Stuff & Stuff
Infra-Universal Journal of Sci-Tech News-Olds &
Updated @ 29 September 2021 [
SARS-CoV-2: Isn’t It Time Someone Did this?
Idaho doctor reports “20 times increase” in cancer
among those “vaccinated” for covid
Dr. Ryan Cole, a board-certified pathologist and diagnostics
lab owner and operator based out of Idaho, has released shocking
new information about how Wuhan coronavirus (Covid-19) “vaccines”
are causing a massive “uptick” in autoimmune diseases and cancer.
In a video produced by the Idaho state government’s “Capitol
Clarity” project, Cole revealed how he is now seeing a 2,000
percent chronic illness increase in folks who took Donald “father
of the vaccine” Trump’s “Operation Warp Speed” injections.
“Since January 1, in the laboratory, I’m seeing a 20-times
increase of endometrial cancers over what I see on an annual
basis,” Cole stated in the video.
“I’m not exaggerating at all because I look at my numbers year
over year, and I’m like ‘Gosh, I’ve never seen this many
endometrial cancers before.’”...
The horror of the Haitian migrant camp in Texas shows
why America MUST end its woke approach to immigration now
Over 3,000 Doctors and Scientists Sign Declaration
Accusing COVID Policy-Makers of ‘Crimes Against Humanity’
Dr Judy Mikowits can’t believe Fauci wasn’t arrested
forty years ago.
IS THERE A COVID VACCINE / CANCER CONNECTION?
Ron Kita's latest video re: electret levitation
The Spartacus letter
This is a very important 40 page letter that was posted
It was obviously written by someone in the know and despite it's
large size it is going viral. The PDF for this crashes so I am
putting the entire text on this page rather than linking a PDF
that will not work. I suspect sabotage on the PDF because TPTB
would want this shut down.
There are some encoding errors I have to go over and fix.
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
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
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.
�� COVID-19 is a blood and blood vessel disease. SARS-CoV-2
infects the lining of human blood vessels, causing them to leak
into the lungs.
* Current treatment protocols (e.g. invasive ventilation) are
actively harmful to patients, accelerating oxidative stress and
causing severe VILI (ventilator-induced lung injuries). The
continued use of ventilators in the absence of any proven medical
benefit constitutes mass murder.
* Existing countermeasures are inadequate to slow the spread of
what is an aerosolized and potentially wastewater-borne virus, and
constitute a form of medical theater.
* Various non-vaccine interventions have been suppressed by both
the media and the medical establishment in favor of vaccines and
expensive patented drugs.
* The authorities have denied the usefulness of natural immunity
against COVID-19, despite the fact that natural immunity confers
protection against all of the virus��s proteins, and not just one.
* Vaccines will do more harm than good. The antigen that these
vaccines are based on, SARS-CoV- 2 Spike, is a toxic protein.
SARS-CoV-2 may have ADE, or antibody-dependent enhancement;
current antibodies may not neutralize future strains, but instead
help them infect immune cells. Also, vaccinating during a pandemic
with a leaky vaccine removes the evolutionary pressure for a virus
to become less lethal.
* There is a vast and appalling criminal conspiracy that directly
links both Anthony Fauci and Moderna to the Wuhan Institute of
* 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
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
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
The breakdown of the pathology is as follows:
SARS-CoV-2 Spike binds to ACE2. Angiotensin Converting Enzyme 2 is
an enzyme that is part of the renin-angiotensin-aldosterone
system, or RAAS. The RAAS is a hormone control system that
moderates fluid volume in the body and in the bloodstream (i.e.
osmolarity) by controlling salt retention and excretion. This
protein, ACE2, is ubiquitous in every part of the body that
interfaces with the circulatory system, particularly in vascular
endothelial cells and pericytes, brain astrocytes, renal tubules
and podocytes, pancreatic islet cells, bile duct and intestinal
epithelial cells, and the seminiferous ducts of the testis, all of
which SARS-CoV-2 can infect, not just the lungs.
