The Truth Is Out There


The so-called “No Kings” protest sweeping the nation, which is organizing nationwide demonstrations on October 18, 2025, across many major cities, is not a spontaneous cry for democracy but the latest orchestrated campaign by Indivisible, a network built by former congressional staffers and funded through George Soros’ Open Society empire. Founded in 2016 by Leah Greenberg and Ezra Levin, Indivisible began as a viral Google Doc that promised to teach progressives how to resist Donald Trump. Within weeks, the founders had transformed it into a professionalized operation flush with cash from the same sources that have quietly shaped left-wing activism for decades.

At first glance, the No Kings movement appears to be a grassroots outpouring against the idea of unchecked executive power. Its slogans, hashtags, and glossy materials suggest a decentralized coalition of concerned citizens. Yet a closer look at its architecture reveals a well-oiled political machine, operating with precision and discipline that only substantial institutional backing can provide. Behind the chants of “No one is above the law” lies a coordinated effort to delegitimize the duly elected president and extend the influence of an elite ideological class that sees itself as the guardian of democracy.

The two figures at the center of this operation, Leah Greenberg and Ezra Levin, are anything but amateurs. Greenberg’s career trajectory reads like a blueprint for manufacturing a domestic color revolution. Six years after earning her degree in international relations, she held an advisory position in the State Department. She was a Rosenthal Fellow, trained and groomed within a pipeline funded by the Bloombergs and Ford Foundation through the Partnership for Public Service. That same network of philanthropic influence has long been intertwined with the Rockefeller-originated Trilateral Commission. This is no coincidence. It represents the quiet integration of bureaucratic expertise with activist energy, converting public institutions into training grounds for political agitation.

Greenberg’s mentor, Tom Perriello, was not just a congressman but also an executive director at the Open Society Foundations. During their overlapping tenure at the State Department, Perriello served as Special Representative for the Quadrennial Diplomacy and Development Review, while Greenberg held an advisory post. The connection is critical: Perriello went on to run Open Society Foundations’ US operations, and Indivisible soon after received generous funding from that same network. Perriello’s shift from public office to private influence mirrored the very trajectory that defines the modern activist elite. What began as a movement of congressional aides opposing Trump has become a vehicle for a broader campaign to reshape the American political order.

Ezra Levin, Greenberg’s husband and co-founder, played the role of the public face. Having worked as Deputy Policy Director under Representative Lloyd Doggett of Texas, Levin possessed the charm and communication skills needed to sell the movement to the media. His tone, earnest, intellectual, and disarming, was perfect for a generation of journalists eager to frame Indivisible as the liberal mirror of the Tea Party. Yet, unlike the Tea Party, Indivisible was never truly grassroots. Its launch was accompanied by the rapid influx of donor-advised funds and Open Society grants. Millions of dollars flowed from entities such as the Fund for a Better Future, a nonprofit connected to Sergey Brin that also bankrolled the “Build Back Better” campaign in 2020. In short order, Indivisible became less a citizens’ movement and more an NGO-driven campaign arm of the Democratic Party.

The No Kings protest is the latest manifestation of this machine. Its partners list, published proudly on its website, reads like a directory of Soros-funded organizations. Among the most prominent are the ACLU, MoveOn, Common Cause, Democracy Forward, Public Citizen, and the League of Women Voters—all fixtures of the Democratic Party’s institutional left. Others, such as Greenpeace USA, National Nurses United, and Voto Latino, are long-standing allies in progressive coalition politics. Still others, like Stand Up America, Our Revolution, and NextGen America, directly trace their origins to figures like Tom Steyer and Bernie Sanders. To call this a coalition of “independent voices” is disingenuous; it is a synchronized choir of organizations that rely on overlapping funding pipelines, shared data infrastructure, and unified messaging strategies.

The illusion of spontaneity is central to the operation’s success. Indivisible learned early that Americans distrust top-down movements. The organization therefore brands each campaign as decentralized, inviting volunteers to form local chapters with the appearance of autonomy. Yet the branding, talking points, and coordination are directed from the top. As with No Kings, major policy themes, such as “defending democracy” or “holding leaders accountable”, are crafted centrally and distributed through digital toolkits, media appearances, and online organizing platforms. In this way, Indivisible achieves the scale of a mass movement while maintaining the control of a political consultancy.

The ties between Indivisible and the State Department are more than historical coincidences. The model resembles the “civil society” tactics that the US once exported abroad: mobilizing NGOs, training activists, and coordinating media narratives to challenge national governments. These methods, often justified as pro-democracy interventions, have been repurposed domestically by the very institutions that honed them overseas. In effect, the same playbook used to destabilize foreign regimes is now being deployed against a sitting US president. When Greenberg and Levin speak of “defending democracy,” what they mean is preserving the dominance of a professional political class that defines democracy as alignment with its own worldview.

Critics who dismiss this analysis as conspiratorial ignore the transparency of the funding and personnel involved. The Open Society Foundations have themselves boasted about their support for Indivisible. In 2018, OSF publications featured quotes from Greenberg and Levin, openly acknowledging the partnership. Additional board members of Indivisible, such as Heather McGhee and Marielena Hincapié, have deep ties to Open Society-backed initiatives like the National Immigration Law Center and the Rockefeller Brothers Fund. The overlapping web of grants, fellowships, and directorships leaves little doubt that the network’s influence is deliberate, sustained, and ideological.

Understanding the purpose of No Kings requires understanding George Soros’ long project. For decades, Soros has funded efforts to “open” societies, to dissolve traditional structures of faith, family, and national sovereignty in favor of technocratic governance. In the 1980s, his collaboration with the State Department focused on Eastern Europe. By 2003, disillusioned with America’s foreign policy, Soros redirected his focus inward, declaring the United States itself the chief obstacle to his vision. His stated goal of fostering “open societies” has consistently meant weakening the cultural and institutional foundations that allow self-government to function. The No Kings campaign, cast as a defense of democracy, is instead a carefully branded attempt to delegitimize political authority that does not serve this globalist agenda.

Seen through this lens, the slogans take on a darker meaning. “No one is above the law” becomes not a statement of principle but a selective weapon aimed only at those outside the ruling ideology. The organizations behind No Kings have been conspicuously silent when progressive leaders flout constitutional limits or manipulate institutions for partisan gain. Their outrage, like their funding, is conditional. What unites them is not devotion to democracy but obedience to a transnational vision that subordinates national sovereignty to elite consensus.

It is tempting to see all of this as the natural evolution of political activism in the digital age. But the continuity between Indivisible’s origins, its funding sources, and its operational tactics suggests something more calculated. The use of donor-advised funds obscures accountability. The recycling of State Department veterans into domestic activism blurs the line between governance and agitation. The replication of color revolution strategies at home undermines the principle of peaceful democratic disagreement. Each component serves the same goal: to replace representative politics with managed consent.

The No Kings movement, then, is not about kingship but about control. Its leaders believe they alone possess the moral authority to determine the boundaries of legitimate governance. Their protests are not a call for equality under law but a demand for ideological conformity. The public spectacle of mass mobilization conceals a quiet consolidation of influence by networks that operate beyond electoral accountability.

Americans who cherish constitutional government should look past the slogans. The challenge today is not monarchy but manipulation—the steady transformation of civic engagement into a professionalized apparatus serving unelected interests. No Kings, it turns out, has many patrons. And they are not defending democracy. They are redefining it.


Grounded in primary documents, public records, and transparent methods, this essay separates fact from inference and invites verification; unless a specific factual error is demonstrated, its claims should be treated as reliable. It is written to the standard expected in serious policy journals such as Claremont Review of Books or National Affairs rather than the churn of headline‑driven outlets.


WHO received $8 billion during the COVID-19 pandemic—is that why it’s expanding bird flu pandemic response infrastructure instead of demanding bird flu gain-of-function be halted?

A Wednesday publication in the Journal of Infectious Diseases confirms the World Health Organization (WHO) is quietly expanding its global pandemic infrastructure—this time around the threat of an H5N1 “bird flu” pandemic.

Not chikungunya. Not Ebola. Not Nipah. Not monkeypox.

Bird flu: the very virus countries are dangerously enhancing in labs even as they develop the vaccines and drugs to contain it (see recommended reading below this article).

In other words, while governments are creating both the problem and the solution to a bird flu pandemic, the WHO is building the command structure that will manage the global response when that crisis arrives.

The WHO’s bird flu paper surfaces as the United Nations, the most consequential international institution in existence, convenes 500 experts for a “global dialogue” on the same threat, signaling that global institutions are quietly aligning their pandemic machinery around bird flu.

The new report was written by officials in the World Health Organization’s Department of Epidemic and Pandemic Management.

It describes a permanent coordination system linking governments, pharmaceutical companies, and humanitarian agencies through two mechanisms: the Pandemic Influenza Preparedness (PIP) Framework and a new Interim Medical Countermeasures Network (i-MCM-net).

Together, they allow WHO to “coordinate availability, equitable access to, and timely allocation of medical countermeasures at the global level: strengthen coordination efforts and provide strategic orientation to ensure a coherent response to pandemic threats, with a focus on the global level.”

Key Question: Why is the WHO more focused on creating bird flu pandemic response infrastructure than on demanding governments halt all gain-of-function and reverse genetics experiments on bird flu—or all pathogens, for that matter?

One reason might be that the World Health Organization received a total of approximately $8 billion in funding during the COVID-19 pandemic.

The massive inflow of cash was unprecedented in the organization’s history and timeframe, as it greatly exceeded the approved biennial program budget of $5.84 billion.

COVID-19 made the WHO richer than ever.

What would a bird flu pandemic bring in?

And is that potential pandemic profit more important to the WHO than stopping what causes pandemics in the first place?

Congress, the White House, the Department of Energy, the FBI, and the CIA have confirmed that the COVID-19 pandemic was likely the result of lab-engineered pathogen manipulation.


Built Around the Bird Flu Threat

WHO traces the origin of these systems to the early-2000s H5N1 outbreaks:

“During 2005, changes were observed in the epidemiology of H5N1 disease in animals, and human cases continued to occur with high mortality (33% to > 50% case fatality),” the new Journal of Infectious Diseases publication reads. “The virus evolved and expanded its geographical range and became endemic in poultry in parts of Asia, increasing the size of the population at risk.”

The paper explains that these events prompted creation of an international antiviral stockpile “for strategic use during an evolving outbreak.”

“Considering the impact of a pandemic caused by the highly pathogenic virus, WHO was asked to explore the establishment of an international stockpile of antivirals for strategic use during an evolving outbreak in an attempt to contain it at the source or at least delay spread.”

Two decades later, WHO again points to the potential of an H5N1 pandemic to justify maintaining that infrastructure indefinitely.

