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Theoretical Vaccine Effectiveness for Novavax Unacceptably Low

Real World Study Disappointing for Non-Genetic Vaccine

By Peter A. McCullough, MD, MPH | Courageous Discourse | October 11, 2023

If it came to forced COVID-19 vaccination against human will, I have said Novavax would be the choice since it gives a limited 5 mcg dose of the potentially lethal Spike protein and has no genetic material. The growing number of fatal side effects with mRNA vaccines and recent news of contamination with SV-40 cDNA has resulted in record low rates of booster uptake, currently at 1.3% of unwary Americans.

Mateo-Urdiales reported on 20,903 individuals who took the two shot primary series of Novavax. Theoretical vaccine effectiveness was shockingly low:

“Adjusted estimated vaccine effectiveness against notified SARS-CoV infections in those with partial vaccination (15 days after the first dose to 14 days after the second dose) was 23%(95%CI, 13%-33%), increasing after full vaccination to 31% (95%CI, 22%-39%). Estimated vaccine effectiveness was higher against symptomatic COVID-19, with an estimate of 31% (95%CI, 16%-44%) in those partially vaccinated and of 50% (95%CI, 40%-58%) in those fully vaccinated.”

Mateo-Urdiales A, Sacco C, Petrone D, et al. Estimated Effectiveness of a Primary Cycle of Protein Recombinant Vaccine NVX-CoV2373 Against COVID-19. JAMA Netw Open. 2023;6(10):e2336854. doi:10.1001/jamanetworkopen.2023.36854

If a vaccine cannot safely provide at least 50% protection for a year, it is not viable in my clinical practice. Sadly Novavax failed at both of these outcomes. With low-risk Omicron, and likely substantial natural immunity by Fall of 2022, only 26 infections led to hospitalization during the study period; 1 occurred during the reference period, 7 during partial vaccination, and 18 after full vaccination. No deaths were reported.

In summary, Novavax is probably the safest of all the COVID-19 vaccines because it does not use genetic technology. Sadly, it is useless against Omicron and cannot be recommended for any health benefit.

 

October 13, 2023 Posted by | Science and Pseudo-Science | | Leave a comment

Lawsuit Pushes Back Against California Medical Board’s “Misinformation” Censorship Power

By Didi Rankovic | Reclaim The Net | October 12, 2023

A lawsuit has been amended in California against this US state’s medical boards’ “misinformation powers” – based on a law that is soon to be repealed, and which critics – some of them legal plaintiffs – say allowed the government to prevent them from practicing medicine, the way they were trained to do.

It was one of the rules, called Assembly Bill 2098 (AB 2098), introduced to keep medical professionals in check, in case they felt like speaking their minds freely as insights into Covid were developing.

And since the world has now moved on to other crises, the “forgotten pandemic” censorship laws are getting “quietly” repealed.

But not really, the plaintiffs in this case claim – because of the nature of the repeal of the short-lived AB 2098, made null-and-void on September 14 via Senate Bill 815 (SB 815). California Senator Newsom got to sign all three documents.

However, the repeal – which will not be in effect before the start of 2024 – at the same time incorporates Democrat member of California Assembly Evan Low’s provision that doctors who get accused of “misinformation” can still be punished – “held accountable” – regardless of whether the controversial law was actually applicable.

“The Medical Board of California will continue to maintain the authority to hold medical licensees accountable for deviating from the standard of care and misinforming their patients about COVID-19 treatments,” Low said.

How in the world is this political, ideological, pre-election, and legal gymnastics even supposed to work?

The lawsuit against the bill, Hoang et al. v. Bonta et al., has the plaintiffs represented by California attorney Richard Jaffe.

He had this to say: “Because of the repeal of AB 2098, and the board’s position that it can still sanction the speech targeted by the soon-to-be-repealed law, we are pivoting in our lawsuit and arguing to the judge that they can’t do it under their general statute either because the speech does not change just because the legal theory/statute changes.”

The world clearly has moved to other crises – but it seems, not the California Democrats. And so the plaintiffs in the lawsuit’s amended format are also asking to add more to their ranks. One of the original ones is Children’s Health Defense (CHD).

However absurd the “standard of care” argument that supersedes a law may seem to a layperson, Jaffe is obviously taking it seriously.

The court will hear the arguments related to this new development on November 13.

October 12, 2023 Posted by | Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science | , , , , | Leave a comment

Yes, Treating COVID Patients With Hydroxychloroquine Can Save Lives

By Angelo DePalma, Ph.D. | The Defender | October 11, 2023

Hospitalized COVID-19 patients treated with hydroxychloroquine (HCQ) alone, or HCQ plus the antibiotic azithromycin, had significantly lower mortality than those not receiving the drugs, according to a study released this month in New Microbes and New Infections.

Researchers in Belgium report that just 16.7% of COVID-19 patients given HCQ, with or without azithromycin, died within 28 days compared to 25.9% among those not taking HCQ — a 35% lower mortality.

After adjusting for age differences, the risk of death was still 24% lower for HCQ-treated hospitalized patients.

The survival benefit was seen across all ages and was statistically significant.

The results support the efficacy of HCQ and azithromycin in improving outcomes for hospitalized COVID-19 patients. This contrasts with earlier studies using dangerously high HCQ doses that found no benefits.

Who participated in the study?

