How the Taliban crushed the CIA’s heroin bonanza in Afghanistan
The Taliban has not once, but twice eradicated Afghanistan’s poppy cultivation, the world’s largest source of heroin.
By William Van Wagenen | The Cradle | July 7, 2023
In the aftermath of the chaotic US and UK withdrawal from Afghanistan in August 2021, Pakistani journalist Hamid Mir warned in the Washington Post of the dangers of “ignoring one important consequence of the Taliban takeover: the coming boom in Afghanistan’s narcotics trade.”
Mir then boldly predicted that, “in the next few years, a flood of drugs from Afghanistan may become a bigger threat than terrorism.”
This projection of an international drug trade boom seemed plausible, considering the longstanding accusations that the Taliban funded their two-decade insurgency against the occupying forces by controlling opium production. In fact, it was believed that 95 percent of heroin used in Britain originated from Afghan opium.
It comes as a surprise then, that a June 2023 report published by Alcis, a British-based geographic information services firm, revealed that the Taliban government had all but eliminated opium cultivation in the country, wiping out the base ingredient needed to produce heroin. This outcome mirrored a similar move by the Taliban in 2000 when they were in power the first time.
Ironically, instead of praising Kabul’s new leaders for quashing the source of illicit drugs, the international community responded to this development with criticism. Even the US Institute for Peace (USIP), which is funded by the US government, argued that “The Taliban’s successful opium ban is bad for Afghans and the world.”
Such western displeasure towards the Taliban’s efforts to dismantle the global heroin trade may seem perplexing at first glance.
However, a closer examination of events in Afghanistan reveals a different perspective. Under the guise of the “War on Terror,” the 2001 US and UK invasion was driven in part by the desire to restore the heroin trade, which the Taliban had abruptly terminated just a year earlier.
The western powers sought to reestablish the lucrative flow of billions of dollars that the heroin trade provided to their financial systems. In fact, “For 20 years, America essentially ran a narco-state in Afghanistan.”
‘Dollar for Dollar’
To understand the origins of the Afghan heroin trade, a review of US involvement in the central Asian nation is necessary, beginning in 1979 when the CIA embarked on a covert program to undermine the pro-Soviet Afghan government in Kabul.
The US covertly supported an umbrella of Muslim guerrilla fighters known as mujahideen, with the hope that provoking an insurgency would entice the Soviet Army to intervene. This calculated move would force the Soviets into occupying Afghanistan and engaging in a protracted and costly counter-insurgency campaign, thereby weakening the Soviet Union over time.
To accomplish this, the CIA turned to its close allies, Saudi Arabia and Pakistan, for help. Saudi Prince Bandar bin Sultan facilitated a meeting between CIA Director William Casey and Saudi King Fahd, in which the Saudis committed to matching “America dollar for dollar supporting the mujahedeen.”
The US and Saudi Arabia, with help from Pakistani’s Inter-Services Intelligence (ISI), set up training camps for the mujahideen in Pakistan, and supplied them with advisors, weapons, and cash to fight the Soviets.
Gulbaddin Hekmatyar, the founder of the Hizb-i-Islami militia, was among the most prominent mujahideen leaders, receiving some $600 million in aid from the CIA and its allies.
Journalist Steve Coll writes in his Pulitzer Prize-winning book Ghost Wars that Hekymatyar recruited from the most radical, anti-western, transnational Islamist networks to fight with him, including Osama bin Laden and other Arab volunteers. CIA officers “embraced Hekmatyar as their most dependable and effective ally,” and “the most efficient at killing Soviets.”
Caravans of opium
Aid to Hekymatyar and other mujahideen leaders was not limited to cash and weapons. According to renowned historian Alfred McCoy:
“1979 and 1980, just as the CIA effort was beginning to ramp up, a network of heroin laboratories opened along the Afghan-Pakistan frontier. That region soon became the world’s largest heroin producer.”
The process involved smuggling raw opium gum to Pakistan, where it was processed into heroin in laboratories run by the ISI. The finished product was then discreetly transported via Pakistani airports, ports, or overland routes.
By 1984, Afghan heroin supplied a staggering 60 percent of the US market and 80 percent of the European market, while devastatingly creating 1.3 million heroin addicts in Pakistan, a country previously untouched by the highly-addictive drug.
McCoy states further that, “caravans carrying CIA arms into that region for the resistance often returned to Pakistan loaded down with opium.” Reports from 2001 cited by the New York Times confirmed that this occurred “with the assent of Pakistani or American intelligence officers who supported the resistance.”
In May 1990, the Washington Post reported that the US government had for several years received, but declined to investigate, reports of heroin trafficking by its allies, including “firsthand accounts of heroin smuggling by commanders under Gulbuddin Hekmatyar.”
Rise of the Taliban
When the Soviets did finally withdraw in 1989, the country fell into civil war as the major CIA-backed factions began fighting among themselves for control of the country. Mujahideen leaders became warlords and committed terrible atrocities against the local population while fighting amongst themselves.
It was during this anarchy that religious students from the madrassas (seminary schools), the Taliban, emerged with the help of Pakistani intelligence to take control of the country in 1996, subsequently inheriting the opium trade, which continued unhindered for several years.
In July 2000, however, Taliban leader Mullah Omar ordered a ban on all opium cultivation. Remarkably, the Taliban successfully slashed the opium harvest by 94 percent, reducing yearly production to only 185 metric tons.
Five months later, in December 2000, the US and Russia used the UN Security Council to impose harsh new sanctions on Afghanistan, citing the Taliban’s refusal to hand over Al-Qaeda leader Osama bin Laden following the bombing of the USS Cole in Yemen, in which 17 US sailors were killed. Bin Laden had taken refuge in the Islamic Emirate in 1996 after he was expelled from Sudan.
The New York Times reported that US officials sought to impose the new sanctions, despite warnings from the UN that “a million Afghans could face starvation in coming months because of a drought and continued civil war.”
Following the attacks on 11 September, 2001, Bush administration officials demanded the Taliban hand over Bin Laden once again. Mullah Omar insisted the US first provide evidence of Bin Laden’s guilt, but President Bush refused this request and ordered the US air force to begin bombing Afghanistan on 7 October.
In the wake of the bombing, Mullah Omar dropped the demand for evidence, and offered to hand over Bin Laden to US ally Pakistan for trial. Bush administration officials once again refused.
Journalist and author Scott Horton highlights in his book Fool’s Errand a peculiar aspect of the US campaign: the lack of a clear focus on capturing or eliminating Bin Laden. In fact, President Bush had already stated on 25 September that success or failure should not be defined solely by capturing Bin Laden.
Horton notes further that US planners made no initial effort to hunt down Bin Laden and the foreign Arab fighters supporting him. Instead, head of US Central Command, General Tommy Franks prioritized partnering with Afghan warlord Rashid Dostum to take control of the north of the country, and establish a “land link” to Uzbekistan.
Turning to the warlords
To also capture the capital, Kabul, and other key cities in the south, Alfred McCoy notes the CIA:
“Turned to a group of rising Pashtun warlords along the Pakistan border who had been active as drug smugglers in the south-eastern part of the country. As a result, when the Taliban collapsed, the groundwork had already been laid for the resumption of opium cultivation and the drug trade on a major scale.”
Though US forces were too late to prevent Bin Laden’s escape to Pakistan, the US bombing campaign came just in time for the beginning of poppy planting season. Poppies are planted in the autumn so that the juice from the plant, from which opium is extracted, can be harvested in spring.
McCoy clarified further that, “the Agency (CIA) and its local allies created ideal conditions for reversing the Taliban’s opium ban and reviving the drug traffic. Only weeks after the collapse of the Taliban, officials were reporting an outburst of poppy planting in the heroin-heartlands of Helmand and Nangarhar.”
