COVID-19 HUMANITY BETRAYAL MEMORY PROJECT: Document Your Story

Crimes Against Humanity

We are witnessing crimes against humanity taking place all across this country and all over the world. Our friends and family members have been and are being harmed by measures ostensibly implemented to protect them and keep them safe.
We are witnessing crimes against humanity taking place all across this country and all over the world. Our friends and family members have been and are being harmed by measures ostensibly implemented to protect them and keep them safe.

Document Your Story

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Click link to document your story in the COVID-19 HUMANITY BETRAYAL MEMORY PROJECT.

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Source: https://chbmp.org/document/

DOCUMENTED CASES

Crimes Against Humanity
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Click link below to view documented cases in the COVID-19 HUMANITY BETRAYAL MEMORY PROJECT.

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Crimes Against Humanity

We are witnessing crimes against humanity taking place all across this country and all over the world. Our friends and family members have been and are being harmed by measures ostensibly implemented to protect them and keep them safe.

Two Years of Isolation, Abuse & Mistreatment

For over two years, the people have been abused, manipulated, maligned, and sometimes even murdered in the name of public health. This has been and is still going on in hospitals, assisted living facilities, juvenile detention centers, schools, and really anywhere else that institutional mandates can be applied with force. We, the people harmed by these unamerican and unconstitutional measures, are dedicated to pushing back on this encroachment on our civil liberties, and putting a stop to these grievous harms the people are being forced to endure at the hands of those entrusted to protect them.

Never Forget

This is one of many projects developed to defend our liberties undertaken by the FFFF. The primary goal of this project is to document, archive, and assist those impacted by these crimes against humanity. We are taking testimonials from those who have survived the protocols mandated by these disastrous policies, interviewing victims and family members to validate their stories, and documenting and archiving everything. We will not allow the victims of these crimes against humanity to go unheard.

Managed By FFFF Citizens Task Force 

The FFFF Task Force is composed of survivors, victims, and families of victims who have suffered grievous harm as a result of malicious public health policy. If you have been harmed by the disastrous public health policies of the last two years and would like to help others and raise awareness, please Join the FFFF Task Force today.

Source: https://chbmp.org/document/

mRNA Vaccines and EUA

open.substack.com/pub/rwmalonemd/p/mrna-vaccines-and-eua

mRNA Vaccines and EUA by Dr. Robert Malone

Whatever you may currently think about the SARS-CoV-2 vaccines, it is a fact that more than 5.41 billion people worldwide have received a dose of some type of COVID-19 vaccine, equal to about 70.5 percent of the world population.  In the United States as of October 17, 2022, 494.74 million “initial protocol doses” of SARS-CoV-2 vaccine have been administered, together with 138.16 million “booster” doses. 265.59 million US residents have received at least one dose, and 226.59 million have completed the initial vaccination protocol (see this link), out of a total population of 335.49 million (67.5%). In terms of the logistics of development, manufacturing and deployment of a novel injectable biologic product, this is undeniably a major achievement.

Of the SARS-CoV-2 mRNA vaccine doses administered in the United States as of October 19, 2022:

375.64M doses of Pfizer/Bio-N-Tech 237.61 doses of Moderna

Total U.S. of 613.25M mRNA vaccine doses administered. 

In the European Union, the corresponding numbers are:

641.89M doses of Pfizer/Bio-N-Tech 153.16M doses of Moderna

EU total of 795.05M mRNA vaccine doses administered

Grand Total of 1 Billion

408.3 million doses of mRNA vaccines in these two regions. All this involves a novel technology, product and large scale manufacturing process which was created, passed non-clinical and clinical development and was massively manufactured, distributed and globally deployed in less than three years.

At a meeting of the Special Committee of the European Union Parliament held on 11 October 2022 to discuss the findings regarding COVID-19 pandemic and recommendations for the future, a Pfizer executive confirmed that the vaccine had never been tested for its ability to prevent the transmission of SARS-CoV-2 virus before being put on the market. Data emerging since the introduction of the vaccine indicates that it is in fact unable to do so, thereby refuting the claim that the COVID-19 Passports provide any guarantee of protection.  In other words, although governments throughout the world employed a wide range of propaganda and censorship methods to promote these products as both safe and effective at stopping the spread of SARS-CoV-2 infection, there were no studies performed prior to this distribution which even tested how well the products would prevent the spread of COVID-19 disease.  It is not an exaggeration to state that this massive deployment has been the largest clinical experiment performed on human beings in the history of the world. 

All of the mRNA vaccine doses administered in the United States (to both citizens and military personnel) have been provided under “Emergency Use Authorization” (EUA), which is to say that although the FDA has licensed the Pfizer/Bio-N-Tech and Moderna vaccines for some age cohorts, the firms have elected to not manufacture, distribute, or market these licensed products in the United States.  The reason for this is not clear, but appears to relate to both liability issues as well as conditions placed by the FDA involving additional clinical studies, safety monitoring (pharmacovigilance)  and product disclosures once the products begin to be marketed.

From the standpoint of the vaccine manufacturers, EUA is a preferred pathway for marketing their products.  A single purchaser (the US Government) provides complete liability indemnification, a guaranteed market with very little oversight, and manages both the distribution and marketing.  In the case of all unlicensed products, the manufacturers are prohibited from marketing them, but under EUA the US Government has been doing this for them, and has been acting in coordination with corporate media, social media, and large technology firms to suppress any discussion of risks or limitations of the products.  From the standpoint of the vaccine manufacturers, this is all profit and no risk; a perfect business model.  Why would they ever want to consider taking up the burden of actually producing and marketing the licensed version of these products?

EUA is a process defined by US federal law (21 U.S. Code § 360bbb–3 – Authorization for medical products for use in emergencies) which in the case of these mRNA-based products involves biological products which are not approved, licensed, or cleared for commercial distribution.  Specifically, the statute authorizes “the introduction into interstate commerce, during the effective period of a declaration under subsection (b), of a drug, device, or biological product intended for use in an actual or potential emergency.”  Continued “Emergency Use Authorization” of these vaccines requires “a determination by the Secretary of Homeland Security that there is a domestic emergency, or a significant potential for a domestic emergency, involving a heightened risk of attack with a biological, chemical, radiological, or nuclear agent or agents”. Once the domestic emergency has passed (ergo “a determination by the Secretary, in consultation as appropriate with the Secretary of Homeland Security or the Secretary of Defense, that the circumstances described in paragraph (1) have ceased to exist”),  “A declaration under this subsection shall terminate”.  In other words, when there is no longer an emergency, the “Emergency Use Authorization” for the product will cease, and the vaccine products will return to their status as not approved, licensed, or cleared for commercial distribution.  These products remain experimental, and are only to be used for a limited amount of time during an ongoing emergency. 

