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Brownstone Institute

Another Tacit Admission That COVID Mandates Were a Disastrous Mistake

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From the Brownstone Institute

BY Ian MillerIAN MILLER

Pandemic restrictions were an unmitigated failure, and the evidence base against the politicians and “experts” who imposed them and demanded compliance continues to grow.

And it raises some substantial questions about holding those responsible accountable for their actions. Especially as mask mandates return in certain parts of the country, with hints of more on the way.

Recently a new government report from the United Kingdom was released to little fanfare, which not-so-surprisingly mirrors the fanfare resulting from the release of new data from the CDC itself, showing how vaccine efficacy has fallen to zero.

Finally, Rochelle Walensky did acknowledge publicly that the vaccines couldn’t stop transmission. However it was already far too late to matter.

But all along the agency has strongly stated that the mRNA shots were effective at preventing hospitalizations. Or at least that the latest booster was effective, tacitly acknowledging that the original 2=dose series has lost whatever impact it once had.

What The Evidence Says About NPI’s

The UK’s Health Security Agency (HSA) recently posted a lengthy examination on the effectiveness of non-pharmaceutical interventions at preventing or slowing the spread of COVID-19 in the country.

And at the risk of revealing a spoiler alert, it’s not good news for the COVID extremists determined to bring mask mandates back.

The goal of the examination was laid out succinctly; the UK’s HSA intended to use primary studies on NPIs within the community to see how successful or unsuccessful they were at reducing COVID infections.

The purpose of this rapid mapping review was to identify and categorise primary studies that reported on the effectiveness of non-pharmaceutical interventions (NPIs) implemented in community settings to reduce the transmission of coronavirus (COVID-19) in the UK.

Streamlined systematic methods were used, including literature searches (using sources such as Medline, Embase, and medRxiv) and use of systematic reviews as sources to identify relevant primary studies.

Unsurprisingly, they found that the evidence base on COVID interventions was exceptionally weak.

In fact, roughly 67 percent of the identified evidence was essentially useless.. In fact two-thirds of the evidence identified was modeling.

Two-thirds of the evidence identified was based on modeling studies (100 out of 151 studies).

There was a lack of experimental studies (2 out of 151 studies) and individual-level observational studies (22 out of 151 studies). Apart from test and release strategies for which 2 randomised controlled trials (RCTs) were identified, the body of evidence available on effectiveness of NPIs in the UK provides weak evidence in terms of study design, as it is mainly based on modelling studies, ecological studies, mixed-methods studies and qualitative studies.

This is a key learning point for future pandemic preparedness: there is a need to strengthen evaluation of interventions and build this into the design and implementation of public health interventions and government policies from the start of any future pandemic or other public health emergency.

Modeling, as we know, is functionally useless, given that it’s hopelessly prone to bias, incorrect assumptions and the ideological needs of its creators.

The two paragraphs which followed are equally as important.

Low quality evidence is not something that should be relied upon for decision making purposes, yet that’s exactly what the UK, US and many other countries did. Fauci, the CDC, and others embraced modeling as fact at the beginning of the pandemic. They then repeatedly referenced shoddy, poor quality work because it confirmed their biases throughout its duration, with unsurprising results.

And this government report concurs; stating simply and devastatingly, “there is a lack of strong evidence on the effectiveness of NPIs to reduce COVID-19 transmission, and for many NPIs the scientific consensus shifted over the course of the pandemic.”

Of course the scientific consensus shifted over the course of the pandemic because, as we learned, it became politically expedient for it to shift.

As their paragraphs on the available evidence show, there was little solid, high-quality data showing that NPI’s were having a significant impact on the spread of the virus, a reality that had been predicted by decades of pandemic planning.

But the consensus shifted towards NPIs and away from something approaching Sweden’s strategy or the Great Barrington Declaration, simply because Fauci, the CDC, and other “experts” demanded it shift to suit their ideological aims.

