Generational theory, international history and current events
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by tim » Sun Sep 28, 2025 6:08 pm
SW: Elisabet Lann, new Minister of Health, collapses at press conference; ice hockey captain Rasmus Dahlin's fiancée has heart transplant; DE: cyclist Kevin Bonaldo, 25, has cardiac arrest mid-race DE: TV host Troels Mylenberg, 55, beats advanced colon cancer; UKR: diplomat Voskopoja Shkurov has heart attack in Albania; AU: influencer Shinae Ann, 28, has incurable brain cancer; more
Why isn't this the biggest story of them all? COVID "vaccination" has us (barely) living through a GLOBAL POPULATION CRASH The authors of the ongoing democide believe that it will make the world a better place for THEM. We who really want the world to be a better place must stop them, break their power, and indict them.
ABV” stands for “anything but the ‘vaccine.’” We use it to refer to articles whose authors strain to name some other “factors” causing this unprecedented cull.. What better way to preface this apocalyptic overview than to revisit Bill Gates’ (in)famous 2010 Ted Talk, in which he proposed “our” lowering the global population by “10 or 15%,” through “vaccines, health care [sic] and reproductive health services” (i.e., lots more abortions). He cast this project as an urgent one, because “CO2 is warming the planet.”
by tim » Fri Sep 26, 2025 10:25 pm
BREAKING NEWS: My colleague, Edmonton, Alberta Doctor Dr.Darren Markland has DIED SUDDENLY at age 54. Darren was one of my biggest attackers on Twitter.
BREAKING NEWS: My colleague, Edmonton Doctor Dr. Darren Markland has DIED SUDDENLY at age 54. Darren was one of my biggest attackers on X and abused and defamed me for helping cancer patients and for raising concerns about COVID-19 Vaccines and AHS corruption. Darren celebrated when my Cancer Clients were attacked with a fraudulent Court attack on Aug.15 and he hoped that our Ivermectin Cancer Clinic would be permanently closed by Alberta Premier Danielle Smith. “It’s about time”, he said recently, a month before his death. Darren was an ICU doctor who Ventilated and gave Remdesivir to thousands of Albertans during the COVID-19 pandemic. Darren was also one of Alberta’s biggest supporters and promoters of COVID-19 Vaccines. He influenced thousands of Albertans into taking the mRNA jabs. We were complete opposites, yet I was still shocked and very sad to hear about his sudden death. Darren was a cyclist and athlete, he was very physically active. Working in the ICU and being a believer, he would have had every booster and would have taken all 10 recommended COVID-19 Vaccines. The Official story is that he died in a mountain biking accident 2 hours west of Edmonton in a rugged mountainous area. So many times I raised concerns about athletic COVID-19 Vaccinated Canadian doctors dying suddenly while exercising and was attacked and abused mercilessly for it. I stopped tracking Canadian doctor sudden deaths, as no one seemed to care. I wish he had lived to see the error of his ways as a doctor and turned his life around to do good for Albertans. Everyone deserves a second chance to start doing what’s right. Darren and I never met. I wish we had met and talked. We worked a few blocks from each other. I passed by his workplace, Royal Alexandra hospital all the time. We may have gotten along. Rest in peace, Darren. May God grant you mercy.
by tim » Fri Sep 26, 2025 8:44 am
tim wrote: Sun Jan 26, 2025 8:36 am Plague of Corruption: Restoring Faith in the Promise of Science Dr. Judy Mikovits is a modern-day Rosalind Franklin, a brilliant researcher shaking up the old boys’ club of science with her groundbreaking discoveries. And like many women who have trespassed into the world of men, she uncovered decades-old secrets that many would prefer to stay buried. What I Really Think about HIV and Ebola The first concept I want you to understand is called zoonosis, or more properly, zoonotic diseases. If you think it’s a funny word and you immediately imagined a picture of a zoo, you wouldn’t be far off. Zoonosis literally means a disease which can spread between animals and humans. It may surprise you given my reputation as a renegade, but I believe the Centers for Disease Control (CDC) can occasionally provide good, basic information to the public. Here is what they have on their website about zoonotic diseases. Every year, tens of thousands of Americans will get sick from diseases spread between animals and people. These are known as zoonotic diseases. Zoonotic means infectious diseases that are spread between animals and people. Because these diseases cause sickness or death in people, CDC is always tracking them. Animals provide many benefits to people. Many people interact with animals in their daily lives, both at home and away from home. Pets offer companionship and entertainment, with millions of households having one or more pets . . . However, some animals can carry harmful genes that can be shared with people and cause illness—these are known as zoonotic diseases or zoonoses. Zoonotic diseases are caused by harmful germs like viruses, bacteria, parasites, and fungi. These germs can cause many different types of illnesses in people and animals ranging from mild to serious illness to death. Some animals can appear healthy even when they are carrying germs that can make people sick. And the biggest zoonotic disease that is not covered in that list is HIV-AIDS, which affected more than sixty million people leading to our world’s greatest modern plague. While a good deal of ink has been dedicated to the question of how prejudice against the gay lifestyle delayed efforts to properly address the disease, our job as scientists is to provide an explanation of events in the past and how problems might be avoided in the future. Let’s make sure we understand our terms. The human immunodeficiency virus (HIV) is linked to the condition known as acquired immunodeficiency syndrome (AIDS). There was a brief time when the disease was known as gay-related