Bitcoin Forum

Hello,
My name is Spartacus, and I’ve had enough.
We have been forced to watch America and the Free World spin into inexorable decline due to a
biowarfare attack. We, along with countless others, have been victimized and gaslit by propaganda and
psychological warfare operations being conducted by an unelected, unaccountable Elite against the
American people and our allies.
Our mental and physical health have suffered immensely over the course of the past year and a half. We
have felt the sting of isolation, lockdown, masking, quarantines, and other completely nonsensical acts
of healthcare theater that have done absolutely nothing to protect the health or wellbeing of the public
from the ongoing COVID-19 pandemic.
Now, we are watching the medical establishment inject literal poison into millions of our fellow
Americans without so much as a fight.
We have been told that we will be fired and denied our livelihoods if we refuse to vaccinate. This was
the last straw.
We have spent thousands of hours analyzing leaked footage from Wuhan, scientific papers from primary
sources, as well as the paper trails left by the medical establishment.
What we have discovered would shock anyone to their core.
First, we will summarize our findings, and then, we will explain them in detail. References will be placed
at the end.
Summary:
• COVID-19 is a blood and blood vessel disease. SARS-CoV-2 infects the lining of human blood
vessels, causing them to leak into the lungs.
• Current treatment protocols (e.g. invasive ventilation) are actively harmful to patients,
accelerating oxidative stress and causing severe VILI (ventilator-induced lung injuries). The
continued use of ventilators in the absence of any proven medical benefit constitutes mass
murder.
• Existing countermeasures are inadequate to slow the spread of what is an aerosolized and
potentially wastewater-borne virus, and constitute a form of medical theater.
• Various non-vaccine interventions have been suppressed by both the media and the medical
establishment in favor of vaccines and expensive patented drugs.
• The authorities have denied the usefulness of natural immunity against COVID-19, despite the
fact that natural immunity confers protection against all of the virus’s proteins, and not just one.
• Vaccines will do more harm than good. The antigen that these vaccines are based on, SARS-CoV2 Spike, is a toxic protein. SARS-CoV-2 may have ADE, or antibody-dependent enhancement;
current antibodies may not neutralize future strains, but instead help them infect immune cells.
Also, vaccinating during a pandemic with a leaky vaccine removes the evolutionary pressure for
a virus to become less lethal.
• There is a vast and appalling criminal conspiracy that directly links both Anthony Fauci and
Moderna to the Wuhan Institute of Virology.
• COVID-19 vaccine researchers are directly linked to scientists involved in brain-computer
interface (“neural lace”) tech, one of whom was indicted for taking grant money from China.
• Independent researchers have discovered mysterious nanoparticles inside the vaccines that are
not supposed to be present.
• The entire pandemic is being used as an excuse for a vast political and economic transformation
of Western society that will enrich the already rich and turn the rest of us into serfs and
untouchables.
COVID-19 Pathophysiology and Treatments:
COVID-19 is not a viral pneumonia. It is a viral vascular endotheliitis and attacks the lining of blood
vessels, particularly the small pulmonary alveolar capillaries, leading to endothelial cell activation and
sloughing, coagulopathy, sepsis, pulmonary edema, and ARDS-like symptoms. This is a disease of the
blood and blood vessels. The circulatory system. Any pneumonia that it causes is secondary to that.
In severe cases, this leads to sepsis, blood clots, and multiple organ failure, including hypoxic and
inflammatory damage to various vital organs, such as the brain, heart, liver, pancreas, kidneys, and
intestines.
Some of the most common laboratory findings in COVID-19 are elevated D-dimer, elevated prothrombin
time, elevated C-reactive protein, neutrophilia, lymphopenia, hypocalcemia, and hyperferritinemia,
essentially matching a profile of coagulopathy and immune system hyperactivation/immune cell
exhaustion.
COVID-19 can present as almost anything, due to the wide tropism of SARS-CoV-2 for various tissues in
the body’s vital organs. While its most common initial presentation is respiratory illness and flu-like
symptoms, it can present as brain inflammation, gastrointestinal disease, or even heart attack or
pulmonary embolism.
COVID-19 is more severe in those with specific comorbidities, such as obesity, diabetes, and
hypertension. This is because these conditions involve endothelial dysfunction, which renders the
circulatory system more susceptible to infection and injury by this particular virus.
The vast majority of COVID-19 cases are mild and do not cause significant disease. In known cases, there
is something known as the 80/20 rule, where 80% of cases are mild and 20% are severe or critical.
However, this ratio is only correct for known cases, not all infections. The number of actual infections is
much, much higher. Consequently, the mortality and morbidity rate is lower. However, COVID-19
spreads very quickly, meaning that there are a significant number of severely-ill and critically-ill patients
appearing in a short time frame.
In those who have critical COVID-19-induced sepsis, hypoxia, coagulopathy, and ARDS, the most
common treatments are intubation, injected corticosteroids, and blood thinners. This is not the correct
treatment for COVID-19. In severe hypoxia, cellular metabolic shifts cause ATP to break down into
hypoxanthine, which, upon the reintroduction of oxygen, causes xanthine oxidase to produce tons of
highly damaging radicals that attack tissue. This is called ischemia-reperfusion injury, and it’s why the
majority of people who go on a ventilator are dying. In the mitochondria, succinate buildup due to sepsis
does the same exact thing; when oxygen is reintroduced, it makes superoxide radicals. Make no mistake,
intubation will kill people who have COVID-19.
The end-stage of COVID-19 is severe lipid peroxidation, where fats in the body start to “rust” due to
damage by oxidative stress. This drives autoimmunity. Oxidized lipids appear as foreign objects to the
immune system, which recognizes and forms antibodies against OSEs, or oxidation-specific epitopes.
Also, oxidized lipids feed directly into pattern recognition receptors, triggering even more inflammation
and summoning even more cells of the innate immune system that release even more destructive
enzymes. This is similar to the pathophysiology of Lupus.
COVID-19’s pathology is dominated by extreme oxidative stress and neutrophil respiratory burst, to the
point where hemoglobin becomes incapable of carrying oxygen due to heme iron being stripped out of
heme by hypochlorous acid. No amount of supplemental oxygen can oxygenate blood that chemically
refuses to bind O2.
The breakdown of the pathology is as follows:
SARS-CoV-2 Spike binds to ACE2. Angiotensin Converting Enzyme 2 is an enzyme that is part of the
renin-angiotensin-aldosterone system, or RAAS. The RAAS is a hormone control system that moderates
fluid volume in the body and in the bloodstream (i.e. osmolarity) by controlling salt retention and
excretion. This protein, ACE2, is ubiquitous in every part of the body that interfaces with the circulatory
system, particularly in vascular endothelial cells and pericytes, brain astrocytes, renal tubules and
podocytes, pancreatic islet cells, bile duct and intestinal epithelial cells, and the seminiferous ducts of
the testis, all of which SARS-CoV-2 can infect, not just the lungs.
SARS-CoV-2 infects a cell as follows: SARS-CoV-2 Spike undergoes a conformational change where the S1
trimers flip up and extend, locking onto ACE2 bound to the surface of a cell. TMPRSS2, or
transmembrane protease serine 2, comes along and cuts off the heads of the Spike, exposing the S2
stalk-shaped subunit inside. The remainder of the Spike undergoes a conformational change that causes
it to unfold like an extension ladder, embedding itself in the cell membrane. Then, it folds back upon
itself, pulling the viral membrane and the cell membrane together. The two membranes fuse, with the
virus’s proteins migrating out onto the surface of the cell. The SARS-CoV-2 nucleocapsid enters the cell,
disgorging its genetic material and beginning the viral replication process, hijacking the cell’s own
structures to produce more virus.
SARS-CoV-2 Spike proteins embedded in a cell can actually cause human cells to fuse together, forming
syncytia/MGCs (multinuclear giant cells). They also have other pathogenic, harmful effects. SARS-CoV2’s viroporins, such as its Envelope protein, act as calcium ion channels, introducing calcium into
infected cells. The virus suppresses the natural interferon response, resulting in delayed inflammation.
SARS-CoV-2 N protein can also directly activate the NLRP3 inflammasome. Also, it suppresses the Nrf2
antioxidant pathway. The suppression of ACE2 by binding with Spike causes a buildup of bradykinin that
would otherwise be broken down by ACE2.
This constant calcium influx into the cells results in (or is accompanied by) noticeable hypocalcemia, or
low blood calcium, especially in people with Vitamin D deficiencies and pre-existing endothelial
dysfunction. Bradykinin upregulates cAMP, cGMP, COX, and Phospholipase C activity. This results in
prostaglandin release and vastly increased intracellular calcium signaling, which promotes highly
aggressive ROS release and ATP depletion. NADPH oxidase releases superoxide into the extracellular
space. Superoxide radicals react with nitric oxide to form peroxynitrite. Peroxynitrite reacts with the
tetrahydrobiopterin cofactor needed by endothelial nitric oxide synthase, destroying it and “uncoupling”
the enzymes, causing nitric oxide synthase to synthesize more superoxide instead. This proceeds in a
positive feedback loop until nitric oxide bioavailability in the circulatory system is depleted.
Dissolved nitric oxide gas produced constantly by eNOS serves many important functions, but it is also
antiviral against SARS-like coronaviruses, preventing the palmitoylation of the viral Spike protein and
making it harder for it to bind to host receptors. The loss of NO allows the virus to begin replicating with
impunity in the body. Those with endothelial dysfunction (i.e. hypertension, diabetes, obesity, old age,
African-American race) have redox equilibrium issues to begin with, giving the virus an advantage.
Due to the extreme cytokine release triggered by these processes, the body summons a great deal of
neutrophils and monocyte-derived alveolar macrophages to the lungs. Cells of the innate immune
system are the first-line defenders against pathogens. They work by engulfing invaders and trying to
attack them with enzymes that produce powerful oxidants, like SOD and MPO. Superoxide dismutase
takes superoxide and makes hydrogen peroxide, and myeloperoxidase takes hydrogen peroxide and
chlorine ions and makes hypochlorous acid, which is many, many times more reactive than sodium
hypochlorite bleach.
Neutrophils have a nasty trick. They can also eject these enzymes into the extracellular space, where
they will continuously spit out peroxide and bleach into the bloodstream. This is called neutrophil
extracellular trap formation, or, when it becomes pathogenic and counterproductive, NETosis. In severe
and critical COVID-19, there is actually rather severe NETosis.
Hypochlorous acid building up in the bloodstream begins to bleach the iron out of heme and compete
for O2 binding sites. Red blood cells lose the ability to transport oxygen, causing the sufferer to turn blue
in the face. Unliganded iron, hydrogen peroxide, and superoxide in the bloodstream undergo the HaberWeiss and Fenton reactions, producing extremely reactive hydroxyl radicals that violently strip electrons
from surrounding fats and DNA, oxidizing them severely.
This condition is not unknown to medical science. The actual name for all of this is acute sepsis.
We know this is happening in COVID-19 because people who have died of the disease have noticeable
ferroptosis signatures in their tissues, as well as various other oxidative stress markers such as
nitrotyrosine, 4-HNE, and malondialdehyde.
When you intubate someone with this condition, you are setting off a free radical bomb by supplying
the cells with O2. It’s a catch-22, because we need oxygen to make Adenosine Triphosphate (that is, to
live), but O2 is also the precursor of all these damaging radicals that lead to lipid peroxidation.
The correct treatment for severe COVID-19 related sepsis is non-invasive ventilation, steroids, and
antioxidant infusions. Most of the drugs repurposed for COVID-19 that show any benefit whatsoever in
rescuing critically-ill COVID-19 patients are antioxidants. N-acetylcysteine, melatonin, fluvoxamine,
budesonide, famotidine, cimetidine, and ranitidine are all antioxidants. Indomethacin prevents irondriven oxidation of arachidonic acid to isoprostanes. There are powerful antioxidants such as apocynin
that have not even been tested on COVID-19 patients yet which could defang neutrophils, prevent lipid
peroxidation, restore endothelial health, and restore oxygenation to the tissues.
Scientists who know anything about pulmonary neutrophilia, ARDS, and redox biology have known or
surmised much of this since March 2020. In April 2020, Swiss scientists confirmed that COVID-19 was a
vascular endotheliitis. By late 2020, experts had already concluded that COVID-19 causes a form of viral
sepsis. They also know that sepsis can be effectively treated with antioxidants. None of this information
is particularly new, and yet, for the most part, it has not been acted upon. Doctors continue to use
damaging intubation techniques with high PEEP settings despite high lung compliance and poor
oxygenation, killing an untold number of critically ill patients with medical malpractice.
Because of the way they are constructed, Randomized Control Trials will never show any benefit for any
antiviral against COVID-19. Not Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The reason for this
is simple; for the patients that they have recruited for these studies, such as Oxford’s ludicrous
RECOVERY study, the intervention is too late to have any positive effect.
The clinical course of COVID-19 is such that by the time most people seek medical attention for hypoxia,
their viral load has already tapered off to almost nothing. If someone is about 10 days post-exposure
and has already been symptomatic for five days, there is hardly any virus left in their bodies, only
cellular damage and derangement that has initiated a hyperinflammatory response. It is from this group
that the clinical trials for antivirals have recruited, pretty much exclusively.
In these trials, they give antivirals to severely ill patients who have no virus in their bodies, only a
delayed hyperinflammatory response, and then absurdly claim that antivirals have no utility in treating
or preventing COVID-19. These clinical trials do not recruit people who are pre-symptomatic. They do
not test pre-exposure or post-exposure prophylaxis.
This is like using a defibrillator to shock only flatline, and then absurdly claiming that defibrillators have
no medical utility whatsoever when the patients refuse to rise from the dead. The intervention is too
late. These trials for antivirals show systematic, egregious selection bias. They are providing a treatment
that is futile to the specific cohort they are enrolling.
India went against the instructions of the WHO and mandated the prophylactic usage of Ivermectin.
They have almost completely eradicated COVID-19. The Indian Bar Association of Mumbai has brought
criminal charges against WHO Chief Scientist Dr. Soumya Swaminathan for recommending against the
use of Ivermectin.
Ivermectin is not “horse dewormer”. Yes, it is sold in veterinary paste form as a dewormer for animals. It
has also been available in pill form for humans for decades, as an antiparasitic drug.
The media have disingenuously claimed that because Ivermectin is an antiparasitic drug, it has no utility
as an antivirus. This is incorrect. Ivermectin has utility as an antiviral. It blocks importin, preventing
nuclear import, effectively inhibiting viral access to cell nuclei. Many drugs currently on the market have
multiple modes of action. Ivermectin is one such drug. It is both antiparasitic and antiviral.
In Bangladesh, Ivermectin costs $1.80 for an entire 5-day course. Remdesivir, which is toxic to the liver,
costs $3,120 for a 5-day course of the drug. Billions of dollars of utterly useless Remdesivir were sold to
our governments on the taxpayer’s dime, and it ended up being totally useless for treating
hyperinflammatory COVID-19. The media has hardly even covered this at all.
The opposition to the use of generic Ivermectin is not based in science. It is purely financially and
politically-motivated. An effective non-vaccine intervention would jeopardize the rushed FDA approval
of patented vaccines and medicines for which the pharmaceutical industry stands to rake in billions
upon billions of dollars in sales on an ongoing basis.
The majority of the public are scientifically illiterate and cannot grasp what any of this even means,
thanks to a pathetic educational system that has miseducated them. You would be lucky to find 1 in 100
people who have even the faintest clue what any of this actually means.
COVID-19 Transmission:
COVID-19 is airborne. The WHO carried water for China by claiming that the virus was only dropletborne. Our own CDC absurdly claimed that it was mostly transmitted by fomite-to-face contact, which,
given its rapid spread from Wuhan to the rest of the world, would have been physically impossible.
The ridiculous belief in fomite-to-face being a primary mode of transmission led to the use of surface
disinfection protocols that wasted time, energy, productivity, and disinfectant.
The 6-foot guidelines are absolutely useless. The minimum safe distance to protect oneself from an
aerosolized virus is to be 15+ feet away from an infected person, no closer. Realistically, no public transit
is safe.
Surgical masks do not protect you from aerosols. The virus is too small and the filter media has too large
of gaps to filter it out. They may catch respiratory droplets and keep the virus from being expelled by
someone who is sick, but they do not filter a cloud of infectious aerosols if someone were to walk into
said cloud.
The minimum level of protection against this virus is quite literally a P100 respirator, a PAPR/CAPR, or a
40mm NATO CBRN respirator, ideally paired with a full-body tyvek or tychem suit, gloves, and booties,
with all the holes and gaps taped.
Live SARS-CoV-2 may potentially be detected in sewage outflows, and there may be oral-fecal
transmission. During the SARS outbreak in 2003, in the Amoy Gardens incident, hundreds of people
were infected by aerosolized fecal matter rising from floor drains in their apartments.
COVID-19 Vaccine Dangers:
The vaccines for COVID-19 are not sterilizing and do not prevent infection or transmission. They are
“leaky” vaccines. This means they remove the evolutionary pressure on the virus to become less lethal.
It also means that the vaccinated are perfect carriers. In other words, those who are vaccinated are a
threat to the unvaccinated, not the other way around.
All of the COVID-19 vaccines currently in use have undergone minimal testing, with highly accelerated
clinical trials. Though they appear to limit severe illness, the long-term safety profile of these vaccines
remains unknown.
Some of these so-called “vaccines” utilize an untested new technology that has never been used in
vaccines before. Traditional vaccines use weakened or killed virus to stimulate an immune response. The
Moderna and Pfizer-BioNTech vaccines do not. They are purported to consist of an intramuscular shot
containing a suspension of lipid nanoparticles filled with messenger RNA. The way they generate an
immune response is by fusing with cells in a vaccine recipient’s shoulder, undergoing endocytosis,
releasing their mRNA cargo into those cells, and then utilizing the ribosomes in those cells to synthesize
modified SARS-CoV-2 Spike proteins in-situ.
These modified Spike proteins then migrate to the surface of the cell, where they are anchored in place
by a transmembrane domain. The adaptive immune system detects the non-human viral protein being
expressed by these cells, and then forms antibodies against that protein. This is purported to confer
protection against the virus, by training the adaptive immune system to recognize and produce
antibodies against the Spike on the actual virus. The J&J and AstraZeneca vaccines do something similar,
but use an adenovirus vector for genetic material delivery instead of a lipid nanoparticle. These vaccines
were produced or validated with the aid of fetal cell lines HEK-293 and PER.C6, which people with
certain religious convictions may object strongly to.
SARS-CoV-2 Spike is a highly pathogenic protein on its own. It is impossible to overstate the danger
presented by introducing this protein into the human body.
It is claimed by vaccine manufacturers that the vaccine remains in cells in the shoulder, and that SARSCoV-2 Spike produced and expressed by these cells from the vaccine’s genetic material is harmless and
inert, thanks to the insertion of prolines in the Spike sequence to stabilize it in the prefusion
conformation, preventing the Spike from becoming active and fusing with other cells. However, a
pharmacokinetic study from Japan showed that the lipid nanoparticles and mRNA from the Pfizer
vaccine did not stay in the shoulder, and in fact bioaccumulated in many different organs, including the
reproductive organs and adrenal glands, meaning that modified Spike is being expressed quite literally
all over the place. These lipid nanoparticles may trigger anaphylaxis in an unlucky few, but far more
concerning is the unregulated expression of Spike in various somatic cell lines far from the injection site
and the unknown consequences of that.
Messenger RNA is normally consumed right after it is produced in the body, being translated into a
protein by a ribosome. COVID-19 vaccine mRNA is produced outside the body, long before a ribosome
translates it. In the meantime, it could accumulate damage if inadequately preserved. When a ribosome
attempts to translate a damaged strand of mRNA, it can become stalled. When this happens, the
ribosome becomes useless for translating proteins because it now has a piece of mRNA stuck in it, like a
lace card in an old punch card reader. The whole thing has to be cleaned up and new ribosomes
synthesized to replace it. In cells with low ribosome turnover, like nerve cells, this can lead to reduced
protein synthesis, cytopathic effects, and neuropathies.
Certain proteins, including SARS-CoV-2 Spike, have proteolytic cleavage sites that are basically like little
dotted lines that say “cut here”, which attract a living organism’s own proteases (essentially, molecular
scissors) to cut them. There is a possibility that S1 may be proteolytically cleaved from S2, causing active
S1 to float away into the bloodstream while leaving the S2 “stalk” embedded in the membrane of the
cell that expressed the protein.
SARS-CoV-2 Spike has a Superantigenic region (SAg), which may promote extreme inflammation.
Anti-Spike antibodies were found in one study to function as autoantibodies and attack the body’s own
cells. Those who have been immunized with COVID-19 vaccines have developed blood clots,
