Mass walkouts against vaccine mandates begin NOW: November 8 - 11... but watch out for false flag operators exploiting protest crowds

Global mass walkouts have begun today in protest against unconstitutional vaccine mandates. The peaceful protest continues for four days, through Nov. 11th, and participants are asked to remain peaceful, avoid bringing weapons of any kind to such protests, and to film everything in order to document attempted false flag operations by deep state saboteurs. The world is pushing back hard against criminal governments that now seem to be engaged in acts of medical terrorism against their own citizens. With post-vaccine deaths now skyrocketing in Emergency Rooms across the USA and the world, it's becoming increasingly clear to millions of people that the vaccines are depopulation weapons being deployed against humanity. See this presentation by Dr. David Martin for more details on the medical treason being committed against humanity: (audio level is low in the original video)As I explain in my Situation Update podcast, below, this protest week presents a heightened threat window for deep state operatives to carry out false flag operations in which they would deliberately target a drug company, a vaccine clinic or a hospital in order to try to paint anti-vaxxers as "terrorists." The lying mainstream media isn't in the news business; they're in the theater business. And they need new theater to desperately change the narrative and try to halt the rising backlash against vaccine mandates. Now 29 US states have joined in suing the Biden administration over the federal vaccine mandate, and on Friday, the Fifth Circuit Appeals Court issued a stay of the order, pending further legal action. https://twitter.com/GregAbbott_TX/status/1457042568332652555 The Biden administration promises to fight for the order, a dangerous overreach of power for OSHA, which is supposed to be focused on workplace safety, not global pandemics.

Vaccine mandates are government OWNERSHIP over your body... slavery!

When someone else has control over your body and can determine what goes into it, you no longer "own" your own body. Vaccine mandates are a form of medical slavery, and they violate numerous amendments in the Bill of Rights, including the Fourteenth Amendment. Vaccine mandates are a violation of civil rights and human rights, and they place the government in the positioning of being able to order you to be injected with literally anything they want as long as they create a sufficient crisis and label the injection a "vaccine." (Note that the CDC had to change the definition of vaccines in order roll out approval for mRNA interventions...) Those who are demanding forced vaccinations are simultaneously demanding mass slavery and total obedience to a death cult regime that's now clearly engaged in acts of democide -- death by government. Ultimately, this issue is likely to end up in front of the US Supreme Court, and if the justices there have any humanity at all, they must strike down vaccine mandates as blatantly unconstitutional. If they don't, there will be calls for state-level nullification of OSHA and the entire federal government. It will be time for red states to denounce the criminal cartel in D.C. -- conspiring with Big Pharma, Big Tech and Big Media to carry out genocide against humanity -- and establish new nations that respect human rights. In effect, this country may go to war over vaccine mandates unless the Supreme Court smacks them down first. The Biden regime is trying to drive a wedge through America with the illegal vaccine mandate, and the momentum is now turning against him. That's a positive sign, but it also means the radical Marxists running the Biden regime will become increasingly desperate in their attempts to assert control and "authority" over the masses. This is why false flag operations are now at the top of their list. Brighteon.com/fca25b68-81fc-440f-bf36-d0bbcfc478b2

Regeneron Presents New Phase 3 Analyses Showing a Single Dose of REGEN-COV (casirivimab and imdevimab) Provides Long-term Protection Against COVID-19

Regeneron announced additional positive results from a Phase 3 trial which assessed use of a single dose of investigational REGEN-COV (1,200 mg administered via 4 subcutaneous injections) to prevent COVID-19 in uninfected individuals. REGEN-COV was able to reduce the risk for SARS-CoV-2 infection by 81.6% during the second to eighth month follow-up period and maintained the 81.4% risk reduction rate seen in in the first month. Initial data were published in The New England Journal of Medicine in September. 

REGEN-COV is composed of two monoclonal antibodies that block the infectivity of SARS-CoV-2 using the company’s VelociSuite and VelocImmune technologies. 

