First COVID Deaths Were Fully Jabbed, Australian State Records Reveal

In light of a court case launched by a group of doctors challenging the Queensland government's COVID-19 vaccination mandates, records have revealed that the first deaths in the Australian state were individuals who were fully vaccinated.

A list of the state’s first 183 COVID-19 deaths from the pandemic's start on March 13, 2020, until Jan. 27, 2022, produced by Queensland’s chief health officer in an affidavit, indicates it was known to authorities as early as Jan. 2022 that the vaccines may not be preventing deaths.

The list shows that the first locally acquired COVID-19 death was one in their 80s and another in their 30s, with both having received two doses of the vaccine in December 2021 and January 2022, respectively.

While Queensland recorded seven deaths early in the pandemic, these cases were acquired outside of the state and before vaccine rollouts began.

Queensland's border opened in December 2021 after 80 percent of the state population vaccination was reached. By Dec. 31, 2021, nearly 90 percent of the population over 16 were fully vaccinated.

The case, which was launched against the state, calls for the September 2021 directive requiring employees in public health and aged-care facilities to be vaccinated against COVID-19 to be revoked.

A specialist from the case, psychiatrist Peter Parry, said that in the three decades of his career, he had never been subject to disciplinary action until now.

“I graduated from medical school 40 years ago and in all that time have never had a single complaint about me presented to a medical board or AHPRA,” he said.

The reason he chose to decline the COVID-19 vaccines was because these are “not normal vaccines.”

“We hope, by bringing evidentiary material and expert witness testimonies before the Supreme Court, that the Justices will look at the evidence and rule in our favour. If successful, large numbers of experienced nurses, allied health, and doctors will be able to return to assist an overstretched Queensland public health system,” he added.

In addition to enforced work mandates, Premier Annastacia Palazczuk barred the unvaccinated from accessing services and freedoms such as hospitals, disability services, aged care, libraries, and hospitality venues.

This was enforced by proof of vaccination requirements at venues, which the Queensland government said was to keep Queenslanders safe.

Messaging Shifts to Reducing Severe Illness

Initially, in 2021, the Queensland Government closed the state's borders and encouraged people to get vaccinated against COVID-19. They aimed to reopen the borders once 80 percent of the population was vaccinated, with the goal of stopping the virus's spread and safeguarding vulnerable citizens.

However, when the borders reopened after reaching the target, COVID-19 cases surged instead of decreasing. When it became clear that the vaccines didn't entirely prevent infection or transmission, the focus of the messaging shifted to highlight the vaccines' effectiveness in reducing severe illness and death.

It is still a condition today for most Queensland health staff to be vaccinated against COVID-19 to ensure the ongoing safety of employees, patients, visitors and the wider community.

“The overwhelming benefits of COVID-19 vaccination continue to outweigh the potential risks, and this is substantiated by enormous amounts of safety data based on billions of doses worldwide,” a spokesperson for the TGA told The Epoch Times in an email.

Pfizer Dismisses Concerns Over Vaccine Mandates

The news of the deaths follows a parliamentary inquiry into the COVID-19 mandates heard from the Australian heads of Pfizer Australia that the vaccine mandates coerced Australians into getting vaccinated for COVID-19, saying they had a choice.

Appearing before an Australian senate inquiry into the COVID-19 vaccine mandates, Pfizer Country Medical Director Dr. Krishan Thiru and Dr. Brian Hewitt, the head of Regulatory Sciences for Pfizer, dismissed concerns of senators that Australians had been coerced into getting the COVID-19 vaccine.

"I believe firmly that nobody was forced to have a vaccine," Dr. Thiru said.

"Mandates for vaccine requirements are determined by governments and health authorities. I believe everybody was offered an opportunity to get a vaccine or not get a vaccine. I don't believe that anybody was forced to take a vaccine."

Meanwhile, Dr. Hewitt, when asked if he believed Australians in states that were subject to large-scale mandates—like Western Australia or Victoria—were not forced into getting the shot even when they found they were unable to earn a living without receiving a vaccination, replied he did not believe mandates compelled individuals into vaccinating.

"The mandates for vaccine requirements are determined by governments and health authorities. I don't believe that the mandates actually forced individuals to get vaccinations," he said.

https://www.theepochtimes.com/world/first-covid-deaths-were-fully-jabbed-australian-state-records-reveal-5480523

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Recent Mask Mandates Lifted Amid Pushback

Kaiser Permanente in Santa Rosa, California, on Aug. 24 reversed a recent policy that would require masks in its hospital after it reinstated the mandate days before. A Hollywood studio also said it would do away with its mandate.

Officials for the hospital system told the Santa Rosa Press Democrat that the mask policy applies only to staff, not patients. It said that it is “strongly encouraging masks for patients, members, and visitors in the hospital and medical offices in the Santa Rosa Service Area in response to this latest increase in COVID-19 cases.”

“Our intent was to communicate that as of Tuesday, we have expanded the masking requirement for our employees and physicians to medical offices and clinic settings; we apologize for any confusion among Press Democrat readers,” Kaiser said in its latest statement.

The statement also said that "visitors, patients, and members are strongly encouraged to also wear masks in these settings,” according to the paper. “We have not changed our masking requirements in the hospital, which have been in effect since April: employees and physicians are required to wear masks and we ask visitors to wear masks when in the hospital.”

It doesn't appear that Kaiser Permanente, which operates hospitals across the United States and California, would also attempt to reinstate mask mandates at other locations.

Days before its latest statement, the hospital system said it would be mandating masks for patients, doctors, patients, visitors, and staff members at its hospital and medical offices.

“Kaiser Permanente Northern California is committed to protecting the safety of our members, patients, employees, physicians, and visitors, which includes taking appropriate steps to prevent the spread of transmissible infectious diseases in our facilities," it told local media.

Some Northern California locals weren't happy with the announcement that mask mandates would return, according to local outlets.

"They told us a bunch of [expletive]," Richard Staudinger, a North Sacramento resident, told CBS. "I think most of the people don't believe it now."

Another, Craig Roberts, said, "I think it's more political than anything, just think they're trying to do what they did in 2020."

But some said they don't mind the mandates. "I don't have a problem if they reinstate the masks," Kiona Cooper, of Northern California, said.

Other Mandates

Meanwhile, the Lionsgate film studio in Santa Monica also said it would not be implementing a mask mandate, days after the media company said it would force workers to put on masks again on certain floors. It claimed that it never changed its mask policy.

“The LA County Department of Public Health notified us yesterday that we could lift the mask requirements, effective immediately, and we have," the firm told news outlets over the weekend.

The statement also said: "Lionsgate never changed its own mask policy. The LA County Department of Health ordered us to institute the temporary masking requirement after we reported a cluster of COVID cases to them and we have an obligation to comply with their orders."

Last week, a Lionsgate memo stated that employees on only certain floors have to wear surgical masks, KN95 masks, or N95 masks "except when alone in an office with the door closed, actively eating, actively drinking at their desk or workstation, or if they are the only individual present in a large open workspace.”

Earlier in the month, data from the Centers for Disease Control and Prevention showed that COVID-19 hospitalizations rose across the country. Hospitalizations rose by 21.6 percent, to 12,612 new admissions from 10,370, according to the data ending Aug. 12.

Despite the increase, it’s among the lowest levels of hospitalization recorded since the start of the pandemic in early 2020.

“An upswing is not a surge; it’s not even a wave,” Dr. Shira Doron, the chief infection control officer for Tufts Medicine, told ABC News. “What we’re seeing is a very gradual and small upward trajectory of cases and hospitalizations, without deaths really going along, which is great news.”

At the same time, several hospitals, including some in upstate New York, and Morris Brown College in Atlanta reimplemented mask mandates, prompting concerns about a broader effort to force masks on people, three years after the start of the pandemic in the United States. Media coverage around the small increase in COVID-19 cases has also focused on whether masks should be worn, with mainstream outlets such as CNN interviewing doctors who say people should start wearing them again.

But some politicians and commentators, in response, called on supporters to resist the mandates.

“It’s alarming that the mandates are kicking in again,” Sen. Ron Johnson (R-Wis.) said in a recent interview. “It’s like, OK, we noticed masks didn’t work, particularly for children. We always knew they didn’t work for kids.”

It also comes as President Joe Biden on Aug. 25 told reporters in Lake Tahoe that he signed off on a proposal "to present to Congress a request for additional funding for a new vaccine that is necessary, that works."

https://www.theepochtimes.com/us/recent-mask-mandates-lifted-amid-pushback-5481484

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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)

http://jonjayray.com/blogall.html More blogs

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Will Heavily COVID-19 Vaccinated Populations Experience High Incidence of Cancer & Autoimmune Disease?

A frequent contributor to TrialSite, Geert Vanden Bossche, the Belgium-based vaccinologist has spent the last few years of the pandemic intensely studying not only SARS-CoV-2 and mass vaccination but also the immunological considerations, and risks, associated with the vaccination drives.

In this latest paper “Immunological correlates of vaccine breakthrough infections caused by SARS-CoV-2 variants in highly C-19 vaccinated populations,” Vanden Bossche unleashes a truly dark, complex, and what he believes is thorough hypotheses suggesting heavily COVID-19 vaccinated populations will experience crisis levels of cancer and autoimmune disease.

