Editor’s Note: This is an updated version of our August, 2019 post. It is a sequel to our recent post The Epstein ‘Suicide’: Who was the Real Warden of Metropolitan Correctional Center? A Spook? The […]
Very much appreciated this video by Phil, where he really explains about the 10 days and Darkness. Q did not write “10 days of darkness”, but rather, “Ten days. Darkness.” (see Q post #88). The main part of this begins at about 24 minutes.
I suggest listening at 1.5 – 2x speed, as Phil talks deliberately.
Phil drops enormous pieces of new intel to his followers, and walks through a “hypothetical” “what if” timeline of events.
This was a major “Whoa” moment for me and my mind today.
Through a variety of circumstances and this and that, I connected with someone on the islands (we’ll call them “Basil Fawkes (Falk)”), our discussion led to them mentioning this video, from 2013. I’ve not really paid any attention to Mark Passio, but when I heard this talk, it really connected with my Higher Innards and resonated strongly within me. He talks about the etymology of words we often use, and stresses the need for Inner sovereignty and action.
This is the presentation Mark Passio gave at the Free Your Mind 2 Conference in Philadelphia, PA on April 27, 2013.
In this presentation Mark exposes 10 “New” Age Deceptions, and then offers balanced corrections to each distorted “New” Age “teaching.” If you have fallen for the “feel-good spirituality” of the “New” Age Movement, this presentation will provide a much-needed street-wise viewpoint, and help you to understand how you’ve been deceived by “New” Age Religion.
If you would like to support Janine and Guy with the channel,
here’s a “Buy Us A Coffee” link – https://ko-fi.com/janine12
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All our videos are for entertainment purposes only, just our opinion as we see in the cards-intuitive-psychic interpretation- and not presenting as fact! Enjoy!
This article was previously published October 29, 2021, and has been updated with new information.
Mark Moss, an entrepreneur and financial expert who’s been a full-time investor for over 25 years, is passionate about freedom, liberty and personal wealth. Finances aren’t something I typically focus on, but we’re both in agreement that health is your greatest form of wealth.
I’ll be speaking at Moss’ live event in Miami, Florida, in November 2021, where he and other experts will be sharing how to control your financial future during The Great Reset,1 but in the video above you can hear our recent conversation, which covers everything from key tenets of physical health to how to discern the truth in this era of censorship.
This is only one of three public events I will be speaking at this year. If you want to come and hear me at this event, I arranged with Mark to give you a special discount. Normally these links provide affiliate commissions to me but I asked Mark to give them to you instead to make it more affordable for you to attend. So, if you want a heavily discounted ticket to see me you can click on the link below.
Moss wants to empower people to build wealth, not so they can become greedy or stockpile money, but because money allows you to help other people and have options in your own life. Now, with injection mandates increasing, people are being forced to make a decision to quit their job or put their health at risk from a jab.
“Unfortunately,” Moss said, “we’ve found lots of people who, when the pandemic broke out, didn’t even have $400 saved. When you don’t have that money, when you don’t have those savings, you’re stuck at a dead-end job. If you had money saved, you could quit the job, go look for something else.”
Also, with civil liberties being impacted daily, building wealth gives you the option to change your location to a country or state that may protect your freedom rather than restrict it. He continued:2
“So that’s why we focus on money. It’s not about being greedy, it’s about having options … you’re going to need to have those. The financial system, like the medical system, isn’t really designed for your benefit. It’s designed for the benefit of the people that run the system.
Once you can just start to look at things a little bit differently and, really, it’s a lot more simple than most people make it seem, you can start to build wealth, you can start to then increase your freedom, your options and so forth. Of course, I also look at health as an asset.
You can have all the money in the world, but if you lose your health, you have nothing. I also look at my freedom as an asset. If I have wealth, but I’m locked in my house, that does me no good.”
In order to live your life fully, you really need to have all three: health, freedom and secure finances, which is what the November event is all about.
No. 1 Way to Protect Your Health
Your health is priceless, and many of the most powerful health strategies cost nothing at all or can be implemented very inexpensively. Yet, not only are these natural strategies not taught in conventional medical schools but, if you go against the standard, pharmaceutical-based treatment options you can be challenged, reprimanded or have your license taken away.
