- Dr. Robert Malone invented the mRNA and DNA vaccine core platform technology. He has grave concerns about the lack of transparency of side effects, censoring of discussion and the lack of informed consent that these bring
- Free SARS-CoV-2 spike protein is biologically active — contrary to initial assumptions — and causes severe problems. It is responsible for the most severe effects seen in COVID-19, such as bleeding disorders, blood clots throughout the body and heart problems. These are the same problems we now see in a staggering number of people who have received the COVID-19 “vaccine”
- The spike protein also has reproductive toxicity, and Pfizer’s biodistribution data show it accumulates in women’s ovaries. Data suggests the miscarriage rate among women who get the COVID “vaccine” within the first 20 weeks of pregnancy is 82%
- Israeli data show boys and men between the ages of 16 and 24 who have been vaccinated have 25 times the rate of myocarditis (heart inflammation) than normal
- The COVID-19 injections have emergency use authorization only, which can only be granted if there are no safe and effective remedies available. Such remedies do exist, but have been actively censored and suppressed
In the video above, DarkHorse podcast host Bret Weinstein, Ph.D., an evolutionary biologist, interviews Dr. Robert Malone, the inventor of the mRNA and DNA vaccine core platform technology,1 and Steve Kirsch, an entrepreneur who has been researching adverse reactions to COVID-19 gene therapies.
I realize that this is an absolutely epic three-hour interview but if you ever valued what I have been teaching, you must at a bare minimum very carefully read this entire article.
Malone is the scientist that actually invented the technology that makes the COVID jab possible and he spills the beans on just how this introduction has been ethically compromised to make informed consent absolutely impossible for the average person. Watch the interview if your schedule allows, but carefully read this article for sure.
Kirsch recently published the article, “Should You Get Vaccinated?” in which he reviews how and why he has changed his mind about the COVID-19 “vaccines.” This after he got both doses of the Moderna shot, as have his three daughters.
If you or someone you know is equivocal about the COVID jab, then please, you simply MUST read Kirsh’s article as it is clearly one of the best pieces written on the topic and provides the other side of the story that is NEVER given in the mainstream media. Remember, without full disclosure of the vaccine’s risk, it is impossible to have informed consent.2 If you read Kirsch’s article, you will get, in great detail, the other side that the conventional media refuses to share. He writes:
“I recently learned that these vaccines have likely killed over 25,800 Americans (which I confirmed 3 different ways) and disabled at least 1,000,000 more. And we’re only halfway to the finish line. We need to PAUSE these vaccines NOW before more people are killed.
Based on what I now know about the miniscule vaccine benefits (approximately a 0.3% reduction in absolute risk), side effects (including death), current COVID rates, and the success rate of early treatment protocols, the answer I would give today to anyone asking me for advice as to whether to take any of the current vaccines would be, ‘Just say NO.’
The current vaccines are particularly contraindicated if you have already been infected with COVID or are under age 20. For these people, I would say ‘NO! NO! NO!’
In this article, I will explain what I have learned since I was vaccinated that totally changed my mind. You will learn how these vaccines work and the shortcuts that led to the mistakes that were made.
You will understand why there are so many side effects and why these are so varied and why they usually happen within 30 days of vaccination. You will understand why kids are having heart issues (for which there is no treatment), and temporarily losing their sight, and ability to talk. You will understand why as many as 3% may be severely disabled by the vaccine.”
The Spike Protein Is a Bioactive Cytotoxin
As explained by Malone, many months ago he warned the U.S. Food and Drug Administration that the spike protein — which the COVID-19 “vaccines” instruct your cells to make — could be dangerous. The FDA dismissed his concerns, saying they did not believe the spike protein was biologically active. Besides, the vaccine makers specifically designed the injections so that the spike protein would stick and not float about freely.
Well, they were wrong on both accounts. It’s since been well-established that, indeed, the SARS-CoV-2 spike protein gets free, and that it is biologically active and causes severe problems. It is responsible for the most severe effects seen in COVID-19, such as bleeding disorders, blood clots throughout the body and heart problems.
These are the same problems we now see in a staggering number of people having received one or two shots of COVID-19 “vaccine.” For more in-depth information about how the spike protein causes these problems, please see my interview with Stephanie Seneff, Ph.D., and Judy Mikovits, Ph.D.
