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Are They TRYING To Kill You?

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Are They TRYING to Kill You, or Are They Just Corrupt, Avaricious, and Stupid?

Governments [and their bureaucracies] lie. They lie all the time. If they told people the truth, they wouldn’t last very long. –Legendary historian Dr. Howard Zinn

We know from this meticulous independent analysis of Israeli Government health data that someone who gets the Pfizer mRNA jab is 14.6 times more likely to die in the next weeks than someone in a statistically matched group who doesn’t get jabbed. That’s 14.6 times more likely to die per day.

That means the mRNA jabs would have to protect you 100% from COVID death for nearly three years for them to be a break-even proposition. You know the jabs don’t protect you for three years because they’re already telling you you need to risk another jab and it hasn’t even been one year.

But it’s worse than that. This analysis doesn’t include the many vaccine side-effects because the official Israeli records don’t include them. While many of these side effects may not kill you, they may leave you crippled in various ways and mark you for life. Bell’s Palsey, Guilian Barr Syndrome, stroke, heart inflammation, etc. for just a few examples.

And what happens after those dangerous initial weeks?

We don’t know for sure because there aren’t even those meticulous Israeli Government vaccine-related death records after that initial period.

We can, however, get a pretty good idea from the VAERS (Vaccine Adverse Event Reporting System) and equivalent EURO data bases where some — best estimate, only about 10% — of the vaccine related deaths and side-effects are reported. Even that meager 10% reported through VAERS alone shows completely unprecedented levels of vaccine related injury and death – – –

VAERS data released Friday [August 24, 2021] by the CDC showed a total of 623,343 reports of adverse events from all age groups following COVID vaccines, including 13,627 deaths [an increase of 559 over the data released last week] and 84,466 serious injuries [up 3,416 compared with the previous week] between Dec. 14, 2020 and Aug. 20, 2021. –COVID Vaccine Injury Reports Jump by 27,000 in One Week

Based on the VAERS 10% factor, those figures imply 6,233,430 adverse vaccine events, 844,660 serious injuries and 136,270 deaths. So far.

So, even though seriously underestimated, both VAERS and the EU verson reveal an unprecedented — but still only short-term — continuation of jab-related death and serious — often incurable — side-effects and injuries.

Unfortunately, the really long-term negative effects can’t be detected, verified, and analyzed because those require long-term tracking and verification.

How long-term is “long-term?”

In general, because of the major potential harm vaccines can do when widely administered, the normal “long-term” necessary to collect, verify, and analyze vaccine data is about six years but may be as long as 12 years. That means a minimum of six years of long-term data are required before a vaccine’s safety can be legitimately certified.

And keep in mind, such vaccine safety approval is actually a rare event. About 78% of experimental vaccines don’t make the grade.

Do we have six years of long-term data on the mRNA jabs?

So, have they been LEGITIMATELY certified “safe?”

OK, so they’re still “experimental,” regardless of FDA shenanigans.

So, first iteration, “Are They TRYING to Kill You or Are They Just Corrupt and Stupid?

Either way, that means we’re likely in for some unpleasant surprises in the next five years and possibly many more years to come.

What sorts of “unpleasant surprises?”

There are at least two longer-term problems caused by the experimental mRNA vaccines — Pfizer, Moderna, AstraZenica, J&J, etc. — predicted by virologists, for which there is significant and developing data — and another problem that’s a lot more unpleasant. There may be others.

The first problem is what’s being called “the leaky vaccine” problem. Since their true efficacy has been lowered from the fake P.R. mid 90% range to a current low in the 30% “leaky” range, these mRNA jabs turn vaccinated folks into factories producing new mutated versions of COVID. This explains the rapid development of Delta, Mu, etc.

The second problem is called antiboddy dependent enhancement or ADE. ADE may cause mRNA vaccinated folks to have much more serious disease when later exposed to the actual COVID virus, especially if it’s a variant.

Further, this research shows that vaccinated folks may be overrun with virus, carrying 251 times as much virus as unvaccinated folks, and thus have the potential to become so-called “super-spreaders.”

But there’s a third problem, apparently unique to mRNA, which has caused animal tests — waived for the mRNA COVID vaccines — to fail. The animal subjects died of a plethora of causes, and may have been rendered incapable of reproduction.

It’s like this – – –

The mRNA jabs program your own cells to produce toxic COVID spike protein. They were specifically designed to do that. It’s these self-produced spike proteins that cause your immune system to produce antibodies.

But these experimental “vaccines” don’t always stay in your deltoid muscle — the usual injection site — like they’re supposed to. They circulate throughout your body, causing cells in many locations to produce the toxic COVID “spike protein.”

According to one Canadian doctor, this happened in 62% of his mRNA vaccinated patients.

But just like the original, the escaped toxic self-produced spike proteins damage cells in many organs — especially in the circulatory system — throughout the body, doing often irreversible micro-damage.

This explains the increased occurrence of circulatory problems like heart inflamation in mRNA vaccinated young men. It would in fact explain the wide range of effects of both COVID itself — and mRNA vaccine side-effects.

The problem is that the circulatory system produces micro-clots in response to the spike-induced cell damage. In many organs, the spike-caused damage doesn’t heal and the clots may block capillaries, thus starving parts of various organs of oxygen. For example, if in the brain, this would cause micro-strokes.

This sort of spike and micro-clot damage is very difficult to diagnose because, well, it’s micro. So far there’s only one test, normally used to diagnose large clots but it works even if there are a bunch of smaller clots as well.

