Category Archives: Man-made diseases

The Spartacus letter

THE SPARTACUS LETTER

“Damn You To Hell,

You Will Not Destroy America ”

Here Is The ‘Spartacus CO VID Letter’

That’s Gone Viral

There was a deep cover Intel man close to Fauci the whole time. Here is his report.

Disseminate this widely

https://jamesfetzer.org/2021/09/damn-you-to-hell-you-will-not-destroy-america-here-is-the-spartacus-covid-letter-thats-gone-viral/

BY TYLER DURDEN
MONDAY, SEP 27, 2021 – 10:45 AM

Via The Automatic Earth blog,

ZeroHedge Note: This is an anonymously posted document by someone who calls themselves Spartacus. Because it’s anonymous, I can’t contact them to ask for permission to publish. So I hesitated for a while, but it’s simply the best document I’ve seen on Covid, vaccines, etc. Whoever Spartacus is, they have a very elaborate knowledge in “the field”. If you want to know a lot more about the no. 1 issue in the world today, read it. And don’t worry if you don’t understand every single word, neither do I. But I learned a lot.

The original PDF doc is here: Covid19 – The Spartacus Letter
Hello,

My name is Spartacus, and I’ve had enough.
We have been forced to watch America and the Free World spin into inexorable decline due to a biowarfare attack. We, along with countless others, have been victimized and gaslit by propaganda and psychological warfare operations being conducted by an unelected, unaccountable Elite against the American people and our allies.
Our mental and physical health have suffered immensely over the course of the past year and a half. We have felt the sting of isolation, lockdown, masking, quarantines, and other completely nonsensical acts of healthcare theater that have done absolutely nothing to protect the health or wellbeing of the public from the ongoing COVID-19 pandemic.
Now, we are watching the medical establishment inject literal poison into millions of our fellow Americans without so much as a fight.
We have been told that we will be fired and denied our livelihoods if we refuse to vaccinate. This was the last straw.
We have spent thousands of hours analyzing leaked footage from Wuhan, scientific papers from primary sources, as well as the paper trails left by the medical establishment.
What we have discovered would shock anyone to their core.
First, we will summarize our findings, and then, we will explain them in detail. References will be placed at the end.

Summary:

  • COVID-19 is a blood and blood vessel disease. SARS-CoV-2 infects the lining of human blood vessels, causing them to leak into the lungs.
  • Current treatment protocols (e.g. invasive ventilation) are actively harmful to patients, accelerating oxidative stress and causing severe VILI (ventilator-induced lung injuries). The continued use of ventilators in the absence of any proven medical benefit constitutes mass murder.
  • Existing countermeasures are inadequate to slow the spread of what is an aerosolized and potentially wastewater-borne virus, and constitute a form of medical theater.
  • Various non-vaccine interventions have been suppressed by both the media and the medical establishment in favor of vaccines and expensive patented drugs.
  • The authorities have denied the usefulness of natural immunity against COVID-19, despite the fact that natural immunity confers protection against all of the virus’s proteins, and not just one.
  • Vaccines will do more harm than good. The antigen that these vaccines are based on, SARS-CoV- 2 Spike, is a toxic protein. SARS-CoV-2 may have ADE, or antibody-dependent enhancement; current antibodies may not neutralize future strains, but instead help them infect immune cells. Also, vaccinating during a pandemic with a leaky vaccine removes the evolutionary pressure for a virus to become less lethal.
  • There is a vast and appalling criminal conspiracy that directly links both Anthony Fauci and Moderna to the Wuhan Institute of Virology.
  • COVID-19 vaccine researchers are directly linked to scientists involved in brain-computer interface (“neural lace”) tech, one of whom was indicted for taking grant money from China.
  • Independent researchers have discovered mysterious nanoparticles inside the vaccines that are not supposed to be present.
  • The entire pandemic is being used as an excuse for a vast political and economic transformation of Western society that will enrich the already rich and turn the rest of us into serfs and untouchables.

COVID-19 Pathophysiology and Treatments:

COVID-19 is not a viral pneumonia. It is a viral vascular endotheliitis and attacks the lining of blood vessels, particularly the small pulmonary alveolar capillaries, leading to endothelial cell activation and sloughing, coagulopathy, sepsis, pulmonary edema, and ARDS-like symptoms. This is a disease of the blood and blood vessels. The circulatory system. Any pneumonia that it causes is secondary to that.
In severe cases, this leads to sepsis, blood clots, and multiple organ failure, including hypoxic and inflammatory damage to various vital organs, such as the brain, heart, liver, pancreas, kidneys, and intestines.
Some of the most common laboratory findings in COVID-19 are elevated D-dimer, elevated prothrombin time, elevated C-reactive protein, neutrophilia, lymphopenia, hypocalcemia, and hyperferritinemia, essentially matching a profile of coagulopathy and immune system hyperactivation/immune cell exhaustion.
COVID-19 can present as almost anything, due to the wide tropism of SARS-CoV-2 for various tissues in the body’s vital organs. While its most common initial presentation is respiratory illness and flu-like symptoms, it can present as brain inflammation, gastrointestinal disease, or even heart attack or pulmonary embolism.
COVID-19 is more severe in those with specific comorbidities, such as obesity, diabetes, and hypertension. This is because these conditions involve endothelial dysfunction, which renders the circulatory system more susceptible to infection and injury by this particular virus.
The vast majority of COVID-19 cases are mild and do not cause significant disease. In known cases, there is something known as the 80/20 rule, where 80% of cases are mild and 20% are severe or critical. However, this ratio is only correct for known cases, not all infections. The number of actual infections is much, much higher. Consequently, the mortality and morbidity rate is lower. However, COVID-19 spreads very quickly, meaning that there are a significant number of severely-ill and critically-ill patients appearing in a short time frame.
In those who have critical COVID-19-induced sepsis, hypoxia, coagulopathy, and ARDS, the most common treatments are intubation, injected corticosteroids, and blood thinners. This is not the correct treatment for COVID-19. In severe hypoxia, cellular metabolic shifts cause ATP to break down into hypoxanthine, which, upon the reintroduction of oxygen, causes xanthine oxidase to produce tons of highly damaging radicals that attack tissue. This is called ischemia-reperfusion injury, and it’s why the majority of people who go on a ventilator are dying. In the mitochondria, succinate buildup due to sepsis does the same exact thing; when oxygen is reintroduced, it makes superoxide radicals. Make no mistake, intubation will kill people who have COVID-19.
The end-stage of COVID-19 is severe lipid peroxidation, where fats in the body start to “rust” due to damage by oxidative stress. This drives autoimmunity. Oxidized lipids appear as foreign objects to the immune system, which recognizes and forms antibodies against OSEs, or oxidation-specific epitopes. Also, oxidized lipids feed directly into pattern recognition receptors, triggering even more inflammation and summoning even more cells of the innate immune system that release even more destructive enzymes. This is similar to the pathophysiology of Lupus.
COVID-19’s pathology is dominated by extreme oxidative stress and neutrophil respiratory burst, to the point where hemoglobin becomes incapable of carrying oxygen due to heme iron being stripped out of heme by hypochlorous acid. No amount of supplemental oxygen can oxygenate blood that chemically refuses to bind O2.
The breakdown of the pathology is as follows:
SARS-CoV-2 Spike binds to ACE2. Angiotensin Converting Enzyme 2 is an enzyme that is part of the renin-angiotensin-aldosterone system, or RAAS. The RAAS is a hormone control system that moderates fluid volume in the body and in the bloodstream (i.e. osmolarity) by controlling salt retention and excretion. This protein, ACE2, is ubiquitous in every part of the body that interfaces with the circulatory system, particularly in vascular endothelial cells and pericytes, brain astrocytes, renal tubules and podocytes, pancreatic islet cells, bile duct and intestinal epithelial cells, and the seminiferous ducts of the testis, all of which SARS-CoV-2 can infect, not just the lungs.
SARS-CoV-2 infects a cell as follows: SARS-CoV-2 Spike undergoes a conformational change where the S1 trimers flip up and extend, locking onto ACE2 bound to the surface of a cell. TMPRSS2, or transmembrane protease serine 2, comes along and cuts off the heads of the Spike, exposing the S2 stalk-shaped subunit inside. The remainder of the Spike undergoes a conformational change that causes it to unfold like an extension ladder, embedding itself in the cell membrane. Then, it folds back upon itself, pulling the viral membrane and the cell membrane together. The two membranes fuse, with the virus’s proteins migrating out onto the surface of the cell. The SARS-CoV-2 nucleocapsid enters the cell, disgorging its genetic material and beginning the viral replication process, hijacking the cell’s own structures to produce more virus.
SARS-CoV-2 Spike proteins embedded in a cell can actually cause human cells to fuse together, forming syncytia/MGCs (multinuclear giant cells). They also have other pathogenic, harmful effects. SARS-CoV- 2’s viroporins, such as its Envelope protein, act as calcium ion channels, introducing calcium into infected cells. The virus suppresses the natural interferon response, resulting in delayed inflammation. SARS-CoV-2 N protein can also directly activate the NLRP3 inflammasome. Also, it suppresses the Nrf2 antioxidant pathway. The suppression of ACE2 by binding with Spike causes a buildup of bradykinin that would otherwise be broken down by ACE2.
This constant calcium influx into the cells results in (or is accompanied by) noticeable hypocalcemia, or low blood calcium, especially in people with Vitamin D deficiencies and pre-existing endothelial dysfunction. Bradykinin upregulates cAMP, cGMP, COX, and Phospholipase C activity. This results in prostaglandin release and vastly increased intracellular calcium signaling, which promotes highly aggressive ROS release and ATP depletion. NADPH oxidase releases superoxide into the extracellular space. Superoxide radicals react with nitric oxide to form peroxynitrite. Peroxynitrite reacts with the tetrahydrobiopterin cofactor needed by endothelial nitric oxide synthase, destroying it and “uncoupling” the enzymes, causing nitric oxide synthase to synthesize more superoxide instead. This proceeds in a positive feedback loop until nitric oxide bioavailability in the circulatory system is depleted.
Dissolved nitric oxide gas produced constantly by eNOS serves many important functions, but it is also antiviral against SARS-like coronaviruses, preventing the palmitoylation of the viral Spike protein and making it harder for it to bind to host receptors. The loss of NO allows the virus to begin replicating with impunity in the body. Those with endothelial dysfunction (i.e. hypertension, diabetes, obesity, old age, African-American race) have redox equilibrium issues to begin with, giving the virus an advantage.
Due to the extreme cytokine release triggered by these processes, the body summons a great deal of neutrophils and monocyte-derived alveolar macrophages to the lungs. Cells of the innate immune system are the first-line defenders against pathogens. They work by engulfing invaders and trying to attack them with enzymes that produce powerful oxidants, like SOD and MPO. Superoxide dismutase takes superoxide and makes hydrogen peroxide, and myeloperoxidase takes hydrogen peroxide and chlorine ions and makes hypochlorous acid, which is many, many times more reactive than sodium hypochlorite bleach.
Neutrophils have a nasty trick. They can also eject these enzymes into the extracellular space, where they will continuously spit out peroxide and bleach into the bloodstream. This is called neutrophil extracellular trap formation, or, when it becomes pathogenic and counterproductive, NETosis. In severe and critical COVID-19, there is actually rather severe NETosis.
Hypochlorous acid building up in the bloodstream begins to bleach the iron out of heme and compete for O2 binding sites. Red blood cells lose the ability to transport oxygen, causing the sufferer to turn blue in the face. Unliganded iron, hydrogen peroxide, and superoxide in the bloodstream undergo the Haber- Weiss and Fenton reactions, producing extremely reactive hydroxyl radicals that violently strip electrons from surrounding fats and DNA, oxidizing them severely.
This condition is not unknown to medical science. The actual name for all of this is acute sepsis.
We know this is happening in COVID-19 because people who have died of the disease have noticeable ferroptosis signatures in their tissues, as well as various other oxidative stress markers such as nitrotyrosine, 4-HNE, and malondialdehyde.
When you intubate someone with this condition, you are setting off a free radical bomb by supplying the cells with O2. It’s a catch-22, because we need oxygen to make Adenosine Triphosphate (that is, to live), but O2 is also the precursor of all these damaging radicals that lead to lipid peroxidation.
The correct treatment for severe COVID-19 related sepsis is non-invasive ventilation, steroids, and antioxidant infusions. Most of the drugs repurposed for COVID-19 that show any benefit whatsoever in rescuing critically-ill COVID-19 patients are antioxidants. N-acetylcysteine, melatonin, fluvoxamine, budesonide, famotidine, cimetidine, and ranitidine are all antioxidants. Indomethacin prevents iron- driven oxidation of arachidonic acid to isoprostanes. There are powerful antioxidants such as apocynin that have not even been tested on COVID-19 patients yet which could defang neutrophils, prevent lipid peroxidation, restore endothelial health, and restore oxygenation to the tissues.
Scientists who know anything about pulmonary neutrophilia, ARDS, and redox biology have known or surmised much of this since March 2020. In April 2020, Swiss scientists confirmed that COVID-19 was a vascular endotheliitis. By late 2020, experts had already concluded that COVID-19 causes a form of viral sepsis. They also know that sepsis can be effectively treated with antioxidants. None of this information is particularly new, and yet, for the most part, it has not been acted upon. Doctors continue to use damaging intubation techniques with high PEEP settings despite high lung compliance and poor oxygenation, killing an untold number of critically ill patients with medical malpractice.
Because of the way they are constructed, Randomized Control Trials will never show any benefit for any antiviral against COVID-19. Not Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The reason for this is simple; for the patients that they have recruited for these studies, such as Oxford’s ludicrous RECOVERY study, the intervention is too late to have any positive effect.
The clinical course of COVID-19 is such that by the time most people seek medical attention for hypoxia, their viral load has already tapered off to almost nothing. If someone is about 10 days post-exposure and has already been symptomatic for five days, there is hardly any virus left in their bodies, only cellular damage and derangement that has initiated a hyperinflammatory response. It is from this group that the clinical trials for antivirals have recruited, pretty much exclusively.
In these trials, they give antivirals to severely ill patients who have no virus in their bodies, only a delayed hyperinflammatory response, and then absurdly claim that antivirals have no utility in treating or preventing COVID-19. These clinical trials do not recruit people who are pre-symptomatic. They do not test pre-exposure or post-exposure prophylaxis.
This is like using a defibrillator to shock only flatline, and then absurdly claiming that defibrillators have no medical utility whatsoever when the patients refuse to rise from the dead. The intervention is too late. These trials for antivirals show systematic, egregious selection bias. They are providing a treatment that is futile to the specific cohort they are enrolling.
India went against the instructions of the WHO and mandated the prophylactic usage of Ivermectin. They have almost completely eradicated COVID-19. The Indian Bar Association of Mumbai has brought criminal charges against WHO Chief Scientist Dr. Soumya Swaminathan for recommending against the use of Ivermectin.
Ivermectin is not “horse dewormer”. Yes, it is sold in veterinary paste form as a dewormer for animals. It has also been available in pill form for humans for decades, as an antiparasitic drug.
The media have disingenuously claimed that because Ivermectin is an antiparasitic drug, it has no utility as an antivirus. This is incorrect. Ivermectin has utility as an antiviral. It blocks importin, preventing nuclear import, effectively inhibiting viral access to cell nuclei. Many drugs currently on the market have multiple modes of action. Ivermectin is one such drug. It is both antiparasitic and antiviral.
In Bangladesh, Ivermectin costs $1.80 for an entire 5-day course. Remdesivir, which is toxic to the liver, costs $3,120 for a 5-day course of the drug. Billions of dollars of utterly useless Remdesivir were sold to our governments on the taxpayer’s dime, and it ended up being totally useless for treating hyperinflammatory COVID-19. The media has hardly even covered this at all.
The opposition to the use of generic Ivermectin is not based in science. It is purely financially and politically-motivated. An effective non-vaccine intervention would jeopardize the rushed FDA approval of patented vaccines and medicines for which the pharmaceutical industry stands to rake in billions upon billions of dollars in sales on an ongoing basis.
The majority of the public are scientifically illiterate and cannot grasp what any of this even means, thanks to a pathetic educational system that has miseducated them. You would be lucky to find 1 in 100 people who have even the faintest clue what any of this actually means.

