Brownstone Institute
How Government and Big Tech Colluded to Usurp Constitutional rights
From the Brownstone Institute
BY
“It is also axiomatic that a state may not induce, encourage or promote private persons to accomplish what it is constitutionally forbidden to accomplish.” ~ Norwood v. Harrison (1973).
Fifty years ago, the Supreme Court held that the U.S. Government cannot coerce private parties to violate citizens’ constitutionally protected liberties. Under the guise of Covid responses, government officials defied this principle to strip Americans of their rights.
Behind Covid’s public spectacles – the memorable headlines of forced church closings, house arrest edicts, playground prohibitions, and bans on “unnecessary walking” – there was a coordinated effort to overthrow constitutional liberties.
Bureaucrats, federal officers, and elected officials colluded with Big Tech firms to accomplish unconstitutional aims. In doing so, they augmented government power and enriched Silicon Valley companies.
A federal-corporate collusion supplanted the American system of separation of powers and individual rights. This coup d’état usurped the Constitution and created a new ruling order of suppression and surveillance.
Suppression, Censorship, and the First Amendment
“Government has no power to restrict expression because of its message, its ideas, its subject matter or its content,” the Supreme Court decided in Ashcroft v. ACLU (2002). Yet, the Biden White House and the federal government seized that power under the shadow of Covid. They coerced, colluded, and encouraged social media companies to suppress speech that deviated from their preferred messaging.
The White House’s conduct in July 2021 exemplified this behavior. Publicly, officials launched a pressure campaign; privately, they conducted a direct censorship operation.
On July 15, 2021, White House Press Secretary Jen Psaki discussed social media “disinformation” related to Covid-19 at her press briefing. “Facebook needs to move more quicky to remove harmful, violative posts,” she told reporters.
Her boss, President Joe Biden, spoke with the press the following day. Discussing social media companies, he remarked, “They’re killing people.”
Biden later clarified his remarks, explaining that he was advocating for censorship, not making personal attacks. “My hope is that Facebook, instead of taking it personally that somehow I’m saying ‘Facebook is killing people,’ that they would do something about the misinformation,” he explained.
That week, White House Communications Director Kate Bedingfield appeared on MSNBC and said that social media “should be held accountable” and reiterated President Biden’s support for private actors to restrict the speech of journalists, advocates, and citizens.
Privately, government officials called for direct censorship of American citizens and journalists.
Twitter worked with the government to stifle criticism of the Biden administration related to Covid. For example, White House officials met with Twitter content moderators in April 2021 to coordinate censorship initiatives. White House officials specifically pressed Twitter on “why Alex Berenson [a journalist] hasn’t been kicked off from the platform.”
White House senior adviser Andy Slavitt continued to encourage Twitter to remove Berenson from the platform, and his efforts succeeded when Berenson received a “permanent ban” in August 2021, just weeks after the White House’s public pressure campaign.
White House officials encouraged Big Tech groups to censor Robert F. Kennedy Jr. and Tucker Carlson for questioning vaccine efficacy. White House Director of Digital Strategy Rob Flaherty demanded to know why Facebook had not removed a video of Carlson reporting the announcement that Johnson & Johnson’s vaccine was linked to blood clots.
In January 2023, Reason revealed internal Facebook emails concerning the federal government’s campaign to censor users that deviated from Covid orthodoxy.
Robby Soave explains:
Facebook routinely asked the government to vet specific claims, including whether the virus was “man-made” rather than zoonotic in origin. (The CDC responded that a man-made origin was “technically possible” but “extremely unlikely.”) In other emails, Facebook asked: “For each of the following claims, which we’ve recently identified on the platform, can you please tell us if: the claim is false; and, if believed, could this claim contribute to vaccine refusals?”
These initiatives stifled dissent by infringing on American citizens’ speech; in doing so, they stripped millions of Americans of their First Amendment right to receive information.
In Martin v. City of Struthers (1941), Justice Hugo Black wrote that the First Amendment “embraces the right to distribute literature, and necessarily protects the right to receive it.” Nearly thirty years later, Justice Thurgood Marshall wrote, “it is now well established that the Constitution protects the right to receive information and ideas” in Stanley v. Georgia.