Using the word vaccine isn’t really appropriate here, and I don’t want to contribute to the misuse of that word. These injections are clearly not vaccines. They don’t work like any previous conventional vaccines. As the actual inventor of the mRNA vaccines clearly says in the interview, they are gene therapy. So, please understand that when I say vaccine or vaccination, I’m really talking about gene therapy.
Spike Protein Disseminates Throughout Your Body
In a recent interview3 with Alex Pierson, Canadian immunologist and vaccine researcher Byram Bridle, Ph.D., discussed previously unseen research obtained from the Japanese regulatory agency through a freedom of information act request.
The study was a biodistribution study done by Pfizer, which showed that the mRNA in the vaccine does not stay in and around the vaccination site but is widely distributed in the body, as is the spike protein.4
This is a serious problem, as the spike protein is a toxin shown to cause cardiovascular and neurological damage. Once in your blood circulation, the spike protein binds to platelet receptors and the cells that line your blood vessels. When that happens, it can cause platelets to clump together, resulting in blood clots, and/or cause abnormal bleeding. I detailed these and other findings in “Researcher: ‘We Made a Big Mistake’ on COVID-19 Vaccine.”
Dangerous Corners Were Cut
The spike protein also has reproductive toxicity, and Pfizer’s biodistribution data show it accumulates in women’s ovaries. Kirsch cites data suggesting the miscarriage rate among women who get the COVID “vaccine” within the first 20 weeks of pregnancy is 82%.5 The normal rate is 10%, so this is no minor uptick. Kirsch writes:6
“It is baffling that the CDC says the vaccine is safe for pregnant women when it is so clear that this is not the case. For example, one our family friends is a victim of this. She miscarried at 25 weeks … She had her first shot 7 weeks ago, and her second shot 4 weeks ago.
The baby had severe bleeding of the brain and other disfigurements. Her gynecologist had never seen anything like that before in her life. They called in a specialist who said it was probably a genetic defect (because everyone buys into the narrative that the vaccine is safe it is always ruled out as a possible cause).
No VAERS report. No CDC report. Yet the doctors I’ve talked to say that it is over 99% certain it was the vaccine. The family doesn’t want an autopsy for fear that their daughter will find out it was the vaccine. This is a perfect example of how these horrible side effects just never get reported anywhere.”
Disturbingly, the Pfizer biodistribution data package reveals that corners were cut in the interest of speed, and one of the research facets that were skipped was reproductive toxicology. Yet, despite the lack of an initial reproductive toxicology investigation and a rapidly growing number of reports of miscarriages (which is likely to be a significant undercount), the Centers for Disease Control and Prevention is still urging pregnant women to get vaccinated. Why is that?
Is There Purposeful Suppression of VAERS Data?
What’s more, as discussed in the interview, there’s evidence that data in the Vaccine Adverse Event Reporting System (VAERS) is being manipulated as reports that were filed are now missing. Why were they removed? And without the filers’ consent?
Even with that manipulation, the number of deaths reported post-vaccination against COVID-19 is beyond anything we’ve ever seen. According to Kirsch, the rate of death from COVID-19 shots exceeds that of more than 70 vaccines combined over the past 30 years, and it’s about 500 times deadlier than the seasonal flu vaccine,7 which historically has been the most hazardous.
Other serious effects are also off the charts. For example, Israeli data show boys and men between the ages of 16 and 24 who have been vaccinated have 25 times the rate of myocarditis (heart inflammation) than normal.8 Additionally, many young people are actually dying as a result of this myocarditis.9
Malone points out that, in re-reading the most current version of the Emergency Use Authorization (EUA) that governs these COVID shots, he discovered that the FDA opted not to require stringent post-vaccination data collection and evaluation, even though they had the latitude to do so.
As noted by Weinstein, this is yet another anomaly that needs an answer. Why did they opt for such lax data capture, because without it, there’s no way of evaluating the safety of these products. You cannot identify the danger signals if you don’t have a process for capturing effects data and evaluating all of it.
“The whole logic of EUA is you’re basically substituting real-time capture of key information for prospective capture of key information,” Malone explains. “But to do that, you’ve got to get the information and it has to be rigorous.”
