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May 24, 2021, Project Veritas released a video interview1 with two Facebook insider whistleblowers — a data center technician and a data center facility engineer — who have come forward with internal documents showing how the social media platform is suppressing science and medical facts in the name of combating "vaccine hesitancy."
Facebook recently rolled out a beta test designed to censor negative vaccine information — regardless of its veracity and truthfulness — with the aim of eventually rolling this censorship program in all nations, in as many languages as possible.
The documents prove Facebook is working on behalf of Big Pharma and in coordination with the U.S. Centers for Disease Control and the World Health Organization to protect and promulgate the false narrative that COVID-19 vaccines are safe and effective for everyone. The platform is even hiding posts in which people who dutifully got the shots talk about their adverse effects.
According to the internal documents, Facebook is beta testing a new algorithm that classifies users who post counternarrative information about vaccines into "vaccine hesitancy" (VH) tiers. The users are secretly assigned a "VH score" that dictates whether their posts and comments will be removed, demoted or left alone — regardless of whether they're factually accurate. According to Project Veritas:2
"The insider … revealed the tech giant was running the 'test' on 1.5% of its 3.8 billion users with the focus on the comments sections on 'authoritative health pages.' 'They're trying to control this content before it even makes it onto your page, before you even see it,' the insider [said] …
The stated goal of this feature is to 'drastically reduce user exposure' to VH comments. Another aim of the program is to force a 'decrease in other engagement of VH comments including create, likes, reports [and] replies.'"
Vaccine content is rated based on its perceived ability to "discourage vaccination in certain contexts, thereby contributing to vaccine hesitancy or refusal." According to a "Borderline Vaccine Framework" document, vaccine content is "tiered … by potential harm and how much context is required in order to evaluate harm." The ratings are divided into three primary tiers:3
Depending on where your comment falls within these tiers, your post or comment will be either removed or "demoted" to varying degrees. As noted by investigative journalist and founder of Project Veritas, James O'Keefe, in a Fox News interview:4
"What's remarkable about these private documents … is that 'Tier 2' [violation] says even if the facts are true … you will be targeted and demoted — your comments will be targeted and demoted."
While it's unclear who approved this beta test, the listed authors of the "vaccine hesitancy comment demotion" program are senior software engineer Joo Ho Yeo;5 data scientist Nick Gibian6 who, according to LinkedIn, works on health misinformation and civic harassment; software engineer Hendrick Townley, who states his primary interests are in "harnessing technology and technical understanding towards strengthening our democratic institutions and solving pressing policy issues;"7 machine learning and data scientist Amit Bahl;8 and product manager Matt Gilles.9
The comment demotion strategy that is currently being beta tested is very similar to shadow banning, where a user has been secretly banned — which means none of their followers can actually see their posts — yet they continue posting because they're unaware that the content is not being disseminated.
Under this two-tier information suppression system, you will have no idea whether your posts or comments are being suppressed and can't be seen by other users, and to which degree your post or comment is being suppressed. In general, however, the internal documents reveal that this suppression strategy is currently reducing "vaccine hesitant" comments by 42.5% within the test group.
Now, an example of a "vaccine hesitant" comment is not just "I don't know if I want the vaccine." It also includes comments like, "I saw a study that said someone died who got the vaccine," and personal experiences such as "Excruciating pain after my second vaccine! Shaking so bad, almost to convulsions."
Facebook is even censoring and putting "fake news" labels on data obtained directly from the Vaccine Adverse Event Reporting System (VAERS), which is jointly run by the U.S. Centers for Disease Control and Prevention and the U.S. Food and Drug Administration.
This despite having a public policy to "remove content that repeats … false health information … that are widely debunked by leading health organizations such as the World Health Organization and the CDC."
They justify this by stating that VAERS data and other study findings cannot be communicated unless "full context" is provided. But as noted by the whistleblower, that's a highly ambiguous term. What is full context? Do you have to post an entire study in order for it to be contextual?
In the final analysis, it's clear that Facebook is actively suppressing and censoring science, medical facts and first-hand personal experiences, and in so doing, they are putting the whole world in harm's way. By suppressing crucial information about vaccine risks they are eliminating any possibility of informed consent because it is impossible to understand the risks.
They are promoting ignorance that can, and I firmly believe, will, literally kill many of their users. And, since Facebook openly admits coordinating its censorship with the CDC and WHO, the same can probably be said for both of those organizations. As one of the whistleblowers tells O'Keefe:
"[Zuckerberg wants to] build a community where everyone complies — not where people can have an open discourse and dialogue about the most personal and private and intimate decisions. The narrative [is] get the vaccine, the vaccine is good for you, everyone should get it. If you don't, you will be singled out as an enemy of society."
The second whistleblower, a data center facility engineer, says Facebook is now "prohibiting people from having an open dialogue about issues that affect their personal security." He likens the platform to an abusive partner who doesn't allow their spouse to speak to friends and family about what's going on behind closed doors.
Ironically, leaked video from the same whistleblower shows Facebook CEO Mark Zuckerberg, back in mid-July 2020, expressing his own vaccine hesitancy during a video conference.
"I do just want to make sure that I share some caution on this because we just don't know the long-term side effects of basically modifying people's DNA and RNA," Zuckerberg told his team, referring to COVID-19 vaccines under development.
As noted by O'Keefe, Zuckerberg's own words would now violate his company's public policy and rules of expression.
In related news, Children's Health Defense (CHD) sued Facebook in August 2020, charging the company, its CEO, Zuckerberg, and several fact-checking organizations with "censoring truthful public health posts and for fraudulently misrepresenting and defaming the children's health organization."10 As reported by The Defender, May 25, 2021:11
"The complaint12 alleges Facebook has 'insidious conflicts' with the pharmaceutical industry and health agencies, and details factual allegations regarding the CDC, CDC Foundation and the World Health Organization's extensive relationships and collaborations with Facebook and Zuckerberg, calling into question Facebook's collaboration with the government in a censorship campaign.
Facebook censors CHD's page, targeting factual information about vaccines, 5G and public health agencies. Facebook-owned Instagram deplatformed CHD Chairman Robert F. Kennedy, Jr. on Feb. 10 without notice or explanation.
Lawyers for Children's Health Defense are awaiting the ruling of Judge Susan Illston after defendants' filed a motion to dismiss in the CHD lawsuit alleging government-sponsored censorship, false disparagement and wire fraud."
It seems legal action may be the only way to rein in censorship that has spiraled out of control, and Florida, my home state, is paving the way with brand-new legislation, SB 7072,13 to hold social media companies liable for their censorship. As reported by NBC News, May 24, 2021:14
"Florida Gov. Ron DeSantis … said the bill … cracks down on … social media 'censorship' while safeguarding Floridians' ability to access social media platforms. 'One of their major missions seems to be suppressing ideas that are either inconvenient to the narrative or which they personally disagree with,' DeSantis said …
DeSantis … and others have accused social media companies of censoring conservative thought by removing posts or using algorithms that reduce the visibility of posts …
The bill also imposes hefty financial penalties against social media platforms that suspend the accounts of political candidates. The bill would fine companies $250,000 a day for doing so …
Florida's attorney general can bring action against technology companies that violate the law, under Florida's Unfair and Deceptive Trade Practices Act, and social media platforms found to have violated antitrust law will be restricted from contracting with any public entity, DeSantis said."