“Pseudouridine likely affects multiple facets of mRNA function, including reduced immune stimulation by several mechanisms, prolonged half-life of pseudouridine-containing RNA, as well as potentially deleterious effects of Ψ on translation fidelity and efficiency.”

Based on the currently available information, it appears to me that the extensive random incorporation of pseudouridine into the synthetic mRNA-like molecules used for the Pfizer/BioNTech and Moderna SARS-CoV-2 vaccines may well account for much or all of the observed immunosuppression, DNA virus reactivation, and remarkable persistence of the synthetic “mRNA” molecules observed in lymph node biopsy tissues (Roltgen et al. 2022). Many of these adverse effects were reported by Kariko, Weissman et al in their 2008 paper  “Incorporation of pseudouridine into mRNA yields superior nonimmunogenic vector with increased translational capacity and biological stability” (Kariko et al. 2008) and could have been anticipated by regulatory and toxicology professionals if they had bothered to consider these findings prior to allowing emergency use authorization and widespread (global) deployment of what is truly an immature and previously untested technology.  Therefore, neither the FDA, NIH, CDC, nor BioNTech (which employs Dr. Kariko as a Vice President) nor Moderna can claim true ignorance.  To my eyes, what we have seen is more appropriately classified as “willful ignorance”.

Based on my review of the scientific data, it is my opinion that the random and uncontrolled insertion of pseudouridine into the manufactured “mRNA”-like molecules creates a population of polymers which may resemble natural mRNA, but which have a variety of properties which are clinically relevant. These characteristics and activities may account for many of the unusual effects, unusual stability, and striking adverse events associated with this new class of vaccines. These molecules are not natural mRNA, and they do not behave like natural mRNA. 

The question that most troubles and perplexes me at this point is why the biological consequences of these modifications and associated clinical adverse effects were not thoroughly investigated before widespread administration of random pseudouridine-incorporating “mRNA”-like molecules to a global population. 

Biology, and particularly molecular biology, is highly complex and interrelated.  Change one thing over here, and it is really hard to predict what might happen over there. That is why one must do rigorously controlled non-clinical and clinical research. Once again, it appears to me that the hubris of “elite” high status scientists, physicians and governmental “public health” bureaucrats has overcome common sense, well established regulatory norms have been disregarded, and patients have unnecessarily suffered as a consequence.  These products do not use natural mRNA, and referring to them as mRNA vaccines is misleading.  I recommend that, in the future, these products which employ a synthetic unnatural polymer which is not natural mRNA, should be designated using a different term, such as Ψ-mRNA genetic medicines.

The Forgotten Side of Medicine ~ How Corruption Dictates the Practice of Medicine

Steve Kirsch recently wrote an excellent article highlighting three “scientists” whose guideline recommendations were ultimately responsible for the deaths of nearly a million Americans. 

To summarize: It shows that there are dozens of treatments for COVID-19 that have numerous peer reviewed studies demonstrating their efficacy.  Despite those existing therapeutics and countless petitions for their usage, the committee responsible for developing the guidelines on what is an appropriate treatment for COVID-19 has only approved remdesivir, which is a toxic drug with no therapeutic value for treating COVID-19.  As a result, a dangerous drug has been mandated, while many drugs that would save lives are prohibited in most medical systems.

Evidence based medicine is commonly thought to mean “the best evidence” dictates the standard of care. In reality, it typically means financial interests dictate the standard of care and “evidence” is just used as a smokescreen to justify profiteering. This table that I initially discovered from Kirsch’s article provides clear and unambiguous proof of that contention. See if you can figure out what the circled drugs (those which received an EUA) all have in common!

Because I expected the conflicts of interests of the committee that determined the COVID-19 treatment guidelines to follow the typical pattern, I did some digging and discovered a lovely web of corruption that entangled many of its members.  The purpose of this article is to explain the typical pattern and illustrate how it was followed in this case.  I am doing this because I believe the first step to moving beyond that pattern is to recognize its existence. For those of you who do not need the context, please skip ahead to the COVID-19 Treatment Guidelines section.

Introduction

There are two ways you can observe most organizational systems:

•As someone trapped inside the system observing their surroundings.

•As an outside observer who sees the entire system as a whole.

Since we typically do not explore or examine systems that are outside our everyday lives, we will typically experience the first type of observation. This occurs after life circumstances force us to become stuck in a system, which happened to many of us who were swept into the maelstrom of COVID-19.

Two of my central principles for understanding the architecture of modern society have been the relentless creation of hierarchal systems and the monopolization of resources that are essential for life. 

In regard to the first principle, no matter where you look, a typical pattern is always followed: a hierarchy is established, significant investment is created to establish the importance of the hierarchy, and the top of the hierarchal pyramid is bought out (often through bribes) so that a small investment at the top can be leveraged to control an entire population. 

In regard to the second, those with obscene fortunes seem to always find ways to monopolize resources essential for life and transform them from something each person can independently produce to something they must continually work to obtain. For example, it is extremely common after communist revolutions that the independent farmers in the nation will either be prohibited from farming or executed, allowing agriculture to be transitioned to a state-run enterprise.  Once this happens, everyone is forced to work for the state or starve, which leads them to becoming obedient subjects that can be easily exploited for their labor.

In most cases when the monopolization of a life essential resource occurs, the new approach is hailed as a technological miracle and this is used to encourage people to let go of their traditional and self-sufficient approach. The new “miraculous” approach is initially deemed “superior” but before long turns out to be worse than the now abandoned initial approach.

