EU, U.K. Join U.S. in Launching Online ‘Disinformation’ Policies, Prompting Concerns About ‘One-World Governance’ of Social Media

The European Union’s Digital Services Act (DSA) and the U.K.’s proposed Online Safety Bill are among the latest government policies designed to hold social media companies responsible for hate speech and “disinformation” posted by users.

Experts interviewed by The Defender expressed concerns about the potential slippery slope of regulations — in the U.S. and overseas — which, under the guise of “combating disinformation,” stifle the spread of information deemed inconvenient for governments and other powerful actors.

As reported by The Defender, in the U.S., these proposals include a government “disinformation board” and a bill pending before Congress, the Digital Services Oversight and Safety Act.

The EU’s new regulations, experts said, may have far-reaching impacts beyond Europe.

Michael Rectenwald, author of “Google Archipelago: The Digital Gulag and the Simulation of Freedom,” said he can foresee a future in which such regulations might affect all speech — not just speech on social media platforms.

Rectenwald told The Defender:

“[T]he EU’s DSA represents a major step toward one-world governance of social media and Internet search and one step closer to global government.

“Since the distinction between ‘on-line’ and ‘off-line’ activity will lose all meaning as the Internet includes the Internet of Things and Bodies, the DSA may become the law of the land.”

Is EU’s Digital Services Act on collision course with Musk’s Twitter plans?

In timing that coincided with Elon Musk’s intent to purchase Twitter, the EU announced April 23 the passage of the Digital Services Act (DSA).

The DSA seeks to tackle the spread of “misinformation and illegal content” and will apply “to all online intermediaries providing services in the EU,” in proportion to “the nature of the services concerned” and the number of users of each platform.

According to the DSA, “very large online platforms” (VLOPs) and “very large online search engines” (VLOSEs) — those with more than 45 million monthly active users in the EU — will be subject to the most stringent of the DSA’s requirements.

Big Tech companies will be obliged to perform annual risk assessments to ascertain the extent to which their platforms “contribute to the spread of divisive material that can affect issues like health,” and independent audits to determine the steps the companies are taking to prevent their platforms from being “abused.”

These steps come as part of a broader crackdown on the “spread of disinformation” called for by the Act, requiring platforms to “flag hate speech, eliminate any kind of terrorist propaganda” and implement “frameworks to quickly take down illicit content.”

Regarding alleged “disinformation,” these platforms will be mandated to create a “crisis response mechanism” to combat the spread of such content, with the Act specifically citing the conflict between Russia and Ukraine and the “manipulation” of online content that has ensued.

The DSA also will ban certain types of advertising on digital platforms, including targeted ads tailored to children or to people of specific ethnicities or sexual orientations.

Tech companies also will be required to increase transparency in the form of providing regulators and researchers “access to data on how their systems recommend content to users.”

This latter point appears similar to Musk’s plans to make Twitter’s algorithms “open source to increase trust.”

Companies violating the provisions of the DSA would risk fines of up to 6% of their total global annual revenue, while repeat offenses may result in the platforms being banned from the EU — despite the “open internet” principle professed by the principle of “net neutrality” enshrined in EU law.

According to Techcrunch, the DSA will not fully come into effect until early 2024. However, rules for VLOPs have a shorter implementation period and may be enforced by early 2023.

A spokesperson for the European Commission — the EU’s executive branch — said the new regulations will ensure Big Tech’s “power over public debate is subject to democratically validated rules, in particular on transparency and accountability.”

Margrethe Vestager, the vice president of the European Commission, added, “With today’s agreement we ensure that platforms are held accountable for the risks their services can pose to society and citizens,” and, “With the DSA we help create a safe and accountable online environment.”

Directly addressing Musk, the European Commission’s internal market commissioner, Thierry Breton, tweeted, “Be it cars or social media, any company operating in Europe needs to comply with our rules — regardless of their shareholding. Mr. Musk knows this well,” adding, “[Musk] is familiar with European rules on automotive [referring to Musk’s ownership of Tesla Motors], and will quickly adapt to the Digital Services Act.”

Separately, Breton stated, “We welcome everyone. We are open but on our conditions. At least we know what to tell him: ‘Elon, there are rules. You are welcome but these are our rules. It’s not your rules which will apply here.’”

Breton’s warning to Musk bears a striking resemblance to the statements of then-German finance minister Wolfgang Schaeuble, who in 2015 warned the newly elected left-wing Greek government not to entertain thoughts about renegotiating the austerity measures imposed on the country by the EU and International Monetary Fund, stating, “Elections change nothing. There are rules.”

Voice of America, a media outlet reflective of official U.S. government policy, reported “the job of reining in a Musk-led Twitter could fall to Europe,” referring to the DSA.

According to Gizmodo, the EU’s new legislation “could have global reverberations,” adding, “Lawmakers are also hoping it could serve as a model for other countries like India and Japan.”

However, Gizmodo warns the success of the DSA in accomplishing its objectives is far from guaranteed, referring to the example of the EU’s General Data Protection Regulation (GDPR): “Some predicted [the GDPR] would fundamentally shift online privacy protection worldwide, and instead [it] basically just gave us those insufferable cookie permission pop-ups.”

While the DSA would apply to all 27 EU member states, some of these countries have already enacted similar domestic legislation. For instance, Germany has regulations in place that require digital platforms to remove hate speech within 24 hours or face fines of up to €50 million ($56 million).

Techcrunch, in reporting on the passage of the DSA, referred to legislation in countries not frequently noted for their democratic traditions or respect for free speech, such as China, Turkey, India and Nigeria.

As Techcrunch stated, platforms in these countries found to be “non-compliant” with domestic mandates may face fines, police raids, shutdowns and prison sentences for their executives.

Similar regulations pending in U.K.

Legislation similar to the DSA, the Online Safety Bill, is pending in the U.K. It would require Big Tech platforms to moderate “illegal” and “harmful” content in order to be allowed to operate in the U.K.

