Tag: bird flu

USDA Orders Raw Milk Testing Under Guise Of Bird Flu Amid War On Small Farms

Nationwide demand for raw milk has never been higher, as out-of-control bureaucrats in their ivory towers in Washington, DC, exploit bird flu outbreaks in dairy herds to financially crush small farms while ensuring that large-scale farms owned by mega corporations, which produce questionable/unhealthy food (hence America’s obesity crisis), remain in control of the nation’s food supply chain.

The latest overreach in the war on raw milk comes as the US Department of Agriculture (USDA) ordered dairy farmers to work with the federal agency to test for bird flu (H5N1).

On Friday, USDA Secretary Tom Vilsack wrote in a statement, “This new milk testing strategy will build on those steps to date and will provide a roadmap for states to protect the health of their dairy herds.”

“Among many outcomes, this will give farmers and farmworkers better confidence in the safety of their animals and ability to protect themselves, and it will put us on a path to quickly controlling and stopping the virus’ spread nationwide,” Vilsack said.

The new testing mandate gives the federal government yet another foothold in controlling the nation’s milk supply and moves one step closer to banning raw milk, all under the guise of combating “bird flu.”

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Bird Flu: The “Next Pandemic” is right on schedule

We haven’t published anything about bird flu since June. There hasn’t been much to say. Nevertheless, I still regularly comb through journals and news sites, ensuring we don’t miss anything potentially important.

During one such search yesterday evening I found this article in the journal Science, its title asking simply:

Why hasn’t the bird flu pandemic started?

…and, you know what, that’s a good question. Why hasn’t the bird flu pandemic started?

Not literally, of course. The bird flu “pandemic” won’t ever really start. If or when it is declared it will be a lie, just like Covid.

The question is why haven’t they started the big roll out yet?

That is obviously the plan after all.

The establishment has been signposting “the next pandemic” since before Covid sidled off the world stage. “Pandemic preparedness” has been a buzz phrase at all the intergovernmental panels and UN summits for at least two years. All the indications were that bird flu was the anointed successor.

But it’s all come to nothing so far.

Bird flu hasn’t become “the next pandemic”, it hasn’t become really anything at all, it’s barely even grazed the major news cycle.

Instead, the story has been stuck in a strange holding pattern, circling around with dire warnings of imminent danger, only to swoop away from the runway before its wheels touch down.

A pot that never boils despite the fact nobody’s really watching.

Why hasn’t the bird flu pandemic happened yet? What are they waiting for?

Well, Donald Trump, apparently, amongst other things.

That’s isn’t speculation, it’s definite messaging. It looks as if some sort of narrative about Trump failing to do enough, or the right things to handle the “crisis” might be in the offing.

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FDA approves Gates-backed bird flu vaccine trial: ‘Disaster waiting to happen’

The FDA has approved the first phase of human trials for a self-amplifying mRNA bird flu vaccine developed by Arcturus Therapeutics, funded by the US government and the Gates Foundation. This vaccine, targeting the H5N1 virus, introduces an enzyme prompting cells to produce more mRNA, leading to sustained antigen production, which experts warn could lead to prolonged immune activation and unknown health risks.

Epidemiologist Dr. Nicolas Hulscher described the FDA’s approval as an opportunity for Arcturus to “experiment with injecting humans with H5N1 bird flu replicon mRNA.” The clinical study is funded by the Biomedical Advanced Research and Development Authority (BARDA), a division of HHS focused on pandemic preparedness. Arcturus also recently received a $928,563 grant from the Gates Foundation, which has long supported mRNA research.

Arcturus claims self-amplifying mRNA vaccines can provide immunity with smaller doses. However, Hulscher warned that even a small dose might be more hazardous due to the vaccine’s self-replicating nature, as the extent of antigen production cannot be precisely measured or controlled.

