Archive for the ‘vaccines’ Category

Adverse effects from COVID Shots Due to Stress Caused By ‘Anti-vaxxers’… Meanwhile in the Real World, Pathophysiology of the mRNA Molecule Explained As Sudden Deaths Continue

You seriously can’t make this stuff up…..

https://pubmed.ncbi.nlm.nih.gov/36381188/

Covid 19 vaccines and the misinterpretation of perceived side effects clarity on the safety of vaccines

Raymond D Palmer 1 2

Free PMC article

Abstract

In the era of Covid 19 and mass vaccination programs, the anti-vaccination movement across the world is currently at an all-time high. Much of this anti-vaccination sentiment could be attributed to the alleged side effects that are perpetuated across social media from anti-vaccination groups. Fear mongering and misinformation being peddled by people with no scientific training to terrorise people into staying unvaccinated is not just causing people to remain susceptible to viral outbreaks, but could also be causing more side effects seen in the vaccination process. This brief review will offer data that may demonstrate that misinformation perpetuated by the anti-vaccination movement may be causing more deaths and side effects from any vaccine. A mini review of published literature has been conducted and found that mental stress clearly causes vasoconstriction and arterial constriction of the blood vessels. Therefore, if subjects are panicked, concerned, stressed or scared of the vaccination, their arteries will constrict and become smaller in and around the time of receiving the vaccine. This biological mechanism (the constriction of veins, arteries and vessels under mental stress) is the most likely cause for where there has been blood clots, strokes, heart attacks, dizziness, fainting, blurred vision, loss of smell and taste that may have been experienced shortly after vaccine administration. The extreme mental stress of the patient could most likely be attributed to the fear mongering and scare tactics used by various anti-vaccination groups. This paper does not aim to rule in or out every side effect seen, but it is highly likely that many apparent side effects seen shortly after a subject has received a vaccine could be the result of restricted or congested blood flow from blood vessel or arterial constriction caused by emotional distress or placebo based on fear around vaccines.

_________________

**Comment**

Just who is this Raymond D Palmer, the author of this atrocious study?  The reason this is important is because this bogus study is posted on the U.S. government’s official website.

According to this, Palmer has a dubious background.

His Linkedin profile offers some clues (It appears his profile has now been deleted):

So he’s a mRNA Alchemist (pseudoscience) who speaks Chinese, and his top interest is Pfizer’s Albert Bourla.

Education-wise, he jumps from web design, to real estate, to electrical engineering. Then a course in astronomy and astrophysics. (Palmer is very into astronomy. This is his space photography site and this is a Perth Now feature on his 2009 solo space photography exhibition). Suddenly in 2019 he starts taking online courses in epigenetics, biochemistry, genetic engineering and the like. He publishes his first paper in a cardiovascular medicine journal the same year that he starts studying epigenetics, with no prior training in any related field.   Source

Please go here for more on his NIAID and NIH connections, NDAs, Hong Kong investors, and more.
And here for more crazy, unearthed information.

Palmer cites a single WHO-led study in support of this claim that post-vaccination adverse events are not causally linked to the vaccines.1  They simply worked off the presumption that the shots are not the cause of post-“vaccination” events, which ignores an immense body of literature demonstrating causal links.  Source

Palmer therefore hypothesizes that it must be those nasty “anti-vaxxers”.

Seriously, nothing shocks me anymore. There is ZERO integrity in science any more.

I wonder if Palmer truly understands what he is implying? He has completely snuffed out the “safe and effective” mantra by stating that the safety of “vaccines” is dependent upon the recipient’s psychological condition. 

You want to know what stresses me out?  Digital Vax Certificates. Go here to find out why.

It’s curious Palmer didn’t bother to mention the following very real stressors happening in the real world that have caused untold damage:

_________________

Meanwhile, back in the real world …..

https://popularrationalism.substack.com/p/on-the-sudden-death-pathophysiology?

On the Sudden Death Pathophysiology of the Vaccine mRNA Molecule

A Summary (for the General Public) and Commentary Regarding the Case Report Published by Dr. Michael Mörz (pathologist)

James Lyons-Weiler

Images in the Mörz article (See link) support the following hypothesis:

  • When the mRNA (that is embedded in the lipid nanoparticle of the Pfizer/BioNTech COVID-19 vaccine) is injected into the arm, the mRNA finds its way (via the blood stream) into distant cells—in this case endothelial cells that line the small blood vessels in the heart and brain. (The vaccine does not simply stay in the arm.)
  • Once in the endothelial cell(s), the mRNA instructs the ribosomes in the cell to manufacture spike protein.
  • The spike protein then migrates to the outer surface of the endothelial cell.
  • The immune system then recognizes the spike protein (or fragments thereof) as foreign and concludes that the endothelial cell has become infected.
  • Accordingly, the immune system sends lymphocytes and other inflammatory cells into the walls of the vessel to attack the presumed infected endothelial cell.
  • The vessel wall becomes inflamed (vasculitis) and, during this process, the endothelial cells become immunologically injured and may swell to varying degrees. Sometimes, abnormal intravascular coagulation (clotting within the vessel) may be triggered. In some instances spike protein may appear within the brain (or heart) tissue, where the spike protein may trigger an inflammatory reaction (encephalitis, myocarditis)

Originally Published on Notes from the Social Clinic, Nov 10, 2022

Brief summary by Dr. Rennebohm, author of the summary below: The Morz et al. study “documents the abundant presence of vaccinal spike protein in the capillaries of the brain and heart, and he shows how this is associated with vasculitis, necrotizing encephalitis, and myocarditis.”

(See link for article & in depth details)

________________

https://rumble.com/v1xxjz4-2nd-grade-student-suddenly-dies-kids-struggling-to-concentrate-post-vaccina.html  Video Here (Approx. 3 Min)

Canadian Doctor Reports on the Epidemic of Sudden Deaths

Doctor William Makis states an epidemic of sudden death taking effect in Canada overshadows dementia and heart disease to become Alberta’s top killer. Doctors who complied to a strict vaccine mandate to keep their jobs have had 3-5 shots and now 93 Canadian physicians (and counting) have succumbed to sudden death.

But it’s not just doctors who are dying suddenly.

Makis reports nurses, paramedics, police, firefighters, and teachers are also dying suddenly.  A second grade student just died.

Teachers are reaching out to Makis as they are seeing injuries and immune reactions, such as asthma, in children as well as the fact they aren’t able to concentrate in class.

Makis mentions the documentary “Died Suddenly,” which shows bizarre white, rubbery blood clots in the “vaccinated,” which can also been seen here and here.  He also mentions research that has been done where scientists have taken blood and exposed it to the spike protein, and the blood starts clumping almost immediately.  These proteins get built into the blood clots — amyloid proteins that make amyloid fibrils, which cause long clots that are very firm and rubbery. The body cannot degrade these clots, and doctors are finding that regular blood thinners don’t work.

If you are one of the unfortunate victims of these clot shots, please see The Spike Detox Guide put out by World Council for Health.

