‘Non-Starter’ to Authorize COVID-19 Vaccine for Infants: Dr. Peter McCullough
Moderna has requested the U.S. Food and Drug Administration (FDA) to grant an emergency use authorization (EUA) for its COVID-19 vaccine for children as young as 6 months. However, according to Dr. Peter McCullough, such authorization shouldn’t be granted because there’s almost no clinical benefit for children that young.
Pfizer is also working on data for a three-dose regimen after the FDA postponed its decision in February on whether to authorize its COVID-19 vaccine for this age group.
“I think for children that age, it’s a non-starter,” McCullough told NTD’s “Capitol Report” program on April 30.
McCullough said a recent study from New York State showed the efficacy of Pfizer’s COVID-19 vaccine in young children was so low that “it looks like they don’t work.”
The study (pdf) analyzed the Pfizer vaccine’s effectiveness in over 1.2 million fully vaccinated children in New York state from Dec. 13, 2021, to Jan. 30, 2022. Among those vaccinated children, over 852,000 were aged 12–17, and over 365,000 were aged 5–11.
“In the papers by [Vajeera] Dorabawila and colleagues from New York state, over a couple hundred thousand children aged 5 to 11, [had] virtually no clinical benefit, no vaccine efficacy. All the vaccine efficacy was less than 25 percent,” said McCullough, a renowned cardiologist and epidemiologist.
The study found that the vaccine effectiveness against infection declined from 66 percent to 51 percent for 12 to 17-year-olds and from 68 percent to 12 percent for 5 to 11-year-olds in about one and a half months.
The Pfizer vaccine is the only one currently being administered to children in this age group.
The FDA has said that vaccines should be at least 50 percent effective in preventing infection or decreasing disease severity to receive emergency authorization. The World Health Organization says vaccines are required to be 50 percent effective or better to receive clearance.
According to Moderna’s data, the vaccine was just 43.7 percent effective in the youngest group and 37.5 percent effective in the other children during the Omicron wave. Both were below the 50 percent bar. Some doctors and experts questioned that the trial result was not strong enough to warrant a EUA.
“That’s not acceptable by the FDA’s own standards,” Dr. Steven Hatfill, a virologist who advised the Trump administration, told The Epoch Times last month.
The FDA said it would thoroughly review Moderna’s request after additional data was provided.
“We have received a request from Moderna for a EUA for its COVID-19 vaccine for children 6 months to 6 years of age. As the company has acknowledged, they still need to submit additional data to complete its request. FDA cannot reach a decision on any vaccine without a completed EUA request, which allows us to do a thorough review, which includes, among other things, a comprehensive review of all of the adverse events and replication of the key analyses,” an FDA spokesperson told The Epoch Times in an email last week.
Some experts said it doesn’t make sense for young children to receive COVID-19 vaccines, as they are at low risk for severe disease and death from the CCP (Chinese Communist Party) virus, and the possible severe side effects are a big concern.
“Parents should think twice about vaccinating their child,” Dr. Robert Malone previously told The Epoch Times, adding that serious adverse events can occur, and most “are irreversible.”
Malone is a key contributor to mRNA vaccines, and his website includes a list of peer-reviewed studies related to COVID-19 vaccine adverse events in children, the main one being myocarditis.
In March, Florida’s top health official issued guidance, saying healthy children may not benefit from receiving current COVID-19 vaccines.
“Based on currently available data, the risks of administering COVID-19 vaccination among healthy children may outweigh the benefits,” Florida Surgeon General Dr. said in a statement. “That is why these decisions should be made on an individual basis and never mandated.”
The Centers for Disease Control and Prevention (CDC) has been saying that COVID-19 vaccines are safe and effective, and severe side effects are rare. The agency also says that all children aged 5 and older should get Pfizer’s vaccine, and all children between the ages of 12 and 17 should get a booster.
However, recent studies have found that Pfizer’s COVID-19 vaccine doesn’t do well in preventing infection against the Omicron variant for children 5 to 15 years old.
McCullough pointed out that it would be unnecessary to get young children vaccinated because most of them have already contracted the virus.
“We’ve heard reports recently from the CDC that roughly 75 percent of children have already had COVID. So for them, it’s too late for any hope of a vaccine. The vaccine can’t help once somebody’s already had COVID,” McCullough said, adding that if a vaccine doesn’t have at least 50 percent coverage, it would be considered “nonviable.”
On April 26, an early release of CDC’s Morbidity and Mortality Weekly Report said that about 75 percent of children and adolescents had already developed antibodies against the disease.
McCullough said COVID-19 has become “progressively” milder through its progression of mutations and the Omicron variant caused much fewer hospitalizations or deaths.
A number of studies have found that the clinical severity of infection is much lower for Omicron than for the Delta variant. In March, a peer-reviewed study published in Lancet is the largest one to date, which analyzed data from 1.51 million COVID-infected people in England between November 2021 and January 2022. Among them, over 1.06 million were infected by Omicron.
The study found that the overall risk of hospitalization within the 14 days after a positive test was 1.64 percent with Delta and 0.9 percent with Omicron. The mortality risk in the 28 days after a positive test was 0.27 percent after Delta, falling to 0.11 percent after Omicron.
“I can tell you, we have studies now, large studies on Omicron, where there’s close to zero hospitalizations or deaths,” said McCullough. “It’s essentially a common cold.”
The Epoch Times has contacted FDA, Moderna, and Pfizer for comments.
https://www.theepochtimes.com/non-starter-to-authorize-covid-19-vaccine-for-infants-dr-peter-mccullough_4447924.html
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FDA: Americans Should Treat COVID-19 Like the Flu
Several top Food and Drug Administration (FDA) officials, including Commissioner Robert Califf, admitted that Americans will now have to accept COVID-19 as another respiratory virus, comparing it to influenza.
Califf, Principal Deputy Commissioner Janet Woodcock, and top vaccine official Dr. Peter Marks wrote for the Journal of the American Medical Association that COVID-19 will be around for the foreseeable future while suggesting that it will require yearly vaccines targeting the most threatening variations of the virus.
“Widespread vaccine- and infection-induced immunity, combined with the availability of effective therapeutics, could blunt the effects of future outbreaks,” the officials said, referring to another name for the CCP (Chinese Communist Party) virus. “Nonetheless, it is time to accept that the presence of SARS-CoV-2, the virus that causes COVID-19, is the new normal.”
The virus “will likely circulate globally for the foreseeable future, taking its place alongside other common respiratory viruses such as influenza. And it likely will require similar annual consideration for vaccine composition updates in consultation with the [FDA],” they continued.
It’s a departure from the rhetoric that was expressed by public health officials in 2020 and 2021. In late October 2020, for example, current White House COVID-19 adviser Anthony Fauci said that President Donald Trump’s comparisons to the flu were false, telling NBC at the time “it is not correct to say it’s the same as flu.”
About a year later, Fauci told CBS News that Americans will “likely” have to deal with COVID-19 in a similar manner as influenza. “That’s entirely conceivable and likely, as a matter of fact, we are not going to be in a situation of this degree of intensity indefinitely,” he said when asked about the Omicron variant.
Data published by the U.S. Centers for Disease Control and Prevention (CDC) shows that while cases have trended slightly upward in the United States, the numbers are a fraction of the cases that were reported in mid-January when the seven-day average stood at around 800,000 per day. As of May 6, the seven-day average was about 68,000 per day.
In the Journal of the American Medical Association article, the three FDA officials proclaimed that by the summer of 2022, decisions will have to be issued “about who should be eligible for vaccination with additional boosters and regarding vaccine composition.”
“Administering additional COVID-19 vaccine doses to appropriate individuals this fall around the time of the usual influenza vaccine campaign has the potential to protect susceptible individuals against hospitalization and death, and therefore will be a topic for FDA consideration,” they added.
https://www.theepochtimes.com/fda-americans-should-treat-covid-19-like-the-flu_4453370.html
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When Biden’s own people don’t trust him to speak, we have no real president
There is nothing more symbolic of American political power than a president of the United States holding court in the Oval Office.
Ensconced in that intimidating room, countless leaders have browbeaten, charmed, and cracked wise with the powerful and the press for generations.
But not Joe Biden.
And now we know why. According to new reporting, the reason we don’t see Joe in the Oval very often is that his team can’t install a teleprompter to keep the gaffer-in-chief on script.
So yeah, that’s where we are regarding the leader of the free world.
If one really stops and thinks about this it is simply shocking. The primary job of any politician, but especially a president, is to communicate a vision of policy and competency to the American people and the people of the world.
We have a president today who is incapable of this most basic element of his job. And whatever unelected group of White House flunkies there are — who are actually the president — can’t trust him to even open his mouth unless he can stare at a teleprompter and mouth their insights like the weatherman.
Things have gotten so obvious and awkward of late that even when Biden does have his trusty large print screen scrolling his supposed ideas he can’t even push them out. His struggle with the word “kleptocracy” in recent remarks was just sad. And fine, he grew up with a stutter, but he’s been in the public spotlight since “The Godfather” was in movie theaters.
The darkest and most troubling possibility here, but one we must face, is that we functionally have no actual President of the United States. If he can’t appear in public, in his own office, for want of a digital cheat sheet, then of course he has little if anything to do with the actual running of the country. And he’s not even a good false figurehead — using the teleprompter he often looks and sounds like he’s reading the bottom line of the eye exam.
Let’s face it. Even for an administration that thinks it’s a TV show, the construction of a White House set where Biden can wax incoherently was bizarre. But now we know this sound studio was set up to protect Biden, as much as possible, from his own words and actions. Maybe soon the president will only do live events in virtual reality where his handlers can correct his errors in deep fake real-time. Why not have the president be a programmed hologram? Is that so different from the current reality?
It’s time to talk about grandpa. He probably shouldn’t be driving or using the gas oven on his own anymore, or, you know, running the most powerful country on the planet into the ground.
Maybe the White House will overcome the great technical challenges of getting a screen with words on it into the Oval Office and we can once again see a president in his actual, natural environment. But given that this administration has given no indication in 20 months that it can even tie its shoes, I suggest we don’t hold our breath.
Pay no attention to the man behind the curtain, the wonderful Wizard of Ahs and Ums. Just go along with the joke as the Democrats would have us do. But the joke isn’t funny anymore. A president who cannot even give brief remarks in the Oval Office is no president. And that, my friends, is that sad fact.
So what are we going to do about it?
https://nypost.com/2022/05/06/when-bidens-own-people-dont-trust-him-to-speak-we-have-no-real-president/
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)
http://australian-politics.blogspot.com/ (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com/ (TONGUE-TIED)
https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)
https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)
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10 May, 2022
Whistleblower Exposes 3 Big Issues in Pfizer’s COVID Vaccine Clinical Trials
On Nov. 2, 2021 British Medical Journal (BMJ) published an article that revealed three big issues in Pfizer’s vaccine trial based on interview with a whistleblower.
The whistle blower, Brook Jackson, was a regional director of one of Pfizer’s vaccine trial companies, Ventavia Research Group in Texas.
Beginning the fall of 2020, there were 153 institutes, including Ventavia, that assisted Pfizer’s vaccine clinical trial. Per Ventavia’s website, the company is the largest private clinical research company in Texas. Jackson found out the management of the clinical trial in the company was not organized. She reported this to the administrative level of the company, but received no response from the company. Then she reported this to the FDA.
However, after she emailed the FDA, she was fired that same afternoon. Jackson said this was the first time she was fired from her job in her 20-year career.
Finally, she contacted the international well-known journal–BMJ. She exposed 3 major issues she observed in Ventavia for Pfizer’s vaccine clinical trial.
