A Summary Indictment of the Global RAPE We're Being Subjected To
https://archives.simplelists.com/nfu/cache/17755832/2.pdf
by Spartacus
or
https://www.simplelists.com/nfu/cache/17755832/2.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 O2.
The breakdown of the pathology is as
follows:
SARS-CoV-2 Spike binds to ACE2. Angiotensin Converting Enzyme 2 is an enzyme that is part
of the renin-angiotensin-aldosterone system, or RAAS.
The RAAS is a hormone control system that moderates fluid volume in the body
and in the bloodstream (i.e. osmolarity) by
controlling salt retention and excretion. This protein, ACE2, is ubiquitous in
every part of the body that interfaces with the circulatory system,
particularly in vascular endothelial cells and pericytes,
brain astrocytes, renal tubules and podocytes, pancreatic islet cells, bile duct and intestinal
epithelial cells, and the seminiferous ducts of the
testis, all of which SARS-CoV-2 can infect, not just the lungs.
SARS-CoV-2 infects a cell as follows: SARS-CoV-2 Spike undergoes a
conformational change where the S1 trimers flip up
and extend, locking onto ACE2 bound to the surface of a cell. TMPRSS2, or transmembrane protease serine 2, comes along and cuts off
the heads of the Spike, exposing the S2 stalk-shaped subunit inside. The
remainder of the Spike undergoes a conformational change that causes it to
unfold like an extension ladder, embedding itself in the cell membrane. Then,
it folds back upon itself, pulling the viral membrane and the cell membrane
together. The two membranes fuse, with the virus’s proteins migrating out onto
the surface of the cell. The SARS-CoV-2 nucleocapsid
enters the cell, disgorging its genetic material and beginning the viral
replication process, hijacking the cell’s own structures to produce more virus.
SARS-CoV-2 Spike proteins embedded in a cell can actually cause human cells to
fuse together, forming syncytia/MGCs (multinuclear
giant cells). They also have other pathogenic, harmful effects. SARS-CoV-2’s viroporins, such as its Envelope protein, act as calcium
ion channels, introducing calcium into infected cells. The virus suppresses the
natural interferon response, resulting in delayed inflammation. SARS-CoV-2 N
protein can also directly activate the NLRP3 inflammasome.
Also, it suppresses the Nrf2 antioxidant pathway. The suppression of ACE2 by
binding with Spike causes a buildup of bradykinin
that would otherwise be broken down by ACE2.
This constant calcium influx into the cells results in (or is accompanied by)
noticeable hypocalcemia, or low blood calcium,
especially in people with Vitamin D deficiencies and pre-existing endothelial dysfunction.
Bradykinin upregulates cAMP, cGMP, COX, and Phospholipase C activity. This results in prostaglandin
release and vastly increased intracellular calcium signaling, which promotes
highly aggressive ROS release and ATP depletion. NADPH oxidase
releases superoxide into the extracellular space. Superoxide radicals react
with nitric oxide to form peroxynitrite. Peroxynitrite reacts with the tetrahydrobiopterin
cofactor needed by endothelial nitric oxide synthase,
destroying it and “uncoupling” the enzymes, causing nitric oxide synthase to synthesize more superoxide instead. This
proceeds in a positive feedback loop until nitric oxide bioavailability in the
circulatory system is depleted.
Dissolved nitric oxide gas produced constantly by eNOS
serves many important functions, but it is also antiviral against SARS-like coronaviruses, preventing the palmitoylation
of the viral Spike protein and making it harder for it to bind to host
receptors. The loss of NO allows the virus to begin replicating with impunity
in the body. Those with endothelial dysfunction (i.e. hypertension, diabetes,
obesity, old age,
African-American race) have redox equilibrium issues
to begin with, giving the virus an advantage.
Due to the extreme cytokine release triggered by these processes, the body summons a great deal of neutrophils
and monocyte-derived alveolar macrophages to the
lungs.
Cells of the innate immune system
are the first-line defenders against pathogens. They work by engulfing invaders
and trying to attack them with enzymes that produce powerful oxidants, like SOD
and MPO. Superoxide dismutase takes superoxide and makes hydrogen peroxide, and
myeloperoxidase takes hydrogen peroxide and chlorine
ions and makes hypochlorous acid, which is many, many
times more reactive than sodium hypochlorite bleach.
Neutrophils have a nasty trick. They can also eject
these enzymes into the extracellular space, where they will continuously spit
out peroxide and bleach into the bloodstream. This is called neutrophil extracellular trap formation, or, when it
becomes pathogenic and counterproductive, NETosis. In
severe and critical COVID-19, there is actually rather severe NETosis.
Hypochlorous acid building up in the bloodstream
begins to bleach the iron out of heme and compete for
O2 binding sites. Red blood cells lose the ability to transport oxygen, causing
the sufferer to turn blue in the face. Unliganded
iron, hydrogen peroxide, and superoxide in the bloodstream undergo the
Haber-Weiss and Fenton reactions, producing extremely reactive hydroxyl radicals
that violently strip electrons from surrounding fats and DNA, oxidizing them
severely.
This condition is not unknown to medical science. The actual name for all of
this is acute sepsis. We know this is happening in COVID-19 because people who have
died of the disease have noticeable ferroptosis
signatures in their tissues, as well as various other oxidative stress markers
such as nitrotyrosine, 4-HNE, and malondialdehyde.
When you intubate someone with this condition, you
are setting off a free radical bomb by supplying the cells with O2. It’s a
catch-22, because we need oxygen to make Adenosine Triphosphate
(that is, to live), but O2 is also the precursor of all these damaging radicals
that lead to lipid peroxidation.
The correct treatment for severe COVID-19 related sepsis is non-invasive
ventilation, steroids, and antioxidant infusions. Most of the drugs repurposed
for COVID-19 that show any benefit whatsoever in rescuing critically-ill
COVID-19 patients are antioxidants. N-acetylcysteine,
melatonin, fluvoxamine, budesonide,
famotidine, cimetidine, and
ranitidine are all antioxidants. Indomethacin
prevents iron-driven oxidation of arachidonic acid to
isoprostanes. There are powerful antioxidants such as
apocynin that have not even been tested on COVID-19
patients yet which could defang neutrophils, prevent
lipid peroxidation, restore endothelial health, and
restore oxygenation to the tissues.
Scientists who know anything about
pulmonary neutrophilia, ARDS, and redox
biology have known or surmised much of this since March 2020. In April 2020,
Swiss scientists confirmed that COVID-19 was a vascular endotheliitis.
By late 2020, experts had already concluded that COVID-19 causes a form of
viral sepsis. They also know that sepsis can be effectively treated with
antioxidants. None of this information is particularly new, and yet, for the
most part, it has not been acted upon. Doctors continue to use damaging
intubation techniques with high PEEP settings despite high lung compliance and
poor oxygenation, killing an untold number of critically ill patients with
medical malpractice.
Because of the way they are constructed, Randomized Control Trials will never
show any benefit for anyantiviral against COVID-19.
Not Remdesivir, not Kaletra,
not HCQ, and not Ivermectin. The reason for this is
simple; for the patients that they have recruited for these studies, such as
Oxford’s ludicrous RECOVERY study, the intervention is too late to have any
positive effect.
The clinical course of COVID-19 is such that by the time most people seek
medical attention for hypoxia, their viral load has
already tapered off to almost nothing. If someone is about 10 days
post-exposure and has already been symptomatic for five days, there is hardly
any virus left in their bodies, only cellular damage and derangement that has
initiated a hyperinflammatory response. It is from
this group that the clinical trials for antivirals
have recruited, pretty much exclusively.
In these trials, they give antivirals to severely ill
patients who have no virus in their bodies, only a delayed hyperinflammatory
response, and then absurdly claim that antivirals
have no utility in treating or preventing COVID-19. These clinical trials do
not recruit people who are pre-symptomatic. They do not test pre-exposure or
post-exposure prophylaxis.This is like using a
defibrillator to shock only flatline, and then
absurdly claiming that defibrillators have no medical utility whatsoever when
the patients refuse to rise from the dead. The intervention is too late. These
trials for antivirals show systematic, egregious
selection bias. They are providing a treatment that is futile to the specific
cohort they are enrolling.