Category:

research, vaccines, Viruses

LymeX Prize Competition Announces Ten Phase 1 Winners

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/31127539

LymeX prize competition announces ten Phase 1 winners

Carl Tuttle

Hudson, NH, United States

NOV 30, 2022 — 

Please see the following letter sent to all winners of the LymeX prize…

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “contact@steveandalex.org” <contact@steveandalex.org>
Cc: The Tick-Borne Disease Working group and all winners of the LymeX prize
Date: 11/30/2022 1:12 PM
Subject: LymeX prize competition announces ten Phase 1 winners

November 7, 2022

LymeX prize competition announces ten Phase 1 winners
https://www.lymedisease.org/lymex-phase-one-winners/

“The ultimate goal of the multiphase competition is to nurture the development of diagnostics toward Food and Drug Administration review.” 

To all winners of the Phase 1 LymeX Diagnostics Prize competition,

After spending the last thirteen years studying the mishandling of Lyme disease, I felt compelled to share the following facts (and supporting documentation) regarding prior attempts to introduce “new and/or improved” diagnostic detection methods. I concluded that a chronic relapsing seronegative disease does not fit the business model of vaccine development, patent royalties and pharmaceutical profits so laboratory confirmation of persistent infection after antibiotic treatment must be squelched/suppressed at all costs.

Examples

1. Culture: Advanced Laboratory Services

Barbara J.B. Johnson, microbiologist with the Centers for Disease Control and Prevention claimed laboratory contamination in reference to positive test results (Chronic Lyme) found in Advanced Laboratory Services’ Borrellia culture test. If this is the case, why didn’t the CDC work with Advanced Laboratory Services to perfect its culture test and resolve the so-called “contamination” issues?

New Lyme Culture Test Failed CDC Analysis Aug 20, 2013
http://www.medscape.com/viewarticle/809626

New CDC/FDA Warning Against Unapproved Lyme Culture Test
https://www.medscape.com/viewarticle/823840

“Dr. Nelson emphasized that for Lyme disease diagnosis, the CDC recommends a 2-step process of serologic testing: first, an FDA-cleared enzyme immunoassay, followed in immunoassay-positive or equivocal cases by confirmatory Western blot. Only patients positive on both tests are considered to have Lyme disease.”

Carl Tuttle’s comment: Current FDA approved Lyme disease tests (Antibody tests) cannot be used to gauge treatment failure or success which makes them ideal for concealing an antibiotic resistant/tolerant superbug allowing the thirty-year-old dogma to remain intact.

2. PCR testing:

We have seen similar actions from the CDC with PCR testing as well. In May of 2012 the CDC announced the Development of a Novel Genus-specific Real-time PCR Assay for Detection and Differentiation of Bartonella Species and Genotypes:  http://www.ncbi.nlm.nih.gov/pubmed/22378904

Here the CDC is using PCR for a definitive diagnosis of Bartonella however, according to the CDC and the ALDF group on June 11, 2012 PCR cannot be used for Lyme diagnosis per the CDC expert commentary posted on Medscape below:

PCR for Diagnosis of Lyme Disease: Is It Useful? Christina A. Nelson, MD, MPH
https://www.medscape.com/viewarticle/764501

Quotes from Christa Nelson: (Medical Officer in the Bacterial Diseases Branch of CDC’s Division of Vector-Borne Disease)

“Is PCR useful for the diagnosis of Lyme disease? In general, the answer is no.”

“Two-tiered serology remains the mainstay of laboratory testing for Lyme disease.”

Carl Tuttle’s comment: PCR is acceptable for Bartonella but not Lyme disease. Double standard here?

3. Nested PCR and DNA sequencing: Milford Molecular Diagnostics

In September of 2012 the CDC entered into an agreement with Dr. Sin Lee to evaluate the viability of his DNA sequencing technology. Martin E. Schriefer, Ph.D., the chief of the CDC’s diagnostic and reference laboratory, stated the following: (from the attached court document)  https://www.dropbox.com/s/8irsb6oqunwy3zq/Notice%20of%20Appeal.pdf?dl=0

“So wherever possible we encouraged and required other non-serologic-based tests in addition to clinical presentation so that might have included PCR or culture or both. . . . And again I’m looking forward to seeing a greater utilization of PCR as a diagnostic tool in the future.” -Martin E. Schriefer, Ph.D.

When Dr. Lee published a case of persistent infection (Chronic Lyme disease) in 2014 all communication with the CDC ended abruptly with no explanation.

DNA Sequencing Diagnosis of Off-Season Spirochetemia with Low Bacterial Density in Borrelia burgdorferi and Borrelia miyamotoi Infections  http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139787/

Carl Tuttle’s Comment: It should be noted that the chronic Lyme disease case identified in this publication was found in blind-coded serum samples sent to Dr. Lee’s laboratory from the CDC’s Lyme disease serum repository and other species of Borrelia were found within these samples using DNA sequencing; the CDC had no idea that multiple pathogens were involved.

Has the CDC purposely discredited other innovative technologies which are in competition to the invention being patented by Theresa M. Russell and Barbara J.B. Johnson of the NCEZID under Pub. No. WO 2013110026 A1 entitled “Compositions and methods relating to Lyme disease”?

Dr. Lee although participated in the competition, was not awarded the LymeX prize. Does anyone believe that this decision was just a coincidence?

4. NIST

New Experimental Test Detects Signs of Lyme Disease Near Time of Infection February 11, 2016
https://www.nist.gov/news-events/news/2016/02/new-experimental-test-detects-signs-lyme-disease-near-time-infection

“The current standard blood test for Lyme disease exposes the infection only after antibodies have accumulated to detectable levels, which can take up to 4 to 6 weeks. If patients exhibit a telltale bull’s-eye rash, diagnosis and treatment can begin earlier. But the rash does not occur in 20 to 30 percent of Lyme disease patients, according to the Centers for Disease Control and Prevention.

Rather than waiting for an infected person’s immune system to produce noticeable amounts of antibodies, the team chose to home in on the bacteria itself—specifically, proteins the bug sheds when attacked by the body’s defenses.

“From many candidates, we chose one that is both easily distinguished from human serum proteins and an unambiguous indicator of the bacteria,” Turko says. “This protein, which resides on the outer surface of membranes, became the target of our search in serum samples.”

Carl Tuttle’s comment: Response from Dr Illarion Turko; “This project did not receive further development and is on-hold for now.”

So, who at the CDC got to Dr. Turko and discouraged further development?

Other examples of interference/intimidation

In 2008 Nordin Zeidner published his study regarding single dose Doxycycline for tick bite. Pamela Weintraub interviewed Zeidner for her book:

Cure Unknown (Revised Edition): Inside the Lyme Epidemic

By Pamela Weintraub

https://books.google.com/books?id=

Excerpt:

“Immunologist Nordin Zeidner, chief of the CDC’s Vector-Host laboratory in Fort Collins, Colorado, told me internal agency studies had found the strategy questionable, and definitely ineffective in mice.”

“With the support of his CDC colleagues, Zeidner had begun to work with industry to develop an alternative: a form of injectable Doxy that could be sustained in the body for nineteen days.”

