The Most Revolutionary Act

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The Most Revolutionary Act

September 2001 Interview with Osama bin Laden. Categorically Denies his Involvement in 9/11

Global Research Editor’s Note

We bring to the attention of our readers the following text of Osama bin Laden’s interview in Urdu with Ummat, a Pakistani daily, published in Karachi on September 28, 2001. It was translated into English by the BBC World Monitoring Service and made public on September 29, 2001.

[…]

click here  Ummat  (major Karachi daily)

The interview tends to demystify the Osama bin Laden persona.

In the Unmat interview, Osama bin Laden categorically denies his involvement in the 9/11 attacks.  Bin Laden’s statements in this interview are markedly different from those made in the alleged Osama video tapes.

[…]

It should be noted that on the day preceding the 9/11 attacks, Osama Bin Laden had been admitted for treatment in a Military Hospital in Rawalpindi, Pakistan.

Following is the interview in full detail:

Ummat: You have been accused of involvement in the attacks in New York and Washington. What do you want to say about this? If you are not involved, who might be?

Usamah [Osama bin Laden]: In the name of Allah, the most beneficent, the most merciful. Praise be to Allah, Who is the creator of the whole universe and Who made the earth as an abode for peace, for the whole mankind. Allah is the Sustainer, who sent Prophet Muhammad for our guidance. I am thankful to the Ummat Group of Publications, which gave me the opportunity to convey my viewpoint to the people, particularly the valiant and Momin true Muslim people of Pakistan who refused to believe in lie of the demon.

I have already said that I am not involved in the 11 September attacks in the United States. As a Muslim, I try my best to avoid telling a lie. I had no knowledge of these attacks, nor do I consider the killing of innocent women, children, and other humans as an appreciable act. Islam strictly forbids causing harm to innocent women, children, and other people.

Such a practice is forbidden ever in the course of a battle. It is the United States, which is perpetrating every maltreatment on women, children, and common people of other faiths, particularly the followers of Islam. All that is going on in Palestine for the last 11 months is sufficient to call the wrath of God upon the United States and Israel.

There is also a warning for those Muslim countries, which witnessed all these as a silent spectator. What had earlier been done to the innocent people of Iraq, Chechnya, and Bosnia?

Only one conclusion could be derived from the indifference of the United States and the West to these acts of terror and the patronage of the tyrants by these powers that America is an anti-Islamic power and it is patronizing the anti-Islamic forces. Its friendship with the Muslim countries is just a show, rather deceit. By enticing or intimidating these countries, the United States is forcing them to play a role of its choice. Put a glance all around and you will see that the slaves of the United States are either rulers or enemies of Muslims .

The US has no friends, nor does it want to keep any because the prerequisite of friendship is to come to the level of the friend or consider him at par with you. America does not want to see anyone equal to it. It expects slavery from others. Therefore, other countries are either its slaves or subordinates.

However, our case is different. We have pledged slavery to God Almighty alone and after this pledge there is no possibility to become the slave of someone else. If we do that, it will be disregardful to both our Sustainer and his fellow beings. Most of the world nations upholding their freedom are the religious ones, which are the enemies of United States, or the latter itself considers them as its enemies. Or the countries, which do not agree to become its slaves, such as China, Iran, Libya, Cuba, Syria, and the former Russia as received .

Whoever committed the act of 11 September are not the friends of the American people. I have already said that we are against the American system, not against its people, whereas in these attacks, the common American people have been killed.

According to my information, the death toll is much higher than what the US government has stated. But the Bush administration does not want the panic to spread. The United States should try to trace the perpetrators of these attacks within itself; the people who are a part of the US system, but are dissenting against it. Or those who are working for some other system; persons who want to make the present century as a century of conflict between Islam and Christianity so that their own civilization, nation, country, or ideology could survive. They can be any one, from Russia to Israel and from India to Serbia. In the US itself, there are dozens of well-organized and well-equipped groups, which are capable of causing a large-scale destruction. Then you cannot forget the American Jews, who are annoyed with President Bush ever since the elections in Florida and want to avenge him.

Then there are intelligence agencies in the US, which require billions of dollars worth of funds from the Congress and the government every year. This funding issue was not a big problem till the existence of the former Soviet Union but after that the budget of these agencies has been in danger.

They needed an enemy. So, they first started propaganda against Usamah and Taleban and then this incident happened. You see, the Bush administration approved a budget of 40bn dollars. Where will this huge amount go? It will be provided to the same agencies, which need huge funds and want to exert their importance.

Now they will spend the money for their expansion and for increasing their importance. I will give you an example. Drug smugglers from all over the world are in contact with the US secret agencies. These agencies do not want to eradicate narcotics cultivation and trafficking because their importance will be diminished. The people in the US Drug Enforcement Department are encouraging drug trade so that they could show performance and get millions of dollars worth of budget. General Noriega was made a drug baron by the CIA and, in need, he was made a scapegoat. In the same way, whether it is President Bush or any other US president, they cannot bring Israel to justice for its human rights abuses or to hold it accountable for such crimes. What is this? Is it not that there exists a government within the government in the United Sates? That secret government must be asked as to who made the attacks.

Ummat: A number of world countries have joined the call of the United States for launching an attack on Afghanistan. These also include a number of Muslim countries. Will Al-Qa’idah declare a jihad against these countries as well?

Usamah: I must say that my duty is just to awaken the Muslims; to tell them as to what is good for them and what is not. What does Islam says and what the enemies of Islam want?

Al-Qa’idah was set up to wage a jihad against infidelity, particularly to encounter the onslaught of the infidel countries against the Islamic states. Jihad is the sixth undeclared element of Islam. The first five being the basic holy words of Islam, prayers, fast, pilgrimage to Mecca, and giving alms Every anti-Islamic person is afraid of it. Al-Qa’idah wants to keep this element alive and active and make it part of the daily life of the Muslims. It wants to give it the status of worship. We are not against any Islamic country nor we consider a war against an Islamic country as jihad.

We are in favour of armed jihad only against those infidel countries, which are killing innocent Muslim men, women, and children just because they are Muslims. Supporting the US act is the need of some Muslim countries and the compulsion of others. However, they should think as to what will remain of their religious and moral position if they support the attack of the Christians and the Jews on a Muslim country like Afghanistan. The orders of Islamic shari’ah jurisprudence for such individuals, organizations, and countries are clear and all the scholars of the Muslim brotherhood are unanimous on them. We will do the same, which is being ordered by the Amir ol-Momenin the commander of the faithful Mola Omar and the Islamic scholars. The hearts of the people of Muslim countries are beating with the call of jihad. We are grateful to them.

Ummat: The losses caused in the attacks in New York and Washington have proved that giving an economic blow to the US is not too difficult. US experts admit that a few more such attacks can bring down the American economy. Why is al-Qa’idah not targeting their economic pillars?

Usamah: I have already said that we are not hostile to the United States. We are against the system, which makes other nations slaves of the United States, or forces them to mortgage their political and economic freedom. This system is totally in control of the American Jews, whose first priority is Israel, not the United States. It is simply that the American people are themselves the slaves of the Jews and are forced to live according to the principles and laws laid by them. So, the punishment should reach Israel. In fact, it is Israel, which is giving a blood bath to innocent Muslims and the US is not uttering a single word.

Ummat: Why is harm not caused to the enemies of Islam through other means, apart from the armed struggle? For instance, inciting the Muslims to boycott Western products, banks, shipping lines, and TV channels.

Usamah: The first thing is that Western products could only be boycotted when the Muslim fraternity is fully awakened and organized. Secondly, the Muslim companies should become self-sufficient in producing goods equal to the products of Western companies. Economic boycott of the West is not possible unless economic self-sufficiency is attained and substitute products are brought out. You see that wealth is scattered all across the Muslim world but not a single TV channel has been acquired which can preach Islamic injunctions according to modern requirements and attain an international influence. Muslim traders and philanthropists should make it a point that if the weapon of public opinion is to be used, it is to be kept in the hand. Today’s world is of public opinion and the fates of nations are determined through its pressure. Once the tools for building public opinion are obtained, everything that you asked for can be done.

Ummat: The entire propaganda about your struggle has so far been made by the Western media. But no information is being received from your sources about the network of Al-Qa’idah and its jihadi successes. Would you comment?

Usamah: In fact, the Western media is left with nothing else. It has no other theme to survive for a long time. Then we have many other things to do. The struggle for jihad and the successes are for the sake of Allah and not to annoy His bondsmen. Our silence is our real propaganda. Rejections, explanations, or corrigendum only waste your time and through them, the enemy wants you to engage in things which are not of use to you. These things are pulling you away from your cause.

The Western media is unleashing such a baseless propaganda, which make us surprise but it reflects on what is in their hearts and gradually they themselves become captive of this propaganda. They become afraid of it and begin to cause harm to themselves. Terror is the most dreaded weapon in modern age and the Western media is mercilessly using it against its own people. It can add fear and helplessness in the psyche of the people of Europe and the United States. It means that what the enemies of the United States cannot do, its media is doing that. You can understand as to what will be the performance of the nation in a war, which suffers from fear and helplessness.

