Studies PROVE That Live Parasites and Parasite Proteins Are Being Used/Tested in Vaccines | Are Parasites the Cause of ALL Illnesses?

At least 650,000 – 800,000 CHILDREN have been injected with a malaria vaccine to test its efficacy.

After investigating parasitic like organisms possibly being used in vaccines – I realized, these studies have been conducted for a LONG TIME. And who knows for how long?

It is a true, real, honest-to-badness endeavor.

Now, a lot of scientists/doctors/virologists/biologists may already know all of this and see nothing wrong with it. I, however, an innocent researcher, never knew that this was a real agenda all in the sake of “curing” people from… well, parasites.

I know. It doesn’t make sense to me – why inoculate someone with parasites, if they are trying to prevent them from the very same parasite they’re being inoculated with?

It reminds me of the flu/COVID shots, actually. Why deliberately inoculate someone with a virus that you’re trying to prevent/immunize them from getting? Especially if they have a chance of acquiring it naturally and producing the more beneficial ‘natural immunity’? Perhaps I just don’t understand the “science”. Or perhaps “science” as we’re being taught to believe it, is full of holes and hidden motives.

Or perhaps, what started out as a benevolent effort to help humankind, became corrupted and twisted into a sinister agenda to perform horrific experimentation on the whole population.

I can’t give you the definitive answer to that. I don’t believe that all scientists are corrupt and have hidden agendas. But I do believe that some do. And I do believe that those “world leaders” and scientists bent on transhumanism/genetic modifications/immortality (for their own people)/depopulation-slavery(for everyone else), has hijacked the scientific/medical/health communities, and are initiating their own forms of control and influence to initiate their “great reset”, which is another way of saying “reset the human race”.

So I shouldn’t have been shocked and surprised to learn that studies of “live parasites” in vaccines is a real thing. I’m not saying they’re used in ALL vaccines, but they are certainly being used in some.

“In a one-two punch, a malaria vaccine in development pairs a shot of the live parasite that causes the disease with a whammy of infection-fighting drugs to immediately quell it.”A malaria vaccine with live parasites shows promise in a small trial

Sure, Jan.

From the same article:

“Adrian Hill, a vaccinologist at the University of Oxford and director of the Jenner Institute who is involved with the R21 malaria vaccine: “If you give people [in Africa] a whopping dose of malaria and then for any reason that drug is expired or it isn’t the right drug or they took it too late — who’s going to take responsibility for that?”A malaria vaccine with live parasites shows promise in a small trial

Another article, unironically on the same date (June 30, 2021) as the previous one, states the following:

“Participants in the study, published on 30 June in Nature1, were given a shot containing live Plasmodium falciparum parasites, along with drugs to kill any parasites that reached the liver or bloodstream, where they can cause malaria symptoms. Participants were then intentionally infected with malaria three months later to test the vaccine’s efficacy.”

“Several malaria vaccines are in development. The most advanced — RTS,S — has been given to more than 650,000 children as part of a pilot programme in three African countries to assess its safety and efficacy, as well as the logistics of rolling it out.

Another vaccine, called R21, was recently shown to be up to 77% effective in a trial of 450 young children, and a larger study is under way.

Both of these use the same malaria protein, called circumsporozoite protein, to trigger immune responses. That protein decorates the outside of the sporozoite form of the parasite, the stage in its life cycle when it first enters the human body from the salivary glands of infected mosquitoes.

Vaccine made of live malaria parasites shows early success

So let me get this straight… They are trying to combat malaria, by pumping you full of live parasites that causes malaria, in order to cure/immunize against… malaria…?

Does this make sense to anyone? Wouldn’t it be more prudent to use, say, a highly efficacious anti-parasitic drug – like, oh… I don’t know… Ivermectin, perhaps, if/when a parasitic infestation occurs?

[ https://pubmed.ncbi.nlm.nih.gov/31948767/ ] “Ivermectin as a novel complementary malaria control tool to reduce incidence and prevalence: a modelling study”

Why deliberately inundate someone with parasites just to “possibly” immunize them from the very same thing? Then that leaves the very real dilemma… what if the immunization doesn’t work, and you’re left with a body full of parasites? Does anyone really want to take this chance? I can understand testing the correct dosage of Ivermectin to combat the amount of parasitic infestation, but no – it’s “Jump right to vaccines! Even though we don’t know if this will work either, let’s just go ahead and infect hundreds of thousands of innocent lives with live parasites and/or parasite proteins! What could possibly go wrong?”

And how HORRIFIC to be testing vaccines on children! Regardless if the vaccine has a live parasite or if it’s a protein from the parasite that HELPS them get infected… it is still an outrageous proposal to deliberately inoculate them and TEST the vaccine on them! And then are we to conclude that they are going to be deliberately infected with malaria (more parasites) to test the vaccine efficacy in later weeks/months?

650,000 babies and children?! Are you kidding me? In what world is this okay? This is outrageous and should automatically be labeled a crime against humanity. Maybe they wouldn’t be infested with malaria if they weren’t INTENTIONALLY INJECTED WITH A MALARIA VACCINE to begin with. All in the supposed “proposed” hope of “curing” them from malaria? Am I the only one who finds this absolutely ridiculous and atrocious? How about we stop experimenting on human lives and parasites to begin with? Perhaps if mad scientists weren’t genetically modifying everything under the sun, we wouldn’t be having these issues.

[ https://pubmed.ncbi.nlm.nih.gov/29077880/ ] “Repetitive sequences in malaria parasite proteins”:

“Five species of parasite cause malaria in humans with the most severe disease caused by Plasmodium falciparum.

We discuss the diverse roles of low-complexity repetitive sequences throughout the parasite life cycle, from mediating protein-protein interactions to enabling the parasite to evade the host immune system.”

Now why would they want to enable the parasite to evade the host immune system…?

And going back to Ivermectin, touted a “wonder drug” (which is also used as a prophylactic treatment), is there something to be said for an anti-parasitic drug that not only works against parasites, but also works wonders on SEVERAL different ailments? Or… could it be possible that all ailments are caused by parasites?

Blood clots, heart attacks, strokes, encephalitis, lung disease, pneumonia, kidney issues, gout, lupus, etc., etc., etc., etc. A few examples that help lend credence to this theory are presented below (embellishments have been added for emphasis):

Arthritis:

[ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003687/ ] “Toxoplasmosis seroprevalence in rheumatoid arthritis patients: A systematic review and meta-analysis”:

“Toxoplasmosis is a cosmopolitan infection caused by an intracellular obligatory protozoan, Toxoplasma gondii. Infection to this parasite in immunocompetent patients is usually asymptomatic, but today it is believed that the infection can be a risk factor for a variety of diseases, including rheumatoid arthritis (RA). RA is an autoimmune disease and the most common type of inflammatory arthritis that is a major cause of disability.”

Blood Clots:

[ https://www.news-medical.net/news/20200413/Study-looks-into-how-malaria-parasite-evades-the-immune-system.aspx ] “Study looks into how malaria parasite evades the immune system”:

The parasite causing the most severe form of human malaria uses proteins to make red blood cells sticky, making it harder for the immune system to destroy it and leading to potentially fatal blood clots. New research at the Crick has identified how the parasite may control this process.”

Central Nervous System Disorders:

[ https://www.verywellhealth.com/parasitic-infections-of-the-central-nervous-system-2488670 ] “Parasitic Infections of the Central Nervous System”:

“Trypanosomiasis, also called sleeping sickness, is caused by the protozoan parasites Trypanosoma brucei gambiense or Trypanosoma brucei rhodesiense. Like malaria, the parasite is spread by an insect host.