1. Falsifying the data
2. Early unblinding of the trial, affecting the accuracy of the results
3. Very slow to respond to adverse events, and not paying attention to the safety of participants
We spoke with Dr. Sean Lin, phD, former toxicology lab director of Walter Reed Military Medical Center to discuss these issues. The interview below has been edited for brevity and clarity.
Issue 1: During the Trials, There Was Data Falsified
Health 1+1: Per Jackson, in one document dated as August 2020, before Jackson’s hiring, a Ventavia executive revealed that three site staff members were requested to go over e-diary issues and falsifying data, etc. One of them was verbally questioned for changing data and not informing the late data entry.
Jackson and Ventavia executives discussed multiple times the possibilities of an FDA inspection of their company. Another former Ventavia employee also stated that the company worried the FDA would audit the process of their company’s Pfizer’s vaccine clinical trials.
Dr. Lin: When any new vaccine or new medication goes through clinical trials, the accuracy of the data is very important.
For example, in clinical trials, to inject vaccine to a volunteer, there must be 2 people in addition to the volunteer on site. One person does the injection; the second person takes notes and watches the injection. The reason for having two people is if only one person does it, if there is any mistake in recording the procedure, or if the person changes data, the accuracy of the database will be affected significantly.
In cases where any data needs to be modified, these drug companies usually have strict procedures. First, upper management and an executive of the drug company need to be notified and approve, then the person is authorized to enter the database and modify the data. The person must record the time of modification and the reason. They need to explain that an error occurred while entering the data, or if there are other reasons. Only with strict rules can these companies guarantee that what is in the database won’t be falsified.
So by contrast, it is unbelievable that an employee at Ventavia can have the right to modify the database without permission. This can cause big problems.
Pfizer published their clinical trial report on NEJM (New England Journal of Medicine). In the report, there were 8 people infected COVID after vaccination, but there were 162 people infected COVID after placebo. So, it is easily to change the protection rate from 90% to 60% if there are wrong data on dozens of people.
Ventavia’s trial site had 1,000 volunteers participate in the COVID vaccine trials. If there are mistakes in just 50 of them, the results will be significantly different.
Issue 2: Early Unblinding of Trial Participants
Health 1+1: Based on the photos and information provided by Jackson, documents related to the clinical trials were randomly displayed, including vaccine packaging materials with clinical trial participants’ information and drug assignment confirmation labels, all these were accessible to blinded personnel. The above errors can lead the participants and the staff members to know ahead of time who would get vaccine, before the procedures were done. The errors were corrected two months after the trial started. It may have been a large range of unblinding.
Dr. Lin: Generally, people who participate in clinical trials are divided into two groups. One group would receive vaccine and the other group would receive placebo, like normal saline. None of the participants will know which they were given, otherwise it would affect the objectivity of the trial. This is called blinding.
Vaccine trials routinely use blind trials. This is because in medical field, it is well known that the mental effect plays a key role. For example, if someone knew he or she was given real medicine, they may have very positive mood which improves their immune system, and the results would not truly reflect the effect of medicine only. On the other hand, if people knew they were given placebo, they may not feel any hope, and that may also affect the results.
Besides the volunteer participants, other people who involved in the trials like physicians, nurses, and people who man database are also not allowed to know the true information regarding the distribution of the vaccine injection. This is to avoid bias. For example, if the nurse knew the participants receiving vaccine, the nurse may pay more attention to the person. This will affect the end results.
So the clinical trials are randomly assigned by computer for who receives the vaccine and who receives the placebo, and the information will be encrypted.
For early unblinding, it was not only a lapse in responsibility on Ventavia’s part, but showed problems related to Pfizer’s design and management of these COVID vaccine clinical trials. This made it so that the testing groups learned who was getting the vaccine too early. If lower level staff have authority or opportunity to unblind trials, it affects the objectivity of the data.
Issue 3: Slow Response to Adverse Events, Not Prioritizing Participant Safety
Health 1+1: Jackson pointed out that Ventavia did not pay attention to the safety of the participants during the vaccine trials. They did not contact or take care the participants who developed side effects. One email sent by the contract research organization to Ventavia mentioned that over 100 cases with issues where participants were not contacted for more than three days, including including two participants who had developed severe symptoms. The expectation for vaccine trials is that that all issues need to be addressed within 24 hours. Jackson also mentioned that participants were placed in a hallway after injection with no clinical staff observation.
Besides Jackson, a formal Ventavia employee also told the BMJ that the company doesn’t have enough staff to take samples from participants who developed COVID symptoms. FDA documents showed that across all clinical trials, there were 477 people who had symptoms but did not receive a PCR test for COVID. Jackson said in the 40-plus clinical trials she’s been involved with, including several large scale trials, she had never seen as much chaos as the environment she worked in under Ventavia.
In a recording of a meeting in September 2020 between Jackson and two Ventavia company directors, the company expressed they could not confirm how many types of issues had occurred because of the high volume of issues, nor could they confirm the number of errors that had occurred because there was something new everyday.
Dr. Lin: In clinical trials, the risk of the medication given to participants is unknown, and as such there needs to be enough staff to watch for side effects that could occur.
Usually, participants stay onsite, whether that is a hospital or nearby hotel, for the first 24 hours after the vaccine injection, and they are accompanied by clinical staff. If a severe side effect occurs, it needs to be addressed right away. It is dangerous if no one is observing the participants after injection. This suggests the trial was not properly staffed.
In the past, there were clinical trials for certain medications that took a very long time before they could even begin. First you need to have enough test sites, then the standard data criterion needs to be set up to ensure the data integrity and security, among other things. If you have contractors with the capacity to test 500 people, but you sign them for contracts to test 1000 people, obviously they will have staffing and staff training issues. There’s a standard protocol that accompanies each step of these clinical trials and no short cuts can be taken, even if a pharmaceutical company wants to speed up the testing period. In this case specifically, Pfizer would have needed to monitor these testing sites, in order to ensure all these trials are using their designed process.
Ventavia’s situation implies additional risks, like the possibility of other sites having similar issues, and whether Pfizer has been correcting these in a timely manner. If the vaccine data contains errors, then wouldn’t the vaccine’s protection rate need to be reevaluated?
During the pandemic, many large pharmaceutical companies received protection from government. The entire vaccine development bill was footed by the government, as was the production and promotion costs. And even if there were problems in the process, the media was not investigating these steps and exposing the details to the public.
Pfizer’s vaccine has been so important in the US market and stricter monitoring should have been in place, rather than blanket protections.
FDA’s Poor Oversight
Health 1+1: Jackson reported the issue to the administrative level of Ventavia and received no response. Then on Sept. 25, 2020, she contacted the FDA. After sending the email, she was fired from the company. A few days later, the FDA contacted Jackson to discuss her report. There was no further communication between Jackson and the FDA after this call. In August 2021, the FDA approved Pfizer’s COVID vaccine and listed 9 of the 153 clinical trial sites, not including Ventavia.
Jackson raised several problems in her report:
1) Participants were not monitored after receiving injections
2) There was no timely follow-up of patients with adverse side effects
3) Errors occurred during testing, and people would not report the errors
4) The vaccines were not stored at proper temperatures
5) Mislabeled laboratory specimens
6) Staff who reported these types of problems received retaliation
7) FDA told her no further information could be provided to her and ceased communications, and only nine of 153 test sites were inspected by the FDA, not including Ventavia, despite Jackson’s report
This exposes the oversight issues on the FDA’s part. In Ventavia case, FDA should have communicated with Jackson, Pfizer, and Ventavia. It stands that the FDA should have inquired about Pfizer’s trial procedures, and whether these three parties were on the same page regarding those procedures. And the public should have been made aware, because this affects human lives.
Dr. Lin: It’s more than an issue of corporate liability, there’s a matter of individual responsibility here as well. This whistleblower’s report showed that it wasn’t just Ventavia in the wrong, but Pfizer and the FDA as well. But I think the key issue is still the individual, because you have to remember that these are individuals doing all the research.
Many people think that science is noble, and all the people who work in the scientific field are pursuing truth. But in reality, in modern society, science is an industry. Especially the medical field, it’s become a large industry that involves huge profits. So in the process, the issue of how to keep research and clinical trials reliable and trustworthy has become a big challenge.
During the pandemic, the public had hope that pharmaceutical companies would develop medicine that could save lives. There’s a big profit opportunity here for the companies, especially because the government will help cover costs and also promote the products. With an upside this big, no company wants to miss out. With these conditions, it’s easy to risk the integrity of the company. Especially under the current PREP regulations, the company doesn’t take any responsibility. Pfizer and Moderna are free of responsibility involving this vaccine. People with adverse side effects from these injects can seek compensation through CICP, but it is not easy to do.
According to a Nov. 10, 2021 report from USA Today, 3,100 people developed side effects after vaccine injection during clinical trials. Following the CICP system, they filed for reimbursement, and none of them have thus far received compensation.
The government pays for production and protection, and the companies don’t need to pay out any losses from side effects. Big profits with small investments. Under these conditions how can one guarantee the integrity of the test? It in fact motivates the companies to rush their clinical trials. These are complicated procedures with many factors that can cause issues. Pharmaceutical companies should be following the basic principle of “do no harm.” Without this principle, the medical field is in peril.
Both the government and pharmaceutical companies have been focusing on the benefit rather than the drawbacks. This is a problem, because it means that something that could put someone’s life at risk can be ignored. This is irresponsible to the public.
On one hand, during a pandemic, ordinary people would of course wish that medical companies could develop medicine to save the world. Can pharmaceutical companies keep a high level of integrity through the process? I think this is a test for humanity arranged by God.
If humanity handles this test well, God creates miracles to help humanity.
If, under what is deemed an emergency condition, in the name of saving people at large a government decides to risk some people’s lives in trade, that is not right. Just like in China, the regime is behind the operation of organ harvesting ordinary citizens to make a profit. If a surgeon in China claims he saved a life through organ transplantation but had to kill another human being to do so, that is totally wrong.
Whether a physician or pharmaceutical expert, whether you can maintain morality and integrity during this pandemic is a test from God. As COVID spread across the entire world, it’s become a test not only to the medical field but all human beings.
https://www.theepochtimes.com/whistleblower-exposes-3-big-issues-in-pfizers-covid-vaccine-clinical-trials_4440371.html
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)
http://australian-politics.blogspot.com/ (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com/ (TONGUE-TIED)
https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)
https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)
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9 May, 2022
Won’t Get Fooled Again
More than a century ago, Mark Twain identified two fundamental problems that would prove relevant to the Covid pandemic. “How easy it is to make people believe a lie,” he wrote, “and how hard it is to undo that work again!” No convincing evidence existed at the start of the pandemic that lockdowns, school closures, and mask mandates would protect people against the virus, but it was remarkably easy to make the public believe that these policies were “the science.” Today, thanks to two years of actual scientific evidence, it’s clearer than ever that these were terrible mistakes; yet most people still believe that the measures were worthwhile—and many are eager to maintain some mandates even longer.
Undoing this deception is essential to avoid further hardship and future fiascos, but it will be exceptionally hard to do. The problem is that so many people want to keep believing the falsehood—and it’s not just the politicians, bureaucrats, researchers, and journalists who don’t want to admit that they promoted disastrous policies. Ordinary citizens have an incentive, too. Adults meekly surrendered their most basic liberties, cheered on leaders who devastated the economy, and imposed two years of cruel and unnecessary deprivations on their children. They don’t want to admit that these sacrifices were in vain.
