Trending Ancient Wellness Tips and Practices

ancient wellness

  • A number of ancient wellness practices are now being embraced and promoted, many of which are rooted in the European wellness tradition

  • Spain has a long history of taking a siesta during the hottest time of the afternoon. The research on napping is mixed, however, with some studies showing benefits while others have come to the opposite conclusion

  • Mud treatments and mud wraps, which have been used therapeutically for 25 centuries, were popularized by the Italians during the Roman Empire. Mud therapy is often referred to as fangotherapy, after the Italian word “fango,” which means “mud”

  • Contrast therapy — a popular tradition in Finland — typically involves the use of sauna followed by cold-water immersion, either in a lake, pool, shower or bath. In the winter, immersing yourself in snow is another option

  • Other trending wellness practices include the Nordic diet, forest bathing and uitwaaien, a Dutch word referring to spending time outdoors in wild and windy weather

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As holistic health gains hold, a number of ancient wellness practices are being embraced and promoted. According to a March 2, 2020, article1 in The Guardian, many of these practices are rooted in the European wellness culture. Following is a sampling of ancient holistic health traditions making a comeback. How many of them have you tried?

Spain has a long history of taking a siesta during the hottest time of the afternoon. To this day, many Spaniards will take a break from work in the afternoon and work later into the evening to compensate. The Guardian quotes Paul Joseph, founder of Health and Fitness Travel:2

“Even just slowing down for a short period of time allows you to disconnect from the world and subsequently boost energy, focus and creativity.”

The research on napping is mixed, however, with some studies showing benefits such as lowering the prevalence of heart disease (particularly among working men),3 improving learning,4 boosting emotional stability and lowering blood pressure, while others show it may actually increase the risk of high blood pressure, diabetes and cognitive decline, especially in older adults.5

While it’s unlikely that naps are directly causing these health problems, the association exists nonetheless, and more research is needed to determine who benefits from naps, who doesn’t and why.

Mud treatments and mud wraps, which have been used therapeutically for 25 centuries,6 were popularized by the Italians during the Roman Empire. Mud therapy is often referred to as fangotherapy, after the Italian word “fango,” which means “mud.”

Mud is generally advertised as having cleansing and relaxing, antistress effects, but science suggests its health benefits may be far-reaching. As reported in the Spanish journal Anales de Medicina Interna:7

“Mud has a place as a non-pharmacological tool in certain clinical settings, such as degenerative articular processes, skin disorders, and others … Fangotherapy in arthritis patients seems to cause variations in amino acid involved in cartilage homeostasis, and also produce reduction in pain ratings in gonarthrosis.

Mud modifies nitric oxide, myeloperoxidase and glutathione peroxidase serum levels in arthritic patients and beta-endorphin and stress hormones in patients affected by osteoarthritis by reducing inflammation, pain and therefore diminishes the cause of stress.

[It] has been confirmed that the thermal stress associated with Fangotherapy activates the pituitary gland … Furthermore, steroids and antimicrobial activity of certain therapeutic mud has been suggested.”

Contrast therapy typically involves the use of sauna followed by cold-water immersion, either in a lake, pool, shower or bath. In the winter, immersing yourself in snow is another option. Sauna bathing has a long history in Finland.

To this day, most homes in Finland have a built-in sauna. Sauna bathing has been shown to strengthen heart health and offer significant protection against cardiovascular diseases,8 and adding the contrast of a cold dip afterward can further magnify those effects.

Sauna bathing is one of my favorite therapies as it generates heat shock proteins that repair protein misfolding, which is a major part of aging and disease. I believe this is why all-cause mortality is so radically decreased in Finns who sauna more than five times a week.

Sweating in a sauna will also help eliminate toxins, improve blood circulation, kill disease-causing microbes and improve your mitochondrial function. Research has even shown that regular sauna use correlates with a reduced risk of death from any cause, and may help stave off Alzheimer’s disease and dementia.

For example, researchers in Finland found that men who used a sauna four to seven times a week for an average of 15 minutes had a 66% lower risk of developing dementia, and 65% lower risk of Alzheimer’s, compared to men who used the sauna just once a week.910

Recent research11 has also demonstrated that sauna bathing helps modulate your autonomic nervous system, which governs your stress responses.12 This helps explain why most people feel “nice and mellow” afterward.

There is a compelling body of evidence showing exposure to harsh conditions can be highly beneficial and that extreme temperature variations help optimize many biological functions. Like exposure to heat, exposure to cold boosts mitochondrial function and numbers. Cold thermogenesis has also been shown to:131415

  • Strengthen joint tissue and improve

  • Support weight loss efforts by increasing metabolism

  • Increase blood circulation

  • Reduce symptoms of depression and anxiety by at least 50%16

  • Speed rate of recovery following joint or muscle injury17

  • Provide temporary relief lasting about 90 minutes from pain associated with arthritis18

  • Reduce pain and swelling following injury

  • Reduce your risk of developing cognitive decline and dementia by reducing inflammation and oxidative stress19

  • Reduce inflammation

  • Improve symptoms of eczema20

  • Enhance benefits of physical therapy

  • Reduce pain associated with migraines when applied to the back of the neck for about 30 minutes21

  • Improve muscle function and strength

  • Boost mental focus and attention by increasing production of norepinephrine in your brain.

  • Norepinephrine can be increased twofold just by getting into 40-degree F. water for 20 seconds, or 57-degree water for a few minutes

Forest bathing is the English translation of the Japanese term “shinrin-yoku.” As the term suggests, it refers to the restorative and “cleansing” effects of spending time in forests and other nature spaces. In Japan, it’s a revered and long-standing tradition known to promote health and well-being.

The benefits of forest bathing go beyond the obvious. As explained in the film, “Call of the Forest,” trees have medicinal properties.22 For example, limonene, produced by trees, is an anticancer compound used in chemotherapy.

Linolenic acids aid brain functioning and pinenes have antibiotic properties. Inhaling these and other compounds emitted by trees can provide a mildly narcotic effect while boosting immune function and relaxing your body. The soil of the forest also has healing powers, including soil bacteria shown to improve mood, so don’t be afraid to get your hands dirty.

The Dutch word “uitwaaien” is a similar term, but refers more specifically to spending time outdoors in “wild, windy weather.” According to The Guardian:23

“By replacing ‘bad air’ with ‘good air,’ it is believed to leave you feeling clear-headed and refreshed. ‘It feels exhilarating — wind is distracting, so it’s sort of meditative, in the sense you cannot think about anything else,’ says [Global Wellness Institute research director, Beth] McGroarty.”

Without doubt, spending more time in nature is one of the simplest ways to improve your general well-being and emotional health.

A massive study24 involving data from more than 140 trials and 290 million people revealed exposure to greenspace — defined as open, undeveloped land with natural vegetation — led to significant reductions in diastolic blood pressure, salivary cortisol (a physiological marker of stress) and heart rate, along with significant decreases in Type 2 diabetes and mortality from all causes and those specifically related to the heart.

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Disclaimer: The entire contents of this website are based upon the opinions of Dr. Mercola, unless otherwise noted. Individual articles are based upon the opinions of the respective author, who retains copyright as marked.

The information on this website is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended as a sharing of knowledge and information from the research and experience of Dr. Mercola and his community. Dr. Mercola encourages you to make your own health care decisions based upon your research and in partnership with a qualified health care professional. The subscription fee being requested is for access to the articles and information posted on this site, and is not being paid for any individual medical advice.

If you are pregnant, nursing, taking medication, or have a medical condition, consult your health care professional before using products based on this content.

WHO Releases Guide to ‘Combating Misinformation’

  • The World Health Organization announced that it’s working with Big Tech to combat misinformation online

  • As a result of WHO’s “policy updates,” 850,000 YouTube videos related to “harmful or misleading COVID-19 misinformation” were removed from the platform from February 2020 to January 2021

  • Lest you see all sides of an issue and form an educated opinion of your own, WHO intends to carefully control the internet so you only see what it deems as the “truth”

  • To accomplish this, WHO is working closely with master manipulators in their own right, including YouTube, Google, Facebook and NewsGuard

  • WHO has dedicated a webpage to reporting misinformation online, with direct links to social media platforms, making it easy to snitch on those who go against the status quo

  • Significant portions of regulatory agencies’ budgets around the globe come from the pharmaceutical industry that these agencies are supposed to regulate

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You can sleep easy tonight. The World Health Organization announced that it’s working with Big Tech to combat misinformation online. It didn’t define what “misinformation” it’s targeting, or even what “misinformation” is, but if you see anything that looks suspicious, WHO wants you to report it right away so social media platforms can flag it or take it down.1

Sound disturbing? More like a nightmare, but it’s one that is, unfortunately, not a dream. As John Campbell, a retired nurse and teacher based in England, said in the video above, “It’s almost as if they want to have an influence over all parts of social media.”2 Yes, indeed, and they’re quite open about it too. WHO states that it’s “changing social media policy and guidelines,” and:3

“WHO works with social media policy departments to ensure company policy and guidelines for content providers are fit for purpose. For example, WHO worked with YouTube to enhance their COVID-19 Misinformation Policy and provide guidelines for content providers to ensure no medical misinformation related to the virus proliferates on their platform.”

As a result of WHO’s “policy updates,” 850,000 YouTube videos related to “harmful or misleading COVID-19 misinformation” were removed from the platform from February 2020 to January 2021.4 As justification for its rampant censorship, WHO explains:5

“WHO and partners recognize that misinformation online has the potential to travel further, faster and sometimes deeper than the truth — on some social media platforms, falsehoods are 70% more likely to get shared than accurate news. To counter this, WHO has taken a number of actions with tech companies to remain one step ahead.”