India went against the instructions of the WHO and mandated the prophylactic
usage of Ivermectin. They have almost completely
eradicated COVID-19. The Indian Bar Association of Mumbai has brought criminal
charges against WHO Chief Scientist Dr. Soumya Swaminathan for recommending against the use of Ivermectin.
Ivermectin is not “horse dewormer”.
Yes, it is sold in veterinary paste form as a dewormer
for animals. It has also been available in pill form for humans for decades, as
an antiparasitic drug.
The media have disingenuously claimed that because Ivermectin
is an antiparasitic drug, it has no utility as an
antivirus. This is incorrect. Ivermectin has utility
as an antiviral. It blocks importin, preventing nuclear
import, effectively inhibiting viral access to cell nuclei. Many drugs
currently on the market have multiple modes of action. Ivermectin
is one such drug. It is both antiparasitic and
antiviral.
In Bangladesh, Ivermectin costs $1.80 for an entire
5-day course. Remdesivir, which is toxic to the
liver, costs $3,120 for a 5-day course of the drug. Billions of dollars of
utterly useless Remdesivir were sold to our
governments on the taxpayer’s dime, and it ended up being totally useless for
treating hyperinflammatory COVID-19. The media has
hardly even covered this at all.
The opposition to the use of generic
Ivermectin is not based in science. It is purely
financially and politically-motivated. An effective non-vaccine intervention
would jeopardize the rushed FDA approval of patented vaccines and medicines for
which the pharmaceutical industry stands to rake in billions upon billions of
dollars in sales on an ongoing basis.
The majority of the public are scientifically
illiterate and cannot grasp what any of this even means, thanks to a pathetic
educational system that has miseducated them. You
would be lucky to find 1 in 100 people who have even the faintest clue what any
of this actually means.
COVID-19 Transmission:
COVID-19 is airborne. The WHO carried water for China by claiming that the
virus was only droplet-borne. Our own CDC absurdly claimed that it was mostly
transmitted by fomite-to-face contact, which, given
its rapid spread from Wuhan to the rest of the world, would have been
physically impossible.
The ridiculous belief in fomite-to-face being a
primary mode of transmission led to the use of surface disinfection protocols
that wasted time, energy, productivity, and disinfectant.
The 6-foot guidelines are absolutely useless. The minimum safe distance to
protect oneself from an aerosolized virus is to be 15+ feet away from an
infected person, no closer. Realistically, no public transit
is safe.
Surgical masks do not protect you from aerosols. The virus is too small and the
filter media has too large of gaps to filter it out. They may catch respiratory
droplets and keep the virus from being expelled by someone who is sick, but
they do not filter a cloud of infectious aerosols if someone were to walk into said
cloud.
The minimum level of protection against this virus is quite literally a P100
respirator, a PAPR/CAPR, or a 40mm NATO CBRN respirator, ideally paired with a
full-body tyvek or tychem
suit, gloves, and booties, with all the holes and gaps taped.
Live SARS-CoV-2 may potentially be detected in sewage outflows, and there may
be oral-fecal transmission. During the SARS outbreak in 2003, in the Amoy
Gardens incident, hundreds of people were infected by aerosolized fecal matter
rising from floor drains in their apartments.
COVID-19 Vaccine Dangers:
The vaccines for COVID-19 are not sterilizing and do not prevent infection or
transmission. They are “leaky” vaccines. This means they remove the
evolutionary pressure on the virus to become less lethal. It also means that
the vaccinated are perfect carriers. In other words, those who are vaccinated
are a threat to the unvaccinated, not the other way around.
All of the COVID-19 vaccines currently in use have undergone minimal testing,
with highly accelerated clinical trials. Though they appear to limit severe
illness, the long-term safety profile of these vaccines remains unknown.
Some of these so-called “vaccines” utilize an untested new technology that has
never been used in vaccines before. Traditional vaccines use weakened or killed
virus to stimulate an immune response. The Moderna
and Pfizer-BioNTech vaccines do not. They are
purported to consist of an intramuscular shot containing a suspension of lipid nanoparticles filled with messenger RNA. The way they
generate an immune response is by fusing with cells in a vaccine recipient’s
shoulder, undergoing endocytosis, releasing their
mRNA cargo into those cells, and then utilizing the ribosomes
in those cells to synthesize modified SARS-CoV-2 Spike proteins in-situ.
These modified Spike proteins then migrate to the surface of the cell, where
they are anchored in place by a transmembrane domain.
The adaptive immune system detects the non-human viral protein being expressed
by these cells, and then forms antibodies against that protein. This is
purported to confer protection against the virus, by training the adaptive
immune system to recognize and produce antibodies against the Spike on the
actual virus. The J&J and AstraZeneca vaccines do something similar, but
use an adenovirus vector for genetic material delivery instead of a lipid nanoparticle. These vaccines were produced or validated
with the aid of fetal cell lines HEK-293 and PER.C6, which people with certain
religious convictions may object strongly to.
SARS-CoV-2 Spike is a highly pathogenic protein on its own. It is impossible to
overstate the danger presented by introducing this protein into the human body.
It is claimed by vaccine manufacturers that the vaccine remains in cells in the
shoulder, and that SARS-CoV-2 Spike produced and expressed by these cells from
the vaccine’s genetic material is harmless and inert, thanks to the insertion
of prolines in the Spike sequence to stabilize it in
the prefusion conformation, preventing the Spike from
becoming active and fusing with other cells. However, a pharmacokinetic study
from Japan showed that the lipid nanoparticles and
mRNA from the Pfizer vaccine did not stay in the shoulder, and in fact bioaccumulated in many different organs, including the reproductive
organs and adrenal glands, meaning that modified Spike is being expressed quite
literally all over the place. These lipid nanoparticles
may trigger anaphylaxis in an unlucky few, but far more concerning is the unregulated
expression of Spike in various somatic cell lines far from the injection site and
the unknown consequences of that.
Messenger RNA is normally consumed right after it is produced in the body,
being translated into a protein by a ribosome. COVID-19 vaccine mRNA is
produced outside the body, long before a ribosome translates it. In the
meantime, it could accumulate damage if inadequately preserved. When a ribosome
attempts to translate a damaged strand of mRNA, it can become stalled. When
this happens, the ribosome becomes useless for translating proteins because it
now has a piece of mRNA stuck in it, like a lace card in an old punch card
reader. The whole thing has to be cleaned up and new ribosomes
synthesized to replace it. In cells with low ribosome turnover, like nerve
cells, this can lead to reduced protein synthesis, cytopathic
effects, and neuropathies.
Certain proteins, including SARS-CoV-2 Spike, have proteolytic
cleavage sites that are basically like little dotted lines that say “cut here”,
which attract a living organism’s own proteases (essentially, molecular scissors)
to cut them. There is a possibility that S1 may be proteolytically
cleaved from S2, causing active S1 to float away into the bloodstream while
leaving the S2 “stalk” embedded in the membrane of the cell that expressed the
protein.
SARS-CoV-2 Spike has a Superantigenic region (SAg), which may promote extreme inflammation.
Anti-Spike antibodies were found in one study to function as autoantibodies and attack the body’s own cells. Those who
have been immunized with COVID-19 vaccines have developed blood clots, myocarditis, Guillain-Barre
Syndrome, Bell’s Palsy, and multiple sclerosis flares,
indicating that the vaccine promotes autoimmune reactions against healthy
tissue.
SARS-CoV-2 Spike does not only bind to ACE2. It was
suspected to have regions that bind to basigin, integrins, neuropilin-1, and bacterial lipopolysaccharides
as well. SARS-CoV-2 Spike, on its own, can potentially bind any of these things
and act as a ligand for them, triggering unspecified
and likely highly inflammatory cellular activity.
SARS-CoV-2 Spike contains an unusual PRRA insert that forms a furin cleavage site. Furin is a
ubiquitous human protease, making this an ideal property for the Spike to have,
giving it a high degree of cell tropism. No wild-type SARS-like coronaviruses related to SARS-CoV-2 possess this feature,
making it highly suspicious, and perhaps a sign of human tampering.
SARS-CoV-2 Spike has a prion-like domain that
enhances its infectiousness.
