CORONA Main Coronavirus thread

marsh

On TB every waking moment

marsh

On TB every waking moment
Thank you, Marsh, for your indefatigable efforts to keep us all informed of this scourge. You have helped more than just us, but also our extended families and friends. Wishing you all the best and hope that in 2022 you will feel that you can rest from this challenge.
Thanks Pinecone. I hope so too.
 

marsh

On TB every waking moment
View: https://www.youtube.com/watch?v=OM2VgBm9pTI
20:51 min

Most omicron hospitalisations incidental

Dec 29, 2021


Dr. John Campbell


Around 80% of English hospital admissions with coronavirus are admitted for other reasons UK, 24th December Omicron hospital patients, 366 Total omicron deaths, 29 UK, 27th December Omicron hospital patients, 407 Total omicron deaths, 39 Omicron cases + 45,307 = 159,932 UK, 29th December Omicron hospital patients, + 261 + 98 = 766 Total omicron deaths, + 10 + 4 = 53 UK data https://www.gov.uk/government/publica... https://covid.joinzoe.com/data#levels... https://coronavirus.data.gov.uk

SA data SA hospital data https://www.nicd.ac.za/diseases-a-z-i... https://www.worldometers.info/coronav...

US cases and deaths data https://covid.cdc.gov/covid-data-trac... Isolation down to 5 days is asymptomatic 20% of covid admissions caused by viral complications https://www.telegraph.co.uk/news/2021...

December 21, England Covid patients in hospital = 6,245 Up 259 from previous week Of the 259, just 45 admitted because of the virus Of the 259, admitted, 214 for other conditions but having also tested positive “incidental Covid” admissions Previous week, December 7 to December 14 Majority of hospitalisations were still delta Primary covid cases were 59% of the 289 weekly rise

People currently in hospital with Covid “incidental” cases, 1,813 out of 6,245 Highest so far Sir John Bell, regius professor of medicine, Oxford University

This is not the same disease we were seeing a year ago The horrific scenes that we saw a year ago – intensive care units being full, lots of people dying prematurely – that is now history in my view and I think…that’s likely to continue

Chris Hopson, the chief executive of NHS Providers What our guys are saying is that incidental cases are making around 25 to 30 per cent of cases that are arriving, but that will vary from place to place In London you would expect to see higher levels lower in somewhere like the South West, where community infections are lower They are seeing an increase in the number of hospital admissions but it's not precipitous. It's not going up in an exponential way

As the number of cases in the community rises, there are significant levels of incidental cases But we mustn't forget that having those people in hospital causes complications because of infection control measures under significant amounts of pressure and are struggling with high numbers of staff absences More cases of incidental Covid compared to previous waves

Dr Raghib Ali, consultant in acute medicine at Oxford University Hospitals,
There is certainly a smaller proportion of people ending up with Covid pneumonia in intensive care Probably half the cases I’ve seen are incidentals You’ve got completely incidental cases, someone coming in with a broken leg, who also tests positive for Covid, then a third category of older people who have comorbidities. Maybe they’ve had a fall or chest pain and also test positive and it's unclear if the virus is having some sort of impact. And when the prevalence of a virus with relatively mild symptoms is high in the community then you will see higher incidentals Similar to Gauteng, with 52% incidentals Report from Intensive Care National Audit and Research Centre (May 1 to Dec 24) https://www.dailymail.co.uk/news/arti... https://www.icnarc.org/our-audit/audi...
 

marsh

On TB every waking moment

HUGE. CDC Withdraws Use of PCR Test for COVID and Finally Admits the Test Can Not Differentiate Between the Flu and COVID Virus

By Jim Hoft
Published December 29, 2021 at 9:10am
cdc-SARS-alert-.png


This is BIG NEWS.
After December 31, 2021, the CDC will withdraw the emergency use authorization of the PCR test for COVID-19 testing. The CDC finally admitted the test does not differentiate between the flu and COVID virus.

Via the CDC website:
In preparation for this change, CDC recommends clinical laboratories and testing sites that have been using the CDC 2019-nCoV RT-PCR assay select and begin their transition to another FDA-authorized COVID-19 test. CDC encourages laboratories to consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses. Such assays can facilitate continued testing for both influenza and SARS-CoV-2 and can save both time and resources as we head into influenza season.
This explains the disappearance of Flu cases in the US in 2020. It also inflated the COVID cases as Dr. Fauci and the DC elites knew would happen.

Via Europe Reloaded:
QUIETLY WITHOUT MEDIA ATTENTION, THE CENTERS FOR DISEASE CONTROL AND PREVENTION (CDC) HAS WITHDRAWN THE PCR PROCESS AS A VALID TEST FOR DETECTING AND IDENTIFYING SARS-COV-2.
“After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only.”

The CDC admits that the PCR test cannot differentiate between SARS-CoV-2 and influenza viruses.

I reported several months ago that the “health authorities” had reached this decision but were withholding its implementation until the end of 2021. They needed the fake test to keep the fear going in order to achieve as much vaccination, and therefore as much profit, as possible.

It is extraordinary that the CDC’s withdrawal of the test received no attention from the media or politicians.

Dr. Kary Mullis, Nobel Laureate and inventor of the PCR process said several years ago that “the PCR is a process. It does not tell you that you are sick.” It was never meant to be a Covid test.
 

marsh

On TB every waking moment

CDC Director Walensky Says Testing at the End of Quarantine No Longer Needed Because PCR Tests Can Stay Positive For Up to 12 Weeks (VIDEO)

By Cristina Laila
Published December 29, 2021 at 11:44am
FHx6GWjXsAgBRTs.jpg

Rochelle Walensky

CDC Director Rochelle Walensky on Wednesday said testing at the end of quarantine is no longer needed because PCR tests can stay positive for up to 12 weeks.

The CDC has known about the faulty PCR tests from the beginning but they used the tests to destroy the economy and unseat Trump.

After December 31, 2021, the CDC will withdraw the use of the PCR test for COVID-19 testing. The CDC finally admitted the test does not differentiate between the flu and COVID virus.

This explains the disappearance of Flu cases in the US in 2020. It also inflated the COVID cases as Dr. Fauci and the DC elites knew would happen.

Walensky finally admitted what we have known to be true for nearly two years: Faulty PCR tests plus long quarantine times have created a “casedemic.”

“So, what we do know is the PCR test after infection can be positive for up to 12 weeks so that is not going to be helpful,” Walensky said Wednesday on “Good Morning America.”

She continued, “You’re not going to be transmitting during all of that period of time. We’ve seen that in study after study.”

Walensky also admitted the antigen test people were taking five days after Covid infection was faulty and therefore no longer needed.

VIDEO:

View: https://twitter.com/i/status/1476168350711623691
4:42 min

A quick recap of the CDC’s sudden shift in the last 48 hours after Biden said “there is no federal solution to Covid”:
  • The CDC was wrong about Omicron and they suddenly shifted their guidelines on quarantine times in just a matter of 24 hours.
  • The CDC on Monday recommended shorter Covid isolation and quarantine time for all Americans.
  • The CDC made the decision to cut isolation time from 10 to 5 days in an effort to help Joe Biden and make sure there isn’t a total collapse of society under his watch.
  • The CDC withdrew the use of PCR tests for Covid and finally admitted the test cannot differentiate between Covid and the flu.
  • The CDC also admitted testing at the end of isolation is no longer needed because the PCR and antigen tests are faulty.
What else is the CDC lying about for political reasons?
 

marsh

On TB every waking moment

Biden Regime “Actively Preventing” Life-Saving Monoclonal Antibody Treatments to Florida and Texas

By Jim Hoft
Published December 29, 2021 at 12:08pm
IMG_5431.jpg


Florida Surgeon General Joseph Ladapo accused the Biden administration of “actively preventing” the delivery and distribution of life-saving monoclonal antibody treatments to the Sunshine State.

1640820572966.png


Back in September Governor DeSantis slammed the Biden regime for slashing monoclonal antibody treatments to Florida. The regime would rather see people die than give DeSantis and Florida more good press.

Jen Psaki defended the unconscionable decision at the time.


1640820490901.png

FOX News reported:
Florida Surgeon General Joseph Ladapo accused the Biden administration of “actively preventing the effective distribution of monoclonal antibody treatments” in the United States, according to a Tuesday letter addressed to Secretary of Health and Human Services Xavier Becerra.

The Biden administration recently paused shipments of COVID-19 antibody treatments manufactured by major drug companies Regeneron and Eli Lilly amid claims that such treatments are not effective against the omicron variant of the coronavirus.



The federal government continues to supply Sotrovimab, a monoclonal antibody from the company Glaxosmithkline, which reportedly does work against omicron.
They have also stopped shipments to Texas.

These people are evil.

1640820430644.png
 

marsh

On TB every waking moment

Fauci Moves Goalposts Again, Says Shutting Down the Country is Bad For People’s Health (VIDEO)

By Cristina Laila
Published December 29, 2021 at 2:00pm
IMG_8657.jpg

Dr. Fauci moved the goalposts again as the CDC shifts policies to help Joe Biden and the Democrats going into 2022.

The CDC suddenly updated its Covid guidelines and took into consideration the economic impact that long quarantine times and forced isolation has on society.

A quick recap of the CDC’s sudden shift in the last 48 hours after Biden said “there is no federal solution to Covid”:
  • The CDC was wrong about Omicron and they suddenly shifted their guidelines on quarantine times in just a matter of 24 hours.
  • The CDC on Monday recommended shorter Covid isolation and quarantine time for all Americans.
  • The CDC made the decision to cut isolation time from 10 to 5 days in an effort to help Joe Biden and make sure there isn’t a total collapse of society under his watch.
  • The CDC withdrew the use of PCR tests for Covid and finally admitted the test cannot differentiate between Covid and the flu.
  • The CDC also admitted testing at the end of isolation is no longer needed because the PCR and antigen tests are faulty.
CDC Director Walensky on Wednesday said the decision to update Covid guidelines was in part due to making sure society doesn’t collapse.

Fauci moved the goalposts, defended the CDC’s new guidelines and said lockdowns are bad for people’s health.

“When you shut down society, when you shut down the country, there’s a lot of deleterious effects that go along with that, that go well beyond the economy — the availability of people to get things done for their own health,” Fauci said.

He continued, “When you shut down the country, you have people who have other diseases who don’t have the opportunity to get their HIV tests, to get their HIV meds to get their mammograms, to get their colonoscopies — all the things you do — when you shut down, there’s a lot of deleterious effects that go well beyond the economy…”

So now it’s okay to have this point of view?

Anyone who said exactly what Fauci just said was called a “grandma killer” for the past year-and-a-half.

VIDEO:
View: https://twitter.com/i/status/1476263246587994115
.36 min
 

marsh

On TB every waking moment

Fauci ‘Strongly’ Warns Against Hugging and Kissing on New Year’s Eve

By Cassandra Fairbanks
Published December 29, 2021 at 2:27pm
fauci-border-crossers-checked.jpg


Dr. Anthony Fauci is “strongly” warning against hugging and kissing your friends and loved ones on New Year’s Eve this year.


