John R. Houk, Blog Editor
© April 21, 2022
I recently know of a family member who decided to get the
Jab. Why the choice? It’s none of my business and neither is it your business.
What is interesting the family member passed out and was
taken to the hospital soon thereafter being released.
The family member was assured the Jab and the
unconsciousness had no relationship. The guess was perhaps a new diet and lack
of food caused the family member to pass out.
Here’s where it gets interesting to me. The blood sugar was
checked AND FOUND NORMAL. The blood pressure level was checked AND
FOUND NORMAL.
Interestingly, with otherwise normal vitals an EKG
was performed. I wondered to myself if the family member passed out from the
guess of a bad dietary intake, why was an EKG performed?
Here’s my non-medical guess based on the massive
Jab injuries documented (yet underreported).
Whoever the medical staff was (doctors and/or nurses – I really don’t know),
they probably lied about a dietary related fainting. My guess is the EKG was
related to Jab related concerns
of Myocarditis.
Below are science-truth cross post challenging the
science-lies of the Globalist-Fascist-Marxist New World Order.
JRH 4/21/22
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mRNA Vaccines Produce Persisting Spike Protein, Likely Causing Clots, Heart Inflammations, Cancers: Dr. Ryan Cole
By Harry Lee and Roman Balmakov
April 18, 2022 Updated: April 20, 2022
.jpg)
Dr. Ryan Cole in an
interview with The Epoch Times during the Global COVID-19 Summit at Houston,
Texas, on April 8, 2022. (York
Du/The Epoch Times)
According to Dr. Ryan Cole, messenger RNA (mRNA) vaccines
produce persisting spike protein that may cause severe damage to the
recipient’s health, such as unusual clotting, heart inflammation, or cancer.
Pfizer and Moderna COVID-19 vaccines are the only mRNA
vaccines approved or authorized for booster use in the United States. Johnson
& Johnson COVID-19 vaccines use a viral vector, a modified version of a
virus, to give cells instructions.
Cole is a pathologist who has operated a lab for 18 years.
He has seen, mostly through the microscope, about 500,000 patients in his
career.
“[In] normal mRNA, you have cells making messages all day
long … mRNA is generally broken down within minutes to maybe an hour or two.
mRNA should not persist,” Cole told EpochTV’s “Facts
Matter” program during the Global COVID Summit held in Houston,
Texas, on April 8.
Cole said mRNA is a message that tells your cell to make a
certain protein for different body reactions.
“But when you put this synthetic pseudouridine [in your
body],” said Cole. “The body doesn’t know what to do with it, and it looks at
it and says, ‘Hmm, I don’t know what to do. So I’m not going to break it down.’
And so it evades that breakdown process, and it also evades an immune response.
But it also turns down our immune system, which is not a good thing because
other things—cancers, viruses—get to wake up.”
In a February interview with The Epoch Times, Cole
said that he had seen an uptick in cancers that he shouldn’t be seeing. In
addition, he has seen elevations and clotting factors persisting for a long
time post-vaccination. However, when he voiced his concerns, no government
agencies were willing to look into this finding.
Currently, Cole examines about 40,000 biopsies a year.
Cole’s view aligns with Dr. Robert Malone, a key contributor
to mRNA vaccine technology. Malone, in an article published by The Epoch Times on April 11, said
the “mRNA” from the Pfizer and Moderna vaccines is not really mRNA. “These
molecules have genetic elements similar to those of natural mRNA, but they are
clearly far more resistant to the enzymes which normally degrade natural mRNA,
seem to be capable of producing high levels of protein for extended periods,
and seem to evade normal immunologic mechanisms for eliminating cells which
produce foreign proteins which are not normally observed in the body,” said
Malone.
Dr. Robert Malone in Washington
on June 29, 2021. (Zhen
Wang/The Epoch Times)
Dr. Joseph Mercola, an osteopathic physician, also said
the spike protein from the COVID-19 vaccines is to blame for the severe organ
damage.
“Science demonstrated that it wasn’t the virus causing endothelial
damage that led to organ damage, such as was found in the heart, liver, and
kidney of COVID-19 patients. Rather, it was the spike protein that was also
being injected in a genetic therapy shot program,” wrote Mercola in a recent article.
Some studies showed the vaccine-induced spike protein
persists in human bodies, said Cole, but “we have no idea how long that
synthetic sequence is persisting.”
A Stanford
study by Katharina Röltgen and others showed that the
synthetic sequence persists for at least 60 days. A Harvard study by Alana Ogata and others showed
that the spike protein could circulate for weeks.
