Garlic has been known as a mild antibiotic for centuries — hence why vampires avoid it.
By: Daniel Y. Teng for The Epoch Times – Australia
Scientists in a “world first” study now say Australian garlic could be key to fighting COVID-19 infections and the flu.
In a study by the Melbourne-based Peter Doherty Institute, researchers extracted a specific ingredient, the Proprietary Ingredient SupaG, from Australian-grown garlic varieties.
“The results came as a world first, with the findings from specific garlic varieties proving to inhibit SARS-CoV-2 and Influenza type A viruses,” said the Victorian Chamber of Commerce in a statement.
Dr. Julie McAuley, manager of the high containment facility COVID-19 research lab at the Doherty Institute, said the team had assessed a variety of garlic products over the last 18 months—finding that a strain from Iraq was effective against COVID-19.
“We performed several blinded experiments and found one of [Australian Garlic Producers (AGP)] products could reduce the infectious titre of SARS-CoV-2 and influenza by 3-log-fold (99.9 percent). We could barely detect any remaining virus genome, indicating nearly complete virucidal activity.”
While Dr. Martin Elhay, business development director at the institute, said Doherty was committed to “the global effort to combat the spread” of COVID-19. The Doherty Institute was a prominent voice during the pandemic years on issues such as COVID-19 vaccination and public health orders.
Plans to Retail the Product
The AGP, who commissioned the study, will patent and commercialize the extraction process with plans to start retailing in supermarkets.
“Over the past 25 years, we have collected over 309 garlic cultivars from around the globe,” said Nick Diamantopoulos, CEO of the AGP.
“Our extensive R&D over many years with leading Australian universities and institutions has shown that garlic varieties not only vary in their agronomic and physiological properties but also in their biochemical properties.”
Diamantopoulos said the extensive research work is what led to the identification of “superior properties” in Australian garlic types.
The AGP harvests 100 percent of its garlic from the Australian jurisdictions of the Northern Territory, South Australia, New South Wales, and Victoria. The next study will look at the potential benefits of garlic in lowering cholesterol levels.
Paul Guerra, CEO of the Victorian Chamber of Commerce, said the partnership between the Doherty and AGP was a perfect example of how businesses and scientists could work together to deliver a “global game changer.”
Meanwhile, former federal MP Craig Kelly accused governments of spending billions on vaccines when a vegetable could have achieved the same effect.
“How stupid must the world feel today, having wasted hundreds of billions of dollars on useless vaccines and destroyed trillions of dollars of wealth with panicked lockdowns—when it’s now discovered that garlic kills COVID?” he wrote on Twitter.
“Of all the 69 reports we now have, this is the most disturbing,” expressed DailyClout CEO Dr. Naomi Wolf in a live stream on Sunday. “Because the bottom line is, according to a new tranche of Pfizer documents released just this month, this past month, April of 2023. And these are documents that go back to April of 2021 — exactly two years ago. Both Pfizer and the FDA knew that the mRNA COVID vaccine caused dire fetal and infant harms, including death.”
The batch of Pfizer clinical trial documents released in April 2023 by the Food and Drug Administration (FDA) under court order contains a shocking, eight-page document titled, “Pregnancy and Lactation Cumulative Review” …
This document is among the most horrifying yet to emerge into public view. It reveals that both Pfizer and the FDA knew by early 2021 that Pfizer’s mRNA COVID vaccine, BNT162b2, resulted in horrible damage to fetuses and babies.
• Adverse events in over 54% of cases of “maternal exposure” to the vaccine (248 out of 458). The language “maternal exposure” implies that Pfizer acknowledged intercourse, inhalation, and skin contact as methods of exposure to its mRNA injection, as also evidenced by Protocol Amendment 14.
• Six premature labor and delivery cases resulting in two newborn deaths.
• 19% (41/215) of babies in Pfizer’s records exposed to the company’s COVID mRNA vaccine via their mothers’ breast milk were recorded as suffering from 48 different categories of adverse events.
The damage and suffering feel even more real when you narrow it down to individual stories.
• “A 15-month-old infant with medical history of vomiting experienced skin exfoliation and infant irritability while being breastfed (latency <7 days). The outcome of the event’ skin exfoliation’ was not recovered and outcome of event’ infant irritability’ was unknown.”
• “A 9-month-old infant with a medical history of meningococcal vaccine and no history of allergies, asthma, eczema or anaphylaxis experienced rash and urticaria a day after exposure via lactation.”
• “A day after the mother received vaccination, a baby developed a rash after breastfeeding. At the time of the report, the event was ‘not recovered.”
• “An 8-month-old infant experienced angioedema [an area of swelling of the lower layer of skin and tissue just under the skin or mucous membranes] one day after his mother received vaccination.”
