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Jerm Warfare Interviews Denis Rancourt – 31 Millions Deaths from Covid Vaccine & Covid Policies

Etienne de la Boetie2 | August 21, 2024

Award-winning South African political cartoonist and talk show host Jeremy “Jerm” Nell interviews world-class academic Denis Rancourt (h-index 41 & i10 index of 91) on his latest paper showing an estimated 31 million dead from the Covid “vaccines” and the government’s Covid policies. We have a summary of the interview and full transcript at https://artofliberty.substack.com/p/dr-denis-rancourt-31-million-dead

August 24, 2024 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, Video, War Crimes | , , , | Leave a comment

Australian Government blocks Covid inquiry ‘with teeth’

Once again, Labor characterised its foes as ‘conspiracy theorists’, ‘cranks,’ ‘kooks’ and ‘far right extremists’ rather than engaging in rational debate

By Rebekah Barnett | Dystopian Down Under | August 22, 2024

The Australian Government has voted down a bill to establish a Covid Commission of Inquiry, which would have essentially the same powers and independence as a Royal Commission.

The bill was supported by a small coalition of senators from minor parties and the Opposition (conservative), but was rejected by the Labor Party(left-wing) in a vote today.

To date, Australia has had plenty of Covid inquiries, but none with teeth.

The siloing of inquiries to deal only with states and territory and federal governments on an individual basis has allowed for a lot of finger pointing with very limited accountability.

The scope of the federal Covid Inquiry excludes the policies of state and territory governments, which enacted vaccine mandates, lockdowns and inter-state border restrictions, leading politicians and media to call it “toothless.”

In turn, states and territories have focused on how well they implemented policies heavily influenced by the Federal Government and national advisory bodies without actually considering whether the policies were any good.

The patchwork nature of these inquiries allows the Federal Government to blame states and territories for implementing the harshest measures, and the states and territory governments pass the buck to the federal agencies and departments for influencing them to do so.

More holistic independent reviews like the Fault Lines report have resulted in talk of ‘lessons learned’ about “ill-conceived policies, politically driven health orders and excessive use of lockdowns,” but no meaningful attempts to hold anyone to account or guarantees that the lessons will inform future pandemic policy making.

Another problem with inquiries to date is that federal, state and territory governments have played hide the ball with important documentation and data required to properly assess their performance. As yet, no Australian government has released the health advice that draconian measures were based upon.

A Royal Commission or similar, taking the entire Covid response – at federal, state and territory levels – and with aggressive powers to command access to information that governments don’t want to release, would be required for real accountability.

The only ways to bring this about are for the executive to call a Royal Commission, or for the Senate to call a Commission of Inquiry.

However, despite the recommendation of the Senate Select Committee on COVID-19 in 2022 that a Royal Commission into Australia’s Covid response be established, the Labor Government has resisted calls to do so.

The Committee, led by senior Labor Party member Katy Gallagher (now Minister for Finance, for Women and for the Public Service) criticised the then Liberal Government’s lack of transparency and accountability around pandemic decision making by the National Cabinet.

Emergency law making had “challenged the Australian Parliament’s capacity to provide meaningful scrutiny of proposed laws, particularly in identifying and addressing the impact of emergency powers on the rights of individuals,” the Committee stated in its recommendations.

Leader of the Opposition at the time, Anthony Albanese, sort of promised a Covid Royal Commission. But after being elected to government in May 2022, Prime Minister Albanese has resolutely dodged the issue, throwing his support behind the limited federal inquiry instead.

Hence, a group of concerned senators tabled the COVID-19 Response Commission of Inquiry Bill 2024 in a bid to open up option B, an inquiry initiated by the Senate.

The bill, prepared by Senator Matt Canavan (Liberal), was co-sponsored by Senators Malcolm Roberts (One Nation), Alex Antic (Liberal), Gerard Rennick (Liberal), Ralph Babet (United Australia Party) and Matt O’Sullivan (Liberal), all of whom have been vocal critics of Australia’s pandemic response.

Source: Senator Alex Antic on X

During speaking time, senators who sponsored the bill argued that a Covid Commission of Inquiry is needed so that Australia can finally move on from Covid with a good plan in place for future pandemics. A proper inquiry would get to the bottom of what went wrong (and what went right) to restore trust in public health, they said.

Senator Roberts also said that in light of the fact that multiple U.S. states are now suing Pfizer for misleading about its Covid vaccine, if an inquiry found that Pfizer was indeed guilty of fraudulent behaviour, this could shift the financial burden of injuries and deaths associated with Pfizer’s product from Australian tax payers to the pharmaceutical giant.

Australian tax payers have coughed up more than $20 million on compensation for Covid vaccine injuries, but they will have to pay a lot more if a Covid vaccine injury class action is successful. The action, which was filed in the Federal Court last year, has enrolled over 1,500 injured Australians (or families of the deceased).

However, only ten senators supported the bill when it went to a vote in Parliament today. The bill was supported by the above mentioned senators (with the exception of Senator Antic, who is on leave), some members of the Coalition, One Nation, and independent Senator David Pocock.

Despite Greens Senator Jordon Steele-John stating that his party supports the establishment of a “frank” and “transparent” inquiry with the powers of a Royal Commission, the Greens abstained from the vote. Labor voted against the bill.

Source: Dynamic Red, 22 August 2024

I am told by the office of one of the senators who sponsored this bill that they have no intention of dropping the matter.

Previously, Senator Babet brought five separate motions to establish the world’s first government Excess Mortality Inquiry, which is now in progress thanks to Senator Babet’s persistence.

An inquiry into proposed terms of reference for a Covid Royal Commission has already been conducted, which will prove helpful in the event that either a Royal Commission or a Commission of Inquiry into Australia’s Covid response are eventually established.

Nonetheless, such efforts will face stiff opposition from the Albanese Government, if Labor Senator Tim Ayres’ speech in Parliament today is representative of his party’s position.

In speaking time before the vote, Senator Ayres said that the Government did not support the bill because “there’s already a public inquiry,” before launching into an astonishing diatribe of ad hominem attacks on the senators who proposed the bill.

Senator Ayres used the term ‘conspiracy theories’ or ‘conspiracy theorist’ more than twenty times, likened the efforts of senators to bring about a thorough Covid inquiry to movements motivated by “anti-semitism,” and called these same senators “cranks,” and the “nastiest, extreme, kooky elements of politics.”

