The Most Revolutionary Act

Uncensored updates on world events, economics, the environment and medicine

The Most Revolutionary Act
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About stuartbramhall

Retired child and adolescent psychiatrist and American expatriate in New Zealand. In 2002, I made the difficult decision to close my 25-year Seattle practice after 15 years of covert FBI harassment. I describe the unrelenting phone harassment, illegal break-ins and six attempts on my life in my 2010 book The Most Revolutionary Act: Memoir of an American Refugee.

COVID Lockdowns and Mask Mandates Returning? I’m Not Buying the Psyop Distraction, and Neither Should You

https://healthimpactnews.com/wp-content/uploads/sites/2/2023/08/Jesse-Watters-blames-Left-on-Mask-Mandates.jpg

by Brian Shilhavy
Editor, Health Impact News

For the past few days a very controlled narrative has been spun and spread throughout the alternative media, and especially among the Right Wing media, both the corporate Right Wing media, such as Fox News, as well as most of the Right Wing alternative media.

That narrative states that COVID lockdowns and mask mandates are returning.

To be sure, the Liberal Left corporate media is doing their part to fuel this narrative, by publishing “news” stories about the return of the dreaded COVID “virus” cases.

It appears that Alex Jones was selected to begin this current news cycle to hype up fear and outrage, by claiming that a TSA whistleblower, who was unnamed, was stating that “FULL Covid Restrictions” were coming in September.

EXCLUSIVE: Biden Admin Preparing to Bring Back FULL Covid Restrictions, Rollout to Begin Mid-September

Whistleblowers from the TSA and Border Patrol have raised the alarm to Infowars that the Biden administration is setting the stage for full Covid lockdowns that will begin with incremental restrictions like masking TSA employees in mid-September.

The first source, a high-level TSA official confirmed and known to Infowars, reached out to Infowars and cited a Tuesday meeting in which TSA managers were told new memorandums & policies were being completed that would reimplement masking, starting with TSA & airport employees as early as mid-September.

The TSA official also said next week they will receive new guidelines on how the policy will escalate: by mid-October, mask-wearing will be required by pilots, flight staff, passengers, and airport patrons.

After hearing from the TSA manager, Infowars reached out to our trusted Border Patrol source who is also a manager. This source confirmed the same directives were being given to Border Patrol.

They were told it was not a matter of “if” but “when” official Covid numbers will go back up and they expect by mid-October a return to forced-masking policies that the Biden administration previously only reluctantly ended after massive pressure.

Both whistleblowers were told this rollout will be in tandem with the new Covid “variant” hysteria that the MSM has been reporting on this week. (Full article.)

I chose not to report this “news” because it was 100% dependent upon the credibility of Alex Jones, a controversial person, to say the least, in both the alternative and corporate media.

Even if Alex Jones was 100% sincere in what he was reporting, how do we know that this alleged “TSA whistleblower” was not fed this information for the very specific intention of creating a new news cycle around COVID that promoted hype and fear?

It wouldn’t be the first time that agencies like the CIA used the platform of Alex Jones to do something like this, and it probably won’t be the last time.

The other thing that made me skeptical of this “news” by Alex Jones, was that it completely blamed Biden, who is simply a puppet that follows a script (as well as he can in his demented condition) that is written by the corporate Globalists who control these narratives, and control BOTH the Left and Right politicians.

Let’s PLEASE not forget how the first psyop went down with COVID!

It was Donald Trump, the Right-wing Republican President who got all this started, and as the Scamdemic psyop unrolled, ALL politicians, both on the Right and on the Left, supported ALL the emergency health orders, including masks, lockdowns, and COVID vaccines in the beginning.

The entire country, and in fact the entire world, was UNITED around the COVID scam, with very few of us calling these people out and seeing what was happening from the very beginning.

It was only many months later, mostly after the majority of the COVID shots were injected into the arms of millions of Americans, including babies and children, that some of the Right began to voice some opposition to the COVID shots, and most of that opposition was around MANDATES, but not the actual killer shots themselves.

By way of reminder, here is a video I produced that clearly shows that ALL the Republican leaders were on board with the COVID shots as they were being rolled out, and most of them were investing in the new, experimental COVID pharmaceutical products that never would have made it to market without the scare of a “pandemic” and emergency-use orders to put them into the public without proper testing, as unsuspecting victims served as guinea pigs for these new drugs and vaccines.

This is on our Bitchute Channel.

To be able to repeat the 2020-2021 military operation that locked people down, required face masks, and injected as many Americans with a bioweapon shot as possible, is no longer a possible operation, as the country is now divided on these issues, and there is no way the Conservative Right will support a return to these measures, even though they did the first time around.

And then I got further confirmation that this was all a carefully written script to create more hype and fear, when a U.S. Senator actually put out a tweet agreeing with Alex Jones’ “news” about mandates returning, and stated “Over my lifeless body“.

When is the last time you saw a national politician actually make a public statement agreeing with Alex Jones??

Via https://healthimpactnews.com/2023/covid-lockdowns-and-mask-mandates-returning-im-not-buying-the-psyop-distraction-and-neither-should-you/

1971: Bangladesh Declares Independence from Pakistan

Episode 33 Independent Bangladesh

A History of India

Michael Fisher (2016)

Film Review

Bangladesh is the eighth most populated country in the world. Geographically the size of Iowa, its population is half that of the US. Agriculturally rich thanks to alluvial soils deposited by the river Ganges, it’s plagued with immense poverty, corrupt and inefficient government and rising sea levels.

Prior to British occupation, the region had a long history of silk and cotton weaving,* and most early European settlements rose up along Bengal’s early trade networks. Calcutta, which became the center of India’s expanding British economy, was the second largest metropolis in the British Empire (second only to London). For decades, the city was home to the main nationalist networks fighting for Indian independence.

As a direct result of independence, there was a steady transfer of wealth from East to West Pakistan. The former contributed only a tiny minority of  officers and officials to Pakistan’s army and civil service.

The Awami League

In 1953, East Pakistan activists formed the Awami league, whose leaders were imprisoned and whose protests were violently suppressed by Pakistani police. Sheikh Majibar Rahman, who was also active in the Bengali language movement,** was one of the most prominent campaigners for increased East Pakistani autonomy.

In 1971, tensions between East and West Pakistan came to a head following Pakistan’s first fully democratic election. Owing to its far larger population, the Awami League won a majority of seats in Pakistan’s new National Assembly. Pakistan’s military dictator General Yahya Khan responded by dismissing the National Assembly and dispatching the army to “restore order” in East Pakistan.

With the help of the Indian army; the Razakars, an East Pakistan paramilitary force; and the Mukti Bahini, guerilla force India organized from East Pakistani refugees, Bengali nationalists prevailed and established Bangladesh as a sovereign country.

A Stormy Electoral History

Rahman, who advocated a program of “secular socialism and land redistribution, was ineffective in implementing these reforms, in large part due to the 1973-74 famine. His move to consolidate power by making Bangladesh a one party state led to a 1975 military coup and the assassination of Rahman and most of his family.

