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No, Futurism, One Momentary Hot Spot on Antarctica Doesn’t Prove a Climate Crisis

By Anthony Watts | ClimateRealism | June 23, 2026

A recent article in the online journal Futurism, titled, “Scientists Horrified as Huge Heatwave Hits Antarctica,” claims climate change caused a “huge heatwave” in Antarctica, bringing temperatures on the Antarctic Peninsula nearly 36°F above average and briefly pushing readings above freezing. This is highly misleading. A single weather event says nothing meaningful about long-term climate trends, and the article ignores both Antarctica’s enormous geographic variability and the exceptionally cold conditions simultaneously occurring elsewhere on the continent. The heatwave Futurism suggested wasn’t a continent-wide crisis, but was a localized, unalarming event.

The article is largely a rewrite of a Guardian story focused on temperatures measured on the Trinity Peninsula, the northernmost extension of Antarctica. Researchers reported temperatures reaching approximately 15.4°C (59.7°F) during a brief warm spell on June 6.

What readers are not told is that the Antarctic Peninsula is not representative of Antarctica as a whole.

In fact, the warmest part of Antarctica is the Antarctic Peninsula. Nicknamed the “banana belt,” it stretches northward toward South America and experiences milder maritime conditions. During the austral summer, temperatures can occasionally exceed 10°C (50°F). The peninsula extends northward toward South America and is heavily influenced by maritime weather patterns and ocean currents. It is by far the warmest part of Antarctica and has long experienced periodic warm-air intrusions, föhn wind events, rain episodes, and above-freezing temperatures. These events are unusual, but they are not unprecedented.

In fact, the article itself acknowledges that the warmth was associated with “extremely strong westerlies.” In other words, this was a weather event driven by warmer atmospheric circulation patterns, not a direct measurement of climate change.

What Futurism misses is the fact that weather is not climate.

Climate is measured over decades. A single day, a single week, or even a single season tells us very little about long-term temperature trends. If every unusually warm day is presented as proof of climate catastrophe, then intellectual consistency would require every unusually cold day to be presented as evidence against it. The media rarely applies that standard.

The timing of this story is especially revealing because while headlines were breathlessly reporting a temporary warm spell on the Antarctic Peninsula, much of the rest of Antarctica was experiencing brutally cold conditions.

According to observations highlighted by meteorologist Cap Allon, the Amundsen-Scott South Pole Station recorded a temperature of -73.6°C (-100.5°F) on June 16, with a daily maximum of only -69.9°C (-93.8°F). That was the South Pole’s first sub–70°C reading since 2023.

One part of Antarctica briefly experiences an unusual warm episode, while another part of the continent drops below -100°F. That is how weather works on a continent larger than the United States and Mexico combined.

Yet only one of those events, specifically the anomalous high temperature one, generated international headlines.

The article further claims that the heatwave follows “decades of increasingly warm temperatures observed on the white continent.” That statement is false.

Antarctica is not warming uniformly. While portions of the Antarctic Peninsula experienced warming during parts of the late twentieth century, numerous studies have shown little warming or even cooling across large sections of East Antarctica, with East Antarctica making up the bulk of the continent. Antarctic sea ice has also exhibited substantial variability from year to year and decade to decade.

The continent is governed by complex interactions involving ocean currents, atmospheric circulation, volcanic influences (including subsurface heating under West Antarctica where the peninsula lies), sea ice dynamics, and natural climate oscillations. That complexity disappears in Futurism’s opinionated article.

Instead, readers are given the now-familiar formula: identify a dramatic weather event, attach it to climate change, mention the “Doomsday Glacier,” and imply catastrophe is around the corner. Climate Realism has debunked claims of the Thwaites Glacier’s imminent collapse repeatedly, previously. The article’s reference to Thwaites Glacier is a particularly misleading red herring, because it has nothing to do with the reported weather event. The mention serves one purpose: reinforcing a broader climate crisis narrative.

This is increasingly common in climate reporting. Any unusual weather event becomes an opportunity to recycle the same talking points about glaciers, sea level rise, tipping points, and future disasters, regardless of whether they are directly related to the event being discussed.

Concerning the Antarctic Peninsula, the facts are these: Antarctica has always been susceptible to periodic warm-air intrusions because of its geography and proximity to relatively warmer ocean waters; the Southern Ocean, atmospheric rivers, and strong westerly winds can occasionally transport substantial heat into the region. These processes existed long before climate change became a political issue.

Most importantly, a single warm event cannot establish a trend. Scientists understand this principle when analyzing climate data. Journalists should understand it as well.

A proper climate analysis requires decades of observations across the continent, careful examination of regional variability, and separation of weather noise from climate signals, not the slap dash presentation of misleading, sensational claims assembled by Futurism.

Antarctica remains the coldest continent on Earth. While the Antarctic Peninsula briefly experienced unusually mild conditions, the South Pole itself was simultaneously plunging near or below -100°F in multiple other locations.

That fact alone should remind readers that one weather event, no matter how dramatic the headline, is not evidence of a “climate emergency,” it’s simply weather. One warm spell on the Antarctic Peninsula becomes proof of climate catastrophe, while simultaneous temperatures below -100°F at the South Pole are ignored. That’s not objective journalism, that’s agenda-driven alarmism.

July 5, 2026 Posted by | Deception, Science and Pseudo-Science | Comments Off on No, Futurism, One Momentary Hot Spot on Antarctica Doesn’t Prove a Climate Crisis

Survivorship Bias: The Logical Error at the Heart of Modern Medicine

An Essay on Why You Only Hear From the People Who Lived

Lies are Unbekoming | June 18, 2026

The bullet holes show where a plane could be hit and survive. The places without holes are where the lost planes were hit.
Illustration: Martin Grandjean, McGeddon, and Cameron Moll. Wikimedia Commons, CC BY-SA 4.0. Source: File:Survivorship-bias.svg

Wald at the Statistical Research Group

In 1943, the U.S. military was about to armor its bombers in exactly the wrong places. The analysts had examined every bomber that came back from combat, mapped the bullet holes across the airframe, and proposed reinforcing the spots where the holes clustered. The data was right there. You could see it on the planes.

They referred the question to the Statistical Research Group at Columbia University, a small team of mathematicians assembled for the war effort. The Hungarian-born statistician Abraham Wald examined the bullet-hole maps and gave the opposite recommendation. Armor the engines and the cockpit. The places where the returning planes had no bullet holes.

The military analysts had committed a logical error so simple they could not see it. They were studying the planes that came back. The planes shot through the engines and the cockpit did not come back. They had gone down across two oceans and the territory between them. The returning planes did not reveal where bombers were vulnerable. They revealed where bombers could be hit and still fly home.

The bullet holes on the survivors mapped survivable damage, not dangerous damage. Armoring where the holes were meant armoring the places that did not need armoring. The damage that mattered was on the planes you could not examine because they were destroyed.

Wald’s memorandum was classified. Decades later, when his work was declassified and republished, the principle he had identified came to be called survivorship bias.¹ ² It is the most pervasive and least understood logical error in any field that draws conclusions from a visible population of survivors.

The same error sits at the center of the modern screening-and-treatment industry.

The Error Generalized

Survivorship bias operates wherever a process selects what gets seen. The destroyed do not file reports, and the audience reads only what made it through.

Mutual fund performance averages exclude funds that closed. Hedge fund return statistics quietly drop the funds that liquidated. The historical returns of “the market” routinely omit bankruptcies, delistings, and total losses. Funds that lived publish their numbers; funds that died publish nothing. The retail investor reads the winners.

The literature on entrepreneurship was built the same way. CEOs who succeeded wrote memoirs about their habits and their early-morning routines. The thousands of equally disciplined founders who failed wrote nothing because their companies went under. The “success habits” identified by reading the survivors are, in many cases, just habits, shared by the dead and the living alike, with no causal relationship to outcomes.

In architecture, the buildings that survive are studied for their construction methods. The buildings that collapsed in storms, earthquakes, or fires are no longer there to be examined. Old buildings appear well-built because the badly-built ones are gone.

In each case, the visible sample is selected by the very property you are trying to measure. You cannot learn about plane vulnerability from intact planes. You cannot learn about cancer survival from cancer survivors.

Survivorship Bias in Medicine

A woman undergoes mammography in her early fifties. The scan finds a small lesion. She receives a biopsy, a lumpectomy, six weeks of radiation, and five years of tamoxifen. She is alive ten years later. She becomes an advocate, walking in Race for the Cure and telling her sister, her daughter, and the women in her neighborhood that screening saved her life. Get the test.

Her experience is real, her gratitude genuine. The conclusion she draws does not follow from either.

What she does not know, what she cannot know, is what would have happened to her without the screening, the biopsy, the surgery, the radiation, and the years of medication. She cannot run the counterfactual on herself. The version of her that did not get the treatment does not exist, and she has no way to consult it.

The institutions that promoted her screening have access to data she does not. Population-level data, accumulated across decades of randomized and observational studies, is consistent with four overlapping forms of survivorship bias, each of which inflates the apparent success of the system. Together they are sufficient to explain most of what the industry presents as the triumph of “early detection.”

Survivorship Bias Proper

The most direct form: only the living testify.

Eight months after her mastectomy, a woman dies of chemotherapy-induced sepsis. She does not appear at the October fundraiser. Six weeks after his prostatectomy, a man dies of cardiac complications. He writes no op-eds about prostate health. The radiation that “cured” the first cancer induces a second one five years later, and the patient’s family attends a funeral, not a marathon. The chemotherapy regimen that ostensibly drove the tumor into remission also drove the patient’s bone marrow into failure, and she dies of sepsis a year later, recorded by quiet bureaucratic convention as a “cancer death.”

When the public hears about cancer treatment, it hears from the patients who survived. Those who did not survive are statistically invisible. They are counted in mortality columns nobody reads, while their grateful surviving counterparts address the television cameras. The audience for screening campaigns sees a heavily filtered population, filtered by the treatments themselves.

The filtering goes further than visibility. It reaches into the mortality data itself. When a patient on chemotherapy dies of cardiotoxic heart failure, the death is typically coded as a cancer death. When a patient with treatment-induced bone marrow failure dies of sepsis, it is coded as a cancer death. When the surgical complication kills the patient on the operating table, it is generally coded as a cancer death. When the second cancer induced by radiation given for the first cancer kills the patient ten years later, the second cancer is frequently recorded as primary, the radiation that caused it noted in passing if at all. The coding conventions tilt systematically in one direction: failures of treatment are folded back into the column labeled “disease.” The treatment is shielded from blame. The cancer absorbs it. The mortality statistics that institutions cite to justify aggressive treatment are themselves an artifact of how treatment failures are recorded.

Lead-Time Bias

Finding a cancer earlier does not mean treating it earlier extends life. It means knowing about it longer.

Two women with identical lesions, identical biology, and identical eventual outcomes. Both die at age seventy. Woman A is screened at fifty, her cancer is detected, and she is “treated” for the next twenty years. Woman B is unscreened. She develops symptoms at sixty-five, is diagnosed, and dies at seventy.

