This under no circumstances can any longer be allowed to go unmentioned. (Not using the 'S' word since it will likely get even this little site flagged or worse.) Currently what you are about to read is being scrubbed from absolutely every place and platform that posts it. Let's see how we do.
The Fightback is beginning, my friends, and from where I sit, this is the No.1 ordnance out there so far, posted by an anon "mystery" man that possesses a wealth of knowledge particular to the scientific, medical, and epidemiological fields, to say nothing of the overall 'parapolitical' milieu.
Read this closely, and in particular notice the name drops towards the end of the document and who they connect back to (Lieber straight back to Epstein and that network for instance**)
It becomes very clear why no one culpable wants you to ever see this and are doing everything in their power to disappear it ASAP.
Much more "me" to come next time; working on lots for you guys, but for now, this little Night Gallery is proud to present "The Document."
** Lieber was also spectacularly funded by the DOD, DARPA, ONR, NIH, MITRE, and Epstein himself thru cutouts at Harvard. MITRE, for one, links to everything sketch imaginable, Much more on their sinister track record can be found here: http://mcmmadnessnews.blogspot.com/2016/02/dark-soul-of-new-machine.html and what it links to...
(The fact that the agendas of the World Economic Forum, MITRE, and Lieber -- and by extension, Epstein -- all seem to converge should be more than enough to give any rational, sane person pause.)
Spartacus
September 26, 2021
Posted by Raúl Ilargi Meijer at 12:28 pm Finance Tagged with: ACE2,
biowarfare, conspiracy, COVID, endothelial, isolation, neural lace, sepsis,
Spartacus, spike proteins, vaccines Add
comments
This is an anonymously posted document by someone who calls
themselves Spartacus. Because it’s anonymous, I can’t contact them to ask for
permission to publish. So I hesitated for a while, but it’s simply the best
document I’ve seen on Covid, vaccines, etc. Whoever Spartacus is, they have a
very elaborate knowledge in “the field”. If you want to know a lot more about
the no. 1 issue in the world today, read it. And don’t worry if you don’t
understand every single word, neither do I. But I learned a lot.
The original PDF doc is here: Covid19 – The Spartacus Letter
Hello,
My name is Spartacus, and I’ve had enough.
We have been forced to watch America and the Free World spin
into inexorable decline due to a biowarfare attack. We, along with countless
others, have been victimized and gaslit by propaganda and psychological warfare
operations being conducted by an unelected, unaccountable Elite against the American
people and our allies.
Our mental and physical health have suffered immensely over
the course of the past year and a half. We have felt the sting of isolation,
lockdown, masking, quarantines, and other completely nonsensical acts of
healthcare theater that have done absolutely nothing to protect the health or
wellbeing of the public from the ongoing COVID-19 pandemic.
Now, we are watching the medical establishment inject
literal poison into millions of our fellow Americans without so much as a fight.
We have been told that we will be fired and denied our
livelihoods if we refuse to vaccinate. This was the last straw.
We have spent thousands of hours analyzing leaked footage
from Wuhan, scientific papers from primary sources, as well as the paper trails
left by the medical establishment.
What we have discovered would shock anyone to their core.
First, we will summarize our findings, and then, we will
explain them in detail. References will be placed at the end.
Summary:
• COVID-19 is a blood and blood vessel disease. SARS-CoV-2
infects the lining of human blood vessels, causing them to leak into the lungs.
• Current treatment protocols (e.g. invasive ventilation)
are actively harmful to patients, accelerating oxidative stress and causing
severe VILI (ventilator-induced lung injuries). The continued use of
ventilators in the absence of any proven medical benefit constitutes mass
murder.
• Existing countermeasures are inadequate to slow the spread
of what is an aerosolized and potentially wastewater-borne virus, and
constitute a form of medical theater.
• Various non-vaccine interventions have been suppressed by
both the media and the medical establishment in favor of vaccines and expensive
patented drugs.
• The authorities have denied the usefulness of natural
immunity against COVID-19, despite the fact that natural immunity confers
protection against all of the virus’s proteins, and not just one.
• Vaccines will do more harm than good. The antigen that
these vaccines are based on, SARS-CoV- 2 Spike, is a toxic protein. SARS-CoV-2
may have ADE, or antibody-dependent enhancement; current antibodies may not
neutralize future strains, but instead help them infect immune cells. Also,
vaccinating during a pandemic with a leaky vaccine removes the evolutionary
pressure for a virus to become less lethal.
• There is a vast and appalling criminal conspiracy that
directly links both Anthony Fauci and Moderna to the Wuhan Institute of
Virology.
• COVID-19 vaccine researchers are directly linked to scientists
involved in brain-computer interface (“neural lace”) tech, one of whom was
indicted for taking grant money from China.
• Independent researchers have discovered mysterious
nanoparticles inside the vaccines that are not supposed to be present.
• The entire pandemic is being used as an excuse for a vast
political and economic transformation of Western society that will enrich the
already rich and turn the rest of us into serfs and untouchables.
COVID-19 Pathophysiology and Treatments:
COVID-19 is not a viral pneumonia. It is a viral vascular
endotheliitis and attacks the lining of blood vessels, particularly the small
pulmonary alveolar capillaries, leading to endothelial cell activation and
sloughing, coagulopathy, sepsis, pulmonary edema, and ARDS-like symptoms. This
is a disease of the blood and blood vessels. The circulatory system. Any
pneumonia that it causes is secondary to that.
In severe cases, this leads to sepsis, blood clots, and
multiple organ failure, including hypoxic and inflammatory damage to various
vital organs, such as the brain, heart, liver, pancreas, kidneys, and
intestines.