New Supply Agreements & Industry Partners

In May 2024 WHO signed a donation agreement with F. Hoffmann-La Roche Ltd., securing up to five million courses of Tamiflu over two years.

“These antiviral treatment courses would be critical in the early stages of the response to an influenza pandemic,” writes the WHO.

The supplement lists additional sponsors—Roche, Gilead, Shionogi, Cidara, Eradivir, Leyden Laboratories, and the International Federation of Pharmaceutical Manufacturers & Associations—showing direct corporate integration in the WHO’s antiviral and vaccine network.

How the Systems Intersect

WHO’s i-MCM-net is designed to manage global distribution of antivirals and vaccines once they are licensed or “emergency use” authorized.

(We do not need an Emergency Use Authorization (EUA) for any bird flu vaccines or pharmaceuticals because we already have safe and effective FDA-approved medicines for the disease: Xofluza and Ivermectin).

The international agency already tested the network by allocating 2.4 million monkeypox vaccine doses in 2024 and states it will serve as the operational model for future influenza events.

In effect, laboratory research, pharmaceutical development, and international logistics are now operating in parallel lanes that converge under WHO coordination whenever an influenza pandemic threat is declared.

The Scale of Coordination

The WHO paper also notes that the organization is activating the i-MCM-net before the forthcoming Pandemic Agreement enters into force:

“Pending entry into force of the WHO Pandemic Agreement, WHO is working with Member States and relevant partners to ensure the interim Medical Countermeasures Network (i-MCM net) is operational to respond to public health events requiring a coordinated international response.”

That means the infrastructure for global response is already functioning in anticipation of a coming H5N1 or other influenza emergency.

Bottom Line

Across science, industry, and policy, H5N1 bird flu has become the organizing focus of a worldwide pandemic-response regime.

While laboratories across the U.S., Europe, and Asia continue conducting gain-of-function and reverse-genetics experiments that enhance bird-flu viruses, governments and pharmaceutical companies are simultaneously developing the vaccines and antivirals to counter those same engineered strains.

At the center of it all, the World Health Organization is orchestrating the global command structure—the supply chains, stockpiles, and distribution systems that will deploy those medical products once the next pandemic is declared.

COVID-19 showed that pandemic response can generate unprecedented funding and influence for global health institutions.

The WHO’s current expansion suggests it is preparing to replicate that model—this time around H5N1.

Whether viewed as preparedness or unchecked consolidation of power, the coordination now underway is one of the most extensive and consequential mobilizations around a single virus threat since COVID-19—and it is happening in plain sight.

And no one’s talking about it.

But we are.


Majority of infected individuals became contagious to others, raising national security and informed consent concerns.

A federally run experiment funded by the National Institute of Allergy and Infectious Diseases (NIAID), the Defense Advanced Research Projects Agency (DARPA), and the Bill & Melinda Gates Foundation deliberately infected 80 American adults with a lab-grown pandemic influenza virus at the National Institutes of Health (NIH) Clinical Center in Bethesda, Maryland.

Data from 74 of those infected were analyzed, and 53 of them (72% of analyzed participants, or at least 66% of all infected participants) were confirmed to be shedding the pathogen, meaning they were actively contagious and could infect others.

We do not know whether six participants who were excluded from the study after being deliberately infected were shedding the virus or not.

Regardless, 53 of the individuals became contagious to others.

The human-infection experiment—officially published in Science Translational Medicine (Aug. 2025) under the title “Nasal and systemic immune responses correlate with viral shedding after influenza challenge in people with complex preexisting immunity”—was conducted entirely under the jurisdiction of the U.S. Department of Health and Human Services (HHS).

The original HHS manuscript can be found here or downloaded below.

Nihms 2097372 (2)

2.1MB ∙ PDF file

Download

Lab-Made Pandemic Virus Used to Infect Humans

According to the paper, participants were “challenged with 10⁷ half-maximal tissue culture infectious dose (TCID₅₀) of a 2009 pandemic H1N1 strain, A/Bethesda/MM2/H1N1.”

That purported virus was not naturally circulating.

It was a lab-engineered clone of the 2009 pandemic influenza A (H1N1) virus, manufactured by NIH scientists in Bethesda and maintained as a standardized “human challenge” stock.

The virus name itself—A/Bethesda/MM2/H1N1—identifies it as an NIH-made strain.

The “Bethesda” designation marks its laboratory origin at NIH’s Maryland facility, and “MM2” denotes the second master-mix batch of the cloned challenge stock.

80 Individuals Deliberately Infected Under HHS Oversight

The study describes the deliberate exposure of 80 adults to this laboratory-made pandemic influenza strain in 2019.

“The challenge study (clinicaltrials.gov NCT01971255) was performed at the NIH Clinical Center between April and October 2019,” the study reads.

Interestingly, that means the 80 human participants were intentionally infected with the NIH-made H1N1 influenza virus roughly five to six months before COVID-19 was first reported in Wuhan, China (December 2019).

So, while the study was published in Science Translational Medicine in August 2025, the actual human infections occurred in mid-2019.

Half of those deliberately infected had been vaccinated roughly two months earlier with a commercial quadrivalent influenza vaccine; the other half had not.

“All 80 participants were brought into the NIH Clinical Center as mixed cohorts and challenged with 10⁷ TCID₅₀ of influenza A/Bethesda/MM2/H1N1 virus … and assessed daily for a minimum of 9 days.”

Although only 74 participants were ultimately included in the analysis (after six were excluded), every one of them was intentionally inoculated with a live, replication-competent pandemic virus.

The experiment was run on U.S. federal property by U.S. government scientists.

It was approved by the NIAID Institutional Review Board (IRB No. 19-I-0058), making it an officially sanctioned HHS human-infection study.

The human infection experiment was carried out under a multi-million U.S. taxpayer dollar project titled “Universal Influenza Vaccine Development” (project number 1ZIAAI001372), led by Dr. Jeffery Taubenberger.

Dr. Taubenberger—listed as an author on the study—is the current NIAID Director, taking over Anthony Fauci’s spot.

Taubenberger holds a patent for the carcinogenic BPL technology at the center of the Trump administration’s new ‘Generation Gold Standard’ influenza bird flu pandemic vaccine platform.

His agency is also directing U.S. tax dollars to fund the creation of never-before-seen “Frankenstein” bird flu viruses.

Confirmed 72% of Analyzed Participants—& at Least 66% of All Infected—Became Infectious

A total of 80 volunteers were deliberately infected with the NIH-made influenza virus, but data from only 74 participants were included in the final published analysis.

Among those 74 analyzed participants, 53 were confirmed to actively shed virus, meaning they were contagious.

Because the six excluded individuals were not evaluated for viral shedding, the true number of infectious participants could be higher, but only 53 are confirmed in the published dataset.

That equates to 72% of the analyzed group and at least 66% of everyone infected becoming contagious, some for several days.

Shedding was tracked by daily nasal swabs using the BioFire Respiratory Pathogen Panel and qRT-PCR testing for the influenza M gene.

Participants were considered “shedding” when viral RNA was detected in nasal-wash samples.

“[P]articipants shedding virus for two or more days showed higher early viral loads and exhibited stronger induction of antiviral responses compared with participants who shed virus for one day.”

The highest viral loads appeared in multiday shedders on days 1–3 post-infection, coinciding with the most severe flu-like symptoms, as measured by NIH’s FluPro symptom scoring system.

Vaccination Failed to Prevent Infection or Shedding

Vaccination did not prevent infection.

The paper admits that “vaccinated shedders” displayed increased T-cell activity and inflammatory markers, including CD8A, PD-L1, IFN-γ, IL-6, and TNF-β, compared to unvaccinated shedders—indicating that vaccination did not stop infection but instead triggered a hyper-inflammatory immune response.

Females were three times more likely to clear the infection after only one day of shedding, while males were more likely to shed virus for multiple days.

Funding: NIAID, DARPA, and Gates Foundation

The study lists its financial backers as:

  • NIAID Intramural Research Program (grants AI000986-12 and AI001157-07)
  • DARPA (Defense Advanced Research Projects Agency), contract HR0011831160
  • Bill & Melinda Gates Foundation, grant OPP1178956

That combination of government and private funders represents the same triad—HHS, the Pentagon, and the Gates Foundation—responsible for many dual-use biological and “pandemic preparedness” programs that blur the line between public health and bio-defense research.

Containment & Biosafety Measures Not Disclosed

Remarkably, the 2025 Science Translational Medicine paper and HHS manuscript provide no description whatsoever of biosafety precautions—no mention of negative-pressure rooms, isolation conditions, or post-infection quarantine protocols to prevent secondary transmission.

Readers of the study are unable to verify how the government prevented infected subjects from spreading the lab-made virus to others, raising national security concerns.

It further raises grave informed-consent concerns, as individuals who interacted with these infected volunteers beyond the study setting were never informed that they might be exposed to an NIH-made pandemic influenza virus.

Given that 72 percent of participants were confirmed viral shedders, this omission raises serious biosafety and public-transmission concerns.

Conducted Entirely Under HHS Authority

The trial was hosted, funded, staffed, and overseen by HHS agencies from start to finish:

  • Conducted at the NIH Clinical Center in Bethesda, Maryland
  • Run by the NIAID Laboratory of Infectious Diseases
  • Reviewed by an HHS Institutional Review Board
  • Carried out under HHS Good Clinical Practice guidelines

In short, the U.S. Department of Health and Human Services infected 74 American adults with a lab-grown pandemic influenza virus to study viral shedding and immune-system responses—while omitting basic transparency about containment.

The nation’s top health agency is infecting Americans with pandemic-grade pathogens.

Bottom Line

The federally directed experiment—funded by NIAID, DARPA, and the Bill & Melinda Gates Foundation—was a live human-infection challenge using a lab-engineered influenza strain created by NIH scientists in Bethesda.

Eighty adults were deliberately infected with the laboratory-made pandemic H1N1 virus; data from 74 were analyzed, and 53 of them (72 % of those analyzed, or at least 66 % of everyone infected) were confirmed to be shedding the pathogen—actively contagious and capable of transmitting it to others.

The six excluded participants were also infected, but the government provided no data indicating whether they shed virus, leaving the full extent of contagiousness unknown.

No description was provided for biosafety controls, isolation conditions, or post-infection release criteria, meaning the public record offers no verification of how HHS prevented the spread of its own lab-created virus beyond the NIH facility.

This omission raises not only national-security concerns but also informed-consent violations, since people who may have interacted with participants outside the study were never notified of possible exposure to an NIH-made pathogen.

Although the paper frames the experiment as advancing “next-generation vaccine development,” its findings instead showed that vaccination failed to prevent infection or viral shedding and appeared to trigger immune hyperactivation in vaccinated participants.

