 lots of their tablets and are classified as impurities‘may increase the risk of cancer if people are exposed to them above acceptable levels over long periods of time.’

Most readers will be aware that I’ve extensively investigated Pfizer’s ‘most successful product in history’- it’s COVID-19 mRNA gene therapy ‘vaccine’. Last year, the company made $37 billion in sales and this year its set to make $32 billion- thanks to their booster programme.

Recently, I wrote an investigative report on a series of scandalous leaked EMA emails and Pfizer reports which exposed the fact that just before emergency use authorisation (EUA) was granted, all key regulators (FDA, EMA, Health Canada & MHRA) were made aware that commercial lots of the Pfizer-BioNTech COVID-19 vaccine had ‘visible particles’ and ‘significant loss of mRNA integrity.’ These were ‘major objections’ by the European Medicines Agency (EMA), classifying them as impurities. More importantly, safety and efficacy implications were flagged as being unknown (and they still are).

‘Uncertainties as regards product safety and efficacy of the commercial product’ were again highlighted in a leaked PowerPoint slide used in a meeting between Pfizer and EMA that took place on November 26, 2020. Shockingly, these major objections were ‘resolved’ by simply lowering the standard of the mRNA specification and what about the observed visible particles? I guess, they were just ignored.

Soon after EUA was granted, the global mantra of ‘shots in every arm’ quickly became the order of the day and not just for the elderly or vulnerable but for the very young and healthy- this was against the backdrop of no long-term safety data.

It's hard to ignore (no matter how hard the mainstream media, key regulators, Pfizer and governments try) the skyrocketing number of serious adverse events reported across VAERS, Yellow Card and other vaccine safety monitoring systems around the world, since these experimental COVID-19 ‘vaccines’ were rolled out.

May increase the risk of cancer if people are exposed to them above acceptable levels over long periods of time.This is the reason given by Pfizer for recalling 12 lots of its product, Chantix, perhaps they should consider recalling billions of doses of their gene therapy product- given the mounting number of serious adverse events flooding in.

Exposure (of nitrosamines) over long periods of time, is the main reason stated by Pfizer for issuing its product recall. Yet, neither they nor BioNTech conducted any safety studies (or even planned to) on the accumulated exposure of the novel lipid nanoparticles (through multiple doses) which encapsulate the modified mRNA or the vaccinal spike proteins which continue to be produced in human cells. In fact, Pfizer themselves (such as Pfizer’s rep, Dr Gruber) can’t even answer key scientific questions such as “how much spike protein is being produced in the cells and for how long?”
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Heliobas Disciple

TB Fanatic
(fair use applies)

My Fox News.Com Op-Ed On The President's Vaccine Failure
Double boosted Biden gets COVID, the latest and most public debunking of the narrative "the vaccinated won't get COVID." Vaccine-only prevention has failed, Paxlovid-only early Rx will too.
Pierre Kory, MD, MPA
17 hr ago

Big week of Op-Eds for me and the team! We got one published in the Federalist last week, and we got another one published on FoxNews.com two days ago (included below). I have been informed that foxnews.com is the 3rd most popular website on the internet. Whoa.

I used to be bothered by appearing on news sites with sometimes overt political affiliations. However, as a physician educator living during a historic period of unprecedented levels of scientific censorship, both me and the FLCCC long ago decided to publish and speak to any entity capable of widely disseminating the pragmatic, expert, and evidence-based guidance we have formulated for citizens. Whether you are blue, red, black, or brown etc, we want to help.

Now, Biden getting sick leaves the vaccinators clinging to the last remaining narrative used to combat their Public Enemy #1, that of “vaccine hesitancy” amongst the U.S. population. This last narrative is the famous “you won’t go to the hospital or die from COVID if you are vaccinated.” The original narrative that vaccines protect against disease and spread was ultimately disproven (section 2 in this prior post), but this one is a bit trickier. The only surprising fact about the first false narrative was how long they were able to cling to it using propaganda and absurd chicanery like when the CDC recommended against testing the vaccinated (that one still shocks me in its brazenness). The even greater absurdity is that supposedly legal mandates persist for a vaccine that does not prevent transmission.

