Alberto Giacometti Tête Noire 1957
“..by the CDC’s own data, we are seeing a 12,000 percent increase in deaths with these vaccines and they’re still talking about giving this to our kids.”
A group of parents, along with America’s Frontline Doctors (AFLDS) and written by Thomas Renz, Esq., filed a motion in federal court seeking a temporary restraining order “to prevent the expansion of the FDA’s Emergency Use Authorization (EUA) for COVID-19 vaccines to include children under the age of 16,” according a statement released earlier today. The motion was filed in the U.S. District Court for the Northern District of Alabama and is directed against Secretary Xavier Becerra and the Department of Health and Human Services (HHS). It consists of numerous plaintiffs representing various interests and backgrounds, including “physicians and the parents of minor children who are alarmed about offering children experimental products that have not undergone long term animal or safety studies.”
“We’ve never seen this level of side effects for any vaccine without the FDA taking action,” stated Dr. Angelina Farella, AFLDS Pediatric Medical Director. “The Rotavirus vaccine was pulled for 15 cases of non-lethal side effects and the Swine Flu vaccine was pulled for 25 deaths. But now, by the CDC’s own data, we are seeing a 12,000 percent increase in deaths with these vaccines and they’re still talking about giving this to our kids.” “Our children should never be the experiment,” she continued. “No additional authorizations or mandates should be granted. We want to preserve the previously established safety standards.” Dr. Farella also cited statistics from the Centers for Disease Control and Prevention (CDC), which confirms “children are at statistically zero risk for COVID-19, making expansion of the EUA for younger children medically unnecessary.”
If dogs can smell it in a minute…
A one-minute Covid-19 breath test has received provisional authorization in Singapore, where it will be used to test people coming into the country from Malaysia. The National University of Singapore’s Breathonix test – which was developed from “cancer detection technology” – can detect Volatile Organic Compounds in a person’s breath to see if they are healthy or not, researchers say, though the test will also be used alongside more traditional antigen rapid testing. In partnership with the Singapore Ministry of Health, Breathonix will first deploy its testing at the Tuas Checkpoint, which connects Singapore and Malaysia.
Breathonix’s test was previously trialed at Changi Airport, the National Centre for Infectious Diseases, and in Dubai, and the breathalyzer technology is unlikely to cause any cross-contamination, according to its founders. “Our breath test is non-invasive. Users only need to breathe out normally into the disposable mouthpiece provided, so there will not be any discomfort,” Breathonix CEO Dr. Jia Zhunan said. “Cross-contamination is unlikely as the disposable mouthpiece has a one-way valve and a saliva trap to prevent inhalation or saliva from entering the machine.” The test will likely be the fastest in the world upon its rollout and could be a gamechanger in places where fast results are necessary, including airports and borders.
Health care or sick care?
The entire pharmaceutical industry spent just $83 billion on R&D in 2019. That sounds like a lot of money, but it isn’t when you look at the federal budget, even confining it just to Medicare. Indeed, there’s a serious problem here in that most of this spending is on biologics in what is called the “specialty drug” category. These are large-molecule, hard-to-make things that treat complex, rare or chronic conditions. But not too rare: Nobody will spend a billion dollars to develop a drug that only helps a thousand people at best, as the price just to cover the development expense is over a million dollars a person. The bottom line is that the system we have today has incentivized the development of large-molecule, expensive and complex drugs that are ridiculously expensive and aimed at complex and rare conditions — defined as a small body of people, but not too small.
Fall on the wrong side of the “too small” line and you get nothing. Become to easy to look at where someone will take a crack at synthesizing something simple that might work and again you get nothing. Once in a while this winds up in the news or even generates lawsuits but only when it’s a large group impacted, as was the case with Sovaldi. If it wasn’t for the wide prevalence of Hepatitis C, driven by IV drug abuse, nobody would have bothered to chase that and the drug companies know it. In addition there’s a secondary perverse incentive which is that inevitably fatal and rapidly degenerative diseases are targeted preferentially. The reason is safety standards; nobody would tolerate a headache medicine that killed 1 in 1,000 users, but a cancer medicine that does so is acceptable because without treatment you’re going to die for certain, and any chance of living is better than none.