The bill would require digital platforms to protect users from such “harmful” content, with the threat of fines of up to 10% of global turnover for companies found in violation, as well as potential prison time for senior managers of these companies in cases of non-compliance.

A spokesperson for the U.K. government said:

“Twitter and all social media platforms must protect their users from harm on their sites.

“We are introducing new online safety laws to safeguard children, prevent abusive behaviour and protect free speech.

“All tech firms with users in the U.K. will need to comply with the new laws or face hefty fines and having their sites blocked.”

Max Blain, a spokesperson for U.K. prime minister Boris Johnson, said, “Regardless of ownership, all social media platforms must be responsible” for “protecting” users.

As The Defender recently reported, Damian Collins, a member of the British parliament with the British Labour Party who led a parliamentary committee that developed the Online Safety Bill, is a board member of the Center for Combating Digital Hate, which partners with prominent “fact-checking” firm NewsGuard.

As previously reported by The Defender, NewsGuard, in turn, closely collaborates with the World Health Organization (WHO), which also recently expressed concerns about Musk’s purchase of Twitter.

As U.S., EU  sign commitment to ‘democratic values’ on the internet as they prepare policies to regulate online speech

Overshadowed by the news of Musk’s Twitter purchase and developments such as the DSA and the Biden administration’s “disinformation board,” several dozen countries quietly signed the “Declaration for the Future of the Internet” April 28.

Fifty-six countries and entities, including the U.S. and the EU, signed this declaration, described as “a political commitment to push rules for the internet that are underpinned by democratic values” and a response to Russia “wielding internet disruptions as a part of its escalating attacks on Ukraine.”

U.S. News reports that the declaration — which is not legally binding — is the first of its kind globally, and “protects human rights, promotes free flow of information, protects the privacy of users, and sets rules for a growing global digital economy among steps to counter what two Biden administration officials called a ‘dangerous new model’ of internet policy from countries such as Russia and China.”

According to the U.S. State Department, the declaration’s principles include:

  • Protect human rights and fundamental freedoms of all people.

  • Promote a global Internet that advances the free flow of information.

  • Advance inclusive and affordable connectivity so that all people can benefit from the digital economy.

  • Promote trust in the global digital ecosystem, including through protection of privacy.

  • Protect and strengthen the multi-stakeholder approach to governance that keeps the Internet running for the benefit of all.

In turn, the declaration was described by the EU as being “in line with the rights and principles strongly anchored in the EU.”

EU Commission President Ursula von der Leyen, known for her strong support of digital “vaccine passports” throughout the EU, stated:

“Today, for the first time, like-minded countries from all over the world are setting out a shared vision for the future of the Internet, to make sure that the values we hold true offline are also protected online, to make the Internet a safe place and trusted space for everyone, and to ensure that the Internet serves our individual freedom.

“Because the future of the Internet is also the future of democracy, of humankind.”

Thierry Breton remarked:

“This Declaration will ensure that the Internet and the use of digital technologies reinforce, not weaken, democracy and respect for human rights.”

According to the State Department, “[t]he Declaration remains open to all governments or relevant authorities willing to commit and implement its vision and principles.”

What does all this mean for Musk, Twitter and the future of free speech online?

Social media analysts and experts expressed varying opinions and predictions as to what regulations such as the DSA may mean for the global operations of digital platforms such as Twitter — especially if Musk attempts to make good on his pledges to “restore free speech.”

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Vasilis Vasilopoulos, data protection officer with Greek public broadcaster ERT and a Ph.D. candidate in journalism and mass media studies at Greece’s Aristotle University, told The Defender there are some positive elements to the DSA.

However, the boundaries of what is considered free speech should also be expanded, albeit within certain limits, he said.

Vasilopoulos added:

“The DSA is not the only means through which the problem of unethical [social media] algorithms with deceptive motives, or the unethical use of social media platforms, can be solved.

“[I]t is obvious that these platforms have surpassed the limits to democracy that we believed existed, and therefore, it is important that instead of imposing restrictions, we expand these boundaries, in favor of humanity and not capital or power.”

Matthew Spitzer, professor at Northwestern University’s Pritzker School of Law, said the EU’s proposals in particular may clash with Musk’s stated goals for Twitter, telling The Defender:

“[The DSA] may interfere with one of Elon Musk’s stated goals for buying Twitter. He seems to want less content moderation. But this regulation requires a lot of it.

“Second, this regulation dovetails with Musk’s stated desire for increased transparency. He had promised more transparency.”

Spitzer added his view that the DSA will likely increase the cost of operation for all social media companies, especially if they must also conform to domestic laws passed by various EU member states.

He added that U.S. tech companies may represent an easy target for European regulators, telling The Defender:

“[T]here will be conflicts between the USA and Europe … all of the target companies started in the USA. They are easy political targets in Europe.”

Referring specifically to Elon Musk and Twitter, Rectenwald said:

“If Musk is to have his way, the platform would no longer discriminate against content based on ‘wokeness,’ political beliefs, or the adherence to official state narratives and dictates.

“This could include the restoration of banned accounts on request by users and dramatic changes to Twitter’s discriminatory, leftist algorithms.”

According to Rectenwald, the EU’s regulations may “hamstring” Musk’s vision for Twitter and lead to a one-size-fits-all approach to content moderation, resulting in a “slippery slope” wherein “any information and opinion that differs from WHO-established official narratives regarding pandemics or other health-related crises” would be restricted.

Rectenwald said:

“Most likely, in order to meet the EU’s regulatory requirements and to streamline their efforts, VLOPs and VLOSEs will simply apply one set of rules to all online content.”

He also added that further pressures on platforms like Twitter may come not from EU regulators, but from the tech industry itself:

“[P]ressure to conform to ‘woke’ dictates will come from the Big Tech ‘woke’ cartel, including threats to remove the Twitter app from the Apple Store for failure to censor ‘hate speech,’ and the flight of ‘woke’ advertisers.

