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CDC IN HOT SEAT OVER SKEWED COVID DATA

The Highwire with Del Bigtree | February 1, 2024

During COVID, the public was fed fearful numbers showing exaggerated death rates in unvaccinated populations. Where did they get this data and how accurate was it?

February 2, 2024 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, Video, War Crimes | , | Leave a comment

Medicine Has Been Fully Militarized

By Clayton J. Baker, MD | Brownstone Institute | January 30, 2024

I am thinking of a certain industry. See if you can guess what it is.

This industry is huge, constituting a large portion of the nation’s GDP. Millions of people earn their living through it, directly or indirectly. The people at the top of this industry (who operate mostly behind the scenes, of course) are among the super-rich. This industry’s corporations lobby the nation’s government relentlessly, to the tune of billions of dollars per year, both to secure lucrative contracts and to influence national policy in their favor. This investment pays off richly, sometimes reaching trillions of dollars.

The corporations supplying this industry with its materiel conduct advanced, highly technical research that is far beyond the understanding of the average citizen. The citizens fund this research, however, through tax dollars. Unbeknownst to them, many of the profits gained from the products developed using tax dollars are kept by the corporations’ executives and investors.

This industry addresses fundamental, life-or-death issues facing the nation. As such, it relentlessly promotes itself as a global force for good, claiming to protect and save countless lives. However, it kills a lot of people too, and the balance is not always a favorable one.

The operational side of this industry is emphatically top-down in its structure and function. Those who work at the ground level must undergo rigorous training that standardizes their attitudes and behavior. They must follow strict codes of practice, and they are subject to harsh professional discipline if they deviate from accepted policies and procedures, or even if they publicly question them.

Finally, these ground-level personnel are handled in a peculiar manner. Publicly, they are frequently lauded as heroes, particularly under declared periods of crisis. Privately, they are kept completely in the dark regarding high-level industry decisions, and they are often lied to outright by those at higher levels of command. The “grunts” even significantly forfeit some fundamental civil liberties for the privilege of working in the industry.

What industry am I describing?

If you answered, “the military,” of course you would be correct. However, if you answered “the medical industry,” you would be every bit as right.

In President Eisenhower’s farewell speech of January 17, 1961, he stated that “…in the councils of government, we must guard against the acquisition of unwarranted influence, whether sought or unsought, by the military-industrial complex.” Sixty-three years on, many Americans understand what he was referring to.

They see the endless cycle of undeclared wars and decades-long foreign occupations that are undertaken on nebulous or even outright false pretenses. They see the ever-hungry mega-industry that produces super-expensive, high-tech killing devices of every imaginable form, as well as the steady stream of traumatized soldiers that it spits out. War (or, if you prefer its Orwellian nickname, “defense”) is big business. And as Eisenhower warned, as long as those profiting from it drive the policy and the money stream, it will not only continue, it will continue to grow.

Other mega-industries – the medical industry in particular – have generally fared better in public perception than the military-industrial complex. Then came Covid.

Among its many harsh lessons, Covid has taught us this: if you substitute Pfizer and Moderna for Raytheon and Lockheed Martin, and swap the NIH and CDC for the Pentagon, you get the same result. The “medical-industrial complex” is every bit as real as its military-industrial counterpart, and it is every bit as real a problem.

As a physician, I am embarrassed to admit that until Covid, I possessed only an inkling that this was so – or more accurately, I knew it, but didn’t realize how bad it was, and I didn’t worry about it too much. Sure (I thought), Pharma engaged in dishonest practices, but we’d known that for decades, and after all, they do make some effective drugs. Yes, physicians were increasingly becoming employees, and protocols were dictating care more and more, but the profession still seemed manageable. True, healthcare was far too expensive (gobbling up a reported 18.3 percent of the US GDP in 2021), but healthcare is inherently expensive. And after all, we’re saving lives.

Until we weren’t.

By early-to-mid 2020, it became obvious to those paying attention that the Covid “response,” while promoted as a medical initiative, was in fact a military operation. Martial law had effectively been declared approximately on the Ides of March 2020, after President Trump was mysteriously convinced to cede the Covid response (and practically speaking, control of the nation) to the National Security Council. Civil liberties – freedom of assembly, worship, the right to travel, to earn one’s living, to pursue one’s education, to obtain legal relief – were rendered null and void.

Top-down diktats on how to manage Covid patients were handed down to physicians from high above, and these were enforced with a militaristic rigidity unseen in doctors’ professional lifetimes. The mandated protocols made no sense. They ignored fundamental tenets of both sound medical practice and medical ethics. They shamelessly lied about well-known, tried-and-true medicines that were known to be safe and appeared to work. The protocols killed people.

Those physicians and other professionals who spoke out were effectively court-martialed. State medical boards, specialty certification boards, and large healthcare system employers virtually tripped over each other in the rush to delicense, decertify, and fire dissenters. Genuine, courageous physicians who actually treat patients, such as Peter McCullough, Mary Talley Bowden, Scott Jensen, Simone Gold, and others, were persecuted, while non-practicing bureaucrats like Anthony Fauci were hailed with false titles like “America’s Top Doctor.” The propaganda was as nauseating as it was blatant. And then came the jabs.

How did this happen to medicine?

It all seemed so sudden, but in fact it has been in the works for years.

Covid taught us (by the way, Covid has been such a harsh tutor, but haven’t we learned so much from her!) that the medical-industrial complex and military-industrial complex are deeply connected. They are not just twins, or even identical twins. They are conjoined twins, and so-called “Public Health” is the tissue shared between them.

The SARS CoV-2 virus, after all, is a bioweapon, developed over a period of years, funded by US tax dollars in a joint effort between Fauci’s NIH and the Department of Defense to genetically manipulate the transmissibility and virulence of coronaviruses (all done in the name of “Public Health,” of course).

Once the bioweapon was out of the lab and into the population, the race was on within the medical-industrial complex to develop and market the supremely profitable antidote to the bioweapon. Cue the full-on military takeover of medicine: the martial law lockdowns, the suppression of cheap and effective treatments, the persecution of dissidents, the ceaseless propaganda and anti-science, and the unabashed whoring of most hospital systems for CARES Act money.

We know the rest. The ill-conceived, toxic, gene-therapy antidote, falsely billed as a “vaccine,” was foisted upon the population by blackmail (“the vaccine is how we end the pandemic”), the effective bribery of medical authorities and politicians, as well as other Deep-State directed psyops designed to divide the population and scapegoat dissenters (“pandemic of the unvaccinated”).

The end result even sounds like the aftermath of a gigantic military operation. Millions are dead, many millions more are psychologically traumatized, economies are in tatters, and a few warmongers are fantastically rich. Moderna CEO Stephane Bancel (who, incidentally, oversaw the construction of the Wuhan Institute of Virology years ago) is a freshly minted billionaire. And not one of those who caused all the mischief are in prison.

