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

CDC Members Own More Than 50 Patents Connected to Vaccinations | LawFirms.com

CDC Members Own More Than 50 Patents Connected to Vaccinations
The CDC Immunization Safety Office is responsible for investigating the safety and effectiveness of all new vaccinations; once an investigation is considered complete, a recommendation is then made to the CDC’s Advisory Committee on Immunization Practices (ACIP) who then determines whether the new vaccine will be added to the current vaccination schedule. Members of the ACIP committee include physicians such as Dr. Paul Offit, who also serves as the chief of infectious diseases at the Children’s Hospital of Philadelphia. Offit and other CDC members own numerous patents associated with vaccinations and regularly receive funding for their research work from the very same pharmaceutical companies who manufacturer vaccinations which are ultimately sold to the public. This situation creates an obvious conflict of interest, as members of the ACIP committee benefit financially every time a new vaccination is released to the market.
— Read on www.lawfirms.com/resources/environment/environment-health/cdc-members-own-more-50-patents-connected-vaccinations

CDC and FDA ‘altered’ Covid guidance and even ‘suppressed’ findings while under political pressure, bombshell report suggests: Whistle-blower employees say they feared ‘retaliation’ if they spoke up

www.dailymail.co.uk/health/article-10759403/CDC-FDA-altered-Covid-guidance-pressure-bombshell-report-claims.html

  • Federal investigators interviewed top-level directors and managers at agencies
  • They also opened a hotline for employees to report ‘political interference’
  • Government Accountability Office uncovered widespread allegations of this
  • They raised fears that Covid guidance may have been ‘altered or suppressed’
  • GAO warned none of the agencies had systems in place for reporting allegations
  • Said they had failed to train staff in how to report and spot political interference
  • Follows allegations White House waged a war on science early in the pandemic 

CDC and FDA officials ‘altered’ Covid guidance and even ‘suppressed’ findings related to the virus due to political pressure, a bombshell report suggests.

Investigators from the watchdog Government Accountability Office (GAO) spoke to more than a dozen directors and managers who worked at the agencies behind the country’s pandemic guidance. 

They unearthed allegations of ‘political interference’ in scientific reports, raising fears that research was tampered with.

In its 37-page report, the GAO warned that neither agency had a system in place for reporting allegations of political interference. It also said they had failed to train staff how to spot and report this.

Whistleblowers said they did not speak up at the time for fear of retaliation, because they were unsure how to report the issues or believed leaders were already aware.  

This is just the latest in a growing patchwork of reports suggesting politicians influenced ‘scientific’ papers during the pandemic for their own ends.

On Tuesday, the Biden administration’s top medical adviser Dr Anthony Fauci declared the U.S. is now ‘out of the pandemic phase’ of Covid, citing low cases and hospitalizations.

But health experts were quick to question the claim — buried at the end of an interview with PBS’ NewsHour — suggesting he may have bungled his words and should only have said the nation was in a phase of ‘low hospitalizations’. 

In the early phase the White House was accused of waging a war on science, with then-president Donald Trump repeatedly pushing for Centers for Disease Control and Prevention (CDC) reports to be amended to support his views, as shown in emails made public by congressional investigators last April.

The CDC is facing allegations that it altered and suppressed Covid guidance that was meant to save lives. (Stock image of its headquarters in Atlanta, Georgia)

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The CDC is facing allegations that it altered and suppressed Covid guidance that was meant to save lives. (Stock image of its headquarters in Atlanta, Georgia) 
The FDA is facing the same accusations, following its approval of a blood plasma treatment early in the pandemic. Hospitals are no longer offering blood plasma to most patients because it provided 'little benefit'. (Stock image of their headquarters in White Oak, Maryland)

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The FDA is facing the same accusations, following its approval of a blood plasma treatment early in the pandemic. Hospitals are no longer offering blood plasma to most patients because it provided ‘little benefit’. (Stock image of their headquarters in White Oak, Maryland) 
The Biden administration's top medical advisor Dr. Anthony Fauci has declared the United States is now 'out of the pandemic phase' of Covid-19 , as cases and hospitalizations associated with the disease remain low

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The Biden administration’s top medical advisor Dr. Anthony Fauci has declared the United States is now ‘out of the pandemic phase’ of Covid-19 , as cases and hospitalizations associated with the disease remain low 

‘A few respondents from CDC and [Food and Drug Administration] FDA stated they felt that the potential political interference they observed resulted in the alteration or suppression of scientific findings,’ GAO investigators wrote in the report.

