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First Principles and Self-Controlled Opposition

By Emanuel E. Garcia, M.D. | NewZealandDoc | August 30, 2023

Being a psychiatrist certainly makes me no specialist in areas of immunology, cardiology, surgery or infectious disease. But having earned a doctorate in medicine I was provided an education in reasoning within this extraordinarily complex discipline from first principles. Therefore as an inquisitive physician throughout the covid operation, I could not help but be baffled by the response of institutional authorities.

Forgive me for repeating myself, but a ‘first principles’ approach would never have led to lockdowns, distancing, masks or the nefarious Jab. It would never have led to mandates or apartheid. And it would never have led to the promulgation of mRNA agents and the relentless push not only to inject all of humanity but, alas, all of the animal kingdom upon which humanity relies for food.

I repeat myself because with the whiff of yet another novel ‘variant’ restrictive measures are again in the news in America, whose so-called president has promised a yet more effective jab.

Effective at what, one may ask? At creating even more disastrous adverse effects and excess death? At degrading one’s natural immune system so as to render one more susceptible to infections and cancers?

Leaving aside the fact that I never believed a vaccine of any kind was necessary to manage the covid threat, for reasons I have laid out in many essays already, the description of the emergency-use instrument was proof enough for me that it would be a disaster. Flooding a body with millions upon millions of coronavirus spike protein antigens manufactured by the body itself, thanks to the integration of messenger RNA into cell machinery, did not seem like a very good idea — unless one wished to wreak havoc.

Even a psychiatrist like me could see that the potential for spike protein/antibody complexes in tremendous numbers could create autoimmune catastrophe via myriad mechanisms, and even a psychiatrist would suspect that somehow those pesky things would cross the blood-brain barrier despite assurances to the contrary. In short, I figured that they would go everywhere.

And so they have.

The greater looming question, a question that continues to vex me to this day, is why or how so many medical specialists — some of whom have now come to have changed their tune — initially insisted that the Jab would be advisable for the elderly and medically compromised, if not for all. And indeed I wonder how some of these specialists, prominent in the current opposition to the Jab, came themselves to have received it.

You see, to argue from another set of first principles — principles of psychological rationality — it simply made no sense then, nor does it make sense now. Nor does it make any conceivable sense that the astonishingly predominant majority of physicians could have touted the Jab, forgotten about informed consent and early treatment, and cheered the imprisonment of healthy people against all hitherto formulated pandemic guidelines.

That we have been betrayed by our institutional medical authorities, trans-nationally and intra-nationally — and here I am thinking not only of the infamously corrupt World Health Organisation and Federation of State Medical Boards but of entities such as the Medical Council of New Zealand and the American Board of Internal Medicine and many others — is no longer a surprise. We can see them for what they are, for the despicable agenda they have imposed, and for the scientific and ethical foundation they, by their actions, have destroyed.

That we have been betrayed by our governments also is no surprise, given their dismissal and oppression of the very citizenry from whom these governments are supposed to derive their power.

The fight against these powers is not easy, as we know; and as we also know these powers delight in confusing and dividing any concerted opposition, which they accomplish in many ways, so as to weaken us.

During ‘conventional’ wartime it is commonplace for adversaries to send out spies, to infiltrate each other, to play the game of double and even triple agents, and to mislead each other in every possible way. In this war — in this war of the Globalist Few against the Populist Many — the massive communications agency masquerading as ‘news’ and ‘trusted media sources’ has hammered away without pause. It’s an irregular and really unfair war, and a thoroughly unique one given its scale, even though the techniques themselves of artful deception and purposeful division and the combination of soft and hard force have been around forever.

That our enemy — the enemy of real science and human autonomy, the proponent of censorship and the persecution of dissent — will seek to control us is obvious. However, the notion of ‘controlled opposition’ is in vogue and proceeds too trippingly from the tongue. Strictly speaking it is only one of the various means and devices used to disrupt our clamoring.

I’ve never liked this designation because it can become another of those irrefutable assertions whenever a disagreement arises and can be made to cover so many scenarios that it loses usefulness. Surely there can be spies and traitors and infiltrators and the like, and there always will. That’s life.

I worry more about ‘self-controlled opposition’ — about people who need no higher official to pull their strings but who have an uncanny knack for knowing how to curry favor and when to keep from going ‘too far’.

A realist is compelled to acknowledge that within any group of people, on whatever side, personalities will arise whose fealty is more to themselves than to the common mission. These are the folks with the kind of pull that can bend a movement astray.

Vaccines have become a kind of black hole, sucking so much of our discursive energy into endless debate. I have learned over these past three and a half years that no vaccine can be trusted — just as no medication can be. It is sound and rational to demand to know about the ingredients and adjuvants of every vaccine, just as it is sound and rational to want to know how fluoxetine is supposed to work and how it might go wrong. But we are left with the choice to partake and receive, or not. A choice that is non-negotiable, no matter what our governments may say while brandishing their scepter of fear.

Which brings me back to first principles. When the rebellious crew of fifty-six Americans signed the Declaration of Independence, they made preeminently clear the principles of human autonomy, rights that were inborn rather then conferred. They were, naturally, creatures of their time, molded by its social and cultural and racial constraints. The first principles, however, that they espoused and enshrined, held with them the key to overcoming these constraints. It took a while for their reasoning to be extended to its logical end to include all men and women, regardless of color — but it got there thanks to the enunciation of these foundational principles.

Same for psychoanalysis. Whatever one thinks or knows or thinks he or she knows about Freud and analysis and the mores of fin de siècle Vienna, the principle of free association as a portal to the unconscious mind transcends the societal and cultural milieu of the age in which it was discovered.

As we fight this fight of our lives the surest sign of corruption within our midst is whether our leaders adhere to or stray from principle.

So, going forward, if I start hearing about a better mRNA vaccine or an improved method of masking or a friendlier way to limit our freedom to assemble; if I start to read about how the harsh measures imposed and the rationale for a lightning-quick jab had some merit, all in the name of the greater good of course, I’ll know whom I’m up against.

September 2, 2023 Posted by | Corruption, Deception, Science and Pseudo-Science | , , | Leave a comment

Ex-Italian PM: France Likely Downed Passenger Plane Trying to Kill Libya’s Gaddafi

© AP Photo / Saris
Sputnik – 02.09.2023

ROME – Former Italian Prime Minister Giuliano Amato has alleged that France and its US allies were likely responsible for the mysterious passenger plane crash off Sicily in June 1980, and that the incident was the result of a plot to assassinate late Libyan leader Muammar Gaddafi.

“The most credible version is about the responsibility of the French Air Force with the complicity of the Americans and those who participated in the air war over our skies on the evening of June 27,” Amato said in an interview with Italian newspaper la Repubblica on Saturday, recounting the June 27, 1980 crash of Itavia Flight 870, in which all 81 passengers and crew onboard were killed.