They’re engaging in “effort justification,” a phenomenon famously demonstrated in 1959 with an experiment involving a tame version of a hazing ritual. Social psychologists Elliot Aronson and Judson Mills offered female undergraduate students a chance to join a discussion group on the psychology of sex, but first some of them had to pass an “embarrassment test.” In the mild version of the test, some students read aloud words like “prostitute” and “petting.” Others had to pass a more severe version by reading aloud from novels with explicit sex scenes and lots of anatomical obscenities (much more embarrassing for a young woman in the 1950s than for students today). Afterward, all the students, including some who hadn’t been required to pass any test, listened in on a session of the discussion group, which the researchers had staged to be a “dull and banal” conversation about the secondary sexual behavior of lower-order animals. The participants spoke haltingly, hemmed and hawed, didn’t finish their sentences, mumbled non sequiturs, and “in general conducted one of the most worthless and uninteresting discussions imaginable.”
But it didn’t seem that way to the women who’d undergone the severe embarrassment test. They were far more likely than the other students to give the discussion and the participants high ratings for being interesting and intelligent. The experiment confirmed the then-novel theory of cognitive dissonance: the young women didn’t like thinking that they’d gone through an ordeal for the sake of a worthless reward, so they avoided this mental discomfort (cognitive dissonance) by rewriting reality to justify their effort. Other studies showed the same effect in people who had undergone real-life initiation rituals to join fraternities and other groups. The more effort involved in the initiation ritual, the more valuable seemed the reward of membership.
Researchers also reported that “shared dysphoric experiences” produced “identity fusion” within a group, making members more loyal and more willing to make further sacrifices for their comrades. Thus, fans of English soccer teams who suffered together through a losing season were more devoted to one another than were fans of a winning team, and members of Brazilian jujitsu clubs who endured a painful graduation ceremony—walking a gauntlet while being whipped by belts—became more willing to make charitable donations to their club than were members at similar clubs with less extreme ceremonies.
If one brief bad experience can transform people’s thinking, imagine the impact of the pandemic’s ceaseless misery. It’s been a two-year-long version of Hell Week, especially in America’s blue states, with Anthony Fauci and Democratic governors playing the role of fraternity presidents humiliating the pledges. Americans obediently donned masks day after day, stood six feet apart, disinfected counters, and obsessively washed their hands while singing “Happy Birthday.” They forsook visits to friends and relatives and followed orders to skip work and church. They forced young children to wear masks on the playground and in the classroom—a form of hazing too extreme even for Europe’s progressive educators.
Some Americans refused to submit to these rituals, but their resistance only intensified solidarity among the faithful. The most zealous kept their masks on even after they were vaccinated, even when walking alone outdoors. The mask became their version of a MAGA hat or a fraternity brother’s ring; some have vowed to keep wearing theirs long after the pandemic. They’ve already called for permanent masking on airplanes, trains, and buses, and they’ll probably clamor for more school closures and lockdown measures during future flu seasons.
Facts alone will not be enough to change their minds. To undo the effects of the hazing, we need to ease their cognitive dissonance by showing that they’re not to blame for their decisions. The mental mistakes were not made by citizens who dutifully sacrificed for two years. They assumed that the Centers for Disease Control knew how to control disease and that scientists and public-health officials would provide sound scientific guidance about public health. Those were reasonable assumptions. They just turned out to be wrong.
After a great disaster, the traditional response is to appoint a blue-ribbon panel to investigate it, and a bill has already been introduced in Congress to create a Covid commission. In theory, this could be a worthy public service, allowing experts to sift the evidence impartially and determine which strategies worked, which ones failed, how much needless damage was done—and whom to blame for it. But in practice, which experts would the current Democratic administration or Congress appoint? Presumably, the pillars of the public-health establishment—the same luminaries whose advice was followed so calamitously the past two years.
“CDC leaders used unrealistic projections to claim unprecedented powers and experiment with untested strategies.”
Before Covid, the United States drew up plans for a pandemic and maintained the world’s most lavishly funded scientific and medical institutions to deal with one. When the coronavirus arrived, the leaders of those institutions should have identified who was at serious risk and who wasn’t and adopted proven strategies to protect the vulnerable while doing the least harm to everyone else. They should have monitored the effects of their policies and adjusted them based on what they learned. By honestly communicating the risks and considering the overall public good, they could have tamped down needless fear and united the country behind their efforts.
Instead, they proceeded to ignore their own plans as well as the basic principles of science and public health. Leaders of the CDC terrified the public with worst-case scenarios based on computer models—and then used those blatantly unrealistic projections to claim unprecedented powers and experiment with untested strategies. Their pre-Covid planning scenarios had rejected business and school closures even for a pandemic as deadly as the Spanish flu of 1918, but when the Covid-19 pandemic came, they imposed lockdowns without even pretending to weigh the hypothetical benefits against the tangible economic, medical, and social costs—not to mention the intangible costs in emotional hardship and lost liberty. Randomized clinical trials conducted before the pandemic had repeatedly shown that masks did little or no good at preventing viral spread, but the CDC proclaimed them effective against Covid and promoted mask mandates nationwide. As the pandemic wore on, federal health officials looked for excuses to justify the lockdowns and mandates, hyping flawed studies and cherry-picked data, while failing to sponsor rigorous research testing their strategies.
They stubbornly ignored the hundreds of studies around the world showing that, except in a few isolated places, lockdowns did not reduce Covid mortality and that mask mandates were generally ineffective and senselessly cruel in classrooms. The most glaring evidence came from places with the least restrictive policies, like Florida, along with the Nordic countries Sweden, Finland, and Norway, which avoided lockdowns and mask mandates—yet did as well as, or better than, the average in preventing both Covid deaths and overall mortality during the course of the pandemic.
Instead of heeding all this evidence of their mistakes, federal officials did their best to suppress it and silence dissenters. Francis Collins, the head of the National Institutes of Health, wrote to Anthony Fauci in October 2020 urging “a quick and devastating published takedown” of the “three fringe epidemiologists” responsible for the Great Barrington Declaration. These three researchers—from the “fringe” institutions of Harvard, Stanford, and Oxford—criticized the deadly harms of the lockdowns and urged an alternative strategy of focusing protection on the high-risk elderly, allowing natural immunity to grow among the younger population at low risk. Fauci and Collins went on a media offensive, dismissing the focused-protection strategy as “very dangerous” and “not mainstream science.” Other scientists quickly joined the attack on the Great Barrington Declaration by signing a rebuttal, the John Snow Memorandum, which asserted that lockdowns were effective and dismissed the idea of natural immunity, claiming that “there is no evidence for lasting protective immunity to SARS-CoV-2 following natural infection.”
It was a remarkably irresponsible claim, given already-existing evidence at the time (the fall of 2020) that people’s immune systems developed defenses after a Covid infection. It would have been surprising if an infection didn’t produce durable protection. Yet this denial of natural immunity appeared in The Lancet and was signed by thousands of scientists and doctors, including Rochelle Walensky, who enshrined this unscientific notion as CDC policy when she became the agency’s leader during the Biden administration. It didn’t matter that natural immunity was repeatedly shown to be stronger and longer-lasting than vaccine immunity, or that other countries exempted people with natural immunity from vaccine mandates. The Biden administration insisted on vaccinating everyone—and firing workers who refused, including hospital staff and other essential workers whose prior Covid infections gave them stronger immunity than their vaccinated colleagues. Instead of uniting Americans against the virus, public-health officials chose painful policies that divided the faithful from the disobedient.
The public needs to learn what went wrong during the pandemic, but they’re not going to hear it from the Biden administration. It rewarded Fauci for his failures by giving him a new title, Chief Medical Advisor to the President, and would surely resist any serious investigation of its Covid strategies. Republicans could start the process if they win control of Congress in November and establish a Covid commission, but they’d be taking on the federal bureaucracy as well as the public-health establishment. Scott Atlas, the health-policy analyst from the Hoover Institution who joined the Trump administration’s Covid task force and fought unsuccessfully against Fauci’s pandemic policies, says that his experience in Washington has convinced him that any government-run commission would be a mistake.
“It’s massively naïve to think that our government will do anything objective,” Atlas says. “Any U.S. government panel would be viewed as, or be in reality, 100 percent partisan. It could be smarter to have an international organization do it, looking at the overall questions of management, because if it’s only an assessment of the U.S., then it naturally becomes a political blame game.” But which international organization could be trusted to do a fair investigation? The obvious candidates, like the World Health Organization or the World Bank, would presumably rely on establishment figures loath to admit their mistakes. And even if they honestly evaluated the pandemic strategies, how much impact would the report have? The mainstream press would probably either ignore it, as it ignored a recent meta-analysis concluding that lockdowns had “little to no effect” on Covid mortality, or attack it with the same tactics used to smear the Great Barrington Declaration as “not mainstream.”
The Great Barrington scientists’ ideas about focused protection and natural immunity have been vindicated—unlike the counterclaims and unproven strategies promoted in the John Snow Memorandum—but these researchers were no match for their media-savvy opponents, as Stanford’s John Ioannidis recently concluded after analyzing the credentials of the two sides. By considering how often the scientists’ research had been cited in the scientific literature, he found that the signatories of the Great Barrington Declaration included just as many top-cited scientists as did the signatories of the John Snow Memorandum. But there were a few crucial differences: the Snow signatories had many more Twitter followers, and they received a lot more attention on Twitter than in the scientific community. They had the dubious distinction of scoring much higher on a scale called the Kardashian index, named after the celebrity Kim Kardashian, which measures the discrepancy between a scientist’s social-media footprint and the citation impact of the scientist’s research. Twitter enabled activist scientists to exert an outsize impact on the public debate over Covid strategies. The lockdowns and mask mandates came to be perceived as “the science,” parroted by the mainstream press and enforced by censors on social-media platforms.
The activists kept pretending that those strategies worked, but their narrative became harder to sustain. Surveys by the Pew Research Center showed that the public’s trust in scientists rose at the start of the pandemic and then began falling. The earliest and steepest declines occurred among Republicans, so that today only 15 percent of Republicans have “a great deal of confidence” in scientists—while more than a third have “not too much” or “none at all.” Democrats remain far more trusting, but even their confidence in scientists is now lower than at the start of the pandemic.
“Public trust in science is over unless there’s a thorough review of the pandemic policies,” says Jay Bhattacharya of Stanford, one of the Great Barrington Declaration scientists. Unlike Atlas, he believes that a federal Covid commission could serve a purpose. “The harms of the lockdowns are so obvious, and the failure to protect the vulnerable so obvious, that it would be hard for a commission to whitewash the facts. It’s going to take political will, but it needs to be done to restore trust in public health.”
For now, the best opportunity for a public airing of the facts may be the 2022 election campaign. Some candidates are already attacking the lockdowns and mask mandates, and pandemic strategies could become a major issue in the 2024 presidential race, especially if Ron DeSantis runs on his success as Florida’s governor.
https://www.city-journal.org/after-pandemic-americans-must-never-surrender-core-liberties-again
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)
http://australian-politics.blogspot.com/ (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com/ (TONGUE-TIED)
https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)
https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)
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8 May, 2022
Sweden’s Covid death rate among lowest in Europe, despite avoiding strict lockdowns
Sweden’s death rate during the Covid pandemic is among the lowest in Europe, despite the country refusing to impose strict lockdowns, according to new figures from the World Health Organisation.
The UN health agency released estimates of excess deaths - people who died directly and indirectly from Covid - showing the pandemic had wrought a “staggering toll” worldwide, with 14.9 million fatalities, three times higher than fatalities officially reported.
Britain, according to the new data, had a lower excess death rate than Spain, Germany and Italy.
Experts said the difference demonstrated stringent lockdowns alone did not determine success when battling Covid-19.
The WHO analysis includes deaths directly linked to Covid but also indirect fatalities - including those unable to access healthcare for other conditions while services were overwhelmed or suspended.
It also accounts for deaths averted during the pandemic, for example because of the lower risk of traffic accidents during lockdowns.
Sweden, which was criticised in the early stages of the pandemic for resisting a mandatory lockdown, had fewer deaths per capita than much of Europe.