 

After a period of time, sometimes years, the parasite spreads from the blood to the brain, leading to meningoencephalitis and swelling. A headache, difficulty thinking, personality changes, and movement disorders such as tremor or ataxia (lack of coordination) can result.

Heart Attack / Myocardium / Pericardium:

[ https://heart.bmj.com/content/103/9/651 ] “Cardiac manifestations of parasitic diseases”:

The heart may be affected directly or indirectly by a variety of protozoa and helminths. This involvement may manifest in different ways, but the syndromes resulting from impairment of the myocardium and pericardium are the most frequent. The myocardium may be invaded by parasites that trigger local inflammatory response with subsequent myocarditis or cardiomyopathy

Pneumonia

[ https://thorax.bmj.com/content/66/6/528 ] “Parasitic infections of the lung: a guide for the respiratory physician”:

“Parasitic infections of the lung occur worldwide among both immunocompetent and immunocompromised patients and may affect the respiratory system in a variety of ways. This review provides an update on the presenting symptoms, signs, investigation and management of diseases affecting the lung caused by protozoa, nematodes and trematodes. The clinical presentations and radiographic findings of several of these diseases may mimic tuberculosis and malignancy. It is important to consider parasitic infections in the differential diagnosis of such lung diseases. If identified early, most parasitic diseases that affect the lung are curable with medical or surgical treatments.”

Seizures & Strokes (Gastrointestinal Complications)

[ https://www.verywellhealth.com/parasitic-infections-of-the-central-nervous-system-2488670 ] “Parasitic Infections of the Central Nervous System”:

“Paragonimiasis is a parasitic infection with a flatworm which may enter the body through eating undercooked crab or crayfish. It is rare in the United States, though several cases have been reported in the Midwest. Most commonly it is found in East Asian countries.

The parasite does not often affect the central nervous system but the parasite may reach the brain either through the bloodstream or through the foramina at the base of the skull. The adult form of the parasite both releases inflammatory substances and tunnels through tissues, which can result in headaches, seizures, and strokes.”

[ https://www.verywellhealth.com/symptoms-and-complications-of-chagas-disease-4163007 ] “Symptoms of Chagas Disease”:

“The symptoms of Chagas disease, an infection caused by a protozoan parasite called Trypanosoma cruzi (T. cruzi), resemble those of the flu—at least at first. When the acute phase of the disease resolves, however, the T. cruzi parasite can persist in the body for many years, even in people who appear entirely healthy. Many years later, often after decades, a chronic form of Chagas disease can develop, producing cardiac problems, gastrointestinal problems, or both.”

The Rod of Asclepius

“The probable medical origin of this ancient Greek symbol with a snake wrapped around a staff is the ‘worm theory’ that dates back to about 1500 BC. It was a description of treatment for the parasitic Guinea worm written on papyrus, said to be among the first ancient Egyptian medical documents. Ancient physicians probably used signs with a worm on a stick to advertising the worm treatment service they offered.”The Rod of Asclepius Symbol – History And Meaning

Perhaps the reason that Ivermectin is such a potent medicine against multiple illnesses and viruses, is because every ailment is caused by one parasite or another (or a combination of them).

If that is true, it makes one wonder why Ivermectin is so highly condemned in the medical/science community. Not all of the medical/science community, of course. It only seems to be the organizations who are incredibly politically and financially charged to do so. Who also just happen to work in conjunction with the huge alphabet government agencies, as well as the big tech / big pharma, and the mainstream media.

Hm… nothing suspicious there, right? And it’s not enough that the places who suffer the most from these diseases are also the ones selected for “investigational/experimental” trials of the very vaccines supposedly touted to immunize against the disease.

Now one could say, “Well, that’s the whole point. The whole country is suffering from this awful disease. So of course they’d want to cure them from it. So they’ll be the ones getting the injections. Duh!”

However, if you really dig into the history and the motives of those doing the “curing”, you will come to realize that they have no altruistic reason for doing so (despite what they say) and instead these “philanthropists” end up making BILLIONS of dollars for doing so. To add onto that, the REAL stories of painful and horrific side effects and deaths caused by these vaccines go mainly unheard of – kind of like how those who have taken the COVID vaccine and have suffered adverse side events are being censored and banned and IGNORED in the mainstream media and in hospitals worldwide. Their accounts also largely being wiped out from big tech platforms.

Now doesn’t it make you wonder, if they can wipe out all of these accounts and silence this awful widespread detrimental effects of the COVID vaccines, can you imagine how many MORE victims of vaccines that were touted as “miraculous cures” (just like the COVID vaccine…) that were inoculated in other countries, never got a chance to tell their stories? Since most of them were from poorly developed countries, and have a different language from the English speaking community, and don’t have common access to the internet… The only story we hear are the ones doing the vaccinating. And of course, according to them, it’s going “fabulously”.

So do you really believe that a known eugenicist, whose father worked with developing Planned Parenthood – the founder who was Margaret Sanger, who outrightly declared her desire to “wipe out the unfit” – that ranged from anyone who was poor, useless eater, African-American, mentally ill, disabled… do you really believe that this BILLIONAIRE, whose history is also connected with Jeffrey Epstein – a convicted child predator/child-trafficker – actually CARES about the human race so much to cure them all with a vaccine?

Bill Gates / United Nations

I smell a

Or, in the case of this post, a parasite.

And again you have to wonder, if Ivermectin is highly effective against parasites and cures many ailments… and the COVID vaccines (and other vaccines) have live parasites in them… then what is the real reason for the high suppression and smear campaign against using Ivermectin? So much so, that it has been banned in many places and some doctors ARRESTED and/or threatened with legal action and a revoke on their license for prescribing it to their patients, although it has been on the market FOR YEARS and approved as a safe medicine?…

Well, I leave that for you to contemplate.

For additional reading:

[ https://pubmed.ncbi.nlm.nih.gov/16778323/ ] “Genetically modified live attenuated parasites as vaccines for leishmaniasis”
[ https://pubmed.ncbi.nlm.nih.gov/30295650/ ] “CRISPR/Cas9 Gene Editing to Make Conditional Mutants of Human Malaria Parasite P. falciparum”
[ https://newatlas.com/science/crispr-gene-edited-parasite-leishmaniasis-vaccine/ ] “CRISPR-gene-edited parasite leads to unique new vaccine”
[ https://www.bu.edu/articles/2021/malaria-vaccine-approved-by-world-health-organization/ ] “Malaria Vaccine—the First Ever to Immunize against a Parasitic Infection—Gets Green Light from WHO”

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 Jeremytitus from Pixabay (with slight alteration)

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Jerm Warfare Interview with Dr. Zelenko: “These “vaccines”, which I call ‘poison death shots’ “

“The only reason you’d vaccinate your child is if you believe in child sacrifice.”

Dr. Zelenko, the doctor who created a treatment protocol for COVID, sits down with Jerm Warfare to discuss COVID, the dangers of the vaccines, and the worldwide suppression and agendas that are occurring around us.

The below video of the interview has been transcribed in full, with some embellishment added for emphasis.

Intro message from Dr. Zelenko: “Hi, my name is Dr. Vladimir Zelenko, I’m the original owner of the Zelenko protocol, which is a pre-hospital treatment for COVID-19.