“A plan had been launched to hit the plane on which Gaddafi was flying,” Amato said, referring to reports of a dogfight taking place in the area between French and Libyan jets on the day the Italian passenger plane went down, and rumors that Gaddafi was on board one of the Libyan Air Force MiG jets.

The plan was to “simulate NATO drills involving many aircraft” during which a missile would have been fired – passed off as an accident – at the plane carrying Gaddafi, Amato said. However, Gaddafi got a warning from then-Italian Prime Minister Bettino Craxi, Amato’s former rival, and never boarded the jet, with the French missile allegedly intended for him ending up hitting the Itavia plane instead.

The Itavia McDonnell Douglas DC-9 passenger jet crashed into the Tyrrhenian Sea off the western Italian coast, between the islands of Ponza and Ustica en route from Bologna to Palermo.

In 2015, the Palermo Court of Appeal ruled that the crash was caused by a missile hitting the DC-9, and that the missile was fired by another aircraft that crossed the passenger plane’s route. The court ruled out previously claimed versions about a bomb being planted on board the civilian airliner.

In his interview on Saturday, Amato said the Elysee should admit its responsibility, so that it can “wash away the shame that weighs down on Paris.”

“After forty years, the innocent victims [of the crash] have not received justice. Why continue to hide the truth? The time has come to shed light on this terrible state secret. [French President Emmanuel] Macron could do it. And NATO could do it,” he said.

France and its US allies have long denied any involvement in Itavia Flight 870’s crash.

Commenting on Amato’s allegations, Italian Prime Minister Giorgia Meloni called on the politician to disclose any materials he may have related to the incident.

“Taking into account that the materials concerning the DC-9 tragedy are not classified, and that the judicial authorities and parliamentary commissions have done a lot of work over decades, I ask Amato to understand whether, in addition to his conclusions, he has other elements that allow him to review the decisions of the judiciary and the parliament, and possibly to make them available, so that the government can take all possible and consistent steps,” Meloni was quoted as saying in a statement released by her office.

September 2, 2023 Posted by | Deception, Timeless or most popular, War Crimes | , , | Leave a comment

NEW MASK STUDY SUPPORTING THEIR USE DEEPLY FLAWED

The Highwire with Del Bigtree | August 31, 2023

HEALTH HEADS KNEW COVID SHOT WASN’T ‘THE WAY OUT’

The Highwire with Del Bigtree | August 31, 2023

September 1, 2023 Posted by | Deception, Science and Pseudo-Science | | Leave a comment

Indonesia rubbishes Pentagon’s ‘joint statement’ on China and Russia

RT | September 1, 2023

Indonesia’s military chief has denied issuing any shared statements with his US counterpart during a visit to Washington last week, after the Pentagon published a “joint” press release attributed to Jakarta which criticized Moscow and Beijing.

Speaking to reporters on Thursday, Defense Minister Prabowo Subianto said the US statement does not reflect his country’s positions, stating that Indonesia seeks friendly relations with both Russia and China.

“There is no joint statement and no press conference. What is important for me to underline is that our relationship with China is very good. We respect each other, we already have mutual understanding. I conveyed that in the US,” he said, adding “We are close friends with China, we respect America, and we seek friendship with Russia.”

The official went on to announce plans to visit Beijing and Moscow in the coming months, voicing hopes that Jakarta could serve as a “bridge” between rival states.

The Pentagon missive, published on August 24 was titled ‘United States DoD and Indonesia MoD Joint Press Statement’ and took on a different tone. It claimed that both the US and Indonesia “shared the view that the People’s Republic of China’s (PRC) expansive maritime claims in the South China Sea are inconsistent with international law.” It also went on to “jointly” condemn Moscow’s actions in Ukraine, demanding a “complete and unconditional withdrawal” of Russian forces.

Though Indonesia’s Defense Ministry noted Subianto’s meetings with Pentagon head Lloyd Austin, it made no mention of any joint statement with Washington, and offered no comments about Russia or China.

Beijing was quick to jump on the American statement, with China’s embassy in Jakarta claiming the remarks had not been approved by Indonesian officials beforehand.

“We’re informed by the Indonesian side that what the US side described is not true. In fact, no such content can be found in the press release by the Indonesian side at the same meeting,” the embassy told reporters last weekend, slamming US efforts to “to sow discord and stir up trouble.”

During Subianto’s trip to the US, the two countries agreed to boost military cooperation, including joint war games and additional US weapons sales. The Pentagon further said Washington would help Jakarta’s military modernization drive, proposing “fighter aircraft upgrades, new multi-role fighter aircraft, and additional fixed and rotary wing transport aircraft,” among other gear.

Highlighting the growing military ties, Indonesian officials announced a deal to purchase 24 Sikorsky S-70M Black Hawk transport helicopters from US arms giant Lockheed Martin last week, soon after signing a major contract with Boeing for two-dozen F-15 fighter jets. Jakarta is working to revamp its air fleet, which currently operates systems from several different countries, including both US- and Russian-made fighter jets.

September 1, 2023 Posted by | Deception | , , , | Leave a comment

The climate scaremongers: Playing fast and loose with the facts

By Paul Homewood | TCW Defending Freedom | September 1, 2023

Climate alarmists love summer. It gives them an opportunity to exploit every heatwave, wildfire and hurricane. It is much harder to scare people in winter, when snow is supposed to be a thing of the past, and who doesn’t welcome a nice spring day or Indian summer?

So here are some of the silly scare stories which have appeared in the few weeks while we’ve been away.

1 Wildfires in Portugal

THE BBC went into full alarmist mode after some fires during a bit of hot weather in Portugal early last month. They reported: ‘Firefighters in Portugal are battling to contain wildfires engulfing thousands of hectares amid soaring temperatures. Around 800 personnel attended a fire near the southern town of Odemira overnight on Monday, with more than 1,400 people having to evacuate. At least nine firefighters have been injured tackling the fires. Temperatures in excess of 40C (104F) are expected to hit much of the Iberian peninsula this week.’

The BBC would like you to believe that hot weather is somehow unusual in Spain and Portugal! And as usual they provide no context at all. The big fire near Odemira burned 6,700 hectares (16,500 acres) but this is a tiny figure compared with the annual wildfire area in Portugal each year. And the data clearly shows there is no upward trend.

https://notalotofpeopleknowthat.wordpress.com/2023/08/09/shock-news-its-hot-in-portugal/

As for temperatures of 40C, what is so unusual about that? Temperatures of 39C in Cadiz are certainly not unheard of:

2 Wildfires in Hawaii

THE media quickly tried to link the wildfires on the Hawaiian island of Maui to global warming, with the BBC blaming a ‘dry summer’. The Guardian went one step further saying the fires were made worse by the climate crisis.

Summers in Maui are always dry. But as local experts have been warning for years, the intensity and rapid spread of this fire was the direct result of the spread of savanna-type grasslands in the last couple of decades.

