The J&J Covid-19 vaccine is being manufactured by the anthrax vaccine company. This is its history
By Dr Meryl Nass, MD | May 19, 2021
Emergent BioSolutions will be in the spotlight today during a House Select Subcommittee Meeting on the Corona Virus Crisis, today at 10:30 am. It can be watched here.
Below, I provide the backstory aka checkered past of this company.
DOD created a plan to vaccinate its service-members against many biowarfare threat agents in the 1990s. At the time, of the bioterrorism vaccines that were being considered, only anthrax and smallpox vaccines had licenses. Anthrax vaccine was chosen to initiate the program in March of 1998.
The first 2 million doses of anthrax vaccine came from a stockpile that had been made for the US army by Michigan’s state vaccine lab (Michigan Biologics Products Institute). What became known in November 1997, after the FDA performed an inspection, was that most of the army’s 11 million dose stockpile of anthrax vaccine, stored at the Michigan lab, was multiply expired, had been redated, and was contaminated, with visible bacterial and fungal growth in some of the lots. FDA immediately shut down the anthrax vaccine factory, and quarantined 9 million of the 11 million existing doses. Unfortunately, FDA allowed the Defense Department to use 2 million doses, which it did over the next two years.
The Conclusions from FDA’s 1998 and 1999 inspection reports of the facility can be read here.
The Michigan state lab was a massive affair with many buildings on a campus in downtown Lansing. It produced a large variety of vaccines and blood products for the state of Michigan. However, over the years the state had not made the required repairs and updates. After the 1997 FDA inspection, Michigan had to repair the place or close it. Michigan decided to sell, and looked for a buyer.
The former head of the Joint Chiefs of Staff, Admiral William Crowe, heard about the sale. He had come to know the el Hibri family when he was Ambassador to the UK. The el Hibri’s had purchased anthrax vaccine from the UK government laboratory at Porton Down just before the Gulf War, and resold it to the Saudi government at a 100x markup.
Crowe and the el Hibri family joined with several of the lab’s officials, and the newly formed group purchased the lab. The purchase price was about 19 million dollars. Admiral Crowe was given a 13% share in exchange for his role as Chairman of the Board, risking none of his own funds. Much of the cost was later paid by the transfer of vaccines to the state of Michigan.
The new company, formed in the first half of 1998, was named Bioport. It chose to focus on its sales of anthrax vaccine to the Army. However, the new company was deeply concerned about potential liability for the lab’s products. The purchase was delayed until the Secretary of the Army signed an indemnification for injuries that might result from use of anthrax vaccine in soldiers, and it also indemnified the company against claims if the vaccine failed to provide the expected protection against anthrax. The state of Michigan had also been indemnified by the Army to produce the vaccine. But from its 1970 licensure until 1998, almost all the anthrax vaccine had only been used in animal experiments.
After FDA had shuttered the anthrax vaccine plant for manufacturing defects, the Army paid to bulldoze and then rebuild the factory in 1999. But even after it was rebuilt, FDA withheld its approval, and the plant lay idle.
Meantime, the 2 million doses that FDA had failed to quarantine were injected into 500,000 military service-members between 1998 and 2001. Many thousands became ill. An official report on the program, quoting unnamed government officials, claimed that 1-2% of recipients had developed permanent disabilities. The military vaccinations were mandatory, and refusers were punished with a court martial or loss of a month’s pay and performance of extra duties. Nonetheless, seeing the injuries sustained by their colleagues, many refused.
In 2001, the anthrax vaccine label, a legal document that describes what is known about the product, listed the CDC’s definition of Gulf War syndrome as a possible adverse effect of the vaccine. (It has been removed from the current label.)
Five Congressional hearings were held throughout 1999 on different aspects of the anthrax vaccine program by the House Committee on Government Reform and National Security (now known as the House Committee on Oversight and Reform). Additional hearings held by other Congressional committees also touched on the vaccine program. The Government Reform and National Security Committee wrote up its findings in a report titled Unproven Force Protection. Its June 30, 1999 hearing dealt specifically with Bioport and its sole source contracts.
Despite this, Bioport has been very successful. Although the Pentagon was considering an end to the anthrax vaccine program in the summer of 2001, the sudden appearance of the anthrax letters after the September 11, 2001 attacks breathed new life into the vaccine program and turned Bioport’s fortunes around. DHHS Secretary Tommy Thompson announced in November 2001 that the anthrax vaccine plant would finally receive an FDA approval and begin production. At the end of January 2002 that is what happened.
But that was not the end of Bioport’s problems. Soldiers challenged the legality of the vaccine’s license in federal court. It was learned that while there had been efficacy testing of an earlier version of the vaccine, the current vaccine formulation had never undergone either efficacy or safety testing in a clinical trial. Aware of this major omission, FDA had withheld the issuing of a “final rule and order” for the anthrax vaccine for over thirty years.
The soldiers prevailed on the legal issues, and First District Court Judge Emmett Sullivan rescinded the vaccine license in 2004, based on the company’s failure to prove efficacy or meet basic FDA standards for licensure.
Unwilling to bow to judicial authority, the Defense Department rolled out a backup plan. A new regulatory authority had just been created, the Emergency Use Authorization (EUA). An EUA was slapped on the unlicensed anthrax vaccine, and DOD quickly restarted its mandatory vaccinations. (There was no emergency: the issuing of an EUA required only the potential for an emergency.)