Ummat: What will the impact of the freeze of al-Qa’idah accounts by the US?

Usamah: God opens up ways for those who work for Him. Freezing of accounts will not make any difference for Al-Qa’idah or other jihad groups. With the grace of Allah, al-Qa’idah has more than three such alternative financial systems, which are all separate and totally independent from each other. This system is operating under the patronage of those who love jihad. What to say of the United States, even the combined world cannot budge these people from their path.

These people are not in hundreds but in thousands and millions. Al-Qa’idah comprises of such modern educated youths who are aware of the cracks inside the Western financial system as they are aware of the lines in their hands. These are the very flaws of the Western fiscal system, which are becoming a noose for it and this system could not recuperate in spite of the passage of so many days.

Ummat: Are there other safe areas other than Afghanistan, where you can continue jihad?

Usamah: There are areas in all parts of the world where strong jihadi forces are present, from Indonesia to Algeria, from Kabul to Chechnya, from Bosnia to Sudan, and from Burma to Kashmir. Then it is not the problem of my person. I am helpless fellowman of God, constantly in the fear of my accountability before God. It is not the question of Usamah but of Islam and, in Islam too, of jihad. Thanks to God, those waging a jihad can walk today with their heads raised. Jihad was still present when there was no Usamah and it will remain as such even when Usamah is no longer there. Allah opens up ways and creates loves in the hearts of people for those who walk on the path of Allah with their lives, property, and children. Believe it, through jihad, a man gets everything he desires. And the biggest desire of a Muslim is the after life. Martyrdom is the shortest way of attaining an eternal life.

Ummat: What do you say about the Pakistan government policy on Afghanistan attack?

Usamah: We are thankful to the Momin and valiant people of Pakistan who erected a blockade in front of the wrong forces and stood in the first file of battle. Pakistan is a great hope for the Islamic brotherhood. Its people are awakened, organized, and rich in the spirit of faith. They backed Afghanistan in its war against the Soviet Union and extended every help to the mojahedin and the Afghan people. Then these are the same Pakistanis who are standing shoulder by shoulder with the Taleban. If such people emerge in just two countries, the domination of the West will diminish in a matter of days. Our hearts beat with Pakistan and, God forbid, if a difficult time comes we will protect it with our blood. Pakistan is sacred for us like a place of worship. We are the people of jihad and fighting for the defence of Pakistan is the best of all jihads to us. It does not matter for us as to who rules Pakistan. The important thing is that the spirit of jihad is alive and stronger in the hearts of the Pakistani people.

End of Interview

 

[Copyright Ummat in Urdu, BBC translation in English, 2001]

 

13 Things Your Pediatrician Was Trained Not to Tell You

Unbekming
10 Sept 2026

“Nothing bad should be said about any vaccine.”¹ That is what Suzanne Humphries, a board-certified nephrologist, was taught during her American medical training. Vaccines are administered on schedule. Adverse conversation was not encouraged. It was actively closed down.

[…]


1. The Cord Cut Before the Blood Finished Moving (birth)

A newborn’s blood volume is meant to be topped off from the placenta in the minutes after birth. When the cord is left intact and pulsing, roughly a third of the baby’s total blood supply, along with the iron that supply carries, transfers across before the placenta is expelled. That iron is the reserve intended to carry the child through the first six months of life.

The standard hospital practice throughout the late twentieth century was to clamp within seconds. The World Health Organization now recommends waiting at least one minute. The American College of Obstetricians and Gynecologists came around in 2017. Most hospital deliveries in the United States still clamp early, driven by workflow, the neonatal warmer schedule, and the syringe already on the tray.

[…]

Six months later, that same pediatrician will run an iron level, note the low result, and prescribe supplementation. The low reading she treats was produced by the system at birth. She is not trained to draw the line between the two events. She is trained to run the number and write the script.

[…]


2. The Vitamin K Injection (first hours)

Within hours of birth, the newborn receives an intramuscular injection of phytonadione, the compound sold as vitamin K1. The dose is one milligram. Breast milk carries roughly one to two micrograms of phytonadione per liter, and a newborn’s colostrum intake on day one delivers a fraction of a microgram; the injection is thousands of times that dose, and the published pediatric literature confirms that plasma phytonadione levels for two weeks after the shot run one to two thousand times higher than normal adult values. The injection also contains benzyl alcohol, polysorbate 80, and propylene glycol as excipients. T

[…]

The condition exists. What is not explained is why. Newborn phytonadione levels are low at birth by design; the compound is produced by the gut bacteria that colonize the infant’s digestive tract in the first days, and levels rise on the biological schedule the infant’s body follows. Levels are further supported by the maternal transfer that continues through breastfeeding. The “deficiency” the injection corrects is the state a healthy newborn is meant to occupy for the first days of life while the gut ecology establishes itself.⁶

The bleeding events the injection is designed to prevent cluster in infants who have been subjected to the standard hospital birth sequence: early cord clamping, which strips the placental transfusion of clotting factors; maternal medications passed through delivery; the injection itself as a source of tissue injury; and, in male infants, circumcision. The intervention creates the conditions in which bleeding becomes more likely, then presents itself as the solution to the problem it has helped produce.

Two forms of the shot exist. The oral form is available in some countries and delivers a smaller dose across three administrations in the first weeks of life. The intramuscular form is the American standard. The intramuscular form has been associated in the published literature with elevated rates of childhood cancer, a finding disputed by subsequent industry-funded studies but never resolved. The oral form does not appear in that literature.⁷

[…]


3. The Hepatitis B Shot Before the First Feed (first day)

Hepatitis B, in the establishment’s account, is transmitted through blood-to-blood contact or sexual contact. In the United States it is given as an injection to every newborn within twenty-four hours of birth, regardless of the mother’s status.


4. The Circumstraint (first days)

Boys born in American hospitals are commonly circumcised within the first forty-eight hours of life. The procedure is elective, performed on healthy tissue, without therapeutic indication. The device most commonly used to hold the infant during the procedure is called the Circumstraint, a plastic form that immobilizes the baby’s arms and legs so the surgeon can work.

Forrest Maready has written on what happens inside the infant’s body during this event.¹³ Three triggers activate the dorsal vagal complex simultaneously: the injected local anesthetic registers as chemical intrusion, the incision as tissue injury, and the strap and plastic form as restraint.

[…]

The procedure requires written consent. It does not require informed consent. Parents are not shown the Circumstraint, or what dorsal vagal shutdown looks like. They are told the boy will not remember.

[…]

Your pediatrician was not trained in polyvagal theory. The circumcision was billed separately, performed by a different practitioner, and by the time she sees the child for the first well-baby visit, the file is closed and the incision has healed.


5. The Formula Sample in the Discharge Bag (first weeks)

Breast milk is more than food. It is a continuation of the mother’s biology into the infant. It delivers living stem cells, signalling molecules, protective proteins, and dozens of maternal components the infant’s biology integrates into its own.¹⁴ Colostrum in the first days carries a concentration of maternal material no manufactured product can replicate. The list of components identified in breast milk grows every year.

[…]

6. The Growth Chart Announcement (every visit)

At every visit, the baby is weighed and measured. The numbers are plotted against a curve. The pediatrician announces the percentile. Anything below the fiftieth is met with concern. Anything below the tenth triggers supplementation, formula, referrals, and repeat visits.

The curve is a statistical instrument. It plots where a population’s babies actually fell, not where healthy babies should fall. The reference standards against which most American pediatricians still work were built substantially on formula-fed populations, until the World Health Organization revised its curves in 2006 based on breastfed infants. A breastfed baby, whose weight-gain curve flattens naturally after four to six months, tracks below the older references and appears to be failing. The formula-fed baby was the standard against which the breastfed baby was measured and labeled as failing to thrive.

[…]


7. The Iron Drops at Six Months (six months)

The four-month or six-month iron level comes back low. The pediatrician prescribes ferrous sulfate drops or recommends iron-fortified cereal. The parent complies. The drops stain the baby’s teeth, alter the stool, and are frequently spit up. The parent gives them anyway because the pediatrician said the number was low.

The number was low because the placenta was cut early. The reference range was developed on infants who were also cut early. The whole system, from delivery-room workflow to the reference range on the lab printout, was calibrated around interventions that removed the natural iron reserve at birth.


8. Amoxicillin for the Ear (infancy onward)

The child has an earache. The pediatrician looks in the ear, notes the red drum, and writes a script for amoxicillin. Ten days. The ear improves. Three weeks later, the ear is red again. Another course. By eighteen months, the child has been on four rounds of antibiotics. The referral to ENT for tubes is in the file.