immune disease (GRID), and many activists claim the name change to AIDS prompted a more balanced examination of the disease. Perhaps this is true. But what of the genesis of the retrovirus HIV? Where did it come from? We have a clear answer. It came from a primate. The field agrees the precursor to HIV was the simian immunodeficiency virus or SIV. To be more precise, the human virus came from a monkey or chimpanzee virus. What we were told at the time was that the disease probably jumped to humans as a result of Africans forgetting how to cook their food, in this case chimpanzees, often referred to as “bush meat,” and that the promiscuous sexual lifestyles of African peoples (with implications of possible bestiality with primates) led to the cross-species jump and spread of the virus among the human population. I am now appalled that at the time we did not more closely question these assumptions. Since that time, there have been two competing and, in my mind, closely related theories of how a chimpanzee retrovirus made the jump to humans. The first was popularized by the journalist Edward Hooper and expanded upon in his lengthy 1999 book, The River: A Journey to the Source of HIV and AIDS, for which he conducted more than six hundred interviews. Of the interviews conducted, Hooper was most impressed with evolutionary biologist Bill Hamilton, who, along with other independent researchers such as Louis Pascal, Tom Curtis, and Blaine Elswood, was proposing an idea that, before my work with XMRV, I would have found quite radical. They proposed that the jump from chimpanzees to humans came as a result of vaccine trials in the Belgian Congo from 1957 to 1960 in which more than five hundred common chimpanzees and bonobos (pygmy chimpanzees) were killed so that their kidney cells and sera could be used to grow the oral polio vaccine. This vaccine was subsequently administered to more than a million Africans during that time period. Hooper suggests there was great resistance to this idea, since even in the late 1950s and early 1960s there was little public support for the idea of using chimpanzees in such medical experiments. In addition, the Belgian royal family was publicly supporting the idea of wildlife conservation, and the revelation of these actions would go against that image. Hooper believes another reason for resistance to his idea is that if his theory was accepted, it would shake public confidence in the medical establishment as well as lead to multibillion-dollar class action lawsuits for the AIDS epidemic. This is what Edward Hooper has written on his website about the circumstances surrounding the creation of HIV-AIDS from these experiments and why it makes more sense than the competing bush-meat and “cut hunter” theory. By contrast, the oral polio vaccine (OPV) theory proposes that an experimental OPV that had been locally prepared in chimpanzee cells and administered by mouth, or “fed,” to nearly one million Africans in vaccine trials staged in the then Belgian-ruled territories of the Belgian Congo and Ruanda-Urundi between 1957 and 1960, represents the origin of the AIDS pandemic. It provides a historically-supported background: that between 1956 and 1959 over 500 common chimpanzees (Pan troglodytes schweinfurthi and Pan troglodytes troglodytes) and bonobos or pygmy chimpanzees (Pan paniscus) were housed together at Lindi Camp (Near Stanleyville in the Belgian Congo, or DRC). Hooper goes on to explain that the use of chimpanzees was not technically prohibited by any conventions, but that in most countries around the world at the time, Asian macaques were used in polio virus preparation. As for the claim of other outbreaks, Hooper believes they fit comfortably within the bounds of his theory:</p> <blockquote><a name="calibre_link-251"></a>The OPV theory ascribes the minor outbreaks of AIDS caused by other variants of HIV-1 (Group O, Group N and the more controversial “Group P”) to other polio vaccines (both oral and injected) that were prepared in the cells of chimpanzees and administered in French Equatorial Africa (including Congo Brazzaville and Gabon) in the same late fifties period. It ascribes the outbreak of AIDS from HIV-2 (of which it maintains that only two were epidemic outbreaks) to other polio vaccines (both oral and injected) that were prepared in the cells of sooty mangabeys (or other monkeys that had been caged with sooty mangabeys) and administered in French West Africa in 1956–1960. All the other HIV-2 groups that are claimed by bush-meat theorists have infected just a single person, and some OPV theory supporters argue that dead-end, non-transmissible infections such as these are the natural fate of SIVs that infect human beings via the bushmeat route: that unless they are introduced in an artificial manner (as via a vaccine), they simply die out. I find myself in complete agreement with Hooper’s analysis. Yes, viruses can jump from one species to another, possibly by the eating of an infected animal. But the natural process of degradation by the digestive system, as well as cooking (even when poorly done) is likely to inactivate most pathogens. The second plausible theory, which has come to be known as the “bush-meat” theory, is that sometime early in the twentieth century an individual became infected with SIV from handling chimpanzees or chimpanzee bush-meat. It usually involves the actions of some anonymous native hunter (often called the “cut hunter” because he cut himself shortly after having killed a chimpanzee). Added to this scenario is urbanization encroaching upon the jungle, allowing it to be spread by those newly introduced western evils of prostitution and intravenous drug usage. This theory has recently been expanded by the science writer David Quammen in The Chimp and the River: How AIDS Emerged from an African Forest. Based on an extrapolation of some scientific data, Quammen sets the date for this viral transfer from chimp to human around 1908 in the area known as Leopoldville (later Kinshasa) in the Democratic Republic