The double-blind, placebo-controlled trial enrolled people who lived in the same household as an individual who was diagnosed with SARS-CoV-2 within the prior 4 days. During the trial, participants were tested weekly for SARS-CoV-2 during the initial month (4 weeks), as part of the primary analyses. Following this, from months 2-8 (week 5 to week 32), participants were to be tested if they developed any COVID-19 symptoms.

Per the previously published data, the trial met its primary endpoint, reducing the risk of COVID-19 (i.e., laboratory-confirmed symptomatic SARS-CoV-2 infections) by 81.4% within 1 month of receiving REGEN-COV. The new results are from a pre-specified analysis for the following 7 months, throughout which an additional 45 symptomatic infections occurred. This includes results from 1,683 people who were not infected with SARS-CoV-2 and did not have antibodies for SARS-CoV-2 (seronegative) at baseline. During this time period, REGEN-COV continued to prevent infection, without requiring additional doses. In addition to the 81.6% risk reduction, data showed an 81.5% reduced risk of developing COVID-19 at any time during the 8 months after receiving REGEN-COV. In addition, during the 8-month assessment period, 0 subjects in the REGEN-COV group were hospitalized due to COVID-19, compared to 6 in the placebo group. 

The FDA has granted Emergency Use Authorization to REGN-COV for the treatment and post-exposure prophylaxis in certain high risk individuals.

In October the FDA accepted a BLA for REGN-COV for Priority Review and assigned a target action date of April 13, 2022

About the REGEN-COV Antibody Cocktail

REGEN-COV (casirivimab and imdevimab) is a cocktail of two monoclonal antibodies that was designed specifically to block infectivity of SARS-CoV-2, the virus that causes COVID-19, using Regeneron’s proprietary VelocImmune® and VelociSuite® technologies. The two potent, virus-neutralizing antibodies that form the cocktail bind non-competitively to the critical receptor binding domain of the virus’s spike protein, which diminishes the ability of mutant viruses to escape treatment and protects against spike variants that have arisen in the human population.

Proton wins appeal in Swiss court over surveillance laws

A Swiss court has upheld the appeal of Geneva-based Proton, a provider of secure and anonymous email services, limiting its obligation to monitor traffic and retain data for surveillance purposes.

This content was published on October 23, 2021 - 16:03October 23, 2021 - 16:03

Reuters/jdp

On Friday, the Swiss Federal Administrative Court upheld Proton’s appeal against the Swiss Post and Telecommunications Surveillance Service (PTSS) over obligations to store data and monitor email traffic. The court confirmed that email services can’t be considered telecommunications providers in Switzerland, and therefore are not subject to data retention requirements.

Proton founder and CEO Andy Yen said the ruling was an "important first step" in its campaign to advance privacy and freedom, reported Reuters.

"We expect there to be further attempts to force tech companies to undermine privacy in both Switzerland and abroad, and we are committed to continuing to challenge this through both our encryption technology and through the courts," he said.

PTSS had decided in September 2020 that Proton could no longer benefit from limited surveillance obligations but had to store data necessary for surveillance and be available to answer questions. The court overturned this and sent it back on appeal.

Last month ProtonMail found itself in the centre of a social media storm after it emerged that the company shared the IP address of one of its users as part of a French investigation that led to the arrest of climate activists. However, the company said that it had to comply with a Swiss court order to provide data that helped identify the activists.

From its inception, the company has prided itself on strict user privacy and security. The recording of IP addresses is only allowed in “extreme criminal cases” according to the company’s transparency report.

ProtonMail was founded in 2013 at the initiative of a group of scientists from CERN in Geneva and the Massachusetts Institute of Technology (MIT). Proton says it is the largest secure email provider and uses end-to-end encryption and state-of-the-art security features.

NFL Star Not an ‘Anti-Vaxxer’ Shuns Vaccine & Depends on Ivermectin & mAbs

Aaron Rogers, the Green Bay Packers star quarterback went on the record for all that not only is he unvaccinated but that he is taking ivermectin.  He has declared he has concerns for allergic reactions to the COVID-19 vaccines while he also stepped up his criticism of what he calls the “woke mob,” hell-bent, so he claims, on cancelling his point of view from collective existence.  TrialSite can attest that while this is a pro-vaccine and pro-pharma media platform the tracking of ivermectin studies as well as chronicling of COVID-19 vaccine studies demonstrating durability challenges has most certainly triggered unfortunate censorship of this media.