The attorneys for the soldiers took the case back to court, and Judge Sullivan ruled that even if an experimental medical product received an EUA, it was still investigational and could not be mandated. The law required that EUA products be offered with informed consent. To receive an EUA (unlicensed) product, the recipient must be apprised of the risks and benefits of the product, be informed of alternatives to the product, and no coercion in any form could be applied. Ergo, no mandate.
FDA waited about 18 months, and then issued a full license for Bioport’s anthrax vaccine, although there were still no efficacy data. FDA instead claimed that a 1950’s era trial of a very different anthrax vaccine was sufficient for licensure, even though that trial failed to show benefit against inhalation anthrax.
When the soldiers and their attorneys challenged the licensing decision in court, the next judge ruled in favor of FDA on the basis of “deference”—meaning that FDA could ignore its own regulations when making a determination on safety and efficacy, with or without acceptable data. In 2006 mandatory vaccination restarted.
Bioport then shed its old skin in an attempt to leave its baggage behind. It renamed itself Emergent BioSolutions. Its vaccine had been renamed BioThrax.
Emergent BioSolutions (EBS) then branched out, buying other companies, primarily those making other sole source biodefense products. The military continued to mandate anthrax and (in 2003) smallpox vaccines for service-members. Eventually EBS purchased the smallpox company as well, and the cholera and typhoid vaccines used in the US.
A 2010 report on Emergent BioSolutions, written by Scott Lilly for the Center for American Progress, was titled, “Getting Rich off Uncle Sucker.” It revealed 300% profit margins, unique for a government contractor.
The company’s business plan was to rely on insiders to sell sole source biodefense products to the US government, most of which were stockpiled and never used–inking contracts with multiple federal agencies, including CDC, DOD, NIAID, the State Department, ASPR and BARDA.
In 2012 EBS got one of three DHHS contracts to house a so-called Center for Innovation in Advanced Development and Manufacturing (CIADM) that could be used to produce pandemic or biodefense products in the event of emergencies. With this grant EBS purchased and expanded what became its Bayview factory in Baltimore. The CIADM contract essentially guaranteed Emergent a big role in any future pandemic response.
Emergent acquired the maker of Narcan nasal spray, the opioid overdose antidote. Soon FDA began recommending to prescribers that they write a Narcan script whenever they wrote a narcotic script, just in case. States started buying large quantities for free distribution. Sales rose 600% after EBS bought the company.
Under the Trump administration, retired Air Force Colonel, physician and biodefense consultant Robert Kadlec was appointed to the position of Assistant Secretary of DHHS for Preparedness and Emergency Response (aka ASPR). Kadlec had also been a consultant and business partner of EBS’ founder and chairman Fuad el-Hibri. Kadlec had omitted this information from the required disclosures for Senate confirmation. Once confirmed as Assistant Secretary, Kadlec was able to transfer responsibility for the National Strategic Stockpile (containing the US stockpiles of pandemic remedies, masks and equipment) from the CDC to his own agency. Kadlec then gave multiple sweetheart deals to EBS, until the value of EBS’ contracts with ASPR exceeded those of every other contractor.
ASPR Kadlec was blamed for cancelling a federal contract to make N95 masks while buying more and more anthrax and smallpox vaccines, pre-Covid.
Covid-19 presented a huge opportunity for Emergent BioSolutions. EBS received $628 million from DHHS to retool its CIADM factory. It inked additional contracts with the Astra-Zeneca, Johnson and Johnson, Novavax, Providence Therapeutics and VaxArt companies to provide bulk manufacturing of their vaccines in its Baltimore facilities. Altogether its pandemic contracts were worth about $1.5 Billion. It was slated to manufacture 9 separate medical products to address Covid-19, all designed by other companies.
But there were serious potential problems.
While it had a storied Board of former federal officials, Emergent BioSolutions had never brought a single product to market. Its expertise was in contracting and acquisitions, not production. It had a history of production failures, and had demanded that the federal government bail the company out, or else the sole source products the company provided would become unavailable. Some of this was detailed in the Congressional report Unproven Force Protection. Entering the pandemic, EBS was still making the same mistakes it had been guilty of twenty years earlier:
- EBS sold and continues to sell nerve gas auto-injectors to federal agencies which have been defective and are not licensed. According to the law, these products can neither be produced in the US nor sold here. Instead, Emergent manufactures them in Germany and restricts its sales to US embassies overseas.
- In July 2020, the Soligenix company requested arbitration against Emergent BioSolutions, claiming a loss of $19 million, because EBS had manufactured its experimental ricin vaccine, used in a human trial, which failed to meet specifications.
EBS did not have an active workforce in Baltimore. On September 30, EBS held an online job fair which it titled “Warp Speed Careers Event.” The event sought to recruit 300 employees. Yet EBS had begun inking vaccine contracts 5 months earlier, and could have hired and trained a workforce that was ready to go when FDA gave it the go-ahead. Instead, doing things on the cheap, EBS hired late, failed to provide adequate training to its employees, and experienced a spectacular series of production failures. Many millions of doses of its Johnson and Johnson and its Astra-Zeneca Covid vaccines had to be dumped. J and J missed its 20 million dose quota for the end of March, and FDA, despite repeated inspections, would not give the plant an authorization so its products could be used.
Despite this, somehow millions of doses produced in the unauthorized plant were shipped to Canada, the European Union, South Africa and Mexico. The EU, at least, used the product. How did that occur? We don’t know. Did any get distributed in the US? We can’t be sure none did.
On April 4, 2021, EBS announced it would receive an additional $23 million from DHHS for new equipment to use in the manufacture of Johnson and Johnson’s Covid-19 vaccine.
