Portrait of a Corrupt Pandemic: Panel Lambasts U.S. Failures of Covid Care

Sen. Ron Johnson's "Roundtable on Covid-19: A Second Opinion" reports massive corruption to suppress doctors and early treatments and sell leaky vaccines, at a cost of hundreds of thousands of lives.

Mary Beth Pfeiffer

Jan 25

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This article is part of a publishing collaboration between RESCUE and Trial Site News. The outstanding reporting by Mary Beth Pfeiffer will be simultaneously published in both outlets. Please subscribe to Rescue and Trial Site News for incisive pandemic reporting.

Sen. Ron Johnson (center) with Drs. Ryan Cole, Peter McCullough, Pierre Kory, and Robert Malone (left to right) at his Covid-19: A Second Opinion roundtable yesterday in Washington, D.C. (Photo by Teresa Banik Capuzzo)

Corruption and malfeasance by public health agencies charged with controlling covid has allowed adoption of an ineffective, poorly tested vaccine; kept treatments beyond reach of skilled doctors and their desperately ill patients; and, moreover, led to thousands upon thousands of needless deaths.

Those were just some of the explosive revelations discussed yesterday by a panel of national experts on the monumental missteps made by the United States government’s response to the covid-19 pandemic.

The event, in a room ringed by soaring marble columns at the Russell Senate Building, was organized by U.S. Senator Ron Johnson of Wisconsin, Congress’s leading critic of the government’s failure to treat covid outside of hospitals.

Indeed, Johnson, a Republican, is potentially the only U.S. legislator to question America’s response to an issue with immense consequences for the nation’s health and future. He billed the event as a “long-overdue second opinion.”

“Two years into the pandemic, the compassionless guidelines from the NIH—if you test positive—is to essentially do nothing,” Johnson said. “Go home. Isolate yourself in fear. And pray you don’t require hospitalization.”

Amid ever-shifting government advisories—on lockdowns, masks, treatments and vaccines—what quickly became clear was that dissent would not be tolerated, Johnson and many speakers said.

“As the goalposts were moving, different viewpoints were being crushed,” he said. “The Internet was used to censor discussion and vilify anyone with a different opinion.”

The speakers, assembled in a horseshoe of tables with Johnson at the head, were asked, as were attendees, if any had been censored or limited by the government’s firmly controlled covid narrative. About four-fifths raised their hands.

The five-hour hearing painted a harsh portrait of government disregard for scientific and regulatory norms. Here are some of the themes—too many to cover in one article—from what many called a ground-breaking gathering.

Vaxxed vs. Unvaxxed

Covid vaccines have failed to prevent infection and transmission of illness, while possibly—but not certainly—avoiding serious illness, speakers said. The inoculations’ failures were cast against the vaxxed-versus-unvaxxed debate that has poisoned patient care and divided the nation.

Further, data is emerging to show that the vaccinated are as likely, or more, to infection with a new variant that is far different from the one for which it was created. Additionally, hospitalization and mortality are higher in people who are vaccinated and boosted, speakers said.

Most significantly, the vaccines have been used indiscriminately and without assurance of safety, especially for children, pregnant women and those with compromised immunity. There is vast and growing evidence that they are harming many people, speakers said. Dr. Robert Malone, inventor of the mRNA technology on which the vaccines are based, called the government’s review “grossly inadequate.”

Evidence abounds that the vaccines have led to myocarditis in young men and can alter women’s menstrual cycles, suggesting, Malone said, potential reproductive issues. For children, said Dr. Peter McCullough, a cardiologist, “the risk of the vaccines are far greater than the risk of covid. “Under no circumstances, any under circumstance, should a youngster ever receive any of these vaccines.”

Pharma Rules

Clearly, the government’s emphasis on vaccines came at the expense of treatments, including ivermectin, hydroxychloroquine, fluvoxamine and budesonide, that could have kept people out of hospitals, speakers said.

Pierre Kory, a pulmonologist and treatment advocate, had one word for this policy decision, which he repeated several times: Corruption.