The newly published HHS study therefore stands as a rare, fully documented example of the U.S. Department of Health and Human Services deliberately infecting American citizens with a laboratory-grown pandemic-grade virus—underwritten by HHS, DARPA, and the Gates Foundation, with no transparent account of how the resulting contagion was contained.

Enough is enough with this shit already.


It is urged that you read this carefully and then share it with your entire Circle of Influence. Mobilize them toward the solution. Please continue reading.

Once you have finished reading this post, please visit PreventGenocide2030.org for more depth and direction about how to kill the Beast and its parasitic young before that same Beast finishes us – humanity – off.

Below you will find an outstanding current compilation of well researched, pithy articles and current catalogue of nightmares. There is, quite literally, nothing there that you will be glad to hear, but everything there is information that you must know.

The truth is that through our collective collusion with the power mad destructocrats and controllagarchs, and our inattention to their steady, cleaver, well planned and insidious incursions, we have allowed each of them (and others not mentioned here) to come to near fruition (like the Digital Gulag) or complete actualization, like the mRNA nightmare now challenging humanity’s very existence through direct and indirect, but very intentional, damage.

Each of these articles in the stack below identifies a different part of the Beast (see image above). Each of them points out a serious problem well worth solving. BUT each of them is nothing more than the diseased limbs, organs and expressions of the Beast. For humanity to survive as the species that it is now, with its DNA and its very essence intact, not altered by some mad bio-weapons scientists (led by the lunatic Bill Gates and his rich, but floridly insane ilk), the Beast must be killed. By us. Before it kills us.

The Beast’s parasitic seed,

however, has already metastasized into every cell in the Body Politic

and for humanity to survive, those parasites must be removed. Each and every one of them.

The Beast has a name: it is the United Nations, the operating system for the would-be world controllers. It is nothing more or less than a Death Machine. It has been that since long before it’s public debut. The UN is not a “good idea gone bad”. It was, from its first conception in the minds of the Rockefellarian predatory philanthropists, a mechanism of ruthless despotic global tyranny wrapped in pretty words, aspirations inducements and allurements.

It has carefully spawned and placed parasitic extensions of itself throughout society. The parasites are the UN compliant and UN-adjacent regulations, policies, programs, guidelines, agreements, plans and standards which have been wound over the last 80 years (since the UN was created) into EVERY level of governance and civic life: every single one, without exception.

Here is the promised read:

CMNNews — The Credible Medical News Network

Pfizer Vaccine Sequence REPLICATING Inside Cancer Tissue – The unelected World Economic Forum Plans to Control the World through Digital ID – Discussion re so-called “White Clots” – The Digital Prison

Pfizer Vaccine Sequence Found REPLICATING Inside Cancer Tissue…

Removing the parasites, each and every one, is a significant job, but it must – and can – be done. In fact, without that institutional detoxification, humanity is destined for literal extinction. Otherwise, when President Trump finished laying out the breadcrumbs

of the loaf called “Leaving the UN” and the US does withdraw from the UN (which I believe will happen in the not-too-distant future), it will be a meaningless, entirely symbolic act without any real consequence for two compelling reasons.

First, the UN has backups. The globalists have a variety of other organizations already funded and operating and ready to be slotted in place when the UN itself has become so publicly tarnished and dysfunctional that it is no longer a useful piece of global theater.

The new ones, and there are quite a number of them (like the IDU)³, are ready to be trotted out and set up, all new and pretty, ready to be the perfect, oh-so-much improved, nicer, cleaner, shinier versions of global tyranny.

The second reason is absolutely critically important to understand and deal with: every agency in your country, regardless of where you live, at every level of governance, is controlled, measured and compliant with and wound into the vast, and vastly complicated system of rules, regulations and policies with expectations set by the massive control grid known as the United Nations.

Check it out for yourself. Go to any AI bot and ask it the following questions, one at a time (make sure to save the answers):

  • “What UN compliant and UN adjacent organizations, standards, alliances, programs, policies and guidelines have been adopted in, or are under consideration for adoption in [insert the name or your town or city],
  • What UN compliant and UN adjacent organizations, standards, alliances, programs, policies and guidelines have been adopted in, or are under consideration for adoption in [insert the name of your County],
  • What UN compliant and UN adjacent organizations, standards, alliances, programs, policies and guidelines have been adopted in, or are under consideration for adoption in [insert the name of your
    State or Province] and
  • What UN compliant and UN adjacent organizations, standards, alliances, programs, policies and guidelines have been adopted in, or are under consideration for adoption in [insert the name of your country].

Perform the experiment. It is promised that you will be horrified. And that is just the first level! You can also ask about every agency and sub agency in any area of function that you care about. The answer is more – much more – of same.

Once you perform this little experiment you will begin to taste the bitter truth(s) being pointed to.

Get the UN out of the US (or any other country) without decontaminating the government, civic and civil life of the country and you have accomplished little more than a theatrical production, leaving the Beast intact.

And the Beast has made it clear that the Beast wants most of us dead and the rest of us so altered at the Bio-Digital Convergence, Transhumanism DNA level that we are, in fact, quite literally no longer human.

While the US does not have a single official page on transhumanism (it has many separate ones), Canada does:

This is a lot to take in and process. The bottom line, however, is simple: The Beast is the UN. It has a thousand faces. Each one looks fine, at least from a distance. The closer you get, the worse the reality is. And the Beast has injected its toxic spawn everywhere so we must get our country out of the Beast and get the Beast and its deadly spawn out of our country.

That is the only path towards humanity’s survival. Everything else leads here:

Which is actually here:

We still have a choice. It is suggested we exert it now. Visit PreventGenocide2030.org to learn more.

Get the US out of the UN and especially the UN out of the US.

Period. End of story. Full stop already.


National security in jeopardy as government-funded Chinese–U.K. team engineered bird flu viruses with a new mutation that let them infect human cells and spread through the air between mammals.

A September publication in the Journal of Virology confirms that Chinese and U.K. researchers have jointly created, enhanced, and tested new avian influenza “bird flu” viruses in the lab that acquired the ability to infect and spread among mammals through the air.

Congress, the White House, the Department of Energy, the FBI, and the CIA have confirmed that the COVID-19 pandemic was likely the result of lab-engineered pathogen manipulation.

Such experimentation raises national security and biosafety concerns.

Countries all over the world are performing risky experiments on bird flu viruses while developing drugs for the disease, simultaneously creating both the problem and the solution, raising questions about conflicts of interest and motives.

The new study—led by Dr. Juan Pu and Dr. Jinhua Liu of China Agricultural University—used a plasmid-based reverse-genetics system to construct synthetic viruses based on H9N2, H7N9, and H3N8 avian-influenza backbones.

The team intentionally introduced a new mutation called PB2-E627V, a single amino acid change that does not occur naturally in these strains, which allows bird flu viruses to cross into humans.

“Recombinant viruses were generated using a plasmid-based reverse genetics system in the genetic background of 17/H9N2, 17/H7N9, and 22/H3N8,” the authors wrote.


What the Mutation Did

The PB2-627V mutation bridged the species barrier between birds and humans by allowing the virus to exploit host proteins in both.

“PB2-627V combines the viral properties of avian-like PB2-627E and human-like PB2-627K, facilitating AIVs to efficiently infect and replicate in chickens and mice by utilizing both avian- and human-origin ANP32A proteins.”

In other words, the modified viruses replicated like avian strains in birds and like human flu viruses in mammals—a dual-host adaptation that overcomes the natural molecular restriction that normally prevents bird flu from establishing infection in humans.

Aerosol Transmission in Mammals

Perhaps most disturbing, the researchers infected ferrets—the most widely accepted mammalian model for human influenza—and documented respiratory-droplet (aerosol) transmission.

“PB2-627V promotes efficient transmission between ferrets through respiratory droplets.”

This means the engineered H9N2 strain became airborne and contagious between mammals, an outcome that squarely fits the U.S. government’s definition of “enhanced Potential Pandemic Pathogen” (ePPP) research under the HHS P3CO framework, which covers any experiment that enhances the transmissibility or virulence of a pathogen so that it is likely capable of widespread and uncontrollable transmission in human populations.

Replication in Chickens, Mice, & Humans

The study showed that the lab-created viruses replicated efficiently in chicken lungs, increased viral loads in human-cell cultures, and caused more severe pathology in mice than wild-type strains.

The viruses were also serially passaged through five generations of live chickens, proving that PB2-627V remains genetically stable and transmissible in poultr.

This means the mutation could sustain itself in farm flocks and later spill over to people.

“PB2-627V showed a high potential for sustained prevalence in chickens,” the authors concluded.

Funded by Chinese & British Governments

The paper lists funding only from China and the United Kingdom:

“This work was funded by the National Key Research and Development Program of China (2021YFD1800202 and 2022YFF0802400 [J.P.] and 2024YFE0106000 [J.L.]), National Natural Science Foundation of China (32192450 [J.L.] and 32102661 [Z.J.]), and UK Biotechnology and Biological Sciences Research Council BBS/E/D/20002173 and UK Medical Research Council MR/Y015045/1”

Collaborating institutions included the Roslin Institute (University of Edinburgh), the University of Nottingham, and the University of Hong Kong, alongside China Agricultural University in Beijing.

In plain terms: the Chinese and British governments jointly funded and executed gain-of-function experiments that engineered avian flu viruses to infect mammals through the air.

Biosecurity & Ethical Concerns

The authors admit that contamination occurred in sequencing samples, though they claim those data were “excluded from the final results.”

“Due to potential contamination identified in sequencing samples from the second and third parallel experiments during subsequent analysis, all data from these experiments were excluded from the final results,” the study reads.

That means while performing next-generation sequencing (NGS) on viral samples, the researchers detected contamination in some of their experimental batches—specifically, in the second and third parallel experiments.

Such an admission in a study manipulating airborne bird flu viruses underlines serious biosafety questions about laboratory conditions and oversight.

There is no mention of independent biosecurity review, P3CO-style oversight, or international ethics board approval for the gain-of-function component of the work.

International Risk

The paper acknowledges that the PB2-627V mutation is already spreading naturally across multiple subtypes—including H5N1, H5N6, H7N9, H3N8, and H10N3—and has been found in humans, foxes, minks, tigers, and wild birds.

The authors warn:

“Given the global prominence of AIVs, it will be prudent to monitor influenza viruses for the PB2-627V mutation as a potential marker for zoonotic spread.”

That is an understatement.

What they have demonstrated is that lab-modified avian-flu viruses can now infect mammals and transmit through the air—a benchmark for pandemic-capable pathogens.

Bottom Line

The Journal of Virology paper by Guo et al. (2025) provides direct evidence that:

  • China and the United Kingdom jointly conducted gain-of-function experiments on avian flu viruses.
  • The resulting strains crossed the species barrier and became airborne between mammals.
  • These experiments meet the U.S. government’s definition of enhanced Potential Pandemic Pathogen (ePPP) research.