In December, one of these rising Pashtun warlords, Hamid Karzai, was appointed Chairman of the Afghan Interim Administration and later president.
By the spring of 2002, large amounts of Afghan heroin were once again being transported to Britain via daily flights from Pakistani airports. The Guardian observed the case of a 13-year-old girl who was stopped after she stepped off a Pakistan International Airlines flight from Islamabad to London carrying 13kgs of heroin with a street value of £910,000.
Industrial scale
Thanks to the “land link” established by General Franks, heroin also immediately began flowing north from Mazar-e-Sharif, under CIA ally Rashid Dostum’s control, to Uzbekistan and then to to Russia and Europe.
The flow of heroin was witnessed by Craig Murray, the British Ambassador to Uzbekistan, who explained that Dostum, an ethnic Uzbek, facilitated the smuggling of heroin from Afghanistan to Uzbekistan, where it was then shipped up the railway line, in bales of cotton, to Moscow and then Riga. As Murray noted:
“Opium is converted into heroin on an industrial scale, not in kitchens but in factories. Millions of gallons of the chemicals needed for this process are shipped into Afghanistan by tanker… The four largest players in the heroin business are all senior members of the Afghan government – the government that our soldiers are fighting and dying to protect.”
‘A hands off approach’
In addition to Dostum, Afghan President Hamid Karzai’s younger brother, Ahmed Wali Karzai, quickly secured a prominent role in the Afghan heroin trade.
Credible reports emerged that Wali Karzai was deeply involved in the heroin trade, however, according to the New York Times, the incidents were never investigated, “even though allegations that he has benefited from narcotics trafficking have circulated widely in Afghanistan.”
Senior officials at the US Drug Enforcement Agency (DEA) and the office of the Director of National Intelligence (DNI) complained that the Bush “White House favored a hands-off approach toward Ahmed Wali Karzai because of the political delicacy of the matter.”
The Times later reported that according to a top former Afghan Interior Ministry official, a major source of Wali Karzai’s influence was his control over key bridges crossing the Helmand River on the route between the opium-growing regions of Helmand Province and Kandahar. This allowed Karzai to charge huge fees to drug traffickers to allow their drug-laden trucks to cross the bridges.
Like Dostum and Hekmaytar, Wali Karzai built his heroin empire while on the CIA payroll. The agency began paying Karzai in 2001 to recruit an Afghan paramilitary force that operated at the agency’s direction in and around Kandahar and to rent a large compound for use as the base of the Kandahar Strike Force. The CIA also appreciated Karzai’s help in communicating and sometimes meeting with Afghans loyal to the Taliban.
Karzai also served as the head of Kandahar’s elected provincial council. According to a senior US military officer in Kabul quoted by the Times, “Hundreds of millions of dollars in drug money are flowing through the southern region, and nothing happens in southern Afghanistan without the regional leadership knowing about it.”
The blame game
In late 2004, as reports of Karzai’s involvement in the heroin trade were emerging, Alfred McCoy writes that “the White House was suddenly confronted with troubling CIA intelligence suggesting that the escalating drug trade was fueling a revival of the Taliban.”
A proposal from Secretary of State Colin Powell to fight the heroin trade was resisted by US ambassador to Afghanistan, Zalmay Khalilzad, and then-Afghan finance minister Ashraf Ghani. As a compromise, the Bush administration used private contractors for poppy eradication, an effort that New York Times journalist Carlotta Gall later described as “something of a joke.”
Additionally, reports of a 2005 cable sent by the US embassy in Kabul to Powell’s successor, Secretary of State Condoleezza Rice, viewed Britain as being “substantially responsible” for the failure to eradicate poppy cultivation. British personnel chose where the eradication teams worked, but those areas were often not the main growing areas, and “the British had been unwilling to revise targets.”
The cable also faulted President Karzai, who “has been unwilling to assert strong leadership.” The State Department nevertheless defended him, saying, “President Karzai is a strong partner, and we have confidence in him,” despite reports of his brother’s key role in the heroin trade.
But the problem went beyond Wali Karzai. A UN report for the World Bank published in February 2006 concluded the Afghan heroin trade was operating with the assistance of many top Afghan government officials and under the protection of the Afghan Ministry of Interior.
As evidence of CIA and Afghan government involvement in the heroin trade grew, the focus of the western media shifted towards blaming the Taliban for using drug profits to fund their insurgency against foreign forces.
However, historian Peter Dale Scott challenged this narrative, citing UN estimates that the Taliban’s share of the Afghan opium economy was a fraction compared to that of supporters of the Karzai government. Scott emphasized that the largest share of the drug trade was controlled by those aligned with the Afghan government.
The surge
In early 2010, the Obama administration announced a “surge” of 33,000 US troops to help pacify the country, with a particular focus on key districts known for poppy cultivation. One such district was Marja in Helmand province, which McCoy referred to as “the world’s heroin capital.”
Despite the surge’s mission, US commanders seemed unaware of Marja’s significance as a hub for heroin production, fueled by the surrounding opium fields that accounted for 40 percent of the world’s illicit opium supply.
In September 2010, eight months after the start of the surge, “unsubstantiated” reports emerged that British soldiers were involved in trafficking heroin out of Afghanistan using military aircraft at airports in Camp Bastion and Kandahar.
Camp Bastion, jointly operated by the UK and the US, was located near Lashkar Gah, another major center of poppy cultivation. In 2012, it was alleged that poppy cultivation was taking place just outside the base’s perimeter, with British soldiers providing protection to farmers against Afghan security forces.
By late 2014, British and US forces withdrew from Camp Bastion, handing it over to Afghan forces, who renamed it Camp Shorabak. However, according to a UN report, “the opium-growing area around Britain’s main base in Afghanistan nearly quadrupled between 2011 and 2013.”
Despite the withdrawal, opium exports from Camp Shorabak apparently continued, and a small number of British military personnel returned in 2015 in what was described by the Ministry of Defense as an advisory role.
In 2016, Obaidullah Barakzai, a member of the National Assembly of Afghanistan, claimed, “It’s impossible for a few local drug smugglers to transfer opium in thousands of kilos. This is the work of the Americans and British. They transport it by air from Camp Shorabak.”
After US forces chaotically withdrew from Afghanistan in August 2021, the Taliban once again succeeded in eliminating poppy cultivation, showing it was far from a “dedicated drug cartel” after all.
Follow the money
In November 2021, an opium merchant claimed that “All the profits go to the foreign countries. Afghans are just supplying the labor.”
Peter Dale Scott noted that according to the UN, some $352 billion in drug profits had been absorbed into the western financial system, including through the US’ largest banks in 2009. As a result, Scott said the “United States involvement in the international drug traffic links the CIA, major financial interests, and criminal interests in this country and abroad.”
In 2012, the Daily Mail reported that HSBC, Britain’s biggest bank, faced up to £640million in penalties for allowing “rogue states and drugs cartels to launder billions of pounds through its branches,” and for becoming “a conduit for criminal enterprises.”
The billions in profits flowing from the Afghan heroin trade into western banks have now been eliminated by the Taliban not once, but twice in the past two decades.
Taliban leader Mullah Omar’s pronouncement in July 2000 that poppy cultivation was “un-Islamic” was, therefore, a more likely cause of the US sanctions imposed in December of the same year, and of the US invasion of Afghanistan a year later, than was any US desire to apprehend Bin Laden and dismantle Al-Qaeda.
In March 2002, just six months after the bombing and invasion of Afghanistan, a journalist asked President Bush, “Where’s Osama bin Laden?” Bush replied, ‘I don’t know. I don’t really think about him very much. I’m not that concerned.”
The Afghan drug trade serves as a stark reminder of the intricate connections between geopolitics, illicit economies, and global finance, and the need for greater transparency and accountability in addressing these complex issues.