At this writing, virtually all the major healthcare systems, specialty regulatory boards, specialty associations, and medical schools are standing at attention, still in lockstep with the received – and by now, clearly false – narrative. Their funding, after all, be it from Pharma or the Government, depends upon their obedience. Barring dramatic change, they will respond in the same fashion when orders come down from above in the future. Medicine has been fully militarized.

In his farewell address, Eisenhower said something else that I believe is most prescient here. He described that a military-industrial complex fostered “a recurring temptation to feel that some spectacular and costly action could become the miraculous solution to all current difficulties.”

Enter Disease X.

C.J. Baker, M.D. is an internal medicine physician with a quarter century in clinical practice. He has held numerous academic medical appointments, and his work has appeared in many journals, including the Journal of the American Medical Association and the New England Journal of Medicine. From 2012 to 2018 he was Clinical Associate Professor of Medical Humanities and Bioethics at the University of Rochester.

January 31, 2024 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | , , | Leave a comment

Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule

By Brenda Baletti, Ph.D. | The Defender | January 29, 2024

Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science.

Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review.

The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule.

After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail.

Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs).

Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials.

They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.”

They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters.

“It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote.

Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies.

It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender.

“Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added.

According to McCollough, “mRNA should never have been authorized for human use.”

Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.”

Here are six takeaways from the review:

1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner

Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years.

To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote.

The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease.

However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines.

There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction.

The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself.

The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.”

The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added.

2. Steps were taken in trials to overestimate vaccine efficacy 

Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do.

“No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote.

Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.”

Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19.

There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%.

The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety.

Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote.

Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine.

The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate.

One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large.

According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility.

While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively.

“A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote.

As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death.

However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote.

And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.”

They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19.

One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19.

A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues.

3. The trials underestimated the adverse events, including death, despite evidence in the data. 

Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here.

First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group.

“Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked.

Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population.

None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote.

Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended.

During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data.

And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports.

Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.”

In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.”

This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.”

4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary.

Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population.

The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants.

Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.”

After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke.

And millions of AEs have been reported to those systems.

Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system.

In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervousimmune, reproductive and other systems.

The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious.

In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal.

“The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.”

5. The failure to appropriately test for safety and toxicity poses serious problems. 

Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs.

Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues.

That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids.

Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown.

McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns.

Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time

This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown.

6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness.

The review points readers to a series of papyrus that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines.

“The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection.

They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself.

They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants.


Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.

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.

January 30, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular | | Leave a comment

2024 election candidates join thousands of doctors in opposing dangerous COVID shots

‘Many are also pledging not to take donations from Big Pharma’

By Calvin Freiburger | Life Site News | January 29, 2024

More than 100 candidates for public office and nearly as many current officeholders across 35 states have publicly declared that they believe the COVID-19 vaccines should be “immediately discontinued” in the interest of public safety, according to a group of medical freedom advocates.

Dr. Mary Talley Bowden, an otolaryngology and sleep medicine specialist who is also president of the group Americans for Health Freedom (AHF), announced Sunday that the tally of public figures who have signed their COVID declaration is up to “106 candidates, 103 elected officials and 1 Surgeon General [Dr. Joseph Ladapo of Florida] from 35 states.”

“Many are also pledging not to take donations from Big Pharma,” she added. “Over 17,000 physicians stand behind them.”

She shared the list of the newest signatories in her announcement post on X (Twitter). Most were state-level candidates, though three are currently running for Congress.

The complete list of signatories can be found at AHF’s website, which also contains the declaration itself.

“We declare, and the data confirms that COVID-19 experimental genetic therapy injections must end,” it reads. “All COVID-19 and other modified mRNA ‘vaccines’ must be immediately discontinued. We demand that Covid-19 vaccines be removed from the pediatric vaccine schedule […] We declare injury from COVID-19 ‘vaccines’ must be recognized. Compensation must be provided for those injured by these injections. Funding must be allocated to the study of these syndromes and the development of diagnostics and treatments should be pursued.”

“We declare Pfizer, Moderna, BioNTech, Janssen, Astra Zeneca studies were severely flawed, and they withheld safety and efficacy information from patients and physicians. They should face legal consequences for their dereliction of scientific duty which resulted in countless unnecessary disability and deaths,” the declaration also says. “We declare governments, media, global regulatory bodies, and medical agencies, such as CDC, FDA, NIH, NIAID, MHRA, NHS, TGA, SAPRA etc., and unelected international bodies including but not limited to WHO, WEF, UN, GAVI, and EcoHealth Alliance must be held accountable for mandating policies and procedures, and directing funding for reckless gain of function research that resulted in massive harms.”

The public health establishment has been overwhelmingly averse to investigating problems with the mRNA-based COVID vaccines from Pfizer and Moderna, which were developed and reviewed in a fraction of the time vaccines usually take under former President (and likely 2024 Republican presidential nominee) Donald Trump’s Operation Warp Speed initiative, yet concerns persist thanks to a large body of evidence affirming they carry significant health risks.

The federal Vaccine Adverse Event Reporting System (VAERS) reports 36,986 deaths, 213,536 hospitalizations, 21,335 heart attacks, and 28,052 myocarditis and pericarditis cases as of December 29, among other ailments. An April 2022 study out of Israel indicates that COVID infection itself cannot fully account for the myocarditis numbers despite common insistence to the contrary.

Jab defenders are quick to stress that reports submitted to VAERS are unconfirmed, as anyone can submit one, but U.S. Centers for Disease Control and Prevention (CDC) researchers have recognized a “high verification rate of reports of myocarditis to VAERS after mRNA-based COVID-19 vaccination,” leading to the conclusion that “under-reporting is more likely” than over-reporting.

2010 report submitted to the U.S. Department of Health & Human Services’ (HHS’s) Agency for Healthcare Research and Quality (AHRQ) warned that VAERS caught “fewer than 1% of vaccine adverse events.” On the problem of under-reporting, the VAERS website offers only that “more serious and unexpected medical events are probably more likely to be reported than minor ones” (emphasis added).

In 2021, Project Veritas shed light on some of the reasons for such under-reporting with undercover video from inside Phoenix Indian Medical Center, a facility run under HHS’s Indian Health Service program in which emergency room physician Dr. Maria Gonzales laments that myocarditis cases go unreported “because they want to shove it under the mat,” and nurse Deanna Paris attests to seeing “a lot” of people who “got sick from the side effects” of the COVID shots, but “nobody” is reporting them to VAERS “because it takes over a half hour to write the damn thing.”

Further, VAERS is not the only data source containing red flags. Data from the Pentagon’s Defense Medical Epidemiology Database (DMED) shows that 2021 saw drastic spikes in a variety of diagnoses for serious medical issues over the previous five-year average, including hypertension (2,181%), neurological disorders (1,048%), multiple sclerosis (680%), Guillain-Barre syndrome (551%), breast cancer, (487%), female infertility (472%), pulmonary embolism (468%), migraines (452%), ovarian dysfunction (437%), testicular cancer (369%), and tachycardia (302%).

