“We do not believe any group of men adequate enough or wise enough to operate without scrutiny or without criticism. We know that the only way to avoid error is to detect it, that the only way to detect it is to be free to inquire. We know that in secrecy error undetected will flourish and subvert.” –J. Robert Oppenheimer
The free header image of a “swirl clock” for today’s offering is courtesy of 123RF and Google Images.
Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics.
There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: Yours Truly has checked today’s offering for AI-generated content. To the best of her knowledge and belief, there is none. If readers wish to post AI-generated content in today’s discussion thread, they must cite their source. Thank you.
Charlie Kirk, conservative activist, commentator, husband and father, was assassinated on Wednesday of this week (10 September 2025) as he was speaking at a “Prove Me Wrong” debate and rally at Utah Valley University in Orem, Utah. He was shot on the left side of his neck by a sniper who fired from approximately 200 yards away. It appears that the sniper’s single shot fired hit Mr. Kirk’s carotid artery. Mr. Kirk was pronounced dead at the hospital to which he was rushed after the hit. He leaves behind his wife, their two very young children, his parents, other relatives, and many friends. He leaves behind his work with Turning Point USA (TPUSA, of which he was the founder and chairman), and his other endeavors (his Salem Media Group talk show, his social media activities, and so on.) May Charlie Kirk rest in eternal Peace; and may the Almighty God sustain his widow and young children. May the assassin be found, along with those who recruited him. May Justice be meted out to them.
The cold-blooded, planned assassination of Charlie Kirk was Evil In Our Time. Make no mistake about this.
Today’s offering is not about the COVID-19 disaster: it is about the potential for a “new pandemic on the horizon”: H5N1 (Avian Influenza), another Evil In Our Time. Yours Truly has written about this situation in other Health Friday posts. Today’s post regards the latest Evil In Our Time news related to this issue: the lab-creation of TWO new chimeric types of H5N1 virus by the Chinese Communist government-owned company, Sinopharm. The first of these new, lab-created chimeric H5N1 viruses “attaches” to host cells at a rate 64 times higher than other strains of H5N1 viruses; the second of these new, lab-created chimeric H5N1 viruses has a “kill rate” of 100% in lab animals.
The story is here: https://jonfleetwood.substack.com/p/china-lab-engineers-two-new-bird, “China Lab Engineers Two New Bird Flu Constructs: One Binds to Host Cells 64x Stronger, the Other is 100% Lethal in Mammals”, Jon Fleetwood, 8 September 2025. Please see the screenshots from this article, below:
The paper published by the Sinopharm scientists who performed the work is here: https://doi.org/10.1016/j.virol.2025.110672, “H5N1 influenza virus-like particles based on BEVS induce robust functional antibodies and immune responses”, Yongbo Qiao, et al., 29 August 2025.
The Sinopharm scientists actually did two things: First, they lab-created two new, chimeric types of H5N1 virus that would guarantee either “attachment” to host cells at a rate 64 times higher than current H5N1 strains; or, would be lethal 100% of the time. Then, Second, they lab-created a “VLP-based vaccine” that would “induce robust functional antibodies and immune responses” to the said two new, chimeric H5N1 viruses. Please see the screenshots of the Abstract from this paper, and the Graphical Image from this paper, below:
Note that “Antigen presentation in lymph node” is the attack by these lab-created new, chimeric H5N1 viruses on the CD4 – CD8 T cells in the lymph nodes— the same things that the SARS-Cov-2 (COVID-19) virus itself, and the COVID-19 ‘vaccines”, do. Proper function of the CD4 – CD8 T cells is crucial to proper function of the human immune system in general.
This type of state-sponsored and state-funded Gain-of-Function work is Evil In Our Time. It’s not so much “the advancement of science.”
By the way, the Sinopharm lab where the work was performed is a BSL-3 lab — like the ones in many other bioweapons labs, and in university labs (like the Baric Lab at UNC, Chapel Hill.) http://en.sinopharm.com/2023-02/c_18829.html, 24 February 2023 (Sinopharm R&D webpage — be aware, it’s not secure.)