of the Congo. The description is vivid, and plausible, but I question much about it: Let’s give him due stature: not just a cut hunter but the Cut Hunter. Assuming he lived hereabouts in the first decade of the twentieth century, he probably captured his chimpanzee with a snare made from a forest vine, or in some other form of a trap, and then killed the animal with a spear. He may have been a Baka Pygmy man, living independently with his extended family in the forest or functioning as sort of a serf under the “protection” of a Bantu village chief . . . There’s no way of establishing his identity, nor even his ethnicity, but this remote southeastern corner of what was then Germany’s Kamerun colony offered plenty of candidates . . The chimp too, tethered by a foot or a hand, would have been terrified as the man approached, but also angry and strong and dangerous. Maybe the man killed it without getting hurt; if so, he was lucky. Maybe there was an ugly fight; he might even have been pummeled by the chimp, or badly bitten. But he won. Then he would have butchered his prey, probably on the spot . . . I imagine him opening a long, sudden slice across the back of his left hand, into the muscular web between thumb and forefinger, his flesh smiling out pink and raw almost before he saw the damage or felt it, because his blade was so sharp . . . His blood flowed out and mingled with the chimp’s, the chimp’s flowed in and mingled with his, so that he couldn’t quite tell which was which. He was up to his elbows in gore. He wiped his hand. Blood leaked again into his cut, dribbled again into it from the chimp, and again he wiped. He had no way of knowing, no language or words or thoughts by which to conceive, that this animal was SIV-positive. The idea didn’t exist in 1908. It’s a possible scenario. I can’t say something like that didn’t happen. I just wonder why it hadn’t happened many centuries earlier. Africans had been hunting chimpanzees for thousands of years and cooking them. An interesting addition Quammen makes to the theory is that subsequently the virus spreads slowly among the population. But then starting in 1917, there were vaccination campaigns against sleeping sickness by European doctors who used glass syringes that were reusable. One French colonial doctor during a two-year period treated more than five thousand cases with only six syringes. These campaigns peaked in the early 1950s, and by that time the precursor to the deadly strain of HIV had arisen. When you think about it, you come to the realization there’s a battle of narratives, with science having a definite preference for one over the other. In the first scenario, unwitting scientists release a plague of massive proportions on the population because of their use of questionable animal experiments, infecting more than sixty million people and causing the death of at least thirty-nine million. In the second scenario, a chance event in a jungle encounter with an infected chimpanzee leads to cross-species transmission, then because it’s always a good play to blame urbanization and prostitution, as well as maybe a little inadvertent help from western medicine, and you have a new disease! Is it any surprise that scientists far prefer scenario number two? While I can’t come to a definitive conclusion as to which scenario is more likely, the first one, in which chimpanzees are directly harvested for their organs and the growing of polio virus, makes the most sense to me. It doesn’t have as many moving parts. The virus is in a certain percentage of the five hundred chimpanzees sacrificed. They’re cut up, then used to grow polio vaccine, which is then given orally to nearly a million Africans. And there’s another part of the story that makes Hooper’s account sound more plausible. After Hooper made his claim that the oral polio vaccine grown in chimpanzee tissue and given to humans was the source of the HIV-AIDS epidemic, there was an “investigation.” As I read Hooper’s account, it sounded a lot like the Ian Lipkin investigation into XMRV. In this great investigation, they sampled stocks of polio vaccine from the 1957–1960 period for traces of chimpanzee DNA, or simian virus. Lo and behold, they found NOTHING! There’s just one problem. All of the samples they used were from the United States. They did not have any samples of polio vaccine from Africa. The samples of polio vaccine from the United States had never used chimpanzee tissues as a growth medium or cell line.</p> <p>They DID NOT test African samples of the oral polio vaccine for that which used chimpanzee tissue. This is what Hooper wrote about the supposed investigation into the use of chimpanzee tissue in the development of the polio vaccine that was performed by the Royal Society in September of 2000:</p> Instead of the open and honest debate, and the even-handed investigation of the OPV theory, which had been promised, what actually took place was a carefully-planned attempt to suppress the theory by fair means or foul. The conference became focused around the testing of samples of CHAT vaccine which the parent institute (The Wistar in Philadelphia) had finally released for independent analysis. The vaccinators and the meeting organizers insisted that the vaccine samples were representative of the batches which had been prepared for use in Africa. Since they tested negative for HIV, SIV, and chimpanzee DNA, they concluded that the OPV hypothesis had been disproved— and an acquiescent press largely concurred. The reality, however, was very different. None of the tested samples had ever been near Africa, let alone prepared for the African trials. As the weeks and months passed after the meeting, it became clear that a carefully-organized whitewash was being carried out, partly by the original protagonists (who had, among other things, leant on witnesses to change key parts of their stories), and partly by well-meaning research scientists who could not countenance the possibility that their work of the last ten years might be erroneous, and who secondly were unwilling or unable to imagine that their peers might not be telling the truth. I’ve never met Edward Hooper, but he was writing this in 2004, years before I ever pursued a similar line of inquiry. I’m sure he must have undergone a similar evolution, from hopeful questioner to disillusioned critic. Is it so difficult to imagine that members of an organization will not believe the worst about their own members? Don’t we see the same pattern among police, members of the clergy, and our political class? Isn’t it the rare member of an organization who sees the flaws of their own group?