Some of the most common laboratory findings in COVID-19 are
elevated D-dimer, elevated prothrombin time, elevated C-reactive protein,
neutrophilia, lymphopenia, hypocalcemia, and hyperferritinemia, essentially
matching a profile of coagulopathy and immune system hyperactivation/immune
cell exhaustion.
COVID-19 can present as almost anything, due to the wide
tropism of SARS-CoV-2 for various tissues in the body’s vital organs. While its
most common initial presentation is respiratory illness and flu-like symptoms,
it can present as brain inflammation, gastrointestinal disease, or even heart
attack or pulmonary embolism.
COVID-19 is more severe in those with specific
comorbidities, such as obesity, diabetes, and hypertension. This is because
these conditions involve endothelial dysfunction, which renders the circulatory
system more susceptible to infection and injury by this particular virus.
The vast majority of COVID-19 cases are mild and do not
cause significant disease. In known cases, there is something known as the
80/20 rule, where 80% of cases are mild and 20% are severe or critical.
However, this ratio is only correct for known cases, not all infections. The
number of actual infections is much, much higher. Consequently, the mortality
and morbidity rate is lower. However, COVID-19 spreads very quickly, meaning
that there are a significant number of severely-ill and critically-ill patients
appearing in a short time frame.
In those who have critical COVID-19-induced sepsis, hypoxia,
coagulopathy, and ARDS, the most common treatments are intubation, injected
corticosteroids, and blood thinners. This is not the correct treatment for
COVID-19. In severe hypoxia, cellular metabolic shifts cause ATP to break down
into hypoxanthine, which, upon the reintroduction of oxygen, causes xanthine
oxidase to produce tons of highly damaging radicals that attack tissue. This is
called ischemia-reperfusion injury, and it’s why the majority of people who go
on a ventilator are dying. In the mitochondria, succinate buildup due to sepsis
does the same exact thing; when oxygen is reintroduced, it makes superoxide
radicals. Make no mistake, intubation will kill people who have COVID-19.
The end-stage of COVID-19 is severe lipid peroxidation,
where fats in the body start to “rust” due to damage by oxidative stress. This
drives autoimmunity. Oxidized lipids appear as foreign objects to the immune
system, which recognizes and forms antibodies against OSEs, or
oxidation-specific epitopes. Also, oxidized lipids feed directly into pattern
recognition receptors, triggering even more inflammation and summoning even
more cells of the innate immune system that release even more destructive
enzymes. This is similar to the pathophysiology of Lupus.
COVID-19’s pathology is dominated by extreme oxidative
stress and neutrophil respiratory burst, to the point where hemoglobin becomes
incapable of carrying oxygen due to heme iron being stripped out of heme by
hypochlorous acid. No amount of supplemental oxygen can oxygenate blood that
chemically refuses to bind O2.
The breakdown of the pathology is as follows:
SARS-CoV-2 Spike binds to ACE2. Angiotensin Converting
Enzyme 2 is an enzyme that is part of the renin-angiotensin-aldosterone system,
or RAAS. The RAAS is a hormone control system that moderates fluid volume in
the body and in the bloodstream (i.e. osmolarity) by controlling salt retention
and excretion. This protein, ACE2, is ubiquitous in every part of the body that
interfaces with the circulatory system, particularly in vascular endothelial
cells and pericytes, brain astrocytes, renal tubules and podocytes, pancreatic
islet cells, bile duct and intestinal epithelial cells, and the seminiferous
ducts of the testis, all of which SARS-CoV-2 can infect, not just the lungs.
SARS-CoV-2 infects a cell as follows: SARS-CoV-2 Spike
undergoes a conformational change where the S1 trimers flip up and extend,
locking onto ACE2 bound to the surface of a cell. TMPRSS2, or transmembrane
protease serine 2, comes along and cuts off the heads of the Spike, exposing
the S2 stalk-shaped subunit inside. The remainder of the Spike undergoes a
conformational change that causes it to unfold like an extension ladder,
embedding itself in the cell membrane. Then, it folds back upon itself, pulling
the viral membrane and the cell membrane together. The two membranes fuse, with
the virus’s proteins migrating out onto the surface of the cell. The SARS-CoV-2
nucleocapsid enters the cell, disgorging its genetic material and beginning the
viral replication process, hijacking the cell’s own structures to produce more
virus.
SARS-CoV-2 Spike proteins embedded in a cell can actually
cause human cells to fuse together, forming syncytia/MGCs (multinuclear giant
cells). They also have other pathogenic, harmful effects. SARS-CoV- 2’s
viroporins, such as its Envelope protein, act as calcium ion channels,
introducing calcium into infected cells. The virus suppresses the natural
interferon response, resulting in delayed inflammation. SARS-CoV-2 N protein
can also directly activate the NLRP3 inflammasome. Also, it suppresses the Nrf2
antioxidant pathway. The suppression of ACE2 by binding with Spike causes a
buildup of bradykinin that would otherwise be broken down by ACE2.
This constant calcium influx into the cells results in (or
is accompanied by) noticeable hypocalcemia, or low blood calcium, especially in
people with Vitamin D deficiencies and pre-existing endothelial dysfunction.
Bradykinin upregulates cAMP, cGMP, COX, and Phospholipase C activity. This
results in prostaglandin release and vastly increased intracellular calcium
signaling, which promotes highly aggressive ROS release and ATP depletion.
