Worked in 2020 will it work in 2024? China sending another medical threat? Tony the Fauch ready to come out of retirement? Yes my friends it looks as it China is at it again. Don’t believe me? just ask the WHO. We have this from NBC.
World Health Organization (WHO) announced that it has requested information from China regarding the increase in cases of respiratory diseases and clusters of pneumonia among children.
But China said not to worry there’s nothing here so go on and leave us alone. Of course the WHO went along with China and said no travel restrictions against our friend China.
Chinese authorities attributed the increase in respiratory disease cases to the end of restrictions imposed to contain COVID-19 and the circulation of known pathogens. You buying that?
Barack Obama shakes hands with Francis Collins, director of National Institutes of Health, in 2009. Collins said warnings of dangerous genetically engineered viruses were ‘science fiction’ In the last days of the administration, he said at a contentious WH meeting that a DOE threat assessment “reads like a movie script.”
“Delete That Comment”
In late October 2017, a US health official from the National Institute of Allergy and Infectious Diseases (NIAID) arrived at the Wuhan Institute of Virology for a glimpse of an eagerly anticipated work in progress. The WIV, a leading research institute, was putting the finishing touches on China’s first biosafety level 4 (BSL-4) laboratory. Operating with the highest safeguards, the lab would enable scientists to study some of the world’s most lethal pathogens.
The project had support from Western governments seeking a more robust partnership with China’s top scientists. France had helped design the facility. Canada, before long, would send virus samples. And in the US, NIAID was channeling grant dollars through an American organization called EcoHealth Alliance, a controversial research group at the center of the Covid lab leak theory, to help fund the WIV’s cutting-edge coronavirus research.
That funding allowed the NIAID official, who worked out of the US embassy in Beijing, to become one of the first Americans to tour the lab. Her goal was to facilitate cooperation between American and Chinese scientists. Nevertheless, says Asha M. George, executive director of the Bipartisan Commission on Biodefense, a nonprofit that advises the US government on biodefense policy, “If you want to know what’s going on in a closed country, one of the things the US has done is give them grant money.”
The lab — where theFBI believes Covid leaked from — was found to have a ‘serious shortage of appropriately trained technicians and investigators needed to safely operate’.
The official — who is unnamed due to concerns for her safety — from the NIAID, run by Anthony Fauci at the time, was instructed to erase the safety failures in her report to avoid angering China.
And this wasn’t the first time concerns over engineered viruses were dismissed. A year prior, US officials at the DOE warned the NIAID of the dangers of genetically engineered and altered pathogens. However, longtime head of the NIH, Francis Collins, called the claims ‘science fiction.’
The NIAID official told her superiors what she’d gleaned from the technician who’d served as her guide. The lab, which was not yet fully operational, was struggling to develop enough expertise among its staff—a concern in a setting that had no tolerance for errors. “According to [the technician], being the first P4 [or BSL-4] lab in the country, they have to learn everything from zero,” she wrote. “They rely on those scientists who have worked in P4 labs outside China to train the other scientists how to operate.”
She’d also learned something else “alarming” from the technician, she wrote. Researchers at the WIV intended to study Ebola, but Chinese government restrictions prevented them from importing samples. As a result, they were considering using a technique called reverse genetics to engineer Ebola in the lab.
Anticipating that this information would set off alarm bells in the US, the official cautioned, “I was shocked to hear what he said [about reverse engineering Ebola]. I also worry the reaction of people in Washington when they read this. I don’t want the information particularly using reverse genetics to create viruses to get out, which would affect the ability for our future information gain,” meaning it would impair the collaboration between NIAID and the WIV. “I don’t feel comfortable for the broader audience within the government circle [to hear this]. It could be very sensitive.”
There was good reason to fear that such a revelation could derail the fledgling partnership. One year earlier, the US Department of Energy had warned other agencies, including NIAID’s parent entity, the National Institutes of Health (NIH), that advanced genetic engineering techniques could be misused for malign ends. The Energy Department had developed a classified proposal, reported on here for the first time, to ramp up safeguards against that possibility and develop tools to better detect evidence of genetic engineering. The proposal, which was not implemented in its suggested form, prompted a heated interagency battle.
F. Gray Handley, then NIAID’s associate director for international research affairs, responded to the email agreeing with the official. His response included: “As we discussed. Delete that comment.”