COVID-19 Transmission:

COVID-19 is airborne. The WHO carried water for China by claiming that the virus was only droplet- borne. Our own CDC absurdly claimed that it was mostly transmitted by fomite-to-face contact, which, given its rapid spread from Wuhan to the rest of the world, would have been physically impossible.
The ridiculous belief in fomite-to-face being a primary mode of transmission led to the use of surface disinfection protocols that wasted time, energy, productivity, and disinfectant.
The 6-foot guidelines are absolutely useless. The minimum safe distance to protect oneself from an aerosolized virus is to be 15+ feet away from an infected person, no closer. Realistically, no public transit is safe.
Surgical masks do not protect you from aerosols. The virus is too small and the filter media has too large of gaps to filter it out. They may catch respiratory droplets and keep the virus from being expelled by someone who is sick, but they do not filter a cloud of infectious aerosols if someone were to walk into said cloud.
The minimum level of protection against this virus is quite literally a P100 respirator, a PAPR/CAPR, or a 40mm NATO CBRN respirator, ideally paired with a full-body tyvek or tychem suit, gloves, and booties, with all the holes and gaps taped.
Live SARS-CoV-2 may potentially be detected in sewage outflows, and there may be oral-fecal transmission. During the SARS outbreak in 2003, in the Amoy Gardens incident, hundreds of people were infected by aerosolized fecal matter rising from floor drains in their apartments.

COVID-19 Vaccine Dangers:

The vaccines for COVID-19 are not sterilizing and do not prevent infection or transmission. They are “leaky” vaccines. This means they remove the evolutionary pressure on the virus to become less lethal. It also means that the vaccinated are perfect carriers. In other words, those who are vaccinated are a threat to the unvaccinated, not the other way around.
All of the COVID-19 vaccines currently in use have undergone minimal testing, with highly accelerated clinical trials. Though they appear to limit severe illness, the long-term safety profile of these vaccines remains unknown.
Some of these so-called “vaccines” utilize an untested new technology that has never been used in vaccines before. Traditional vaccines use weakened or killed virus to stimulate an immune response. The Moderna and Pfizer-BioNTech vaccines do not. They are purported to consist of an intramuscular shot containing a suspension of lipid nanoparticles filled with messenger RNA. The way they generate an immune response is by fusing with cells in a vaccine recipient’s shoulder, undergoing endocytosis, releasing their mRNA cargo into those cells, and then utilizing the ribosomes in those cells to synthesize modified SARS-CoV-2 Spike proteins in-situ.
These modified Spike proteins then migrate to the surface of the cell, where they are anchored in place by a transmembrane domain. The adaptive immune system detects the non-human viral protein being expressed by these cells, and then forms antibodies against that protein. This is purported to confer protection against the virus, by training the adaptive immune system to recognize and produce antibodies against the Spike on the actual virus. The J&J and AstraZeneca vaccines do something similar, but use an adenovirus vector for genetic material delivery instead of a lipid nanoparticle. These vaccines were produced or validated with the aid of fetal cell lines HEK-293 and PER.C6, which people with certain religious convictions may object strongly to.
SARS-CoV-2 Spike is a highly pathogenic protein on its own. It is impossible to overstate the danger presented by introducing this protein into the human body.
It is claimed by vaccine manufacturers that the vaccine remains in cells in the shoulder, and that SARS- CoV-2 Spike produced and expressed by these cells from the vaccine’s genetic material is harmless and inert, thanks to the insertion of prolines in the Spike sequence to stabilize it in the prefusion conformation, preventing the Spike from becoming active and fusing with other cells. However, a pharmacokinetic study from Japan showed that the lipid nanoparticles and mRNA from the Pfizer vaccine did not stay in the shoulder, and in fact bioaccumulated in many different organs, including the reproductive organs and adrenal glands, meaning that modified Spike is being expressed quite literally all over the place. These lipid nanoparticles may trigger anaphylaxis in an unlucky few, but far more concerning is the unregulated expression of Spike in various somatic cell lines far from the injection site and the unknown consequences of that.
Messenger RNA is normally consumed right after it is produced in the body, being translated into a protein by a ribosome. COVID-19 vaccine mRNA is produced outside the body, long before a ribosome translates it. In the meantime, it could accumulate damage if inadequately preserved. When a ribosome attempts to translate a damaged strand of mRNA, it can become stalled. When this happens, the ribosome becomes useless for translating proteins because it now has a piece of mRNA stuck in it, like a lace card in an old punch card reader. The whole thing has to be cleaned up and new ribosomes synthesized to replace it. In cells with low ribosome turnover, like nerve cells, this can lead to reduced protein synthesis, cytopathic effects, and neuropathies.
Certain proteins, including SARS-CoV-2 Spike, have proteolytic cleavage sites that are basically like little dotted lines that say “cut here”, which attract a living organism’s own proteases (essentially, molecular scissors) to cut them. There is a possibility that S1 may be proteolytically cleaved from S2, causing active S1 to float away into the bloodstream while leaving the S2 “stalk” embedded in the membrane of the cell that expressed the protein.
SARS-CoV-2 Spike has a Superantigenic region (SAg), which may promote extreme inflammation.
Anti-Spike antibodies were found in one study to function as autoantibodies and attack the body’s own cells. Those who have been immunized with COVID-19 vaccines have developed blood clots, myocarditis, Guillain-Barre Syndrome, Bell’s Palsy, and multiple sclerosis flares, indicating that the vaccine promotes autoimmune reactions against healthy tissue.
SARS-CoV-2 Spike does not only bind to ACE2. It was suspected to have regions that bind to basigin, integrins, neuropilin-1, and bacterial lipopolysaccharides as well. SARS-CoV-2 Spike, on its own, can potentially bind any of these things and act as a ligand for them, triggering unspecified and likely highly inflammatory cellular activity.
SARS-CoV-2 Spike contains an unusual PRRA insert that forms a furin cleavage site. Furin is a ubiquitous human protease, making this an ideal property for the Spike to have, giving it a high degree of cell tropism. No wild-type SARS-like coronaviruses related to SARS-CoV-2 possess this feature, making it highly suspicious, and perhaps a sign of human tampering.
SARS-CoV-2 Spike has a prion-like domain that enhances its infectiousness.
The Spike S1 RBD may bind to heparin-binding proteins and promote amyloid aggregation. In humans, this could lead to Parkinson’s, Lewy Body Dementia, premature Alzheimer’s, or various other neurodegenerative diseases. This is very concerning because SARS-CoV-2 S1 is capable of injuring and penetrating the blood-brain barrier and entering the brain. It is also capable of increasing the permeability of the blood-brain barrier to other molecules.
SARS-CoV-2, like other betacoronaviruses, may have Dengue-like ADE, or antibody-dependent enhancement of disease. For those who aren’t aware, some viruses, including betacoronaviruses, have a feature called ADE. There is also something called Original Antigenic Sin, which is the observation that the body prefers to produce antibodies based on previously-encountered strains of a virus over newly- encountered ones.
In ADE, antibodies from a previous infection become non-neutralizing due to mutations in the virus’s proteins. These non-neutralizing antibodies then act as trojan horses, allowing live, active virus to be pulled into macrophages through their Fc receptor pathways, allowing the virus to infect immune cells that it would not have been able to infect before. This has been known to happen with Dengue Fever; when someone gets sick with Dengue, recovers, and then contracts a different strain, they can get very, very ill.
If someone is vaccinated with mRNA based on the Spike from the initial Wuhan strain of SARS-CoV-2, and then they become infected with a future, mutated strain of the virus, they may become severely ill. In other words, it is possible for vaccines to sensitize someone to disease.
There is a precedent for this in recent history. Sanofi’s Dengvaxia vaccine for Dengue failed because it caused immune sensitization in people whose immune systems were Dengue-naive.
In mice immunized against SARS-CoV and challenged with the virus, a close relative of SARS-CoV-2, they developed immune sensitization, Th2 immunopathology, and eosinophil infiltration in their lungs.
We have been told that SARS-CoV-2 mRNA vaccines cannot be integrated into the human genome, because messenger RNA cannot be turned back into DNA. This is false. There are elements in human cells called LINE-1 retrotransposons, which can indeed integrate mRNA into a human genome by endogenous reverse transcription. Because the mRNA used in the vaccines is stabilized, it hangs around in cells longer, increasing the chances for this to happen. If the gene for SARS-CoV-2 Spike is integrated into a portion of the genome that is not silent and actually expresses a protein, it is possible that people who take this vaccine may continuously express SARS-CoV-2 Spike from their somatic cells for the rest of their lives.
By inoculating people with a vaccine that causes their bodies to produce Spike in-situ, they are being inoculated with a pathogenic protein. A toxin that may cause long-term inflammation, heart problems, and a raised risk of cancers. In the long-term, it may also potentially lead to premature neurodegenerative disease.
Absolutely nobody should be compelled to take this vaccine under any circumstances, and in actual fact, the vaccination campaign must be stopped immediately.

