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6 Serious COVID Jab Side Effects You're Not Hearing About
The media doesn't dare mention these adverse effects, but you need to know they
are now being reported in massive numbers. And according to these two experts,
the worst is yet to come. Find out what makes the COVID shots such a threat to
long-term health.
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STORY AT-A-GLANCE
- “Worse Than the Disease: Reviewing Some Possible Unintended Consequences
of mRNA Vaccines Against COVID-19,” by Stephanie Seneff, Ph.D., and Dr. Greg
Nigh, is one of the most comprehensive descriptions of the many possible
unintended consequences of the mRNA gene transfer technologies incorrectly
referred to as “COVID vaccines”
- As of December 3, 2021, the U.S. Vaccine Adverse Event Reporting System
(VAERS) has logged 19,886 COVID jab related deaths. Pfizer — the only company
that the U.S. Food and Drug Administration has granted full licensing for an
as-yet unavailable COVID shot — accounts for 13,268 of them
- Calculations suggest VAERS COVID-related reports are underreported by a
factor of 41. That means that in the U.S. alone, the actual death toll may be
closer to 374,576. Including international deaths reported to VAERS would put
the death toll at 815,326
- Key side effects that are now being reported in massive numbers include
miscarriages, heart attacks, myopericarditis, thrombocytopenia (low platelet
count), shingles, Bell’s palsy and a variety of permanent disabilities, many of
which involve neurological dysfunction
- The side effects we now see being reported were entirely predictable based
on the known science detailed in Seneff’s and Nigh’s paper
MIT scientist Stephanie Seneff’s paper,1 “Worse Than the Disease: Reviewing
Some Possible Unintended Consequences of mRNA Vaccines Against COVID-19,”
published in the International Journal of Vaccine Theory, Practice and Research
in collaboration with Dr. Greg Nigh, is still one of the best, most
comprehensive descriptions of the many possible unintended consequences of the
mRNA gene transfer technologies incorrectly referred to as “COVID vaccines.”
December 9, 2021, their paper was reprinted in the Townsend Letter, the
Examiner of Alternative Medicine.2 Seneff, Ph.D., a senior research scientist
at MIT who has been conducting research at MIT for over five decades, has spent
a large portion of her career investigating the hazards and mechanisms of
action of glyphosate.
Her attention was diverted to the science of mRNA gene transfer technologies in
early 2020, when Operation Warp Speed was announced. As noted in her paper,
many factors that lacked precedent, yet were being implemented at breakneck
speed, included:
- The first-ever use of PEG in an injection
- The first-ever use of mRNA gene transfer technology against an infectious
agent
- The first-ever “vaccine” to make no clear claims about reducing infection,
transmissibility or death
- The first-ever coronavirus vaccine ever tested on humans (and previous
coronavirus vaccines all failed due to antibody-dependent enhancement, a
condition in which the antibodies actually facilitate infection rather than
defend against it)
- The first-ever use of genetically modified polynucleotides in the general
population
An Insanely Reckless Process
In a May 2021 interview with me, Seneff said:
“To have developed this incredibly new technology so quickly, and to skip so
many steps in the process of evaluating [its safety], it's an insanely reckless
thing that they've done. My instinct was that this is bad, and I needed to know
[the truth].
So, I really dug into the research literature by the people who've developed
these vaccines, and then more extensive research literature around those
topics. And I don't see how these vaccines can possibly be doing anything good
...”
At the time, just five months into the mass inoculation campaign, Seneff
suspected the COVID shots would end up killing far more people than the
infection itself. Today, a full year into it, the statistics are grim beyond
belief, proving her educated prediction to have been an astute one.
mRNA Jabs Are Shockingly Hazardous
As of December 3, 2021, the U.S. Vaccine Adverse Event Reporting System (VAERS)
has logged an astounding 927,738 COVID jab related adverse events, including
19,886 deaths.3 VAERS can receive reports from vaccine manufacturers and other
international sources, and if we exclude those, the death toll reported in U.S.
territories exclusively stands at 9,136.4
Of the total death reports, Pfizer — the only company that the U.S. Food and
Drug Administration has granted full licensing for an as-yet unavailable COVID
shot — accounts for the vast majority: 13,268, compared to 4,894 for Moderna,
1,651 for Janssen and 73 for an undisclosed brand.
