The Real Reason They Want to Give COVID Jabs to Kids. “Vaccine Makers Want Zero Liability”

“The reason they did 16 is because 16- and 17-year-olds are still on the children’s vaccination schedule. And then the manufacturer gets full liability protection.”

This article has been cross-posted from globalresearch.ca

Original article written by Dr. Joseph Mercola and Alix Mayer
on Mercola 9 January 2022

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The reason our children are being targeted by COVID mandates is because vaccine makers want to get the shots onto the childhood vaccination schedule.

Once a vaccine is added to the childhood schedule, the vaccine maker is shielded from financial liability for injuries, unless the manufacturer knows about vaccine safety issues and withholds that information

Products must satisfy four criteria in order to get emergency use authorization:

    1. There must be an emergency;
    2. a vaccine must be at least 30% to 50% effective;
    3. the known and potential benefits of the product must outweigh the known and potential risks of the product;
    4. and there can be no adequate, approved and available alternative treatments (drugs or vaccines). Unless all four criteria are met, EUA cannot be granted or maintained

According to a U.S. federal court decision, the Pfizer shot and BioNTech’s Comirnaty are not interchangeable

Comirnaty is not fully approved and licensed. It’s only “ready for approval.” Comirnaty is licensed to be manufactured, introduced into state commerce and marketed, but it’s not licensed to be given to anyone, and it’s not yet available in the United States. They’re waiting for it to be added to the childhood vaccination schedule, to get the liability shield

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In this interview, Alix Mayer explains why our children are being so aggressively targeted for the COVID-19 injection even though they’re not at risk of serious SARS-CoV-2 infection, and clarifies the status of Comirnaty.

Mayer, board president of Children’s Health Defense — California Chapter, is herself vaccine injured; not from the COVID jab, but from a series of vaccines she received 20 years ago. (Incidentally, Mayer grew up in the Oscar Mayer family in the 5th generation descended from the original Oscar Mayer, a German immigrant who started as a butcher boy. Despite Mayer’s vaccine injury, her family does not share her views on vaccine safety issues.)

Mayer graduated from Duke University with a BA and from Northwestern University with an MBA in finance and management strategy. She worked for Apple in the mid-1990s. When she was 29, Apple promoted her to acting manager of worldwide customer research.

In preparation for a family trip to Bali, her doctor recommended getting six vaccines: hepatitis A vaccine, hepatitis B vaccine, diphtheria, tetanus, polio and oral typhoid, which she did. Eventually, 13 years later, she finally realized it was these shots that triggered her health problems.

“They gave me brain damage and total disability,” she says. “I spent three years in my early 30s being 80% housebound, and I really I didn’t know if I was ever going to get better.

I went through a whole bunch of diagnoses: lupus, chronic fatigue syndrome, Lyme disease. Ultimately, none of those made sense and none of the treatments made me any better, until we put the pieces together and figured out that I was actually vaccine injured.

It’s literally just a cause and effect. If you look back at my history and lay out my vaccine schedule, you can see that my health declined two weeks after I got the vaccines.

I had encephalitis and encephalopathy … digestive issues, hypersomnia — sleeping 16 hours a day — flu-like symptoms, a 24/7 migraine, joint pain. I really had no life at all in my early 30s until I went on a gluten-free diet. That started my health recovery.

I then became an award-winning medical journalist with a bunch of different blogs, and then a health consultant. In 2018, I retired from all that and joined Children’s Health Defense.”

The COVID Jab Tragedy

While many vaccines have a questionable safety profile, especially when combined, data from the Vaccine Adverse Events Reporting System (VAERS) suggest there’s never been a vaccine as dangerous as the experimental mRNA gene transfer injections for COVID.

What’s more, while lack of transparency and accountability has been a chronic problem within the vaccine industry, the obvious hazards associated with vaccines are really being highlighted by the COVID jabs.

