More LIES and CONtradictions About COVID and the Vaccines | How Does Anyone Still Believe the Narrative?

We have been lied to numerous times by top officials. When will the rest of the world wake up?

A video that has gone viral in the last few days exposes medical “authorities” proposing underhanded tactics and straight up lies and fear-mongering attempts in order to push vaccines onto more of the public.

There have been many attempts at deceiving the public regarding the COVID/vaccine narrative, or just flat-out conflicting information that doesn’t make any sense when actually thinking about the statements.

The below sections take a look at just a small few of them, starting with the video mentioned above:

1. Novant Health administrator suggesting to deliberately scare/manipulate people into getting the vaccine:

Some embellishment is added for emphasis. Some words were undetermined due to unclear audio:

Carolyn Fisher: ” – the dashboard on how it’s set up myself, as far as how we get information out to the community on meaningful numbers – we set on a weekly basis. So that’s on our website, and we’ve been sharing that through social channels as well. Particularly those graphics that show the number of patients and how’s the percentage of them that are unvaccinated – percentage of unvaccinated people in the ICU, and the percentage of deaths. And the numbers. So those are numbers that we put out as far as, we don’t get into details of floor – Those other numbers are certainly out there.”

Mary Kathryn Rudyk: “I guess my feeling at this point in time is, maybe we need to be completely, a little bit more scary for the public. Then there’s another […], that I completely agree, there are many people still hospitalized that we’re considering post-COVID. But we’re not counting in those numbers. So how do we include those post-COVID people, in the numbers of patients we have in the hospital?”

Carolyn Fisher: “So is that all the people who have been in a hospital since the beginning of COVID?”

Mary Kathryn Rudyk: “Well, or those that are still in, and that’s something that I can take to someone else. But, I think those are important numbers, of patients that are still in the hospital, that are off the COVID floor, but still occupying the hospital for a variety of reasons.”

Shelbourn Stevens: “Carolyn, we call those – I’m sorry – we’re calling those “recovered” now; if you look at the […] dashboard, they’re listed as “recovered”. But I do think it – from our standpoint, we would still consider them a COVID patient, cause they’re still healing.”

Mary Kathryn Rudyk: “Yep. So I think that that needs to be highlighted as well. Because once they’re off isolation and drop from the COVID numbers, that’s exactly right.”

Shelbourn Stevens: “Carolyn, we can talk offline, and how we run that up, to marketing.”

Mary Kathryn Rudyk: “Right. So I was going to say that I think we have to be more blunt, we have to be more forceful, we have to say something coming out, ‘You know, you don’t get vaccinated, you know you’re going to die.’ I mean, let’s just, let’s just be really blunt to these people.”

There’s a lot to unravel in this brief discussion, but it all boils down to this: Mary Kathryn Rudyk suggests inundating the public with FEAR that COVID is such a deadly disease and that if you don’t get vaccinated, ‘you’re going to die’; yet in the very same discussion, acknowledges that there are many people who have recovered from COVID and are sometimes referred to as “post-COVID”.

Then if one wants to further expand upon this discussion, alleging that Rudyk is announcing this to also try and benefit the healthcare workers so that they are not overwhelmed with COVID-infected (or COVID-recovered) patients, I would have to bring up the point that there have been prophylactic treatments available to help prevent one from going to the hospital, yet these treatments are being SUPPRESSED from the public and denounced all around the healthcare industry and mainstream media/social media platforms.

If it’s about our health, then why are approved, well-known, beneficial, effective treatments being taken away from public use and ridiculed, and even in some cases, outlawed?

Maybe it’s because… it’s not about our health?

2. American Medical Association trains their healthcare members to label “hospitalization rates” as “deaths”

Another health organization that has been caught directly trying to lie and manipulate the public has been exposed by what they are training their associates to say in order to either sugar-coat certain terminology, or by outright blatant fear-mongering attempts in order to produce the results they want. (i.e. more and more people getting vaccinated)

At first, I couldn’t believe this was really real, until I checked it out for myself; and indeed, it is all stated there, right on the pdf of their website.

This information was first brought to my attention through the Stew Peters Show with Dr. Bryan Ardis. The video describing some of the incredibly outrageous deceptive tactics the AMA teaches members of its organization can be watched below:

A couple of screenshots are provided, with a link from the web archive:

Screenshot taken on September 14, 2021 from
[ https://www.ama-assn.org/system/files/2021-02/covid-19-vaccine-guide-english.pdf / pg. 9]
Web Archive version: COVID-19 Vaccine Guide

Instead of “Operation warp speed” – say “Standard process”
Instead of “Government” – say “Public health agencies”
Instead of “Hospitilization rates” – say “Deaths”

There is also the eerie, cult-like mentality that the AMA endorses their members to propagate on social media platforms and during interviews. A small portion of that has been captured in the below screenshot:

Screenshot taken on September 14, 2021 from
[ https://www.ama-assn.org/system/files/2021-02/covid-19-vaccine-guide-english.pdf / pg. 2]
Web Archive version: COVID-19 Vaccine Guide

– “I will get vaccinated as soon as it is available, as will my family. #TrustScience #COVID19”

– “I trust the scientific process and the rigorous peer review for the coronavirus vaccines. #TrustScience #COVID19”

– “I trust a vaccine endorsed by scientists, career public health professionals, my doctor, and the mainstream medical community. #TrustScience”

The egregious step to label “hospitalization rates” as “deaths” aside, which is insane as it is, I couldn’t help but get chills when reading the indoctrination-like proclamations of the social template content.

That is exactly what these industries and agencies want: blind trust to those in “authoritative” positions.

3. Israeli Health Minister caught on hot-mic: “there is no medical or epidemiological justification for the COVID passport, it is only intended to pressure the unvaccinated to vaccinate.”

I don’t expect the tweet to last long (perhaps I’ll be proven wrong), so I have provided a screenshot of the snippet in question:

Source: twitter | @disclose.tv

I can’t personally verify the translation since I don’t speak the language, but the following excerpts come from the following source: Caught on hot mic, Israeli health minister says ‘green pass’ not based on epidemiology

“Imposing “green pass” rules on certain venues is needed only to pressure members of the public to get vaccinated, and not for medical reasons, Israeli Health Minister Nitzan Horowitz said on Sunday, ahead of the weekly Cabinet meeting.

Horowitz was caught on a hot mic telling this to Interior Minister Ayelet Shaked, who was also unaware that the conversation was being taped and would be broadcast on Channel 12 News.

In response to Shaked’s suggestion that the “green pass” could be removed as a requirement for outdoor seating at restaurants, Horowitz said: “For swimming pools, too, not just in restaurants.”

“Epidemiologically, it’s true,” said Horowitz, adding, “The thing is, I’m telling you, our problem is people who don’t get vaccinated. We need [to influence] them a bit; otherwise, we won’t get out of this [pandemic situation].”

Here is another resource for further consideration:

Source: twitter | @EdladYaniv

Text translated using: Hebrew to English translation

“And now the unbelievable video is that it is exactly the opposite of what The Minister of Health told The High Court:

Health Minister Nitzan Horwitz explains to Sarah Ayelet Shaked that in some places the green giver is not necessary and is only to pressure Israelis to get vaccinated.

And this is exactly the opposite of what the Health Minister told The Begach “that the green tag is net health considerations.”

And this is Chairman Meretz.”

More lies, more influencing, more pressure, more threats, more deception.

When will the world wake up?

4. Vaccines and vaccine passports are only valid for 6 months. After that – you need more vaccines.

Again highlighting Israeli’s Health Minister, Dr. Horowitz, who has admitted that the vaccines are not about one’s health, is implementing the following protocols for their country – another under-handed tactic that is being used to trick the public into more unnecessary vaccines.

“Israel’s vaccine passport QR-code system, Green Pass, will now expire six months after the second injection is received, making a third, and possibly fourth, booster shot effectively mandatory to continue participation in Israel’s mainstream society.

On Aug. 29, Israeli health officials announced at a press conference that effective Oct. 1, fully vaccinated Green Pass validation status would expire six months after the second dose is received, according to news website Arutz Sheva.”

Additionally, citizens returning from overseas travel who have accepted a third injection will be required to quarantine for only 24 hours after arrival. Those who only have two doses are no longer considered fully vaccinated and will be sequestered for 7 days.

On Aug. 24, Haaretz reported Health Minister Nitan Horowitz as saying in comments given on Channel 13 Television, “This is simply because, in terms of its effectiveness, the vaccine is valid only for a period of five or six months.”