Led by Dr. Gert Meeus, a nephrologist at AZ Groeninge Hospital, Kortrijk, Belgium, researchers collected data from March 16 to May 20, 2020 — the first few months of the pandemic.

They compared outcomes for 352 COVID-19-positive, HCQ-treated adults hospitalized at AZ Groeninge Hospital with those of 3,533 patients across Belgium who did not receive the drug.

Treated patients averaged 69.7 years versus 73.1 years for the control group. While this age difference favors the younger subjects who face less risk from the virus, this factor was more than offset by the treatment group’s higher incidence of high blood pressure, diabetes, liver and lung diseases, and weakened immunity.

Treated subjects were also more obese — a COVID-19 risk factor — with lower blood oxygen (suggesting severe illness) and higher C-reactive protein levels. C-reactive protein is a blood marker for inflammation and poor COVID-19 outcomes.

During the 28 days following initial treatment, 16.7% of patients who received HCQ, either alone or with azithromycin, died compared with 25.9% in the control group.

How was HCQ administered?

For the study, 299 patients (85%) received HCQ plus azithromycin versus 53 who took HCQ alone. Researchers only prescribed the antibiotic when they suspected bacterial pneumonia. Data for HCQ alone and HCQ plus azithromycin were combined.

Subjects received HCQ as two 400-milligram doses on day one and two 200-milligram doses on days two through five.

Patients younger than 75 years received 500 milligrams of azithromycin for five days. Older patients took 500 milligrams on day 1 and 250 milligrams per day for four days.

88% of patients received the full treatment course but 12% took the drugs for less time, at the caregiver’s discretion, due to side effects or reaching a terminal condition.

Otherwise, side effects observed in 197 patients were mild and mostly stomach issues. One patient had hallucinations and two developed a skin rash.

Thirteen patients dropped out of the study due to side effects, including 4 of 15 who developed heart muscle abnormalities — despite an earlier study reporting an association between HCQ and lower cardiovascular risk.

Nine patients dropped out because of digestive upset. One patient developed an abnormal but nonfatal post-study heart rhythm, but no treated patients experienced sudden death or irregular heartbeat during the study.

How the drugs work

HCQ and azithromycin work together to eliminate the COVID-19 virus, but the drugs may benefit patients in other ways.

Both drugs act on the immune system in ways that may suppress the COVID-19 cytokine storm responsible for much of COVID-19-related illness and death.

HCQ may also prevent blood clots in COVID-19 patients, while azithromycin may prevent additional, non-lung bacterial infections.

HCQ was approved in the U.S. in 1955 to treat malaria, but because of its anti-inflammatory effects it is also prescribed to adults to treat autoimmune diseases like lupus and rheumatoid arthritis.

Most serious side effects — including retinopathy, which causes blindness — occur after years of use, while COVID-19 treatments generally last for less than one week.

The World Health Organization lists HCQ as an “essential medicine” based on its “safety, efficacy and public health relevance.”

Study strengths and weaknesses

Meeus designed his study and interpreted his findings to include results that may not have supported the “safety and efficacy” of HCQ.

For example, all patients receiving at least one dose of HCQ were included in the treatment group regardless of whether they completed the study. One dose of HCQ was unlikely to affect their survival, but including such patients would have increased mortality numbers in the treatment group, thereby underestimating HCQ survival benefits.

Excluding very sick patients in a survival study tends to make data appear stronger because fewer deaths invariably occur among healthier subjects. Meeus and coworkers did not do this.

Meeus’ results also likely underestimated the benefits of HCQ treatment by reviewing patients only after hospitalization, when they were already quite sick. COVID-19 treatment experts stress the importance of treatment before patients reach this stage.

This retrospective study associated a current outcome (death) with an earlier effect (receiving HCQ). Retrospective studies are less capable of establishing causation than prospective studies that first look at the intervention or cause and only later for effects.

Another potential study shortcoming involves the statistics investigators chose to report HCQ’s benefits. A reduction in deaths from 25.9% to 16.7% is a 36.5% decrease, but the effect is smaller when survival, not death, is the outcome measured.

Death rates of 25.9% and 16.7% mean that 83.3% of treated and 74.1% of untreated patients survived, for an overall survival benefit under 10%.

Reporting relatively large differences between two small numbers is a common strategy for amplifying modest clinical benefits.

Meeus did not account for the many observational studies carried out by such doctors as Didier RaoultVladimir ZelenkoPierre KoryPeter McCullough and others using HCQ with azithromycin and/or zinc to treat COVID-19 beginning in 2020 — some with very large practices — all demonstrating significant benefits with early treatment.

He also did not review early treatment randomized control trials or the many other studies showing clear benefits of HCQ treatment.

Conclusion: ‘remarkable’ results

The authors described their results as “remarkable” since large HCQ studies during the first pandemic year showed no benefit.

However, where Meeus and co-workers used HCQ at standard doses, the earlier trials used a fourfold higher total dose, including an initial dose seven times higher than the maximum approved dosage.

For example the WHO “Solidarity” and U.K. “Recovery” clinical trials used HCQ dosages that were considered fatal.

According to Meeus, other studies (see herehere, and here) using more reasonable HCQ dosing failed because they did not recruit enough subjects to show a statistically significant effect.

One of these studies found a 44% reduction in death at 28 days but included too few patients to be able to claim an HCQ benefit.