In 2020 and 2021, the country had an average excess death rate of 56 per 100,000 - compared to 109 in the UK, 111 in Spain, 116 in Germany and 133 in Italy.
Low obesity rates a factor
Although Sweden fared worse than its Nordic neighbours, lower rates of obesity - a key risk factor for severe coronavirus disease - and a better-resourced healthcare system helped limit fatalities in the country.
“The lesson from Sweden is to invest in your population's health and have less inequality,” Prof Devi Sridhar, the chairman of global public health at the University of Edinburgh, told The Telegraph.
She said that although the UK’s initial response was weak, the country “definitely did better post-vaccine rollout than other places”, which contributed to a lower excess death rate overall.
Dr Michael Head, a senior research fellow in global health at the University of Southampton, added: “There have been too many preventable deaths here in the UK during the pandemic. However, early rollout of the vaccines, including the booster doses, will also have averted many deaths.
“By the end of the pandemic, it's likely that the UK will probably end up mid-table on various metrics that measure pandemic performance, such as excess mortality,” he told The Telegraph.
Meanwhile some countries - including Australia, New Zealand and Japan - actually reported negative excess death rates, suggesting there were fewer fatalities than expected during 2020 and 2021.
The global disparity between official figures and excess deaths is not a surprise. Even before the pandemic, around six in 10 deaths globally went unreported.
The WHO said that middle-income countries - where both Covid testing and death registrations are patchy - account for 81 per cent of excess deaths in the first two years of the pandemic, compared to just 15 per cent in high-income nations.
Dr William Msemburi, an WHO official, added that the vast majority of deaths - some 68 per cent - were centred in just 10 countries, which include the United States, Russia and India.
https://www.telegraph.co.uk/global-health/science-and-disease/swedens-death-rate-among-lowest-europe-despite-avoiding-strict/
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Why SOME people are 'unicorns' who will NEVER get Covid while others are infected over and over again - and others don't even know they've had it
I may be one of the "unicorns". I have had exposures that should have given Covid to me but I have had zero symptoms. My good experience could be due to the fact that I have had two shots of the AstraZenica vaccine But I was rather late in getting the vaccine and had "dangerous" exposures first without getting anything. Unlike many people I also got no perceptible side-effects from the vaccine
When James Cruickshank tested positive for Covid-19 this year, his girlfriend automatically assumed she was next. The 30 year-old fitness fanatic and his partner, Steph Grant, live together in a rented apartment in Sydney. But months later Ms Grant, 28, who admits she easily catches colds, is still Covid-free.
'I thought, if anyone is going to get it, it's for sure going to be me. But I didn't. It was super surprising,' she told SBS.
Ms Grant is not alone in being baffled at why she's avoided the much-feared virus. For every story of someone who got sick with Covid-19, there seems to be a parallel tale of someone who expected to fall ill but didn't.
Aside from how Covid-19 started in the first place, why some people don't seem to get sick from it has been one of the greatest mysteries of the pandemic.
Now it is closer to finally being answered for sure, thanks to a ground-breaking Australian research team.
After nearly two and a half years since Covid was first detected, in Wuhan, China, it is now beyond doubt that some people can be exposed but won't get sick - regardless of whether they were vaccinated or not.
In simple terms, the reason some people don't get sick is immunity - either theirs is better or it's just enough to stop them getting sick.
There's also a rare group of people who may be entirely resistant, and a global research project involving three Australian institutions, called the Covid Human Genetic Effort is investigating.
'Although this is not proven yet, there may be individuals completely resistant to the infection itself, as seen with other viruses,' a statement from the project said.
Scientists are in the early stages of finding definite answers to why - because it's only recently apparent that not everyone is going to get Covid-19. The evidence that it's more than just good luck that some people evade Covid-19 is now strong.
Partly that evidence comes from the extraordinary individual cases of people 'hyperexposed' to multiple positive cases, and sometimes caring for them, even without a facemask.
Some of these cases occurred within families where all but one person was sick with the virus, said John Christodoulou from the University of Melbourne, who is involved with the Covid Human Genetic Effort.
'We are collecting information and DNA from individuals who have been ‘hyperexposed’ to Covid but who don’t seem to contract Covid – for example, living in a household where multiple family members were infected, but one member of the household wasn’t – to see if genetic factors can be identified that might offer protection against Covid infection,' said Mr Christodoulou.
Most evidence appears anecdotally from the sheer number of people who have responded to call-outs from researchers wanting to speak to people who never got ill, despite exposure.
Several international studies are underway to answer this question, which researchers ultimately hope will help improve Covid treatment for everyone. And they have received thousands of volunteers eager to help.
Mayana Zatz, a geneticist from the University of São Paulo, went on Brazilian television asking people who had shared a bed with an infected partner but didn't get sick to contact her. She received thousands of emails.
In another study, Imperial College researchers exposed 36 healthy, unvaccinated male and female volunteers (aged between 18 and 30) with a low dose of Covid - but only half became infected.
In other words, coming into contact with Covid-19 and not getting sick - and not even becoming infected - might actually be very common, despite the high case rates
This is not to say that Covid is a hoax, or not as serious as reported.
Just this week the World Health Organisation estimated 15 million people had died from Covid-19 or as a result of the pandemic in the last two years - far more than the officially reported toll of 6.25 million.
Either way that's far more than what Covid is sometimes compared to - influenza, which WHO says kills approximately 650,000 people a year.
The number of people who have fallen sick with Covid is a now a extraordinary 516 million across the globe.
But scientists now accept hundreds of thousands who were obviously exposed did not develop Covid-19.
How did they get that sort immunity? Medics now accept that in some cases, people who did not get sick were just lucky, while others simply had better immunity.
The duration and location of exposure to the virus exposure were vital, as well as how infectious the positive case was - known as their viral load.
But even in situations that people were exposed to someone with a high viral load, they didn't catch it.
The reason some people have better immunity to Covid is believed to be either because of their genes or the way their body responded to a previous virus.
A study by the Imperial College London found that high levels of T cells (a type of white blood cell) created when the body fought off a previous virus - such as the common cold - protects against Covid-19.
'The immune system is good at recognising viruses that aren't exactly the same but come from the same family,' said immunologist Professor Stuart Tangye from the Garvan Institute of Medical Research, 9 newspapers reported.
'Studies from 2020 found that 25-45 per cent of people who were studied and had not previously been infected with SARS-CoV2 had detectable levels of T cells that cross-reacted with SARS-CoV2.'
Melbourne immunologist Vanessa Bryant, who is studying transmission within households, says our immune systems are not all equal. 'Some people might generate an immune response that just makes better antibodies … and we do think this is largely genetic,' said Ms Bryant, of the Immunogenetics Research Laboratory at the Walter and Eliza Hall Institute of Medical Research.
Part of the answer could be in so-called genetic mutations, which can be a good or a bad thing. Professor Tangye said 'genetic influences' can sometimes make people vulnerable to severe illness - or it can improve resistance.
'There are populations of people who probably should have been infected and sick but weren’t,' he said.
Scientists also suspect that genetics could be to blame for young otherwise healthy people developing severe Covid where older, apparently more vulnerable people get less severe symptoms.
'There was clearly a subset - small, rare - but there was a subset of individuals who were otherwise healthy and who developed very serious infections, life-threatening infections.'
He claimed up to five per cent of severe COVID-19 cases in people under 70 could be caused by undiagnosed genetic defects.
Those lucky 'unicorns' who manage to escape infection even at close quarters will be able to sail through the pandemic.
But medics warn against tempting fate and testing your resistance. 'I always encourage people to not go and deliberately get Covid,' added Professor Senanayake.
'Even if they’re young and healthy, they might have some unrecognised risk factor that could give them severe disease.'
https://www.dailymail.co.uk/news/article-10789701/Covid-Australia-people-unicorns-NEVER-Covid.html
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)
http://australian-politics.blogspot.com/ (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com/ (TONGUE-TIED)
https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)
https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)
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6 May, 2022
COVID-19 subvariant XE: What to know
It’s nicknamed Frankenstein, but experts say that shouldn’t scare you.
The World Health Organization (WHO) recently issued a preliminary report on the new COVID-19 "Frankenstein" subvariant called XE, which is a mix of the omicron BA.1 variant and the "stealth" variant BA.2, with the agency declaring it’s still part of the omicron variant, but not a variant of interest or concern yet, according to a recent Euronews report.
The XE strain was first detected in the United Kingdom on January 19, with now over 1,000 cases spreading by community transmission, with the majority in the east of England, London, and South East London, per the report.
A "recombinant" strain is a type of variant that occurs when an individual becomes infected with two or more variants at the same time, and are assigned the letter "X" prefix to classify them as recombinant, said Dr. Stacia Wyman, senior genomics scientist at the Innovative Genomics Institute at UC Berkeley.
Wyman noted the XE subvariant originated from someone who was infected with both the BA.1 and BA.2 variants.
"When the virus was replicating, there was an error and the two viruses combined," she said. "Then the combined virus replicates and is spread to other people."
XE’s genomic sequence is part BA.1 and part BA.2, but the gene that codes for the spike protein that helps the virus attach to healthy cells comes from BA.2. But even though it’s part BA.2, it’s still unknown if previous BA.2 infection will provide immunity to XE, Wyman said.
"Early-day estimates indicate a community growth rate advantage of ~10% [for XE] as compared to BA.2, however this finding requires further confirmation," the WHO said.
But the UK Health Security Agency (UKHSA) noted: "There is currently insufficient evidence to draw conclusions about growth advantage or other properties of this variant," according to a March 25 updated release.
People are testing positive for 10 days or more when they are diagnosed with the XE variant, said Denis Kinane, immunologist and founding scientist of United Kingdom-based Cignpost Diagnostics.
"Our current data is showing that many people are testing positive for 10 days or more rather than the 6 or 7 days we saw by frequent testing at the beginning of the omicron wave, which means the virus has more opportunity to spread more widely and this may be BA-2 and XE’s transmissibility advantage," Kinane said.
At least two XE cases have been sequenced in Wisconsin and one in New York with also two unconfirmed cases in California, according to Wyman. Japan, China, Thailand, India, New Zealand, and Israel have reported COVID-19 cases secondary to the XE subvariant, in addition to the U.K.
"We continue to monitor cases of the recombinant XE variant in the U.K., which currently represents a very small proportion of cases," said Meera Chand, director of clinical and emerging infections at UKHSA.
"Recombinant variants are not unusual, particularly when there are multiple variants in circulation - and several have already been identified over the course of the pandemic," said Dr. George Thompson, professor of medicine at the University of California, Davis, School of Medicine in the Division of Infectious Diseases.
Thompson told Fox News: "It may be slightly more transmissible than the parent variant but it is too early to known if outcomes differ from other COVID variants."
"As with other kinds of variant[s], most will die off relatively quickly," said Susan Hopkins, chief medical advisor of UKHSA.
Because viruses naturally mutate over time, recombinant strains are not surprising, so presently XE does not appear to be more effective at evading immunity from previous vaccination or prior COVID-19 infection compared with the previous strains, said Dr. Carlos Malvestutto, an infectious disease specialist at the Ohio State University Wexner Medical Center.
But Hopkins noted, "So far there is not enough evidence to draw conclusions about transmissibility, severity or vaccine effectiveness."
Some experts argue, however, because XE is a combined strain of both BA.1 and BA.2 and vaccination protects against symptomatic disease for BA.1 and BA.2 strains, it is likely vaccination will also protect against symptomatic disease caused by XE, said Dr. Andrew Badley, professor of infectious disease at the Mayo Clinic and chair of the COVID-19 Task Force for Mayo Clinic.