The historical evidence also challenges the simplistic narrative that the Taliban largely controlled the Afghan drug trade, highlighting the dominant role played by the US-backed Afghan government and its allies in the CIA.
“Fake News” from NBC on US-Russian talks about an ‘off ramp’ to the Ukraine war in April 2023 that never took place
By Gilbert Doctorow – July 6, 2023
News portals in Ukraine and elsewhere in Europe were quick to pick up a feature item today on NBCNews.com entitled “Former U.S. officials have held secret Ukraine talks with prominent Russians.” The subtitle goes on: “The aim of the discussions is to lay the groundwork for potential negotiations to end the war, people briefed on the talks tell NBC News.”
The very notion that such talks could have taken place elicited disparaging comments from the usual suspects who would not miss a chance to be in the public eye: former U.S. ambassador to Russia, Michael McFaul, and Matt Dimmick, a former Russia and Eastern Europe director at the National Security Council. Said comments form part of the NBC report.
This news item also surfaced on Russian state television in the early evening edition of Sixty Minutes under the heading “Fake News.” Their panel discussion opened with an announcement from the RF Ministry of Foreign Affairs, responding to what is said in the second paragraph in the NBC article, which reads:
“In a high-level example of the back-channel diplomacy taking place behind the scenes, Russian Foreign Minister Sergey Lavrov met with members of the group for several hours in April in New York, four former officials and two current officials told NBC News.”
Per Lavrov, no such meeting ever took place and there are no back channels.
And then the Sixty Minutes panel was off to the races, as we say.
They listed the former U.S. officials who were said to have taken part in the meeting – Charles Kupchan, Richard Haass, and Thomas Graham, all members of the Foreign Relations Council and, as they stressed with truculent humor, all are decidedly very former. Their heyday was decades ago and today none of them holds a rank that would justify Lavrov’s spending any time with them, let alone discussing the basic principles for some negotiated settlement of the Russia-Ukraine war. They are just a bunch of old academics who get together to reminisce about the arms control negotiations of the distant past and similar issues long ago laid to rest.
After breaking its fake news story, NBC spent the greater part of its article talking about how back channel communications, dubbed Track Two talks, function and what utility they have in general.
To be sure, backchannels have served a constructive purpose in U.S. – Russian relations in the not too distant past, though I doubt that journalist Josh Lederman has a clue about this. Thomas Graham’s former mentor and associate, Henry Kissinger, had been an important initiator of such an outreach back in the summer-early autumn of 2008 when he, too was a former, not active political actor. But then Kissinger was and is Kissinger, not some flunky. That was in the time just after the Russia-Georgia war, when relations between the two countries were very tense, almost as seriously as today. And, most importantly, at the time Kissinger’s was not the only backchannel operating. In parallel there was another channel headed by a couple of members of the U.S. Senate. The end result was a paper on steps to improve bilateral relations that became known as the ‘re-set’ in the early days of the first Obama administration. Whether that initiative was creative enough to go beyond atmospherics and set the groundwork for a real change in the relationship is a different matter. The answer to that, of course, is ‘no.’
The likes of Kupchan, Haass and Graham cannot be compared to the operators of the 2008 backchannel and it was no wonder that the Sixty Minutes panel thumbed its noses at them. I, for one, have in the past taken the measure of two of these three as thinkers and found that Haass and Kupchan are muddle headed and their writings are mired in contradictions. Supposedly what they write and publish in the house organ Foreign Affairs magazine is peer vetted, but it helps not a whit. When everyone is aligned and no one disagrees, when there are no debates, only back slappers, then the quality of thinking sinks.
See my critique of Kupchan’s article ‘Nato’s final frontier: Why Russia should join the Atlantic Alliance” in Stepping out of Line (2012) pp. 199 -208 and my piece “Richard Haass: the Absent Voice at Valdai-Sochi” in Does Russia Have a Future (2015) pp 259-262
©Gilbert Doctorow, 2023
Walensky Warns Public to Beware of ‘Misinformation’ and ‘Politicized Science’
By Brenda Baletti, Ph.D. | The Defender | July 5, 2023
As she ended her tenure last week as director of the Centers for Disease Control and Prevention (CDC), Dr. Rochelle Walensky warned the American public to be on guard against “misinformation” and the “politicization of science.”
Walensky told The Wall Street Journal she hopes Americans will make health decisions based on “their own risk assessment and their own personal risks, but not through politics,” emphasizing that public health recommendations also shouldn’t be politicized.
“Ironically, this comes after two-and-a-half years of Walensky misinforming the public and politicising the science,” investigative journalist Maryanne Demasi, Ph.D., wrote on her Substack.
Demasi and many others took to Twitter to remind people of Walensky’s false statements and politicized decision-making.
Walensky last week published a farewell op-ed in The New York Times, in which she wrote that public health is critically important in the U.S., and yet she “fear[s] the despair from the pandemic is fading too quickly from our memories.”
She complained that “the agency [CDC] has been sidelined, chastened by early missteps with Covid and battered by persistent scrutiny.”
She also told the WSJ that public health shouldn’t fall along partisan lines.
Yet stark political partisanship defined her time at the CDC. The WSJ reported that a recent KFF poll showed political affiliation was the strongest demographic predictor of COVID-19 vaccination. And about one-quarter of Americans don’t trust the CDC’s health recommendations, according to a 2022 survey published in the journal Health Affairs.
Walensky acknowledged “missteps in communicating” by the CDC, which, she said, “could have done a better job” making it clear to the public that the agency’s message could change during the pandemic.
But, she told the WSJ, the CDC has a plan to regain public trust in the future — by working directly with media organizations to discuss how to best shape public opinion prior to releasing scientific information to the public.
She said the CDC plans to use a method called “prebunking,” where they will communicate directly with media organizations before they release information to let the media know which details about public health might be “misconstrued.”
According to The Associated Press (AP) “prebunking” by public health agencies allows the agencies to define something as “misinformation” before readers have an opportunity to encounter it elsewhere as possibly true.
Then search engines such as Google prioritize “credible websites” like the U.S. Food and Drug Administration’s (FDA) or the CDC’s in its searches.
FDA Commissioner Robert Califf, the Virality Project and Google are among those who have promoted prebunking as a way to combat misinformation.
Journalist Kim Iversen proposed a different approach Walensky might take to restoring public trust in the CDC.
She said:
“Well, the way to do it is to apologize, to own up to your lies, to own up to the mistakes that you made and to discuss why you did that, why the agency followed such political partisanship when they should have been following science, why they ignored the science that was right in front of them.”
CDC broadcast a long list of ‘misinformation’ during Walensky’s tenure
Throughout her tenure at the CDC, which began when Biden took office in January 2021, Walensky made a series of public statements that have proven to be false.
Evidence has since emerged that Walensky knew many of these statements were false when she made them.
In March 2021, Walensky famously told Rachel Maddow, that “vaccinated people do not carry the virus, don’t get sick.”
The CDC was forced to walk back her statements a few days later. But that message was the basis for vaccine mandates imposed later that year by the Biden administration, businesses, universities and public venues throughout the country.
In a mid-June congressional hearing, Walensky defended her March statements, claiming they were true at the time.
But the Washington Examiner reported on June 20 that emails obtained through a Freedom of Information Act request showed Walensky and Dr. Francis Collins were aware of and discussed “breakthrough cases” of COVID-19 in January 2021 — just before the vaccines became widely available — and yet continued to tell the public the vaccines would prevent transmission.
In that same congressional testimony, Walensky also defended the mask mandates, saying that the summary of Cochrane’s review — which found wearing masks in the community “probably makes little to no difference” in preventing viral transmission — had been “retracted.”