Yesterday Biden tested negative and unsurprisingly came out in a victory lap, extolling his administrations efforts against COVID, crediting boosters, at home tests, and the availability of “easy to use” effective treatments from our friends at Pfizer. Absurd misinformation from the nation’s top medical mis-informationist (takes one to know one apparently - wink, wink). He goes on to say, “you can take these pills at home and you can get them from tens of thousands of pharmacies.”
He then follows this with, “the PFDA (the P is not a typo) even put in a special rule so that pharmacists can prescribe the drug!” Pharmacists don’t prescribe by the way (or at least never have in the past). He then exulted, “you don’t even have to go to the doctor!” Note he is referring to the distribution of Pfizer’s Paxlovid, a drug with 120 important drug interactions across 25 different classes of very commonly prescribed medications. It cannot be given concurrently with 75 of them and you have to adjust doses with an additional 29. Even Biden had to be taken off of two of his medications to be treated with it.

I have never in my career used a medication with this many complex drug interactions. Not even close. Yet, now in the U.S it will be “prescribed” by a pharmacist with no more than a superficial knowledge of the chronicity, severity, or treatment history of the patient’s other illnesses. The practice of medicine has been so stellar throughout COVID, this program will assuredly kick it up a notch via this novel direct delivery system of the Pfresident’s (the f is not a typo) pricey new pill. The United States of Pharma is alive and well.

View: https://www.youtube.com/watch?v=K8lkHREnWHw
23 min 50 sec

In the same little speech, he goes on to recommend that all kids over 5 should get vaccinated. Why not include the toddlers while you are at it Joe? I would have loved to be a fly on the wall during his team’s discussion of whether he should just “go for it all” and include the toddlers. I mean the PFDA and CDC unanimously authorized it’s EUA on what is essentially zero evidence to support one (if anything, the trials data, correctly interpreted, indicate negative benefits to toddlers). Yet two large committees, staffed with “Gods of Science and Knowledge” supported a recommendation for use in this age group. Unanimously.

I personally think he didn’t mention toddlers due to the fact that only 2-3% of American parents have brought them in for COVID vaccination. I trust that History will not be kind to this little press conference of misinformation.
So, the vaccinators are now down to their last narrative supporting the vaccines as below (not the one about the vaccinated going to heaven, the one above that).



The “vaccine knowledgeable” minority of the public is small, but the data contradicting this narrative is immense. The U.S is the only country with “official” data to support this assertion, however that data has been so covertly manipulated, almost none of the general public or health system providers are aware of the manipulation nor how it was accomplished.

In previous posts, (here and here), I explored my hypothesis of a systematic and faulty documentation of vaccination status in most U.S hospitals. I recently received further confirmation of its existence. My main front-line nurse source for those two prior posts informed me this weekend that at her academic medical center, she started pointing out to senior nursing colleagues that the majority of patients are listed in the medical record as “unvaccinated” or “unknown” despite the fact that proof of their COVID-19 vaccination is in the chart (albeit buried in a nursing admission note which does not electronically flag them as being vaccinated). It should be noted that no other vaccination was documented in this fashion prior to COVID.

As a result of her “educational” intervention, many senior nurses and nursing directors are now aware of this “glitch.” So much so that it is now openly talked about in staff meetings where nurses and physicians are now being instructed on how to find the actual COVID vaccination status of a hospitalized patient. The reason why staff are so interested in finding out the vaccination status is to better understand the possible causes of the the myriad complex illness presentations they are seeing as well as the increased rates of unprecedented and catastrophic medical emergencies being seen in young, healthy patients ( heart attacks, strokes, aggressive cancers etc). Previously many staff were under the impression that such presentations were due to “long covid”, whereas now they are seeing the truth - that these are the horrible sequelae of COVID mRNA vaccination with lipid nanoparticles.

