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The HighWire

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High above the circus of mainstream media spin, death-defying talk without the corporate safety net… this is The HighWire.

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🚨 TODAY IS THE DAY! An Inconvenient Study premieres TODAY, SUNDAY, 10/12, at the Malibu Film Festival! 📽️YOU can attend! There’s still a bit of time to click the link for tickets. Use code ICAN for 10% off! 📷 WATCH the film when it releases WORLDWIDE 10/12 at 5 pm PT (8 pm ET) on our website, FREE of CHARGE, and share it everywhere! 🚀We need your help to make it go viral. Attend. Host a watch party. Share it everywhere. This could change EVERYTHING.

🚨 TODAY IS THE DAY! An Inconvenient Study premieres TODAY, SUNDAY, 10/12, at the Malibu Film Festival! 📽️YOU can attend! There’s still a bit of time to click the link for tickets. Use code ICAN for 10% off! 📷 WATCH the film when it releases WORLDWIDE 10/12 at 5 pm PT (8 pm ET) on our website, FREE of CHARGE, and share it everywhere! 🚀We need your help to make it go viral. Attend. Host a watch party. Share it everywhere. This could change EVERYTHING.

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It worked with vaccines. They're trying it again with our food supply. While everyone's eyes are on bombs dropping overseas, something just happened in Washington that will affect every American sitting down to dinner for generations. The Trump administration's EPA filed a brief at the Supreme Court backing Bayer, arguing that because the EPA never required a cancer warning label on glyphosate, Bayer can't be held liable for not putting one there either. Never mind that the only major safety study the EPA leaned on to clear the product was just retracted weeks ago for its ties to industry. Never mind that three of the nine DOJ attorneys who signed the brief previously worked for law firms that represented Bayer and Monsanto. Glyphosate is sprayed on 80 to 90% of our crops. Over $10 billion has been paid out in cancer lawsuits. 97.8% of respondents to ICAN's poll oppose liability immunity for glyphosate manufacturers. 89% oppose the federal stockpile. And 80% say the retraction of that foundational safety study has shaken their trust in current safety claims. Del has been covering this since 2015 - before the lawsuits, before the WHO declared glyphosate a probable carcinogen, before any of this was mainstream. He saw exactly where it was heading. This is the same playbook as 1986. Get the government to grant immunity. Remove market forces. Remove the ability to sue. And then nobody has any reason to make a better product ever again. It worked with vaccines. They're trying it again with our food supply. April 27th. Washington DC. Supreme Court steps. The People vs. Poison. Mark it. Be there.

The HighWire

262,545 views • 5 months ago

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The FDA has approved Moderna's mRNA flu vaccine, the first flu shot using mRNA technology to reach the US market. The approval comes months after the same agency refused to even file Moderna's original application. Vinay Prasad, who took over the FDA's biologics division after Peter Marks, rejected the initial application in writing, citing the trial as not adequate and well controlled. His internal memo to FDA staff, later leaked to the Washington Post, called the annual flu vaccine framework an evidence-based catastrophe of low quality evidence, poor surrogate assays, and uncertain effectiveness measured with poor methods. Twelve former FDA chiefs responded by blasting his move to tighten vaccine standards in the New England Journal of Medicine. Prasad has since left the agency. ICAN submitted a letter to the FDA's independent VRBPAC committee before the vote laying out the problems: the vaccine was compared not against placebo but against a GSK product that Prasad himself called not best in class, the absolute influenza risk reduction was only 0.8% while the adverse reaction profile ran at 6.4%, the trial used a single season of data, and Part A of the trial produced more patient deaths than the comparator flu shot. The committee approved it anyway. Del Bigtree and Jefferey Jaxen walk through why this matters beyond the flu shot itself: mRNA technology, justified under COVID emergency conditions, is now entering the routine recommended schedule through a non-emergency approval, and will be the first mRNA product included in the vaccine injury compensation table. The flu shot is currently approved for adults 50 and older, fast-tracked for 65 and older.

The HighWire

18,826 views • 11 days ago

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Ghislaine Maxwell's father, Robert Maxwell, built the for-profit peer-reviewed scientific journal system that has controlled what counts as "settled science" for decades. Scientists had to publish through it. Universities were forced to buy it at inflated prices. He sat at the top and collected the profits. That's the family tree. Now the Epstein files are filling in the rest of the picture. Bill Gates invested $10 million in ResearchGate - a 25-million-member science publishing platform. Gates' chief science and technology advisor, Dr. Boris Nikolic, was feeding Jeffrey Epstein real-time insider updates on the investment. Email after email. Progress reports. Funding round timelines. Hyping the platform's growing influence over what research gets amplified and what quietly disappears. Why would a sex trafficker care about a science publishing platform? Whoever controls the feeds and recommendations controls what research gets spotlighted, what projects get grants, and what the public is told is solid science. Epstein and the people around him weren't just collecting compromising information on powerful people. They were building an operational infrastructure to monopolize science, medicine, and narrative control. Gates first denied the Russian affairs in the files. Then admitted them. The limited hangout isn't working. And as this segment was going to air, the president of the World Economic Forum resigned over his ties to Epstein. The dominoes keep falling. And we keep watching. Jefferey Jaxen Full episode at

The HighWire

199,635 views • 6 months ago