Coronavirus pandemic 2019-20 #5

All the clowns running around claiming that less than 10 in a million are vax injured need to be drawn and quartered.

Worth highlighting from the JohninMK link above:

https://www.bitchute.com/video/6xIYPZBkydsu/

A new study has now surfaced, the results of which are terrifying.[25] A researcher at Kingston University in London, has completed an extensive analysis of the VAERs data (a subdepartment of the CDC which collects voluntary vaccine complication data), in which he grouped reported deaths following the vaccines according to the manufacturer’s lot numbers of the vaccines. Vaccines are manufactured in large batches called lots. What he discovered was that the vaccines are divided into over 20,000 lots and that one out of every 200 of these batches (lots) is demonstrably deadly to anyone who receives a vaccine from that lot, which includes thousands of vaccine doses.

He examined all manufactured vaccines—Pfizer, Moderna, Johnson and Johnson (Janssen), etc. He found that among every 200 batches of the vaccine from Pfizer and other makers, one batch of the 200 was found to be over 50x more deadly than vaccines batches from other lots. The other vaccine lots (batches) were also causing deaths and disabilities, but nowhere near to this extent. These deadly batches should have appeared randomly among all “vaccines” if it was an unintentional event. However, he found that 5% of the vaccines were responsible for 90% of the serious adverse events, including deaths. The incidence of deaths and serious complications among these “hot lots” varied from over 1000% to several thousand percent higher than comparable safer lots. If you think this was by accident—think again. This is not the first time “hot lots” were, in my opinion, purposefully manufactured and sent across the nation—usually vaccines designed for children. In one such scandal, “hot lots” of a vaccine ended up all in one state and the damage immediately became evident. What was the manufacture’s response? It wasn’t to remove the deadly batches of the vaccine. He ordered his company to scatter the hot lots across the nation so that authorities would not see the obvious deadly effect.

All lots of a vaccine are numbered—for example Modera labels them with such codes as 013M20A. It was noted that the batch numbers ended in either 20A or 21A. Batches ending in 20A were much more toxic than the ones ending in 21A. The batches ending in 20A had about 1700 adverse events, versus a few hundred to twenty or thirty events for the 21A batches. This example explains why some people had few or no adverse events after taking the vaccine while others are either killed or severely and permanently harmed. To see the researcher’s explanation, go to https://www.bitchute.com/video/6xIYPZBkydsu/ In my opinion these examples strongly suggest an intentional alteration of the production of the “vaccine” to include deadly batches.

Turdope making theater of getting a booster shot. In reality this is a saline shot.