The 37-year-old football star recently tested positive for COVID-19 reported many mainstream media.  Under fire for not getting his two jabs, the reigning NFL MVP declared he commits similar dedication to studying COVID-19 vaccines as he does prepare for a game.

Recently covered by numerous media Rogers went on the record “Look, I’m not, you know, some sort of anti-vax flat earther. I am somebody who is a critical thinker” declared the star athlete on The Pat McAfee Show on Sirius XM

He continued “I believe strongly in bodily autonomy and ability to make choices for your body: Not have to acquiesce to some woke culture or crazed group of individuals who say you have to do something. Health is not a one-size-fits-all for everybody.”

Like many celebrities and people of means NFL star was able to secure a monoclonal antibody (mAbs) treatment while taking the ivermectin, like what Joe Rogan did when he was infected with SARS-CoV-2, the virus behind COVID-19.   Much of the common population struggles to find access to mAbs while the ivermectin supply in physician off-label use scenarios becomes increasingly difficult to access due to pressure on pharmacies. 

Rogers disclosed that he has become friend with the nation’s most popular podcast star declaring on the Sirius XM show “I consulted with a now good friend of mine Joe Rogan, after he got COVID, and I’ve been doing a lot of stuff that he recommended.”

Super Bias or Protecting the Public?

The mainstream media continues to emphasize that the drug is primary used to ‘deworm animals” which is only a partial truth. In fact, the drug has done wonders for the developing world to help eradicate River Blindness in Africa as part of the tremendously successful Mectizan program. Called a “wonder drug” the developers won the 2015 Noble Prize while over 60 studies indicate some positive data points. Yet most health authorities don’t concur with the quality of these studies. 

However, TrialSite attests considerable mainstream media, as well as social network bias including, and unfortunately a scandalous move by the U.S. Food and Drug Administration (FDA) to delegitimate the drug—see the article hereTrialSite secured an FOIA-based email showcasing high-level operatives in the ‘Gold Standard’ agency bragging about how many tweets their “snarky” campaign on Twitter titled ‘You’re not a horse.’ While weekly legitimate off-label prescriptions went from about 3,000 to nearly 90,000 in America, the FDA sought to stop this by conflating this latter legitimate use from the former illicit self-medication-based use.

TrialSite includes a more unbiased fact sheet on ivermectin here. This media shared that there is no certain proof that the drug helps, however we have chronicled account that there are most certainly accumulating positive data points that suggest ongoing study at proper dose regimens.

Moreover, the drug’s safety profile is well known and the federal government should not be in the business either directly or indirectly of intervening between doctors and their patients–even if it is done indirectly through physician and pharmacy societies and the mainstream media which has become highly corrupted at this point. Regardless the effort to reduce access is most certainly working.

Based on the enormous amount of taxpayer money pouring into pharmaceutical companies during the pandemic—chronicled every step along the way by this media platform—it becomes ever more apparent that industry has captured regulatory and health agencies at the federal level. This industry capture reaches globally, permeating the  World Health Organization (WHO) for example as well.  The present-day drug development and treatment paradigm driving pandemic response must be critically reviewed and evaluated for reform–at least during emergency conditions.  More than likely the winds of political change will intensify, sweeping in sweeping changes starting next year as too many common-sensed folks smell a highly biased, corrupted reality.

95% of Adults in Maine Vaccinated while Pandemic Continues to Rage: Reset Needed?

TrialSite recently shared with the community an unfolding lawsuit in Maine addressing vaccine mandates and the 661 deaths associated (but not proven) with the COVID-19 vaccines. At a Senate hearing last titled “Next Steps: The Road Ahead for the COVID-19 Response” U.S. Senator Susan Collins https://www.collins.senate.gov/ asked the nation’s top health leads such as Dr. Anthony Fauci of the National Institutes of Health as well as Dr. Rochelle Walensky, director of the Centers for Disease Control and Prevention (CDC) some pressing questions on many people’s minds. One key question for Fauci: Given that the State of Maine is one of the heaviest vaccinated places in America why have there been such a high growth in overall infections, as well as breakthrough infections?  The topic of purported vaccine associated deaths were not candidly addressed.