SARS-CoV-2 infects a cell as follows: SARS-CoV-2 Spike undergoes a
conformational change where the S1 trimers flip up and extend,
locking onto ACE2 bound to the surface of a cell. TMPRSS2, or
transmembrane protease serine 2, comes along and cuts off the
heads of the Spike, exposing the S2 stalk-shaped subunit inside.
The remainder of the Spike undergoes a conformational change that
causes it to unfold like an extension ladder, embedding itself in
the cell membrane. Then, it folds back upon itself, pulling the
viral membrane and the cell membrane together. The two membranes
fuse, with the virus's proteins migrating out onto the surface of
the cell. The SARS-CoV-2 nucleocapsid enters the cell, disgorging
its genetic material and beginning the viral replication process,
hijacking the cell s own structures to produce more virus.
SARS-CoV-2 Spike proteins embedded in a cell can actually cause
human cells to fuse together, forming syncytia/MGCs (multinuclear
giant cells). They also have other pathogenic, harmful effects.
SARS-CoV- 2's viroporins, such as its Envelope protein, act as
calcium ion channels, introducing calcium into infected cells. The
virus suppresses the natural interferon response, resulting in
delayed inflammation. SARS-CoV-2 N protein can also directly
activate the NLRP3 inflammasome. Also, it suppresses the Nrf2
antioxidant pathway. The suppression of ACE2 by binding with Spike
causes a buildup of bradykinin that would otherwise be broken down
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
Neutrophils have a nasty trick. They can also eject these enzymes
into the extracellular space, where they will continuously spit
out peroxide and bleach into the bloodstream. This is called
neutrophil extracellular trap formation, or, when it becomes
pathogenic and counterproductive, NETosis. In severe and critical
COVID-19, there is actually rather severe NETosis.
Hypochlorous acid building up in the bloodstream begins to bleach
the iron out of heme and compete for O2 binding sites. Red blood
cells lose the ability to transport oxygen, causing the sufferer
to turn blue in the face. Unliganded iron, hydrogen peroxide, and
superoxide in the bloodstream undergo the Haber- Weiss and Fenton
reactions, producing extremely reactive hydroxyl radicals that
violently strip electrons from surrounding fats and DNA, oxidizing
This condition is not unknown to medical science. The actual name
for all of this is acute sepsis.
We know this is happening in COVID-19 because people who have died
of the disease have noticeable ferroptosis signatures in their
tissues, as well as various other oxidative stress markers such as
nitrotyrosine, 4-HNE, and malondialdehyde.
When you intubate someone with this condition, you are setting off
a free radical bomb by supplying the cells with O2. It's a
catch-22, because we need oxygen to make Adenosine Triphosphate
(that is, to live), but O2 is also the precursor of all these
damaging radicals that lead to lipid peroxidation.
The correct treatment for severe COVID-19 related sepsis is
non-invasive ventilation, steroids, and antioxidant infusions.
Most of the drugs repurposed for COVID-19 that show any benefit
whatsoever in rescuing critically-ill COVID-19 patients are
antioxidants. N-acetylcysteine, melatonin, fluvoxamine,
budesonide, famotidine, cimetidine, and ranitidine are all
antioxidants. Indomethacin prevents iron- driven oxidation of
arachidonic acid to isoprostanes. There are powerful antioxidants
such as apocynin that have not even been tested on COVID-19
patients yet which could defang neutrophils, prevent lipid
peroxidation, restore endothelial health, and restore oxygenation
to the tissues.
Scientists who know anything about pulmonary neutrophilia, ARDS,
and redox biology have known or surmised much of this since March
2020. In April 2020, Swiss scientists confirmed that COVID-19 was
a vascular endotheliitis. By late 2020, experts had already
concluded that COVID-19 causes a form of viral sepsis. They also
know that sepsis can be effectively treated with antioxidants.
None of this information is particularly new, and yet, for the
most part, it has not been acted upon. Doctors continue to use
damaging intubation techniques with high PEEP settings despite
high lung compliance and poor oxygenation, killing an untold
number of critically ill patients with medical malpractice.
