Health Friday 2.21.2025 Open Thread: An EcoHealth Alliance Collaborator in the new Trump White House — Why?

The above free vintage image of a meeting is courtesy of Masterfile and Google Images.

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. Today’s offering will discuss the appointment by President Donald J. Trump of Gerald W. Parker, Jr., DVM, PhD, to lead the White House Office of Pandemic Preparedness and Response Policy.

There are Important Wolf Moon Notifications, the Rules of our late, good Wheatie, and certain caveats from Yours Truly, of which readers should be aware. They are linked here.

Today’s offering has several aspects to the “tapestry of the whole.” There is much information. The first aspect begins here, with a CDC Health Advisory “requiring” hospitals to test patients hospitalized for influenza for the H5N1 Avian Influenza virus: https://merylnass.substack.com/cp/156773935, “CDC has issued a bulletin requiring hospitals to test for bird flu (H5N1) so they can find human cases and start the vaccine”, 9 February 2025. A screenshot of the title and secondary header for this article is below. Dr. Nass is a physician.

On 16 January 2025, a few days before the Inauguration of the former 45th President of the United States, Donald J. Trump, as the current 47th President of the United States, Donald J. Trump, the CDC (a department of Health and Human Services, HHS) issued the following Health Advisory regarding new, mandatory hospital testing for Avian Influenza H5N1 for all hospitalized influenza patients: https://www.cdc.gov/han/2025/han00520.html, “Accelerated Subtyping of Influenza A in Hospitalized Patients.” However, it appears that the Health Advisory is being used in ways to make look as if it were issued by the new Trump administration. Or so it seems. Please see below, from the article by Dr. Nass (AdventHealth is a hospital chain that has several facilities, including in Florida and in Wisconsin):

The opening paragraphs of the CDC Health Advisory, per the article by Dr. Nass:

The Health Advisory goes on to list and describe what H5N1 testing needs to be performed, and so on.

The second aspect is the appointment by President Trump, on 7 February 2025, of Gerald W. Parker, Jr., DVM, PhD, to lead the White House Office of Pandemic Preparedness in the new administration: https://www.cidrap.umn.edu/public-health/trump-names-one-health-expert-lead-pandemic-response-office, “Trump names One Health expert to lead pandemic response office”, 7 February 2025. This situation has also been described by Dr. Robert Malone, here (with thanks to our good scott467): https://www.malone.news/p/vaccine-deep-state-insanity, 14 February 2025. Let’s look at some details regarding Dr. Gerald Parker:

One: He has been involved with the Global One Health organization at Texas A&M University for years: https://onehealth.tamu.edu/about. Two: he has been involved with the CIDRAP program at the University of Minnesota for years: https://www.cidrap.umn.edu. CIDRAP stands for Center for Infectious Disease Research and Policy. Three: he has extensive involvement in teaching, in the military, and in global health initiatives: https://usacenter.tamu.edu/faculty-staff/gerald-parker.html. Please also see the information in Dr. Malone’s blog article, cited above. Four: he is involved with biodefense: https://biodefensecommission.org/teams/gerald-w-parker-jr-dvm-phd/. The organization https://biodefensecommission.org is a “non-partisan” group that is “Protecting U.S. public health security beyond party lines.” Five: he has testified before Congress regarding biodefense and public health. Here is the link to one of his testimony appearances, from 13 June 2023: https://d1dth6384htgma.cloudfront.net/Gerald_Parker_Witness_Testimony_06_13_23_4cc1c435d2.pdf?updated_at=2023-06-12T15:58:04.003Z. The title page for his prepared remarks to the House committee is below:

Below is a portion of his remarks, from page 27 (of 30) of his prepared statement for the House hearing. Notice the emphasis on federal government funding for university laboratories:

The Texas A&M story on this appearance is here: https://vetmed.tamu.edu/news/press-releases/parker-testimony-preparedness/, “Texas A&M’s Gerald Parker Testifies On Health Preparedness”, 26 June 2023.