Leading COVID shot manufacturer Pfizer donated more than $8.5 million to political candidates, leadership PACs, trade associations, and party committees representing both parties in 2022, fueling suspicion as to why only a handful of nationally prominent GOP officeholders, such as U.S. Sen. Ron Johnson of Wisconsin and Gov. Ron DeSantis of Florida, are opposed to the company’s vaccine.

January 30, 2024 Posted by | Civil Liberties, Corruption, Deception, Timeless or most popular, War Crimes | , | Leave a comment

Dr. Mark Trozzi’s Licence Stripped for “Misinformation” & Criticizing CPSO Policy

Dr. Trozzi to appeal after College of Physicians and Surgeons of Ontario revokes his licence

PRESS RELEASE | January 25, 2024

The Ontario Physicians and Surgeons Discipline Tribunal issued a penalty decision today revoking Dr. Mark’s Trozzi‘s medical licence after ruling in October that he had committed acts of professional misconduct by spreading misinformation about Covid-19 science and making statements critical of Covid-19 public health policies and recommendations. Through his counsel, Michael Alexander, Dr. Trozzi announced today that he will exercise his statutory right to appeal the decision to the Ontario Divisional Court.

In reaching its decision, the Tribunal rejected Supreme Court cases, dating from 1939, which hold that Canadians enjoy an absolute constitutional right to express minority opinions on any subject. This allowed the Tribunal to rule that the College has a right to regulate the expression of its members in the name of the public interest.

The Tribunal’s ruling also rested on the prior discipline hearing decision, where the Tribunal found that Dr. Trozzi had caused harm by spreading misinformation, even though expert witnesses for the College failed to tender evidence that Dr. Trozzi’s statements had caused harm to a patient or a member of the public.

In support of its ruling, the Tribunal also rejected a 41-page report Dr. Trozzi submitted in 2021 in which he defended himself against the College’s initial allegations, citing 29 references from mainstream sources such as Lancet, the New England Journal of Medicine, Public Health Ontario and Statistics Canada. This was done without mentioning that the College’s main expert witness, Dr. Andrew Gardam, had admitted on cross-examination during the discipline hearing that he had never attempted to refute the Trozzi report.

When the pandemic was on the horizon in 2020, Dr. Trozzi, a university professor and 25-year ER veteran, played a leading role in preparing his own ER facility to deal with Covid patients. However, while the press was reporting in late 2020 that ER rooms were overwhelmed, Dr. Trozzi’s ER room was virtually empty. Wondering how this could be, Dr. Trozzi called colleagues around Canada and the U.S. to inquire about their experiences and learned that their ER rooms were empty too.

As a result, Dr. Trozzi began to study Covid-19 science rigorously and soon discovered the government’s narrative regarding the virus was deeply flawed. He then quit his job and devoted himself full-time to exploring the truth about all things Covid on a dedicated site. When a scientist friendly to the government’s narrative alerted the College of Physicians to the site and Dr. Trozzi’s heretical views, the College launched an investigation that resulted in his prosecution for professional misconduct.

Dr. Trozzi’s registration history: no disciplinary issues in 20+ years of medicine since his start Jun. 22, 1990. Issues only began when he, like any other doctors during Covid, spoke out against the unscientific Covid and “vaccine” mandates and, ironically, by continuing to follow the CPSO’s own guidelines prior to Covid, including giving patients informed consent for any medical treatments.

Alexander commented: “Since Dr. Trozzi’s right to appeal to the Divisional Court is based on a statute, the Court will be required to employ the highest standard of review on all legal issues, and that standard is correctness. In other words, the Court will have to determine whether the Tribunal got the right answer on every key legal issue; and where it does not, the Court will be required to correct the Tribunal’s reasoning. The College has never had to face a fundamental challenge to its authority on this basis.”

He added: “On correctness review, it will be very hard for the College to justify its initial decision to investigate Dr. Trozzi. Under the legislation, the College must have reasonable and probable grounds, which is the criminal standard, for believing that a member has committed an offence before it can launch an investigation. However, in its orders, the College did not describe any evidence to support the probable belief that Dr. Trozzi had done something wrong, and even failed to cite a specific offence. The appeal should succeed on this point alone.”

Finally: “The Court of Appeal’s recent decision to refuse to hear Jordan Peterson’s case does not mean, as some have speculated, that freedom of expression is dead in Ontario. The Peterson case turned on the issue of whether the College of Psychologists could regulate the form of Dr. Peterson’s expression, not its content. In Trozzi, the Divisional Court must decide whether to recognize the right of every citizen to express an alternative opinion, even if it offends censorious bureaucrats.”

To support Dr. Trozzi, DONATE HERE.

January 28, 2024 Posted by | Civil Liberties, Deception, Full Spectrum Dominance, Science and Pseudo-Science | , , , | 1 Comment

‘Plagues, Cyborgs, and Supersoldiers’: Report Suggests Pentagon Exploring Biotech-Based Warfare

By Brenda Baletti, Ph.D. | The Defender | January 26, 2024

The Pentagon is exploring how new biotechnological innovations — including mRNA vaccines, CRISPR gene-editing and brain-computer interfaces (BCI) — could change the nature of future warfare, investigative journalist Lee Fang reported Thursday.

The U.S. Department of Defense (DOD) used to consider biotech-based warfare too risky or even eugenicist, according to a new report produced for the agency by the RAND Corporation. But recent advances “change strategic choices for the human body as a warfighting domain,” the authors of the report wrote.

The RAND Corporation is a military think tank established during the Cold War and known for its work actively influencing government and military policy.

The report — “Plagues, Cyborgs, and Supersoldiers: The Human Domain of War” — presents a series of future war scenarios based on advances in engineered bioweapons, the Internet of Bodies and genomics that the authors said “might seem fantastical,” but are “not far-fetched,” given rapid advances in 21st-century biotechnology.

The report recommends that military planning anticipate these future war scenarios.

“We see a complex, high-threat landscape emerging where future wars are fought with humans controlling hyper-sophisticated machines with their thoughts,” where “synthetically generated, genomically targeted plagues” disrupt the American military-industrial base and the future soldier is an “enhanced warfighter” who can survive in extreme conditions, the report warns.

Fang told The Defender, “These Pentagon research reports read like science fiction, but they provide crucial insight into how the military sees future conflict and exerts pressure on lawmakers on crucial policy issues.”

The scenarios: engineered pathogens, Internet of Bodies and enhanced genomics

The report posits scenarios with future COVID-19-like pandemics that emerge from engineered pathogens, and considers them in the context of war with China and Russia.

The authors argue the U.S. would be at a major disadvantage without serious prior investment in its own biotech weapons and a strategy to curb the development of such weapons by competing global powers.

The first hypothetical scenario, referred to as a “vignette” in the report, takes place in 2028, when a new and highly infectious “SARS-CoV-3” spreads in the South China Sea and then on U.S. Navy vessels, forcing them to cease operations. U.S. agencies get caught up in infighting over which agency should investigate the causes and spearhead the response.

China, which appears to be immune to the virus, launches an assault on Taiwan, and the disabled U.S. fleet is unable to respond.

