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Spartacus explains it all in great detail

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Cursed art thou to hell. You will not destroy America and the Free World, and you will not get your new world order. We will take care of that.

Below is an article by someone who calls himself Spartacus. I found it very interesting to read and for the readers of CommonSenseTV I translated it. I don't want to claim that this article is the most important thing you will ever read, but it is.

It is an extensive article that not only provides a very comprehensive description of the entire corona hoax in which we find ourselves, but also describes the disease in detail, describes the (often incorrect) treatment methods and describes the devastating effect of the so-called vaccines. It also goes into detail about the gain of function methods used in the development of the virus and the ultimate goals of Schwab and his fellow criminals. I have not been able to find a more scientific and factually substantiated overview anywhere else.

This time please no discussions about whether or not covid and sars-cov-2 exist. In my opinion, this article was written by one or more scientists, who are very well aware of all the ins and outs, including the diseases and cures, development and goals. Everything is described in great detail.

The scientific knowledge that is being displayed is beyond my cap. But what particularly intrigues me is that the author or authors of this extensive scientifically substantiated argument apparently wish to remain anonymous. My thinking is that these are scientists from the field who, because of the terrorist repressive hoax going on, are only allowed to express themselves anonymously.

We now know that the virus has never been isolated! If anyone with scientific substantiation wishes to comment, they are most welcome. Come on Bert! You haven't convinced me yet.

Please read this article. If necessary, skip the technical-scientific descriptions of the virus, the disease and the poison syringes, but the meaning of the story is crucial to absorb. Unlike that syringe. It is crucial not to ingest them!

Dear people, what is going on here is so criminal. All the great crimes, all the genocides of the past, are completely dwarfed by the terrorist acts now underway.



My name is Spartacus, and I've had enough.

We are forced to watch as America and the free world fall into unstoppable decay from a bioweapon attack. We, and countless others, have become the victims of propaganda and psychological warfare by an unelected elite against the American people and our allies.

Our mental and physical health has suffered greatly over the past year and a half. We've 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 well-being of the public from the ongoing COVID-19 pandemic.

Now we watch as the medical establishment literally injects poison into millions of our fellow human beings without saying anything against it.

We have been told we will be fired and denied our livelihood if we refuse to vaccinate. This was the last straw.

We spent thousands of hours analyzing leaked images from Wuhan, scientific documents from primary sources, and the paper trail left by the medical world.

What we have discovered should shock everyone to the depths of their souls.

First we will summarize our findings, and then we will explain them in detail. The references are placed at the end.


COVID-19 is a disease of blood and blood vessels. SARS-CoV-2 infects the lining of human blood vessels, causing them to leak into the lungs.

  • Current treatment protocols (eg invasive ventilation) are actively harming patients, accelerating oxidative stress and causing severe VILI (ventilation induced lung injuries). The continued use of respirators in the absence of proven medical benefit is mass murder.
  • The existing countermeasures are inadequate to slow the spread of what is an aerosolized and potentially wastewater-borne virus, and are nothing more than 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.
  • Authorities have denied the benefit of natural immunity to COVID-19, despite the fact that natural immunity protects against all proteins of the virus, not just one.
  • Vaccines will do more harm than good. The antigen on which these vaccines are based, SARS-CoV-2 Spike, is a toxic protein. SARS-CoV-2 may have ADE, or antibody-dependent enhancement; it's possible that current antibodies won't neutralize future strains, but instead help them infect immune cells. Vaccinating during a pandemic with a leaky vaccine also removes the evolutionary pressure to make a virus less deadly.
  • There is a large and horrific criminal conspiracy that links both Anthony Fauci and Moderna directly to the Wuhan Institute of Virology.
  • Researchers of the COVID-19 vaccine are directly linked to scientists involved in brain-computer interface (“neural lace”) technology, one of whom has been charged with taking subsidy money from China.
  • Independent researchers have discovered mysterious nanoparticles in the vaccines that shouldn't be there.
  • The entire pandemic is being used as an excuse for a massive political and economic transformation of Western society, which will enrich the rich and turn the rest of us into serfs and untouchables.

COVID-19 Pathosphysiology and Treatments:

COVID-19 is not viral pneumonia. It is a viral vascular endotheliitis and affects the lining of blood vessels, particularly the small pulmonary alveolar capillaries, leading to endothelial activation and exfoliation, coagulopathy, sepsis, pulmonary edema, and ARDS-like symptoms. This is a disease of the blood and blood vessels. The vascular system. The pneumonia 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 increased D-dimer, increased prothrombin time, increased C-reactive protein, neutrophilia, lymphopenia, hypocalcemia, and hyperferritinemia, which essentially correspond to a profile of coagulopathy and immune system hyperactivation/depletion. the immune cells.