The standard reporting metric is five-year survival from diagnosis. By that measure, Woman A counts at 100% survival. Woman B counts at 0%. The treatment looks miraculous. Nothing has actually changed. Both women died at seventy. Woman A simply spent twenty years as a patient.

The five-year survival statistic is the standard currency of cancer reporting. In the presence of widespread screening, it is also a metric that can rise to 100% without saving a single life. Between 1950 and 1995, the five-year survival rate for prostate cancer in the United States rose from 43% to 93%. The age-adjusted mortality rate from prostate cancer over the same period barely moved.³ The screened population learned about their cancer earlier. They did not die later.

When you read that “early detection” has improved five-year survival rates for breast, prostate, or thyroid cancer, you are reading a statistic structurally biased toward the appearance of benefit even when no benefit exists.³ ⁴

Length-Time Bias

Screening preferentially detects slow-growing lesions. Aggressive cancers grow rapidly between screening intervals and present symptomatically, not through the scan. Indolent lesions sit for years, available to be detected at the next mammogram or PSA test.

The population of cancers caught by screening is therefore enriched for slow biology, for lesions that were less likely to kill in the first place. Patients with these lesions tend to do well, not because the screening saved them but because their cancers were not going to kill them on any rapid timescale. The aggressive cancers, the ones that genuinely threaten life, frequently arise and progress in the gaps between scans.

Screening catches the cancers least in need of catching. The system then takes credit for the favorable outcomes of patients who would have done well regardless.

Overdiagnosis

The fourth and most powerful form. Many of the lesions detected by screening are not, in any meaningful sense, going to harm the patient. They are stable, non-progressive anatomical findings that medicine has chosen to label as cancer.

Bleyer and Welch, examining three decades of U.S. mammography data, estimated that 31% of breast cancers detected by screening represented overdiagnosis: disease that would never have produced symptoms or shortened life.⁵ The Cochrane systematic review of mammography trials concluded that for every life potentially saved by screening, ten women receive treatment for a cancer that would not have harmed them. The same review found no reduction in all-cause mortality from screening.⁶

In South Korea, the introduction of widespread thyroid ultrasound produced a fifteen-fold increase in thyroid cancer diagnoses over two decades. Mortality from thyroid cancer did not change. The country had not experienced a thyroid cancer epidemic. It had begun finding microscopic lesions that had always existed in the population, at autopsy in people who died of other causes, and that had never killed anyone before they were found and treated.⁷

Autopsy studies of men who died of unrelated causes have found prostate cancer cells in roughly a third of those in their forties, rising to two-thirds by their late sixties.¹⁵ The lifetime mortality from prostate cancer is approximately 3%. Most older men carry the disease into a natural death from something else; they die with prostate cancer, not from it. The PSA test cannot distinguish between the cancer that would have killed and the cancer that would have been silently carried into the grave. It detects both. It produces a diagnosis in both. The men with non-threatening lesions, who vastly outnumber the rest, are subjected to surgery, radiation, and hormonal therapy for a condition that was never going to harm them. They survive what was never threatening. They credit the system. They tell other men to get tested.

The ERSPC trial, the largest prostate cancer screening trial ever conducted, found that PSA screening reduced prostate cancer mortality by a small absolute amount over thirteen years. To prevent one death, approximately twenty-seven men had to be diagnosed and treated, most of whom would not have died from their disease and many of whom were rendered incontinent, impotent, or both by the intervention.⁸

Every overdiagnosed patient is, by definition, a successful “treatment outcome.” She survived a treatment for a condition that was never going to harm her. The system takes credit. She testifies on its behalf.

Why the System Selects for Evangelism

The four biases would matter less if the visible patients were a representative sample. They are not. The system that produces them also amplifies them.

Hospitals run survivor outreach programs. Pharmaceutical companies fund patient advocacy organizations. The pink ribbon ecology, Susan G. Komen, the National Breast Cancer Foundation, the dozens of subsidiary charities, operates almost entirely on survivor testimony. October fills American mailboxes with pink-ribboned testimonials. The American Cancer Society’s national publicity is built on survivor stories. The patient who survived is the asset.

The corporate machinery built around the survivor is substantial. Estée Lauder co-founded the pink ribbon symbol with Self magazine in 1992 and now sells pink-ribbon cosmetics each October. The National Football League runs an annual “Crucial Catch” campaign with players wearing pink cleats and accessories. Major League Baseball stages pink-bat games on Mother’s Day. Yoplait produced pink-lidded yogurt for two decades under the “Save Lids to Save Lives” campaign. Ford sold pink-ribbon merchandise through “Warriors in Pink.” General Mills, KitchenAid, the National Hockey League, the airlines, the cosmetics counters at every major department store all participate. The advertising spend on these campaigns runs into hundreds of millions of dollars annually, dwarfing the portion of the proceeds that ever reaches research and dwarfing many times over the portion of research funding that addresses environmental causes of breast cancer rather than treatment. The campaigns sell screening. The screening produces patients. Most patients survive, because most of what is found in screening was not going to kill them, and they testify. The testimony funds the next round of campaigns.

The patient who died is, from a marketing perspective, a problem. Her death cannot be celebrated. Her family is often grieving and angry. Her doctors generally do not call the local newspaper. She becomes a statistic in a column nobody reads, while the surviving patient in the next room becomes the face of the cause.

This selection is not a conspiracy. It is a structural feature of how the industry communicates. Living patients can be photographed; dead patients cannot. The living speak at events; the dead are credited, by quiet convention, to “the disease.”

The grateful survivor is also psychologically necessary for the treatment to continue being offered in its current form. The patient who has undergone radical mastectomy, six rounds of chemotherapy, weeks of radiation, and years of endocrine therapy must believe, on pain of intolerable cognitive dissonance, that this was necessary and life-saving. To accept that she may have been treated for a lesion that would not have harmed her, that she lost her breast, her hair, her fertility, her cardiac reserve, perhaps her marriage, to a system that misjudged the threat, is psychologically devastating. The mind protects itself. She becomes an advocate.

The advocate then promotes the system to other women, who undergo screening, get diagnosed, get treated, and become advocates in turn. Each cycle generates more survivors, each of whom credits the system that produced them. The dead and the harmed are silent by definition.

The financial scale of this ecosystem is not small. The United States spends roughly two hundred billion dollars annually on cancer-related medical care. Mammography alone is a multi-billion-dollar industry. The PSA test, despite repeated expert task force recommendations against routine screening, generates billions in downstream procedures. The pink ribbon charities raise hundreds of millions per year, much of which goes to “awareness,” that is, to producing more screening, more diagnoses, more treatment, and more survivors. The asset class, the patient, is manufactured by the process that then takes credit for her survival.

In 2018, a Goldman Sachs equity research report posed the question explicitly to its biotechnology clients: “Is curing patients a sustainable business model?”⁹ The analysts noted that one-time cures undermine recurring revenue streams. The pharmaceutical industry’s most profitable customers are chronic patients, not cured ones. The screening-and-treatment cancer model is, from a financial perspective, an excellent business. It produces patients. It treats them for years. Many of them survive, which is what the model needs them to do, because survivors testify and dead patients do not.

Inside the Testimonial

The cancer survivor has four pieces of information. She was screened. Something was found. She received treatment. She is alive years later. From these facts, she draws a single conclusion: the screening and treatment saved her life.

The inference is intuitive but unsupported. The same four facts admit at least three other explanations.

The screening detected a lesion that would never have harmed her. She survived not because of the treatment but in spite of it. The treatment did damage that she absorbed because the rest of her body was healthy enough to recover.

The lesion was real but slow-growing. She would have lived equally long, with less suffering, by doing nothing.

The lesion was real and biologically active, but her body’s repair mechanisms, what the establishment calls her constitution and what terrain medicine recognizes as her terrain, would have managed it. The treatment was incidental to her survival.

She cannot distinguish between these explanations from her own experience. None of them is available to her introspectively. The only way to determine which is correct, at the level of a population, is the randomized controlled trial, the kind of trial that, in most screening contexts, has either not been done with adequate follow-up or has produced equivocal results that the institutions promoting screening do not publicize.

Her testimonial is sincere. It is also, with respect to the question of whether the treatment worked, evidence of nothing in particular. The dead woman two beds down the hall, who received identical screening and identical treatment and died of cardiotoxic chemotherapy, would have a different testimonial if she could give one. The system that asks the survivor to speak does not ask the dead woman’s family to speak. The asymmetry produces the appearance of a treatment success rate the underlying data does not support.

What Survives the Error

Once you see survivorship bias, you cannot unsee it. What remains is not paranoia but a discipline: asking, in every medical context, which population you are looking at and which population is missing.

When a screening campaign reports that “five-year survival rates have improved,” ask whether overall mortality has changed. Five-year survival can rise to 100% without saving a single life if all the increase comes from earlier detection of lesions that were going to be survived anyway. Overall mortality, deaths per hundred thousand population per year, is much harder to manipulate. It is also the only figure that answers the question the survival rate appears to answer.

A cancer survivor telling you her treatment saved her life can be sincere and still wrong about causation. The conviction is real. The causal claim it carries is not derived from anything she has direct access to. You can be glad she is alive without accepting her account of why.

An oncology center’s published survivor outcomes report a filtered population. Ask about the patients who did not complete treatment. Ask about the patients who died of treatment-related complications and were classified as cancer deaths. Ask about the patients whose follow-up was lost because they moved into hospice care or stopped responding to calls. The shape of the population that gets reported is the shape of the population that survived long enough to be counted.

Facing a screening recommendation yourself, the question to ask is the one the military analysts in 1943 did not ask: what does this examination fail to show me? The bullet holes on the surviving bombers concealed the bullet holes on the destroyed ones. The success stories of the screening industry conceal the women treated for lesions they did not have, the men rendered impotent by surgery for cancers that would never have grown, the second cancers induced by the radiation, and the patients whose treatments killed them and who are now counted, by quiet bureaucratic convention, as having died from their disease.

The full investigative case on these screenings, what they detect, what they miss, what they manufacture, and what they cost, has been documented at length in earlier work.¹⁰ ¹¹ ¹² ¹³ ¹⁴

What the Trials Actually Show

Defenders of mammography routinely cite two trials. The Health Insurance Plan of New York trial, begun in 1963, and the Swedish Two-County Trial, conducted between 1977 and 1985, both reported reductions in breast cancer mortality among screened women. Both have been criticized on methodological grounds. The HIP trial’s randomization was uneven, with baseline differences between arms and exclusion rules applied asymmetrically. The Two-County Trial used cluster randomization that did not consistently balance comparison groups and lacked blinded cause-of-death assessment. Its mortality estimates shifted across successive reanalyses. The Cochrane systematic review of mammography trials classified both as carrying significant risk of bias.⁶

The most rigorously conducted breast cancer screening trial, the Canadian National Breast Screening Study, followed nearly ninety thousand women for twenty-five years. It found no reduction in breast cancer mortality from mammography screening, and no reduction in all-cause mortality.¹⁶

All-cause mortality is the figure that resists the gaming. When a study reports that breast cancer deaths fell among screened women but all-cause deaths did not, the women who avoided a death coded as breast cancer died of something else within the same window: heart failure from chemotherapy-induced cardiotoxicity, second cancers induced by the radiation given for the first, complications from the surgery, strokes after years of endocrine therapy. The Cochrane review and meta-analyses across multiple cancers have repeatedly found that all-cause mortality is essentially identical in screened and unscreened populations. The treatment that prevents one death produces another. The cancer-specific column improves; the death column does not. Survivorship bias gives the illusion of a saved life. All-cause mortality data shows that the life, where treatment did anything at all, was traded rather than added.