His daughter Begun Sheikh Hasena, who was away from home, inherited the leadership of the Awami League. She was elected prime minister three times, prior to the military coup by General Ziaur Rahman. After organizing the Bangladesh National Party, he was formally elected president in 1978. Following his 1981 assassination by rival military officers, his widow would be elected twice. A military coup launched by General Hussain Muham Mal Ershad removed her from office in 1983. Ershad subsequently formed the Jatiya Party and won the (likely fraudulent) election in 1986 and 1987. Forced to resign in 1990, Ershad was tried and convicted for corruption.

After he supported the election of Rahman’s widow Khaleda Zia as prime minister in 1991, heavy street protests forced her to appoint a caretaker government to run the 1996 election. This resulted in resulted in Begun Sheikh Hasena’s reelection. Khaleda Zia would replace her in the 2001 election.

Heavy street protests resulted in another military coup in 2007 and the appointment of World Bank economist Fakhruddin Ahmed as martial law administrator. Following major electoral reforms, Begun Sheikh Hasena was reelected in 2008 and 2014 (mainly due to a boycott by the opposition parities).


*The British destroyed East Bengal’s early textile London through large exports of raw India cotton, followed by large imports of cheap industrially woven cotton.

**From the outset, West Pakistani leaders tried to force East Pakistan to adopt Urdu (a Persianized Hindustani language), instead of Bangali, as their official language. Although Bengali and Urdu both evolved from Sanskrit, they are mutually incomprehensible.

Film can be viewed free with a library card on Kanopy.

https://www.kanopy.com/en/pukeariki/watch/video/366254/366237

‘Megalomaniac Ambition for Total Control’: Governments Eye New Gates-Funded Biometric Digital ID System

The Modular Open Source Identity Platform, modeled after India’s biometric database, is expanding globally despite controversy over consent and data protections, but privacy advocates warn the Gates Foundation-funded digital ID initiative could enable tracking citizens “from cradle to grave.”

Spurred in part by the COVID-19 pandemic and the push for digital vaccine “passports,” a growing number of global governments are considering implementing biometric digital ID programs that would require citizens to obtain digital identification credentials to access public goods and services.

Until recently, concerns about the global interoperability of digital systems and the risk of technological “lock-in” to platforms developed by private actors stymied governments’ plans to implement such programs.

Now, backers of a new open-source platform called MOSIP (Modular Open Source Identity Platform) — whose funders include the Bill & Melinda Gates Foundation, the World Bank and eBay founder Pierre Omidyar — are touting the platform as a solution to both these obstacles.

Developed at the International Institute of Information Technology Bangalore in India and modeled after Aadhaar, India’s nationwide digital ID platform and the largest such system in the world, MOSIP “enables countries with low IT capacity to quickly roll out specialized digital identity solutions to their citizens,” according to Identity Review.

Proponents argue the rollout of platforms like MOSIP will help people, especially in low- and middle-income countries, gain access to vital public goods and services.

They also argue the platforms will help the global community fulfill the United Nation’s (U.N.) Sustainable Development Goals (SDGs), which include requiring everyone — including infants — to have a digital identity by 2030 in order to work, vote, and access financial, social and medical services.

But for critics, technologies like MOSIP represent a threat to individual liberty and another step toward a digital panopticon — a widespread rollout of government-mandated surveillance technologies, including “vaccine passports” and other digital identification tools, that spell the end of personal privacy.

What is digital identity?

[…]

Greg Glaser, a California attorney, said, “normal” people think of IDs as a normal thing, but the reality of the biometric digital ID is “far more sinister.”

Glaser said that today, rights, citizenship status, affiliations, standing in court, accounts, privileges, services, land title and more all fundamentally depend on some form of identification.

[…]

Biometric surveillance covers a range of identification measures and technologies, including facial recognition, voice recognition, fingerprint databases, DNA databases, iris scans, heart rate scans, gait recognition — even emotion detection through the analysis of facial expressions and mannerisms.

​According to the Gates Foundation, “Digital ID systems are one of the three pillars of what’s known as digital public infrastructure (DPI)” along with digital payment systems and data exchange systems. They are similar to “the roads and bridges that helped reshape economies in the 19th century.”

“Researchers say DPI can help low- and middle-income countries leapfrog traditional stages of development, lift millions out of poverty, and spur economic growth,” the foundation said.

Such a system “is critical because people need a verified identity in order to tap into DPI’s other benefits, from digital bank accounts and instant payments to mobile phone accounts and personal data management,” said the Gates Foundation.

“If a person cannot prove who they are, how can they take advantage of all of the opportunities society has to offer?” the foundation asked.

According to the foundation, “850 million people around the world … lack any acceptable form of legal identity” and “more than half of those without proof of identity are children whose births were not registered.” One in two women in low-income countries do not have ID, the foundation said.

[…]

MOSIP is aligned with several of the U.N.’s SDGs, including Target 16.9, which calls for the provision of a digital legal identity for all — including newborns — by 2030.

While some claim MOSIP “has been built as a digital public good,” for privacy advocates, the realities of such technologies do not reflect the rosy rhetoric.

Aadhaar, for instance, has already been marked by repeated concerns about its privacy and data protection.

W. Scott McCollough, an Austin-based internet and telecommunications lawyer, told The Defender, “I do not view a mandate to prove my identity as a prerequisite to exercising basic liberties … as anything close to a ‘digital public good.’”

[…]

McCollough also said he’s wary of Gates’ involvement, describing MOSIP as “merely the latest Gates-funded mechanism to total population control. Digital ID, biometrics, CBDC all integrated into an “open” app (powered by a series of APIs) that offers the illusion of autonomy when it is instead the surrender of all self-determinacy to the digital masters.”

[…]

Current rollout of MOSIP

According to the Gates Foundation, 11 countries — nine in Africa and two in Asia — “have signed memoranda of understanding with MOSIP to pilot the system,” adding that “More than 90 million people have been registered for MOSIP-based IDs in the Philippines, Ethiopia, and Morocco as part of national deployments.”

The Hindu reported that other countries using the technology include Burkina Faso, The Republic of Guinea, Sierra Leone, Sri Lanka, the Togolese Republic and Uganda.

In The Philippines, “Around 70 million citizens” — 80% of the population — have enrolled, The Hindu reported, while according to The Economist, Morocco integrated an existing fingerprint database into its national MOSIP platform.

MOSIP relies on biometric data to function. The Gates Foundation cited an example from Ethiopia, “where few people had ever had their fingerprints scanned.” As a result, and “To maximize inclusivity, the team gave people several options for sharing their biometric data, including scans of their fingerprints, iris, or face.”

Iris scanners also were implemented in Sri Lanka and the Philippines as part of MOSIP deployments there, while in June, fingerprint scanners produced by Integrated Biometrics completed the compliance of their scanners with MOSIP for Android devices. This added to existing compliance with Microsoft Windows.

MOSIP supported by Gates Foundation, World Bank, World Economic Forum

The Gates Foundation lauds MOSIP for its academic rather than profit-driven roots and for collaborating with global institutes like the Alan Turing Institute and Carnegie Mellon University.