A 1994 study in Annals of Allergy identified food allergy in 78 percent of a series of 104 children with recurrent middle-ear fluid. Of the food-allergic group, 86 percent showed significant reduction on a sixteen-week elimination diet; when the offending foods were reintroduced, 94 percent recurred. The common offenders were cow’s milk, eggs, wheat, corn, soy, and peanuts.¹⁶ Children with undiagnosed cow’s milk allergy are roughly twice as likely to have recurrent ear problems. The ENT specialist David Hurst has spent his career documenting that allergy is the primary driver of chronic middle-ear fluid, and that aggressive allergy management resolves most cases.¹⁷

[…]


9. The Autism Screening at Eighteen Months (eighteen to twenty-four months)

The M-CHAT is administered at the eighteen-month and twenty-four-month well-child visits. It is a screening questionnaire designed to catch signs of autism early. Parents whose children screen positive are referred for further evaluation.

By eighteen months, an American child following the CDC schedule has received over twenty vaccine doses. The MMR is typically administered at twelve to fifteen months. The pattern of parental accounts documented across the literature is consistent: the child was developing normally, received the shots at fifteen to eighteen months, and regressed.²⁰

[…]


10. The Tonsillectomy Recommendation (early childhood)

The child has recurrent throat inflammation, or the tonsils appear enlarged, or the sleep is poor. The pediatrician refers to ENT. The ENT recommends removal. The parents comply.

During the American polio era, fifty to eighty percent of middle- and upper-class American children were tonsillectomized. Anderson’s 1943 Utah data showed that poliomyelitis was more than 2.5 times as common in tonsillectomized children. Bulbar polio, the form that paralyzed the muscles of breathing and swallowing, was sixteen times more common. Forty-three percent of the bulbar and bulbospinal cases had been preceded by a tonsillectomy within thirty days.²⁴ After the connection surfaced in the medical literature, tonsillectomy rates collapsed. The procedure never recovered its earlier prevalence, though it remains common enough to be a routine referral.

The tonsils are lymphatic tissue. They are part of the body’s cleansing and repair infrastructure, positioned at the entry point of the digestive and respiratory tracts to sample what comes in and to house the response.


11. The Stimulant Prescription (school age)

The teacher flags the boy. His mother takes him to the pediatrician. A screening tool is administered. The prescription follows. Ritalin, Adderall, Vyvanse, Concerta.

The DSM criteria for ADHD are behavioral. There is no biomarker.

[…]

The condition is defined by the behavior and validated by the response to the stimulant, which by design produces focus and compliance in almost any child regardless of underlying condition.

Maready has proposed that the behavioral pattern derives from damage to a small brainstem structure called the locus coeruleus, which regulates the release of norepinephrine and mediates the fight-or-flight response.²⁶ Damage produces hypersensitivity and continuous norepinephrine release. The child is locked in a low-grade panic state. He cannot sit still because his body is preparing for a threat that never resolves. The gut problems that frequently accompany the ADHD presentation follow from the same diversion of resources away from digestion. Many parents notice that their child’s behavior improves markedly during a fever, which fits the same mechanism: the locus coeruleus diverts its norepinephrine output to raising body temperature, giving the child a temporary respite from the constant stress signal.²⁷

The metals implicated in the damage, in Maready’s account, are the aluminum-based adjuvants injected in the leg during infancy and transported by the lymphatic system toward the brainstem.²⁸ Studies have documented elevated aluminum in the hair of children diagnosed with hyperactivity.


12. The SSRI for the Teenager (adolescence)

The teenage girl is depressed. Her pediatrician writes the SSRI. American pediatric and family practice are the frontline prescribers of adolescent SSRIs; referral to a child psychiatrist happens only for complex cases. The FDA’s own black-box warning, added in 2004, states that these compounds increase suicidal ideation in children and adolescents. The warning appears on the label. It is rarely raised in the conversation before the script is signed.


13. The Gardasil Series (eleven to twelve)

The eleven-year-old girl is offered the HPV vaccine at her pediatric well-visit; American pediatric care runs through adolescence, and the HPV series is a scheduled pediatric-office item. In many practices, the shot is bundled with the meningococcal and Tdap boosters at the same visit, an arrangement the Advisory Committee on Immunization Practices (ACIP) recommends explicitly to improve series completion.³⁰ The practice’s incentive is to have the teenager walk out with all three.

The clinical trials submitted for HPV vaccine approval did not use saline as the placebo. The comparator was the aluminum adjuvant, which produces its own inflammatory and neurological effects.³¹ The trials measured precancerous lesions, not cervical cancer, which develops on a timeline decades longer than the trials ran. The insert states that the product has not been evaluated for carcinogenicity or genotoxicity.³²

The injury patterns reported after HPV vaccination include postural orthostatic tachycardia syndrome, seizures, chronic fatigue, cognitive dysfunction, motor symptoms, and premature ovarian failure.

[…]

Via https://www.unbekoming.com/p/13-things-your-pediatrician-was-trained

The Vitamin K Injection

Every U.S. newborn is offered a shot in the leg in the first hour of life. Parents are rarely told the shot exists until the moment it is about to be given.

The new paperback is out today. It examines that shot.

What’s in the book

Twenty-seven chapters walk through what the vitamin K injection actually is, what it contains, what the manufacturers themselves warn against, what the studies did and didn’t find, and where the current framework came from.

The intervention itself. The three products currently in use in English-speaking countries — the U.S. Hospira formulation with its polyoxyethylated castor oil and benzyl alcohol preservative, the UK Konakion MM Paediatric with its glycocholic-acid mixed-micelle vehicle, and the Australian Konakion MM Paediatric with its lecithin base. What each carries alongside the vitamin K itself. The depot vehicle that keeps the injection releasing into the baby’s tissue for two months after the needle comes out. The aluminum contamination the manufacturer discloses without context. The peanut allergy pathway the mainstream literature acknowledges but does not track.

The manufacturer’s own warnings. Every current package insert opens with a boxed warning against the exact route of administration hospitals universally use. Every insert lists a set of adverse reactions — anaphylaxis, cyanosis, gasping syndrome, skin necrosis, cardiovascular collapse — that the doctors administering the shot are largely unaware of and that parents are never shown.

The history. A 1961 AAP recommendation set by a small committee that did not test what it was recommending. A 1985 quiet shift from targeted to universal injection. A 1992 cancer signal from a large UK cohort study that was dismissed rather than investigated. The menadione (K3) disaster that hospitals eventually withdrew — but only by switching products, never by pausing to ask whether the intervention itself was needed. Dam and Doisy’s 1943 Nobel, awarded for work in starved chickens, later used to justify universal injection of healthy newborns.

The alternatives. The oral vitamin K protocols in continuous use in the Netherlands, Germany, Switzerland, and Denmark. Their dosing schedules, their VKDB failure rates, their published surveillance data. Maternal supplementation as a route the doctors could offer but don’t. The physiologic support at birth that most modern maternity practice has already adopted for other reasons but has never been asked to interact with the shot.

The system machinery. The standing-order framework that bypasses individual consent. What refusal actually costs the parent, and what it usually doesn’t cost the baby. The circumcision-clotting interaction that turns one cultural habit into justification for another.

Two personal stories. A father’s account of what happened after his son’s shot. A mother’s account of what changed the week the injection was administered.

Two practical tools. A checklist of questions for the practitioner conversation. A country-by-country reference of the oral protocols with dosing, timing, and documented outcomes.

And at the end of every chapter, a short section titled How to Explain It to a Six-Year-Old.

If you’re picking one up, pick two

The natural pigeon pair for The Vitamin K Injection is The Unvaccinated: What a Forbidden Comparison Reveals About the True Cost of Vaccination. The two examine the same institutional logic from different angles. Vitamin K is the first injection most newborns receive; the childhood schedule follows. Both document what the mainstream literature won’t compare, won’t study, and won’t offer as choice.

The Unvaccinated
[…]

Medicine Has Forgotten How to Touch the Patient

Medicine Has Forgotten How to Touch the Patient

By

September 13, 2026

When was the last time your doctor actually examined you? I do not mean when someone checked your blood pressure, copied your medication list, looked at your laboratory results, or listened briefly through a shirt before returning to the computer. I mean examined you. Looked at you. Watched you breathe. Felt your pulse. Looked at your eyes. Examined your neck. Listened carefully to your heart and lungs. Palpated your abdomen. Watched you walk. Noticed the color of your skin, the movement of your hands, the expression on your face, and the thousand other small pieces of information that a human body offers to someone who has learned how to observe it.

For most of the history of medicine, this was not an optional ritual performed before ordering the “real tests.” This was medicine. Today, increasingly, it is treated as something quaint, inefficient, or unnecessary.

I have spent most of my professional life taking care of very sick people. Critical care is one of the most technologically intensive areas of medicine ever created. I love technology. I have watched mechanical ventilators breathe for patients who could no longer breathe for themselves. I have used ultrasound, CT imaging, sophisticated hemodynamic monitoring, extracorporeal technologies, molecular diagnostics, and laboratory measurements that physicians a generation before me could only have dreamed about.

I would never want to return to a world without these tools. But after decades at the bedside, I have also learned something that becomes more obvious, not less, with experience: technology is most powerful when it extends the physician’s senses. It becomes dangerous when it persuades the physician that those senses are no longer necessary.