“Trying his formulation on mice, Zeidner found that 100 percent were protected from Lyme as well as the coinfection, anaplasmosis.”

“…..single dose doxy stopped Lyme disease not in 87% of mice, but rather, in 20 to 30 percent at most.”

_____________________________

Dr Gary Wormser of New York Medical College (who has controlled the Lyme disease narrative for the past three decades) published a study earlier promoting the use of single dose Doxy for tick bite. (See Wormser’s 2001 flawed NEJM article)

I understand that it was Wormser who called Zeidner’s superiors at the CDC to put an end to Zeidner’s work. Zeidner was told to discard the mice sera instead of testing for antibodies as he had promised.

Zeidner’s research was terminated for “lack of industrial support” Mead, and he was promoted, and his email address inactivated. The CDC stopped his research and sent him to Europe

I have attached Zeidner’s 2008 study for your review:

A sustained-release formulation of doxycycline hyclate (Atridox) prevents simultaneous infection of Anaplasma phagocytophilum and Borrelia burgdorferi transmitted by tick bite
https://www.dropbox.com/s/jc0h9g9arjhc8l1/Zeidner%202008.pdf?dl=0

Questions for LymeX prize competition winners:

Are all of you confident that the current pandemic was handled properly by our Public Health Officials? Was diagnostic testing controlled/manipulated in any way? Have lifesaving therapies been suppressed over pharmaceutical profits (vaccines)?

I ask the competition winners to be suspect of HHS oversight for this LymeX prize competition and if any dishonest/suspicious activity is experienced as described previously in this letter, please seek early legal counsel, (perhaps collectively) and involve your state senators to expose the ongoing corruption hell bent at maintaining the false thirty-year Lyme disease narrative: “Lyme is Hard to Catch and Easily Treated” (with a 2-4wk antibiotic treatment mandated by the Infectious Diseases Society of America)

Respectfully submitted,

Carl Tuttle
Hudson, NH

Cc: All LymeX prize competition winners, All members of the 2022 Tick-Borne Disease Working Group, the Steven & Alexandra Cohen Foundation

More examples of interference/manipulation as reported through the experience of a clinician on the front lines:

2018 ILADS Webinar – History of Lyme Disease by Joseph J. Burrascano, Jr. MD. (Video Recording)
https://vimeo.com/306846706  Summary:

Joseph Burrascano, MD’s cogent history of Lyme: East Hampton, Long Island NY had the highest rate of Lyme in the world. 1965 internist Sidney Robin coined the term “Montauk Knee”.

1985   87 seronegative patients all had spirochetes produced using Alan McDonald’s culture technique. “Seronegativity is real”

@7:00  re: PTLDS – “There’s never, ever, ever been a description of this Post Lyme Syndrome from an immunological point of view that clarifies what it is and applies to every single patient”.

@9.05 Stony Brook study of 21 day doxycycline “… had a 100% FAILURE RATE… THEY KICKED ME OUT OF THE STUDY AFTER THAT; AND THEY NEVER REPORTED THOSE RESULTS.”

@9.35 Patient Evaluation: “I took advantage of Dr. McDonald’s culture… after treatment ended, if you waited a few weeks, they [patients] were all culture positive. It was failed treatment and a persistence of the infection.”

@12.45  Late 1980’s “Rocephin came onto the scene… 100% failure rate of 2 weeks of Rocephin, even at high dose… Duration of treatment is really, really what’s important.” Findings presented @ 1990 Stockholm International Conference.

@13.50  633 patient records reviewed indicated at least 4 months treatment for those “with multiple bites, Lyme arthritis, heart murmurs, hormonally active women, those sick for more than 1 year, age over 60, acute carditis, documented immune deficiency, failed oral treatment.”

@26.50 Discovered on lecture circuit Dr. Ed Masters from MO, John Druhl, NJ & Paul Levy, San Francisco all independently concluded higher doses and longer treatment necessary. They’d never met or communicated previously.

1990 NIH Gold Stain – 73 chronic patients, 13.5 months mean treatments. Discovered blebs and biofilms.

@31.19 “So, whatever happened to this great gold stain? Know what? Nothing. NIH stopped the funding… closed the whole thing down and never again did they ask front line Lyme doctors to contribute specimens to their studies. So, there’s some politics one more time.”

@32.58 Co infections seem to affect only chronic Lyme patients.

@34.19 Lyme is the thing that takes over the immune system, weakens our defenses….

@36.52 Lyme is an immune suppressive illness….

@38.25 McDonald presented cultures at “… a meeting of NYS Medical Society… detractors were people from Yale and Stony Brook who didn’t want their patented serologic tests to be usurped, and they started claiming that McDonald was falsifying his data and so forth.”

Category:

Activism, Lyme, Testing, vaccines

State of Control Documentary Just in Time: G20 (& Biden) Signs Declaration for International “Vaccine” Passport

**UPDATE**

Proving it’s all about control, the WEF is now demanding powers to regulate speech online.

https://debunkproductions.com/  Documentary & Trailer Here

State of Control Documentary

ABOUT THE MOVIE

“State of control”, of society is increasingly becoming a reality.

What is the price of convenience?

The CBDC (Central Bank Digital Currency) and the digital passport can make our lives easier and more efficient. But new international legislation shows that the purpose of these possibilities, has far-reaching implications for our privacy.

In this documentary international experts such as Edward Snowden, Arno Wellens, Catherine Austin Fitts express their serious concerns and criticisms. It compiles the range of facts and opinions, creating a shocking picture about the future of mankind. A crystal-clear narrative that can”t be ignored.

_______________

https://media.mercola.com/ImageServer/Public/2022/November/PDF/g20-signs-declaration-vaccine-passport-pdf.pdf  Go here for videos and article

G20 Signs Declaration for International “Vaccine” Passport

Analysis by Dr. Joseph Mercola

Nov. 30, 2022

STORY AT-A-GLANCE
  • The G20, a group of 19 nations — including the U.S. — plus the European Union, recently held their annual business meeting (B20) in Bali, Indonesia, where they declared that a digital vaccine passport, standardized by the World Health Organization, will be part of international pandemic prevention and response moving forward
  • The rule for standardized international vaccine passports will be introduced as a revision to the international health regulations during the next World Health Assembly in Geneva
  • The G20 recommendations also include the creation of guidelines for a globally coordinated response to crises, “enhanced by a technology-enabled ‘always-on’ global health infrastructure,” and a mutual recognition of COVID-19 vaccines made by G20 members
  • President Biden signed the declaration despite the promises made by his White House COVID-19 Response Team leader, Jeff Zients, who in April 2021 stated, “Let me be clear that the government is not now, nor will we be supporting a system that requires Americans to carry a [vaccination] credential”
  • The fact that the COVID shots do not prevent spread of infection has now been established many times over. This alone proves that vaccine passports are not for the purpose of containing epidemics. An international vaccine passport is the gateway to complete totalitarian control, because the entire control grid around a person gets tied together by it

As noted by former U.S. Rep. Dr. Ron Paul in the video above, World Economic Forum (WEF) founder Klaus Schwab and other globalist leaders substitute truth with their own opinions. They decide what’s right and wrong; they decide what’s right for everyone. They dictate what’s “true” on any given day.