Senator Ayres referred to ‘conspiracy theorists/theories’ more than 20 times in Parliament, 22 August 2024. Source: Australian Parliament House Streaming Portal, YouTube.

Senator Rennick called Senator Ayres’ speech “disgusting,” stating, “all we’re recommending today and supporting is that we have a thorough inquiry.”

In a statement after the vote, Senator Canavan said that more disheartening than Australia’s damaging pandemic response was “the response to the response.”

“Those Australians hurt during Covid deserve to have the accountability of proper public hearings, the publication of all the health advice and an open, transparent attempt to recognise mistakes as well as put in processes to prevent such things ever happening again.

“Why can’t the Government accept that if it is given immense power to lock people in their homes and force people out of work, that there should be an equal and corresponding obligation for them to be accountable to the people hurt by their decisions?”

Senator Babet took to X to express his dissatisfaction with the outcome, calling the decision of the Senate “weak.”

“Is it too much for Australians to ask for governments and the bureaucrats advising them to be held to account for the advice and actions they took during the pandemic?”

Apparently, yes.

August 24, 2024 Posted by | Civil Liberties, Science and Pseudo-Science, Timeless or most popular | , , , | Leave a comment

Categorizing The mRNA-Vaccinated… Most Can Be Forgiven, But Some Cannot

By P Gosselin | No Tricks Zone | August 24, 2024

When discussing the mRNA COVID vaccines, we need to be careful about dividing people into the two broad groups of the vaccinated and the unvaccinated.

The truth is that many vaccinated people didn’t want to be injected and now deeply regret it.

There are 6 categories of the vaccinated, ranging from the innocent victims to the wicked, unrepentant perpetrators.

1. Those vaccinated by force, against their will
These people were forced to get the jab against their will, and included babies and children who were unable to resist. By forced, we mean they were subjected to extreme duress through threats like job loss or being banned from performing their livelihoods. Many knew that the experimental mRNA shots were potentially dangerous, or didn’t work, and were just unnecessary, but were forced against their will to accept them. These people are victims serious human rights violations. – injured or not.

2. The harassed and coerced
These people were not convinced and many were distrustful of the shot, or even fearful of the drug’s side effects. Many understood that the novel gene-manipulative drug was untested and could be potentially dangerous. Many understood the risk,and never would have allowed themselves to be vaccinated. But they did because the harassment at work, home and in public was just too much to bear.

3. The restriction dodgers
Many were convinced the novel vaccine would work or at least wouldn’t do any harm. Many had felt they didn’t need it, but simply wanted to go back to normal living. Unfortunately these people didn’t do the necessary research to make an informed decision. They were duped into thinking they weren’t harmful. We can forgive this category because at least they didn’t run around lecturing, persecuting and excluding those who resisted taking the mRNA shots. Like in category 1 and 2 above, many deeply regret allowing the injection and promise not to ever take these shots again.

4. The dimwitted follower sheep
They were gullible beyond belief, blindly following everything they were told, and refused to listen to informed experts and hard data contradicting the bogus claims made by the vaccine makers and tyrants. Even today many continue to insist the vaccine works, some even willing to roll up their sleeves again whenever instructed. Too many of them are simply too brainwashed, hypnotized are just flat out too dimwitted to learn. For them, denying is better than confessing and admitting to having been a fool. Yet, we can forgive them to some extent, but we need not give them much sympathy if things go wrong for them.

5. The mRNA vaccine tyrants
We all know who these people are. They were in the media, institutes, governments and big corporations. They lied and hid the risks from us. These people will remain evil until they confess to their grave sins and change their malicious ways. Everyday we heard them ridicule, persecute, marginalize and coerce the unvaccinated. Many of these tyrants need to be punished, prosecuted for fraud, or forever fired from their positions. The late Dr. Vladimir Zelenko even called for the death penalty for the worst offenders. These people can be forgiven, but only through lots of repentance, remorse, apologies and making solemn pledges to redeem themselves.

6. The unrepentant mRNA tyrants
Those who don’t repent must know we will never forget and will not ever relent hauling you in to face legal justice. Your numbers are shrinking and your protection is crumbling. But it’s (still) not too late for you to redeem yourselves.

August 24, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular, War Crimes | | Leave a comment

Mpox ‘Not the New COVID’ — But Vaccines Still The Answer, WHO Claims

By Suzanne Burdick, Ph.D. | The Defender | August 21, 2024

Mpox is “not the new Covid” — but vaccines are needed to stop the spread, according to the World Health Organization (WHO).

Hans Kluge, WHO regional director for Europe, emphasized in an Aug. 20 media briefing that, unlike COVID-19, mpox primarily spreads through close skin-to-skin contact with mpox lesions.

Referring to mpox as a “test for global equity,” Kluge urged European countries to “act in solidarity” with African countries by taking measures — such as vaccination, surveillance and administering antiviral drugs — to control the disease.

“We can, and must, tackle mpox together — across regions and continents,” he said.

Dr. David Bell, a public health physician and biotech consultant, told The Defender the WHO’s response to the recent mpox outbreak is more about producing profits than addressing global health disparities. “This is about selling more stuff, not health equity,” he said.

The number of deaths caused by mpox is minuscule compared to the number of deaths caused by other diseases common to Africa, such as tuberculosis and malaria.

“Although the actual numbers are unclear,” Bell said, “WHO claims about 500 deaths from Mpox this year in DRC [Democratic Republic of Congo]. That is about how many people die of tuberculosis every 4 hours.”

The DRC, which is about the size of Western Europe and is home to roughly 110 million people, is regarded by the World Bank as one of the world’s poorest countries.

By overly focusing on mpox, Bell explained, the WHO is diverting funding from addressing these other diseases and “very basic” issues affecting DRC residents’ health, such as sanitation and nutrition.

Journalist James Roguski pointed out that the South Africa Vaccine Injury Medico-Legal Study-Group doesn’t support the emergency rollout of a mpox vaccine.

Roguski told The Defender, “Clearly, there are far more serious health issues in the DRC than the 500+ deaths attributed to mpox.”

Roguski said the WHO’s method of counting cases of mpox is “blatantly fraudulent.”

“The WHO defines a ‘confirmed case’ of mpox as anyone with a positive result on a PCR ‘test,’” he said. “The PCR process is NOT capable of diagnosing disease. It is also NOT capable of identifying an intact virion that might be transmissible or contagious.”

