New Evidence: Fauci Imposed a Vaccine Delay that Cost Trump the Election
By Toby Rogers | July 31, 2022
I. Fauci fires Trump
Think back to July 2020. Trump and Fauci were at war with each other. Key leaders within the Trump administration, including Peter Navarro, wanted to fire Fauci. There were riots in the streets as people protested the murder of George Floyd. And new evidence shows that behind the scenes, Fauci was working to torpedo Trump’s chances for re-election.
We already knew that Fauci, the FDA, CDC, and the pharmaceutical industry went to great lengths to block safe and effective treatments including hydroxychloroquine and ivermectin in order to prolong the pandemic and create the market for Covid-19 vaccines. But a new book reveals that Fauci also forced Moderna to delay their clinical trial by three weeks — which pushed the release of their preliminary results until after the presidential election.
This key piece of information comes from The Messenger: Moderna, the Vaccine, and the Business Gamble That Changed the World published last week by Harvard Business Review Press. The author, Peter Loftus, is a reporter for the Wall Street Journal and they published his essay about the book in their Review section on Saturday. What’s astonishing is that Loftus does not even realize the enormity of the story he just stumbled upon. Cultural capture and too many shots apparently prevent one from connecting the dots, so I will do it for him.
Most people already know the broad brush strokes of the Moderna story — they had never successfully brought a product to market before Operation Warp Speed. They were grifters — they took $25 million from the Defense Advanced Research Projects Agency (DARPA) in 2013 to develop mRNA products that never worked and another $125 million from the Biomedical Advanced Research and Development Authority (BARDA) in 2015 for a vaccine for Zika that also failed. But Fauci really liked these grifters and so when the pandemic began in 2020, BARDA directed $483 million to Moderna for Covid-19 vaccine development — and Moderna cut NIH in on the patents. That gave NIH and especially Fauci control over what came next.
The key paragraphs from Loftus’ WSJ essay are here:
Dr. Zaks [Chief Medical Officer for Moderna] had wanted to use a private contract research organization to run the whole trial, but NIAID officials wanted their clinical-trial network involved. Eventually, Dr. Zaks backed off, and both entities participated. “I realized we were at an impasse, and I was the embodiment of the impasse,” Dr. Zaks said.
Next, when Moderna’s 30,000-person study began enrolling volunteers in July 2020, the subjects weren’t racially diverse enough. Moncef Slaoui, who led Warp Speed’s vaccine efforts, and Dr. Fauci began holding Saturday Zoom calls with Mr. Bancel and other Moderna leaders to “help coax and advise Moderna how to get the percentage of minorities up to a reasonable level,” Dr. Fauci recalled.
Drs. Fauci and Slaoui wanted Moderna to slow down overall enrollment, to give time to find more people of color. Moderna executives resisted at first. “That was very tense,” Dr. Slaoui said. “Voices went up, and emotions were very high.” Moderna ultimately agreed, and the effort worked, but it cost the trial about an extra three weeks. Later, Mr. Bancel called the decision to slow enrollment “one of the hardest decisions I made this year.”
The claim that Fauci cared about racial diversity in the clinical trial is a lie. How do we know this? Later “clinical trials” for Pfizer and Moderna in kids looked at antibodies in the blood, not actual health outcomes, in only about 300 study participants. The number of people of color enrolled in those undersized trials were in the single digits (literally two or three Black participants total) — so those results were not statistically significant. Yet this did not stop authorization. It appears that Fauci’s delay tactics were designed to accomplish a different goal.
Let’s do the math:
Moderna released their preliminary results — claiming 94.5% effectiveness — on November 16, 2020.
The presidential election was less than two weeks earlier — on November 3, 2020.
Trump lost by less than 1% of the vote in 4 key swing states.
Fauci’s demand to slow down enrollment in July 2020 cost Moderna 3 weeks.
If Moderna had released their results 3 weeks earlier — on October 25, 2020, Trump would have scored a major win in the final week of the campaign and won the election.
It does not matter how one feels about Trump or Biden. A massive political win in the week before the election would have convinced enough voters of Trump’s competence and thus pushed Trump’s vote total over the top.
What about Pfizer? They also could have published their preliminary results prior to the election which would have secured Trump’s re-election. According to Loftus, Pfizer “opted out of Operation Warp Speed for fear it would slow the company down.” Pfizer still took $2 billion off of the Trump administration for advance purchase orders. But Scott Gottlieb and Pfizer clearly preferred Biden and so they held their preliminary results until November 9, 2020 — just 6 days after the election. The Biden administration returned the favor by giving Pfizer a blank check and authorizing shots for additional age groups based on the worst “clinical trial” results anyone has ever seen.
The important thing to understand in all of this is that Fauci, the FDA, NIH, and CDC are political functionaries pretending to be scientists. Pandemics, vaccines, and public health are a way for the Democratic Party machine to direct billions of dollars to their base and reward large donors to the party. These companies and their bureaucratic enablers were happy to take money off of Trump. But they knew that they could get an even better deal from Biden.
As you know, the results of this criminal scheme are gruesome. The Covid-19 shots authorized right after the 2020 election have made no discernible impact on the course of the pandemic. Far more people have died of Covid-19 since the introduction of the shots under Biden than during the Trump administration when no Covid-19 shots existed. The Covid-19 shots have negative efficacy and even quadruple-dosed Biden and quadruple-dosed Fauci have contracted Covid-19, twice. These are the deadliest and most toxic shots in the history of the world.
So what started out as a grift turned into mass murder and a crime against humanity.
And now it’s happening again…
II. Pfizer and Moderna move up the release date for reformulated Covid-19 shots in the effort to help Democrats win the midterm elections
On Thursday of last week, the White House and the FDA told their favorite stenographers at the NY Times that Moderna and Pfizer are going to release their reformulated Covid-19 shots, that will completely skip clinical trials, in mid-September.