Pfizer also accounts for the vast majority of hospitalizations post-injection,
and while those over the age of 66 make up the bulk of deaths, the 25-to-50 age
group accounts for most of the hospitalizations. Key side effects that are now
being reported in massive numbers include:5
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Miscarriages
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Heart problems such as heart attacks and myopericarditis
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Thrombocytopenia (low platelet count)
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Shingles
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Bell’s palsy
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A variety of permanent disabilities, many of which involve neurological
dysfunction
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All of these consequences were predicted by Seneff and Nigh in their paper,
which makes the events all the more tragic. Importantly, VAERS is notoriously
underreported, so the real-world impact of these shots is far greater than what
those data suggest.
The Cure Is Indeed Worse Than the Disease
Calculations6 performed by Steve Kirsch, executive director of the COVID-19
Early Treatment Fund, and his team of statisticians suggest VAERS COVID-related
reports are underreported by a factor of 41. This is a conservative estimate,
supported by calculations using a variety of sources besides VAERS itself.
That means that in the U.S. alone (using the data for U.S. territories only),
the actual death toll may be closer to 374,576 (including international deaths
reported to VAERS would put the death toll at 815,326), and those are deaths
that occurred within days or weeks post-injection.
As Seneff and Nigh explain in their paper, there’s overwhelming reason to
suspect that these gene transfer injections will have devastating impacts in
the long term, resulting in excess deaths over the next decade.
What’s more, it’s clear that the death toll from the COVID-19 infection itself
in the U.S. has been vastly exaggerated, as it’s based on positive PCR tests
and even mere suspicion of COVID in the absence of testing. Many died from
other causes and just happened to have a positive COVID test at the time of
death.
Kirsch estimates the real death tally from COVID-19 to be about 50% of the
reported number (which is likely conservative). This means about 380,000
Americans died from COVID-19 (rather than with COVID), whereas the COVID shots
may have killed more than 374,570 in the first 11 months alone.
Seneff suspects that in the next 10 to 15 years, we’ll see a dramatic spike in
prion diseases, autoimmune diseases, neurodegenerative diseases at younger
ages, and blood disorders such as blood clots, hemorrhaging, stroke and heart
failure.
As predicted in the title of Seneff’s paper, it seems the cure may indeed end
up being worse than the disease. This is particularly true for children and
young adults, who have either died or been permanently disabled by the shots by
the thousands, while having an extraordinarily low risk of dying from or being
seriously harmed by the infection itself.
Seneff suspects that in the next 10 to 15 years, we’ll see a dramatic spike in
prion diseases, autoimmune diseases, neurodegenerative diseases at younger
ages, and blood disorders such as blood clots, hemorrhaging, stroke and heart
failure.
The Spike Protein Is the Most Dangerous Part of SARS-CoV-2
The reason we’re seeing all these problems from the COVID shots is because they
program your cells to continuously produce SARS-CoV-2 spike protein, which we
now know is the most dangerous part of the virus. Many experts noted this from
the start, wondering what the vaccine developers could possibly be thinking,
selecting this as the antigen for their shots.
While the mRNA injections can cause harm in many different ways, one basic
problem is that they can overstimulate your immune system to the point of
failure. In summary, as your cells start producing the viral spike proteins,
your immune cells rally to mop up the proteins and dump them into your
lymphatic system. (This is why many report swollen lymph nodes under the arms.)
The antibody response is part of your humoral immunity. You also have cellular
immunity, which is part of your innate immune system. Your innate immune system
is very powerful. If you're healthy, it can clear viruses without ever
producing a single antibody. Antibodies are actually a second-tier effect when
your innate immune system fails.
The problem is that your innate immune system will not be activated and likely
will fail to protect you if you get a COVID-19 shot, because it’s bypassing all
of the areas where your innate immune system would be brought to bear.
Normally you breathe the virus in and stimulate the production secretory IgA
antibodies that protect your respiratory system. When you bypass that route of
exposure with a jab in the arm, no secretory IgA antibodies are produced,
leaving you susceptible to the infection.
As explained by Ronald Kostoff in an excellent December 8, 2021, Trial Site
News article, “COVID-19 ‘Vaccines’: The Wrong Bomb Over the Wrong Target at the
Wrong Time”:7
“An effective vaccine would focus on cellular immunity in the respiratory and
intestinal tract, in which secretory IgA is produced by your lymphocytes that
are located directly underneath the mucous membranes that line the respiratory
and intestinal tract.