NADPH oxidase releases superoxide into the extracellular space. Superoxide
radicals react with nitric oxide to form peroxynitrite. Peroxynitrite reacts
with the tetrahydrobiopterin cofactor needed by endothelial nitric oxide
synthase, destroying it and “uncoupling” the enzymes, causing nitric oxide
synthase to synthesize more superoxide instead. This proceeds in a positive
feedback loop until nitric oxide bioavailability in the circulatory system is
depleted.
Dissolved nitric oxide gas produced constantly by eNOS
serves many important functions, but it is also antiviral against SARS-like
coronaviruses, preventing the palmitoylation of the viral Spike protein and
making it harder for it to bind to host receptors. The loss of NO allows the
virus to begin replicating with impunity in the body. Those with endothelial
dysfunction (i.e. hypertension, diabetes, obesity, old age, African-American
race) have redox equilibrium issues to begin with, giving the virus an
advantage.
Due to the extreme cytokine release triggered by these
processes, the body summons a great deal of neutrophils and monocyte-derived
alveolar macrophages to the lungs. Cells of the innate immune system are the
first-line defenders against pathogens. They work by engulfing invaders and
trying to attack them with enzymes that produce powerful oxidants, like SOD and
MPO. Superoxide dismutase takes superoxide and makes hydrogen peroxide, and
myeloperoxidase takes hydrogen peroxide and chlorine ions and makes
hypochlorous acid, which is many, many times more reactive than sodium
hypochlorite bleach.
Neutrophils have a nasty trick. They can also eject these
enzymes into the extracellular space, where they will continuously spit out
peroxide and bleach into the bloodstream. This is called neutrophil
extracellular trap formation, or, when it becomes pathogenic and
counterproductive, NETosis. In severe and critical COVID-19, there is actually
rather severe NETosis.
Hypochlorous acid building up in the bloodstream begins to
bleach the iron out of heme and compete for O2 binding sites. Red blood cells
lose the ability to transport oxygen, causing the sufferer to turn blue in the
face. Unliganded iron, hydrogen peroxide, and superoxide in the bloodstream
undergo the Haber- Weiss and Fenton reactions, producing extremely reactive
hydroxyl radicals that violently strip electrons from surrounding fats and DNA,
oxidizing them severely.
This condition is not unknown to medical science. The actual
name for all of this is acute sepsis.
We know this is happening in COVID-19 because people who
have died of the disease have noticeable ferroptosis signatures in their
tissues, as well as various other oxidative stress markers such as nitrotyrosine,
4-HNE, and malondialdehyde.
When you intubate someone with this condition, you are
setting off a free radical bomb by supplying the cells with O2. It’s a
catch-22, because we need oxygen to make Adenosine Triphosphate (that is, to
live), but O2 is also the precursor of all these damaging radicals that lead to
lipid peroxidation.
The correct treatment for severe COVID-19 related sepsis is
non-invasive ventilation, steroids, and antioxidant infusions. Most of the
drugs repurposed for COVID-19 that show any benefit whatsoever in rescuing
critically-ill COVID-19 patients are antioxidants. N-acetylcysteine, melatonin,
fluvoxamine, budesonide, famotidine, cimetidine, and ranitidine are all
antioxidants. Indomethacin prevents iron- driven oxidation of arachidonic acid
to isoprostanes. There are powerful antioxidants such as apocynin that have not
even been tested on COVID-19 patients yet which could defang neutrophils,
prevent lipid peroxidation, restore endothelial health, and restore oxygenation
to the tissues.
Scientists who know anything about pulmonary neutrophilia,
ARDS, and redox biology have known or surmised much of this since March 2020.
In April 2020, Swiss scientists confirmed that COVID-19 was a vascular
endotheliitis. By late 2020, experts had already concluded that COVID-19 causes
a form of viral sepsis. They also know that sepsis can be effectively treated
with antioxidants. None of this information is particularly new, and yet, for
the most part, it has not been acted upon. Doctors continue to use damaging
intubation techniques with high PEEP settings despite high lung compliance and
poor oxygenation, killing an untold number of critically ill patients with
medical malpractice.
Because of the way they are constructed, Randomized Control
Trials will never show any benefit for any antiviral against COVID-19. Not
Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The reason for this is
simple; for the patients that they have recruited for these studies, such as
Oxford’s ludicrous RECOVERY study, the intervention is too late to have any
positive effect.
The clinical course of COVID-19 is such that by the time
most people seek medical attention for hypoxia, their viral load has already
tapered off to almost nothing. If someone is about 10 days post-exposure and
has already been symptomatic for five days, there is hardly any virus left in
their bodies, only cellular damage and derangement that has initiated a
hyperinflammatory response. It is from this group that the clinical trials for
antivirals have recruited, pretty much exclusively.
In these trials, they give antivirals to severely ill
patients who have no virus in their bodies, only a delayed hyperinflammatory
response, and then absurdly claim that antivirals have no utility in treating
or preventing COVID-19. These clinical trials do not recruit people who are
pre-symptomatic. They do not test pre-exposure or post-exposure prophylaxis.
This is like using a defibrillator to shock only flatline,
and then absurdly claiming that defibrillators have no medical utility
whatsoever when the patients refuse to rise from the dead. The intervention is
too late. These trials for antivirals show systematic, egregious selection
bias. They are providing a treatment that is futile to the specific cohort they
are enrolling.
India went against the instructions of the WHO and mandated
the prophylactic usage of Ivermectin. They have almost completely eradicated
COVID-19. The Indian Bar Association of Mumbai has brought criminal charges
against WHO Chief Scientist Dr. Soumya Swaminathan for recommending against the
use of Ivermectin.
Ivermectin is not “horse dewormer”. Yes, it is sold in
veterinary paste form as a dewormer for animals. It has also been available in
pill form for humans for decades, as an antiparasitic drug.
