COVID-19
New film ‘Epidemic of Fraud’ exposes massive COVID corruption
From LifeSiteNews
By Frank Wright
‘Epidemic of Fraud’ exposes the suppression of hydroxychloroquine, a potential solution to the COVID crisis, orchestrated by government entities including the FDA.
This month sees the release of a new film documenting the COVID regime. What is different about “Epidemic of Fraud” is the scope of corruption it exposes, reaching beyond the prohibition of genuinely safe and effective medicine, to massive financial and political motives to promote lockdowns and the dangerous “vaccines” instead.
John Davidson’s film begins with the scandalous campaign against hydroxychloroquine, a derivative of quinine, the naturally occurring wonder drug whose control has always been a matter of U.S. national security.
“This was the answer. This would have halted the pandemic.” So said Steven Hatfill – COVID adviser to President Donald Trump – in a segment in the film. He noted that “within a week or so, we had 62 million doses” of hydroxychloroquine.
He continued: “52 other countries have used it successfully to keep their pandemic – their hospital admissions under control”
So who decided to halt the Trump administration’s early treatment plan to administer a proven cure? As Davidson shows, “The idea to halt hydroxychloroquine came from the FDA.”
Davidson is far from alone in showing precisely who was responsible.
Dr. Robert Malone – ‘cause unknown’
Davidson, a committed Christian, began as a radio journalist, eventually moving to television and film production. He admits early in the film that he, too, promoted COVID measures, thinking he was providing a public service. It was the restrictions on hydroxychloroquine, he told LifeSiteNews, that “red-pilled” him.
Beginning in 2020, he spent the intervening years in piecing together a story which amounted to a massive fraud conducted on, and at the expense of, the American people.
His film makes extensive use of interview footage from the lockdown period, showing Dr. Robert Malone in 2021 explaining to Joe Rogan exactly who was behind the suppression of a cheap drug that could have stopped the pandemic in its tracks. It was, according to Malone, a “conspiracy between [the FDA’s] Janet Woodcock and Rick Bright to make it so that physicians could not administer hydroxychloroquine outside of the hospital.”
Rick Bright was demoted from his position as director of BARDA, the Biomedical Advanced Research and Development Authority, for smearing Trump’s recommendation of hydroxychloroquine as “dangerous.”
As to why the hydroxychloroquine restriction mattered, the truth of the claim against Bright, Malone went on:
Rick Bright in videotaped testimony has explicitly spoken about how they conspired to cook up a strategy to make it so that hydroxychloroquine could only be administered in the hospital – which by the way is too late for when [it] should be used.
Rogan asked Malone the obvious question – why did they do that?
“That is what is the unknown” replied Malone. “There are so many whys and hows – I like to say – there’s a stack of stuff that doesn’t make sense.”
Yet Davidson’s film makes a lot of sense of this seemingly senseless decision. Bright was championed as a heroic “whistleblower” for his leading role in the plan to deprive Americans of a safe and affordable remedy for COVID-19.
Bright’s ambitions are now global. He moved on to work as CEO of the Pandemic Prevention Institute at the Rockefeller Foundation in 2021, celebrating a new World Health Organization “Pandemic Intelligence Centre.” He also spoke at the 2024 World Economic Forum on a panel discussing the role of artificial intelligence in “future cures” and “rebuilding trust in a better tomorrow.”
Bright’s LinkedIn profile reads: “Exponential Transformation of Global Health & Healthcare (Changing the World).” His record leaves no doubt as to the nature of this better world he envisions for us all.
Bureaucrats v. The People
The film shows how Davidson contacted the FDA to submit a FOIA (Freedom of Information Act) request, to see communications between the two major decision makers – Rick Bright and Janet Woodcock.
In a phone call with the Food and Drug Administration, Davidson was told he would have to wait two years to see the data, due to a backlog of 1100 similar requests.
Davidson used his time to investigate the two decision makers whose actions led to a campaign of suppression of hydroxychloroquine that was so successful, that doctors could be ruined if they continued to prescribe it.
“If you use these drugs [in the U.S.] you probably will be fired” said one doctor, as the film documented how doctors in Australia’s Queensland faced imprisonment for prescribing “HCQ,” as hydroxychloroquine is known. As Congressman Jim Jordan points out later in the film, “Something has happened to prevent early treatment.”
