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‘Follow the Science’: Have the Bad Guys Finally Gone Too Far?

By Sharyl Attkisson | The Defender | September 9, 2024

In this exclusive excerpt from her new bestseller, “Follow the Science: How Big Pharma Misleads, Obscures, and Prevails,” journalist Sharyl Attkisson details how public health agencies and some public universities are so captured by commercial interests that they function as little more than an advertising arm of Big Pharma.

In the case of vaccine makers, success comes with inventing shots that can be added to the list of what’s required for schoolchildren. Better yet, invent shots that the public can be convinced to get, repeatedly, for the rest of their lives. Instant billion-dollar blockbuster!

This has led to a questionable dynamic where the one-time standard that vaccines were required to meet — that they must be vital, safe, and effective — fell by the wayside. Instead the government aggressively serves as promoter of dubious versions that may not be necessary, may not work very well, and come with the risk of serious side effects.

In 1975, the cost of vaccinating a child from birth to age six was $10 (in 2001 terms, adjusted for inflation). As more vaccines were added to the list, the cost ballooned to $385 in 2001. Today it’s thousands of dollars. The costs are largely hidden to us since we get inoculated for free or with minimal out-of-pocket payments. But make no mistake, we’re paying the bills in the form of insurance premiums, and tax dollars to state and federal programs that provide vaccines at little to no direct cost to the patient. Vaccine companies are reaping enormous profits.

Sometimes getting and keeping a vaccine on the market requires sleight of hand. The Centers for Disease Control (CDC), our premier infectious disease federal health agency, is happy to give a little help to its vaccine industry partners or, as the CDC calls them, “stakeholders.” The agency’s best and brightest can even adjust the veritable meaning of the word “vaccine.”

The CDC used to define “vaccines” quite simply as agents that “prevent disease.” But in 2021, that had to be changed. It became undeniable that Covid vaccines didn’t prevent the disease (or transmission, or even illness). Logic might suggest that the Covid vaccines would have to be withdrawn from the market. After all, they didn’t even meet the definition of a vaccine. Instead the CDC quietly redefined the word “vaccine” to make the Covid shots seem successful after all.

On the CDC’s vaccine web page, sometime between September 1 and 2, 2021, somebody removed a key phrase from the definition. On September 1, the CDC defined a vaccine as “a product that stimulates a person’s immune system to produce immunity to a specific disease, protecting the person from that disease.” But on September 2, the phrase “protecting the person from that disease” was removed, like it never even happened. Now, the CDC says, vaccines merely “stimulate the body’s immune response.”

Think of it. The CDC unilaterally redefined two hundred years’ of the world’s understanding of what constitutes a vaccine, without so much as an explanation, public discussion, hearing, or vote. Once you understand that our top, trusted medical authorities are willing to sneakily move goalposts and change meanings of words to protect a market, you’re a long way to beginning to understand how deep the corruption goes.

It’s one thing to be barraged by marketing to convince you to buy a shiny new car. But it’s quite another to get sold a bill of goods by our trusted health experts when it comes to our most precious possession. Our increasingly elusive quest for good health has become a commodity to be bought and sold by today’s snake oil salesmen and their coconspirators, but on a far grander scale …

In their defense, pharmaceutical companies are doing exactly what they were built to do: make money. The thought that they’re somehow different from other multinational corporations, that they are motivated by altruism and can be trusted to be honest about the failings of their own products, is a fallacy. There’s no law that requires them to put patient health ahead of profits. There’s nothing that forces them to stop promoting a pill even if they secretly know it doesn’t work or has dire side effects. It could be argued they have a fiduciary duty to try to downplay or even cover up negative information about their products if it could hurt their bottom line.

Our sick and broken system is the fault of politicians, federal agencies, the medical establishment, and the media. They have a far different responsibility than private drug companies. But they’ve allowed themselves to be so captured by commercial interests that they function as little more than an advertising arm of the pharmaceutical industry

It’s grown exceedingly common that when patients get sick during a study, instead of the drug company considering the illness to be a possible side effect — which is what should be the response — they seek to explain it away. They blame anything other than the experimental medicine.

Another blatant example of this twisting of science can be found in a May 2023 study to look at whether serious neurological, or brain and nerve, disorders were connected to Covid-19 vaccines. The study was entitled, “Observational Study of Patients Hospitalized With Neurologic Events After SARS-CoV-2 Vaccination.” It was published in Neurology Clinical Practice.

The first problem I see when reviewing the study is that, although some side effects don’t surface until months or years after a medicine is taken, the study scientists drew their conclusions based on a mere six-week period. They looked at only 138 people hospitalized after a Covid vaccination, and a limited number of neurological conditions, including stroke or blood clots, encephalopathy or brain damage, seizure, and intracranial bleeding.

But what really captures my attention is the study’s nonsensical conclusion. It states that since all 138 vaccinated, hospitalized patients had “risk factors” or “established causes” for their neurologic illnesses, such as high blood pressure for stroke victims, this proves the Covid vaccines are safe. “All cases in this study were determined to have at least 1 risk factor and/or known etiology accounting for their neurologic syndromes. Our comprehensive clinical review of these cases supports the safety of mRNA COVID-19 vaccines,” reads the study discussion.

You don’t have to be a scientist to detect a serious flaw in their reasoning. It’s like claiming that an old person who falls down the stairs and breaks a hip — was injured by being old, and it had nothing to do with the fall down the stairs. Having high blood pressure to begin with doesn’t mean if you have a stroke after Covid vaccine, you can automatically rule out the vaccine as having an impact. In fact, you should immediately ask whether the vaccine might prove riskier to people with preexisting vulnerabilities.

Surely even a novice scientist should know this. So why did this ridiculous study get published? It looks suspiciously as if someone is trying to dispel growing safety concerns about the vaccines. I decide to find out who.

I learn that the study was conducted at Columbia University Irving Medical Center and New York–Presbyterian Hospital in New York City. It was funded by taxpayer money through the CDC. I email the primary study author, Dr. Kiran Thakur: “The study seems to imply that because people who suffered certain neurological events shortly after Covid vaccination had risk factors, it exonerates the vaccines from blame. But did the authors consider that people with existing risk factors could be at greater risk for vaccine adverse events?”

Instead of answering the question, Dr. Thakur replies, “Can you clarify the purpose of your questions (to be published, personal inquiry or otherwise).” When I reply that her responses might be published, she goes dark on me. When I persist in asking her to respond, she finally answers: “Declining, thank you.” Why isn’t a legitimate scientist happy to answer a simple question about her work? What’s the big secret?

Reaching a dead end with Dr. Thakur, I query the medical journal’s editorial staff. They loop me back to Dr. Thakur, saying only she can answer my questions. Shouldn’t the journal be asking the same questions?

Next I turn to Columbia University. I ask to see the study materials and related communications. I want to learn Who was behind this study, and did the peer reviewers or anybody else flag the obvious flaws? It’s a reasonable request because we, the public, funded the research and own the information. Besides, a basic tenet of scientific research dictates that there should be transparency in data and all aspects of studies. In fact, a study isn’t considered legitimate unless the data is available so that it can be verified and replicated by others with the same results.

But Columbia University stalls in responding to my emails. So I file a formal Freedom of Information Act (FOIA) request for the material. More time passes, and Columbia informs me that it’s a private institution and it doesn’t have to follow Freedom of Information Act law. I appeal on the basis of scientific transparency. Why does Columbia want to keep details of an important, publicly funded study secret? Isn’t that contrary to tenets of sound science? My appeal falls on deaf ears. University officials tell me they’ll only respond to validly issued and served subpoenas or court orders, and that “[s]ubpoenas to the University must be served on the Office of the General Counsel.”

Think of the audacity. A private university can take our tax money for a study, then refuse to answer questions about it because they’re a private university. To me it looks like the CDC can legally launder taxpayer dollars to third parties to produce what amounts to propaganda, then cover their tracks under a shroud of secrecy.

Next, I decide to file a FOIA request directly with the CDC, which is undeniably subject to the Freedom of Information Act. However, I know from experience that federal agencies spin the FOIA process into a tool to obfuscate. They rarely follow the provisions requiring them to turn over materials within twenty working days. And punishment for their violations is virtually nonexistent.

Sure enough, the CDC sits on my FOIA request for forty-two days before emailing to let me know they haven’t yet begun processing my request. They say I need to be much more specific, or they won’t consider responding. This raises one of the newer tricks federal agencies use to make it tougher for us to access information we own. They require FOIA requests to be impossibly precise. In the past, it was enough for a requester to provide a topic and date range. Agencies would search computer records using keywords. But now they claim they can’t do that.

