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.

CDC, FDA Prepare Mass Distribution of a Merck/Sanofi Six-in-One Vaccine for Kids, Turning Blind Eye to Safety Signals

Egregious oversteps endangering children’s lives.

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The FDA approved Vaxelis in late 2018, but only now is the shot being readied for widespread distribution — in Europe, where infants have been given six-in-one vaccines for years (including Vaxelis since 2016), the vaccines have been associated with reports of sudden infant death.

Since the mid-1980s, the number of childhood shots on the Centers for Disease Control and Prevention (CDC) vaccine schedule has more than quadrupled. When parents express reluctance about turning their little ones into perpetual pin cushions, drug makers and doctors have a ready answer — combination vaccines that “simplify” the schedule by decreasing the number of injections administered.

This month marks the U.S. launch of the Merck/Sanofi joint-venture vaccine, Vaxelis, a six-in-one (hexavalent) combination vaccine that contains diphtheria, tetanus and acellular pertussis (DTaP) components as well as components said to protect against polio, Haemophilus influenzae type b (Hib) and hepatitis B.

Public health officials optimistically believe that bundling all of these components into one shot will help close noncompliance loopholes and increase the likelihood that children will complete “all recommended vaccinations.”

Though Vaxelis is the nation’s first hexavalent injection, it joins other four- or five-in-one vaccines already on the CDC schedule. The U.S. Food and Drug Administration (FDA) approved Vaxelis in late 2018 — as a three-dose series for 2-, 4- and 6-month-old infants — but it is only now, two-and-a-half years later, that the shot is being readied for widespread distribution.

Warning signs were ignored

There are numerous warning signs that potent all-in-one vaccines are too much for immature immune systems to handle. Concerning safety signals have emerged not just for hexavalent but also pentavalent (five-in-one) vaccines.

In Europe, where infants have been given hexavalent vaccines for some years (including Vaxelis since 2016), the formulations have produced many troubling reports of sudden infant death.

Absurdly, none of the clinical studies assessing Vaxelis safety and efficacy conducted fair comparisons against an inert placebo. Instead, in the two U.S. clinical trials for Vaxelis, not only did investigators compare infants receiving Vaxelis to babies who received Sanofi’s five-in-one Pentacel — but babies in both groups also received rotavirus and pneumococcal vaccines at the same time!

In this context, the CDC’s sales pitch to the public — and its claims that side effects are “usually mild” — cannot be considered credible.

Here are some of the other facts missing from the CDC’s communications:

  • In the two U.S. trials six infants died (slide #27) in the Vaxelis group (some after receiving just one dose); one infant also died in the “control” group that received five-in-one vaccines.
  • All six Vaxelis recipients died within six weeks of vaccination. This timing matches other published accounts of infant deaths “clustering” following hexavalent vaccination.
  • The reported causes of death for the infants who received Vaxelis included asphyxia, sepsis, fluid in the brain and sudden infant death syndrome (SIDS). These outcomes correspond to the types of adverse events reported following hexavalent vaccination in Europe.
  • Package inserts for other vaccines on the CDC schedule list similar causes of death, suggesting these fatal Vaxelis outcomes are plausibly associated with vaccination.
  • In the clinical trials, the rate of fever was notably higher in Vaxelis recipients even when compared to children receiving five-in-one vaccines (47% vs. 34%).

Juicing vaccine sales

In the no-liability context enjoyed by vaccine makers in the U.S., combination vaccines are already quite popular. In fact, market watchers and health economists praise the jumbo shots as being a catalyst for positive industry trends and a “key to commercial success.”

 

Thus, financial analysts expect Vaxelis to “garner significant patient share following its [U.S.] launch” — predicting that it will account for almost a third of U.S. DTaP vaccinations by 2028 — or $841 million in annual sales.

These predictions represent good news for Merck and Sanofi, two of the “big four” pharma giants that dominate the childhood vaccine market in the United States. Merck is already doing a booming vaccine business, recently reporting annual sales growth of 14.8% for its pneumococcal vaccine (Pneumovax 23) and 5.4% for its human papillomavirus (HPV) vaccine Gardasil-9.

