Showing posts with label NIH. Show all posts
Showing posts with label NIH. Show all posts

Make America Healthy Again: How Pharmaceutical Industry Distrust Has Awakened a Sleeping Giant


In recent years, a growing distrust of the pharmaceutical industry has ignited a powerful movement towards personal health, wellness, and alternative care. Americans are increasingly turning away from pharmaceutical solutions and opting for preventive measures, natural remedies, and lifestyle changes to maintain their health. This shift in mindset reflects a cultural awakening, where individuals are reclaiming control of their well-being and demanding more transparency, accountability, and access to natural health alternatives. But how did we get here?

The Growing Distrust in the Pharmaceutical Industry

Why is Harvard Trying to Rebrand The Narrative from "Long Covid" to "Post Infectious"?

Nanoscientist & Harvard Professor Charles Lieber Charged Federally For Ties To China

Long Covid Action Project - End A Disease That Was Created In A Lab

Long Covid Action Project - End The Disease That Was Created In A Lab

China’s former top COVID official admits he can’t rule out lab leak theory

The Chinese official who played a leading role in Beijing's response to COVID-19 has acknowledged the possibility of a lab leak as the source of the deadly virus. 

List of COVID Disinformation Spreaders That Need To Be Investigated

US Surgeon General Vivek Murthy

Steve Kirsch believe that all of these people are involved in “The proliferation of false or misleading narratives, which sow discord or undermine public trust in U.S. government institutions” and have collectively led to the tragic death of over 1M Americans.

What Is The Big Pharma "Con Job" Theory

When NIAID was refused patents for mRNA "Vaccines"! What Did They Do?

How to Create a Pandemic. The Next Big Idea.

Con Job Definitionnoun informal. an act or instance of duping or swindling. an act or instance of lying or talking glibly to convince others or get one's way.

When Dr. Kory testified before the U.S. Senate on December 8, 2020, the message was clear: Ivermectin might well be able to bring the COVID-19 virus to a spectacular halt. Studies were cited that should have convinced experts and laymen alike. Dr. Kory's testimony appeared on YouTube, but—no surprise—it was soon removed by the platform for being "dangerous and misleading". So why did the pharmaceutical industry, the NIH, CDC, NIAID and FDA ignore Dr. Kory?

Everyone knows why, or at least the obvious reason why: a cheap, safe and effective treatment would torpedo Big Pharma's plans to make $$$illions from their rushed-to-market experimental mRNA treatments. The problem, not buried in the fine print, but nonetheless not widely trumpeted at the time: An Emergency Use Authorization for a medical product, such as the EUA sought by Big Pharma for mRNA gene therapy, cannot be granted if there exists a viable and safe treatment for the disease that the experimental product has targeted:

"FDA may authorize unapproved medical products or unapproved uses of approved medical products...when certain criteria are met, including there are no adequate, approved, and available alternatives."

There it is: Ivermectin accepted as a treatment, no EUA for mRNA, no Big Bucks for Big Pharma. As a truly humanitarian gesture, the Senate Committee could have insisted, or at least recommended that an EUA be immediately issued for Ivermectin, but nooooo. A behind-the-scenes eight-hundred-pound gorilla effect?

If one refers back to a 2004 article in the New York Review of Books by Marcia Angell, formerly editor of the prestigious New England Journal of Medicine, (New York Review of Books JULY 15, 2004 ISSUE) we clearly see a few key facts about Big Pharma that provide important background for understanding the present Big Pharma Phiasco. (Bold type emphasis added in the following excerpt.)

"Over the past two decades the pharmaceutical industry has moved very far from its original high purpose of discovering and producing useful new drugs. Now primarily a marketing machine to sell drugs of dubious benefit, this industry uses its wealth and power to co-opt every institution that might stand in its way, including the US Congress, the FDA, academic medical centers, and the medical profession itself.

"What does the eight-hundred-pound gorilla do? Anything it wants to.

"What’s true of the eight-hundred-pound gorilla is true of the colossus that is the pharmaceutical industry. It is used to doing pretty much what it wants to do. The watershed year was 1980. Before then, it was a good business, but afterward, it was a stupendous one. From 1960 to 1980, prescription drug sales were fairly static as a percent of US gross domestic product, but from 1980 to 2000, they tripled. They now stand at more than $200 billion a year. Of the many events that contributed to the industry’s great and good fortune, none had to do with the quality of the drugs the companies were selling.

"As their profits skyrocketed during the 1980s and 1990s, so did the political power of drug companies. By 1990, the industry had assumed its present contours as a business with unprecedented control over its own fortunes. For example, if it didn’t like something about the FDA, the federal agency that is supposed to regulate the industry, it could change it through direct pressure or through its friends in Congress.

"When I say this is a profitable industry, I mean really profitable. It is difficult to conceive of how awash in money big pharma is. Drug industry expenditures for research and development, while large, were consistently far less than profits. For the top ten companies, they amounted to only 11 percent of sales in 1990, rising slightly to 14 percent in 2000. The biggest single item in the budget is neither R&D nor even profits but something usually called “marketing and administration”—a name that varies slightly from company to company. In 1990, a staggering 36 percent of sales revenues went into this category, and that proportion remained about the same for over a decade. Note that this is two and a half times the expenditures for R&D.

"[But] the industry [now] faces ... problems. It happens that, by chance, some of the top- selling drugs—with combined sales of around $35 billion a year—are scheduled to go off patent within a few years of one another. This drop over the cliff began in 2001, with the expiration of Eli Lilly’s patent on its blockbuster antidepressant Prozac. In the same year, AstraZeneca lost its patent on Prilosec, the original “purple pill” for heartburn, which at its peak brought in a stunning $6 billion a year. Bristol-Myers Squibb lost its best-selling diabetes drug, Glucophage. The unusual cluster of expirations will continue for another couple of years. While it represents a huge loss to the industry as a whole, for some companies it’s a disaster. Schering-Plough’s blockbuster allergy drug, Claritin, brought in fully a third of that company’s revenues before its patent expired in 2002. Claritin is now sold over the counter for much less than its prescription price. So far, the company has been unable to make up for the loss by trying to switch Claritin users to Clarinex—a drug that is virtually identical but has the advantage of still being on patent.

"Even worse is the fact that there are very few drugs in the pipeline ready to take the place of blockbusters going off patent. In fact, that is the biggest problem facing the industry today, and its darkest secret. All the public relations about innovation is meant to obscure precisely this fact. The stream of new drugs has slowed to a trickle, and few of them are innovative in any sense of that word. Instead, the great majority are variations of oldies but goodies—“me- too” drugs.

"Of the seventy-eight drugs approved by the FDA in 2002, only seventeen contained new active ingredients, and only seven of these were classified by the FDA as improvements over older drugs. The other seventy-one drugs approved that year were variations of old drugs or deemed no better than drugs already on the market. In other words, they were me-too drugs. Seven of seventy-eight is not much of a yield. Furthermore, of those seven, not one came from a major US drug company.