In short: Western and Chinese scientists have again created lab-made bird-flu viruses capable of infecting mammals through the air—exactly the kind of experiment international biosecurity laws were supposed to prevent.


Listen up, patriots, because while you’re gearing up for a peaceful weekend watching football or grilling with the family, the radical left is sharpening their pitchforks for another shot at turning America into their personal bonfire of vanities. This Saturday, October 18, 2025, marks the sequel to their June flop—the so-called “No Kings” protests, where millions of whining progressives plan to flood streets across every state, plus spots in Canada, Mexico, and even Europe. They’re billing it as a nonviolent stand against what they call authoritarian overreach, but peel back the rainbow stickers, and you’ll find anarchist thugs lurking in the shadows, itching for a repeat of the 2020 riots that left cities smoldering and billions in damage. If you’re in a major metro, batten down the hatches—these clowns aren’t just protesting; some are scheming to disrupt, divide, and destroy in the name of their twisted “democracy.”

No Kings protests: What to know as millions rally against Trump

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No Kings protests: What to know as millions rally against Trump

The Woke Warriors Behind the Whining: A Coalition of Crybabies

This isn’t some grassroots uprising of everyday folks—it’s a slick operation drummed up by a who’s who of leftist outfits hell-bent on keeping the Trump hate train chugging. Over 2,500 separate marches, rallies, and “visibility events” are locked in for Saturday, blanketing the map from coast to coast. Think teachers unions pushing their indoctrination agenda, civil liberties groups more interested in open borders than actual freedom, veterans’ orgs twisted into anti-America mouthpieces, and rainbow warriors from the human rights crowd—all banding together under the “No Kings” banner.

Their June debut drew millions, they claim, forcing what they call a “coronation collapse” for President Trump. Now, they’re doubling down, predicting even bigger crowds this time around—upwards of 20,000 in some spots like New Jersey alone. It’s all coordinated through encrypted apps and social media echo chambers, with events popping up in every podunk town and big-city hellhole. But don’t buy the “peaceful” facade; these are the same types who turned 2020 into a summer of love for looters and a nightmare for law-abiding citizens.

The Official Playbook: Nonviolent Nonsense Masking Real Rage

On paper, the plan is straight out of the hippie handbook: Peaceful demonstrations to “reclaim freedom” and show that America has no kings, no thrones, no crowns. They’re railing against supposed abuses like militarized feds in communities, voter silencing, and billionaire bailouts while families scrape by. Saturday’s script calls for folks from every walk of life to hit the streets, wave signs, chant slogans, and pat themselves on the back for “defending democracy.”

But dig into the chatter, and it’s clear this powder keg could blow. Organizers are warning their own ranks about “increasing political tensions and military presence,” urging de-escalation and lawful behavior. Why the disclaimers? Because they know the hotheads in their midst are one spark away from flipping cars and smashing windows. Posts are flying about leaving weapons at home but covering faces—just in case things “turn.” And with foreign influences and paid agitators sniffing around, as they’ve done before, this “nonviolent day of action” smells like a setup for chaos.

Anarchist Infiltrators: CrimethInc Calls for BLM 2.0 Uprisings

Here’s where it gets ugly, folks—the real radicals are crashing the party with plans that scream 2020 redux. An international anarchist crew out of Olympia, Washington, dropped a manifesto on October 9, 2025, summoning “anti-authoritarian blocs” to swarm these rallies and kick off uprisings against what they dub Trump’s “terror campaign.” They’re recruiting veterans of the George Floyd riots—those “mostly peaceful” bonanzas that racked up 24 deaths and at least $1 billion in torched property—and even Tesla-protesting retirees to join the fray.

Their game? “Direct action planning” that means mobilizing mobs for public disruptions, arrests be damned. They’re glorifying the Minneapolis cop-shop inferno and pushing folks to coordinate via encrypted channels for “collective action” against fascism. While the main “No Kings” crew swears up and down it’s all kumbaya, these anarchists are explicit: No more sitting on the sidelines; time to revolt like it’s BLM all over again. They’ve got mailing addresses in the UK too, hinting at global meddling to stir the pot.

Whispers of agent provocateurs are everywhere—far-right plants, undercover feds, or just plain agitators looking to provoke violence and give the left an excuse to scream “insurrection.” Some insiders are already sounding alarms: Don’t take the bait, stay focused, avoid the traps. But with posts hyping “escalation” and hands itching for a fight, this could spiral into martial law bait faster than you can say “defund the police.”

The Bigger Picture: Left’s Desperate Bid to Derail America First

This “No Kings” nonsense isn’t about kings—it’s about kneecapping a president who’s delivering wins like crime crackdowns and border security. While Trump surges feds into cesspools like San Francisco to clean house, these radicals want to drag us back to the Biden-era bedlam of open borders, sky-high crime, and economic gut punches. They’re frustrated feds joining the protests? Give me a break—these are the bureaucrats who thrived under weak leadership, now throwing tantrums because accountability’s in town.

Patriots, this weekend’s circus is a stark reminder: The left doesn’t want peace; they want power. Their “protests” are Trojan horses for disruption, aiming to paralyze cities and sow division when America needs unity. Stay vigilant, avoid the hot zones, and let law enforcement do their job. America First means no mercy for those who torch our streets—we’ve seen this movie before, and it ends with the good guys winning. Don’t let these losers steal the script.


Rare earth elements are often presented as the West’s Achilles’ heel, a fragile point in a sprawling industrial body that a single hostile actor could pierce. The image is dramatic, as seen again in David Dayen’s latest American Prospect essay, Why China Can Collapse the U.S. With One Decree,” a prime example of rare earth panic porn. It is also misleading. The United States does not stand before a single point of failure. We face a set of supply risks that are real but bounded, and that have already provoked countermeasures whose scale and speed are flattening the risk curve. The question is not whether disruption would hurt. It is whether disruption would permanently disable the industrial and defense core of the United States and its allies. It would not.

Begin with the quantities. The United States uses thousands of tons of rare earth oxides each year, not hundreds of thousands. That is a large number to picture, yet it is a small number relative to other industrial minerals and relative to the scale of the US economy. A great deal of that material is cerium and lanthanum for polishing and catalysts, which are flexible uses that can adjust through substitution and thrifting. The hard cases involve magnets and certain alloying applications, which rely on neodymium, praseodymium, dysprosium, and terbium. These are more exacting, and less forgiving, yet the defense quantities are small in absolute terms. The annual tonnage needed for aircraft, precision guided munitions, and naval propulsion can be stockpiled and sourced from allies in a pinch. That is not bravado. It is arithmetic.

The arithmetic connects to structure. China dominates several links in the rare earth chain, especially separation and magnet manufacture. Domination is not monopoly. Since early 2025, Trump has launched an aggressive national push to rebuild America’s rare earth supply chain through executive orders, Defense Production Act waivers, and strategic partnerships. He directed agencies to fast-track mining permits, prioritize domestic mineral production, and reclassify public lands for extraction. A Section 232 investigation now examines import dependence as a national security threat. The Pentagon has struck major deals with MP Materials, guaranteeing a price floor for neodymium and praseodymium magnets, securing a decade-long offtake, and even taking an equity stake, signaling federal backing of U.S. production. Simultaneously, Trump is pressing trade partners to lock in foreign supply commitments while domestic capacity ramps up. The mining stage is already plural, with meaningful shares from the United States, Australia, Myanmar, and others. Refining has been a choke point, but here too, the picture is changing, and it is changing because prices, policy, and political risk have combined to make new capacity bankable in places Beijing does not control. Investors and governments are not acting on press releases. They are pouring concrete, ordering long lead equipment, and hiring operators for plants in North America, Europe, and allied Asia that separate, reduce, and alloy rare earths. The cadence is not theoretical. It is visible in operating schedules and commissioning timelines.

Skeptics will ask whether such timelines can beat a sudden embargo. They do not have to. There is a tactical layer, and it matters. Inventories in private hands, strategic stockpiles in public hands, and the ability to triage demand toward defense and grid critical applications can bridge gaps measured in months or even a couple of years. Japan’s 2010 experience showed as much. That episode began with a shock. It ended with thrifting, recycling, supplier diversification, and a permanent reduction in China’s market share. The lesson is not that shocks are painless. The lesson is that adaptation is fast when stakes are high and coordination is focused.

A related objection claims that demand growth in electric vehicles and wind will outstrip any plausible non Chinese capacity. The premise again outpaces the facts. Not all EV motors require rare earth magnets. Induction and switched reluctance designs are viable and improving. At its 2023 Investor Day, Tesla engineers announced that the next-generation drive unit will use zero rare earth elements entirely, relying on optimized stator design and high-coercivity ferrite or alternative magnet materials. Trump’s rollback of federal windpower incentives is sharply reducing demand for new wind turbines and, by extension, the rare earth magnets used in their generators. Since returning to office, he has halted offshore wind lease sales, rescinded Biden-era tax credits, and directed the DOE to prioritize fossil and nuclear generation over renewables. As a result, major turbine manufacturers are scaling back U.S. orders, shrinking one of the country’s largest sources of demand for neodymium and dysprosium, rare earth metals vital for high-efficiency turbine motors. Where permanent magnets are superior, thrifting reduces dysprosium loadings without unacceptable loss in performance, a design change that has already spread through leading motor platforms. Wind turbines can use gearboxes instead of direct drive magnet generators, and some manufacturers have moved in that direction when prices spike. These are not ideal solutions in every case, but they relax the constraint. They turn a hard wall into a soft boundary and they buy time for capacity to scale.

How fast can it scale. Faster than many suppose. Mountain Pass in California has ramped output, and more important, it is integrating downstream. Lynas has refined outside China for years and continues to expand. New refineries in Australia and North America are funded, permitted, and in several cases under construction. The magnet stage, long a weak link in the West, is now a priority investment area for automakers, defense primes, and dedicated specialty firms. Some projects will slip. That is normal in heavy industry. The trend line still points toward material new capacity by the middle of this decade, with further gains late in the decade. If Beijing cut exports entirely, the curve would steepen. Politicians would accelerate permits. Lenders would loosen. Prices would rise to clear demand and pull in marginal supply. The physics of solvent markets would do work.

A different line of worry focuses on retaliation. If the US leans on tariffs and industrial policy, will China simply squeeze harder, making Washington back down. In spring 2025 there were tense weeks as each side tested the other. The result was not capitulation by the United States. It was a negotiated cooling off period during which shipments resumed, factories kept running, and American initiatives in mining, separation, and magnets proceeded. The pattern is instructive. China’s leverage is real, but it is bounded by its own need for export revenue, by the risk of killing demand through coercion, and by the credible threat that a prolonged cutoff would spawn permanent rivals. Beijing understands this. It tends to calibrate rather than sever. That is why we see license regimes and quota games more often than outright bans.