The Spike S1 RBD may bind to heparin-binding proteins and promote amyloid aggregation. In humans, this could lead to
Parkinson’s, Lewy Body Dementia, premature
Alzheimer’s, or various other neurodegenerative diseases. This is very
concerning because SARS-CoV-2 S1 is capable of injuring and penetrating the
blood-brain barrier and entering the brain. It is also capable of increasing
the permeability of the blood-brain barrier to other molecules.
SARS-CoV-2, like other betacoronaviruses, may have
Dengue-like ADE, or antibody-dependent enhancement of disease. For those who
aren’t aware, some viruses, including betacoronaviruses,
have a feature called ADE. There is also something called Original Antigenic
Sin, which is the observation that the body prefers to produce antibodies based
on previously-encountered strains of a virus over newly-encountered ones.
In ADE, antibodies from a previous infection become
non-neutralizing due to mutations in the virus’s proteins. These
non-neutralizing antibodies then act as trojan
horses, allowing live, active virus to be pulled into macrophages through their
Fc receptor pathways, allowing the virus to infect
immune cells that it would not have been able to infect before. This has been
known to happen with Dengue Fever; when someone gets sick with Dengue,
recovers, and then contracts a different strain, they can get very, very ill.
If someone is vaccinated with mRNA based on the Spike
from the initial Wuhan strain of SARS-CoV-2, and then they become infected with
a future, mutated strain of the virus, they may become severely ill. In other
words, it is possible for vaccines to sensitize someone to disease.
There is a precedent for this in recent history. Sanofi’s
Dengvaxia vaccine for Dengue failed because it caused
immune sensitization in people whose immune systems were Dengue-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 12 th , 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 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 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 9 th , 2020, Charles Lieber, a Harvard
nanotechnology researcher with decades of experience, was indicted by the DOJ
for fraud. Charles Lieber received millions of
dollars in grant money from the US Department of Defense, specifically the
military think tanks DARPA, AFOSR, and ONR, as well as NIH and MITRE. His
specialty is the use of silicon nanowires in lieu of
patch clamp electrodes to monitor and
modulate intracellular activity, something he has been working on at Harvard for
the past twenty years. He was claimed to have been working on silicon nanowire batteries in China, but none of his colleagues can
recall him ever having worked on battery technology in his life; all of his
research deals with bionanotechnology, or the blending
of nanotech with living cells.
The indictment was over his collaboration with the Wuhan University of
Technology. He had double-dipped, against the terms of his DOD grants, and
taken money from the PRC’s Thousand Talents plan, a program which the Chinese
government uses to bribe Western scientists into sharing proprietary R&D information
that can be exploited by the PLA for strategic advantage.
Charles Lieber’s own papers describe the use of
silicon nanowires for brain-computer interfaces, or “neural
lace” technology. His papers describe how neurons can endocytose
whole silicon nanowires or parts of them, monitoring
and even modulating neuronal activity.
Charles Lieber was a colleague of Robert Langer.
Together, along with Daniel S. Kohane, they worked on
a paper describing artificial tissue scaffolds that could be implanted in a
human heart to monitor its activity remotely.
Robert Langer, an MIT alumnus and expert in nanotech drug
delivery, is one of the co-founders of Moderna. His
net worth is now $5.1 billion USD thanks to Moderna’s
mRNA-1273 vaccine sales.
Both Charles Lieber and Robert
Langer’s bibliographies describe, essentially, techniques for human enhancement,
i.e. transhumanism. Klaus Schwab, the founder of the
World Economic Forum and the architect behind the so-called “Great Reset”, has
long spoken of the “blending of biology and machinery” in his books.
Since these revelations, it has come to the attention of
independent researchers that the COVID-19 vaccines may contain reduced graphene oxide nanoparticles.
Japanese researchers have also found unexplained contaminants in COVID-19
vaccines.
Graphene
oxide is an anxiolytic. It has been shown to reduce
the anxiety of laboratory mice when injected into their brains. Indeed, given
SARS-CoV-2 Spike’s propensity to compromise the blood-brain barrier and
increase its permeability, it is the perfect protein for preparing brain tissue
for extravasation of nanoparticles
from the bloodstream and into the brain. Graphene is
also highly conductive and, in some circumstances, paramagnetic.
In 2013, under the Obama administration, DARPA launched
the BRAIN Initiative; BRAIN is an acronym for Brain Research Through Advancing
Innovative Neurotechnologies®. This program involves
the development of brain-computer interface technologies for the military,
particularly non-invasive, injectable systems that
cause minimal damage to brain tissue when removed. Supposedly, this technology
would be used for healing wounded soldiers with traumatic brain injuries, the
direct brain control of prosthetic limbs, and even new abilities such as
controlling drones with one’s mind.
Various methods have been proposed for achieving this, including optogenetics, magnetogenetics, ultrasound,
implanted electrodes, and transcranial
electromagnetic stimulation. In all instances, the goal is to obtain read or
read-write capability over neurons, either by stimulating and probing them, or
by rendering them especially sensitive to stimulation and probing.
However, the notion of the widespread use of BCI technology, such as Elon Musk’s Neuralink device, raises
many concerns over privacy and personal autonomy. Reading from neurons is
problematic enough on its own. Wireless brain-computer interfaces may interact
with current or future wireless GSM infrastructure, creating neurological data
security concerns. A hacker or other malicious actor may compromise such
networks to obtain people’s brain data, and then exploit it for nefarious
purposes.
However, a device capable of writing to human neurons, not just reading from
them, presents another, even more serious set of ethical concerns. A BCI that
is capable of altering the contents of one’s mind for innocuous purposes, such
as projecting a heads-up display onto their brain’s visual center or sending audio
into one’s auditory cortex, would also theoretically be capable of altering
mood and personality, or perhaps even subjugating someone’s very will,
rendering them utterly obedient to authority. This technology would be a
tyrant’s wet dream. Imagine soldiers who would shoot their own countrymen without
hesitation, or helpless serfs who are satisfied to live in literal dog kennels.
BCIs could be used to unscrupulously alter perceptions of basic things such as
emotions and values, changing people’s thresholds of satiety, happiness, anger,
disgust, and so forth. This is not inconsequential. Someone’s entire regime of
behaviors could be altered by a BCI, including such things as suppressing their
appetite or desire for virtually anything on Maslow’s Hierarchy of Needs.
Anything is possible when you have direct access to someone’s brain and its
contents. Someone who is obese could be made to feel disgust at the sight of
food. Someone who is involuntarily celibate could have their libido disabled so
they don’t even desire sex to begin with. Someone who is racist could be forced
to feel delight over cohabiting with people of other races. Someone who is
violent could be forced to be meek and submissive. These things might sound
good to you if you are a tyrant, but to normal people, the idea of personal
autonomy being overridden to such a degree is appalling.
For the wealthy, neural laces would be an unequaled boon,
giving them the opportunity to enhance their intelligence with neuroprosthetics (i.e. an “exocortex”),
and to deliver irresistible commands directly into the minds of their
BCI-augmented servants, even physically or sexually abusive commands that they
would normally refuse.
If the vaccine is a method to surreptitiously introduce
an injectable BCI into millions of people without their
knowledge or consent, then what we are witnessing is the rise of a tyrannical
regime unlike anything ever seen before on the face of this planet, one that
fully intends to strip every man, woman, and child of our free will.
Our flaws are what make us human. A utopia arrived at by removing people’s free
will is not a utopia at all. It is a monomaniacal nightmare. Furthermore, the
people who rule over us are Dark Triad types who cannot be trusted with such power.
Imagine being beaten and sexually assaulted by a wealthy and powerful
psychopath and being forced to smile and laugh over it because your neural lace
gives you no
choice but to obey your master.
The Elites are forging ahead with this technology without giving people any
room to question the social or ethical ramifications, or to establish
regulatory frameworks that ensure that our personal agency and autonomy will
not be overridden by these devices. They do this because they secretly dream of
a future where they can treat you worse than an animal and you cannot even
fight back. If this evil plan is allowed to continue, it will spell the end of
humanity as we know it.
