Aletho News

ΑΛΗΘΩΣ

‘Monster’ Fauci should be jailed – Joe Rogan

RT | January 10, 2025

Hollywood star Mel Gibson and presenter Joe Rogan have claimed that former chief medical adviser Anthony Fauci should face prosecution, as they discussed his influence on the American healthcare system over the years. The popular American podcast host labelled the ex-government official a “monster.”

Fauci became the public face of the federal government’s response to the Covid-19 pandemic both under President Donald Trump and President Joe Biden. The imposition of restrictive measures and the scientist’s reported involvement in suppressing the theory that the virus may have originated from US-funded gain-of-function research in China have made Fauci a controversial figure.

Gibson was a guest on the Joe Rogan Experience podcast on Thursday. Both men wondered how Fauci was “still walking around,” or “at least free” after his actions during the pandemic.

They were discussing the 2021 book by Robert F. Kennedy Jr. titled ‘The Real Anthony Fauci’. The author, a healthcare campaigner turned politician, described Fauci as an official in cahoots with big pharmaceutical corporations, who had abused his power for decades. The HIV/AIDS epidemic in the US was one of the main topics of the book.

”That book is an accurate depiction of what Anthony Fauci did during the AIDS crisis, which probably was an AZT crisis,” Rogan claimed.

He was referring to the antiretroviral medication azidothymidine. It was the first to be used en masse in the late 1980s to suppress HIV and had serious side effects. Kennedy claimed that Fauci, in his role as the director of the National Institute of Allergy and Infectious Diseases (NIAID), improperly endorsed AZT and downplayed its side effects while undermining possible alternative treatments.

”I drove up to San Francisco and I listened to it and I had road rage,” Gibson said, recalling his reaction to the book.

”If this is true, what the f**k is going on and how is that monster still loose?” Rogan asked. Meanwhile, the outgoing Biden administration is considering “giving him a full pardon – it’s like f**king crazy.”

Fauci’s name came up as the two were criticizing mainstream media for its “complicity” in protecting for-profit healthcare in the US. Gibson recalled how Rogan was attacked by news outlets for taking the drug ivermectin after testing positive for Covid-19 in 2021.

The medicine is widely used to treat parasites in humans in Africa. But the media dismissed it as a “horse dewormer” – the drug’s usual application in the US – as they urged the public to vaccinate against Covid-19.

January 11, 2025 Posted by | Mainstream Media, Warmongering, War Crimes | , , , , , | Leave a comment

Facebook Dumps ‘Fact-checkers’ One Day After CHD Asks Supreme Court to Hear Censorship Case Against Meta

By Suzanne Burdick, Ph.D. | The Defender | January 7, 2025

Less than 24 hours after Children’s Health Defense (CHD) petitioned the U.S. Supreme Court to hear its censorship case against Facebook’s parent company, Meta, Mark Zuckerberg announced the company is ending its third-party “fact-checking” program.

“It’s time to get back to our roots around free expression on Facebook and Instagram,” Zuckerberg told viewers in a press release video. Meta also owns Instagram.

CHD sued Meta in November 2020 over the social media giant’s censorship practices. The company de-platformed CHD from Facebook and Instagram in August 2022 and has not reinstated the accounts.

Commenting on today’s news, CHD CEO Mary Holland told The Defender, “It’s clear that Mark Zuckerberg is worried about new anti-censorship policies of the incoming administration — as he should be. The record in CHD v. Meta clearly shows Facebook’s close collaboration with the White House to censor vaccine-related speech, even pre-COVID.”

Holland added:

“CHD has taken its case to the Supreme Court, and Facebook doubtless realizes there are Justices there that are very dubious about Facebook’s role in censoring speech at the behest of the government in the new public square.

“Zuckerberg may imagine that by making this announcement he is mooting this case, or making it no longer significant. That’s not the situation — the country needs closure that this kind of fusion of state and industry to censor unwanted information will never happen again.”

CHD’s lawsuit against Facebook’s parent company, Meta, and its founder and CEO, Zuckerberg, alleges that government actors partnered with Facebook to censor the plaintiffs’ speech — particularly speech related to vaccines and COVID-19 — that should have been protected under the First Amendment.

The suit also named “fact-checking” firms Science Feedback, and the Poynter Institute and its PolitiFact website. On Aug. 9, 2024, the 9th Circuit U.S. Court of Appeals ruled against CHD.

Lawyers with CHD urged the Supreme Court to reconsider the decision. They wrote in their petition, filed Monday:

“This case goes to the heart of our constitutional design, raising critical questions in the Internet Age about the availability of open debate free from government censorship-by-proxy.

“The practical consequences of leaving the decision below intact are enormous: the levers of censorship on the mega-platforms will always be sore temptation for executive office-holders — and not just about vaccines or Covid.”

National healthcare and constitutional practice attorney Rick Jaffe called Meta’s announcement a “very big deal for the country and for CHD.”

Jaffe represents CHD in some of its cases, including cases involving doctors’ right to speak freely about COVID-19. He told The Defender :

“For the last five-plus years, CHD — largely through Robert F. Kennedy Jr., Mary Holland, and the group’s supporters — have been at the forefront of defending free speech on social media … Meta’s action today shows the effect of the changing public’s view on censorship by social media companies which Meta could no longer ignore.

“So, congrats to CHD and its legal team who helped this happen. The work isn’t over yet, so onwards.”

Meta shifts to content moderation model used on X

Rather than turning to third parties to fact-check posts, Meta will use a “Community Notes model” in which social users themselves decide when posts are potentially misleading and need more context, said Meta’s Chief Global Affairs Officer Joel Kaplan in a statement. “We’ve seen this approach work on X,” Kaplan said.

The change will take a few weeks to implement, Kaplan said.

Meta also will lift restrictions on topics such as immigration and gender identity. “It’s not right that things can be said on TV or the floor of Congress, but not on our platforms,” Kaplan said.

