The Value of “Expected Value”

(Once Again, an excellent article by  A MIDWESTERN DOCTOR.  I am including only a part of the article.  Check out the link for the rest.)

The Critical Calculation Medicine Won’t Make

How a simple framework reveals that “proven” therapies often lack value while the “unproven” ones lack only approval

Story at a Glance:

  • As decisions always have pros and cons, making the correct one is often quite challenging. One framework, “expected value” (EV), solves this puzzle by calculating the relative probability of a good (positive) and bad (negative) outcome.
  • In medicine, while frameworks like EV should be used to guide medical policies and clinical decisions, they frequently are not, resulting in practices like mass COVID vaccination which have explicitly negative EVs being adopted and then held to regardless of public pushback or evidence to the contrary.
  • Much of this stems from our widespread societal faith that large randomized controlled trials (RCTs) are the definitive arbiter of scientific truth, despite their numerous shortcomings. In contrast, valid and affordable approaches for determining scientific truth are continually marginalized, making it nearly impossible to “prove” competing therapies work or that sanctioned therapies have serious harms.
  • Much of this originated from two subjective linguistic interpretations which the FDA then used to prohibit the public’s access to life-changing (but non-commercializable) therapies like DMSO and protect its industry sponsors—which as DMSO stories in this article show, has created profound consequences that have been well-hidden from all of us.
  • This article will explore how this dysfunctional dynamic has harmed the health of America, meaningful changes that could preserve the vital functions of the FDA while simultaneously preventing it from sabotaging America’s health, and the changing political winds we’ve helped create which are gradually forcing those changes to happen.

The majority of decisions in life aren’t clear cut as they have both an upside and a downside (or multiple upsides and downsides). However, rather than being fully cognizant of the complexity of the decision, the human mind will typically narrow the picture and see only one side of the coin to reduce this large cognitive load. Many perpetually unresolved political conflicts essentially result from this, as each side emotionally primes their adherents to focus on the arguments in favor of their position and those which undermine the other side, resulting in both sides having a view of reality where their side is correct and the other is irredeemably wrong—which in some cases holds true, but typically is not.

One of my favorite frameworks for encapsulating this paradigm is the biostatistics concept of “sensitivity and specificity,” which denote how likely a test is to catch something that is there (sensitivity) and how likely it is not to overshoot and only identify things that are actually there (specificity). The value of this framework (beyond providing an informed way to choose medical tests) is that it emphasizes the reciprocal relationship between the two, as if one is increased (e.g., more aggressively screening for something), the other decreases (e.g., that screen will have a higher rate of false positives).

Because of this, ideally, the sensitivity and specificity of a test (and what will then be done with either result) should be appropriate to a patient’s clinical situation and in parallel, work is always done to improve the tests themselves so better balances between sensitivity and specificity can be met. In contrast, in overly politicized issues (e.g., criminal justice), the focus always ends up being on maximizing sensitivity OR specificity rather than finding a reasonable compromise between the two, which maximizes both as much as is feasible.

However, the reality is that you will frequently be confronted with situations where there is a less than ideal balance of upsides and downsides (e.g., sensitivity and specificity) between the two options, but a choice nonetheless must be made. Fortunately, due to how common these situations are, effective decision making strategies have been developed and refined.

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Predicting Expected Values

The classic mathematical formula used to “solve” these situations is expected value (EV), which essentially calculates “on average, how much will this situation benefit or harm me.”

This translates to (magnitude of outcome 1 * probability of outcome 1) + (magnitude of outcome 2 * probability of outcome 2), and this is repeated for all possible outcomes (e.g., it could go to calculating outcome 10) so that the total probabilities add up to 1. So for example, if you had a situation where you paid a dollar to flip 2 coins and then got 99 cents for each “heads” you got, the EV for the four outcomes (HH, HT, TH, TT) would be (1.98*0.25)+(0.99*0.25)+(0.99*0.25)+(0*0.25) or $0.99. Given that your cost to play this game is $1.00, it is hence “not a good idea” to play the game as there is a negative DV (on average you will lose money).

Many businesses (beyond just casinos), in turn, are essentially structured so that the EV of the transactions they make are positive for them (and negative for the customer) hence (excluding highly unusual circumstances) ensuring a steady stream of profit which sustains the business or industry.

While everyone has a general grasp of EV (e.g., if you saw a dollar bill fly into the freeway, almost no one runs onto the highway to try to grab it as the risk of being hit by a car makes the EV very bad there), a few points are critical to understand about it:

First, most people do not have a strong grasp of probabilities, and as such, predatory industries will frequently mislead them about the actual probabilities, leading them to believe bad EV choices are actually good EV choices.

Second, rather than being a simple binary calculation, EV calculations are often complicated because there are many potential outcomes (variables).

Third, EV can encompass a variety of outcomes beyond financial gains or losses, at which point it becomes harder to fit into a numerical formula.

For example, many of the policies that were pushed on us during COVID-19 essentially arose from people being implicitly presented with erroneous EV formulas by the mass media, and then extrapolating decisions off those formulas which appeared beneficial (positive EV) but in reality were harmful (negative EV) with a correct formula.

To illustrate, the odds of a child dying from COVID-19 were effectively 0 (and in the small number who died, there was almost always a severe underlying condition), so no real benefit could be derived from vaccinating, whereas injuries (including fatal ones) routinely occurred. So, the EV of a child taking the COVID vaccine was always negative (as there was no “positive” outcome, whereas a negative one could occur).

Likewise, when the Pfizer NEJM paper came out (which made many, including most of the medical profession, decide they had to get the vaccine no matter what since it was “95% effective!” and would end the pandemic), the paper itself stated:

  1. Adverse reactions were much more common in the vaccine than the placebo group (27% vs 12% for a direct event and 21% vs. 5% for an unrelated adverse event)
Similar reaction rates were reported in the other age groups. Additionally, “severe fatigue” was reported in 4% of recipients.
  1. In contrast, for COVID infections, those same symptoms occurred, typically 1-2 times as frequently (sometimes 3x).
  2. 8/18,198 (0.044%) vaccinated developed COVID and 162/18,325 (0.88%) of the unvaccinated developed COVID (a 20-fold decrease).
  3. Seven days after the initial dose, 1/18,198 vaccinated and 9/18,325 unvaccinated developed severe COVID (COVID typically requiring hospital care).
    Note: this metric was changed to after the first vaccine (whereas the primary efficacy measurement ones were after the second vaccine), since 5 of the severe infections in the placebo group happened prior to the seven day post vaccine cut-off (which was hidden in the appendix). Had this standard been used for all COVID infections too, it would have been (39+8)/18,198 vs. (82+162)/18,325 (a 5.16 fold decrease falling far short of the “95% effective” benchmark), whereas had the study’s primary criteria been used here, it would have been 1/18,198 vs. 4/18,325 (a 4-fold rather than 9-fold decrease)—illustrating how studies always change their metrics and criteria in whatever manner makes the product look best.
  4. 4 serious adverse events attributed to vaccination were reported (shoulder injury from injection, right axillary lymphadenopathy, paroxysmal ventricular arrhythmia, and right leg paresthesia).
  5. 2 vaccine recipients died and 4 placebo recipients died (all from causes unrelated to COVID-19).
  6. Nothing in this study evaluated transmission.

When I read this paper, I was jaw dropped, as it was blatantly stating there was an extremely negative EV for the vaccine as you were trading the symptoms from a COVID infection for a 1/119 chance (0.88%-0.044%) of not getting COVID, so if you assumed COVID-19 symptoms on average were twice as frequent as vaccine symptoms you were increasing your likelihood of getting ill 60-fold by vaccinating (along with the injection site specific symptoms only seen from the vaccine) in return for a possible halving of COVID symptoms (although in reality, people often felt far worse post-vaccine than during COVID). If you attempted to counterweight that by the major benefits of vaccine, the most important one, death, was not prevented, while the medium one “severe COVID” had required between 2,293 to 6,123 vaccinations to prevent one instance (with the higher figure arising if a consistent metric had been used by Pfizer), and the only other possible justification for vaccinating (reducing transmission) had not been tested in the paper.