Why will this tragedy occur? According to Vanden Bossche, “In highly Covid-19 (C-19) vaccinated populations, an increase in IgG4 antibody (Ab) titers following steric immune refocusing (SIR)- enabling PNNAb1-dependent vaccine breakthrough infections (VBTIs) with infectious SARS-CoV-2 (SC-2) immune escape variants promoted generalized hyposensitization to ‘foreign’ and hypersensitization to ‘self’.” Arguing that the process of hyposensitization (train immune system to become less reactive to allergen over time) “to ‘foreign’ leads to an “anti-inflammatory effect” and thus reducing the prospect for autoimmune-like disease symptoms, so-called ‘hypersensitization’ (heightened immune reaction) to ‘self’ will lead to surges in incidence of cancer and autoimmune disease.

Vanden Bossche’ s hypothesis suggests that in a highly COVID-19 vaccinated populations, there is a greater incidence of cancer and autoimmune disease. Looking into surges of IgG4 antibody titers first should be understood.

A subclass of immunoglobulin G (IgG) antibodies which are a type of antibody generated by the immune system to help protect the body against infections and other foreign substances, they play a crucial role in the immune response by recognizing and binding to specific antigens, such as bacteria, viruses and other pathogens.

TrialSite recently summarized research out of Hungary suggesting that COVID-19 vaccines trigger higher levels of spike specific IgG than persons infected with SARS-CoV-2, the virus behind COVID-19.

This was according to a team of physicians and scientists employed in Internal Medicine and the Immunology and Hematology Research Group in Semmelweis University- Eötvös Loránd Research Network (Office for Supported Research Groups), Budapest Hungary. They investigated the SARS-CoV-2 infection and the vaccination induced a similar spike-specific IgG subclass pattern. With this study involving 47 healthy volunteers for the vaccinated cohort in Budapest Hungary, an important aim was to determine if these patterns have been influenced by the chronological order of natural virus infection and vaccination or not. Also monitoring the concentration of each spike-specific IgG subclass over a three-to-four-month period the Budapest-based investigators sought to estimate the stability of the antiviral humoral immune response.

Importantly, IgG 4 antibodies are generally less understood than other subclasses of IgG. Involved in immune tolerance, and with anti-inflammatory properties, IgG4 responses are associated with chronic infections, allergies and autoimmune diseases. Interestingly, unlike other subclasses, IgG4 antibodies can undergo a process called “Fab-arm exchange” where the arms of two different IgG4 antibodies can be swapped, potentially altering their function.

Back to Vanden Bossche, with an increase in IgG4 titers due to what he describes as “steric immune refocusing” (SIR), defined in another paper of his as “re-orientation of the humoral S-directed immune response towards more conserved, immune subdominant S-associated epitopes as a result of steric masking of variable, immunodominant S protein-associated epitopes by pre-existing, low-affinity pNAbs” the latter signifying human performed natural antibodies.

So, PNNAb1-dependent vaccine breakthrough infections or “VBTIs” lead to “infectious SARS-CoV-2 (SC-2) immune escape variants promoted generalized hyposensitization to ‘foreign’ and hypersensitization to ‘self’, inducing carcinogenicity and autoreactivity.”

Not a good development if this comes true. Vanden Bossche is known for predicting select adverse outcomes as a result of the ongoing mass COVID-19 vaccination approach to the pandemic. For example, the Belgium-based vaccinologist predicted that introducing mass vaccination in the midst of the SARS-Cov-2 pandemic would place great evolutionary pressures on the pathogen, supporting the evolutionary process. Most certainly SARS-Cov-2 mutated into many different variants and strains. However, we can’t be sure if it's due to Vanden Bossche’ s hypothesis but it should be vetted by experts in the field.

But ominously, here in heavily vaccinated populations Vanden Bossche’s hypothesis suggests a tragic explosion in cancer and autoimmune disease.

That's because according to his hypothesis, “SIR-enabling VBTIs, but also mRNA vaccination, facilitates immune refocusing to more conserved, immune subdominant spike (S)-associated epitopes.” Remember, epitopes are specific regions on the surface of antigens to which antibodies or immune cells bind. They play a crucial role in the immune system’s ability to recognize and respond to foreign substances such as viruses.

So, what’ s a key part of this mechanism that leads to serious trouble—namely higher incidence of cancer and autoimmune disease?

According to Vanden Bossche’ s paper, “delayed maturation of these de novo (new) primed, subneutralizing Abs into isotype-switched IgG4 anti-S Abs enables prolonged immune pressure on viral infectiousness.” What does this do? It leads to real trouble in the form of “promoting large-scale co-circulation of more infectious SC_2 immune escape variants.”

It is a cascade of immune selection events that “eventually mitigate disease caused by SC-2 and other unrelated viral pathogens (via anti-inflammatory IgG4)” leads to viral dissemination.

Vanden Bossche hypothesizes that “acute autoimmune disease and early-onset cancer in highly C-19 vaccinated populations are due to VBTI-or mRNA vaccine-mediated immune refocusing to more conserved, poorly immunogenic ‘self-like’ epitopes.

https://www.trialsitenews.com/a/will-heavily-covid-19-vaccinated-populations-experience-high-incidence-of-cancer-autoimmune-disease-4e88ff91

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Sen. Johnson Sounds Alarm on Return of COVID-19 Mask Mandates

Sen. Ron Johnson (R-Wis.) is sounding the alarm after a small number of offices, hospitals, and schools reinstated mask mandates in recent days.

Describing the mandates as “alarming,” Mr. Johnson told the Moms for Liberty group on Aug. 23 that they are ineffective and said he would keep fighting them.

“It’s alarming that the mandates are kicking in again,” he told the group. “It’s like, OK, we noticed masks didn’t work, particularly for children. We always knew they didn’t work for kids.”

The Wisconsin Republican said, “N-95 masks can have some marginal benefits—but not to deny people freedom.”

Mr. Johnson has said he was always skeptical of federal vaccine mandates and has been an advocate for people who claimed to have been injured by COVID-19 vaccines. He also called on the Biden administration to admit that its COVID-19 policies didn’t work.

“They’ll never admit they were wrong in how they handled COVID. I don’t see how anybody can take a look at how the federal government—really, over the course of two administrations—how they handled COVID, and say it was anything but a complete and miserable failure,” he told the Washington Examiner in May.

The White House, the senator added, won’t acknowledge what he described as the “the incalculable human toll” and the “economic devastation caused by the shutdowns.”

Mr. Johnson’s recent remarks come after Hollywood studio Lionsgate said in a memo earlier this week that it would reimpose a mask mandate for several floors of its office in Santa Monica, California.

“Employees must wear a medical grade face covering (surgical mask, KN95 or N95) when indoors except when alone in an office with the door closed, actively eating, actively drinking at their desk or workstation, or if they are the only individual present in a large open workspace,” a Lionsgate manager said in a memo, reported by Deadline.

This week, Kaiser Permanente Hospital in Santa Rosa, California, and the Upstate Community Hospital in Syracuse, New York, brought back the masking rule for visitors, patients, nurses, and doctors.

“To ensure that we are helping protect the health and safety of our patients, our workforce, and our community, we have reintroduced a mask mandate for physicians, staff, patients, members, and visitors in the hospital and medical offices in the Santa Rosa Service Area,” Kaiser Permanente said.

Morris Brown College in Atlanta also said that masks will again be required on campus because of a rise in cases on a larger campus in Atlanta.

“There will be no parties or large student events on campus for the next two weeks,” the school said.

At the same time, there has been an increase in media coverage of several COVID-19 variants, including one that the U.S. Centers for Disease Control and Prevention (CDC) stated could potentially evade vaccines. No federal agencies have announced any new mask mandates or recommendations.

Media Coverage

In recent days, an increasing number of television doctors have made suggestions that some people start masking again.

“It’s riskier that you will get infected now than it was a month or two ago, without question, probably twice as risky,” Dr. Bob Wachter, chair of medicine at the University of San Francisco, told CNN in a recent interview. “If you’re trying to be careful, it’s time to whip out the mask again.”

Also appearing on CNN, Dr. Jonathan Reiner, a cardiologist in Washington, said on Aug. 22 that people who are at risk from a COVID-19 infection—including people aged 65 and older—should put masks on again. He also said that President Joe Biden should do so, too.

“Octogenarians comprise the highest-risk group for complications following COVID infection,” he said. “At least until the numbers start to drop again, it would be appropriate for President Biden to take some precautions and wear a mask in crowds.”

Last week, COVID-19 hospitalizations rose across the country, according to data from the CDC. Hospitalizations rose by 21.6 percent, to 12,612 new admissions from 10,370, according to the data ending Aug. 12.

Despite the increase, it’s among the lowest levels of hospitalization recorded since the start of the pandemic in early 2020.