Because of the way they are constructed, Randomized Control Trials
will never show any benefit for any antiviral against COVID-19.
Not Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The
reason for this is simple; for the patients that they have
recruited for these studies, such as Oxford's ludicrous RECOVERY
study, the intervention is too late to have any positive effect.
The clinical course of COVID-19 is such that by the time most
people seek medical attention for hypoxia, their viral load has
already tapered off to almost nothing. If someone is about 10 days
post-exposure and has already been symptomatic for five days,
there is hardly any virus left in their bodies, only cellular
damage and derangement that has initiated a hyperinflammatory
response. It is from this group that the clinical trials for
antivirals have recruited, pretty much exclusively.
In these trials, they give antivirals to severely ill patients who
have no virus in their bodies, only a delayed hyperinflammatory
response, and then absurdly claim that antivirals have no utility
in treating or preventing COVID-19. These clinical trials do not
recruit people who are pre-symptomatic. They do not test
pre-exposure or post-exposure prophylaxis.
This is like using a defibrillator to shock only flatline, and
then absurdly claiming that defibrillators have no medical utility
whatsoever when the patients refuse to rise from the dead. The
intervention is too late. These trials for antivirals show
systematic, egregious selection bias. They are providing a
treatment that is futile to the specific cohort they are
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
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 is airborne. The WHO carried water for China by claiming
that the virus was only droplet- borne. Our own CDC absurdly
claimed that it was mostly transmitted by fomite-to-face contact,
which, given its rapid spread from Wuhan to the rest of the world,
would have been physically impossible.
The ridiculous belief in fomite-to-face being a primary mode of
transmission led to the use of surface disinfection protocols that
wasted time, energy, productivity, and disinfectant.
The 6-foot guidelines are absolutely useless. The minimum safe
distance to protect oneself from an aerosolized virus is to be 15+
feet away from an infected person, no closer. Realistically, no
public transit is safe.
Surgical masks do not protect you from aerosols. The virus is too
small and the filter media has too large of gaps to filter it out.
They may catch respiratory droplets and keep the virus from being
expelled by someone who is sick, but they do not filter a cloud of
infectious aerosols if someone were to walk into said cloud.
The minimum level of protection against this virus is quite
literally a P100 respirator, a PAPR/CAPR, or a 40mm NATO CBRN
respirator, ideally paired with a full-body tyvek or tychem suit,
gloves, and booties, with all the holes and gaps taped.
Live SARS-CoV-2 may potentially be detected in sewage outflows,
and there may be oral-fecal transmission. During the SARS outbreak
in 2003, in the Amoy Gardens incident, hundreds of people were
infected by aerosolized fecal matter rising from floor drains in
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
These modified Spike proteins then migrate to the surface of the
cell, where they are anchored in place by a transmembrane domain.
The adaptive immune system detects the non-human viral protein
being expressed by these cells, and then forms antibodies against
that protein. This is purported to confer protection against the
virus, by training the adaptive immune system to recognize and
produce antibodies against the Spike on the actual virus. The
J&J and AstraZeneca vaccines do something similar, but use an
adenovirus vector for genetic material delivery instead of a lipid
nanoparticle. These vaccines were produced or validated with the
aid of fetal cell lines HEK-293 and PER.C6, which people with
certain religious convictions may object strongly to.
SARS-CoV-2 Spike is a highly pathogenic protein on its own. It is
impossible to overstate the danger presented by introducing this
protein into the human body.
It is claimed by vaccine manufacturers that the vaccine remains in
cells in the shoulder, and that SARS- CoV-2 Spike produced and
expressed by these cells from the vaccine's genetic material is
harmless and inert, thanks to the insertion of prolines in the
Spike sequence to stabilize it in the prefusion conformation,
preventing the Spike from becoming active and fusing with other
cells. However, a pharmacokinetic study from Japan showed that the
lipid nanoparticles and mRNA from the Pfizer vaccine did not stay
in the shoulder, and in fact bioaccumulated in many different
organs, including the reproductive organs and adrenal glands,
meaning that modified Spike is being expressed quite literally all
over the place. These lipid nanoparticles may trigger anaphylaxis
in an unlucky few, but far more concerning is the unregulated
expression of Spike in various somatic cell lines far from the
injection site and the unknown consequences of that.