“After about half a year, you have to get a third dose. Otherwise, the vaccine loses its power.”

– Source: Israel Vaccine Passport Now Expires After Six Months, Boosters Required

So according to Israeli’s Health Minister, the vaccine is only beneficial for up to 6 months. After that, you will have to get another. And then, after those 6 months are up, then what? Another? And then another? And another? 2 per year COVID shots, in addition to the yearly flu shot? Do I have that correct?

(And do I need to mention Pfizer’s new venture in supplying – out of the goodness of their hearts, I’m sure – a two-pill-a-day regiment to combat COVID symptoms? Of course it’s about our health and not lining their pockets to make them richer. Of course. Because it’s not like we already have a cheap alternative at treating our symptoms that is curiously being continuously suppressed in the news all to steer our focus on their new, more costly product. That would just be ridiculous…)

5. FDA’s own admission: “While the vaccine may not prevent infection, symptoms or transmission of the virus from person to person – “

The FDA has been caught red-handed removing this particular portion from their Frequently Asked Questions webpage.

On August 31, 2021, I took a screenshot of the following information from the FDA’s own website, under the question:

Q: What safety information did FDA evaluate to authorize the Pfizer-BioNTech COVID-19 Vaccine for emergency use and approve Comirnaty?

Here was their response, as of August 23, 2021:

As you can see, I had to retrieve this information from the wayback machine because strangely enough, on September 1st, 2021 – the very next day after I was able to screenshot this data, the FDA removed this portion from their site.

[https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine-frequently-asked-questions] – (content as of September 14, 2021 shows the latest current update as September 1, 2021]

What could have occurred, within 7 days of their “current content”, to decide to remove this very telling statement? Did new data suggesting that the vaccines do prevent infections, symptoms and transmissions suddenly come out within that very brief time period? Or, more likely, they realized that this statement does not reflect the worldwide pressure to get everyone vaccinated?

Speaking of, even the “president” of the United States is conflicted on if the vaccines work or not.

6. Joe Biden: “The bottom line – we’re going to protect vaccinated workers from unvaccinated coworkers.”

“My job as president is to protect all Americans.

So tonight I’m announcing that the Department of Labor is developing an emergency rule to require all employers with 100 or more employees, that together employ over 80 million workers, to ensure their workforces are fully vaccinated or show a negative test at least once a week.

Some of the biggest companies are already requiring this: United Airlines, Disney, Tyson’s Foods – and even Fox News.

The bottom line – we’re going to protect vaccinated workers from unvaccinated coworkers.”

Source: twitter | @POTUS

Um… isn’t the whole point of getting the vaccine to protect oneself from the “virus”, and in the same vein, the unvaccinated? Why does the vaccinated need protection from the unvaccinated? They are supposedly already protected BECAUSE of the vaccine.

At least, that’s what we were always told from the CDC, FDA, government officials, medical/health authorities, etc. At least, until they decided to flip-flop on their assessment and change their definitions. And at least until new “variants” popped out. … And until they misled the public by removing pertinent information from their own websites. And until… well, you get the point. (maybe)

Then we have Joe Biden’s VP also chiming in with her two cents:

“By vaccinating the unvaccinated, increasing our testing and masking, and protecting the vaccinated, we can end this pandemic. That’s exactly what we are committed to doing.”

Source: twitter | @KamalaHarris

The actual bottom line, they are basically admitting that the vaccine doesn’t work. They’ve already admitted they don’t know how long the vaccines last. Dr. Horowitz mentions no longer than 5-6 months. But for all we know, the vaccines “last” 3 days, if they even work at all. How long have you, personally, gone without COVID (or even the flu/common cold) before and after the vaccine? (If you chose to get one?)

After over 20 months, I’ve gotten sick one time that only lasted 4 days, and even then my symptoms were extremely mild. No flu, no runny nose, just a slight sore throat that went away after 4 days. Meanwhile, I’ve had friends get sick shortly RIGHT AFTER the injection. But, you know, they would’ve been considered “unvaccinated” at that point still…

Which brings me to:

7. “Unvaccinated are filling the hospitals!”

Really…? Hm… well, when you consider who they (CDC/FDA/health agencies) consider as “unvaccinated”, it’s no wonder.

Did you know, anyone who is not considered “fully vaccinated” – meaning, 14 days after their second dose, if it’s a two-dose regiment, or 14 days after a single dose if it’s a single-dose only regiment, is considered either a “partially vaccinated” or an “unvaccinated” person, depending on the honesty of the hospitals to report them?

Trust the Science? CDC Counts People Who Died Within 14 Days of Jab as “Unvaccinated”

To put that more clearly, if you get the second vaccine, and get “COVID” (sick/heart attack/myocarditis/blood clots/flu/etc.) 13 days after the shot, YOU CAN STILL BE CONSIDERED AN UNVACCINATED INDIVIDUAL.

Which goes without saying, but if you are experiencing side effects or illnesses a day or two after the first vaccine – they consider you an unvaccinated person. To think of it a different way, by the time you get the first Pfizer shot (and if you’re diligent in getting the second shot 3 weeks from the first), it will take you 35 days before they consider you a fully vaccinated person. For Moderna, that would be 42 days, again assuming you were diligent in getting your second shot right on time.

So if you get sick at any time during this time period and have to be admitted, the hospitals are allowed to write you up as an unvaccinated/partially vaccinated person.

Another interesting thing to consider, if you did get injected, the hospitals do not have to test you unless you present SEVERE symptoms of “COVID”. So this, obviously, is left up to the specific hospital to determine what is “severe” to them. If you have the flu, tossing and turning, throwing up, shivering, crying in pain, etc. – “Well, it’s not severe enough. It’s obviously not COVID. We don’t have to test them.”

Think this might have something to do with the COVID numbers showing more favorably to the vaccinated cases?

Not to mention that even if the vaccinated individual does get tested, the PCR tests were recommended to use a lower set of cycles for them. …Hm, I’m sure that wouldn’t have anything to do with returning a negative result; thus again, making it seem like the vaccines are working.

But I’m sure the hospital system isn’t that corrupt, right? There’s no way they’d be involved in such deliberate manipulation and misconduct, right? Even though these are all protocols that come from the CDC and other government health agencies…? Surely they just care about our well-being even though there have been studies that prove that in the majority of people natural immunity is by-far superior than shady, no long-term data vaccines, right?

Covid-19 natural immunity compared to vaccine-induced immunity: The definitive summary

“They can’t be lying. They wouldn’t do that. They were just mistaken, is all. They’re following the science. It’s science – science changes, you know. No, no, I’m sure that the government and health/pharma industries that are making a lot of money right now due to side effects from… well, not from the vaccines, obviously – it has to be from something else – I’m sure that they care about us far more than my idiot family members who I’ve lived with for all my life and who have raised me and bought me presents and clothed and fed me.

I mean, just look at everything the government and health agencies and other large corporations has offered me for injecting myself with an experimental vaccine! Beer, donuts, McDonald’s, sports and concert tickets, pizza, marijuana, cash – You all are silly if you don’t think the government wants what’s best for us.

‘Lying’…. pfft.”

So… yeah… I’m just going to direct you back up to number 1, again.

I realize how I may sound on this post. It’s not my intention to sound condescending, and I apologize if that’s how I come off. But in certain times, like what’s going on around us today, if it sounds harsh, maybe it needs to be.

When looking at the situation around us, I find it hard to comprehend that there are still people that believe the official narrative even after everything that’s been presented to us. It almost feels as if the events going on around us are deliberately conceived and obviously created to induce as much unbelievable situations to see how people will respond to it. Perhaps like a test to see how much the governments can get away with and still have people believe them. Sadly, a large group have had the wool pulled over their eyes, and simply go along with the establishment without even thinking about it.

Actually, now that I think about it, maybe this really is their goal. It not only helps them along with their corrupt endeavors, whatever that should be, but it also is a means to employ as many people who still believe their narrative to help them achieve it.

What do you think? Are you thinking? Do you know people who are just following along, without a second thought? Or even worse, indulging in a self-righteous attitude that they’re right and everyone else who doesn’t simply follow this narrative is wrong? Ignoring all of the obvious signs that this is just an agenda set to vaccinate everyone, leading up to controlling every aspect of our lives?

This is happening. The government and health officials continue lying because people still fall for it. If you’re reading this, chances are you already know about the deception and lies that we’re being told to continue forcing this unnecessary vaccine on all of us. I’d say it’s very rare for a person who has already bought into the narrative to read a post exposing the corporations on their lies and manipulation. And if that person does read a post similar to this one, will they contemplate on the information within, or automatically dismiss it as a crazy “conspiracy theory”?

