This article is a little too long for the format of this blog. It is nevertheless the best article I have found to date to explain the why and the how of the Covid pandemic.
Authored by Julius Ruechel via Julius Ruechel.com,
The Snake-Oil Salesmen and the COVID-Zero Con: A Classic Bait-And-Switch for a Lifetime of Booster Shots (Immunity as a Service)
If
a plumber with a lifetime of experience were to tell you that water
runs uphill, you would know he is lying and that the lie is not
accidental. It is a lie with a purpose. If you can also demonstrate that
the plumber knows in advance that the product he is promoting with that
lie is snake oil, you have evidence for a deliberate con. And once you
understand what's really inside that bottle of snake oil, you will begin
to understand the purpose of the con.
One of the most common
reasons given for mass COVID vaccinations is the idea that if we reach
herd immunity through vaccination, we can starve the virus out of
existence and get our lives back. It's the COVID-Zero strategy or some
variant of it.
By now it is abundantly clear from the epidemiological data that the vaccinated are able to both catch and spread the disease.
Clearly
vaccination isn't going to make this virus disappear. Only a mind that
has lost its grasp on reality can fail to see how ridiculous all this
has become.
But a tour through pre-COVID science demonstrates that, from day one, long before you and I had even heard of this virus, it was 100% inevitable and 100% predictable that
these vaccines would never be capable of eradicating this coronavirus
and would never lead to any kind of lasting herd immunity. Even
worse, lockdowns and mass vaccination have created a dangerous set of
circumstances that interferes with our immune system's ability to
protect us against other respiratory viruses. They also risk driving the
evolution of this virus towards mutations that are more dangerous to
both the vaccinated and the unvaccinated alike. Lockdowns, mass
vaccinations, and mass booster shots were never capable of delivering on
any of the promises that were made to the public.
And yet,
vaccination has been successfully used to control measles and even to
eradicate smallpox. So, why not COVID? Immunity is immunity, and a virus
is a virus is a virus, right? Wrong! Reality is far more complicated...
and more interesting.
This Deep Dive exposes why, from
day one, the promise of COVID-Zero can only ever have been a
deliberately dishonest shell game designed to prey on a lack of public
understanding of how our immune systems work and on how most respiratory
viruses differ from other viruses that we routinely vaccinate against.
We have been sold a fantasy designed to rope us into a pharmaceutical
dependency as a deceitful trade-off for access to our lives. Variant by
variant. For as long as the public is willing to go along for the ride.
Exposing
this story does not require incriminating emails or whistleblower
testimony. The story tells itself by diving into the long-established
science that every single virologist, immunologist, evolutionary
biologist, vaccine developer, and public health official had access to
long before COVID began. As is so often the case, the devil is hidden in
the details. As this story unfolds it will become clear that the
one-two punch of lockdowns and the promise of vaccines as an exit
strategy began as a cynical marketing ploy to coerce us into a
never-ending regimen of annual booster shots intentionally designed to
replace the natural "antivirus security updates" against respiratory
viruses that come from hugs and handshakes and from children laughing
together at school. We are being played for fools.
This is not to
say that there aren't plenty of other opportunists taking advantage of
this crisis to pursue other agendas and to tip society into a full-blown
police state. One thing quickly morphs into another. But this essay
demonstrates that never-ending boosters were the initial motive for this
global social-engineering shell game ― the subscription-based business
model, adapted for the pharmaceutical industry. "Immunity as a
service".
So, let's dive into the fascinating world of immune
systems, viruses, and vaccines, layer by layer, to dispel the myths and
false expectations that have been created by deceitful public health
officials, pharmaceutical lobbyists, and media manipulators. What
emerges as the lies are peeled apart is both surprising and more than a
little alarming.
“Once you eliminate the impossible, whatever remains, no matter how improbable, must be the truth.” - Sherlock Homes”
- Sir Arthur Conan Doyle
Table of Contents:
Viral Reservoirs: The Fantasy of Eradication
SARS: The Exception to the Rule?
Fast Mutations: The Fantasy of Control through Herd Immunity
Blind Faith in Central Planning: The Fantasy of Timely Doses
Spiked: The Fantasy of Preventing Infection
Antibodies, B-Cells, and T-Cells: Why Immunity to Respiratory Viruses Fades So Quickly
Manufacturing Dangerous Variants: Virus Mutations Under Lockdown Conditions — Lessons from the 1918 Spanish Flu
Leaky Vaccines, Antibody-Dependent Enhancement, and the Marek Effect
Anti-Virus Security Updates: Cross-Reactive Immunity Through Repeated Exposure
The Not-So-Novel Novel Virus: The Diamond Princess Cruise Ship Outbreak Proved We Have Cross-Reactive Immunity
Mother Knows Best: Vitamin D, Playing in Puddles, and Sweaters
The Paradox: Why COVID-Zero Makes People More Vulnerable to Other Viruses
Introducing Immunity as a Service - A Subscription-Based Business Model
for the Pharmaceutical Industry (It was always about the money!)
The Path Forward: Neutralizing the Threat and Bullet-Proofing Society to Prevent This Ever Happening Again.
* * *
Eradication
of a killer virus sounds like a noble goal. In some cases it is, such
as in the case of the smallpox virus. By 1980 we stopped vaccinating
against smallpox because, thanks to widespread immunization, we starved
the virus of available hosts for so long that it died out. No-one will
need to risk their life on the side effects of a smallpox vaccination
ever again because the virus is gone. It is a public health success
story. Polio will hopefully be next ― we're getting close.
But
smallpox is one of only two viruses (along with rinderpest) that have
been eradicated thanks to vaccination. Very few diseases meet the necessary criteria. Eradication is hard and only appropriate for very specific families of viruses.
Smallpox made sense for eradication because it was a uniquely human virus
― there was no animal reservoir. By contrast, most respiratory viruses
including SARS-CoV-2 (a.k.a. COVID) come from animal reservoirs: swine,
birds, bats, etc. As long as there are bats in caves, birds in ponds,
pigs in mud baths, and deer living in forests, respiratory viruses are
only controllable through individual immunity, but it is not possible to eradicate them. There will always be a near-identical cousin brewing in the wings.
Even the current strain of COVID is already cheerfully jumping onwards across species boundaries. According to both National Geographic and Nature magazine,
40% of wild deer tested positive for COVID antibodies in a study
conducted in Michigan, Illinois, New York, and Pennsylvania. It has also
been documented in wild mink and
has already made the species jump to other captive animals including
dogs, cats, otters, leopards, tigers, and gorillas. A lot of viruses are
not fussy. They happily adapt to new opportunities. Specialists, like
smallpox, eventually go extinct. Generalists, like most respiratory
viruses, never run out of hosts to keep the infection cycle going,
forever.
As long as we share this planet with other animals, it is
extremely deceitful to give anyone the impression that we can pursue
any scorched earth policy that can put this genie back in the bottle.
With an outbreak on this global scale, it was clear that we were always
going to have to live with this virus. There are over 200 other endemic
respiratory viruses that cause colds and flus, many of which circulate
freely between humans and other animals. Now there are 201. They will be
with us forever, whether we like it or not.
This
all sounds well and good, but the original SARS virus did disappear,
with public health measures like contact tracing and strict quarantine
measures taking the credit. However, SARS was the exception to the rule.
When it made the species jump to humans, it was so poorly adapted to
its new human hosts that it had terrible difficulty spreading. This very
poor level of adaptation gave SARS a rather unique combination of properties:
SARS was extremely difficult to catch (it was never very contagious)
SARS made people extremely sick.
SARS did not have pre-symptomatic spread.
These
three conditions made the SARS outbreak easy to control through contact
tracing and through the quarantine of symptomatic individuals. SARS
therefore never reached the point where it circulated widely among
asymptomatic community members.
By contrast, by January/February of 2020 it was clear from experiences in China, Italy, and the outbreak on the Diamond Princess cruise
ship (more on that story later) that the unique combination of
conditions that made SARS controllable were not going to be the case
with COVID. COVID was quite contagious (its rapid spread showed that
COVID was already well adapted to spreading easily among its new human
hosts), most people would have mild or no symptoms from COVID (making
containment impossible), and that it was spreading by aerosols produced
by both symptomatic and pre-symptomatic people (making contact tracing a joke).
In other words, it was clear by January/February 2020 that this pandemic would follow the normal rules of a readily transmissible respiratory
epidemic, which cannot be reined in the way SARS was. Thus, by
January/February of 2020, giving the public the impression that the SARS
experience could be replicated for COVID was a deliberate lie - this
genie was never going back inside the bottle.
Once
a reasonably contagious respiratory virus begins circulating widely in a
community, herd immunity can never be maintained for very long. RNA
respiratory viruses (such as influenza viruses, respiratory syncytial virus (RSV),
rhinoviruses, and coronaviruses) all mutate extremely fast compared to
viruses like smallpox, measles, or polio. Understanding the difference
between something like measles and a virus like COVID is key to
understanding the con that is being perpetrated by our health
institutions. Bear with me here, I promise not to get too technical.
All
viruses survive by creating copies of themselves. And there are always a
lot of "imperfect copies" — mutations — produced by the copying process
itself. Among RNA respiratory viruses these mutations stack up so
quickly that there is rapid genetic drift, which continually produces
new strains. Variants are normal. Variants are expected. Variants make
it virtually impossible to build the impenetrable wall of long-lasting
herd immunity required to starve these respiratory viruses out of
existence. That's one of several reasons why flu vaccines don't provide
long-lasting immunity and have to be repeated annually ― our immune
system constantly needs to be updated to keep pace with the inevitable
evolution of countless unnamed "variants."
This never-ending
conveyor belt of mutations means that everyone's immunity to COVID was
always only going to be temporary and only offer partial cross-reactive
protection against future re-infections. Thus, from day one, COVID
vaccination was always doomed to the same fate as the flu vaccine ― a
lifelong regimen of annual booster shots to try to keep pace with
"variants" for those unwilling to expose themselves to the risk of a
natural infection. And the hope that by the time the vaccines (and their
booster shots) roll off the production line, they won't already be out
of date when confronted by the current generation of virus mutations.
Genetic drift caused by mutations is much slower
in viruses like measles, polio, or smallpox, which is why herd immunity
can be used to control these other viruses (or even eradicate them as
in the case of smallpox or polio). The reason the common respiratory
viruses have such rapid genetic drift compared to these other viruses
has much less to do with how many errors are produced during the copying
process and much more to do with how many of those "imperfect" copies are actually able to survive and produce more copies.