The CDC FOIA officers now demand that I somehow discover and present them with names of each specific, archaic department and subdepartment that should be searched and the title of any documents I’m looking for. They further insist I provide names and titles of each person within those departments whose email accounts should be searched. And I must give them the number of the grant that awarded the taxpayer funds for the study. Problem is, I have no way to know any of that. The grant number was strangely omitted from the published study, and I have no clue how I would find names of the people who might have records, or what departments they work in. That’s a key part of what the FOIA response would reveal. Using these avoidance tactics, a federal agency can heighten their odds of keeping public documents secret …

There may be a silver lining. The bad guys finally went too far.

With Covid: the disinformation, intolerance for dissent, shutdowns, mandates, forced or withheld medical treatment, mass firings, and attacks upon tens of thousands of scientists sparked the formation of a diverse coalition. This coalition includes a mix of liberals, conservatives, and nonpartisans. It’s made up of freethinking parents, students, doctors, nurses, researchers, elected officials, and celebrities.

Many had never before questioned public health narratives or their doctors. Most had blindly supported them. But today, members of this new coalition find themselves probing widely pushed orthodoxy on Covid and beyond, rightly asking what else the media and top public health officials have misled us on.

Now, redemption from the grasp of those who seek to control our health and our lives may come through a collective awakening that’s already begun.

Follow the Science: How Big Pharma Misleads, Obscures, and Prevails,” by Sharyl Attkisson, is now available at bookstores everywhere.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

September 10, 2024 Posted by | Book Review, Corruption, Deception, Science and Pseudo-Science | , | Leave a comment

Did the IRS Manipulate the 2020 Election?

By Jim Bovard | The Libertarian Institute | September 9, 2024

Hunter Biden pled guilty on Thursday to a barrage of federal tax crimes. But will the Internal Revenue Service and Justice Department ever plead guilty to stealing the 2020 election for Joe Biden?

In 2023, the IRS assessed 18,599,109 penalties on individuals who allegedly underpaid or failed to pay federal income taxes. How did the IRS miss Hunter Biden for so long?

In 2021, the Biden administration sought to compel banks to report to the IRS any bank account with more than $600 in transactions per year. But the feds effectively disregarded multimillion dollar windfalls pouring into Hunter’s coffers from around the globe.

Hunter is a tax dodger straight out of IRS Central Casting. Between 2014 and 2019, he pocketed more than $8 million from shady foreign sources, triggering a bushel of Treasury Department Suspicious Activity Reports. Hunter failed to pay more than $1 million in taxes and was slapped by a tax lien of $112,805 for his 2015 taxes. The IRS even threatened to cancel his passport, but no criminal charges were filed.

The IRS began formally investigating Hunter in 2018; by January 2020, a team of a dozen IRS employees were working on his case. The Justice Department failed to file any charges before the statute of limitation expired on Hunter’s 2014 and 2015 tax violations.

IRS investigators vigorously pushed to search part of Joe Biden’s Delaware estate prior to the 2020 election. On September 3, 2020, Assistant U.S. Attorney Lesley Wolf agreed with Gary Shapley, an IRS supervisory special agent, that there was “more than enough probable cause for the physical search warrant” and “a lot of evidence in our investigation would be found in the guest house of former Vice President Biden.” Wolf reportedly told Shapley that U.S. Attorney David Weiss “agreed that probable cause had been achieved.” But Wolf declared that “optics were a driving factor in the decision [not] to execute a search warrant,” according to Shapley.

Like the “optics” Team Biden unleashed when they sent heavily-armed FBI agents to raid Donald Trump’s Mar-a-Lago home in August 2022 to choreograph government documents for photographers? The FBI recently admitted that the documents they seized were arranged prior for a publicity shot. There has been scant media criticism of the Biden White House for seeking to destroy the president’s political opponent with high profile tactics that did better on CNN than in federal court.

IRS investigators were kept out of an October 2020 Justice Department briefing on an alleged “criminal bribery scheme” investigation on Joe Biden and his family. This severely limited the potential political damage to the presidential frontrunner at that time. A female FBI supervisor stated in a congressional interview last year that the Justice Department used the 2022 midterm election as a pretext to delay further action on Hunter’s tax case. CNBC reported in April 2023 that the IRS reportedly “finished its investigation more than a year ago,” but no charges were filed.

The IRS’s Shapley filed a whistleblower complaint in April last year asserting that the investigation of Hunter Biden’s tax violations was being blocked by “preferential treatment and politics.” In May last year, a special agent in the IRS’s international tax and financial crimes group who had spent five years investigating Hunter Biden also filed a whistleblower complaint on the Biden caseThe IRS responded with accusations of criminal conduct and warnings to other agents in an apparent attempt to intimidate into silence anyone who might raise similar concerns,” according to Mark Lytle and Tristian Leavitt, Shapley’s lawyers.

After two IRS officials formally became whistleblowers, the Justice Department dismissed the entire IRS team from the Hunter investigation, potentially crippling the ability to pursue Hunter’s million-dollar plus tax violations.

The U.S. House Ways and Means Committee reported last year that IRS investigators were met with a “‘Delay, Divulge, and Deny’ campaign that ultimately shielded the president’s son by allowing the statute of limitations to expire on several tax crimes for…when Joe Biden was the Vice President.” Attorneys for Hunter Biden were tipped off ahead of time about searches, resulting in the removal or destruction of evidence. “Prosecutors instructed investigators not to ask witnesses questions about Joe Biden or references to the ‘big guy,’” the congressional committee noted.

An FBI agent was interviewed last year by the U.S. House Judiciary Committee investigators regarding the potential coverup. The interview transcript confirms official skullduggery. Just the News website excerpted the transcript of the questioning:

“In September of 2021, are you aware that Lesley Wolf emailed Gary Shapley stating, ‘I do not think you are going to be able to do these interviews as planned,’ adding that they would require approval from DOJ Tax Division. ‘Are you aware of that?’ the FBI agent was asked at one point.

“At another point, the FBI agent was asked: ‘Are you aware in October of 2021 Lesley Wolf emailed Gary Shapley and the investigative team that ‘It will get us into hot water if we interview the President’s grandchildren’?”

In July 2023, the Justice Department sought to close Hunter’s case with a wrist-slap plea for tax misdemeanors. But federal judge  Maryellen Noreika did not agree that ‘there is nothing to see here, move along.’ She asked lawyers a few questions about the blanket immunity that prosecutors provided for Hunter’s other possible crimes and the deal collapsed. Hunter missed his chance to win the Emmy Award for Best Tear-Jerking Performance on Courthouse Steps by a Media Darling. The Washington Post reported that Hunter had written “a statement about his desire to close a difficult chapter in his life, and was planning to read it to news cameras outside the courthouse after entering his plea” at the federal courthouse in Delaware.

Attorney General Merrick Garland claimed that David Weiss, the Special Counsel he appointed to investigate Hunter’s alleged crimes, had independent authority to file charges as he pleased. But it was later revealed that Weiss’ charging ability was severely restricted outside of Delaware and by Justice Department tax attorneys. Curtailing Weiss’ ability to prosecute the case enabled President Biden to continue scoffing at reporters who ask about kickback allegations: “Where’s the money?”

Biden won the 2020 election by a margin of 43,000 votes in three swing states because far more Americans considered Biden “honest and trustworthy” than Trump (52% vs. 40% according to a Gallup poll in October 2020). But Biden’s honesty was always a mirage created by a craven media and federal coverups. Biden campaigning as “Mr. Clean” was as absurd as if Bill Clinton had campaigned as the Chastity Kid, or Donald Trump campaigning as Humility Incarnate.

In the final debate with Trump before the election, Joe Biden proclaimed that “my son has not made money” from China. But while he was vice president, Biden took Hunter with him to Beijing in 2013 to help his boy snare sweetheart deals.

Any tax indictment of Hunter or criminal search of Joe Biden’s Delaware home prior to Election Day 2020 would have shattered Biden’s moral pretenses. And once his Teflon shield vanished, the New York Post’s revelations of Hunter’s laptop would have done far more damage to Uncle Joe.

At the least, a federal search of Biden’s home shortly before the 2020 election could have had the same blunderbuss effect as the October 2016 FBI re-opening of its investigation into Democratic presidential nominee Hillary Clinton’s email crimes.

Hunter’s guilty plea may have been a subsidy for the Kamala Harris presidential campaign. Pleading guilty before the trial got rolling will prevent a deluge of potentially riveting evidence of Biden family corruption and official coverups. Instead, Team Biden and the Harris campaign is hoping for a single news cycle of bad publicity.