The most common symptoms reported of the XE strain are similar to the cold-like symptoms of original strain of omicron – especially in vaccinated people, like runny noses, sore throats and sneezing in contrast to the original strain of the virus that causes COVID-19, like fevers, cough or loss of taste or smell, according to the Independent.
Badley added: "We also know that the other therapies that are being used particularly in the outpatient setting—Paxlovid and molnupiravir—should, based on how they work, have continued activity against the XE strain."
But Badley noted because some monoclonal antibody therapies are not effective against BA.1 and BA.2, it is likely those specific antibody treatments won’t work against XE either.
"The key takeaway is that for each of these variants and subvariants, risk of hospitalization and death appears to be, on average, lower where vaccination rates are higher, indicating that vaccination, including a third dose, should be effective in reducing risk for severe disease," said Stephanie Silvera, professor of public health at Montclair State University.
Approximately 62% of all COVID-19 cases in the United States are currently BA.2, but a new BA.2 subvariant, BA.2.12.1, is now responsible for 36.5% of new coronavirus infections, according to recent data from the Centers for Disease Control and Prevention (CDC).
"We're just starting to learn about the impact of BA.2.12.1," CDC Director Rochelle Walensky said.
"It appears it might have a transmission advantage of about 25% over the BA.2 subvariant. … But importantly, we continue to believe that those who are vaccinated and especially those who are boosted, continue to have strong protection against severe disease, even from BA.2.12.1."
Wyman added the XE recombinant strain "may die out completely regionally and never spread."
"It’s something to keep an eye on, but not for the general population to worry about."
https://www.foxnews.com/health/covid-19-subvariant-xe-ba-2-coronavirus-pandemic
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FDA puts new limits on Johnson & Johnson vaccine due to rare blood clotting condition
The FDA revised its emergency authorization to sharply limit the use of Johnson & Johnson's COVID-19 vaccine due to a rare but potentially fatal blood clotting condition called thrombosis with thrombocytopenia syndrome (TTS).
Only individuals who are 18 years of age and older who "would otherwise not receive a COVID-19 vaccine" due to availability or their choice should now take Johnson & Johnson's one-shot regiment.
"Our action reflects our updated analysis of the risk of TTS following administration of this vaccine and limits the use of the vaccine to certain individuals," Dr. Peter Marks, the director of the FDA’s Center for Biologics Evaluation and Research, said in a statement Thursday.
COVID vaccine Johnson & Johnson
Syringes filled with the Johnson & Johnson vaccine are shown, Thursday, May 13, 2021, at a mobile vaccination site at the Greater Bethel Church in Miami. (AP Photo/Wilfredo Lee / AP Newsroom)
"We’ve been closely monitoring the Janssen COVID-19 Vaccine and occurrence of TTS following its administration and have used updated information from our safety surveillance systems to revise the EUA," Marks added.
The CDC's Advisory Committee on Immunization Practices unanimously voted in December to give a preferential recommendation to Pfizer and Moderna's two-shot mRNA vaccines.
TTS is a syndrome of blood clotting in combination with low levels of platelets, which are the blood cells that help your body halt bleeding.
Health officials have confirmed 60 cases of TTS following Johnson & Johnson's vaccine, nine of which have been fatal.
Women between the ages of 30 and 49 are most vulnerable to the blood clotting disorder, according to the CDC.
About 18.7 million doses of Johnson & Johnson's vaccine have been administered in the United States.
https://www.foxbusiness.com/economy/fda-puts-new-limits-johnson-johnson-vaccine-rare-blood-clotting
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Nearly 15M deaths worldwide associated with COVID-19: WHO
The World Health Organization (WHO) said Thursday that its new estimates show the full death toll associated directly or indirectly with the COVID-19 pandemic between Jan. 1, 2020, and Dec. 2021 was approximately 14.9 million.
Scientists said there were between 13.3 million and 16.6 million deaths either caused directly by the coronavirus or attributed to the pandemic’s impact on health systems during that time.
That number is more than double Johns Hopkins University's official death toll of more than 6 million, with the majority of excess mortality – calculated as the difference between the number of deaths that have occurred and the number that would be expected in the absence of the pandemic based on previous data – in Southeast Asia, Europe and the Americas.
"Most of the excess deaths (84%) are concentrated in South-East Asia, Europe and the Americas. Some 68% of excess deaths are concentrated in just 10 countries globally. Middle-income countries account for 81% of the 14.9 million excess deaths (53% in lower-middle-income countries and 28% in upper-middle-income countries) over the 24-month period, with high-income and low-income countries each accounting for 15% and 4%, respectively," the agency said.
A team led by Canadian researchers estimated that there were more than 3 million uncounted coronavirus deaths in India alone, whereas WHO's new analysis estimated that missed deaths in India ranged between 3.3 million to 6.5 million.
Disputing the WHO's methodology, India's Health and Family Welfare Ministry labeled the analysis as "questionable," complaining that the estimates were released "without adequately addressing India's concerns."
The estimates for the two-year period confirm that the global death toll was higher for men than for women and higher among older adults.
The estimates are the result of a global collaboration supported by the work of the Technical Advisory Group for COVID-19 Mortality Assessment and country consultations.
While many countries still lack the capacity for reliable mortality surveillance, using publicly available methodology the WHO says countries can use their own data to generate or update their estimates.
"These sobering data not only point to the impact of the pandemic but also to the need for all countries to invest in more resilient health systems that can sustain essential health services during crises, including stronger health information systems," WHO director-general Dr. Tedros Adhanom Ghebreyesus, said in a statement. "WHO is committed to working with all countries to strengthen their health information systems to generate better data for better decisions and better outcomes."
The WHO said it wasn't yet able to distinguish between direct deaths from COVID-19 and others caused by the pandemic nothing that a future project examining death certificates would probe this.
https://www.foxnews.com/health/who-global-deaths-covid-reach-nearly-15-million
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)
http://australian-politics.blogspot.com/ (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com/ (TONGUE-TIED)
https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)
https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)
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5 May, 2022
Why the Feds Are Clinging to Their Mask Mandate
Bureaucrats cling to power. It’s their institutional predisposition.
So it was no surprise on Wednesday when the Department of Justice appealed the recent Federal court ruling that struck down the mask mandate imposed on mass transportation by the Centers for Disease Control.
As the appeal demonstrates, governments are especially reluctant to give up emergency powers. When they do, the relinquishment is grudging and only partial.
That is a big reason why big government keeps getting bigger. As economist Robert Higgs showed in his book Crisis and Leviathan, since the early 20th century, the US government has exploited every national emergency to seize emergency powers.
After the crisis subsides, government power recedes, but never all the way back to pre-crisis levels. In this way, the federal government “ratchets up” its power, at the expense of our liberty, crisis after crisis.
This “ratchet effect,” as Higgs termed it, is on vivid display in airports especially. There, the travel mask mandate persisted long after the pandemic panic subsided and many other COVID policies were rolled back. And if the DOJ’s appeal succeeds, it may return and linger even longer.
The wretched ratchet effect is also manifest in the many post-9/11 airport security policies that the Transportation Security Administration continues to enforce more than two decades after the crisis that spawned them.
A curious aspect of many of these policies is how seemingly petty they are. Why is the government so adamant about travelers removing their shoes at security and wearing masks? The effectiveness of such measures has been shown to be highly dubious at best. Moreover, such compelled performances of “security theater” and “hygiene theater” don’t even seem to provide much material benefit to the government. What’s the point of ratcheting up that kind of power?
I suspect a major purpose of such petty policies is the mass inculcation of obedience. Security theater and hygiene theater are part and parcel of a broader “obedience theater.” Humiliating compulsory gestures like removing your shoes and wearing your mask are obeisances: symbolic ritual acts of self-abasement and submission.
It’s not about keeping you safe or healthy. It’s about showing you who’s boss.
https://catalyst.independent.org/2022/04/22/feds-mask-mandate/
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COVID-19 Vaccine Can Trigger Acute Hepatitis
A recent case report about a man who received an mRNA-based COVID-19 vaccine suggests that taking the vaccine “may trigger immune-mediated hepatitis,” researchers wrote.
The case report does not indicate how common such a case would be, although researchers said that such a scenario is recognized as a “rare adverse event not identified in early trials.”
The report, published in the Journal of Hepatology in late April, describes the case of a man in Germany aged 52 who developed acute hepatitis—liver inflammation—two to three weeks after having received an mRNA-based COVID-19 vaccine from Pfizer-BioNTech (the BNT163b2 vaccine).
Researchers said they found that highly-activated T cells “accumulate and are evenly distributed in the different areas” of the man’s liver after he took the COVID-19 vaccine and developed acute hepatitis. T cells are a type of white blood cell that comprise a key part of the immune system. These cells focus on fighting new infections.
The patient experienced nausea and fatigue about 10 days after his first dose of the vaccine, and was subsequently found to have acute hepatitis. The hepatitis resolved on its own after about three days. He had a second dose of the vaccine 41 days after his first dose. Symptoms of nausea and fatigue returned 20 days later—he was given an oral steroid medication and initially improved. He relapsed 39 days later, after which he was successfully treated with systemic immunosuppressive therapy that also included steroids. The man’s liver function tests “subsequently normalized within 8 weeks.”
Researchers said the man’s immune response to the COVID-19 vaccine may have contributed to his liver inflammation. The COVID-19 vaccine from Pfizer “may trigger immune-mediated hepatitis by mechanisms linked to vaccine-induced cellular immunity,” they said in the case report.
Within the T cells that were found in the liver, the scientists observed “an enrichment of T cells that are reactive to SARS-CoV-2, suggesting that these vaccine-induced cells can contribute to the liver inflammation in this context.”
Specifically, the type of T cell called CD8 T cells “represented the most abundant immune cell subset” found in the liver. “Our analysis highlights that activated cytotoxic CD8 T cells including vaccine-induced spike-specific CD8 T cells could contribute to disease pathogenesis,” researchers wrote.
“Based on their strong enrichment … we speculated that CD8 T cells could be drivers of the hepatic inflammation.”
The authors called the case one that appears to be autoimmune hepatitis, but is not. “Autoimmune-hepatitis-like disease after vaccination against SARS-CoV-2 is now recognized as a rare adverse event not identified in early trials,” they wrote. “The widespread use of the vaccine with administration of hundreds of million doses worldwide raises also questions of causality vs. coincidence.”
The authors wrote it is important to differentiate autoimmune hepatitis from hepatitis triggered by immune responses after COVID-19 vaccination; the former requires lifelong immunosuppressive therapy in many patients, while the latter is possibly transient, they noted.
https://www.theepochtimes.com/covid-19-vaccine-can-trigger-acute-hepatitis-case-report_4442123.html
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Tearing Down the Silicon Valley Wall
Elon Musk has finally managed to buy Twitter. And the moment he did, the enraged left flipped out.
Abruptly, leftists began trashing their favorite electronic communications platform as the domain of the nation’s elite, professional classes. Had they just discovered that they had been racists and privileged users all this time?
And what happened to the left’s former worship of Musk as the man who revolutionized the clean, green automobile industry with his Tesla electric car company?
Or Musk, the space revolutionary and hip star trekker, who with his own money helped ensure the United States remains preeminent in space exploration?
Or Musk, the patriot who is providing free next-generation internet service to the underdog Ukrainians fighting Russians for their lives?
No matter. The left reviles Musk because he has announced that Twitter will be the one social media platform whose business is not to censor or massage free speech in an otherwise monopolist, intolerant, and hard-left Silicon Valley.
Who knows, Musk might even allow former President Donald Trump to communicate on Twitter—in the fashion that the terrorist Taliban, Iranian theocrats, and violent Antifa protesters all take for granted in their daily access to Twitter.