On January 19, 2018, the US embassy in Beijing issued a sensitive but unclassified cable that included details from the NIAID official’s tour. It said that WIV scientists themselves had noted the “serious shortage of appropriately trained technicians and investigators needed to safely operate” the lab, according to an unredacted copy obtained by Vanity Fair. But the cable did not include the information that her NIAID colleagues apparently found most worrying.
For synthetic biologists, the idea of engineering Ebola isn’t seen as particularly unusual. Reverse genetics, using the CRISPR gene editing technology developed roughly a decade ago, is now a widely used laboratory technique. The WIV’s BSL-4 laboratory was designed to safely research Ebola, be it natural or man-made. Some scientists argue that, for research purposes, it can be safer to make a deadly pathogen in-house than to risk transporting it.
However, according to Stanford microbiologist David Relman, the risks of the WIV producing something new or unknown may have driven the government’s concern. “When you are reverse engineering Ebola, you have now established a platform from which you can do [a] million different things with Ebola, or something that you call Ebola,” he says. “It means you can now make any variant or construct that is Ebola-like at will.”
US government warnings about scientific collaborations in autocratic countries predate the pandemic and cut across partisan lines.
Any effort to shield the technician’s Ebola remarks from wider scrutiny within the federal government would be “a dereliction of responsibility,” says Gerald Parker, former commander of the US Army Medical Research Institute of Infectious Diseases (USAMRIID).
Some view ongoing questions about biosafety at the WIV as part of a Republican campaign to discredit Anthony Fauci, who led NIAID for 38 years. But US government warnings about scientific collaborations in autocratic countries predate the pandemic and cut across partisan lines. Concerns flagged in the Obama administration persisted through the Trump administration and are being examined today.
“There’s a dark side” to certain research, says Jason Paragas. “Just because you’re doing it to publish a paper doesn’t mean no one is going to do anything bad.”
Between 2015 and 2023, at least seven US entities supplied NIH grant money to labs in China performing animal experiments, totaling $3,306,061 — that we know about.
“Serious Security Concerns”
Operating out of a sprawling 300-acre campus in Bethesda, Maryland, the National Institutes of Health describes itself as “the federal focal point for health research.” Each year it makes more than 50,000 grants, distributing the majority of its $48 billion budget to researchers in the US and around the world. Among its 27 institutes and centers is NIAID, which distributed $5.3 billion in the 2023 fiscal year alone.
For the NIH and its grantees, global collaboration and transparent data sharing are synonymous with scientific progress. Even a trickle of grant money to a foreign lab can pay dividends. It can give US researchers access to new environments and viruses and help build trust that may elude bickering governments. “It is almost always beneficial to exchange ideas and samples with other countries, particularly those with different climates than our own,” says Marc Lipsitch, a professor of epidemiology at the Harvard T.H. Chan School of Public Health. “I don’t see why science funding should be reserved for friendly countries.”
But within the federal government, there is a different world of scientists: those tasked with anticipating threats to national security. In the open exchange of cutting-edge research with scientists in autocratic countries, they see the risk that science that serves the public good could be misappropriated to cause harm—a phenomenon known as dual-use research of concern. Worries about dual-use research have only grown with the easy accessibility of DNA-editing tools. Those technologies have opened the door to miraculous treatments, such as using gene editing to reduce cholesterol and protect against heart disease. But “there’s a dark side” to certain research, says Jason Paragas, former director of innovation at the Lawrence Livermore National Laboratory in California. “Just because you’re doing it to publish a paper doesn’t mean no one is going to do anything bad.”
Lawrence Livermore is one of 17 national laboratories overseen by the Department of Energy, a science and technology agency with strong intelligence capabilities, a number of whose scientists regularly review classified threats. “They spend their time in a dark world, faced with the nastiness of what could go on,” says Diane DiEuliis, a distinguished research fellow at the National Defense University. Sometimes they flag concerns for scientists who, given their focus on open research, are “not willing to even contemplate what they’re talking about.”
