patrick.net

(text copied out of the pdf)

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 02.

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 02 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 02. It's a catch-22, because we need
oxygen to make Adenosine Triphosphate (that is, to live), but 02 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. 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-nai 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 12,
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 11, 2020, that China allegedly
sent us the sequence to what would become known as SARS-CoV-2. Moderna claims,
rather absurdly, that they developed a working vaccine from this sequence in
under 48 hours.

Stephane Bancel, the current CEO of Moderna, was formerly the CEO of bioMerieux,
a French multinational corporation specializing in medical diagnostic tech,
founded by one Alain Merieux. Alain Merieux was one of the individuals who was
instrumental in the construction of the Wuhan Institute of Virology's P4 lab.

The sequence given as the closest relative to SARS-CoV-2, RaTG13, is not a real
virus. It is a forgery. It was made by entering a gene sequence by hand into a
database, to create a cover story for the existence of SARS-CoV-2, which is very
likely a gain-of-function chimera produced at the Wuhan Institute of Virology
and was either leaked by accident or intentionally released. The animal
reservoir of SARS-CoV-2 has never been found.

This is not a conspiracy theory. It is an actual criminal conspiracy, in which
people connected to the development of Moderna's mRNA-1273 are directly
connected to the Wuhan Institute of Virology and their gain-of-function research
by very few degrees of separation, if any. The paper trail is well-established.

The lab-leak theory has been suppressed because pulling that thread leads one to
inevitably conclude that there is enough circumstantial evidence to link
Moderna, the NIH, the WIV, and both the vaccine and the virus's creation
together. In a sane country, this would have immediately led to the world's
biggest RICO and mass murder case. Anthony Fauci, Peter Daszak, Ralph Baric, Shi
Zhengli, and Stephane Bancel, and their accomplices, would have been indicted
and prosecuted to the fullest extent of the law. Instead, billions of our tax
dollars were awarded to the perpetrators.

The FBI raided Allure Medical in Shelby Township north of Detroit for billing
insurance for "fraudulent COVID-19 cures". The treatment they were using?
Intravenous Vitamin C. An antioxidant. Which, as described above, is an entirely
valid treatment for COVID-19-induced sepsis, and indeed, is now part of the
MATH+ protocol advanced by Dr. Paul E. Marik.

The FDA banned ranitidine (Zantac) due to supposed NDMA (N-nitrosodimethylamine)
contamination. Ranitidine is not only an H2 blocker used as antacid, but also
has a powerful antioxidant effect, scavenging hydroxyl radicals. This gives it
utility in treating COVID-19.

The FDA also attempted to take N-acetylcysteine, a harmless amino acid
supplement and antioxidant, off the shelves, compelling Amazon to remove it from
their online storefront.

This leaves us with a chilling question: did the FDA knowingly suppress
antioxidants useful for treating COVID-19 sepsis as part of a criminal
conspiracy against the American public? The establishment is cooperating with,
and facilitating, the worst criminals in human history, and are actively
suppressing non-vaccine treatments and therapies in order to compel us to inject
these criminals' products into our bodies. This is absolutely unacceptable.

COVID-19 Vaccine Development and Links to Transhumanism:

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

On June 9, 2020, Charles Lieber, a Harvard nanotechnology researcher with
decades of experience, was indicted by the DOJ for fraud. Charles Lieber
received millions of dollars in 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 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-MaIthusians 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.

(transcribed into plain text from the pdf, which may have malware embedded)

The references are in the comment below.