But it was neither retracted nor had the authors of the review changed the language in the summary, Demasi reported.
In June 2021, Walensky told “Good Morning America” that the risk of myocarditis was extremely rare, and there was overwhelming data the vaccines were safe for children — even after hundreds of cases of myocarditis had been reported and the CDC had been aware of a safety signal since February.
Under Walensky, the CDC also gave false information on vaccine safety monitoring, added the COVID-19 vaccines to the childhood vaccine schedule despite known harms, withheld data on boosters from the agency’s own advisers and told pregnant women the vaccine was safe — just days after Pfizer reportedly finalized a report demonstrating it wasn’t.
In a March study by Krohnert and others, researchers compiled instances of errors in data presented by the CDC during the COVID-19 pandemic in publications, press releases, interviews and Twitter. The authors reported 25 instances where the agency under Walensky promoted demonstrably false numbers.
In most (80%) cases, the CDC exaggerated the severity of the pandemic. For example, Walensky gave a briefing on June 23, 2022, during which she claimed COVID-19 was a “top 5 cause of death” in children, which was untrue.
Most recently, the House Select Subcommittee on the Coronavirus Pandemic gave Walensky until July 12 to turn over phone records involving American Federation of Teachers (AFT) President Randi Weingarten. The House is investigating potential political interference on the part of AFT with the CDC’s school reopening recommendations during the COVID-19 pandemic, The Defender reported.
Walensky warns of ‘future threats’
Walensky warned at the end of her Times op-ed:
“I want to remind America: The question is not if there will be another public health threat, but when. The C.D.C. needs public and congressional support if it is going to be prepared to protect you from future threats.”
To take on these “future threats” the Biden administration nominated Dr. Mandy Cohen, an internal medicine physician and former state health secretary of North Carolina, to replace Walensky.
But critics warn Cohen is “a public health COVID authoritarian” who is “fully entrenched in the ‘bio-pharmaceutical complex.’”
Dr. Peter McCullough told The Defender that during the COVID-19 pandemic, Cohen failed to recognize therapeutics and natural immunity, and supported lockdowns, vaccine mandates and masking.
Cohen comes to the CDC from the private sector, where she is executive vice president of Aledade and CEO of Aledade Care Solutions, whose executive leadership and board of directors includes people with connections to the World Economic Forum and the Bill & Melinda Gates Foundation.
Walensky congratulated Cohen on her nomination, describing her as “a respected public health leader who helped North Carolina successfully navigate” COVID-19, and whose “unique experience and accomplished tenure in North Carolina … make her perfectly suited to lead CDC as it moves forward by building on the lessons learned from COVID-19 to create an organization poised to meet public health challenges of the future.”
Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.
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.
Dr. Paul Offit Lets Us Know ‘the Experts’ Have Officially Lost Their Minds
By Madhava Setty, M.D. | The Defender | July 5, 2023
I don’t have a big presence on Twitter. I don’t find the platform suitable for exploring and critiquing interesting ideas. You can say only so much in 280 characters. It’s great for inciting someone or dropping a witty comeback or link without much context.
At least that’s what I thought. Then I stumbled upon a tweet from Dr. Paul Offit. He’s taught me that you can convey a lot in a few short sentences.
Who is Dr. Paul Offit?
Offit is a big name in vaccines. Beyond what is listed below, he also sat on the Advisory Committee on Immunization Practices for the Centers for Disease Control and Prevention (CDC) and is presently a member of the Vaccines and Related Biological Products Advisory Committee for the U.S. Food and Drug Administration (FDA).
He’s had a say in the approval and/or authorization of many biologics, including the COVID-19 mRNA products.
Briefly, Offit is:
- Director of the Vaccine Education Center and professor of pediatrics in the Division of Infectious Diseases at Children’s Hospital of Philadelphia.
- Maurice R. Hilleman Professor of Vaccinology at the Perelman School of Medicine at the University of Pennsylvania.
- An internationally recognized expert in the fields of virology and immunology.
- A founding advisory board member of the Autism Science Foundation and the Foundation for Vaccine Research.
- A member of the Institute of Medicine and co-editor of the foremost vaccine text, “Vaccines.”
- The author or co-author of more than 150 papers in medical and scientific journals in the areas of rotavirus-specific immune responses and vaccine safety.
- The co-inventor of the rotavirus vaccine, RotaTeq®, recommended for universal use in infants by the CDC.
- A recipient of the Charles Mérieux Award from the National Foundation for Infectious Diseases.
His list of accomplishments goes on.
I don’t pretend to know more about vaccines than he does. I’m just an anesthesiologist and engineer. He must be a very smart person. Which is why this tweet is so baffling:

Why is Offit tweeting about placebos and saltwater right now?
It has to do with a truth bomb Robert F. Kennedy Jr. dropped at a town hall event last week.
According to Kennedy, chairman on leave from Children’s Health Defense, he and attorney Aaron Siri sued the U.S. Department of Health and Human Services (HHS) after HHS refused to meet their demand to produce at least one study comparing the safety of a vaccine on the childhood immunization schedule with a true placebo.
In a written response received more than a year later, the HHS did not cite a single such study, instead claiming:
“Inert placebo controls are not required to understand the safety profile of a new vaccine, and are thus not required.”
This stupefying claim made by Melinda Wharton, M.D., MPH, acting director of the National Vaccine Program Office, should be attacked on podcasts and publications everywhere.
How do you know that a new vaccine is safe if it isn’t tested against an inert placebo, Dr. Wharton?
If you are someone who is willing to abandon basic logic and trust every single word spewed by our public health agencies, ask yourself, why then does the FDA demand that medicines be tested against a placebo to ensure safety prior to licensure?
Twitter lit up around this pivotal topic. The tweet from one of the foremost vaccine experts in the world (Offit) was in response to Siri, who, according to Offit, asserted that virtually all vaccines on the childhood vaccination schedule, including RotaTeq (Offit’s brainchild), were not licensed by the FDA based on a placebo-controlled clinical trial.
Let’s break down Offit’s attack on Siri. Offit states: “The purpose of placebos, which are immunologically inert, is to determine the effect of the vaccine.”
Yes, Dr. Offit, one purpose of a placebo is to determine the effect of the vaccine. In order to prove that it works, it must do better than an immunologically inert substance. In other words, it must exceed the so-called placebo effect.
But that’s not the only purpose placebos serve. With regard to safety, a new vaccine has to be compared to something that has the least possible chance of causing deleterious effects.
To be clear, those who eschew a vaccine do not get in line for a shot of an “immunologically inert substance.” They stay away from the vaccine clinic altogether and take their chances.
This is why the placebo must be a true placebo. The best we can possibly do is use saline, a saltwater solution that reasonably matches the sodium concentration in our plasma. It is what is used to dilute medications and replenish blood volume. It’s what you use to store your contact lenses.
Offit then adds this:
“[Aaron Siri] believes that only water or salt water are placebos because they ‘have no effect on living beings.’ That’s absurd. Drink enough water, and you can cause a seizure. Salt can also be toxic.”
Offit is saying that by drinking a large amount of water the plasma sodium concentration in a person can abruptly decrease which, in fact, can lower the seizure threshold. He’s not wrong, it does happen in pathological conditions, especially in the critically ill.
Can salt be toxic? Yes. Ingestion of a large amount of salt will stimulate properly functioning kidneys to increase the absorption of free water, thus mitigating the effect of the salt load. This can cause volume overload and put a person at risk for heart failure and pulmonary edema.
So what — if not 0.2 ml of saline — should we use for a placebo, Dr. Offit? A tiny aliquot of adjuvants (that can include elements like aluminum)? Pro-inflammatory lipid nanoparticles? Viral or toxin deactivators like formaldehyde? Preservatives like thimerosal that contain mercury, one of the most potent neurotoxins known (yes, mercury in this form is still in some flu vaccines according to the CDC)?