The rigging of the Hunter Biden IRS investigation is no surprise to anyone familiar with the agency’s history. As author David Burnham wrote in his 1990 masterpiece A Law Unto Itself: The IRS and the Abuse of Power, “In almost every administration since the IRS’s inception the information and power of the tax agency have been mobilized for explicitly political purposes.” Burnham noted, “The reality that so many are somehow in violation of a supremely murky law gives the agency and the individual agent an astonishingly free hand to pick and choose their targets.” This arbitrary power can be compounded when the feds choose to ignore or overlook brazen tax offenses by the politically connected.

A pardon for Hunter is as certain as Joe Biden’s next verbal hairball. But will federal agencies have the decency to drop the “equal justice” hokum and admit that “optics” trumps fair play almost every time?   

September 9, 2024 Posted by | Civil Liberties, Corruption, Deception, Progressive Hypocrite | , , | Leave a comment

Durov Bombshell: Archaic Crypto Law Charges Reveal French Intel’s Access to Private Communications

By Ilya Tsukanov – Sputnik – 06.09.2024

The Durov saga in France and the continued efforts by countries around the world to crack down on his popular cloud-based, end-to-end encrypted private messenger and social media software has divulged a string of embarrassing details about the sorry state of internet privacy and freedom of information.

Two of the six charges facing Telegram CEO Pavel Durov in France are grounded an obscure, never-used twenty-year-old law obliging companies providing cryptography tools to inform the French Cybersecurity Agency (French acronym ANSSI) and grant it access to the software’s source code and “a description of [its] technical characteristics.”

The 2004 law – uniquely blunt in its demand that companies divulge info about the tech tools used for private communications, is being used against Durov by accusing him of providing encrypted communications services “without certified declaration.”

The legal requirement also means, if it is applied evenly across the board, that the array of instant messengers available to French users, from WhatsApp and Signal to iMessage and the French-made Olvid ‘secure’ messenger used by the French government, do comply with ANSSI regulations, meaning French intelligence can potentially spy on any or all French users at any time.

Adding credence to this idea is the fact that Pavel Durov is reportedly the first-ever tech mogul to be charged under the 2004 law, and the fact that many big-name tech companies have been silent on the Durov case, with the exception of Proton CEO Andy Yen, who characterized the charges against the Russian-born tech mogul as “economic suicide” that’s “rapidly and permanently changing the perception of founders and investors” toward France.

“If sustained, I don’t see how tech founders could possibly travel to France, much less hire in France,” Yen wrote last week.

The law is also reminiscent of the case against WikiLeaks cofounder Julian Assange, who was threatened with decades of jail time by the US under the obscure Espionage Act of 1917, even though that he was not an American citizen, and a publisher, not a spy. Former president Donald Trump was charged under the same act in his classified documents case, which got thrown out by a judge in July.

September 7, 2024 Posted by | Civil Liberties, Corruption, Deception, Full Spectrum Dominance | , | Leave a comment

Hunter Biden’s Guilty Plea: Penance or Plot to Clear Harris of Blot of Biden Family Corruption?

By Ilya Tsukanov – Sputnik – 06.09.2024

President Joe Biden’s son Hunter has pleaded guilty to all nine counts against him in a sprawling, $1.4 million tax evasion case highlighting his history of indulgence in drugs and hookers.

The surprise resolution of the case came just days before opening statements in his trial were set to begin. If it had proceeded, the trial would have likely run through the remainder of Joe Biden’s presidency, and proven politically damaging for the Biden’s successor – Vice President Kamala Harris, just two months out from the November 5 election.

Hunter Biden faces up to 17 years in jail and fines of up to $1.2 million in the tax case, although observers expect leniency for the 54-year-old businessman – whose business allegedly included an elaborate influence-peddling scheme involving the selling of access to his powerful father for cash. Sentencing in the tax case is set for December 16.

The guilty plea adds to Biden’s conviction in a Delaware court in June on three felony counts related to a 2018 handgun purchase, for which he could get up to 25 years in jail. The judge in the case did not set a sentencing date.

Hunter Biden has followed his father like a corruption ball and chain since 2020 when, just weeks from the November election, the New York Post began the publication of a series of stories based on information from his recovered lost laptop about his alleged pay-to-play dealings. The stories threatened to derail the Biden campaign, were it not for social media companies’ move to censor them as ‘Russian disinformation’ – claims which tech execs including Mark Zuckerberg later confirmed were bogus.

The Harris campaign has already made a push to carefully distance itself from Biden on some issues, from capital gains taxes to the Border wall, and may now hope that Biden’s tax charges guilty plea will conclude the Hunter Biden saga, or at least leave him out of the spotlight until safely after the election.

September 6, 2024 Posted by | Corruption | | Leave a comment

Monkeypox – Next p(L)andemic on its way?

August 21, 2024

Christine Anderson, a Member of the European Parliament, has penned an open letter to her fellow citizens:

Dear fellow citizens,

The following text contains some premium conspiracy theories on the subject of “monkeypox”. At least that’s what those who believe in what the TV tells them would claim. But because almost all of the old conspiracy theories have come true in the meantime, we are now getting a new supply:

As you probably know, the WHO has already issued the highest global health alert for monkeypox (Mpox) last week, although the spread is only limited to some regions of Africa.

You probably also know that a simulation game on the topic of “monkeypox” took place at the Munich Security Conference in 2021. One of the participants was Jeremy Farrar, the then director of the billion-dollar health foundation “Wellcome Trust” (funded by the Bill & Melinda Gates Foundation, among others). As luck would have it, Farrar has been Chief Scientist at the WHO since last year.

At the end of 2023, BioNTech enters into a strategic partnership with the Coalition for Epidemic Preparedness Innovations (CEPI). CEPI was founded in Davos in 2016 (WEF sends its regards) and is an alliance of the WHO, the EU Commission, individual governments, pharmaceutical companies, (private) donors and foundations. The “Wellcome Trust”, the Gates Foundation and the UN stand out in the 2024 investor overview.

In May 2024, BioNTech and CEPI announced that they are expanding their portfolio for mRNA vaccines – including vaccines against Mpox. At the same time, the monkeypox vaccine “Imvanex” from “Bavarian Nordic” is already being produced in Denmark and is the only one to be approved in both the EU and the USA.

So much for the crystal-clear facts. If you want to find out more, here is a good place to start: https://www.achgut.com/artikel/kleines_affenpocken_puzzle

In the meantime, during my own research, I came across further, rather disturbing information:

🚑 Did you know that the Austrian Red Cross (Tyrol section) for example, is now looking for new employees for vaccination centers? The tasks include managing patient flows, preparing barcodes and vaccination certificates as well as carrying out mobile vaccinations. Applicants are expected to be “assertive”, among other things. From the end of September, the new employees will receive a gross salary of around €2,450 per month at their place of work in Vienna. https://archive.is/l9CDN

💰 BioNTech previously announced in the German business newspaper Handelsblatt that they expect 90 percent of their total sales to be generated by the end of 2024. https://archive.is/Hhptk

🏗 Currently, BioNTech is building its first commercial African vaccine factory in Rwanda. The focus here also includes mRNA vaccines against Mpox. Some old acquaintances traveled to the opening: EU Commission President Ursula von der Leyen and German Foreign Minister Annalena Baerbock gave themselves the dubious honor. Incidentally, Germany is supporting the development of the vaccine production in Rwanda with almost 36 million euros of German taxpayers’ money. https://archive.is/2Fcqd

⚠️ Dear readers, do you believe in coincidences?
‼️ I DO NOT!

Kind regards,
Yours, Christine Anderson, MEP

September 2, 2024 Posted by | Corruption, Deception | , | Leave a comment

$3,000 and a Toy: Novavax Dangles Incentives to Fill Clinical Trials on COVID Shots for Babies, Kids

By Brenda Baletti, Ph.D. | The Defender | August 29, 2024

Novavax is offering parents up to $3,000 to enroll their children in the vaccine maker’s Phase 2/3 COVID-19 vaccine trial for infants and children ages 6 months to 11 years. The offer also includes a stuffed animal for each child.

The “Hummingbird” trial is testing two primary shots and a booster shot of Novavax’s adjuvanted recombinant spike protein nanoparticle vaccine in children. The study, which began in 2022, is enrolling 3,600 children.

The study, which began in the U.S., is expected to run through 2025 and will be conducted in the U.S. and other countries.

The children will receive three injections and visit the clinic eight times. Parents will participate in three phone calls and keep an e-diary of the vaccine’s effects on their child. Some children will receive two additional injections, for a total of five shots.

The study website promises, “You will be compensated for your time and travel regardless of your immigration status. Transportation to the study site may also be provided, as available. No health insurance is required to participate.”

Recruitment materials from Be Well Clinical Studies, which is running one of the U.S. trials, state that compensation can be more than $3,000 over two years.