What I believe is going on: that the enemies of humanity have weaponized fear and anxiety in order to effectuate a change in your life to mold society into the direction that they believe to be correct. And that involves taking away our freedom, and anxiety is a tool to which they enslave us.

So I’m here just to give you a simple message: that COVID-19 is highly treatable. There are treatment approaches as well as prevention – preventive, prophylactic approaches, and there’s no need to be afraid. There’s plenty of information available and even over the counter options without prescriptions that can save your life. You really don’t have any reason to be afraid once you have the right information. The information will set your mind and your soul free. And you don’t have to live with paralyzing anxiety.”

Jerm Warfare @1:54: “My name is Jerm. This is Jerm Warfare, the battle of ideas. That was the face and the voice of Dr. Vladimir Zelenko who is joining me right now on the other side.

It’s a great pleasure, Dr. Zelenko. Thank you for being here.”

Dr. Vladimir Zelenko: “Thank you so much for having me.”

Jerm Warfare: “You posted a video saying that your cancer has returned.”

” – worst global crime in the history of humanity.”

Dr. Vladimir Zelenko @2:18: “Yeah, I have a very rare – actually the rarest form of cancer there is. And there’s around 10 cases a year in the world. Always found at autopsy. And I was diagnosed with it three and half years ago during an emergency surgery, where they thought that I had a blood clot and turned out to be a tumor that killed my right lung in the pulmonary artery. I had that resected and I went through very difficult chemo which I had to design myself, cause there was no treatment available.

And that was good for two years, and then it came back last summer. Had another open heart surgery and had my heart valves replaced because of the tumor. And then just last week I found out it came back again, again in the pulmonary artery. And so now we’re putting together a plan to deal with this, but the game is not over. I’m very hopeful and optimistic about the future. Both mine and that of the world.

I really believe that my heart is still beating because of the prayers and the positive energy of so many decent people around the world. It’s what happened last time. I had millions of people praying. And so statistically, naturally I shouldn’t really be talking to you. I should be under the ground. And yet God has spared me for now, and I ended up, just a few years after having this type of cancer diagnosed, being the tip of the spear of the worst global crime in the history of humanity. And so part of the reason I was spared is becoming… revealed to me, I would say. But God’s ways are very mysterious, so.”

Jerm Warfare: “If you get through, which I’m hoping you will, you can call it the Zelenko Miracle.”

Dr. Vladimir Zelenko: “Well, listen, it’s already a miracle, every second of my life. And your life is a miracle. And those are things that we don’t necessarily focus on or appreciate, until our lives are threatened.

See the address between life and death is something very familiar to me. And so when someone lives in that state of being, you realize that: I want to say Happy Birthday to you. And not because – I don’t really think it’s your biological birthday, but what it is, is that every second of existence is a recreation; creation ex nihilo, something from nothing. God is making us in the present tense. And so since we’re being made every nano-second, that implies a few things. That He knows about us, He cares about us, He wants us to be. And if He wants us to be then you’re never alone. If you’re never alone there’s no room for anxiety.”

Government’s protocol: ‘Send them home and give them tylenol’
Meanwhile, patients were getting sicker and eventually put on ventilators – in which 80% DIED.

Jerm Warfare @5:08: “This – let’s go back 18 months or so. Life was somewhat normal, and then suddenly this weird thing happened.”

Dr. Vladimir Zelenko: “So I didn’t choose COVID, it chose me. What I mean by that is that I was practicing family medicine in upstate New York, in a small community of 35,000 people that live within a square mile. Very high population density. And when COVID arrived, it spread to everyone. Immediately. And I found my practice, my little practice of – we used to see 50 patients a day – inundated with over 250 patients. And there was no treatment at that time.

The government was telling us, “Send people home. Give them tylenol. When they get sicker, send them to the hospital. They’ll end up on a respirator.” And 80% were dying… on the ventilator. So that didn’t seem like a good idea to me. So, just like 3 years before, I had to develop my own cancer treatment, because nothing existed. I figured, well, why not innovate and find something to help my patients. These are people that I care about; these are people that I’ve cared about for 2 decades.

And so, I actually prayed; at 2 o’clock in the morning. I couldn’t sleep – You know, when people look at you and say, “Doctor, please help us.” And they – and you care about them, and then you have nothing to offer them. It’s a terrible feeling.

It’s, it’s – so, I just was studying what other countries have been doing. And something made sense to me. That in South Korea they were using hydroxychloroquine and zinc. And France, in Marseille, France, they were using hydroxychloroquine, azithromycin. And I understood the mechanism of action of these drugs and I said, you know, why don’t we just combine the three of them, modify the dosing and see what happens? Why not? This is battlefield medicine. You know? This is World War 3, the whole world is fighting the same virus, there’s no studies, there’s nothing that I could rely upon. So what do you do? You innovate.

They say necessity is the mother of all innovation. I had a necessity. I had to take care of my patients. I’m an outpatient doctor. Meaning pre-hospital doctor. My job is to keep people out of the hospital. That’s what I’ve always done, 20 years, in every other aspect of medicine. So why would I allow my patients to go home and just get sicker? It didn’t make sense.”

Dr. Zelenko develops a treatment protocol for COVID

@7:38: “So, since I understood the virology, I understood that this virus is an RNA virus that uses certain pathway for viral replication, and I found out that zinc inhibits that process, so zinc was the bullet. And I said, okay. But there was a problem with zinc. It didn’t get into the cell. Due to biochemical reasons. And so it was having like a bullet without a gun. So I needed a gun.

And it turned out that hydroxychloroquine is a zinc delivery system. So zinc ionophore; it lets zinc go from outside the cell to inside the cell. And by doing that we were able to inhibit the RNA dependent RNA polymerase; it’s just an enzyme, but all the COVID strains were using to… to use to make copies of themselves. And I shut down viral replication. So in other words, zinc was able to get to the right place at the right time, and stop the virus from making copies of itself. So that was the mechanism of action.

It was theoretical, but I deployed it. I also didn’t treat everyone. I treated the high-risk patients. And the way I found out who was high-risk, I just called the ICU near me, and I asked the doctor there, who is dying? And they said to me, “well, the old people and the people with chronic illnesses.” I said, “How about the younger people?” They said, “We’re not seeing them in ICU.” So right away I knew that this virus doesn’t kill equally.

So, I didn’t have any resources. Half my staff was sick, the outpatient service was like ‘blood-draw’, and radiology were closed. The hospitals were at near capacity. So I was like walking through my office; it was like a bomb went off. A mass casualty event – people all over. And so I had to triage. I had to make decisions; who to, who would get my attention. And who was low-risk enough that I can send them home. So I basically sent home everyone who wasn’t dying and it was young. And left the older patients; all those that had chronic medical problems.”

Treatment needs to be started IMMEDIATELY – against government “recommendations”

@9:46: “And I started treating them immediately. I didn’t wait for the results of tests. The tests took a week to get back. If I would wait a week, by the time the test result came back, the patient was dead. So instead of – I did the test, but I wouldn’t wait to treat – I used my head and said, “well, you know, the whole community has COVID, there’s no flu, they have all the symptoms, they’ve been exposed, this person has COVID.” Until proven otherwise. And I would treat them immediately. Within the first few days of the onset of symptoms.

From the moment I did that, people stopped going to the hospital and dying. So initially I didn’t believe it. I thought it was a fluke or – I couldn’t believe – But after 50 patients or so, I realized that I… stumbled across, or God gave a gift, of something that is a potential answer to a global problem that has no treatment.”