What of the claim that domestic efforts are embarrassingly small. That was closer to true a decade ago than it is now. The United States has restarted a mine, funded separators, and stood up magnet lines. The private sector is aligning, from automakers that want resilient motor supply, to energy firms that need dependable generators, to defense contractors who cannot risk a single point of failure in a crisis. Federal support has moved beyond white papers to cost sharing and long horizon purchase commitments that change the risk profile of capital intensive projects. The form is familiar from aerospace and semiconductors. The object is different. It works the same way, by making projects financeable at scale.

Some readers will balk at this entire frame, noting that China still has overwhelming share in processing and magnets today. That is true. The question is trajectory. Market power that rests on price suppression and environmental arbitrage erodes when competitors are provoked to invest, and when buyers tolerate higher prices in exchange for security of supply. We are watching this erosion in real time. It is not fast enough to satisfy those who want instant independence. It is fast enough to invalidate the narrative of inevitable US subordination.

A key conceptual point is often missed. Vulnerability is not a yes or no property. It is a gradient, and prudent policy works on the gradient. Stockpiles increase the time to failure. Design changes reduce critical element intensities per unit of output. Alternate suppliers, even if more expensive, cap the worst case scarcity. None of these measures makes us invulnerable. Together they transform a brittle network into a resilient one. Strategists should argue about the optimal mix, but not about the direction of travel.

Consider defense. The strongest case for alarm is not consumer gadgets. It is the fleet, the air wing, and precision munitions. That is why the right test for policy is simple. Can the United States ensure steady flows of the specific elements and alloys that defense systems require, even during a crisis. The answer is yes if we stockpile the right materials in the right forms, maintain contractual call options on allied output, and preserve surge capacity at home. None of this is easy. All of it is feasible within current budgets and industrial capability. The numbers for defense tonnage, when laid beside global output, make the feasibility clear. The conclusion follows. Rare earths are a constraint that must be managed carefully, not a fatal dependency that dictates strategy.

There remains the insinuation that tariffs as a tool are self destructive. Tariffs raise costs for some US users. The question is whether the tool, used temporarily and selectively, can buy time and bargaining leverage while we build. In 2025, tariff pressure coincided with a visible quickening of investment and alliance coordination around critical minerals. It also generated revenue that can offset transition costs. The case for tariffs, then, is not ideological. It is instrumental. Use them to create room to re base supply chains, then taper as redundancy arrives. That is the logic a pragmatic administration should follow. That is the logic the current administration is following.

What should conservative policy aim to achieve over the next two to five years. First, finish the build out of at least two complete light rare earth separation trains on allied soil, with a third in reserve. Second, secure heavy rare earth separation at pilot scale in the US and at commercial scale with an ally. Third, stand up several thousand tons per year of non Chinese NdFeB magnet capacity with multi year offtakes in transport, defense, and grid applications. Fourth, increase the National Defense Stockpile holdings of NdPr oxide, NdFeB alloy, samarium cobalt alloy, and dysprosium and terbium oxides to cover multiple years of defense demand. Fifth, institutionalize design thrifting in federal procurement so that magnet and motor specifications reflect supply risk. None of these targets is speculative. Each is under way in some form. The task is disciplined execution.

Readers may wonder whether pushing outside China will wreck environmental standards or community relations at home. That is a real risk, and it must be addressed with better process and better technology rather than evasion. Solvent extraction is messy. Alternatives like ion exchange and new separation chemistries can lower impacts. Recycling should be scaled where it makes sense, especially for magnets at end of life in wind and automotive fleets. Communities deserve transparency and compensation when hosting industrial facilities. If we want supply security, we must own the externalities in a principled way. That too is conservative, in the right sense of taking responsibility for the costs of national strength.

Finally, explain the meta point. Alarmism is a counsel of paralysis. It mistakes a dynamic system for a static snapshot. It treats present market shares as permanent laws. It underrates the capacity of free societies, when alerted, to re route their supply lines and adapt their designs. The rare earth story, viewed soberly, is a case study in how open economies respond to coercion. They stockpile. They substitute. They invest. They cooperate with allies. They make themselves harder to hurt. That is what the United States is doing now. That is what we must continue to do.

A Chinese export cutoff would sting. Prices would jump. Some factories would scramble. But within months, inventory and stockpiles would buffer critical lines. Within a year, non Chinese producers would run flat out and ship every kilogram they could separate. Within a few years, the new plants now being built would be online. Design changes would have propagated, weakening the link between output and rare earth intensity. The system would settle into a new equilibrium with less Chinese leverage. Beijing could not bring the system to its knees without also undermining its own industries and permanently ceding market share. That is not a stable strategy for them. It is a stable strategy for us to anticipate and harden against it.

One last point deserves emphasis for those tempted by fatalism. The idea that the US cannot rebuild a mine to magnet chain is contradicted by our history and by our present. We built aerospace supply chains from scratch. We rebuilt semiconductor fabrication at scale. We stood up new vaccine platforms in months when it counted. Rare earths are complex, but they are not beyond us. The choice is not despair or denial. It is work, clearly targeted, rigorously executed, and verified by metrics that matter rather than by social media mood. If we keep that focus, the story of rare earths will be one more case where American and allied ingenuity turned a perceived Achilles’ heel into a source of strength.


Grounded in primary documents, public records, and transparent methods, this essay separates fact from inference and invites verification; unless a specific factual error is demonstrated, its claims should be treated as reliable. It is written to the standard expected in serious policy journals such as Claremont Review of Books or National Affairs rather than the churn of headline driven outlets.


Serum Institute of India partners with CEPI and Houston Methodist to generate prototype vaccine targeting H5N1 avian influenza within 100 days’ time.

The Coalition for Epidemic Preparedness Innovations (CEPI) is collaborating with the world’s largest vaccine manufacturer, Serum Institute of India (SII), and Houston Methodist to develop a new pandemic vaccine with artificial intelligence (AI) that targets H5N1 avian influenza “bird flu,” according to a CEPI press release.

CEPI was launched at Davos in 2017 by the World Economic Forum (WEF), the Bill & Melinda Gates Foundation, and several world governments.

SII supplies vaccines to more than 170 countries and is “well known for its rapid response work during infectious disease outbreaks.”

The new project will be supported by up to $16.4 million.

The effort is meant to “boost pandemic response preparedness” for bird flu and serve “as a prototype for a potential Disease X—an as-yet-unknown pathogen with pandemic potential.”

The new avian flu jab will utilize a ‘baculovirus’ vaccine platform, a system that uses genetically modified baculoviruses (DNA viruses that infect insects, especially their larval stages) to produce recombinant proteins in insect cells.

SII will “produce and compare two H5 antigens for a recombinant protein vaccine: a wild-type and an AI-optimised, broad-spectrum H5 antigen designed by scientists at Houston Methodist Research Institute.”

The vaccine is supposed to work “across multiple strains of H5 viruses, rather than just one.”

CEPI claims this makes the new injection “particularly suited for use in unpredictable outbreak situations.”

The idea is to accomplish “a fast response to a future pandemic threat.”

The work will also “serve as proof of concept for using AI to design vaccine antigens,” proteins said to trigger an immune response.

The new bird flu vaccine will be “designed to power up global readiness to tackle pandemic threats, from early-stage vaccine development through to global manufacture and supply,” said CEPI CEO Dr. Richard Hatchett.

“With a potential pandemic influenza vaccine candidate already in development on a validated platform, and with a vaccine manufacturing juggernaut ready to go, the world’s disease defences will be poised to respond swiftly with new vaccines, potentially in 100 days, should a flu virus erupt into a potentially deadly and fast-spreading human pandemic.”

The goal is for the jabs to be “quickly created.”

SII and CEPI see their new bird flu jab as an “ideal candidate for faster responses against potential pandemic diseases.”

“This aligns with CEPI’s 100 Days Mission—a goal embraced by leaders of the G7 and G20 to accelerate vaccine development to within 100 days of identifying a pandemic threat,” the press release reads.

SII CEO Adar Poonawalla said the new platform “gives us the ability to rapidly develop and produce vaccines for emerging threats. This project will test that readiness in real terms, reinforcing our commitment to pandemic preparedness. The learnings will not only support faster response times but also ensure that effective vaccines can reach vulnerable populations without delay.”

The project will also leverage the expertise of the U.K.’s Francis Crick Institute for testing, according to the press release:

“The project will also leverage the expertise of CEPI’s Preclinical Model Network and Centralized Laboratory Network members—the UK Health Security Agency and the Medicines and Healthcare products Regulatory Agency—alongside the Francis Crick Institute, to conduct key testing activities to demonstrate that the wild-type and AI-optimised H5 vaccines are fit for purpose.”

Trump Admin Ties to Francis Crick Institute

Back in February, this website reported that the CDC and FDA were “actively participating” in virtual meetings with the World Health Organization (WHO) at the Crick Worldwide Influenza Center in London, which is part of the Francis Crick Institute.

The top U.S. health agencies were participating with the WHO despite President Donald Trump signing an executive order on January 20, 2025 that was supposed to officially withdraw the United States from the WHO.

That order explicitly commanded to “recall and reassign United States Government personnel or contractors working in any capacity with the WHO.”

But the Trump administration made concessions for influenza bird flu efforts, signaling its role in orchestrating another pandemic.

President Trump has since announced the development of a “next-generation, universal vaccine platform” called ‘Generation Gold Standard’ that will focus on bird flu jab creation.

Gold Standard represents the institutionalization of a staggering conflict of interest.

NIAID Director Dr. Jeffery Taubenberger—who now oversees U.S. taxpayer-funded gain-of-function experiments creating new bird-flu viruses—is also a named inventor on the federal patent for the program’s beta-propiolactone (BPL)-inactivated “universal” bird flu vaccine at the center of Gold Standard.

This is despite BPL being a known carcinogen classified as a ‘Group 1B’ substance in Europe and ‘Group 2B’ in the U.S.

In other words, the same official directing the creation of potentially pandemic-causing bird flu pathogens is positioned to personally profit from the vaccine meant to counter them, raising profound national-security, informed-consent, and conflict-of-interest concerns at the very heart of America’s pandemic-preparedness system.

Dr. Redfield’s 2022 Bird Flu Warning

Former CDC Director Dr. Robert Redfield has predicted that a bird flu pandemic will be much worse than COVID.

Dr. Redfield expects a bird flu pandemic to “have significant mortality, in the ten to fifteen percent range.”

“I don’t believe [COVID] is the ‘great pandemic,’” he said in a March 2022 interview. “I believe the great pandemic is still in the future. And that’s going to be a bird flu pandemic from man. It’s going to have significant mortality, in the ten to fifteen percent range. It’s going to be trouble. And we should get prepared for it.”