As readers of my Substack will recall, back on June 28, Pfizer said that the fastest the reformulated shots could be released was October; Moderna said “late October or November” — provided they could skip clinical trials (which of course the FDA granted because they work for Pharma). Did Pfizer and Moderna not understand their own production capabilities? How did Pfizer and Moderna suddenly speed up their production schedule by 6 weeks?
It appears that once again, the public health gatekeepers are doing politics not science. If shots go into bodies in the last two weeks of September, Democrats will claim progress against Covid during October right before the midterm elections on November 8. It’s basically the political win that these same actors denied to Trump (it’s not a public health win, as I will show below).
What’s likely driving this is that Fauci, Pfizer, Moderna, the FDA, CDC, and NIH all want Democrats to retain the House and Senate in order to prevent hearings into their bungling of the Covid-19 response. Of course they also want to keep the Covid-19 vaccine gravy train going as long as possible.
But, you’re surely saying to yourself, we know that these 5th dose reformulated shots are likely to cause catastrophic harms. We’re already seeing a 5% to 15% increase in all-cause mortality across the most heavily vaccinated countries as a result of non-specific effects from these shots. There are 29,790 VAERS reports of death following these shots and this is likely an underestimate by a factor of 41 (so actual death toll = 1,221,390). These reformulated shots are going to use a form of mRNA never tried before and skip clinical trials altogether, so the harms could be even worse. There also seem to be cumulative harms from these shots — the more doses, the more messed up the immune system, the more vulnerable one is to Covid and all sorts of other diseases including cancer.
So how exactly do they plan to get away with this, especially right before an election?
The same way they always get away with it — they own the media. Pfizer and Moderna will rush out press releases claiming that these reformulated shots are a miracle. The CDC’s in-house newsletter, MMWR, will rush out articles and janky studies claiming that these reformulated shots are a miracle. The mainstream media will dutifully report that these reformulated shots are a miracle. Meanwhile, people you know and love — coworkers, friends, neighbors, and family — will be getting injured and killed by these shots. Yet all of the stories in the news will be hosannas about the genius of Tony Fauci, Peter Marks, and the FDA. Billions of dollars of dark money from Pharma will flow into Democratic Congressional campaign coffers. If Democrats can retain the House and Senate they will reward Pfizer and Moderna by blocking any inquiry into the failed Covid-19 response. Win, win, win for Pharma. Everyone else loses.
Which brings me to my last point….
III. Republicans, you have to step up and fight for us or you will lose
Republicans thought that they could take back the House and Senate simply by not being Democrats. Most Republicans did not really fight for us, they just sat back and let Dems destroy themselves. That plan was working until the Supreme Court overturned Roe. Now the Republican advantage in the generic Congressional ballot (‘which party do you prefer’) has evaporated. Pelosi has passed a range of popular bills. Manchin has fallen in line so Biden will likely get some late legislative wins. Gas prices have declined somewhat. And now it appears that Democrats, who were left for dead just weeks ago, will retain the Senate and may retain the House.
IF REPUBLICANS WANT TO WIN THE MIDTERM ELECTIONS THEY HAVE TO MAKE IT ABOUT DEMOCRATS’ FAILED RESPONSE TO COVID!
No more sitting back. No more making warrior mamas do all of the emotional labor for our country. If Republicans want to win they have to make it clear that they will fire, arrest, and prosecute Fauci (and all of his lieutenants) as soon at Republicans take power. Fauci funded the creation of the chimera virus, blocked access to safe and effective treatments, and inflicted deadly toxic vaccines on the entire population. Over 2 million Americans are dead as a direct result of Fauci’s corruption (1 million dead from/with Covid, over 1 million dead from the shots). If Republicans cannot be bothered to sink this two-foot putt then they don’t deserve to win. If Republicans want the votes of the 18 million single-issue medical freedom voters who decide every national election these days — that’s what they have to run on: #ArrestFauci!
“I’ve Delivered”: New Disclosures Demolish President Biden’s Denials on Hunter Dealings
By Jonathan Turley | July 28, 2022
New disclosures are demolishing the continued denials of President Biden that he had no knowledge and nothing to do with his son’s business interests. The emails (reviewed by Fox and The Daily Mail ) include exchanges with at least 14 of Hunter Biden’s business associates while Joe Biden was vice president. They cast further doubt on the president’s repeated claims that he had no knowledge of his son’s foreign business dealings. In one almost plaintive email, Hunter actually complains to an associate that he had delivered on everything that was demanded of him in getting access to his father and the White House.
President Biden and the White House continue to repeat his denial from the campaign trial in 2019: “I have never spoken to my son about his overseas business dealings.” These denials have continued even after an audiotape surfaced showing President Biden leaving a message for Hunter specifically discussing coverage of those dealings.
Some of us have written for two years that Biden’s denial of knowledge is patently false. Indeed, it is baffling how Attorney General Garland can ignore the myriad of references to Joe Biden in refusing to appoint a special counsel.
There are emails of Ukrainian and other foreign clients thanking Hunter Biden for arranging meetings with his father. There are photos from dinners and meetings that tie President Biden to these figures, including a 2015 dinner with a group of Hunter Biden’s Russian and Kazakh clients.
People apparently were told to avoid directly referring to President Biden. In one email, Tony Bobulinski, then a business partner of Hunter’s, was instructed by Biden associate James Gilliar not to speak of the former veep’s connection to any transactions: “Don’t mention Joe being involved, it’s only when u [sic] are face to face, I know u [sic] know that but they are paranoid.”
Instead, the emails apparently refer to President Biden with code names such as “Celtic” or “the big guy.” In one, “the big guy” is discussed as possibly receiving a 10 percent cut on a deal with a Chinese energy firm; other emails reportedly refer to Hunter Biden paying portions of his father’s expenses and taxes.