“Look, COVID is two diseases. There’s the viral infection phase, which is… lasts around 5 days/6 days. And then the immune reaction, your body’s immune system goes on overdrive and it’s the body’s immune reaction that kills the person. It destroys the lungs and causes blood clots. But the immune reaction does not start until a week – 6-7 days into the illness. So the key is to destroy the virus before then, so that the immune reaction, so the monster doesn’t wake up. We have a latent monster inside us – the immune system, in this particular case, and it’s ready to destroy the person. And it takes around a week to wake up. So if we could treat this infection within the first few days, it never wakes up. No problem. Patients get better.”

Media and NIH against the use of hydroxychloroquine – not interested in the treatment of COVID

Jerm Warfare @11:35: “Now, the elephant in the room is the amount of negative press, as you are well aware, surrounding hydroxychloroquine. I mean, Donald Trump, he spoke very highly of it. And funnily enough he took your treatment, didn’t he? As well as a bunch of people in the White House.”

Dr. Vladimir Zelenko: “Yeah, I ended up treating most of them. What happened was that I made a video addressed to the president, telling – I felt like a front line soldier that found an important enemy map. I needed to get it to the five-star general immediately. Didn’t have time to go through the chain of command.

So I made a video and it was addressed to the president, and the next day his chief of staff, Mark Meadows, calls me on my cell phone. I’m not making – I wouldn’t believe it unless it happened to me. But that’s what happened. And then I told him what I was doing; they were interested. Two days later the commissioner of the FDA is calling me on my cell phone, in Wuhan.

@12:32: And then the – because no one knew what to do. Don’t you understand that at that time, I wasn’t saying that my treatment is the best treatment. I was saying it’s the only treatment! So, so people were looking for solutions. And so then he referred me to the NIH, which was a deadend. They weren’t interested.

And then Rudy Giuliani called me. And I ended up doing a podcast with Rudy; became my good friend. And millions of people saw it. And from that podcast my life has never been the same again. Um, so that’s how people got to know me. And I’ve ended up advising governments and hospital systems and thousands of other physicians.

Um, so I also sent a letter to the president after a few hundred patients summarizing my experience and making my recommendations. And I didn’t know if the president got it or not. Until there was a news conference where President Trump announces to the world that he’s taking hydroxychloroquine. And he says, “Yeah, I got a letter from a, your upstate New York doctor.” And he was telling me this and this and this. I couldn’t believe it. – [Jerm Warfare: “How did you feel?”] – it’s the president of the United States. So, that was pretty cool. And so, that’s how I got involved.

“COVID-19 is an artificially made bioweapon”

@13:50: But, to understand the essence of the problem, we need to understand the essence of the problem. And everything else will make sense. So if I would’ve told you 18 months ago that COVID-19 is an artificially made bioweapon, I would immediately be labeled a conspiracy theorist. [Jerm Warfare: “Yes.”] Now, even the liberal media admits that this is an artificially made bioweapon. It’s a conspiracy, it’s just not a theory. It’s a conspiracy to commit mass murder and genocide.

And to tell you to what degree of resolution we know things – so for example, I can tell you like this, in 1999, that the Ralph Baric, Baric, in the University of North Carolina, at Chapel Hill, modified a surface protein on a bat coronavirus, and made it be able to infect human beings. And he has a patent number associated with that modification.

And then it became, this type of research became illegal in America. It was outsourced by Fauci and the NIH, to Wuhan! And then in 2005 or so, they were able to augment the lethality of this virus, so that it, it can destroy human lungs and cause blood clots. And we know the patent number is associated with those changes.

So no one’s denying that this is an artificially made bioweapon. So, okay. So now you have to understand why is there such opposition to the treatment of it in the pre-hospital setting. Cause what is the real desire goal of this bioweapon. It’s not to kill everyone. It’s to scare everyone. And if you studied psychological warfare, which I have, if you use fear – prolonged fear – and isolation: lockdown, what you do is you psychologically destroy the person. Most people will be compensated.

And then you dangle a false promise: the vaccine, and because you’re living in such chronic pain, and fear, you will gravitate – not intellectually – towards something that, anything, that will alleviate that emotional pain that you’re in. Now, that explains why people get so belligerent if you challenge them. Because if you challenge someone’s narrative, that they bought into, what you’re really doing is bringing them back into that anxiety state, and they, it causes so much pain they can’t stand it. So you can’t reason with them. It’s not a – it’s a super rational transformation of – it’s a way of enslaving people.

Denying the use of hydroxychloroquine and ivermectin – because THEY WORK

@16:31: Now, the problem with hydroxychloroquine and ivermectin, for example, is that they work! And since they work, what that means is that it could reduce the amount of anxiety and fear in the world, which is contrary to the whole point of the bioweapon. It’s a weapon against the bioweapon.

So, you have to ask yourself, why was this released? Why was this bioweapon made? Why is there such a effort – sorry – why is there such a global coordinated attempt to maintain global fear? And there’s an answer.

Um, in 2015 – by the way, I have a disclaimer. I want no one to believe me. Please do not believe anything that I’m saying. But, you can take that information that I am giving you, and I’m giving you very specific information, and go do your due diligence. Do your research. Don’t make the same mistake that you did with the governments, with me. Don’t buy into my narrative. But at least listen. And then, go and look into it, do your research, your due diligence, your – use your brain. And then come to a conclusion. And whatever that conclusion is, it’s yours. But the point is, hear the other side.

Bill Gates and the eugenics agenda

@17:51: So anyway, so with that disclaimer, I’m going to say that in 2015, you can google, ‘Bill Gates, Ted lecture’. So this sociopath – [Jerm Warfare: “I saw it. I saw it.”] So this sociopath calls for the reduction of the world population, because of global warming. Okay. So first of all, what kind of human being, uh, feels entitled to decide how many people should live on the planet or not? So that’s someone who doesn’t believe in the divine nature of humanity. That’s someone believes that in eugenics, or survival of the fittest, or the godless version of our lives.

But anyway, I have a good joke for you, by the way.

A child goes to his mother and says, “Where did we come from?” So the mother says, “Well, we’re made in the image of God.” And then the child goes to the father and says, “Where did we come from?” And the father says, “We evolved from monkeys.” So the child’s confused. So he goes back to the mother and looks for an explanation. So the mother says, “That’s not a contradiction. That’s my side of the family, and that’s his side of the family.” [Jerm Warfare laughs]

So Bill Gates belongs on that, group of people, belong to the monkey side of humanity. Whereas most humanity belongs to the – the wind made in the image of God department. Now, since they think they’re the biggest monkey, they think they’re on top of the food chain. That they can do whatever they want with us.

So here – I’m going to ask you a question. The same sociopath – I’m picking on him, but he’s just representative of a mentality – in last year said that 7 billion people need to vaccinated. So one simple question. Why would I take a vaccine, supported and funded by someone – for my health, a vaccine for my health – supported by someone who wants to reduce the world population? [Jerm Warfare: “It makes no sense.”]

Risk versus benefit analysis: medical necessity / efficacy / safety

@19:57: Okay, so, if I evaluate any treatment, any vaccine, anything I do to someone, I do a risk versus benefit analysis. If what I’m going to do may be risky, but does the benefit outweigh the risk? Otherwise, why would I do it? So, to understand if something is beneficial, you need to assess three things.

Whether you need it: medical necessity. You know a surgeon who operates on everyone is not a surgeon. He’s a butcher. He’s not using medical judgement. Just because someone came to your office doesn’t mean you have to cut him. There has to be a need for it, a reason for it. And the real surgeons know when not to cut. A real doctor knows when not to do something. So necessity.

