Francisco Goya Witches’ Sabbath 1797-98
John Campbell references the same German vit. D study I did several times, last in The End of Mass Vaxx.
Germany now has more deaths per day than 1 year ago, despite 85% of the adult population vaccinated
The Occupational Safety and Health Administration has suspended implementation and enforcement of the Biden administration’s vaccine mandate for private employers after a federal court blocked the measure. The OSHA website page dedicated to the COVID Vaccine Emergency Temporary Standard (ETS) reads: “While OSHA remains confident in its authority to protect workers in emergencies, OSHA has suspended activities related to the implementation and enforcement of the ETS pending future developments in the litigation.” Last week, the U.S. Court of Appeals for the Fifth Circuit fully blocked Biden’s executive order requiring companies with over 100 workers to mandate vaccination for their employees after temporarily staying it on November 12.
The court ordered that OSHA “take no steps to implement or enforce” the vaccine mandate “until further court order.” By its mandate, the Biden administration is claiming that the federal government, through congressional legislation, has regulatory power to issue a medical mandate for the sake of public health and therefore general welfare. However, since the directive was announced, many legal scholars have challenged its constitutionality, given that the legislation it relies on for authority explicitly states that an ETS can only be issued when employees are exposed to a “grave danger” that necessitates immediate action. That case is becoming increasingly difficult to argue, given the fact that some vaccinated individuals can transmit the disease and that treatment options for COVID infections are expanding.
As of Tuesday, the Biden administration is planning to purchase 10 million doses of Pfizer’s antiviral medication to treat patents with COVID. Some lawmakers and pundits have speculated that Biden’s strategy with the vaccine mandate recognized that the order would likely be indefensible in court but hoped that its chilling effect would pressure employers to comply in advance of any litigation. After the federal appeals court first issued a motion to stay the order, White House Press Secretary Jen Psaki still urged employers to implement coercive measures to increase vaccination numbers among their labor forces, although without the teeth of government enforcement.
It took 108 days to approve the vaccine. It will take over 20,000 days to tell us why.
The FDA has asked a federal judge to make the public wait until the year 2076 to disclose all of the data and information it relied upon to license Pfizer’s COVID-19 vaccine. That is not a typo. It wants 55 years to produce this information to the public. As explained in a prior article, the FDA repeatedly promised “full transparency” with regard to Covid-19 vaccines, including reaffirming “the FDA’s commitment to transparency” when licensing Pfizer’s COVID-19 vaccine. With that promise in mind, in August and immediately following approval of the vaccine, more than 30 academics, professors, and scientists from this country’s most prestigious universities requested the data and information submitted to the FDA by Pfizer to license its COVID-19 vaccine.
The FDA’s response? It produced nothing. So, in September, my firm filed a lawsuit against the FDA on behalf of this group to demand this information. To date, almost three months after it licensed Pfizer’s vaccine, the FDA still has not released a single page. Not one. Instead, two days ago, the FDA asked a federal judge to give it until 2076 to fully produce this information. The FDA asked the judge to let it produce the 329,000+ pages of documents Pfizer provided to the FDA to license its vaccine at the rate of 500 pages per month, which means its production would not be completed earlier than 2076. The FDA’s promise of transparency is, to put it mildly, a pile of illusions.
It took the FDA precisely 108 days from when Pfizer started producing the records for licensure (on May 7, 2021) to when the FDA licensed the Pfizer vaccine (on August 23, 2021). Taking the FDA at its word, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure. While it can conduct that intense review of Pfizer’s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public. So, let’s get this straight. The federal government shields Pfizer from liability. Gives it billions of dollars. Makes Americans take its product. But won’t let you see the data supporting its product’s safety and efficacy. Who does the government work for?
What happened to the story of puppies eaten alive?
COVID-19 booster shots may become the new standard to be considered fully vaccinated, according to the nation’s top doctor. Dr. Anthony Fauci discussed the impending need for hundreds of millions of Americans to roll up their sleeves and get the jab during a pre-taped interview that aired at the 2021 STAT Summit in Boston this week, according to ABC News. “I happen to believe as an immunologist and infectious disease person that a third shot boost for an mRNA [vaccine] … should be part of the actual standard regimen, where a booster isn’t a luxury,” the director of the National Institute of Allergy and Infectious Diseases reportedly said.