Representative Collins, a moderate Republican, recently shared the hearing in the form of a press release.  While Maine has the fourth highest vaccinated population proportionately the New England state now experiences the worst surge yet when factoring in total number of cases.  Even the number of deaths now approach the previous worst surge back before any vaccination was occurring.  This obviously has raised considerable concern.

Collins shared with Fauci that 95% of Mainers over age 65 have been fully vaccinated.  Nevertheless, over the past seven days, Maine has the 15th highest current Covid-19 case rate on a per capita basis and the 22nd highest death rate on a per capita basis among U.S. states.  In addition, Maine has recently experienced a six percent increase in hospitalizations, an 18 percent increase in people in the ICU, and a 37 percent increase in people on ventilators.

The Senator declared:

 “First, let me make clear that I believe in the efficacy of vaccines and have encouraged my constituents to become vaccinated,” said Senator Collins.  “But I’m hoping you can explain what appears to be a contradiction when I look at the data for the State of Maine. Maine ranks in the top five states in the [percentage] of people…who have been vaccinated.  Can you explain to me why a state that has done a terrific job in getting people vaccinated is seeing this surge in cases that is overwhelming our hospitals and causing great fear, and pain, and loss?”

 Fauci came back with what as really a non-answer:

Dr. Fauci responded that Maine’s high caseload is due to COVID-19 infecting unvaccinated populations as well as breakthrough cases among the vaccinated. 

 POTUS’ chief medical advisor continued to downplay the mounting problem attempting to position the issue as simply not achieving 100% vaccination:

 “[A] vaccinated compared to an unvaccinated person has a multifold less likelihood of being infected, a multifold less likelihood of being hospitalized or dying.  I think there were probably confounding multiple factors going into the difficult situation that your citizens in your state are going through, but there’s no doubt that the vaccines are clearly much better in the sense of protecting you from infection, hospitalizations, or death compared to the unvaccinated.”

However, TrialSite has accumulated dozens of national and regional studies now that indicate vaccine durability represents a growing problem. Meaning that the vaccines will wane in effectiveness leading to growing breakthrough infections, hospitalizations and even deaths.

CDC Director’s POV

Turning to Dr. Walensky, Senator Collins raised the promising “test-to-stay” approach that allows asymptomatic students who test negative for COVID-19 to remain in school rather than quarantining after another student or a staff member has tested positive for the virus.  A study in the peer-reviewed British medical journal The Lancet found that case rates were not significantly higher at schools that allowed close contacts of infected students or staff members to remain in class with daily testing than schools that required students to quarantine at home. Senator Collins previously pressed the Secretary of Education to consider this method in September.

“Dr. Walensky, parents, teachers, and pediatricians have all talked to me about the learning loss, the emotional and behavioral health problems, that have occurred among children due to their not being in school,” said Senator Collins.  “Brown University professor Emily Oster has expressed great frustration with the CDC being slow to take a stronger position in favor of test-to-stay… Another public health expert said simply ‘It’s madness to quarantine school children.  The CDC policies hinder learning and provide no meaningful reduction in COVID transmissions.’ My question for you is, why doesn’t the CDC issue guidance or recommendations to encourage school districts to adopt test-to-stay in order to avoid these highly disruptive quarantines of students who are asymptomatic and could be tested?”

In response, Dr. Walensky said the CDC is “working with local jurisdictions now to demonstrate the domestic data here in the United States that this practice works, it’s safe, it’s effective, [and] it gets our children back to school. And importantly, we recognize that jurisdictions are actually doing this and other jurisdictions may want to.  And in that context, we’re doing peer-to-peer matching of schools that are interested in doing the test-to-stay practice and having them talk to schools that are also doing it so they can use the implementation strategies that a school has already used.  So we’re actively studying this so that we can provide the data on it working, and we’re actively encouraging it as a promising practice.”