The media have disingenuously claimed that because
Ivermectin is an antiparasitic drug, it has no utility as an antivirus. This is
incorrect. Ivermectin has utility as an antiviral. It blocks importin,
preventing nuclear import, effectively inhibiting viral access to cell nuclei.
Many drugs currently on the market have multiple modes of action. Ivermectin is
one such drug. It is both antiparasitic and antiviral.
In Bangladesh, Ivermectin costs $1.80 for an entire 5-day
course. Remdesivir, which is toxic to the liver, costs $3,120 for a 5-day
course of the drug. Billions of dollars of utterly useless Remdesivir were sold
to our governments on the taxpayer’s dime, and it ended up being totally
useless for treating hyperinflammatory COVID-19. The media has hardly even
covered this at all.
The opposition to the use of generic Ivermectin is not based
in science. It is purely financially and politically-motivated. An effective
non-vaccine intervention would jeopardize the rushed FDA approval of patented
vaccines and medicines for which the pharmaceutical industry stands to rake in
billions upon billions of dollars in sales on an ongoing basis.
The majority of the public are scientifically illiterate and
cannot grasp what any of this even means, thanks to a pathetic educational
system that has miseducated them. You would be lucky to find 1 in 100 people
who have even the faintest clue what any of this actually means.
COVID-19 Transmission:
COVID-19 is airborne. The WHO carried water for China by
claiming that the virus was only droplet- borne. Our own CDC absurdly claimed
that it was mostly transmitted by fomite-to-face contact, which, given its
rapid spread from Wuhan to the rest of the world, would have been physically
impossible.
The ridiculous belief in fomite-to-face being a primary mode
of transmission led to the use of surface disinfection protocols that wasted
time, energy, productivity, and disinfectant.
The 6-foot guidelines are absolutely useless. The minimum
safe distance to protect oneself from an aerosolized virus is to be 15+ feet
away from an infected person, no closer. Realistically, no public transit is
safe.
Surgical masks do not protect you from aerosols. The virus
is too small and the filter media has too large of gaps to filter it out. They
may catch respiratory droplets and keep the virus from being expelled by
someone who is sick, but they do not filter a cloud of infectious aerosols if
someone were to walk into said cloud.
The minimum level of protection against this virus is quite
literally a P100 respirator, a PAPR/CAPR, or a 40mm NATO CBRN respirator,
ideally paired with a full-body tyvek or tychem suit, gloves, and booties, with
all the holes and gaps taped.
Live SARS-CoV-2 may potentially be detected in sewage
outflows, and there may be oral-fecal transmission. During the SARS outbreak in
2003, in the Amoy Gardens incident, hundreds of people were infected by
aerosolized fecal matter rising from floor drains in their apartments.
COVID-19 Vaccine Dangers:
The vaccines for COVID-19 are not sterilizing and do not
prevent infection or transmission. They are “leaky” vaccines. This means they
remove the evolutionary pressure on the virus to become less lethal. It also
means that the vaccinated are perfect carriers. In other words, those who are
vaccinated are a threat to the unvaccinated, not the other way around.
All of the COVID-19 vaccines currently in use have undergone
minimal testing, with highly accelerated clinical trials. Though they appear to
limit severe illness, the long-term safety profile of these vaccines remains
unknown.
Some of these so-called “vaccines” utilize an untested new
technology that has never been used in vaccines before. Traditional vaccines
use weakened or killed virus to stimulate an immune response. The Moderna and
Pfizer-BioNTech vaccines do not. They are purported to consist of an
intramuscular shot containing a suspension of lipid nanoparticles filled with
messenger RNA. The way they generate an immune response is by fusing with cells
in a vaccine recipient’s shoulder, undergoing endocytosis, releasing their mRNA
cargo into those cells, and then utilizing the ribosomes in those cells to
synthesize modified SARS-CoV-2 Spike proteins in-situ.
These modified Spike proteins then migrate to the surface of
the cell, where they are anchored in place by a transmembrane domain. The
adaptive immune system detects the non-human viral protein being expressed by
these cells, and then forms antibodies against that protein. This is purported
to confer protection against the virus, by training the adaptive immune system
to recognize and produce antibodies against the Spike on the actual virus. The
J&J and AstraZeneca vaccines do something similar, but use an adenovirus
vector for genetic material delivery instead of a lipid nanoparticle. These
vaccines were produced or validated with the aid of fetal cell lines HEK-293
and PER.C6, which people with certain religious convictions may object strongly
to.
SARS-CoV-2 Spike is a highly pathogenic protein on its own.
It is impossible to overstate the danger presented by introducing this protein
into the human body.
It is claimed by vaccine manufacturers that the vaccine
remains in cells in the shoulder, and that SARS- CoV-2 Spike produced and
expressed by these cells from the vaccine’s genetic material is harmless and
inert, thanks to the insertion of prolines in the Spike sequence to stabilize
it in the prefusion conformation, preventing the Spike from becoming active and
fusing with other cells. However, a pharmacokinetic study from Japan showed
that the lipid nanoparticles and mRNA from the Pfizer vaccine did not stay in
the shoulder, and in fact bioaccumulated in many different organs, including
the reproductive organs and adrenal glands, meaning that modified Spike is
being expressed quite literally all over the place. These lipid nanoparticles
may trigger anaphylaxis in an unlucky few, but far more concerning is the
unregulated expression of Spike in various somatic cell lines far from the
injection site and the unknown consequences of that.