Furthermore, since fairly consistent methods are used to doctor papers, I was relatively certain:
•Vaccine efficacy had been overstated (e.g., COVID cases in vaccine recipients were not reported) and severe injuries in vaccine recipients also were not reported—both of which were later corroborated by numerous trial participants and trial researchers.
Note: while the trials were happening (inspired by what I’d learned happened in the Gardasil trials where many of the reported adverse events were magically erased), I joined online support groups for the trial participants and noted that many of the adverse events they reported did not appear in the final trial report, and that the overall severity from a reaction to the vaccine was significantly worse than what I typically saw people experience with COVID-19. My suspicion adverse reactions were covered up in the trial solidified once the vaccine hit the market, because almost immediately, I had multiple patients each day seeking help for severe and unusual vaccine reactions and people I knew from around the country began contacting me to ask if the vaccine could cause strokes or heart attack (as it had happened to someone they knew)—and most importantly, my sample size for these early reports was far smaller than the 18,198 vaccine recipients in the trial.

Any benefits not reported in this paper (e.g., transmission or reducing death) would never be found for this vaccine as every possible attempt had been made to exaggerate the benefits and they could only decline from this point forward (e.g., before long everyone would have immunity to the original strain and COVID-19 would mutate to something no longer covered by the vaccine).
Note: at a six month follow up, deaths were slightly higher in the vaccinated than the unvaccinated group. Likewise, despite there being no evidence that the vaccine prevented transmission (and its symptom-reducing design arguing against this even being possible) health authorities and the media widely promoted the vaccine as preventing transmission to pressure people to vaccinate, until real life data forced them to backtrack on their claim.

•Flipping the criteria for severe COVID-19 (compared to minor COVID) to make the vaccine look better demonstrated that data manipulation was occurring in the paper (hence casting everything else into doubt). Later, as I started noticing a lot of people become severe ill with COVID-19 (and in many cases dying) immediately after vaccinating (including individuals who had minor PCR confirmed asymptomatic infections), I realized this issue had most likely been detected by Pfizer and hence why the criteria for evaluating COVID hospitalizations was changed to “seven days post the second vaccination” (which resulted in many vaccine COVID-19 deaths being labeled as “unvaccinated” deaths).
Note: “disease provocation” due to vaccine-induced immune suppression is a longstanding problem with vaccination (e.g., a good case can be made many of the pre-polio vaccine polio outbreaks were due to vaccination, COVID-19 was the two most common fatal COVID vaccine reactions reported to VAERS and longitudinal data showed the more COVID vaccines you got the more likely you were to get COVID-19)—all of which is discussed here.

Put differently, my immediate thought after looking at the paper was that if after all their best attempts to make the vaccine look as good as possible, it was still this bad, it meant the actual data was likely appalling. Remarkably however, when I discussed this paper my physician colleagues, they could only “see” the 95% effective figure (the 20-fold relative reduction) and all the other points I raised, which were in the paper, went in one ear and out the other, hence illustrating that most people simply do not have a good grab on probabilistic reasoning (outside of those in competitive fields where optimizing EV choices is necessary for success).

Note: the formula which goes hand in hand with EV is Bayes’ theorem [P(A|B) = [P(B|A) × P(A)] / P(B)], which provides a method for updating the probability of something being true as new evidence becomes available. In medicine, it is essential for correctly interpreting diagnostic tests (e.g., understanding that a positive result from a screening test in a low-risk population is more likely to be a false positive than a true one), yet remarkably few physicians actively apply it in their clinical reasoning1,2—which in turn leads to a significant amount of overtesting (some of which in fairness, they know is not justified but is done to avoid potentially being sued), overdiagnosis, and unnecessary treatment.

Finally, it should be noted that the EV of the COVID vaccines was much easier to calculate than that of most other vaccines in use (because there was a much smaller set of variables and much more available data on those variables). For example, to begin calculating the benefit of a routine vaccination, you first need to start with:

Then you need to weigh that against the risks of each vaccine in the series (as later ones typically cause more injuries), with separate calculations done for each degree of injury severity, along with subgroup susceptibility (as some people are much more sensitive to vaccine injury than others) and then once that is done, somehow assess the cumulative effect of all the different vaccines being taken (as vaccine toxicity and immune dysregulation are cumulative). However, rather than try to engage in that complex calculation, the medical industry’s solution has been to assume all vaccines are “magically safe and effective” and like the COVID vaccine, give both incredibly optimistic models of efficacy while only focusing on a few inconsequential reactions (e.g., temporary injection site reactions).

As such, much in the same way doctors were convinced the COVID-19 vaccines would end COVID because it was “95% effective” (when nothing of the sort then happened) and that the vaccine was much safer than getting COVID (despite trial data indicating the opposite), virtually no knowledge exists on the actual EV of most vaccines because they were given a simplified formula to calculate them which only highlights a few key variables industry wants people to focus (which arrive at a high EV). This sales strategy, in turn, is quite effective as it allows people to avoid the hard mental work of having to complete a complex calculation (hence appealing to human laziness), while simultaneously appealing to the human ego by providing the illusion of mastery and authority in the area (by regurgitating the simple arguments used to authoritatively enshrine a positive EV for the vaccines).

Note: a while back I tried to calculate the risks and benefits of each childhood vaccine (as they vary immensely with some being much worse than others)—all of which is detailed here.

Lastly, it should be acknowledged that the original emergency use authorizations for the COVID vaccines were granted under the premise that no other treatment existed, the vaccine’s massive potential benefit justified the existing uncertainty over its effectiveness, and that authorization could be modified as more data emerged. However, not only did other treatments already exist, the FDA then shredded the EV of the vaccines by continually doubling down as more and more evidence of ineffectiveness and harm accumulated.

Stagnating Science

The following holds true for our current society:

•It highly values science and scientific truth to the point that many people worship it in place of religion.

•In order for science to be “valid” (and widely promoted by the media) two bars typically must be cleared—a large randomized control trial is conducted that arrives at a statistically significant corroborating outcome and the scientific authorities must bless a given scientific conclusion.

In some cases, this is a very helpful framework, but in many instances, it is extremely vulnerable to abuse. This is because:

•Large RCTs are extremely expensive (tens of millions of dollars), to the point that they typically can only be financed by national governments, massive pseudo-non profits (e.g., the Gates Foundation), or pharmaceutical companies.

•Any controversial study that somehow makes it through that ideological filter will still often be routinely dismissed by the medical authorities (and in many cases retracted once too many people start citing it).

•Studies that do not meet this threshold are very easy to dismiss, and will virtually always be dismissed if they arrive at a conclusion that threatens a major interest.
Note: it is very common for the abstract or conclusion of a study to provide a summary which contradicts the study’s results if the actual data is “politically incorrect” or “undesirable” (as most people only ever read summaries). Fortunately, AI now makes it very easy to expose this tactic.

•Since most scientists are dependent upon either grants or pharmaceutical funding (the only two sources of funding for costly research), they quickly learn they cannot pursue “controversial research” and hence do not produce research that will tank the rest of their career.