The Defender asked Meta if it will lift restrictions on discussions about vaccine safety and COVID-19 but did not receive a response by deadline.

Meta is also changing how it enforces its policies. “Up until now,” Kaplan said, “we have been using automated systems to scan for all policy violations, but this has resulted in too many mistakes and too much content being censored that should haven’t been.”

Zuckerberg said there’s “legitimately bad stuff out there — drugs, terrorism, child exploitation.” The company will continue to take those things “very seriously” by using automated systems to scan for them.

However, for less severe violations, Meta will rely on a person reporting an issue before taking action against an account user.

Zuckerberg said he always cared about freedom of expression but that in recent years, his company responded to pressure for stricter speech restrictions. “Governments and legacy media have pushed to censor more and more,” Zuckerberg said. “A lot of this is clearly political.”

He acknowledged that some of the “complex systems” Meta built to moderate content made mistakes. “We’ve reached a point where it’s just too many mistakes and too much censorship.”

Will Meta’s policy changes stick?

Zuckerberg said Meta’s policy changes were also prompted by the recent U.S. elections that were a “cultural tipping point toward once again prioritizing free speech.”

Jenin Younes, a civil rights attorney who represented some of the plaintiffs in the landmark censorship case Murthy v. Missouri, told The Defender she was “cautiously optimistic” about Meta’s announcement.

Meta appeared to be making the changes because of a new presidential administration, Younes said. “That means that Meta could change course in another four years under a different administration. We need major social media platforms — the modern public square — to adopt principled free speech positions that don’t change with the wind.”

If platforms don’t adopt strong free speech positions, public dialogue suffers, Younes said. “Censorship on Meta, especially during the COVID era, strangled public debate and even went so far as to prevent vaccine-injured individuals from corresponding with each other in private groups.”

Kim Mack Rosenberg, CHD general counsel, told The Defender Meta’s announcement does not undo the years of the damage done to CHD and many other individuals and groups.

“What is important is not only that Meta is making these changes but also that steps are taken to make sure this cannot be repeated, which makes our ongoing cases — including the recently filed petition to the U.S. Supreme Court — critically important.”

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.

January 7, 2025 Posted by | Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science | , , , , | Leave a comment

FDA responds to study on DNA contamination in Pfizer vaccine

Maryanne Demasi, reports | January 6, 2025

The U.S. Food and Drug Administration (FDA) has responded to a peer-reviewed study conducted within its own laboratory, which uncovered excessively high levels of DNA contamination in Pfizer’s mRNA COVID-19 vaccine.

The study revealed that residual DNA levels exceeded regulatory limits by 6 to 470 times, validating earlier studies from independent researchers that the FDA had previously disregarded.

Published by students in the Journal of High School Science, the study has garnered significant attention since the story broke, with its altimetric score rivalling those of major studies in leading medical journals.

FDA’s Response

Despite the study being conducted at the FDA’s White Oak campus in Maryland, the agency has sought to distance itself from the findings.

A spokesperson stated that the study “does not belong to the FDA” and is therefore not theirs to disclose.

“The FDA does not comment on individual studies,” the spokesperson added, declining to acknowledge the new scientific findings.

The agency also refused to address the involvement of three of its own scientists—Dr Shuliang Liu, Dr Tony Wang, and Dr Prabhuanand Selvaraj—who supervised the students conducting the study.

When questioned about potential regulatory actions, such as issuing a public alert, recalling affected vaccine batches, or notifying other agencies, the FDA stood firm in its defence of mRNA vaccine safety.

“Based on a thorough assessment of the entire manufacturing process by the agency’s scientific experts, the FDA is confident in the quality, safety, and effectiveness of the COVID-19 vaccines that the agency has approved and authorised,” stated the FDA spokesperson.

“The agency’s benefit-risk assessments and ongoing safety surveillance demonstrate that the benefits of their use clearly outweigh their risks. Additionally, with over a billion doses of the mRNA vaccines administered, no safety concerns related to residual DNA have been identified.”

This statement effectively shuts down any immediate plans for further investigation.

Calls for Accountability

The FDA’s response has provoked sharp criticism from scientists. Genomics expert Kevin McKernan, who first identified excessive DNA contamination in Pfizer vials in early 2023, called the agency’s stance evasive and deeply concerning.

“It’s the same script on auto-repeat at every regulatory agency,” McKernan said.

“They always say, ‘billions of doses given, benefits outweigh the risks, we’ve seen no evidence of harm.’ But billions of cigarettes were smoked too, and that didn’t make them safe.”

McKernan also questioned the FDA’s attempts to distance itself from the study.

“If the FDA supplied the materials for the study and provided technical advice through staff supervision, then how can they not be responsible for the data?” McKernan asked. “Do they only deny their connection when the data becomes inconvenient?”

Professor Nikolai Petrovsky, Professor of Immunology and Infectious Disease at the Australian Respiratory and Sleep Medicine Institute, shared McKernan’s concerns.

“The FDA’s response is extremely disappointing,” he said.

“It completely circumvents whether or not the level of DNA contamination in mRNA vaccines exceeds regulatory limits (as the study performed in their lab would indicate), and what they intend to do about it.”

“Just claiming there’s no safety issue and pointing to the billions of doses administered, without offering any evidence of safety, is far from satisfactory,” added Prof Petrovsky.

Regulatory Silence

The Australian Therapeutic Goods Administration (TGA), which has previously dismissed similar findings from independent researchers as “misinformation,” was contacted for comment but did not provide a response before publication.

Russell Broadbent, Victorian Member for Monash, expressed his disbelief at the regulatory inaction.

“I cannot fathom why the TGA isn’t making this their number one priority, given their charter is to regulate therapeutics to help ensure Australians stay healthy and safe,” he said.

In light of the FDA laboratory findings, Broadbent urged regulators to “immediately pause the rollout of the vaccines, and investigate the claims.”