The Green revolution is an excellent example of this (more and more fertilizers herbicides and pesticides are needed to produce the same agricultural input). For example, Bill Gates, under the guise of “charity,” has frequently made people in Africa abandon their traditional self-sufficient forms of agriculture and switch to modern chemical-intensive industrial agriculture. Before long, this spikes their price of food and farming supplies (which must be purchased from a multinational corporation like Monsanto). As we are now hitting an unprecedented global wave of fertilizer and food inflation, it is likely that millions who were coaxed into abandoning their traditional forms of agriculture will starve to death.

I have similar reservations about our current transition to green energy technologies. I know of numerous proven effective technologies that could lessen the environmental impact of our energy consumption. However, none of the technologies currently being evaluated meet this fundamental criteria. Instead, each one further centralizes control over this life essential resource, and in the future will likely be used to significantly limit unauthorized consumption of energy or transportation once our existing fossil fuel infrastructure is displaced. For example in light of recent political developments, concerns have begun to be raised over the switches existing in electric cars that can turn them off remotely.

Medical Inflation

Those two principles (rigid hierarchal organization and monopolization of a life essential resource) also happened with the medical industry and really kicked into gear when the Rockefellers (and to some extent Carnegie) bought the AMA and invested a great deal of money into standard medicine (often called “allopathic” or “biomedical” medicine).  A variety of competing schools of medicine were removed from the United States, and the practice of medicine was monopolized (those curious to learn more can find more details in this freely available classic).

This proved to be an excellent investment and the effect of this monopolization is striking:

Numerous changes in society emerged to support this medical paradigm. Some of the most important were as follows:

•Society was conditioned to believe that they needed a doctor to be healthy, rather than health being viewed as something each individuals was empowered to seek for themselves. This effectively created an unlimited demand for medical services, and as the above graphs show, an ever-growing need for medical spending. Medical Nemesis by Ivan Illich was the earliest work I was able to locate detailing this change and its consequences.

•Things that genuinely improve public health (and thereby reduce medical expenses) are typically not allowed to emerge, while pointless initiatives that do not improve public health (water fluoridation or annual flu shots) are continually promoted. Likewise, basic health education is not taught to most people, and instead health behaviors developed by corporate interests constitute the majority of “health education” (industry funded nutrition textbooks for example are very common in college courses). In short, there are dozens of simple and obvious policy changes that many have independently identified which could rapidly improve public health and save a lot of money, but despite decades of campaigning to enact them, most have never been adopted.

•Hundreds (or possibly thousands) of highly effective medical treatments for common diseases have been kept off the market to preserve the market for expensive but ineffective treatments that often require lifelong purchasing. For example, prior to the legislative battle to legalize acupuncture, I remember cases where Chinese immigrants were raided at gunpoint for practicing acupuncture in their own community without a license. For those interested, I’ve spent decades tracking those “forgotten cures” down, and while I have found many that for one reason or another were oversold and didn’t really work, I also found many others that were highly effective.

•Every medical service or product is designed to encouraged the consumption of more medical services or products.

•A rigid hierarchy was created to support this monopoly.

Medical Hierarchies

The first hierarchy relates to the right to practice medicine. A large debate exists over whether or not a license should be required to practice medicine. The trade-off is that if no license is required, unqualified practitioners who might harm the public are allowed to practice, while if a license is required, the practice of medicine is monopolized (making medicine much more expensive) and medical practitioners are unable to provide life saving medicines they believe in.

I will now examine a few levels of this hierarchy:

•Medical boards have the power to pull the licenses (and hence careers) of any physician who does something “bad.” Unfortunately, since medical board members are directly appointed by governors, they often end up with crooked and corrupt members (one colleague who served on a midwestern medical board attested to this). Some of the reasons why medical boards exercise their authority are definitely valid, but many others are done to target physicians who step outside the line of what prevailing interests want done. This has happened for a long time. Here are a few examples:

1. After SB 276 was signed in 2019, writing vaccine exemptions was for all practical purposes outlawed in California and I heard of numerous cases where doctors wrote a single justified exemption and then had their license terminated. For this reason, doctors in California will not even write exemptions for patients who nearly died from their first COVID-19 vaccine (ie. from anaphylaxis or a heart attack).

2. The federation of state medical boards put out a statement that publicly promoting any type of COVID “misinformation” (ie. mask efficacy, early treatment options, vaccine safety concerns) could be used to take away a physician’s license.

3. Physicians have had their license suspended for using early treatment options that have FDA approval for other conditions.

The experiences of Robert Malone’s colleague Meryl J. Nass MD is a well known example of the above, but there are many others as well.

As you might imagine, it is quite easy for corporate interests to influence the composition of medical boards (as they are composed of individuals appointed by the governor). In the late 1990s the opioid manufacturers concocted the idea of having present levels of pain be the 5th vital sign and hence measured at every visit.

Since their opioids had “no addictive potential” once this epidemic of “unrecognized” pain emerged (since everyone was encouraged to say they were in pain) the manufacturers managed to lobby the medical boards into taking the position that failing to treat pain with an opioid as malpractice. Once that happened, to protect their licenses, any physicians who had hesitations providing opioids to patients started giving out opioids like candy and this created the current opioid epidemic which has been beyond devastating for many poorer regions of the USA. The problem is massive; hundreds of thousands of people have died from drug overdoses since COVID (which is a figure comparable to the death count from COVID).

•It is very difficult for physicians to work privately in independent practice (a variety of factors have been put in place to force this change over the last 10-20 years). Instead they are required to work at corporate, federal or state jobs where they are largely at the mercy of the institution they work for to follow its policies.

It is for this reason that as soon I was able to, I stopped working for an institution that controlled my practice of medicine.

During the pandemic, many physicians who had serious concerns about the existing approach towards COVID-19 attempted to do things differently, and were frequently shut down by their institution. This led to physicians being fired for not telling their patients the vaccine was “safe and effective” and others such as Paul Marik MD having to sue their hospital in order to be permitted to prescribe a treatment they felt could save the lives of their patients (where no effective treatment was currently available and the patients were frequently expected to die otherwise). Trump’s “Right to Try” law was meant to address this issue, but corporate management has largely superseded it.