Percentage of patients who died in the HCQ group (white bars) vs. the no-HCQ group (black bars) by age group. A survival benefit was seen in all age groups. While about 2.5% of untreated 31- to 44-year-olds died during the study, no treated patients in this age group died. Credit: Gert Meeus et al.

Meeus concluded:

“Our study suggests that, despite the controversy surrounding its use, treatment with hydroxychloroquine and azithromycin remains a viable option. The favorable results and reassuring safety data support the need for adequately powered confirmatory randomized controlled trials using low dose hydroxychloroquine plus azithromycin.

“Given the pandemic emergency it is reasonable to give this treatment the benefit of the doubt pending the results of these trials or the advent of better treatment options.”


Angelo DePalma, Ph.D., is a science reporter/editor for The Defender.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

October 12, 2023 Posted by | Science and Pseudo-Science, Timeless or most popular, War Crimes | , | Leave a comment

Nothing To Sea Here Folks

Climate Discussion Nexus | October 2, 2023

In this “Fact Check” video from the Climate Discussion Nexus, Dr. John Robson expands on our Sea Level Check series to rebut claims of dangerous, accelerating, man-made sea level rise by examining the actual history and current state of melting land ice, changes in the land and other complex factors that contribute to this non-crisis.

To support the Climate Discussion Nexus, subscribe to our YouTube channel (http://www.youtube.com/channel/UC_egd…, our Rumble channel (https://rumble.com/user/ClimateDN), our newsletter (at http://www.climatediscussionnexus.com/) and our podcast on Spotify (https://open.spotify.com/show/6IX3QVN…) and Google (https://podcasts.google.com/feed/aHR0…, like us on Facebook (http://www.facebook.com/ClimateDN/), follow us on Twitter (http://www.twitter.com/ClimateDN) and Gettr (https://www.gettr.com/user/climatedn).

October 12, 2023 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | Leave a comment

FDA HEAD GOES ANTI-VAX

The Highwire with Del Bigtree | October 5, 2023

Once labeled a dangerous ‘anti-vax’ technique, head of the FDA’s Center for Biologics Evaluation and Research, Dr. Peter Marks is now stating he would space out vaccines to avoid mounting adverse reactions.

October 11, 2023 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | Leave a comment

BANNED: Book by Dr. Peter McCullough & John Leake

BY JOHN LEAKE | COURAGEOUS DISCOURSE | OCTOBER 9, 2023

I would like to open this column by stating that I have long had a great relationship with Amazon, which has sold far more of my books than have ever been sold in bookstores. I have also been extremely grateful to Amazon’s Kindle Direct Publishing program for empowering me to publish whatever nonfiction books I please, quickly and efficiently, while retaining the rights and earning the best royalty in the business.

In May 2022, Dr. McCullough and I published our book, The Courage to Face COVID-19: Preventing Hospitalization and Death While Battling the Bio-Pharmaceutical Complex, directly on Amazon. Quickly the book became a hit and within a year it had earned over 1000 5-Star Reviews. For almost 3 weeks in July 2022 it was a top 100 seller.

In the autumn of last year, Tony Lyons, President and Publisher of SKYHORSE in New York, graciously offered to bring out a special, handsome hardcover edition with a preface by U.S. presidential candidate, Robert F. Kennedy, Jr., who warmly endorsed our work.

A bit of Covid fatigue this year caused sales to decline, but in September the book got a second wind as more and more Americans seem to be recognize that Dr. McCullough has been right all along.

To my gratitude and delight, Amazon actually supported the effort by running a deep discount promotion while still paying the same royalty to us—an act of generosity to authors that is unheard of in traditional publishing.

And then, on September 29, seemingly out of nowhere, Amazon Account Review sent me the following notice:

We have temporarily suspended your KDP account because we found offensive content that violates our Content Guidelines in the title(s) listed below:
ASIN: B09ZLVWMD9 –
Title: THE COURAGE TO FACE COVID-19: Preventing Hospitalization and Death While Battling the Bio-Pharmaceutical Complex – Author: John Leake

Upon receiving this message, I humbly beseeched Account Review to restore my account and to let me know what “offensive content” was found in our book. Amazon restored my account and published my latest book—a conventional work of true crime—but refused to reinstate The Courage to Face COVID-19. Yesterday my third appeal was turned down without answering my query about what in our book is offensive.

My question seemed especially pertinent, given that Account Review provided me with a link to its Content Guidelines, which include a section on Offensive Content.

Offensive content

We don’t sell certain content including content that we determine is hate speech, promotes the abuse or sexual exploitation of children, contains pornography, glorifies rape or pedophilia, advocates terrorism, or other material we deem inappropriate or offensive.

Obviously, nothing in our book even remotely touches on any of these subjects. Upon reading this description, it occurred to me that it was a perfection description of 120 Days of Sodom, by the Marquis de Sade, which contains hundreds of pages that glorify the abuse and sexual exploitation of children, violent pornography, and glorifications of rape and pedophilia. I did a quick search for the title, and voila, there it is, for sale on Amazon in three formats.

None of my polite entreaties to Content Review was answered with an explanation of what, in our book, is offensive or in violation of any other published guideline. This strengthened my suspicion that the decision was the result of a sudden imposition of power for which the Content Review staff was not prepared.

Even more stunning than banning my softcover edition was Amazon’s decision to ban Tony Lyons’s SKYHORSE hardcover edition from the site without even sending the publisher notice. He learned of his edition’s demise from me.