The COVID Jabs’ Mechanisms of Injury
Analysis by Dr. Joseph Mercola
 Fact Checked
November 20, 2022
STORY AT-A-GLANCE
 In “Innate Immune Suppression by SARS-CoV-2 mRNA Vaccinations: The Role of G-
quadruplexes, Exosomes and MicroRNAs,” Stephanie Seneff, Ph.D., and Drs. Peter
McCullough, Greg Nigh and Anthony Kyriakopoulos explain how the COVID shots
suppress your innate immune function, and how they may cause neurological diseases
 Their landmark paper was the source of major controversy in that the prominent journal
in which it was published receive much negative feedback and the editor of the journal
was forced to resign although the paper has not been retracted at this time
 G4s are genome-wide targets of transcriptional regulation. The “G” stands for guanine.
G4 is DNA sequence of four consecutive guanines, which plays an important role in
diseases such as cancers and neurological disorders. The COVID jab spike protein
produces far more G-quadruplexes (G4) than the virus. The G4 causes prion protein to
misfold, which can result in prion diseases such as Creutzfeldt-Jakob disease and
Alzheimer’s
 Two specific microRNA have been found in people who got the jab, and these microRNA’s
interfere with Type 1 interferon response, which is a key part of your immune system.
When Type 1 interferon is suppressed, you become more prone to infection and chronic
disease
 The COVID jab produces high levels of immunoglobulin (IgG) antibodies, which are
associated with autoimmune disease. It does not produce mucosal antibodies
 Antibodies against the spike protein may be responsible for cases in which patients
developed highly aggressive prion disease after their second jabIn this interview, return guest Stephanie Seneff, Ph.D., a senior research scientist at MIT
for over five decades, 1 discusses her paper, 2 “Innate Immune Suppression by SARS-CoV-
2 mRNA Vaccinations: The Role of G-quadruplexes, Exosomes and MicroRNAs,”
published in the June 2022 issue of Food and Chemical Toxicology.
The paper was co-written with Drs. Peter McCullough, Greg Nigh and Anthony
Kyriakopoulos. In May 2021, Nigh and Seneff published a paper 3 detailing the
differences between the spike protein and the COVID jab spike protein.
In the “Innate Immune Suppression” paper, they and their other co-authors delve deep
into the mechanisms of the COVID shots, showing how they suppress your innate
immune system.
The paper caused quite a stir when it was first posted, prior to publication. A campaign
was launched to have it retracted on the premise that it would discourage people from
getting these life-saving shots — regardless of whether the mechanisms described were
true or not.
Ultimately, the controversy led to the resignation of the editor of the journal. Many have
also tried to discredit Seneff, and McCullough has since been stripped of his medical
credentials. 4
Understanding G-Quadruplexes
G-quadruplexes (G4) are genomewide targets of transcriptional regulation, and as such
as a novel target for drug design. The “G” in G4 stands for guanine, so G4 is DNA
sequence of four consecutive guanines. It’s one of the four nucleotides — the basic code
— in DNA, and it’s known to play an important role in diseases such as cancers and
neurological disorders. 5
As explained by Seneff, prions, when misfolded, build beta sheets and precipitate out of
the cytoplasm, causing plaque to form. This plaque is a hallmark of several
neurodegenerative diseases in animals and humans, such as Mad Cow disease,
Creutzfeldt-Jakob disease, scrapie (which affects deer) and Alzheimer’s disease.“So, there are all these debilitating neurodegenerative diseases that come out
of the prion protein, and the prion protein actually binds to its own G4s, which
are in its own RNA,” Seneff explains. “In so doing, it promotes [the prion protein]
to misfold into the wrong shape ... [which] causes prion disease.
The [COVID jabs] produce a version of the messenger RNA (mRNA) that codes
for the spike protein. Their version is enriched in guanines — it produces a lot
more G4s than the original mRNA that the virus produces — so, it's a different
form.
And there's lots of mRNA in the [COVID jab]. It's a big dose of this mRNA that is
enriched in G4s ... which then ... causes the cell to produce the prion protein.
So, the cell is producing the prion protein in the context of a situation with lots
of G4s lying around from the mRNA from vaccine. That's a really dangerous
situation for causing the prion protein to misfold and causing prion disease.”
How the COVID Jab Can Induce Autoimmune Disease
As explained by Seneff, the mRNA in the jab is taken into your lymph system and spleen,
germinal centers where antibodies are produced, and in order to produce the antibodies,
these germinal centers release exosomes. This can help explain the phenomenon of