•Everyone in medicine is taught to defer to the judgement of a doctor. Hence if you want to do some type of medical treatment and the doctor does not “approve” it, you can’t. In nursing textbooks, it is repeatedly hammered in to always defer to a doctor’s judgement. Nurses typically spend significantly more time with patients where they can see and in their hearts question the human cost of an enforced medical regimen. In contrast, physicians (the ones with authority over the patient), due to their time constraints, typically spend very little time with their patients and are much more detached and isolated from them. This results in bypassing the human connection that should be necessary in medical decision making being bypassed. This type of organizational structure has been used in numerous inhumane systems in the past.

Similarly, many individuals who have found their loved ones in the hospital have been told that unless the supervising doctor approves it, they cannot have any other type of therapy administered. Since many hospitals would not change their policy, numerous lawsuits have been filed to permit patients expected to die to receive ivermectin for example. To my knowledge, in each case where the lawsuit ordered ivermectin to be administered, the drug then saved the patient’s life.

To further illustrate this hierarchy, I know a few physicians with active medical licenses who were hospitalized for COVID-19. Each told me during their hospital stay their that care was continually mismanaged, they had to constantly be on the alert for a fatal medical error, and many of their reasonable requests were not approved by the doctor supervising their hospital care.

•Medical schools to a large extent select for individuals who do not challenge the system, and once in medical school, they rigidly target anyone who is not compliant and obedient to the existing hierarchy to ensure that they will not graduate.

The medical education process is extremely difficult (you have to work brutal hours which break a certain number of medical students and resident physicians each year, and suicide is quite common) and many aspects of the education could be equated to a form of hazing. These types of experiences are known to produce subservience to a system and have been utilized in many fields besides medicine throughout history.

Finally, there is a massive financial cost to become a doctor (most physicians now graduate with between $200,000 to $400,000 of debt at ~7% interest) which leaves many doctors who want to do things differently being completely unable to challenge this system.

The second hierarchy is “medical evidence.” When evidence based medicine was initially introduced, it was a very good and needed paradigm. Many horrific and harmful practices were in wide usage that evidence based medicine had relegated to the dustbins of history. However, medical evidence also follows a hierarchy which rejects foreign or competing ideas, and the upper levels of this hierarchy is bought out by pharmaceutical interests. Here are some examples:

•In order for a study to “matter,” it has to be published in a prestigious journal. The problem is that with the occasional exception of the British Medical Journal, none of the prestigious journals will ever publish studies which go against the existing narrative. “Controversial” studies that merit publication are continually rejected, while bad studies that support mainstream views are regularly published.

One of the better-known recent examples involved The Lancet publishing a study showing hydroxychloroquine was unsafe and ineffective, which was used to end trials of HCQ globally. This study used blatantly fake data and was eventually retracted after readers complained.

The Journal of the American Medical Association appears to be the most biased publication in this regard, and in most cases you can predict what an entire article will say on a topic before you even read it (ie. does the COVID vaccine have any possible harm associated with it…no). The one interesting exception I have seen to this was a recently published study debunking the use of ivermectin. Here the conclusion of the article argued against the use of ivermectin, while the actual data argued for it, raising the possibility the authors phrased the conclusion to say the opposite of their results so that JAMA would publish the study (it is very common for conclusions in journal articles to not be representative of their results).

•In order for a study to be published in most journals, it has to pass “peer review.” In most cases, peer review will hold ideas challenging the existing narrative to either a high standard or an impossible-to-meet standard. Conversely, if an idea agrees with existing narratives, it is held to a very low standard in order to be published. This is an extremely common issue and why much of the most useful research I come across is not published in peer reviewed journals.

•In order for a study to be conducted, it frequently needs approval from the FDA (or an equivalent) and in most settings needs approval from an Institutional Review Board (IRB). In general, it is very difficult to get approval from the FDA to conduct any type of study unless a lot of money is behind the endeavor (for example I was familiar with multiple teams who had safe and effective treatments for COVID with supporting data that nonetheless could not receive FDA approval to begin their human trials). Similarly, despite the fact that extremely unethical human experiments are often conducted under an IRB, IRBs typically will not approve “controversial” research, leading to it not being done.

As a result, I frequently hear of fascinating therapeutic discoveries made outside the normal research process through trial and error that greatly benefit those who receive them, but in most cases these approaches can never be published because no IRB is willing to evaluate them. An excellent 2016 article published by the Association of American Physicians and Surgeons (a group that has also continually advocated for COVID patients) summarizes how many actually useful medical discoveries are made in independent clinical practice, but the recent hierarchal shifts in medicine have made it so this process is becoming continually rarer and rarer.

The accepted practice of medicine is also a hierarchy largely dictated by “medical evidence.” The existing hierarchal structure here makes it so that contrary research that does end up being published nonetheless is prevented from challenging the status quo. I will review some key examples:

•Medical practice is largely determined by “guidelines” that each physician is expected to follow. In most cases if you follow existing guidelines (ie. don’t treat someone with COVID until they have respiratory failure, then put them on a ventilator and give them remdesivir), you get paid and cannot get in trouble. If you do not follow guidelines, it becomes possible for you to be sued for medical malpractice, health care systems will fire you, and medical boards may take your license.

To illustrate physician attachment to guidelines: Throughout the pandemic I have participated in an online forum that approximately 100,000 US healthcare workers use. As you would imagine, the general mentality there is very conventional. One of the more interesting things I noticed in the early days of the pandemic was health care providers desperately asking for and enthusiastically sharing COVID-19 treatment guidelines from various academic institutions, while at the same time aggressively shooting down independent suggestions or ideas raised by individual physicians.

Guidelines are supposed to be made by impartial committees of experts tasked with reviewing the existing evidence in order to determine the most appropriate guidelines. In reality, as pointed out in Steve Kirsch’s article, these committees are extremely biased, and selectively choose evidence supporting the prevailing narrative.

In most cases, the decision of these unelected guideline committees goes unchallenged and even though they should not be (as discussed later), they are in effect the law.

The only exception I know of occurred when the Lyme community sued the Infectious Disease Society of America (which has also published widely cited COVID treatment guidelines I and others strongly disagree with). The lawsuit challenged IDSA’s guidelines that argued against the use of antibiotics for chronic Lyme disease, which was frequently being used by insurers to deny payment for those treatments and as a basis for authorities to crack down on those treatments being administered in private practice.