This is a developing story about arbitrary censorship and book banning. Generally speaking, Amazon has a robust history of resisting pressure to ban books. Even during the COVID Pandemic, Amazon bucked the censorship regime that was established at Facebook, YouTube, and Twitter.

I believe it is no exaggeration to state that Amazon’s decision to ban our work of medical and historical scholarship, carefully vetted by Dr. Peter McCullough—who has published over 600 peer-reviewed papers in top academic medical journals—is the most egregious act of arbitrary censorship in the history of American publishing.

Many works of literature have been banned from public school systems and libraries and censured by religious organizations. However, I cannot find a single example of a banned nonfiction book that contains zero sex, zero violence, zero expletives, zero harshly expressed opinions, and zero assertions that aren’t grounded on rock solid scholarship.

Indeed, the book is a strictly factual narrative based on hundreds of published sources ranging from academic papers to standard works of medical history to documents published by U.S. federal agencies. The longest chapter in the book recounts Dr. McCullough’s U.S. Senate testimony on November 19, 2020.

This is a developing story about a gross infringement of the freedom of speech that is enshrined in the First Amendment of the U.S Constitution. Coincidentally, tomorrow (October 10) I have been invited to address the Republican Women of Greater North Texas about the critical importance of maintaining free speech for the maintenance our Constitutional Republic. I can now speak from very personal experience.

I would like to conclude by stating that I believe this decision is almost certainly the result of outside pressure being brought to bear on Amazon—the sort of outside pressure from the U.S. Executive Branch that was revealed in discovery in Missouri v. Biden.

As Jacob Siegel recently remarked in a brilliant piece in Tablet magazine titled “A Guide to Understanding the Hoax of the Century:”

At companies like Facebook, Twitter, Google, and Amazon, the upper management levels had always included veterans of the national security establishment. But with the new alliance between U.S. national security and social media, the former spooks and intelligence agency officials grew into a dominant bloc inside those companies; what had been a career ladder by which people stepped up from their government experience to reach private tech-sector jobs turned into an ouroboros that molded the two together.

I strongly suspect that the banning of our book from Amazon has the fingerprints of Biden administration or intelligence agency goons all over it.

For those who would still like to purchase our book, please visit our website by clicking on the image below.

October 10, 2023 Posted by | Book Review, Full Spectrum Dominance, Progressive Hypocrite, Science and Pseudo-Science | , | Leave a comment

Another Tacit Admission That COVID Mandates Were a Disastrous Mistake

By Ian Miller | Brownstone Institute | October 9, 2023

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.

Ian Miller is the author of “Unmasked: The Global Failure of COVID Mask Mandates.” 

October 10, 2023 Posted by | Civil Liberties, Science and Pseudo-Science | , , , | Leave a comment

Doctor Persecuted For “Misinformation” Wins Appeal

By Cindy Harper | Reclaim The Net | October 8, 2023

Subverting the tightening noose of censorship, the judicial system has risen, this time at least, as a defender of free expression and professional discourse in Washington State. The Court of Appeals has recently extended a lifeline to Dr. Richard Eggleston, a retired ophthalmologist, in his battle against the Washington Medical Commission’s (WMC) accusations of spreading “misinformation” about COVID-19. This pivotal ruling not only resonates as a triumph for Dr. Eggleston but also echoes across the medical community, bolstering the principle that the crucible of critical discourse should not be chilled by punitive actions.

We obtained a copy of the ruling for you here.

Dr. Eggleston, from Clarkston, Washington, had penned a sequence of critiques last year in the Lewiston Morning Tribune, challenging the prevailing narratives around COVID-19, specifically deliberating on the safety and veracity of the vaccines. His audacity led to an avalanche of disciplinary actions spearheaded by the WMC in August 2022. Accused of unprofessional conduct and “willful misrepresentation of facts,” the retired eye doctor found himself thrust into the cauldron of a legal and professional maelstrom.

As the waves of allegations crashed down, Eggleston invoked his First Amendment right to free speech, refuting the charges with a motion to dismiss. The WMC’s refusal to honor his motion nudged him to escalate the matter to the courts. His quest for justice first encountered a roadblock when the Washington State Superior Court denied his appeal for an injunction. Undeterred, Eggleston propelled his case to the Court of Appeals, which in a moment of judicial prudence, awarded him an emergency injunction in May, halting the impending court proceedings.

The saga witnessed a fresh chapter last week when Court of Appeals Commissioner Hailey L. Landrus sanctioned Eggleston’s motion for a discretionary review of the previous court’s verdict. Attorney Richard Jaffe, representing Eggleston, lauded the decision as “very good news for all who believe that doctors should be able to publicly criticize” what he termed as COVID-19 “propaganda.” This sentiment was echoed by another counsel for Eggleston, Todd Richardson, who expressed both gratitude and relief at the verdict.

October 10, 2023 Posted by | Full Spectrum Dominance, Science and Pseudo-Science | , , | Leave a comment

Fluoride Lawsuit Captures Shocking Admissions On The Record

The Highwire with Del Bigtree | October 5, 2023

The Fluoride Lawsuit has produced video admissions that may have exposed the nearly 80 year practice of adding the toxin to our nation’s water supply as one of the biggest public health scandals in American history. Attorney Michael Connett, Esq., explains how adding fluoride to drinking water became standard practice in the US and shares the studies that link it with severe disease. Then, he shares exclusive video of court depositions of experts you have to see to believe.

