Latest posts of: eddie13

So I saw this "Spartacus Letter" a while ago and then I saw it here on this board..
I started reading it here and then the thread with it included here in P&S was deleted..
Then I went to find it elsewhere on the net to read and wow, its been deleted almost everywhere across the net too, even archive.is won't load it..

But I found it Wink

So here I am posting it to this board again..
I'm not finished reading it yet but m finding it highly intelligent and worth some of my time so will probably finish reading it..

I haven't read quite enough of it yet to comment too much along with it but this should be enough commenting for YOU NOT TO DELEAT IT!!
So don't delete it..

Oh BTW haha imma post it all including source links..

https://files.catbox.moe/lmpfbp.pdf
Reposted by Anonymous, thanks guy.. But who knows how long that link will last..

Quote

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-CoV2 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-CoV2’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 HaberWeiss 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 irondriven 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 dropletborne. 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 SARSCoV-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 newlyencountered 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-naïve.
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.
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. Alain
Mérieux 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 wellestablished.
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 Stéphane
Bancel, and their accomplices, would have been indicted and prosecuted to the fullest extent of the law.
Instead, billions of our tax dollars were awarded to the perpetrators.
The FBI raided Allure Medical in Shelby Township north of Detroit for billing insurance for “fraudulent
COVID-19 cures”. The treatment they were using? Intravenous Vitamin C. An antioxidant. Which, as
described above, is an entirely valid treatment for COVID-19-induced sepsis, and indeed, is now part of
the MATH+ protocol advanced by Dr. Paul E. Marik.
The FDA banned ranitidine (Zantac) due to supposed NDMA (N-nitrosodimethylamine) contamination.
Ranitidine is not only an H2 blocker used as antacid, but also has a powerful antioxidant effect,
scavenging hydroxyl radicals. This gives it utility in treating COVID-19.
The FDA also attempted to take N-acetylcysteine, a harmless amino acid supplement and antioxidant,
off the shelves, compelling Amazon to remove it from their online storefront.
This leaves us with a chilling question: did the FDA knowingly suppress antioxidants useful for treating
COVID-19 sepsis as part of a criminal conspiracy against the American public?
The establishment is cooperating with, and facilitating, the worst criminals in human history, and are
actively suppressing non-vaccine treatments and therapies in order to compel us to inject these
criminals’ products into our bodies. This is absolutely unacceptable.
COVID-19 Vaccine Development and Links to Transhumanism:
This section deals with some more speculative aspects of the pandemic and the medical and scientific
establishment’s reaction to it, as well as the disturbing links between scientists involved in vaccine
research and scientists whose work involved merging nanotechnology with living cells.
On June 9th, 2020, Charles Lieber, a Harvard nanotechnology researcher with decades of experience, was
indicted by the DOJ for fraud. Charles Lieber received millions of dollars in grant money from the US
Department of Defense, specifically the military think tanks DARPA, AFOSR, and ONR, as well as NIH and
MITRE. His specialty is the use of silicon nanowires in lieu of patch clamp electrodes to monitor and
modulate intracellular activity, something he has been working on at Harvard for the past twenty years.
He was claimed to have been working on silicon nanowire batteries in China, but none of his colleagues
can recall him ever having worked on battery technology in his life; all of his research deals with
bionanotechnology, or the blending of nanotech with living cells.
The indictment was over his collaboration with the Wuhan University of Technology. He had doubledipped, 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 technocraticsocialist “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.

p.s. do not delete