But how did the once free speech, anti-trust, “let it all hang out” left become a Victorian busybody, a censorious Soviet, and an old-fashioned robber-baron monopoly?
When it discovered that few Americans wanted left-wing, socialist politics it turned elsewhere. It found power instead through control of American institutions, from academia and Wall Street to traditional and social media.
When Musk merely talked about buying Twitter, the left shrieked that an outlier multibillionaire owning a media—and especially a social media—venue was unfair. The buyout was supposedly “dangerous” and “a threat to democracy.”
But the more the left screamed, the less people listened.
After all, left-wing Mark Zuckerberg’s Facebook has roughly 15 times more market capitalization than Twitter. It has an audience of 2 billion users—over seven times larger than Twitter’s 271 million.
Zuckerberg’s monopoly on global social media and his enormous wealth were stealthily put in service to the Democratic Party in the 2020 election. He reportedly infused nearly $420 million of his media money into warping the vote in key precincts, by augmenting and absorbing the work of state registrars to empower likely left-wing voters.
Amazon’s Jeff Bezos, the second wealthiest man in the world, owns the influential Washington Post. It has moved markedly to the activist left under his patronage.
Multibillionaire Lisa Jobs, widow of the late Apple founder Steve Jobs, owns The Atlantic. It has become an increasingly hard-left political magazine.
So in Orwellian fashion, apparently most media-owning, left-wing billionaires are good? But one social media-owning, non-left-wing billionaire is bad?
How exactly might a Musk-owned Twitter alter an election?
By emulating the former directors of Twitter and the rest of Silicon Valley social media who canceled not just conservatives, but any new communication they felt harmful to the 2020 Biden campaign?
From the outset, it was clear that Hunter Biden’s lost laptop incriminated his dad, Democratic nominee Joe Biden.
Biden was referenced by his own quid pro quo, grifting son variously as “the Big Guy” and “Mr. Ten Percent”—a full partner in peddling Beltway influence to rich foreign actors.
Yet in lockstep, social media banned most coverage of the pre-election laptop story.
It instead spread its standby false narrative of “Russian disinformation.” We now know the laptop was always authentic. The crude efforts to suppress mention of it were classic politicized news suppression.
Still, the left may well have some reason to be terrified of Musk. Should he liberate Twitter from left-wing scolds and groupthinkers, would other renegade new companies and old standbys follow his lead?
Is Musk’s $46 billion acquisition the internet equivalent of Germans in November 1989 with sledgehammers smashing down the Berlin Wall?
Does Musk sense that the looming November midterm elections may result in one of the rare landslide verdicts in American history?
Does he assume the public prefers a muckraker who demands free speech rather than corporate insider cronies censoring expression they don’t find useful?
Polls show that the American people have had their fill of 14 months of self-inflicted, ideology-driven disasters. And why not, given the nonexistent border, spiking crime, inflation, unaffordable gasoline, and neo-Confederate racial fixations?
Are the recent Netflix implosion, the CNN+ disaster, the Disney debacle, the Virginia statewide and San Francisco school board elections, the polls showing massive defections of Latinos from the left, the grassroots pushback against government-imposed mask wearing, and explicit transgender education in the k-3 grades also symptoms of a reckoning on the horizon?
The country is ready for a revolution. And Musk believes he can lead it with his Silicon Valley sledgehammer. So, as the left says, “Bring it on.”
https://www.dailysignal.com/2022/04/28/tearing-down-the-silicon-valley-wall/
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)
http://australian-politics.blogspot.com/ (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com/ (TONGUE-TIED)
https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)
https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)
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4 May, 2022
Double-masking DOESN'T work and might raise risk of catching and spreading Covid, study finds — despite US health chiefs STILL recommending it
Double-masking does not stop people from catching or spreading Covid — and it might even raise their risk, a study suggests.
US health chiefs have been advising Americans to double-up if they can't get their hands on a medical-grade mask since early 2021, claiming it increases protection.
But now researchers say wearing two masks may actually do the opposite, by creating 'a false sense of security' that causes people to take unnecessary risk.
Wearing two cloth masks can also force more air through the gaps between the face, increasing the amount of virus breathed into the air, they found.
The study, which used computer simulation models, looked at cloth masks so the findings do not necessarily apply to surgical masks or N95s used in hospitals.
However, the researchers noted that wearing two tight-fitting masks could cause 'breathing difficulties'.
The Centers for Disease Control and Prevention (CDC) recommends wearing a cloth mask on top of a surgical mask to achieve a 'better fit and extra protection'.
Experts from Florida State University and Johns Hopkins University made computer simulations of 3D heads based on 100 men and 100 women.
The researchers simulated a cough jet from the mouth of the models, which wore a cloth mask over the nose and mouth and elastic hoops wrapped around the ears.
The team calculated the filtration efficiency, which measures how much virus-filled droplets are captured or blocked by the mask.
The findings, published in the journal Physics of Fluids, show wearing two face coverings provide 'negligible, if any, increase in protection'.
However, they said while it could 'theoretically' reduce the amount of virus that could pass through the mask, if two good-fitting face coverings are worn, it 'could also lead to breathing difficulties'.
A second poor-fitting masks decreases the amount of air that can be filtered through the covering — forcing more air through any gaps between the mask and face.
They said people could also have a 'false sense of security when choosing to double mask', and therefore be less likely to social distance or take other precautions.
Double masking has become 'more and more popular' for Americans who cannot access the most effective N95 and KN95 masks, the researchers said, which makes the findings important.
They said one cloth mask would be better than two, but the best type of mask is one that fits tightly like an N95 or KN95. UK health chiefs have previously said there is 'insufficient evidence' to recommend double-masking.
Covid is mainly spread through droplets an infected person releases when they breathe, speak, cough or sneeze. Large particles can land in the nose or mouth of people nearby, while smaller airborne droplets stay suspended in the air can be breathed in.
Evidence shows that, when worn correctly, masks can reduce the spread of these particles — but by how much is still contested.
https://www.dailymail.co.uk/health/article-10777965/Double-masking-DOESNT-work-raise-risk-catching-spreading-Covid.html
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Trump’s Truth Social platform could help propel GOP to majorities in the 2022 midterms and beyond
No risk, no reward. That’s the lesson official Washington, D.C. should now be learning from former President Donald Trump’s foray into running a social media company, TruthSocial.com, which is currently running a successful public beta that Apple customers can download in the App Store.
Before the app has even been offered on other platforms such as Android or via desktop computers, President Trump has already garnered almost 2.4 million followers — in a week — as the app rocketed to the top of the App Store as the most downloaded app the past several days.
Before he was banned by Twitter and Facebook in 2021, Trump had more than 80 million followers, and while he is still quite a ways off from where he was, he and the team at Truth Social including CEO Devin Nunes have to be very pleased with the current rollout so far.
And here’s why.
Anecdotally, we can tell you that so far the Americans for Limited Government’s @LimitGov profile is seeing significant engagement that appears vastly superior to other social media platforms such as Twitter or Facebook despite smaller initial subscription counts.
To be fair, ALG’s cartoonist A.F. Branco and Truth Social CEO Devin Nunes, did each give us generous boosts on the platform. That will get you follows, but that doesn’t necessarily mean those followers will engage with your content. In this case, thankfully, they are engaging.
We can see the difference compared to other platforms. And Truth Social wants us to grow.
In other words, there might be fewer people on the Truth Social platform so far compared to some of the other more established platforms, but the ones that are on Truth Social already are not merely engaging with posts, they’re actually clicking off of the platform to the offsite content that is being shared at a much, much higher conversion rate.
Now, how that holds up over time is another question, but Trump seems to be onto something here, especially if one plans on being politically active on the platform. So far, Truth Social appears to be attracting, at least initially, a primarily conservative, Republican audience whose users also happen to be very strong supporters of Trump and are very civic-minded.
These are likely voters. By appearing exclusively on Truth Social, Trump is driving engagement — and giving Republicans in the midterms a reason to log in.
In the midterms, enthusiasm always comes into play, where the opposition party tends to generate more of it than the incumbent party. In midterm elections dating back to 1906 through 2018, the party that occupies the White House usually loses on average 31 seats in the House, and about three seats in the Senate. That’s more than enough for Republicans to take back one or both chambers of Congress in 2022.
On that count, presently in the latest ABC News/Washington Post poll conducted April 24-28 of registered voters, 83 percent of Republicans report they are absolutely certain to vote in November, compared to 76 percent of Democrats, giving Republicans a 7-point edge.
More broadly, Republicans are leading the generic ballot by on average 4.2 points, 46.4 percent to 42.2 percent, according to RealClearPolitcs.com.
These are all readings one would expect to see in a midterm cycle with a Democratic President and Republicans out of power.
That is why Truth Social is almost certainly the place where Republican members and candidates for Congress are going to want to gravitate towards in 2022 for the November midterms. What better way to build a fresh list of supporters on a platform that is finally not controlled by Silicon Valley? This could be a game-changer.
Here, Trump has figured out a way to capture the energy Republicans are gaining through the midterms, by giving conservative activists a platform that gives them the information they want, and causes like Americans for Limited Government they can support wholeheartedly.
This is an opportunity for the conservative movement to grow.
And Trump is getting every single one of their email addresses with every single download from the App Store, who can now follow him every day. They won’t all be his supporters, but here, Trump has created a product that grants exclusive access to his thoughts and ideas, whether they are about what direction the country should be headed in, criticizing President Joe Biden or if he is endorsing candidates on the campaign trail.
Trump is helping the GOP to build a wider platform in 2022, and if he chooses to run for president again, in 2024. How many other Republican candidates will have a social media app to help them win the Republican primary or general election in 2024? How many would have even tried to stand up to Big Tech’s tyranny in this way?
In modern politics, this is not only how to build a movement, but an institution
https://dailytorch.com/2022/05/trumps-truth-social-platform-could-help-propel-gop-to-majorities-in-the-2022-midterms-and-beyond/
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)
http://australian-politics.blogspot.com/ (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com/ (TONGUE-TIED)
https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)
https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)
https://westpsychol.blogspot.com/ (The Psychologist -- backup)
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3 May, 2022
Did vaccination make things worse?
Jean Curthoys
For almost two years, it has been an article of faith that the only way out of this Covid pandemic is mass vaccination.
On the surface, this has looked to be a plausible claim. It has been repeatedly and forcefully endorsed by public health officials and medical experts. Most people have been happy to go along with it, if not positively embrace it. Unsurprisingly, the result was the creation of an unvaccinated minority who have been subjected to accusations of selfishness, ‘anti-scientism’, and ostracised from society to varying degrees.
As one blogger put it, the unvaccinated ‘have cooties’.
The unvaccinated, in turn, haven’t held back from judging those who have judged them. They are genuinely bewildered as to how erstwhile sceptics of both Big Pharma and government integrity have been so eager to be injected with the former’s rushed product on the say-so of the latter. This led the unvaccinated to parody their accusers as sheep (‘sheeple’), blindly following authority to the Orwellian stage where they hold two contradictory beliefs: the vaccines are ‘safe and effective’ and the unvaccinated pose a life and death risk to the vaccinated.
Dr Robert M. Rennebohm is a retired paediatrician who wants to help with this unhappy situation that is straining, if not destroying, friendships and families.
He believes he can do this by passing on the clarity he achieved by spending the last two years deepening his understanding of the complexities of the human immune system. To this end, he has released An Open Letter to Parents and Paediatricians Regarding Covid Vaccination, which has been received as a masterpiece exposition of a highly complex subject. While the letter itself is 121 pages, the 10-page summary provides substantial illumination of the issues at stake and requires no more than an hour or so of focused attention. You can also listen to Rennebohm interviewed here.