Does it work? Efficacy. That’ll be useful, right? If I’m going to do something to someone, it better work.

And is it safe?

Though, if you analyze these vaccines from that perspective, and I can do that for you, I don’t know how much time we have, but – [Jerm Warfare: “No, please. I’ve got all the time.”] All right, so let’s look at medical necessity.

Without a vaccine: healthy children have a 99.998% survival rate /
“For every one child that dies from COVID-19 naturally, a hundred will die from the vaccine.”

@21:05: 18 and under, healthy children, have a 99.998% survival rate, according to the CDC, with no treatment from COVID. Why would I immunize a group, a demographic, that has a near 100% chance of recovery with NO treatment, with an experimental substance of questionable efficacy and known danger? The answer is I wouldn’t. Unless, I believe in child sacrifice. Doctor, Dr. Michael – “

Jerm Warfare: “Yeah. Exactly right. But – sorry, sorry, sorry – doctor, the media keeps pushing out a different story. So the questions is, who do you believe?”

Dr. Vladimir Zelenko: “Well, you can look at the CDC and see the survival rate of COVID-19. Um, as a matter of fact, I mean I can look at the day outside right now and say it’s night. That doesn’t mean it’s true. So the media is a tool of the fear. Maintaining the fear. So, getting back to my point, which was that – yeah, the young demographic has a 100% survival, essentially, so why would I do something that would threaten that demographic?

If you look at Dr. Michael Yeadon, who was the head of Pfizer, vice president of Pfizer[Jerm Warfare: “Yeah, he was on my podcast also.”] So, you know what he says? The guy is a world expert on vaccine development. And he did his statistical analysis, and he said the following, and he said this to me directly, because I’m friends with him and I called him up, and he said “For every one child that dies from COVID-19 naturally, a hundred will die from the vaccine.” 

Jerm Warfare: “That is not something I want to hear, doc.”

Dr. Vladimir Zelenko: “Well it’s not about what you want to hear or don’t want to hear, it’s about the truth. I don’t want to hear it either but it’s not going to help the children that are going to be sacrificed. 

Let me ask you a question. What’s the difference if I take a child, let’s say a five year old, and cut its throat, or throw this child off a cliff, or into a volcano or whatever, or inject them with something that they don’t need because they’re going to get better anyway, and it has a 100 to 1 kill ratio? [Jerm Warfare: “Yeah, no… this, um – “]

Without a vaccine: healthy 18-45 year olds have a 99.95% survival rate /
WITH TREATMENT (not vaccine), it’s near 100% survival rate

@23:26: So, okay, I’m gonna finish. Now, if we look at 18 to 45, many healthy adults, so the survival benefit there is according to the CDC, is 99.95%. With treatment, it’s near a 100%. So the same question. Why would I vaccinate a demographic of healthy adults, with something that, against the virus, that they’re gonna get better from, and with something that may kill them? It just doesn’t make sense.

And just yesterday, it was published, multiple studies, that proved what we all knew anyway, that natural immunity is multiple – many many times better than vaccine induced immunity. Which means, anyone who had COVID already and has antibodies have superior antibodies. So why would I inject in them a liquid that makes inferior antibodies and puts them at risk? There’s no medical – just – there’s no medical necessity there.

Okay. Now let’s get to the problematic group. The high risk group, 45 and over, or those that have medical problems, have a death rate, globally, of 7.5%. That’s unacceptable. That is… a huge number of dead people. However, if you treat them, properly, all the data, all the clinical trials or the peer reviewed studies, they’re dozens of them that have corroborated my initial observations. Which I had published in a peer-reviewed international journal, that if you treat people properly, you reduce the death rate and hospitalization rate by 85%.

So, just to explain what that actually means, at a 600,000 dead Americans, we could’ve prevented 510,000 from going to the hospital. So I can reduce that death rate from 7.5% to around 1%. So now comes a good question. If we have something that with treatment, has a 1% death rate, in a sub – in a small demographic of high risk patients, perhaps it’s better to vaccinate than let them get sick. We have to – we have – it’s a good idea – thought. It’s a question. I’m not denying it.
 

By the way, if there were good, effective and safe COVID-19 vaccines, I would recommend them. I’m not against the vaccines, I’m against being stupid. And, so let’s look if these vaccines have – if they work!

Booster shots suggested even though the initial vaccines
DON’T WORK

@26:07: The three most vaccinated countries in the world: Israel, Gibraltar, and in the Indian Ocean there’s an island nation called Seychelles, they all have more than 80% vaccination rates. All the countries are experiencing massive outbreaks of delta variant.

The CDC director, I think her name – Walensky or whatever he name is, said two days ago that it seems according to the Israeli data, anyone who was vaccinated early, has a higher risk to end up in the hospital, in the ICU, and therefore you should take another shot. [Jerm Warfare: “Why?”]

I’ll tell you why in a minute. But, so, so it doesn’t work. Apparently.

And now let’s look at the safety concerns, which is really – could keep us busy for the next hour. Let’s divide safety concerns over time. Because they vary over time. So there’s the first time period would be, let’s say from the moment of injection to 3 months. It’ll be the acute period. Then there’s the subacute period from 3 months to 3 years. And then there’s the long-term, more than 3 years. And I want to break it up in this way because it’s important to understand the mechanisms of action.

The – I’m sorry, my kids are calling me. Um, from the moment of injection until 3 months, people are dying from blood clots. And we know exactly why. The Salk Institute from San Diego published a paper, a landmark paper a few months ago explaining the mechanism. From the moment you’re injected, your entire body becomes a spike factory. Producing a viral spike protein.”

Jerm Warfare: “Sorry, before you go on, can you just explain what that means? Cause we keep hearing about that.”

The “vaccine”/”poison death shots” cause dangerous spike proteins to produce in our body – leading to blood clots

Dr. Vladimir Zelenko @28:16: “Well, um, how do vaccines work? How – usually I would give you a piece of a virus, let’s say the flu virus. So, I’ll take a piece of it, not the whole living thing, although sometimes we do use living tenuated viruses, but in most cases – or polio – that’s a better example. I take a dead polio virus and I inject it into you. Your immune system recognizes that it doesn’t belong there. It mounts an immune response generating antibodies and now if you ever come into contact with real polio, all your soldiers are ready to pounce, and destroy it and you don’t get sick.

That’s how a normal, traditional vaccine would work. These quote/unquote vaccines, which I call ‘poison death shots’, they’re completely different. They don’t inject a piece of virus. At all. They inject a code, a formula, that converts your body into a factory that produces part of the virus. And a very specific part of the virus.

See the virus, coronavirus, is basically a ball with thorns. And it has these little spikes. Let’s call it the male organ. And in order to be able to get into the cell, it needs to attach to the receptor on the cell, which is the female organ. So the spike itself goes and finds its mate, and that allows the virus then to get into the cell. So, the spike is what actually gets the virus inside the cell.

So what we’re doing is giving you a code in the form of mRNA, which is the code. Your body’s cellular metabolism, your body’s own processes, are hijacked to manufacture all these little spikes. Not the whole virus, by the way. Just these little spikes. Trillions, hundreds of trillions of them, and it turns out that they migrate and end up in your blood vessels. Lining the endothelium, which is the inner skin. The inner lining of the blood vessel.