There are truths out there for you. But you need to be willing to accept it.

"It's easier to fool people, than to convince them they have been fooled."
- quote often attributed to Mark Twain

I love you all. Even the ones who haven’t woken up to the scam or who simply don’t believe it. And I know it’s weird to say, but I even love the ones perpetrating the scam. They need it the most. There is something twisted and broken within them, and I literally pray for their soul. I hope in the near future, all of us will realize the actions we’re doing to others, and rise up and grow in truth and compassion, instead of remaining in this state of division.

God bless.

Fact checking is extremely important. I want to reiterate not to take everything at face value; no matter what you read, where you read it from, or who you hear it from. And to be clear, do not rely on “fact checking” websites to give you accurate information either. These are just as likely, (if not even more likely…), to feed false information and false debunking accounts to manipulate the reader. Please take everything into consideration before adhering to a certain narrative – and always keep your mind open to other possibilities.

Fair use disclaimer: Some of the links from this article are provided from different sources/sites to give the reader extra information and cite the sources, but does not necessarily mean that I endorse the contents of the site itself. Additionally, I have tried to provide links to the contents that I used from other sites as an educational and/or entertainment means only; if you feel that any information deserves further citation or request to be clarified, please let me know through the contact page.

Featured image by mohamed Hassan from Pixabay [slightly modified]

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Pfizer-BioNTech/COMIRNATY Vaccine Is Still Under “STUDY” Runs to be Completed at Different Intervals Between 2022-2026

” – known serious risks of myocarditis and pericarditis”

In addition to the many debates and conflicts surrounding the “approval” of the Pfizer/BioNTech/Comirnaty vaccine, there is interesting information to glean from the documents involved surrounding this controversy.

The below documents, some from the FDA’s own website, sheds further light into what seems to be a product still in its experimental/study phase. Some of the revelations are chilling, and doesn’t quite give the reassurance that an “approved” drug of this magnitude is more beneficial to us than what it is purported to be saving us from.

Screenshot of the FDA NEWS RELEASE: FDA Approves First COVID-19 Vaccine
taken on August 31, 2021
[ https://www.fda.gov/news-events/press-announcements/fda-approves-first-covid-19-vaccine ]
Content current as of August 23, 2021

Selected quotes in gray text boxes are from the above document:

“Specifically, in the FDA’s review for approval, the agency analyzed effectiveness data from approximately 20,000 vaccine and 20,000 placebo recipients ages 16 and older who did not have evidence of the COVID-19 virus infection within a week of receiving the second dose. The safety of Comirnaty was evaluated in approximately 22,000 people who received the vaccine and 22,000 people who received a placebo 16 years of age and older.

Based on results from the clinical trial, the vaccine was 91% effective in preventing COVID-19 disease.

More than half of the clinical trial participants were followed for safety outcomes for at least four months after the second dose. Overall, approximately 12,000 recipients have been followed for at least 6 months.

The most commonly reported side effects by those clinical trial participants who received Comirnaty were pain, redness and swelling at the injection site, fatigue, headache, muscle or joint pain, chills, and fever. The vaccine is effective in preventing COVID-19 and potentially serious outcomes including hospitalization and death.”

There are a couple of notes to take away from this document. In the above quote, it doesn’t quite specify how long the clinical trial lasted. Only that more than half of the clinical trial participants were followed for safety outcomes for 4 months after the second dose. It also states that 12,000 of the recipients were followed for at least 6 months.

Both of these numbers (4 and 6) are incredibly low quantities when taking into account pregnant women who are at the beginning of their pregnancy. The length of the clinical trial does not take into account the full 9 months needed to determine a healthy pregnancy, nor does it allow for any time to safely assess the development of the baby once born.

The data in this document also does not include differences between those of the placebo group compared to that of the “vaccine” group. In addition, if we are to only take the 12,000 participants into account, which from the wording of the document seems to allude that these are the recipients of the vaccine, that would still leave 10,000 participants unaccounted for. Just from the amount of vaccine recipients (22,000), this is 45% of their study that the data does not reflect. If we are to include the 22,000 of the participants who received the placebo, the data that was not tracked would rise to 72%.

There is also the challenge of how they determined that the vaccine actually prevented COVID. Were these recipients exposed to someone with COVID or were deliberately inoculated with the disease to see if they would get infected? Many people, myself included, have gone on for more than a year without developing COVID, or at least “COVID symptoms”. Since this data only involved a 4-6 month trial period, how many of us (vaccinated, placebo, or otherwise) can say that we have not contracted COVID during this time-frame either? Is this implying that unless you’re vaccinated, you will most likely get COVID every 4-6 months?

Another consideration to take into account are the many testimonies from well-respected and renowned doctors/scientists/virologists who are adamant in their assessment that these vaccines are unnecessary and instead further harms the immune system rather than help it.

In the same regard, those who are unvaccinated will obviously then not contract any of the possible side effects that are listed in this document as well as the many adverse events that are reported to VAERS. Which leaves one to wonder if the benefits really outweigh the risks of the COVID vaccines.

There is also the slight alteration on a different page of the FDA website that gives further clarification as to the efficacy of the COVID vaccines – which does not reflect that of what many people are influenced to believe:

Under the heading:

Q: What safety information did FDA evaluate to authorize the Pfizer-BioNTech COVID-19 Vaccine for emergency use and approve Comirnaty?

Screenshot of the Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions
taken on August 31, 2021
[ https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine-frequently-asked-questions ]
Content Current as of August 23, 2021

UPDATE on September 6, 2021: Since the FDA website decided to remove this particular section from their FAQ (as of 9/1/2021), here is a screenshot taken from the web archive showing its existence:

“While the vaccine may not prevent infection, symptoms or transmission of the virus from person to person – “

This seems to be the heart of the matter, and although it continues with, “it is effective in preventing hospitalization and death.” it is in direct conflict with what we were led to believe this whole time. Most of the mainstream media, big tech platforms, health agencies, etc. have insisted that vaccines are needed to stop transmission of the virus and to protect those around us. However, this one simple statement defies everything that people were coerced into believing.

And with the last part of the sentence concluding that it prevents hospitalization and death, which even that is debatable when looking at the scope of the situation, it leaves one to wonder why this would not be an option for people to decide to take that risk on their own account. When comparing data of young individuals as well and their extremely low risk of hospitalization and death in the COVID setting, there ARE acknowledged threats when they are injected with the vaccine.

“Additionally, the FDA conducted a rigorous evaluation of the post-authorization safety surveillance data pertaining to myocarditis and pericarditis following administration of the Pfizer-BioNTech COVID-19 Vaccine and has determined that the data demonstrate increased risks, particularly within the seven days following the second dose. The observed risk is higher among males under 40 years of age compared to females and older males. The observed risk is highest in males 12 through 17 years of age. Available data from short-term follow-up suggest that most individuals have had resolution of symptoms. However, some individuals required intensive care support. Information is not yet available about potential long-term health outcomes. The Comirnaty Prescribing Information includes a warning about these risks.”

The FDA is also acknowledging that there are higher risks involved with the Pfizer-BioNTech COVID-19 vaccine and myocarditis and pericarditis, especially in males aged 12-17, and up to age 40.

“Information is not yet available about potential long-term health outcomes.”

“In addition, the FDA is requiring the company to conduct postmarketing studies to further assess the risks of myocarditis and pericarditis following vaccination with Comirnaty. These studies will include an evaluation of long-term outcomes among individuals who develop myocarditis following vaccination with Comirnaty. In addition, although not FDA requirements, the company has committed to additional post-marketing safety studies, including conducting a pregnancy registry study to evaluate pregnancy and infant outcomes after receipt of Comirnaty during pregnancy.”

The document is also stating that the possibility of myocarditis and pericarditis is an accepted issue and will continue to be monitored after the marketing of the Comirnaty vaccine.

And in a rather blunt admission, FDA states on their own website that Comirnaty is not required to evaluate pregnancy and infant outcomes after receipt of Comirnaty during pregnancy. This would explain why the initial trial run was only monitored for 4-6 months. An outline in the BLA (Biologics License Approval) also states that Comirnaty will conduct studies on this group as we see in a later section.