Many now know of someone who has been injured by the COVID jab, and most were injured so shortly after the shot that it’s hard to deny a correlation. The staggering number of injuries reported among adults who have received the COVID shot in turn highlights the insanity of rolling it out to young children.

According to Mayer, the reason they’re trying to mandate the COVID shot for children is to evade liability for injuries, because once a vaccine is on the childhood vaccination schedule, vaccine makers have immunity against lawsuits for injuries.

Vaccine Makers Want Zero Liability

The COVID shots currently have legal immunity against liability because they’re still under emergency use authorization (EUA). If you think BioNTech’s Comirnaty has been fully licensed, you’d be mistaken. Mayer explains:

“I put together a slide deck about Emergency Use Authorization (which you can see in the video interview above) because there is so much confusion over this and what’s really going on. Once you understand the genesis of EUA and the standards they have to meet in order to keep these products on the market, then you understand the behaviors [we’re now seeing].

They’re falling all over themselves to protect the EUAs for these products and also introduce other very confusing kinds of approval to get away with stuff. So, let me just start to clarify it right now.

This presentation is all about these three strangleholds that the vaccine makers and our government are never going to let go of … These are the things they’re guarding with their lives.

First of all, they need to guard the emergency … so they cannot have any early treatments. Those cannot exist. They’re also going for full liability protection, and children will be used as pawns to get them full liability protection.

Vaccine makers love EUA products because they have this huge liability shield. If you’re injured by an EUA vaccine, you can’t sue the manufacturer, you can’t sue the person who gave it to you, you can’t sue the institution where you got the shot.

You have to go through something called the CICP, the Countermeasures Injury Compensation Program, where they’ll only cover unpaid medical expenses, and probably only for pharmaceuticals and lost wages.

Now, if you’re vaccine injured, let me tell you right now, you are not going to be using pharmaceuticals because they do not work for vaccine injury. They will make you sicker. You’ll be on two dozen pharmaceuticals before you know it and you’re going to be sick from those. They do not work. The only thing that’s going to get you better if you’re vaccine injured is natural treatments …

That’s the kind of treatment you’re going to need, and that’s not even covered, even if you were to get compensation. Everybody I know with chronic illness, whether it’s a child or an adult who has chronic fatigue syndrome, vaccine injury, Lyme disease, they’re paying $50,000 out of pocket per year.

If you can’t work and you have to pay for your treatment out of pocket, I don’t know how you ever get by. People suffer like crazy, they lose homes, they go into bankruptcy.”

Since its inception, the Vaccine Injury Compensation Program (VICP), which pays for injuries caused by vaccines on the childhood vaccination schedule, has paid out about one-third of claims. It’s a long, arduous process that oftentimes takes years and in the end rarely provides adequate compensation.

“If you do end up getting compensation … they don’t pay it out in one lump sum, they pay it out year by year, and they pretty much hope that whoever is injured is actually going to die of their injuries before they get compensated.

That’s been said to me a bunch of times by people who’ve been through this horrible process. Now, the CICP has only compensated 3% of claims. And so far, there have been no approvals for [compensation] for COVID shot injuries,” Mayer says. [Editor’s note: The first COVID case was recently determined “eligible” for compensation, but the case has not yet been adjudicated.1]

Stages of Liability: EUA

In her slide show, Mayer reviews each of the stages of product liability, and whether the mRNA shots can be mandated. As mentioned, vaccine makers have no liability as long as their product is under EUA, as the product is investigational.

“Investigational is a synonym for experimental,” Mayer says. “And the word experimental ties it directly into the Nuremberg Code, which says that we cannot be experimented on [without consent]. We always have the right to accept or refuse a medical treatment.

[The Nuremberg Code] is not a law, but it’s a code under which the whole world is supposed to be operating by. And it is actually codified into some local and federal laws as well … So, what everybody needs to know is that coercion and duress are considered de facto mandates and illegal. De facto means that it’s basically the same as an outright mandate.