"For the first time, in just a few short years, the gigantic pharmaceutical industry is finding itself in serious difficulty. It is facing, as one industry spokesman put it, “a perfect storm.” To be sure, profits are still beyond anything most other industries could hope for, but they have recently fallen, and for some companies they fell a lot. And that is what matters to investors...

"...Nevertheless, the industry keeps promising a bright new day. It bases its reassurances on the notion that the mapping of the human genome and the accompanying burst in genetic research will yield a cornucopia of important new drugs.

"The industry is also being hit with a tidal wave of government investigations and civil and criminal lawsuits. The litany of charges includes illegally overcharging Medicaid and Medicare, paying kickbacks to doctors, engaging in anticompetitive practices, colluding with generic companies to keep generic drugs off the market, illegally promoting drugs for unapproved uses, engaging in misleading direct-to-consumer advertising, and, of course, covering up evidence. Some of the settlements have been huge. TAP Pharmaceuticals, for instance, paid $875 million to settle civil and criminal charges of Medicaid and Medicare fraud in the marketing of its prostate cancer drug, Lupron. All of these efforts could be summed up as increasingly desperate marketing and patent games, activities that always skirted the edge of legality but now are sometimes well on the other side.

"How is the pharmaceutical industry responding to its difficulties? One could hope drug companies would decide to make some changes—trim their prices, or at least make them more equitable, and put more of their money into trying to discover genuinely innovative drugs, instead of just talking about it. But that is not what is happening. Instead, drug companies are doing more of what got them into this situation. They are marketing their me-too drugs even more relentlessly. They are pushing even harder to extend their monopolies on top-selling drugs. And they are pouring more money into lobbying and political campaigns. As for innovation, they are still waiting for Godot.

"This is an industry that in some ways is like the Wizard of Oz—still full of bluster but now being exposed as something far different from its image. Instead of being an engine of innovation, it is a vast marketing machine. Instead of being a free market success story, it lives off government-funded research and monopoly rights. Yet this industry occupies an essential role in the American health care system, and it performs a valuable function, if not in discovering important new drugs at least in developing them and bringing them to market. But big pharma is extravagantly rewarded for its relatively modest functions. We get nowhere near our money’s worth.

"Clearly, the pharmaceutical industry is due for fundamental reform. Reform will have to extend beyond the industry to the agencies and institutions it has co-opted, including the FDA and the medical profession and its teaching centers." [end of excerpt, posted without permission under the "Fair Use" rulings regarding the 1976 Copyright Act for NON-profit academic, research, and general information purposes.]

And clearly, the evidence so diligently exposed by Marcia Angell demonstrates that the pharmaceutical industry—even by the turn of the century—had itself become a systemic chronic disease typical of the capitalist extreme, needing a cure that the patient resists at every turn for there is only one way to cure such a disease. "Reform"? It is a lesson as old as capitalism itself: when an industry grows and grows beyond all reasonable bounds, acquires the means to control its future through big money, bribes, kickbacks, dirty tricks, cheating, murder, crimes against humanity ...and then unforseen circumstances begin to erode the cash-flow.... I need hardly say what the cure is.

All that exposed in 2004! What, then, is the situation today?

Let's go back to the original topic here: already in the early years of the century the pharmaceutical industry was in trouble, looking for "new ways" to keep the big bucks flowing. And now we see Dr. David Martin's patent research evidence, showing that Big Pharma was patenting everything they could dream up, why not? They all surely have big teams of patent lawyers et al., and who knows, if they came to own every conceivable new idea from medical—especially genetic—research, it might all fall into place. "It"?

Patents for mRNA technology, COVID viruses and modifications such as "gain-of-function"—as revealed by Dr. David Martin—were amassed by Big Pharma through the Noughties and Teenies, including patents on the spike protein itself, and eventually arrived to the attempt to patent a general-purpose accepted-by-all remedy for avoiding seasonal flu if not the entire range of such possible viruses. As Marcia Angell notes, vaccines, whether they be classic ones, or the new mRNA techolgy-based injections (technically they are not "vaccines"), remain one of the biggest money-makers for Big Pharma. So we can deduce the mRNA technique was supposed to finally save the industry and restore growth and profitability.

But, disaster!, Tony Fauci and National Institute of Allergy and Infectious Diseases (NIAID) were refused patents for mRNA "vaccines"! Oh dear me! What to do?  

Read the Fauci Dossier

Tony and his Big Pharma pals were enraged they couldn’t get a patent on an all-purpose-general-use-mRNA-flu-shot, to be accepted by all good little boys and girls the world over so they wouldn't get the sniffles for Christmas and give a possibly fatal dose to grandma. A "remedy" not only for the sniffles and grandma but for big pharma too—the key to continue to maintain/expand their profits with a new, (patented) revolutionary miracle technique. So the light-bulb pops above Tony’s head as in a Beavis & Butthead classic, “Hey Beavis! Those fart-knockers won't give us a patent? Let’s INTRODUCE the disease we need to get such a vaccine launched. Yeah! he-he-he, huh-huh-huh. Cool!"

My reference here might be thought crude and insulting, but while there are surely many very clever people involved in the Big Pharma Phiasco, scientists, directors, politicians, et al., there appear to be few, if any, who might be thought of as wise. Under the circumstances, the clever be damned.

Now, it seems settled that the research that led to COVID-19 was bioweapon-oriented. But that does not prove it was released (also a near-certainty) intentionally as a bioweapon. That may have happened a little later, as a side-line of the big-money project when Big Pharma chatted with the Pentagon, and it was thought a cool idea to infect some Iranian leaders. Primarily, COVID was released so that Fauci, NIAID & Big Pharma could then demand an EUA and get eventual patents on all such mRNA treatments. But for COVID these people had research indicating they knew the spike protein that was generated by the injection did not remain localized but spread to many organs in the body. What if that should cause "spike protein disease"? It was probably thought that the problem would be minor, and if enough pressure and propaganda be applied, success in "vaccinating the world" could still be achieved, and collateral damage ignored. Unfortunately the spike protein complication resulted in a great many deaths and serious injuries, far, far outnumbering such negative outcomes which in previous incidences of introduction of vaccines, were sufficient to immediately force a withdrawal of the product from further testing.

But the push for world vaccination continues, with such force that one begins, or rather continues to wonder why. Some see a conspiracy to reduce world population. I'd need at least some extensive whistleblower hard data before I'd credit the long list of perpetrators as being that competent, to have planned this thing from the get-go. So far I have to see the whole thing as a Colossal Con Job for Big Bucks turned into a Colossal SNAFU for which the perps are trying very hard to cover their dorsal protuberances. The whole affair is typical of very clever but very unwise participants. Indeed, as a sequel to The Sting, it has been a rip-roaring success, one that you should be embarrassed for having fallen for. As a plan to reduce population, that's strictly sci-fi. If that's the case, the SNAFU is even bigger since the populations dying off most successfully seem to be we Westerners. But Indians, Mexicans, S. Americans... citizens of nations and regions taking the Ivermectin/HCQ route? Apparently they would be the preponderant survivors.