•Many people can only afford medical care covered by their insurance. In most cases, insurance will only pay for treatments supported by guideline committees and forces providers to spend most of their time fulfilling requirements of the insurance companies rather than treating patients. As you would imagine, significant financial entanglements exist between hospital systems, pharmaceutical companies and insurance companies (for example they often share interlocking board members), which further incentivizes specific therapeutic approaches.

The insurance dynamic creates the unfortunate situation where many people who need help for a condition must depend on word of mouth to identify a physician outside the insurance system who they have to pay for out of pocket. Provided they find the right physician and can afford their care (each of which is often not the case), these individuals often are able to recover from their illness.

•Reciprocally, insurance companies will often pressure health care providers to perform certain services for each patient that “improve quality of care.” If you follow those suggestions (which frequently results in most of the visit being taken up to do so), you are paid more by the insurance companies. Since everyone in health care is tight on money, those incentives result in significant pressure being put on physicians from their administrators to follow those suggestions.

The problem is that many of these suggestions encourage doing things I do not believe help patients and often harm them. For example, one of the reasons doctors aggressively push vaccines to their patients is because insurance companies pay them significantly more for all visits if most of their patients (especially children) are vaccinated. Similarly, one of the reasons why hospitals have been so aggressive in forcing ventilation and remdesivir (to the point they will fight expensive lawsuits to continue doing so), is because Medicare, in accordance with the COVID treatment guidelines, pays them a lot more to manage (and then kill) their patients in this way.

•Federal, state and municipal law enforcement authorities will frequently target those who promote treatments that violate guidelines. In my own experience (and for many others), IV vitamin C has been extremely helpful in certain (but not all) COVID cases. There is also research showing a benefit in COVID from this therapy Nonetheless, the guidelines recommend against it and individuals who publicly promoted IV vitamin C (at a time when no treatment for COVID-19 was available) had their clinics raided and were criminally charged.

•The media will attack any controversial treatment by claiming there is no evidence for it, and simultaneously refuse to report any evidence that emerges in favor of it. Likewise, Big Tech aggressively censors anything that goes against the existing medical narrative. For example, early in the pandemic, a video was posted by a leading researcher who had conducted clinical trials on using IV vitamin C for COVID-19 presenting his data to the NIH. This video was removed by Youtube shortly afterwards for violating their COVID misinformation policy.

How the Hierarchy is Bought Out

As you might imagine, the hierarchy outlined before is immensely susceptible to bribery. As so much money is in health care, this is what always happens.

•When the Affordable Healthcare Act was passed in 2010, its goal was to make health care more affordable. In 2009, total USA healthcare costs were 2.6 trillion dollars. In 2020 it was 4.3 trillion dollars (compared to wages going from $40,711.61 to $55,628.60 per the SSA). As this data shows, Obamacare failed its stated objective. I believe the central problem with Obamacare was that the medical industry is the largest lobbyist in Congress. Because of this, they were able to craft Obamacare to benefit their industry and thereby remove each provision that would have achieved the stated goal of the Affordable Health Care Act, leaving us instead with a variety of highly problematic federal regulations.

•The pharmaceutical industry is the largest sponsor of the mainstream media. For this reason, they prevent stories critical of pharmaceutical products from being discussed and regularly air stories promoting pharmaceuticals. Likewise, they will relentlessly attack anything that opposes mainstream pharmaceutical positions (frequently “cancelling” it and labelling it unscientific and without evidence). During COVID-19 this trend has accelerated following the Biden administration dispensing 1 billion dollars to news outlets across the political spectrum in return for positive coverage of the vaccine. I do not know of any past precedent for this.

Many journalists have complained about their inability to criticize dangerous pharmaceutical products, and to my knowledge, Tucker Carlson is the only individual with a mainstream platform who has (occasionally) spoken out against the industry. In recent times Big Tech and Big Pharma (who during Obama’s presidency became the core sponsors of the Democrat Party) have financially merged with each other, and like the media Big Tech now has a similar commercial interest in protecting Big Pharma’s monopoly.

•Most medical journals are primarily funded by pharmaceutical companies. Because of this, there is a strong bias to publish questionable industry sponsored trials. Conversely, there is also a strong bias to not publish data supporting alternative therapies that challenge their sponsors (an early example of this this is explicitly detailed and can be found within the 2001 book Heart Frauds but I am sure many earlier ones exist). As many of you have noticed, this publication bias has gone into overdrive throughout COVID-19.

•”Large randomized double-blind studies” are typically considered to be the best form of evidence, and many individuals will reflexively dismiss a study unless it fulfills that criteria. The problem is that these types of studies are immensely expensive to conduct, and in most cases can only be done if a pharmaceutical company sponsors them.

As you might expect, numerous studies have shown that when pharmaceutical studies are compared to noncommercial studies, industry studies tend to greatly overestimate the benefits of a drug and understate its harms. This is due to them having a large number of (fraudulent) tricks to create the “scientific” outcome they want. One of the best known recent examples concerned an article in the BMJ discussing a whistleblower who provided proof widespread fraud occurred during Pfizer’s vaccine trials.

While a small benefit can be attributed to the placebo effect (hence suggesting the need for a “placebo controlled trial), in most cases, the bias that emerges from the inherent conflict of interest in a pharmaceutically sponsored trial greatly exceeds the placebo effect. This is extremely important to understand, but rarely understood.

Even in non-blinded studies where a large magnitude of benefit is found (which greatly exceeds any possible placebo effect) those results are typically ignored or dismissed in favor of corporate sponsored research. A sad reality with many scientific publications is that if you read the author conflict of interest disclosures (which intentionally omit key details) and see who sponsored the study of the study, you can typically predict most of what will be written within the publication.

•Most researchers and academic institutions are extremely short on money. Because of this, they are forced to accept pharmaceutical money for any type of research they want to do, and in most cases not ask questions that will upset their sponsors (and even when honest researchers exist, administrators directly concerned with institutional finances will keep them in line). To a lesser extent, they can also function through public grants, but as detailed in “The Real Anthony Fauci” the grant system has been compromised so only researchers who support the mainstream narratives (and have not opposed Anthony Fauci) can get grants. Many respected scientists I have learned a great deal from, believe the corruption of the grant system, which Fauci is largely responsible for, has prevented American science from developing innovative scientific discoveries that were frequently developed in the past.