“United States health agency structures and policies created over the last 50 years have tightly intertwined the pharmaceutical industry with public health institutions,” he said. The result: “relentless and repeated policies by those agencies that led to the repeated placing of pharmaceutical industry interests ahead of the welfare of U.S citizens.”  

Symbolic of a government beholden to pharmaceutical interests are the drugs approved so far. They are high priced patented pharma darlings, while inexpensive generics have been soundly rejected, Sen. Johnson noted. 

“This is a mass casualty event, and we cannot wait for randomized controlled trials that are not forthcoming,” Dr. McCullough said.

Early treatment doctors recounted, one after another, their care of thousands of patients, very few of whom were hospitalized or died.

Yale epidemiologist Harvey Risch called hydroxychloroquine a game changer that was cast aside—eagerly by the National Institutes of Health—by virtue of studies that used the drug too late in the infection. Risch said ten properly conducted early treatment trials show the drug reduced hospitalizations by 50 percent and mortality by 75 percent.

“The media has not reported any of these studies,” he told the panel. “What I see here is essentially scientific proof.” 

“I’ve kept 2,000 people out of the hospital,” said Dr. Mary Bowden, a Houston ear, nose, and throat specialist who stepped into a huge treatment void. Typical of the problem at large, one sick patient told her: “My PCP won’t see me.”

Despite her success, including on people who were obese or had diabetes, Bowden lost her privileges at Methodist Hospital for espousing ivermectin.

Hospitals Diminished

The rigid enforcement of rigid treatment protocols in hospitals has come at the expense not only of patient health but of a long-cherished culture of sound, respectful patient attention. Speakers described hospitals as wastelands of care for the covid-infected, who are separated from their families, given drugs that are at turns minimally effective, including too low doses of dexamethasone, and harmful, like remdesivir.

Dr. Paul Marik lost his thirty-five-year job as an ICU physician because he refused to comply with hospital protocols—although his own protocols had saved many of his patients’ lives. Ironically, the hospital forbade ivermectin, which has among the safest profile of any drug, but allowed remdesivir, a drug rejected from an Ebola trial, in which its toxicity caused mortality rates to soar.

 In the U.S, “850,000 poor souls have died,” Marik said. “These have been unnecessary, needless deaths.” Marik helped found Front Line COVID-19 Critical Care Alliance, which is devoted to educating and promoting early treatment—an uphill struggle.

As it stands, pharmacists are routinely refusing to fill early treatment prescriptions like ivermectin, having been scared away by media coverage and government warnings. “It’s an absurdity, and obscenity and it has to stop,” Kory said.

Sen. Johnson also held hearings on early treatment of covid in May and December of 2020, featuring early treatment physicians. His latest efforts were lauded by speakers.

To see the five-hour event, click here.

Mary Beth Pfeiffer’s reporting and most recent book, LYME: The First Epidemic of Climate Change, led her to covid-19. Both diseases have been denied and mismanaged in a corrupt health care system. LYME was just released in paperback.

The NIH is funding a new animal experiment center in Texas to develop vaccines for EBOLA… when will the next “lab leak” go down?

(Natural News) The National Institutes of Health (NIH) are YET to be held accountable for circumventing a federal moratorium on gain-of-function virology research. With the help of Francis Collins and Anthony Fauci, this risky bioweapon research was seditiously off-shored through EcoHealth Alliance’s Peter Daszak who collaborated with CCP scientists at the Wuhan Institute of Virology in China.

Not surprisingly, the first cases of SARS-CoV-2 appeared in Wuhan, China, where lethal, coronavirus bioweapons research had been conducted for years with the help of NIH grants. The goal of this research was to develop highly profitable diagnostics and vaccine technologies to preempt a future “pathogen of pandemic potential.” Not coincidentally, a genetic sequence for a coronavirus spike protein was already prepared for mRNA vaccine deployment BEFORE the World Health Organization declared a “worldwide pandemic.”

Now the NIH is funding a new animal experiment center in Texas to develop a vaccine for Ebola and other viruses. Will the quest for a lucrative Ebola vaccine also lead to the sudden appearance of a contagious Ebola strain in the years to come?