However, Merck also faces proliferating Gardasil-related lawsuits — including legal actions alleging that the company knew about and ignored life-changing adverse events from the get-go, many of which (when not fatal) have involved autoimmunity and chronic pain. In fact, before the advent of emergency use COVID vaccines (responsible for an alarming escalation of vaccine-related adverse events), Gardasil had had “more side effects reported than all other vaccines combined.”

Sanofi, too, is embroiled in thousands of lawsuits worldwide — notably for its disastrous and sometimes fatal dengue vaccine. As with Merck, this has not dampened overall vaccine sales growth, which continues its strong upward trajectory, likely to be further strengthened by the U.S. Vaxelis rollout.

Although Sanofi has not been a front-runner in the COVID vaccine race, the company is currently running clinical trials for messenger RNA (mRNA) vaccines for both COVID and seasonal influenza.

Aluminum secrecy and grandfathered ingredients

Merck’s proprietary, “super-powered” aluminum adjuvant — amorphous aluminum hydroxyphosphate sulfate (AAHS) — which is believed to play a significant role in Gardasil’s risk profile, is also present in Vaxelis.

After Merck developed AAHS, it began to “preferentially” feature AAHS in its vaccines even though, as Danish scientists outlined last year, the company appears to have disregarded procedures ordinarily required for approval of new adjuvants.

According to the Danes, at the time AAHS appeared, it represented a “new type of aluminium adjuvant with excipients that [had] not been used earlier in [European Medicines Agency] authorised vaccines.” It should have been — but apparently was not — tested against an inert placebo. For this and other reasons, the Danish scientists question the ethical underpinnings of the Gardasil clinical trials.

In noting that Merck also “seems to have prevented independent studies of AAHS,” the Danes repeated a critique aired by world-famous aluminum expert Christopher Exley in 2018. In an extensive discussion of different aluminum-based adjuvants and their immunological mechanisms of action, Exley and co-authors emphasized the importance of studying aluminum adjuvants one by one, as each is “chemically and biologically dissimilar with concomitantly potentially distinct roles in vaccine-related adverse events.”

Concerningly, the Vaxelis liquid suspension is adjuvanted onto not just AAHS, but also another aluminum adjuvant — aluminum phosphate). The package insert disingenuously shorthands the combination of adjuvants as “aluminum salts.”

How this double whammy of aluminum (319 micrograms per vaccine dose) interacts with the vaccine’s six antigens, or Vaxelis’s numerous other ingredients, or the heavy aluminum load in other childhood vaccines is largely unknown.

According to the Vaxelis package insert, the vaccine also includes: polysorbate 80 (an ingredient flagged for its propensity to induce hypersensitivity reactions); glutaraldehyde and formaldehyde (problematic chemicals deemed necessary to inactivate pertussis toxin); bovine serum albumin (often harvested from bovine fetuses when female cows are found to be pregnant at slaughter); three different antibiotics (neomycin, streptomycin and polymyxin B); ammonium thiocyanate (also a rust inhibitor, weedkiller and defoliant); and yeast protein (associated, notably in hepatitis B vaccines, with autoimmune reactions).

Regulatory loopholes allow manufacturers to “grandfather” ingredients into new vaccines if the components are already present in other licensed vaccines — regardless of how inadequate the original safety testing may have been.

Thus, Merck and Sanofi perceived no need to test Vaxelis for DNA-damaging or cancer-causing effects, and conducted no studies of the ingredients’ pharmokinetics (i.e., how the substances move “into, through, and out of the body”).

The main cautionary note sounded in the meager Vaxelis patient information sheet is to not give Vaxelis to children if they are “allergic to any of the ingredients.”

For thee and thee … but not for me?

The CDC seems to be particularly interested in ensuring that poor and non-white children get Vaxelis. The agency began laying the groundwork to offer Vaxelis through the Vaccines for Children (VFC) Program — the agency’s vaccine program for the poor — over two years ago, in March 2019.