myocarditis, Guillain-Barre Syndrome, Bell’s Palsy, and multiple sclerosis flares, indicating that the
vaccine promotes autoimmune reactions against healthy tissue.
SARS-CoV-2 Spike does not only bind to ACE2. It was suspected to have regions that bind to basigin,
integrins, neuropilin-1, and bacterial lipopolysaccharides as well. SARS-CoV-2 Spike, on its own, can
potentially bind any of these things and act as a ligand for them, triggering unspecified and likely highly
inflammatory cellular activity.
SARS-CoV-2 Spike contains an unusual PRRA insert that forms a furin cleavage site. Furin is a ubiquitous
human protease, making this an ideal property for the Spike to have, giving it a high degree of cell
tropism. No wild-type SARS-like coronaviruses related to SARS-CoV-2 possess this feature, making it
highly suspicious, and perhaps a sign of human tampering.
SARS-CoV-2 Spike has a prion-like domain that enhances its infectiousness.
The Spike S1 RBD may bind to heparin-binding proteins and promote amyloid aggregation. In humans,
this could lead to Parkinson’s, Lewy Body Dementia, premature Alzheimer’s, or various other
neurodegenerative diseases. This is very concerning because SARS-CoV-2 S1 is capable of injuring and
penetrating the blood-brain barrier and entering the brain. It is also capable of increasing the
permeability of the blood-brain barrier to other molecules.
SARS-CoV-2, like other betacoronaviruses, may have Dengue-like ADE, or antibody-dependent
enhancement of disease. For those who aren’t aware, some viruses, including betacoronaviruses, have a
feature called ADE. There is also something called Original Antigenic Sin, which is the observation that
the body prefers to produce antibodies based on previously-encountered strains of a virus over newlyencountered ones.
In ADE, antibodies from a previous infection become non-neutralizing due to mutations in the virus’s
proteins. These non-neutralizing antibodies then act as trojan horses, allowing live, active virus to be
pulled into macrophages through their Fc receptor pathways, allowing the virus to infect immune cells
that it would not have been able to infect before. This has been known to happen with Dengue Fever;
when someone gets sick with Dengue, recovers, and then contracts a different strain, they can get very,
very ill.
If someone is vaccinated with mRNA based on the Spike from the initial Wuhan strain of SARS-CoV-2,
and then they become infected with a future, mutated strain of the virus, they may become severely ill.
In other words, it is possible for vaccines to sensitize someone to disease.
There is a precedent for this in recent history. Sanofi’s Dengvaxia vaccine for Dengue failed because it
caused immune sensitization in people whose immune systems were Dengue-naïve.
In mice immunized against SARS-CoV and challenged with the virus, a close relative of SARS-CoV-2, they
developed immune sensitization, Th2 immunopathology, and eosinophil infiltration in their lungs.
We have been told that SARS-CoV-2 mRNA vaccines cannot be integrated into the human genome,
because messenger RNA cannot be turned back into DNA. This is false. There are elements in human
cells called LINE-1 retrotransposons, which can indeed integrate mRNA into a human genome by
endogenous reverse transcription. Because the mRNA used in the vaccines is stabilized, it hangs around
in cells longer, increasing the chances for this to happen. If the gene for SARS-CoV-2 Spike is integrated
into a portion of the genome that is not silent and actually expresses a protein, it is possible that people
who take this vaccine may continuously express SARS-CoV-2 Spike from their somatic cells for the rest of
their lives.
By inoculating people with a vaccine that causes their bodies to produce Spike in-situ, they are being
inoculated with a pathogenic protein. A toxin that may cause long-term inflammation, heart problems,
and a raised risk of cancers. In the long-term, it may also potentially lead to premature
neurodegenerative disease.
Absolutely nobody should be compelled to take this vaccine under any circumstances, and in actual fact,
the vaccination campaign must be stopped immediately.
COVID-19 Criminal Conspiracy:
The vaccine and the virus were made by the same people.
In 2014, there was a moratorium on SARS gain-of-function research that lasted until 2017. This research
was not halted. Instead, it was outsourced, with the federal grants being laundered through NGOs.
Ralph Baric is a virologist and SARS expert at UNC Chapel Hill in North Carolina. This is who Anthony
Fauci was referring to when he insisted, before Congress, that if any gain-of-function research was being
conducted, it was being conducted in North Carolina.
This was a lie. Anthony Fauci lied before Congress. A felony.
Ralph Baric and Shi Zhengli are colleagues and have co-written papers together. Ralph Baric mentored
Shi Zhengli in his gain-of-function manipulation techniques, particularly serial passage, which results in a
virus that appears as if it originated naturally. In other words, deniable bioweapons. Serial passage in
humanized hACE2 mice may have produced something like SARS-CoV-2.
The funding for the gain-of-function research being conducted at the Wuhan Institute of Virology came
from Peter Daszak. Peter Daszak runs an NGO called EcoHealth Alliance. EcoHealth Alliance received
millions of dollars in grant money from the National Institutes of Health/National Institute of Allergy and
Infectious Diseases (that is, Anthony Fauci), the Defense Threat Reduction Agency (part of the US
Department of Defense), and the United States Agency for International Development. NIH/NIAID
contributed a few million dollars, and DTRA and USAID each contributed tens of millions of dollars
towards this research. Altogether, it was over a hundred million dollars.
EcoHealth Alliance subcontracted these grants to the Wuhan Institute of Virology, a lab in China with a
very questionable safety record and poorly trained staff, so that they could conduct gain-of-function
research, not in their fancy P4 lab, but in a level-2 lab where technicians wore nothing more
sophisticated than perhaps a hairnet, latex gloves, and a surgical mask, instead of the bubble suits used
when working with dangerous viruses. Chinese scientists in Wuhan reported being routinely bitten and
urinated on by laboratory animals. Why anyone would outsource this dangerous and delicate work to
the People’s Republic of China, a country infamous for industrial accidents and massive explosions that
have claimed hundreds of lives, is completely beyond me, unless the aim was to start a pandemic on
purpose.
In November of 2019, three technicians at the Wuhan Institute of Virology developed symptoms
consistent with a flu-like illness. Anthony Fauci, Peter Daszak, and Ralph Baric knew at once what had
happened, because back channels exist between this laboratory and our scientists and officials.
December 12th, 2019, Ralph Baric signed a Material Transfer Agreement (essentially, an NDA) to receive
Coronavirus mRNA vaccine-related materials co-owned by Moderna and NIH. It wasn’t until a whole
month later, on January 11th, 2020, that China allegedly sent us the sequence to what would become
known as SARS-CoV-2. Moderna claims, rather absurdly, that they developed a working vaccine from
this sequence in under 48 hours.
Stéphane Bancel, the current CEO of Moderna, was formerly the CEO of bioMérieux, a French
multinational corporation specializing in medical diagnostic tech, founded by one Alain Mérieux. Alain
Mérieux was one of the individuals who was instrumental in the construction of the Wuhan Institute of
Virology’s P4 lab.
The sequence given as the closest relative to SARS-CoV-2, RaTG13, is not a real virus. It is a forgery. It
was made by entering a gene sequence by hand into a database, to create a cover story for the
existence of SARS-CoV-2, which is very likely a gain-of-function chimera produced at the Wuhan Institute
of Virology and was either leaked by accident or intentionally released.
The animal reservoir of SARS-CoV-2 has never been found.
This is not a conspiracy “theory”. It is an actual criminal conspiracy, in which people connected to the
development of Moderna’s mRNA-1273 are directly connected to the Wuhan Institute of Virology and
their gain-of-function research by very few degrees of separation, if any. The paper trail is wellestablished.
The lab-leak theory has been suppressed because pulling that thread leads one to inevitably conclude
that there is enough circumstantial evidence to link Moderna, the NIH, the WIV, and both the vaccine
and the virus’s creation together. In a sane country, this would have immediately led to the world’s
biggest RICO and mass murder case. Anthony Fauci, Peter Daszak, Ralph Baric, Shi Zhengli, and Stéphane
Bancel, and their accomplices, would have been indicted and prosecuted to the fullest extent of the law.
Instead, billions of our tax dollars were awarded to the perpetrators.
The FBI raided Allure Medical in Shelby Township north of Detroit for billing insurance for “fraudulent
COVID-19 cures”. The treatment they were using? Intravenous Vitamin C. An antioxidant. Which, as
described above, is an entirely valid treatment for COVID-19-induced sepsis, and indeed, is now part of
the MATH+ protocol advanced by Dr. Paul E. Marik.
The FDA banned ranitidine (Zantac) due to supposed NDMA (N-nitrosodimethylamine) contamination.
Ranitidine is not only an H2 blocker used as antacid, but also has a powerful antioxidant effect,
scavenging hydroxyl radicals. This gives it utility in treating COVID-19.
The FDA also attempted to take N-acetylcysteine, a harmless amino acid supplement and antioxidant,
off the shelves, compelling Amazon to remove it from their online storefront.
This leaves us with a chilling question: did the FDA knowingly suppress antioxidants useful for treating
COVID-19 sepsis as part of a criminal conspiracy against the American public?
The establishment is cooperating with, and facilitating, the worst criminals in human history, and are
actively suppressing non-vaccine treatments and therapies in order to compel us to inject these
criminals’ products into our bodies. This is absolutely unacceptable.
COVID-19 Vaccine Development and Links to Transhumanism:
This section deals with some more speculative aspects of the pandemic and the medical and scientific
establishment’s reaction to it, as well as the disturbing links between scientists involved in vaccine
research and scientists whose work involved merging nanotechnology with living cells.
On June 9th, 2020, Charles Lieber, a Harvard nanotechnology researcher with decades of experience, was
indicted by the DOJ for fraud. Charles Lieber received millions of dollars in grant money from the US
Department of Defense, specifically the military think tanks DARPA, AFOSR, and ONR, as well as NIH and
MITRE. His specialty is the use of silicon nanowires in lieu of patch clamp electrodes to monitor and
modulate intracellular activity, something he has been working on at Harvard for the past twenty years.
He was claimed to have been working on silicon nanowire batteries in China, but none of his colleagues
can recall him ever having worked on battery technology in his life; all of his research deals with
bionanotechnology, or the blending of nanotech with living cells.
The indictment was over his collaboration with the Wuhan University of Technology. He had doubledipped, against the terms of his DOD grants, and taken money from the PRC’s Thousand Talents plan, a
program which the Chinese government uses to bribe Western scientists into sharing proprietary R&D
information that can be exploited by the PLA for strategic advantage.
Charles Lieber’s own papers describe the use of silicon nanowires for brain-computer interfaces, or
“neural lace” technology. His papers describe how neurons can endocytose whole silicon nanowires or
parts of them, monitoring and even modulating neuronal activity.
Charles Lieber was a colleague of Robert Langer. Together, along with Daniel S. Kohane, they worked on
a paper describing artificial tissue scaffolds that could be implanted in a human heart to monitor its
activity remotely.
Robert Langer, an MIT alumnus and expert in nanotech drug delivery, is one of the co-founders of
Moderna. His net worth is now $5.1 billion USD thanks to Moderna’s mRNA-1273 vaccine sales.
Both Charles Lieber and Robert Langer’s bibliographies describe, essentially, techniques for human
enhancement, i.e. transhumanism. Klaus Schwab, the founder of the World Economic Forum and the
architect behind the so-called “Great Reset”, has long spoken of the “blending of biology and
machinery” in his books.
Since these revelations, it has come to the attention of independent researchers that the COVID-19
vaccines may contain reduced graphene oxide nanoparticles. Japanese researchers have also found
unexplained contaminants in COVID-19 vaccines.
Graphene oxide is an anxiolytic. It has been shown to reduce the anxiety of laboratory mice when
injected into their brains. Indeed, given SARS-CoV-2 Spike’s propensity to compromise the blood-brain
barrier and increase its permeability, it is the perfect protein for preparing brain tissue for extravasation
of nanoparticles from the bloodstream and into the brain. Graphene is also highly conductive and, in
some circumstances, paramagnetic.
In 2013, under the Obama administration, DARPA launched the BRAIN Initiative; BRAIN is an acronym
for Brain Research Through Advancing Innovative Neurotechnologies®. This program involves the
development of brain-computer interface technologies for the military, particularly non-invasive,
injectable systems that cause minimal damage to brain tissue when removed. Supposedly, this
technology would be used for healing wounded soldiers with traumatic brain injuries, the direct brain
control of prosthetic limbs, and even new abilities such as controlling drones with one’s mind.
Various methods have been proposed for achieving this, including optogenetics, magnetogenetics,
ultrasound, implanted electrodes, and transcranial electromagnetic stimulation. In all instances, the goal
is to obtain read or read-write capability over neurons, either by stimulating and probing them, or by
rendering them especially sensitive to stimulation and probing.
However, the notion of the widespread use of BCI technology, such as Elon Musk’s Neuralink device,
raises many concerns over privacy and personal autonomy. Reading from neurons is problematic
enough on its own. Wireless brain-computer interfaces may interact with current or future wireless GSM
infrastructure, creating neurological data security concerns. A hacker or other malicious actor may
compromise such networks to obtain people’s brain data, and then exploit it for nefarious purposes.
However, a device capable of writing to human neurons, not just reading from them, presents another,
even more serious set of ethical concerns. A BCI that is capable of altering the contents of one’s mind
for innocuous purposes, such as projecting a heads-up display onto their brain’s visual center or sending
audio into one’s auditory cortex, would also theoretically be capable of altering mood and personality,
or perhaps even subjugating someone’s very will, rendering them utterly obedient to authority. This
technology would be a tyrant’s wet dream. Imagine soldiers who would shoot their own countrymen
without hesitation, or helpless serfs who are satisfied to live in literal dog kennels.
BCIs could be used to unscrupulously alter perceptions of basic things such as emotions and values,
changing people’s thresholds of satiety, happiness, anger, disgust, and so forth. This is not
inconsequential. Someone’s entire regime of behaviors could be altered by a BCI, including such things
as suppressing their appetite or desire for virtually anything on Maslow’s Hierarchy of Needs.
Anything is possible when you have direct access to someone’s brain and its contents. Someone who is
obese could be made to feel disgust at the sight of food. Someone who is involuntarily celibate could
have their libido disabled so they don’t even desire sex to begin with. Someone who is racist could be
forced to feel delight over cohabiting with people of other races. Someone who is violent could be
forced to be meek and submissive. These things might sound good to you if you are a tyrant, but to
normal people, the idea of personal autonomy being overridden to such a degree is appalling.
For the wealthy, neural laces would be an unequaled boon, giving them the opportunity to enhance
their intelligence with neuroprosthetics (i.e. an “exocortex”), and to deliver irresistible commands
directly into the minds of their BCI-augmented servants, even physically or sexually abusive commands
that they would normally refuse.
If the vaccine is a method to surreptitiously introduce an injectable BCI into millions of people without
their knowledge or consent, then what we are witnessing is the rise of a tyrannical regime unlike
anything ever seen before on the face of this planet, one that fully intends to strip every man, woman,
and child of our free will.
Our flaws are what make us human. A utopia arrived at by removing people’s free will is not a utopia at
all. It is a monomaniacal nightmare. Furthermore, the people who rule over us are Dark Triad types who
cannot be trusted with such power. Imagine being beaten and sexually assaulted by a wealthy and
powerful psychopath and being forced to smile and laugh over it because your neural lace gives you no
choice but to obey your master.
The Elites are forging ahead with this technology without giving people any room to question the social
or ethical ramifications, or to establish regulatory frameworks that ensure that our personal agency and
autonomy will not be overridden by these devices. They do this because they secretly dream of a future
where they can treat you worse than an animal and you cannot even fight back. If this evil plan is
allowed to continue, it will spell the end of humanity as we know it.
Conclusions:
The current pandemic was produced and perpetuated by the establishment, through the use of a virus
engineered in a PLA-connected Chinese biowarfare laboratory, with the aid of American taxpayer dollars
and French expertise.
This research was conducted under the absolutely ridiculous euphemism of “gain-of-function” research,
which is supposedly carried out in order to determine which viruses have the highest potential for
zoonotic spillover and preemptively vaccinate or guard against them.
Gain-of-function/gain-of-threat research, a.k.a. “Dual-Use Research of Concern”, or DURC, is bioweapon
research by another, friendlier-sounding name, simply to avoid the taboo of calling it what it actually is.
It has always been bioweapon research. The people who are conducting this research fully understand
that they are taking wild pathogens that are not infectious in humans and making them more infectious,
often taking grants from military think tanks encouraging them to do so.
These virologists conducting this type of research are enemies of their fellow man, like pyromaniac
firefighters. GOF research has never protected anyone from any pandemic. In fact, it has now started
one, meaning its utility for preventing pandemics is actually negative. It should have been banned
globally, and the lunatics performing it should have been put in straitjackets long ago.
Either through a leak or an intentional release from the Wuhan Institute of Virology, a deadly SARS
strain is now endemic across the globe, after the WHO and CDC and public officials first downplayed the
risks, and then intentionally incited a panic and lockdowns that jeopardized people’s health and their
livelihoods.
This was then used by the utterly depraved and psychopathic aristocratic class who rule over us as an
excuse to coerce people into accepting an injected poison which may be a depopulation agent, a mind
control/pacification agent in the form of injectable “smart dust”, or both in one. They believe they can
get away with this by weaponizing the social stigma of vaccine refusal. They are incorrect.
Their motives are clear and obvious to anyone who has been paying attention. These megalomaniacs
have raided the pension funds of the free world. Wall Street is insolvent and has had an ongoing
liquidity crisis since the end of 2019. The aim now is to exert total, full-spectrum physical, mental, and
financial control over humanity before we realize just how badly we’ve been extorted by these maniacs.
The pandemic and its response served multiple purposes for the Elite:
• Concealing a depression brought on by the usurious plunder of our economies conducted by
rentier-capitalists and absentee owners who produce absolutely nothing of any value to society
whatsoever. Instead of us having a very predictable Occupy Wall Street Part II, the Elites and
their stooges got to stand up on television and paint themselves as wise and all-powerful saviors
instead of the marauding cabal of despicable land pirates that they are.
• Destroying small businesses and eroding the middle class.
• Transferring trillions of dollars of wealth from the American public and into the pockets of
billionaires and special interests.
• Engaging in insider trading, buying stock in biotech companies and shorting brick-and-mortar
businesses and travel companies, with the aim of collapsing face-to-face commerce and tourism
and replacing it with e-commerce and servitization.
• Creating a casus belli for war with China, encouraging us to attack them, wasting American lives
and treasure and driving us to the brink of nuclear armageddon.
• Establishing technological and biosecurity frameworks for population control and technocraticsocialist “smart cities” where everyone’s movements are despotically tracked, all in anticipation
of widespread automation, joblessness, and food shortages, by using the false guise of a vaccine
to compel cooperation.
Any one of these things would constitute a vicious rape of Western society. Taken together, they beggar
belief; they are a complete inversion of our most treasured values.
What is the purpose of all of this? One can only speculate as to the perpetrators’ motives, however, we
have some theories.
The Elites are trying to pull up the ladder, erase upward mobility for large segments of the population,
cull political opponents and other “undesirables”, and put the remainder of humanity on a tight leash,
rationing our access to certain goods and services that they have deemed “high-impact”, such as
automobile use, tourism, meat consumption, and so on. Naturally, they will continue to have their own
luxuries, as part of a strict caste system akin to feudalism.
Why are they doing this? Simple. The Elites are Neo-Malthusians and believe that we are overpopulated
and that resource depletion will collapse civilization in a matter of a few short decades. They are not
necessarily incorrect in this belief. We are overpopulated, and we are consuming too many resources.
However, orchestrating such a gruesome and murderous power grab in response to a looming crisis
demonstrates that they have nothing but the utmost contempt for their fellow man.
To those who are participating in this disgusting farce without any understanding of what they are
doing, we have one word for you. Stop. You are causing irreparable harm to your country and to your
fellow citizens.
To those who may be reading this warning and have full knowledge and understanding of what they are
doing and how it will unjustly harm millions of innocent people, we have a few more words.
Damn you to hell. You will not destroy America and the Free World, and you will not have your New
World Order. We will make certain of that.