That test is called the D-DIMER test, and if you’ve had the jab or know someone who has, and are having weird symptoms — often written-off as psychological — push for the D-DIMER test.

But we only know about some — and only some — of these mRNA-caused problems because every once-in-awhile, one of them manages to escape the establishment’s vaccine-protective cone-of-silence and then also manages to avoid the rampant media/internet censorship and character assassinations.

To get a clear picture of the net benefit of risking an mRNA jab, any ill-effects during that six-year period must be discovered, analyzed, quantified, and added to the 14.6x death-risk danger which only covers the deaths — not the other side-effects — during the tracked period immediately after the jab(s).

Further, the additional deaths, maimings, etc. only show up in longitudinal studies conducted over time, normally at least six years for vaccines remember. But we don’t have the six-year long-range experience and data to recognize and analyze those long-term effects. The medical establishment is just beginning to react to the clot dangers for example.

So it’s clear, Mr. Biden has it backwards. Given that the leaky vaccines propagate mutated variants, that ADE makes the vaccinated more susceptible to variants and getting seriously ill, and that vaccinated folks have a lot more virus in their nasal cavities and may become “super spreaders,” we don’t need to “protect the vaccinated from the unvaccinated.” The question is, “how do we protect the unvaccinated — in fact everyone — from the vaccinated?

But even if the experimental mRNA vaccines were safe and effective — we now know they’re neither — there are still at least three reasons not to get jabbed with them anyway.

FIRST: For nearly everyone under the age of 60, COVID itself is of very little rational concern, less concern than seasonal flu for example — especially when measured against the dangers and expense of the jab. This is spectacularly true for children who hardly ever contract it — and the very few who do almost never die from it. And despite the outlandish media fear-mongering, children don’t pass it on to grandpa.

SECOND: There are extremely effective non-vaccine treatment alternatives with long track records of safety. According to their own rules, that means the F.D.A. is not permitted to grant emergency status to untested vaccines. Of course they did anyway. Afterall, if we’ve learned anything in the last year-and-a half, it’s that the rules only apply to us, not to them.

THIRD: We also know that natural immunity is at least 13 times more effective at stopping COVID-19 and it’s spread than the jab and yet the health bureaucracy and industry wants to vaccinate those with natural immunity anyway — including the kids — despite the 14.6x-plus death-danger from the vaccine.

Why? Do they want to kill you or are they just stupid? Or is there more to it? Are they avaricious? Is it the money?

The real tell is that whoever’s calling the shots on this farce is CENSORING everyone who calls attention to their numerous mistakes, misprints, unintended bias, fudges, fibs, misrepresentations, outright lies, fraud, etc. Some folks call such checking, testing, analyzing — and taking the time to do it — “Due Process of Science.”

NOTE TO DR. FAUCI: Without Due Process, you can’t claim it’s science.

And they’re censoring everyone from Dr. Robert Malone, who developed the mRNA technology used in these “vaccines” while he was working at the Salk Institute of Virology, to progressive star Dr. Naomi Wolf who’s been trying to warn us for over a year. And nearly everyone in between.

In the good old days, resorting to censorship was the kiss of death. The censorship itself was taken as prima facie proof the censor couldn’t rationally deal with challenges and was, well, just completely full of it.

You can draw your own conclusions.

So, are they trying to kill you or are they just corrupt, avaricious and stupid?

 

 

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12 COMMENTS

  1. Warning. It does not seem user friendly if you try to copy/paste parts of it, and opens up to another link, which I am unsure of, so will not click on.
    Nor can I find it in google so probably shadow banned, though it is strange as I can find that others have searched for it when typing into my search box.

    One can read it all on that link.
    A very comprehensive information of just what is Covid and gives great simple detail.

    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.

    The Spartacus Letter
    https://www.docdroid.net/kZZXcGS/covid-19-the-spartacus-letter-pdf

    15 pages of the letter,
    41 pages, in total with numerous sources and links,

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    • Essential reading. You can skim through the highly technical scientific / medical passages and anyone with two or more functioning brain cells should be able to understand the rest. We should all be sending this to politicians, I have, though of course many of them give every impression that two functioning brain cells would be a struggle for them.

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  2. It’s all about both, yes they are trying to kill off many of the world population. Bill Gates has for a long time talked about the world over population etc etc, but the thought of the money is a huge benefit to Bill Gates and others. He and his cohorts are the satans of the time. Hitler and Russia and and and others rid the world of many during the world wars, apart from life hideous as it has been in the Middle East and Asia, there have been no actual world wars. So this is the world war that is a different type of war, All the western governments leaders and their officials are in on the deal. I am sure if you just followed the money and looked at the blind followers of the leftists you would see they are in it for both.

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  3. Are they trying to kill you?

    Short answer: ‘Yes’!

    And if they CAN’T kill you, then they’ll try and organise your lives in such as way that ‘death’ will be seen as being preferable to living.

    Gates et al have a lot to answer for.

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  4. If the vaccine doesn’t kill, the fucking never ending propaganda will drive many over the edge. I have never seen anything like it in my life and I lived in Apartheid South Africa that was full of propaganda. You become sceptical of everything the government says. My basic premise is if Jacinda or Hipkins make a statement, assume the exact opposite is true. Always.

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  5. Vax = cool aid for retards.