And it’s supposed to be smooth, obviously. Cause you have high rate of flow of blood cells, you don’t want them – [Jerm Warfare: “Yes, I understand.”] – you don’t want them to bump into stuff and break. In fact, all of a sudden you just coated lined wallpaper, inner lining of every vessel in your body with thorns. Little spikes. [Jerm Warfare: “Okay, yes.”] And then the blood cells get damaged. And when they get damaged, they leak stuff. That sets off a reaction in the body to cause blood clots.

So, the main cause of death in the first 3 months is blood clots in the form of heart attacks and strokes, or anywhere else. It could be kidneys, lungs, could be in your mesentery, your gut. So that’s what we’ve seen. And 40% of the deaths are happening within the first 3 days of injection.

How many people have to die from the COVID vaccines before we finally say, ENOUGH?

@31:45: Now, what’s the threshold of death? When do we say, you know, it’s too risky? It’s too much? In 1976 we had the swine flu vaccine. Um, it killed 26 people. The entire vaccine program was canceled.

According to the United States government already, this is according to the government, there’s 13,000 dead. According to the whistleblower, from the CDC, that wrote an affidavit, the number’s 45,000.

That’s not enough? I’m telling you, in 2009 there was a study on the system used for reporting. Called VAERS. That only 1% of events are actually reported. Now, I can make an argument, that maybe rashes are reported much less than death. Agreed. I’m not gonna deny that.

So what is the number? No one really took the time to figure it out. But, okay, it’s not 1%. So I’ll be very generous to VAERS. I’ll give ’em a 20% reporting rate. And that’s being generous. So what that means is that the number of deaths being reported, you have to multiply it by a factor of 5. [Jerm Warfare: “So over 200,000.] I think so.

And there are two other problems with this system. Which is that known reports are being scrubbed off the server. We have evidence of this. We have screenshots of reports that were there a few months ago that no longer exist. We can’t get ’em. And also I have colleagues that are trying to file reports. They lost patients, and the system won’t let them. It’s rejecting their reports, on technicalities.

So, there’s an obvious – and Senator Ron Johnson from Wisconsin is actually doing an investigation to see to what degree their suppression and obstruction and flow of true side effect information. So, that’s a lot of death already.

Issues of myocarditis and miscarriages – and no long-term assessment of the COVID vaccines

@33:55: The other problem is inflammation of the hearts. Called myocarditis. It damages the hearts it seems of young men. And the other problem is miscarriages in the first trimester in women that have been vaccinated is a much increased rate of losing their babies.

So that’s pretty bad. Remember, this is something that doesn’t work and you don’t need it. And then, let’s go to the longer term consequences. Well, it’s clear that the number of autoimmune diseases and cancers is going up. And there’s enough data concern/smoke, to require further inquiries to see if these mRNA vaccines are actually causing it. Remember, it went from laboratory to human use in less than a year. When on average it takes 10 years to vet a vaccine. So it’s not like we have long-term studies. So you need to know what’s going to be in a few years.

So there’s a concern already of autoimmune diseases and cancer – so that’s going to effect lifespan, and there’s also a real concern – there’s a leaked study from Pfizer that wasn’t supposed to get out. But someone leaked it from Japan. Where it showed the, when you inject it here [Dr. Zelenko points to his arm] where the vaccine actually ends up. And the largest amount ends up in the ovaries. So the question is, what is the long-term consequences on fertility? That has not been vet – that has not been ruled out. That has not been checked or assessed.

” – this vaccine program is the biggest threat to humanity in the history of humanity.”

@35:32: Okay. Now, but that’s – everything I just said is nothing compared to what I’m about to tell you. Between 3 months and 3 years, is a period where the world experts, the top minds in medicine and science, are SCREAMING, “Stop! You’re going to cause a genocide.”

So, for example. Remember, don’t believe me. Dr. Luc Montagnier, he happened to win the Nobel Prize – [Jerm Warfare: “For HIV.”] – for finding HIV. Yes. Pretty big boy. I wouldn’t say he’s the… he said like this. He’s never seen anything like this, and this vaccine program is the biggest threat to humanity in the history of humanity.

Okay. Then, Dr. Dolores Cahill, a top […] from Ireland, came out saying that within 2 years, she believes 90% of the people who got vaccinated will be dead.

Now, – [Jerm Warfare: “Wait! Two years?] – Yeah. So maybe she’s wrong. Maybe it’s 3 years. Or 4 years. And maybe it’s not 90%, what if it’s 5%? Not enough? So she’s raising a concern – hold on, and then Dr. Robert Malone invented the mRNA vaccine technology. It’s telling people, “Don’t take it. It’s too dangerous. The government is lying to you.”

And the, Dr. Michael Yeadon that I mentioned is saying the same exact thing.

Immune system, activated by the vaccine/virus, is attacking our own body –
Antibody Dependent Enhancement (ADE)

@37:15: What is the concern? And why are people going nuts about this? So, here’s the reason. In the 1960’s, an RSV vaccine was made, given to children, it killed children. No one understood why until they figured out that the children developed antibodies to RSV. And then when they were exposed to RSV, there was a – the immune system blew up and it was the immune system that killed the child. [Jerm Warfare: “What? The immune system?”]

It’s the child’s immune system that killed the child. It was an overreaction. That’s called antibody dependent enhancement. It’s not from the actual vaccine. What happens – listen again. They got the vaccine, they developed antibodies. Now you have these supposedly protective antibodies, then the RSV virus came, touched – came into contact with these antibodies and there was an explosion in unhealthy immune reaction.

Not every part of your immune system is good for you. You heard of autoimmune diseases? Lupus? Rheumatoid arthritis? That’s your body’s immune system attacking your body. That’s unhealthy. So it’s not always that your immune system is good for you.

So, in this particular case, the antibodies that were produced by the vaccine triggered a reaction, once coming into contact with the virus that killed the children.

So in 1970’s, there was something called the dengue fever virus vaccine, same thing happened. They would give it to people/adults; they died. It was the same exact mechanism of death called antibody dependent enhancement.

In all the attempts to make coronavirus vaccines, in the animal models, all of them manifested this reaction. And killed a large percentage of the animals that – in other words, the animals were vaccinated: mice, ferrets, and they produce antibodies, and then they’re purposefully infected with the virus that they’re immunized against. They’re challenged, to see if it works. And a large percentage of these animals died. Again, it’s called antibody dependent enhancement.

So here’s the question. Wouldn’t it be a good idea to rule that out by human beings, before you deploy a vaccine to 7 billion people?”

Jerm Warfare: “It sounds like an absolutely terrible idea. So, why – “

Leading experts warn of the many side effects of the vaccines –
and world suppression of the truth

Dr. Vladimir Zelenko @40:13: “That’s exactly what happened. Said – there’s 2 billion people already in the United States, there’s been a deployment of a substance that has the potential to kill the organism that it was given to. And that potential has not been excluded. And there’s a historical precedent for these things to happen. And it’s being done to people that don’t need the vaccine. And it doesn’t even work.

So, I’m going to make it very simple. Um, this vaccine is being deployed not for medical reasons. At all.

So I already told you, look, the causes, blood clots, inflammation of hearts, miscarriages, increased rates of cancer potentially, increased rates of autoimmune diseases, potential infertility, and the potential of this autoimmune death process, that it’s not me saying it! I am nobody. There are world experts in the fields; you mean, the guy who invented the vaccine – that’s not enough for you? Or the guy who ran Pfizer? Or the guy who won the Nobel Prize for finding HIV? That’s not enough?

