Snake Oil: the most vaxxed country in Europe now has its worst COVID outcomes
Are those two things related?
By Jordan Schachtel | The Dossier | June 29, 2022
Virtually every single adult in Portugal has taken at least two doses of “miracle cure” COVID vaccine, with the vast majority “boosted” as well. Yet this month, the most vaxxed country in Europe has consistently reported its worst outcomes.
Once thought to be the best positioned nation in Europe to deal with future bouts with the coronavirus, a nuclear bomb of reality has hit Lisbon.
Out of all the countries in Europe, “Portugal has experienced the most dramatic wave,” the Guardian reports. “With infections per million remaining at a seven-day average of 2,043 on Monday – the second highest new case rate in the world.”
It appears the “miracle cure” vaccines have not only not failed to curb the COVID issue, but has potentially made it worse.
Study: Boosted People Slowest to Clear COVID-19
That’s why PAXLOVID does not work for them
By Igor Chudov | June 30, 2022
A new study just came out:
It looked at how long “culturable virus” (that is, virus capable of infecting people) is present in Covid patients after the first positive test. The authors literally cultured swabs of patients, on various days past-diagnosis, and counted how many patients, by vaccination status, are still carrying live, replication-competent virus.
The result is shocking:
What this chart shows is that one-third of boosted people still carried live, culturable virus at 10 days after the beginning of the infection. This is contrasted with unvaccinated people, who had only 6% of persons still contagious at Day 10.
This means that the share of boosted people who are still contagious (31%) is over five times greater, than the share of still-contagious unvaccinated people (6%).
In other words: out of 100 boosted persons who catch Covid, fully one-third will be still carrying LIVE VIRUS on Day 10. Out of 100 unvaccinated persons, only one out of 16 would test positive on Day 10 — over five TIMES fewer people.
As a word of warning, the study involved a relatively small amount of people, so statistical significance is probably not quite what we’d like it to be — but it shows what we saw all along in other news.
It also means that boosted people, who might feel better in a few days, would be contagious for a few MORE days after recovery, thus becoming silent superspreaders of Covid. So much for “stopping the spread”!
This is why Paxlovid does Not Work for the Boosted
This study explains why Paxlovid does not work in vaccinated (and boosted) people. For the introduction into my paxlovid series, see the sad story of double-boosted Dr. Fauci, who relapsed on Paxlovid, with links to my Paxlovid articles shown chronologically:
What Paxlovid is, is a biomolecular “snooze button” that suspends viral replication for 5 days. However, as we can see, one-third of the boosted people still carry live virus at 10 days due to delayed, or disabled, immune responses. Those persons would be likely to rebound on Paxlovid.
The numbers also match other calculations: my guesstimate of unvaccinated Paxlovid rebound was 12% — that is not too far from 6% of unvaccinated people in this study who carried live virus on Day 10. 31% of boosted people who still have live virus on Day 10, matches Twitter reports of 40-50% rebound rates in vaccinated people.
In other words, while we had fairly certain evidence that Paxlovid does not work for vaccinated people, and suspected the vaccine, we were missing the most crucial proof: that of live virus not clearing in the boosted. The study I mentioned above, provides this proof.
It also exposes vaccines as merely “increasing tolerance” to Sars-Cov-2, as opposed to generating robust immune response that leads to rapid viral clearance.
Molnupiravir
I personally have not paid close attention to Merck’s Molnupiravir, due to it being a dead-end, mutagenic, cancer-causing, variant-generating, toxic-to-bones drug from hell, which is, fortunately, seeing little use. Our friend Modern Discontent discovered that Molnupiravir is also snake oil and does not work in vaccinated people.
Getting boosted is a great way to become unable to clear a Covid infection in 10 days and become a Covid superspeader.
Setback for US hypersonic program as another test ends in failure
Press TV – July 1, 2022
The latest test of a US hypersonic missile in the state of Hawaii failed on Wednesday, the Pentagon said, attributing the failure to an “anomaly” during the first test of the full system.
The failed test was part of the Conventional Prompt Strike (CPS) program, under which aerospace and military equipment company Lockheed Martin is trying to develop weapons capable of flying at super high speeds for use on submarines and ships.
The test, carried out at the Pacific Missile Range Facility in Hawaii, was supposed to launch the Common Hypersonic Glide Body atop a two-stage missile booster.
The booster is designed to launch the system and accelerate it to hypersonic speeds above Mach 5, at which point the glide body detaches and uses its speed to reach the target. It was the first time the entire system was tested, called an All Up Round test.
“While the Department was unable to collect data on the entirety of the planned flight profile, the information gathered from this event will provide vital insights,” Pentagon spokesman Tim Gorman said in a statement.