“An upswing is not a surge; it’s not even a wave,” Dr. Shira Doron, the chief infection control officer for Tufts Medicine, told ABC News this week. “What we’re seeing is a very gradual and small upward trajectory of cases and hospitalizations, without deaths really going along, which is great news.”

https://www.theepochtimes.com/health/senator-sounds-the-alarm-on-return-of-covid-19-mask-mandates-5480124

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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)

http://jonjayray.com/blogall.html More blogs

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Biden’s probe censored Covid ‘smoking gun’

Mr Biden ordered the Intelligence Community in May 2021 to give him an assessment into how the pandemic began after revelations, first published by The Australian, that researchers at the Wuhan Institute of Virology had been hospitalised with Covid-like symptoms in November 2019 in the suspected first cluster of the pandemic.

When the report was published it concluded that most intelligence agencies assessed the virus, even if it had leaked from the Wuhan Institute of Virology, was natural rather than manipulated in a laboratory

The Australian can reveal that this was not the assessments made by the four groups within the intelligence agencies that actually engaged in scientific analysis, who concurred that there was either a highly likely or reasonable chance the virus was genetically engineered.

At least 90 per cent of the work from one of those agencies — the Pentagon’s top intelligence group — was censored in the final report and Defence Department scientists were told to stop working with the FBI on their findings.

Scientists at the Defense Intelligence Agency’s National Centre for Medical Intelligence (DIA NCMI) had conducted rigorous research on the genomic sequence of the virus and firmly concluded that it was, most likely, a laboratory construct.

Well-placed sources familiar with the work that unfolded inside the intelligence agency and their interactions with the Office of the Director of National Intelligence for the 90-day probe spoke to The Australian for this investigation.

Covid-19 origin ‘smoking gun’

Their internal research at the Pentagon-based agency led to a finding that was described internally as a “smoking gun.”

One of the scientists discovered that the size and location of a fragment of Covid-19 resembled the same fragment in Wuhan Institute of Virology research from more than a decade earlier, in 2008. It was the same technique that the WIV had used in grant applications to make chimeric viruses.

“This paper is the smoking gun of everything. When the team reviewed this data, they thought ‘This is created in the lab. It’s a reverse genetics construct,” a source said.

But their input into the 90-day origins probe was censored.

Sources close to the inquiry estimated that about 90 per cent of the DIA NCMI edits were deleted or censored or simply weren’t included.

“They said the information was too technical to include in the ODNI assessment,” a source familiar with the process told The Australian.

“When the scientists saw the final document, they wondered were did all their edits go?”

They had been working with the FBI’s Weapons of Mass Destruction unit, until the co-operation between the two agencies was blocked, with a director at the Defense Intelligence Agency claiming the FBI was “off the reservation” on the topic of the origins of Covid-19.

The 90-day study also ignored coronavirus gain-of-function research underway in Wuhan and there was a lack of genomic data analysis.

The scientific team inside the DIA thought the 90-day report was scientifically inaccurate, according to sources familiar with the inquiry.

“There was a lot of erroneous information. There was no genomic analysis in the ODNI report, nothing about the rare codons or the poly basic cleavage site and the minimal cassette that is similar to prior work published by WIV scientists. This virus also had no apparent mutational signatures,” a source involved in the inquiry said.

https://www.theaustralian.com.au/nation/covid19-origin-joe-bidens-wuhan-probe-censored-pentagon-scientists-who-concluded-it-was-genetically-engineered/news-story/25dc85912c348e009ced79f69acc8e2e

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US Congress to probe claims Covid report was censored by intelligence community

The US congress is set to probe revelations that officials at the highest levels of the intelligence community censored the input of scientists who concluded that Covid-19 was genetically engineered in a laboratory.

A homeland security committee senator has also called for the allegations to be “investigated immediately”.

The Australian and Sky News revealed on Friday that senior scientists working for the Defence Intelligence Organisation’s National Centre for Medical Intelligence – Robert Greg Cutlip, Jean-Paul Chretien and John Hardham – had 90 per cent of their input into a probe ordered by US President Joe Biden deleted.

They were stunned when the Office of the Director of National Intelligence’s study into the origins of Covid-19 was released and downplayed the likelihood that SARS-CoV-2 was the result of laboratory research at the Wuhan Institute of Virology.

US officials have expressed serious concerns at censorship of the scientists, saying the matter raised questions over the accuracy of the 90-day probe handed down by Mr Biden in August 2021.

The congressional select subcommittee on the coronavirus pandemic will now evaluate the allegations, with a spokesperson saying there were concerns about the accuracy of the intelligence agency’s public assessments.

“The select subcommittee on the coronavirus pandemic takes the reported allegations seriously,” a spokesperson said. “We are explicitly tasked with investigating the origins of Covid-19 and the purported information raises questions concerning the accuracy of the ODNI report and its conclusions.”

Separately, US senator Roger Marshall, who sits on the Homeland Security and Governmental Affairs Committee and is leading the Covid origins investigations, said he was exploring his options about how to take censorship of the scientists further and that the cover-up “must be fully investigated immediately”.

“We never trusted the Chinese Communist Party to come clean about the origins of Covid-19, but a potential cover-up by our own government and Defence agencies tasked with securing our ­nation should concern every American and must be fully investigated immediately,” he told The Weekend Australian.

“The intelligence community’s official inconclusive position about the origins of Covid-19 has never accurately reflected the classified intelligence we reviewed. Now we are learning insider censorship of US expert scientists may have influenced the report.”

Quantitative biologist Justin Kinney, associate professor at Cold Spring Harbor Laboratory, said the revelations were “very important”.

“The ODNI appeared to have intentionally suppressed critical scientific information to mislead the public about the origins of Covid-19,” he said. “The house subcommittee on the pandemic should investigate.”

It comes after The Australian and Sky News revealed a draft document was shared with agencies in the intelligence community for input when Mr Biden ordered the probe in May 2021.

Sources familiar with the work inside the ­intelligence agency and the scientists’ interactions with the ODNI said 90 per cent of their input was censored or deleted.

“They said the information was too technical to include in the ODNI assessment,” one said.

“When the scientists saw the final document, they wondered where did all their edits go?”

https://www.theaustralian.com.au/nation/us-congress-to-probe-claims-covid-report-was-censored-by-intelligence-community/news-story/798d862288dadc33082561bd8739e662

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Author of Congressional Vax Injury Compensation Bill Pens an Op-Ed

While the Biden administration recently announced another $1 billion for long Covid treatment research and up to $5 billion to develop more vaccines and therapies targeting Covid, a subject lurking just beneath the surface, individuals injured by the Covid vaccine for the most part go unacknowledged and even censored.

One advocate for the vaccine injured claims people have been suffering for too long without any government acknowledgement and it is time for action. “To live in a world where people harmed by a medication are treated with mercy instead of censorship, people must make their voices heard.” Action has been taken, including on the part of TrialSite, which covers the topic objectively as well as engages in partnership with organizations like React19, a Covid vaccine injury group, and offers vaccine injury support groups. Now, it looks as if the United States government is finally responding.

Bill to modernize vaccine compensation+

Democrat Representative Lloyd Doggett from Texas and Republican Congressman Lloyd Smucker of Pennsylvania introduced a bill, H.R.5142, which is designed to modernize the current COVID-19 vaccine compensation schemes. The bill would update and improve the nearly forty-year-old Vaccine Injury Compensation Program (VICP).

Doggett had been reluctant to criticize the Covid vaccine, but recently came out and said, “Vaccines save lives, but in the rarest of cases, usually caused by an error in administration rather than the vaccine itself, they involve injury. While strongly disagreeing with the dangerous misinformation spread by anti-vaxxers, I believe that those who suffer rare injuries associated with vaccines, including those to fight COVID-19, should receive prompt, reasonable compensation for medical bills and other losses. The existing program involves unreasonable delays and inadequate redress. Our bill would update the program and correct the unjust decision to have COVID-19 claims considered by a separate, and even more inadequate governmental program. By assuring a prompt and fair response to any related injury, we build confidence in vaccines and reduce hesitancy.”

Doggett op-ed

In an article in The Hill, Congressman Doggett wrote that Congress must act to modernize the approach to “rare vaccine injuries”. The politician points out the Covid vaccine was needed as a response to the pandemic and was successful. But, he adds, vaccine hesitancy was an issue which had to be dealt with. Doggett adds one way to assure people the vaccines are safe is to make sure there is trust in the vaccines and the government is to make sure there is a program to safely and fairly compensate people who have suffered a vaccine injury.

The Congressman points out because of the uniqueness of the situation with the Covid vaccine, compensation for Covid vaccine injury was considered under the Countermeasures Injury Compensation Program (CICP). The CICP has been an “abject failure” in dealing with Covid vaccine injuries, and now, finally, politicians are aware of the situation. And, as Doggett points out, with all the claims made to the CICP, a pittance has been paid out by the agency scheme.

Doggett and Smucker’s bill is called The Vaccine Injury Compensation Modernization Act, which aims to update the CICP and provide “much needed” relief to people whose vaccine injury claims have been lingering. “Our legislation authorizes the resources and additional judges required to review claims expeditiously, as well as reforms to provide more reasonable time for filing a claim. It streamlines the addition of future vaccines to the program, a process now too frequently delayed by bureaucratic red tape.”

The payouts will also account for work loss compensation, medical costs and damages. The legislation would also raise the cap in line with inflation, indexing it moving forward.

