The HighWire

🚨 LIVE NOW | EP 484: Monsanto scores a major glyphosate win at the Supreme Court. @AaronSiriSG joins Del on what it could mean for your food supply, plus @JeffereyJaxen on AI falling short, and @DrAndyWakefield’s new novel, “The Bequest.” x.com/i/broadcasts/1…

MAHA started as a political moment, but @peteevanschefx has always known it was something bigger. For most of human evolutionary history, food was a top priority. Somewhere in the last 50 to 60 years it slipped down the ladder. The MAHA Cookbook is his attempt to bring it back up. Evans was canceled, dropped from television, had his Facebook page permanently deleted, and was publicly mocked for talking about gut health, questioning pharmaceutical companies, and telling people to look outside the system. He knew there would be repercussions and kept going anyway. Many doctors he has interviewed believe 80% of chronic illness can be completely eradicated through lifestyle choices, and the greatest lifestyle choice, he says, is good diet. The cookbook covers what MAHA actually means, how to shop, how to clean out your pantry, ancestral diets, meal prep for fussy eaters, gut health and fermented foods, and regenerative farming practices, before getting into MAHA recipes built around real food: good quality meat, seafood, vegetables, fruit, and eggs, lower carbohydrates, and healthy fats. In the kitchen, he made three dishes in under an hour: hasselback sweet potatoes roasted in beef tallow with a fresh herb salmoriglio, a Meatzza, ground meat seasoned and cooked like a pizza base, topped with tomato, buffalo mozzarella, and heirloom tomatoes, and pears poached in coconut water with star anise, cinnamon, and ginger. Ten minutes of preparation across all three. "Food is medicine." The MAHA Cookbook is out now wherever books are sold. Full segment below 👇

Since 2001, the United States has lost more veterans to suicide than to combat. More than 6,000 die by suicide every year. A ProPublica analysis of 313 VA inspector general studies found repeated, sometimes fatal failures in behavioral care. For decades, the only tools available were pharmaceutical interventions whose harms were hidden, and millions of Americans with conditions that don't respond to those treatments have been left with nowhere to turn. President Trump signed an executive order directing HHS to accelerate research and access to psychedelic therapies, including ibogaine, psilocybin, and methylone. The FDA is issuing national priority vouchers to three companies and has allowed the first-ever clinical study of noribogaine hydrochloride to move forward in the United States. The scientific community's exploration of these therapies was shut down by political maneuvering in the early 1970s when the Controlled Substances Act lumped psilocybin and LSD with heroin and cocaine. Decades of promising research were sidelined. That work is now being picked back up. The studies are unlike anything coming out of pharmaceutical drug trials. A single treatment of Mystic, the ibogaine-magnesium protocol developed for special operations veterans with traumatic brain injuries and repeated blast combat exposures, produced remarkable reductions in PTSD, depression, and anxiety with large effect sizes, and the benefits held at the one-month follow-up. Every participant in that trial had to travel to Mexico to receive it. A BMJ meta-analysis found that psilocybin was nearly three times more likely than placebo to produce full remission of depression. A woman with advanced Alzheimer's who had been largely reduced to single words for five years received a single dose of psilocybin and within 19 hours began speaking spontaneously, recognizing family members, walking independently, and dressing herself. The grassroots fought for this for decades. The government is finally listening. Full segment below 👇

Hello, HighWire audience! We need your help! Next week on the show, we will be hosting an expert panel on peptides, and we want your questions, thoughts, comments, and experiences about them! What do YOU want to know about peptides? Have experience with them, good or bad? Comment below so we can bring your thoughts to Del for discussion with the panel!