As of last week, EBS was facing another lawsuit from its shareholders, and its stock price had fallen to $60 from the peak on February 12 of $125 per share. However, Emergent CEO Robert Kramer exercised his stock options in January and February, near the stock’s peak, earning himself over $7 million dollars in profit.
In summary, EBS, despite considerable manufacturing shortcomings, has been extremely successful at obtaining government contracts and earning huge profits. But its products have repeatedly been unreliable. The company has managed to turn failures into success, especially when its products, like civilian stockpiles of anthrax and smallpox vaccine, and nerve gas auto-injectors, are stockpiled but not used.
The public has only gradually been learning that the vaccines it thought were being produced by huge Pharma companies Astra-Zeneca and Johnson and Johnson were in fact being manufactured by the anthrax vaccine company, Emergent BioSolutions. How did it come to pass that the federal government, and these established pharmaceutical companies, bet the farm on EBS’ production of Covid-19 vaccines?
How the CDC is manipulating data to prop-up “vaccine effectiveness”
New policies artificially deflate “breakthrough infections” in the vaccinated, while old rules continue inflating case numbers in the unvaccinated.
By Kit Knightly | OffGuardian | May 18, 2021
The US Center for Disease Control (CDC) is altering its practices of data logging and testing for “Covid19” in order to make it seem the experimental gene-therapy “vaccines” are effective at preventing the alleged disease.
They made no secret of this, announcing the policy changes on their website in late April/early May, (though naturally without admitting the fairly obvious motivation behind the change).
The trick is in their reporting of what they call “breakthrough infections” – that is people who are fully “vaccinated” against Sars-Cov-2 infection, but get infected anyway.
Essentially, Covid19 has long been shown – to those willing to pay attention – to be an entirely created pandemic narrative built on two key factors:
- False-postive tests. The unreliable PCR test can be manipulated into reporting a high number of false-positives by altering the cycle threshold (CT value)
- Inflated Case-count. The incredibly broad definition of “Covid case”, used all over the world, lists anyone who receives a positive test as a “Covid19 case”, even if they never experienced any symptoms.
Without these two policies, there would never have been an appreciable pandemic at all, and now the CDC has enacted two policy changes which means they no longer apply to vaccinated people.
Firstly, they are lowering their CT value when testing samples from suspected “breakthrough infections”.
From the CDC’s instructions for state health authorities on handling “possible breakthrough infections” (uploaded to their website in late April):
For cases with a known RT-PCR cycle threshold (Ct) value, submit only specimens with Ct value ≤28 to CDC for sequencing. (Sequencing is not feasible with higher Ct values.)
Throughout the pandemic, CT values in excess of 35 have been the norm, with labs around the world going into the 40s.
Essentially labs were running as many cycles as necessary to achieve a positive result, despite experts warning that this was pointless (even Fauci himself said anything over 35 cycles is meaningless).
But NOW, and only for fully vaccinated people, the CDC will only accept samples achieved from 28 cycles or fewer. That can only be a deliberate decision in order to decrease the number of “breakthrough infections” being officially recorded.
Secondly, asymptomatic or mild infections will no longer be recorded as “covid cases”.
That’s right. Even if a sample collected at the low CT value of 28 can be sequenced into the virus alleged to cause Covid19, the CDC will no longer be keeping records of breakthrough infections that don’t result in hospitalisation or death.
From their website:
As of May 1, 2021, CDC transitioned from monitoring all reported vaccine breakthrough cases to focus on identifying and investigating only hospitalized or fatal cases due to any cause. This shift will help maximize the quality of the data collected on cases of greatest clinical and public health importance. Previous case counts, which were last updated on April 26, 2021, are available for reference only and will not be updated moving forward.
Just like that, being asymptomatic – or having only minor symptoms – will no longer count as a “Covid case” but only if you’ve been vaccinated.
The CDC has put new policies in place which effectively created a tiered system of diagnosis. Meaning, from now on, unvaccinated people will find it much easier to be diagnosed with Covid19 than vaccinated people.
Consider…
Person A has not been vaccinated. They test positive for Covid using a PCR test at 40 cycles and, despite having no symptoms, they are officially a “covid case”.
Person B has been vaccinated. They test positive at 28 cycles, and spend six weeks bedridden with a high fever. Because they never went into a hospital and didn’t die they are NOT a Covid case.
Person C, who was also vaccinated, did die. After weeks in hospital with a high fever and respiratory problems. Only their positive PCR test was 29 cycles, so they’re not officially a Covid case either.
The CDC is demonstrating the beauty of having a “disease” that can appear or disappear depending on how you measure it.
To be clear: If these new policies had been the global approach to “Covid” since December 2019, there would never have been a pandemic at all.
If you apply them only to the vaccinated, but keep the old rules for the unvaccinated, the only possible result can be that the official records show “Covid” is much more prevalent among the latter than the former.
This is a policy designed to continuously inflate one number, and systematically minimise the other.
What is that if not an obvious and deliberate act of deception?
Steven Crowder gives YouTube legal notice, intends to seek injunction against deplatforming

By Tom Parker | Reclaim the Net | May 17, 2021
Comedian Steven Crowder has announced that last Thursday (May 14, 2021), his company, Louder with Crowder LLC, gave a legal notice to YouTube announcing its intent to file a lawsuit and seek an injunction to stop YouTube deplatforming his channel.
Crowder has one of the most popular conservative channels on YouTube with more than five million subscribers. However, over the last few months, YouTube has removed his videos, demonetized his channel, and most recently, suspended him from uploading or live streaming for two weeks.