A
simple virus with an uncomplicated attack strategy for taking over host
cells can tolerate a lot more mutations than a complex virus with a
complicated attack strategy. Complexity and specialization put limits on
how many of those imperfect copies have a chance at becoming successful
mutations. Simple machinery doesn't break down as easily if there is an
imperfection in the mechanical parts. Complicated high-tech machinery
will simply not work if there are even minor flaws in precision parts.
For
example, before a virus can hijack the DNA of a host cell to begin
making copies of itself, the virus needs to unlock the cell wall to gain
entry. Cellular walls are made of proteins and are coated by sugars;
viruses need to find a way to create a doorway through that protein
wall. A virus like influenza uses a very simple strategy to get inside ―
it locks onto one of the sugars on the outside of the cell wall in
order to piggyback a ride as the sugar is absorbed into the cell (cells
use sugar as their energy source). It's such a simple strategy that it
allows the influenza virus to go through lots of mutations without
losing its ability to gain entry to the cell. Influenza's simplicity
makes it very adaptable and allows many different types of mutations to
thrive as long as they all use the same piggyback entry strategy to get
inside host cells.
By contrast, something like the measles virus
uses a highly specialized and very complicated strategy to gain entry to
a host cell. It relies on very specialized surface proteins to break
open a doorway into the host cell. It's a very rigid and complex system
that doesn't leave a lot of room for errors in the copying process. Even
minor mutations to the measles virus will cause changes to its surface
proteins, leaving it unable to gain access to a host cell to make more
copies of itself. Thus, even if there are lots of mutations, those
mutations are almost all evolutionary dead ends, thus preventing genetic
drift. That's one of several reasons why both a natural infection and
vaccination against measles creates lifetime immunity ― immunity lasts
because new variations don't change much over time.
Most RNA
respiratory viruses have a high rate of genetic drift because they all
rely on relatively simple attack strategies to gain entry to host cells.
This allows mutations to stack up quickly without becoming evolutionary
dead ends because they avoid the evolutionary trap of complexity.
Coronaviruses
use a different strategy than influenza to gain access to host cells.
They have proteins on the virus surface (the infamous S-spike protein,
the same one that is mimicked by the vaccine injection), which latches
onto a receptor on the cell surface (the ACE2 receptor) ― a kind of key
to unlock the door. This attack strategy is a little bit more
complicated than the system used by influenza, which is probably why
genetic drift in coronaviruses is slightly slower than in influenza, but
it is still a much much simpler and much less specialized system than
the one used by measles. Coronaviruses, like other respiratory viruses,
are therefore constantly producing a never-ending conveyor belt of
"variants" that make long-lasting herd immunity impossible. Variants are
normal. The alarm raised by our public health authorities about
"variants" and the feigned compassion of pharmaceutical companies as
they rush to develop fresh boosters capable of fighting variants is a
charade, much like expressing surprise about the sun rising in the East.
Once
you got immunity to smallpox, measles, or polio, you had full
protection for a few decades and were protected against severe illness
or death for the rest of your life. But for fast-mutating respiratory
viruses, including coronaviruses, within a few months they are
sufficiently different that your previously acquired immunity will only
ever offer partial protection against your
next exposure. The fast rate of mutation ensures that you never catch
the exact same cold or flu twice, just their closely related constantly
evolving cousins. What keeps you from feeling the full brunt of each new
infection is cross-reactive immunity, which is another part of the story of how you are being conned, which I will come back to shortly.
But
let's pretend for a moment that a miraculous vaccine could be developed
that could give us all 100% sterilizing immunity today. The length of
time it takes to manufacture and ship 8 billion doses (and then make
vaccination appointments for 8 billion people) ensures that by the time
the last person gets their last dose, the never-ending conveyor belt of
mutations will have already rendered the vaccine partially ineffective.
True sterilizing immunity simply won't ever happen with coronaviruses.
The logistics of rolling out vaccines to 8 billion people meant that
none of our vaccine makers or public health authorities ever could have
genuinely believed that vaccines would create lasting herd immunity
against COVID.
So, for a multitude of reasons, it was a deliberate
lie to give the public the impression that if enough people take the
vaccine, it would create lasting herd immunity. It was 100% certain,
from day one, that by the time the last dose is administered, the rapid
evolution of the virus would ensure that it would already be time to
start thinking about booster shots. Exactly like the flu shot. Exactly
the opposite of a measles vaccine. Vaccines against respiratory viruses
can never provide anything more than a temporary cross-reactive immunity "update" ―
they are merely a synthetic replacement for your annual natural
exposure to the smorgasbord of cold and flu viruses. Immunity as a
service, imposed on society by trickery. The only question was always,
how long between booster shots? Weeks, months, years?
Feeling conned yet?
The
current crop of COVID vaccines was never designed to provide
sterilizing immunity - that's not how they work. They are merely a tool
designed to teach the immune system to attack the S-spike protein,
thereby priming the immune system to reduce the severity of
infection in preparation for your inevitable future encounter with the
real virus. They were never capable of preventing infection, nor of
preventing spread. They were merely designed to reduce your chance of
being hospitalized or dying if you are infected. As former FDA commissioner Scott Gottlieb, who is on Pfizer’s board, said: "the
original premise behind these vaccines were [sic] that they would
substantially reduce the risk of death and severe disease and
hospitalization. And that was the data that came out of the initial
clinical trials.” Every first-year medical student knows that you cannot get herd immunity from a vaccine that does not stop infection.
In
other words, by their design, these vaccines can neither stop you from
catching an infection nor stop you from transmitting the infection to
someone else. They were never capable of creating herd immunity. They
were designed to protect individuals against severe outcomes if they
choose to take them - a tool to provide temporary focused protection for
the vulnerable, just like the flu vaccine. Pushing for mass vaccination
was a con from day one. And the idea of using vaccine passports to
separate the vaccinated from the unvaccinated was also a con from day
one. The only impact these vaccine passports have on the pandemic is as a
coercive tool to get you to roll up your sleeve. Nothing more.
There
are multiple interconnected parts to why immunity to COVID, or any
other respiratory virus, is always only temporary. Not only is the virus
constantly mutating but immunity itself fades over time, not unlike the
way our brains start forgetting how to do complicated math problems
unless they keep practicing. This is true for both immunity acquired
through natural infection and immunity acquired through vaccination.
Our
immune systems have a kind of immunological memory ― basically, how
long does your immune system remember how to launch an attack against a
specific kind of threat. That memory fades over time. For some vaccines,
like diphtheria and tetanus, that immunological memory fades very slowly.
The measles vaccine protects for life. But for others, like the flu
vaccine, that immunological memory fades very quickly.
On average,
the flu vaccine is only about 40% effective to begin with. And it
begins to fade almost immediately after vaccination. By about 150 days
(5 months), it reaches zero.
Fading immunity after flu shot (Science, April 18th, 2019)
The
solution to this strange phenomenon lies in the different types of
immune system responses that are triggered by a vaccine (or by exposure
to the real thing through a natural infection). This has big
implications for coronavirus vaccines, but I'll get to that in a moment.
First a little background information...
A good analogy is to
think of our immune system like a medieval army. The first layer of
protection began with generalists - guys armed with clubs that would
take a swing at everything - they were good for keeping robbers and
brigands at bay and for conducting small skirmishes. But if the attack
was bigger, then these generalists were quickly overwhelmed, serving as
arrow fodder to blunt the attack on the more specialized troops coming
up behind them. Spearmen, swordsmen, archers, cavalry, catapult
operators, siege tower engineers, and so on. Each additional layer of
defense has a more expensive kit and takes ever greater amounts of time
to train (an English longbowman took years to build up the necessary
skill and strength to become effective). The more specialized a troop
is, the more you want to hold them back from the fight unless it's
absolutely necessary because they are expensive to train, expensive to
deploy, and make a bigger mess when they fight that needs to be cleaned
up afterwards. Always keep your powder dry. Send in the arrow fodder
first and slowly ramp up your efforts from there.
Our immune
system relies on a similar kind of layered system of defense. In
addition to various non-specific rapid response layers that take out the
brigands, like natural killer cells, macrophages, mast cells, and so
on, we also have many adaptive (specialized) layers of antibodies (i.e.
IgA, IgG, IgM immunoglobulin) and various types of highly specialized
white blood cells, like B-cells and T-cells. Some antibodies are
released by regular B-cells. Others are released by blood plasma. Then
there are memory B-cells, which are capable of remembering previous
threats and creating new antibodies long after the original antibodies
fade away. And there are various types of T-cells (again with various
degrees of immunological memory), like natural killer T-cells, killer
T-cells, and helper T-cells, all of which play various roles in
detecting and neutralizing invaders. In short, the greater the threat,
the more troops are called into the fight.
This is clearly a gross
oversimplification of all the different interconnected parts of our
immune system, but the point is that a mild infection doesn't trigger as
many layers whereas a severe infection enlists the help of deeper
layers, which are slower to respond but are much more specialized in
their attack capabilities. And if those deeper adaptive layers get
involved, they are capable of retaining a memory of the threat in order
to be able to mount a quicker attack if a repeat attack is recognized in
the future. That's why someone who was infected by the dangerous
Spanish Flu in 1918 might still have measurable T-cell immunity a
century later but the mild bout of winter flu you had a couple of years
ago might not have triggered T-cell immunity, even though both may have
been caused by versions of the same H1N1 influenza virus.
As a
rule of thumb, the broader the immune response, the longer immunological
memory will last. Antibodies fade in a matter of months, whereas B-cell
and T-cell immunity can last a lifetime.
Another rule of thumb is
that a higher viral load puts more strain on your immune defenses, thus
overwhelming the rapid response layers and forcing the immune system to
enlist the deeper adaptive layers. That's why nursing homes and
hospitals are more dangerous places for vulnerable people than backyard
barbeques. That's why feedlot cattle are more vulnerable to viral
diseases than cattle on pasture. Viral load matters a lot to how easily
the generalist layers are overwhelmed and how much effort your immune
system has to make to neutralize a threat.
Where the infection
happens in the body also matters. For example, an infection in the upper
respiratory tract triggers much less involvement from your adaptive
immune system than when it reaches your lungs. Part of this is because
your upper respiratory tract is already heavily preloaded with large
numbers of generalist immunological cells that are designed to attack
germs as they enter, which is why most colds and flus never make it
deeper into the lungs. The guys with the clubs are capable of handling
most of the threats that try to make through the gate. Most of the
specialized troops hold back unless they are needed.