COVID-19 can present itself as almost anything, due to the broad tropism of SARS-CoV-2 to various tissues in the vital organs of the body. While the most common initial presentation is respiratory illness and flu-like symptoms, it can present as brain inflammation, gastrointestinal illness, or even a heart attack or pulmonary embolism.

COVID-19 is more severe in people with specific co-morbidities, such as obesity, diabetes and hypertension. This is because these conditions involve endothelial dysfunction, which makes the circulatory system more susceptible to infection and injury from 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 for all infections. The number of actual infections is much, much higher. Consequently, the mortality and morbidity rate is lower. However, COVID-19 is spreading very quickly, which means that a significant number of critically ill and critically ill patients appear in a short period of time.

In those who have critically COVID-19-induced sepsis, hypoxia, coagulopathy, and ARDS, the most common treatments are intubation, injected corticosteroids, and blood thinners. This is not the right treatment for COVID-19. In severe hypoxia, cellular metabolic shifts cause ATP to be broken down into hypoxanthine, which, when oxygen is restored, triggers xanthine oxidase to produce masses of highly damaging radicals that attack tissues. This is called ischemia-reperfusion injury, and it's why the majority of people on a ventilator die. In the mitochondria, the accumulation of succinate due to sepsis does exactly the same; when oxygen is supplied again, the superoxide makes 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 begin to “rust” as a result of damage from oxidative stress. This leads to autoimmunity. Oxidized lipids appear as foreign objects to the immune system, which recognizes and forms antibodies against OSEs, or oxidation-specific epitopes. Oxidized lipids also go straight into pattern recognition receptors, triggering even more inflammation and triggering even more cells of the innate immune system to release even more destructive enzymes. This is similar to the pathophysiology of Lupus.

The pathology of COVID-19 is dominated by extreme oxidative stress and neutrophilic respiratory bursts, to the point where hemoglobin is no longer able to carry oxygen due to heme iron being stripped from heme by hypochlorous acid. No amount of extra oxygen can oxygenate the 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 management system that regulates fluid volume in the body and in the bloodstream (ie osmolarity) by controlling salt retention and excretion. This protein, ACE2, is ubiquitous in every part of the body that interacts with the circulatory system, especially in vascular endothelial cells and pericytes, brain astrocytes, renal tubules and podocytes, pancreatic islet cells, bile duct and intestinal epithelial cells, and testicular vas deferens, which SARS-CoV-2 can infect anyone, not just the lungs.

SARS-CoV-2 infects a cell as follows: SARS-CoV-2 Spike undergoes a conformational change in which the S1 trimers flip up and extend, snapping onto ACE2 bound to the cell surface. TMPRSS2, or transmembrane protease serine 2, severs the spikes' heads, exposing the S2 star-shaped subunit inside. The rest of the Spike undergoes a conformational change that causes it to unfold like an extension ladder and settle into the cell membrane. It then folds back on itself, pulling the viral membrane and the cell membrane together. The two membranes fuse together, with the proteins of the virus migrating to the cell surface. The SARS-CoV-2 nucleocapsid penetrates the cell, spreads the genetic material and begins the viral replication process, hijacking the cell's own structures to produce more virus.

SARS-CoV-2 spike proteins embedded in a cell can fuse human cells to form syncytia/MGCs (multinuclear giant cells). They also have other pathogenic, harmful effects. SARS-CoV-2's viroporins, such as the Envelope protein, act as calcium ion channels, bringing calcium into infected cells. The virus suppresses the natural interferon response, leading to delayed inflammation. The N protein of SARS-CoV-2 can also directly activate the NLRP3 inflammatory mechanism. It also suppresses the Nrf2 antioxidant pathway. The suppression of ACE2 by binding to Spike causes an accumulation of bradykinin that would otherwise be degraded by ACE2.

This constant influx of calcium into the cells leads to (or is associated with) noticeable hypocalcemia, or low blood calcium, especially in people with vitamin D deficiency and pre-existing endothelial dysfunction. Bradykinin increases the activity of cAMP, cGMP, COX and phospholipase C. This results in prostaglandin release and a greatly increased intracellular calcium signaling, which promotes a very aggressive release of ROS 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 for endothelial nitric oxide synthase, destroying it and “uncoupling” the enzymes, causing nitric oxide synthase to produce more superoxide instead. This occurs in a positive feedback loop until the bioavailability of nitric oxide in the circulation is exhausted.