This process ostracizing natural therapies began back in 1910 with the release of the Flexner Report, which was written in commission for the Carnegie Foundation.3 The Flexner Report essentially eliminated almost every form of natural medicine, because it was a competitor to the emerging class of pharmaceuticals, primarily derived from oil and petroleum products that Rockefeller was behind.4
It’s similar to the financial system, Moss said, in that your best bet is often to “forget” everything you’ve been taught and open your mind to starting fresh. “I see the same thing in the financial system. Like, you go through economics classes, and then you get a job working for a financial firm, and then you’re just kind of a salesperson, just selling the products they have, and it’s really hard for you to untrain yourself and start looking for those solutions.”5
In relation to your health, it’s important to ignore the mainstream advice to eat vegetable oils, which are more accurately defined as seed oils. Seed oils are hidden in virtually every processed food, including restaurant foods, and there’s virtually nothing more destructive to your body in producing heart disease, cancer, age-related macular degeneration, diabetes, obesity and dementia.6
Chicken and Pork Are a Major Source of Seed Oils
Even if you cut out processed foods and other major seed-oil offenders like sauces and salad dressings at restaurants, you can still be hit by these pernicious toxins because they’re hidden in ostensibly “healthy” foods like chicken and pork. These animals are fed grains loaded with the omega-6 fat linoleic acid, which is found in most seed oils and causes health damage when consumed at the excessive levels that are common today.
Many people eat loads of chicken because it’s perceived as a health food and it’s inexpensive, but it’s a major source of linoleic acid. In your own cooking, examples of healthy fats to use instead of seed oils are beef tallow, butter or coconut oil.
Time-Restricted Eating, Exercise for Better Health
Moss and I also spoke about time-restricted eating, which means condensing your meals into an, ideally, six- to eight-hour window. This will improve your health in a variety of ways, primarily by improving your mitochondrial health and metabolic flexibility. It can also increase autophagy,7 which helps your body clear out damaged cells.
Moss also mentioned nicotinamide adenine dinucleotide (NAD), a vital signaling molecule8 that’s also believed to play an important role in longevity. This is partly due to its role as an essential substrate for sirtuins,9 which are enzymes related to longevity, as well as its role in DNA repair.
NAD modulates energy production and many enzymes and in so doing controls hundreds of processes in your body including the survival of cells and energy metabolism. NAD is influenced on a daily basis by what you eat, exercise levels and more, and also declines with age, leading to changes in metabolism and an increased risk of disease.10
Exercise, especially strength training with blood flow restriction, is one of the best ways to increase NAD levels and energy,11 because it activates NAMPT, an enzyme that’s responsible for NAD biosynthesis.
Another strategy to boost your health and longevity is regular sauna usage. As your body is subjected to reasonable amounts of heat stress, it gradually becomes acclimated to the heat, prompting a number of beneficial changes to occur in your body.
These adaptations include increased plasma volume and blood flow to your heart and muscles (which increase athletic endurance) along with increased muscle mass due to greater levels of heat-shock proteins and growth hormone.12 It’s also a powerful detoxification method, due to the sweating that it promotes.
Unprecedented Manipulation and Censorship
The ability to freely share information such as this is being threatened nearly every day. Due to self-appointed authorities controlling the pandemic narrative, acting as the arbiters of what is right and wrong, and declaring anything against it misinformation, open debate is being stifled and the free sharing of information is censored.
Due to a number of very serious threats against me, personally, and my business, we recently removed 25 years’ worth of content from Mercola.com. This was necessary to persevere in the current censorship climate, as each day rules are being changed to deplatform health advocates. While this threat to freedom is reaching new heights each day, it’s been going on for many years.
Over two years ago, Google took me out of their search engine, and rigged the tool so that, if you look me up, you’ll only see bad information instead of the decades of valuable health information I’ve provided. When you consider that 93% of the world’s online searches use Google,13 you can see that their control runs deep and they — along with other social media platforms — are a major reason why this pandemic brainwashing propaganda campaign has been so successful.
Google has been called a dictator with unprecedented power because it relies on techniques of manipulation that have never existed before in human history, according to Robert Epstein, a Harvard trained psychologist who is now a senior research psychologist for the American Institute of Behavioral Research and Technology, where for the last decade he has helped expose Google’s manipulative and deceptive practices.14
They’re not only a surveillance agency — think about products like Google Wallet, Google Docs, Google Drive and YouTube — but also a censoring agency with the ability to restrict or block access to websites across the internet, thus deciding what you can and cannot see.
Thriving in an Age of Scientific Censorship
“I think the problem used to be getting information,” Moss said. “Today, the problem is maybe too much information. So how do you discern it? And then even now, more importantly, if one side is being erased? So it’s a complex issue, but what can the average person do to, one, be able to discern the information better, and then find the right information?”
Learning how to navigate this unprecedented cancel culture and emerge with the truth is possible, but you’ll typically need to look outside of typical social media platforms. Identify people who you believe are experts in the field and follow what they’re doing.