Many drugs and other therapies developed over the last decades have, in fact, been frauds to at least some degree. It is not that they don’t work; most of them do. It is that they displace other working therapies without demonstrating a cost:benefit increment and, in many cases, wind up being more harmful that either the alternative or having no better benefit. But in every case they are more-expensive. The most-outrageous are “re-label” events such as what happened with Albuterol inhalers in which the propellant, but not the active ingredient, was changed and then it was re-patented screwing asthma sufferers out of billions of dollars. What’s happened with Covid-19 is a wildly-blinding illustration of the problems. There was an immediate target for one intervention against Covid-19 – inoculation. But inoculations take ten or more years to develop, and the reason is simply that many of the longer-term side effects take that long to find. Something that results in a negative cross-reaction with the original virus over time or other viruses in the environment cannot, in humans, be “challenge trialed” because the potential outcome is death. So all you can do is look for safety signals over a long period of time in a small number of people.
Yes, you do animal work first to identify potential threats in that realm, but you can’t be exhaustive and many viruses will not infect the animal used for testing, so your ability to screen is limited. In addition there are all manner of other things that show up that are very bad, including autoimmune disorders, and again those almost always take years to develop. Finally there is no way to reasonably do regular blood work and such on large groups; it simply costs too much money. But any such signal generated is important so you want to do those on small groups where intensive laboratory analysis can be done on each and every participant to catch any indication that a problem may be present but not instantly obvious via presented symptoms. You can’t do this across 30,000 people, say much less 150 million. But you can do it across 1,000 people and you damn well should have to for a couple of years as a risk-limiting corral when the eventual result is something you cannot take back if it turns out to be seriously harmful.
Interesting from our Comments section yesterday,
For COVID-19 mRNA Vaccine (Pfizer or Moderna), the biodistribution studies in animals were not conducted. The surrogate studies with luciferase and solid-lipid nanoparticles (Pfizer) confirm a biodistribution to the liver and other body tissues beyond the administration site . For Moderna, the biodistribution of mRNA-1647 (encoding CMV genes) formulated in a similar lipid nanoparticulate delivery system confirms a biodistribution beyond the injection site, in particular, the distribution to the lymph nodes, spleen and the eye was noted . However, the detailed tissue-specific distribution of mRNA vaccines encoding SARS-CoV-2 spike proteins (Pfizer or Moderna) is not fully known that can offer invaluable insights into the potential safety of these vaccines in people with pre-existing conditions or those on certain medications.
The detailed biodistribution data including pharmacokinetics of various CoViD vaccines were not conducted by the vaccine manufacturers because the studies demonstrating biodistribution of antigens were considered ‘not required’ by the regulatory authorities on the premise that vaccines work by an immunological response than the classic pharmacological approach. However, such an exemption may barely justify the conventional vaccines such as those incorporating whole inactivated virus, split virion, or the sub-unit vaccines, that directly attracts an immune response post-injection.
On the contrary, modern genetic vaccines work on the premise of gene delivery, therefore, a detailed biodistribution and pharmacokinetic evaluation of the formulated product is invaluable in understanding the potential impact of vaccine encoding gene transfection to various body tissues beyond the site of injection. Vaccines are one of the great discoveries in medicine that has improved life expectancy dramatically. However, if genetic vaccines were to be sustained beyond the CoViD19 pandemic, a tissue targeted approach may be the way forward to limit the antigen (the encoding gene) distribution to the intended tissues only to improve the vaccine safety profile for a global mass public rollout. In comparison, the conventional vaccine approaches (classic non-genetic formulations) have a long history of human use across much wider age groups (infants to elderly) and have an established safety profile despite the current challenges in antigen propagation and large-scale production in a timely manner using conventional methods.
“..will anyone be held responsible for the thousands who died because of the prohibition on safe treatments such as hydroxychloroquine and Ivermectin that have since been shown to be effective against Covid-19? ”
not only did the doom and gloom predicted by the lockdown fanatics fail to materialize, but the steady, seasonal downward trend of the virus toward extinction continued regardless of government action. As we have repeated for a year on the Liberty Report, the virus was going to virus regardless of anything we did about it. And Texas proved it. However, some very important questions remain to be answered as the Covid panic across the United States is finally starting to recede. First, will anyone be held responsible for the thousands who died because of the prohibition on safe treatments such as hydroxychloroquine and Ivermectin that have since been shown to be effective against Covid-19?
As soon as Donald Trump mentioned that hydroxychloroquine might be effective against the virus, the “experts” circled the wagons. It was banned for use, until it later was quietly un-banned. The politicization of medicine is anti-science, anti-human, and anti-American. Will those who needlessly died due to this politicization finally get their justice? Second, though Abbott deserves credit for taking the bold step, shouldn’t he be held accountable for closing the state in the first place? After all, when someone has been punching you in the face and then they stop, do you thank them for letting up or do you ask why they punched you in the first place? Will all the tyrannical rule-by-decree orders across the United States be stricken from the books?