Clay Trauernicht, a professor of natural resources and environmental management at the University of Hawaii, said it would be misleading simply to blame weather and climate for the blazes. Millions of acres of  Hawaii was cleared for plantation agriculture in the early 20th century, principally pineapple and sugar cane. Plantations were by and large fairly resistant to fire. However since 1980 they have shut one by one because of economic pressures, and now there are barely any left. In their place have come uncontrolled invasive species of savanna plants, such as Guinea grass which grows rapidly in the wet winters to a height of 10ft. In summer, these grasses quickly dry out, creating a tinderbox. All it needs is a spark and a strong wind to spread it, and the inevitable disaster will follow, just as it did last month.

Local fire and agricultural experts issued this very warning in a 2014 report, and recommended that the grasslands be properly managed and fire breaks be constructed. The authorities did nothing.

I doubt if you will read any of this in the Guardian.

3 The heatwave that never was

CAN the Met Office become an even bigger laughing stock than they are already?

On Wednesday August 16, they and the clowns at the UK Health Security Agency (UKHSA) announced a Yellow Heat Alert for most of England, saying that temperatures would peak at 28C (82F) on Friday the 18th. This in itself was absurd as 28C is hardly life-threatening!

Friday arrived, and most of us were trying to keep warm under grey skies and rain. If you were lucky enough to find a bit of sunshine, you might have got temperatures of 23C.

How can the Met Office have got it so wrong? Maybe in future they might try getting their forecasts right instead of spending their time pumping out global warming propaganda.

4 The storm that never was

ON THE same day that the Met Office announced the Yellow Heat Alert, they also issued a Yellow Warning for Storm Betty, as the Irish Met Office were to name it, which was due to hit us on the day on Saturday August 19.

According to the Met Office forecast on Friday morning, we could expect up to 80mm (3in) of rain and winds in excess of 70mph in exposed places, and 50mph more widely, particularly in West Wales which would see the strongest winds.

The reality was much more mundane. Ballypatrick in the hills of Northern Ireland saw the most rain, 36mm (1.4in), and the extremes in England and Scotland were much less. As for winds, the Met Office managed to find a handful of extremely exposed sites. Capel Curig, for instance, at an altitude of 216m (708ft) in the middle of Snowdonia, recorded 66mph.

Down in the real world it was no more than a breezy day. Even on the West Wales coast, which was supposed to be worst affected, gusts reached only about 20mph, with sustained winds of about 10mph. According to the Beaufort Scale, that would be described as a ‘gentle breeze’.

But Gentle Breeze Betty does not have quite the same ring about it!

5 It does rain in Southern California

TROPICAL storms rarely hit California, but that does not mean they never do. The reason has nothing to do with climate, it is simply that Eastern Pacific hurricanes usually head west, away from the coast.

Last week, Hurricane Hilary headed north instead, and made landfall in California as a weaker tropical storm. Naturally the BBC went into full alarmist mode, blaming it on climate change in an article full of misinformation. They claimed that rainfall records had been broken across the state and in particular in Palm Springs, though why one solitary town should be of any consequence is a mystery to me.

To push home their message, they said that Los Angeles was in ‘recovery mode’ after 2.48 inches of rain, a record for August apparently.

In reality, Hilary was no wetter than other tropical storms to hit California, and 2in of rain in a day is not unusual at all in Los Angeles:

As for Palm Springs, even that record claim does not stand up to scrutiny, since it was wetter in 1922.

The September 1939 tropical storm, El Cordonazo, followed the same path as Hilary, and dropped twice as much rain on Los Angeles as Hilary, as well as larger amounts elsewhere. Hurricane Kathleen in 1976 is generally accepted as by far the wettest to hit California, with the 14.76 inches that fell on Mount San Gorgonia in a day still the official state record. Kathleen was described as a 1-in-160-year event, with hundreds of homes damaged and parts of California declared a disaster area. The highest rainfall recorded from Hilary was 11.74 inches, and the damage was considerably less than in 1976.

So once again we find that the BBC is playing fast and loose with the facts so that it can promote its political agenda. The same applies to the MSM and the Met Office.

September 1, 2023 Posted by | Deception, Fake News, Mainstream Media, Warmongering, Science and Pseudo-Science | , , | Leave a comment

“You Don’t Listen to the Press . . . I’m Telling You”: Post Columnist Strikes Out at Those Questioning Prior False Claims

By Jonathan Turley | September 1, 2023

I recently wrote how the Washington Post issued a statement that declared that the newspaper was “standing by” columnist Philip Bump on his proven false claims on subjects ranging from Lafayette Park to Russian collusion. Bump’s prior claims have not only been conclusively shown to be false but other major media outlets have now rejected those claims. However, the Post claimed this week that they are in fact true in response to one of my earlier columns.

Now, Miranda Devine at the New York Post has written about a meltdown by Bump in a podcast interview with Noam Dworman, owner of New York’s own Comedy Cellar. Dworman had asked Bump to explain some of his claims and Bump offered one of the most vivid examples of the new media and it is chilling. After declaring that “I’m gonna lose my mind,” he stormed out of the interview after refusing to address the contradictions and dubious claims in his prior columns.

Dworman’s podcast interview stands as one of the most revealing and vivid examples of how the media has changed in the age of rage.  Bump moves quickly from the conversational to crazed when simply asked about the basis for his claims in the Washington Post.

Dworman was asking about the mounting evidence and contradictions in the Biden corruption scandal. Some of us have said that there is evidence of obvious corruption and influence peddling, but more investigation is needed to establish any basis for impeachment or criminal charges involving President Biden.  Bump, however, will have none of it. The Post writer (who demanded investigations of a wide array of Republicans on false stories with little evidence) is vehement that there is nothing to see here . . . and the public just has to take his word for it.

Dworman remains polite and pushes Bump to simply engage him in explaining some of the countervailing evidence. Bump responds “I just I’m gonna lose my mind. I’m gonna lose my mind.”

As the interview shuts down, Dworman asks “is there nothing we can talk about … half the country believes this stuff.”

Bump: “I know, because half the country doesn’t actually dig into the issues.”

Dworman: “Here’s your chance to disabuse people. They don’t read the Washington Post.”

Bump will have nothing of it as Dworman continues to try to get him to explain his controversial writings: “There’s just no point, because all you want to do is you want to have me here as the putative expert so that you can present me with things that have been debunked multiple times that I’ve written about.”

Dworman: “What’s been debunked?”

Bump: “These, these claims. I’ve written about this, this argument about his dad calling him. I’ve written about this. Did you read what I wrote?”

Dworman: “It’s not debunked. Neither of us were there.”

Bump: “Well, I debunked it in the standpoint that I’ve already addressed this and presented the counterarguments to it.”

Of course, Bump has been repeatedly shown to have pushed false claims and then refused to admit to his errors. Moreover, he has repeatedly been criticized for not honestly presenting the counterarguments.