Many of these experts have had their accounts banned on Facebook, Twitter and even YouTube, so you have to go straight to their site. Using RSS feeds, you can collect information on a variety of topics at once, which makes it a bit easier.
It’s also important to understand that you really cannot trust almost any search engine, even the non-Google search engines, because Google has developed the most effective and sophisticated search engine tool that ever existed, and almost every other alternative search engine uses Google as a search data structure. So, there’s no alternative — it would cost billions, hundreds of billions, to create an alternative.
Then, once you read information, it’s also wise to ask who is benefiting from the information and whether the source is conflicted. It’s so important, Moss says, to “look at the information that you get, get it from trusted sources that you’ve gathered — friends that are like-minded maybe — and just try not to trust everything that you see on Google or YouTube.”15
Building a community of like-minded people is also important, and aligning yourself with those who have healthy habits and who are not brainwashed by propaganda will be a solid strategy going forward.
This is a primary reason for Moss’ live event — to build new connections and provide a strong community support system. It’s now more important than ever that we support each other and work together to sustain resources and develop the creativity to find a solution to the direction the world is headed.
In this interview, Dr. Meryl Nass, an internist specializing in toxicology, vaccine-induced illnesses and Gulf War illness, shares her insights into the dangers of the COVID jab, which received an emergency use authorization October 26, 2021, for children as young as 5.
We also discuss the conflicts of interest within the U.S. Food and Drug Administration that seem to be behind this reckless decision, and how the agency pulled the wool over our eyes with its approval of Pfizer/BioNTech’s Comirnaty COVID injection.
Is the COVID Jab Approved or Not?
As explained by Nass:
“All of the COVID ‘vaccines,’ and most of the COVID treatment products, have not been [FDA] approved. Approved means licensed. All except one, which is the Pfizer vaccine for adults, age 16 and up, which got approved, i.e., licensed on August 23 .
But every other vaccine, and for every other age group, including the boosters, have only been authorized under emergency use authorizations (EUAs). There’s a critical difference [between licensing and EUA]. Once a drug is fully licensed, it is subject to liability.
If the company injures you with that product, you can sue them, unless it later gets put on the CDC’s childhood schedule or is recommended by the CDC [U.S. Centers for Disease Control and Prevention] [during] pregnancy, in which case it obtains a different liability shield.
It then becomes part of the National Vaccine Injury Compensation Program (NVICP, established under the 1986 National Childhood Vaccine Injury Act), and 75 cents from every dose of vaccine that is sold in the United States goes into a fund to pay for injuries that way.”
The National Childhood Vaccine Injury Act removed liability for all vaccines recommended by the CDC for children. Since 2016, they’ve also removed liability for vaccines given to pregnant women, a category that has become the latest “gold rush” for vaccines. Naturally, once a company is no longer liable for injuries, the profitability of the product in question increases dramatically.
Countermeasures Injury Compensation Program Is Nearly Useless
Products under emergency use have their own special government program for liability called the Countermeasures Injury Compensation Program (CICP). “It is a terrible program,” Nass says. CICP is an offshoot of the 2005 PREP Act.
“The PREP act enabled the CICP to be created by Congress,” Nass explains. “Congress has to allocate money for it. If you are injured by an emergency use product, you don’t get any legal process. The companies have had all their liability waived. There is a single process that is administered through HHS [Health and Human Services].
Some employees there decide whether you deserve to be compensated or not. The maximum in damages you can obtain is about $370,000 if you’re totally disabled or die, and the money is only to compensate you for lost wages or unpaid medical bills.”
So far, even though several hundred CICP claims have been filed for injuries resulting from the COVID shots, not a single claim has been paid out. This is important, because the statute of limitations is one year. “It’s getting close to running out for people who were vaccinated early,” Nass says.
If you fail to apply in time, you lose the opportunity to get any compensation entirely. “Of course, in fact, it’s really ‘an opportunity’ to apply and get nothing because almost nobody gets paid,” she says. At that point, you have no further recourse. There’s no appeals process to the judicial system.
“You can ask the HHS twice to compensate you, and if they say no, that’s it,” Nass explains. “You can attempt to sue the company that made the product, if you’re convinced it was improperly made, but the secretary of HHS has to give you the permission to sue.
You have to prove that there was willful misconduct and no one has ever reached that bar. So, there has never been a lawsuit under this. Anyway, that’s what you’re looking at. If you get the vaccine under EUA and are injured, you’re on your own. People have no idea about this when they vaccinate themselves or their children.”
Why Were the Shots Mandated?
As you know by now, president Biden decided to mandate the COVID jab for most federal employees (but not all) and private companies with 100 employees or more. “We don’t know why that is,” Nass says. It doesn’t make sense, as large numbers of Americans have already recovered from COVID-19 and have durable, long-lasting immunity already.