Messenger RNA is normally consumed right after it is produced in
the body, being translated into a protein by a ribosome. COVID-19
vaccine mRNA is produced outside the body, long before a ribosome
translates it. In the meantime, it could accumulate damage if
inadequately preserved. When a ribosome attempts to translate a
damaged strand of mRNA, it can become stalled. When this happens,
the ribosome becomes useless for translating proteins because it
now has a piece of mRNA stuck in it, like a lace card in an old
punch card reader. The whole thing has to be cleaned up and new
ribosomes synthesized to replace it. In cells with low ribosome
turnover, like nerve cells, this can lead to reduced protein
synthesis, cytopathic effects, and neuropathies.
Certain proteins, including SARS-CoV-2 Spike, have proteolytic
cleavage sites that are basically like little dotted lines that
say "cut here", which attract a living organism's own proteases
(essentially, molecular scissors) to cut them. There is a
possibility that S1 may be proteolytically cleaved from S2,
causing active S1 to float away into the bloodstream while leaving
the S2 "stalk" embedded in the membrane of the cell that expressed
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
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
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
SARS-CoV-2, like other betacoronaviruses, may have Dengue-like
ADE, or antibody-dependent enhancement of disease. For those who
aren't aware, some viruses, including betacoronaviruses, have a
feature called ADE. There is also something called Original
Antigenic Sin, which is the observation that the body prefers to
produce antibodies based on previously-encountered strains of a
virus over newly- encountered ones.
In ADE, antibodies from a previous infection become
non-neutralizing due to mutations in the virus's proteins. These
non-neutralizing antibodies then act as trojan horses, allowing
live, active virus to be pulled into macrophages through their Fc
receptor pathways, allowing the virus to infect immune cells that
it would not have been able to infect before. This has been known
to happen with Dengue Fever; when someone gets sick with Dengue,
recovers, and then contracts a different strain, they can get
very, very ill.
If someone is vaccinated with mRNA based on the Spike from the
initial Wuhan strain of SARS-CoV-2, and then they become infected
with a future, mutated strain of the virus, they may become
severely ill. In other words, it is possible for vaccines to
sensitize someone to disease.
There is a precedent for this in recent history. Sanofi's
Dengvaxia vaccine for Dengue failed because it caused immune
sensitization in people whose immune systems were Dengue-naive.
In mice immunized against SARS-CoV and challenged with the virus,
a close relative of SARS-CoV-2, they developed immune
sensitization, Th2 immunopathology, and eosinophil infiltration in
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
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
Ralph Baric is a virologist and SARS expert at UNC Chapel Hill in
North Carolina. This is who Anthony Fauci was referring to when he
insisted, before Congress, that if any gain-of-function research
was being conducted, it was being conducted in North Carolina.
This was a lie. Anthony Fauci lied before Congress. A felony.
Ralph Baric and Shi Zhengli are colleagues and have co-written
papers together. Ralph Baric mentored Shi Zhengli in his
gain-of-function manipulation techniques, particularly serial
passage, which results in a virus that appears as if it originated
naturally. In other words, deniable bioweapons. Serial passage in
humanized hACE2 mice may have produced something like SARS-CoV-2.
The funding for the gain-of-function research being conducted at
the Wuhan Institute of Virology came from Peter Daszak. Peter
Daszak runs an NGO called EcoHealth Alliance. EcoHealth Alliance
received millions of dollars in grant money from the National
Institutes of Health/National Institute of Allergy and Infectious
Diseases (that is, Anthony Fauci), the Defense Threat Reduction
Agency (part of the US Department of Defense), and the United
States Agency for International Development. NIH/NIAID contributed
a few million dollars, and DTRA and USAID each contributed tens of
millions of dollars towards this research. Altogether, it was over
a hundred million dollars.