Fauci also told people to avoid large gatherings during the White House COVID-19 briefing on Wednesday.

“If your plans are to go to a 40- to 50-person New Year’s Eve party with all the bells and whistles and everybody hugging and kissing and wishing each other a happy new year, I would strongly recommend that this year we do not do that,” Fauci said.

View: https://twitter.com/i/status/1476265895014109184
1:02 min

Instead, he told people to have smaller gatherings with people who are “boosted.”

“If you were in a situation with a family setting, in your home, with family—parents, children, grandparents—and everyone is vaccinated and boosted, although the risk is never zero in anything, the risk is low enough that we feel you should continue to go through with those plans of having a home-related, vaccinated, boosted gathering with family and close friends who are also vaccinated and boosted,” Fauci said.

“So, it really depends on what your plans are,” he added.
 

marsh

On TB every waking moment

Global New Cases Top 1 Million For 2nd Day, Paris Requires Masks Outside

WEDNESDAY, DEC 29, 2021 - 03:49 PM

Update (1545ET): The French government has continued to tighten restrictions on the public, driven by the rising wave of infections.

In Paris, the people will need to wear masks in public even when they are outdoors. The new restriction will start Dec. 31.

The decision comes after the government reported more than 200K new cases, following roughly 180K the prior day. The information was attributed to French Health Minister Olivier Veran.
* * *

Update (0845ET): CDC chief Dr. Rochelle Walensky said during an interview on Wednesday that the agency is making progress on providing boosters for children. The FDA is currently looking at boosters for children between 12 and 15, and the CDC will "act swiftly" once the FDA approval is granted.

Boosters for minors in the 12-15 age group likely won't be approved within the next month. But the scientists are "getting there."

As for all this talk about requiring vaccines for domestic travel? It's not going to happen, she said.

Confused? Well, let's clear things up:

Fauci: travel vax mandate is on the table...

Fauci next day: no travel vax mandate

Biden day after that: travel vax mandate will happen when docs say

Yesterday late CDC Walensky: no travel vax mandate being discussed
Walensky also claimed the US is seeing a growing number of kids in hospitals.

She also provided some clarity on the latest CDC guidelines. Those who are exiting quarantine no longer need a PCR test showing they are negative because some people can stay negative for as long as 13 weeks after infection. "So we would have people in isolation for a very long time if we were relying on PCRs," she said.

Walensky also addressed Tuesday's news from the FDA that, according to early data, rapid antigen tests may be less sensitive when it comes to the omicron variant. "We do know that the most sensitive test you can do is a PCR test...So if you have symptoms and you have a negative antigen test, we do ask you to go and get a PCR to make sure those symptoms are not attributable to COVID."

However, she added, the rapid tests work "quite well" especially in environments where people are tested frequently, like schools. "They may not work as well as they have for the delta variant...we still are encouraging their use," Walensky said.
* * *

Since seemingly everybody in the US either knows somebody who is sick, or is sick themselves, millions of Americans are about to start loudly questioning why they bothered to get three shots if it wasn't enough to stop them from eventually getting sick.

Many assumed this latest wave was all omicron, but as we reported last night, the CDC has lowered its estimate for omicron's prevalence from 70%+ all the way down to 59%. That's the percentage of sequenced COVID cases that were confirmed to omicron during the past week.



It looks like Dr. Fauci is going to have a lot more explaining to do.

Globally, the number of newly confirmed COVID cases topped 1M for a second straight day as the hyper-infectious omicron has helped to drive the latest seasonal wave.

As a result, countries are tightening restrictions on international travel targeted at Americans, while Dr. Fauci exhorts Washington to respond with restrictions on domestic travel for all Americans, along with more restrictions on foreigners traveling to the US, per BBG.

The Netherlands will now require travelers arriving from the US to self-quarantine for up to ten days.

Hospitalizations are spiking from New South Wales to New York State (although Australia is still nowhere near the level of virality seen in the US).

As cases surge to record levels down under, the Australian government is scrambling to change its testing rules to clear up congestion at test sites.

Their problem isn't so different from what's happening in the UK and the US, per Reuters.
Prime Minister Scott Morrison said on Wednesday Australia needed "a gear change" to manage overburdened laboratories and get people out of isolation. He called a snap meeting of the national cabinet on Thursday.
"We just can't have everybody just being taken out of circulation because they just happen to be at a particular place at a particular time," Morrison said during a media briefing.
Morrison's plan would prioritize urgent cases while relying more on rapid antigen tests, which are being used in the US.

Since cases are surging, omicron has proven it has a lower hospitalization rate than previous variants. The only problem is that with so many new cases, inevitably, there are going to be more hospitalizations as well.

Elsewhere, the government of Tokyo confirmed 76 new coronavirus cases in the capital on Wed., the most since Oct. 9 (although the number of serious cases dropped from 2 to 1).

Here's some more COVID news:
  • Malaysia has become the latest country to lift a travel ban on the eight south African countries that the US also imposed restrictions upon after the discovery of omicron.
  • Vietnam plans to initially limit the resumption of regular international flights to routes between the Southeast Asian country and Japan and the U.S. in early January.
  • More than 1.2 billion Chinese people, or about 86% of the country’s population, were fully vaccinated as of Dec. 28, an official at the National Health Commission said during a briefing on Wednesday. Some 465M doses were administered to minors aged 3 to 17.
  • India is stepping up defenses against a possible third wave of coronavirus infections caused by omicron by implementing a slew of measures, including approving two more vaccines as well as Merck's COVID-19 pill, and expanding its inoculation drive to those aged 15 to 18.
  • In the UK, a sharp rise in NHS staff absences due to sickness because of COVID is threatening to hamper patient care, health leaders have warned, as the number of hospitalizations in England hit the highest level in 9 months.
And as we reported yesterday, France has decided to require more people to work from home. As for when the winter wave might peak, scientists are looking to last year's wave, and estimating that the surge in cases will peak some time between early January and early February.
 

marsh

On TB every waking moment

Mexican Government Allowing Cruise Ships With COVID-19 To Disembark

WEDNESDAY, DEC 29, 2021 - 03:25 PM
Authored by Katabella Roberts via The Epoch Times,

Mexico will allow cruise ships carrying people infected with COVID-19 to dock, the country’s government announced on Tuesday.


In a news release, the government said it will allow passengers who show symptoms of the virus, also known as SARS-CoV-2, to disembark but they must quarantine. Those who test positive will be provided with medical assistance.
“In accordance with the biosafety protocols established in the national and international spheres, the Government of Mexico will receive in its maritime ports cruise ships that request to dock in our country,” they said in a statement.
Asymptomatic people or those with a mild condition will be kept in preventive quarantine, while individuals who present serious symptoms will be treated in the hospitals of the cities where they disembarked.

Passengers or crew who do not show symptoms of COVID-19 will “enjoy free transit” but must follow preventative measures such as wearing face masks, regularly washing hands with soap and water, or using 70 percent alcohol-gel, and maintain a “healthy” social distance.

The release also said that a cruise ship that was recently denied entry to a Mexican port would be allowed to dock but did not provide further details as to which cruise ship it was referencing.

The Mexican state of Jalisco’s health department confirmed in a statement to media outlets on Dec. 29 that 21 crew members onboard the Koningsdam cruise line tested positive for the virus when it arrived in the tourist resort city of Puerto Vallarta over the weekend.

Holland America confirmed in a statement on Saturday to news outlets that a “small number of fully-vaccinated crew on Koningsdam tested positive for COVID-19.”
“All are showing mild or no symptoms and are in isolation. Close contacts have been quarantined out of an abundance of caution,” the cruise line said.
According to the Jalisco health department, all crew members were tested for COVID-19 prior to departure on Dec. 19 and just one person tested positive for the CCP (Chinese Communist Party) virus, which causes COVID-19.
“Regarding a cruise ship that was denied access in two maritime ports of our country, it is reported that it will be received in the port of Guaymas, Sonora, with the support of the government of that entity,” the Mexican government said on Tuesday.
“The Secretaries of Health and Tourism of the Government of Mexico reiterate the commitment to respect the provisions of the International Health Regulations of the World Health Organization (WHO), for which cruises will be received in ports maritime of the country,” the release continued.

“Our country maintains its policy of solidarity and fraternity, as well as the principle of non-discrimination towards all people, so the health and tourism authorities remain pending to provide necessary medical assistance to those who visit us for recreational, work, commercial reasons, and academics, among other activities, carried out in compliance with national laws,” the release said.
Mexico is one of the few countries in the world that has not implemented travel bans, testing requirements, or mandatory face mask wearing for visitors.

The country’s deputy health secretary, Dr. Hugo López-Gatell Ramírez, said on Nov. 27 that travel restrictions and border closures in response to the recently discovered Omicron variant of the virus are “unhelpful measures” that will affect the economy and well-being of the people.
“It [Omicron variant] has not been shown to be more virulent or to evade the immune response induced by vaccines,” Ramírez said last month.
According to data from the World Health Organization (WHO), there have been 298,777 deaths from the CCP virus in Mexico. Some 138,851,637 vaccine doses have been administered.
 

marsh

On TB every waking moment

Rand Paul: Thousands Dying Every Month Because Of Fauci's Obsession With Pushing Vaccines

WEDNESDAY, DEC 29, 2021 - 08:25 AM
Authored by Steve Watson via Summit News,

Senator Rand Paul has warned that thousands of Americans are dying from COVID every month because Anthony Fauci is obsessed with pushing vaccines in place of therapeutic treatments that are effective in treating the virus.



Appearing on his Father Ron Paul’s Liberty Report, the Senator noted that Fauci has displayed a bias toward vaccines since he attempted and failed to produce a vaccine for AIDS and HIV in the 1980s and 90s.

“I would venture to say that thousands of people die in our country every month now because [Fauci] has deemphasized the idea that there are therapeutics,” Paul urged.

View: https://twitter.com/i/status/1475546540060069893
2:14 min

“Because he’s made this mistake of de-emphasizing natural immunity, I think thousands of people have lost their lives,” the Senator continued, adding “For instance, I’ve already had it [Covid-19] I should be at the end of the line.”

“Many older people die, and many 35-year-old people are being vaccinated, that makes no scientific sense,” Paul emphasised.

Ron Paul then asked his son if he believes the pandemic was brought about as part of a conspiracy.

“Do you think there was a plan to bring this about, and Fauci was there, and part of the plan with Gates, or do you think something was happening at a more modest rate and they jumped on it and twisted it and made a big deal of it?” the Senior Paul asked.

Rand Paul responded “So the pandemic comes, there’s this natural worry media plays up worry, because it sells,” adding “I would call it less of a conspiracy and more of a philosophy.”

“I think Fauci is of the philosophy that vaccines are incredibly successful and are the way to go versus therapeutics, for example.”

“I blame Dr. Fauci because he was never on TV saying if you get sick there is a treatment,” Paul explained, adding “Because it’s everything about the vaccine, and if you’re not vaccinated you’re unclean. You’re like a leper.”