“Most likely, Musk’s purchase of Twitter will make no difference as free speech is further curtailed.”

https://childrenshealthdefense.org/defender/online-disinformation-policies-world-governance-social-media/

Remdesivir ‘Disastrous’ as COVID Treatment, But Government Pays Hospitals to Use It

Story at a glance:

  • So far, all of the drugs developed against COVID-19 have been disastrous in one way or another. Remdesivir, which to this day is the primary COVID drug approved for use in U.S. hospitals, routinely causes severe organ damage and, often, death.

  • Despite that, the U.S. Food and Drug Administration has approved remdesivir for in-hospital and outpatient use in children as young as 1 month old.

  • Another COVID drug, Paxlovid, will in some cases cause the infection to rebound when the medication is withdrawn.

  • Molnupiravir (sold under the brand name Lagevrio) also has serious safety concerns. Not only might it contribute to cancer and birth defects, it may also supercharge the rate at which the virus mutates inside the patient, resulting in newer and more resistant variants.

  • The fact that U.S. health authorities have focused on these drugs to the exclusion of all others, including older drugs with high rates of effectiveness and superior safety profiles, sends a very disturbing message. They’ve basically become extensions of the drug industry, protecting the drug industry’s interests at the cost of public health.

So far, all of the drugs developed against COVID-19 have been disastrous in one way or another. Remdesivir, for example, which to this day is the primary COVID drug approved for use in U.S. hospitals, routinely causes severe organ damage, and, often, death.

Despite its horrible track record, the U.S. government actually pays hospitals a 20% upcharge for sticking to the remdesivir protocol, plus an additional bonus. Hospitals must also use remdesivir if they want liability protection.

Incentives like these have turned U.S. hospitals into veritable death traps, as more effective and far safer drugs are not allowed, and hospitals are essentially forced to follow the recommendations of the U.S. Centers for Disease Control and Prevention.

As reported by Forbes science reporter JV Chamary back in January 2021, in an article titled, “The Strange Story of Remdesivir, a COVID Drug That Doesn’t Work”:

“Remdesivir is an experimental drug developed by biotech company Gilead Sciences (under the brand name Veklury) in collaboration with the US Centers for Disease Control and Army Medical Research Institute of Infectious Diseases …

“The drug proved ineffective against the Ebola virus … yet was still subsequently repurposed for SARS-CoV-2 coronavirus. News media prematurely reported that patients were responding to treatment.

“But the published data later showed that ‘remdesivir was not associated with statistically significant clinical benefits [and] the numerical reduction in time to clinical improvement in those treated earlier requires confirmation in larger studies’ …

“What’s weird about remdesivir is that it hasn’t been held to the same standards as other drug candidates. Normally, a drug is only approved for use by a regulatory body like the U.S. Food and Drug Administration if it meets the two criteria for safety and efficacy.

“Nonetheless, in October 2020, remdesivir was granted approval by FDA based on promising data from relatively small trials with about 1,000 participants. A large-scale analysis by the World Health Organization’s Solidarity trial consortium has cleared up the confusion.

“Based on interim results from studying more than 5,000 participants, the international study concluded that remdesivir ‘had little or no effect on hospitalized patients with COVID-19, as indicated by overall mortality, initiation of ventilation and duration of hospital stay.’ As a consequence of being mostly ineffective, WHO recommends against the use of remdesivir in COVID-19 patients.”

Shockingly, US approves remdesivir for babies

Curiously, while Big Tech — aided and abetted by the U.S. government — has spent the last two years censoring and banning any information that doesn’t jibe with the opinions of the WHO, the U.S. government has completely ignored the WHO’s recommendation against remdesivir.

In fact, in late April, the FDA approved remdesivir as the first and only COVID-19 treatment for children under 12, including babies as young as 28 days, which seems beyond Orwellian and crazy considering it’s the worst of both worlds: It’s ineffective AND has serious side effects.

What’s worse, the drug is also approved for outpatient use in children, which is a first. In an April 30 blog post, Dr. Meryl Nass expressed her concerns about the FDA’s approval of remdesivir for outpatient use in babies, stating:

“Remdesivir received an early EUA (May 1, 2020) and then a very early license (October 22, 2020) despite a paucity of evidence that it actually was helpful in the hospital setting. A variety of problems can arise secondary its use, including liver inflammation, renal insufficiency and renal failure

“WHO recommended against the drug on November 20, 2020. Few if any other countries used it for COVID apart from the US. A large European trial in adults found no benefit. The investigators felt 3 deaths were due to remdesivir (0.7% of subjects who received it). However, on April 22, 2022 the WHO recommended the drug for a new use: early outpatient therapy in patients at high risk of a poor COVID outcome.”

Remdesivir — a reckless choice for children

Nass goes on to recount how monoclonal antibody treatment centers have been turned into outpatient treatment centers using remdesivir instead, but we still don’t have a lot of data on its effectiveness in early treatment. She continues:

“The FDA just licensed Remdesivir for children as young as one month old. Both hospitalized children and outpatients may receive it. The drug might work in outpatients, but the vast majority of children have a very low risk of dying from COVID.

“If 7 deaths per 1,000 result from the drug, as the European investigators thought in the study of adults cited above, it is possible it will harm or kill more children than it saves.

“Shouldn’t the FDA have waited longer to see what early outpatient treatment did for older ages? Or studied a much larger group of children? Very little has been published on children and remdesivir …

“When we look at the press release issued by Gilead, we learn the approval was based on an open label, single arm trial in 53 children, 3 of whom died (6% of these children died); 72% had an adverse event, and 21% had a serious adverse event.”

Overall, remdesivir appears to be an exceptionally risky treatment choice for young children. Certainly, there are safer early treatment protocols that are very effective. Two other COVID drugs, Paxlovid and Molnupiravir, also have serious safety concerns.

Post-Paxlovid COVID rebound

As reported by Bloomberg, COVID patients treated with a five-day course of Paxlovid sometimes experience severe rebound when the medication is withdrawn.