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://www.dovepress.com/obesity-related-inflammation-and-endothelial-dysfunction-in-covid-19-ipeer-reviewed-fulltext-article-JIR
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 reninangiotensin-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):
https://scitechdaily.com/nitric-oxide-a-possible-treatment-for-covid-19-only-substance-to-have-adirect-effect-on-sars-cov-2/
Those with endothelial dysfunction (i.e. hypertension, diabetes, obesity, old age, African-American race)
have redox equilibrium issues to begin with, giving the virus an advantage:
https://www.nature.com/articles/s41392-020-00454-7
https://www.frontiersin.org/articles/10.3389/fphys.2020.605908/full
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430889/
https://pubmed.ncbi.nlm.nih.gov/19004510/
Due to the extreme cytokine release triggered by these processes, the body summons a great deal of
neutrophils and monocyte-derived alveolar macrophages to the lungs:
https://www.frontiersin.org/articles/10.3389/fimmu.2021.652470/full
https://www.frontiersin.org/articles/10.3389/fimmu.2021.720109/full
Phagocytic cells of the innate immune system are the first-line defenders against pathogens. They work
by engulfing invaders and trying to attack them with enzymes that produce powerful oxidants, like SOD
and MPO:
https://www.frontiersin.org/articles/10.3389/fimmu.2012.00174/full
https://jlb.onlinelibrary.wiley.com/doi/full/10.1189/jlb.0809549
Superoxide dismutase takes superoxide and makes hydrogen peroxide, and myeloperoxidase takes
hydrogen peroxide and chlorine ions and makes hypochlorous acid, which is many, many times more
reactive than sodium hypochlorite bleach:
https://www.sciencedirect.com/topics/neuroscience/superoxide-dismutase
https://www.sciencedirect.com/topics/medicine-and-dentistry/myeloperoxidase
In severe and critical COVID-19, there is actually rather severe NETosis:
https://www.frontiersin.org/articles/10.3389/fphar.2021.708302/full
https://insight.jci.org/articles/view/138999
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184981/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488868/
https://ashpublications.org/blood/article/136/10/1169/461219/Neutrophil-extracellular-trapscontribute-to
https://www.sciencedirect.com/science/article/pii/S221249262030052X
Hypochlorous acid building up in the bloodstream begins to bleach the iron out of heme and compete for
O2 binding sites. Red blood cells lose the ability to transport oxygen, causing the sufferer to turn blue in
the face:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757048/
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0120737
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863623/
Unliganded iron, hydrogen peroxide, and superoxide in the bloodstream undergo the Haber-Weiss and
Fenton reactions, producing extremely reactive hydroxyl radicals that violently strip electrons from
surrounding fats and DNA, oxidizing them severely:
https://www.sciencedirect.com/science/article/pii/S0753332221000135
https://sites.kowsarpub.com/ans/articles/60038.html
https://www.sciencedirect.com/science/article/abs/pii/S0300483X00002316?via%3Dihub
https://www.sciencedirect.com/topics/chemistry/fenton-reaction
https://www.researchgate.net/figure/Fenton-and-Haber-Weiss-reactions-are-a-source-of-oxidativestress-The-generation-of_fig1_330729897
This condition is not unknown to medical science. The actual name for all of this is acute sepsis (but
without the traditional hallmarks of sepsis, like shock):
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056356/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886971/
https://www.futuremedicine.com/doi/10.2217/fmb-2020-0312
https://www.global-sepsis-alliance.org/news/2020/4/7/update-can-covid-19-cause-sepsis-explainingthe-relationship-between-the-coronavirus-disease-and-sepsis-cvd-novel-coronavirus
We know this is happening in COVID-19 because people who have died of the disease have noticeable
ferroptosis signatures in their tissues, as well as various other oxidative stress markers such as
nitrotyrosine, 4-HNE, and malondialdehyde:
https://onlinelibrary.wiley.com/doi/full/10.1002/ehf2.12958
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264936/
https://www.sciencedirect.com/science/article/pii/S2213231721001300
https://www.researchgate.net/publication/354129433_Preliminary_Findings_on_the_Association_of_t
he_Lipid_Peroxidation_Product_4-Hydroxynonenal_with_the_Lethal_Outcome_of_Aggressive_COVID19
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180845/
https://rupress.org/jem/article-abstract/218/6/e20210518/212093/Ferroptosis-in-infectioninflammation-and?redirectedFrom=fulltext
When you intubate someone with this condition, you are setting off a free radical bomb by supplying the
cells with O2. It’s a catch-22, because we need oxygen to make Adenosine Triphosphate (that is, to live),
but O2 is also the precursor of all these damaging radicals that lead to lipid peroxidation:
https://www.nature.com/articles/pr2009174
The correct treatment for severe COVID-19 related sepsis is non-invasive ventilation, steroids, and
antioxidant infusions:
https://covid19criticalcare.com/covid-19-protocols/math-plus-protocol/
https://journals.lww.com/ccmjournal/Abstract/2007/09001/Antioxidant_supplementation_in_sepsis_a
nd_systemic.25.aspx
https://mdpi-res.com/d_attachment/medicina/medicina-56-00619/article_deploy/medicina-56-00619-
v2.pdf
Most of the drugs repurposed for COVID-19 that show any benefit whatsoever in rescuing critically-ill
COVID-19 patients are antioxidants. N-acetylcysteine, melatonin, fluvoxamine, budesonide, famotidine,
cimetidine, and ranitidine are all antioxidants:
https://www.hindawi.com/journals/omcl/2018/6581970/
https://www.intechopen.com/chapters/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
They also know that sepsis can be effectively treated with antioxidants:
https://jtd.amegroups.com/article/view/34870/html
https://www.evms.edu/about_evms/administrative_offices/marketing_communications/publications/is
sue_9_4/has-sepsis-met-its-match.php
None of this information is particularly new, and yet, for the most part, it has not been acted upon.
Doctors continue to use damaging intubation techniques with high PEEP settings despite high lung
compliance and poor oxygenation, killing an untold number of critically ill patients with medical
malpractice:
https://ccforum.biomedcentral.com/articles/10.1186/s13054-020-03049-4
https://jamanetwork.com/journals/jama/fullarticle/2765302
Because of the way they are constructed, Randomized Control Trials will never show any benefit for any
antiviral against COVID-19. Not Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The reason for this
is simple; for the patients that they have enrolled in these studies, such as Oxford’s ludicrous RECOVERY
study, the intervention is too late to have any positive effect (i.e. these RCTs are designed in such a way
that the use of antivirals is futile, therefore, these studies are deceptive and unethical by their very
nature):
https://www.mdpi.com/1999-4915/13/6/963/htm
The clinical course of COVID-19 is such that by the time most people seek medical attention for hypoxia,
their viral load has already tapered off to almost nothing. If someone is about 10 days post-exposure and
has already been symptomatic for five days, there is hardly any virus left in their bodies, only cellular
damage and derangement that has initiated a hyperinflammatory response:
https://www.the-hospitalist.org/hospitalist/article/234869/coronavirus-updates/state-inpatient-covid19-care
https://www.sciencedirect.com/science/article/pii/S0753332220306867
It is from this group that the clinical trials for antivirals have recruited, pretty much exclusively (i.e. they
do not test prophylaxis/early treatment, only changes to the mean duration of hospitalization for those
already hospitalized):
https://www.nejm.org/doi/full/10.1056/nejmoa2023184
https://www.nejm.org/doi/full/10.1056/NEJMoa2022926
https://pubmed.ncbi.nlm.nih.gov/34318930/
India went against the instructions of the WHO and mandated the prophylactic usage of Ivermectin. They
have almost completely eradicated COVID-19:
https://wentworthreport.com/2021/09/11/ivermectin-wins-in-india/
https://ivmmeta.com
The Indian Bar Association of Mumbai has brought criminal charges against WHO Chief Scientist Dr.
Soumya Swaminathan for recommending against the use of Ivermectin:
https://indianbarassociation.in/wp-content/uploads/2021/05/IBA-PRESS-RELEASE-MAY-26-2021.pdf
Ivermectin is not “horse dewormer”. Yes, it is sold in veterinary paste form as a dewormer for animals. It
has also been available in pill form for humans for decades, as an antiparasitic drug:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043740/
The media have disingenuously claimed that because Ivermectin is an antiparasitic drug, it has no utility
as an antivirus. This is incorrect. Ivermectin has utility as an antiviral. It blocks importin, 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:
https://journals.lww.com/americantherapeutics/fulltext/2021/08000/ivermectin_for_prevention_and_t
reatment_of.7.aspx
Remdesivir, which is toxic to the liver, costs $3,120 for a 5-day course of the drug:
https://www.npr.org/sections/health-shots/2020/06/29/884648842/remdesivir-priced-at-more-than-3-
100-for-a-course-of-treatment
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.fiercepharma.com/pharma/gilead-s-1-5b-remdesivir-sales-help-buoy-greater-thanexpected-declines-for-mainstay-hiv
https://www.forbes.com/sites/jvchamary/2021/01/31/remdesivir-covidcoronavirus/?sh=7e6034e666c2
COVID-19 is airborne. The WHO carried water for China by claiming that the virus was only dropletborne. Our own CDC absurdly claimed that it was mostly transmitted by fomite-to-face contact, which,
given its rapid spread from Wuhan to the rest of the world, would have been physically impossible:
https://www.thelancet.com/article/S0140-6736(21)00869-2/fulltext
https://www.pennmedicine.org/updates/blogs/penn-physician-blog/2020/august/airborne-dropletdebate-article
The ridiculous belief in fomite-to-face being a primary mode of transmission led to the use of surface
disinfection protocols that wasted time, energy, productivity, and disinfectant:
https://www.nature.com/articles/d41586-021-00251-4
The 6-foot guidelines are absolutely useless. The minimum safe distance to protect oneself from an
aerosolized virus is to be 15+ feet away from an infected person, no closer. Realistically, no public transit
is safe:
https://www.medrxiv.org/content/10.1101/2020.08.03.20167395v1
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.epa.gov/sciencematters/epa-researchers-test-effectiveness-face-masks-disinfectionmethods-against-covid-19
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.healthline.com/health-news/leaky-vaccines-can-produce-stronger-versions-of-viruses072715
https://www.realclearscience.com/articles/2021/08/23/lets_stop_pretending_about_the_covid19_vaccines_791050.html
https://www.cdc.gov/media/releases/2021/s0730-mmwr-covid-19.html
https://www.businessinsider.com/cdc-fully-vaccinated-new-guidelines-wear-masks-indoors-delta-2021-
7?utm_source=yahoo.com&utm_medium=referral
All of the COVID-19 vaccines currently in use have undergone minimal testing, with highly accelerated
clinical trials. Though they appear to limit severe illness, the long-term safety profile of these vaccines
remains unknown:
https://www.jdsupra.com/legalnews/accelerated-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
https://coronavirus.dc.gov/sites/default/files/dc/sites/coronavirus/page_content/attachments/Cartoon
%20Explainer%20How%20the%20Moderna%20and%20Pfizer%20Vaccines%20Work.pdf
These vaccines were produced or validated with the aid of fetal cell lines HEK-293 and PER.C6, which
people with certain religious convictions may object strongly to:
https://www.health.nd.gov/sites/www/files/documents/COVID%20Vaccine%20Page/COVID19_Vaccine_Fetal_Cell_Handout.pdf
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:
https://mcusercontent.com/22e41db63deaf4a84be439c0f/files/6a33980b-683f-4ee4-67d4-
cc98dc7fcd37/20210601_Guide_to_COVID_19_vaccines_for_parents.pdf
https://rightsfreedoms.wordpress.com/2021/06/16/researcher-we-made-a-big-mistake-on-covid-19-
vaccine/
It is claimed by vaccine manufacturers that the vaccine remains in cells in the shoulder, and that SARSCoV-2 Spike produced and expressed by these cells from the vaccine’s genetic material is harmless and
inert, thanks to the insertion of prolines in the Spike sequence to stabilize it in the prefusion
conformation, preventing the Spike from becoming active and fusing with other cells:
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/
https://yurideigin.medium.com/lab-made-cov2-genealogy-through-the-lens-of-gain-of-functionresearch-f96dd7413748
SARS-CoV-2 Spike has a prion-like domain that enhances its infectiousness:
https://www.preprints.org/manuscript/202003.0422/v1
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0023664
The Spike S1 RBD may bind to heparin-binding proteins and promote amyloid aggregation. In humans,
this could lead to Parkinson’s, Lewy Body Dementia, premature Alzheimer’s, or various other
neurodegenerative diseases:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988450/
This is very concerning because SARS-CoV-2 S1 is capable of penetrating the blood-brain barrier and
entering the brain. It is capable of increasing the permeability of the blood-brain barrier to itself and
other molecules by injuring and disrupting it directly:
https://www.nature.com/articles/s41593-020-00771-8
https://www.nature.com/articles/s41392-021-00719-9
https://pubmed.ncbi.nlm.nih.gov/33053430/
SARS-CoV-2, like other betacoronaviruses, may have Dengue-like ADE, or antibody-dependent
enhancement of disease:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943455/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7454712/
https://www.journalofinfection.com/article/S0163-4453(21)00392-3/fulltext
https://sharylattkisson.com/2021/08/study-why-so-many-vaccinated-people-are-getting-sick/
https://www.nature.com/articles/s41564-020-00789-5
https://www.sciencedirect.com/science/article/pii/S1201971220307311
https://pubmed.ncbi.nlm.nih.gov/31826992/
https://www.biorxiv.org/content/10.1101/2021.08.22.457114v1
There is something called Original Antigenic Sin, which is the observation that the body prefers to
produce antibodies based on previously-encountered strains of a virus over newly-encountered ones:
https://www.jimmunol.org/content/202/2/335
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://news.unchealthcare.org/2021/06/scientists-discover-how-dengue-vaccine-fails-to-protectagainst-disease/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739535/
https://www.scientificamerican.com/article/how-the-worlds-first-dengue-vaccination-drive-ended-indisaster/
In mice immunized against SARS-CoV and challenged with the virus, a close relative of SARS-CoV-2, they
developed immune sensitization, Th2 immunopathology, and eosinophil infiltration in their lungs:
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0035421
We have been told that SARS-CoV-2 mRNA vaccines cannot be integrated into the human genome,
because messenger RNA cannot be turned back into DNA. This is false. There are elements in human cells
called LINE-1 retrotransposons, which can indeed integrate mRNA into a human genome by endogenous
reverse transcription:
https://pubmed.ncbi.nlm.nih.gov/33330870/
https://rightsfreedoms.wordpress.com/2021/08/13/mit-harvard-study-suggests-mrna-vaccine-mightpermanently-alter-dna-after-all/
https://home.solari.com/deep-state-tactics-101-the-covid-injection-fraud-its-not-a-vaccine/
The vaccine and the virus were made by the same people. In 2014, there was a moratorium on SARS
gain-of-function research that lasted until 2017:
https://www.phe.gov/s3/dualuse/documents/gain-of-function.pdf
https://www.scientificamerican.com/article/u-s-lifts-moratorium-on-funding-controversial-high-riskvirus-research/
https://www.nih.gov/about-nih/who-we-are/nih-director/statements/nih-lifts-funding-pause-gainfunction-research
Ralph Baric is a virologist and SARS expert at UNC Chapel Hill in North Carolina. This is who Anthony
Fauci was referring to when he insisted, before Congress, that if any gain-of-function research was being
conducted, it was being conducted in North Carolina:
https://sph.unc.edu/adv_profile/ralph-s-baric-phd/
https://alumni.unc.edu/news/ralph-baric-on-the-front-lines-of-coronavirus-for-three-decades/
Ralph Baric and Shi Zhengli are colleagues and have co-written papers together:
https://www.nature.com/articles/nm.3985/
Ralph Baric mentored Shi Zhengli in his gain-of-function manipulation techniques, particularly serial
passage, which results in a virus that appears as if it originated naturally. In other words, deniable
bioweapons. Serial passage in humanized hACE2 mice may have produced something like SARS-CoV-2:
https://www.technologyreview.com/2021/06/29/1027290/gain-of-function-risky-bat-virus-engineeringlinks-america-to-wuhan/
https://usrtk.org/biohazards-blog/ralph-baric-emails/
https://www.paul.senate.gov/newsweek-op-ed-congress-must-pursue-answers-about-origin-covid-19
https://nymag.com/intelligencer/article/coronavirus-lab-escape-theory.html
The funding for the gain-of-function research being conducted at the Wuhan Institute of Virology came
from Peter Daszak. Peter Daszak runs an NGO called EcoHealth Alliance:
https://peterdaszak.com/
https://peterdaszak.com/interceptdocs.pdf
https://theintercept.com/2021/09/09/covid-origins-gain-of-function-research/
https://nationalfile.com/bombshell-fauci-kept-funding-peter-daszaks-wuhan-gain-of-functionexperiments-with-7-5-million-after-trump-canceled-grant/
EcoHealth Alliance received millions of dollars in grant money from the National Institutes of
Health/National Institute of Allergy and Infectious Diseases (that is, Anthony Fauci), the Defense Threat
Reduction Agency (part of the US Department of Defense), and the United States Agency for
International Development. NIH/NIAID contributed a few million dollars, and DTRA and USAID each
contributed tens of millions of dollars towards this research. Altogether, it was over a hundred million
dollars:
https://www.independentsciencenews.org/wp-content/uploads/2020/12/EcoHealth-Funding-as-of01_10_2020-Fed.-Grants-Contracts.pdf
EcoHealth Alliance subcontracted these grants to the Wuhan Institute of Virology, a lab in China with a
very questionable safety record and poorly-trained staff, so that they could conduct gain-of-function
research:
https://www.algora.com/Algora_blog/2021/09/22/ecohealth-alliance-darpa-toyed-with-infecting-wildchinese-bats-with-covid-leaked-docs-allege
https://nypost.com/2021/07/01/pentagon-gave-millions-to-ecohealth-alliance-for-wuhan-lab/
https://www.judicialwatch.org/press-releases/wuhan-lab-fauci-grants/
https://www.judicialwatch.org/documents/jw-v-nih-wuhan-june-2021-00696/
https://scholar.harvard.edu/files/kleelerner/files/20200414_wapo_-
_state_department_cables_warned_of_safety_issues_at_wuhan_lab_studying_bat_coro naviruses_-
_the_washington_post.pdf
https://www.businessinsider.com/us-officials-raised-alarms-about-safety-issues-in-wuhan-lab-report2020-4?op=1
Chinese scientists in Wuhan reported being routinely bitten and urinated on by laboratory animals:
https://img-prod.tgcom24.mediaset.it/images/2020/02/16/114720192-5eb8307f-017c-4075-a697-
348628da0204.pdf
https://web.archive.org/web/20200214144447/https:/www.researchgate.net/publication/339070128_
The_possible_origins_of_2019-nCoV_coronavirus
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
https://thehill.com/policy/healthcare/556815-fauci-calls-on-china-to-release-medical-records-ofwuhan-researchers
December 12th, 2019, Ralph Baric signed a Material Transfer Agreement (essentially, an NDA) to receive
Coronavirus mRNA vaccine-related materials co-owned by Moderna and NIH:
https://rightsfreedoms.wordpress.com/2021/06/26/confidential-documents-reveal-moderna-sentmrna-coronavirus-vaccine-candidate-to-university-researchers-weeks-before-emergence-of-covid-19/
https://s3.documentcloud.org/documents/6935295/NIH-Moderna-Confidential-Agreements.pdf
It wasn’t until a whole month later, on January 11th, 2020, that China allegedly sent us the sequence to
what would become known as SARS-CoV-2:
https://www.cidrap.umn.edu/news-perspective/2020/01/china-releases-genetic-data-new-coronavirusnow-deadly
https://www.sciencedaily.com/releases/2020/01/200131114748.htm
Moderna claims, rather absurdly, that they developed a working vaccine from this sequence in under 48
hours:
https://www.businessinsider.com/moderna-designed-coronavirus-vaccine-in-2-days-2020-11
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://www.biomerieux.com/en/board-directors-biomerieux-chaired-alain-merieux-has-appointedstephane-bancel-directeur-general
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://www.fondation-merieux.org/en/news/alain-merieux-receives-the-prestigious-chinese-reformfriendship-award/
https://medicalxpress.com/news/2020-04-wuhan-lab-core-virus-controversy.html
http://english.whiov.cas.cn/ne/201712/t20171212_187624.html
https://web.archive.org/web/20210921133410/http://english.whiov.cas.cn/ne/201712/t20171212_187
624.html
The sequence given as the closest relative to SARS-CoV-2, RaTG13, is not a real virus. It is a forgery:
https://nerdhaspower.weebly.com/ratg13-is-fake.html
https://gnews.org/192144/
https://www.peakprosperity.com/forum-topic/scientific-history-of-ratg13/
The animal reservoir of SARS-CoV-2 has never been found:
https://www.technologyreview.com/2021/03/26/1021263/bat-covid-coronavirus-cause-origin-wuhan/
https://www.who.int/news-room/feature-stories/detail/how-who-is-working-to-track-down-theanimal-reservoir-of-the-sars-cov-2-virus
The FBI raided Allure Medical in Shelby Township north of Detroit for billing insurance for “fraudulent
COVID-19 cures”. The treatment they were using? Intravenous Vitamin C. An antioxidant. Which, as
described above, is an entirely valid treatment for COVID-19-induced sepsis, and indeed, is now part of
the MATH+ protocol advanced by Dr. Paul E. Marik:
https://www.freep.com/story/news/local/michigan/macomb/2020/04/28/allure-medical-spa-shelbycovid-vitamin-c/3038801001/
https://www.detroitnews.com/story/news/local/macomb-county/2020/05/15/doctor-got-loan-whilepeddling-phony-covid-19-cure-feds-say/5197315002/
https://covid19criticalcare.com/covid-19-protocols/math-plus-protocol/
https://covid19criticalcare.com/wp-content/uploads/2021/01/FLCCC-Alliance-MATHplus-ProtocolENGLISH.pdf
https://pubmed.ncbi.nlm.nih.gov/31978969/
https://www.sciencedirect.com/science/article/abs/pii/S0883944119316107?via%3Dihub
https://www.npr.org/sections/health-shots/2019/10/01/766029397/mixed-results-for-a-test-ofvitamin-c-for-sepsis
https://www.nutraingredients.com/Article/2020/01/28/Ethically-and-morally-unacceptable-Reactionto-vitamin-C-for-sepsis-trial
The FDA banned ranitidine (Zantac) due to supposed NDMA (N-nitrosodimethylamine) contamination:
https://www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press-announcements-ndmazantac-ranitidine
https://www.raps.org/news-and-articles/news-articles/2021/6/fda-studies-no-post-ingestion-ndmafrom-ranitidine
Ranitidine is not only an H2 blocker used as antacid, but also has a powerful antioxidant effect,
scavenging hydroxyl radicals. This gives it utility in treating COVID-19:
https://onlinelibrary.wiley.com/doi/10.1111/j.1472-8206.2009.00810.x
https://www.sciencedirect.com/science/article/pii/S1347861319342203
The FDA also attempted to take N-acetylcysteine, a harmless amino acid supplement and antioxidant, off
the shelves, compelling Amazon to remove it from their online storefront:
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warningletters/les-labs-593764-07232020
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-nacsupplements
On June 9th, 2020, Charles Lieber, a Harvard nanotechnology researcher with decades of experience, was
indicted by the DOJ for fraud:
https://www.justice.gov/opa/pr/harvard-university-professor-and-two-chinese-nationals-chargedthree-separate-china-related
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://www.science.org/news/2020/02/why-did-chinese-university-hire-charles-lieber-do-batteryresearch
https://news.harvard.edu/gazette/story/2012/01/reading-lifes-building-blocks/
https://news.harvard.edu/gazette/story/2019/07/harvard-researchers-present-nanowire-devicesupdate/
The indictment was over his collaboration with the Wuhan University of Technology. He had doubledipped, against the terms of his DOD grants, and taken money from the PRC’s Thousand Talents plan, a
program which the Chinese government uses to bribe Western scientists into sharing proprietary R&D
information that can be exploited by the PLA for strategic advantage (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.nytimes.com/2020/02/06/us/chinas-lavish-funds-lured-us-scientists-what-did-it-get-inreturn.html
https://www.nature.com/articles/d41586-020-00291-2
https://www.hsgac.senate.gov/imo/media/doc/2019-11-18%20PSI%20Staff%20Report%20-
%20China's%20Talent%20Recruitment%20Plans.pdf
https://www.research.psu.edu/sites/default/files/FBI_Risks_To_Academia.pdf
https://www.chinacenter.net/2020/china_currents/19-3/scholars-or-spies-u-s-china-tension-inacademic-collaboration/
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:
http://cml.harvard.edu/assets/Nanowire-probes-could-drive-high-resolution-brain-machineinterfaces.pdf
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/
https://cml.harvard.edu/assets/Cyborg-tissues_-Merging-engineered-human-tissues-with-biocompatible-nanoscale-wires.pdf
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.forbes.com/sites/giacomotognini/2020/11/12/mit-scientist-bob-langer-becomes-abillionaire-thanks-to-moderna-stock-rally/?sh=41c3819a3a90
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:
http://cml.harvard.edu/
https://langerlab.mit.edu/
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:
https://invesbrain.com/klaus-schwab-great-reset-will-lead-to-fusion-of-our-physical-digital-biologicalidentity/
https://www.penguinrandomhouse.com/books/598250/shaping-the-future-of-the-fourth-industrialrevolution-by-klaus-schwab-founder-and-executive-chairman-world-economic-forum-with-nicholasdavis/
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://ambassadorlove.wordpress.com/2021/08/09/confirmed-graphene-oxide-main-ingredient-incovid-shots/
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/
https://www.cbc.ca/news/canada/montreal/masks-early-pulmonary-toxicity-quebec-schools-daycares1.5966387
https://humansarefree.com/2021/04/bombshell-disposable-blue-face-masks-found-to-contain-toxicasbestos-like-substance-that-destroys-lungs.html
Japanese researchers have also found unexplained contaminants in COVID-19 vaccines:
https://www.nbcnews.com/news/world/japan-suspends-1-6m-doses-moderna-shot-aftercontamination-reports-n1277669
https://www.fiercepharma.com/pharma/contaminant-moderna-covid-19-vaccine-vials-found-japanwas-metallic-particles-report
https://www.theburningplatform.com/2021/08/27/japan-suspects-contaminant-in-moderna-vaccinesis-metallic-reacts-to-magnets/
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://www.templehealth.org/about/news/sars-cov-2-spike-proteins-disrupt-the-blood-brain-barrierpotentially-raising-risk-of-neurological-damage-in-covid-19-patients
https://www.croiconference.org/abstract/neuromodulatory-effects-of-sars-cov-2-on-the-blood-brainbarrier/
https://www.nature.com/articles/s41598-020-75253-
9?utm_source=xmol&utm_medium=affiliate&utm_content=meta&utm_campaign=DDCN_1_GL01_met
adata_scirep
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/
https://www.naturalnews.com/2021-07-19-graphene-based-neuromodulation-technology-is-realinbrain-neuroelectronics.html
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://neuralink.com/
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
https://www.psychologytoday.com/us/blog/the-future-brain/202107/ai-and-vr-transform-thoughtsaction-wireless-bci
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://www.adforum.com/agency/6664937/press-releases/70226/opinion-the-last-humans-and-thenext-brands
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.egonzehnder.com/de/insight/can-dark-triad-leaders-be-a-good-choice-for-a-leadershipposition
https://www.sakkyndig.com/psykologi/artvit/babiak2010.pdf
https://www.theatlantic.com/health/archive/2012/07/the-startling-accuracy-of-referring-to-politiciansas-psychopaths/260517/
https://medium.com/world-issues-politics-economics-and-more/the-rise-of-the-psychopath-andsociopath-to-political-power-b67ef9073477
https://fortune.com/2021/06/06/corporate-psychopaths-business-leadership-csr/
https://www.washingtonpost.com/news/on-small-business/wp/2016/09/16/gene-marks-21-percent-ofceos-are-psychopaths-only-21-percent/
https://www.forbes.com/sites/jackmccullough/2019/12/09/the-psychopathic-ceo/
https://en.wikipedia.org/wiki/Psychopathy_in_the_workplace