Conclusions:
The current pandemic was produced and perpetuated by the establishment, through
the use of a virus engineered in a PLA-connected Chinese biowarfare
laboratory, with the aid of American taxpayer dollars and French expertise.
This research was conducted under the absolutely
ridiculous euphemism of “gain-of-function” research, which is supposedly
carried out in order to determine which viruses have the highest potential for zoonotic spillover and preemptively vaccinate or guard
against them.
Gain-of-function/gain-of-threat research, a.k.a.
“Dual-Use Research of Concern”, or DURC, is bioweapon
research by another, friendlier-sounding name, simply
to avoid the taboo of calling it what it actually is.It
has always been bioweapon research. The people who
are conducting this research fully understand that they are taking wild
pathogens that are not infectious in humans and making them more infectious, often
taking grants from military think tanks encouraging them to do so.
These virologists conducting this type of research are enemies of their fellow
man, like pyromaniac firefighters. GOF research has never protected anyone from
any pandemic. In fact, it has now started one, meaning its utility for
preventing pandemics is actually negative. It should have been banned globally,
and the lunatics performing it should have been put in straitjackets long ago.
Either through a leak or an intentional release from the
Wuhan Institute of Virology, a deadly SARS strain is now endemic across the
globe, after the WHO and CDC and public officials first downplayed the risks,
and then intentionally incited a panic and lockdowns that jeopardized people’s
health and their livelihoods.
This was then used by the utterly depraved and
psychopathic aristocratic class who rule over us as an excuse to coerce people
into accepting an injected poison which may be a depopulation agent, a mind control/pacification
agent in the form of injectable “smart dust”, or both
in one. They believe they can get away with this by weaponizing
the social stigma of vaccine refusal. They are incorrect.
Their motives are clear and obvious to anyone who has
been paying attention. These megalomaniacs have raided the pension funds of the
free world. Wall Street is insolvent and has had an ongoing liquidity crisis
since the end of 2019. The aim now is to exert total, full-spectrum physical,
mental, and financial control over humanity before we realize just how badly
we’ve been extorted by these maniacs.
The
pandemic and its response served multiple purposes for the Elite:
• Concealing a depression
brought on by the usurious plunder of our economies conducted by rentier-capitalists and absentee owners who produce
absolutely nothing of any value to society whatsoever. Instead of us having a
very predictable Occupy Wall Street Part II, the Elites and their stooges got to
stand up on television and paint themselves as wise and all-powerful saviors instead
of the marauding cabal of despicable land pirates that they are.
• Destroying small businesses and eroding the middle class.
• Transferring trillions of dollars of wealth from the American public and into
the pockets of billionaires and special interests.
• Engaging in insider trading, buying stock in biotech companies and shorting
brick-and-mortar businesses and travel companies, with the aim of collapsing
face-to-face commerce and tourism and replacing it with e-commerce and servitization.
• Creating a casus belli for war with China, encouraging us to attack them,
wasting American lives and treasure and driving us to the brink of nuclear armageddon.
• Establishing technological and biosecurity
frameworks for population control and technocratic-socialist “smart cities”
where everyone’s movements are despotically tracked, all in anticipation of
widespread automation, joblessness, and food shortages, by using the false guise
of a vaccine to compel cooperation.
Any one of these things would constitute a vicious rape
of Western society. Taken together, they beggar belief; they are a complete
inversion of our most treasured values.
What is the purpose of all of this? One can only
speculate as to the perpetrators’ motives, however, we have some theories.
The Elites are trying to pull up the ladder, erase upward
mobility for large segments of the population, cull political opponents and
other “undesirables”, and put the remainder of humanity on a tight leash, rationing
our access to certain goods and services that they have deemed “high-impact”,
such as automobile use, tourism, meat consumption, and so on. Naturally, they
will continue to have their own
luxuries, as part of a strict caste system akin to feudalism.
Why are they doing this? Simple.
The Elites are Neo-Malthusians and believe that we are overpopulated and that
resource depletion will collapse civilization in a matter of a few short
decades. They are not necessarily incorrect in this belief. We are
overpopulated, and we are consuming too many resources.
However, orchestrating such a gruesome and murderous power grab in response to
a looming crisis demonstrates that they have nothing but the utmost contempt
for their fellow man.
To those who are participating in this disgusting farce
without any understanding of what they are doing, we have one word for you.
Stop. You are causing irreparable harm to your country and to your fellow
citizens.
To those who may be reading this warning and have full
knowledge and understanding of what they are doing and how it will unjustly
harm millions of innocent people, we have a few more words.
Damn you to hell. You will not destroy America and the
Free World, and you will not have your New World Order. We will make certain of
that.
References:
COVID-19
is not a viral pneumonia — it is a viral vascular endotheliitis:
https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)30937-5/fulltext
https://academic.oup.com/eurheartj/article/41/32/3038/5901158
https://www.embopress.org/doi/full/10.15252/embr.202152744
COVID-19
is not just a respiratory disease — it can precipitate multiple organ failure,
including hypoxic and inflammatory damage to various vital organs, such as the
brain, heart, liver, pancreas, kidneys, and intestines:
https://www.nature.com/articles/d41586-021-01693-6
https://www.health.harvard.edu/blog/the-hidden-long-term-cognitive-effects-of-covid-2020100821133
https://www.nature.com/articles/s41422-020-0390-x
https://www.embopress.org/doi/full/10.15252/embj.2020106230
https://jamanetwork.com/journals/jama/fullarticle/2776538
https://pubmed.ncbi.nlm.nih.gov/32921216/
https://www.nature.com/articles/s41575-021-00426-4
https://pubmed.ncbi.nlm.nih.gov/32553666/
https://www.nature.com/articles/s41467-021-23886-3
https://pubmed.ncbi.nlm.nih.gov/34081912/
https://www.nature.com/articles/s41581-021-00452-0
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438210/
https://www.nature.com/articles/s41598-021-92740-9
Some
of the most common laboratory findings in COVID-19:
https://www.uptodate.com/contents/covid-19-clinical-features
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426219/
COVID-19
can present as almost anything:
https://www.nature.com/articles/s41591-020-0968-3
https://www.frontiersin.org/articles/10.3389/fmed.2020.00526/full
COVID-19
is more severe in those with conditions that involve endothelial dysfunction,
such as obesity, hypertension, and diabetes:
https://jamanetwork.com/journals/jama/fullarticle/2772071
https://mdpi-res.com/d_attachment/cells/cells-10-00933/article_deploy/cells-10-00933.pdf
The
vast majority of COVID-19 cases are mild and do not
cause significant disease:
https://www.webmd.com/lung/covid-recovery-overview#1
https://academic.oup.com/ofid/article/7/9/ofaa286/5875595
https://pubmed.ncbi.nlm.nih.gov/33289900/
In
those who have critical COVID-19-induced sepsis, hypoxia, coagulopathy,
and ARDS, the most common treatments are intubation, injected corticosteroids,
and blood thinners like heparin, which often precipitate harmful hemorrhages:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7548860/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448713/
https://www.nejm.org/doi/full/10.1056/NEJMoa2103417
The
majority of people who go on a ventilator are dying due to COVID-19 mimicking
the physiology of ischemia-reperfusion injury with prolonged transient hypoxia
and ischemia, leading directly to the formation of damaging reactive oxygen
species:
https://www.journalofsurgicalresearch.com/article/S0022-4804(14)00176-0/fulltext
https://www.nature.com/articles/nature13909
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625011/
https://www.atsjournals.org/doi/full/10.1164/rccm.201401-0168CP
https://pubmed.ncbi.nlm.nih.gov/18974366/
The