The Bombers and the Patients

Abraham Wald died in 1950 in a plane crash in the Nilgiri mountains of southern India. The principle he identified outlived him by three-quarters of a century and now sits, unrecognized by the institutions that depend on it, at the center of the modern medical industry.

The bombers that came back showed where a bomber could be shot and still come back. They did not show where a bomber was vulnerable. The cancer survivors who give interviews, walk in fundraisers, and tell their friends to get screened show where the modern oncology machine is not lethal. They do not show where it works.

The patients who died of their treatments are not at the marathon. The patients treated for lesions that would never have killed them have no way to know they were never in danger. The patients whose cancers were going to be survived regardless have no way to credit their own bodies rather than the chemicals introduced into them. They are the bullet holes on the wings: survivable damage, mapped and celebrated, while the damage that mattered remains invisible because the people who suffered it are no longer in the room.

Wald told the military to armor the engines and the cockpit, the places the surviving planes were not hit. The same instruction applies to medicine: look at what the survivors do not show you. The damage that matters is on the planes that did not come back, and on the patients who can no longer testify.


How to Explain This to a Six-Year-Old

Imagine all your friends drink a magic potion that’s supposed to keep them safe. Half of them disappear. The other half come back and tell you the potion worked great.

If you only listen to the friends who came back, you’ll be sure the potion is wonderful. You’ll tell other kids to drink it too.

But the other half are gone. They can’t tell you whether the potion hurt them. You don’t know whether the potion saved the friends who came back, or whether those friends would have been fine without ever drinking it.

When a cancer survivor tells you the treatment saved her life, listen to her kindly. But remember the friends who disappeared. They are part of the story too.

Quick Reference: The Four Biases

Survivorship bias. Only the living testify. Cancer patients who died of their treatments do not give interviews. The visible patient population is filtered by the treatments themselves.

Lead-time bias. Finding a cancer earlier does not extend life. It extends the time you know about it. Five-year survival rates can rise to 100% without saving a single life.

Length-time bias. Screening preferentially catches slow-growing lesions that were less likely to kill in the first place. Aggressive cancers arise and progress between scans, often undetected until they present symptomatically.

Overdiagnosis. Many screen-detected lesions would never have caused harm. The patient is treated for something that was not a threat, survives easily, and credits the treatment.

References

  1. Mangel, M., & Samaniego, F. J. (1984). Abraham Wald’s work on aircraft survivability. Journal of the American Statistical Association, 79(386), 259–267.
  2. Wald, A. (1943). A Method of Estimating Plane Vulnerability Based on Damage of Survivors. Statistical Research Group, Columbia University. (Declassified and republished by the Center for Naval Analyses, 1980.)
  3. Welch, H. G., Schwartz, L. M., & Woloshin, S. (2000). Are increasing 5-year survival rates evidence of success against cancer? JAMA, 283(22), 2975–2978.
  4. Welch, H. G., & Black, W. C. (2010). Overdiagnosis in cancer. Journal of the National Cancer Institute, 102(9), 605–613.
  5. Bleyer, A., & Welch, H. G. (2012). Effect of three decades of screening mammography on breast-cancer incidence. New England Journal of Medicine, 367(21), 1998–2005.
  6. Gøtzsche, P. C., & Jørgensen, K. J. (2013). Screening for breast cancer with mammography. Cochrane Database of Systematic Reviews, Issue 6, CD001877.
  7. Vaccarella, S., Franceschi, S., Bray, F., Wild, C. P., Plummer, M., & Dal Maso, L. (2016). Worldwide thyroid-cancer epidemic? The increasing impact of overdiagnosis. New England Journal of Medicine, 375(7), 614–617.
  8. Schröder, F. H., et al. (2014). Screening and prostate-cancer mortality in a randomized European study: results of the ERSPC at 13 years of follow-up. The Lancet, 384(9959), 2027–2035.
  9. Richter, S., et al. (2018). The Genome Revolution (biotechnology equity research report). Goldman Sachs Global Investment Research, April 10, 2018.
  10. Unbekoming. The 12 Screenings That Manufacture the Patients They Claim to Find.
  11. Unbekoming. The Screening Trap.
  12. Unbekoming. Breast Cancer: What They Didn’t Tell You.
  13. Unbekoming. The PSA Trap: How a Flawed Test Built a Billion-Dollar Industry and Destroyed Millions of Men.
  14. Unbekoming. The Unbekoming Cancer Compendium.
  15. Sakr, W. A., Grignon, D. J., Crissman, J. D., Heilbrun, L. K., Cassin, B. J., Pontes, J. J., & Haas, G. P. (1994). High grade prostatic intraepithelial neoplasia (HGPIN) and prostatic adenocarcinoma between the ages of 20-69: an autopsy study of 249 cases. In Vivo, 8(3), 439–443.
  16. Miller, A. B., Wall, C., Baines, C. J., Sun, P., To, T., & Narod, S. A. (2014). Twenty five year follow-up for breast cancer incidence and mortality of the Canadian National Breast Screening Study: randomised screening trial. BMJ, 348, g366.

July 5, 2026 Posted by | Science and Pseudo-Science, Timeless or most popular | , | Comments Off on Survivorship Bias: The Logical Error at the Heart of Modern Medicine

“Crimson Thread” apartheid project threatens family already displaced in north Jordan Valley

International Solidarity Movement | July 5, 2026

A family – displaced from Khirbet Samra in July 2025 after years of constant harassment by occupation forces and violent settler Uri Cohen – moved to Atouf, where they purchased a plot of land, determined to defy the occupation’s efforts to destroy their livelihood.

Having to leave their home of more than 20 years was both deeply traumatic and hugely expensive. The 40 dunams in Atouf cost half a million shekels (about 160,000 USD) and transportation costs for all their livestock and belongings were high. Atouf is a primarily agricultural area and there is little grazing land; the family is therefore forced to feed their animals grain and hay. They have also had to spend 150,000 shekels (50,000 USD) on building pens spacious enough to protect their sheep from the heat. The costs of maintaining their flock of 800 sheep have proved unsustainable, and the family has had no choice but to sell 300 of them.

In early December 2025, less than six months after their arrival in Atouf, the family received a demolition order: their property is situated on the path of “Crimson Thread”, a Zionist project that entails the construction of a 22 km long military road with an apartheid fence and a 20m wide “buffer zone” running along eitherside. Stretching from Ein Shibli to Tayasir, the barrier will cut through — and off from one another — the communities of Atouf, Tammoun and Yarza.

On the occupation’s plans, the road cuts almost exactly through the middle of the family property; 36 dunums have already been confiscated, and in January 2026 demolition orders were issued for the remaining 4 dunums, which include the family’s house and the sheep pens.

The family, together with other families and the Tubas municipality appealed the demolition orders, submitting the landowners’ deeds, and the barrier project was temporarily suspended. But then, on June 7, the Israeli court ruled that in 5 of the 7 areas impacted by the project the excavation work could continue (the two sections in which the suspension order still applies are those in the vicinity of Khirbet Yarza). Building demolitions (32 across five sections, 9 of which are residential structures) are still under discussion in court.

Since June 13, the family have had to endure the constant presence of soldiers and bulldozers on their property. The military have installed caravans and tents and dug a trench between the 36 confiscated dunums and the family’s home and pens. Now, the bulldozers are at work preparing for the construction of the barrier; the digging has destroyed the pipes that transport water to the family’s crops and livestock. When a family member went to get water from a well that is situated on the family’s land he was accused by the occupation forces of stealing water.

The family, together with the whole community of Atouf and all the Palestinian villages threatened by “Crimson Thread” are calling for international media and institutional attention in order to expose the brutality of this project which is intended to bisect the Jordan Valley, further isolating Palestinian communities from one another and dramatically worsening their conditions of life.

“during the day they carry out cutting, bulldozing, and destruction works, while at night they fire burning illumination flares over the area. These are dropped near the livestock shelters, creating constant fear, as we worry they might fall onto animal fodder or plastic greenhouses and set everything on fire.” – a family member

July 5, 2026 Posted by | Ethnic Cleansing, Racism, Zionism | , , , , | Comments Off on “Crimson Thread” apartheid project threatens family already displaced in north Jordan Valley

How Germany blew the EU’s chance for information freedom

By Rachel Marsden | RT | July 5, 2026

It’s not every day that an EU member state has the opportunity to push back in favor of freedom. At least not without elections. But a German court did have that chance – and promptly blew it on behalf of European citizens everywhere.

Back in 2022 when the Ukraine war was ramping up, the European Commission made an executive order banning Russian media broadcasting in the EU. Meaning that you couldn’t – and still can’t – access RT from within the EU, either on TV or on the web, without a VPN.

So some folks running a website in Saarbrucken, Germany, near the French border, started including some RT videos in their live feed. They reportedly did this exactly four times, back in 2023. Whoop-dee-do, right?

Wrong. This is the EUSSR we’re talking about, remember?

For this, the accused ended up facing criminal prosecution in Germany for promoting some EU-sanctioned RT Germany content. But it turns out that even the German court in Saarbrucken considering this case had doubts as to whether these guys and their website actually fit the definition of an “operator” under the EU sanction’s language that “prohibits any operator from broadcasting, enabling, facilitating or otherwise contributing to broadcast, any” Russian media content. So the German court referred the question to the European Court of Justice tasked with interpreting and clarifying EU regulations and laws.

Wrong question, guys. Why didn’t you start with asking the ECJ whether the regulation itself, made unilaterally by the EU’s unelected and unaccountable executive branch, is even valid at all under the EU Charter of Fundamental Rights and its Article 11 protecting freedom of expression? The fact that the question wasn’t put to the European court by the German one has spawned a judgment that’s stunning in its failure to interpret the application of any free speech restrictions narrowly enough to avoid the disproportionate limiting of free expression.

The German court missed the forest for the trees and got down into the weeds and all hung up on the comparatively minor issue of whether the website could be considered an “operator” without being a commercial entity. Which the European court then used as a prelude to launch a sweeping McCarthyist “reds under the bed”-style tirade.

“The term ‘disinformation’ is a translation of the Russian word ‘дезинформация’ (dezinformatsiya), coined in the early 1920s by the Soviet intelligence services. Joseph Stalin is credited as being the originator of that term, deliberately making it sound French in order to make it seem Western in origin and thereby enhance its credibility,” wrote the EU court, self-identifying as a history professor. How about if I take that as an open invitation to self-identify as a judge in my capacity as a final-year law student?