Dworman makes another valiant effort: “I have two issues here. One is Joe Biden’s behavior and one is the issue of the press. The press actually bothers me more than Joe Biden.”

Bump, however, has all but left the building: “Because you don’t listen to the press. I’m sitting here and I’m telling you, you’re wrong about these things, and you don’t listen, and you continue to insist upon things that are, you know, parsing of language. And it’s just, it’s this is why I keep saying it’s silly.” He then says that he is leaving.

Dworman responded “Well, it’s a shame because this is a good conversation.”

Bump: “It’s not a good conversation, because you refuse to listen to what I’m saying to you. You asked me on to present evidence. I keep telling you.”

However, what he “keeps telling” Dworman and the public is to just accept his conclusions and not question his support and analysis.

Bump then walks out with a statement that captures perfectly the new media. He first attacks independent journalist Matt Taibbi and says that he has “an agenda.”

Dworman delivers a haymaker in response and states “You have no agenda.”

That is when Bump delivers his exit line that foreshadowed the Post statement on my column: “I do have an agenda … My agenda is to do my best to try and present accurate information to the public. And I have an institution behind me to hold me to account when I don’t do that, which I think is an important consideration.”

Indeed, the Post would then stand entirely behind Bump and claim that all of his false statements were true.  Even when other media have acknowledged that these claims were false, the Post insists that they remain true. Thus, the Post is now saying that the following are true despite findings by inspector generals and special counsels to the contrary: (1) Bill Barr did order the clearing of Lafayette Park for the Trump photo op, (2) Barr also lied when he denied the use of tear gas by federal personnel in Lafayette Park, (3) there was never any spying on the Trump campaign by the FBI, (4) Hunter Biden’s laptop was seeded with Russian disinformation, and (5) the Clinton campaign was not behind false Russian collusion claims. It is all now deemed true by the Post. It appears that, if “Democracy dies in darkness,” journalism more often dies in the light of day.

After all, the problem is not that they are false but that people just “don’t listen to the press. I’m sitting here and I’m telling you, you’re wrong about these things, and you don’t listen.”

September 1, 2023 Posted by | Deception, Fake News, Mainstream Media, Warmongering, Russophobia | , , | Leave a comment

How Fauci pulled the Moderna vaccine rabbit out of the hat

By Paula Jardine  | TCW Defending Freedom | August 30, 2023

In the new era of biosecurity totalitarianism when authorities actively seek to silence even the most qualified dissenting voices, perhaps nothing could be more corrosive to public confidence than finding that a leading research institute participated in a deliberate fraud. The scientific misconduct in question is the intentional selection of an inappropriate animal model for a pre-clinical study and its subsequent concealment. Intentional scientific misconduct for financial gain is fraud.The organisation in question is the US National Institutes of Health (NIH), the largest public funder of biomedical and behavioural research in the world, which describes itself as ‘the driving force behind decades of advances that improve health, revolutionize science, and serve society more broadly’. In this case, the interests served were the NIH’s own finances and those of a private company, Moderna.

The NIH was implicated by Stephane Bancel, CEO of Moderna, in an April 1, 2020 webcast hosted by MIT Sloan Business School Finance Professor Andrew Lo and co-hosted by the Laboratory for Financial Engineering. Bancel’s presentation, ‘Accelerating mRNA medicines to patients’, was about the company’s Covid-19 vaccine candidate mRNA-1273 developed jointly over the course of a pre-Davos January 2020 weekend with the NIH’s National Institute for Allergy and Infectious Disease (NIAID), led by Dr Anthony Fauci. Investor interest in the company and its vaccine was high. Moderna was leading the race for a Covid-19 vaccine with the NIH not long having announced that it had dosed the first human volunteer with mRNA-1273 in a Phase 1 clinical trial expected to run for six weeks.

An excited Bancel said, ‘What I want to share with you is just one set of data, but I think it is important. It is data that we published in our S-3 in February. This is the pre-clinical data on a related coronavirus MERS, the Middle East Respiratory Syndrome, that many of you will recall happened in the Middle East, in Saudi, a few years ago and a few years later again in South Korea. So what you see here is a rabbit model.’

Bancel showed his audience graphs of data from a pre-clinical study conducted on rabbits and concluded: ‘We are very excited to see this data that was realised with the NIH, with the team of Dr Tony Fauci.’

One of the graphs showed antibody levels over time in a placebo group injected with saline and in single and double dose vaccine groups. But the antibody levels induced by the vaccine doses should have been compared with the levels of antibodies produced by exposure to the MERS virus itself, as a vaccine response must be shown to be superior to antibody levels induced by natural infection to be beneficial. Alongside was a second graph showing viral loads in the nose, throat and lungs following a challenge test in which the animals were exposed to ‘much higher doses of virus’ than during a natural infection. A caption on the slide claimed ‘We observed an induction of neutralising antibodies (my italics) that reduced viral load in the nose, throat and lungs of vaccinated animals’.

The rabbit study was not intended to fool drug regulators, who require an explanation of the relevance of the chosen animal model to the human disease the vaccine is meant to be protecting against. Customarily, before drug regulators permit clinical trials to begin with human volunteers, the efficacy of the candidate vaccine in preventing symptomatic clinical disease and/or pathologies associated with the disease must be demonstrated in a suitable animal model. The induction of antibodies is evidence of immunogenicity but in and of itself is not evidence of efficacy. Antibodies can be either neutralising or non-neutralising, the latter meaning that they fail to prevent reinfection following exposure to the targeted virus.

The choice of animal model for pre-clinical trials is an important one and consequently animal models must be validated. The scientific evidence that rabbits are an unsuitable model for testing the efficacy of a MERS vaccine had been in the public domain for years. In July 2019, the Coalition for Epidemic Preparedness Innovations (CEPI) hosted a workshop and subsequently commissioned IAVI (International Aids Vaccine Initiative) to prepare a report, ‘MERS-CoV standards, assays and animal models vaccine development landscape analysis’, which was funded by the NIAID, NIH, and the US Department of Health and Human Services (HHS). So far as rabbits are concerned it concluded: ‘Despite the fact that rabbits shed MERS-CoV from their URT [upper respiratory tract], it appears that the New Zealand white rabbit model is neither suitable to study MERS-CoV transmission, nor is the model appropriate for studying clinical disease progression, given that rabbits remained asymptomatic after MERS-CoV inoculation.’

The CEPI report states: ‘Since concerns over SARS-related pathology led to a US Food and Drug Administration (FDA) clinical hold on vaccine studies, investigation of MERS-CoV vaccine candidates to induce virus-enhancing antibodies and harmful immune response in animal models could be informative before human clinical trials are initiated.’