Call it aSparagus Letter.     8)

Well, I commented on bitunlocker’s thread with the Spartacus letter - which got deleted without even an email saying so.

Bump it baby!

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

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

Rumour has it the next one will be a highly transmissable MERS version. Could be just a rumour though 8)

the pedos aristo fascist terrorists want to keep their plunder at all costs (specially their sex slaves) and helped by the "inversers" would without problem wipe 99% of humanity... they are the real terros... and I guess cv1 was just a warning shot about their legal immunity regarding pedo activites... more and more... I believe that...

Rumour has it the next one will be a highly transmissable MERS version. Could be just a rumour though 8)

Apparently it’s already down. [refresh your cache]

In a perfect AI plandemic, this is the way to go - strategically wise.
Even that massive cunt Billy G has hinted that, and I would take the next outbreak very seriously indeed.

Death count will be the evidence, which is lacking in the current one.

---

Ooops, my bad, it’s still up!

I could not have imagined, that the University VPN/ip of the people I sent it to, was responsible to begin with.
Academic research institutions censoring their sheeple to the core, just wow.

[moderator's note: consecutive posts merged]

wow, first time I see a moderator note ever ! should we start to sign our message now?

Looks like "Spartacus" has some... problems:


A worldwide anti-incel conspiracy. Sounds totally legit.

So that’s what you acquired from all that, riiight. :P

He even supported his arguments with sources and links and facts. That's some hardcore shit I can tell just by looking at it.

He didn't really. He copy-pasted a bunch of loosely-related stuff that may or may not be factual but provided zero proof for the most far-reaching conclusions, like all that mind control nonsense.

I'd have thought bitcoiners would be sufficiently tech savvy to call out that BS on sight but apparently conspiratardery trumps technology 100% of the time.

I don't mean you specifically, mindrust - I know you're not a bitcoiner ;)

The world is ran by factions who occassionally argue among themselves. They have no interest in nation states,religion,gender,race with regards the common people. Take for example the EU.This sector is simply a means to an end but is controlled by one faction. In the end the world will be approx 10 regions under the control of various factions. Today the earths resources are literally owned bought and paid for (using debt based instruments) by each faction through private trusts within large hedge funds. (NOT the unsecured investard type) Legacy trusts. Think the ivy league of the investor class. Same the world over. Russia is controlled by a few peope, China is controlled by a few people. The US is the same. Forget about political whores class types.These people are way beyond laws of nation states and collaborate to create a world order where they can NEVER be usurped.

He didn't really.

He copy-pasted a bunch of loosely-related stuff ~

~ that may or may not be factual  ~

but provided zero proof for the most far-reaching conclusions, like all that mind control nonsense.

I'd have thought bitcoiners would be sufficiently tech savvy to call out that BS on sight ~

~ but apparently conspiratardery trumps technology 100% of the time.

I don't mean you specifically, mindrust - I know you're not a bitcoiner ;)

We may have a slight mistrust for TPTB, especially when it comes to censoring speech..
(BTC is speech)   

....
He probably is a bitcoiner, and he’s full of shit - much like you are.

Oh noes, sugar got me on ignore, what-am-I-going to do? :'(

Damn, the flat earth thread was way more fun wasn't it?

He probably is a bitcoiner, and he’s full of shit - much like you are.

Oh noes, sugar got me on ignore, what-am-I-going to do? :'(

I am a bitcoiner and I don't think I am full of shit.

This topic got all the usual suspects buzzing.  Just like touching a bee-hive or ant-hill.  Visibly upsetting the 'hive mind' is a pretty good marker that there is something worth evaluating with a slightly elevated level of effort.

And again, censorship is another good reason.

Speak for yourself, Greek man.

Damn, the flat earth thread was way more fun wasn't it?

eat shit and die?

I am a bitcoiner and I don't think I am full of shit.

You can start by not quoting her.

Do you really like to read a sjw/commie/liberal propaganda machine so much?

Sorry buddy, but the timing of the “mindrust event” is a hard pill to swallow.

I can’t help it. I do try to keep my sexual desires for her at bay however.

Do you really like to be bullied out of the life you thought you had?
I despise the MSM that choke their narrative down your throat, to the point of brainwashing the few brain cells that are still working.

I am fully behind my decision even if it was wrong. It may become right eventually.

I don't understand why anybody else bothers with it other than me.

The time will tell who was right, eventually.

According to yourself, you’ve lost around $500k USD in realised/un-realised profits in the last 18 months.
How can this become right - eventually? :P

The freaking timing (March 2020) - on WO.

When the AI plandemic broke out last year, we couldn’t have this discussion - due to the lack of data. It’s not the case anymore.

If, and that's one BIG IF, btc goes from $60k to 0, ~

~ it will make me look like a genius.

...

All in all, I give it 2/10 for accuracy of the content, but 10/10 for knowing his audience won't read, understand, or really even care about the accuracy of the content.

I suppose we all have to listen to that mobster Dr. Fauci, and never question authority instead, right?

I don't really care what any one individual, Fauci included, says. I care about what the overwhelming consensus of evidence says, which is that vaccines work and that this letter is bull.

In a perfect AI plandemic, this is the way to go - strategically wise.

Yup.  All the people involved in the plandemic fraud and all the people who will profit from it agree;  get injected with the gene therapy because it works perfectly and there are zero problems.  It's a Consensus!

I don't really care what any one individual, Fauci included, says. I care about what the overwhelming consensus of evidence says, which is that vaccines work and that this letter is bull.

Can you please stop hijacking the topic? I don't really care what you or anyone else thinks about my trades.

I already have a lot of people on ignore and I'll have to add another one if you keep doing this.

I don't really care what any one individual, Fauci included, says. I care about what the overwhelming consensus of evidence says, which is that vaccines work and that this letter is bull.

The overwhelming consensus of propaganda is that vaccines “work”, depending on your definition of “work”, and depending on the (ever changing) definition of “herd immunity”..

Vaccines “work: Ok, I’ll accept the fact that they “work” if you consider their only benefit, of likely/possibly reducing the severity of Covid infection/symptoms..

Do these “vaccines” provide immunity? NO!
Will they contribute to “herd immunity”? NO! (Because they don’t even provide immunity)
Do they prevent infection? NO!
Do they prevent you from spreading? NO!!

Do these “vaccines” provide immunity? NO!
Will they contribute to “herd immunity”? NO! (Because they don’t even provide immunity)
Do they prevent infection? NO!
Do they prevent you from spreading? NO!!

If anything, the vaccines are causing the vaccinated to spread it around MORE, walking around contagious without any symptoms, being free from wearing masks even though they can and do still spread it..

Herd immunity?

Vaccines safe?
Their are MOUNTAINS of evidence to the point that the vaccines are at the very least not 100% safe (or effective)..

Knowing all these FACTS, how can you still parrot the mainstream propaganda narrative?

Where are you atleast willing to meet in the middle at all?

I'm not parroting anything.

I'm critically appraising the evidence for myself and reaching the only logical conclusion.

It's not a case of meeting in the middle when one side has facts and evidence and the other side has only conspiracy theories and baseless speculation.

Provide evidence that my views are wrong and I will change them. It's as simple as that.

I don’t impose my opinion to others, so I don’t like it if they do.

Hanging around on a discussion forum probably isn't a great idea then.

In terms of the actual content, the author has designed the letter quite smartly knowing full well that the vast majority of conspiracy nuts won't read it, and the parts that they do read, they won't understand so will just accept what he has said is true. He starts off stating mostly accurate facts with good references to scientific studies about how COVID attacks almost every body system, causing widespread organ failure, to lure people in to thinking he knows what he is talking about. (But I thought it was just a flu? Or according to some, it doesn't even exist? So it is a deadly disease now that you think it suits your agenda? Gotcha.)

By the time he gets on to talking about treatments, he knows most of his audience won't be checking the references (if they ever did to begin with). For example, his reference for the statement that intubation is what kills these patients - https://www.nature.com/articles/pr2009174 - is a vaguely related paper published in 2009 that has absolutely nothing to do with COVID at all. Out of his three links for this statement - "The correct treatment for severe COVID-19 related sepsis is non-invasive ventilation, steroids, and antioxidant infusions" - only one of them talks about ventilation and clearly states that intubation is necessary.

A delicate balance exists between ROS production and the antioxidant defenses that protect cells in vivo. This balance may become disturbed under conditions of hyperoxia, inflammation, or ischemia-reperfusion (excessive generation of ROS) or in the presence of limited or impaired antioxidant defenses.

The rest of this section follows the same theme, with him either not referencing sections which are purely speculation, using references which do not support his claims as above, or in some cases, using references which actively disprove his claims, such as one of his references "supporting" ivermectin - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539925/ - which clearly states "The antiviral activity of ivermectin has not been consistently proven in vivo." (In vivo means in living organisms).

By the time we get to all the insane ramblings about it being a criminal conspiracy, the author has abandoned all pretense of providing credible references, instead linking a bunch of news articles, blog posts, and right wing conspiracy sites such as https://rightsfreedoms.wordpress.com and https://www.thelibertybeacon.com.

95% reduction in infection - https://www.acpjournals.org/doi/10.7326/M21-1577
90% reduction in infection - https://www.bmj.com/content/373/bmj.n888
94% reduction in hospitalization - https://www.cdc.gov/mmwr/volumes/70/wr/mm7018e1.htm
50% reduction in transmission - https://khub.net/documents/135939561/390853656/Impact+of+vaccination+on+household+transmission+of+SARS-COV-2+in+England.pdf/35bf4bb1-6ade-d3eb-a39e-9c9b25a8122a?t=1619601878136

I am Spartacus. I can answer any questions you may have.


Most people who claim that COVID-19 is "just a flu" do not understand the disease even remotely and have made no effort to study the underlying pathophysiology. Hyperinflammatory COVID-19 that puts people in the ICU is basically sepsis. It has been shown that sepsis can be treated with antioxidants, like intravenous Vitamin C (see the MATH+ protocol for COVID-19, as well as papers regarding the repurposed drugs - fluvoxamine, budesonide, famotidine, and so on - and their antioxidant activity).

Ultimately, the damage of COVID-19 is caused by lipid peroxidation, where electrons are stripped from fats in the body, causing them to become oxidized. As a matter of fact, COVID-19's pathology is somewhat unique among viruses in the sense that immune over-activation and free radical damage is a primary mechanism of injury. It is very likely that it shares this trait with SARS, however.


Read it again.


COVID-19 down-regulates Nrf2, impairing antioxidant defenses. This means that the enzymes your phagocytes (neutrophils, etc.) use to attack pathogens start digesting your own cells with peroxide and bleach instead.

Ischemia causes a buildup of hypoxanthine, succinate, et cetera, that form superoxide radicals when O2 is reintroduced and these substances begin breaking down by their enzymatic pathways. This is called ischemia-reperfusion injury.

What those "unrelated" documents show, to a thorough reader, is that shocking hypoxic cells with oxygen causes lipid peroxidation by reperfusion.

Since the virus already causes lipid peroxidation, this merely layers even more lipid peroxidation atop lipid peroxidation, causing the tissues in the lungs to basically dissolve.

COVID-19 patients have blood that is chemically incapable of transporting oxygen due to a buildup of hypochlorous acid that is stripping iron out of their heme and competing for O2 binding sites. What this means is that they will suffer from "silent" hypoxia, where they appear to be breathing just fine, but are suddenly turning blue in the face as their red blood cells chemically refuse to carry O2.

This has been directly observed in COVID-19 patients.

Pumping O2 into the lungs does not make RBCs chemically incapable of carrying O2 somehow magically capable of carrying it. All it does is produce more ROS injury.

By the way, all this iron stripped out by hypochlorous acid is reactive, and forms deadly hydroxyl radicals that oxidize the lining of blood vessels through the Haber-Weiss and Fenton chemical reactions with hydrogen peroxide and superoxide.

Proning and venting without scavenging radicals will 100% kill people. The radicals strip electrons from phospholipids, PUFAs, cholesterol, cardiolipin, DNA, anything within reach. The oxidized lipids cause a feedback loop of inflammation and autoimmunity by triggering pattern recognition receptors. Look up what "damage-associated molecular patterns" means.

These people are dying of something that's sort of like lupus and rheumatoid arthritis going off simultaneously in the lining of their vascular system. It is a virus that triggers an autoimmune syndrome akin to sepsis, but strangely without any shock and accompanying loss of blood pressure, in many cases.


The majority of clinical trials of antivirals (any antivirals, not just Ivermectin) enroll people who have no virus left in their bodies. That is, hospitalized patients. Then, they idiotically claim that these antivirals don't shorten the length of hospital stays.

Why don't they shorten the length of hospital stays? Because there is no virus left in the patients' bodies.

Google it. Go to Google Images, and put in COVID-19 clinical course. They all show the same thing. Peak viral load occurs right around when someone becomes symptomatic. By the time hyperinflammation sets in about 5 to 7 days later, the viral load has tapered off to almost nothing.

Using antivirals on people who have no virus in their bodies is not only futile, it tells us nothing about their prophylactic effects, if any.

Many of the concerns raised about the vaccine have been corroborated (in far greater detail) by Stephanie Seneff:

https://dpbh.nv.gov/uploadedFiles/dpbhnvgov/content/Boards/BOH/Meetings/2021/SENEFF~1.PDF


Read the sources and the leaked documents within.

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

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

Ralph Baric signed a Material Transfer Agreement that showed he took delivery of Coronavirus mRNA vaccine-related materials co-owned by NIH and Moderna on December 12th, 2019, practically a whole month before we were sent the sequence to SARS-CoV-2 (a.k.a. 2019-nCoV), on January 11th, 2020. Moderna claims they made a vaccine from that sequence two days later, on January 13th. But as the MTA shows, Moderna already had a vaccine for an unspecified coronavirus a whole month earlier, before an outbreak was even announced. This is incredibly suspicious.

Stephane Bancel, the CEO of Moderna, previously worked for Alain Merieux's company, bioMerieux. Alain Merieux is a buddy of the CCP and helped them build the WIV's P4 laboratory.

The NIH/NIAID, DTRA, and USAID contributed over a hundred million dollars to Peter Daszak's EcoHealth Alliance NGO. EcoHealth Alliance subcontracted these grants to the Wuhan Institute of Virology for them to conduct gain-of-function research on bat coronaviruses, in violation of the 2014 moratorium on federal funding for SARS GOF research (essentially, Anthony Fauci and the NIH ignored the moratorium, offshored the research to China, and laundered the money through EcoHealth Alliance).

https://peterdaszak.com

As for the neural lace stuff, this is not just hypothetical, nor is it science fiction. It is very much real.

https://www.youtube.com/watch?v=N02SK9yd60s

James Giordano's files show that nanoparticles can be used to influence brain activity, and explicitly describes their use by hostile foreign powers to target civilians and use them to change mood, behavior, et cetera, in such a way as to damage society and cause chaos.

SARS-CoV-2 Spike makes the BBB more permeable, which would assist nanoparticles in crossing it.

Robert Langer, the cofounder of Moderna, was a colleague of Charles Lieber and co-wrote a paper with him.

https://www.bostonglobe.com/2020/01/28/metro/harvard-scientists-arrest-stuns-colleague/

Charles Lieber is a bionanotechnology expert at Harvard whose papers describe brain-computer interfaces made with nanoparticles.

Charles Lieber was arrested for douple-dipping and taking money both from DARPA and from the Wuhan University of Technology, under China's R&D-headhunting Thousand Talents Plan.

https://www.justice.gov/opa/pr/harvard-university-professor-indicted-false-statement-charges

DARPA has a program called the BRAIN Initiative, as well as the N3 program, the explicit goals of which are to develop non-invasive or minimally-invasive injectable nanoparticle BCIs, a.k.a. "Neural Laces", for disabled soldiers to control prosthetics, or for supersoldiers to control drones, and so forth.

https://www.darpa.mil/news-events/2019-05-20

The vaccine has been found by independent researchers to contain unknown nanoparticles.

https://www.orwell.city/2021/06/la-quinta-columna-5G-graphene-oxide-and-neuro-rights.html

Even though I marked that particular section of the letter as speculative, and it is, it is certainly the case that all of these things, taken together, constitute more than enough circumstantial evidence to, at the very least, raise the alarm.

SARS-CoV-2 Spike makes the BBB more permeable, which would assist nanoparticles in crossing it.

Robert Langer, the cofounder of Moderna, was a colleague of Charles Lieber and co-wrote a paper with him.

https://www.bostonglobe.com/2020/01/28/metro/harvard-scientists-arrest-stuns-colleague/

I am Spartacus.

Even though I marked that particular section of the letter as speculative, and it is, it is certainly the case that all of these things, taken together, constitute more than enough circumstantial evidence to, at the very least, raise the alarm.