The ECJ ultimately ruled that commercialism is irrelevant when the website solicits donations, and had raised over €60,000 within a period of a year. It basically said, look, any commercial nature of the platform risks being a false dichotomy, because who’s to say that the sanctioned entities themselves wouldn’t be paying these independent outlets through donations to promote their banned content: ”Even though, for the purposes of classification as an ‘operator’, no economic activity or income generation is necessary, the context of an appeal for donations enabling such sums to be collected warrants some comment. The fact that some websites are financed by donations rather than by a registered commercial activity justifies increased vigilance as to their possible use as a tool for propaganda purposes, in particular in the case of State-sponsored disinformation campaigns,” the European court ruled. “That lack of clarity makes it more difficult to identify financial flows and, therefore, the actors likely to influence editorial policy or content. It thus creates an environment conducive to interference by external interests, including by third countries, which may intervene directly or indirectly in the production or broadcasting of content.”

Isn’t it the prosecution’s job to present actual evidence and proof of influence through the powerful state-backed legal instruments at its disposal? Shouldn’t the ECJ’s definition of “operator,” if it leans so heavily on the risk of foreign corruption, therefore hinge on whether actual collusion has first been established beyond any reasonable doubt? The ECJ sounds shockingly blasé here about the basic burden of proof for criminal conviction.

This court case had been stayed, or suspended, in Germany pending the ruling by this European Court of Justice. But now it’s free to convict these guys of promoting banned Russian content, under the pretext that just maybe they’re not-so-independent media that schemed on the down-low to distribute Russian media content – something that a lot of people have been doing all over social media of their own volition.

Ultimately, what the buzz around this case effectively does is put a chilling effect on that sharing, and it also risks making people self-censor out of fear of being dragged into court for a judicial proctology exam and having their lives potentially ruined in the press over accusations of Russian collusion. What if these guys (and others) just happen to agree with some of the views expressed on banned Russian media? Who’s going to protect their honestly-held views from establishment authoritarianism?

Hang on, here’s a volunteer for the task.

“Freedom of the press is one of the cornerstones of democracy. And the EU protects what matters, including the right to receive independent, reliable information. The European Media Freedom Act helps keep journalists and sources safe, strengthens editorial independence and protects media organizations from undue interference or legal intimidation. Today, on World Press Freedom Day, we reaffirm our duty to support and protect journalists so they can do their work free from pressure, intimidation, or harm,” says unelected European Commission President and de facto Queen Ursula von der Leyen.

Oh, great. So the same people who censor speech are also its self-appointed defenders. Like an arsonist who goes running around setting fires but also works as a firefighter as their day job.

What’s clear from all this is that EU regulation may look precise on paper, but enforcement isn’t so straightforward. When even member state courts require an official interpretation, then how is the average person supposed to avoid running afoul of the law? The result ends up being less about what’s actually banned and more about what merely feels safe to touch. Not exactly the kind of vibe that one tends to aim for in a democracy.


Rachel Marsden is a columnist, political strategist, and host of independently produced talk-shows in French and English.

July 5, 2026 Posted by | Civil Liberties, Full Spectrum Dominance, Progressive Hypocrite, Russophobia | , , | Comments Off on How Germany blew the EU’s chance for information freedom

‘The Medical-Pharmaceutical Killing Machine: Facing Facts Could Save Your Life’

Children’s Health Defense Team | December 11, 2024

This is a reprint of Chapter 1 in “The Medical-Pharmaceutical Killing Machine: Facing Facts Could Save Your Life,” by Children’s Health Defense.

The book, also available on Amazon documents “systemized medical abuse” that accelerated during the COVID-19 pandemic.

Chapter 1. From Quackery To Criminality

The medicinal use of mercury offers a long-running example of medically induced harm. Although centuries of whistleblowers have warned that dosing patients with it constitutes reckless quackery—and the U.S. government presently places mercury at number three on its “Substance Priority List,” right under arsenic and lead—the heavy metal has figured prominently in the “medical armamentarium” from as far back as the sixth century BC through the present day.

In his important book Evidence of Harm, author David Kirby exposed the pharmaceutical industry’s controversial practice of including mercury preservatives in vaccines. Pointedly using the word “criminal,” Kirby wrote in the foreword to another book about mercury (The Age of Autism by Dan Olmsted and Mark Blaxill) that the “blind belief in a known poison” has been “misguided, immoral, and in some cases, patently criminal.”

The “Messianic” Benjamin Rush

In many ways, the medical practices and beliefs of U.S. Founding Father, physician, and University of Pennsylvania medical school professor Benjamin Rush may have set the stage for modern medicine’s stubborn adherence to dangerous protocols—despite clinical evidence of harm—and its silver-bullet fascination with vaccines “as substitutes for right living,” as Eleanor McBean put it in her 1957 book The Poisoned Needle: Suppressed Facts About Vaccination.

The reportedly “messianic” and “uncompromising” Rush’s late-1700s stock-in-trade was a radical protocol involving bloodletting and purging with—what else?—mercury, a practice that medical historians later dubbed “heroic medicine.” Rush had his own proprietary brand of laxative called “Thunderclappers,” consisting of approximately 60% mercury chloride (also called calomel), which he promoted as “a purgative of explosive power.” As Rush honed his clinical methods, he passed them on to a phalanx of enthusiastic students and disciples during yellow fever epidemics in Philadelphia, where he would bleed and purge up to 100 patients a day. Although use of calomel was not uncommon among doctors of that era, Rush prescribed up to 10 times more than his medical peers and also recommended the removal of huge amounts of patients’ blood, erroneously believing that the blood would replenish itself in a matter of a day or two. “A patient’s failure to respond to this disastrous therapy,” one historian wrote in 2004, “won [the patient] only another round of bleeding and purging.” In another modern writer’s colorful description, “So much blood was spilled in the front yard that the site became malodorous and buzzed with flies.”

No less a figure than George Washington underwent a rapid and gruesome death after Rush protégé Dr. Elisha Dick (and two other Johnny on-the-spot physicians) poisoned Washington with mercury and removed 40% of the beleaguered general’s total blood volume—a quantity that, to this day, “continues to amaze and appall laymen and physicians alike.” From many historians’ point of view, Washington’s doctors caused his death, a death that may well have changed the course of history.

Rush was enthusiastic about promoting his “heroic medicine” protocol, “proclaim[ing] the success of his cure to the public and his medical colleagues” in newspapers, advertisements, and brochures, and even “harangu[ing] people in the streets.” In addition, he was an early and explicit proponent of smallpox vaccination. In 1803, he joined with 30 other Philadelphia doctors in signing a public notice “expressing their confidence in vaccination and recommending it for general use.” Significantly, smallpox vaccination represented a turning point in the “medicalization of the general public” in both early nineteenth-century America and Europe, and a boon for the burgeoning medical profession:

Since the late eighteenth century, doctors had intensified their efforts to win government support for their plans to bring the whole population under medical control. . . . Thus Jenner’s method of cowpox vaccination presented medical practitioners with a new chance to increase their prestige and influence on public health affairs [bold added]. Doctors also foresaw an increase in their income through vaccination fees and hoped to establish themselves, with the help of the vaccine, among those classes of the population who had not consulted doctors before.

From 1813 to 1822, the young U.S. government appointed James Smith as the nation’s “federal vaccine agent,” charging him with “maintaining a supply of the smallpox vaccine and distributing it nationwide”; Smith had been a student of Rush’s at the University of Pennsylvania and was a fellow member of the “well-educated medical elite.” Although other physicians of the day argued that smallpox vaccination was both dangerous and ineffective, then—as now—defenders of the practice prevailed by using “more or less perverted statistics,” with one doctor urging his “professional brethren to be slow to publish fatal cases of small-pox after vaccination” and others passing off vaccine-induced fatalities as some other disease.

Reflecting on Rush’s medical legacy, U.S. Army medical officer P.M. Ashburn made remarks in 1929 that highlight one of the many reasons why Rush’s cautionary tale is still pertinent today. Ashburn wrote that by virtue of Rush’s “social and professional prominence, his position as teacher and his facile pen,” the Philadelphia physician “was more potent in propagation and long perpetuation of medical errors than any man of his day,” thereby “blacken[ing] the record of medicine.” This observation illustrates how social prestige—coupled with “unyielding devotion to dogma”—often helps practitioners of dangerous medicine beat back their critics.

In Rush’s time, those critics included fellow physician Elisha Barlett, who opined about Rush’s medical theories, “In the whole vast compass of medical literature, there cannot be found an equal number of pages containing a greater amount of utter nonsense and unqualified absurdities,” as well as feisty British journalist and pamphleteer William Cobbett, who dared to publish tracts asserting that Rush’s yellow fever treatments were both ineffective and dangerous—and “a perversion of nature’s healing powers.” In response, Rush sued Cobbett for libel and won, in “one of the largest libel awards in American history at the time.”

One of Cobbett’s fascinating observations—which reverberates uncannily in the COVID era—was that extreme fear (in this instance, of yellow fever) made members of the public far more willing to subject themselves to Rush’s “experiments” than they otherwise might have been. Cobbett wrote:

[Rush] seized, with uncommon alacrity and address, the occasion presented by the Yellow Fever, the fearful ravages of which were peculiarly calculated to dispose the minds of the panick-struck people to the tolerance, and even to the admiration, of experiments, which, at any other time, they would have rejected with disdain.

Interestingly, after Rush’s libel victory, Cobbett exacted a modicum of revenge by assembling data from municipal records (acknowledged today as “an epidemiological tour de force”), which pointed to a 56% mortality rate among Rush’s yellow fever patients that contrasted starkly with the physician’s own claim of a greater than 90% survival rate. When word of those dismal statistics got out to the public, Rush’s medical practice suffered. Undaunted, Rush went on to become Treasurer of the U.S. Mint under President John Adams. As the author of America’s first psychiatric textbook, he is also revered today as “the father of American psychiatry.” Rush proposed the same general treatments for madness that he favored for physical ailments, supplemented by straitjackets and other “modes of punishments” for tough cases.

For his part, in 1800, a disgusted Cobbett returned to London, where he continued to hold medicine’s feet to the fire, including condemning smallpox vaccination as “quackery.”

A “Patently Criminal” Model

Some modern medical historians are willing to go so far as to characterize medicine, in periods and places like 18th-century America, as “deplorable,” and to suggest that back then, “a doctor was just as likely to kill you as save you.” Most, however, frame medical barbarity as a thing of the past. Shielded by high-end machines, complex drug technologies, glossy scientific publications, and lingo like “rigorous” and “evidence-based,” the current medical-pharmaceutical-regulatory establishment and its hagiographers would have the public believe that “safe and effective” now rules the day.