Lest you see all sides of an issue and form an educated opinion of your own, WHO intends to carefully control the internet so you only see what it deems as the “truth.” And it’s working closely, “on a weekly basis,” in fact, with master manipulators in their own right, including YouTube, Google, Facebook and “several other partners such as NewsGuard …”6

Ah yes, NewsGuard, another self-appointed internet watchdog that sells a browser plugin to rate websites on nine criteria of credibility and transparency. NewsGuard received much of its startup funds from Publicis Groupe, a giant global communications group with divisions that brand imaging, design of digital business platforms, media relations and health care.

Publicis Groupe’s health subsidiary, Publicis Health, names Lilly, Abbot, Roche, Amgen, Genentech, Celgene, Gilead, Biogen, Astra Zeneca, Sanofi, Bayer and other Big Pharma giants as clients. In fact, the PR firm that created and ran Purdue Pharma’s deceptive marketing campaigns for the opioid Oxycontin is none other than Publicis.

At the beginning of May 2021, the Massachusetts attorney general filed a lawsuit7 against Publicis Health, accusing the Publicis subsidiary of helping Purdue create the deceptive marketing materials used to mislead doctors into prescribing OxyContin. We’re going down a rabbit hole, but you know you can tell a lot about an organization by who its friends are.

WHO is also enlisting the help of basically anyone who will listen and fall for their blatant propaganda to report “misinformation” about COVID-19 and COVID-19 shots that goes against its policies. According to WHO:8

“Social media platforms have … granted WHO access to fast track reporting systems, which allows us to flag misinformation on their platforms, speeding up the reporting and removal of content that breaks policy. WHO also works with Member States such as the Government of the United Kingdom to raise awareness of misinformation around COVID-19 and vaccines, and encourage individuals to report false or misleading content online.”

Conveniently, WHO has taken the guesswork out of how to report said misinformation. They’ve dedicated a webpage to reporting misinformation online, with direct links to the following social media platforms, making it easy to snitch on those who go against the status quo:9

  • Facebook

  • YouTube

  • Twitter

  • Instagram

  • WhatsApp

  • TikTok

  • LinkedIn

  • Viber

  • VK

  • Kwai

WHO won’t stop at controlling the internet. It’s also aiming to “save the world” from infectious diseases, food system failures and more by creating a globalist organization with synchronized plans — and the potential for ultimate control and power.

This was revealed in October 2022, when WHO announced a new initiative called One Health Joint Plan of Action. The plan was launched by the Quadripartite which, in addition to WHO, consists of the:10

  • Food and Agriculture Organization of the United Nations (FAO)

  • United Nations Environment Programme (UNEP)

  • World Organisation for Animal Health (WOAH, founded as OIE)

WHO already has too much power. This new initiative will only give it more. It’s important to understand that Bill Gates is WHO’s No. 1 funder, contributing more to WHO’s $4.84 billion biennial budget11 — via multiple avenues including the Bill & Melinda Gates Foundation as well as GAVI, which was founded by the Gates Foundation in partnership with WHO, the World Bank and various vaccine manufacturers — than any member-state government. In short, Bill Gates is essentially the owner of WHO.

In 1992, the Prescription Drug User Fee Act (PDUFA) was created, which allows the U.S. Food and Drug Administration to collect fees from the drug industry. “With the act, the FDA moved from a fully taxpayer-funded entity to one supplemented by industry money,” a BMJ article written by investigative journalist Maryanne Demasi explains.12

Now, significant portions of regulatory agencies’ budgets come from the pharmaceutical industry that these agencies are supposed to regulate. In 1993, after PDUFA was passed, the FDA collected about $29 million in net PDUFA fees. This increased 30-fold — to $884 million — by 2016.13

It’s also revealing, as noted by Campbell, that at the FDA, 9 out of 10 of its former commissioners between 2006 and 2019 went on to work for pharmaceutical companies.14 But it’s not only U.S. regulators who are captured by industry; a similar trend occurred in Europe. In 1995, industry fees funded 20% of the European Medicines Agency (EMA). This rose to 75% by 2010 and now, in 2022, it’s 89%. According to Demasi:15

“In 2005 in the UK, the House of Commons’ health committee evaluated the influence of the drug industry on health policy, including the Medicines and Healthcare Products Regulatory Agency (MHRA).

The committee was concerned that industry funding could lead the agency to ‘lose sight of the need to protect and promote public health above all else as it seeks to win fee income from the companies.’ But nearly two decades on, little has changed, and industry funding of drug regulators has become the international norm.”

How do regulators from different countries compare? “Industry money permeates the globe’s leading regulators,” Demasi wrote, demonstrated as follows:16

  • Australia’s Therapeutic Goods Administration — 96% of budget derived from industry

  • Europe’s EMA — 89%

  • U.K.’s MHRA — 86%

  • Japan’s Pharmaceuticals and Medical Devices Agency — 85%

  • U.S. FDA — 65%

  • Health Canada — 50.5%

“Are these the official bodies that we want to adjudicate over what health information we are given, over which drugs are good for us and which drugs are bad for us?” Campbell said. “Is this really who we want to make these decisions, given the amount of funding they’re receiving from, what some people might consider to be, vested interests?”17

“We’re talking about large amounts of money, which have no influence on decision-making,” he says sarcastically. “And yet these official agencies are going to decide what health information you and I are going to receive.”18

Access to information as it once was has been fundamentally changed. WHO and other world leaders are now working together to silence information that doesn’t correspond with its common agenda. Even information that was once fact, such as definitions in dictionaries and on official government websites, have been altered in real time.

Examples of definitions that have been changed include those for pandemic, herd immunity, vaccines and anti-vaxxer. Investigative journalist Sharyl Attkisson is among those who have explained that virtually everything you see and hear online has been coopted, or taken over to serve a greater agenda. Attkisson reiterates:19

“Virtually every form of information and sourcing that can be coopted has been. That includes the dictionary definitions, that includes everything because these are important ways to influence thought. Language is very powerful. People don’t want to be affiliated with certain names and labels.

It reminds me of 1984, the George Orwell story about the futuristic society, under which history was being rewritten in real time to jive with the version that the government wanted or the party wanted it to be. Definitions now are being rewritten and changed in real time to fit with the vision that the establishment wants people to think.”

Campbell also quotes “1984,” which stated, “It was expected that Newspeak would have finally superseded Oldspeak (or Standard English, as we should call it) by about the year 2050.”20 “Let’s hope it doesn’t get there before that,” Campbell said. “I kind of like Oldspeak. It’s the one I was brought up with.”

Orwell wrote, “The purpose of Newspeak was not only to provide a medium of expression for the world-view and mental habits proper to the devotees of Ingsoc [the ruling party], but to make all other modes of thought impossible.”21

“The C vocabulary [a component of Newspeak] was supplementary to the others and consisted entirely of scientific and technical terms. These resembled the scientific terms in use today, and were constructed from the same roots, but the usual care was taken to define them rigidly and strip them of undesirable meanings.”22

And then there are the three slogans, “War is peace, freedom is slavery, ignorance is strength,” which are contradictory yet widely accepted by the people. It’s food for thought, as WHO and other regulatory agencies become increasingly blatant in their censorship and suppression of freedom. “Make of that what you will,” Campbell says.

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Disclaimer: The entire contents of this website are based upon the opinions of Dr. Mercola, unless otherwise noted. Individual articles are based upon the opinions of the respective author, who retains copyright as marked.

The information on this website is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended as a sharing of knowledge and information from the research and experience of Dr. Mercola and his community. Dr. Mercola encourages you to make your own health care decisions based upon your research and in partnership with a qualified health care professional. The subscription fee being requested is for access to the articles and information posted on this site, and is not being paid for any individual medical advice.

If you are pregnant, nursing, taking medication, or have a medical condition, consult your health care professional before using products based on this content.

Will Elon Musk Turn Twitter’s Tide Against Censorship?

elon musk twitter censorship

  • Within weeks of Elon Musk taking over Twitter, information gatekeepers and controllers are panicking about rising engagement on posts from people accused of spreading misinformation

  • According to NewsGuard, the Mercola Twitter account saw the largest increase in likes and retweets out of those that have previously been most heavily censored

  • Two weeks before Musk’s takeover, we had 932 engagements in a seven-day period. During the first week after Musk’s takeover, we had 19,259 engagements, a 1,966.4% increase, which NewsGuard claims is proof that dangerous falsehoods are again proliferating

  • Even if Twitter allows free speech, censorship stakeholders span every major media conglomerate, online payment provider, college and university, hundreds of think tanks, NGOs, international regulators and watchdog groups. Censorship is also the policy of the U.S. State Department, the Pentagon and the intelligence services

  • What we face is a corporate stronghold over media combined with a state-run propaganda machine. Countless private-public partnerships between government and corporations bind the two camps together in a pact to dictate “truth” to the public, and they’re on the same page, because their interests are identical. The goal is a One World Government

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With Elon Musk now behind the wheel at Twitter, will the platform become a safe haven for free speech? Time will tell, but for now, things seem to be moving in the right direction. Of course, information gatekeepers and controllers are already going into convulsions over the fact that engagement on posts from sites like mine have gone up from near-nonexistent to negligible.