The World Health Organization credits Chinese social distancing with its slow spread, unaware that the Chinese military and population were unwittingly vaccinated against the new version of the disease, released as a bioweapon.

This scenario was initially conceived by Pentagon researchers, Fang wrote, who “believe that a ‘coronavirus bioweapon’ may lurk on the horizon.”

In another scenario — “Pandemic Geopolitics” — a new airborne pathogen with a long contagious period and an astronomical mortality rate of 2.5% begins circulating in 2033, killing 1 million Americans in four months with 6.5 more million projected to die.

China and Russia in this scenario have vaccines in advance and use the opportunity to expand their borders. The U.S. and Europe lack the capacity for a military response.

The report then turns to an Internet of Bodies scenario that Fang wrote is “seemingly inspired by the decline of Sen. Dianne Feinstein,” and set in a more distant future.

Elderly congressional leaders fear a loss of power due to rumors of their cognitive decline. To appear more competent, they have BCI devices implanted in their brains to boost their physical and cognitive functioning. However, the devices malfunction, the politicians act erratically and foreign allies begin to distance themselves from the U.S.

In yet another scenario, government employees use artificial lenses for their eyes that have recording devices and storage. However, the technology also is used to collect and leak sensitive information, unbeknownst to the U.S. government.

BCI could offer benefits to the “warfighter,” for example allowing commanders and their forces to communicate directly. However, the report cautions that BCI devices can also be hacked.

The U.S. currently leads Internet of Bodies technology development, at least according to the number of patents that have been filed, but the authors warned that “China is quickly catching up.”

The authors posit a distant future where genomic surveillance is used to select the most appropriate military recruits and another where genetic modifications are used to create “super soldiers.”

U.S. should plan to integrate biological warfighting

The report makes recommendations inspired by missteps the authors see regarding the handling of the COVID-19 response, and advises the Pentagon to consider the risks and benefits of emerging technologies.

Fang wrote:

“In a not-so-veiled shot at those who denied the COVID-19 lab leak theory as ‘disinformation,’ they note that in the event of an engineered coronavirus bioweapon, most scientists ‘would likely’ presume that the virus had a natural or zoonotic origin, disputing claims of a manufactured attack. This ‘ambiguity could serve a nation-state well,’ the report argues.”

The existing United Nations Biological Weapons Convention should be revised to address new issues raised by new technologies, the authors recommend. But they also called such treaties “intractable” — because some countries don’t comply — and recommended “bilateral treaties” governing bioweapons.

They also call for the U.S. to divest from the Wuhan Institute of Virology, which many argue is the source of the COVID-19 lab leak.

According to Fang, “The report takes aim at Congress, criticizing the recent repeal of the COVID-19 vaccine mandate for service members. It urges lawmakers to resist ‘anti-vaccine populism’ to ensure military readiness.”

The authors recommended sanctions on foreign powers misusing biotechnology and that the Pentagon begin using genetic screening.

Finally, they said the DOD should develop guidelines for integrating biological warfighting into its suite of military capabilities.

Despite the science fiction-esque nature of the scenarios RAND poses in the report, Fang said it is important to track such policy documents, because similar past reports have foreshadowed future government action that did come to pass.

He wrote:

“Over a decade ago, In-Q-Tel, the venture capital arm of the CIA, published a report looking at the opportunities posed by social media and suggested that major platforms could be analyzed with artificial intelligence for sentiment analysis and advanced intelligence gathering.

“Soon after, the agency began funding several specialized startups to analyze protests and political movements using platforms such as Twitter and Facebook. Some of the CIA-backed firms have gone on to engage in sophisticated forms of surveillance.”


Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.

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.

January 27, 2024 Posted by | Militarism, Timeless or most popular, War Crimes | , , | Leave a comment

Federal Court Judge Pulls Canada Back from the Brink

By Bruce Pardy | Brownstone Institute | January 25, 2024

The Canadian government’s use of the Emergencies Act was unlawful. The Trucker Convoy did not constitute a national emergency. So said a judge of the Federal Court on Tuesday. The decision may help to pull Canada back from the brink of authoritarian rule.

The Federal Court decision contains four conclusions. Two prerequisites for invoking the Emergencies Act, said Justice Richard Mosley, were not met. Moreover, the two regulations issued under it were unconstitutional. Predictably, the government has promised to appeal. For the government to prevail, an appeal panel would have to overturn all four. But there is a wrinkle, which I will get to momentarily.

Between 1963 and 1970, the Front de libération du Québec (FLQ), a separatist organization in Quebec, committed bombings, robberies, and killed several people. In October 1970, they kidnapped British trade commissioner James Cross, and then kidnapped and killed Pierre Laporte, a minister in the Quebec government. In response, Pierre Trudeau’s government invoked the War Measures Act, the only time it had been used in peacetime. In the years that followed, the invocation of the Act became regarded as a dangerous overreach of government powers and breach of civil liberties.

The Emergencies Act, enacted in 1988 to replace the War Measures Act, had higher thresholds. It was supposed to be more difficult for governments to trigger. Before Covid and the trucker convoy, it had never been used.

The Freedom Convoy arrived at Parliament Hill in Ottawa on January 29, 2022 to protest Covid vaccine mandates. The truckers parked unlawfully in downtown Ottawa. They violated parking bylaws and probably the Highway Traffic Act. Authorities could have issued tickets and towed the trucks away. But they didn’t.

In the meantime, protests in other parts of the country emerged. Trucks blocked border crossings in Coutts, Alberta and at the Ambassador Bridge in Windsor, Ontario. Local and provincial law enforcement dealt with those protests and cleared the borders. By February 15, when Justin Trudeau’s government declared a public order emergency and invoked the Emergencies Act, only the Ottawa protests had not been resolved.

The government issued two regulations under the Act. One prohibited public assemblies “that may reasonably be expected to lead to a breach of the peace.” The other outlawed donations and authorized banks to freeze donors’ bank accounts. On February 18 and 19, police brandishing riot batons descended on the crowd. They arrested close to 200 people, broke truck windows, and unleashed the occasional burst of pepper spray. By the evening of the 19th, they had cleared the trucker encampment away. Banks froze the accounts and credit cards of hundreds of supporters. On February 23, the government revoked the regulations and use of the Act.

Governments cannot use the Emergencies Act unless its prerequisites are met. A public order emergency must be a “national emergency” and a “threat to the security of Canada,” both of which are defined in the Act. A national emergency exists only if the situation “cannot be effectively dealt with under any other law of Canada.” “Threats to the security of Canada” can be one of several things. The government relied upon the clause that requires activities “directed toward or in support of the threat or use of acts of serious violence against persons or property for the purpose of achieving a political, religious or ideological objective.”

The trucker protests were neither a national emergency, Mosley concluded, nor a threat to the security of Canada.