</p> <p>We leave scientists alone in their research and practice, expecting somehow that they can self-police. But we do not even allow the police to self-police. There are citizen review boards, internal affairs, and oversight committees. In a similar manner, we have learned through bitter experience that just because a person is a member of the clergy doesn’t mean they are not capable of crimes against children. We are also beginning to understand that these crimes are not just committed against the flock, but there are more nuns and sisters in the Catholic Church who are coming forward with stories of rape and sexual assault committed by the male members of the clergy. These stories sicken us, but perhaps we have simply trusted too much in unaccountable authorities. Now, maybe Hooper is wrong about his accusation, but it sounds like a pretty serious charge to make. Given what I observed in the “official” investigation into XMRV and the way they cavalierly rewrote basic principles of virology, I’m more inclined to believe Hooper’s account. The scientific establishment tells their stories and expects we will believe them. The simian virus gets transferred into humans, and then the question becomes one of immune activation. What happened in the gay community in the late 1970s and early 1980s? There was a great deal of recreational drug usage, and it’s a scientific fact that anal sex, with its subsequent tearing of tissue, promotes immune activation. The sexual revolution for the heterosexual population, and the lesbian population as well, did not involve such risks. Are dangers to the human population limited to the use of chimpanzee tissue in the development of medical products, or is it a more general question of any animal tissue? I tend to believe the latter and use as an example the controversy over Simian Virus-40 (SV-40) in the same antipolio campaign of the 1950s and 1960s. The concern is that these viruses may lie dormant in people until some form of immune stimulation, just as we saw with HIV and the gay lifestyle that included multiple partners, sexual activity that involved anal tearing, and high recreational drug usage. In her Pulitzer Prize-nominated book, The Pentagon’s Brain, detailing the work of the Defense Advanced Research Projects Agency (DARPA), author Annie Jacobsen provides a brief overview of this controversy. One of the DARPA scientists she interviewed for the book was microbiologist Stephen Block, and this is what she wrote: If the notion of a stealth virus, or silent load, sounded improbable, Block cited a little-known controversy involving the anti-polio vaccination campaign of the late 1950s and early 1960s. According to Block, during this effort millions of Americans risked contracting the “cryptic human infection” of monkey virus, without ever being told. “These vaccines,” writes Block, “were prepared using live African green monkey kidney cells, and batches became contaminated by low levels of a monkey virus, Simian virus 40 (SV 40), which eluded the quality control procedures of the day. As a result, large numbers of people—probably millions in fact—were inadvertently exposed to SV 40.” The controversy over SV 40 was whether it would ultimately lead to cancers in humans decades later. The virus would often be found in cancerous tissues, raising the question of whether it was simply a passenger or a causative agent. Again, this is the same concern raised by the finding of bovine leukemia virus in samples of breast cancer tissue and whether the use of growth hormone in the cattle was prompting the expression of this virus. It’s also worth noting that essentially zero testing is done these days of animal viruses contaminating our vaccines or other medical products. Our medical authorities simply assume we’re all tough enough to fight off these contaminating viruses. Jacobsen continues: Block says that two outcomes of this medical disaster remain debated. One side says the 98 million people vaccinated dodged a bullet. The other side believes there is evidence the vaccine did harm. “A great deal of speculation occurs about whether [simian virus] may be responsible for some diseases” that manifests much later in the vaccinated person’s life, says Block, including cancer. Let’s go to the doubters who agree that at least ninety-eight million people were inoculated with a polio virus that was contaminated with SV-40. Is it reasonable to assume that if you fire ninety-eight million bullets, none will cause any harm? And this only considers the polio vaccine. Every vaccine has been grown in animal tissue, usually of several different species, including monkey, mouse, bird, and cow. Each one of these cross-species events has the potential to transfer a pathogen to humans, or to create some new strain that can cause harm. We have fired several billion bullets of biological ammunition at the human species, and it is the height of arrogance to believe we have caused zero damage. In my discussion of Ebola, I want to highlight an idea many others have been discussing in recent years in one form or another, but that is likely to reconfigure how we go about promoting health.
Dr. Judy Mikovits is a modern-day Rosalind Franklin, a brilliant researcher shaking up the old boys’ club of science with her groundbreaking discoveries. And like many women who have trespassed into the world of men, she uncovered decades-old secrets that many would prefer to stay buried.