    Pppfizer realise the blowback was inevitable. Perhaps this is an internal burnout. A cleaning of the communist house, so to speak. The bodies are building up and the elites will not be able to hide them. Ppppfizer has immunity. Does cinders and the drone Karen’s?

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  6. The Spartacus Letter Part 1 of 2
    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.

    End of Part 1 of 2

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  7. The Letter from Spartacus Part 2 of 2

    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.

    End of Part 2 of 2
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  8. Morning Ed, I know this will go in moderation. I hope you do not mind such long copy & paste to put out these links to back up “The Spartacus Letter”, but the whole package is so important, life & death, and hopefully others will link to share & distribute what they feel is relevant.
    Thank you in advance.
    – – – – – – – – – – – – – – – – –

    The Spartacus Letter -References for Part 1 of 2
    https://www.docdroid.net/kZZXcGS/covid-19-the-spartacus-letter-pdf

    COVID-19 is not a viral pneumonia — it is a viral vascular endotheliitis:

    https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)30937-5/fulltext

    https://academic.oup.com/eurheartj/article/41/32/3038/5901158

    https://www.embopress.org/doi/full/10.15252/embr.202152744

    COVID-19 is not just a respiratory disease — it can precipitate multiple organ failure, including hypoxic and inflammatory damage to various vital organs, such as the brain, heart, liver, pancreas, kidneys, and intestines:

    https://www.nature.com/articles/d41586-021-01693-6https://www.health.harvard.edu/blog/the-hidden-long-term-cognitive-effects-of-covid-2020100821133

    https://www.nature.com/articles/s41422-020-0390-x

    https://www.embopress.org/doi/full/10.15252/embj.2020106230https://jamanetwork.com/journals/jama/fullarticle/2776538

    https://pubmed.ncbi.nlm.nih.gov/32921216/

    https://www.nature.com/articles/s41575-021-00426-4

    https://pubmed.ncbi.nlm.nih.gov/32553666/

    https://www.nature.com/articles/s41467-021-23886-3

    https://pubmed.ncbi.nlm.nih.gov/34081912/

    https://www.nature.com/articles/s41581-021-00452-0
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438210/
    https://www.nature.com/articles/s41598-021-92740-9

    Some of the most common laboratory findings in COVID-19:

    https://www.uptodate.com/contents/covid-19-clinical-features

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426219/

    COVID-19 can present as almost anything:

    https://www.nature.com/articles/s41591-020-0968-3

    https://www.frontiersin.org/articles/10.3389/fmed.2020.00526/full

    COVID-19 is more severe in those with conditions that involve endothelial dysfunction, such as obesity, hypertension, and diabetes:
    https://www.dovepress.com/obesity-related-inflammation-and-endothelial-dysfunction-in-covid-19-i-peer-reviewed-fulltext-article-JIR

    https://jamanetwork.com/journals/jama/fullarticle/2772071https://mdpi-res.com/d_attachment/cells/cells-10-00933/article_deploy/cells-10-00933.pdf

    The vast majority of COVID-19 cases are mild and do not cause significant disease:

    https://www.webmd.com/lung/covid-recovery-overview#1

    https://academic.oup.com/ofid/article/7/9/ofaa286/5875595https://pubmed.ncbi.nlm.nih.gov/33289900/

    In those who have critical COVID-19-induced sepsis, hypoxia, coagulopathy, and ARDS, the most common treatments are intubation, injected corticosteroids, and blood thinners like heparin, which often precipitate harmful hemorrhages:
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7548860/

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448713/https://www.nejm.org/doi/full/10.1056/NEJMoa2103417

    The majority of people who go on a ventilator are dying due to COVID-19 mimicking the physiology of ischemia-reperfusion injury with prolonged transient hypoxia and ischemia, leading directly to the formation of damaging reactive oxygen species:

    https://www.journalofsurgicalresearch.com/article/S0022-4804(14)00176-0/fulltext

    https://www.nature.com/articles/nature13909https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625011/

    https://www.atsjournals.org/doi/full/10.1164/rccm.201401-0168CPhttps://pubmed.ncbi.nlm.nih.gov/18974366/

    The end-stage of COVID-19 is severe lipid peroxidation, where fats in the body start to “rust” due to damage by oxidative stress:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768996/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357498/

    https://www.liebertpub.com/doi/10.1089/ars.2021.0017

    Oxidized lipids appear as foreign objects to the immune system, which recognizes and forms antibodies against OSEs, or oxidation-specific epitopes:

    https://ard.bmj.com/content/annrheumdis/early/2020/08/04/annrheumdis-2020-218145.full.pdf

    https://ard.bmj.com/content/80/9/1236

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7256550/https://www.hss.edu/conditions_top-ten-series-antiphospholipid-syndrome-coronavirus-covid-19.aspIn

    COVID-19, neutrophil degranulation and NETosis in the bloodstream drives severe oxidative damage; hemoglobin becomes incapable of carrying oxygen due to heme iron being stripped out of heme by hypochlorous acid:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757048/

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7436665/

    https://www.nature.com/articles/s41418-021-00805-z

    https://www.sciencedirect.com/science/article/pii/S221249262030052XSARS-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 and blood pressure in the body and in the bloodstream by controlling sodium/potassiumretention and excretion and vascular tone:

    https://www.ncbi.nlm.nih.gov/books/NBK470410/

    https://www.merckmanuals.com/home/multimedia/figure/cvs_regulating_blood_pressure_renin