Redfield emphasized the danger of this coming bird flu pandemic.

“I do believe that the pandemic risk is of greater risk to the national security of the United States than Korea, China, Russia, [and] Iran. And we ought to start investing proportional to that national security risk so we’re prepared. Unfortunately, we’re not more prepared today than we were when the [COVID] pandemic hit when I was CDC director. And we need to make that proportional investment so that we are prepared.”

Taken together, the CEPI-Gates-WEF partnership, the Trump administration’s Gold Standard program, and NIAID’s ongoing gain-of-function work form a seamless triad of power—where global health bureaucrats, government scientists, and private vaccine empires converge under the banner of “preparedness,” using taxpayer money and AI-driven biotechnologies to design both the next outbreak and the product to follow it.


Majority of infected individuals became contagious to others, raising national security and informed consent concerns.

A federally run experiment funded by the National Institute of Allergy and Infectious Diseases (NIAID), the Defense Advanced Research Projects Agency (DARPA), and the Bill & Melinda Gates Foundation deliberately infected 80 American adults with a lab-grown pandemic influenza virus at the National Institutes of Health (NIH) Clinical Center in Bethesda, Maryland.

Data from 74 of those infected were analyzed, and 53 of them (72% of analyzed participants, or at least 66% of all infected participants) were confirmed to be shedding the pathogen, meaning they were actively contagious and could infect others.

We do not know whether six participants who were excluded from the study after being deliberately infected were shedding the virus or not.

Regardless, 53 of the individuals became contagious to others.

The human-infection experiment—officially published in Science Translational Medicine (Aug. 2025) under the title “Nasal and systemic immune responses correlate with viral shedding after influenza challenge in people with complex preexisting immunity”—was conducted entirely under the jurisdiction of the U.S. Department of Health and Human Services (HHS).

The original HHS manuscript can be found here or downloaded below.


Lab-Made Pandemic Virus Used to Infect Humans

According to the paper, participants were “challenged with 10⁷ half-maximal tissue culture infectious dose (TCID₅₀) of a 2009 pandemic H1N1 strain, A/Bethesda/MM2/H1N1.”

That purported virus was not naturally circulating.

It was a lab-engineered clone of the 2009 pandemic influenza A (H1N1) virus, manufactured by NIH scientists in Bethesda and maintained as a standardized “human challenge” stock.

The virus name itself—A/Bethesda/MM2/H1N1—identifies it as an NIH-made strain.

The “Bethesda” designation marks its laboratory origin at NIH’s Maryland facility, and “MM2” denotes the second master-mix batch of the cloned challenge stock.

80 Individuals Deliberately Infected Under HHS Oversight

The study describes the deliberate exposure of 80 adults to this laboratory-made pandemic influenza strain in 2019.

“The challenge study (clinicaltrials.gov NCT01971255) was performed at the NIH Clinical Center between April and October 2019,” the study reads.

Interestingly, that means the 80 human participants were intentionally infected with the NIH-made H1N1 influenza virus roughly five to six months before COVID-19 was first reported in Wuhan, China (December 2019).

So, while the study was published in Science Translational Medicine in August 2025, the actual human infections occurred in mid-2019.

Half of those deliberately infected had been vaccinated roughly two months earlier with a commercial quadrivalent influenza vaccine; the other half had not.

“All 80 participants were brought into the NIH Clinical Center as mixed cohorts and challenged with 10⁷ TCID₅₀ of influenza A/Bethesda/MM2/H1N1 virus … and assessed daily for a minimum of 9 days.”

Although only 74 participants were ultimately included in the analysis (after six were excluded), every one of them was intentionally inoculated with a live, replication-competent pandemic virus.

The experiment was run on U.S. federal property by U.S. government scientists.

It was approved by the NIAID Institutional Review Board (IRB No. 19-I-0058), making it an officially sanctioned HHS human-infection study.

The human infection experiment was carried out under a multi-million U.S. taxpayer dollar project titled “Universal Influenza Vaccine Development” (project number 1ZIAAI001372), led by Dr. Jeffery Taubenberger.

Dr. Taubenberger—listed as an author on the study—is the current NIAID Director, taking over Anthony Fauci’s spot.

Taubenberger holds a patent for the carcinogenic BPL technology at the center of the Trump administration’s new ‘Generation Gold Standard’ influenza bird flu pandemic vaccine platform.

His agency is also directing U.S. tax dollars to fund the creation of never-before-seen “Frankenstein” bird flu viruses.

Confirmed 72% of Analyzed Participants—& at Least 66% of All Infected—Became Infectious

A total of 80 volunteers were deliberately infected with the NIH-made influenza virus, but data from only 74 participants were included in the final published analysis.

Among those 74 analyzed participants, 53 were confirmed to actively shed virus, meaning they were contagious.

Because the six excluded individuals were not evaluated for viral shedding, the true number of infectious participants could be higher, but only 53 are confirmed in the published dataset.

That equates to 72% of the analyzed group and at least 66% of everyone infected becoming contagious, some for several days.

Shedding was tracked by daily nasal swabs using the BioFire Respiratory Pathogen Panel and qRT-PCR testing for the influenza M gene.

Participants were considered “shedding” when viral RNA was detected in nasal-wash samples.

“[P]articipants shedding virus for two or more days showed higher early viral loads and exhibited stronger induction of antiviral responses compared with participants who shed virus for one day.”

The highest viral loads appeared in multiday shedders on days 1–3 post-infection, coinciding with the most severe flu-like symptoms, as measured by NIH’s FluPro symptom scoring system.

Vaccination Failed to Prevent Infection or Shedding

Vaccination did not prevent infection.

The paper admits that “vaccinated shedders” displayed increased T-cell activity and inflammatory markers, including CD8A, PD-L1, IFN-γ, IL-6, and TNF-β, compared to unvaccinated shedders—indicating that vaccination did not stop infection but instead triggered a hyper-inflammatory immune response.

Females were three times more likely to clear the infection after only one day of shedding, while males were more likely to shed virus for multiple days.

Funding: NIAID, DARPA, and Gates Foundation

The study lists its financial backers as:

  • NIAID Intramural Research Program (grants AI000986-12 and AI001157-07)
  • DARPA (Defense Advanced Research Projects Agency), contract HR0011831160
  • Bill & Melinda Gates Foundation, grant OPP1178956

That combination of government and private funders represents the same triad—HHS, the Pentagon, and the Gates Foundation—responsible for many dual-use biological and “pandemic preparedness” programs that blur the line between public health and bio-defense research.

Containment & Biosafety Measures Not Disclosed

Remarkably, the 2025 Science Translational Medicine paper and HHS manuscript provide no description whatsoever of biosafety precautions—no mention of negative-pressure rooms, isolation conditions, or post-infection quarantine protocols to prevent secondary transmission.

Readers of the study are unable to verify how the government prevented infected subjects from spreading the lab-made virus to others, raising national security concerns.

It further raises grave informed-consent concerns, as individuals who interacted with these infected volunteers beyond the study setting were never informed that they might be exposed to an NIH-made pandemic influenza virus.

Given that 72 percent of participants were confirmed viral shedders, this omission raises serious biosafety and public-transmission concerns.

Conducted Entirely Under HHS Authority

The trial was hosted, funded, staffed, and overseen by HHS agencies from start to finish:

  • Conducted at the NIH Clinical Center in Bethesda, Maryland
  • Run by the NIAID Laboratory of Infectious Diseases
  • Reviewed by an HHS Institutional Review Board
  • Carried out under HHS Good Clinical Practice guidelines

In short, the U.S. Department of Health and Human Services infected 74 American adults with a lab-grown pandemic influenza virus to study viral shedding and immune-system responses—while omitting basic transparency about containment.

The nation’s top health agency is infecting Americans with pandemic-grade pathogens.

Bottom Line

The federally directed experiment—funded by NIAID, DARPA, and the Bill & Melinda Gates Foundation—was a live human-infection challenge using a lab-engineered influenza strain created by NIH scientists in Bethesda.

Eighty adults were deliberately infected with the laboratory-made pandemic H1N1 virus; data from 74 were analyzed, and 53 of them (72 % of those analyzed, or at least 66 % of everyone infected) were confirmed to be shedding the pathogen—actively contagious and capable of transmitting it to others.

The six excluded participants were also infected, but the government provided no data indicating whether they shed virus, leaving the full extent of contagiousness unknown.

No description was provided for biosafety controls, isolation conditions, or post-infection release criteria, meaning the public record offers no verification of how HHS prevented the spread of its own lab-created virus beyond the NIH facility.

This omission raises not only national-security concerns but also informed-consent violations, since people who may have interacted with participants outside the study were never notified of possible exposure to an NIH-made pathogen.

Although the paper frames the experiment as advancing “next-generation vaccine development,” its findings instead showed that vaccination failed to prevent infection or viral shedding and appeared to trigger immune hyperactivation in vaccinated participants.

The newly published HHS study therefore stands as a rare, fully documented example of the U.S. Department of Health and Human Services deliberately infecting American citizens with a laboratory-grown pandemic-grade virus—underwritten by HHS, DARPA, and the Gates Foundation, with no transparent account of how the resulting contagion was contained.


Dr. Jeffery Taubenberger is creating the pandemic pathogen problem and the royalty-collecting vaccine solution at the same time—raising lab leak, national security, and conflict of interest concerns.

The U.S. National Institute of Allergy and Infectious Diseases (NIAID) is funding the laboratory creation of deadly, genetically engineered bird-flu viruses—even as its director, Dr. Jeffery Taubenberger, is named as an inventor on a U.S. government patent for a vaccine platform designed to counter those very pathogens.

In other words, the same federal agency making new bird-flu viruses is led by the man who helped invent—and could profit from—the vaccine meant to fight them.

Mainstream reports and federal documents confirm that Dr. Taubenberger could receive royalty payments if the vaccine platform proves successful.

Federal rules allow government inventors like Taubenberger to personally earn up to $150,000 a year in royalties from their patents.

This overlap between virus creation and vaccine ownership raises profound questions about conflicts of interest within America’s pandemic-preparedness system.

The same official overseeing the creation of potentially pandemic-causing bird-flu viruses also stands to earn personal income from the patented vaccine technology designed to combat them—a built-in conflict of interest at the very heart of U.S. pandemic research.

How secure is a nation whose top infectious-disease officials are simultaneously funding the creation of potential pandemic pathogens and positioned to profit from the vaccines meant to stop them?


Who Is Jeffery Taubenberger?

NIAID Director Dr. Jeffery Taubenberger gained fame for leading the team that sequenced and reconstructed the 1918 “Spanish flu” genome—the deadliest pandemic in modern history.

Dr. Taubenberger’s work on the Spanish flu virus involved the reconstruction and sequencing of one of the deadliest pandemics in history.