The bill also allows private users to sue for certain violations, with statutory damages totaling up to $100,000 per proven claim or actual damages, plus punitive damages "if aggravating factors are present."15
As detailed in "Harvard Professor Exposes Surveillance Capitalism," which features an interview with Shoshana Zuboff, author of the book, "The Age of Surveillance Capitalism," free social media platforms aren't free. You pay with your personal data.
So, not only is Facebook and other social media companies suppressing your freedom of speech — often at the request of government officials, which is illegal — they're also stealing your personal data and using it to control and manipulate you.
Their primary function isn't actually to allow you to communicate with others. Their primary function is surveillance, data collection and social engineering. In other words, you are the commodity, not the other way around. They need you far more than you need them.
Companies like Facebook, Google and third parties of all kinds have the power, and use that power, to target your personal inner demons, to trigger you, and to take advantage of you when you're at your most vulnerable to entice you into action that serves them, commercially or politically.
Your entire existence — even your shifting moods, deciphered by facial recognition software — has become a source of revenue for corporate entities as you're being cleverly maneuvered into doing (and typically buying) or thinking something you may not have done, bought or thought otherwise.
Facebook's massive experiments, in which they used subliminal cues to see if they could make people happier or sadder and affect real-world behavior offline, have proved that — by manipulating language and inserting subliminal cues in the online context — they can change real-world behavior and real-world emotion, and that these methods and powers can be exercised "while bypassing user awareness."
Other technologies, such as digital security systems, employ hidden microphones to spy on your private conversations. All of these data streams, from cell phones, computers, "smart" appliances and video cameras around public areas add to ever-expanding predictive modeling capabilities that, ultimately, are used to control and manipulate you.
As noted by Zuboff, the reason we're in this creepy situation is because there are no laws in place to curtail this brand-new type of surveillance capitalism. Indeed, the only reason it has been able to flourish over the past 20 years is because there's been an absence of laws against it, primarily because it has never previously existed.
Google and Facebook were the only ones who knew what they were doing. The surveillance network grew in the shadows, unbeknownst to the public or lawmakers. The good news is, it's not too late to take back both our privacy — and our freedom of speech online — but we need legislation that addresses the reality of the entire breadth and depth of these systems in their entirety. As noted by Zuboff:16
"The choice to turn any aspect of one's life into data must belong to individuals by virtue of their rights in a democratic society. This means, for example, that companies cannot claim the right to your face, or use your face as free raw material for analysis, or own and sell any computational products that derive from your face …
Anything made by humans can be unmade by humans. Surveillance capitalism is young, barely 20 years in the making, but democracy is old, rooted in generations of hope and contest.
Surveillance capitalists are rich and powerful, but they are not invulnerable. They have an Achilles heel: fear. They fear lawmakers who do not fear them. They fear citizens who demand a new road forward as they insist on new answers to old questions: Who will know? Who will decide who knows? Who will decide who decides? Who will write the music, and who will dance?"
While there's no doubt we need a whole new legislative framework to curtail surveillance capitalism and censorship alike, in the meantime, there are ways you can protect your privacy online and limit the "behavioral surplus data" collected about you. (As of yet, there's not much you can do about online censorship, other than encourage your state legislators to address it, as Florida just began to do.) To protect your privacy, consider taking the following steps:17
Ditch Facebook, Twitter and other social media platforms that siphon your personal data and censor content — Today, there are free-speech alternatives that do neither of those things. |
Use a virtual private network (VPN) to mask the true identity of your computer. |
Do not use Gmail, as every email you write is permanently stored. It becomes part of your profile and is used to build digital models of you, which allows them to make predictions about your line of thinking and every want and desire. Many other older email systems such as AOL and Yahoo are also being used as surveillance platforms in the same way as Gmail. ProtonMail.com, which uses end-to-end encryption, is a great alternative and the basic account is free. |
Don't use Google's Chrome browser, as everything you do on there is surveilled, including keystrokes and every webpage you've ever visited. Brave is a great alternative that takes privacy seriously. Brave is also faster than Chrome, and suppresses ads. It's based on Chromium, the same software infrastructure that Chrome is based on, so you can easily transfer your extensions, favorites and bookmarks. |
Don't use Google as your search engine, or any extension of Google, such as Bing or Yahoo, both of which draw search results from Google. The same goes for the iPhone's personal assistant Siri, which draws all of its answers from Google. Alternative search engines include SwissCows, DuckDuckGo and Qwant. Avoid StartPage, as it has been bought by an aggressive online marketing company which, like Google, depends on surveillance. |
Don't use an Android cellphone, as they are always listening and recording your conversations. |
Don't use Google Home devices — These devices record everything that occurs in your home, both speech and sounds such as brushing your teeth and boiling water, even when they appear to be inactive, and send that information back to Google. |
Regularly clear your cache and cookies. |
Don't use Fitbit, as it has been acquired by Google and will provide them with all your physiological information and activity levels, in addition to everything else that Google already has on you. |
Many people have a sweet tooth. For some, it can become an addiction,1 fueled by a food industry that continually creates an abundance of highly palatable, inexpensive, ultraprocessed foods. As some companies cash in on a market for lab-created, low-calorie sweeteners, one natural sweetener may help curb your sweet tooth without raising your blood sugar. In fact, it may have the opposite effect.
While manufacturers seek out “perfectly engineered food,”2 the incidence of obesity3 and obesity-related health conditions4 has skyrocketed. Type 2 diabetes is one of the obesity-related conditions that has a significant impact on many of your bodily systems.
People with diabetes have a higher risk of also having heart disease, stroke, glaucoma, kidney disease and high blood pressure.5 It would make sense if the incidence of diabetes and obesity goes down, you could have a positive impact on these conditions that contribute to at least five of the top 10 leading causes of death.6
The obesity epidemic is one of the most important global public health challenges. Obesity was linked with 4.7 million premature deaths worldwide in 20177 and according to the National Diabetes Statistics Report, 34.2 million people, or 10.5% of the U.S. population, has diabetes.8 By using this sweetener you may reduce your risk of insulin resistance, a primary symptom of diabetes.
Sugar is a carbohydrate9 found in fruits and vegetables and added to food products. Added sugars are usually sucrose (table sugar) and high-fructose corn syrup (HFCS). Once digestion has started in the stomach, sugars break down into one of three monosaccharides from which other sugars are formed.
These include glucose, fructose and galactose. Glucose is one of the main compounds found in sucrose, lactose and maltose. These are disaccharide sugar compounds commonly found in foods. Fructose is the main type of sugar found in fruits and vegetables and galactose is found mostly in dairy products.
In the West, the most used plant-based sweeteners are sucrose and HFCS, a sweetener made from corn. Evidence shows us that no matter what type of sugar you are consuming, it has a significant effect on your metabolism, even in the healthiest people.
Sugar hides under as many as 61 different names in 74% of processed food products10 and while there are copious numbers of studies over decades demonstrating the damage it does to your health, the industry has managed to bury the evidence and claim it has little to no effect on your health or your weight.
In one 12-week study,11 researchers demonstrated men who ate 650 calories a day of sugar had higher levels of fat in their blood and liver. Interestingly, the researchers separated the two groups into those who had evidence of nonalcoholic fatty liver disease (NAFLD) and those who did not. During the study, each participant followed both diets for 12 weeks.
Lead researcher Bruce Griffin, Ph.D., from the University of Surrey, commented on the results saying,12 "Our findings provide new evidence that consuming high amounts of sugar can alter your fat metabolism in ways that could increase your risk of cardiovascular disease."