As correctly noted by Nass, natural immunity is much stronger than what you can achieve from the injection, which only provides antibodies against the SARS-CoV-2 spike protein and wears off within a few months. The shots “may in fact permanently limit the kind of immune response you would make were you to be infected with COVID later,” Nass says.
For these reasons, there’s absolutely no good reason to vaccinate people who have recovered from the infection and several bad reasons. There’s evidence showing the shot can be more harmful for those with existing immunity.
“But for reasons best known to itself, the Biden administration feels so certain it needs to vaccinate everybody that it has used illegal means to tell employers they will lose federal contracts if they don’t force their employees to be vaccinated immediately, and must fire them — if they’re health care workers, for example, or government employees, or military — if they have not been vaccinated.
Obviously that is creating a great deal of chaos, particularly within the health care industry, particularly in my state, Maine, where these draconian rules have gone into effect and many fire department, police, EMTs, nurses and doctors can no longer work.
The one thing that was necessary to push mandates forward was for the government to be able to say it had a licensed product. Before the emergency use authorization was created in 2005, you had licensed drugs and you had experimental drugs and nothing else.
There was no gray area between them. Any use of a medication or vaccine that is not fully licensed is still experimental, despite the fact that a new category of drugs has been created with emergency use authorizations.
These are still experimental drugs, so under emergency use, you can’t force people [to take them]. You have to offer them options and they have the right to refuse. Since that is part of the statute, the federal government can’t get around it.
Therefore, attorneys in the Biden administration knew they could not legally impose mandates under an EUA, and so they demanded that FDA provide a COVID vaccine full approval, aka, an unrestricted license. This was believed to enable them to impose mandates.
They must have put pressure on the FDA, and FDA gave them what they wanted, which was a license for the Pfizer vaccine called Comirnaty on August 23 .”
Comirnaty Approval Includes Important Caveats
In the documents released August 23, 2021, by the FDA, there were some interesting caveats. They said the Comirnaty vaccine is essentially equivalent to the EUA vaccine and the two vaccines may be used interchangeably. However, they pointed out that the two are legally distinct. Curiously, FDA didn’t specify what these legal distinctions are.
“I concluded that the legal distinctions were the fact that under EUA, there was essentially no manufacturer liability, but once the vaccine got licensed, the manufacturer would be subject to liability claims unless and until the vaccine was placed on the childhood schedule or recommended in pregnancy, in which case it would then fall … under the NVICP,” Nass says.
“Right now, Comirnaty is still not in that injury compensation program, and it’s licensed, so it no longer falls under the CICP. So, it is in fact subject to liability if you get injured with a bottle that says Comirnaty on it. Of course, if you’re Pfizer, what do you want to do?
You don’t want to make that licensed product available until several months have gone by and Comirnaty has been put into the National Vaccine Injury Compensation Program. So, Pfizer and FDA have not made the licensed product available yet.
What has happened instead, in the military, is the FDA has made a secret deal with the military and said, certain emergency use lots can be considered equivalent to the licensed vaccine, and [told military medical staff] which QR codes — which lots can be used. [These specific lots] can then be given to soldiers as if they’re licensed.
Subsequently, we’re told that military clinics are actually putting Comirnaty labels onto bottles that are under EUA. Now, that probably can happen in the military, but only in the military, because there are likely to be memoranda of understanding within the military that we haven’t seen yet that say soldiers cannot sue Pfizer for injuries …
In the military, the government and Pfizer feel like they have set up a situation where nobody can sue, but in the civilian world, that has not happened, and so there is no Comirnaty available.
Yet, on the basis that FDA licensed this product, the federal government is still telling employers that they can mandate it and that they must fire employees that have not taken the vaccine, or they will lose government contracts. We’re in a very interesting situation that is ripe for litigation, and Children’s Health Defense, which is an organization I represent, is litigating some of this.
However, the litigation situation has been very difficult since the pandemic began. Cases that normally would’ve been easy wins are being thrown out by the courts, both in the U.S. and in Europe. Something strange has happened and the judges are looking for any way out, so they don’t have to rule on the merits of these cases.”
The organization Children’s Health Defense has filed a lawsuit arguing you cannot have a vaccine that is both an emergency use product and a licensed product at the same time. That’s against the law, but the federal government did it anyway. Remarkably, the request for an injunction was initially thrown out, but Children’s Health Defense hasn’t given up and is still pursuing that case.
COVID Jab Is Authorized for 5- to 11-Year-Olds in the US
As mentioned, the FDA recently authorized the EUA COVID jab for children between the ages of 5 and 11, which is simply appalling, considering they are at virtually no risk from COVID-19. I’ve not seen a single recorded case in the entire world of anyone in that age group dying of COVID that didn’t have a serious preexisting comorbidity, such as cancer.