The FDA ‘hold’ followed the October 2014 gain of function research moratorium on SARs, MERS and influenza ordered by the US government. However some research on MERS continued. As some people were believed to have asymptomatic MERS infections and rabbits were known to be asymptomatic when infected with it, researchers from the NIAID studied the phenomenon in rabbits. The NIH declared the experiments ‘were determined by the NIH to be urgently necessary to protect the public health or national security and as such, were exempted from the US Government Research Funding Pause on Selected Gain-of-Function Research Involving Influenza, MERS, and SARS viruses.’

The results of this asymptomatic study were published in 2017.  The findings were not positive: ‘The rabbits developed antibodies against viral proteins that lacked neutralizing activity and the animals were not protected from reinfection (my emphasis).’ Further, the study found that even without an increase in viral RNA titers, reinfection resulted in increased inflammation of the lungs. The researchers warned: ‘Our data from the rabbit model suggests that people exposed to MERS-CoV who fail to develop a neutralizing antibody response, or persons whose neutralizing antibody titers have waned, may be at risk for severe lung disease on re-exposure to MERS-CoV.’

Bancel told the webinar audience that mRNA mimics natural infection without introducing the actual virus. But if exposure to the virus itself does not produce antibodies that protect against reinfection, there is no mechanism by which artificially stimulated antibodies can, thus rendering the company’s specific claim that the MERS vaccine induced ‘neutralizing antibodies’ untrue. The company repeated the claim in the S-3 referred to by Bancel, which was a $500 million supplementary stock offer made in February 2020, where investors were told: ‘We have demonstrated the ability to induce neutralizing antibodies that confer protection against viral challenge with a related coronavirus, MERS.’

Bancel said that Fauci’s team at NIAID helped Moderna realise the data, raising the question of why NIAID would accept the use of a model their own researchers who conducted the 2017 study knew to be unsuitable?

The week before the Phase 1 human clinical trial started in March 2020, STAT News reported on Moderna’s pre-clinical animal studies. None of the interviewees mentioned the MERS rabbit study that Moderna presented to investors and the US Patent Office the previous month. STAT News reported that they had been told by NIAID by email that ‘Virologists at NIAID tried the new vaccine [mRNA-1273] on run-of-the-mill lab mice, on the same day that the [phase 1] trial began enrolling participants’. They quoted Dr Barney Graham, the now retired Director of the NIAID Vaccine Research Centre, as saying that those mice showed the same sort of immune response generated by a similar mRNA vaccine against MERS, another coronavirus. ‘That level of immune response was sufficient to protect mice from MERS CoV infection,’ he wrote. Graham also said that mice susceptible to SARS-CoV2 ‘are being bred so that the colony can be enlarged’ adding that they ‘will be available for experiments within the next few weeks’.

Humanised mice are a validated study model for MERS, whereas rabbits are not, so if data from a mouse study of the mRNA-MERS vaccine was available, as Graham claimed, why wasn’t it used in Moderna’s February prospectus and the patent application?

Under the Research Collaboration Agreement between Moderna and NIAID, which has an effective date of July 19, 2019, NIAID was to conduct immunogenicity studies on Moderna’s mRNA-MERS vaccine in animals. During 2020, Dr Kizzmekia Corbett, the NIAID researcher assigned to run these studies for Moderna’s Covid-19 vaccine mRNA-1273, wrote two papers: a June 11, 2020 preprint article entitled ‘SARS-CoV2 mRNA vaccine development enabled by prototype pathogen approach’ and a second peer reviewed paper published in the journal Nature on August 5, 2020 entitled ‘SARS-CoV-2 mRNA Vaccine Development Enabled by Prototype Pathogen Preparedness’. In addition to mice studies on mRNA-1273, both papers cite the mRNA-MERS mouse study that Graham told STAT News about. Neither mentions an mRNA-MERS rabbit study. Oddly, neither is the mRNA-MERS vaccine’s alpha-numeric identifier given.

Heavily redacted copies of Moderna’s contracts with NIAID were released following a freedom of information application by AXIOS News. On December 17, 2019, Moderna signed a material transfer agreement (MTA) transferring ‘mRNA coronavirus vaccine candidates developed and jointly owned by NIAID and Moderna’ to Dr Ralph Baric at the University of North Carolina Chapel Hill (UNC-CH), directing him to perform animal challenge studies. The research programme is redacted. More suspiciously, so is the animal model stipulated in paragraph 3. Dr Baric did not respond when he was asked by me if he was commissioned to run the mRNA-MERS rabbit study.

Dr Baric is widely regarded as the world’s leading coronavirus researcher. He was a member of the World Health Organization working group on animal models to accelerate the development of Covid-19 vaccines and therapeutics. So too was Dr Graham who signed the MTA on behalf of NIAID. Given their expertise, the selection of a suitable animal model should have been a straightforward matter rather than a contentious one requiring concealment. One possible explanation for why experts would choose an inappropriate model is that they were in a hurry and suitable mice were not available. As per a 2015 paper in Virology, the first transgenic mice for MERS research were bred by Dr Agarwal at the University of Texas. Laboratory mice specially bred such as those developed by Dr Baric for his research into the original SARS are not susceptible to MERS. Baric certainly has the expertise to breed his own, given sufficient time. In 2020, he filed an invention report with UNC-CH (UNC ref 18752) for a mouse adapted model to test SARS-CoV-2 countermeasures.

On December 16, 2019, the day before Moderna signed the Baric MTA for the jointly owned Moderna/NIAID mRNA coronavirus vaccines, the company signed an amendment to the July 2019 NIAID research collaboration agreement. This amendment was countersigned by Vincent Feliccia, the branch chief of NIAID Technology Transfer and Intellectual Property Office, on January 13, 2020, the day the design of Moderna’s SARS-CoV-2 vaccine was finalised.

Intentional scientific misconduct for financial gain is fraud. In addition to publishing the mRNA-MERS rabbit data in its supplementary stock offer, Moderna used it to apply for a patent for an mRNA-betacoronavirus vaccine on February 28, 2020. The same patent covers Spikevax, its Covid-19 vaccine. The US Patent Office is notoriously poor at detecting scientific fraud in patent applications even when it is in the public domain. In 2014 it astonishingly issued a patent to Dr Hwang Woo-suk for a technique to clone human embryos although the associated journal paper had been retracted in 2005 due to the data having been faked. Unlike drug regulators, the Patent Office apparently does not require the use of validated animal models, or a justification for the selection of a given model.

As was widely reported in 2021, Moderna and NIAID became embroiled in a dispute over the NIAID’s ownership interest in mRNA-1273. The company omitted to include Dr Kizzmekia Corbett, Dr Barney Graham and his boss, Dr John Mascola, when it filed for its patent. An NIH spokesperson told CBS news: ‘Omitting NIH inventors from the principal patent application deprives NIH of a co-ownership interest in that application and the patent that will eventually issue from it.’

As of the end of February 2023, Moderna is reported to have earned $36billion from Spikevax. Despite the ongoing patent dispute with NIAID, following negotiations in December 2022 the company gave NIH a $400 million ‘catch-up royalty payment’.