“Once we hit the new year and a new president ascended, the landscape of social media shifted in favor of the left,” Louder with Crowder’s editor at large, Courtney Kirchoff, noted in a blog post announcing the legal action against YouTube. “Democrats took control of the presidency and now have control of both houses of Congress. As such, YouTube and other Big Tech platforms feel emboldened, with very few lawmakers standing in their way.”
In a video about the legal action they plan to take against YouTube, Crowder and his lawyer Bill Richmond discussed how the channel is now just one strike away from being deleted after receiving a warning strike and two hard strikes this year.
The warning strike was issued on a coronavirus lockdown anniversary video where someone in the studio said “young children are more likely to die of the flu than COVID.”

The statement reflects Centers for Disease Control and Prevention (CDC) statistics but YouTube deemed the video to be in violation of its “medical misinformation” policy.
“It is tantamount to saying that no conservatives or people who cite the CDC and believe that relevant information like young children have a different immune response to COVID than the standard flu, and it is significantly less lethal to young people but more lethal to old people, which we’ve always talked about, YouTube is saying anyone with that point of view is not welcome on this channel, on this platform, I guess,” Crowder said when discussing this warning strike.
The first hard strike was issued on a March 29 video where Crowder provided examples of a vote being cast from a fake address in Nevada in 2020. YouTube deemed this to be “content that advances false claims that widespread fraud, errors, or glitches changed the outcome of the 2020 U.S. presidential election.”

Crowder said he didn’t make any such claims and described this first strike as “investigative journalism being a violation of the policy if someone doesn’t like it.”
The second hard strike was issued on a May 10 video where Crowder described the Columbus police shooting of Ma’Khia Bryant as “an example of a justified police shooting” that was “necessary to save the life of someone who is in the process of being stabbed.”
According to YouTube, this video violated its rules around “content reveling in or mocking the death or serious injury of an identifiable individual.”

Crowder noted that Big Tech platforms allowed posts that were favorable to Bryant and critical of the police officer to remain up. But when he challenged the criticism of the police officer and argued that the shooting was justified because she had a knife in her hand and was about to swing at another girl, his video was removed and he was suspended.
“That means that the lie is allowed and the truth is not because the truth is simply from a point of view which is impermissible,” Crowder said.
“It’s an incredible indictment of how YouTube enforces its policies and, and really the reason why we’ve had to give the notice, serve the notice of moving for an injunction, to prevent the deplatforming,” Richmond added.
Richmond continued by discussing how he and Crowder’s team are concerned about YouTube actively looking for violations that aren’t actually violations and explained that this is why they’ve moved forward with this injunctive notice which will request immediate relief to protect the existence of Crowder’s YouTube channel.
“This is something that concerns every person who values any type of democracy,” Richmond added. “What they’re saying is ‘these ideas are so dangerous that we can’t address them and rebut them, we can’t criticize them, we just have to extinguish the opinions entirely, we have to eradicate these opinions from the planet because we can’t deal with them.’ But the reality when everyone looks at this is, this is a comedy show that takes on important issues. Commentary, politics, issues that are facing everyone in every part of the nation in the world. And we have to be able to talk about them.”
We Won! Trader Joe’s was the First Crack in the Armor
By Allan Stevo | Lew Rockwell | May 17, 2021
For more than a year, Trader Joe’s has been a particularly troubling store for some readers of these pages.
Trader Joe’s has some excellent quality products at a consumer friendly price with a quirky corporate style. What’s not to like about such a place?
When corona communism was implemented after the Ides of March 2020, we saw exactly what was not to like about such a place.
Trader Joe’s became one of many private companies that enforced the terrible one-sized-fits-all health mandates, including the CDC’s April 3, 2020, face mask order, the single most powerful tool of 2020.
The very concept of private property is further perverted when such behavior takes place as private companies enforce illegitimate government edict.
It didn’t stop there. Through participation in trade organizations, the executives of Trader Joe’s and other companies, called for even more stringent across-the-board policies from government. They didn’t just enable, they didn’t just enforce, they didn’t just encourage, they demanded even more tyranny!
To the credit of Trader Joe’s, their corporate policy always left room for individual exemptions among customers. However, in practice, this was very difficult to invoke. The Trader Joe’s horror stories are legion, and some of the worst of the past year.
In some locations, a customer practically had to have a law degree to get their face mask exemption policy honored.
The easy breezy decentralized corporate style of Trader Joe’s quickly devolved to utter tyrrany as managers were more likely to follow the directives of the CNN chyron than the actual corporate policy.
That once friendly “crew member” who always gave you an extra big smile at checkout was suddenly a mask Nazi of the tallest order.
I mean it when I say “Nazi.” A defining characteristic of nazism was the fusion of state and corporate power. Nazis needed corporate cooperation for their efforts to take hold, just as the corona communists of the Ides of March 2020 did.
Executives at Trader Joe’s overwhelmingly looked the other way as stores enacted the most preposterous policies.
Example: an employee polling other customers on whether a medically exempt customer looked like someone who should be medically exempt from a mask and then inciting customers to corner and angrily confront the unmasked shopper about that.
This kind of sick behavior was happening to grandmothers! Who could possibly justify an employee cornering a shopper in the spices section and gathering together an angry mob of customers?
Regional Vice Presidents encouraged the tyranny further, giving full support to such behavior and being so full of hubris as to actually put such support in writing. That level of hubris speaks volumes about an organization in a way little else can. There was utter disconnect from reality and total contempt for anyone who disagreed. As is so often true, pride precedes a fall.