• “There were 2 cases reporting ‘illness’ after exposure via breast milk’. In the first case, a 6-month-old infant developed an unspecified sickness 2 days post-mother’s vaccination. The outcome of the event sickness was recovered, and no causality assessment was provided. The second case, a 3-month-old infant developed an unspecified illness and required hospitalization for 6 days post-exposure via breast milk (>7 days latency).”
Pfizer employee, Robert T. Maroko, approved the Review with these horrific findings on April 20, 2021.
“This is a real person working at Pfizer, Mr. Robert T. Maroko, who looked at this damage to babies, these dead babies, these dead fetuses, these miserably-injured babies — approved it and sent it on to the FDA. The FDA approved it and gave it to Rochelle Walensky and the CDC,” shared Dr. Wolf.
And three days later, on April 23, 2021, CDC Director Rochelle Walensky held a press conference, which kicked off an aggressive campaign to get pregnant women vaccinated.
“No safety concerns were observed for people vaccinated in the third trimester or safety concerns for their babies. As such, CDC recommends that pregnant people receive the COVID-19 vaccine.”
“The FDA signed off on this document showing dead babies, sick babies, dead from the injection, sick from nursing, the spontaneous abortions, or dead subsequent to the injection, the spontaneous abortions, the respiratory distress, babies hospitalized … These monsters looked at whether the babies would get sick and die or whether the fetuses would spontaneously abort, and they did. And they saw that they did, and they kept going.”
“This was just [four] months into the rollout,” Dr. Wolf mentioned. “And I want to remind you that breastfeeding has gone from 34% of moms and babies at the start of the pandemic to only 15% now, meaning that babies are having a terrible time with their mother’s breast milk. Pfizer knew they would!” she exclaimed. “Pfizer knew they would! The FDA knew they would, and they told pregnant women and lactating women to get vaccinated anyway.”
“At the end of this horrific, demonic analysis of all these sick and dying babies, all these aborted fetuses, all these babies getting sick from poisoned breast milk. Seriously sick. Damaged. They held a press conference. And Dr. Walensky, who has this report in hand, who has this report in hand,” Dr. Wolf said twice with emphasis, “told the women of America and anyone else who is listening in the world that these vaccines were safe and effective for pregnant women and for their babies. And that to protect their babies, they had to get vaccinated. They knew. They knew. Absolutely criminal.”
And there are 68 other damning reports — just like this one — using primary source Pfizer documents released under court order by the U.S. FDA.
These important summaries, which detail astonishing ranges of deaths, disabilities, and other systematic harms to subjects — damage that both Pfizer and the FDA sought to keep hidden from the public for 75 years — contain vastly important headlines: twenty forms of menstrual damage to women — how Pfizer covered up a flood of adverse events — PEG in breast milk — within a month of rollout, Pfizer knew the mRNA vaccines did not work.
Now, the information Pfizer and the FDA wanted to keep hidden for 75 years is available in paperback form. Funds and proceeds raised go to the research project, which helps makes more Pfizer Documents Analysis Reports possible. So, please, show your support and get your hands on this critical information in one place — by ordering your copy today.
The old vaxes haven't killed/injured a high enough percentage of the people.
Story by Karen Weintraub, USA TODAY
Bracketed comments by Phoenix
The Biden Administration Monday announced a $5 billion program to accelerate the development of next-generation COVID-19 vaccines and treatments.
[Of course, the elephant in the room is: “Why? We already have effective treatments, ones that don’t kill people.” Oh, wait: they’re cheap, and Big Pharma can’t make more Billion$ from them. Carry on…..]
Like Operation Warp Speed, which developed and distributed vaccines in the early days of the pandemic, Project NextGen will cut across government agencies and involve public-private collaborations, a senior Biden official told USA TODAY.
Current vaccines, developed rapidly in the heat of the emergency, are “really good, but they’re not great,” said Michael Osterholm, an epidemiologist who worked with the administration to develop the new program. “There is a substantial amount of work (to be done) to take these good vaccines and hopefully achieve better vaccines.”
Project NextGen has three primary goals, which Osterholm and colleagues laid out in a “roadmap” issued in February: Develop a nasal vaccine that will hopefully prevent infection as well as severe disease; develop longer-lasting vaccines; and create “broader” vaccines that protect against all variants and several different coronaviruses
[ Why do they need a “new” nasal vax when two already exist? Oh, wait. Same answer.]
It will also include funding to develop more durable monoclonal antibodies resistant to new variants, according to the administration. Antibodies were highly effective treatments earlier in the pandemic but have not been able to keep up with the virus as it evolved and are no longer available.
The Biden administration Monday announced a $5 billion program to accelerate the development of next-generation COVID-19 vaccines and treatments.
Like Operation Warp Speed, which developed and distributed vaccines in the early days of the pandemic, Project NextGen will cut across government agencies and involve public-private collaborations, a senior Biden official told USA TODAY.