Under the provisions of the Bayh-Dole Act, US government researchers are also entitled to receive up to $150,000 in royalties annually if their inventions are commercialised. Meanwhile, despite Bancel’s initial enthusiasm for sharing the mRNA-MERS rabbit data, it soon disappeared. Perhaps that’s because it’s hard to see how their indemnity shield under the US Public Readiness and Emergency Preparedness (PREP) Act stretches that far.

August 30, 2023 Posted by | Corruption, Deception, Science and Pseudo-Science, Timeless or most popular | , , | Leave a comment

The FDA Can Say (and Do) Anything It Wants

For example, they can’t be sued for providing false or dishonest information

By John Droz Jr. | Critically Thinking About Select Societal Issues | August 10, 2023

This is an extraordinarily important commentary!

The gist of a current court case that you’ve likely never heard of, is that three heroic doctors are suing the FDA about the loss of their jobs, about their careers being derailed, about the loss of their reputation — all because their professional, scientific opinion as to what was in the best interest of their patients, was different than the political agenda of the FDA. (Here is a bit of background.)

What is at stake here could not be more significant, and it applies across the board to EVERY federal agency. The question is: do federal agencies have the unsupervised right to replace Science with political science? Put another way: can they act dishonestly, incompetently, etc. with essentially no meaningful consequences?

Here is the doctors’ Complaint. Although it was filed a year ago, it is now being appealed this week — and some fascinating audio clips have emerged. There are three judges on a panel, asking the attorney representing the FDA some probing questions.

Five of these short audio clips (3-5 minutes each) are posted here. (The recording of the full proceeding is here.)

IMO some of the key takeaway revelations (so far) are:

1 – The FDA seems to claim that their published warnings are little more than offhand observations. For example, their slamming of Ivermectin was evidently just casual commentary (what the FDA calls “informational”).

Note the title here, on this FDA page which is STILL up! It says “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19”.

Note 1: This is a deceptive headline because that article is mostly saying: a) citizens should not self-medicate, and b) using any veterinary medications can be dangerous. Both of these are legitimate concerns. So, if the FDA was honestly trying to benefit the public their heading should be: “Why You Should Not Self-Medicate Using Veterinary-Grade Ivermectin to Treat or Prevent COVID-19”. BIG DIFFERENCE!

Note 2: This FDA page has changed quite a bit over time. Here is the 2021 version.

Note 3: The current page makes outright false statements like: “Ivermectin has not been shown to be safe or effective for these indications.” I’m one of the few people who has taken the time to put together a spreadsheet of ALL the studies on ALL the major COVID early treatment therapies: see it here.

There have now been 99 Ivermectin scientific studies, and the overall early treatment effectiveness is 62%. IVM’s extensive safety record is extraordinary, with adverse effects (e.g., see here) in the ballpark of only one in a million usages!

Now, also on my spreadsheet, compare what the FDA has approved for early treatment of COVID-19 therapy: Paxlovid = 32% effective with these adverse safety issues, and Molnupiravir = 16% effective with these problematic safety issues!

Despite these LARGE benefits of Ivermectin in effectiveness and safety, the FDA continues to say that “Ivermectin has not been shown to be safe or effective” for early treatment of COVID-19. This is stunningly inaccurate.

Note 4: Even though the FDA now has access to 99 Ivermectin studies, their statement against Ivermectin is stronger now than when the page originally appeared in 2021! IMO this is what happens when a federal agency feels that there is no meaningful oversight, so effectively they can say anything they want.

2 – The FDA says that Courts have no business in reviewing anything they say or do!

Considering the above facts in #1, it’s obvious why this would be their self-serving position. Listen carefully to the second short audio clip, where the FDA’s attorney appears to say that the FDA’s communication to the public can be knowingly false, dishonest, etc. with no oversight or consequences — even when deaths result!

Regretfully, to date, the courts have played along with this game of charades. For example, the Chevron case is frequently cited by non-aggressive attorneys to say that courts will stay out of determining whether FDA processes, documents, and claims are legal, accurate, honest, warranted, etc.

However, that is an oversimplified opinion. Even the Chevron case states that the FDA’s actions must be “reasonable” — but that is rarely argued. BTW, the case we are discussing here would never have been filed if the doctors’ attorneys bought into the bogus idea that federal agencies have unlimited deference. Kudos to them that they did not accept that absurd argument!

Maybe I’m overly optimistic, but based on the judges’ questions and comments in these clips, it seems to me that this case might eventually upend Chevron. That would be EXTRAORDINARILY beneficial for US citizens, as it would apply to all national policies: from immigration to education, energy to climate change, etc.

3 – The FDA asserts that the only recourse that US citizens have about even egregious errors and deceptions by the FDA is through the “political process.” Astounding!

4 – The FDA indicated that the “political process” means that citizens need to elect a competent and attentive President, whose responsibility it is to see that the FDA acts responsibly — or else. The flip side is that when we do not have such a President, all federal agencies have a four-year time period to wreak whatever political havoc that suits them — again, across the board, and without real consequences to the guilty parties.

5 – The FDA’s attorney implied that there would be no compensation given for inaccurate or knowingly false FDA statements — including those that lead to Americans unnecessarily dying — other than an FDA person may lose their job.

6 – Based on these select audio clips, the fact that hundreds of thousands of Americans likely died needlessly due to the FDA’s COVID actions and inactions (see here), was not fully addressed. Hopefully, this will be brought up in this trial.

7 – In clip #3, the FDA attorney makes the startling claim that the FDA has the authority to give citizens medical advice! How is that possible when they know nothing of the medical history of any American citizen? Further, once they assert that right, how is a conflict resolved between what the FDA says and what a citizen’s medical provider says? That is one of the major issues in this important case.

8 – In clip #4, the FDA attorney acknowledges that doctors have lost their jobs, etc. due to their scientific conclusions on such matters as Ivermectin, and their science-based actions that they believed were in the best interest of their patients. However, the FDA attorney then stated that no losses, etc. were due to anything the FDA did. (!)

……….

Note that a lot of the bad behavior with the FDA (and CDC) would be reduced if the Medical Establishment refused to play politics and instead supported real Science for the public. Regretfully, that has not happened and the COVID-19 fiasco exposed this ugly underbelly. See my Report on the COVID failings of the Medical Establishment.

In another Report, I compared the FDA’s approval process for Remdesivir to Ivermectin. This appears to show stunning incompetence at the FDA.

I have made this point before, but it’s worth repeating. The war we are engaged in is that powerful Left-wing forces (exterior and from within) are trying to take America down. One of their primary strategies to do this is to replace Science with political science. That is what this case is about, as the FDA is specifically arguing that they have the right to scrap Science and substitute political science — with impunity!