So now that everyone knows we have been mightily deceived, wouldn't there be some better course of action for Big Pharma, the NIH, CDC, NIAID and FDA that could admit error, preserve profit, avoid criminal charges, avoid all sorts of horrible (for Big Pharma) outcomes, and actually benefit society by combining everything we surely now know....

Well, since there is not the least hint from them that they know we know they have been caught out, perhaps we are in store for the next big thing—oh so clever!—whether dreamed up well in advance, or perhaps just recently appearing on the drawing boards: the next medical product that will seal the fate of humanity in partnership with an ever-expanding BIG PHARMA presence and profits-spree. If spike protein has caused problems, why not introduce (after a maximum have been mRNA'd of course) a spike protein cleaner-upper, a scavenger of spike protein residues in the body that will solve all the residual post-vaccination and post-COVID-19 disease problems. Come one, come all! One dose of this miracle oil will Hoover up all harmful COVID residues! Take a third mortgage on your house if necessary! Is such a drug possible? If so, you can bet your bottom dollar on it being even more expensive than Remdesivir, and available only for the privileged, the heavily insured, and third mortgagees.

As Yogi Berra once quipped, "Predictions are hard to make, especially about the future". However, I would certainly be surprised if the Big Pharma Phiasco is not destined for several more entertaining chapters. Be ready. Don't participate ! Stay well !!

Military Documents About Gain of Function Contradict Fauci Testimony Under Oath

Ecohealth Darpa

Military Documents About Gain of Function Contradict Fauci Testimony Under Oath. 

Military documents state that EcoHealth Alliance approached DARPA in March 2018 seeking funding to conduct gain of function research of bat borne coronaviruses. The proposal, named Project Defuse, was rejected by DARPA over safety concerns and the notion that it violates the gain of function research moratorium.

REJECTION OF DEFUSE PROJECT PROPOSAL

EXECUTIVE SUMMARY: DEFUSE

BROAD AGENCY ANNOUNCEMENT PREventing EMerging Pathogenic Threats(PREEMPT)

U.S. Marine Corp Major Joseph Murphy's Report to Inspector General of DoD

The main report regarding the EcoHealth Alliance proposal leaked on the internet a couple of months ago, it has remained unverified until now. Project Veritas has obtained a separate report to the Inspector General of the Department of Defense, written by U.S. Marine Corp Major, Joseph Murphy, a former DARPA Fellow.

“The proposal does not mention or assess potential risks of Gain of Function (GoF) research,” a direct quote from the DARPA rejection letter.

Project Veritas has obtained startling never-before-seen documents regarding the origins of COVID-19, gain of function research, vaccines, potential treatments which have been suppressed, and the government’s effort to conceal all of this.

The documents in question stem from a report at the Defense Advanced Research Projects Agency, better known as DARPA, which were hidden in a top secret shared drive.

DARPA is an agency under the U.S. Department of Defense in charge of facilitating research in technology with potential military applications.

Project Veritas has obtained a separate report to the Inspector General of the Department of Defense written by U.S. Marine Corp Major, Joseph Murphy, a former DARPA Fellow.

The report states that EcoHealth Alliance approached DARPA in March 2018, seeking funding to conduct gain of function research of bat borne coronaviruses. The proposal, named Project Defuse, was rejected by DARPA over safety concerns and the notion that it violates the basis gain of function research moratorium.

According to the documents, NIAID, under the direction of Dr. Fauci, went ahead with the research in Wuhan, China and at several sites across the U.S.

Dr. Fauci has repeatedly maintained, under oath, that the NIH and NAIAD have not been involved in gain of function research with the EcoHealth Alliance program. But according to the documents obtained by Project Veritas which outline why EcoHealth Alliance’s proposal was rejected, DARPA certainly classified the research as gain of function. 

“The proposal does not mention or assess potential risks of Gain of Function (GoF) research,” a direct quote from the DARPA rejection letter.

Major Murphy’s report goes on to detail great concern over the COVID-19 gain of function program, the concealment of documents, the suppression of potential curatives, like Ivermectin and Hydroxychloroquine, and the mRNA vaccines.

Project Veritas reached out to DARPA for comment regarding the hidden documents and spoke with the Chief of Communications, Jared Adams, who said, “It doesn’t sound normal to me,” when asked about the way the documents were shrouded in secrecy. “If something resides in a classified setting, then it should be appropriately marked,” Adams said. “I’m not at all familiar with unmarked documents that reside in a classified space, no.”

In a video breaking this story published on Monday night, Project Veritas CEO, James O’Keefe, asked a foundational question to DARPA:

“Who at DARPA made the decision to bury the original report? They could have raised red flags to the Pentagon, the White House, or Congress, which may have prevented this entire pandemic that has led to the deaths of 5.4 million people worldwide and caused much pain and suffering to many millions more.”

Dr. Anthony Fauci has not yet responded to a request for comment on this story.

Senior NIH Matthew Memoli Pushes Back on Vaccine Mandates

Matthew Memoli favors vaccinations in vulnerable populations but argues population-level vaccination could hinder the development of a natural, robust immunity gained through infection.

Story at a glance

An unvaccinated doctor who heads a research team at the National Institutes of Allergy and Infectious Disease is leading a debate within the National Institute of Health over the ethics of COVID-19 vaccine mandates.

Matthew Memoli reportedly wrote in an email to NAID Director Anthony Fauci in July that he found mandated vaccinations “extraordinarily problematic.”

“I think the way we are using the vaccines is wrong,” he told Fauci.

An unvaccinated doctor who heads a research team at the National Institutes of Allergy and Infectious Disease (NIAID) is leading a debate within the National Institute of Health (NIH) over the ethics of COVID-19 vaccine mandates. 

Matthew Memoli, a 16-year veteran at the NIH, will argue against vaccine mandates in a Dec. 1 live-streamed roundtable session over the ethics of mandates, which will be open for viewing within the agency, to patients and to the public, The Wall Street Journal reported. 

“There’s a lot of debate within the NIH about whether [a vaccine mandate] is appropriate,” David Wendler, a senior NIH bioethicist in charge of planning the session, told WSJ. “It’s an important, hot topic.”

An appeals court on Saturday temporarily stopped President Biden’s mandate requiring employers to verify employee vaccination or ensure weekly testing. 

Memoli reportedly wrote in an email to NIAID Director Anthony Fauci in July that he found mandated vaccinations “extraordinarily problematic.” 

“I think the way we are using the vaccines is wrong,” he told Fauci. 

Our country is in a historic fight against the coronavirus. Add Changing America to your Facebook or Twitter feed to stay on top of the news.

Memoli, who has reportedly applied for vaccine exemptions, favors vaccinations in vulnerable populations but argues population level vaccination could hinder the development of a natural, robust immunity gained through infection. 

The 48-year-old has said his children have received their childhood vaccinations, and he will support the results of the ethics discussion regardless of the outcome. 

