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Health

Dr. Malone: Bird flu ‘emergency’ in California is a case of psychological bioterrorism

Published

2 months ago

8 minute read

From LifeSiteNews

By Robert Malone M.D.

Contrary to initial reporting from corporate media, the WHO, and the apocalyptic mutterings of Dr. Peter Hotez, there continues to be no evidence indicating the circulation of a highly pathogenic version of bird flu in either animal or human populations.

What is the current threat assessment for Avian Influenza, and has it changed?

I previously established and published a brief baseline threat assessment for Avian Influenza on July 2, 2024. Four dominant parameters must be considered when assessing a potential infectious disease threat to human populations:

  1. Disease severity (a measurable objective truth)
  2. Mechanism of transmission and observed transmissibility (an experimentally testable objective truth)
  3. Evidence of sustained human-to-human transmission (a measurable objective truth)
  4. Assessment of anticipated future risk (subjective, speculative, and hypothetical)

An assessment of the conflicts of interest and political agenda(s) of California’s Gavin Newsom is beyond the scope of this analysis. Still, please remember that Governor Newsom clearly mismanaged and overreacted to the COVID threat, as did the World Economic Forum that trained and coached (coaches?) him as a “Young Leader” and clearly continues to influence his political postures.

Although California has remained under Democrat party control – in significant part consequent to “rank choice” voting policies – during the recent presidential election there was a clear shift and momentum toward the Republican party across the majority of the state.

California has a very large dairy industry, and I know that a leader in and representative of that industry has close connections to Newsom. The presence of the virus in Southern California dairy farms is widespread, with over 300 dairy herds testing positive in the last 30 days

Has the threat assessment circa July 2024 changed? Let’s revisit the basics:

Disease severity, December 2024

Disease severity continues to be mild, with the exception of one new case which apparently triggered Newsom to declare a state of emergency in California.

According to Newsweek, “A person in Louisiana was hospitalized in critical condition with severe respiratory symptoms from a bird flu infection, according to state health officials. The patient had been in contact with sick and dead birds in a backyard flock, according to the CDC. Louisiana health officials said the patient is older than 65 and has underlying medical conditions.”

Here is the current CDC threat summary

  • H5 bird flu is widespread in wild birds worldwide and is causing outbreaks in poultry and U.S. dairy cows with several recent human cases in U.S. dairy and poultry workers.
  • While the current public health risk is low, CDC is watching the situation carefully and working with states to monitor people with animal exposures.
  • CDC is using its flu surveillance systems to monitor for H5 bird flu activity in people.

The CDC charts above document that the risk of H5 in humans is low, disease severity is low, and although massive testing has occurred, there are only 61 total “exposure” sources found from cattle, birds, and other mammals.

There are a total of three human cases picked up from the CDC flu surveillance program since February 25, 2024, and a total of 58 cases in the U.S., after testing almost 10,000 people who were exposed to infected animals.

In sum, the profile of disease severity has not changed since July 2024. As opposed to initial reporting from corporate media, dark warnings from the WHO and Dr. Tedros, and the apocalyptic mutterings of Dr. Peter Hotez, there continues to be no evidence indicating the circulation of a highly pathogenic version of this virus in either animal or human populations.

Mechanism of transmission and observed transmissibility

All reported U.S. transmission events involve human exposure in the context of intensive contact during animal husbandry or other known animal hosts, indicating that the mechanism of transmission remains intensive exposure to infected animals and animal carcasses. No change from July 2024.

Evidence of sustained human-to-human transmission

No evidence of sustained human-to-human transmission, now or in the past with this currently circulating variant.

Assessment of anticipated future risk

This appears to be the crux of Newsom’s alarmist response involving the declaration of a “State of Emergency” for bird flu in California. A statement from the governor’s office characterized the move as a “proactive action to strengthen robust state response” to avian influenza A (H5N1), also known as bird flu.

“This proclamation is a targeted action to ensure government agencies have the resources and flexibility they need to respond quickly to this outbreak,” Newsom said in a statement. “Building on California’s testing and monitoring system – the largest in the nation – we are committed to further protecting public health, supporting our agriculture industry, and ensuring that Californians have access to accurate, up-to-date information.”

He added, “While the risk to the public remains low, we will continue to take all necessary steps to prevent the spread of this virus.”

This statement demonstrates either a profound ignorance of the mechanism by which animal influenza viruses spread, including avian influenza, or the presence of a hidden agenda. With a wide range of animal reservoirs, including migratory waterfowl, there is no way that the state of California can prevent the spread of this virus.

READ: Australian doctor who criticized COVID jabs has his suspension reversed

Conclusion

There has been no significant change in the current threat assessment associated with Avian Influenza relative to July 2024. The CDC, which has recently been implicated in industrial-scale “PsyWar” deployment of psychological bioterrorism regarding COVID and has an organizational conflict of interest in promoting vaccines and vaccine uptake, characterizes the current public health risk as low.