On April 29, 2021, I sent a strongly worded letter on this topic of their rampant abuse of costumers to Trader Joe’s CEO Daniel Bane.
Just to make sure the letter was not ignored, my team and I followed up that letter with a press release further pointing to Trader Joe’s illegal and unethical discrimination.
It is the job of corporate communications departments to take note of the chatter about their company in the media and online. In such an environment, press releases can be a helpful exclamation point on a sentence that needs to be spoken with emphasis: Don’t tread on us.
If done right, both the CEOs office and the communications team end up going frantically through the company figuring out how to address those concerns.
This particular press release was picked up and reprinted by at least 109 media sources that day. The Trader Joe’s communications team probably noticed.
Beginning the very next day, the toughest Trader Joe’s stores in the country stopped their ridiculous level of radical enforcement. More than a year’s worth of the most unceasing awful behavior toward customers literally stopped overnight.
It was so rampant that I used to receive several complaints about Trader Joe’s some weeks. As of April 30, more than two weeks ago, I have not received a single new complaint. This was not only what I was observing through correspondences, but my team and I also have folks patrolling the world as health freedom inspectors keeping an eye on tyrannical corporate enforcement of illegitimate government policy. These health freedom inspectors reported similar results. Additionally, I myself am constantly out testing techniques and probing for cracks in the system. I firsthand observed an absolute night and day shift on April 30, repeatedly confirmed in the days thereafter.
I think we had their attention.
In the days ahead, I encouraged people to reach out to the Trader Joe’s CEO at his personal email address as follow up to the letter.
Hundreds of readers of these pages did that. This activity peaked with some 300 emails being sent to the CEO on a single day, Thursday, May 13, 2021.
I was CC’d or BCC’d on about a hundred of them that day.
This wasn’t sent to info@traderjoes.com. This was sent to the CEO. 300 emails to a single inbox can be hard to ignore.
The CDC adjusted their guidance on Thursday as well. Trader Joe’s didn’t leap to the lead on that, sticking their necks out because of the CDC guidance. Based on anecdotal accounts, they had a lot of pressure from employees and customers alike. The lawsuits, the complaints, the pushback, the pressure means a lot. I’ve never worked at a company where a single email that was written right and directed to the right inbox at the right time could not move an entire company to immediate action.
Just one email can do that. Anyone who wants to deny that, has never seen that happen or has some agenda by which they seek to discourage you. One, well targeted email can make a difference. Ten can as well. A hundred can. A thousand can. I don’t pretend to know what happened behind the scenes, but I know that our emails had the ability to shape policy at several dozen companies this Friday and my guess is that they did. They may have even helped to shape policy at the CDC, a much harder entity to motivate than a private business. Having seen letters like that cross desks, both governmental and private, I know how very impactful they can be.
What I wouldn’t give to have been a fly on the wall.
The next morning, on Friday, May 14, 2021, Trader Joe’s publicly altered their policy.
They dropped all face mask mandates for customers.
To save face, they cited a CDC guidance from the previous day about vaccines and face masks. They claimed that they would only allow entrance to unmasked customers who had been vaccinated, a detail that they publicly have stated they will not be checking for.
They crumbled.
I knew they were weak, these tyrants, I knew these orders were getting ready to crumble, but I didn’t realize exactly how weak they were. They are very weak and the proper response to weakness from an enemy of freedom is to fight all the harder, until they look back at 2020 and say “I’m never gonna try that again.”
Despite the corporate spin and gobbledygook, the truth of the matter is this:
On May 14, 2021, you and I, who have long been fighting this in ways both big and small, won a decisive victory, as we took down the Trader Joe’s face mask order. We left Trader Joe’s with no other alternative. We made them an offer they couldn’t refuse.
Dozens of companies immediately followed.
This is a huge victory, and it cannot stop here.
Trader Joe’s plans to leave their employees masked. They also plan to keep their “only the vaccinated can be unmasked policy” in place on paper. If allowed to remain in place, it will be only a matter of time before it returns with a vengeance. The next time it is enforced, we shouldn’t expect it to be as generous and easy to defeat as it was this time.
Therefore, we must stop the forced masking of Trader Joe’s employees and we must remove all mention of any government-advised health mandate as a condition of entering a business.
It is not the place of government to place health mandates on us, and it is certainly not the right of corporations to enforce such illegitimate abuses of government power on us. It is illegitimate abuse of government power no matter who enforces it: your neighbor, your grocer, your child’s school, your mailman, or your own mother.
We must truly redouble our efforts.
Time is of the essence. We have a very short window of opportunity to defeat these one-size-fits-all health mandates.
The annual flu season will begin in late-September. Respiratory virus related illnesses and deaths will increase and the fear campaign will intensify. Standard deaths that take place every year from respiratory viruses will be blamed on something scary. “Vaccine” deaths will be blamed on something scary and will certainly not be blamed on vaccines. We will have quite a fight on our hands.
If these one-size-fits-all approaches are still with us and normalized in September 2021, there will be no stopping them. They will be with us a very long time and we really will have entered the new normal. We must return society to normal by the end of this summer, or we risk losing society as we once knew it.
We must roll society back far before 2019, to regain freedoms we were once certain were gone forever, and we must let no vestige of 2020 remain.
That is the work that is ahead of us. That is the work we need accomplished immediately and by September 2021 at the latest, for if we do not, we will go into a far more pernicious battle for our civilization and will be doing so with the forces of freedom so grossly unprepared. That is something we cannot let happen.