“shedding,” but it also helps explain the immune destruction we see occurring. Seneff
explains:
“The exosomes are part of the process by which the cells communicate to
induce the antibody production, which is the goal of the [COVID jab]. The [jab]
does a fantastic job of producing high levels of IgG [immunoglobulin]
antibodies, which are the ones that are associated with autoimmune disease.
It doesn't make the mucosal antibodies. It makes IgG, which is actually much
more dangerous if there are too many antibodies. They can cause autoimmune
disease through molecular mimicry, and that's another aspect that I think is
going on.That's why you're getting this platelet problem where platelet count goes down
to zero, because you get antibodies to the platelets by molecular mimicry, or
even because the spike protein is binding to the platelets. They're getting
antibodies to the complex and you're wiping out the platelets.
Some people are getting thrombocytopenia and VITT [vaccine-induced immune
thrombotic thrombocytopenia], conditions that can be life-threatening. And
there's a huge signal for thrombosis. The paper talks about thrombosis. We
have ... seven tables for different aspects of the symptoms of the vaccine.
There's a table on the liver, there's a table on thrombosis, there's a table on
cancer, there's a table on the vagus nerve, and all of the inflammations of the
nerves because those exosomes are traveling up the vagus nerve, making their
way to the heart, brain and liver.
They're causing disease in all of those organs, and you see that very clearly in
the various databases — 98%, 99% of the [adverse event] reports in 2021 for
these conditions were [from the] COVID shots and 1% was all the other vaccines
combined.”
Mechanism of Action
Swiss researchers recently reported finding elevated troponin levels in 100% of COVID
jabbed individuals, indicating everyone is suffering some degree of heart damage, even
if they’re asymptomatic. 6,7 Seneff explains the mechanism by which the COVID shot
damages your heart.
“I think the whole issue is the spike protein being released by the immune cells
in the germinal centers — the lymph system and the spleen releasing these
exosomes that then travel along their fibers and reach all these critical organs.
The spleen has a very good connectivity with the liver, heart, brain and gut via
the nerve system, starting with the splanchnic nerve and then hooking up to the
vagus nerve ... So, these exosomes are migrating along the vagus nerve andthey're arriving at these organs and are getting taken up by cells there. And
everywhere they go, they cause inflammation.
The spike protein is very good at causing inflammation. That's been shown in
multiple studies ... It causes the immune cells to migrate to the heart, and that's
how you get myocarditis, this inflammation in the heart.
You also get inflammation in the muscles. I was looking at myositis, which is
muscle inflammation, and that's another issue. I've been in contact with
multiple people who suffered severe muscle damage from the spike protein,
even to the point of being debilitated because of [inflammation in the] muscles.
So, not just the heart, but the skeletal muscles are also affected in a really bad
way. Inflammation in the brain also causes neurons to be damaged and that's
causing cognitive disorders.
So, I think the long COVID is caused by the spike protein reaching the brain.
Many papers have talked about long COVID, and they think it's the spike protein,
not the virus, but the spike protein itself [that is causing it].”
The Role of MicroRNA
Another piece of the puzzle is related to the role of microRNA, which are embedded in
the exosomes that travel to the tissues. MicroRNA should not be confused with mRNA.
They’re two different things. The microRNAs are short pieces of RNA, about 22
nucleotides long. Unlike mRNA, microRNA do not code for protein.
The mRNA in the jabs are designed to be extremely resilient. Normally, mRNA lasts a
few hours, but the mRNA in the jabs stick around coding cells for several months, at
minimum primarily because of the substitution of the nucleotide uridine with
pseudouridine.
Because the mRNA is so resilient, spleen cells have to try to cope with all the spike
protein that they cannot stop making, and one way they do that is by pushing the spikeprotein out in the form of exosomes. Those exosomes also contain microRNAs. Indian
researchers found two specific microRNA in people who got the jab, and these
microRNAs interfere with Type 1 interferon response.
“This is a big topic of our paper,” Seneff says. “We talk about innate immune
suppression ... due to the effect of these microRNAs that are packaged up with
the spike protein.
Everywhere [the exosomes] go, they deliver these microRNAs, which disrupt the
immune cell's ability to respond to Type 1 interferon. These microRNAs actually