“A booster isn’t an add-on and a booster is part of what the original regimen should be. So that when we look back on this, we’re going to see that boosters are essential for an optimal vaccine regimen,” Fauci told the audience, according to the network. The remarks came as New York City and several states expanded booster shot eligibility to all adults who were vaccinated against COVID-19 at least six months ago this week. Until then, the jabs were only available to people 65 years of age and over and those in high-risk situations. The guidance from the president’s chief medical advisor came as Moderna filed an application with the FDA seeking emergency use authorization of vaccine booster shots for all US residents 18 and older. Pfizer last week asked federal regulators to expand its booster shot eligibility to all Americans.
Some 31.5 million Americans had already received a booster shot on Wednesday, according to CDC data. More than a third of the recipients were over 65. The number of vaccinated US residents stood at 196 million people, according to the agency — which noted that more than 40 percent of the country was not fully inoculated. The push for booster shots came as the seven-day rolling average of cases increased by 27 percent since Oct. 25, US data showed. Fauci had said over the summer he was “certain” Americans would need additional doses of COVID-19 vaccines.
They, too, have a deal with Pfizer.
On Friday, November 12, 2021, Sentara Hospital System in Virginia submitted a motion to dismiss the complaint filed against it earlier in the week by Dr. Paul Marik—co-chief medical officer of the FLCCC, tenured professor, and the Director of the Intensive Care Unit at Sentara Norfolk General Hospital. Dr. Marik filed suit seeking a temporary injunction to lift the ban Sentara Healthcare System had placed on a range of highly effective COVID-19 treatments used by Dr. Marik to save critically ill COVID-19 patients. These components, including IV vitamin C, dutasteride, fluvoxamine, finasteride, and ivermectin, had previously been successfully used—with the exception of ivermectin, the use of which Sentara never permitted —to reduce COVID deaths in the ICU by as much as 50 percent. The result of the prohibition has been a sharp increase in mortality at Sentara Norfolk General Hospital.
The hospital’s motion to dismiss Marik’s lawsuit rests on their claim that Dr. Marik has “lack of standing” to bring the lawsuit against the hospital. According to the hospital, “The alleged causes of action against Sentara, if any, reside with the patients in the hospital, not those patients’ attending physician.” The hospital also asserted in its motion that Virginia’s Advance Directive Statute and/or the Health Care Decisions Act do not “afford the patient the ability to specifically direct or demand his or her course of treatment by a physician or hospital.” But Dr. Marik’s complaint argues that “Sentara’s prohibition of these medicines is causing needless deaths, because it violates patients’ rights to informed consent, and because it contravenes Virginia’s Health Care Decisions Act.”
Under Virginia law, Dr. Marik, as the “attending physician” of his patients in the ICU, is personally and legally responsible for the exercise of professional skill and judgement in determining what a patient under his care receives. Because Dr. Marik is prohibited from giving his patients medications that are potentially lifesaving—and have been demonstrated as such in peer-reviewed studies—he is forced to abandon his professional duty. His actions are regulated by the hospital in such a way that it causes him to violate the rights of his patients.
The hospital’s motion to dismiss or continue the hearing — scheduled for Thursday, November 18 at 1PM ET in Norfolk — also argues that Dr. Marik has lack of standing to bring the lawsuit because he has not been “injuriously affected” by the prohibition of the medications since he himself was not a patient who was denied “the alleged” lifesaving treatment. Yet, if Dr. Marik were to violate the hospital’s prohibition, he would be subject to revocation of his hospital privileges. Furthermore, due to Sentara’s prohibition, he is the one who faces potential legal liability for failing to provide his patients with the medications which, in his professional judgment, had the capacity to save their lives. Therefore, Dr. Marik has solid standing to seek vindication of the rights of his patients and of himself as treating physician.
Think there’s a supply chain issue now? Just wait.