These people – so what would be the normal rational thing to do? Would be, well, take a step back, let’s test these more to see if they’re safe. Forget about – you don’t need it, but still. So, do you see what’s going on here?

There is the suppression of life-saving medications, there’s the suppression of knowledge of life-saving treatments. Anyone who dares to say against the accepted narrative that the media is pumping, is deplatformed. It could be the world expert who made the mRNA vaccine who says something against the policy of the government is immediately deplatformed from every social media site. Why is that? And then, the actual side effects of these vaccines are being artificially suppressed, so that we don’t know the truth. And no one really needs this vaccine. Because I explained to you – though… what’s going on here?”

Jerm Warfare: “I mean, Dr. Lee Merritt has said very much the same thing.”

Dr. Vladimir Zelenko: “Yep, and Dr. Peter McCullough.

A need to reflect on our own values and freedom into the future

Jerm Warfare @42:47: “Yes. He also says the same thing. So, how – how do you, how do you respond, doc? What do you do, in a situation now when you’re hearing about the mandatory vaccines that are coming? And by the way, it’s not just in the United States. Our own government is now talking about making these vaccines mandatory.”

Dr. Vladimir Zelenko: “Define mandatory. In other words, they’re going to come down and hold you down, and put a needle in your arm?”

Jerm Warfare: “I don’t think that – to that degree, but I think you won’t be able to get employment, you won’t be able to go into shops, etc., etc.”

Dr. Vladimir Zelenko: “I wouldn’t worry about it; I’ll tell you why. Because there’ll be so many dead people, rotting corpses in the streets, that the worse it’ll get, it will look like a kindergarten, and you’ll have plenty of job openings.”

Jerm Warfare: [laughs] “I’ve never heard that. That is such a dark joke, but it’s so true.”

Dr. Vladimir Zelenko: “Look, I am not ready to sacrifice having a future for a few conveniences in the present. [Jerm Warfare: “Sure.”] I’d rather sacrifice the present, so that I have a future. And people have really messed up values. “All right. I can’t fly in a plane, so I’ll take the vaccine.” or, you know, “I’ll lose my job.” or, “I won’t be able to go to school.” And I look at these people and I say, well, you are making decisions on – that will potentially affect your lifespan and you’re doing it so willingly and blind – why? And so people are so gullible; it’s so easy to manipulate humanity.”

We’re in a life and death situation: not with the virus, but with the vaccine

Jerm Warfare @44:36: “Is it, is it literally a life and death kind of scenario? In your view.”

Dr. Vladimir Zelenko: “Absolutely, yes. We’re at World War 3. And you know, if the Germans were bombing over your head, you wouldn’t be asking that question. But the bombs that are being sent at us are invisible. And sugar-coated. And, I mean, there’s already hundreds of thousands of deaths from the vaccine. How much more death do you need to see before you say enough?”

Jerm Warfare: “Well they’ll say – they’ll respond and say yes, but it’s not because of the vaccine. It’s because of other things.”

Dr. Vladimir Zelenko: “Well they can say whatever they want. It’s just not consistent with truth. Not consistent with the data. And we know that COVID-19 is exceptionally treated.

It’s true that if there’s a fire and I don’t put it out, it’s going to burn the house down. So you’ve set a lot of fires, artificially. You go around and you set fires around the neighborhood and then you tell people, don’t put it out. Then the neighborhood burns down. Okay? That’s true. But doesn’t mean you have to put gasoline on the fire either. So, my answer to you is, don’t worry about the virus. Be prepared to deal with it. They’re over the counter options. And you’ll be fine. And don’t buy into the false – “

Assessing the difference between DNA and mRNA vaccines –
and the issues with “shedding”

Jerm Warfare @45:54: “Emma has got a question. She wants to know what your thoughts on the Johnson and Johnson vaccine. Because as far as I’m aware it’s not mRNA.”

Dr. Vladimir Zelenko: “Yeah, it’s worse. It’s a DNA vaccine. In other words, the way it works is, mRNA is limited to the cytoplasm of a cell. To the – let’s call it your living room. It gets into your living room and it uses your television and it makes copies using the equipment that’s in your living room. And those proteins that are made are what are potentially killing you.

The Johnson and Johnson is a DNA vaccine. And that gets into your bed where you are, lying there, in your pajamas, and goes right into your core, into your essence, and makes – messes with your DNA, and then becomes mRNA and – in other words, it’s deeper penetrating. It’s much worse. It’s like having someone – difference of this: someone in your living room and someone in your bed. Johnson and Johnson gets into – into you, real deep.

Now in Texas they have a flag, ‘don’t tread on me’. So I made a meme, ‘don’t shed on me.’ But uh, I don’t like shedding, but it’s not really a major problem for most people. Because what shedding is, is in the first 3 months after you get vaccinated, you’re actually shedding the spikes. And it comes through your breath, droplets, it comes through your skin, comes through other bodily fluids.

Now most people, it may mess up their periods, it may make you feel not so well, but it’s not an enough of a dose to cause real problems. Except in 2 categories of people. Someone who has a blood-clotting predisposition. There are conditions where people are more prone to blood clots. That could trigger blood clots. Because that’s what the main concern is, in the first few months.

And then, miscarriages. It seems to cause miscarriages in, you know, pregnant women. So, if – or women that want to get pregnant; it messes with their ability to get pregnant. So, but it’s a short-lived problem. So it’s not – it’s a problem, but it’s not a problem worth over emphasizing, because there’s much bigger problems.”

Jerm Warfare: “She says, yeah, especially around pregnant women.”

Dr. Vladimir Zelenko: “Yeah, so that – that’s a good question. Um, you don’t know who’s vaccinated, and again, if it’s more than 3 months they’re no longer radioactive. You know? But you don’t really know when and what – so, that becomes a hard question. So… pregnant women have to be a little bit more isolated, in my opinion, if they want to protect their pregnancies. But the majority of people should not isolate themselves because of shedding.

Inspiration and advice: ‘Stay away from bad, do good, and live’

@49:04: Whenever I need inspiration, I look back into bigger minds than me. And in the Psalms of David, King David writes the following, a very good prescription: ‘stay away from bad, do good, and live’. So that’s the prescription. So let’s break that up.

‘Stay away from bad’. Do not give into the fear, do not isolate yourself. Do not take a poison death shot. And if you did already, don’t do it again. Don’t harm yourself. Do no harm. Don’t destroy yourself psychologically, emotionally, and physically.

‘Do good’ means, that if you’re in the high risk category group, meaning anyone over the age of 45, or anyone with medical problems, or in my opinion anyone who got the vaccine, you should take prophylactics; it’s preventive therapy. And preventive therapy doesn’t mean to take another shot and make more bombs. Preventive therapy means that to prevent the detonation of those bombs that already exist by using antiviral drugs – um, and you can find them on my website: vladimirzelenkomd.com.

I have protocols with dosing and everything for prescription and for over the counter options. So people could have them in their hands. But they – and the idea is to protect yourself in advance so that you, if you do come into contact with the detonator, another virus, you don’t die. And if you do get sick, God forbid, you have to start treating day one. In other words, you don’t want the monster to wake up. And then you’ll live.”

Spirituality and the sanctity of life –
Godliness vs. godlessness

Jerm Warfare @51:03: “It seems like this is way more than a medical war that grew in. It seems like it’s a psychological war, isn’t it? Religious war, spiritual war, I don’t know what, but it’s certainly more – “

Dr. Vladimir Zelenko: “It’s a war against God. There are two systems of thought, that can’t co-exist anymore. There’s a system that is based on God centered consciousness. Which means like this, just follow the logic. If God makes you, that means your life, your life has sanctity. If your life has sanctity, that means you have human rights. If you have human rights, then it’s not in the realm of another human being to decide how long you should live and how many of us should be on the planet. That’s God’s department.