Because of this, we’ve run into a situation where most research is highly conservative and incrementally builds upon existing discoveries rather than making new revolutionary discoveries which advance science and change paradigms. For example, this is how Gerald Pollack aptly described our current situation.

from:  https://www.midwesterndoctor.com/p/the-critical-calculation-medicine?publication_id=748806&post_id=196647596&isFreemail=true&r=19iztd&triedRedirect=true&utm_source=substack&utm_medium=email

ANd Now, A “Sprayable” Covid Vaccine

Sprayable COVID Vaccine Trial Raises ‘Significant Safety Concerns’

Several scientists and researchers questioned the design of the trial for the CVXGA1 nasal vaccine, suggesting the trial did not examine “if shed materials can be spread to others.” The trial also included just 72 participants and lacked an unvaccinated control group.

women getting nasal vaccine

A sprayable intranasal mRNA COVID-19 vaccine demonstrated effectiveness in its Phase 1 clinical trial, according to a study published last week in the journal Science Advances.

However, critics questioned the trial’s design and limited sample size. And some suggested that the sprayable vaccine — CVXGA1, produced by CyanVac LLC — could pose a risk to the public.

Investigative journalist Sonia Elijah noted that CVXGA1, which enters the mucus membranes and lungs through the nose, has the “potential for shedding viral particles through intranasal secretions, which could expose unvaccinated individuals.”

Elijah said the study didn’t examine if shed materials can be spread to others. “This raises significant safety concerns about replication and shedding risks,” she said.

Karl Jablonowski, Ph.D., senior research scientist for Children’s Health Defense, said the platform CVXGA1 uses as a vector is parainfluenza virus type 5, a “communicable respiratory virus between humans and non-human animals that is evading our immune system.”

Jablonowski said this platform exacerbates the risk of shedding. “Since it is self-spreading, there is no informed consent or medical precautions as the ‘vaccine’ may infect infants, children, pregnant women, immunocompromised or medically frail.”

Karina Acevedo Whitehouse, Ph.D., professor of microbiology at the Autonomous University of Querétaro in Mexico, agreed. Citing studies involving similar vaccines, Whitehouse said there are “high chances” this vaccine will result in “persistent shedding.”

Whitehouse cited a 2023 study of an intranasal RSV (respiratory syncytial virus) vaccine, which detected virus shedding in 17% of participants.

CVXGA1 produces the SARS-CoV-2 virus spike protein — which was also contained in the mRNA COVID-19 vaccines produced by Pfizer and Moderna.

Medical experts and peer-reviewed studies have suggested the spike protein poses potentially serious risks to human health.

“Genetically modifying an infectious respiratory virus to express a spike protein is a familiar and really bad idea,” Jablonowski said. “The immune system will be antagonized by the presence of the spike protein.”

Clinical trial flawed, experts say

According to the CVXGA1 Phase 1 study, CVXGA1 “is a potentially effective intranasal COVID-19 vaccine” that produces an immune response with minimal adverse reactions.

The clinical trial included just 72 participants, ages 12-53, split into two groups. One group received a “high dose” of the vaccine, the other received a smaller dose.

Findings showed the high-dose group demonstrated “Significantly lower rates of symptomatic COVID-19 infection” and that the vaccine was “well tolerated without serious adverse events (AEs) or fever reported.”

However, several scientists and researchers noted that the trial lacked an unvaccinated control group.

“There is absolutely no way that this paper can be considered evidence that this intranasal gene-therapy based product is safe or effective,” Whitehouse said. “No group was used as a control with which to compare the results … as well as adverse events. This in itself invalidates any interpretation of safety and effectiveness of this product.”

According to Elijah, the lack of a control group and the small sample size “weakens the trial’s ability to accurately assess safety and immunogenicity,” but these aren’t the only flaws.

Elijah said:

“The study lacks data on RNA detection levels and did not perform infectivity assays to confirm if shed materials can be spread to others.

“The lack of specific safety and immunogenicity data for the adolescent group raises concerns about the vaccine’s effects in younger individuals.

“The open-label design, where both participants and researchers knew who received the vaccine, introduces potential bias in reporting and assessing outcomes, such as adverse events.”

Whitehouse noted that the study’s researchers claimed they didn’t identify any serious adverse events. However, they tracked adverse events only “during a limited time frame,” which “reduces the chances of detecting serious events that may occur after this time period.”

Researchers plan to enroll 10,000 participants for the next phase of the clinical trial.

According to immunologist and biochemist Jessica Rose, Ph.D., if clinical trials for CVXGA1 are deemed a success, “this could be used to push gene-based (mRNA, RNA and DNA) products on us via intranasal (breathing) routes.”

Clinical trial site previously hosted Pfizer COVID vaccine trials for adolescents

Experts also noted that the clinical trials were not performed independently but were fully funded by CyanVac.

According to the study’s disclosure statement, several of the researchers are CyanVac employees or equity holders, are under contract with the company, or have received research grants from other pharmaceutical companies, including COVID-19 vaccine manufacturers AstraZeneca, Moderna and Pfizer.

Investors such as Bill Gates have previously shown interest in inhalable and sprayable vaccines, although it is unclear whether Gates is involved with the development of CVXGA1.

Elijah noted that Cincinnati Children’s Hospital ran the trial and Dr. Paul Spearman, the hospital’s vice chair of clinical and translational research and education, led it. The hospital was one of the sites for adolescent clinical trials of Pfizer’s COVID-19 vaccine.

In 2021, a participant in one of those trials, 12-year-old Maddie de Garay, was severely injured after she received the second dose of the Pfizer vaccine. She sustained several serious adverse events and ended up in a wheelchair.

According to Elijah, doctors at the hospital dismissed any connection between de Garay’s injuries and the Pfizer vaccine, and instead classified her injuries as “neuralgia and functional abdominal pain.”

from:  https://childrenshealthdefense.org/defender/sprayable-covid-vaccine-trial-raises-safety-concerns/

What’s “Living” in Your Body?

New Study from Japan: Covid Shots Installed Nanobots

A new Japanese study shows that Pfizer and Moderna vaccines contain unauthorized “animated worm-like” entities, invisible to the human eye, which swim, wiggle, and assemble themselves into complex structures, which cause clots inside the body. Researchers Dr. Young Mi Lee and Dr. Daniel Broudy isolated unused Pfizer and Moderna vaccine vials for 3 weeks, and then examined them under 400X magnification. They noticed that when the nano-technology was energized, it created “discs, chains, spirals, tubes, and right-angle structures.” The scientists believe these mysterious nanoparticles are responsible for the explosion of “turbo cancer” and autoimmune diseases around the globe. They also concluded that humans into controllable “Biohybrid Magnetic Robots.” The suggested that the smart microscopic components are part of the elite’s “long-planned well-funded Internet of Bodies,” which was described as a kind of “synthetic global central nervous system” turning humans into controllable “Biohybrid Magnetic Robots.” The researchers called for a ban on mRNA shots. They also demanded the labels “vaccine” and “safe and effective” be removed because the substances are not vaccines and they are dangerous..

Link for Study:   Real-Time Self-Assembly of Stereomicroscopically Visible Artificial Constructions in Incubated Specimens of mRNA Products Mainly from Pfizer and Moderna: A Comprehensive Longitudinal Study

From Seemorerocks:

Another Confirmation Of Self Assembly Nanotechnology In COVID Bioweapons: Remarkable Longitudinal Study And Culture Work Of COVID Shots For Up To 12 Months And Cellular Toxicity Studies

New Japanese study proves Pfizer and Moderna v*ccines contain unauthorized “animated worm-like” entities, invisible to the human eye, which swim, wiggle, and assemble themselves into complex structures, which cause clots inside the body. (What embalmer Richard Hirschman found and exposed in the film Died Suddenly).

Dr. Young Mi Lee and Dr. Daniel Broudy from Okinawa Christian University discovered these “undisclosed additional engineered components” by isolating unused vaxx vials for 3 weeks, and then examined them under 400X magnification.

Lee and Broudy saw that when the nanotechnology was energized it created “discs, chains, spirals, tubes, and right-angle structures.”

The researchers, who published their findings in the International Journal of Vaccine Theory Practice and Research, believe these mysterious nanoparticles are responsible for the explosion of “turbo cancer” and autoimmune diseases around the globe.