Furthermore, as noted by Weinstein, if you release a vaccine under emergency use — because you say there’s an unprecedented health emergency and there are no other options, therefore it’s worth taking a larger than normal risk — then you still would not give it to people who are at no or low risk of the disease in question.
This would include children, teens and healthy individuals under the age of 40, at bare minimum. Children appear naturally immune against COVID-1910 and have been shown to not be disease vectors,11 and people under 40 have an infection fatality ratio of just 0.01%.12 That means their chances of survival is 99.99%, which is about as good as it gets.
Pregnant women would also be excluded as they are a high-risk category for any experimentation, and anyone who has recovered from COVID would be excluded as they now have natural immunity and have no need for a vaccine whatsoever. In fact, a recent Cleveland Clinic study13,14 found people who had tested positive for SARS-CoV-2 at least 42 days prior to vaccination reaped no additional benefit from the jabs.
Yet all of these incredibly low-risk groups are urged and even inappropriately incentivized to get vaccinated, and this too is anomalous behavior. Part of the risk-benefit analysis is not only the risk of serious outcomes and death from the disease, but also the availability of alternative treatments, and here we have the third massive anomaly.
We’ve seen a clear suppression of information showing that there are not just one but several effective remedies that could reduce the risk of COVID-19 to a number of cohorts down to virtually zero. Examples include hydroxychloroquine and ivermectin, both of which have been safely used for decades in many millions of people around the world.
The precautionary principle dictates that as long as a drug or treatment strategy doesn’t do harm, even if the positive effect may be small, it should be used until better data or better treatments becomes available. This is the logic they used with masks (even though the data overwhelmingly showed no statistical benefit and there are a number of potential harms).
But when it comes to hydroxychloroquine and ivermectin, they suppressed the use of these drugs even though they are extremely safe when used in the appropriate doses and have been shown to work really well in many dozens of studies. As noted by Kirsch in his article:15
“Repurposed drugs [such as hydroxychloroquine and ivermectin] are safer and more effective than the current vaccines. In general, early treatment with an effective protocol reduces your risk of dying by more than 100X so instead of 600,000 deaths, we’d have fewer than 6,000 deaths. NOTE: The vaccine has already killed over 6,000 people and that’s from the vaccine alone (and doesn’t count any breakthrough deaths).”
Doctors are also being muzzled and their warnings suppressed and censored. Dr. Charles Hoffe has administered Moderna’s COVID-19 “vaccine” to 900 of his patients. Three are now permanently disabled and one has died. After writing an open letter to Dr. Bonnie Henry, the provincial health officer for British Columbia, in which he stated that he’s “been quite alarmed at the high rate of serious side-effects from this novel treatment,”16 his hospital privileges were yanked.
Bioethics Laws Are Clearly Being Broken
In a May 30, 2021, essay,17 Malone reviewed the importance of informed consent, rightly concluding that censorship makes it so that informed consent simply cannot be given. Informed consent isn’t just a nice idea or an ideal. It is the law, both nationally and internationally. The current vaccine push also violates bioethical principles in general.
“By way of background, please understand that I am a vaccine specialist and advocate, as well as the original inventor of the mRNA vaccine (and DNA vaccine) core platform technology. But I also have extensive training in bioethics from the University of Maryland, Walter Reed Army Institute of Research, and Harvard Medical School, and advanced clinical development and regulatory affairs are core competencies for me,” Malone writes.
“Why is it necessary to suppress discussion and full disclosure of information concerning mRNA reactogenicity and safety risks? Let’s analyze the vaccine-related adverse event data rigorously. Is there information or patterns that can be found, such as the recent finding of the cardiomyopathy signals, or the latent virus reactivation signals?
We should be enlisting the best biostatistics and machine learning experts to examine these data, and the results should — no must — be made available to the public promptly. Please follow along and take a moment to examine the underlying bioethics of this situation with me …
The suppression of information, discussion, and outright censorship concerning these current COVID vaccines which are based on gene therapy technologies cast a bad light on the entire vaccine enterprise. It is my opinion that the adult public can handle information and open discussion. Furthermore, we must fully disclose any and all risks associated with these experimental research products.
In this context, the adult public are basically research subjects that are not being required to sign informed consent due to EUA waiver. But that does not mean that they do not deserve the full disclosure of risks that one would normally require in an informed consent document for a clinical trial.