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Arcturus Therapeutics is seeking approval from the FDA to go ahead with self-replicating bird flu vaccine trials

Self-amplifying RNA (“saRNA”), also termed self-replicating RNA (“srRNA”), and self-amplifying mRNA (“sa-mRNA” or “samRNA”) are synonymous terms. Both refer to a synthetic mRNA molecule engineered to replicate itself within host cells.  Vaccines using this self-replicating technology are also called “replicon” vaccines.

In November 2023, Japan approved the use of the first saRNA vaccine against covid.  The vaccine is called Kostaive and is also known as ARCT-154 or, in Vietnam, VBC-COV19-154. It is a CSL and Arcturus Therapeutics vaccine.  At the time of the approval, researchers were hopeful that this was only the beginning for saRNA treatments for infectious diseases and even cancers.  The vaccine, which the Japanese are referring to as the “third atomic bomb,” began to be rolled out in Japan in October 2024 as part of its autumn covid vaccination programme.

There is only explicit mention of Kostaive using STARR mRNA technology. However, it is likely that the Kostaive “vaccine” uses both of Arcturus Therapeutics’ proprietary technologies: STARR (self-transcribing and replicating RNA) mRNA technology and LUNAR (lipid-mediated universal RNA delivery) delivery system.

LUNAR is a nanoparticle delivery system that enables the efficient and targeted delivery of mRNA to cells. STARR is a self-replicating RNA platform that combines with LUNAR to drive “therapeutic” protein expression.

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FDA Greenlights New Bill Gates-Funded ARCT-2304 Self-Replicating samRNA ‘Pandemic’ H5N1 Bird Flu Jab

Arcturus Therapeutics, a company specializing in mRNA-based pharmaceuticals, quietly announced Monday that the U.S. Food and Drug Administration (FDA) has granted approval for its Investigational New Drug (IND) application for ARCT-2304, a self-amplifying mRNA (sa-mRNA) injection targeting the H5N1 avian influenza “bird flu” virus.

The FDA has recently come under fire for “failing to meet safety requirements” and “failing to prioritize scientific data quality delivered from FDA laboratories,” according to the U.S. House of Representatives Committee on Energy and Commerce.

The new Arcturus trial, funded by the Biomedical Advanced Research and Development Authority (BARDA), aims to assess ARCT-2304’s efficacy in preventing pandemic influenza and plans to enroll around 200 healthy adults across the United States.

“Arcturus is actively engaged with the U.S. government to prepare for the next pandemic, and clearance to proceed into the clinic with our STARR® self-amplifying mRNA technology is a key step in this important process,” said Joseph Payne, President & CEO of Arcturus Therapeutics in a press release.

“The Phase 1 clinical trial is designed to evaluate the safety, reactogenicity, and immunogenicity of ARCT-2304 as a potential vaccine to protect against the highly pathogenic H5N1 avian influenza.”

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H5N1 Avian Flu: What You Need to Know

Over the last four years the medical-financial-military complex has demonstrated its ruthlessness. The COVID-19 operation, revealed viral bio-weapons labs and research a.k.a. “gain of function”. It also revealed nefarious tactics including suppressed treatments, destructive mandates,  misleading PCR test programs, scaremongering, propaganda, and dangerous genetic injections coerced into the worlds’ population under false pretenses of “safe and effective vaccines” for COVID-19.

Despite how blatantly criminal that is, and how hard we continue working to bring the perpetrators to justice; many of them are still holding high offices,  and emboldened with more money and power ill-gotten through the COVID-19-crimes-against-humanity. We would be foolish not to watch the WHO and its accomplices’ actions now with very critical and defensive thinking.

There are two current major sequels to COVID-19. They are both active operations being executed against us now by the same medical-financial-military complex. These are H5N1 avian flu, and monkey-pox. Here I will tackle H5N1 avian flu in detail.

I hope that this article will provide important knowledge and wisdom; to help minimize the destructive impact of the current H5N1 avian flu operation.

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BIRD FLU: They Fooled Us Once. Looks Like They’ll Try to Fool Us Again.