What I Really Think about HIV and Ebola The first concept I want you to understand is called zoonosis, or more properly, zoonotic diseases. If you think it’s a funny word and you immediately imagined a picture of a zoo, you wouldn’t be far off. Zoonosis literally means a disease which can spread between animals and humans. It may surprise you given my reputation as a renegade, but I believe the Centers for Disease Control (CDC) can occasionally provide good, basic information to the public. Here is what they have on their website about zoonotic diseases. Every year, tens of thousands of Americans will get sick from diseases spread between animals and people. These are known as zoonotic diseases. Zoonotic means infectious diseases that are spread between animals and people. Because these diseases cause sickness or death in people, CDC is always tracking them. Animals provide many benefits to people. Many people interact with animals in their daily lives, both at home and away from home. Pets offer companionship and entertainment, with millions of households having one or more pets . . . However, some animals can carry harmful genes that can be shared with people and cause illness—these are known as zoonotic diseases or zoonoses. Zoonotic diseases are caused by harmful germs like viruses, bacteria, parasites, and fungi. These germs can cause many different types of illnesses in people and animals ranging from mild to serious illness to death. Some animals can appear healthy even when they are carrying germs that can make people sick. And the biggest zoonotic disease that is not covered in that list is HIV-AIDS, which affected more than sixty million people leading to our world’s greatest modern plague. While a good deal of ink has been dedicated to the question of how prejudice against the gay lifestyle delayed efforts to properly address the disease, our job as scientists is to provide an explanation of events in the past and how problems might be avoided in the future. Let’s make sure we understand our terms. The human immunodeficiency virus (HIV) is linked to the condition known as acquired immunodeficiency syndrome (AIDS). There was a brief time when the disease was known as gay-related immune disease (GRID), and many activists claim the name change to AIDS prompted a more balanced examination of the disease. Perhaps this is true. But what of the genesis of the retrovirus HIV? Where did it come from? We have a clear answer. It came from a primate. The field agrees the precursor to HIV was the simian immunodeficiency virus or SIV. To be more precise, the human virus came from a monkey or chimpanzee virus.
What we were told at the time was that the disease probably jumped to humans as a result of Africans forgetting how to cook their food, in this case chimpanzees, often referred to as “bush meat,” and that the promiscuous sexual lifestyles of African peoples (with implications of possible bestiality with primates) led to the cross-species jump and spread of the virus among the human population. I am now appalled that at the time we did not more closely question these assumptions. Since that time, there have been two competing and, in my mind, closely related theories of how a chimpanzee retrovirus made the jump to humans. The first was popularized by the journalist Edward Hooper and expanded upon in his lengthy 1999 book, The River: A Journey to the Source of HIV and AIDS, for which he conducted more than six hundred interviews. Of the interviews conducted, Hooper was most impressed with evolutionary biologist Bill Hamilton, who, along with other independent researchers such as Louis Pascal, Tom Curtis, and Blaine Elswood, was proposing an idea that, before my work with XMRV, I would have found quite radical. They proposed that the jump from chimpanzees to humans came as a result of vaccine trials in the Belgian Congo from 1957 to 1960 in which more than five hundred common chimpanzees and bonobos (pygmy chimpanzees) were killed so that their kidney cells and sera could be used to grow the oral polio vaccine. This vaccine was subsequently administered to more than a million Africans during that time period. Hooper suggests there was great resistance to this idea, since even in the late 1950s and early 1960s there was little public support for the idea of using chimpanzees in such medical experiments. In addition, the Belgian royal family was publicly supporting the idea of wildlife conservation, and the revelation of these actions would go against that image. Hooper believes another reason for resistance to his idea is that if his theory was accepted, it would shake public confidence in the medical establishment as well as lead to multibillion-dollar class action lawsuits for the AIDS epidemic. This is what Edward Hooper has written on his website about the circumstances surrounding the creation of HIV-AIDS from these experiments and why it makes more sense than the competing bush-meat and “cut hunter” theory. By contrast, the oral polio vaccine (OPV) theory proposes that an experimental OPV that had been locally prepared in chimpanzee cells and administered by mouth, or “fed,” to nearly one million Africans in vaccine trials staged in the then Belgian-ruled territories of the Belgian Congo and Ruanda-Urundi between 1957 and 1960, represents the origin of the AIDS pandemic. It provides a historically-supported background: that between 1956 and 1959 over 500 common chimpanzees (Pan troglodytes schweinfurthi and Pan troglodytes troglodytes) and bonobos or pygmy chimpanzees (Pan paniscus) were housed together at Lindi Camp (Near Stanleyville in the Belgian Congo, or DRC). Hooper goes on to explain that the use of chimpanzees was not technically prohibited by any conventions, but that in most countries around the world at the time, Asian macaques were used in polio virus preparation. As for the claim of other outbreaks, Hooper believes they fit comfortably within the bounds of his theory:</p> <blockquote><a name="calibre_link-251"></a>The OPV theory ascribes the minor outbreaks of AIDS caused by other variants of HIV-1 (Group O, Group N and the more controversial “Group P”) to other polio vaccines (both oral and injected) that were prepared in the cells of chimpanzees and administered in French Equatorial Africa (including Congo Brazzaville and Gabon) in the same late fifties period. It ascribes the outbreak of AIDS from HIV-2 (of which it maintains that only two were epidemic outbreaks) to other polio vaccines (both oral and injected) that were prepared in the cells of sooty mangabeys (or other monkeys that had been caged with sooty mangabeys) and administered in French West Africa in 1956–1960. All the other HIV-2 groups that are claimed by bush-meat theorists have infected just a single person, and some OPV theory supporters argue that dead-end, non-transmissible infections such as these are the natural fate of SIVs that infect human beings via the bushmeat route: that unless they are introduced in an artificial manner (as via a vaccine), they simply die out. I find myself in complete agreement with Hooper’s analysis. Yes, viruses can jump from one species to another, possibly by the eating of an infected animal. But the natural process of degradation by the digestive system, as well as cooking (even when poorly done) is likely to inactivate most pathogens.