All of these substances are “immunologically inert.”
But why would you consider using them as a placebo control if not to mask the potential harm of the vaccine in question?
Is that how inventors of vaccines for our children view placebos? Is that how advisory committee members on the FDA view them? What about the other advisory board members of the Autism Science Foundation? Why would anyone trust any vaccine on the childhood immunization schedule after such comments?
You don’t have to be Maurice R. Hilleman Chair of Vaccinology at the Perelman School of Medicine to see that your comments here are misleading, disingenuous and purposefully inciting.
Moreover, they don’t make any sense.
What would other recipients of your long list of awards have to say about your comments on placebos? I don’t think they would approve, sir.
Your public statements also sully the excellent reputation of the Children’s Hospital of Philadelphia and those who were lucky to train there, like me.
Dr. Setty has been a board certified anesthesiologist since 2002 and has held various leadership positions in his clinical practice.
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.
Government Contracts With COVID Vaccine Makers Let Federal Agencies Bypass Normal Regulatory Process: FOIA Docs
By Brenda Baletti, Ph.D. | The Defender | June 30, 2023
A little-known federal agency called BARDA dedicated to countering “health security threats” was responsible for conducting the quality review of every COVID-19 vaccine dose administered in the U.S., Sasha Latypova reported on her Substack.
But BARDA, the Biomedical Advanced Research and Development Authority, which has a “militarized” purpose according to Latypova, is not subject to the same regulations as typical pharmaceutical manufacturers, distributors or regulatory agencies.
Distribution through BARDA was part of the “bait and switch” the federal government subjected the American people to with the COVID-19 vaccines, Latypova — a former pharmaceutical industry executive who now exposes fraud in COVID-19 countermeasures — told The Defender in an interview.
“The public was told these vaccines are made by Pfizer and Moderna and rigorously approved by the FDA.” That, she said, would mean that the “consumer protections we expect from pharmaceutical products, medical devices and even food — which are huge and extensive — we expect them to be in place.”
But in fact, countermeasures contracts made available through Freedom of Information Act (FOIA) requests by various parties and U.S. Securities and Exchange Commission disclosures show the U.S. Department of Defense (DOD) and BARDA contracts with the pharmaceutical companies were structured such that these protections weren’t required, according to Latypova.
The contracts also specified that manufacturers and federal agencies were protected by the Public Readiness and Emergency Preparedness (PREP) Act, which shields “covered persons” — such as pharmaceutical companies, or the DOD/BARDA — from liability for injuries sustained from “countermeasures,” such as vaccines and medications administered during a public health emergency.
Latypova posted a video of a November 2022 presentation during which BARDA’s then-director of Regulatory and Quality Affairs (RQA) Tremel Faison bragged that before the U.S. government could purchase and release any COVID-19 product, the RQA team had to perform a review and acceptance.
“I thought it was very strange, given that this is technically the FDA’s [U.S. Food and Drug Administration] job,” Latypova wrote, so she investigated BARDA.
BARDA is housed within the U.S. Department of Health and Human Services, but its purpose is “to develop medical countermeasures that address the public health and medical consequences of chemical, biological, radiological, and nuclear (CBRN) accidents, incidents and attacks, pandemic influenza, and emerging infectious diseases.”
BARDA now functions as part of the Office of the Assistant Secretary for Pandemic Preparedness and Response, elevated by the Biden administration in 2022 to coordinate the nation’s response to health emergencies.
BARDA reports that it has 77 products on the market.
This is concerning, Latypova said, because typically pharmaceutical products are subject to regulations that govern the clinical trial and manufacturing process and then the licensed pharmacy distribution system monitors for consumer safety.
They are subject to “cGxP” regulations, a suite of “current good practice” processes and procedures with the “x” standing in for a variety of life sciences areas, including manufacturing, laboratory, clinical and distribution.
Those regulations create tight control over pharmaceutical products ensuring, for example, that labeling is accurate, dosage is accurate, there are no impurities, and the active ingredients are active and present in the proper amounts.
The regulations also establish supply chain regulations so the products are tracked during transportation and distribution and are traceable, and they protect consumers from drugs being counterfeit, stolen, contaminated or otherwise harmful.
According to Latypova, the fact that BARDA receives and quality checks the vaccines means the vaccines and COVID-19 countermeasures are subject to different protocols than typical FDA-approved or FDA-authorized products.
According to BARDA’s Standard Operating Procedure (SOP) documents outlining its procedures for receiving and inspecting medical countermeasure products, which Children’s Health Defense obtained through a FOIA request, materials ordered by BARDA have their own process of approval.
Products are shipped from the manufacturer to BARDA. Prior to delivery, BARDA receives the lot number and a certification from the producer that says the product meets its established specifications and contains other technical information such as lot number, etc.
BARDA’s RQA team then receives sealed trucks, makes sure documentation is in order and temperature control is maintained, watches the unloading, and “conducts a cursory examination of obvious physical damage.”
BARDA does not test or verify the contents of the vials it receives. It simply accepts the claims in the manufacturers’ paperwork.
And the products from BARDA, according to the SOP, go into storage at a Strategic National Stockpile site, which, unlike typical pharmaceutical storage sites, is also not subject to regulations.
Pharmacy distribution is licensed on a state-by-state basis. Those regulations are typically extensive as seen, for example, in the Pharmacy Lawbook for the state of California that Latypova posted.
It was previously known that the FDA exempted COVID-19 countermeasures from many of these requirements, justifying that exemption based on the public health emergency.
In May, the FDA extended that exemption beyond the May 11 end of the COVID-19 public health emergency.
But the BARDA documents reveal how limited the oversight provided for the receipt and inspection of countermeasures is in practice.
Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.
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.
Three Typhoon Jets Landed Next to Thermometer When Britain’s ‘Record’ Temperature of 40.3°C Was Recorded
BY CHRIS MORRISON AND IAN RONS | THE DAILY SCEPTIC | JUNE 28, 2023
At least three Typhoon fighter jets were landing at RAF Coningsby around the time when the brief U.K. temperature record was declared at 15:12 on July 19th last year from a measuring device situated halfway down the runway. Following a Freedom of Information request, the Daily Sceptic has obtained portions of the log books of four pilots flying from the base that afternoon, casting considerable doubt on the record that made headlines around the world.
The pilots’ log books record three of the four Typhoons landing at 15:10, 15:15 and 15:15. However, since these log books round off all times to the nearest five minutes, we can interpret this to mean the three jets landed between about 15:07:30 to 15:17:30 at the latest. But pilots want to rack up the most possible flying hours, so a landing at 15:12:30 would be written down as 15:15 and not 15:10, and there is always wiggle room.
In reality, it’s likely that the three jets actually landed in very quick succession, rather than over the space of several minutes. Many videos are available online showing operations at Coningsby, with Typhoons flying (and landing) close to each other, and a very recent video shows three jets landing within 30 seconds. The lead jet of the three landing on July 19th was ZJ914 – the RAF’s primary display aircraft – suggesting the others were experienced pilots who may well have landed in close formation. Taken in context with the log books, this points to the three aircraft landing together at some point very close to when the record was set at 15:12, and likely a little before.
At 15:10, the temperature suddenly jumped by 0.6°C to hit the 40.3°C record at 15.12. Within 60 seconds, the record temperature dropped back by 0.6°C. At the time, the Met Office claimed that verifying the record had been a “rigorous process” and that all data was accurate.