•In many cases, guideline committees are composed of individuals who have a direct financial conflict of interest over the guidelines they are promoting. The Lyme disease lawsuit for instance was filed on this basis. Malcom Kendrick an English physician who has done an excellent job illustrating many of the scams conducted by the pharmaceutical industry provided one of the best examples for this concept in his book Doctoring Data.

Many physicians are of the opinion statins (which lower cholesterol) have minimal benefit in preventing heart disease and expose patients to frequent and significant adverse effects, but since statins were put on the market, guideline committees have continually lowered the acceptable blood levels of cholesterol, thereby significantly increasing the pool of people who could take statins (leading to the situation that on almost any medical board examination, the correct answer is almost always “give the patient a statin”).

Kendrick’s specific example was that on the guideline committee responsible for determining who needed to receive statins in the United States, every single person who was on the committee (except the chair who was legally barred from it) had a financial conflict of interest with statin manufacturers. As you might guess, one of the quality metrics that administrators have held meetings on and which I was forced to attend regarded not enough “eligible” patients at the clinic being prescribed statin therapy.

•One of Fauci’s major achievements was turning the NIH and NIAID into pharmaceutical production pipelines. This was largely accomplished by allowing federal officials who were involved with the discovery or development of a pharmaceutical that went to market receive royalties for the drug once it was approved that often vastly exceed their salary.

As a result, there is an inherent conflict of interest to push unsafe or ineffective pharmaceuticals through the regulatory process. This frequently happens, whereas non-commercial enterprises focused on public good can almost never receive approval for a medication. Many outside observers believed based on the existing data, remdesivir should not under any circumstances have received an FDA approval, yet it did, largely due to the FDA electing to waive all the required safeguards (such as needing to consult an outside advisory panel) put in place to prevent something like this from occurring.

One of the most interesting aspects of this scheme (detailed in the Real Anthony Fauci) was that Fauci developed a large network of principal investigators (PI’s are needed to run clinical trials) who hold significant sway in getting IRBs around the country to approve ethically questionable trials needed to get unsafe drugs to market. The Real Anthony Fauci also discusses the retaliation faced by honest regulators who raise objections to problems with those trials.

In short, pharmaceutical companies have always bribed regulators, but Fauci had the unique accomplishment of transforming this into being an integral part of the HSS where the regulators would often take it upon themselves to solicit those bribes.

•Lastly, physicians in everyday practice are remarkably susceptible to being bribed, and a cornerstone of the pharmaceutical industry is sending sales reps to convince physicians to prescribe their medications. A small number of physicians refuse to see reps under any circumstances as they feel it is immoral for their own financial self interest to influence their treatment of patients. Typically however, pharmaceutical reps are remarkably effective at accomplishing their goal of selling their chosen medication and many academic physicians who widely promote pharmaceutical products receive immense payouts for doing so.

Revisiting HIV

In my initial post on this substack, I stated I was able to predict much of what has happened with COVID three months before the pandemic started. This was because I have found whenever a formula is discovered which “works” it is typically reused over and over.

The story of HIV, for those interested was originally detailed in Peter Duesberg’s book Inventing the AIDS Virus, and then subsequently further discussed in The Real Anthony Fauci. Fauci’s conduct during this period appeared to have laid the blueprint for what was done with COVID.

At the start of the HIV, there was no cure and many members of the gay community suffered severe disease or died. As time moved forward, independent physicians working in the community discovered a variety of effective treatments for the AIDS patients, some of which were alternative therapies, but most of which utilized repurposed FDA approved drugs. Like the stories shared in those books, a few of my own friends worked in HIV hot spots during this time, and each found they were able to save the lives of their patients if they abandoned government recommendations and tried their own protocols.

Despite endless requests to study these approaches, Anthony Fauci blocked every single one from being studied or adopted into standard of care. In parallel, he pushed along research on a highly toxic drug, AZT. AZT had originally been intended to be used for chemotherapy, but was abandoned as it proved to be too toxic.

While AZT should have never been approved, Fauci was eventually able to manipulate one (terrible) study enough that alongside sufficient pressure being applied to the FDA, earn AZT an FDA approval. Once AZT entered the market, as was obvious from the existing clinical trial data, it significantly worsened the prognosis for AIDS patients, something both reported in each of those books and also reported to me by a few colleagues who observed it enter the market. Despite being responsible for killing many members of the gay community (who at the time protested against Fauci for being a mass murderer), Fauci was hailed a hero, became one of the most influential members of the US government, and made a lot of money in the process.

COVID-19 Treatment Guidelines

At the start of COVID-19, the WHO made the curious announcement that Remdesivir would be the standard of care for COVID-19, despite almost no evidence existing to support this decision. After finding out the drug was a nonspecific viral RNA polymerase inhibitor, I became worried it would likely be somewhat toxic to cells, as broad spectrum antivirals tend to overlap with chemotherapy drugs (AZT being one example).

My initial suspicion was that Remdesivir would also affect cellular RNA polymerases (the classic example you learn in medical school are poisonous wild mushrooms triggering organ failure through this mechanism). As I began hearing of reports of organ failure near the start of the pandemic from physicians in China, I prayed we would not see a repeat of AZT. Since that time, significant evidence against Remdesivir has been uncovered suggesting it should have never been brought to market and to some extent, like AZT, it appears Remdesivir has caused significant harm.

As I observed the trajectory COVID-19 was headed in, I formed the hypothesis that a new lucrative drug needed to be put onto the market which could be theoretically argued to treat COVID-19 (“remdesivir must work since it is a non-specific viral RNA polymerase inhibitor”) but in reality would not be effective and instead would worsen and prolong the pandemic. I suspected this strategy would be adopted since the profit from selling the drug could be channeled into keeping effective therapies off the market long enough for vaccines to enter the market. This sadly appears to be what exactly happened once the COVID-19 Treatment Guidelines Panel of the NIH made remdesivir the standard of care for COVID-19.