Yet even without explicit corporate backing, MOSIP has received funding and support from several heavyweight organizations. The Gates Foundation, for instance, issued a $7.27 million grant to MOSIP in September 2018, and a $10 million grant in October 2021.

[…]

Eileen Donahoe, a member of MOSIP’s international advisory group, is executive director of the Global Digital Policy Incubator at Stanford University’s Cyber Policy Center, and a member of the World Economic Forum (WEF), the Council on Foreign Relations and the National Endowment for Democracy.

ID2020, founded in 2016, claims to support “ethical, privacy-protecting approaches to digital ID.” Its founding partners include Microsoft, the Gates Foundation, the Rockefeller Foundation, Gavi, the Vaccine Alliance, UNICEF, and the World Bank.

The Good Health Pass Collaborative — a vaccine passport collaboration also involving Mastercard and the WEF — was also supported by ID2020.

India’s government is also involved with the development of MOSIP. According to The Economist, this is part of Indian President Narendra Modi’s objective to turn his country’s digital public infrastructure into “an Indian Belt and Road Initiative,” through which “Indian IT firms can expect bumper development and maintenance contracts.”

MOSIP in May announced it is building an “ecosystem” of biometrics labs, for which it is “partnering with more universities.”

The Tony Blair Institute, chaired by embattled former U.K. Prime Minister Tony Blair, has also endorsed MOSIP and other digital ID programs. The same institute previously supported ID2020’s Good Health Pass initiative.

People ‘risk being shut out of society’ — unless we opt out

MOSIP’s developers promise “security and privacy features that will help protect the data from potential threats.” According to the company, a “consent framework in the platform takes care of user privacy that lets users choose what they want to share and when.”

Other proponents of digital ID have also argued such platforms allow users to have control over their own data in what is called “self-sovereign identity.”

But McCollough said, “Self-sovereign identity is an illusion since your ‘identity’ has validity or ‘currency,’ only after it is recognized by the government to which we are subject.”

Otherwise, individuals risk being shut out of society, McCollough said. “A person that refuses to grant digital permission soon becomes effectively canceled. Just as there was no spoon in the Matrix there is no self-sovereignty to any of this. They pretend to give you control when the next step is a demand you yield ‘permission’ or else.”

Indeed, Aadhaar, the nationwide Indian digital ID system after which MOSIP is modeled, has been beset by privacy-related controversies.

Launched in 2009, Aadhaar eventually enrolled over 99% of all Indian adults, linking them with many public and private services, including bank accounts, electoral identity verification, income tax filings, digital payments systems, government pensions, subsidies and welfare payments — even SIM card registration.

Yet in 2017, Aadhaar generated controversy when HIV patients reported being coerced into providing their Aadhaar ID, leading many to drop out of treatment programs due to privacy concerns.

According to The Economist, “Aadhaar has performed poorly in places with bad internet connections or where manual workers have worn finger pads. The system also suffers security breaches. Experts say it is very easy to access it with false credentials or spoof fingerprints.”

Nevertheless, Gates, on his personal blog, praised Aadhaar — describing it as “a valuable platform for delivering social welfare programs and other government services.”

[…]

Via https://childrenshealthdefense.org/defender/gates-funded-biometric-digital-id-system/?utm_id=20230823

Dr Andrew Wakefield Was Right All Along

Dr Tess Lawrie

Last month I received an email from Mrs Bridget Wakefield, Dr Andrew Wakefield’s mother. It turned out she lives in Bath, my hometown, birthplace of a Better Way and just a stone’s throw from the World Council for Health offices! She asked whether we could meet.

[…]

What was Dr Andrew Wakefield’s “crime”?

In 1998 Dr Andrew Wakefield, a Fellow of the Royal College of Surgeons and a senior researcher in the University Departments of Medicine and Histopathology at the Royal Free Hospital and School of Medicine published a paper in the Lancet with his colleagues entitled: Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children.

Dr Wakefield’s special interest was inflammatory bowel disease and this paper reported a case series of 12 children with developmental disorders whose mothers also described a constellation of bowel symptoms appearing shortly after their child’s vaccination.

Wakefield’s co-authors included specialist physicians in psychiatry, histopathology, radiology and gastroenterology. After carefully documenting their research findings in the paper, the investigators cautiously concluded: “We have identified a chronic enterocolitis in children that may be related to neuropsychiatric dysfunction. In most cases, onset of symptoms was after measles, mumps, and rubella immunisation. Further investigations are needed to examine this syndrome and it’s possible relation to this vaccine.”

As a medical researcher reading the paper for the first time, without all the accompanying hubris of 1998, I can assure you that the conclusions of this expert group were entirely appropriate: more research was indeed needed. Words like “may” and “possible” suggested a high level of uncertainty among the researchers about a causal link. At a subsequent press conference, Wakefield suggested that it may be prudent to use single vaccines instead of the MMR triple vaccine until this could be ruled out, which sounds like common sense to me as both a doctor and a mother.

[…]

I now wish I had paid attention to Dr Wakefield’s concerns at the time I was raising my young family, as both developmental issues and inflammatory bowel disease are conditions manifest among my children and those of my peers today. Like autism, the prevalence of Crohn’s disease and ulcerative colitis has sky-rocketed in the last 30 to 40 years with little attention paid by health authorities as to the cause/s of this phenomenon.

University professors among other scientists have since published studies that show that childhood vaccination schedules are associated with serious health effects that continue to be ignored by drug regulatory agencies and pharmacovigilance bodies worldwide. In addition, research studies presenting evidence that questions the safety of the childhood vaccination schedule, such as this 2021 paper by Lyons-Weiler and Thomas, continue to be targeted for retraction. In 2020/21 Professor Brian Hooker and Dr Neil Miller conducted a study comparing the health of vaccinated versus unvaccinated children and found developmental delays, asthma, gastrointestinal disorders and ear infections significantly higher among vaccinated children. I’ve had difficulty accessing their 2021 paper entitled “Health Effects in Vaccinated versus Unvaccinated Children” published in the Journal of Translational Science. Perhaps the doi link will work for you 10.15761/JTS.1000459?

In any event, a book detailing the strong case against childhood vaccination is to be published soon and I shall alert you to it when it is. Be prepared for a barrage of fearful and polarising “anti-vaxxer” propaganda in the press.

So why was Dr Andrew Wakefield vilified?

At the time of the Wakefield study, the UK government had just produced a plan to roll out MMR vaccines to all under-fives around the country. Andrew asked them to hold it back until safety could be assured but was told it was not possible.

According to Mrs Wakefield’s, a freelance Sunday Times reporter by the name of Brian Deer launched an attack on Andrew with such voracity that it was “as if he had been told to destroy the man who was going to upset the vaccine programme”. Amazingly, Deer is still on Andrew’s case having published a book as recently as 2020 about his award-winning investigation that destroyed a doctor’s career. The book is called ‘The doctor who fooled the world’ and is published by John Hopkins Press, the university known for the Covid Vaccine Tracker and other Covid activities.

What curious timing indeed that Deer’s book should come out in the year Covid vaccines were launched. Was this to make sure we all know what happens when the bearers of the mighty pen and power of corporate media declare vaccine-concerned doctors to be “‘anti-vaxxers”?