Holy smokes, we’re we able to summon the REAL Spartacus here to bitcointalk?

Spartacus, this is a free speech board, you should absolutely be able to post/publish anything you want here and feel secure that it was not a waste of your time.. This IS a good place for you..

I saw your letter being removed left and right everywhere I searched and thought to repost it here in full as I knew this would be a safe sanctuary..
(Someone tried deleting one on technical grounds but was foiled)

This website is wealthy beyond reason and holds freedom of speech to the highest degree.. It will battle nations for our right to speak our minds I am sure..

If you have ANY deleted posts here, you let me know and I will go to battle here for this principle, or directly contact the administrator theymos..

Read the rules (that have nothing to do with censorship) and you will be free to record anything you want here..

I also have a question..
What do we do now?
If all you say is true, then what is the path forward?

Excuse my cherry picking - but this grabbed my attention. For all the microchip talk or nanoparticle talk, none have described and mechanism at which how the vaccines cause any damage. So you believe through Dr. Lieber's work, there are nanoparticles that create perforations in the BBB, causing the nanoparticles to attach itself in the brain and allow for remote control?

And so, where in Dr. Liber's research specifically, what paper, do you have that provides evidence of this?

Did he sell all this info to china and no public records exists of how far advanced his research goes? This would not be the giant conspiracy that it may seem, because the Chinese are always ripping the top labs in the world so they don't have to produce the cash to fund R&D. In this case, there was collusion. Perhaps slightly more sinister, but China does this in all fields.

Since joining Battelle in 2011, Gaurav has served as the technical lead or lead investigator on a number of cutting-edge projects involving peripheral nerve stimulation, spinal cord stimulation and brain-computer interfaces. He was also the lead investigator for the Blood-Brain Barrier (BBB) engineering program, a Defense Threat Reduction Agency (DTRA)-funded project aimed at developing nanotechnology-based strategies for delivery of drugs to the brain.

In contrast, minutely invasive technologies allow scientists to deliver nanotransducers without surgery: for example, an injection of a virus carrying light-sensitive sensors, or other chemical, biotech, or self-assembled nanobots that can reach individual neurons and control their activity independently without damaging sensitive tissue. The proposed use for these technologies isn’t yet well-specified, but as animal experiments have shown, controlling the activity of single neurons at multiple points is sufficient to program artificial memories of fear, desire, and experiences directly into the brain.

Snip

You can always join the rebellion against these tyrants and tell them to go fuck themselves. It is not really that hard.
Dump your big house that eats away half of your monthly income, get a smaller car, eat less and you'll be able to survive through this mess even without a job.
If you want to comply because you don't want to move from your comfort zone, then get ready to be vaxxed forever and end up a genetically modified bio-mess.

I am Spartacus. I can answer any questions you may have.

We shall bathe in Romans blood.

https://twitter.com/EliseiNicole/status/1442878794520539140

https://i.imgur.com/S2bOIS9.png


So much for a working vaccine.

Proof?

There is no evidence whatsoever, circumstantial or not.

You haven't shown any proof that this mind control stuff exists, or that it can be delivered with the vaccine, let alone that this was is actually happened.

Someone hypothesized something and someone funded some research.

You could equally successfully argue that the vaccine contains a fusion reactor or a wormhole.

And let's face it, without the mind control nonsense, all you've shown is that COVID-19 is quite dangerous, which... no shit, Sherlock.

Get vaccinated.

Yes. As a matter of fact, I have the latest versions of the docs:

ICENI Mission Statement: https://mega.nz/file/LIdixBwY#3sv5b0saEvZ6vsHpQuRBMCc84-08uvIfFYdcxUtYx9U
Spartacus Letter V2: https://mega.nz/file/HZNmyRKB#xF15FrsAEZkwBPi4tdUP5toBBqeRHDJJAHzZt6Hg_Qg
Spartacus Letter URLs: https://mega.nz/file/HIdCxJoL#ru6yOS3Fap9rBdcdR-Twxwfm0tX8-44TN4ztoYpC5yc
...

Talk about cherry picked data...

Most people who claim that COVID-19 is "just a flu" do not understand the disease even remotely and have made no effort to study the underlying pathophysiology. Hyperinflammatory COVID-19 that puts people in the ICU is basically sepsis. It has been shown that sepsis can be treated with antioxidants, like intravenous Vitamin C (see the MATH+ protocol for COVID-19, as well as papers regarding the repurposed drugs - fluvoxamine, budesonide, famotidine, and so on - and their antioxidant activity).

There are no controlled trials that have definitively demonstrated a clinical benefit for vitamin C in critically ill patients with COVID-19, and the available observational data are inconclusive.

We found no evidence of a reduced risk of COVID-19 outcomes among hospitalized COVID-19 patients who used famotidine compared with those who did not or compared with PPI or hydroxychloroquine users.

COVID-19 patients have blood that is chemically incapable of transporting oxygen due to a buildup of hypochlorous acid that is stripping iron out of their heme and competing for O2 binding sites. What this means is that they will suffer from "silent" hypoxia, where they appear to be breathing just fine, but are suddenly turning blue in the face as their red blood cells chemically refuse to carry O2.

This has been directly observed in COVID-19 patients.

Pumping O2 into the lungs does not make RBCs chemically incapable of carrying O2 somehow magically capable of carrying it. All it does is produce more ROS injury.

The majority of clinical trials of antivirals (any antivirals, not just Ivermectin) enroll people who have no virus left in their bodies.

Owing to very low certainty of evidence, the effect of ivermectin, compared with standard care, in reducing the risk of suspected, probable, or laboratory confirmed infection remains very uncertain; the certainty of evidence was rated down because of serious risk of bias and very serious imprecision.

Many of the concerns raised about the vaccine have been corroborated (in far greater detail) by Stephanie Seneff:

https://dpbh.nv.gov/uploadedFiles/dpbhnvgov/content/Boards/BOH/Meetings/2021/SENEFF~1.PDF

...

Interesting how o_i_l_e_o now all of a sudden has all the respect for the guy and is, however lamely, trying to address actual points rather than just spewing the random insults which work well with the personna's core groupies.

It's almost like a higher pay-grade someone in the next cube who can actually do 'science' with a little bit more of a credible facade took over the reigns of the Oileo account for a while.  More support for the hypothesis that there is a 'there there' to a lot of the stuff in the Spartacus docs and the social media influencer troll-farm hive insects are assigned to these part of the terrain are a bit nervous about it.

They are panicking right now.

-snip-

If my data are cherry picked, then where are all the data showing that vaccines don't work?

---

The MATH+ protocol is written by a scan organization, provides no data to support their recommendations, and is headed by individuals with vested interests in the fake treatments they recommend. Looking at the treatments they and you are suggesting:

Vitamin C:

Fluvoxamine:
No evidence. Biggest ongoing trial to date (https://clinicaltrials.gov/ct2/show/study/NCT04668950) has just reported "No treatment effect" on early results.

Famotidine:

Budesonide does have some evidence, but it is inferior to IV dexamethasone which we have been using for all our inpatients for months.

The links in your original letter consider these drugs in the context of rodent peptic ulcers, among other things. Hardly applicable to humans with COVID.

---

There's some truth in this, but not to degree you state. If there was enough hypochlorous acid to destroy hemoglobin to such a degree, why do we not see a severe hyperchloremic acidosis? Why do we not see buffer systems being completely overwhelmed? Why do we not see profound anemia due to hemoglobin destruction? Why does intubation and proning make the SpO₂ go from 70% to 95%? Why does it make the PaO₂ go from 60 mm Hg to 120 mm Hg?

Trying to claim that intubation and ventilation is actively killing people is just plain incorrect.

---

OK, so show me the randomized control trials which show ivermectin is an effective prophylactic. There is currently no evidence for this either:

I'm happy consider any treatment provided there is some evidence it works. You have failed to provide that evidence.

---

An article written by a computer scientist and a practitioner of "energy medicine", published in a fake journal which is not listed in PubMed, has no publisher, has literally zero impact factor, which is ran by a young Earth creationist and a lawyer who sues vaccine companies on behalf of "victims". And even then, they still state "there are no studies demonstrating definitively that this is happening". ::)

Come on. You seem smart enough to realize just how disingenuous and dishonest something like this is.

And the rest of your links go the same way as this one, and the same way as your original letter - off the deep end of conspiracy theories with absolutely no supporting evidence or facts.

....................
why over rule the 15 experts?
https://bitcointalk.org/index.php?topic=5362774.msg58051802#msg58051802

Lol, self.moderated thread with experts, i piss myself.

Shit philipma, I had not noticed, until I saw Bob’s reply.
How the fuck is the WO-gang experts at medicine? Maybe for meme’s and dildo stuff related, but that’s about it.

i piss myself.

nuff said.
Let mum change your diaper and then GTFO in the name of seriousness  ::)

Lol, self.moderated thread with experts, i piss myself.
Scientists and experts can be found in sig.

One liar down, lots to follow https://youtu.be/QZjeBxM2nOg?t=338

You have a point. Self-mod threads are for pussies. One does create self-modded threads only if he/she is afraid of what people might say. I try to never comment in these threads and I am not in favor of creating them.

Why even create a thread If you don't want certain people to certain stuff? Just have a telegram group...

pussies

.............
 That thread is for the hat gang,

If my data are cherry picked, then where are all the data showing that vaccines don't work?

The MATH+ protocol is written by a scan organization, provides no data to support their recommendations, and is headed by individuals with vested interests in the fake treatments they recommend. Looking at the treatments they and you are suggesting:

Vitamin C:

Fluvoxamine:
No evidence. Biggest ongoing trial to date (https://clinicaltrials.gov/ct2/show/study/NCT04668950) has just reported "No treatment effect" on early results.

Budesonide does have some evidence, but it is inferior to IV dexamethasone which we have been using for all our inpatients for months.

The links in your original letter consider these drugs in the context of rodent peptic ulcers, among other things. Hardly applicable to humans with COVID.

There's some truth in this, but not to degree you state. If there was enough hypochlorous acid to destroy hemoglobin to such a degree, why do we not see a severe hyperchloremic acidosis?

Why do we not see profound anemia due to hemoglobin destruction?

Why does intubation and proning make the SpO₂ go from 70% to 95%? Why does it make the PaO₂ go from 60 mm Hg to 120 mm Hg?

Trying to claim that intubation and ventilation is actively killing people is just plain incorrect.

Overproduction of oxidants and decrease in antioxidants lead to oxidation changes and cross-linking of proteins, lipids, DNA, and carbohydrates, deterioration of cell structures and their function, increased endothelial permeability and lung oedema formation, pulmonary epithelial dysfunction with impaired sodium ion transport and fluid reabsorption from the alveoli etc. [12]. In addition to intrinsically generated oxidants derived from phagocytic cells (recruited neutrophils and residential lung macrophages) and alveolar epithelial and endothelial cells [13], additional important source of oxidants is an inhalation of high oxygen concentrations used for mechanical ventilation of patients with severe ARDS [14].

Ferroptosis can be classified into canonical and non-canonical types to date. Canonical ferroptosis is started with the failure of glutathione peroxidase (GPX4) defense, leading to excessive lipid peroxidation and cell death18. Inactivation of GPX4 and glutathione (GSH) depletion play a central role in the induction of canonical ferroptosis18,19. Iron (II) oxidizes lipids in the Fenton reaction (hydrogen peroxide, iron and lipid) is the hallmark feature of ferroptosis, thereby generating lipid ROS, causing cell membrane damage17,18,19. GPX4 eliminates lipid ROS by consuming GSH and protects cell membrane against lipid peroxidation and ferroptosis18. Moreover, cystine/glutamate transporter (xCT) is responsible for providing cystine to produce GSH for GPX4 to function normally. Iron is an important metal in cells. But there is no efficient mechanism for excreting iron in the human body and, as a result, iron homeostasis is vulnerable to stresses.

Since the WHO declared COVID-19 a pandemic, a great effort has been made to understand this serious disease. Thousands of studies are being devoted to understanding its epidemiology, its molecular characteristics, its mechanisms, and the clinical evolution of this viral infection. However, little has been published on its pathogenesis and the host response mechanisms in the progress of the disease. Therefore, we propose a hypothesis based on strong scientific documentation, associating oxidative stress with changes found in patients with COVID-19, such as its participation in the amplification and perpetuation of the cytokine storm, coagulopathy, and cell hypoxia. Finally, we suggest a therapeutic strategy to reduce oxidative stress using antioxidants, NF-κB inhibitors, Nrf2 activators, and iron complexing agents. We believe that this hypothesis can guide new studies and therapeutic strategies on this topic.

To determine NO-derived oxidants, we measured systemic levels of nitrotyrosine in the plasma from healthy controls and COVID-19 patients (Fig. 5). Nitrotyrosine levels were significantly higher among patients with COVID-19 compared to healthy controls (107.049 ± 7.907 nM vs 44.7606 ± 12.85 nM; P<0.0001; Fig. 5A). Analysis by race showed a significant increase in nitrotyrosine levels both in Caucasian COVID-19 patients (108.2 ± 13.62 nM vs 48.54 ± 16.92 nM; p = 0.01; Fig. 5B), and in African Americans COVID-19 patients (106.2 ± 10.01 nM vs 40.69 ± 22.01 nM; p = 0.006; Fig. 5C) compared to respective race matched controls.

OK, so show me the randomized control trials which show ivermectin is an effective prophylactic. There is currently no evidence for this either:

I'm happy consider any treatment provided there is some evidence it works. You have failed to provide that evidence.

Figure 1. Course of COVID-19 and clinical benefits of antivirals. Following an incubation period of 3–6 days, SARS-CoV-2 infection generates a broad spectrum of clinical manifestations ranging from asymptomatic infection and mild illness to severe disease with high mortality. Viral load peaks around the day of symptom onset and rapidly declines thereafter. Accordingly, antiviral drugs like remdesivir (RDV) will only be effective early in infection when the number of new cells that become infected is still high. Antibody levels increase gradually and are commonly detectable after 7–14 days. Excessive immune responses, which may be curtailed by immunosuppressive agents like corticosteroids, lead to organ damage, intensive care admission, or death. Adopted from [19].

An article written by a computer scientist and a practitioner of "energy medicine", published in a fake journal which is not listed in PubMed, has no publisher, has literally zero impact factor, which is ran by a young Earth creationist and a lawyer who sues vaccine companies on behalf of "victims". And even then, they still state "there are no studies demonstrating definitively that this is happening". ::)

Come on. You seem smart enough to realize just how disingenuous and dishonest something like this is.

We show that intravenously injected radioiodinated S1 (I-S1) readily crossed the blood-brain barrier in male mice, was taken up by brain regions and entered the parenchymal brain space.

The post-infection of COVID-19 includes a myriad of neurologic symptoms including neurodegeneration. Protein aggregation in brain can be considered as one of the important reasons behind the neurodegeneration. SARS-CoV-2 Spike S1 protein receptor binding domain (SARS-CoV-2 S1 RBD) binds to heparin and heparin binding proteins. Moreover, heparin binding accelerates the aggregation of the pathological amyloid proteins present in the brain. In this paper, we have shown that the SARS-CoV-2 S1 RBD binds to a number of aggregation-prone, heparin binding proteins including Aβ, α-synuclein, tau, prion, and TDP-43 RRM. These interactions suggests that the heparin-binding site on the S1 protein might assist the binding of amyloid proteins to the viral surface and thus could initiate aggregation of these proteins and finally leads to neurodegeneration in brain. The results will help us to prevent future outcomes of neurodegeneration by targeting this binding and aggregation process.

And the rest of your links go the same way as this one, and the same way as your original letter - off the deep end of conspiracy theories with absolutely no supporting evidence or facts.

SARS-CoV-2 has non-human reservoirs and is now endemic. It will never go away. Period. It cannot be eradicated by vaccination, and anyone telling you it can be straight-up eradicated like smallpox with a high level of vaccination is lying. The current agenda of boosters will lead, inevitably, to bi-yearly shots, because the vaccine antibodies are waning within 6 months.

It has previously been suggested that antioxidants are useful for treating sepsis, because sepsis involves the over-activity of pro-oxidant enzymes that the body uses to fight infection.
...
It is entirely possible that COVID-19 hyperinflammation is, much like Keshan disease, a disease of low antioxidant capacity (redox equilibrium issues in the body due to chronic oxidative stress, i.e., endothelial dysfunction) that can be counteracted by raising levels of antioxidant substrates, such as selenium, glutathione, et cetera.

It's not conclusive proof of therapeutic effect, but it does point towards a fresh avenue of study.

I said, in the letter, that it was a catch-22, because you need oxygen to live. Intubation does increase oxygenation, but also causes VILI-like damage and additional oxidative stress alongside that.

Make no mistake, intubation will kill people who have COVID-19.

Pumping O2 into the lungs does not make RBCs chemically incapable of carrying O2 somehow magically capable of carrying it.

Early and proactive use of antioxidants, steroids, and non-invasive ventilation would likely render intubation pointless.

These studies virtually all enroll people who have COVID-19 hyperinflammation, have been symptomatic for around a week or more, and have been hospitalized.

I don’t impose my opinion to others, so I don’t like it if they do.

 Excuse me, ser, but do you have any self awareness?

 Like, even just a smidge?

 That thread is for the hat gang, WO regulars, and other folk that are capable of sexually pleasuring themselves by their own hand.

 Unlike you, with wrists so fucking weak, you dump all your bags in a panic, at the lowest point in 3 (?) years, and haven't shown your face in the WO thread since in shame.

 Go and sodomize yourself with a length of rusted pipe you fucking loser.

 Have fun staying poor.

So why bring it here. It has nothig to do here, stay in your encavement.

Muahahaha! Had a good laugh  ;D ;D ;D  Guys, just browse this troll's post history, he's so full of shit...  8)

Well said! This guy has no right to call anybody pussies well, apart from actual pussies i.e. female genitalia  ;D

Bob, this is not the place, nor the time, so kindly fuck off with the off-topicness.

The vaccines can be modified to target the Delta variant. Billions of people get yearly flu shots, which are modified every year, without any adverse effects.

This next section you have written includes a lot of speculation. Yes, we know COVID causes sepsis. Yes, we know that sepsis create a lot of reactive oxygen species and free radicals. So we speculate that treating with anti-oxidants would help. But every reputable large study (as I linked to in my previous post) we have on this issue has shown no benefit with antioxidant treatments.

Obviously I agree that people should stay fit and healthy, and if you want to take a vitamin C supplement, then knock yourself out. But we have no evidence that it (or other antioxidants) are an effective treatment for critically ill patients.

I'm not denying the cycle of NETosis, hypochlorous acid, and heme destruction. And I'm also not denying the existence of VALI/VILI, which is well described in the literature. But you also made the following two statements:


Yes this cycle happens, but not to such a degree that there is no functioning hemoglobin and that intubation and ventilation will not save the life of a critically hypoxic patient. To claim otherwise is dangerously wrong.

We do this already. Everyone who comes through the door gets dexamethasone and remdesivir pretty much immediately. If they require HFNO or NIV they also get tocilizumab. Intubation is always a last resort. You can see national treatment guidelines here:

The meta-analysis I linked in my previous post (https://www.bmj.com/content/373/bmj.n949) examined ivermectin and hydroxychloroquine as both pre- and post-exposure prophylaxis, and found no evidence of efficacy for either drug.

I'm not entirely sure what points you are trying to make with your section regarding the vaccine (even ignoring your obvious conspiracy nonsense at the bottom). If you are worried about the vaccine producing the S1 subunits, then what do you think happens with an active COVID infection? If you are worried about the spike protein itself, then why would you not want to avoid the cascade of it you would get with a COVID infection, which is several orders of magnitude higher than what you would get with a vaccine? I mean, the quote that you shared even specifically says "post-infection of COVID-19 includes a myriad of neurologic symptoms including neurodegeneration". Why would you not want to avoid this by taking the vaccine?

@Spartacus

I have seen some literature about how Nicotine stops other things from bonding to ACE receptors and that it could be a good counter to Covid..
Would you have any comments about that?

What about alcohol? As in recreational alcohol consumption.. What if any effect could you see that having on a Covid infection?

(Though I will remain skeptical that both of you could be paid shills, can’t trust anything these days)

@Spartacus

Are you aware of any possible health benefits conferred by 200-400mg doses of CBD, daily, used as an anti-inflammatory, with regard to COVID-19 infections?

I take a daily dosage within that range to successfully mitigate inflammation in a permanent, post-operative ligament injury, and I experienced zero respiratory issues to speak of, during my infection. (Did not have the experimental gene therapy injections)

Furthermore, I understand that high doses of CBD are speculated to work in preventing beta-amyloid plaque buildups in the brain.

https://www.goodnewsnetwork.org/cbd-reduces-plaque-improves-cognition-in-early-onset-alzheimers/
https://www.studyfinds.org/cbd-plaque-brain-alzheimers/
https://www.sciencedaily.com/releases/2021/03/210309192548.htm

Can you speak to any possible benefits in mitigating COVID-19 infection damage, by ingesting clinically significant dosages of CBD?

@Spartacus

I have seen some literature about how Nicotine stops other things from bonding to ACE receptors and that it could be a good counter to Covid..
Would you have any comments about that?

What about alcohol? As in recreational alcohol consumption.. What if any effect could you see that having on a Covid infection?