They also concluded in the study their suspicion that these smart microscopic components are part of the elite’s “long-planned well-funded Internet of Bodies,” which was described as a kind of “synthetic global central nervous system” turning humans into controllable “Biohybrid Magnetic Robots.”

The study ends by calling for a global ban on all mRNA shots, until these nanobots are studied long-term. They also demanded the labels “v*ccine” and “safe and effective” be removed because the concoction injected into billions is officially neither.

Another Confirmation Of Self Assembly Nanotechnology In COVID Bioweapons: Remarkable Longitudinal Study And Culture Work Of COVID Shots For Up To 12 Months And Cellular Toxicity Studies

In this important study, Dr Young Mi Lee with Dr Daniel Broudy describes her culture findings of Pfizer and Moderna Bioweapons. Many different studies were done, including incubation of the COVID injections, cellular effects upon blood and semen specimen. The tests showed direct toxicity to semen and death of all sperm within minutes up to 1.5 hours in the healthiest donor samples when put in contact with the “vaccine” solution. EMF exposure was also tested, in addition with different supplements and treatment solutions. For this substack, select images were taken from the article which is 66 pages long. Please refer to this link and download the paper – please share widely – this is one the most comprehensive and long term study of the COVID injections and their cellular effects to date. The findings are entirely consistent with all prior research findings of self assembly nanotechnology from the injectables.

Real-Time Self-Assembly of Stereomicroscopically Visible Artificial Constructions in Incubated Specimens of mRNA Products Mainly from Pfizer and Moderna: A Comprehensive Longitudinal Study

Abstract

Observable real-time injuries at the cellular level in recipients of the “safe and effective” COVID-19 injectables are documented here for the first time with the presentation of a comprehensive description and analysis of observed phenomena. The global administration of these often-mandated products from late 2020 triggered a plethora of independent research studies of the modified RNA injectable gene therapies, most notably those manufactured by Pfizer and Moderna. Analyses reported here consist of precise laboratory “bench science” aiming to understand why serious debilitating, prolonged injuries (and many deaths) occurred increasingly without any measurable protective effect from the aggressively, marketed products. The contents of COVID-19 injectables were examined under a stereomicroscope at up to 400X magnification. Carefully preserved specimens were cultured in a range of distinct media to observe immediate and long-term cause-and-effect relationships between the injectables and living cells under carefully controlled conditions. From such research, reasonable inferences can be drawn about observed injuries worldwide that have occurred since the injectables were pressed upon billions of individuals. In addition to cellular toxicity, our findings reveal numerous — on the order of 3~4 x 106 per milliliter of the injectable — visible artificial self-assembling entities ranging from about 1 to 100 µm, or greater, of many different shapes. There were animated worm-like entities, discs, chains, spirals, tubes, right-angle structures containing other artificial entities within them, and so forth. All these are exceedingly beyond any expected and acceptable levels of contamination of the COVID-19 injectables, and incubation studies revealed the progressive self-assembly of many artifactual structures. As time progressed during incubation, simple one- and two-dimensional structures over two or three weeks became more complex in shape and size developing into stereoscopically visible entities in three-dimensions. They resembled carbon nanotube filaments, ribbons, and tapes, some appearing as transparent, thin, flat membranes, and others as three-dimensional spirals, and beaded chains. Some of these seemed to appear and then disappear over time. Our observations suggest the presence of some kind of nanotechnology in the COVID-19 injectables.

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Figure 5. Direct microscopic findings observed in two dimensions magnified 400X: (a) Remnants and new Pfizer injectables, directly observed as well as after incubation for 1 -2 days. (b) Moderna and 4 dried COVID-19 injectables (Pfizer, Moderna, AstraZeneca, and Novavax).

Figure 6. Interactions observed for whole blood(a)/plasma(b) with Novavax at 400X magnification: (a) Within 1 hour, blood cells formed a prominent barrier against “vaccine” contents. (b) After 30 minutes, severe aggregates of red blood cells in rouleaux appeared in the plasma specimen.

Figure 7. Plasma reactions after two hours with four COVID-19 injectables — Pfizer, Moderna, Novavax, and AstraZeneca: (a) Pfizer showing cellular collapse (pyknosis) of white blood cells and damaged platelets; (b) Moderna with stacks of red blood cells (rouleaux); (c) Novavax with the nucleus of white blood cells disintegrating (karyorrhexis), abnormal platelet aggregations, and some rouleaux of red blood cells; and (d) AstraZeneca with prominent Rouleau of red blood cells.

Figure 8. Reaction of semen to COVID-19 injectables at 200X magnification: (a) semen with normal saline as a control added after two hours; (b) with flu vaccine added as a control after 1.5 hours showed sperm cells with intact morphology and with typical progressive natural reduction in sperm motility; (c) 30 minutes after Pfizer-1 injectable was added, sperm motility showed rapid reduction; (d) Pfizer-1 after one hour, all sperm motility ceased;

(e) 30 minutes after Moderna. injectable added; (f) one hour after Moderna was added sperm cells were completely immotile; (g) 30 minutes after Novavax was added; (h) one hour after Novavax, all motility ceased.

Figure 11. Findings for Pfizer incubation study for 372 days; (a) Day 22, this is what we describe as a beaded chain (at 400X magnification); (b) Day 24, 2- dimensional geometric self-assembly at the bottom (at 200X magnification) in normal saline; (c) Day 60, floating 3-dimensional detailed chip-like structures (at 400X magnification) in distilled water; (d) and (e) day 60, accumulated 3-dimensional chip-like structures within an oval shaped boundary (200X/400X) in distilled water; (f), (g), (h), (i) Floating filaments shedding bubbles inside and outside in normal solution at day 95 (100x/100x/200x/200x); (j), (k), (l), (m) Progressive degenerative changes in distilled water 200X (day 82/day 256/day 306/day 372).

 

Read full article from Seemorerocks at Substack

Warning:  Video contains graphic blood clot extraction.

Click for video link

Click for video transcript

from:    https://needtoknow.news/2024/08/new-study-from-japan-covid-shots-installed-nanobots/

The Pfizer-Spider Web is Growing

Pfizer’s New Heart Pandemic

Is Accountability Coming?

___________________________________________________________________
Originally posted on The Tenpenny Report by Fed Up Texas Chick; Updated by Dr. Sherri Tenpenny

For years, we’ve been writing about how evil Pfizer is. Case in point: this article from 2017 where we featured Dr. Peter Rost, a former vice president of Pfizer and a pharmaceutical industry whistleblower. He is the author of The Whistleblower, Confessions of a Healthcare Hitman, and at the time was talking about how deadly the HPV vaccine was. Dr. Rost claimed that pharmaceutical companies intentionally design vaccines to keep the public in a state of illness for purposes of perpetual treatments.

That was seven years ago, and never has the evil of Pfizer been more apparent. In January 2024, the powers-that-be declared that the new coronavirus variant would likely cause a higher risk of heart problems.

This time, they presented research from RIKEN, Japan’s largest scientific institute, funded nearly entirely by the Japanese government. However, Riken also accepts “donations from individuals and corporations for the enhancement and development of research.” They even have a page where donors can send a direct credit card donation.

I’m sure that is all above board. In 2019, RIKEN had a budget of $900 million, yet they still needed credit card donations?

What types of corporations work with RIKEN? Corporations like Bayer work with RIKEN, like in the drug discovery collaboration they’ve been jointly working on for about five years.

In December 2021, Pfizer announced they would buy Arena Pharmaceuticals. Pfizer had its eye on etrasimod, Arena’s drug for ulcerative colitis. The drug was approved by the FDA in October 2023, and Pfizer now markets it as VELSIPITY™. Pfizer’s website says in the press release that “UC is a chronic and often debilitating condition that affects an estimated 1.25 million people in the United States.”

