Flashlights

Flashlights Podcast
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  1. -1 J

    Does Shedding Kill? Correlations Between Injected Teens and Adult Female Mortality | Hervé Seligmann

    "What you see is the more children 10 to 14 were injected, the more women died of cancers overall in 2021 compared to the previous year." Hervé Seligmann This is my second interview with biologist Dr. Hervé Seligmann. He has held academic positions at Aix-Marseille University, University of Oslo, Louisiana State University, the University of Chicago, and the Hebrew University of Jerusalem. *** Strong Positive Correlations between Teenage Vaccination Rates and Increased Death Rates in Adult Females About a year ago, Seligmann discovered the University of Washington's Global Health Data Exchange (GHDx). This database, maintained by the University's Institute for Health Metrics and Evaluation (IHME), contains the world's most comprehensive health and demographic data from 1980 to the present. Seligmann said: "For around 200 countries and around 200 or more diseases, they give you the death rates and the yearly incidences of all of these diseases for each country and also by sex and by age classes." When Seligmann discovered this rich data depository in early spring 2025, data were available only until 2021. He found that strange but was nonetheless happy to have at least data for 2020 and 2021. He downloaded the death rates for 2020 and 2021 from 26 countries for about 60 types of diseases - cancers as well as cardiovascular, neurological and gastroenterological diseases - and he also downloaded the injection rates cumulated over the previous month up to mid 2021 for each of the age classes provided. Then he checked for correlations and found strong positive ones between teenage vaccination rates, in particular for ages 10 to 14, and increased death rates from almost all cancer and disease types in adult females - with virtually no such correlation in adult males. CHAPTERS 0:00:04 – Intro and Herve Seligmann's background 0:02:30 – Using GHDx global health data 0:07:59 – Teen injections vs spike in female cancer deaths (2021) 0:11:30 – Interpreting the female-only signal and shedding hypothesis 0:22:30 – Data for 2020–2021 changes between spring and autumn 2025 0:27:35 – Can these updated datasets still be trusted? 0:39:56 – 2022–2023: shifting from shedding to direct injection effects 0:45:22 – "Priming" idea: injections heighten response to later shedding 0:51:31 – Ongoing boosters in older people vs dropping uptake in teens 1:07:26 – Organ-specific cancer deaths vs Pfizer biodistribution data 1:19:40 – Summary: vaccines as main driver, mechanisms remain complex RESOURCES Google Scholar - Hervé Seligmann COVID Vaccination and Age-Stratified All-Cause Mortality Risk, 2025-09-17 ScholarGPS Global Health Data Exchange, University of Washington

    1 h 29 min

  2. 22 FÉVR.

    How the FDA Lied to the American People About Covid-19 'Clinical Trials' | Sasha Latypova

    "Vaccines can reach the arms of Americans under investigational or non-investigational pathways that are separate and distinct." —Citizen Petition Regarding Covid-19 Vaccine Licensure https://flashlightsproductions.substack.com/p/how-the-fda-lied-to-the-american?utm_source=youtube This is the second part of my interview with Sasha Latypova in which we discuss the petition's arguments in detail. The petition was filed in December 2025 by Children's Health Defense to request that the FDA revoke the Biologics License Application approvals (BLAs) for the Pfizer and Moderna Covid-19 shots. Latypova wrote extensive parts of the petition. THE PETITION'S CORE LEGAL ARGUMENT Products developed under Emergency Use Authorization (EUA) cannot simply be granted Biologics License Applications (BLAs). It's like declaring sewage to be water. But the FDA retroactively granted Pfizer's and Moderna's mRNA Covid-19 vaccines full BLA approval they never legally earned. Therefore, the citizen petition argues, these products have been misbranded. Misbranding is not a minor infraction, Sasha Latypova told me, but a federal crime that can trigger seizure, injunction, criminal penalties, and license revocation. WHY IS MISBRANDING SUCH A BIG DEAL? It's a long and difficult process to obtain BLA approval from the FDA. Under section 351 of the Public Health Service Act, FDA may approve a BLA only if the vaccine is shown to be safe, pure, and potent for its intended use. In addition, it must be manufactured in facilities that consistently meet regulatory standards. Usually, it takes many years to obtain BLA approval. CHAPTERS 0:00:05 Citizen Petition Overview and Claim of Vaccine Misbranding 0:01:38 FDA's Original Mandate: Misbranding, Adulteration, Interstate Commerce 0:02:35 Federal vs State Authority and Possibility of State‑Level Divergence 0:05:04 Misbranding as a Serious Federal Crime and FDA's Dormant Powers 0:05:36 Investigational vs Non‑Investigational (EUA) Pathways 0:09:02 PREP Act Origins and Congressional Justification for EUA Countermeasures 0:13:08 No True Clinical Trials: EUA Products and "The Trial Charade" 0:14:46 Brooke Jackson's Case 0:22:59 Media Framing: "Technicalities" vs Binding Law on Labeling and Pathways 0:27:39 Core Demands of the Petition: Revoke BLAs, Re‑Designate as EUA Products 0:29:43 Informed Consent, Nuremberg Legacy, and the Missing IRB Oversight 0:32:45 EUA Products Cannot Be Mandated – Yet Mandates Were Imposed Anyway 0:34:53 EUA Suspends FDCA Safeguards: cGMP Deviations and Non‑Regulation 0:39:56 Expiration Date Extensions and the 2069 Pfizer Lot Anomaly 0:48:46 Comparing BLA Standards vs EUA: Safety, Purity, Potency, Sterility, Identity 0:54:31 Manufacturing Process Validation and Extreme Lot‑to‑Lot Variability 1:05:30 Petition's Legal Conclusion on FDA Violations

