‘Jaw-Dropping’ Evidence Syngenta Knew Its Paraquat Weedkiller Could Cause Parkinson’s
By Suzanne Burdick, Ph.D. | The Defender | January 19, 2023
Swiss chemical giant Syngenta and Chevron USA for decades covered up research showing long-term exposure to the weedkiller paraquat could cause the incurable brain ailment known as Parkinson’s disease, internal documents reveal.
“It’s jaw-dropping information because at the same time, the companies were saying publicly the opposite — that this chemical did not get into the brain,” investigative journalist Carey Gillam told Robert F. Kennedy, Jr., chairman and chief litigation counsel for Children’s Health Defense, during an episode of “RFK Jr. The Defender Podcast.”
Gillam, author of “The Monsanto Papers: Deadly Secrets, Corporate Corruption, and One Man’s Search for Justice,” has more than 30 years of experience reporting on corporate America and food and agricultural policies
Introduced in the 1960s, paraquat is a highly toxic herbicide that was banned in the EU in 2007 but is still widely used today by U.S. farmers.
Syngenta manufactures paraquat, Chevron USA distributes it in the U.S.
Since “almost day one,” Gillam said, the companies knew the chemical crossed the blood-brain barrier and entered the brain, and that it could have chronic effects on the central nervous system.
“And you see in the 1970s, how the evidence is continuing to mount and how the companies are discussing internally — their scientists and others are discussing amongst themselves — how worrisome it is that all of this evidence of an impact on the brain, a chronic long-term impact on the brain from Parkinson’s, is starting to get stronger and stronger,” Gillam said.
Despite “abundant evidence,” the companies adamantly claimed publicly that the chemical did not cross the blood-brain barrier and continued to sell it.
The use of paraquat has expanded “pretty dramatically” over the last 20 years, partly because glyphosate — the active ingredient in Monsanto’s weedkiller Roundup — has become less effective, so more farmers are using paraquat again to control weeds, Gillam said.
Meanwhile, the prevalence of Parkinson’s has more than doubled from 1990 to 2015, and is expected to continue to expand rapidly, she noted.
Nearly 90,000 Americans are diagnosed with Parkinson’s every year, according to the most recent count, and the Centers for Disease Control and Prevention in 2017 ranked it among the top 15 causes of death in the U.S.
“It’s a terrible and tragic disease,” Gillam said.
Farmers who professionally apply paraquat — more than regular consumers — are the most vulnerable to the long-term health risks, Gillam said.
A familiar playbook
Kennedy and Gillam discussed the “playbook” of obfuscation tactics used by the chemical companies in the 1970s to “mislead the public and mislead regulators” about the evidence of paraquat’s effects on the brain.
Gillam said company toxicologists who knew in 1975 about the chemical’s possible chronic effects internally discussed how a “plan” could be made to conduct a study that would counter all the information that was coming out.
Kennedy said he had seen similar tactics by other chemical companies, including Monsanto. They “hire a class of scientists — we call them biostitutes — who will gin up or ghostwrite the studies and then pay legitimate scientists to sign them to give the imprimatur of legitimacy.”
In the case of Monsanto, Kennedy added, the scientific studies that ostensibly exonerated glyphosate were “ginned up by corrupted regulators.”
It’s the same playbook, said Gillam:
“You see them put up a website that puts out information that is contradictory to what they’re saying internally to each other.
“You see them talk about, ‘We need to enlist academics around the world. We can provide some funding for them. We can collaborate with them and they can carry out our positive message that our product doesn’t cause Parkinson’s disease.’”
“It’s really yet just another example of how frail our regulatory system is and how it misses these real dangers to human health,” Gillam said, “when they rely so heavily on companies to communicate the science to them.”
Suzanne Burdick, Ph.D., is a reporter and researcher for The Defender based in Fairfield, Iowa. She holds a Ph.D. in Communication Studies from the University of Texas at Austin (2021), and a master’s degree in communication and leadership from Gonzaga University (2015). Her scholarship has been published in Health Communication.
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.
January 22, 2023 Posted by aletho | Timeless or most popular | Paraquat, United States | Leave a comment
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What Is Peanut Allergy?
An Essay on the Injection That Created the Epidemic
Lies are Unbekoming | August 8, 2026
… In 1988, Japanese pediatricians began seeing something new. Children who had received the recently reformulated DTaP vaccine at three months of age were arriving at emergency rooms with anaphylaxis after eating yogurt or Jell-O. Others were reacting at their MMR shot months later. The reactions had not existed at that scale before. The pediatricians investigated. They identified the cause.
The aluminum adjuvant in the new acellular DTaP had sensitized the children to the trace gelatin proteins in the vaccine. Weeks or months later, the MMR (which also contained gelatin) delivered the second dose. The second injection provoked anaphylaxis in a subset of children. Some then reacted to gelatin in food.
The Japanese doctors wrote it down. They published. They removed gelatin from DTaP. New cases of gelatin allergy in Japanese children dropped.
The paper is on file. The cause is named. The solution worked. No Western regulator has applied the same investigation to peanut allergy, though peanut anaphylaxis emerged in Western children during the same window, at the same ages, following the same category of injection schedule change.
The Mayo Clinic’s public description of peanut allergy states that it occurs when the immune system “mistakenly identifies peanut proteins as something harmful.” FARE, the establishment’s own advocacy organization, documents that peanut allergy in US children more than tripled between 1997 and 2008. Neither statement explains why the mistake began, at scale, in a specific decade, in a specific set of countries.
The mistake framing is the tell. A mechanism that “mistakes” a food protein for a threat cannot explain why the mistake was rare in 1980 and epidemic by 1995. The body’s design did not change in fifteen years. What changed was what was injected into infants: what compounds, at what ages, in what combinations.
The Japanese case is the counterfactual. The cause was found and the epidemic was ended. What separates the Japanese gelatin admission from the Western peanut silence is not the science. The science has been in the record since 1913. What separates them is the willingness to name what was done. … Read full essay
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