In September of that year, the CDC followed up with an affirmative vote. Public health departments have been promoting Vaxelis to participating VFC providers since early June 2021.

At its September 2019 meeting, CDC outlined another topic deemed important for discussion in the near future — raising the issue of whether Vaxelis should be “preferentially recommended” for the American Indian/Alaskan Native (AI/AN) pediatric population.

The tenuous rationale, according to the meeting notes, was because, “in the pre-vaccine era” (more than 35 years ago), “Hib disease occurred at a younger age among the AI/AN population compared to the general population.”

Wave of the future?

Judging from its website, the CDC perceives combination vaccines to be the wave of the future, and has signaled its strong endorsement of Vaxelis by incorporating the new vaccine into its 2021 vaccine schedule.

As if exposure to six antigens were not enough, FDA and CDC also say it is okay for healthcare providers to administer the six-in-one shot at the same time as other vaccines.

These agencies’ characterization of the Vaxelis safety profile as “acceptable” indicates they have either not done their due diligence, or are willing to accept a high level of collateral damage in exchange for the “convenience” of six-in-one shots.

However, as the “overwhelmed by guilt” parents of COVID-vaccine-injured teens are increasingly finding out, convenience is poor consolation for life-changing or life-threatening adverse outcomes.

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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.

Get an Earful

DARPA BRAIN Initiative – Inhumane Experimentations Using Fusion Centers and Electromagnetic Fields to Control & Torture People - "If they want to experiment on you, by the thousands, they will. And you can be driven to insanity and death"
The “FEW” Involved in the “WEF” | Davos and the Purloined Letter Conspiracy. Klaus Schwab’s “Global Leaders of Tomorrow” - "A conspiracy like this could never happen because 'too many people would be involved'." ...
Senator Ron Johnson’s “A Second Opinion” Panel: Renowned Doctors and Medical Experts Discuss Medical Tyranny and Vaccine Injuries/Deaths (Highlight Video – FULL TRANSCRIPT) - Dr. Pierre Kory: "And that’s what I wanted us to be clear that we’re calling attention to today. This is corruption! Plain and simple, it’s corruption!”

Serge Monast and Pierre Gilbert Warned of Mind Control Vaccines in the 1990’s

And more ties to freemasonry.

I am honestly not trying to make deliberate connections from anything I research to freemasonry specifically.

However, I realize that this might have a very synchronous meaning in that the subjects that I am interested in uncovering, just so happen to lead to the same place – and that is freemasonry.

My last post, re-blogged from The Narrow Gate, dealt with pastor Billy Graham since a previous post I made mentioned Franklin Graham and his (incredibly misguided – or perhaps even intentional) advice that Jesus Christ would have wanted us to take this covid vaccine. This was such an obvious attempt at manipulation and deception, that I felt the need to investigate the Graham family further. I wish I could say I was surprised to see that there was a huge relation to freemasonry, but sadly, I was not.

The next item on my list to research further, is the liquid crystal phenomena since I referenced it from my post Magnets/Quarters Sticking to Arms and the connection to vaccines that Pierre Gilbert made in 1995. Which, after checking out the full speech that Pierre Gilbert made, was quite astonished that he made many references to freemasonry as well.

Thus, again, my research somehow leading me to freemasonry again with studying liquid crystals and it’s relation to the vaccine. Again, it is not my purpose to intentionally seek out this correlation. It is just, almost without fail, leading me in that direction. Does everything have a purpose? Is there a reason that this mysterious secret society is turning up in almost every major agenda that is being perpetrated behind the scenes?

Even Anthony Fauci, the talking head of the whole “coronavirus”/”vaccine” agenda has been seen (a couple of times, at least) implementing the hidden hand gesture that is a favorite of freemasons to signal to each other.

The implications of these situations are quite numerous to just be mere coincidence. When one delves deep into many of these occurrences and the organizations behind dictating a global dominance, the path becomes conspicuously clear.

