Meta-Analyses of School Closures by University of Oxford

New research out of the United Kingdom points to heightened levels of harm associated with COVID-19 lockdowns and school closures, with an emphasis on the particularly adverse impacts of the latter. Led by Professor Kamal R. Mahtani, and colleagues at University of Oxford, the findings were telling. After a systematic review, the team had their findings published in the British Medical Journal drilling into the actual positive and negative impacts of school closures. The team finds a lot of problems with school closures (mental health, learning, etc.) as well as some positive outcomes (reduce transmission, etc.). But in-school mitigation also can help. The quality of the evidence associated with the underlying systematic reviews was low to very low. The point here is that with any pandemic, evidence-based approaches should be taken, not just what public health authorities decide on a whim.

Employing use of a critical appraisal tool for systematic reviews that include both randomized and non-randomized studies involving healthcare interventions (or both) called AMSTAR 2, the UK-based researchers sought to evaluate confidence in the included systematic reviews. They also used GRADE to assess the certainty of evidence associated with the studies looking into the impacts of school lockdowns. GRADE, or “Grading of Recommendations, Assessment, Development, and Evaluations,” is a transparent framework for developing and presenting summaries of evidence, thus contributing to a more systematic approach for making clinical practice recommendations.

Key study questions pursued by the Oxford-based investigators included:

(1) What is the impact of school closures on COVID-19 transmission, morbidity or mortality in the community?

(2) What is the impact of COVID-19 school closures on mental health (e.g., anxiety), physical health (e.g., obesity, domestic violence, sleep) and learning/achievement of primary and secondary pupils?

(3) What is the impact of mitigations in schools on COVID-19 transmission, morbidity or mortality in the community?

(4) What is the impact of COVID-19 mitigations in schools on mental health, physical health and learning/achievement of primary and secondary pupils?

The findings

Out of 578 reports, the team included only 26 based on the application of rigorous inclusion/exclusion criteria.

In this study, the team identified a total of 132 unique primary studies involving the effects of school closures on transmission of COVID, morbidity and mortality; 123 on learning; 164 on mental health, 22 on physical health; 16 on sleep with 7 concerning domestic violence. Finally, 69 of the individual studies focused on the effects of in-school mitigations on transmission/morbidity/mortality report the study authors.

The authors communicate in The BMJ:

“Both school closures and in-school mitigations were associated with reduced COVID-19 transmission, morbidity and mortality in the community. School closures were also associated with reduced learning, increased anxiety and increased obesity in pupils. We found no SRs that assessed potential drawbacks of in-school mitigations on pupils. The certainty of evidence according to GRADE was mostly very low.”

Overall, the Oxford academic researchers considered the whole body of evidence as weak when considered holistically. However, this doesn’t take away from numerous concerns in the form of negative effects on children involving school closures.

The study authors concluded that while school closures lead to both positive and negative impacts, the overall level of evidence confidence is mostly very low. Importantly they could not find any systematic reviews investigating the potential drawbacks of in-school mitigations on children, which should be studied.

https://www.trialsitenews.com/a/meta-analyses-of-school-closures-by-university-of-oxford-f92697a8

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Singapore Academic Medical Research Climate Healthier and More Open Than America: At Least When It Comes to COVID-19 mRNA Vaccines

While Singapore is known as somewhat of an authoritarian place, albeit free and relatively open for business and some labor, when it comes to an open discussion about the problem of COVID-19 vaccine injuries, its press is far more open and freer than that of the United States. Two well-known COVID-19 researchers, part of elite Singapore-based academic medical centers, bring real talk to the COVID-19 vaccine topic. They want to see highly efficacious vaccines that have less side effects—implicitly acknowledging problems with the current mRNA-based products. Delving into the risk-benefit analyses, they are free to speak their mind in Singapore, while Americans peers generally cower in economic fear. Some commonsense talks now come out of Singapore, the type that is sadly lacking in most top American academic medical/research circles.

During the COVID-19 pandemic, the City-State implemented “circuit breakers and lockdowns” in a bid to control the spread of the pandemic—much like other Asian nations and even Australia—they also implemented mass vaccination schemes to reduce the risk of severe symptomatic COVID, also part of the quest to transition out of the pandemic. Of course, the scale and magnitude of the mass vaccination program was but a fraction of the effort in the United States, given that over 270 million people in America received their primary series vaccination out of a population of 330 million.