Draw your own conclusions, but to me, this case is like a Molotov cocktail thrown into the Federal Government bureaucracy. Astoundingly, all three branches of our government are complicit with this nonsense.

Some obvious questions that need to be answered and fixed are: 1) How did Congress give pharmaceutical companies such broad protections against self-serving unscientific actions? 2) How did the Executive branch allow agencies like the FDA to be run by parties that they are supposed to regulate? 3) How did our Judicial system allow bad actor agencies to arrange to have no real legal oversight?

Considering that these failings are applicable to multiple federal agencies, is there any question why such things as COVID policies (and energy, and climate, and education, and immigration, and elections, etc., etc.) are a disaster?

Hopefully, this lawsuit will crack open the door to fixing this horrific mess…

……….

PS — What needs to be done now :

1) Competent attorneys should file friend of the court briefs to support this nationally important case. Overturning the Chevron precedent would have extraordinarily positive benefits for almost ALL US citizens.

2) Competent federal legislators should introduce a “Save America” bill (aka Agency Oversight Act). This legislation will rein in ALL federal agencies, by providing timely and meaningful oversight (plus real penalties) to them all.

August 30, 2023 Posted by | Deception, Science and Pseudo-Science | , , , , | Leave a comment

Latest Biden coverup — 5,400 emails he sent under secret names

By James Bovard | New York Post | August 29, 2023

In Washington, conning the American people is always considered a victimless crime. The latest DC shellshocker is the National Archives blocking release of 5,000+ emails Vice President Joe Biden wrote using a pseudonym to shroud Biden family graft.

In ancient Rome, the consul Scipio was accused of abusing his power. He stood in front of the Senate, pulled out the written records of his reign and tore them to pieces. Scipio’s reputation was so impeccable that the audience cheered him, regardless of his destruction of evidence.

Bizarrely, this is the same template the liberal media use to whitewash President Biden. Americans don’t need to know the facts of how Biden has used his power because his intentions are good.

But the only reason his intentions appear good is because we don’t have the facts.

Consider the latest wacky revelations on the nom de crook. In response to a Freedom of Information Act request, the National Archives admitted there are 5,400 emails Biden apparently sent under fake names including robinware456@gmail.com, JRBWare@gmail.com and Robert.L.Peters@pci.gov.

A few of those emails have trickled out from other sources, revealing messages tied to Hunter Biden’s Ukraine hustle. But the Archives is refusing to reveal thousands of other messages despite disclosure demands from the House Oversight Committee.

Biden declared in 2019 that there was “an absolute wall” between Biden family foreign schemes and his own role as vice president. Apparently, the “absolute wall” only applied to the specific name “Joe Biden.”

Did Biden take a class in law school on Incognito Influence Peddling or what?

This is the second Biden scandal recently exposed. In 2018, Biden bragged to a Council on Foreign Relations audience that he threatened to withhold a billion dollars in foreign aid to Ukraine unless that government immediately fired its chief prosecutor in December 2015.

Biden claimed the prosecutor was corrupt, yet State Department and other documents released last week reveal that the Ukrainian prosecutor had Washington’s trust. But that prosecutor was closing in on Burisma, threatening the million dollars a year in payoffs pocketed by Hunter Biden.

If those documents had surfaced during the first Trump impeachment case in late 2019, Donald Trump’s behavior would have appeared less conniving and Biden would have looked more conniving. (Both of them would still have looked like hell.)

Two years after Biden finagled that firing to purify the US ally, Ukraine was ranked the most corrupt nation in Europe except for Russia.

Biden owes his 2020 presidential election victory to pervasive, perpetual federal coverups. The Hunter Biden laptop coverup was only the tip of the bureaucratic iceberg.

How many other Biden scandals are scattered like unexploded cluster bombs throughout federal filing cabinets inside the Beltway?

How many other FBI memos exist on potential Biden bribes that we have not heard about?

How many Treasury Department Suspicious Activity Reports on massive wire transfers from squirrely foreign entities to Biden Inc. have not surfaced?

Are there other IRS investigations that were squelched without a trace?

Federal secrecy and coverups switched more votes in 2020 than Trump’s antics in Georgia and elsewhere ever could have flipped. Biden’s yammering about how his election was “the will of the people” looks more deranged with each new exposé of his pre-election abuses.

Federal Judge Amy Berman Jackson declared in 2019, “If people don’t have the facts, democracy doesn’t work.” Why bother having a national election if the result merely reveals how many voters were hornswoggled by secrets the feds kept from them?

Politics has rarely been an honest business, but the combination of pervasive secrecy and perpetual deceit makes a mockery of every high-school civics-class lesson.

Will the National Archives go to the barricades to defend the privacy interest of Joe Biden’s imaginary friends? Will dogged investigators, congressional committees and whistleblowers obliterate the tattered remnants of Team Biden’s credibility? Will the liberal media cease invoking the president’s good intentions to expunge his crimes?

August 30, 2023 Posted by | Civil Liberties, Corruption, Deception, Full Spectrum Dominance | | Leave a comment

Contaminating Good Data With Bad

tonyheller | August 27, 2023

Temperatures in cities have been known for a long time to be much warmer than surrounding rural areas. Instead of eliminating the Urban Heat Island contaminated data, NASA and NOAA use it contaminate surrounding rural stations as well.

August 29, 2023 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, Video | , | Leave a comment

Pfizer drip feeds data from its pregnancy trial of covid-19 vaccine

Analysis of the data so far shows the trial was underpowered, poorly designed and incomplete

BY MARYANNE DEMASI, PHD | AUGUST 24, 2023

In January 2021, in the absence of any human data in pregnancy, the CDC stated on its website that mRNA vaccines were “unlikely to pose a specific risk for people who are pregnant.”

Former CDC director Rochelle Walensky backed it up with a full-throated endorsement of covid-19 vaccination in pregnancy.

“There is no bad time to get vaccinated,” said Walensky.

“Get vaccinated while you’re thinking about having a baby, while you’re pregnant with your baby or after you’ve delivered your baby,” she added.

Behind the scenes however, Pfizer was scrambling to conduct a clinical trial of its vaccine in pregnant women.

By February 2022, Pfizer revealed it still did “not yet have a complete data set.” Its statement read:

“The environment changed during 2021 and by September 2021, COVID-19 vaccines were recommended by applicable recommending bodies (e.g., ACIP in the U.S.) for pregnant women in all participating/planned countries, and as a result the enrollment rate declined significantly.”

This month, Pfizer finally posted some trial results on clinicaltrials.gov.

The data do not appear in a peer-reviewed journal or a pre-print, nor has it been submitted to the FDA for evaluation.

I spoke with experts who have analysed the data with a fine-tooth comb and made some alarming observations.

Trial design

Pfizer originally planned to recruit 4000 healthy women aged 18 or older who were 24 to 34 weeks pregnant. Half would be randomised to the vaccine and the other half to a saline placebo.