The film shows Rep. Jordan speaking at a November 2020 hearing, saying these “logjams” have been created by officials to deny Americans and their elected officials access to the truth.
We should have the right to access this without the interference of bureaucrats at the FDA and CDC.
I can’t get it. Millions of Americans can’t get it because of the logjam created by bureaucrats.
Sen. Ron Johnson was accused the next month of “elevating fringe theories” to “question virus science” by the New York Times, who nonetheless quoted him as saying, “There’s a blackout on good information in social media and media. So people are being denied information to make intelligent choices themselves.”
This blackout was spearheaded by Dr. Antony Fauci, who said at the time that there was a “distinct anti-science flavor” to those questioning his promotion of “vaccines,” lockdowns, masks, and social distancing. Fauci said he effectively was “the science,” and the media played along.
“[T]hey get up and criticize science… but if they criticize me they are criticizing science – cause I represent science,” Fauci had stated.
It became “anti-science” to question anything about this epidemic of fraud. It also became nigh impossible to get any answers. Asking why led Davidson to a darker dimension which had a bearing on another widely censored subject – the 2020 presidential election.
Political pressure
Davidson points out that if the COVID pandemic continued, then the use of mail-in ballots in the presidential election would be permitted under lockdown conditions.
Secondly, he says there was considerable pressure to deprive Donald Trump of a “win,” with a coordinated media campaign caricaturizing the president as insane for recommending hydroxychloroquine. He was linked to the death of a man who drank fish tank cleaner, as the promotion of the “100% safe and effective” mRNA injections began to intensify.
With people locked indoors before their screens, this was the message many received about Trump, and the centuries-old remedy he had endorsed – months before they would vote for their new president.
Canada’s CBC published a news alert on their X (formerly Twitter) account in March 2020, reading, “Arizona man dead, woman in critical condition after ingesting chemical touted by U.S. President Donald Trump as potential COVID-19 treatment. ‘Don’t believe anything that the president says,’ woman tells NBC. ‘Call your doctor.’”
As Davidson shows, the information war against Trump and the proven safety of hydroxychloroquine was undertaken amid enormous pressures, both political and financial. If Trump won again, would he return to promoting a $20 per dose drug, against the novel “vaccines” and the deadly Remdesivir, which was $3000 per treatment? Davidson asks his audience:
With 11 trillion dollars on the line, and the risk of Trump being right – could you have said hydroxychloroquine works?
If Davidson’s cost estimate sounds fantastical, consider that in 2020 Harvard University estimated that the cost to the U.S. from COVID-19 might run to $16 trillion.
This appraisal was revisited in a study in May 2023. Undertaken by the University of Southern California, it showed that by the end of 2023, the total cost of the pandemic to the U.S. would already amount to $14 trillion.
Consider now that these costs, most of which arose from lockdown restrictions, could have been avoided. Now factor in the many vaccine injured and those who have “died suddenly,” along with care home deaths, ventilator deaths, and other iatrogenic fatalities arising from the use of drugs such as midazolam. This is where following the science has led us.
An out-of-patent medicine, cheaply available and known to be safe for centuries could have stopped it all.
John Wilkes Booth and quinine
The film covers the remarkable history of the naturally occurring antimalarial compound quinine, including the fascinating detail that John Wilkes Booth, Lincoln’s would-be assassin, had been “smuggling quinine to desperate families” across the rebel South. Lincoln had aimed to “create as many sick and dead Southern soldiers as possible” by blockading the distribution of quinine.
Davidson shows Lincoln’s northern blockade was just one example of the military dimension to the deliberate restriction of access to quinine, of which hydroxychloroquine is a modern derivative.
It is this which gives tonic water its distinctive tang, and for this reason the gin and tonic was widely consumed by the British in the tropics. Quinine has long been safe and effective in treating a variety of sicknesses, and is so vital that its stockpiling was ordered again by the U.S. government in 1946 – as Davidson shows. The military significance of the drug which could have saved America has a long heritage. Its restriction was described by Davidson as an arguable case of “biological warfare.” This is one further disturbing dimension to the true pandemic which blighted nations under Fauci’s lockdowns.
Epidemic fraud
The message of Davidson’s film is that something is seriously wrong with our world. This wrong is not restricted to the media, whose smear campaigns “gaslit” the public into compliance, leading them to take novel treatments whose manufacturers were indemnified from liability.