Watch the full interview below:

View: https://youtu.be/hpkVxD661y0
28:15 min
 

marsh

On TB every waking moment

COVID-19 Will Become "Just Another Cause Of Common Cold": UK Professor

WEDNESDAY, DEC 29, 2021 - 06:30 AM
Authored by Alexander Zhang via The Epoch Times,

COVID-19 will become “just another cause of the common cold” and people who test positive will have to be allowed to go about their normal lives as they would do with any other cold, a British medical professor has said.


Paul Hunter, professor in medicine at the University of East Anglia, told BBC Breakfast on Dec. 28:
“COVID is only one virus of a family of coronaviruses, and the other coronaviruses throw off new variants typically every year or so, and that’s almost certainly what’s going to happen with COVID—it will become effectively just another cause of the common cold.
Hunter said that, at some point, the daily reporting of COVID-19 case numbers will no longer be warranted.
“We’re not going to be doing daily reporting on cases of the different causes of the common cold going forward, of which COVID is one,” he said, adding that restrictions could be scaled back once the Omicron variant has been dealt with, possibly after Easter.
Hunter said:
“We’re going to have to let people who are positive go about their normal lives as they would do with any other cold."
He said the self-isolation rules will have to be relaxed at some point, because “this is a disease that’s not going away.”

UK Health Secretary Sajid Javid confirmed on Dec. 27 that no further CCP (Chinese Communist Party) virus restrictions will be introduced in England, at least before the new year.

Environment Secretary George Eustice said on Dec. 28 that, though infection rates from the new Omicron variant are rising, there was evidence it was not resulting in the same level of hospital admissions as previous waves.

“There is early encouragement from what we know in South Africa that you have fewer hospitalisations and that the number of days that they stay in hospital if they do go into hospital is also lower than in previous variants,” he told the BBC Radio 4 Today programme.
“At the moment we don’t think that the evidence supports any more interventions beyond what we have done,” he said, adding that the government keeps it “under very close review.”
Also talking to the Today programme, Professor Sir John Bell, regius professor of medicine at Oxford University, backed the government’s decision not to impose new restrictions.

“The horrific scenes that we saw a year ago—intensive care units being full, lots of people dying prematurely—that is now history in my view and I think we should be reassured that that’s likely to continue,” he said.
 

marsh

On TB every waking moment

How COVID Lockdown Fanatics Took Over The World

WEDNESDAY, DEC 29, 2021 - 03:30 AM
Authored by Jeffrey Tucker via The Brownstone Institute,

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

Now I was listening.

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

He literally unleashed hell.



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

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

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

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

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

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

Fat chance. His greatest fears have been realized. The movement against what he did is now global, ferocious, and insuppressible. It’s not going away. It is only going to grow, despite his best efforts.

This is how it has been for the better part of the last 21 months, with social media and YouTube deleting videos that dissent from lockdowns. It’s been censorship from the beginning. Now we see what happens: the lockdowns have birthed a new movement plus a new way of communicating plus new platforms that are threatening monopoly control the world over. Not only that: political and economic upheaval seem inevitable.

For all the problems with Lewis’s book, and there are plenty, he gets this whole backstory right. Bush came to his bioterrorism people and demanded some huge plan to deal with some imagined calamity. When Bush saw the conventional plan — make a threat assessment, distribute therapeutics, work toward a vaccine — he was furious.
“This is bulls**t,” the president yelled.
“We need a whole-of-society plan. What are you going to do about foreign borders? And travel? And commerce?”
Hey, if the president wants a plan, he’ll get a plan.
“We want to use all instruments of national power to confront this threat,” Venkayya reports having told colleagues.
“We were going to invent pandemic planning.”
This was October 2005, the birth of the lockdown idea.
Dr. Venkayya began to fish around for people who could come up with the domestic equivalent of Operation Desert Storm to deal with a new virus. He found no serious epidemiologists to help. They were too smart to buy into it. He eventually bumped into the real lockdown innovator working at Sandia National Laboratories in New Mexico.

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

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

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

Glass imagined himself to be smarter than 100 years of experience in public health. One guy with a fancy computer would solve everything! Well, he managed to convince some people, including another person hanging around the White House named Carter Mecher, who became Glass’s apostle.
Please consider the following quotation from Dr. Mecher in Lewis’s book:
“If you got everyone and locked each of them in their own room and didn’t let them talk to anyone, you would not have any disease.”
At last, an intellectual has a plan to abolish disease — and human life as we know it too! As preposterous and terrifying as this is — a whole society not only in jail but solitary confinement — it sums up the whole of Mecher’s view of disease. It’s also completely wrong.

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

Jump forward to March 12, 2020. Who exercised the major influence over the decision to close schools, even though it was known at that time that SARS-CoV-2 posed almost no risk to people under the age of 20? There was even evidence that they did not spread COVID-19 to adults in any serious way.

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

Based on the timestamp and length of the emails, Mecher was clearly not sleeping much. Essentially he was Lenin on the eve of the Bolshevik Revolution.

How did he get his way?

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

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

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

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

marsh

On TB every waking moment

A Perfect Storm Of Incentives

TUESDAY, DEC 28, 2021 - 11:00 PM
Authored by Antony Davies via The American Institute for Economic Research,

It is not yet clear whether history will remember the 2020s more for an outbreak of a deadly virus, or for an outbreak of mass psychosis.

No doubt, both were at play, the former because the virus was novel and deadly, the latter because we had no idea how much so. In March of 2020, the World Health Organization estimated Covid’s case fatality rate to be over 3 percent.

Some outlets reported case fatality rates above 10 percent. By comparison, the case fatality rate for the common flu is a mere fraction of a percent.

But the early information ranged from sketchy to biased. In the early days, the number of Covid tests was limited, so physicians only tested those who were sick enough to show up at hospitals. This skewed the early data toward showing Covid as being deadlier than it actually was. With no randomized testing, the actual lethality was impossible to know.

This bias interacted with the media and politicians’ incentives to create a perfect storm of incentives.


The media had an incentive to repeat the worst fatality projections and to play down the bias behind the projections because bad news attracts viewers, and viewers attract advertising dollars. Heavy media coverage of the worst Covid projections alarmed voters, and that forced politicians to respond.

But the politicians’ incentives were skewed toward a heavy-handed response.

There were two ways politicians could have been caught making mistakes.

Politicians might not have imposed lockdowns when lockdowns were needed. If they erred in this way, the error would have become quickly and clearly evidenced in body counts. Angry voters would have looked for someone to blame, and the politicians would have been the clear choice. Conversely, politicians might have imposed lockdowns when lockdowns were not needed. If they erred in this way, the error would have remained mostly hidden.

Unemployment and business closures would skyrocket, but politicians could point to the millions of hypothetical deaths that “would have occurred” were it not for the lockdowns.

By late 2020, it became clear that early case fatality rates were overstated, but it was too late for politicians to change course. A feedback loop had ensued wherein the media sold advertising by spotlighting the Covid danger.

This made people fearful, and the people pushed politicians to act. Politicians acted and then hid the potential error of unnecessary lockdowns by emphasizing the danger of Covid. This gave the media more material to spotlight and more advertising to sell. Social media then jumped into the fray by anointing itself the arbiter of what was and wasn’t “misinformation.” But social media was as motivated as the mainstream media to attract eyeballs and sell advertising, and so anything that contradicted the official line on Covid was deemed “misinformation.”

The result was mass psychosis in which people’s behaviors toward the real threat of Covid became inconsistent with their behaviors toward other real threats. And what was the real threat of Covid?

While most countries imposed lockdowns, Sweden resisted. The Swedish government recommended social distancing and banned gatherings of more than 50 people, but it did not require businesses to close. Because of differences in population mobility, density, size, and the environment, a comparison of Sweden to the United States isn’t possible. What is possible is a comparison of Sweden to Sweden. The Imperial College of London (ICL) produced the early forecasts of Covid deaths. These were the forecasts on which politicians based their policy decisions. Applying the ICL forecast model to Sweden, Swedish epidemiologists predicted that, by July 1 2020, Sweden would have suffered 96,000 deaths if it had done nothing, and 81,600 deaths with the few policies that it did employ. In fact, by July 1, Sweden had suffered only 5,500 deaths.

The ICL model overestimated Sweden’s Covid deaths by a factor of nearly fifteen.

Early ICL forecasts indicated that, unchecked, Covid would kill 40 million worldwide in 2020, and that the number could be cut in half by social distancing and isolating the elderly. According to the World Health Organization, worldwide Covid deaths for 2020 totaled 1.8 million.

The ICL model overestimated world Covid deaths by a factor of ten.

For 2020, the same ICL forecasting model also predicted that, if the countries did nothing in response to Covid, up to 2.2 million people in the US and another 550,000 in the UK would directly die from Covid.

Suppose that ICL predictions of US and UK Covid deaths were overstated only by a factor of three. Then, in the absence of lockdowns and mandatory masks, the United States could have expected around 730,000 Covid deaths and the UK 180,000 in 2020. How many people actually died? In 2020, the number of direct deaths due to Covid were approximately 360,000 in the US and 77,000 in the UK.

Thus, even assuming that the ICL model had a significantly smaller bias than it demonstrated elsewhere, the lockdowns appear to have only saved around 370,000 lives in the US and 103,000 in the UK.

To further skew these estimates, the ICL model assumes nonpharmaceutical interventions only. The widespread availability in the US of a vaccine, beginning in mid-2020, further reduces the number of lives the lockdowns saved. In short, however many lives the lockdowns did save, they were far fewer than what the ICL models predicted they would save.

As with all things, lockdowns do not come without tradeoffs. Some people died of cancer, kidney disease, and other non-Covid causes because they were afraid to go to hospitals out of fear of contracting Covid. In Canada, cancer screening was suspended so that hospital resources could be devoted to Covid care. Early estimates show up to a 10 percent increase in cancer deaths as a consequence. In the US in the early days of Covid, there was a 30 percent decline in the number of people seeking initial treatment for kidney disease.

At the start of the pandemic, calls to suicide hotlines spiked across the country, as did instances of domestic violence. The Centers for Disease Control estimates that the total number of deaths in the US was 450,000 larger than it should have been in 2020. That 360,000 of those were directly due to Covid means that the remaining 90,000 were due to Covid only indirectly or due to the lockdowns themselves.

In addition to the lockdowns costing lives, we expended unprecedented resources maintaining them. These came initially in the form of unemployment and business closures, and later in the form of supply chain problems and inflation and higher taxes to pay for massive stimulus spending. In late 2020, economists estimated that, provided it ended by the fall of 2021, the pandemic will cost the United States around $16 trillion over the next decade. That’s around $40 million for every life saved.

But how many more lives might we have saved had we done something different with those resources? Around 660,000 people die each year of heart disease in the US. The National Institutes of Health spends around $5 billion each year researching cures for cardiovascular diseases. Americans spend another $330 billion each year for hospitalization, home health care, medication, and lost productivity associated with cardiovascular diseases.