U.S. government researchers are now planning to study the rate and extent to which the drug is causing SARS-CoV-2 infection to rebound, and whether a longer regimen might prevent it.

Bloomberg describes the post-Paxlovid rebound of David Ho, a virologist at the Aaron Diamond AIDS Research Center at Columbia University:

“Ho said he came down with COVID on April 6 … His doctor prescribed Paxlovid, and within days of taking it, his symptoms dissipated and tests turned negative. But 10 days after first getting sick, the symptoms returned and his tests turned positive for another two days.

“Ho said he sequenced his own virus and found that both infections were from the same strain, confirming that the virus had not mutated and become resistant to Paxlovid. A second family member who also got sick around the same time also had post-Paxlovid rebound in symptoms and virus, Ho says.

“‘It surprised the heck out of me,’ he said. ‘Up until that point I had not heard of such cases elsewhere.’ While the reasons for the rebound are still unclear, Ho theorizes that it may occur when a small proportion of virus-infected cells may remain viable and resume pumping out viral progeny once treatment stops.”

  • Clinical Director of the Division of Infectious Diseases at Brigham and Women’s Hospital, Dr. Paul Sax, told Bloomberg:

“Providers who are going to be prescribing this should be aware that this phenomenon occurs, and if people have symptoms worsening after Paxlovid, it’s probably still COVID. The big problem is that when this drug was released, this information wasn’t included [on the label].”

Pfizer defends Paxlovid

The U.S. Food and Drug Administration has stated it is “evaluating the reports of viral load rebound after completing Paxlovid treatment and will share recommendations if appropriate.”

The U.S. Centers for Disease Control and Prevention has not yet commented on the findings.

Pfizer, meanwhile, insists the increase in viral load post-treatment “is unlikely to be related to Paxlovid” because viral rebound was found in “a small number” of both the treatment and placebo groups in Pfizer’s final-stage study.

Clifford Lane, deputy director for clinical research at the National Institute of Allergy and Infectious Diseases (NIAID), told Bloomberg that some people may simply “need longer dosing of Pfizer’s drug than the standard five days.”

“There’s two things that suppress the virus: the drug and the host immune response,” he said. “If you stop the drug before the host immune response has had a chance to kick in, you may see the virus come back.”

Molnupiravir supercharges viral mutation

Molnupiravir (sold under the brand name Lagevrio) also has serious safety concerns. This drug was developed by Merck and Ridgeback Therapeutics and approved for emergency use by the FDA December 23, 2021, for high-risk patients with mild to moderate COVID symptoms.

However, not only might it contribute to cancer and birth defects, it may also supercharge the rate at which the virus mutates inside the patient, resulting in newer and more resistant variants. As reported in November 2021 by Forbes contributor and former professor at Harvard Medical School, William Haseltine, Ph.D.:

“… I believe the FDA needs to tread very carefully with molnupiravir, the antiviral currently before them for approval. My misgivings are founded on two key concerns.

“The first is the drug’s potential mutagenicity, and the possibility that its use could lead to birth defects or cancerous tumors. The second is a danger that is far greater and potentially far deadlier: the drug’s potential to supercharge SARS-CoV-2 mutations and unleash a more virulent variant upon the world …

“My concern with molnupiravir is because of the mechanism by which this particular drug works. Molnupiravir works as an antiviral by tricking the virus into using the drug for replication, then inserting errors into the virus’ genetic code once replication is underway. When enough copying errors occur, the virus is essentially killed off, unable to replicate any further …

“But my biggest concern with this drug is … molnupiravir’s ability to introduce mutations to the virus itself that are significant enough to change how the virus functions, but not so powerful as to stop it from replicating and becoming the next dominant variant.”

Haseltine cites prepandemic experiments showing MERS-CoV and the mouse hepatitis virus (MHV) both developed resistance against the drug, thanks to mutations that occurred.

While the central idea behind the drug is that the genetic errors will eventually kill the virus, these experiments showed the viruses were in fact able to survive and replicate to high titers despite having large numbers of mutations throughout their genomes.

The drug did slow down replication, but as noted by Haseltine, “outside of the lab, as the drug is given to millions of people with active infections, this disadvantage may quickly disappear as we would likely provide a prime selection environment to improve the fitness of the virus.”

This risk may be particularly high if you fail to take all the prescribed doses (typically 800 milligrams twice a day for five days).

Experts question usefulness of Molnupiravir

More recently, in a January 10 article, Newsweek cited concerns by professor Michael Lin of Stanford University:

“‘I am very concerned about the potential consequences now that molnupiravir has been approved … It would only be a matter of time, perhaps a very short time, before a lucky set of mutations occurs to create a variant that is more transmissible or immunoevasive …

“The drug simply speeds up that natural process. The hope is that over enough days all the viral copies will have so many mutations that none of the copies can function.’ But Lin said he was concerned that in the real world, there is a possibility that a mutated virus could jump from a patient taking molnupiravir to another individual, citing the relatively modest efficacy of the drug.

“‘For cases that get worse so that people have to go to the hospital, this drug only prevents that from happening 30% of the time. That means 70% of the time the virus isn’t being eliminated quickly enough to make a difference. And we know COVID patients going to hospitals are highly contagious.’

“Lin said the risks could be heightened when a patient does not comply exactly with the dosing schedule of the drug … ‘In any of those situations viruses will have picked up some mutations but not enough to kill all the virus copies,’ he said. ‘The survivors are now mutated, perhaps have picked up immunoevasion and can go on to infect others’ …

“According to Lin, the ‘very low efficacy alone’ should have disqualified the drug from approval … ‘Even if the drug were great we wouldn’t take such a risk, but this drug is worse than any other drug that’s sought approval for COVID-19. It’s completely not worth it.’”

Haseltine also told Newsweek that, “Of all the antiviral drugs I have ever seen, this is by far the most potentially dangerous,” and “The more people that take it, the more dangerous it will be.”