ALL GAIN-OF-FUNCTION WORK, NO MATTER WHERE IT IS PERFORMED, AND NO MATTER ON WHAT, MUST BE STOPPED. NOW. ALL EFFORTS TO MOUNT A “NEW PANDEMIC” OF H5N1, NO MATTER OF WHAT STRAIN, MUST BE STOPPED. NOW.
The featured vintage image of a laboratory for today’s offering is courtesy of iStock and Google Images.
Health Friday is a series devoted to information about Big Pharma, vaccines, general health, and associated topics.
There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: Yours Truly has checked today’s offering for any AI-generated content. To the best of her knowledge and belief, there is none, except perhaps for AI-generated images in links included in today’s post. If readers wish to add any AI-generated content to the discussion thread today, they must cite their source. Thank you.
Today’s offering is about the “under-the-table” work, the “being performed but under another name” work, the “grandfathered-in” work, of Gain-of-Function (GoF) experiments that are onoing. These GoF experiments involve experiments with mRNA-based platforms; with “inactivated virus” platforms; and, with “novel delivery” platforms.These GoF experiments are being funded by “private Big Money”; and, by the United States government (in other words, with taxpayer money.)This post is long; please bear with me.
It is now well-known that the COVID-19 disaster was a product of GoF experiments, of two types: One, the GoF work that was performed in various labs (the Baric Lab at UNC, Chapel Hill; the Wuhan Institute of Virology, Wuhan, Communist China; the United States Army biological weapons labs at Ft. Detrick, Maryland, among others.) And, Two, the GoF work that was performed using the lab-created Wuhan Hu1 SARS-CoV-2 virus itself as the foundation for the modRNA (aka mRNA) COVID-19 “vaccines” that were developed by numerous companies, among them: PfizerUSA (at the company’s Pearl River, New York, facility; and, at other facilities); and, BioNTech (Mainz, Germany); Moderna (with the NIAID in Bethesda, Maryland, and at other facilities) — for use in the United States and also world-wide. (Note: PfizerUSA and BioNTech are separate companies that operate as a “joint venture” called Pfizer-BioNTech. PfizerUSA and BioNTech each have a separate CEO [Chief Executive Officer].)
Regarding the first Jon Fleetwood article: The 260 study subject children were living in South Africa, and were between the ages of 10 and 18 years. They were confirmed by to be HIV-negative at the time they were added to the study subject pool. They were injected with the Danish tuberculosis vaccine BCG1331 strain (Bacille Calmette-Guerin). The Package Insert for this vaccine is here: https://nibsc.org/documents/ifu/07-270.pdf. The BCG1331 strain is the Mycobacteriumbovis strain, which causes tuberculosis in cattle and can also cause the disease in humans, especially in HIV-compromised persons. Please see the screenshot from the Fleetwood article, below:
The paper that resulted from the study is here: https://doi.org/10.1056/NEJMoa2412381, “BCG Revaccination for the Prevention of Mycobacterium tuberculosis Infection”, Alexander C Schmidt, et al., 8 May 2025. Please see the screenshot from this paper, below:
In other words, 260 children now have tuberculosis because of the BCG1331 strain vaccine that they were injected with. And that Bill Gates funded this “human guinea-pig experiment.” But there’s more — the Fleetwood article also describes the Bill Gates-fundedMycobacterium bovis experiments at the University of Texas, performed in 2012, that resulted in a what may be called a “turbo-charged Gain-of-Function” version of this tuberculosis bacterium. The paper that was published from the 2012 study is here: https://doi.org/10.1016/S1472-9792(13)70007-6, “Mycobacterium tuberculosis MtrAY102C is a gain-of-function mutant that potentially acts as a constitutively active protein”, Akash T Satsangi, et al., published December 2013.
Regarding the second Fleetwood article: Another Bill Gates-funded effort, this time about a lab-created chimeric polio oral “vaccine” that was tested on human subjectsin the United States. The study results are nothing short of terrifying. Please the screenshot from the Fleetwood article, below:
There was a 100% incidence of “shedding” of this lab-created chimeric oral polio “vaccine.” Six human subjects were released from the study when it was found that testing of their stool showed they had possibly contracted the oral vaccine virus from other study subjects. Several human subjects had severe adverse reactions to this lab-created chimeric oral polio “vaccine.” This lab-created chimeric oral polio “vaccine” caused “unexpected” interactions with the type 2 poliovirus.