end-stage of COVID-19 is severe lipid peroxidation,
where fats in the body start to “rust” due to damage by oxidative stress:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768996/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357498/
https://www.liebertpub.com/doi/10.1089/ars.2021.0017
Oxidized
lipids appear as foreign objects to the immune system, which recognizes and
forms antibodies against OSEs, or oxidation-specific epitopes:
https://ard.bmj.com/content/annrheumdis/early/2020/08/04/annrheumdis-2020-218145.full.pdf
https://ard.bmj.com/content/80/9/1236
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7256550/
https://www.hss.edu/conditions_top-ten-series-antiphospholipid-syndrome-coronavirus-covid-19.asp
In
COVID-19, neutrophil degranulation
and NETosis in the bloodstream drives severe
oxidative damage; hemoglobin becomes incapable of carrying oxygen due to heme iron being stripped out of heme
by hypochlorous acid:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757048/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7436665/
https://www.nature.com/articles/s41418-021-00805-z
https://www.sciencedirect.com/science/article/pii/S221249262030052X
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
and blood pressure in the body and in the bloodstream by controlling
sodium/potassium
retention
and excretion and vascular tone:
https://www.ncbi.nlm.nih.gov/books/NBK470410/
https://www.merckmanuals.com/home/multimedia/figure/cvs_regulating_blood_pressure_renin
This
protein, ACE2, is ubiquitous in every part of the body that interfaces with the
circulatory system, particularly in vascular endothelial cells and pericytes, brain astrocytes,
renal tubules and podocytes, pancreatic islet cells,
bile duct and intestinal epithelial cells, and the seminiferous
ducts of the testis, all of which SARS-CoV-2 can infect:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7167720/
https://www.frontiersin.org/articles/10.3389/fmed.2020.594495/full
https://www.frontiersin.org/articles/10.3389/fneur.2020.573095/full
SARS-CoV-2
infects a cell as follows:
https://www.nature.com/articles/s41401-020-0485-4
https://www.science.org/doi/10.1126/science.abb2507
https://www.sciencedirect.com/science/article/abs/pii/S1931312820306211
SARS-CoV-2
Spike proteins embedded in a cell can actually cause adjacent human cells to
fuse together, forming syncytia/MGCs:
https://www.nature.com/articles/s41418-021-00782-3
https://pubmed.ncbi.nlm.nih.gov/33051876/
SARS-CoV-2’s
viroporins, such as its Envelope protein, act as
calcium ion channels, introducing calcium into infected cells:
https://www.nature.com/articles/s41422-021-00519-4
https://virologyj.biomedcentral.com/articles/10.1186/s12985-019-1182-0
The
virus suppresses the natural interferon response, resulting in delayed
inflammation:
https://www.nature.com/articles/s12276-021-00592-0
https://mdpi-res.com/d_attachment/viruses/viruses-12-01433/article_deploy/viruses-12-01433.pdf
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310780/
SARS-CoV-2
N protein can also directly activate the NLRP3 inflammasome:
https://www.nature.com/articles/s41467-021-25015-6
https://www.frontiersin.org/articles/10.3389/fimmu.2020.01021/full
SARS-CoV-2
suppresses the Nrf2 antioxidant pathway, reducing the body’s own endogenous
antioxidant enzyme activity:
https://www.nature.com/articles/s41467-020-18764-3
https://ctajournal.biomedcentral.com/articles/10.1186/s13601-020-00362-7
https://mdpi-res.com/d_attachment/ijms/ijms-22-07963/article_deploy/ijms-22-07963.pdf
The
suppression of ACE2 by binding with Spike causes a buildup of bradykinin that would otherwise be broken down by ACE2:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7834250/
https://www.the-scientist.com/news-opinion/is-a-bradykinin-storm-brewing-in-covid-19--67876
This
constant calcium influx into the cells results in (or is accompanied by)
noticeable hypocalcemia, or low blood calcium:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292572/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041474/
https://www.sciencedirect.com/science/article/abs/pii/S1871402121000059
Bradykinin upregulates
cAMP, cGMP, COX, and Phospholipase C activity. This results in prostaglandin release
and vastly increased intracellular calcium signaling, which promotes highly
aggressive ROS release and ATP depletion:
https://www.sciencedirect.com/science/article/abs/pii/S089158490700319X?via%3Dihub
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1218972/
https://pubmed.ncbi.nlm.nih.gov/2156053/
https://www.sciencedirect.com/topics/medicine-and-dentistry/bradykinin-b2-receptor-agonist
https://www.sciencedirect.com/topics/neuroscience/bradykinin
NADPH
oxidase releases superoxide into the extracellular
space:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556774/
https://www.pnas.org/content/110/21/8744
Superoxide
radicals react with nitric oxide to form peroxynitrite:
https://pubmed.ncbi.nlm.nih.gov/8944624/
https://www.pnas.org/content/115/23/5839
Peroxynitrite reacts with the tetrahydrobiopterin
cofactor needed by endothelial nitric oxide synthase,
destroying it and “uncoupling” the eNOS enzymes,
causing nitric oxide synthase to synthesize more superoxide
instead (this means that every process that upregulates
NOS activity now produces superoxide instead of nitric oxide):
https://pubmed.ncbi.nlm.nih.gov/24353182/
https://academic.oup.com/cardiovascres/article/73/1/8/316487
https://pubs.acs.org/doi/10.1021/bi9016632
This
proceeds in a positive feedback loop until nitric oxide bioavailability in the
circulatory system is depleted:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276137/
Dissolved
nitric oxide gas produced constantly by eNOS serves
many important functions, but it is also antiviral against SARS-like coronaviruses, preventing the palmitoylation
of the viral Spike protein and making it harder for it to bind to host
receptors:
https://journal.chestnet.org/article/S0012-3692(20)34397-X/fulltext
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111989/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754882/
The
loss of NO allows the virus to begin replicating with impunity in the body
(clearly, the virus has an evolutionary incentive to induce oxidative stress to
destroy nitric oxide):
Those
with endothelial dysfunction (i.e. hypertension, diabetes, obesity, old age,
African-American race) have redox equilibrium issues
to begin with, giving the virus an advantage:
https://www.nature.com/articles/s41392-020-00454-7
https://www.frontiersin.org/articles/10.3389/fphys.2020.605908/full
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430889/
https://pubmed.ncbi.nlm.nih.gov/19004510/
Due
to the extreme cytokine release triggered by these processes, the body summons a great deal of neutrophils
and monocyte-derived alveolar macrophages to the
lungs:
https://www.frontiersin.org/articles/10.3389/fimmu.2021.652470/full
https://www.frontiersin.org/articles/10.3389/fimmu.2021.720109/full
Phagocytic cells of the innate immune system
are the first-line defenders against pathogens. They work by engulfing invaders
and trying to attack them with enzymes that produce powerful oxidants, like SOD
and MPO:
https://www.frontiersin.org/articles/10.3389/fimmu.2012.00174/full
https://jlb.onlinelibrary.wiley.com/doi/full/10.1189/jlb.0809549
Superoxide
dismutase takes superoxide and makes hydrogen peroxide, and myeloperoxidase
takes hydrogen peroxide and chlorine ions and makes hypochlorous
acid, which is many, many times more reactive than sodium hypochlorite bleach:
https://www.sciencedirect.com/topics/neuroscience/superoxide-dismutase
https://www.sciencedirect.com/topics/medicine-and-dentistry/myeloperoxidase
In
severe and critical COVID-19, there is actually rather severe NETosis:
https://www.frontiersin.org/articles/10.3389/fphar.2021.708302/full
https://insight.jci.org/articles/view/138999
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184981/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488868/
https://www.sciencedirect.com/science/article/pii/S221249262030052X
Hypochlorous acid building up in the bloodstream
begins to bleach the iron out of heme and compete for
O2 binding sites. Red blood cells lose the ability to transport oxygen, causing
the sufferer to turn blue in the face:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757048/
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0120737
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863623/
Unliganded iron, hydrogen peroxide, and
superoxide in the bloodstream undergo the Haber-Weiss and Fenton reactions,
producing extremely reactive hydroxyl radicals that violently strip electrons
from surrounding fats and DNA, oxidizing them severely:
https://www.sciencedirect.com/science/article/pii/S0753332221000135
https://sites.kowsarpub.com/ans/articles/60038.html
https://www.sciencedirect.com/science/article/abs/pii/S0300483X00002316?via%3Dihub
https://www.sciencedirect.com/topics/chemistry/fenton-reaction
This
condition is not unknown to medical science. The actual name for all of this is
acute sepsis (but without the traditional hallmarks of sepsis, like shock):
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056356/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886971/
https://www.futuremedicine.com/doi/10.2217/fmb-2020-0312
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 alondialdehyde:
https://onlinelibrary.wiley.com/doi/full/10.1002/ehf2.12958
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264936/
https://www.sciencedirect.com/science/article/pii/S2213231721001300
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180845/
When
you intubate someone with this condition, you are
setting off a free radical bomb by supplying the cells with O2. It’s a
catch-22, because we need oxygen to make Adenosine Triphosphate
(that is, to live), but O2 is also the precursor of all these damaging radicals
that lead to lipid peroxidation:
https://www.nature.com/articles/pr2009174
The
correct treatment for severe COVID-19 related sepsis is non-invasive
ventilation, steroids, and antioxidant infusions:
https://covid19criticalcare.com/covid-19-protocols/math-plus-protocol/
https://mdpi-res.com/d_attachment/medicina/medicina-56-00619/article_deploy/medicina-56-00619-v2.pdf
Most
of the drugs repurposed for COVID-19 that show any benefit whatsoever in
rescuing critically-ill COVID-19 patients are antioxidants. N-acetylcysteine, melatonin, fluvoxamine,
budesonide, famotidine, cimetidine, and ranitidine are all antioxidants:
https://www.hindawi.com/journals/omcl/2018/6581970/
https://www.intechopen.com/chapters/62672
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708076/
https://www.karger.com/Article/Abstract/88623
https://www.sciencedirect.com/science/article/abs/pii/000629529390218L?via%3Dihub
Indomethacin prevents iron-driven oxidation of arachidonic acid to isoprostanes:
https://www.sciencedirect.com/science/article/abs/pii/0161463079900442
There
are powerful antioxidants such as apocynin that have
not even been tested on COVID-19 patients yet which could defang neutrophils, prevent lipid peroxidation,
restore endothelial health, and restore oxygenation to the tissues:
https://link.springer.com/article/10.1007/s10787-020-00715-5
Scientists
who know anything about pulmonary neutrophilia, ARDS,
and redox biology have known or surmised much of this
since March 2020:
https://www.researchgate.net/post/NADPH_oxidase_Covid-19_Oxygen_treatment
In
April 2020, Swiss scientists confirmed that COVID-19 was a systemic vascular endotheliitis:
https://www.usz.ch/en/covid-19-also-a-systemic-endotheliitis/
By
late 2020, experts had already concluded that COVID-19 causes a form of viral
sepsis:
https://www.healthleadersmedia.com/clinical-care/expert-severe-covid-19-illness-viral-sepsis
https://wentworthreport.com/2021/09/11/ivermectin-wins-in-india/
https://ivmmeta.com
The
Indian Bar Association of Mumbai has brought criminal
charges against WHO Chief Scientist Dr. Soumya Swaminathan for recommending against the use of Ivermectin:
https://indianbarassociation.in/wp-content/uploads/2021/05/IBA-PRESS-RELEASE-MAY-26-2021.pdf
Ivermectin is not “horse dewormer”.
Yes, it is sold in veterinary paste form as a dewormer
for animals. It has also been available in pill form for humans for decades, as
an antiparasitic drug:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043740/
The
media have disingenuously claimed that because Ivermectin
is an antiparasitic drug, it has no utility as an
antivirus. This is incorrect. Ivermectin has utility
as an antiviral. It blocks importin, 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:
https://www.sciencedirect.com/science/article/abs/pii/S0166354219307211?via%3Dihub
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539925/
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:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7386240/
Billions
of dollars of utterly useless Remdesivir were sold to
our governments on the taxpayer’s dime, and it ended up being totally useless
for treating hyperinflammatory COVID-19:
https://www.forbes.com/sites/jvchamary/2021/01/31/remdesivir-covid-
coronavirus/?sh=7e6034e666c2
COVID-19
is airborne. The WHO carried water for China by claiming that the virus was
only droplet-borne. Our own CDC absurdly claimed that it was mostly transmitted
by fomite-to-face contact, which, given its rapid
spread from Wuhan to the rest of the world, would have been physically
impossible:
https://www.thelancet.com/article/S0140-6736(21)00869-2/fulltext
The
ridiculous belief in fomite-to-face being a primary
mode of transmission led to the use of surface disinfection protocols that
wasted time, energy, productivity, and disinfectant:
https://www.nature.com/articles/d41586-021-00251-4
The
6-foot guidelines are absolutely useless. The minimum safe distance to protect
oneself from an aerosolized virus is to be 15+ feet away from an infected
person, no closer. Realistically, no public transit is safe:
https://www.medrxiv.org/content/10.1101/2020.08.03.20167395v1
https://khn.org/news/fact-check-airborne-transmission-coronavirus-science-behind-aerosol-spread/
Surgical
masks do not protect you from aerosols. The virus is too small and the filter
media has too large of gaps to filter it out. They may catch respiratory
droplets and keep the virus from being expelled by someone who is sick, but
they do not filter a cloud of infectious aerosols if someone were to walk into said
cloud:
https://ajicjournal.org/retrieve/pii/S0196655305801439
The
minimum level of protection against this virus is quite literally a P100
respirator, a PAPR/CAPR, or a 40mm NATO CBRN respirator, ideally paired with a
full-body tyvek or tychem
suit, gloves, and booties, with all the holes and gaps taped (in a pinch,
surgical masks can be modified or worn a specific way to
increase
filtration):
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409952/
https://www.mopec.com/coronavirus-protection-made-easy-with-the-maxair-capr/
Live
SARS-CoV-2 may potentially be detected in sewage outflows, and there may be
oral-fecal
transmission:
https://www.sciencedirect.com/science/article/pii/S0048969720325936
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0249568
https://www.nature.com/articles/s41587-020-0684-z
During
the SARS outbreak in 2003, in the Amoy Gardens incident, hundreds of people
were infected by aerosolized fecal matter rising from floor drains in their
apartments (there is some valid concern that COVID-19 may also spread the same
way, given its similarities to SARS):
https://pubmed.ncbi.nlm.nih.gov/16696450/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC539564/
https://www.neha.org/sites/default/files/jeh/JEH5.06-Feature-Environmental-Transmission-of-SARS.pdf
https://www.cleanlink.com/news/article/COVID-19-Could-Spread-Through-Dry-Floor-Drains--25600
The
vaccines for COVID-19 are not sterilizing and do not prevent infection or
transmission. They are “leaky” vaccines. This means they remove the evolutionary
pressure on the virus to become less lethal. It also means that the vaccinated
are perfect carriers. In other words, those who are vaccinated are a
threat
to the unvaccinated, not the other way around:
https://www.cdc.gov/media/releases/2021/s0730-mmwr-covid-19.html
All
of the COVID-19 vaccines currently in use have undergone minimal testing, with
highly accelerated clinical trials. Though they appear to limit severe illness,
the long-term safety profile of these vaccines remains unknown:
https://www.jdsupra.com/legalnews/accelerated-covid-19-vaccine-clinical-95853/
https://www.nebraskamed.com/COVID/were-the-covid-19-vaccines-rushed
Some
of these so-called “vaccines” utilize an untested new technology that has never
been used in vaccines before. Traditional vaccines use weakened or killed virus
to stimulate an immune response. The Moderna and
Pfizer-BioNTech vaccines do not. They are purported
to consist of an intramuscular shot containing a suspension of lipid nanoparticles filled with messenger RNA:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439223/
https://cen.acs.org/pharmaceuticals/drug-delivery/Without-lipid-shells-mRNA-vaccines/99/i8
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/different-vaccines/mrna.html
https://medlineplus.gov/genetics/understanding/therapy/mrnavaccines/
The
way they generate an immune response is by fusing with cells in a vaccine
recipient’s shoulder, undergoing endocytosis,