Cole said a German professor, Dr. Arne Burkhardt, found
in his autopsy study that the spike protein could persist in the human body for
as long as 128 days.
“And the spike [protein] that [mRNA vaccines] make induces
pathologic changes in the body. It can cause clotting,” said Cole. “We hear
these young people dying from clots, micro clots, not normal types of clots.
These are a unique type of clot that persists, chokes off the body of oxygen,
chokes up body parts, inflames the heart, causes heart attacks, causes strokes,
causes cancers in young age groups … Unusual things that shouldn’t be happening
and are likely related to a synthetic, genetically modified sequence that we’re
putting into the bodies of billions of people.”
Cole said our cells have DNA-repair mechanisms, but the DNA
can’t repair itself when the spike protein gets into the nucleus of the
T-cells, one of the important white blood cells playing a central role in the
immune system.
“A study out of Sweden shows this,” said Cole, referring to
a recent study showing that mRNA from Pfizer’s
COVID-19 vaccine can enter human liver cells and be converted into DNA inside
the nucleus. “Now the cell, the DNA can’t repair itself. So the cell is going
to do one of two things, it’s either going to blow itself up, that’s called
apoptosis, or it’s going to mutate. And now it becomes an atypical malignant
cell.”
“To that question as well, the immune suppression because of
the spike [protein], because of the pseudouridine, it changes patterns of
receptors on cells,” said Cole, adding these receptors could enable T cells to
fight off all kinds of viruses.
“Now, you don’t have a defense system. This cancer cell can
invade over the wall. This pathogen can invade over the wall because your
immune system has been suppressed to a degree that allows that to happen. When
does that stop? We don’t know. How do we reverse it? We don’t know. Is it
happening to everybody? No, thank heavens. Is it happening to a degree that’s
alarming? You bet.”
A peer-reviewed study published on Apr. 15 also
found that mRNA vaccines “promote sustained synthesis of the SARS-CoV-2
spike protein” and “the spike protein is neurotoxic, and it impairs DNA repair
mechanisms.”
Neither Pfizer nor Moderna has responded to a request
for comment.
On its website, the Centers for Disease Control and
Prevention (CDC) states COVID-19 mRNA vaccines won’t affect or interact
with DNA, nor will the mRNA and the spike protein last long in the body.
“mRNA never enters the nucleus of the cell where our DNA
(genetic material) is located, so it cannot change or influence our genes,”
states the CDC. “Our cells break down mRNA and get rid of it within a few days
after vaccination. Scientists estimate that the spike protein, like other
proteins our bodies create, may stay in the body up to a few weeks.”
Intertwining Government-Corporate Interests
Cole said the vaccine manufacturers and government health
agencies knew about mRNA vaccines’ problems but hid it due to their
intertwining interests.
“We have known the immune modulation problems of this back
since 2006, at the very least some papers there,” said Cole. “There is a reason
Moderna had never brought an mRNA product to the market. And they had trials
for genetic disorders. They were going to use this modality for gene
modification. It never got to market because there were always too many animal
models’ side effects. They knew about this. Did Pfizer know about this? Yes.”
“[The Food and Drug Administration (FDA)] is
corporate-captured. Almost half of the FDA’s income and engrossing revenues
come from Pharma,” said Cole. “CDC has 57, 58 vaccine patents … Do you think
they have any interest in speaking ill of any vaccine? Of course not.
“The [National Institutes of Health (NIH)] holds the patent
to the spike protein and the sequence, and they licensed that to
Moderna. Every billion that the Moderna coffers get, so does the NIH. Is
that intertwining government-corporate interest? You bet.”
The Epoch Times has contacted the FDA, CDC, and NIH for
comments.
According to the FDA fact sheet, for fiscal year 2019, 54
percent of its budget was provided by federal budget authorization. The
remaining 46 percent, or $2.8 billion, was paid for by industry user fees.
The CDC lists over 60 “vaccine and therapeutic candidates”
technologies for licensing and collaboration on its website. The FDA has its own technology transfer program as well.
“Each year, hundreds of new inventions are made at NIH and
CDC laboratories. Nine NIH Institutes or Centers (ICs) transfer NIH and CDC
inventions through licenses to the private sector for further research and
development and eventual commercialization,” NIH said.
Model licensing agreements show these health
agencies ask for royalties to transfer their technologies.
According to Axios, in May 2020, then-NIH Director Francis
Collins said, “We do have some particular stake in the intellectual property”
behind Moderna’s coronavirus vaccine.
“Talking to the companies, I don’t hear any of them say they
think this [vaccine] is a money-maker,” Collins said. “Nobody sees this as a way
to make billions of dollars.”