Will Texas be ground zero for future Ebola pandemic ?

The unaccountable NIH will be endorsing new research efforts in Texas to develop highly profitable diagnostics and vaccines for future Ebola strains. The Texas Biomedical Research Institute (Texas Biomed) and the Southwest National Primate Research Center are being supported by the National Institutes of Health, Office of Research Infrastructure Programs via grant number P51 OD011133. The project is also supported by a $4 million grant from the U.S. Economic Development Administration.

“Nonhuman primates are the unsung heroes of biomedical research and are essential to helping us eradicate infectious diseases here in San Antonio and around the world,” says Larry Schlesinger, MD, President and CEO of Texas Biomed. “This complex will enable us to strategically grow our colony and help ensure the nation is better prepared for future pandemics.”

The animal experiment center will be completed in 2023. Once completed, it will span 200 acres and include four new buildings that can house up to 800 primates. The primates will be used for research purposes to study infectious diseases, which includes viruses that cause hemorrhagic fever (e.g., Ebola). The center will be used to develop new diagnostic panels for a variety of viruses, including but not limited to: tuberculosis, HIV, covid-19 and Ebola. Of course, these dysfunctional diagnostic tests will eventually be used to deprive people of their civil liberties, as witnessed during covid-19 lockdowns and quarantines. No doubt, these tests will be deployed against future “pandemics” that advertise pre-selected virus strains to exploit the population. No doubt, these tests will be used to convince healthy people they are sick with a certain type of virus and will need to be force tested wherever they travel.

The animal experiment center will also develop new vaccines to preempt future outbreaks. It is being funded under the same premises that preceded the covid-19 scandal and the ensuing push for mandatory, taxpayer-funded vaccines. The risk of virus escape will be high in Texas, because pharmaceutical companies have already created a blueprint to capitalize on preemptive biomedical research. It won’t matter whether the release of future Ebola strains is intentional, unintentional or can be traced at all; the pharmaceutical racketeering that has been witnessed during the covid-19 lockdowns is a calculated blueprint that works — a well-funded juggernaut of subjugation, terror and mass human exploitation.

This is how pharmaceutical companies invest in the future:

  • They fund and erect laboratories that weaponize pathogens.

  • They prepare “vaccines” based off of these bioweapons.

  • They prepare fraudulent diagnostics that enslave the population to terror campaigns and medical tyranny.

  • They incentivize the use of harmful drugs (Remdesivir) and ventilators that don’t work.

  • They suppress information and block treatments and therapies that work.

  • They unleash their experimental vaccines which only weaken human immunity, disable, cause pharmaceutical dependence and depopulate.

  • They infiltrate government agencies to unlawfully force these products on people.

  • The severe disease and death is then blamed on a new variant, a virus of natural origin, or on people who didn’t take the vaccines.

  • They make a new pathogen (and a corresponding vaccine) and start the process over again, exploiting animals and humans again.

How many animals and humans must die to develop vaccines?

Despite all of these risks, the director of the new center is most concerned about their reputation in regards to animal cruelty. He reassured the public that the center will be all about the welfare of the animals, even though the animals will eventually be infected with potentially lethal viruses. “First and foremost, this project is about providing the best possible care for our animals,” says Deepak Kaushal, PhD, Director of the SNPRC. “Our talented and compassionate team provides exceptional care to our 2,500 primates, and these new facilities will ensure they can continue to do that well into the future.”

The center includes a state-of-the-art veterinary clinic, a central meeting space for animal care staff, and a bunch of pathology labs, where researchers will exploit the animals for infectious disease research. Animals were maimed during the development of vaccines for SARS-CoV-1, MERS and dengue virus. In a 2012 study, ferrets developed lung disease and died after vaccination and subsequent infection. In a 2005 study, mice and civets suffered from enhanced disease and become more susceptible to coronaviruses AFTER they were vaccinated. Under Operation Warp Speed, animals were spared certain suffering because the U.S. government skipped the animal trials and went straight to human clinical trials.