Current vaccines, developed rapidly in the heat of the emergency, are “really good, but they’re not great,” said Michael Osterholm, an epidemiologist who worked with the administration to develop the new program. “There is a substantial amount of work (to be done) to take these good vaccines and hopefully achieve better vaccines.”
Project NextGen has three primary goals, which Osterholm and colleagues laid out in a “roadmap” issued in February: Develop a nasal vaccine that will hopefully prevent infection as well as severe disease; develop longer-lasting vaccines; and create “broader” vaccines that protect against all variants and several different coronaviruses
It will also include funding to develop more durable monoclonal antibodies resistant to new variants, according to the administration. Antibodies were highly effective treatments earlier in the pandemic but have not been able to keep up with the virus as it evolved and are no longer available.
The administration said the initial allocation of $5 billion for Project NextGen would be financed through money saved from contracts costing less than originally estimated. The investment was first reported Monday by the Washington Post.
Dr. Gregory Poland, director of the Mayo Clinic’s Vaccine Research Group who was also involved in the earlier roadmap, said he and others have been advising the White House since last summer to launch something like Project NextGen.
The funding is a start, he said, “but much more will be needed to accomplish all three goals,” he said. “The need though is urgent and now – something government generally doesn’t do well, hence the key will be prioritization and implementation.”
The Biden administration Monday announced a $5 billion program to accelerate the development of next-generation COVID-19 vaccines and treatments.
Like Operation Warp Speed, which developed and distributed vaccines in the early days of the pandemic, Project NextGen will cut across government agencies and involve public-private collaborations, a senior Biden official told USA TODAY.
Current vaccines, developed rapidly in the heat of the emergency, are “really good, but they’re not great,” said Michael Osterholm, an epidemiologist who worked with the administration to develop the new program. “There is a substantial amount of work (to be done) to take these good vaccines and hopefully achieve better vaccines.”
Project NextGen has three primary goals, which Osterholm and colleagues laid out in a “roadmap” issued in February: Develop a nasal vaccine that will hopefully prevent infection as well as severe disease; develop longer-lasting vaccines; and create “broader” vaccines that protect against all variants and several different coronaviruses
It will also include funding to develop more durable monoclonal antibodies resistant to new variants, according to the administration. Antibodies were highly effective treatments earlier in the pandemic but have not been able to keep up with the virus as it evolved and are no longer available.
The administration said the initial allocation of $5 billion for Project NextGen will be financed through money saved from contracts costing less than originally estimated. The investment was first reported Monday by the Washington Post.
Dr. Gregory Poland, director of the Mayo Clinic’s Vaccine Research Group who was also involved in the earlier roadmap, said he and others have been advising the White House since last summer to launch something like Project NextGen.
The funding is a start he said, “but much more will be needed to accomplish all three goals,” he said. “The need though is urgent and now – something government generally doesn’t do well, hence the key will be prioritization and implementation.”
Why do we need new coronavirus vaccines?
When the current vaccines were developed, speed was a priority along with safety and effectiveness. They were 95% effective at preventing all disease when first released in late 2020. But their effectiveness against mild disease, in particular, wanes over just a handful of months.
Protection may also not be as good as the virus continues to evolve. The current bivalent booster is aimed at both the original virus and the BA.5 variant.
But SARS-CoV-2, the virus that causes COVID, is the third new coronavirus to pop up in the last two decades, following Middle-Eastern Respiratory Syndrome (MERS) and Severe Acute Respiratory (SARS). If and when a fourth turns up, it would be great to already have a vaccine that could protect against” it,’ said Osterholm, who directs the Center for Infectious Disease Research and Policy at the University of Minnesota.
[ “…when a fourth turns up, it would be great TO ALREADY HAVE a vaccine that could protect against it…” Hmm, Bill Gates & friends have already told us there’s another pandemic coming, is there something they know that we don’t?]
A nasal vaccine is the third item on the wish list. The idea is that by delivering a vaccine directly to the area where the virus enters the body, scientists could set up a barrier of protection to prevent even mild infections and transmission from one person to the next.
[But didn’t they tell us initially that surface contact would spread it? DISINFECT EVERYTHING! And what about people who breathe more through their mouths — like people with allergies such as Hay Fever?]
“I think an initiative like this is much needed and should have been put in place much sooner,” said John Moore, an immunologist at Weill Cornell Medical College in New York.
What happens next?
Reaching these goals will likely be more difficult than it sounds, Moore said.
“Anyone familiar with vaccine development knows that translation into a practical product is a much harder and more expensive process” than simply creating a basic vaccine, he said. “A lot of designs that look good in the early stages fizzle out because they cannot be manufactured efficiently under the conditions required for human trials.”
[And when did they have time for human testing under Warp Speed?]
Dr. Paul Offit, a pediatrician who directs the Vaccine Education Center at Children’s Hospital of Philadelphia, is skeptical that any of these goals are realistic.