    1 h 7 min

  3. 15 FÉVR.

    Deadly Chain of Command: From Federal Bureaucrats to Hospital CFOs to Doctors | Ken McCarthy

    "When we neither punish nor reproach evildoers, we are not simply protecting their trivial old age. We are thereby ripping the foundations of justice from beneath new generations." —Alexander Solzhenitsyn, The Gulag Archipelago For the entire post, click here: https://flashlightsproductions.substack.com/p/deadly-chain-of-command-from-federal Few Americans Know About the Extent of Medical Murders During Covid This is the third and last part of my interview with Ken McCarthy, author of 'What the Nurses Saw - An Investigation Into Systemic Medical Murders That Took Place in Hospitals During the COVID Panic.' It's almost exactly six years since the start of the Covid-19 Pandemic. But way too few people in America know about the extent of the systemic medical murders that the nurses saw. His book, McCarthy told me, is a witness to the crimes that happened during the Pandemic: "If you witness a crime, if you witness somebody being abused, you're sort of obligated as a human being to try to interfere or at a minimum report it to somebody who can intervene and help. So that's the function of this book. It exists. People do read it. It's slowly moving its way through the world. And I hope more and more people become aware of it, become aware of the stories so that they can protect themselves." Medicine's Return to the Middle Ages McCarthy is convinced that medicine is firmly back in the Middle Ages. Back then, he said, there were "a lot of insane medical practices and they were validated or authorized by the ultimate authority, which happened to be the Catholic Church… We are literally back to where medicine is being authorized and promulgated [by an entity] that has nothing to do with medicine, has nothing to do with science, has nothing to do with public health. It is simply a directive from the most powerful forces in the society, which now are the federal governments." Remdesivir Approved for Prematurely Born Babies Remdesivir, one of Fauci's pet drugs, is a good example of such insane practices not rooted in science. Nurses nicknamed Remdesivir 'Run! Death Is Near.' The drug, which is known for its extreme toxicity - it leads to kidney failure among a host of other adverse events - received Emergency Use Authorization (EUA) in April 2020, followed by FDA approval in October 2020 but limited to children older than eleven years. One month later, in November 2020, the WHO advised against the use of Remdesivir for Covid-19 patients. The drug was subsequently discontinued in Europe. But not in America. Not to this day. In the United States, the drug remained under Emergency Use Authorization for children younger than 12 until spring 2022 when it received FDA approval for pediatric use for all children older than 27 days. Yes, you read that right: days. CHAPTERS 0:00:05 Remdesivir's EUA and FDA approval 0:01:30 Remdesivir for Premature Babies 0:03:14 Profits, Fauci, and federal drug royalties 0:05:27 Veklury patient marketing 0:07:22 Modern medieval medicine 0:09:19 Federal protocols & the hospital chain of command 0:13:28 Whistleblower nurses, firings, and blacklisting 0:17:57 The need for medical advocates 0:22:13 Nurse–doctor hierarchy and lost collaboration

    24 min

  4. 11 FÉVR.