November 11, 2022, self-proclaimed arbiter of truth, NewsGuard, wrote:1

“In the week following Elon Musk’s acquisition of Twitter, the most popular untrustworthy accounts enjoyed a 57.04% increase in engagement in the form of likes and retweets, according to a survey undertaken by NewsGuard …

In the week after the acquisition (Oct. 27, 2022-Nov. 3, 2022), tweets posted by the 25 most-followed Twitter accounts that are tracked by NewsWhip, a social media monitoring company, and linked to publishers that NewsGuard has assessed as repeatedly spreading false information garnered 3,115,664 likes and retweets …

Two weeks prior to the acquisition, Oct. 13-Oct. 20, 2022, those same accounts received 1,983,953 likes and retweets. (Likes and retweets constitute overall ‘engagement.’) That accounts for a 57.04% cumulative increase post-Musk. (Note: These 25 accounts are in the top-50 most followed NewsGuard-rated untrustworthy accounts …)

For example, the interactions of the Twitter account linked to Mercola.com — a website of healthcare hoax purveyor Joseph Mercola that has published numerous false claims about vaccines and the COVID-19 pandemic — rose from 932 to 19,259, a 1966.42% increase in engagement and the largest increase measured by NewsGuard. At the same time, the account’s tweet volume rose from 6 to 23.”

Oh boy, a rise in engagement from 932 likes and retweets to 19,259! Nineteen thousand people engaged with my articles, and the roof is caving in on propaganda headquarters. That’s how fragile their house of cards is. To be clear, 19,000 engagements in a week are nothing compared to the reach and engagements we used to have.

Even more ridiculous is NewsGuard’s panic over the “explosion” of exposure of Dr. Christiane Northrup, whose weekly engagement tally rose from 63 to 704 after Musk’s entry into the wheelhouse. Just incredible. How are they ever going to keep the brainwashing going when 700 people are exposed to the likes of Northrup?! In a single week!

Sarcasm aside, this just goes to show how desperate the propagandists are. To top off their indignation, Musk has not replied to the emails and calls made by NewsGuard in November “asking about its handling of untrustworthy accounts and the boost in engagement for misinformation spreaders.” The nerve.

That said, some analysts predict Musk’s Twitter takeover will have little effect on censorship, on or off Twitter. Writing for Townhall in early May 2022, columnist Mike Benz noted:2

“As a former State Department diplomat in charge of the ‘Big Tech’ portfolio, I have had a privileged glimpse into the myriad forces driving modern Internet censorship.

Having seen what Musk is up against first-hand, I feel little elation at the arrival of the Deus Ex Muskina. From 2006 to 2016, censorship was an act. In the five years that followed, censorship became an industry.

Its powerful stakeholders now span every major media conglomerate, every major online payment provider, every major US and UK college and university, hundreds of think tanks, NGOs and pressure groups, international regulatory and watchdog commissions, and is now firmly interwoven with the policies and operations of the US State Department, the Pentagon, and the intelligence services …

Last week [end of April 2022], tech investor and Facebook board member Marc Andreesen tweeted that online censorship will become increasingly standardized, moving ‘up the stack’ into cloud platforms, email clients, browsers, and operating systems.

It’s already happening. Just this week, Google embedded AI censorship into its Google Docs word processor to add friction for users engaged in wrongspeak.

Microsoft already changed its Windows terms of service in 2019 to ban PC users engaged in undefined ‘hate speech’ … Inevitably, the censorship industry will promote rule-of-law pretexts to force Musk to crush a free speech Twitter.”

In addition to those listed by Benz, additional censorship stakeholders and promoters are detailed in “The Web of Players Trying to Silence Truth.” A key hub within this vast network are PR firms that represent the corporatocracy (the economic, political and judicial systems controlled by corporations).

The role of the free press is to counter industry propaganda. Over time, that role was subverted through advertising. This is why news outlets rarely, if ever, touch on anything that might damage their advertisers.

In addition to that already powerful incentive to censor the truth, there’s the fact that the U.S. government legalized the use of state propaganda against American citizens in 2012.

So, what we face now is a corporate stronghold over media combined with a state-run propaganda machine. Countless private-public partnerships between government and corporations bind the two camps together in a pact to dictate “truth” to the public, and they’re on the same page, because their interests are identical.

The goal is to sacrifice United States’ sovereignty to a One World Government, using the need for global biosecurity and the impending threat of climate change as justifications for doing so.

To that end, we have centralized propaganda hubs like the Publicis Groupe, one of the largest PR firms in the world, which represents a long list of major companies within the technology, pharmaceutical and banking industries AND is a partner of the World Economic Forum (WEF) and Google,3 4 AND funded the startup of NewsGuard.

Those connections alone give Publicis the ability to direct and control censorship through fact checkers and online search engines.

NewsGuard, in turn, is partnered with the U.S. State Department, the U.S. Department of Defense, the World Health Organization5 and the Centre for Countering Digital Hate (CCDH) — a dark money group with extensive ties to government and global think tanks that is calling for the weaponization of intelligence and national defense against citizens who see through the propaganda.

The WEF, meanwhile, is leading the call for a “reset” of the global economy and a complete overhaul of our way of life, and its partner Publicis appears to play an important role, coordinating the suppression of information that runs counter to the WEF’s technocratic, transhumanist narrative.

Incidentally, Publicis began investing in artificial intelligence technology in 20176 and partnered with Microsoft in 2018 to develop a global AI platform.7 It also purchased the data firm Epsilon in 2019,8 thereby establishing ownership of first-party data — a crucially valuable resource when it comes to the use of AI. Of course, AI is an indispensable tool in the digital surveillance and control structure the globalist cabal is trying to erect.

While it’s easy to dismiss Publicis as just another ad agency, I believe it would be foolish to underestimate its power to organize the kind of coordination required to shut down vaccine concerns, anti-lockdown proponents and people trying to educate their fellow man about the dangers of The Great Reset, which is being brought forth as a “necessary” post-COVID step.

While these things may seem unrelated, they’re really not. The Great Reset involves all aspects of society — including health, education, government, economics, business practices, environmental “protections” and much more.

With forces this formidable against us, is it even possible to rein in the tyranny, push back the censorship and reclaim our rights? I don’t know, but we have to try, and using what power remains within the judicial system is the first option.

So, in late 2021, I filed a lawsuit against U.S. Sen. Elizabeth Warren, both in her official and personal capacities, for violating my First Amendment rights. In early September 2021, she had sent a letter9 to Andy Jassy, chief executive officer of Amazon.com, demanding an “immediate review” of Amazon’s algorithms to weed out books peddling “COVID misinformation,” stressing that Amazon’s sale of such books was “potentially unlawful.”10 11 12

She specifically singled out my book, “The Truth About COVID-19,” co-written with Ronnie Cummins, founder and director of the Organic Consumers Association (OCA), as a prime example of “highly-ranked and favorably-tagged books based on falsehoods about COVID-19 vaccines and cures” that she wanted banned.

There’s no doubt our book is constitutionally protected speech, and that Warren’s letter was calling on Amazon to suppress protected speech. As a government official, it is illegal for Warren to violate the U.S. Constitution, and pressuring private businesses to do it for her is not a legal workaround.

Then, in September 2022, I sued YouTube, Google and Alphabet Inc. for breach of contract. September 29, 2021, Google deleted my YouTube account for “violating community guidelines” they’d implemented that same morning. YouTube unilaterally amended the contract without notice, which is a violation of its own terms, and then used this last-minute amendment to remove my content.

YouTube’s terms of service also include a “three strikes” policy, where users are supposed to be given three warnings and opportunities to remove content that violates the guidelines before being banned. I had no “strikes” against my channel on the day I was deplatformed and deleted, which is, again, a breach of contract.

I’m also suing YouTube for unjust enrichment, as for the last 16 years, my video content, having generated in excess of 50 million views, has been of great financial benefit to YouTube, allowing them to increase advertising revenue on the site. Both of these lawsuits are still winding their way through the corridors of justice.

Others have also taken the fight to court. The New Civil Liberties Alliance and the attorneys general of Missouri and Louisiana (Eric Schmitt and Jeff Landry) sued the federal government in May 202213 for violating Americans First Amendment rights by colluding with social media companies to censor on the government’s behalf.

In early October 2022, 47 additional defendants were added to the lawsuit, bringing the total number of named defendants to 67.14 15 As reported by the New Civil Liberties Alliance September 1, 2022:16

“… scores of federal officials … have secretly communicated with social-media platforms to censor and suppress private speech federal officials disfavor. This unlawful enterprise has been wildly successful.

Under the First Amendment, the federal government may not police private speech nor pick winners and losers in the marketplace of ideas. But that is precisely what the government has done — and is still doing — on a massive scale not previously divulged.”

Discovery documents obtained have identified upward of 70 federal employees across more than a dozen federal agencies, engaged in illegal censorship activities, including officials from:

  • The Cybersecurity and Infrastructure Security Agency’s (CISA) Election Security and Resilience team

  • Department of Homeland Security’s (DHS) Office of Intelligence and Analysis

  • The FBI’s foreign influence taskforce

  • The Justice Department’s (DOJ) national security division

  • The Office of the Director of National Intelligence

  • White House staff (including White House lawyer Dana Remus, deputy assistant to the president Rob Flaherty and former White House senior COVID-19 adviser Andy Slavitt)

  • Health and Human Services (HHS)

  • Centers for Disease Control and Prevention (CDC)

  • National Institutes of Allergy and Infectious Diseases (NIAID)

  • The Office of the Surgeon General

  • The Census Bureau

  • The Food and Drug Administration (FDA)

  • The State Department

  • The U.S. Treasury Department

  • The U.S. Election Assistance Commission

Emails from the strategic communications and marketing firm Reingold17 also reveal outside consultants were hired to manage the government’s collusion with social media to violate Americans’ Constitutional free speech rights.

Notable tech participants in the censorship meetings include Google, Facebook, Twitter, YouTube, Reddit, Microsoft, Verizon Media, Pinterest, LinkedIn and the Wikimedia Foundation.

Not surprisingly, the White House has not cooperated with discovery and have fought to keep communications secret — especially with regard to Dr. Anthony Fauci’s correspondence — claiming all White House communications as “privileged.”