Suppose that, over the next decade, it turns out that the 2020-21 lockdown saved a total of 1.1 million US lives (including people who may have contracted Covid in 2020-21 but died over the subsequent decade from lingering complications). This is three times the 370,000 the lockdown appears to have saved in 2020 alone. We will have spent $16 trillion in direct costs and lost productivity to save those 1.1 million people. But, over the same decade, 6.6 million people will have died of cardiovascular diseases. To save them, we will have spent $3.3 trillion. We are dedicating one-fifth the resources to fighting a disease that kills six times the number of people. That makes no sense.

Of course, Covid and cardiovascular diseases are very different in that heart disease isn’t contagious. And yet, that criticism cuts both ways: because heart disease isn’t contagious, we can’t develop a herd immunity, and so heart disease will remain with us for generations whereas Covid will not.

None of this is to say that we shouldn’t have taken measures to halt Covid’s spread. It is to say that there is something markedly broken about a public policy response that spends five times the resources on a threat that is one-sixth as deadly as the single most deadly thing that kills Americans.

We got here because politicians’ survival incentive is to do whatever it takes to secure our votes, and the media’s profit incentive is to say whatever it takes to bring us back looking for more. As Omicron looms, and as surely as Pi, Rho, and Sigma will follow, voters should meet their fears with reason, view the media with a skeptical eye, and demand that politicians discuss tradeoffs openly and honestly.
 

marsh

On TB every waking moment
View: https://www.youtube.com/watch?v=GMMTw0MAT-8
22:05 min

Pfizer COVID 19 FDA Authorized Pill "Paxlovid" Explained

Dec 29, 2021


MedCram - Medical Lectures Explained CLEARLY


Roger Seheult, MD of MedCram illustrates how the Pfizer coronavirus pill called Paxlovid works, its efficacy, and its side effects. See all Dr. Seheult's videos at: https://www.medcram.com Clinical trial data for Paxlovid show that if taken within 3 days of symptom onset, hospitalizations and death were reduced by 89% compared to placebo. (This video was recorded on December 29, 2021) Roger Seheult, MD is the co-founder and lead professor at https://www.medcram.com He is Board Certified in Internal Medicine, Pulmonary Disease, Critical Care, and Sleep Medicine and an Associate Professor at the University of California, Riverside School of Medicine.

LINKS / REFERENCES: Pfizer Announces Additional Phase 2/3 Study Results (Pfizer) | https://www.pfizer.com/news/press-rel... Pfizer’s Novel COVID-19 Oral Antiviral Treatment Candidate (Pfizer) | https://www.pfizer.com/news/press-rel... How Pfizer's New Drug Fights COVID [PAXLOVID] (Simplifying Synthesis) | https://youtu.be/HHzaiAwJpfQ The SARS-CoV-2 main protease as drug target (PMC) | https://www.ncbi.nlm.nih.gov/pmc/arti... Covid-19: Pfizer’s antiviral Paxlovid effective against severe disease and Omicron variant (Pharmaceutical Technology) | https://www.pharmaceutical-technology...
 

marsh

On TB every waking moment

Secret Agreement Formed by US Government to Own 'Vaccine' During COVID-19's First Origins
"There you have it. The U.S. government has a documented, verifiable conflict-of-interest in issuing federal vaccine mandates."
Kyle Becker
Dec 11
The U.S. government entered into a secretive agreement with one of the major mRNA 'vaccine' manufacturers, Moderna, right as China began mobilizing in preparation for the forthcoming coronavirus pandemic.

The NIH-and-Moderna confidential agreement was formed only months prior to the COVID-19 pandemic sweeping the world in late October and December 2019. However, May 2019 would be a pivotal period in the genesis of the coronavirus in China, as this report will highlight below.

"In May 2019, NIH and Moderna entered into a 'research collaboration agreement' to develop vaccine candidates against Middle East Respiratory Syndrome coronavirus (MERS-CoV) and Nipah virus," a Public Citizen investigation notes. "The project was focused on evaluating candidates in animal models. NIH signed an amendment to the document on January 13, 2020—the day the agency and Moderna finalized the design of their novel coronavirus vaccine. The amendment is significantly redacted and does not mention the new coronavirus. However, the close proximity suggests the terms of the contract may have been expanded to apply to this new project. At the very least, the terms may have been instructive for the mRNA-1273 project."

The NIH-Moderna secret agreement was in close proximity to another event: China's initial mobilizations for a coming coronavirus pandemic in May 2019.

"Purchases of PCR tests in China's Hubei Province surged months before the first official reports of a novel coronavirus case there, according to a report by Australia-based cybersecurity company Internet 2.0," Nikkei Asia reported.

"About 67.4 million yuan ($10.5 million at current rates) was spent on PCR tests in Hubei during 2019, nearly double the 2018 total, with the upswing starting in May, according to the report."

"The report casts further doubt on China's official line about the origins of the virus, a topic that has fueled tensions between Beijing and Washington," Nikkei Asia added. "China's foreign ministry has disputed the report's findings."

However, the NIH and Moderna had been working together for at least four years on an mRNA drug for coronaviruses. It was only in May 2019 that the confidential agreement was entered into.

(The rest of the article is behind a paywall)

Also, ref Glen Beck Nov. special, which included the US/Moderna contract:
View: https://youtu.be/91Ib5NjSZ-o
2:01:10 min
 
Last edited:

marsh

On TB every waking moment

Shell Game? There remains no FDA approved COVID vaccine in the United States

Is Pfizer is using children as legal human shields to get full authorization?

I fact checked the fact checkers and couldn’t believe what I found. Despite the corporate press, Big Pharma, and the federal government telling us otherwise, it is absolutely true that there is no FDA approved COVID-19 vaccine available in the United States today. And there are no plans to make one available any time soon.

I know it’s hard to believe, but it’s 100% true. And this reality hints at an incredible scandal within both Big Pharma and the U.S. Public Health bureaucracy.

On August 23, the FDA granted full approval for a COVID-19 vaccine to Pfizer-BioNtech for a specific product sold under the brand name Comirnaty. The landmark moment — the “full approval” endorsement from the FDA — was heralded by the Biden Administration and countless states, and quickly leveraged to coerce millions into taking the shots. This product, Comirnaty, was fully authorized for the “prevention of COVID-19 disease in individuals 16 years of age and older.”

Yet Comirnaty itself has never made its way into the United States. The fully-approved version is nowhere to be found within our borders.

A separate product, which remains under emergency use authorization (EUA), is the only “Pfizer shot” available in the United States.

Early on, Pfizer and its government allies seemed to have a reasonable explanation for this issue. They claimed that Comirnaty was not yet available because the EUA shots were still lining the shelves, and claimed that the FDA-approved version would be available to all soon.

Now, it’s been over 4 months since full approval, and Comirnaty is still not being distributed.

The FDA has recognized Comirnaty as a “legally distinct” product with “certain differences,” but claims it does not impact safety or effectiveness of the shots.

“Fact checkers” leverage the latter point of safety and efficacy to claim that people are still getting access to ingredients akin to the fully approved product.
But here’s the issue: they have yet to explain why people still can’t get Comirnaty, now 128 days after full approval.

And if it is the case that the two products are the exact same thing, the FDA has not explained why they only approved a distinct product named Comirnaty, and not the injection currently being sold under the EUA label. Why won’t the FDA approve the EUA product?

FDA website
The CDC continues to confirm that Comirnaty is “not orderable at this time.” Moreover, the CDC currently states that “Pfizer does not plan to produce any product with these NDCs (National Drug Codes) and labels over the next few months while EUA authorized product is still available and being made available for U.S. distribution.”

CDC website
Now, back to the trillion dollar EUA question.

Is Pfizer refusing to make the fully authorized version available, while continuing to sell an EUA product because doing so could open up Pfizer and BioNTech to legal liability issues?

Pfizer and an HHS spokesperson talked to The Washington Post in a previous “fact check,” and claimed that there’s no additional legal immunity benefits between the EUA product and Comirnaty. However, these entities have never explained why Pfizer and the federal government would go through the trouble of recognizing two legally distinct products.

An EUA fully protects the drugmaker and grants zero legal recourse to the patient. This surefire protection measure was bolstered by the PREP act and other measures implemented to shield COVID companies from liability.


Now, here’s where it all gets very nefarious.

Due to a law passed during the Reagan Administration, in order for drug makers to be granted more robust legal liability protection for their vaccines, they must first secure full approval for the children’s version of their shot. Steve Kirsch has explained this at length last month on his Substack. Additionally, Robert Kennedy Jr mentioned it on a recent podcast with Mikhaila Peterson. I looked into these claims extensively, and they appear accurate. The National Childhood Vaccine Injury Act (NCVIA), which was passed into law in 1986, provides a legal liability shield to drug manufacturers if they receive full authorization for all ages.

Is Pfizer seeking approval for children so that it can protect itself from lawsuits? The company is working with regulators, even clandestinely altering vaccine ingredients (a process that should require them to get full approval for an entirely separate product), in a seeming bid to clear the path to legal indemnity.

Twitter avatar for @JeanRees10 Jean Rees @JeanRees10
Pfizer has been enabled to change formulations on no publicly available data New - "Gray Cap" 12+ vax w/Tris (never trialed in any age for the Pfizer ) Public 5-11 yos are 1st to receive Tris formulation, clinical trial was PBS. FDA memo unclear on Comirnaty or BNT162b2

Image

Image
December 29th 2021



Surely, there’s also a monetary incentive in play, but maybe there’s another reason why Pfizer, Moderna, and others are working relentlessly to authorize their products for children, who face near-zero risk from COVID-19, but continue to showcase alarming side effects from the vaccine. A vaccine on the children’s schedule provides a definitive, government-incentivized liability boost.

Twitter avatar for @TheChiefNerd Chief Nerd @TheChiefNerd
New Hong Kong study finds a 1-in-3000 adolescents developed myocarditis following vaccination “There is a significant increase in the risk of acute myocarditis/pericarditis following Comirnaty vaccination among Chinese male adolescents, especially after the second dose.”

Image
December 27th 2021




Twitter avatar for @trencherman333 Steve Ross @trencherman333
@SueWagnerWhite @CisPeoplekind @JerelKuehn @mmk_blahblah once-healthy 12 yr old Maddy de Garay from Ohio was volunteered by her family for Pfizer trial After 2 doses she is now paralyzed from the waist down, in a wheelchair, has seizures & memory loss Her remorse-filled Mom said " we just wanted to show we believed in The Science..."

Image
October 16th 2021


If Comirnaty becomes available for all ages, that means Pfizer receives an extensive, additional layer of protection.

Is Big Pharma using children as legal human shields for their products?

There is currently no fully authorized COVID-19 vaccine available in the United States today, and this reality has been attacked relentlessly by the corporate press. "Fact checkers" at Newsweek, USA Today, Reuters the Associated Press, and elsewhere peddled false information to cover up this absolute fact.

If you run a Google search on this issue, you will find the aforementioned “fact checks” as evidence that Comirnaty is available, when it is most certainly not available. Nobody in the United States is receiving the legally distinct, fully authorized shot. Is it because that shot makes Big Pharma and corrupt regulators more legally vulnerable than they want to be?