That’s a lot of people, but is it enough of a market to drive Pfizer to buy Arena at a 100% premium, a $6.7 billion cash deal? That doesn’t add up in my book. Pfizer sped the development of etrasimod because the drug is a potential therapy for all kinds of immuno-inflammatory diseases, including inflammation of the heart. Part of the deal was that Pfizer acquired all Arena assets in gastroenterology, dermatology, and cardiology.

The first links between the COVID-19 mRNA jabs and myocarditis began to be reported in July 2021. In December 2021, Pfizer entered into a formal agreement to purchase Arena, and by March 2022, it was a done deal.

Incredibly, myocarditis incidents began skyrocketing shortly thereafter. In one example from a May 2022 article, emergency cardiac arrest calls for young adults strongly correlated with the vaccine rollout of doses 1 and 2 in Israel, one of the most jabbed countries in the world.

An FDA-sponsored study looked at health records of children from December 2020 to June 2022 and found incidences of myocarditis and pericarditis to be high enough to trigger a safety signal in 12- to 17-year-olds. The timeframe from the jab to seeking cardiac care for myocarditis or pericarditis was 6.8 days. In a literature review from 2020 to 2022, males were approximately seven times more likely than females to present myocarditis/pericarditis. Another recent study concluded that a booster dose is associated with increased myocarditis risk in adolescents and young adults.

Cancer

In early 2023, Pfizer announced another huge deal with purchase of Seagen Pharmaceuticals.

Seagen is known for its pipeline of cancer drugs, and Pfizer really wanted that pipeline because they spent $43 billion on the deal. Pfizer Chairman and CEO Albert Bourla described it as “acquiring the goose that is laying the golden eggs.”

Once again, the purchase begs the question: Is this business prowess on the part of Pfizer, or is it all planned?

The concept of “turbo cancer” was introduced in January 2023 when fact-checkers across the internet began reporting that any connection between the mRNA jabs and turbo cancer was false. By summer, physicians started describing turbo cancers as the new pandemic, and scientists started to provide reasoning for the sudden and aggressive cancers that oncologists were witnessing.

They seemed to start after a COVID-19 booster shot in all cases. Soon, articles like this one were commonplace, with physicians professing they had never seen cancers with this form of aggression who were often dead within a few months, weeks, or sometimes, even days.

Bourla himself said that the world is experiencing a new type of cancer epidemic, which may explain the Seagen purchase. Seagen works with antibody-drug conjugate (ADC) technology, which uses monoclonal antibodies made to seek out cancer cells and deliver a drug to those cells while sparing the surrounding tissue. Bourla called the ADC technology “one of the greatest technologies to battle cancer” and said they were “very much like the mRNA for vaccines.”

Interestingly, Pfizer created the first ADC, Mylotarg, but had to remove it from the market in 2010 after studies showed the drug was more toxic than chemotherapy.

Bourla said the Seagen acquisition will “dramatically change the oncology presence of Pfizer, making it one of a kind. Seagen’s cancer therapy will bring cancer treatment to the world at a scale that has not been seen before.”

Problem. Reaction. Solution.

Unadulterated Greed

Pfizer was literally flooded with cash after 2021.

Pfizer’s revenues in 2021 were double their revenues from 2020 ($81.3 billion). In 2022, they bought Biohaven Pharmaceuticals for $11.6 billion to gain access to the company’s migraine drug. That same year, they also purchased Global Blood Therapeutics to gain access to the company’s sickle cell drug Oxbryta. But only approximately 100,000 Americans suffer from sickle cell; how can they make $3 billion off this drug? What does Pfizer know that the rest of us don’t? Will we see a blood cell disease epidemic as well?

Some analysts note that, ultimately, Pfizer may go bankrupt with all the lawsuits on the horizon. Will Pfizer go the way of Purdue Pharma, a company where greed and dishonesty allowed it to continue marketing harmful products to the public? Just as with Purdue, will Pfizer lose its legal protections when the millions of vaccine injury claims and charges of fraud land on Bourla’s desk?

The days of huge revenues from COVID-19 products have passed. The US government is returning $3.5 billion of unused Paxlovid treatments, and Pfizer is facing revenue losses from many patent expirations and unfulfilled government contracts worldwide.

Vigilant News noted that older, more experienced vaccine companies such as GSK did not enter the COVID-19 vaccine fray. That looks like it was a wise choice. However, they no doubt got paid well for sitting this one out.

Today, Pfizer’s stock is far less valuable than it was just a few years ago, despite the flashy acquisitions of companies like Arena and Seagen and the billions of dollars made from the COVID death jabs. In the last year, Pfizer has underperformed by 35% compared to the overall pharmaceuticals index.

We can only hope Pfizer – and all other players such as doctors, nurses, pharmacists, politicians, and governments will have soon pay dearly for their folly. That is the heart of the matter.

from:    https://drtenpenny.substack.com/p/pfizers-new-heart-pandemic?publication_id=931759&post_id=145808579&isFreemail=true&r=19iztd&triedRedirect=true&utm_source=substack&utm_medium=email

Shedding a Light on Covid Vaccine Shedding

COVID Vaccine Shedding Is ‘Real’, FDA & Pfizer Documents Are Proof: Clinicians

BY TYLER DURDEN
MONDAY, FEB 19, 2024 – 10:05 AM

Authored by Marina Zhang via The Epoch Times (emphasis ours),

The topic of COVID-19 vaccine shedding has long been controversial, but now, some doctors say it is real.

(myboys.me, Naeblys/Shutterstock)

Shedding is unfortunately real,” said Dr. Pierre Kory at the Front Line COVID-19 Critical Care Alliance (FLCCC) conference in Phoenix, Arizona, in early February. “The FDA (U.S. Food and Drug Administration) knows that.”

Dr. Kory is a co-founder of the FLCCC, a non-profit advocacy group founded by physicians for the treatment of COVID-19, long COVID, and postvaccine syndromes. He is also the co-founder of the Leading Edge Clinic and has treated over a thousand long-COVID and postvaccine patients.

Fact-checkers have largely denied shedding on the basis of definition. The commonly cited definition comes from the U.S. Centers for Disease Control and Prevention (CDC) website, which defines shedding as the release of viruses, bacteria, and their components from live vaccines.

While mRNA and adenovirus vaccines are not live vaccines, they function similarly to gene therapy products.

All gene therapy products pose a risk of shedding, according to the FDA.

FDA Documents

In a 2015 document titled Design and Analysis of Shedding Studies for Virus or Bacteria-Based Gene Therapy and Oncolytic Products, the FDA defines shedding as “the release of [viral or bacterial gene therapy products] … from the patient through one or all of the following ways: excreta (feces); secreta (urine, saliva, nasopharyngeal fluids etc.); or through the skin (pustules, sores, wounds).”

In the same document, the FDA also explains what gene therapy products are: “All products that mediate their effects by transcription and/or translation of transferred genetic material.”

The COVID-19 mRNA and adenovirus vaccines fall into this category. They mediate their effects by inducing the body to translate mRNA genetic information into spike proteins.

Some gene therapy products known to shed include an eye treatment branded as Luxturna. Luxturna uses an adenovirus carrier to deliver eye protein DNA to retina cells in patients.

The Luxturna adenovirus and its DNA have been found in patients’ tears, according to the product’s package insert.

Similarly, mRNA and adenovirus COVID-19 vaccines may cause vaccinated patients to release spike proteins or other vaccine components, Dr. Kory explained.

For example, COVID-19 mRNA has been found in the breast milk of vaccinated mothers, indicating possible exposure of the vaccine to infants. Another study showed that spike protein, the product of COVID-19 vaccination, can last for at least half a year in the blood of vaccinated individuals, indicating prolonged spike protein persistence.

The FDA, however, denied that the 2015 document applies to COVID mRNA vaccines.