COVID-19 Criminal Conspiracy:

The vaccine and the virus were made by the same people.
In 2014, there was a moratorium on SARS gain-of-function research that lasted until 2017. This research was not halted. Instead, it was outsourced, with the federal grants being laundered through NGOs.
Ralph Baric is a virologist and SARS expert at UNC Chapel Hill in North Carolina. This is who Anthony Fauci was referring to when he insisted, before Congress, that if any gain-of-function research was being conducted, it was being conducted in North Carolina.
This was a lie. Anthony Fauci lied before Congress. A felony.
Ralph Baric and Shi Zhengli are colleagues and have co-written papers together. Ralph Baric mentored Shi Zhengli in his gain-of-function manipulation techniques, particularly serial passage, which results in a virus that appears as if it originated naturally. In other words, deniable bioweapons. Serial passage in humanized hACE2 mice may have produced something like SARS-CoV-2.
The funding for the gain-of-function research being conducted at the Wuhan Institute of Virology came from Peter Daszak. Peter Daszak runs an NGO called EcoHealth Alliance. EcoHealth Alliance received millions of dollars in grant money from the National Institutes of Health/National Institute of Allergy and Infectious Diseases (that is, Anthony Fauci), the Defense Threat Reduction Agency (part of the US Department of Defense), and the United States Agency for International Development. NIH/NIAID contributed a few million dollars, and DTRA and USAID each contributed tens of millions of dollars towards this research. Altogether, it was over a hundred million dollars.
EcoHealth Alliance subcontracted these grants to the Wuhan Institute of Virology, a lab in China with a very questionable safety record and poorly trained staff, so that they could conduct gain-of-function research, not in their fancy P4 lab, but in a level-2 lab where technicians wore nothing more sophisticated than perhaps a hairnet, latex gloves, and a surgical mask, instead of the bubble suits used when working with dangerous viruses. Chinese scientists in Wuhan reported being routinely bitten and urinated on by laboratory animals. Why anyone would outsource this dangerous and delicate work to the People’s Republic of China, a country infamous for industrial accidents and massive explosions that have claimed hundreds of lives, is completely beyond me, unless the aim was to start a pandemic on purpose.
In November of 2019, three technicians at the Wuhan Institute of Virology developed symptoms consistent with a flu-like illness. Anthony Fauci, Peter Daszak, and Ralph Baric knew at once what had happened, because back channels exist between this laboratory and our scientists and officials.
December 12th, 2019, Ralph Baric signed a Material Transfer Agreement (essentially, an NDA) to receive Coronavirus mRNA vaccine-related materials co-owned by Moderna and NIH. It wasn’t until a whole month later, on January 11th, 2020, that China allegedly sent us the sequence to what would become known as SARS-CoV-2. Moderna claims, rather absurdly, that they developed a working vaccine from this sequence in under 48 hours.
Stephane Bancel, the current CEO of Moderna, was formerly the CEO of bioMerieux, a French multinational corporation specializing in medical diagnostic tech, founded by one Alain Merieux. Alain Merieux was one of the individuals who was instrumental in the construction of the Wuhan Institute of Virology’s P4 lab.
The sequence given as the closest relative to SARS-CoV-2, RaTG13, is not a real virus. It is a forgery. It was made by entering a gene sequence by hand into a database, to create a cover story for the existence of SARS-CoV-2, which is very likely a gain-of-function chimera produced at the Wuhan Institute of Virology and was either leaked by accident or intentionally released.
The animal reservoir of SARS-CoV-2 has never been found.
This is not a conspiracy “theory”. It is an actual criminal conspiracy, in which people connected to the development of Moderna’s mRNA-1273 are directly connected to the Wuhan Institute of Virology and their gain-of-function research by very few degrees of separation, if any. The paper trail is well- established.
The lab-leak theory has been suppressed because pulling that thread leads one to inevitably conclude that there is enough circumstantial evidence to link Moderna, the NIH, the WIV, and both the vaccine and the virus’s creation together. In a sane country, this would have immediately led to the world’s biggest RICO and mass murder case. Anthony Fauci, Peter Daszak, Ralph Baric, Shi Zhengli, and Stephane Bancel, and their accomplices, would have been indicted and prosecuted to the fullest extent of the law. Instead, billions of our tax dollars were awarded to the perpetrators.
The FBI raided Allure Medical in Shelby Township north of Detroit for billing insurance for “fraudulent COVID-19 cures”. The treatment they were using? Intravenous Vitamin C. An antioxidant. Which, as described above, is an entirely valid treatment for COVID-19-induced sepsis, and indeed, is now part of the MATH+ protocol advanced by Dr. Paul E. Marik.
The FDA banned ranitidine (Zantac) due to supposed NDMA (N-nitrosodimethylamine) contamination. Ranitidine is not only an H2 blocker used as antacid, but also has a powerful antioxidant effect, scavenging hydroxyl radicals. This gives it utility in treating COVID-19.
The FDA also attempted to take N-acetylcysteine, a harmless amino acid supplement and antioxidant, off the shelves, compelling Amazon to remove it from their online storefront.
This leaves us with a chilling question: did the FDA knowingly suppress antioxidants useful for treating COVID-19 sepsis as part of a criminal conspiracy against the American public?
The establishment is cooperating with, and facilitating, the worst criminals in human history, and are actively suppressing non-vaccine treatments and therapies in order to compel us to inject these criminals’ products into our bodies. This is absolutely unacceptable.

COVID-19 Vaccine Development and Links to Transhumanism:

This section deals with some more speculative aspects of the pandemic and the medical and scientific establishment’s reaction to it, as well as the disturbing links between scientists involved in vaccine research and scientists whose work involved merging nanotechnology with living cells.
On June 9th, 2020, Charles Lieber, a Harvard nanotechnology researcher with decades of experience, was indicted by the DOJ for fraud. Charles Lieber received millions of dollars in grant money from the US Department of Defense, specifically the military think tanks DARPA, AFOSR, and ONR, as well as NIH and MITRE. His specialty is the use of silicon nanowires in lieu of patch clamp electrodes to monitor and modulate intracellular activity, something he has been working on at Harvard for the past twenty years. He was claimed to have been working on silicon nanowire batteries in China, but none of his colleagues can recall him ever having worked on battery technology in his life; all of his research deals with bionanotechnology, or the blending of nanotech with living cells.
The indictment was over his collaboration with the Wuhan University of Technology. He had double- dipped, against the terms of his DOD grants, and taken money from the PRC’s Thousand Talents plan, a program which the Chinese government uses to bribe Western scientists into sharing proprietary R&D information that can be exploited by the PLA for strategic advantage.
Charles Lieber’s own papers describe the use of silicon nanowires for brain-computer interfaces, or “neural lace” technology. His papers describe how neurons can endocytose whole silicon nanowires or parts of them, monitoring and even modulating neuronal activity.
Charles Lieber was a colleague of Robert Langer. Together, along with Daniel S. Kohane, they worked on a paper describing artificial tissue scaffolds that could be implanted in a human heart to monitor its activity remotely.
Robert Langer, an MIT alumnus and expert in nanotech drug delivery, is one of the co-founders of Moderna. His net worth is now $5.1 billion USD thanks to Moderna’s mRNA-1273 vaccine sales.
Both Charles Lieber and Robert Langer’s bibliographies describe, essentially, techniques for human enhancement, i.e. transhumanism. Klaus Schwab, the founder of the World Economic Forum and the architect behind the so-called “Great Reset”, has long spoken of the “blending of biology and machinery” in his books.
Since these revelations, it has come to the attention of independent researchers that the COVID-19 vaccines may contain reduced graphene oxide nanoparticles. Japanese researchers have also found unexplained contaminants in COVID-19 vaccines.
Graphene oxide is an anxiolytic. It has been shown to reduce the anxiety of laboratory mice when injected into their brains. Indeed, given SARS-CoV-2 Spike’s propensity to compromise the blood-brain barrier and increase its permeability, it is the perfect protein for preparing brain tissue for extravasation of nanoparticles from the bloodstream and into the brain. Graphene is also highly conductive and, in some circumstances, paramagnetic.
In 2013, under the Obama administration, DARPA launched the BRAIN Initiative; BRAIN is an acronym for Brain Research Through Advancing Innovative Neurotechnologies®. This program involves the development of brain-computer interface technologies for the military, particularly non-invasive, injectable systems that cause minimal damage to brain tissue when removed. Supposedly, this technology would be used for healing wounded soldiers with traumatic brain injuries, the direct brain control of prosthetic limbs, and even new abilities such as controlling drones with one’s mind.
Various methods have been proposed for achieving this, including optogenetics, magnetogenetics, ultrasound, implanted electrodes, and transcranial electromagnetic stimulation. In all instances, the goal is to obtain read or read-write capability over neurons, either by stimulating and probing them, or by rendering them especially sensitive to stimulation and probing.
However, the notion of the widespread use of BCI technology, such as Elon Musk’s Neuralink device, raises many concerns over privacy and personal autonomy. Reading from neurons is problematic enough on its own. Wireless brain-computer interfaces may interact with current or future wireless GSM infrastructure, creating neurological data security concerns. A hacker or other malicious actor may compromise such networks to obtain people’s brain data, and then exploit it for nefarious purposes.
However, a device capable of writing to human neurons, not just reading from them, presents another, even more serious set of ethical concerns. A BCI that is capable of altering the contents of one’s mind for innocuous purposes, such as projecting a heads-up display onto their brain’s visual center or sending audio into one’s auditory cortex, would also theoretically be capable of altering mood and personality, or perhaps even subjugating someone’s very will, rendering them utterly obedient to authority. This technology would be a tyrant’s wet dream. Imagine soldiers who would shoot their own countrymen without hesitation, or helpless serfs who are satisfied to live in literal dog kennels.
BCIs could be used to unscrupulously alter perceptions of basic things such as emotions and values, changing people’s thresholds of satiety, happiness, anger, disgust, and so forth. This is not inconsequential. Someone’s entire regime of behaviors could be altered by a BCI, including such things as suppressing their appetite or desire for virtually anything on Maslow’s Hierarchy of Needs.
Anything is possible when you have direct access to someone’s brain and its contents. Someone who is obese could be made to feel disgust at the sight of food. Someone who is involuntarily celibate could have their libido disabled so they don’t even desire sex to begin with. Someone who is racist could be forced to feel delight over cohabiting with people of other races. Someone who is violent could be forced to be meek and submissive. These things might sound good to you if you are a tyrant, but to normal people, the idea of personal autonomy being overridden to such a degree is appalling.
For the wealthy, neural laces would be an unequaled boon, giving them the opportunity to enhance their intelligence with neuroprosthetics (i.e. an “exocortex”), and to deliver irresistible commands directly into the minds of their BCI-augmented servants, even physically or sexually abusive commands that they would normally refuse.
If the vaccine is a method to surreptitiously introduce an injectable BCI into millions of people without their knowledge or consent, then what we are witnessing is the rise of a tyrannical regime unlike anything ever seen before on the face of this planet, one that fully intends to strip every man, woman, and child of our free will.
Our flaws are what make us human. A utopia arrived at by removing people’s free will is not a utopia at all. It is a monomaniacal nightmare. Furthermore, the people who rule over us are Dark Triad types who cannot be trusted with such power. Imagine being beaten and sexually assaulted by a wealthy and powerful psychopath and being forced to smile and laugh over it because your neural lace gives you no choice but to obey your master.
The Elites are forging ahead with this technology without giving people any room to question the social or ethical ramifications, or to establish regulatory frameworks that ensure that our personal agency and autonomy will not be overridden by these devices. They do this because they secretly dream of a future where they can treat you worse than an animal and you cannot even fight back. If this evil plan is allowed to continue, it will spell the end of humanity as we know it.

Conclusions:

The current pandemic was produced and perpetuated by the establishment, through the use of a virus engineered in a PLA-connected Chinese biowarfare laboratory, with the aid of American taxpayer dollars and French expertise.
This research was conducted under the absolutely ridiculous euphemism of “gain-of-function” research, which is supposedly carried out in order to determine which viruses have the highest potential for zoonotic spillover and preemptively vaccinate or guard against them.
Gain-of-function/gain-of-threat research, a.k.a. “Dual-Use Research of Concern”, or DURC, is bioweapon research by another, friendlier-sounding name, simply to avoid the taboo of calling it what it actually is. It has always been bioweapon research. The people who are conducting this research fully understand that they are taking wild pathogens that are not infectious in humans and making them more infectious, often taking grants from military think tanks encouraging them to do so.
These virologists conducting this type of research are enemies of their fellow man, like pyromaniac firefighters. GOF research has never protected anyone from any pandemic. In fact, it has now started one, meaning its utility for preventing pandemics is actually negative. It should have been banned globally, and the lunatics performing it should have been put in straitjackets long ago.
Either through a leak or an intentional release from the Wuhan Institute of Virology, a deadly SARS strain is now endemic across the globe, after the WHO and CDC and public officials first downplayed the risks, and then intentionally incited a panic and lockdowns that jeopardized people’s health and their livelihoods.
This was then used by the utterly depraved and psychopathic aristocratic class who rule over us as an excuse to coerce people into accepting an injected poison which may be a depopulation agent, a mind control/pacification agent in the form of injectable “smart dust”, or both in one. They believe they can get away with this by weaponizing the social stigma of vaccine refusal. They are incorrect.
Their motives are clear and obvious to anyone who has been paying attention. These megalomaniacs have raided the pension funds of the free world. Wall Street is insolvent and has had an ongoing liquidity crisis since the end of 2019. The aim now is to exert total, full-spectrum physical, mental, and financial control over humanity before we realize just how badly we’ve been extorted by these maniacs.
The pandemic and its response served multiple purposes for the Elite:

  • Concealing a depression brought on by the usurious plunder of our economies conducted by rentier-capitalists and absentee owners who produce absolutely nothing of any value to society whatsoever. Instead of us having a very predictable Occupy Wall Street Part II, the Elites and their stooges got to stand up on television and paint themselves as wise and all-powerful saviors instead of the marauding cabal of despicable land pirates that they are.
  • Destroying small businesses and eroding the middle class.
  • Transferring trillions of dollars of wealth from the American public and into the pockets of billionaires and special interests.
  • Engaging in insider trading, buying stock in biotech companies and shorting brick-and-mortar businesses and travel companies, with the aim of collapsing face-to-face commerce and tourism and replacing it with e-commerce and servitization.
  • Creating a casus belli for war with China, encouraging us to attack them, wasting American lives and treasure and driving us to the brink of nuclear armageddon.
  • Establishing technological and biosecurity frameworks for population control and technocratic- socialist “smart cities” where everyone’s movements are despotically tracked, all in anticipation of widespread automation, joblessness, and food shortages, by using the false guise of a vaccine to compel cooperation.

Any one of these things would constitute a vicious rape of Western society. Taken together, they beggar belief; they are a complete inversion of our most treasured values.
What is the purpose of all of this? One can only speculate as to the perpetrators’ motives, however, we have some theories.
The Elites are trying to pull up the ladder, erase upward mobility for large segments of the population, cull political opponents and other “undesirables”, and put the remainder of humanity on a tight leash, rationing our access to certain goods and services that they have deemed “high-impact”, such as automobile use, tourism, meat consumption, and so on. Naturally, they will continue to have their own luxuries, as part of a strict caste system akin to feudalism.
Why are they doing this? Simple. The Elites are Neo-Malthusians and believe that we are overpopulated and that resource depletion will collapse civilization in a matter of a few short decades. They are not necessarily incorrect in this belief. We are overpopulated, and we are consuming too many resources. However, orchestrating such a gruesome and murderous power grab in response to a looming crisis demonstrates that they have nothing but the utmost contempt for their fellow man.
To those who are participating in this disgusting farce without any understanding of what they are doing, we have one word for you. Stop. You are causing irreparable harm to your country and to your fellow citizens.
To those who may be reading this warning and have full knowledge and understanding of what they are doing and how it will unjustly harm millions of innocent people, we have a few more words.
Damn you to hell. You will not destroy America and the Free World, and you will not have your New World Order. We will make certain of that.
*  *  *
This PDF document contains 14 pages, followed by another 17 pages of references.
For those, please visit the original PDF file at Covid19 – The Spartacus Letter.

Silenced people, David Crowley (murdered)

This is here now…

David Crowley, writer and director of the movie Gray State spoke at the P. A. U. L. Festival at Florida State Fairgrounds in Tampa Friday, August 24th, 2012. David Crowley: Writer and director of the movie Gray State www.indiegogo.com/graystatemovie

From video excerpt:
All I know about this documentary is that the maker and his family were found dead and that supposedly he murdered his family and then killed himself before the movie was released. 5 years later the movie was released but it was about David Crowleys (the original filmmaker ) suicide instead of the original.

This is now happening in front of our very eyes… this man didn’t commit suicide, he and his family was murdered because he wanted to show what is now ahead of us…

David Wilcock on The Great Pandemic: What’s Really Going On?

This is a very good information packet about the current COVID-19 situation, pleas check it out:

Sign up for the entire FREE series of four live masterclasses and see the free 20-minute video here: https://www.ascensionmysteryschool.co… Prepare to dive into the Grand, Unified Conspiracy Theory! 5X more common in Asian males: https://www.biorxiv.org/content/10.11… “Chinese doctors have discovered the coronavirus is designed to attach to lung receptors that are five times more common in Asian males than in African or Indo-European males. Asian females also have less than half the amount of these receptors than Asian males”. Coronavirus is killing 71 to 80 percent men compared to 20 to 29 percent women: https://www.thehour.com/news/article/… Department of Justice Arrests Dr. Charles Lieber and Two Chinese Nationals: https://www.justice.gov/opa/pr/harvar…   Also check this lightning-fast response article from Dr. Michael Salla so you can read more about Defender Europe 20, with links: https://www.exopolitics.org/are-deep-…

AIDS & Ebola, The Man-Made Creation

Always thought this would be the case, but I have never posted anything about it so here we go again… when they just want to destroy us:

AIDS & Ebola, The Man-Made Creation

Why was AIDS originally known as “The Gay Plague” in America? Is AIDS merely a freak accident of nature caused from an African green monkey virus? Or is AIDS a government-sponsored genocide program that seeded a laboratory virus into select populations for political and social purposes?