The Patient Before the Data

Experienced clinicians understand something that is remarkably difficult to teach in a lecture hall or classroom. Sometimes you walk into a room and know immediately that something is wrong. You may not yet know what it is, but you know it before the laboratory does. The patient is breathing differently. His skin looks different. She answers a question a fraction of a second more slowly than she did several hours earlier. Posture, speech, facial expression, respiratory effort, or level of attention changes. None of these observations is magical. They are data, collected by a biological instrument trained through thousands and thousands of encounters: the physician.

When I round in an intensive care unit (ICU), I can learn an enormous amount before touching the computer. I can see whether a patient is fighting the ventilator. I can hear secretions from the doorway. I can see accessory muscles contracting. I can recognize when someone who looked reasonably comfortable earlier suddenly looks exhausted. I can see peripheral perfusion, diaphoresis, agitation, abdominal distension, or a subtle change in mental status. None of this means I should ignore the arterial blood gas, the chest radiograph, the CT scan, or the monitor. Of course I need them. The mistake is believing that because those measurements are more technologically sophisticated, they are necessarily more real than what is happening directly in front of me.

Medicine once began with the patient and proceeded toward testing. Increasingly, it begins with testing and eventually works its way back toward the patient. Abraham Verghese and colleagues have described this inversion of the diagnostic process, in which clinicians may encounter an image or electronic representation of a patient before encountering the patient himself. That change sounds subtle. It is not. Once the CT scan, laboratory panel, consultant note, medication list, and previous diagnoses have entered our minds, we no longer approach the patient without preconceptions. The data have already told us what we are supposed to see.

This is one reason the physical examination should never be reduced to nostalgia. Its value is not that physicians once carried black bags and made house calls. Its value is epistemological. It provides an independent stream of information. The history and physical examination can support what the tests tell us, but they can also contradict them. That contradiction is often where important medicine begins. A normal number should make us reconsider an abnormal observation, but an abnormal observation should also make us reconsider a normal number.

The Screen between Us

Something extraordinary happened to the architecture of the medical encounter. The physician and patient used to face each other. Today, they frequently face a computer.

A widely cited time-and-motion study of ambulatory physicians found that during the clinic day physicians spent approximately 27 percent of their time in direct clinical face time with patients and nearly half their time on electronic health records and desk work. For every hour of direct clinical face time, physicians spent almost two additional hours on electronic documentation and related desk activities during the workday. The electronic medical record was introduced as a tool for storing information. Somewhere along the way, the physician became one of the tools used to feed the electronic medical record.

This has consequences that go well beyond physician irritation or burnout. Attention is a finite resource. When I am looking at a screen, I am not fully looking at you. When I am clicking boxes, reconciling lists, responding to alerts, and documenting everything necessary to satisfy billing, regulatory, legal, and institutional requirements, I am performing work. But that work is not the same thing as observing a patient. We have confused documentation of care with care itself.

The modern medical record can create a remarkable illusion of precision. A note may contain a beautifully populated physical examination with normal findings listed across multiple organ systems. Anyone who has practiced modern medicine knows the uncomfortable truth: sometimes the completeness of the electronic examination exceeds the completeness of the actual one. Elder and colleagues warned years ago about examinations transformed by templates and drop-down boxes into records that may look more impressive than what truly occurred at the bedside.[2] The computer makes it possible to document fifteen normal observations in seconds. Unfortunately, it cannot guarantee that anyone actually made those observations.

The irony is striking. Never in history have physicians possessed more information about their patients, yet we may sometimes know them less. We know their hemoglobin from three years ago. We can review every medication prescribed by another physician. We can scroll through imaging reports, genetic data, vaccination histories, risk scores, and dozens of laboratory trends. We may possess thousands of data points about a human being who has received only a few minutes of our undivided attention.

The Physical Examination Is Not Primitive Technology

There is a tendency to speak about the physical examination as though it were the horse and buggy of diagnosis, something admirable in its time but sensibly replaced by superior machinery. That misunderstands what examination is. A physical finding is simply another diagnostic test. It has sensitivity, specificity, likelihood ratios, false positives, and false negatives, just like laboratory measurements and imaging studies. The Rational Clinical Examination movement made precisely this point decades ago, arguing that clinical findings should be subjected to the same rigorous evaluation applied to other diagnostic tools.

Some physical findings are poor. Some are excellent. Some things we were taught generations ago probably deserve to disappear. There is no virtue in preserving an examination maneuver merely because an old professor taught it to us. Evidence-based medicine should apply to the stethoscope as rigorously as it applies to an MRI scanner. But there is a tremendous difference between saying that certain bedside findings are unreliable and concluding that bedside observation itself has become obsolete.

The evidence also suggests that inadequate examination can cause harm. In one collection of cases involving physical-examination failures, missed or delayed diagnoses were common, as were unnecessary testing and treatment. Reviews of diagnostic error continue to identify deficiencies in history taking and physical examination as important contributors. These are not arguments against technology. They are arguments against voluntarily throwing away information before making decisions.

Consider something as simple as breathing. A pulse oximeter gives me a number, and that number can be enormously useful. But it does not tell me everything I learn by watching someone breathe. Two patients can have identical oxygen saturations while one is resting comfortably and the other is approaching respiratory failure. Respiratory rate, depth, pattern, accessory muscle use, paradoxical movement, ability to speak, mental status, and fatigue matter. Anyone who has managed respiratory failure has seen a patient whose monitor still looked reassuring while the patient absolutely did not.

The same is true throughout medicine. An echocardiogram can characterize cardiac anatomy better than my stethoscope ever will. Still, jugular venous distension, cool extremities, edema, diaphoresis, or altered mentation may tell me instantly that circulation is failing. A CT scan can show me an abdomen in exquisite detail, but it cannot substitute for knowing whether that abdomen has suddenly become rigid and exquisitely tender. Technology provides resolution. Examination provides context. Good medicine requires both.

We Are Losing the Teachers Too

Skills disappear surprisingly quickly when institutions stop rewarding them. Medical students enter training fascinated by physical diagnosis. They buy stethoscopes, learn cardiac sounds, practice neurologic examinations, and struggle to distinguish normal from abnormal findings. Then they enter the clinical environment and observe what the system actually values. They watch residents review laboratory values outside the room. They watch teams conduct portions of rounds around computers. They learn that ordering a test is often faster than finding someone who can teach them how to elicit a finding.

They discover that no billing system awards extra productivity points because a physician spent ten additional minutes teaching a student how to examine jugular venous pressure. Eventually they absorb the real curriculum of modern medicine: what the institution measures matters, and what it does not measure becomes optional.

Research has documented deficiencies in physical examination skills among medical trainees and has shown that bedside teaching itself has declined. Particularly troubling is evidence that greater time in training does not automatically produce better examination technique. One direct-observation study found physical examination technique correlated with recognition of clinical signs, differential diagnosis, and clinical judgment, yet performance actually deteriorated during internship. That should concern us. We may be creating a system in which physicians accumulate more medical knowledge while simultaneously losing some of the mechanisms through which they apply that knowledge to real human beings.

Clinical medicine has always depended on apprenticeship. You can learn the physiology of aortic stenosis from a book. Still, there is something different about standing beside an experienced cardiologist who places your stethoscope exactly where the murmur is clearest and tells you what to listen for. You can memorize the manifestations of cirrhosis, but you remember them differently after someone shows you spider angiomas, ascites, muscle wasting, and asterixis in a real patient. You can watch a thousand videos about respiratory distress, but watching an experienced intensivist recognize impending fatigue at the bedside teaches something that no multiple-choice examination can measure.

Once one generation loses those skills, the next generation has nobody to teach them. That is how knowledge disappears from a profession. Not through a decree announcing that the skill is forbidden, but through gradual neglect until eventually nobody remembers that it mattered.

Touch Is Also Communication

Another element of the physical examination is harder to quantify, and perhaps for that reason easier for modern medicine to discount. Examination is a form of human communication. When a frightened patient comes to see a physician, he does not simply want information. He wants to know that someone competent has assessed him. There is a difference between saying, “Your CT scan looks fine,” and sitting beside the patient, listening to his story, examining the area that hurts, and then explaining why the findings are reassuring. The diagnostic conclusion may be identical. The human experience is not.

[…]

Via https://brownstone.org/articles/medicine-has-forgotten-how-to-touch-the-patient/

Trump blames fuel price spike on Zelensky

Trump blames fuel price spike on Zelensky

RT

13 Sep, 2026 

US diesel prices have hit a new record, soaring past $6 per gallon this week

US President Donald Trump has blamed Ukrainian leader Vladimir Zelensky for the ongoing diesel price shock, saying it was a result of Kiev’s attacks on Russian refineries.

The national average price of diesel hit more than $6 per gallon on Friday, up from approximately $5.85 last week. The price has climbed some 60% compared to the same period last year, when diesel fuel cost some $3.71 per gallon. Market experts have mainly linked the hike to the conflict in the Middle East and the reignited hostilities between the US and Iran, which have prompted a renewed rise in crude oil prices.