How many animals will die at this facility to create new vaccines, and how many future lab leaks, whether intentional or unintentional, will eventually put immune-compromised, over-vaccinated humans at risk?

Sources include:

EbolaOutbreakMap.com

Phe.gov [PDF]

TXBiomed.org

NCBI.NLM.NIH.gov

PNAS.org

Criminal complaint filed in Texas accuses COVID-19 vaccine makers and pushers of “murder” and “crimes against humanity”

A massive criminal complaint filed last week with Texas Attorney General Ken Paxton’s office accuses the makers of COVID-19 vaccines, as well as all corporate and government officials involved in pushing and distributing them, with “murder” and “crimes against humanity.”

The complaint, which was filed by Harris County resident Jack E. Boteler, represents “all interested parties and subscribed citizens and residents of the United States of America who received any Emergency Use Authorization investigational injection of genetic biologic material (mRNA or adenoviral DNA) coding for the Wuhan spike protein known to be the pathogenic structure of SARS-CoV-2 designed to provoke the human body to produce antibodies for Covid 19, commonly referred to as the ‘Covid 19 vaccines.'”

Some of those specifically named in the complaint include:

— Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases and the Chief Medical Advisor to President Joe Biden;

— George Soros, billionaire financier and globalist counter-revolutionary

— Dr. Deborah Birx, White House Coronavirus Response Coordinator under President Donald Trump

— Director-General Tedros Adhanom Ghebreyesus of the World Health Organization

— Dr. Francis Collins, former director of the National Institutes of Health

— CNN founder and billionaire media mogul Ted Turner

— Billionaire Microsoft founder and noted vaccine pusher Bill Gates

— The directors and principals of the Food and Drug Administration, Dept. of Health and Human Services; the NIH, NIAID, and several other U.S. government agencies;

— Big Pharma

— Anyone else associated with manufacturing, marketing, and distributing COVID vaccines.

“This Complaint alleges murder and crimes against humanity arising from a collection of facts, observations, expert opinions, media reports and eye-witness testimony,” Boteler’s complaint continues.

“It will show that Defendants planned and executed, jointly and/or severely, the development and release of a bio warfare toxin, referred to herein as either “SARS-CoV-2” or “Covid 19” and/or as the ‘Spike Protein’ component with the dual objectives of: 1) global depopulation, and 2) population control leading to a one-world government by inducing panic, economic hardship, terror, death and injury to global populations,” it adds.

Boteler also explained:

By employing psychological warfare mechanisms, including but not limited to media reports, public policy, coercion, deceit, mandates, bribes, travel restrictions, employment restrictions, free speech restrictions and liberty restrictions, this complaint will also show that Defendants seek to induce the global population into receiving a pre-planned experimental gene therapy commonly referred to as “Covid 19 Vaccines” in furtherance of their aforementioned objectives.

The complaint then laid out cases against Fauci, Gates and others who are listed as defendants, citing reams of data, several reports and a timeline of events spanning decades and leading up to what the complaint alleges was the purposeful release of SARS-CoV-2 after it was manufactured in a Wuhan, China lab. It also cites Fauci for allegedly funding “gain of function research” that creates hyper-infectious viruses, ostensibly for the purpose of research.

It also quotes Fauci, who reportedly met with then-President-elect Donald Trump to warn: “There is no question that there will be a challenge to the coming administration in the arena of infectious diseases. … The thing we’re extraordinarily confident about is that we are going to see this in the next few years.”

The complaint concludes, “The overwhelming sum of information presented herein, much of it incontrovertible, offers more than sufficient probable cause to believe that one or more of the named Defendants has committed the offenses alleged in this Criminal Complaint, specifically mass murder through the commission of crimes against humanity.”

Defendants “planned, coordinated, colluded and collaborated among two or more named and unnamed Defendants to design a criminal enterprise” surrounding the creation of COVID-19, says the complaint, adding they also conspired to create a biological weapon which was eventually unleashed on the world.