“I do vaccine trials. I, in fact, help create vaccines,” he told WSJ. “Part of my career is to share my expert opinions, right or wrong.…I mean, if they all end up saying I’m wrong, that’s fine. I want to have the discussion.”

The Centers for Disease Control and Prevention (CDC) published new findings last month that suggest vaccines are the most effective protection against the virus. 

The data in the study “demonstrate that vaccination can provide a higher, more robust, and more consistent level of immunity to protect people from hospitalization for COVID-19 than infection alone for at least 6 months.”

NIH Deleted "Gain-Of-Function Research" on Website After Whistleblower

gain-of-function research epp research


Fauci ignores responsibility wants to argue semantics. The dude is insane. The arrogance of career people like Fauci is chilling. How is he not being trialed for crimes against humanity?

For those that don’t know - this is how they defined “gain-of-function” on their website until at least October 19th, 2021. It looks like this section was deleted, and the page was edited, immediately after the NIH whistleblower came out "NIH confirmed that EcoHealth violated the terms of their grant".  

15 things everyone needs to know about COVID and how to treat it

Steve Kirsch treatment tips
  1. Avoid all the COVID vaccines, even Novavax. Just say no. It’s not for anyone. No exceptions. The data show that these vaccines kill more people than they save. You can end up dead or disabled or with a compromised immune system for the rest of your life. For kids, for example, we will kill over 100 kids to save 1 life from COVID. These are the most dangerous vaccines ever deployed; 800x more deadly than the smallpox vaccine. Novavax has a much better safety profile than the current vaccines, but there may be serious, longer term risks here that we need to quantify. It’s not their fault… the spike protein is particularly toxic because it was designed to be toxic (I’m friends with Li-Meng Yan; we talk). The experts I work with say “not enough data.” So our advice is let’s wait for the data and use early treatment in the meantime. You can never unvaccinate yourself and right now early treatments are a great solution with higher efficacy and known safety.
  2. If you get COVID, start early treatment ASAP as soon as you have symptoms. Early treatment is much safer and there is a much lower chance of long haul COVID, MIS-C, and adverse events. See my treatment advice for details; many options are available without a doctor or prescription. The immunity you acquire from getting the real virus is both robust and durable.
  3. Make sure you have your early treatment drugs already in your house so you can start treatment as soon as you have symptoms.
  4. If you aren’t sure you have COVID, you can get a PCR test, but these can be inaccurate. If you have symptoms, you can use a home test kit such as the binax now kit (Note: they will not work unless you currently are symptomatic, so don’t use these kits for employer screening; it’s a complete waste of money).
  5. The mainstream media wants to keep you in the dark about the truth about these vaccines so they only tell you one side of the story and they censor competent speakers on the other side. This is why you will never see Peter McCullough on CNN, in the NY Times, etc. They will never sponsor a debate between the top experts on both sides because that would destroy the false narrative and damage the reputation of the mainstream media. So they have to tell only one side of the narrative.
  6. The whole pandemic response was unnecessary. The lockdowns, social distancing, masking, business restrictions, etc. We knew back in March 2020 that a cocktail of repurposed drugs given early could keep people out of the hospital and turn COVID into a mild cold with no long-term side effects.
  7. The NIH is deliberately suppressing early treatments that work like fluvoxamine, ivermectin, vitamin D, inhaled budesonide, etc. Even after fluvoxamine was proven in a large Phase 3 clinical trial with an incredible 12X reduction in hospitalization, the NIH did nothing. Absolutely nothing. They do not want you to know about fluvoxamine. When Fareed and Tyson tried to get the NIH and FDA’s attention in March 2020 on their protocol which has a 99.76% risk reduction (better than anything else), they were ignored.
  8. Masks don’t work. It is political theater to prove they can use fear to get you to do nonsensical things. Nobody will debate my team on this because it would destroy their argument.
  9. Never trust the CDC, FDA, NIH, and medical community again. This is the most dangerous vaccine in human history and the CDC couldn’t find a single safety signal (it was the DoD that spotted myocarditis). The NIH is sand-bagging early treatment. The mainstream medical community is basically believing everything the FDA and CDC are telling them without bothering to double-check anything.
  10. Avoid the hospital. If you do get hospitalized, refuse intubation and remdesivir. Get a court order to get cyproheptadine, fluvoxamine, and/or ivermectin. You will need a court order because all hospitals will refuse these proven treatments. See the list of hospitalized treatment protocols.
  11. They could end vaccine hesitancy worldwide anytime they wanted. All they have to do is agree to a single 3 hour debate. But none of the so-called experts who claim the vaccines are safe will debate our team. This is because they know they will lose. So they must ignore and censor us. Their unwillingness to have a fair scientific discussion with experts on both sides tells you everything you need to know about who has the better argument.
  12. If you maintain very high levels of Vitamin D, you can greatly reduce your chance of getting sick from COVID. It’s the simplest thing to do and it is safe and effective. There’s a strong correlation between your vitamin D level and your risk of dying from COVID-19. At a level of 17 ng/mL, the death rate is nearly 100%. At a level of 35 ng/mL, the death rate is near zero. It is inexplicable that the medical community and/or NIH isn’t telling people this.
  13. Fluvoxamine is highly effective if you get COVID. The best dose is 50mg twice a day for 14 days. Take it as soon as you have symptoms. The side effect profile is near zero as long as you avoid coffee. If you can’t get fluvoxamine, you can use 30mg once a day of fluvoxetine. Both drugs work for hospitalized patients as well. Many other drugs are very effective. See my treatment advice for details.
  14. The single best drug if you get COVID is Interferon Lambda, but it is not FDA approved; it is available only in clinical trials. It works because it replaces the interferon that the virus disables when it attacks you. D-dimer is greatly reduced in the treatment group… this is very telling.
  15. The reason all this happened is that people don't double-check authorities. They believe the authorities, and it creates a domino effect. They aren't inherently evil, just trusting the wrong people. They think I'm an evil person because I disagree with the authorities. I disagree because the data doesn’t support what we are being told. Few people (especially doctors) have the time/expertise to understand/analyze VAERS. We haven't found *anyone* in the world who is able to "correct" our calculation. But as long as people think we are misinformation spreaders, nobody listens to us. Most people will make decisions based on the # of “experts” supporting a viewpoint, not by looking at the data directly; few people have the time and expertise to do that. I did that in early May, 2021 and here is the first article I wrote at the time (Should you get vaccinated?) after I was convinced the vaccines were causing harm. I lost a lot of friends after writing that article, but it was the right thing to do and I don’t regret it. I think I’ve made more than 100X new friends by standing up for science and truth. I also found a very odd asymmetry… everyone on our side will happily engage the other side in a discussion on the merit, but not vice versa. They just want to tell us we are wrong, but will not explain to us why we are wrong (since they don’t know).