Catching a
dangerous disease like measles produces lifetime immunity because an
infection triggers all the deep layers that will retain a memory of how
to fight off future encounters with the virus. So does the measles
vaccine. Catching a cold or mild flu generally does not.
From an
evolutionary point of view, this actually makes a lot of sense. Why
waste valuable resources developing long-lasting immunity (i.e. training
archers and building catapults) to defend against a virus that did not
put you in mortal danger. A far better evolutionary strategy is to
evolve a narrower generalist immune response to mild infections (i.e.
most cold and flu viruses), which fades quickly once the threat is
conquered, but invest in deep long-term broad-based immunity to
dangerous infections, which lasts a very long time in case that threat
is ever spotted on the horizon again. Considering the huge number of
threats our immune systems face, this strategy avoids the trap of
spreading immunological memory too thin. Our immunological memory
resources are not limitless - long-term survival requires prioritizing
our immunological resources.
The take-home lesson is that vaccines
will, at best, only last as long as immunity acquired through natural
infection and will often fade much faster because the vaccine is often
only able to trigger a partial immune response compared to the actual
infection. So, if the disease itself doesn't produce a broad-based
immune response leading to long-lasting immunity, neither will the
vaccine. And in most cases, immunity acquired through vaccination will
begin to fade much sooner than immunity acquired through a natural
infection. Every vaccine maker and public health official knows this despite
bizarrely claiming that the COVID vaccines (based on re-creating the
S-protein spike instead of using a whole virus) would somehow become the
exception to the rule. That was a lie, and they knew it from day one. That should set your alarm bells ringing at full throttle.
So,
with this little bit of background knowledge under our belts, let's
look at what our public health officials and vaccine makers would have
known in advance about coronaviruses and coronavirus vaccines when they
told us back in the early Spring of 2020 that COVID vaccines were the
path back to normality.
From a 2003 study [my emphasis]:
"Until SARS appeared, human coronaviruses were known as the cause of 15–30% of colds...
Colds are generally mild, self-limited infections, and significant
increases in neutralizing antibody titer are found in nasal secretions
and serum after infection. Nevertheless, some unlucky individuals can be reinfected with the same coronavirus soon after recovery and get symptoms again."
In
other words, the coronaviruses involved in colds (there were four human
coronaviruses before SARS, MERS, and COVID) all trigger such a weak
immune response that they do not lead to any long-lasting immunity
whatsoever. And why would they if, for most of us, the threat is so
minimal that the generalists are perfectly capable of neutralizing the
attack.
We also know that immunity against coronaviruses is not
durable in other animals either. As any farmer knows well, cycles of
reinfection with coronaviruses are the rule rather than the exception
among their livestock (for example, coronaviruses are a common cause of
pneumonia and various types of diarrheal diseases like scours, shipping
fever, and winter dysentery in cattle). Annual farm vaccination
schedules are therefore designed accordingly. The lack of long-term
immunity to coronaviruses is well documented in veterinary research among
cattle, poultry, deer, water buffalo, etc. Furthermore, although animal
coronavirus vaccines have been on the market for many years, it is well
known that "none are completely efficacious in animals".
So, like the fading flu vaccine profile I showed you earlier, none of
the animal coronavirus vaccines are capable of providing sterilizing
immunity (none were capable of stopping 100% of infections, without
which you can never achieve herd immunity) and the partial immunity they
offered is well known to fade rather quickly.
What about immunity
to COVID's close cousin, the deadly SARS coronavirus, which had an 11%
case fatality rate during the 2003 outbreak? From a 2007 study: "SARS-specific
antibodies were maintained for an average of 2 years... SARS patients
might be susceptible to reinfection >3 years after initial exposure."
(Bear in mind that, as with all diseases, re-infection does not mean
you are necessarily going to get full-blown SARS; fading immunity after a
natural infection tends to offer at least some level of partial
protection against severe outcomes for a considerable amount of time
after you can already be reinfected and spread it to others - more on
that later.)
And what about MERS, the deadliest coronavirus to
date, which made the jump from camels in 2012 and had a fatality rate of
around 35%? It triggered the broadest immune response (due to its
severity) and also appears to trigger the longest lasting immunity as a
result (> 6yrs)
Thus,
to pretend that there was any chance that herd immunity to COVID would
be anything but short-lived was dishonest at best. For most people,
immunity was always going to fade quickly. Just like what happens after
most other respiratory virus infections. By February 2020, the
epidemiological data showed clearly that for most people COVID was a
mild coronavirus (nowhere near as severe than SARS or MERS), so it was
virtually a certainty that even the immunity from a natural infection
would fade within months, not years. It was also a certainty that
vaccination was therefore, at best, only ever going to provide partial
protection and that this protection would be temporary, lasting on the
order of months. This is a case of false and misleading advertising if
there ever was one.
If I can allow my farming roots to shine
through for a moment, I'd like to explain the implications of what was
known about animal coronaviruses vaccines. Baby calves are often
vaccinated against bovine coronaviral diarrhea shortly after birth if
they are born in the spring mud and slush season, but not if they are
born in midsummer on lush pastures where the risk of infection is lower.
Likewise, bovine coronavirus vaccines are used to protect cattle before
they face stressful conditions during shipping, in a feedlot, or in
winter feed pens. Animal coronavirus vaccines are thus used as tools to
provide a temporary boost in immunity, in very specific
conditions, and only for very specific vulnerable categories of animals.
After everything I've laid out so far in this text, the targeted use of
bovine coronavirus vaccines should surprise no-one. Pretending that our
human coronavirus vaccines would be different was nonsense.
The
only rational reason why the WHO and public health officials would
withhold all that contextual information from the public as they rolled
out lockdowns and held forth vaccines as an exit strategy was to whip
the public into irrational fear in order to be able to make a dishonest
case for mass vaccination when they should have, at most, been focused
on providing focused vaccination of the most vulnerable only. That
deception was the Trojan Horse to introduce endless mass booster shots
as immunity inevitably fades and as new variants replace old ones.
Now, as all the inevitable limitations and problems with these vaccines become apparent (i.e.
fading of vaccine-induced immunity, vaccines proving to only be
partially effective, the rise of new variants, and the vaccinated
population demonstrably catching and spreading the virus ― a.k.a. the
leaky vaccine phenomenon), the surprise that our health authorities are
showing simply isn't credible. As I have shown you, all this was 100% to
be expected. They intentionally weaponized fear and false expectations
to unleash a fraudulent bait-and-switch racket of global proportions.
Immunity on demand, forever.
At
this point you may be wondering, if there is no lasting immunity from
infection or vaccination, then are public health officials right to roll
out booster shots to protect us from severe outcomes even if their
dishonest methods to get us to accept them were unethical? Do we need a
lifetime regimen of booster shots to keep us safe from a beast to which
we cannot develop durable long-term immunity?
The short answer is no.
Contrary
to what you might think, the rapid evolution of RNA respiratory viruses
actually has several important benefits for us as their involuntary
hosts, which protects us without the benefit of broad lifelong immunity.
One of those benefits has to do with the natural evolution of the virus
towards less dangerous variants. The other is the cross-reactive
immunity that comes from frequent re-exposure to closely related
"cousins". I'm going to peel apart both of these topics in order to show
you the remarkable system that nature designed to keep us safe... and
to show you how the policies being forced on us by our public health
authorities are knowingly interfering with this system. They are
creating a dangerous situation that increases our risk to other
respiratory viruses (not just to COVID) and may even push the COVID
virus to evolve to become more dangerous to both the unvaccinated and
the vaccinated. There are growing signs that this nightmare scenario has already begun.
“In this present crisis, government is not the solution to our problem; government is the problem."
- President Ronald Reagan in 1981.
Let's
start with the evolutionary pressures that normally drive viruses
towards becoming less dangerous over time. A virus depends on its host
to spread it. A lively host is more useful than a bedridden or dead one
because a lively host can spread the virus further and will still be
around to catch future mutations. Viruses risk becoming evolutionary
dead ends if they kill or immobilize their hosts. Plagues came, killed,
and then were starved out of existence because their surviving hosts had
all acquired herd immunity. Colds come and go every year because their
hosts are lively, easily spread the viruses around, and never acquire
long-lasting immunity so that last year's hosts can also serve as next
year's hosts ― only those who have weak immune systems have much to
worry about. In other words, under normal conditions, mutations that are
more contagious but less deadly have a survival advantage over less
contagious and more deadly variations.
From the virus' point of
view, the evolutionary golden mean is reached when it can easily infect
as many hosts as possible without reducing their mobility and without
triggering long-term immunity in most of their hosts. That's the ticket
to setting up a sustainable cycle of reinfection, forever. Viruses with
slow genetic drift and highly specialized reproductive strategies, like
polio or measles, can take centuries or longer to become less deadly and
more contagious; some may never reach the relatively harmless status of
a cold or mild flu virus (by harmless I mean harmless to the majority
of the population despite being extremely dangerous to those with weak
or compromised immune systems). But for viruses with fast genetic drift,
like respiratory viruses, even a few months can make a dramatic
difference. Rapid genetic drift is one of the reasons why the Spanish
Flu stopped being a monster disease, but polio and measles haven't. And anyone with training in virology or immunology understands this!
We
often speak of evolutionary pressure as though it forces an organism to
adapt. In reality, a simple organism like a virus is utterly blind to
its environment — all it does is blindly produce genetic copies of
itself. "Evolutionary pressure" is actually just a fancy way of saying
that environmental conditions will determine which of those millions of
copies survives long enough to produce even more copies of itself.
A
human adapts to its environment by altering its behaviour (that's one
type of adaptation). But the behaviour of a single viral particle never
changes. A virus "adapts" over time because some genetic copies with one
set of mutations survive and spread faster than other copies with a
different set of mutations. Adaptation in viruses has to be seen
exclusively through the lens of changes from one generation of virus to
the next based on which mutations have a competitive edge over others.
And that competitive edge will vary depending on the kinds of
environmental conditions a virus encounters.
So, fear mongering about the Delta variant being even more contagious leaves out the fact that this is exactly what
you would expect as a respiratory virus adapts to its new host species.
We would expect new variants to be more contagious but less deadly as
the virus fades to become just like the other 200+ respiratory viruses
that cause common colds and flus.