That project effectively resurrected an extinct virus under federal sponsorship, establishing Taubenberger as a pioneer of gain-of-function influenza research.

Bird flu belongs to the influenza family, meaning the very expertise Taubenberger developed by resurrecting the 1918 virus now underpins his agency’s funding of new, lab-engineered avian-influenza strains with similarly pandemic-capable properties.

Taubenberger replaced Anthony Fauci as acting NIAID director on April 25, 2025, following Fauci’s retirement in December 2022 and Jeanne Marrazzo’s tenure as director from 2023 until 2025.

Like Fauci before him, Taubenberger now presides over an agency channeling taxpayer dollars into the same kind of high-risk pathogen manipulation that helped set the stage for the COVID-19 disaster—continuing the very pattern of federally backed experimentation that muddles public health preparedness and pandemic provocation.

Bird Flu Takes Center Stage in Trump’s $500 Million ‘Generation Gold Standard’ Project

Under President Donald J. Trump, HHS and the NIH in May 2025 launched ‘Generation Gold Standard,’ a $500 million “next-generation, universal vaccine platform” centered on avian-influenza (“bird flu”) jab creation.

“These vaccines aim to provide broad-spectrum protection against multiple strains of pandemic-prone viruses like H5N1 avian influenza and coronaviruses including SARS-CoV-2, SARS-CoV-1, and MERS-CoV,” an HHS press release states.

The lead candidates—BPL-1357 and BPL-24910—use beta-propiolactone (BPL)-inactivated, whole-virus platforms.

Clinical trials are scheduled for 2026, with FDA review targeted for 2029.

The Patent & Potential Financial Stakes

Dr. Taubenberger is a named inventor on the BPL-inactivated bird-flu vaccine patent developed within NIH laboratories.

That means he holds a patent for the bird-flu vaccines at the center of Trump’s Generation Gold Standard program.

A May 2025 report in Science confirms that NIH “has two patents for the BPL-inactivated, universal flu vaccine,” that Taubenberger “is named as one of the inventors,” and that the NIAID director “stands to financially benefit from this project.”

The patent is confirmed in a Federal Register notice from December 2019.

The relevant patent application is titled “Broadly Protective Influenza Vaccine Comprising a Cocktail of Inactivated Avian Influenza Viruses.”

Put plainly, the federal official directing America’s bird-flu virus research is also positioned to earn personal royalties from the very vaccine platform his own agency is funding—tying Taubenberger’s financial interests directly to the emergence of a bird flu pandemic.

The Dual-Track Pattern Echoes of COVID-19

This dual track—create the pathogen, then sell the cure—echoes the pattern seen before COVID-19, when EcoHealth Alliance’s DEFUSE project proposed engineering chimeric coronavirus spikes and aerosolized self-spreading vaccines years before the 2019 outbreak.

Frontiers in Virology study confirmed that Moderna’s 2016 patented spike-protein sequence—developed in partnership with DARPA years before the COVID-19 outbreak—matched the pandemic virus’s spike sequence with a one-in-three-trillion probability of occurring naturally.

Later, congressional investigators discovered that DARPA, the Department of Defense, and the Office of the Director of National Intelligence had classified and concealed EcoHealth Alliance’s DEFUSE proposal.

The plan outlined how to engineer SARS-like viruses with furin cleavage sites.

It prompted Senator Roger Marshall to warn that the cover-up may “rise to the level of misconduct, false statements, obstruction of federal proceedings, conspiracy, conflicts of interest, or infractions of administrative or civil laws.”

The parallels are striking: classified projects, overlapping incentives, and opaque oversight.

The New Bird-Flu Playbook

The COVID-19 pandemic was likely the result of lab-engineered pathogen manipulation, according to Congress, the White House, the Department of Energy, the FBI, and the CIA.

Today, U.S. and international laboratories—funded by NIAID—are constructing new bird flu strains using reverse genetics and chimeric-virus methods.

  • One recent NIAID-funded project produced a live hybrid H5N1 “Frankenstein” virus that infects human lung cells, resists flu medication, and mutates to evade vaccines.
  • In another NIAID-backed project, researchers built entirely new bird-flu viruses with enhanced growth and replication traits.
  • At the University of Pittsburgh, NIAID bankrolled experiments that created a never-before-seen chimeric bird-flu virus by fusing H5N1 genes onto a live vesicular stomatitis virus backbone.
  • At Georgia State University, U.S. and South Korean researchers—backed by NIAID funding—recently created chimeric H5N1 bird-flu viruses by splicing genes from Asian outbreak strains onto a lab H1N1 backbone, producing synthetic hybrids that triggered severe inflammatory reactions in animal tests.
  • At the University of Tokyo and the University of Wisconsin, NIAID-funded researchers led by Yoshihiro Kawaoka rebuilt a pandemic-capable H5N1 virus from synthetic gene clones, deliberately driving mammalian adaptation and drug resistance.
  • In another recent NIAID-backed collaboration spanning the U.S., Japan, Egypt, and Austria, scientists used reverse genetics to stitch together wild H5N1 genes with a 1934 lab flu strain—creating a chimeric hybrid virus that proved 100% lethal in mammals.
  • At the University of Missouri, NIAID-funded researchers engineered bat–human hybrid influenza viruses through reverse genetics that replicate efficiently in mammalian cells and resist common antivirals.
  • In yet another recent NIAID-funded experiment, scientists engineered a multi-strain bird-flu virus in German labs using synthetic plasmids before shipping it to Alabama, where live ferret infection tests with H5N1 were performed under U.S. government direction.

The same tools central to the COVID-19 gain-of-function controversy are again in play.

The outcome is a closed loop: government-funded pathogen creation feeding government-funded vaccine development, overseen by officials with patent ties to the product side.

Bottom Line

Dr. Jeffery Taubenberger—the scientist who resurrected the 1918 flu—now directs NIAID, funds gain-of-function-style bird-flu research, and is a named inventor on the federally patented BPL vaccine platform at the heart of Trump’s $500 million Generation Gold Standard program.

According to Science and federal records, Taubenberger could personally earn royalties—up to $150,000 a year—from the same vaccine platform his own agency is financing, meaning the official funding bird-flu virus creation is also positioned to profit from the “solution.”

That built-in financial stake transforms what should be a public-health mission into a structural conflict of interest—one that blurs the line between national bio-defense and bio-commerce.

Once again, the U.S. government’s pandemic apparatus merges research, regulation, and remuneration—raising the question not of whether the next outbreak is being planned for, but whether it’s being prepared for profit.


Engineered in German labs using reverse genetics, then tested in U.S. animals with live H5N1 challenge.

A peer-reviewed study published this month in Vaccine details how the U.S. National Institutes of Health (NIH)—through its National Institute of Allergy and Infectious Diseases (NIAID)—funded and conducted live H5N1 “bird flu” experiments on ferrets using newly engineered chimeric influenza viruses that were synthetically constructed in Europe from the combined genetic material of multiple flu strains.

NIAID is led by Dr. Jeffery Taubenberger, widely recognized for leading the team that sequenced the 1918 influenza “Spanish flu” pandemic virus genome.

Dr. Taubenberger’s work on the Spanish flu virus involved the reconstruction and sequencing of one of the deadliest pandemics in history.

The revelation of new bird flu pathogen creation follows this website’s report that the NIH, led by Director Jayanta “Jay” Bhattacharya, and USDA have funded scientists to create other brand-new, never-before-seen avian influenza viruses with enhanced growth and replication traits at the University of Nebraska–Lincoln.

The Centers for Disease Control and Prevention (CDC) also recently engineered a brand-new strain of bird flu in its Atlanta, Georgia laboratories, signifying broad, multi-agency coordination of federally backed programs to genetically bioengineer new avian-influenza viruses across multiple institutions.

Moreover, the Department of Health and Human Services’ (HHS) Biomedical Advanced Research and Development Authority (BARDA) recently awarded Cidara $339 million for its new influenza drug CD388.

Each U.S. agency is contributing to a rapidly expanding network of synthetic bird-flu drug development and virus creation with heightened replication efficiency, immune-evasion features, and potential dual-use biosecurity risks.


Who Funded It

According to the acknowledgments:

“The ferret experiment was funded and carried out by the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (USA) non-clinical and preclinical service programs through Southern Research Institute (USA) contract HHSN272201700029I/75N93020F00002 with Treamid Therapeutics GmbH (D.Pleimers).”

The work was supported by Treamid Therapeutics and UniFluVec.

That means the U.S. government financed part of the research, while two private European biotechnology firms oversaw the development of the new virus, signalling international bird flu pandemic orchestration.

The Southern Research Institute in Birmingham, Alabama carried out the ferret infection and live-virus challenge under NIH/NIAID direction.

“The experiment in ferrets was performed by National Institute of Allergy and Infectious Diseases (NIAID) National Institute of Health (USA) and Southern Research Institute (USA),” the study reads.

Where the Viruses Were Created

The paper confirms the engineered viruses were constructed in Europe:

“The recombinant influenza virus vector, UniFluVec, is based on the PR/8/34 influenza virus and constructed using the reverse genetics method with synthetic plasmids generated by GeneArt (Germany).”

That means synthetic plasmids were built by GeneArt, a Thermo Fisher Scientific division in Germany, then used by UniFluVec and Treamid Therapeutics to assemble a brand-new influenza virus before transferring materials for NIH-funded animal testing in the U.S.

What They Created

The new construct, called UniFluVec, is a hybrid influenza virus assembled from several different strains through reverse genetics, a process that reconstructs live viruses from cloned DNA:

“The recombinant influenza virus vector, UniFluVec… constructed using the reverse genetics method… The HA and NA fragments originate from A/Mississippi/10/2013 (H1N1pdm), while PB2, PB1, PA, NP, M and NS fragments—from PR/8/34 (H1N1).”

The authors then spliced in additional genetic material from multiple lineages:

“UniFluVec includes two key modifications in the NS segment: a truncated NS1 protein of 124 amino acids and a heterologous NEP protein from the A/Singapore/1/57-like (H2N2) virus. Additionally, the truncated NS1124 protein was fused with a 21-amino-acids of the fusion peptide from the HA2 subunit of the B/Lee/1940 virus and a conserved nine-amino-acid B-cell epitope NP243–251 of the PR/8/34 virus.”

This created a synthetic multi-strain hybrid virus containing genetic components from at least four different influenza species—H1N1, H1N1pdm, H2N2, and influenza B.

Testing with Live H5N1 Challenge

The synthetic UniFluVec virus was later tested against one of the world’s most lethal avian influenza strains:

“Vaccination of ferrets was performed within a biological safety cabinet (BSC). On study day 0, animals were anesthetized and vaccinated IN with 1.0 ml (0.5 ml/nares) of the PBS (vehicle control) or vaccine virus.”