The third aspect is about Global One Health, headquartered at Texas A&M University. Please see: https://onehealth.tamu.edu/about. Below is a screenshot of the “collaborators” involved with Global One Health:

Yes, you read that correctly: one of the “collaborators” with Global One Health is none other than EcoHealth Alliance. EcoHealth Alliance is now barred from receiving federal funds; and its president, Peter Daszak, has been fired: https://nypost.com/2025/01/18/us-news/hhs-bans-ecohealth-alliance-and-groups-ex-prez-from-receiving-federal-funding-for-5-years-after-wuhan-virus-experiments.

The fourth aspect is about CIDRAP itself: its Director, Michael T. Osterholm PhD. Please see: https://en.wikipedia.org/wiki/Michael_Osterholm. Dr. Osterholm founded CIDRAP at the University of Minnesota in 2001 and has been its Director ever since. Dr. Osterholm has been and/or is still involved with: the NIH; the World Health Organization; the FDA; the United States Defense Department; and, through CIDRAP, is a partner in the United States Department of Health and Human Services BioWatch Program since 2003. He has also been a member of the government’s COVID-19 Advisory Board since November 2020.

Among the funders of CIDRAP are: Gilead Sciences (Remdesivir), https://www.gilead.com/; and, Unorthodox Philanthropy (UP), https://unorthodoxphilanthropy.org/. UP appears to be a center-left / far-left funding organization.

The fifth aspect of this “tapestry” is about the “vaccines” now available against the H5N1 Avian Influenza virus. There are several H5N1 “vaccines” available for use in the United States. They are listed here: https://www.fda.gov/vaccines-blood-biologics/vaccines/vaccines-licensed-use-united-states, “Vaccines Licensed for Use in the United States”, current as of 14 February 2025. A screenshot of the current list of H5N1 “vaccines” is below:

AREPANRIX and AUDENZ are cell-based injectables. The Package Insert for AREPANRIX is here: https://www.fda.gov/media/182872/download. The Package Insert for AUDENZ is here: https://www.fda.gov/media/135020/download. For each of these, please read carefully regarding the Warnings and the Adverse Reactions listed and described in Section 5 and Section 6 of each product. (Note: the FDA is “reorganizing” its web pages. If either, or both, of the Package Insert documents do not load from the links above, use a search engine and type in “Package Insert for AREPANRIX” and/or “Package Insert for AUDENZ” in the search box.) The FDA Memorandum regarding the H5N1 “vaccines” in the National Stockpile is here: https://www.fda.gov/media/141737/download.

Yours Truly has written about the “new strain” of the H5N1 Avian Influenza virus, the “vaccines” available for this virus (for humans), and related topics. Please see: https://www.theqtree.com/2024/08/02/the-hhs-gave-the-go-ahead-to-use-an-h5n1vaccine-but-the-ama-just-issued-new-cpt-codes-for-an-h5n8-vaccine/; and, https://www,theqtree.com/2024/10/11/health-friday-10-11-2024-about-that-bird-flu-summit-this-month-in-virginia/.

But wait, there’s more! Did readers know that the USDA can issue “Conditional Licenses” for vaccines for animals and poultry? The USDA issued a “Conditional License” for an H5N2 Avian Influenza “vaccine” to be given to poultry, manufactured by Zoetis. And here’s where the story gets ** interesting **. First, the original press release by Zoetis on 13 February 2025 (https://www.zoetis.com/press-releases/press-release-details/2025/Zoetis-Receives-Conditional-License-from-USDA-for-Avian-Influenza-Vaccine/default.aspx):

Which Zoetis then followed up the next day with this press release: https://news.zoetis.com/press-releases/press-release-details/2025/Zoetis-Receives-Conditional-License-from-USDA-for-Avian-Influenza-Vaccine-H5N2-Subtype-Killed-Virus/default.aspx. This H5N2 Avian Influenza “vaccine” is to be used on chickens. Below is a screenshot from the 14 February 2025 press release:

Note the language regarding the “sole discretion” of “national regulatory authorities” (for example, the USDA) to “mandate” commercial poultry against Avian Influenza. Note also the “fact” that over “150 million birds in the U.S. have been affected with HPAI since February 2022.” The APHIS press release cited in the above is here, dated 20 June 2024: https://www.aphis.usda.gov/livestock-poultry-disease/avian/avian-influenza/hpai-detections/commercial-backyard-flocks.