Every major media outlet has the same message: sunscreen prevents skin cancer, wear it every day, and there is no safe tan. The HighWire went looking for the science behind that claim and found a more complicated picture. In 2019, the FDA proposed a full safety review of sunscreen ingredients. That review has still not been completed. In the meantime, an FDA-funded randomized clinical trial published in JAMA in 2020 found that all six tested active chemical sunscreen ingredients were absorbed into the bloodstream, with plasma concentrations exceeding the FDA's own threshold for requiring additional safety studies. Those elevated concentrations weren't just there after the application; they persisted for days. The Environmental Working Group's analysis of those same ingredients found strong evidence of hormone disruption and skin allergies in several of them. Only two ingredients, zinc oxide and titanium dioxide, do not absorb through the skin. They are the mineral-based options. The sun itself tells a different story than the one we are being barraged with. A systemic review of epidemiological studies found that chronic sun exposure is associated with reduced risk of colorectal, breast, prostate cancer, and non-Hodgkin's lymphoma. A Swedish cohort study found that all-cause mortality was approximately twice as high among people who avoided sun exposure compared to those with the highest sun exposure. A large UK study published earlier this year found that higher UV exposure was associated with lower all-cause, cardiovascular, and non-skin cancer mortality, and concluded that sunlight's benefits cannot be fully replaced by vitamin D supplements. The relationship between sun exposure and melanoma is also not straightforward. People who work outdoors with high chronic sun exposure have lower melanoma rates than people who work in offices. Burning is clearly harmful. But the blanket message that sun exposure causes cancer and sunscreen prevents it doesn't seem to hold up... Full segment below 👇

"There's no way this can be it" Federal regulations require vaccine package inserts to summarize the clinical trial relied upon to license the product for safety. Here is what the Recombivax HB package insert says in that section. "In three clinical studies, 434 doses of Recombivax HB were administered to 147 healthy infants and children up to 10 years of age who were monitored for five days after each dose." There was no control group, five days of safety monitoring, and 147 infants in the trial. That's the data the FDA accepted to license this product for administration to millions of babies. @AaronSiriSG couldn't believe it, and neither could we.

Aaron Siri recently reflected on what it meant to stand on the stage at the Kennedy Center and talk about vaccine safety to a room that included senior officials from the FDA, CDC, and other agencies, along with a crowd of reporters. He didn't know it was a bucket list item until the opportunity came up. When it did, he recognized exactly what it was: a chance to speak directly to the people who had gotten it so wrong and tell them what he thought they needed to do to correct course, including a lot of them firing themselves. (🤣)

Canada's Special Joint Committee on Medical Assistance in Dying has recommended indefinitely excluding patients whose sole underlying condition is mental illness from eligibility for state euthanasia. The problem the committee couldn't get past: suicidal ideation is itself a symptom of mental illness, which means a psychiatrist approving a MAID request and a psychiatrist preventing a suicide can be looking at the same patient presenting the same symptoms. "We may not be responding to an autonomous, enduring request for assisted dying, but rather to the voice of the illness itself." A 2017 study found MAID could reduce Canadian healthcare spending by up to $138.8 million annually. That number is in the same report as the ethical concerns. The full article by @smiddendorp22 who has been following this story closely for us is linked below 👇 bit.ly/mental-illness…

"There's a reason that people have an issue with vaccines. Not because they just woke up one day and decided they just wanted for fun to take a position that might get them called an antivaxer, a quack, anti-science, get their kids out of school, get them thrown out of their jobs, have them turned against their social circles, have their kids excluded from playdates. Who does that? When you abandon those people who trusted the system, that's what breeds distrust. I agree. We need to get vaccines out of politics. It should be purely medical. And the only way to do that — end mandates. By mandating a vaccine, you make it political. By using the argument that a vaccine is safe and effective to take away somebody's civil individual rights, you made the safety and efficacy of that product a legal and a political issue. And chronic disease, you want to do that, you got to address vaccines. That's the truth. Because if you look at the weight of the current available data, the weight of that science reflects that you better address vaccines if you're going to truly achieve the objectives that MAHA has. Mandates are the tool of bullies, criminals, and dictators. If a patient refuses a medical product after being conveyed its benefits and risks, then that is called informed consent. They were informed and did not consent. Mandating over this objection is immoral and illiberal." -- @AaronSiriSG

London Gadd was 12 years old. She played soccer, loved to read, drew constantly, and dreamed of flying for the Air Force. She is gone, and every parent needs to read this. Within 12 hours of admission to a psychiatric facility, a psychiatrist pushed Prozac. Her mother refused for three days. The facility told her London couldn't be released without it. A consent form later surfaced bearing her signature on a line marked for verbal consent, a document she says she never saw. London's dose was later doubled without her mother's knowledge. Injections of Zyprexa, an antipsychotic, were administered without her mother ever being told. Genetic variants that affected how London's body metabolized Prozac existed and could have been identified before discharge. No one tested for them. Pharmacogenomic testing for exactly this purpose has existed since 2006. Twenty-one days after discharge, London reached out for help. The adults who received her messages went back to sleep. She died the following day. Her mother Charay is now fighting for London's Law, which would require documented non-drug intervention before prescribing psychiatric medication to a minor, mandatory pharmacogenomic testing before any prescription, and real informed consent including the FDA's black box warning in plain language. "London paid the price for a system that labels first and investigates last." @ChelleWards and @tracybeanz wrote this one. It is not easy to read. Read it anyway. And pray for London's family. bit.ly/London-Gadd