There was no national emergency:

Due to its nature and to the broad powers it grants the Federal Executive, the Emergencies Act is a tool of last resort. [Cabinet] cannot invoke the Emergencies Act because it is convenient, or because it may work better than other tools at their disposal or available to the provinces.…in this instance, the evidence is clear that the majority of the provinces were able to deal with the situation using other federal law, such as the Criminal Code, and their own legislation…For these reasons, I conclude that there was no national emergency justifying the invocation of the Emergencies Act and the decision to do so was therefore unreasonable and ultra vires.

A threat to the security of Canada did not exist:

Ottawa was unique in the sense that it is clear that [Ottawa Police Services] had been unable to enforce the rule of law in the downtown core, at least in part, due to the volume of protesters and vehicles. The harassment of residents, workers and business owners in downtown Ottawa and the general infringement of the right to peaceful enjoyment of public spaces there, while highly objectionable, did not amount to serious violence or threats of serious violence…[Cabinet] did not have reasonable grounds to believe that a threat to national security existed within the meaning of the Act and the decision was ultra vires.

Nor were the regulations constitutional. The prohibition on public assemblies infringed freedom of expression under section 2(b) of the Charter of Rights and Freedoms. Empowering financing institutions to provide personal financial information to the government and to freeze bank accounts and credit cards was an unconstitutional search and seizure under section 8. Neither was justified, Mosley concluded, under section 1 of the Charter, the “reasonable limits” clause.

To prevail on appeal, the government would have to reverse all four conclusions. Justice Mosley did not make obvious errors of law. But there are a couple of odd bits. In particular, Mosley admits to doubts about how he would have proceeded had he been at the cabinet table himself:

I had and continue to have considerable sympathy for those in government who were confronted with this situation. Had I been at their tables at that time, I may have agreed that it was necessary to invoke the Act. And I acknowledge that in conducting judicial review of that decision, I am revisiting that time with the benefit of hindsight and a more extensive record of the facts and law…

Which brings us to the wrinkle. In April 2022, Richard Wagner, the Chief Justice of the Supreme Court of Canada, gave an interview to Le Devoir. Speaking in French, he characterized the protest on Wellington Street in Ottawa, where Parliament and the Supreme Court are located, as “the beginning of anarchy where some people have decided to take other citizens hostage.” Wagner said that “forced blows against the state, justice and democratic institutions like the one delivered by protesters… should be denounced with force by all figures of power in the country.” He did not mention the Emergencies Act by name. But his comments could be interpreted as endorsing its use.

The government’s appeal will go first to the Federal Court of Appeal but then to the Supreme Court of Canada. Its chief justice appears to have already formed an opinion about the dispute. Having made his public comments, the chief justice should announce that he will recuse himself from the case to avoid a reasonable perception of bias. That too would help bring Canada back from the brink.

Bruce Pardy is executive director of Rights Probe and professor of law at Queen’s University.

January 26, 2024 Posted by | Civil Liberties, Full Spectrum Dominance, War Crimes | , , | 1 Comment

The DOJ Quietly Prosecutes the Covid Resistance

Brownstone Institute | January 24, 2024

Midwives in New York and plastic surgeons in Utah didn’t close schools, shutter businesses, or add trillions of dollars to the national debt, yet they are the primary targets of the Biden DOJ’s Covid prosecution.

Court documents reveal how the Department of Justice has dedicated hundreds of thousands of dollars in resources to prosecuting Americans who forged Covid vaccination statuses, according to a new report from David Zweig.

The feds have used undercover agents to take down midwives and local doctors who forged vaccine cards. Many of the “criminals” had no profit motive; they objected to the mandates based on ideological principles or medical concerns, and they needed cards to participate in society.

Zweig highlights cases that have been brought as late as spring 2022, “long after it was widely known that the vaccines did not stop infection or transmission, which was the only ethical and logistical justification for mandates.”

More than ever, it is clear that the calls to “move on” from Covid are reserved for protecting those who implemented tyranny.

Politicians like Gavin Newsom, who celebrated their acquisition of dictatorial powers in 2020, demand forgiveness for eviscerating the Bill of Rights. In the Atlantic, Professor Emily Oster called for a “pandemic amnesty” after advocating for vaccine mandates for employees and students, school closures, “full lockdowns” over the holidays, and universal masking. “Let’s focus on the future,” she insists.

The Biden White House has largely adapted this strategy; substituting foreign conflicts as its new justifications for exorbitant foreign spending and widespread domestic censorship.

With the presumptive nomination of President Trump in the Republican Party, citizens’ hope for answers on the Covid response hinges on Robert Kennedy, Jr.’s participation in the presidential debates. Both parties will work to ensure that does not happen.

In effect, the powerful have already enjoyed a pandemic amnesty. Politicians have not lost their power nor faced a serious inquiry into their malfeasance. Pharmaceutical companies received government-sponsored immunity from lawsuits while pocketing billions of dollars from federal, state, and local mandates. The apparati behind the Covid response remain intact with little threat to their continued acquisition of power.

But the “focus on the future” does not extend to those who resisted the Covid hegemon. “The mandates were so feared and loathed by significant and diverse numbers of citizens that they were willing to become criminals rather than comply,” Zweig explains.

The Biden Department of Justice will not give dissidents the courtesy of a pandemic amnesty. Instead, the targets of the regime will join the ranks of Americans punished by the Department of Justice for their resistance while nondescript bureaucratic tyrants continue their careers unscathed.

The damage to the nation, however, cannot be glossed over. Learning loss, business closures, vaccine injuries, the erosion of trust in all major institutions, trillions of dollars added to the national debt, trillions more in collateral damage, and the institution of a censorship state will take decades to fix, if possible at all.

But there is no indication that the powerful will be held accountable for the damage they imposed. Instead, the Biden Administration has decided to target citizens who resisted its irrational edicts. The same edicts for which they insist they must be granted an “amnesty.” Such actions only increase the devastation from a disastrous policy response.

January 25, 2024 Posted by | Civil Liberties | , , , | Leave a comment

CHD, Parents Take on Philadelphia Health Officials in Bid to Overturn Law Allowing Kids to Get Vaccines Without Parents’ Consent

By Brenda Baletti, Ph.D.| The Defender | January 23, 2024

Children’s Health Defense (CHD) and seven Pennsylvania parents last week opposed the City of Philadelphia’s motion to dismiss their lawsuit seeking to overturn the city’s law that allows minors as young as 11 to consent to vaccination without their parents’ knowledge.

Tricia Lindsay, lead attorney for the plaintiffs, told The Defender it is important the case be heard and that its significance goes beyond the City of Philadelphia.

“This case is one which addresses pivotal issues, and is significant for all citizens,” Lindsay said, adding, “The right of a parent to the care, custody and control of their children is not a right which should be taken lightly, and is not one that can simply be extinguished with the stroke of a pen.”

The lawsuit, filed Nov. 1, 2023, alleges the City of Philadelphia engaged in a “wink and a nod” practice of vaccinating children behind parents’ backs without informed consent for the past 15 years, under the cover of its 2007 General Minor Consent Regulation (MCR).

That rule allows children 11 and older to consent to vaccination without parental knowledge as long as they receive a “vaccine information statement” for the administered shot.

It also absolves the vaccine administrator of liability related to the vaccine if the minor gives consent.