The more we learn about the made-up rules enforced during the COVID-19 pandemic, the more outrageous the entire thing becomes. Anthony Fauci had the utter audacity to sit in Congress and admit they had no data, so they just creatively improvised things like social distancing measures. They fooled a lot of folks once, so shame on them. It looks like they’re about to try and fool us twice with the Bird Flu. If we fall for it again, then shame on us.

They did everything from withholding effective medications to depriving people of employment to shaming people publicly, discriminating against them, and wishing them dead.

Then as if 2020 and 2021 weren’t brutal enough, we find out from Congressional investigations and Anthony Fauci’s recent testimony it was all a bunch of baloney to make Big Pharma rich and Big Government powerful. People died who didn’t need to die, the elderly became isolated from their loved ones, medical personnel became burned out and traumatized, and children lost an entire year of educational experiences. Others were vaccinated, some eagerly and some grudgingly, and are suffering long-term disability and even death from the hastily created mRNA vaccine.

If we don’t take away some lessons from this, we don’t deserve to call ourselves preppers.

And it looks like we’re about to be tested on what we’ve learned.

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Colorado Governor Declares Disaster Emergency Over Bird Flu Outbreak

Colorado Gov. Jared Polis issued an emergency disaster declaration in his state over an outbreak of highly pathogenic bird flu in northeastern Weld County as officials recently reported that 1.8 million chickens were impacted by the virus.

The governor “verbally” declared a disaster after “an avian flu outbreak in a commercial poultry facility in Weld County,” according to a news release from his office issued on Monday. Mr. Polis’s office did not name the facility that was impacted by the outbreak.

The declaration means that Colorado can use its emergency powers to “take all necessary and appropriate state actions to assist with response, recovery, and mitigation efforts.”

In an update issued on July 8, the Colorado Department of Agriculture confirmed that 1.78 million chickens were impacted by highly pathogenic avian influenza.

The Colorado Department of Public Health and Environment said in a statement on July 3 that a dairy farm worker in northeastern Colorado was infected with the H5N1 bird flu and had direct exposure to cattle infected with the virus. His only symptom was conjunctivitis, colloquially known as pink eye, which was described by the agency as mild.

“He has recovered. This case is an employee at a dairy farm in northeast Colorado who had direct exposure to dairy cattle infected with avian flu. To protect patient privacy, additional details are not being provided,” the agency said last week in a news release.

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NewsGuard fact-checked me today, providing the opportunity to clarify questions about the Audenz vaccine and the extremely high mortality rate in its small trial.

The big guns, the Health Editor, approached me this afternoon. Happy to learn the presentation is getting attention.

Below is the email I received and below that is my detailed reply.

On Jul 3, 2024, at 1:26 PM, John Gregory <john.gregory@newsguardtech.com> wrote:

Dr. Nass, 

My name is John Gregory, health editor at NewsGuard. We’re a news organization that reports on and tracks online misinformation. 

I’m emailing in regards to your April 20, 2024, CHD video in which you cited the FDA package insert for the H5N1 vaccine Audenz, and said, “One in 200 people who got this vaccine in a clinical trial died,” and later added, “This is a dangerous vaccine for a nothing disease.”

Video of your remarks has begun circulating widely on social media platforms in the past two weeks, used as evidence for claims like “Dr. Meryl Nass: One of the approved Bird Flu quackccines, Audenz… had a death rate of 1 in 200 during clinical trials.” 

I noticed the screenshot included in your original video highlighted the sentence, ““Fatal SAEs [Serious Adverse Events] included 11 (0.5%) Audenz recipients and 1 (0.1%) placebo recipients,” even though the very next sentence said, ““No SAEs were assessed as being related to Audenz,” meaning that none of the reported serious adverse events – including deaths – that occurred among trial participants were caused by the vaccine.