The new disclosures only add details to the the extent of his knowledge and involvement. It appears that Biden met with at least 14 of Hunter’s business associates from the U.S., Mexico, Ukraine, China and Kazakhstan over the course of his vice presidency. That includes Hunter’s Mexican business associates, Miguel Aleman Velasco and Miguel Aleman Magnani who visited the West Wing on Feb. 26, 2014, and Joe was later photographed with Hunter giving Velasco and Magnani a tour of the White House Brady Press Briefing room.
Hunter is clearly eager to get photos as a deliverable for the visits. In one email in April 2014 to David Lienemann, Biden’s official photographer, Hunter asks “Do you have pictures from the lunch I had in dad’s office (I think on 2/26) with Miguel Alleman [sic] Sr. And Jr. And Jeff Cooper? If so let me know and I can send someone to pick them up. Thanks. How was Kiev?”
Other emails show Hunter using trips with his Dad to arrange meetings with business associates like Magnani. Indeed, in one exchange with Magnani, Hunter complains that he is not getting responses on his business dealings, objecting
“I have brought every single person you have ever asked me to bring to the F’ing White House and the Vice President’s house and the inauguration and then you go completely silent,. I don’t know what it is that I did but I’d like to know why I’ve delivered on every single thing you’ve ever asked – and you make me feel like I’ve done something to offend you.”
The cringeworthy email only adds to the embarrassment not of Hunter Biden but Merrick Garland who continues to refuse the obvious need for a special counsel. Indeed, the public could raise the objection raised by Hunter: what does it take?
TUCKER CARLSON ON OPIOIDS, COVID AND ANTIDEPRESSANTS
TUCKER CARLSON TONIGHT | JULY 25, 2022
Tucker Carlson reveals the shocking side effects of antidepressants and calls out Democrats for not holding Big Pharma accountable. His full opinion piece can be read here: https://www.foxnews.com/opinion/tucker-carlson-drugs-not-answer-every-human-problem
Google “disinformation” and “election integrity” expert joins The White House
By Christina Maas | Reclaim The Net | July 26, 2022
The long-since established “revolving door” scheme between the White House and Big Tech has continued with the appointment of former Google executive Camille Stewart Gloster as Deputy National Cyber Director with the Office of the National Cyber Director.
And before she joined Google, Gloster was already once working for the government – as a policy adviser in the Department of Homeland Security during the Obama administration.
The White House Office of the National Cyber Director has been operating for a year now, with Gloster slated to deal with workforce programs and security issues pertaining to supply chain; reports say that she will be joining other deputies in the Office who come from Microsoft, the CIA, and the National Security Council.
The practice of giving government jobs to former Big Tech execs, and of Big Tech employing former government officials is frowned upon as one way to establish an infrastructure of what critics fear can – and does – easily turn into “systemic collusion.”
Gloster, meanwhile, is known for her focus at Google, combating what the tech behemoth defines as misinformation on the Android platform – specifically, to “reduce the risk of user harm from misinformation.”
“She joins ONCD from Google, where she most recently served as Global Head of Product Security Strategy, and before that as Head of Security Policy and Election Integrity for Google Play and Android,” the announcement states.
Gloster has praised US and Chinese social media giants, favoring Twitter’s testing of “a community-based points system” to combat “misinformation” – a social credit style fact-checking system for politicians and public figures.
She also welcomed TikTok announcing new rules banning “harmful misinformation,” noting that it was good the super-popular video platform was aware that content posted there can influence political discourse.
Another way to influence political discourse, of course, is to arbitrarily declare content as misinformation and ban or downrank it, a method Big Tech has been employing in earnest over the past years.
Hunter Biden Evidence Wrongly Labeled Disinformation by FBI: Whistleblower

By Oleg Burunov | Samizdat | July 26, 2022
While Hunter Biden was initially probed for his financial and business dealings in foreign countries during his father’s vice presidency, US prosecutors then significantly widened their scope to include Joe Biden’s son’s business associates, their related deals, and the purchase of at least one firearm.
Republican Senator Chuck Grassley has demanded that the Federal Bureau of Investigation (FBI) and the Department of Justice (DoJ) answer a DoJ whistleblower’s allegations that the FBI downplayed damning information about Hunter Biden ahead of the 2020 presidential election.
Grassley is the ranking member on the Senate Judiciary Committee, which oversees the FBI and the DoJ.
In letters to FBI Director Christopher Wray and Attorney General Merrick Garland, the senator revealed that a “highly credible” whistleblower had come forward alleging a widespread effort by some FBI officials to turn a blind eye to negative evidence on President Joe Biden’s son.
“The information provided to my office involves concerns about the FBI’s receipt and use of derogatory information relating to Hunter Biden, and the FBI’s false portrayal of acquired evidence as disinformation,” the letter, in particular, reads.
Grassley insisted that in October 2020, one month before the US presidential election, “an avenue of derogatory Hunter Biden reporting was ordered closed” by a senior FBI agent at the bureau’s Washington Field office.
The senator argued that the allegations obtained by his office “appear to indicate that there was a scheme in place among certain FBI officials to undermine derogatory information connected to Hunter Biden by falsely suggesting it was disinformation.”
According to the Senate Judiciary Committee member, “the volume and consistency of these allegations substantiate their credibility and necessitate this letter.”
DoJ’s Hunter Biden Probe Reportedly Reaches Critical Stage
His letter comes after CNN cited unnamed sources as saying last week that the federal probe into Hunter Biden had reached a “critical juncture” and investigators are weighing whether to charge the president’s son.
The sources told the broadcaster that prosecutors are now primarily focused on tax- and gun-related charges against POTUS’ son.