I need you to do one thing right now to help me accomplish that, I need you to sign up at RealStevo.com, and I will enlist you in helping me take down these orders. In signing up, you will be joining an army of activists. The army of activists who read my work, who were so responsive, and who hit Trader Joe’s hard and repeatedly made such a difference in shifting this policy. We have much more work ahead of us.
Then I need you to share this article.
With literally 20 minutes of work a day from a dedicated minority, taking targeted action, we can take down these orders.
If you need pointers on how not to wear a mask ever again read my bestselling “Face Masks in One Lesson.” If you would like similar writing free of charge, check out my LewRockwell.com writing on the topic, but really what it comes down to is insisting in your own life that you will live life by a higher standard: that is what saying “No!” to the mask amounts to.
We can do this.
We are winning.
They are desperate.
Victory is at hand.
And now we must close on our victory.
If you’re a closer I need you.
Who is with me?
Report: COVID vaccine adverse effects, huge numbers
By Jon Rappoport | No More Fake News | May 17, 2021
A long-standing private organization, the National Vaccine Information Center, has analyzed the US government’s database, the Vaccine Adverse Event Reporting System (VAERS).
As of May 7, 2021, VAERS lists 192,954 adverse-event reports associated with COVID vaccines. [1]
These events cover the spectrum from mild transient effects to death.
VAERS has always has multiple problems.
One: Doctors aren’t required by law to report adverse effects. Many of them wouldn’t risk blowback by doing so.
Two: There is no comprehensive effort to determine whether an adverse effect is actually caused by a vaccine.
Three: Patients can make adverse-effect reports—but are often hesitant to do so.
Four: By far the biggest problem is: most Americans aren’t even aware that VAERS exists.
Therefore, on balance, UNDER-REPORTING adverse effects is the primary defect of VAERS.
Many efforts have been made to estimate the degree of under-reporting. These estimates state the VAERS numbers should be multiplied by 10, all the way to 100, to obtain an accurate picture of adverse effects.
Ten times the current number of COVID vaccine adverse effects would equal 1,929,540. A hundred times the current number=19,295,400. Either way, the number is staggering.
The death reports are escalating by the day. As of May 7—4,057.
Here are other very troubling categories of VAERS adverse effects, as of May 7. Permanent Disability=2,475. Doctor’s Office Visit=32,801. Emergency Doctor/Room=25,566. Hospitalized=11,538. Birth Defect=112. Life-Threatening=3,548.

Yet, public officials and news outlets continue to repeat the mantra, “safe and effective,” and urge everyone to take the shot.
Every person who receives the vaccine is supposed to be informed of the risks beforehand. I assure you NO ONE is being given these adverse effect numbers, plus the advice to multiply the numbers by 10 or 100.
Lack of informed consent runs contrary to every medical code.
I can also assure you the FDA, which is considering whether to give full approval to the current COVID vaccines, isn’t multiplying the adverse-effect numbers by 10 or 100.
Here is something else to consider. Even multiplying the VAERS numbers by 100 may not be sufficient, because the RNA COVID shots are employing a new technology which a) has never been used on the public before and b) isn’t a vaccine at all; it’s a genetic treatment.
As I’ve shown in recent articles, the entire field of genetic research is riddled with lies, pretense, and unpredictable ripple-effect consequences. The notion of inserting a single genetic change into a person and limiting its effects to an announced goal is a fiction. Unexpected changes occur. And their negative disruptive effects, long-term, are unknown.
Those effects will never be listed in any database.
SOURCE:
[1] https://www.medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=CAT&EVENTS=ON&VAX=COVID19
NED ‘regime change’ specialists claim credit for Belarus protests, boast of funding Russian opposition during prank call

RT | May 17, 2021
A pair of notorious Russian pranksters posing as leading Belarusian opposition figures have duped the National Endowment for Democracy (NED) into revealing the extent of US involvement in Eastern European political movements.
In a video call posted on the online channel of pranksters Vovan and Lexus, senior representatives of the American agency disclosed that they have actively financed and supported anti-government campaigns in the region. The officials from the NED, which is funded by Congress and describes its role as “supporting freedom around the world,” also revealed that they are coordinating efforts with prominent political activists in a range of countries, including Russia.
The officials believed they were talking to Svetlana Tikhanovskaya, the figurehead of Belarus’ opposition movement, and one of her advisors.
During the call, Nina Ognianova, who oversees the NED’s work with local groups in Belarus, outlined the wide-ranging programs the agency bankrolls in the country, insisting that “a lot of the people who have been trained by these hubs, who have been in touch with them and being educated, being involved in their work, have now taken the flag and started to lead in community organizing.”
Ognianova claimed that, through this work, the NED played a role in igniting the colossal street protests that rocked Belarus after long-time leader Alexander Lukashenko declared victory in the country’s presidential election last August. The opposition and many international observers say the vote was rigged in his favor, and tens of thousands took to the streets for demonstrations each weekend after the election.
“We believe that this long-term trust-building that we have had with partners in Belarus has indeed brought the events, or the build-up to the events, of last summer,” Ognianova stated.
“We don’t think that this movement that is so impressive and so inspiring came out of nowhere – that it just happened overnight,” she added, “but it has been developing and we have our modest but significant contribution in that by empowering the local actors to do the important work.”
Carl Gershman, the president of the US state-backed agency, told the pranksters that Washington-based funding and policy groups were already working with Tikhanovskaya and her team “very, very closely.” He then asked the opposition figure, who fled to neighboring Lithuania after the election, to set out her thinking on the situation “so we can understand what your strategy is… and how we can be helpful.”
The comments are likely to add fuel to Lukashenko’s previous controversial claims that the widespread domestic opposition to his government is being stoked from abroad.