If you have a healthy child, they are at no risk from the infection, so there’s only danger associated with this shot, which in this age group would be one-third the adult dose. Typically, when you’re giving a drug to a child, the dose is calculated based on the child’s weight. Here, they’re giving the same dose to a 5-year-old as an 11-year-old, despite there being a significant difference in weight. So, it’s pure guesswork.
Worse yet, the mRNA vaccines produce an unpredictable amount of spike protein, and even if they produce much too much, there is no way to turn off the process once you have been injected.
Despite clear safety signals, the FDA’s advisory committee authorized the Pfizer jab for 5- to 11-year-olds unanimously, 17-to-0 (with one abstaining vote). However, when you look at the roster of the FDA’s committee members1 who reviewed and voted to authorize the Pfizer shot for children as young as 5, the unanimous “yes” vote becomes less of a mystery.
Abhorrent Conflicts of Interest
As reported by National File2 and The Defender,3 the membership of the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) has had staggering conflicts of interest. Members have included:
A former vice president of Pfizer Vaccines
A paid Pfizer consultant
A recent Pfizer research grant recipient
A mentor to Raphael Simon, senior director of vaccine research and development at Pfizer
James Hidreth — President of Meharry Medical College, which administers Pfizer vaccines
A chair of the Independent Data Monitoring Committee for the Pfizer Group B Streptococcus Vaccine Program
An individual proudly photographed taking a Pfizer vaccine
Several people who are already on the record supporting coronavirus vaccines for children, including Ofer Levy, Jay Portnoy and Melinda Wharton
In addition to that, former FDA commissioner Scott Gottlieb is currently on Pfizer’s board of directors. As noted by Nass, two of the members, one permanent and one temporary, are also CDC career employees whose job it is to push vaccines at the CDC.
“If they voted against authorizing a vaccine, they would be out of a job,” Nass says. “They have no business on that committee … It’s a very unethical stew of advisory committee members …
What happened is Pfizer delivered a large package of information to the FDA on October 6, 2021. FDA staff had to go through this large packet of information on the 5- to 11-year-olds and produce their own report, which was about 40 pages long, and create talks to give to the advisory committee, and they did all of this in 17 days.
There was apparently very little critical thought that went into their presentations. Before the meeting, Children’s Health Defense, and I was one of the authors, wrote to the committee and to FDA officials saying, ‘Look, there’s all these reasons that don’t make logical or medical sense for vaccinating kids in this age group, because they almost never get very ill or die, and the side effects of the vaccine are essentially unknown.
We know there are a lot of side effects, but the federal government has concealed from us the rate at which these side effects occur. But we know that the rate from myocarditis is very high, probably at least 1 in 5,000 young males … which is a very serious side effect. It can lead, probably always leads, to some scarring. It can lead to sudden death, to heart failure.”
Trials in Young Children Were Insufficient
As explained by Nass, in the clinical trial, there were two groups of children. The first group was enrolled for two to three months, while the second group was enrolled for just 17 days after receiving the second dose. (Pfizer added the second group because FDA claimed there weren’t enough volunteers in the first group.)
These two groups comprised over 3,000 children who got the jab and 1,500 or 2,000 who got a placebo. None suffered serious side effects. This was then translated into the claim that the injection was safe. However, as noted by Nass:
“They didn’t look at safety in all these kids. Even though FDA had said, ‘Add kids to your clinical trial,’ Pfizer created a ‘safety subset’ of one-tenth of the vaccinated subjects.
It was this small number of kids from whom they drew blood to show they had adequate levels of neutralizing antibodies, which was a surrogate for efficacy, because they didn’t have enough cases of COVID in this abbreviated trial to show that the vaccine actually works in this age group.”
Even though the advisory committee acknowledged that the blood test done for efficacy had not been validated, and wasn’t reliable evidence of effectiveness, they still decided that all children, regardless of health status, would benefit from the injection.
They also ignored the fact that at least half the children are already immune, and giving them the injection will provide no additional benefit in terms of immunity, while putting them at increased risk for serious side effects.
“Nobody said, ‘Look, the parents of healthy kids may be dying for a vaccine, but that’s because we haven’t told them the truth about the vaccine. We haven’t told them their kids don’t need it. We haven’t told them it’s going to potentially damage future immunity.
We haven’t told them they’re at higher risk of side effects than if they never had COVID. We’re not allowing them to go get antibody tests to establish that they’re already immune and therefore should be waved from being vaccinated.’