Or will they just be allowed to do this again for any reason they choose? Third, thanks to Senator Rand Paul, we are now all aware of Dr. Fauci’s role in funding gain-of-function research on viruses in China. Will we be able to find out exactly why we are being forced to pay for the mad scientist research into how to create more deadly viruses? Can we opt-out of this funding?
“..left the FDA in April 2019 and now sits on the board of Pfizer..”
Scott Gottlieb, the former head of the Food and Drug Administration (FDA), said Monday that there is growing circumstantial evidence suggesting that COVID-19 may have originated in a lab and not in nature. CNBC’s “Squawk Box” co-host Rebecca Quick asked Gottlieb what he made of a Wall Street Journal article published Sunday that said three employees at the Wuhan Institute of Virology had sought hospital treatment for flu-like symptoms around the same time COVID-19 began to emerge in China. “I think the challenge right now is that the side of the ledger that supports the thesis that this came from a zoonotic source, from an animal source, hasn’t budged. And the side of the ledger that suggests this could have come out of a lab has continued to grow,” said Gottlieb, who left the FDA in April 2019 and now sits on the board of Pfizer.
“People a year ago who said this probably came from nature, it’s really unlikely it came from a lab, maybe a year ago that kind of a statement made a lot of sense because that was the more likely scenario,” Gottlieb added. He said the source of COVID-19 has yet to be identified and noted that the origins of related diseases were usually identified at this point following the initial outbreak. “It’s not for lack of trying. There has been an exhaustive search,” Gottlieb said of COVID-19. “I don’t think we’re ever going to get to the bottom of this,” he added. “Because unless we have a whistleblower — assuming it did come out of a lab, and I’m not saying it did, but assuming it did — unless we have a whistleblower or a regime change in China, you’re not going to truly find out.”
“The news business just can’t stop clowning itself.”
The news business just can’t stop clowning itself. The latest indignity is an international fact-checking debacle originating, of all places, at a “festival of fact-checking.” The Poynter Institute is perhaps the most respected think tank in our business, an organization seeking to “fortify journalism’s role in a free society,” among other things through its sponsorship of the fact-checking outlet PolitiFact. A few weeks back, it held a virtual convention called the “United Facts of America: A Festival of Fact-Checking.” The three-day event featured special guests Christiane Amanpour, Dr. Anthony Fauci, Brian Stelter, and Senator Mark Warner — a lineup of fact “stars” whose ironic energy recalled the USO’s telethon-execution of Terrance and Phillip before the invasion of Canada in South Park: Bigger, Longer, and Uncut. Tickets were $50, but if you wanted a “private virtual happy hour” with Stelter, you needed to pay $100 for the “VIP Experience.”
During the confab, PolitiFact’s Katie Sanders asked Fauci, “Are you still confident that [Covid-19] developed naturally?” To which the convivial doctor answered, “No, I’m not convinced of that,” going on to say “we” should continue to investigate all hypotheses about how the pandemic began: Conservatives in particular were quick to point out that Fauci last year said, “Everything about the stepwise evolution over time strongly indicates that [this virus] evolved in nature and then jumped species.” At that time last May, of course, the issue of the pandemic’s origin had already long since been politicized, with Donald Trump’s administration anxious to point a finger at China for causing the disaster. Mike Pompeo went so far as to say there was “enormous evidence” the disease had been created at the Wuhan Institute of Virology. Fauci was touted as a hero for pushing back on this and many other things.
Fauci’s new quote about not being “convinced” that Covid-19 has natural origins, however, is part of what’s becoming a rather ostentatious change of heart within officialdom about the viability of the so-called “lab origin” hypothesis. Through 2020, officials and mainstream press shut down most every discussion on that score. Reporters were heavily influenced by a group letter signed by 27 eminent virologists in the Lancet last February in which the authors said they “strongly condemn conspiracy theories suggesting that COVID-19 does not have a natural origin,” and also by a Nature Medicine letter last March saying, “Our analyses clearly show that SARS-CoV-2 is not a laboratory construct.”
The consensus was so strong that some well-known voices saw social media accounts suspended or closed for speculating about Covid-19 having a “lab origin.” One of those was University of Hong Kong virologist Dr. Li-Meng Yan, who went on Tucker Carlson’s show last September 15th to say “[Covid-19] is a man-made virus created in the lab.” After that appearance, PolitiFact — Poynter’s PolitiFact — gave the statement its dreaded “Pants on Fire” rating.
What would you expect from the MSM?