Attorney @AaronSiriSG laid out what genuine HHS reform would actually look like. Public servants who want to work in government should commit to never entering the revolving door to industry afterward. All health data should be made public in de-identified form, and any study where that data remains hidden should be retracted for violating basic scientific method. Study protocols should be posted before funding is approved, and results should be published no matter what they show. On liability: the 1986 Act and the PREP Act immunities could be lifted by the HHS Secretary tonight with a stroke of a pen. "Secretary Kennedy could do that tonight with a stroke of a pen, but I don't think the White House would let him..."

This Thursday on The HighWire! The Supreme Court just handed glyphosate liability protection, and Aaron Siri is breaking down exactly what that means for the future of your food supply. The chemical industry can now kill, maim, and injure you and your children with effectively no legal consequence. Del has a solution: he's growing his own, and he's got tomatoes to prove it. Jefferey Jaxen joins to discuss the Ford plant rehiring the engineers it replaced with robots, and what that says about the limits of automation. And Dr. Andrew Wakefield sits down in-studio to talk about his new novel, “The Bequest,” the story of a family crossing the Oregon Trail with a child with autism, and whether it might one day become a film. The HighWire, this Thursday at 11 AM Pacific, 2 PM Eastern. 👇 The HighWire with Del Bigtree 📅 July 9, 2026 ⏰ Thursday, 11 AM PT | 2 PM ET 📺 Watch at: TheHighWire.com/WATCH

UV Lights And Laser Weed Zappers Offer Chemical-Free Alternative To Toxic Pesticides American farms are running robots through their fields overnight to eliminate the need for chemical pesticides and herbicides, and the early results are striking. UV-C light robots are delivering a 70% reduction in pesticide use on strawberry farms, with some trials reporting 90% control of mites and fungi. AI-powered laser weeders from Carbon Robotics can target and destroy hundreds of thousands of weeds per hour with precision cameras and deep-learning models, with trials showing effectiveness equal to or better than standard herbicides. The United States uses over 1 billion pounds of pesticides annually, with glyphosate-based herbicides accounting for the vast majority. The Trump administration filed a Supreme Court brief backing Bayer and signed an executive order to increase domestic glyphosate production. RFK Jr. has been publicly championing this technology as the off-ramp. "We got to get off this stuff, we got to give these farmers an off-ramp so that they can get off it. There are all these kinds of new exciting technologies that give us a light at the end of the tunnel to transition. And it could be very, very fast." Full article by @smiddendorp22 linked below 👇 bit.ly/UV-pesticide-a…

During the 2025 pertussis outbreak in West Virginia, health authorities used the surge to coerce vaccination and refuse medical exemptions, blaming the unvaccinated. ICAN filed legal demands for the actual data. In West Virginia, 71% of pertussis cases were in individuals who were fully up to date on their vaccines. Looking back across seven years of cases, 68% were vaccinated. In New York's measles outbreak, 33% of cases had received at least one dose of the MMR vaccine, with another 28% listed as unknown vaccination status. The narrative and the data are not telling the same story.

How about the claim that vaccines prevented millions of childhood illnesses? A report claims that between 1994 and 2023, routine childhood vaccination prevented 508 million cases of illness, 32 million hospitalizations, and 1.1 million deaths in the United States. @AaronSiriSG looked at how they got there. The report's own authors admit they ignored every confounding factor, including hygiene, clean water, sanitation, antibiotics, and acute care, stating those contributions "have not been incorporated into the model." That's not how modeling works. You're supposed to account for confounders, not discard them. The diphtheria numbers illustrate the problem. The report credits the vaccine with saving 25,000 lives annually, accounting for 750,000 of the 1.1 million total. But in 1948, the year before the diphtheria vaccine came into routine use, there were 634 diphtheria deaths in the United States, not 25,000. Mortality was already collapsing on its own, and in the years the vaccine was being adopted, regions that used it and regions that didn't showed identical declines. Scarlet fever never got a vaccine. It also disappeared. Nobody is running public relations campaigns about it.