The Stakes Could Not Be Higher

These revelations carry immense implications. mRNA vaccines are hailed as the dawn of a new era in vaccinology, with the world increasingly relying on this platform technology to supersede traditional vaccine methods.

Failure to address the safety of this technology will torpedo public trust in both the vaccines and the regulatory systems meant to ensure their safety.

“The public deserves clear answers, not regulatory hand-waving,” McKernan said.

As calls for accountability grow louder, the FDA faces mounting pressure to engage with the scientific evidence—particularly that which originates from its own laboratory.


NB: a comprehensive critique of the student study from FDA’s lab has been published by Kevin McKernan.

January 6, 2025 Posted by | Science and Pseudo-Science | , , , | Leave a comment

The Risks of Vaccines During Pregnancy

What Expecting Mothers Need to Know

By Tracy Slepcevic | Warrior Mom | January 2, 2025

Pregnancy is a time of joy, anticipation, and careful decision-making. As an expecting mother, your primary goal is to ensure the health and safety of your baby. However, amidst the abundance of information and recommendations, it’s important to understand the potential risks associated with vaccines during pregnancy. Despite assurances from health authorities, recent evidence and expert testimonies suggest that vaccines given during pregnancy pose a significant risk to both mother and baby.

Lack of Proper Testing for Pregnant Women

One of the most concerning aspects of vaccine recommendations for pregnant women is the lack of rigorous safety testing. During a 2023 FDA meeting, Dr. Meryl Nass highlighted the troubling fact that many vaccines routinely recommended during pregnancy, including the COVID-19 vaccine, were not adequately tested in pregnant populations. The FDA admitted that its recommendations are based on limited or no data from controlled clinical trials involving pregnant women.

This absence of reliable data leaves many unanswered questions about the long-term effects of vaccines on both the developing fetus and the mother’s immune system. The decision to recommend vaccines without sufficient evidence undermines informed consent and raises serious ethical concerns.

Alarming Reports of Adverse Effects

Adverse events following vaccination during pregnancy are increasingly being reported. These include:

  • Miscarriages: Some studies and anecdotal reports have linked vaccines, particularly the COVID-19 vaccine, to an increase in pregnancy losses.
  • Preterm Births: Concerns have been raised about a potential connection between maternal vaccination and preterm deliveries.
  • Developmental Issues: Emerging evidence suggests the possibility of long-term developmental effects on the baby, though more research is urgently needed to confirm these findings.

Dr. James Thorp, a board-certified OB-GYN, has been vocal about the risks of vaccinating pregnant women, stating that the CDC’s recommendations lack robust scientific backing. Dr. Thorp and other experts argue that the precautionary principle should guide decisions regarding vaccines during pregnancy, especially when there are alternative ways to manage risks.

The Role of Adjuvants and Ingredients

Many vaccines contain adjuvants; these are substances added to enhance immune response. Aluminum-based adjuvants, for example, have raised concerns due to their neurotoxic effects. During pregnancy, the developing fetus is particularly vulnerable to toxins, and the accumulation of such substances may interfere with normal development.

The presence of viral DNA fragments and other contaminants in vaccines has also been flagged as a risk factor. These components are not fully studied in the context of pregnancy, further complicating the risk assessment.

Trusting Your Natural Immunity

God did not make a mistake, man did. Pregnancy is a time when the body’s immune system undergoes natural adjustments to protect both the mother and the baby. Our God-given immunity is remarkably capable of managing many potential threats without external interventions. Prioritizing a healthy diet, reducing stress, and ensuring adequate sleep can support your immune system during this critical time.

Steps to Protect Yourself and Your Baby

If you are pregnant or planning to become pregnant, here are some steps you can take to make informed decisions about vaccines:

  1. Ask Questions: Before agreeing to any vaccination, ask your healthcare provider about the evidence supporting its safety and efficacy during pregnancy. Most doctors are blinded by the dangers of vaccines or choose to keep us in the dark due to kickbacks from Big Pharma.
  2. Do Your Research: Explore independent studies and expert testimonies to gain a fuller understanding of potential risks. The research is out there, but you will have to dig deeper than a Google search.
  3. Consider Alternatives: For certain infections, there may be natural or non-invasive ways to protect yourself without compromising your baby’s development. Boost your immune system with supplements instead of neurotoxic vaccines.
  4. Seek Second Opinions: If you feel pressured by your provider, consult with another healthcare professional to discuss your concerns. Functional and Alternative medicine doctors are more likely to keep their oath to “do no harm.”
  5. Prioritize Wellness: Focus on boosting your natural immunity through nutrition, hydration, and lifestyle choices.

A Call for Transparency and Caution

As an expecting mother, you deserve complete and honest information to make the best decisions for your baby. The current vaccine recommendations for pregnancy often lack the robust safety data needed to ensure their efficacy and safety. Until comprehensive studies are conducted and transparency is prioritized, the precautionary principle should guide decisions about vaccines during pregnancy.

By taking the time to educate yourself and trust your instincts, you can protect both your health and the health of your baby. Remember, it’s your right to make informed choices about your body and your baby’s future. For more information go to http://www.WarriorMom.com and http://www.AutismHealth.com.

January 5, 2025 Posted by | Science and Pseudo-Science, Timeless or most popular | , | Leave a comment

Karmageddon

Iyah May | December 18, 2024

While ‘Karmageddon’ has sparked significant conversation and controversy, Iyah has stood her ground. She refused to compromise her vision when asked to change a key lyric line, leading to the end of her contract with her manager. She chose to walk away from her record label and now, fully independent, Iyah continues to carve her own path as an artist.

Her fearless approach is shaped by her unique perspective as a qualified medical doctor, having worked on the frontlines during the COVID-19 pandemic.