The second plausible theory, which has come to be known as the “bush-meat” theory, is that sometime early in the twentieth century an individual became infected with SIV from handling chimpanzees or chimpanzee bush-meat. It usually involves the actions of some anonymous native hunter (often called the “cut hunter” because he cut himself shortly after having killed a chimpanzee). Added to this scenario is urbanization encroaching upon the jungle, allowing it to be spread by those newly introduced western evils of prostitution and intravenous drug usage. This theory has recently been expanded by the science writer David Quammen in The Chimp and the River: How AIDS Emerged from an African Forest. Based on an extrapolation of some scientific data, Quammen sets the date for this viral transfer from chimp to human around 1908 in the area known as Leopoldville (later Kinshasa) in the Democratic Republic of the Congo. The description is vivid, and plausible, but I question much about it: Let’s give him due stature: not just a cut hunter but the Cut Hunter. Assuming he lived hereabouts in the first decade of the twentieth century, he probably captured his chimpanzee with a snare made from a forest vine, or in some other form of a trap, and then killed the animal with a spear. He may have been a Baka Pygmy man, living independently with his extended family in the forest or functioning as sort of a serf under the “protection” of a Bantu village chief . . . There’s no way of establishing his identity, nor even his ethnicity, but this remote southeastern corner of what was then Germany’s Kamerun colony offered plenty of candidates . . The chimp too, tethered by a foot or a hand, would have been terrified as the man approached, but also angry and strong and dangerous. Maybe the man killed it without getting hurt; if so, he was lucky. Maybe there was an ugly fight; he might even have been pummeled by the chimp, or badly bitten. But he won. Then he would have butchered his prey, probably on the spot . . . I imagine him opening a long, sudden slice across the back of his left hand, into the muscular web between thumb and forefinger, his flesh smiling out pink and raw almost before he saw the damage or felt it, because his blade was so sharp . . . His blood flowed out and mingled with the chimp’s, the chimp’s flowed in and mingled with his, so that he couldn’t quite tell which was which. He was up to his elbows in gore. He wiped his hand. Blood leaked again into his cut, dribbled again into it from the chimp, and again he wiped. He had no way of knowing, no language or words or thoughts by which to conceive, that this animal was SIV-positive. The idea didn’t exist in 1908.
It’s a possible scenario. I can’t say something like that didn’t happen. I just wonder why it hadn’t happened many centuries earlier. Africans had been hunting chimpanzees for thousands of years and cooking them. An interesting addition Quammen makes to the theory is that subsequently the virus spreads slowly among the population. But then starting in 1917, there were vaccination campaigns against sleeping sickness by European doctors who used glass syringes that were reusable. One French colonial doctor during a two-year period treated more than five thousand cases with only six syringes. These campaigns peaked in the early 1950s, and by that time the precursor to the deadly strain of HIV had arisen. When you think about it, you come to the realization there’s a battle of narratives, with science having a definite preference for one over the other. In the first scenario, unwitting scientists release a plague of massive proportions on the population because of their use of questionable animal experiments, infecting more than sixty million people and causing the death of at least thirty-nine million. In the second scenario, a chance event in a jungle encounter with an infected chimpanzee leads to cross-species transmission, then because it’s always a good play to blame urbanization and prostitution, as well as maybe a little inadvertent help from western medicine, and you have a new disease! Is it any surprise that scientists far prefer scenario number two? While I can’t come to a definitive conclusion as to which scenario is more likely, the first one, in which chimpanzees are directly harvested for their organs and the growing of polio virus, makes the most sense to me. It doesn’t have as many moving parts. The virus is in a certain percentage of the five hundred chimpanzees sacrificed. They’re cut up, then used to grow polio vaccine, which is then given orally to nearly a million Africans. And there’s another part of the story that makes Hooper’s account sound more plausible. After Hooper made his claim that the oral polio vaccine grown in chimpanzee tissue and given to humans was the source of the HIV-AIDS epidemic, there was an “investigation.” As I read Hooper’s account, it sounded a lot like the Ian Lipkin investigation into XMRV. In this great investigation, they sampled stocks of polio vaccine from the 1957–1960 period for traces of chimpanzee DNA, or simian virus. Lo and behold, they found NOTHING! There’s just one problem. All of the samples they used were from the United States. They did not have any samples of polio vaccine from Africa. The samples of polio vaccine from the United States had never used chimpanzee tissues as a growth medium or cell line.</p> <p>They DID NOT test African samples of the oral polio vaccine for that which used chimpanzee tissue. This is what Hooper wrote about the supposed investigation into the use of chimpanzee tissue in the development of the polio vaccine that was performed by the Royal Society in September of 2000:</p> Instead of the open and honest debate, and the even-handed investigation of the OPV theory, which had been promised, what actually took place was a carefully-planned attempt to suppress the theory by fair means or foul. The conference became focused around the testing of samples of CHAT vaccine which the parent institute (The Wistar in Philadelphia) had finally released for independent analysis. The vaccinators and the meeting organizers insisted that the vaccine samples were representative of the batches which had been prepared for use in Africa. Since they tested negative for HIV, SIV, and chimpanzee DNA, they concluded that the OPV hypothesis had been disproved— and an acquiescent press largely concurred. The reality, however, was very different. None of the tested samples had ever been near Africa, let alone prepared for the African trials.