Rand Paul Grills FRAUDci on Gain-of-Function Research

You've changed the definition of Gain-Of-Function to try to cover your ass 

Rand Paul Grills Fauci

 

Why Is Medical Corruption Being Ignored? 12 Examples

medical corruption

Steve Kirsh's newsletter - I thought I'd start a list to capture what is going on. Nobody in the mainstream medical community seems to mind these abuses. They are remaining silent, so I guess these are all OK nowadays.

  1. Jessica Rose’s paper exposing how dangerous vaccine-induced myocarditis was “temporarily removed” by the publisher of the journal over the objections of the Editor and everyone else. The reason is given: “it wasn’t an invited paper.” That is incorrect since the Editor was the one that handled the paper. It is still removed as of this writing. I don’t think it will ever be re-instated.

  2. Fluvoxamine was shown in a large Phase 3 clinical trial to reduce death from COVID by 12X. This is the most effective drug ever discovered for COVID. Nothing else has a better effect size. All the earlier trials were 100% successful. It even works in hospitalized patients. The FDA, CDC, NIH, and WHO all ignored it. Stunning, but totally expected. It only works if it is from a major US drug company. Repurposed drugs don’t count.

  3. Article in the BMJ shows the corruption of the Pfizer clinical trials depended on by the FDA to justify drug approval. Ignored by the ACIP committee doing the approval on the same day the story hit. They didn’t even mention it. The article noted that even after Pfizer knew about the corruption, they awarded the company four more contracts.

  4. Researchers have to sue the FDA to see the Pfizer data (story and lawsuit). Nobody is revealing the data like they are supposed to do. I wonder why?

  5. Maddie de Garay is paralyzed for life in the Pfizer 12-15 clinical trial. It is reported in the trial results as mild abdominal pain. FDA agrees to investigate but does nothing. No warning is ever given to parents that the vaccine can permanently cripple their child. Nobody seems to mind that the FDA and CDC never investigated it. Mainstream media ignores the story.

  6. One of the world’s top epidemiologists wrote a paper that points out cracks in the false narrative. It easily passes peer review and the publisher tells him it will be published. It is never published.

  7. Fluvoxamine was recommended to be used by doctors on a shared decision-making basis against COVID by a panel of key opinion leaders by more than a 2:1 margin. Written up in Washington Post op-ed. Seven medical journals refuse to publish the meeting notes (after taking months to give an answer). It’s still unpublished. So nobody will know.

  8. The CDC still claims they haven’t found a causal link between death and the COVID vaccines even though autopsy results show definitively that the vaccines are killing people (see this article and this confirmation by other German pathologists).

  9. The CDC still claims that the spike protein is harmless despite numerous peer reviewed papers showing the opposite.

  10. The CDC and NIH ignore ivermectin despite multiple peer-reviewed systematic reviews and meta analyses showing it works. Not only that, they go out of their way to make it hard to get and the AMA recommends people not use it. But this is the highest level of evidence medicine! They aren’t walking the talk for this drug.

  11. Paul Offit and others on the FDA and CDC panel say there are more cases of myocarditis from COVID than from the vaccines. After he’s conclusively shown to be wrong, he doesn’t acknowledge it.

  12. And my personal favorite is that everyone ignores my analysis of the VAERS data showing 150,000 deaths from the vaccine. They told me “it isn’t peer reviewed.” But it is. Lots of my peers have reviewed it and found it very solid. But there are other papers that are peer reviewed and published that show the same result (which I cite at the start). So if I’m wrong about the 150,000 deaths (which I showed 8 different ways), then why won’t anyone show me their “correct” analysis of the data we have? Whenever I ask that question, I get silence. Every time. Nobody in the medical community likes reading stuff that goes against their belief system it seems.

What’s sad is that all of the above corruptions are unambiguous, but leading medical “authorities” are silent on all of them.

I’m sure I missed a lot of things. Please comment below about your favorite example of the corruption of science.

Attorney General Asked If Fauci Will Be Investigated For Lying To Congress


Rep. Andy Biggs (R-AZ) asked Attorney General Merrick Garland during a House Judiciary Committee hearing on Thursday if they would investigate Dr. Fauci for potentially lying to Congress.

NIH States EcoHealth Alliance Violated Terms and Conditions of NIH Grant AI110964

 


This is Fauci throwing Peter Daszak under the bus, in case that is not clear to you.  I predict that this is going to get really ugly now.

- Fauci funded gain-of-function research
- Wuhan lab was doing GOF research
- COVID came out of Wuhan lab
- CCP covered it up 
- Fauci lied to congress

Fauci committed perjury. 

“Dr Death” must face a war crimes tribunal immediately. NIH corrects untruthful assertions by NIH Director Collins and NIAID Director Fauci that NIH had not funded gain-of-function research in Wuhan.

NIH states that EcoHealth Alliance violated Terms and Conditions of NIH grant AI110964.

Healthy mom suffers cascade of health problems after COVID shot, vows to fight medical corruption

5,000+ People in The United States Have Had A Similar ADE Issue According To The NIH.

She is holding a rally and vigil on the steps of the Supreme Court on November 2nd for similar victims. 

A young mother, Brianne Driessen, was eager to sign up for the Astrazeneca COVID shot trial. Almost immediately after getting the injenction, she began experiencing severe adverse reactions, which continue to this day. In this interview with LifeSite’s Jim Hale, Driessen makes a passionate appeal for true informed consent and help for the thousands of fellow victims of the COVID jab.

A young mother from Utah shared with LifeSiteNews her nightmarish experience of developing severe adverse reactions immediately after receiving the COVID jab as part of the AstraZeneca COVID shot trial.

Brianne Dressen from Utah was a healthy mother of two young children and a pre-school teacher who eagerly signed up to the AstraZeneca COVID vaccine trial back in November 2020, as she was “confident that this was going to be our way out of the pandemic.” She received a first dose of the AstraZeneca vaccine on November 4 and started experiencing adverse effects within an hour of getting the shot.

Dressen first experienced tingling in her arm, blurred vision, hyper-sensitivity to sound, light and touch, dizziness, nausea, and leg numbness. Weeks later, she was admitted to the hospital after her legs “stopped working” and she became incontinent. She had to undergo intense physical therapy, including re-learning how to walk.

Dressen was later diagnosed with a number of serious health conditions which affect her nervous system. She shared her ordeal with LifeSiteNews correspondent Jim Hale.

After a first of “many visits to the emergency room” ruled out multiple sclerosis and other major neuro-degenerative disorders, Dressen was sent home where she had to stay in a room by herself because of her extreme sensitivity to sound.

“My sensitivity to sound was so severe that even my little girl’s voice was too much for my ears,” she recalled.

She also suffered from hypersensitivity to light and had to “put towels on the windows to make the room completely black.”

Dressen lost 20 pounds, as she suffered from nausea and vomiting, and experienced difficulties swallowing her food.

She said she was certain that the vaccine was responsible for her condition.

“There is no question in my mind that the vaccine caused this reaction,” she said, before expressing anger and frustration at the fact that AstraZeneca did not investigate her case thoroughly, as would be expected during a clinical trial.