‘Some of these respondents believed that this potential political interference may have resulted in the politically motivated alteration of public health guidance or delayed publication of Covid-related scientific findings.’

The GAO report published last week looked into the two agencies, alongside the National Institutes of Health (NIH) — America’s top research institution— and the Office of the Assistant Secretary for Preparedness and Response (ASPR) — in charge of natural disaster response.

What’s All This Fuss About Snake Venom??

Stew Peters and Dr. Ardis discuss conclusions Dr. Ardis’s conclusion that Covid-19 most likely came from the King Cobra /Chinese red headed Crepes.

WORLD PREMIERE: WATCH THE WATER – TRUMP ALWAYS GAVE YOU FREEDOM OF CHOICE

Situation Update
April 14, 2022

Video – WORLD PREMIERE: WATCH THE WATER – TRUMP ALWAYS GAVE YOU FREEDOM OF CHOICE: https://rumble.com/v10x9dt-world-premiere-watch-the-water-trump-always-gave-you-freedom-of-choice.html

FULL VIDEO: https://rumble.com/v10uh1l-situation-update-41322-venomtech-company-announces-massive-library….html

For more Situation Updates: https://rumble.com/c/SituationUpdate

WATCH: Connecting the CIA TO COBRA VENOM!!!!!!!! 1975 NY TIMES ARTICLE: https://rumble.com/v10zb8z-ny-times-1975-publication-cia-using-cobra-venom

Dr. Ardis Live Q&A: COVID, Snake Venom, and Our Water Supply

Man in America April 14, 2022

Dr. Ardis’ website: https://thedrardisshow.com/

After Dr. Ardis’ bombshell interview with Stew Peters, everyone wants to know—is he crazy, a heroic whistleblower, or just a humble man trying to share the COVID science he uncovered? Is there any truth to the claims that snake venom and COVID are linked? Today, Seth gives you the chance to ask Dr. Ardis your questions for yourself. Join us for a live Q&A

WATCH: https://rumble.com/v10yvn1-dr.-ardis-live-q-and-a-covid-snake-venom-and-our-water-supply.html

FOR MORE VIDEOS And Interviews with DR. Ardis about SNAKE VENOM, go here

CDC to extend federal transportation mask mandate for additional 15 days

CDC to extend federal transportation mask mandate for additional 15 days

By Brenda Goodman and Betsy Klein, CNN

Updated 11:42 AM ET, Wed April 13, 2022

A traveler walks through the George Bush Intercontinental Airport on December 03, 2021 in Houston, Texas.
A traveler walks through the George Bush Intercontinental Airport on December 03, 2021 in Houston, Texas.

HERE WE GO AGAIN…

The corrupt Genocide CDC, Plandemic-Pusher’s, are at it again… as always… using any excuse they can, whether it makes sense or whether science agrees or not have come to another nefarious conclusion about masks mandates.

Here’s the kicker… their heinous excuse this time is to gather more information and understanding of the BA.2 variant of the coronavirus.

Can someone please explain this to me?

Here’s the article:

The US Centers for Disease Control and Prevention plans to extend the federal transportation mask mandate for another 15 days to early May, according to a Biden administration official familiar with the decision.

The announcement is expected as early as Wednesday afternoon from the CDC. The mandate is now set to expire on May 3. The Associated Press was first to report the extension.

The administration official familiar with the decision told CNN the goal of the extension was to gather more information and understanding of the BA.2 variant of the coronavirus.

“Since early April, there have been increases in the 7-day moving average of cases in the US. In order to assess the potential impact, the rise of cases has on severe disease, including hospitalizations and deaths, and health care system capacity, CDC is recommending that TSA extend the security directive to enforce mask use on public transportation and transportation hubs for 15 days, through May 3, 2022,” the official told CNN.

The official added, “This will give additional time for the CDC to learn more about BA.2 and make a best-informed decision.”

The US is now averaging 38,345 new Covid-19 cases per day, according to data from Johns Hopkins University. Cases are trending up in more than half of states — including all but one state in the Northeast, Delaware. But the daily rate is still one of the lowest since mid-July.