Dissolved nitric oxide gas continuously produced by eNOS has many important functions, but it is also antiviral against SARS-like coronaviruses by inhibiting palmitoylation of the viral Spike protein and making it more difficult to bind to host receptors. The loss of NO allows the virus to multiply in the body with impunity. People with disrupted endothelium (hypertension, diabetes, obesity, old age, African American race) have problems with the redox balance to begin with, giving the virus an advantage.

Due to the extreme cytokine release triggered by these processes, the body calls a large amount 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 swallowing invaders and attempting to attack them with enzymes that produce powerful oxidants, such as 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 peroxidation.

Neutrophils have a mean trick. They can also eject these enzymes into the extracellular space, where they continuously spew 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 even quite severe NETosis.

Hypochlorous acid that builds up in the bloodstream begins to bleach the iron from the heme and competes for the O2 binding sites. Red blood cells lose the ability to carry oxygen, causing the patient to turn blue in the face. Unprocessed iron, hydrogen peroxide and superoxide in the bloodstream undergo the Haber-Weiss and Fenton reactions, creating highly reactive hydroxyl radicals that forcibly extract electrons from surrounding fats and DNA, causing them to severely oxidize.

This condition is not unknown to medical science. The actual name for all this is acute sepsis.

We know this is happening in COVID-19 because people who have died from the disease have noticeable ferroptosis signatures in their tissues, as well as several other oxidative stress markers such as nitrotyrosine, 4-HNE, and malondialdehyde.

When you intubate someone with this condition, you detonate a free-radical bomb by feeding the cells with O2. It's a catch-22, because we need oxygen to make Adenosine Triphosphate (ie to live), but O2 is also the precursor of all these harmful radicals that lead to lipid peroxidation.

The appropriate treatment for severe COVID-19 sepsis is non-invasive ventilation, steroids, and antioxidant infusions. Most of the drugs reused for COVID-19 that show some benefit in rescuing critically ill COVID-19 patients are antioxidants. N-acetyl cysteine, melatonin, fluvoxamine, budesonide, famotidine, cimetidine, and ranitidine are all antioxidants. Indomethacin prevents iron-driven oxidation of arachidonic acid to isoprostanes. There are powerful antioxidants like apocynin that haven't even been tested on COVID-19 patients that could denerve neutrophils, prevent lipid peroxidation, restore endothelial health, and restore tissue oxygenation.

Scientists who know about pulmonary neutrophils, ARDS, and redox biology have known or suspected much of this since March 2020. In April 2020, Swiss scientists confirmed that COVID-19 was vascular endotheliitis. By the end of 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 new, and yet, for the most part, it has not been acted upon. Physicians continue to use harmful intubation techniques with high PEEP settings despite high lung compliance and poor oxygenation, resulting in the death of a untold number of critically ill patients from medical malpractice.

Due to the way they are constructed, Randomized Control Trials will never demonstrate any benefit for any antiviral drug against COVID-19. Not Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The reason for this is simple; for the patients they recruited for these studies, such as Oxford's ridiculous 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 dwindled to almost nothing. If a person is about 10 days post-exposure and has been symptomatic for five days, there is hardly any virus left in their body, just cellular damage and disruption that has triggered a hyperinflammatory response. It is from this group that the clinical trials for antiviral drugs are almost exclusively recruited.

In these trials, they give antivirals to critically ill patients who have no virus in their bodies, only a delayed hyperinflammatory response, and then absurdly claim that antivirals are of no use in treating or preventing COVID-19. These clinical studies 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 deliver only flatline shocks, and then absurdly claiming that defibrillators are of no medical use if the patients refuse to rise from the dead. The intervention is too late. These antiviral drug trials show a systematic, blatant selection bias. They provide treatment that is meaningless to the specific cohort they are enrolling in.

India went against WHO's instructions and ordered prophylactic use of Ivermectin. They have almost completely eradicated COVID-19. The Indian Bar Association in Mumbai has launched criminal charges against WHO Chief Scientist Dr. Soumya Swaminathan for advising against the use of Ivermectin.

Ivermectin is not an “horse wormer”. Yes, it is sold in the form of a veterinary paste as an animal wormer. It has also been available in pill form for humans for decades, as an antiparasitic drug.