    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:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7167720/https://www.frontiersin.org/articles/10.3389/fmed.2020.594495/full

    https://www.frontiersin.org/articles/10.3389/fneur.2020.573095/full

    SARS-CoV-2 infects a cell as follows:

    https://www.nature.com/articles/s41401-020-0485-4

    https://www.science.org/doi/10.1126/science.abb2507https://www.sciencedirect.com/science/article/abs/pii/S1931312820306211

    SARS-CoV-2 Spike proteins embedded in a cell can actually cause adjacent human cells to fuse together, forming syncytia/MGCs:

    https://www.nature.com/articles/s41418-021-00782-3https://pubmed.ncbi.nlm.nih.gov/33051876/

    SARS-CoV-2’s viroporins, such as its Envelope protein, act as calcium ion channels, introducing calcium into infected cells:

    https://www.nature.com/articles/s41422-021-00519-4

    https://virologyj.biomedcentral.com/articles/10.1186/s12985-019-1182-0
    The virus suppresses the natural interferon response, resulting in delayed inflammation:

    https://www.nature.com/articles/s12276-021-00592-0https://mdpi-res.com/d_attachment/viruses/viruses-12-01433/article_deploy/viruses-12-01433.pdf

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310780/

    SARS-CoV-2 N protein can also directly activate the NLRP3 inflammasome:

    https://www.nature.com/articles/s41467-021-25015-6

    https://www.frontiersin.org/articles/10.3389/fimmu.2020.01021/full

    SARS-CoV-2 suppresses the Nrf2 antioxidant pathway, reducing the body’s own endogenous antioxidant enzyme activity:

    https://www.nature.com/articles/s41467-020-18764-3

    https://ctajournal.biomedcentral.com/articles/10.1186/s13601-020-00362-7

    https://mdpi-res.com/d_attachment/ijms/ijms-22-07963/article_deploy/ijms-22-07963.pdf

    The suppression of ACE2 by binding with Spike causes a buildup of bradykinin that would otherwise be broken down by ACE2:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7834250/

    https://www.the-scientist.com/news-opinion/is-a -bradykinin-storm-brewing-in-covid-19–67876

    This constant calcium influx into the cells results in (or is accompanied by) noticeable hypocalcemia, or low blood calcium:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292572/

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041474/

    https://www.sciencedirect.com/science/article/abs/pii/S1871402121000059

    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:

    https://www.sciencedirect.com/science/article/abs/pii/S089158490700319X?via%3Dihub

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1218972/https://pubmed.ncbi.nlm.nih.gov/2156053/

    https://www.sciencedirect.com/topics/medicine-and-dentistry/bradykinin-b2-receptor-agonist

    https://www.sciencedirect.com/topics/neuroscience/bradykinin

    NADPH oxidase releases superoxide into the extracellular space:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556774/https://www.pnas.org/content/110/21/8744

    Superoxide radicals react with nitric oxide to form peroxynitrite:

    https://pubmed.ncbi.nlm.nih.gov/8944624/

    https://www.pnas.org/content/115/23/5839

    Peroxynitrite reacts with the tetrahydrobiopterin cofactor needed by endothelial nitric oxide synthase, destroying it and “uncoupling” the eNOS enzymes, causing nitric oxide synthase to synthesize more superoxide instead (this means that every process that upregulates NOS activity now produces superoxide instead of nitric oxide):

    https://pubmed.ncbi.nlm.nih.gov/24353182/https://academic.oup.com/cardiovascres/article/73/1/8/316487

    https://pubs.acs.org/doi/10.1021/bi9016632

    This proceeds in a positive feedback loop until nitric oxide bioavailability in the circulatory system is depleted:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276137/

    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:

    https://journal.chestnet.org/article/S0012-3692(20)34397-X/fulltext

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111989/

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754882/

    The loss of NO allows the virus to begin replicating with impunity in the body (clearly, the virus has an evolutionary incentive to induce oxidative stress to destroy nitric oxide):

    https://scitechdaily.com/nitric-oxide-a-possible-treatment-for-covid-19-only-substance-to-have-a -direct-effect-on-sars-cov-2/

    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:
    https://www.nature.com/articles/s41392-020-00454-7

    https://www.frontiersin.org/articles/10.3389/fphys.2020.605908/full

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430889/https://pubmed.ncbi.nlm.nih.gov/19004510/

    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:

    https://www.frontiersin.org/articles/10.3389/fimmu.2021.652470/full

    https://www.frontiersin.org/articles/10.3389/fimmu.2021.720109/full

    Phagocytic 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:

    https://www.frontiersin.org/articles/10.3389/fimmu.2012.00174/full

    https://jlb.onlinelibrary.wiley.com/doi/full/10.1189/jlb.0809549

    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:

    https://www.sciencedirect.com/topics/neuroscience/superoxide-dismutase

    https://www.sciencedirect.com/topics/medicine-and-dentistry/myeloperoxidase

    In severe and critical COVID-19, there is actually rather severe NETosis:

    https://www.frontiersin.org/articles/10.3389/fphar.2021.708302/full

    https://insight.jci.org/articles/view/138999https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184981/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488868/

    https://ashpublications.org/blood/article/136/10/1169/461219/Neutrophil-extracellular-traps-contribute-to

    https://www.sciencedirect.com/science/article/pii/S221249262030052X

    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:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757048/

    https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0120737

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863623/

    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:

    https://www.sciencedirect.com/science/article/pii/S0753332221000135

    https://sites.kowsarpub.com/ans/articles/60038.html

    https://www.sciencedirect.com/science/article/abs/pii/S0300483X00002316?via%3Dihub

    https://www.sciencedirect.com/topics/chemistry/fenton-reactionhttps://www.researchgate.net/figure/Fenton-and-Haber-Weiss-reactions-are-a -source-of-oxidative-stress-The-generation-of_fig1_330729897