The firearm charge relates to at least one false statement made by Hunter in his procurement of a weapon. It is believed Biden’s son should have been prohibited from purchasing a firearm due to his self-professed struggles with drug addiction.
In recent months, prosecutors have discussed the matter with DoJ officials and investigators from both the FBI and Internal Revenue Service (IRS), according to the insiders.
The DoJ’s probe specifically looks into the contents of Hunter Biden’s so-called “laptop from Hell”, including compromising emails, naked photos and graphic videos that have been released since 2020, when the New York Post was the first to make public several emails from the device.
The laptop uncovered details about unseemly and potentially illegal activities by the president’s son, ranging from crack cocaine and alcohol-fueled parties with high-priced prostitutes to “business deals” involving the trading of cash for access to the elder Biden during his tenure as Barack Obama’s vice president.
Joe Biden has repeatedly dismissed any knowledge of his son’s business activities, and most news outlets and social media companies successfully shielded him from the laptop’s revelations ahead of the 2020 presidential election campaign, at which time the computer was dismissed as a “Russian disinformation operation.”
Earlier this year, the New York Times and The Washington Post changed course, confirming that the laptop was authentic and that the damning information contained within was real.
Washington is the problem, not the solution, so why is Abbas seeking new ‘powerful’ sponsors?
By Ramzy Baroud | MEMO | July 25, 2022
To describe US President Joe Biden’s recent visit to Israel and Palestine as a “failure” in terms of activating the dormant “peace process” is to use a misnomer. For this statement to be accurate, Washington would have had to indicate that it had even a nominal desire to push for negotiations between the Israeli government and the Palestinian leadership.
Political and diplomatic platitudes aside, the current US administration has done the exact opposite, as indicated by Biden’s words and actions. Alleging that the US commitment to a two-state solution “has not changed”, Biden dismissed his administration’s interest in trying to achieve such a goal by declaring that the “ground is not ripe” for negotiations.
Given that the Palestinian Authority led by Mahmoud Abbas has repeatedly announced its readiness to return to negotiations, one can only assume that the process is being stalled due to Israel’s intransigence. Indeed, none of Israel’s top leaders or major parties champion negotiations — the so-called peace process — as a strategic objective.
However, Israel is not the only one to blame. The Americans have also made it clear that they have moved on from that political sham altogether, one which they invented and then sustained for decades. In fact, the final nail in the “negotiated solution” coffin was hammered in by the Donald Trump administration, which has simply backed every Israeli claim and shunned all legitimate Palestinian demands.
The Biden administration has been blamed habitually by Palestinians, Arabs and progressive voices within the Democratic Party for failing to reverse Trump’s prejudiced moves in favour of Israel: moving the US Embassy from Tel Aviv to Jerusalem, for example; shutting down the US Consulate in East Jerusalem; and accepting the unfounded Israeli claims regarding its jurisdiction over illegal Jewish settlements built on occupied Palestinian land. The list goes on.
Even if one assumes that the Biden administration is capable of reversing some or all of Trump’s unlawful actions, what good would that be in the greater scheme of things? Washington was, and remains, Israel’s greatest benefactor, funding its military occupation of Palestine with an annual gift of $4 billion, in addition to many other schemes, including a massive and growing budget allocated just for Israel’s Iron Dome missile defence system.
As horrific as Trump’s years were in terms of undermining a just resolution to the Israeli occupation of Palestine, Biden’s policies are but a continuation of an existing pro-Israel American legacy that surpasses that of Trump by decades.
For Israel, the “peace process” has served its purpose, which explains the infamous declaration by the CEO of the Jewish settlement council, Yesha, in the occupied West Bank in 2018: “I don’t want to brag that we’ve won… Others would say it appears that we’re winning.”
However, Israel’s supposed “victory” following three decades of a fraudulent “peace process” cannot be credited to Trump alone. Biden and other top US officials have also been quite useful. While it is understood widely that US politicians support Israel out of self-interest — they need, for example, to appease the influential pro-Israel lobby in Washington — Biden’s support for Israel has an ideological foundation. The US president was less than bashful when he repeated his famous statement at Israel’s Ben Gurion airport on 13 July: “You need not be a Jew to be Zionist.”
Consequently, it may appear puzzling to hear Palestinian officials call on the US — and Biden specifically — to put pressure on Tel Aviv to end its 55-year occupation of East Jerusalem, the West Bank and Gaza Strip.
Mohannad Al-Aklouk, the Palestinian representative at the Arab League, is just one who has repeated the same clichéd and unrealistic language of expecting the US to “exert practical pressure on Israel”, “set the stage for a fair political process based on international law”, and “meet its role as a fair sponsor of the peace process”. Strangely, Al-Aklouk truly believes that Washington, with its dismal track record of pro-Israel bias, can be the saviour of the Palestinians.
Another Palestinian official told the New Arab that PA President Abbas was “disappointed with the results of Biden’s visit” as, apparently, the Palestinian leader “expected that the US president would make progress in the peace process.” The same source added that Abbas’s authority is holding meetings with representatives from “powerful countries” to replace the US as sponsors of the negotiations.
Abbas’s political stance is confusing. The “peace process” is, after all, an American invention. It was a unique, self-serving style of diplomacy that was formulated to ensure Israel’s priorities remain centre stage of US foreign policy in the Middle East. In the Palestinian case, the “peace process” served only to entrench Israel’s colonisation of Palestine, while degrading, or completely sidelining, legitimate Palestinian demands. This “process” was also constructed with the aim of marginalising international law as a political and legal frame of reference for the Israeli occupation of Palestine.
Instead of questioning the entire “peace process” apparatus and apologising for the strategic blunder of pursuing American mirages at the expense of Palestinian rights, the Palestinian Authority is still clutching desperately to the same old fantasy, even when the US and Israel have long abandoned the political farce that they created.