The antibodies produced by these lymphocytes are ejected through and to the
surface of the linings. These antibodies are thus on site to meet air-borne
viruses and they may be able to prevent viral binding and infection of the
cells.
Unfortunately, the main inoculants used presently for COVID-19 focus on
antibodies (IgG and circulating IgA) that occur in the bloodstream. These
antibodies protect the internal organs of the body from infectious agents that
try to spread via the bloodstream.”
When you are injected with the COVID jab, your body will only induce IgG and
circulating IgA — not secretory IgA, and these types of antibodies do not
effectively protect your mucous membranes from SARS-CoV-2 infection. So, as
noted by Kostoff, the breakthrough infections we’re now seeing “confirm the
fundamental design flaws” of this gene transfer technology.
“A natural infection with SARS-CoV-2 (coronavirus) will in most individuals
remain localized to the respiratory tract,” Kostoff writes.8 “The vaccines used
presently cause cells deep inside our body to express the viral spike protein,
which they were never meant to do by nature.
Any cell which expresses this foreign antigen on its surface will come under
attack by the immune system, which will involve both IgG antibodies and
cytotoxic T-lymphocytes. This may occur in any organ, but the damage will be
most severe in vital organs.
We are seeing now that the heart is affected in many young people, leading to
myocarditis or even sudden cardiac arrest and death. In other words, we are
dropping the wrong bomb on the wrong target at the wrong time!”
In the end, your body will essentially believe that your innate immune system
has failed, which means it must bring in the backup cavalry. In essence, your
body is now overreacting to something that isn’t true. You’re not actually
infected with a virus and your innate immune system has not failed, but your
body is forced to respond as if both are true.
Effects Likely to Persist Long Term
What’s more, the synthetic RNA in the mRNA vaccines contains a nucleotide
called methyl-pseudouridine, which your body cannot break down, and the RNA is
programmed to trigger maximum protein production. So, we’re looking at
completely untested manipulation of RNA.
It is very important to recognize that this is a genetically engineered mRNA
for the spike protein. It is not identical to the spike protein mRNA that
SARS-Cov-2 produces. It’s been significantly altered to avoid being metabolized
by your body.
The spike protein your body produces in response to the COVID-19 vaccine mRNA
locks into your ACE2 receptor. This is because the genetically engineered new
spike protein has additional prolines inserted that prevent the receptors from
properly closing, which then cause you to downregulate ACE2. That’s partially
how you end up with problems such as pulmonary hypertension, ventricular heart
failure and stroke.9,10
As noted in a 2020 paper,11 there’s a “pivotal link” between ACE2 deficiency
and SARS-CoV-2 infection. People with ACE2 deficiency tend to be more prone to
severe COVID-19. The spike protein suppresses ACE2,12 making the deficiency
even worse. According to Seneff, the gene transfer injections essentially do
the same thing, and we still don’t know how long the effects last.
Manufacturers initially guessed the synthetic RNA might survive in the human
body for about six months. A more recent investigation found the spike protein
persisted in recovered COVID patients for 15 months.13
This raises the suspicion that the synthetic and more persistent mRNA in the
COVID shots may trigger spike protein production for at least as long, and
probably longer.14 What’s more, the number of spike proteins produced by the
shots is far greater than what you experience in natural infection.
As explained by Dr. Peter McCullough,15 this means that after your first shot,
your body will produce spike protein for at least 15 months. But, when you get
shot No. 2 a few weeks later, that shot will cause spike protein production to
go on for 15 months or longer. With shot No. 3 six months after that, you
produce spike protein for yet another 15 months.
With regular boosters, you may never rid your body of the spike protein. All
the while, it’s wreaking havoc with your biology. McCullough likens it to “a
permanent install of an inflammatory protein in the human body,” and
inflammation is at the heart of most if not all chronic diseases. There’s
simply no possible way for these gene transfer shots to improve public health.
They’re going to decimate it.
Long-Term Neurological Damage Is To Be Expected
In her paper,16 Seneff describes several key characteristics of the SARS-CoV-2
spike protein that suggests it acts as a prion. This could help explain why
we’re seeing so many neurological side effects from the shots. According to
Seneff, the spike protein produced by the COVID shot, due to the modifications
made, may actually make it more of a prion than the spike protein in the actual
virus, and a more effective one.