It extends beyond the intimidation of doctors and the reputational ruin those brave enough to speak out have suffered. Davidson’s film, a remarkable cinematic achievement for a man who made it largely alone in his garage, is a document which will embolden anyone who sees it against the corruption that has replaced public service at the highest levels.
The film can be understood as an insight into one of the most dedicated and successful acts of self-harm that a nation has ever undertaken. The United States government, its health officials, its captive media, and its trusted public health officials have destroyed public trust along with risking the health, lives, and livelihoods of millions of its citizens.
Davidson’s film deserves the widest possible audience, as it speaks beyond partisan antagonisms to reveal a systematic betrayal of the American public, coordinated through the channels of guidance and information that Americans expected to serve them – and not the powerful political and financial interests he exposes here.
The sickness he documents is not a lab-created virus. It is the capture of the free world by dark forces whose hunger for power and for profit will see them poison their own well.
Speaking to Davidson in an interview, LifeSiteNews asked what he thought the future might hold, as public awareness of the magnitude of the epidemic of fraud around COVID grows. His answer was inspirational.
People are coming together over this. I have met lawyers fighting for the vaccine-injured, brave doctors speaking out, and there is a real movement growing.
He finished with a striking image.
I think about David and Goliath a lot.
My film is like the stone that David fired from his sling. I have released the stone. It is up to God now where it finds its mark.
You can watch “Epidemic of Fraud” by completing an email registration on Davidson’s site “Broken Truth.”
Brownstone Institute
The Deplorable Ethics of a Preemptive Pardon for Fauci
From the Brownstone Institute
Anthony “I represent science” Fauci can now stand beside Richard “I am not a crook” Nixon in the history books as someone who received the poison pill of a preemptive pardon.
While Nixon was pardoned for specific charges related to Watergate, the exact crimes for which Fauci was pardoned are not specified. Rather, the pardon specifies:
Baseless and politically motivated investigations wreak havoc on the lives, safety, and financial security of targeted individuals and their families. Even when individuals have done nothing wrong – and in fact have done the right things – and will ultimately be exonerated, the mere fact of being investigated and prosecuted can irreparably damage reputations and finances.
In other words, the dying breath of the Biden administration appears to be pardoning Fauci for crimes he didn’t commit, which would seem to make a pardon null and void. The pardon goes further than simply granting clemency for crimes. Clemency usually alleviates the punishment associated with a crime, but here Biden attempts to alleviate the burden of investigations and prosecutions, the likes of which our justice system uses to uncover crimes.
It’s one thing to pardon someone who has been subjected to a fair trial and convicted, to say they have already paid their dues. Gerald Ford, in his pardon of Richard Nixon, admitted that Nixon had already paid the high cost of resigning from the highest office in the land. Nixon’s resignation came as the final chapter of prolonged investigations into his illegal and unpresidential conduct during Watergate, and those investigations provided us the truth we needed to know that Nixon was a crook and move on content that his ignominious reputation was carve d into stone for all of history.
Fauci, meanwhile, has evaded investigations on matters far more serious than Watergate. In 2017, DARPA organized a grant call – the PREEMPT call – aiming to preempt pathogen spillover from wildlife to people. In 2018 a newly formed collaborative group of scientists from the US, Singapore, and Wuhan wrote a grant – the DEFUSE grant – proposing to modify a bat sarbecovirus in Wuhan in a very unusual way. DARPA did not fund the team because their work was too risky for the Department of Defense, but in 2019 Fauci’s NIAID funded this exact set of scientists who never wrote a paper together prior or since. In late 2019, SARS-CoV-2 emerged in Wuhan with the precise modifications proposed in the DEFUSE grant submitted to PREEMPT.
It’s reasonable to be concerned that this line of research funded by Fauci’s NIAID may have caused the pandemic. In fact, if we’re sharp-penciled and honest with our probabilities, it’s likely beyond reasonable doubt that SARS-CoV-2 emerged as a consequence of research proposed in DEFUSE. What we don’t know, however, is whether the research proceeded with US involvement or not.
Congress used its constitutionally-granted investigation and oversight responsibilities to investigate and oversee NIAID in search of answers. In the process of these investigations, they found endless pages of emails with unjustified redactions, evidence that Fauci’s FOIA lady could “make emails disappear,” Fauci’s right-hand-man David Morens aided the DEFUSE authors as they navigated disciplinary measures at NIH and NIAID, and there were significant concerns that NIAID sought to obstruct investigations and destroy federal records.