He did not provide any additional details on the nature of the anomaly or at what stage of the test it occurred, adding that the Pentagon is currently investigating the reasons for the failure of this missile test.
In October 2021, a similar test failed in Kodiak, Alaska. Despite the failure of both tests, the Pentagon has expressed confidence to develop offensive hypersonic capabilities by the early 2020s.
“Delivering hypersonic weapons remains a top priority and the Department remains confident that it is on track to field offensive and defensive hypersonic capabilities on target dates beginning in the early 2020s,” the Pentagon spokesman stated.
The Pentagon has focused its attention recently on hypersonic weapons development amid concerns that the country could lag behind the Chinese and Russian programs.
China successfully tested a hypersonic weapon last year that orbited the globe before striking its target. Russia has also greatly developed its hypersonic weapons in recent years.
The latest test failure, which was first reported by Bloomberg, has dealt another blow to the US in the race to develop hypersonic missiles.
As West blames Moscow for ‘food crisis’, ships sail from Mariupol with Moscow’s help
Meanwhile Ukraine holds vessels in its ports
By Eva Bartlett | Samizdat | July 1, 2022
Without much notice in the West, on June 21, the first foreign ship departed from the Port of Mariupol since Ukrainian and foreign mercenary forces were fully forced out of the Donbass city a month prior. Escorted by Russian naval boats, the vessel’s departure set the precedent for a resumption of normal port activity to and from Mariupol.
Russia’s Defense Ministry on May 20 announced the liberation of the Azovstal plant from Ukraine’s Nazi Azov Battalion, and some days later stated that sappers had demined an area of one and a half million square meters around the city’s port.
In early June, the ministry declared the facility ready for use anew. “The de-mining of Mariupol’s port has been completed. It is functioning normally, and has received its first cargo ships,” Defense Minister Sergey Shoigu said at the time.
Russia promised to give ships safe passage, and on June 21, the Turkish ship Azov Concord left with a Russian escort. At Mariupol port that day, prior to setting off, the captain of the ship, Ivan Babenkov, spoke to the media, telling us that the vessel, without cargo, was heading to Novorossiysk for loading, and then on to its destination.
Rear Admiral Viktor Kochemazov, commander of the Russian naval base in Novorossiysk on the Black Sea’s northeastern coast, down the Kerch Strait from Mariupol, explained that while the corridor has been operational since May 25, the nearly one-month delay in departing was because “ships were significantly damaged during the conduct of hostilities.” Notably, he also said that some ships were deliberately damaged by Ukrainian forces in order to prevent them from leaving.
From aboard a Russian anti-sabotage forces boat, media watched the Azov Concord leave port. Further on, the ship would be met by warships of the Novorossiysk base and escorted to the Kerch Strait where FSB border control ships would continue to escort the ship.
A Bulgarian ship, the Tsarevna, was readying to depart the port next, “also following the same humanitarian corridor to its destination in accordance with plans for the use of the court by the owner,” Rear Admiral Kochemazov said.
Western press ignoring developments
Predictably, just as the Western media continues to ignore Ukraine’s war crimes against the Donbass republics, including not only the bombing of houses, hospitals, and busy markets – plus the killing and maiming of civilians – so too do they omit coverage of anything positive emanating from areas where Ukrainian forces have been ousted and stability restored.
Instead, Western media continues to spin the story that it’s Russia that’s blocking ports and preventing grain exports, and blame Moscow for “aggravating the global food crisis” – when in reality, it is Ukraine that has mined ports and burned grain storages.
In fact, according to Russia’s Ministry of Defense, “70 foreign vessels from 16 countries remain blocked in six Ukrainian ports (Kherson, Nikolaev, Chernomorsk, Ochakov, Odessa and Yuzhniy). The threat of shelling and high mine danger posed by official Kiev prevent vessels from entering the high seas unhindered.”
While Russia maintains it has opened two maritime humanitarian corridors in the Black and Azov Seas, Kiev is apparently not engaging with representatives of states and ship-owning companies about the departure of docked foreign ships.
Meanwhile, in the same vein, media outlets like the New York Times (writing as always from afar) claim that Mariupol is “suffering deeply” under Russian rule (citing the runaway former mayor, nowhere near the city for months, who is the source of previous war propaganda) even describing the Azov Neo-Nazis as “the city’s last military resistance.”
Yet, what I’ve seen in multiple trips to Mariupol in the past couple of weeks is rubble being removed so that the rebuilding process can begin, newly established street markets, public transportation running, and calm in the streets.