Researchers have been trying for more than 40 years to develop vaccines against multiple strains of flu and against HIV, the virus that causes AIDS. Both have proven elusive, he said, because the viruses mutate so much, as does SARS-CoV-2.
Meanwhile, nasal vaccines are still being tested in clinical trials, so it’s not yet clear how effective they’ll be against COVID. A nasal vaccine for the flu doesn’t provide any more protection than a shot, Offit said, and it’s most effective in young children who have never been exposed to the flu virus before. At this point, nearly every American has already been exposed to the virus that causes COVID.
Moore agrees that developing a nasal vaccine should be a high priority, but “it’s seriously naive to believe that it will be easy to make one.”
Offit worries that the emphasis on making COVID vaccines better will undermine public trust in the ones we already have. He said the current vaccines have been “amazing,” but that vaccines can only do so much.
What did Operation Warp Speed do?
Under the Trump administration, Operation Warp Speed spent about $30 billion beginning in March 2020 to develop, manufacture and distribute COVID-19 vaccines.
The federal government essentially placed bets on six different drug companies hoping at least a few of them would prove successful. Each received over $1 billion (although Pfizer/BioNTech developed its vaccine without government support) with a promise of a guaranteed market if they succeeded.
►Moderna and Pfizer/BioNTech both developed, tested, passed regulatory hurdles and produced millions of doses of their mRNA vaccines in under a year. Previously, the fastest vaccine had taken four years to bring to market.
►Johnson and Johnson also developed a vaccine based on a different technology. While effective, the vaccine led to a rare side effect and is no longer widely available in the United States.
►Novavax pursued a third type of vaccine technology and has also won emergency regulatory approval, though it is not widely available.
►The other two efforts, one by Sanofi and another by AstraZeneca, fell behind early and were not advanced beyond preliminary testing.
[It’s obvious I’m skeptical of the claims here. If the previous record for developing a vaccine was FOUR YEARS, how did they manage to develop –AND TEST– them so quickly (less than a third of that time)? Why weren’t these vaccines pulled after the deadly side effects became apparent? It only took a ‘mere’ 50 deaths to yank the swine flu vaccine; how many THOUSANDS have died/been seriously affected by the clot shots?]
Dr Rappuoli was the head of vaccine research and development at GSK, the Big Pharma behemoth formerly known as GlaxoSmithKline. Which had to pay a $3 BILLION fine for health care fraud. Hmm.
The longtime government bureaucrat links up with infamous Big Pharma heavyweights for a new consultant gig.
In news that has somehow remained entirely unreported in the United States, Dr Anthony Fauci seems to have inked his first gig outside of U.S. Government Health, where he is reportedly still taking a salary.
According to several Italian press reports, Fauci has agreed to serve in a consulting capacity to a newly created “anti-pandemic” bio lab, which is being run by a high-level Italian scientist and longtime pharmaceutical executive.
“American immunologist Anthony Fauci has agreed to act in an informal capacity as a strategic advisor to Rino Rappuoli, scientific director of the Biotecnopolo biotech hub in Siena, an institution founded by the Ministries of the University, Health, Economy and Industry with the aim of focusing on applied research in biotechnologies and life sciences, the Fondazione Biotecnopolo announced this week.”
The news was also reported by Italy’s L’Eco di Bergamo and others, but there seem to be no reports on the matter outside of the country.
Biotecnopolo, the newfound bio lab that is funded by the Italian government, is self-described as “an anti-pandemic hub with a particular focus on the development and production of vaccines and monoclonal antibodies for the treatment of emerging epidemic-pandemic pathologies.”
Rome has already committed hundreds of millions of Euros to the noticeably below-the-radar state-backed project.
What is an “Anti Pandemic Center?”
In a press release, a board member declared that Fauci’s new role will be “a fundamental step towards making the Biotecnopolo the Italian hub for the research, study and prevention of pandemics”.
Fauci has not released a statement on the matter. Dr Rappuoli did not reply to a request for comment.
It still remains unclear why Fauci, a lifelong American government bureaucrat, has decided to become a consultant for an entity funded by the Italian government. On several occasions, he has spoken highly about his Italian heritage. In 2020, the Italian government awarded him with the Order of Merit of the Italian Republic.
Italy and the United States share a lot when it comes to the humanitarian catastrophes our governments imposed in the name of a virus. Dr. Fauci, campaigned for coronavirus lockdowns that modeled after Italy’s response. What remained unspoken was that Italy got the idea for its brutal lockdowns from China. Both Fauci and Dr Deborah Birx, his longtime mentee, remained committed to the Italian model for several years, declaring Italy as the gold standard for “the measures.”
Moreover, Fauci’s new “informal” relationship with Dr Rappuoli should raise some eyebrows.