    More than 250,000 Excess Renal Failure Deaths Since 2020 | John Beaudoin

    "If you're a health monitoring agency like the CDC, it's your job to look at the thing that's staring you right in the face." —John Beaudoin https://flashlightsproductions.substack.com/p/more-than-250000-excess-renal-failure?utm_source=youtube In this third and last part of my interview with John Beaudoin, we're looking at CDC's data for acute kidney or renal failure deaths from 2018 until 2025. For years, Beaudoin has been sounding the alarm about a staggering increase in acute kidney failure deaths beginning in 2020 - but he got little traction. One reason is that these deaths are not apparent when researchers exclusively use Underlying Cause of Death (UCoD) in their analysis of CDC's mortality data. CHAPTERS 0:00:05 Why Acute Renal Failure Matters Now 0:00:31 Death Certificates: Underlying vs Multiple Causes 0:01:25 Acute Renal Failure Deaths 2018–2025: The Spike 0:03:14 Excess Deaths and Life-Years Lost 0:07:20 Renal Failure vs Myocarditis: What's Bigger? 0:09:12 Young People and Acute Renal Failure 0:10:36 20-Year Trends and the Male–Female Split 0:14:22 What Could Be Driving the Renal Failure Surge? 0:17:28 Are Recording Practices Skewing the Data? 0:20:43 What This Data Can — and Cannot — Tell U

    22 min

  5. 5 FÉVR.

    Peter Thiel's 'House Philosopher' Proposes 'Humane Alternative to Genocide' | Patrick Wood

    "The ideal solution achieves the same result as mass murder (the removal of undesirable elements from society), but without any of the moral stigma." —Curtis Yarvin, 2008 https://flashlightsproductions.substack.com/p/peter-thiels-house-philosopher-proposed?utm_source=youtube "Our goal, in short, is a humane alternative to genocide. That is: the ideal solution achieves the same result as mass murder (the removal of undesirable elements from society), but without any of the moral stigma. Perfection cannot be achieved on both these counts, but we can get closer than most might think. The best humane alternative to genocide I can think of is not to liquidate the wards — either metaphorically or literally — but to virtualize them. A virtualized human is in permanent solitary confinement, waxed like a bee larva into a cell which is sealed except for emergencies. This would drive him insane, except that the cell contains an immersive virtual-reality interface which allows him to experience a rich, fulfilling life in a completely imaginary world." —Curtis Yarvin, 2008 YARVIN's VISION Why, I asked Patrick Wood during our interview about his latest book 'The Final Betrayal: How Technocracy Destroyed America'', would anyone care what Curtis Yarvin thinks?  Turns out we should care a lot since Peter Thiel regards Yarvin as his 'House Philosopher.' And Thiel is not the only one among the billionaire technocrats who has taken a liking to the philosophy of Dark Enlightenment. But does Thiel share Yarvin's vision of a 'humane alternative to genocide'? Maybe. It certainly doesn't bode well that NYT podcaster Ross Douthat had to ask him three times during an interview last year if Thiel wanted humanity to continue. H e got only silence as response until, when asked with much urgency, for a third time, Thiel relented with a 'Yes, but…' The 'but' was: let them survive - but not without some desperately needed technical enhancements inside their bodies and brains. CHAPTERS 0:00:04 – Intro, Curtis Yarvin "Humane Alternative to Genocide" Passage   0:01:41 – Who Is Curtis Yarvin? Dark Enlightenment and Silicon Valley Influence   0:08:56 – Peter Thiel's Role: Funding Yarvin, Technocracy, and Monopoly Mindset   0:14:03 – Post‑9/11 Surveillance, Total Information Awareness, and Birth of Palantir   0:17:40 – Democracy vs Freedom? Thiel, Yarvin, and Technocratic Alternatives   0:23:17 – "You Will Own Nothing and Be Happy": Virtual Bubbles and WEF‑Style Dystopia   0:30:15 – Monarch CEO, Sovereign Corporations, and the End of Private Property   0:32:48 – AI as De Facto Ruler: Centralized Data, Palantir, and Weaponized Governance   0:43:53 – Bilderberg Power: Thiel, Karp, AI Agendas, and Choosing Leaders   0:46:13 – Technocracy as an Economic System: Eliminating Politics and Politicians   0:50:43 – Trump, Technocrats in DC, and Yarvin's RAGE Doctrine (Retire All Government Employees)   0:54:22 – Marxism, Bolshevism, Nazi Germany, China: Historical Roots of Technocratic Control   1:02:11 – AI as New Religion: AI God, Thiel's Antichrist Lectures, and Inverted Theology   1:06:40 – Data Centers, Compute, and Building a Global AI Control Infrastructure   1:18:13 – Why Harvest All This Data? From Wearables and Smartphones to Total Control   1:21:32 – Politicians Behind the Curve and AI's Rapid Capture of Government   1:26:29 – Will the AI Bubble Burst? Societal Strain vs Oligarchs' Race to Finish   1:32:44 – COVID‑19, Lack of Accountability, and the Illusion of Rights in a Technocratic Order   RESOURCES Patrick Wood: The Final Betrayal: How Technocracy Destroyed America https://www.amazon.com/Final-Betrayal-Technocracy-Destroyed-America/dp/B0GD2LCBSB/ref=sr_1_1?s=books&sr=1-1 Patrick Wood's Technocracy News: https://www.technocracy.news/ Nick Land: The Dark Enlightenment https://www.amazon.com/Dark-Enlightenment-Imperium-Press/dp/192260268X/ref=sr_1_1?sr=8-1 Curtis Yarvin/Mencius Moldbug: Patchwork: A Political System for the 21st Century https://www.unqualified-reservations.org/2008/11/patchwork-2-profit-strategies-for-our/