Messenger RNA is normally consumed right after it is
produced in the body, being translated into a protein by a ribosome. COVID-19
vaccine mRNA is produced outside the body, long before a ribosome translates
it. In the meantime, it could accumulate damage if inadequately preserved. When
a ribosome attempts to translate a damaged strand of mRNA, it can become
stalled. When this happens, the ribosome becomes useless for translating
proteins because it now has a piece of mRNA stuck in it, like a lace card in an
old punch card reader. The whole thing has to be cleaned up and new ribosomes
synthesized to replace it. In cells with low ribosome turnover, like nerve
cells, this can lead to reduced protein synthesis, cytopathic effects, and
neuropathies.
Certain proteins, including SARS-CoV-2 Spike, have
proteolytic cleavage sites that are basically like little dotted lines that say
“cut here”, which attract a living organism’s own proteases (essentially, molecular
scissors) to cut them. There is a possibility that S1 may be proteolytically
cleaved from S2, causing active S1 to float away into the bloodstream while
leaving the S2 “stalk” embedded in the membrane of the cell that expressed the
protein.
SARS-CoV-2 Spike has a Superantigenic region (SAg), which
may promote extreme inflammation.
Anti-Spike antibodies were found in one study to function as
autoantibodies and attack the body’s own cells. Those who have been immunized
with COVID-19 vaccines have developed blood clots, myocarditis, Guillain-Barre
Syndrome, Bell’s Palsy, and multiple sclerosis flares, indicating that the
vaccine promotes autoimmune reactions against healthy tissue.
SARS-CoV-2 Spike does not only bind to ACE2. It was
suspected to have regions that bind to basigin, integrins, neuropilin-1, and
bacterial lipopolysaccharides as well. SARS-CoV-2 Spike, on its own, can
potentially bind any of these things and act as a ligand for them, triggering
unspecified and likely highly inflammatory cellular activity.
SARS-CoV-2 Spike contains an unusual PRRA insert that forms
a furin cleavage site. Furin is a ubiquitous human protease, making this an
ideal property for the Spike to have, giving it a high degree of cell tropism.
No wild-type SARS-like coronaviruses related to SARS-CoV-2 possess this
feature, making it highly suspicious, and perhaps a sign of human tampering.
SARS-CoV-2 Spike has a prion-like domain that enhances its
infectiousness.
The Spike S1 RBD may bind to heparin-binding proteins and
promote amyloid aggregation. In humans, this could lead to Parkinson’s, Lewy
Body Dementia, premature Alzheimer’s, or various other neurodegenerative
diseases. This is very concerning because SARS-CoV-2 S1 is capable of injuring
and penetrating the blood-brain barrier and entering the brain. It is also
capable of increasing the permeability of the blood-brain barrier to other
molecules.
SARS-CoV-2, like other betacoronaviruses, may have
Dengue-like ADE, or antibody-dependent enhancement of disease. For those who
aren’t aware, some viruses, including betacoronaviruses, have a feature called
ADE. There is also something called Original Antigenic Sin, which is the
observation that the body prefers to produce antibodies based on
previously-encountered strains of a virus over newly- encountered ones.
In ADE, antibodies from a previous infection become
non-neutralizing due to mutations in the virus’s proteins. These
non-neutralizing antibodies then act as trojan horses, allowing live, active
virus to be pulled into macrophages through their Fc receptor pathways,
allowing the virus to infect immune cells that it would not have been able to
infect before. This has been known to happen with Dengue Fever; when someone
gets sick with Dengue, recovers, and then contracts a different strain, they
can get very, very ill.
If someone is vaccinated with mRNA based on the Spike from
the initial Wuhan strain of SARS-CoV-2, and then they become infected with a
future, mutated strain of the virus, they may become severely ill. In other
words, it is possible for vaccines to sensitize someone to disease.
There is a precedent for this in recent history. Sanofi’s
Dengvaxia vaccine for Dengue failed because it caused immune sensitization in
people whose immune systems were Dengue-naive.
In mice immunized against SARS-CoV and challenged with the
virus, a close relative of SARS-CoV-2, they developed immune sensitization, Th2
immunopathology, and eosinophil infiltration in their lungs.
We have been told that SARS-CoV-2 mRNA vaccines cannot be
integrated into the human genome, because messenger RNA cannot be turned back
into DNA. This is false. There are elements in human cells called LINE-1
retrotransposons, which can indeed integrate mRNA into a human genome by
endogenous reverse transcription. Because the mRNA used in the vaccines is
stabilized, it hangs around in cells longer, increasing the chances for this to
happen. If the gene for SARS-CoV-2 Spike is integrated into a portion of the
genome that is not silent and actually expresses a protein, it is possible that
people who take this vaccine may continuously express SARS-CoV-2 Spike from
their somatic cells for the rest of their lives.
By inoculating people with a vaccine that causes their
bodies to produce Spike in-situ, they are being inoculated with a pathogenic
protein. A toxin that may cause long-term inflammation, heart problems, and a
raised risk of cancers. In the long-term, it may also potentially lead to
premature neurodegenerative disease.
Absolutely nobody should be compelled to take this vaccine
under any circumstances, and in actual fact, the vaccination campaign must be
stopped immediately.
COVID-19 Criminal Conspiracy:
The vaccine and the virus were made by the same people.
In 2014, there was a moratorium on SARS gain-of-function
research that lasted until 2017. This research was not halted. Instead, it was
outsourced, with the federal grants being laundered through NGOs.
Ralph Baric is a virologist and SARS expert at UNC Chapel
Hill in North Carolina. This is who Anthony Fauci was referring to when he
insisted, before Congress, that if any gain-of-function research was being
conducted, it was being conducted in North Carolina.
This was a lie. Anthony Fauci lied before Congress. A
felony.