Before becoming the chief scientist for the new bio lab, Dr Rappuoli was the head of vaccine research and development at GSK, the Big Pharma behemoth formerly known as GlaxoSmithKline. He is also the Professor of Vaccines Research at Imperial College, London, the home of the infamous computer model simulations that helped to launch the coronavirus hysteria.
GSK is known for record setting fraudulent activity. In 2012, GSK agreed to pay a $3 billion settlement to the U.S. government, breaking Pfizer’s record for the largest health-care fraud settlement for a drugmaker in U.S. history.
Last year, Fauci spoke at a conference organized by GSK on the “role of vaccines in protecting people and the planet.”
So Fauci has now linked up with Big Pharma heavyweights and he’s an advisor for a clandestine bio lab project being financed by the Italian government. What could possibly go wrong?
After receiving Pfizer’s Respiratory Syncytial Virus (RSV) shot during a clinical trial, two older individuals contracted Guillain-Barré syndrome.
People around the globe have suffered serious adverse reactions resulting from COVID vaccines, especially from the Pfizer shot.
Now the Food and Drug Administration (FDA) tells us another Pfizer vaccine can cause serious complications in recipients. After receiving Pfizer’s Respiratory Syncytial Virus (RSV) shot during a clinical trial, two older individuals contracted Guillain-Barré syndrome.
This was enough for the FDA to flag the disease as “an important potential risk” from the RSV shot. Yet Pfizer is still seeking approval for general public use.
According to the Mayo Clinic, Guillain-Barré syndrome is a rare disorder in which your body’s immune system attacks your nerves.
While most people recover from Guillain-Barre syndrome, some severe cases can be fatal. Other serious cases can result in paralysis.
There’s no known cure for Guillain-Barre syndrome.
The Gateway Pundit previously reported on individuals contracting the disorder after receiving the COVID vaccine. One person became partially paralyzed from the waist down and suffered full facial paralysis from the disease shortly after he was vaccinated.
The Food and Drug Administration (FDA) stated that two older adults who received Pfizer’s respiratory syncytial virus (RSV) vaccine during a clinical trial were subsequently diagnosed with the rare neurological disorder Guillain-Barré syndrome.
Briefing documents released on Feb. 24 ahead of this week’s meeting of the Vaccines and Related Biological Products Advisory Committee flagged the two cases of the disorder and stated that Pfizer’s vaccine poses a potential risk.
“Given the temporal association and biological plausibility, FDA agrees with the assessments of the investigators that these events were possibly related to study vaccine,” the FDA stated in the documents. “Therefore, [Guillain-Barré] is being considered an important potential risk.”
Two people in their 60s who received the RSV vaccine were diagnosed with Guillain-Barré syndrome in a phase 3 trial, which involved 20,000 recipients of the vaccine. There were no instances of the neurological disorder in people who received a placebo.
The briefing documents show that the FDA asked Pfizer to conduct a safety study if the RSV vaccine is approved in the spring.
No safety concerns were identified by Pfizer during the trial and the company stated that it would carry out a safety study on its RSV vaccine if approved.
The FDA’s briefing documents state that Pfizer’s RSV vaccine was 85.7 percent effective at preventing severe illness.
Only a naïve individual would believe Pfizer’s claims regarding effectiveness after what they said about their COVID vaccine. One should also count on more complications arising from “unknown” causes should the FDA approve Pfizer’s RSV shot.
Side effects include a multitude of things the shot should NOT be doing.
That means that over 40 million women in the United States have had their menstrual cycles affected by the C19 jab.
Project Veritas released another breaking story last night (Feb. 2) featuring Pfizer executive Jordan Trishton Walker. This time, he was caught on camera openly admitting concern about women’s cycles and their fertility. As a result, #Pfertility is trending on Twitter.
In light of Project Veritas’ latest bombshell, we have compiled an array of respected voices speaking out about menstrual and fertility concerns. Doctors, scientists, thought leaders, and women across the globe have been screaming from the rooftops on this subject for years now.
(In the interest of brevity, I’ll just post the videos from Vigalent Fox [there are quite a few]. The full article, with Twitter comments, can be found HERE , Some may be out of order —TPR)
Basically, Pfizer knew that there would be problems, they knew that lipid nanoparticles such as in the clot shot accumulated in the ovaries, and Bill Gates (bless his heart) was studying ways to interfere with reproduction.
Although the pandemic is behind us, Big Tech is still censoring health information from the public.
The video hosting company Vimeo recently deleted the channel of The Wellness Company.
The Wellness Company is a startup with a “Freedom From Pharma” program that provides access to doctors and pharmacies that aren’t afraid to provide treatments like ivermectin and hydroxychloroquine (plus, Gateway Pundit benefits when you subscribe through this link or the links below).
In fact, it was a video on ivermectin that caused the deletion, according to The Wellness Company.
Chris Alexander of The Wellness Company said:
“Vimeo banned our account on the basis of an interview with Jen VanDeWater, a licensed pharmacist who runs our Freedom from Pharma program, about the safety and utility of Ivermectin.