Singapore, with its population at 5.5 million, through a combination of mandates and incentives, saw over 92% of the City-State’s population vaccinated against COVID-19. By the late summer of 2021, they were classified by the German press as the world’s most vaccinated place against COVID-19.

The press there have been open about two tragic deaths associated with the COVID-19 vaccines. As reported by the Singapore news outlet CNA and covered by TrialSite as well, a 43-year-old Filipino woman died just four days after vaccination with the Pfizer-BioNTech mRNA jab (BNT162b2), while at the end of 2021, a 28-year-old Bangladeshi man died three weeks after the first dose of the mRNA-based Moderna COVID-19 vaccine known as mRNA-1273 or Spikevax.

In a commentary from Ooi Eng Eong of Duke-NUS Medical School, and Paul Ananth from NUS Yong Loo Lin School of Medicine, they point out that:

“There is no vaccine or medication in the world without the risk of rare severe adverse events, so their use must always be guided by risk-benefit analyses.”

It’s interesting, the timing and topic of this opinion piece in the prominent Singapore multi-channel media. This isn’t the fringe, some politically charged platform, but rather the mainstream in the heart of a very orthodox and mainstream place at this point .

While both Drs Eong and Ananth remind all that a known potentially dangerous side effect associated with the mRNA COVID-19 vaccines—myocarditis, can also occur directly as a result of SARS-CoV-2 infection, the two absolutely mainstream medical research professionals remind us of all to learn from both smallpox and poliomyelitis.

With a refresher on the history of these vaccines, and a reminder that on very rare occasions risks of serious side effects can and do occur. In fact, in Singapore, the risks associated with the vaccine became unacceptably high:

“With poliomyelitis having been eliminated in most parts of the world, the risk of vaccine-associated paralysis became unacceptably high. Singapore, like many countries, has switched fully to the injected form, which is composed of killed polioviruses and has no risk of paralysis.”

Overall, the Singapore-based academic medical researchers are pleased with the COVID-19 vaccination outcomes, but they believe more can be done to make these and other vaccines even safer.

Arguing that unfortunately, COVID-19 won’t be the least pandemic likely in the next decades, they point out that “in just the first 23 years of the 21st century, the world has witnessed nine major outbreaks that spread rapidly across national borders.” So obviously, they point out, “For public health authorities, the next pandemic is not a question of “if” but “when.”

What’s recommended?
While Ooi Eng Eong and Paul Ananth don’t go too far in the critique—this wouldn’t be publishable—they do hint that perhaps, the COVID-19 vaccines were expedited a bit too fast. For example, the two note, “For any vaccine to be licensed, including the COVID-19 vaccines developed in record time, it will have to be tested in preclinical animal models as well as tens of thousands of human volunteers for safety and efficacy.”

Importantly, both Pfizer-BioNTech and Moderna’s mRNA vaccines included some limited animal research and Phase 3 trials with 30,000+ participants.

TrialSite has access to numerous data, documents and testimony that these studies were overly rushed, with glaring problems that were covered up. Accessing some of the documentation in the Brook Jackson lawsuit (now dismissed), it’s clear that one major investigator site network’s quality track record was unacceptable, and in normal times this alone would have paused the clinical trial.

Other findings from the disclosed Pfizer regulatory documentation (See Sonia Elijah articles) or how the company cut some corners not conducting any controlled IND-enabling preclinical studies are further glaring examples that the compressed research during the pandemic was far from optimal.

Both Eong and Ananth know this, but of course, cannot articulate such points in mainstream media or for that matter, in their respected academic medical departments.

But they both do emphasize the importance of safety for any licensed medicinal products, including vaccines, noting that “Vaccines that produce side effects that are not well tolerated will fail clinical development and will not be marketed.” They continued pointing to the current situation with Pfizer and Moderna:

“However, despite clinical trials involving tens of thousands of volunteers, rare side effects that occur in the region of 1 in 100,000 vaccinations or less will likely be missed for simple statistical reasons.”

Yet they pair point out that clinical trials programs needing hundreds of thousands of volunteers just would not be viable.