The Daily Sceptic has published a number of articles about the Coningsby incident and the general recording of surface temperatures by the Met Office. Last November, we asked the Met Office if its “rigorous process” confirming the validity of the 40.3°C record had ruled out all non-climatic causes such as jet aircraft operating near the measuring device, since RAF Coningsby is a major jet pilot training centre and home to two squadrons of Typhoons. We received no reply. Earlier, Lincolnshire Live was told the rise in temperature might have been due to a break in thin cloud. Last November, the Daily Sceptic published a satellite photo showing cloudless skies at 15:00 on July 19th across London and most of eastern England.
In the light of our latest revelations, it’s time the Met Office made a statement about its claimed record at RAF Coningsby. It should either withdraw it, or provide convincing evidence as to why the record should be retained. If it does not take public action, it risks the ‘record’ becoming a national joke.
Last year was a warm year in the U.K. and July 19th was undoubtedly a very hot day, although the mini-heatwave had broken by 22:00, with rain in London and a 20°C drop in temperature. Five English places declared temperatures over 40°C, but all have problems with non-climatic heat corruptions.
The World Meteorological Organisation (WMO) grades weather stations and gives lower classifications to those surrounded by tarmac and buildings. An interesting article in the blog Climate Scepticism looked at the five U.K. 40°C sites and found problems at all of them. According to the WMO, the classification set for Coningsby suggests a temperature margin of error of up to 1°C. The second place at London’s St. James’s Park is sited next to a metalled path, suggesting a 2°C uncertainty. Heathrow and Northolt are busy London airports with the same problems as Coningsby. The last site in Kew Gardens is marginally better, but it is sited near one of the largest tropical greenhouses in the world, and breezes wafting over the vast glass structure could corrupt surrounding measurements.
For the purpose of taking temperature measurements to build a picture of long-term climate change, there are few places more unsuitable than an airport runway. But all airports measure temperature for operational purposes, and the easily-available data from numerous locations is embedded in both national and international datasets. In the U.K., the Met Office is fully signed up to the ‘climate crisis’ narrative. One-off weather events and measurements are fed to the unquestioning mainstream media by the Met Office and this helps promote alarm in the cause of the collectivist Net Zero agenda. The Met Office is particularly busy in the summer months where it seems to have decided to catastrophise what was once considered normal summer weather. Three balmy days of 25°C on the Cornish Riviera are now termed a ‘heatwave’, while national weather maps turn blood-red as temperatures climb through the 20s. On a global scale, the Met Office has retrospectively added over 30% warming to the last 20 years, removing a 2000-2012 pause clearly still seen in satellite data.
At the time of the claimed Coningsby record, Dr. Mark McCarthy from the Met Office told Lincolnshire Live that in a climate unaffected by human-induced climate change “it would be virtually impossible for temperatures in the UK to reach 40°C”. There is no way that McCarthy can know this since it is just an opinion, or to be more accurate, an opinion backed up by computer models. There is not a single science paper that would prove that claim conclusively.
If anything, it would seem that much of the claimed urban heat should be removed, rather than increased. In recent ground-breaking work, two American scientists – Dr Roy Spencer and Professor John Christy – working out of the University of Alabama in Huntsville, have started to separate out the effect of urbanisation on temperature measurements. Over the last 50 years, it was discovered that warming could have been exaggerated by up to 50% across the eastern United States. Interestingly, the largest exaggerations were found at airports. At Orlando International Airport in Florida, the local data showed massive warming of 0.3°C per decade, a figure that fell to just 0.07°C when adjusted for urban heat.
CISA Was Behind the Attempt to Control Your Thoughts, Speech, and Life
Brownstone Institute | June 30, 2023
Keeping up with the corruption of the Covid regime feels like drinking from a firehose. The volume of the fraud, the pace of new discoveries, and the breadth of the operations are overwhelming. This makes it imperative for groups like Brownstone Institute to digest the onslaught of information and communicate salient themes and dispositive facts, particularly given the dereliction of mainstream media.
On Monday, the House Judiciary Committee released a report on how the Cybersecurity and Infrastructure Security Agency (CISA) “colluded with Big Tech and ‘disinformation’ partners to censor Americans,” adding to the informational firehose we work to imbibe.
The 36-page report raises three familiar issues: first, government actors worked with third parties to overturn the First Amendment; second, censors prioritized political narratives over truthfulness; and third, an unaccountable bureaucracy hijacked American society.
- CISA’s Collusion to Overturn the First Amendment
The House Report reveals that CISA, a branch of the Department of Homeland Security, worked with social media platforms to censor posts it considered dis-, mis-, or malinformation. Brian Scully, the head of CISA’s censorship team, conceded that this process, known as “switchboarding,” would “trigger content moderation.”
Additionally, CISA funded the nonprofit EI-ISAC in 2020 to bolster its censorship operations. EI-ISAC worked to report and track “misinformation across all channels and platforms.” In launching the nonprofit, the government boasted that it “leverage[d] DHS CISA’s relationship with social media organizations to ensure priority treatment of misinformation reports.”
The switchboard programs directly contradict sworn testimony from CISA Director Jen Easterly. “We don’t censor anything… we don’t flag anything to social media organizations at all,” Esterly told Congress in March. “We don’t do any censorship.” Her statement was more than a lie; it omitted the institutionalization of the practice she denied. The agency’s initiatives relied on a collusive apparatus of private-public partnerships designed to suppress unapproved information.
This should sound familiar.
Alex Berenson gained access to thousands of Twitter communications that uncovered concrete evidence that government actors – including White House Covid Advisor Andy Slavitt – worked to censor him for criticizing Biden’s Covid policies.
White House Director of Digital Strategy Rob Flaherty privately lobbied social media groups to remove a video of Tucker Carlson reporting the link between Johnson & Johnson’s vaccine and blood clots.
Facebook worked with the CDC to censor posts related to the Covid “lab-leak” hypothesis. Company employees later met with the Department of Health and Human Services to de-platform the “disinformation dozen,” a group including Robert F. Kennedy, Jr.
These were not cherry-picked examples – they were part of an institutional collusion to strip Americans of their First Amendment rights. Journalists Michael Shellenberger and Matt Taibbi exposed the “Censorship Industrial Complex,” a collection of the world’s most powerful government agencies, NGOs, and private corporations that worked together to silence dissent.
The Supreme Court has held that it is “axiomatic” that the government cannot “induce, encourage, or promote private persons to accomplish what it is constitutionally forbidden to accomplish.” Yet, CISA has joined the disturbing tendency of public-private partnerships designed to impede Americans’ right to information and freedom of speech.
- Political Operatives
Second, these programs were not idealistic attempts to promote the truth; they were calculated programs designed to quash inconvenient but truthful narratives.
The report outlines how CISA censored “malinformation – truthful information that, according to the government, may carry the potential to mislead.” Journalist Lee Fang later wrote that the malinformation campaign “highlights not only the broad authority that the federal government has to shape the political content available to the public, but also the toolkit that it relies upon to limit scrutiny in the regulation of speech.”
In this system, uncensored information has a tacit government approval, amounting to a system of widespread propaganda.
“State and local election officials used the CISA-funded EI-ISAC in an effort to silence criticism and political dissent,” the report notes. “For example, in August 2022, a Loudon County, Virginia, government official reported a Tweet featuring an unedited video of a county official ‘because it was posted as part of a larger campaign to discredit the word of’ that official. The Loudon County official’s remark that the account she flagged ‘is connected to Parents Against Critical Race Theory’ reveals that her ‘misinformation report’ was nothing more than a politically motivated censorship attempt.”
The officials supporting the operation remained unrepentant in their aim to advance political agendas. Dr. Kate Starbird, a member of CISA’s “Misinformation & Disinformation” subcommittee, lamented that many Americans seem to “accept malinformation as ‘speech’ and within democratic norms.”