A 2023 video explaining the study also promises incentives for the children, including “a Covid stuffed animal.”

In the video, a pastor from Louisiana who has four children enrolled in the study said incentives like the stuffed animal made the kids even “more excited than the parents” to participate.

The video features Dr. Jibran Atwi who is running a Hummingbird trial in Lafayette, Louisiana. He encouraged people to participate in the study, because COVID-19 severely affected kids, particularly through lockdowns and lost schooling.

Atwi also said that COVID-19 can be “very disruptive” because if a child has to stay home from school, parents may not be able to go work and the child may have to be isolated from their grandparents.

“Prevention,” he said, “is the best medicine.” He added that there had been an “impressive response” from parents who wanted to participate.

Research shows that young children rarely get sick from COVID-19 and that the illness is typically mild in older kids.

Atwi received over $2 million in research funding in 2023 from Big Pharma, according to the Open Payments website.

Most of that funding came from Genzyme — a Sanofi subsidiary — and from Sanofi, which shares the co-exclusive licensing agreement with Novavax to commercialize its COVID-19 vaccine.

In 2022, Atwi received over $1 million, largely from AstraZeneca and Genzyme.

Last week, the U.S. Food and Drug Administration (FDA) granted emergency use authorization to Pfizer and Moderna’s 2024-2025 mRNA COVID-19 shots, but Novavax’s 2024-2025 formula has not yet been authorized.

The FDA has authorized previous versions of the Novavax vaccine, but only for children ages 12 and up.

High payments place children ‘at risk of coercion’

Other pharmaceutical companies that have paid research subjects large sums of money have come under scrutiny. In the United Kingdom (U.K.), Moderna was criticized for initially offering children’s families 1,505 pounds ($1,984 dollars) to participate in its NextCOVE clinical trial, which is testing Moderna’s mRNA vaccine in children ages 12 and up.

The Children’s Covid Vaccine Advisory Council submitted a complaint to the U.K.’s Prescription Medicines Code of Practice Authority (PMCPA) — an industry trade group that regulates ethical practices — raising concerns about “inappropriate financial inducement” offered to children and their parents to participate in the trial.

The council cited concerns raised by the research ethics committee (REC) that approved the clinical study. Regarding the 1,500-pound payment they wrote:

“This amount seems much higher than what would be considered a reasonable reimbursement and therefore would contravene clinical trial regulations. The Medicines for Human Use (Clinical Trials) Regulations (2004) explicitly prohibit the giving of incentives or financial inducements to children… or their parents.”

The REC said the amount, “placed the children at risk of coercion,” and the organization required that Moderna reduce the offer before recruitment could begin. Moderna reduced the amount to 185 pounds ($244 dollars).

Yet, according to the complaint, at least one pediatrician continued to offer the high enrollment compensation.

The PMCPA sanctioned Moderna, and the case report on the issue is currently pending.

If the PMCPA determines a pharmaceutical company has breached the industry code, it can require the company to pay administrative charges or issue a corrective statement. Or, it may request a compulsory audit of the company.

In the U.S., Be Well is also advertising that it will pay parents $2,400 for enrolling their infants and toddlers, ages 5-23 months, in Moderna’s Rhyme Trial for an mRNA RSV and a human metapneumovirus (hMPV) vaccine.

According to the clinicaltrials.gov website, Be Well withdrew from the Moderna RSV study, but the website is still advertising to recruit participants.

Be Well is run by founder and director Dr. Mark Carlson, a geriatrician, who has taken nearly $3 million in research funding from Big Pharma, mostly from Moderna, since 2021.

Moderna did not respond to The Defender’s inquiry about compensation offered to children’s families to participate in these studies.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 30, 2024 Posted by | Corruption, Video | , , | Leave a comment

The Energy Transition Ain’t Happening: “Clean Fuels”

By Francis Menton | The Manhattan Contrarian | August 19, 2024

Come here for the latest news on how the so-called “energy transition” is grinding to a halt. No amount of government handouts can make this ridiculously uneconomic fantasy work. My last post on the subject, on July 20, reported on the collapse of a large “green hydrogen” project in Australia, with the stated loss of an investment of about $2 billion (Australian) (equivalent to about $1.3 billion U.S.).

It seems that that one was just the tip of the iceberg. Today’s Wall Street Journal has a substantial roundup of the financial status of a half-dozen or so so-called “clean fuel” projects. The headlines from the print and online versions tell you what you need to know. In the print edition (page B3) it’s “Clean-Fuel Startups Begin to Fizzle Out.” Online, it’s “Clean Fuel Startups Were Supposed to Be the Next Big Thing. Now They Are Collapsing.” As the headlines indicate, pretty much all of these “clean fuels” ventures are failing. Who could have guessed?

The Journal’s label of “clean fuels” is used to cover two different categories, one being biofuels, and the other being so-called “green hydrogen” (the stuff produced by electrolysis of water using electricity produced by wind or sun). The biofuels category appears to include such genius ideas as making fuel for airplanes or ships out of used cooking grease. Whatever you might think of that idea, these are still carbon-based fuels, and it’s not clear to me at all why they are supposedly “cleaner” than other carbon-based fuels like petroleum or natural gas.

Hydrogen, on the other hand, offers the promise of providing energy for planes, trains, ships and automobiles free of the dreaded “carbon emissions.” Just hook up some solar panels or wind turbines to big electrolyzers and watch the stuff bubble out of the water virtually for free! The badly misnamed “Inflation Reduction Act” made billions upon billions of dollars of subsidies available for these kinds of projects. Surely the successes should be rolling forth one after the other by this time.

It turns out that no matter how many subsidies the government doles out, nobody can make this “green” hydrogen stuff as cheaply as natural gas can be produced by drilling into rock.

One of the big green hydrogen startups is called Plug Power. The Journal quotes its CEO, Andy Marsh:

“The excitement of the early days has not lived up to the hype,” said Andy Marsh, chief executive of Plug Power, a startup that recently opened one of the country’s first plants making green hydrogen, a potential replacement for fossil fuels in industries such as steel making and chemical production. Shares of Plug Power have tumbled more than 90% since the passage of the U.S. climate law two years ago.

Well, at least they’re not bankrupt — yet. You do have to wonder how Mr. Marsh could qualify to be a CEO of such a company and raise hundreds of millions of investor dollars without ever crunching the numbers to realize that green hydrogen could never be economical. Could it be that his business plan all along was to pay himself a big salary out of the investors’ funds and then walk away when the inevitable bankruptcy came?

Here are a couple of paragraphs from the Journal summarizing the overall state of the industry:

Many clean-fuel projects have become money pits, in part because of the great amounts of power they need. High interest rates, supply-chain disruptions and expensive power-grid upgrades have driven up electricity prices. . . . “The only way to fix it is by lowering the cost of green electricity,” said Andrew Forrest, one of the most vocal advocates of hydrogen.

Wait a minute. Andrew Forrest — where have we heard that name? Oh, he is the Australian tycoon who goes by the name “Twiggy.” He’s the head of the company Fortescue, and was the subject of my July 20 post as a result of the collapse of his big Australian green hydrogen project. The Journal goes on to some detail about “Twiggy’s” ongoing green hydrogen plans:

Forrest, the billionaire founder of Australian iron-ore giant Fortescue, said his company’s 2030 hydrogen production target now looks unrealistic. Fortescue is planning to produce its own clean power to make hydrogen in Australia and is considering doing the same in Arizona.

But somehow the Journal fails to mention the failure of Forrest’s big Australian project. Could it be that they interviewed him a month ago, before that happened?

So the odds are that nobody will ever be able to make these “clean fuels” economically. The consequence:

Without clean fuels, emissions at many companies are expected to keep climbing, threatening U.S. and global climate targets. Industries including aviation and shipping are counting on the new fuels because wind and solar power and batteries can’t meet their huge energy needs.

When are we allowed to declare that this whole charade is over?

UPDATE, August 20: Commenter Pablo Honey suggests that it might be interesting to look at the financials for one of these “clean fuels” companies. Here is the 2Q 24 earnings release for Plug Power, just out on August 8. Some key figures: revenue — $143.4 million; “earnings” — net loss of $262.3 million.

Margins: “The Georgia plant’s increased production capacity and strategic price increases across the hydrogen product portfolio have significantly improved hydrogen margins.” So they are increasing prices from levels that were already a multiple of the price of natural gas for equivalent energy content. Good for them if they can get someone to pay, but that inherently means that their market is limited to buyers who either need hydrogen for its non-energy properties (i.e., fertilizer) or ones who are willing to forego profit out of religious devotion to “decarbonization.”