That's also why the decision to
lock down the healthy population is so sinister. Lockdowns, border
closures, and social distancing rules reduced spread among the healthy
population, thus creating a situation where mutations produced among the
healthy would become sufficiently rare that they might be outnumbered
by mutations circulating among the bedridden. Mutations circulating
among the healthy are, by definition, going to be the least dangerous
mutations since they did not make their hosts sick enough to confine
them to bedrest. That's precisely the variants you want to spread in
order to drown out competition from more dangerous mutations.
A
host stuck in bed with a fever and not out dining with friends is
limited in his ability to infect others compared to a host infected with
a variety that only gives its host a sniffle. Not all bedridden hosts
have caught a more dangerous mutation, but all dangerous mutations will
be found among the bedridden. Thus as time goes by, dangerous mutations
can only compete with less dangerous mutations if the entire population
is limited in its ability to mix and mingle.
As long as the
majority of infections are among the healthy, the more dangerous
variants circulating among some of the bedridden will be outnumbered and
will become evolutionary dead ends. But when public health officials
intentionally restricted spread among the young, strong, and healthy
members of society by imposing lockdowns, they created a set of
evolutionary conditions that risked shifting the competitive
evolutionary advantage from the least dangerous variants to more
dangerous variants. By locking us all up, they risked making the virus
more dangerous over time. Evolution doesn't sit around to wait for you
while you develop a vaccine.
Let me give you a historical example
to demonstrate that this rapid evolution of a virus towards either more
or less dangerous variants isn't mere theory. Small changes to the
environment can lead to very rapid changes in the virus' evolution. The first wave of the 1918 Spanish Flu was not particularly deadly, with mortality rates similar to regular seasonal flu.
However, the second wave was not only much deadlier but, rather
unusually, was particularly deadly to young people rather than just the
old and the weak. Why would the second wave be the deadly one?
And what would cause the virus to evolve so quickly to become both more
deadly and better adapted to preying on young people? At first glance it
would seem to defy all evolutionary logic.
The answer
demonstrates just how sensitive a virus is to small changes in
evolutionary pressure. The Spanish Flu spread in the midst of the
lockdown-mimicking conditions of World War One. During the first wave,
the virus found a huge population of soldiers trapped in the cold damp
conditions of the trenches and a near endless supply of captive
bedridden hosts in overflowing field hospitals. By the Spring of 1918,
up to three-quarters of the entire French military and half of British
troops had been infected. These conditions created two unique
evolutionary pressures. On the one hand, it allowed variants that were
well adapted to young people to emerge. But on the other hand, unlike
normal times, the cramped conditions of trench warfare and field
hospitals allowed dangerous variants that immobilize their hosts to
spread freely with little competition from less dangerous variants that
spread through lively hosts. The trenches and field hospitals became the
virus incubators driving the evolution of variants.
Normally
young people are predominantly exposed to less dangerous mutations
because the healthiest do all the mingling while the bedridden stay
home. But the lockdown conditions of war created conditions that erased
the competitive advantage of less dangerous mutations that don't
immobilize their hosts, leading to the rise of more dangerous
mutations.
Thanks to the end of the war, the lockdown-mimicking
conditions also ended, thereby shifting the competitive advantage back
to less dangerous mutations that could spread freely among the mobile
healthy members of the population. The deadliness of the second wave of
the 1918 Spanish Flu is inextricably linked to the First World War, and
the end of the war is linked to the virus fading into the background of
regular cold and flu season.
Soldiers from Fort Riley, Kansas, ill with Spanish flu at a hospital ward at Camp Funston
It
is therefore highly likely that the 1918 Spanish Flu would never have
been more than a really bad flu season had it not been for the
amplifying effect of lockdown conditions created by a world at war.
It also raises the question, for which I don't have an answer, whether the lockdown strategy during COVID was intentionally used
to reduce spread among the healthy in order to keep the virus from
fading into harmless irrelevancy. I use the word "intentionally" ― and
it's a strong word ― because the deadly second wave of the 1918 Spanish
Flu and its causes are hardly secrets in the medical community. You'd
have to be a completely reckless and utterly incompetent idiot, or a
cynical bastard with an agenda, to impose any strategy that mimics those
virus-amplifying conditions. Yet that's what our health authorities
did. And what they continue to do, while shamelessly hyperventilating
about the risk of "variants" to force us to submit to medical tyranny
based on mandatory vaccines, never-ending booster shots, and vaccine
passports that can turn off access to our normal lives. This is cynicism
at its finest.
The
experience of the 2nd wave of the 1918 Spanish Flu also raises another
question: What kind of evolutionary pressures are being created by using
a leaky vaccine?
A vaccine that provides sterilizing immunity
prevents the vaccinated from being able to catch or transmit the virus.
They become a dead end for the virus. However, as I've already
mentioned, the current crop of COVID vaccines, which are meant to train
the immune system to recognize the S-spike proteins, were not designed
to create sterilizing immunity. By their design, they merely help reduce
the risk of severe outcomes by priming the immune system. The
vaccinated can still catch and spread the virus ― the definition of a
leaky vaccine ― and epidemiological data makes it very clear that this
is now happening all around the world. Thus, both the vaccinated and the
unvaccinated are equally capable of producing new variants. The idea
that the unvaccinated are producing variants while the vaccinated are
not is a boldfaced lie.
Source: "Israel hopes boosters can avert new lockdown as COVID vaccine efficacy fades." August 23rd, 2021, Financial Times,
From
an evolutionary perspective, this is a potentially dangerous scenario.
What has been done by temporarily blunting the risk of hospitalization
or death, but without stopping infection among the vaccinated, is to
create a set of evolutionary conditions where a variant that is
dangerous to the unvaccinated can spread easily among the vaccinated
without making the vaccinated very sick. For lack of a better term,
let's call this a dual-track variant. Thus, because the vaccinated are
not getting bedridden from this dual-track variant, they can continue to
spread it easily, giving it a competitive advantage, even if it is
highly dangerous to the unvaccinated.
Furthermore, since COVID
vaccination only offers temporary short-term protection, as soon as
immunity fades, the vaccinated themselves are also equally at risk of
more severe outcomes. Thus, this creates the evolutionary pressure for
the virus to behave as an increasingly contagious but relatively mild
virus as long as everyone is vaccinated but as a dangerous but also very
contagious virus as soon as temporary immunity wears off. The call for boosters every 6 months is already here. (Update: now it's being revised down to 5 months.)
So, the pandemic really does have the potential to become the Pandemic of the Unvaccinated (the
shameless term coined by public health officials to terrify the
vaccinated into bullying their unvaccinated peers), but reality comes
with a twist because if a dual-track variant does evolve it would be the
unvaccinated (and those whose boosters have expired) who would have
reason to fear the vaccinated, not the other way around as so many
frightened citizens seem to believe. And the end result would be that we
all become permanently dependent on boosters every 6 months, forever.
Hold
on, you might say, the flu vaccine chart shown earlier also never
provided sterilizing immunity. The flu vaccine is notoriously leaky but
hasn't gotten more dangerous, has it? The answer is complicated because
the comparison is less useful than it first appears. As long as the
majority of the population does not get the flu vaccine, more dangerous
variants will face stiff competition from less dangerous ones
circulating among the healthy unvaccinated population (average flu
vaccination rates in most western countries are between 38-41%,
with most other countries around the world doing very little
vaccination against the flu). And since the vaccine is only 40%
effective to begin with and since immunity fades rapidly after the shot,
the flu vaccine doesn't provide much protection to begin with, thus
reducing the chance that separate mutations would circulate among the
vaccinated. And public health frequently gets the strain wrong
(influenza has many strains that are constantly evolving so there is a
lot of guesswork that goes into creating the right vaccine formula each
year). In other words, lack of universal coverage and poor protection
are likely preventing the emergence of a dual-track variant.
Furthermore,
flu vaccination is not evenly distributed across the population. It is
mostly the vulnerable and those who work around them that get it while
children, young adults and other healthy members of society don't get
it. So, even if more deadly variants were to arise in nursing homes or
hospital settings, the high number of healthy unvaccinated visitors to
those facilities would constantly bring less deadly more contagious
variants with them, thereby preventing more dangerous variants from
gaining a competitive edge in nursing home or hospital settings. But if
the leaky flu vaccinations were to be extended to everyone, or if
nursing home populations continue to be kept isolated from the rest of
society during COVID lockdowns, things might begin to look a little
different.
However, what I am warning about is far from
theoretical. There is a very clear example (well known to public health
officials and vaccine developers) from the poultry farming industry
where a universal leaky vaccine pushed a virus to evolve to become extremely deadly to unvaccinated chickens. It is called the Marek Effect.
It began with a leaky vaccine that was rolled out to fight a herpes
virus in industrialized high-density chicken barns. Vaccinated chickens
were protected from severe outcomes but nevertheless continued to catch
and spread the virus, so evolutionary pressure led to the emergence of a
dual-track variant that become the dominant strain of this herpes
virus. It continues to spread among the vaccinated chickens without
killing them but kills up to 80% or more of unvaccinated birds if they
get infected. Thus, a never-ending stream of vaccinations is now
required just to maintain the status quo. I bet the pharmaceutical
industry is smiling at all those drug-dependent chickens though — talk
about having a captive audience!
It's not a certainty that this
will happen with the COVID vaccines, but the longer this fiasco
continues and the higher that vaccination rates rise around the world,
the more likely it becomes that we re-create the conditions for some
kind of Marek effect to develop. A leaky vaccine used sparingly to
protect small pockets of vulnerable individuals is very different than a
leaky vaccine applied to everyone. The rapid change in behaviour of the
1918 Spanish Flu should be a warning to us all that a virus can adapt
very quickly in response to small changes in evolutionary pressure. The
closer we get to universal vaccination, the greater the danger that
leaky vaccines will lead to dual-track variants that become more
dangerous to the unvaccinated.
There is one other danger from
leaky vaccines that is worth mentioning because researchers are already
starting to see the first signs of it, as you can see discussed in this paper published on August 9th, 2021, in the Journal of Infection. It's called antibody-dependent enhancement (ADE).
It happens when a poorly designed vaccine trains antibodies to
recognize a virus as an intruder without being strong enough to
kill/neutralize them. Instead of the virus being neutralized inside the
antibody when the antibody attacks and "swallows" it (antibodies
envelope intruders in order to neutralize them), the virus takes over
the antibody cell that attacked it and uses it as a host to start making
copies of itself. Thus, the attacking antibody opens the door to the
inside of the cell and becomes the virus' unwitting host, thereby
accelerating rather than stopping the infection.