Trump, however, insisted that this was not the case, telling reporters while on a visit to Ireland that the diesel price spike was actually related to the Russia-Ukraine conflict. The US president said he had already raised the issue with the Ukrainian leader and told him to stop attacking diesel production in Russia.

“Zelensky has to do one thing. He has to stop knocking out diesel fuel in Russia. Let him go after targets, but not diesel fuel, because he’s causing a shortage of diesel,” Trump asserted, adding that “this isn’t done by the Middle East.”

In recent months, Ukraine has repeatedly attacked oil refineries and other petroleum installations in Russia. While the strikes have caused fuel shortages and price hikes across multiple Russian regions, the attacks have primarily affected gasoline, while the diesel supply has remained largely undisrupted.

To battle the shortages, the Russian government introduced a temporary ban on exporting gasoline and diesel, as well as other petroleum products. The diesel exports ban was first introduced early this year and extended to gasoline producers in July. The diesel ban is currently in effect until the end of September, yet it is likely to be extended further.

Diesel fuel has been more expensive in the US than gasoline for decades and has previously shown tendencies to rise in price at a faster pace. It is integral to the food supply chain, since it is used to power agricultural machines as well as the cargo trucks and trains which deliver the produce. The cost of fuel accounts for between 15% and 30% of the total cost of food in the US, according to various estimates, and the ongoing hike is bound to affect consumer prices.

[…]

Via https://www.rt.com/news/645651-trump-zelensky-diesel-price/

Former CDC Scientist Whose Studies Were Used to Debunk Vaccine-Autism Link Will Plead Guilty

poul thorsen and words "plea guilty"

A former Centers for Disease Control and Prevention (CDC) scientist who played a crucial role in research rebutting any link between vaccines and autism is expected to plead guilty next week to wire fraud and money laundering.

Poul Thorsen, 65, is finalizing a plea deal with prosecutors relating to charges stemming from a 2011 federal indictment, Nathan Kitchens, assistant U.S. Attorney for the Northern District of Georgia, told The Defender.

Thorsen, who began working for the CDC in the late 1990s, faces two counts of wire fraud and nine counts of money laundering related to over $1 million in CDC grant money. The funds were earmarked for autism and public health research, but Thorsen allegedly used them to buy a home, two cars and a motorcycle.

Kitchens declined to comment on whether Thorsen will plead guilty to all or some of the charges.

Thorsen has been held in federal custody without bail since his extradition from Germany to the U.S. in May. The case is being heard at a federal court in Georgia, where the CDC is headquartered.

Researcher James Grundvig, the parent of a child with autism who was vaccine-injured, called the expected guilty plea “a very big deal.”

Grundvig, who wrote “Master Manipulator: The Explosive True Story of Fraud, Embezzlement, and Government Betrayal at the CDC,” which focused on the Thorsen case, praised U.S. Health Secretary Robert F. Kennedy Jr. for extraditing Thorsen “in record speed.”

He said Thorsen likely understands that the FBI and U.S. Department of Justice have “all the goods” to prosecute him.

“I guess Thorsen’s realizing, since he’s in American jail already and has no chance for bail, he might as well make a plea deal,” Grundvig said.

Dr. Dave Weldon, a physician and Republican member of the U.S. House of Representatives between 1994 and 2009 — and who President Donald Trump nominated to lead the CDC in late 2024 before retracting his nomination in March 2025 — welcomed the plea agreement but said it isn’t enough.

“It would be a miscarriage of justice if a plea deal failed to include a thorough investigation of allegations of scientific fraud,” Weldon said.

Danish independent vaccine safety researcher Vibeke Manniche, M.D., Ph.D., said some of the federal funds Thorsen is said to have misused may have been intended for vaccine-autism studies. Manniche said the guilty plea calls Thorsen’s research into question.

“An obvious question is whether he also has been cheating with data to achieve the results he sought,” Manniche said. “That we don’t know. A good rule in gold-standard science is replication, and it would be wise, for so many reasons, to replicate his work,” independently of the institutions Thorsen had been affiliated with.

Grundvig noted that the Thorsen indictment included unnamed co-conspirators, suggesting that the investigation may implicate more people — and also the controversial autism research that Thorsen helped publish in 2002 and 2003 that was cited as proof of no link between vaccines and autism.

“I think that’s going to be the second part of the story,” Grundvig said. “It could be an avalanche of bad news for both pharma and the CDC.”

Thorsen studies cited in dismissing over 5,000 vaccine injury claims

Despite questions around how those studies were conducted, the Madsen-Thorsen papers were used in 2011 to dismiss over 5,000 claims filed by the parents of autistic, vaccine-injured children. The claims were part of the Omnibus Autism Proceeding pending before the Vaccine Injury Compensation Program.

In “Master Manipulator,” Grundvig — whose son’s case was one of the claims dismissed as a result of Thorsen’s research — described Thorsen as “a world-class villain whose manipulation of health data gave CDC and big pharma what they wanted: a report clearing thimerosal of any possible role in the autism crisis.”

According to Weldon:

“The real crime is not absconding with research dollars, but unresolved allegations around his research which served as the basis for the CDC and the U.S. government dismissing vaccine injury claims by thousands of injured children. These actions set back vaccine safety research by more than two decades.”

Grundvig suggested the Thorsen investigation and his guilty plea may call into question the dismissal of the omnibus cases, as it would “then make all of those vaccine omnibus proceedings completely fraudulent because it was based on a fraud, and that should reopen the cases.”

Hooker, whose omnibus claim for his son was also dismissed, said Thorsen likely didn’t act alone in misusing federal money or misrepresenting vaccine-autism research — and that the role of some of his key collaborators should be examined.

“There should be a separate investigation against Dr. Diana Schendel, who was Thorsen’s direct grant supervisor and lover and approved all of his invoices for expenditures from his CDC grant money. Dr. Schendel undoubtedly knew of Thorsen’s activities but did not report them to the authorities and could have spent some of the stolen grant money as well,” Hooker said.

Schendel maintained an inappropriate romantic relationship with Thorsen and later accepted a position at Denmark’s Aarhus University to lead autism research there. She remains employed at Aarhus University — and at Drexel University — today.

Thorsen continued to live in Denmark for years after the 2011 U.S. indictment. He worked there as a gynecologist despite an extradition treaty between the two countries and an INTERPOL warrant for his arrest.

Hooker added:

“Other co-conspirators who knew of the inappropriate relationship between Thorsen and Schendel over the seven-year grant history at CDC include Coleen Boyle, Ph.D., former director of the National Center for Birth Defects and Developmental Disabilities), and Dr. Marshalyn Yeargin-Allsop, former branch chief of the Developmental Disabilities Branch at the CDC.

“These individuals at a minimum should be brought in for questioning. Both have also been implicated in the MMR-autism fraud from the DeStefano et al. 2004 paper, where data showing a strong relationship between MMR timing and autism in Black boys was illegally destroyed.”

Thorsen’s vaccine-autism studies full of ‘irregularities’

When he first joined the CDC as a visiting scientist, Thorsen’s research focused on birth defects and developmental disabilities.

However, by the early 2000s, Thorsen shifted his focus to autism research. His work in this area left a strong imprint, fueling future narratives that autism isn’t linked to vaccines.

According to a 2017 report by the World Mercury Project — predecessor to Children’s Health Defense (CHD) — Thorsen’s influence on U.S. vaccine projects and policies “is extensive” because his studies were used to dismiss a possible link between vaccines and autism.

One of the most influential studies became known as the “Madsen study,” a population-based study of the measles-mumps-rubella (MMR) vaccine and autism.

Published in 2002 in The New England Journal of Medicine and co-authored by Thorsen, the Madsen study concluded that there is “strong evidence against the hypothesis that MMR vaccination causes autism.”

However, according to the 2017 World Mercury Project report, the Madsen study was “flawed” from the outset because the researchers reviewed clinical records of only 40 of the 316 children who had autism in the study’s cohort.

A peer-reviewed analysis published last year cast further doubt on the study’s conclusions.

In 2003, Madsen and Thorsen co-authored another influential study, published in Pediatrics, the journal of the American Academy of Pediatrics. The study did “not support a correlation between thimerosal-containing vaccines and the incidence of autism.”

Thimerosal is a mercury-based adjuvant used in some vaccines, which some scientists and advocates for people with autism have suggested may trigger autism.

Brian Hooker, Ph.D., CHD’s chief scientific officer, said there are “numerous data irregularities” in the Thorsen studies.

In their critique of the 2002 paper, Hooker and Karl Jablonowski, Ph.D., CHD senior research scientist, found significant errors in the paper. They concluded the study’s unadjusted results “do not support rejecting the causal link” between the MMR vaccine and autism.

In a critique of the 2003 Madsen-Thorsen study, Hooker and researcher Jeffrey Allen Trelka concluded that the study’s findings “may have been skewed by participant selection and changes in diagnostic groupings.”