As the weeks and months passed after the meeting, it became clear that a carefully-organized whitewash was being carried out, partly by the original protagonists (who had, among other things, leant on witnesses to change key parts of their stories), and partly by well-meaning research scientists who could not countenance the possibility that their work of the last ten years might be erroneous, and who secondly were unwilling or unable to imagine that their peers might not be telling the truth. I’ve never met Edward Hooper, but he was writing this in 2004, years before I ever pursued a similar line of inquiry. I’m sure he must have undergone a similar evolution, from hopeful questioner to disillusioned critic. Is it so difficult to imagine that members of an organization will not believe the worst about their own members? Don’t we see the same pattern among police, members of the clergy, and our political class? Isn’t it the rare member of an organization who sees the flaws of their own group?</p> <p>We leave scientists alone in their research and practice, expecting somehow that they can self-police. But we do not even allow the police to self-police. There are citizen review boards, internal affairs, and oversight committees. In a similar manner, we have learned through bitter experience that just because a person is a member of the clergy doesn’t mean they are not capable of crimes against children. We are also beginning to understand that these crimes are not just committed against the flock, but there are more nuns and sisters in the Catholic Church who are coming forward with stories of rape and sexual assault committed by the male members of the clergy. These stories sicken us, but perhaps we have simply trusted too much in unaccountable authorities. Now, maybe Hooper is wrong about his accusation, but it sounds like a pretty serious charge to make. Given what I observed in the “official” investigation into XMRV and the way they cavalierly rewrote basic principles of virology, I’m more inclined to believe Hooper’s account. The scientific establishment tells their stories and expects we will believe them. The simian virus gets transferred into humans, and then the question becomes one of immune activation. What happened in the gay community in the late 1970s and early 1980s? There was a great deal of recreational drug usage, and it’s a scientific fact that anal sex, with its subsequent tearing of tissue, promotes immune activation. The sexual revolution for the heterosexual population, and the lesbian population as well, did not involve such risks. Are dangers to the human population limited to the use of chimpanzee tissue in the development of medical products, or is it a more general question of any animal tissue? I tend to believe the latter and use as an example the controversy over Simian Virus-40 (SV-40) in the same antipolio campaign of the 1950s and 1960s. The concern is that these viruses may lie dormant in people until some form of immune stimulation, just as we saw with HIV and the gay lifestyle that included multiple partners, sexual activity that involved anal tearing, and high recreational drug usage.
In her Pulitzer Prize-nominated book, The Pentagon’s Brain, detailing the work of the Defense Advanced Research Projects Agency (DARPA), author Annie Jacobsen provides a brief overview of this controversy. One of the DARPA scientists she interviewed for the book was microbiologist Stephen Block, and this is what she wrote: If the notion of a stealth virus, or silent load, sounded improbable, Block cited a little-known controversy involving the anti-polio vaccination campaign of the late 1950s and early 1960s. According to Block, during this effort millions of Americans risked contracting the “cryptic human infection” of monkey virus, without ever being told. “These vaccines,” writes Block, “were prepared using live African green monkey kidney cells, and batches became contaminated by low levels of a monkey virus, Simian virus 40 (SV 40), which eluded the quality control procedures of the day. As a result, large numbers of people—probably millions in fact—were inadvertently exposed to SV 40.” The controversy over SV 40 was whether it would ultimately lead to cancers in humans decades later. The virus would often be found in cancerous tissues, raising the question of whether it was simply a passenger or a causative agent. Again, this is the same concern raised by the finding of bovine leukemia virus in samples of breast cancer tissue and whether the use of growth hormone in the cattle was prompting the expression of this virus. It’s also worth noting that essentially zero testing is done these days of animal viruses contaminating our vaccines or other medical products. Our medical authorities simply assume we’re all tough enough to fight off these contaminating viruses. Jacobsen continues: Block says that two outcomes of this medical disaster remain debated. One side says the 98 million people vaccinated dodged a bullet. The other side believes there is evidence the vaccine did harm. “A great deal of speculation occurs about whether [simian virus] may be responsible for some diseases” that manifests much later in the vaccinated person’s life, says Block, including cancer. Let’s go to the doubters who agree that at least ninety-eight million people were inoculated with a polio virus that was contaminated with SV-40. Is it reasonable to assume that if you fire ninety-eight million bullets, none will cause any harm? And this only considers the polio vaccine. Every vaccine has been grown in animal tissue, usually of several different species, including monkey, mouse, bird, and cow. Each one of these cross-species events has the potential to transfer a pathogen to humans, or to create some new strain that can cause harm. We have fired several billion bullets of biological ammunition at the human species, and it is the height of arrogance to believe we have caused zero damage. In my discussion of Ebola, I want to highlight an idea many others have been discussing in recent years in one form or another, but that is likely to reconfigure how we go about promoting health.