Who at the USDA or the CVB (Center for Veterinary Biologics, a unit of the USDA) signed the “Conditional License” for the Zoetis Avian Influenza H5N1 “vaccine” on 13 February 2025? The new USDA Director, Brooke Rollins, was only confirmed for the office on 13 February 2025. Would Ms. Rollins have then immediately signed the “Conditional License” paperwork? Or — did a Biden administration holdover sign the paperwork? Let’s examine the situation:

On 13 February 2025, Brooke Rollins was confirmed as the new USDA Director. She took over on that date from the Acting Director, Gary Washington, a Biden administration holdover, who was the Chief Information Officer for the USDA.

On 13 February 2025, the top organizational flowchart for the USDA’s CVB (Center for Veterinary Biologics) looked like this (the chart is from 31 December 2024; Yours Truly cannot find a more recent one):

The CVB would have been the department that most likely signed off on the “Conditional License” for the Zoetis new “vaccine” for H5N2 that is to be given to chickens. Looking at the above chart, the person who signed off on this “vaccine” likely would have either David White, DVM (Biden holdover), the Director of the CVB; or, Bruce Thomsen, DVM (Biden holdover), the Virology Section Leader. On the other hand, a search via https://www.aphis.usda.gov/leadership (list current as of 22 January 2025) turns up at least two other possibilities: Michael Watson, PhD, (Biden holdover) the USDA Administrator; and, Rosemary Clifford, DVM, (Biden holdover) the USDA’s Chief Veterinary Officer.

What, in Yours Truly’s opinion, appears likely was that a Biden holdover at the USDA or the CVB signed the “Conditional License” of the Zoetis new H5N2 “vaccine” for chickens just before, or even perhaps on the day of, the confirmation of Brooke Rollins on 13 February 2025 as the new Director of the USDA.

But wait, there’s even more! — what appears to be another component of the “perceived threat” combined with gaslighting aspects regarding the “spread of H5N1 Avian Influenza among humans.” And, interestingly enough, the following article from CIDRAP (the organization “tied to the hip” with Gerald Parker, DVM) is dated 13 February 2025 — the day that Brooke Rollins was confirmed as the new Director of the USDA: https://www.cidrap.umn.edu/avian-influenza-bird-flu/cdc-3-veterinarians-had-recent-h5n1-infections-didnt-know-they-had-been, “CDC: 3 veterinarians had recent H5N1 infections but didn’t know they had been exposed”, 13 February 2025. The three veterinarians had been working with cattle when they were exposed to H5N1.

And, finally there is this: https://brownstone.org/articles/bird-flu-is-a-rerun-of-the-covid-playbook/, by Clayton J. Baker, MD, 18 February 2025. Below are screenshots from Dr. Baker’s article, beginning with his premise:

Followed by this:

And further followed by some of his recommendations:

Further: The AMA has just come out with a new CME (Continuing Medical Education) course offering: https://edhub.ama-assn.org/stanford-medicine-cme/audio-player/18944368, “Stanford Medcast Episode 89: Hot Topics Mini-Series: Insights and the Potential Global Impact of H5N1 Bird Flu”, 22 January 2025. This is an interview with Dr. Abraar Karan, MD, MS, MPH. There is an option further down on the webpage to listen to the transcript of the audio; click on “Read Transcript.” Dr. Karan covers various aspects of the current H5N1 situation. Among other items he talks about, Dr. Karan appears to be of the opinion that people should not drink raw milk, as it may contain elements of H5N1 from untested cows. He also appears to approve the testing and “vaccination” of poultry workers and dairy workers related to H5N1. In addition, he appears to be for mass testing of poultry and of dairy cows; and, for the federal government to be more “active” in coordinating and facilitating testing and “vaccination” of animals and humans regarding H5N1.

