Category Archives: Covid

The Story of Pfizer Inc.

A Case Study in Pharmaceutical Empire and Corporate Corruption

Article here.

Excerpts:

The extensive history of the pharmaceutical industry is filled with stories and deeds of adventures, misadventures, profit-making, profit-taking, fraud, bribery, false claims, messianic promises, and criminal conduct. 

Few companies in the history of medicine have received as much attention as Pfizer Inc. has received these last three years of the Corona Crisis.

Through the course of relentless media coverage and amidst all the sound and fury, Pfizer has managed to avoid scrutiny of its previous criminal conduct and is universally portrayed in the mainstream media as a benevolent enterprise whose mission is to nobly service humanity.

In an effort to set the record straight we embark upon a comprehensive historical examination of this company which sprouted from humble beginnings into one of the most influential corporate behemoths walking the earth today.

[. . .]

Given Pfizer’s documented record of misdeeds, any reasonable person would ask:

“Is this a company that belongs behind the wheel of the most widespread mass vaccination campaign in history?”

“Is this a company we should trust with experimental medical technology?”

“Is this a company we want to be in control of the most radical mass medical experiment in human history?”

“How is it that a company that habitually engaged in such illegal practices was able to reinvent itself as the savior of humanity?”

Charlatans in Science

A real life "Uncle Andrew"

See here.

Excerpts:

As an example of [Peter] Hotez’s repeat offenses, Dore plays a compilation video of Hotez, starting with Hotez pointing out there are “unique potential safety problems” related to coronavirus vaccines in 2020. Then, something happened and Hotez never admitted the possibility of safety problems again.

Instead, he started pushing the single-dose Janssen shot, which later got pulled in several countries due to life-threatening blood clots. Then he started pushing the two-dose mRNA shots, saying they offer “long-lasting” protection. Then, when the boosters rolled out, he switched to saying “I’ve always said this is a three-dose vaccine.”

Then, he argued “a fourth immunization” would be necessary “to keep the country going.” And when hospitals continued to fill up with COVID patients, he told people to get the bivalent booster.

After that, he started saying yearly boosters would be necessary, only to later change his mind saying we may need a booster “every few months,” because the boosters “aren’t holding up as well as we’d like.”

He also pushed the COVID jab on young children, claiming COVID was “picking off young people like we’ve never seen [before].” With a track record like that, proving yourself wrong every few months, criminalizing critique would surely be nice.

Eric Metaxas and “Letter to American Churches”

Discussion with Jordan Peterson

I haven’t heard of this author or his new book with the above title before but he sounds immensely interesting. Not least because he, having grown up in America, has a Greek (father) and German (mother) background. His mother having lost her father in the Second World War.

Here’s the video description:

Dr. Jordan B. Peterson and Eric Metaxas discuss his most recent book, “A Letter to the American Church,” which argues a betrayal of faith by those who stay silent in the face of tyranny. They parallel the arbiters of speech across history against those populating today, and detail the responsibility to act against falsehood that is intrinsically present in the Abrahamic tradition, yet increasingly absent in the American church today.

Eric Metaxas is an American author, speaker, and radio host. He has written award winning biographies, such as “Bonhoeffer,” as well as children’s books like “Squanto and the Miracle of Thanksgiving,” Metaxas hosts Socrates in the City, a recurring popular event where he interviews writers and thinkers on theology, moralism, and philosophy. He also hosts the nationally syndicated Eric Metaxas Show, more broadly referred to as “The Show About Everything.”

In the podcast (1 h 33 min, on Youtube here, on Bitchute here), Metaxas explains that in his new book he says that the American churches are making the same mistakes the German churches made in Nazi Germany. They looked the other way and narrowed themselves down to “thin theology”. Some did speak up, but not until it was too late to achieve anything meaningful.

(I would add that this “letter” should be addressed to churches “in the American Empire”, which includes the UK and all of Europe.)

Another thing he says is that churches that defied the Covid measures and stayed open during lockdowns “increased four to fivefold”, while those that locked down “withered”.

I can certainly believe that.

He has an amazing personal conversion story that involves a dream, at the age of 25, about picking a golden fish out of the water. He knew in the dream that the fish is Christ.

He has previously written an impressive number and range of books, including biographies about Dietrich Bonhoeffer, Martin Luther and William Wilberforce. According to Wikipedia, the latter was “the companion book to the 2006 film [on Wilberforce: Amazing Grace].”

