In a refreshing
flash of honesty, Pfizer’s
website acknowledged that its COVID-19 vaccine is not FDA approved:
“The
Pfizer-BioNTech COVID-19 vaccine has not been approved or licensed by the U.S.
Food and Drug Administration (FDA), but has been authorized for emergency use
by FDA under an Emergency Use Authorization (EUA).”
In other words,
the vaccine is experimental. It has not completed the FDA’s standard safety
and efficacy testing and was only authorized for temporary emergency use. You
could be forgiven for not knowing that because government, media and medical
authorities have obscured this fact. The
New York Times stated the Pfizer and Modern COVID-19 vaccines are “approved
for full use.” Fact checker alert: False. John
Hopkins University claimed all vaccines must meet the FDA’s rigorous safety
and efficacy standards, but neglected to mention the emergency authorization is
based on a lesser, arbitrary standard. At a vaccine rollout event, the grandfatherly
Dr. Fauci proclaimed, “I feel extreme confidence in the safety and the efficacy
of this vaccine.” Okay, but it is still unapproved and experimental. The
question remains: Are the COVID-19 vaccines truly safe?
No Substitute for Time
It normally takes
10
to 15 years to develop and approve new vaccines. Years of testing are
needed to know the short- and long-term effects. There is no substitute for
time. Some adverse reactions, such as autoimmune diseases, infertility and
cancers, may take months or years to manifest. We also want to know how long
immunity lasts. Is it days, months, years? The COVID-19 vaccines were developed
and authorized in only a matter of months. Phase III trials spanned all of 10
weeks. Nobody truly knows how safe or effective the vaccines are because testing
was woefully shortened. We will not know until after the majority of our
population is vaccinated. If something goes terribly wrong, it will be too
late.
The new mRNA vaccine
technology used by Pfizer and Moderna has never been approved before for human
use (and still is not). In fact, these products are not even vaccines. A vaccine is a substance
that stimulates an immune reaction to create antibodies against a particular
disease. The mRNA technology uses genetic engineering to cause the cells in our
body to manufacture spike proteins of the coronavirus, provoking an
autoimmune-type reaction where our immune system attacks what our own cells are
making. What could possibly go wrong with that?
Adverse Events and PEG Allergies
We can look at
the CDC’s Vaccine Adverse Event Reporting
System (VAERS) for an idea of what has gone wrong so far. VAERS is a passive
or voluntary reporting system for vaccine reactions. Famously, a report
funded by the Department of Health and Human Services found it contained
less than 1% of adverse reactions. So, it is only a snapshot. From the COVID-19
vaccine’s introduction on 12/15/20 through 1/22/21 (5 weeks), VAERS reported 9,795
adverse reactions to the Pfizer and Moderna vaccines, including 285 deaths. (If
these represent only 1%, then the real figures may be closer to 979,500 adverse
events and 28,500 deaths.) Reactions ranged from headache, fatigue and nausea
to convulsions, seizures and anaphylactic shock. Most of the people who died
after vaccination were over age 65. I suspect the frail bodies of some elderly
cannot handle the stress of the vaccine and their bodies succumb. Officials
in Norway came to the same conclusion after 23 people died shortly after
receiving their first dose. Sadly, Idaho began vaccinating the elderly on Feb.
1 without regard for this grim risk.
We also know the majority of people
have antibodies against an ingredient in the vaccine, polyethylene glycol
(PEG), which may cause an allergic reaction. A small but nontrivial percentage
of people have high levels of PEG antibodies and are at risk of severe
reactions including anaphylactic shock, which can be fatal without immediate
medical intervention. If you decide to get the vaccine, get it near a hospital.
Even More Serious Safety Questions
Beyond what we
know about the vaccines, there is what we do not know.
Could the vaccines
alter DNA? Every cell in our bodies contains our unique DNA, the blueprint for
life. Cells transcribe portions of DNA to create messenger RNA (mRNA), which
ribosomes read like software code to manufacture proteins. The mRNA vaccines push
synthetic RNA into our cells and hijack the ribosomes to create spike proteins
of the coronavirus. This process of pushing mRNA into cells is called RNA
transfection. Gene editing technologies like CRISPR-Cas9
also use RNA transfection to genetically modify living cells. While the CDC
claims the vaccines do not alter DNA, it is at least concerning that
scientists also use the same technique to modify DNA. Personally, I am not satisfied
DNA mutation could not occur, even in an unexpected or unusual way.