The pranksters also pushed the NED’s top team to outline their current activity in Russia, asking what they were doing to support anti-Kremlin activists. Gershman replied that such initiatives are “obviously incredibly important and we’ve emphasized this, going back to the election in August when the demonstrations were taking place in the Russian Far East, and people were connecting with each other and saying we share the same ideals, so we’re very committed to helping on that, and we will – working with our networks and our institutes.”
One of the duo, claiming to be Tikhanovskaya’s assistant, questioned this, saying, “I know that NED is prohibited in Russia now,” referencing a 2015 government decision declaring it to be an “undesirable NGO.” A number of the group’s senior leadership team began to laugh, with Gershman insisting “that doesn’t matter. We don’t have offices, we’re not like Freedom House or NDI [the National Democratic Institute] and the IRI [International Republican Institute], we don’t have offices. So if we’re not there, they can’t kick us out.”
“But we support many, many groups and we have a very, very active program throughout the country, and many of the groups obviously have their partners in exile,” the fund’s president added. “So we are very active and we can be very helpful on this issue.” He added that they were “of course” in touch with Leonid Volkov, a Lithuanian-based activist frequently described as the chief of staff of jailed Russian opposition figure Alexey Navalny.
Barbara Haig, the deputy to the NED’s president for policy and strategy, also hinted at the potential scale of US funding for political groups, saying, “we have a very ample program in Russia” which “goes even down to the grassroots in provinces – oblasts – outside of Moscow. It is very deep and it is very broad.”
Both she and Gershman expressed concern about Russian military exercises billed to take place alongside Belarusian troops later this year, with Haig asking if the group should be “looking at the deployment of Russian military in the country and how that might be changing over time, and whether we should be raising this with some of our contacts.”
Somewhat ironically, Haig also insisted that opposition groups in Russia are concerned about purported efforts to infiltrate and monitor their activity, saying that “security is a huge issue.” How the NED’s most senior figures came to speak with the pranksters, who kept their cameras turned off and spoke in an unconvincing imitation of Tikhanovskaya’s voice, is unclear.
The pair, whose real names are Vladimir Kuznetsov and Alexey Stolyarov, have previously blagged their way into calls with the likes of Prince Harry, Amnesty International and Turkish President Recep Tayyip Erdogan. However, they have been accused by some Western commentators of disproportionately targeting opponents of the Kremlin, with their comedy gotchas frequently seeking to generate political controversy.
The NED describes itself as a “private, non-profit, grant-making organization that receives an annual appropriation from the US Congress through the Department of State.” It acknowledges that its “continued funding is dependent on the continued support of the White House and Congress,” but states that its own “independent Board of Directors” is in charge of how the funds are spent. The agency insists that its “independence… also allows it to work with many groups abroad who would hesitate to take funds from the US Government.” Representatives of the NED have been approached for comment.
FDA’s last word on the safety of hydroxychloroquine and chloroquine was issued last year/ FDA
By Meryl Nass, MD | May 16, 2021
FDA managed to find 385 adverse event reports for either HCQ or CQ in its FDA adverse event reporting system database, as justification for withdrawing its EUA for the chloroquine drugs.
But there wa something strange about these reports. Only 102 of the 385 reports, or 26%, came from the United States. Why would foreigners be submitting reports of adverse events associated with a chloroquine drug to the FDA, instead of to their own pharmacovigilance system?
According to FDA, “FAERS is a database that contains information on adverse event and medication error reports submitted to FDA.” It is not an international database.
Might FDA have requested that foreign entities submit reports? Might some of those foreign entities have been sites where the HCQ overdose trials were conducted? The big three multicenter overdose trials were Recovery, Solidarity and REMAP-Covid. Page 8 of the FDA report does indicate that some of those patients, for whom adverse event reports were filed, had received excessive HCQ doses. Of a total of 256 reports for which FDA had dosing data, depending where you place the excessive dose cut-off, between 23 and 95 had received high doses.
FDA did a number of different things to suppress the use of hydroxychloroquine. This just happens to be one thing I had not previously reported on.
What else is interesting is that this report was compiled in May 2020. It is attached to a website dated July 2020, ten months ago.
In the intervening 10 months, well over 100 papers have been published on HCQ’s use in Covid. FDA claims, “The FDA’s job is to carefully evaluate the scientific data on a drug to be sure that it is both safe and effective for a particular use…” Yet FDA has ignored this massive amount of accumulating literature on hydroxychloroquine, during which 400,000 Americans died of/with Covid. Why? Willful misconduct?
FDA attempts to stop OTC sales of N-acetyle cysteine, an adjunctive treatment for Covid-19
By Meryl Nass, MD | May 16, 2021
Last July, FDA sent out warning letters to supplement companies, informing them that N-acetyl cysteine (NAC) could no longer be marketed as an ingredient in food supplements, using the justification that it was also a licensed drug.
FDA has concluded that NAC products are excluded from the dietary supplement definition under section 201(ff)(3)(B)(i) of the Act [21 U.S.C. § 321(ff)(3)(B)(i)]. Under this provision, if an article (such as NAC) has been approved as a new drug under section 505 of the Act [21 U.S.C. § 355], then products containing that article are outside the definition of a dietary supplement, unless before such approval that article was marketed as a dietary supplement or as a food. NAC was approved as a new drug under section 505 of the Act [21 U.S.C. § 355] on September 14, 1963. FDA is not aware of any evidence that NAC was marketed as a dietary supplement or as a food prior to that date.