October 9, 2023 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | Leave a comment

The Nutritional ‘Dark Matter’ in Your Food — And Why Synthetic Food Is So Dangerous

By Dr. Joseph Mercola | October 4, 2023

Do you know what’s in the food you eat? Remarkable as it may seem, 99% of the components making up whole food are a complete mystery.

As reported by New Scientist in July 2020:

“We know next to nothing about the vast majority of compounds in our diet … ‘Our understanding of how diet affects health is limited to 150 key nutritional components,’ says Albert-László Barabási at Harvard Medical School, who coined the term nutritional dark matter.

“‘But these represent only a small fraction of the biochemicals present in our food’ … The idea that food is a rich and complex mix of biochemicals is hardly news.

“Even the well-known macronutrients — proteins, carbohydrates and fats — are hugely diverse. There’s also a vast supporting cast of micronutrients: minerals, vitamins and other biochemicals, many of which are only present in minuscule quantities, but which can still have profound health effects.”

The official source of nutritional information is the USDA’s National Nutrient Database for Standard Reference.

It lists the composition of hundreds of thousands of foods, but it’s not as detailed as you might imagine.

In all, it details only 188 nutritional components, including 38 flavonoids, yet scientists estimate there are more than 26,000 different biochemicals in our food.

As noted by New Scientist : “With the USDA as your guide, 99.5% of the components in food are a mystery,” and as noted by Barabási, “It would be foolish to dismiss 99.5% of the compounds we eat as unimportant … We will not really understand how we get sick if we don’t solve this puzzle.”

Searching for nutritional ‘dark matter’

Disturbed by the information gap, an international team of researchers started working on a more comprehensive database a decade ago called FooDB, which as of 2020 contained information on some 70,000 nutritional compounds.

Yet even this database still has a long way to go. An estimated 85% of the nutritional components listed remain unquantified, meaning they know a food contains a particular component, but they don’t know how much.

The health implications of most compounds also remain largely unknown.

New Scientist notes:

“This is also true of individual micronutrients. ‘Consider beta-carotene,’ says Barabási. ‘It tends to be positively associated with heart disease, according to epidemiological studies, but studies adding beta-carotene to the diet do not show health benefits. One potential reason is that beta-carotene never comes alone in plants; about 400 molecules are always present with it. So epidemiology may be detecting the health implications of some other molecule.’

“Another probable cause is the effect of the microbiome on dark nutrients, says [FooDB founder David] Wishart. ‘Most dark nutrients are chemically transformed by your gut bacteria.’

“That’s probably why studies on the benefits of different foods give relatively ambiguous results. We don’t properly control for the variation in gut microflora, or our innate metabolism, which means different people get different doses of metabolites from their food.”

Processed foods are an even greater mystery

The reason I started with that background is because we know even less about the constituents of processed foods and synthetic foods that ignorantly claim to be “equivalents” to whole foods, such as “animal-free meats” or “animal-free milk.”

Food processing alone will often alter the composition of bioactive molecules in a food and hence the food’s impact on health, but today, processed foods also contain a wide array of synthetic chemicals that, prior to the modern era, were never part of the human diet.

As such, they pose incredible risks to long-term health and well-being. Processed foods may also have intergenerational effects.

In recent years, the idea that we can simply replace whole foods with synthetic, genetically modified or lab-grown alternatives that are wholly equivalent to the original food has taken root. In reality, that’s simply impossible.

How can scientists create equivalence when they don’t even know what 85% or more of the whole food they’re trying to replicate consists of?

Common sense will tell you they can’t. It might look, smell and even taste similar, but the micronutrient composition will be entirely different, and as a result, the health effects will be incomparable as well.

Animal-free equivalence is a PR fraud

Take cultured meat, for example. It’s said to be equivalent to real animal meat because it’s grown from animal cells. The cells are then grown in a nutrient solution inside a bioreactor until they become a meat-like slab.

Similarly, Bored Cow animal-free milk is a dairy alternative made with whey protein obtained through a fermentation process, plant-based fats (in lieu of milk fats), citrus fiber (for creaminess) and added vitamins and minerals.

Defenders of cultured meat insist that this product is not “fake meat” but “actual meat,” the only difference is that no animal had to be slaughtered to create it.

Cultured meat and other synthetic foods are also said to be more environmentally friendly. But nothing could be further from the truth.

Their impact is far more akin to that of the pharmaceutical industry than the food industry.

According to a recent “cradle-to-gate life cycle” analysis, the lab-grown meat industry produces anywhere from four to 25 times more CO2 than traditional animal husbandry.

Based on this assessment, each kilo of cultured meat produces anywhere from 542 pounds (246 kilos) to 3,325 pounds (1,508 kg) of carbon dioxide emissions, four to 25 times greater than that of conventional beef.

And this information is only provided to refute those who believe the global warming fallacy.

As noted by the authors, investors have poured billions of dollars into the animal cell-based meat sector based on the theory that cultured meat is more environmentally friendly than beef.

However, according to these researchers, that hype is based on flawed analyses of carbon emissions.

Cultured meat is also the epitome of ultra-processed food and therefore likely to cause health problems like those caused by other ultra-processed foods, such as obesitycardiovascular diseases, Type-2 diabetes, metabolic syndrome, irritable bowel syndrome, cancermental health problems and increased all-cause mortality.