The committee members were aware of all this stuff, but in the end [they voted yes] … apart from one very smart member of the committee who works for the National Institutes of Health. He abstained. He didn’t have the guts to vote no, but he knew this was a bad idea.”
Children Are Being Injected Without Parental Consent
While all of that is bad enough, parents of young children now face the possibility of their children being injected against their will and without their knowledge. Nass comments:
“As I said, we don’t know why the government wants everybody vaccinated, but there’s probably a reason that goes beyond protecting us from COVID.
The government got the FDA to authorize the vaccine for 12- to 15-year-olds on May 10 , and subsequently that group, which is about 6 million kids, has been getting vaccinated across the country. That’s under emergency use so, again, you can’t sue.
But something kind of evil happened, which was many cities began vaccinating 12- to 15-year-olds in the absence of parental permission. So, a child could show up with their friends or a friend’s mother at a vaccine center and get vaccinated with no one asking about their medical history, nobody calling the parents. No notation got entered into the child’s medical record that they were vaccinated.
Vaccinators were told to make their own assessment. If they thought this child could give consent, go ahead and vaccinate. Now, that is a gross violation of our laws, and yet it was happening in Boston, in Philadelphia, in Seattle, in San Francisco, and we have good documentation of it.
The government currently is planning for mobile vaccination clinics for kids and vaccinations in schools, and they may take this program of vaccinating without parental consent down to the 5- to 11-year-olds …
In fact, we may see clinics popping up that don’t require informed consent in the 5- to 11-year-old group. Let me just mention that the chief medical officer in Canada’s British Columbia said they have brought laws that allow children of any age to consent for themselves. Think about that. A baby can consent for vaccinations for itself. It would be funny if it wasn’t so diabolical.”
All of this goes against the most basic concept of medical ethics, which is informed consent. No one has the right to perform a medical procedure on you without your consent, or the consent of a legal guardian. The government, again, without establishing any new laws, is simply bypassing the legal system.
Will Young Children Be at Risk for Myocarditis?
Based on her review of the scientific literature, Nass suspects younger children in the now COVID jab-approved, 5- to 11-year-old age group will be at exponentially higher risk of myocarditis and other side effects compared to the 12- to 15-year group, where we’ve already seen a documented increase.
“In the letter that Children’s Health Defense wrote to the advisory committee for the FDA, we created a graph based on the reporting rate of myocarditis versus age, and we showed there was an exponential curve.
Men aged 65 and up had a rate that was 1/100th the rate of boys aged 12 to 17. If that exponential curve keeps going up, the rate in the 5- to 11-year-olds could be even dramatically higher. In those young men, a 1 in 5,000 rate was reported to VAERS [Vaccine Adverse Events Reporting System]. That’s not a real rate.
That just tells us how many people got diagnosed with myocarditis, and then went to the trouble of reporting it to the FDA. The FDA and CDC have a large number of other databases from which they can gather rates of illness.
VAERS is considered passive reporting. It is not considered fit for purpose to establish illness rates because we don’t know how many people report. Do 1 in 10 report, 1 in 100, 1 in 50? Nobody knows.
However, again, because everything is crazy since the pandemic came in, the CDC has tried to pull the wool over our eyes and has claimed that the rate of anaphylaxis in the population from COVID vaccines is identical to their reporting rate to VAERS. We know that’s not true.
On the CDC’s website, that’s what they have. Elsewhere on the website, they say you can’t take a VAERS rate and call it an actual rate of reactions, but they’ve done that [for anaphylaxis]. And they’re trying to obfuscate the fact that they’re not giving you real rates, and sort of pretending that the myocarditis rate is probably the VAERS reporting rate of myocarditis, although they’re not saying so directly.”
Nass goes on to recount an example from the smallpox vaccine, which also caused myocarditis. A military study that just looked at cases sent to specialists found roughly 1 in 15,000 developed myocarditis. A military immunologist then dug deeper, and drew blood on soldiers before and after vaccination, and found a myocarditis rate of 1 in 220 after receiving the smallpox vaccine.
However, 1 soldier in 30 developed subclinical myocarditis where troponin rose from normal to more than two times the upper limits of normal. While asymptomatic, 1 in 30 had measurable inflammation of the heart. “Right now, in terms of what the rate is for COVID, nobody is looking, no federal agency wants to find out the real rate,” Nass says.
You Can’t Find Problems You Refuse to Look For
A simple study that measures troponin levels — a marker for heart inflammation and damage — before and after each dose, could easily determine what the real rate of myocarditis is, yet that is not being done.
“This is what we’re dealing with,” Nass says. “All these databases, which is about a dozen different databases, that CDC and FDA said they could access to determine the rates of side effects after vaccination with COVID vaccines, they’re either not being used or being used improperly,” Nass says.