There is ample evidence to show that pledges of safety often are either disingenuous or false, and there are indications that Kirby’s description of the medical model as sometimes “patently criminal” was squarely on the mark. At the level of individual medical practitioners, law firms specialized in malpractice note that if a doctor “appears to be indifferent to patients’ well-being or safety,” that indifference can be grounds for criminal liability. A search of the word “criminal” on the website of Medpage Today (a conventional news service that is generally protective of medicine’s reputation) brings up countless articles about doctors and other health care providers running “pill mill” operations, carrying out fraud, taking kickbacks, tampering with drugs, faking data, sexually assaulting or abusing patients, and engaging in other types of “unprofessional” and unethical conduct. The site’s “Investigative Roundups” feature stories (often formulated as questions to soften the impact) with titles like “Columbia protected predator doc?”, “Psychiatrist held patients against their will?”, “$15K surgery shakedown?” or “Doc pushed unneeded surgery?” Other Medpage Today headlines flamboyantly bandy about words like “deadly,” “loophole,” “games,” “tactics,” “unethical,” and “secretive.”

Sometimes, individuals who defend the medical status quo blame whichever reports of misbehavior manage to surface (many do not) on “a few bad apples.” Others, such as Harvard scientist and patient safety advocate Lucian Leape, do the reverse, shifting the blame from “bad people” to nebulous “bad systems;” Leape suggests that a cycle of disrespect is “learned, tolerated, and reinforced in the hierarchical hospital culture.” The fact is, however, that medical harms flow from both individuals and institutions. Most health care providers operate in broader organizational and corporate contexts—and it is policymakers and decision-makers at those levels who often give medical-pharmaceutical corruption and criminality a green light. This is illustrated by the phenomenon (for which there is even an academic field of study) called “clinicide,” defined as serial medical killers responsible for “the unnatural death of multiple patients in the course of treatment;” not infrequently, the killers’ host institutions countenance or “enable” this clinicide by choosing to ignore red flags.

As an extension of the “bad apples” argument, some upholders of the status quo point to the fines that the U.S. Department of Justice (DOJ) routinely levies on hospitals and pharmaceutical corporations, suggesting that these are an adequate mechanism to catch and punish players engaged in malfeasance. However, given that medical-pharmaceutical culprits not infrequently are criminal recidivists and that the fines generally amount to “little more than a slap on the wrist,” it is fair to ask “whether such a monetary punitive system really does much to prevent bad behavior.”

Moreover, DOJ rarely prosecutes or holds corporate leaders accountable, despite having a “powerful legal tool” at its disposal to go after the executives at the helm of medical misconduct; it has done so only 13 times since the year 2000. Instead, many signs point to a wink-and-a-nod sub rosa understanding between the various parties, with the penalties doing nothing to prevent future harms but instead furnishing a generous flow of kickbacks that prosecutors and regulators can funnel into various sectors of the federal budget (see Illegal But Profitable). In fact, under the False Claims Act, the U.S. Department of Health and Human Services (HHS) gets a 20 to 1 return on every dollar it “invest[s] in prosecutions and investigations.”

Illegal but Profitable

In 2018, the nonprofit consumer advocacy organization Public Citizen published a report summarizing 27 years of pharmaceutical industry criminal and civil penalties. The report concluded:

To our knowledge, a parent company has never been excluded from participation in Medicare and Medicaid for illegal activities, which endanger the public health and deplete taxpayer-funded programs. Criminal prosecutions of executives leading companies engaged in these illegal activities have been extremely rare. Much larger penalties and successful prosecutions of company executives that oversee systemic fraud, including jail sentences if appropriate, are necessary to deter future unlawful behavior. Otherwise, these illegal but profitable activities will continue to be part of companies’ business model.

Iatrogenocide Takes Center Stage

Even before COVID, available data indicated that 20th- and 21st-century Western medicine had failed to improve health in any meaningful way, instead trading off the industrial-age diseases of yore for modern chronic disease epidemics, many or most with iatrogenic causes or contributors. Unfortunately, recent events suggest that medicine—forging an unhealthy partnership with government—may now be more dangerous than it has ever been.

Until 2020, the Americans who were most concerned about medical risks and medical criminality belonged to groups already adversely affected, such as those injured by vaccines or opioids. However, with the advent of life-threatening COVID “countermeasures” and lethal protocols in U.S. hospitals and in other countries such as the UK, medical pharmaceutical gangsterism—seemingly occurring with government cognizance—has begun attracting more widespread notice. When governments began parlaying the dubious health “emergency” into an excuse to authorize and mandate the COVID vaccines and boosters—and proceeded full tilt even when unprecedented injuries and deaths immediately began piling up—some segments of the public saw the contours of an officially sanctioned medical crime.

As Holocaust survivor and human rights activist Vera Sharav communicated in her docuseries Never Again Is Now Global, medical coercion and the suspension of constitutional freedoms have never led anywhere good. Unfortunately, history shows that governments intent on “state repression, brutality and genocide” can usually count on the readiness of some doctors to serve as accomplices, even if their complicity has the potential to turn them into “mass murderers on an exponential scale.”

July 5, 2026 Posted by | Book Review, Science and Pseudo-Science, Timeless or most popular | | Comments Off on ‘The Medical-Pharmaceutical Killing Machine: Facing Facts Could Save Your Life’

The Machine

An Essay on the American Vaccine Program from License to Prosecution

Lies are Unbekoming | July 3, 2026

On November 14, 1986, Ronald Reagan signed the National Childhood Vaccine Injury Act into law.¹ The legislation ended more than a decade of tort litigation against vaccine manufacturers by transferring civil liability for injury and death from the companies producing the products to the American taxpayer. The pharmaceutical industry had threatened to leave the childhood vaccine market. Reagan’s signature ensured they would stay, at a price paid by parents who would never be told what had been arranged on their behalf.

Twenty-five years later, in Bruesewitz v. Wyeth, the Supreme Court closed the last remaining exit. The 2011 decision, written by Justice Antonin Scalia, held that federal law preempts all design-defect claims against vaccine manufacturers in state courts.² Justice Sotomayor’s dissent, joined by Justice Ginsburg, identified the practical effect: no federal agency, no state court, no jury of citizens would henceforth ensure that vaccine manufacturers accounted for scientific advances when designing their products. The manufacturers had been placed outside the accountability structure that governs every other industry in the United States.

The 1986 Act and the 2011 ruling together defined the shape of what now exists. Every function of the vaccine program — licensing, recommendation, purchase, safety monitoring, patent holding, research funding, injury adjudication, and courtroom defense — resides in the federal government. When the products kill a child, the state prosecutes the parents.

Leslie Manookian, founder of the Health Freedom Defense Fund, mapped this architecture in a twelve-point summary published to her readers.³ What follows walks through the machine she described, in five stages. Each stage encloses the next. By the fifth, the shape of the trap around the American parent becomes fully visible.

1. The License

The Food and Drug Administration licenses vaccines on the basis of clinical trials that do not use inert placebo controls. This fact is documented in the FDA’s own package inserts and in sworn testimony by the industry’s most senior figures.

In January 2018, attorney Aaron Siri deposed Dr. Stanley Plotkin in New Hope, Pennsylvania — the vaccinologist widely regarded as the industry’s founding figure and co-editor of the standard reference textbook Plotkin’s Vaccines.⁴ Under oath, Siri walked Plotkin through the pre-licensure clinical trials for each product on the recommended childhood schedule. The pattern that emerged was uniform.

The safety review period following each dose was 48 hours for the IPOL polio vaccine. 48 hours for ActHIB. Four days for Engerix-B, the hepatitis B vaccine administered to newborns on their first day of life. Five days for Recombivax HB, the other hepatitis B product. Siri produced, for comparison, the package insert for Enbrel — a drug given to adults with rheumatoid arthritis — and asked Plotkin to confirm that its pre-licensure clinical trials monitored patients for up to 80 months. Plotkin confirmed. A drug given to sick adults was studied for six and a half years. Vaccines given to healthy newborns were studied for 48 hours to five days.

Plotkin then confirmed, product by product, that these trials had no saline placebo control group. Not Recombivax HB. Not Engerix-B. Not IPOL, whose trial subjects received the polio vaccine concurrently with DTP, making it impossible to attribute any reaction to either product. Not ActHIB. The MMR II vaccine, which Plotkin himself was present for the licensure of, had, in his own words, no control group “for the studies that I’m recalling.” When the Hiberix Hib vaccine was later licensed, the manufacturer used ActHIB itself as the “placebo” — testing one Hib vaccine against another.

On the necessity of a saline control, Plotkin was direct: “Without a control group, if you’re looking for a phenomenon occurring in the vaccine group, you cannot judge that phenomenon without having a control group.” That is the industry’s founding figure, testifying under oath, describing the epistemic condition of the products his industry markets.

The pattern in the trials produces a specific consequence. When a new vaccine is tested against an existing licensed vaccine as its control, any injury rate common to both groups becomes invisible. The comparison measures relative difference, not absolute harm. If the existing vaccine produces seizures at a rate of 1 in 500, and the new vaccine produces seizures at a rate of 1 in 500, the trial reports no significant difference — and both products remain on the market.

The Gardasil trial illustrates what happens when a saline group is included but the result is inconvenient. Merck’s pre-licensure clinical trial for its HPV vaccine assigned 9,412 subjects to a “placebo” arm. Of these, only 594 received actual saline. The remaining approximately 8,800 received AAHS — the aluminum-containing adjuvant used in the Gardasil formulation itself. Merck reported the two groups combined, showing 2.3% of the “placebo” arm developing what the trial recorded as systemic autoimmune events, matched by 2.3% in the Gardasil arm. The vaccine was declared safe on the strength of no difference.

Siri produced the underlying trial data. Broken out separately, the saline placebo group of 594 girls and women showed zero such events. The aluminum group showed approximately 2.5%. Merck had recorded the difference and reported the combination.

Plotkin was asked why the two groups had been combined for that analysis when they were broken out separately for local reaction analysis on the preceding pages. His response, verbatim: “So going into the study, they just assumed aluminum wouldn’t cause autoimmunity and so that’s how they proceed in designing it.” A pre-licensure trial for a product administered to schoolgirls declared the vaccine safe by defining the aluminum adjuvant as inert, then combining subjects receiving that adjuvant with subjects receiving nothing.

Once a vaccine reaches the schedule, the failure to test it against saline becomes permanent. For each product Siri walked Plotkin through, he asked whether a proper placebo-controlled study could now be conducted. Plotkin confirmed, product by product, that it could not — running such a trial would be “unethical” in children whose vaccines are already recommended. The absence of a control group at the point of licensure becomes the reason no control group can ever be introduced. The regulatory record is locked at the point of the initial deception.

When a Freedom of Information Act request submitted by the Informed Consent Action Network in 2018 asked the Department of Health and Human Services to produce the biennial vaccine safety reports required by Section 300aa-27 of the 1986 Act, HHS was forced to respond that it had not produced a single such report in the thirty-two years since Reagan signed the law.⁵ The statutory obligation to review safety had been ignored for the entire life of the program.

The FDA license then triggers the second function. The Centers for Disease Control and Prevention convenes the Advisory Committee on Immunization Practices, which votes on whether to add the newly licensed vaccine to the recommended childhood schedule. ACIP members are drawn from the same institutional networks that developed and defended the products. Once added, the vaccine appears on the schedule that is distributed to every state health department in the country. The recommendation is not a mandate. It becomes one at the next stage.