Is it possible to create pathogenic viruses by genetic engineering? Scientific arguments have been made to support various theories of an artificial origin of AIDS, though these arguments have been suppressed in both the mainstream press and in scientific literature.

The AIDS pandemic started as a direct result of genetic experimentation and military madness. The most damning evidence that AIDS was man-made comes from the Department of Defense (DOD) Appropriations Hearings for 1969 wherein Pentagon officials, namely a one Dr. MacArthur requested an AIDS-like virus, and biowarfare labs dutifully provided a virus which would destroy the human immune response. This genetically-engineered germ would be very different from any previous microbe known to mankind.

Interestingly, the above Hearings on “Synthetic Biological Agents” occurred the same year as the famous Stonewall Riot that won freedom and political clout for the gay community! Neither the government nor the press nor the scientific community has made any effort to bring the above facts to the attention of the public.

Enter the heroic patriots!! There are tireless physicians who have spent years researching and documenting the exhaustive evidence that proves conclusively that HIV/AIDS is in fact biological (germ) warfare experimentation. Whereas both our derelict politicians and mainstream media continue to fail us regarding this most tremendous story of our time! The heroic physicians introduced on this page are the true “saviors” if you will, who alone have exposed the government’s lies and devious smokescreens contrived to conceal an event that is easily the greatest mass murder in world history!! Those who control, manipulate, and censor the major media, are aware of the political and social implications of the AIDS biowarfare story. The reason for AIDS disinformation is obvious: to cover up the man-made origin of this disease. Americans have been duped!!

In his well known report WHO MURDERED AFRICA, Dr. William Campbell Douglass, M.D., wrote that HIV was finally produced (genetically engineered) in 1974, after having been PREDICTED and REQUESTED! He tells us that the AIDS virus by the WHO (World Health Organization), was not just a diabolical scientific exercise that got out of hand. It was a cold-blooded successful attempt to create a killer virus which was then used in a successful experiment in Africa. African AIDS was the result of the smallpox eradication vaccine program conducted by the World Health Organization during the 1970s. It was not an accident. It was deliberate! It is more than hypothetical hyperbole to conclude that our government has conducted biowarfare on Black Africa. It is fact.

For decades depopulation has been the highest long-range priority of US foreign policy towards the Third World. It was classified – it was a secret. “Reduction of the rate of population in these States is a matter of vital US national security.” [ National Security Memorandum, Henry Kissinger ] Viruses cannot jump species unless they are specifically engineered to do so. It is also scientific fact that the AIDS virus bears no resemblance whatsoever to any virus ever found in a green monkey or chimpanzee, but does bear a total resemblance to cow virus and sheep virus, which have been bonded together to create a hybrid virus. The only possible way these two different species of virus could bond together would be from deliberate laboratory manipulation, and then further engineered to make the jump into a human system. HIV is the synthetic biological agent requested by the United States Government to accomplish a hidden Federal program.
The National Institute of Health’s Special Virus Cancer Program (SVCP) is that said hidden Federal program. To attempt to give a comprehensive listing of the old and new documented animal cancer experiments behind the laboratory origin of HIV would fill up this website. Disbelievers and denialists are urged to open their minds. We are dealing here with a worldwide covert genocidal holocaust of unprecedented proportions.

Dr. Robert Strecker is on record saying that science’s new supergerm HIV (this perversion of science), had been worked on being created for 30 to 40 years, and because it was engineered at Ft. Detrick, MD, obviously his claim holds that it was specifically designed as a weapon of mass destruction. As bizarre as it may seem, there are connections between the U.S. Army’s Fort Detrick biowarfare lab and the National Cancer Institute, where Robert Gallo and other leading AIDS researchers worked. (See Emerging Viruses, AIDS and Ebola, by Leonard Horowitz.) The Army’s DEPARTMENT OF BIOLOGICAL WARFARE already has a well-documented tradition of EXPERIMENTATION ON HUMAN BEINGS. And nowhere has homophobia been more blatant or more vicious than in the military. The question arises, why would any homosexual want to serve in the military? Since the beginning of recorded history there has never been a group of people so universally hated and despised as homosexuals. And especially by the Pentagon! What happened in 1978 and beyond to cause AIDS to burst upon the scene and devastate the homosexual segment of the American population?

AIDS in America clearly traces back to the U.S. Federal government’s infamous enterprise of deceit, the hepatitis B experiments performed on thousands of gay volunteers between the years 1978-1981. New York City (in 1083 gay men), San Francisco (in 7000 gay men). The experiment began in Manhattan in November 1978, when over 1,000 homosexuals and bisexuals were injected with the experimental vaccine. Dr. Wolf Szmuness’ experimental hepatitis B vaccine was manufactured by the National Institute of Health (NIH). Also taking part in the study were the Centers for Disease Control (CDC) in Atlanta, the National Institute of Alergy and Infectious Diseases, and big drug companies such as Merck, Sharp & Dohme, and Abbott Laboratories.

To be eligible for the experiment the men had to be young, healthy, promiscuous (emphasis added), and under the age of 40. For statistical purposes — gays were set up — the government tested and interviewed the most promiscuous gays — those signed up in VD clinics for example, and then made the statistics fit the entire gay community. Szmuness had no trouble rounding up gays who were willing to be guinea pigs in a vaccine program that offered health benefits for themselves and their community. Most of the men in the experiment were white. Three months after the experiment began at the New York City Blood Center, the first AIDS case was discovered in a young white Manhattan gay. Beginning in March, 1980, similar vaccine experiments took place in Los Angeles, San Francisco, St. Louis, Denver and Chicago. In the fall of 1980, the first West Coast case of AIDS was reported in a young white gay man from San Francisco.

To this day the New York City Blood Center refuse to release their data on the AIDS deaths following that experiment! The details of the experiment, and its effect on the health of these men, are contained in the records of the trials. However, since 1984, when 64% of the men who got the vaccine already had full-blown AIDS, no additional reports have been released (Waves Forest, “Designer Diseases”, Open Road, Fall 1988, p.3). The U.S. Department of Justice is keeping this incriminating information “classified” and “unavailable” for public research and investigation.

The definitive report of this study can be found in two books by Dr. Alan Cantwell, AIDS and the DOCTORS of DEATH and QUEER BLOOD. Those American gays never realized they were the victims of a secret biomedical plot directed against them. The more one studies the hepatitis B experiment, the more the connections to biological warfare and genocide become apparent. To those perceptive enough to discern it, the mass deaths of homosexuals from AIDS was similar to the mass deaths of Jews in the Holocaust!

With the publication of And The Band Played On in 1987, the media became obsessed with author Randy Shilts’ “Patient Zero” story. A Canadian airline steward named Gaeton Dugas is portrayed as the promiscuous gay man “who brought the AIDS virus from Paris and ignited the epidemic in North America.” What Shilts probably did not know is that when Dugas was diagnosed with AIDS in 1980, over twenty percent of the Manhattan gays in the hepatitis B experiment were HIV positive. This twenty percent infection rate was discovered after the HIV blood test became available in 1985, and after the men’s stored blood at the New York Blood Center was retested for HIV antibodies (JAMA, Vol. 255, pp. 2167-2172, 1986).

Remarkably, these gay men had the highest recorded incidence of HIV anywhere in the world for that time! Even in African populations, where AIDS had been theorized to exist for millennia, there were never reports of such a high incidence of HIV in 1980. The media continue to promote ludicrous propaganda about the origin of AIDS, always avoiding discussion of the idea that HIV came out of a laboratory, and always pointing the finger to Africa.

Dr. Robert B. Strecker, M.D.,Ph.D., was the first AIDS whistleblower, and Lorimar Pictures has bought the screen rights to this most brilliant and courageous doctor’s life story.

Nothing less than a Congressional hearing and investigation that may lead to a full world conference in the United Nations is needed to clarify and defuse the alleged mentally deranged plan of world depopulation through genetically engineered bio-weapons and prevent world panic! Now if silence is complicity, then the American mainstream press IS libel for its continuing, ongoing silence in the face of this diabolic world genocide encompassing the decimation of third world countries for purposes of population control.

The CIA’s want and need for an offensive biological agent to stem the African birth rate is a matter of record documented over 50 years ago. The American people have the right to know and deserve a dialogue on this global genocide of Nuremburg gravity! The massive government cover up and disinformation campaign is expected to escalate (witness the proliferation of certain conspicuous books). Dr. Leonard Horowitz is building a grass roots activist movement to finally expose this great crime against humanity, and to hopefully prevent future bio-attacks against gays and other targeted groups with “ethno-specific” viruses.

The Genome Project makes this technology a very plausible reality for concern. During the late 1950’s, the 60’s, the 70’s, and the early 80’s, scientists and policy makers in the U.S. believed there was a population explosion of peoples who they considered inferior and or undesirable. This is historically the very essence of the intolerant and genocidal mindset. The political consequences for humanity can be disastrous if the new genetic technology is used for evil purposes. The cancer virologists and the genetic engineers are the new masters of life and death on the planet.

Physician/scientist, cancer/AIDS researcher, Dr. Alan R. Cantwell’s AIDS biowarfare books are his classic AIDS AND THE DOCTORS OF DEATH (suppressed at the Fifth International AIDS Conference at Montreal, Canada), and the Benjamin Franklin Award winning sequel, QUEER BLOOD:The Secret AIDS Genocide Plot. 1-800-431-1579. Dr. Cantwell is also author of the revolutionary THE CANCER MICROBE. It is a continuing tragedy that microbiologists, pathologists, oncologists, dermatologists, and other physicians and researchers are not willing to investigate the microbe of cancer. Knowledge of this cancer germ has been suppressed by a greedy and arrogant scientific establishment that does not really want to find a cause and a cure for cancer because it is more lucrative to continue the “search.” Until this infectious agent is recognized, it is doubtful that medical science will ever achieve an effective treatment for AIDS and cancer.

“In the face of a lethal disease, journalists and media editors have been frightened to contradict the conventional wisdom being put across by the scientists. There has been no serious attempt at investigative journalism into the wealth of scientific scandals surrounding AIDS.” – Dr. John Seale.