Government handouts: “Plug Power became one of the first companies to leverage the PTC [Production Tax Credit] for its liquid hydrogen plant in Georgia, optimizing financial performance and enhancing shareholder value. . . . Plug Power is progressing with the DOE loan, which aims to support the expansion of its green hydrogen initiatives and infrastructure for up to six sites.” Great — it’s another Solyndra in the works.

August 25, 2024 Posted by | Corruption, Malthusian Ideology, Phony Scarcity | | Leave a comment

What’s Really Happening with Mpox

The Mpox Emergency

By David Bell | Brownstone Institute | August 18, 2024

The World Health Organization (WHO) acted as expected this week and declared Mpox a Public Health Emergency of International Concern (PHEIC). So, a problem in a small number of African countries that has killed about the same number of people this year as die every four hours from tuberculosis has come to dominate international headlines. This is raising a lot of angst from some circles against the WHO.

While angst is warranted, it is mostly misdirected. The WHO and the IHR emergency committee they convened had little real power – they are simply following a script written by their sponsors. The African CDC, which declared an emergency a day earlier, is in a similar position. Mpox is a real disease and needs local and proportionate solutions. But the problem it is highlighting is much bigger than Mpox or the WHO, and understanding this is essential if we are to fix it.

Mpox, previously called Monkeypox, is caused by a virus thought to normally infect African rodents such as rats and squirrels. It fairly frequently passes to, and between, humans. In humans, its effects range from very mild illness to fever and muscle pains to severe illness with its characteristic skin rash, and sometimes death. Different variants, called ‘clades,’ produce slightly different symptoms. It is passed by close body contact including sexual activity, and the WHO declared a PHEIC two years ago for a clade that was mostly passed by men having sex with men.

The current outbreaks involve sexual transmission but also other close contact such as within households, expanding its potential for harm. Children are affected and suffer the most severe outcomes, perhaps due to issues of lower prior immunity and the effects of malnutrition and other illnesses.

Reality in DRC

The current PHEIC was mainly precipitated by the ongoing outbreak in the Democratic Republic of Congo (DRC), though there are known outbreaks in nearby countries covering a number of clades. About 500 people have died from Mpox in DRC this year, over 80% of them under 15 years of age. In that same period, about 40,000 people in DRC, mostly children under 5 years, died from malaria. The malaria deaths were mainly due to lack of access to very basic commodities like diagnostic tests, antimalarial drugs, and insecticidal bed nets, as malaria control is chronically underfunded globally. Malaria is nearly always preventable or treatable if sufficiently resourced.

During this same period in which 500 people died from Mpox in DRC, hundreds of thousands also died in DRC and surrounding African countries from tuberculosis, HIV/AIDS, and the impacts of malnutrition and unsafe water. Tuberculosis alone kills about 1.3 million people globally each year, which is a rate about 1,500 times higher than Mpox in 2024.

The population of DRC is also facing increasing instability characterized by mass rape and massacres, in part due to a scramble by warlords to service the appetite of richer countries for the components of batteries. These in turn are needed to support the Green Agenda of Europe and North America. This is the context in which the people of DRC and nearby populations, which obviously should be the primary decision-makers regarding the Mpox outbreak, currently live.

An Industry Produces What It Is Paid for

For the WHO and the international public health industry, Mpox presents a very different picture. They now work for a pandemic industrial complex, built by private and political interests on the ashes of international public health. Forty years ago, Mpox would have been viewed in context, proportional to the diseases that are shortening overall life expectancy and the poverty and civil disorder that allows them to continue. The media would barely have mentioned the disease, as they were basing much of their coverage on impact and attempting to offer independent analysis.

Now the public health industry is dependent on emergencies. They have spent the past 20 years building agencies such as CEPI, inaugurated at the 2017 World Economic Forum meeting and solely focused on developing vaccines for pandemic, and on expanding capacity to detect and distinguish ever more viruses and variants. This is supported by the recently passed amendments to the International Health Regulations (IHR).

While improving nutrition, sanitation, and living conditions provided the path to longer lifespans in Western countries, such measures sit poorly with a colonial approach to world affairs in which the wealth and dominance of some countries are seen as being dependent on the continued poverty of others. This requires a paradigm in which decision-making is in the hands of distant bureaucratic and corporate masters. Public health has an unfortunate history of supporting this, with restriction of local decision-making and the pushing of commodities as key interventions.

Thus, we now have thousands of public health functionaries, from the WHO to research institutes to non-government organizations, commercial companies, and private foundations, primarily dedicated to finding targets for Pharma, purloining public funding, and then developing and selling the cure. The entire newly minted pandemic agenda, demonstrated successfully through the Covid-19 response, is based on this approach. Justification for the salaries involved requires detection of outbreaks, an exaggeration of their likely impact, and the institution of a commodity-heavy and usually vaccine-based response.

The sponsors of this entire process – countries with large Pharma industries, Pharma investors, and Pharma companies themselves – have established power through media and political sponsorship to ensure the approach works. Evidence of the intent of the model and the harms it is wreaking can be effectively hidden from public view by a subservient media and publishing industry. But in DRC, people who have long suffered the exploitation of war and the mineral extractors, who replaced a particularly brutal colonial regime, must now also deal with the wealth extractors of Pharma.

Dealing with the Cause

While Mpox is concentrated in Africa, the effects of corrupted public health are global. Bird flu will likely follow the same course as Mpox in the near future. The army of researchers paid to find more outbreaks will do so. While the risk from pandemics is not significantly different than decades ago, there is an industry dependent on making you think otherwise.

As the Covid-19 playbook showed, this is about money and power on a scale only matched by similar fascist regimes of the past. Current efforts across Western countries to denigrate the concept of free speech, to criminalize dissent, and to institute health passports to control movement are not new and are in no way disconnected from the inevitability of the WHO declaring the Mpox PHEIC. We are not in the world we knew twenty years ago.

Poverty and the external forces that benefit from war, and the diseases these enable, will continue to hammer the people of DRC. If a mass vaccination campaign is instituted, which is highly likely, financial and human resources will be diverted from far greater threats. This is why decision-making must now be centralized far from the communities affected. Local priorities will never match those that expansion of the pandemic industry depends on.

In the West, we must move on from blaming the WHO and address the reality unfolding around us. Censorship is being promoted by journalists, courts are serving political agendas, and the very concept of nationhood, on which democracy depends, is being demonized. A fascist agenda is openly promoted by corporate clubs such as the World Economic Forum and echoed by the international institutions set up after the Second World War specifically to oppose it. If we cannot see this and if we do not refuse to participate, then we will have only ourselves to blame. We are voting for these governments and accepting obvious fraud, and we can choose not to do so.

For the people of DRC, children will continue to tragically die from Mpox, from malaria, and from all the diseases that ensure return on investment for distant companies making pharmaceuticals and batteries. They can ignore the pleading of the servants of the White Men of Davos who will wish to inject them, but they cannot ignore their poverty or the disinterest in their opinions. As with Covid-19, they will now become poorer because Google, the Guardian, and the WHO were bought a long time back, and now serve others.

The one real hope is that we ignore lies and empty pronouncements, refusing to bow to unfounded fear. In public health and in society, censorship protects falsehoods and dictates reflect greed for power. Once we refuse to accept either, we can begin to address the problems at the WHO and the inequity it is promoting. Until that time, we will live in this increasingly vicious circus.

David Bell, Senior Scholar at Brownstone Institute, is a public health physician and biotech consultant in global health. He is a former medical officer and scientist at the World Health Organization (WHO), Programme Head for malaria and febrile diseases at the Foundation for Innovative New Diagnostics (FIND) in Geneva, Switzerland, and Director of Global Health Technologies at Intellectual Ventures Global Good Fund in Bellevue, WA, USA.

August 18, 2024 Posted by | Corruption, Deception, Mainstream Media, Warmongering, Science and Pseudo-Science | , , | Leave a comment

The Academic Whistleblower

A Human Sacrifice Worth Making?

By Lisa Hutchinson | Health Advisory & Recovery Team | August 14, 2024

Recently, I listened to an interview with Dr Carl Elliott based on his published book released in June 2024 titled “The Occasional Human Sacrifice: Medical Experimentation and the Price of Saying No”. Dr Elliott is a bioethicist at the University of Minnesota who was trained in medicine as well as philosophy. For years, he fought for an independent inquiry into a case of corruption at a psychiatric research study at his own university in which sadly an especially vulnerable patient lost his life. Carl experienced first hand what it is like to be an academic whistleblower, and endured a terrible experience. His own efforts resulted in him being shunned by his friends and colleagues and impeded by his own university, who denied any wrongdoing, until an independent state investigation finally vindicated his claims after a 7-year-long battle.