“Vimeo has allowed pro-vaccination voices to post video after video that have been riddled with misinformation, disinformation and outright lies. Vimeo isn’t holding any of these people accountable and none of these accounts are being suspended or permanently banned.
“The actions of Vimeo are a reminder of why it is so important for conservatives and freedom loving Americans to build parallel systems. We can no longer rely on the compromised systems of the establishment – and that is exactly why we founded The Wellness Company.
“Nothing is more critical than healthcare and no system has been more exposed over the last three years than our healthcare system. Every American who cares about the truth and who cares about their health should join us!”
By Zachary Stieber for Epoch Times January 9, 2023Updated: January 10, 2023
A Pfizer board member who used to head the U.S. Food and Drug Administration (FDA) lobbied Twitter to take action against a post accurately pointing out that natural immunity is superior to COVID-19 vaccination, according to an email released on Jan. 9.
Dr. Scott Gottlieb wrote on Aug. 27, 2021, to Twitter executive Todd O’Boyle to request Twitter take action against a post from Dr. Brett Giroir, another former FDA commissioner.
“This is the kind of stuff that’s corrosive. Here he draws a sweeping conclusion off a single retrospective study in Israel that hasn’t been peer reviewed. But this tweet will end up going viral and driving news coverage,” Gottlieb wrote.
Giroir had written that it was clear natural immunity, or post-infection immunity, “is superior to vaccine immunity, by ALOT.” He said there was no scientific justification to require proof of COVID-19 vaccination if a person had natural immunity. “If no previous infection? Get vaccinated!” he also wrote.
Giroir pointed to what was at the time a preprint study from Israeli researchers that found, after analyzing health records, that natural immunity provided better protection than vaccination. The study was later published in the journal Clinical Infectious Diseases following peer review.
Researchers said the data “demonstrated that natural immunity confers longer lasting and stronger protection against infection, symptomatic disease and hospitalization caused by the Delta variant of SARS-CoV-2, compared to the BNT162b2 two-dose vaccine-induced immunity.” BNT162b2 is the trade name for Pfizer’s COVID-19 vaccine, which is the main shot used in Israel.
Gottlieb’s email triggered messages on Jira, Twitter’s internal messaging system, according to journalist Alex Berenson, who was granted access to Twitter’s internal files by CEO Elon Musk.
“Please see this report from the former FDA commissioner,” O’Boyle wrote.
A Twitter analyst who reviewed the post determined it did not violate any misinformation rules but Twitter still put a tag on it, claiming to all users who viewed it that it was “misleading” and directing them to a link that would show “why health officials recommend a vaccine for most people.” The tag prevented people from replying to, sharing, or liking Giroir’s post.
Gottlieb later defended his actions, saying he targeted posts that he thought included “false and inflammatory” information. Giroir said “my tweet was accurate then, and it remains so now” and that Twitter never responded to him.
Another Message
Gottlieb later messaged O’Boyle again, flagging a post from Justin Hart, a critic of lockdowns and a skeptic of COVID-19 vaccines, Berenson reported.
Gottlieb took issue with Hart writing that “sticks and stones may break my bones but a viral pathogen with a child mortality rate of <>0% has cost our children nearly three years of schooling.”
COVID-19 poses little mortality risk to young, healthy people, studies and data show.
Gottlieb did not detail why he wanted to censor Hart, but the objection came shortly before the U.S. government authorized and recommended Pfizer’s vaccine for children aged 5 to 11.
O’Boyle sent the request to Twitter analysts, failing for a second time to disclose Gottlieb’s ties to Pfizer. The complaint did not trigger any action.
“Our team of ragtag analysts, activists, moms and dads have been going after Scott since April 2020 when he repeatedly advocated for school closures and lockdowns. He doesn’t like people pushing back on the narrative,” Hart told The Epoch Times in a Twitter message.
Twitter did not respond to requests for comment.
Tried to Get Journalist Banned
Gottlieb also tried to get Berenson, a former New York Times reporter who now authors a Substack, banned from Twitter, a message released in 2022 showed.
The message showed that Gottlieb forwarded a blog post from Berenson to a Twitter worker, writing that Berenson calling Dr. Anthony Fauci arrogant was an example of why Fauci, at the time the head of the U.S. National Institute of Allergy and Infectious Diseases, needed a security detail.
Four days later, and a day after Gottlieb met with Twitter workers, Twitter banned Berenson for allegedly violating its rules on COVID-19 misinformation.
Gottlieb defended his actions.
“I’ve raised concerns around social media broadly,” Gottlieb said during an appearance on CNBC. “And I’ve done it around the threats that are being made on these platforms, and the inability of these platforms to police direct threats, physical threats about people, that’s my concerns around social media, and what’s going on in that ecosystem.”