.jpg)
Dr. Francis Collins, (L)
director of the National Institutes of Health, and Dr. Robert Redfield (R),
director of the Centers for Disease Control and Prevention, testify at a Senate
hearing in Washington on July 2, 2020. (Saul
Loeb-Pool/Getty Images)
“So nobody’s going to vote themselves out of a job in these
agencies,” said Cole. “By denying these applications and application fees and
drug reviews for all these large companies, they won’t have enough revenue to
keep their agency going either. It’s really a paradoxical lose-lose.”
“Truth plus transparency equals trust,” said Cole. However,
the government agencies are “destroying the public’s trust” in them.
Even the left-leaning New York Times recently reported that the CDC
is withholding critical COVID-19 data on boosters, hospitalizations, and other
analyses.
Cole said if he were in charge, he would have managed the
COVID response in line with the Great Barrington Declaration.
“We protect the vulnerable. We knew who this was going to
affect right away. We keep the schools wide open. We lock nobody down. We focus
on early treatments. We knew from SARS COVID-1 that chloroquines work against
this family of viruses. We go to old repurposed drugs like we always do with
any new and emerging disease. We treat early. We recognize those who are
COVID-recovered with natural immunity. And we don’t do what we did. You never
let the cure be worse than the disease itself.”
Harry Lee is a New York-based reporter for The Epoch Times. Contact Harry at harry.lee@epochtimes.com
Roman Balmakov
is a Reporter with The Epoch Times and host of the show, “Facts Matter.” He has
travelled around the country (as well as overseas) covering protests, riots,
and elections. He is also the producer of many Epoch Times’ commercials, both
on TV and social media.
Copyright © 2000 – 2022 The Epoch Times
++++++++++++++++
1000% Increase in Vaccine Deaths and Injuries Following
Pfizer COVID-19 EUA Vaccine for 5 to 11 Year Olds
Children-5-to-11-year-old-covid-vaccine-deaths
By Brian Shilhavy Editor, Health Impact News
April 16, 2022
Pfizer announced this week that they were asking the FDA to
issue an emergency use authorization (EUA) for a “booster” COVID-19 vaccine for
children between the ages of 5 and 11. (Source.)
The FDA issued an EUA for the first Pfizer COVID-19 shots
for this age group of children in October of 2021. (Source.)
At the time, a doctor on the FDA Advisory Committee
deliberating on whether or not an EUA should be given for this age group, stated
that the only way to find out if the Pfizer COVID-19 vaccines were safe for
this age group was to start injecting them with it.
“We’re never gonna learn about
how safe the vaccine is until we start giving it, and that’s just the way it
goes.”
Rumble VIDEO: Dr.
Ruben on the FDA panel can't verify the vaccine's safety
[Posted by Red Watch News
Published October 27, 2021
So now that we have almost 6 months of data since the first
EUA was issued for this age group to be injected with Pfizer’s COVID-19 shots,
just how safe is it?
So far over 10,000 cases have been filed to VAERS (Vaccine
Adverse Event Reporting System) of deaths and injuries among children in
this age group following the experimental COVID-19 vaccines. (Source.)
.jpg)
VAERS Data
for ages 5 - 11 (4/8/22)
By way of contrast, there have been 939 cases of vaccine
adverse events during this same time period for all of the FDA approved
vaccines for children in this age group. (Source.)
That means there has been an increase of over 1000% of
vaccine injuries and deaths for this age group following the COVID-19 vaccines.
.jpg)
VAERS
Data for ages 5 - 12 (4/8/22)
I could not find any data on how many children in this age
group have been injected with the Pfizer COVID-19 shots, but news reports have
stated that it is a small percentage of those eligible.
In California, for example, the LA Times reported that only
34% of children in this age group have taken the shots. (Source.)
For FDA approved vaccines in the childhood immunization
schedule, this age group receives the following vaccines: Diphtheria, tetanus,
& acellular pertussis vaccines, Inactivated poliovirus vaccine, Influenza
(one each year), Measles, mumps, rubella vaccines, Varicella vaccine, Tetanus,
diphtheria, & acellular pertussis vaccines, Human papillomavirus vaccine,
and the Meningococcal vaccine. (Source.)
I think it is safe to conclude, therefore, that these
children are receiving more FDA-approved vaccines than EUA COVID-19 vaccines.
Not only should the FDA not authorize a booster shot for
this age group, they should immediately suspend the original 2-dose Pfizer
COVID-19 vaccines for this age group.
As I have previously reported, however, it appears that
Pfizer is now in control of the FDA committing their crimes against humanity
with COVID-19 shots that are neither safe, nor effective.