The few high-quality studies on say, masking, that were conducted during the pandemic showed that there was no benefit from mask wearing at an individual or population level. And that is why the Cochrane review came to its now infamous conclusion.

Instead of acknowledging that they were relying on poor quality evidence, the “experts” operated with an unjustified certainty that their interventions were based on following “The Science™.” At every turn, when criticized or questioned, they would default back to an appeal to authority; that the consensus in the scientific community unequivocally believed that the evidence showed that lockdowns, mandates, travel restrictions, and other NPIs were based on the best available information.

After initially determining that the UK should follow Sweden’s example and incorporate a more hands-off approach that relied on protecting the elderly while allowing immunity to build up amongst the younger, healthy populations, Boris Johnson panicked, at the behest of Neil Ferguson, and terrified expert groups. Tossing out decades of planning out of fear, while claiming publicly to be following science.

Instead, a systemic, detailed review of the evidence base relied on by those same experts has now concluded that there never was any high-quality information suggesting that pandemic policies were justifiable. Only wishful thinking from an incompetent, arrogant, malicious “expert” community, and unthinking, unblinking compliance from terrified politicians using restrictions and mandates without care or concern for adverse effects.

While this new report wasn’t specifically designed to determine how effective NPIs were in reducing transmission, it’s clear and obvious conclusions give away that answer too.

If it were easy to prove that COVID policies and mandates had a positive impact on the spread of the virus, there would be dozens of high-quality studies showing a benefit. And those high-quality studies would be covered in this report, with a strong recommendation to reinstate such mandates in future pandemics.

Instead, there’s nothing.

Just exhortations to do better next time, to follow the actual high-quality evidence and not guesswork.

Based on how little accountability there’s been for the “experts” and politicians who lied about “The Science™,” there’s little doubt that when presented with the next opportunity they’ll be sure to handle it in exactly the same way.

Abandoning evidence in favor of politics.

Reprinted from the author’s Substack

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Brownstone Institute

The Cure for Vaccine Skepticism

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From the Brownstone Institute

By Martin Kulldorff Martin Kulldorff 

The only way to restore public trust in vaccination – which has taken a big hit since the lies attending the rollout of the Covid-19 vaccine – is to put a well-known vaccine skeptic in charge of the vaccine research agenda. The ideal person for this is Robert F. Kennedy, Jr., who has been nominated to lead the Department of Health and Human Services.

At the same time, we must put rigorous scientists with a proven track record of evidence-based medicine in charge of determining the type of study designs to use. Two ideal scientists for this are Dr. Jay Bhattacharya and Dr. Marty Makary, who have been nominated to lead the NIH and FDA, respectively.

Vaccines are – along with antibiotics, anesthesia, and sanitation – one of the most significant health inventions in history. First conceived in 1774 by Benjamin Jesty, a farmer in Dorsetshire, England, the smallpox vaccine alone has saved millions of lives. Operation Warp Speed, which rapidly developed the Covid vaccines, saved many older Americans. Despite this, we have seen a sharp increase in general vaccine hesitancy. Vaccine scientists and public health officials who did not conduct properly randomized trials made false claims about vaccine efficacy and safety and established vaccine mandates for people who did not need the vaccines, sowing suspicion and damaging public trust in vaccination.

What went wrong? The purpose of the Covid vaccines was to reduce mortality and hospitalization, but the randomized trials were only designed to demonstrate short-term reduction in Covid symptoms, which is not of great public health importance. Since the placebo groups were promptly vaccinated after the emergency approval, they also failed to provide reliable information about adverse reactions. Despite these flaws, it was falsely claimed that vaccine-induced immunity is superior to natural infection-acquired immunity and that the vaccines would prevent infection and transmission.

Governments and universities then mandated the vaccines for people with superior natural immunity and for young people with very low mortality risk. These mandates were not only unscientific but with a limited vaccine supply, it was unethical to vaccinate low-mortality-risk people when the vaccines were needed by older high-risk people around the world.

