The Highwire with Del Bigtree - DEADLY MYOCARDITIS CLUSTERS IN INFANTS IS THE COVID VACCINE TO BLAME?

Episode Date: June 1, 2023

A recent unprecedented surge of deadly myocarditis in babies in England and Wales has been linked to enterovirus which is generally mild in infants. Del walks through mechanisms of the COVID-19 vaccines designed specifically to suppress toll-like receptors and why we should be looking into the possibility of this technology inadvertently turning once mild viruses into killers. #Enterovirus #mRNAVaccines #MyocarditisBecome a supporter of this podcast: https://www.spreaker.com/podcast/the-highwire-with-del-bigtree--3620606/support.

We really are trying to get you to understand how this scam happens. And so many of you are brand new to the high wire. We started this all the way back in the early, in early 2017, this show, where we were just this little nonprofit. We started in a closet with one camera in front of me and, you know, and a guy behind it that was editing. And, you know, Patrick and Catherine were there with me, just trying to make a show happen.

But what we were producing was the information we were winning in lawsuits through Aaron and Siri, winning against the CDC. went against the FDA and the LH. And it started creating this picture that we were able to understand of how the scam of vaccine safety is being done. And how there's a blindness to it. And by the way, they've never done a placebo study of any of the childhood vaccine. So I want to answer this question that you all keep writing in on that are joining us now. I know the COVID vaccine sucks.

But what about the rest of the childhood vaccine schedule? What about those vaccines? Well, they're exactly the same. COVID vaccine is just like every other vaccine. It was rushed on the market. In fact, it actually did have a placebo grip for a couple of weeks, which was better than any other study of any of the vaccines you've already given most of your children, unfortunately. But this is what I'm going to do is we're going to keep using COVID to help you understand how this scam works. This was triggered by a headline I saw this week. Take a look at this. Baby dies and nine more admitted to hospital

in unusual cluster of heart infections. WHO warns of a surreesome. in severe, there it is, myocarditis, a potentially deadly inflammation of the heart in South Wales and Southwest England. One baby dies. This is another headline about the same thing. One baby dies and eight others fight for life due to spike in unusually harmless virus. The sudden spike in the condition left health chiefs baffled. And an investigation has been launched to determine the causes of the spread. They're just mind-blown. We have no idea where this myocarditis, why all of a sudden is, you know, a regular virus that doesn't affect anybody now killing children and swelling their hearts. I know, don't get ahead of me. Don't get ahead of me

on this. We all heard myocarditis before. We know what causes myocarditis. But before we get into that, where you think you know this is going, let's just take a step back to pre-COVID. To a story we've shared with you of a lot on the high wire, because it's going to give you a lens into understanding what you're actually watching happen and will help you understand the childhood vaccine program. I want to talk about a guy named Dr. Peter Abe. Peter Abe is a world-renowned vaccinator. He is in charge of designing vaccine programs for the Middle East and underserved nations. He prides himself in the work that he's done. Well, Peter Abe decided, I don't know why, but since I think many of us that says, why don't you just do a vaccinated versus unvaccinated study?

Compare the health outcomes of those that are fully vaccinated to those that are completely unvaccinated and see who's actually healthier. If you've been watching the show, you know that Robert Kennedy and I sat before the National Institutes of Health. Tony Fauci sat right across from me. Francis Collins was across from Robert Kennedy. And we were asking simple questions like, why are you not doing any placebo studies? And why won't you compare the vaccinated to the unvaccinated? because if you did and you show that vaccinated are actually healthier than all the unvaccinated kids,

this conversation would be over. You know what they said to us? We will never do that study emphatically. I'm not going to get deep into that, but here is probably why. Dr. Peter Abe decides, you know what? I have a way to do that study. What he recognized is he had done a DTP vaccine program in the country of Guinea-Bissau Africa. And what he realized 30 years after this program was, you know what, because we were really specific on the

age groups of the children that were receiving this vaccine, and if you weren't in that age group, you didn't get it. And also because it was hard to get to certain villages, he realized retrospectively looking at it that we actually only vaccinated half the kids with this DTP vaccine, in some cases, a polio vaccine. And he realized it's totally randomized. By the nature of how we only got to half the kids, we have a perfectly randomized control trial across an entire country of, you know, similar human beings with similar diets and racial profiles. And so he said, I can do a perfect comparative study. And when he did that study, he was shocked at what he discovered.