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One of the FDA panel members who actually voted against the approval of molnupiravir, James Hildreth, president of Meharry Medical College in Tennessee, wanted Merck to do a better job of quantifying the risk of mutations before approval.

During the panel meeting, he noted that:

“Even if the probability is very low, 1 in 10,000 or 100,000, that this drug would induce an escape mutant which the vaccines we have do not cover, that would be catastrophic for the whole world.”

Government has sold out to Big Pharma

Widespread use of a drug that turbocharges mutation of an already rapidly mutating virus probably isn’t the wisest strategy. Likewise, using drugs that cause high rates of organ failure, like remdesivir, and drugs that causes the virus to rebound with a vengeance, like Paxlovid, don’t seem to be in the best interest of public health either.

The fact that U.S. health authorities have focused on these drugs to the exclusion of all others, including older drugs with high rates of effectiveness and superior safety profiles, sends a very disturbing message.

They’ve basically become extensions of the drug industry and have abandoned their original purpose, which is to protect public health — by ensuring the safety and efficacy of drugs, in the case of the FDA, and by conducting critical science and data analysis in the case of the CDC.

Instead, they seem to be doing everything they can to protect Big Pharma profits, even if it costs you your life. Remdesivir, for example, is an extremely expensive drug, costing between $2,340 and $3,120 depending on your insurance.

Ivermectin, meanwhile — which has been very effective against COVID and shown to outperform at least 10 other drugs, including Paxlovid — costs between $48 and $94 for 20 pills depending on your location. The average cost is said to be about $58 per treatment.

Paxlovid costs $529 per five-day course of treatment, and molnupiravir is around $700. While not quite as expensive as remdesivir, both are still nearly 10 times costlier than ivermectin, which is more effective.

Paxlovid alone has cost U.S. taxpayers $5.29 billion. Just imagine the billions we could have saved had we saner leadership.

Since the FDA and CDC cannot be trusted, it’s imperative to take responsibility for your own health. Do your own research and follow your own conscience and conviction.

Remember, when it comes to COVID-19, early treatment is crucial, and effective protocols are readily available — just not from the FDA, CDC or even most hospitals.

For a refresher, check out Dr. Pierre Kory’s interview with Chris Martenson. You can also find many other articles describing early treatment protocols by searching through my Substack archive.

Originally published by Mercola.

https://childrenshealthdefense.org/defender/covid-pills-remdesivir-paxlovid-molnupiravir-cola/

COVID Vaccine Injury Ends Surgeon’s 20-Year Career

Dr. Joel Wallskog was once a successful orthopedic surgeon. A joint replacement specialist for 20 years, he had a large and busy practice in Wisconsin, where he saw almost 6,000 patients each year.

Married to his college sweetheart for almost 30 years and the father of four children, Wallskog had a “fantastic” life, he said. He enjoyed his career and balanced it with fun, active time with his family.

But the Moderna COVID-19 vaccination changed his life forever, Wallskog said. His health deteriorated rapidly and his career came to an end.

He recently told his story to Stephanie Locricchio, an advocacy liaison for Children’s Health Defense (CHD), on CHD.TV’s “The People‘s Testaments.”

In September 2020, Wallskog said, staff members in the clinic he referred patients to began coming down with COVID-19. He did not feel ill (“maybe in retrospect I had a runny nose for a couple days,” he said) but got an antibody test, which was positive.

When a close friend came down with COVID-19 and had to be intubated, Wallskog decided he should get vaccinated, despite his reservations.

“I was part of the healthcare system. I believed in the system,” he told Locricchio.

Still, Wallskog said, “I had some second thoughts. It just didn’t seem right. I just had COVID, I proved that I had antibodies … I had natural immunity. …But again, I was part of the system that I trusted.”

He received his vaccine through his employer, one of the 10 largest healthcare systems in the country. Despite this, when he got the shot, “there was no paperwork, there was no asking my history, there was no consent form, there was no anything,” he said.

About a week later, Wallskog’s feet became numb. Then he started getting “electrical sensations” down his legs when he bent his head forward. He compared the sensation to “putting your finger in an outlet.”

When he began having trouble standing, he ordered emergent MRIs and was found to have a lesion on his spinal cord.

A neurologist diagnosed transverse myelitis, a disorder caused by inflammation of the spinal cord. Myelin is the protective covering over the nerves, and without it, electrical impulses are not transmitted correctly, resulting in loss of feeling and mobility.

Wallskog noted that he was quickly diagnosed because he is a physician. “Being in the healthcare system, I can navigate the system like not many people can,” he said.

“That’s why I’m worried about so many [other people’s] injuries that are going to take months to get worked up. If the providers don’t know what to look for, [others] will maybe never get a diagnosis.”

Despite various treatments and rest, Wallskog suffers pain and numbness and is unable to stand long enough to perform surgery. His career came to an end in early 2021.

‘Look at the data yourself’

Wallskog said he is now embarrassed for his profession.

“I feel like I’ve been unblinded …  like I got off the hamster wheel and I stopped drinking the Kool-Aid and I started asking questions,” he said. “I started looking. I started talking to people.”

“Look at the data yourself,” he advised. “Don’t wait for the media, who will twist every data point.”

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Despite what we’ve been told for more than two years now, “science is a dynamic process,” he said:

“Science isn’t settled. Science is a process of exploration, of admitting when you’re wrong, finding out what you’re right on. You have hypotheses, you test them … move forward. And people need to realize that and not necessarily trust these people that are so-called experts.

“I am open to learning and seeing the truth. If there are things that I’m wrong [about], that’s fine, that’s part of science.”

“I’m so thankful that you’re saying this,” Locricchio told Wallskog. “Because it really means something … you’re a citizen, you’re an injured person, but you’re also a physician.”

Wallskog has now taken matters into his own hands in an effort to help others. “We’re sick and tired of waiting for other people to do the right thing,” he said. “We’re just going to do it ourselves.”