In 2021, he published a book titled “Is Atheism Dead?” and last year the aforementioned “Letter to American Churches.”

This is more than a free speech crisis

It’s a humanity crisis, says Matt Taibbi

Matt Taibbi, a journalist who has been investigating how the FBI and other US authorities influenced Twitter during the pandemic to uphold a certain “narrative”, spoke recently to a Free Speech gathering in London. Below is an excerpt of what he said. The full text is here.

[. . .]

But after looking at thousands of emails and Slack chats, I first started to get a headache, then became confused. I realized the old-school Enlightenment-era protections I grew up revering were designed to counter authoritarianism as people understood the concept hundreds of years ago, back in the days of tri-cornered hats and streets lined with horse manure.

What Michael and I were looking at was something new, an Internet-age approach to political control that uses brute digital force to alter reality itself. We certainly saw plenty of examples of censorship and de-platforming and government collaboration in those efforts. However, it’s clear that the idea behind the sweeping system of digital surveillance combined with thousands or even millions of subtle rewards and punishments built into the online experience, is to condition people to censor themselves.

[. . .]

But it goes deeper. Michael and I found correspondence in Twitter about something called the Virality Project, which was a cross-platform, information-sharing program led by Stanford University through which companies like Google, Twitter, and Facebook shared information about Covid-19.

They compared notes on how to censor or deamplify certain content. The ostensible mission made sense, at least on the surface: it was to combat “misinformation” about the pandemic, and to encourage people to get vaccinated. When we read the communications to and from Stanford, we found shocking passages.

One suggested to Twitter that it should consider as “standard misinformation on your platform… stories of true vaccine side effects… true posts which could fuel hesitancy” as well as “worrisome jokes” or posts about things like “natural immunity” or “vaccinated individuals contracting Covid-19 anyway.”

This is straight out of Orwell. Instead of having “ambiguities” and “shades of meaning” on Covid-19, they reduced everything to a binary: vax and anti-vax.

They eliminated ambiguities by looking into the minds of users. In the Virality Project if a person told a true story about someone developing myocarditis after getting vaccinated, even if that person was just telling a story – even if they weren’t saying, “The shot caused the myocarditis” – the Virality Project just saw a post that may “promote hesitancy.”

So, this content was true, but politically categorized as anti-vax, and therefore misinformation – untrue.

[. . .]

“This continual process of seeding doubt and uncertainty in authoritative voices,” wrote Graphika, in a report sent to Twitter, “leads to a society that finds it too challenging to identify what’s true or false.”

It was the same with someone who shared true research about the efficacy of natural immunity or suggested that the virus came from a lab. It all might be factual, but it was politically inconvenient, something they called “malinformation.” In the end, out of all of these possible beliefs, they derived a 1984 binary: good and ungood.

They also applied the binary to people.

This was new. Old-school speech law punished speech, not the speaker. As a reporter I was trained that if I commit libel, if I wrote something defamatory that caused provable injury to someone, I would have to retract the error, admit it, apologize, and pay remuneration. All fair!  But the court case wouldn’t target me as a person. It wouldn’t assume that because I was wrong about X, I would also be wrong about Y, and Z.

[. . .]

One last note. As Michael and I found out recently with regard to the viral origin story, things deemed politically good often turn out to be untrue, and things deemed ungood turn out to be true.

I can recite a list if need be, but many news stories authorities were absolutely sure about yesterday later proved totally incorrect. This is another characteristic Orwell predicted: doublethink.

He defined doublethink as “the act of holding, simultaneously, two opposite, individually exclusive ideas or opinions and believing in both simultaneously and absolutely.”

Not long ago we were told in no uncertain terms the Russians blew up their own Nord Stream pipeline, that they were the only suspect. Today the U.S. government is telling us it has known since last June that Ukrainian forces planned it, with the approval of the highest military officials. But we’re not expected to say anything. We’re expected to forget.

What happens to a society that doesn’t square its mental books when it comes to facts, truth, errors, propaganda and so on? There are only a few options. Some people will do what some of us in this room have done: grow frustrated and angry, mostly in private. Others have tried to protest by frantically cataloging the past.

