Children are targeted for C-19 vaccines because the vaccine manufacturers what to put the vaccine into the vaccination schedule.
When the vaccine is added to the schedule, the vaccine producer is shielded from financial liability for injuries so that they will make millions every year.
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Alix Mayer explained why the children are targeted for the C-19 vaccine even though they aren’t exposed to the risk of severe consequences from the virus.
Mayer, the board president of Children’s Health Defense, is vaccine injured from a series of shots she received 20 years ago.
She graduated from Duke University with a BA and from Northwestern University with an MBA in finance and management strategy. Previously, she worked for Apple in the middle 1990s; at the age of 29, she got promoted to acting manager of worldwide customer research.
Her doctor recommended her six vaccines: hepatitis A vaccine, hepatitis B vaccine, diphtheria, tetanus, polio, and oral typhoid, which she did. Thirteen years later, she acknowledged that the vaccines caused 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 didn’t know if I was ever going to get better.
I went through a whole bunch of diagnoses: lupus, chronic fatigue syndrome, and 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 layout 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, and 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 C-19 Jab Tragedy
Many shots have a questionable safety profile when combined; data from the VAERS show that there hasn’t been a vaccine as dangerous as this mRNA gene transfer injection for C-19.
The lack of transparency is a chronic problem in the vaccine industry.
Many people know someone who has been injured by the C-19 shot, and most were injured shortly after the shot, and we can’t deny the correlation.
Mayer stated that they try to mandate the C-19 shot for children because they want to evade liability for injuries. Once the shot is on the childhood vaccination schedule, vaccine makers have immunity against lawsuits for injuries.
Vaccine Makers Want Zero Liability.
The COVID shots have legal immunity against liability because they’re still under emergency use authorization.
“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 VICP, which pays for injuries caused by vaccines on the childhood vaccination schedule, has paid out one-third of claims.
“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.
Stages of liability: EUA
In her slide show, Mayer analyzed the stages of product liability and whether the mRNA shots can be mandated.
‘’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 medical treatment.
[The Nuremberg Code] is not a law, but it’s a code under which the whole world is supposed to be operating. 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 statuses 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.].”
“If we all drove 100 miles an hour on Interstate 80, would we watch the speed limit signs suddenly change 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.” She continued.
Stages of Liability: Full Licensure and Childhood Scheduling
The following stage is full licensure. When the product is licensed, the company is liable for injuries. At that point, the product can be legally mandated. Because the shots are dangerous, no manufacturer wants to be financially liable for injuries because they will be sued out of business.
It’s the Holy Grail if you’re a manufacturer of a C-19 vaccine right now.
“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 Redefined Medical Consequence!
In Doe v. Rumsfeld, the court held that service members could refuse a EUA product without punitive consequences like dishonorable discharge or other punishments, so there weren’t consequences to refusing a EUA product other than the natural consequence of possibly getting the disease.
“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 a 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 emergency use authorization.
First, the secretary of Health and Human services has to declare and maintain a state of emergency. If it were to go away, the EUA products would have to come off the market. It includes the vaccines, the PRC tests, and the masks.
The second standard is the evidence of effectiveness. The vaccines had to show 70%+ effectiveness to qualify, but for a EUA vaccine, the efficacy has to be from 30 to 50%./
The Pfizer shot had 95% effectiveness at the beginning. But that was relative risk reduction. 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 one in the vaccinated group got infected, the relative risk reduction would be reported as 100%.
“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.
“This is why hydroxychloroquine and ivermectin were quashed,” Mayer says.
“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 for 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
Mayor explained this:
“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 Isn’t Fully Licensed!
The confusion is on purpose.
The FDA claimed that Comirnaty is interchangeable with the Pfizer vaccine, but it’s legally distinct.
Read below how Mayor explained this:
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.”