You also did not mention that the FDA’s own statistical review of Audenz stated that, “No deaths occurred that were considered related to the vaccine,” and concluded, “No major statistical or safety issues have been identified” with the vaccine, or that the published results of the Audenz trial said:

None of the serious AEs or AEs of special interest reported by subjects who received aH5N1c were considered vaccine related. Two subjects in the placebo group reported a related AE of special interest (immune thrombocytopenic purpura and polymyalgia rheumatic); these events were also considered serious AEs. During the study, 12 (0.4%) subjects had serious AEs with a fatal outcome, none of which were attributed to the study treatment, and most (n = 11) occurred after Day 43 during the follow-up period in subjects ≥65 years with underlying severe comorbidities and multiple concomitant medications.

Is there any reason why you did not mention any of this countervailing information?

My deadline is 5pm eastern today, July 3. Thank you. 

— 

Best regards, 
John Gregory

john.gregory@newsguardtech.com

Office: ‪(312) 489-8676

More about NewsGuard criteria here.

Dear Mr. Gregory,

Since I provided a screenshot of the package insert of the Audenz licensed vaccine and repeated what it said, this can hardly be characterized as misinformation, which you claim to be investigating.  Since I included the next sentence in the presentation, it cannot even be construed as incomplete.

Had you been working on issues of vaccines for over 25 years as I have, you would have been aware that the sponsor (mfr) and FDA, who together craft the vaccine labels aka package inserts, ALWAYS assert that most or all of the deaths and serious adverse events occurring during a clinical trial were adjudged to be not due to the vaccine.  Had they judged otherwise, a license would probably not have been issued.  A license was issued for Audenz.

Later, when a vaccine is given to millions of people, not just a few hundred as in this case, one learns which side effects are IN FACT attributable to the vaccine.

For example, at least a hundred million Americans had received an mRNA COVID vaccine before it was determined to cause myocarditis, in late May of 2021 by FDA.

That is the reason why the raw data, which I presented, are important.  So that people have the information to judge for themselves what risks they may face when choosing vaccination.  In fact, clinical trials often exclude sick subjects, and drugs and vaccines almost invariably appear more safe and effective in clinical trial data than they do later, in the real world—a fact known to all medical researchers.

Why did I not mention material from an article?  Because I was referring to the Audenz label, which is the legal document that FDA attests is true, unlike published articles which are generally written by the vaccine sponsor and have a lesser degree of reliability.  In fact, the numbers in the article versus those in the label are not exactly the same.

Furthermore, if the US government was comfortable with the H5N1 Audenz vaccine, why did DHHS’ BARDA just place an order with Moderna for H5N8 mRNA vaccines, even though the avian flu circulating in the US is H5N1?  Even though it makes much more sense to match the neuraminidase portion of the vaccine to the circulating strain…  which is done every year when seasonal influenza vaccines are produced?

Finally, I invite you to take a look at the WHO data on deaths in humans worldwide from the H5N1 bird flu, which confirms it is a nothing disease in humans, having mutated to a different form than it once had.  The federal health agencies have monitored 9,000 farm workers and all they found were 4 mild cases of disease, no hospitalizations and no deaths in the US over the past several years.

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U.S. Will Pay Moderna $176 Million to Develop mRNA Bird Flu Vaccine

The United States government will pay vaccine manufacturer Moderna $176 million to develop a new mRNA vaccine to treat bird flu.

The U.S. Department of Health and Human Services will pay Moderna $176 million for a vaccine containing the same mRNA technology as the company’s COVID-19 vaccine.

Bird flu, or H5N1, has been reported in dairy cows and has infected three people in the United States.

In total, 135 dairy herds have been infected with bird flu in 12 states.

Per AP:

The U.S. government will pay the vaccine maker Moderna $176 million to develop a pandemic vaccine that could be used to treat bird flu in people as cases in dairy cows continue to mount across the country, federal officials announced Tuesday.

The funds are targeted for release through the U.S. Department of Health and Human Services and will pay for continued development of a vaccine that uses the same mRNA technology that allowed rapid development and rollout of vaccines to protect against COVID-19. The award was made through the Biomedical Advanced Research and Development Authority, or BARDA, a program focusing on medical treatments for potential pandemics.

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