Nonetheless, South Africa President Cyril Ramaphosa — who leads pandemic preparedness activities for the African Union — on Aug. 17 called on countries in the region to allocate more domestic funds to fight mpox, according to the African Centres for Disease Control and Prevention (CDC).

Mpox vaccine makers rev up production 

The African CDC announced it is enacting a “clear plan” to get 10 million doses of vaccine for the continent after the WHO’s Aug. 14 declaration of mpox as a global public health emergency, reported the BBC.

Vaccine maker Emergent BioSolutions on Aug. 19 responded to the WHO’s declaration by pledging to donate 50,000 doses of its smallpox vaccine to African countries. The company in 2023 submitted its smallpox vaccine, ACAM2000, to the U.S. Food and Drug Administration (FDA) for approval for immunization against mpox.

Joe Papa, Emergent’s president and CEO, said the company for years has supplied the vaccine to the U.S. and “allied governments in support of preparedness and stockpiling initiatives.”

“Currently,” Papa said, “we have additional product already in inventory, with the ability to increase supply by approximately 40 million doses, if and potentially when needed.”

The U.S. and Japan also recently pledged to donate vaccines to DRC, Reuters reported.

Bavarian Nordic — manufacturer of the Jynneos vaccine — said in an Aug. 17 statement that it is working closely with stakeholders to provide “equitable access” to its mpox vaccine in Europe and beyond.

“We are also working with the WHO on a regulatory path to ensure access to all countries,” said Bavarian Nordic CEO Paul Chaplin.

Jynneos vaccine can cause heart problems 

On Aug. 16, Bavarian Nordic said it plans to seek European regulatory approval for its Jynneos vaccine for children ages 12-17. The FDA granted the vaccine an “emergency use authorization” for adolescents during the 2022 global mpox outbreak.

Roguski pointed out the Jynneos vaccine was shown by the FDA to cause severe cardiac adverse events in 1.3% of recipients. He said it was “absolutely unacceptable” that the vaccine be recommended for use in adults or teens.

Dutch attorney Meike Terhorst — who has called out the WHO for its “powergrab” in Europe via its revised International Health Regulations — told The Defender the WHO’s actions in Europe and Africa need to be “critically followed.”

“It is important that medicine does not transform into medical tyranny,” Terhorst said.

Bell — who formerly served as a medical officer and scientist at the WHO — said the WHO in past years wasn’t so intensely focused on applying pharmaceutical solutions to global health problems.

“What we are witnessing,” Bell said, “is an acceleration of the pivot of international public health from major health burdens and basic improvement of metabolic and health resilience, such as sanitation, nutrition and living conditions — the major influences on longevity in wealthy countries over the past 150 years — to dramatization of anything that can be heavily commoditized.”

Although pharmaceutical products may sometimes play a role in improving health equity, the improvement in basic living standards, in supply lines for basic health essentials and in strengthening economics are “overwhelmingly the most important.”

“Most people working in international public health are fully aware of this, but we have now built an industry where all the incentives are to please funders linked to the pharmaceutical industry — whilst the role of the pharmaceutical industry’s leaders is to maximize profits for themselves and their shareholders,” Bell said.

The people in central Africa will, unfortunately, come out worst off, he said. “Before blaming Pharma, we should blame ourselves for allowing such an industry to be built.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 24, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular | , | Leave a comment

CDC USES ‘COVID SURGE’ TO STOKE FEAR

The HighWire with Del Bigtree | August 22, 2024

The CDC is using new, questionable techniques to declare a ‘COVID surge’ and stoke fears. Coincidentally, a new booster hits the market as students head back to school. Jefferey Jaxen reports.

August 23, 2024 Posted by | Science and Pseudo-Science, Video | , , | Leave a comment

Statement on proposed emergency roll-out of vaccine program in Africa for monkeypox

SAVIMS | August 23, 2024

We are deeply concerned about the recent announcements made by Africa Centres for Disease Control and Prevention (CDC) Director General Jean Kaseya on Aug. 13 and World Health Organization (WHO) Director-General Tedros Adhanom Ghebreyesus on Aug. 14. It is important to address these announcements openly to the public.

In his statements, Kaseya declared regarding monkeypox vaccines:

“We have a clear plan to secure more than 10 million doses in Africa, starting with 3 million doses in 2024.”

We at the South Africa Vaccine Injury Medico-Legal Study-Group (SAVIMS) would like to point out pertinent facts to both institutions and other relevant bodies of interest:

1. There is no prescribed vaccine with documented Level 1 scientific evidence for monkeypox. The current WHO-recommended live virus vaccines, Jynneos and ACAM2000, are:

(a) intended for smallpox and are thus experimental for monkeypox;

(b) have reported serious adverse effects, and;

(c) contain live viral strains which may instigate a resurgence of the eradicated smallpox virus.

2. The potential use of mRNA vaccines. There is no scientific evidence supporting the use of any mRNA vaccine to prevent or mitigate any infectious disease. The observed data of adverse reactions to experimental mRNA vaccines far outweighs any benefit.

3. Informed consent is an ethical concept that is codified in the law and is in daily practice at every healthcare institution. Three fundamental criteria are needed for clinical informed consent: the patient must be competent, adequately informed and not coerced.

It is not possible for any recipient of these vaccines to receive legitimate informed consent based on current research.

4. The article by Allan-Blitz et al., “A position statement on Mpox as a Sexually Transmitted Disease,” concluded that monkeypox is a “sexually transmitted disease.” Preventative measures for this scenario should necessitate and provoke relevant clinical and primary healthcare and education initiatives directed at the high-risk group.

There is no merit in the recommendation of experimental vaccines to the general population.

5. The statistics and analysis, regarding the collated monkeypox data in the Democratic Republic of Congo and other countries in Africa by the WHO, warrant further investigation and must be independently audited.

The areas in which the highest statistics were collated should detail the criteria for testing, the procedures for testing, equipment sensitivity and specificity, personnel skill, clinical scenarios, and provocation for testing these specific communities. What tests were done to investigate and exclude other diseases, including communicable diseases?

6. There have been no autopsy reports published on the deaths related to monkeypox. The lack of formal documented autopsy, lack of information regarding equipment test sensitivities and specificities, and lack of information on procedures validating random collation of data, further reduces and invalidates the authenticity of the statistics.