In defiance of this precedent, bureaucrats specifically sought to interfere with citizens’ right to hear criticism of government Covid policy. In his demands to Facebook regarding Carlson’s coverage of the J&J vaccine, Flaherty wrote, “There’s 40,000 shares on the video. Who is seeing it now? How many?”
Flaherty’s censorship pressure continued, “How was this not violative… What exactly is the rule for removal vs. demoting?”
Republican state attorneys general have sued the Biden administration for allegedly violating the First Amendment in its censorship promotion. Their case – Schmitt v. Biden – has uncovered communications between the Biden White House and social media companies.
The emails discovered in the case reveal an ongoing collusion to stifle dissent. Over fifty government bureaucrats, twelve federal agencies, and representatives from companies including Google, Twitter, and Facebook worked together to coordinate censorship efforts.
For example, Facebook employees met with officials at the Department of Health and Human Services the week after President Biden accused the company of “killing people.” A Facebook executive followed up with the HHS officials after the meeting:
“I wanted to make sure you saw the steps we took just this past week to adjust policies on what we are removing with respect to misinformation, as well as steps taken to further address the ‘disinfo dozen’: we removed 17 additional Pages, Groups and Instagram accounts tied to the disinfo dozen (so a total of 39 Profiles, Pages, Groups and IG accounts deleted thus far, resulting in every member of the disinfo dozen having had at least one such entity removed).”
In Bantam Books v. Sullivan (1963), the Court ruled that Rhode Island violated the First Amendment when a state commission advised book distributors against publishing certain content. In a concurring opinion, Justice Douglas wrote, “the censor and First Amendment rights are incompatible.”
Despite this constitutional incompatibility, the government deliberately and repeatedly encouraged and coerced private companies into censoring Americans’ speech.
Meanwhile, the fourth estate actively participated and profited from the censorship regime.
Amidst its efforts to censor dissent, the federal government siphoned tax dollars to media networks – including CNN, Fox News, and The Washington Post – to promote its official narrative. The US Department of Health and Human Services paid media outlets $1 billion to “strengthen vaccine confidence” in 2021 as part of a “comprehensive media campaign.”
At the same time, legacy media outlets like The Washington Post, The BBC, Reuters, and ABC partnered with Google, YouTube, Meta, and Twitter in the “Trusted News Initiative” to coordinate censorship initiatives. In “The Twitter Files,” journalist Matt Taibbi revealed that these tech firms held “regular meetings” – often with government officials – to discuss efforts to suppress speech critical of government narratives.
In summary, the government cannot restrict speech based on content, cannot decide what information a citizen can obtain, cannot advise private companies against publishing speech, and cannot use private entities to encourage unconstitutional aims. Yet our government launched a coordinated campaign, publicly and privately, to augment its powers and suppress citizens’ speech.
Surveillance. General Warrants, and the Fourth Amendment
In addition to suppressing dissent, the federal government’s Covid response usurped the protections of the Fourth Amendment in its partnership with Big Tech data brokers.
The Fourth Amendment guarantees citizens the right to be free from unreasonable government searches and seizures. Designed in response to the British practice of “general warrants,” the Framers sought to end a police system that provided the government nearly unrestrained access to searching colonists, their homes, and their belongings.
Since its ratification in 1791, the Supreme Court has maintained that technological advancements do not diminish the right of citizens to be secure from unreasonable searches and seizures.
For example, in Kyllo v. United States (2001), the Court ruled that the use of thermal imagery to search a home violated the Fourth Amendment. Chief Justice Roberts later explained that Government – absent a warrant – “could not capitalize” on new technology to strip citizens’ Fourth Amendment rights.
In 2012, a unanimous Court ruled that warrantless GPS tracking violated the defendant’s Fourth Amendment rights in United States v. Jones.
Six years later, the Court again ruled that the Government violated a defendant’s Fourth Amendment rights when it tracked a suspect by acquiring his cell phone location data from his wireless carrier.
In that case – Carpenter v. United States – Chief Justice Roberts wrote that the Fourth Amendment’s “basic purpose” is to “safeguard the privacy and security of individuals against arbitrary invasions by government officials.”
During Covid, however, the United States government violated these legal holdings. Despite repeated rulings that the Government cannot use new technologies to infringe Fourth Amendment rights and clear precedent regarding the use of GPS and cell phone location data, the CDC used taxpayer funds to purchase Americans’ cell phone data from data broker SafeGraph.