He is now co-chairman, along with Brianne Dressen, of REACT19, a “science-based nonprofit” offering financial, physical and emotional support for those suffering from long-term COVID-19 vaccine adverse events.

The REACT19 website states:

“​​React19 works with both patients and providers as well as research teams. Our programs all fall within our 3 categories of assistance (financial, physical, and emotional).

“Programs include funding, promoting, and sharing relevant scientific research; bringing the right medical teams together with patients; direct financial assistance; educational outreach; and supporting communities where impacted people can begin to heal physically and emotionally.”

Financial support is important, said Wallskog, but acknowledgment of vaccine injuries is just as vital.

He spoke with Dr. Peter Marks, director of the Center for Biologics Evaluation and Research (CBER) at the U.S. Food and Drug Administration. According to Wallskog, “[Marks] privately said, ‘I acknowledge these injuries,’ but he won’t publicly acknowledge them.”

“This was a quote on video,” said Wallskog. “And I said, ‘well, that’s too bad because acknowledgment is important.’”

Wallskog added:

“Without the [Centers for Disease Control and Prevention], the [U.S. Food and Drug Administration], the [National Institutes of Health] and other governmental agencies acknowledging these injuries, the conditions won’t be communicated to the healthcare community. If the healthcare community doesn’t know what to look for … when these people present [to a doctor with symptoms], then they’re just gaslit.

“Acknowledgment leads to the development of evaluation and treatment protocols for these people. That’s why it’s important … And the other thing is to support these people. And that’s what I’m hoping to do through REACT.”

https://childrenshealthdefense.org/defender/covid-vaccine-injury-ends-surgeons-career/

Citizens’ Log – May 10 – How the fall of human civilization was pulled off through the deliberate destruction of the PHYSICAL infrastructure that keeps humanity alive 05/10/2022 / By Mike Adams

Today’s Citizens’ Log podcast – formerly known as Situation Update – reveals how globalists achieved the fall of human civilization by dismantling the physical infrastructure that once kept humanity alive.

Citizens’ Log is recorded and preserved for future historians in the hopes they might study the mistakes that lead to the fall of human civilization. Each episode reports on present-day events that are leading to the cultural collapse, food collapse, economic collapse, cognitive collapse and infrastructure collapse… all headed toward the grand finale civilization collapse which will end this era of madness and lead to a “global reset” / mass die-off.

We anticipate that, at minimum, 2-4 billion people will be killed over the next decade due to vaccine damage, vaccine-induced cancer deaths, starvation, economic collapse, lawless violence and World War III events (which will likely include EMP weapons or nuclear weapons). If the USA continues to push Russia into nuclear escalations, that number could easily rise to 4+ billion human casualties.

Globalists are trying to exterminate 7.5 billion.

The “Climate Change” excuse to dismantle the infrastructure that feeds the world

What’s clear is that the criminal cabal currently running the world is meticulously working to exterminate the human race — a kind of planetary-scale “ethnic cleansing.” The excuse they’ve come up with is “climate change” – a delusional fairy tale that claims carbon dioxide kills plants (it actually does exactly the opposite) and that a colder planet Earth would be “greener” (again, it’s exactly the opposite of reality).

Under the camouflage of “climate change,” the world’s Western nations have dismantled their energy infrastructure, shutting down pipelines, halting drilling, punishing coal miners and waging economic warfare on the entire energy infrastructure. As the collapse accelerates, the globalists order people to, “Go green!” but offer no practical way to actually transition from oil to anything else.

The “Go green” cheer is really just a virtue signaling way to say, “Go F off and die.”

It was never about “going green,” you see. It was always about extermination of the human race. And without the energy infrastructure that provides fertilizer, farming and food transportation, at minimum half the world’s population would starve to death. This was, of course, precisely the plan.

Now the world faces engineered mass starvation and economic collapse

The deliberate dismantling of the infrastructure that keeps civilization functioning is now leading directly into mass starvation and economic collapse. This will only be exacerbated by the currency collapse that’s about to be sprung on the world, leading to a rapid, global collapse of the world’s dominant fiat currencies.

In our estimation, the Euro will likely collapse in the next year, and the Yen won’t be far behind. The US dollar is on its way out and is facing a global repudiation scenario where 100+ countries simultaneously denounce and abandon the dollar, leading to a near-instant wipeout of dollar-denominated assets, followed by the collapse of the US government empire.

The collapse of the dollar will lead to widespread civil unrest and violence across America. The inability to print new money that has any value will see the entire criminal cabal in Washington D.C. implode, unable to keep their fraudulent printing presses running (such as the now-$40 billion “support” package designated for Ukraine, most of which will end up in the pockets of corrupt US officials and their family members).

On one hand, an observer might see the downfall of the criminal cabal in D.C. as a good thing, but as that happens, the American people will be facing chaos, starvation and violence in their own cities and towns. Order will slowly be restored as states secede from the union and declare their own local currencies, reestablishing trade and transactional infrastructure for commerce.

See my free downloadable audio book, “The Global Reset Survival Guide” to learn how to make it through what’s coming.

The CEO of Scottish Power warns 10 million UK households won’t be able to afford to heat their homes this winter

Due to the deliberate shutdown of Western Europe’s fossil fuels infrastructure, 10 million UK homes won’t be able to afford to heat their homes this winter, according to Scottish Power CEO Keith Anderson. The BBC reported:

Keith Anderson, chief executive of Scottish Power, told the BBC that another expected rise in energy bills in October to between £2,500 and £3,000 a year could see huge losses for suppliers and many customers unable to pay their bills.

“We need to be realistic about the gravity of the situation – around 40% of UK households, potentially 10 million homes, could be in fuel poverty this winter,” Mr Anderson explained.

Mr Anderson also said more energy companies could collapse if their customers were unable to pay their bills.

RT.com (Russia Today) also covered the issue, attributing the following quote to Anderson:

“If nothing else happens by October, I think we will see a huge increase in pre-payment customers in effect self disconnecting – not reloading their pre-payment meter because they can’t afford to do it.”