It’s illegal medical segregation, medical apartheid [because that is a form of coercion or duress.] So, if you go to a restaurant and they demand your vaccine passport, only let you eat outside, and they might not let you use the bathroom, that’s medical segregation.

That is illegal and I do not support businesses that do that and you shouldn’t either. Any access privileges that are different between the vaccinated and unvaccinated are illegal, and any visual indication of vaccine status like a sticker or a bracelet … that’s also illegal because that creates segregation and medical apartheid, [since they are all forms of coercion or duress.]”

Importantly, mass violation of the law does not make something legal.

“If we all drove 100 miles an hour on Interstate 80, would we watch the speed limit signs suddenly changed to 100 miles per hour? No, it’s not going to happen. Mass violation of the law has never made anything legal. And just because schools and businesses and our government are mandating these shots, it doesn’t make it legal. It’s all illegal …

Now, they know full well that it’s illegal to mandate these [COVID shots]. President Biden knows it’s illegal. But what they’re counting on is that the court cases overturning their illegal mandates will take a while, and in that interim, people are going to be scared enough to get the shots. And unfortunately, it’s worked.”

Stages of Liability: Full Licensure and Childhood Scheduling

The next stage is full licensure (FDA approval). Once a product is fully licensed, the company becomes liable for injuries. At that point, the product can be legally mandated. Of course, knowing how dangerous the COVID shots are, no manufacturer wants to be financially liable for injuries. They’d be sued out of business.

This is the holy grail if you’re a manufacturer of a COVID vaccine right now. You want it to be fully licensed, but not put on the market until you get it on the children’s schedule. ~ Alix Mayer

To get immunity against liability again, the vaccine manufacturers need to get their product onto the childhood vaccination schedule. This will also allow government to mandate the shots. As noted by Mayer:

“This is the holy grail if you’re a vaccine manufacturer of a COVID vaccine right now. You want it to be fully licensed, but not put it on the market until you get it on the children’s schedule.”

DOJ Redefines Medical ‘Consequence’

In Doe v. Rumsfeld,2 the court held that service members could refuse an EUA product without punitive consequences such as dishonorable discharge or other punishments. Therefore, there were no consequences to refusing an EUA product, other than the natural consequence of possibly getting the disease.

However, in July 2021, the U.S. Department of Justice attempted to redefine the term “consequences” just for the COVID shot, to suggest that punitive consequences, like job loss or being separated from your working or learning location, are legal when a person refuses an EUA vaccine.

“But this type of consequence, a punitive consequence, has never been adjudicated,” Mayer says. “That’s not in any law. This is just an opinion from the DOJ. And it absolutely means nothing, except it came from our DOJ, so people give it a lot of authority.

They also stated twice — and this is so hard to understand because it’s just beyond reason — that the right to accept or refuse an EUA product is ‘purely informational.’

Literally, you can read that you could die by taking it, but it’s purely informational. You cannot act on it. That’s what the DOJ says. Again, it’s not adjudicated, so it doesn’t mean anything. It’s an opinion. It holds no legal weight at all. So, as we said before, these mandates are starting to be overturned.”

Four Standards for EUA

There are four standards that must be fulfilled for an EUA. If any of these criteria are not met, EUA cannot be granted or maintained. First, the secretary of Health and Human Services has to declare and maintain a state of emergency. If the emergency were to go away, all EUA products would have to come off the market. And that doesn’t just mean vaccines. It also includes the PCR tests and even surgical masks.

The second standard is evidence of effectiveness. Historically, vaccines had to show a 70% or greater effectiveness, as measured by a fourfold increase in antibody levels, in order to qualify. For an EUA vaccine, the efficacy threshold is only 30% to 50%. In another departure from prior vaccine approvals, the COVID vaccine clinical trials relied on the RT-PCR test, not antibodies, to demonstrate effectiveness in the small “challenge phase” of the trials.