According to the latest estimates from the CDC, BA.2 caused 86% of new Covid-19 cases nationwide last week.

The mandate , which requires masks on public transportation such as planes, trains, buses — as well as in hubs like airports and bus terminalshad been set to expire on April 18. White House Covid-19 Response Coordinator Dr. Ashish Jha told CNN on Monday that the CDC planned to share a scientific framework this week for the federal transportation mask mandate.

This is a breaking story and will be updated. Source: (CNN)

Now that we have the masks thing cleared up go the next two weeks at least let me take this to another level.

if you’re one of those who’s thinking hasn’t quite caught up with some of your relatives, friends or coworkers or the rest of us, I would really like you to consider adjusting your thinking “outside the box” a little bit for a moment because you deserve to know and understand the truth like the rest of us. If society as a whole doesn’t start to grasp the entire truth of what has been happening and has happened, things are not going to turn out very well for any of us. This much I am convinced.

In case you missed it!

Just in case you missed the “venomous” conclusion regarding the origin of the coronavirus you might want to hear the latest findings. I was blown away! Videos discussion’s centered around the research findings of Dr. Bryan Ardis (www.ardisantidote.com), the real origin of the virus, the goal of this Plandemic, and who is behind it!

The plandemic continues, but its origins are still a nefarious mystery. How did the world get sick, how did Covid really spread, and did the Satanic elite tell the world about this bioweapon ahead of time? Dr. Bryan Ardis (www.ardisantidote.com) has unveiled a shocking connection between this pandemic and the eternal battle of good and evil which began in the Garden of Eden.

Here’s a couple of recommended watches for you. Be sure you’re sitting down! I literally watched one of them 3 times last night because I couldn’t believe my ears!

#1 Watch

Watch the Water with Stew Peters: https://rumble.com/v10mnew-live-world-premiere-watch-the-water.html

In this Stew Peters Network exclusive, Director Stew Peters, award winning filmmaker Nicholas Stumphauzer and Executive Producer Lauren Witzke bring to light a truth satan himself has fought to suppress.

For more information on Dr. Bryan Ardis: Visit http://ardisantidote.com/ to learn how to protect you and your loved ones during this biological war.

# 2 Watch

4.13.22: VENOM, COBRAS, Digital Warriors, NYC…more EXPOSURE of the [DS} evil! PRAY!– with And We Know

https://rumble.com/v10u04f-4.13.22-venom-cobras-digital-warriors-nyc…more-exposure-of-the-ds-evil-pr.html

CDC reports fewer COVID-19 pediatric deaths after data correction

The U.S. Centers for Disease Control and Prevention reported 966,575 deaths from COVID-19 on Friday after it corrected the data earlier this week, which reduced the death tallies in all age-groups, including children.

The health agency, in a statement to Reuters, said it made adjustments to its COVID Data Tracker’s mortality data on March 14 because its algorithm was accidentally counting deaths that were not COVID-19-related.

The adjustment resulted in removal of 72,277 deaths previously reported across 26 states, including 416 pediatric deaths, CDC said.

The reduction cut the CDC’s estimate of deaths in children by 24% to 1,341 as of March 18.
— Read on news.yahoo.com/cdc-reports-fewer-covid-19-204027980.html

Kakistocracy: noun, government by the worst persons; a form of government in which the worst persons are in power

Kakistocracy: noun, government by the worst persons; a form of government in which the worst persons are in power.

The old saying goes that even a blind squirrel finds a nut occasionally.  So you might think that during a 50-year political career, the odds would dictate that Joe Biden would, once in a blue moon, make a correct decision — just based on the odds.  But you’d be mistaken.  Biden has stumbled and bumbled from one disastrous decision to the next.  Disastrous, that is, for America.  Biden himself has prospered handsomely in spite of his glaring incompetence and corruption. 

Biden’s long Senate career was based on being the credit card companies’ man in Washington.  While crowing endlessly about the working class being “his people,” Biden sponsored bills allowing bank issuers to charge egregious interest rates and to make it harder for working men to escape the credit trap through bankruptcy.