Most however do what’s easiest for mental survival. They learn to forget. This means living in the present only. Whatever we’re freaking out about today, let’s all do it together. Then when things change tomorrow, let’s not pause to think about the change, let’s just freak out about that new thing. The facts are dead! Long live the new facts!

We’re building a global mass culture that sees everything in black and white, fears difference, and abhors memory. It’s why people can’t read books anymore and why, when they see people like Russell who don’t fit into obvious categories, they don’t know what to do except point and shriek, like extras in Invasion of the Body Snatchers.

We have been complaining about censorship, and it’s important to do that. But they are taking aim at people in a way that will make censorship unnecessary, by building communities of human beings with no memory and monochrome perception. This is more than a speech crisis. It’s a humanity crisis. I hope we’re not too late to fix it.

Ivermectin Could Have Saved Millions of Lives, Why Was It Suppressed?

"This mass experimentation can legally be interpreted under the Nuremberg Code as a genocidal attack on humanity."

Article by Richard Gale and Dr. Gary Null.

Excerpts:

In 2004, the US Congress passed an amendment to the Federal Food, Drug and Cosmetic Act known as Emergency Use Authorization (EUA). This piece of legislature legalized an anti-regulatory pathway to allow experimental medical interventions to be expedited without proper safety evaluation in the event of bioterrorist threats and national health emergencies such as pandemics. At the time, passage of the EUA amendment made sense because it was partially in response to the 2001 anthrax attacks and the US’s entry into an age of international terrorism. However, the amendment raises some serious considerations.  Before the Covid-19 pandemic, EUAs had only been authorized on four occasions:  the 2005 avian H5N1 and 2009 H1N1 swine flu, the 2014 Ebola and the 2016 Zikra viruses.

Each of these pathogen scares proved to be false alarms that posed no threat of any pandemic proportions to Americans.  The fifth time EUAs were invoked was in 2020 during the Covid-19 pandemic, which seemed far more plausible than previous EUAs.

Before the government can authorize an EUA to deploy an experimental diagnostic product, drug or vaccine, certain requirements must be fulfilled.

First, the Secretary of the Department of Health and Human Services (HHS) must have sufficient proof that the nation is being confronted with a serious life-threatening health emergency.

Second, the drug(s) and/or vaccine(s) under consideration must have sufficient scientific evidence to suggest they will likely be effective against the medical threat.  Despite being insufficient, the evidence must at least include preclinical and observational data showing the product—diagnostic test, drug and vaccine—targets the organism, disease or condition.

Third, although the drug or vaccine does not undergo a rigorous evaluation by the FDA, it must at least show that its potential and known benefits outweigh its potential and known risks.  In addition, the product must be manufactured in complete accordance with standard quality control and safety assurances.

However, when we look back at the government’s debacles during the Covid-19 pandemic, two other EUA requirements should be spotlighted. On the one hand, an EUA cannot be authorized for any product or intervention if there is an FDA approved alternative product already available, unless the experimental product clearly shows to have a significant advantage. Moreover, and perhaps more important, EUAs demand informed consent. Every individual who receives the drug or vaccine must be thoroughly informed about its experimental status and its potential risks and benefits.  Recipients must also be properly informed about the alternatives to the experimental product and nobody should be forced to take it.

One final EUA requirement is that there must be robust safety monitoring and reporting of adverse events, injuries and deaths potentially due to the drug or vaccine. This is the responsibility not only of the private pharmaceutical manufacturers but also the FDA, physicians, hospitals, clinics and other healthcare professionals.

Obviously there are important cautions to be considered after reviewing the EUA requirements and the dangerous implications if they are not properly followed or at worse abused. Foremost are the inherent heath risks of any rapid response of experimental medical interventions, especially novel drugs and vaccines.

As we observed during the FDA approval process and roll out of Pfizer’s and Moderna’s mRNA Covid-19 jabs and J&J’s adenovirus vaccine, no long-term human trials were conducted to even estimate a reliable baseline of their relative efficacy and safety.

But perhaps equally important, the public should only place their trust in these EUA-approved experimental drugs and vaccines if their evaluation by federal health authorities is conducted in a manner that is completely transparent and takes every potential ethical challenge into consideration. However these cautions were categorically ignored and transgressed in every conceivable way. Moreover, conflicts of interests plagued the entire EUA review process.