Ralph Baric and Shi Zhengli are colleagues and have
co-written papers together. Ralph Baric mentored Shi Zhengli in his
gain-of-function manipulation techniques, particularly serial passage, which
results in a virus that appears as if it originated naturally. In other words,
deniable bioweapons. Serial passage in humanized hACE2 mice may have produced
something like SARS-CoV-2.
The funding for the gain-of-function research being
conducted at the Wuhan Institute of Virology came from Peter Daszak. Peter
Daszak runs an NGO called EcoHealth Alliance. EcoHealth Alliance received
millions of dollars in grant money from the National Institutes of
Health/National Institute of Allergy and Infectious Diseases (that is, Anthony
Fauci), the Defense Threat Reduction Agency (part of the US Department of
Defense), and the United States Agency for International Development. NIH/NIAID
contributed a few million dollars, and DTRA and USAID each contributed tens of
millions of dollars towards this research. Altogether, it was over a hundred
million dollars.
EcoHealth Alliance subcontracted these grants to the Wuhan
Institute of Virology, a lab in China with a very questionable safety record
and poorly trained staff, so that they could conduct gain-of-function research,
not in their fancy P4 lab, but in a level-2 lab where technicians wore nothing
more sophisticated than perhaps a hairnet, latex gloves, and a surgical mask,
instead of the bubble suits used when working with dangerous viruses. Chinese
scientists in Wuhan reported being routinely bitten and urinated on by
laboratory animals. Why anyone would outsource this dangerous and delicate work
to the People’s Republic of China, a country infamous for industrial accidents
and massive explosions that have claimed hundreds of lives, is completely
beyond me, unless the aim was to start a pandemic on purpose.
In November of 2019, three technicians at the Wuhan
Institute of Virology developed symptoms consistent with a flu-like illness. Anthony
Fauci, Peter Daszak, and Ralph Baric knew at once what had happened, because
back channels exist between this laboratory and our scientists and officials.
December 12th, 2019, Ralph Baric signed a Material Transfer
Agreement (essentially, an NDA) to receive Coronavirus mRNA vaccine-related
materials co-owned by Moderna and NIH. It wasn’t until a whole month later, on
January 11th, 2020, that China allegedly sent us the sequence to what would
become known as SARS-CoV-2. Moderna claims, rather absurdly, that they
developed a working vaccine from this sequence in under 48 hours.
Stephane Bancel, the current CEO of Moderna, was formerly
the CEO of bioMerieux, a French multinational corporation specializing in
medical diagnostic tech, founded by one Alain Merieux. Alain Merieux was one of
the individuals who was instrumental in the construction of the Wuhan Institute
of Virology’s P4 lab.
The sequence given as the closest relative to SARS-CoV-2,
RaTG13, is not a real virus. It is a forgery. It was made by entering a gene
sequence by hand into a database, to create a cover story for the existence of
SARS-CoV-2, which is very likely a gain-of-function chimera produced at the
Wuhan Institute of Virology and was either leaked by accident or intentionally
released.
The animal reservoir of SARS-CoV-2 has never been found.
This is not a conspiracy “theory”. It is an actual criminal
conspiracy, in which people connected to the development of Moderna’s mRNA-1273
are directly connected to the Wuhan Institute of Virology and their
gain-of-function research by very few degrees of separation, if any. The paper
trail is well- established.
The lab-leak theory has been suppressed because pulling that
thread leads one to inevitably conclude that there is enough circumstantial
evidence to link Moderna, the NIH, the WIV, and both the vaccine and the
virus’s creation together. In a sane country, this would have immediately led
to the world’s biggest RICO and mass murder case. Anthony Fauci, Peter Daszak,
Ralph Baric, Shi Zhengli, and Stephane Bancel, and their accomplices, would
have been indicted and prosecuted to the fullest extent of the law. Instead,
billions of our tax dollars were awarded to the perpetrators.
The FBI raided Allure Medical in Shelby Township north of Detroit
for billing insurance for “fraudulent COVID-19 cures”. The treatment they were
using? Intravenous Vitamin C. An antioxidant. Which, as described above, is an
entirely valid treatment for COVID-19-induced sepsis, and indeed, is now part
of the MATH+ protocol advanced by Dr. Paul E. Marik.
The FDA banned ranitidine (Zantac) due to supposed NDMA
(N-nitrosodimethylamine) contamination. Ranitidine is not only an H2 blocker
used as antacid, but also has a powerful antioxidant effect, scavenging
hydroxyl radicals. This gives it utility in treating COVID-19.
The FDA also attempted to take N-acetylcysteine, a harmless
amino acid supplement and antioxidant, off the shelves, compelling Amazon to
remove it from their online storefront.
This leaves us with a chilling question: did the FDA
knowingly suppress antioxidants useful for treating COVID-19 sepsis as part of
a criminal conspiracy against the American public?
The establishment is cooperating with, and facilitating, the
worst criminals in human history, and are actively suppressing non-vaccine
treatments and therapies in order to compel us to inject these criminals’
products into our bodies. This is absolutely unacceptable.
COVID-19 Vaccine Development and Links to Transhumanism:
This section deals with some more speculative aspects of the
pandemic and the medical and scientific establishment’s reaction to it, as well
as the disturbing links between scientists involved in vaccine research and
scientists whose work involved merging nanotechnology with living cells.
On June 9th, 2020, Charles Lieber, a Harvard nanotechnology
researcher with decades of experience, was indicted by the DOJ for fraud.