Of course, the program explicitly violated the Constitution. The First Amendment does not discriminate based on the veracity of a statement. “Some false statements are inevitable if there is to be an open and vigorous expression of views in public and private conversation,” the Supreme Court’s controlling opinion held in United States v. Alvarez. But CISA – led by zealots like Dr. Starbird – appointed themselves the arbiters of truth and worked with the most powerful information companies in the world to purge dissent.
This was part of a larger political campaign.
Hunter Biden’s laptop, natural immunity, the lab-leak theory, and side effects of the vaccine were all censored at the government’s behest. The truth of the reports were not at issue; instead, they presented inconvenient narratives for Washington’s political class, who then used the Orwellian label of “malinformation” to lend cover to eviscerating the First Amendment.
- The Terror of the Administrative State
Third, the report exposes the increasing power of the administrative state. Federal bureaucrats rely on anonymity and unaccountability. Private industry employees could never oversee a disaster like the Covid response and maintain their jobs. It’d be like if BP’s head of safety for the Gulf of Mexico received a promotion after the oil spill.
But unelected officilals like CISA officials enjoy ever-increasing power over Americans’ lives without having to answer for their calamities. Suzanne Spaulding, a member of the Misinformation & Disinformation Subcommittee, warned that it was “only a matter of time before someone realizes we exist and starts asking about our work.”
Spaulding’s comment reflects the power that CISA wields and the benefit it derives from its lack of public exposure. Most Americans have never heard of CISA despite its overwhelming influence over lockdowns.
In March 2020, CISA divided the American workforce into categories of “essential” and “nonessential.” Within hours, California became the first state to issue a “stay at home” edict. This began a previously unimaginable assault on Americans’ civil liberties.
The House Report indicates that CISA was a central actor in censoring criticism of the Covid regime in the ensuing months and years. The agency is representative of the cabal of censorial and unaccountable officials engaged in public-private partnerships designed to keep us in the dark.
RFK Jr. Dismantles Doctor’s Pro-Vaccine Stance in Town Hall Meeting
By Madhava Setty, M.D. | The Defender | June 29, 2023
Epistemology is the theory of knowledge. Epistemologists ask the foundational question, “How do we know what we know?”
Robert F. Kennedy Jr. on Wednesday appeared in a town hall meeting hosted by NewsNation and moderated by journalist Elizabeth Vargas.
The exchanges between Kennedy — chairman on leave from Children’s Health Defense — Vargas and Dr. Tariq Butt, a family medicine doctor in the audience, demonstrated the real quagmire the scientific community finds itself in.
Doctors and journalists cannot see the difference between believing and knowing. If we were in a rational world, there wouldn’t be the need for censorship and shadowbanning.
Nor would many of the vaccines on the childhood immunization schedule, as presently formulated and tested, have found their way into the arms of young human beings.
In 13 short minutes, Kennedy deftly demonstrated to the audience that our problem isn’t just a failure of epidemiology — it’s one of epistemology:
Vargas first framed the topic this way:
“The biggest controversy surrounding your candidacy is your stance on childhood vaccines. Nearly every scientific and medical organization including the CDC [Centers for Disease Control and Prevention], the FDA [U.S. Food and Drug Administration], the AMA [American Medical Association], the American Academy of Pediatrics, all say you’re wrong on this issue.”
Vargas opened the door for Kennedy to not only clarify his position — which he said has been distorted and misrepresented no matter how many times he has tried to set the record straight — but she also revealed how little thought and research she has done into the controversy.
Kennedy pointed out the reality of the situation. These are not organizations that have independently arrived at their conclusions. The AMA, the American Academy of Pediatrics and “nearly all scientific and medical organizations” take information coming from the CDC and FDA as gospel.
In other words, if the CDC and the FDA are wrong, the entire medical establishment is wrong.
There’s a difference between consensus and herd mentality — a fact that never seemed to register with Vargas.
Kennedy is immensely knowledgeable about vaccine science and the regulatory process, as well as its corruption by Pharma interests. Moreover, he is a seasoned litigator and is not careless in his delivery. He correctly asks Vargas for clarification: “On what issue?”
Vargas first alludes to the possibility that vaccines could be the cause of autism and harm.
Kennedy immediately asks the obvious, “So you are saying that these organizations claim that vaccines NEVER damage kids?”
Vargas is forced to backpedal:
“I don’t think anyone is saying they never have. There may be a child here [or there], but overall vaccines have saved millions and millions of lives.”
Vargas is demonstrating the lack of understanding the public has about the issue. How can anyone claim that vaccines have saved millions and millions of lives if proper prospective studies with matched unvaccinated controls have never been conducted?
Kennedy makes this abundantly clear in his response to Dr. Butt, who asks Kennedy this question:
“Eradication of chicken pox and polio in the U.S. and in many parts of the world is a result of regular vaccination. MMR [measles, mumps, rubella] and many diseases are preventable. There is little evidence of these diseases in the vaccinated population. Your vaccine stance is dangerous to the health and well-being of millions. Medical experts are deeply concerned about your message. How can we help you come to the side of science?”
Kennedy admits there is evidence that vaccines have reduced the risk of mortality and morbidity from the diseases they target. However, he argued, without long-term prospective studies around all-cause mortality/morbidity in vaccinated populations nobody — no matter how educated or how big an organization you represent, he said — can claim there is an overall benefit.
Kennedy’s answer to the question dismantles the issue to the very core, catching Dr. Butt off guard. His methodical response should have proven to the audience that the family medicine doctor has very little grasp of all the available evidence.
Dr. Butt clearly wasn’t aware of analyses like this one that concluded that a “Mass varicella vaccination is expected to cause a major epidemic of herpes zoster, affecting more than 50% of those aged 10-44 years at the introduction of vaccination.”
Should studies like this guide public policy in the U.S.? They certainly do in the U.K., where health officials do not recommend universal vaccinations against chickenpox for precisely the reason Kennedy states.
Of all the preventable diseases out there, why would Dr. Butt use chickenpox as an example of how Kennedy’s vaccine stance is dangerous to the health and well-being of millions? Could it be that a doctor with a microphone was unaware of the science?
Was Dr. Butt aware of the enormous tragedy caused by the DTP (diptheria, tetanus, pertussis) vaccine in Africa? After 30 years of observation, it was shown that children vaccinated with the DTP shot were dying of other causes at 10 times the rate of the unvaccinated. We would have never known about this if no one actually looked.
The devastation caused by the DTP vaccine is not limited to the continent of Africa. Kennedy informed the audience that the flurry of lawsuits against manufacturers of this vaccine led to the passing of the National Childhood Vaccine Injury Act of 1986, which has protected vaccine manufacturers from any liability.
As a concession to the public, this law also created the Vaccine Adverse Event Reporting System, or VAERS, to “protect” and warn the public of potential vaccine danger; a system that has been shown to underreport injuries as commonly as it gets ignored.
Though Kennedy did not discuss the MMR and polio vaccines, his point was clear: Unless proper, long-term, prelicensure placebo-controlled safety studies are done we cannot determine if more harm than good is being done.
Dr. Butt’s response to the likely damage caused by the varicella and DTP vaccines was all too predictable: “A person can take a medicine and then get involved in a motor vehicle accident.” In other words, correlation does not prove causation!
Dr. Butt has good intentions. He is also particularly skilled at picking the weakest examples to prove his point.
The issue with the varicella vaccine was the resulting increased risk of herpes zoster infection (shingles). The issue with the DTP vaccine was the increased risk of death from other prevalent diseases that proved to be more deadly for the kids who received the vaccine.
We are not talking about random traumatic injuries that have nothing to do with immune modulation.
Furthermore, was Dr. Butt aware that the “correlation does not equal causation” argument can be used to dismiss vaccine benefits as well?