[…]

How to keep ethical doctors quiet

The corporate media’s demonisation of Dr Andrew Wakefield was relentless and continues today. Andrew’s professional hearing went on for three years and, with the medical council desperate to find him guilty of something, he was eventually found guilty of a “callous disregard for children”.

However, parents of allegedly callously disregarded children totally disagreed and tried to set the record straight. They wrote the letter below which concludes with the sentence “We are appalled that these doctors have been the subject of this protracted enquiry in the absence of any complaint from any parent about any of the children who were reported in the Lancet paper.”

Another letter of support from parents can be found in the supplementary material. The latter is from parents who felt misled by a journalist pretending to help their vaccine-damaged child when the motive for engagement was subsequently revealed to be that of making a documentary to discredit Dr Wakefield. “We would like to make it known that we were tricked into appearing”, the letter says.

Scientific Consensus?

It is incredible that it took 12 years for the paper to be retracted. (In Covid times, this can be a matter of days.) On the Lancet paper, Wikipedia erroneously asserts that “The scientific consensus on vaccines and autism is that there is no causal connection between MMR, or any other vaccine, and autism.” and if you visit the Wiki pages you will see the same old names pop up: e.g. vaccinologist Peter Hotez.

To be clear, there is no scientific consensus on this. As with the covid vaccines, open scientific debate and independent scientific evaluation of the effectiveness and safety of the variety of childhood vaccines never happened.

Now that we have heard that the corrupt Dr Anthony Fauci “[is] the science”, we owe it to ourselves and our children to critically rethink our unquestioning embrace of this barbaric voodoo approach to child “health”. Isn’t this what sticking needles into babies is after all?

Like you, it’s the Covid ‘vaccines’ that woke me up…

What Covid has demonstrated is that the pharmaceutical industry is amoral and corrupt, thriving on our disease and not our good health. It will lie and cheat to make billions at our expense and make us sick to ensure lifelong dependency on its chemicals if it can.

In 2010 the medical council finally ruled that Dr Andrew Wakefield was dishonest and the Lancet retracted the paper. Andrew lost his licence to practice and was demonised henceforth as being ‘anti-vax’ – a term thoroughly exploited during the roll out of the inadequately tested and novel covid-19 vaccines religiously given to two-thirds of humanity in the name of The Science.

I have empathy for Andrew and, now that I know what I know about the power and corruption of the vaccine industry, I seriously doubt that he was guilty of the fraud alleged in Wikipedia. Wikipedia alleges many false things these days and can no longer be considered a trustworthy source. Its founder recently revealed that it is run by the CIA, so it would seem to be part of the agenda to brainwash us with a narrative that makes us compliant and fearful.

On the ‘anti-vax’ issue, I too have recently been labelled ‘anti-vax’ by the corporate media, but a more appropriate term is health revolutionary. A revolutionary approach to health and a re-evaluation of vaccines is long overdue!

Whilst the General Medical Council has revealed its true corporate colours during Covid-19, the fact of the matter is that it has been investigating and persecuting doctors who put their patients first for decades. Like Andrew Wakefield, Dr Jayne Donegan is currently enduring a GMC tribunal after firmly sticking to her conviction that “no doctor can ethically deny that children suffer ‘serious, life-changing adverse reactions’ to vaccines”. In addition, there is a list of other doctors who do not agree with the government’s dangerous covid policies who are being “investigated”. I too have been investigated by the medical council on a spurious claim that they could not pursue. No doubt they have dossiers on all who have upheld their Hippocratic Oath during Covid, to do no harm and not give poison to anyone.

[…]

Via https://substack.com/@drtesslawrie

Why Won’t the US Close Guantanamo?

Middle East Eye

Last month, the US Senate passed the National Defence Authorisation Act (NDAA) for 2024, an appropriations bill defining military priorities, and one that has consistently placed restrictions on remedies to the abuses at Guantanamo Bay.

This year’s bill, like many years prior, includes a prohibition on funds to close the infamous prison camp; a prohibition on funds to transfer the incarcerated men out of the prison; a prohibition on the transfer of detainees to Afghanistan, Libya, Somalia, Syria, Yemen and the US; and a prohibition on modifying the prison.

By supporting these measures, federal lawmakers have once again voted to perpetuate the problem of Guantanamo, the violence it is notorious for, and the collective responsibility of the Muslim men detained who have been rendered guilty until proven innocent.

Despite stated opposition from the White House, a veto of the bill seems unlikely.

President Joe Biden, who has made past promises of closing the prison, has taken no action to initiate this process. Rather, he reportedly invested millions of dollars last year in renovating parts of the facility and upgrading its courtroom in a move that The New York Times described as a “retreat from transparency in the already secretive national security cases at the base”.

For the 22nd year, the abuses and lack of accountability at Guantanamo have been codified with no end in sight.

But while the annual passage of the NDAA and its signing by successive presidents have maintained the status quo on Guantanamo, budgetary considerations are far from being the only reason that the forever prison is still in operation and why impunity has reigned.

Ongoing cruelty

This month marks 21 years since the infamous torture memos were drafted and signed by the US Office of Legal Counsel, effectively sanctioning the use of torture and allowing the US to unabashedly and openly conduct war crimes.

According to one memo, in order for the physical infliction of pain to be considered torture, it would have to be “equivalent in intensity to the pain accompanying serious physical injury, such as organ failure, impairment of bodily function or even death”.

After the memos were released, former President Barack Obama made sure to announce that no one would be prosecuted for these crimes and would go on to casually remark some years later that “we tortured some folks“.

Yet the effects of that torture, including confessions made under duress and extreme violence, continue to render the remaining prisoners at Guantanamo guilty and perpetuate their ongoing suffering. Obama’s inaction undoubtedly set a precedent of impunity – one that would be justified over and over again.

Mere weeks before US senators voted the NDAA into law, the UN published a report on the abuses at Guantanamo Bay by the special rapporteur on human rights and counter-terrorism, Fionnuala Ni Aolain. Ni Aolain was the first independent UN investigator to visit the facility in its nearly 22 years of operation.

The 23-page report, which renewed the global spotlight on Guantanamo, is a scathing critique of the government’s treatment of current and former detainees and a thorough indictment of the US government’s systematic crimes of extraordinary rendition, arbitrary detention, and deliberate and extensive mechanisms to deny individuals their rights.

“Several US government procedures establish a structural deprivation and non-fulfilment of rights necessary for a humane and dignified existence and constitute at a minimum, cruel, inhuman and degrading treatment across all detention practices at Guantanamo Bay,” the special rapporteur writes.

With just 30 remaining out of the nearly 800 prisoners the detention centre once held, Ni Aolain is also careful to address post-Guantanamo life for former prisoners, and how their conditions maintain the prison’s cruelty. “For many former detainees, their current experience in their home or third country merely becomes an extension of arbitrary detention in Guantanamo, with some even expressing that they wish to return,” the report states.

But renewed attention on the crimes at Guantanamo has also meant renewed denials by the US government. Despite the formal critiques, American officials blithely dismissed the special rapporteur’s detailed review in a generic response that could have just as easily been written before her visit.