The people of Mariupol have indeed suffered, but now that the Azov Nazis and Ukrainian nationalists no longer reign, they can live without fear of persecution, execution, rape, torture, and all of the other ‘democratic values’ of the forces backed by the West.
The rebuilding will take time, but with the port functioning anew, and the possibility now of also bringing reconstruction materials by sea, it can begin, ship by ship.
Eva Bartlett is a Canadian independent journalist. She has spent years on the ground covering conflict zones in the Middle East, especially in Syria and Palestine (where she lived for nearly four years).
‘Ridiculous’: Russia dismisses claims of NATO being ‘defensive alliance’
Press TV – July 1, 2022
Russian Foreign Minister Sergei Lavrov says the claim of NATO being an exclusively defensive alliance is “ridiculous and disgraceful.”
He made the remarks on Friday while addressing students and teachers at the Belarusian State University, in response to recent statements by a number of NATO members’ officials.
“Recently, a representative of the White House once again reiterated that Russia should not be afraid of NATO and that no one should be afraid of it at all, because NATO is a defensive alliance. But it is already ridiculous to hear adults say such obvious nonsense. I would say, it is simply disgraceful,” Russia’s TASS quoted Lavrov as saying.
Pointing to the history of NATO’s establishment and its confrontation with the Warsaw Treaty Organization and the Soviet Union, he said both the Warsaw Treaty and the Soviet Union are gone but “NATO has moved eastward five times.”
“Who are they defending themselves from then?” he asked rhetorically, adding, “When someone pushes forward, establishes control of territories, and deploys armed forces and military infrastructure there, it is not exactly what is called defense. It’s just the opposite.”
The remarks come as the 2022 NATO Summit in Madrid wrapped up on Thursday with the bloc’s decision to strengthen its forces along the eastern flank while also officially inviting Sweden and Finland, which share borders with Russia, to join the alliance.
“NATO is a defensive alliance and poses no threat to any country,” reads part of the declaration of the Summit.
The declaration also named Russia as a “direct threat” to NATO members’ security, noting that the military alliance “does not seek confrontation and poses no threat” to Russia.
At the same time, it went on to threaten to respond in a “united and responsible way” to any threat from Moscow.
‘Joke of the century’
Chinese foreign ministry spokesperson Zhao Lijian also rejected the notion of NATO being only a defensive alliance.
“NATO is a ‘defensive’ alliance? Joke of the century,” he tweeted on Friday while also sharing a combination of images portraying NATO’s military intervention in several countries such as Afghanistan, Iraq, and Libya.
In a separate tweet, the Chinese official also pointed to the role of the US and its allies in the continuation of the war in Syria and its devastating effects on people’s lives.
“[The] US and its allies continue to fuel the war in Syria. More than 300,000 civilians have died in the conflicts according to UN statistics, 1.5% of Syria’s population,” he wrote on Friday, also sharing a photo of war damages in Syria with a note which read “who is the threat to peace?”
NATO members had also alleged that China poses a “challenge” to the bloc’s “interests, security, and values.”
Speaking in a daily briefing on Thursday, Zhao stressed the futileness of hyping up the so-called “China threat.”
“NATO has extended its reach to the Asia-Pacific region in an attempt to export the Cold War mentality,” he said, urging the bloc to stop making baseless accusations and provocation against China, abandon the outdated Cold War mentality, and stop dangerous acts that disrupt Europe and the Asia-Pacific.
US should pull out of NATO: Rep. Marjorie Taylor Greene
Samizdat | July 1, 2022
Washington should pull out of NATO instead of sending billions of taxpayer dollars to Ukraine and risking a nuclear war, according to a Republican congresswoman who has been highly critical of Washington’s response to the Ukraine crisis.
Georgia Representative Marjorie Taylor Greene, a strong supporter of former President Donald Trump, made the case in a series of tweets on Thursday.
Ukraine is the “new Iraq wrapped up with a pretty little NATO bow, with a nuclear present inside,” she wrote.
“The American people do not want war with Russia, but NATO & our own foolish leaders are dragging us into one. We should pull out of NATO.”
She described the provision of military aid to Ukraine, which she voted against in Congress, as a “proxy war” against Russia that Americans have no appetite for.
“Grinding up Ukraine to fight with Russia is disgusting, they could have been an ally,” she tweeted.
Marjorie Taylor Greene also listed a host of problems that she sees as more pressing for the American people, from soaring inflation to fentanyl overdoses and rampant crime. The only people vying for a conflict with Russia are “those who make money off of it,” she claimed.
“NGOs, defense contracts of all kinds, grants, business deals, even humanitarian aid, political consultants, & more,” she wrote. “War is an industry. A deadly profitable industry.”