The team that lab-created this chimeric oral polio “vaccine” were from medical centers across the United States, including: University of North Carolina, Chapel Hill; University of Vermont; and, Dartmouth. The paper that was published from the study is here: https://www.thelancet.com/journals/laninf/article/PIIS1473-3099(25)00285-3/fulltext, “Safety and immunogenicity of novel live attenuated type 1 and type 3 oral poliomyelitis vaccines in healthy adults in the USA: a first-in-human, observer-masked, multicentre, phase 1 randomized controlled trial”, Laina D Mercer, PhD, et al., 13 August 2025. The clinical trial for this lab-created chimeric polio virus “vaccine” is listed here: https://clinicaltrials.gov/study/NCT04529538. Again, from the Fleetwood article:
Regarding the third Fleetwood article: Bill Gates has funded the creation of a new technology, called “SLIM microneedle”, which injects “microcrystals” of a contraceptive drug (levonorgestrel) into the body of a female; and, which microcrystals then”self-assemble” into an “implant” inside her body. Please see the screenshot from the Fleetwood article on this situation, below:
This type of “self-injected, self-assembly inside the body” approach has profound implications. Please see below, again from the Fleetwood article:
The paper that was published on this issue is here: https://www.nature.com/articles/s44286-025-00194-x, “Self-aggregating long-lasting injectable microcrystals”, Vivian K. Feig, et al., 24 March 2025. Note how “self-assembling” has magically become “self-aggregating” — in some attempt to hide the fact that the microcrystals really do “self-assemble?”
The SLIM “delivery system” for the contraceptive levonorgestrel (called “LNG” in the paper above) uses a solvent called Benzyl Benzoate (called “BB” in the paper above.) The paper describes the experiments performed to find the “right combination” of levonorgestrel + Benzyl Benzoate to create the SLIM delivery system — the “winning delivery system candidate” was named “LNG-BB.” Benzyl Benzoate is clearly dangerous. Part of Section 4 FIRST AID MEASURES from the MSDS Safety Sheet on Benzyl Benzoate from Spectrum Chemical (https://www.spectrumchemical.com/) is below:
And this is the “long-lasting solvent” that is used in the SLIM microneedle “self-aggregating” delivery system for levonorgestrel. Which means that this solvent will be acting in the body of the female who uses this delivery system for this drug for an (undetermined) amount of time.
Now, on to a recent GoF experiment, this one funded by NIH / NIAID, at the University of Pittsburgh. This GoF experiment resulted in the lab-creation of a chimeric H5N1 Avian Influenza virus strain that could infect dairy cattle. Jon Fleetwood wrote about this situation, here: https://jonfleetwood.substack.com/p/nih-funded-pennsylvania-researchers, “NIH-Funded Pennsylvania Researchers Build New Frankenstein Bird Flu Virus: ‘Journal of Virology'”, 26 August 2025. Vesicular stomatitis virus (VSV) is a virus that infects horses and cattle. In humans, Stomatitis infection can result in HSV-1 (the “cold sore” virus: per https://my.clevelandclinic.org/health/diseases/stomatitis-oral-mucositis.) However, the researchers at the University of Pittsburgh concentrated on “splicing” an element of VSV with H5N1. The paper that was published from this experiment is here: https://doi.org/10.1128/jvi.00621-25, “Dairy cattle herds mount a characteristic antibody response to highly pathogenic H5N1 avian influenza viruses”, Kevin R. McCarthy, et al., 25 August 2025. Please see the screenshots from the Fleetwood article on this issue, below:
Isn’t it “convenient timing” that this “new, chimeric VSV + H5N1 virus” comes on the heels of the announcement by the White House on 5 May 2025, that Gain-of-Function research would be stopped — but it appears that “certain contracts” would be permitted to “finish out”? And, that one of those “certain contracts” is with Arcturus Therapeutics for its self-amplifying RNA (saRNA) Avian Influenza “vaccine”, ARCT-2304? The White House announcement is here: https://www.whitehouse.gov/presidential-actions/2025/05/improving-the-safety-and-security-of-biological-research/. The news release related to the second quarter 2025 financial update and “pipeline progress” for Arcturus Therapeutics in which ARCT-2304 is mentioned, is here: https://www.biospace.com/press-releases/arcturus-therapeutics-announces-second-quarter-2025-financial-update-and-pipeline-progress, 12 August 2025. The clinical trial for ARCT-2304 is registered here: https://clinicaltrials.gov/study/NCT06602531; which, by the way, has NO saline-only Placebo control group; the only “control groups” in the study will be injected with a “control vaccine” or a “placebo vaccine” (which last, in and of itself, is not a true Placebo.)