LYRICS:
I open up my phone on a Monday morning
Staring at my screen
I’m tired and a little lonely
Mr Musk he said some shit the lefts are angry
Twitter wars and Gaza man it’s overwhelming
Maybe that’s how life becomes when
People less important than a profit line
No one cares about your dreams just pay
Your tax on time
Keep scrolling
Hold me near to you now
Gender, guns, religion and abortion rights
You better pick a tribe and hate the other side
Keep scrolling
But did you see Taylor live?

Man made virus watch the millions die
Biggest profit of their lives
Here’s inflation that’s your prize
This is Karmageddon
Turn on the news and eat their lies
Kim or Kanye pick a side
Cancel culture what a vibe
This is Karmageddon
Corporations swear they never lie
Politicians bribed for life
More than war it’s genocide
This is Karmageddon
Welcome to the chaos of the times
If you go left and I go right
Pray we make it out alive
This is Karmageddon

It’s fashion week celebs lose ribs
Balenciaga how’s the kids
Just ask Drake he’s losing beef
Kendrick killed him in his sleep
Diss tracks about beating up your queen
While women dying doesn’t cause a scene
While we’re fed all these distractions
Kids are killed from Israel’s actions
I’mma speak my mind
Sick to death of all these crazy lies
A circus for humanity’s decline
We just want a peaceful life give the people back their rights
And I’ve still got a beef
Cause Fauci’s laughing and we’ve been asleep
And WHO’s a liar and it’s running deep
Big pharma finna eat they a devil make them weak

Man made virus watch the millions die
Biggest profit of their lives
Here’s inflation that’s your prize
This is Karmageddon
Turn on the news and eat their lies
Kim or Kanye pick a side
Cancel culture what a vibe
This is Karmageddon
Corporations swear they never lie
Politicians bribed for life
More than war it’s genocide
This is Karmageddon
Welcome to the chaos of the times
If you go left and I go right
Pray we make it out alive
This is Karmageddon

Written by: Iyah May & Danny Duke
Performed by: Iyah May
Produced by: Danny Duke
Mixed by: Danny Duke
Mastered by: Chunkyluv
Video By: Brad Murnane
Edited By: Brad Murnane & Iyah May

January 1, 2025 Posted by | Ethnic Cleansing, Racism, Zionism, Video, War Crimes | , | Leave a comment

AARON SIRI TESTIFIES, NEW HAMPSHIRE: THE TRANSMISSION PARADOX

The HighWire with Del Bigtree | December 27, 2024

In the final installment of Siri Testifies: New Hampshire, ICAN’s lead attorney, Aaron Siri, presents a powerful testimony before the New Hampshire House Committee on COVID Response Efficacy. He tackles the critical question: do all vaccines stop transmission? With exclusive data and insights, this must-watch show challenges long-held assumptions and reshapes the public health conversation.

December 28, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | , | Leave a comment

Begging for the Wonder Drug

Five years later, we resolve never to forget how US hospitals deprived critically ill patients of ivermectin and other commonly used drugs that could have saved them.

Satoshi Ōmura, 2015 Nobel Laureate for his discovery of the ”wonder drug” Ivermectin, stands next to the River Blindness sculpture. His discovery cured this great scourge of the tropical world.
By John Leake | Courageous Discourse | December 13, 2024

As I was researching our book, The Courage to Face COVID-19: Preventing Hospitalization and Death While Battling the Bio-Pharmaceutical Complex, I was especially disturbed by countless stories of hospitals in various states who steadfastly refused to treat critically ill COVID-19 patients with ivermectin and other drugs (commonly used for other illnesses) that could have saved their lives.

I believe this episode constitutes the darkest chapter in the history of the U.S. hospital system. Strangely enough, the only serious legacy newspaper journalist in the entire country who covered it was Michael Capuzzo—formerly a reporter with the Miami Herald and the Philadelphia Inquirer, where he received four Pulitzer Prize nominations. Apart from Michael’s reporting . . . crickets.

Out of my conviction that we should never forget what U.S. hospitals did to patients who were consigned to die on ventilators instead of receiving FDA-approved, off-label drugs such as ivermectin, methylprednisolone, and even high dose aspirin, I am publishing our chapter on the extraordinary villains who committed this atrocity, and the good guys—including two great attorneys and humanitarians named Ralph Lorigo and Beth Parlato—who fought back. Please share this story with your friends and family and exhort them never to forget.


CHAPTER 28: Begging for the Wonder Drug

As Michael Capuzzo told the story in his long magazine piece “The Drug that Cracked Covid,” Judy Smentkiewicz was an eighty-year-old resident of Buffalo, New York. After working thirty-five years as an office manager for Metropolitan Life and raising two children, she had retired to her small house in the suburbs. A week after Senator Johnson’s second Senate hearing, she began preparing for Christmas, and looked forward to her two children, Michael and Michelle, visiting her for a few days. However, right after Michael and his wife arrived from Florida, she began to feel unwell. On December 22 she tested positive for Covid. Her kids were devastated and cancelled their Christmas celebration as Judy went into quarantine. A week later, she became short of breath and was rushed to the Millard Fillmore Suburban Hospital. On New Year’s Eve she was admitted to the ICU.

It was a terrible moment in which Judy and her children realized they might never see each other again. In the days that followed, the doctors and nurses with whom Michael spoke didn’t offer much hope. They said there were no medications for treating COVID-19 approved by federal health agencies apart from remdesivir. This was administered to Judy, but it seemed to have no beneficial effect. On New Year’s Eve, as her condition deteriorated, her two children and six of their friends gathered on the street below her hospital window and prayed for her.

Shortly after New Year’s Day, Michael received from his mother-in-law a video of Dr. Pierre Kory being interviewed by a reporter for Fox 10 News Now, KSAZ-TV in Phoenix, Arizona. That morning, Dr. Kory had given his Senate testimony on ivermectin. Michael watched it and was moved by Dr. Kory’s passionate intensity and eloquence. Immediately he called the hospital and told Judy’s attending physician that he wanted her to receive ivermectin. The doctor refused on the grounds that it wasn’t approved for COVID-19, but Michael refused to take no for an answer, and finally a hospital administrator approved one, 15-milligram dose. Less than twenty-four hours later, Judy was taken off the ventilator, and the next day she sat upright in a chair for a Zoom call with her son. She still wasn’t out of the woods, and when her heart started racing, she was moved to a cardiac unit, and the hospital refused to give her a second dose of ivermectin. Michael insisted but the hospital refused to budge.