Warmongers in Washington seeking war with Russia “should suit up and go fight it” themselves, she suggested. “Send your kids and leave ours alone. Pay for it yourself.”
Alabama is first state to seek ban on gender-affirming treatments for children
Samizdat | July 1, 2022
The state of Alabama has called on a federal court to uphold a ban on so-called gender-affirming medical treatments for transgender youths, citing a recent Supreme Court ruling that allowed state governments to prohibit abortions.
In a 76-page brief filed with the 11th US Circuit Court of Appeals on Monday, Alabama Attorney General Steve Marshall insisted that a previous injunction on the state’s ban of transgender treatments should be overturned, since such care is not protected under the 14th amendment to the US Constitution as it is not “deeply rooted in the nation’s history and traditions.”
“The Legislature determined that transitioning treatments in particular are too risky to authorize, so it is those treatments Plaintiffs must show the Constitution protects,” the brief says. “But no one –adult or child– has a right to transitioning treatments that is deeply rooted in our nation’s history and tradition.”
The state’s argument closely resembles the reasoning behind the recent US supreme court decision to overturn Roe v. Wade, which removed federal abortion protections and placed the responsibility for legalizing or banning the procedure on individual states and their citizens.
Supreme Court judges that ruled in favor of overturning the legislation argued that terminating a pregnancy was not a fundamental constitutional right because it was not explicitly mentioned in the US constitution and was not “deeply rooted in this nation’s history and tradition.”
In the brief, Marshall goes on to insist that the Constitution reserves to the state, and not courts or medical interest groups, the authority to determine that “sterilizing interventions” are too dangerous for minors, adding that the State has a right to regulate or prohibit such interventions for children “even if an adult wants the drugs for his child.”
The Attorney General also noted that research regarding these “novel interventions” was poor and that they were unproven to offer lasting relief to children suffering from gender-related distress. “What research does exist is already outdated – a remarkable fact given that the seminal study on transitioning children was published less than a decade ago and has not been replicated,” he added.
Marshall also drew attention to the fact that gender-related distress has become “a tsunami” as clinics offering “‘transitioning’ treatments on kids are seeing their patient loads increase by thousands of percent,” noting that the new trend was “troubling.”
In April, Alabama governor Kay Ivey signed into law a bill which made it a felony to provide gender-affirming treatments to minors, and sought a 10-year prison sentence and a $15,000 fine for anyone providing puberty blockers, hormones or surgical procedures to transgender youths under the age of 19.
However that legislation was partially blocked one month later by a federal judge, who dismissed the state GOP leader’s claim that puberty blockers were “experimental,” and insisted that transitioning medications were “well-established, evidence-based treatments for gender dysphoria in minors” endorsed by “at least 22 major medical associations.”
South Korea, Poster Child for Containment Strategy, Now Has Same Excess Mortality as Sweden
BY NOAH CARL | THE DAILY SCEPTIC | JUNE 30, 2022
Until recently, South Korea was the poster child for the ‘contain and vaccinate’ strategy, having kept infections to a minimum until completing its vaccine rollout.
In November of last year, former ‘Zero Covid’ proponent Devi Sridhar argued, “It is never too late to learn lessons from countries such as South Korea, which pursued maximum suppression, and succeeded.” And in a super-viral tweet, Vincent Rajkumar (a professor at the Mayo Clinic) proclaimed, “South Korea followed the textbook principles of epidemiology. Kept deaths 40 times lower all the way till 75% of population fully vaccinated. This is success.”
All that was true until February of this year, when the country saw its first major outbreak. This outbreak, as I noted previously, led to a large spike in excess mortality; by March’s end, the number of weekly deaths was almost 70% higher than normal.
Owing to this spike, South Korea now has the same excess mortality as Sweden – which took a famously relaxed approach to dealing with Covid. Note: the chart below is based on weekly deaths, rather than age-standardised mortality rates, so it overstates excess mortality in both countries.
Incidentally, you wouldn’t know this from looking at the official Covid death rates. As the chart below indicates, the number of ‘confirmed’ Covid deaths per million people is much higher in Sweden, presumably due to differences in testing or diagnosis. Which illustrates the importance of tracking excess mortality.
So, the country that did least to contain Covid has ended up with the same death toll as one of the countries that did most. What’s more, the majority of Sweden’s infections occurred before the vaccine rollout, whereas the vast majority of South Korea’s occurred after. Which suggests the benefits of containing the virus until after the vaccine rollout have been overstated.