Based on classified threat assessments, and concerns raised by DOE scientists, Brouillette urged NIAID to use caution in its collaborations with Chinese government scientists
DOE officials issued their most specific warning in mid-2019, just months before the pandemic began. Deputy Energy Secretary Dan Brouillette alerted a top Fauci adviser that the coronavirus research the US was helping to fund at the WIV risked being misappropriated for military purposes. Based on classified threat assessments, and concerns raised by DOE scientists, Brouillette urged NIAID to use caution in its collaborations with Chinese government scientists. His warning should have served as a red flag for any research the agency was conducting with China, according to two sources with knowledge of the exchange.
A spokesperson for NIAID said, “We are not aware of this interaction.” A spokesperson for Fauci, who has advised seven presidents on infectious disease policy and [supposedly] championed expanded treatment options for HIV and AIDS, said he was unavailable to respond to questions.
Shi Zhengli – dubbed the ‘Bat Lady’ or ‘Bat Woman’ for her work on bat coronaviruses – “investigated the possibility” Covid could have emerged from her lab back in 2020, according to colleagues. And you thought that little mask protected you?
Though the DOE and the NIH have partnered on historic endeavors, from the Human Genome Project to the Cancer Moonshot, they’ve also battled over what restrictions, if any, should be placed on technologies that allow scientists to synthesize and edit DNA. “We came at it from the point of view, ‘There are serious security concerns,’” says Ernest Moniz, who served as DOE secretary under Obama. “Our view was always, ‘We have to address them in ways that do not unduly restrict basic science.’ But what is the meaning of ‘unduly’? There lies the entire matter.” In meetings during the final months of the Obama administration, the longtime head of the NIH, Francis Collins, dismissed such risks as “science fiction,” according to several people present.
This June, the Office of the Director of National Intelligence (ODNI) issued a declassified report that provided a snapshot of perspectives on the COVID-19 origins question across America’s intelligence agencies. According to the report, the DOE and the FBI believe the pandemic is most likely to have originated with a lab leak. The National Intelligence Council and four other agencies say the virus most likely spilled over from a natural host, and two others, including the CIA, say there isn’t enough evidence to support one conclusion over the other.
All the intelligence agencies agree that SARS-CoV-2 was not developed as a bioweapon, the report said, and “almost all” agree it “was not genetically engineered.” Three sources said that DOE scientists, using an array of advanced tools and working out of several different labs, including Lawrence Livermore, Argonne, and Oak Ridge, could not rule out the possibility that the virus’s sequence had been engineered.
The ODNI report also found that People’s Liberation Army scientists sometimes worked out of WIV labs and collaborated with its civilian scientists on biosecurity projects and coronavirus research to address public health needs.
The Chinese government encourages such intermingling with a policy called military-civil fusion, which aims to harness civilian scientific innovation to advance military goals.
“This Reads Like a Movie Script”
In 2011, a Dutch virologist named Ron Fouchier announced at a scientific conference that he’d genetically engineered what he’d later describe as “probably one of the most dangerous viruses you can make.” He had altered the H5N1 avian influenza strain to make it transmissible among ferrets, which are genetically closer to humans than mice are. The experiment had been funded, in part, by the NIH.
Fouchier’s announcement triggered an uproar over what’s known today as gain-of-function research of concern—lab work that enhances the virulence or transmissibility of pathogens to help assess their threat to humans and develop countermeasures. Though the NIH has advocated for such research, others in the scientific community organized against it, arguing that creating pathogens that don’t exist in nature runs the risk of unleashing them.
The Dutch government initially blocked Fouchier from publishing his findings, for fear that they could serve as a how-to manual for bioterrorists.
Amid the controversy, the NIH assembled a high-level group, nicknamed the “ferrets committee,” to advise it on the risks of funding such research. As one member of the advisory group recalled, “We were worried we could be in violation of the Biological Weapons Convention.”
From 2009 to 2021, the NIH was led by Francis Collins, whose achievements include discovering the gene that causes cystic fibrosis. In March 2012, Collins wrote an email to members of the ferrets committee in which he acknowledged, “I am not familiar with the Biologic and Toxic Weapons Convention. Can our crack legal staff offer any opinions on this question?”
The Biological and Toxin Weapons Convention, enforced since 1975, is the most significant treaty that governs the development and use of biological agents.
In response, a staffer emailed her supervisor: “I can’t believe he doesn’t know what the BWC is???!!! yikes.” The supervisor replied, “It shows you how different our worlds are.”