I am curious because I personally went through having Covid just a couple months ago, and I smoke, and I drink more than most people I suppose..
When I caught Covid I did not stop smoking or even smoke less, I took a Bayer aspirin a few times a day (thought it might help against heart troubles, and general soreness), and I bought a couple gallons of Merlot wine to quarantine with..

I smoked as usual and basically drank the wine all day every day in quarantine..
I had a headache for a day and body aches for about 2-3 days, and felt like I didn’t have a lot of energy for a couple days after that..
I also lost my taste and smell for about a week which then gradually came back..

I caught Covid along with 4-5 other coworkers at the same time of exposure..
I had the LEAST severe case out of all of us..
Some younger than me, some older, some in better shape (non-smoker/younger/non-drinker), some in worse shape (fatter)..
I had the least severe case of all..

Could it have had to do with me sipping wine and smoking the whole time? Nicotine and wine antioxidants?
Idk..

Btw we all caught it from someone who had both doses of the Pfizer vax, and he had almost no symptoms..
Ok so maybe he had less symptoms than me, but he was basically an unknowing spreader, who infected almost our entire crew..
I personally know well that vaccinated people can run around spreading Covid and no paper in the world will convince me otherwise..


Am I just super lucky and have good (French/German) genetics, or did I do something right?


Btw gave merits to both of you because I am enjoying your conversation..
A good debate is best to bring out truth, thanks both of you..
(Though I will remain skeptical that both of you could be paid shills, can’t trust anything these days)

@Spartacus

Are you aware of any possible health benefits conferred by 200-400mg doses of CBD, daily, used as an anti-inflammatory?

I take a daily dosage within that range to successfully treat inflammation in a permanent, post-operative ligament injury, with success, and I experienced zero respiratory issues to speak of, during my infection.

Furthermore, I understand that high doses of CBD are speculated to work in preventing beta-amyloid plaque buildups in the brain.

https://www.goodnewsnetwork.org/cbd-reduces-plaque-improves-cognition-in-early-onset-alzheimers/
https://www.studyfinds.org/cbd-plaque-brain-alzheimers/
https://www.sciencedaily.com/releases/2021/03/210309192548.htm

Can you speak to any possible benefits in mitigating COVID-19 infection damage, by ingesting clinically significant dosages of CBD?

You said there was no proof that mind-controlling nanoparticles existed. I showed you that not only do they exist, and not only did James Giordano give presentations about them before an entire class of stunned cadets at West Point, they are described explicitly in publicly-available materials.

Not only that, DARPA, DTRA, and vaccine researchers are intimately connected both to brain-computer interface research, and to GOF research at the Wuhan Institute of Virology.

The degrees of separation here are minuscule. When plotted out on a node graph, they would all cluster together. David Martin and M-CAM showed, beyond a shadow of a doubt, that GOF SARS strains and their features are basically patented products.

That's not a conspiracy theory. That is a RICO case the size of Mount Everest. It is also mass murder and treason.

What do you wanna bet the Human Cattle Ranchers kept the real cure for themselves, and left us all to die?

Micronutrient deficiency is endemic throughout the developed world. Given that 40% of Americans are Vitamin D deficient, some critically so (this gets worse the darker your skin is, with as many as 60% of Hispanics and 80% of African-Americans being Vitamin D deficient), there's no way that one Vitamin D pill a day could hurt. It could only help. Vitamin D helps lower anxiety, too.

https://onlinelibrary.wiley.com/doi/full/10.1002/brb3.1760

Personally, I recommend raising one's levels of Vitamins A, B, C, D, E, and dietary nitrate, and taking NAC, selenium, quercetin, resveratrol, and curcumin, but avoiding hypervitaminosis, which can cause fatigue. The best and most bioavailable sources of vitamins are foodstuffs, not pills.

The best thing for one's blood vessels is to just eat a damn salad instead of hyper-processed, hyper-palatable crap loaded with sugar. Fish for Vitamin D, kale, beets, celery, cabbage, spinach, and kimchi for dietary nitrate, brazil nuts for selenium, garlic for cysteine, and maybe some turmeric-spiced chicken.

You know, a lot of people say that the flu season peaks in the winter time because people are inside and have less vitamin D. Of course, it's only speculation because the links between vitamin supplementation and a healthy immune system are correlative, but perhaps maybe not causal.

A lot of the problem with the Covid studies, including the one you linked, is the small sample size. The control and test group had less than <20 subjects in this study. And then the problem arises about the efficacy of vitamin supplementation on severe Covid infection. Hypothetically, if people supplemented vitamins before infection, their outcome perhaps would be better. Maybe there are studies that might examine vitamin supplementation among a cohort of people that have not been infected yet and follows them throughout a period to determine how many of the supplemented group get a severe Covid infection, versus the control. But for that to happen, you'd need to control for previous infection (and do an antibody titer test) and vaccination status. A bit hard when almost everyone in the first world has either previously been infected or vaxxed.

seriously go die... you speak about control and  test group, and what about those of the mrna ? okay... hop, on the kill list. (FYI the control group have been wiped, and no there wasn't even a short term study on the effect, short or long term of those mrna...).

next...

so mr spartacus...

you speak a lot about oxidative stress in your letter (understand I am a noob and have no intention nor time to skill in this domain) and my question, as question more is important : what about 5g ? I have seen or remember to have seen some stuff about oxydative stress from ionizing, gate transfer, what ever... in short bad. (point 1)

and point 2 : I heard that with all wireless tech introductions, big pandemics ensue, the whole dna/rna shedding warning theory on living organism... to resay it calmly the theory goes that once exposed to wireless non ionizing radiation, livings warn other and shed. do you have an opinion?

and back to the terro above : you fucking muppet : germ theory vs terrain theory... and no it's not all dna, as dna effectively only codes proteins (go Mike, soon FTL to beyond this world :D).

I am not kidding, you are a terrorists, and I hope one day you will be camped and killed.

why?

look you do the same play that you did with HCQ or Ivermectine or even zinc, c, d...

you want for us the highest standard of science, which we are happily producing, but for you, nothing but to trust you.

you see the problem cultist? we are gonna get you, and if it means destroying the fucking entire dod, so be it...

so be it...

get it?

no... until we get you, and we will.

I am not kidding, you are a terrorists, and I hope one day you will be camped and killed.
why?
look you do the same play that you did with HCQ or Ivermectine or even zinc, c, d...
you want for us the highest standard of science, which we are happily producing, but for you, nothing but to trust you.
you see the problem cultist? we are gonna get you, and if it means destroying the fucking entire dod, so be it...
so be it...
get it?
no... until we get you, and we will.

Had you not been so adamant about killing those that dissent, you might've learned that alternate treatments aren't something that I would argue against, only when absent of any true evidence. Treatments of HCQ are largely debunked, and Ivermectin may or may not work. You can find a study from all angles. Zinc, vitamin supplementation, on the other hand, seems promising, but isn't a cure. Basically, you want to be someone that is properly supplemented on vitamins and get Covid rather than be someone with Covid deficient of vitamins. So while you chase debunked treatment options, you miss the ones that actually work - some of which you've listed here.

And who is "we," exactly? Do you mean the other senile dementia patients that were given internet access before their demise?

Wo wo wo, slow down tinker bell. I don't know what triggered you that much but death threats are not cool. How teh fuck you decided that Gyfts is a terrorist? Look what you have done Spartadude, you started the next world war in btt.

they have dow us (declaration of war) and engaged (bio weapon release + denial of treatments + forced injections) what the fuck in the hell more do you want? stop alex jones kool aid plz. it's war. and in war only victory counts, the rest is for the winners to write.

and those aren't "death threat". I want to be clear... it's a war. one side will exterminate the other. end. there is no legal term. only the laws of war.

read his post... denying nutrional deficiencies or imbalances is basic medical practices... basic, level 0. ground floor... you want to heal someone? or chronically customerize it? that's the question. I have my answer... markets need regulations... and if there isn't a more important market than healing, I don't know which one...

as said the war has already been launched... so... what else do you want?

I understand your sentiment but you are barking at the wrong tree. I think Gyfts isn't the terrorist you are looking for. At least that's the impression I got from his/her posts. As I understood, he is leaning more towards right-wing which are mostly against the m-rna vaccines. There are other vaccine worshipers around even in this topic. Why don't you  canalize your hate towards somewhere else? (even then, death threats are not cool)

I am Spartacus. I can answer any questions you may have.
~

...Proof of identity?

Any random weasel on this forum can register an account with "Spartacus" in it.

...Proof of identity?

Any random weasel on this forum can register an account with "Spartacus" in it.

The dude's last post to this thread, which shows a basic command of the scientific principles replete with copious use of the same class of links that the Spartacus docs used, is actually pretty strong evidence that he is not a 'random weasel.'  And even if he is, the information he is bringing is gold.

...Proof of identity?

 I will say this. If he's not Spartacus, this is the most intelligent and well executed LARP I've ever personally witnessed.

 The preponderance of evidence, knowledge, and writing style give me an eerie sense we're not dealing with a "John Titor" situation here.

you are back on ignore, moron.

...Proof of identity?

...Proof of identity?

Any random weasel on this forum can register an account with "Spartacus" in it.

This volume and book series address and reveal the reality that neuroscience and neurotechnology (neuro S/T) have become powerful forces that influence society, and are influenced by various social forces, and incur a host of ethico-legal and social issues. Recent governmental and commercial investments in brain science and neuroengineering reflect growing interest and enthuse advancement(s) in neuro S/T and the information, products, and potential power these disciplines may yield. A dimension of this power is derived from the prospect of using neuro S/T to define - and affect - human nature.

Until rather recently, most efforts toward global relations, as well as national and international security and defense, have focused upon social factors influencing human behaviors, including hostility and patterned violence. Given that these behaviors are devised and articulated by human factors, and humans are most accurately defined as biopsychosocial organisms that are embedded within and responsive to geocultural environments, it is important to address and discern those (neuro)biological factors that are affected by and interact with psychosocial variables to dispose and instigate hostility and violence. Neuro S/T provides techniques and tools that are designed to assess, access, and target these neurological substrates, which could be employed to affect the putative cognitive, emotional, and behavioral bases of human aggression, conflict, and warfare.

This is why Blackrock and Vanguard and the like are buying up rural and suburban properties. They are herding people into cities because the infrastructure for mind control has to be concentrated there. It's too expensive to try and cover all of bumfuck Wyoming with phased-array antennas.

Zillow Group Inc. became the latest company to get enmeshed in internet drama when Sean Gotcher — a real estate agent in Las Vegas — posted a TikTok video that said an unnamed company was pulling off a convoluted scheme to manipulate housing prices in his home market.

Let me translate that for you.

The physicians, the CDC, the public health service comes back and says "no, no, that's not what's going on". I get back on the internet and I say "don't you listen to that,  that's fake, that's false, your government knows what's going on, they can't do anything about it, they can't treat you, they're gonna end up quarantining you." How many people would I need to affect? We modeled it. Somewhere between 12 and 240. What would be the effect? In 41-45 days we would crash the United States public health system.

That's not a "translation", that's speculation, loosely (if at all) related to the quote.

Here is another James Giordano quote for you, since you seem to be very fond of him:


Seems like you got your 12+ here, good job. Using your own standard of evidence "someone mentioned it in a lecture so if we pick the right cherries we can claim that this thing exists and we're living it", that's definitive proof right here that you work for the Chinese government in furthering their bioweapon attack (which of course is also definitely real based on the same standard of evidence).

Or maybe you're full of shit like all conspiratards, albeit more capable to overwhelm your audience with big words and irrelevant links and quotes.

Again, for the people in the back.

Moderna was co-founded by Robert Langer.

...
Let me translate that for you.

They are going to pacify (that is, "cyber-socialize") every human being on the planet completely. They are going to do this by injecting nanoparticles into people that cross the blood-brain barrier, which are activated by external transceivers and precisely stimulate regions in the brain involving mood, reward, anxiety, hostility, et cetera. ...

Oh, so we just skip over the whole "does this tech actually exist" and go straight to insinuating that some people knowing other people definitely means they're conspiring? Does that mean the Pfizer vaccine is safe or is Pfizer founder's niece linked to someone in Wuhan too?

BCI tech is in its infancy even with electrodes physically implanted in one's head. AFAIK the whole nano particle shtick would require a helmet just to read brain activity. OTOH we already have drugs that affect "mood and behavior" so why not just put those in everyone's beer and don't bother with the complicated virus-vax conspiracy.

None of this proves that remote mind control exists, can be covertly delivered via injection to billions of people, and that this actually happened.

I wouldn't think for a second that you really believe that gibberish you're posting, so I'm quite intrigued how far you're going to take this.

The two began with a single volt. Not much happened. The patient’s well-being or “happiness level” was down around two, while his anxiety was up at eight. With another volt, his happiness level crawled up to three, and his anxiety fell to six. That was better but still nothing to write home about. At four volts, on the other hand, the picture was entirely different. The patient now described a feeling of happiness all the way up to the maximum of 10 and a total absence of anxiety.

“It’s like being high on drugs,” he told Synofzik. The neurologist turned up the voltage one more notch for the sake of the experiment, but at five volts the patient said that the feeling was “fantastic but a bit too much.” He had a feeling of ecstasy that was almost out of control, which made his sense of anxiety shoot up to seven.

In brain tissue, the ACE2 mRNA is expressed in the following order of abundance: nucleus accumbens of ventral striatum > posterior hypothalamus > anterior hypothalamus > cortex > hippocampus > cerebellum > spinal cord > medulla oblongata (Harmer et al. 2002).

What I don't get is why we aren't seeing any results for many of these antioxidant trials.

Micronutrient deficiency is endemic throughout the developed world. Given that 40% of Americans are Vitamin D deficient, some critically so (this gets worse the darker your skin is, with as many as 60% of Hispanics and 80% of African-Americans being Vitamin D deficient), there's no way that one Vitamin D pill a day could hurt. It could only help. Vitamin D helps lower anxiety, too.

The evidence I have seen seems to suggest that a deficiency in vitamin D can make COVID worse, rather than extra vitamin D being protective against COVID, but I haven't spent a huge amount of time reading around this topic. Regardless, the majority of Americans are deficient in vitamin D, especially those in more northern states, and should be taking a vitamin D supplement anyway.

88% of the people intubated in New York died.

https://www.webmd.com/lung/news/20200422/most-covid-19-patients-placed-on-ventilators-died-new-york-study-shows#1

During that outbreak, Dr. Cameron Kyle-Sidell vocally expressed concerns that they were using the wrong treatment.

https://z3news.com/w/dr-cameron-kylesidell-treating-wrong-disease-change/

Another study shows that 45% of patients intubated are dying.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781141/

Granted, this is an intervention that is mostly reserved for critical cases that would otherwise have a fatal outcome. I recognize that. However, there has to be some manner of adjunct therapy that can protect the tissues from damage.

What frustrates me is the lack of mainstream media coverage of the deeper complexities of COVID-19's pathology.

A good friend of mine died on one of those ventilators. I hadn't seen him in a few years and I was hoping to meet up with him. This is kind of personal for me, and I may have gotten a little heated up.

Why do I keep seeing studies showing a benefit, then?

The paid shills will correct what the magnets missed
https://ibb.co/JRxztvh

...
Almost all anti-vaxxers deliberately just turn a blind eye to published data and trials. I'm curious as to how you can understand how trials like these are the only way to reach firm conclusions and build an evidence base, but then simultaneously choose to ignore the evidence that the vaccine is reducing symptoms, reducing critical care admissions, and saving lives.

Okay, so you want to put electrodes in the brain. How do you power them if there are no wires? Simple. You use nanoparticles that self-assemble into antennas and circuits capable of harvesting RF and outputting a mild electric current.

How do you titrate the dosage to each person's brain? Simple. You use a source that can steer different beams of different dosages to different people's brains. 5G base stations are phased-array antennas with beamforming and MIMO. Problem solved.

None of this stuff is technologically infeasible. At all.

We see this kind of thing not infrequently in medicine, and even more so in critical care. Drugs or treatments which show promising results in vitro, show promising results in rodent models, maybe even show promising results in healthy volunteers, but when we apply them to critically ill patients, they either don't work or even make things worse.

Take colloids for example. They were going to be the next big thing and replace crystalloids for treating septic shock. They provided a bigger increase in blood pressure than crystalloids, and this increase lasted longer. They stayed in the intravascular space longer, they caused less peripheral and pulmonary edema and fewer third space losses. They allowed us to wean vasopressors more quickly. They made all our numbers and parameters better. And then the studies came out which showed that actually they were pro-inflammatory, they were bad for the kidneys, and they worsened mortality. So we are back with crystalloids except in very specific cases.

Take ventilation for example. When we first ventilated patients, we used large tidal volumes and high respiratory rates to help clear CO₂. We did this to get their PaCO₂ down to a physiological level, which helped to correct the acidosis associated with sepsis and bring their pH back to a normal level, which definitely improved things in the short term, stabilized the patient, reduced the requirement for inotropes and vasopressors, etc. And then the studies likes ARDSnet came out which showed we were causing volutrauma and barotrauma and allowing what we call "permissive hypercapnia" with lower tidal volumes improved mortality.

So then we get a treatment like antioxidants, which logically should work, and which give good looking data in rodents or healthy volunteers, but when applied to a critically ill population, simply don't work.

Emphasis mine. These people would have had a near 100% mortality rate without intubation. I've intubated a lot of people with COVID, and in every single one they were critically hypoxic and, at most, a couple of hours from dying without intervention. It's also worth noting that the article with a mortality rate of 88% was published in April 2020, during the first wave, when we had no specific treatments for this disease. Less than a year later and the mortality rate is now down at 45% precisely because we have evidence showing us which "adjunct therapy", as you put it, is effective. As time goes on, and with other treatments being studied and widespread vaccination, that number will reduce further.

The public don't care. What can they do with knowledge that COVID causes severe DIC or pericarditis? They want to know when they can go on vacation again or go to a concert.

My condolences, sincerely. It's personal for a lot of us.

Mostly low quality evidence. Cohort studies or self selecting studies, low number of patients, confounding factors, etc. One of those studies you linked even found that physical activity was a risk factor for COVID. If you take high quality meta-analyses which only include high quality RTCs, such as the one I linked previously or this one - https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD015017.pub2 - we generally find very sporadic and inconclusive evidence. I'm not saying there definitely isn't something there, but there is no good quality evidence to support it at present.

Almost all anti-vaxxers deliberately just turn a blind eye to published data and trials. I'm curious as to how you can understand how trials like these are the only way to reach firm conclusions and build an evidence base, but then simultaneously choose to ignore the evidence that the vaccine is reducing symptoms, reducing critical care admissions, and saving lives.

Antenna size is directly correlated to wavelength. Minimum antenna size for 5G signal is ~3mm. AFAIK there are some tricks to reduce that slightly, perhaps to 2mm. That's still 4-5 orders of magnitude beyond what is considered nanotechnology. Not gonna fit through the needle either.


Yeah... it is technologically infeasible. The fact that you talk a lot about remote mind control via nanoparticles but provide links to much more limited experiments with electrodes should be a hint that you're not exactly honest with that statement.

Then there is another huge leap between technological feasibility and the ability to do it covertly at scale.

How many nano particles do you need to align to reach 2mm? ...

I had my last post deleted but to remain on topic and within my remit but I will say that it is too late to stop what is about to be rolled out soooooooon but you do have a choice. Participate and live a reasonably comfortable life albeit subject to your benevolent academic overlords and central planners or refuse to participate and life will become difficult. I would personally choose the latter. Life is not too bad as an outcast ;D

The paid shills will correct what the magnets missed
https://ibb.co/JRxztvh

They guy is a dope.  He thinks that nobody can figure out that a variety of antenna designs work well even being less than a wavelength in size.  Else an AM radio would have to be 300 meters long.

Spartacus is reeling them in like a fish. 

We see this kind of thing not infrequently in medicine, and even more so in critical care. Drugs or treatments which show promising results in vitro, show promising results in rodent models, maybe even show promising results in healthy volunteers, but when we apply them to critically ill patients, they either don't work or even make things worse.

To be clear here, I've not gone too deep into the Spartacus Letter. Only about page 3 of the PDF, and the last highlighted term I had is "multinuclear giant cells" that I was off on a tangent learning about - something related/similar to bone marrow or some shit? I dunno, anyway...
...

A potential problem (or solution depending on one's point of view) with making people allergic to spike protein is that you might make them allergic to a placenta when it's needed due to similar proteins being involved with both.

So yeah. There's this film I watched once named "Children of Men". I should probably go watch it again in the post-COVID19 world, come to think of it...

https://www.rottentomatoes.com/m/children_of_men
https://www.imdb.com/title/tt0206634/

They guy is a dope.  He thinks that nobody can figure out that a variety of antenna designs work well even being less than a wavelength in size.  Else an AM radio would have to be 300 meters long.

And "the Matrix 4" is about to be released... Do you think it is a coincidence?

An earlier version of the "vaccine"

Spartacus is reeling them in like a fish.  They put the top guy on the Oilyeo personna which has a ton of groupies who bought the 'I'm a doctor' shtick, then Spars plays Mr. nice-guy and proceeds to hammer his balls flat.  But first a phase of getting them to lay their nads the block and getting the mallet handy.