Sugar can also affect your brain, mood and behavior. Several studies have found an association between a rising intake of sugar and an increase in rates of depression.13,14,15
Sugar stimulates the release of dopamine,16 which is a neurotransmitter that plays a role in many important pathways, many of which affect your mood. This is why sugar feels so good and why manufacturers use it to drive your behavior. But, like other addictive drugs, sugar is not healthy.
One natural sweetener option is Astrea Allulose. Although the market in Japan is significant,17 it is a relatively little-known alternative sweetener in the West. Allulose is found in small quantities in some fruits such as figs, jackfruit and raisins and was given a generally regarded as safe (GRAS) food designation by the FDA.18
Allulose is a monosaccharide sugar that differs from fructose only at one of the carbon atoms.19 This one change makes a world of difference in the way the molecule acts in the body. It is functionally a carbohydrate and mostly absorbed in the small intestines. However, the majority of allulose is excreted by the kidneys before it is metabolized.20
This means that most of the calories you consume from allulose are excreted through your kidneys before being metabolized. It has only been recently that the FDA21 differentiated allulose from sucrose or HFCS on nutrition labels. Before this, anytime it was added to a processed food, it was simply listed as an added sugar.
Therefore, there was little incentive to include allulose in products. Since allulose has 95% fewer calories than sucrose,22 the FDA allowed manufacturers to exclude it from the total and added sugar counts on nutrition labels.23
The percentage of the monosaccharide that is not metabolized does not contribute to energy or caloric intake. In one animal study, researchers found allulose24 contributes a fraction of 1% of the energy of sucrose.25
The researchers called the energy value “effectively zero” and suggested that this “rare sugar providing zero energy … may be useful in sweeteners for obese people as an aid for weight reduction.”26
In addition to contributing little to no calories, allulose elicits a physiological response in the body that may lower your blood glucose27 and reduce abdominal fat28 and fat accumulation around the liver.29,30 This may reduce the rising number of people who have NAFLD. Allulose can also decrease insulin resistance31 and reduce the potential risk for Type 2 diabetes.32
In an analysis of 40 human trials,33 allulose demonstrated the ability to significantly reduce after-meal insulin response, which the researchers believe “lead to modest improvements on postprandial glucose and insulin regulation.”34
Another study35 engaged 30 people who did not have diabetes. They were given a loading dose of sucrose and then randomized to receive 2.5, 5, 7.5 or 10 grams of allulose. Plasma glucose and insulin levels were measured at 30, 60, 90 and 120 minutes after ingestion. The researchers found that in a dose-dependent manner, allulose reduced plasma glucose and insulin levels.
In other words, allulose not only contributes very little to caloric intake or blood glucose, but it also may help to improve insulin regulation. While there are not yet allulose-specific human studies regarding safety, animal studies36 have not found toxicity even at high doses.
In one nonrandomized controlled trial37 using 30 healthy individuals within a normal BMI range, researchers discovered individuals experienced gastrointestinal (GI) symptoms when the dose reached 0.4 grams per kilogram of body weight (g/kg*BW). Gastrointestinal tolerance testing did not indicate severe diarrhea or other symptoms until the dose read 0.5 g/kg*BW.
The researchers suggest that based on their results a maximum single dose should not be over 0.4 g/kg*BW.38 This means a person who weighs 160 pounds could eat 29 grams of allulose in one serving, which is equivalent to 7.25 teaspoons of sugar, without experiencing GI symptoms.
While there is no immediate toxic effect on the body, evidence does suggest that consistent use may affect the weight of your kidneys and liver, the two organs through which the natural sweetener passes. In a study published in 2019,39 researchers noted that using allulose can prevent obesity, but continuous consumption may increase the weight of the liver and kidneys “without apparent pathological and functional abnormalities.”
The study investigated the potential these parameters could change after the participant no longer consumed allulose. Using an animal model, the researchers fed allulose for four weeks and then a controlled diet without allulose for another 10 weeks. At the end of four weeks the weights of the liver and kidney were higher, but the difference disappeared after the animals were no longer fed allulose.40
HFCS, aka corn sugar, is another common form of sugar found in processed foods. While it’s often cited interchangeably with fructose, actually HFCS and fructose are not the same. Fructose is a simple sweetener found naturally in many fruits and vegetables.41 HFCS, on the other hand, is artificially produced from corn, through a process that involves first turning it into corn starch and then back into a mixture of fructose and glucose.42
But whether it’s simple fructose or HFCS, there is evidence to show this type of sugar causes greater damage than simple glucose or table sugar. This is because fructose does not act like glucose in your body.
In one study,43 a group of postmenopausal overweight or obese women consumed fructose beverages with their meals for 10 weeks. The data showed this practice increased fasting glucose and reduced the insulin response. The researchers concluded that the “present results suggest that long-term consumption of diets high in fructose could lead to an increased risk of CVD [cardiovascular disease].”44
Unfortunately, because HFCS is cheaper and 20% sweeter than regular table sugar, it's used by many food and beverage manufacturers, and it has been shown through numerous studies that it not only can contribute to impaired glucose tolerance,45 cardiovascular disease and diabetes, but also can disrupt your sense of hunger and satiety.46
In regard to diabetes, with one global analysis of 43 countries,47 researchers found in areas where HFCS was highly available, the prevalence of diabetes was 20% higher. The results suggested that increased consumption of HFCS increased the risk of Type 2 diabetes, which was independent of obesity.
In another study,48 men and women were given 24 ounces of either a HFCS- or sucrose-sweetened beverage. Blood and urine samples were collected over six hours and a variety of metabolic biomarkers were measured. The researchers found that HFCS led to significantly different acute metabolic effects than sucrose.
Initially, experts thought fructose would be a better choice because it has a low glycemic index. However, only the liver can metabolize fructose.49 And, as mentioned, consuming fructose also increases your appetite, which ultimately contributes to obesity, diabetes and NAFLD.50
Many sweeteners have side effects, and those from artificial sweeteners are more toxic than others. Research in 200851 revealed that sucralose, also known as Splenda, reduces your gut bacteria by 50% and increases the pH level in your intestines. A study52 from 2018 found sucralose is metabolized and accumulates in fat cells.
Research published in 2016 from the Ramazzini Institute linked Splenda to leukemia.53 Not long after this study was published in a peer-reviewed journal, the company engaged public relations firm Ketchum, notorious for its close work with Monsanto and promotional work for genetically engineered crops.
It appears the marketing ploy worked, as the company reduced the impact of the scientific evidence. By 2017, market research showed the market size for Splenda was valued at $697.4 million and was projected to increase 3% through 2025.54 North America and Asia-Pacific accounted for the majority of the market share.
Originally, it was hoped that artificial sweeteners would help curb cravings for sweets in people who have diabetes. Yet, in one study55 using health participants it took only two weeks for the artificial sweetener to trigger adverse effects on blood sugar levels, which lead study author Richard Young from the University of Adelaide commented on in a press release:56
"This highlights the potential for exaggerated post-meal glucose levels in high habitual NAS [noncaloric artificial sweeteners] users, which could predispose them to developing Type 2 diabetes."
Artificial sweeteners may also increase your risk of weight gain, obesity, metabolic syndrome and other related problems like Type 2 diabetes by inducing "metabolic derangements," according to a report published in the journal Trends in Endocrinology and Metabolism.57
Further research found aspartame (NutraSweet), another artificial sweetener, is associated with greater glucose intolerance in people with obesity.58 These are only some of the side effects of artificial sweeteners, which increase your risk of challenging health conditions and are not a safe alternative to table sugar.