However, executive privilege does not apply to external communications, so the plaintiffs called on the U.S. District Court for the Western District of Louisiana to “overrule the government defendants’ objections and order them to supply this highly relevant, responsive and probative information immediately.”

September 6, 2022, Judge Terry Doughty rejected the Biden administration’s claim of executive privilege and ordered the White House to hand over any and all relevant records,18 19 including correspondence to and from Fauci, White House press secretary Karine Jean-Pierre and many others.

October 21, 2022, the court also authorized20 expedited depositions of eight key federal officials named in the AGs case: Fauci, former White House press secretary Jen Psaki, director of White House digital strategy Rob Flaherty, Surgeon General Vivek Murthy, CISA director Jen Easterly, FBI supervisory special agent Elvis Chan, chief of the digital media branch of the CDC Carol Crawford, and principal deputy coordinator of the Global Engagement Center at the State Department Daniel Kimmage.21 22

The DOJ, clearly worried about the fallout, asked the judge for a protective order to keep videotaped depositions under seal. With that, the DOJ has tipped its hand, proving it is onboard with these unconstitutional activities. As of this writing, there’s no word as to whether the judge will grant the DOJ’s request to keep the depositions secret.

“This case has garnered substantial attention from the media and the public,” the DOJ wrote.23 “Some of the individuals whom Plaintiffs intend to depose are career civil servants who did not sign up to become public figures when they joined the federal ranks.

Other deponents who have served in more public-facing roles have already experienced, and continue to experience, significant threats and harassment directed at them and their families because of their public positions; those harms are very likely to increase if recordings of their depositions may be publicly circulated and then misleadingly edited by third parties.

Under these circumstances, all these individuals have legitimate privacy interests in limiting public dissemination of audiovisual recordings of their depositions.”

While the U.S. Constitution guarantees certain rights, including the right to free speech, this inviolable law of the land has not been able to prevent encroaching tyranny, thanks to the fact that those charged with adhering to it and upholding it aren’t doing their jobs. They’re blatantly snubbing their noses at it, pretending as though it doesn’t exist.

In response, three Republican House Representatives on the House Oversight and Reform, Judiciary, and Commerce committees — Reps. James Comer of Kentucky, Jim Jordan of Ohio, and Cathy McMorris Rodgers of Washington — have introduced the Protecting Speech from Government Interference Act24 (HR.8752), specifically aimed at preventing federal employees from using their positions to influence censorship decisions by tech platforms.

“While the U.S. Constitution clearly forbids government censoring and restricting free speech, HR. 8752 could be a helpful enforcement tool, as people might tend to think twice when they know there’s a real price to pay.”

The bill would create restrictions to prevent federal employees from asking or encouraging private entities to censor private speech or otherwise discourage free speech, and impose penalties, including civil fines and disciplinary actions for government employees who facilitate social media censorship.

While the U.S. Constitution clearly forbids government censoring and restricting free speech, HR. 8752 could be a helpful enforcement tool — and we clearly need enforcement — as people might tend to think twice when they know there’s a price to pay, both personally and financially.

The Great Reset is moving full speed ahead, and those who disagree are being silenced for the simple reason that if people knew what was in store, the plan would get thwarted. They need the cooperation of the masses, or else it won’t work.

The answer, then, is to continue exposing the machinations that allow this agenda to be pushed forward. Understand, each and every one of us has an important role to play in this process. We must expose their plans, goals, networks and battle strategies, and we do that by sharing what we know in whatever capacity we can, be it through social media posts, emails, texts, phone calls, face-to-face encounters, groups, clubs or at church.

Share articles such as this one with everyone you know so that people can start to understand how and why they are being manipulated. This will effectively “immunize” them against the propaganda.

Secondly, encourage your friends and family to subscribe to this and other newsletters to keep abreast on the next steps that will be necessary to defeat the tyrants who are hell-bent on global control. Right now, that would include calling on your representatives to back HR. 8752.

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Disclaimer: The entire contents of this website are based upon the opinions of Dr. Mercola, unless otherwise noted. Individual articles are based upon the opinions of the respective author, who retains copyright as marked.

The information on this website is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended as a sharing of knowledge and information from the research and experience of Dr. Mercola and his community. Dr. Mercola encourages you to make your own health care decisions based upon your research and in partnership with a qualified health care professional. The subscription fee being requested is for access to the articles and information posted on this site, and is not being paid for any individual medical advice.

If you are pregnant, nursing, taking medication, or have a medical condition, consult your health care professional before using products based on this content.

The Importance of Muscle in Healthy Aging

  • The older you get, the more important your muscle mass becomes. Not only are strong muscles a requirement for mobility, balance and the ability to live independently, but having reserve muscle mass will also increase your chances of survival during illness and hospitalization

  • Age-related loss of muscle mass is known as sarcopenia, and if you don’t do anything to stop it you can expect to lose about 15% of your muscle mass between your 30s and your 80s

  • While declines in muscle mass and strength are relatively well-synchronized in the 35- to 40-year-old group, strength dramatically drops off as you get into the 75-year-old and over groups, with 85-year-olds seeing dramatic declines in strength and function relative to the decline in muscles size

  • Research shows the strongest one-third of the population over 60 have a 50% lower death rate than the weakest

  • Research shows aerobic exercise in isolation reduces your all-cause mortality by 16% and strength training-only reduces it by 21%, whereas if you do both, you reduce your all-cause mortality by 29%

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The older you get, the more important your muscle mass becomes. Not only are strong muscles a requirement for mobility, balance and the ability to live independently, but having reserve muscle mass will also increase your chances of survival1 when sick or hospitalized.

Muscle is lost far more easily and quicker than it’s built, so finding ways to continuously promote and maintain your muscle mass is really crucial, especially as you get older.

Age-related loss of muscle mass is known as sarcopenia, and if you don’t do anything to stop it you can expect to lose about 15% of your muscle mass between your 30s and your 80s.2 An estimated 10% to 25% of seniors under the age of 70 have sarcopenia and as many as half those over the age of 80 are impaired with it.3

In the lecture above, Brendan Egan, Ph.D., associate professor of sport and exercise physiology at the School of Health and Human Performance and the National Institute for Cellular Biotechnology at Dublin City University in Ireland, reviews the latest research on exercise training for aging adults, which places a significant focus on building and maintaining muscle, and the nutritional components that can help optimize training results.

While it’s true that larger muscle is indicative of stronger, more functional muscle, it’s not a true 1-to-1 relationship. As noted by Egan, “you can have situations where you can gain back function without necessarily gaining muscle size.” To illustrate this point, Egan presents data from the Baltimore Longitudinal Study of Aging, which looked at leg strength and lean muscle mass.

While declines in muscle mass and strength are relatively well-synchronized in the 35- to 40-year-old group, strength dramatically drops off as you get into the 75-year-old and over groups, with 85-year-olds seeing dramatic declines in strength and function relative to the decline in muscles size.

One way to measure functional capacity in older adults is gait (walking) speed, which is a strong predictor of life expectancy. Data suggest that if you have a walking speed of 1.6 meters (about 5.2 feet) per second (approximately 3.5 mph) at the age of 65, your life expectancy is another 32 years, meaning you may live into your late 90s.

Having a walking speed at or below the cutoff for sarcopenia, which is 0.8 meters (about 2.6 feet) per second, your life expectancy would be another 15 years, which means you’d be predicted to live to 80. At this speed, you would not be able to make it safely across a typical pedestrian crossing before the light changes to red.

Strength can also tell us a lot about an individual’s chances of survival. Egan presents data from a study in which people’s chest and leg press strength were measured to arrive at a composite score of whole body strength. The pattern is quite revealing, showing the strongest one-third of the population over 60 had a 50% lower death rate than the weakest.

Exercise guidelines recommend getting 150 minutes of aerobics exercise and two strength training sessions per week. As noted by Egan, you need both. It’s not just one or the other.

Research shows aerobic exercise in isolation reduces your all-cause mortality by 16% and strength training-only reduces it by 21%, whereas if you do both, you reduce your all-cause mortality by 29%.4 Disturbingly, U.K. data suggest only 36.2% of adults over the age of 30 meet aerobic guidelines, and a minuscule 3.4% meet strength training guidelines.

Part of the problem may be that many don’t want to go to the gym. But there’s little difference between doing gym-based strength training and doing bodyweight resistance training at home.

As noted by Egan, enforced bedrest, such as acute hospitalization, can have a dramatic impact on your muscle mass. For example, a 2015 review5 in Extreme Physiology & Medicine notes you can lose 2.5% of your muscle mass in the first two weeks of bedrest. By Day 23, you can have lost up to 10% of your quadriceps muscle mass. As explained in this review:6

“Skeletal muscle mass is regulated by a balance between MPS [muscle protein synthesis] and MPB [muscle protein breakdown]. In a 70-kg human, approximately 280 g of protein is synthesized and degraded each day.

The two processes are linked … as facilitative or adaptive processes, whereby MPS facilitates (allows modulation of muscle mass) and MPB adapts (limiting said modulation).

When exposed to an anabolic stimulus, MPS rises. MPB rises too, but to a lesser amount, resulting in a net synthetic balance. In response to an anti-anabolic stimulus, MPS decreases and MPB decreases to a lesser degree, resulting in a net breakdown.

The interaction between critical illness and bed rest may result in greater muscle loss compared to bed rest alone. The musculoskeletal system is a highly plastic and adaptive system, responding quickly to changing demands. Relatively short periods of immobilization decrease MPS, with no effect on MPB.

Furthermore, this altered balance is relatively resistant to high dose amino acid delivery … Immobilization has significant effects on peripheral muscle aerobic capacity, contractility, insulin resistance and architecture.