Other critiques of the 2002 and 2003 studies raised concerns about ethical considerations. Both studies relied on Danish population data. According to the 2017 World Mercury Project report, the studies bypassed ethical reviews required for this category of research, as required by federal law.

When the CDC discovered Thorsen hadn’t obtained the required ethics approvals, the agency didn’t report the errors, and the studies weren’t retracted. Instead, CDC officials engaged in a cover-up, the 2017 report states.

“Given these irregularities, Thorsen should also be under investigation for data fraud as he clearly withheld data and could have altered data” from Danish official sources, Hooker told The Defender.

Manniche said that if it is proven Thorsen tampered with the data in his studies, it would be a “terrible tragedy,” because “parents were told that the MMR vaccine was safe and sound and that it couldn’t harm the child.”

As of July 31, there were 1,931 reports claiming onset of autism or autism spectrum disorder following MMR vaccination contained within the federally run Vaccine Adverse Event Reporting System (VAERS).

Will Thorsen sing?

Grundvig suggested that, as part of his plea agreement with prosecutors, Thorsen may have an incentive to provide testimony or information targeting other CDC figures.

“Thorsen’s 65 years old, born in 1961 … does he want to die in an American jail?” Grundvig asked. “I don’t think so. So, I think he wants to make, and will make, a plea deal. The only way he’s going to make a plea deal is with someone like Kennedy and maybe others in the Department of Justice that look at a bigger case,” Grundvig said.

Grundvig suggested this “bigger case” may involve the Racketeer Influenced and Corrupt Organizations Act or RICO Act.

“There’s a bigger fraud involved than just stealing money, and I think it goes back to the vaccines, it goes back to the studies that the CDC cooked up,” potentially implicating Schendel and Madsen.

“Will he be used as a star witness against the CDC old guard and all of the shenanigans that went on massaging of science, of science papers, influence on Pediatrics and other journals, in order to get all of this done back in the early 2000s in order to exonerate vaccines and erase the autism signal?” Grundvig asked.

[…]

Via https://childrenshealthdefense.org/defender/poul-thorsen-former-cdc-scientist-studies-debunk-vaccine-autism-link-plead-guilty/?utm_id=20260830

Four Forms of Numericide

Four Forms of Numericide

By

August 26, 2026

A recent article in the New York Times on the increasing rates of heart disease in young women (Why Are More Young Women Developing Heart Disease?) was amusingly frivolous and about as fact-free as an article about health advice can be.

The key thrust of the article is that any woman who wants to preserve and improve her health should become informed of her “numbers.” Which is to say, she should know her blood pressure, cholesterol, BMI, and hemoglobin A1C (a measure of average blood glucose levels) which are claimed to be “important for assessing risk.”

The Times quotes Dr Priya Freaney, director of the Women’s Heart Care program at Northwestern Medicine: “Knowing your numbers is your most powerful tool,” [she said] “And it’s never too early to start.”

What numbers are we talking about? Well, apparently doctors recommend “all adults strive for these levels:”

  • BP (Blood Pressure) under 120 mm Hg / 80 mm Hg
  • LDL (Low-density lipoprotein) under 100 mg/dL
  • HbA1C (Hemoglobin A1C ) of 5.6 or lower
  • BMI (Body-mass index) under 25

Now the four Horsemen of the Apocalypse, blood pressure, blood sugar, cholesterol, and BMI, threatening to strike you down in your healthy middle age unless you submit to the testing, treating (ie: medications and lifestyle changes), and a retesting paradigm which can lead many to become obsessed by the numbers.

By the way, these four measures have one thing in common: They are typically treated with a prescribing pen that has been carefully guided in your doctor’s expert hands by the helpful people in the pharmaceutical industry. Just saying…

Let’s approach these four with a bit of basic epidemiology, examining the wisdom of telling people of “average risk” to aim for these targets. Obviously, people with pre-existing conditions or those with inherently much higher or multiple risks (such as levels that are in the red flashing light category) involve a different calculus.

But for the sake of evaluating the drive to push people toward these health targets, what do the highest quality studies ultimately say about the value in chasing these numeric targets in healthy people?

Numericide Number One: Blood Pressure at 120/80

I will always remember that old quip from an aging physician: “High blood pressure is better than no blood pressure at all.” But the question one should ask is this: If you lower your blood pressure does it lead to a reduction in your chance of a cardiovascular event or dying?

First off, despite what many guidelines and health care providers say about knowing your numbers, what they should have said was know your cardiovascular risk numbers (your percentage chance of having a heart attack or stroke over the next 10-30 years) not your numbers of cholesterol, blood pressure, or glucose numbers. Those are what we call ‘surrogate markers’ and the only reason to lower these numbers is to possibly reduce your risk of heart attacks and stroke. It’s not that these surrogate numbers are useless — rather they are the wrong numbers to worry about.

[…]

For starters, the target of 120 is not an evidence-based but an “expert-recommended” target, and in case you wondered, having a blood pressure of 130/80 or 140/90 is not the death sentence that your doctor might warn you about. Your blood pressure often jumps all over the map and how and when you measure it can significantly impact that number. It climbs as we get older, naturally. Like grey hair and wrinkles. Chasing this number is one of the biggest uses of a doctor’s time and causes considerable (and frequently unnecessary) worry in patients.

Me? I wish our doctors would have spent time learning more about evidence appraisal and how to properly do shared decision-making with their patients because the decision around the treatment of surrogate numbers is very dependent on a person’s values and preferences.

[…]

The magical “120” comes from the SPRINT trial, a particularly odious piece of work that tortured the data until it showed some benefit of a BP <120 comparted to divergent targets such as <140 in a high-risk population. What most physicians aren’t going to learn is that any apparent benefit evaporated once intensive treatment stopped.

The SPRINT team was behind the 2017 guidelines recommending the 120/80 BP target, but you need to know these guidelines have been discredited for good reason. For instance, the process to produce them was riven with documented conflicts of interest. Again, Big Pharma’s interests are more than well-represented on the guideline production team and their participation automatically broadens the category of people who should take their drug. No — surely that can’t be true? It is true, and to quote a refrain from the movie Airplane, stop calling me Shirley.

The AAFP, American Association of Family Practice— the largest primary care organization in the US — refused to endorse that target. Why? Because, in their words, there were “no significant benefit for all-cause mortality, cardiovascular mortality, myocardial infarction, or renal events.” Let me translate: People don’t live longer or better because you guilt-tripped and drug-equipped them into getting their blood pressure down to 120/80.

There’s also another reason and that has to do with how unsafe it can be to push people’s blood pressure to ridiculously low targets. Not only does this drive people crazy (because many of them have to take two or three or four medications to lower their BP numbers) but it can also lead to falls, fractures, kidney injury, and so on, especially in older adults.

One study in JAMA Internal Medicine found that taking antihypertensive medications was associated with an increased risk of serious fall injuries. SPRINT itself showed nearly double the rate of serious adverse events possibly or definitely related to the antihypertensive drugs.

[…]

Numericide’s Number Two: Low-Density Lipoprotein, or LDL, under 100 mg/dL

This is one of the most aggressively, and irrationally pursued targets: LDL cholesterol. I went back into the data to ask this question: Is there any substantive evidence that an otherwise healthy person with an LDL under 100 mg/dL lives any longer than a person who has an LDL above 100mg/dl?

Basically, should healthy people (what we call ‘primary prevention’) who don’t have a history of a heart attack or heart disease be pushed to get their LDL from, say, 120 to 80 mg/dL? Will this make them live longer?

Sorry to be the bad news bear here, but in a nutshell: No.

The evidence is weak and the absolute benefit is very small. When I mean very small, it’s way smaller than most people expect.

The most comprehensive recent review was published in JAMA in 2022. It was huge, pooling 18 trials of statins for primary prevention including over 85,000 people. The rate of all-cause mortality was statistically significant yet the absolute difference between those who drove their cholesterol that low and those who didn’t was a meagre 0.35%.

The NNT (number needed to treat to prevent one death) was 286.

Another way to say this is that your chance of a normal healthy person dying if they take a statin to drive their LDL below the 100mg/dl target is almost one in 300. Others have strongly contested this number, saying that driving cholesterol down to those levels makes absolutely no difference to the length and quality of a person’s life.

What about older people? You’re in for a surprise here—because in the elderly the situation reverses. A study published in the BMJ in 2016 identified LDL-related studies in the elderly. It found that in a total of over 68,000 elderly people, there was an “inverse association between all-cause mortality and LDL.” Translation: older people with higher LDL levels lived longer! This makes it even more egregious that much of the population taking cholesterol-lowering drugs are over 65 and in the category where they actually need higher cholesterol to stay healthy. 

And then there are the harms of cholesterol lowering drugs, like statins which we know cause muscle weakening, elevated liver enzymes, and diabetes, effects that are consistent across many studies.

Doctors know this from real life experience: most patients (up to 75%) stop taking their statins within 2 years — whether it’s from the adverse effects, the costs or the hassle.

