The 5G Roll Out: EMF Radiation, Devastating Health Impacts, Social and Economic Implications. Crimes Against Humanity?

What are the real effects of 5G radiation? & “Why is 5G Important for the Fourth Industrial Revolution?”

This article has been cross-posted from globalresearch.ca

Original article written by Richard Gale and Dr. Gary Null
on January 20, 2022

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The roll out of the new C-Band 5G service by AT&T and Verizon scheduled for January 19, has raised alarms for major airline executives who have warned that it will create “catastrophic” interference with flight navigation systems and pilot safety during take off and landing.  The risks will be greater during bad weather. Among the warnings are major disruptions in commerce and supply chain, the overriding of aircrafts’ electronic safety systems and radio altimeters, and the grounding of flights that will leave “tens of thousands of Americans grounded.”

According to CNN, the airlines estimate that upwards to 1,000 flights will be disrupted daily. The 5G threat is particularly heightened in low-visibility conditions. Chief executives from American Airlines, United, Delta, Southwest and Jet Blue have demanded that 5G be blocked within a two-mile radius of major US airports. FedEx and UPS have also joined the airlines’ complaints. Foreign airlines such as Dubai’s Emirates, Air India, Japan Air, Lufthansa and British Airways have already changed or canceled flights to the US. Two of the world’s largest plane manufacturers, Airbus and Boeing, have also issued warnings.

This has become an ongoing battle between the Federal Aviation Administration and the private telecomm industry and its Washington lobbyists. The FAA has been warning about 5G interruption of planes’ navigation systems for quite some time.  The telecomm industry’s unwillingness to budge is most disturbing because the Biden administration has already permitted 90 percent of wireless tower deployment to roll out as scheduled.  It is only in the vicinity of major airports where the FAA and airlines demand restrictions due to safety concerns. However, as we have reported for the past several years, the telecomm giants, notably AT&T and Verizon, and its leading media spokespersons at CNN and the New York Times, have undermined and denied 5G’s risks, especially to human health and the environment, ever since wireless technologies were first commercialized.

5G is destined to be a permanent fixture across the nation. There is barely a chance to prevent it. The thousands of medical and environmental studies confirming high EMF’s dangers and the petitions signed by thousands of international scientists to halt its deployment are unequivocally ignored or worse ostracized and canceled.

It is estimated that there are over 10,000 peer-reviewed clinical studies mentioning serious molecular biological injury and defects to organs, neurons, cells and cellular function, and DNA damage to plants, animals and humans alike.  Between August 2016 and September 2018 alone, over 400 new studies on electromagnetic radiation risks were compiled by public health Professor Joel Moskowitz at the University of California at Berkeley.

Despite the pandemic, lockdowns and social distancing have not hindered 5G’s progress to connect every American into its spider’s web.  In December 2019, T-Mobile reached its goal of nationwide 5G coverage of over 1.3 million square miles (34 percent of the US) and AT&T reached its milestone to reach 179 million people. The 5G roll out is also crucial for international globalists to usher in the Fourth Industrial Revolution.

The World Economic Forum’s presentation, “Why is 5G Important for the Fourth Industrial Revolution,” outlines the multi-trillion dollar impact advanced connectivity will have on manufacturing, wholesale and resale, smart cities and homes, public services, transportation, real time banking, finance and insurance, agriculture and forestry, micro chip surveillance, real estate, education, mining, health and medicine.

We must not hold any false hopes that the Biden administration will ultimately side with the airlines’ safety concerns. During the 2020 election, the Biden campaign received $97 million from the Communications/Tech sector versus Trump’s $18 million.  Alphabet (Google), Microsoft, Amazon, Facebook, Apple, AT&T and Comcast overwhelmingly contributed to Biden’s war chest.

The American public is being bamboozled with blatant falsehoods to embrace 5G as a necessary and innovative technology that will benefit and improve our lives. But the real truth is the exact opposite.

The following information has been abbreviated from scientific literature that is fully validated and has been stated by international experts such as Drs. Devra Davis and Martin Pall about EMF’s adverse effects to government leaders and national legislators repeatedly. This outline was presented by Dr. Martin Pall, a Professor Emeritus of Biochemistry and Medical Sciences at Washington State University to the National Institutes of Health. Dr. Pall is recognized worldwide as an expert in EMF and 5G’s detrimental effects on biological systems and the diseases associated with wireless technologies.