And so, he contacted his friend and attorney Ralph Lorigo, and explained the situation. At the time, Lorigo knew nothing about ivermectin, so he too watched the interview with Dr. Kory, and then sued the hospital. New York State Supreme Court Judge Henry Nowak heard the case and ordered the hospital to commence treating Judy with four more doses of ivermectin, per her family doctor’s prescription.

The hospital refused to obey the judge’s order, which resulted in additional legal wrangling, including another hearing. Finally, the hospital’s lawyer agreed to allow Judy’s family doctor to administer the drug. He was under the impression it was on hand in the hospital’s pharmacy, but when he arrived to carry out his charge, he was told that it would have to be couriered from another facility. This caused another delay. Finally, at 11:00 pm that night, the second dose was administered, and she started to improve. Ten days later she walked out of the hospital.

As word spread about Judy’s happy outcome, Ralph Lorigo was contacted by countless others in the same situation, and soon his law firm had a new area of practice—trying to force hospitals to administer an FDA-approved, Nobel Prize winning, WHO “Essential Medication” to dying COVID-19 patients to whom nothing else was offered.

Mr. Lorigo was well-suited for the task. The energetic, punctilious attorney and Erie County Conservative party chairman has a formidable presence, with strong Italian good looks and a penchant for wearing beautifully tailored suit and power ties. Though he specialized in real estate law, he represented his clients seeking ivermectin with great care. A devoted family man with three children and multiple grandchildren, he empathized with the families who sought his help.

To be sure, it wasn’t an easy job, because the hospitals fought him tooth and nail, bringing multiple attorneys and expert witnesses to hearings. After a few more successes in which he prevailed and the patients recovered after receiving ivermectin, he received more queries than his staff could handle, so he contacted his friend, Beth Parlato, and asked her if she would be interested in taking some of the cases.

The 55-year-old attorney and mother of three had served as a judge in a New York State criminal court. Over the course of her career, she’d seen much of the good, the bad, and the ugly, but none of it had prepared her for the grueling path ahead. What she was about to witness would challenge all of her assumptions about the American healthcare and legal systems, and ultimately about human nature itself.

Most of her clients were referrals from the FLCCC, founded by Drs. Marik and Kory. The typical call would come into her office from a desperate husband or wife, daughter or son. Their stories were always the same. A much-loved family member had been languishing in hospital and was now headed for the ventilator and probable death. And though the doctors and nurses stated that the prognosis was poor, the hospital refused to administer ivermectin.

To patients and their families, the situation was incomprehensible. Many of Beth’s clients posed a variation of the question: “Mom [or dad] is declining and is probably going to die, so what’s the harm in her trying ivermectin?” Beth was at a loss for an answer. The hospital’s policy made no sense, neither as a matter of fact nor law. Many families wondered why “right to try” laws didn’t apply. Hospital attorneys claimed the “right to try” was only for experimental medications that were not yet FDA-approved. Ivermectin was FDA-approved, just not for the treatment of COVID-19.

Patients and their families found this argument perversely legalistic, but many judges—and all judges elected as Democrats—found it persuasive. Beth argued it was a legal, common, and longstanding medical practice to prescribe FDA-approved drugs off-label. Hospital attorneys retorted that the NIH guidelines for the treatment of COVID-19 did not recommend the off-label administration of ivermectin, and because the NIH was the final scientific arbiter of medical matters in the United States, the hospitals were required to follow its guidelines.

The trouble with the one-size-fits-all NIH guidelines for hospitalized COVID-19 patients was that they didn’t work. Almost a year into the pandemic, the United States had the highest COVID-19 death rate of the world’s top ten wealthiest nations and was in the top twenty nations with the highest death rates in the world. Approximately 80% of hospitalized patients who went on mechanical ventilation died. Also significant was the fact that that on January 14, 2021—in response to Senator Johnson’s letter requesting that the NIH review Dr. Kory’s presentation of evidence—the NIH dropped its recommendation against using ivermectin and adopted a neutral stance. Though far from satisfying for Dr. Kory and his colleagues, the NIH neutral stance at least gave doctors greater leeway to exercise their clinical judgement about the drug.

To make matters even more confusing, healthcare professionals were provided with broad legal immunity by the federal PREP Act (Public Readiness and Emergency Preparedness) of 2005. This authorized the Secretary of Health and Human Services to deploy a wide array of “Emergency Countermeasures” in the event of an infectious disease outbreak. When invoked by the Secretary of Health and Human Services, the PREP Act provides immunity for the “manufacture, testing, development, distribution, administration, and use of covered countermeasures.” On February 4, 2020, HHS Secretary Alex Azar declared COVID-19 an emergency and invoked the PREP Act.

The CARES Act of March 27, 2020, also provided immunity for healthcare workers treating COVID-19 patients. Additional immunity was granted by governors’ executive orders in all fifty states. The governor of New York State, in which Beth was practicing, provided the following immunity:

Conduct Covered: Civil liability for injury or death alleged to have been sustained directly as a result of an act or omission by person(s) covered.

Person(s) Covered: Physicians, physician assistants; specialist assistants; nurse practitioners; licensed registered professional nurses; licensed practical nurses.

Conduct Not Covered: Gross negligence.

Many observers who were documenting U.S. healthcare policy with respect to remdesivir wondered if all this liability protection could explain why the new, experimental drug was the hospital standard of care despite numerous red flags raised about its safety. The contrast of this policy with the strict policy against administering ivermectin was stunning.