A very interesting interview with Chris Spear, president and CEO of the American Trucking Association. During a House Transportation Committee hearing on supply chain issues, CEO Chris Spear shares an internal survey showing that 37% of truck drivers “not only said no, but said hell no” to the Biden vaccine mandates. To give some perspective of the downstream consequence, the ATA President noted that “if just 3.7 percent, not 37 percent, just 3.7 percent” of the drivers left the industry, there would be over a quarter million vacancies resulting in a “catastrophic” collapse of the U.S. supply chain. Mr. Spear also shared his opinion the OSHA rule is completely unworkable and unlawful.
The consequences are grave if just 3.7% did not work. However, if ten times that many, 37 percent of truck drivers, stopped hauling products because of the Biden vaccine requirement, American civic society would collapse within days as panicked citizens took to the streets. Desperate Americans would be clamoring for scarce products, and the impact on society could not be measured. As we have continued to point out, a federal vaccine mandate might sound like a good idea on a think tank, academic or white paper policy level of consideration; but on a practical level, wiping out a large percentage of your most productive workforce over a vaccine mandate is unworkable, and might even end the operation of the entire business.
It is important to note the recent NBC poll on this issue amid the outlook of the vaccine mandates. A majority of the country do not support the vaccine mandates, and worse still, the number of unvaccinated workers is essentially unwavering in the past six weeks. Remember, the number of Americans who willingly quit their jobs increased to 4.3 million in August, and then increased again to 4.4 million in September. People are not f**king around now.
Challenging the spike protein monopoly?
The development of mRNA vaccines, a long-promised and much-touted biotechnology, is regarded as a great victory of medical research spurred by the COVID-19 pandemic. Nowadays, millions of people have been inoculated with these novel vaccines, which comprise both the Pfizer/BioNTech shot as well as Moderna’s COVID-19 vaccine. Yet mRNA vaccine technology is not the only immunological innovation that may emerge from the pandemic. Now, a company based in the United Kingdom called Emergex is preparing to test a next-generation COVID-19 vaccine based on a radical new technology. Unlike the messenger RNA (mRNA) vaccines — which inject a bespoke strand of messenger RNA that generates Spike proteins within the human body — this new vaccine technology is delivered via a skin patch, and relies on T cells, which are white blood cells that are part of the immune system, to kill infected cells.
It is believed that a T-cell vaccine would incite a more rapid and durable response to fighting the infection. “Although current COVID-19 vaccines have made significant progress in reducing mortality and morbidity, challenges still remain, especially with the development of new variants,” said Professor Blaise Genton, Principal Investigator for the trial from the Center for Primary Care and Public Health (Unisante) at the University of Lausanne, Switzerland. “This exciting new scientific approach to developing a vaccine against SARS-CoV-2 addresses the need to generate a T-cell response to elicit long term immunity.”
One of the constituent types of immune system cells, T cells play a vital role in fighting threatening foreign substances in the human body. Unlike some immune system cells, T cells do not attack any foreign body; rather, they are laser-focused only on specific pathogens. This trait, researchers believe, could be exploited such that their vaccine could instill a T-cell response in the human body — without actually giving their immune system the dangerous SARS-CoV-2 virus first. Emergex’s proposed vaccine would prepare T cells to remove infected cells from the body right after being infected. This would prevent the virus from replicating and progressing to COVID-19. By targeting and priming the T cells, this would also reduce the transmissibility between infected and non-infected people because it would stop the virus from replicating and prevent the onset of symptoms.
Closer to exploding than almost anyone appears to think.
A USA Today poll shows that Biden’s approval has sunk to 38%. The trend line here is truly devastating. We can speculate why. Inflation plays a role. But also the vaccine mandate seems to have hit the Biden approval rating very hard. In the coming month, millions of jobs could be affected by this. The protests are growing in every city, and the people protesting are union members, city employees and even tech workers. They are furious that government would presume the right to tell people what medicines they must inject into their bodies. Some of the protesters are themselves vaccinated against their will. They are bitter and angry about it. The news of adverse outcomes from vaccination is leaking out through family networks and alternative news venues, though it continues to be suppressed by the media. So this mandate is now being seen as a direct threat to individual health.