A paper published in the April issue of Animal Frontiers also warned that there are several implications of cell-based meat that need to be considered but aren’t, including the fact that cultured products are not nutritionally equivalent to the meats they’re intended to replace.

The claim that no animals are killed in the process is also false. At present, most cultured or cell-based meats are created by growing animal cells in a solution of fetal bovine serum, which is made from the blood of unborn calves.

In short, pregnant cows are slaughtered to drain the unborn fetus of its blood.

Is it safe to eat tumors?

There are also many unanswered questions surrounding safety. For example, to get the cell cultures to grow, some companies are using immortalized cells, which technically speaking are precancerous and/or fully cancerous.

(Other companies use embryonic stem cells or cells from living animals.)

The reason for using immortalized cells is that normally behaving cells cannot divide forever. Most cells will only multiply a few dozen times before they become senescent (old) and die.

This won’t work when your intention is to grow thousands of pounds of tissue from a small number of cells, hence they use immortalized cells that have no off switch for their replication and can divide indefinitely.

Meat substitutes cultured in this way could therefore be thought of as tumors, seeing how the flesh is entirely made up of precancerous or cancerous cells. Is it safe to eat tumors? We don’t know.

Massachusetts Institute of Technology biologist Robert Weinberg, Ph.D., has proposed that humans can’t get cancer from these cells because they’re not human cells and therefore cannot replicate inside your body.

However, there’s no long-term research to back this theory.

Dietary headaches to come

It’s also important to realize that the nutritional composition and safety of synthetic foods will vary depending on the brand.

When you’re dealing with beef, for example, the meat from one cow will be relatively identical to that of any other cow (one major exception being the way they’re raised and fed).

One wild-caught salmon is comparable to any other wild-caught salmon and each russet potato is more or less identical to every other russet potato.

However since each synthetic food brand uses proprietary ingredients and processes, no two will have identical composition or safety, so even if one is eventually proven safe and nutritious, those results cannot be applied to any other brand.

This variance has the potential to create major problems in the future when all sorts of foods have been replaced with synthetic non-equivalents.

How do you determine which cultured beef, chicken or salmon brand might be best for you? How will you devise a sensible diet plan when every food comes in myriad variations of varying composition and safety?

Synthetic foods pose unique food-safety hazards

Many synthetic food proponents claim lab-created food will bypass a host of food-safety problems, but the converse is far more likely to be true.

Sure, beef, for example, can be contaminated during processing, packaging, transport or storage, or during the cooking process.

But in cultured meat, every ingredient and processing step brings with it the potential of contamination and any of the hundreds of ingredients could have toxic effects, alone or in synergy.

Indeed, an in-depth analysis of the available evidence by the Food and Agriculture Organization of the United Nations and a World Health Organization expert panel, published in May, concluded there are at least 53 potential health hazards associated with lab-grown meat.

Among them are the possibility of contamination with heavy metals, microplastics, nanoplastics and chemicals, allergenic additives, toxic components, antibiotics and prions.

What’s more, some of the ingredients that go into synthetic biology like cultured meat are regulated as “non-detectable manufacturing aids,” and you won’t even know what they are. Israeli startup Profuse Technology, for example, has developed a growth media supplement that massively encourages protein growth.

As reported by Food Navigator Europe in an article titled, “Cultivated Meat ‘Breakthrough’: Media Supplement Achieves Full Muscle Maturation on Scaffold Within 48 Hours,” the supplement reduces the time to grow filets and steaks by 80% and augments the protein in the final product by a factor of five.

An unsustainable model

The cultured meat process also produces toxic biowaste — a problem that doesn’t exist in conventional agriculture and food processing. In the video above, Alan Lewis, vice president of government affairs for Natural Grocers, reviews what goes into the making of synthetic biology.

The starting ingredients are typically cheap sugars and fats derived from genetically engineered corn and soy, grown in environmentally destructive monocultures with loads of herbicides, pesticides and synthetic fertilizers.

As a result, they’re loaded with chemical residues. Hundreds of other ingredients may then be added to the ferment to produce the desired end product, such as a certain protein, color, flavor or scent.

The most often used microorganism in the fermentation process is E. coli which has been gene-edited to produce the desired compound through its digestive process.

The microorganism must also be antibiotic-resistant since it needs to survive the antibiotics used to kill off other undesirable organisms in the vat.

As a result, antibiotic-resistant organisms also become integrated into the final product, and the types of foodborne illness that might be caused by gene-edited antibiotic-resistant E. coli and its metabolites are anyone’s guess.

In addition to the desired target metabolite, these gene-edited organisms may also spit out non-target metabolites with unknown environmental consequences and health effects. But that’s not all. Once the target organisms are extracted, what’s left over is hazardous biowaste.

While traditional fermentation processes, such as the making of beer, produce waste products that are edible by animals, compostable and pose no biohazard, the biowaste from these synthetic biology ferments must first be deactivated and then must be securely disposed of. It cannot go into a landfill.

Protect your health by avoiding ‘frankenfoods’

Making food that requires genetically modified organisms inputs and produces more CO2 than conventional farming and hazardous biowaste to boot is hardly a sustainable model.

But then again, synthetic biology and processed foods are not being pushed out of true concern for sustainability.