Even if China, Russia or India, for example, would agree to be the new sponsors of the “peace process”, there is no reason for Tel Aviv to engage in future negotiations when it is able to achieve its colonial objectives with full support from the US. Moreover, none of these countries have, for now, much leverage over Israel, and so are unable to sustain any kind of meaningful pressure on Tel Aviv to respect international law.
Yet, the PA is still holding on, simply because the “peace process” has proved to be greatly beneficial in terms of funds, power and prestige enjoyed by a small but powerful class of Palestinians that was formulated largely after the Oslo Accords in 1993.
It is time for Palestinians to stop investing their political capital in the Biden or any other administration. What they need is not a new “powerful” sponsor of the “peace process”, but a grassroots-based struggle for freedom and liberation starting at home, one that galvanises the energies of the Palestinian people themselves. Alas, this new paradigm cannot be achieved when the priorities of the Palestinian leadership remain fixated on the financial handouts and political validation of Washington and its Western allies.
Biden Is Extending The Covid Emergency And Prolonging The War On Doctors
By Pierre Kory, MD | The Federalist | July 22, 2022
A recent New York Times/Siena College poll showing 64 percent of Democrats preferring a new standard-bearer in 2024 rocked the White House and the political landscape, but it should not have come as a big surprise. After all, President Joe Biden continues to fall short of the promises that drew many Democrats, including myself, to his candidacy in 2020: his pledge for a new strategy combatting Covid-19.
Consider the Food and Drug Administration’s recent decision allowing pharmacists to play doctor and prescribe Pfizer’s anti-viral treatment Paxlovid, which Biden himself, having contracted Covid-19, is now taking. The agency claims this is meant to increase access to the medicine, which must be taken as soon as symptoms arise. But the drug’s fact sheet is a tangled web of restrictions that will make it impractical for most pharmacies to take the risk. Why is the FDA encouraging this?
The answer is plain to anyone who has been following the plight of independent doctors during the pandemic. Our public health agencies — heavily influenced by the pharmaceutical industry and beholden to Biden’s “vaccine first” approach — are committed to diminishing the medical profession and centralizing authority with bureaucrats in Washington, D.C. They have prosecuted a relentless campaign to reduce physicians to cogs in a health care system that is aggressively transforming all medical professionals from providers to prescribers.
The problems with Paxlovid are no secret. FDA granted Pfizer emergency use authorization for the drug after a single trial with questionable results. The medicine has many contraindications, meaning it can’t be taken by someone who simultaneously would be taking certain anti-depressants, anti-seizure, anti-psychotic, cholesterol, or blood pressure medications. Furthermore, many Americans cannot take Paxlovid, given that nearly half of adults have cardiovascular disease.
The risks are plain to see in FDA’s guidance, which recommends referring the patient to a doctor if “sufficient information is not available to assess renal and hepatic function” or “potential drug interactions.” Numerous contraindications are listed, and caution is advised throughout. The burden is on the patient to furnish medical records to prove that he or she doesn’t have any significant kidney or liver disease, drug sensitivities, or other medications that could cause serious adverse events.
Nevertheless, pharmacies have spent months and millions of dollars lobbying for the right to play doctor and prescribe Paxlovid. The economic motives of such a move are clearly in their favor, as, unlike doctors, they profit directly from dispensing drugs. It’s no surprise the National Community Pharmacists Association celebrated the win as a “course correction.” Its CEO said, “Pharmacists are the drug therapy and drug interaction experts. This move opening up their ability to assess the need for and prescribe Paxlovid will improve patients’ timely access to treatments that will help keep them out of the hospital and alive.”
This may be as absurd a statement by a health organization as any I have heard in the pandemic. No pharmacist could ever safely dispense a novel medicine with an unprecedented amount of drug interactions without in-depth knowledge of the severity of the patient’s medical problems or the critical necessity of each of their other medicines. This fact was not lost on the American Medical Association, which temporarily snapped out of its woke-activist-induced coma to offer qualified criticism.
“While the majority of COVID-19 positive patients will benefit from Paxlovid, it is not for everyone, and prescribing it requires knowledge of a patient’s medical history, as well as clinical monitoring for side effects and follow-up care to determine whether a patient is improving—requirements far beyond a pharmacist’s scope and training,” American Medical Association President Jack Resneck Jr. said in a statement.
The tell is right there, though. The AMA is fine with Paxlovid as long as physicians are doing the prescribing. Ceding authority is the problem, which is why the agency previously called the idea “dangerous in practice and precedent” when the Biden administration first proposed it in the Test to Treat initiative.
Covid cases and deaths are down massively from their last peak in January. Most states have lifted restrictions and returned to normal. Yet just days after the FDA made this announcement, the Biden administration again extended the Covid public health emergency — because the president can’t lose the specter of Covid as a political tool.
Vaccination rates have leveled off, and Paxlovid sales bottomed out in April due to a combination of supply problems and sinking demand. Pfizer pushed expectations for the drug sky high, and now it needs to deliver on that promise. The FDA’s move shows how deftly the company has used the pandemic to influence government and public health agencies to serve its shareholders.
The pharmaceutical industry, led by Pfizer and in league with the Biden administration, is waging war against independent doctors who refuse to cede control over patient well-being — and they are winning. If there is any hope for change, it will come in November.
The red wave forming off our political shores is a culmination of many factors. Inflation and gas prices are hitting all-time highs, and just 13 percent of Americans believe the country is heading in the right direction. But relying on scare tactics to distract voters back to Biden is a strategy not supported by medical conditions on the ground.
Let’s hope whoever rides into Washington on that red wave will take on this fight with integrity.
Pierre Kory, MD, is president and chief medical officer of the Front-Line COVID-19 Critical Care Alliance.