Of course, South Korea didn’t do terribly. By containing the virus using border controls and contact tracing, they avoided really draconian lockdowns, and saw a comparatively mild downturn. Yet the measures they took still constitute a major infringement on civil liberties. As the Guardian notes, “Koreans’ movements were so finely and publicly tracked that secret love affairs and even hidden sexualities were brought to light.”
Anyone who cares about civil liberties will now have to ask whether South Korea’s strategy was worth it, given that Sweden ended up with the same death toll.
FDA Panel Votes to Waive Clinical Trials for New COVID Boosters
By Megan Redshaw | The Defender | June 29, 2022
The U.S. Food and Drug Administration’s (FDA) vaccine advisory panel on Tuesday voted 19 to 2 to recommend new COVID-19 booster shots that include the Omicron variant this fall.
The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) did not issue guidance on whether additional data would be needed to recommend an updated composition of the primary-series vaccines authorized for emergency use in the U.S., or whether it would be appropriate to continue to use a primary-series vaccine as a booster.
It is the first time VRBPAC has suggested vaccine makers modify their vaccines to target a different variant, according to CNBC, which also reported the FDA will likely accept the committee’s recommendation.
If so, the FDA would be authorizing a vaccine change without requiring additional data showing a bivalent vaccine — containing both the original 2019 Wuhan variant and one of the Omicron variants — is safe and effective for those age groups that are already authorized to receive a booster dose.
The FDA plans to decide by early July whether vaccines will target the now-dominant BA.4 and BA.5 Omicron subvariants or the BA.1 Omicron variant that led to a surge in infections last winter, Reuters reported.
At the beginning of the meeting, Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, suggested a newly designed shot could begin in October, adding that it takes manufacturers around three months to choose a vaccine design and begin producing doses.
Dr. Paul Offit, director of the Vaccine Education Center and professor of pediatrics in the Division of Infectious Diseases at Children’s Hospital of Philadelphia, and Dr. Hank Bernstein, professor of pediatrics at Zucker School of Medicine, were the only two members who broke from the panel to vote against the initiative.
Offit acknowledged there’s a benefit to providing a booster in the fall to some age groups, but questioned whether Omicron was the right strain. He said the move to new-variant vaccines was happening too fast, with too little data.
“I think as a new product it should be handled as a new product,” Offit said. “I think we need a higher standard than what we’ve been given. …“I’m not comfortable enough to support the risk of a new product.”
Bernstein expressed concern over the lack of data used to justify changing the strain, and the potential that by the time a subsequent booster is approved, it will contain outdated strains.
“So, in sum, I think including an Omicron strain in the vaccine seems to have some potential, but data especially for BA.4 and BA.5 are limited at this time, and that’s why I’m struggling to even make a strain change at this time,” Bernstein said.
Bernstein also said he didn’t see a need to change the strain as the current vaccine being used is shown to be effective against severe disease — a claim made just two weeks earlier at a prior VRBPAC meeting.
Bernstein said the strain change would need to be supported by data showing improved vaccine effectiveness and he “didn’t think we really have the data to be able to say that” even though the panel looked at the immune response.
Dr. Ofer Levy, VRBPAC member and an infectious disease physician at Boston Children’s Hospital, voted “yes” to change the computation of COVID-19 boosters, despite Pfizer’s admission there is “no established correlate of protection,” referring to the level of antibodies needed to confer protection.
“You have a lot of data now,” Levy told Pfizer. “What is your relative protection?”
“I would say there is no established correlate of protection,” Kena Swanson, Ph.D., vice president of viral vaccines at Pfizer, told Levy.
Levy circled back during the meeting:
“I would like to hear from FDA what their overall approach will be around improving our understanding of correlate protection. We spend a good amount of time reviewing antibody data. We have no doubt antibody data is important. We don’t have a level of antibody that anybody is comfortable stating is correlated [with] protection.
“So yes, the antibodies are important but so are the T cells. We heard from Dr. Weir, yes, T-cell assays are trickier and they’re more diverse, but it’s not going to happen without federal leadership to have a standardization of the T-cell assay and encourage or in fact require the sponsors to gather that information.”
“So what is the effort to standardize the pre-clinical assays?” Levy asked. “This is an effort that’s critical not just now but for future cycles of vaccine revision. If we aren’t able to define a standard for correlate protection we are fighting with one arm behind our back.”
Marks acknowledged the importance of Levy’s question, but said T-cell-mediated immunity was “difficult to study” initially.
“We have been having conversations with our colleagues at the NIH [National Institutes of Health] and throughout government about how we might move forward here,” Marks said. “It is something that we don’t have an answer to yet.”
Marks said as vaccines are developed in the future, it will “become even more important” to define a standard of correlate protection because “we won’t be able to have a large naive population to vaccinate with newer vaccines.”