    This condition is not unknown to medical science. The actual name for all of this is acute sepsis (but without the traditional hallmarks of sepsis, like shock):

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056356/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886971/

    https://www.futuremedicine.com/doi/10.2217/fmb-2020-0312https://www.global-sepsis-alliance.org/news/2020/4/7/update-can-covid-19-cause-sepsis-explaining-the-relationship-between-the-coronavirus-disease-and-sepsis-cvd-novel-coronavirus

    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:

    https://onlinelibrary.wiley.com/doi/full/10.1002/ehf2.12958https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264936/

    https://www.sciencedirect.com/science/article/pii/S2213231721001300https://www.researchgate.net/publication/354129433_Preliminary_Findings_on_the_Association_of_the_Lipid_Peroxidation_Product_4-Hydroxynonenal_with_the_Lethal_Outcome_of_Aggressive_COVID-19

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180845/https://rupress.org/jem/article-abstract/218/6/e20210518/212093/Ferroptosis-in-infection-inflammation-and?redirectedFrom=fulltext

    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:

    https://www.nature.com/articles/pr2009174

    The correct treatment for severe COVID-19 related sepsis is non-invasive ventilation, steroids, and antioxidant infusions:
    https://covid19criticalcare.com/covid-19-protocols/math-plus-protocol/

    https://journals.lww.com/ccmjournal/Abstract/2007/09001/Antioxidant_supplementation_in_sepsis_and_systemic.25.aspx

    https://mdpi-res.com/d_attachment/medicina/medicina-56-00619/article_deploy/medicina-56-00619-v2.pdf

    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:

    https://www.hindawi.com/journals/omcl/2018/6581970/

    https://www.intechopen.com/chapters/62672https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708076/https://www.karger.com/Article/Abstract/88623https://www.sciencedirect.com/science/article/abs/pii/000629529390218L?via%3

    DihubIndomethacin prevents iron-driven oxidation of arachidonic acid to isoprostanes:

    https://www.sciencedirect.com/science/article/abs/pii/0161463079900442

    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:

    https://link.springer.com/article/10.1007/s10787-020-00715-5

    Scientists who know anything about pulmonary neutrophilia, ARDS, and redox biology have known or surmised much of this since March 2020:

    https://www.researchgate.net/post/NADPH_oxidase_Covid-19_Oxygen_treatment
    In April 2020, Swiss scientists confirmed that COVID-19 was a systemic vascular endotheliitis:

    https://www.usz.ch/en/covid-19-also-a -systemic-endotheliitis/

    By late 2020, experts had already concluded that COVID-19 causes a form of viral sepsis:

    https://www.healthleadersmedia.com/clinical-care/expert-severe-covid-19-illness-viral-sepsis

    They also know that sepsis can be effectively treated with antioxidants:
    https://jtd.amegroups.com/article/view/34870/htmlhttps://www.evms.edu/about_evms/administrative_offices/marketing_communications/publications/issue_9_4/has-sepsis-met-its-match.php

    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:

    https://ccforum.biomedcentral.com/articles/10.1186/s13054-020-03049-4

    https://jamanetwork.com/journals/jama/fullarticle/2765302

    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 enrolled in these studies, such as Oxford’s ludicrous RECOVERY study, the intervention is too late to have any positive effect (i.e. these RCTs are designed in such a way that the use of antivirals is futile, therefore, these studies are deceptive and unethical by their very nature):

    https://www.mdpi.com/1999-4915/13/6/963/htm

    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:

    https://www.the-hospitalist.org/hospitalist/article/234869/coronavirus-updates/state-inpatient-covid-19-care

    https://www.sciencedirect.com/science/article/pii/S0753332220306867

    It is from this group that the clinical trials for antivirals have recruited, pretty much exclusively (i.e. they do not test prophylaxis/early treatment, only changes to the mean duration of hospitalization for those already hospitalized):

    https://www.nejm.org/doi/full/10.1056/nejmoa2023184https://www.nejm.org/doi/full/10.1056/NEJMoa2022926https://pubmed.ncbi.nlm.nih.gov/34318930/

    India went against the instructions of the WHO and mandated the prophylactic usage of Ivermectin. They have almost completely eradicated COVID-19:

    https://wentworthreport.com/2021/09/11/ivermectin-wins-in-india/https://ivmmeta.com

    The Indian Bar Association of Mumbai has brought criminal charges against WHO Chief Scientist Dr. Soumya Swaminathan for recommending against the use of Ivermectin:

    https://indianbarassociation.in/wp-content/uploads/2021/05/IBA-PRESS-RELEASE-MAY-26-2021.pdf

    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:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043740/

    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, preventingnuclear 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:

    https://www.sciencedirect.com/science/article/abs/pii/S0166354219307211?via%3Dihubhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539925/

    In Bangladesh, Ivermectin costs $1.80 for an entire 5-day course:

    https://journals.lww.com/americantherapeutics/fulltext/2021/08000/ivermectin_for_prevention_and_treatment_of.7.aspx