You can find more information about Splenda in “Beware the Latest ‘Diet’ Fad: Artificial Sweeteners Fortified With Vitamins and Minerals” and “Research Reveals Shocking Information About Sucralose (Splenda) Side Effects.”
The article "Top 8 Tips to Optimize Your Blood Sugar Level" lists some of the top ways you can take control of your health and reduce your risk of diabetes. The following articles offer some dietary suggestions that may help your body regulate glucose:
1 If you've already had COVID-19, viral antigens may persist in your body that, when reactivated by a COVID-19 vaccine-induced immune response:
The immune response reactivated by the COVID-19 vaccine may trigger inflammation in tissues where the viral antigens are present. Learn more.
2 The spike proteins on the SARS-CoV-2 virus damage endothelial cells by:
When the S protein attached to the ACE2 receptor, it disrupted signaling to the mitochondria and caused damage and fragmentation. The alterations in mitochondrial function were confirmed as part of the inhibition of ACE2 signaling in the lab. Learn more.
3 May 11, 2021, Sen. Rand Paul questioned Dr. Anthony Fauci on the NIAID's funding of gain-of-function research on bat coronaviruses, some of which was conducted at the Wuhan Institute of Virology (WIV). Which of the following did The National Pulse discover had quietly occurred in late March?
Shortly after Fauci's testimony, the WIV deleted mentions of its collaboration with the NIAID/NIH and other American research partners from its website. It also deleted descriptions of GoF on the SARS virus. Learn more.
4 Which of the following now appears to be one of the key reasons for why COVID-19 vaccines are causing so many side effects and likely will cause neurological and vascular problems in the future?
A key problem with all of these gene-based COVID-19 vaccines is that the spike protein itself appears toxic, and your body is now a spike protein-producing factory. Its inherent toxicity may be due to it being a prion protein. If so, we can expect these injections to cause all manner of prion diseases, such as Alzheimer's, Parkinson's and Lou Gehrig's disease (ALS). Learn more.
5 NVIC does not make vaccine use recommendations but, rather, encourages you to make:
NVIC does not make vaccine use recommendations but, rather, supports the availability of all preventive health care options, and encourages you to make educated decisions when it comes to your health. Learn more.
6 Which of the following parts of SARS-CoV-2 is responsible for the worst symptoms of COVID-19 and causes the most damage?
The worst symptoms of COVID-19 are created by the SARS-CoV-2 spike protein, and that is the very thing gene-based COVID vaccines are instructing your body to make. Learn more.
In this interview, Stephanie Seneff, Ph.D., and Judy Mikovits, Ph.D., a dream-team in terms of deep insights into the scientific details, explain the problems they see with gene-based COVID-19 vaccines. There is a load of highly useful technical information that you can use to defend your opposition to these dangerous vaccines.
However, unless you have deeply studied molecular biology and genetics, it would be wise to view the video two or three times, as with each review, you will learn more and understand just how dangerous these vaccines are. I recently interviewed Seneff about the excellent paper1 she published on this topic. That interview was featured in “COVID Vaccines May Bring Avalanche of Neurological Disease.”
In May 2020, I also interviewed Mikovits about the possibility of these vaccines causing reproductive harm and other health problems. At the time, Mikovits warned that fertility rates may drop thanks to the SARS-CoV-2 spike protein creating antibodies that attack syncytium, and indeed, we’re now starting to see that.
Still, the U.S. Centers for Disease Control and Prevention are recommending pregnant women get these vaccines, as well as children as young as 12, which is unconscionable, considering the potential lifelong risks and impairment of fertility.
As noted by Mikovits, we now know that the worst symptoms of COVID-19 are created by the SARS-CoV-2 spike protein, and that is the very thing these gene-based vaccines are instructing your body to make. But it’s far worse, as the vaccines do not cause your body to make the same spike protein as SARS-CoV-2 but one that has been genetically modified, making it far more toxic. So, it’s no wonder things are going wrong.
“The SARS-CoV-2 infection never was what they said it was,” Mikovits says. “There was no infection asymptomatically. It's a monkey virus coming out of a monkey cell line and that's the problem, but the spike protein is clearly [causing] the disease.
So, you just injected the envelope of HIV … a syncytin gammaretrovirus envelope, and a SARS S2 receptor binding domain. That's not a vaccine. It is the disease-causing agent. It's a bioweapon. So now your cells are all producing that bioweapon and you're going to take out the innate immunity, NK [natural killer] cells and dendritic cells …
You're going to disrupt your white blood cells, your immune response. You're going to turn on an anti-inflammatory cytokine signature in every cell of your body. It exhausts your NK cells' ability to determine infected cells. It's the nightmare we predicted.”
In her paper, “Worse Than The Disease: Reviewing Some Possible Unintended Consequences of mRNA Vaccines Against COVID-19,” published in the International Journal of Vaccine Theory, Practice and Research in collaboration with Dr. Greg Nigh,2 Seneff explains that a significant part of the problem is that while the natural spike protein is bad, the spike protein your body produces in response to the vaccine is even worse.
The reason for this is because the synthetic RNA has been manipulated in such a way as to create a very unnatural spike protein that result in it not collapsing on itself into the cell once it attaches to the ACE2 receptor, as it normally does. Instead it stays open and attached to the ACE2 receptor, disabling it and causing a host of problems leading to heart, lung, and immune impairment. As explained by Seneff:
“They modified the RNA to make it really sturdy so the enzymes can't break it down … Normally, enzymes that are in your system would just break down that RNA. RNA is very fragile, but they've made it sturdy by putting in PEG [polyethylene glycol], by adding this lipid membrane, and the lipid is positively charged, which causes the cell to be very upset when that goes into the membrane of the cell.
But I think maybe the most disturbing thing is they actually modified the [RNA] code so that it doesn't produce a normal version of the spike protein. It produces a version that has a couple of prolines in it, side by side at the critical place where this spike protein normally would fuse with the cell that it's infecting.
So, the spike protein binds to the ACE2 receptor once it's produced by the human cell … but it's a modified version of the spike protein. It has these two prolines that make it very stiff so that it can't reshape. Normally it would bind to the ACE2 receptor and then it would reshape and go straight into the membrane like a spear.
Because of this redesign, it can't do that, so it sits there on the ACE receptor, exposed … That allows the immune cells to produce antibodies specific to that place where it should be fusing with the cell, the fusion domain. It messes up the fusion domain, keeps the protein open, and prevents the protein from getting in, which means the protein will just stick there on the ACE2 receptor, disabling it.
When you disable ACE2 receptors in the heart, you get heart failure. When you disable them in the lungs, you get pulmonary hypertension. When you do it in the brain, you get stroke. Lots of nasty things happen when you disable ACE2 receptors …
The other thing they've done with the RNA is they've stuck in a lot of extra Gs (guanine) and Cs (cytosine), which makes it much better at making proteins. It's turned up the gain on the natural virus 1,000-fold, making the RNA much more willing to make a protein. So, it'll make a lot more spike protein than you would've had from a natural RNA virus.”
With the added information provided by Seneff, Mikovits now believes the reality of these vaccines may be exponentially worse than she initially predicted a year ago. Not only is the lipid nanoparticle a serious hazard, as we’ve seen with Gardasil and some of the newer hepatitis B vaccines, but we now also have the added issue of unnatural mRNA, made more robust so as to evade its natural breakdown.