And now, regarding something else: the GoF experiments that resulted in the lab-creation of an Avian Influenza “vaccine” which is a “Cocktail of Inactivated Avian Influenza Viruses”, a patent owned by Dr. Jeffery Taubenberger, a “career medical employee” of HHS and the federal government, and who is also the current Acting Director of the NIAID (National Institute of Allergy and Infectious Diseases, previously headed by Dr. Anthony Fauci), and who now is in control of the $500 Million dollars that was pulled from mRNA research activities in May 2025.This “bird flu vaccine cocktail” contains BPL (Beta-propiolactone), a known carcinogen.
The NIH TechTransfer information on this “cocktail” invention by Dr. Taubenberger is here: https://www.techtransfer.nih.gov/tech/tab-3388, “Broadly Protective Influenza Vaccine Compromising a Cocktail of Inactivated Avian Influenza Viruses”. Sounds “benign,” yes? Until one starts reading the actual Patent document itself, found here: https://image-ppubs.uspto.gov/dirsearch-public/print/downloadPdf/11369675, filed 21 July 2020. The following are screenshots from the Patent document:
Note it appears that Dr. Taubenberger was experimenting with as many as sixteen different strains of Avian Influenza to lab-create his “cocktail vaccine.”
Note it appears that Dr. Taubenberger is perfectly all right with “vaginal” and “rectal” administration of his “cocktail vaccine.”
Note that the Patent was registered in July 2020 — which can only mean that work on the experiments to lab-create this “Avian Influenza cocktail vaccine” must have begun at least nine months earlier. This would place the commencement of the experiments around October 2019 — just before the COVID-19 original virus was unleashed on on the world.
And THIS ingredient is part of the “Avian Influenza Cocktail Vaccine” of Dr. Jeffery Taubenberger, two possible methods of administration of which are INTRANASAL or INHALED, per the Patent document images above?
It is not enough that HHS Secretary Robert F. Kennedy, Jr., terminated 22 contracts for mRNA research in May of this year, but allowed “certain contracts” for mRNA (and saRNA) research to “finish out.” It is not enough that the White House announced a ban on Gain-of-Function research, since this type of research is still going on — funded by “private Big Money”, and/or by the NIH / NIAID (in other words, the United States government). The entire Gain-of-Function situation must be stopped, from all funding sources and on all levels of research and experimentation — until there are clear, firm, and enforceable regulations and restrictions on who can perform this type of research; that such research can only be permitted under strict circumstances; that such research must be under tight supervision; and, that such research can only be performed where there is a clear need in the area of public health —not what amounts to a “chimeric fishing expedition” to lab-create viruses. It is time for any and all “go-along-to-get-along” activities to stop — such as, bowing to the “demand” by Sen. Dr. Bill Cassidy for his “cooperation” in “working with” HHS as regards hiring, or anything else. By the way — Sen. Dr. Cassidy has received donations from multiple pharmaceutical entities (United Health, AstraZeneca, Pediatrix Medical Group, and so on: per Open Secrets (https://opensecrets.org/.) And — that the further development of the above-discussed “Avian Influenza Cocktail Vaccine” must be stopped.
HHS Secretary Kennedy, Jr.: Please understand that the “career medical bureaucrats” in the CDC, the FDA, and the other divisions of the HHS, are not inclined to your views. They want “the good old days” of these divisions brought back. They are working “behind the scenes” in some instances, and in other instances, out in the open, to obstruct, delay, and thwart your efforts to clean up HHS and “re-tool” the department to reflect Make American Healthy Again. There is even what may be called “soft interference” by persons not employed by HHS such as, Sen. Dr. Cassidy.
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.
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 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:
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.
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.
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 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.
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.
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.”
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.
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.
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:
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”?