It is my impression that this systems “glitch” (an investigative journalist I know is trying to find the source of it) compromises the entirety of the U.S hospital data used by the CDC to support this last narrative. Looking at data from countries that did not have this process baked into their electronic medical record-keeping, you find the rates of vaccinated entering hospitals and dying have far exceeded the rates of the unvaccinated for many months now (see Section 3 in this prior post of mine for the data supporting this). The most recent and striking example are the data coming out of New South Wales in Australia showing;
  • Of the 798 COVID deaths in the last 8 weeks, all but 2 were vaccinated
  • Of the 142 deaths in the last week, all were vaccinated, 68% were boosted.
Anyway, on to my Op-Ed where I again, for the millionth time, essentially plead for a more pragmatic and effective approach to the pandemic, one based on an early treatment initiative using safe, repurposed medications. This time I highlighted the evidence for fluvoxamine (had to get off the ivermectin and hydroxychloroquine beat).

Ideally, I think a national campaign of checking every American’s Vitamin D level followed by supplementation strategies to achieve a level above 50 ng/ml for all would have the greatest impact in mitigating the morbidity and mortality of COVID. Maybe I will save that for my next Op-Ed. Enjoy:

OPINION

Published
July 26, 2022 7:00am EDT

Biden's COVID-19 diagnosis is proof vaccines aren't enough to fight virus
Fighting virus requires new tools because vaccines aren't enough and Biden diagnosis is proof
By Pierre Kory

President Joe Biden’s COVID-19 diagnosis is the latest data point showing our government’s "vaccine only" approach needs an immediate course correction. If four doses of a vaccine cannot protect the leader of the free world from infection, it is time to consider other tactics.

These measures should include generic medicines that have been dismissed by the mainstream medical community and media.

While Americans across the ideological spectrum wish the president a speedy recovery, we must take this moment to acknowledge that a strategy blindly focused on vaccinations is not getting the job done.

Don’t take my word for it. Use Biden’s own standard for success. Exactly one year before testing positive, the President declared, "You're not going to get COVID if you have these vaccinations." Back then, the seven-day average of new cases in the United States was around 50,000. Today, that number is estimated to be between 300,000-500,000 when considering ubiquitous and uncounted home testing, despite two-thirds of the population considered "fully vaccinated" by the CDC.

Yet the push for vaccines from the administration has continued unabated. Following Biden’s diagnosis, the White House tried to take a political victory lap. In their first press briefing following news of the diagnosis, White House press secretary Karine Jean-Pierre stressed the president’s vaccination status as, "what’s most important here."

As a lifelong Democrat and medical doctor who has helped more than 700 patients recover from COVID-19 and its complications, I have seen the effectiveness of other treatment options with my own eyes. Take for instance, fluvoxamine, an inexpensive generic medicine typically associated with depression treatment. It costs $4 per pill, is readily available at pharmacies, and has demonstrated an effectiveness combating COVID-19 in large, randomized, controlled trials published in the Journal of the American Medical Association and the Lancet.

Yet two years after this data appeared, fluvoxamine is still getting the cold shoulder from the medical gatekeepers. Both the World Health Organization (WHO) and National Institutes of Health do not recommend its use against COVID-19.
Furthermore, medical professionals who deviate from the party line are callously dismissed by mainstream media outlets such as NPR, as "fringe medical doctors, natural healers and internet personalities ready to push unproven cures for COVID."

Biden working despite having COVID-19, officials say
Video

Science and medicine are always changing for the better. Consider the incredible shifts in the landscape that occurred between the current president contracting the novel coronavirus and his predecessor. In October 2020, there were limited options available for President Donald Trump. Less than two years later, a nearly 80-year-old president was presumed to be on a path toward recovery on the day of his diagnosis.