EcoHealth Alliance subcontracted these grants to the Wuhan
Institute of Virology, a lab in China with a very questionable
safety record and poorly trained staff, so that they could conduct
gain-of-function research, not in their fancy P4 lab, but in a
level-2 lab where technicians wore nothing more sophisticated than
perhaps a hairnet, latex gloves, and a surgical mask, instead of
the bubble suits used when working with dangerous viruses. Chinese
scientists in Wuhan reported being routinely bitten and urinated
on by laboratory animals. Why anyone would outsource this
dangerous and delicate work to the People's Republic of China, a
country infamous for industrial accidents and massive explosions
that have claimed hundreds of lives, is completely beyond me,
unless the aim was to start a pandemic on purpose.
In November of 2019, three technicians at the Wuhan Institute of
Virology developed symptoms consistent with a flu-like illness.
Anthony Fauci, Peter Daszak, and Ralph Baric knew at once what had
happened, because back channels exist between this laboratory and
our scientists and officials.
December 12th, 2019, Ralph Baric signed a Material Transfer
Agreement (essentially, an NDA) to receive Coronavirus mRNA
vaccine-related materials co-owned by Moderna and NIH. It wasn't
until a whole month later, on January 11th, 2020, that China
allegedly sent us the sequence to what would become known as
SARS-CoV-2. Moderna claims, rather absurdly, that they developed a
working vaccine from this sequence in under 48 hours.
Stephane Bancel, the current CEO of Moderna, was formerly the CEO
of bioMerieux, a French multinational corporation specializing in
medical diagnostic tech, founded by one Alain Merieux. Alain
Merieux was one of the individuals who was instrumental in the
construction of the Wuhan Institute of Virology's P4 lab.
The sequence given as the closest relative to SARS-CoV-2, RaTG13,
is not a real virus. It is a forgery. It was made by entering a
gene sequence by hand into a database, to create a cover story for
the existence of SARS-CoV-2, which is very likely a
gain-of-function chimera produced at the Wuhan Institute of
Virology and was either leaked by accident or intentionally
The animal reservoir of SARS-CoV-2 has never been found.
This is not a conspiracy ��theory��. It is an actual criminal
conspiracy, in which people connected to the development of
Moderna's mRNA-1273 are directly connected to the Wuhan Institute
of Virology and their gain-of-function research by very few
degrees of separation, if any. The paper trail is well-
The lab-leak theory has been suppressed because pulling that
thread leads one to inevitably conclude that there is enough
circumstantial evidence to link Moderna, the NIH, the WIV, and
both the vaccine and the virus's creation together. In a sane
country, this would have immediately led to the world's biggest
RICO and mass murder case. Anthony Fauci, Peter Daszak, Ralph
Baric, Shi Zhengli, and Stephane Bancel, and their accomplices,
would have been indicted and prosecuted to the fullest extent of
the law. Instead, billions of our tax dollars were awarded to the
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
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
COVID-19 Vaccine Development and Links to Transhumanism:
This section deals with some more speculative aspects of the
pandemic and the medical and scientific establishment's reaction
to it, as well as the disturbing links between scientists involved
in vaccine research and scientists whose work involved merging
nanotechnology with living cells.
On June 9th, 2020, Charles Lieber, a Harvard nanotechnology
researcher with decades of experience, was indicted by the DOJ for
fraud. Charles Lieber received millions of dollars in grant money
from the US Department of Defense, specifically the military think
tanks DARPA, AFOSR, and ONR, as well as NIH and MITRE. His
specialty is the use of silicon nanowires in lieu of patch clamp
electrodes to monitor and modulate intracellular activity,
something he has been working on at Harvard for the past twenty
years. He was claimed to have been working on silicon nanowire
batteries in China, but none of his colleagues can recall him ever
having worked on battery technology in his life; all of his
research deals with bionanotechnology, or the blending of nanotech
with living cells.