Now, you probably heard that the Pfizer shot was 95% effective when it first rolled out, but that was relative risk reduction, not absolute risk reduction. Confounding these two parameters is a common strategy used to make a product sound far better than it actually is. The absolute risk reduction for Pfizer’s shot was just 0.84%.3

For example, if a study divided people into two groups of 1,000 and two people in the group who didn’t get a fictional vaccine got infected, while only one in the vaccinated group got infected, the relative risk reduction would be reported as 100%. In terms of absolute risk reduction, the fictional vaccine only prevented 1 in 1,000 from getting the infection — a very poor absolute risk reduction.

The take-home message here is that even though the minimal threshold for effectiveness is ludicrously low, in terms of absolute risk reduction, these shots still don’t measure up. Within six months, even the relative risk reduction bottoms out at zero. What’s more, there’s evidence that the clinical trials were manipulated as well.

“I remember an analysis very early in lockdowns [that showed] if you added back all the probable cases of COVID to the clinical trial [data], the effectiveness went from 90% to between 19% and 29%,”4 Mayer says.

The third standard is that the known and potential benefits of the product must outweigh the known and potential risks of the product. In the case of COVID shots, there’s overwhelming evidence showing they do more harm than good.

The fourth and last standard that must be met is there can be no adequate, approved and available alternative treatments (drugs or vaccines). “This is why hydroxychloroquine and ivermectin were quashed,” Mayer says. This is also another reason Comirnaty is not treated as a fully approved product in the U.S., because if it were, then all the other COVID shots that are under EUA would have to be removed from the market.

“This is a four-legged stool,” Mayer says. “If any one of these legs goes away, you have to take your EUA products off the market … by law. I put [state of] emergency and [treatment] alternatives in red, because those are two of the things that they have a stranglehold on; those are things they are guarding like crazy.

This means that every variant that comes out, they have to make it sound super scary to keep the emergency going. So, the variants serve a purpose. You have to think about these variants in the context of this crime, where they have to keep the emergency going to keep their products on the market.

You would think this emergency would stop maybe when we get to herd immunity, maybe if we get 90% vaccination uptake, maybe COVID is just going to go away, like smallpox did in the early 1900s [even though] only 5% of people were vaccinated. [But it won’t] go away [until] the shots get full approval and the manufacturers get a full liability shield.”

Comirnaty’s Quasi Approval

With regard to Comirnaty, is it or is it not fully approved and licensed? The answer is more complex than a simple yes or no. Mayer explains:

“Comirnaty’s quasi approval is just for BioNTech. It doesn’t have to do with Pfizer, and this is why I’m doing this presentation because I’m going to explain what’s going on with that.

This is the race to get liability protection. Remember, that’s the other stranglehold that they want. They really want to get this liability protection. Once the COVID shots are fully approved, the manufacturer has full liability.

There’s all this confusion about Comirnaty. Was it fully approved? Is it on the market? Is it interchangeable with the Pfizer shot? And does it make the COVID shot mandate legal? It’s all the same answer. No, no, no, no.

The FDA issued an intentionally confusing biological license application approval for Comirnaty. It was an unprecedented approval to both license the Comirnaty shot, saying it’s ‘interchangeable’ with the Pfizer shot. But they also said it’s ‘legally distinct.’

In that same approval, they retain the vaccine’s liability shield by designating it EUA as well. They want it to be fully approved, but they want the liability protection, so they did this BS dual approval.

So, [Comirnaty] is licensed to be manufactured, introduced into state commerce and marketed, but it’s not licensed to be given to anyone, and it’s not available in the United States. It’s available in the U.K., New Zealand and other places, but it is not available in the United States because they’re really scared of liability.

Now, are you ready for this one? The BLA actually states that Comirnaty is only ‘ready for approval.’5 It doesn’t say it’s approved anywhere in the document. And they buried this language in a pediatric section to confuse people even more.

Here’s what they said; ‘We’re deferring submission of your pediatric studies for ages younger than 16. For this application, because this product is ready for approval for use in individuals 16 years of age and older, as pediatric studies for younger ages have not been completed.’