“It was discovered that a new algorithm was being used to study the VAERS database that only came into use in January 2021, immediately after the vaccines were authorized, and the algorithm was developed such that you compare two vaccines to each other.
If the pattern of side effects was similar between the two vaccines — which is often the case because there’s a limited number of general vaccine adverse reactions — even if one vaccine has a thousand times more side effects as the one it is being compared to, by using this flawed algorithm, if the pattern of reactions was the same, even though the rates were 1,000 times higher for one, the algorithm would fail to detect a problem.
That is the algorithm they’re using to analyze VAERS [data]. They’re also using bad methods … to analyze the vaccine safety database, which encompasses 12 million Americans who enrolled in HMOs around the country. The CDC pays for access to their electronic medical records and their data.
Somehow when these databases have been looked at carefully, they’re finding very low rates of myocarditis in boys, approximately equal to the VAERS reporting. It was said months ago, ‘We can’t find a safety signal for myocarditis. We’re not finding an anaphylaxis signal. we’re not finding a Bell’s palsy signal.’
The FDA’s and CDC’s algorithms couldn’t pick up for most known side effects. So, there’s something wrong with the analytic methods that are being used, but the agencies haven’t told us precisely what they are. What we do know is that the rates of side effects that are being reported to VAERS are phenomenal.
They’re orders of magnitude higher than for any previous vaccines used in the United States. An order of magnitude is 10-fold, so rates of reported adverse reactions are 10 to 100 times higher than what has been reported for any other vaccine. Reported deaths after COVID in the United States are 17,000+. It’s off the charts.
Other side effects reported after COVID vaccinations total over 800,000. Again, more deaths and more side effects than have ever been reported for every vaccine combined in use in the U.S. cumulatively over 30 years.”
Despite all this shocking data, our federal agencies look the other way, pretending as if nothing is happening, and no matter how many people approach them — with lawsuits, with public comments, reaching out to politicians — they refuse to address blatantly obvious concerns. This is clear evidence that they’re acting with intentional malice.
The FDA and CDC are supposed to protect the public. They’re supposed to identify safety concerns. They’re not supposed to act as marketing firms for drug companies, but that’s precisely what they’ve been converted to.
New Formulations Have Never Been Tested
Another truly egregious fact is that Pfizer has altered its formulation, allegedly to make it more stable, but this new formulation has never been included in any of the trials. Nass explains:
“During the October 26, 2021, VRBPAC [Vaccines and Related Biological Products Advisory Committee] meeting, Pfizer said, ‘Look, we want to give the vaccines in doctor’s offices and we’ve found a way to stabilize the vaccine so we don’t need those ultra-cold fridges anymore. We can put these vials in a doctor’s office and, once defrosted, they can sit in a regular fridge 10 weeks and they’ll be fine.’
Some committee members asked, ‘OK, what’d you do? How did you make this marvelous discovery?’ And they said, ‘We went from the phosphate buffered saline buffer to a Tris buffer, and we slightly changed some electrolytes.’ A committee member asked, ‘OK, how did that make it so much more stable?’ And everybody in the meeting from FDA and Pfizer looked at each other and said, ‘We don’t know.’
An hour later, Pfizer had one of their chemists get on the line, but he couldn’t explain how the change in buffer led to a huge increase in stability, either. Then, later in the meeting, one of the members of the committee asked, ‘Did you use this new formulation in the clinical trial?’
And Dr. Bill Gruber, the lead Pfizer representative, said, ‘No, we didn’t.’ In other words, Pfizer plans, with FDA connivance, to use an entirely new vaccine formulation in children, after their clinical trials used the old formulation. This is grossly illegal. They’ve got a new formulation of vaccine. It wasn’t tested in humans. And they’re about to use it on 28 million American kids.”
It’s nothing short of a dystopian nightmare. Completely surreal. You can’t make this stuff up. Yet as shocking as all this is, earlier this year, Dr. Anthony Fauci projected that these COVID jabs would be available for everyone, from infants to the elderly. Now they’ve got the 5-year-olds, and there’s every reason to suspect they’ll go after newborns and infants next.
Whose Babies Will Be Offered Up as Sacrificial Lambs?
According to Nass, Pfizer and the FDA have struck a deal that will allow Pfizer to test on babies even younger than 6 months old, even if there’s no intention to inject infants that young. Those trials may begin as early as the end of January 2022.
“This arrangement between FDA and Pfizer will give Pfizer its extra six months of patent protection, whether or not these vaccines are intended to be used in those age groups. So, you can look at these trials as a way of almost sacrificing little children, because when you start a trial, you don’t know what the dangers are going to be.