💉Not a single routine injected childhood vaccine on the CDC schedule has ever been licensed based on a placebo-controlled trial. When another vaccine was used as the control, that vaccine was also never licensed based on a placebo-controlled trial. Every product on the schedule traces back through a chain of vaccines-used-as-controls, and at the bottom of that chain, there is no placebo. Aaron Siri spent ten years fighting the FDA for the clinical trial documents that prove it, and every one of them is cited in chapter 10 of "Vaccines, Amen." "That is a categorical fact. And for any reporters out there, instead of calling Paul Offit when you run out of here, why don't you actually go to chapter 10 and look at the underlying FDA licensure documents that we spent 10 years clawing out of FDA's hands for yourselves."

🚨The next frontier in virus elimination isn't targeting the virus. It's targeting you. Bill Gates has committed $200 million to Anthropic over four years and joined a separate $500 million initiative called Intercept, backed by Anthropic, OpenAI, and Stripe, with the stated goal of eliminating respiratory viruses including the common cold, influenza, and coronaviruses through new vaccines, nasal drops, pills, and air-cleaning technologies. The project is targeting 60% population uptake across all age groups regardless of individual health status. One of the core approaches being explored is host-directed antivirals, therapies that don't target the virus itself but the human proteins the virus uses to replicate. Those proteins don't exist only to help viruses. They are proteins the body uses normally, throughout the liver, kidney, brain, and immune system. A 2015 researcher studying similar therapies warned that inhibiting them broadly carries serious risk of immunosuppression and systemic side effects. Full article linked below 👇 bit.ly/gates-ai-vacci…

@nikitabier Hello, Nikita! We post native video clips of our weekly show (that is also streamed here on @X). Would we need to use the video editor for the app to recognize that we are posting original video content?

I’m going to answer this claim that “X is turning into TikTok” one time only: • Posts containing videos already make up close to half the impressions on X • Many videos from top accounts are simply stolen from other users, sometimes 5 years after they originally went viral. • Our team believes this recycled content has a negative impact on the user experience and the business. • For the first time, we are providing a functional video editor so some videos on X can finally be original content that doesn’t exist on other platforms If you are a creator that does not recycle other people’s content, you have the biggest arbitrage opportunity of your career to build an audience here. The algorithm may take time to recognize you, but when it does, you will climb faster than other account on this app.

🚨@ICANdecide Obtains Records Showing Large Numbers of Pertussis and Measles Cases Among the Vaccinated During the 2025 pertussis outbreak in West Virginia, health authorities used the surge to coerce vaccination and refuse medical exemptions, blaming the unvaccinated. ICAN filed legal demands for the actual data. In West Virginia, 71% of pertussis cases were in individuals who were fully up to date on their vaccines. Looking back across seven years of cases, 68% were vaccinated. In New York's measles outbreak, 33% of cases had received at least one dose of the MMR vaccine, with another 28% listed as unknown vaccination status. The narrative and the data are not telling the same story. Full article linked below - and please consider supporting @ICANdecide so this work can continue! 👇 bit.ly/MeaselsinVacci…

Prevnar 7 was licensed for infants at two, four, and six months of age with no placebo-controlled trial. There was no ethical reason to skip one. Instead, the control used in the clinical trial was another experimental vaccine, an investigational meningococcal conjugate vaccine that had never been licensed either. A JAMA article authored by FDA scientists acknowledged this approach can mask serious adverse events. Prevnar 7 then became the control used to license Prevnar 13. In that trial, serious adverse events including death, hospitalization, and permanent disability were reported in 8.2% of Prevnar 13 recipients and 7.2% of Prevnar 7 recipients. Prevnar 13 then became the control used to license Prevnar 15. Serious adverse events were reported in 9.6% of Prevnar 15 recipients and 8.9% of Prevnar 13 recipients. The FDA called it safe. Each generation of this vaccine was tested against the last one, and the last one was never tested against a true placebo. @AaronSiriSG calls it a pyramid scheme of safety, with a baseline that has never been shown to be safe at all.