The indictment was over his collaboration with the Wuhan
University of Technology. He had double- dipped, against the terms
of his DOD grants, and taken money from the PRC��s Thousand
Talents plan, a program which the Chinese government uses to bribe
Western scientists into sharing proprietary R&D information
that can be exploited by the PLA for strategic advantage.
Charles Lieber��s own papers describe the use of silicon nanowires
for brain-computer interfaces, or ��neural lace�� technology. His
papers describe how neurons can endocytose whole silicon nanowires
or parts of them, monitoring and even modulating neuronal
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速. 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
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
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
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.
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
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
The pandemic and its response served multiple purposes for the
�� Concealing a depression brought on by the usurious plunder of
our economies conducted by rentier-capitalists and absentee owners
who produce absolutely nothing of any value to society whatsoever.
Instead of us having a very predictable Occupy Wall Street Part
II, the Elites and their stooges got to stand up on television and
paint themselves as wise and all-powerful saviors instead of the
marauding cabal of despicable land pirates that they are.
�� Destroying small businesses and eroding the middle class.
�� Transferring trillions of dollars of wealth from the American
public and into the pockets of billionaires and special interests.
�� Engaging in insider trading, buying stock in biotech companies
and shorting brick-and-mortar businesses and travel companies,
with the aim of collapsing face-to-face commerce and tourism and
replacing it with e-commerce and servitization.
�� Creating a casus belli for war with China, encouraging us to
attack them, wasting American lives and treasure and driving us to
the brink of nuclear armageddon.
�� Establishing technological and biosecurity frameworks for
population control and technocratic- socialist ��smart cities��
where everyone��s movements are despotically tracked, all in
anticipation of widespread automation, joblessness, and food
shortages, by using the false guise of a vaccine to compel
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
Magnetism generated in 2D organic material by star-like
A 2D nanomaterial consisting of organic molecules linked to metal
atoms in a specific atomic-scale geometry shows non-trivial
electronic and magnetic properties due to strong interactions
between its electrons.
How To Make Your Own Super Battery - Copper Oxide
Perpetual Battery - Powered By Water
Combining sunlight and wastewater nitrate to make the
world’s No. 2 chemical ammonia
Researchers developed a new method that uses nitrate, one of the
most common groundwater contaminants, to supply nitrogen and
sunlight to electrify the reaction. The system produces nearly
100% ammonia with nearly zero hydrogen gas side reactions. The
reaction needs no fossil fuels and produces no carbon dioxide or
other greenhouse gases, and its use of solar power yields an
unprecedented solar-to-fuel efficiency, or STF, of 11%, which is
10 times better than any other state-of-the-art system to produce
ammonia (about 1% STF).
Combining sunlight and wastewater nitrate to make the world’s No.
Solar-driven electrochemical synthesis of ammonia
using nitrate with 11% solar-to-fuel efficiency – YouTube
Nishithan C. Kani et al, Solar-driven electrochemical
synthesis of ammonia using nitrate with 11% solar-to-fuel
efficiency at ambient conditions, Energy & Environmental
Science (2021). DOI: 10.1039/D1EE01879E
What in the World is Deagel.com? – Deagel.com:
America's Twilight Years - Catastrophic Climate
estabilization, Loss of the Rule of Law - Pt 5
Climate Change, Wildfires, Chaos In Big Cities
By Frosty Wooldridge
University of Bristol: COVID-19 Spike Protein
Binds to and Changes Cells in the Heart
The SARS-CoV-2 Spike protein disrupts human cardiac
pericytes function through CD147-receptor-mediated
signalling: a potential non-infective mechanism of
COVID-19 microvascular disease
Elisa Avolio, et al.
Severe coronavirus disease 2019 (COVID-19) manifests as a
life-threatening microvascular syndrome. The severe acute
respiratory syndrome coronavirus 2 (SARS-CoV-2) uses the Spike (S)
protein to engage with its receptors and infect host cells.