Frankly why wouldn’t we compensate individuals that have legitimate, verified injuries associated with the vaccine? Again, the Biden administration continues to commit billions into new vaccine and medicinal development, yet no mention of vaccine injury compensation.

But some elected officials in Washington are starting to realize that a fair, reasonably expedited and funded compensation program makes sense.

https://www.trialsitenews.com/a/author-of-congressional-vax-injury-compensation-bill-pens-an-op-ed-c04bd151

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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)

http://jonjayray.com/blogall.html More blogs

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The Highly Mutated BA.2.86, the Detecting Lab and Immunity Questions
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Yesterday, TrialSite reported that the Centers for Disease Control and Prevention (CDC) picked up on a new SARS-CoV-2 variant, one highly mutated, termed BA.2.86. In the United States, the mutated variant was sequenced in Michigan thanks to the ongoing surveillance occurring at the University of Michigan Clinical Microbiology Laboratory.

The University of Michigan Clinical Microbiology Laboratory in the report is termed the originating lab, while the submitting lab was the Lauring Lab, University of Michigan, Department of Microbiology and Immunology. This lab is led by Adam Lauring, M.D., Ph.D., a Professor of Internal Medicine, Infectious Disease and Microbiology & Immunology.

The Clinical Microbiology Lab is led by Michael Bachman, M.D., Ph.D., and Paul R. Lephart, Ph.D., D(ABMM), both Associate Directors of the prominent Midwestern lab—one staffed by 55 medical technologists and clinical laboratory scientists. The laboratories provide service 365 days a year to meet the medical needs of Michigan Medicine and the clients of the “M-Labs” program.

The Clinical Microbiology Laboratory has close ties with Adult and Pediatric Infectious Diseases, the Infection Control Program, the Department of Pharmacy, and the School of Public Health. Close collaboration is key among the various functional areas, thus providing the ongoing analysis of interactions between organisms and antimicrobial agents that allow for dynamic reporting to clinicians on the floors and foster productive research collaborations that directly result in improving the quality of care provided to patients.

The Clinical Microbiology Laboratories are accredited by the College of American Pathologists (CAP) and active in the CAP Laboratory Accreditation and Proficiency Testing programs

More on the variant

CBS News coverage of the latest variant discovered revealed some useful information. Kathleen Conley, a CDC spokesperson told the network news, “Today we are more prepared than ever to detect and respond to changes in the COVID-19 virus.” Conley empathized that “Scientists are working now to understand more about the newly identified lineage in these four cases and we will share more information as it becomes available.”

Alexander Tin covered the story for CBS News HealthWatch.

Is BA.2.86 a more threatening or dangerous variant of SARS-CoV-2? Will it lead to more severe COVID-19? While the World Health Organization went on the record that the variant includes dozens of genetic changes, for comparison it’s a similar situation in some ways to how Omicron emerged as a materially different stain than, say, delta.

But public health agencies and academic research centers need more data to determine the risk levels associated with BA.2.86. TrialSite reported that this newly detected strain has been detected in Israel and Denmark as well.

The concern, among other things, is that the mutations could aid the pathogen in its ability to evade immunity, both of the natural (previous infection) as well as vaccine-induced type. There is no real threat at this point given the pathogen has only been detected in a few places. Also, it may well be the case that the human body’s current immune responses help fight off the mutant. Or for that matter, the mutant may not be able to compete with existing highly infectious strains.

CBS News obtained a presentation from a Fred Hutch Cancer Center evolutionary biologist, Jesse Bloom, Ph.D., conveying what could be considered potentially disturbing information about the latest variant. “Deep mutational scanning indicates BA.2.86 variant will have equal or greater escape than XBB.1.5 from antibodies elicited by pre-omicron and first-generation Omicron variants.”

Some of the mutations exist in parts of the virus that could help it evade immunity provided by prior vaccination or infection.

But Bloom also suggested the collective immunity may well be ready to take on BA.2.86, “[T]here are also broader mechanisms of immunity elicited by vaccination and infection that provide some protection against severe disease even for very heavily mutated variants.”

What are the implications for the latest vaccine that will likely be approved by FDA, and recommended by CDC for the fall season?

A monovalent mRNA vaccine produced by both Pfizer-BioNTech and Moderna are under clinical study. TrialSite reported on a trial site looking to enroll adolescents in Cincinnati Ohio for the Moderna clinical trial.

The FDA recommended that the vaccine makers tailor this COVID-19 season’s vaccine to XBB.1.5, an Omicron variant. As TrialSite has reported recently, while this strain predominated circulating Omicron variants across America just a few months ago it is now at 10.3% or lower. TrialSite estimates that by October XBB.1.5 will be under 5% of all circulating SARS-CoV-2 variants, if not less.

What does this mean for COVID-19 vaccine effectiveness? And what about the emerging predominant variants? For example, EG.5 at over 17% of SARS-CoV-2 cases according to the CDC now is the pathogen to watch. The good news for vaccination and natural immunity supporters---EG.5 is an XBB descendent so perhaps the vaccine’s effectiveness will be better than expected. Or perhaps Moderna pointed out, according to CBS News, that its shot provides "a significant boost in neutralizing antibodies" for EG.5.

Yet according to the Fred Hutch evolutionary biologist Jesse Bloom, all bets are off if BA.2.86 is able to outcompete and overcome other fast-moving, mutating Omicron variants. That scenario could represent trouble for our collective immunity. BA.2.86 heavily mutated would be a “fairly poor match” for the current vaccines under clinical development which again target XBB.

A reminder tempering the concern. With each progressive mutation under the Omicron umbrella of variants, COVID-19 becomes ever milder all things considered. And there are treatments available. Yes, it still can turn severe and even deadly but the case fatality rate now ranks with influenza, if not even less dangerous for healthy people.

Even during the Delta variant surge TrialSite always reminded that 90-95% of the COVID-19 cases were mild to moderate, but that persons in high-risk categories (e.g., elderly, persons with comorbidities, immunocompromised) faced considerably higher threat. TrialSite emphasized with national and state public health agencies that face a U.S. population with a staggering reality—about 70% of the adult population is either overweight or obese as reported by Harvard T.H. Chan School of Public Health. During the pandemic, there was little time to risk stratify, and obesity itself was/and is a risk factor. Meaning a good half, of the country’s adults likely fell in the higher risk category. This remains so, although the case fatality rate is under 1%. But generally, the Omicron variants are more infectious, meaning they spread faster, yet overall lead to milder outcomes.

https://www.trialsitenews.com/a/the-highly-mutated-ba.2.86-the-detecting-lab-and-immunity-questions-ffd83b51

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Murdoch Children’s Bombshell: Medicinal Value of COVID-19 Vaccines Now Questionable Among Healthy Children

According to researchers at Australia’s Murdoch Children’s Research Institute, COVID-19 vaccines have demonstrated efficacy against severe incidence of SARS-CoV-2 in children and adolescents, but their value proposition as a mass medical tool becomes questionable considering the unfolding dynamics of today: high pre-existing infection and low risk when infected.

Researchers led by John Hart from the academic medical center for young people Down Under acknowledge that most children now have been infected by SARS-CoV-2, meaning they have built up immunity, and the vaccine’s benefit in healthy children is minimal. They argue any energies and attention placed on COVID-19 vaccination campaigns should be used to advocate for vaccines known to offer higher medical value, such as the measles vaccine. The ramifications of this recent set of findings are substantial.

Published in the BMJ Pediatrics Open, the international review was led by medical researchers from the Australian medical institute. They explored the challenges and considerations of COVID-19 vaccination, especially in low-and middle-income countries with high levels of community transmission and infection-derived immunity.

The team’s review, led by Hart, a medical epidemiologist, suggests that any COVID-19 vaccination scheme moving forward, especially in low-and middle-income countries should be coupled with routine childhood vaccination program that the researchers acknowledge “have greater impact on illness and death, including for measles, pneumonia and diarrheal disease.”

Mild for most

The Australian team found that about two-thirds of all young people that had COVIS-19 and were hospitalized in the first two years of the COVID-19 pandemic did not require medical intervention. Deaths, the investigators reported, “were extremely rare in children.”

Closing in on child herd immunity?

The researchers also point out that the vast majority of children have been infected with SARS-CoV-2. As immunity has increased over time, the disease continues to evolve. Prior research led by Murdoch Children’s found that croup, triggered by the novel coronavirus, declined in 2022 despite the rise of new variants.

Also, data from the Pediatric Active Enhanced Disease Surveillance (PAEDS) network in America found that rates of pediatric multisystem inflammatory syndrome (PIMS-TS), what was a major driver for childhood vaccination, were “Substantially lower during the Omicron COVID-19 variant period.” TrialSite reported on similar findings in the UK.

Net takeaway

While there are still cases where COVID-19 vaccination is recommended, the Australian researchers are clear—they value of these vaccines for children has markedly diminished. In fact, they use the COVID-19 vaccination push as a primary means of promoting more substantive medical vaccination, such as measles. Reading between the lines, and on the face of the piece, the investigators are more concerned about standard vaccination rates, especially in low-and moderate-income countries.