Now, folks, the diphtheria-technist or pertussis vaccine is still used today. In fact, it is the most popular vaccine used in underserved nations. UNICEF and everybody are in on it. We have tried to sue. That's a whole other story. But here's why. When he looked at it, this is what he found. This is the paper on it.

The introduction of diphtheria pertustis and oral polio vaccines among young infants in an urban African community and natural experiment. What he found was DTP was associated with a five-fold higher mortality than being unvaccinated. What he found when he looked back was kids were dying at five times the rate if they got the vaccine. And that was if they got two vaccines at the same time. You look at this chart, diphtheria in oral polio, if you got both of those five times the rate. If you only got the DTP vaccine, those children died at 10 times the rate of those that didn't receive any vaccine at all. This blew his mind. Wait a minute.

And what he realized was they weren't dying of diphtheria, tetanus, and protesteris. The vaccine was protecting against the diseases it was aimed at, but it was clearly creating a susceptibility that was making them vulnerable and making other diseases more deadly, like, you know, dysentery. or malaria. They were dying at much higher rates than those that hadn't gotten this vaccine. But don't take my word for it. This is him explaining it to an audience. This is about vaccines. And I think it's important to recognize that no routine vaccine was tested for overall effect on mortality in randomized trials before being introduced. I guess most of you think that we know what our vaccines are doing, we don't. The program we are talking about at this time, the vaccine program,

was introduced sort of in the late 70s after the success with the eradication of smallpox. WSO made sort of the first immunization program for the low-income countries. While you comes out here, you had 2.3 times higher mortality if you were DTP vaccinated. And that is the most commonly used vaccine in the world. And note again that this is clearly worse for girls and for boys. It's not good for boys, but it's the girls do worse. When you introduce DTP booster, mortality goes up. When we introduce hepatitis B, which is also an inactivated vaccine, the same thing happened.

So by now we have shown negative effect for girls for six inactivated vaccines. DTP 1 is 20% higher mortality, but then when you come to DTP 3, it's 70% higher mortality for the girls for the boys. So the whooping cough vaccine or a pathosis vaccine was associated with two-fold higher mortality. And please note that the tendency is that this seems to be slightly worse for girls. You can have a vaccine which is fully protected against a specific disease, but associated with higher mortality. How is that possible? This is the first time, as he said, the study had ever been done. This is the truth, folks.

There has never, ever been a study looking at the vaccine program in America or England or anywhere looking at Did it actually increase the lifespan when he finally asked that very important question? Not the question. The only one they ever asked, as he said, is did it stop the virus or the bacteria that we were trying to protect you from? Yes, it did. But in the end, it killed more children. And that question has never been asked. Is our vaccine program killing more children?

We know, as we pointed out with Dr. Pierre-Corri, that we've gotten much more sick. We used to have a chronic illness rate of about 12 percent when we had 10 vaccines. And now it's 54% of autoimmune disease and neurological disorders in our children now that we have 52 vaccines or, you know, in 72 doses. And it keeps on climbing. So all of this to say what he's pointing out, and I want you to be clear about this, the vaccine blocked against, you know, disease, you know, at least the illness, the, it may not have stopped the infection, but it stopped them from being sick from it. but it caused a sort of a suppression of immune system that led to more death. This is Christina Stable Ben. This is someone that actually works with Peter Abe.

Now, just in case you think he's lost his mind as an anomaly, she did a TED talk on this. This is what she, how she described it. I'm a medical doctor and a researcher, and for the past 25 years, I've been working in the small West African country in Nair, Bissau. We started doing what nobody else had done before us. We evaluated the effect of vaccines on overall. all health. Before we started looking closer at DTP vaccine, it had only been studied for its protective

effects. In one study, we went back to historical data from when DTP vaccine was introduced in Ginebissau in the 1980s, and the results were scary. In spite of being protected against three deadly diseases, the introduction of DTP was associated with increased overall mortality. Children who received DTP vaccine had five times higher risk of dying than those who didn't. And this is just one example of many studies now done of DTP vaccine, and they all show the same. The protection against the three deadly diseases comes at a very high price, namely increased risk of dying.