Microvascular dysfunction occurring in severe sepsis is associated with immobilization and may have an additive effect on reducing MPS. In critically ill patients, MPS is reduced even with nutritional delivery, with increased MPB seen, leading to a net catabolic state and thus muscle wasting.”

Research7 has shown even healthy young subjects in their 20s can lose 3.1 pounds of muscle mass in a single week of bedrest. This is why it is so important to have a reserve in case you wind up in the hospital and lose this much muscle mass. It may take you the better part of a year to regain that muscle, as gaining muscle mass is hard work and many elderly fail to do so.

The loss of muscle mass also significantly decreases your insulin sensitivity. One of the reasons for this has to do with the fact that muscle tissue is a significant reservoir for the disposal of glucose. Your muscle tissue also produces cytokines and anti-inflammatory myokines that play an important role in health.

While three to five sessions of aerobic exercise and two or more strength sessions per week may sound like a lot, for many, the lack of time is a restricting factor. However, some of these sessions can be done together. “That’s called concurrent exercise training,” Egan says.

He goes on to cite research looking at time matched concurrent exercise in the elderly, 65 and older, where an aerobic training group and a strength training group were compared to a group that spent half of their session doing aerobic exercise and the other half doing resistance training. All groups spent the same overall time exercising (30 minutes, three times a week for 12 weeks).

In terms of leg strength, the concurrent training group had better responses to training than aerobic or strength training alone. There was little difference in lean body mass, meaning they didn’t necessarily bulk up, but they had a 50% increase in strength nonetheless. They also lost more body fat around the trunk area. In short, concurrent training appears to give you more bang for your buck.

One of the reasons I’m so passionate about blood flow restriction (BFR) training is because it has the ability to prevent and widely treat sarcopenia like no other type of training.

There are several reasons why BFR is far superior to conventional types of resistance training in the elderly. Importantly, it allows you to use very light weights, which makes it suitable for the elderly and those who are already frail or recovering from an injury. And, since you’re using very light weights, you don’t damage the muscle and therefore don’t need to recover as long.

While most elderly cannot engage in high-intensity exercise or heavy weightlifting, even extraordinarily fit individuals in their 60s, 70s and 80s who can do conventional training will be limited in terms of the benefits they can achieve, thanks to decreased microcirculation. This is because your microcirculation tends to decrease with age.

With age, your capillary growth diminishes, and capillary blood flow is essential to supply blood to your muscle stem cells, specifically the fast twitch Type II muscle fiber stem cells. If they don’t have enough blood flow — even though they’re getting the signal from the conventional strength training — they’re not going to grow and you’re not going to get muscle hypertrophy and strength.

BFR, because of the local hypoxia that is created, stimulates hypoxia-inducible factor-1 alpha (HIF1a) and, secondarily, vascular endothelial growth factor (VEGF), which acts as “fertilizer” for your blood vessels. VEGF allows your stem cells to function the way they were designed to when they were younger.

What’s more, the hypoxia also triggers vascular endothelial growth factor, which enhances the capillarization of the muscle and likely the veins in the arteries as well. Building muscle and improving blood vessel function are related, which is why BFR offers such powerful stimulus for reversing sarcopenia.

In short, BFR has a systemic or crossover training effect. While you’re only restricting blood flow to your extremities, once you release the bands, the metabolic variables created by the hypoxia flow into your blood — lactate and VEGF being two of them — thereby spreading this “metabolic magic” throughout your entire system.

podcast

It should come as no surprise that there is an important synergy between nutrition and exercise. When it comes to muscle building and maintenance, amino acids, the building blocks of protein, are of particular importance.

In the podcast above, Megan Hall, scientific director at Nourish Balance Thrive delves into this topic at greater depth and reviews the current recommended daily allowances of protein compared to the optimal levels needed to support muscle mass and strength in at various life stages.8

Research9 looking at post-prandial protein handling and amino acid absorption shows 55.3% of the dietary protein of a given meal is in circulation within five hours after eating, which significantly increases muscle protein synthesis.

Research10 suggests healthy young adult men “max out the protein synthesis signal from a given meal” at a dose of 0.24 grams of protein per kilogram of total bodyweight, or 0.25 grams of protein per kilogram of lean body mass.

The current U.S.-Canadian recommended dietary protein allowance is 0.8 g/kg/d (0,36/grams/pound/day), but healthy older adults may actually require about 1.20 g/kg/d or .55 grams/pound/day. According to this study:11

“Our data suggest that healthy older men are less sensitive to low protein intakes and require a greater relative protein intake, in a single meal, than young men to maximally stimulate postprandial rates of MPS [myofibrillar protein synthesis].

These results should be considered when developing nutritional solutions to maximize MPS for the maintenance or enhancement of muscle mass with advancing age.”

Amino acids also act as signaling molecules that trigger muscle growth. Leucine is a particularly potent signaling agent, although all of the amino acids are required to actually build the muscle. The richest source of leucine (which helps regulate the turnover of protein in your muscle), by far, is whey protein. In fact, it can be difficult to obtain sufficient amounts of leucine from other sources.

The typical requirement for leucine to maintain body protein is 1 to 3 grams daily. However, to optimize its anabolic pathway, research shows you need somewhere between 8 and 16 grams of leucine per day, in divided doses.1213

To reach the 8-gram minimum, you’d have to eat nearly 15 eggs.14 Eighty grams of whey, on the other hand, will give you 8 grams of leucine.15

One of the problems with Egan is that he’s not very literate on time-restricted eating. During the question and answer portion, an audience member asks him about it and he admits he hasn’t studied it.

This is important because restricting your eating window to six to eight hours, which means you’re fasting 14 to 18 hours each day, would make it far easier for each of the meals to be over the leucine threshold. It will also activate autophagy, which is another factor essential for optimal muscle growth.

Autophagy is a self-cleaning process in which your body digests damaged cells, which in turn encourages the proliferation of new, healthy cells. The harder your workout, the more autophagy you will activate.

So, I recommend fasting for as long as you can before your morning workout, and then, shortly thereafter, have your largest meal of the day with plenty of high-quality protein, making sure you get several grams of leucine and arginine, both of which are potent mTOR stimulators.

The mTOR pathway is an important key for protein synthesis and muscle building. As explained in David Sabatini’s excellent review paper “mTOR at the Nexus of Nutrition, Growth, Ageing and Disease,” published in Nature Reviews Molecular Cell Biology:16

“Over the past two and a half decades, mapping of the mTOR signaling landscape has revealed that mTOR controls biomass accumulation and metabolism by modulating key cellular processes, including protein synthesis and autophagy.

Given the pathway’s central role in maintaining cellular and physiological homeostasis, dysregulation of mTOR signaling has been implicated in metabolic disorders, neurodegeneration, cancer and ageing.”

In summary, fasting activates autophagy, allowing your body to clean out damaged subcellular parts. Exercising while fasted maximizes autophagy even further. In fact, exercising while you are fasting for more than 14 to 18 hours likely activates as much autophagy as if you were fasting for two to three days. It does this by increasing AMPK, increasing NAD+ and inhibiting mTOR.

Refeeding with protein after your fasted workout then activates mTOR, thus shutting down autophagy and starting the rebuilding process. These two processes need to be cyclically activated to optimize your health and avoid problems.

As noted by Egan, “Hopefully I’ve convinced you that muscle health is central to active lifestyles. There’s been this increased awareness of muscle size, but I think we need to emphasize the idea about strength and function. These are the things that are easiest to change with the right type of training.”

In short, if you want to increase muscle size and strength, then there’s no getting around resistance training. It simply must be part of your exercise prescription, and concurrent training, where you’re combining aerobic and strength training in a given session is a time-efficient model.

BFR is also a particularly excellent way to ensure you’re getting effective strength training without the risks of conventional strength training using heavy weights, and is easy to combine with exercises such as walking and swimming. You simply wear the BFR bands while walking or exercising as normal.

In my February 2020 interview with Ben Greenfield, author of “Boundless: Upgrade Your Brain, Optimize Your Body & Defy Aging,” we discuss the importance of strength training and getting the appropriate amount of protein to build and maintain your muscle mass and optimize mitochondrial density and biogenesis.

In summary, Greenfield recommends a fitness program that includes the following types of exercise in order to target the main pathways involved in health and aging:

  • High-intensity interval training once a week to boost mitochondrial density and biogenesis — Brief spurts of exercise followed by longer rest periods. Greenfield recommends a 3-to-1 or 4-to-1 rest-to-work ratio.

  • Muscle endurance training two to three times a week to improve lactic acid tolerance — An example is the classic Tabata set, which has a 2-to-1 work-to-rest ratio.

  • Longer training sessions twice a week to improve your VO2 max — To target and improve your VO2 max, you’ll want your training sessions to be longer, about four to six minutes in duration with four to six minutes of recovery in between, for a 1-to-1 work-to-rest ratio.

    Examples include The New York Times’ seven-minute workout17 and bodyweight training done in a fast explosive manner or with a very light medicine ball, sandbag or kettle bells.

  • Long walk once a week to improve your stamina — Greenfield recommends taking a 1.5- to three-hourlong walk, bike ride or paddle session — anything where your body is engaged in chronic repetitive motion for a long period of time — preferably in a fasted state. Alternatively, do 20 to 30 minutes of fasted cardio followed by a cold shower.

  • Super-slow weight training once or twice a week to improve muscle strength — Alternatives include elastic band training systems and blood flow restriction (BFR) training. You can also combine BFR with super-slow training.

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Disclaimer: The entire contents of this website are based upon the opinions of Dr. Mercola, unless otherwise noted. Individual articles are based upon the opinions of the respective author, who retains copyright as marked.