In May 2022, Vice revealed that the CDC used cell phone data to track the location of tens of millions of Americans during Covid.
At first, the agency used this data to track compliance with lockdown orders, vaccine promotions, attendance at churches, and other Covid-related initiatives. Additionally, the agency explained that the “mobility data” will be available for further “agency-wide use” and “numerous CDC priorities.”
SafeGraph sold this information to federal bureaucrats, who then used the data to spy on millions of Americans’ behavior, including where they visited and whether they complied with house arrest orders. This created a digital “general warrant” unshackled from Constitutional restraints.
In other words, big tech firms profited from surreptitious schemes in which the U.S. Government used taxpayer dollars to violate the Fourth Amendment rights of the citizens that fund their operations. Unelected officials at the CDC then tracked Americans’ movements, religious observances, and medical activity.
A similar process occurred at the state level.
In Massachusetts, the state Department of Public Health worked with Google to secretly install Covid-tracing software on citizens’ smartphones. The public-private partnership created “MassNotify,” an app that tracks and traces people’s locations. The program appeared on citizens’ phones without their consent.
Robert Wright, a Massachusetts resident, and Johnny Kula, a New Hampshire resident who commutes to Massachusetts to work every day, have brought a legal action against the state. “Conspiring with a private company to hijack residents’ smartphones without the owners’ knowledge or consent is not a tool that the Massachusetts Department of Public Health may lawfully employ in its efforts to combat COVID-19,” they say in their complaint.
Public officials also used citizens’ GPS data to support their election campaigns in 2020. Voter analytics firm PredictWise boasted that it used “nearly 2 billion GPS pings” from Americans’ cell phones to assign citizens a “COVID-19 decree violation” score and a “COVID-19 concern” score.
PredictWise explained that the Arizona Democratic Party used these “scores” and collections of personal data to influence voters to support US Senator Mark Kelly. The firm’s clients include the Democratic parties of Florida, Ohio, and South Carolina.
Politicians and government agencies repeatedly and deliberately augmented their power by tracking their citizens and thus depriving them of their Fourth Amendment rights. They then analyzed that information, assigned citizens compliance “scores,” and used the spyware to manipulate voters to maintain their positions of authority.
In effect, government forces used Covid as a pretext to return to the system of general warrants that the Framers designed the Fourth Amendment to abolish. Government officials gained access to citizens’ movements, locations, and travel patterns, and they used the citizens’ tax dollars to do it.
The collusion of government and corporate power siphoned millions of dollars from taxpayers while abolishing the Fourth Amendment safeguards that protect citizens against arbitrary invasions by government officials.
In 1975, Senator Frank Church led a government investigation into intelligence agencies’ domestic spy programs that targeted groups including anti-war protestors and civil rights leaders. Senator Church, speaking of the agencies’ covert capability nearly 50 years ago, warned, “That capability at any time could be turned around on the American people, and no American would have any privacy left, such is the capability to monitor everything: telephone conversations, telegrams, it doesn’t matter. There would be no place to hide.”
Not only did the government turn its capability on the American people, but it recruited the most powerful information companies in the history of the world to advance its agenda, leaving American citizens poorer, stripped of their rights, and left with no place to hide.
How did it happen here?
Most of these Constitutional violations will never have their day in court. In addition to stripping Americans of their rights, the ruling class has insulated Covid’s hegemonic forces from legal liability.
No matter the result of the ongoing cases, including Schmidt v. Biden and Wright v. Mass. Department of Public Health – the questions loom: How did we lose our Bill of Rights so quickly? How did it happen here?
Justice Antonin Scalia noted that the Bill of Rights cannot serve as a safeguard against tyranny on its own. “If you think a bill of rights is what sets us apart, you’re crazy,” he said. “Every banana republic in the world has a bill of rights.”
The key to safeguarding liberty, according to Scalia, is the separation of powers.
Commenting on the Constitution of the Soviet Union’s extensive guarantees of freedoms of speech, assembly, political affiliation, religion, and conscience, Scalia wrote:
“They were not worth the paper they were printed on, as are the human rights guarantees of a large number of still-extant countries governed by Presidents-for-life. They are what the Framers of our Constitution called ‘parchment guarantees,’ because the real constitutions of those countries—the provisions that establish the institutions of government—do not prevent the centralization of power in one man or one party, thus enabling the guarantees to be ignored. Structure is everything.”