[This piece has been updated to reflect that both Pfizer and the federal government claim that Comirnaty has the same legal protections as the EUA product.

However, there remains no compelling explanation for why there are two distinct products, and why one is being delivered under EUA, and the fully authorized version is not available
.]
 

marsh

On TB every waking moment

CDC Director Walensky Says Updated Covid Guidance Based on What Agency “Thought People Would be Able to Tolerate” (VIDEO)

By Cristina Laila
Published December 29, 2021 at 8:34pm
IMG_8671.jpg

And here it is.

CDC Director Rochelle Walensky on Wednesday said the agency’s updated Covid guidance was based on [as much tyranny] as people would tolerate.

The CDC suddenly updated its Covid guidelines and took into consideration the economic impact that long quarantine times and forced isolation has on society.

A quick recap of the CDC’s sudden shift in the last 48 hours after Biden said “there is no federal solution to Covid”:
  • The CDC was wrong about Omicron and they suddenly shifted their guidelines on quarantine times in just a matter of 24 hours.
  • The CDC on Monday recommended shorter Covid isolation and quarantine time for all Americans.
  • The CDC made the decision to cut isolation time from 10 to 5 days in an effort to help Joe Biden and make sure there isn’t a total collapse of society under his watch.
  • The CDC withdrew the use of PCR tests for Covid and finally admitted the test cannot differentiate between Covid and the flu.
  • The CDC also admitted testing at the end of isolation is no longer needed because the PCR and antigen tests are faulty.
CDC Director Walensky on Wednesday said the decision to update Covid guidelines was in part due to making sure society doesn’t collapse.

Then she said this…

“It really had a lot to do with what we thought people would be able to tolerate,” Walensky said.

VIDEO:

View: https://twitter.com/i/status/1476181419063971840
.43 min
 

marsh

On TB every waking moment

FAA Dangerously Ignores Its Own Guidelines – Clears Vaccinated Pilots to Fly Despite “Do Not Issue—Do Not Fly” Policy

By Julian Conradson
Published December 29, 2021 at 9:05pm
plane-ukraine.jpg


The Federal Aviation Administration (FAA) has been exposed for flagrantly violating its own safety guidelines in order to push the experimental Covid-19 vaccine.

According to the FAA’s own policy, pilots should not fly after having taken medications that have been approved for less than a year, but the agency has systematically ignored those rulesclearing pilots to fly after waiting just two days from their date of vaccination, without knowing the full scope of the long-term effects of these vaccines.

From the FAA rules:
For any medication, the AME (Aviation Medical Examiner) should ascertain for what condition the medication is being used, how long, frequency, and any side effects of the medication. The safety impact of the underlying condition should also be considered.

Do Not Issue. AMEs should not issue airmen medical certificates to applicants who are using these classes of medications or medications.
  • FDA (Food and Drug Administration) approved less than 12 months ago. The FAA generally requires at least one year of post-marketing experience with a new drug before consideration for aeromedical certification purposes.
This observation period allows time for uncommon, but aeromedically significant, adverse effects to manifest themselves.
On top of that, the Covid vaccines in question are NOT fully approved by the FDA. Instead, they are still being issued under the agency’s Emergency Use Authorization (EUA) because the vaccine (Comirnaty) that was granted full approval is not being administered in the US as of now.

In other words, these pilots who take the rushed EUA vaccine would traditionally lose their ability to fly, but the FAA is clearing them anyway – after just two days.

From the FAA website:
The Federal Air Surgeon determined that FAA medical certificate holders may not act as pilot in command, or in any other capacity as a required flightcrew member, for 48 hours after each dose of the Pfizer-BioNTech, Moderna, and Johnson & Johnson vaccines.
The Federal Air Surgeon made this determination after evaluation of available medical information about these COVID-19 vaccines and potential side effects.”
Earlier this week, a group of independent attorneys, doctors, and other experts sounded the alarm over the agency’s violations when they submitted a letter to the FAA, the Department of Transportation, The Department of Justice, and the leaders of several large airlines, demanding that officials immediately flag all vaccinated pilots and have them re-examined for known, potential side-effects of the vaccine, such as blood clotting and other cardiac issues.

From their letter, titled “The Federal Aviation Administration is putting both Pilots AND the General Public at Risk by Forcing Vaccine Mandates!”:
“Notice to FAA That Pilots Are Operating Commercial Aircraft in Contravention of Do-Not-Fly Regulations -Title 14 Code of Federal Regulations §61.53 (also known as Federal Aviation Regulation 61.53) and Associated Guidance – Which Disallow Medical Clearance of Pilots Who Have Injected Non- FDA Approved Medical Products, such as COVID-19 Vaccinations
Pilots Flying with Abnormal Troponin Values and/or New ECG Changes/Cardiac MRI Changes – Which Indicate Active Heart Damage and Possible Acute Myocarditis – Are at Elevated Risk for Arrhythmias, Cardiac Arrest, and Death While In-Flight;
Notice to the FAA, All Commercial Airline Companies, and All Carriers Insuring Commercial Airlines That a Failure to Immediately Investigate this Issue, Correctly Apply Federal Do-Not-Fly Regulations – and Ground All Vaccinated Pilots Who Cannot Show Clean D-Dimer, Troponin, ECG and Cardiac MRI TestsCould Lead to a Catastrophic Event Involving Mass Fatalities, Causing At-Fault Parties to Suffer Monetary Liability Potentially Extending to USD Hundreds of Millions.”
Human rights attorney and primary author of the letter, Leigh Dundas, explained the group’s concerns via email to The Epoch Times. She points out that the title of the section in the FAA’s own guidelines “literally says Do Not Issue—Do Not Fly” in regards to pilots being cleared for duty. The guidelines even clearly instruct medical examiners to “not issue” medical certifications to pilots who use medical products, including vaccines, that were recently approved, or not approved, by the FDA.

According to Dundas, who spoke with The Epoch Times via email, the FAA’s negligence could lead to a catastrophe if one of these pilots experiences a vaccine-related adverse reaction while in-flight.
“The Federal Aviation Agency is charged with ensuring the safety of the flying public. Instead, as we speak the FAA, as well as the commercial airline companies, are acting in contravention of their own federal aviation regulations and associated guidance which tells medical examiners to NOT issue medical certifications to pilots using non-FDA approved products.
“The title of the section I’m talking about literally says ‘Do Not Issue—Do Not Fly’ and then instructs medical examiners to ‘not issue’ medical certifications to pilots using products that the FDA ‘approved less than 12 months ago.’
The pilots are flying with products which are not even recently approved—in violation of the above wording—they are flying with injections in their bodies which were NEVER approved by the FDA at all (as no COVID vaccine which is commercially available in the U.S. has received FDA approval).”
Another one of the letter’s signees is Cody Flint, whose career as a pilot recently came to an end after he experienced adverse reactions to the vaccine while he was mid-air, piloting a flight.

The 34-year-old agricultural pilot doesn’t even remember how he landed after nearly blacking out in mid-flight, but thankfully he ended up safely on the ground.

From Epoch Times:
He [Flint] was flying his aircraft when tunnel vision started to kick in and a headache he had developed after getting the jab worsened.
About two hours after having taken off, he decided to pull up the plane to go back and felt an ‘extreme burst of pressure” in his ears, then immediately ‘nearly blacked out, [and felt] dizzy, disoriented, nauseous, and [was] shaking uncontrollably.’
As a commercial pilot, Flint was concerned when he first saw FAA’s 48-hour no-fly rule after a COVID-19 vaccination.
I find it hard to comprehend how the FAA justified moving the goalposts of safety from one full year of post-marketing safety review to only two days. The dangers associated with a pilot experiencing a severe adverse reaction from an mRNA-type Covid vaccine while at the controls of an airplane can be horrifying and deadly to say the least.
‘As a pilot that experienced a tragic and career-ending adverse reaction to the Pfizer COVID vaccine while actively flying an airplane, I feel I can honestly and creditably speak out about the dangers associated with pilots returning to flight duties too early following COVID mRNA type vaccination,” he added.”
In addition to Flint and Dundas, several other notable experts signed on to the letter, including Aerospace Occupational Medicine Specialist LTC Colonel Theresa Long, Robert F. Kennedy Jr., Dr. Peter McCullough, Dr. Ryan Cole, and Mary Holland from Children’s Health Defense.

Hopefully, their warning is heeded before a tragedy happens that could have been prevented. At the very least the FAA should be regularly screening the health of these pilots for an extended period of time after they have received a dose of the vaccine. Anything less seems almost criminal, especially considering the seriousness of the known adverse events tied to these mRNA vaccines.
 

marsh

On TB every waking moment

Pandemic of the Vaccinated: Two Studies Show New Evidence that Covid-19 Vaccines “Cause More Illness than They Prevent”

By Julian Conradson
Published December 29, 2021 at 7:57pm
Screen-Shot-2021-12-22-at-3.50.58-PM-913x479.jpg


Pandemic of the Vaccinated: Two Studies Show New Evidence that Covid-19 Vaccines “Cause MORE ILLNESS than they Prevent” – After 3 Months, Pfizer Jab Recipients are 76.5% MORE LIKELY than the Unvaxxed to Contract Covid
Two newly released studies show that – after a brief period of moderate protection – the experimental Covid-19 vaccines actually end up causing more illness than they prevent – especially when it comes to new variants like the now-predominant, and highly-mild Omicron.

The first study, a pre-print that was released on MedRXiv by a team of researchers in Denmark, shows that the experimental vaccines provide absolutely zero protection against Omicron beginning two months after vaccination (which they refer to as “peak” protection).

After just three months, fully vaccinated individuals begin to experience sharp negative protection. Researchers found that those who received the Pfizer vaccine were an astounding 76.5% more likely to have a breakthrough infection than their unvaccinated counterparts once 90 days had passedthose who received Moderna’s were 39.3% more likely.

According to the study, the spread of the new Omicron variant was “likely” caused by “super-spreader events” “among young, vaccinated individuals.”

Only those who had taken a complete two-dose vaccination or a two-dose vaccination and a booster were counted as vaccinated in the study.

Somehow, the study’s authors still conclude that mass vaccination and the rollout of boosters is nessecary.

Take your booster, sheep.

Look:
Screenshot_20211229-184729_Chrome-913x479.jpg


1640838207586.png

As if that wasn’t enough proof that this is the ‘pandemic of the vaccinated,’ the Canadian Covid Care Alliance – a non-profit government watchdog group of independent health care professionals – released a separate report this week that came to similar conclusions.