When Biden chaired the Senate Judiciary Committee, he turned the confirmation of Clarence Thomas into a political smear campaign that descended into a degenerate three-ring circus. In his first campaign for president, he failed to garner a single percentage point before having to withdraw when confronted with his past lies and blatant plagiarism. He literally stole a speech detailing a British politician’s life story. He ran again in 2008 but again failed to reach even one percent of the vote.

When Barack Obama took him off the primary trash heap to make him vice president, Biden first made a hash out of the 2009 American Recovery and Reinvestment Act, wasting hundreds of billions on boondoggles and giveaways to Democrat cronies. Little of the recovery billions was spent on anything useful to America. Biden went on to manage our relations with China and Ukraine, pocketing untold millions for himself and his family by selling out America’s security interests.

By the time he ran for president again in 2020 he was a spent husk of his former corrupt and incompetent self, delivering asinine performances in the Iowa caucus and New Hampshire primary. When the Democrat establishment propped him up to once again stop Bernie Sanders, Biden was set up for the strangest presidential campaign in modern history. While Donald Trump barnstormed the nation with packed, enthusiastic rallies, Biden cowered in his basement, occasionally venturing out to speak with a few dozen voters sitting in circles drawn on the floor.

For his vice presidential pick, he chose — if you can believe it — an even more buffoonish candidate than himself.

Had it not been for Mark Zuckerberg buying and staffing government election offices in swing states, and the media and Big Tech’s censorship of the Biden family’s corruption, Biden would now be enjoying his dotage in Delaware, creeping on unsuspecting children with yarns of Corn Pop and South African arrests.

Instead, the man with one of the most astonishing records of abject failure in Washington was installed in the White House, and he has remained true to form.  As one of a hundred senators and then as vice president, there was a limit to how much damage he could do.  But as president, the shackles have been removed.

His first agenda item was to throttle our oil and gas sector, offshoring tens of thousands of good paying jobs to Russia and the Middle East — along with our energy independence. He threw open our southern border and encouraged virtually unlimited illegal immigration — during a global pandemic.

He sponsored trillions of dollars in wasteful spending, pushing our national debt to over $31 trillion.  Were it not for two Democrat senators who had not yet taken leave of their senses, it would have been even worse.  As it is, Biden has sparked the largest one-year increase in inflation in 40 years.

Biden’s “defund the police” rhetoric delivered us soaring violent crime in Democrat-run cities, while he sicced federal law enforcement on parents who object too strenuously to their children being indoctrinated with anti-White racism and LGBTQIA+ ideology. 

It can truly be said that as president, Biden’s record of failure remains unblemished.  

But now comes what may be the capstone on Biden’s long history of buffoonery and corruption.  In Ukraine, we have an armed conflict that threatens to plunge the world into an economic depression and raises the specter of nuclear war.  Not only did Biden set the stage for this calamity when, as vice president, he was in charge of Ukraine policy and led Kiev to believe that NATO membership was in Ukraine’s future, but on the eve of the Russian invasion, he refused to admit that it was not.  Then Biden all but admitted to Vladimir Putin — on live TV, no less — that NATO would not defend Ukraine if Russia chose to invade. 

In the aftermath of Russia’s invasion, Biden and his administration have crafted sanctions that seem almost designed to boomerang on America’s and Europe’s fragile post-pandemic economies, while forcing Russia into a deeper alliance with China

With the U.S. over $31 trillion in debt, Biden seems totally oblivious to the perilous position of the U.S. dollar as the world’s reserve currency and the consequences should that privileged position end. 

Economists predict that food and gasoline will cost the average U.S. household an additional $3,000 this year, and inflation threatens to push millions of lower-middle income-earners into abject poverty.

And bumbling, corrupt Joe Biden isn’t yet halfway through his first — and please God, last — term.

Image: Gage Skidmore via Flickr, CC BY-SA 2.0.
Image: Gage Skidmore via Flickr, CC BY-SA 2.0.

Image: Gage Skidmore via Flickr, CC BY-SA 2.0.

Jim Daws is a recovering talk radio host at jimdaws.com.