Conclusion

Public health authorities and the current political leadership continue to take the rigid stance that universal vaccination represents the only key next step to overcome the pandemic. However mounting data indicates that vaccination just cannot stop such a malleable pathogen by itself.  This is not a disease that can be eradicated via vaccination. Moreover growing reports of vaccine-related safety-related issues must be taken seriously and not continually censored in an attempt to systematically discount the data.

TrialSite suggests that unfortunately the pandemic has become too politicized and forces form multiple points of view will attempt to exploit that fact to advance political, economic and social agendas.

The growing evidence of vaccine-related adverse events must be accounted for—simply ignoring them will lead to possibly extreme political reactions.

What is needed is a step back, objective review of the true situation and collaborative, bipartisan efforts (in America) to adjust and extend approaches that further protection from the disease while ensuring civil liberties and mission critical economic considerations are factored into any agenda moving forward.

Call to Action: You can review the Senate hearing here.

Philippines FDA Grants Compassionate Use for Molnupiravir while Merck to Charge 11X for the Drug in America vs. Southeast Asian Nation

Merck now positions molnupiravir as a “great equalizer” offering antiviral treatment to help low-and-middle-income countries (LMICs) assistance to manage the pandemic as it transitions to endemic conditions.  The Philippines government has purchased 300,000 courses and the nation’s Food and Drug Administration has authorized “compassionate use” of the drug for 31 hospitals reported agency Chief Rolando Enrique Domingo recently.  While the United States has been the epicenter of the pandemic, with more SARS-CoV-2-related deaths than any other nation Americans will pay top dollar for Molnupiravir—even though $356 million of taxpayer money went into the drug’s research and development while the U.S. government under the Biden Administration contractually committed to a purchase of $1.2 billion. Americans will subsidize the drug—and Merck profits—while in the Philippines reports are that the average health consumer there will pay between $1.97 to $2.96 per pill with a patient requiring 30 pills over the five-day course for a complete treatment regimen.  That means that while in the United States the consumer infected with COVID-19 will pay $700 or more while in the Philippines that total course will cost between $59.1 to $88.8. Even in pandemic conditions Merck will exploit the situation—charging the American consumer 11X the price as other parts of the world even through the consumer’s tax dollars helped develop the product.

With over 109 million people, the Philippines is the 13th most populated nations worldwide. This Southeast Asian nation experience a scary surge in Delta variant-based COVID-19 cases during August and September, but cases have plummeted now most recently equaling 2,389 per day based on the seven-day average. For some perspective on September 15 that seven-day average new case figure was 21,287. Deaths have been hovering at an all-time high since the summer with a total death count of 44,430. This compares to a total of 775,176 in America. 

America: Far Higher COVID Infection Rate

For comparison the death to total case ratio in the Philippines equals .015% while in the USA the death rate to cases equals 0.16%. On a per-capita basis America experiences worse infection rates at 14% while that figure in the Philippine’s equals 2.5%.  Far more people succumbed to infection in America unless this Southeast Asian nation is grossly undercounting their cases—which is possible.

Potential Ivermectin Competition Delayed

In the meantime, the big push for Ivermectin in the Philippines was continuously delayed as TrialSite has reported. As chronicled by TrialSite, the big ivermectin study called for by President Rodrigo Duterte has been in continuous delay. Not implying any conspiratorial forces, the market’s been conveniently cleared for Molnupiravir sales. Of course Pfizer’s recent positive antiviral news also offers prospective competition to Merck. But prices will be higher than what would have been the cost for ivermectin.

Call to Action:  More people worldwide need to understand how drugs are developed, approved and marketed around the world. TrialSite News can help shine some light on the subject.

Are the Scientific Journals Censoring the Science? Part 1: The Removal of the Report on Myocarditis Adverse Events in VAERS, by Elsevier and Current Problems in Cardiology Sonia Elijah

This is Part 1 of my investigative series looking into how certain experts in science and medicine, who have not gone along with the ‘official Covid narrative,’ have experienced their reports being abruptly removed from publication or have been rejected from the start.