have a very high-level controlling element in the regulatory process of biology.
They control which genes are expressed.”
Hypothesis to Explain Post-Jab Sudden Death
Seneff goes on to cite animal research from 2005, in which mice were exposed to a
virus that causes myocarditis. They wanted to see what would happen if the mice were
suffering from myocarditis and then got a shot of adrenaline. So, the mice were infected
with the myocarditis-inducing virus, and then, 120 days later, they injected them with
adrenaline.
The dose given killed 70% of them. Meanwhile, control mice that did not have
myocarditis suffered no ill effect when injected with the same dose of adrenaline. The
mice that died, died of heart failure. Basically, their hearts were too damaged to
withstand the adrenaline rush. Today, we’re seeing a similar effect in athletes, who are
dropping dead while exerting themselves.
Digging for other papers, Seneff found one that detailed the Type 1 interferon response
in chromaffin cells, the cells that make adrenaline. Type 1 interferon inhibits and
reduces their production of adrenaline.
Seneff’s theory is that the COVID jabs interferes with your body’s ability to respond to
Type 1 interferon, thereby allowing too much adrenaline to be released. If your heart has
been damaged by the spike protein, the outcome could be lethal, as we’ve seen.“I think that could be what's going on with the sudden death problem, because
we certainly are seeing lots of young people dying of suddenly heart issues,”
she says.
At the same time, microthrombi (micro blood clots) are activated by the spike protein,
which could have lethal effects, and endothelial cells (the cells lining your blood
vessels) are also inflamed. So, there’s not just one mechanism by which the jabs could
kill you.
Spike Protein Creates Incredibly Tough Blood Clots
According to Seneff, blood clots are also connected to the prion aspect. Many different
proteins are amyloidogenic and can misfold, causing them to precipitate out, including
proteins in your blood. Blood clots are tough to break down, and when you add spike
protein into them, they become even tougher.
Seneff suspects the spike protein binds to fibrin, causing it then to misfold in a way that
makes it very resistant to breaking down. The same thing happens with prion proteins.
When they misfold, they create a gel that becomes denser over time, eventually
becoming completely inaccessible to the water base.
“It just precipitates out as this thing that just sits there for the rest of your life,”
Seneff says. “Nothing can get at it. The immune cells can't break it down. It just
stays there. It can't be cleared.”
This is why I recommend taking fibrinolytic enzymes like lumbrokinase (which is the
most effective), serrapeptase and nattokinase, several times a day one hour before or
two hours after a meal, if you’re struggling with long COVID, as they help break down the
fibrin. To work, you have to take them between meals, on an empty stomach, or else
they’ll just act as a digestive enzyme to break down food.
Another technique is to use a near-infrared sauna, which will help address the
misfolding of proteins by encouraging autophagy, your body’s natural clean-out process.The Role of Antibodies in Prion Disease
Antibodies may also play a role in the devastating side effects from the COVID jab. We
know that prion protein is upregulated in cells that produce it under stress, and the
COVID jab spike protein has been shown to cause cells to make more prion protein. One
possibility is that antibodies to a particular part of the spike protein end up binding to
the prion protein through molecular mimicry.
As explained by Seneff, researchers have discovered that if you produce antibodies to
the C-terminal end of the prion protein, it can cause disease that looks a lot like prion
disease but develops much faster.
As it turns out, the antibodies to the C-terminal end of the prion protein prevent the prion
protein from going into the endoplasmic reticulum (ER), where it needs to go in order to
do its job. Instead, the antibodies keep the prion in the cytoplasm.
Subsequently, the cell gets sick because of these antibodies. The late Luc Montagnier
posted a case study with 26 people who developed symptoms of prion disease within
the first month after their second vaccine. All died, many within three months of their
diagnosis. All were dead within a year, from what was basically an extremely aggressive
form of Creutzfeldt-Jakob disease (the human Mad Cow disease equivalent).
Seneff believes antibodies against the spike protein are to blame, because it didn’t
happen until they got their second dose. Antibodies developed after that first dose,
which primed the cells. Then, after the second dose the cells started making loads of
spike protein again, which the antibodies bound to.