One takeaway called out by this independent media, children achieved herd immunity against SARS-CoV-2 by infection, not vaccination.

https://www.trialsitenews.com/a/murdoch-childrens-bombshell-medicinal-value-of-covid-19-vaccines-now-questionable-among-healthy-children-86a9dada

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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)

http://jonjayray.com/blogall.html More blogs

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What You Need to Know About New ‘Eris’ COVID Variant

The new COVID-19 virus variant spreading now, “Eris,” is currently the predominant strain in the United States, according to data from the U.S. Centers for Disease Control and Prevention (CDC). Although it’s increasingly reported worldwide, health experts say it poses a low risk to public health, as there is no evidence it causes different or more severe symptoms than previous omicron offspring.

The Essentials

A subvariant of the omicron lineage, Eris, otherwise known as EG.5, was detected as early as February 2023. As of Aug. 23, Eris has been detected in more than 50 countries and is responsible for an estimated 20.6 percent of all cases in the United States.

Meanwhile, FL.1.5.1 is now the second most prevalent strain, accounting for over 13 percent of cases.

On Aug. 9, the World Health Organization (WHO) designated Eris as a variant of interest (pdf), meaning it possesses genetic characteristics that could increase its transmissibility, virulence, and ability to evade vaccines.

The WHO had previously labeled Eris as a variant “under monitoring” after a surge in COVID-19 infections in early July.

The current variant of interest list also includes two other omicron cousins—XBB.1.5 and XBB.1.16.

If Eris is upgraded to a variant of concern, governments would need to increase preventative measures, such as mask mandates in hospitals, testing, or physical distancing.

There have already been growing concerns that Eris could trigger governments to revive some COVID-19 restrictions.

How Dangerous Is It Compared to Other Variants?

Eris is a descendent of omicron variant XBB.1.9.2.

Eris carries an additional amino acid mutation, known as F456L, in the spike protein. This mutation has been shown to escape immunity gained from previous variants and may help the new variant transmit quickly.

The CDC said there is no evidence Eris causes more severe disease than other omicron descendants, and it seems to cause similar symptoms.

Similar to those of earlier COVID-19 virus strains and that of the common cold, symptoms may include the following:

Fatigue.
Muscle pain.
Chest pain.
Headache.
Sore throat.
Runny nose.
Congestion.
Cough.
Fever and chills.
Nausea or vomiting.
Diarrhea.
Loss of taste or smell.

New Generation ‘Variant Under Monitoring’

Health authorities have also been tracking a highly mutated strain called BA.2.86, or “Pirola” by some, which has caught scientists by surprise after it was picked up by COVID-19 testing on three continents.

This variant has scientists on alert because its emergence is reminiscent of the early days of the omicron variant in late 2021 when researchers in southern Africa noticed a lineage that quickly spread globally.

“There’s a little bit of déjà vu all over again,” said Adam Lauring, a virologist and infectious-disease physician at the University of Michigan in Ann Arbor, whose lab identified one individual infected with BA.2.86, in an interview with Nature.

Health authorities first detected BA.2.86 in Denmark on July 24, and it has also been spotted in the UK, United States, and Israel.

None of the cases appears to be linked, including three infections in Denmark found in different parts of the country. This geographical distribution is another feature of BA.2.86 that is garnering scientists’ attention.

This suggests the variant may already be fairly widespread, Jesse Bloom, a viral evolutionary biologist at the Fred Hutchinson Cancer Center in Seattle, told Nature. “It’s got to have been transmitting a fair amount.”

The UK Health Security Agency said a recent case was reported in a person with no recent travel history, “suggesting a degree of community transmission within the UK.”

However, experts do not expect BA.2.86 to have the same impact as omicron due to response practice with earlier COVID-19 waves and vaccine rollouts. “There’s good reason to think it won’t be like the omicron wave, but it’s early days,” Mr. Lauring said in the Nature interview.

Current Vaccines

Pfizer, Moderna, and Novavax have created new versions of their vaccines to target another omicron sublineage—XBB.1.5—similar to Eris, so health authorities hope the vaccines will work on new variants.

However, according to the WHO, the F456L mutation Eris carries has been shown to decrease the neutralization of most XBB.1.5 neutralizing antibodies.

Listed by the WHO as a “variant of concern,” XBB.1.5 previously dominated transmission in the United States for several months straight but was surpassed by XBB.1.16, or Arcturus, in July.

The new CDC director, Dr. Mandy Cohen, anticipates that these vaccines will be available at common locations such as pharmacies and anticipates an annual COVID-19 shot, integrating it into routine health practices.

https://www.theepochtimes.com/health/what-you-need-to-know-about-new-eris-covid-variant-5477514

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Another Covid Medication Gets authorization from FDA Despite a Phase 3 “Miss”

When the Covid pandemic started, there was a rush to find a vaccine to combat the disease. Initially, issues arose with the Johnson and Johnson shot and it was discontinued, but the Pfizer mRNA jab was approved. Both shots were authorized by the Food and Drug Administration (FDA) under emergency use authorization (EUA) although the Johnson and Johnson’s (Janssen) authorization was later revoked. The mRNA jabs were later formally approved. But questions still arose over whether or not the Pfizer and later Moderna vaccines were fully vetted before EUA was granted. Now it appears history has repeated itself.

Known as vilobelimab, this experimental product now available on an emergency basis was developed via human-mouse chimeric IgG4 kappa antibody targeting human C5a in plasma.

Gohibic gets EUA

In April, the FDA granted emergency use authorization for the use of the Gohibic injection for the treatment of Covid-19 in hospitalized adults. The medication is to be used within 48 hours of a patient who’s been intubated or is on a heart-lung machine. The press release for the medication says, “There is limited information known about the safety or effectiveness of using GOHIBIC to treat people in the hospital with COVID-19.

Available results from clinical trials in adults indicate that treatment with GOHIBIC may decrease the risk of dying in hospitalized adults with COVID-19 when initiated within 48 hours of receiving IMV or ECMO. The safety and effectiveness of GOHIBIC have not been studied in children hospitalized with COVID-19.”

Authorized despite Phase 3 “miss”

According to the FDA, the Gohibic clinical trial showed that patients treated with the drug had a lower risk of death by day 28 and day 60 of treatment compared to placebo. However, there is a phase 3 clinical trial “twist”. In a randomized trial, Gohibic reduced the risk of death in the sickest patients by 27% compared with placebo during a 28-day period. In that trial, the drug missed “statistical significance” on the trial’s primary endpoint. But in another analysis and two other post hoc analyses the medication’s improvement was significant. The treatment targets inflammation that leads to progression of the Covid virus.

Drug maker talks to FDA

Despite the results of the trial, the maker of Gohibic, InflaRx, talked to the FDA and then applied for the EUA last September. InflaRx was founded in 2007 in Germany and has offices in Ann Arbor, Michigan. In a press release, the Chief Executive Officer (CEO) of InflaRx, Niels Riedemann said that Gohibic will bring hope to Covid patients who despite vaccines and other treatment options, are still developing viral sepsis and are progressing to critical status.

The company has a supply of Gohibic which is readily available, but Riedemann didn’t reveal the price of the medication. However, he did expect to charge a five-digit figure per patient for the drug. Once again, it appears Covid is a continual cash cow for Big Pharma CEOs.

https://www.trialsitenews.com/a/another-covid-medication-gets-eua-from-fda-despite-a-phase-3-miss-de19c4dc

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The World’s Longest Natural Experiment on Vaccine Efficacy

Lack of controls in evaluating vaccine efficacy makes all inferences speculative

In early 2021, the COVID-19 vaccine campaign was launched, based on clinical findings of 95% efficacy in late 2020 (Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine).

But this efficacy relied on relative risk measures that are more appropriate for epidemiological population studies that measure exposure and response to risk factors without controlling for confounding factors that could produce the same results from other sources.

Confounding factors are controlled in a vaccine clinical trial through randomization of participants to the vaccine and placebo groups, thereby equally distributing all known and unknown confounding factors. Randomized controlled clinical trials require absolute measures of risk reduction to prove causation of vaccine efficacy, not relative risk reductions that only observe associations of effectiveness. (Relative risk reduction: Misinformative measure in clinical trials and COVID-19 vaccine efficacy).

The absolute risk reduction of the COVID-19 vaccine clinical trials was approximately 1%, which rendered the vaccine clinically insignificant (Outcome Reporting Bias in COVID-19 mRNA Vaccine Clinical Trials). Generally, a significant clinical effect reduces a risk by at least 50% or increases a risk by at least two-fold.

In what amounts to the world’s longest natural experiment, it took many months for a national public health official to declare to the public what the clinical trial results had already proven back in 2020 due to their low absolute risk reductions: that the COVID-19 vaccines would not prevent SARS-CoV-2 infections (CDC Director Rochelle Walensky tells Wolf Blitzer that COVID Vaccines won't prevent transmission - YouTube 1:20).

And to suggest that the vaccines would at least keep you out of the hospital has never been clinically proven. Just because you are vaccinated and stay out of the hospital doesn't prove the vaccines had anything to do with it. It's just another one of those unproven associations.