On May 14, 2021, the Philadelphia Department of Public Health enacted an additional COVID-19 Minor Consent Regulation, allowing children ages 11 and up to consent to the COVID-19 vaccine then available under emergency use authorization.

In its motion to dismiss, filed on Jan. 5, the city and its health department argued that none of the plaintiffs had been directly harmed or are likely to be harmed by the regulations and therefore they lack standing to sue.

City and health officials also argued that even if the plaintiffs did have standing, the complaint failed to “state a claim,” or show sufficient facts and legal justification, that Philadeliphia’s law violated federal or state law or that it violated parents’ constitutional rights to make decisions about their children’s upbringing.

But the defendants ignored a key relevant federal court decision — Booth v. Bowser — cited by the plaintiffs to support their claim and which legally “eviscerates” the regulations, CHD told the court.

Plaintiffs in Booth v. Bowser sought to stop the D.C. Minor Consent for Vaccinations Amendment Act of 2020, a bill that similarly would have allowed children as young as 11 in the District of Columbia to be vaccinated without the knowledge or consent of their parents. Defendants in that case tried to have the case thrown out using the same rationale invoked by Philadelphia plaintiffs — lack of standing and failure to state a claim.

In Booth v. Bowser, the court found the plaintiffs did have standing, had adequately pleaded their claims and were likely to win their case. When the amended version of the bill —  Consent for Vaccinations of Minors Amendment Act of 2022 — took effect March 10, 2023, the section allowing children under age 11 to consent to vaccines without their parents’ knowledge had been repealed.

But in the Philadelphia case, rather than following that precedent and repealing the regulations, CHD attorneys wrote:

“Defendants here refuse to acknowledge that children, particularly those as young as eleven, are simply incapable of making vaccination decisions on their own, especially when defendants engage in manipulative tactics directly targeting children with false statements of safety and efficacy, calculated bullying, and peer pressure campaigns.

“Defendants have the audacity to say they are not actively interfering in compelling children to be vaccinated without parental knowledge and consent when they are blatantly manipulating children to the point of compelling children to make critical health decisions on their own and then, through the MCRs, providing the vehicle for children to obtain healthcare in secret.

“The MCRs are a critical part of [the] defendants’ propaganda machine. Without the MCRs, children cannot receive these vaccines in the absence of parental consent.”

Videos pressuring teens promote ‘name calling, outright bullying and violence’

CHD and the parents suing the city argued that whether or not their children were vaccinated without their consent, they were injured because the regulations put their children at risk of imminent vaccination, violating their constitutionally and statutorily protected parental rights.

The parents — all of whom are either residents of Philadelphia or travel frequently to Philadelphia — said they are concerned their children may be pressured into vaccination when they are in the city because of measures put in place targeting teens to get vaccinated.

During the COVID-19 pandemic, Philadelphia, like the district, created a “pressure-cooker environment,” in which children could be psychologically manipulated into defying their parents and getting vaccinated, the plaintiffs allege.

The plaintiffs’ memo included several examples illustrating the intense pressure teens could be subject to, which along with the arguments in the brief, “exposed the underbelly of city officials’ methods of persuasion and coercion by directing extreme forms of psychologically manipulative peer pressure under the guise of empowerment, equality, freedom and health,” Ray Flores, an attorney for the plaintiffs, told The Defender.

That evidence included two videos that Flores called “cringeworthy.”

In one video, teens perform a skit where one teen pressures another to go with her to get the COVID-19 vaccine, by pushing her and calling her an idiot. The video, Flores said, “promotes name calling, outright bullying and violence.”

No parents are present or referenced and the teens in the skit go to get vaccinated alone.

After the skit, another teen presents a series of “facts” about the vaccine, including a guarantee that the vaccines do not affect DNA, they have no adverse effects and that they provide immunity to the virus.

“We provide the facts, so you can get the vax!” the teens chant.

In a second video, a “Teen Vaxx Ambassador” talks about how effective “teen-to-teen” conversations are in convincing others to get vaccinated. She also details how they make getting the vaccine fun by creating a “party-like atmosphere” around the vaccine.

“The city indoctrinates these children to convince peers to make rash decisions without any professional information,” Flores said. “Given that these children can receive nearly any injection without parental permission, the dangers are clear and obvious since a plethora of vaccination sites are located within the city limits.”

The memo also included links to several news stories celebrating the city’s policy allowing minors to consent to vaccination and promoting vaccination to teens.

The plaintiffs also underscored several key arguments from the complaint.

They argued that Philadelphia’s regulations conflict with the consent requirements of the National Childhood Vaccine Injury Act of 1986 (NCVIA), the federal law that has primacy over conflicting local laws on such matters, according to the U.S. Constitution, and must be applied equally in all places.

They also argued that children are not “capable of providing informed consent” for vaccines, as the regulations suggest, because the vaccine information sheets or COVID-19 fact sheets are not written for children to understand. Additionally, children may not know their health history, or understand and be able to navigate the process for identifying and seeking compensation should they become vaccine-injured.

The memo reiterates that vaccinating a child without parental consent violates parental constitutional rights to direct their children’s upbringing. In their motion to dismiss, the defendants argued this right is only violated if the child is compelled to be vaccinated.

The plaintiffs countered that the injury occurs when parents are deprived of their right to make the decision in the first place.

They wrote:

“The Defendants have crafted a procedure to clandestinely bypass parents lawfully exercising their authority. Meanwhile, the City has ratcheted up the pressure on children whose parents have opted out of vaccines and even on children who do not know their vaccination status and thus even are susceptible to over-vaccination.

“The City has publicly and vocally encouraged children to be vaccinated as part of its program to do an end-run around parents.”


Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.

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.

January 25, 2024 Posted by | Civil Liberties, War Crimes | , | Leave a comment

NEW DATA REVEALS TSUNAMI OF COVID-19 VACCINE DEATHS

The Highwire with Del Bigtree | January 18, 2024

Systems Engineer & Analyst, John Beaudoin, Sr., delves into his recent testimony before the New Hampshire Senate where he shared the extensive data he has gathered from death certificates, revealing a concerning surge in blood and circulatory-related deaths aligning with the COVID-19 vaccine rollout. Beaudoin and Del discuss how through cross referencing of data sets, Beaudoin was able to match death certificates to VAERS reports from those who died after a COVID-19 vaccine. Hear some of the heartbreaking instances of young patients whose deaths are directly linked to the vaccine, exposing a disturbing trend of fraudulent coding on death certificates to conceal the true impact of vaccine-related fatalities.

January 21, 2024 Posted by | Timeless or most popular, Video, War Crimes | , | 1 Comment

The long awaited debate of Covid science: Experts rebut the expert opinions of BC’s College of Physicians and Surgeons

The College is trying to punish Dr. Charles Hoffe for numerous 100% scientifically accurate statements on multiple aspects of Covid science.