The information on this website is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended as a sharing of knowledge and information from the research and experience of Dr. Mercola and his community. Dr. Mercola encourages you to make your own health care decisions based upon your research and in partnership with a qualified health care professional. The subscription fee being requested is for access to the articles and information posted on this site, and is not being paid for any individual medical advice.

If you are pregnant, nursing, taking medication, or have a medical condition, consult your health care professional before using products based on this content.

Pfizer’s Financial Supernova and the Art of Really Big Lies

  • Pfizer’s annual revenue is expected to reach $101.3 billion in 2022, thanks to its COVID jab, which doesn’t prevent infection or spread, and Paxlovid, an ineffective and dangerous COVID antiviral that causes rebound

  • Pfizer got plenty of free help from the federal government, which bullied and harassed people into getting the shots, and implemented rules that ensure hospitals and pharmacies will only prescribe certain COVID drugs, Paxlovid being one of them

  • The key to getting away with a really big lie is making it so divorced from reality that the listener will assume their own perception is flawed, and then repeating it over and over again. This strategy has been used to great effect over the past three years, resulting in a massive shift from fact-based public health orthodoxy to irrational fantasy-based dogma

  • Centralized top-down health care is far more attractive to Big Pharma investors than patient-centered care. The primary obstacle to the corporatization and monetization of public health has been truth, and this obstacle was finally overcome during the COVID pandemic

  • The Big Lies told during the pandemic work because they veer so sharply from the truth. This break from factual reality is what makes it so difficult to question them, because if you do, you’re now questioning the entire hierarchy of public health

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The manufactured COVID pandemic has been a proverbial golden egg-laying goose for Pfizer. Its annual revenue is expected to reach $101.3 billion in 2022,1 thanks to its COVID jab, which doesn’t prevent infection or spread, and Paxlovid, an ineffective and dangerous COVID antiviral that causes rebound. It would be comical if it weren’t so egregious.

And, Pfizer’s coffers are more or less guaranteed to continue being filled to the brim as the U.S. Centers for Disease Control and Prevention’s Advisory Committee on Immunization Practices (ACIP) has now added COVID-19 shots to the U.S. childhood, adolescent and adult vaccine schedules.2

With this action, the CDC has secured Pfizer’s (and Moderna’s) permanent liability shield so that no one can sue them for damages for injuries and deaths occurring as a result of the shots. It also opens the door for states to mandate the jab for school children, which guarantees a continuous revenue stream.

That revenue stream may even exceed previous profits, as Pfizer raised the price on its COVID jab by about 400%,3 from $304 per jab to somewhere between $110 and $130, on the same day ACIP voted to add the shot to the vaccine schedule. That price hike will take effect once the current U.S. purchase program expires.

As reported by Kaiser Health News (KHN),5 “a fortune amassed in the COVID pandemic is now paving the path to pharma nirvana: a weight loss pill likely worth hundreds of billions.” Pfizer is also hoping to develop blockbuster drugs for diabetes, migraines, ulcerative colitis, prostate cancer and sickle cell disease, and is gobbling up smaller drug companies with promising product portfolios.

A blockbuster drug may rake in billions, but that doesn’t mean it’s a blockbuster in the sense that it’s effective, as we’ve seen with Paxlovid and the mRNA COVID shot. Pfizer gets around this in large part by being a “remarkable marketing machine,” to quote Timothy Calkins, a professor of marketing at Northwestern University’s Kellogg School of Management.6

Not only is Pfizer spending big bucks on splashy advertising, they also work with contract research firms like ICON, which run medical research trials for drug companies and federal agencies alike, thereby giving the drug companies the inside track on drug approvals.7 8

Pfizer also gets plenty of free help from the federal government which, in the case of COVID, coerced millions with job loss threats into getting the shots, and implemented rules that ensure hospitals and pharmacies will only prescribe certain COVID drugs, Paxlovid being one of them.

In a November 4, 2022, article,9 clinical and public health physician Dr. David Bell discusses the art — and price — of lying, noting that the more divorced a lie is from reality, the more likely it is to succeed, thanks to the quirks of human nature and normal psychology:

“In a former role I had a boss who lied a lot. The lies were pure fantasy, but massive in scope and delivered with sincerity. They were very successful.

This success was based on the reluctance of most people to consider that someone in a position of authority in a humanitarian organization would completely ignore all semblance of reality. People assumed the claims must be true as fabricating information to that extent in those circumstances seemed to defy logic.

The principle of Really Big Lies is based on the lies being so divorced from reality that the listener will assume their own perception must be flawed, rather than doubt the claims of the person telling the lies. Only an insane or ridiculous person would make such outlandish claims, and a credible institution would not employ such a person.

Therefore, given that the institution is apparently credible, the statements must also be credible, and the listener’s prior perception of reality was therefore flawed. Lesser lies, by contrast, are likely to be perceived as sufficiently close to known reality to be demonstrably wrong. Inventing truth can be more effective than bending it.”

I believe this is precisely the strategy employed by Big Pharma, health agencies, government officials and the deep state propaganda arm over the past three years. Their claims have been so far from any semblance of reality, anyone aware of the facts has been left feeling more than a little crazy.

Unfortunately, while most humans have a moral and ethical compass, few end up following it when confronted by psychopaths in authority and the peer pressure to conform. As noted by Bell, good team players almost always end up supporting false narratives, and those who refuse to go along with what are clearly lies tend to be but a tiny minority.

For decades, patient-centered health care has been the norm, and patients not only had the right, but the duty, to participate in the planning and implementation of their care. This was enshrined in the 1978 Declaration of Alma Ata10 — a declaration adopted by the World Health Organization “as the key to achieving an acceptable level of health throughout the world.”

However, as noted by Bell, centralized top-down health care is far more attractive to Big Pharma investors. The primary obstacle to the corporatization and monetization of public health was truth, and this obstacle was finally (and formidably) overcome during the COVID pandemic. Bell explains:11

“COVID-19 proved that even this impediment to progress can be expunged through consistent lying and the vilification of truth-tellers, backed by a well-managed behavioral psychology campaign.

This pandemic response provided a template not only for vastly-increased corporate income, but for job certainty and expansion of opportunity for the army of mostly-Western bureaucrats and health professionals filling the offices, meeting rooms and business-class seats of its implementing organizations. COVID-19 made corporate colonialism respectable again.

Superficially, COVID-19 appears a poor disease choice to facilitate a fundamental societal reset.

Death is heavily concentrated in old age … Severe cases are generally confined to those with life expectancies already shortened by metabolic diseases … Countries that failed to implement measures to restrict and impoverish their people … had COVID-19 outcomes similar to those that opted for lockdowns and other trappings of medical fascism.

Average hospital admissions in the UK and USA declined during the pandemic, not what the public expects when a pathogen wreaks havoc. Lockdowns devastated economies … COVID vaccines have also been unhelpful as high vaccination rates failed to noticeably impact infection and transmission …

Thus, COVID-19 provided a hard bucket of facts to deal with, but this is just the situation in which Really Big Lies can work. These were needed both to fool the public, and to provide a structure within which health professionals could implement the policy.

Largely by playing on fear, divorcing data from context, and disseminating false information widely and incessantly, a whole new belief system has been constructed in public health to replace the evidence-based orthodoxy of former years.

Reality has been replaced with dogma so divorced from any basis in fact that it is easier to go with the propaganda than deal with the dissonance that would otherwise result.”

The new fantasy-based beliefs that health care workers, patients, researchers, academics and public health employees are now forced to embrace include the following, quoted from Bell’s article:12

  • Disease burden should be measured in raw mortality, and not include metrics such as life-years lost. Hence an 85-year-old dying of a respiratory virus is equivalent to a 5-year-old dying of malaria in terms of burden and urgency;

  • Medium and long-term harms due to poverty and reduced healthcare access should not be considered when assessing the value of an intervention. A modelled effect on the target pathogen is the only relevant metric;

  • It is appropriate to misinform the public on age-related risk and relative disease burden and better to instill fear in order to achieve compliance with public-health directives;

  • Growth of viral transmission in a community follows an exponential curve, rather than a steady deceleration (e.g. Gompertz curve) as the proportion of recovered (immune) people accumulate;

  • Banning students from school for a year protects the elderly, while not locking in generational poverty;

  • Cloth and surgical masks stop aerosolized virus transmission, and all meta-analyses of randomized control trials (that show minimal or no effect) should be ignored;

  • Post-infection immunity to respiratory viruses is expected to be poor and short-lived, whilst vaccines to a single viral protein will somehow produce much stronger immunity;

  • Immunity to viruses is best measured by antibody concentrations rather than T-cell response or clinical outcomes;

  • Informed consent for vaccination should not include information on demonstrated risks, as this could promote ‘vaccine hesitancy’;

  • It is appropriate to give a new gene-based pharmaceutical class in pregnancy that crosses the placenta without any pregnancy trial data, toxicology studies, or long-term outcomes data (in anyone);

  • Irrespective of the Convention on the Rights of the Child ‘In all actions concerning children … the best interests of the child shall be a primary consideration,’ it is appropriate to inject children with drugs lacking long-term safety data in order to protect the elderly;

  • Pandemics are becoming more frequent and more deadly, despite the historical record, and the progress of modern medicine, indicating quite the opposite.

As Bell correctly points out, these new public health positions are not just slightly incorrect. They’re all “either unethical or clear nonsense, contradicted by prior public health orthodoxy.” Indeed, most are classical Orwellian doublespeak and 180 degrees from the truth.

But it’s the sharp break from factual reality that makes it impossible to question them because, if you do, you’re now questioning “the entire current hierarchy of public health,” Bell says.

To quote Dr. Anthony Fauci, you’re not attacking him when you question his irrational flip-flopping, you’re questioning science itself. If you question any of these fantasy-based beliefs, you’re now a science-denier, and you’re putting your employment and reputation at risk. Unfortunately, those risks are not imaginary.