For a detailed technical description of this you can read through Seneff’s
paper, but the take-home message is that COVID-19 shots are instruction sets
for your body to make a toxic protein that will eventually wind up concentrated
in your spleen, from where prion-like protein instructions will be sent out,
radically increasing your risk of developing neurodegenerative diseases.
Lung, Heart and Brain Diseases Are Predictable Consequences
Seneff also goes into great detail describing how the spike protein acts as a
metabolic poison. While I recommend reading Seneff’s paper in its entirety,
I’ve extracted some key sections below, starting with how the spike protein can
trigger pathological damage leading to lung damage and heart and brain
diseases:17
“The picture is now emerging that SARS-CoV-2 has serious effects on the
vasculature in multiple organs, including the brain vasculature … In a series
of papers, Yuichiro Suzuki in collaboration with other authors presented a
strong argument that the spike protein by itself can cause a signaling response
in the vasculature with potentially widespread consequences.
These authors observed that, in severe cases of COVID-19, SARS-CoV-2 causes
significant morphological changes to the pulmonary vasculature … Furthermore,
they showed that exposure of cultured human pulmonary artery smooth muscle
cells to the SARS-CoV-2 spike protein S1 subunit was sufficient to promote cell
signaling without the rest of the virus components.
Follow-on papers showed that the spike protein S1 subunit suppresses ACE2,
causing a condition resembling pulmonary arterial hypertension (PAH), a severe
lung disease with very high mortality … The ‘in vivo studies’ they referred to
… had shown that SARS coronavirus-induced lung injury was primarily due to
inhibition of ACE2 by the SARS-CoV spike protein, causing a large increase in
angiotensin-II.
Suzuki et al. (2021) went on to demonstrate experimentally that the S1
component of the SARS-CoV-2 virus, at a low concentration … activated the
MEK/ERK/MAPK signaling pathway to promote cell growth. They speculated that
these effects would not be restricted to the lung vasculature.
The signaling cascade triggered in the heart vasculature would cause coronary
artery disease, and activation in the brain could lead to stroke. Systemic
hypertension would also be predicted. They hypothesized that this ability of
the spike protein to promote pulmonary arterial hypertension could predispose
patients who recover from SARS-CoV-2 to later develop right ventricular heart
failure.
Furthermore, they suggested that a similar effect could happen in response to
the mRNA vaccines, and they warned of potential long-term consequences to both
children and adults who received COVID-19 vaccines based on the spike protein.
An interesting study by Lei et. al. (2021) found that pseudovirus — spheres
decorated with the SARS-CoV-2 S1 protein but lacking any viral DNA in their
core — caused inflammation and damage in both the arteries and lungs of mice
exposed intratracheally.
They then exposed healthy human endothelial cells to the same pseudovirus
particles. Binding of these particles to endothelial ACE2 receptors led to
mitochondrial damage and fragmentation in those endothelial cells, leading to
the characteristic pathological changes in the associated tissue.
This study makes it clear that spike protein alone, unassociated with the rest
of the viral genome, is sufficient to cause the endothelial damage associated
with COVID-19. The implications for vaccines intended to cause cells to
manufacture the spike protein are clear and are an obvious cause for concern.”
The COVID Shots Activate Latent Viruses
As mentioned earlier, shingles infection is turning out to be a rather common
side effect of the COVID shot, and like the neurological, vascular and cardiac
damage we’re seeing, activation of latent viral infections was also predicted.
One reason why latent viral infections are cropping up in response to the shots
is because the shots disable your type I interferon pathway. A second reason is
because your immune system is overburdened trying to deal with the inflammatory
spike proteins flowing through your body. Something’s got to give, so latent
viruses are allowed to break through.
That’s not the end of your potential troubles, however, as these coinfections
may worsen or accelerate other conditions, such as Bell’s Palsy, myalgic
encephalomyelitis and chronic fatigue syndrome.
Herpes viruses, for example, have been implicated as a trigger of both AIDS18
and chronic fatigue syndrome.19 Some research suggests these diseases don’t
appear until viruses from different families partner up and the type 1
interferon pathway is disabled.
With all of that in mind, it seems inevitable that, long term, the COVID mass
injection campaign will result in an avalanche of a wide range of debilitating
chronic illnesses.
A true lover of wisdom has hands too busy to hold on to anything! He learns by
doing and every pebble in the path becomes her teacher! Oink