Our Constitution created a structure of government with multiple levels of separation of powers. But, to the detriment of Americans’ liberties, the federal government and Big Tech supplanted that structure with a federal-corporate partnership devoid of constitutional restraints.
Georgetown Law Professor Randy Barnett describes the Constitution as “the law that governs those who govern us.” But those who govern us deliberately disregarded constraints on their own authority and led a coup against their citizens in partnership with Big Tech.
Covid served a pretext for a convergence of power that left our Bill of Rights as little more than a “parchment guarantee.”
Brownstone Institute
FDA Exposed: Hundreds of Drugs Approved without Proof They Work

From the Brownstone Institute
By
The US Food and Drug Administration (FDA) has approved hundreds of drugs without proof that they work—and in some cases, despite evidence that they cause harm.
That’s the finding of a blistering two-year investigation by medical journalists Jeanne Lenzer and Shannon Brownlee, published by The Lever.
Reviewing more than 400 drug approvals between 2013 and 2022, the authors found the agency repeatedly ignored its own scientific standards.
One expert put it bluntly—the FDA’s threshold for evidence “can’t go any lower because it’s already in the dirt.”
A System Built on Weak Evidence
The findings were damning—73% of drugs approved by the FDA during the study period failed to meet all four basic criteria for demonstrating “substantial evidence” of effectiveness.
Those four criteria—presence of a control group, replication in two well-conducted trials, blinding of participants and investigators, and the use of clinical endpoints like symptom relief or extended survival—are supposed to be the bedrock of drug evaluation.
Yet only 28% of drugs met all four criteria—40 drugs met none.
These aren’t obscure technicalities—they are the most basic safeguards to protect patients from ineffective or dangerous treatments.
But under political and industry pressure, the FDA has increasingly abandoned them in favour of speed and so-called “regulatory flexibility.”
Since the early 1990s, the agency has relied heavily on expedited pathways that fast-track drugs to market.
In theory, this balances urgency with scientific rigour. In practice, it has flipped the process. Companies can now get drugs approved before proving that they work, with the promise of follow-up trials later.
But, as Lenzer and Brownlee revealed, “Nearly half of the required follow-up studies are never completed—and those that are often fail to show the drugs work, even while they remain on the market.”
“This represents a seismic shift in FDA regulation that has been quietly accomplished with virtually no awareness by doctors or the public,” they added.
More than half the approvals examined relied on preliminary data—not solid evidence that patients lived longer, felt better, or functioned more effectively.
And even when follow-up studies are conducted, many rely on the same flawed surrogate measures rather than hard clinical outcomes.
The result: a regulatory system where the FDA no longer acts as a gatekeeper—but as a passive observer.
Cancer Drugs: High Stakes, Low Standards
Nowhere is this failure more visible than in oncology.
Only 3 out of 123 cancer drugs approved between 2013 and 2022 met all four of the FDA’s basic scientific standards.
Most—81%—were approved based on surrogate endpoints like tumour shrinkage, without any evidence that they improved survival or quality of life.
Take Copiktra, for example—a drug approved in 2018 for blood cancers. The FDA gave it the green light based on improved “progression-free survival,” a measure of how long a tumour stays stable.
But a review of post-marketing data showed that patients taking Copiktra died 11 months earlier than those on a comparator drug.
It took six years after those studies showed the drug reduced patients’ survival for the FDA to warn the public that Copiktra should not be used as a first- or second-line treatment for certain types of leukaemia and lymphoma, citing “an increased risk of treatment-related mortality.”
Elmiron: Ineffective, Dangerous—And Still on the Market
Another striking case is Elmiron, approved in 1996 for interstitial cystitis—a painful bladder condition.
The FDA authorized it based on “close to zero data,” on the condition that the company conduct a follow-up study to determine whether it actually worked.
That study wasn’t completed for 18 years—and when it was, it showed Elmiron was no better than placebo.
In the meantime, hundreds of patients suffered vision loss or blindness. Others were hospitalized with colitis. Some died.
Yet Elmiron is still on the market today. Doctors continue to prescribe it.
“Hundreds of thousands of patients have been exposed to the drug, and the American Urological Association lists it as the only FDA-approved medication for interstitial cystitis,” Lenzer and Brownlee reported.