releasing their mRNA cargo into those cells, and then utilizing the ribosomes in those cells to synthesize modified SARS-CoV-2
Spike proteins in-situ:
https://www.nature.com/articles/s41586-020-2622-0
These
vaccines were produced or validated with the aid of fetal cell lines HEK-293
and PER.C6, which people with certain religious convictions may object strongly
to:
https://cmda.org/the-ethics-of-the-sars-cov-2-vaccines-revisited/SARS-CoV-2
Spike
is a highly pathogenic protein on its own. It is impossible to overstate the
danger presented by introducing this protein into the human body:
It
is claimed by vaccine manufacturers that the vaccine remains in cells in the
shoulder, and that SARS-CoV-2 Spike produced and expressed by these cells from
the vaccine’s genetic material is harmless and inert, thanks to the insertion
of prolines in the Spike sequence to stabilize it in
the prefusion conformation, preventing the Spike from
becoming active and fusing with other cells:
https://www.nature.com/articles/s41467-020-20321-x
https://cen.acs.org/pharmaceuticals/vaccines/tiny-tweak-behind-COVID-19/98/i38
However,
a pharmacokinetic study from Japan showed that the lipid nanoparticles and
mRNA from the Pfizer vaccine did not stay in the shoulder, and in fact bioaccumulated in many different organs, including the
reproductive organs and adrenal glands, meaning that modified Spike is being
expressed
quite
literally all over the place:
https://files.catbox.moe/0vwcmj.pdf
These lipid nanoparticles
may trigger anaphylaxis in an unlucky few:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441754/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862013/
Messenger
RNA is normally consumed right after it is produced in the body, being
translated into a protein by a ribosome. COVID-19 vaccine mRNA
is produced outside the body, long before a ribosome translates it. In the
meantime, it could accumulate damage if inadequately preserved. When a ribosome
attempts to translate a damaged strand of mRNA, it can become stalled:
https://elifesciences.org/articles/61984
https://www.frontiersin.org/articles/10.3389/fgene.2018.00431/full
Certain
proteins, including SARS-CoV-2 Spike, have proteolytic
cleavage sites that are basically like little dotted lines that say “cut here”,
which attract a living organism’s own proteases (essentially, molecular scissors)
to cut them. There is a possibility that S1 may be proteolytically
cleaved from S2, causing active
S1
to float away into the bloodstream while leaving the S2 “stalk” embedded in the
membrane of the cell that expressed the protein:
https://academic.oup.com/cid/advance-article/doi/10.1093/cid/ciab465/6279075
https://www.nature.com/articles/s41564-021-00908-w
https://www.life-science-alliance.org/content/3/9/e202000786
SARS-CoV-2
Spike has a Superantigenic region (SAg), which may promote extreme inflammation:
https://www.pnas.org/content/117/41/25254
https://www.nature.com/articles/s41577-021-00502-5
Anti-Spike
antibodies were found in one study to function as autoantibodies
and attack the body’s own cells:
https://www.researchsquare.com/article/rs-612103/v2
Those
who have been immunized with COVID-19 vaccines have developed blood clots, myocarditis, Guillain-Barre
Syndrome, Bell’s Palsy, and multiple sclerosis flares, indicating that the
vaccine promotes autoimmune reactions against healthy tissue:
https://drrichswier.com/2021/09/18/summary-covid-19-vaccine-concerns/
https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-july-13-2021
https://www.medpagetoday.com/infectiousdisease/covid19vaccine/94061?xid=nl_mpt_DHE_2021-08-17
SARS-CoV-2
Spike does not only bind to ACE2. It was suspected to have regions that bind to
basigin, integrins,
neuropilin-1, and bacterial lipopolysaccharides as
well:
https://www.nature.com/articles/s41564-021-00958-0
https://www.mdpi.com/1422-0067/22/3/992/pdf
https://pubs.acs.org/doi/10.1021/acschemneuro.0c00619
https://www.science.org/doi/full/10.1126/science.abd3072
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0253347
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7799037/
SARS-CoV-2
Spike, on its own, can potentially bind any of these things and act as a ligand for them, triggering unspecified and likely highly
inflammatory cellular activity:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827936/
SARS-CoV-2
Spike contains an unusual PRRA insert that forms a furin
cleavage site. Furin is a ubiquitous human protease,
making this an ideal property for the Spike to have, giving it a high degree of
cell tropism. No wild-type SARS-like coronaviruses
related to SARS-CoV-2 possess this feature, making it highly suspicious, and
perhaps a sign of human tampering:
https://journals.asm.org/doi/full/10.1128/JVI.01751-20
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457603/
SARS-CoV-2
Spike has a prion-like domain that enhances its
infectiousness:
https://www.preprints.org/manuscript/202003.0422/v1
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0023664
The
Spike S1 RBD may bind to heparin-binding proteins and promote amyloid aggregation. In humans, this could lead to
Parkinson’s, Lewy Body Dementia, premature
Alzheimer’s, or various other neurodegenerative diseases:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988450/
This
is very concerning because SARS-CoV-2 S1 is capable of penetrating the
blood-brain barrier and entering the brain. It is capable of increasing the
permeability of the blood-brain barrier to itself and other molecules by
injuring and disrupting it directly:
https://www.nature.com/articles/s41593-020-00771-8
https://www.nature.com/articles/s41392-021-00719-9
https://pubmed.ncbi.nlm.nih.gov/33053430/
SARS-CoV-2,
like other betacoronaviruses, may have Dengue-like
ADE, or antibody-dependent enhancement of disease:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943455/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7454712/
https://www.journalofinfection.com/article/S0163-4453(21)00392-3/fulltext
https://sharylattkisson.com/2021/08/study-why-so-many-vaccinated-people-are-getting-sick/
https://www.nature.com/articles/s41564-020-00789-5
https://www.sciencedirect.com/science/article/pii/S1201971220307311
https://pubmed.ncbi.nlm.nih.gov/31826992/
https://www.biorxiv.org/content/10.1101/2021.08.22.457114v1
There is something
called Original Antigenic Sin, which is the observation that the body prefers
to produce antibodies based on previously-encountered strains of a virus over
newly-encountered ones:
https://www.jimmunol.org/content/202/2/335
https://en.wikipedia.org/wiki/Original_antigenic_sin
In ADE, antibodies
from a previous infection become non-neutralizing due to mutations in the
virus’s proteins. These non-neutralizing antibodies then act as trojan horses, allowing live,
active virus to be pulled into macrophages through their Fc
receptor pathways:
https://en.wikipedia.org/wiki/Antibody-dependent_enhancement
https://www.cdc.gov/dengue/training/cme/ccm/page57857.html
It is possible for
vaccines to sensitize someone to disease. There is a precedent for this in
recent history. Sanofi’s Dengvaxia
vaccine for Dengue failed because it caused immune sensitization in people
whose immune systems were Dengue-naïve:
https://www.frontiersin.org/articles/10.3389/fcimb.2020.572681/full
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739535/
In mice immunized
against SARS-CoV and challenged with the virus, a
close relative of SARS-CoV-2, they developed immune sensitization, Th2 immunopathology, and eosinophil
infiltration in their lungs:
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0035421
We have been told
that SARS-CoV-2 mRNA vaccines cannot be integrated into the human genome, because
messenger RNA cannot be turned back into DNA. This is false. There are elements
in human cells called LINE-1 retrotransposons, which
can indeed integrate mRNA into a human genome by endogenous
reverse transcription:
https://pubmed.ncbi.nlm.nih.gov/33330870/
https://home.solari.com/deep-state-tactics-101-the-covid-injection-fraud-its-not-a-vaccine/
The vaccine and the
virus were made by the same people. In 2014, there was a moratorium on SARS gain-of-function
research that lasted until 2017:
https://www.phe.gov/s3/dualuse/documents/gain-of-function.pdf
Ralph Baric is a
virologist and SARS expert at UNC Chapel Hill in North Carolina. This is who
Anthony Fauci was referring to when he insisted,
before Congress, that if any gain-of-function research was being conducted, it
was being conducted in North Carolina:
https://sph.unc.edu/adv_profile/ralph-s-baric-phd/
https://alumni.unc.edu/news/ralph-baric-on-the-front-lines-of-coronavirus-for-three-decades/
Ralph Baric and Shi Zhengli are colleagues and have co-written papers together:
https://www.nature.com/articles/nm.3985/
Ralph Baric mentored
Shi Zhengli in his gain-of-function manipulation
techniques, particularly serial passage, which results in a virus that appears
as if it originated naturally. In other words, deniable bioweapons. Serial passage in humanized hACE2 mice
may have produced something like SARS-CoV-2:
https://usrtk.org/biohazards-blog/ralph-baric-emails/
https://www.paul.senate.gov/newsweek-op-ed-congress-must-pursue-answers-about-origin-covid-19
https://nymag.com/intelligencer/article/coronavirus-lab-escape-theory.html
The funding for the
gain-of-function research being conducted at the Wuhan Institute of Virology
came from Peter Daszak. Peter Daszak
runs an NGO called EcoHealth Alliance:
https://peterdaszak.com/interceptdocs.pdf
https://theintercept.com/2021/09/09/covid-origins-gain-of-function-research/
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:
https://nypost.com/2021/07/01/pentagon-gave-millions-to-ecohealth-alliance-for-wuhan-lab/
https://www.judicialwatch.org/press-releases/wuhan-lab-fauci-grants/
https://www.judicialwatch.org/documents/jw-v-nih-wuhan-june-2021-00696/
Chinese
scientists in Wuhan reported being routinely bitten and urinated on by
laboratory animals:
In
November of 2019, three technicians at the Wuhan Institute of Virology
developed symptoms consistent with a flu-like illness:
https://www.webmd.com/lung/news/20210524/wuhan-lab-researchers-illness
December
12 th, 2019, Ralph
Baric signed a Material Transfer Agreement (essentially, an NDA) to receive Coronavirus mRNA vaccine-related materials co-owned by Moderna and NIH:
https://s3.documentcloud.org/documents/6935295/NIH-Moderna-Confidential-Agreements.pdf
It
wasn’t until a whole month later, on January 11th, 2020, that China allegedly sent us
the sequence to what would become known as SARS-CoV-2:
https://www.sciencedaily.com/releases/2020/01/200131114748.htm
Moderna claims, rather absurdly, that they developed a working
vaccine from this sequence in under 48 hours:
https://www.businessinsider.com/moderna-designed-coronavirus-vaccine-in-2-days-2020-11
https://globalnews.ca/news/7492076/moderna-coronavirus-vaccine-technology-how-it-works/
https://nymag.com/intelligencer/2020/12/moderna-covid-19-vaccine-design.html
Stéphane Bancel,
the current CEO of Moderna, was formerly the CEO of bioMérieux, a French multinational corporation specializing
in medical diagnostic tech, founded by one Alain Mérieux:
https://en.wikipedia.org/wiki/St%C3%A9phane_Bancel
https://www.himss.org/global-conference/speaker-stephane-bancel
Alain
Mérieux was one of the individuals who was
instrumental in the construction of the Wuhan Institute of Virology’s P4 lab:
https://medicalxpress.com/news/2020-04-wuhan-lab-core-virus-controversy.html
http://english.whiov.cas.cn/ne/201712/t20171212_187624.html
The
sequence given as the closest relative to SARS-CoV-2, RaTG13, is not a real
virus. It is a forgery:
https://nerdhaspower.weebly.com/ratg13-is-fake.html
https://www.peakprosperity.com/forum-topic/scientific-history-of-ratg13/
The
animal reservoir of SARS-CoV-2 has never been found:
https://www.technologyreview.com/2021/03/26/1021263/bat-covid-coronavirus-cause-origin-wuhan/
The
FBI raided Allure Medical in Shelby Township north of Detroit for billing
insurance for “fraudulent COVID-19 cures”. The treatment they were using? Intravenous Vitamin C.
An antioxidant. Which, as described above, is an
entirely valid treatment for COVID-19-induced sepsis, and indeed, is now part
of
the
MATH+ protocol advanced by Dr. Paul E. Marik:
https://covid19criticalcare.com/covid-19-protocols/math-plus-protocol/
https://pubmed.ncbi.nlm.nih.gov/31978969/
https://www.sciencedirect.com/science/article/abs/pii/S0883944119316107?via%3Dihub
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:
https://onlinelibrary.wiley.com/doi/10.1111/j.1472-8206.2009.00810.x
https://www.sciencedirect.com/science/article/pii/S1347861319342203
The
FDA also attempted to take N-acetylcysteine, a
harmless amino acid supplement and antioxidant, off the shelves, compelling
Amazon to remove it from their online storefront:
https://www.naturalproductsinsider.com/regulatory/us-senator-npa-press-fda-nac-supplements
https://www.nutraingredients-usa.com/Article/2021/05/11/CRN-This-is-not-the-final-word-on-NAC
https://www.naturalproductsinsider.com/regulatory/amazon-confirms-plans-removing-nac-supplements
On
June 9 th, 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:
http://cml.harvard.edu/resources/research-sponsors
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:
https://www.harvardmagazine.com/2011/01/virus-sized-transistors
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:
https://news.harvard.edu/gazette/story/2012/01/reading-lifes-building-blocks/
https://news.harvard.edu/gazette/story/2019/07/harvard-researchers-present-nanowire-devices-update/
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 (this risk has been known for a
very long time):
https://www.justice.gov/usao-ma/pr/harvard-university-professor-indicted-false-statement-charges
https://www.nature.com/articles/d41586-020-00291-2
https://www.research.psu.edu/sites/default/files/FBI_Risks_To_Academia.pdf
https://www.drdavidzweig.com/wp-content/uploads/2020/05/Zweig-Kang-TTP.pdf
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:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531316/
https://spectrum.ieee.org/human-cells-eat-nanowires
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:
https://www.bostonherald.com/2012/08/29/theyve-got-the-beat-2/
Robert
Langer, an MIT alumnus and expert in nanotech drug delivery, is one of the
co-founders of Moderna:
https://www.modernatx.com/modernas-board-directors
His
net worth is now $5.1 billion USD thanks to Moderna’s
mRNA-1273 vaccine sales:
https://www.ceotodaymagazine.com/2020/11/modernas-stock-rally-makes-bob-langer-a-billionaire/
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 (and even some surgical masks) may contain reduced graphene oxide nanoparticles:
https://www.thelibertybeacon.com/graphene-oxide-the-vector-for-covid-19-democide/
https://www.orwell.city/2021/06/vaccination-vial-analysis-explained.html
https://www.nature.com/articles/s41428-020-0350-9
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141029/
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:
https://www.sciencedirect.com/science/article/pii/S0142961221001058
https://graphene-flagship.eu/graphene/news/soothing-the-symptoms-of-anxiety-with-graphene-oxide/
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:
https://pubs.acs.org/doi/10.1021/acsanm.8b02056
https://www.sciencedirect.com/science/article/pii/S0168365916303236
Graphene is also highly conductive and, in
some circumstances, paramagnetic:
https://www.livescience.com/graphene-hides-rare-magnetism.html
https://www.sciencedirect.com/science/article/pii/S0008622319305809
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474003/
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:
https://www.darpa.mil/program/our-research/darpa-and-the-brain-initiative
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:
https://www.darpa.mil/news-events/2019-05-20
Wireless
brain-computer interfaces may interact with current or future wireless GSM
infrastructure, creating neurological data security concerns:
https://waitbutwhy.com/2017/04/neuralink.html
https://www.frontiersin.org/articles/10.3389/fnins.2019.00112/full
https://www.intechopen.com/chapters/44252
https://www.brown.edu/news/2021-03-31/braingate-wireless
A BCI that is capable
of altering the contents of one’s mind would theoretically be capable of
altering mood and personality, or perhaps even subjugating someone’s very will,
rendering them utterly obedient to authority:
https://link.springer.com/article/10.1007/s11023-012-9298-7
https://privacysos.org/technologies_of_controlmind_reading/
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:
http://www.buffalo.edu/news/releases/2010/07/11518.html
https://sitn.hms.harvard.edu/flash/2019/brain-machine-interfaces-may-used-study-regulate-mood/
https://www.nature.com/articles/s41593-019-0488-y
For the wealthy,
neural laces would be an unequaled boon, giving them the opportunity to enhance
their intelligence with neuroprosthetics (i.e. an “exocortex”):
https://ieeexplore.ieee.org/document/6893912
The people who rule
over us are Dark Triad types who cannot be trusted with such power:
https://www.sakkyndig.com/psykologi/artvit/babiak2010.pdf
https://fortune.com/2021/06/06/corporate-psychopaths-business-leadership-csr/
https://www.forbes.com/sites/jackmccullough/2019/12/09/the-psychopathic-ceo/
https://en.wikipedia.org/wiki/Psychopathy_in_the_workplace
END