In this study, which only allowed for the calculation of unadjusted observational associations, higher ORs were observed within the vaccinated versus unvaccinated group for developmental delays, asthma and ear infections.
Now odds are that there are other studies posted on the NIH that shows other incidents where the vaccinated children suffered greatly. Sadly we won’t know until there’s a Republican in the White House.
“The CDC has never looked at long-term health outcomes of vaccinated versus unvaccinated children,” attested Professor Brian Hooker, Ph.D., during a presentation to the World Council of Health.
After undergoing a full peer review, a newly published study in the European Journal of Heart Failure found that 1 in 35 people showed signs of heart damage after taking the Moderna COVID-19 vaccine.
The CDC openly admits that myocarditis and pericarditis (inflammation of the outer lining of the heart) are “rare side effects of COVID vaccination, especially prevalent in adolescents and young men.” Despite this serious concern, the CDC says the vaccine is safe for “the vast majority of people,” and that data shows “the low risk of complications from the vaccine is outweighed by the reward.”
The study concluded that adverse effects were more common than previously thought. The study also found that adverse effects were more frequent in women versus men.
“One in 35 health care workers at a Swiss hospital had signs of heart injury associated with the vaccine, mRNA-1273, researchers found,” according to the Epoch Times.
Researchers wrote in the paper, “mRNA-1273 booster vaccination-associated elevation of markers of myocardial injury occurred in about one out of 35 persons (2.8%), a greater incidence than estimated in meta-analyses of hospitalized cases with myocarditis (estimated incidence 0.0035%) after the second vaccination.”
“In a generally healthy population, the level would be about 1 percent, the researchers said,” the report found.
Adverse effects continued for a period of 30 days and half of the individuals showed unusually high levels of high-sensitivity cardiac troponin T, which is an indicator of subclinical heart damage.
The long-term implications of the study remain unclear as little research has tracked people over time with heart injury.
“None of the patients experienced a major adverse cardiac event, such as heart failure, within 30 days of booster vaccination, and none had electrocardiogram changes,” the report added.
The possible side effects of the COVID-19 vaccine have been a topic of controversy in recent weeks. Business mogul and Tesla boss, Elon Musk, responded to the heart attack of LeBron James’ son, Bronny, by questioning the role played by the experimental and controversial COVID-19 vaccine.
Musk responded bluntly, “We cannot ascribe everything to the vaccine, but, by the same token, we cannot ascribe nothing. Myocarditis is a known side-effect. The only question is whether it is rare or common.”
In recent years, Americans have witnessed an alarming increase in young and healthy people suffering cardiac arrest. The 18-year-old son of NBA superstar LeBron James was rushed to a hospital after collapsing during a basketball workout.
Social media erupted with widespread speculation about what caused Bronny’s heart to stop despite being a young and healthy athlete. In recent years, any questions or criticism surrounding the COVID vaccine are effectively censored, banned, and labeled “false” by the almighty truth-bearers on social media.
Multi-billion dollar pharmaceutical companies are also wielding their power, influence, and money to shape the national discourse surrounding their drugs. Twitter boss Elon Musk recently exposed internal documents proving Pfizer board member Dr. Scott Gottlieb helped censor Americans online.
“Nothing to see, no questions to ask,” Charlie Kirk sarcastically wrote.
Bronny is entering his first year at USC and he is ranked as a top-25 recruit and future NBA prospect by ESPN. A James family spokesperson said, “Yesterday while practicing Bronny James suffered a cardiac arrest. Medical staff was able to treat Bronny and take him to the hospital.” Bronny was discharged from the hospital after making a full recovery.
Here is the study. I’ll print the abstract and link to the article itself.
Sex-specific differences in myocardial injury incidence after COVID-19 mRNA-1273 booster vaccination
Natacha Buergin, Pedro Lopez-Ayala Contributed equally as co-first authors.
Abstract
Aims
To explore the incidence and potential mechanisms of oligosymptomatic myocardial injury following COVID-19 mRNA booster vaccination.