I could be wrong, but I doubt we’re going to give these to newborn babies the way we give the hepatitis B vaccine on the date of birth, yet they will be tested in very young babies. The question is, whose babies get tested? In the past, sometimes the babies that got tested were foster children, wards of the state. Sometimes parents offer up their children. But there will be clinical trials.”
When will we get the data from those trials? It turns out that in the agreements reached between Pfizer and the FDA, some of those trials won’t conclude until 2024, 2025 and 2027. The goal here is to vaccinate all Americans, children and adults, within the coming few months or a year, yet it’ll be five years before we actually know from clinical trials what the side effects may be.
We’re Living in Clown World
As noted by Nass, this is yet another crime. It may fulfill the letter of the law, but it doesn’t fulfill the meaning of the law. It makes no sense to run clinical trials that won’t be completed until five years after your mass vaccination program has been completed and the entire population is injected.
“It’s just a joke to do that,” Nass says. “But FDA has become Clown World, and what they do now is to perform a charade of all the normal regulatory processes that they are expected to do, but they’re only doing them in an abbreviated or peculiar manner so that they don’t really collect the important data.
For example, the control group has been vaccinated two months into the Pfizer trials, which effectively obscures side effects that develop after two months. Blood is not tested for evidence of myocarditis or blood clots using simple tests (troponin and D-dimer levels).
For all the Americans out there who haven’t spent 20 years examining the FDA procedures like I have, these FDA advisory committee meetings are it’s designed to make you think a real regulatory process is going on, when it’s not. Instead we are all guinea pigs, but no one is collecting the data that would normally be required to authorize or approve a vaccine. Therefore, in my opinion, nobody should get these shots.“
To make matters even worse, it’s actually illegal to grant EUAs for these vaccines, because there are drugs that can prevent the condition (COVID), as well as treat it. EUAs can only be granted if there are no existing approved, available alternatives to prevent or treat the infection.
The effective drugs most have already heard of are ivermectin and hydroxychloroquine, but there are a number of other drugs that also have profound effects on COVID, Nass says, including TriCor and cyproheptadine (Periactin).
TriCor, or fenofibrate, emulsifies lipid nanoparticles and fatty conglomerations that contain viruses and inflammatory substances. The drug essentially allows your body to break down the viral and inflammatory debris better. As such, it might also help combat complications caused by the nanoliposomes in the COVID shot.
According to Nass, Pepcid at high doses of up to 80 milligrams three times a day is also useful for treatment. Dr. Robert Malone is starting a clinical trial using a combination of Pepcid and celecoxib (brand name Celebrex). Many are also recommending aspirin to prevent platelet activation and clotting.
I believe a far better alternative to aspirin is lumbrokinase, and/or serapeptase. Both are fibrinolytic enzymes that address blood clotting. You can develop sensitivity to them, so I recommend alternating the two on alternate days for about three months if you’ve had COVID.
You could rule out blood clotting by doing a D-dimer test. If your D-dimer is normal, you don’t need an anticlotting agent. If clotting is a concern, you could also use NAC in addition to these fibrinolytic enzymes. It too helps break up clots and prevent clot formation.
“Remember, all the COVID jabs are authorized [under EUA], not licensed. They’re all legally, technically, experimental. I know you can lose your job and all these terrible things can happen if you refuse the vaccine, but if you are injured by the shot, you won’t be able to sue later. You will be on your own.
Legally, they can’t force you to accept the vaccine while it is in EUA status because of the Nuremberg code, because of existing U.S. law about informed consent, and because of the actual statute on emergency use authorization, which says you have the right to refuse. They can’t force you to take these [shots].
I know they are forcing you, but legally they can’t, and please keep that in mind. Hopefully these wrongs will be redressed. Mandates are being walked back in many jurisdictions.
As I’ve told people, demand to see the bottle that says Comirnaty, because legally, they can force the licensed product on you, but there isn’t any right now. So, you have an out for the next few months, hopefully.
They’re really dangerous vaccines. What you don’t know will hurt you. Please protect your children. If there’s any way, don’t get vaccinated. The more people who say no, the more the government is already backing down. In many cities, the imposed dates by which you have to be vaccinated have been pushed back.
Now Biden’s administration is saying, ‘Well, it’s not going to be carved in stone. We’re going to negotiate with people because they don’t want to lose 30% or 40% of their staff.’ So, be strong, protect yourself and your children. Know you’re doing the right thing.
We’ve got a criminal organization running things now. This is a worldwide program of some kind designed to control us. Once we all figure it out, we can win. There’s many, many more of us than there are of them.”
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