Sources include:

DailyExpose.uk

NaturalNews.com

Piece by piece, the official covid narrative is rapidly disintegrating

As the narrative surrounding the Wuhan coronavirus (Covid-19) global psy-op (psychological operation) continues to break down, here are five things you need to know (as explained by Steve Kirsch):

1) Even the World Health Organization (WHO) is warning against covid “booster” shots

It made sense to some people to just go along with it when it was just one or two doses. But now that governments want people to take a third or even a fourth injection for the Fauci Flu, many are saying enough is enough.

Both EEU regulators and officials at WHO now admit that booster shots do not make sense, which is why they are advising the public against taking them. There is no evidence to support a booster shot program and everybody knows it.

2) More jabs means more infections

They have been trying to hide this fact from the public, but the data clearly shows that the more shots people get, the more likely they are to develop symptoms associated with “covid.”

The unvaccinated, meanwhile, are healthier, on average, compared to their “fully vaccinated” counterparts.

3) Covid jabs are NOT safe

On top of not working as claimed, covid injections are also unsafe. Many formerly pro-vaccine doctors and other health experts are speaking out against the shots, warning that they do not work.

“This is great news,” Kirsch writes. “Nobody is going public yet, but they are all [upset] and realize they have been misled. It will not be pretty. This is of course great news.”

4) Face masks do not protect against disease (hint: they spread MORE of it)

It took a long time to get to this point, but the U.S. Centers for Disease Control and Prevention (CDC) has finally admitted that cloth masks are useless at preventing the spread of covid or any other disease.

Corrupt CDC head Rochelle Walensky had no way out of fessing up to this truth after data was published showing that face veils are more of a religious rite than a viable medical intervention.

“The other mask types don’t work either, but it will take them longer to figure out the obvious,” Kirsh says.

“P100 respirators do work but only a small percentage of people know that. I can’t wait to see Rochelle Walensky wear a P100 respirator; after all, she should be modelling best practices.”

5) Young people especially should not be getting “boosted”

Even though Tony Fauci claims otherwise, there is zero evidence to suggest that covid injections are safe or effective for young people.

In fact, many doctors and other health experts are warning against parents getting their children “boosted,” despite the fact that leftist colleges and universities all across the country are demanding them of students who wish to return to campus.

“Someone is very wrong here and for once it isn’t the WHO,” Kirsh says.

A few other things Kirsch says people should know is that remdesivir is dangerous and ineffective. It has become standard procedure to administer this drug to covid patients at hospitals across America, but only because Fauci makes money every time remdesivir is injected into a patient’s body.

Also, social distancing is a farce. MIT came out with a study back in April which found that avoiding other people and treating them like the walking plague does nothing to stop the spread of disease.

“6 feet or 60 feet made no difference,” Kirsch writes. “People still haven’t figured this out.”

One of Kirsch’s subscribers pointed out that it was obvious from the beginning that all of this was nonsense. But better late than never, right?

The latest news about the Fauci Flu can be found at Pandemic.news.

Sources for this article include:

SteveKirsch.substack.com

NaturalNews.com

DailyExpose.uk

WebMD.com

WebMD.com

CNBC.com

Comparing Breakthrough Infection Infections, Hospitalization & Death During Delta: A Real-World View