Thoroughly consistent with all its efforts to deny the violence at Guantanamo, the US’s reply was not just a categorical rejection of the report, but a powerful symbolic refusal – at the highest levels – to pursue any remedies, let alone any semblance of accountability, for its victims.

To this end, the US insisted that it disagreed “in significant respects with many factual and legal assertions”, and that it was “committed to providing safe and humane treatment for detainees at Guantanamo, in full accordance with international and US domestic law”.

Despite testimony by countless former prisoners and even former guards at Guantanamo and CIA black sites, the US government continues to double down on its assertions, demonstrating that no individual, human rights organisation or institutional body – much less one without actual authority over the US – could move the US to respond any differently.

Nevertheless, the US stated that it would be “carefully reviewing” the recommendations and “will take any appropriate actions, as warranted”.

What would actually warrant a change though? The US has been continuously condemned for its operations and treatment of those incarcerated to no avail.

In fact, over the last 13 years, the US has been subjected to three evaluations of its human rights records under the Universal Periodic Review process. Every one of the reports repeatedly called attention to the abusive conditions at Guantanamo and urged its immediate closure. And for every official criticism, the US government issued a response denying allegations of inhumane treatment while justifying its policies at Guantanamo and lack of action.

Not only did the brutality continue under Obama, but since 2010, the restrictions in the NDAA, especially in blocking funds to release and transfer Guantanamo detainees, have increased. Obama, like every other president, elected not to veto the bill.

Facade of accountability

Although the US finally allowed a UN torture investigator’s visit to Guantanamo without restrictions, it was not to invite accountability. It was instead to promote the facade of accountability after 22 years by allowing the visit in the first place – only to categorically reject any wrongdoing. In other words, the US is not committed to accountability but to the creation of contested narratives that have long outlived the truth. Government impunity, after all, was built into the War on Terr0r’s legal infrastructure.

It is telling that, in the wake of a UN report on Guantanamo, US lawmakers would pass the NDAA once more with bipartisan support and seemingly no debate either on Capitol Hill or in the media about the provisions related to the detention centre. For years, US lawmakers proudly boasted about prolonging the torture at Guantanamo, but now there doesn’t even seem to be a need to address what has become an inevitability.

If the last 20 years have taught us anything, it is that there has never been, nor is there likely ever to be, any accountability for this disastrous and deeply Islamophobic project that has no conceivable end.

[…]

Via https://www.middleeasteye.net/opinion/guantanamo-why-us-not-close

Tens of Thousands of Mothers Sue Makers of Tylenol for Pregnancy Use that Led to Babies Born with Autism

by Brian Shilhavy
Editor, Health Impact News

Tens of thousands of mothers are suing the makers of Tylenol for using the popular over-the-counter pain reliever during pregnancy, which resulted in them giving birth to babies diagnosed with autism.

Tens of thousands of mothers are suing the makers of Tylenol in a class-action lawsuit that claims its use during pregnancy led babies to be born with autism.

A study from the NIH found that pregnancy exposure to acetaminophen, the main ingredient in Tylenol, may increase a child’s risk for autism and ADHD.

Karleen DeGroodt is among the mothers in the lawsuit and discussed her use of Tylenol during pregnancy and her son’s autism during an appearance on NewsNation’s “Prime.” (Full article.)

Last October, a federal judicial panel consolidated dozens of these lawsuits alleging that acetaminophen, the active ingredient in Tylenol and generic versions of the drug, can cause autism spectrum disorder and attention deficit hyperactivity disorder.

TorHoerman Law is one of the law firms representing these mothers, and they have produced the following video explaining the lawsuit.

[The main defendant in the lawsuit is Kenvue, which is the former Johnson & Johnson’s consumer health unit that is now a “spin-off” of J&J. (Source)

Co-defendants in the lawsuit are CVS Health, Rite Aid Corp, Safeway Inc, Target Corp and Walgreens Boots Alliance, which are being charged with failing to warn consumers about the risks of Tylenol.

Kenvue has suffered some setbacks in recent weeks in trying to get some of the lawsuits dismissed, with one of the reasons given to dismiss the lawsuits being that the FDA had approved the product and its labels.

Kenvue Inc cannot immediately appeal a federal judge’s order allowing lawsuits claiming that its popular over-the-counter painkiller Tylenol can cause autism in children of mothers who take it during pregnancy, the judge has ruled.

U.S. District Judge Denise Cote in Manhattan on Thursday ruled that Kenvue, formerly Johnson & Johnson’s consumer health unit, had not shown any basis for allowing the unusual step of an appeal to the 2nd U.S. Circuit Court of Appeals before final judgment in the case.

In April, Cote denied Kenvue’s motion to dismiss one of the lawsuits on the grounds that the U.S. Food and Drug Administration’s approval of Tylenol’s label preempted any state law claims. Had she ruled in the company’s favor, it would have ended the entire litigation. (Source.)

The amount of studies published in the medical journals linking Tylenol taken during pregnancy to babies born with autism is overwhelming.

Here are just a couple of the more recent studies published this year (2023).

Acetaminophen causes neurodevelopmental injury in susceptible babies and children: no valid rationale for controversy

Clinical and Experimental Pediatrics – June 14, 2023

Abstract

Despite worldwide acceptance of acetaminophen as a necessary medicine in the field of pediatrics, evidence that early life exposure to acetaminophen causes neurodevelopmental injury in susceptible babies and children has mounted for more than a decade.

Evidence is diverse, including extensive work with laboratory animals, otherwise unexplained associations, factors associated with the metabolism of acetaminophen, and some limited studies in humans. Although evidence has reached an overwhelming level and has been reviewed in detail recently, some controversy remains. In this narrative review, some of those controversies are evaluated.

Evidence from the prepartum and the postpartum period is considered, avoiding controversies raised by considering only the limited evidence pointing exclusively toward risks during the prepartum period. Among other issues, the associations through time between acetaminophen use and the prevalence of neurodevelopmental disorders are considered.

A systematic review reveals that the use of acetaminophen in the pediatric population was never tracked carefully, but historical events that affected use of the drug were documented and are sufficient to establish apparent correlations with changes in the prevalence of neurodevelopmental disorders.

In addition, problems with exclusive reliance on results from meta-analyses of large datasets and from studies involving small time frames of drug exposure are reviewed. Further, evidence demonstrating why some children are susceptible to acetaminophen-induced neurodevelopmental injury is examined.

It is concluded that, at least among the factors considered, there is no valid rationale for controversy regarding the conclusion that early life exposure to acetaminophen causes neurodevelopmental injury in susceptible babies and small children. (Source.)

The use of acetaminophen in pregnancy: a double whammy

Annals of Medicine and Surgery – March 14, 2023

Abstract

Acetaminophen is the most widely over the counter used analgesic in the world, and the World Health Organization advises using it as first-line treatment for pain issues (WHO).

However, various side effects have been documented with its use such as nausea, vomiting, constipation at low doses whereas in large doses, it might even result in hepatoxicity.

Recent literature suggests that the use of acetaminophen in pregnancy even in optimal doses could result infant being born with ADHD and autism, so in this short communication we talk about the prevalence of neurodevelopment disorders in infants as a result of its use, as well as shed light to the measures that should be adopted to minimize the adverse effects. (Source.)