“We have more evidence on the man-made nature of the AIDS virus than the State of California has on some death-row prisoners,” says Jack Carpenter, the marketing associate of Dr.Robert Strecker and Dr.Alan Cantwell.

Blaming Gays, Blacks, and Chimps for AIDS.

Since the beginning of the AIDS epidemic there have been persistent rumors that the disease was man-made, and that HIV was deliberately “introduced” into the American gay and the African black populations as a germ warfare experiment. This so-called conspiracy theory was quickly squelched by virologists and molecular biolologists, who blamed primates in the African bush and human sexuality for the introduction and spread of HIV.

In the fall of 1986 the Soviets shocked the world by claiming that HIV was secretly developed at Fort Detrick, the U.S. Army’s biological warfare unit. Although the claim was dismissed as “infectious propaganda”, Russian scientists had worked hand in hand with biological warfare scientists in the transfer of viruses and virus-infected tissue into various non-human primates (monkeys, apes, chimps) during the 1970s before AIDS appeared. With improved international relationships, the Russian accusation vanished.

Although evidence supporting the man-made theory has never been mentioned in the major U.S. media, the theory continues to be ridiculed. For example, in the San Francisco Chronicle,( “Quest for the Origin of AIDS”, January 14, 2001), William Carlsen writes: “In the early years of the AIDS epidemic, theories attempting to explain the origin of the disease ranged from the comic to the bizarre: a deadly germ escaped from a secret CIA laboratory; God sent the plague down to punish homosexuals and drug addicts; it came from outer space, riding on the tail of a comet.”

AIDS certainly did not come from the hand of God or outer space. However, there is ample evidence to suspect the hand of man in the outbreak of AIDS that first began in the late 1970s in New York City.

Creating AIDS in animals before the epidemic

Lost in the history of AIDS is evidence pointing to HIV as a virus whose origin traces back to animal cancer retrovirus experimentation in the “pre-AIDS” years of the 1960s and 70s. Evidence linking the introduction of HIV into gays and blacks via vaccine experiments and programs in the late 1970s has been totally ignored in favor of the politically correct theory claiming that HIV originated in chimpanzees in the African rain forest, and that HIV “jumped species” into the African population around 1930 or even earlier.

Conveniently overlooked is the series of outbreaks of AIDS-like epidemics that broke out in U.S. primate centers, beginning in 1969. A decade before AIDS, the first of five recorded epidemics of “simian AIDS” erupted in a colony of stump-tailed macaques housed in a primate lab at Davis, California. Most of the macaques died. Two types of primate immunodeficiency viruses were eventually discovered as the cause. A few silently infected monkeys transferred to the primate colony at Yerkes in Atlanta subsequently died of simian AIDS in the late 1980s. Veterinarians claim the origin of the simian AIDS outbreak is unknown. However, one obvious possibility is the experimental transfer of viruses between various primate species, which is common practice in animal laboratories.

In 1974 veterinarians actually created an AIDS-like disease when newborn chimps were removed from their mothers and weaned exclusively on virus-infected milk from cows infected with “bovine C-type virus.” Within a year the chimps died of leukemia and pneumocystis pneumonia (the “gay pneumonia” of AIDS). Both diseases had never been observed in chimps before this virus-transfer experiment.

Also downplayed is the laboratory creation of feline leukemia and “cat AIDS” by the transfer of HIV-like cat retroviruses in the mid-1970s. These experiments were conducted at Harvard by Myron (Max) Essex, later to become a famous AIDS researcher. All this man-made creation of AIDS in laboratory animals directly preceded the “mysterious” 1979 introduction of HIV into gay men, the most hated minority in America.

Nowadays, scientists hunt for “ancestor” viruses of HIV in chimps in the African wild and ignore all the immunosuppressive viruses that were created in virus laboratories shortly before AIDS. No consideration is given to any of these lab viruses as possible man-made ancestors of the many “strains” of HIV (and HIV-2) that jumped species to produce AIDS in humans.

The gay experiments that preceded AIDS (1978-1981)

Scientists also discount any connection between the official outbreak of AIDS in 1981 and the experimental hepatitis B vaccine program (1978-1981) at the New York Blood Center in Manhattan that used gays as guinea pigs shortly before the epidemic. Curiously, the exact origin of AIDS in the United States remains unstudied. Health authorities simply blame promiscuous gay men, but never adequately explain how a black heterosexual African disease could have transformed itself exclusively into a white young gay male disease in Manhattan.

Researchers claim HIV incubated in Africa for more that a half century until AIDS broke out there in 1982. However, in the U.S. there was no incubation period for gay men. As soon as homosexuals signed up as guinea pigs for government-sponsored hepatitis B vaccine experiments, they began to die with a strange virus of unknown origin. The hepatitis B experiments began in Manhattan in the fall of 1978; the first few cases of AIDS (all young gays from Manhattan) were reported to the CDC in 1979.

Scientists have also failed to explain how a brand new herpes virus was also introduced exclusively into gays, along with HIV, in the late 1970s. This herpes virus is now believed to be the cause of Kaposi’s sarcoma, the so-called “gay cancer” of AIDS. Before AIDS, Kaposi’s sarcoma was never seen in healthy young men. Identified a decade after HIV, in 1994, this KS virus is closely related to a primate cancer-causing herpes virus extensively studied and transferred in animal laboratories in the decade before AIDS.

Also downplayed to the public is a new microbe (Mycoplasma penetrans), also of unknown origin, that was introduced into homosexuals, along with HIV and the new herpes virus. Thus, not one but three new infectious agents were inexplicably transferred into the gay population at the start of the epidemic (HIV, the herpes KS virus, and M.penetrans).

In his book, Virus [2000], Luc Montagnier (the French virologist who co-discovered HIV) blames promiscuous American gay tourists for bringing this new mycoplasma to Africa, and for bringing back HIV. He provides no evidence for this homophobic theory. Nor does he mention the various mycoplasmas that were passed around in the 1970s in scientific labs, and the fact that these microbes were frequent contaminants in virus cultures and vaccines.

Why are all these simultaneous introductions of new infectious agents into gay men ignored by scientists? Surely a credible explanation would be important in determining the origin of HIV and AIDS.

Why are scientists so opposed to the man-made theory? And why do they believe so passionately in the chimp theory? One explanation might be that scientists don’t want the public to know what happened to the tens of thousands of imported primates who were held captive in laboratories throughout the world in the decade before AIDS.

The forgotten Special Virus Cancer Program (1964-1977)

Rarely mentioned by AIDS scientists and media reporters is the fact that surgeons have been transplanting chimpanzee parts (and chimp viruses) into people for decades. When Keith Reemtsma died in June 2000, at age 74, he was hailed as a pioneer in cross-species organ transplants (now known as xenotransplantation). By 1964 he had already placed six chimpanzee kidneys into six patients. All his patients died, but eventually Reemtsma succeeded in many successful human-to-human organ transplants.

Much more likely to have spread primate (chimp and monkey) viruses to human beings is the largely forgotten Special Virus Cancer Program (SVCP). This research program was responsible for the development, the production, the seeding, and the deployment of various animal cancer and immunosuppressive AIDS-like viruses and retroviruses. These laboratory created viruses were capable of inducing disease when transferred between animal species and also when transplanted into human cells and tissue.

The SVCP began in 1964 as a government-funded program of the National Cancer Institute (NCI) in Bethesda, Maryland. Originally designed to study leukemia, the program was soon enlarged to study all forms of cancer. The scope of the program was international and included scientists from Japan, Sweden, Italy, the Netherlands, Israel, and Africa. The mission of the SVCP was to collect various human and animal cancers from around the world and to grow large amounts of cancer-causing viruses. As a result, thousands of liters of dangerous man-made viruses were adapted to human cells and shipped around the world to various laboratories. The annual reports of the SVCP contain proof that species jumping of animal viruses was a common occurrence in labs a decade before AIDS.

The SVCP gathered together the nation’s top virologists, biochemists, immunologists, molecular biologists, and epidemiologists, to determine the role of viruses and retroviruses in the production of human cancer. Many of the most prestigious medical institutions were involved in this program. Connected with the SVCP were the most famous future American AIDS scientists, such as Robert Gallo (the co-discoverer of HIV), Max Essex of “cat AIDS” fame, and Peter Duesberg, who claims HIV does not cause AIDS. Gallo and Essex were also the first to promote the widely accepted African green monkey theory of AIDS. This theory was proven erroneous as far back as 1988, but was heavily circulated among AIDS educators and the media until the theory was superceded by the chimp theory in the late 1990s.

Biowarfare research, primate research and the SVCP

Also joining forces with the SVCP at the NCI were the military’s biological warfare researchers. On October 18, 1971, President Richard Nixon announced that the army’s biowarfare laboratories at nearby Fort Detrick, Maryland, would be converted to cancer research. As part of Nixon’s so-called War on Cancer, the military biowarfare unit was retitled the new Frederick Cancer Research Center, and Litton Bionetics was named as the military’s prime contractor for this project.

According to the 1971 SVPC annual report, the primary task of the now jointly connected National Cancer Institute-Frederick Cancer Research Center was “the large scale production of oncogenic (cancer-causing) and suspected oncogenic viruses to meet research needs on a continuing basis.” Special attention was given to primate viruses (the alleged African source of HIV) and “the successful propagation of significant amounts of human candidate viruses.” Candidate viruses were animal or human viruses that might cause human cancers.

For these experiments a steady supply of research animals (monkeys, chimpanzees, mice, and cats) was necessary; and multiple breeding colonies were established for the SVCP. Primates were shipped in from West Africa and Asia for experimentation; and virus-infected animals were shipped out to various labs worldwide.

By 1971, a total of 2,274 primates had been inoculated at Bionetics Research Laboratories, under contract to Fort Detrick. Over 1000 of these monkeys had already died or had been transferred to other primate centers. (Some animals were eventually released back into the wild). By the early 1970s, experimenters had transferred cancer-causing viruses into several species of monkeys, and had also isolated a monkey virus (Herpesvirus saimiri) that would have a close genetic relationship to the new Kaposi’s sarcoma herpes virus that produced the “gay cancer” of AIDS in 1979.

In order to induce primates and other research animals to acquire cancer, their immune system was deliberately suppressed by drugs, radiation, or cancer-causing chemicals or substances. The thymus gland and/or the spleen were removed, and viruses were injected into newborn animals or into the womb of pregnant animals. Some animals were injected with malaria to keep them chronically sick and immunodepressed.

The U.S. is the world’s leading consumer of primates, and 55,000 are used yearly in medical research. Primates (especially newborn and baby chimpanzees) are the most favored lab animals because they are similar biochemically and immunologically to human beings. Humans share 98.4% of their DNA with chimpanzees. Chimps were extensively used by SVCP because there would be no official testing of “candidate” lab viruses on humans.