Most egregious was that Anthony Fauci at the NIAID and other federal officials had full knowledge that other FDA-approved drugs existed that could effectively treat Covid-19 infections. The antiparasitic and antiviral drug Ivermectin best stands out.

Ivermectin was first introduced to the market in the early 1980s as an anti-parasitic drug for veterinary infections. However, its effectiveness was observed to be so remarkable and multifaceted that researchers started to investigate its potential for treating human diseases.  In 1987, the FDA approved ivermectin for treating two parasitic diseases, river blindness and stronglyoidiasis, in humans.

Since then an enormous body of medical research has grown showing ivermectin’s effectiveness for treating other diseases. Its broad range antiviral properties has shown efficacy against many RNA viruses such avian influenza, zika, dengue, HIV, West Nile, yellow fever, chikungunya and earlier severe respiratory coronaviruses. It has also been found effective against DNA viruses such as herpes, polyomavirus, circovirus-2 and others. The drug is capable of modulating a host immune response during viral infections and reduces pro-inflammatory cytokines that contribute to viral tissue damage.

Unsurprisingly, its discovers Drs. William Campbell and Satoshi Omura were awarded the 2015 Nobel Prize in Physiology and Medicine. Ivermectin was not a drug simply hidden away in a back closet; rather it has been prescribed to hundreds of millions of people worldwide. Given its decades’ long record of in vitro efficacy, it should have been self-evident for Fauci, the CDC and the WHO to rapidly conduct in vivo trials to bring ivermectin into becoming a first line of defense for early stage Covid-19 infections and for use as a safe prophylaxis. For example, if funding were devoted for the rapid development of a micro-based pulmonary delivery system, mortality rates would have been miniscule and the pandemic would have been greatly lessened. Repurposing ivermectin could have been achieved very quickly at a minor expense.

[. . .]

Early in the pandemic, physicians in other nations where treatment was less restricted, such as Spain and Italy, were sharing data with American physicians about treatments they found were effective against the SARS-2 virus.

In addition, there was a large corpus of medical research indicating that older drugs with antiviral properties could be repurposed. Doctors who started to prescribe drugs such as ivermectin and HCQ, along with Vitamin D and zinc supplementation, observed remarkable results.  Unlike the dismal recovery and high mortality rates reported in hospitals and large clinics that relied upon strict isolation, quarantine, and ventilator interventions, this small fringe group of physicians reported very few deaths among their patient loads. Even those deaths reported were more often than not compounded by patients’ comorbidities, poor medical facilities and other anomalies.

Very early into the pandemic, medical papers were showing that ivermectin was a highly effective drug to treat SARS-2 infections. In April 2020, less than a month after the WHO declared Covid-19 as a global pandemic, Australian researchers at the Peter Doherty Institute of Infection and Immunity had published their paper “The FDA- approved drug ivermectin inhibits the replication of SARS-CoV-2 virus in vitro.” Monash University’s Biomedicine Discovery Institute in Australia had also published an early study that ivermectin destroyed SARS-2 infected cell cultures by 99.8 percent within 48 hours. But no government health official paid any attention.

[. . .]

Although the EUA amendment provides some protections to authorized drug and vaccine manufacturers, it was the Public Readiness and Emergency Preparedness Act (PREP) in 2005 that expanded liability protections. In addition to protecting private corporations, PREP also shields company executives and employees from claims of personal injury or death resulting from the administration of authorized countermeasures. The only exceptions for liability are if the company or its executive offices are proven to have engaged in intentional and/or criminal misconduct with conscious disregard for the rights and safety of those taking their drugs and vaccines.

During the pandemic, the FDA issued widespread EUAs with liability immunity for the PCR diagnostic kits for SARS-2, the mRNA vaccines and anti-Covid-19 drugs such as Remdesivir, molnupiravir and Paxlovid.  Even the PCR test failed to go through a robust evaluation to determine whether it could accurately predict a SARS-2 infection. Curiously, the Secretary of the Department of Health and Human Services invoked the PREP Act on February 4, 2020 giving liability protections; this was over a month before the pandemic was officially announced, which raises serious questions about prior-planning before the viral outbreak in Wuhan, China.