“The way out of this is simply to refuse to lie, or cover for the lies of others … [The] truth will catch up, one day, with those who don’t … It is far better to leave early and live with dignity.” ~ Dr. David Bell

The punishment for refusing these false narratives is very real and very severe. Many doctors and scientists whose reputations and contributions to public health have been beyond reproach for decades have been stripped of their medical licenses and lost their jobs for speaking out against these COVID fallacies.

So, where do we go from here? How do we end the madness and return to reality-based public health?

“Whilst growing their industry’s finances, public health professionals are degrading themselves and betraying society,” Bell writes.13 “The betrayal, based on incessant lying, is something for which they will inevitably face consequences …

Eventually, even the most dedicated followers will begin to question the sense of putting on a mask at a restaurant door only to remove it 10 steps later, or vaccinating vast populations against a disease to which they are already immune whilst they die of other readily preventable diseases.

The way out of this is simply to refuse to lie, or cover for the lies of others … [The] truth will catch up, one day, with those who don’t … It is far better to leave early and live with dignity.”

If you’re paying attention, you’ve undoubtedly noticed that many drug companies, Pfizer in particular, are in the business of creating their own markets. Pfizer released a COVID jab that neither protects against infection nor prevents spread, thereby necessitating multiple boosters. Its antiviral COVID drug Paxlovid causes rebound, necessitating multiple doses.

Now we find that the COVID jabs are also associated with increased rates of respiratory syncytial virus (RSV) infection in children, and like clockwork, Pfizer and Moderna start working on RSV jabs. The CDC also aids by recommending kids get additional COVID shots. Is this a racket or what!?

The Informed Consent Action Network (ICAN) is now demanding answers from the CDC about the off-season spike in RSV rates,14 which mysteriously arose in the wake of childhood injections against COVID.

Moderna’s pediatric COVID jab trial showed those who got the jab had higher rates of RSV than the placebo group. RSV was also one of the primary serious side effects in Pfizer’s pediatric trial. Now, all of a sudden, we’re seeing out-of-season RSV spikes in children. Coincidence? Make them prove it. In a legal update, ICAN reports:

“The issue is so serious that even the FDA’s vaccine committee, VRBPAC, which normally cheerleads even the most dangerous vaccine, noted the correlation and ‘stressed the importance of continued post-authorization safety surveillance, in particular for … certain respiratory infections (RSV and pneumonia) in the youngest age group …’15

Despite the noted importance of surveilling RSV post-authorization, no one at CDC or FDA seems to be drawing a connection between the increase in RSV and the COVID-19 vaccines being administered to children.

Incredibly, the CDC just issued an ‘Official Health Advisory’16 about the increase RSV and respiratory virus cases and, in it, the CDC recommends all individuals 6 months and up receive an influenza vaccine and a COVID-19 vaccine!

Not surprisingly, the press has missed the mark, too. While there are numerous articles detailing the troubling increase in sick children, none reference COVID-19 vaccination despite the data from the manufacturers’ trials.

To get to the bottom of this, on October 26, 2022, ICAN’s attorneys sent a letter17 to the CDC observing the clinical trial data showing a correlation between increased RSV cases and receipt of a COVID-19 vaccine. ICAN’s letter demanded to know the percentage of children who tested positive for RSV and who had received a COVID-19 vaccine prior to their RSV diagnosis.”

In related news, we also have a November 2022 study18 in Nature Communications, which questions the rationale of current booster campaigns. According to the authors:

“An important aspect of vaccine effectiveness is its impact on pathogen transmissibility, harboring major implications for public health policies. As viral load is a prominent factor affecting infectivity, its laboratory surrogate, qRT-PCR cycle threshold (Ct), can be used to investigate the infectivity-related component of vaccine effectiveness …

By analyzing results of more than 460,000 individuals, we show that while recent vaccination reduces Omicron viral load, its effect wanes rapidly. In contrast, a significantly slower waning rate is demonstrated for recovered COVID-19 individuals.

Thus, while the vaccine is effective in decreasing morbidity and mortality, its relatively small effect on transmissibility of Omicron (as measured here by Ct) and its rapid waning call for reassessment of future booster campaigns.”

Considering the theoretical protection of these shots last for just 70 days (according to this study), are the risks associated with the shots really worth it? So far, several risk-benefit analyses have all come to the conclusion that the risks far outweigh any potential benefit.

Unfortunately, it seems we have to rely on scientists outside the U.S. to do this kind of bench science, as all we seem get from American research institutions are analyses of how to get “anti-vaxxers” to buy the false narrative and roll up their sleeves.

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Disclaimer: The entire contents of this website are based upon the opinions of Dr. Mercola, unless otherwise noted. Individual articles are based upon the opinions of the respective author, who retains copyright as marked.

The information on this website is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended as a sharing of knowledge and information from the research and experience of Dr. Mercola and his community. Dr. Mercola encourages you to make your own health care decisions based upon your research and in partnership with a qualified health care professional. The subscription fee being requested is for access to the articles and information posted on this site, and is not being paid for any individual medical advice.

If you are pregnant, nursing, taking medication, or have a medical condition, consult your health care professional before using products based on this content.

C-19 Injections: Massive Regulatory and Manufacturing Fraud

c-19 injections regulatory and manufacturing fraud

By: Tessa Lena

  • Alexandra Latypova is an ex-pharmaceutical industry and biotech executive with a lot of experience in the areas of drug safety and clinical trials

  • Early on, she discovered that, based on the number of reported deaths and adverse events per lot, there was unprecedented variability in the toxicity of the product

  • According to Alexandra, the mRNA shots do not conform to their label specifications, and “in practice, both ‘blank’ and ‘lethal’ vials and anything in between is produced”

  • Having analyzed massive amounts of publicly available data, as well as documents that became available as a result of FOIA requests and other sources, she has found strong evidence of manufacturing and regulatory fraud

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I recently had the pleasure of interviewing Alexandra Latypova, an ex-pharmaceutical industry and biotech executive, who has been investigating and exposing manufacturing and regulatory fraud related to COVID injections.

We talked about the industry standards that were not adhered to during the clinical trials and the manufacturing of those injections, about the vial content quality testing procedures that had not been put in place, about the “hot batches” and their geographical distribution, about signs of fraud at every stage of testing and manufacturing the product, and about the general condition of living in a world run by a mob.

The latter was the lightest part of our conversation — evoking a lot of dark Eastern European humor — since both of us are Soviet expats, and in 2020, neither of us required a whole lot of imagination to embrace the existential possibility of living in a world run by a mob. We had seen it in the past without a disguise — and when something looks like a duck, walks like a duck, and quacks like a duck, maybe it’s just a duck!

Alexandra grew up in Soviet Ukraine and immigrated to America in the late 1990s. She received her MBA from Dartmouth College and the spent about twenty five years in pharmaceutical industry and biotech (including in the areas of drug safety and clinical trials).

Alexandra has had a very gratifying entrepreneurial career. She has founded a number of successful startups, sold them — all before COVID — and retired, hoping to focus on enjoying her life and especially painting, which she does masterfully.

When 2020 knocked on the door with a whole bag of ugly and weird “new normal” treats, Sasha smelled the rat right away. Initially, she became alarmed by the abnormalities in “COVID response,” including the very conspicuous campaign to prevent effective treatment of COVID.

Compelled to understand what was going on, Alexandra got to work. She looked at VAERS and discovered huge discrepancies between the lots, where some batches had just a few reported severe adverse events, and some had over 1500 (she later learned from FOIA’ed documents that lot sizes were in a relatively similar range, and thus the discrepancies could not be explained by the lot size).

And when it comes to VAERS, let’s not forget the 2010 Harvard Pilgrim study showing that VAERS was severely underreported — NOT overreported — capturing less than 1% of adverse events.

Early on, Alexandra discovered the existence of “hot batches.” She is one of team members behind the famous “How Bad Is My Batch” webpage where people can look up the number of severe adverse events reported to VAERS associated with a COVID injection lot number. Other fearless members of the team are Dr Mike Yeadon, ex-head of Pfizer Respiratory Research, Jessica Rose, statistician, Craig Paardekooper, researcher, and Walter Wagner, lawyer.

The slide below show the unprecedented variability of serious adverse events and deaths in the U.S. per batch. Note the comparison to the variability of the flu vaccine lots.

covid-19 vaccines serious ae and deaths

In the interview, Alexandra also mentioned the uneven distribution of deaths per a hundred thousand doses from batch to batch in the U.S. The coasts did much better than some of the Midwestern states that showed a very high numbers of reported deaths per a hundred thousand doses. The worst state is South Dakota (30+ reported deaths per 100,000 doses).

The areas that did even worse, according to Alexandra, were some of the U.S. territories with high percentage of indigenous population. (The latter data became available after the presentation was created, not reflected in the slide.)

vaers deaths 100k after vaccination

In the interview, Alexandra calls the COVID injections products “garbage soup,” both due to the massive non-compliance of the vial content to the specifications (per multiple independently done tests) — as well as due to their non-compliance with Good Manufacturing Practices. Wait, are the manufacturers trolling us? Are telling us that they do not comply (but we must)?!

There are many theories about what’s behind for such wild inconsistency between batches, from manufacturing defects to deliberate toxicity testing — and anything in-between. In her TrialSiteNews article, Alexandra tackles one important angle of the challenge that so many of us had to “explain” when talking to the friends of a more mainstream persuasion:

“Many of us are familiar with the following conundrum: on one hand, highly credentialed scientists and doctors have written numerous research papers explaining the dangerous mechanisms of action underlying mRNA/DNA “platform” technologies. The papers are meticulously researched and depict, correctly in my opinion, many terrifying consequences of the technology that breaches the innate protective mechanisms of human cells.”