And now some national authorities are calling on the deployment of EUA vaccines to adolescents and the young, which by definition are not able to directly provide informed consent to participate in clinical research — written or otherwise.
The key point here is that what is being done by suppressing open disclosure and debate concerning the profile of adverse events associated with these vaccines violates fundamental bioethical principles for clinical research. This goes back to the Geneva convention and the Helsinki declaration.18 There must be informed consent for experimentation on human subjects.”
Experimentation without proper informed consent also violates the Nuremberg Code,19 which spells out a set of research ethics principles for human experimentation. This set of principles were developed to ensure the medical horrors discovered during the Nuremberg trials at the end of World War II would never take place again.
Lines Have Been Crossed That Must Never Be Crossed
In the U.S., we also have the Belmont report,20 cited in Malone’s essay, which spells out the ethical principles and guidelines for the protection of human subjects of research, covered under the U.S. Code of Federal Regulations 45 CFR 46 (subpart A). The Belmont report describes informed consent as follows:
“Respect for persons requires that subjects, to the degree that they are capable, be given the opportunity to choose what shall or shall not happen to them. This opportunity is provided when adequate standards for informed consent are satisfied.
While the importance of informed consent is unquestioned, controversy prevails over the nature and possibility of an informed consent. Nonetheless, there is widespread agreement that the consent process can be analyzed as containing three elements: information, comprehension and voluntariness.”
Americans, indeed the people of the whole earth, are being prevented from freely accessing and sharing information about these gene therapies. Worse, we are misled by fact checkers and Big Tech platforms that ban or put misinformation labels on anyone and anything discussing them in a critical or questioning way. The same censorship also prevents comprehension of risk.
Lastly, government and any number of vaccine stakeholders are encouraging companies and schools to make these experimental injections mandatory, which violates the rule of voluntariness. Government and private businesses are also creating massive incentives to participate in this experiment, including million-dollar lotteries and full college scholarships. None of this is ethical or even legal. As noted by Malone:21
“… as these vaccines are not yet market authorized (licensed), coercion of human subjects to participate in medical experimentation is specifically forbidden. Therefore, public health policies which meet generally accepted criteria for coercion to participate in clinical research are forbidden.
For example, if I were to propose a clinical trial involving children and entice participation by giving out ice cream to those willing to participate, any institutional human subjects safety board (IRB) in the United States would reject that protocol.
If I were to propose a clinical research protocol wherein the population of a geographic region would lose personal liberties unless 70% of the population participated in my study, once again, that protocol would be rejected by any US IRB based on coercion of subject participation. No coercion to participate in the study is allowed.
In human subject clinical research, in most countries of the world this is considered a bright line that cannot be crossed. So, now we are told to waive that requirement without even so much as open public discussion being allowed? In conclusion, I hope that you will join me; stop to take a moment and consider for yourself what is going on. The logic seems clear to me.
1)An unlicensed medical product deployed under emergency use authorization (EUA) remains an experimental product under clinical research development.
2)EUA authorized by national authorities basically grants a short-term right to administer the research product to human subjects without written informed consent.
3)The Geneva Convention, the Helsinki declaration, and the entire structure which supports ethical human subjects research requires that research subjects be fully informed of risks and must consent to participation without coercion.”
Again, if your schedule allows, I sincerely hope you take the time to listen to Weinstein’s interview with Malone and Kirsch. Yes, it is very long — about 3 ½ hours — but they are all astute in their observations, which makes for an enlightening conversation. And remember to read and widely share Kirsch’s article, “Should You Get Vaccinated?”22
- 1, 17, 21 Trial Site News May 30, 2021
- 2, 6, 7, 15, 22 Trial Site News May 25, 2021
- 3 Newzworldtoday.com June 2, 2021
- 4 Trial Site News June 6, 2021
- 5 Letter to Editor, Comment on mRNA COVID-19 Vaccine Safety in Pregnant Persons (PDF)
- 8 Ottawa Citizen June 4, 2021
- 9 The Defender June 15, 2021
- 10 Science May 14, 2021; 372(6543): 738-741
- 11 Archives of Disease in Childhood 2020;105:618-619
- 12 Annals of Internal Medicine September 2, 2020 DOI: 10.7326/M20-5352
- 13 medRxiv June 5, 2021 DOI: 10.1101/2021.06.01.21258176
- 14 News Medical Life Sciences June 8, 2021
- 16 Open Letter from Dr. Charles Hoffe April 5, 2021
- 18 World Medical Association WMA Declaration of Helsinki
- 19 Nuremberg Code of 1947
- 20 HHS.gov The Belmont Report
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Big Pharma’s Five Major Minions that Everyone, Vaxxed or Unvaxxed, Must Oppose
This is not an “anti-vaxxer” article, per se. It’s a call for everyone to wake up to the nefarious motives behind vaccine mandates, booster shots, and condemnation of freedom.