“You would hope that there would be someone who would be appropriately tracking the data, that these cases (even if they’re rare) are evaluated, that they are discussed, that the information is disclosed in a full and transparent manner. Unfortunately, that has not been the case,” she said.

“I really wish I could say that the drug companies did their due diligence with this, but they didn’t,” she added.

Dressen also revealed that her case was not included in the list of severe adverse events that was published by AstraZeneca. “And now there’s their published clinical trial data. I’m not in it,” she said.

AstraZeneca claims to follow up with all serious adverse events cases for up to 720 days but monitored Dressen over a much shorter period of time.

“I definitely was a serious adverse event,” said Dressen, “I was followed up with for 60 days.”

The pharmaceutical giant also agreed in their contract with clinical trial volunteers to pay for any injury or medical need that would result from the vaccine. An agreement that they did not honor in Dressen’s case.

“After months of repeated pleading and fighting with them to help us with the massive pile of medical bills, I have 590 dollars from them.”

For a long time, doctors could not figure out what was wrong with the young mother. They first diagnosed Dressen with “anxiety” from the COVID vaccine. But she was then able to go to the National Institutes of Health (NIH) where she received appropriate diagnoses, which included a number of nervous disorders such as: non-length-dependent neuropathy, short-term memory loss, sensory neuropathy, dysautonomia and severe postural tachycardia syndrome.

The young woman still suffers from these adverse effects to this day, almost a year after having been vaccinated, and her life has not been the same since.

“My body went from functioning at a normal, healthy level; I was able to take care of my kids and my work, too,” she said. “Now, my big accomplishment today will be talking to you and the fact that I made myself breakfast.”

LifeSiteNews correspondent Jim Hale then asked Dressen to discuss how this event changed her views on the pharmaceutical industry.

“This has been very eye opening for me,” replied Dressen, “I feel like I’ve been plucked out of the matrix.”

Dressen explained that she grew increasingly distrustful of government agencies as she witnessed evidence of them purposefully withholding information from the public.

“These [adverse] reactions are not being disclosed to the public,” she said. “Because of this, the public is not being provided informed consent, but also the medical community is not being informed appropriately that these reactions can happen.”

Dressen also claimed that attempts at withholding information on adverse events from the public does not only come from social media platforms but also from within the medical world.

“There’s medical censorship happening,” she said, “there’s censorship with the research; we have researchers that have tried to get case studies published in scientific journals and they can’t get them published.”

The young mother became emotional when she recalled that some of the people suffering from these adverse effects have committed suicide.

“I had to write a eulogy for a dear friend of mine, for her husband to read after she took her life,” she said.

Dressen and Hale then discussed other cases of people that have suffered loss as a result of the vaccine’s adverse effects, including that of Ernest Ramirez, a father from Texas who recently lost his 15-year-old son to the Pfizer vaccine. Hale also mentioned that in a recent interview with LifeSiteNews, Dr. Robert Malone, a pioneer of the mRNA technology used in the development of the COVID vaccines “told us, flat out, if you have an adolescent son, he should not be getting the vaccine.”

Among some of the initiatives taken in response to this issue, Dressen mentioned a website with over 500 testimonies and accounts of people who have suffered from COVID vaccine adverse events.

Additionally, she announced that a press conference is going to take place on November 2 on the steps of the Supreme Court to hold government agencies accountable.

“We’re uniting with those like Ernest Ramirez and we’re going to the capital to plead with our elected officials to help us and to hold these agencies, the FDA, the CDC, the NIH, accountable, because we know acutely just how much they know,” she said.

“They know about the suicides [and] the suicide attempts, they know about people losing their jobs because of inappropriate mandates, they know about the sick kids, they know about people being buried under medical debt and losing their homes, they know about the issues with the clinical trials,” she added.

In conclusion of the interview, Dressen insisted that she was not anti-vaccine and explained that her husband had gotten the COVID vaccine, but she advocated for informed consent and not coercing people.

“I really believe that everybody should have appropriate full informed consent so they can make an appropriate choice for themselves; and also, because there is a risk, there absolutely needs to be a choice,” she said.

She condemned government agencies for letting people who suffer from these adverse events deal with them on their own and for abandoning them.

“The problem is, if you get a vaccine reaction like this, you are completely on your own. The government agencies are not going to help you,” she said. “You will not be able to get financially compensated and your medical teams will have no idea what to do with you.”


Brianne Driessen

COVID Origins Investigator Wins $1 Million Chinese Prize For Claiming Virus Developed Naturally

Dr. Malik Peiris, who previously served on the Lancet medical journal’s COVID-19 origins investigation committee, received China’s “Nobel Prize” for research affirming the Chinese Communist Party’s false narrative that COVID-19 developed naturally.

Peiris, a Sri Lankan virologist working in Hong Kong, was one of 12 scientists leading the now-defunct Lancet probe into the origins of COVID-19. While the task force is no longer listed on the medical journal’s website, as it was forced to disband due to extensive conflicts of interests with the Wuhan Institute of Virology, archived web pages reveal Peiris’s participation in the effort.

Following Peiris’s stint on the task force, the Chinese Communist Party awarded him with the prize in life sciences in the 2021 Future Science Prize – dubbed China’s “Nobel Prize.” China’s top scientific honor is accompanied by a $1 million prize, which is funded by several Chinese Communist Party-linked companies such as Baidu, Hillhouse Capital, and Sequoia Capital China.

State-run media outlet Global Times claimed the award was for his “major discoveries of SARS-CoV-1 as the causative agent of the global SARS outbreak in 2003 with impact on combating COVID-19 and emerging infectious diseases.” Peiris shared the award with co-author Kwok-Yung Yuen.

In an exclusive interview with the Chinese Communist Party-run media outlet, Yuen asserted “this is one of the most important prizes not just in China but also internationally.”

Peiris’s research was praised by award reviewers as playing an integral role in tracing the origins of COVID-19, as reviewer Wang Xiaodong noted “Chinese scientists were able to quickly identify the cause of the COVID-19 pandemic thanks to their contributions.” The research bolstered the Chinese Communist Party’s fake narrative that COVID-19 developed naturally as opposed to escaping from a lab.

As Global Times explains, Peiris’s research helped “support the bat origin of SARS-CoV-2”:

When asked how their discoveries affect people’s understanding of the cause of COVID-19, Yuen explained that since he and his team discovered in 2005 that the horseshoe bat was the natural animal reservoir for the ancestral SARS-CoV-1, they believe that SARS-CoV-2 “also went from bats to another mammal(s) before jumping into humans.”

Moreover, SARS-CoV-2 replicates very well in both bat and human intestinal organs, which further supports the bat origin of SARS-CoV-2, he said.

FDA & Big Pharma Conflicts of Interest or Corruption?

big pharma, media, fda conflict of interest
Some might see people on the FDA as having conflict of interest.  The unfortunate thing because for everyone "the sheep" it's business as usual.

Did China Steal IP From NIH Lab & Experiment in Wuhan?