From the pandemic’s outset, Fauci embarked on the media circuit to promise Americans that federal health agencies were doing everything within their means to get a vaccine on the market because there was no available drug to clear SARS-2 virus infections. As we have seen with respect to ivermectin alone, this was patently false. Rather the government placed an overriding emphasis on vaccination with a near total disregard for implementing very simple preventative measures to inhibit infections from progressing. Once mass vaccinations were underway, we were promised that the SARS-2 virus would be defeated and life would return to normal. In retrospect, we can look back and state with a degree of certainty that American health authorities and these products’ corporate manufacturers may have violated almost every EUA requirement. Everything that went wrong with the PCR kits, the experimental mRNA vaccines and novel drugs could have been avoided if the government had diligently repurposed effective and safe measures as pandemic countermeasures. Very likely, hundreds of thousands of lives would have been saved.

Shortly after the pandemic was formally announced, and with no promising treatment in sight, the FDA recommended HCQ but then quickly reversed its decision in June after Fauci publicly announced the future arrival of Gilead’s novel drug Remdesivir. The FDA’s approval of Remdesivir baffled many scientists, according to the journal Science, who were keeping a close watch on the drug’s clinical reports about a “disproportionally high number of reports of liver and kidney problems”

Similarly the FDA issued a warning statement against the use of ivermectin. Although Merck was ivermectin’s manufacturer, the company discredited its own product.  Shortly after ridiculing its drug, the Alliance for Natural Health reported, “Merck announced positive results from a clinical trial on a new drug called molnupiravir in eliminating the virus in infected patients.” Molnupiravir has a poor efficacy rate across the board including viral clearance, recovery, and hospitalizations/death (68 percent). One trial, funded by Merck, concluded the drug had no clinical benefit. More worrisome, molnupiravir was found to potentially contribute to lethal mutations in RNA viruses. The drug also has life-threatening adverse effects including mutagenic risks to human DNA and mitochondria, carcinogenic activity and embryonic death.

And still the FDA considers these novel patented drugs to be superior to ivermectin. Favoring a vaccine regime and government-controlled surveillance measures to track every American’s movements, American health officials blatantly neglected their own pandemic policies’ severe health consequences. Ineffective lockdowns, masks, social isolation, unsound critical care interventions such as relying upon ventilators, and the sole EUA approvals of the costly and insufficiently effective drugs brought about nightmares for tens of millions of adults and children. Again, the FDA worked in concert with the pharmaceutical industry to increase profit and revenues rather than improve human health and assure patient safety. This was all undertaken under Fauci’s watch and the heads of the US health agencies in direct violation of the EUA requirements to only authorize drugs and medical interventions when no other safe and effective alternative is available. As we have seen, alternatives were available and these were well known throughout the government health agencies. Instead of acting upon them and awarding EUAs to HCQ, ivermectin and other potential off-patent drugs, the government preferred to submit to their pharmaceutical masters’ demands and the financial mills that feed the CDC’s and FDA’s coffers.

The 3-year history of the pandemic highlights a sharp distinction between dependable medical research and pseudoscientific fraud.

We witnessed the CDC adopting a common Soviet era practice to redefine the very definition of a vaccine and the parameters of vaccine efficacy in order to fit their economic and ideological agendas.

This explains Washington’s frequent uninformed decisions and its aggressive public relations endeavors to silence medical opponents.  According to cardiologist Dr. Michael Goodkin’s private investigations, several of the most cited studies discrediting ivermectin’s antiviral benefits were funded by the NIH and Bill Gates and intentionally manipulated in order to produce “fake” results. These studies were widely distributed to the AMA, American College of Physicians and across mainstream media to author “hit pieces” to demonize ivermectin. The government’s belligerent and reactive diatribes, brazenly or casually advocating for censorship, were direct violations of scientific and medical integrity and contributed nothing towards developing constructive policies for handling a pandemic with a minimal cost to life. The consequence has been a less informed and grossly naïve public, which was gaslighted into believing lies.

Now that ivermectin, and to a lesser extent HCQ, have been recognized by more and more physicians as part of a first line defense to prevent and treat SARS-2 infections, we can realize that the FDA’s EUAs for the Covid-19 vaccines and novel experimental drugs were in fact an attack on the amendments and PREP directives.

Neither the vaccines nor drugs warranted emergency authorization because effective and safe alternatives were readily available. No doubt a Congressional investigation would uncover criminal misconduct, and this misconduct and conscious fraud have contributed to numerous unnecessary medically-induced injuries and deaths. Moreover, these violations of the PREP Act may have the potential to lead directly into medical crimes against humanity as outlined in the Nuremberg Code.