There’s another system, which is completely godless. It’s based on Darwin’s theories and Galton who developed eugenics. You know they were – he was a nephew of Charles Darwin. And their system is the survival of the fittest system. In other words, they believe that there’s a hierarchy of humanity, to be based on genetics or other factors, and it’s the strongest, on top of the food chain, that will dictate what happens to everyone else.

Now, this sounds like a fairy tale except that it killed 200,000,000 people 80 years ago. Because invariably it deteriorates into 3 categories of human beings. The super-human, the human and the sub-human. So the Nazis, the Aryans, believed that they were descendants of Aryan gods. And therefore felt entitled that they could enslave and murder anyone they wanted, and wage global war.

And the humans were the Anglo-Saxons, the Europeans that were meant to be enslaved and serve the super-humans. And the sub-humans that I belong to, the Jews, the slobs, the gypsies, handicapped, and political people that oppose them politically, they’re the sub-humans that needed to be thrown into gas chambers and then the ovens and vaporized into dust.

So, and this is not a fairytale. This is history. Recent history. So that mentality did not go away. That mentality went dormant for a bit, and now it’s woken up, but it’s not anti-semitic, actually. What it is, is something else.

On top of the super-human is these, what they perceive themselves as evolved higher level of consciousness people that think that they know better for what the rest of us need, and therefore can make policies that will control how many of us live, and how long we live. In reality, these are not evolved people. These are devolved pagans. These are sociopaths, these are wannabe deities, these are just the biblical historical replay of maniacs that are denying the existence of God and believe in their own immortality.

People who are dictating the rest of the world keep themselves hidden

@54:17: And what – so let’s – who are they? Um, honestly speaking, 70% of all corporate wealth in the world is owned by 150 people. So I would suspect it’s some – some people in that group. And because they control media, politics, academia, and one of their policies – what do they want?

The real people who are doing this are too smart to be in the news. It’s not Fauci, it’s not even Soros or Gates, or Schwab. Because the people that are really doing it are really really smart. And they hide themselves like layers of proxies, to do their bidding. And ‘why would I sacrifice myself – I’m too smart for that’.

But if you look at the World Economic Forum, which is a good example of despotic thinking – tyrannical thinking – and they crafted a 2030 UN plan. It’s already being implemented. And, you know, Hitler wrote Mein Kampf, and wrote it many years before he took control. He laid out his plans. These people are not even hiding their agenda. So what is their agenda? Go look at the 2030 World Economic Forum plan, and you’ll see – [Jerm Warfare: “You’ll own nothing.”] – and you’ll be happy, yeah.

What kind of sociopath, what kind of human being feels that they can decide whether you own property or not? Possessions or not? What else do they say? Um, you won’t eat meat except on special occasions. [Jerm Warfare: “And insects, also.”] All right. I didn’t hear that one. They – you won’t use fossil fuels. America will no longer be a super-power. A few European countries will run the world. There’ll be a billion refugees. So, what you have are – this guy, Schwab, said in 2016, it’s on an interview in French, that within 10 years, by 2026, everyone will have a digital tag and identifier in them.

Jerm Warfare: [jokes] “You are really ruining my Friday evening, doc.”

Test on humanity – on our decisions

Dr. Vladimir Zelenko @56:58: “You know, that’s good. Because reality – you need a reality check. And the next people that are willing to stand their ground and sacrifice even their own lives so that humanity’s – the soul of humanity is… remains. Because that’s, it’s an attack on the core of what is means to be a human being. And the core of our souls, and the core of our relationship with Creator.

And ultimately I think there’s a divine test, here. Which is, no one’s making you take this. You’re choosing to do it. There’s no such thing ‘you were forced’. Because, you could be pressured, you could be coerced, but you still have the ability to say ‘no’.

And if you put your trust – if I was God, I would be asking this following question: “I know you’re scared and the world is crazy. But who are you going to put your trust in? Me, who makes you? You’re going to ask me to fill the… your anxiety space? Are you going to ask me for protection? Because I’ll do it. Or are you going to go around to false gods, despotic governments, sociopathic oligarchs, and the golden calf of this vaccine? Because if you are going to do that, then let them protect you. Let’s see how that’s going to work out for you.”

Reflecting on the future – God conscious living vs. immorality

Jerm Warfare @58:20: “In front of you, doc, there is a crystal ball. What do you see?”

Dr. Vladimir Zelenko: “I see a glorious future. I see a… we’re in the cusp of a redemptive process. Where there’s going to be – people are going to self select into… God conscious living, versus idolatry.

And then I believe what the prophets say. Not me. That the spirit of inequity will be removed from the Earth. God will take out His big broom, clean out the garbage, and then the world will be filled with the knowledge and glory of God.

I think, I think that God has had enough of people who, for example, if these despots had their way, a 30 year old man who thinks he’s a woman would be sharing a bathroom with my 4 year old daughter. [Jerm Warfare: “It’s unreal.”]

So this type of erosion – you know, in the Bible it says that Sodom and Gomorrah were destroyed. The Talmud asks why. So one suggestion is because of immorality. The answer’s no. The whole world was immoral. What was so special about them that they were singled out? You know what the answer is? That they codified it into law. It became the law of the land. Immorality became codified as the norm.

[Jerm Warfare: “That’s what’s happening now.”] You think? What do you think I”m telling you this? So I think that we’re in a glorious journey that there’s going to be a transformation. It’s going to be bumpy. Be some turbulence. But at the end, the world will be cleaned up, just like the flood. And we’ll be left with, with people that want to live a God centered moral life.

I’m not afraid of dying. It’s not my department. You know? How I’m going to die, how long I’m going to live, no one knows. And it’s ultimately in God’s hands and He could do whatever He wants.

What I’m afraid of is living. In other words, am I living to my fullest potential? When I have to stand before the King of Kings, and give an accounting – he’s not going to ask me why I wasn’t like you. He’s going to ask me, “Why weren’t you like you could’ve been?” Me. Zev Zelenko. “Why didn’t you reach the potential that I had for you?”

And, so, I want to use my thoughts, of check and control, my speech, and my actions of check and control, and my time. I want to use that in a way that makes the world cleaner and better and healthier, and more Godly, and beautiful. I think that’s a worthy, worthy of my time and efforts. And that’s what I focus on, and that’s what I try to do. And that’s why I’m talking to you.

Jerm Warfare: “I’ve been waiting for 30 minutes to say what I’m about to say, but you are making medicine great again.

Thank you so much for your time. It’s been a great pleasure.”

Dr. Vladimir Zelenko: “God bless you. Thank you.” 

Jerm Warfare: “You too. Thank you, man.

My name is Jerm, this is Jerm Warfare, the battle of ideas.”

Thank you so much to Jerm Warfare and Dr. Vladimir Zelenko for this interview. Your efforts to spread awareness and the truth is extremely important especially in these suppressed times, where going against the narrative is ridiculed and censored.

And a special thank you to Dr. Zelenko and other doctors/healthcare providers who made the decision to help treat the people who needed it. Your compassion and integrity speaks volumes of your character and is the role model that people need to get through these uncertain times.

Lastly, a huge thank you to everyone for reading and spreading these messages. God bless.

Featured image by HeungSoon from Pixabay

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.

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