Numericide’s Number Three: HbA1C (Hemoglobin A1C ) of 5.6 or Lower

The crazy low levels at which they tell people to drive their HbA1C down to make me bonkers. What is most nutty is that this nefarious hunt for “prediabetes” which is the granddaddy of all disease-mongering tactics is sold under the logic of ”Why wait until you have full blown diabetes when you can find the ‘pre’ signs early?”

To be clear, the 5.6% is not a treatment target — it’s the “prediabetes diagnostic threshold.” In the ever-reductive world of diabetes “normal” keeps shifting. “Normal” is now considered below 5.7%, prediabetes is 5.7–6.4%, and diabetes is diagnosed at ≥6.5%.

The actual treatment target for most adults with diabetes is <7.0%, a level that sadly labels tens of millions of healthy people as diseased. If you have an HbA1C slightly over 7 and your doctor is pushing a metformin prescription at you, it’s time to push back!

Here’s the core point: the evidence does not support that driving HbA1C to 6.5% or lower extends life. The best available data from two big studies — the ACCORD trial and a meta-analysis from the BMJ — show two very surprising things: either no mortality benefit or actual harm from intensive glucose control.

[…]

Furthermore, there is the opposite thing that could harm you, hypoglycemia — which is often caused by aggressive drug treatment is, in itself, a potent killer.

Just remember that these thresholds are always changed in a uni-directional way, always made lower to expand the pool of patients who allegedly need to be on drugs. This is a process that takes place under the well-documented influence of pharma money, research, and experts, expanding the market for diabetes drugs at each step.

The major push to label people as “prediabetic” — a condition that, incidentally the WHO says shouldn’t be medicalized — is flat-out, brazen disease-mongering.

Having said that, extremely high blood sugar (HbA1C consistently above 9–10%) can cause real harm — kidney failure, blindness, neuropathy, infections. The point isn’t that glucose doesn’t matter at all; it’s that the marginal benefit of pushing from 7.0 to 6.5% or lower does not save lives, and the harm, both in terms of money, medical busy-ness of checking and rechecking your blood sugars, and the harms of the drugs are all real and quantifiable.

Eating a higher quality diet and getting sufficient exercise is the foundation for anyone worried about their blood sugars. Those who are told they have “pre-diabetes” should ignore that advice and refuse to be pasted with a sticky label that causes harm.

Numericide’s Number Four: BMI under 25

Body Mass Index (BMI) is a measure of body weight relative to height, often used to screen whether someone may be underweight, at a healthy weight, overweight, or obese. We need to screen because overweight people live shorter lives, right?

Not necessarily.

We are told that the aim for everyone, concerning this fourth Horseman of the Apocalypse, BMI, is 25. Not only is this absurdly low, but it is essentially meaningless as a measure of health on its own. Anyone with any good musculature whatsoever is going to have a BMI over 25. Why is that? Because muscle weighs more than fat.

It comes down to where the weight sits. A muscular person with BMI of 30 has a different risk profile than a guy with a BMI of 30 who is sedentary with a big beer gut — but the BMI treats them identically.

Where did this “25” come from?

The BMI 25 cutoff comes from a 1995 WHO technical report establishing four categories of body weight (underweight, normal, overweight, obese) and was loosely based on actuarial life insurance data. This threshold was not derived from outcome-based evidence and a BMI of 25 was not linked to any mortality inflection point.

What about someone who has, say, a BMI of 30. Should they get that lower? 

The claim that someone at BMI of 30 has a meaningfully shorter life expectancy than someone at BMI of 25 is not supported by the best available observational evidence.

The largest and most influential meta-analysis on this question was published in JAMA in 2013 and it pooled 97 studies with over 2.88 million participants and more than 270,000 deaths. The findings were mind-blowing: Being overweight was associated with significantly lower all-cause mortality than normal weight.

[…]

Via https://brownstone.org/articles/four-forms-of-numericide/

Why Democrats May Lose the November Elections Even Though Polls Now Say They Can Win

Trump has already rigged the race to crush Democratic voters and ensure a Republican victory—but Democrats don’t want to hear it

The polls confirm a growing surge of voter enthusiasm for Democrats. Are they wrong? No. They may just not be relevant.

While Democrats deliriously high-five themselves at the release of each new favorable poll, Trump has been diligently rigging the electoral process to ensure that Republicans keep control of Congress (and incidentally keep him from being impeached, convicted and thrown in jail for tax evasion and the sexual abuse of minors).

So why may the pro-Democratic poll numbers be irrelevant? Because they only show how people intend to vote, not whether they will actually be able to vote. Or even if they do vote, whether it will make any difference.

Consider these 12 dirty tricks that Trump will use to crush Democratic voters flatter than in the illustration at the outset of this article.

1. Aggressively Partisan Gerrymandering:

Eight state legislatures have already redrawn congressional districts to lock in an artificial Republican House majority even before voting starts. This will dilute millions of Democratic votes across entire states so they will have little or no impact, regardless of overall turnout. Six more states will soon follow their example. And don’t look for the courts to strike down these biased electoral maps: The Supreme Court has already ruled in their favor.

How many House seats will gerrymandering steal for the Republicans in November?

According to redistricting analyses from the Brennan Center for Justice and the Princeton Gerrymandering Project, these new Republican electoral maps now provide a net structural baseline advantage of 14 to 20 House seats for Republicans over a neutral national map.

In a narrowly divided House, where majority rule often hinges on fewer than five seats, gerrymandering alone can determine control of the chamber, regardless of a national lead in the popular vote for Democrats. Having 14 to 20 more seats locked up can make Republican control of the House a slam-dunk, turning the predictive headline of this article into a reality.

2. Announcing “enhanced poll surveillance by ICE to preserve order and prevent illegal voting”:

This will have a chilling effect on Latinos, naturalized citizens, and people of color in general. Many will decide to stay home, because they know that ICE sweeps are fueled by racial profiling, so that even U.S. citizens can disappear into unmarked cars, wind up in detention camps for days or weeks, and even be deported to El Salvador before they are able to prove their citizenship.

Although federal statutes such as 18 U.S.C. § 592, forbid the government from stationing armed federal troops or civil officers at “any place where a general or special election is held,” that will not stop Trump. He will exploit jurisdictional gray areas that permit the staging of immigration or federal enforcement operations outside statutory boundary lines (e.g., 100 to 500 feet away from the polls).

Since many eligible voters live in mixed-status households, with U.S. citizens residing alongside undocumented relatives or green card holders, the threat of immigration sweeps at bus stations and roadways leading to the polls will significantly depress turnout.

Ironically, Trump does not even have to deploy ICE agents at the polls. His mere promise to do so will be enough to trigger the desired chilling effect.

Is there any remedy? Yes. Emergency injunctions can be issued by federal district judges on Election Day under the Ku Klux Klan Act of 1871, which bars conspiracies to intimidate or coerce voters by word or deed. But in the real world, injunctions issued hours into voting will come long after the narrative has already discouraged voter turnout among “suspiciously colored” voters..

[…]

Via https://covertactionmagazine.com/2026/09/11/why-democrats-may-lose-the-november-elections-even-though-polls-now-say-they-can-win/

Pfizer COVID-19 “Vaccine” Plasmid DNA Found Inside Lethal Turbo Cancer of the Heart

We have just completed a new case report that presents one of the most striking findings yet in the debate over COVID-19 “vaccine” turbo cancers: vaccine spike-encoding plasmid DNA was recovered directly from an extremely rare, hyper-aggressive heart tumor.

The McCullough Foundation paper is titled, “Fatal Cardiac Intimal Sarcoma in a 35-Year-Old Male Following COVID-19 mRNA Vaccination: Plasmid DNA Fragments Encoding the S-Protein Detected in Tumor Tissue.”

The patient was a 35-year-old man with no personal or family history of cancer and no identified hereditary cancer predisposition. He received Pfizer-BioNTech BNT162b2 on April 10 and May 4, 2021. Just 170 days after the first dose, doctors discovered a large tumor filling the left atrium of his heart along with multiple brain metastases.

 

Three days later, surgeons removed a 9.0 × 7.0 × 5.3 cm mass from his heart. Pathology confirmed a high-grade cardiac intimal sarcoma, an exceptionally rare and aggressive cancer. Molecular testing found the characteristic abnormalities MDM2 and KDR amplification, while whole-body PET/CT found no other primary tumor elsewhere in the body.

The cancer progressed at an extraordinary pace. Despite open-heart surgery, chemotherapy, radiation, gamma knife treatment, and four brain surgeries, new metastases continued to appear. He ultimately suffered bleeding into a brainstem tumor and died 675 days after diagnosis.

What makes this case especially important is that the growth rate could actually be measured. One brain metastasis grew from about 4 millimeters to 35 millimeters in only 94 days. That works out to a tumor volume doubling time of roughly 10 days.

Then came the most remarkable finding. Archived tissue from the original heart tumor was tested for vaccine components.

PCR detected three separate synthetic, codon-optimized vaccine spike-gene fragments along with the plasmid origin-of-replication sequence. The SV40 enhancer was not detected.

Put simply: vaccine-derived plasmid DNA fragments were found inside the malignant heart tissue itself.