Antibody-dependent enhancement is a well-documented phenomenon in attempts to develop vaccines against the RSV virus, dengue fever, and other coronaviruses.
This is one of the reasons why previous attempts to develop a human
coronavirus vaccine against the SARS virus failed. It kept happening in
animal trials. And many doctors warned from day one that it would happen
with these vaccines as well as new variants gradually emerge that are
sufficiently different from the original variant upon which the vaccine
is based. ADE doesn't show up on the day after vaccination. It emerges
gradually as new variants spread that are different from previous
variants.
Quote from the aforementioned study:
ADE
may be a concern for people receiving vaccines based on the original
Wuhan strain spike sequence (either mRNA or viral vectors). Under these
circumstances, second generation vaccines with spike protein
formulations lacking structurally-conserved ADE-related epitopes should
be considered.
In other words, your previous
vaccination protects you only until new variants arise, then the
training that your previous vaccination gave your immune system becomes a
liability as your immune system switches from protecting you to
increasing your risk from the disease. Your only way to protect yourself
is to dutifully get your next "updated" booster shot to protect you for
next few short months. You become a permanent drug dependent vaccine
customer. And you better hope next year's formulation doesn't get it
wrong. And you better hope that updates can keep you safe indefinitely
because there's also the risk that updates will get less effective as
the bad training from previous boosters begins to add up.
It puts a whole new spin on "trust the scientists." Your life will literally be at their mercy.
I bet the pharmaceutical industry will be smiling at all those drug-dependent chickens loyal
customers though — talk about having a captive audience! And what a
sweet deal - vaccine makers have been granted an exemption from
liability and, if it goes wrong, they are the go-to guy to solve it...
with more boosters.
And with every booster, you'll get to play
Russian Roulette all over again with side effects: death, autoimmune
diseases, reactivation of dormant viruses, neurological damage, blood
clotting, and more. Here's where the reported side effects on the US
VAERS system stand at the time of writing (August 28th, 2021).
OpenVaers Search, August 28th, 2021
Leaky
vaccines are playing with fire. All vaccine makers and public health
authorities were aware of the potential for ADE with the development of a
coronavirus vaccine. Yet they pushed for mass vaccination, from day
one, without completing the long-term trials that are meant to rule out
this kind of risk. They knowingly gambled with your future in their
eagerness to get you onto your regimen of never-ending boosters and
vaccine passports. Why not, if more boosters are the solution if
something going wrong. They can always blame it on the "variants". The
media won't challenge them - not with billions of vaccine advertising
dollars floating around.
And
now we come to the second way in which our immune systems benefit from
the rapid evolution of RNA respiratory viruses and to the sinister way
in which public health policy is interfering with that system.
The
once deadly 1918 Spanish Flu is still with us today; now it is part of
the smorgasbord of viruses that cause colds and flus every winter
precisely because subsequent variants evolved to be less deadly. As
unpleasant as flu season is, for most of us it is not lethal unless we
have weak or compromised immune systems. But each subsequent exposure teaches our immune system how to keep up with its gradual evolution over time.
In
other words, each year's fresh exposure to the latest strain of cold or
flu virus functions as a sort of antivirus security update to partially
prepare you for the next one. Fading immunity and changing mutations
means you'll never be 100% immune to the next one, but as long as
updates are frequent enough, you'll also never have 0% immunity. There
will always be enough carry-over to protect you from the most serious
outcomes unless you are unfortunate enough to have a weak immune system.
That is why it is called cross-reactive immunity.
A
broad smorgasbord of viruses cruising around during cold and flu season
makes it less likely that we will die or get seriously ill when exposed
to some new "variant" from London, India, or Brazil, or if we are
exposed to a new "cousin", like COVID, which crawls out of some bat cave
or wet market or escapes from some lab in Wuhan.
Partial cross-reactive immunity requires periodic re-exposure. Modified from Nature, 4704, September 17th, 2020.
But
when we think about it for a moment, what was once dangerous when it
was new soon becomes our most important ally for the future to protect
us from the next dangerous new thing. As long as we are re-exposed
frequently, before immunity fades to zero, cross-reactive immunity is
the only realistic evolutionary strategy that humans have to protect us
from the next viral variant or viral cousin of these fast-mutating
respiratory viruses.
With sufficient leftover cross-reactive
immunity from your last exposure, exposure to the latest variant of a
virus may simply result in your immune system getting updated without
you even noticing a single thing. That's what it means to get an
"asymptomatic" infection. Before we started tormenting the healthy with
never-ending PCR tests to make us aware of all these "asymptomatic
infections", we were constantly getting lots of these "antivirus
security updates" each time we encountered one of the more than 200
respiratory viruses circulating among us, often without even noticing
the "infection".
Many of these encounters are asymptomatic
because our immune systems are able to neutralize them without even
ruffling enough layers of our defenses to trigger any symptoms. Almost
everyone gets a few immune system updates to the viruses that cause
common colds, every single year, yet only a small percentage will ever
get very sick. The rest may barely get a runny nose, or nothing symptoms
at all.
Mass PCR testing during COVID created a massive
freak-out over every single asymptomatic COVID update when we should
have only been focused on those people who come down with severe
symptomatic disease. There was never any justifiable reason to roll out
PCR tests to asymptomatic citizens other than to heighten fear in the
population in order to make them receptive to mass vaccination.
So,
in a sense, those 201 respiratory viruses that cause our colds and flus
are not just an inconvenience, they are nature's solution to software
updates ― even though they are dangerous to those with weak immune
systems, for the rest of us our immune systems depend on them
to give us partial protection against new strains that emerge through
mutation or when new strains jump across species boundaries. Getting rid
of those already circulating in society would make us more vulnerable to new variants that emerge. Adding another 200 will make us even safer once we get our first contact behind us.
Eradicating a relatively benign respiratory virus is therefore not a
desirable goal. But making it fade into the background is a desirable
public health goal so that what was once dangerous can now keep
protecting us against the next one through cross-reactive immunity.
Focused protection for the vulnerable, not lockdowns, was always the
only realistic public health response to this respiratory virus, unless
someone wanted to seize the opportunity as a way to rope the public into
mass vaccinations.
Nature evolved this fascinating strategy of
self-updating immunological countermeasures by continually testing us
with mild versions of previous closely related respiratory viruses. Our
immune system is therefore somewhat similar to an Olympic weightlifter
whose muscles not only stay strong but get even stronger by routinely
putting his muscles under a little bit of stress. Our immune system
functions the same way ― it must be continually stress-tested with mild
challenges to these fast-mutating viruses in order to develop the robust
arsenal of defenses to keep us safe. It is a concept called anti-fragility, which was described in detail by Nassim Taleb in his ground-breaking book, Antifragile: Things That Gain from Disorder #Commissions Earned. Once you understand this concept, your fear of "variants" will rapidly dissolve.
The
eradication of these fast-mutating respiratory viruses is therefore not
just unachievable, it would actually be dangerous if we succeeded
because it would eliminate the security updates that we need to protect
us against new variants that crawl out of bat caves or jump species
boundaries. This year's runny nose is your protection against COVID-23.
Your cross-reactive immunity to last years annoying flu might just save
your life if something truly dangerous arrives, as long as it is at
least somewhat related to what your immune system has seen before. COVID
could easily have turned out to be as dangerous to us as the Spanish
Flu if it hadn't been for the saving grace of cross-reactive immunity. As this study shows,
up to 90-99% of us already had some level of protection to COVID thanks
to partial cross-reactive immunity gained from exposure to other
coronaviruses. The high percentage of infections that turn out to be
asymptomatic bears that out.
Someone needs to remind Bill Gates,
his fawning public health bootlickers, and the pharmaceutical companies
that whisper sweet-nothings in his ear that in the natural world of
respiratory viruses, most of us don't need a regimen of never-ending
booster shots to keep us safe from COVID variants ― we already have a
perfectly functioning system to keep bringing us new updates.
Respiratory viruses are a completely different beast than smallpox,
polio, or measles; and pretending otherwise is not just silly, it's
criminal because anyone with a background in immunology knows better.
But it's a fantastic and very profitably way to scare a wide-eyed
population into accepting never-ending booster shots as a replacement
for the natural antivirus updates that we normally get from hugs and
handshakes. Protect the vulnerable. Stop preying on the rest of us.
A truly novel virus
affects everyone because no-one has pre-existing cross-reactive partial
immunity to it. That's why the diseases that accompanied Christopher
Columbus to the Americas killed up to 95% of North and South America's
indigenous populations (see Guns, Germs, and Steel, by Jared Diamond #Commissions
Earned). To them, these diseases were novel because they had no
previous exposure to them and therefore lacked the antivirus security
updates acquired through pre-existing infections. They would have
benefited greatly from access to a vaccine prior to first contact.
Thankfully, COVID-19 was not that
kind of virus. Yet the media and public health officials shamelessly
provoked fear that it was by using the scientifically accurate term novel to
describe it, knowing full well that all scientists would understand
this to mean a newly emergent strain while the general public would jump
to the conclusion that this was an entirely new virus (also called a novel virus
by scientists), like when tuberculosis or influenza accompanied
Columbus to the Americas. This was a grotesque example of public health
officials misusing scientific terminology, knowing full well that the
public would misunderstand the term novel according to how we use the word in everyday language and not according to how the scientific community uses it.
That
little game successfully sparked a wave of fear that is so strong that
not only is everyone desperate for a leaky jab to lead them to safety,
they are so scared that they won't rest until all their friends,
neighbors, and family members get one too, even if it requires extreme
levels of coercion to get the job done. Canada has even recently gone as
far as making vaccination mandatory for all federal employees,
employees of Crown Corporations, employees of federally-regulated
companies (i.e. utilities) and for all travellers on commercial airlines
and trains (CBC, August 13th, 2021) !
Despite the scary numbers put out by the Chinese government in the early days of the pandemic, the outbreak on the Diamond Princess cruise
ship served as an inadvertent petri-dish to study the COVID virus.
Thanks to that example, by the end of February 2020, we knew that COVID
was not some monster virus like the 1918 Spanish Flu but was simply
another coronavirus strain that was closely related to previous
coronaviruses and that most of us already carried some level of
cross-reactive immunity to protect us.