  • Lower Fertility: Alters the structure of the testes and ovaries, lowers sperm count and the number of egg follicles, increases spontaneous abortion and lowers the levels of three sex hormones.
  • Neurological and Neuropsychiatric Effects: There has been a dramatic increase in the following conditions since the advent of mobile phones, the internet, and wireless technologies:  insomnia, fatigue, depression, headaches and cognitive dysfunction, anxiety, and loss of memory. Animal studies have shown that EMFs produce major changes in brain structure, which is likely happening to everyone who has extensive daily exposure to EMFs
  • Cellular DNA Damage: There are three types of DNA damage observed in EMF exposure:  single and double DNA breaks and oxidized DNA bases.  These can cause cancer and mutations in the sexual germ lines.
  • Apoptosis: EMFs contribute to programmed cell death that in turn leads to reproductive and neurodegenerative disorders.
  • Oxidative Stress: Free radical damage that has been associated with numerous health conditions including cancer, diabetes, rheumatoid arthritis, myocardial infarction, stroke, chronic inflammation, Parkinson’s, multiple sclerosis, cellular death and aging
  • Endocrine Effects: According Dr. Pall, every hormonal system in the body is adversely affected by EMF exposure.
  • Excessive Intracellular Calcium: Ca2+ is critical for cellular activity
  • Cancer: There are 35 separate scientific reviews of the body of peer-reviewed literature providing evidence that EMFs increase carcinogenesis, promote and progress tumor development and contribute to metastasis.

There are also other medical conditions that have been shown to be associated likely with EMF exposure:

  • Cardiac Effects. EMFs interfere with the electrical control of the heart that can produce tachycardia, bradycadia, arrhythmia and abnormal heart palpitations.
  • Early Onset of Alzheimer’s and Dementia: In recent years and in parallel with increased EMF exposure, signs of symptoms associated with Alzheimer’s are being observed in people age 30 and younger. Dr. Pall has called this “digital dementias.”
  • ADHD and Autism: The epidemic in ADHD and autism witnessed in each younger generation may be caused by late prenatal and early post-natal EMF exposure. Each of these neurological conditions is associated with the increase of calcium over-penetrating cell linings due to EMF pulsations and disrupting synapse formations.

Everyone will be affected by 5G’s radiation. But it will not require three decades to observe its injurious effects. Unlike cigarettes, nobody has a choice whether you wish to be exposed to 5G or not. 5G’s EMF radiation is all-pervasive.

The mainstream media, in particular the New York Times, which has a collaborative agreement with the leading 5G provider Verizon, have no intention to warn the public about any of the scientific findings mentioned above. There is a growing consensus in the scientific and medical community that 5G will usher an epidemic of disease never before witnessed in human history. It is too difficult to make forecasts. Nevertheless, if the past and current research on EMF’s adverse effects on health and the environment during the past 50 years are any indication, we are entering a new epoch of disease and neurological disorders that humanity is completely unprepared to handle.

This is a consequence of what happens when an entire nation is trapped into carelessly trusting elected presidents and legislators whose campaigns are bankrolled by the Telecomm giants and Silicon Valley, and a media empire ruled by serial liars and masters of disinformation campaigns for private corporate interests. This is vulture capitalism at is worse.

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Richard Gale is the Executive Producer of the Progressive Radio Network and a former Senior Research Analyst in the biotechnology and genomic industries.

Dr. Gary Null is host of the nation’s longest running public radio program on alternative and nutritional health and a multi-award-winning documentary film director, including his recent Last Call to Tomorrow

They are regular contributors to Global Research.

*Featured image credited to globalresearch.ca

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.

Prominent US Hospitals Drop Vax Mandates after Massive Shortage of Key Staff

“thousands of nurses have left the industry or lost their jobs rather than get vaccinated” for COVID-19.

This article has been cross-posted from globalresearch.ca
Original article written by Ashley Sadler / LifeSiteNews (December 13, 2021)

All Global Research articles can be read in 51 languages by activating the “Translate Website” drop down menu on the top banner of our home page (Desktop version).

To receive Global Research’s Daily Newsletter (selected articles), click here.

Visit and follow us on Instagram at @crg_globalresearch.

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Major hospital systems have had to reevaluate their coercive COVID-19 jab policies after crucial employees, especially nurses, have opted to quit rather than get the experimental injections.