Furthermore, Pfizer’s
clinical trial protocols stated: “No testing of the participant’s DNA will
be performed.” If they are not testing DNA, how can they definitively claim DNA
mutation does not occur?
Could the COVID-19
vaccines cause infertility? Pfizer
admits that an amino acid sequence in the coronavirus spike protein matches
the syncytin-1 protein found in human placentas and gametes
(sperm). Is it possible the vaccine will cause a person’s immune system to target
syncytin-1 in their reproductive system and cause infertility? Pfizer said no
but, again, did not test for it. With no hard science to back their denial, the
question remains open.
Could the
vaccines make COVID-19 symptoms worse through antibody-dependent
enhancement (ADE)? Previous attempts to develop vaccines for the SARS and
MERS coronaviruses failed during animal testing because the vaccinated
animals died when exposed to the wild virus. Instead of developing
antibodies that neutralized the viruses, the animals developed non-neutralizing
antibodies that paradoxically enhanced the viruses’ ability to enter cells and
spread and made the disease significantly worse. This is a known problem with coronaviruses
that was discovered in the 1960s when developing the Respiratory Syncytial
Virus (RSV) vaccine. During a human trial, vaccinated children were exposed to
the virus and 80% had to be hospitalized and two died because of an ADE effect.
Pfizer claims their vaccine creates neutralizing antibodies for COVID-19, but
what about the mutated strains popping up around the world? Could it become
non-neutralizing for one of them? If so, we would have a much more serious
pandemic on our hands – among the vaccinated.
Alternative Treatments – Is a Vaccine Necessary?
The question
should also be asked, do we need a vaccine at all? Despite the government and
media’s drumbeat of COVID-19 fearmongering, the survival rate for people not in
a nursing home is 99.74%.
The survival rate for people under 40 is 99.99%. By comparison, the Idaho
Emergency Operations Plan defines a pandemic as having less than 98.5%
survival rate, which only holds true for the vulnerable age group of people
over 70, especially those with serious health issues. This begs the question as
to why a more targeted approach to managing COVID-19 was not taken, instead of the
broad and destructive lockdowns and restrictions.
Most COVID-19
deaths and ICU admissions could have been avoided with common, inexpensive
medicines. Medical studies have long shown that vitamin D reduces the risk
and severity of
respiratory virus illnesses. Deficiency in vitamin D is associated with a 77%
increased risk of contracting COVID-19. A study in Spain found a 96%
reduction in ICU admissions for COVID-19 patients supplemented with vitamin
D. The region of Andalusia, Spain, distributed vitamin D to nursing home
residents and saw an
82% decrease in COVID-19 deaths. Why did the CDC never recommend it? My
family began supplementing vitamin D and C in January 2020 and then we all got
COVID-19 in June. For my youngest daughter, it was only one day of fatigue. My
wife and I, who are in our 40s, were back working out within a week,
thankfully.
There is a
mountain of scientific evidence that ivermectin
and hydroxychloroquine (paired with zinc)
are highly effective in preventing and curing COVID-19. These drugs are
off-patent and inexpensive. Dr. Fauci’s own National Institute of Health has
known since 2005 that chloroquine
could be effective against coronaviruses. More recently, Dr.
Pierre Kory testified in a senate hearing about the unbelievable results of
using ivermectin.
We had the
ability to treat COVID-19 all along, yet the FDA and CDC ignored these easy,
inexpensive treatments in favor of Operation Warp Speed, an $18 billion
boondoggle to rush experimental vaccines to market. I will leave it to the
reader to imagine the motivations and agendas behind this decision, though one
is glaringly obvious. There is little money to be made in vitamins and
off-patent drugs, but $$$ billions to be made in patented vaccines with the
government funding R&D and guaranteeing a huge market and zero product
liability for the pharmaceutical companies. As the saying goes, follow the
money.
Where Is Informed Consent?
In the wake of
the Nuremberg Trials after World War 2, the terrible medical experiments in
concentration camps inspired the creation of a set of ethical principles for
medical experimentation called the Nuremberg Code.
The cornerstone of this code is informed consent without duress. Let me ask: Were
you told the COVID-19 vaccines are experimental? Were you fully informed about
the risks of adverse reactions, both known and unknown? Were you informed that
effective alternative therapies exist? Do you feel pressure to take this
vaccine from your workplace or because of potential travel or other
restrictions?
People can make
their own decisions about taking these vaccines. But there is a grave violation
here on the part of medical and government authorities for failing to fully
inform.