Enter in Serge Monast and Pierre Gilbert

I’ve already done a topic on Serge Monast’s famous Blue Beam Project disclosure, which you can read here: Blue Beam Project: What is it?, but lo and behold when I realized that he has also mentioned liquid crystals in relation to the vaccine – just like Pierre Gilbert did in 1995.

English subtitles:

“In the biological destruction there are the organized tempests on the magnetic fields. What will follow is the contamination of the bloodstreams of mankind creating intentional infections. This will be enforced via laws that will make vaccination mandatory. And these vaccines will make possible to control people.

The vaccines will have liquid crystals that will become hosted in the brain cells, which will become micro receivers of electromagnetic fields where waves of very, very low frequencies will be sent. And through these low frequency waves people will be unable to think, you’ll be turned into a zombie.

Don’t think of this as an hypothesis… this has been done.” – Pierre Gilbert (1995)

Here is Serge Monast’s testimony, 2 years earlier on the liquid crystal vaccines:

The journalist asks: “Do you have other files that you have looked through?”

Serge Monast: “Yes, there is the dossier that I am starting to write next week, and it is a dossier which concerns vaccines, experimental military medicine and liquid crystals.

It’s because I was talking about the different developments in military research produced by the CIA in the United States in terms of vaccines and things like that. And I said listen, it appears from the surveys and results obtained to date that it is possible

It is possible to administer a vaccine, inside of which there does not appear to be anything apparently and which is not offensive to health, in any way.

But on the other hand, the same vaccine, because of its ill-defined content, put in relation a year or 2 years later with another vaccine, which too, seems harmless at first sight, But, the two combined together will produce implausible problems.

And I recently knew that it was possible, without this being necessarily detected at the level of scientific analysis, that it was possible to cut in half a liquid crystal, to put part of it in a vaccine, and a year or 2 years later, the second part is found in another vaccine. The combination of the two, with the information I have at the liquid crystal level, allows the control of individuals, via satellite in order to arrive, at some point, in absolute political control over populations.”

What are these “liquid crystals” that Gilbert and Monast claim will be put into vaccines to control the population?

Here’s one interesting link, that may or may not have anything to do with the predictions of Gilbert and Monast, but is very interesting and relevant reading in any case, and may provide answers as to what these “liquid crystals” can do:

“Living liquid crystals are an example of materials that can act on their own. In nature, these materials are responsible for the motility of cells. Proteins within the cells “walk” along the surface of polymer molecules and exert a force that causes displacement and motion.

“There is a lot of interest in these materials because they are complex, beautiful and relevant,” said de Pablo, vice president for national laboratories. “But we want to understand just how motion and transport are generated within them.”

In the lab, one way to create an autonomous material like this is to combine a liquid crystal with bacteria, which then cause disorder among the liquid crystal when they move.

To study how the material becomes active, the researchers combined swimming bacteria with a liquid crystal in two formats: near the bottom surface of a drop suspended from a needle attached to a glass slide, and in a thin, freestanding film.

Though the bacteria and liquid crystal were initially aligned through a magnetic field, when the field was turned off, the bacteria began to move on their own,” –

“Now we truly understand how this process works, which will ultimately lead to controlling how this material behaves.”

Prof. Juan de Pablo

Controlling crystals for future technologies

The researchers hope to use this information to be able to fully control these living liquid crystals. That would allow them to eventually create a new kind of microfluidic device that transports fluids autonomously without pumps or pressure, or to create synthetic systems that resemble cells and that could move autonomously from one place to another.

“We have a real possibility to control these materials and use them for interesting new technologies,” de Pablo said.”

Source: Scientists harness bacteria to create ‘living’ liquid crystals (2019)

Hm… it sounds eerily similar to what Mr. Monast and Mr. Gilbert have been talking about OVER 20 YEARS AGO.

Now, I want to mention one other name that both Serge Monast and Pierre Gilbert mentioned in at least one of their speech.

Texe Marrs.