SAVIMS position statement regarding emergency monkeypox vaccine rollout in Africa

We have reviewed the literature and analyzed the data on monkeypox, as well as its etiopathogenesis. Based on our understanding of this disease:

1. We do not support the Africa CDC and WHO declaration of a global health emergency for monkeypox.

2. It is established that monkeypox is predominantly a self-limiting condition. This does not warrant vaccine intervention.

3. We strongly object, based on the scientific evidence, to the “emergency” rollout of repurposed smallpox vaccines or any other proposed monkeypox vaccine to the people of Africa.

4. We question the authenticity of the number of deaths associated with monkeypox, as reported by the Africa CDC unless it can be verified through autopsy.

5. We warn members of the public about the inherent risks of taking any vaccine, including those proposed for mpox, of which the effectiveness and safety have not been reliably determined by Level 1 clinical trials. There can be no justification for a vaccine with unknown adverse effects.

6. We urge the public to exercise their inherent human rights to refuse to give consent to any medical intervention that they do not feel comfortable taking.

We are open to dialogue and discussion with the Africa CDC on the issues raised above and on all matters of health and well-being concerning the African population.

SAVIMS is a voluntary multidisciplinary association under the Common Law governed by its members in accordance with the Constitution of the Republic of South Africa. The purpose of SAVIMS is to follow the evidence to gain and communicate knowledge about vaccine injuries. This knowledge is necessary for the treatment and counseling of patients with vaccine injuries; as well as for medico-legal report writing and provision of evidence in respect of victims of vaccine injury and in other vaccine-related disputes. The objectives of SAVIMS are to promote human health and human rights as enshrined in the Bill of Rights of South Africa’s Constitution.

August 23, 2024 Posted by | Science and Pseudo-Science | | Leave a comment

CDC Stands by Water Fluoridation After Report Linking Fluoride to Lower IQs in Kids Finally Published

By Brenda Baletti, Ph.D. | The Defender | August 22, 2024

The National Toxicology Program (NTP) on Wednesday published a controversial report linking fluoride exposure to neurotoxic effects in children, after public health officials tried for years to block its publication and water down its conclusions.

The report, which analyzed published studies on fluoride’s neurotoxicity, concluded with “moderate confidence” that higher levels of fluoride exposure in drinking water are consistently linked to lower IQs in kids.

It’s the first government publication to concede what fluoride researchers have long reported: that the chemical added to the drinking water of hundreds of millions of people in the U.S. and celebrated as one of the 10 greatest health achievements of the 20th century carries a serious risk of neurological damage, particularly for pregnant women and young children.

“The NTP monograph provides more than sufficient evidence against the deliberate exposure of humans to fluoride through intentional fluoridation of drinking water,” said risk analysis scientist Kathleen Thiessen, Ph.D., who was not involved with the study but co-authored the 2006 National Resource Council study on fluoride toxicity.

Thiessen told The Defender, “A conclusion of ‘moderate confidence’ of neurotoxic effects, especially on unborn and newborn children, ought to mean an immediate elimination of water fluoridation and minimization of fluoride exposure to the population.”

The report reviewed existing studies that assessed the relationship between fluoride exposure and neurodevelopmental effects in children and adults from across the world, including places where fluoride occurs naturally in groundwater and places like the U.S., Canada and Mexico, where it is intentionally added to drinking water or food.

The authors concluded that exposure to drinking water containing more than 1.5 milligrams per liter (mg/L) is consistently associated with lower IQ in children. That’s only twice the amount the Centers for Disease Control and Prevention (CDC) recommends be added to drinking water in the U.S. to prevent tooth decay.

Most environmental toxins regulated by the U.S. Environmental Protection Agency (EPA) are more strictly controlled. Typically, human exposure is banned at 30 times the level of their known toxic effects. None of the chemicals regulated under the Toxic Substances Control Act are permitted at a margin of less than 10.

The researchers found that almost all of the high-quality studies identified — 18 out of 19 — found a link between fluoride exposure and lower IQ in children. And 8 of 9 high-quality studies that looked at neurodevelopmental links other than IQ also found a link.

They said they were less confident that there was a consistent link between low levels of fluoride exposure in water and neurodevelopmental issues, and that more research is needed in that area. However, they also noted that water is not the only source of fluoride exposure.

“Additional exposures to fluoride from other sources would increase total fluoride exposure,” the report stated. “The moderate confidence conclusions may also be relevant to people living in optimally fluoridated areas of the United States depending on the extent of their additional exposures to fluoride from sources other than drinking water.”

Thiessen said pregnant women are often exposed to higher levels of fluoride because they drink much more water than others. And formula-fed infants are also at particularly high risk.

“While fluoridation of drinking water is the main source of fluoride intake for millions of people in the U.S., and probably the easiest to eliminate, it is not the only source of fluoride exposure, with toothpaste and tea probably being next in importance,” she said.

Fluoride advocates like the American Dental Association (ADA), the American Academy of Pediatrics (AAP) and the CDC argue that adding fluoride to water is an important public health practice because it prevents tooth decay by exposing teeth to low levels of fluoride throughout the day and strengthening teeth.

Federal health officials have been recommending water fluoridation for more than five decades. However, in the last several years as the NTP report has moved closer to publication, support for the practice has appeared to wane among some public health officials.

The U.S. surgeon general in 2015 officially lowered the recommended dosage for water fluoridation from 0.7-1.2 mg/L to 0.7 mg/L after considering adverse health effects. And in 2020, out of concern for the forthcoming findings in the NTP report, the U.S. surgeon general’s office declined to make a public statement endorsing the practice.

A spokesperson for the CDC told The Defender in a statement that the agency continues to support water fluoridation at current recommended levels.

“These recommendations are based on current scientific evidence and prioritize the safety, security, and health of all individuals,” the agency said. “Continued research is needed to better understand the health risks and benefits associated with low fluoride exposures.”

The spokesperson also said, “While concerns have been raised about potential risks associated with high fluoride exposure, it is important to note that these concerns are primarily based on studies conducted in countries with higher fluoride exposure than in the United States.”

However, some of the highest quality studies to date have been done in Canada and Mexico, where exposure levels were the same as exposure levels in parts of the U.S. And a paper published in JAMA Network Open in May found that children born to women exposed during pregnancy to fluoridated drinking water in Los Angeles were more likely to have neurobehavioural problems.