Facing serious staffing shortages, some of the largest and most prominent hospital systems in the United States, including HCA Healthcare Inc., Tenet Healthcare Corp., AdventHealth, and Cleveland Clinic have been forced to backpedal on their COVID-19 jab mandates in hopes of retaining crucial employees, The Wall Street Journal reported Monday

Townhall reported that University Hospitals in the Cleveland, Ohio area also recently announced the reversal of its jab mandate for hospital workers.

According to The Wall Street Journal, the major hospital systems have been forced to reevaluate their coercive COVID-19 jab policies after needed healthcare industry employees, especially nurses, chose to quit rather than get the experimental injections.

 

“Vaccine mandates have been a factor constraining the supply of healthcare workers, according to hospital executives, public-health authorities and nursing groups,” the report noted, adding that “thousands of nurses have left the industry or lost their jobs rather than get vaccinated” for COVID-19.

The Journal cited the Centers for Disease Control and Prevention (CDC) in reporting that as of September, unvaccinated employees accounted for a massive 30% of workers employed by over 2,000 U.S. hospitals.

Many people, including healthcare professionals, have been skeptical of the push toward mass immunization. The CDC reports an infection survival rate of greater than 99.95% for those under age 50. Meanwhile, the list of FDA-recognized adverse events has grown from severe anaphylactic reactions to include fatal thrombotic events, the inflammatory heart condition myocarditis, and neurologically disabling disease like Guillain Barré Syndrome, as well as thousands of recorded deaths and permanent disabilities.

The staggering percentage of healthcare workers who have refused to comply with the jab requirements imposed by their hospital systems — many of whom are vitally necessary nursing personnel — could have a crippling effect on America’s hospitals if the establishments move to fire all noncompliant workers.

Recognizing this dilemma, an employee-benefits lawyer has suggested that hospitals that don’t mandate the jabs could see an influx of interested applicants fleeing hospitals with more coercive policies.

“It’s been a mass exodus, and a lot of people in the healthcare industry are willing to go and shop around,” Wade Symons, head of the consulting firm Mercer’s U.S. regulatory practice, told the Journal.

News of the major hospital systems dropping their injection mandates comes after a federal judge in Louisiana blocked the Biden administration’s top-down federal COVID-19 jab mandate for healthcare workers that would have impacted at least 10 million Americans.

The judge’s late-November decision was in response to President Joe Biden’s September 9 announcement of a series of vaccine mandates for public and private sectors, including one with no testing option for millions of healthcare workers employed by medical facilities that receive Medicare and Medicaid funding.

 

The Centers for Medicare & Medicaid Services (CMS) has subsequently announced it will temporarily halt enforcement of its healthcare worker mandate pending appeal of a federal injunction blocking the measure.

“I don’t think the mandates were helpful and I think the court in Louisiana did everyone a service,” Alan Levine, chief executive officer of Ballad Health, told The Journal. 

Levine, who told the newspaper his company employs about 14,000 people, of whom roughly 2,000 have opted not to get the shot, said firing “[t]hat many people … would have been devastating to our system.”

Before the Louisiana judge blocked the mandate, at least 22 states had joined a duo of joint lawsuits against the Biden administration over the rule.

States, companies, and private individuals have filed a raft of lawsuits taking issue not only with the mandate for healthcare workers but also the mandate for federal contractors and another for businesses with 100 or more employees.

In early November, a federal court blocked the mandate for large businesses, just two days after it was published. The mandate would have used the Occupational Safety and Health Administration (OSHA) to impose massive fines on noncompliant companies and individuals for failing to get the experimental shots.

By early December, all three of the Biden administration’s private sector jab mandates were stalled by federal judges.

 

The latest mandate to be blocked was halted December 7 by a federal judge who sided with South Carolina’s attorney general and Republican governor and stopped the Biden administration’s COVID-19 jab mandate for federal contractors, freezing the requirement nationwide and marking the third federal injection mandate to be blocked across all 50 states.

A shift in public policy toward the reversal of coercive jab mandates comes as many Americans remain concerned that the experimental drugs on the market have not been sufficiently studied for negative effects given their accelerated clinical trials. Many also harbor serious moral reservations about the use of cells from aborted babies in the development of the shots.

Still others simply consider the injections unnecessary given COVID-19’s high survivability among most groups, low risk of asymptomatic spread, and research indicating that post-infection natural immunity is either just as protective against reinfection or provides even greater protection.

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