Ukraine’s Naftogaz Reportedly Requests $5Bln in Government Subsidies to Buy Gas Ahead of Winter
Samizdat – 20.07.2022
Ukraine’s state-run oil and gas company Naftogaz has requested 150 billion Ukrainian hryvnias ($5 billion) in subsidies from the government to purchase enough gas ahead of the heating season, the RBC Ukraine news agency reported on Wednesday, citing the firm’s letter to the government.
Naftogaz had to request budgetary help since raising such massive funds otherwise is neither possible domestically nor internationally, the company wrote in the letter to the cabinet, according to the report.
“In such conditions, the state budget is the only possible source of financing the purchase of imported natural gas… The most favorable option is to increase the authorized capital of Naftogaz of Ukraine,” the letter read, according to the report.
The company suggested increasing its authorized share capital by 150 billion Ukrainian hryvnias, the report said.
On July 12, Naftogaz asked the holders of its Eurobonds to defer interest payments for two years but was not granted such concession, thereby exposing the company to the risk of default.
Ukraine’s former housing and communal services minister, Oleksiy Kucherenko, has accused Naftogaz of forging its profit results in 2021, saying that the breach now has to be patched with 264 billion hryvnias from the budget. The ex-official also noted that Ukraine’s budget is running low, so Kiev may have to request assistance from the United States.
How Pfizer Profited From the Pandemic
By Dr. Joseph Mercola | July 18, 2022
According to Kaiser Health News (KHN),1 the COVID-19 pandemic has been a real boon to Pfizer. Not only has it yielded “outsize benefits” in terms of profits, but it has also “given the drugmaker unusual weight in determining U.S. health policy.”
“Based on internal research, the company’s executives have frequently announced the next stage in the fight against the pandemic before government officials have had time to study the issue, annoying many experts in the medical field and leaving some patients unsure whom to trust,” KHN reporter Arthur Allen writes, adding:2
“When last year Bourla suggested that a booster shot would soon be needed, U.S. public health officials later followed, giving the impression that Pfizer was calling the tune.
Some public health experts and scientists worry these decisions were hasty, noting, for example, that although boosters with the mRNA shots produced by Moderna and Pfizer-BioNTech improve antibody protection initially, it generally doesn’t last.
Since January, Bourla has been saying that U.S. adults will probably all need annual booster shots, and senior FDA officials have indicated since April that they agree … The company’s power worries some vaccinologists, who see its growing influence in a realm of medical decision-making traditionally led by independent experts …
When President Biden in September 2021 offered boosters to Americans — not long after [Pfizer CEO Albert] Bourla had recommended them — Dr. Paul Offit, director of the Vaccine Education Center at Children’s Hospital of Philadelphia … wondered, ‘Where’s the evidence you are at risk of serious disease when confronted with COVID if you are vaccinated and under 50?’
Policies on booster recommendations for different groups are complex and shifting, Offit said, but the CDC, rather than Bourla and Pfizer, should be making them. ‘We’re being pushed along,’ he said. ‘The pharmaceutical companies are acting like public health agencies.’”
The fact that a vaccine-pusher like Offit — infamous for claiming a baby can safely tolerate 10,000 vaccines at once3 — is questioning and pushing back against Pfizer’s influence over health policy reveals just how brazen, unethical and potentially dangerous that is.
Massive Profits Made From Useless Products
According to Allen, Pfizer’s revenue in 2021 was $81.3 billion4 — approximately double that of 2020 — and the COVID shot accounted for $36.78 billion5 of that. For comparison, Lipitor, Pfizer’s previous top selling statin, generates roughly $2 billion a year,6 while their strep vaccine, Prevnar 13 rakes in $6 billion a year.7
Its mRNA gene transfer injection against COVID now dominates 70% of the U.S. and European markets, and Paxlovid, Pfizer’s COVID drug, has become a standard treatment choice in hospitals. This, despite researchers finding Paxlovid (molnupiravir) causes severe rebound and supercharges mutations.
In a rational scenario, that finding would have put a stop to its use, but no. In an official health advisory8 to the public, issued May 24, 2022, the U.S. Centers for Disease Control and Prevention first warns that Paxlovid is associated with “recurrence of COVID-19 or ‘COVID-19 rebound,’” and then in the very next sentence stresses in bold print a narrative supporting its use and enriching Pfizer with instructions saying:
“Paxlovid continues to be recommended for early- stage treatment of mild to moderate COVID-19 among persons at high risk for progression to severe disease.”
Allen also notes that, during an investor call, a Pfizer official highlighted reports of Paxlovid’s failure, but spun it into “good news” for investors, as patients may require multiple courses!9 Obviously the objective has long ago shifted from helping humans to raping them for as much profit as possible.
Similarly, while Pfizer’s COVID jab clearly doesn’t prevent infection or spread, and Americans are rejecting the shots in growing numbers — 82.2 million doses had expired and were chucked in the trash as of mid-May 202210 — the U.S. government still went ahead and ordered another 105 million doses at the end of June 2022.
These are intended for a fall booster campaign, at a cost to taxpayers of $3.2 billion.11 The U.S. is actually paying about 50% more for each of these new jab boosters this time around — $30.47 per dose compared to $19.50 per dose paid for the first 100 million doses.
The U.S. government has also promised to purchase another 20 million courses of Paxlovid, at an eye-watering cost of $530 per five-day course. Basically, Pfizer is being financially rewarded for producing products that are useless at best and dangerous at worst, and we’re all paying for it. In case you’re curious, that is another $10.6 billion transferred from U.S. taxpayers to Pfizer.