Anyone who disagrees with them is an “enemy of the state” — they being “the state” or, more accurately, the Deep State, the hidden power behind the apparent power of official government. Who are the members of this cabal? There’s no official membership list, but over time many of the individual players have become discernible.

The globalist cabal includes but is not limited to government heads, bankers and members of nongovernmental organizations (NGO’s) and liberal think tanks around the world.

One way in which the cabal hides its undemocratic influence is by having its members in dozens of different organizations. When several organizations agree on an issue, it makes it appear as though there’s a majority view, a consensus. But in reality, it’s the same small group of individuals asserting their agenda.

G20 Green-Light International Vaccine Passports

The G20, a group of 19 nations — including the U.S. — plus the European Union, recently held their annual business meeting (B20) in Bali, Indonesia, where they declared that digital vaccine passports, standardized by the World Health Organization, will be part of international pandemic prevention and response moving forward.1

g20 signs declaration vaccine passportSource: Council on Foreign Relations2

Part of the policy declaration3 reads:4

“We support continued international dialogue and collaboration on the establishment of trusted global digital health networks as part of the efforts to strengthen prevention and response to future pandemics, that should capitalize and build on the success of the existing standards and digital COVID-19 certificates.”

The rule for standardized international vaccine passports will reportedly be introduced as a revision to the international health regulations during the next World Health Assembly in Geneva.5

What this means is that when the next pandemic is declared, only those who have this digital health certificate will be allowed to move about freely and travel internationally. And, of course, only those who have been appropriately tested and/or vaccinated will have a valid passport.

In addition to adopting an international digital vaccine passport, the G20 recommendations also include the creation of guidelines for a globally coordinated response to crises, “enhanced by a technology-enabled ‘always-on’ global health infrastructure,” and a mutual recognition of COVID-19 vaccines made by G20 members.

Schwab Tells Us What the G20 Are All About

Aside from key government leaders, high-profile globalists such as Schwab were also in attendance at the G20 meetings. In his B20 keynote address, Schwab highlighted the cabal’s agenda and goals:6

“What we have to confront is a deep, systemic and structural re-structuring of our world … [The] world will look differently after we have gone through this transition process.”

Part of that worldwide restructuring of society that the WEF, the G20 and many other organizations are working in lockstep to achieve is the implementation of a global vaccine passport, which all of the G20 members have now agreed to. In the case of the U.S., President Biden signed the declaration despite the promises made by his White House COVID-19 Response Team leader, Jeff Zients, who in April 2021 stated:7

“Let me be clear that the government is not now, nor will we be supporting a system that requires Americans to carry a credential. There’ll be no federal vaccination database, no federal mandate requiring everyone to obtain a single vaccination credential.”

If you’re a rational person, you’re probably thinking, “But wait, the COVID jabs don’t prevent infection or spread, so there’s no basis for vaccine passports anymore.” Indeed, this fact has now been established many times over. This alone proves beyond a shadow of a doubt that COVID vaccine passports have nothing to do with public health or safety.

Their purpose is not to prevent or contain pandemics. They’re a control mechanism,8 and a really important one. Vaccine passports are THE gateway to complete, totalitarian control of the populations of the world. The globalist cabal desperately needs everyone to have this passport, because the entire control grid around a person gets tied together by it. This is why fighting for informed consent is so crucial.

But how is the G20 getting around the obvious fact that the COVID passports are useless for their stated purpose? They ignore it, and instead stress that everyone also needs a digital identity, and this digital COVID certificate does both.

Outside their own circle, this rationale makes no sense whatsoever, but as noted by Dutch legal philosopher Eva Vlaardingerbroek, the fact that vaccine passports are sold based on a fraudulent premise is now “so obvious that they’ve thrown logic out the window.”9

Their decisions make no sense, and they have no intention of making them sensible. They’re banking on being able to entrap us in their control system, at which point they’ll be able to tell you the moon is made of cheese and you’ll have no way of correcting them without losing everything.

Digital Identity Is Total Surveillance to Control You

As reported by Sociable:10

“In August, 2021, the World Health Organization (WHO) published a 99-page guide book11 on the implementation of digital documentation of COVID-19 certificates, aka vaccine passports, stating that ‘a health pass based solely on individual vaccination status may increase the risk of disease spread.’

This is because the COVID-19 ‘vaccines’ were never proven to prevent transmission nor infection, and it recently came to light in the European Parliament that Pfizer never even tested its product for stopping transmission. Despite this knowledge being publicly available, the B20 is still recommending proof of vaccination as a means to travel …

Vaccine passports, by their very nature, serve as a form of digital identity, according to the World Economic Forum (WEF). A digital identity encompasses everything that makes you unique in the digital realm, and it is a system that can consolidate all of your most personal intimate data, including which websites you visit, your online purchases, health records, financial accounts, and who you’re friends with on social media …

[D]igital identity schemes can give governments and corporations the power to incentivize, coerce, or otherwise manipulate human behavior under a system of social credit. Digital identities can be used to determine what products, services, and information are available to us, and they can certainly be used by public and private entities to deny us that access.”

digital identitySource: World Economic Forum12

In March 2021, Naomi Wolf, author of “The End Of America,” warned that accepting digital ID will be the end of all freedom:13,14

“I cannot say this forcefully enough: This is literally the end of human liberty in the West if this plan unfolds as planned … Vaccine passports sound like a fine thing if you don’t know what those platforms can do.

I’m CEO of a tech company, I understand what this platform does. It’s not about the vaccine, it’s not about the virus, it’s about data. And once this rolls out you don’t have a choice about being part of the system. What people have to understand is that any other functionality can be loaded onto that platform with no problem at all.”

Liberty Counsel Founder and Chairman Mat Staver has also issued a warning, saying:15

“Digital health or vaccine passports along with tracking and tracing apps present a serious threat to freedom. Vaccine passports and tracking apps are about collecting data and control. The vaccine passport is being promoted worldwide to limit a person’s ability to leave home, work, shop, dine, travel, attend a public event, or even worship.

COVID is being used to advance this dangerous threat to freedom. We must never accept vaccine passports or tracking apps as the new normal. The implications for freedom are significant.”

Vaccine Passports Are Gateway for Complete Financial Control

When vaccine passports first became a topic of international discussions, many of us saw the writing on the wall and warned that such an implementation would become a tool for complete financial and physical control, and would automatically eliminate basic human rights and freedoms.

At the time, we were labeled crazy conspiracy theorists, but it didn’t take long before our worst fears were confirmed. Your vaccine passport will be your digital identity (as confirmed by the WEF), and to that digital identity they plan to add a programmable central bank digital currency (CBDC) and a social credit score. These plans are not a conspiracy theory. They’re out in the open.