We have been publishing articles exposing the dangers of Tylenol for over a decade now. A search on Health Impact News for this killer drug, which is available as an over-the-counter (OTC) drug that even minors can purchase in their local pharmacy or retail store will result in over 80 articles.

Pregnant women are the not the only ones who should immediately STOP using this killer drug. NOBODY should be using it.

Tylenol is a classic example of how corporate profits from the pharmaceutical drug companies are far more important than patient safety, as millions of lives are sacrificed to keep these drugs on the market.

It is also just another example of how the FDA works to protect pharmaceutical companies, and NOT consumers.

Tylenol has been on the market for 75 years bringing in annual revenues that exceed $300 million.

And the adverse effects from Tylenol have been widely published for over a decade now.

In 2013 ProPublica published one of the most comprehensive reviews of Tylenol’s toxic side effects:

About 150 Americans a year die by accidentally taking too much acetaminophen, the active ingredient in Tylenol. The toll does not have to be so high.

During the last decade, more than 1,500 Americans died after accidentally taking too much of a drug renowned for its safety: acetaminophen, one of the nation’s most popular pain relievers.

Acetaminophen – the active ingredient in Tylenol – is considered safe when taken at recommended doses. Tens of millions of people use it weekly with no ill effect. But in larger amounts, especially in combination with alcohol, the drug can damage or even destroy the liver.

Davy Baumle, a slender 12-year-old who loved to ride his dirt bike through the woods of southern Illinois, died from acetaminophen poisoning. So did tiny five-month-old Brianna Hutto. So did Marcus Trunk, a strapping 23-year-old construction worker from Philadelphia.

The toll does not have to be so high.

The U.S. Food and Drug Administration has long been aware of studies showing the risks of acetaminophen – in particular, that the margin between the amount that helps and the amount that can cause serious harm is smaller than for other pain relievers. So, too, has McNeil Consumer Healthcare, the unit of Johnson & Johnson that has built Tylenol into a billion-dollar brand and the leader in acetaminophen sales.

Yet federal regulators have delayed or failed to adopt measures designed to reduce deaths and injuries from acetaminophen overdose, which the agency calls a “persistent, important public health problem.”

The FDA has repeatedly deferred decisions on consumer protections even when they were endorsed by the agency’s own advisory committees, records show. (Full article.)

[…]

Via https://healthimpactnews.com/2023/tens-of-thousands-of-mothers-sue-makers-of-tylenol-for-pregnancy-use-that-led-to-babies-born-with-autism/

 

EPA Stymies 6-Year Effort to Limit Water Pollution From Factory Farms

Public health and environmental advocacy groups said that the U.S. Environmental Protection Agency (EPA) chose to benefit the factory farming industry instead of protecting communities and drinking water on Aug. 15 when it denied an anti-pollution petition filed in 2017 by nearly three dozen groups.

Food & Water Watch (FWW), the Center for Food Safety (CFS) and North Carolina Environmental Justice Network were among the organizations that filed the petition six years ago and sued the agency last year due to its “unreasonable delay” in answering the request for stronger rules to prevent water pollution from hundreds of thousands of factory farms across the United States.

The EPA responded to the legal challenge on Aug. 15 by denying the original petition and announcing it would form a federal subcommittee to study the effects of pollution from concentrated animal feeding operations (CAFOs) and make recommendations to the agency.

The subcommittee is expected to convene in 2024 and its work could take 12-18 months, leaving open the possibility that — should President Joe Biden lose his reelection campaign next year — the question of regulating factory farm pollution could be left up to a Republican administration.

 

“Factory farms pose a significant and mounting threat to clean water, largely because EPA’s weak rules have left most of the industry entirely unregulated,” said Tarah Heinzen, legal director for FWW.

Heinzen continued:

“EPA’s deeply flawed response amounts to yet more delay, and completely misses the moment.”

Though the EPA pledged to study the effects of water pollution from factory farms, the petitioners noted that the impact has already been well-documented.

According to the Sierra Club, “water pollution is possible at virtually any point in a CAFO’s operation,” as waste from factory farms is generally not treated for disease-causing pathogens, chemicals, pharmaceuticals or heavy metals.

Animal waste spills and overflows can lead to contaminated runoff that ends up in waterways, stormwater can mix with manure and milkhouse waste that flows into drains, waste storage units can overflow or burst and catch basins can inadvertently drain waste into waterways.

CFS said in a statement that factory farms “operate like sewerless cities” and can contaminate “drinking water with cancer-causing nitrates” as well as flooding homes with waste during storms and leaving communities without safe places for water recreation.

Citing the EPA’s own data in a 2020 brief, FWW found that pollution from factory farms “threatens or impairs over 14,000 miles of rivers and streams and more than 90,000 acres of lakes and ponds nationwide.”

“We know that animal factories are a huge source of water pollution and that our freshwater is in crisis, and yet EPA has failed to uphold its duty to protect our environment from this industry,” said Amy van Saun, a senior attorney with CFS.

Saun continued:

“We have a right to clean and safe water and we cannot afford to wait any longer to stop the tide of pollution from animal factories.”

The 2017 petition called on the EPA to improve the CAFO permitting process, as fewer than one-third of the largest 21,000 factory farms have National Pollutant Discharge Elimination System permits, which regulate the point sources that discharge pollutants into waterways.

Ben Lilliston, director of rural strategies at the Institute for Agriculture and Trade Policy, said that by denying the petition the EPA “chose to further a special exemption for factory farms that benefits global meat companies while undermining independent farmers raising animals in ways that protect our water.”

[…]

Via https://childrenshealthdefense.org/defender/epa-water-pollution-factory-farms-cd/

FDA Shrugs Off Concerns About Premature Births, Approves Pfizer RSV Vaccine for Pregnant Women

By  Brenda Baletti, Ph.D.

The U.S. Food and Drug Administration on Monday approved Pfizer’s Abrysvo vaccine, a maternal vaccine meant to protect infants against respiratory syncytial virus, or RSV, through 6 months of age — despite safety concerns, including from the FDA’s own advisers.

The agency approved the vaccine despite concerns raised by members of the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) about premature births identified during Pfizer’s clinical trials.

VRBPAC panelist Dr. Paul Offit, a pediatrician at Children’s Hospital of Philadelphia and a frequently cited vaccine advocate, said he doesn’t believe there is enough data to indicate the safety of the vaccine is “reassuring.”

In its statement to investors, however, Pfizer was enthusiastic about the prospect of the vaccine.

“ABRYSVO’s approval as the first and only maternal immunization to help protect newborns immediately at birth through six months from RSV marks a significant milestone for the scientific community and for public health,” said Annaliesa Anderson, Ph.D., Pfizer’s senior vice president and chief scientific officer, Vaccine Research and Development.

RSV generally causes only mild, cold-like symptoms in infants and young children, most of whom get the illness by age 2 and typically don’t require medical attention. The Centers for Disease Control and Prevention (CDC) estimates 58,0000-80,0000 children younger than age 5 are hospitalized and 100-300 children die from RSV overall in any given year.