The media has falsely claimed that because Ivermectin is an anti-parasitic agent, it has no use as an anti-virus. This is incorrect. Ivermectin is useful as an antiviral agent. It blocks importin and thus prevents nuclear import, preventing the virus from accessing the cell nuclei. Many drugs currently on the market have multiple mechanisms of action. Ivermectin is one such medicine. It is both antiparasitic and antiviral.

In Bangladesh, Ivermectin costs $1,80 for a full course of 5 days. Remdesivir, which is toxic to the liver, costs $3.120 for a 5-day course of the drug. Billions of dollars of totally useless Remdesivir were sold to our governments at taxpayer expense, and it turned out to be totally useless for the treatment of hyper-inflammatory COVID-19. The media has paid little attention to this.

The opposition to the use of generic Ivermectin is not based on science. It is purely financially and politically motivated. An effective vaccine-less intervention would jeopardize the hasty FDA approval of patented vaccines and drugs that could potentially rake in billions of dollars in revenue for the pharmaceutical industry.

The majority of the public is scientifically illiterate and doesn't understand what all this means, thanks to a pathetic education system that has raised them incorrectly. You'd be lucky if you can find 1 in 100 people who have the faintest idea what this all means.

COVID-19 Transmission:

COVID-19 is transmitted by air. The WHO has compromised China by claiming that the virus is only transmitted through droplets. Our own CDC absurdly claimed that it was transmitted primarily through fomite-to-face contact, which, given Wuhan's rapid spread to the rest of the world, would have been physically impossible.

The ridiculous belief in fomite-to-face as the primary mode of transmission led to the use of surface sanitizing protocols that wasted time, energy, productivity and sanitizers.

The 2-meter guidelines are absolutely useless. The minimum safe distance to protect against an aerosol virus is to be more than 2 meters from an infected person, no closer. Realistically, no public transportation is safe.

Surgical masks do not protect you from aerosols. The virus is too small and the filter medium has too large openings to filter it out. They may catch respiratory droplets and prevent the virus from being shed by someone who is sick, but they don't filter a cloud of infectious aerosols if someone were to walk in that cloud.

The minimum protection against this virus is literally a P100 respirator, a PAPR/CAPR, or a 40mm NATO CBRN respirator, ideally in combination with a full tyvek or tychem suit, gloves and overshoes, with all holes and cracks taped.

Live SARS-CoV-2 may be detectable in sewage and oral-faecal transmission may occur. During the SARS outbreak in 2003, in the Amoy Gardens incident, hundreds of people were infected by aerosolized fecal material that rose 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 take the evolutionary pressure off the virus to become less lethal. It also means that the vaccinated are perfect carriers. In other words, those who are vaccinated pose a threat to the unvaccinated, not the other way around.

All COVID-19 vaccines currently in use have undergone minimal testing, with highly accelerated clinical trials. Although they appear to limit severe disease, the long-term safety profile of these vaccines remains unknown.

Some of these so-called "vaccines" use an untested new technology that has never been used in vaccines before. Traditional vaccines use weakened or killed virus to stimulate an immune response. Moderna's and Pfizer-BioNTech's vaccines don't. They would consist of an intramuscular injection of a suspension of lipid nanoparticles filled with messenger RNA. The way they elicit an immune response is by merging with cells in the vaccine recipient's shoulder, undergoing endocytosis, releasing their mRNA payload into those cells, and then using the ribosomes in those cells to produce locally modified to synthesize SARS-CoV-2 spike proteins.

These modified spike proteins then migrate to the cell surface, where they are anchored in place by a transmembrane domain. The adaptive immune system detects the non-human viral protein expressed by these cells and then forms antibodies against that protein. This would protect against the virus by training the adaptive immune system to recognize and produce antibodies against the Spike on the actual virus. J&J and AstraZeneca's vaccines do something similar, but use an adenovirus vector to deliver genetic material instead of a lipid nanoparticle. These vaccines have been produced or validated using fetal cell lines HEK-293 and PER.C6, which people of certain religious beliefs may strongly object to.

The vaccine manufacturers claim that the vaccine remains in the shoulder cells and that the SARS-CoV-2 Spike produced and expressed by these cells from the genetic material of the vaccine 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 found that the lipid nanoparticles and mRNA from the Pfizer vaccine did not stay in the shoulder, but bioaccumulated in many different organs, including the reproductive organs and the adrenal glands, meaning the modified Spike manifested itself literally everywhere. comes. These lipid nanoparticles can cause anaphylaxis in an unlucky few, but more troubling is the unregulated expression of Spike in several somatic cell lines far from the injection site and its unknown consequences.