Jim Jordan - Fauci knows his fingerprints may be on covid through NIH lab funding.  Why were U.S. scientists so quick to dismiss the possibility of bioengineering as the potential origin of the Covid-19 virus?  Dr. Fauci is responsible for the funding of 11 NIH labs. Dr Fauci dissembled or tried to hide his long-time support for ‘gain-of-function' research which creates super-viruses that jump from animals to humans. 11 labs in the US create these super-viruses in the US and one of them collaborated with Wuhan Virology Inst —Fauci has supported NIH funds for all these labs!  OR did China steal IP from our NIH labs & they’ve been experimenting with it in Wuhan?


People Injured By COVID-19 Jab Share Their Horror Stories

People Injured By COVID-19 Jab Share Their Horror Stories

At the end of June 2021, Wisconsin Sen. Ron Johnson held a news conference with families who shared stories about the injuries they’d suffered as a result of taking the COVID jab. You can watch the hour-long meeting, which was widely censored and suppressed, above.

While Johnson is diplomatic, stating that most people have no problem after taking the jab, and that the shots have saved many lives, it seems clear that side effects from the COVID injections are FAR more common than anyone is willing to publicly admit.

Case in point: September 10, 2021, WXYZ-TV Channel 7 posted a request on Facebook,1,2 asking people who had lost an unvaccinated loved one to COVID-19 to contact them for a story.

As of September 29, 2021, the post had more than 244,000 comments, and the vast majority are about someone who was injured or died from the COVID shot, or who got severe COVID-19 despite being fully vaccinated. You can browse through the hundreds of thousands of comments here. Below are some examples of the comments posted on the site:

“My good friend’s grandpa just passed away due to receiving his booster vaccine.”

“How about doing a story about my uncle who was in fine shape until he got vaccinated. Or my boss’s uncle who was healthy and in his 50s, then died suddenly a week after getting vaccinated.”

“My sister-in-law’s father died of a stroke 48H after Moderna vax. He was active and healthy.”

“What about my husband’s boss who had two strokes after her second dose?! Not interested in that story?”

“The shot murdered my friend three weeks after he got it.”

“I have a close friend that now has myocarditis after the shots. High Mortality within 5 years. Perfectly healthy prior to the shots.”

“I know 2 women who had strokes right after their shot.”

“We lost an uncle to heart inflammation 2 days after he received the vaccine.”

“Lost a very dear man after his second dose of the vaccine and he said he regretted getting it and he advised me not to get it. How about reporting on those? He died of a brain aneurysm, and was a very healthy man.”

“My beautiful mother passed away recently, 23 days after having the first AstraZeneca shot (that I didn’t know she was getting). ‘Immunization’ was the ‘cause of death’ on her death certificate.”

“I now know more people injured by the vaccine than people who even had covid.”

“No but I know of two people who died from Covid after being fully vaccinated.”

“My uncle passed away 3 months after his second shot. He was diagnosed with stage 4 colon cancer, had surgery, was released to rehab and then died of a blood clot. Thanks Pfizer.”

“I know two women who had miscarriages within 2 days of taking it.”

These responses are what you would call a major CLUE. As noted by one commenter, “Doesn’t sound like you’re getting the story you need judging by the vast majority of these comments about vaccine losses and side effects. Since there is such an overwhelming outpouring of vaccine reactions maybe do a story on that? There’s lots of people here to pool from it seems.”

We now also have medical insiders blowing the whistle, confirming COVID jab injuries are incredibly commonplace, and most are never reported. In an upcoming article, I will share businessman Steve Kirsch’s analysis that strongly suggests the reports in the U.S. Vaccine Adverse Events Reporting System (VAERS) is underreported by a factor of 41. This means there may actually be more than 200,000 deaths and up to 5 million COVID jab injuries.

HHS Whistleblower: ‘Evil at the Highest Level’

In a stunning Project Veritas report, Jodi O’Malley, a nurse working for the U.S. Department of Health and Human Services, reveals health officials are ignoring and covering up COVID-19 vaccine injuries.

O’Malley says she’s seen “dozens of people come in with adverse reactions,” including myocarditis, congestive heart failure and deaths, yet the reactions are not being reported. This, despite the fact that both the U.S. Food and Drug Administration and the U.S. Centers for Disease Control and Prevention require any suspected injury from an emergency use vaccine to be reported.

“If everyone is supposed to gather this data and report it, but no one is reporting it, how will anyone know the vaccine is truly safe? They don’t,” O’Malley says.

 One of the reasons O’Malley decided to come forward, knowing she will likely lose her job over it, is because one of her coworkers who was coerced into taking the shot died. “Nobody should have to decide between their livelihood or take the vaccine,” O’Malley says.

She also points out that while there are medications such as ivermectin and hydroxychloroquine that have been shown to be safe and effective against the virus, the HHS will terminate anyone who uses these drugs. Were these drugs permitted, the COVID jab wouldn’t even qualify for emergency use. When O’Malley asks Gayle Lundberg, a DHHS pharmacist, if ivermectin can be given to a patient if the doctor is willing to prescribe it, Lundberg responds:

“I am stuck. I am told you are absolutely not to use [ivermectin] under any circumstances whatsoever for somebody with COVID, unless you don’t want to have a job. I’m not going to lose my job over this.”

“This is evil at the highest level,” O’Malley says. “You have the FDA, the CDC, that are both supposed to be protecting us, but they are under the government, and everything we’ve done so far is unscientific.”

Another whistleblower, Deborah Conrad, was recently featured in a Highwire exclusive. Conrad, a physician’s assistant, reveals there’s a complete disregard for the requirement to report COVID jab injuries at her hospital too. I will publish that interview this coming Friday, October 8, 2021.

Johnson & Johnson Officials Caught on Tape

In Part 3 of its COVID vaccine investigative series, Project Veritas exposes the true sentiments of two Johnson & Johnson officials: Brandon Schadt, a Johnson & Johnson regional business lead, and Justin Durrant, a Johnson & Johnson scientist.

Speaking to an undercover Project Veritas reporter over a meal, Schadt admits he does not agree with the push to vaccinate children. “Kids shouldn’t get a f*cking [COVID] vaccine,” he says. “It’s terrible … It’s a kid, you just don’t do that, you know? Not something that’s so unknown in terms of repercussions down the road.”

When asked if we really have no idea what the long-term repercussions are, he replies, “I mean, how could you? Right? There’s nobody who’s 30 years in who said, ‘Hey, I had the vaccine and I don’t have a third eyeball.” When asked if we can trust the media when it comes to reporting on the COVID shots, Schadt states, “In no capacity should we ever trust anything that they say.”

Durrant also doesn’t think babies and young children need the jab, saying “It wouldn’t make that much of a difference” if children are unvaccinated for COVID. That said, he does seem to be onboard with the corporate policy to push the injection on adults, regardless of need or personal beliefs.

He admits that what they’re doing is making life so inconvenient for the unvaccinated that they just give up and get it. Despite that, Durrant tells the undercover reporter: “Don’t get the Johnson & Johnson [COVID vaccine]. I didn’t tell you [that] though.”