“Dangling Approvals” and Regulatory Paralysis
The FDA even has a term—”dangling approvals”—for drugs that remain on the market despite failed or missing follow-up trials.
One notorious case is Avastin, approved in 2008 for metastatic breast cancer.
It was fast-tracked, again, based on ‘progression-free survival.’ But after five clinical trials showed no improvement in overall survival—and raised serious safety concerns—the FDA moved to revoke its approval for metastatic breast cancer.
The backlash was intense.
Drug companies and patient advocacy groups launched a campaign to keep Avastin on the market. FDA staff received violent threats. Police were posted outside the agency’s building.
The fallout was so severe that for more than two decades afterwards, the FDA did not initiate another involuntary drug withdrawal in the face of industry opposition.
Billions Wasted, Thousands Harmed
Between 2018 and 2021, US taxpayers—through Medicare and Medicaid—paid $18 billion for drugs approved under the condition that follow-up studies would be conducted. Many never were.
The cost in lives is even higher.
A 2015 study found that 86% of cancer drugs approved between 2008 and 2012 based on surrogate outcomes showed no evidence that they helped patients live longer.
An estimated 128,000 Americans die each year from the effects of properly prescribed medications—excluding opioid overdoses. That’s more than all deaths from illegal drugs combined.
A 2024 analysis by Danish physician Peter Gøtzsche found that adverse effects from prescription medicines now rank among the top three causes of death globally.
Doctors Misled by the Drug Labels
Despite the scale of the problem, most patients—and most doctors—have no idea.
A 2016 survey published in JAMA asked practising physicians a simple question—what does FDA approval actually mean?
Only 6% got it right.
The rest assumed that it meant the drug had shown clear, clinically meaningful benefits—such as helping patients live longer or feel better—and that the data was statistically sound.
But the FDA requires none of that.
Drugs can be approved based on a single small study, a surrogate endpoint, or marginal statistical findings. Labels are often based on limited data, yet many doctors take them at face value.
Harvard researcher Aaron Kesselheim, who led the survey, said the results were “disappointing, but not entirely surprising,” noting that few doctors are taught about how the FDA’s regulatory process actually works.
Instead, physicians often rely on labels, marketing, or assumptions—believing that if the FDA has authorized a drug, it must be both safe and effective.
But as The Lever investigation shows, that is not a safe assumption.
And without that knowledge, even well-meaning physicians may prescribe drugs that do little good—and cause real harm.
Who Is the FDA Working for?
In interviews with more than 100 experts, patients, and former regulators, Lenzer and Brownlee found widespread concern that the FDA has lost its way.
Many pointed to the agency’s dependence on industry money. A BMJ investigation in 2022 found that user fees now fund two-thirds of the FDA’s drug review budget—raising serious questions about independence.

Yale physician and regulatory expert Reshma Ramachandran said the system is in urgent need of reform.
“We need an agency that’s independent from the industry it regulates and that uses high-quality science to assess the safety and efficacy of new drugs,” she told The Lever. “Without that, we might as well go back to the days of snake oil and patent medicines.”
For now, patients remain unwitting participants in a vast, unspoken experiment—taking drugs that may never have been properly tested, trusting a regulator that too often fails to protect them.
And as Lenzer and Brownlee conclude, that trust is increasingly misplaced.
- Investigative report by Jeanne Lenzer and Shannon Brownlee at The Lever [link]
- Searchable public drug approval database [link]
- See my talk: Failure of Drug Regulation: Declining standards and institutional corruption
Republished from the author’s Substack
Brownstone Institute
Anthony Fauci Gets Demolished by White House in New Covid Update

From the Brownstone Institute
By
Anthony Fauci must be furious.
He spent years proudly being the public face of the country’s response to the Covid-19 pandemic. He did, however, flip-flop on almost every major issue, seamlessly managing to shift his guidance based on current political whims and an enormous desire to coerce behavior.
Nowhere was this more obvious than his dictates on masks. If you recall, in February 2020, Fauci infamously stated on 60 Minutes that masks didn’t work. That they didn’t provide the protection people thought they did, there were gaps in the fit, and wearing masks could actually make things worse by encouraging wearers to touch their face.
Just a few months later, he did a 180, then backtracked by making up a post-hoc justification for his initial remarks. Laughably, Fauci said that he recommended against masks to protect supply for healthcare workers, as if hospitals would ever buy cloth masks on Amazon like the general public.