BLA documents state Comirnaty vaccine studies to be conducted for the next several years

Screenshot taken from from the FDA BLA Approval on August 31, 2021
[ https://www.fda.gov/media/151710/download ]
Document dated August 23, 2021

Text below is page 5 of the FDA BLA Approval document

Your deferred pediatric studies required under section 505B(a) of the Federal Food,
Drug, and Cosmetic Act (FDCA) are required postmarketing studies. The status of
these postmarketing studies must be reported according to 21 CFR 601.28 and section
505B(a)(4)(C) of the FDCA. In addition, section 506B of the FDCA and 21 CFR 601.70
require you to report annually on the status of any postmarketing commitments or
required studies or clinical trials.

Label your annual report as an “Annual Status Report of Postmarketing Study
Requirement/Commitments”
and submit it to the FDA each year within 60 calendar
days of the anniversary date of this letter until all Requirements and Commitments
subject to the reporting requirements under section 506B of the FDCA are released or
fulfilled. These required studies are listed below:

1. Deferred pediatric Study C4591001 to evaluate the safety and effectiveness of
COMIRNATY in children 12 years through 15 years of age.

Final Protocol Submission: October 7, 2020

Study Completion: May 31, 2023

Final Report Submission: October 31, 2023

2. Deferred pediatric Study C4591007 to evaluate the safety and effectiveness of
COMIRNATY in infants and children 6 months to <12 years of age.

Final Protocol Submission: February 8, 2021

Study Completion: November 30, 2023

Final Report Submission: May 31, 2024

3. Deferred pediatric Study C4591023 to evaluate the safety and effectiveness of
COMIRNATY in infants <6 months of age.

Final Protocol Submission: January 31, 2022

Study Completion: July 31, 2024

Final Report Submission: October 31, 2024

Submit the protocols to your IND 19736, with a cross-reference letter to this BLA STN
BL 125742 explaining that these protocols were submitted to the IND. Please refer to
the PMR sequential number for each study/clinical trial and the submission number as
shown in this letter.

Submit final study reports to this BLA STN BL 125742. In order for your PREA PMRs to
be considered fulfilled, you must submit and receive approval of an efficacy or a labeling supplement. For administrative purposes, all submissions related to these required
pediatric postmarketing studies must be clearly designated as:

• Required Pediatric Assessment(s)

As the document states, the completion study of Comirnaty postmarketing (after approval) is not due until May 31, 2023 / Novermber 20, 2023 / July 31, 2024 respective of older to lower age groups. There is also another important acronym to consider, which is the IND, which stands for Investigational New Drug.

With this knowledge in hand, it’s important to note that the clinical trial run was monitored for 4-6 months after the second dose on around 55% of the recipients, while the actual “approved” drug still in its investigational/study stages is set to be monitored for 2-3 years. This is a sizeable difference in the amount of time to determine safety and efficacy, especially when considering the many events already reported to VAERS. And according to the Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions page from the FDA website:

Screenshot taken from the FDA Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions
on August 31, 2021
[ https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine-frequently-asked-questions ]
Content current as of August 23, 2021

Q: Are vaccine providers required to report side effects?
A: Providers administering Comirnaty or Pfizer-BioNTech COVID-19 Vaccine must report to the Vaccine Adverse Event Reporting System (VAERS) and to Pfizer the following information associated with the vaccine of which they become aware:
  • Vaccine administration errors whether or not associated with an adverse event
  • Serious adverse events (irrespective of attribution to vaccination)
  • Cases of Multisystem Inflammatory Syndrome
  • Cases of COVID-19 that result in hospitalization or death

Acknowledged myocarditis and pericarditis issues being studied on children

” – known serious risks of myocarditis and pericarditis”

Screenshot taken from from the FDA BLA Approval on August 31, 2021
[ https://www.fda.gov/media/151710/download ]
Document dated August 23, 2021

Text in the gray box below are from pages 6-8 of the FDA BLA Approval documents
[ https://www.fda.gov/media/151710/download ]

We have determined that an analysis of spontaneous postmarketing adverse events
reported under section 505(k)(1) of the FDCA will not be sufficient to assess known
serious risks of myocarditis and pericarditis and identify an unexpected serious risk of
subclinical myocarditis.

Furthermore, the pharmacovigilance system that FDA is required to maintain under
section 505(k)(3) of the FDCA is not sufficient to assess these serious risks.

Therefore, based on appropriate scientific data, we have determined that you are
required to conduct the following studies:

4. Study C4591009, entitled “A Non-Interventional Post-Approval Safety Study of
the Pfizer-BioNTech COVID-19 mRNA Vaccine in the United States,” to evaluate
the occurrence of myocarditis and pericarditis following administration of
COMIRNATY.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: August 31, 2021

Monitoring Report Submission: October 31, 2022

Interim Report Submission: October 31, 2023

Study Completion: June 30, 2025

Final Report Submission: October 31, 2025

5. Study C4591021, entitled “Post Conditional Approval Active Surveillance Study
Among Individuals in Europe Receiving the Pfizer-BioNTech Coronavirus Disease 2019 (COVID-19) Vaccine,” to evaluate the occurrence of myocarditis
and pericarditis following administration of COMIRNATY.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: August 11, 2021

Progress Report Submission: September 30, 2021

Interim Report 1 Submission: March 31, 2022

Interim Report 2 Submission: September 30, 2022

Interim Report 3 Submission: March 31, 2023

Interim Report 4 Submission: September 30, 2023

Interim Report 5 Submission: March 31, 2024

Study Completion: March 31, 2024

Final Report Submission: September 30, 2024

6. Study C4591021 substudy to describe the natural history of myocarditis and
pericarditis following administration of COMIRNATY.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: January 31, 2022

Study Completion: March 31, 2024

Final Report Submission: September 30, 2024

7. Study C4591036, a prospective cohort study with at least 5 years of follow-up for
potential long-term sequelae of myocarditis after vaccination (in collaboration
with Pediatric Heart Network).

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: November 30, 2021

Study Completion: December 31, 2026

Final Report Submission: May 31, 2027

8. Study C4591007 substudy to prospectively assess the incidence of subclinical
myocarditis following administration of the second dose of COMIRNATY in a
subset of participants 5 through 15 years of age.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this assessment according to the following schedule:

Final Protocol Submission: September 30, 2021

Study Completion: November 30, 2023

Final Report Submission: May 31, 2024

9. Study C4591031 substudy to prospectively assess the incidence of subclinical
myocarditis following administration of a third dose of COMIRNATY in a subset of
participants 16 to 30 years of age.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: November 30, 2021

Study Completion: June 30, 2022

Final Report Submission: December 31, 2022

It is interesting that the timing to be considered for approval of these vaccines was only a 4-6 month timeframe, however, known dangers/risks, identified as “serious”, are still allowed to be approved and to be studied for 2+ years.

The document also recognizes that myocarditis and pericarditis is enough of a concern to happen after administration of the Comirnaty vaccine, since it mentions several studies just for this specific adverse event, and to continue to assess these reports.

In addition to all of the substudies to be conducted, there is a study to be initiated on a select group of participants to administer a third dose of the Comirnaty vaccine.

All of this information leads credence to the fact that even though the Comirnaty vaccine has “officially been approved” by the FDA, it is still in the investigational stages and being experimented upon on the public. And it goes without saying, but if myocarditis and pericarditis (on top of other reported side effects) are serious risks especially in children (“The observed risk is highest in males 12 through 17 years of age.”), then for this known risk to be offered to infants/toddlers defies any ethically moral boundaries and is in direct violations of the Nuremberg Code.

The next section also provides further evidence that there have been NO studies in the safety/efficacy of the Pfizer-BioNTech/Comirnaty vaccine on pregnant women.

Pregnancy/Births were not studied during the initial Pfizer-BioNTech/Comirnaty trial runs

Another snippet from the FDA Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions website page, states the following:

Screenshot taken from the FDA Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions
on August 31, 2021
[ https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine-frequently-asked-questions ]
Content current as of August 23, 2021

Q: Can pregnant or breastfeeding women receive the Comirnaty or Pfizer-BioNTech COVID-19 Vaccine?

A: While there have been no specific studies in these groups, there is no contraindication to receipt of the vaccine for pregnant or breastfeeding women. Pregnant or breastfeeding women should discuss potential benefits and risks of vaccination with their healthcare provider.

The acknowledgement above seems to indicate that the FDA and Pfizer-BioNTech/Comirnaty company have side-stepped this particular group in their vaccine studies, and have left it up to the healthcare provider to determine whether or not to administer this vaccine to pregnant women or women who are breastfeeding. This alone should be enough of a statement that there is no sufficient/professional data to analyze if the Comirnaty is safe during pregnancies/breastfeeding stages.