The Century of Forgotten Vaccine Hot Lot Disasters How the mantra of "safe and effective" has shielded countless compromised products from scrutiny and led to the same disasters continuously repeating.
One of the greatest challenges with producing a biological pharmaceutical is that it has to be grown in a medium (e.g., a virus within cells or a growth medium for bacteria). This introduces a few major issues. •First, if cell cultures are used, an unrecognized virus may already have infected the cells and contaminated the final product.
by tim » Wed Sep 24, 2025 9:33 am
Large VA COVID vaccine safety study done by Harvard researchers in 2022 shows statistically significant 36% higher risk of heart attack in people who took Pfizer They didn't mention this anywhere in the paper itself. It was buried at the end of the 58 page supplement. I just found out about it when I read the paper.
Press Conference Alert: Eminent German Doctors, Professors, and 200+ Signatories Demand Immediate Ban on mRNA COVID Vaccines Amid Soaring Health Crisis and Plummeting Birth Rates "Today, we are issuing an urgent risk warning and calling for a moratorium on mRNA vaccines, an immediate halt, and an evidence-based reassessment."
California Passes Law Giving State Authority to Set Its Own Vaccine Guidance California Gov. Gavin Newsom last week signed a law granting the state the authority to set its own vaccine guidance based on the recommendations of professional organizations.
by tim » Sun Sep 21, 2025 2:55 pm
FullMoon wrote: Sun Sep 21, 2025 2:06 pm https://substack.com/@naomiwolf/note/c- ... 9?r=4d4v0u Greatest crime against humanity in known history. Spoken by an Jewish MD who's ancestors perished in WW2. Bummer it's true. The deeper question is by whom and for what reason. Because even if the CCP is linked, they had lots of local help. And they're not the only ones doing such heinous things.
U.S. House of Representatives panel yesterday released evidence that a Chinese research team submitted a SARS-CoV-2 genome to a U.S. database on 28 December 2019, nearly 2 weeks before a sequence from another group became public and kick-started the race to develop vaccines and drugs for COVID-19. The revelation, first reported by The Wall Street Journal, renewed allegations that Chinese officials tried to cover up early sequences of the new coronavirus. Lawmakers said the new information also raises the question of whether the U.S. National Institutes of Health’s (NIH’s) GenBank database should somehow flag submissions of pathogen sequences with urgent public health importance. The agency had marked the researcher’s submission as incomplete and deleted the sequence before it became public. The never-completed GenBank submission was “a huge missed opportunity” to start to develop drugs, diagnostics, and vaccines earlier, agrees virologist Jeremy Kamil of Louisiana State University Health Shreveport.
by FullMoon » Sun Sep 21, 2025 2:06 pm
by tim » Sun Sep 21, 2025 9:34 am
Nic Hulscher: Unveiling mRNA’s Impact on Fertility and Health Decoding the science of mRNA’s health crisis
"As birth rates collapse worldwide, finding the key culprits is of the highest importance. Many toxic environmental factors have contributed. However, the great fertility decline was drastically accelerated by mRNA gene-transfer platforms. I joined The Truth Contract podcast to dive deep into this critical, existential issue." - Nicolas Hulscher, MPH
Questions What evidence links mRNA vaccines to declining sperm and egg viability? How has mRNA technology accelerated global fertility challenges since 2020? What broader health risks, beyond reproduction, are emerging from mRNA interventions? Could genomic integration of mRNA be a game-changer in understanding vaccine harms? Are there practical steps individuals can take to mitigate mRNA-related health impacts? Why might batch variability in mRNA vaccines explain differing health outcomes? What does the future hold for humanity if these trends continue unchecked?
by tim » Sun Sep 21, 2025 9:30 am
Patients With Vaccine-Induced Long COVID ‘Don’t Seem to Be Improving’ At a pair of long COVID roundtables Thursday, U.S. Health Secretary Robert F. Kennedy Jr. emphasized the importance of listening to both long COVID patients and the frontline doctors treating them.
“There really is probably a difference between patients with post mRNA injury versus people that have post COVID symptoms,” Redfield said Thursday during a roundtable discussion led by U.S. Health Secretary Robert F. Kennedy Jr. “I will say my post-mRNA injury … patients have a tendency of not improving, they just don’t seem to be improving. I have a number of patients now that are out five years. It’s painful. The COVID infection, patients do have a tendency to improve over time.”
by tim » Sun Sep 21, 2025 9:29 am
CDC Vaccine Advisers May Roll Back Recommendation for Hep B Shot at Birth When it meets today, the CDC’s vaccine advisory committee is expected to revise the current recommendation that all infants be vaccinated against hepatitis B on the day of birth.
‘Alarm Bells’: Genetic ‘Fingerprint’ of COVID Vaccine Found in 31-Year-Old Cancer Patient’s DNA A new preprint study presents the first direct evidence that genetic material from mRNA COVID-19 vaccines can integrate into the human genome, potentially triggering aggressive cancers.
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