So with the best of intentions, the use of DTP vaccine may kill more children than it saves. Based on these observations, that if we modify the existing vaccination schedule in low-income countries, then we could save 1.1 million. children every year. 1.1 million children, that's equivalent to more than 3,000 children every day with minor modifications of the vaccination program. I know these results are extremely uncomfortable, and most people, including myself, just wish they weren't true. But this is what the data tells us.

We hear that vaccines save millions of lives, as Pierre Corri said in Wisconsin, and anyone that tells you that COVID vaccine saved a million lives. It's ridiculous. This vaccine saved no one. In fact, what we are seeing now through DTP is there's vaccines that cause more death. What is what she ends up saying is if we remove DTP vaccine from the program, we will save a million children a year. Okay? Did you hear that? Not if we add a vaccine by removing a vaccine, we will save a million children a year. So I say all this because you see how hard this is for these scientists to, and it's, admit. And they're saying, you may think we know how the vaccines work, but we do not. This is the statements they're making. This is what I can. And the work that we've done is proved over the last

several years through multiple lawsuits and everything else. All right. Now that you understand that, that a vaccine is only looked at by those that make it, does it stop the illness? They never look at does it actually make you healthier in the long term? Or does it raise, increase your risk of death for autoimmune disease and things like that? Now let's go back to this story that caught my attention. Now that we're looking at this way, one baby dies and eight other spight for life due to spike in usually harmless virus. It tells us the sudden spike in the condition left health officials baffled and investigations began launched to determine the causes of the spread. And baby dies and nine more admitted to hospital than usual cluster of heart infections. Late on Tuesday night,

the World Health Organization said there had been a rise in severe myocarditis of potentially deadly inflammation of the heart in newborns and infants between June 2022 and March 23. A total of 15 babies, 10 in Wales, 5 in England, presented with a condition during this period, WHO said, of these nine tested positive for an enterovirus. Oh, an antivirus is the cause. A common pathogen which can cause respiratory illness, hand, foot, and mouth disease, and viral meningitis. In very rare instances, young babies can develop myocarditis. Oh, so this virus can cause myocarditis, I guess. The report incident represents an increase in both the number and severity of enterovirus infections in infants under the age of 1. month. The WHO said in Tuesday's announcement, only one case had been identified in Wales in the six

years prior to 10 cases appearing in Wales in one year last year. Okay, massive increase, and they're blaming it on enterovirus. So let's check in here. I know we're getting the weeds, but stay with me. Myocarditis, where do we hear that before? We know that that was a side effect of the COVID vaccines. It's one of the most, you know, the one that got the most press. because they couldn't get around it. Now all of a sudden it's happening to infants. It couldn't possibly be the vaccine in their minds. It's an enterovirus.

Let's look at their investigations into antivirus and why are they looking at it? When we look at enterovirus studies, this is what they say, the suppression of the tolek receptor 7 dependent type 1 interferon production pathway by autophagy, resulting from enterovirus 71 and Coxacivirus A16. These are the hand, foot, and mouth disease. We all hear about infections facilitates their replication. I just want you to pay attention this toll-like receptor part. Enterovirus 71 Coxack E-16 is the primary agents causing hand-foot and mouth disease.

These findings suggest that an increased EV-71 A-16 replication may lead to suppression of the toll-like receptor 7-mediated interferon-1 signaling pathway. So it's suppressing this whatever this toll-like receptor is. There's more headlines on this enterivirus. This is all going to, I'm going to sum this up, it'll make perfect sense. And now we're talking about Toll-like receptor 3. Before it was 7. Now it's 3. Same thing related to enter a virus.

So it seems to be suppressing these toll-art receptors. There's another article. It goes on and on and on. I can show you all these articles on enteroviruses suppressing toll-like receptor 7, 3, 4. Where have you heard this before? If you've been watching the high wire, you would know that the COVID vaccine was designed to suppress your toll-like receptors, specifically 7. three, four, why? Here's why. Because when they were trying to make these MRI vaccines, right, they were taking this foreign mRNA protein, injecting into people's bodies. They wanted to get