Carl posits that As mentioned, his foray into this is very sad and disturbing. He detailed the extraordinary case of a mentally vulnerable man, Dan Markingson, who was admitted to a psychiatric unit after experiencing a series of psychotic episodes. Despite being a danger to himself and others, he was enrolled on a clinical trial of a new multi-drug regimen. Dan was coerced into following the treatment decisions of his psychiatrist, but against the strong objections of his concerned mother, he entered the study because he gave his “consent”. Worried for his safety, Dan’s mother spent several months trying to get him out of the study, after his behaviour dramatically worsened. She wrote to the study centre and study coordinator to ask to remove her son from the study. Despite her justified concerns, she was ignored. Tragically, several months later in the Spring of 2004, Dan killed himself in extreme circumstances.

Carl discussed several stories of how participants of medical research can be deceived into taking part in experimental programmes they do not understand, even in circumstances when the mortality risks are high. Many patients are coerced into studies with blatant financial conflicts of interest or industry funding. When Carl learned of Dan’s case and raised concerns he could not get anyone to take him seriously, so he decided to do his own research and publish a book. By bringing this issue to a broader audience, Carl hoped it would prompt the university into doing something, but this failed spectacularly, and he became a despised figure in his own academic centre.

After learning of Dan’s case in 2008, Carl spent 7 years trying to get Dan’s death investigated. His efforts included creating petitions, writing to the University Alumni, writing to the FDA and federal government. Eventually, he got a state investigation, and although the ruling was positive and vindicated everything he and other critics raised, the follow up was non-existent. His efforts accomplished very little – there was no apology from the academic university, no compensation to victims, no reform, or sanctions for the wrongdoers or efforts to learn from the devastating situation. This was a demoralising ending after such a long struggle.

Ethical standards and integrity have been gradually compromised for several decades. It is unclear why there is pressure to violate ethical rules in the medical research domain. Some of the reasons are financial, but perhaps a bigger issue is the pursuit of glory for some academic clinicians. In psychiatry, balancing the interests of individual participants in trials versus the pursuit of scientific answers is compromised. In 90% of the scandals Carl teaches about at the University of Minnesota, trial participants are mentally ill, disabled, have low socioeconomic status, are vulnerable, and cannot look out for themselves – collective traits that are exploited. As he describes it, the ‘honour code’ in medicine should safeguard and offer protections for such patient groups.

Many whistle-blower stories in the 1970s and 1980s predate the rise of the Big Pharma trials of today. Among clinicians and academics there is a race for glory, status, academic promotion, awards, and prizes. In the 1990s, the financial status changed unrecognisably with recent scandals having huge money stakes, absent from earlier corruption cases. In the past 20-30 years, academic research is less about patient care and more about research funding, which is a toxic situation. Sectors outside medicine have a regulatory system, which is absent in medical research. Instead, an ‘honour’ system exists in which professionals are trusted to behave honestly. Ultimately, there is a quasi regulatory responsibility by industry for overseeing integrity in its multi-billion dollar sector. Coupled with medical arrogance, bioethics within academic centres is now funded by the same industry players funding the studies. Thus, bioethics has been absorbed into academic health centres, relocating ethics to the belly of the beast!

There is a huge difficulty in maintaining independence and not being ‘captured’ by academic medicine. When research funding for academic salaries or tenure is through government-led institutions combined with the pressure to publish findings in high-profile medical journals, this creates a dangerous authoritarian culture. Such an environment has sometimes led to the dehumanisation of the patient, and maintaining ethical standards is a challenge. In a fee-for-service culture where high financial incentives exist, dismissing adverse effects of experimental treatments and lowering the inclusion criteria threshold are all too pervasive. There are of course well-intentioned medical professionals, but corporate overlords, dependence on practice guidelines coupled with the tremendous academic workload, stymies patient safeguarding and forges academic burnout.

What do whistleblowers have in common? They are motivated by honour, integrity, and moral concerns. They have no expectation for financial gain and they do not derive any personal advantages for themselves; in fact, they usually have everything to lose, such as financial stability and reputational damage, yet they still speak out. The reason many whistleblowers persisted in what they felt was a near futile struggle for years or even decades before resolution, was they were tenacious and refused to give up. Notably, cases known to the public are only examples in which a ‘resolution’ was achieved, even though the whistleblowers had reputational damage and no apology or financial compensation for victims was provided. So the situation is likely worse in terms of the treacherous path travelled by many whistleblowers, as we only hear of the most ‘successful’ cases.

Whistleblowers who worked for the public health sector often got nowhere. All whistleblowers had a common metaphor – if they were to look in the mirror, could they live with themselves if they did not do something? Many experience a form of PTSD and none experience improved lives following their exposure. Does disillusionment occur prior to whistleblowing, or when attempts or reports are ignored? Sadly, it seems there is a slow descent into nihilism. Most whistleblowers believe that if the outside world knew what they knew, this would encourage people to defend or change the corruption – notably this never happens. They also hope that close friends or relatives will stand by them, but in its absence, an existential break occurs.

Some whistleblowers feel a sense of guilt because of their complicity in their own industry. Others feel guilt out of a sense of disloyalty to their peers or not wanting to expose an entire institution into disrepute. The notion that whistleblowers are heroic victorious figures that embark on a ‘David versus Goliath’ image is a falsehood! Perhaps the whistleblower is a rare breed; many who are concerned might be more realistic or disillusioned to begin with, so have a lower expectation in terms of likely justice. Possible reasons there are not more whistleblowers is because they know their action would be futile, they could get disciplined, they did not want to snitch on friends or colleagues, or they had a (misplaced) loyalty to their institution. Indeed, a recent BMA survey reported that 61% of doctors polled about patient safety concerns would not raise concerns because of fears that they or their colleagues might be “unfairly blamed or suffer adverse consequences”.

Organisational loyalty is puzzling because an institution intrinsically seems to instil loyalty, but fighting something that undermines it, ironically goes against those who expose it. One way to address this would be to establish independent organisations to investigate such cases. Although many are aware bad behaviour exists, those in senior leadership positions do not ask, so the corruption remains under the radar. One example was at the Karolinska Institute over lethal synthetic trachea transplants, in which a surgeon had falsified results and misled the hospital about the health of those who received the transplants. While the surgeon involved, Paolo Macchiarini, received a prison conviction, the Swedish legal authorities and Karolinska Institute did not apologise to whistleblowers or compensate the victims. This high-profile case did not tarnish the institute’s reputation; in fact, it is rare for institutions to suffer in medical corruption cases. Leaders at academic institutions worry that if problems are exposed, it will deleteriously impact them, so silence or internal handling is considered the best policy.

One would think it would be better to come clean so that things can be remedied, and the error not repeated, in the hope wrongdoers are punished and institutions reformed. However, in his research and experience, Carl has never come across an institution that took positive resolution steps. Academic organisations still attack anyone who threatens their reputation. Often the senior figures in such scandals, such as Deans, Presidents or Directors, have left by the time a scandal is exposed, which one might think would help reduce any reputational damage. Although no one currently employed would be implicated in such scandals if the culprits have departed, the corrupt behaviour remains unchanged, so it is hard to offer an explanation.

The general public has a high opinion of doctors, believing medical professionals have strong ethics and want to help people and save lives. While this is true for many doctors, modern medicine has become big business financially. Patients are nowadays consumers, which is an inevitable slide into corruption. The marketing of medical devices and drugs has become more covert, such as  bribes given to doctors. The scandals involved to preserve the illusion of integrity internally and externally are egregious. Carl is sceptical that a greater awareness of Big Pharma and how their marketing efforts operate would result in a more-positive outcome.

Ultimately, drug representatives are salesmen: they try to get doctors to prescribe their drugs. For many years, the vast majority of marketing was aimed at doctors not patients, although direct-to-consumer advertising is now ubiquitous. Huge financial sums are at stake, and most doctors do not like to imagine their prescription decisions are influenced by Big Pharma. Drug representatives have developed relationships with doctors – they are mercenaries. In the blockbuster drug era, especially in the USA, it is possible to make billion dollar drug sales for chronic illnesses, and doctors can be exploited to earn millions. Other than consultancy, doctors can receive lavish gifts, such as expensive dinners or premium tickets to expensive events. In the 1990s, the development of script tracking enabled the ability to measure in real time how marketing efforts affected doctors script sales. All drug representatives have access to the same data, so they compete for doctors with highest prescriber practices.

Ultimately, all the systems follow the same money trail. People who run the hospitals are worse, and according to Carl, those getting most from industry have the largest bribes. This farce is omnipresent; alarmingly, many bioethicists are not averse to taking industry money, highlighting that we are falling off the bioethics cliff. It is striking how universal and commonplace the language of medicine has become to describe the human experience. People define themselves on the basis of a medical diagnosis, illustrating how marketing has infiltrated our lives. For instance, people describe medical interventions as the person they are inside and how this fulfils their authentic self. It is an illusion that an intervention helps you become who you really are on the inside. Carl suggests pressure exists either to fit in or to stand out, which are two sides of the same coin.