Progress is a wonderful thing, but it’s only possible with an attitude of open-mindedness that challenges the status quo. Doctors and innovators should be incentivized to pursue and explore new and different approaches. Instead, we are being forced to adopt a group think or risk suffering the wrath of the establishment, or worse, loss of livelihood.

The powerful American Board of Internal Medicine, a sprawling organization with certification authority, has been issuing threatening letters to board-certified physicians with exemplary careers, accusing them of "misinformation" when their public assessments of the efficacy of generic, repurposed therapies contradict those of federal health agencies.

To be sure, demonstrably false "misinformation" can be dangerous, and a topic worthy of discussion. But with overwhelming evidence to support the statements in question, advocating different courses of action toward COVID-19 is far from misinformation. In fact, the suggestion from the White House that the vaccine lessened Biden’s symptoms more closely meets the standard for misinformation since it is an impossible standard to prove.

Of all people, Biden should be open to new ideas. He was elected with a clear mandate to implement a fresh approach toward the pandemic. Two summers ago, he castigated his predecessor, saying, "the president still does not have a plan."
He went on to say, "More than 170,000 Americans have died — by far the worst performance of any nation on Earth."
Today, that number has — sadly — topped 1 million. Many more lives have been lost on this president’s watch than the last one. These are sobering statistics. Biden has fallen short of promise to "shut down" the virus.

It’s clear COVID-19 is going to be with us for the foreseeable future. How we address it is up to us. Now is the time for a change in approach. Let’s hope our elected leaders and medical professionals take heed.

Pierre Kory, M.D., is President and Chief medical officer of the Front Line COVID-19 Critical Care Alliance.
 

Heliobas Disciple

TB Fanatic
(fair use applies)

CanSinoBIO's inhaled COVID booster stronger against BA.1 Omicron subvariant than Sinovac shot
by Roxanne Liu and Ryan Woo
Fri, July 29, 2022, 2:05 AM

BEIJING (Reuters) - Chinese vaccine firm CanSino Biologic's inhalation-based candidate elicited a better antibody response as a booster against the BA.1 Omicron sub-variant than Sinovac's shot, but the antibody level dropped in months, clinical trial data showed.

The result came as top political leaders in China called for proper tracking of virus mutation and developing of new vaccines and treatments in the country's effort to refine its COVID control strategy.

China has given about 56% of its 1.41 billion population a booster dose using domestic shots, and most people were boosted with the same product as their primary series, despite growing evidence that some mix-and-max strategies would likely achieve higher antibody levels.

Among over 100 adults who received a lower dose of CanSinoBIO's inhaled vaccine candidate following two Sinovac shots, after four weeks, 92.5% developed the neutralising antibody that neutralises Omicron at levels that researchers defined as detectable, according to a paper published without peer review.

That compared with 88.9% for a higher-dose group, also with over 100 participants, said in a paper published late on Thursday.

The rate for both groups declined to around 70% after six months of the inhaled booster.

Barely any of the over 100 participants who received a third Sinovac shot had detectable neutralising antibody for Omicron after four weeks or six months.

The study did not compare CanSinoBIO's inhaled booster with other potential boosters that have triggered stronger antibody responses than a third dose of the Sinopharm or Sinovac shot.

Antibody-based readings reflect an important part of the vaccine-triggered immune response, and are different from the vaccine efficacy that indicates how well a shot reduces the risk of COVID disease, hospitalization or death.

The impact of BA.4 and BA.5 Omicron sub-variants on CanSinoBIO's inhaled vaccine deserves further study, said the authors, who worked at CanSinoBIO and other Chinese institutes.

CanSinoBIO's experimental inhaled vaccine uses a technology similar to that of its injection-based shot, which has been approved in countries including China, Mexico and Argentina, and AstraZeneca's vaccine.

The company is also testing a candidate based on the mRNA method in a mid-stage clinical trial in China.
 
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