“We will need to understand the T-cell response better,” Marks said. “I take your point, it’s just that we haven’t solved the problem yet.“
Dr. Meryl Nass, a member of the Children’s Health Defense scientific advisory committee, told The Defender that in her opinion, Tuesday’s meeting was a “vote to essentially approve a future framework — the future framework being a dearth of evidence required to change the booster, without clinical evidence and without a correlation of protection.”
Nass added:
“They voted on using an Omicron variant in the next booster iteration — which could contain any Omicron variant and could be either mono- or bi-valent.
“But most likely they will keep the current version and add another — which might double the amount of mRNA, or not.”
The new formulation might be for adults alone or adults and children, or only older adults and the immunocompromised, Nass said.
Brian Hooker, Ph.D., Children’s Health Defense chief scientific officer and professor of biology at Simpson University, told The Defender :
“The proposed move by VRBPAC will increase the harm to the U.S. public to unprecedented levels, as this action will further circumvent necessary clinical trials even beyond the slapdash testing of COVID-19 vaccines under Emergency Use Authorization.
“This adds to a foundation of lies used to authorize the original COVID-19 vaccines without anywhere near proper testing.”
Dr. Cody Meissner, VRBPAC panel member and professor of pediatrics at Tufts University, expressed concern about the financial risk pharmaceutical companies “are taking by making these vaccines.”
“If there’s a low likelihood the vaccines will be recommended, then they could incur significant loss,” he said.
Marks responded:
“I guess I would say that I would make recommendations here knowing the vaccine manufacturers will be kept whole by the United States government at least for some vaccines. I could be wrong but I think that’s a reasonable assumption.”
During the meeting, Moderna told the panel it would be ready with a “couple of hundred million” bivalent, or double-targeted, vaccines designed to combat BA.1 by September, but it would be late October or early November if the company needs to design a new vaccine targeting subvariants.
Pfizer said it and partner BioNTech have a significant amount of vaccine doses designed for the BA.1 variant ready and are already preparing to produce a large number of doses targeting BA.4 and BA.5 Omicron subvariants.
Pfizer said either could be ready for an early October rollout.
Multiple concerns raised during the public comment session
During the public comment session of the meeting, experts raised concerns that were largely ignored by the advisory panel.
Dr. Dustin Bryce, with Interest of Justice, said the FDA, Centers for Disease Control and Prevention (CDC) and the World Health Organization are “usurping Congress’ definition of a vaccine — which is any substance designed for the prevention of one or more disease.”
“FDA actually classifies mRNA as gene therapy, which they say is to treat or cure an existing disease by modifying your genes,” Bryce said. “Gene therapies are still being studied and are experimental at this time.”
Citing FDA documents, Bryce said gene therapy, unlike a vaccine, is so inherently unsafe the FDA says it requires 15 years of research to follow up on safety due to known risks of antibody-dependent enhancement, alteration of DNA and delayed adverse effects, such as cancer.
Bryce said:
“FDA says that gene therapy use in the mass population represents an unreasonable risk and they should limit the number of subjects who might be exposed to risk. We require due process and forbid the FDA from authorizing the proposed changes.
“We are demanding that EUA [Emergency Use Authorization] is promptly revoked because unreasonable risks are inherent in gene therapy products, as evidenced by large numbers of reports of adverse serious events linked to or suspected of being caused by an EUA product, product failure and product ineffectiveness.”
Bryce said COVID-19 vaccines fail to meet the requirements of EUA because not a single mRNA vaccine has been found to be effective for the prevention or treatment of an existing disease.
Michael Briskin pointed out in his public comment that the FDA receives approximately 75% of its budget from pharmaceutical companies, which he believes represents a conflict of interest.
Briskin challenged the use of the phrase “safe and effective” to describe COVID-19 vaccines, given the FDA has done no long-term testing to determine whether these products are safe.
Briskin presented data showing a significant rise in reported deaths among working-age Americans following COVID-19 vaccine mandates.
He said:
“In the short-term, 2021 was a very interesting year. We saw a stark increase [in death] among working-age adults from 18 to 64 and specifically in Q3 and into Q4, so something new for the working-age demographic partly through 2021 would be the clear correlation.
“With comparable trends in BLS [Bureau of Labor Statistics] data, children’s health insurance data, Israeli ambulance data, and of course we have the [Vaccine Adverse Event Reporting System (VAERS)] data — which the CDC tried to minimize but a recent FOIA [Freedom of Information Act] request forced them to reveal that they never once did the PRR calcification that was supposed to be their tool for spotting safety signals, according to their posted documents.”