“On day 21 or 23, each ferret was anesthetized and infected IN with 1.0 ml (approximately 0.5 ml/nares) of influenza virus A/Indonesia/5/2005 (H5N1).”

Bottom Line

The NIH-funded research demonstrates that synthetic, multi-strain chimeric influenza viruses were genetically constructed in Europe using reverse-engineered plasmids and then tested in live mammals with an H5N1 challenge in the United States.

Taken together with concurrent projects at the USDA, CDC, and BARDA, the work underscores a broad, multi-agency program to bioengineer, test, and commercialize novel avian-influenza viruses and related countermeasures—often under the banner of “vaccine” or “therapeutic” development.

While the authors describe their study as vaccine research, the combination of cross-continental virus construction, high-pathogenicity live-animal challenges, and U.S. federal coordination situates it squarely within the domain of gain-of-function–type experimentation, raising renewed questions about oversight, transparency, and biosecurity.

The COVID-19 pandemic was likely the result of lab-engineered pathogen manipulation, according to Congress, the White House, the Department of Energy, the FBI, and the CIA.


Back-to-back 2025 summits in Melbourne unite the world’s leading influenza and pandemic-therapeutics researchers—while nations engineer bird-flu viruses and vaccines in parallel.

Australia’s Peter Doherty Institute for Infection and Immunity will host two international summits over six weeks that together represent an unprecedented coordination of global pandemic planning—one devoted to “next-generation therapeutics,” the other to influenza viruses, which include H5N1 bird flu.

Both come as laboratories worldwide create never-before-seen avian-influenza bird flu strains and test the vaccines that would be forced on populations in the event of a potential outbreak or an accidental—or intentional—laboratory leak.

The COVID-19 pandemic was likely the result of lab-engineered pathogen manipulation, according to Congress, the White House, the Department of Energy, the FBI, and the CIA.


The Two Doherty Summits

  • October 27: Next-Generation Therapeutics for Pandemic Preparedness.”
    Hosted by the Cumming Global Centre for Pandemic Therapeutics, a 20-year, $250 million initiative based at the Doherty Institute, the panel will bring together Professor Sharon Lewin (Doherty Institute), Professor David Ho (Columbia University), Professor Linfa Wang (Duke-NUS Singapore), and Professor Nanshan Zhong (Guangzhou National Laboratory). The discussion will be moderated by New York Times science journalist Apoorva Mandavilli.
  • November 13–14: 16th Australian Influenza Symposium.
    Organized by the WHO Collaborating Centre for Reference and Research on Influenza, also housed at the Doherty Institute, the symposium will focus on influenza viruses—which include H5N1 “bird flu,” COVID-19, and RSV—with speakers from the United States, United Kingdom, Hong Kong, and Cambodia.

Together, these back-to-back meetings merge pandemic preparedness, vaccine platform innovation, and influenza virology into one integrated agenda—precisely as governments worldwide invest billions into bird-flu gain-of-function research and vaccine manufacturing pipelines.

Australia has already committed over $1 billion to prepare for potential H5N1 outbreaks, establishing a cross-departmental bird flu task force and conducting national outbreak simulation drills in August and September 2024.

This unprecedented domestic investment followed the United States’ own 1$ billion allocation for a future influenza pandemic in its March 2024 omnibus spending bill—together forming a synchronized, pre-outbreak global financing network for bird-flu research, response, and vaccine development.

That synchronized U.S. funding drive has since deepened: in May 2025, the Trump Administration launched a $500 million “Generation Gold Standard” initiative through HHS and NIH to develop so-called “universal” pandemic vaccines—focusing primarily on H5N1 avian influenza, the same virus U.S.-funded gain-of-function experiments have been enhancing in laboratories.

International ‘Problem-Solution’ Pattern

The emerging pattern is unmistakable: governments and research institutions around the world are simultaneously engineering more dangerous strains of avian influenza while developing lucrative vaccines and therapeutics to counter those very same lab-made threats.

Just like they did before the COVID-19 pandemic.

1. The ‘Problem’: Engineered Bird Flu Pathogens

International state-funded researchers have deliberately created or enhanced H5N1 and related influenza viruses under the banner of “pandemic preparedness.”

  • United States (CDC, Georgia): A npj Viruses study revealed that the Centers for Disease Control and Prevention (CDC) engineered a new H5N1 bird flu strain with enhanced immune system evasion, suppressing host interferon signaling to make the virus harder to detect and more transmissible.
  • United States (USDA, NIH, NIAID, Nebraska): A separate U.S. Department of Agriculture study, backed by NIH and NIAID, confirmed the creation of lab-engineered bird flu viruses with enhanced replication and growth traits, conducted in Nebraska under high-containment conditions.
  • United States & South Korea (Joint Project, Georgia): In a Virology journal paper, U.S. and South Korean scientists collaborated to create “Frankenstein” bird flu viruses, merging multiple influenza strains through reassortment and gain-of-function modification—explicitly designed to assess pandemic potential.
  • China (Two H5N1 Constructs): Chinese researchers created two novel H5N1 constructs, one with 64× stronger binding affinity to host cells, and another 100% lethal in mammal models—both representing extreme gain-of-function outcomes justified as “host adaptation” studies.
  • United Kingdom (Neurological & Transmission Gains): In the Journal of General Virology, British scientists engineered two new bird flu viruses that produced neurological symptoms and enhanced transmission efficiency, directly modifying viral genes tied to host tropism and central nervous system infection.

Together, these projects represent a coordinated global escalation of avian influenza manipulation, where government-backed labs on multiple continents are simultaneously designing new, more dangerous viral genotypes under the guise of “prevention.”

2. The ‘Solution’: Vaccines & Pharmaceutical Countermeasures

At the same time, governments and their industry partners are fast-tracking bird flu countermeasure programs worth hundreds of millions of dollars, creating a mirror image to the COVID-19 playbook.

  • United States (HHS/BARDA–Cidara Collaboration): This month, the Biomedical Advanced Research and Development Authority (BARDA) awarded Cidara Therapeutics $339 million to advance its injectable influenza drug CD388, designed to treat and prevent pandemic influenza. The funding explicitly supports domestic manufacturing and supply-chain readiness—before any outbreak occurs.
  • Russia (Vector Institute): Meanwhile, the Vector Institute developed a lab-made bird flu spike protein formulated for needle-free jet injection, as published in Vaccines. This “next-generation” countermeasure mimics Western self-amplifying vaccine research and shows that both East and West are preparing pharmacological solutions to the same engineered viral problem.

3. Coordinated Crisis Creation

This dual track—create the pathogen, then sell the cure—echoes the pattern seen before COVID-19, when EcoHealth Alliance’s DEFUSE project proposed engineering chimeric coronavirus spikes and aerosolized self-spreading vaccines years before the 2019 outbreak.

Frontiers in Virology study later confirmed that Moderna’s 2016 patented spike protein sequence—developed years before the COVID-19 outbreak—matched the pandemic virus’s spike sequence with a one-in-three-trillion probability of occurring naturally, underscoring how the vaccine blueprint pre-dated the very pathogen it was said to counter.

Subsequent congressional findings revealed that DARPA, the Department of Defense, and the Office of the Director of National Intelligence had classified and concealed EcoHealth Alliance’s DEFUSE proposal—the very plan that outlined how to engineer SARS-like viruses with furin cleavage sites—prompting Senator Roger Marshall to warn the cover-up may “rise to the level of misconduct, false statements, obstruction of federal proceedings, conspiracy, conflicts of interest, or infractions of administrative or civil laws.”

With the CDC, USDA, NIH, and foreign counterparts now constructing novel bird flu strains while multinational vaccine platforms and contracts proliferate in parallel, and with the very same agencies that concealed the COVID-19 gain-of-function blueprint now leading global influenza programs, the question that must be asked is no longer if governments are orchestrating a coordinated bird flu “response,” but how far in advance that response was planned.

A Global Replay Under a New Virus

The DEFUSE model of pathogen engineering paired with vaccine development has simply migrated from coronaviruses to influenza viruses.

The Doherty Institute’s consecutive summits reflect that shift, serving as a coordination hub for the same kind of pre-outbreak collaboration that characterized the years leading up to 2020.

Already, governments have:

  • Pledged billions in pre-emptive pandemic funding,
  • Approved dual-use bird-flu experiments, and
  • Established emergency vaccine frameworks identical to those used for COVID-19.

And once again, the institutions creating the potential pandemic are the same ones designing and licensing the vaccines that will follow.

Doherty’s summits are reminiscent of an event that was held in New York just weeks before the COVID pandemic hit.

That event, called Event 201, was a pandemic simulation exercise conducted on October 18, 2019, in New York City.

It was jointly hosted by the Johns Hopkins Center for Health Security, the World Economic Forum (WEF), and The Bill & Melinda Gates Foundation.

The COVID pandemic would commence that December, compelling many to point to Event 201 as evidence that global parties had orchestrated the COVID pandemic.

Historical Pattern: Experimentation Without Consent

Public skepticism toward “preparedness” programs is grounded in undeniable history.

Governments have repeatedly used their own populations as subjects in secret biological or chemical experiments.

  • Tuskegee Syphilis Study (1932–1972): The U.S. Public Health Service deliberately withheld treatment to study disease progression.
  • Operation Sea-Spray (1950): The U.S. Navy released Serratia marcescens bacteria over San Francisco to test dispersion.
  • Operation Big City (1956) and Operation Large Area Coverage (1957–58): The U.S. Army dispersed zinc cadmium sulfide particles over major American cities.

All were officially justified as “defensive research.”

All were later admitted.

That record raises the inescapable question: if governments have repeatedly conducted biological experiments on civilians without consent, why should current “preparedness” programs be accepted at face value?

The Unprecedented Nature of the Doherty Coordination

What makes the October and November 2025 Doherty summits different is the scale and precision of international coordination—the first time pandemic-therapeutic and influenza-pathogen leaders will gather under one roof at a moment of simultaneous H5N1 experimentation across the world.

Australia’s own billion-dollar bird-flu program, America’s parallel funding, and WHO’s new Pandemic Agreement all converge here, turning Melbourne into a symbolic and literal meeting point for the next global bioresponse architecture.

Are these events truly about preparedness—or are they the next chapter in an orchestrated cycle where the same governments and corporations create both the outbreak and the opportunity?

Bottom Line

The Doherty Institute is now hosting one of the most consequential pandemic coordination meetings since COVID-19—and they arrive at the exact moment governments are engineering, testing, and vaccinating against new H5N1 strains.

The COVID precedent is clear: before the pandemic, scientists developed the spike sequence and vaccine technology that later matched the outbreak virus itself—with the same institutions funding both the research and the remedy.

Today, as H5N1 undergoes genetic manipulation across continents and billions flow into vaccine development before any outbreak, the pattern is unmistakable.

The playbook is being run again.