Under oath in the same deposition, Plotkin acknowledged that he had served as medical and scientific director of Sanofi Pasteur in the 1990s, that he operated a personal consulting entity called Vaxconsult, and that he had received payments over the preceding two decades from Merck, GSK, Pfizer, Sanofi, and, in his own phrasing, “essentially all of the major manufacturers.” He had also consulted for the FDA. The industry’s founding figure had confirmed the case against the products his industry markets. He was also paid by every major manufacturer of those products.

Plotkin Under Oath: Nine Hours That Exposed the Vaccine Industry

2. The Mandate

The federal government does not directly mandate childhood vaccines. That function is delegated to the states.

Every state in the union has passed legislation requiring specified vaccines for school attendance. The specific list varies. The mechanism is uniform. Parents who wish to enroll their children in public school — and in many states private school — must produce documentation that their children have received the vaccines on the state’s list. The state list is drawn from the CDC schedule; the CDC schedule from the ACIP recommendation; the ACIP recommendation from the FDA license. The FDA license rests on trials that were never controlled against a genuine placebo.

The chain is complete before the parent enters the pediatrician’s office.

Under the Vaccines for Children program, established in 1993, the federal government purchases half of all childhood vaccines administered in the United States. Recent VFC spending has exceeded $5 billion annually.⁶ The federal government is the largest single purchaser of the products it licenses, the products it recommends, and the products the states mandate.

This creates a market structure without parallel elsewhere in American pharmaceutical policy. The maker of a blood pressure medication faces market discipline. Doctors may prescribe it or not, patients may fill the prescription or not, insurance may cover it or not. The maker of a childhood vaccine faces no equivalent constraint. The state compels administration; the federal government guarantees a buyer; demand is legislated. Revenue is secured before a single dose is delivered.

The mandate has hardened as it has aged. Every state at some point permitted medical, religious, and in some cases philosophical exemptions from the vaccine schedule. Over the past decade, state legislatures have moved to close them. California eliminated its personal belief exemption in 2015 through SB 277 following the Disneyland measles cluster. In 2019, New York eliminated its religious exemption; Maine followed the same year. Connecticut eliminated its religious exemption in 2021. The pattern has been consistent: a highly publicised incident, a legislative response drafted with industry input, and the removal of the exit ramp. The federal government does not need to mandate. The state legislatures have been prevailed upon to do it, and to progressively narrow the terms under which the mandate can be refused.

Leslie Manookian, in the interview she gave me,¹⁹ described the shape of what has been built here. “When we succeed and thrive outside the extant medical paradigm, we pose an existential threat to the medical complex which is why the main actors fight our information, experiences, and independence so fervently.” The compelled purchase is what makes the mandate machinery operate. Without it, the products would compete on their merits. With it, they do not compete at all.

Interview with Leslie Manookian

3. The Shield

The 1986 Act shielded manufacturers from every category of liability that governs other industries. The immunity covered injuries caused by design choices themselves — the composition of the product, the adjuvants used, the decisions about testing. A safer alternative product could exist and the manufacturer could refuse to adopt it, and the injured child’s family could not sue.

Justice Scalia’s opinion in Bruesewitz addressed a case brought by Robalee Bruesewitz on behalf of her daughter Hannah, who had suffered residual seizure disorder and developmental delay after receiving the DPT vaccine manufactured by Wyeth. The Bruesewitz family had exhausted the Vaccine Injury Compensation Program. They then attempted to sue Wyeth in state court, arguing that a safer alternative vaccine design existed and Wyeth had refused to adopt it. The Supreme Court held that federal law preempts such claims. The manufacturer’s choice to continue producing a design that injured children could not be litigated.

Sotomayor’s dissent identified the consequence. Vaccine manufacturers now occupy a regulatory space in which no external mechanism — regulatory agency, court, or jury — holds them accountable for design decisions. This is not an inference. It is a description of the legal structure the majority created.

Behind the shield sits a further conflict. The Department of Health and Human Services — the parent agency of the FDA, the CDC, the National Institutes of Health, and the Health Resources and Services Administration that runs the injury compensation program — holds patents on multiple childhood vaccines. HHS scientists Douglas Lowy and John Schiller developed the recombinant protein technology underlying Merck’s Gardasil and receive royalties on its sale.⁷ Similar patent and royalty arrangements extend to other products in the childhood schedule. The regulator collects revenue on the products it approves.

The research infrastructure that would produce independent safety findings is subject to a parallel capture. Studies funded by the CDC, the NIH, or by the manufacturers themselves consistently produce findings favorable to the schedule. The vaccinated-versus-unvaccinated comparison studies that would settle the fundamental question about long-term outcomes have not been funded. When independent researchers attempt them — Anthony Mawson’s 2017 study of homeschooled populations,⁸ Paul Thomas’s cohort analysis of his own pediatric practice⁹ — the results are attacked, retracted, or ignored, and the researchers face professional consequences.

The capture extends inside the agencies themselves. In August 2014, Dr. William Thompson, a senior epidemiologist at the CDC and co-author of the 2004 DeStefano study widely cited to reject any link between the MMR product and neurodevelopmental injury, submitted a statement through his attorney acknowledging that he and his co-authors had “omitted statistically significant information” from the published paper and had disposed of documents to conceal the omission.¹⁰ The withheld data showed an elevated risk of neurodevelopmental injury among African American boys who received the injection before thirty-six months of age. Thompson’s disclosure was made under whistleblower protection. Congress has never subpoenaed him to testify. The DeStefano paper remains uncorrected.

Merck faced a parallel qui tam action from two of its own virologists, Stephen Krahling and Joan Wlochowski, who alleged in a federal filing that Merck had falsified mumps vaccine efficacy data submitted to the FDA over the course of a decade.¹¹ The case, filed in 2010, moved slowly through the courts. The Department of Justice declined to intervene. Merck retained its exclusive contract to supply mumps vaccine to the U.S. government. The plaintiffs’ allegations of test manipulation entered the public record and produced no regulatory action.

The shield is a network. Liability preemption from Congress protects the manufacturer. Patent revenue aligns the regulator with the products it approves. Captured research funding directs the studies that might identify harm away from the questions that would find it. Judicial preemption then blocks any citizen who attempts to litigate the design decisions the products embody. Each layer supports the others. The whole structure is invisible to the parent standing in a pediatrician’s office being told the shot is safe.

No Liability, No Studies, No Accountability: The Vaccine System Aaron Siri Exposed in Federal Court

4. The Monitor Becomes the Promoter

The Centers for Disease Control and Prevention operates the Vaccine Adverse Event Reporting System. It also runs the promotional campaigns that place vaccination on the pediatric schedule. The agency responsible for detecting harm from the products is the same agency responsible for driving their uptake.

The conflict is not theoretical. Harvard Pilgrim Health Care, under a grant from the Agency for Healthcare Research and Quality within HHS, conducted an internal study of VAERS reporting rates in a Massachusetts patient population between 2007 and 2010. The study found that fewer than 1% of vaccine adverse events were being captured by the reporting system.¹² When the researchers attempted to communicate their findings to the CDC in order to develop improved reporting mechanisms, the agency stopped responding to their emails. The grant ended. The improved reporting system was never built.

The passive reporting infrastructure that captures under 1% of injuries then becomes the basis for the CDC’s public assurances that adverse events are rare.

The injury table itself has been subject to steady contraction. When the Vaccine Injury Compensation Program began in 1988, the injury table included a broader range of conditions presumed to be caused by vaccination, with corresponding timelines within which onset would qualify a case for compensation.¹³ Over the following decades, categories were removed or narrowed. Sudden Infant Death Syndrome, initially compensable when it followed vaccination within a specified window, was removed. Neurodevelopmental injury, briefly acknowledged as a category during the 1990s when concerns about the MMR product and other injections emerged, was removed. The seizure timelines were narrowed. Encephalopathy definitions were tightened.

The 1995 amendment illustrates the pattern. Residual seizure disorder — a category under which many families of children who had suffered seizures after DPT vaccination had successfully claimed compensation — was removed. Encephalopathy criteria were revised in ways that made the diagnosis nearly impossible to satisfy. The Advisory Commission on Childhood Vaccines, which recommended the changes, drew a majority of its membership from the same medical-institutional networks that administered and defended the vaccine schedule. Petitioners whose cases had been filed under the earlier table found themselves adjudicated under the new one. Cases that would have succeeded were denied.

Each removal reduced the number of compensable claims. The fund benefited. So did the manufacturers whose products would otherwise be more clearly implicated in the injury pattern.

The Institute of Medicine, tasked periodically with reviewing whether specific vaccines cause specific injuries, has repeatedly concluded that the evidence is insufficient to accept or reject a causal relationship for a majority of the injury-outcome pairs it examines.¹⁴ This finding — insufficient evidence — is then used in the injury compensation courtroom to deny claims. The absence of evidence functions as evidence of absence, produced by the very research infrastructure that would have to fund the studies to end the insufficiency.

The industry’s founding figure confirmed the position under oath in the same deposition. Asked directly whether he could make the scientific statement that childhood vaccines do not cause autism, Plotkin answered: “As a scientist, I would say that I do not have evidence one way or the other.” The IOM had found no study establishing that the DTaP or Tdap products do not cause autism. Plotkin acknowledged that no such study existed and that he personally held no evidence to support the claim his industry has spent three decades making.

The parent whose child seized within twelve hours of vaccination, developed encephalopathy, and never recovered enters a system that was prepared for her arrival. The injury table’s timeline for seizure onset has been shortened past the point where her child’s case qualifies. The IOM has declared the evidence insufficient. VAERS captured her report and did nothing with it. The monitor was never separate from the promoter.

5. The Court and the Blame

The Vaccine Injury Compensation Program is administered by the U.S. Court of Federal Claims. It is not a court in the ordinary sense. The proceedings involve no juries, no meaningful discovery, and no Article III judges — no judges appointed for life under the constitutional protections designed to insulate the judiciary from executive influence.

Cases are heard by “Special Masters,” Article I officers appointed by the Chief Judge of the Court of Federal Claims to seven-year terms. The Special Masters are drawn from a pool of attorneys with prior government experience. The Department of Justice provides the attorneys who defend against injury claims. HRSA administers the fund. The petitioner’s attorneys are paid from the same fund out of which awards are made.

Every party in the courtroom — the judge, the government’s defense attorneys, the fund itself, and the petitioner’s legal counsel — is paid by the federal government. The injured child’s family stands before a tribunal in which no independent party has an interest in a finding of injury.

The statistics reflect the structure. The majority of petitions filed with the VICP have been dismissed rather than compensated over the life of the program.¹⁵ Of the cases that succeed, the majority are settled rather than adjudicated on the merits, with no admission that the vaccine caused the injury. The compensation cap for a vaccine-caused death — $250,000 — has not been raised since the statute was passed in 1986.

The excise tax that funds the program is $0.75 per antigen per dose. The fund now holds over $4 billion.¹⁶ The families whose children were injured cannot access it through the ordinary legal system because the ordinary legal system has been closed to them.