Dr Peter McCullough, MD, MPH, one of the most cited physicians in the world, an eminent practitioner of internal medicine, a cardiologist and epidemiologist, co-wrote a report with Dr Jessica Rose, Ph.D., virologist and epidemiologist in Canada, called ‘A Report on Myocarditis Adverse Events in the U.S. Vaccine Adverse Events Reporting System (VAERS) in Association with COVID-19 Injectable Biological Products.’

The report relied solely on the data supplied by the US VAERS (Vaccine Adverse Event Reporting System), which was created by the US Food and Drug Administration and Center of Disease Control in 1990, to receive reports about adverse events (AEs) that may be associated with vaccines.

McCullough, along with Rose, examined the cardiac adverse events, mainly looking at myocarditis (inflammation of the heart muscle) following injections of the first or second dose of the three Covid vaccines- Pfizer, Moderna, and Johnson & Johnson’s Janssen. Not only was their analysis of the VAERS’s data highly alarming, but the response they received from the scientific publishers, was equally disturbing.

Their report passed peer-review and was fully welcomed and accepted for publication by Dr Hector O. Ventura, editor-in-chief of the journal, Current Problems in Cardiology, on September 22, 2021. It was published online, ahead of print, on October 1, 2021, and on Elsevier- the world’s largest medical publisher.

However, on October 15, it was ‘temporarily removed’ from both Elsevier and the online version of the periodical, without prior notice given to the authors. A week later, Diana Goetz, associate publisher at Elsevier, informed the authors that the paper was to be permanently removed from the site. This news came only five days before the pivotal FDA meeting, to review whether to give approval for the Pfizer vaccine to 5–11-year-olds.  

The main findings of the Myocarditis report:

  • Hundreds of thousands of individuals have reported adverse events (AEs) using VAERS, the primary focus of this analysis being the serious adverse event (SAE) of myocarditis.

  • Myocarditis rates significantly higher in male youths between the ages of 13-23.

  • 19 times the expected number of myocarditis cases in the vaccination volunteers over background myocarditis rates for this age group.

  • A fivefold increase in myocarditis rate was observed after dose 2 as opposed to dose 1 in 15-year-old males.

  • A total of 67% of all myocarditis cases occurred with the Pfizer BNT162b2 vaccine.

  • Cardiac injuries associated with Covid-19 are different from the clinical picture of vaccine-induced ‘myocarditis’, which has been loosely defined as a mild troponin elevation common to ICU patients of all types.

  • Vaccine-induced myocarditis qualifies as a serious adverse event (SAE) and is often associated with hospitalization in ~90% of cases.

The report highlighted: ‘It is vital to recall that children have a negligible risk for COVID-19 respiratory illness, and yet they are a high-risk group for myocarditis with vaccination.’

*2021: up to and including July 9, 2021

The surge in myocarditis cases in the US in 2021 (post vaccine rollout) can evidently be seen in comparison to previous years. Also, it’s clear looking at the graph below that younger age groups are much more affected by cardiac adverse events, primarily myocarditis.

Dr McCullough spoke to me with regards to the alarming findings of their report and in his opinion of Elsevier’s “cowardly acts of censorship.” He went on to say that “myocarditis is serious- I’m telling you as a cardiologist..There is clear cut evidence of heart inflammation being far greater than what we’d see with hospitalized Covid-19.”

McCullough cited the Tracy Høeg et al study, where a “child is more likely to be hospitalized from myocarditis from the vaccine than from Covid-19.” And “after second shot there’s been a recorded explosive increase in myocarditis.”

The study stated, ‘For boys 12-15 without medical comorbidities receiving their second mRNA vaccination dose, the rate of CAE is 3.7 to 6.1 times higher than their 120-day COVID-19 hospitalization.’

Based on the VAERS data below, strikingly, it’s young males who have been experiencing myocarditis, much more than any other age group and gender. I asked Dr McCullough the reason for this, his response was “there must be an interaction between the spike protein and human androgens or male hormones.”

In my October 26th interview with Dr McCullough, he explained that “this week is the FDA review for the Pfizer vaccine in children aged 5-11, so there couldn’t be a more important time to have a peer-review available for the world as well as for US leaders in Covid-19 to review.”