To date, it is still not known whether heart vascular pericytes
(PCs) are infected by SARS-CoV-2, and if the S protein alone
provokes PC dysfunction. Here, we aimed to investigate the effects
of the S protein on primary human cardiac PC signalling and
function. Results show, for the first time, that cardiac PCs are
not permissive to SARS-CoV-2 infection in vitro, whilst a
recombinant S protein alone elicits functional alterations in PCs.
This was documented as: (1) increased migration, (2) reduced
ability to support endothelial cell (EC) network formation on
Matrigel, (3) secretion of pro-inflammatory molecules typically
involved in the cytokine stormand (4) production of
pro-apoptotic factors responsible for EC death. Next, adopting a
blocking strategy against he S protein receptors
angiotensin-converting enzyme 2 (ACE2) and CD147, we discovered
that the S protein stimulates the
phosphorylation/activation of the
extracellular signal-regulated kinase 1/2
(ERK1/2) through the CD147 receptor, but not ACE2, in PCs. The
neutralisation of CD147, either using a blocking antibody or mRNA
silencing, reduced ERK1/2 activation and rescued PC function in
the presence of the S protein. In conclusion, our findings suggest
that circulating S protein prompts vascular PC dysfunction,
potentially contributing to establishing microvascular injury in
organs distant from the site of infection. This mechanism
may have clinical and therapeutic implications.
Dick Allgire: Death of Petrodollar –
All of the madness we see has nothing to do with public health
or Trump or Biden or Afghanistan. All of the madness we see has to
do with the imminent financial and governance reset. As Fitts
says, the Plandemic and the vaxx serve as “air cover” to distract
from the fact that the dollar is dead and that the government
entitlements we paid into will soon vanish – it’s also to
exterminate as many claimants to these entitlements as possible.
Clif High : Red lines ahead. Prepare.
The RUSSIAN- Tsar Bomba
The Matrix Resurrections – Official Trailer 1
The Story of Ivermectin
All American Doctors Threatened With Loss Of License
If They Try To Warn Patients Of The Truth
From the American Board of Family Medicine, The American Board
of Internal Medicine And The American Board of Pediatrics On The
Dissemination Of Misinformation By Board Certified Physicians
New Details Emerge About Coronavirus Research at
More than 900 pages of materials related to U.S.-funded
coronavirus research in China were released following a FOIA
lawsuit by The Intercept.
2021 ESTC Prev., Practical Methods for Electrostatic
Stimulation Upon Organic Growth, Griffin Brock
Weird WARNING Woo - Explorers' Guide to SciFi World
Clif High warning re: telepathic inducement to get injected
New Clif High: Darker Times – Old Paradigms Are
Collapsing with Sarah Westall
Dr. CHARLES HOFFE - Interview Highlights
What do you really know about the COVID Vaccine?
Doctors, scientists and whistleblowers all around the world are
organizing, doing interviews, holding press conferences, suing
their governments and doing all they can to expose the lies about
COVID19, to reveal several effective treatments and to warn about
the dangers of an untested "vaccine." They are being suppressed,
censored, targeted and maligned. Many point out that it is not
really a vaccine by scientific definition. It is a new technology
using messenger RNA that actually re-writes your human DNA. There
has NEVER been a successful mRNA vaccine though they have
attempted for 20 years to create one. In every case, animal trials
were done and when the animals were later exposed to the virus
they had a severe auto-immune reaction where their immune systems
attacked their own cells and organs. There was a very high
percentage of death. The COVID19 vaccine was rolled out prior to
"FDA Approval." It was only "allowed" due to an "emergency" based
on the lie that no other effective treatments existed. By their
own guidelines, an untested treatment may be used for "an
emergency" if no other treatment exists.
The clinical trials for this mRNA COVID "vaccine" are not
scheduled to be completed until 2023.
Health care professionals have shown that known, simple,
inexpensive and extremely effective treatments are
being used successfully and they are being censored. Furthermore,
we are being told that even
after "vaccination" we must still wear masks, practice social
distancing and maintain lockdowns.
Does this really make any sense to anybody?
If you didn't have a TV or a smart phone and didn't hear any news,
would you feel like you were living through a pandemic?