Instead, the two Singapore-based COVID-19 experts point out that the key is to better understand what’s causing vaccine side effects. Why? “So that we can reduce them while maintaining the benefits of vaccination.”

Critically important, Eong and Ananth point out the logic that seemed so apparent in America—that “side effects do not indicate and are not required for good immunity, contrary to some popular views.”

Their point is that according to their research, “Vaccinated individuals who experience side effects do not develop better or higher levels of protection against COVID-19 than those who do not.”

Those healthy clinical trials volunteers with a healthier immune system during vaccination would be more likely to experience mild COVID-19 after mRNA vaccination. Yet an “Over-activation of a specific gene and low-level chronic inflammation contributed to the development of cardiac complication after booster COVID-19 mRNA vaccination,” the authors report in their research published in Cell Press journal.

They point to the need for the development of a “a detailed map of the molecular processes that lead to side effects and rare severe adverse events will lay the foundation for the development of safer vaccines, including potentially for the next emerging infectious disease.”

With ongoing research, the authors point out in their CNA editorial what are the next steps to both building protection via vaccination, while improving pandemic control hopefully done in a more responsible way.

Some common sense talks out of Singapore, the type that is sadly lacking in most top American academic medical/research circles.

https://www.trialsitenews.com/a/singapore-academic-medical-research-climate-healthier-and-more-open-than-america-at-least-when-it-comes-to-covid-19-mrna-vaccines-9109fe16

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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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Texas Attorney General to Investigate Whether COVID-19 Vaccine Makers Misled Public

The highest-ranking prosecutor in Texas is launching an investigation into whether the three top COVID-19 vaccine manufacturers have misled the public.

Texas Attorney General Ken Paxton is probing whether Moderna, Pfizer, and Johnson & Johnson misrepresented the efficacy of their COVID-19 vaccines, the Republican announced on May 1.

The companies may have violated the Texas Deceptive Trade Practices Act, Paxton said. That state law bars people from disseminating a statement that they know “materially misrepresents the cost or character of tangible personal property, a security, service, or anything he may offer” for the purpose of selling a product or service.

It also prohibits representing that goods are “of a particular standard, quality, or grade … if they are of another.”

Most of the COVID-19 vaccine doses administered in the United States have been manufactured by Moderna or Pfizer and its partner, BioNTech, according to federal data. Johnson & Johnson’s vaccine has been the third most popular in the country. No other vaccines were available until 2022.

Also at issue is whether the companies engaged in research to make a virus or pathogen more dangerous by increasing its transmissibility or pathogenicity and misleading the public about doing so.

Paxton sent civil investigative materials to all three companies that demand the production of documents and information within 30 days, including whistleblower reports and concerns regarding COVID-19 vaccine trials.

The materials also demand documents showing the rates of side effects for each vaccine and when the companies became aware of “unexpected or additional adverse events, side effects, injuries and/or deaths” related to their COVID-19 vaccines.

The companies also were told to hand over documents showing all investigations that were opened by federal, state, county, and local agencies, including law enforcement officials, related to representations made about the safety and effectiveness of the shows.

“The development of the Covid-19 vaccine, and the representations made by and knowledge of Pfizer, Moderna, and Johnson & Johnson, are of profound interest to the public’s health and welfare. This investigation aims to discover the truth,” Paxton said in a statement.

“This pandemic was a deeply challenging time for Americans. If any company illegally took advantage of consumers during this period or compromised people’s safety to increase their profits, they will be held responsible. If public health policy was developed on the basis of flawed or misleading research, the public must know. The catastrophic effects of the pandemic and subsequent interventions forced on our country and citizens deserve intense scrutiny, and we are pursuing any hint of wrongdoing to the fullest.”

While the manufacturers are largely shielded from lawsuits because of the Trump administration’s Public Readiness and Emergency Preparedness Act in 2020, there’s an exception for actions or failures to act that constitute “willful misconduct.” That’s an act or omission that’s taken “intentionally to achieve a wrongful purpose,” “knowingly without legal or factual justification,” and “in disregard of a known or obvious risk that is so great as to make it highly probable that the harm will outweigh the benefit.”

While being recorded without his knowledge, a senior Pfizer employee said in video footage released in January that Pfizer was aiming to “preemptively develop new vaccines” by mutating COVID-19.