“COVID-19 vaccines are not regulated as gene therapy products by the FDA; therefore, the guidance document cited is not applicable to the COVID-19 vaccines,” an FDA spokeswoman told The Epoch Times.

Pfizer Investigators Told to Report ‘Environmental’ Vaccine Exposures

Another piece of evidence resides in Pfizer documents, Dr. Kory added.

In Pfizer’s COVID mRNA vaccine protocol, the company instructs investigators to report “environmental exposures” if trial participants expose people around them to the vaccine through inhalation or skin contact.

Examples of such environmental exposures are noted as follows:

  • A male participant who is receiving or has discontinued [vaccine] intervention exposes a female partner prior to or around the time of conception.”
  • “A female family member or healthcare provider reports that she is pregnant after having been exposed to the [vaccine] intervention through inhalation or skin contact.”

The protocol also goes into what Dr. Kory and his clinic co-founder, Scott Marsland, call “secondary shedding.” This occurs when a person who has had environmental exposure to the vaccine then exposes another person.

An example of environmental exposure during breastfeeding,” Pfizer writes, “is a female family member or healthcare provider who reports that she is breastfeeding after having been exposed to the study intervention (the vaccine) by inhalation or skin contact.”

Pfizer’s Documents Showing Indirect Exposures

Pfizer has documented hundreds of adverse events that occurred as a result of indirect exposures or exposure to babies during pregnancy or breastfeeding.

In its Periodic Safety Report submitted to the European Union, Pfizer listed several adverse events it deemed not attributable to the vaccine and that should be excluded from discussion.

The document listed 22 cases of adverse events in babies who had received “indirect exposure” to COVID mRNA boosters, suggesting exposure other than a direct vaccination.

The investigators also monitored several special adverse event cases. Two blood-related adverse events involved babies being exposed through breastfeeding. Ten cases of liver-related adverse events and one adverse event of the vasculature system were reported for the same reason.

Two cases of acute kidney or renal failure and eight respiratory cases also involved babies being exposed during pregnancy or breastfeeding.

Testimonies From Patients

Patients who may be affected by vaccine exposure tend to be those with a history of sensitivities and chronic diseases, said Dr. Kory and Mr. Marsland. They also tend to have bad experiences with pharmaceuticals and are more likely to be chronically debilitated by COVID-19 or the vaccine.

Dr. Kory said that after compiling over 800 anecdotal reports, they observed a clear pattern in symptoms that they determined to be shedding.

Typically, the manifestation of symptoms is repeatable and predictable, such as when a person repeatedly becomes symptomatic when going into supermarkets or crowded places.

Dr. Kory gave the example of a patient who noticed he could not handle going into grocery stores.

The patient told Dr. Kory that he just couldn’t “go into grocery stores anymore.” Within five minutes of entering a Trader Joe’s grocery store, he “feels so terrible” that he has to leave. He experienced the same aversion upon going to a crowded farmers market.

At the FLCCC event, Mr. Marsland also shared several cases where he believed shedding was involved.

One case involved a 54-year-old male, who previously suffered from symptoms after the COVID-19 vaccine, meeting up with a friend who received a COVID-19 booster.

They sat close to each other, talking and laughing. “Within hours of spending their time together, [the man] had a headache, myalgia, and joint pain, increased fatigue,” Mr. Marsland relayed.

When the patient went to a busy airport, he felt worse.

He returned home and had sexual contact with his spouse, exchanging bodily fluids. Within minutes, the spouse developed severe “nine out of 10” abdominal pain.

The two believed the pain was from shedding, so both took ivermectin, known to bind to and block spike proteins. Within about half an hour, the spouse’s abdominal pain receded.

“It’s the temporal association and the accumulation of symptoms,” Mr. Marsland reasoned.

Other doctors treating long COVID and postvaccine syndromes, such as Dr. Syed Haider and Dr. Ana Mihalcea, have also reported suspected cases of shedding.

Some Vaccinologists Disagree

Professors in vaccinology, however, do not acknowledge that mRNA vaccines may induce shedding.

“mRNA leads to the expression of proteins in cells, and this expression is different from shedding, as you would have if you are infected by certain viruses,” associate professor Paulo Verardi of the University of Connecticut told The Epoch Times.

While SARS-CoV-2 infection leads to virus shedding, and, therefore, transmission of the virus from person to person, shedding of the spike protein does not occur in individuals receiving the COVID-19 mRNA vaccine,” he continued.

While another definition of shedding refers to the release of live viruses in people infected or vaccinated with live vaccines, Dr. Kory reiterated that the shedding discussed in the case of COVID-19 vaccines is different from the shedding of live viruses.

Professor Florian Krammer at the Icahn School of Medicine at Mount Sinai also told The Epoch Times that shedding does not exist.

He did not reply when The Epoch Times presented him with information regarding the FDA’s documents on gene therapy and shedding.

from:    https://www.zerohedge.com/political/covid-vaccine-shedding-real-fda-and-pfizer-documents-are-proof-clinicians?utm_source=&utm_medium=email&utm_campaign=2287

Who is “THE SCIENCE”?

And The Truth of the Matter…

Researcher Naomi Wolf Says Babies Were Murdered by Pfizer Shots

The Department of Health and Human Services (HHS) was paying OB-GYN doctors millions of dollars to lie to mothers that COVID mRNA injections are safe. Naomi Wolf said that if the doctors tell the truth about the dangers of COVID injections, they will have to repay the money that they received. She said that they are criminals. She said that Pfizer is aware that babies died after their mothers received COVID jabs. She asserted that babies and unborn babies have been murdered.

CHECK IT OUT HERE:

Link for video:         https://www.bitchute.com/video/TyU52rcerJyi/

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Summary by JW WIlliams

Naomi Wolf, a researcher and the CEO of Daily Clout, said that the Department of Health and Human Services (HHS) was paying OB-GYN doctors millions of dollars to ‘stick to the script’ and to lie to mothers that COVID mRNA injections are safe. She said that if the doctors tell the truth about the dangers of COVID injections, they will have to repay the money that they received. Wolf called these doctors criminals.

She said that the American College of Obstetrics and Gynecology, a large lobbying group, had a portal where OB-GYN doctors could register to receive money directly fro HHS in 2020 if they attested that their patients had COVID as a primary diagnosis, or, if they were pregnant, COVID could be used as a secondary diagnosis. OB-GYN doctors were incentivized in 2020 to inflate COVID diagnosis numbers.

Wolf reported that maternal deaths are up 40% after COVID injections. She said that a doctor and midwives have told her that babies are being born prematurely, they are being born with fetal malformations, chromosomal malformations and breathing problems.

She said that babies and unborn have been murdered.

Wolf said that Pfizer documents reveal that they knew that two babies died in-utero and the vaccine manufacturer stated that the deaths were due to “trans-placental exposure” to the vaccine and then they sent that report to the CDC in April 10, 2021. Three days later, CDC head Rochelle Walensky gave a press conference from the White House stating that pregnant women should take the mRNA vaccines and that it was safe and effective at any time, before, during, or after pregnancy. Wolf said that Walensky knew that two babies had died from trans-placental exposure and another baby died from poisoned breast milk when she advised the women to take the COVID shots.

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Gateway Pundit:         https://www.thegatewaypundit.com/2023/08/must-see-video-naomi-wolf-we-know-pfizer/

from:    chttps://needtoknow.news/2023/08/researcher-naomi-wolf-says-babies-were-murdered-by-pfizer-shots/

Turing the Tide on mRNA Vaccine Administers

New Idaho Bill to Charge Those Who Administer mRNA Vaccines with Misdemeanor

A new bill has been introduced in Idaho that would make the administration of experimental mRNA COVID-19 vaccines illegal.

Representative Judy Boyle (R-Midvale) and Senator Tammy Nichols (R-Middleton) sponsored House Bill 154.