Commenting on the vaccine after VRBPAC endorsed it in May, Dr. Peter McCullough told The Defender:

“This product represents an unprecedented attempt to vaccinate mothers for no benefit to them and only theoretical efficacy in babies. In the trial, less than 2% of infants at any time point contracted RSV, which is easily treatable with nebulizers.”

Before the drug can be prescribed to pregnant women, the CDC’s Advisory Committee on Immunization Practices (ACIP) must recommend the vaccine and CDC Director Mandy Cohen must accept the recommendation. She is widely expected to do so, STAT News reported.

The next ACIP meeting is scheduled for October, but STAT said a special meeting might be called in the coming days, given “last year’s early start to the RSV season.”

Earlier this month, the CDC recommended the first-ever monoclonal antibody — Sanofi and AstraZeneca’s Beyfortus — to protect all newborns against RSV after the FDA approved the drug.

It made that recommendation despite 12 infant deaths during the clinical trials and criticism from medical experts who said the move was unnecessary and not worth the known risks.

In late May, the FDA approved the same Pfizer Abrysvo vaccine approved Monday for pregnant women for use in adults over 60.

And earlier in May the agency approved GSK’s Arexvy, the first vaccine authorized for RSV, for adults over 60.

20% higher rate of premature birth among vaccinated mothers in clinical trials

According to the FDA, Abrysvo will be administered to pregnant women between 32 and 36 weeks of pregnancy as a single-dose injection into the muscle.

It said the “safety and effectiveness” of the shots were determined through “ongoing, randomized, placebo-controlled international clinical studies.”

Pfizer reported that in its Phase 3 clinical trial — MATISSE (MATernal Immunization Study for Safety and Efficacy), published in the New England Journal of Medicine — the shot was nearly 82% effective at preventing severe disease from RSV in newborns during the first 90 days of life. There were about 7,000 participants in the clinical trial.

The vaccine was also reported to be about 70% effective during the first six months of the baby’s life, CNBC reported.

But experts, including four members of the VRBPAC committee who voted against recommending the vaccine for pregnant women, said they had concerns about the study.

Tracy Høeg, M.D., Ph.D., reported there was a 20% higher rate of preterm birth in the vaccinated group than in the unvaccinated group.

“Most of VRBPAC shrugged off the signal as ‘non significant’ but study underpowered,” she tweeted — meaning there were not enough participants in the study to confirm whether the safety signal was statistically significant.

Hoeg shared more details on Twitter

Offit voted against approving the vaccine because of the safety signal.

The FDA, following Monday’s approval, said the available data “are insufficient to establish or exclude a causal relationship between preterm birth” and Pfizer’s vaccine, CNBC reported.

It also reported that Pfizer’s VP of Vaccine Research and Development Alejandra Gurtman said the difference in premature birth rates was “not statistically significant.”

Gurtman noted that most premature births occurred 30 days after vaccination, which she said means “a very close causal relationship between the vaccine and preterm birth couldn’t be identified.”

“We couldn’t find any reason why this really happened,” Gurtman said.

GSK stopped development of the same type of maternal RSV vaccine earlier this year when it detected a similar increase in the number of preterm births among pregnant mothers.

Other commonly reported side effects from Abrysvo included pain at the injection site, headache, muscle pain and nausea.

Pre-eclampsia also occurred in 1.8% of pregnant women who took the drug, relative to 1.4% of women in the placebo group.

The company said it will continue to examine risks in a post-marketing vaccine study, and as part of that, it will create a registry for adverse event reporting.

McCullough wrote on his Substack that this vaccine is more evidence that “Vaccine ideology or hubris appears everywhere! Never had we heard so much about vaccines in our day to day life as laypersons or as healthcare professionals.”

He added:

“Pfizer has aggressively advanced RCTs into the pregnant population with no assurances on long term outcomes. There is no direct benefit to the mothers.

“Furthermore, the sponsors moved the goalposts to make it easier to have a successful trial. We should demand long-term safety, high efficacy … and at least one year of durability, for such a rare and easy-to-treat condition in babies.”

[…]

 

Via https://childrenshealthdefense.org/defender/fda-pfizer-rsv-vaccine-pregnancy/

 

Court Documents Suggest Justice Department Under Four Presidents Covered Up Jeffrey Epstein’s Money Laundering at JPMorgan Chase

JPMorgan Chase BuildingBy Pam Martens and Russ Martens

Wall Street on Parade

:Remember all of that sensational social media buzz in 2016 about a politically-connected ring of pedophiles operating out of a pizza parlor in Washington, D.C.? The story was debunked by Snopes but not before it had gone viral.

While the pizza parlor was getting plenty of attention, an actual, highly sophisticated, child sex-trafficking ring had been operating with impunity for more than a decade out of the largest bank in the United States, JPMorgan Chase.

Based on astonishing internal documents from JPMorgan Chase obtained during discovery in a federal lawsuit and filed on the court docket last week, it now appears that the U.S. Department of Justice has turned a blind eye toward this bank’s facilitation of Jeffrey Epstein’s sex trafficking crimes for more than 16 years, during the administrations of four separate Presidents of the United States.

The heavy-lifting for what should have been a criminal investigation by the U.S. Department of Justice in this matter is now being conducted by the U.S. Attorney’s Office for the U.S. Virgin Islands in a civil lawsuit, using the law firm, MotleyRice.

A new document filed last week with the federal court in Manhattan that is hearing the case shows that on September 6, 2007, the U.S. Attorney’s Office for the Southern District of Florida (part of the U.S. Department of Justice) followed up on a subpoena it had issued to Bear Stearns, demanding to receive “a list of accounts at other financial institutions that Bear Stearns has either transferred money to or received money from on behalf of Mr. Epstein….”

The peculiar thing about this letter is that a federal law enforcement agency is asking a private bank to help it locate Epstein’s other bank accounts when it has that information easily accessible at two federal databases: the Financial Crimes Enforcement Network (FinCEN) and the Federal Reserve System which handles the wiring of funds between banks and others.

In fact, the U.S. Department of Justice has a Financial Investigations Guide that specifically lists those two sources as key government databases to tap when conducting a financial investigation into money laundering or other criminal financial activity.

One reason that comes to mind as to why a federal prosecutor would ask a private bank like Bear Stearns to provide outside banking relationships for Jeffrey Epstein, instead of getting that information directly from reliable government databases, is that the prosecutor didn’t want to know or was instructed by higher ups to stand down.

This is the same U.S. Attorney’s Office in the Southern District of Florida that had received a deeply investigated case from the Palm Beach County Police Department, documenting that Epstein had sexually assaulted dozens of schoolgirls at his Palm Beach home. Under a secret non-prosecution agreement, this same U.S. Attorney’s Office agreed not to prosecute Epstein or his accomplices for federal crimes. Epstein ended up with a lenient 18-month jail sentence in 2008, which morphed into 13 months, the bulk of which was a work release program where Epstein was driven by his limo driver to an office each day.