Since government and pharmaceutical companies lied about the Covid vaccine, are they also lying about other vaccines? Skepticism has now spread to tried-and-true vaccines that are proven to work.

And there are real, unanswered vaccine safety questions. Seminal work from Denmark has shown that vaccines can have both positive and negative non-specific effects on non-targeted diseases, and that is something that must be explored in greater depth. Vaccine Safety Datalink (VSD) scientists studying asthma and aluminum-containing vaccines concluded that while their “findings do not constitute strong evidence for questioning the safety of aluminum in vaccines…additional examination of this hypothesis appears warranted.”

While VSD and other scientists should continue to do observational studies, we should also conduct randomized placebo-controlled vaccine trials, as RFK has advocated. Since we have herd immunity for many diseases, such as measles, trials can be ethically conducted by randomizing the age of vaccination to, for example, one versus three years old, while spreading the trial over a large geographical area so that the unvaccinated are not all living close to each other.

I am confident that most vaccines will continue to be found safe and effective. While some problems may be found, that is more likely to increase rather than decrease vaccine confidence. For instance, it was found that the measles-mumps-rubella-varicella (MMRV) vaccine causes excess febrile seizures in 12- to 23-month-old children. MMRV is now only given as a second dose to older children, while the younger kids get separate MMR and varicella vaccines, resulting in fewer vaccine-induced seizures that scare parents. Although safety studies were inconclusive, it was also wise to remove mercury from vaccines. Even if we end up with fewer vaccines in the recommended vaccine schedule, that’s not necessarily a terrible thing. Scandinavia has a very healthy population with fewer vaccines in their schedules.

We won’t restore vaccine confidence by preaching to the choir. After the Covid debacle, Kennedy’s stated goal is to return to evidence-based medicine free from conflicts of interest. Letting him do that is the only way that skeptics will trust vaccines again, and those of us who trust vaccines have no reason to be afraid of that.

Attempts by the public health and pharma establishments to derail the nominations of RFK, Bhattacharya, and Makary are the surest way to further increase vaccine hesitancy in America. The choice is stark. We cannot let lopsided “pro-vaccine scientists” who clamp their hands over their ears at the mildest questions do any more harm to vaccine confidence. As a pro-vaccine scientist, and in fact, the only person ever being fired by the CDC for being too pro-vaccine, the choice is clear in my mind. To restore vaccine confidence to previous levels, we must support the nominations of Kennedy, Bhattacharya, and Makary.

Republished from RealClearPolitics

Author

Martin Kulldorff

Martin Kulldorff is an epidemiologist and biostatistician. He is Professor of Medicine at Harvard University (on leave) and a Fellow at the Academy of Science and Freedom. His research focuses on infectious disease outbreaks and the monitoring of vaccine and drug safety, for which he has developed the free SaTScan, TreeScan, and RSequential software. Co-Author of the Great Barrington Declaration.

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Brownstone Institute

Big Pharma Continues to Hide the Truth

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From the Brownstone Institute

By  Harvey Risch 

On Thursday, Joe Rogan and Marvel megastar Josh Brolin traded stories about the preponderance of Covid vaccine injuries among their friends. Brolin even described contracting “a mild case of Bell’s palsy” earlier this year, which Rogan attributed to the vaccine, noting he knew several people who suffered facial paralysis following Covid vaccination.

There is no perfect medicine. The benefits and harms of any treatment must be carefully considered in order to prescribe the safest, most effective course of action for a patient. While the FDA and CDC continue to extol the benefits of the Covid vaccines, they have ignored a growing body of evidence that these products can also be harmful. The code of medical ethics demands a transparent and balanced accounting of their impact on the American people. Only then can we set the best course for healthcare policy and future pandemics.