It’s strange that both Monast and Gilbert referenced this man. Perhaps because they realized that Mr. Marrs was speaking about many truths, though we may not want to believe him. Yes, his material is highly controversial, and that’s the point. Some of the conspiracies he proposes are so far beyond a normal human being’s willingness to comprehend, that some will just automatically dismiss his statements as that coming from a madman. And THAT’S WHY whistleblowers are so hard to believe in a lot of instances. It is OUR unwillingness to believe that something so sinister and evil could possibly ever take hold on our planet and in the hearts of men.

People, these evil and wicked tendencies have been here since the beginning of humankind. One could debate as to the true origin of where it came from or from what it was created, but there is EVIL in the hearts of men and the sooner we realize that, the better we can understand where this agenda to control the whole population comes from.

And when people are consistently revealing that the organizations behind these heinous plans all seem to come from the freemasons, and their history goes back as far back to Nimrod/Babylon and perhaps even further beyond that, and their animosity is aimed towards Jesus Christ – inverting everything that is holy to that of sin and wickedness – then perhaps we can finally set aside our own pride and ego, and REALLY start listening to these brave people trying to expose these malevolent societies/industries.

Deadly Vaccines of the New World OrderTexe Marrs
Is Freemasonry the Very Synagogue of SatanTexe Marrs

Unfortunate (and suspicious) deaths

Sadly, Serge Monast passed away shortly after revealing these insidious plots, allegedly from a heart complication – and right after he had his children taken away, simply for homeschooling them.

The timing of his death is incredibly ironic; and especially when one considers that Texe Marrs – (who describes initiatives that ARE NOT A “CONSPIRACY THEORY” – the people and groups involved have ADMITTED that this is their goal) – died a few months before this “coronavirus” outbreak in December 2019. Would it be presumptuous of me to assume that Mr. Marrs would be one of the hugest proponents of speaking out against these “vaccines”?

Then when we take a look at the suspicious timing of Mr. Kary Mullis’ death in August 2019 – who most assuredly would have been speaking out against Fauci and the PCR tests – seeing as how Mullis HIMSELF INVENTED THEM – and knew exactly what they were for (and it’s NOT for detecting viruses), and who was also against Fauci, it wouldn’t be a stretch of the imagination to predict that he would be speaking out against this vaccination plan as well.

Hence, why these gentlemen are no longer with us. Am I insinuating that these gentlemen were “killed off” so that they wouldn’t be alerting the public to these highly dangerous and ill-begotten vaccines?

Why, yes. Yes I am.

There’s been a string of highly suspicious deaths that strangely target a key profession in incredibly timed stages:

“You may recall that many months ago there was a spate of bankers dying under suspicious circumstances, while jogging, or “falling” (or being pushed) in front of trains, falling onto piked fences, jumping off of roofs, being shot in their cars, and so on. That pattern of strange deaths followed a spate of similar unusual deaths of so-called “homeopathic” doctors, which followed, years before that, a kill-off of biologists and geneticists, and if we want to go all the way back to the Reagan era, a spate of mysterious and suspicious deaths of high energy physicists.”

Source: AFTER A LONG HIATUS, ANOTHER SUSPICIOUS BANKER DEATH… (March 2019)

Another individual, who was a very outspoken vaccine whistleblower, and who was a former sales executive for the pharmaceutical company Merck, Brandy Vaughan, was tragically found dead in her home in December of 2020. She made numerous appeals against the push for this highly suspect vaccine, and made videos and posts urging people to investigate her death should she be found dead, especially after she was targeted and stalked for speaking out against the pharmaceutical companies.

Now who would suffer the most if people stayed away from dangerous “medicines” and drugs, and unnecessary vaccines that do more damage than good – and instead learned how to take care of their own immune system and take care of their body through exercise, fresh air and sunlight, a healthy diet and enough sleep?

Hm… maybe… the pharmaceutical/vaccine companies – that Fauci and Bill Gates both have a vested interest in, and who have made multi-millions/billions from various drugs and vaccines.