After examining Pfizer’s own vaccine clinical trial data, the CCCA team of experts also found that the Pfizer vaccine had serious negative protection against Covid, and so much so that they concluded the “vaccine causes more harm than good.”
“The Pfizer 6 month data shows that Pfizer’s COVID-19 inoculations cause more illness than they prevent.“
The CCCA panel conducted a thorough analysis of Pfizer’s vaccine trial report from December 31st, 2020. The Pfizer report claims that the inoculations were safe and showed a robust 95% efficacy 7 days after the 2nd dose. But what researchers failed to mention was that the 95% was actually Relative Risk Reduction. Absolute Risk Reduction, which is what should have been factored in – especially if this vaccine is going to be mandated across the board, was less than one percent.
“The claim was that the inoculations were safe and showed 95% efficacy 7 days after the 2nd dose. But that 95% was actually Relative Risk Reduction. Absolute Risk Reduction was only 0.84%.”
For context, relative risk reductions only relate to a percentage reduction in one group compared to another, which can easily be misleading and over-exaggerate how helpful something is. Absolute risk reductions give the actual difference in risk between one group and another.

The report also shows that Pfizer had recorded an increased risk of illness – and even an increased risk of death – in individuals who had taken the vaccine compared to those who were in the placebo group – something that was also backed up by Pfizer’s latest clinical trial data that was published last month.

From CCCA:
“Pfizer’s most recent report indicates an Efficacy of 91.3%. (Which means a reduction in positive cases compared to placebo group.)

But it also showed, compared to the placebo group, an increase in illness and deaths.

There is no benefit to a reduction in cases if it comes at the cost of increased sickness and death.”
“Severe adverse events” were up by 75% in the trial group that had received the vaccine.

Overall, adverse events that were attributed to the vaccine
were an astounding 300% higher than in the placebo group.

Screenshot_20211229-173834_Samsung-Notes-913x479.jpg


As for deaths, there were more who died in the vaccinated group 20 out of 34 total. What’s even more concerning is that 9 of the vaccinated deaths were related to “cardiovascular events.

Screenshot_20211229-173850_Samsung-Notes-913x479.jpg


The CCCA panel also found several questionable and corrupt practices that were used when Pfizer compiled their report.

Not only did the vaccine maker downplay the side effects of the experimental jab, but they also did not follow established clinical trial protocols, had inadequate control groups that were mixed and unblinded early, and tested the jab on misleading demographics in order to generate the best results.

Screenshot_20211229-175011_Samsung-Notes-913x479.jpg


Instead of focusing the trials on the target population who could most benefit from a Covid-19 vaccine – a la the elderly and those with severe comorbidities – Pfizer chose participants from younger demographic that would be a) less likely to need a vaccine, b) less likely to suffer an adverse event during a trial, c) more likely to respond well to a vaccine, than the elderly who need protection against this virus.

Keep in mind, children and young adults have a whopping 99.995% recovery rate from this nominal virus.

Screenshot_20211229-182146_Samsung-Notes-913x479.jpg


Additionally, because Pfizer unblinded their clinical trial groups early, they are unable to produce any relevant long-term safety data because they don’t have a control group for reference anymore.

By early 2021, nearly everyone in the study, even the placebo group had been vaccinated, which effectively ended any hope for meaningful data.

Screenshot_20211229-181201_Samsung-Notes-913x479.jpg


In what’s probably a glowing testament to its credibility, Dr. Robert Malone – the inventor of the mRNA vaccine – was permanently kicked off of Twitter for sharing the CCCA report earlier today.

If it’s getting censored, you know they are over the mark.


This is just the latest evidence that Pfizer and the public health bureaucracy fully knew the dangers of these experimental vaccines, but pushed them out to the world anyways. A few weeks back, the Gateway Pundit reported on how the FDA granted an extension to Pfizer’s EUA despite recording an astounding 1,200-plus vaccine-related deaths in just the first 90 days of its availability.

This is criminal. Where is the accountability?

 

marsh

On TB every waking moment

Lawmaker: Joe Biden Reallocated $2 Billion in COVID Testing Funds to House Illegals at the Border (VIDEO)

By Jim Hoft
Published December 29, 2021 at 5:15pm
smith-biden-illegals.jpg


Ignored by the liberal media. New Yorkers are waiting in endless lines for hours in the cold to get their test kits so they can go back to work, school or visit family because Joe Biden took the Covid relief money and sent it to house unvaccinated untested illegals at the border.

They do this because they hate you — and because New Yorkers are dupes.

Rep. Jason Smith (R-MO) broke this report earlier today on FOX News.
Rep. Jason Smith (R-MO): He reallocated $2 billion of money that should have gone towards COVID testing but instead sent it to house illegals at the border.
Wow.

Via Midnight Rider.
Rumble video .39 min
 

marsh

On TB every waking moment

1640838968471.png
fizer Inc partnered with a Chinese Communist Party payment platform which has been used to implement “vaccine passports” in China since the outbreak of COVID-19. The company said it was “proud to stand with China leaders.”

The pharmaceutical giant – whose U.S. lobbying efforts hit an all-time high in the past year – expressed its pride for the brutal, communist regime in the following tweet from June 6th, 2018:

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“We are proud to stand with China leaders & @Alipay to introduce new, digital solutions to improve disease education and vaccine access-creating a brighter future for Chinese children,” the tweet reads.

“We are honored to be a partner in China’s ‘Internet + Vaccination’ initiative,” reads an accompanying graphic, quoting Pfizer’s China General Manager Wu Kun.

The message also revealed the firm’s partnership with Alipay, a Chinese online payment platform originally founded as an offshoot of the Chinese Communist Party-linked company Alibaba.

Alibaba has also been involved in the “research, production, and repair of weapons and equipment for the People’s Liberation Army (PLA)” and has a “deep record of cooperation and collaboration” with China’s “state security bureaucracy,” according to Assistant Secretary for International Security and Nonproliferation at the U.S. State Department Christopher Ford.

The State Department has also flagged the company as a “tool” of the Chinese Communist Party, aiding in its build-up of “technology-facilitated surveillance and social control.”

Despite these ties, Pfizer partnered with the platform in 2018, as outlined in the company’s annual review:
“We’re using the Alipay platform, which has over 700 million active users in China, to provide much needed education about disease and vaccinations. Additionally, to help China reach its ambitious 2030 goals to reduce infant mortality, we are exploring the use of the platform for mobile payments to improve convenience in Chinese Point of Vaccination centers, as well as options for installment payments that may reduce the financial burden for low income families.”
The unearthing of the partnership between Alipay and Pfizer, which occurred a year prior to the onset of COVID-19, also follows China relying on the platform to institute vaccine passports. As The New York Timesexplains:
“After users fill in a form on Alipay with personal details, the software generates a QR code in one of three colors. A green code enables its holder to move about unrestricted. Someone with a yellow code may be asked to stay home for seven days. Red means a two-week quarantine.
In Hangzhou, it has become nearly impossible to get around without showing your Alipay code. Propaganda-style banners remind everyone of the rules: “Green code, travel freely. Red or yellow, report immediately.”
Alibaba was recently penalized by the CCP for failing to adhere to recent laws requiring the company to put the regime’s interests ahead of its duty to report critical cybersecurity vulnerabilities to the world.
 

marsh

On TB every waking moment

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Following his recusal from the Lancet’s COVID-19 commission, EcoHealth Alliance President Peter Daszak – a researcher whose “longtime collaboration” with the Wuhan Institute of Virology was funded by Anthony Fauci – reemerged in the mainstream media claiming the Chinese Communist Party never covered up data related to the virus.

Despite his removal from the medical journal’s commission focusing on COVID-19’s origins due to an extensive conflict of interest with the Chinese Communist Party-controlled Wuhan lab, first reported by The National Pulse, Daszak joined a BBC program, “COVID Origins: The Science.”

“Was information hidden,” the presenter asks Daszak.

Before asserting “there is no cover-up,” he explains:
Not from me. I mean, we…. Not from the public, actually. I mean, you hear this thing so often that you begin to sort of believe it.
The claim follows nearly 20,000 bat coronavirus samples getting erased from the Wuhan Institute of Virology in late 2019 and the lab continuing to do so throughout the pandemic. The National Pulse has also documented how the lab deleted mentions of its manipulation of bat coronaviruses to become more lethal, its partnership with the U.S. National Institutes of Health, names of military researchers working at the lab, and articles documenting its financial and personnel ties o the Chinese Communist Party from its website.

The lab has also erased reports of its researchers getting bitten by wild bats.

Daszak, who also served on the World Health Organization (WHO) COVID-19 origins investigation team, also revealed that the delegation never visited the farms believed to be the source of the animal carrying the virus crucial to the “wet market theory”:
We knew we weren’t going to go out and do testing of animals. You know, you’ve got a month in China, two weeks on the ground. You know, you’re in lockdown for two weeks. We knew we weren’t going to be able to travel to the wildlife farms and sample animals and get them tested.
The BBC program also describes the type of controversial research – “gain-of-function” – likely conducted by EcoHealth Alliance and the Wuhan Institute of Virology despite Fauci’s repeated insistence otherwise:
The researchers were also working their way through their samples to see whether any of the coronaviruses they did find on their searches presented a danger to humans. Live virus was unlikely to be found, but genetic material was, and one method of checking was to make spike protein from these new samples, graft it onto known viruses like WIV1, and see whether the engineered virus would then infect human cells or infect mice engineered to carry this human ACE2 receptor. When you hear of gain-of-function experiments, this is what they’re likely talking about. Although, the description is disputed.
 

vestige

Deceased

View attachment 310336

Following his recusal from the Lancet’s COVID-19 commission, EcoHealth Alliance President Peter Daszak – a researcher whose “longtime collaboration” with the Wuhan Institute of Virology was funded by Anthony Fauci – reemerged in the mainstream media claiming the Chinese Communist Party never covered up data related to the virus.

Despite his removal from the medical journal’s commission focusing on COVID-19’s origins due to an extensive conflict of interest with the Chinese Communist Party-controlled Wuhan lab, first reported by The National Pulse, Daszak joined a BBC program, “COVID Origins: The Science.”

“Was information hidden,” the presenter asks Daszak.

Before asserting “there is no cover-up,” he explains:

The claim follows nearly 20,000 bat coronavirus samples getting erased from the Wuhan Institute of Virology in late 2019 and the lab continuing to do so throughout the pandemic. The National Pulse has also documented how the lab deleted mentions of its manipulation of bat coronaviruses to become more lethal, its partnership with the U.S. National Institutes of Health, names of military researchers working at the lab, and articles documenting its financial and personnel ties o the Chinese Communist Party from its website.

The lab has also erased reports of its researchers getting bitten by wild bats.

Daszak, who also served on the World Health Organization (WHO) COVID-19 origins investigation team, also revealed that the delegation never visited the farms believed to be the source of the animal carrying the virus crucial to the “wet market theory”:

The BBC program also describes the type of controversial research – “gain-of-function” – likely conducted by EcoHealth Alliance and the Wuhan Institute of Virology despite Fauci’s repeated insistence otherwise:
F*** China

F*** Fauci

Top that
 

marsh

On TB every waking moment

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Simulations conducted by Oracle supercomputing revealed COVID-19 to be “highly adapted” for human infection, discrediting the claim of the virus counting natural origins through a spillover event from wildlife to humans.

As revealed in Sharri Markson’s What Really Happened In Wuhan, Flinders University Professor and Research Director at Vaxine Dr. Nikolai Petrovsky used an Oracle supercomputer’s “in silico modeling” approach to identify COVID-19’s original host.