Here are a few stories of children from this age group who
are now dead or crippled after taking one of these Pfizer shots.
… Photos
& Summaries of Jab Victims from this Point
Copyright 2022 Health Impact
News
Vaccine Impact HOMEPAGE
+++++++++++++++++++++++
More Than 1 Million COVID Vaccine Injuries, Nearly 27,000
Deaths Reported to VAERS, CDC Data Show
VAERS data released Friday by the Centers for Disease
Control and Prevention included a total of 1,226,314 reports of adverse events
from all age groups following COVID vaccines, including 26,976 deaths and
219,865 serious injuries between Dec. 14, 2020, and April 8, 2022.
4/15/22
The Centers for Disease Control and Prevention (CDC) today
released new data showing a total of 1,226,314
reports of adverse events following COVID vaccines were
submitted between Dec. 14, 2020, and April 8, 2022, to the Vaccine Adverse
Event Reporting System (VAERS). VAERS is the primary government-funded system
for reporting adverse vaccine reactions in the U.S.
The data included a total of 26,976
reports of deaths — an increase of 277 over the previous week
— and 219,865
serious injuries, including deaths, during the same time period —
up 2,564 compared with the previous week.
Excluding “foreign
reports” to VAERS, 805,921
adverse events, including 12,471
deaths and 79,811
serious injuries, were reported in the U.S. between Dec. 14, 2020,
and April 8, 2022.
Foreign
reports are reports foreign subsidiaries send to U.S. vaccine
manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a
manufacturer is notified of a foreign case report that describes an event that
is both serious and does not appear on the product’s labeling, the manufacturer
is required to submit the report to VAERS.
Of the 12,471 U.S. deaths
reported as of April 8, 17% occurred within 24 hours of
vaccination, 21% occurred within 48 hours of vaccination and 59% occurred in
people who experienced an onset
of symptoms within 48 hours of being vaccinated.
In the U.S., 564 million COVID vaccine doses had been
administered as of April 8, including 334
million doses of Pfizer, 212 million doses of Moderna and 19 million doses of
Johnson & Johnson (J&J).
VAERS
Chart thru 4/8/22 CHD.org
Every Friday, VAERS publishes
vaccine injury reports received as of a specified date. Reports submitted to
VAERS require further investigation before a causal relationship can be
confirmed.
Historically, VAERS has been shown to report only 1%
of actual vaccine adverse events.
U.S. VAERS data from Dec. 14, 2020, to April 8, 2022, for
5- to 11-year-olds show:
§
10,216
adverse events, including 242
rated as serious and 5
reported deaths.
§
18
reports of myocarditis and pericarditis (heart inflammation).
The CDC uses a narrowed
case definition of “myocarditis,” which excludes
cases of cardiac arrest, ischemic
strokes and deaths due to heart problems that occur before one
has the chance to go to the emergency department.
§
39
reports of blood clotting disorders.
U.S. VAERS data from Dec. 14, 2020, to April 8, 2022, for
12- to 17-year-olds show:
§
31,048
adverse events, including 1,792
rated as serious and 44
reported deaths.
§
67
reports of anaphylaxis among 12- to 17-year-olds where the
reaction was life-threatening, required treatment or resulted in death — with
96% of cases attributed to Pfizer’s
vaccine.
§
651
reports of myocarditis and pericarditis, with 639
cases attributed to Pfizer’s vaccine.
§
166
reports of blood clotting disorders, with all cases attributed
to Pfizer.
U.S. VAERS data from Dec. 14, 2020, to April 8, 2022, for
all age groups combined, show:
§
20% of deaths were related to cardiac disorders.
§
54% of those who died were male, 41% were female
and the remaining death reports did not include the gender of the deceased.
§
The average
age of death was 73.
§
As of April 8, 5,404
pregnant women reported adverse events related to COVID
vaccines, including 1,696 reports of miscarriage
or premature birth.
§
Of the 3,647
cases of Bell’s Palsy reported, 51% were attributed to Pfizer vaccinations,
40% to Moderna and
8% to J&J.
§
860 reports of Guillain-Barré
syndrome, with 42% of cases attributed
to Pfizer, 30% to Moderna and
28% to J&J.
§
2,373
reports of anaphylaxis where the reaction was
life-threatening, required treatment or resulted in death.
§
1,671
reports of myocardial infarction.
§
13,755
reports of blood-clotting disorders in the U.S. Of
those, 6,169
reports were attributed to Pfizer, 4,911
reports to Moderna and 2,654
reports to J&J.