Future Boosters Won’t Undergo Human Clinical Trials
After you likely thought it couldn’t ever get any worse, KHN also touches on, but doesn’t delve into, the fact that Pfizer suggested they skip human trials as they move forward with jabs that are reformulated for newer variants. If this strikes you as crazy, you’d be right. It’s sheer madness, but the U.S. Food and Drug Administration — a clearly captured agency — has already surreptitiously agreed to this egregious miscarriage of science.
How this wicked scheme, known as the “Future Framework,”12 was adopted by the FDA without formal vote is explained by Toby Rogers, Ph.D. — a political economist whose research focus is on regulatory capture and Big Pharma corruption13 — in the video above. He also explained it in a June 29, 2022, Substack article:14
“Yesterday [June 28], the FDA’s Vaccines and Related Biological Products Advisory Committee approved a bivalent COVID-19 shot with the Wuhan strain and the Omicron variant … Wait, hold up, I thought the FDA was voting on the Future Framework yesterday?
The policy question was whether reformulated COVID-19 shots would be treated as new molecular entities (which they are) in which case they should be subject to formal review or whether reformulated shots would be treated as ‘biologically similar’ to existing Covid-19 shots and be allowed to skip clinical trials altogether.
Apparently the FDA did not have the votes to just pass this as a policy question. If you ask anyone whether reformulated mRNA represents a new molecular entity, well of course it is, so that would require formal regulatory review.
What the FDA did instead was to smuggle the policy question in disguised as a vote about reformulated ‘boosters’ for the fall.
In essence, the FDA just started doing the Future Framework (picking variants willy nilly, skipping clinical trials) and essentially dared the committee members to turn down a booster dose — knowing that all of the VRBPAC members are hand-picked because they’ve never met a vaccine they did not like.
So of course only two people on the committee had the courage to turn down a booster dose — even though it was based on this preposterous process (that was never formally adopted) where there was literally no data at all … By stealth, the FDA replaced a system based on evidence with a system based entirely on belief.”
Countries Held to Ransom
In 2021, secret details of Pfizer’s contracts came to light, showing they are essentially holding countries hostage to nonnegotiable demands for payment in full AND freedom from liability.15
In late February 2021, The Bureau of Investigative Journalism reported16 that Pfizer was demanding countries put up sovereign assets as collateral for expected vaccine injury lawsuits resulting from its COVID-19 jab.
Several countries, including Brazil, Chile, Colombia, the Dominican Republic and Peru, agreed to this demand, putting up bank reserves, military bases and embassy buildings as collateral. In short, theses governments are guaranteeing Pfizer will be compensated for any expenses resulting from injury lawsuits against it, so the company won’t lose a dime if its COVID shot injures people.
Shockingly, these terms are binding even if those injuries are the result of negligent company practices, fraud or malice!
In October that same year, Public Citizen published the secret contracts17,18 between Pfizer and Albania, Brazil, Colombia, Chile, Dominican Republic, the European Commission, Peru, the U.S. and the U.K., further revealing the extent to which these countries handed power over to Pfizer. In almost all scenarios, Pfizer’s interests come first.
For example, government purchasers must acknowledge that the effectiveness and safety of the shots are completely unknown, all while indemnifying Pfizer against any and all financial liability. This is the ultimate corporate maleficence, using their leverage to force the kill shot down these countries’ throats and avoiding any personal responsibility for damages.
Even if Pfizer eventually is convicted of fraud in the U.S. and loses all its liability protection from the COVID jabs because of it, that judgment would not impact these foreign contracts. These countries sold their souls to Pfizer and have absolutely no recourse but to pay even if the shots kill everyone.
The contracts for at least four countries also secure Pfizer’s intellectual property rights even if the company is found to have stolen intellectual property rights of others. In such case, the government purchaser becomes the liable party. As explained by Public Citizen :19
“For example, if another vaccine maker sued Pfizer for patent infringement in Colombia, the contract requires the Colombian government to foot the bill. Pfizer also explicitly says that it does not guarantee that its product does not violate third-party IP, or that it needs additional licenses.
Pfizer takes no responsibility in these contracts for its potential infringement of intellectual property. In a sense, Pfizer has secured an IP waiver for itself. But internationally, Pfizer is fighting similar efforts to waive IP barriers for all manufacturers.”
Equally shocking is that countries are forced to follow through on their vaccine orders even if other drugs or treatments emerge that can prevent, treat or cure COVID-19.20 Is it any wonder, then, that governments around the world have suppressed the use of safe and effective outpatient drugs like hydroxychloroquine and ivermectin?
If these drugs were allowed to be used and could be proven to work, the COVID injections would be completely unnecessary and their emergency use authorization would disappear, yet governments are on the hook for hundreds of millions of doses.
Pfizer Has ‘Habitual Offender’ Track Record
The fact that Pfizer has behaved like a criminal who works out a cover story for a planned murder before committing it is not surprising, considering its history. Pfizer, has been sued in multiple venues over unethical behavior, including unethical drug testing and illegal marketing practices.21
In his 2010 paper,22 “Tough on Crime? Pfizer and the CIHR,” Robert G. Evans, Ph.D., Emeritus Professor at Vancouver School of Economics, described Pfizer as “a ‘habitual offender,’ persistently engaging in illegal and corrupt marketing practices, bribing physicians and suppressing adverse trial results.”
Between 2002 and 2010 alone, Pfizer and its subsidiaries were fined $3 billion in criminal convictions, civil penalties and jury awards. They are recurrent criminal felons. None of these convictions has deterred their nefarious behavior.
In 2011, Pfizer agreed to pay another $14.5 million to settle federal charges of illegal marketing,23 and in 2014 they settled federal charges relating to improper marketing of the kidney transplant drug Rapamune to the tune of $35 million,24 as well as $75 million to settle charges relating to its testing of a new broad spectrum antibiotic on critically ill Nigerian children.