Charles Lieber received millions of dollars in grant money from the US
Department of Defense, specifically the military think tanks DARPA, AFOSR, and
ONR, as well as NIH and MITRE. His specialty is the use of silicon nanowires in
lieu of patch clamp electrodes to monitor and modulate intracellular activity,
something he has been working on at Harvard for the past twenty years. He was
claimed to have been working on silicon nanowire batteries in China, but none
of his colleagues can recall him ever having worked on battery technology in
his life; all of his research deals with bionanotechnology, or the blending of
nanotech with living cells.
The indictment was over his collaboration with the Wuhan
University of Technology. He had double- dipped, against the terms of his DOD
grants, and taken money from the PRC’s Thousand Talents plan, a program which
the Chinese government uses to bribe Western scientists into sharing
proprietary R&D information that can be exploited by the PLA for strategic
advantage.
Charles Lieber’s own papers describe the use of silicon
nanowires for brain-computer interfaces, or “neural lace” technology. His
papers describe how neurons can endocytose whole silicon nanowires or parts of
them, monitoring and even modulating neuronal activity.
Charles Lieber was a colleague of Robert Langer. Together,
along with Daniel S. Kohane, they worked on a paper describing artificial
tissue scaffolds that could be implanted in a human heart to monitor its
activity remotely.
Robert Langer, an MIT alumnus and expert in nanotech drug
delivery, is one of the co-founders of Moderna. His net worth is now $5.1
billion USD thanks to Moderna’s mRNA-1273 vaccine sales.
Both Charles Lieber and Robert Langer’s bibliographies
describe, essentially, techniques for human enhancement, i.e. transhumanism.
Klaus Schwab, the founder of the World Economic Forum and the architect behind
the so-called “Great Reset”, has long spoken of the “blending of biology and
machinery” in his books.
Since these revelations, it has come to the attention of
independent researchers that the COVID-19 vaccines may contain reduced graphene
oxide nanoparticles. Japanese researchers have also found unexplained
contaminants in COVID-19 vaccines.
Graphene oxide is an anxiolytic. It has been shown to reduce
the anxiety of laboratory mice when injected into their brains. Indeed, given
SARS-CoV-2 Spike’s propensity to compromise the blood-brain barrier and
increase its permeability, it is the perfect protein for preparing brain tissue
for extravasation of nanoparticles from the bloodstream and into the brain.
Graphene is also highly conductive and, in some circumstances, paramagnetic.
In 2013, under the Obama administration, DARPA launched the
BRAIN Initiative; BRAIN is an acronym for Brain Research Through Advancing
Innovative Neurotechnologies®. This program involves the development of brain-computer
interface technologies for the military, particularly non-invasive, injectable
systems that cause minimal damage to brain tissue when removed. Supposedly,
this technology would be used for healing wounded soldiers with traumatic brain
injuries, the direct brain control of prosthetic limbs, and even new abilities
such as controlling drones with one’s mind.
Various methods have been proposed for achieving this,
including optogenetics, magnetogenetics, ultrasound, implanted electrodes, and
transcranial electromagnetic stimulation. In all instances, the goal is to
obtain read or read-write capability over neurons, either by stimulating and
probing them, or by rendering them especially sensitive to stimulation and
probing.
However, the notion of the widespread use of BCI technology,
such as Elon Musk’s Neuralink device, raises many concerns over privacy and
personal autonomy. Reading from neurons is problematic enough on its own.
Wireless brain-computer interfaces may interact with current or future wireless
GSM infrastructure, creating neurological data security concerns. A hacker or
other malicious actor may compromise such networks to obtain people’s brain
data, and then exploit it for nefarious purposes.
However, a device capable of writing to human neurons, not
just reading from them, presents another, even more serious set of ethical
concerns. A BCI that is capable of altering the contents of one’s mind for
innocuous purposes, such as projecting a heads-up display onto their brain’s
visual center or sending audio into one’s auditory cortex, would also
theoretically be capable of altering mood and personality, or perhaps even
subjugating someone’s very will, rendering them utterly obedient to authority.
This technology would be a tyrant’s wet dream. Imagine soldiers who would shoot
their own countrymen without hesitation, or helpless serfs who are satisfied to
live in literal dog kennels.
BCIs could be used to unscrupulously alter perceptions of
basic things such as emotions and values, changing people’s thresholds of
satiety, happiness, anger, disgust, and so forth. This is not inconsequential.
Someone’s entire regime of behaviors could be altered by a BCI, including such
things as suppressing their appetite or desire for virtually anything on Maslow’s
Hierarchy of Needs.
Anything is possible when you have direct access to
someone’s brain and its contents. Someone who is obese could be made to feel
disgust at the sight of food. Someone who is involuntarily celibate could have
their libido disabled so they don’t even desire sex to begin with. Someone who
is racist could be forced to feel delight over cohabiting with people of other
races. Someone who is violent could be forced to be meek and submissive. These
things might sound good to you if you are a tyrant, but to normal people, the
idea of personal autonomy being overridden to such a degree is appalling.
For the wealthy, neural laces would be an unequaled boon,
giving them the opportunity to enhance their intelligence with neuroprosthetics
(i.e. an “exocortex”), and to deliver irresistible commands directly into the
minds of their BCI-augmented servants, even physically or sexually abusive
commands that they would normally refuse.
If the vaccine is a method to surreptitiously introduce an
injectable BCI into millions of people without their knowledge or consent, then
what we are witnessing is the rise of a tyrannical regime unlike anything ever
seen before on the face of this planet, one that fully intends to strip every
man, woman, and child of our free will.