But other drugs, such as Coenzyme Q10 and Vitamin D, are licensed as drugs but also permitted to be sold as supplements. And the federal government’s PubChem website lists many virtues of NAC.
In the case of NAC, it has been available as a licensed drug for 57 years in the US. It is widely used and very safe. Unlike many supplements, it has been extensively studied. Clinicaltrials.gov lists 541 studies for the search term ‘N-acetyl cysteine.’ Why did FDA suddenly decide its OTC use should be restricted?
This is especially troubling as a number of doctors have said it is useful in the treatment of Covid-19, especially during the late, cytokine storm stage, since it works as an antioxidant and a substrate for the production of glutathione. In fact, there is a growing body of literature on its benefits for Covid. Here is just one review.
Last week, Amazon stopped selling all products containing NAC. While no absolutely final decision has been made by FDA regarding NAC, it might be the third effective Covid treatment that the FDA has attempted to suppress, after the chloroquine drugs and ivermectin. Stay tuned.
EPA Updates Its “Climate Change Indicators”
By Francis Menton | Manhattan Contrarian | May 13, 2021
It appears that some time last month the EPA provided a major update of what it calls its “climate change indicators.” The EPA’s web page for this is headed “Climate Change Indicators in the United States,” with the sub-heading “Climate Change Is Happening Now.” The update is an initiative of the Biden administration, now eager to invest a few trillion dollars of your money in new “green” infrastructure, after several years in which the Trump EPA paid no attention to keeping these data up to date. The New York Times reports on the big update on today’s front page, under the headline “Climate Change Is getting Worse, E.P.A. Says. Just Look Around.”
The basic technique here is to propagandize you with every sort of essentially irrelevant anecdotal information, while diverting your attention away from the only indicator of “climate change” that actually counts, which is temperature. After all, if temperatures aren’t going up, it isn’t “global warming.” Here, we have some 54 supposed climate “indicators” — everything from rain to drought to ice to sea level — out of which the things relating to actual temperature are only a handful, and then are buried deep in the midst of all the others, probably in the hope that you will miss them. And moreover, the temperature data are then grossly misrepresented in what has to be an intentional effort at deception.
But let’s start with the official line from the new Biden EPA.
The Earth’s climate is changing. Temperatures are rising, snow and rainfall patterns are shifting, and more extreme climate events – like heavy rainstorms and record high temperatures – are already happening. Many of these observed changes are linked to the rising levels of carbon dioxide and other greenhouse gases in our atmosphere, caused by human activities.
The Times then picks up on the theme by its headline calling for you to “just look around” to determine that “climate change” is happening. The idea is that you can determine that there is “climate change” by observing ice on ponds, or something, without having to bother with those complicated thermometers, let alone sophisticated satellite measurements:
Wildfires are bigger, and starting earlier in the year. Heat waves are more frequent. Seas are warmer, and flooding is more common. The air is getting hotter. Even ragweed pollen season is beginning sooner. . . . [EPA’s indicators] map everything from Lyme disease, which is growing more prevalent in some states as a warming climate expands the regions where deer ticks can survive, to the growing drought in the Southwest that threatens the availability of drinking water, increases the likelihood of wildfires but also reduces the ability to generate electricity from hydropower.
So how about the temperature guys? As you can see, the Times does throw in a couple of references to “heat waves” and “hotter air” in the midst of all the stuff about flooding, ragweed pollen, ticks, and whatever else. What’s missing is any citation or link to any source to support the assertion about actual temperatures. But over at the EPA page, under the heading “U.S. and Global Temperature,” we find the following graph, which is said to have been updated to April 2021:
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That appears rather scary! Everything looks like it is going up sharply with passing time. Check out especially the green line, which is identified as the “lower troposphere [temperatures] (measured by satellite) of UAH.” The green line ends with a steep uptick, leaving it with the latest data point just below a record reached in 2016, and a full 2 deg F above the 1901-2000 average.
Oh, but here is the actual lower troposphere temperature record from UAH, available at the website of Roy Spencer, who is the guy who compiles the UAH record:
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There are a few differences in the presentation that require a little interpretation, like the EPA graph is in deg F and has anomalies from a 1901-2000 mean, while the UAH graph is in deg C and shows anomalies from a 1991-2020 mean. But still, it leaps out that the green line on EPA’s web page, said to be the UAH record, ends with a sharp uptick and with the last point a full 2 deg F above the mean line; while this record, from UAH itself, ends with a sharp downtick and the last point actually below the mean line. Although EPA explicitly says on its web page that it updated the information in April 2021, this downtick in the UAH record began in January 2020 — a year and 4 plus months ago — and reflects a decline in lower troposphere temperatures of some 0.65 deg C, which is almost 1.2 deg F.
In other words, well more than half of the seemingly scary increase in temperature since 1901 shown in the EPA graph has just gone away in the last 16 months. So the Biden EPA, not wanting to complicate the official story of “climate change is happening now,” simply truncated the data in its graph at January 2020 to shut out the last year plus of big temperature declines. There is no way to characterize the EPA graph as other than intentionally deceptive.
I guess it’s OK because it’s in the noble cause of convincing the American people to allow the government to spend a few trillion dollars on windmills and electric car charging stations for the rich.





A Review of Conspiracy Theories and Other Dangerous Ideas by Cass Sunstein (based on an earlier paper co-authored with Adrian Vermeule); In Defense of Troublemakers: The Power of Dissent in Life and Business by Charlan Nemeth; and Conspiracy Theories and the People Who Believe Them, edited by Joseph E. Uscinski