Proponents of the “natural origins” theory – including many Chinese Communist Party-compromised scientists – have attached significance to the virus’s host being a bat, arguing the animal transferred COVID-19 to a person at a wet market.

Petrovsky’s findings, which appear to identify humans as the original host of COVID-19, undercut the theory that the virus was transferred from animal to human but rather originated in humans independent of an animal.

To do so, Petrovsky’s team analyzed different ACE2 receptors, which allow coronaviruses to enter cells and reproduce, and spike proteins, which allow the virus to actually latch onto a human’s airway cells with the supercomputer.

“We were trying to find which species of lock the Covid-19 key was best designed to unlock. You can try and fit the SARS-CoV-2 spike protein structure shape into all of the ACE2 structures from different animals to see which one fits best, just like solving a jigsaw,” Petrovsky explained.

The group uploaded ACE2 genetic sequences from a variety of potential animal hosts including bats, mice, and civets and was able to run simulations by March 2020. As What Really Happened In Wuhan notes:
Very quickly, he had a result – and it was a result that caused him a great deal of angst. “Strangely, humans came out at the very top of the list.” Petrovsky pauses. “That was not what we were expecting, as the animal host from which the virus had been transmitted should have been at the top of the list. This presented a puzzle as the data suggested the SARS-CoV-2 spike protein had uniquely evolved to bind and infect cells expressing human ACE2. Normally with a new pandemic virus, whatever species that virus originally came from would be the best fit and the virus would initially only half fit the human lock but then mutate over time to try and become a better fit. A virus should not be able to evolve to be a perfect fit for a lock it has never seen, and yet this is what the data was telling us. The virus spike protein looked like it couldn’t have been better designed to fit the human ACE2. Go figure.”
Eventually, Petrovsky’s team published its findings in June 2021 in the prestigious journal, Nature Scientific Reports, in a report titled “In silico comparison of spike protein-ACE2 binding affinities across species; significance for the possible origin of the SARS-CoV-2 virus.”

“Notably, SARS-CoV-2 spike protein had the highest overall binding energy for human ACE2, greater than all the other tested species including bat, the postulated source of the virus. This indicates that SARS-CoV-2 is a highly adapted human pathogen,” noted the paper.

“This finding is particularly surprising as, typically, a virus, would be expected to have highest affinity for the receptor in its original host species, e.g. bat, with a lower initial binding affinity for the receptor of any new host, e.g. humans,” it continued.
 

marsh

On TB every waking moment

Biden's CDC director says she is considering allowing booster shots for 12-year-olds

In an interview with CNN, Walensky said that "the first thing to note is to get your children vaccinated."
Biden's CDC director says she is considering allowing booster shots for 12-year-olds


The Post MillennialThe Post Millennial

December 29, 2021 9:22 PM1 Mins Reading

President Joe Biden's appointed CDC Director Rochelle Walensky has said that the US is considering opening booster shots for 12 to 15 year olds.

In an interview with CNN, Walensky said that "the first thing to note is to get your children vaccinated."

"We have vaccine available for children above the age of five," she added. "The FDA is currently looking at the issue of booster shots for those 12 to 15 years of age."

"I know that the companies and manufactures are working towards data for under five year olds. That will not be in the months ahead, but we're working to get there soon."

The CDC director then said that she understood that parents want a booster shot for their children with rising number of cases, deriving from the omicron variant.

She said the CDC would look to follow with this as soon as they receive more information from the vaccine manufacturers.

On Monday, Walensky cut quarantine restrictions for Americans who contract COVID-19 down from 10 days to five days. Similarly, the CDC has also shortened the time that close contacts are required to quarantine.

CDC officials stated that the guidance is based on growing evidence that people who catch the coronavirus are most infectious in the two days before and three days after symptoms develop, The Associated Press reported.
 

marsh

On TB every waking moment

Beware Pfizer’s New Drug Paxlovid

by Dr. Joel S. Hirschhorn
December 29, 2021
Beware Pfizer's New Drug Paxlovid


The pro-drug industry mainstream media are insanely positive over the newly FDA-approved Pfizer antiviral COVID treatment pills. The drug, Paxlovid, received an emergency use authorization by FDA for use in patients 12 years old and up who have tested positive for COVID-19 and are at high risk.

Now is the time to speak truth about Paxlovid. First, everyone should appreciate that there was very little testing of the short- and long-term safety of this product, exactly what happened with COVID vaccines. Really good testing of a new drug should take many months or even years.
Does the public really want to take an HIV/AIDS drug?
All you get is positive news for this new drug – actually a combination of drugs.

Here are brief summary statements about this new product:

It was approved by the FDA without any external meetings, serious reviews of test data or opportunity for public input. Pretty much all the regulatory work was done behind closed doors. Terrific for Pfizer. Bad for the public.

Of importance, note that in the trials only 21% of people had a comorbidity, while in reality 94% of COVID deaths have at least one comorbidity, and the average number of underlying medical conditions is four.

As to antiviral science, protease enzymes must be present for the virus to successfully infect by completing the cycle before taking the cell over. Paxlovid or any drug classified as a ‘Protease Inhibitor’ will inhibit or decrease the protease enzyme interfering with the virus. Paxlovid blocks the 3CLPro protease from chopping up the long protein into pieces. The virus can’t separate out which pieces to cut out and assemble. It can’t make copies of itself. The covid infection quickly stops.
How interesting it would have been to test the Pfizer drug against an ivermectin protocol.
Contrary to what the government says, ivermectin is the most successful and proven protease inhibitor in use worldwide. Just as with Paxlovid, ivermectin decreases the protease enzyme but there are benefits of ivermectin in covid treatment that are not present in Paxlovid. Additional actions of ivermectin include anti-coagulant action and anti-inflammatory actions, both observed in covid infections. Moreover, ivermectin has been safely used for decades and there have been many medical studies as well as clinical results showing its antiviral and anti-inflammatory effectiveness.

Paxlovid requires combination with an HIV/AIDS drug, Ritonavir, preventing the breakdown of the Paxlovid so it may inhibit or decrease the enzyme interrupting the viral life cycle. Ritonavir acts as a booster for Paxlovid, keeping it active inside a person’s body. Ritonavir also has its own black box warning and side effects include life-threatening liver, pancreas and heart issues. Does the public really want to take an HIV/AIDS drug?

A course of the treatment is 20 Paxlovid pills and 10 ritonavir pills taken over five days. Taking 6 pills daily can pose challenges for many elderly people in particular.

According to Pfizer’s press release, for people with proven COVID infection, Paxlovid reduces hospitalization/death by 89% when taken within three days of symptom onset. So in the treatment group there was 5 of 697 hospitalized with no deaths compared to 44/682 hospitalized with 9 subsequent deaths.

Think about that statement of taking this drug combo within three days of symptom onset. Here are critical problems facing ordinary people:
  • How can you accurately identify COVID symptoms from similar symptoms with the flu or a bad cold?
  • How can you get in touch with your doctor within just a day or two and decide whether you really have COVID and if so get a prescription?
  • How can you get the prescription filled quickly?
None of these are easy to address and overcome. All this makes this new combo medicine unrealistic and impractical for nearly everyone.

Also reported was an approximate 10-fold decrease in viral load at day 5, relative to placebo, indicating robust activity against SARS-CoV-2 and representing (supposedly) the strongest viral load reduction reported to date for a COVID-19 oral antiviral agent.

How interesting it would have been to test the Pfizer drug against an ivermectin protocol.

For example, how does the Pfizer drug compare with the Dr. George Fareed and Dr. Brian Tyson protocol? Well, Fareed and Tyson had many more patients (about 7,000) taking the drug combo and yet they had fewer hospitalizations (4) and the same number of deaths (0). So, you’re way better off with the Fareed and Tyson protocol. And the safety protocol of IVM after billions of uses globally is far better proven than for the Pfizer product.

For a good discussion on how IVM compares to Paxlovid see this article, especially on scientific evidence of ivermectin’s ability to block 3CL protease.

In terms of safety, the most common side effects reported during treatment and up to 34 days after the last dose of Paxlovid were dysgeusia (taste disturbance), diarrhea and vomiting. But what more serious side effects may turn up months or years later?

Paxlovid must not be used with certain other medicines, either due to its action that may lead to harmful increases in their blood levels, or because some medicines may reduce the activity of Paxlovid itself. The list of medicines that must not be used with Paxlovid is included in the proposed conditions for use. That list includes a very large number of drugs and supplements used by many millions of people, including, for example, Lipitor and St. John’s Wort. Paxlovid must also not be used in patients with severely reduced kidney or liver function.
Always follow the money.
Paxlovid is not recommended during pregnancy and in people who can become pregnant and who are not using contraception. Breastfeeding should be interrupted during treatment. These recommendations are because laboratory studies in animals suggest that high doses of Paxlovid may impact the growth of the fetus.

As to availability, Pfizer CEO Bourla recently said the company can manufacture 80 million courses in 2022, with 30 million available in the first half of the year.

That is not enough to serve many millions of Americans coming down with symptoms and a positive test result.

This too was said, tens of thousands of the pills will ship in the US before the end of 2021 and hundreds of thousands more are expected at the beginning of 2022, a Pfizer spokesperson told the Wall Street Journal. The US government is paying Pfizer $5.3 billion for 10 million treatment courses that will be delivered by the end of next year, according to the paper. Will medical insurance cover $530 per course?

Always follow the money. A month ago, SVB Leerink analyst Geoffrey Porges projected the drug will generate $24.2 billion in 2022 sales. Together with the company’s megablockbuster COVID-19 vaccine, Pfizer could be looking at $50 billion in peak pandemic vaccine and drug sales, Cantor Fitzgerald analyst Louise Chen wrote earlier this month. It’s no surprise that some top Pfizer executives have become billionaires.
 

marsh

On TB every waking moment

New York Times: COVID Boosters May Cause 'Immune System Fatigue,' Compromise Ability to Fight Virus

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By Andrew White December 28, 2021 at 3:27pm

The New York Times reported that experts advised caution before Israel approved a fourth COVID-19 vaccine injection, warning that too many shots might actually harm the body’s ability to fight the virus by causing “immune system fatigue.”

As Israel rolls out a fourth COVID-19 vaccine injection to curb the spread of the Omicron variant, experts are now warning that too many injections may cause “immune system fatigue,” and actually compromise the body’s ability to fight the virus, the New York Times reported.

From the report:
“JERUSALEM — Israel is considering whether to approve a fourth Covid-19 vaccine dose for vulnerable people to contain the fast-spreading Omicron variant, despite debate among scientists and a lack of evidence either for or against another booster.

The panel of experts advising the Israeli government on the pandemic recognized that uncertainty, but on Tuesday it recommended giving a fourth dose, concluding that the potential benefits outweighed the risks. It pointed to signs of waning immunity a few months after the third shot, and said that any delay in additional doses might prove too late to protect those most at risk.