A separate analysis found no intact spike protein and no SARS-CoV-2 nucleocapsid protein in the archived tissue, ruling out infection. One plausible accelerator of this malignancy is the persistence of synthetic vaccine-derived plasmid DNA within the tumor through effects on DNA repair, genomic stability, or tumor-cell proliferation.

This case represents an extremely rare cancer in a young man with no identified conventional cancer predisposition, a massive and already metastatic tumor within 170 days, directly measured explosive growth, and vaccine-derived plasmid DNA recovered from the tumor itself.

These findings directly fit the framework we recently developed in our paper titled, “Potential Oncogenicity of Synthetic mRNA Vaccines: Convergent Mechanistic, Clinical, and Population Evidence for a Concurrent-Hit Model of Accelerated Malignancy.

In that paper, we identified 35 possible oncogenic mechanisms associated with the nucleoside-modified mRNA–lipid nanoparticle platform, converging on four major routes: proto-oncogene activation, increased mutation pressure, disruption of cellular protein networks, and acceleration of cancer stem-cell clones. The model specifically predicts that several of these hits occurring at the same time could compress a cancer process that normally unfolds over years into a much shorter period, particularly in people who already harbor dormant or microscopic disease.

In plain English, the model predicts the kind of pattern seen in the new case report: a hidden cancer clone that may have remained clinically silent can potentially be pushed into rapid growth, immune escape, and metastatic spread when multiple tumor-promoting pressures converge at once.

This cardiac sarcoma case therefore provides important real-world evidence consistent with that model. The patient’s tumor was already enormous and metastatic within months, its measured kinetics indicate extreme acceleration, and vaccine-derived plasmid DNA was recovered directly from the diseased tissue.

For years, turbo cancer has been dismissed as a “myth.” This report, along with the mountain of corroborating evidence, terminates that false claim.

mRNA technology is NOT SAFE FOR HUMAN USE and should be removed from global markets immediately.

[…]

Via https://www.globalresearch.ca/breaking-pfizer-covid-19-vaccine-plasmid-dna-inside-lethal-turbo-cancer-heart/5939892

The 19th century doctors recognized that cancer was caused by vaccines – William Tebb

By Sasha Latypova, 9 September 2026

This is Part 2 of the Cancer Causation series. Part 1 is HERE.

In this post, I am republishing a booklet written in 1892. Mass vaccination, especially of children and women, and laws mandating vaccines had begun in earnest in the mid-1800s. By the end of the century, it was recognised, at least by some doctors, that vaccines induce cancer, which had already begun its unstoppable rise in “civilised” populations, in perfect correlation with increasing “access to modern medicine”. The booklet is as follows.

The Increase of Cancer

(Reprinted from The TOSCIN, of March 12th, 1892.)

By William Tebb, Printed By Wertheimer, Lea & Co., Circus Place, London Wall, I892

SIR,—As the medical journals are reluctant to give currency to suggestions which, throw discredit on certain dogmas of the orthodox medical church, I venture to ask permission, in the interest of the public health, to address your readers on a subject of admitted public importance, the causation of the remarkable and mysterious recrudescence of cancer during the past 30 years. And surely, sir, the study of the sources of any malady, particularly one of so grave and destructive a character, is as well deserving of consideration as the multitudinous but abortive attempts to effect a cure.

I may mention, as an inspiring motive for this communication to the impartial columns of THE TOSCIN, that several of my friends and acquaintances have, after acute and protracted suffering, succumbed to cancer, the origin of which their friends declare to be unaccountable except on the theory below, so that I hardly need an apology for bringing the matter before the attention of those of your readers who are interested in the public health. Cancer, like leprosy, is an incurable disease; and none of the vaunted remedies have stood the test of experience. It can be disseminated like leprosy, and is increasing at an alarming rate. The deaths from cancer in England and Wales are returned by the Registrar-General, thus :— Or per million living.

Cancer is reported to be increasing not only in England and the Continent, but in all parts of the world where vaccination is practised.

Dr. H. McAul Alston, Acting Resident Surgeon, Colonial Hospital, Port of Spain, Trinidad, in the Annual Report to the Surgeon General, dated 5th of April, 1887, says (p. 7):—

Sir James Paget observes:—

It is claimed that cancer is hereditary and is occasionally due to local injury, but is it not obvious that there must be some antecedent constitutional taint or diathesis to give rise to the development of the disease? To what, then, is this condition really due? Sir James Paget also says cancer is due to a morbid condition of the blood, and some of your readers will have little difficulty in pointing out one cause of the morbidity. It is allowed by physicians that cancer may be caused by impregnating the blood with impure matter.

Dr. Joseph Jones, President of the Louisiana Board of Health, a well-known pathologist, says that this disease is inoculable; that cancer may be propagated by inoculation, or by the injection of cancerous matter into the veins. He adds:

Drs. Von Bergman and E. Hahn have demonstrated this by the recent notoriously inhuman experiments at the Berlin Hospital. The Medical Press, December 5th, 1888, quotes Dr. Hahn as:

In The British Medical Journal, June 29th, 1889, Mr. Jonathan Hutchison, F.R.C.S., says that, with due care in the transplantation of a bit of living tissue, cancer may be transferred.

There is probably no method by which inoculation is practised on so large a scale as in vaccination and re-vaccination. It is not now denied by the medical profession that vaccination is an exciting cause of infantile syphilis, and, according to the Registrar-General’s returns, Vaccination Mortality, No. 433, dated 1877, and Infant Mortality, No. 392, dated 1880, the increase in Infantile Syphilis, since vaccination has been compulsory, is fourfold.

Mr. Hibbert, formerly Secretary to the Local Government Board, said in July, 1880, that this terrible increase was one of the most unsatisfactory features of the Vaccination Acts, and a reason why further legislation was needed. Dr. William Forbes Laurie, late medical director of a metropolitan cancer hospital, was thoroughly convinced that the increase of cancer was due to vaccination, and he wrote to Members of Parliament, inviting them to visit the hospital, and witness the terrible result of the vaccine operation. He says this increase of cancer is attributed by some medical men to the large amount of syphilitic disease with which vaccine lymph is impregnated, and by others to the direct impregnation “of healthy persons with lymph imbued with scrofulous and cancerous matter.”

And the late Dr. Dennis Turnbull, who made cancer his particular study for thirty years, declared in the public press his conviction that vaccination and re-vaccination is the most prolific cause of this disease. Mr. Keuchenius, late Colonial Secretary to the Holland Government, called the attention of the Second Chamber to the alarming spread of cancer in the Netherlands, which was coincident with the spread of vaccination, and (as he believed) due to poison conveyed in the vaccine virus.

The British Medical Journal for May 19th, 1885, in a leading article on the increasing fatality of cancer, says:—

Some time ago the Hospital Gazelle reported that fifty infants had been admitted into one hospital suffering from syphilitic disease, and that from some of these infants vaccine lymph had been taken. Assuming that the theory of the British Medical Journal is correct, this is an indication how the cancer spreading virus may be distributed.

In his recent work on cancer (Churchill, 1891), Dr. Herbert Snow calls attention to the fact that cancer is:

The savage it may be noted will not allow his blood to be poisoned with vaccine virus, hence he escapes that morbidity under which cancerous tumours find nutriment. Where the system has become thoroughly infected with this morbid tendency, cure by extirpation or otherwise is admitted to be impossible, and the suffering caused by the apprehension of being the victim of so dreadful an affliction may well engage the attention of your benevolent and thoughtful readers. Dr. Aitken says:

It would, however, be unbecoming in me to dogmatise upon a subject which is admitted to be a puzzle to the medical profession, but I venture to hope that medical practitioners who have had the opportunity which clinical observation affords will no longer keep silence, but in the interests of the public health say whether the suggestion I have ventured to make is borne out by facts within their own experience.

Yours faithfully,

WILLIAM TEBB. Devonshire Club, St. James’, London.vaccine lymph had been taken. Assuming that the theory of the British Medical Journal is correct, this is an indication how the cancer spreading virus may be distributed.

In his recent work on cancer (Churchill, 1891), Dr. Herbert Snow calls attention to the fact that cancer is:

The savage it may be noted will not allow his blood to be poisoned with vaccine virus, hence he escapes that morbidity under which cancerous tumours find nutriment. Where the system has become thoroughly infected with this morbid tendency, cure by extirpation or otherwise is admitted to be impossible, and the suffering caused by the apprehension of being the victim of so dreadful an affliction may well engage the attention of your benevolent and thoughtful readers. Dr. Aitken says:

It would, however, be unbecoming in me to dogmatise upon a subject which is admitted to be a puzzle to the medical profession, but I venture to hope that medical practitioners who have had the opportunity which clinical observation affords will no longer keep silence, but in the interests of the public health say whether the suggestion I have ventured to make is borne out by facts within their own experience.

Yours faithfully,

WILLIAM TEBB. Devonshire Club, St. James’, London.

[…]

Via https://sashalatypova.substack.com/p/vaccines-all-injected-biologics-are