My conclusion regarding the Newsom declaration of a “State of Emergency” for bird flu in California is that it is being driven by a hidden agenda. There are multiple hypotheses regarding what that hidden agenda may be, but Newsom’s statement that, “Building on California’s testing and monitoring system – the largest in the nation – we are committed to further protecting public health, supporting our agriculture industry, and ensuring that Californians have access to accurate, up-to-date information,” suggests that this declaration may, at a minimum, reflect advocacy by and for California’s infectious disease testing industry, which includes both academic and commercial components.

Reprinted with permission from Robert Malone.

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Addictions

“Unscientific and bizarre”: Yet another Toronto addiction physician criticizes Canada’s “safer supply” experiment

Published on February 28, 2025

By

By Liam Hunt

“It seems to be motivated by a very small, vocal, and well-connected group of advocates” says Dr. Michael Lester

Dr. Michael Lester, a Toronto-based addiction physician with 30 years of experience, says Canada’s “safer supply” programs are “inherently dangerous” and causing “dystopian” community harms due to widespread fraud.

These programs claim to reduce overdoses and deaths by distributing free addictive drugs—typically 8-milligram tablets of hydromorphone, an opioid as potent as heroin—to dissuade addicts from consuming riskier street substances. Yet experts across Canada say recipients regularly divert (sell or trade) their safer supply on the black market to acquire stronger illicit drugs, which then fuels addiction and organized crime.

“I have a couple dozen patients in my practice who were drug-free prior to the advent of safe supply, and they’ve gone back to using opioids in a destructive way because of the availability of diverted hydromorphone,” said Lester. “Every single day that I go to work, people tell me they’re struggling with the temptation not to take diverted safe supply. They don’t want to take it, but they take it anyway just because it’s cheap and available.”

After safer supply programs became widely accessible across Canada in 2020, Lester’s patients reported an influx of 8-milligram hydromorphone tablets on the black market, coinciding with a crash in the drug’s street price from $15–$20 per pill to just $2. He now estimates that 80 percent of his patients struggling with opioid addiction have relapsed due to diverted safer supply, leading some to abandon treatment entirely.

“Even if it’s sold at the rock-bottom price of $2 or $3 a pill, a person would make tens of thousands of dollars a year, which would have a tremendous impact on their ability to buy other drugs,” he explained. “Selling hydromorphone is too tempting not to do it, which keeps them entrenched in the whole world of dealing with opioid users and having opioids in their premises.”

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Lester said safer supply is evidently “fueling organized crime” because drug seizures in Ontario now commonly include hydromorphone, “which wasn’t happening before.” He added that some individuals who try these diverted drugs later transition to stronger opioids, such as fentanyl.

In July, for example, the London Police Service announced that seizures of hydromorphone had increased by more than 3,000 percent in the city since 2020. According to London Police Chief Thai Truong, “Diverted safer supply is being resold into our community. There’s organized drug trafficking at the highest levels of organized crime, and there’s drug trafficking at the street level. We’re seeing all of it.”

While Lester acknowledges that safer supply can be useful as a “treatment of last resort, after traditional treatments have been tried and failed,” he said it is now being offered immediately to a wide variety of patients, which has “decimated” uptake of traditional addiction therapies, such as methadone and Suboxone.

As a result, conventional addiction clinics are now at risk of shutting down, meaning some communities could lose access to gold-standard treatments (i.e., methadone and Suboxone) while highly profitable, but unscientific, safer supply programs take over instead.

Lester said the evidence supporting safer supply is biased and “misleading” because, generally speaking, these studies simply interview enrolled patients and ask them to self-report whether they benefit from the programs. He noted that many safer supply researchers are public health academics, not doctors, meaning they lack clinical experience with the communities they study.

“It seems to be motivated by a very small, vocal, and well-connected group of advocates that has completely changed the landscape in addiction medicine treatment in a very short time,” he said.

Lester argues that some safer supply researchers seem to purposefully design their study methodologies to favor the programs and disregard systemic harms. He said this flawed science is then propagated by credulous journalists who fail to adequately scrutinize agenda-driven research.

While he personally knows “a couple dozen” colleagues in addiction medicine who regularly express skepticism about safer supply, many have been reluctant to speak out, fearing backlash from activist groups that “terrorize” critics.

“The stories are common of people being harassed and insulted on social media. We’ve heard of doctors being threatened [and] dropped from committees because they spoke out.”

For example, after Lester and his colleagues published two open letters criticizing safer supply in late 2023, they were targeted by a series of articles by Drug Data Decoded, a popular Canadian harm reduction Substack, which compared the doctors to Nazis and eugenicists. The articles were then widely shared on social media by safer supply activists.

Lester recalled an incident in which harm reduction activists targeted a doctor’s daughter at her high school in retaliation for her parent’s public criticism of safer supply.

“It’s just something that seems so unscientific and so bizarre in medicine,” he said. “Physicians just aren’t used to a powerful political lobby changing a treatment protocol.”