“I am very concerned with physical threats being made against people’s safety and the people who gin up those threats against individuals,” he also said.
Berenson responded that he’d never threatened Fauci or Gottlieb and referred to Gottlieb’s comments.
In the post that triggered Gottlieb’s email, Berenson criticized Fauci for saying that “attacks on me are attacks on science” and how he handled the U.S. pandemic response.
Berenson was reinstated to Twitter in 2022 as part of a settlement of a lawsuit he brought against the company. Berenson obtained Gottlieb’s email about Fauci’s post during discovery. Before the settlement agreement, a judge had concluded that Berenson plausibly alleged Twitter failed to abide by a policy of five strikes before banning the journalist.
Reaction on ET:
Jack−
Thousands of people LOST THEIR JOBS or were coerced into getting the jab after they’d recovered from CV19 because of people like Gottlieb trying to keep the truth about natural immunity from reaching mainstream news. Some of those people who were coerced into getting it subsequently had debilitating effects from the job, in some cases lifelong or even life-ending, again because of people like Gottlieb. I have had people bar me from their homes and literally shrink away from me when they heard that I, a completely healthy person who was far safer to be around than those who had been vaccinated, hadn’t received the shot. Again, because of Gottlieb. People like him literally are creating hell on earth by their ambitions. And there are still a lot of people out there to this day, particularly some of the elderly or people that only get their news from one source, that remain shrouded in ignorance, that don’t realize their fear of the unvaccinated is based on lies. But they still fear and shun those with natural immunity.
Ear infection concept. an inflammatory disease of the middle ear.
The hits just keep coming from these shots – is this the new definition of “safe and effective?”
By Dr. Peter A. McCullough Dec 20, 2022
Loss of hearing in the elderly is common affecting both the patient and the people around them trying to communicate.
I have noticed many of my vaccinated elderly patients developing progressive hearing loss. Nieminen et al have conducted an extensive hearing assessment of patients in Finland after COVID-19 vaccination and compared them to the unvaccinated. The data suggested each successive shot increased risk for hearing loss. However, the most important results are in the supplemental tables which demonstrate the elderly and those with risk factors for hearing loss are pushed over the edge by COVID-19 vaccination.
Nieminen TA, Kivekäs I, Artama M, Nohynek H, Kujansivu J, Hovi P. Sudden Hearing Loss Following Vaccination Against COVID-19. JAMA Otolaryngol Head Neck Surg. Published online December 15, 2022. doi:10.1001/jamaoto.2022.4154
Their risk for sudden and substantial loss of hearing is more than double those who wisely deferred on the vaccines.
The Spike protein produced by the vaccines is a neurotoxin damaging nerves throughout the body and likely having more of an impact in nervous tissue which is already degenerated such as the auditory nerve. It is also possible the Spike protein incites inflammation leading to fibrosis in the tissue holding the stapes or stirrup which is a bone in the middle ear, the annular ligament, or the oval window all involved in the conduction of sound vibrations to the inner ear.
If you have an elderly person in your circle who has been vaccinated, check on their hearing and do not fall behind on progressive hearing loss which if unchecked, can lead to social withdrawal and insidious depression.
By: The Vigilant Fox (a citizen journalist with 12 years of healthcare experience, focused on The Great Reset, world protests, and COVID-19.) December 21, 2022
Something strange is going on with the VAERS system. Reports that were present three months ago are now inexplicably missing. And fewer than 4% of adverse events recorded in V-Safe have made their way to VAERS. This is the CDC’s database; Rochelle Walensky is in charge of it. And their failure to properly manage VAERS is suppressing the already-alarming safety signal of the Covid-19 shots.
Fifty deaths pulled the swine flu vaxx off the market. Covid-19 vaxxes caused FIFTY deaths by January 2021!
Now, what is VAERS? VAERS stands for Vaccine Adverse Event Reporting System. As mentioned earlier, VAERS is a database put in place in 1990 under the supervision of the CDC. Reports of suspected vaccine adverse events take about half an hour to fill out, and 86% of the time, this is done by a doctor, nurse, paramedic, coroner, or healthcare professional in which he or she believes the adverse event is related to a vaccine reaction. And because of its lengthy report process as well as the lack of awareness of the existence of VAERS, there is a general consensus of a severe underreporting factor for this database.
To get a better idea of what’s going on with the CDC’s handling of the VAERS system, Dr. Naomi Wolf spoke with Dr. Henry Ealy, an expert on the database.
Dr. Henry Ealy is the Founder & Executive Community Director for the Energetic Health Institute. He holds a Doctorate in naturopathic medicine and has been at the tip of the spear on the Grand Jury front — taking action to bring forth a Grand Jury investigation of the CDC for allegations of criminal data fraud and willful misconduct.
“You mentioned that V-Safe should be added to VAERS, but only 4% of V-Safe [adverse events have been] added. Can you explain what that means to people and why it matters?” asked Dr. Wolf.