This exosome package then traveled up the vagus nerve to the brain, where neurons
took them up. Seneff suspects this explains the disease process on those 26 patients.
“It would be explained completely by this model of spike protein antibodies
binding to the C-terminal domain and preventing the prion protein from going
into the ER,” she says, “and then, it causes [the prion protein] to break down.It gets broken down by the proteasome and disappears. So, it's causing a loss
of function problem for the prion protein in the neuron at a very accelerated
rate, much faster than what goes on with the normal prion disease ...
Montagnier and his team identified a segment of the spike protein that they
thought had characteristic prion-like features. Within that segment is a piece
that has five amino acids, YQRGS.
The prion protein has [the same] piece ... Except for the middle one, the other
four [amino acids] are all identical with this piece near the C-terminal end of the
prion protein. So, it's really perfect. It's a place where, if you get antibodies to
that, it’s basically a death sentence.”
How the COVID Jab Can Change Your Genome
Seneff, McCullough, Nigh and Kyriakopoulos recently posted yet another paper, 8
“Potential Mechanisms for Human Genome Integration of Genetic Code from SARS-
CoV-2 mRNA Vaccination,” describing how the mRNA in the COVID jab can change your
genome.
According to Big Pharma, public health agencies and “fact checkers,” the mRNA in the
jabs cannot integrate into human DNA. It’s impossible, they say. But science tells
another story. In fact, there’s more than one way in which this can happen.
For example, LINE-1, the human version of a retrovirus, is a very common piece of DNA
in the human genome, and it gets converted into RNA, which in turn codes for multiple
proteins that can cause the RNA to copy itself into another place in the DNA. It can also
copy and insert other RNA, such as the RNA in the COVID shot. This is a resource that
your cells have naturally. Seneff continues:
“The Alzheimer's brain has these neurons that have way too much DNA. It’s like
their genome is too big, and what they found is they have lots of extra copies of
the amyloid beta protein with different variations.It’s a way for the cell to ... try alternative forms of the protein that is not
working. That's what I think is going on. It's really quite fascinating because I
think that it provides the cell with the opportunity to fix a problem.
Let's say that it has a protein like amyloid beta that it's making and then that
protein is misbehaving. It's not working correctly. If ... it needs to make a
different version of [that protein], it can do that with LINE-1. Neurons express a
lot of LINE-1, and any cell that expresses LINE-1 has the opportunity to put that
spike protein RNA into the genome.”
In other words, the spike protein can hijack LINE-1, a system your body has that
integrates viral DNA into your DNA by using it to copy and insert its mRNA into the cell’s
DNA. There’s also another model. Nigh discovered research showing that double-
stranded DNA viruses, such as the herpes virus, have a mechanism for incorporating
human genes into its DNA.
It’s able to grab a hold of human RNA in the cytoplasm of the cell, convert it into DNA
and then insert it into its own genome. What this means is that certain viruses (such as
the herpes virus) could carry the genetic code for making spike protein, and it doesn’t
involve entering the nucleus of your cells at all.
COVID Jabs Impair Your Immune Function
To circle back to where we began, it seems the reason so many jabbed individuals are
now contracting COVID and other infections, and are dying from them, is because Type
1 interferon is suppressed. That suppresses your immune function, making you more
prone to contracting infections.
In the interview, Seneff also reviews how chronic exposure to glyphosate is a
predisposing condition for bad COVID-19 outcomes, as glyphosate disrupts the immune
system. For more details on that, please listen to the interview in its entirety. We also
review how glycine supplementation can help displace glyphosate in your body, thereby
limiting its damaging influence.To get a fuller, more in-depth grasp of the mechanisms by which the jabs injure your
health, I also recommend reading through “Innate Immune Suppression by SARS-CoV-2
mRNA Vaccinations: The Role of G-quadruplexes, Exosomes and MicroRNAs,” 9 and
“Potential Mechanisms for Human Genome Integration of Genetic Code from SARS-
CoV-2 mRNA Vaccination.” 10
Sources and References
1
MIT Stephanie Seneff Bio
2, 9
Food and Chemical Toxicology June 2022; 164: 113008
3 IJVTPR May 10, 2021: 2(1)
4 Rumble October 31, 2022
5 Cell Mol Life Science October 2021; 78(19-20): 6557-6583
6, 7
Daily Skeptic October 27, 2022
8, 10
Authorea September 1, 2022 DOI: 10.22541/au.166203678.82079667/v1