As explained by Mikovits, free RNA acts as a danger signal inside your body, so now your system is on red alert for however long the RNA remains viable. Now, by manipulating the RNA code to be enriched in G and C, and configured as if it’s a human messenger RNA molecule ready to make protein by adding a polyA tail, the spike protein’s RNA sequence in the vaccine looks as if it is part bacteria,3 part human4 and part viral at the same time.
“We use poly(I:C) [a toll-like receptor 3 agonist] to signal the cell to turn on the type I interferon pathway,” Mikovits explains, “and because this is an unnatural synthetic envelope, you're not seeing poly(I:C), and you're not [activating] the Type I interferon pathway.
You've bypassed the plasmacytoid dendritic cell, which combined with IL-10, by talking to the regulatory B cells, decides what subclasses of antibodies to put out. So, you've bypassed the communication between the innate and adaptive immune response. You now miss the signaling of the endocannabinoid receptors …
A large part of Dr. [Francis] Ruscetti’s and my work over the last 30 years has been to show you don't need an infectious transmissible virus — just pieces and parts of these viruses are worse, because they also turn on danger signals. They act like danger signals and pathogen-associated molecular patterns.
So, it synergistically leaves that inflammatory cytokine signature on that spins your innate immune response out of control. It just cannot keep up with the myelopoiesis [the production of cells in your bone marrow]. Hence you see a skew-away from the mesenchymal stem cell towards TGF-beta regulated hematopoietic stem cells.
This means you could see bleeding disorders on both ends. You can't make enough firetrucks to send to the fire. Your innate immune response can't get there, and then you've just got a total train wreck of your immune system.”
With respect to Mikovits’ comment that pieces and parts of the virus are actually worse than the whole virus, that is precisely what we have with the COVID vaccines. In last week’s interview with Seneff, she explained how the manufacturing process leaves fragmented genetically modified RNA in the vaccine. They are not filtered out and assumed to be harmless, but as Mikovits states, this is not the case. This is being completely missed as one reason why this vaccine is so dangerous.
As noted by Seneff, her and Mikovits’ findings mesh well to explain many of the problems we’re now seeing from these gene-therapies. For example, vaccinated patients are reporting herpes and shingles infection following COVID-19 vaccination, which you’d expect if your Type I interferon pathway is disabled.
“Basically, you've got these latent viruses that are not bothering you at all until your immune system gets completely distracted by this crazy thing going on in the spleen with all this messenger RNA and all these spike proteins,” Seneff says.
“Immune cells are distracted from their other job of keeping these viruses in check. So, you get these other conditions showing up, and there are several. There's Bell’s palsy (facial palsy), for example. There are over 1,200 cases of Bell's palsy reported after the vaccine in the Vaccine Adverse Event Reporting System (VAERS).
And when you look at the research of what causes that, they really point to the herpes virus and the varicella virus as being the source of Bell's palsy. The Type I interferon system is what you need to keep these guys in check, and so those viruses are getting enabled and they're causing symptoms.
That is actually a very bad sign. If a woman who's pregnant has a herpes flare-up during pregnancy, she has a twofold increased risk of producing an autistic son.
Also, in a study on 200 Parkinson's patients, compared to 200 age- and gender-matched controls, six of those Parkinson's patients had at least one episode of Bell's palsy in the past, whereas none of the controls had. So, it looks to me like the Bell's palsy is an indicator of a future risk of Parkinson's disease.”
To summarize, it looks as though pregnant women who are getting the COVID-19 vaccine are at increased risk not only for miscarriage but also for future infertility and having an autistic child. So, please, be careful out there and spread the word.
The best way to treat any disease is to prevent it. These vaccines simply are not decreasing COVID-19 but radically decreasing the health of those who receive it, especially pregnant women that the CDC merely a month ago encouraged to get vaccinated without a shred of safety evidence.
Mikovits has done a great deal of research on interferon for the last 40 years. Innate immune interferon makes up your entire frontline defense. People with HIV/AIDS have dysregulated Type I interferon, which allows parasites to gain a solid foothold. Interestingly enough, antiparasitic drugs such as hydroxychloroquine and ivermectin have been shown to be effective against COVID-19, both prophylactically and in treatment.
Mikovits cites a research paper5 titled “War and Peace Between Microbes,” which details how HIV-1 interacts with coinfecting viruses, thereby accelerating the disease. Herpes viruses in particular have been implicated as a cause of AIDS. Human herpesvirus 6 (HHVS-6) has also been implicated in myalgic encephalomyelitis or chronic fatigue syndrome (ME-CFS).
In short, these diseases, AIDS and ME-CFS, don’t appear until viruses from different families partner up and retroviruses take out the Type 1 interferon pathway.
In short, the COVID-19 vaccines are capable of causing damage in a number of different ways. Disturbingly, all these different mechanisms of harm have synergistic effects when it comes to dysregulating your innate and adaptive immune systems and activating latent viruses. “It's just an explosion of a nightmare of crippling every area of your immune response,” Mikovits says.
According to Mikovits, there’s evidence showing the SARS-CoV-2 spike protein was engineered by integrating HIV and XMRV proteins. XMRV stands for xenotropic murine leukemia virus-related virus, a human retrovirus that is very similar to endogenous retroviruses also found in other mammals.
XMRV has been linked to ME-CFS. HIV, which can cause AIDS, is another human retrovirus (although as mentioned earlier, HIV does not appear to trigger AIDS all by itself. It needs a coinfection.)
“Our endogenous gammaretrovirus is called human endogenous retrovirus-W (HERV-W). HERVW is all the way back in genesis in our original endogenous genome. It's a gammaretrovirus that expresses only the envelope, because in retroviruses, the envelope alone is enough to cause the disease. That envelope protein is called syncytin. They're [now] calling it ‘spike protein’ just to throw us all off,” Mikovits says.
According to Mikovits, the SARS-CoV-2 virus was created by introducing a mutation into a molecular clone. Vero E6 monkey tissues are known to be infected with SIV and other gammaretroviruses, and the SARS-CoV-2 virus has markers suggesting it was grown in a Vero E6 cell line, she says.
“So syncytin is the gammaretrovirus; it cross-reacts with the mouse and monkey gammaretroviruses. Monkeys, mice all have syncytin. Endogenous viruses express, especially during hormonal cycles. When it's expressed in the wrong place, like in the brain or the spinal cord, it's long been associated with the inflammatory disease and the destruction of the myelin sheet in multiple sclerosis (MS).
So, syncytin expressed it in the wrong place gives you the paralytics diseases. We know Parkinson's is associated with Type I interferon responses. We're now starting to appreciate that there is low-level expression of our endogenous virome all the time, and that in our innate immune response it's trying to shape and educate our Type I interferon pathways …
The final and biggest problem is these exosomes, because your body's exosomes are like your cells' response to express its regulatory RNAs, small inhibitory RNAs, long-chain non-coding RNA — which Ritchie Shoemaker has long associated with chronic Lyme and ME/CFS — and the TGF-beta I pathway.
TGF-beta I, that's the master switch to turn on which Type I interferon, which [is needed for] myelopoiesis. But these exosomes are packaging not only RNA that you're making, but now you've dysregulated the methylation so you've woken up your endogenous virome, and then syncytin is going to be expressed.”