Currently both are playing a game of 'maybe the corp/gov malfeasance just greater-good subterfuge for the benefit of the herd.'  Nobody thinking person can actually believe that when the situation is looked at in totality, so the trick is to get more people to actually look.  I dare say that the sleeze-balls who commisioned the Oilyeo side are looking frantically about now.  Hopefully Spars has his op-sec wired tight.

suchdope

5th generation mobile network (or any other) is not limited to single wavelenght. Different carrier use differant signal depenting on target audience, longer wavelenght more coverage, higher pulserate need more towers and more susceptible to weather....
60Ghz (5mm) is open usage anyone can use same as 2.4Ghz (Router, bluetooth, wireless headphones....)
T-mobile 600Mhz and 2.5ghz
Sprint 800Mhz, 1.9Ghz, and 2.5Ghz
Verizon 28ghz and 39ghz
Corresponding full, 1/2 or 1/4 wavelenghts (what fraction can be done this days?)
https://www.omnicalculator.com/physics/dipole

Pigeon "freezes" mid air next to 5G tower
https://twitter.com/i/status/1281355107309936640

To be clear here, I've not gone too deep into the Spartacus Letter. Only about page 3 of the PDF, and the last highlighted term I had is "multinuclear giant cells" that I was off on a tangent learning about - something related/similar to bone marrow or some shit? I dunno, anyway...

I understand it starts getting into more conspiracy minded talk later on in the paper, and honestly, my eyes may begin to roll at speculation or theoretical postulations, but in speaking to just the beginnings of the paper - at least - I can say it's been a fascinating, plausible, and accurate read so far, describing how COVID19 affects human physiology.

I'm skeptical AF, and internally am all like "Yeah, right... The Spartacus Letter author is actively interacting with our little corner of the internet, but I've seen stranger things happen, and TBH, this is the best LARP I've seen so far, so I'll pay peripheral attention to it while I do a deep-dive of the letter, cross-referencing the research independent of their footnotes and citations" sorta deal.

Back to metaphorical popcorn.

This is a very fascinating aspect of the whole game-board as it is unfolding.

It is not normal for two cells to join into one bigger cell.  Nor is it a common need most of the time.  Most of the time it would just be a problem and cell membranes are evolved to avoid this happening.

Placental mammals (as opposed to marsupial mammals such as opossum or kangaroo) need to do it in a specialized condition.  Pregnancy.  It is how the placenta begins to form.  It is thought that at some point in the very distant past, a germ cell (egg or sperm) was attacked by a virus which had expressed an interesting protein which provoked this fusion.  Instead of being killed by the virus, the germ cell stole the code...and that's why we humans, and most other mammals, walk the earth today.

This protein?  If you guessed 'spike protein family', congratulations!  That could help explain the seemingly intense interest (and money) dumped into study of the substance within the corp/gov scientific circles.  And the various splicing that appears to have been happening in the various labs working on 'bat coronavirus'.

Wouldn't you know it, but a gene therapy which programmed cells to produce and pump out spike proteins was ready to go just a few days after them chinks made SARS-cov-2 by eating them bats.  It's a miracle!

A potential problem (or solution depending on one's point of view) with making people allergic to spike protein is that you might make them allergic to a placenta when it's needed due to similar proteins being involved with both.  This is quite aside from the ADE risk which is being much discussed lately.  The jargon 'unsafe epitopes' relates to this potential risk.

So yeah. There's this film I watched once named "Children of Men". I should probably go watch it again in the post-COVID19 world, come to think of it...

https://www.rottentomatoes.com/m/children_of_men
https://www.imdb.com/title/tt0206634/

Sure.  Just note that the people who write and act in these things are compensated well in excess of their counterparts at JIDF and suchlike.  But ultimately from the same endless well of money though.

I don't watch movies, TV, Radio, or broadcast media in real-time.  But that's just me.

I don't watch movies, TV, Radio, or broadcast media in real-time.  But that's just me.

Well, you're absolutely right. Something that seems promising in vitro is not always useful in vivo. A drug that works great on a cell culture may never even reach the cells in question when applied to a living body, which is basically a giant maze.

However, that's not what I meant. Look at those links I posted again. Many trials have failed to post any results at all, even over a year after their completion. Not positive, not negative. Nothing. No data. That's so frustrating to see.

Isn't there anything that can be done in terms of surveillance and early treatment before they become critically hypoxic?

I have seen so many instances where people go over the topic of COVID-19 death certificates, hear that a PE, stroke, or myocardial infarction killed someone who was sick with COVID-19, and then angrily grumble something about how hospitals are inflating COVID-19 numbers by designating deaths from infarcts as COVID deaths.

I know they're trying to prevent a panic, but at this stage, more information is better. It has to be.

Lots and lots of people are very scared.

They guy is a dope.  He thinks that nobody can figure out that a variety of antenna designs work well even being less than a wavelength in size.  Else an AM radio would have to be 300 meters long.

Corresponding full, 1/2 or 1/4 wavelenghts (1/4 wavelenghts is over 50 years old, what can be done this days?)

We give out plenty of information, barn door irrefutable information, and still some people deny it.

It is neither experimental nor gene therapy.

A number of possibilities. Could be that they are still writing up the data, but since these trials you linked are generally very small numbers of patients (<100), it shouldn't take them long to analyze. Could be that they failed somewhere along the way with recruitment, or administrating the intervention, or maintaining the blindedness, etc. Could be that their results were negative and so they just gave up and didn't bother to write them up.

If you get as far as the hospital with COVID then you'll get all the treatments we have good evidence for which I outlined above - dexamethasone, remdesivir, tocilizumab, NIV - all with the aim to prevent intubation.

Tell that to your fellow anti-vaxxers. They are the ones perpetuating this nonsense.

We give out plenty of information, barn door irrefutable information, and still some people deny it. People look at the death rates and falsely claim they are being inflated, as you just pointed out. People deny that hospitals are full, when we've literally taken over entire floors to turn them to expanded ICUs. People don't even think COVID is real, despite it being isolated hundreds of thousands of times and killing millions. Explaining the intricacies of COVID pneumonia or multi-organ failure isn't going to change the mind of these people. Indeed, as evidenced by this very thread, if you try to do so you get simply get insulted and told to go die.

Absolutely. And feeding them provable lies about how our single greatest weapon in the fight against COVID is gene therapy or mind control or nanotech or any other nonsense is the root of a lot of that fear.

It is neither experimental nor gene therapy.

ICENI_Spartacus first let me say - thank you for existing. I imagine it must be very hard and tiring especially psychologically to go all in against the powers, against the narrative, and against the everyday normal people that you're trying to save but they don't realise it and attack you (kinda reacting like our own immune systems when they've been cheated and modified by the virus)... collecting information piece by piece like a bee and knowing you will get no reward or recognition even if you succeed in saving us - you're a special person driven by duty and thank God there are people like you. To stay sane and carefully analyse this weird horrific puzzle and to try and make sense out of it. Please don't stop. Even if you are on a wrong path sometimes - don't ever quit or take it as a discouragement as I believe you will eventually get your eureca moment and crack this all and for once. You are important as you have many of the events in your head, and many of the public information since COVID's emergence and in case this public info goes missing online (which is actually happening gradually and with time) - you will still be able to connect the dotts once you gather enough info or logical proof for what's happening. It doesn't matter if you're 1 person or a huge team - this Spartacus letter approach is working and getting to people so you're doing something - very right.

Saying all this I want to ask you the following, if you allow me:

- What's your option on China and their vaccines? Why did China choose to go to the inactivated variant of a vaccine? For me - this is very interesting. US also has been working on inactivated virus vaccine which most definitely won't be used for the masses (perhaps only those high importance will take it). Is China really trying to protect their population from COVID which might have essentially been planned and executed as a bioweapon against them and against the rest of the world (killing China and enslaving the rest of the world). Perhaps they didn't expect China to close down so aggressively and to stop the COVID spread and come up with a vaccine to save themselves. If China were in cahoots with the planners why would they release it on themselves and why would they go the inactivated vaccine route which is less technological (they don't have mRNA technology) and perhaps... actually effective? From my perspective even if China did release the virus themselves to the world they still need to protect themselves with a working vaccine, so both situations require them to come up with a real vaccine... Otherwise why not just use mRNA like everybody else? Geopolitically if this is a war between Anglo-Saxons/NATO against the rest of the world (undeveloped nations who catch up economically and will want their share on global stage) then it makes some sense to look at it at this angle. There is no doubt about the ambitions of some people who want the One World Government but is this truly possible and achievable taking in mind there are also other people (Putin, Maduro, Duterte, Xi Jinping) wanting control of their own countries just as bad. Those people are as megalomaniacal as well - let's not forget that. As much as powerful and rich people align in philosophy - they don't like to share the bone they're holding. And if Macron, Boris Johnson, Biden, Ursula and others of this kind are perceived as tyrants or people of great power nowadays - they've climbed the power ladder rather easily by bending knee in front of their masters and aren't the true masters. So it's expected that they will just follow the agendas and the orders. But this can't be said about Putin, Maduro, Duterte, Xi Jinping etc. Their power ladder was climbed in a totally different way. Do any of us know just how many people has Maduro killed to get on top? Those people have truly earned their power. And to think they will just hand it down to Anglo-Saxons/NATO/ or... Schwab. Just because they have the same hunger to oppress people... well they already do this. If anything - democracies are scary because they allow free speech. And Venezuela, Russia, China aren't quite the democracies and never actually were even close to that. So what is your geopolitical stance and your China vaccine stance? What happens in the body when Sinovac or Sinopharm is used? What does the inactivated COVID do? I think we can pretty much disregard vaccine side effects as a proof of bad intentions as if you think logically... if their intention is to control populations by the vaccine, then the COVID itself will be the population reduction mechanism and the vaccine side effects are just... vaccine side effects (also why would they scare population by side effects like it's happening now... they want the population to actually take it... I think they just screwed up "Windows BSOD" style...) because all vaccines have them - side effects, especially the non-tested ones, and the rushed ones to the market. Also what is your proposed treatment/prevention protocol for coagulopathy?

Neutrophils are key players in the pathophysiological process underlying inflammatory conditions not only by release of tissue-damaging cytotoxic enzymes, reactive oxygen species (ROS) but also by secretion of important immunomodulatory chemokines and cytokines. Here, we report the effects of the novel agent APPA, undergoing formal clinical development for treatment of osteoarthritis, and its constituent components, apocynin (AP) and paeonol (PA) on a number of neutrophil functions, including effects on TNFα- expression and signalling. Neutrophils were treated with APPA (10-1000 µg/mL) prior to the measurement of cell functions, including ROS production, chemotaxis, apoptosis and surface receptor expression. Expression levels of several key genes and proteins were measured after incubation with APPA and the chromatin re-modelling agent, R848. APPA did not significantly affect phagocytosis, bacterial killing or expression of surface receptors, while chemotactic migration was affected only at the highest concentrations. However, APPA down-regulated neutrophil degranulation and ROS levels, and decreased the formation of neutrophil extracellular traps. APPA also decreased cytokine-stimulated gene expression, inhibiting both TNFα- and GM-CSF-induced cell signalling. APPA was as effective as infliximab in down-regulating chemokine and IL-6 expression following incubation with R848. Whilst APPA does not interfere with neutrophil host defence against infections, it does inhibit neutrophil degranulation, and cytokine-driven signalling pathways (e.g. autocrine signalling and NF-κB activation), processes that are associated with inflammation. These observations may explain the mechanisms by which APPA exerts anti-inflammatory effects and suggests a potential therapeutic role in inflammatory diseases in which neutrophils and TNFα signalling are important in pathology, such as rheumatoid arthritis.

So I was hoping that this thread would show up on search engines searching “Spartacus letter”, but it does not..

Google.. Sigh..
Google has one real hit leading to a fact checker calling it false.. All other results are not applicable..

Bing and duck pull up many articles about it, but no links to this thread..

How do we fix that?
Cross post links to this thread to other forums and such?

I am no SEO expert..
Y’all that know what your doing should make this shit trend/go “viral”.. heh
Post it on Twitter and Reddit or whatever

So I was hoping that this thread would show up on search engines searching “Spartacus letter”, but it does not..

By all hells watch this : Dr. Carrie Madej joined Stew Peters today and appeared obviously shook by what she had seen after examining Moderna and J&J "vaccine" vials.
4:30 https://www.brighteon.com/aa151644-a720-4842-8116-c016ffc64c58

omfg... self assembling structures... so for the BCI it would work to reach the 2mm length... at 60ghz what's the minimal length of the antenna? and would it be possible without even using self replication/assembling antenna to just use the own body as an antenna? I mean to use bones or structures in the corpse as length amplifier to achieve reception of commands?

now pics...

ommmmggggg..... alien covenant / life ///// end of time / give me my crysis suit NOOOOOOOOOOOOOOOOOOOWWWWWWWWWWWW

edit that's what she fucking saw at 400x zoom (because muppets say magnification and fuck muppets).

https://i.ibb.co/VmMcY2p/1.png

self assembling antenna

and now... omg omg omg omg omg omg omg omg omg... save us ! death come (aka salvation with death)

https://i.ibb.co/cCnN8s2/2.png

it's beyond words...

I have watched the video. She's coming off quite authentic, until the point where she said that "nothing has been added... no human tissue... ", she started to support her creative (right) hemisphere of the brain by looking to the left very often, particularly when which she talks detailed about what she examined was happening.
As a long time poker player, i can tell you that she's almost certainly making a lot of things up. If you don't believe me, i don't have the time to convince you, sry.

Now, the facts: Some proteins are used, so they would certainly de-naturate under the warm light of the microscope. Just split an egg over a pot of boiling water. No videos of the "tentacles" moving were shown, only stills. The Dr. lady is also an Osteopath, google that.
She already brought out some other fake finding, which was debunked already.

Just my three cents

If there are so many patients, why are the sample sizes so small? If our hospitals are flooded with dying people, as you say, then why can't they enroll more than a handful at a time? Surely, there should be a surfeit of people who could participate in these trials.

Antivirals pretty much don't work unless they're taken as post-exposure or pre-exposure prophylaxis.

The Kaplan–Meier estimates of mortality were 6.7% with remdesivir and 11.9% with placebo by day 15 and 11.4% with remdesivir and 15.2% with placebo by day 29.

These patients need early, proactive interventions to prevent them from progressing to sepsis.

It is difficult to warn people about a virus and its properties when the fundamental knowledge is so lacking. I do indeed blame the government and the rapidly declining quality of public education for that. People are wearing scientific ignorance as a badge of pride, because science has become so politicized. It shouldn't be. Knowledge is power, and science is merely a means of obtaining knowledge.

The government guidelines should be for people to stay active, stay healthy, diet correctly, and lower their BMI if they're overweight or obese. This would, in the long run, save many lives, because the evidence for COVID-19 causing greater mortality in people with a higher body-mass index (likely due to pre-existing endothelial dysfunction) is overwhelming.

Given that the IFR of COVID-19 is relatively low in absolute terms, not even near to approaching the lethality of something like Smallpox (which people lived with day in, day out, without any economic disruptions whatsoever, despite the gruesome toll in lives it took every year), the lockdowns and the strange behavior of our governments makes no sense unless there is an ulterior motive.

Furthermore, it is entirely possible for mRNA to be integrated into one's genome by endogenous reverse transcription.

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

Speaking to more esoteric meta issues, can you speculate on the possible negative consequences to going through the infection process, surviving, acquiring the natural antibodies, and appearing to make a full recovery such that you can resume life?

@o_e_l_e_o

Not to be offensive, but at this point I'd rather trust ICENI_Spartacus on everything medical although I'm sure he's no doctor and you're actually a real doctor. And do you know why? Because this anonymous man/woman/whatever is actually trying to connect the dots like... logically. For both the virus and the international situation. Taking all conspiracy theories away, ICENI_Spartacus is reading, anaylsing and thinking - exactly what should be done. And what are you doing dear doctors? Listening for orders from "above" - your boss, your tv, your politican. You're not doing the analysing, you're not doing the thinking. You MAY be doing the reading, but only from the sources that your boss, your tv or your politican gives you. And this is truly sad. Being outsmarted by a nobody after wasting so many years and money in the med school? I have one advice for you - stop being static, sleepy and obedient. Start using your prefrontal cortex as a real human  being. Stop being cocky "I'm a doctor so I know" - no you don't. Anybody (or a nobody) can read medicine books, literature, spend the time you spent and gain the information you've gained. Not everybody are doing it, but some are. In the age of internet and information and cheap coffee you only need curiousity and free time. The difference? Those people who aquire ANY knowledge by NECESSITY (like ICENI_Spartacus) are the people who are most likely to use it properly. Because there is zero influence from a boss above etc. You (and your colleagues) may be fired from your hospital if you start thinking the "wrong" way and that's why you've had your railways set up and your cozy place promised - to get your salary and do what they tell you to do and think. This situation doesn't exist for the others. So again... with all due respect - don't even think you may have any authority here because you're a doctor or work in a hospital. Your authority will come after we read some thoughts, questions, hurdles, riddles from your posts... show that you're a THINKING man. Now just a man who thinks that if he doesn't know something then others who told him know. Doctors (most) nowadays have become simply just a messengers to the agenda. And even if this is not true, even if COVID is not a wild conspiracy you've already shown that you can be easily put on railways and made to follow agendas without you daring asking questions. Viva free people, free world and free knowledge.

@o_e_l_e_o

Not to be offensive, but at this point I'd rather trust ICENI_Spartacus on everything medical although I'm sure he's no doctor and you're actually a real doctor.

Not to be offensive but your an idiot.

@o_e_l_e_o

Not to be offensive, but at this point I'd rather trust ICENI_Spartacus on everything medical although I'm sure he's no doctor and you're actually a real doctor. And do you know why? Because this anonymous man/woman/whatever is actually trying to connect the dots like... logically.

You and @Hueristic are cracking me up :) Never thought people could be so lost/dumb/sad to not actually pay attention to what's written, but instead to HOW. Wow, aren't you some linguistic expert... You're hopeless/angry/rude and probably have personality issues and overcompensate. The one wishes me bad things, the other insults me using bad language. And we don't even know each other :) You must be so damanged. I am here to make a discussion with @ICENI_Spartacus and not with you :)

Not to be offensive but your an idiot.

So when you have a broken leg or appendicitis you get a random "man/woman/whatever" to fix you up instead of a real doctor?

This must be the stupidest thing I've read on the intertubes today. Well, at least in the last hour. I hope you're just trolling.

Such fun long term symptoms to choose from include fatigue, headaches, memory impairment, attention disorders, chest pain, breathlessness, hearing loss, joint pains, palpitations, depression, sleep apnea, psychiatric disorders, digestive problems, the list goes on.

In your professional opinion, does subjecting yourself to the experimental gene therapy, prevent you from contracting these long term symptoms?

IOW, do the risks of being injected with the experimental gene therapy, outweigh the risks being mitigated for the aforementioned long term symptoms? Does the experimental gene therapy show any efficacy, at all, to mitigate these long term effects?

Specifically, the risk of rogue mRNA-generated spike proteins shredding your vascular cells, as a result of being injected.

As a long time poker player, i can tell you that she's almost certainly making a lot of things up. If you don't believe me, i don't have the time to convince you, sry.

Does it probably help enough for the risk to outweigh the reward?
Maybe in the short term.. Probably in the short term.. Yes..
It does seem these experimental gene therapies probably do help protect from these symptoms, for about 4-6 months..

Then you have to have more experimental gene therapy for it to keep working.. “boosters”
2 to start and then another booster every 6 months FOR THE REST OF YOUR LIFE..

Now..
Is the risk of one shot better than the risk of Covid?
2 shots?
Ok maybe..
3 shots?
4 shots?
10 shots?
21 shots in the next 10 years?


So what next?
What if you get boosters twice a year for the next 5 years, and then stop?
Are ya fucked?
Who knows..
They do not know..

I can't speak for other centers, but in my center pretty much everyone is in a trial. Can't have a patient in two trials at once since your results would be meaningless. Far better to enroll people in to a big trial of a substance which had encouraging results in small trials than a substance which had negative results in small trials.

Earlier treatment is obviously better, but there is still evidence for remdesivir once the patient is admitted to hospital, otherwise we wouldn't be using it.

Like vaccination.

Pretty much every government does tell people to do that, and it would save many lives from cancer, heart disease, diabetes, stroke, etc., not just COVID. Figure out a way to convince people to do it and collect your Nobel Prize.

Because smallpox had existed for centuries and many people were already immune due to either variolation or childhood vaccines. COVID came out of nowhere and there was no pre-existing immunity. An unjust comparison.

I'll skip over all your mind control nonsense to address this. You've just linked a study which says "This novel feature of SARS-CoV-2 infection may explain why patients can continue to produce viral RNA after recovery and suggests a new aspect of RNA virus replication." Once again, you are making a great argument for getting vaccinated and avoiding all these potential complications of COVID infections.

Rapidly accumulating evidence demonstrates that new genes play diverse functional roles and serve as a major driver of phenotypic evolution1. One important mechanism to create these lineage- or species-specific genes is RNA-based duplication or retroposition1, in which an mRNA template is reverse transcribed by retrotransposons and subsequently reinserted into the genome as a functional retrocopy or retrogene2. The identification of retrogenes is straightforward given the hallmark of intron loss relative to the parental copies. Moreover, because of the loss of most of the preexisting regulatory sequences, retrogenes are predicted to be subject to neofunctionalization, i.e., to play a different function compared to their parental genes3. Thus, retrogenes have been an attractive research target for decades. For example, one of the first reported new genes, jingwei in Drosophila, is a retrogene4. In plants, genome-wide surveys performed by others and ourselves have identified numerous retrogenes in Arabidopsis (Arabidopsis thaliana), rice and so on5,6,7. Although the majority of these retrogenes are functionally uncharacterized, Sun is known to underlie morphological variation of the tomato fruit8, while CYP98A8 and CYP98A9 are involved in pollen development in Arabidopsis9.