And if one were to consider the VAERS reporting system, in which the Pfizer-BioNTech company is required to report to, there have been numerous conditions of miscarriages/stillbirths/complications during pregnancy after administration of the COVID vaccine. While it is difficult to determine if these complications were a direct result of the vaccine, it is up to the scientific/healthcare community to investigate these cases in a thorough, unbiased and uninfluenced manner.

Another extremely alarming section of the FDA BLA Approval documents shows the following trial to be monitored in pregnant women:

Screenshot taken from from the FDA BLA Approval on August 31, 2021
[ https://www.fda.gov/media/151710/download ]
Document dated August 23, 2021

Text in the gray box below are from pages 9-10 of the FDA BLA Approval documents
[ https://www.fda.gov/media/151710/download ]
POSTMARKETING COMMITMENTS SUBJECT TO REPORTING REQUIREMENTS
UNDER SECTION 506B

We acknowledge your written commitments as described in your letter of August 21, 2021 as outlined below:

10. Study C4591022, entitled “Pfizer-BioNTech COVID-19 Vaccine Exposure during
Pregnancy: A Non-Interventional Post-Approval Safety Study of Pregnancy and
Infant Outcomes in the Organization of Teratology Information Specialists
(OTIS)/MotherToBaby Pregnancy Registry.”

Final Protocol Submission: July 1, 2021

Study Completion: June 30, 2025

Final Report Submission: December 31, 2025

There are a couple of key takeaways in this section that are of incredible importance. One major term to focus on is the word “NON-INTERVENTIONAL“.

According to What is a Non Interventional Study?, “In general, a non interventional study (NIS) (also called a non interventional trial) is where a patient takes regular medicine, prescribed according to the label. In an NIS, the researcher sets out to exert as little influence as possible on the patient’s condition while studying a medicine’s “…effectiveness, safety and tolerability under real life conditions” (Mishra & Vora, 2010).”

The article also reiterates multiple times that “non-interventional” studies are observational studies – the researchers are not to interfere with the dosages in any way but to prescribe them exactly as listed on the label. It also seems to imply that even if severe side effects show up, they are to still carry through with the “medicinal product” in that patient as prescribed. Another insinuation that one can make is that in order to not interfere with the study, it is not recommended to prescribe treatments that may help alleviate potential side effects. The term “tolerability” is implying to keep the patient going through the side effects in order to continue to study the long-term effects of the investigational new drug.

However, with the inclusion of “real life conditions”, it doesn’t indicate whether the patient can seek out physicians to investigate what is causing the side effects in their system and engage in therapeutic treatments to alleviate these effects. If a study is to be conducted in real life conditions, then it is to be expected that patients will seek treatments on their own while the researcher is only required to observe the patient to see how the alternative treatments interact with the drug/symptoms.

The same article goes on to state that the UK/EU have different definitions of what “non-interventional” means. “Aronson (2004) states… “the term ‘non-interventional’ in the Directive doesn’t mean non-interventional (i.e. non-interference) at all; it refers to an intervention with a licensed medicinal product.”

There is controversy and conflicts in this statement as another article, Interventional or Non-Interventional? Analyzing the Differences Between Clinical Studies Using Medicines in the European Union points out:

“Although defined in DIR 2001/20/EC, non-interventional studies are outside its scope. Due to the lack of harmonized regulation, some studies designed to be non‑interventional may be considered clinical trials by EU authorities. The two blinded studies described in Table 4 (see PDF) were considered clinical trials in the EU for planning on collection of data to support the marketing authorization application of experimental IMPs, despite no IMP being given and normal clinical practice being kept during the study period. Sponsors are thus advised to consult with authorities when planning studies under these conditions and/or whenever the objectives or design may raise questions.”

Further in the article, it states the following, which again, is not reassuring considering the policies/guidelines/mandates that authorities have been engaging in in order to mandate these investigational new drugs (COVID vaccines) onto the public:

“There is no centralized submission procedure for non-interventional studies with the exception of non-interventional PASSs, imposed as an obligation by an EU competent authority.{9} Because non-interventional studies do not have harmonized legislation, some Member States require submissions to regulatory authorities, while others do not. It is therefore important that sponsors are familiar with the regulatory framework of target EU Member States, and that they consult with local competent authorities and ethics committees (ECs) when justified.”

It’s sad to have to point this out, but the quote does specify “competent” authorities. And even the inclusion of “ethics committees” is not comforting seeing as how one of the leading figures in ethics study is Christine Grady, Chief of the Department of Bioethics at the National Institutes of Health Clinical Center, and wife of Anthony Fauci – Director of the National Institute of Allergy and Infectious Diseases and Chief Medical Advisor to the president, and who is also a large spokesperson for the experimental injections.

The other takeaway from section 10 of the FDA BLA documents is the term “TERATOLOGY“.

Definition of teratology
: the study of malformations or serious deviations from the normal type in developing organisms
merriam-webster/teratology

Teratology, branch of the biological sciences dealing with the causes, development, description, and classification of congenital malformations in plants and animals and with the experimental production, in some instances, of these malformations. Congenital malformations arise from interruption in the early development of the organism. Malformations in human infants, for example, may occur because the infant’s genotype contains mutant genes or includes an abnormal number of chromosomes; they also may occur if early in pregnancy the mother has had German measles (rubella), has taken some injurious drug, or has been exposed to an injurious dosage of radiation. Experimental studies suggest similar types of factors can cause malformations in animals and plants.”
britannica/teratology

Now when you combine the terms “non-interventional” and “teratology” together, it is suggesting that the ongoing studies (that were not conducted to begin with even in a clinical trial setting, as per the FDA’s own response) on pregnant women with Comirnaty and on the developing baby, will be monitored with as little intervention as possible and is mostly to be observed for malformations/genetic defects/miscarriages/etc.

In other words, safety and efficacy were never studied in this particular group, and neither was it studied in infants. It has also not been studied for long-term analysis, as the 4-6 month trial runs proves. The current “approval” it is undergoing now is an authorized experiment on the human population that is posing incredibly unnecessary risks when considering the many effective treatments that are already available to combat respiratory illnesses. And the insistent assertiveness to push this “investigational new drug” onto babies/children who are at extremely low risk for this illness is a disastrous decision from those in an “authoritative” position and should be investigated for malfeasance and misconduct.

This is also not the first time that government agencies/health industries/etc. have conducted experiments on the public.

The Tuskegee/Syphilis experiment was initiated onto a selection of African American men between 1932-1972. The study was only stopped (allegedly) after a publication was released on Associated Press in 1972 about the immorally unethical experiments being conducted on this group:

“Of about 600 Alabama black men who originally took part in the study, 200 or so were allowed to suffer the disease and its side effects without treatment, even after penicillin was discovered as a cure for syphilis. Treatment then probably could have saved or helped many of the experiment participants, PHS officials say.”AP WAS THERE: Black men untreated in Tuskegee Syphilis Study

This study seems to echo the sentiments we see going on with the coronavirus situation, in which only one type of drug is being promoted (the COVID vaccines) while suppression of other treatments that have been proven to work (such as Ivermectin) has been denounced by the very same government/health/medical fields that have conducted these experimental studies.

A study that involved the CDC/FDA’s approval, this time on Black and Latino babies, was conducted in the early 1990’s and involved the measles vaccine:

“1990: CDC Inoculated Black and Latino Babies with an Unlicensed Measles Vaccine
A covert clinical trial by the Center for Disease Control (CDC) and Kaiser Permanente inoculated Black and Latino babies with an experimental measles vaccine without informing parents the vaccine was experimental. More than 1500 six-month old black and Hispanic babies in Los Angeles are given the deadly “experimental” measles vaccine that had never been licensed for use in the United States; a vaccine that had been tested in African and Mexican babies resulting in high death rates. The parents were never informed and they never gave their consent. The CDC harmed babies, violated federal law, and trampled on parental rights with impunity.”
1990 FDA Issued a Waiver From Consent; Covert CDC Experimental Vaccine Test on Black / Latino Babies

It’s interesting that the measles vaccine experiment identifies Kaiser Permanente specifically, because as we see in another section of the FDA BLA Approval for Comirnaty, it seems as if Kaiser Permanente makes another appearance in the role of human experimentation:

Text in the gray box below is from page 10 of the FDA BLA Approval documents
[ https://www.fda.gov/media/151710/download ]

13. Study C4591014, entitled “Pfizer-BioNTech COVID-19 BNT162b2 Vaccine
Effectiveness Study – Kaiser Permanente Southern California.”