FDA Warnings Issued for Janssen, Pfizer and Moderna

In late April 2021, the U.S. Food and Drug Administration added a warning label to the Janssen COVID shot about the risk for potentially serious blood clotting in the brain and other sites, including the abdomen and legs, in combination with thrombocytopenia (low platelet count), particularly among women.3,4 In mid-July, Guillain-Barre syndrome and altered immunocompetence were added to the list of warnings.5,6

In June 2021, Pfizer and Moderna both got warning labels added to their COVID shots as the FDA concluded there’s a “likely association” between the mRNA injections and heart inflammation in adolescents and young adults.7

June 24, 2021, Fierce Pharma reported that “heart inflammation has occurred at a rate of 12.6 per million among those aged 12 to 39, according to the CDC’s Vaccine Safety Datalink.”

Menstrual Problems Emerging as a Widespread Side Effect

One of the side effects that has yet to register on the FDA’s and CDC’s radar is menstrual irregularities among women. According to a September 16, 2021, editorial in The BMJ,9 more than 30,000 reports of menstrual irregularities and vaginal bleeding had been filed with the British Medicines and Healthcare Products Regulatory Agency’s (MHRA) Yellow Card Scheme, which collects and monitors adverse vaccine reactions, as of September 2, 2021.

The editorial was written by Victoria Male, a reproductive immunology specialist at the Imperial College of London. According to Male, the link between these bleeding irregularities and the COVID jabs, irrespective of brand, is a plausible one that warrants further investigation. She writes:
“Menstrual changes have been reported after both mRNA and adenovirus vectored covid-19 vaccines, suggesting that, if there is a connection, it is likely to be a result of the immune response to vaccination rather than a specific vaccine component.

Vaccination against human papillomavirus (HPV) has also been associated with menstrual changes. Indeed, the menstrual cycle can be affected by immune activation in response to various stimuli, including viral infection: in one study of menstruating women, around a quarter of those infected with SARS-CoV-2 experienced menstrual disruption.

Biologically plausible mechanisms linking immune stimulation with menstrual changes include immunological influences on the hormones driving the menstrual cycle or effects mediated by immune cells in the lining of the uterus, which are involved in the cyclical build-up and breakdown of this tissue.”

Assistant professor at University of Illinois at Urbana-Champaign, Dr. Kathryn Clancy, who is researching acute immune activation and menstrual repair mechanisms, told The Defender she’s “dismayed that the research design of [COVID] vaccine trials makes it impossible at this time to actually explore this relationship, and hope drug and vaccine manufacturers in the future take these considerations into account.”

US Reports of Menstrual Irregularities

In the U.S., the Vaccine Adverse Event Reporting System (VAERS) had logged a total of 9,589 reports of menstrual disorders following a COVID injection as of September 17, 2021. Dr. Lawrence Palevsky, a pediatrician, also weighed in on The BMJ article, telling The Defender:
“If we were to follow the scientific method, as it was taught in textbooks (knowing full well there is no longer any adherence to the scientific method), we would immediately see this observation of menstrual cycle changes in tens of thousands of women as a signal, for which necessary questions would need to be asked …

A true adherence to the scientific method would allow for answers to be reported without bias or prejudice for a desired outcome of the results … There is a long list of side effects that the manufacturers of the injection sent to the FDA in the fall of 2020.

Many of the injuries people are reporting after receiving these injections, including bleeding, blood clots, autoimmunity, Guillain-Barré syndrome and many others, are well known to the manufacturers and the FDA but, the powers that be continue to ignore the reports of people presenting with these real-time adverse events, as if they have nothing to do with the injections, at all.

Essentially, they gathered the data in clinical trials but have kept them completely under wraps.”

Palevsky believes the menstrual irregularities reported by women who have gotten the COVID shot may be related to effects from the spike protein that their bodies are now producing.

NIH Funds Study to Investigate Menstrual Irregularities

In early September 2021, the Institute of Child Health and Human Development and the Office of Research on Women’s Health, both of which are part of the National Institutes of Health, announced they will award $1.67 million in grants to five research institutions to investigate the link between menstrual irregularities and the COVID jabs.

Over the next year, researchers at Boston University, Harvard Medical School, Johns Hopkins University, Michigan State University and Oregon Health and Science University, will try to determine whether the menstrual changes are directly linked to the COVID shots, how long the changes last, and what the underlying mechanism is.

The five studies are expected to enroll somewhere between 400,000 and 500,000 participants, according to Dr. Diana Bianchi, director of the Institute of Child Health and Human Development.

There’s also an independent group that is collecting data from unvaccinated women who are experiencing abnormal bleeding patterns after coming into close contact with a COVID jabbed individual. Palevsky and Dr. Christiane Northrup are part of this research group, among others. You can find more information about this project on MyCycleStory.com

Mounting Data Tell a Horrifying Story

In closing, while authorities insist the COVID shots are “safe and effective,” mounting data tell a different story. Not only are the injections losing effectiveness within months, as demonstrated by Israeli data discussed in the video above, VAERS has also received more than 726,960 adverse events reports following the COVID shot, including 15,386 deaths and 66,642 hospitalizations, as of September 17, 2021.

These numbers are so staggering, there’s really nothing that can compare. In nine months, these shots have caused more VAERS reports of injury and death in the United States than all available vaccines over the past 30 years. A similar situation can be seen in the U.K., where 30,305 people have died within 21 days of their COVID shot. And that was just within the first six months of the vaccine rollout.18

In August 2021, Japan’s health ministry suspended the use of 1.63 million doses of Moderna’s injection after finding foreign substances that looked like metal particles in some vials. Then, in mid-September, suspected contaminants were discovered in a particular lot of Pfizer’s injection as well.19 Still, we’re told to just roll up our sleeves and ask no questions. Why?

As noted by Schadt, the Johnson & Johnson employee caught on tape by Project Veritas, the mass vaccination campaign isn’t really about public health, it’s about politics and money. Beyond that, I believe it’s about building the control mechanism needed for the Great Reset. Vaccine passports will allow unelected technocrats to control and manipulate the whole world according to their own whims.

As expected, it doesn’t end with two doses. In Israel, a fourth Pfizer shot is already being rolled out, and the year isn’t even over yet. And all those who took the first two doses will now lose all of their freedoms all over again, until they catch up on the recommended boosters. This is precisely what we can expect to happen everywhere else in the world, where vaccine passports are rolled out.

Freedoms are being tied to being up-to-date on your vaccinations, and once COVID-19 disappears, if ever, they’ll just come out with something else that must be injected into you if you want to work, go to school, travel, shop or live a semi-normal life.

This is what the new biosecurity state is built around. The question is, is that any kind of life? Is that how we want to live? Is this the world we want for our children and grandchildren? If not, we must all do our part and resist mandates, vaccine passports and restrictions based on vaccine status. The good news is, together we can win, because there are far more of us than there are of them.

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