In Yours Truly’s opinion, it is still unclear as to whether or not there is (or, will be) an “H5N1 Avian Influenza pandemic” on the horizon. On the other hand, there appears to be an increasing amount of what may be seen as “perceived threat” gaslighting — from the federal government, the mainstream media, the AMA, and other entities. And, the issuance of the HHS Health Advisory that “requires” hospitals to test hospitalized influenza patients for Avian Influenza could be a “signal” that there may be the start of increasing pressure to get Americans “vaccinated” against this virus. In addition, also in Yours Truly’s opinion, this increasing pressure **may** be a method of “corralling” Americans to “get back onto the plantation” of obediently doing what the government wants / “mandates” them to do, which is what occurred, and with such success, during the declared COVID-19 pandemic. It has taken the American people almost five years to fully realize that the COVID-19 “vaccines” WERE NOT and ARE NOT “safe and effective”; to fully realize that mass lockdowns created economic chaos; to understand that standing six feet away from another person did not “stop the spread” of the virus; and so on.

Why is there now an EcoHealth Alliance “collaborator”, Gerald W. Parker, Jr., DVM, PhD, in the Trump White House? Why was Dr. Parker appointed to lead the White House Office of Pandemic Preparedness and Response Policy?

Paging Robert F. Kennedy, Jr. Paging Brooke Rollins.

THERE. MUST. BE. JUSTICE.

**** FLASH! ADDENDA Saturday 22 February 2025: via https://peterhalligan.substack.com/p/minnesota-declares-a-state-of-emergency, “Minnesota declares a State of Emergency over three strains of avian flu — 9 million more chickens under threat of a death sentence”, 22 February 2025. There is a link to the article on this situation at https://presidentialwire.com/minnesota-declares-state-of-emergency-over-bird-flu-outbreak/. Below is a screenshot from the Peter Halligan article, via Presidential Wire:

There is a tweet in the Presidential Wire article on the situation. The tweet is here: https://x.com/NewsNew97351204/status/1891557498265448685, dated 17 February 2025.

Below is a screenshot, again from the Halligan blog post via the Presidential Wire article, about GERALD W. PARKER, JR., DVM, PHD, having been appointed to lead the White House Office of Pandemic Preparedness and Response Policy:

And, guess what? There is a poultry testing laboratory at the University of Minnesota (a university that is “tied to the hip” with Gerald W. Parker, Jr., DVM, PhD — please see above in the original Health Friday post of Friday 21 February 2025): https://vdl.umn.edu/laboratories/minnesota-poultry-testing-laboratory (which Yours Truly suspects is the same type of BSL-2 safety level that is the case at the USDA Southeast Poultry Testing facility in Athens, Georgia.)

Yours Truly feels it is ** interesting ** that the state of Minnesota declared an Avian Influenza among chickens State of Emergency ** just after ** Dr. Parker was appointed to lead the White House Office of Pandemic Preparedness and Response Policy.

Peace, Good Energy, Respect: PAVACA

The HHS Gave the “Go-Ahead” to Use an H5N1″Vaccine”— But the AMA Just Issued New CPT Codes for an H5N8 “Vaccine”

The above image is of mass vaccination against smallpox in Paris in 1905. (Courtesy, Getty Images.)

Today’s post will trace what ** may be ** a “sleight-of-hand” that started out with Xavier Becerra, the Secretary of the United States government Department of Health and Human Services, giving the “Go-Ahead” for the use of the H5N1 Avian Influenza “vaccine”, AUDENZ, in anticipation of a potential “bird flu pandemic” in the United States; but, which since has been “transformed” into the American Medical Association just issuing new CPT codes for an Avian Influenza “vaccine” for a different strain, called H5N8. Meanwhile, the CDC / FDA / United States government, are all sending out warnings related to the H5N1 strain. Stay with Yours Truly, it gets even better — “Mais, mon Dieu!” — the twists and turns! This post is a kind of “snapshot” of the situation — it is an evolving issue.