Final Protocol Submission: March 22, 2021

Study Completion: December 31, 2022

Final Report Submission: June 30, 2023

It would seem that the approval by the FDA of these IND drugs (Pfizer-BioNTech/Comirnaty vaccine) is a way for the government/health agencies to skirt away from liability by stating that since the vaccines are no longer “experimental” by their definition, and that they are FDA “approved”, it is no longer required to gain informed consent of these drugs. In addition, as to the technicality of their terms and protocols, there are a multitude of ways to interpret their “informed consent” rules, which officials can then bend or define in any way that best reflects the use of their study/drug.

[ https://www.fda.gov/regulatory-information/search-fda-guidance-documents/informed-consent#exceptions ]

Also keeping in mind how long it was determined before the “health agencies” granted approval of the Pfizer-BioNTech/Comirnaty vaccine – (4-6 months) – it would be conclusive to state that the vaccines have NOT sufficiently been studied in young children or pregnant women (or even the rest of the age groups because of the short amount of time the clinical trial study was conducted in), and the subsequent approval of this vaccine is to continue this research on the population who is exceedingly being pressured into taking this investigational new drug.

There is also the matter of the many adverse events that have been reported since the inoculation of these injections, that have largely gone unheeded within the health/medical institutions that are endorsing this drug. Other than the widely acknowledged myocarditis and pericarditis, most common in young males, which is still being studied and allowed to persist onto the public.

So again, taking into account the collusion of the government/health/medical/research fields to conduct experiments on the public, it would be necessary to reflect upon these agencies for additional breaches upon human rights, consent, and ethical behavior.

Fair use disclaimer: Some of the links from this article are provided from different sources/sites to give the reader extra information and cite the sources, but does not necessarily mean that I endorse the contents of the site itself. Additionally, I have tried to provide links to the contents that I used from other sites as an educational and/or entertainment means only; if you feel that any information deserves further citation or request to be clarified, please let me know through the contact page.

Featured image by Ahmad Ardity from Pixabay

Might COVID Injections Reduce Lifespan?

“Yeadon, Montagnier, Zelenko and others are raising concerns about global genocide.”

All Global Research articles can be read in 51 languages by activating the “Translate Website” drop down menu on the top banner of our home page (Desktop version).

Visit and follow us on Instagram at @crg_globalresearch.

***

Evidence suggests people who have received the COVID “vaccine” may have a reduced lifespan as a result of the acute, subacute and long-term effects from the COVID injection

If you’ve gotten the COVID shot, consider yourself high risk for COVID and implement a daily prophylaxis protocol. This means optimizing your metabolic flexibility, vitamin D, and taking vitamin C, zinc and a zinc ionophore on a daily basis, at least throughout cold and flu season

Evidence shows NAC may be used to prevent blood clots and break up any that might already have formed

If you’re low risk for COVID and have not been vaccinated, make sure you have these items on hand and begin treating at the very first signs of cold or flu symptoms

Also buy yourself a tabletop jet nebulizer, some saline solution and food grade hydrogen peroxide. Nebulized peroxide is an excellent go-to both for prevention and treatment, regardless of the stage the respiratory infection is in. For prevention, nebulize every other day. For treatment, use at first signs of respiratory infection

*

Watch the video here.

In this interview, return guest Dr. Vladimir Zelenko discusses an incredibly serious concern, one shared with at least two other highly credible experts — Michael Yeadon, Ph.D., a life science researcher and former vice-president and chief scientist of allergy and respiratory research at Pfizer, and professor Luc Montagnier, a world-renowned virologist who won the Nobel prize for his discovery of HIV.

Yeadon, Montagnier and Zelenko all believe the COVID-19 shots could reduce life expectancy by several decades, depending on several factors, including whether you’re required to get booster shots. In fact, there may be reason to suspect that many who get the jabs and subsequent boosters could lose their lives within two to three years, as a result of pathogenic priming.1,2

Many may not realize that when I was a youngster I was a Boy Scout, but you might know their motto is “Be Prepared.” It is an approach that has served me well over the years. I am not stating unequivocally that dire outcome will materialize, as my interview next week with Dr. Peter McCullough goes into. However, it would seem prudent to have a good protocol in your hands in anticipation of a worst-case scenario.

So, on that note, Zelenko and I take a deep dive into what can be done to prevent such a fate. Zelenko categorizes the risks of COVID-19 “vaccines” into three categories: acute, subacute and long-term, so let’s begin by reviewing the primary risks found in each of these categories.

Risk Category No. 1 — Acute Risks

The acute phase of harm begins at the moment of injection and likely lasts for about three months or so. Based on reports filed with the U.S. Vaccine Adverse Event Reporting System (VAERS), it’s clear that many cannot survive past the acute phase.

About 6,000 deaths have been reported so far, and death commonly occurs within 48 hours of injection. Many serious disabling events also occur rather rapidly, typically within a few days or weeks. However, Zelenko has a very dismal perspective on the accuracy of the VAERS database. He explains:

“According to a paper published by the Salk Institute in San Diego, they’ve discovered that the spike protein that’s generated through the vaccination itself has negative health effects. It’s toxic … on its own …

There’s plenty of evidence that shows that it spreads from the injection site and goes to the bloodstream, and basically comes into every single cell in the body.3,4

mRNA has a half-life of around one to two weeks, depending on the mRNA, and during that interim, each mRNA molecule makes around 2,000 to 5,000 spike proteins. So, we’re talking about trillions and trillions of spike proteins.

Your entire body becomes a spike protein factory. Several orders of magnitude more than if you were to get COVID, because COVID infects the upper and lower airways primarily. Those are the cells that get infected and begin to produce spike proteins. But here we’re injecting the vaccine and it actually travels to every single cell in your body and converts every single cell in your body into a factory for spike proteins.”

As the mRNA disseminates through your vascular system, the cells lining your blood vessels begin producing spike protein. This is why we’re seeing such a staggering number of reports of people experiencing blood clots from these injections.

According to Zelenko, 40% of these events occur within the first two days after injection. The risk then diminishes, but vascular events such as heart attacks, strokes, renal infarcts and pulmonary infarcts don’t completely peter out until about three months after the last injection.

But these events of the past three months are not being reported to VAERS. It is, of course, possible that people simply aren’t connecting them to the COVID shot they got several months earlier.

How Many Have Actually Died From the COVID Shots?

As noted by Zelenko, underreporting is part of the problem we’re facing. The real number of side effects is impossible to determine, given the fact that the Food and Drug Administration didn’t insist on a robust post-vaccination data collection system, but it’s most certainly higher than what VAERS is listing.

“If you look at the VAERS [vaccine adverse event reporting system], which in my opinion is a piece of garbage … as of today, let’s say says there’s 6,000 deaths associated with taking the vaccine. Well, we need to understand what that actually means,” Zelenko says.

“If you look at the 2009 Harvard study on the VAERS system, they said only 1% of events are actually reported. So, OK … whatever the number is, it’s not 6,000. Maybe only 10% are being reported. I don’t know. But definitely it’s being underreported.

And then there’s two [additional] big problems. There’s evidence coming out that VAERS reports that have been filed are being erased off the server, No. 1. No. 2, I personally know of two dozen cases of deaths associated with the vaccine, and the doctor and/or family members that tried to file a VAERS report, their reports were rejected due to some technicality.

The fact that they all couldn’t make a report, that raises my eyebrows. What percentage of the information are we actually seeing? The answer is, I estimate, there are already around 200,000 dead Americans, directly related to the vaccinations.”

To get to that number, Zelenko assumes only 10%5 of adverse effects are reported. Studies have indicated it could be as low as 1%.6,7 That gives us a death toll of about 60,000, to which he adds another 140,000 given the fact that reports are being scrubbed and refused.

“The point is that it should definitely raise eyebrows and have the public start screaming and saying, ‘We want to know the truth. We want to know the accurate numbers. Stop suppressing the truth … I want to be able to make an informed choice whether or not I want to take this injection.’ And that’s not being given to the people.

My problem is not with the vaccine. My problem is with the government, governing bodies and certain people that are obstructing the flow of life saving information and suppressing the truth from people, and then using coercion to force people to take this vaccine. That’s the nefarious part.

The suppression is so blatant and so overt that doctors with impeccable credentials are being deplatformed for just voicing an opinion. And then you couple that together with proven prehospital treatment approaches and protocols that have been proven to reduce hospitalization and death by 85%, and that information is being suppressed.

So here you have a dual censorship where the positive, hopeful, life-saving information is being suppressed and the dangerous outcomes of the vaccination approach is being suppressed. It’s a perfect setup for genocide.”