This double standard is mindlessly applied by vaccine proponents. Trials don’t prove causation, only correlation. That goes for efficacy too. On what grounds can one say that a vaccine caused a decrease in the disease it targets while assuring us that it was only correlated with an increase in side effects?
Trials just measure the incidence of things in two (or more) groups of participants. It’s a mathematical comparison. No causation is ever proven.
Vargas took issue with Kennedy’s claim that not one vaccine on the childhood immunization schedule has been subjected to a prelicensured placebo-controlled trial.
Vargas: “Yes they have.”
Kennedy: “No.”
Vargas: “Yeah, they have!”
And later …
Vargas: “The FDA says, and in fact, on its website, you can clearly see vaccines go through three stages of testing against double-blind placebo. They already DO that testing.”
Kennedy: “Elizabeth, you can say that.”
Vargas: “I’m not saying that. The FDA is saying that.”
Kennedy: “The FDA is not saying that.”
Vargas: “Yes they do! They say that on their website!”
Kennedy: “They will not tell you that there’s a vaccine that has ever undergone a long-term placebo-controlled trial prior to licensing because it’s not true.”
The reason why this embarrassing (and mildly entertaining) spectacle is important to dissect is because of what it reveals about the stubbornness we have about being right. Did Vargas actually scour the FDA website prior to this public exchange?
She couldn’t have for the obvious reason that no such statement from them exists on their website as she maintained.
Why is she so sure that she is right? I would venture to say it is because someone whom she trusts more than Kennedy told her that.
But was she really listening to what Kennedy was saying? Kennedy demanded a citation from Dr. Anthony Fauci in a face-to-face meeting with him in 2016. Fauci couldn’t produce one but promised he would.
He never did — so Kennedy (and attorney Aaron Siri) sued him and the U.S. Department of Health and Human Services (HHS). After a year of litigation, they finally obtained a written statement from the HHS which still does not cite a single study but assures us that inert placebos are not required to demonstrate safety in childhood vaccines.
Of course, there is no reason Vargas should trust Kennedy if she has not visited the Children’s Health Defense website where the letter from the HHS is made available.
But at what point should she have paused and honestly asked herself about what she really knew and not just what she thought she did?
In this case, the spectacle arose not because Vargas was wrong, but because she was so sure she was right.
It’s also worthwhile to consider what was on the line for her, personally. Was she able to face the possibility that the vaccines we have been injecting into our own bodies and our children have never been tested against a placebo?
Her argumentative responses to Kennedy’s views, which he defended with several key citations off the top of his head, reflected the real impediments the public has toward seeing reality for what it is. What would it mean if Kennedy has been right all along?
As a veteran journalist for NewsNation and previously for Fox and A&E Networks, Vargas should have come prepared. Kennedy has previously made himself very clear that he is willing to change his mind. “Show me where I got it wrong.”
Kennedy asks Vargas to cite a single prelicensure, placebo-controlled vaccine study. She couldn’t because no one can. There aren’t any.
Kennedy pointed out the real issue: “We have a corrupt federal agency [FDA] that is lying to the AMA and all those agencies and all those doctors. But those agencies are controlled by Pharma. That is the problem.”
Without any studies to cite or any way to refute Kennedy’s damning allegations, Vargas chose to confront Kennedy with the fact that some of his family members disagree with his stance on vaccines.
Kennedy: “Does your family agree with everything that you say?”
Vargas: “Definitely not. You got me on that one.”
Madhava Setty, M.D. is senior science editor for The Defender.
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.
Religious Exemption Form for Parents of School-Age Kids in D.C. ‘Intentionally Misleading and Unlawful’
The Defender | June 27, 2023
A form provided by the District of Columbia Department of Health for parents seeking a religious exemption for mandated vaccines on behalf of their minor children is “intentionally misleading and unlawful,” according to Children’s Health Defense (CHD) Senior Staff Attorney Rolf Hazlehurst.
A letter from Hazlehurst and CHD Acting President Laura Bono to D.C. Mayor Muriel Bowser and school and health department officials states there is “no legal basis or requirement” for parents to use the newly revised “2023 Religious Exemption Request Process for Families” posted on the DC Health website.
According to the health department, “In consideration of the COVID-19 vaccine mandate for eligible students, and the need to ensure all students in the District remain up to date with all necessary or required vaccinations to attend school,” health officials revised the religious exemption form “to include a section to document a strongly held religious belief opposing vaccination.”
Parents and guardians are instructed to request the form and return it directly to DC Health/Immunization Division after carefully reading and completing it in its entirety. “incomplete or non-compliant forms will be returned before being sent for review, the department said.
But the updated form contains at least two subsections that are “unlawful as written and applied,” Hazlehurst said.
In the first part of Section 2, parents and guardians are required to initial to acknowledge that “by not vaccinating their child for one or more of the listed vaccinations, they are placing their child at ‘increased risk,’ thus implying that they are unfit parents or guardians.”
And, according to the letter, the second part of Section 2 requires each parent or guardian to:
“Please provide a written statement on a) why you do not get vaccinations based on your sincerely held religious beliefs, b) the religious principles that guide your decision not to get vaccinated, and c) whether you are opposed to all vaccinations, and if not, d) the religious beliefs you follow that will not allow you to get the COVID-19 vaccination.”
In their letter, Bono and Hazlehurst said this language “intentionally misleads those parents or guardians seeking religious exemptions into believing they must comply with these instructions or their request will be denied.”
“Nothing could be further from the truth,” they wrote, adding that according to the law, Code of the District of Columbia §38-506, entitled “Exemption from Certification” states:
No certification of immunization shall be required for the admission to a school of a student:
(1) For whom the responsible person objects in good faith and in writing, to the chief official of the school, that immunization would violate his or her religious beliefs.
In other words, parents and guardians are not required to complete the updated form — they can simply write a letter to the chief official of the child’s school certifying that in accordance with the Code of the District of Columbia §38-506, they object in good faith that immunization(s) violate their sincerely held religious beliefs.
If DC Health officials wanted to create a new process in which parents and guardians must comply to receive a religious exemption, the agency is required by law to promulgate the new rule by complying with the administration process and allowing the public the opportunity to respond — neither of which were done, Hazlehurst and Bono wrote.
D.C. Council weighs bill to remove COVID vaccine mandate for schools
Hazlehurst and Dr. Elizabeth Mumper last week submitted written testimony to D.C. Council members in support of Bill 25-0278, the School Student Vaccination Amendment Act of 2023, which would remove the COVID-19 vaccine mandate for students attending D.C. schools.
Both commended the council members for introducing the amendment. In his written statement, Hazlehurst called on the council to expedite passage of the bill “to avoid parents unnecessarily getting their children the COVID-19 vaccine in order to attend school.”
He also outlined his legal objections to the health department’s newly revised religious exemption form.
Mumper, a pediatrician, also showed support for the bill. In a lengthy written statement, she said:
“As a pediatrician with 43 years of experience in pediatrics and 24 years of experience identifying and treating children with vaccine injuries, I oppose giving COVID-19 vaccines to infants and children.
“Having carefully studied the risks and benefits, I conclude unequivocally that the risk of harm outweighs any potential benefit. Multiple sources of scientifically sound data support my position.”
In July 2022, The Washington Post said the district’s COVID-19 vaccine mandate for schoolchildren was “among the strictest in the nation.”
CHD last year represented a group of parents challenging the D.C. Minor Consent for Vaccination Act, which would have allowed children as young as 11 to consent to vaccination without parental knowledge or consent.
CHD fought, and the court issued a preliminary injunction prohibiting enforcement of the law and the district was forced to repeal it.
In his ruling, Judge Trevor N. McFadden said:
“States and the District are free to encourage individuals, including children, to get vaccines. But they cannot transgress on the Program Congress created. And they cannot trample the Constitution.”
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.


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