Messenger RNA is usually consumed immediately after it is produced in the body, where it is translated into a protein by a ribosome. The mRNA from the COVID-19 vaccine is produced outside the body long before it is translated by a ribosome. In the meantime, it can be damaged if not kept enough. When a ribosome tries to translate a damaged strand of mRNA, it can get stuck. 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 rotation, such as nerve cells, this can lead to decreased protein synthesis, cytopathic effects, and neuropathies.

Certain proteins, including SARS-CoV-2 Spike, have proteolytic cleavage sites that actually look like little dotted lines that say "cut here," which attract a living organism's own proteases (essentially molecular scissors) to cut them. It is possible that S1 is proteolytically cleaved from S2, allowing active S1 to enter the bloodstream, while the S2 “stalk” remains in the membrane of the cell that expressed the protein.

SARS-CoV-2 Spike has a superantigenic region (SAg), which can promote extreme inflammation.

One study found that anti-Spike antibodies function like autoantibodies, attacking the body's own cells. People who have been vaccinated with COVID-19 vaccines have developed blood clots, myocarditis, Guillain-Barre syndrome, Bell's Palsy and multiple sclerosis flare-ups, suggesting the vaccine promotes autoimmune responses against healthy tissue.

SARS-CoV-2 Spike does not bind to ACE2 alone. It was also suspected to have regions that bind to basigin, integrins, neuropilin-1, and bacterial lipopolysaccharides. SARS-CoV-2 Spike on its own can bind any of these things and act as a ligand for them, triggering unspecified and probably highly pro-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 trait for the Spike, giving it a high degree of cell tropism. No wild-type SARS-like coronavirus related to SARS-CoV-2 possesses this trait, making it highly suspect, and perhaps a sign of human manipulation.

SARS-CoV-2 Spike has a prion-like domain that increases its infectivity.

The Spike S1 RBD can bind to heparin-binding proteins and promote amyloid aggregation. In humans, this could lead to Parkinson's, Lewy Body Dementia, early Alzheimer's, or several other neurodegenerative diseases. This is very worrying because SARS-CoV-2 S1 is capable of damaging the blood-brain barrier and entering the brain. It is also able to increase the permeability of the blood-brain barrier to other molecules.

SARS-CoV-2, like other beta-coronaviruses, can exhibit Dengue-like ADEs, or antibody-dependent enhancement of the disease. For those who don't know, some viruses, including beta-coronaviruses, have a feature called ADE. There is also such a thing as “Original Antigenic Sin” where the body prefers to make antibodies based on previously encountered virus strains over newly found virus strains.

In ADE, antibodies from a previous infection become non-neutralizing due to mutations in the virus proteins. These non-neutralizing antibodies then act like Trojans, allowing live, active virus to be drawn into macrophages via their Fc receptor pathways, allowing the virus to infect immune cells it hadn't been able to infect before. This is known to happen in dengue fever; when a person gets sick with dengue fever, recovers and then contracts another strain, he can get very, very sick.

If someone is inoculated with mRNA based on the Spike of the original Wuhan strain of SARS-CoV-2 and then infected with a future mutated strain of the virus, they can become seriously ill. In other words, it is possible for vaccines to make a person hypersensitive to disease.

There is a precedent for this in recent history. Sanofi's Dengvaxia vaccine against dengue fever failed because it caused immune sensitization in people whose immune systems could not withstand dengue fever.

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 eosinophilic infiltration in their lungs.

We were told that SARS-CoV-2 mRNA vaccines cannot be incorporated into the human genome because messenger RNA cannot be converted to DNA. This is incorrect. There are elements in human cells, called LINE-1 retrotransposons, that can indeed integrate mRNA into a human genome by endogenous reverse transcription. Because the mRNA used in the vaccines is stabilized, it lingers longer in the cells, increasing the chances of this happening. If the gene for SARS-CoV-2 Spike is integrated into a part of the genome that is not silent and actually expresses a protein, it is possible that people who take this vaccine will have SARS-CoV-2 continuously for the rest of their lives. express spike from their somatic cells.

By vaccinating people with a vaccine that causes their bodies to produce Spike in situ, they are inoculated with a pathogenic protein. A toxin that can lead to inflammation, heart problems and an increased risk of cancer in the long term. In the long run, it can also lead to neurodegenerative diseases.

Absolutely no one should be forced to take this vaccine under any circumstances, and in fact the vaccination campaign should 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 laundered through NGOs.