The efficacy and safety of the vaccine would be determined by assessing covid-19 cases, antibody responses, and adverse events.

Peculiarly, Pfizer planned to vaccinate all the mothers in the placebo group, one month after giving birth to their babies.

Retsef Levi, a professor at the Massachusetts Institute of Technology Sloan School of Management said that vaccinating mothers in the placebo group during the assessment period would introduce a new variable into the experiment and “corrupt” the data.

“We now know that mRNA from the vaccine is detected in the breast milk, so those babies born from mothers who were all vaccinated after giving birth, are also potentially exposed to mRNA through breastfeeding,” explained Levi.

“This corrupts the comparison of the two groups of babies because you don’t have a true control group anymore,” he added.

Sample size too small

Less than 10% of the originally planned 4000 study participants ended up in the trial.

“Only 348 women were recruited – 174 in each arm – meaning that the trial was never going to have the statistical power, particularly when analysing potential harms,” said Levi.

Notably, study protocols indicate that Pfizer was given the green light as early as May 2021 by drug regulators to scale back the trial and reduce the sample size.

“To me, the wording in the protocol suggests that the FDA or another regulator basically gave Pfizer permission to do less,” remarked Levi.

“It’s not surprising though. The vaccine had already been recommended for pregnant women and many have taken it, so there is no upside to completing a trial that may detect signals of potential harms. It can only create problems for them, right?” he added.

Given that pregnant women were being vaccinated with a product that had not undergone rigorous safety testing in pregnancy, the FDA was asked if and why it allowed Pfizer to scale back the trial.

The FDA replied, “As a general matter, FDA does not comment on interactions it may or may not be having with sponsors about their clinical trials.”

Angela Spelsberg, an epidemiologist and medical director at the Comprehensive Cancer Center Aachen in Germany agreed that the integrity of the study had been compromised.

“There are just not enough babies in this trial to detect rare or very rare adverse events. We learned from studies in animals that lipid nanoparticles in the vaccine can deposit in many organs including the ovaries, so we must be extremely cautious about the potential negative impacts of the vaccine on reproductive health,” said Spelsberg.

“The scientific community urgently needs access to the pregnancy study data on the patient level for transparency and independent scrutiny of vaccine safety and efficacy because regulatory oversight is failing,” she added.

Exclusion criteria

The small sample size may have been the result of the strict selection process.

Pfizer recruited participants with an impeccable pregnancy history, and most were in their third trimester (27-34 weeks gestation), a stage when the baby’s major development has already occurred.

“It appears that they cherry picked the mothers to get the best results,” said Levi. “We have no idea what impact this vaccine has on the early stages of development of an embryo or foetus, because all the women had advanced pregnancies when they were recruited.”

Spelsberg agreed.

“The first trimester is particularly vulnerable to adverse reproductive health outcomes,” she said.

“Based on only weak observational evidence, regulators have reassured the public that the vaccines are safe throughout pregnancy. However, we don’t have reliable evidence on the vaccine’s impact on miscarriages, malformation, foetal deaths, and maternal health risks because they excluded pregnant women from pivotal trials,” added Spelsberg.

Missing data

Levi also noticed that “only partial data” were published.

“It doesn’t include any important metrics such as covid infections or antibody levels and its says we must wait until July 2024 for those results. It’s disturbing to say the least,” said Levi.

Also missing from the dataset was a full account of birth outcomes. Of the 348 women in the trial, Pfizer only reported on the birth of 335 live babies.

Of the 13 pregnancies unaccounted for, Pfizer reported one foetal death (stillbirth) in the vaccine group and the outcome of the other 12 pregnancies remains unknown.

“This is unacceptable,” said Levi. “Failing to report the outcome of 12 pregnancies could mask a potentially concerning signal of the vaccine in pregnancy. What happened to the babies, did they all die? Were their mothers vaccinated or unvaccinated?”

Trial dropouts

Finally, there were quite a few babies that were lost to follow-up in the trial.

“Twenty-nine babies in the placebo arm didn’t get to the end of the 6-month surveillance period, versus 15 babies in the vaccine arm. That’s almost double. Again, this is concerning and requires a detailed and transparent explanation,” said Levi.

Overall, both Levi and Spelsberg say the delays and failure to disclose vital data are unacceptable.

“Pfizer took a year to publish the data. When they finally did, it is incomplete. And we are expected to wait until July 2024 for the next batch of results, while authorities continue to recommend the vaccine in pregnant women,” said Levi.

“We still don’t have solid scientific evidence whether this vaccine is safe for pregnant women and their babies,” said Spelsberg. “It’s a tragedy and a scandal that vaccine use has been recommended, even mandated to women before, during and after pregnancy.”

Questions were put to Pfizer, but the company did not respond by the deadline.

Moderna is also conducting a clinical trial of its mRNA vaccine in pregnancy, but no data are available.

August 28, 2023 Posted by | Deception, Science and Pseudo-Science, War Crimes | , , | Leave a comment

3M to pay billions to settle lawsuits over US military earplugs

RT | August 28, 2023

American multinational conglomerate 3M has agreed to pay more than $5.5 billion to settle hundreds of thousands of lawsuits, claiming that it supplied defective combat earplugs to the US military, people familiar with the deal told Bloomberg.

According to the agreement, the company will be paying the money out over a five-year period, the agency reported on Sunday. 3M’s board is yet to sign off on the settlement, it added.

When approached on the issue by Bloomberg, a representative of 3M said the company does not comment on rumors or speculation.

3M faces more than 300,000 lawsuits from US troops, consolidated in a multi-district litigation, claiming that the earplugs that the company’s subsidiary Aearo Technologies provided to the military between 2003 and 2015 were defective, and failed to protect their users from hearing loss and tinnitus.

Current and former servicemen alleged that the company knew its earplugs were faulty, but did not inform the military about the problem, while making no steps to fix the product.

The earplugs, designed to protect the hearing of troops during training and combat, were standard issue for US soldiers in Iraq and Afghanistan.

3M failed 10 out of 16 early trials over the plugs, and has been told to pay over $250 million in damages to more than a dozen plaintiffs.

Bloomberg noted that the reported settlement would allow the company to avoid a much larger liability, which it estimated at up to $9.5 billion.

“Sounds like 3M negotiated a pretty good deal for itself, given this litigation has been weighing on them for the better part of a decade,” University of Richmond law professor Carl Tobias told the agency.

3M had earlier sought bankruptcy for Aearo Technologies in an attempt to shield itself from the lawsuits over earplugs. However, this June, a judge ruled that the firm’s financial troubles were not harsh enough to initiate the procedure.

The same month, 3M announced that it had reached a $10.3 billion settlement with a host of US public water systems to resolve water pollution claims tied to so-called “forever chemicals” or per- and polyfluoroalkyl substances (PFAS) used in the company’s products.

August 28, 2023 Posted by | Deception, Environmentalism | | Leave a comment