As reported by the Independent 25 at the time, Pfizer sent a team of doctors into Nigeria in the midst of a meningitis epidemic. For two weeks, the team set up right next to a medical station run by Doctors Without Borders and began dispensing the experimental drug, Trovan. Of the 200 children picked, half got the experimental drug and the other half the already licensed antibiotic Rocephin.
Eleven of the children treated by the Pfizer team died, and many others suffered side effects such as brain damage and organ failure. Pfizer denied wrongdoing. According to the company, only five of the children given Trovan died, compared to six who received Rocephin, so their drug was not to blame.
The problem was they never told the parents that their children were being given an experimental drug. What’s more, while Pfizer produced a permission letter from a Nigerian ethics committee, the letter turned out to have been backdated. The ethics committee itself wasn’t set up until a year after the trial had already taken place. Pfizer’s rap sheet also includes bribery, environmental violations, labor and worker safety violations and more.26
Wolves in Sheep’s Clothing
Now, despite Pfizer being one of the least ethical drug companies, we’re told to trust them with our very lives, and the lives of our precious children. They’re going to put out booster shots this fall that have undergone absolutely no testing whatsoever, and we’re to simply throw caution to the wind because Pfizer — which has no liability whatsoever — says so.
In 2014, Pfizer faced a surge of lawsuits that accused it of hiding known side effects of its anticholesterol drug Lipitor.27 They got off scot-free that time, as a federal judge dismissed thousands of cases alleging the drug caused Type 2 diabetes.28,29 But at least they had liability and could be sued.
When it comes to the COVID jabs, injured patients and family members of those killed by it won’t even have the ability to sue for damages, as governments around the world have indemnified them completely, and it looks as though they might not even be liable even if they’re found guilty of fraud. But we will have to see what the courts rule on that one. Still, that any nation would agree to a contract like that is just mindboggling.
Meanwhile, mounting evidence shows the COVID shots destroy immune function over time, and Pfizer’s own trial data reveal deaths and serious adverse events numbering in the tens of thousands.
It’s hard to tell who’s more deserving of punishment — Pfizer or the equally captured federal agencies, the FDA and the CDC, that go along with them and do nothing to protect the lives of the youngest members of our society. Clearly, it’s up to us to protect ourselves and our loved ones, because wolves in sheep’s clothing are ruling the roost — they’re making all the decisions, and captured agencies are simply doing their bidding.
Sources and References
- 1, 2, 4, 9 KHN July 5, 2022
- 3 Science Daily January 10, 2002
- 5 Washington Examiner February 8, 2022
- 6 Axios October 30, 2019
- 7 True Cost of Health Care
- 8 CDC Advisory May 24, 2022
- 10 NBC News June 6, 2022
- 11 Businesswire June 29, 2022
- 12 FDA Briefing Document June 28, 2022
- 13 Brownstone Institute June 22, 2022, Author’s Bio
- 14 uTobian June 29, 2022
- 15 STAT News February 23, 2021
- 16 The Bureau of Investigative Journalism February 23, 2021
- 17, 19 Public Citizen October 19, 2021
- 18 Twitter Zain Rizvi October 19, 2021
- 20 COVID19up.org August 17, 2021 (archived)
- 21 SGT Report January 7, 2021
- 22 Healthcare Policy 2010 May;5(4):16-25
- 23 DOJ October 21, 2011
- 24 Reuters August 6, 2014
- 25 The Independent March 23, 2014
- 26 Corporate Research Project Pfizer
- 27 Reuters August 8, 2014
- 28 Drugwatch Lipitor Lawsuits
- 29 Reuters May 12, 2021
220-Meter Turbine Breaks in Two in One of Sweden’s Largest Wind Parks

Samizdat – 18.07.2022
A 220 meter high wind turbine with a span of 145 meters, part of a wind farm in Viksjö outside the city of Härnösand in Västernorrland County, has broken in half and crashed into the forest.
No one was injured and the wind farm will be closed until an accident team examines the wind farm.
According to the Nysäter Wind company, which owns the farm, no one was injured. An accident team is on its way to investigate the wind turbine, and is expected to begin its work on Monday. Until then, the farm is closed, and access to the adjacent areas is limited.
“Parts of the turbine are sticking up and leaning against each other. That is why we approach with caution and block off. We also ask ourselves the question of how this could happen. We hope that the investigation can find out,” Nysäter Wind board member and advisor Per Nordlund told national broadcaster SVT.
Nysäter Wind suspected that oil had leaked from the gearbox and urged the public to stay away from the site.
The Nysäter windfarm in Viksjö is touted as one of Sweden’s largest wind power projects. With its 114 turbines, it will be one of Europe’s largest onshore wind turbines and by far the largest investment ever in the history of Härnösand.
However, the wind farm in Viksjö previously ran into trouble during the construction stage. Journalist investigations by SVT and others indicated that subcontractors had been left unpaid for their work, which led to bankruptcy risks, and about 30 companies being owed money to the tune of at least SEK 60 million ($5.7 million).
No fewer than six reported violations of environmental regulations were reported during construction; forests with protected species were felled and waste was dumped in sensitive natural environments.
Furthermore, the massive project was stopped by the county administrative board over environmental criticism, leading to further delays in construction. Only in June 2022 was the park ready for inauguration.
The share of domestic wind power resources in Swedish national consumption has risen from 0.3 percent in 2000 to 20.3 percent in 2020.
To counter soaring electricity prices and alleviate Europe’s dependence on energy fuels, the Swedish government plans a massive expansion of offshore wind power. However, critics slammed the plans as inefficient and a way of shifting the bill to the customers themselves. Among others, energy expert Marie Knutsen-Öy called it “an indirect subsidy that creates unnecessary costs and impairs the functioning of the electricity market”.

If you regard the United States as perhaps flawed but overall a force for good in the world . . .