    Remdesivir, which is toxic to the liver, costs $3,120 for a 5-day course of the drug:

    https://www.npr.org/sections/health-shots/2020/06/29/884648842/remdesivir-priced-at-more-than-3 -100-for-a-course-of-treatmenthttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7386240/

    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:

    https://www.fiercepharma.com/pharma/gilead-s -1 -5b-remdesivir-sales-help-buoy-greater-than-expected-declines-for-mainstay-hiv

    https://www.forbes.com/sites/jvchamary/2021/01/31/remdesivir-covid-coronavirus/?sh=7e6034e666c2

    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:

    https://www.thelancet.com/article/S0140-6736(21)00869-2/fulltext

    https://www.pennmedicine.org/updates/blogs/penn-physician-blog/2020/august/airborne-droplet-debate-article

    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:

    https://www.nature.com/articles/d41586-021-00251-4

    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:

    https://www.medrxiv.org/content/10.1101/2020.08.03.20167395v1https://khn.org/news/fact-check-airborne-transmission-coronavirus-science-behind-aerosol-spread/

    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:

    https://ajicjournal.org/retrieve/pii/S0196655305801439

    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 (in a pinch, surgical masks can be modified or worn a specific way to increase filtration):

    https://www.epa.gov/sciencematters/epa-researchers-test-effectiveness-face-masks-disinfection-methods-against-covid-19https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409952/https://www.mopec.com/coronavirus-protection-made-easy-with-the-maxair-capr/

    Live SARS-CoV-2 may potentially be detected in sewage outflows, and there may be oral-fecal transmission:

    https://www.sciencedirect.com/science/article/pii/S0048969720325936https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0249568https://www.nature.com/articles/s41587-020-0684-z

    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 (there is some valid concern that COVID-19 may also spread the same way, given its similarities to SARS):

    https://pubmed.ncbi.nlm.nih.gov/16696450/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC539564/https://www.neha.org/sites/default/files/jeh/JEH5.06-Feature-Environmental-Transmission-of-SARS.pdf

    https://www.cleanlink.com/news/article/COVID-19-Could-Spread-Through-Dry-Floor-Drains–25600

    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:

    https://www.healthline.com/health-news/leaky-vaccines-can-produce-stronger-versions-of-viruses-072715

    https://www.realclearscience.com/articles/2021/08/23/lets_stop_pretending_about_the_covid-19_vaccines_791050.html

    https://www.cdc.gov/media/releases/2021/s0730-mmwr-covid-19.htmlhttps://www.businessinsider.com/cdc-fully-vaccinated-new-guidelines-wear-masks-indoors-delta-2021-7?utm_source=yahoo.com&utm_medium=referral

    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:

    https://www.jdsupra.com/legalnews/accelerated-c ovid-19-vaccine-clinical-95853/

    https://www.nebraskamed.com/COVID/were-the-covid-19-vaccines-rushed

    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:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439223/https://cen.acs.org/pharmaceuticals/drug-delivery/Without-lipid-shells-mRNA-vaccines/99/i8

    https://www.cdc.gov/coronavirus/2019-ncov/vaccines/different-vaccines/mrna.html

    https://medlineplus.gov/genetics/understanding/therapy/mrnavaccines/

    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:

    https://www.nature.com/articles/s41586-020-2622-0

    https://coronavirus.dc.gov/sites/default/files/dc/sites/coronavirus/page_content/attachments/Cartoon%20Explainer%20How%20the%20Moderna%20and%20Pfizer%20Vaccines%20Work.pdf

    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:

    https://www.health.nd.gov/sites/www/files/documents/COVID%20Vaccine%20Page/COVID-19_Vaccine_Fetal_Cell_Handout.pdfhttps://cmda.org/the-ethics-of-the-sars-cov-2 -vaccines-revisited/

    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:

    https://mcusercontent.com/22e41db63deaf4a84be439c0f/files/6a33980b-683f-4ee4-67d4-cc98dc7fcd37/20210601_Guide_to_COVID_19_vaccines_for_parents.pdf

    https://rightsfreedoms.wordpress.com/2021/06/16/researcher-we-made-a-big-mistake-on-covid-19-vaccine/

    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:

    https://www.nature.com/articles/s41467-020-20321-x

    https://cen.acs.org/pharmaceuticals/vaccines/tiny-t weak-behind-COVID-19/98/i38

    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:

    https://files.catbox.moe/0vwcmj.pdfThese lipid nanoparticles may trigger anaphylaxis in an unlucky few:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441754/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862013/

    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:

    https://elifesciences.org/articles/61984https://www.frontiersin.org/articles/10.3389/fgene.2018.00431/full

    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:

    https://academic.oup.com/cid/advance-article/doi/10.1093/cid/ciab465/6279075

    https://www.nature.com/articles/s41564-021-00908-whttps://www.life-science-alliance.org/content/3/9/e202000786

    SARS-CoV-2 Spike has a Superantigenic region (SAg), which may promote extreme inflammation:

    https://www.pnas.org/content/117/41/25254https://www.nature.com/articles/s41577-021-00502-5

    Anti-Spike antibodies were found in one study to function as autoantibodies and attack the body’s own cells:

    https://www.researchsquare.com/article/rs-612103/v2

    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:

    https://drrichswier.com/2021/09/18/summary-covid-19-vaccine-concerns/https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-july-13-2021

    https://www.medpagetoday.com/infectiousdisease/covid19vaccine/94061?xid=nl_mpt_DHE_2021-08-17