As Rennebohm sees it – leaving aside the overwhelming media support for the official narrative – one reason for the impasse between supporters and opponents of Covid vaccine policy is that it depends on scientific questions which are beyond most of us. Consequently, those who accept vaccine mandates usually do so on the basis of authority, while those who reject them argue from a fundamental human rights framework along with the general risks of a product without the usual ten-year safety profile.
The two sides are talking past each other, both failing to address the core issue.
The core issue is whether mass vaccination was (and is) the ‘only way’ out of the pandemic. It is a fundamental question because the extent to which mass vaccination is for the greater good is the extent to which there is a case for weakening human rights and accepting the risks of vaccination. But this is a question of virology and immunology that can’t be addressed without a basic grasp of the relevant science. Rennebohm’s ‘Open Letter’ enables this bridge to be crossed by comparing the scientific support for the official policy with that for a significant dissenting view.
This is where things could become confronting for adherents to the mainstream, as they did for Rennebohm himself when he delved more deeply into the science.
The counter-narrative he examines in his letter has been advanced by the virologist Geert Vanden Bossche, well known to those who venture down the ‘rabbit hole’ of alternative media, but referred to in the mainstream media only as ‘misinformation’. Vanden Bossche’s thesis – argued with some passion – is that mass vaccination with imperfect vaccines (the only ones we have for respiratory viruses of this nature) and undertaken in the middle of a pandemic has been, and will continue to be, disastrous. The strategy is counterproductive, both for individuals and for the course of the pandemic – for individuals because it erodes natural immunity, and for the evolution of the pandemic because it enables the continual selection of variants that escape the vaccine. Moreover, the two factors compound each other. Mass vaccination, he maintains, makes the situation immeasurably worse.
This is a confronting idea if Vanden Bossche is right. As laid out by Rennebohm, the science suggests that he could be. More accurately, his argument has scientific support despite the prevailing narrative.
The implication is clear. Far from the world having experienced a pandemic of the unvaccinated, the reverse is the case – the pandemic has been prolonged by mass vaccination, and the overall health of the population would have been better served had a significant majority remained unvaccinated. The demonisation of the unvaccinated as socially irresponsible has no scientific basis.
While the experience of the last two years largely supports Vanden Bossche’s analysis, his work and that of others who argue to a similar conclusion, will remain unaddressed because the official policy is defended on the unverifiable ground that things ‘would have been much worse’ had it not been pursued. In this context, Rennebohm’s role is simply that of bringing Vanden Bossche’s work to the attention of the public.
The objective of Rennebohm’s exercise in basic science education is not to train citizen scientists, but to put some genuine and accessible information into the ‘informed consent’ theoretically required of the vaccinated. For the unvaccinated, his ‘Open Letter’ provides vindication. The wider hope is for some kind of reconciliation for those whose friendships and family relationships have been soured or disrupted.
https://www.spectator.com.au/2022/05/did-we-make-things-worse/
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New Omicron variants can dodge infection antibodies but jabs helps, study suggests
New Omicron sublineages show an ability to evade antibodies from earlier infection, a new Covid study has found.
But the deadly virus is far less able to thrive in the blood of people vaccinated.
Experts at a South African laboratory believe it could signal a fresh wave of infections in the country in the months ahead as with only 30 per cent of the popular fully jabbed.
Blood samples from people who had been infected with the original Omicron variant saw a big drop in neutralising antibody production when tested against the BA.4 and BA.5 sublineages that were discovered this month in South Africa.
“The low absolute neutralisation levels for BA.4 and BA.5, particularly in the unvaccinated group, are unlikely to protect well against symptomatic infection,” the researchers said.
“This may indicate that, based on neutralisation escape, BA.4 and BA.5 have potential to result in a new infection wave.”
On Saturday South Africa recorded 6,527 new cases and a test positivity rate of 21.5%.
The scientists from multiple institutions were examining Omicron's BA.4 and BA.5 sublineages, which the World Health Organisation recently added to its monitoring list.
They took blood samples from 39 participants previously infected by Omicron when it first showed up at the end of last year.
Fifteen were vaccinated - eight with Pfizer's shots, seven with Johnson & Johnson’s - while the other 24 were not.
"The vaccinated group showed about a 5-fold higher neutralisation capacity, and should be better protected," they added.
In the unvaccinated samples, there was an almost eightfold decrease in antibody production when exposed to BA.4 and BA.5, compared with the original BA.1 Omicron lineage.
South Africa may be entering a fifth Covid wave earlier than expected, officials and scientists announced on Friday.
They are blaming a "sustained" rise in infections that seems to be driven by the BA.4 and BA.5 Omicron sub-variants.
Only about 30% of South Africa's population of 60 million is fully vaccinated.
https://theworldnews.net/gb-news/new-omicron-variants-can-dodge-infection-antibodies-but-jabs-helps-study-suggests
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)
http://australian-politics.blogspot.com/ (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com/ (TONGUE-TIED)
https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)
https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)
https://westpsychol.blogspot.com/ (The Psychologist -- backup)
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2 May, 2022
‘What I’ve Seen in the Last 2 Years Is Unprecedented’
Dr. James Thorp is an extensively published 68-year-old physician MD board-certified in obstetrics and gynecology, as well as maternal-fetal medicine, who has practiced obstetrics for over 42 years.
Thorp told The Epoch Times that he sees 6,000–7,000 high-risk pregnant patients a year and has seen many complications among them due to the COVID vaccines.
“I’ve seen many, many, many complications in pregnant women, in moms and in fetuses, in children, offspring,” Thorp said, “fetal death, miscarriage, death of the fetus inside the mom.
“What I’ve seen in the last two years is unprecedented,” Thorp asserted.
Thorp explained that although he has seen an increase in fetal death and adverse pregnancy outcomes associated with the COVID-19 vaccination, attempts to quantify this effect are hampered by the imposition of gag orders on physicians and nurses that were imposed in September 2021, as reviewed in the publication “Patient Betrayal: The Corruption of Healthcare, Informed Consent and the Physician-Patient Relationship” (pdf).
At the beginning of January, the FDA was ordered to release its first large batch of documents related to Pfizer’s COVID jab trials, of which over 10,000 of about 450,000 pages have been made public so far.
From the first day of the Pfizer-BioNTech vaccine rollout on Dec. 1 2020 through Feb. 28, 2021, 1,223 deaths and 42,086 adverse events were reported to Pfizer.
Among the adverse events, particularly alarming are the ones that affected pregnant women. The documents say that there were 274 pregnancy adverse events, of which 75, or 27 percent were “serious.”
“49 non-serious and 75 serious, reported clinical events, which occurred in the vaccinated mothers. Pregnancy related events reported in these cases coded to the [patients] Abortion spontaneous (25), Uterine contraction during pregnancy, Premature rupture of membranes, Abortion, Abortion missed, and Foetal death (1 each). Other clinical events which occurred in more than 5 cases coded to the [patients] Headache (33), Vaccination site pain (24), Pain in extremity and Fatigue (22 each), Myalgia and Pyrexia (16 each), Chills (13) Nausea (12), Pain (11), Arthralgia (9), Lymphadenopathy and Drug ineffective (7 each), Chest pain, Dizziness and Asthenia (6 each), Malaise and COVID-19 (5 each),” reads the previously confidential Pfizer documents (pdf).
The CDC website recommends the COVID vaccines during pregnancy in order to “prevent severe illness and death in pregnant women.”
The American College of Obstetricians and Gynecologists (ACOG) also “strongly recommends that pregnant individuals be vaccinated against COVID-19,” adding that pregnant women’s complete vaccination should be a “priority.”
Thorp repeatedly emphasized that it’s not that everybody got their shots when the vaccine was first distributed.
“They were not all administered [on Dec 1, 2020,]” Thorp said. “All the lots that were sent out were deep-frozen on-site and then they were administered slowly over that eight weeks.”
The amount of BioNTech vaccines shipped worldwide at the time has been redacted in the aforementioned document.
“Why did they redact that? That would have been unbelievable information that would give you the exact numerator and denominator,” Thorp said.
The “general overview” table says that there were 29,914 “cases” related to females, 9,182 in males, and 2,990 people with “no data,” of which 19,582 are “recovered/recovering,” 11,361 “not recovered at the time of the report” and 1,223 “fatal.”
Former Pfizer VP Had Given Warnings
Michael Yeadon is a big pharma veteran with 32 years in the industry. He retired from Pfizer whilst occupying the most senior research position in that field.
“On December 1, 2020, We detailed a series of mechanistic toxicology concerns which we believed were reasonable to hold, unless & until proven not to occur,” Yeadon said in a statement to The Epoch Times.
“Among those was that adverse impacts on conception and ability to sustain a pregnancy were foreseeable.”
“It’s important to note that none of these gene-based agents had completed what’s called ‘reproductive toxicology.’ Over a year later, this battery of tests in animals still has not been done. So there was and still is no data package supporting safety in pregnancy or prior to conception.”
Dr. Wolfgang Wodarg and Yeadon detailed the concerns on the issue: the spike protein from the virus encoded in the vaccines was related to a minor extent to syncytin that plays a crucial part in the carrying of a baby to term.
Yeadon had hoped, back then, that their concerns were paid attention to, since they had already seen the tragedy of thalidomide, a sedative drug that caused congenital malformation, over 60 years ago.
“During 2021, I came across two further pieces of evidence which made it much more likely that there’d be adverse effects on pregnancy from COVID-19 ‘vaccines.'”
“It looked like someone had tried to dismiss our concerns by testing for evidence of the particular problem we’d warned about in Dec. 2020. Unfortunately, all they did is to reinforce our concerns. We’d envisioned the risk that, in responding to the synthetic piece of virus spike protein, women’s immune systems would also make an immune response to their own placental protein,” Yeadon said. “That’s exactly what was reported in the pre-print paper.”
“Based on this concern alone, all of these experimental products as a class should have been completely contraindicated in women younger than menopause.”
mRNA Products Accumulate in Ovaries
Another concern that they had not initially noticed was that “the mRNA products (Pfizer & Moderna) would accumulate in ovaries,” Yeadon stated.
“An FOI request to the Japanese Medicines Agency revealed that product accumulation in ovaries occurred in experiments in rodents. I searched the literature based on these specific concerns and found a 2012 review, explicitly drawing attention to the evidence that the lipid nanoparticle formulations as a class do, in fact, accumulate in ovaries and may represent an unappreciated reproductive risk to humans. This was ‘a well known problem’ to experts in that field.”
A 2012 study says that after testing with different mouse species and Wistar rats, “a high local accumulation of nanoparticles, nanocapsules and nanoemulsions in specific locations of the ovaries was found in all animals.”
Referring to the study, Yeadon told The Epoch Times that “The authors tell untruths. They say something like ‘there was no increase in anti-syncytin-1 antibodies.'”
“No, that’s wrong. Their data is clearly 2.5X increased after vaccination & obviously statistically significant (Functional significance is looking confirmed by the miscarriage rate,)” Yeadon noted.
“What they’re done is cute. They’ve chosen a completely arbitrary level they scribed on the figure below which they claim nothing matters. No evidence whatsoever for that claim. In fact, in the discussion, they confess we don’t know the relationship between antibodies & impact on function.”
The former Pfizer VP believes that the pharmaceutical industry “definitely knew,” since 2012, that the lipid nanoparticles would accumulate in the ovaries of women that took the vaccines.
“No one in the industry or in leading media could claim ‘they didn’t know about these risks to successful pregnancy.'”
A lipid nanoparticle is an extremely small particle, it’s a fat-soluble membrane that is the cargo of the messenger RNA, Thorp said.
“From data that we have, there appears to be a concentration of the lipid nanoparticles, which are very, very small particles, which are in the vaccine that are injected into the arm,” Thorp said, “and then the vast majority of those are dispersed throughout the entire body.”