Reference Link : A Midwestern Doctor / Substack

COVID Help: $300,000 to Study How Traditional College Grading Perpetuates Systemic Inequalities | Judicial Watch

COVID Help: $300,000 to Study How Traditional College Grading Perpetuates Systemic Inequalities

A public university is getting hundreds of thousands of dollars from the Biden administration’s fraud infested COVID relief fund to study how traditional grading in college perpetuates systemic inequalities toward nontraditional and rural students. “Common classroom practices, such as grading and the use of grades to assess knowledge and performance, may have unintended consequences on students who invariably derive an awareness of their own academic abilities from the results of those grading structures,” according to the National Science Foundation (NSF), which is doling out the money. “In fact, these traditional practices may inadvertently create and promote inequities among different student groups, particularly in large enrollment courses, but these issues have largely been unexplored.”

Beginning early next year, the agency will give North Dakota State University (NDSU) $300,000 to explore the phenomenon. The project is officially titled “Reimagining Grading to Support Nontraditional and Rural Students in High Enrollment, Gateway STEM Courses” and it will be funded by the American Rescue Plan of 2021, the nearly $2 trillion measure passed by Democrats to provide immediate and direct relief to families and workers impacted by the COVID-19 crisis through no fault of their own. When the law passed last spring, the Biden administration promoted it as one of the most progressive pieces of legislation in history that would build a bridge to an equitable economic recovery. The administration justified the measure by asserting that the public health crisis and resulting economic crisis devastated the health and economic wellbeing of millions of Americans, particularly people of color, immigrants, and low-wage workers.

The reality is that a lot of the money—billions and counting—has gone to unrelated causes and the administration’s monstrous taxpayer funded COVID relief program is rife with fraud and corruption. The problem is so bad that the Department of Justice (DOJ) created a COVID-19 Fraud Enforcement Task Force to “enhance efforts to combat and prevent pandemic-related fraud.” The special unit has been quite busy prosecuting a multitude of scams, false statements, and money laundering related to pandemic relief. This month House Republicans issued a report documenting 500 days of massive waste, fraud, and abuse in the American Rescue Plan. It includes more than $783 million in stimulus checks for convicted prisoners including the Boston Marathon bomber, $40 million to expand libraries in Delaware, $2 million for a Florida golf course and $16 million for electric vehicle charging stations in Maine and $20 million to modernize the state’s fish hatcheries. The list goes on and on.

The scathing report may seem like the $300,000 for the latest questionable project is a drop in the bucket, but it highlights that cash flow has not been deterred by waste. The NDSU researcher (Tara Slominski) who will conduct the study beginning next year claims in a university article that that traditional grading practices perpetuate systemic inequities for college students. “Her work will directly address this challenge by providing STEM faculty with equitable and practical assessment and grading approaches to better support today’s college students,” the piece states, adding that the work will create more equitable learning environments. Slominski teaches biology at NDSU and has already developed a curriculum to promote success among at-risk students. She claims that “the findings from this work will help faculty across the country and across disciplines create more equitable learning environments that are better suited to support the needs of today’s college students.”

The NSF, which funds more than a quarter of research conducted at American colleges with its $8.5 billion annual budget, explains that Slominski’s postdoctoral research fellowship project seeks to examine the impact of grading practices on self-concept and STEM persistence with a special focus on rural and nontraditional students. “The project has promise to produce new insights about equitable classroom and grading practices for rural and nontraditional students that are compatible with the constraints of high enrollment gateway courses,” the agency writes in the grant announcement. It is not clear how this may provide immediate and direct relief to families and workers impacted by the COVID-19 crisis through no fault of their own as the American Rescue Plan intended.
— Read on www.judicialwatch.org/grading-perpetuates-inequalities/

Dr. Zelenko – WWIII – Civil War on the Horizon & More Viruses Coming

Maria Zeee Uncensored
— Read on www.redvoicemedia.com/video/2022/05/dr-zelenko-wwiii-civil-war-on-the-horizon-more-viruses-coming/

Dr. Zelenko joins Maria Zeee to discuss World War III, the fact that he sees civil war as a real possibility due to the masses waking up to the reality of the Great Reset, the psychopaths behind the NWO and more viruses coming (backed by Bill Gates).

Yuval Hariri Tells You What The Vaccines Really Do

Yuval Hariri Tells You What The Vaccines Really Do

The guru of our corrupt globalist elite really hates human beings too

Emerald Robinson

20 hr ago

Let’s review what we do know about the new COVID gene alteration therapies that really distinguishes them from actual vaccines, shall we?

They don’t prevent you from getting COVID.

They don’t prevent you from spreading COVID.

They don’t limit the severity of COVID if you get infected.

In fact, they don’t do anything that vaccines are supposed to do. This raises aprofound question: what are they really supposed to do?

There happens to be an Israeli professor of history who has profoundly influenced Klaus Schwab and the global cartel of trans-humanist oligarchs — and he’s more than happy to tell you what the vaccines actually do. He’s the leading thinker, the arch-guru, of the Silicon Valley dictator set. His name is Yuval Hariri.

April 20th 2022

At one globalist conference, he explained exactly what the COVID pandemic was being used by the globalist elites to do: “COVID is critical because this is what convinces people to accept, to legitimize, total biometric surveillance. If we want to stop this epidemic — we need to not just monitor people, we need to monitor what is happening underneath their skin.”

Yuval Hariri has said similar things at many other conferences and lectures as well: “Maybe in a couple of decades, when people look back, the thing they will remember from the COVID crisis, is: this is the moment when everything went digital. This was the moment when everything became monitored — that we agreed to be surveilled all the time. Not just in authoritarian regimes but even in democracies. This was the moment when surveillance went under the skin.”

Do you see? COVID is not the “accidental” release of a bioweapon derived from a Chinese bat coronavirus — it’s actually an opportunity for governments and global corporations to create a total surveillance system around the world that will ultimately control every human being. 

This sounds like science fiction. It is not. There are secret ingredients in the COVID vaccines like graphene oxide (that the corporate media tells you is a conspiracy theory of course!) that can transmit data outside the body — like your heart rate.

What do the COVID vaccines really do? They usher in the Age of Total Surveillance.

Professor Hariri explained this new and terrifying reality (that he wants to usher into the world) to the World Economic Forum in 2018 where our corrupt elites embraced the idea that they would be the immortal masters of the world while they enslaved the rest of us in their new “digital dictatorship.”