For purposes of today’s post, the trail begins here: www.ernst.senate.gov/imo/media/doc/fowl_play_squeal.pdf, the letter that Sen. Jodi Ernst (R-Iowa) sent to USDA Secretary Tom Vilsack on 14 February 2024. In this letter, Sen. Ernst demands answers regarding United States government funding of what appears to be Gain-of-Function research experiments on Avian Influenza viruses; which experiments involve a scientist linked to the Chinese Communist Party. Yours Truly can find to date, no response from Sec. Vilsack to Sen. Ernst. A screenshot of Page 1 of her letter is below:

Yours Truly now turns to this: www.aha.org/news/headline/2024-07-23-hhs-broadens-emergency-declaration-facilitate-response-bird-flu-other-viruses-pandemic-potential, “HHS broadens emergency declaration to facilitate response to bird flu, other viruses with pandemic potential”, dated 23 July 2024, which “expanded” the 2013 amendment to the Federal Food, Drugs, and Cosmetics Act to now include “other viruses” that may have “pandemic potential.” The document, from HHS Secretary Xavier Becerra, specifically mentions three types of Avian Influenza strains: H1N1 (from 2009); H7N9 (from the 2013 amendment);, and H5N1 (from the 24 March 2024 USDA statement regarding H5N1 infections in dairy cows in Kansas and in Texas.) https://public-inspection.federalregister.com/2024-16247.pdf. Below is a screenshot from the AHA (American Hospital Association) press release:

And, for reference, here is the Congressional Research Service Legal Sidebar document related to what the HHS Secretary can “declare” under the PREP Act (including removing liability options), updated 21 July 2023: https://crsreports.congress.gov/product/pdf/LSB/LSB10730, “The PREP Act and COVID-19, Part 2: The PREP Act Declaration for COVID-19 Countermeasures.”

This was followed by a tweet from Robert Kennedy, Jr.: https://twitter.com/RobertKennedyJr/status/1816905031653675473, a screenshot of which follows:

Meanwhile, the USDA had already issued a press release regarding how dairy farmers can apply to receive expanded livestock assistance to compensate for milk production lost due to their cows infected with H5N1: www.usda.gov/media/press-releases/2024/06/27/usda-begin-accepting-applications-expanded-emergency-livestock, “USDA to Begin Accepting Applications for Expanded Emergency Livestock Assistance Program to Help Dairy Producers Offset Milk Loss Due to H5N1”, dated 27 June 2024.

Which was followed, in turn, by a CDC release regarding the government’s response to the current H5N1 Avian Influenza situation: www,cdc,gov/bird-flu/spotlights/h5n1-response-07262024.html; a screenshot from the release is below:

So, it would appear that the HHS gave the “go-ahead” for a kind of “EUA” regarding the use of the protein-subunit H5N1 “vaccine”, AUDENZ (a supply is already in the National Vaccine Stockpile); and, for the increased production of this “vaccine.” What follows is a “closer look” at AUDENZ. Yours Truly will begin with the FDA-issued Fact Sheet for healthcare providers for this “vaccine”: www.fda.gov/media/135020/download; three screenshots from the document are below. The first screenshot shows clearly that there was no Placebo group (Control/saline group) in at least two clinical trials for AUDENZ. The second screenshot shows clearly that no Toxicology studies were performed for AUDENZ. The third screenshot is Page 10 of the Fact Sheet.

Note this language in the first screenshot: “In both Studies 1 and 2, all SAEs appeared unrelated to study treatment.” This indicates at least two important details: One, that Serious Adverse Events (SAEs) did occur during at least two clinical trials of AUDENZ; and, Two, that these Serious Adverse Events were not considered to be related to the clinical trials for AUDENZ. This is the same type of language that Pfizer-BioNTech used regarding Serious Adverse Events that occurred during the (shortened and data-compromised) clinical trials for the company’s “flagship” COVID-19 modRNA “vaccine” BNT162b2. Note also that a “complete dose series” for AUDENZ is two separate doses of 0.5mL each, for all age groups age six months and up. AUDENZ uses an adjuvant (an ingredient that facilities the activities of the injectable) called MF59. MF59 is a squalene-based, oil-in-water adjuvant. The Safety Data Sheet for MF59 is here: https://file.medchemexpress.com/batch_PDF/HY-153206/MF59-SDS-MedChemExpress.pdf. The product is listed as “Not a hazardous product or mixture” in section 2.2 of this document. However, reading further down the same document, one finds all sorts of contradictory information in the sections on “First Aid Measures”, on “Handling and Storage”, on “Exposure Controls”, and more.