Recently a group of medical researchers affiliated with Case Western Reserve University School of Medicine, the Center for Clinical Informatics Research and Education, MetroHealth System and the National Institute on Drug Abuse, National Institutes of Health in Bethesda Maryland produced an interesting study showcased in a January 20, Research Letter in the medical journal JAMA.  Tapping into TriNetX, a federated analytics platform that accesses and makes available real world data from 63 academic medical centers representing 89 million patient records in corresponding electronic health records, the study team conducted  population-wide retrospective observational patient-level analyses exempt from Institutional Review Board requirements under the auspices of Case Western Reserve University.  The study team probed breakthrough SARS-CoV-2 infections occurring between July and November 2021 during the dangerous Delta surge of the COVID-19 pandemic.  They applied propensity score matching (factoring in demographics, social determinants of health, transplants and comorbidities known to impact risk and outcomes) for monthly incidence rates of breakthrough infections to those individuals who received the Moderna (mRNA-1273) and Pfizer-BioNTech (BNT162b2) COVID-19 vaccines.  Applying Kaplan-Meier survival and Cox proportional hazard analyses to patients for 14 days post the index event—that is full vaccination (again accessed in underlying electronic health records thanks to the federated ability of TriNetX)—they applied Hazard ratios (HRs) and 95% confidence intervals calculations based on underlying comparisons of time-to-event rates associated with the two vaccinated cohorts. So, using the TriNetX platform statistical engine with a 2-sided P < .05,the authors applied the propensity score-matched cohorts and COVID-19 vaccines, the study authors compared hospitalization and mortality in infected patients from two months post the onset of the infection. What did they find?

The authors were able to generate statistics on the following:

Moderna (mRNA-1273)Pfizer-BioNTech (BNT162b2)# Subjects62,628574,538Age CommentsSignificantly older & more comorbidities but matching harmonizes Case per 1,000 person days1.62.8

However once applying the matching the differences were mitigated.  The authors found that with the surge of Delta variant-based infections came a surge in overall breakthrough infections, noting that those incidences were greater in the Pfizer-BioNtech vaccine than Moderna’s subjects.  This figure reached 2.8 and 1.6 cases per 1000 person days by November

Note that when the authors applied the matching, they found aht the hazard rate associated with breakthrough infection was significantly higher in the Pfizer-BioNTech COVID-19vaccine –or put another way mRNA-1273 was associated with a far lower hazard for breakthrough infection then BNT162b2 (n=62584) (HR, 0.85; 95% CI 0.80-0.89).

What were some other findings?

CategoryModerna (mRNA-1273)Pfizer-BioNTech (BNT162b2)# Subjects62,628574,53860-day hospitalization risk12.7% (392/3078)13.3% (2489/18737)60-day mortality1.14% (35/3078)1.10 (207/18737)

What about the risk of hospitalization?

The authors report that when comparing the matched cohorts mRNA-1273 recipients (n -3054) experienced a lower risk of 60 day hospitalization when compared to the Pfizer vaccine (n=3054)(HR, 0.80; 95% CI, 0.70-0.91). Meanwhile they found no statistical difference for mortality (HR, 0.79; 95% CI, 0.50-1.23).

Limitations

As with all observational studies, limitations can influence the final results. For this particular study the authors include the following to consider:

  • Based on underlying patient records, this was an observational, retrospective study which introduces known limitations

  • The authors are clear that the “generalizability of the results from the TriNetX platform is unknown

  • Confounding factors could be present

  • Less than perfect matching resulted from propensity score matching

Need for Transparency

Some critiques are raised with results such as these.  While a snapshot of the data is made available in associated tables, the authors don’t explain how the results granularly trace to the data sources. The fact that there is no “generalizability” to the TriNetX platform output represents an example.   Noteworthy the JAMA editors precluded any comments—why would this be the case?

Funding

  • National Institute on Alcohol Abuse and Alcoholism

  • The National Institute on Aging

  • The National Institute on Drug Abuse

  • The National Cancer Institute

  • Clinical and Translational Science Collaborative of Cleveland

What is TriNetX

Covered by TrialSite, TriNetX is a global network of healthcare organizations and life sciences companies driving real-world research to accelerate the development of new therapies. Through its self-service, HIPAA, GDPR, and LGPD-compliant platform of federated EHR, datasets, and consulting partnerships, TriNetX markets its offering as placing the power of real-world data into the hands of its worldwide community to improve protocol design, streamline trial operations, and enrich real-world evidence generation.