Between 1946 and 1947, Nazi medical doctors were tried in Nuremberg, Germany. Known as the “Doctors’ Trial”, the court found 16 of 23 doctors guilty of human experimentation that involved conducting experiments with lethal drugs and substances, sterilization, forced euthanasia and other heinous acts. These medical atrocities were conducted on some of the most vulnerable populations.

Seven Nazi doctors were executed by hanging. What became known as the Nuremberg Code after the tribunal is not a legally binding document, however it has held significant ethical and historical importance for medical research and human experimentation. The Code is regarded as a milestone in the development of international criminal law. It has informed international and domestic guidelines and regulations on human subjects, and many countries have implemented legal and ethical frameworks inspired by the Code to regulate their medical research and protect their citizens from medical abuse.

Despite serving as the baseline for modern medical ethics, it is unfortunate that no binding international treaty or declaration has been specifically initiated that directly abides by all of Nuremberg’s obligations.  Nor has the Nuremberg Code been officially adopted in its entirety as law by any nation or major medical association.

On the other hand, other international treaties, such as the Universal Declaration of Human Rights, the World Medical Association Declaration of Helsinki (which is not legally binding), the International Covenant on Civil and Political Rights (ICCPR) and the International Ethical Guidelines for Biomedical Research on Human Subjects incorporate some of Nuremberg’s main principles that aim to protect people from unethical and forced medical research.

Although the US signed the ICCPR as an intentional party, the US Senate never ratified it. The ICCPR’s Article 7 clearly states, “No one shall be subject to torture or cruel, inhuman or degrading treatment or punishment,” which can legally be interpreted to include forced medical experimentation implied as cruel, inhuman treatment. Other ICCPR articles, 6 and 17, are also applicable to medical experimentation to ensure ethical conduct, obtaining proper informed consent and the right to life and privacy. For a moment, consider the numerous senior citizens in nursing homes and hospitals who were simply administered experimental Covid-19 vaccines without full knowledge about what they were receiving. And now how many children are being coerced by the pseudoscience of health officials’ lies to be vaccinated without any knowledge of these mRNA products’ risk-benefit ratio?

International organizations, such as the United Nations, have the moral obligation to investigate violations to human rights outlined in the Nuremberg Code. Now that it has been convincingly ascertained that Pfizer and Moderna intentionally concealed their mRNA vaccine trials’ safety and efficacy data and the government repeatedly lied to the American public, it is time to hold these parties to account. Forced and mandated Covid-19 vaccination violates the Code’s demand for “voluntary consent of the human subject is absolutely essential” and the ICCPR’s prohibition that “no one shall be subjected without his free consent to medical or scientific experimentation.” Mandates to take dangerous experimental vaccines have ruined families, and livelihoods.

The US is also a signatory to the Helsinki Declaration, which, although not directly aligned with Nuremberg, shares much in common. The Declaration also shares some common features with the EUA amendment and PREP Act. These include voluntary informed consent—which is universally accepted, adequate risk and benefit information about medical interventions, and an emphasis on the principle of medical beneficence (promoting well-being and the Hippocratic rule of doing no harm). It also guarantees protections for vulnerable groups, especially pregnant women and children, which the US government and vaccine makers directly violated by conducting trials on these groups with full knowledge about these vaccines’ adverse events in adults. In addition, weighing the scientific evidence to assess the risk-benefit ratios between prescribing ivermectin and HCQ over Pfizer’s, Merck’s and Gilead’s novel experimental drugs conclusively favors the former.  This alone directly violates the ethical medical principles noted above.

However, the failure to repurpose life-saving drugs is less criminal than the motivation behind it to make room for a new generation of genetically engineered vaccines that have never before been adequately researched in human trials for long term safety.  This mass experimentation, which continues to threaten the health and well-being of millions of people, is global and can legally be interpreted under the Nuremberg Code as a genocidal attack on humanity. If the emerging data for increasing injuries and deaths due to the Covid-19 vaccines is reliable—and we believe it is—the handling of the pandemic can be regarded as the largest medical crime in human history.  In time, and with shifting political allegiances and public demands to hold our leaders in government and private industry accountable, the architects of this medical war against civilization will be brought to justice.