The ADA, AAP and EPA did not respond to The Defender’s request for comment.

The long road to publication

For more than two decades, researchers have drawn a link between fluoride exposure and neurodevelopmental issues. In 2006, the National Research Council of the National Academies of Science released a report on fluoride toxicity that identified serious health issues associated with fluoride exposure and called for further research.

The NTP, part of the U.S. Department of Health and Human Services (HHS) responsible for producing scientific research meant to inform policymaking, in 2016 began working on its review of fluoride’s neurotoxicity in humans.

After six years and multiple rounds of peer review, the NTP finalized its report in May 2022 — but public health officials within multiple agencies across HHS blocked its publication, according to emails obtained via a Freedom of Information Act request.

The NTP was compelled to send the report out for another round of peer review. Each round of peer review compelled the NTP to walk back some of its conclusions in what critics called an attempt to “delay it, to water it down.”

Former NTP director Dr. Brian Berridge told The Defender the report received unprecedented scrutiny because of challenges to the report by biased stakeholders. He said he believed it was an outcome of public health agencies’ desires to protect the practices they already have in place.

A draft version of the report was made public in March of 2023 under court order.

The order came as part of a lawsuit filed in 2017 by Food & Water Watch, Fluoride Action Network, Moms Against Fluoridation and other advocacy groups and individuals suing the EPA in a bid to force the agency to prohibit water fluoridation in the U.S. due to fluoride’s toxic effects on children’s developing brains.

After initial hearings in June 2020, presiding Judge Edward Chen placed the trial on hold pending the release of the report. After plaintiffs introduced evidence of agency attempts to suppress the report, Judge Chen ordered its release in draft form and the trial continued in January and February of this year.

The report, along with four major fluoride studies using birth cohorts — where researchers collect epidemiological data during pregnancy and then from children over their lifetimes to study a variety of health outcomes tied to environmental exposures — was key evidence in the trial.

The trial concluded on Feb. 13, and Judge Chen has not yet issued a decision.

The report finalized yesterday consists of one part of the NTP’s research. The other part, a meta-analysis, is forthcoming in a peer-reviewed journal.

NTP Director Rick Woychik said in a statement to The Defender that the delay in the report’s publication was due to an attempt to “get the science right” because “fluoride is such an important topic to the public and to public health officials.”

Woychik emphasized that water fluoridation “has been a successful public health initiative.”

Michael Connett, attorney for the plaintiffs in the case against the EPA, said the final version of the report, “confirms and actually further strengthens the NTP’s prior conclusions,” because the finalized version includes a supplemental review of more recent literature published between 2020 and 2023, which also finds a consistent link between fluoride exposure and adverse neurodevelopmental effects.

Connett added:

“Here you have an expert body of the US government confirming that fluoride is a neurotoxicant. That by itself is a very significant conclusion and should really prompt the question among policymakers and the public as to whether we really want to be adding a neurotoxicant to our water supply while questions remain about the precise doses that caused this effect.”

‘We didn’t sign up to add a neurotoxicant to our water’

The number of scientists and health professionals opposed to fluoridation has increased over the last several decades. Thiessen said the final publication of the monograph — and the forthcoming meta-analysis — provides important evidence for their position and might signal a change in the status quo public health position on fluoride.

“One hopes that it will help convince many more professionals that one of the 20th century’s top 10 public health achievements has in fact been terribly misguided from the beginning.”

The lawsuit brought public attention to the debate over water fluoridation ongoing among scientists working in public health for years, with many mainstream outlets addressing an issue that had often been disregarded as a conspiracy theory.

Connett said the government report ought to raise public concern and get more people asking questions about fluoridation. He said:

“This isn’t what people signed up for when we started adding fluoride to the water. We didn’t sign up to add a neurotoxicant to our water. We signed up for something that could help our teeth. Now that we know that it can affect their brain, we really need to go back to square one.”

Fluoride Action Network board member Rick North told The Defender that awareness about issues with water fluoridation has been growing for years.

“Fluoridation is a house of cards and it’s going to fall. It’s only a matter of when. The NTP report just made it sooner.” He said he hopes the final release of the report means a decision in the case against the EPA will come soon.

“For more than four years, Judge Edward Chen has waited for the final NTP report. Now he’s got it — even more scientific backing that fluoridation is an unreasonable risk to human health,” he said.

Stuart Cooper, Fluoride Action Network executive director, said the publication of the report was historic. “This report, along with the large body of published science, makes it abundantly clear that the question isn’t whether fluoridation is safe, but instead how many children have been needlessly harmed,” he said.

The report sometimes makes contradictory statements, Kim Blokker, a board member of Moms Against Fluoridation, told The Defender, showing the influence of the public health agencies on the reporting. “Do not be fooled by this attempt to muddy the waters of this otherwise definitive report, which contains more than enough evidence to prove the shockingly detrimental effects of fluoride exposure in young children.”

Kristie Lavelle, another board member of Moms Against Fluoridation, told The Defender they were happy to see the report finally published. “The time has come for fluoride to lose its status as a protected pollutant and to be treated the same as other recognized toxins such as lead and arsenic.”

With the publication of the report, she said, “We are one step closer to creating a world where clean water, air and food, and consequently vibrant health are the norm for our children and grandchildren.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 22, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular | , , | Leave a comment

Dr. Peter McCullough: COVID Shots for Kids ‘the Last Straw’

By Brenda Baletti, Ph.D. | The Defender | August 19, 2024

“A child today faces well over a hundred shots,” cardiologist Dr. Peter McCullough told host Mat Staver on a recent episode of “Freedom Alive.” Many of those shots are for infectious diseases of the past or contemporary illnesses that don’t pose a risk to infants.

McCullough said the “inflection point” was the 1986 National Childhood Vaccine Injury Act, which freed vaccine manufacturers from liability for vaccine injuries. “We saw essentially a vaccine bonanza develop,” he said, and “excessive, unnecessary” vaccination could be leading to serious side effects.

Those vaccines start just after a baby is born, he said, when they are given the hepatitis B vaccine.

As a cardiologist, dealing with blood and body fluids, McCullough said the vaccine is appropriate for him, but babies are not at risk for it unless their mother has the illness or is an active IV drug user. For most babies, he said, it is a “completely unnecessary shot on the first day of life.”

The Centers for Disease Control and Prevention (CDC) in October 2023 recommended newborns receive Beyfortus, the monoclonal antibody shot meant to protect babies from RSV-related illness.