Lead Research/Investigator

  • Lindsey Wang, Case Western Reserve University School of Medicine, 1Center for Artificial Intelligence in Drug Discovery

  • Pamela B. Davis, PhD, MD, Case Western Reserve University School of Medicine, Center for Community Health Integration

  • David C. Kaelber, MD, PhD, MPH, MetroHealth System, Center for Clinical Informatics Research and Education

  • Noral D. Volkow, MD, National Institute on Drug Abuse, National Institutes of Health

  • Rong Xu, PhD, Case Western Reserve University School of Medicine, 1Center for Artificial Intelligence in Drug Discovery

United Kingdom to End Most COVID Restrictions

British Prime Minister Boris Johnson told Parliament members today that coronavirus passports and masking mandates will end by January 26 and that all other COVID restrictions would end by March 24.

In remarks to the House of Commons, the primary chamber of the British Parliament, Johnson called for an end to the nation’s “Plan B” COVID restrictions.

As Infections Recede U.K. to Repeal COVID Laws

Johnson made the announcement on the basis that COVID cases appeared to have peaked in England. Infection cases are also being dominated by the less lethal Omicron variant, against which current vaccines are less effective. His comments were met with cheers from Conservative benches.

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The United Kingdom reported more than 108,000 new positive Covid tests on Wednesday, compared to about 130,000 a week ago. Cases have been dropping most of this year.

Deaths and hospitalization rates have also fallen.

COVID Passports and Masking Requirements Will End

Johnson told lawmakers that the government would no longer enforce COVID passport or masking requirements in businesses or public spaces, including at schools.

The government is expected to announce rollbacks of other restrictions on travel and health care settings shortly.

Politics, Not Vaccines, May End COVID Era in Britain

Johnson made his comments to shore up waning political support due to his handling of the pandemic. Several political parties have called on his government to resign.

As he announced an end of the COVID era in Britain, Labour Party leaders, trade unions and certain doctors’ groups criticized Johnson’s plan even as opponents of the U.K.’s draconian restrictions supported him.

COVID Still Divides the World

The announcement comes at a time of widening divisions across the globe. Nations including ChinaAustraliaAustria and Germany appear to be embracing still more draconian vaccine mandates, masking requirements and restrictions on travel and movement within their borders. Meanwhile nations such as IsraelSpain and Cyprus have entertained easing COVID restrictions in recent weeks.

The United States is deeply fractured in its approach with the Supreme Court having recently struck down President Joe Biden’s vaccine mandates for business with a 100 employees or more even as it upheld mandates for federal health care workers. States and cities are also responding in piecemeal fashion to new pandemic developments, with some, including California and New York, persisting with tight restrictions and others, including Florida and Texas, easing COVID rules.

Britain’s course has had outsized impacts on global COVID responses from the start. As early as March 2020 models presented by Professor Neil Ferguson, head of the MRC GIDA team and director of the Abdul Latif Jameel Institute for Disease and Emergency Analytics (J-IDEA) steered the world toward a new complex of rules and restrictions that drove protesters to the streets and led billions to isolate in their homes and behind face masks.

Now that one of the pioneers of the global COVID regime has changed course, other nations across the world will likely reexamine their policies as well. Regardless of what governments decide the COVID era will have lasting impacts, globally, on democratic principles and more general matters of governance including notions of rule of law, individual liberty, due process and appropriate public health responses.

Studies Show Horrific Contaminations of PCR Test Swabs

Two additional studies by researchers in different countries show horrific contamination of PCR test swabs⏤produced by different manufacturers.

Last week I wrote about the horrific contamination of PCR test swabs discovered in testing products of a Chinese manufacturer.

To remind you, here is an electron microscope photograph of what is being inserted into the noses of those of us exposed to the Chinese manufacturer’s swabs. Be ready to be shocked.

This swab appears to be made of fiberglass. Or at least to have a fiberglass coating. This, of course, could rip, cut, and tear flesh, causing bleeding. Broken pieces could become lodged in the nose causing infection.

To determine if such contamination was related only to that one manufacturer, I searched for similar results for other swab products. And yes, diving into search, I again found something immediately that caught my eye.  

Additional frightening research findings by molecular chemistry and pathology experts. Here is the report. It relates to a South Korean manufacturer that provides much of the EU with PCR swabs.