An honest accounting begins with clinical trials, supposedly “the most rigorous in history.” Pfizer’s own legal arguments suggest otherwise. Responding to a whistleblower lawsuit alleging major deviations from protocol, Pfizer’s lawyers noted that the company’s “Other Transactions Authority” agreement (OTA) with the Pentagon didn’t require clinical trials to comply with FDA regulations because the vaccine was a military prototype for “medical countermeasures.” This agreement allowed Pfizer to “grade its own homework,” so to speak — a point emphasized by DOJ lawyers in a separate filing in Pfizer’s support.

The FDA intended to keep Pfizer’s data hidden for 75 years, but attorney Aaron Siri’s FOIA lawsuit forced the agency to release them. Naomi Wolf’s DailyClout led 3,250 volunteer experts in analyzing more than 450,000 pages of internal Pfizer documents and uncovered massive harms ignored by the FDA, detailed in The Pfizer Papers: Pfizer’s Crimes Against Humanity.

This effort revealed 1,233 deaths in the first three months of the vaccine rollout, and a litany of injuries: “industrial-scale blood diseases: blood clots, lung clots, leg clots; thrombotic thrombocytopenia, a clotting disease of the blood vessels; vasculitis, dementias, tremors, Parkinson’s, Alzheimer’s, epilepsies.”

These harms are echoed by data from V-safe, a smartphone-based tool created by the CDC. Among 10.1 million registered V-safe users, 7.7 percent reported side effects so serious they were compelled to seek medical care, many more than once.

The main culprit is the Covid spike protein encoded in the vaccine’s mRNA technology. This protein is an antigen, or foreign immunogenic substance, located on the outer coat of the SARS-CoV-2 virus, that triggers an immune response. The mRNA in the shots instructs the body’s cells to produce identical spike proteins, inducing the immune system to create antibodies that bind to them, theoretically protecting vaccinated individuals against the virus. Unfortunately, this plan has a fatal flaw: The spike itself is toxic and potentially deadly.

Hundreds of peer-reviewed articles have demonstrated the spike’s potential for harm independent of the rest of the virus. Potential complications include myocarditis, blood clots, neurological injuries, and immune dysfunction. Pfizer’s own pre-market biodistribution studies show that vaccine components leave the injection site in the arm and penetrate every major organ system within hours, where mRNA can linger for weeks, forcing cells to churn out more and more of the toxic spike protein, which can persist for months. There is no way to predict how much spike protein the mRNA injections will produce in any individual, and there is no “off switch.”

According to CDC figures analyzed in Toxic Shot: Facing the Dangers of the COVID “Vaccines,”  from 2021-2023 the US suffered 600,000 excess deaths not associated with Covid. Furthermore, Bureau of Labor Statistics data reveal that two million Americans became newly disabled, with unusual excesses in historically low-risk groups.

These trends coincided with mass Covid vaccination, including an unaccountable 59 percent surge in deaths among Americans ages 15-44 in the third quarter of 2021 compared to 2019. Crucially Covid contributed only part of this excess mortality: in that quarter the US suffered around 201,000 excess deaths, with Covid officially accounting for 123,000, leaving 78,000 excess deaths — 39 percent of the total — still unexplained.

Similar figures from abroad underscore a tragic loss of life among healthy people at minimal serious risk from the virus.

It could get worse. No carcinogenicity studies were performed on the injections prior to their launch, thus long-term cancer risks are essentially unknown. The spike protein also appears prone to prion-like misfolding, raising the specter of potential neurodegenerative disorders.

Medical ethics demand a balanced approach to every intervention, weighing potential benefits against potential harms. However, in the case of the Covid vaccines, federal agencies have chosen only to proclaim benefits. By surfacing data that bear upon both the positive and negative impacts of the Covid vaccines, and evaluating the pandemic performance of CDC, FDA, and other health agencies, the new administration can restore confidence and integrity in medicine and public health.

Republished from The Federalist

Author

Harvey Risch, Senior Scholar at Brownstone Institute, is a physician and a Professor Emeritus of Epidemiology at Yale School of Public Health and Yale School of Medicine. His main research interests are in cancer etiology, prevention and early diagnosis, and in epidemiologic methods.

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