In the decade before AIDS, Gallo was a project officer of a primate study contracted by Bionetics that pumped cancerous human tissue, as well as a variety of chicken and monkey viruses, into newborn macaques (a small species of monkey that carries a close relative of the KS virus). Recorded in the 1971 SVCP report (NIH-71-2025), Gallo’s project notes state: “Inasmuch as tests for the biological activity of candidate human viruses will not be tested in the human species, it is imperative that another system be developed for these determinations, and subsequently for the evaluation of vaccines or other measures of control. The close phylogenetic relationship of the lower primates to man justifies utilization of these animals for these purposes.”

Researchers at Bionetics injected human and animal cancer material into various species of monkeys to determine the cancer effect. Newborn and irradiated monkeys were injected with blood (“using multiple sites and volumes as large as possible”) taken from various forms of human leukemia. In other studies, tissue cultures infected with various animal viruses were inoculated into primates. How many “new” and “emerging” viruses were created and adapted to human tissue and to various primates is not known. Some primates were released back into the wild carrying lab viruses with them. The possible spread of these lab viruses to other animals in the wild has been ignored by scientists searching for the origin of HIV and its close relatives in African animals.

Cats were also bred for leukemia and sarcoma cancer studies. Germ free colonies of inbred mice were established. Mouse cancer viruses were manipulated to produce resistant and non-resistant strains. These adapted viruses would be employed in the 1980s in human gene replacement experiments. Such experiments utilized a weakened strain of the mouse leukemia virus to infect and “taxi-in” the missing genes to genetically-defective human beings.

The end of the SVCP and the birth of AIDS

By 1977 the SVCP came to an inglorious end. According to Gallo, “Scientifically, the problem was that no one could supply clear evidence of any kind of human tumor virus, not even a DNA virus, and most researchers refused to concede that viruses played any role in human cancers. Politically, the Virus Cancer Program was vulnerable because it attracted a great deal of money and attention and had failed to produce dramatic, visible results.”

Despite all this, the SVCP was the birthplace of genetic engineering, molecular biology, and the human genome project. More than any other program it built up the field of animal retrovirology, which led to the vital understanding of cancer and immunosuppressive retroviruses in humans. As the SVCP was winding down, thousands of gay men were signing up as guinea pigs in government-sponsored hepatitis B vaccine experiments in New York, Los Angeles, and San Francisco. These same cities would soon become the three primary epicenters for the new “gay-related immune deficiency syndrome,” later known as AIDS.

Two years after the termination of the SCVP, the introduction of HIV into gay men (along with a herpes virus and a mycoplasma) miraculously revived retroviral research and made Gallo the most famous scientist in the world. Could virus-contaminated hepatitis vaccines lie at the root of AIDS? In the early 1970s the hepatitis B vaccine was developed in chimpanzees. To this day, some people are fearful about taking the hepatitis B vaccine because of its original connection to gay men and AIDS. Was HIV (and the KS herpes virus and a new mycoplasma) introduced into gays during these vaccine trials when thousands of homosexuals were injected in Manhattan beginning in 1978, and in the West Coast cities in 1980-1981?

As mentioned, the first gay AIDS cases erupted in Manhattan a few months after the gay experiment began at the NY Blood Center. When a blood test for HIV became available in the mid-1980s, the Center’s stored gay blood specimens were reexamined. Most astonishing is the statistically significant fact that 20% of the gay men who volunteered for the hepatitis B experiment in New York were discovered to be HIV-positive in 1980 (a year before the AIDS epidemic became “official” in 1981). This signifies that Manhattan gays in 1980 had the highest incidence of HIV anywhere in the world, including Africa, the supposed birthplace of HIV and AIDS. And epidemic cases in Africa did not appear until 1982.

Although denied by the AIDS establishment, a few researchers are convinced that these vaccine experiments served as the vehicle through which HIV was introduced into the gay population. My own extensive research into the hepatitis B experiments is presented in AIDS and the Doctors of Death: An Inquiry into the Origin of the AIDS Epidemic [1988], and in Queer Blood: The Secret AIDS Genocide Plot [1993]. These books also debunk the preposterous “Patient Zero” story of 1987, which claimed a promiscuous gay Canadian airline steward brought AIDS to America. The highly implausible story was sensationalized in the media and served to further obscure the origin of AIDS in America and blame gay promiscuity.

Even Montagnier is doubtful that the U.S. epidemic could have developed from a single patient. Never mentioned by proponents of the chimp theory is the fact that the New York Blood Center established a chimp virus laboratory in West Africa in 1974. One of the purposes of VILAB II, at the Liberian Institute for Biomedical Research in Robertsfield, Liberia, was to develop the hepatitis B vaccine in chimps. A few years later this vaccine was inoculated into gays at the Center.

Chimps were captured from various parts of West Africa and brought to VILAB. Alfred Prince, Head of virology at the NY Blood Center, has been the director of Vilab for the past 25 years. The lab prides itself by releasing “reha bilitated” chimps back into the wild.

Also closely allied with “pre-AIDS” development of a hepatitis B vaccine is the little publicized primate colony outside New York City called LEMSIP (the Laboratory for Experimental Medicine and Surgery). Until disbanded in 1997, LEMSIP supplied New York area scientists with primates and primate parts for transplantation and virus research.

Founded in 1965, LEMSIP was affiliated with the New York University Medical Center, where the first cases of AIDS-associated Kaposi’s sarcoma were discovered in 1979. Researchers at NYU Medical Center were also heavily involved in the development of the experimental hepatitis B vaccine used in gays; and the Medical Center received government grants and contracts connected with biological warfare research beginning in 1969, according to Leonard Horowitz, author of Emerging Viruses: AIDS and Ebola [1996].

Scientific disinformation and the 1959 HIV-positive blood test from Africa

By predating HIV back to the 1930s, the chimp theory effectively discredits the man-made theory of AIDS, which dates the introduction of HIV to the late 1970s. Only time will tell whether the chimp theory will hold up to further scientific scrutiny.

Conspiracy theorists believe some wildly popular AIDS origin stories in the press reek of scientific disinformation. One example is the Patient Zero story. Another is the media blitz surrounding the English sailor who supposedly contracted AIDS in 1959. This now-disproven story made worldwide headlines in 1990 and obviously served to contradict the underground conspiracy theory (particularly among African-Americans) that AIDS was man-made.

The New York Times (July 24, 1990) declared: “The case also refutes the widely publicized charges made by Soviet officials several years ago that AIDS arose from a virus that had escaped from a laboratory experiment that went awry or was a biological warfare agent. The human retrovirus group to which the AIDS virus belongs was unknown at the time. Nor did scientists then have the genetic engineering techniques needed to create a virus.” Several years later, the case was discovered to be not a case of AIDS because the sailor’s tissue remains were accidentally (or deliberately) contaminated with HIV.

In 1998 the media alerted the public to further evidence that AIDS started in Africa. The proof consisted of an old 1959 stored frozen blood specimen discovered to be HIV-positive. Researchers claimed the tiny amount of serum contained fragments of HIV “closely related” to a virus found in 3 chimpanzees in the African wild and in the frozen remains of a chimp named Marilyn, discovered in a freezer at Fort Detrick.

The 1959 specimen was obtained from a Bantu man living in Kinshasa, the Congo. His name and health status were not recorded. Details of the history and testing of this specimen (later heralded as the “world’s oldest HIV-positive blood sample”) are recorded in The River: A Journey to the Source of HIV and AIDS [1999], by journalist Edward Hooper who theorizes that HIV was introduced into Africans via the polio vaccine programs in the late 1950s. Hooper claims the polio vaccine was prepared using chimp kidney cells contaminated with the ancestor virus of HIV.

When tested for HIV in the mid-1980s, the 1959 blood sample was the only specimen out of 700 stored frozen Congo bloods that tested positive for HIV. Originally collected by Arno Motulsky on a Rockefeller grant, the African sample was one of many sent to the University of Washington in Seattle and used for genetic testing and included in a report, “Population Genetic Studies,” published in 1966. Around 1970, the remaining 672 frozen bloods were flown to Emory University in Atlanta for further genetic tests.

In 1985 the specimens again changed hands, this time for HIV testing by Andre Nahmias, a virologist and animal researcher associated with the Yerkes Primate Center at Emory. The Congo specimens were tested along with 500 other blood specimens taken from blacks living in sub-Saharan Africa between the years 1959 and 1982. Initially over 90% of specimens taken in 1959 tested positive for HIV by the ELISA test. However, these HIV-positive tests were later determined to be false-positive. After the examinations at Emory, the specimens were shipped to Harvard University in Cambridge, Massachusetts, for HIV testing in Max Essex’ lab.

Three specimens initially tested HIV-positive, but finally only the 1959 specimen from the unidentified Bantu man was confirmed HIV- positive. Around the time of these examinations, Essex’s lab was unknowingly contaminated with primate viruses.

In 1986, Essex discovered a new “human” AIDS virus that later proved to be a contaminating monkey virus. The source of the primate virus traced back to a captive monkey at a primate center in nearby Southborough, Massachusetts. This primate contamination at his lab resulted in the erroneous green monkey theory, heavily popularized by Gallo and the media.

Also unpublicized is the little known fact that Gallo’s lab at the National Cancer Institute was plagued with contamination by primate viruses. In 1975 he reported a new human “HL-23” virus that eventually proved to be three contaminating ape primate viruses (gibbon-ape virus, simian sarcoma virus, and baboon endogenous virus). Gallo claims he has no idea how these viruses contaminated his research.

In 1996 Hooper convinced Nahmias to turn over the remaining 1959 specimen to David Ho of Rockefeller University in Manhattan for PCR testing. In 1996 Ho was named Time magazine’s “Man of the Year”, at a time when few people had ever heard of him. Ho is also the director of the Aaron Diamond AIDS Research Center, affiliated with Rockefeller University since 1996. The Diamond Center is also now connected with the New York Blood Center, home of the gay vaccine experiments that gave birth to AIDS.

Ho determined the tiny amount of the remaining specimen did not contain live virus, nor was the complete virion of the virus present. Instead, some fragments of the virus (about 15% of the total genome) were tested and presented to the scientific world as the oldest specimen of HIV in the world. Ho’s PCR results cannot be confirmed by independent investigators because the 1959 specimen is now totally used up.

When published in the journal Nature on February 5, 1998 (“An African HIV-1 sequence from 1959 and implications for the origin of the epidemic”), Hooper’s name appeared on the report, along with Ho, Bette Korber, Nahmias, and others, The report was heavily publicized as proof that HIV existed in the African population in 1959.

Although there are no HIV-positive tissue specimens from Africa from the 1960s and 1970s, and no proven cases of AIDS either, Hooper relies heavily on this 1959 test to support his theory that HIV entered the African population via the polio vaccines programs in the late 1950s.