Such obstructive actions did not inspire confidence in the innocence of Anthony Fauci or the US scientists he funded in 2019. On the contrary, Fauci testified twice under oath saying NIAID did not fund gain-of-function research of concern in Wuhan…but then we discovered a 2018 progress report of research NIAID funded in Wuhan revealing research they funded had enhanced the transmissibility of a bat SARS-related coronavirus 10,000 times higher than the wild virus. That is, indisputably, gain-of-function research of concern. Fauci thus lied to the American public and perjured himself in his testimony to Congress, and Senator Rand Paul (R-KY) has referred Fauci’s perjury charges to the Department of Justice.
What was NIAID trying to preempt with their obstruction of Congressional investigations? What is Biden trying to preempt with his pardon of Fauci? Why do we not have the 2019 NIAID progress report from the PI’s who submitted DEFUSE to PREEMPT and later received funding from NIAID?
It is deplorable for Biden to preemptively pardon Fauci on his last day in office, with so little known about the research NIAID funded in 2019 and voters so clearly eager to learn more. With Nixon’s preemptive pardon, the truth of his wrongdoing was known and all that was left was punishment. With Fauci’s preemptive pardon, the truth is not yet known, NIAID officials in Fauci’s orbit violated federal records laws in their effort to avoid the truth from being known, and Biden didn’t preemptively pardon Fauci to grant clemency and alleviate punishment, but to stop investigations and prosecutions the likes of which could uncover the truth.
I’m not a Constitutional scholar prepared to argue the legality of this maneuver, but I am an ethical human being, a scientist who contributed another grant to the PREEMPT call, and a scientist who helped uncover some of the evidence consistent with a lab origin and quantify the likelihood of a lab origin from research proposed in the DEFUSE grant. Any ethical human being knows that we need to know what caused the pandemic, and to deprive the citizenry of such information from open investigations of NIAID research in 2019 would be to deprive us of critical information we need to self-govern and elect people who manage scientific risks in ways we see fit. As a scientist, there are critical questions about bioattribution that require testing, and the way to test our hypotheses is to uncover the redacted and withheld documents from Fauci’s NIAID in 2019.
The Biden administration’s dying breath was to pardon Anthony Fauci not for the convictions for crimes he didn’t commit (?) but to avoid investigations that could be a reputational and financial burden for Anthony Fauci. A pardon to preempt an investigation is not a pardon; it is obstruction. The Biden administration’s dying breath is to obstruct our pursuit of truth and reconciliation on the ultimate cause of 1 million Americans’ dying breaths.
To remind everyone what we still need to know, it helps to look through the peephole of what we’ve already found to inspire curiosity about what else we’d find if only the peephole could be widened. Below is one of the precious few emails investigative journalists pursuing FOIAs against NIAID have managed to obtain from the critical period when SARS-CoV-2 is believed to have emerged. The email connects DEFUSE PI’s Peter Daszak (EcoHealth Alliance), Ralph Baric (UNC), Linfa Wang (Duke-NUS), Ben Hu (Wuhan Institute of Virology), Shi ZhengLi (Wuhan Institute of Virology) and others in October 2019. The subject line “NIAID SARS-CoV Call – October 30/31” connects these authors to NIAID.
It is approximately in that time range – October/November 2019 – when SARS-CoV-2 is hypothesized to have entered the human population in Wuhan. When it emerged, SARS-CoV-2 was unique among sarbecoviruses in having a furin cleavage site, as proposed by these authors in their 2019 DEFUSE grant. Of all the places the furin cleavage site could be, the furin cleavage site of SARS-CoV-2 was in the S1/S2 junction of the Spike protein, precisely as proposed by these authors.
In order to insert a furin cleavage site in a SARS-CoV, however, the researchers would’ve needed to build a reverse genetic system, i.e. a DNA copy of the virus. SARS-CoV-2 is unique among coronaviruses in having exactly the fingerprint we would expect from reverse genetic systems. There is an unusual even spacing in the cutting/pasting sites for the enzymes BsaI and BsmBI and an anomalous hot-spot of silent mutations in precisely these sites, exactly as researchers at the Wuhan Institute of Virology have done for other coronavirus reverse genetic systems. The odds of such an extreme synthetic-looking pattern occurring in nature are, conservatively, about 1 in 50 billion.