But some scientists warned that the plan could backfire, because too many shots might cause a sort of immune system fatigue, compromising the body’s ability to fight the coronavirus. A few members of the government’s advisory panel raised that concern with respect to the elderly, according to a written summary of the discussion obtained by The New York Times.”
Prime Minister Naftali Bennett has signaled his support for the fourth injection.

“The price will be higher if we don’t vaccinate,” said Dr. Boaz Lev, a member of the Israeli government advisory panel said. “We don’t have a lot of time to make decisions.”

This comes after the U.S. Center for Disease Control (CDC) found that an overwhelming majority of Omicron cases in United States were in “fully vaccinated” people, as National File previously reported.

During an interview with conservative media personality Candace Owens, President Donald Trump said his COVID-19 vaccines were one of the greatest achievements of mankind.

“The ones who get very sick and go to the hospital are the ones that don’t take the vaccine. But it’s still their choice. And if you take the vaccine, you’re protected,” he said.

“Look, the results of the vaccine are very good, and if you do get it, it’s a very minor form,” Trump continued. “People aren’t dying when they take the vaccine.”
 

marsh

On TB every waking moment

New lawsuit against Biden…
Posted by Kane on December 30, 2021 7:11 am

View: https://youtu.be/EgnHfyp0qDU
.58 min
‘Feds For Medical Freedom’ Sue Biden Over Vaccine Mandate

In response to the rigid and dictatorial federal COVID-19 vaccine mandates imposed on public servants and government contractors, the national grassroots coalition, Feds For Medical Freedom (F4MF), filed a lawsuit last week against Joe Biden and key agency members of his administration, including heads of the Departments of Transportation, Treasury, Interior, Housing and Urban Development, Defense, Veterans Affairs, Justice, Homeland Security, Energy, State, and others.

Representing over 700 Border Patrol Agents, Pilots, Diplomats, Firefighters, Contractors, and other dedicated and patriotic Americans, the lawsuit seeks preliminary and permanent injunctive relief from the Defendants “enforcing or implementing the Federal Employee Mandate and the Contractor Mandate.”

Full story from UncoverDC…
 

marsh

On TB every waking moment

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NYU Langone Health is leading the National Institute of Health’s (NIH) investigation of the long-term effects of COVID-19 (“Long COVID“). Dubbed the PASC (Post-Acute Sequelae of SARS-CoV-2 Infection) Initiative, the stated goal of the nearly $450 million project “is to rapidly improve understanding of recovery after SARS-CoV-2 infection and prevent and treat PASC.”

Supporting the study, in December 2020, Congress provided $1.15 billion in funding over four years to the NIH to subsidize research into the prolonged health outcomes of SARS-CoV-2 infection. The research will involve adult, pregnant and pediatric patients and include data on clinical information, laboratory tests, and analyses of these patients “in various stages of recovery” after COVID-19 infection. Maintaining that recovery varies significantly from patient to patient, the NIH notes significant post-acute sequelae, documenting:

“Reported symptoms among persons who have been infected with SARS-CoV-2 range from mild to incapacitating, may persist after recovery from acute disease, may involve multiple organs and systems, and can adversely affect overall quality of life. In some cases, new symptoms and findings are reported that appear linked to the timing of acute infection but emerge subsequently and evolve over time.”

NYU-NIH-Long-Covid.jpg
Screenshot / NIH.gov

NIAID-Workshop.jpg

Screenshot / NIAID Post-Acute Sequelae of COVID-19 Workshop, Dec. 3, 2020

The NIH study follows a Dec. 3, 2020 virtual workshop hosted by the National Institute of Infectious Diseases (NIAID). Indeed, research and studies into “Long COVID” have been an ongoing focus of NIH Director Francis Collins, who will retire at the end of 2021. In Feb. 2021, when announcing the new NIH initiative to study the emerging symptoms of “Long COVID,” Collins remarked:

“We do not know yet the magnitude of the problem, but given the number of individuals of all ages who have been or will be infected with SARS-CoV-2, the coronavirus that causes COVID-19, the public health impact could be profound.”

View: https://twitter.com/i/status/1473082652181807106
.45 min

In an effort to summarize what is known about patients who do not fully recover and identify key gaps in NIH knowledge about the effects of COVID-19 after infection, Collins outlined some of the underlying questions the initiative hopes to answer:
  • What does the spectrum of recovery from SARS-CoV-2 infection look like across the population?
  • How many people continue to have symptoms of COVID-19 or even develop new symptoms after acute SARS-CoV-2 infection?
  • What is the underlying biological cause of these prolonged symptoms?
  • What makes some people vulnerable to this but not others?
  • Does SARS-CoV-2 infection trigger changes in the body that increase the risk of other conditions, such as chronic heart or brain disorders?
Screenshot-2021-12-29-at-14-34-24-COVID-Vaccine-Data.png
Screenshot / Open VAERS

Designed to be “fully representative of the diversity of the U.S. population,” researchers will study Long COVID symptoms in tens of thousands of patient groups around the country. NYU—serving as the Clinical Science Core (CSC) of the study—explains that symptoms like “fatigue, shortness of breath, “brain fog,” sleep disorders, fevers, gastrointestinal symptoms, anxiety, and depression” can persist for months after recovery from the initial COVID-19 illness. As of Dec. 28, 2021, roughly 53 million Americans have tested positive for COVID-19, with nearly 800,000 deaths.

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In agreement with the NIH that “Long COVID” is around to stay, the Biden administration announced in July that “Long COVID” patients living in the U.S. are entitled to disability rights and resources under federal law, including the Americans with Disabilities Act (ADA). Pleased with Biden’s decision, two groups focused on COVID-19 chronic illness, Body Politic and Patient Led Research Collaborative, describe “Long COVID” as “one of the largest mass disabling events in modern history.”

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A newly formed central part of the NIH study is its RECOVER initiative (which stands for Researching COVID to Enhance Recovery). A central feature of RECOVER is the creation of the SARS-CoV-2 Recovery Cohort. Despite studies suggesting Long COVID is less common in children and adolescents, another critical aspect of RECOVER is the development of the “pediatric main protocol for study of Long COVID in children.”

Meanwhile, as fully vaccinated individuals are reinfected with COVID-19, reports suggest they are also not safe from developing “Long COVID.” With the design of the main study protocols complete, Stuart D. Katz, MD—director of NYU Langone’s heart failure program and principal investigator for the RECOVER CSC—underscored the urgent need of the PASC study, stating:

“The goal of the newly funded RECOVER studies, in adults, children, and in pregnant women, is to fully understand the long-term consequences of COVID-19 and the pace and extent of recovery over time. We recognize the need to urgently begin nationwide enrollment for collection of the information needed to better understand and improve treatment for long COVID-19.”
 

vestige

Deceased

View attachment 310453

NYU Langone Health is leading the National Institute of Health’s (NIH) investigation of the long-term effects of COVID-19 (“Long COVID“). Dubbed the PASC (Post-Acute Sequelae of SARS-CoV-2 Infection) Initiative, the stated goal of the nearly $450 million project “is to rapidly improve understanding of recovery after SARS-CoV-2 infection and prevent and treat PASC.”

Supporting the study, in December 2020, Congress provided $1.15 billion in funding over four years to the NIH to subsidize research into the prolonged health outcomes of SARS-CoV-2 infection. The research will involve adult, pregnant and pediatric patients and include data on clinical information, laboratory tests, and analyses of these patients “in various stages of recovery” after COVID-19 infection. Maintaining that recovery varies significantly from patient to patient, the NIH notes significant post-acute sequelae, documenting:

“Reported symptoms among persons who have been infected with SARS-CoV-2 range from mild to incapacitating, may persist after recovery from acute disease, may involve multiple organs and systems, and can adversely affect overall quality of life. In some cases, new symptoms and findings are reported that appear linked to the timing of acute infection but emerge subsequently and evolve over time.”

NYU-NIH-Long-Covid.jpg
Screenshot / NIH.gov

NIAID-Workshop.jpg

Screenshot / NIAID Post-Acute Sequelae of COVID-19 Workshop, Dec. 3, 2020

The NIH study follows a Dec. 3, 2020 virtual workshop hosted by the National Institute of Infectious Diseases (NIAID). Indeed, research and studies into “Long COVID” have been an ongoing focus of NIH Director Francis Collins, who will retire at the end of 2021. In Feb. 2021, when announcing the new NIH initiative to study the emerging symptoms of “Long COVID,” Collins remarked:

“We do not know yet the magnitude of the problem, but given the number of individuals of all ages who have been or will be infected with SARS-CoV-2, the coronavirus that causes COVID-19, the public health impact could be profound.”

View: https://twitter.com/i/status/1473082652181807106
.45 min

In an effort to summarize what is known about patients who do not fully recover and identify key gaps in NIH knowledge about the effects of COVID-19 after infection, Collins outlined some of the underlying questions the initiative hopes to answer:
  • What does the spectrum of recovery from SARS-CoV-2 infection look like across the population?
  • How many people continue to have symptoms of COVID-19 or even develop new symptoms after acute SARS-CoV-2 infection?
  • What is the underlying biological cause of these prolonged symptoms?
  • What makes some people vulnerable to this but not others?
  • Does SARS-CoV-2 infection trigger changes in the body that increase the risk of other conditions, such as chronic heart or brain disorders?
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Screenshot / Open VAERS

Designed to be “fully representative of the diversity of the U.S. population,” researchers will study Long COVID symptoms in tens of thousands of patient groups around the country. NYU—serving as the Clinical Science Core (CSC) of the study—explains that symptoms like “fatigue, shortness of breath, “brain fog,” sleep disorders, fevers, gastrointestinal symptoms, anxiety, and depression” can persist for months after recovery from the initial COVID-19 illness. As of Dec. 28, 2021, roughly 53 million Americans have tested positive for COVID-19, with nearly 800,000 deaths.

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In agreement with the NIH that “Long COVID” is around to stay, the Biden administration announced in July that “Long COVID” patients living in the U.S. are entitled to disability rights and resources under federal law, including the Americans with Disabilities Act (ADA). Pleased with Biden’s decision, two groups focused on COVID-19 chronic illness, Body Politic and Patient Led Research Collaborative, describe “Long COVID” as “one of the largest mass disabling events in modern history.”

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A newly formed central part of the NIH study is its RECOVER initiative (which stands for Researching COVID to Enhance Recovery). A central feature of RECOVER is the creation of the SARS-CoV-2 Recovery Cohort. Despite studies suggesting Long COVID is less common in children and adolescents, another critical aspect of RECOVER is the development of the “pediatric main protocol for study of Long COVID in children.”

Meanwhile, as fully vaccinated individuals are reinfected with COVID-19, reports suggest they are also not safe from developing “Long COVID.” With the design of the main study protocols complete, Stuart D. Katz, MD—director of NYU Langone’s heart failure program and principal investigator for the RECOVER CSC—underscored the urgent need of the PASC study, stating:

“The goal of the newly funded RECOVER studies, in adults, children, and in pregnant women, is to fully understand the long-term consequences of COVID-19 and the pace and extent of recovery over time. We recognize the need to urgently begin nationwide enrollment for collection of the information needed to better understand and improve treatment for long COVID-19.”
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