In The River Hooper quickly dismisses the claims of physician Robert Strecker, the first whistle-blower of man-made AIDS, as well as the research in Horowitz’s Emerging Viruses, and in my own books, AIDS & The Doctors of Death, and Queer Blood.

In condemning AIDS biowarfare research, Hooper declares, “Sadly, supporters of the Streckers have continued to peddle their ill-informed and outdated versions of the myth, blaming variously the Soviets, the CIA, the Germans, and the World Health Organization (WHO) well into the nineties.” He dismisses the hepatitis B vaccine connection to AIDS by noting that only two of the 826 gay vaccinees had developed AIDS by 1983. Hooper ignores the fact that by 1981 over 20% of the men in the trials were HIV-positive and that by 1982, over 30% of the men were HIV-positive. He dismisses the World Health Organization’s African smallpox vaccine connection by saying, “there is no reason for either HIV or SIV [simian immunodeficiency virus] to be accidentally present in the vaccine.” Hooper fails to consider the possibility that the vaccines could have been deliberately contaminated with HIV. Hooper has been a United Nations official, but no details of this are included in his book .

Despite his massive research, Hooper seems naïve about the continuing transfer of viruses between various primate species at primate centers. For example, in 1995 he interviewed Preston Marx at LEMSIP. At that time Marx was a representative of David Ho’s organization, the Aaron Diamond Research Center. Hooper writes: “I was shocked by the cavalier way in which tissues and sera from one species had been introduced into other species, long after the risks of cross-species transfer had been highlighted by the SV40 [polio vaccine] debacle, and I was astonished that survivors from troops that had been stricken by mystery illnesses could have been casually sold to other centers, for use in experiments there. Furthermore, this apparent lack of monitoring and central control seemed to be echoed in other fields, like xenotransplantation (the transplanting of organ or cells from one species to another) — and here, of course, the implications were even more frightening.”

By predating his polio vaccine theory back to the late 1950s, Hooper greatly simplified his theory of AIDS origin. He ignored all those animal viruses that were placed into human tissue in the 60s and 70s, and all those dangerous viral creations that were genetically altered for cancer research, vaccine research, and secret biological warfare.

The chimp in the freezer at Fort Detrick

On February 1, 1999 Lawrence K Altman, longtime physician-writer for The New York Times, dutifully reported “the riddle of the origin of the AIDS virus has apparently been solved.” A team of researchers, headed by Beatrice Hahn at the University of Alabama, performed viral studies on three chimps in the African wild and had also studied the frozen remains of a chimp, discovered by accident in a freezer at Fort Detrick. The chimp had tested positive for HIV in 1985. On the basis of all this research, Hahn declared that a common subspecies of chimp (Pan troglodytes troglodytes) was the animal source of the virus “most closely ” related to HIV.

In a media blitz U.S. government scientists presented a phylogenetic ancestral “family tree” of primate viruses (which few people could understand) to prove that HIV was genetically descended from a chimp virus in the African bush. Molecular analysis of virus genetic data, performed by Bette Korber and the supercomputer Nirvana at the Los Alamos National Labor atory in New Mexico, indicated that HIV had jumped species from a chimp to a human in Africa around the year 1930. (Los Alamos is the official home of nuclear bomb-building, alleged Chinese spies, and the laboratory which directed secret human radiation experiments on unsuspecting civilians from the 1940s up to the beginning of the AIDS epidemic.)

Beatrice Hahn theorized that the epidemic started when a hunter cut himself while butchering chimp meat and subsequently became infected. Scientists readily accepted Hahn’s notion that the AIDS virus and its closest relatives jumped species from chimps to humans on multiple occasions, thereby explaining the origin of the three separate subtypes of HIV-1 (M, N, and O), as well as HIV-2.

Chimps in West Africa are hunted for food, as well as for medical experimentation. Young chimps are especially prized for scientific research and are usually caught by shooting their mothers. Many die from stress and inhumane conditions during capture and transport to laboratories and zoos in Western nations.

Due to all this killing, chimps are now an endangered species. During the past century the African chimp population has dropped from two million to less than 150,000. Despite the mass killing of chimps, they are still blamed for causing the worldwide epidemic of AIDS.

Beatrice Hahn is no stranger to primate theories, having worked in Gallo’s lab when he was heavily promoting the green monkey theory in the mid-1980s and the “close relationship” of the monkey virus to HIV. Now Hahn’s virus was claimed to be a closer relative than the contaminating monkey virus in Essex’ lab that formed the basis of the false green monkey theory.

Media journalists paid no attention to these discrepancies. Hahn’s new chimp findings, along with the old 1959 blood specimen, fully convinced the AIDS establishment, and an adoring media, that Africa was indeed the source of HIV and the AIDS epidemic.

The 2000 London Origin of AIDS Conference.

When Hooper’s book appeared in the fall of 1998, molecular scientists quickly used the new chimp virus data to completely discredit Hooper’s polio vaccine theory. AIDS in Africa could not be caused by a virus jumping species in the 50s if it had already jumped species back in the 1930s. Researchers refused to believe scientists could have played any role in the origin of HIV and AIDS.

Hooper bypassed the biowarfare theory by predating HIV back to the 50s. Now scientists bypassed Hooper by dating HIV back several decades earlier. The fact that there was no African epidemic until the early 1980s did not seem pertinent. To make their view official, a small group of scientists proposed an “invitation only” meeting to settle the origin matter once and for all. In October 2000 the Royal Society of London held a two-day conference on the origins of HIV. Obviously, the biowarfare theory of AIDS was not discussed. On the contrary, one professor emphatically declared “all human infectious diseases have an animal origin.” Although there never was a disease like AIDS (until scientists started to flagrantly pass viruses around to repeatedly break the species barrier ), the same professor declared that “natural transfer of these infections is a common event in animal populations.” Using the viral fragments from the 1959 specimen and comparing them with the select viruses contained in the data bank at Los Alamos , Betty Korber refined her computer calculations to establish a likely date of 1940, “with confidence levels extending from 1871 to 1955.” The Rega Institute in Antwerp estimated the transfer could have occurred between 1590 and 1760, with 1675 the most likely date.

Hooper spoke but his views were largely ignored by the molecular biologists. Preston Marx warned about more human diseases caused by viruses emerging from primates, None of the speakers mentioned what happened to the thousands of liters of animal viruses that were passed around the world by the Special Virus Cancer Program in the decade before AIDS.

Instead, the London conferees alerted the public to a new view of medical science, championed by the virologists. The “Last Word” at the conference was that “all human viral infections were initially zoonotic (animal) in origin. Animals will always provide a reservoir for viruses that could threaten human populations in the future.” And the scientists predicted: “There is still a myriad of current unknown viruses in animal populations on land, sea, and air with the potential to cause human disease.” Apparently, none of these viruses were in animal laboratories.

AIDS, cancer, genetic science and covert human medical experimentation.

Although rejected completely by most scientists, the man-made theory of AIDS is a rational explanation for the origin of HIV. This theory is partly based on an awareness of the gene-polluting activities and species jumping virus experiments of irresponsible scientists during the two decades before the epidemic.

In addition, the record clearly shows that scientists and biowarfare scientists experiment secretly on unsuspecting people. Horrific aspects of the Cold War Human Radiation Experiments attest to the fact that covert medical experimentation is not an “X-Files” fantasy or a totally paranoid belief.

It is easy to understand why researchers might want to obscure the man-made origin for AIDS and blame primates. It is now apparent that most of the major researchers promoting the African primate origin of AIDS were connected with the largely secret Special Virus Cancer Program, or are scientists involved in the transfer of viruses in animal research, particularly primate research. From the very beginning of the epidemic, researchers disclaimed any connection between AIDS and cancer, as well as any connection between HIV and animal retrovirus cancer research. In 1984, Gallo originally named HIV a cancer-causing “leukemia/lymphoma” virus. To obscure the cancer connection, the name was immediately changed to “lymphotropic” virus.

My own Kaposi’s sarcoma research, first published in medical journals in 1981, showed “cancer-associated bacteria” as possible infectious agents in “classic” KS tumors. Before HIV was discovered in 1984, additional papers in 1982 and 1983 showed similar cancer bacteria in the enlarged lymph nodes and KS tumors of gay men with “gay cancer” and AIDS. Since the 1950s, cancer-associated bacteria have been linked to viruses, as well as to mycoplasmas. This aspect of cancer research has been suppressed for decades by the cancer establishment. A history of this research and its relevancy to AIDS is the subject of my books, AIDS: The Mystery and the Solution [1984] and The Cancer Microbe: The Hidden Killer in Cancer, AIDS and Other Immune Diseases [1990].

Gallo, in his 1991 book, falsely claims that no infectious agent had ever been found in KS. The refusal of AIDS scientists to recognize cancer microbe research, published in peer reviewed scientific journals, is a further indication that the AIDS establishment seeks to control all aspects of HIV research in such a way as to never connect the origin of AIDS with previous cancer research and covert biological warfare research. This cover-up conceals the possibility that AIDS, in reality, is a new man-made form of infectious and contagious cancer.

Could a small coterie of government scientists concoct a bogus (but scientifically plausible) primate theory of AIDS origin and bamboozle the public to believe it in order to cover-up the truth?

In the 1930s the highly respected German scientific community was entirely transformed by fascist beliefs proclaiming the genetic inferiority of the Jews and the genetic superiority of the German Master Race. This Nazi takeover of science and the media eventually led to the murder of millions in the Holocaust. Could the genetic science surrounding the origin of AIDS obscure a genocidal and world depopulation program of man-made origin?

It is time for the man-made theory of HIV to be examined fairly. Proponents of this theory should not be dismissed as paranoid conspiracy theorists; and AIDS educators should educate themselves about this hidden history of AIDS and its implications for the origin of HIV. How many more species jumping viruses will we have to endure before we question the integrity and the agenda of scientists who still blissfully jump viruses between species in animal laboratories?

Lawrence K. Altman, the Times reporter who in 1999 wrote that the origin of the AIDS virus was solved, recently asked “Where did AIDS come from?” Now seemingly undecided, Altman answers, “We can only guess. Determining the answer would be important because discovering how AIDS came to be an epidemic might prevent a similar catastrophe in the future.” (“The AIDS questions that linger,” January 30, 2001).

It doesn’t take a rocket scientist to figure out how researchers could have created HIV and how they could have transferred the virus to gay and blacks in a covert medical experimentation for genocidal or population control purposes.

The secrecy and scientific disinformation surrounding the Human Radiation Experiments of the Cold War era has taught us how easily government scientists can fool the public on scientific matters. And when it comes to scientific monkey business, researchers know that most people are chumps.

Dr. Cantwell is a retired dermatologist and AIDS and cancer researcher, who has written extensively on the man-made origin of AIDS.

Source

Read more from Auricmedia:

[carousel-horizontal-posts-content-slider]