Because of that abysmal failure by the U.S. Department of Justice, Epstein was able to continue his sexual assaults of underage girls and arrange for his rich pals to do the same, from his release from jail in Palm Beach County in July of 2009 until the Justice Department was shamed by the Miami Herald’s “Perversion of Justice” newspaper series in November of 2018 into arresting Epstein on federal charges of sex trafficking of minors on July 8, 2019. (Epstein was found dead in his jail cell while awaiting trial a little more than a month later, on August 10, 2019. His death came the day after an appellate court released 2,000 pages of previously sealed documents, including the names of politicians and other powerful men that a victim alleged were part of his sex ring. The New York City Medical Examiner ruled that Epstein’s death was a suicide.)

A federal appellate court that looked at the Justice Department’s handling of the Epstein case and its failure to inform his victims’ about its non-prosecution agreement, called it “a national disgrace.”

Throughout this period, the largest taxpayer-backstopped, federally-insured bank in the United States, with media darling Jamie Dimon sitting at its helm, was somehow able to engage in more than 9,000 money transactions for Epstein, which “had a combined value of over $2.4 billion,” according to court evidence introduced by the U.S. Virgin Islands.

Those transactions included the following amounts of hard cash according to documents obtained by the U.S. Virgin Islands:

“In the year 2003, Epstein was able to withdraw highly suspicious amounts of cash totaling $175,311. In 2004, he withdrew $840,000. In 2005, he withdrew $904,337. In 2006, he withdrew $938,625. In 2007, he withdrew $526,000. In 2008, he withdrew $469,000. In 2009, he withdrew $165,011. In 2010, he withdrew $253,397. In 2011, he withdrew $260,000. In 2012, he withdrew $290,000. In 2013, he withdrew $197,152.”

So let this sink in for a moment. The Justice Department’s U.S. Attorney’s Office in the Southern District of Florida was supposedly on a subpoena hunt in September of 2007 to learn the names of any other banks that might be laundering money for Epstein. But, somehow, despite government databases being readily available to provide the name of his most important bank, JPMorgan Chase, Epstein was able to withdraw millions of dollars in hard cash from that bank, unimpeded for years – when any cash withdrawal of $10,000 or more should have blown the whistle on Epstein and stopped his operation.

During the financial crisis in 2008, JPMorgan Chase bought the collapsing Bear Stearns and, apparently, obtained its records. The U.S. Virgin Islands was able to obtain during discovery the internal emails at JPMorgan Chase, where its anti-money-laundering personnel express curiosity as to why Bear Stearns got a subpoena in the Epstein case but it didn’t, despite being Epstein’s primary bank.

In a January 10, 2011 internal email at JPMorgan Chase, Maryanne Ryan, the Vice President of Anti-Money-Laundering (AML) Operations, emails William Langford, then Global Head of Compliance at the bank according to his LinkedIn profile (and a former executive at FinCEN who should have intimately understood the need to be filing Suspicious Activity Reports for Epstein’s massive cash withdrawals).

Ryan reveals the following: that JPMorgan Chase “never was served a subpoena,” which she admits that she finds “odd, since we were his #1 bank and actually Bear got one in 07.” Ryan also reveals in this email that “Steve Cutler” has approved Epstein to remain as a customer at JPMorgan Chase’s Private Bank. Steve (Stephen) Cutler was the former Director of Enforcement at the Securities and Exchange Commission prior to becoming General Counsel at JPMorgan Chase. According to the transcript of the deposition of Jamie Dimon, the Chairman and CEO of the bank, as part of the U.S. Virgin Islands’ lawsuit, Cutler worked in the office directly next door to Dimon and reported to Dimon.

Dimon also stated in his deposition that he had never heard of Epstein and didn’t know he had accounts at the bank until Epstein’s arrest in 2019. It raises much skepticism on Wall Street that Cutler, who reported to Dimon, would have failed to get permission from Dimon before deciding to keep this Level 3 registered sex offender at the bank and look the other way at hundreds of thousands of dollars in cash withdrawals year after year.

For example, another internal email filed with the court shows that on October 24, 2008 an employee writes that it is his understanding that JPMorgan Chase “requires top of the house ok for clients who are convicted felons.” He cites this chain of approval as follows: “PCS Legal [Private Client Services Legal] to Asset Mgt Legal to Cutler to Jaime Daimnon [Jamie Dimon].”

Other internal documents show that Epstein was catered to at the bank because he referred large accounts from ultra wealthy individuals, notwithstanding the fact that the anti-money-laundering personnel at the bank were regularly circulating media reports about Epstein’s scandalous history.

The head of the U.S. Attorney’s Office for the Southern District of Florida at the time Epstein was let off the hook with the secret federal non-prosecution agreement was Alex Acosta. Donald Trump made Acosta the head of the U.S. Department of Labor – a key federal agency in preventing human trafficking. Acosta resigned in 2019 after news reports focused on the secret non-prosecution agreement Acosta has presided over for Epstein in the Palm Beach County case.

The U.S. Department of Justice has failed to bring charges against JPMorgan Chase despite what appears to be a mountain of evidence that it laundered money for Epstein through four different Presidents and their appointees at the U.S. Department of Justice: George W. Bush, Barack Obama, Donald Trump, and Joe Biden.

[…]

Via https://wallstreetonparade.com/2023/08/new-court-documents-suggest-the-justice-department-under-four-presidents-covered-up-jeffrey-epsteins-money-laundering-at-jpmorgan-chase/

Putin Calls on BRICS to Guarantee Food and Energy for the World

Russian President Vladimir Putin, Aug. 22, 2023.

Russian President Vladimir Putin, Aug. 22, 2023. | Photo: X/ @LFCNewsMedia

teleSUR Newsletter

The Russian president reiterated his willingness to send shipments of up to 50,000 tons of grain for free to six African countries.

On Tuesday, Russian President Vladimir Putin called for expanding cooperation among the BRICS countries, which is led by Brazil, Russia, India, China and South Africa.

“Russia is in favor of establishing closer cooperation within the BRICS framework for the reliable and uninterrupted supply of energy and food resources to world markets,” he said during his speech by videoconference at the Economic Leaders Forum, which is held as part of the 15th BRICS Summit in Johannesburg.

Moscow is increasing supplies of fuel, agricultural products and fertilizers to countries in the Global South, Putin said, stressing that this foreign policy seeks to contribute to the fight against poverty and hunger in the countries most in need.

The Russian leader also insisted that his country is capable of replacing Ukrainian grain in the world, either as a commercial product or as part of humanitarian aid endowments.

Reiterating the promise made at the St. Petersburg’s Russia-Africa summit, Putin indicated his willingness to send shipments of up to 50,000 tons of grain for free to six African countries.

“The talks with the partners are already concluding,” he said, noting that Russia has had “a magnificent harvest” this year.

The Russian leader once again insisted that the Kremlin is willing to return to the Black Sea Initiative on grain exports if all its conditions are met.

In this regard, Putin also recalled that the West has put obstacles to Russian grain and fertilizer supplies since the special military operation in Ukraine began 18 months ago.

[…]

Via https://www.telesurenglish.net/news/Putin-Calls-on-BRICS-to-Guarantee-Food-and-Energy-for-the-World-20230822-0015.html