Risk Category No. 2 — Subacute Risks

The subacute risk phase, which begins around three months’ post-injection, is exceedingly difficult to quantify. At bare minimum, it’s likely to last several months to a couple of years. The primary concern now is antibody-dependent enhancement (ADE), also referred to as pathogenic priming and/or paradoxical immune enhancement (PIE) as it more accurately describes the disease mechanism.

Zelenko believes the mRNA will have degraded by this time, and your cells will hopefully no longer produce spike protein. I believe he may be overly optimistic here, as the synthetic mRNA has been genetically modified to be less perishable, plus it’s encased in a nanolipid to resist breakdown.

I suspect this modified mRNA may remain viable far longer than anyone suspects, thanks to its synthetic nature. What’s more, there’s a mechanism by which the mRNA can be reverse transcribed into your DNA, which would make the spike protein production permanent — and probably intergenerational. I describe this process in “The Many Ways in Which COVID Vaccines May Harm Your Health.”

If Zelenko is correct, then the primary disease agent now switches from the spike protein to the antibodies produced in response to the spike protein. We don’t know how long these antibodies will last, but chances are they’ll stick around for a number of months or years.

While antibody production is the primary purpose of these shots, and the response said to provide you an immune benefit, they can actually be the source of problems.

Animal trials in which conventional coronavirus vaccines were tested have shown coronavirus vaccines routinely cause ADE,8,9,10,11,12 so when the animals are challenged with the real virus they’ve been immunized against, they can get seriously ill and even die. If hospitals start filling up with vaccinated individuals this fall, you’ll know why. They’re suffering the effects of ADE.

“In other words, those antibodies that were produced with the vaccination were pathologic,” Zelenko says. “They were lethal and they led to an exaggerated immune response. That’s what it means, antibody-dependent enhancement. It’s an enhancement of your immune response in a way that it will kill you …

The question is, how safe is it long-term, or in the subacute [phase] from three months to three years? That is a big question mark. Based on animal models — and this is what Dr. Mike Yeadon is saying — it could be absolutely genocidal. It’s the biggest gamble on the survival of humanity in the history of humanity.”

However, as a counter to this view, Dr. Peter McCullough, who is in complete agreement with the engineering of this event and it being one of the most egregious crimes against humanity, is not convinced that there will be a massive die-off in the fall.

He is well-trained in the science and has essentially completed a fellowship in COVID-19 along with being the senior editor of two prestigious medical journals so his opinion also deserves consideration. We will be posting his interview next Sunday, July 11, 2021.

Why Is Humanity’s Survival Being Risked?

The questions on many people’s mind right now are, “Why are lifesaving early treatment approaches suppressed?” “Why are the toxic side effects and death rates of the vaccines being suppressed?” and “Why are entire continents being coerced into taking a vaccine that is both medically unnecessary and unproven in terms of safety and effectiveness?”

Taken together, none of it makes any sense, which is why people like Yeadon, Montagnier, Zelenko and others are raising concerns about global genocide. Is that what this is all about? Is there an alternative interpretation of what’s happening? When you consider the actual data, mass vaccination simply isn’t necessary, so why the frantic push to get a needle in every arm? Zelenko explains:

“There’s something called medical necessity. So, let’s analyze if there’s any medical necessity for this vaccine, and you have to do that in a systematic way based on demographics.

If you look at the CDC’s data, anyone 18 and younger has a 99.998% chance of recovery from COVID-19 with no treatment. [Their risk of dying is] 1 in a million. It’s safer than influenza virus. If you gave me a choice, I would rather my kids have COVID-19 than influenza. So, why would I immunize a demographic that has close to 100% chance of recovery with an experimental vaccine that has already killed more kids than the virus?

If you look at the demographic between 18 and 45, people who are healthy have a 99.95% chance of recovery with no treatment … according to the CDC. Same question, why would I vaccinate a demographic that recovers on its own with no treatment?

Third question, if someone has antibodies — and there’s a plethora of evidence [showing] naturally produced antibodies are much more effective in clearing future viruses than vaccine-induced antibodies … Natural immunity is much better, more effective and safer, than vaccine-induced immunity. So, someone who has antibodies already from having COVID before, why would I vaccinate them? …

Fear is an extremely useful tool in manipulating the behavior of people. And that fear has been used to create a psychological motivation to get vaccinated with a vaccine that, in my opinion, has no medical necessity, has tremendous amount of actual and potential risks, and very questionable efficacy.”

Risk Category No. 3 — Long-Term Risks

Beyond the two-to three-year mark are the long-term risks, which are even more difficult to predict. One particularly difficult risk to predict or quantify is infertility. It’ll take decades before we have the data on reproductive effects. Women in their 20s who get the jab might not get serious about trying to get pregnant until they’re in their 30s.

Teens and young children will have to wait decades before fertility can be ascertained. Of course, by then, it’ll be too late. The damage will be done, and hundreds of millions will be in the same boat.

Zelenko cites research published in The New England Journal of Medicine, which concluded COVID vaccination during pregnancy had no increased risk of miscarriage. However, a closer look at the data set revealed that this was only true for women who got vaccinated during their third trimester. Women who get the COVID jab in their first and second trimester have a 24-fold higher risk of miscarriage.

There are also reports of declining sperm counts and testicular swelling in men, and menstrual cycle disruptions in women of all ages. “There is an absolute effect on fertility,” Zelenko says. We just don’t know to what degree yet.

Overall life expectancy is likely to be affected across the board but, again, it’s very difficult to predict just how many years or decades will be lost. Zelenko, like many other doctors, suspect autoimmune diseases and cancer rates will go up as a result of the jabs. As noted by Zelenko:

“Whether you look at the acute spike protein-induced death, the miscarriages, or the myocarditis in young adults, or you look at the subacute pathogenic priming issue, or you look at the potential long-term effects of infertility, auto immune disease and cancer, you have an absolute setup for a genocide. And that’s why these world-leading thought leaders, scientists, are cautioning people …

Let’s do a thought experiment. If COVID-19 were to infect every single human being on this planet and was not to be treated, what would be the overall global death rate? The answer is less than 1%, and I’m not advocating for that, by the way. That’s a lot of people still.

Now, what is going to be the death rate from global vaccination? That is going to be several orders of magnitude greater. And it actually depends how far out you look. Because if someone’s meant to live 80 years and they live 60 years, how do you quantify that? …

We’re talking about 1.5 to 2 billion people [dying] for no reason, except the agendas of a few psychopaths or sociopaths. Why do I say that? It’s because there have been people advocating for population reduction for decades. I just saw a video from [U.K. prime minister] Boris Johnson’s father … advocating for the reduction of England’s population to 15 million …

This type of ideology exists. In this generation, it’s not really anti-Semitic. What it is, is there’s a small group of sociopaths that believe … they’ve evolved into a superhuman enlightened [state] that entitles them the right to dictate the course of history.

For example, Bill Gates in 2015 said the world population needs to be reduced by a certain percentage because of global warming or whatever. So, my question is a very simple question. He’s one of the main supporters and profiteers of global vaccination. Why would I take a vaccine for my health from someone is advocating for the reduction of the world population?

Another scary individual is Klaus Schwab, the founder of the World Economic Forum. He’s very influential. He wrote the book ‘COVID-19 The Great Reset.’ In 2016, in a French interview … Schwab made an announcement that within 10 years, all of humanity will be tagged with an identifier. If you look at the UN 2030 plan, which was crafted by the World Economic Forum, it says ‘America will no longer be a superpower.’

That’s a stated agenda. Then, my favorite is, ‘You’ll own nothing and you’ll be happy. You won’t eat any meat. Fossil fuels will be prohibited. There’ll be a billion refugees, which will have to be integrated into your societies.’ So, my question is, what sociopath feels entitled to make a statement like ‘You will own nothing and you will be happy’?

What entitles this type of individual, or group of individuals, to think that way? Well, they believe that they’re enlightened far beyond the average human or subhuman.”

War Against God

Zelenko, a devout Jew, believes the root of this global takeover is really a war against God. The implication is that life has sanctity, and if life has sanctity, we have human rights, “earned” by our birth alone. This is the source of natural law. And, if we have human rights, handed down by God, then no one has the right to decide how long any one of us should live, or how many people there should be on the planet.