The virus did not emerge in Bangkok, Hanoi, Bago, Kunming, Guangdong, or any of the myriad other places with similar animal trade networks and greater contact rates between people and sarbecovirus reservoirs. No. The virus emerged in Wuhan, the exact place and time one would expect from DEFUSE.
With all the evidence pointing the hounds towards NIAID, it is essential for global health security that we further investigate the research NIAID funded in 2019. It is imperative for our constitutional democracy, for our ability to self-govern, that we learn the truth. The only way to learn the truth is to investigate NIAID, the agency Fauci led for 38 years, the agency that funded gain-of-function research of concern, the agency named in the October 2019 call by DEFUSE PI’s, the agency that funded this exact group in 2019.
A preemptive pardon prior to the discovery of truth is a fancy name for obstruction of justice. The Biden administration’s dying breath must be challenged, and we must allow Congress and the incoming administration to investigate the possibility that Anthony Fauci’s NIAID-supported research caused the Covid-19 pandemic.
Republished from the author’s Substack
COVID-19
BREAKING: Days before Trump Inauguration HHS fires doctor in charge of gain of function research project
Dr. Daszak will likely be protected by the DoD & CIA from additional penalties.
By John Leake
HHS Formally Debars EcoHealth Alliance, President Peter Daszak Fired.
On January 17, 2025—just three days before President Trump is to be sworn in—Congress issued a press release with the following statement:
Today, after an eight-month investigation, the U.S. Department of Health and Human Services (HHS) cut off all funding and formally debarred EcoHealth Alliance Inc. (EcoHealth) and its former President, Dr. Peter Daszak, for five years based on evidence uncovered by the Select Subcommittee on the Coronavirus Pandemic.
As far as I can tell, the New York Times did not report this story, though the New York Post did.
More interesting than the superficial news reporting is the HHS ACTION REFERRAL MEMORANDUM recommending that Dr. Peter Daszak be barred from participating in United States Federal Government procurement and nonprocurement programs.
The Memorandum also states:
Dr. Peter Daszak was the President and Chief Executive Officer of EHA from 2009 until his termination, effective January 6, 2025. Dr. Daszak was the Project Director (PD)/Principal Investigator (PI) for Grant Number 1R01AI110964-01.
I am not sure what to make of this document, which is written in such an arcane and convoluted style that it challenges the attention span of even the most focused reader.
I have been researching this story for four years, and I found the following paragraphs the most intriguing:
9. In a letter dated May 28, 2016, the NIAID contacted EHA concerning possible GoF research based on information submitted in its most recent Year 2 RPPR. The NIAID notified EHA that GoF research conducted under Grant Number 5R01AI110964-03 would be subject to the October 17, 2014, United States Federal Government funding pause, and that per the funding pause announcement, new United States Federal Government funding would not be released for GoF research projects that may be reasonably anticipated to confer attributes to influenza, MERS, or SARS viruses such that the virus would have enhanced pathogenicity and/or transmissibility in mammals via the respiratory route. In the letter, the NIAID requested that EHA provide a determination within 15 days of the date of the letter as to whether EHA’s research under Grant Number 5R01AI110964-03 did or did not include GoF work subject to the funding pause.
10. In a letter dated June 8, 2016, EHA provided a response to the NIAID’s May 28, 2016 letter. EHA explained that the goal of its proposed work was to construct MERS and MERS-like chimeric CoVs in order to understand the potential origins of MERSCoV in bats by studying bat MERS-like CoVs in detail. EHA stated that it believed it was highly unlikely that the proposed work would have any pathogenic potential, but that should any of these recombinants show evidence of enhanced virus growth greater than certain specified benchmarks involving log growth increases, or grow more efficiently in human airway epithelial cells, EHA would immediately: (1) stop all experiments with the mutant, (2) inform the NIAID Program Officer of these results, and (3) participate in decision-making trees to decide appropriate paths forward.
11. Based on the information provided by EHA, the NIAID concluded that the proposed work was not subject to the GoF research pause. In a letter dated July 7, 2016, however, the NIAID informed EHA that should any of the MERS-like or SARS-like chimeras generated under the grant show evidence of enhanced virus growth greater than 1 log over the parental backbone strain, EHA must stop all experiments with these viruses and provide the NIAID Program Officer and Grants Management Specialist, and WIV Institutional Biosafety Committee, with the relevant data and information related to these unanticipated outcomes.