Additionally, all the patients that Beth represented, and their families, stated in writing that they would indemnify the hospitals of liability for any adverse effects apparently caused by ivermectin, and that their primary care physicians would come to the hospital to administer it. Despite these multiple provisions of immunity, hospitals were still dead set against giving ivermectin to dying patients.

The hearings were brutal affairs in which hospital attorneys and expert witnesses portrayed Beth’s expert witness (on the safety and efficacy of ivermectin) as a delusional quack. Their most common line of attack was that Beth’s witness was a lone, eccentric voice in challenging the overwhelming scientific consensus that informed NIH guidelines. This rhetorical strategy ignored that many of mankind’s greatest scientific insights were the work of individuals who challenged the orthodoxy of their day. The growing body of evidence, including RCTs, cited by Beth’s witness was dismissed by hospital experts with the assertion that the evidence was “low quality.” Thus, the judge was presented with opposing expert witness claims about the evidence, only with the hospital’s witness also claiming he had “scientific consensus” and therefore the NIH on his side.

Beth tried to argue that the patient retained sufficient bodily autonomy to decide if he or she wished to take an FDA-approved drug off-label. The hospitals’ attorneys retorted that hospital patients had never had the right to decide their treatment, and that granting it with ivermectin would set a terrible precedent, opening a Pandora’s Box of future patients demanding treatments after hearing anecdotes about their efficacy. Beth regarded this argument as another legalistic dodge. Her clients weren’t presuming to practice medicine—they were dying men and women, desperately begging for the right to try an FDA-approved drug as a last and only hope when nothing else apart from remdesivir was being offered.

The hospitals claimed total sovereignty over the patient—a godlike power over all decisions affecting his life and death, with the patient afforded no say. For most gravely ill patients, the decision of this godlike power resulted in death. Thus, to sick patients and their families, the Lords of Healthcare were neither competent nor compassionate.

From: The Courage to Face COVID-19: Preventing Hospitalization and Death While Battling the Bio-Pharmaceutical Complex, by John Leake and Peter A. McCullough, MD, MPH, Foreword by Robert F. Kennedy Jr., Skyhorse, 2022.


POSTSCRIPT: As Dr. Pierre Kory noted in his book The War on Ivermectin, of the 80 lawsuits filed by lawyer Ralph Lorigo, in 40 the judge sided with the family, and in 40 with the hospital. Of those, in the 40 where patients received ivermectin, 38 survived, whereas of the 40 who did not, only 2 survived.

December 26, 2024 Posted by | Book Review, Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science, Timeless or most popular | , , , | Leave a comment

US shuts down ‘disinformation’ agency

RT | December 25, 2024

The US State Department’s Global Engagement Center (GEC) has shut down after Republicans cut its funding. The agency was responsible for spreading propaganda abroad and, according to conservatives, censoring dissident thought at home.

The GEC announced on Monday that it would cease operations by the end of that day. “The State Department has consulted with Congress regarding next steps,” the statement added.

The organization employed around 120 people and had an annual budget of $61 million. Established in 2016, its stated goal was to “recognize, understand, expose, and counter foreign state and non-state propaganda and disinformation efforts.”

In practice, the GEC spearheaded complex propaganda campaigns of its own. In two campaigns, the agency funded video games aimed at teaching children about the supposed dangers of anti-American narratives, releasing them in the UK, Ukraine, Latvia, Iraq, and Saudi Arabia.

During the coronavirus pandemic, the GEC funneled money to a range of NGOs which then compiled lists of social media accounts supposedly spreading “disinformation” about the virus and its origins, which were then presented to the platforms to be banned or removed. Many of the accounts belonged to what Twitter’s former trust and safety chief, Yoel Roth, called “ordinary Americans,” raising concerns among conservatives that the GEC was violating its prohibition on operating within the US.

In 2023, the GEC was forced to cut ties with George Soros’ ‘Global Disinformation Initiative’, after it emerged that the agency was paying Soros’ organization to compile lists of “high risk” news outlets to use in an advertiser boycott campaign. These news sites were predominantly right-leaning and American-based.

X owner Elon Musk called the GEC a “threat to our democracy” last year, describing the agency as the “worst offender in US government censorship [and] media manipulation.”

Musk was instrumental in finally shutting down the GEC. A mammoth 1,547-page spending bill put before the House of Representatives by Speaker Mike Johnson last week would have preserved funding for the agency, until Musk threatened to fund primary election challenges to any Republican who voted for it.

Musk decried the bill – which also included pay raises for lawmakers – as “criminal,” “outrageous,” “unconscionable,” and ultimately “one of the worst bills ever written.” President-elect Donald Trump and Vice President-elect J.D. Vance then released a joint statement against the bill, forcing Johnson to replace it with a trimmed-down piece of legislation totaling less than 120 pages.

This Musk-approved bill failed in a 235-174 vote, with 38 Republicans joining 197 Democrats to block its passage. It eventually passed after Republicans added a section suspending the US debt ceiling for two years, a move that will add trillions more to the federal government’s $36 trillion debt.

December 25, 2024 Posted by | Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science | , , , | Leave a comment

Covid-19 Vaccines White Clots Results – 2024

Medical Embalmers Across The Country

Dr. John Campbell | December 21, 2024

Rumble

Former Air Force Major Thomas Haviland surveyed embalmers in 2024 about unusual clots being found in the bodies of vaccinated deceased.

NEW YORK – I’ve seen the clots vary from case to case, since the covid shot came around, we have had many young deaths i.e.: 50-60 year-olds with massive heart attacks and every one of them has had clots as discussed in this survey, seems many people just want to turn a blind eye to it all, it’s a shame. As someone who’s been around this for about 12 years, I have never seen anything like this.