§
4,124
cases of myocarditis and pericarditis with 2,531
cases attributed to Pfizer, 1,402
cases to Moderna and 181
cases to J&J’s COVID vaccine.
Woman develops fatal brain disease after second Moderna
dose
Carol Beauchine died from
sporadic Creutzfeldt-Jakob
Disease (CJD), a rapidly evolving, fatal degenerative
brain disorder she developed after her second dose of Moderna’s
COVID vaccine.
In an exclusive interview with The
Defender, Carol’s son, Jeffrey Beauchine, said it was excruciating
to watch his 70-year-old mother — who was healthy until she got the vaccine —
die from a disease he believes the vaccine caused.
Beauchine said Carol received her first dose of Moderna on
Feb. 16, 2021, and didn’t report any complaints. After getting the second dose
on March 17, Carol immediately said she “felt different.” She developed
numbness that spread throughout the entire left side of her body, blindness and
hearing loss. She lost the ability to walk and communicate, and her brain
degenerated until she passed away on Aug. 2, 2021 — just five months after
receiving her second dose of Moderna.
In an exclusive interview with The Defender, Jeffrey Beauchine said his mother, Carol, knew her Creutzfeldt-Jakob Disease was related to the Moderna shot. Watching her death was like “something you see out of a movie,” he said.https://t.co/z972KqtM9w
— Robert F. Kennedy Jr (@RobertKennedyJr) April 11, 2022
The family submitted a report to VAERS, but the CDC has not
followed up on Carol’s death. The Defender has
received numerous reports of people who died from sporadic CJD after receiving
a COVID vaccine — all women who were between the ages of 60 and 70,
including Cheryl
Cohen and Jennifer
Deason Sprague.
Biden administration extends COVID public health
emergency needed to keep vaccines under EUA
The Biden administration on Wednesday extended the
COVID public health emergency, now two years old, for an additional 90 days —
allowing vaccines and other drugs to remain under Emergency Use Authorization
(EUA). Keeping COVID vaccines and other countermeasures under EUA shields
pharmaceutical companies from liability for the harms caused
by their products.
According to Reuters,
a public health emergency was initially announced in January 2020, when the
COVID pandemic began. It has been renewed each quarter since and was due to
expire on April 16.
The Department of Health and Human Services (HHS) said in a
statement it was extending the public health emergency and will give states 60
days’ notice prior to termination or expiration. This may be the last time HHS
Secretary Xavier Becerra extends it, according to policy experts.
Pfizer to seek authorization from FDA for COVID booster
shot for kids 5 to 11 years old
Pfizer and BioNTech Thursday said they plan
to apply for EUA of a COVID booster dose for healthy 5- to
11-year-olds based on the results of a small study that has not been published
or analyzed by independent experts.
Pfizer said in a press
release the third dose of its vaccine produced significant
protection against the Omicron variant in children 5 to 11 in a small Phase 2/3
clinical trial. The study was based
on data from only 140 children 5 through 11 years old who received
a booster dose six months after the second dose of Pfizer-BioNTech’s COVID
vaccine as part of the primary series.
Pfizer claimed a closer look at 30 children showed a 36-fold
increase in virus-fighting antibodies — levels high enough to fight the Omicron
variant, and that a third dose was “well tolerated with no new safety signals
observed.”
Although Pfizer said more than 10,000 children under the age
of 12 have participated in clinical trials investigating Pfizer’s COVID
vaccine, only 140 were selected for the study forming the basis for the
company’s EUA request.
CDC launches internal review over failed COVID response
The CDC announced Monday
it was launching a month-long comprehensive agency-wide review following
widespread criticism of the agency’s response to the COVID pandemic.
The agency plans to evaluate its structure, systems and
processes, CDC Director Dr. Rochelle Walensky told staff in an email obtained
by The
Washington Post. Walensky said the goal of the review is to
“modernize” the agency and “to position CDC, and the public health community,
for greatest success in the future.”
The review will be conducted by Jim Mcrae, associate
administrator for primary healthcare at the Health Resources and Services
Administration (HRSA). The HRSA and the CDC are part of the Department of
Health and Human Services.
Last month, the CDC’s decision to remove
from its data tracker website tens of thousands of deaths
linked to COVID — including nearly a quarter of the deaths the agency said had
occurred among children — eroded public trust in the CDC’s handling of case
counts.
Children’s
Health Defense asks anyone who has experienced an adverse
reaction, to any vaccine, to file a report following these
three steps.
Megan Redshaw
is a staff attorney for Children's Health Defense and a reporter for The
Defender.
© 2016 - 2022 Children's Health Defense® •
All Rights Reserved.
The Defender HOMEPAGE
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