Why did they do this? Sixteen is a very important number. You would think the age break would be 18. That’s a very typical age break for everything else that we do in this country. Why 16?

The reason they did 16 is because 16- and 17-year-olds are still on the children’s vaccination schedule. And then the manufacturer gets full liability protection. That’s why this is ready to be approved for 16 and up, not 18 and up.”

Comirnaty Is Not Fully Licensed

This confusion is clearly intentional. On the one hand, the FDA claims Comirnaty is interchangeable with the Pfizer shot, yet it’s also legally distinct. Courts have had to weigh in on the matter, and a federal judge recently rejected the DoD claim that the two shots are interchangeable. They’re not interchangeable. That means Comirnaty vaccine is still EUA. It doesn’t have full approval and it’s not on the market.

“Military members involved in lawsuits are challenging the military’s COVID vaccine mandate. They filed an amended complaint seeking a new injunction after the judge last month rejected the assertion that the Pfizer COVID shot and BioNTech’s Comirnaty are interchangeable. So, we’re still hammering on this legally, but a court has ruled that they’re not interchangeable.

[Editor’s note: This information is accurate at the time of the interview, but legal challenges are ongoing and courts may issue new rulings. December 22, 2021, the U.S. Supreme Court announced6 it has slated January 7, 2022, to hear arguments challenging Biden’s vaccine and testing mandates.]

So, how do we know that Comirnaty is not being treated as fully approved? First, the approval states you have the right to accept or refuse the product. That means it’s an EUA. Second, it’s not available in the U.S. because Comirnaty doesn’t have liability protection. Third, if it were available, it’s an alternative [treatment] and all other EUA shots would have to come off the market.

No. 4, the CDC Advisory Committee on Immunization Practices (ACIP) would have to recommend it for ages 16 to 18 and the CDC would have added it to the children’s recommended schedule. That’s how we know it’s not fully approved and on the market.

Here is the label for Comirnaty. It says it’s emergency use authorization. It doesn’t say it’s fully approved, because it’s not. But look at the safety information they are recognizing: Myocarditis and pericarditis have occurred in some people who’ve received the vaccine, more commonly in males under 40 years of age than among females and older males.

So, this is saying that young men are getting heart inflammation. And what we know from all the anecdotal reports is 300 athletes have died or collapsed on the field, and children in schools have died of heart attacks. That’s what’s going on here.

And the reason they have to declare this is because they know it. They know it’s happening. And the only way they can be sued is if they know there’s a problem with their vaccine and they don’t declare it. So, they declare it here, in very mild language as if it’s not that big of a deal, but it’s a very big deal. Young people are dying [from the shots] who have a 99.9973% chance of recovering from COVID …

The holy grail is to get the shot on the CDC recommended schedule for children, because then it gets full liability protection according to the 1986 Act. This is why they’re going after our children when they have a 99.9973% recovery rate …

Every medical intervention is a risk benefit equation, and it doesn’t calculate for kids at all. They should never be getting COVID shots. The shots don’t prevent transmission. They don’t prevent cases. They don’t prevent hospitalization or death.”

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Notes

1 Reuters October 19, 2021

2 Biotech Law December 22, 2003

3 Maryannedemasi.com November 11, 2021

4 The BMJ Opinion

5 FDA BioNTech BLA Approval

6 USA Today December 22, 2021

NOTE FROM EXPANDING AWARENESS RELATIONS:

How egregious that the big pharmaceutical companies are trying to use children as a liability shield to protect their criminal organization. Even worse, however, are the governments/politicians and health officials/institutions that are letting them. No amount of “contracts” should ever protect criminal activity, which is what we’re seeing right now in what is quite possibly the largest racketeering scandal in the history of humankind.

(And in my opinion, this isn’t even covering the ACTUAL REAL reason that they want to vaccinate children so much. This is only the watered-down, “scientific”, realistic version…)

Any documents/legal dealings (keyword here: LEGAL – although, what does that matter when corrupt enterprises are able to re-define terms according to their purpose?) and NDA’s should automatically become null and void if there is fraudulent activity happening.