Does bioethics have a rescue philosophy? In general, bioethics is a huge disappointment, with the status quo unchanged since the 1980s. Bioethics has taken up residence in academic health centres and is controlled by the same corrupt forces. It is sobering that not a single medical research scandal exists, whether patient care, sexual abuse, or research misconduct, in which a bioethicist has criticized their own institution. They know how unwelcome it would be, so they keep quiet! The conclusions of Carl’s book and interview are disheartening: being a whistleblower is not worth the hassle or personal devastation involved for the noble individuals who speak out. Since the Covid era, whistleblowers have become more prolific as many no longer accept the associated injustice. Let’s hope this seeds change and a much-needed new cultural shift to inspire and support future academic whistleblowers rather than deter them. The brave but solitary path of the academic whistleblower must be a human sacrifice worth taking!

August 15, 2024 Posted by | Book Review, Corruption, Science and Pseudo-Science, Timeless or most popular | | Leave a comment

White House Suppressed Docs Showing Hunter Sought State Dept Help for Burisma

By Kyle Anzalone | The Libertarian Institute | August 14, 2024

Newly released documents show that Hunter Biden sought to inappropriately benefit the Ukrainian energy company Burisma while his father was vice president. The records were suppressed by the White House.

The files, obtained by the New York Times and reported on Tuesday, show Hunter sent a letter to the US ambassador in Italy in 2016 requesting assistance for Burisma. At the time, Hunter was making tens of thousands of dollars per month as a board member of the Ukrainian energy company, a position he was handed in 2014.

The diplomatic staff in Italy felt the request was not appropriate. “I want to be careful about promising too much,” an official based at the US Embassy in Rome wrote. “This is a Ukrainian company and, purely to protect ourselves, [the US government] should not be actively advocating with the government of Italy without the company going through the [Department of Commerce] Advocacy Center.”

While the Times received records from the State Department, the outlet was not provided with the full text of the letter. The paper suggested the State Department may have more records related to Hunter Biden that it is withholding, also noting the documents it obtained were only released “after President Biden dropped his re-election bid.”

Abbe Lowell, a lawyer for Hunter, claimed nothing untoward took place, maintaining he merely “asked various people” to arrange a meeting with the governor of Italy’s Tuscany region, where Burisma was “pursuing a geothermal project.” The White House claims President Biden was “not aware” of Hunter’s outreach to the embassy in Italy at the time, according to the Times.

As Joe Biden campaigned for the White House in 2020, questions arose about his son’s ties to Burisma – a major gas firm founded by Ukrainian oligarch and ex-environment minister Mykola Zlochevsky. At the time, Hunter sat on the company’s board and raked in between $50,000 and $83,000 each month, despite having no prior experience in the energy sector or in Ukraine more broadly. Then VP under the Obama administration, the elder Biden was directing US policy in Ukraine when Hunter got the job. The country was in a state of instability and civil war following a US-backed coup in 2014.

The Biden campaign and White House have attempted to dismiss charges that Hunter acted inappropriately and exploited his father’s political influence, deeming the claims Russian disinformation.

August 14, 2024 Posted by | Corruption, Deception | , , | Leave a comment

Georgia lays blame for 2008 war with Russia

RT | August 14, 2024

Former Georgian president Mikhail Saakashvili was responsible for the country’s conflict with Russia in 2008, and acted on instructions from external forces, the ruling party in the former Soviet state has said.

The five-day war erupted on the night of August 8, 2008, when US-backed Saakashvili sent troops into Georgia’s breakaway region of South Ossetia, shelling a base used by Russian peacekeepers who had been in the republic since the 1990s.

Then Russian President Dmitry Medvedev ordered a “peace enforcement” operation in response, which led to the defeat of Tbilisi’s forces. On August 26, Moscow recognized the independence of South Ossetia and another breakaway region, Abkhazia.

The political council of the ruling Georgian Dream party said in a statement on Tuesday that a public legal process was necessary to establish “who committed a treacherous crime against our country and people [in 2008].” This was required in the interests of long-term peace and stability, the party stated.

“The majority of Georgian society rightly doubts Saakashvili’s adequacy. However, the fact is that Saakashvili’s reckless actions in August 2008 were not a result of his mental instability, but a result of the instructions from the outside and a well-planned betrayal,” the statement read.

Georgian Dream did not identify the external forces that it claims directed the actions of the Georgian president 16 years ago.

Last week, Georgian Prime Minister Irakli Kobakhidze said the government would address the Prosecutor’s Office, the Constitutional Court, or set up a parliamentary commission to look into the events of 2008. According to Kobakhidze, Saakashvili, who is serving a six-year prison sentence, could face additional charges of treason over his role in the conflict with Russia. Such an offense carries a maximum punishment of life in prison.

Saakashvili was voted out of office in 2013 and fled to the US. He also has a Ukrainian passport, which he obtained during a brief stint as governor of the country’s Odessa Region in 2015-16.

The former president was detained in October 2021 after secretly returning to Georgia during an election in the country. The authorities in Tbilisi accused Saakashvili of abuse of power, organizing attacks on political opponents, embezzlement, and other offenses during his time in office between 2004 and 2013.

The 56-year-old has remained in hospital in the Georgian capital since March 2022 due to deteriorating health. Saakashvili insists that the prosecution is politically motivated. His lawyers claim that the politician, who has lost a significant amount of weight in custody, is not receiving adequate medical care.

August 14, 2024 Posted by | Corruption, Militarism | | Leave a comment

‘They Have to Be Stopped’: Woman Says COVID Hospital Protocols Caused Husband’s Death

By Michael Nevradakis, Ph.D. | The Defender | August 8, 2024

In June 2021, 61-year-old Jeffrey R. Smith was healthy, active and enjoying his 42nd year of marriage to Sharon Smith. That same month, they both came down with COVID-19, but their symptoms were mild and there was little cause for concern.

When Jeffrey’s symptoms lingered just a bit longer than those of his wife, he visited an urgent care center.

That visit marked the beginning of a 39-day ordeal that resulted in his hospitalization, a loss of 47 pounds, and, ultimately, his death, on Aug. 11, 2021, at Mease Countryside Hospital in Safety Harbor, Florida.

Jeffrey’s cause of death was officially listed as COVID-19. But when Sharon examined his approximately 6,000 pages of medical records, she discovered he had sustained kidney damage, likely due to repeated doses of medications including remdesivir, a drug known to stop kidney function in patients.

Sharon also discovered that doctors at the hospital did not treat her husband’s pulmonary embolism — or blood clot — which he developed during his hospitalization. Instead, she alleges doctors insisted she allow him to be placed on a ventilator and that she sign a do not resuscitate (DNR) order for him.

In an interview with The Defender, Sharon said the treatment her husband received at the hospital was incentivized by the Centers for Disease Control and Prevention’s (CDC) COVID-19 hospital protocols — and by the fact that neither she nor her husband had received a COVID-19 vaccine.

Sharon shared extensive documentation with The Defender to corroborate her story.

‘He didn’t give his consent to anything’

On July 4, 2021, Sharon said she “just didn’t think my husband was breathing as deep as I was.” Out of concern, she recommended they visit a local urgent care center for a chest X-ray.

“When we went to urgent care and they checked his blood pressure, everything was normal,” Sharon said. However, the couple was sent to Mease Countryside Hospital for X-rays.

Sharon recalled that she could not stay at the hospital due to COVID-19 restrictions, but was told she could return in two hours to pick up her husband. However, about 30 minutes later, her husband called and said the hospital was going to keep him overnight.

“I said, why?” Sharon recalled. “He wasn’t struggling to breathe. … Blood pressure was good, temperature was good.” Despite this, Sharon was told that her husband was going to be kept “on a little oxygen.”

“What we didn’t know at the time was that they had given him two doses of remdesivir, and he didn’t give his consent to anything,” Sharon said. Doctors administered the two doses within three hours of admitting Jeffrey to the hospital.

He had a D-dimer test for pulmonary embolisms, and it was normal, Sharon said. “Everything was normal. He was so healthy going in. He took no medications, had no health issues at all. He walked three to six miles a week. We just had our checkup at the doctor. So, there was nothing there.”

Later that evening, Sharon said someone from the hospital called “in a panic, in the middle of the night … that they had to move Jeff up to the COVID ICU [intensive care unit] to just observe him a little bit more.”