When you add all of those ingredients together — vaccine requirements for maintaining a valid passport, a digital identity, a social credit score and programmable CBDCs — you end up with a control grid that will eliminate your freedom to live life according to your own desires.

Even your diet can then be dictated by these megalomaniacs. They’re hell-bent on eliminating your ability to eat meat, for example. The whole world, especially the Western world, must transition to insect protein, they say. Meanwhile, you will not find meal worms and crickets on the menus at their globalist gatherings.16 No, insect protein is for the expendables.

Once vaccine passports/digital identity and CBDCs are in place, the global cabal will be able to control your physical movements, behaviors and purchases based on how well you conform to their ideals, no matter how irrational, immoral, unethical, unfair or dangerous those may be. As reported by The Daily Sceptic:17

“It’s seemed evident for a while that the current fiat monetary system is, at best, unstable. At worst, it’s a Ponzi scheme whose time has expired. If that’s the case, I suspect the central bankers and 0.1% know this and might be prepared to usher in the new system before the old one collapses on itself — even as they loot it on the way down with the most significant wealth transfer in human history.

To anyone who pays attention to these trends, it seems evident that Central Bank Digital Currency (CBDC) will be that new system. Every indication is that CBDC’s arrival is imminent. [November 15, 2022], several global banks announced a partnership with the New York Federal Reserve to pilot digital dollars18,19 …

From my vantage point, it’s impossible to overstate the risk presented by CBDC. Whether it’s a utopian vision based on good intentions or a sinister plot to crush our sovereignty, the result may be the same: control. A Central Bank Digital Currency has all the downsides of fiat money, plus the added layers of surveillance and programmability overseen by the state.

So many people on Team Reality have likely felt like dissidents over the last few years simply for challenging anything beyond the herd mentality … Imagine a monetary system with features baked-in to socially engineer how we live. For example:

  • Health: ‘You didn’t take your booster … you’re not allowed in public spaces.’
  • Energy: ‘You used your energy allotment this month … your electric car won’t start.’
  • Food: ‘You ate too much meat this week … your money is only good for plants (or bugs).’
  • Savings: ‘If you don’t take your rations soon … your money will expire at the end of the month.’
  • Free Speech: ‘You shared info that we disagree with … our algorithm is fining you.’ (PayPal has already started doing this) …

As we saw with the lockdowns, China is the model emulated in the west. Like the creep towards health-related authoritarian measures, unelected globalists with financial interests lurk in the background …

If you have yet to notice, a primary theme of the last three-plus years (at least) is ‘freedom vs. control’, so it’s not hyperbole to suggest that the future must be decentralized if we want to ensure our children grow up in a free world.”

If there’s a silver lining in all of this, it’s that the globalist cabal — the “deep state” that pulls the strings of governments around the world, the hidden power that is making decisions that are devastating for the entire world — overplayed their hand during COVID, exposing their heinous ideologies and plans for all the world to see. As noted by Maajid Nawaz in an interview this past summer (video above):

“When dogma defines your behavior you’re no longer looking at reality … so you’re going to be less pragmatic … That leaves serious blind spots. You end up not seeing reality for what it is, and that is why they ended up overplaying their hand. They’re not looking to reality, they’re looking to their dream, their ideal, which is actually a nightmare.

One great thing that happened during COVID is they overplayed their hand. They exposed themselves … There’s now very little doubt, among those who have heard of the World Economic Forum, that it’s attempting to influence how we do government and politics …

Why do we have an unelected bureaucrat, and a foreign one at that, telling us how to live our lives …? It doesn’t make sense. But then we go further. Why do they all seem to be beholden to this unelected foreign bureaucrat? Why do they all appear to be doing this man’s bidding? … Why can’t they just say no?”

As noted by Nawaz, the government leaders who are not saying no to Schwab for some reason cannot say no, likely because they’ve been compromised. Compromising and blackmailing officials on behalf of the globalist cabal was Jeffrey Epstein’s specialty, and there’s no reason to assume their secrets died with him.

Those with cleaner records may have been threatened into compliance. I would add a third possibility, and that is that they’re in on it because they share the globalists ideals, which include not only top-down authoritarianism but also transhumanism and eugenics. A fourth possibility is self-preservation. They may simply want to secure their own position within the ruling echelon in the new world of “have it alls” and “have nothings.”

We Now Know What They’re Capable Of

Whatever the incentive, the problem they now all face is the fact that they’ve prematurely exposed themselves and their plans. They’ve also exposed how far they’re willing to go. For example, we know they’re willing to seize your bank account and close down your ability to transact over something as minor as making a donation to a cause they don’t like or posting “wrong”-think on social media — and that’s without the benefit of CBDCs!

So, they’ve already shown us what they WILL do once CBDCs are in place. The only difference is that penalties can then be automated. Is this a world you want to live in? Is this what you want for your children and grandchildren? If not, it’s your duty to be the resistance.

Adults today are the last generation that will be able to prevent this global tyranny. If we do nothing, our children will be ensconced in a digital prison they won’t be able to break free from. So, we cannot leave it to them. It’s up to us. So, when CBDCs are rolled out, we must reject them, no matter how inconvenient that might be. When vaccine passports are rolled out, we must reject them, despite the limitations that might bring.

In 2021, countless people were coerced into taking the jabs because they wanted to travel, fearing travel bans for the unvaccinated would be permanent. Well, they weren’t, because enough people pushed back.

We may have to endure limitations if we refuse the coming international vaccine passport, but if enough people around the world refuse, the system won’t work, and those limitations will prove to be temporary. The only way any of the globalists plans can become permanent is if we do as we’re told and go along with them.

– Sources and References

For more:

The past two years have shown good papers being retracted and bad papers being published.  One thing is for sure, 5G is moving forward because without it, the ‘powers that be’ can not track and mine all of our information.  This information will also include personal medical records, personal banking records, school records, and every financial transaction you make.  What you say and do can and will be used against you and we will be incentivized to “do the right thing.” Dissenters and protestors will be sanctioned and fined and sheeple will be rewarded and privileged.  And this doesn’t even delve into the health issues that will crop up due to 5G which are already being seen.

Category:

Activism, vaccines, Viruses

Ex-Pharmaceutical Industry & Biotech Exec: Massive Regulatory and Manufacturing Fraud With C-19 Injections. Pfizer CEO Who Said “Misinformation” is Criminal, Found Guilty of “Misleading” COVID Shot Claims

https://media.mercola.com/ImageServer/Public/2022/November/PDF/covid-19-vaccine-regulatory-manufacturing-fraud-pdf.pdf

Go here to watch Lena’s interview with Latypova.

C-19 Injections: Massive Regulatory and Manufacturing Fraud

Analysis by Tessa Lena
Nov. 22, 2022

STORY AT-A-GLANCE

  • Alexandra Latypova is an ex-pharmaceutical industry and biotech executive with a lot of experience in the areas of drug safety and clinical trials
  • Early on, she discovered that, based on the number of reported deaths and adverse events per lot, there was unprecedented variability in the toxicity of the product
  • According to Alexandra, the mRNA shots do not conform to their label specifications, and “in practice, both ‘blank’ and ‘lethal’ vials and anything in between is produced”
  • Having analyzed massive amounts of publicly available data, as well as documents that became available as a result of FOIA requests and other sources, she has found strong evidence of manufacturing and regulatory fraud

I recently had the pleasure of interviewing Alexandra Latypova, an ex-pharmaceutical industry and biotech executive, who has been investigating and exposing manufacturing and regulatory fraud related to COVID injections.