By now the truth about the COVID-19 vaccine failure should be evident to anybody who cares to look and listen. However, are the lessons learned? Are we better equipped now to prevent more failed vaccine campaigns based on misleading statistics that benefit pharmaceutical profits? That last phrase provides a clue to the answer, and the world's longest natural experiment on vaccine efficacy is likely to continue on indefinitely.

https://www.trialsitenews.com/a/the-worlds-longest-natural-experiment-on-vaccine-efficacy-d9d9b7c3

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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)

http://jonjayray.com/blogall.html More blogs

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Long COVID damage can linger for 2 years, leading to elevated risk of disability, hospitalization, and death, landmark new study finds

Long COVID—and the increased risk of death, disability, and hospitalization it brings—can persist for two years, according to a landmark study published Monday in Nature Medicine.

It’s the first study to look at a broad range of potential health effects stemming from the virus in the two years after infection. Most previous studies had only examined the initial year after infection, or a more narrow range of health effects in a period slightly longer than a year.

For those who contracted the virus in 2020 and were hospitalized with it, the risk of both death and hospitalization remained “significantly elevated” for two years, according to researchers with the U.S. Department of Veterans Affairs and Washington University.

Among those who contracted the virus the same year and weren’t hospitalized during their initial infection, the risk of death remained statistically significant for six months, researchers found. The risk of hospitalization remained elevated for about a year and a half.

“The findings highlight the substantial cumulative burden of health loss due to [long COVID] and call for attention to the care needs of people with long-term health effects" due to the virus, the study’s authors wrote.

A longer road for those who were hospitalized

Researchers examined the Department of Veterans Affairs medical records of nearly 140,000 individuals who survived COVID during 2020, as well as nearly 6 million who weren’t known to have contracted the virus that year. They followed them for two years to gauge their risk of death from all causes, as well as the incidence of 80 conditions known to be post-acute sequelae of COVID (PASC), frequently referred to as long COVID.

At the two-year mark, the risk of most of those health conditions—69%—was insignificant for those who hadn’t been hospitalized with the virus. But "substantial" risk remained "impacting several major organ systems." The chance of developing blood, lung, gastrointestinal, or musculoskeletal conditions remained elevated, in addition to fatigue and diabetes, suggesting a longer-lasting risk for these ailments, the authors stated.

In a Monday blog entry, Dr. Eric Topol, a professor of molecular medicine at Scripps Research and founder and director of the Scripps Research Translational Institute, wrote that the statistic was the "only reassuring finding for non-hospitalized people in the study."

For those who had been hospitalized with the virus, the risk of most of conditions—65%, affecting all organ systems examined, and including cardiovascular, blood, endocrine, gastrointestinal, kidney, mental health, musculoskeletal, and pulmonary issues—remained significant for the entire two years. The findings are a nod to the "the difficult and protracted road to recovery among those whose disease was sufficiently severe to necessitate hospitalization during the acute phase of infection," researchers wrote.

The study's findings "show that while risks of many (but not all) post-acute sequelae decline and become non-statistically significant over time, the decline is less pronounced among those who were hospitalized in the acute phase of infection," the authors wrote.

The good news for everyone: Researchers found no increased risk of cancer among those who had experienced COVID, hospitalized or not.

While significant, the study had its limitations, as the authors point out. All participants were veterans, and most were older males. Long COVID as a whole may look different—in both duration and symptoms—in a primarily female, or younger, population. As Topol pointed out, the study's prototypic participant, a 61-year-old male, is far different from a female in her thirties—the demographic for which long COVID is thought to be most prevalent.

Further, all participants were infected during the first year of COVID, before variants like Delta and Omicron evolved. While thought to be less common, long COVID from later strains may feature important differences.

What's more, those with a record of COVID infection were compared to those with no record of a COVID infection during the same year. But some of them may have had COVID without knowing, or telling their doctor, skewing rates of death, hospitalization, and disability in the COVID crowd for better or worse.

Long COVID's long-term impacts on the immune system

Another new study, published Aug. 18 in the journal Cell, details the long-term immune system changes that severe COVID can trigger. The findings help elucidate why some with long COVID have symptoms tied to prolonged inflammation, like lung and kidney damage and neurological changes—and may have implications for anyone who has experienced the virus, regardless of severity.

Researchers with Weill Cornell Medicine in New York City and other institutions examined data from the blood of tens of patients—those who had recovered from severe COVID, and those who had recovered from other types of critical illness. In particular, they were able to isolate and analyze a rare type of stem cells found in blood—CD34+ hematopoietic stem and progenitor cells—thanks to a new technique they developed that made bone marrow biopsy unnecessary.

Among their findings: Monocytes—a type of white blood cell produced every few days from stem cells—showed changes in epigenetic programming up to a year after severe COVID infection.

Epigenetic programming refers to the epigenome—comprised of factors like chemicals, stress, diet, drugs, and disease that modify DNA, telling it "what to do, where to do it, and when to do it,” according to the U.S. National Institutes of Health. Those changes, to what could be casually referred to as DNA's "packaging," can be passed down from cell to cell as they divide, and from generation to generation.

Researchers also found that stem cells of those who had experienced severe COVID were more likely to allow activation of inflammation-associated genes. Such cells were also more likely to create a type of blood cell that serves as a "first responder" to infection.

Stem cells "can pass their epigenetic ‘memories’ on to their progeny immune cells, changing those cells’ inflammatory programs," Dr. Steven Josefowicz, an associate professor of pathology and laboratory medicine at Weill Cornell Medicine, told Fortune. "So, when they see another pathogen, they respond in a different way than they would if they came from ... cells that hadn’t seen inflammation to the same extent.”

Such changes to the immune system may persist longer than a year, Josefowicz said, adding that the study only lasted a year. And they may also occur—at least to some extent—in those who had more mild cases of COVID, though further study will be needed to tell.

Who's most at risk for long COVID?

Factors like age, gender, BMI, and pre-existing conditions may put individuals at higher risk for long COVID, according to a study published in March in the Journal of the American Medical Association Internal Medicine.

The U.K.-based study found that certain groups of people are at a significantly higher risk of developing the post-viral condition, thought to affect millions around the world. They include:

Women
Over 40
People with obesity
Smokers
Those who were immunosuppressed before COVID
People who were hospitalized with COVID
People who had the following conditions before COVID:

anxiety or depression
diabetes
asthma or COPD

Researchers examined the results of 41 published studies, with a combined total of more than 860,000 patients. They found that the aforementioned conditions were strongly associated with a higher risk of long COVID symptoms persisting three or more months after infection.

The results bolster the case that female gender and older age serve as risk factors for developing long COVID. A potential common thread among several risk categories: pre-existing inflammation, which may extend the acute phase of COVID “even after recovery.” In the case of females, hormones might play a role in inflammatory status, while obesity shares a proinflammatory profile with long COVID, the authors write.

That’s not-so-great news for a giant swath of the population. There is good news, however: At least two doses of COVID vaccination seemed to lower the risk of developing long COVID, researchers found. Other studies have come to similar conclusions, they noted. They include a report from the U.K. Office of National Statistics, which found that those with two doses of COVID vaccine had a 42% lower risk of developing the potentially disabling condition.

What is long COVID?

With more than 200 symptoms identified—from lingering cough and fatigue to ear numbness and a sensation of “brain on fire”—long COVID is undoubtedly not one but multiple conditions, experts say.

True long COVID, some contend, is best defined as a chronic-fatigue-syndrome-like condition that develops after a COVID infection, similar to other post-viral syndromes that can occur after an infection with herpes, Lyme disease, and Ebola, among others.

Other post-COVID complications like organ damage should not be defined as long COVID and better fit into the larger umbrella category of PASC, some experts say. Also known as post-acute sequelae of COVID-19, the term is used to encompass a wide variety of COVID consequences, from chronic-fatigue-like symptoms and subsequent heart disease to lasting lung damage and odd new symptoms like urinary incontinence, itching, and skin lesions.

As of Jan. 16, 15% of U.S. adults reported having long COVID symptoms at some point in the pandemic, and 6% reported lingering symptoms, according to a Jan. 26 report by the Kaiser Family Foundation, citing data from the U.S. Centers for Disease Control and Prevention.

The percent of Americans who’ve experienced COVID and still report long COVID symptoms dropped from 19% in June to 11% in January, according to the report.

https://fortune.com/well/2023/08/21/long-covid-last-2-years-death-disability-hospitalization/

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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)

http://jonjayray.com/blogall.html More blogs

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Health Break

No blogging from me today. Should be ok for tomorrow

Most Intensive Ivermectin Use Had 74 Percent Reduction in Excess Deaths

According to a new peer-reviewed ecological study, a natural experiment occurred when the government of Peru authorized ivermectin for use during the COVID-19 pandemic resulting in evidence of the drug’s effectiveness and ability to reduce excess deaths.

The paper’s results, published August 8 in Cureus, found a 74 percent reduction in excess deaths in 10 states with the most intensive ivermectin use over a 30-day period following peak deaths during the pandemic. When analyzing data across 25 states in Peru, researchers found these reductions in excess deaths correlated closely to ivermectin use during four months in 2020.

When ivermectin was available without restriction, there was a fourteenfold reduction in nationwide excess deaths. Once access to ivermectin was restricted by the government, a thirteenfold increase in excess deaths was observed in the two months following the limitation of its use. The findings align with summary data from the World Health Organization for the same time period in Peru.