In her paper, Seneff also describes how mRNA can, in fact, alter your DNA, essentially integrating the instructions to make spike proteins into your genome. Typically, mRNA cannot be integrated directly into your genes because you need reverse transcriptase.
Reverse transcriptase converts RNA back into DNA (reverse transcription). However, there’s a wide variety of reverse transcriptase systems already embedded in our DNA, which makes this possible. This is an area that Mikovits has studied for decades, so, commenting on Seneff’s findings, she says:
“When you activate latent and defective viruses, you turn on reverse transcriptase; you turn on the virome. But you also need an integrase gene. So how are retroviruses silenced? [Through] DNA methylation. [When] you throw in a lot of GC-rich regions — you've got that synthetic viral particle [i.e., the vaccine-induced spike protein RNA] — now you've woken up your herpes viruses.
[Latent viruses] are silenced [through] DNA methylation, but as our soil is depleted in minerals, we have people with methylation defects. This is why I said the first people who are going to die are people with inflammatory conditions and cancer.”
In her paper, Seneff also discusses evidence suggesting the SARS-CoV-2 spike protein may be a prion, which is yet another piece of really bad news. “It’s absolutely terrifying to me,” she says, adding:
“I'm now thinking that may be the worst aspect of these mRNA vaccines, because they're producing this abnormal spike protein that doesn't want to go into the membrane. Prion proteins are known to be membrane proteins. They're alpha-helices in the membrane and then they misfold, becoming beta-sheets in the cytoplasm, and that's what leads to the prion problem.
They form a crystal that draws in other proteins and makes this big mess and builds fibrils and Alzheimer's plaque. The main prion protein is PrP, which is in Creutzfeldt-Jakob disease, the human form of mad cow disease. It's a sort of protein-source infection. It's quite wild because there's no DNA involved, no RNA involved, just protein.
But the thing is, when you have produced a version of mRNA that knows how to spew out tons of a prion protein, the prion proteins become problematic when there's too many of them and the concentration is too high in the cytoplasm.
And the spike proteins that these mRNA vaccines are producing … isn't able to go into the membrane, which I think is going to encourage it to become a problematic prion protein. Then, when you have inflammation, it upregulates alpha-synuclein [a neuronal protein that regulates synaptic traffic and neurotransmitter release].
So, you're going to get alpha-synuclein drawn into misfolded spike proteins, turning into a mess inside the dendritic cells in the germinal centers in the spleen. And they're going to package up all this crud into exosomes and release them. They’re then going to travel along the vagus nerve to the brainstem and cause things like Parkinson's disease.
So, I think this is a complete setup for Parkinson's disease. What may happen is that because they got this vaccine, they get Parkinson's disease five years earlier than they would have gotten it otherwise. It's going to push forward the date at which someone who has a propensity towards Parkinson's is going to get it.
And it's probably going to cause people to get Parkinson's who never would have gotten it in the first place — especially if they keep getting the vaccine every year. Every year you do a booster, you bring the date that you're going to get Parkinson's ever closer.”
Two of the four COVID-19 vaccines on the market in Europe and the U.S., AstraZeneca and Johnson & Johnson, are using viral vectors and DNA rather than using nanolipid-coated mRNA. Unfortunately, while potentially slightly less dangerous than Moderna’s and Pfizer’s mRNA versions, they can still cause significant problems through mechanisms of their own. As explained by Mikovits:
“As mentioned, it's an adenovirus vector expressing the protein. So, the HIV, the XMRV envelope, the syncytin, the HERV-W envelope and the ACE2 are already being expressed in the vector.
With respect to the RNA component, it's less dangerous because you're not going to see much of the mechanisms we've been talking about. But these adenovirus vector protein-producing vaccines are grown in an aborted fetal tissue cell line, so now you've got human syncytin [in there]. You've got 8% of the human genome of another human.
So, again, looking at the communication that has to regulate your Type I interferon response, it’s going to give you autoimmunity. In immunocompromised people, it's going to continue to express and that will give you a live infection, and you already have your firetrucks fighting another [infection]. You can't fight a war on three fronts.
I say, ‘You only need one shot because it's the most toxic.’ It’s the most toxic in that sense. We have many mechanisms to degrade RNA, and we can restore methylation machinery. It's a nightmare, but I believe our immune system can break it [the synthetic vaccine mRNA) down.”
Disturbingly, it appears the COVID-19 vaccines may also cause trouble for those who decide not to get the shots but spend time in close proximity to people who did. While it cannot be viral shedding, as none of the vaccines use live or even attenuated virus, there appears to be some sort of spike protein transmission going on.
While the spike protein cannot replicate or multiply like a virus, it is toxic in and of itself. In her paper, Seneff details how the spike protein acts as a metabolic poison, capable of triggering pathological damage leading to lung damage and heart and brain diseases:6
“In a series of papers, Yuichiro Suzuki in collaboration with other authors presented a strong argument that the spike protein by itself can cause a signaling response in the vasculature with potentially widespread consequences.
These authors observed that, in severe cases of COVID-19, SARS-CoV-2 causes significant morphological changes to the pulmonary vasculature … Furthermore, they showed that exposure of cultured human pulmonary artery smooth muscle cells to the SARS-CoV-2 spike protein S1 subunit was sufficient to promote cell signaling without the rest of the virus components.
Follow-up papers showed that the spike protein S1 subunit suppresses ACE2, causing a condition resembling pulmonary arterial hypertension (PAH), a severe lung disease with very high mortality …
Suzuki et al. (2021) went on to demonstrate experimentally that the S1 component of the SARS-CoV-2 virus, at a low concentration … activated the MEK/ERK/MAPK signaling pathway to promote cell growth. They speculated that these effects would not be restricted to the lung vasculature.
The signaling cascade triggered in the heart vasculature would cause coronary artery disease, and activation in the brain could lead to stroke. Systemic hypertension would also be predicted. They hypothesized that this ability of the spike protein to promote pulmonary arterial hypertension could predispose patients who recover from SARS-CoV-2 to later develop right ventricular heart failure.
Furthermore, they suggested that a similar effect could happen in response to the mRNA vaccines, and they warned of potential long-term consequences to both children and adults who received COVID-19 vaccines based on the spike protein.
An interesting study by Lei et. al. (2021) found that pseudovirus — spheres decorated with the SARS-CoV-2 S1 protein but lacking any viral DNA in their core — caused inflammation and damage in both the arteries and lungs of mice exposed intratracheally.
They then exposed healthy human endothelial cells to the same pseudovirus particles. Binding of these particles to endothelial ACE2 receptors led to mitochondrial damage and fragmentation in those endothelial cells, leading to the characteristic pathological changes in the associated tissue.
This study makes it clear that spike protein alone, unassociated with the rest of the viral genome, is sufficient to cause the endothelial damage associated with COVID-19. The implications for vaccines intended to cause cells to manufacture the spike protein are clear and are an obvious cause for concern.”
As explained by Mikovits, the transmission that appears to be occurring from vaccinated individuals to unvaccinated ones is the transmission of exosomes, basically, the spike protein. The problem is these exosomes look like a virus to your immune system, and “If that synthetic nanoparticle is a virus-like particle and they're literally self-assembling, then you've got yourself a synthetic nightmare,” she says.