“We will also see a massive increase in debt levels for direct debit customers, and a massive increase in people being pushed from direct debits to prepayment meters so that companies can recover the debt,” he continued. “We are heading to a really horrible place where none of us want to be.”

Since that reporting, Kiev has reportedly shut off one-third of all Russian natural gas headed for Western Europe, citing a force majeure emergency and claiming gas can no longer flow.

This means one-third of the natural gas to Europe was just cut off in one day. The ramifications of this have not yet hit the financial markets. Once they do, Europe will be in an outright panic.

Today’s Citizens’ Log covers all this in more detail, and expands to additional news items such as the accelerating collapse of financial markets and the implosion of crypto values. Catch it here:

Brighteon.com/b9f0b066-f5e3-4441-a20d-c3a720d63cb5

Witness the girl-maiming SCAR CULT being pushed by Biden and leftists who encourage young girls to have their breasts sliced off with medical scalpels Monday, May 09, 2022 by: Ethan Huff

(Natural News) Girls as young as 13 are increasingly opting to slice off their breasts as part of an LGBT push to turn more American children into transgenders. And the Biden regime is largely to blame for this horrific trend.

Thanks to years of grooming at government-run public schools, American kids today are less concerned about enjoying their innocence and more focused on cutting off their genitals and taking gender-bending pharmaceuticals in order to join the ranks of the “rainbow” cult.

On their own, innocent children would never dream up perversions like this. Evil adults, many of them demon-possessed, are the ones responsible for turning the United States into Sodom and Gomorrah – and their demonic work has only just begun.

The below video from The Western Journal explains how the Biden regime (meaning the Obama regime, since Barack appears to be the one truly running things) is largely responsible for the trans-ification of America into a nation of Baphomets:

Since 2017, the percentage of Americans teens wanting to become transgenders has more than doubled

School curriculum, media programming, government messaging, and corporate propaganda are all contributing factors as well to the swift decline of America’s youth.

The end result of all this grooming is confusion, followed by pressure and even a desire to follow the script straight into “transitioning,” which is what increasingly more children these days are doing.

In 2017 when Donald Trump first became president, only about three or four out of every 100 American teens expressed interest in becoming transgender. By 2021, that number had more than doubled to nine in 100 children.

One can only imagine what the figure is currently as things accelerate exponentially.

“These children have been groomed to believe the idea that if they don’t feel quite right socially, if they don’t fit in for one reason or another, they might be trapped in the wrong body,” writes Michael Austin for The Western Journal.

“Because of this, many kids who suddenly identify as trans are experiencing social awkwardness, going through puberty and/or suffering from social development disorders such as autism and ADHD.”

It is perfectly normal for young people to experience confusion about who they are as they develop from childhood into puberty. What is not normal is them having perverse adults all around trying to convince them that this points to transgenderism.

“These children are being groomed to believe that the normal stresses of childhood can be solved through gender transitioning,” Austin adds. “They’re told that if you don’t feel right in your own body, the only way to feel whole is to mutilate that body to better fit the opposite gender.”

The Biden regime and leftists call this “gender-affirming care,” but nothing could be further than the truth. Instead of affirming children in their natural-born genders, perverse adults are telling them that they must affirm a different gender than the one that matches their anatomy.

Again, this is called grooming, and the Bible warns that people who engage in such are better off having a millstone tied to their neck and getting tossed into the ocean, as opposed to the judgment they will face at the hands of an angry God.

“Children need to learn how to tie their shoes and they need to be taught about math and reading, not the strange sexual ideologies of political activists,” Austin says.

“If you disagree, if you believe this sort of political and sexual grooming should be permitted in a classroom full of young children, there’s only one thing left to say: OK, groomer.”

The latest news about America’s rapid decline into the depths of hell can be found at Collapse.news.

Sources include:

WesternJournal.com

NaturalNews.com

BlueLetterBible.org

Life insurance company says death claims up 40% after covid vaccines Monday, January 03, 2022 by: Ethan Huff

(Natural News) The OneAmerica insurance company is reporting a major uptick in death claims ever since Wuhan coronavirus (Covid-19) vaccines were introduced under Operation Warp Speed.

The Indianapolis-based company, which has been around since 1877, says that the death rate is up 40 percent compared to pre-plandemic levels. And these deaths are occurring in working-age people, just to be clear, between the ages of 18 and 64.

“We are seeing, right now, the highest death rates we have seen in the history of this business – not just at OneAmerica,” confirmed company CEO Scott Davison about this industry-wide trend.

“The data is consistent across every player in that business.”

Dr. Robert Malone, M.D., M.S., the inventor of the mRNA (messenger) technology used in Fauci Flu shots, says he was shocked to receive an email about OneAmerica’s announcement from a stock analyst colleague of his.

“This headline is a nuclear truth bomb masquerading as an insurance agent’s dry manila envelope full of actuarial tables,” Malone writes, pointing to the headline that stated:

“Indiana life insurance CEO says deaths are up 40% among people ages 18-64”.

Big Pharma working with Big Tech to cover up 100,000 excess deaths per MONTH from covid jabs

Up until now, Malone has taken a more conservative approach to the plandemic. He knew for a while that the jabs were a bad idea, but he stopped short of calling the whole thing a conspiracy.

All of that quickly changed, however, after Malone got banned from Twitter simply for telling the truth.

After losing access to his more than 500,000 followers, Malone came to the shocking realization that this is not only a conspiracy but one that involves more than just Big Pharma. Big Tech is also involved, and is working overtime to cover up the fact that nearly 100,000 excess deaths are now occurring per month, thanks to the injections.

Be sure to also check out the following “Situation Update” with Mike Adams, the Health Ranger, who dives deep into the scandal from his own unique perspective:

Malone agrees that we need another round of Nuremberg trials

Malone describes his journey of being “red-pilled” as an adventurous one, to say the least. He now understands that there is, in fact, a “Great Reset” depopulation plan in action, and that the jabs play a big role in this.