The worst kept secret in world history SHOULD be that the unquenchable push for universal vaccinations against Covid-19 has little if anything to do with healthcare and everything to do with Big Pharma’s influence over the narrative. Unfortunately, that secret has stayed firmly hidden from the vast majority of people because of the five major minions working on behalf of Big Pharma.
What’s even worse is the fact that Big Pharma’s greed is merely a smokescreen to hide an even darker secret. We’ll tackle that later. First, let’s look at the public-facing ringleaders behind the vaccine push, namely Big Pharma. But before we get into their five major minions, it’s important to understand one thing. This is NOT just an article that speaks to the unvaccinated. Even those who believe in the safety and effectiveness of the vaccines must be made aware of agenda that’s at play.
Let’s start with some facts. The unvaccinated do NOT spread Covid-19 more rampantly than the vaccinated. Even Anthony Fauci acknowledged the viral load present in vaccinated people is just as high as in the unvaccinated. This fact alone should demolish the vaccine mandates as it demonstrates they have absolutely no effect on the spread of the disease. But wait! There’s definitely more.
This unhinged push to vaccinate everyone defies science. Those with natural immunity may actually have their stronger defenses against Covid-19 hampered by the introduction of the injections which fool the body into creating less-effective antibodies. Moreover, the push to vaccinate young people is completely bonkers. The recovery rate for those under the age of 20 is astronomical. Children neither contract, spread, nor succumb to Covid-19 in a statistically meaningful way. What they DO succumb to more often than Covid-19 are the adverse reactions to the vaccines, particularly boys.
All of this is known and accepted by the medical community, yet most Americans are still following the vaccinate-everybody script. It requires pure cognitive dissonance and an overabundant need for confirmation bias to make doctors and scientists willingly go along with the program. Yet, here we are and that should tell you something.
Before I get to the five major minions of of Big Pharma, I must make the plea for help. Between cancel culture, lockdowns, and diminishing ad revenue, we need financial assistance in order to continue to spread the truth. We ask all who have the means, please donate through our GivingFuel page or via PayPal. Your generosity is what keeps these sites running and allows us to expand our reach so the truth can get to the masses. We’ve had great success in growing but we know we can do more with your assistance.
Who does Big Pharma control? It starts with the obvious people, the ones who most Americans believe are actually behind this push. Our governments at all levels as well as governments around the world are not working with Big Pharma. They are working for Big Pharma. Some are proactive as direct recipients of cash. Others may oppose Big Pharma in spirit but would never speak out because they know anyone who does has no future in DC.
This may come as a shock to some, but it’s Big Pharma that drives the narrative and sets the agenda for the “experts” at the CDC, FDA, WHO, NIH, NIAID, and even non-medical government organizations.
Most believe it’s the other way around. They think that Big Pharma is beholden to the FDA for approval, but that’s not exactly the case. They need approval for a majority of their projects, but when it comes to the important ones such as the Covid injections, Big Pharma is calling the shots. They have the right people in the right places to push their machinations forward.
That’s not to say that everyone at the FDA is in on it. Big Pharma only needs a handful of friendlies planted in leadership in order to have their big wishes met. We have seen people quitting the FDA in recent weeks for this very reason. The same can be said about the other three- and five-letter agencies. Too many people in leadership have been bribed, bullied, or blackmailed into becoming occasional shills for the various Big Pharma corporations. Some have even been directly planted by Big Pharma. That’s the politics of healthcare and science that drives such things as Covid-19 “vaccines.”
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JD Rucker – EIC