Later in interviews, he guaranteed that cities or states that listened to his advice would fare better than those that didn’t. Masks would limit Covid transmission so effectively, he believed, that it would be immediately obvious which states had mandates and which didn’t. It was obvious, but not in the way he expected.

And now, finally, after years of being proven wrong, the White House has officially and thoroughly rebuked Fauci in every conceivable way.
White House Covid Page Points Out Fauci’s Duplicitous Guidance
A new White House official page points out, in detail, exactly where Fauci and the public health expert class went wrong on Covid.
It starts by laying out the case for the lab-leak origin of the coronavirus, with explanations of how Fauci and his partners misled the public by obscuring information and evidence. How they used the “FOIA lady” to hide emails, used private communications to avoid scrutiny, and downplayed the conduct of EcoHealth Alliance because they helped fund it.
They roast the World Health Organization for caving to China and attempting to broaden its powers in the aftermath of “abject failure.”
“The WHO’s response to the COVID-19 pandemic was an abject failure because it caved to pressure from the Chinese Communist Party and placed China’s political interests ahead of its international duties. Further, the WHO’s newest effort to solve the problems exacerbated by the COVID-19 pandemic — via a “Pandemic Treaty” — may harm the United States,” the site reads.
Social distancing is criticized, correctly pointing out that Fauci testified that there was no scientific data or evidence to support their specific recommendations.
“The ‘6 feet apart’ social distancing recommendation — which shut down schools and small business across the country — was arbitrary and not based on science. During closed door testimony, Dr. Fauci testified that the guidance ‘sort of just appeared.’”
There’s another section demolishing the extended lockdowns that came into effect in blue states like California, Illinois, and New York. Even the initial lockdown, the “15 Days to Slow the Spread,” was a poorly reasoned policy that had no chance of working; extended closures were immensely harmful with no demonstrable benefit.
“Prolonged lockdowns caused immeasurable harm to not only the American economy, but also to the mental and physical health of Americans, with a particularly negative effect on younger citizens. Rather than prioritizing the protection of the most vulnerable populations, federal and state government policies forced millions of Americans to forgo crucial elements of a healthy and financially sound life,” it says.
Then there’s the good stuff: mask mandates. While there’s plenty more detail that could be added, it’s immensely rewarding to see, finally, the truth on an official White House website. Masks don’t work. There’s no evidence supporting mandates, and public health, especially Fauci, flip-flopped without supporting data.
“There was no conclusive evidence that masks effectively protected Americans from COVID-19. Public health officials flipped-flopped on the efficacy of masks without providing Americans scientific data — causing a massive uptick in public distrust.”
This is inarguably true. There were no new studies or data justifying the flip-flop, just wishful thinking and guessing based on results in Asia. It was an inexcusable, world-changing policy that had no basis in evidence, but was treated as equivalent to gospel truth by a willing media and left-wing politicians.
Over time, the CDC and Fauci relied on ridiculous “studies” that were quickly debunked, anecdotes, and ever-shifting goal posts. Wear one cloth mask turned to wear a surgical mask. That turned into “wear two masks,” then wear an N95, then wear two N95s.
All the while ignoring that jurisdictions that tried “high-quality” mask mandates also failed in spectacular fashion.

And that the only high-quality evidence review on masking confirmed no masks worked, even N95s, to prevent Covid transmission, as well as hearing that the CDC knew masks didn’t work anyway.
The website ends with a complete and thorough rebuke of the public health establishment and the Biden administration’s disastrous efforts to censor those who disagreed.
“Public health officials often mislead the American people through conflicting messaging, knee-jerk reactions, and a lack of transparency. Most egregiously, the federal government demonized alternative treatments and disfavored narratives, such as the lab-leak theory, in a shameful effort to coerce and control the American people’s health decisions.
When those efforts failed, the Biden Administration resorted to ‘outright censorship—coercing and colluding with the world’s largest social media companies to censor all COVID-19-related dissent.’”
About time these truths are acknowledged in a public, authoritative manner. Masks don’t work. Lockdowns don’t work. Fauci lied and helped cover up damning evidence.
If only this website had been available years ago.
Though, of course, knowing the media’s political beliefs, they’d have ignored it then, too.
Republished from the author’s Substack
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