However, when those “in charge” are allowed to investigate themselves, they, of course, end up finding no wrong-doing. And when there are multiple conflicts of interest, all for the purpose of financial bribery and protecting each other, there needs to be effective systems in place to address this obvious malfeasance.

It would seem, the “law” (and even us, everyday/ordinary people) literally needs to take matters into its own hands, and stop catering to enforcing illegal mandates and nonsensical “policies”. When will they go after the REAL criminals, instead of innocent civilians who are simply trying to defend not only their rights and freedoms, but everyone else’s as well? Including law enforcement?

We all need to pick our side in history. Let’s hope we’re picking the right one.

Tal Zaks, Former Chief Scientist at Moderna, Speaks of Nanomedicine, Personalized Vaccines and Genetic Engineering in 2017

Scientist quote/unquote: “hacking the software of life.”

Tal Zaks, former Chief Medical Officer at Moderna (currently partnering with Orbimed) – gives us another look at their terminology of “hacking the software of life”, i.e. – changing/modifying our genes.

Piggybacking off of Klaus Schwab’s statements that gene-editing changes YOU, not to mention Craig Venter’s (of the Human Genome Project) admission that:

“It’s pretty stunning when you just replace the DNA software in the cell, and the cell instantly starts reading that new software, starts making a whole different set of proteins. And within a short while, all the characteristics of the first species disappear. And a new species emerges from this software that controls that cell going forward.”

Craig Venter of the NIH and Human Genome: Creating Synthetic Life | ” – trying to design what we want biology to do”

– it is clear that, by definition, “rewriting the genetic code” changes what it means to be human – or changes whatever species is being modified. Craig Venter himself says that a “new species emerges from this software”.

So while these doctors and scientists try to sugarcoat these ill-conceived endeavors (even if they were born of good intentions initially… “the road to hell is paved with good intentions”), the attempts at genetically changing our DNA have grave consequences; not only on the physical-molecular level, but on the conscious-soul level as well.

Here, Tal Zaks, in a Tedx Talk from November 2017, specifically mentions vaccines (a total of 17 times in a 10 minute presentation) to administer this genetic-changing software. In addition, he also alludes to collecting DNA in order to make “personalized vaccines”. An endeavor that DARPA is also invested in:

DNA Script Partners with Moderna to Develop On-Demand Vaccines and Therapeutics for DARPA

SOUTH SAN FRANCISCO, Calif., and PARIS | April 27, 2021

[ https://www.dnascript.com/press-releases/dna-script-partners-with-moderna-to-develop-on-demand-vaccines-and-therapeutics-for-darpa/ ]

“Rewriting the Genetic Code” – Tal Zaks (2017)

Source: odysee | @RedPillman | Rewriting the Genetic Code

Full transcript below. Some embellishment has been added for emphasis.

Tal Zaks: “So I started my professional life about thirty years ago as a nurse and the pediatric intensive care unit.

And I remember this one infant, let’s call him Jonathan, who came in really really ill. Seemed to have a rare genetic defect, but in those days, gene diagnosis was still in its infancy so we couldn’t really figure out what’s wrong with him.

And in the years since, as I’ve trained as a physician scientist, we’ve been living in this phenomenal digital and scientific revolution. And I’m here today to tell you that we’re actually hacking the software of life. And that it’s changing the way we think about prevention and treatment of disease.

So here’s all the biology you need to know in 30 seconds. Our body is made out of organs, our organs are made out of cells, and in every cell there’s this thing called “messenger RNA” or mRNA for short, that transmits the critical information from the DNA, our genes, to the protein, which is really the stuff we’re all made of.

This is the critical information that determines what a cell will actually do. And so we think of it like an operating system. And it’s not just in every cell of our body. It’s actually in every cell of every organism of life. It’s the same thing.