“Furthermore, these theoretical papers are validated by the observed outcomes, such as for example, increases in all-cause mortality in high correlation with increases in rates of vaccination in a given territory, unprecedented increases in the adverse events and deaths recorded by various passive reporting systems, astonishingly high reports of the adverse events and deaths from the pharmas’ own pharmacovigilance systems, and autopsy findings in vaccinated post-mortem showing the mechanisms of mRNA technology damage in histopathologic evaluations.

On the other hand, many who have received the injections report no adverse effects and deem the points above a ‘crazy conspiracy’.”

“The question from the uninjured seems to be – why don’t we see MORE deaths if what you say about mRNA products is true? Setting aside ethical limitations of this question, here is a possible answer why: The mRNA shots do not conform to their label specifications. In practice both “blank” and “lethal” vials and anything in between is produced [emphasis mine].

Like I wrote earlier on my Substack, “remarkably, some analyzed vials were reported to contain left over magnetic beads (magnetic beads are used in production of mRNA). Remember the “crazy” videos of some people developing magnetism in the place of injection? Now we have a new, ‘non-conspiratorial’ explanation for the ‘conspiratorial’ videos! Yay, following the science!”

According to Alexandra, vials of mRNA injections are not routinely tested by the manufacturers for conformity to the label. She notes that “the more they conform to the mRNA specification, the deadlier they seem.”

The only vial-level tests specified, for instance, by Pfizer, in leaked Chemistry Manufacturing and Controls documents, are the vial weight at filling, manual inspection for large visible particles, and some tests related to integrity such as vial capping.

The documents don’t describe no routing vial or dose tests verifying the ingredients. Each Pfizer dose is supposed to contain 30 mcg of mRNA, as stated on the label, but there is no information about any testing done to verify that.

“The ingredient conformity tests described in Pfizer CMC package are based on the bulk product batch testing – an upstream manufacturing process step.

It is a regulatory requirement to retain samples of each batch produced, and these samples of vials should exist and be available for examination. Per contracts with the US Government/DOD, the product is shipped to the DOD who retains the ownership of the vials until the product is injected into people.”

Alexandra notes that those contracts are very detailed and specify manufacturing data to be delivered to the DOD, however, she not find any descriptions of sampling of the vials for purposes of verification of their contents vs the label. “Furthermore, it is expressly forbidden by the international vaccine supply contracts to perform the vial tests for label conformity.”

In the interview, as well as in this article, Alexandra talks about the evidence of collusion between the manufacturers, the global regulatory agencies, and the US Department of Defense.

Having analyzed various public data from CDC’s VAERS database as well as various documents that have been obtained through FOIA releases and other source, she concluded that such collusion “led to the commercial release of the Covid-19 countermeasures that do not comply with the current Good Manufacturing Practices (cGMP).”

Evidence that Alexandra talks about includes Moderna’s non-clinical study summaries, Pfizer’s Chemistry Manufacturing and Controls documentation, and contracts between pharma and the DOD for supply of the mRNA/DNA products. According to her, “it reveals disregard for established safety rules, regulations, and safety practices throughout the development, manufacture, and distribution of these products.”

As reported by Children’s Health Defense, Alexandra reviewed 700 pages of documents that Moderna submitted to the FDA as part of its application process and obtained via a Freedom of Information Act request.

And according to her, “out of nearly 700 pages, about 400 pages are irrelevant studies that Moderna repeated multiple times. Moderna also submitted three versions of a single module, she said. And one module contained only narrative summaries of Moderna’s studies, but no actual study results.” Alexandra’s conclusion is that we are missing a large number of results, such as full reports that would support their narrative.

“The FDA ‘obviously did not object’ to any of this, she said. ‘That’s evidence of collusion to me with the manufacturer.’”

Other “abnormalities” that Alexandra highlighted both in the interview and in the Children’s Health Defense article, were Moderna’s clinical trials timeline and the fact that their product has two — not one — Investigational New Drug (IND) number.

Normally, there is one IND application for one product. “In this case, however, there are two IND applications — one belonging to Moderna, and one belonging to the National Institutes of Health, which partnered with Moderna on its COVID-19 vaccine.”

“The Investigational New Drug (IND) application meeting is supposed to occur with the FDA when the company initiates human clinical trials. Moderna and the FDA had a pre-IND meeting on Feb. 19, 2020, and the IND application was formally opened the next day. The global pandemic was declared on March 11, 2020.”

In the words of Alexandra, “Somehow these visionaries could predict the future with such certainty that they opened a clinical trial for the vaccine, for which a pandemic was announced a month later.”

As Alexandra notes in her article titled, “Did Pfizer Perform Adequate Safety Testing for its Covid-19 mRNA Vaccine in Preclinical Studies? Evidence of Scientific and Regulatory Fraud,” “both the manufacturer and the regulators behaved in a highly dishonest manner and conspired to push an entirely novel technology and product on millions of people without carrying out a single well designed safety assessment.”

For example, she points out that a review of clinical studies released by FOIA uncovered that at least 4 different variants of active ingredient were included in the single Investigational New Drug application by Pfizer IND#19736:

  • BNT162a1 — Unmodified mRNA (uRNA; variant RBL063.3)

  • BNT162b1 — Methylpseudouridine-modified mRNA (modRNA; variant RBP020.3)

  • BNT162b2 — Methylpseudouridine-modified RNA (modRNA; variant RBP020.2)

  • BNT162c2 — Self-amplifying unmodified mRNA (saRNA; variant RBS004.2)

Alexandra writes that while the use of multiple versions of a product in the early stages of development is often inevitable, each chemical or biological entity is nevertheless deemed legally distinct for the purpose of product approval.

“Therefore, studies conducted with versions of the product that don’t conform to the exact specification of the final version may serve only as supporting information for the approval of the latter, but they should never be deemed definitive and sufficient tests for claims of safety or efficacy pertaining to the final product.”

She further mentions that in September 2021, the FDA issued a draft guidance entitled “Studying Multiple Versions of a Cellular or Gene Therapy Product in an Early-Phase Clinical Trial,” which states that each version of product requires a separate IND application.

However, stunningly, “a footnote in this guideline exempts ‘vaccines intended to prevent infectious diseases’ from this requirement. No explanation is given as to why this exemption is made, and no conceivable scientific or legal basis exists for this exemption, other than that the FDA had already arbitrarily allowed this unprecedented deviation from the regulatory standard and later needed to cover their tracks.

In fact, arguably this regulatory ‘exception’ does not even apply to Pfizer’s COVID-19 ‘vaccine,’ since the product does not prevent infection or transmission of the disease. Is intent to prevent illness alone a sufficient condition? After all, every new drug is intended to do something like preventing an illness, but only few successfully do so.”

Alexandra’s article is very detailed, and I highly recommend reading it in full. You can also find Alexandra on TrialSiteNews and on her Bitchute channel. To summarize her take on Pfizer, she make the following points:

  • Pfizer’s program did not include a comprehensive end-to-end test of all components of the final approved product (the mRNA COVID-19 vaccine). Instead, the studies included in the document package submitted to the FDA employed several variants and analogues of the product, whose comparability to the actual COVID-19 vaccine was not demonstrated or evaluated.

    Thus, no comprehensive assessment of product safety can be made on the basis of these studies.

  • A key determinant of a drug’s toxicity is its distribution within the body. However, with the mRNA active ingredient of Pfizer’s COVID-19 vaccine, this crucial aspect was never studied!

  • Pfizer claimed absence of potential for “vaccine-elicited disease enhancement” based on studies of an animal species that does not get sick from SARS-CoV-2.

  • The CDC, the FDA and Pfizer all lied about “vaccine staying at the injection site;” they knew all along that distribution of the vaccine throughout the body had to be expected.

  • Pfizer skipped major categories of safety testing altogether.

  • Pfizer used dishonest and self-serving interpretation of regulatory guidelines to justify the shortcuts it took in routine safety testing.

  • Both FDA and Pfizer knew about major toxicities associated with gene-therapy medicines in general, and they therefore cannot claim lack of anticipatory knowledge of these risks with the particular gene therapy medicine that is Pfizer’s COVID-19 vaccine. This points to intentional fraud and collusion between Pfizer and the regulators, who conspired to push this untested dangerous product on the market.

Even though it is rather disheartening to know we live in a world that run by a mob, the challenge is centuries old, and remembering it can bring us much needed perspective and balance. The novel and “sudden” part of the challenge is that is happening to us, here and now, in broad daylight. That’s shocking! But throughout history, many of our ancestors had to deal with tyrants, and today, it is our turn to be brave. May our brave ancestors be our inspiration.

I would like to end this story with a short quote from my earlier article titled, “Is Our World Run Like a Mafia? So What Do We Do?:”

“Good news: As the mafia bosses do their predatory thing, something mysterious is happening the hearts of those of us who insist on love. Under pressure, we are forced to remember that we are not theirs.” We are not theirs. It is true.

To find more of Tessa Lena’s work, be sure to check out her bio, Tessa Fights Robots.

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Disclaimer: The entire contents of this website are based upon the opinions of Dr. Mercola, unless otherwise noted. Individual articles are based upon the opinions of the respective author, who retains copyright as marked.

The information on this website is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended as a sharing of knowledge and information from the research and experience of Dr. Mercola and his community. Dr. Mercola encourages you to make your own health care decisions based upon your research and in partnership with a qualified health care professional. The subscription fee being requested is for access to the articles and information posted on this site, and is not being paid for any individual medical advice.

If you are pregnant, nursing, taking medication, or have a medical condition, consult your health care professional before using products based on this content.