We talked about the industry standards that were not adhered to during the clinical trials and the manufacturing of those injections, about the vial content quality testing procedures that had not been put in place, about the “hot batches” and their geographical distribution, about signs of fraud at every stage of testing and manufacturing the product, and about the general condition of living in a world run by a mob.

The latter was the lightest part of our conversation — evoking a lot of dark Eastern European humor — since both of us are Soviet expats, and in 2020, neither of us required a whole lot of imagination to embrace the existential possibility of living in a world run by a mob. We had seen it in the past without a disguise — and when something looks like a duck, walks like a duck, and quacks like a duck, maybe it’s just a duck!

Alexandra Latypova’s Background

Alexandra grew up in Soviet Ukraine and immigrated to America in the late 1990s. She received her MBA from Dartmouth College and the spent about twenty five years in pharmaceutical industry and biotech (including in the areas of drug safety and clinical trials).

Alexandra has had a very gratifying entrepreneurial career. She has founded a number of successful startups, sold them — all before COVID — and retired, hoping to focus on enjoying her life and especially painting, which she does masterfully.

When 2020 knocked on the door with a whole bag of ugly and weird “new normal” treats, Sasha smelled the rat right away. Initially, she became alarmed by the abnormalities in “COVID response,” including the very conspicuous campaign to prevent effective treatment of COVID.

Compelled to understand what was going on, Alexandra got to work. She looked at VAERS and discovered huge discrepancies between the lots, where some batches had just a few reported severe adverse events, and some had over 1500 (she later learned from FOIA’ed documents that lot sizes were in a relatively similar range, and thus the discrepancies could not be explained by the lot size).

And when it comes to VAERS, let’s not forget the 2010 Harvard Pilgrim study showing that VAERS was severely underreported — NOT overreported — capturing less than 1% of adverse events.

“Hot Batches”

Early on, Alexandra discovered the existence of “hot batches.” She is one of team members behind the famous “How Bad Is My Batch” webpage where people can look up the number of severe adverse events reported to VAERS associated with a COVID injection lot number. Other fearless members of the team are Dr Mike Yeadon, ex-head of Pfizer Respiratory Research, Jessica Rose, statistician, Craig Paardekooper, researcher, and Walter Wagner, lawyer.

The slide below show the unprecedented variability of serious adverse events and deaths in the U.S. per batch. Note the comparison to the variability of the flu vaccine lots.

covid-19 vaccines serious ae and deaths

In the interview, Alexandra also mentioned the uneven distribution of deaths per a hundred thousand doses from batch to batch in the U.S. The coasts did much better than some of the Midwestern states that showed a very high numbers of reported deaths per a hundred thousand doses. The worst state is South Dakota (30+ reported deaths per 100,000 doses).

The areas that did even worse, according to Alexandra, were some of the U.S. territories with high percentage of indigenous population. (The latter data became available after the presentation was created, not reflected in the slide.)

vaers deaths 100k after vaccination

“Garbage Soup”: Non-Compliance With Good Manufacturing Practices

In the interview, Alexandra calls the COVID injections products “garbage soup,” both due to the massive non-compliance of the vial content to the specifications (per multiple independently done tests) — as well as due to their non-compliance with Good Manufacturing Practices. Wait, are the manufacturers trolling us? Are telling us that they do not comply (but we must)?!

There are many theories about what’s behind for such wild inconsistency between batches, from manufacturing defects to deliberate toxicity testing — and anything in-between. In her TrialSiteNews article, Alexandra tackles one important angle of the challenge that so many of us had to “explain” when talking to the friends of a more mainstream persuasion:

“Many of us are familiar with the following conundrum: on one hand, highly credentialed scientists and doctors have written numerous research papers explaining the dangerous mechanisms of action underlying mRNA/DNA “platform” technologies. The papers are meticulously researched and depict, correctly in my opinion, many terrifying consequences of the technology that breaches the innate protective mechanisms of human cells.”

“Furthermore, these theoretical papers are validated by the observed outcomes, such as for example, increases in all-cause mortality in high correlation with increases in rates of vaccination in a given territory, unprecedented increases in the adverse events and deaths recorded by various passive reporting systems, astonishingly high reports of the adverse events and deaths from the pharmas’ own pharmacovigilance systems, and autopsy findings in vaccinated post-mortem showing the mechanisms of mRNA technology damage in histopathologic evaluations.

On the other hand, many who have received the injections report no adverse effects and deem the points above a ‘crazy conspiracy.'”

“The question from the uninjured seems to be – why don’t we see MORE deaths if what you say about mRNA products is true? Setting aside ethical limitations of this question, here is a possible answer why: The mRNA shots do not conform to their label specifications. In practice both “blank” and “lethal” vials and anything in between is produced [emphasis mine].”

Like I wrote earlier on my Substack, “remarkably, some analyzed vials were reported to contain left over magnetic beads (magnetic beads are used in production of mRNA). Remember the “crazy” videos of some people developing magnetism in the place of injection? Now we have a new, ‘non-conspiratorial’ explanation for the ‘conspiratorial’ videos! Yay, following the science!”

According to Alexandra, vials of mRNA injections are not routinely tested by the manufacturers for conformity to the label. She notes that “the more they conform to the mRNA specification, the deadlier they seem.”

The only vial-level tests specified, for instance, by Pfizer, in leaked Chemistry Manufacturing and Controls documents, are the vial weight at filling, manual inspection for large visible particles, and some tests related to integrity such as vial capping.

The documents don’t describe no routing vial or dose tests verifying the ingredients. Each Pfizer dose is supposed to contain 30 mcg of mRNA, as stated on the label, but there is no information about any testing done to verify that.

“The ingredient conformity tests described in Pfizer CMC package are based on the bulk product batch testing – an upstream manufacturing process step.

It is a regulatory requirement to retain samples of each batch produced, and these samples of vials should exist and be available for examination. Per contracts with the US Government/DOD, the product is shipped to the DOD who retains the ownership of the vials until the product is injected into people.”

Alexandra notes that those contracts are very detailed and specify manufacturing data to be delivered to the DOD, however, she not find any descriptions of sampling of the vials for purposes of verification of their contents vs the label. “Furthermore, it is expressly forbidden by the international vaccine supply contracts to perform the vial tests for label conformity.”

Evidence of Collusion

In the interview, as well as in this article, Alexandra talks about the evidence of collusion between the manufacturers, the global regulatory agencies, and the US Department of Defense.

Having analyzed various public data from CDC’s VAERS database as well as various documents that have been obtained through FOIA releases and other source, she concluded that such collusion “led to the commercial release of the Covid-19 countermeasures that do not comply with the current Good Manufacturing Practices (cGMP).”