    1 h 36 min

  6. 29 JANV.

    FDA's fraudulent BLA Approval of Pfizer's and Moderna's Covid Shots | Sasha Latypova

    Imagine the following: you wake up one morning to the news that the federal government declared sewage to be in compliance with the Safe Drinking Water Act (SDWA).  https://flashlightsproductions.substack.com/p/fdas-fraudulent-bla-approval-of-pfizers?utm_source=youtube *** It's all pretty confusing with these toxic mRNA Covid shots. At first they were under Emergency Use Authorization, then the FDA gave them BLA approval but continued to give the EUA shots for more than a year after BLA approval to most Americans. And what role does the PREP act play in all this? To quickly understand the basic concept of the BLA approval game that the FDA has played, imagine the following: you wake up one morning to the news that the federal government declared sewage to be in compliance with the Safe Drinking Water Act (SDWA). And the EPA has confirmed that sewage complies with the agency's established health-based standards for contaminants in public drinking water. You turn on your faucet. And, sure enough, sewage comes flowing out of it. If you decided to drink it, you wouldn't be able to sue the government when you get sick because sewage has been declared a medical countermeasure under the protection of the PREP act, granting freedom of liability to all municipalities, waterworks etc. in the entire country. This analogy only goes so far though: after all, before the government declared sewage to be compliant with the Safe Drinking Water Act, it didn't put sewage under some kind of Emergency Use Authorization and it didn't mandate you to drink it in order to keep your job. PS: This analogy is only meant to highlight the difference in regulatory pathways between EUA authorized and BLA licensed biologics. That's all. Because the BLA Covid shots are as toxic as the EUA shots. They served us sewage from the start. CHAPTERS 0:00:05 CHD's Citizen Petition To Revoke Pfizer And Moderna BLAs 0:05:07 Public Response And Record Comment Numbers 0:11:06 What Are Biologics? Basic FDA Categories 0:15:18 From Traditional Biologics To mRNA "Biologics" 0:21:52 NDA vs BLA And Biologics Carve‑outs 0:27:49 Biologics, Vaccines, And Industry Incentives 0:31:19 Growth Of Biologic Drugs And Vaccine Focus 0:31:41 EUA Timeline And 2021 BLA Approvals 0:33:45 Comirnaty Rollout In US vs Europe And Relabeling Claims 0:36:15 Confusion Among Public And Doctors About EUA vs BLA 0:37:28 FOIA Delays And EUA vs EAU Confusion 0:39:40 EUA As Countermeasure Outside Normal FDA Rules 0:43:42 Sewage vs Drinking Water Analogy For EUA vs BLA RESOURCES CHD's Citizen Petition: https://childrenshealthdefense.org/wp-content/uploads/FDA-2025-P-6831-0001_attachment_1.pdf Tell the FDA to Revoke Licenses on COVID Vaccines: https://childrenshealthdefense.org/community/tell-the-fda-to-revoke-licenses-on-covid-vaccines/ Sasha Latypova Breaking: Citizen Petition to the FDA filed by Children's Health Defense with my input. https://sashalatypova.substack.com/p/breaking-citizen-petition-to-the Biologics License Applications (BLA) Process (CBER): https://www.fda.gov/vaccines-blood-biologics/development-approval-process-cber/biologics-license-applications-bla-process-cber

    51 min

  7. 25 JANV.