“This has no safety track record,” he said. “We’ve never given a synthetic antibody to a baby ever in the history of medicine, and now it’s being given uniformly with no idea of what is going to happen to the baby’s immune system over the next several weeks or months.”

The clinical trials were inconclusive as to whether Beyfortus is safe, and evidence from France shows increased mortality among infants after the shot was introduced, he said.

McCullough said the broader safety concerns stem largely from the fact that so many are given in combination. “For some babies, it’s too much,” he said.

Excessive vaccination, he explained, sends the immune system into overdrive, which can lead a baby to develop a fever and a febrile seizure (convulsion).

Research shows febrile seizures have about a 40% chance of causing permanent neurologic injury, ranging from epilepsy to attention-deficit/hyperactivity disorder to autism spectrum disorder.

Staver said many parents who saw their children develop autism post-vaccination are told either that it isn’t true or it’s just a coincidence because there is no evidence of such a link.

“The direct observation by a mother and father of their child is the strongest evidence,” McCullough said, citing Dr. Andy Wakefield’s controversial 1998 study.

McCullough also cited a recent study by the Children’s Health Defense science team, which showed that combining multiple vaccines is dangerous. Spacing them out and giving them individually — rather than combining three vaccines into one shot, like the measles-mumps-rubella, or MMR, vaccine — is safer, he said.

And, he said, all children do not need all vaccines. Which vaccines a child gets should be determined on a risk basis. For example, a child with cystic fibrosis might need the respiratory illness vaccines, but healthy kids probably don’t.

Yet these vaccines are given to all children in part, he said, because the people who advise the CDC on which vaccines should be recommended for children have serious conflicts of interest — most take money from Big Pharma. Then schools enact mandates based on those recommendations, leaving parents feeling as if they have no choice.

Vaccine makers lobby state legislators to continually increase the list of mandatory vaccines.

McCullough said:

“Can you imagine if you had a product that treats an illness? You would have to treat a small number of people in a population. But if you have a vaccine, that means the whole entire population has to receive the product.

“A product that must be purchased by the entire population with no liability is an absolute boon to any purveyor of that product.”

McCullough said the CDC has turned a blind eye to vaccine safety. For example, none of the childhood vaccines have been studied for safety when given in combination.

He added that Dr. Paul Thomas reported in The Defender that pediatricians receive substantial incentives from insurance companies to vaccinate certain high percentages of their patients.

For lower-income kids, there is also government financial support to ensure that the vast majority of the population is vaccinated against legacy diseases like diphtheria, tetanus, polio and other diseases that are either no longer commonly circulating or for which good treatments exist.

For many, McCullough said, the recommendation that children take the COVID-19 vaccine, given its alarming safety data, was “the last straw.”

“That act was irresponsible. It triggered the World Council for Health, which is an evidence-based, consensus-driven body to recommend waiting on all the childhood vaccines,” he said.

Vaccines are not safe or effective enough to mandate, McCullough said. “Every parent and child unit should be able to make their own decisions free of any pressure, coercion, or threat of reprisal.”

Watch the interview here.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 20, 2024 Posted by | Science and Pseudo-Science | , , | Leave a comment

COVID-19 Vaccines Cause far More Myocarditis than Infection, Overall Risks Greatly Outweigh Theoretical Benefits

BREAKING PUBLICATION

By Peter A. McCullough, MD, MPH | Courageous Discourse™ | August 19, 2024

When the Springer Nature CUREUS Journal of Biomedical Sciences retracted one of the most comprehensive and valid risk-benefit analyses of the COVID-19 vaccines, they probably had no idea the message would be greatly amplified and now fully published in a pair of papers in the International Journal of Vaccine Theory, Practice, and Research.

This manuscript evaluated all of the published data and has completely overturned a false narrative held by government agencies and the American College of Cardiology who erroneously assert that SARS-CoV-2 infection poses a greater risk of heart damage than vaccination. Mead et al importantly conclude the vaccines cause actual adjudicated and oftentimes fatal myocarditis while the infection remains a theoretical risk without adjudicated, autopsy proven cases.

COVID-19 Modified mRNA “Vaccines”: Lessons Learned from Clinical Trials, Mass Vaccination, and the Bio-Pharmaceutical Complex, Part 2. (2024). International Journal of Vaccine Theory, Practice, and Research 3(2), 1246-1315. https://doi.org/10.56098/w66wjg87

The paper goes into great depth to enumerate harms from the shot along the lines of six domains where observed adverse events greatly outweigh claimed, theoretical benefits:

“We then categorize the principal adverse events associated with the modmRNA products with a brief systems-based synopsis of each of the six domains of potential harms: (1) cardiovascular, (2) neurological, (3) hematologic; (4) immunological, (5) oncological, and (6) reproductive. We conclude with a discussion of the primary public health and regulatory issues arising from this evidence-informed synthesis of the literature and reiterate the urgency of imposing a global moratorium on the modmRNA-LNP-based platform.”

The final call is clear, the COVID-19 mass, indiscriminate vaccination campaign should come to an end and with it, the four-year long false “safe and effective” narrative from the Bio-Pharmaceutical Complex.

August 19, 2024 Posted by | Science and Pseudo-Science | | Leave a comment

Calley & Casey Means: The Truth About Ozempic, the Pill, and How Big Pharma Keeps You Sick

TCN | August 17, 2024

August 18, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | | Leave a comment

What’s Really Happening with Mpox

The Mpox Emergency

By David Bell | Brownstone Institute | August 18, 2024

The World Health Organization (WHO) acted as expected this week and declared Mpox a Public Health Emergency of International Concern (PHEIC). So, a problem in a small number of African countries that has killed about the same number of people this year as die every four hours from tuberculosis has come to dominate international headlines. This is raising a lot of angst from some circles against the WHO.

While angst is warranted, it is mostly misdirected. The WHO and the IHR emergency committee they convened had little real power – they are simply following a script written by their sponsors. The African CDC, which declared an emergency a day earlier, is in a similar position. Mpox is a real disease and needs local and proportionate solutions. But the problem it is highlighting is much bigger than Mpox or the WHO, and understanding this is essential if we are to fix it.