As for which vaccine might be the most dangerous, Mikovits believes the vector-based DNA vaccines (AstraZeneca and Johnson & Johnson) are the most dangerous for those with chronic Lyme disease or any inflammatory disease associated with an abnormal host immune response, such as shingles, viral infections or cancer, women who have already received the Gardasil vaccine (as this may predispose them to problems with the lipid nanoparticle), and those with Parkinson’s or Huntington-like diseases.
Seneff, meanwhile, worries that children may be susceptible to either type of COVID vaccine, simply because they’ve already received so many different vaccines. Mikovits agrees, but believes the mRNA vaccines may be more harmful in this age group:
“The most dangerous to the children are the mRNA vaccines because their immune systems are growing, growing, growing, growing. You introduce or you turn on a fire, what happens? All the stem cells that are important for growing that say, ‘OK, all is calm in the immune system, go build bone, go build brain cells, go do the pruning with the macrophages.’ You can't have your macrophages clearing all the viruses.
And yes, reverse transcriptase is ‘on,’ it's expressed in telomeres. You're growing. That's the whole idea of everything. All the brakes are off. Same thing in pregnancy. That's why we don't do anything in pregnancy because you've got to stay unmethylated in order to respond to your environment, that endogenous genome of the virome. That's your Type I interferon responses.
You don't want myelopoiesis, you want embryonic development. We're going to see things like Down syndrome … Rett syndrome. Rett syndrome, that's inappropriate DNA methylation in little girls. So, for the kids, the worst thing in the world is the RNA vaccines.”
While the variety of diseases we may see a rise in as a result of this vaccination campaign are myriad, some general predictions can be made. Seneff believes we’ll see a significant rise in cancer, accelerated Parkinson's-like diseases, Huntington's disease, and all types of autoimmune diseases and neurodegenerative disorders.
Mikovits suspects many will die rather rapidly. “We have evidence in the HTLV-1 associated myelopathy that these things go from long latency periods to [putting] you in a wheelchair in six months,” she says. “So, with all these other toxins combined hitting you, it's not going to be ‘live and suffer forever.’ It's going to be suffer five years and die.”
She likens the COVID-19 vaccines to a “kill switch” for all who have been previously injured by vaccines, whether they actually realize it or not. As noted by Mikovits, it’s been shown that 6% of the American population are asymptomatically infected with XMRVs and gammaretroviruses from contaminated vaccines. The COVID shot will effectively accelerate their death by crippling their immune function. “The kids that are highly vaccinated, they're ticking time bombs,” she says.
While all of this is highly problematic, there is help. As noted by Mikovits, remedies to the maladies that might develop post-vaccination include:
Hydroxychloroquine and ivermectin treatments |
Low-dose antiretroviral therapy to reeducate your immune system |
Low-dose interferons such as Paximune, developed by interferon researcher Dr. Joe Cummins, to stimulate your immune system |
Peptide T (an HIV entry inhibitor derived from the HIV envelope protein gp120; it blocks binding and infection of viruses that use the CCR5 receptor to infect cells) |
Cannabis, to strengthen Type I interferon pathways |
Dimethylglycine or betaine (trimethylglycine) to enhance methylation, thereby suppressing latent viruses |
Silymarin or milk thistle to help cleanse your liver |
From my perspective, I believe the best thing you can do is to build your innate immune system. To do that, you need to become metabolically flexible and optimize your diet. You’ll also want to make sure your vitamin D level is optimized to between 60 ng/mL and 80 ng/mL (100 nmol/L to 150 nmol/L), ideally through sensible sun exposure. Sunlight also has other benefits besides making vitamin D.
Use time-restricted eating and eat all your meals for the day within a six- to eight-hour window. Avoid all vegetable oils and processed foods. Focus on certified-organic foods to minimize your glyphosate exposure, and include plenty of sulfur-rich foods to keep your mitochondria and lysosomes healthy. Both are important for the clearing of cellular debris, including these spike proteins. You can also boost your sulfate by taking Epsom salt baths.
To combat the toxicity of the spike protein, Seneff suggests optimizing autophagy, which may help digest and remove the spike proteins. Time-restricted eating will upregulate autophagy, while sauna therapy, which upregulates heat shock proteins, will help refold misfolded proteins. They also tag damaged proteins and target them for removal.
It is important that your sauna is hot enough (around 170 degrees Fahrenheit) and does not have high magnetic or electric fields. Last but not least, Mikovits recommends never getting another vaccination.
“We knew the flu shot would drive the disease,” she says. “It's the combinations. That's a ticking time bomb sitting there in every cell. So never get another vaccine and be very careful about drugs that compromise your immune system.
The answer is, don't hyper-immune activate. Don't eat GMO. Don't ingest it and don't inject it. And don't put it on your skin. Don't use toxins on your hair. Use essential oils, use antimicrobials … ozonated balms and creams break apart the lipid particles, cannabis balms and creams normalize skin, [which is part of] your immune system …
Remember, immune dysfunction accelerates every time you add an immune activation event. So, if the entire world never again took another shot, even the most susceptible populations, they could stay well … We really have to say no more shots because they're the single biggest toxin to anyone, and an immune dysregulator.”
I recently had the opportunity to be a guest on Mikhaila Peterson’s “Opposing Views” on the topic of COVID-19. Open debate and sharing of information from all sides is so important, especially now that censorship of certain groups, organizations and individuals — in direct violation of Constitutional law — is rampant.
The other guest featured was Jeremy Kamil, Ph.D., an associate professor of microbiology and immunology at LSU Health Shreveport, who has studied the herpes virus for two decades and has a passion for studying how viruses work. Peterson said she emailed 20 doctors to get views from the conventional medical community on COVID-19 — and Kamil was the only one who agreed to be on the show.
I encourage you to watch the video in full and make up your own mind about what you hear, but as I didn’t get a chance to respond to Kamil’s statements directly, I’d like to do that now, as well as provide a recap of some of the most important take-away points from the interview.
When talking about COVID-19, it’s important to start at the beginning — not the start of the pandemic but Event 201, which took place in October 2019.
Representatives from the World Economic Forum, the Centers for Disease Control and Prevention, Johns Hopkins University Population Center, the World Bank, the Chinese government and vaccine maker Johnson & Johnson were among those at the event, which was organized by Bill Gates and, too coincidentally, simulated a worldwide pandemic triggered by a novel coronavirus.1,2
Mirroring what is now occurring, social media censorship was a prominent strategy used at the event to protect the dissemination of vaccine propaganda and the narrative surrounding the global event. If you are considering brushing this off as “conspiracy theory,” you can read about Event 201 for yourself at its official site.3
Peterson and I discussed a bit about Gates, and you may be wondering why I’m bringing him up. It’s part of understanding the immense power and control being wielded by private individuals and the ultimate goal of technocratic tyranny. When the U.S. withdrew funding from the World Health Organization in 2020, Gates became the biggest funder of the WHO.
The two — Gates and the WHO — have been instrumental in pushing for a global vaccination campaign, and Gates has a great deal of money invested in these vaccines. The WHO is the tool that was used to implement a global shutdown — a catastrophe — in 2020, with the end goal being wealth transfer, economic destruction and societal reformation.
It is also interesting that Gates and company have restricted access to this highly profitable vaccine only to countries that can afford it. The patents have not been shared with other countries so they could get this “lifesaving” vaccine, which clearly emphasizes that the primary purpose of this vaccine is not to save lives but to make large profits.
Gates isn’t the only player — there are many others, including Google and founder and executive chairman of the World Economic Forum (WEF) Klaus Schwab, who first started circulating the idea of The Great Reset. Kamil said he wasn’t familiar with the term, which is something I’d urge him to read up on as he formulates his opinions.