    Vanished Study Finds Synthetic mRNA from the Pfizer Shots in Placentas of Vaccinated and Unvaccinated Women | Tom Haviland

    "The link is gone. The paper has been pulled. But there's no information about it. Nothing. It's just gone." *** https://flashlightsproductions.substack.com/p/vanished-study-finds-synthetic-mrna An Israeli study titled 'Detection of Pfizer BioNTech Messenger RNA COVID-19 Vaccine in Human Blood, Placenta and Semen' was published by Gavin Publishers mid October 2025 and made headlines in independent media. However, the paper didn't see the light of day for long. In early December it vanished. It was not retracted, it just quietly disappeared without any explanation whatsoever. After my interview with Haviland, I discovered the paper on the Wayback machine as an archived snapshot from December 5, 2025, shortly before it disappeared: https://web.archive.org/web/20251205172931/https://www.gavinpublishers.com/assets/articles_pdf/Detection-of-Pfizer-BioNTech-Messenger-RNA-COVID-19-Vaccine-in-Human-Blood-Placenta-and-Semen.pdf CHAPTERS 0:00:56 Article Removal and Initial Reactions 0:01:57 Study Overview and Israeli Vaccination Context 0:04:27 Early Findings on mRNA Persistence 0:06:37 Groundbreaking Detection in Placenta 0:07:36 Nested PCR Method Explanation 0:10:29 Sample Collection Timeline 0:12:28 Delays in Publication and Data Analysis 0:15:31 Lipid Nanoparticles and Systemic Distribution 0:18:28 Detection Rates by Time Since Vaccination 0:23:33 Shedding Hypothesis and Children's Mortality Analysis 0:27:20 Vaccination Timing and Pregnancy Outcomes 0:32:07 mRNA Presence in Male Reproductive Cells 0:36:17 Correlation of Detection with Days Since Last Dose 0:37:04 Discussion: Transplacental Transfer and Limitations 0:40:15 Unusual Fetal Deaths and Placental Issues 0:41:07 PCR Method Limitations and Need for Further Research RESOURCES 'Detection of Pfizer BioNTech Messenger RNA COVID-19 Vaccine in Human Blood, Placenta and Semen' Laura Kasner's Substack: Clotastrophe

    49 min

  8. 20 JANV.

    How America & Europe Manipulate Child Excess Mortality: Hervé Seligmann

    This is the third part of my interview with biologist Hervé Seligmann. "The structure of these biases is so complex: It's affected by age, by severity rank, it's for missing data, for publication delay. And it always goes in the same direction: hiding injury & death." - Seligmann We discuss how EuroMOMO and VAERS Hide excess deaths in children during the Covid years. CHAPTERS 0:00:05 Euromomo Data and Excess Children Mortality 0:02:31 Age Groups and Vaccine Rollout Timelines 0:03:14 Changing Data and Baseline Comparisons Over Time 0:06:09 Critique of Data Modeling and Information Confusion 0:12:10 Analysis of CDC State-Level Excess Mortality and VAERS Correlations 0:17:03 Missing Data Issues in VAERS Reports 0:20:00 Bias in Administrative Handling of Vaccine Adverse Event Reporting 0:24:30 Evidence of Hiding Severe Harms in Children's Vaccine Reporting 0:32:11 Preview of Upcoming Unpublished Results and Future Discussion RESOURCES Google Scholar - Hervé Seligmann COVID Vaccination and Age-Stratified All-Cause Mortality Risk, 2025-09-17 ScholarGPS Albert Benavides: VAERSAware EuroMOMO

    33 min
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My personal Substack

Informations

  • Créateur
    Flashlights Podcast
  • Années d’activité
    2025 - 2026
  • Épisodes
    33
  • Classement
    Tout public
  • Copyright
    © Cornelia Mrose
  • Site Web de l’émission
    Flashlights