This is the structure Leslie Manookian described in her twelve-point summary. Her exact phrasing on the final function is worth returning to: “So, parents who’ve already suffered an unimaginable tragedy are up against a govt court staffed by govt paid special masters and attorneys with no due process defending a govt licensed and govt mandated product for which they blame the victims for harm.”

The final phrase — “they blame the victims for harm” — describes the twelfth function of the machine. When a child collapses after vaccination with the sudden onset of retinal hemorrhages, subdural hematoma, and cerebral edema — the triad — the diagnosis assigned in emergency departments and coroner’s offices is “shaken baby syndrome” or its rebranded successor, “abusive head trauma.” The triad is presumed diagnostic of parental abuse. The parents are arrested.

The vaccine reaction that produces the identical triad — through encephalopathy, elevated intracranial pressure, and hemorrhagic events following injection — is not considered in the differential diagnosis.¹⁷ The diagnostic criteria for “shaken baby syndrome” were developed without accounting for it. The emergency physician, the coroner, and the child protective services investigator have all been trained within an institutional framework in which vaccine injury of this magnitude does not exist.

Alan Yurko’s ten-week-old son died in November 1997 shortly after receiving a round of childhood vaccinations. Yurko was convicted of first-degree murder in 1999 on the basis of the triad diagnosis and sentenced to life plus ten years in Florida state prison. He was released in 2004 after independent medical review of the case demonstrated that the shaking diagnosis could not be sustained and post-conviction proceedings established alternative medical explanations for the child’s injuries.¹⁸ Yurko is one documented case. There are others. The precise number is unknown because the diagnostic framework prevents the question from being asked.

A parent whose child dies after vaccination faces a compound structure. The vaccine that caused the death is licensed by the federal government, recommended by the federal government, purchased by the federal government, and defended in the injury court by the federal government. The manufacturer is shielded from civil liability by federal statute and Supreme Court precedent. The injury table does not recognize the death as vaccine-caused. The state, meanwhile, has assigned the triad diagnosis and turned the case over to the district attorney. The parent must now prove — in a criminal court, against the state — that the child was not shaken.

The Vaccine Court (2014)

The Position

Robalee Bruesewitz spent nearly two decades in litigation on behalf of her daughter. The Supreme Court’s ruling denied her family relief and closed the door behind them for every family that would come after. The 1986 Act had shifted liability from the manufacturer to the taxpayer. Bruesewitz confirmed that the shift was permanent and that no design decision made by the manufacturer could be challenged in any court open to ordinary Americans.

This is the position in which the American parent now stands. Her child’s pediatric visit will produce a recommendation to administer products licensed on the basis of trials that were never controlled against saline. The state will require their administration for school attendance. When injury results, over 99% of adverse events never reach VAERS at all, and the reports that do reach it change nothing. A family that attempts compensation will petition a court in which every party is paid by the federal government to defend the products or administer the fund. And when death occurs with the triad present, the emergency department’s diagnostic framework will not include vaccine reaction in the differential, and the parent enters the criminal jurisdiction as the presumed cause of the child’s death.

There is no exemption from this structure that carries no cost. State legislatures have progressively narrowed medical and religious exemptions; declining vaccines removes a child from school; injury bars a family from ordinary civil courts. And when death is accompanied by the triad, the state prosecutes the parent for the death.

Leslie Manookian described this arrangement, at the close of her twelve-point post, as “crony capitalism at best and pure evil fascism at worst.” The characterization is precise. A private industry produces the product. The state compels its administration, indemnifies the manufacturer against claims of harm, and prosecutes the parent when the harm arrives.

The machine’s design serves the flow of money and the concentration of power. Every safeguard the ordinary citizen might rely on — informed consent, product liability, judicial review, jury trial, prosecutorial restraint — has been removed at the point where the childhood vaccine schedule intersects with the American family. The parent who accepts the recommendation and whose child is injured has no meaningful path to redress. Refusal costs school access. Death with the triad opens the parent to criminal prosecution for a killing they did not commit.

This is the environment in which every American child is now born. The machine was assembled piece by piece across four decades, ratified by every institution that could have prevented it, and defended by the same institutions today. What Leslie Manookian named as crony capitalism at best and fascism at worst describes a working system, operating as designed, in a country that once organised its politics around the presumption that no such system could be permitted to form.

For a Six-Year-Old

There is a big company that makes shots.

The government helps the company make the shots and sell them. The government tells your school that you have to get the shots before you can come to school.

Nobody checks the shots very well. The people who are supposed to check work with the company. So the shots go out into the world before anyone really knows if they are safe.

When a child is hurt by a shot, the family cannot go to a normal judge. There is a special room where a different kind of judge decides. That judge is paid by the government. The lawyers on the other side are paid by the government. The government made the shot rules. The government bought the shots. And the government decides whether the shot hurt you.

Most families are told the shot did not hurt their child, even when it did.

When a shot makes a baby die, the doctors sometimes think the mother or father shook the baby. The parents can be arrested. They can go to prison. For what the shot did.

The company that made the shot never gets in trouble. The company keeps making the shots. Your school keeps requiring them. The next family goes through the same door.

That is the machine.


References

¹ National Childhood Vaccine Injury Act of 1986, Public Law 99-660, 42 U.S.C. § 300aa-1 et seq.

² Bruesewitz v. Wyeth LLC, 562 U.S. 223 (2011).

³ Leslie Manookian, twelve-point summary post, X (@LeslieManookian), July 3, 2026, status/2072712451800625369.

⁴ Deposition of Stanley A. Plotkin, M.D., taken January 11, 2018, in Matheson v. Schmitt, State of Michigan, Circuit Court for the County of Oakland, Family Division, Case No. 2015-831539-DM; transcript published via Informed Consent Action Network.

⁵ ICAN v. HHS, correspondence dated July 9, 2018, in response to FOIA request; HHS acknowledged no biennial reports produced under 42 U.S.C. § 300aa-27(c).

⁶ Vaccines for Children Program expenditure data, Centers for Disease Control and Prevention; annual VFC purchasing figures.

⁷ U.S. Patents 5,437,951 and related — Lowy, Schiller et al., “Self-Assembling Recombinant Papillomavirus Capsid Proteins,” assigned to the United States Department of Health and Human Services; licensed to Merck & Co. for Gardasil.

⁸ Mawson AR et al., “Pilot comparative study on the health of vaccinated and unvaccinated 6- to 12-year-old U.S. children,” Journal of Translational Science, 2017.

⁹ Thomas JL, Lyons-Weiler J, “Relative Incidence of Office Visits and Cumulative Rates of Billed Diagnoses Along the Axis of Vaccination,” International Journal of Environmental Research and Public Health, 2020.

¹⁰ Statement of William W. Thompson, Ph.D., through counsel Rick Morgan, August 27, 2014; documentation regarding DeStefano DA et al., “Age at first measles-mumps-rubella vaccination in children with autism and school-matched control subjects: a population-based study in metropolitan Atlanta,” Pediatrics, 2004.

¹¹ United States ex rel. Krahling and Wlochowski v. Merck & Co., Inc., No. 2:10-cv-04374, U.S. District Court for the Eastern District of Pennsylvania, complaint filed 2010.

¹² Lazarus R et al., “Electronic Support for Public Health–Vaccine Adverse Event Reporting System (ESP:VAERS),” Grant Final Report, Harvard Pilgrim Health Care, Inc., 2011 (AHRQ Grant ID R18 HS 017045).

¹³ Vaccine Injury Table history, Health Resources and Services Administration; successive amendments to 42 C.F.R. § 100.3.

¹⁴ Institute of Medicine (now the National Academy of Medicine), Adverse Effects of Vaccines: Evidence and Causality (2011) and predecessor reports.

¹⁵ Health Resources and Services Administration, VICP claim adjudication statistics.

¹⁶ Vaccine Injury Compensation Trust Fund monthly balance report, U.S. Department of the Treasury.

¹⁷ Michael Innis, “Vaccines, Apparent Life-Threatening Events, Barlow’s Disease, and Questions about ‘Shaken Baby Syndrome,’” Journal of American Physicians and Surgeons, 2006; Harold Buttram and Alan R. Yurko, “Shaken Baby Syndrome or Vaccine-Induced Encephalitis?” Medical Sentinel, subsequent case documentation.

¹⁸ State of Florida v. Alan R. Yurko, Ninth Judicial Circuit, 1999; post-conviction proceedings and release 2004; contemporaneous medical review including Harold E. Buttram, M.D.

¹⁹ Unbekoming, “Interview with Leslie Manookian, Health Freedom Defense Fund,” Lies are Unbekoming, Substack, April 13, 2024.

July 4, 2026 Posted by | Corruption, Deception, Progressive Hypocrite, Science and Pseudo-Science, Timeless or most popular | Comments Off on The Machine

West African states begin withdrawal from ICC

MEMO | July 3, 2026

Burkina Faso, Mali and Niger have officially begun a one-year process to withdraw from the International Criminal Court (ICC), the court has announced.

The three West African countries previously said they would leave the ICC, describing it as “a tool of new colonial oppression,” according to Reuters.

The presidency of the ICC’s governing body confirmed that Burkina Faso, Mali and Niger had submitted formal notices of withdrawal, triggering a one-year process to leave the Rome Statute, the treaty that established the court.

In a statement, the presidency said the move could weaken global efforts to end impunity and undermine the pursuit of justice. It urged the three countries to remain committed to the Rome Statute.

The statement also stressed that withdrawal does not release a state from any obligations arising during its membership of the Rome Statute.

July 4, 2026 Posted by | Progressive Hypocrite | , , , , | Comments Off on West African states begin withdrawal from ICC

Extremists attack five Malian towns in coordinated dawn attack

Al Mayadeen | July 4, 2026

Mali’s army announced on Saturday that insurgents launched attacks before dawn against its positions in Aguelhok, Anefis, Gao, Sévaré, and Kenieroba, spanning the country’s north and center. Fighting in the different locations began around 5 am local time.

The army says the assaults were attempted strikes on its positions, according to a statement carried on state television.

In Gao, a local official told Reuters that gunfire and rocket fire had targeted a military camp since before dawn. Explosions were also reported in Sévaré, with aircraft later spotted flying over the area, a security source told AFP.

In Kenieroba, roughly 74 kilometers from Bamako, a major prison complex holding extremist prisoners came under attack. There were no immediate reports of casualties.

FLA claims gains in Anefis

The Azawad Liberation Front (FLA), a Tuareg-led separatist movement, confirmed it carried out the assault on Anefis, in the northeastern Kidal region.

For his part, spokesperson Mohamed Elmaouloud Ramadane told Reuters that several army positions in the town had fallen and that clashes were ongoing inside it.

A resident reached by AFP said armed fighters had entered the town but that the army camp had not yet fallen, and government forces were still resisting.

JNIM, the al-Qaeda-linked coalition that has also operated alongside the FLA, had not issued a claim as of Saturday.

Anefis and Aguelhok are the only locations in the Kidal region where Malian troops have maintained a presence since the collapse of government control there in late April, when FLA and JNIM fighters seized the city of Kidal itself.

Russian forces, deployed to Anefis after that offensive, are also stationed in the area, making it a focal point for both Bamako and Moscow’s regional military presence.