A retired New York Times science editor has slammed the mainstream media for ignoring the possibility that coronavirus leaked from a laboratory in Wuhan and accused journalists of falling for ‘Chinese propaganda’ instead of doing their own research. Nicholas Wade, who penned a 1,100-word article examining the link entitled ‘The origin of COVID: Did people or nature open Pandora’s box at Wuhan?’ earlier this month, took aim at top news outlets in a Fox News interview on Sunday night. He claimed the media mainstream media failed to ‘take off its political glasses’ to investigate the virus’ origins, the facts of which, he said, are being obscured by the Chinese Communist Party.
Wade’s remarks come as more scientists and political officials are coming forward to support the theory that the virus may have been developed in a Chinese laboratory and was covered up – after scoffing at the idea for much of the past year in part because it was pushed by then-President Donald Trump. Among the top officials now speculating that possibility is Dr Anthony Fauci, who recently said he’s ‘not convinced’ the virus formed naturally after repeated statements to the contrary. The case for a lab leak was strengthened on Sunday when a previously-undisclosed US intelligence report revealed three researchers from China’s Wuhan Institute of Virology (WIV) sought hospital care in November 2019 – months before China disclosed the COVID-19 outbreak.
‘I think we see a sustained Chinese propaganda effort at work,’ Wade, who served as the staff writer for the Science Times section of the New York Times from 1982 to 2012, told Mark Levin on Life, Liberty & Levin. ‘But, you know, more than that, it was just the blindness, if I could put it that way, of our media — we’re too polarized to see scientific issues for their own sake without putting a political gloss on them,’ he continued. ‘We don’t know for sure: The origin of the virus is just we’ve got these two possible scenarios. But if you look at all the evidence and ask yourself, well, which scenario explains all these facts better on present evidence, it seems, to me at least, that the lab-escape hypothesis explains it a lot better. ‘But it’s a sort of complicated conclusion to arrive at, and I can only assume that the media was blindsided, they didn’t do the work that was necessary.’
Complete insanity. Shutting down discussion, which Facebook should encourage.
Project Veritas has obtained internal documents from Facebook whistleblowers detailing the social media platform’s efforts to censor COVID-19 vaccine concerns. Two of the Facebook insiders have come forward with leaked company documents detailing the Big Tech giant’s plan to curb and police “vaccine hesitancy” (VH) worldwide through surreptitious “comment demotion.” “They’re trying to control this content before it even makes it onto your page before you even see it,” one of the Facebook insiders said to Project Veritas. “If I lose my job, it’s like, what do I do? But that’s less of a concern to me.” The stated goal of the global feature is to “reduce user exposure” to VH comments. Another aim of the program is to “decrease” other engagement of VH comments including “create, likes, reports [and] replies,” according to Project Veritas.
One of the Facebook whistleblowers said the company uses a tier system to rank and determine how comments should be censored or buried. This is all based on how much the statements question or caution against the COVID-19 vaccination. Tier 2, for instance, represents “Indirect Discouragement” of getting vaccinated. User comments such as these would be “suppressed,” Project Veritas reported. Comments that include “shocking stories” that describe what could be true events or facts that can raise safety concerns are demoted. Any of the such that raises concern about coronavirus vaccinations are fair game to be demoted and hidden, according to the source, despite authenticity or capacity to contribute to the public good. “I have to do something,” one of the Facebook insiders said.
It doesn’t matter if the comments are true, factual, or represent reality. The comment is demoted, buried, and hidden from public view if it clashes with the system. “It doesn’t match the narrative,” one source explained. “The narrative being, get the vaccine, the vaccine is good for you. Everyone should get it. And if you don’t, you will be singled out.” One of the insiders, a data center technician, showed documentation detailing an algorithm test being run on 1.5 percent of Facebook and Instagram’s almost 3.8 billion users worldwide. “They’re trying to control this content before it even makes it onto your page before you even see it,” one insider said.
“Ordinary Americans, not Big Tech, have been footing the bill for those costs. Yet Big Tech derives tremendous value from these high-speed networks.”
Up to now, there have been two leading approaches. The first is the FCC’s current model for funding internet builds. Many consumers are unaware that the federal government collects roughly $9 billion a year through a tax on their monthly bills for traditional telephone service—both wireless and wireline. The FCC then uses that pot of money, known as the Universal Service Fund, to support internet builds in rural areas and on other efforts to close the digital divide. This model made sense when Congress established it back in 1996. But it is now hopelessly outdated. The dominant platform for communications has shifted from the telephone network to the internet.
Indeed, the revenue base associated with the traditional telephone network has fallen sharply from a peak of around $80 billion in the 2000s to less than $30 billion today as more and more services—including those now offered by Big Tech—are delivered over the internet instead. Yet we continue to rely on that shrinking base of revenues from the telephone network to fund the broadband network. This is like taxing horseshoes to pay for highways. This antiquated system is on the verge of collapse. The FCC has kept it on life support by increasing the tax on consumers’ telephone bills at an accelerating clip. Indeed, that tax recently surged above 30 percent for the first time. This is not sustainable; relying on this model to fund additional infrastructure would strain the system well past its breaking point.