Evidence that Alexandra talks about includes Moderna’s non-clinical study summaries, Pfizer’s Chemistry Manufacturing and Controls documentation, and contracts between pharma and the DOD for supply of the mRNA/DNA products. According to her, “it reveals disregard for established safety rules, regulations, and safety practices throughout the development, manufacture, and distribution of these products.”

Moderna Red Flags

As reported by Children’s Health Defense, Alexandra reviewed 700 pages of documents that Moderna submitted to the FDA as part of its application process and obtained via a Freedom of Information Act request.

And according to her, “out of nearly 700 pages, about 400 pages are irrelevant studies that Moderna repeated multiple times. Moderna also submitted three versions of a single module, she said. And one module contained only narrative summaries of Moderna’s studies, but no actual study results.” Alexandra’s conclusion is that we are missing a large number of results, such as full reports that would support their narrative.

“The FDA ‘obviously did not object’ to any of this, she said. ‘That’s evidence of collusion to me with the manufacturer.'”

Other “abnormalities” that Alexandra highlighted both in the interview and in the Children’s Health Defense article, were Moderna’s clinical trials timeline and the fact that their product has two — not one — Investigational New Drug (IND) number.

Normally, there is one IND application for one product. “In this case, however, there are two IND applications — one belonging to Moderna, and one belonging to the National Institutes of Health, which partnered with Moderna on its COVID-19 vaccine.”

“The Investigational New Drug (IND) application meeting is supposed to occur with the FDA when the company initiates human clinical trials. Moderna and the FDA had a pre-IND meeting on Feb. 19, 2020, and the IND application was formally opened the next day. The global pandemic was declared on March 11, 2020.”

In the words of Alexandra, “Somehow these visionaries could predict the future with such certainty that they opened a clinical trial for the vaccine, for which a pandemic was announced a month later.”

Pfizer Red Flags

As Alexandra notes in her article titled, “Did Pfizer Perform Adequate Safety Testing for its Covid-19 mRNA Vaccine in Preclinical Studies? Evidence of Scientific and Regulatory Fraud,” “both the manufacturer and the regulators behaved in a highly dishonest manner and conspired to push an entirely novel technology and product on millions of people without carrying out a single well designed safety assessment.”

For example, she points out that a review of clinical studies released by FOIA uncovered that at least 4 different variants of active ingredient were included in the single Investigational New Drug application by Pfizer IND#19736:

  • BNT162a1 — Unmodified mRNA (uRNA; variant RBL063.3)
  • BNT162b1 — Methylpseudouridine-modified mRNA (modRNA; variant RBP020.3)
  • BNT162b2 — Methylpseudouridine-modified RNA (modRNA; variant RBP020.2)
  • BNT162c2 — Self-amplifying unmodified mRNA (saRNA; variant RBS004.2)

Alexandra writes that while the use of multiple versions of a product in the early stages of development is often inevitable, each chemical or biological entity is nevertheless deemed legally distinct for the purpose of product approval.

“Therefore, studies conducted with versions of the product that don’t conform to the exact specification of the final version may serve only as supporting information for the approval of the latter, but they should never be deemed definitive and sufficient tests for claims of safety or efficacy pertaining to the final product.”

She further mentions that in September 2021, the FDA issued a draft guidance entitled “Studying Multiple Versions of a Cellular or Gene Therapy Product in an Early-Phase Clinical Trial,” which states that each version of product requires a separate IND application.

However, stunningly, “a footnote in this guideline exempts ‘vaccines intended to prevent infectious diseases’ from this requirement. No explanation is given as to why this exemption is made, and no conceivable scientific or legal basis exists for this exemption, other than that the FDA had already arbitrarily allowed this unprecedented deviation from the regulatory standard and later needed to cover their tracks.

In fact, arguably this regulatory ‘exception’ does not even apply to Pfizer’s COVID-19 ‘vaccine,’ since the product does not prevent infection or transmission of the disease. Is intent to prevent illness alone a sufficient condition? After all, every new drug is intended to do something like preventing an illness, but only few successfully do so.”

Alexandra’s article is very detailed, and I highly recommend reading it in full. You can also find Alexandra on TrialSiteNews and on her Bitchute channel. To summarize her take on Pfizer, she make the following points:

  • Pfizer’s program did not include a comprehensive end-to-end test of all components of the final approved product (the mRNA COVID-19 vaccine). Instead, the studies included in the document package submitted to the FDA employed several variants and analogues of the product, whose comparability to the actual COVID-19 vaccine was not demonstrated or evaluated.

Thus, no comprehensive assessment of product safety can be made on the basis of these studies.

  • A key determinant of a drug’s toxicity is its distribution within the body. However, with the mRNA active ingredient of Pfizer’s COVID-19 vaccine, this crucial aspect was never studied!
  • Pfizer claimed absence of potential for “vaccine-elicited disease enhancement” based on studies of an animal species that does not get sick from SARS-CoV-2.
  • The CDC, the FDA and Pfizer all lied about “vaccine staying at the injection site;” they knew all along that distribution of the vaccine throughout the body had to be expected.
  • Pfizer skipped major categories of safety testing altogether.
  • Pfizer used dishonest and self-serving interpretation of regulatory guidelines to justify the shortcuts it took in routine safety testing.
  • Both FDA and Pfizer knew about major toxicities associated with gene-therapy medicines in general, and they therefore cannot claim lack of anticipatory knowledge of these risks with the particular gene therapy medicine that is Pfizer’s COVID-19 vaccine. This points to intentional fraud and collusion between Pfizer and the regulators, who conspired to push this untested dangerous product on the market.

Yes, They Are Trolling Us — But We Are Not Helpless

Even though it is rather disheartening to know we live in a world that run by a mob, the challenge is centuries old, and remembering it can bring us much needed perspective and balance. The novel and “sudden” part of the challenge is that is happening to us, here and now, in broad daylight. That’s shocking! But throughout history, many of our ancestors had to deal with tyrants, and today, it is our turn to be brave. May our brave ancestors be our inspiration.

I would like to end this story with a short quote from my earlier article titled, “Is Our World Run Like a Mafia? So What Do We Do?:”

“Good news: As the mafia bosses do their predatory thing, something mysterious is happening the hearts of those of us who insist on love. Under pressure, we are forced to remember that we are not theirs.” We are not theirs. It is true.

About the Author

To find more of Tessa Lena’s work, be sure to check out her bio, Tessa Fights Robots.

________________

https://reclaimthenet.org/pfizer-ceo-misleading-vaccine-statements-regulator/

Pfizer CEO, who said online “misinformation” is criminal, is found guilty of “misleading” vaccine statements

A regulator has ruled.