Dr. Ealy explained, “VAERS is designed specifically for medical professionals and people alike to report, ‘Hey, I got hurt.’ And when enough people have gotten hurt for officials to look at it and say, ‘Hey, this product isn’t safe; it’s got to come off the market.’ V-Safe was created (by the CDC) to also do something similar to that — and to make that process a little bit easier. You don’t need as much information to record a report in V-Safe.”
By streamlining the process, the CDC got inundated with adverse event reports from the Covid-19 shot. Out of the 10,108,273 individual users, 800,000 had an adverse event — or about 1 in 13. And of those 800,000 V-Safe reports, only 30,492 have been logged into VAERS.
Dr. Ealy continues, “In V-safe, there have been over 800,000 reports of injury. And the deal was that in V-Safe, every single report of injury was supposed to also then subsequently have a VAERS report associated with it. So that means all 800,000 should be in VAERS. But unfortunately, or by design — however you want to look at it — only just over 30,000 of those 800,000 have been recorded in VAERS. So what that means is that fewer than 4% of the records in V-Safe have actually been reported in VAERS as they were supposed to be done.”
“What a sneaky way to basically sweep almost 800,000 adverse events under the rug,” remarked Dr. Wolf.
To add insult to injury, not only are the bulk of V-Safe reports not making their way to VAERS, but Dr. Ealy suspects that VAERS reports are being removed.
What were 45,388 reports three months ago has now inexplicably dropped down to 12,544.
Specifically, he notes that between September 2022 and December 2022, the CDC has removed at least 32,844 records of injury related to the following conditions: myocarditis, pericarditis, and heart inflammation. What were 45,388 reports three months ago has now inexplicably dropped down to 12,544.
Note the different totals between first chart and this one
Dr. Ealy stresses he’s “triple-checked this,” and he stands by the allegation that they are removing or obfuscating records.
Dr. Jessica Rose has also reported similar issues with VAERS. She wrote on November 19, “The foreign data set was gutted this week in VAERS, and the cancer signal was halved. The myocarditis dose three response signal was lost, and 994 spontaneous abortions/stillbirths were dropped.”
So, from two credible sources, it is appears that the CDC is removing records.
“It’s not an accident they would do this,” attested Dr. Ealy. “With Dr. Ladapo and Governor DeSantis coming out with that study about myocarditis and pericarditis, they’re trying to do everything they can to delete records to thwart what Governor DeSantis and (Florida) Surgeon General Dr. Ladipo are doing.”
“I’m stunned,” expressed Dr. Wolf. “This is as big as the Pentagon Papers, easily, if indeed the CDC deleted those records. I’ve seen the screenshots; it looks pretty bad. And so, you’re saying that Dr. Ladapo and Governor DeSantis calling for a Grand Jury investigation could be the reason that they’re deleting these, basically, evidence of their crimes? Because Ladapo and DeSantis will be investigating that data? Is that what you’re saying?”
“Right,” confirmed Dr. Ealy. “When you read through the Grand Jury petition that Governor DeSantis signed and submitted to the Florida Supreme Court, they are putting a lot of what their argument based upon their findings with myocarditis. So myocarditis and pericarditis — and that’s not without good reason.”
Dr. Ealy continues, “So the issue is — if you’re the CDC now — and you know you’ve been complicit in data fraud from day one, what do you start doing? Well, you’ve been deleting records for the last couple of years. Why not delete the records specific for myocarditis and pericarditis to try to thwart their attempts and try to discredit their analysis of what they’re doing? That’s what it looks like to me right now.”
“That’s many felonies!” exclaimed Dr. Wolf. “That’s not just a felony in terms of data handling — that’s a felony in terms of the criminal process, right? Isn’t that covering up evidence of a crime?
“Well, yeah. It would definitely [be],” replied Dr. Ealy.
The problem with VAERS as a federal system is yes, maybe if there is an erroneous record here or there, you should have the ability to delete it. But when you started seeing the CDC deleting hundreds of thousands of records and removing, in this case, over 32,000 records, or at least removing the search term. That’s my suspicion here — that they didn’t delete the record. What they deleted was that word — ‘myocarditis’ or ‘pericarditis or ‘heart inflammation’ in the actual report. And so, that’s modification of official records. And when you do that, that’s now criminal fraud — again. And, of course, it throws off our ability to really understand what’s going on with this because we rely on systems like this to give us information for making decisions.”
Dr. Wolf argues the CDC’s actions appear to be a “cover-up of evidence of mass murder.”
And she pleas Governor DeSantis and Surgeon General Ladapo to get in touch with Dr. Ealy’s team “because what you all have uncovered is absolutely stunning.” “And this latest, which you’ve presented, should be on the cover of every newspaper and every magazine and every news site in the world. This is huge if, indeed, they’re concealing myocarditis outcomes.”