https://media.mercola.com/ImageServer/Public/2022/November/PDF/microrna-covid-vaccine-pdf.pdf

Just read a new report stating that we're quite possibly dealing with a 23k cases of myopericarditis per 1 million mRNA jabs.

That's not taking into account the multitude of other side effects related to the jabs.

At this point they'd have to physically hold me down to make me have one of their death jabs. I ain't taking that shit under any circumstance, thank you very much.

Study is from Thailand and is referred to by Dr McCullough in this video here. Again a myopericarditis rate of 2.3 percent.

https://mobile.twitter.com/_Janey_J/status/1593792088382005248

The Thai study I was made aware of recorded a minimum 6% injury rate (hypertension, heart irregularity, and various levels of heart damage).
I am not going to give these f*ckers any slack on their definition of what is an injury. I am still getting heart irregularities 7 months after
my single dose of alleged Novovax vaccine. The scumbags likely gave me an mRNA shot and claimed it was Novovax. Then why did they
not load the syringe from the actual vial and just brought out the filled syringe from a hidden location? I know that in ebil Rosshiya the
practice is to fill the syringe in front of the patient. Clearly this is not case in freedumb west.

Regarding the Mercola link above, how typical for these swine to attack the editor instead of debunking the research paper. This is the
"speed of science" today. A medieval, politically corrupt crime against humanity.

I would not rule this out. They know that people sceptical of the narrative would opt for options deemed 'safer' - like Novovax.

The psychology behind it is one of sociopaths. Think according to the lines of 'I had to endure the mRNA vaxx, so now you must too'.

Montagnier and his team identified a segment of the spike protein that theythought had characteristic prion-like features. Within that segment is a piece that has five amino acids, YQRGS. The prion protein has [the same] piece ... Except for the middle one, the other four [amino acids] are all identical with this piece near the C-terminal end of the prion protein. So, it's really perfect. It's a place where, if you get antibodies to that, it’s basically a death sentence.” wrote:

The vax spike protein is an engineered poison. It is intended to cause harm. This harm is enabled by corrupt regimes around the world
forcing mandates for "vaccination" even on people who have already recovered from covid infections and thus by definition do not need
any covid vaccine.

After making the mistake of submitting to a mandate to damage my health and getting the first dose, it was the smartest choice
for me to not take the second dose. It would have f*cked me up on another level or even killed me. I got an appointment with
a cardiologist but he was a gatekeeper and a statin-pusher fraud who fobbed off my vax injury as some sort of post-vax adrenaline
spike. This is the level of medical treatment in Turdope's Kanada. A toilet.

The Mengele swine are now trying to foist vax mandates for the flu.

A national emergency because of the flu.

This is beyond clown world.

I want to see the mandate maggots strung up with piano wire.

Read the comments: strokes galore. I should be happy that I did not get a stroke. Thank you Turdope!

The strokes indicate that the vax causes bleeding. This would be consistent with the heart injuries as well.

Previously pro vaxx doc does 180 after he sees 'turbo-cancers' skyrocket.

Scientists Revive 48,500-Year-Old 'Zombie Virus' Buried in Ice

https://www.ndtv.com/world-news/scientists-revive-48-500-year-old-zombie-virus-buried-in-ice-3562953

The fig leaf of science is transparent. No actual scientific value is obtained from playing around with semi-fossilized viruses. They are not
going to have some totally new type of genetic material (i.e. not DNA or RNA). So it is just pointless variation and we have active viruses
already that we can study to death.

Chinese anti-lockdown protesters earn the praise that Western ones never got

Establishment politicians and media outlets have praised the ‘freedom-loving’ Chinese, after demonizing those who spoke out against their own lockdowns.

https://www.rt.com/news/567493-china-covid-lockdown-protest/