And so, if you could actually change that, which we call the software of life, you could introduce a line of code, or change a line of code, it turns out that has profound implications for everything from the flu, to cancer. And I’m going to demonstrate that with three short examples.

Let’s start with the flu. So many of us get a vaccine. What is a vaccine? It is an injection in our arm where we get bits and pieces of the virus; the protein, and that teaches our immune system to recognize the virus and so when we get infected we’re not sick.

Now imagine if instead of giving the protein, we would give the instructions on how to make the protein. How the body can make its own vaccine. That’s an mRNA vaccine.

And here’s what it looks like from the cell.”

Image Source: Tal Zaks / Tedx Talks

“So the traditional approach has protein floating around your cells. An mRNA vaccine approach has the cells themselves in your own body making the vaccine.

What’s more alarming: a stranger prowling the neighborhood, or somebody who’s just broke into your ground-floor, and tripped the alarm?

That’s what happens with an mRNA vaccine. You’re tripped the alarm wire and now the cell is dialing 9-1-1. It’s calling the police at the same time as it’s making the protein and saying, ‘that’s the bad guy’.

That’s how an mRNA works. And for the last several years we’ve shown this actually works in a whole multitude of animal models. Earlier this year we published the first actual study in people. And it actually works in people.

We took a group of volunteers and injected them with a messenger RNA vaccine against a variant of flu/influenza. And all of these volunteers got the immune response we were hoping to see. The side-effect profile was pretty benign, what you would see with any normal type vaccine.

So we’ve proven the principle, this actually can work. It works in people and now we’re going to be developing a whole slew of vaccines against diseases for which we don’t have one. So that’s infectious disease.

Now for the second example, let’s talk for a minute about cancer. Horrible disease. Cancer has affected the lives of many of us and will affect the lives of many more of us as we age.

The problem with cancer at the cellular level is that the DNA is screwed up. You’ve got these mutation on this screwed up DNA, leads up to screwed up information that makes screwed up protein. And so the cell loses control.

Now, how do you figure out what is actually screwed up? Well, you got to figure out the whole sequence, right?

It took us decades and billions of dollars to sequence the human genome, and we’ve done that. We achieved that in 2003. And now we’re less than 15 years later, and it takes us a week. And we can do it for every patient. So now we can go and figure out what exactly is screwed up in a patient, and we can use that information to make a vaccine.

We take that information, say a patient with lung cancer, and we take it – we take the biopsy, we figure out the sequence, we figure out their immune system, we – and that all becomes information. It goes up in the cloud into a bioinformatic algorithm and then automatically makes a vaccine that we administer into their normal tissue; into the muscle to try and wake up their immune system.

Now the challenge, of course, is that every person’s cancer is different. Mutation happened by random chance. And so to do this you have to make it personalized.

So this is me, but if every patient is different, what we’re going to have to do is make a personalized cancer vaccine for every patient. And that’s exactly what we’ve started to do. Every patient gets a vaccine that’s based on the sequence and their own tumor.

So when we started to do this a couple years ago, my CEO stopped by one evening and said, “Tal, I get the idea but is this going to work?” And I said, “Look, Stefan. I don’t know, but we’ve got all the pieces to try and answer the question so we should try.”

And today I can tell you that I still don’t know if it’s going to work. But I know we’re able to actually run the experiment. Earlier this week the first patient was treated with a personalized cancer vaccine we made just for her.

So in the months and years to come we will know the answer of whether we can actually wake the immune system against somebody’s cancer with a personalized cancer vaccine so stay tuned.

I’m gonna finish with a third example of something called “methylmalonic acidemia” or MMA for short. Now the name doesn’t matter. Okay? This is just a disease that is caused by an enzyme that’s critical for metabolism. And children are born and they lack this one crucial gene. And so their body is not able really to fight infection properly or anytime they have any sort of stress, their body goes into crisis. They have one gene that’s gone awry and it causes a really significant disease.