I also touched briefly on the overwhelming evidence suggesting that SARS-CoV-2 is an engineered virus that leaked from the Wuhan Institute of Virology (WIV), which was conducting gain-of-function research on coronaviruses, funded by Dr. Anthony Fauci.4 It’s a lot to take in, I know, especially if this is the first you’re hearing about it, but as the pieces of the puzzle come together, it becomes obvious what is really going on.
When asked about the mysterious disappearance of flu during the 2020-2021 season, Kamil stated it’s because “masks are really effective [at] suppressing viral transmission.” If that’s the case, then why didn’t COVID-19 cases similarly disappear? The next rational question is, were flu cases and deaths simply reallocated as COVID-19 deaths?
Up until around July 2020, the U.S. Centers for Disease Control and Prevention (CDC) counted flu and pneumonia deaths separately, but then began reporting a combination of pneumonia, flu and COVID deaths, under a new category listed as "PIC" (Pneumonia, Influenza, COVID), via their COVIDView webpage.5
February 12, 2021 — toward the end of peak flu season in the U.S. — COVIDView was replaced with the COVID Data Tracker Weekly Review, which no longer appears to mention flu and pneumonia.6
As for the effectiveness of masks — and the absurdities surrounding their use during activities like swimming — there’s a wealth of evidence that masks are ineffective. Only one randomized controlled trial has been conducted on mask usage and COVID-19 transmission, and it found masks did not statistically significantly reduce the incidence of infection.7
A working paper from the National Bureau of Economic Research8 found that nonpharmaceutical interventions, such as lockdowns, quarantines and mask mandates, have not significantly affected overall virus transmission rates.9
When asked what the “proper” response to the pandemic would be, Kamil said, “It has to be driven by case numbers.” This sounds good in theory, provided the case numbers you’re basing recommendations on are accurate — and the resulting recommendations are in line with the severity of the disease and individual risk assessments. But, in the case of COVID-19, they most often were not.
What evidence is there that the case numbers were manipulated? PCR tests recommended by the WHO used to be set to 45 cycle thresholds (CTs),10 yet the scientific consensus has long been that anything over 35 CTs renders the test useless,11 as the accuracy will be a measly 3%, with the other 97% being false positives and artificially driving up case numbers.
Then, one hour after Joe Biden’s inauguration as the 46th president of the United States, January 20, 2021, the WHO — suddenly and out of the blue — lowered the recommended PCR CT,12 which automatically guaranteed that the number of “cases,” i.e., positive PCR test results, would plummet.
And this isn’t even getting into how the CDC changed how COVID-19 is recorded on death certificates in March 2020, de-emphasizing preexisting conditions and comorbidities, and basically calling all deaths in which the patient had a positive SARS-CoV-2 test a COVID-19 death.
Another one of Kamil’s points was to avoid getting data from “someone trying to sell you something.” I would agree, only Kamil used the example of someone “selling a health supplement online,” ignoring the fact that the real profiteers in this pandemic are not people selling supplements online but billionaires who are only getting richer.
Stéphane Bancel, CEO of Moderna, now has a net worth of $5.3 billion,13 to give one example. He joined the billionaires club April 2, 2020, when news that phase 2 trials of Moderna’s COVID vaccine were set to begin, driving up its stock.14
Meanwhile, Pfizer’s COVID vaccine has already generated $3.5 billion in revenue in the first three months of 2021,15 and the company said it expects “durable demand” for the vaccine to continue in coming years, similar to flu vaccines. Estimates suggest revenue will reach $26 billion for Pfizer’s COVID vaccine by the end of 2021.16
So, following Kamil’s own advice, Pfizer and Moderna would be among those to not trust, based on their making billions, which is exponentially more than any supplement manufacturer is making. But even putting profits aside, as I told Peterson, one point that should give anyone pause before trusting a company would be if it has a criminal history of fraud and selling dangerous products — of which both Pfizer and Johnson & Johnson can attest to.
Kamil made some statements that I strongly disagree with, one of them being that if you get a COVID-19 vaccine “it’s almost 100% impossible for you to die from COVID — even if you caught like the scariest variants we know of.” This is simply not true. As of April 26, 2021, there have been 9,245 reported cases of COVID-19 in fully vaccinated individuals, including 132 deaths.17 This is from the CDC’s own data.
There’s also a risk of death from the COVID-19 vaccine. According to the U.S. Vaccine Adverse Event Reporting System (VAERS), as of April 23, 2021, there have been 3,544 deaths reported following COVID-19 vaccination.18 Past investigations have shown only between 1%19 and 10%20 of adverse reactions are ever reported to VAERS, which is a passive, voluntary reporting system, so the actual number could be much higher.
Kamil also suggested that if you’re healthy, it makes no difference in terms of getting sick from COVID-19 because “viruses like healthy cells” and “they love a healthy [cell] just like a person might, if you're a carnivore, might like a juicy steak.”
This seriously undermines the power that you have to take control of your health, because, in reality, it’s well known that people who are unhealthy, with underlying conditions, are far more likely to contract and die from COVID-19. Your state of health absolutely matters.
Kamil also seems to be seriously misguided about health organizations like the U.S. Food and Drug Administration, stating that it doesn’t “make a dollar more” by approving a vaccine and describing it as “one of the best organizations, like, as far as protecting your health and watching out for, like, Americans.”
While the FDA itself does not accept corporate money, it does receive money funneled via a nonprofit foundation, which in turn receives money from other nonprofits funded by private interests. It’s really all a façade because the end result is the same. Those donating the money ultimately end up with the ability to pull strings, when needed. The FDA’s conflicts of interest and failures to act on behalf of Americans’ best interests are also well noted.
The pandemic has succeeded in generating fear and controlling human behavior, and anything that counters its final solution of vaccination is being censored — this is a clue that shouldn’t be overlooked. Vaccine passports are also being offered as part of this solution, as a tool to get your freedom back, but it’s at the price of — your freedom.
Imagine a world in which you cannot travel, go to a sports event, enter your workplace or even a grocery store unless you have the proper credentials. If it sounds like history repeating itself in the most horrific way, you’re not far off. Even open debate is being silenced, and it’s impossible to give informed consent to vaccination if you only know one side. When you only have one side to the story, then that’s propaganda, not real information.
Peterson asked me one very important question, which was what should people be doing to stay healthy. One key strategy is to be metabolically flexible, and my No. 1 recommendation to do so is to remove linoleic acid from your diet.
Omega-6 linoleic acid (LA) is a pernicious metabolic poison that is highly susceptible to oxidation, and as the fat oxidizes, it breaks down into harmful subcomponents such as advanced lipid oxidation end products (ALES) and oxidized LA metabolites (OXLAMS). These ALES and OXLAMS also cause damage. To avoid LA, which is linked to chronic degenerative disease, you need to avoid all vegetable oils and eliminate virtually all processed foods and restaurant foods from your diet.
Other strategies to build immunity include optimizing vitamin D. My peer reviewed study, published in the journal Nutrients in October 2020,21 demonstrates the clear link between vitamin D deficiency and severe cases of COVID-19.
I also recommend familiarizing yourself with nebulized hydrogen peroxide, which can be used not only to improve symptoms but as a routine maintenance strategy to support optimal health. You can hear the rest of the interview in its entirety, including the unique risks posed by mRNA vaccines, by watching the video above.