“That’s God’s prerogative,” Zelenko says. “However, if you take that out and view people as no different than an animal, a Darwinist perspective or eugenics perspective, and basically survival of the fittest is the yardstick that you measure the dominance hierarchy of humanity, in that case, these people feel that they are on top of the pyramid, and that entitles them to decide if you and me should live …

I call the [COVID] vaccine ‘Zyklon-V.’ That is the gas the Nazis used to kill my relatives. So to express my sentiments, I call it Zyklon-V. It’s an absolute weapon of mass destruction. People are being lied to, and they’re running into the gas chambers themselves because of the pathogenic fear.”

How to Protect Your Health Post-Jab

If you or someone you know or love got the COVID jab and now have serious regrets, there are definite strategies you can use to protect your health.

It appears if you made it through the first three months OK, then your risk for blood clots is likely radically diminished. To counteract excessive clotting, an anticoagulant may be appropriate. A natural alternative with great promise is n-acetyl cysteine (NAC), as it has both anticoagulant13 and thrombolytic effects,14 meaning it may both prevent clots and break up clots that have already formed. Obviously, do not get any more booster shots.

In the subacute phase, your No. 1 goal will be to avoid ADE. The key to this is to avoid triggering a pathogenic immune reaction, and the only way to do that is to implement some sort of prophylactic protocol, i.e., a COVID, common cold and influenza prevention protocol.

This is especially important for anyone that has received the COVID jab as they are at a high risk of having complications and are under the false impression that they are “protected” when actually they are at increased risk now that they got the jab and need to take extraordinary precautions.

Any symptoms of upper respiratory infection should also be treated immediately, not later. COVID is a multi-phase disease. The first phase is the viral phase, which lasts five to seven days. This is when it’s most easily treated. After Day 7, the disease typically progresses into the inflammatory phase, which requires different treatment.

Zinc supplementation is an important component for prevention and early treatment in the viral stage, as it impairs viral replication. You need to take it with a zinc ionophore, however, such as quercetin, EGCG (green tea extract), hydroxychloroquine or ivermectin.

“The majority of the COVID protocols focus on inhibition of our RNA virus replication. What that means is that for a virus to make copies of itself, it needs to enter the human cell. In the case of RNA viruses, all the COVID, coronaviruses and even the influenza viruses, they use a common pathway called RNA dependent RNA polymerase. That’s a very important enzyme.

That enzyme is what makes copies of the viral genetic material, which then enables for new viruses to be formed and spread. So, if you inhibit the viral RNA replication process, you’ll eliminate viral spreading, viral growth. The beautiful thing about what we found with zinc is that zinc inhibits this enzyme extremely well, if there’s another zinc [molecule] inside the cell.

But zinc cannot really get into the cell on its own. That’s where the concept of zinc ionophores come in. Zinc ionophores opens the door in the cell membrane and allows for zinc to go from outside of the cell, to inside of the cell. And when you increase the concentration of zinc inside the cell, then it can effectively inhibit this enzyme, stopping most if not all, coronaviruses and influenza viruses from replicating.”

If you want to use either hydroxychloroquine or ivermectin and live in a state that restricts their use, look for online telehealth options. The American Frontline Doctors is one resource. They only charge $90 for a consultation and you will be able to get the prescription that you need. Do not use Ivermectin from veterinary sources as it may be contaminated and is not designed for human use.

In addition to zinc and a zinc ionophore, you also need to optimize your vitamin D level. The range you’re looking for is 60 ng/mL to 80 ng/mL year-round. The appropriate dose of oral vitamin D3 is the dose that gets you within that range.

Vitamin C is another important component, especially if you’re taking quercetin, as they have synergistic effects. To effectively act as a zinc ionophore, the quercetin needs vitamin C.

In an effort to make it easier for patients, Zelenko has developed an oral supplement that contains all four: vitamin C, quercetin, vitamin D3 and zinc. It’s called Z-Stack and can be purchased on zstacklife.com. For a downloadable “cheat sheet” of Zelenko’s protocol for COVID-19, visit VladimirZelenkoMD.com

The take-home message here is that if you’ve gotten the jab, consider yourself high risk for COVID and implement a daily prophylaxis protocol. This means optimizing your vitamin D, and taking vitamin C, zinc and a zinc ionophore on a daily basis, at least throughout cold and flu season.

It would also be useful to do a daily sauna. Ideally one that can heat up to 170 degrees Fahrenheit. The best saunas are far-infrared and have low EMFs. Sadly, I don’t know any that go to 170 degrees and are low EMF.

I use one that goes to 170 and then I turn it off and turn on the SaunaSpace four near IR bulb system in the sauna and go in for 20 minutes. This practice activates heat shock proteins which will help remove the spike proteins and improve other damaged proteins in your body.

If you’re low risk for COVID and have not been vaccinated, make sure you have these items on hand and begin treating at the very first signs of cold or flu symptoms.

Nebulized Peroxide and Other Health Promoting Measures

In addition to NAC (to prevent and break up clots), vitamin D, vitamin C, quercetin and zinc, buy yourself a tabletop jet nebulizer, some saline solution and food grade hydrogen peroxide. You’ll want to dilute the peroxide with saline to get a 0.1% solution.

Due to risks to my personal safety we had to remove the nebulized peroxide videos from the site but they are now up on our sustack site and you can view all of them here

hydrogen peroxide dilution chart

Nebulized peroxide is my personal go-to both for prevention and treatment, regardless of the stage the respiratory infection is in. To learn more, download Dr. Thomas Levy’s free e-book, “Rapid Virus Recovery.” As a preventive measure, simply nebulize every other day. Vitamin C is important here too, as it works as a catalyst for the peroxide. A daily dose of 500 milligrams would likely be sufficient for most.

We were forced to remove all the hydrogen peroxide videos that I had previously posted for liability reasons but fortunately they are all now posted on our Substack site. This is important as, in my view, this is the most important step you can take. I would recommend nebulizing a 0.1% solution every day as indicated in the videos, linked below.

There is no danger in doing it every day and likely there is a health benefit. As Dr. Tom Levy describes in one of the videos below, it seems to help improve your bowel movements, which may be a result of eliminating respiratory pathogens that were having negative impact on your microbiome.

Other important health-preserving strategies include the following:

  • Make sure you’re metabolically flexible so that your body can seamlessly transition between burning fat and sugar as your primary fuel. This will allow your innate immune system to function optimally. Time-restricted eating is one surefire way to accomplish this.
  • Avoid processed seed oils in your diet, such as sunflower oil, corn oil, safflower oil or avocado oils. All contain high levels of linoleic acid, which impairs your mitochondrial function, and in upper respiratory infections, it’s the precursor for the Leukotoxin that occurs in these infections.
  • Focus on certified-organic foods to minimize your glyphosate exposure, and include plenty of sulfur-rich foods to keep your mitochondria and lysosomes healthy. Both are important for the clearing of cellular debris, including these spike proteins. You can also boost your sulfate by taking Epsom salt baths.
  • To combat the toxicity of the spike protein, you’ll want to optimize autophagy, as this may help digest and remove the spike proteins. Time-restricted eating will upregulate autophagy, while sauna therapy, which upregulates heat shock proteins, will help refold misfolded proteins. They also tag damaged proteins and target them for removal.

It is important that your sauna is hot enough (around 170 degrees Fahrenheit) and does not have high magnetic or electric fields.

  • If you’re having post-vaccination symptoms, you could consider:

Low-dose interferons such as Paximune, to stimulate your immune system

  • Peptide T (an HIV entry inhibitor derived from the HIV envelope protein gp120; it blocks binding and infection of viruses that use the CCR5 receptor to infect cells)
  • Cannabis, to strengthen Type I interferon pathways, which are part of your first line of defense against pathogens
  • Dimethylglycine or betaine (trimethylglycine) to enhance methylation, thereby suppressing latent viruses
  • Silymarin or milk thistle to help cleanse your liver

The National Vaccine Information Center (NVIC) recently posted more than 50 video presentations from the pay-for-view Fifth International Public Conference on Vaccination held online October 16 to 18, 2020, and made them available to everyone for free.

The conference’s theme was “Protecting Health and Autonomy in the 21st Century” and it featured physicians, scientists and other health professionals, human rights activists, faith community leaders, constitutional and civil rights attorneys, authors and parents of vaccine injured children talking about vaccine science, policy, law and ethics and infectious diseases, including coronavirus and COVID-19 vaccines.

In December 2020, a U.K. company published false and misleading information about NVIC and its conference, which prompted NVIC to open up the whole conference for free viewing. The conference has everything you need to educate yourself and protect your personal freedoms and liberties with respect to your health.

Don’t miss out on this incredible opportunity. I was a speaker at this empowering conference and urge you to watch these video presentations before they’re censored and taken away by the technocratic elite.

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