Ralph Baric is a virologist and SARS expert at UNC Chapel Hill in North Carolina. He's the one Anthony Fauci referred to when he insisted before Congress that if any research into how SARS works, it was in North Carolina.

This was a lie. Anthony Fauci lied to Congress. A crime.

Ralph Baric and Shi Zhengli are colleagues and have written articles together. Ralph Baric guided Shi Zhengli in his manipulation techniques, especially serial passage, resulting in a virus that appears to have arisen naturally. In other words, undeniable bioweapons. Serial passage in humanized hACE2 mice may have generated something like SARS-CoV-2.

Funding for the gain-of-function research being conducted at the Wuhan Institute of Virology came from Peter Daszak. Peter Daszak leads an NGO called EcoHealth Alliance. EcoHealth Alliance received millions of dollars in grants from the National Institutes of Health/National Institute of Allergy and Infectious Diseases (i.e., Anthony Fauci), the Defense Threat Reduction Agency (part of the United States Department of Defense), and the United States Agency for International Development. NIH/NIAID contributed several million dollars, and DTRA and USAID each contributed tens of millions of dollars to this research. In total, it was more than a hundred million dollars.

EcoHealth Alliance outsourced these grants to the Wuhan Institute of Virology, a lab in China with a highly questionable reputation for safety and poorly trained staff, so they could conduct gain-of-function research, not in their fancy P4 lab, but in a level 2 lab where technicians wore nothing more 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 lab animals. Why anyone would outsource this dangerous and delicate work to the People's Republic of China, a country notorious for industrial accidents and massive explosions that have claimed hundreds of lives, is beyond me, unless the intention was to deliberately cause a pandemic.

In November 2019, three technicians from the Wuhan Institute of Virology developed symptoms consistent with a flu-like illness. Anthony Fauci, Peter Daszak, and Ralph Baric knew immediately what had happened, because there are back channels between this lab and our scientists and officials.

December 12, 2019, Ralph Baric signed a Material Transfer Agreement (essentially an NDA) to receive Coronavirus mRNA vaccine related materials jointly owned by Moderna and NIH. It wasn't until a whole month later, on January 11, 2020, that China reportedly sent us the sequence of what would become known as SARS-CoV-2. Moderna claims, rather absurdly, that they have developed a working vaccine based on this sequence in less than 48 hours.

Stephane Bancel, the current CEO of Moderna, was previously CEO of bioMerieux, a French multinational company specializing in medical diagnostic technology, founded by one Alain Merieux. Alain Merieux was one of the individuals who contributed to the construction of the P4 laboratory of the Wuhan Institute of Virology.

The sequence reported as the closest relative of SARS-CoV-2, RaTG13, is not a true virus. It's a forgery. It was created by manually entering a gene sequence into a database to cover up the existence of SARS-CoV-2, which is most likely a gain-of-function chimera published in the Wuhan Institute of Virology. was produced and either accidentally leaked or intentionally released.

The animal reservoir of SARS-CoV-2 has never been found.

This is not a "theory" of a conspiracy. It is a criminal conspiracy, with people involved in the development of Moderna's mRNA-1273 being directly linked to the Wuhan Institute of Virology and their "gain-of-function" research with very little or no degree of separation. The paper trail is clear.

The lab leak theory has been suppressed because pulling that thread inevitably leads to the conclusion that there is enough circumstantial evidence to link Moderna, the NIH, the WIV, and both the vaccine and the origin of the virus. bring. In a normal country, this would have immediately led to the world's largest RICO and mass murder case. Anthony Fauci, Peter Daszak, Ralph Baric, Shi Zhengli, and Stephane Bancel, and their accomplices, are said to have been charged and prosecuted to the fullest extent of the law. Instead, billions of our tax dollars were allocated 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 used? Intravenous Vitamin C. An Antioxidant. Which, as described above, is a fully valid treatment for COVID-19-induced sepsis, and indeed, is now part of the MATH+ protocol developed by Dr. Paul E. Marik.

The FDA has banned ranitidine (Zantac) due to alleged NDMA (N-nitrosodimethylamine) contamination. Ranitidine is not only an H2 blocker that is used as a gastric acid inhibitor, but also has a powerful antioxidant effect, which scavenges hydroxyl radicals. This makes it useful in the treatment of COVID-19.

The FDA has also tried to remove N-acetyl cysteine, a harmless amino acid supplement and antioxidant, from the shelves, forcing Amazon to remove it from their online store.