“And what do we do when people get injured from these vaccines?” Briskin asked the panel. “We leave them in the mud.”
Briskin chastised the panel for authorizing boosters for infants two weeks earlier when data showed two doses weren’t effective and only 10 cases were used to assess efficacy.
“Three-quarters of the severe COVID in the trial was in the vaccine arm, as was the only hospitalization case which was accompanied by a seizure,” Briskin said. “And Moderna is so dangerous in young people Nordic countries won’t allow it to be used in anyone under the age of 30.”
Briskin said:
“In fact, the director of health of Denmark just admitted that vaccinating children was a mistake, whereas our officials only ever doubled down. And now we’re about to double down so hard we are about to lose the pretense of holding these pharmaceutical companies to any statistically meaningful regulatory standards for formula modification.
“For people following at home, what this agency is proposing is not just modifying the genetic code in the vaccine and the structure of the proteins produced to chase variants, but even things like doubling the microgram count for Pfizer — all without doing any statistically powered safety studies.”
“And to be clear,” Briskin added, “the companies we’re giving carte blanche to include Pfizer, the world’s largest criminal organization having paid the world’s largest criminal fine, and Moderna, which never made a safe product before we did away with long-term safety testing.”
Dr. Eric Feintuch, a chiropractor, asked the FDA if the agency knows how long mRNA from COVID-19 vaccines and the spike protein stay in the body, whether they know what the rate of protein production is and whether the FDA is aware of the consequences of the methylpseudouridine substitutions at the codon optimization step.
“For anyone on this panel who says it doesn’t go anywhere, tell me what proof you have of that,” Feintuch said, referring to the spike protein.
Feintuch said COVID-19 vaccines are associated with prion disease, noting 26 people have reported experiencing sudden onset of a severe and fatal brain disorder within one month of the second mRNA vaccine dose.
“This information needs to be researched and seen,” Feintuch said.
“A thousand peer-reviewed studies question the safety of COVID-19 vaccines. Doesn’t anyone see the safety signals? Is there anyone here who will stand up?” he asked. “Some of you know this, you need to stand up and you need to help us.”
Dr. David Wiseman, a research scientist with a background in pharmacy, pharmacology and experimental pathology, said VRBPAC is once again being asked to opine on inadequate information.
Wiseman said the FDA recently waived efficacy requirements for COVID-19 vaccines and has ignored its experts, notably Levy, who “has called for federal efforts to validate and standardize a correlate of protection.”
“Recent vaccine decisions were based on irrelevant Wuhan immunobridging,” Wiseman said. “Omicron assays are unvalidated and unverified by FDA.”
Wiseman said safety questions surrounding COVID-19 vaccines remain unanswered:
“We have shown correlations between vaccination and all-cause mortality. FDA says VAERS is under- and misreported. A FOIA disclosure reveals that CDC has not conducted safety signal analyses, which we have provided to FDA. Neurologic adverse events are finally being acknowledged [but there are] still no cancer studies.”
Wiseman further pointed out that FOIA requests show vital studies involving the spike protein have not been done:
“A Stanford study in [the journal] Cell showed vaccine message and antigen persisting for at least eight weeks. Does spike accumulate? Is this why myocarditis rates after boosting match or best primary series rates for some ages?
“Does spike persistence contribute to immune suppression, imprinting and negative efficacy? What is the toxicity of multiple doses? How will sameness of the manufacturing process be defined? Are the guidelines talking about monovalents or bivalents?”
Pfizer has dismissed concerns about the spike protein as “academic,” Wiseman said, “but it is certainly not.”
Booster formulation should be changed to combat waning efficacy, committee said
During the meeting, which occurred two weeks after the panel signed off on the primary COVID-19 vaccine series for the nation’s youngest children, a change in booster composition was deemed necessary due to waning effectiveness.
Dr. Mahesh Shenai, neurosurgeon and data analyst, said in a tweet:
“After many months of extolling benefits of vax and booster, now they are criticizing its efficacy and durability. . . to set the stage for a new updated booster!?”
In a briefing document published ahead of Tuesday’s meeting, FDA officials predicted a major COVID-19 outbreak will occur in the fall “due to the combination of waning immunity, further evolution of variants and increased indoor activity.”
A similar committee that advises the WHO recently suggested COVID-19 vaccines be reformulated to include both the original SARS-CoV-2 Wuhan variant and the first version of Omicron, BA.1 — although this variant has since been replaced by other strains of BA.4 and BA.5.
Moderna and Pfizer studied Omicron-specific vaccines in preparation for fall boosters, but efforts have been complicated by new subvariants.