Every plandemic criminal deserves swift and merciless punishment for their crimes against humanity. Every plandemic criminal deserves swift and merciless punishment for their crimes against humanity and Collins all conspired to commit mass murder with the plandemic: Dr. Naomi Wolf

Fauci, Walensky and Collins all conspired to commit mass murder with the plandemic: Dr. Naomi Wolf – NaturalNews.com
— Read on www.naturalnews.com/2022-03-08-fauci-walensky-collins-conspired-mass-murder-plandemic.html

Fauci, Walensky and Collins all conspired to commit mass murder with the plandemic: Dr. Naomi Wolf

Image: Fauci, Walensky and Collins all conspired to commit mass murder with the plandemic: Dr. Naomi Wolf

(Natural News) During a recent appearance on Steve Bannon’s “War Room: Pandemic” program, Dr. Naomi Wolf fired a shot against those who perpetrated the Wuhan coronavirus (COVID-19) plandemic, accusing them of conspiring to commit mass murder.

Wolf named Tony Fauci from the National Institute of Allergy and Infectious Diseases (NIAID), Rochelle Walensky from the Centers for Disease Control and Prevention (CDC), and Francis Collins of the National Institutes of Health (NIH) as co-conspirators in the genocide campaign.

“What is the crime of murder? And it’s different state by state, but, you know conspiracy to commit murder is pretty loosely defined in California penal code 182, for instance,” Wolf told Bannon. “And now that we’ve seen the Pfizer documents, there are nine pages of harms, all the adverse effects.”

“The fact that people like Rochelle Walensky, Dr. Fauci, Dr. Collins – all the ‘influencers’ who were paid, as we now know, said ‘safe and effective,’ this needs criminal charges. This could be conspiracy to murder. And members of the media could also be accessories to murder.”

Be sure to watch the below clip of Wolf speaking:

Every plandemic criminal deserves swift and merciless punishment for their crimes against humanity

These are some pretty big words, though Wolf failed to mention Donald Trump, who signed the PREP Act and launched Operation Warp Speed, which has injured and killed millions.

At least she is drawing attention to the need for justice, though, and perhaps eventually the whole thing will unravel exposing all of the vermin involved with this mass depopulation campaign.

Even if Fauci, for instance, is suddenly out of the news cycle, people have not forgotten what this decrepit Josef Mengele wannabe did to the world, terrorizing it for two years with mask and “vaccine” mandates.

Then we have Walensky, whose husband raked in millions from the plandemic scam.

Back in January, Wolf spoke out against Fauci and the others, accusing them of “premeditated manslaughter” against “millions of people.”

Keep in mind that Wolf used to advise Bill Clinton, which makes her an unlikely candidate to be saying these types of things, especially publicly.

“The fact that Dr. Fauci grossly perjured himself is hugely apparent,” Wolf said at the time about how Fauci repeatedly lied before Congress about gain of function research and other things.

“It is the least of the crimes if indeed these are verified documents. I can’t overstate this. This is a premeditated kind of manslaughter of millions of people coordinated at the highest levels according to these documents. Treatments that would have saved lives were intentionally or reportedly intentionally suppressed.”

Apparently this was not just rhetoric for Wolf, who has continued to press forward in the pursuit of justice against all involved with pushing plandemic tyranny and mass genocide on not just Americans but most of the world.

“Everyone involved in pushing these injections should be charged with manslaughter at the very least,” wrote someone on Twitter. “But as they already knew they were highly toxic and lethal, murder is the correct charge.”

“There has been a lot of bad that has happened because Trump didn’t confiscate the Dominion Voting machines and force the DOJ to do its job and prosecute the massive election fraud,” pointed out someone else at Citizen Free Press about how Trump’s failures, whether they were deliberate or not, paved the way for all of this to happen under his watch.

The latest plandemic-related news can be found at Pandemic.news.

Sources include:

Twitter.com

NaturalNews.com 1

NaturalNews.com 2

NaturalNews.com 3

CitizenFreePress.com

A lavender spray was supposed to freshen homes. Instead, it killed two people.

A months-long CDC investigation revealed an aromatherapy spray imported from India and sold at Walmart was contaminated with deadly bacteria.

On July 12, a 5-year-old boy in Georgia arrived at an emergency department following several days of sickness. He’d been vomiting, was weak and had a sore throat. His heart rate was unusually fast. His fever spiked to more than 102 degrees.

Doctors admitted the child to the hospital to keep an eye on him and help keep him properly hydrated. That night, his breathing became labored, and he tested positive for Covid-19.