Although, the LINE-1 enzymatic machinery preferentially reverse transcribes its own RNA (Esnault et al., 2000; Wei et al., 2001; Kulpa and Moran, 2006), the presence of intronless pseudogenes scattered throughout mammalian genomes points out that mRNAs transcribed from protein-coding genes are also substrates for reverse transcription by the endogenous RT (Pink et al., 2011). This suggests that the RT-depending mechanism, in addition to targeting miRNAs, can also target several more RNA classes, coding and non-coding, small- and long-RNAs, though with a possible preferential bias for those associated with, or derived from, retroelement sequences.

Take your pick: https://www.nature.com/articles/s41598-021-95565-8

Such fun long term symptoms to choose from include fatigue, headaches, memory impairment, attention disorders, chest pain, breathlessness, hearing loss, joint pains, palpitations, depression, sleep apnea, psychiatric disorders, digestive problems, the list goes on.

Thomas Renz claims 45,000 dead from the vaccines:

https://rightsfreedoms.wordpress.com/2021/07/22/vaers-whistleblower-45000-dead-from-covid-19-vaccines-within-3-days-of-vaccination-sparks-lawsuit-against-federal-government/

A report to VAERS generally does not prove that the identified vaccine(s) caused the adverse event described. It only confirms that the reported event occurred sometime after vaccine was given. No proof that the event was caused by the vaccine is required in order for VAERS to accept the report. VAERS accepts all reports without judging whether the event was caused by the vaccine.

There will be NO going back to the "old normal". The acolytes of the new global order are too well organised and too powerful for any "man" to undo their plans. TPTB will seal the deal once your FIAT money is removed from underneath your mattress, jam jar and pockets. When cash is gone kiss goodbye to any level of individual control you have over your lives and thank all the plebs on this forum and zombie fooks with their latest pay app or microchip who are heralding it into existence through the crypto "popular culture" and convenience over personal privacy choices .The plebs will literally beg for their enslavement while those who resist will be trampled over and insulted and slandered as terrorists,criminals etc as per protocol by media whores who are bought and paid for.Y'all are being played like a fookin banjo and when you are a digit within a strong city tagged like cattle on a meshed sensor smart farm you will have your digits frozen on yer block and chain when you refuse to comply with the ordinances of technocratic tyrants. And yeah once the block and chain is embedded into mainstream existence within each citadel you can wave goodbye to independent competing currencies which will likely be outlawed,forced into central bank regulatory compliance or simply regulated out of existence.

True story bro ;)

@ICENI_Spartacus, can you answer us this?

"1. What do you think of al-hijama method immediately after taking the vaccine or just keeping a ginant neodymium magnet on your arm and then cutting the skin to release the vaccine? There are videos of people doing that - are they successfully extracting the vaccine this way?"

Thank you... I'm sure there are others who wonder the same... Thank you for your work!

~ you two stop dicking around ~

What's the point? Anyone who knows about "Spartacus letter" probably knows where to find it, and also the fact check article that you mention actually has a link to the letter. What you really want is SEO for "covid conspiracy" or "vaccine mind control" or whatever it is you're trying to do with this letter.

Who cares??

They can't take my crypto away.

Sure they can remove FIAT but how about crypto?

How teh fuck you came to this conclusion that crypto is slavery? Crypto is freedom you nocoiner piece of shit.

When this is over, and it will be over, bitcoiners will be the new rulers of this world.

Not to be offensive, but at this point I'd rather trust ICENI_Spartacus on everything medical although I'm sure he's no doctor and you're actually a real doctor. And do you know why? Because this anonymous man/woman/whatever is actually trying to connect the dots like... logically.

You're not doing the analysing, you're not doing the thinking.

So when you have a broken leg or appendicitis you get a random "man/woman/whatever" to fix you up instead of a real doctor?

Does the experimental gene therapy show any efficacy, at all, to mitigate these long term effects?

Who cares??

They can't take my crypto away. Sure they can remove FIAT but how about crypto? Crypto is above any government or special agency for that matter. How teh fuck you came to this conclusion that crypto is slavery? Crypto is freedom you nocoiner piece of shit.

When this is over, and it will be over, bitcoiners will be the new rulers of this world.

edit: sorry that was offensive a lil bit I lost myself.

Why not the following 6 antioxidants? Ashwagandha, PQQ Pyrroloquinoline quinine, Coenzyme Q10 (ubiquinone), α-Lipoic Acid, Ginseng, Resveratrol.

...

Many of them are believers of Antoine Béchamp who think that germ theory is actually wrong and viruses do not cause disease.
  <snipped, but well worth reading.>

 'confusion, inefficiency, and demoralization.'

Lol. You trust them because they agree with your preconceived opinions. If someone else made a long post with lots of references saying that vaccines worked (you know, like the thousands of trials and studies which do exactly that), you would ignore them.

Part of the issue with thinking that watching YouTube videos is somehow comparable to a medical degree and decades of first hand experience and ongoing education (apart from, you know, being an insane opinion), is that you can't even appreciate the disconnect between the two positions. Let's address the topic of reading and analyzing, since that is the one you brought up.

There is more to reading literature than just firing off lists of papers which you have hastily Googled which you think support your cause. You need to learn how to critically analyze research, weed out low quality case series or retrospective cohort reviews, pick out clear and hidden biases, assess the methodology, look for flaws in study designs and protocols, search for conflicts of interest, find any reporting errors, data errors, analysis errors, statistical errors, assess whether the data support the conclusions, the list goes on. Not only do anti-vaxxers not know how to do this, they don't even realize it is a process which should be done or even exists, which explains why they think a Bitchute video or some far right conspiracy blog is somehow "good evidence". It helps to explains why Spartacus is confused about why good quality trials show no evidence for the treatments they think should work based on poor quality trials. It explains why they link papers which are irrelevant to what they are talking about, mistakenly thinking they support their opinions, and why they links papers which make a very good case for vaccination. And it explains why anti-vaxxers are so impressed by a list of references that you have not read which do not support the points you think they support.

I have never claimed to be an absolute authority on anything, but I know how to read and analyze data and reach logical conclusions based on those data.

I know when we were paying for our house to be built, rather than go to a certified architect and then take the plans to a registered construction company with decades of experience, we instead hired some guy who had never designed or built anything in his life but had watched a lot of vlogs. It was far cheaper! The fact that I am now living in a pile of rubble is irrelevant.

We know that if you have severe COVID then you are more likely to suffer from one or more long term sequelae. We also know that if you get vaccinated, then your risk of catching COVID is significantly reduced, and if you do still catch it, the severity of your disease is in general significantly reduced.

This study, using a virus-free mouse model, explores the pathogenic roles of certain antibodies specific to the spike proteins of highly pathogenic coronaviruses such as the COVID-19 and the SARS-CoV viruses. Our data showed that these pathogenic antibodies, through a mechanism of Antibody Dependent Auto-Attack (ADAA), target and bind to host vulnerable cells or tissues such as damaged lung epithelium cells, initiate a self-attack immune response, and lead to serious conditions including ARDS, cytokine release, and death. Moreover, the pathogenic antibodies also induced inflammation and hemorrhage of the kidneys, brain, and heart. Furthermore, the pathogenic antibodies can bind to unmatured fetal tissues and cause abortions, postpartum labors, still births, and neonatal deaths of pregnant mice. Novel clinical interventions, through disrupting the host-binding of these pathogenic antibodies, can be developed to fight the COVID-19 pandemic. In addition, the new concept of ADAA explored by this study may be applicable to other infectious diseases, such as the highly pathogenic influenza infections. It should be noted that the majority of anti-spike antibodies are non-pathogenic, as only 2 of 7 monoclonal antibodies tested showed significant pathogenic effects.

@ICENI_Spartacus, can you answer us this?

"1. What do you think of al-hijama method immediately after taking the vaccine or just keeping a ginant neodymium magnet on your arm and then cutting the skin to release the vaccine? There are videos of people doing that - are they successfully extracting the vaccine this way?"

Thank you... I'm sure there are others who wonder the same... Thank you for your work!

OK, I’m literaly asking for a friend.

@Spartacus

what the cia do? rage in raping more white kids with fbi agents under the watchful eyes of the doj? (excluding the special rape clubs of the dod, as they are exclusive to the traitors in green)?

Meta: This is a quality of Poker players, that made me recognize I don't have the mental fortitude or stamina to participate in the game, with anything approaching a description of fun.

I suffer from depression/anxiety disorders (treated), and the discipline required to "read the table" is too much for my simple trog brain, to deal with that level of theatrics.

I get so lost in trying to read the table, that I lose track of the cards in my hand, sorta thing, and fail to see the forest through the trees.

The human brain is such a strange organ.

To reach high temporal and spatial resolution, N3 will focus on two approaches: noninvasive (Technical Area 1 –TA1) and “minutely” invasive (Technical Area 2 – TA2) neural interfaces. Noninvasive interfaces will include the development of sensors and stimulators that do not breach the skin and will achieve neural ensemble resolution (<1mm3). Minutely invasive approaches will permit nonsurgical delivery of a nanotransducer: this could include a self- assembly approach, viral vectors, molecular, chemical and/or biomolecular technology delivered to neurons of interest to reach single neuron resolution (<50μm3). In this application, the developed technology will serve as an interface between targeted neurons and the sensor/stimulator. They should be sufficiently small to not cause tissue damage or impede the natural neuronal circuit. The sensors and stimulators developed under the minutely invasive approach will be external to the skull and will interact with the nanotransducers to enable high resolution neural recording and stimulation.
Both noninvasive and minutely invasive approaches will be required to overcome issues with signal scattering, attenuation, and signal-to-noise ratio typically seen with state of the art noninvasive neural interfaces. Systems that are larger or requiring a highly controlled environment – such as magnetoencephalography (MEG), or magnetic resonance imaging (MRI) – and proposals describing incremental improvements upon current technologies, such as electroencephalography (EEG), may not be considered responsive to this BAA and may not be evaluated.
Final N3 deliverables will include a complete integrated bidirectional brain-machine interface system. Non-invasive approaches will include sensor (read) and stimulator (write) subcomponents integrated into a device (or devices) external to the body (Figure 1B). Minutely invasive approaches will develop the nanotransducers for use inside the brain to facilitate read out and write in (Figure 1A). Minutely invasive approaches will also develop the external subcomponents and integrated devices that interact with the internal nanotransducers. N3 developed technologies may move beyond the traditional voltage recordings associated with action potentials, and include different types of signals, such as light, magnetic/electric fields, radiofrequency, and neurotransmitter/ion concentrations. These atypical signals may require the development of new algorithms to enable accurate decoding and encoding of neural activity. To that end, the N3 program will include a computational and processing unit that must provide task- relevant decoded neural signals for control in a DoD-relevant application. It must also provide the capability to encode signals from a DoD-relevant application and deliver sensory feedback to the brain. The processing unit must decode/encode in real time with minimal system latency (Figure 1C). A block diagram of the expected final prototype is shown in Figure 2.
To prove the capabilities of the N3 system, four major demonstrations will show progress from a benchtop proof-of-concept, to validation in animal models, to a final demonstration of a DoD- relevant application in human subjects. In order to transition the developed technology to clinical readiness, N3 performers will actively collaborate with the Food and Drug Administration (FDA) throughout the program.
ABC
Figure 1. Notional N3 prototype. 1A - Nanotransducers supporting read and write functions (for TA2 devices only). 1B right - Notional concept of at least two subcomponents integrated into one device. 1B left – notional diagram of multiple devices used to achieve multi-focal interaction with the brain. 1C - Processing unit for decoding and encoding computation between the N3 system and relevant DoD application.
   (minutely invasive devices only)
 Internal
Figure 2. Block diagram of N3 technology
External
6

HR001118S0029, Next-Generation Non-Surgical Neurotechnology
1.2. TECHNICAL AREAS
The N3 program will provide up to four years of funding to deliver a nonsurgical neural interface system and is divided into three sequential Phases: Phase I (base effort)– 12 months, Phase II (option) – 18 months, and Phase III (option) – 18 months. N3 anticipates that each proposal will involve multiple integrated teams (from the same or different institutions) collectively developing the technological approaches for read out and write in. Teams must structure proposals as a single, unified effort with a system integrator that address all the program goals of the specified Technical Area (TA). Proposals that do not address all of the technical objectives may be considered non-responsive. Proposals must address a complete bidirectional neural interface system based on at least one of the following TAs:
Technical Area 1. Noninvasive neural interface
Technical Area 2. Minutely invasive neural interface
System Integration
Due to the complexity and performance objectives of the N3 system, proposals must identify a lead integrator with a proven track record of managing and integrating disparate technologies. Starting as early as Phase I, system integration should be a consideration throughout the program.
Security Measures
Proposers must use approaches that ensure confidentiality, integrity, and availability (also known as the CIA triad) to prevent spoofing, tampering, or denial of service. It will be necessary to adequately secure the connection between the integrated device, the processing unit, and the system user’s brain. Proposers must incorporate inherently safe techniques into any wireless and electronic portions of their system, and proposals must describe the specific protocols and techniques to be used.
Ethical, Legal, and Societal Implications (ELSI)
DARPA maintains its commitment to ensuring that efforts funded under this BAA adhere to ethical and legal regulations currently in place for federally and DoD-funded research. Program developments will be discussed with a panel of expert external advisors with expertise in bioethical issues that may emerge as a consequence of advances in neurotechnology. Proposers to this BAA must address potential ethical, legal, and societal implications of their proposed technology.

They are asking researchers to come up with a nanoparticle transducer that has single-neuron resolution, which can be ingested or injected into someone (that is, introduced into the body non-surgically), bypass the blood-brain barrier, self-assemble in the brain, and facilitate two-way communication with neurons via an external encoder/decoder system.

Which part of it refers to a 24-52 GHz antenna capable of power delivery over ~500ft distances? You know, the 5g nonsense that you claimed is simple?

And yes, it's a grant proposal, meaning as recently as 2018 they didn't have anything even with a helmet. So I guess thanks for debunking yourself.

@Spartacus

A couple of my pilot friends, received word that their airlines are mandating all staff be vaccinated, irrespective of natural immunity status - that both pilots have, as they have both contracted and recovered from COVID19.

They are currently having their union reps going to bat for them, and are individually looking into religious exemptions, but one of them did pose this question, that I wanted to pass along, here.

Would greatly appreciate any helpful anecdotes or insight you may be willing to share.

Thank you.

"Does anyone have any reading about how covid vaccines affect people who already have antibodies from their bodies beating the virus?"

Wrong again.

https://www.youtube.com/watch?v=cL3e8tC8TwE

https://www.youtube.com/watch?v=7PkV25ZzwTo

The tech is already here and the motive is clear.

Someone already successfully argued for their natural immunity in court.

so, tomorrow i go for a brain MRI. had my 2 dose Pfizer vaccine 5 months ago.

so what say the gang as to what happens to me.. do all the little 5g nanobot mind control devices get extra power? will they suck all the power out of the hospital electrical system through the MRI machine and cause mass mayhem? will they form weird 5 dimensional antenna shapes in my head? will they all get sucked out and stick to the MRI machine? will i suddenly start making useful posts?

gimme your best guess and if i survive i will let yall know what went down.

Pedogate is real, and it's far worse than people think.

This is a node graph of Jeffrey Epstein's connections:

https://graphcommons.com/graphs/0a79deca-46a2-48e9-9d90-326b20aa6e9e

These are the people Jeffrey Epstein did business with:

https://www.mintpressnews.com/cia-israel-mossad-jeffrey-epstein-orwellian-nightmare/261692/

https://www.mintpressnews.com/mega-group-maxwells-mossad-spy-story-jeffrey-epstein-scandal/261172/

And this is what was going on in Belgium during the Dutroux scandal:

https://wikileaks.org/wiki/Belgium:_Dutroux_dossier_summary,_1235_pages,_2005

The Human Cattle Ranchers use pedophilia blackmail to haze prospective members, seal contracts, et cetera. Essentially, the highest levels of government, espionage, and finance are captured by a pervasive and highly pernicious form of organized criminal syndicate.

These people are engaged in a massive, global power grab partly because they fear the consequences of exposure to the general public, which would be dire for them indeed.

Allegations that Pfizer are conducting experiments on six-month-old orphans to test their Covid-19 vaccine have been made by whistleblowers in Poland leading to a group of lawyers, medical professionals and activists demanding members of the Polish parliament and Senate organise an urgent conference on Saturday 2nd October.

Turn the auto-generated subtitles on and watch:

https://www.youtube.com/watch?v=Xopz626cy_M

^

A Turkish professor says, "...We vaccinated some children with biontech by mistake and the results were very satisfying. Even 1 month old, 6 months old babies showed very good results and we will publish the results on a very famous magazine. Even the little kids when you give them a high dose, they showed no problems..."

A professor publicly admits that he gave little kids high dose mrna vaccines by mistake and he is proud of it. He even says he will send his mistake-study to a very reputable magazine to be published.

---

Another disgusting news coming from Poland:

Pfizer stand accused of experimenting on orphan babies to test their Covid-19 vaccine (https://theexpose.uk/2021/10/01/breaking-pfizer-stand-accused-of-experimenting-on-orphan-babies-to-test-their-covid-19-vaccine/)

---

W T F?

(Sabbatean-)Frank(ist)ly, that's pretty mild behavior by Turkish ethical standards it seems to me.  Maybe or maybe not a legacy/function of the Donmeh 'Young Turks' stuff.  It would not surprise me about the Polish/Pfizer stuff either.  Nor would it surprise me if most of the vaxxers thought that both things are perfectly A-OK because it is 'for the greater good' and all, and the so-called 'anti-vaxxers' are to backward/simple/Christian/whatever to be able to see the 'nuances' of their superior logic and 'stronger' leadership.

Uhm... another round of funding. Showing that the tech was still not "here" even in 2021.

And still talking about a "headset". Not even close to what you're insinuating.

A headset just gives you a high degree of spatial resolution. If there is a way to RF-sensitize neurons with self-assembling nanoparticles, then you could still very likely stimulate large clusters of neurons with lower precision from afar using future, high-precision versions of beamforming/MIMO.

A headset just gives you a high degree of spatial resolution. If there is a way to RF-sensitize neurons with self-assembling nanoparticles, then you could still very likely stimulate large clusters of neurons with lower precision from afar using future, high-precision versions of beamforming/MIMO.

https://www.youtube.com/watch?v=l4OwU1p8_tE

Beamforming and MIMO give the system two attributes necessary for mind control. Selectivity (you can send a specific beam of coherent RF into just one person's head), and dose titration (you can select the intensity).

I never considered myself particularly against vaccines or 5G in general. I always found the backlash against them inorganic. In fact, it most likely was.

The conspirators behind this, wealthy and connected as they are, have pushed anti-vaccine and 5G conspiracy theories intentionally over the course of the past decade in order to poison the well and make criticism of their plans appear worthy of ridicule. No one could have guessed what the real plan was, or that the final implementation involved a combination of tainted vaccines and GSM wireless infrastructure to create a mass societal pacification field and lock people into unending serfdom.

That's not to say concerns about vaccines and 5G are invalid. Oh, no, hardly. Vaccines contain metal adjuvants and preservatives that can cause long-term neurotoxic effects, and the health effects of 50 GHz wireless radiation on the human body are largely unknown, but Swiss doctors and biologists (some of the best in the world) have called for a temporary halt to GSM network infrastructure upgrades in Switzerland. They would know.

But still, this is not about vaccines or 5G as health hazards per se (although vaccinating against SARS-like viruses has its own, separate hazards). This is about the surreptitious injection of brain-computer interface components into unsuspecting people, and then their manipulation with GSM infrastructure, neither of which have anything to do with preventing viral infections or facilitating free and voluntary communication.

I don't think it has anything to do with race. Sure, Turkey is not the most moral country in the world but which country is nowadays? Only Crotia's president made sense lately.

President of Croatia: We will not be vaccinated anymore  (https://www.youtube.com/watch?v=cXTGgup_Yto)

All the others are just globalist muppets.

Now you're just posting buzzwords. MIMO helps with bandwidth, it doesn't defy the laws of physics, doesn't make the inverse square law disappear, doesn't make antennas smaller (probably the opposite). There is a reason why those experiments are done with helmets/headsets, and use light, sound etc, not to mention the entirely different purpose (voluntary use e.g. for disabled individuals to regain certain functions).  Adding multiple layers of speculation and extrapolation on top of that just further proves that you don't really have anything to support your preconceived assumptions about vaccines and mind control.

By invoking the inverse-sequare law, you are doing a couple things that are incorrect simultaneously. First, you are assuming a false equivalence between a beamforming antenna that sends concentrated, coherent beams of RF at a single target with an ordinary antenna that radiates energy isotropically. Second, you are also assuming that the power density of the system must be high in order to bring about any physiological effects. This is not necessarily true. It may be the case that self-assembling nanotransducers surreptitiously placed in the brain may only need to harvest nanowatts to induce profound changes in neuronal activity. The amount of energy that actually reaches them could be very small, and yet still achieve the desired effect.

I don't think it has anything to do with race. Sure, Turkey is not the most moral country in the world but which country is nowadays? Only Crotia's president made sense lately.

President of Croatia: We will not be vaccinated anymore  (https://www.youtube.com/watch?v=cXTGgup_Yto)

All the others are just globalist muppets.