How do we know that? The virus circulated freely onboard the ship, yet age corrected lethality remained between 0.025% and 0.625% (that's
on the order of a bad flu season and nothing at all like the fatality
rate of the 1918 Spanish Flu, which was between 2% and 10%). Only 26% of the passengers tested positive for the virus and of those that tested positive 48% remained completely symptom free despite the advanced age of most of these passengers!
Diamond Princess Cruise Ship, Alpsdake, CC BY-SA 4.0.
The Diamond Princess didn't
turn into the floating morgue of bygone eras when ships carrying a
disease were forced into quarantine. That should have been the first
clue that this virus was anything but novel in the colloquial
understanding of the term. Like most cold and flu viruses, only those
with weak immune systems were in danger while everyone else got off with
little or no symptoms. That is simply not how a truly novel
virus behaves when it encounters a population without any pre-existing
cross-reactive immunity. The only plausible explanation for that lack of
deadliness (deadly for some, annoying for some, and asymptomatic for
most others) is that most people already have sufficient pre-existing
cross-reactive immunity from exposure to other coronaviruses.
Research subsequently confirmed what the Diamond Princess outbreak revealed. Cross-reactive immunity. As I mentioned before, studies like this one demonstrated that up to 90 - 99% of us already have some residual level of partial protection to COVID. And we also subsequently found out that most people who were exposed to the deadly SARS virus in 2003 have little to fear from COVID, again because of cross-reactive immunity. COVID was never a mortal threat to most of us.
The important thing to remember is that the Diamond Princess data was already publicly available since the end of February of 2020. Operation Warp Speed, the
vaccine development initiative approved by President Trump, was
nevertheless announced on April 29th, 2020. Thus, our health authorities
knowingly and opportunistically recommended lockdowns and promoted
vaccines as an exit strategy after it was already clear that the majority of us had some kind of protection through cross-reactive immunity. The Diamond Princess example
provided the unequivocal proof that the only people who might benefit
from a vaccine, even if it worked as advertised, were the small number
of extremely vulnerable members of society with weak immune systems.
Likewise, lockdowns should have been recommended only for nursing home residents (on a strictly voluntary basis to protect their human rights) while the pandemic surged through the rest of us.
The only plausible explanation for why our international health authorities ignored the example of the Diamond Princess is
if they wanted to stoke fear among the public and if they wanted to
bamboozle credible politicians in order to opportunistically achieve
some other public health agenda. They pushed vaccination on everyone
knowing full well that most people don't need it and that protection
would fade quickly even if the vaccines had been 100% effective, which
they also knew was not going to be the case either. And yet they
continue to push these vaccines using the same deceitful tactics even
today. Water does not run uphill.
“We know they are lying,
they know they are lying,
they know we know they are lying,
we know they know we know they are lying,
but they are still lying.”
- Attributed to Aleksandr Isayevich Solzhenitsyn
Just
like during other cold and flu seasons, the vulnerable to COVID are
overwhelmingly those with compromised immune systems: those whose immune
systems are shutting down as they approach death from old age and those
whose immune systems are compromised due to severe pre-existing
conditions that reduce immune function.
For everyone else with a
strong immune system and cross-reactive immunity, we have little to fear
from the virus and its never-ending stream of mutations unless our immune systems are temporarily suppressed through illness, environmental conditions, or nutritional deficiencies.
Your
mother's warnings about putting on a sweater, hat, and dry socks,
tucking in your shirt to cover your kidneys, and not playing in puddles
were not about preventing infection by a cold or flu, it was about preventing symptomatic infection. Research has demonstrated that getting chilled can temporarily suppress your immune system.
Thus, getting chilled increases the chance that an infection leads to
symptomatic disease rather than merely updating your immune system
through an asymptomatic infection. Your sweater won't prevent you from
catching an infection. But it might prevent that infection from becoming
a symptomatic disease. It could be the difference between experiencing
nothing and ending up in bed with a fever.
In the same way,
topping up on vitamin C and D, eating properly, getting enough rest,
getting hugs from loved ones, adopting a positive attitude in life, and
smiling when you see a rainbow are all strategies that help keep your
immune system strong. They don't prevent infection, but they might
reduce your risk of a bad outcome.
Ask
the staff in a nursing home what happens to their patients when any of
these important ingredients is missing ― vitamin and nutrient
deficiencies, poor sleep, loneliness, and depression lay out the welcome
mat for the Grim Reaper. A temporarily suppressed immune system cannot
mount an adequate immune response even when we do have cross-reactive
immunity.
Our public health authorities also all know this. This
is not a mystery. Yet, instead of promoting these strategies as ways in
which people could reduce their risk to severe outcomes, they have
systematically downplayed, ignored, or labeled these strategies as "fake news". Maximize the risk of death. Then promote the vaccine as the exclusive path to safety. Criminal.
You
cannot control other people forever to avoid getting exposed to a
respiratory virus. COVID Zero is an authoritarian fantasy. But you can
control your food, your sleep, and your attitude so that your immune
system can mount the strongest attack it can muster. The odds are that
you already have all the cross-reactive immunity you need to survive
this virus without a hitch. Look inwards to find freedom from fear. Take
good care of yourself. Go play in the sun with your friends. And listen
to your mother —tuck in your shirt!
As
is so often the case when politicians try to run our lives for us, the
government response to COVID is not just wrong, it is actually making us
more vulnerable, both to COVID and to other respiratory viruses.
Depriving nursing home patients of their loved ones, locking them in
isolation, locking people in their homes, shutting down gyms, driving us
into depression, and paralysing us with fear and uncertainty ensures
that our immune systems will be working at suboptimal levels. Broken
marriages, children deprived of social contacts, insomnia, the
remarkable surge in obesity that occurred during COVID, and so many
other consequences of these ill begotten strategies all have a toll on
our ability to mount a strong immune response when we are inevitably
exposed to any respiratory viruses.
Equally devastating is that,
by disrupting our normal social contacts, we have reduced how much
training our immune system is getting through repeated exposure to other
respiratory viruses. A computer that stops getting security updates
becomes increasingly vulnerable to future versions of viruses. The same
goes for our immune system. COVID is not the only risk. Remember, there
are more than 200 other respiratory viruses that are also circulating.
They may not be getting much attention and may be temporarily starved
for hosts while we are cooped up at home, but they haven't gone away.
They are waiting. And when they find us, they find hosts whose antivirus
security updates are out of date.
In other words, by breaking
our ability to socialize with our peers, what was once relatively
harmless is becoming more dangerous to us because our immune systems are
out of practice. This isn't some theoretical risk. We're already
beginning to see the fallout from that lack of updates, with deadly
consequences.
For example, New Zealand was praised
internationally for adopting a COVID-Zero policy and for the low COVID
cases that resulted. But the lockdowns, social distancing measures, and
border closures also had another effect ― there was a 99.9% reduction in flu cases and a 98% reduction in cases of the RSV virus. Sounds good, right? Not so fast...
Systems
that depend on constant challenges to become antifragile will become
fragile if those challenges stop happening. A tree that grows up
sheltered from the wind will break when it is exposed to the storm.
Now New Zealand's myopic focus on COVID as the one and only risk is coming home to roost. Its hospitals are overflowing with children.
But they're not being hospitalized by COVID. They are falling ill with
RSV virus because of the "immunity debt" that built up from not being
continually exposed to all the respiratory viruses that make up normal
life. These children are, quite literally, the next wave of victims of
COVID-Zero. Being cut off from normal life has left them fragile.
Instead of praise, it now is becoming apparent that New Zealand's
authoritarian strongwoman, Jacinda Ardern, and her public health
advisors ought to be standing trial for gross negligence for ignoring
the long-established research about how our immune systems depend on continual exposure to respiratory viruses in order to stay healthy.
Source: The Guardian, July 8th, 2021.
As
long as our social contacts are restricted, we are all becoming
increasing vulnerable to all these other respiratory viruses because of
the "immunity debt" that has built up during lockdowns and social
distancing rules. It turns out that handshakes and hugs are not just
good for the soul. Our public health officials have blood on their hands
for denying us our normal lives.
This heightened risk to other
viruses isn't an unexpected outcome; there were plenty of doctors who
warned about precisely this risk as lockdowns were being imposed. For
example, Dr. Dan Erickson and Dr Artin Massihi warned
about this phenomenon back in May of 2020. YouTube censored their
video. Yet they were citing long-established science that was
uncontested until society collectively lost its mind in 2020.
Introducing
Immunity as a Service – A Subscription-Based Business Model for the
Pharmaceutical Industry (It was always about the money!)
As
you can see from everything I have laid out in this essay, this
misbegotten vaccine-enabled fever dream was never a realistic solution
to stop COVID. At best, if the vaccines worked as advertised, all they
could ever have been was one tool among many to provide the vulnerable
with focused protection while the rest of us went about our normal
lives, largely unaffected by our periodic antivirus security updates
through exposure to the natural virus.
COVID-Zero in all its variations was a fantasy.
But it was not an accidental fantasy.
Water does not run uphill.
Every
single public health official in the world has the education to know
that what they have been promoting, from day one, is gibberish. What I
have laid out in this essay is pretty basic virology and immunology
knowledge. Which raises a rather alarming question: how can any
virologist, immunologist, vaccine maker, or public health official
knowingly promote this lie?
Why is there such a blind obsession
with getting us all to take a vaccine that most people do not need and
that can never provide long-lasting herd immunity?
It's no mystery
why pea-brained politicians might fall for this fantasy; they are only
as good as the advisors they listen to. And politicians are shameless
opportunists, so it is not surprising that they are now exploiting the
situation to increase their powers and to harness this emerging
command-and-control economy in pursuit of their own ideological goals —
redistribution, carbon net zero, social credit score systems, you name
it. In this Orwellian world, if you have a podium and a utopian dream,
the world is your oyster, at least as long as the band keeps playing and
the pitchforks can be kept off the streets.
"You
never let a serious crisis go to waste. And what I mean by that it's an
opportunity to do things you think you could not do before."
- Rahm Emanuel
"I really believe COVID has created a window of political opportunity..."
- Chrystia Freeland, Deputy Prime Minister of Canada
But
our public health officials and international health organizations are
trained to know better. Yet they nevertheless set this nightmare in
motion in violation of all their own long-established pandemic planning
guidelines. They know eradication is impossible. They know most of us already have cross-reactive immunity. They know most of us are healthy enough so that our immune systems will protect us against severe outcomes from this virus. They know about the negative consequences imposed on our immune systems when we are prevented from living normal lives. They know they
are increasing our risk to other viruses by preventing us from
socializing. It's their job to know. And, as I have demonstrated, they
have known since day one.