Doctors immediately started a typical treatment for the infection, including steroids and an antiviral drug called remdesivir. 

He did not get better. Within four days of hospitalization, he died. 

An autopsy later detected the coronavirus in his lungs and upper airways. But it also showed something surprising: bacteria called Burkholderia pseudomallei in the boy’s lungs, liver, spleen and brain.

That finding would eventually lead investigators to solve three other cases of Burkholderia pseudomallei infection that occurred earlier in the year in three different states. Details of all four cases were published Wednesday in the New England Journal of Medicine.

Solving a microscopic mystery

The bacteria Burkholderia pseudomallei are almost never found in the United States; rather, they’re generally found in contaminated soil or water in parts of South and Southeast Asia. 

But the boy’s family said they had not traveled outside of the country. Samples taken from the family’s water supply and soil outside the home turned up nothing.

Burkholderia pseudomallei can also be aerosolized and inhaled, so investigators tested products inside the boy’s home. 

It was an “arduous investigation,” said study co-author Julia Petras, an epidemic intelligence service officer with the Centers for Disease Control and Prevention. Over the course of several months, investigators took dozens of samples from products in the boy’s home, she said. 

Three months later, in October, investigators discovered the bacteria in an aromatherapy room spray in the house. The product, the lavender and chamomile scent of Better Homes & Gardens Essential Oil Infused Aromatherapy Room Spray With Gemstones, had been imported from India and sold at 55 Walmart stores, as well as on Walmart’s website.

“When we first got the confirmation, it came as a huge relief to us,” Petras said.

The discovery of the bacteria in the aromatherapy product helped investigators solve the three other cases of Burkholderia pseudomallei infection that had occurred earlier in the year. Each of those patients were found to have the same specific strain of the bacteria found in the spray bottle, suggesting they had also used the contaminated product.

The cases were first made public in October, when the CDC issued an alert about the aromatherapy spray and the Consumer Product Safety Commission announced that Walmart was recalling nearly 4,000 bottles of the product, as well as five other scents under the same product name: lemon and mandarin; lavender; peppermint; lime and eucalyptus; and sandalwood and vanilla.

A difficult diagnosis

Burkholderia pseudomallei cause an illness called melioidosis. It’s treatable with certain intravenous antibiotics if caught early.

But because the bacteria are so rare in the U.S., signs of melioidosis can be mistaken for other respiratory illnesses, such as the flu, Covid or even tuberculosis.

All four patients whose cases are detailed in the new report initially had a wide range of vague symptoms, such as fatigue, shortness of breath, fever and nausea.

One case involved a 4-year-old girl in Texas whose family sought medical attention for her several times after she’d been vomiting and had a fever of more than 103 degrees. Investigators later confirmed her family had the aromatherapy spray product in the house.

Doctors thought perhaps the girl had a urinary tract infection and put her on a variety of antibiotics. Within days, she was hospitalized with septic shock, which causes dangerously low blood pressure and organs to shut down.

The girl survived. But three months after leaving the hospital, the girl still needed to use a wheelchair and was nonverbal, the study authors wrote.

The families of both the young girl and the boy told investigators that they had sometimes used the spray on pillows and bedding, Petras said.

The other two patients were adults, both 53 years old. A man living in Minnesota went into the hospital with weakness and confusion. His fever later soared to 104 degrees, and he had severe pain in one of his hips.

He was later discharged, but his mental status had not improved at that time.

And a woman in Kansas who was hospitalized with breathing problems and weakness later went into septic shock. She died nine days later.

Melioidosis can occur through normal use of contaminated air fresheners and other room sprays, said Dr. Jill Weatherhead, an assistant professor of tropical medicine and infectious diseases at the Baylor College of Medicine in Houston. 

“We know you can get this infection through inhalation into the lungs,” Weatherhead, who was not involved in the CDC investigation, said. “Unfortunately in this case, the bacteria was already being aerosolized. If you breathe that in, it will cause disease.”

Source: www.nbcnews.com/nightly-news/video/cdc-says-aromatherapy-spray-may-be-linked-to-deadly-infection-124402757653

It’s The Biggest FDA Scandal In History: Interview With Whistleblower Linda Martin, Ph.D.