“They appear to concentrate in the ovaries, and they appear to cross all God-made barriers in the human body, the blood-brain barrier, the placental barrier during pregnancy, into the fetal bloodstream, and all the fetal tissues inside the womb, crossing the blood-brain barrier in the fetus, the baby in the womb, which is very concerning,” he noted, since the eggs produced by women are limited in number, and they would be “exposed to a potentially disastrous toxic lipid nanoparticle.”
Dr. Christiane Northrup is a board-certified obstetrician-gynecologist with more than 30 years of experience and the former president of the American Holistic Medical Association. She also served on their board during the 80s and early 90s.
She told The Epoch Times last October about how were women being affected by the vaccines.
“Women are having bleedings. The doctors in our area are doing hysterectomies in young women, like 30-somethings, they said, ‘Oh, it’s not unusual.’ Let me tell you, as a board-certified gynecologist, that’s very unusual. Women’s periods are messed up all over the place … I’ve had a huge Facebook group of thousands of women talking about this situation that was removed,” Northrup said.
“My profession is famous for embracing treatments that later on turn into disasters: For example the drug thalidomide that results in limb effects in hundreds of babies, the Dalkon shield IUD that was touted as the birth control method of choice for women who had never had children—and then made hundred of them sterile from infection. And of course, there is DES (diethylstilbestrol) that was given to thousands of women for nausea of pregnancy—and results in reproductive abnormalities in both male and female offspring—including sterility,” Northrup added on Tuesday.
Pfizer and Moderna did not respond to requests for comment.
https://www.theepochtimes.com/what-ive-seen-in-the-last-two-years-is-unprecedented-physician-on-covid-vaccine-side-effects-on-pregnant-women_4428291.html
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)
http://australian-politics.blogspot.com/ (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com/ (TONGUE-TIED)
https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)
https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)
https://westpsychol.blogspot.com/ (The Psychologist -- backup)
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1 May, 2022
Study Links Increase in Emergency Heart Events With COVID-19 Vaccine Rollout
A new study found a correlation between an increase in emergency cardiovascular events among people under 40 years of age during the launch of Israel’s COVID-19 vaccine program.
Published in the Nature journal, researchers utilized data from the Israel National Emergency Medical Services between 2019 and 2021 that evaluated emergency, or EMS, calls among 16- to 39-year-olds across Israel “with potential factors including COVID-19 infection and vaccination rates.”
They found that there was a 25 percent increase in EMS calls between January 2021 to May 2021, as compared with the years 2019 and 2020. Israel, which primarily uses Pfizer’s mRNA vaccine, launched its COVID-19 vaccine program in late December 2020.
“The weekly emergency call counts were significantly associated with the rates of 1st and 2nd vaccine doses administered to this age group but were not with COVID-19 infection rates,” they found. “While not establishing causal relationships, the findings raise concerns regarding vaccine-induced undetected severe cardiovascular side-effects and underscore the already established causal relationship between vaccines and myocarditis, a frequent cause of unexpected cardiac arrest in young individuals.”
They recommend that when evaluating possible vaccine side-effects and COVID-19 outcomes, officials should incorporate EMS data and relevant data to identify potential new health trends such as an increase in EMS calls, and “promptly investigate potential underlying causes.”
A recent study carried out by Swedish researchers across populations in Finland, Denmark, Sweden, and Norway suggested that heart inflammation requiring hospital care was more common among people who received COVID-19 vaccines than individuals who did not.
“These extra cases among men aged 16 to 24 correspond to a 5 times increased risk after Comirnaty and 15 times increased risk after Spikevax compared to unvaccinated,” Dr. Rickard Ljung, a professor and physician at the Swedish Medical Products Agency who was involved in the study, told The Epoch Times last week. Spikevax is the name for Moderna’s COVID-19 vaccine, while Comirnaty is Pfizer’s vaccine.
His team found that myocarditis or pericarditis rates are higher than the levels in an unvaccinated cohort, or 38 per 100,000 after second doses of the mRNA vaccines were administered.
The Israeli research team said in their study, published on April 28, that they believe the “benefits of COVID-19 vaccination are clear, especially for populations at great risk of developing serious and potentially life-threatening illness” such as older adults or immunocompromised individuals. However, they noted, “it is important to better understand the potential risks to minimize potential harm.”
When conducting the research, the Israeli scientists made note of several potential flaws, including a “self-reporting bias” when individuals report symptoms via report systems including the U.S. federal government-run Vaccine Adverse Event Reporting System (VAERS), including “under and over-reporting” of vaccine-related symptoms.
“Even the study from Israel that is based on more proactive data collection mentions that some of the potentially relevant cases were not fully investigated,” they said.
A second issue the researchers ran into is how the symptoms of myocarditis, a type of heart inflammation, present themselves.
“Myocarditis is a particularly insidious disease with multiple reported manifestations,” they noted. “There is vast literature that highlights asymptomatic cases of myocarditis, which are often underdiagnosed.”
Meanwhile, “myocardial injury and myocarditis [are] prevalent among patients with COVID-19 infection,” not just among those who received the vaccine, it said.
“As COVID-19 vaccine rollouts often take place with background community COVID-19 infections, it could be challenging to identify whether increased incidence of myocarditis and related cardiovascular conditions … is driven by COVID-19 infections or induced by COVID-19 vaccines,” it added.
The U.S. Centers for Disease Control and Prevention and most health agencies worldwide have said that the benefits of COVID-19 vaccines outweigh the potential risks. The CDC on its website says that most patients who develop myocarditis or pericarditis and got medical care have responded well to treatment.
Symptoms include chest pain, shortness of breath, and feelings of a fast-beating or fluttering heart
https://www.theepochtimes.com/study-links-increase-in-emergency-heart-events-with-covid-19-vaccine-rollout_4435910.html
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Increase in Reactivated Viruses Following COVID-19 Booster Shots: Dr. Richard Urso
Some viruses, after initial infection, remain latent in the body for a lifetime and may reactivate to cause infection again or a different condition. These kinds of latent viruses are being reactivated in a large number of people following their booster COVID-19 shots, causing symptoms of long COVID and other health conditions, according to Dr. Richard Urso.
Long COVID is a condition where people experience ongoing, recurring, or new health problems weeks to months after first being infected with SARS-CoV-2, the virus that causes COVID-19, or receiving a COVID-19 injection. Symptoms may include brain fog, fatigue, chest pain, and insomnia, among others.
“So in my clinic right now, I am seeing three to five people a week because they know that I am taking a lot of time in my practice to do COVID, and they’re coming to see me with long COVID and … with problems after the vaccine,” Urso, an ophthalmologist, a drug design and treatment specialist, and co-founder of the International Alliance of Physicians and Medical Scientists, told EpochTV’s “American Thought Leaders” program. “And what I’m finding is a huge number of them have reactivated Epstein-Barr, herpes simplex, herpes zoster, CMV.”
Of the more than 100 species of herpesviruses, eight are known to infect humans and remain in the body for life after the primary infection has cleared, and which can reactivate later under certain conditions:
Most people are unaware that they’ve been infected with some of these viruses as they experience no symptoms.
“A lot of people are looking at this long COVID as if it’s all viral related problems, specifically to the spike protein or to other issues. They don’t know that we’re seeing this huge reactivation in the herpesvirus family and we have treatment for it. It’s been working really really well,” Urso said.
While there is still no standard clinical definition or treatment for Long COVID, Urso says that there are many different repurposed drugs doctors can prescribe off-label to treat the syndrome, such as those used in the I-RECOVER protocol, developed by The Front Line COVID-19 Critical Care Alliance.
For long COVID symptoms caused by one of the reactivated herpesviruses, Urso says he prescribes Valtrex and supplements like lysine and vitamin D.
“We use lysine because it’s one of those nutritionals that’s good against the herpesvirus family. The ratio of lysine-arginine seems to impact the ability of these viruses to replicate,” Urso said.
He added, “I tell people vitamin D is your data analyst. It allows the immune system to make good decisions … And when vitamin D is around, your immune system can recognize, ‘Oh, this is pollen, let’s leave it alone. Let’s attack this pathogen, let’s attack this cancer.’”
Urso said he’s been recommending vitamin D since 1995 when he was the chief of orbital oncology at MD Anderson Cancer Center. He came upon a study that showed the supplement “had some impact on a tumor recognition protein” and began to test all of his patients’ vitamin D levels.
“Virtually 100 percent of the patients were vitamin D deficient with cancer, colon cancer particularly, we became aware of it,” Urso said, adding that vitamin D has also been “amazing for allergies, it’s amazing for prevention, and resistance against cancer, particularly lymphomas and breast cancer.”
Treating COVID Patients
When the pandemic began, Urso said that he couldn’t stay quiet knowing that COVID-19 can be treated early with various repurposed drugs and “reluctantly started treating” patients as a result of other doctors refusing to prescribe early treatment.
“I told my patients if you have COVID, nobody is going to help you. I said, first go through the chain, [and] if no one’s going to help you, I’ll help you,” Urso said.
More than two years into the pandemic, the Centers for Disease Control and Prevention (CDC) continues to tell people to stay home unless they show “emergency warning signs” that include difficulty breathing, new confusion, and persistent chest pain or pressure.
The health agency only began recommending in January 2022 that individuals at high risk of developing severe disease should seek early treatment with one of the emergency authorized medications when they test positive for COVID-19.
Throughout the pandemic, the CDC has not recommended people to take vitamin D. Studies have shown that vitamin D can help prevent COVID-19, reduce admission to the intensive care unit, and significantly reduce mortality. A study from Israel found that people who were vitamin D deficient were 14 times more likely to have severe COVID-19.
Lipid Nanoparticles
Lipid nanoparticles (LPNs) are tiny particles made up of lipids or fat that act as a delivery system by encapsulating the mRNA that encodes the SARS-CoV-2 spike protein into the human cells.
Without the LPNs, the mRNA would degrade in a matter of seconds once injected into the arm.
Studies have found that the LPNs are not degrading and being eliminated from the body in the 36-hour time frame the FDA recently told The Epoch Times about, nor do they stay only at the injection site.
The Japanese regulatory agency’s biodistribution study (pdf) of the Pfizer vaccine showed that some of the mRNA moved from the injection site and through the bloodstream, and was found in various organs such as the liver, spleen, adrenal glands, and ovaries of rats 48 hours following injection.
“This is something that I would have known quite readily because I work with lipid nanoparticles,” Urso said. “I could have told you that lipid nanoparticles, I usually say, they need a door crack [to leave the injection site], whereas a virus needs an open door.”
Since a normal vaccine requires an “open door” to distribute to other parts of the body, Urso says, “a normal vaccine stays in the arm, pretty much 99.9 percent or 99 percent,” while “a large majority” of LPNs will not stay in the arm.
“In fact, we now know that a large part of it goes into the lymph node right underneath here, and is still making spike protein 60 days later,” Urso said, adding that the spike protein “is actually being found up to 15 months later, in monocytes and other cells, it’s not being degraded.”
Urso says that the persistence of spike protein in different parts of the body is interfering with the immune system’s normal functions and causing health problems.
“It’s blocking important tumor repairing genes called p53, it’s blocking BRCA [genes], it’s also messing with microRNA-27A, which is causing upticks in colon cancer cells,” Urso said.
Urso says that the presence of spikes and LPNs is also “messing with Toll-like receptors 7 and 8,” which are “important for immune surveillance for viruses.”
“So we’re going to see this huge uptick in all the viruses that lay kind of dormant in our body like herpesvirus family.”
https://www.theepochtimes.com/increase-in-reactivated-viruses-following-covid-19-booster-shots-dr-richard-urso_4434667.html
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)
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https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)
https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)
https://westpsychol.blogspot.com/ (The Psychologist -- backup)
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