That’s something that will inspire people to take to the streets. The 5th Circuit Court of Appeals has issued a stay against OSHA’s mandate on businesses. The Biden administration attempted a response, but the result was lame. It just said that it stands by the mandate on health grounds, period. Perhaps this won’t surprise you, but the president himself instructed businesses to go ahead and proceed, essentially advocating that they ignore the court ruling. In other words, the Biden administration has gone completely lawless, not just ignoring the U.S. Constitution but also advocating that businesses ignore the courts. That’s dangerously close to announcing that we now live with dictatorship. It’s no wonder that even Sen. Ted Cruz of Texas is talking about secession from the union. If he is saying this, I truly cannot imagine the kind of anger there is among the citizens.
If you wanted to live in exciting times, you chose a great time to be alive. The conditions are ripe not only for continuing electoral bloodbaths but more street protests, explosive town halls, hate-filled school board meetings and much worse. A more divisive and destructive policy is hard to imagine. Sadly, these policies are dividing friends and family. Some people with vaccinations don’t see the big deal here. Just get the jab, they say, and then you can be free. Others find this idea to be outrageous, an immoral acquiescence to power that can only lead to even worse outcomes. I just watched several hours of testimony from big shots at the NIH and the CDC. It might as well have been a paid advertisement from Moderna and Pfizer. Nearly every word out of the bureaucrats’ mouths was structured to push the vaccines that most everyone knows by now have failed to live up to their promise.
Indeed, if they were as good and safe as they say, government would not need to mandate them. The mandates, ironically, undermine public confidence. It’s hard to imagine that public confidence in everything could fall further, but it will. To top it off, making all the above much worse, the vaccination is now coming for the kids. Mandates will surely follow. You want revolution in this country? This is a good way to foment one. The current regime has another year of unchecked power. It seems unfathomable. So far, they have not been deterred by anything, not the courts, not public opinion, not even sinking election prospects. The U.S. has become a powder keg.
The prejudice will be needed, or the whole circus can start again.
During the Kyle Rittenhouse trial, the prosecution argued that Kyle provoked the men who attacked him by waving his gun. To prove this, during the trial, the prosecution gave the defense fuzzy drone footage. There was a great deal of argument about what could be extrapolated from that fuzzy view. It turns out that the prosecution had within its possession a high-quality video that it played for the judge after the trial ended. On this, and other evidentiary grounds, the defense moved for a mistrial with prejudice. The defense motion states the facts with sufficient clarity that I’m going to reprint them here verbatim:
“On November 5. 2021, the fifth day of trial on this case, the prosecution turned over to the defense footage of a drone video which captured some of the incident from August 25, 2020. The problem is, the prosecution gave the defense a compressed version of the video. What that means is the video provided to the defense was not as clear as the video kept by the state. The file size of the defense video is 3.6 MB and the state’s is 11.2 MB. Further, the dimensions on our video are 480 x 212, the state’s, 1920 x 844. The video which was in the state’s possession, wasn’t provided to the defense until after the trial concluded. During the jury instructions conference, the defense played their version of the video for the court to review. The state indicated their version was much clearer and had their tech person come into court to have the court review their clearer video. The video is the same; the resolution of that video, however, was not. The state did not provide their quality video to the defense until Saturday, November 13, 2021, and only did so upon specific request by Attorney Wisco — two days before closing arguments and after the evidence had been closed.”
Under Wisconsin law, when the defense makes a demand, the prosecution must provide to the defense “[a]ny physical evidence that the district attorney intends to offer in evidence at the trial” and “[a]ny exculpatory evidence.” That’s Wisconsin Stat. § 971.23(1)(g) & (h). I don’t have the time to research the law, but my bet is that if Wisconsin’s appellate court ever had before it the question of whether the prosecutor may get away with producing bastardized, degraded versions of the requested evidence, it would say emphatically not. The motion for a mistrial with prejudice also raises the fact that, when Kyle Rittenhouse took the witness stand, the prosecutors improperly accused him of keeping silent after his arrest. That right, of course, is enshrined in the famous Miranda rights warning that all arrestees in America receive: “You have the right to remain silent …” The corollary to that right is that this silence cannot be used against the defendant in a court of law, but that’s exactly what the prosecution tried to do.
“Schiff’s spin is enough to cause permanent vertigo.”