Big Tech has been enjoying a free ride on our internet infrastructure while skipping out on the billions of dollars in costs needed to maintain and build that network. Indeed, one study shows that the online streaming services provided by just five companies—Netflix, YouTube, Amazon Prime, Disney+ and Microsoft—account for a whopping 75 percent of all traffic on rural broadband networks. The same study shows that 77-94 percent of total network costs are related to adding capacity or otherwise supporting the delivery of those streaming services. Ordinary Americans, not Big Tech, have been footing the bill for those costs. Yet Big Tech derives tremendous value from these high-speed networks. Indeed, Facebook, Apple, Amazon, Netflix and Google generated nearly $1 trillion in revenues in 2020 alone—an almost 20 percent increase over the prior year.
It would take just 0.009 percent of those revenues to eliminate entirely the unsustainable 30 percent tax that currently hits consumers on their monthly bills. Ending this corporate welfare is more than fair. It is consistent with the network compact that has prevailed since the earliest days of the Ma Bell telephone network. Historically, the businesses that derived the greatest benefit from a communications network paid the lion’s share of the costs. For instance, the fees that businesses paid for local and long-distance calls provided the key funding stream to build the traditional telephone network.
As I remembered yesterday. Greenwald’s memory has the details.
There is little doubt that the forced landing of this plane by Belarus, with the clear intention to arrest Protasevich, is illegal under numerous conventions and treaties governing air space. Any forced landing of a jet carries dangers, and safe international air travel would be impossible if countries could force planes flying with permission over their air space to land in order to seize passengers who might be on board. This act by Belarus merits all the condemnation it is receiving. Yet news accounts in the West which are depicting this incident as some sort of unprecedented assault on legal conventions governing air travel and basic decency observed by law-abiding nations are whitewashing history. Attempts from U.S. officials such as Blinken and E.U. bureaucrats in Brussels to cast the Belarusians’ behavior as some sort of rogue deviation unthinkable for any law-respecting democracy are particularly galling and deceitful.
In 2013, the U.S. and key E.U. states pioneered the tactic just used by Lukashenko. They did so as part of a failed scheme to detain and arrest the NSA whistleblower Edward Snowden. That incident at the time caused global shock and outrage precisely because, eight years ago, it was truly an unprecedented assault on the values and conventions they are now invoking to condemn Belarus. In July of that year, the democratically elected President of Bolivia, Evo Morales, had traveled to Russia for a routine international conference attended by countries which export natural gas. At the time of Morales’ trip, Edward Snowden was in the middle of a bizarre five-week ordeal where he was stranded in the international transit zone of Sheremetyevo Airport in Moscow, unable to board a flight to leave Russia or exit the airport to enter Russia.
On June 23, Hong Kong officials rejected a demand from the U.S. Government that they arrest Snowden and hand him over to the U.S. Hong Kong was the city Snowden chose to meet the two journalists he had selected (one of whom was me) because of what he regarded as the city’s noble history of fighting against repression and for independence and free expression. When announcing their refusal to hand over Snowden, Hong Kong officials issued a remarkably defiant, even mocking statement explaining that Snowden had been permitted to leave Hong Kong “on his own accord.” That statement also accused the U.S. of having issued a legally improper and inaccurate extradition demand which they were duty-bound to reject, and then pointedly noted that the real crime requiring investigation was U.S. spying on the populations of the rest of the world.
Snowden thus left Hong Kong that day with the intent to fly to Moscow, then immediately board a flight to Cuba, and then proceed to his ultimate destination in a Latin American country — Bolivia or Ecuador — in order to seek asylum there. But even after then-President Barack Obama denied that the U.S. Government would be “wheeling and dealing” in order to get Snowden into U.S. custody — “I’m not going to be scrambling jets to get a 29-year-old hacker,” he dismissively claimed during a June press conference — the U.S. Government was, in reality, doing everything in its power to prevent Snowden from evading the clutches of the U.S. Government.
Led by then-Vice President Joe Biden, U.S. officials warned every country in both Europe and South America said to be considering shelter for Snowden of grave consequences should they offer asylum to the whistleblower. Threats to Havana caused the Cuban government to rescind its commitment of safe passage they had issued to Snowden’s lawyer. Under Biden’s pressure, Ecuador also reversed itself by proclaiming the safe passage document issued to Snowden was a mistake.
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The narrative of bitcoin energy use always seemed a bit warped.
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