It’s The Biggest FDA Scandal In History: Interview With Whistleblower Linda Martin, Ph.D.

Speaking About News

Got Science? Are you sure?

Dr. Brian Hooker invites some of the leading voices in science and medicine to break down the studies and weigh in on the controversies so the rest of us have an opportunity to understand the science that drives public health policy and medical progress. Watch at link Below:

‘Doctors And Scientists’ With Brian Hooker, PHD. – CHD TV: Livestreaming Video & Audio (childrenshealthdefense.org)

CDC Has Not Been Transparent With the American Public on COVID

An article published this past weekend in The New York Times highlights a glaring problem with the U.S. Centers for Disease Control and Prevention (CDC) and its policy recommendations related to the pandemic during the past two years. The problem has to do with lack of transparency regarding hospitalizations for COVID-19 and the effectiveness of vaccinations for the illness.1 2 The Times article, written by Apoorva Mandavilli, starts out:

For more than a year, the Centers for Disease Control and Prevention has collected data on hospitalizations for Covid-19 in the United States and broken it down by age, race and vaccination status. But it has not made most of the information public. When the C.D.C. published the first significant data on the effectiveness of boosters in adults younger than 65 two weeks ago, it left out the numbers for a huge portion of that population: 18- to 49-year-olds…1 3

The article continues:

Two full years into the pandemic, the agency leading the country’s response to the public health emergency has published only a tiny fraction of the data it has collected, several people familiar with the data said.

The CDC has shared only a “tiny fraction” of its COVID data with the American public?

Former CDC Director Thinks Agency Should Let COVID Data Speak for Itself

According to CDC spokesperson, Kristen Nordlund, one of the reasons for the lack of data transparency is because “basically, at the end of the day, [the data is] not yet ready for prime time,” noting that the CDC’s “priority when gathering any data is to ensure that it’s accurate and actionable.”1 In an interview with Fox News, former CDC director Robert Redfield, MD confirmed this view, saying…

One of the things is that CDC has a tendency to look at data and make sure that they believe that data is accurate. They call it curating the data. So very frequently the data is out of sync to be able to be in real-time to respond.4

But Dr. Redfield suggested that he disagreed with this practice. He said that he believes whatever data the CDC collects should “absolutely get out there in real-time.” He added:

I think the best thing for CDC to do is to tell the American public the truth and let the data there. I’m sure the American public is intelligent enough to understand the explanations. I know there’s a concern that they have that the data may somehow be misinterpreted to determine the efficacy of the vaccines, rather than just tell people the truth.4

CDC Reluctance to Track COVID “Breakthrough Cases” Due to Fear of Contributing to Vaccine Hesitancy

Nordlund reportedly said that another reason for the CDC’s hesitancy to be more transparent was due to fear that its data might be misinterpreted–that information about the number of fully vaccinated people “breakthrough” SARS-CoV-2 infections, for example, could lead to concerns about the effectiveness of the COVID shots.1 2

Epidemiologist Jessica Malaty Rivera, MS, who was a member of the team that ran The COVID Tracking Project,5 dismissed the CDC worries about incomplete data being misinterpreted. She said, “We are at a much greater risk of misinterpreting the data with data vacuums, than sharing the data with proper science, communication and caveats.”

During the past two years, the CDC has frequently been criticized for its COVID and COVID vaccine data collection practices, its mixed and confusing messaging and a growing perception that the agency has not been fully transparent with the American public regarding the pandemic.6 7 8 9 10 11 12 13 14 15 16

Perhaps one of the clearest examples of the CDC’s failure to provide timely and accurate COVID-related information is the agency’s inability or unwillingness to adequately track the number of cases in which fully vaccinated (and boosted) individuals have tested positive for SARS-CoV-2. Because of this, it is not known how many “breakthrough cases” there have been in the United States. Consequently, there is no way to know for sure how effective the COVID shots have been in preventing the spread of the SARS-CoV-2 virus and COVID illness.

This represents a huge and fundamental scientific knowledge gap underlying the primary tool the U.S. government has aggressively pushed on the American people to deal with COVID. But this is only part of the problem. That other part has to do with the lack of reliable information regarding the number of people in the U.S. who have been hospitalized with COVID.