    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:

    https://www.nature.com/articles/s41564-021-00958-0

    https://www.mdpi.com/1422-0067/22/3/992/pdf

    https://pubs.acs.org/doi/10.1021/acschemneuro.0c00619https://www.science.org/doi/full/10.1126/science.abd3072https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0253347

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7799037/

    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:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827936/

    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:

    https://journals.asm.org/doi/full/10.1128/JVI.01751-20https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457603/

    https://yurideigin.medium.com/lab-made-cov2-genealogy-through-the-lens-of-gain-of-function-research-f96dd7413748

    SARS-CoV-2 Spike has a prion-like domain that enhances its infectiousness:

    https://www.preprints.org/manuscript/202003.0422/v1

    https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0023664

    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:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988450/

    This is very concerning because SARS-CoV-2 S1 is capable of penetrating the blood-brain barrier and entering the brain.
    It is capable of increasing the permeability of the blood-brain barrier to itself and other molecules by injuring and disrupting it directly:

    https://www.nature.com/articles/s41593-020-00771-8

    https://www.nature.com/articles/s41392-021-00719-9

    https://pubmed.ncbi.nlm.nih.gov/33053430/

    SARS-CoV-2, like other betacoronaviruses, may have Dengue-like ADE, or antibody-dependent enhancement of disease:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943455/

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7454712/https://www.journalofinfection.com/article/S0163-4453(21)00392-3/fulltext

    https://sharylattkisson.com/2021/08/study-why-so-many-vaccinated-people-are-getting-sick/https://www.nature.com/articles/s41564-020-00789-5

    https://www.sciencedirect.com/science/article/pii/S1201971220307311

    https://pubmed.ncbi.nlm.nih.gov/31826992/

    https://www.biorxiv.org/content/10.1101/2021.08.22.457114v1

    There is 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:

    https://www.jimmunol.org/content/202/2/335https://en.wikipedia.org/wiki/Original_antigenic_sin

    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:

    https://en.wikipedia.org/wiki/Antibody-dependent_enhancement

    https://www.cdc.gov/dengue/training/cme/ccm/page57857.html

    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-naïve:

    https://www.frontiersin.org/articles/10.3389/fcimb.2020.572681/fullhttps://news.unchealthcare.org/2021/06/scientists-discover-how-dengue-vaccine-fails-to-protect-against-disease/

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739535/

    https://www.scientificamerican.com/article/how-the-worlds-first-dengue-vaccination-drive-ended-in-disaster/

    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:

    https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0035421

    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:

    https://pubmed.ncbi.nlm.nih.gov/33330870/

    https://rightsfreedoms.wordpress.com/2021/08/13/mit-harvard-study-suggests-mrna-vaccine-might-permanently-alter-dna-after-all/

    https://home.solari.com/deep-state-tactics-101-the-covid-injection-fraud-its-not-a -vaccine/

    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:

    https://www.phe.gov/s3/dualuse/documents/gain-of-function.pdf

    https://www.scientificamerican.com/article/u-s -lifts-moratorium-on-funding-controversial-high-risk-virus-research/

    https://www.nih.gov/about-nih/who-we-are/nih-director/statements/nih-lifts-funding-pause-gain-function-research

    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:

    https://sph.unc.edu/adv_profile/ralph-s-baric-phd/https://alumni.unc.edu/news/ralph-baric-on-the-front-lines-of-coronavirus-for-three-decades/

    Ralph Baric and Shi Zhengli are colleagues and have co-written papers together:

    https://www.nature.com/articles/nm.3985/

    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

    https://www.technologyreview.com/2021/06/29/1027290/gain-of-function-risky-bat-virus-engineering-links-america-to-wuhan/

    https://usrtk.org/biohazards-blog/ralph-baric-emails/https://www.paul.senate.gov/newsweek-op-ed-congress-must-pursue-answers-about-origin-covid-19

    https://nymag.com/intelligencer/article/coronavirus-lab-escape-theory.html

    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:

    https://peterdaszak.com/https://peterdaszak.com/interceptdocs.pdfhttps://theintercept.com/2021/09/09/covid-origins-gain-of-function-research/https://nationalfile.com/bombshell-fauci-kept-funding-peter-daszaks-wuhan-gain-of-function-experiments-with-7 -5 -million-after-trump-canceled-grant/

    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:

    https://www.independentsciencenews.org/wp-content/uploads/2020/12/EcoHealth-Funding-as-of-01_10_2020-Fed.-Grants-Contracts.pdf

    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:

    https://www.algora.com/Algora_blog/2021/09/22/ecohealth-alliance-darpa-toyed-with-infecting-wild-chinese-bats-with-covid-leaked-docs-allege

    https://nypost.com/2021/07/01/pentagon-gave-millions-to-ecohealth-alliance-for-wuhan-lab/

    https://www.judicialwatch.org/press-releases/wuhan-lab-fauci-grants/

    https://www.judicialwatch.org/documents/jw-v -nih-wuhan-june-2021-00696/

    https://scholar.harvard.edu/files/kleelerner/files/20200414_wapo_-_state_department_cables_warned_of_safety_issues_at_wuhan_lab_studying_bat_coronaviruses_-_the_washington_post.pdf

    https://www.businessinsider.com/us-officials-raised-alarms-about-safety-issues-in-wuhan-lab-report-2020-4?op=1