By Cindy Harper

Nov. 27, 2022

SUMMARY:

  • Bourla called people who spread COVID-19 vaccine misinformation “criminals,” in his calls for censorship of misinformation online.
  • A parent campaign group UsForThem filed a complaint with the Prescription Medicines Code of Practice Authority (PMCPA) has accused Bourla of violating clauses of the code of practice by the Association of the British Pharmaceutical Industry (ABPI) by making “disgracefully misleading” and “promotional”comments about vaccinating children.
  • The parental complaint states there is no evidence that healthy kids are at significant risk from COVID.
  • The complaint also states Bourla failed to present information in a factual and balanced manner, thereby misleading the public by making unsubstantiated claims.
  • A PMCPA panel found Bourla did violate the code of practice in many ways.
  • Pfizer appealed the ruling by stating Bourla’s remarks were based on provable, scientific evidence.
  • The panel upheld the complainant’s claims but ruled against claims that Pfizer discredited the industry, encouraged reckless use of a treatment, and did not maintain high standards.

(See link for article)

Category:

Activism, vaccines, Viruses

News You Won’t Hear: Vitamin D Reduces COVID by 20%, Mortality by 33%, But More COVID Theatre

https://popularrationalism.substack.com/p/vitamin-d2-and-d3-study-retrospective

Vitamin D2 and D3 Study Retrospective Study

220,000 veterans given D3… Large retrospective study… 33% reduction in mortality rate… Should IPAK do a prospective RCT on Vitamin D3 supplementation?

James Lyons-Weiler

John Campbell reviews a study published November 2022.

Gibbons JB, Norton EC, McCullough JS, Meltzer DO, Lavigne J, Fiedler VC, Gibbons RD. Association between vitamin D supplementation and COVID-19 infection and mortality. Sci Rep. 2022 Nov 12;12(1):19397. doi: 10.1038/s41598-022-24053-4. PMID: 36371591; PMCID: PMC9653496.

The study found (among other very promising results):

  • 20% reduction in COVID-19 cases in people receiving D3.
  • 0.23% mortality rate, 33% mortality rate reduction in people receiving D3.

While it’s not a RCT, John emphasizes that no one will do an RCT on D3 because there is no money in it, so no one will fund it.

http://  Approx. 20 Min

Vitamin D: Safe and Effective for COVID

Dr. John Campbell

Conclusions:  These associated reductions in risk are substantial and justify more significant exploration and confirmation using RCTs.

These will never happen, just like many topics with Lyme/MSIDS will never happen, and for the same reasons: money.  Nobody wants to study something that won’t be a “cash cow.”  Also, researchers are well aware of the need to push the government narrative and the fact studying cheap drugs/supplements isn’t popular and will not receive government funding.  The ‘powers that be’ are pushing a “climate change” agenda and all new studies must push this somewhere in order to receive training.

__________________

https://www.theepochtimes.com/health/will-you-survive-the-tripledemic

Will You Survive the ‘Tripledemic’?

‘Experts’ warn of pending doom
Joseph Mercola
Nov 9 2022
The first-ever RSV vaccines are now in the pipeline, directed at pregnant women, newborns and seniors. (Justin Sullivan/Getty Images)
The first-ever RSV vaccines are now in the pipeline, directed at pregnant women, newborns and seniors. (Justin Sullivan/Getty Images)
According to mainstream media, a winter triple-blizzard of disease is headed our way and hospitalizations are already on the rise. But this time, although they won’t admit it, it’s not the unvaccinated most at risk. Are we on track for insane COVID measures to resume?

STORY AT-A-GLANCE

  • According to mainstream media, hospitalizations for respiratory infections are on the rise and “experts” warn of a potential “tripledemic” this winter, as COVID, seasonal influenza and respiratory syncytial virus (RSV) are all in circulation
  • The U.S. Centers for Disease Control and Prevention reports a 1% increase in new admissions of patients with confirmed COVID-19. Maine — which has one of the nation’s highest COVID jab rates — has the most COVID hospitalizations. RSV cases are also unseasonably high
  • “Health experts” are now calling for voluntary indoor masking again, even though all the evidence garnered over the past three years confirms that face masks cannot prevent viral infection and spread
  • The first-ever RSV vaccines are now in the pipeline, directed at pregnant women, newborns and seniors. Some of them are based on mRNA technology
  • No vaccine for RSV has ever been successfully developed before, because the vaccines had a persistent tendency to cause worse disease, a phenomenon known as antibody-dependent enhancement (ADE)  (See link for article)

Important excerpt:

Do you really want to go through all of that again? If not, just say “no” from the start. Say no to masks. Say no to social distancing. Say no to canceling the holidays. Say no to lockdowns. Say no to flu vaccines and COVID shots. Just say “NO” to their fearmongering and live your life.

Fear is a tool used to control you, but that only works if you buy into it.

And speaking of fear, Fauci and HHS are back spreading it liberally:

HHS believes a new wave of COVID should cause everyone to social distance and mask up  again, despite the fact masks don’t work for viruses and lockdowns were proven to be ineffective and devastating on many levels.  They also somehow believe masking will prevent long COVID (and evidently racism) despite many stating masks may actually contribute to long COVID by causing hypoxia and rebreathing of the virus and other bacteria by the wearer.  And Fauci, true to form before exiting stage right, wants everyone to make sure to get their COVID and flu shots, despite the fact the COVID shots have negative efficacy, and have caused more adverse reactions and death than any other “vaccine” in the history of VAERS. Big Pharma now is planning to combine the COVID & flu shots into one so everyone gets that mRNA technology into them whether they want it or not. 

Regarding the flu shot:

  • The flu vaccine increases COVID-19 infection by 36%, and the flu vaccine alone increases the risk of contracting a non-flu respiratory illness by 65%. 
    • In fact, rising case numbers of RSV, the most common respiratory virus in children, have been reported across the U.S. Immunity has been suppressed due to being sheltered in place and not getting usual exposures to viruses, as well as due to the COVID shots causing immune suppression – setting people up for illness.  But of course corrupt public health has ONE singular answer: get yet another shot, and quickly create another lucrative “vaccine” for it.
    • According to Robert F. Kennedy, the crisis “has become a vehicle for re-implementing the COVID-19 playbook all over the country and responding with vaccines.”
  • The flu shot, like the COVID shot, doesn’t prevent the spread of the flu or prevent death, and is also notoriously ineffective as well as dangerous.
  • It was announced early in 2022 that the dominant strain circulating doesn’t match the vaccine, and that it isn’t that effective, yet for some reason we should still get it.  (Sound familiar?)
  • There is a very strong correlation between getting the flu shot and dying from COVID if you are 65 or older.
  • Similarly to the fraudulent COVID shot studies, a 2018 Cochrane review found that only 15% of flu research studies were well designed and conducted, and concluded:

recommendations for routine use of influenza vaccine as a routine public health measure was not supported by the published evidence base.

But truth be damned.  When you are NIAID mafia overlord, you can say what you want even if it’s all false.

It’s worth reposting this 2014 video of investigative journalist Harry Vox as everything he predicted as come true:

http://

“Scenarios for the Future of Technology and International Development”

By the Rockefeller Foundation in 2010

Lays out the “Lockstep” scenario which details the global response being used

These people will stop at nothing to push their lucrative, dangerous injections.

Category:

Activism, vaccines, Viruses