This additional study concludes that material and chemical abnormalities in the material at the tip of the swab (produced by a South Korean manufacturer) are likely responsible for damage to the nasal passage, resulting in bleeding and other injuries. Here is part of this additional (second) study:

October 24, 2021 –

Undeclared Hazardous Components in Nasopharyngeal Test Swabs Used in Covid-19 PCR Tests

‘We tested two widely used nasopharyngeal test swabs used for COVID-19 PCR test sample collection by the SEM-EDS method. 

Scanning electron microscopic (SEM) analysis demonstrated fairly uniform artificial fibers that showed a great degree of heterogeneity in their internal composition. 

Elemental analysis by electron dispersion spectroscopy (EDS) revealed carbon, oxygen, nitrogen, aluminum, and silicon as main components at highly variable concentrations within the cross-sections of the fibers. 

In some spots, the concentrations of aluminum and silicon were as high as 7.25% and 14.06%, respectively. 

The base matrix appeared to be nylon with inorganic ingredients mixed in. Aluminum and silicon can both present health hazards, and this can explain the rapid-onset nasal bleed and strong and lasting adverse reactions reported by the tested individuals.”  

One of the striking things about the horrific test results is that they are basically the same as those of the Chinese product of which we reviewed the testing last week.

The manufacturers are in different countries and have no known public connections.

So how is it possible that the same results of dangerous contamination of a supposedly 100% nylon test material are the same?

One possibility that could be imagined is that the Korean company is purchasing the product in China and selling it as their own to the EU and other Western countries. No one is claiming this is happening, but it is a possibility.

Another possibility is that there is a supplier of this nylon material that supplies both the Chinese and Korean companies.

But whatever the cause of the contamination, it exists and is widespread.  

A third study clarifies that this is a rampant problem. In this study, a totally different set of contaminates was discovered in the swab collection material by a third manufacturer.

A Third Study

According to another independent test on PCR swabs in Slovakia, the material they found was Darpa patented hydrogel, lithium, and nylon. DARPA relates to materials normally used for military purposes.

Here is part of what this third test found:

” After spawning a mixture of nylon fiber fragments, Darpa Hydrogel remains on the nasal mucosa under the pituitary and pineal gland along with lithium. This mixture immediately reacts with living structures to form crystals that are directionally oriented to the pineal gland, which has its own electromagnetic field.

The shape of the crystals determines the type of hydrogel used. The crystals are conductive due to the lithium contained in it. The crystals can receive the signal from the transmitter to the cell and transmit signals from the cell to the transmitter. These are actually nano-antennas.”

According to the article, lithium, as well as aluminum and mercury (widely used in vaccines), are highly toxic to the pineal gland influence. In low doses, lithium blocks it, and in higher doses, it can completely destroy it.  

The study results continued:

” Darpa Hydrogel and lithium, block and destroy the pineal gland and cause the thinking person to become a controllable biorobot. A hydrogel is a carrier of an active substance, its task is to get the substance into the body at a pre-desired place.” – see shocking photos: Nutritruth.org.

Interestingly, Ivermectin which has been found to be an effective, safe treatment for Covid, dissolves the Hydrogen crystals.”

Conspiracy Theory?

A term used by the Fascistic Left to suppress what is often actually true!

The term “conspiracy theory” is a language weapon of the fascist Democrat Party and its media slaves, to silence what is often accurate information.

There have been occasional articles throughout the pandemic, about PCR swabs being used as a bioweapon to sicken enemies of whatever country was producing biologically infected swabs. In addition to biological infection, the “conspiracy theory” articles mentioned the presence of metallic micro-flakes as cutting edges. The purpose of which is to damage flesh, causing bleeding, infections, and possibly brain damage. And these “conspiracy theory” metallic micro flakes are actually appearing in the studies mentioned in this post.

The tested swabs are in use in the EU, and have the CE quality mark, as meeting EU standards. Which clearly, they do not.

It’s horrific to think of some of us who have stood in long lines to get PCR tests, that we were waiting in line for injury. The entire government pandemic narrative is warped. It’s time to break free.