This leaves us with a chilling question: Has the FDA deliberately suppressed antioxidants useful for treating COVID-19 sepsis as part of a criminal conspiracy against the American public?

The establishment partners with and facilitates the worst criminals in human history, actively suppressing non-vaccine treatments and therapies to force us to inject the products of these criminals into our bodies. This is absolutely unacceptable.

COVID-19 Vaccine Development and Links to Transhumanism:

This section examines some more speculative aspects of the pandemic and the response of the medical and scientific establishment to it, as well as the disturbing links between scientists involved in vaccine research and scientists whose work has involved merging nanotechnology with living cells.

On June 9, 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 grants from the US Department of Defense, notably the military think tanks DARPA, AFOSR and ONR, as well as NIH and MITRE. His specialty is using silicon nanowires instead of patch clamp electrodes to monitor and modulate intracellular activity, something he has been working on at Harvard for the past twenty years. He is said to have worked on silicon nanowire batteries in China, but none of his colleagues remember ever working on battery technology in his life; all his research relates to bionanotechnology, or the mixing of nanotech with living cells.

The indictment related to his collaboration with the Wuhan University of Technology. He had taken money, against the terms of his DOD grants, from the People's Republic of China's "Thousand Talents" scheme, a program the Chinese government uses to bribe Western scientists into sharing classified R&D information that can be exploited by the PLA for strategic advantage.

Charles Lieber describes in his own papers the use of silicon nanowires for brain-computer interfaces, or “neural lace” technology. His work describes how neurons can endocytose whole silicon nanowires or parts thereof, allowing for the monitoring and even modulation of neuronal activity.

Charles Lieber was a colleague of Robert Langer. Together with Daniel S. Kohane, they worked on a paper describing artificial tissue dishes that can be implanted in a human heart to remotely monitor its activity.

Robert Langer, an MIT alumnus and expert in nanotech drug delivery, is one of the co-founders of Moderna. His net worth now stands at $5,1 billion thanks to the sale of Moderna's mRNA-1273 vaccine.

Both Charles Lieber's and Robert Langer's bibliographies essentially describe techniques for improving man, ie transhumanism. Klaus Schwab, the founder of the World Economic Forum and the architect behind the so-called “Great Reset”, has long talked about the “mixing of biology and machines” in his books.

Since these revelations, independent researchers have learned 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 lab mice when injected into their brains. Indeed, given the tendency of SARS-CoV-2 Spike to compromise the blood-brain barrier and increase its permeability, it is the perfect protein to prepare brain tissue for the 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 will develop brain-computer interface technologies for the military, especially non-invasive, injectable systems that cause minimal damage to brain tissue when removed. It is believed that this technology will be used to heal wounded soldiers with traumatic brain injuries, direct brain control of prosthetic limbs, and even new abilities such as piloting drones with one's own mind.

Several methods have been proposed to achieve this, including optogenetics, magnetogenetics, ultrasound, implanted electrodes, and transcranial electromagnetic stimulation. In all cases, the goal is to gain read or write power over neurons, either by stimulating and sensing them or by making them particularly sensitive to stimulation and sensing.

However, the idea of ​​widespread use of BCI technology, such as Elon Musk's Neuralink device, raises many concerns about privacy and personal autonomy. Reading neurons is problematic enough on its own. Wireless brain computer interfaces can interact with current or future GSM wireless infrastructure, raising concerns about the safety of neurological data. A hacker or other malicious person could compromise such networks to obtain people's brain data, then exploit it for nefarious purposes.

However, a device capable of writing to human neurons, not just reading them, raises another, even more serious set of ethical problems. A BCI capable of altering the contents of one's mind for harmless purposes, such as projecting a heads-up display onto the brain's visual center or sending audio to one's auditory cortex, would theoretically also be able to and personality, or perhaps even subjugate one's will and make him completely 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 settle for life in a literal doghouse.

BCIs could be used to unscrupulously alter the perception of basic things like emotions and values, by altering people's thresholds for satiety, happiness, anger, disgust, and so on. This is not unimportant. A person's entire behavioral regimen can be altered by a BCI, including things like suppressing their appetite or craving almost anything in Maslow's hierarchy of needs.

Anything is possible when you have direct access to someone's brain and its contents. Someone who is obese may develop an aversion to food. A person who is involuntarily celibate can have their libido shut down so that they no longer even desire sex. Someone who is racist may be forced to delight in living with people of a different race. Someone who is violent may be forced to be meek and submissive. These things may sound good to you if you are a tyrant, but to normal people the idea of ​​personal autonomy being overruled to such an extent is appalling.