Mpox, previously called Monkeypox, is caused by a virus thought to normally infect African rodents such as rats and squirrels. It fairly frequently passes to, and between, humans. In humans, its effects range from very mild illness to fever and muscle pains to severe illness with its characteristic skin rash, and sometimes death. Different variants, called ‘clades,’ produce slightly different symptoms. It is passed by close body contact including sexual activity, and the WHO declared a PHEIC two years ago for a clade that was mostly passed by men having sex with men.

The current outbreaks involve sexual transmission but also other close contact such as within households, expanding its potential for harm. Children are affected and suffer the most severe outcomes, perhaps due to issues of lower prior immunity and the effects of malnutrition and other illnesses.

Reality in DRC

The current PHEIC was mainly precipitated by the ongoing outbreak in the Democratic Republic of Congo (DRC), though there are known outbreaks in nearby countries covering a number of clades. About 500 people have died from Mpox in DRC this year, over 80% of them under 15 years of age. In that same period, about 40,000 people in DRC, mostly children under 5 years, died from malaria. The malaria deaths were mainly due to lack of access to very basic commodities like diagnostic tests, antimalarial drugs, and insecticidal bed nets, as malaria control is chronically underfunded globally. Malaria is nearly always preventable or treatable if sufficiently resourced.

During this same period in which 500 people died from Mpox in DRC, hundreds of thousands also died in DRC and surrounding African countries from tuberculosis, HIV/AIDS, and the impacts of malnutrition and unsafe water. Tuberculosis alone kills about 1.3 million people globally each year, which is a rate about 1,500 times higher than Mpox in 2024.

The population of DRC is also facing increasing instability characterized by mass rape and massacres, in part due to a scramble by warlords to service the appetite of richer countries for the components of batteries. These in turn are needed to support the Green Agenda of Europe and North America. This is the context in which the people of DRC and nearby populations, which obviously should be the primary decision-makers regarding the Mpox outbreak, currently live.

An Industry Produces What It Is Paid for

For the WHO and the international public health industry, Mpox presents a very different picture. They now work for a pandemic industrial complex, built by private and political interests on the ashes of international public health. Forty years ago, Mpox would have been viewed in context, proportional to the diseases that are shortening overall life expectancy and the poverty and civil disorder that allows them to continue. The media would barely have mentioned the disease, as they were basing much of their coverage on impact and attempting to offer independent analysis.

Now the public health industry is dependent on emergencies. They have spent the past 20 years building agencies such as CEPI, inaugurated at the 2017 World Economic Forum meeting and solely focused on developing vaccines for pandemic, and on expanding capacity to detect and distinguish ever more viruses and variants. This is supported by the recently passed amendments to the International Health Regulations (IHR).

While improving nutrition, sanitation, and living conditions provided the path to longer lifespans in Western countries, such measures sit poorly with a colonial approach to world affairs in which the wealth and dominance of some countries are seen as being dependent on the continued poverty of others. This requires a paradigm in which decision-making is in the hands of distant bureaucratic and corporate masters. Public health has an unfortunate history of supporting this, with restriction of local decision-making and the pushing of commodities as key interventions.

Thus, we now have thousands of public health functionaries, from the WHO to research institutes to non-government organizations, commercial companies, and private foundations, primarily dedicated to finding targets for Pharma, purloining public funding, and then developing and selling the cure. The entire newly minted pandemic agenda, demonstrated successfully through the Covid-19 response, is based on this approach. Justification for the salaries involved requires detection of outbreaks, an exaggeration of their likely impact, and the institution of a commodity-heavy and usually vaccine-based response.

The sponsors of this entire process – countries with large Pharma industries, Pharma investors, and Pharma companies themselves – have established power through media and political sponsorship to ensure the approach works. Evidence of the intent of the model and the harms it is wreaking can be effectively hidden from public view by a subservient media and publishing industry. But in DRC, people who have long suffered the exploitation of war and the mineral extractors, who replaced a particularly brutal colonial regime, must now also deal with the wealth extractors of Pharma.

Dealing with the Cause

While Mpox is concentrated in Africa, the effects of corrupted public health are global. Bird flu will likely follow the same course as Mpox in the near future. The army of researchers paid to find more outbreaks will do so. While the risk from pandemics is not significantly different than decades ago, there is an industry dependent on making you think otherwise.

As the Covid-19 playbook showed, this is about money and power on a scale only matched by similar fascist regimes of the past. Current efforts across Western countries to denigrate the concept of free speech, to criminalize dissent, and to institute health passports to control movement are not new and are in no way disconnected from the inevitability of the WHO declaring the Mpox PHEIC. We are not in the world we knew twenty years ago.

Poverty and the external forces that benefit from war, and the diseases these enable, will continue to hammer the people of DRC. If a mass vaccination campaign is instituted, which is highly likely, financial and human resources will be diverted from far greater threats. This is why decision-making must now be centralized far from the communities affected. Local priorities will never match those that expansion of the pandemic industry depends on.

In the West, we must move on from blaming the WHO and address the reality unfolding around us. Censorship is being promoted by journalists, courts are serving political agendas, and the very concept of nationhood, on which democracy depends, is being demonized. A fascist agenda is openly promoted by corporate clubs such as the World Economic Forum and echoed by the international institutions set up after the Second World War specifically to oppose it. If we cannot see this and if we do not refuse to participate, then we will have only ourselves to blame. We are voting for these governments and accepting obvious fraud, and we can choose not to do so.

For the people of DRC, children will continue to tragically die from Mpox, from malaria, and from all the diseases that ensure return on investment for distant companies making pharmaceuticals and batteries. They can ignore the pleading of the servants of the White Men of Davos who will wish to inject them, but they cannot ignore their poverty or the disinterest in their opinions. As with Covid-19, they will now become poorer because Google, the Guardian, and the WHO were bought a long time back, and now serve others.

The one real hope is that we ignore lies and empty pronouncements, refusing to bow to unfounded fear. In public health and in society, censorship protects falsehoods and dictates reflect greed for power. Once we refuse to accept either, we can begin to address the problems at the WHO and the inequity it is promoting. Until that time, we will live in this increasingly vicious circus.

David Bell, Senior Scholar at Brownstone Institute, is a public health physician and biotech consultant in global health. He is a former medical officer and scientist at the World Health Organization (WHO), Programme Head for malaria and febrile diseases at the Foundation for Innovative New Diagnostics (FIND) in Geneva, Switzerland, and Director of Global Health Technologies at Intellectual Ventures Global Good Fund in Bellevue, WA, USA.