Pierre Kory’s Medical Musings | January 18, 2024

Canadian community doctor Dr. Charles Hoffe was one of the first to notice something was “wrong” with the vaccines in April 2021 after he witnessed terrible injuries (strokes etc.) and even a death in the patients he was vaccinating. He then wrote an open letter to the College of Physicians and Surgeons of British Columbia with his observations and concerns, suggesting that perhaps the jabs should be put on pause until their safety could be more assured. One paragraph from the letter said:

“In our small community of Lytton, BC, we have one person dead, and three people who look as though they will be permanently disabled, following their first dose of the Moderna vaccine. The age of those affected ranges from 38 to 82 years of age,” he wrote.

Hoffe was then banned from working in the local emergency ward and other provincial hospitals. He later submitted more than a dozen claims of vaccine injuries on behalf of his patients, but all were denied validity.

*For more background, click tweet below by Dr. Mark Trozzi, another persecuted Canadian doctor for a summary of what is happening to Hoffe (and includes a powerful speech by Dr. Hoffe).

Through FOIA obtained emails, Hoffe and his lawyer discovered that the College’s first and only internal response was to find someone to report Dr. Hoffe for writing the letter. There is no evidence of any concern for the patients nor a request or investigation into Hoffe’s patient records. They instead simply told him each report was a “coincidence” and that it was best if he stop talking about this issue in the hospital. Both shocking and unsurprising I know.

He instead rightly began speaking out publicly and the three mainstream media outlets in Canada (there are only 3) have in turn, viciously and repeatedly done hit jobs on him, making him appear as the least credible doctor in the country (which my readers know well is a censoring tactic, i.e. make truth tellers appear as un-credible as possible so no-one will listen to or believe them).

More recently the College began an investigation into Dr. Hoffe for numerous public comments he has made since his letter. This is a summary of the supposedly inaccurate statements made by Dr. Hoffe:

6.1. Patient Safety and Experimental Nature ………………………………………………………………… 23
6.2. Potential Harms to Fertility in Women …………………………………………………………………… 27
6.3. Myocarditis in Children ………………………………………………………………………………………. 30
6.4. Ivermectin for Treatment and Prophylaxis ……………………………………………………………… 33
6.5. Ivermectin Access ……………………………………………………………………………………………… 36
6.6. Harms to Pregnant Women …………………………………………………………………………………. 39
6.7. Microscopic Clotting ………………………………………………………………………………………….. 42
6.8. Adverse Events Following Immunization ………………………………………………………………… 46
6.9. Harms to Children ……………………………………………………………………………………………… 50
6.10. Vaccine Shedding ………………………………………………………………………………………………. 53
6.11. Statement (1). April 4, 2021, email to Dr. Carol Fenton from Dr. Charles Hoffe………………. 56
6.12. Statement (2). April 5, 2021, open letter to Dr. Bonnie Henry from Dr. Charles Hoffe ……… 60
6.13. Statement (3). April 21, 2021, email to Dr. Carol Fenton from Dr. Charles Hoffe …………….. 64

The College then hired an “expert” named Dr. Trevor Corniel who submitted a 151 page report with a whopping 191 references. In that report he argues that each and every public statement made by Dr. Hoffe on the above topics was “incorrect,” “misleading,” “inflammatory” and violated both the College “Prudence Standard” and “Harm Reduction Standard.” Know that these “standards” are ethical codes of conduct that members of the College must abide by (remember ethics?). In my expert opinion, I argue that Corneil (knowingly or unknowingly) amassed data from fraudulent peer-reviewed literature and captured public health agency recommendations to support his conclusions that Hoffe is in violation of practice standards.

If Dr. Hoffe were to be found guilty as argued by Dr. Corniel, he is at risk of losing his livelihood (license) and could be fined up to $100,000. So they want to end his career and then take his money. I wonder how many future doctors will speak up against the next Big Pharma-Government fraud in Canada once Hoffe’s fate becomes well-publicized? As far as I can tell, Canada only had less than a handful of publicly outspoken doctors and scientists in Canada during Covid (Charles Hoffe, Byram Bridle, Mark Trozzi, Paul Alexander, and William Makis – if I am leaving anyone out, I apologize). However, good luck hearing advice from un-conflicted doctors in the next pandemic.

**Since first posting this, subscribers have sent me other names of outspoken and/or persecuted Canadian docs so the list is larger than I thought: Rochagne Killian, Patrick Phillips, Chris Shoemaker, Daniel Nagase, Rodger Hodkinson, Patrick Phillips, Chris Milburn, Laura Braden, Michael Palmer, Crystal Luchkiw..

Anyway, Hoffe’s lawyer, Lee Turner of Doak Shirreff Lawyers LLP in Kelowna, B.C. engaged me to defend a number of Hoffe’s statements regarding ivermectin and shedding. I was proud to learn I was joining an All-Star team of medical dissident experts defending him such as Jessica Rose, Peter McCullough, Kevin McKernan etc. I plan to ask them to also post their expert reports on Substack, and I will create a central post linked to all for those interested.

Of note, Lee has been practicing trial law in British Columbia for 30 years and is experienced in administrative, public health, and personal injury law. He has been very busy in Covid as he has represented numerous nurses, physicians and other health care providers and individuals who were negatively impacted by Canadian Covid-19 public health measures and mandates (which as you know were far more draconian than here in the U.S).

I elected to do the case pro-bono and began by reading Corneils “expert” report which viciously and repeatedly attacked Hoffe for his many accurate statements. I was so infuriated after reading it, I said to myself “Game on (expletive)” and immediately launched into a writing and researching frenzy over the last 5 days and I would say I put over 20 hours of work into my report. It is 47 single spaced pages with who knows how many hyperlinked references.

I hope I am not being too full of myself but I want to share what Lee Turner wrote to me after he read it:

“Pierre, I don’t even know how to express how incredible the information in your report is. It is one of the most thorough and well written expert reports I have read in my 30 year career. And I have read a lot of expert reports. I made a few minor corrections to spelling, and adding in punctuation (periods, commas or colons) and that was it. I think it is very well written and contains powerful evidence.”

Lets go through Count #1 against Dr. Hoffe shall we? … continue

January 19, 2024 Posted by | Corruption, Deception, Science and Pseudo-Science | , | Leave a comment

mRNA vaccines lead to unwanted proteins – but what does it mean?

New research has experts angered by the “complete and utter regulatory failure” to ensure patient safety

BY MARYANNE DEMASI, PHD | JANUARY 16, 2024

After three years on the market and billions of doses later, the mRNA COVID-19 vaccines continue to throw up surprises.

A landmark study, published last December in Nature, has reignited concerns over the safety of the vaccines.

The study, by highly credentialled UK researchers, found that in addition to spike protein, Pfizer’s mRNA vaccine can instruct cells to produce other ‘off-target’ proteins, which are foreign to the immune system.

How does it happen?

The researchers say that ribosomes, which are responsible for decoding the mRNA in cells, can slip and misread the coded instructions about 8% of the time – known as “ribosomal frameshifting.”

They say the ‘glitch’ has to do with how the mRNA in the vaccine has been genetically modified.