But what if a shameless pharmaceutical
industry could manipulate public health policies by capturing
politicians, policymakers, and public health agencies through generous
donations? What if the boundaries between public health agencies,
international public health organizations, and pharmaceutical companies
have become blurred to such a degree that each benefits from reinforcing
one another's best interests? What if they have all come to believe
that vaccines against respiratory viruses are the holy grail of public
health (and of generous funding), even if they have to play fast and
loose with the truth to get humanity to accept them and even if they
have to do a little evil to achieve some imagined future "greater good"?
What
if the revolving door between pharmaceutical companies, public health,
and international health organizations has created a kind of blind
groupthink within this holy trinity? What if anyone caught up in that
system is forced to bite their tongue because to speak out is a
deathblow to their career? What if many of those caught up in the
system genuinely believe the lies, despite a lifetime of
training that should tell them otherwise? The powerful effect of
groupthink, demonstrated by the Ash Conformity Experiments,
can make people blind to what is staring them in the face. Even the
medieval kings knew they needed a court jester to prevent the king from
growing a big head. But what if, in the hallowed halls of this holy
trinity, all the court jesters have long since been purged or cowed into
silence?
"It's dangerous to be right when the government is wrong."
- Voltaire
A
quote that best sums up the thinking inside many of our public health
institutions comes from Peter Daszak, head of EcoHealth Alliance, a
non-profit non-governmental organization that works closely with public
health agencies like the National Institutes of Health (NIH) and
intergovernmental organizations like the WHO (published in a 2016 report by the National Academy of Sciences):
"Daszak
reiterated that, until an infectious disease crisis is very real,
present, and at an emergency threshold, it is often largely ignored. To sustain the funding base beyond the crisis, he said, we need to increase public understanding of the need for MCMs [medical counter measures] such as a pan-influenza or pan-coronavirus vaccine. A
key driver is the media, and the economics follow the hype. We need to
use that hype to our advantage to get to the real issues. Investors will
respond if they see profit at the end of process, Daszak stated." [Emphasis mine]
In
the presence of so much conflict of interest, in the absence of the
checks and balances provided by individual rights, in the censorious
atmosphere of cancel culture that has infected all our public
institutions, and with so many institutional donors (private and
governmental alike) being enamored with social-engineering projects and
blinded by their own arrogance, it would perhaps be more surprising if
this vaccine-fueled hysteria hadn't happened.
In view of
the circumstances, what happened almost seems inevitable. To the eyes
of profit-hungry pharmaceuticals and funding-hungry national and
international public health institutions, this virus must look like
manna from heaven. They must feel like a fox that has been invited into
the henhouse by ripe chickens that are begging to be plucked.
History
never repeats itself, but it does often rhyme. What has emerged during
COVID is simply a bigger, better, bolder replay of what happened during
the 2009 swine flu hysteria. I'd like to share a few quotes with you -
and keep in mind that these are about the 2009 Swine Flu scandal, not
COVID:
From a 2010 article entitled: European Parliament to Investigate WHO and "Pandemic" Scandal [Emphasis mine]:
"In his official statement to the Committee, Wodarg criticized the influence of the pharma industry on scientists and officials of [the] WHO, stating that it has led to the situation where "unnecessarily millions of healthy people are exposed to the risk of poorly tested vaccines," and that, for a flu strain that is "vastly less harmful" than all previous flu epidemics."
"For the first time, the WHO criteria for a pandemic was changed in April 2009 as
the first Mexico cases were reported, to make not the actual risk of a
disease but the number of cases of the disease [the] basis to declare
"Pandemic." By classifying the swine flu as [a] pandemic,
nations were compelled to implement pandemic plans and also t[o]
purchase swine flu vaccines."
And here are a series of even more revealing quotes from a 2010 report published by Der Spiegel called: Reconstruction of a Mass Hysteria — The Swine Flu Panic of 2009:
"Researchers
in more than 130 laboratories in 102 countries are constantly on the
lookout for new flu pathogens. Entire careers and institutions, and a
lot of money, depend on the outcomes of their work. "Sometimes you get the feeling that there is a whole industry almost waiting for a pandemic to occur,"
says flu expert Tom Jefferson, from an international health nonprofit
called the Cochrane Collaboration. "And all it took was one of these
influenza viruses to mutate to start the machine grinding."
"Does this mean that a very mild course of the pandemic was not even considered from the start? At any rate, efforts
to downplay the risks were unwelcome, and the WHO made it clear that it
preferred to base its decisions on a worst-case scenario. "We wanted to overestimate rather than underestimate the situation," says Fukuda [Keiji Fukuda was the Assistant Director-General for Health, Security and Environment for the WHO at that time]."
"The media also did its part in stoking fears.
SPIEGEL, for example, had reported at length on the avian flu. Now it
devoted a cover story to the new "global virus," a story filled with
concerns that the swine flu pathogen could mutate into a horrific
virus."
"The pharmaceutical industry was particularly adept at keeping this vision alive."
"We expected a real pandemic, and we thought that it had to happen. There was no one who suggested re-thinking our approach."
"the
vast majority of experts on epidemics automatically associate the term
"pandemic" with truly aggressive viruses. On the WHO Web site, the
answer to the question "What is a pandemic?" included mention of "an
enormous number of deaths and cases of the disease" -- until May 4,
2009. That was when a CNN reporter pointed out the discrepancy between
this description and the generally mild course of the swine flu. The language was promptly removed."
"'Sometimes
some of us think that WHO stands for World Hysteria Organization,' says
Richard Schabas, the former chief medical officer for Canada's Ontario
Province."
"A party with strong connections in
Geneva had a strong interest in phase 6 being declared as quickly as
possible: the pharmaceutical industry."
"Meanwhile, a debate had erupted over whether Germany had chosen the wrong vaccine, Pandemrix [it was later found to have caused narcolepsy in some patients, which is an autoimmune disease]. It contained a new type of agent designed to boost its effectiveness, known as an adjuvant, which had never undergone large-scale human trials in connection with the swine flu antigen. Were millions of people about to receive a vaccine that had hardly been tested?"
"But the
contracts for Pandemrix had been signed in 2007, and they came into
effect automatically when the WHO decided to declare phase 6."
"The ministers felt pressured from all sides. On the one hand, the media were stoking fears of the virus. The German tabloid newspaper Bild, in particular, was printing new tales of horror almost daily. On the other hand, the pharmaceutical companies were upping the pressure and constantly setting new ultimatums."
"Oct.
9, 2009: Wolf-Dieter Ludwig, an oncologist and chairman of the Drug
Commission of the German Medical Association , says: 'The health
authorities have fallen for a campaign by the pharmaceutical companies,
which were plainly using a supposed threat to make money.'"
"Oct.
21, 2009: A BILD newspaper headline, printed in toxic yellow, warns:
"Swine Flu Professor Fears 35,000 Dead in Germany !" The professor's
name is Adolf Windorfer, and when pressed, he admits that he has received payments from the industry, including GSK and Novartis. Next to the BILD headline is an ad for the German Association of Pharmaceutical Companies."
"According to Wodarg, the
WHO's classification of the swine flu as a pandemic have earned the
pharmaceutical companies $18 billion in additional revenues. Annual sales of Tamiflu alone have jumped 435 percent, to €2.2 billion."
Rinse and repeat in 2020-2021.
What
if, upon recognizing the emergence of a new pandemic, those in the know
opportunistically made vaccines the endgame? What if all the vaccine
injuries recorded on VAERS and all the risks they are taking with our
lives are simply collateral damage - a calculated investment risk - in
order to turn their dream of subscription-based "immunity as a service"
into reality.
In the words of Bill Gates, “we kind of caught mRNA half way to prime time.” Maybe
we should believe him — and gape in awe at the recklessness and
contempt they have shown for their fellow citizens in order to
capitalize on this "window of opportunity". Carpe diem (seize the day).
Don't sweat the small stuff. Keep your eye on the ball... and on the
year-end bonuses.
What if COVID-Zero, in all its variations, was
merely a strategy to herd us together so we obediently line up for an
endless string of booster shots as a trade-off for access to our lives?
In
other words, what if someone could bamboozle our leaders into believing
that the only way back to a normal life is for vaccines to replace the role that hugs and handshakes used to play in order to update us with the latest antivirus security updates?
What
if, by depriving us of normal life, those who stand to gain from
vaccines can forever cement themselves at the center of society by
providing an artificial replacement for what our immune systems used to
do to protect us against common respiratory viruses back when we were
still allowed to live normal lives?
The headlines tell the story:
"Pfizer CEO says third Covid vaccine dose likely needed within 12 months." (CNBC, April 15th, 2021)
"Variants could be named after star constellations when Greek alphabet runs out, says WHO Covid chief." (The Telegraph, August 7th, 2021)
"Fauci warns Americans may face having booster shots indefinitely" (Daily Mail, August 13th, 2021, and Dr. Fauci in his own words on YouTube on August 12th, 2021)
"Biden OKs booster shots 5 months after 2nd dose" (Boston Globe, August 27th, 2021)
What
if the fast mutation of RNA viruses ensures that no vaccine will ever
be fully effective at providing lasting immunity, thus creating the
illusion that we are permanently in need of vaccine boosters?
What if politicians could be convinced to make vaccination mandatory in order to prevent potential customers from opting out?
What
if, by relying on lockdowns during the winter season, our vulnerability
to other viruses increased, which could then be used to rationalize
expanding the jab, via mission creep, to simultaneously vaccinate us
against RSV, influenza, other coronaviruses, the common cold, and so on,
despite knowing full well that the protection that these vaccines offer
against respiratory viruses is only temporary?
And what other
social engineering goals can be rolled into your annual booster shot in
the future once you are permanently bound to these annual jabs and
vaccine passports? In an atmosphere of hysteria, it's a system ripe for
abuse by opportunists, ideologues, power hungry totalitarians, and
Malthusian social engineers. The snowball doesn't have to grow by
design. Mission creep happens all on its own once Pandora's Box is
opened to coerced vaccinations and conditional rights. The road to Hell
is frequently paved by good intentions... and hysteria.
So, what
if COVID-Zero and the vaccine exit strategy is merely the global
state-sanctioned equivalent of a drug dealer creating dependency among
its customers to keep pushing more drugs?