VIRGINIA – I’m finding a lot of the white rubbery clots and had been taking pictures of them but it’s become the new normal… I don’t use a drain tube anymore because of all the clots. blood clots and the fibrous white ones. My angular forceps is my to go instrument to help remove them…

OHIO – The past few years I have seen a significantly larger percentage of clotting in almost all embalmings. These white fibrous clots are definitely unusual having never seen them before 2021. Although not seeing the white fibrous clots or micro clotting in a larger percentage of deceased, the number of grape jelly clots has significantly increased from years past in all decedents.

IDAHO – Sometimes I am given the information about if someone has had a certain vaccine. Sometimes I am aware they have had 5-6 doses of it. These are the people we are seeing with the abnormal clots or significant amount of clots.

FLORIDA – With many embalmings that I have seen these clots in, I have had to inject in multiple points. Both with case’s refrigerated and prep done within a couple of hours after death.

FLORIDA – Seems like traditional “chicken fat clots” are less frequent being replaced with Jelly, Fibrous, Micro-clotting.

IOWA – Very thick and large, I have had some the whole diameter of the arteries and longer than a foot long.

LOUISIANA – Some of these fibrous blots come out as a whole, if done carefully, that mimic the arterial system. These clots are clearly the cause of demise of these decedents, but were legally labeled as heart issues, which are not typically autopsied to fully determine actual cause of death.

NORTH DAKOTA – I have had SEVERAL cases in 2020-2023 of the white fibrous clots and most had COVID listed as a factor on their death certificates. However, in each case the family did not know if the decedent was vaccinated.

FLORIDA – Unusual clots has changed since COVID vaccine I only took 2 vaccine Pfizer refuse to take booster nor vaccine again.

Exclusive: 70% of Embalmers Report Finding Strange Blood Clots Beginning in Mid-2021
https://childrenshealthdefense.org/defender/blood-clots-embalmers-report-mid-2021-covid-vaccines

Covid Vaccine Injury Global Study: http://www.react19.org/study

Covid vaccine injury medical expense fund: http://www.react19.org/donate

Original: https://youtu.be/sVpFs2VTgf8

=

https://www.youtube.com/@Campbellteaching

LinkedIn: https://www.linkedin.com/in/dr-john-campbell-5256223b

Twitter: https://twitter.com/Johnincarlisle

December 24, 2024 Posted by | Science and Pseudo-Science, Video | , | Leave a comment

Let’s Retire Overused Words. First, ‘Misinformation’

By Dr. Pierre Kory & Mary Beth Pfeiffer | Real Clear Health | December 16, 2024

In a seismic political shift, Republicans have laid claim to an issue that Democrats left in the gutter—the declining health of Americans. True, it took a Democrat with a famous name to ask why so many people are chronically ill, disabled and dying younger than in 47 other countries. But the message resonated with the GOP.

We have a proposal in this unfolding milieu. Let’s have a serious, nuanced discussion. Let’s retire labels that have been weaponized against Robert F. Kennedy Jr., nominated for Health and Human Services Secretary, and many people like him.

Start with discarding threadbare words like “conspiracy theory,” “anti-vax,” and the ever-changing “misinformation.”

These linguistic sleights of hand have been deployed—by government, media and vested interests—to dismiss policy critics and thwart debate. If post-election developments tell us anything, it is that such scorn may no longer work for a population skeptical of government overreach.

Although RFK has been lambasted for months in the press, he just scored a 47 percent approval rating in a CBS poll.

Americans are asking: Is RFK on to something?

Perhaps, as he contends, a 1986 law that all-but absolved vaccine manufacturers from liability has spawned an industry driven more by profit than protection.

Maybe Americans agree with RFK that the FDA, which gets 69 percent of its budget from pharmaceutical companies, is potentially compromised. Maybe Big Pharma, similarly, gets a free pass from the television news media that it generously supports. The U.S. and New Zealand, incidentally, are the only nations on earth that allow “direct-to- consumer” TV ads.

Finally, just maybe there’s a straight line from this unhealthy alliance to the growing list of 80 childhood shots, inevitably approved after cursory industry studies with no placebo controls. The Hepatitis B vaccine trial, for one, monitored the effects on newborns for just five days. Babies are given three doses of this questionably necessary product—intended to prevent a disease spread through sex and drug use.

Pointing out such conflicts and flaws earns critics a label: “anti-vaxxer.”

Misinformation?

If RFK is accused of being extreme or misdirected, consider the Covid-19 axioms that Americans were told by their government.

The first: The pandemic started in animals in Wuhan, China. To think otherwise, Wikipedia states, is a “conspiracy theory,” fueled by “misplaced suspicion” and “anti-Chinese racism.”

Not so fast. In a new 520-page report, a Congressional subcommittee linked the outbreak to risky U.S.-supported virus research at a Wuhan lab at the pandemic epicenter. After 25 hearings, the subcommittee found no evidence of “natural origin.”

Is the report a slam dunk? Maybe not. But neither is outright dismissal of a lab leak.

The same goes for other pandemic dogma, including the utility of (ineffective) masks, (harmful) lockdowns, (arbitrary) six-foot spacing, and, most prominently, vaccines that millions were coerced to take and that harmed some.

Americans were told, wrongly, that two shots would prevent Covid and stop the spread. Natural immunity from previous infection was ignored to maximize vaccine uptake.

Yet there was scant scientific support for vaccinating babies with little risk, which few other countries did; pregnant women (whose deaths soared 40 percent after the rollout), and healthy adolescents, including some who suffered a heart injury called myocarditis. The CDC calls the condition “rare;” but a new study found 223 times more cases in 2021 than the average for all vaccines in the previous 30 years.

Truth Muzzled? 

Beyond this, pandemic decrees were not open to question. Millions of social media posts were removed at the behest of the White House. The ranks grew both of well-funded fact-checkers and retractions of countervailing science.

The FDA, meantime, created a popular and false story line that the Nobel Prize-winning early-treatment drug ivermectin was for horses, not people, and might cause coma and death. Under pressure from a federal court, the FDA removed its infamous webpage, but not before it cleared the way for unapproved vaccines, possible under law only if no alternative was available.