If the government decides it wants a booster shot that targets BA.4 and BA.5 — two strains derived from the Omicron variant that are becoming dominant — vaccine manufacturers will have to race to produce the doses by fall, The New York Times reported.
Vaccines produced by Pfizer, Moderna, Novavax and Johnson & Johnson were developed against the original Wuhan COVID strain that emerged in 2019, but as the virus has rapidly evolved, these vaccines have become less effective.
COVID-19 vaccines target the spike protein the SARS-CoV-2 virus uses to invade human cells, but as the virus mutates away from the original strain, it has trouble “recognizing and attacking the spike,” CNBC reported. The Omicron variant has more than 30 mutations.
Marks said during the meeting he hopes changing the booster will “convince people to go get that booster,” adding the FDA plans to begin a booster campaign in October.
Megan Redshaw is a staff attorney for Children’s Health Defense and a reporter for The Defender.
© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
Doctor who sounded the alarm on jabs in ICU after plane crash
Free West Media | June 30, 2022
American doctor and vaccine critic Carrie Madej was seriously injured in a plane crash on Sunday. She is in hospital with several broken bones. Her boyfriend was also involved in the crash and has a broken back and skull. On her website there is a call to prayer.
The website SonsOfLibertyMedia.com mentioned that Madej had sent a text message on Thursday saying that she would not be giving lectures in the coming months because the medical disciplinary tribunal had been harassing her.
The US aviation authority FAA is currently investigating the crash in Meriwether County in the state of Georgia. The plane crashed at Roosevelt Memorial Airport in Warm Springs after engine problems. The doctor and her friend came down in a field north of the airport.
The small plane was en route from St. Petersburg in Florida to Newnan-Coweta County Airport. It was headed for Warm Springs. It was confirmed that Madej was in the ICU.
The doctor has been highly critical of Corona vaccines for some time. She sounded the alarm on side-effects but was censored by YouTube. “People need to know that this is not a safe vaccine,” she said. “They mess with the RNA and the DNA, the genome, the genes. That can eventually result in cancers, mutagens and autoimmune diseases.”
Madej also linked the jabs to depopulation. “Bill Gates thinks there are too many people, he wants to thin out the world population. People, wake up! This man does not want us all to stay alive. He has said it so many times in so many different ways. He is not a scientist, not a doctor, not an epidemiologist. Why are we giving him this power?”
The doctor had previously lashed out at Klaus Schwab, the founder of the World Economic Forum. Last year he said, “No one will be safe until everyone is vaccinated.” Madej shared the response to Schwab’s statement: “Over my dead body, Klaus.”
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New Book
The Garlic Book — 2026
Lies are Unbekoming | November 5, 2026
What The Garlic Book shows
The book is in four parts.
Part One, The Record, treats the history of garlic as evidence. From the clay garlic bulb placed in an Egyptian grave nearly six thousand years ago, through the Ebers Papyrus, through Hippocrates, Dioscorides, Pliny and Galen, the Arab physicians under Avicenna, the medieval herbals, Culpeper, and the plague years, to the last era in which Western physicians prescribed garlic as a matter of course, which ran from 1850 to 1945. It closes with the living traditions that never stopped using it, and with the folklore of charms, vampires and the evil eye.
Part Two, The Chemistry and the Evidence, sets out what is known about why a clove has no smell until it is cut, and why the order of crush, rest and heat changes the medicine. It then reads the clinical evidence against the historical record — bacteria, blood and vessels, cancer epidemiology, metals and fatigue — and names the trials that went against garlic as directly as the trials that went for it, including the 2007 Stanford trial funded by the US National Institutes of Health which found that raw garlic, garlic powder and aged garlic extract moved LDL cholesterol no more than placebo did. It then turns to onion, garlic’s closest relative, and reads the newer evidence published since 2015, before closing with the whole of the record through the terrain lens.
Part Three, Why Medicine Set It Aside, asks the question directly. One chapter contrasts the pharmaceutical model of isolating a single active compound with the folk model of combining whole plants, and reports what the garlic evidence says about which model works better. One chapter examines the economics of research on a plant that cannot be patented. One chapter — Fire Cider — tells the story of a folk preparation whose name was taken into a United States trademark by a Massachusetts company in 2012, and won back by three herbalists in 2014 who documented forty years of prior use through Rosemary Gladstar and her students into the older tradition.
Part Four, Garlic in Practice, is the working manual — the kitchen pharmacy, traditional uses by body system, a full chapter on safety and interactions, and a complaint-by-complaint practical guide. The book closes with The Trial That Was Never Run — a one-chapter reading of the whole evidential architecture.
At the back: two appendices (a traditional list of uses, and a preparation quick-reference), a full bibliography, and a live index.
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