Note also the list of reported adverse events in section 6.2 of Page 10, above. These are same types of adverse events reactions to the Pfizer-BioNTech modRNA COVID-19 “vaccine”, BNT162b2, in the post-authorization report that this company gave to the FDA on 30 April 2021; and in reports to VAERS; and, which are listed within the FDA-issued Fact Sheet for Healthcare Providers for the “2023-2024 Formula COVID-19 Vaccine” by Pfizer-BioNTech (www.phmpt.org/wp-content/uploads/2022/04/reissue_5.3.6-postmarketing-experience.pdf; www.openvaers.com/; www.fda.gov/media/167211/download?attachment. Very troubling are the listings in section 6.2 of Page 10 above in the AUDENZ fact sheet for “convulsions”; “demyelination”; “encephalitis”; and, “Guillain-Barre’ syndrome.”

A blog post by Dr. Jessica Rose, PhD, on 27 June 2024, presents a summary of clinical trial for AUDENZ (NCT02839440), in which she proves that the fatality rate is 1/200 chances for AUDENZ: https://jessicar.substack.com/p/1200-chance-of-death-in-context-of, “1/200 chance of death in context of new bird flu injection – 5 times higher than placebo according to clinical trial.” NCT02839440 did have a Placebo control group, (Scroll down the blog post to the discussion of this clinical trial for AUDENZ.)

To date, Yours Truly can find no exact set of CPT Codes for AUDENZ. The closest item found is here: www.hhs.gov/guidance/document/flu-shot-coding-0; the listing is “Q2039 Influenza virus vaccination otherwise specified.”

AUDENZ is produced by CSL Seqirus, part of the much-larger CSL multinational drug company. Following is a JPG of the list of CSL offices and locations, sourced from: www.csl.com/:

The United States government awarded CSL Seqirus a contract to produce millions of doses of an Avian Influenza “vaccine” in May 2024: www.cslseqirus.us/news/csl-seqirus-announces-us-government-award-in-response-to-avian-influenza. The “vaccine” will be manufactured by the CSL Seqirus facility at Holly Springs, North Carolina. This facility was built in partnership with BARDA (Biomedical Advanced Research and Development Authority), a department of the United States government. The Avian Influenza “vaccine” that this facility will manufacture is “cell-based”, as opposed to “egg-based”; with a six-month “turnaround” for production: www.csl.com/we-are-csl/our-business-and-products/csl-seqirus/csl-seqirus-manufacturing-technologies. Below are two images from the article related to this facility:

Note that whatever Avian Influenza cell-based “vaccine” from the CSL Seqirus facility at Holly Springs will use the MF59 adjuvant. (By the way, MF59 is trademarked by Novartis AG, which was acquired by CSL.)

So far, it appears that the H5N1 strain of Avian Influenza is the one that the United States government is focused upon. However, here’s where the trail veers to another path.

Please refer back to the American Hospital Association press release above in today’s post. Note this language: “The amendment now applies to pandemic influenza A viruses and others with pandemic potential, such as the current H5N1 strain of bird flu…” (Italics, Yours Truly) In Yours Truly’s opinion, this is “a hole big enough to drive a truck through” — or, perhaps, another strain of Avian Influenza.