“We were shocked and appalled that Current Problems in Cardiology and its publisher, Elsevier took the paper down from the publication site..papers can only be withdrawn according to rules and the publication contract. They can only be pulled down if they’re scientifically invalid or have incorrect information-none of these criteria existed in this paper.”

He went on to offer the reason given by Elsevier for the removal of the report, “they didn’t think the paper was fully invited by the editor.” McCullough went on to make the serious claim, “Elsevier is illegally attempting to censor this paper- right at the moment when it’s needed the most, when the vaccine manufacturer is going to the US FDA and seeking approval for emergency authorisation use for children aged 5-11.”

It’s worth noting, Elsevier’s article removal policy, copied from their website.

Article removal: legal limitations

In an extremely limited number of cases, it may be necessary to remove an article from the online database. This will only occur where the article is clearly defamatory, or infringes others’ legal rights, or where the article is, or we have good reason to expect it will be, the subject of a court order, or where the article, if acted upon, might pose a serious health risk. In these circumstances, while the metadata (Title and Authors) will be retained, the text will be replaced with a screen indicating the article has been removed for legal reasons.’

It’s very hard to see how McCullough and Rose’s report met the criteria stated above, resulting in the abrupt removal of their report by Elsevier.

I sent a list of questions to Diana Goetz, associate publisher from Elsevier, about the removal of the report but she did not reply.

McCullough explained, “I still have not had anyone confront me or challenge me on these findings, or even an email exchange. The only thing that’s happened is events like this one with Elsevier, where they are, in a sense, cowardly and shameful acts of censorship- where the individual is attempting to censor out of fear…or attempting defamation- you can tell this not anywhere close to a collegial science interchange.”

When I asked him what his next steps going forward would be with Elsevier, he responded, “they will be named in a lawsuit- and there will be tremendous consequences. I can’t imagine the amount of negative press that Elsevier will receive with this overt act of censorship that’s timed perfectly to try and influence a decision regarding vaccination in children particular when the data indicates that children will be harmed more by the vaccine than helped.”

Vaccine failures

Dr McCullough went on to talk about the failures of the vaccines in preventing the transmission of Covid-19 and in making things “much worse.” He cited an observational study by Chau et al “where the vaccinated can spread and pass the virus to one another- which showed that the vaccines are nearly completely useless.” He cited a study done in China showing the estimated viral loads were x1000 times higher with the Delta variant than with prior variants in the unvaccinated era (before the vaccine rollout).

Myocarditis is a SAE (Serious Adverse Event)

Dr McCullough informed me that he told America on national TV, back in June, when the CDC and FDA had recorded 200 cases of myocarditis that it was neither rare nor mild. Myocarditis is a SAE (Serious Adverse Event) because “it can lead to either hospitalization, death, disability, or what could have caused death.” As of October 15, the case figure has jumped to a shocking 10,304 individuals. He stated, “I think it’s disingenuous that our public health officials from the CDC and the FDA have categorized this syndrome as both rare and mild.”

“The Trusted News Initiative was a railroading of the world into mass vaccination.”

When I asked what he thought about the apparent war on information going on right now- given the current climate of censorship, McCullough’s response was “it’s very clear there are vaccine stakeholders. There are entities that have staked everything in the pandemic response on the vaccines and this includes world governments and departments of public health- a large powerful consortium of vaccine manufactures and entities relating to them, the bankers, the stockholders, major media. In fact, this was announced with the Trusted News Initiative, which basically stated that this consortium was so powerful that it was going to overtly censor any information that would lead to vaccine hesitancy, no matter how unsafe the vaccines were- that meant squashing any information on vaccine safety and any information on treatment of Covid-19, so individuals could not understand that there was a treatment option.”

McCullough made it clear that in his opinion, censorship of the science by Elsevier and Current Problems in Cardiology is what he had experienced first-hand.

Alarmingly, on the same day of the interview, on October 26th, the FDA panel voted to formally recommend that children aged 5-11 be authorized to receive Pfizer-BioNTech Covid-19 vaccine under emergency use authorization. At the meeting, Dr Eric Rubin of Harvard University admitted “We’re never going to learn how safe the vaccine is unless we start giving it, and that’s just the way it goes.”