Ivermectin is a widely-known and inexpensive treatment against parasitic diseases. Scientists believe the drug can also bind to the spike protein of the SARS-CoV-2 virus, limiting its morbidity and infectivity.

Peru Promoted Then Restricted Access to Ivermectin

Before Peru implemented COVID-19 vaccine mandates, the country relied on mitigation strategies such as lockdowns and therapeutics to control the SARS-CoV-2 virus that causes COVID-19, as did many other nations.

The Peruvian Ministry of Health, on May 8, 2020, approved ivermectin widely for use prompting 25 states in Peru to implement inpatient and outpatient treatments with ivermectin to different extents and in different time frames. Additionally, through the Mega-Operación Tayta (MOT)—a national program led by the Ministry of Defense—Peru’s government began distributing ivermectin on a wide scale.

Through a partnership with 11 other government agencies, MOT aimed to reach every targeted region with rapid response teams to detect COVID-19 cases, administer ivermectin, and provide food to encourage people to isolate for 15 days. Shortly thereafter, MOT began distributing the therapeutic to everyone identified as high-risk, regardless of whether they tested positive or were symptomatic for COVID-19.

The government of Peru independently tracked daily COVID-19 deaths and all-cause deaths through numerous Peruvian national health databases, allowing researchers to calculate excess deaths. Additionally, they extensively tracked data for deaths and other public health parameters allowing analysis of the potential efficacy of interventions such as ivermectin during the pandemic.

When President Francisco Sagasti took office on Nov. 17, 2020, the government stopped distributing ivermectin and made it available only by prescription. This made the drug significantly more difficult for people to obtain and allowed researchers to see nationwide changes in daily excess all-cause deaths before and after restrictions went into place.

Impact of Ivermectin on Excess Deaths

Excess all-cause deaths were calculated from the total deaths recorded for January through February 2020. During this period, monthly all-cause deaths fluctuated with a mean value of 5.2 percent and a standard deviation of 3.8 percent. By May 2020, total deaths fluctuated by more than double the baseline value calculated in January through February.

An analysis of excess all-cause deaths was performed state-by-state for those aged 60 years and older to establish the date of peak excess deaths during the pandemic’s first wave. Decreases in excess deaths from the peak date of death to 30 and 45 days afterward were tracked. The 25 states were then grouped by the extent of ivermectin distribution: maximal distribution—occurring through operation MOT, medium, and minimal.

Results showed that the 10 MOT states had a sharp decrease in excess deaths after reaching peak values—with a 74 percent drop at 30 days and an 86 percent drop at 45 days after the date of peak deaths. For 14 states that locally administered ivermectin, excess deaths dropped by 53 percent at 30 days and 70 percent at 45 days.

In Lima, where ivermectin treatments were delayed until August—four months after its initial pandemic surge in April—excess deaths only dropped by 25 percent at 30 days and 25 percent at 45 days after peak deaths on May 30.

According to the study, mean reductions in excess deaths 30 days after peak deaths were 74 percent, 53 percent, and 25 percent, respectively, for the maximal, medium, and minimal states that distributed ivermectin. Forty-five days after peak deaths, mean reductions were 86 percent, 70 percent, and 25 percent.

The researchers noted that ivermectin distribution may have yielded such positive numbers due to the drug’s ability to both prevent and treat COVID-19 when distributed to an at-risk population on a greater scale.

Similar Results Observed in Uttar Pradesh, India

Researchers noted similar results with ivermectin distribution in Uttar Pradesh, India, where government teams moved across 97,941 villages as part of a COVID-19 management program to distribute home medication kits that contained ivermectin, doxycycline, zinc, vitamins C and D3, and acetaminophen tablets.

After the mass distribution of ivermectin, the seven-day moving average of COVID-19 deaths in Uttar Pradesh decreased by 97 percent. The cumulative total of COVID-19 deaths per million in population from July 7, 2021, through April 1, 2023, was 4.3 in Uttar Pradesh, compared with 70.4 in all of India and 1,596.3 in the United States, according to the study.

Although Peru had more comprehensive data, the Uttar Pradesh data suggests using ivermectin may prevent and potentially treat COVID-19.

“These encouraging results from IVM [ivermectin] treatments in Peru and similar positive indications from Uttar Pradesh, India, which have populations of 33 million and 229 million, respectively, offer promising models for further mass deployments of IVM, as needs may arise, for both the treatment and prevention of COVID-19,” researchers concluded.

The authors considered factors that could influence their findings, such as the effects of a social isolation mandate imposed in May 2020, the varying genetic makeup of the SARS-CoV-2 virus, differences in seropositivity rates, and population densities across the 25 states. Still, researchers stated the extent and reliability of data showed other factors did not significantly influence study outcomes.

https://www.theepochtimes.com/health/most-intensive-ivermectin-use-had-74-percent-reduction-in-excess-deaths-in-peru-new-study-5470885

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Post-Vaccination Parsonage-Turner Syndrome: A Case Series

Cripes! I have something very like Parsonage-Turner Syndrome right at this moment: All sorts of painful symptoms in my right shoulder. And I have been Covid vaxxed. But the vax was years back and there is no associated muscle weakness so I suspect the resemblance is coincidental. I seem to be healing up anyway

Case reports on COVID-19 vaccination-related neurological events are appearing more frequently in the literature. TrialSite follows these case studies on adverse effects on the central and peripheral nervous system attributed to COVID-19 vaccines. The study summarized here describes six cases related to a rare neurological condition called “Parsonage-Turner syndrome (PTS)” that presented after COVID-19 vaccine shots.

Also called “brachial neuritis”, PTS is a neurological condition characterized by severe pain in the shoulder and upper arm followed by muscle weakness. It mainly affects motor nerves which are responsible for movement. These symptoms may last for months and are usually unilateral.

The condition is commonly seen in men as compared to women and although people of any age can develop the condition, the average age of onset is 41 years.

The study

The current case series published in Case Reports in Neurology in 2022 is entitled “Parsonage-Turner Syndrome Following COVID-19 Vaccination: Clinical and Electromyographic Findings in 6 Patients.”

Background

The reasons behind PTS are unclear, but reported causes include viral infections, surgery, vaccination, and trauma. One theory suggests that viral antigens in vaccines may trigger this syndrome. The condition is associated with various vaccines such as hepatitis B, diphtheria, pertussis, tetanus vaccine, smallpox, and swine flu.

The authors of the case report mentioned that during the first six months of 2021, a rise in PTS diagnoses was observed. A possible reason could be COVID-19 vaccination, so they investigated it further. They suggested that a mechanism behind PTS may be an immunization-induced inflammatory reaction against brachial plexus nerve fibers. Although rare, other case studies investigating the relationship between COVID-19 vaccines and PTS have been reported.

Methodology

A retrospective analysis was performed with six patients who had acute onset of pain and weakness in their upper extremities post vaccination. These patients were referred for electrodiagnostic (EDX) investigation for their reported symptoms. EDX investigations include electromyography (EMG) and nerve conduction studies and aim to identify the cause of pain. It evaluates muscle and muscle nerve health.

Along with EDX evaluation, patients’ clinical symptoms, physical exams, MRI findings, COVID-19 vaccination history, and treatments were discussed. Other potential underlying reasons for PTS were excluded.

Findings

Four patients had received the Pfizer-BioNTech vaccine while two patients had received Moderna. Symptoms had arisen around 17 days after the injection in either the same arm with the injection site (five patients) or the other arm (one patient). Two patients had received the first dose and four had received the second dose before the symptom onset. EDX evaluation revealed abnormalities and further confirmed the diagnosis of PTS with localization of the disorder to the brachial plexus.

To treat the condition, patients received prednisone/prednisolone, gabapentin, and physical therapy. All of the patients showed improvement in their arm pain in follow-up evaluations. While three did not show improvement in weakness, the other three’s symptoms of muscle weakness improved.

https://www.trialsitenews.com/a/post-vaccination-parsonage-turner-syndrome-a-case-series-236a3340

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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)

http://jonjayray.com/blogall.html More blogs

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When corrupted science becomes a threat to population health

‘The medical-political complex tends towards suppression of science to aggrandise and enrich those in power. And, as the powerful become more successful, richer, and further intoxicated with power, the inconvenient truths of science are suppressed. When good science is suppressed, people die.’ BMJ executive editor Kamran Abbasi

Below is a section from the Australian Medical Professionals Society’s (AMPS) submission to the Department of Infrastructure, Transport, Regional Development, Communications and the Arts Communications Legislation Amendment (Combating Misinformation and Disinformation) Bill 2023. The full submission can be viewed here. We encourage you to make a submission here by August 20.

AMPS believes granting ACMA, a government-appointed entity, the authority to label information contradicting official messaging as misinformation or disinformation establishes an alarming and precarious precedent. This becomes especially concerning considering the growing awareness of the effect of corporate conflicts of interest, leading to biased reporting within academia, biased media content, skewed therapeutic guidelines, and profit-driven public policies. History is replete with instances showcasing the consequences of authorities making decisions without being held accountable or having to be transparent about their actions. We must be cautious when policies, based on concealed health advice for instance, are determined by those in power without the requirement for empirical validation, effectively bestowing them the power to define what qualifies as true information.