The following article beings to “lift the curtain” on what ** may ** really be going on — which, again in Yours Truly’s opinion, appears to be a kind of “sleight-of-hand”: www.naturalnews.com/2024-07-26-fda-grant-eua-mrna-bird-flu-vaccines.html, “Pandemic 2.0 ready to go: FDA to grant emergency use authorization (EUA) to mRNA bird flu shots, just like what happened with COVID“, by Ethan Huff. And, “right out of the gate”, the article begins with this:

But, wasn’t the “upcoming potential bird flu pandemic” supposed to be the H5N1 strain that the government is warning about? Where does the H5N8 strain come in? According to Wikipedia, the H5N8 strain of Avian Influenza is “is typically not associated with humans.” https://en.wikipedia.org/wiki/Influenza_A_virus_subtype_H5N8. Very few humans have contracted a case of H5N8; this virus strain predominates among wild birds. However, the mortality rate among wild birds infected with H5N8 is “at least 75%”, again according to the Wikipedia article above.

Now, turning to the American Medical Association’s issuing new CPT Codes for the use of an H5N8 “vaccine.” One media outlet that Yours Truly found has this: https://revcycleintelligence.com/news/ama-updates-cpt-code-set-for-avian-influenza-vaccines, dated 22 July 2024. Below is a screenshot from the article, with the new CPT codes:

Note that the American Medical Association owns the rights for the CPT codes. This means that the AMA gets a “royalty payment” every time a CPT code is used. The AMA notice regarding the CPT codes for H5N8 is here: www.ama-assn.org/press-center/press-releases/ama-announces-cpt-update-avian-influenza-vaccines, dated 19 July 2024. Below is a screenshot from the notice:

What’s going on here? The picture is, to say the least, somewhat “murky.” There are, however, a few potential clues. Among them is this: www.pennmedicine.org/news/news-releases/2024/may/penn-researchers-develop-experimental-mrna-avian-flu-vaccine, dated 23 May 2024. Note on the screenshot, below, from the article, the language regarding “a specific type of the H5N1 virus”; and, that animals other than wild birds were being used for the experiments:

Here is another clue, from 5 June 2024: www.idsociety.org/science-speaks-blog/u.s.-orders-4.8-million-doses-of-a-cell-based-adjuvanted-h5-vaccine-for-avian-flu-preparedness#/+/0/publishedDate_na_dt/desc/, by Daniel R. Lucey, MD, PhH, FIDSA. Below is a screenshot from this article:

Note the language regarding “pre-pandemic vaccine that is well-matched to the H5 of the currently circulating H5N1 strain,…” (bolding, Yours Truly)

A third clue is here: https://twitter.com/RenzTom/status/1816110256843264368; a screenshot of part of his tweet is below:

And, a fourth clue is here: https://clinicaltrials.gov/ct2/show/NCT05874713, a clinical trial that appears to be in the “wrapping-up” stages regarding testing an mRNA-based H5N8 “vaccine.” Below is a screenshot from the Clinical Trials webpage for this clinical trial:

Note the very low test subject enrollment (480 persons); the presence of the MF59 adjuvant in the H5N8 “vaccine” candidate used in the clinical trial; and, a “two-dose” series of “primary run” injections of the “vaccine” candidate, followed by a “booster shot” on Day 209 for the H5N8 “vaccine” candidate.

There are three other clinical trials of an H5N8 “vaccine” listed on the https://clinicaltrials.gov/ website: NCT02624219 (Completed); NCT05975840 (Active); and, NCT03014310 (Completed.) All of these clinical trials were/are Phase I or Phase I/II. None of them have a Placebo/saline control group. Each of them have fewer than 600 subjects (NCT02624219 had 275 test subjects.) Two of these three other clinical trials have the NIAID as the Sponsor.

What does all this mean? Is it possible that the current H5N1 “Avian Influenza infecting cattle, cows, and domesticated pets, in addition to poultry” situation, while it is indeed occurring, is also a sort of “Look, squirrel!” to distract from something that may be more dangerous?: from, perhaps, Gain-of-Function experiments on the H5N8 strain of the Avian Influenza (recall that this strain has a 75%+ mortality rate among the wild birds that it infects); plus, perhaps. the development of “vaccines” for this “perhaps-enhanced” H5N8 strain, which may include the millions of doses of an “Avian Influenza cell-based vaccine” that will be manufactured at the CSL Seqirus facility in North Carolina? In other words, “Pandemic 2.0”?

Good Energy, Peace, Respect: PAVACA