After Lester and more than a dozen of his colleagues wrote several public letters calling for reform and requested a meeting with Ya’ara Saks, the federal Minister of Mental Health and Addictions, they found themselves “sidelined and ignored.”

After months of delays, they were able to present their clinical observations to Saks, only to have her disregard them and incorrectly claim, weeks later, that criticism of safer supply is rooted in “fear and stigma.”

“The insults aren’t a big enough consequence to keep me from speaking my mind,” he declared.

After a short reflection, he then added, “If anyone doesn’t have a stigma against this population, it’s me. I’ve dedicated my life to helping them.”

Liam Hunt is a Canadian writer and journalist with an interest in humanism, international affairs, and crime and justice. This story is produced by the Centre For Responsible Drug Policy’s “Experts Speak Up” series in partnership with the Macdonald-Laurier Institute.

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COVID-19

RFK Jr. pauses $240 million contract for new ‘oral COVID vaccine’

Published on February 27, 2025

By

From LifeSiteNews

By Doug Mainwaring

For his first major action since taking office just two weeks ago, Department of Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. has issued a 90-day stop-work order to American biotech company Vaxart Inc., which had been contracted during the Biden administration to develop a new “oral COVID-19 vaccine.”  

Kennedy’s order came just as 10,000 individuals were scheduled to begin clinical trials on Monday.   

HHS will utilize the 90-day hiatus to review Vaxart’s initial findings to determine the future of the human trials and continued drug development.   

Approximately $460 million had been allotted to Vaxart by HHS to develop its new COVID-19 “vaccine,” of which $240 million had been authorized for the preliminary study, according to a report by Fox News Digital, which broke the story.    

“While it is crucial that the Department [of] Health and Human Services support pandemic preparedness, four years of the Biden administration’s failed oversight have made it necessary to review agreements for vaccine production, including Vaxart’s,” Kennedy told Fox News Digital.

“I look forward to working with Vaxart and medical experts to ensure this work produces safe, effective, and fiscal-minded vaccine technology,” added Kennedy.  

“If anyone was worried that RFK would not address vaccine damage, this is proof he’s only getting started,” declared the producers of the 2022 Died Suddenly film, which questioned the motives behind the development and mandating of the first round of COVID-19 shots and the startling number of deaths attributed to them. 

There appears to be plenty of justification for pausing and even terminating Vaxart’s continued development of its “oral COVID-19 vaccine”

According to a report by The Defender’s John-Michael Dumais and published by LifeSiteNews in June, “Vaxart’s pill, VXA-CoV2-1, uses an adenovirus vector to infect epithelial cells in the lower small intestine. The vaccine delivers the genetic material to create the spike protein. The company boasts that a special coating allows the oral pill to survive the low pH in the stomach.” 

“Johnson & Johnson’s (J&J) and AstraZeneca’s COVID-19 vaccines also used adenovirus vectors,” noted Dumais, who explained:   

The use of J&J’s vaccine was paused in April 2021 due to reports of thrombosis with thrombocytopenia syndrome (TTS), a severe blood clotting disorder. In July 2021, the FDA warned about the risk of Guillain-Barré syndrome with the J&J vaccine after approximately 100 cases were reported among 12.8 million vaccine recipients. With existing doses of the J&J vaccine having expired in May 2023, the vaccine is no longer in use.

AstraZeneca’s COVID-19 vaccine also caused blood clots, resulting in temporary pauses in its use in several countries. With declining demand, it was also removed from the market in May 2023.

Vaxart’s oral COVID-19 development project is part of the Biden administration’s $4.7 billion Project NextGen initiative, launched in 2023 to accelerate the development of new COVID “vaccines.”

Vaxart’s “vaccine” was funded through a contract with the Biomedical Advanced Research and Development Authority (BARDA), which falls under the umbrella of HHS’s Administration for Strategic Preparedness and Response.

The pausing of Vaxart’s COVID-19 “vaccine” development can be seen as Kennedy’s first important move to fulfill his stated mission as HHS secretary. 

Shortly after Robert F. Kennedy Jr. was sworn in as secretary of the Department of Health and Human Services (HHS), President Donald Trump signed an executive order titled Establishing The President’s Make America Healthy Again Commission (MAHA EO) to investigate and address the root causes of America’s escalating health crisis.

Chaired by Kennedy, the commission has four main policy directives to reverse chronic disease: Empower Americans through transparency and open-source data and avoid conflicts of interest in all federally funded health research; prioritize gold-standard research on why Americans are getting sick in all health-related research funded by the federal government; work with farmers to ensure that U.S. food is the healthy, abundant, and affordable; and ensure expanded treatment options and health coverage flexibility for beneficial lifestyle changes and disease prevention.  

The MAHA EO came at a time when many Americans have lost trust in the nation’s healthcare system and are increasingly skeptical as to whether they are receiving honest answers about the causes of the country’s health crisis and how to improve it.

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