If that was the goal, everyone would be looking at regenerative agriculture where every part of the system supports and sustains other parts, thereby eliminating the need for chemical inputs, radically reducing water needs while optimizing yields.

No, synthetic biology is pursued because it is a formidable control mechanism. Those who own all the synthetic food production will control the world in a very literal sense. To learn more about this plot for control, see “The Fake ‘Food as Medicine’ Agenda.”

In short, the globalists already own and control most of the carbohydrates grown in the world today. By replacing real animal foods with patented lab-made protein alternatives, they’ll have unprecedented power to control the world’s population.

It’ll also grant them greater control over people’s health. It’s already known that the consumption of ultra-processed food contributes to disease, and the benefactor of ill health is Big Pharma.

The processed food industry has spent many decades driving chronic illness that is then treated with drugs rather than a better diet. Synthetic foods will likely be an even bigger driver or chronic ill health and early death.

The fact is, fake meat and dairy cannot replace the complex mix of nutrients found in grass-fed beef and dairy, and it’s likely that consuming ultra-processed meat and milk alternatives may lead to many of the same health issues that are caused by a processed food diet.

So, if you want to really protect your health and the environment, skip pseudo foods that require patents and stick to those found in nature instead.

October 7, 2023 Posted by | Environmentalism, Progressive Hypocrite, Science and Pseudo-Science, Timeless or most popular | Leave a comment

Christian Drosten: “I’ve Had Three Doses of the Vaccine and Been Infected Twice”

BY ROBERT KOGON | THE DAILY SCEPTIC | OCTOBER 7, 2023

Does anyone still remember the days when COVID-19 vaccines were reputed to do what other vaccines do – namely, prevent people from getting infected – and hence we were all taught to speak of exceptional ‘breakthrough infections’ when the unexpected, nonetheless, came to pass?

Well, Germany’s ‘state virologist’ Christian Drosten apparently does not remember them either. Drosten is a member of the German Government’s ‘Corona Expert Council’ and is treated as the absolute authority in Germany for all things COVID-19-related. He also, purely coincidentally, developed the notoriously hyper-sensitive COVID-19 PCR testing protocol, which would go a long way to create the COVID-19 pandemic based on the innumerable ‘asymptomatic cases’ it would go on to detect.

Drosten has given a new interview to the German weekly paper Die Zeit on the solemn occasion of the awarding of this year’s Nobel Prize in Medicine to Drew Weissman and Katalin Kariko, two scientists who contributed to developing the mRNA technology underlying the most widely-used COVID-19 vaccines in the West. Drosten praises the decision to award the prize to the mRNA pioneers – “the technology has proven its significance thanks to the authorisation for COVID-19” – and goes on to note that “I’ve had three doses of the vaccine and been infected twice”.

Three doses and he still got infected twice? Well, why does he agree with the Nobel Committee awarding the prize to Weissman and Kariko then?

Drosten’s remark is apparently supposed to help explain why he will not be getting the new ‘variant-adapted’ COVID-19 jab this autumn or donning a facemask when out and about: since, namely, he already has adequate immunity to fend off the virus – not, it seems, thanks to his previous vaccine doses but due to having caught the bug despite them!

Further on in the interview, Drosten makes this assumption explicit. Thus, asked whether the public has to be concerned about new, more highly transmissible Covid variants, Drosten replies:

Two years ago, higher transmissibility due to new mutations always also meant that more people got seriously ill. Simply because immunity against serious outcomes was not yet complete. By now, the overwhelming majority have built up immune defences by way of infections which are directed against the whole virus, not only against the spike protein from the vaccine. Infections were required for this.

So, Drosten now speaks (and it is not the first time) as if the idea all along was for people to get the vaccine and the virus. He adds, however, that vaccination was still worthwhile, since, he claims, it reduced the severity of the illness when people got infected. Mind you, he has just said that “complete immunity” even against severe disease is only achieved via infection.

The somewhat bewildering position adopted by Drosten is, by the way and not surprisingly – he is not referred to as Germany’s ‘state virologist’ for nothing – also the official German Government position. The official recommendation of the Standing Committee on Vaccination (STIKO) of the German public health authority is that everyone over 18 years of age should have acquired a “basic immunity” by way of at least three “antigen contacts”, either in the form of vaccine doses or infections. The STIKO, however, insists that at least two of these “contacts” should have taken place by way of vaccination, thus suggesting that vaccine-induced immunity is somehow superior to natural immunity, whereas Drosten’s remarks clearly suggest the contrary.

In its latest recommendation on the new ‘variant-adapted’ jab, moreover, the STIKO notes that “the majority of the population has already been vaccinated multiple times and has acquired good basic immunity thanks to having had SARS-CoV-2 infections in addition”. This is why, incidentally, the STIKO only recommends the adapted jab for persons over 60 and members of other ostensibly high-risk groups, but not for anyone else. But the tenor is exactly the same as in Drosten’s remarks, as if getting vaccinated and then getting sick had been the plan all along.

Well, for Drosten’s and the STIKO’s benefit, the below comes directly from the European Medicines Agency summary document on what is by far the most-widely used COVID-19 vaccine in the EU: BioNTech’s mRNA-based ‘Comirnaty’.

Comirnaty was authorised to prevent COVID-19, not to prevent severe outcomes. If it does not prevent COVID-19, it failed.