He also now understands why Reiner Fuellmich is pushing for another convention of nations to try and prosecute those perpetrating this mass genocide against the people of the world.

There is simply no denying anymore that all-cause mortality is off the charts. And the only thing that has changed, besides the alleged “spread of covid,” is mass vaccination with mystery chemicals, one of which (mRNA) Malone himself created.

The general consensus seems to be that the cause of this spike remains a “mystery.” But again, the only thing that has changed is that tens of millions (billions?) of people have had their genes and immune systems tampered with by Big Pharma and the government.

After reading the entire announcement from OneAmerica, Malone concluded that, at a minimum, the nation now has “both a huge human tragedy and a profound public policy failure” on its hands.

“IF this holds true, then the genetic vaccines so aggressively promoted have failed, and the clear federal campaign to prevent early treatment with lifesaving drugs has contributed to a massive, avoidable loss of life,” he adds.

The Biden regime also has a whole lot of blood on its hands for mandating these things on workers and others, which represents a serious crime against humanity and a massive loss of life.

“FURTHERMORE, we have also been living through the most massive, globally coordinated propaganda and censorship campaign in the history of the human race,” Malone further writes, pointing to Big Tech platforms like Twitter for their complicity.

“All major mass media and the social media technology companies have coordinated to stifle and suppress any discussion of the risks of the genetic vaccines AND / OR alternative early treatments.”

Malone is particularly incensed that the First Amendment to the United States Constitution has been systematically erased by the likes of Twitter (and Facebook / Meta and many others).

“We are not just talking about running over the first amendment of the Constitution of the United States and grinding it into the mud with an army of artificial intelligence-powered heavy infantry,” he says.

“This article (by OneAmerica) reads like a dry description of an avoidable mass casualty event caused by a mandated experimental medical procedure. One for which all opportunities for the victims to have become self-informed about the potential risks have been methodically erased from both the internet and public awareness by an international corrupt cabal operating under the flag of the ‘Trusted News Initiative.’”

The latest news about Chinese Virus injections can be found at ChemicalViolence.com.

Sources for this article include:

TheCenterSquare.com

RWMaloneMD.substack.com

NaturalNews.com

Brighteon.com

Australia’s Record COVID-19 Death Count Mounts Yet Politicians Act Like Everything Normal

The heavily vaccinated Australian population continues to struggle with record surges of deaths associated with the novel coronavirus. But how could that be the case with nearly the entire population vaccinated? While the COVID-19 vaccines do not stop infection nor viral transmission, they have been shown to at least, reduce serious disease and death. Yet as TrialSite has chronicled, in heavily vaccinated nations from South Korea to New Zealand and Australia, the deaths associated with COVID-19 continue to soar. Now, the mainstream press in Australia acknowledges the growing breakthrough COVID—19 hospitalizations and death toll yet doesn’t raise any critical questions.

As covered in the Sydney Morning Herald, COVID-19 related deaths have hit 7,495 based on health department data. As TrialSite reported, in the first months of 2022 (now four), more than double as many persons have died than during all of 2020 and 2021 combined. That’s right: 5,269 Australians have died since January 1, 2022, out of the total 7,495.  With little media attention anywhere else, COVID-19 went from the 38th leading cause of death in 2020 to the second next to cancer by January 2022, based on a review of statistics from the Australian Board of Statistics, report Chloe Booker and Najma Sambul.

Who is dying from COVID-19? According to the recent media entry, over 75% of the deaths are the elderly, aged 70 and up, but the deaths also include eight children under the age of 9, as well as 5 children to adolescents aged 10 to 19. 30 persons in their 20s have died.

In the meantime, TrialSite reports that about 84% of the entire population has been fully vaccinated with about 52.5% of the population having received at least a third booster shot.

Australia’s Therapeutic Goods Administration (TGA) approved four vaccines including Pfizer-BioNTech- was approved on January 25, 2021, then the AstraZeneca-Oxford on February 16, 2022, along with the Janssen approved June 25, 2021, and then Moderna 9 on August 9th.

Politicians are Deadly?

TrialSite spoke with a few subscribers in Australia who report that the general messages coming out of the mass media and government avoid any discussion of waning vaccine effectiveness, especially in the elderly other than its time for a booster shot for those that haven’t received one.

Waning vaccine efficacy against the Omicron variant of concern represents a dangerous situation, especially for the elderly.

Yet with a forthcoming election political parties seem to want to appeal to the good side of the masses, campaigning on the joys of newfound freedom—time to drop the masks and the like. This, despite record surges of COVID-19 infections, near record hospitalizations, and crushing record-breaking mortality rates. 

As reported in the Sydney Morning Herald, at least some academics are calling out the politicians like Professor Nancy Baxter with the University of Melbourne, School of Population and Global Health who shared that both political parties run campaigns now as if COVID-19 doesn’t even exist—at a time when death rates shatter all records!

Professor Baxter said, “[It’s the] the biggest medical emergency or challenge that we’ve ever faced, and continue to face, and yet you hear nothing,” she said. “There’s no actual meaningful discussion or debate around management of the pandemic.”

She pointed to Victoria, noting Premier Daniel Andrews, up for election in November, doesn’t want to be associated with COVID-19 restrictions (e.g., masks, lockdowns, etc.).

Yet Professor Baxter herself doesn’t dare question the efficacy of the current mass vaccination regimen in place, rather sharing that what is needed is more childhood vaccination and boosters for the remaining elderly that haven’t yet been vaccinated.

This very well could help in the short run, but what explains the growing death rates of fully vaccinated and boosted persons? Most of the elderly are now boosted, yet 75%+ of the deaths fall in this cohort.

Australians don’t want to go back to restrictions, and politicians are pretending that COVID-19 barely exists while the public health agencies simply push vaccination with the same increasingly questionable products as the answer. In the meantime, the actual data points to a worsening health crisis.

References