Professor Hariri is not alone in his depravity — just check out what DARPA is working on. Needless to say: DARPA (and the Pentagon more broadly) is not really in the healthcare business and couldn’t be less interested in “healing bodies” more effectively. This is simply the cover, the excuse, for the radical intrusion into every sphere of human life which can only be called: totalitarian techno-fascism.

Hariri is not really a humanist either— he doesn’t have any love for humanity. Nor is he really interested in the preservation of democracy. He is the psuedo-prophet of a one world government that would enslave humanity forever using a version of communist China’s social credit system to keep the masses under control. 

For instance, Professor Hariri predicts a future where the machines we have created have no more use for humans (because of Artifical Intelligence) and so “by 2050 a new class of people might emerge – the useless class. People who are not just unemployed, but unemployable.” Why would we allow such a future? The premise of the question is not something Hariri explains for obvious reasons. Why would he? He’s on the side of the machines.

Technology is going to turn the Davos crowd into gods, and the working class into peasants to be eliminated as so many “useless eaters.” After all, we humans “should get used to the idea that we are no longer mysterious souls.” We are “hackable animals” so Hariri wants you to get ready to be hacked.

The best way to describe Hariri’s worldview is that he is a nihilist — but nihilism doesn’t really capture how dark and dangerous his thinking happens to be: “As far as we can tell from a purely scientific viewpoint, human life has absolutely no meaning. Humans are the outcome of blind evolutionary processes that operate without goal or purpose. Our actions are not part of some divine cosmic plan, and if planet earth were to blow up tomorrow morning, the universe would probably keep going about its business as usual. As far as we can tell at this point, human subjectivity would not be missed. Hence any meaning that people inscribe to their lives is just a delusion.”

People like Hariri who believe that nothing is real and that everything is permitted are the most dangerous people of all — traditional morality to them is simply a construct that only the weak obey. Hariri’s atheism wants to touch the abyss, and summon the darkness. Even his pessimism is pessimistic. For him, life has no meaning. Free will is an illusion. God does not exist. Religions are transparently absurd attempts to create meaning. Truth is a fiction — only power is real. Humanity is not to be pitied so much as controlled by a superior race of the wealthy and the powerful that (no surprise) enjoy paying exorbitant fees to hear Professor Hariri discuss their future as gods on earth.

Biohackinfo 🇸🇪 @biohackinfo “The really big revolution will be when the #AI Revolution merges with the #Biotech Revolution, and goes under the skin.” -Noah Yuval Hariri

Yuval Hariri has only one soft spot, and that’s for animals in our food supply. He’s a vegan apparently: “Domesticated chickens and cattle may well be an evolutionary success story, but they are also among the most miserable creatures that ever lived. The domestication of animals was founded on a series of brutal practices that only became crueller with the passing of the centuries.”

“Let’s enslave humanity, and spare the chickens” is a strange message because chickens and cattle are animals that should be spared in Hariri’s view — but then humans are animals too (Hariri says this again and again) but we don’t deserve any sympathy in the final analysis.

One can’t help but notice the obvious self-hatred contained in these elementary philosophical contradictions that any 5 year old child would notice instantly. Hariri is not a great thinker. He’s not even a sub-par historian. He’s the limp-wristed avatar of a globalist cabal (Bill Gates, Xi Jinping, Klaus Schwab, Larry Fink) that seeks to destroy Western democracies in order to rule behind the scenes like so many Wizards of Oz.

These people are, in other words, the enemies of all humanity.

REPORT: 33-Year-Old Mother Paralyzed Following COVID Jab

REPORT: 33-Year-Old Mother Paralyzed Following COVID Jab

Another day, another tragedy. It’s become an all-too-familiar story by now.

Her doctor, her government and the mainstream media – all assured her it would be OK, and that the new experimental mRNA synthetic pharmaceutical cocktail was ‘safe and effective.’ In a mere moment, her entire life turned on a dime.

Just 12 hours after receiving her experimental COVID-19 gene therapy injection manufactured by Pfizer, 33-year-old mother Rachel Cecere’s body began rebelling against her, and she was later diagnosed with “acute distress to the nervous system.” Rachel found herself paralyzed from the neck down, but three weeks later she was able to regain strength in her upper body, except for her left hand.

The timing of the onset of her disease just after receiving the experimental ‘vaccine’ is suspect to say the least. Was her disability brought on by the jab? If so, who will be held accountable?

She is not alone either. To date the various vaccine adverse reactions databases in the US, UK, and EU alone contain, on the aggregate, millions of reported injuries, as well as tens of thousands of deaths following the experimental shot.

She asks in desperation, “When is this going to get better?” Watch: 

This video was published at Odysee on February 2, 2022

READ MORE VACCINE NEWS AT: 21st Century Wire Vaccine Files

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Bad Things Coming for Those Responsible? – Pfizer and Moderna CFOs Run for the Exits

Merissa Hansen: The CFOs of Pizer and Moderna have both resigned over the past 72 hours.

Luke Rudkowski: “There were literal media organizations telling the [British] government to stop releasing the data in the United Kingdom, which showed that the vaccine actually [does more harm than good] in certain age groups… There’s a lot of ruling elites that want to keep your mind away from their KILLING of you, and they distract you with a lot of utter nonsense.”

Full Video: https://wearechange.org/mike-tyson-is-warning-about-rich-people-hunting-poor-people/

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Taschi Talks – Episode 15: Trust the Experts? ATAGI and the 4th booster.

Taschi reads through the ATAGI statement on recommendations on a winter booster dose of COVID-19 vaccine, with a critical eye. ‘Trust the science’ and ‘peer review’ is what we have repeatedly heard – but do the ‘experts’ follow their own advice? Have a listen!

Links:
https://www.abc.net.au/news/health/2022-03-25/atagi-covid-vaccine-fourth-shot-booster-immunity-omicron-variant/100939326
https://www.health.gov.au/news/atagi-statement-on-recommendations-on-a-winter-booster-dose-of-covid-19-vaccine
https://www.health.gov.au/committees-and-groups/australian-technical-advisory-group-on-immunisation-atagi
https://apps.tga.gov.au/PROD/DAEN/daen-report.aspx
https://www.tga.gov.au/auspar/auspar-bnt162b2-mrna-comirnaty
https://www.tga.gov.au/auspar/auspar-elasomeran
https://pubmed.ncbi.nlm.nih.gov/31607599/