to your cell, this spike protein, so it can make your cell into a virus manufacturing plant. The only problem is once this RNA went into your body, your immune system, because of these tole-like receptors, by the way, the tolech receptors are like the centurions, right? The guardians of the guardians of the gate of your white blood cells. They're the ones that notice that there's a foreign invader, a cancer cell, or a virus, or a bacteria, and they call in the warriors and say, kill it dead, it's attacking our body. These are your centurions, right? Your toll-like receptors. Well, these toll-like receptors were noticing the RNA being injected in the vaccine and attacking it, so it couldn't get to the cells. So the geniuses that made the vaccine said, you know what, it would be

great if we could put your tolleck receptors to sleep. Here's the geniuses, doctors Drew Weissman and Catalin Carico brag that they were able to replace the pseudo-uridine in this spike protein, in the DNA, put a, you know, basically mutate it so that it would go into the body and put the tolech receptors to sleep so that, wow, they were sleeping, it could invade your cells and turn your cells into a vaccine manufacturing plant. Here's an article that was written about it, stabilizing the code. It goes on to say in 2005, Dr. Weissman and Carrico discovered a way to protect for an MRNA from the body's immune system.

That scientific milestone would be key to the advancement of the MRNA vaccines in 2020. Their key discovery that by modifying the RNA code using a nucleoside uridine resulted in ablating the innate immune response involved toll-like receptors. How does that simple removal of one letter of code from MRNA achieve that? It does so by affecting toll-like receptors, the alarm signal the innate. The key toolite receptors affected that they bragged about are TLR3, TLR7, tolect receptor, and toelike receptor 8. They act as centuries whose job is to recognize foreign invaders by way of other forms of patterns. So they have changed this virus as it enters your body.

Now let's put this all together. We are hearing that we have a rise of myocarditis amongst infants. All of medicine is looking at the enterovirus, which used to not be a problem. it very rarely caused myocotitis, but now it is. And what we know about it is it tends to limit your tolect receptor 7 and 3. Do you see how this works? Wait a minute. Did mom while pregnant just get a COVID vaccine?

Did we just do what the DTP vaccine did? Did we protect you from diphtherous and tetraudus or produces? Or maybe in this case, we know the COVID vaccine didn't protect you, but that was the idea. But has it made your baby vulnerable to other illnesses and enter a virus that used to be mild is now causing myocarditis. With the DTP, a case of dysentery used to be mild, now it's killing kids at 10 times a rate. This is how this whole program works, and this is the problem with the vaccine program. And let me explain to you when you're trying to look at the experts, we're all saying, well, what are the experts doing? Here's what the experts are doing. This is what

they've got going on. They're working for pharma, okay? They have got the bottles of medicine in their way. So they cannot. They're saying, well, I don't know what's causing the inflamed hearts. It doesn't recollect to them in any way that it was actually a vaccine that was causing this problem. It couldn't be the vaccine because they can't see it. No, they're looking at viruses. They're like, no, it's got to be a virus. It's got to be intra-virus. And this is how the entire program works.

They cannot see the elephant in the room because they got these freaking Coke models on their eyes. This is what's going on. They just took it off, took pharma out of the discussion. They go, oh, my God, wait a minute. You know what I just realized? The vaccine we just gave most of the world actually is. suppressing tolect receptor seven and three and four, and maybe that is what's causing myocarditis in these children. Maybe that's why this enterivirus that was once mild is now freaking deadly.

Go ahead. Keep trusting these fools. But stop watching the high wire because we'll never do it. We'll never join you. All right. There's my little lesson. I hope that makes some sense. You cannot trust the experts any longer. They're funded by pharma. Everything they do, sure that they do not look at the elephant in the room, which was the last product that pharma made. And guess what they will do with the enter virus? They'll come up with the vaccine for it. So the solution to the problem the vaccine probably caused is another vaccine. If you want more information like this, if you want us to keep having the, you know, legal attacks that are helping us win against the FDA, the NIH, CDC, and able to bring

you this information so clearly, we need your help. Obviously, we're being censored. I'm on billboards at least Wikipedia and all over the internet, saying that I'm spreading misinformation, but I know you don't care. Instead, you want to help us do our work because we're the only ones telling you the truth. Please become a recurring donor. It makes it possible. We have science we want to do. I want to start funding good science. I want to open up a laboratory because we have got to get the scientific method. It's on a ventilator right now. It's being given remdesivir, and the scientific method is about to die. and only I can is in here fighting an FLCCC also through Pierre-Cori,

but it's groups like ours that need your help.