If you look at what happens over time, for these children, about 1/3 of them don’t make it to the age of 10. You see here the survival curve whether the gene is completely lost or whether there’s just an aberration in it, the survival is impaired.

And, what do we do? Well there’s not much you can do because the missing protein is actually missing inside their cells. So what do we do? Well, here’s what we do. We take out their liver and we transplant the liver from a donor that is healthy and normal into these kids.

Think about it. They’re missing one critical piece of information and what we do is transplant an entire organ. Well, it fixes the problem, but what if there’s a better way? What if we could fix the missing information?

So based on innovations, nanomedicine, a new class of invention that Bob Langer across the river at MIT in Cambridge has been inventing, we’re now able to package this information and messenger RNA with a goal of giving it as an infusion, and then having it go to the liver to replace that missing information.

Is this going to work? Well we know the biology works. So together with the National Institutes of Health, we’ve studied this in a mouse model and this mouse has been engineered to have the exact same problem that the kids have. They’re lacking the one – the same gene. And you can see in the red line what happens to these mice when they’re born. Pretty much immediately they die. They cannot cope with stress. But if you inject messenger RNA that codes for the one missing protein that replaces that information, these mice, all of them survive, as you can see in the green line. And if you look at them they not only survive, they’re actually growing, they’re gaining weight, they look like they’re healthy littermates.

We’re hoping to start the clinical trial in the near future and the idea is the same thing here. If you think about what it is we’re trying to do, we’ve taken information and our understanding of that information and how that information is transmitted in a cell, and we’ve taken our understanding of medicine and how to make drugs and we’re fusing the two. We think of it as information therapy.

I started by telling you about Jonathan and 30 years ago, and I was a nurse in the intensive care unit, I worked two night shifts, and Jonathan came in when he was about 12 months old and very quickly became dependent on a ventilator. And for the next 15 months or so, every time I came into the unit he was my patient to care for. You know, bathe, feed, treat, play with – he couldn’t talk, he was on a ventilator, but he was very much alive and you could tell – you could play with him, his eyes would – would follow me. After a while he would recognize me. Until one day I came into the unit for my shift and he was no longer there. He had died because of an infection in between shifts.

Imagine a world where we cannot just diagnose, but we can actually use the information to create vaccines to wake up the immune system to something like cancer and to fix the missing information for children with diseases like Jonathan, so that they can leave the ICU and live a healthy life.

Thank you.”

What is “nanomedicine”?

“Nanomedicine is defined as the medical application of nanotechnology. Nanomedicine can include a wide range of applications, including biosensors, tissue engineering, diagnostic devices, and many others. In the Center for Nanomedicine at Johns Hopkins, we focus on harnessing nanotechnology to more effectively diagnose, treat, and prevent various diseases.”

[ https://cnm-hopkins.org/what-is-nanomedicine/ ]

Interestingly, but not surprisingly, Johns Hopkins was the organization that the WEF (World Economic Forum / Klaus Schwab – famous for the “Great Reset” agenda) chose to moderate the EVENT 201 Plandemic Pandemic exercise, with the help of the Bill and Melinda Gates Foundation…

And while, of course, Mr. Zaks ends his speech high-lighting the beneficial aspects of a “gene-editing vaccine” and reminds the audience that it is to “cure cancer” or any other number of diseases, we must be alert to alternative motives and the implications of what could arise from such technological tampering of the human genome, not to mention a collection of the population’s DNA in a database – to control and alter at their discretion.

Now aside from those chilling prospects, is it worth it to forever alter a human being, and what it means to be human, by injecting them with genetic changing software? What possibilities might arise from such an endeavor? Are we SURE that they have our best interest in mind? (that is a rhetorical question, by the way… because of course they don’t) If they can change us as a species, then it follows suit that it can change our emotions, our thoughts, even our very purpose.

There are some things in life which should not be meddled with. “Life” itself, is definitely one of them.

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 Gerd Altmann from Pixabay

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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