Unlike naturally-occurring mRNA, the mRNA that exists in the vaccines has had a ‘uridine’ base replaced with a ‘N1-methyl pseudouridine’ (to stabilise it) and unfortunately, has made it prone to reading errors.

But are these ‘off-target’ proteins harmful?

At a press briefing, the study researchers insisted there were no safety concerns, and that their findings did not indicate the mRNA vaccines were unsafe.

The BBC characterised the glitch as a “harmless tiny slip” in mRNA gene translation.

Science said there was “nothing alarming” about the study, and interviewed experts who reiterated the absence of adverse events associated with these off-target proteins.

However, David Wiseman, a research scientist involved in medical product development, is not so convinced. He, and his co-authors, published their comments in Nature.

I spoke with Dr Wiseman about his concerns and what this research might mean for patient safety.

DEMASI: Thanks for speaking with me Dr Wiseman. How concerned are you about these latest findings?

WISEMAN: I’m very concerned. This raises more questions about the long-term safety of the mRNA vaccines.

DEMASI: Before we discuss what they found, can you explain the purpose of the study?

WISEMAN: Well, these researchers asked a simple question – are the instructions contained within the mRNA of the vaccines being faithfully carried out.  Or put another way, does the body make the spike protein it’s supposed to make, as instructed by the mRNA’s code.

It’s like saying here’s a recipe with instructions on how to make a cake – it’s grandma’s cake recipe. These researchers wanted to know if the mRNA could accurately give instructions on how to make Grandma’s cake or whether it would produce a corrupted version of grandma’s cake.

These researchers obviously knew from the literature that modifying some of the bases in the vaccine’s RNA – as was the case for the mRNA COVID-19 vaccines – that it might cause misreads of different kinds. It’s known as ‘frameshifting.’

DEMASI: And what exactly did they find?

WISEMAN: They found the Pfizer vaccine can cause your cells to make proteins that they are not supposed to make – you end up with what I call “Pfrankenstein proteins.”

DEMASI: Because sometimes there are errors in the way the mRNA is read?

WISEMAN: Yes. Imagine the following three-letter English words ABE DAN TEA TON ERA TWO – the letters are like the code on the mRNA. Now instead of starting to read the sentence at the letter “A” of the first word, you frameshift to the next letter – the letter “B.”

That means that all the other letters are shifted to the left and it will give you a new sentence with three-letter words BED ANT EAT ONE RAT etcetera.

So, the new words have a completely different meaning from the original words. This is what happened in the body of some people vaccinated with Pfizer’s product.

New unwanted “off-target” proteins were produced, that actually led to an “off-target” immune response.

DEMASI: So, were these off-target proteins detected in the blood of people who’d been vaccinated?

No, they did not measure these proteins in the blood of people who’d been vaccinated.

These researchers did something similar to what I did with the six English words – they “predicted” what some of these off-target proteins would look like, had there been a problem with frameshifting.

They made these frameshift proteins in the lab – about 30 or 40 of them – pooled them together in a test tube and then exposed them to blood lymphocytes (white blood cells that mount the immune response) taken from people who’d been vaccinated.

What they found in about 25 to 33% of people who’d received Pfizer’s product, was that their lymphocytes, responded immunologically when exposed to these frameshift proteins in a test tube.

It means their lymphocytes had seen the proteins before – their immune system had already been primed from a prior exposure, presumably after that person had received the mRNA vaccine.

DEMASI: They also tested samples from people who’d received the AstraZeneca vaccine and saw no immune reaction – can you explain why?

WISEMAN: The AstraZeneca vaccine is a different technology. It is a DNA vaccine and does not have the uridine modification that is causing the frameshifting in the mRNA vaccine.

So, it’s not surprising that the lymphocytes from people given the AstraZeneca vaccine did not react to these frameshift proteins, because they’d never seen them before.

DEMASI: They didn’t study people vaccinated with Moderna, but would you say the problem is likely to happen with Moderna’s vaccine too?

WISEMAN: Yes, I would because it’s also an mRNA vaccine and contains the same sort of uridine modification as the Pfizer vaccine.

DEMASI: OK, so making proteins you’re not supposed to make sounds bad, but the media coverage seemed to suggest there wasn’t a problem….

WISEMAN: What you have to realise is that your body is being hijacked, not just to produce spike protein, but also to produce other, what I call, “Pfrankenstein” proteins that are completely uncharacterised.

We don’t know what they are, what they do, for how long they’re made or how long they last in the body, and we have no idea what their toxicity is. From the Nature paper however, we do know that these unwanted proteins elicit immune reactions in the body.

DEMASI: What could these immune reactions lead to? You were concerned about autoimmune conditions?

WISEMAN: Yes. These researchers showed that frameshifting could create chimeric proteins.  Basically, as the ribosome reads the code for the spike protein, it may slip in the middle of reading the code. So, the first half is spike protein, and the second half is a Pfrankenstein protein.

Now, just imagine one half can still attach to the ACE2 receptor on cells but on the other end, you’ve got this Pfrankenstein protein dangling outside of the cells.  Your immune system is going to destroy the cell because it looks foreign, and now you’ve got something that looks like an autoimmune condition.

Or you could have a protein that turns out to be not necessarily identical, but sufficiently similar to another protein in our body like a hormone and it ends up mimicking the hormone’s activity and disturbing your endocrine system.

DEMASI: But the study authors said there were “no adverse events” associated with these frameshift proteins.

WISEMAN: The authors wrote, “…there is no evidence that frameshifted products in humans generated from BNT162b2 vaccination are associated with adverse outcomes.

But they only looked at 21 people who received Pfizer’s vaccine, so you cannot call that a serious safety study by any stretch of the imagination.

And how did they select these people?  The volunteers were part of another government funded study and had not reported undue effects from vaccination. Since they did not study subjects who had reported adverse vaccine effects, the selection of participants was probably biased.

DEMASI: The authors of the study said that with some tweaks they could identify potential slips and reduce reading errors…..

WISEMAN: Right, and this work should’ve been done by the vaccine manufacturers and by the regulators before the product was authorised and given to billions of people. They’ve asked people to take a vaccine, and put it into children and they have no clue what is happening inside the body.

What they’re trying to say now is that there have been no problems identified in 21 people, but in the future there may be problems, so we should just keep studying it.

Are you kidding me? What they’re saying is that ‘we will inject you first and ask safety questions later.’ It’s not good enough.

It’s just like the retired Pfizer executive admitted in a Nature article, “We flew the aeroplane while we were still building it.”

DEMASI: Shouldn’t the drug regulators be all over this?

WISEMAN: This has been a complete and utter regulatory failure. The 2021 WHO guidelines say that for mRNA vaccines the manufacturers have to disclose all the sequences and unexpected reading frames. They were required to have done this work already… The FDA should have been looking at it.

The mRNA vaccines are causing our bodies to produce uncharacterised proteins, with unknown toxicology, that produce an immune response of unknown clinical significance. The dereliction of duty by regulators shows how they’ve sunken to an all-time low.

January 17, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular, War Crimes | | 1 Comment