Sen. Nichols introduced the new bill on the 15th of February before the House Health and Welfare Committee, according to KTVB.

According to the bill text, “A person may not provide or administer a vaccine developed using messenger ribonucleic acid technology for use in an individual or any other mammal in this state.”

A person who violates the bill will be guilty of a misdemeanor.

The new legislation, if passed, would go into effect on July 1, 2023.

KTVB reported:

Nichols said during her presentation to the committee, “We have issues this was fast tracked.”

Nichols said there is no liability, informed consent or data on mRNA vaccines. She later clarified she was referring to the two COVID-19 vaccines, Pfizer and Moderna.

“I think there is a lot of information that comes out with concerns to blood clots and heart issues,” Nichols said.

Rep. Ilana Rubel, D-Boise, questioned Nichols’ statement that the vaccines were fast-tracked. She said her understanding was that the vaccines were approved and survived the testing, later approved by the FDA.

Nichols said she is finding it “may not have been done like we thought it should’ve been done.”

“There are other shots we could utilize that don’t have mRNA in it,” Nichols said.

More and more medical experts, scientists, and right group advocates all over the world are now demanding that the government should stop its COVID-19 vaccination campaign due to its devastating side effects among patients.

And yet governments still turn a blind eye to one of the most atrocious crimes against humanity.

from:    https://www.thegatewaypundit.com/2023/02/new-idaho-bill-charge-administer-mrna-vaccines-misdemeanor/

SO Here is Profitability Guarantee a la Pfizer

pfizer new thumb 2023

Pfizer Executive: ‘Mutate’ COVID via ‘Directed Evolution’ for Company to Continue Profiting Off of Vaccines … ‘COVID is Going to be a Cash Cow for Us’ … ‘That is Not What We Say to the Public’ … ‘People Won’t Like That’ … ‘Don’t Tell Anyone’

  • Jordon Trishton Walker, Pfizer Director of Research and Development, Strategic Operations – mRNA Scientific Planner: “One of the things we’re exploring is like, why don’t we just mutate it [COVID] ourselves so we could create — preemptively develop new vaccines, right? So, we have to do that. If we’re gonna do that though, there’s a risk of like, as you could imagine — no one wants to be having a pharma company mutating f**king viruses.”
  • Walker: “Don’t tell anyone. Promise you won’t tell anyone. The way it [the experiment] would work is that we put the virus in monkeys, and we successively cause them to keep infecting each other, and we collect serial samples from them.”
  • Walker: “You have to be very controlled to make sure that this virus [COVID] that you mutate doesn’t create something that just goes everywhere. Which, I suspect, is the way that the virus started in Wuhan, to be honest. It makes no sense that this virus popped out of nowhere. It’s bullsh*t.”
  • Walker: “From what I’ve heard is they [Pfizer scientists] are optimizing it [COVID mutation process], but they’re going slow because everyone is very cautious — obviously they don’t want to accelerate it too much. I think they are also just trying to do it as an exploratory thing because you obviously don’t want to advertise that you are figuring out future mutations.”

[NEW YORK – Jan. 25, 2023] Project Veritas released a new video today exposing a Pfizer executive, Jordon Trishton Walker, who claims that his company is exploring a way to “mutate” COVID via “Directed Evolution” to preempt the development of future vaccines.

Walker says that Directed Evolution is different than Gain-of-Function, which is defined as “a mutation that confers new or enhanced activity on a protein.” In other words, it means that a virus such as COVID can become more potent depending on the mutation / scientific experiment performed on it.

The Pfizer executive told a Veritas journalist about his company’s plan for COVID vaccines, while acknowledging that people would not like this information if it went public.

“One of the things we [Pfizer] are exploring is like, why don’t we just mutate it [COVID] ourselves so we could create — preemptively develop new vaccines, right? So, we have to do that. If we’re gonna do that though, there’s a risk of like, as you could imagine — no one wants to be having a pharma company mutating f**king viruses,” Walker said.

“From what I’ve heard is they [Pfizer scientists] are optimizing it [COVID mutation process], but they’re going slow because everyone is very cautious — obviously they don’t want to accelerate it too much. I think they are also just trying to do it as an exploratory thing because you obviously don’t want to advertise that you are figuring out future mutations,” he said.

“Don’t tell anyone. Promise you won’t tell anyone. The way it [the experiment] would work is that we put the virus in monkeys, and we successively cause them to keep infecting each other, and we collect serial samples from them.”

Walker drew parallels between this current Pfizer project and what may have happened at the Wuhan Institute of Virology in China.

“You have to be very controlled to make sure that this virus [COVID] that you mutate doesn’t create something that just goes everywhere. Which, I suspect, is the way that the virus started in Wuhan, to be honest. It makes no sense that this virus popped out of nowhere. It’s bullsh*t,” he said.

“You’re not supposed to do Gain-of-Function research with viruses. Regularly not. We can do these selected structure mutations to make them more potent. There is research ongoing about that. I don’t know how that is going to work. There better not be any more outbreaks because Jesus Christ,” he said.

Walker also told the Veritas journalist that COVID has been instrumental for Pfizer’s recent business success:

Walker:Part of what they [Pfizer scientists] want to do is, to some extent, to try to figure out, you know, how there are all these new strains and variants that just pop up. So, it’s like trying to catch them before they pop up and we can develop a vaccine prophylactically, like, for new variants. So, that’s why they like, do it controlled in a lab, where they say this is a new epitope, and so if it comes out later on in the public, we already have a vaccine working.

Veritas Journalist:Oh my God. That’s perfect. Isn’t that the best business model though? Just control nature before nature even happens itself? Right?

Walker:Yeah. If it works.

Veritas Journalist:What do you mean if it works?

Walker:Because some of the times there are mutations that pop up that we are not prepared for. Like with Delta and Omicron. And things like that. Who knows? Either way, it’s going to be a cash cow. COVID is going to be a cash cow for us for a while going forward. Like obviously.

Veritas Journalist:Well, I think the whole research of the viruses and mutating it, like, would be the ultimate cash cow.

Walker:Yeah, it’d be perfect.

Walker went on to explain how Big Pharma and government officials, such as at the Food & Drug Administration [FDA], have mutual interests, and how that is not in the best interest of the American people:

Walker:[Big Pharma] is a revolving door for all government officials.

Veritas Journalist:Wow.

Walker:In any industry though. So, in the pharma industry, all the people who review our drugs — eventually most of them will come work for pharma companies. And in the military, defense government officials eventually work for defense companies afterwards.

Veritas Journalist:How do you feel about that revolving door?

Walker:It’s pretty good for the industry to be honest. It’s bad for everybody else in America.

Veritas Journalist:Why is it bad for everybody else?

Walker:Because when the regulators reviewing our drugs know that once they stop regulating, they are going to work for the company, they are not going to be as hard towards the company that’s going to give them a job.

About Project Veritas

James O’Keefe established Project Veritas in 2010 as a non-profit journalism enterprise to continue his undercover reporting work. Today, Project Veritas investigates and exposes corruption, dishonesty, self-dealing, waste, fraud, and other misconduct in both public and private institutions to achieve a more ethical and transparent society and to engage in litigation to: protect, defend and expand human and civil rights secured by law, specifically First Amendment rights including promoting the free exchange of ideas in a digital world; combat and defeat censorship of any ideology; promote truthful reporting; and defend freedom of speech and association issues including the right to anonymity. O’Keefe serves as the CEO and Chairman of the Board so that he can continue to lead and teach his fellow journalists, as well as protect and nurture the Project Veritas culture.