The extensive sway exerted by pharmaceutical companies’ financial interests across medical academia and public policy presents a notable jeopardy to the credibility of healthcare and societal welfare. The involvement of pharmaceutical companies in financing research, regulation, education, and policy endeavours introduces an intrinsic susceptibility to bias, potentially undermining the impartiality of scientific investigation and policy development. This dynamic could result in an undue prioritisation of profit-centred incentives, overshadowing the imperative of prioritising patient well-being and the broader public health.

Professor Ioannidis describes what he calls a ‘misinformation mess’ where he claims much-published research is not reliable. Having to negotiate such a mess in deciding exactly what is misinformation offers no benefit to patients or decision-makers. It is a risk to public health.

The government must consider that many prominent journal editors have drawn attention to the pervasive influence of financial conflicts of interest on the reliability of research findings.

‘Financial conflicts can compromise the integrity of research,’ warns Dr. Fiona Godlee, editor-in-chief of The BMJ, stressing the potential bias that can result from industry funding.

Dr. Jerome Kassirer, former editor-in-chief of the New England Journal of Medicine, notes in his book, How medicine’s complicity with big business can endanger your health, the ‘shocking extent of these financial enticements and explains how they encourage bias, promote dangerously misleading medical information, raise the cost of medical care, and breed distrust’, highlighting the distortion such conflicts can introduce into the scientific record.

Dr. Virginia Barbour, founding editor of PLOS Medicine, adds, disclosure alone is insufficient to address conflicts, emphasising the need for greater transparency and safeguards against undue influence.

Dr Maria Angell, long-time editor in chief of the NEJM resigned more than 20 years ago after 20 years as editor because of what she described as the rising influence of the Pharmaceutical industry. She said in her book, The truth about drug companies: How they deceive us and what to do about it, ‘Now primarily a marketing machine to sell drugs of dubious benefit, big pharma uses it wealth and power to co-opt every institution that might stand in its way, including the US congress, the FDA, academic medical centres and the medical profession itself.’

These editorial voices collectively emphasise the imperative of robust disclosure mechanisms and stringent evaluation of financial conflicts to maintain the integrity and credibility of research in the face of commercial interests.

AMPS would argue that the demonisation of Ivermectin during the pandemic is a prime example of how financial conflicts of interests that claimed extensive evidence demonstrating the effectiveness of Ivermectin in the treatment and prevention of Covid resulted in harm.

Our submission to the TGA’s rescheduling of Ivermectin showed how statistically significant the evidence base is to support the clinical improvements in time to clinical recovery, time to viral clearance, and reduction in hospitalisation and death from this cheap, safe, fully approved, WHO essential medicine. This medication was banned by the TGA claiming safety and efficacy concerns when their own 2013 Australian Public Assessment Reports (AusPAR) demonstrated safety and instead recommended for example the use of provisionally approved very expensive Remdesivir. Remdesivir in the WHO Solidarity Trial reported in the NEJM was found to have ‘little or no effect on hospitalised patients with Covid, as indicated by overall mortality, initiation of ventilation, and duration of hospital stay’. In fact, in 2020 the WHO recommended against the use of Remdesivir in Covid patients. A study in the Lancet from September 2021 found, ‘No clinical benefit was observed from the use of Remdesivir in patients who were admitted to hospital for Covid, were symptomatic for more than 7 days, and required oxygen support.’ The banning of Ivermectin in favour of antivirals such as Remdesivir appears to make little evidentiary or clinical sense.

Dr Mike Magee, former physician spokesman for Pfizer, published in 2019 his book Code Blue: Inside America’s Medical Industrial Complex. He powerfully describes the corruption of the US healthcare system.

‘Cosy relationships and generous gratuities have demonstrated a remarkable ability to corrupt even those we would instinctively put on the side of the angels, including members of the biomedical research community, deans of medical schools, directors of continuing medical education programs, officers at the NIH and FDA, and even seemingly altruistic patient advocacy organisations like the American Cancer Society.’

AMPS has also written quite extensively about our concerns regarding the conflict between the government safety and efficacy claims for the Covid vaccinations and the lack of comprehensive safety and efficacy data surrounding these novel immunisations. While the accelerated development and emergency approvals were perhaps motivated by the global health crisis, some experts caution that the available data are not yet as extensive as in standard vaccine development processes.

AMPS has written about our concerns with these vaccines especially for children. According to our Therapeutic Goods Administration (TGA) AusPAR long-term safety data remains a critical gap in our understanding, emphasising the importance of continued post-vaccination pharmacovigilance. Dr. Peter Doshi, an associate editor at The BMJ, underscores the need for transparent and thorough reporting of clinical trial results to ensure the public’s confidence in these vaccines.

Financial conflicts of interest can erode trust in medical research, undermine the credibility of academic institutions, restrict access to transparent data, and ultimately result in the promotion of treatments or policies that prioritise corporate gain over the impartial pursuit of knowledge and the advancement of public welfare. Stricter safeguards and transparency measures are essential to mitigate these dangers and ensure that medical academia and public policy remain steadfastly committed to unbiased and evidence-based decision-making when seeking to define what constitutes mis-or-disinformation.

We should heed Abbasi’s warning before science itself becomes a threat to overall population health, or maybe we are too late.

‘Science is being suppressed for political and financial gain. Covid has unleashed state corruption on a grand scale, and it is harmful to public health. Politicians and industry are responsible for this opportunistic embezzlement. So too are scientists and health experts. The pandemic has revealed how the medical-political complex can be manipulated in an emergency — a time when it is even more important to safeguard science…’

https://www.spectator.com.au/2023/08/when-science-becomes-a-threat-to-population-health

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For the COVID-19 Vaccine Injured: Time for Action

A recent letter to the editor of the Peninsula Daily News, a local press serving the Olympic Peninsula in Washington State shares some possible good news for persons struggling with injuries associated with the COVID-19 vaccines. Could real change be around the corner with the proposed bipartisan Vaccine Injury Compensation Act?

A local resident, Kathy Zelenka seeks to influence the area’s politicians to ensure they support the legislation. Why? Because “politicians need to hear that their constituents care.”

The Port Angeles, Washington State resident summarizes the challenge well: “To live in a world where people harmed by a medication are treated with mercy instead of censorship, people must make their voices heard.”

Reaching into the dark past of Germany during WW2, Zelenka cites a quote from Dietrich Bonhoeffer, a Lutheran pastor, theologian and anti-Nazi dissident who is known to have said, “Not to speak is to speak. Not to act is to act.”

Ms. Zelenka educates her local politicians Derek Kilmer and Patty Murray on the new Office of Long COVID Research and Practice launched by the Biden administration and recently reported on by TrialSite. Importantly, she urges local residents to press the politicians to add vaccine injury studies to that new office, or conversely, set up an equivalent office.

She suggests the politicians read “Insult to the Injured: The Case for Modernizing Vaccine Injury Compensation” a recent piece published in Health Affairs co-authored by an advisor to vaccine makers and the director of Vaccine Injury Litigation at George Washington University Law School.

The opinion writer rightly points out that “we need each other.”

React19 is supporting this vaccine injury compensation reform. The largest COVID-19 vaccine injured group in the United States, if not the world, shared some thoughts on the proposed bipartisan legislation.

The organization, which collaborates with TrialSite, is identified as a science-based non-profit offering financial, physical and emotional support for those suffering from long-term COVID-19 vaccine adverse events globally.

Serving React19 as Legal Affairs Director, Christopher A. Dreisbach told TrialSite via email that “in an ideal world the COVID-19 vaccine-injured would be able to hold the pharmaceutical industry directly accountable through personal injury actions. Nonetheless, this bill represents the next best thing.”

As TrialSite has reported, the current COVID-19 vaccine injured population must navigate the completely broken Countermeasures Injury Compensation Program (CICP). The proposed legislation among other things would move the COVID-19 vaccine injured to the at least somewhat functional Vaccine Injury Compensation Program.

According to React19’s counsel:

“By transitioning the COVID-19 vaccines to the VICP, this bill represents the comprehensive reform the vaccine-injured desperately deserve. We commend Representative Doggett and Representative Smucker for their bipartisan effort - an unfortunately rare occurrence in today’s highly polarized political environment.”

React19 has a message for politicians that might try to water down, dilute the proposed legislation:

“Incremental CICP reforms, proposed by other lawmakers, will not make a meaningful difference to the COVID-19 vaccine-injured. That program is simply too broken to fix. This bill is a welcome departure from such a short-cited approach.”

Given that over 230 million people are now considered fully vaccinated, TrialSite estimates that anywhere from half-a-million to just over 2 million people are in dire need of care, suffering with life changing injuries caused by the COVID-19 vaccines.

Many of these people are barely getting by, and the medical establishment hasn’t embraced vaccine injures as key opinion leaders in the National Institutes of Health, Food and Drug Administration and Centers for Disease Control and Prevention have yet to step forward and open up the dialogue publicly.

It’s time they do so.

https://www.trialsitenews.com/a/for-the-covid-19-vaccine-injured-time-for-action-26b77ba5

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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)

http://jonjayray.com/blogall.html More blogs

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