What if it was all just a way of convincing society of the need for subscription-based "immunity as a service"?
The subscription-based business model (or some version of it) is all
the rage these days in the corporate world to create loyal captive
audiences that generate reliable money streams, forever. Subscriptions
are not just for your cable TV and gym membership anymore. Everything
has been redesignated as a "consumable".
Netflix did it with movies.
Spotify did it with music.
Microsoft did it with its Office suite.
Adobe did it with Photoshop editing suite.
The smartphone industry did it with phones that need to be replaced every 3 to 5 years.
The gaming industry did it with video games.
Amazon is doing it with books (i.e. Kindle Unlimited).
The food industry is doing it with meal delivery services (i.e. Hello Fresh).
Uber is doing it with subscription-based ride sharing.
Coursera is doing it with online education.
Duolingo and Rosetta Stone are doing it with language learning.
Zoom is doing it with online meetings.
Monsanto
and its peers did it to farmers with patented seed technology, which
cannot legally be replanted, and is lobbying to try to legalize the use
of terminator seed technology (GMO seeds that are sterile in the second
generation to prevent replanting).
The healthcare industry is doing it with concierge medical services, fitness tracking apps (Fitbit), sleep-tracking apps, and meditation apps.
The
investment industry is doing it with farmland, with investors owning
the land and leasing it back to farmers in a kind of modern revival of
the sharecropping system. (Bill Gates is the largest farmland owner in the USA - are you surprised?)
Blackrock and other investment firms are currently trying to do it with homes to create a permanent class of renters.
And
public health authorities and vaccine makers have been trying to do it
with flu vaccines for years, but we've been stubbornly uncooperative.
Not anymore.
Remember when the World Economic Forum predicted in 2016 that by 2030 all products would become services?
And remember their infamous video in which they predicted that "You
will own nothing. And you will be happy."? Well, the future is here.
This is what it looks like. The subscription-based economy. And
apparently it now also includes your immune system in a trade-off for
access to your life.
Original video on Facebook, World Economic Forum, December 9th, 2016.
Let's revisit the Peter Daszak quote from earlier. A second read allows the message to really hit home:
"Daszak
reiterated that, until an infectious disease crisis is very real,
present, and at an emergency threshold, it is often largely ignored. To sustain the funding base beyond the crisis, he said, we need to increase public understanding of the need for MCMs [medical counter measures] such as a pan-influenza or pan-coronavirus vaccine. A
key driver is the media, and the economics follow the hype. We need to
use that hype to our advantage to get to the real issues. Investors will
respond if they see profit at the end of process, Daszak stated."
Isn't
it ironic that he didn't even care which vaccine was pushed? Influenza
or coronavirus, it made no difference. It was always about funding. It
was always about the money. It always was. It always is.
The holy
trinity of pharmaceutical companies, public health, and international
health organizations, all egging each other on in their hunger for a
reliable flow of cash: shareholder profits, larger budgets, and
governmental donations. Their interests are perfectly aligned and the
lines between them are blurred to such a degree that each benefits from
reinforcing one another's best interests.
And why would politicians and media bow to the holy trinity?
Big Pharma spent an average of US$4.7 billion per year between 1999 and 2018 on lobbying and campaign contributions, just in the USA!
Big Pharma also shells out $US20 billion each year to schmooze doctors and another US$6 billion on drug ads,
just in the USA! So, it's no surprise why legacy media and Big Tech are
tripping over themselves not to ruffle the party line — they live and
die by the almighty advertising dollar. Never bite the hand that feeds
you.
So, they are all dancing to the same tune while your pocket
gets picked and your arm gets pricked, and everyone wins... except you
and me. We are the cow that gets milked. We are the serfs that fund
their largesse in this neo-feudal society where a few big boys own the
assets and everyone else is beholden to those above them in the
hierarchy for access to, well, everything — land, resources, rights,
individual autonomy, and even immune systems. My body, their choice.
What
if, in an atmosphere of runaway hysteria, a police state founded on
medical tyranny is creating itself, fueled by a toxic brew of
self-serving opportunists who have seized the moment to superimpose
their own goals on a fortuitous virus, until one day you wake up to find
yourself chained and milked, like a cow in a dairy barn, under the
absolute custody of a modern-day Louis the Fourteenth and his royal
court full of drug pushers, ideologues, and militant devotees? The
modern face of feudalism, updated for the 21st century. Neo-feudalism,
enforced by a mandatory subscription-based "immunity as a service".
And
what if a society that has lost its principles, a society that is eager
to hand over individual responsibility to "experts," a society that is
held hostage to cancel culture mobs, a society that no longer has
transparency into the decisions made by its experts, a society led by a
censorious political class full of immoral opportunists, a society that
has fallen so in love with big government that red tape and cronyism
have completely erased the self-limiting checks and balances of a free
and open society, and a society that has elevated safety to a new sort
of religious cult is a society that has no immunity to protect itself
from predators who treat us like cattle?
No period in history has
ever lacked in snake-oil salesmen, ideologues, and social engineers
eager to take society for a ride. Most of the time, they are ignored.
So, what if the only real mystery is why society has grown so willing to
accept the collar and yoke?
What if all this really is just as simple as that?
Now
we know we've been played, how we've been played, and why we've been
played. Again. Just like during the 2009 Swine Flu con. Only bigger,
bolder, and better. They learned from their mistakes. We didn't.
But
now that you see the con, you can't unsee it. And now that you
understand the threat and how the game is being played, there is a
weight that comes off your shoulders.
When you know there's a
threat, but you don't know exactly what it is, every movement in the
grass might be a tiger or a snake or a scorpion. It's paralysing and
exhausting to defend yourself against an invisible unknown and they have
used that fear masterfully against us to keep us frozen. But once you
spot the tiger in the grass, you know where to direct your focus, your
feet become unglued, your voice becomes bold, and you regain the clarity
of thought to defend yourself.
The con is clear. It's time to
focus all our might on stopping this runaway train before it takes us
over the cliff into a police state of no return. Stand up. Speak out.
Refuse to play along. Stopping this requires millions of voices with the
courage to say NO — at work, at home, at school, at church, and out on
the street.
"Nonviolent direct action seeks to
create such a crisis & foster such a tension that a community which
has constantly refused to negotiate is forced to confront the issue. It
seeks so to dramatize the issue that it can no longer be ignored." — Martin Luther King Jr.
Compliance is the glue that holds tyranny together. Non-compliance breaks it apart. One
person alone cannot stop this. But if millions find the courage to
raise their voices and the courage to refuse to participate in the
system on these tyrannical medical terms, it will throw the system into
such a crisis and create such a tension that the community will be
forced to confront the issue. Without enough truckers, no-one eats.
Without enough medical staff, hospitals close. Without enough workers,
supply chains break. Without enough policemen, laws cannot be enforced.
Without enough garbage collectors, cities grind to a halt. Without
enough cashiers, box stores cannot stay open. Without enough
administrators, institutions cease to function. Without enough staff,
corporations lose profits. Without enough servers, restaurants cannot
serve their customers. And without enough customers, businesses are
brought to their knees.
Tyranny is not sustainable if the system
grinds to a halt. Make it grind by being a thorn in everyone's side
until they give us back our freedoms and end this ridiculous charade.
They are trying to impose vaccine passports and mandatory vaccinations.
But we hold the cards... but only if we are bold enough to stand up even
at the risk of finding ourselves standing alone. Courage begets
courage. It was Martin Luther King's secret power. It must be ours.
Now
that you see the con, you also know the simple recipe to make this
virus go away before their reckless policies turn it a monster virus for
real. Remember 1918. End the war on the virus. Let the young folks come
out of the trenches. Let people go back to their lives. Provide focused
protection for the vulnerable. That is how this virus fades into the
history books.
It's time to be bold. It's time to call out the
fraudsters. And it's time to reclaim the habits, values, and principles
that are required to fix our democratic and scientific institutions to
prevent this from ever happening again.
Feudalism was one giant
stinking cesspool of self-serving corruption. Individual rights, free
markets, the democratic process, and limited government were the
antidotes that freed humanity from that hierarchical servitude. It seems
we have come full circle. The COVID con is a symptom, not the cause, of
a broken system.
Modern liberal democracy all around the world
was inspired by the system of checks and balances that America's
Founding Fathers built to prevent government from being co-opted by the
special interests of its leaders, institutions, corporations, and most
influential citizens. The ink was barely dry when those principles began
to be ignored by those with ever greater enthusiasm for an all-powerful
referee to manage even the most intimate details of how everyone lives
their lives. After two and a half centuries of effort the admirers of
big government have achieved their heart's desire. And what a glorious
and rotten cesspool of self-serving corruption it is.
But the
principles laid out by America's Founding Fathers remain as true today
as the day they were written and are waiting to be rediscovered. If
there is one culprit who deserves to shoulder more blame than any other
for the fiasco of the last 18 months, it is society itself for allowing
itself to fall prey to the siren song of big government, the illusion
that there can ever be a benevolent, virtuous, and incorruptible
referee. He who creates the red tape, he who has the keys to the
treasury, he who wields the power of the tax collector, and he who
commands those sent to enforce the laws will always have an entourage of
self-serving charlatans, rent seekers, and parasites following him
wherever he goes. So, keep his powers on a very short leash to keep
other people's hands off your money, your property, your freedom, and
your body. You don't need better leaders. You need less powerful
institutions. That's how you prevent this from ever happening again.
Freedom
of speech, individual rights, private property, individual ownership,
competition, good faith debate, small government, minimal taxes, limited
regulation, and free markets (the opposite of the crony capitalism we
now suffer under), these are the checks and balances that bullet-proof a
society against the soulless charlatans that fail upwards into
positions of power in bloated government institutions and against the
parasitic fraudsters that seek to attach themselves to the government's
teat.
Yes, we need a Great Reset. Just not the subscription-based version that the World Economic Forum imagined.
"Just Say No to Drugs"
“One
of the saddest lessons of history is this: If we’ve been bamboozled
long enough, we tend to reject any evidence of the bamboozle. We’re no
longer interested in finding out the truth. The bamboozle has captured
us. It’s simply too painful to acknowledge, even to ourselves, that
we’ve been taken. Once you give a charlatan power over you, you almost
never get it back.”
- Carl Sagan, The Demon-Haunted World: Science as a Candle in the Dark #Commissions Earned