Note that various statements in the above paragraphs are inconsistent with what Baric et al. state in their 2015 paper A SARS-like cluster of circulating bat coronavirus shows potential for human emergence—a research paper funded by the NIAID EcoHealth Grant “Understanding the Risk of Bat Coronavirus Emergence.”
As the authors state in the section on Biosafety and biosecurity:
Reported studies were initiated after the University of North Carolina Institutional Biosafety Committee approved the experimental protocol (Project Title: Generating infectious clones of bat SARS-like CoVs; Lab Safety Plan ID: 20145741; Schedule G ID: 12279). These studies were initiated before the US Government Deliberative Process Research Funding Pause on Selected Gain-of-Function Research Involving Influenza, MERS and SARS Viruses (http://www.phe.gov/s3/
dualuse/Documents/gain-of- function.pdf). This paper has been reviewed by the funding agency, the NIH. Continuation of these studies was requested, and this has been approved by the NIH.
As I noted in my series of essays titled The Great SARS-CoV-2 Charade, one of the silliest lies told by Dr. Anthony Fauci has been his insistence that NIAID did not approve Gain-of-Function work by EcoHealth.
Fauci has repeatedly asserted this in a loud and vexed tone, as though he is outraged by the mere proposition. And yet, Ralph Baric and his colleagues—including Zhengli-Li Shi at the Wuhan Institute of Virology—plainly state in their 2015 paper that their Gain-of-Function experiments, performed in Baric’s UNC lab and Zhengli-Li Shi’s lab in Wuhan, were grandfathered in, given that they were funded before the 2014 Pause.
Another statement (in paragraph 11 of the recent HHS Action Referral Memo) that deserves special scrutiny is the following:
In a letter dated July 7, 2016, however, the NIAID informed EHA that should any of the MERS-like or SARS-like chimeras generated under the grant show evidence of enhanced virus growth greater than 1 log over the parental backbone strain, EHA must stop all experiments with these viruses and provide the NIAID Program Officer and Grants Management Specialist, and WIV Institutional Biosafety Committee, with the relevant data and information related to these unanticipated outcomes.
Again, it’s tough to interpret this statement, given that Baric et al. had, by the own admission, already generated chimeras that “replicate efficiently in primary human airway cells and achieve in vitro titers equivalent to epidemic strains of SARS-CoV.”
Let’s review what Baric et al. state in their Abstract about the functionality of the chimeric virus (named SHCOI4-MA15) they claimed to have generated. Using humanized mice (genetically modified to have primary human airway cells) as their experimental animals, the authors state:
Using the SARS-CoV reverse genetics system2, we generated and characterized a chimeric virus expressing the spike of bat coronavirus SHC014 in a mouse-adapted SARS-CoV backbone.
The results indicate that group 2b viruses encoding the SHC014 spike in a wild-type backbone can efficiently use multiple orthologs of the SARS receptor human angiotensin converting enzyme II (ACE2), replicate efficiently in primary human airway cells and achieve in vitro titers equivalent to epidemic strains of SARS-CoV. Additionally, in vivo experiments demonstrate replication of the chimeric virus in mouse lung with notable pathogenesis.
To this day, no legal authority that I am aware of has investigated the question: What became of the the chimeras SHC014-MA15 and WIV1-MA15? The latter chimera was documented by Baric et al. in their March 2016 paper titled SARS-like WIV1-CoV poised for human emergence—a chimera “that replaced the SARS spike with the WIV1 spike within the mouse-adapted backbone.”
What did the Wuhan Institute of Virology do with these chimeras? Did its researchers continue to modify and experiment with these chimeras?
Another exceedingly silly claim made by U.S. government officials—including members of Congress—is that the true origin of SARS-CoV-2 is likely to remain a mystery, given that the Chinese government and military will almost certainly never agree to perform a full and transparent investigation of their Wuhan Institute of Virology.
What did the U.S. government expect when it agreed to share cutting edge American biotechnology with the Wuhan Institute of Virology, which has long been known to be run by the Chinese military?
One grows weary of our U.S. government officials evading responsibility by pretending to be imbeciles or by revealing themselves to be true imbeciles.
If you found this post informative, please consider becoming a paid subscriber to our Substack. Penetrating the smoke and mirror show performed by the abominable U.S. government requires a great deal of time and effort.
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