Methods and results
Hospital employees scheduled to undergo mRNA-1273 booster vaccination were assessed for mRNA-1273 vaccination-associated myocardial injury, defined as acute dynamic increase in high-sensitivity cardiac troponin T (hs-cTnT) concentration above the sex-specific upper limit of normal on day 3 (48–96 h) after vaccination without evidence of an alternative cause. To explore possible mechanisms, antibodies against interleukin-1 receptor antagonist (IL-1RA), the SARS-CoV-2-nucleoprotein (NP) and -spike (S1) proteins and an array of 14 inflammatory cytokines were quantified. Among 777 participants (median age 37 years, 69.5% women), 40 participants (5.1%; 95% confidence interval [CI] 3.7–7.0%) had elevated hs-cTnT concentration on day 3 and mRNA-1273 vaccine-associated myocardial injury was adjudicated in 22 participants (2.8% [95% CI 1.7–4.3%]). Twenty cases occurred in women (3.7% [95% CI 2.3–5.7%]), two in men (0.8% [95% CI 0.1–3.0%]). Hs-cTnT elevations were mild and only temporary. No patient had electrocardiographic changes, and none developed major adverse cardiac events within 30 days (0% [95% CI 0–0.4%]). In the overall booster cohort, hs-cTnT concentrations (day 3; median 5, interquartile range [IQR] 4–6 ng/L) were significantly higher compared to matched controls (n = 777, median 3 [IQR 3–5] ng/L, p < 0.001). Cases had comparable systemic reactogenicity, concentrations of anti-IL-1RA, anti-NP, anti-S1, and markers quantifying systemic inflammation, but lower concentrations of interferon (IFN)-λ1 (IL-29) and granulocyte-macrophage colony-stimulating factor (GM-CSF) versus persons without vaccine-associated myocardial injury.
Conclusion
mRNA-1273 vaccine-associated myocardial injury was more common than previously thought, being mild and transient, and more frequent in women versus men. The possible protective role of IFN-λ1 (IL-29) and GM-CSF warrant further studies.
How can this be? Antibodies Protect Against COVID-19 Reinfection. It’s good to see that the NIH at least admits that antibodies do work for those who had COVID. Their own study actually proves it. So why would the antibodies not work for those who haven’t had COVID?
In April of 2021 I had the one and done JJ jab and my antibodies and T-Cells have continued to go up. And guess what? No COVID. My family doctor and a scientist friend of his at Johns Hopkins both agree. We have this from the NIH.
About 3% to 4% of people with negative antibody tests got COVID-19 in each time period. But those who had antibodies were less likely to have COVID-19 as time went on. Only 0.3% of the people with antibodies had a positive COVID-19 test more than 90 days after. Those without antibodies were 10 times more likely to get the disease.
A man gets a monkeypox vaccine at a clinic in California on August 9, 2022. The Biden administration has seen an increase in vaccine lawsuits and is hiring more attorneys to handle the influx of cases.
PATRICK T. FALLON/AFP/GETTY IMAGES
The administration of President Joe Biden is hiring additional attorneys to help handle the workload from vaccine lawsuits after seeing a spike in people filing claims.
The COVID-19 pandemic thrust the potential side effects of vaccines into the spotlight, prompting fierce debate about whether the benefits outweigh the potential negative outcomes. While COVID vaccine side effects have been limited, several lawsuits from plaintiffs who have experienced adverse effects have attempted to hold pharmaceutical companies accountable.
A job posting on LinkedIn from the Department of Justice advertised for a trial attorney to specialize in cases related to the National Childhood Vaccine Injury Act. The legislation provides compensation to those injured by certain vaccines.
It’s unclear if the attorneys the Biden administration is hiring will be responsible for COVID-19 vaccine claims. COVID-19 vaccines are covered under the Countermeasures Injury Compensation Program (CICP), not the National Vaccine Injury Compensation Program (VICP), according to the Health Resources and Services Administration. Vaccines covered under the VICP include tetanus, measles, mumps and rubella, and polio.
Newsweek has reached out to the Department of Justice on Monday via media form for comment but did not receive a response in time for publication.
The position posted online advised applicants that they will have to handle heavy caseloads and work on cases that involve complex scientific issues that require expert witnesses. Since most cases are resolved without a trial, attorneys should be prepared to engage in settlement and damage negotiations, according to the posting.