An emergency situation can spawn official missteps. But they become insidious when dissent is suppressed and truth is molded to fit a narrative.

The government’s failures of transparency and oversight are why we are at this juncture today. RFK—should he overcome powerful opposition—may have the last word.

The conversation he proposes won’t mean the end of vaccines or of respect for science. It will mean accountability for what happened in Covid and reform of a dysfunctional system that made it possible.

Dr. Pierre Kory, M.D., a pulmonologist and critical care specialist, is president emeritus of the FLCCC Alliance. Mary Beth Pfeiffer is an investigative reporter and author.

December 21, 2024 Posted by | Civil Liberties, Corruption, Deception, Fake News, Full Spectrum Dominance, Mainstream Media, Warmongering, Science and Pseudo-Science | , , , | Leave a comment

Documents Show CISA Monitored and Influenced Domestic Speech on COVID-19 Through Private Sector Partners

Private entities were enlisted to flag content, even accurate information.

By Didi Rankovic | Reclaim The Net | December 20, 2024

America First Legal (AFL) has revealed new information from a document it has been able to obtain through the lawsuit filed against the Cybersecurity and Infrastructure Security Agency (CISA).

CISA is part of the US Department of Homeland Security (DHS), which has a “foreign disinformation” unit, the Countering Foreign Influence Task Force (CFITF).

However, as early as mid-February 2020, CISA (via CFITF) had already started to monitor domestic speech about Covid – nearly a month before the pandemic was officially declared by the UN’s WHO, and before orders started to be issued to shut down schools and businesses in the US.

Even though several layers deep, CFITF was still a government entity, and in order to circumvent constitutional issues related to censorship of online speech, the document indicates that the unit turned to what AFL brands “the censorship industrial complex” – specifically, its private sector component.

These were “fact checkers,” “bias raters” and similar that keep cropping up in revelations about the Covid-era censorship: Atlantic Council DFR Lab, Media Matters, Stanford Internet Observatory, Alliance for Securing Democracy, Center for Countering Digital Hate (CCDH) (a UK-based group, which now passes as “British-American”), Global Disinformation Index (GDI), and even an openly foreign government project, EU’s “EU vs. Disinfo.”

Among the kinds of speech CFITF would monitor and/or flag was that of President Trump, his comments about Hydroxychloroquine going back to 2020. The document reveals that CFITF (via Atlantic Council, DFR Lab) knowingly chose to give itself the right to flag even accurate information, justifying a thing as serious as censorship by presenting hypothetical scenarios:

“Once-accurate information can become misinformation as it ages, leading to erroneous conclusions and misinterpretation of the current situation,” the document reads. This was put in the context of the rapidly changing “nature” of the pandemic.

However, it took years for the same awareness – that information related to Covid was constantly changing – to start reversing some censorship decisions (e.g., the Covid origin theory).

As for CISA/CFITF early pandemic activities affecting online speech, AFL believes that they may represent “a violation of what’s known as the Supreme Court’s ‘major questions’ doctrine, which holds that government agencies must not stray from the specific legal authorities given to them by Congress.”

December 20, 2024 Posted by | Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science | , , , | Leave a comment

Pfizer mRNA ‘Vaccinated’ Children Significantly More Likely to Get COVID-19 Than Unvaccinated Peers

By Nicolas Hulscher, MPH | Courageous Discourse | December 16, 2024

A new study was just published in the Journal of the Pediatric Infectious Diseases Society titled, Protection from COVID-19 vaccination and prior SARS-CoV-2 infection among children aged 6 months – 4 years, United States, September 2022–April 2023. The study combined data from three prospective cohort studies (PROTECT, CASCADIA, and CoVE) conducted in the United States from September 1, 2022, to April 30, 2023. Included 614 children aged 6 months to 4 years living in Washington, Oregon, Michigan, Arizona, and Utah.

Here are the key findings:

  1. Increased Risk with Pfizer-BioNTech Vaccination:
    • Children vaccinated with Pfizer-BioNTech without prior SARS-CoV-2 infection were 159% more likely to get infected and 257% more likely to develop symptomatic COVID-19 compared to unvaccinated children without prior infection:
      • Hazard Ratio (HR) for infection: 2.59 (95% CI: 1.27–5.28).
      • HR for symptomatic COVID-19: 3.57 (95% CI: 1.10–11.63).
  2. Prior Infection Offers Robust Protection:
    • Children with prior SARS-CoV-2 infection (unvaccinated) had a significantly lower risk of reinfection compared to unvaccinated, infection-naïve children:
      • HR for infection: 0.28 (95% CI: 0.16–0.49).
      • HR for symptomatic COVID-19: 0.21 (95% CI: 0.08–0.54).
  3. No Protective Effect from Vaccination Alone:
    • There was no significant reduction in the risk of infection or symptomatic COVID-19 for vaccinated children (Moderna or Pfizer-BioNTech) compared to unvaccinated children:
      • HR for infection with vaccination alone: 1.23 (95% CI: 0.69–2.16).
      • HR for symptomatic COVID-19 with vaccination alone: 1.61 (95% CI: 0.65–4.03).
  4. Boosters Show No Significant Protection:
    • Among children who received at least one bivalent booster dose, there was no significant reduction in infection or symptomatic COVID-19:
      • HR for infection with a bivalent booster: 0.74 (95% CI: 0.37–1.48).
      • HR for symptomatic COVID-19 with a bivalent booster: 1.04 (95% CI: 0.37–2.96).

In other words, these injections do the opposite of what they’re supposed to do. Instead of protecting against COVID-19, these genetic injections either fail or increase the risk. The CDC should immediately revoke their recommendations for children aged 6 months and older to receive a COVID-19 booster injection.


Nicolas Hulscher, MPH

Epidemiologist and Foundation Administrator, McCullough Foundation

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