Part of a broader pattern since April

Saturday’s attacks come just over two months after JNIM and the FLA carried out a coordinated wave of strikes on military and administrative targets across Mali, including in Bamako, Kati, Gao, Sévaré, and Kidal.

That offensive killed Defense Minister Sadio Camara, whose responsibilities were temporarily transferred to President Assimi Goïta, and led to the withdrawal of Malian and Russian forces from Kidal and other northern towns.

Russia’s Defense Ministry described the April events as a foiled coup attempt involving roughly 12,000 fighters, it said were trained with Western support.

July 4, 2026 Posted by | Militarism | , | Comments Off on Extremists attack five Malian towns in coordinated dawn attack

Explainer: Which foreign delegations attended the funeral of martyred Leader of the Islamic Revolution?

Press TV – July 4, 2026

The funeral ceremony for the martyred Leader of the Islamic Revolution, Ayatollah Seyyed Ali Khamenei, brought together one of the largest gatherings of foreign dignitaries in Iran in recent decades, with representatives from across Asia, Africa, Europe, the Americas, and major international organizations attending the event in Tehran.

The delegations included presidents, prime ministers, parliamentary speakers, foreign ministers, senior government officials, political leaders, and representatives of religious organizations and resistance movements, underscoring the broad international participation in the ceremony.

Asia

Asia accounted for the largest share of official delegations.

From West Asia, Iraq sent one of the largest delegations, including Kurdistan Region President Nechirvan Barzani, Parliament Speaker Mahmoud al-Mashhadani, senior officials, and representatives of the Popular Mobilization Forces (PMF).

Saudi Arabia was represented by Deputy Foreign Minister Waleed Al-Khuraiji, while Oman sent the chairman of its State Council and Qatar was represented by Parliament Speaker Hassan bin Abdullah Al Ghanim.

Shia community representatives also attended from Bahrain and several other Persian Gulf countries.

Lebanon dispatched Defense Minister Michel Menassa alongside senior delegations from Hezbollah and the Amal Movement.

Yemen was represented by Vice President Mahmoud al-Junaid and an Ansarullah delegation.

Palestinian groups also attended, including senior Hamas leaders and Islamic Jihad Secretary-General Ziyad al-Nakhalah.

From the wider Asian region, Pakistan sent one of the highest-level foreign delegations, headed by Prime Minister Shehbaz Sharif and Army Chief Field Marshal Syed Asim Munir. The delegation also included the Senate speaker, senior government officials, and religious leaders.

Afghanistan was represented by delegations from the Taliban administration and the Afghan resistance.

India sent a special government envoy at the deputy foreign minister level.

China was represented by He Wei, Vice Chairman of the Standing Committee of the National People’s Congress.

Tajik President Emomali Rahmon attended the ceremony in person, while Armenia was represented by Prime Minister Nikol Pashinyan. Georgia sent President Mikheil Kavelashvili along with a Muslim delegation.

Türkiye dispatched Vice President Cevdet Yılmaz, together with political and party representatives.

Turkmenistan was represented by Gurbanguly Berdimuhamedow, Chairman of the People’s Council and National Leader.

Among other participants were Azerbaijan’s parliament speaker, Kazakhstan’s foreign minister; the parliamentary speakers of Kyrgyzstan, Uzbekistan, Bangladesh, and Sri Lanka; Thailand’s deputy prime minister; Malaysia’s agriculture minister; Myanmar’s special envoy; and official delegations from South Korea and North Korea.

Africa

Several African governments were represented by ministerial- or cabinet-level delegations.

Egypt sent its Senate speaker.

South Africa, Burkina Faso, the Democratic Republic of the Congo, Namibia, Tanzania, and Tunisia all sent official representatives.

Nigeria and Senegal also dispatched delegations to participate in the funeral ceremonies.

Europe and the Americas

Russia sent Dmitry Medvedev, Deputy Chairman of the Russian Security Council, as President Vladimir Putin’s special representative.

Belarus was represented by its parliament speaker, while Serbia sent its communications minister. Bulgaria also dispatched parliamentary and political representatives.

Germany was represented by members of the country’s Shia community.

From Latin America, Cuba sent its higher education minister as a special representative, while Nicaragua was represented by Foreign Minister Valdrack Jaentschke.

International organizations

The ceremony also drew senior representatives of several international organizations.

The Shanghai Cooperation Organization (SCO) was represented by Secretary-General Nurlan Yermekbayev, while the Organization of Islamic Cooperation (OIC) sent Deputy Secretary-General Tariq Ali Bakheet.

The D-8 Organization for Economic Cooperation and the Economic Cooperation Organization (ECO) were represented by their respective secretaries-general.

July 4, 2026 Posted by | Solidarity and Activism | , , , , , , , , , , , , , , , , , , | Comments Off on Explainer: Which foreign delegations attended the funeral of martyred Leader of the Islamic Revolution?

UK and Israel criticized for persecuting anti-genocide advocates

Protesters rally in London in support of Dr. Ghassan Abu-Sittah
Press TV – July 4, 2026

Protesters gathered outside the General Medical Council’s headquarters in London to slam the council’s attempt to silence those speaking out about the Israeli genocide in Gaza.

Video Report

Protesters describe the surgeon as one of the world’s leading war doctors and argue that the regulator’s actions amount to an attempt to silence those who speak publicly about the realities of war,

So we are demonstrating in front of the GMC, because the GMC has decided to appeal against the rulings of two of its own tribunals, so that the High Court would allow it to try me for a third time, in order to get the right political result that it wants.

The GMC is conducting a political campaign against, not just myself, but every doctor who’s spoken up against the genocide, in order to silence us, in the service of the genocidal project. – Dr Ghassan Abu Sittah, British-Palestinian Surgeon

Doctors, campaigners, and members of the public traveled to attend the demonstration, asserting that the proceedings are about more than one individual, warning that they could have a chilling effect on healthcare professionals speaking about humanitarian crises.

Actually, there probably were a group of lawyers set up by the Israelis again to pursue highly charged politicized campaigns against professionals and workers in this country who stand against genocide.

So, really, it’s the action of how the British government and the Israelis who are trying to persecute and outlaw speech in support of Palestine in the heartland of Britain.

Actually, from, we know where our government, you know, the British government, the Labour government, and the Tory government before it have been complicit in genocide from bases like RAF Akrotiri, where Keir Starmer went and complimented the troops.

They run the genocide, they send the planes over Gaza, they stream that information live to the Israelis as they’re committing that genocide.

So our government is complicit, and what they’re doing with their complaints is they’re making it illegal for us to oppose it. – Ranjeet Brar, NHS Surgeon

Speakers at the rally urged the GMC to withdraw the appeal; assisting medical professionals should not face professional consequences for raising concerns over civilian suffering in conflict zones.

There’s a clear example here with Dr. Ghassan, where UK law is for Israel, that it is essentially standing up for the rights of a foreign entity, have been pressuring patients, pressuring people to make complaints against Dr. Abu-Sittah, and this is just one example of many other institutions, medical institutions like the Royal Colleges, and even the journals, the medical journals that we publish in, where they’ve been pressured from UK pro-Israel lobby groups to censor and to shut down any form of pro-Palestine activism.

So, I think we’re seeing this now very clearly with Dr. Ghassan, but the reality is it’s much more widespread than any of us think. – Dr Omar Abdel-Mannan, British-Egyptian Pediatric Neurologist

Organizers say they will continue campaigning until the proceedings against Dr. Abu-Sittah come to an end, maintaining that doctors must be free to speak about humanitarian consequences of war without fear or professional repercussions.

Supporters gathered outside the General Medical Council in London to stand behind British Palestinian surgeon Dr. Ghassan Abu-Sittah, accusing the regulators of attempting to silence one of the world’s most prominent war doctors.

Demonstrators say the case is not simply about one medic, but the right of healthcare professionals to speak out on the atrocities of Gaza without professional retaliation.

July 4, 2026 Posted by | Civil Liberties, Ethnic Cleansing, Racism, Zionism, Full Spectrum Dominance, Solidarity and Activism, Video | , , , , | Comments Off on UK and Israel criticized for persecuting anti-genocide advocates

Qatar & Oman Delegations in Iran, Airspace Closed, Israeli Strikes Feared — w/ Prof. Glenn Diesen

Mario Nawfal | July 3, 2026

Elijah Magnier: As Israel’s Losses Mount, a Strategic Reckoning Begins

Dialogue Works | July 2, 2026

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July 3, 2026 Posted by | Video, Wars for Israel | , , , , , , , | Comments Off on Qatar & Oman Delegations in Iran, Airspace Closed, Israeli Strikes Feared — w/ Prof. Glenn Diesen

Israeli spyware used against ex-Greek MEP during probe of illegal surveillance: Report

MEMO | July 3, 2026

Israeli spyware was used to hack the phone of a former Greek member of the European Parliament while he was serving on a committee investigating spyware abuses in Europe, according to a report by Citizen Lab published on Friday, Anadolu reports.

The University of Toronto-based research group said that forensic analysis found Stelios Kouloglou’s iPhone was successfully infected with Pegasus spyware, developed by Israeli company NSO Group, in October 2022 and again the next March.

Kouloglou, a journalist and former MEP, was at the time a substitute member of the European Parliament’s PEGA committee, which was established to investigate the use of Pegasus and equivalent surveillance spyware in EU member states.

Citizen Lab said the infections took place during key periods of PEGA committee activity and could have exposed non-public information, confidential documents, and internal committee deliberations.

“The spyware would have likely captured non-public information about committee activities, possibly breaching EU parliamentary confidentiality and privilege frameworks,” the report said.

The first infection occurred as the committee was preparing hearings on spyware, working on its draft report, and planning fact-finding visits to Greece and the Greek Cypriot Administration. Citizen Lab said Kouloglou’s phone was hacked 10 days before those visits began.

The second infection took place while the committee was engaged in intense discussions over the final drafting process of its report. Kouloglou was in Brussels on March 6-7, 2023, during the period of the infection.

Kouloglou said he was shocked by the findings, describing it as “inconceivable” that a member of the parliamentary committee investigating spyware abuses had himself become a surveillance target, according to Greek news outlet Dnews.

He said he plans to pursue legal action against NSO Group and those responsible for infecting his device, while also raising the issue again through contacts in the European Parliament.

Citizen Lab said the attacks used a “zero-click” exploit, meaning the phone could be compromised without the user opening a link or taking any action.

The group said it was not attributing the attacks to any specific government and found no indication that the Greek government was responsible.

However, it said the first infection overlapped with a previously identified Pegasus campaign targeting Russian and Belarusian-speaking exiled journalists and activists in Europe, suggesting that a Pegasus customer authorized to operate in multiple European countries may have been behind the attack.

Citizen Lab warned that the case posed a serious threat to democratic institutions, saying the hacking could have exposed confidential exchanges among lawmakers and staff, including to parties under investigation by the committee itself.

July 3, 2026 Posted by | Civil Liberties, Deception, Full Spectrum Dominance | , | Comments Off on Israeli spyware used against ex-Greek MEP during probe of illegal surveillance: Report