A man gets a monkeypox vaccine at a clinic in California on August 9, 2022. The Biden administration has seen an increase in vaccine lawsuits and is hiring more attorneys to handle the influx of cases.PATRICK T. FALLON/AFP/GETTY IMAGES
Adverse side effects to the COVID-19 vaccine are rare, according to the Centers for Disease Control and Prevention (CDC), although some have died from them. Myocarditis, among the side effects, is most common in young males.
People who were negatively affected by the vaccine have expressed frustration with getting compensation from the U.S. government. In a recent lawsuit in Louisiana, plaintiffs called the process unconstitutional and a “black hole” in the judicial process. The lawsuit argues that the CICP provides “no timeline” for resolving their cases and one plaintiff had their case denied. The plaintiffs allege the COVID-19 vaccine led them to experience Bell’s palsy, brain blood clots, vascular inflammation and heart palpitations.
The CICP was created in 2005 and was used to deal with claims resulting from public health emergencies like anthrax exposure and the Ebola virus. It offers limited compensation, according to Reuters, and doesn’t have the option to provide compensation for damages or legal fees.
Unaccustomed to handling a large volume of cases, the program was flooded with more than 12,000 COVID-related claims. Only 32 had been deemed eligible for compensation and 1,129 had been denied as of October, according to Reuters.
Petitioners argued they didn’t have the opportunity to review evidence used against them or engage in other basic practices that would be afforded them in a trial. There are no hearings in CICP cases, and the decision is made by unidentified officials based on what a claimant submits.
Frustrations with vaccine injury compensation suits isn’t something unique to COVID claims. Attorneys and activists for years have been pushing for reform, pressing for the hiring of additional staff to handle the VICP cases. As of October, there was a backlog of nearly 4,000 claims, according to Bloomberg. Lawyers working on the cases hope Congress will pass legislation to reform how vaccine injuries are handled and for people to take action against pharmaceutical companies, not just the government.
“‘This is the first domino to fall,” David Carney, a Green & Schafle LLC attorney representing people injured by vaccines, told Bloomberg. “We’re going to start to see a windfall.”
Nearly two years before coronavirus became a household word, a National Institute of Health lab in Montana was conducting experiments with bats that focused on the spread of the virus.
The 2018 research was funded by the “Intramural Research Program of the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), and a research grant from NIH AID,” according to a report on the study available through the National Library of Medicine.
At the time, Dr. Anthony Fauci was the director of NIAID, a post he held from 1984 until his retirement in 2022.
The research was conducted at the Rocky Mountain Laboratories in Montana, which NIAID calls a “premier NIH facility for biomedical research.”
The experiment sought to determine whether the WIV1-coronavirus could infect and replicate in a group of 12 Egyptian fruit bats.
“They performed exams on the animals daily and measured things like body weight and temperature,” the Daily Mail reported. “Scientists also took samples from the bats’ noses and throats.
“On days three, seven and 28, four of the bats were euthanized and their heart, liver, kidney, spleen, bladder, reproductive organs, eyes and brain were collected for analysis. Scientists also analyzed white blood cell count and antibodies.”
The report on the experiment said that the virus was “unable to cause a robust infection” in the bats, later concluding that the spread of the virus could be specific to some bat species but not others.
Why isn’t Fauci in Jail?
The report also noted that existing research “suggests that a substantial portion of the SARS-like viruses circulating in bats cannot infect humans directly.”
COVID-19 was first reported in China in late 2019. Extensive debate has since raged whether the virus spread to humans through some as-yet-undiscovered animal pathway or was leaked from the Institute of Virology in Wuhan, China, where the outbreak was first noticed.
Fauci has scoffed at the lab-leak theory. He has also insisted that no “gain of function” research was approved on his watch. Such research is designed to increase the power of a virus to do harm to its host.
The bats for the 2018 project were obtained from the Catoctin Wildlife Preserve and Zoo in Thurmont, Maryland, the report said. The zoo is not far from the presidential retreat at Camp David.
The activist group White Coat Waste said the site has a history of animal care violations and called it a “crummy roadside zoo.”
Anthony Bellotti, the president and founder of White Coat Waste, denounced the project in a statement.
“Our investigation has uncovered the real-life horror story of how a shady roadside zoo whose curator was an NIH animal experimenter shipped off bats to a deadly government virus lab overseen by Dr. Fauci to be infected with a coronavirus obtained directly from the Wuhan lab that experts believe caused Covid,” he said, according to the Post Millennial.