The famous philosopher and mathematician Blaise Pascal once declared that “the only shame is to have none.” The problem with shame is that it requires a sense of guilt over one’s actions. In the age of rage, there appear fewer and fewer actions that are beyond the pale for politics. Take Adam Schiff and the Steele dossier. While even the Washington Post has admitted that it got the Russian collusion story wrong in light of the findings of Special Counsel John Durham, House Intelligence Committee Chair Adam Schiff, D-Calif., is still insisting that he was absolutely right to promote the discredited Steele dossier. Schiff’s interview on NBC’s Meet the Press may be the final proof of the death of shame in American politics.
Schiff was one of the greatest promoters of the Steele dossier despite access to briefings casting doubt about Steele and the underlying claims. However, Schiff recently has attempted to defend himself by claiming that Steele was a respected former spy and that he was lied to by a Russian source. Schiff told host Chuck Todd: “I don’t regret saying that we should investigate claims of someone who, frankly, was a well-respected British intelligence officer. And we couldn’t have known, of course, years ago that we would learn years later that someone who is a primary source lied to him. [Igor] Danchenko lied to Christopher Steele and then lied to the FBI. He should be prosecuted. He is being prosecuted. And I’ll tell you this, if he’s convicted, he should not be pardoned the way Donald Trump pardoned people who lied to FBI agents, like Roger Stone and Mike Flynn. There ought to be the same standard in terms of prosecuting the liars. But I don’t think there ought to be any pardon, no matter which way the lies cut.”
Schiff’s spin is enough to cause permanent vertigo. Some of us have spent years being pummeled for questioning the obvious problems with the Steele dossier, including the long-denied connection to the Clinton campaign. Schiff was the main voice swatting down such criticism and his endorsements were treated as dispositive for media from MSNBC to the Washington Post. After all, he was the chair of the House Intelligence Committee and assured the public that our criticisms were meritless and the dossier was corroborated. Schiff’s spin, however, continues to deny the obvious about the Russian collusion scandal.
First, many would guffaw at the claim that Steele was and remains a “well-respected British intelligence officer.” Soon after the dossier was shopped to the FBI, British intelligence flagged credibility problems with Steele. The FBI severed Steele as an asset. Even his own sources told the FBI that Steele wildly exaggerated information and distorted intelligence. Most recently, Steele went public with a laughable claim that Michael Cohen, Trump’s former counsel, was lying to protect Trump despite spending years trying to get Trump charged criminally.
Second, Schiff ignored repeated contradictions in Steele’s dossier as well as evidence that the dossier was paid for and promoted by the Clinton campaign. In 2017, even fired FBI agent Peter Strzok admitted that “we are unaware of ANY Trump advisors engaging in conversations with Russian intelligence officials” and “Steele may not be in a position to judge the reliability of his subsource network.” Schiff would have had access to some of this intelligence. Indeed, while the Clinton campaign was denying that it funded the dossier, American intelligence knew that that was a lie. Indeed, until the Durham indictments, Schiff continued to defend the Russian collusion investigation and the Steele dossier.
Third, Schiff attempts to portray the sole problem with the Steele dossier as Russian analyst Igor Danchenko. That is simply not true. Schiff was long aware that there were allegations of misleading or false information given by the FBI to the secret court. Indeed, the first Durham conviction was of Kevin Clinesmith, the former FBI agent who pleaded guilty. Schiff was aware that President Barack Obama was briefed in 2017 that Hillary Clinton was allegedly planning to manufacture a Russian collusion scandal — just days before the start of the Russian investigation. The dossier was riddled with disproven allegations. Fourth, Schiff states that he merely sought to investigate allegations. However, Schiff was one of the most active members fueling the Russian collusion allegations. Indeed, when the Mueller investigation found no proof of Russian collusion, Schiff immediately went public to claim that he had evidence of collusion in his committee files. It was meant to keep the scandal alive. Schiff has never produced his promised evidence of collusion.
Kill the Bill
It's 2 years of labeling us as lunatics, us, standing up for the core values of our ancestors. Wake up! pic.twitter.com/rW2LiAtP64
— Wake Up From COVID (@wakeupfromcovid) November 17, 2021
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