Robert Kogon is the pen name of a widely-published journalist covering European affairs. Subscribe to his Substack and follow him on X.

October 7, 2023 Posted by | Deception, Science and Pseudo-Science | , | Leave a comment

Primodos: another example of MHRA’s failure to “put patients first”

UK took 20 years to withdraw drug after harms were first made known

Health Advisory & Recovery Team | October 4, 2023

Most people are aware of Thalidomide, many are aware of Valproate, but there are several other drugs that have caused birth defects in children that are less well known including Debendox, Carbimazole and Primodos.

Primodos families achieved a main house parliamentary debate on 7th September led by Yasmin Qureshi. Whilst the House was not well attended, every single MP in the Chamber was on the side of the families and little effort was made to defend Government and regulator action.

Yasmin Quereshi explained:

“Children were born with serious deformities due to the hormone pregnancy test drug Primodos, which was taken by expectant mothers between 1953 and 1975”

“The UK regulator first received a warning about the drug in 1958. A definitive study was published in 1967, which linked birth defects to the synthetic hormones in Primodos. Baroness Cumberlege concluded that Primodos should have been removed from the market in 1967. The UK regulator failed in its duty of care to women: Primodos was eventually withdrawn in 1978, 20 years after the first warning.”

Finland, Sweden, Holland and Norway banned the use of hormone pregnancy tests at least 7 years earlier by 1971. MPs passionately recounted many stories of harm caused to their constituents, including Allan Dorans who explained the impact on Nan’s daughter Michelle in 1975, 4-5 years after it was withdrawn in other countries.

Why is the UK always so late to act on medicine harm?

You may say “that was 50 years ago”, things have changed, but MHRA’s lack of action on AstraZeneca covid vaccines resulted in patient deaths as recently as 2021. If anything, the MHRA’s recent transformation from “From watchdog to regulator” (as proclaimed by June Raine) is making things worse. As was pointed out several times during the debate, Primodos was 40 times the strength of the contraceptive pill, this is a risk a lay person can understand, why didn’t the regulator?

Sir Jacob Rees-Mogg stated “The drug was used in South Korea and Germany as an abortifacient. It was used to procure abortions.” Why would MHRA allow a drug that is used overseas for abortions, as a pregnancy test? It would be reasonable to assume there could be a risk of miscarriage. Why did MHRA reject Professor Carl Heneghan’s (director of the Centre for Evidence-Based Medicine at Oxford University) report showing “a clear association” between Primodos and several forms of malformation? Why hasn’t MHRA taken the actions recommended by the Cumberlege report? The yellowcard system is clearly not fit for purpose and is resulting in unnecessary harm to patients.

The Perseus Group believes that a large part of the problem is that medicine safety doesn’t follow the best practice safety management practices of other safety critical sectors like aviation or nuclear. For example, MHRA does not set safety thresholds for the number of deaths/injuries which is allowed before a medicine is suspended. Previous Inquiries, such as the Cumberlege Inquiry, do little or nothing to improve the fundamentals of MHRA’s safety management because there is no input from those involved in managing safety in other safety critical sectors.

The Government committed to take action on Primodos after the Cumberlege report (if fact Primodos was a key driver resulting in the commissioning of the report), but they have limited that action to pelvic mesh and Valproate. The Patient Safety Commissioner role was created to close the gap but again her scope has been limited to mesh and Valproate. Primodos families have been fighting for decades for redress but the system is against them, they have been failed by the Government, the legal system and the regulator.

There are dozens of medicine and medical device victim groups (antidepressants, morning sickness medicines, vaccines etc) fighting their own battles for justice, what is the underlying theme?

A regulator failing to do their duty to keep people safe, influenced by pharmaceutical companies and defended by the Government.

Esther McVey stated “Sadly, Primodos is not an isolated case, and we have seen many examples over the years of our regulatory bodies failing to keep patients safe from new medicines and medical devices. In 2013, the Medicines and Healthcare products Regulatory Agency listed 27 medicines that had been withdrawn on safety grounds. The average time they were on the market was 11 years. I wonder how many times we will allow history to repeat itself. There have been reports and reviews calling for reform, and back in 2004 the Health Committee undertook an inquiry into the influence of the pharmaceutical industry. It noted, of drug companies, the ‘closeness that has developed between regulators and companies’”

Of MRHA’s 16 board members, 6 have Declarations of Interest relating to healthcare companies including pharmaceutical giants such as Sanofi, AstraZeneca and Pfizer. Pharmaceutical companies have been given immunity for several medicines by the Government, incentivizing them to support the pharmaceutical companies position rather than the victims. Pharmaceutical companies already have deep pockets, why are the Government willing to support them rather than those harmed?

Sitting from the outside, I see many victim groups fighting their individual battles in silos. Imagine their power if they all came together as a single voice demanding reform of MHRA? 22 MPs spoke in the Primodos debate, every single one of them wanting justice for the victims. The Parliamentary Under-Secretary of State for Health and Social Care Maria Caulfield has agreed to meet with families and review the findings of the Cumberlege report, so this looks like a small step forwards for this group or at least a little more hope.

Do we now have the critical mass to demand reform of MHRA? If everyone came together, could we get a regulator that prioritises patient safety over pharmaceutical company profits?

Will the media start joining the dots?

October 6, 2023 Posted by | Science and Pseudo-Science, Timeless or most popular | , | Leave a comment