In April 2021, the CDC arbitrarily decided to stop tracking coronavirus breakthrough cases so that it could focus on tracking only breakthrough cases that resulted in hospitalization or death. The assumption was that this major change in policy would allow the agency to more accurately gauge the number of vaccinated people being hospitalized for COVID and, by extension, the overall number of people hospitalized for the illness.12

CDC System for Tracking COVID Hospitalizations in Need of Overhaul

But it has recently come to light that the system the CDC has been using to count COVID hospitalizations is deeply flawed. According to an article in Politico on Feb. 7, 2021 titled “Biden officials trying to recalculate U.S. Covid-19 hospitalizations,” the U.S. government has established a task force to work with “hospitals nationwide to improve COVID-19 reporting.” The task force wants hospitals to report the number of patients who are hospitalized because they have COVID and separate those from the patients who are hospitalized for other reasons but test positive for the SARS-CoV-2 virus after being admitted.17 18

As reported by The Vaccine Reaction earlier this month:

What this suggests is that, in the past, U.S. hospitals have been counting people hospitalized for reasons other than COVID as COVID patients if they happened to test positive for SARS-CoV-2 after admission. This would have the effect of increasing hospital COVID case counts, making the effects of COVID on U.S. hospitals appear worse than they actually were. Remember all those media reports about how overwhelmed hospitals were with COVID patients? It now appears that at least some of that reporting may have been inaccurate, even grossly inaccurate.18

So not only do we not know how effective the COVID shots have been in real-world circumstances, we do not know how many vaccinated (or unvaccinated) people have been hospitalized for COVID–which means that we really do not know how many people have actually died of COVID, in general. It is no wonder the CDC has consistently found it so difficult to be forthcoming.


References

1 Mandavilli A. The C.D.C. Isn’t Publishing Large Portions of the Covid Data It CollectsThe New York Times Feb. 20, 2022.

2 Rumpf S. CDC Under New Scrutiny For Collecting Wide Variety of Covid-Related Data But Publishing ‘Only a Tiny Fraction’MSN Feb. 20, 2022.

3 Mandavilli A. Younger Americans Benefited Less From Booster Shots Than Older PeopleThe New York Times Feb. 4, 2022.

4 Fox News. CDC reportedly published ‘tiny fraction’ of COVID data. Feb. 21, 2022.

5 The COVID Tracking Project. Mar. 7, 2021.

6 Abutaleb Y, Sun LH. How CDC data problems put the U.S. behind on the delta variantThe Washington Post Aug. 19, 2021.

7 Feldmann L. The trouble with transparency: How pandemic is challenging the CDCThe Christian Science Monitor Aug. 5, 2021.

8 Fox M. Analysis: CDC fails to publish data needed to judge risk of breakthrough infection CNN July 28, 2021.

9 Pollard MS, Davis LM. Decline in Trust in the Centers for Disease Control and Prevention During the COVID-19 Pandemic. RAND 2021.

10 Simmons-Duffin S. CDC is criticized for failing to communicate, promises to do better. NPR Jan. 7, 2022.

12 Cáceres M. CDC Intentionally Undercounting COVID-19 “Breakthrough Cases” in Vaccinated PersonsThe Vaccine Reaction May 23, 2021.

13 CBSN. CDC Lacking Data on Breakthrough COVID-19 InfectionsThe Vaccine Reaction Sept. 6, 2021.

14 CNVC. CDC Pressured to Track Breakthrough COVID Cases Among the VaccinatedThe Vaccine Reaction July 26, 2021.

15 Miltimore J. What is the True Vaccine Breakthrough Rate? The CDC Doesn’t Want You to KnowThe Vaccine Reaction Oct. 11, 2021.

16 Putka S. CDC Hasn’t Updated COVID Vax Breakthrough DataMedPage Today Nov. 11, 2021.

17 Banco E. Biden officials trying to recalculate U.S. Covid-19 hospitalizationsPolitico Feb. 7, 2022.

18 Cáceres M. U.S. Hospitals May ‘Recalculate’ How They Report COVID Cases. The Vaccine Reaction Feb. 13, 2022.

Original post from https://speakingaboutnews.com/its-the-biggest-fda-scandal-in-history-interview-with-whistleblower-linda-martin-ph-d/