August 18, 2024 Posted by | Corruption, Deception, Mainstream Media, Warmongering, Science and Pseudo-Science | , , | Leave a comment

Dear Elon, 1,000ppm of carbon dioxide is safe, we breathe it every day

Elon is scratching for a reason to keep worrying about CO2

By Jo Nova | August 16, 2024

In the interview with Donald Trump, Elon Musk tried to argue that we ought be limiting carbon dioxide because we are too close to 1,000ppm where people get headaches. Not to put too fine a point on it, but we breath out air at 40,000 ppm fifteen times a minute for our entire lives. If 1,000 ppm gave us a headache or made us nauseous, we’d have to hold our breath every time we kissed someone.

@ElonMusk:  The point I was making is that, even if CO2 did not cause global warming, it is uncomfortable to breathe air with >1000 ppm of CO2. Given that the outdoor ppm away from cities is now ~420 (lol), it is already getting close to 1000 ppm indoors in cities at times. You can buy a cheap CO2 monitor and measure this for yourself.

As the global base level of CO2 keeps increasing, it will cause air quality in cities to feel stuffy and unpleasant, resulting in drowsiness, poor concentration and eventually headaches and nausea. That would not be a good future.

And then he quotes CO2meter.com which, ahem, sells CO2 meters, and has an incentive to wildly overstate the problems with CO2, which they do.

CO2 is not the problem, the stale air and other pollutants cause headaches and sleepiness.

The point of CO2 meters is not so much to warn us about excessive CO2 levels, but to indicate how well the room is ventilated.  CO2 levels are just an indicator for air quality. Air with higher CO2 levels usually also has higher levels of organic compounds, humidity, body odour, mold, chemicals from furniture and paint (like formaldehyde) and potentially viruses too. When people report headaches and nausea, the high CO2 levels are not the issue, it’s the bioeffluence that causes problems. When researchers do cognitive tests with pure CO2 added to clean air, performances don’t suffer.  The stale air is the problem, not the CO2. (See Zhang, and Misra where they compared the cognitive effects from badly ventilated air and clean air with high CO2 levels up to 3,000ppm. Problems disappear when they use fresh air plus higher CO2.) Well ventilated rooms may also be cooler rooms, which might explain why results so often contradict each other.

Classrooms are at 1,000ppm “typically”

While outdoor air is 420ppm, indoor levels of CO2 are commonly 1,000ppm in classrooms every day, and can rise as high as 3,000ppm if all the windows are shut. The recognized occupational health and safety levels for long term working exposure are 5,000 ppm for 8 hours straight, five days a week. It’s no big deal.

The National Collaborative Centre for Environmental Health (Canada) measured school and buildings and advises that “Typically, in an occupied classroom situation, the recommended level of ventilation would correspond to a CO2 level of approximately 1000-1100 ppm“. Furthermore, they said the “lowest level at which a human health effect (i.e. acidosis) has been observed in humans is 7,000 ppm, and that only after several weeks of continuous exposure in a submarine environment”.

The occupational limits for CO2recommended by the American Conference of Governmental Industrial Hygienists (ACGIH) are 5000 ppm (TLV-TWA) and 30,000 ppm (TLV-STEL), based on the direct effects on acidification of the blood.  — via Marc Morano and Climate Depot

 Station views of Russian Modules during VKD-51 spacewalk

At NASA The Office of the Chief Health and Medicial Officer reports that a typical spacecraft works at around 3,000-7,000 ppm (or o.3-0.7% CO2). The recommended exposure is 5,000, and the permissible exposure limit is 10,000 ppm. Although the flight surgeons found levels of nearly 7,000 were safe and “didn’t affect performance”. On Apollo 13, CO2 levels rose to 20,000ppm. Sweating and shortness of breath became a problem above 30,000 ppm.

Submariners typically live with CO2 levels of 2,000- 5,000 ppm, and when a small sample of sailors was tested at 600, 2500 or 15,000 ppm, the researchers couldn’t find any difference in results from an 80 minute test on decision making. (Rodeheffer at al) Likewise another study at the Johnson Space Centre, people did cognition tests at 600, 1,200, 2,500 and 5,000ppm and there was no dose response effect. Results look rather random.

Lowther et al looked at 51 studies in 2021, and found nothing conclusive in terms of harms from CO2 below 5,000ppm. Most studies were confounded, results were conflicting. Teams of researchers are hunting to find another problem “due to CO2”. If there was a strong negative effect of CO2 it would have shown up by now. Instead CO2 is only associated with occasional headaches and nausea — probably because it is high in crowded rooms with little ventilation.

One large review in 2019 was described as showing CO2 affected people at levels as low as 1,000ppm, but the paper itself  points at the confounding data and uses the words “possible” and “potential effects” and concludes “we need more studies.”

UPDATE: Commenters Alan Klein and Mr Farnham points out the safety limits for Australian coal miners (NSW) is 1.25% CO2 which is 12,500ppm, and that is for 8 hour shifts. Brief excursions up to 3% (30,000ppm) are acceptable. See comment #17 for more details.

REFERENCES

Lowther, Scott D., Sani Dimitroulopoulou, Kerry Foxall, Clive Shrubsole, Emily Cheek, Britta Gadeberg, and Ovnair Sepai. 2021. “Low Level Carbon Dioxide Indoors—A Pollution Indicator or a Pollutant? A Health-Based Perspective” Environments 8, no. 11: 125. https://doi.org/10.3390/environments8110125

Mishra AK, Schiavon S, Wargocki P, Tham KW. Respiratory performance of humans exposed to moderate levels of carbon dioxide. Indoor Air. 2021 Sep;31(5):1540-1552. doi: 10.1111/ina.12823. Epub 2021 May 15. PMID: 33991134.

Rodeheffer CD, Chabal S, Clarke JM, Fothergill DM. Acute Exposure to Low-to-Moderate Carbon Dioxide Levels and Submariner Decision Making. Aerosp

Zhang X, Wargocki P, Lian Z, Thyregod C. Effects of exposure to carbon dioxide and bioeffluents on perceived air quality, self-assessed acute health symptoms, and cognitive performance. Indoor Air. 2017 Jan;27(1):47-64. doi: 10.1111/ina.12284. Epub 2016 Mar 7. PMID: 26825447.

h/t to Willie Soon, Marc Morano and Climate Depot.

August 18, 2024 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular | Leave a comment