Project Veritas is a registered 501(c)3 organization. Project Veritas does not advocate specific resolutions to the issues raised through its investigations.

from:    https://www.projectveritas.com/news/pfizer-executive-mutate-covid-via-directed-evolution-for-company-to-continue/

Pfizer Told 8 Months to Release “Vaccine” Data

Judge Rejects FDA’s 75 Year Delay On Vax Data, Cuts To Just 8 Months

by Tyler Durden
Friday, Jan 07, 2022 – 06:11 AM

A federal judge has rejected a request by the FDA to produce just 500 pages per month of the data submitted by Pfizer to license its Covid-19 vaccine – and has ordered them to produce 55,000 pages per month. Assuming there are roughly 450,000 pages, that means it will take just over eight months for the world to see what’s under the hood.

Attorney Aaron Siri, who represents the plaintiff in the case, has provided this stunning update via his blog, Injecting Freedom:

On behalf of a client, my firm requested that the FDA produce all the data submitted by Pfizer to license its Covid-19 vaccine.  The FDA asked the Court for permission to only be required to produce at a rate of 500 pages per month, which would have taken over 75 years to produce all the documents.

I am pleased to report that a federal judge soundly rejected the FDA’s request and ordered the FDA to produce all the data at a clip of 55,000 pages per month!

This is a great win for transparency and removes one of the strangleholds federal “health” authorities have had on the data needed for independent scientists to offer solutions and address serious issues with the current vaccine program – issues which include waning immunity, variants evading vaccine immunity, and, as the CDC has confirmed, that the vaccines do not prevent transmission.

No person should ever be coerced to engage in an unwanted medical procedure.  And while it is bad enough the government violated this basic liberty right by mandating the Covid-19 vaccine, the government also wanted to hide the data by waiting to fully produce what it relied upon to license this product until almost every American alive today is dead.  That form of governance is destructive to liberty and antithetical to the openness required in a democratic society.

In ordering the release of the documents in a timely manner, the Judge recognized that the release of this data is of paramount public importance and should be one of the FDA’s highest priorities.  He then aptly quoted James Madison as saying a “popular Government, without popular information, or the means of acquiring it, is but a Prologue to a Farce or a Tragedy” and John F. Kennedy as explaining that a “nation that is afraid to let its people judge the truth and falsehood in an open market is a nation that is afraid of its people.”

The following is the full text of the Judge’s order, a copy of which is also available here.

UNITED STATES DISTRICT COURT

PHMPT, Plaintiff v. FDA, Defendant, No. 4:21-cv-1058-P

ORDER

This case involves the Freedom of Information Act (“FOIA”). Specifically, at issue is Plaintiff’s FOIA request seeking “[a]ll data and information for the Pfizer Vaccine enumerated in 21 C.F.R. § 601.51(e) with the exception of publicly available reports on the Vaccine Adverse Events Reporting System” from the Food and Drug Administration (“FDA”). See ECF No. 1. As has become standard, the Parties failed to agree to a mutually acceptable production schedule; instead, they submitted dueling production schedules for this Court’s consideration. Accordingly, the Court held a conference with the Parties to determine an appropriate production schedule.[1] See ECF Nos. 21, 34.

“Open government is fundamentally an American issue” – it is neither a Republican nor a Democrat issue.[2] As James Madison wrote, “[a] popular Government, without popular information, or the means of acquiring it, is but a Prologue to a Farce or a Tragedy; or, perhaps, both. Knowledge will forever govern ignorance: And a people who mean to be their own Governors, must arm themselves with the power which knowledge gives.”[3] John F. Kennedy likewise recognized that “a nation that is afraid to let its people judge the truth and falsehood in an open market is a nation that is afraid of its people.”[4] And, particularly appropriate in this case, John McCain (correctly) noted that “[e]xcessive administrative secrecy . . . feeds conspiracy theories and reduces the public’s confidence in the government.”[5]

Echoing these sentiments, “[t]he basic purpose of FOIA is to ensure an informed citizenry, [which is] vital to the functioning of a democratic society.” NLRB v. Robbins Tire & Rubber Co., 437 U.S. 214, 242 (1977). “FOIA was [therefore] enacted to ‘pierce the veil of administrative secrecy and to open agency action to the light of public scrutiny.’” Batton v. Evers, 598 F.3d 169, 175 (5th Cir. 2010) (quoting Dep’t of the Air Force v. Rose, 425 U.S. 352, 361 (1976)). And “Congress has long recognized that ‘information is often useful only if it is timely’ and that, therefore ‘excessive delay by the agency in its response is often tantamount to denial.’” Open Soc’y Just. Initiative v. CIA, 399 F. Supp. 3d 161, 165 (S.D.N.Y. 2019) (quoting H.R. REP. NO. 93-876, at 6271 (1974)). When needed, a court “may use its equitable powers to require an agency to process documents according to a court-imposed timeline.” Clemente v. FBI, 71 F. Supp. 3d 262, 269 (D.D.C. 2014).

Here, the Court recognizes the “unduly burdensome” challenges that this FOIA request may present to the FDA. See generally ECF Nos. 23, 30, 34. But, as expressed at the scheduling conference, there may not be a “more important issue at the Food and Drug Administration . . . than the pandemic, the Pfizer vaccine, getting every American vaccinated, [and] making sure that the American public is assured that this was not [] rush[ed] on behalf of the United States . . . .” ECF No. 34 at 46. Accordingly, the Court concludes that this FOIA request is of paramount public importance.

“[S]tale information is of little value.” Payne Enters., Inc. v. United States, 837 F.2d 486, 494 (D.C. Cir. 1988). The Court, agreeing with this truism, therefore concludes that the expeditious completion of Plaintiff’s request is not only practicable, but necessary. See Bloomberg, L.P. v. FDA, 500 F. Supp. 2d 371, 378 (S.D.N.Y. Aug. 15, 2007) (“[I]t is the compelling need for such public understanding that drives the urgency of the request.”). To that end, the Court further concludes that the production rate, as detailed below, appropriately balances the need for unprecedented urgency in processing this request with the FDA’s concerns regarding the burdens of production. See Halpern v. FBI, 181 F.3d 279, 284–85 (2nd Cir. 1991) (“[FOIA] emphasizes a preference for the fullest possible agency disclosure of such information consistent with a responsible balancing of competing concerns . . . .”).

Accordingly, having considered the Parties’ arguments, filings in support, and the applicable law, the Court ORDERS that:

1. The FDA shall produce the “more than 12,000 pages” articulated in its own proposal, see ECF No. 29 at 24, on or before January 31, 2022.

2. The FDA shall produce the remaining documents at a rate of 55,000 pages every 30 days, with the first production being due on or before March 1, 2022, until production is complete.

3. To the extent the FDA asserts any privilege, exemption, or exclusion as to any responsive record or portion thereof, FDA shall, concurrent with each production required by this Order, produce a redacted version of the record, redacting only those portions as to which privilege, exemption, or exclusion is asserted.

4. The Parties shall submit a Joint Status Report detailing the progress of the rolling production by April 1, 2022, and every 90 days thereafter.[6]

SO ORDERED on this 6th day of January, 2022.


[1] Surprisingly, the FDA did not send an agency representative to the scheduling conference.

[2] 151 CONG. REC. S1521 (daily ed. Feb. 16, 2005) (statement of Sen. John Cornyn).

[3] Letter from James Madison to W.T. Barry (August 4, 1822), in 9 WRITINGS OF JAMES MADISON 103 (S. Hunt ed., 1910).

[4] John F. Kennedy, Remarks on the 20th Anniversary of the Voice of America (Feb. 26, 1962).

[5] America After 9/11: Freedom Preserved or Freedom Lost?: Hearing Before the S. Comm. on the Judiciary, 108th Cong. 302 (2003).

[6] Although the Court does not decide whether the FDA correctly denied Plaintiff’s request for expedited processing, the issue is not moot. Should the Parties seek to file motions for summary judgment, the Court will take up the issue then.

from:    https://www.zerohedge.com/covid-19/judge-rejects-fdas-75-year-delay-vax-data-cuts-8-months?utm_source=&utm_medium=email&utm_campaign=399