The following day, Sharon said a doctor told Jeffrey that he was “probably going to have to go on the ventilator.” According to Sharon, when he asked why he had to be ventilated when he had come to the hospital for a chest X-ray — and mentioned that his wife would not agree to this — he was told “Well, your wife is going to have to like this or you’re going to die.”

“I said, ‘Oh my goodness, you’re not going to die.’ First of all, because we trusted the doctors, we trusted the hospital. We never in our wildest imaginations thought that you would go in for anything and they would try to harm you, but that’s exactly what they did,” Sharon told The Defender.

As time went on, the doctors gave him more and more oxygen, and more and more drugs, Sharon said, although she wasn’t informed about it. She only learned about the medications when she reviewed Jeffrey’s medical records after his death.

“The drugs that they were giving him … Precedex, propofol, fentanyl, midazolam … these are the drugs that they use to euthanize people,” Sharon said.

‘They stopped feeding him, giving him any kind of water, cleaning him’

Sharon said there were other examples of the hospital mistreating her husband.

“They stopped feeding him, giving him any kind of water, cleaning him,” she said, recalling that during a FaceTime conversation, he looked “awful.”

“I said, ‘Have you had a shower? Have they washed?’ He goes, ‘No, they haven’t.’ He looks awful. His hair’s a mess. He’s unshaven and he hasn’t had his bedding changed in a week. He hasn’t got any different clothes on,” Sharon recalled.

Her husband urged her not to make an issue of it, according to Sharon.

“When I would say something to the nurses, Jeff would say, ‘Sharon, don’t make waves, because they’re taking it out on me.’ And at the time, I didn’t understand. I didn’t think they were doing bad things, purposely doing bad things to him. I thought they were just being neglectful,” she said.

Sharon said it was difficult to speak to a doctor or to get authorization to visit Jeffrey.

“Every day I would say, I want the doctor to call me. The doctor would call me. Sometimes they were rude to me, sometimes they were short with me, some were OK.” She had to “plead” with a hospital administrator in one instance to be allowed a 15-minute visit.

“I got up there to see Jeff, and he was just a mess. I mean, they weren’t getting him out of the bed. He was just deteriorating in front of my eyes,” Sharon recalled.

On another occasion, Sharon said she was allowed a visit for “17 minutes, exactly” and was told she would soon be permitted daily visits. Later that day, Sharon called to check on Jeffrey and was told he was “relaxed and had some ice cream.”

A half-hour later, “I get a call from the hospital and it’s a panic … they said, ‘We’re going to put Jeff on the ventilator right now. He had a panic attack and his oxygen level dropped and he can’t get it back up, so we have to put him on the ventilator.’”

Sharon said she was offered the opportunity to speak with Jeffrey via FaceTime. “I got 20 seconds to see my husband’s face, and when I think back now, he wasn’t gasping for air or anything like that. He just looked scared.”

According to Sharon, she was told Jeffrey would be ventilated for three days “just to give his lungs a break.” Yet, “he was on the ventilator for 20 days after that” — until the day he died.

‘They yelled and screamed at me’

According to Sharon, the doctors repeatedly told her that as long as his kidneys weren’t involved, he would be OK. Yet, “as soon as he got on the ventilator, that’s when they said, ‘Oh, his kidneys are struggling.’ And that’s what remdesivir does.”

Jeffrey was placed on CRRT (continuous renal replacement therapy), a slow dialysis machine. This continued until Aug. 11, 2021, when Sharon remembered a doctor called her and said Jeffrey was “tolerating the CRRT really well” and that he would “try a couple different things” and call back.

“He called me back a couple hours later and said, ‘Jeff’s going to code out today,’” Sharon recalled. “I’m like, ‘a couple hours ago he was doing OK.’”

Sharon says she insisted on visiting her husband, but the doctor “fought” her on it, before relenting. When she did visit, hospital staff told her to “look through the glass” at her husband, before finally being allowed into the room “for two minutes.”

“When I came out, they started to pressure me to put a DNR on him, and I said, ‘I’m not putting a DNR on him.’ They kept pressuring me. I said, ‘my son and I are going to talk about it. We’ll call you back.’ We called them back and I said, ‘we’ve decided that we are not going to do that because if we do it then there is no hope,’” she said.

“They yelled and screamed at me on the phone, but I stuck to my guns,” Sharon recalled. “And a couple hours later, they called and said that Jeff had died.”

Blood clot, kidney troubles began after remdesivir administered

Sharon observed several abnormalities during her husband’s hospitalization and also when she reviewed his medical records.

“What I know now is that his D-dimer levels — and I have all the records to back this up — the evidence is that everything was in the normal range.”

She added:

“After the two doses of remdesivir in the hospital in the ER [emergency room], within three hours of being in the ER, that’s when he developed the blood clot. And they noted it. They were aware of it a couple of times. They noted it, but they didn’t do anything about it.

“The day after he had two doses of remdesivir … doctors noted that his D-dimer is now very elevated, which means you have a pulmonary embolism.”

“They did not treat it for two weeks, and they tested five times within that two-week period,” Sharon said, noting that Jeffrey “ended up having six doses of remdesivir.”

Sharon said Jeffrey was also administered a monoclonal antibody, “one dose to the tune of $27,000,” even though “it was already too late for that — you need to have that in the beginning. This was already 10 days in.”

Ultimately though, for Sharon, her husband’s fate rested on the lack of treatment for his blood clot.

“That’s where it started,” she said. “If they would have treated that blood clot on day one — because people have blood clots all the time — it’s something that you can fix … and send him home. But they didn’t choose to do that. It was like they had him and he was a cash cow for them,” she said, referring to the COVID-19 hospital protocols.

The protocols, prescribed by the CDC, are the subject of a white paper, “Follow the Money: Blood Money in U.S. Healthcare,” which found that the U.S. government incentivized hospitals under the CARES Act (Coronavirus Aid, Relief, and Economic Security Act) to administer treatments such as remdesivir to COVID-19 patients.

According to the report, the average per-person incentive in the U.S. for a “complex COVID inpatient” is $292,566. Hospitals received money for each COVID-19 admission, for the use of remdesivir and for placing patients on ventilators.

‘They were making an example’ of the unvaccinated

Sharon said she believes that Jeffrey’s treatment at the hospital was connected to his unvaccinated status.

“The first day that Jeff was there … the doctor called me and the first question she asked [was], ‘Why weren’t you guys vaccinated?’” Sharon recalled. “I said, ‘Well, because we chose not to be. We are healthy. And this vaccine came out awful fast and we didn’t have a good feeling about it.’”

“That is noted in Jeff’s records over and over and over, that he was not vaccinated or I wasn’t. And at the time that he was in the hospital, it was really when the vaccine was really being pushed out. Basically, they were making an example of the people that came in there that were not vaccinated,” Sharon said.

Sharon also noted that, at Mease Countryside Hospital, patients were being admitted with either an “unvaccinated” or “unknown” vaccination status, perhaps to conceal the number of COVID-19 cases among the vaccinated.

“I know that from a number of nurses that are whistleblowers, that have come out and said that there wasn’t a place to put if you were vaccinated,” Sharon said.

Sharon has since become involved with activist groups who have spoken out on behalf of hospital protocol victims, including the FormerFedsGroup Freedom Foundation and the COVID-19 Humanity Betrayal Memory Project (CHBMP), which developed a list of the 25 commonalities shared by most hospital protocol victims.

According to Sharon, “Of those 25, I think there’s two that didn’t happen” to Jeffrey, noting that her requests that ivermectin, hydroxychloroquine and vitamin D were refused, while vitamin C was administered only on the day of Jeffrey’s death.

“When you look through the drug list, you’ll see that that increased intensely as we got right to the end. He didn’t have a fighting chance,” Sharon said.

Sharon encouraged others who have lost a loved one at a hospital to a COVID-19 diagnosis to carefully check their medical records.

“People need to look at the death certificate. If it says ‘COVID,’ you need to get your medical records and have a doctor, have somebody that’s qualified to look at those records and go through them, just like I did. And they’re going to find that it’s probably not what they think. It’s much worse,” Sharon said.

She also encouraged victims and their families to speak out, noting that even a mere conversation with others can make a difference.

“There’s been many people that once you start to talk about it, then they go, ‘wait a minute.’ So, they start to connect the dots that this could have happened to their person,” Sharon said.

She added:

“There’s a couple of reasons why I fight this so much. One, because they took my husband away from me, and he wasn’t sick and he should never have died. But I’m thinking ahead for my children and my grandchildren. If we don’t stand up and fight for this right now and stop this, it’s going to continue, and we can’t have that. They have to be stopped.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 10, 2024 Posted by | Corruption, Deception | , , , | Leave a comment