Covid created 9 new pharma billionaires; combined wealth enough to vaccinate everyone on planet

Hm… and guess who ISN’T liable if these vaccines end up causing severe side effects or even death?…

True.

“Pharmaceutical companies are protected from liability regarding the COVID-19 vaccines. If someone has an allergic reaction or injury from one of the vaccines, they can petition to receive compensation from the Department of Health and Human Services’ (HHS) Countermeasures Injury Compensation Program (CICP).

The National Vaccine Injury Compensation Program (VICP), which also falls under the jurisdiction of HHS, has a better record of providing compensation to people who claim injury from a vaccine than CICP but covers vaccines for diseases such as polio and seasonal influenza, not COVID-19.”

Source: Fact Check: Are Pharmaceutical Companies Immune From COVID-19 Vaccine Lawsuits?

Normally I stay away from anything labeled “fact check”, but this one was scarily accurate. For more information, guess who DOES end up funding vaccine-related injuries?

We, the taxpayers.

“That’s because pandemic-related claims for vaccines will be routed to a rarely used federal program set up to encourage drugmakers to help combat public health emergencies. It spares pharmaceutical and device makers from costly liability lawsuits in exchange for taxpayers compensating injured patients — though it doesn’t guarantee there’s funding to do so.”Drugmakers Shielded from COVID Vaccine Liability But Funds for Injury Claims in Doubt

Lovely, isn’t it? While these multi-billion dollar companies are free from financial liability, it is us, the normal everyday citizens that had no say in the development of these vaccines, to pay compensation to those who end up suffering for these pharmaceutical companies’ malpractice.

Just splendid.

One last note

Is the advent of mind-control technology so far-fetched that it’s nothing more than a “ridiculous conspiracy theory”?

Well, seeing as how DARPA has been aiming at this research for a very long time, and has been actively pursuing it, I’d say if someone still shrugs all of this data and research off, then they have already been mind-controlled.

Genetically tweaking human brains

“To do this, Robinson’s team plans to use viruses modified to deliver genetic material into cells — called viral vectors — to insert DNA into specific neurons that will make them produce two kinds of proteins.”

“The second protein tethers to magnetic nanoparticles, so the neurons can be magnetically stimulated to fire when the headset generates a magnetic field. This could be used to stimulate neurons so as to induce an image or sound in the patient’s mind.”

“The group’s plan relies on specially designed nanoparticles with magnetic cores and piezoelectric outer shells, which means the shells can convert mechanical energy to electrical and vice versa. The particles will be injected or nasally administered, and magnetic fields will guide them to specific neurons.”

Source: The Government Is Serious About Creating Mind-Controlled Weapons (article written “about 2 years ago”)

I’m not liking the sounds of this. (“Mind-Controlled WEAPONS“) Especially if taking it in relation to an article I did last month about possible nanoparticles being injected by the nasal cavity (perhaps by covid swabs?) – Strange Moving White and Black Fibers Found on Masks and Test Swabs

I can’t say exactly what’s going on. But I do know whatever this covid vaccine is, it is NEFARIOUS in purpose, and I just pray that we all get through this and start waking up to these outrageous agendas.

God bless and much love.

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 ParallelVision from Pixabay

Get an Earful

DARPA BRAIN Initiative – Inhumane Experimentations Using Fusion Centers and Electromagnetic Fields to Control & Torture People - "If they want to experiment on you, by the thousands, they will. And you can be driven to insanity and death"
The “FEW” Involved in the “WEF” | Davos and the Purloined Letter Conspiracy. Klaus Schwab’s “Global Leaders of Tomorrow” - "A conspiracy like this could never happen because 'too many people would be involved'." ...
Senator Ron Johnson’s “A Second Opinion” Panel: Renowned Doctors and Medical Experts Discuss Medical Tyranny and Vaccine Injuries/Deaths (Highlight Video – FULL TRANSCRIPT) - Dr. Pierre Kory: "And that’s what I wanted us to be clear that we’re calling attention to today. This is corruption! Plain and simple, it’s corruption!”