For the wealthy, neural laces would be an unparalleled boon, giving them the ability to increase their intelligence with neuroprostheses (i.e., an “exocortex”), giving irresistible commands directly into the minds of their BCI-equipped servants, even physically or sexually abusive orders they would normally refuse.

If the vaccine is a method of surreptitiously injecting an injectable BCI into millions of people without their knowledge or consent, then we are witnessing the rise of a tyrannical regime like never before seen on this planet, a regime that fully intends to deprive every man, woman and child of his free will.

Our flaws are what makes us human. A utopia achieved by depriving people of their free will is not a utopia at all. It's a monomaniac nightmare. Moreover, the people who rule over us are types of the Dark Triad who cannot be trusted with such power. Imagine being beaten and sexually abused by a rich and powerful psychopath and forced to laugh because your nervous system leaves you no choice but to obey your master.

The elites are taking advantage of this technology without giving people any space to question the social or ethical consequences, or to set up regulatory frameworks that ensure that our personal agency and autonomy are not overruled by these devices. . They do this because they secretly dream of a future where they can treat you worse than an animal and not even fight you back. If this diabolical plan is carried through, it will mean the end of humanity as we know it.


The current pandemic has been caused and perpetuated by the establishment, using a virus developed in a PLA-affiliated Chinese biowarfare laboratory, with the aid of US taxpayers' money and French expertise.

This research was conducted under the utterly ridiculous euphemism of "gain-of-function" research, which is supposedly conducted to determine which viruses have the greatest potential for zoonotic spread and to provide preventative vaccinations or surveillance.

Gain-of-function threat research, also known as “dual-use research of concern,” or DURC, is bioweapons research by a different, kinder-sounding name, just to avoid the taboo of calling it what it actually is. It's always been bioweapons research. The people conducting this research are well aware that they are taking wild pathogens that are not contagious to humans and making them more contagious, often with grants from military think tanks encouraging them to do so.

Their motives are clear and bright to anyone who has paid attention. These megalomaniacs have looted the pension funds of the free world. Wall Street is insolvent and has been in an ongoing liquidity crisis since late 2019. The goal now is to exercise total, complete physical, mental and financial control over humanity before we realize how much extorted we have been by these maniacs.

The pandemic and its response served multiple purposes for the Elite:

  • Concealing a depression caused by the usurious looting of our economies by rentier capitalists and absentee owners who produce absolutely nothing of value to society. Instead of a very predictable Occupy Wall Street Part II, the elites and their minions could appear on television portraying themselves as wise and all-powerful saviors rather than the marauding cabal of despicable land pirates that they are.
  • Destroying small businesses and eroding the middle class.
  • Shifting trillions of dollars of wealth from the American public into the pockets of billionaires and special interests.
  • Insider trading, buying shares in biotech companies, and shorting brick and mortar companies and travel companies, aiming to collapse personal commerce and tourism and replace it with electronic commerce and services.
  • Creating a casus belli for war with China, encouraging us to attack them, wasting American lives and treasure, and bringing us to the brink of nuclear Armageddon.
  • Setting up 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, unemployment and food shortages, using the false guise of a vaccine to force cooperation.
  • Any of these things would be a brutal rape of Western society.
  • All things considered, it is unimaginable; it is a complete reversal of our most cherished values.

What is the purpose of all this? One can only speculate about the motives of the perpetrators, but we have some theories.

The Elites seek to climb the ladder, erase upward mobility for large segments of the population, eradicate political opponents and other "undesirables", and lead the rest of humanity on a leash, by restricting our access to certain rationing goods and services that they have labeled as “highly burdensome”, such as car use, tourism, meat consumption, etc. Of course, they will continue to have their own luxuries, as part of a strict caste system akin to feudalism.

Why are they doing this? Easy. The Elites are Neo-Malthusians and believe that we are overpopulated and that the depletion of resources will cause civilization to collapse within a few decades. They are not necessarily wrong in this belief. We are overpopulated, and we consume too many resources. But orchestrating such a gruesome and murderous coup in response to a looming crisis demonstrates that they have nothing but the utmost contempt for their fellow man.

For those who participate in this disgusting farce without any understanding of what they are doing, we have one word for you. Stop. You are causing irreparable damage to your country and to your fellow citizens.

For those who read this warning and know and understand what they are doing and how millions of innocent people are being unjustly injured, we have a few more words.

Cursed art thou to hell. You will not destroy America and the Free World, and you will not get your new world order. We will take care of that.


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