Our flaws are what make us human. A utopia arrived at by
removing people’s free will is not a utopia at all. It is a monomaniacal
nightmare. Furthermore, the people who rule over us are Dark Triad types who
cannot be trusted with such power. Imagine being beaten and sexually assaulted
by a wealthy and powerful psychopath and being forced to smile and laugh over
it because your neural lace gives you no choice but to obey your master.
The Elites are forging ahead with this technology without
giving people any room to question the social or ethical ramifications, or to
establish regulatory frameworks that ensure that our personal agency and
autonomy will not be overridden by these devices. They do this because they
secretly dream of a future where they can treat you worse than an animal and
you cannot even fight back. If this evil plan is allowed to continue, it will
spell the end of humanity as we know it.
Conclusions:
The current pandemic was produced and perpetuated by the
establishment, through the use of a virus engineered in a PLA-connected Chinese
biowarfare laboratory, with the aid of American taxpayer dollars and French
expertise.
This research was conducted under the absolutely ridiculous
euphemism of “gain-of-function” research, which is supposedly carried out in
order to determine which viruses have the highest potential for zoonotic
spillover and preemptively vaccinate or guard against them.
Gain-of-function/gain-of-threat research, a.k.a. “Dual-Use
Research of Concern”, or DURC, is bioweapon research by another,
friendlier-sounding name, simply to avoid the taboo of calling it what it
actually is. It has always been bioweapon research. The people who are
conducting this research fully understand that they are taking wild pathogens
that are not infectious in humans and making them more infectious, often taking
grants from military think tanks encouraging them to do so.
These virologists conducting this type of research are
enemies of their fellow man, like pyromaniac firefighters. GOF research has
never protected anyone from any pandemic. In fact, it has now started one,
meaning its utility for preventing pandemics is actually negative. It should
have been banned globally, and the lunatics performing it should have been put
in straitjackets long ago.
Either through a leak or an intentional release from the
Wuhan Institute of Virology, a deadly SARS strain is now endemic across the
globe, after the WHO and CDC and public officials first downplayed the risks,
and then intentionally incited a panic and lockdowns that jeopardized people’s
health and their livelihoods.
This was then used by the utterly depraved and psychopathic
aristocratic class who rule over us as an excuse to coerce people into
accepting an injected poison which may be a depopulation agent, a mind
control/pacification agent in the form of injectable “smart dust”, or both in
one. They believe they can get away with this by weaponizing the social stigma
of vaccine refusal. They are incorrect.
Their motives are clear and obvious to anyone who has been
paying attention. These megalomaniacs have raided the pension funds of the free
world. Wall Street is insolvent and has had an ongoing liquidity crisis since
the end of 2019. The aim now is to exert total, full-spectrum physical, mental,
and financial control over humanity before we realize just how badly we’ve been
extorted by these maniacs.
The pandemic and its response served multiple purposes for
the Elite:
• Concealing a depression brought on by the usurious plunder
of our economies conducted by rentier-capitalists and absentee owners who
produce absolutely nothing of any value to society whatsoever. Instead of us
having a very predictable Occupy Wall Street Part II, the Elites and their
stooges got to stand up on television and paint themselves as wise and
all-powerful saviors instead of the marauding cabal of despicable land pirates
that they are.
• Destroying small businesses and eroding the middle class.
• Transferring trillions of dollars of wealth from the
American public and into the pockets of billionaires and special interests.
• Engaging in insider trading, buying stock in biotech
companies and shorting brick-and-mortar businesses and travel companies, with
the aim of collapsing face-to-face commerce and tourism and replacing it with
e-commerce and servitization.
• Creating a casus belli for war with China, encouraging us
to attack them, wasting American lives and treasure and driving us to the brink
of nuclear armageddon.
• Establishing technological and biosecurity frameworks for
population control and technocratic- socialist “smart cities” where everyone’s
movements are despotically tracked, all in anticipation of widespread
automation, joblessness, and food shortages, by using the false guise of a
vaccine to compel cooperation.
Any one of these things would constitute a vicious rape of
Western society. Taken together, they beggar belief; they are a complete
inversion of our most treasured values.
What is the purpose of all of this? One can only speculate
as to the perpetrators’ motives, however, we have some theories.
The Elites are trying to pull up the ladder, erase upward
mobility for large segments of the population, cull political opponents and
other “undesirables”, and put the remainder of humanity on a tight leash,
rationing our access to certain goods and services that they have deemed
“high-impact”, such as automobile use, tourism, meat consumption, and so on.
Naturally, they will continue to have their own luxuries, as part of a strict
caste system akin to feudalism.
Why are they doing this? Simple. The Elites are
Neo-Malthusians and believe that we are overpopulated and that resource
depletion will collapse civilization in a matter of a few short decades. They
are not necessarily incorrect in this belief. We are overpopulated, and we are
consuming too many resources. However, orchestrating such a gruesome and
murderous power grab in response to a looming crisis demonstrates that they
have nothing but the utmost contempt for their fellow man.
To those who are participating in this disgusting farce
without any understanding of what they are doing, we have one word for you.
Stop. You are causing irreparable harm to your country and to your fellow
citizens.
To those who may be reading this warning and have full
knowledge and understanding of what they are doing and how it will unjustly
harm millions of innocent people, we have a few more words.
Damn you to hell. You will not destroy America and the Free World, and you will not have your New World Order. We will make certain of that.
'404' pdf proof copy with all references here: https://gateway.pinata.cloud/ipfs/QmVc3SibRH3VbMJv3x7BKCPfq43qyek2CP8ULnTV3E48V1
Much to digest. Take your time with this guys, and as always, please let me know what you think in the comments. Another batsignal was ready to go tonight, but I simply thought this was too important not to issue on its own as a standalone. Back soon, and One Love my brothers and sisters...