    Chinese scientists in Wuhan reported being routinely bitten and urinated on by laboratory animals:
    https://img-prod.tgcom24.mediaset.it/images/2020/02/16/114720192-5eb8307f-017c-4075-a697-348628da0204.pdf

    https://web.archive.org/web/20200214144447/

    https:/www.researchgate.net/publication/339070128_The_possible_origins_of_2019-nCoV_coronavirusIn

    November of 2019, three technicians at the Wuhan Institute of Virology developed symptoms consistent with a flu-like illness:

    https://www.webmd.com/lung/news/20210524/wuhan-lab-researchers-illness

    https://thehill.com/policy/healthcare/556815-fauci-calls-on-china-to-release-medical-records-of-wuhan-researchers

    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:

    https://rightsfreedoms.wordpress.com/2021/06/26/confidential-documents-reveal-moderna-sent-mrna-coronavirus-vaccine-candidate-to-university-researchers-weeks-before-emergence-of-covid-19/

    https://s3.documentcloud.org/documents/6935295/NIH-Moderna-Confidential-Agreements.pdf

    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 :

    https://www.cidrap.umn.edu/news-perspective/2020/01/china-releases-genetic-data-new-coronavirus-now-deadly

    https://www.sciencedaily.com/releases/2020/01/200131114748.htm

    Moderna claims, rather absurdly, that they developed a working vaccine from this sequence in under 48 hours:

    https://www.businessinsider.com/moderna-designed-coronavirus-vaccine-in-2-days-2020-11https://globalnews.ca/news/7492076/moderna-coronavirus-vaccine-technology-how-it -works/

    https://nymag.com/intelligencer/2020/12/moderna-covid-19-vaccine-design.html

    Stéphane Bancel, the current CEO of Moderna, was formerly the CEO of bioMérieux, a French multinational corporation specializing in medical diagnostic tech, founded by one Alain Mérieux:

    https://www.biomerieux.com/en/board-directors-biomerieux-chaired-alain-merieux-has-appointed-stephane-bancel-directeur-generalhttps://en.wikipedia.org/wiki/St%C3%A9phane_Bancelhttps://www.himss.org/global-conference/speaker-stephane-bancel

    Alain Mérieux was one of the individuals who was instrumental in the construction of the Wuhan Institute of Virology’s P4 lab:

    https://www.fondation-merieux.org/en/news/alain-merieux-receives-the-prestigious-chinese-reform-friendship-award/https://medicalxpress.com/news/2020-04-wuhan-lab-core-virus-controversy.html

    http://english.whiov.cas.cn/ne/201712/t20171212_187624.html

    https://web.archive.org/web/20210921133410/

    http://english.whiov.cas.cn/ne/201712/t20171212_187624.html

    The sequence given as the closest relative to SARS-CoV-2, RaTG13, is not a real virus.
    It is a forgery:

    https://nerdhaspower.weebly.com/ratg13-is-fake.html

    https://gnews.org/192144/

    https://www.peakprosperity.com/forum-topic/scientific-history-of-ratg13/

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

    https://www.technologyreview.com/2021/03/26/1021263/bat-covid-coronavirus-cause-origin-wuhan/https://www.who.int/news-room/feature-stories/detail/how-who-is-working-to-track-down-the-animal-reservoir-of-the-sars-cov-2 -virus

    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:

    https://www.freep.com/story/news/local/michigan/macomb/2020/04/28/allure-medical-spa-shelby-covid-vitamin-c/3038801001/

    https://www.detroitnews.com/story/news/local/macomb-county/2020/05/15/doctor-got-loan-while-peddling-phony-covid-19-cure-feds-say/5197315002/

    https://covid19criticalcare.com/covid-19-protocols/math-plus-protocol/

    https://covid19criticalcare.com/wp-content/uploads/2021/01/FLCCC-Alliance-MATHplus-Protocol-ENGLISH.pdfhttps://pubmed.ncbi.nlm.nih.gov/31978969/

    https://www.sciencedirect.com/science/article/abs/pii/S0883944119316107?via%3Dihub

    https://www.npr.org/sections/health-shots/2019/10/01/766029397/mixed-results-for-a-test-of-vitamin-c-for-sepsis

    https://www.nutraingredients.com/Article/2020/01/28/Ethically-and-morally-unacceptable-Reaction-to-vitamin-C-for-sepsis-trial

    The FDA banned ranitidine (Zantac) due to supposed NDMA (N-nitrosodimethylamine) contamination :

    https://www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press-announcements-ndma-zantac-ranitidine

    https://www.raps.org/news-and-articles/news-articles/2021/6/fda-studies-no-post-ingestion-ndma-from-ranitidine

    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:

    https://onlinelibrary.wiley.com/doi/10.1111/j.1472-8206.2009.00810.x

    https://www.sciencedirect.com/science/article/pii/S1347861319342203

    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:

    https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/les-labs-593764-07232020https://www.naturalproductsinsider.com/regulatory/us-senator-npa-press-fda-nac-supplements

    https://www.nutraingredients-usa.com/Article/2021/05/11/CRN-This-is-not-the-final-word-on-NAC

    https://www.naturalproductsinsider.com/regulatory/amazon-confirms-plans-removing-nac-supplements

    On June 9th, 2020, Charles Lieber, a Harvard nanotechnology researcher with decades of experience, was indicted by the DOJ for fraud:

    https://www.justice.gov/opa/pr/harvard-university-professor-and-two-chinese-nationals-charged-three-separate-china-related

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