Two studies, same results. No difference between Vaccinated and Non Vaccinated when it comes to infectiousness by vaccination status with Omicron variant. Medpage and the NEJ both had posted small studies. One on children, and one on adults. Both had the same results. No difference between Vaccinated and Non Vaccinated when it comes to infectiousness by vaccination status with Omicron variant.
The authors noted the results are consistent with a study in adults with the Omicron variant, which found no association between vaccination status and infectivity duration.
Posting the truth. What Tony the Fauch wouldn't tell us.
The Cleveland Clinic and others warned us on COVID. For several years we were being warned about COVID, and the Vaccine effectiveness. But the NIH and Tony the Fauch ridiculed and attacked anyone and everyone who disagreed with them.
These were men and women of Medicine and Science. Folks who did the actual research. Not Administrators who haven’t practiced for years. So I’ll give a few examples and links. You’ll find more in the comments section.
Summary Among 51017 working-aged Cleveland Clinic employees, the bivalent COVID-19 vaccine was 29% effective in preventing infection while the BA.4/5 lineages were dominant, and 20% effective while the BQ lineages were. Effectiveness was not demonstrated when the XBB lineages were dominant.
Conclusions Since the XBB lineages became dominant, adults “not up-to-date” by the CDC definition have a lower risk of COVID-19 than those “up-to-date” on COVID-19 vaccination, bringing into question the value of this risk classification definition.
Summary Among 48 344 working-aged Cleveland Clinic employees, those not “up-to-date” on COVID-19 vaccination had a lower risk of COVID-19 than those “up-to-date”. The current CDC definition provides a meaningless classification of risk of COVID-19 in the adult population.
From April 2023.
Conclusions
The bivalent COVID-19 vaccine given to working-aged adults afforded modest protection overall against COVID-19 while the BA.4/5 lineages were the dominant circulating strains, afforded less protection when the BQ lineages were dominant, and effectiveness was not demonstrated when the XBB lineages were dominant.
How do you defeat COVID misinformation from the left? You take them to court. It started back in 2020. Between March 2020 and July 2022, there were more than 1,000 court rulings on challenges to government orders and regulations designed to control the spread of Covid, according to Public Health Law Watch.
This from Politico.
Early in the pandemic, the Supreme Court blocked California and New York’s restrictions on religious gatherings to reduce Covid-19 transmission, as well as the CDC’s moratorium on evictions. In 2022, it stayed OSHA’s order that large companies require employees to be vaccinated or regularly tested for the virus. Federal courts have ruled against Biden’s Covid-19 vaccine requirement for federal employees and stopped the CDC’s mask mandate on public transportation. On March 31, a federal judge in Texas struck down the administration’s requirement that employees of Head Start programs be vaccinated.
But not just any court. Medical freedom activists have already started enjoying some successes in front of conservative judges. At the local level, several have sided with plaintiffs who’ve sued hospitals for refusing to give patients ivermectin. But it’s been on the federal level, with Trump-appointed judges, where they’ve enjoyed some of their most significant successes. In 2021, Texas Attorney General Ken Paxton sued the Biden administration over a proposed policy that would have required Covid vaccinations for all Head Start employees. In March 2023, Judge James Wesley Hendrix of the Northern District of Texas, a Trump appointee, struck down the proposed policy. In January 2022, a group of government workers sued the Biden Administration over the president’s vaccination requirements for all federal employees; in 2022, Judge Jeffrey Vincent Brown, whom Trump appointed in 2019, ruled in their favor. That ruling was briefly overturned, but in 2023, the 5th US Circuit Court of Appeals in New Orleans upheld it; the opinion was written by Trump appointee Judge Andrew Oldham.
In August 2022, a group of physicians sued the Biden Administration over its efforts to hold social media companies accountable for platforming physicians who spread misinformation about Covid. The plaintiffs, two of whom created the 2020 Great Barrington Declaration to oppose pandemic protections, accused the federal government of violating their First Amendment rights. “The US government used its vast power over social media and big tech to censor legitimate scientific and policy discussion about Covid during the pandemic,” Jay Bhattacharya wrote in a statement. That case is still ongoing, but in March, Trump-appointed judge Terry Doughty, in the Western District of Louisiana, denied a motion to dismiss it.