“If we’re going to do that though, there’s a risk of like, as you could imagine—no one wants to be having a pharma company mutating [expletive] viruses,” Dr. Jordon Walker, a director of research and development at Pfizer, told nonprofit Project Veritas.

He said scientists at Pfizer were “optimizing” a process to mutate COVID-19 but were going slow “because everyone is very cautious.”

Pfizer later acknowledged that it had been conducting experiments that involved using the original COVID-19 virus “to express the spike protein from new variants of concern.”

“This work is undertaken once a new variant of concern has been identified by public health authorities,” the company stated. “This research provides a way for us to rapidly assess the ability of an existing vaccine to induce antibodies that neutralize a newly identified variant of concern. We then make this data available through peer reviewed scientific journals and use it as one of the steps to determine whether a vaccine update is required.”

Dr. Robert Malone, who helped develop the messenger RNA technology on which Pfizer’s vaccine is based, said that the experiments Pfizer described met the definition of gain of function.

“What they’re describing is almost identical to what was apparently done at the Wuhan Institute of Virology”—the laboratory from which some experts believe that COVID-19 escaped—Malone told NTD.

The Chinese laboratory was conducting risky experiments on mice, U.S. authorities have said, and is located in the same city where the first COVID-19 cases were detected.

Walker used the term “directed evolution” while speaking to Project Veritas, which Malone said is so similar to gain of function as to be irrelevant.

Paxton’s civil demand requests all communications and documents related to Pfizer engaging in either gain of function or directed evolution “in the study, analysis, trials, or preparation of the COVID-19 vaccine.” The same demand was made to Moderna and Johnson & Johnson.

https://www.theepochtimes.com/texas-prosecutor-investigating-whether-covid-19-vaccine-manufacturers-misled-public_5233338.html

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CDC Eases COVID-19 Vaccination Requirements for Foreign Travelers

A single dose of the most widely utilized COVID-19 vaccines is sufficient for international travelers to meet the requirements to enter the United States, the U.S. Centers for Disease Control and Prevention (CDC) said in an update.

Foreign travelers who receive a single dose of the Pfizer or Moderna vaccines meet the requirements, according to the CDC.

“Because some traveler vaccine records might not specify whether recent Moderna or Pfizer doses received were bivalent, CDC will consider anybody with a record of a single dose of Moderna or Pfizer vaccine issued on or after August 16, 2022, to meet the requirements of the Amended Order to board a plane to the United States,” the CDC website reads.

The bivalent vaccines from Moderna and Pfizer were first introduced in the United States as boosters in the fall of 2022. They’re now available as a one-dose primary series for most Americans, replacing the old vaccines. The CDC does recommend that some people get an updated shot as a booster even if they already received one, despite fleeting protection against hospitalization and poor shielding against infection.

The United States has required noncitizen nonimmigrants to provide proof of COVID-19 vaccination since 2021, under a proclamation issued by President Joe Biden. Exceptions are given for certain reasons. No religious exceptions are accepted.

The vaccination requirements state that a traveler arriving by air must be fully vaccinated, defined as two weeks after receiving a dose of an accepted single-dose vaccine or the second dose of an accepted two-dose series.

The CDC previously required two doses of the Moderna or Pfizer vaccines to meet the requirements. A single dose of the Moderna or Pfizer vaccines is now acceptable, alongside a single dose of the Johnson & Johnson vaccine, available in the United States and elsewhere, or a single dose of the Convidecia vaccine, which isn’t available in the United States.

Two-dose vaccines include Novavax’s vaccine, available in the United States; AstraZeneca’s vaccine, available in Europe and some other countries; and Sinopharm, a Chinese vaccine. People who received a two-dose series of the old Moderna or Pfizer vaccines can still travel to the United States.

To present proof of vaccination, a person must show a digital or paper record such as a vaccination certificate from the European Union.

The United States is one of a small number of nations that still require proof of vaccination to enter the country.

It’s not clear whether the foreigner vaccination requirements will remain in place beyond May 11, when the U.S. public health emergency over COVID-19 is set to expire. The COVID-19 national emergency was already rescinded after Biden signed legislation that was approved by Congress.

https://www.theepochtimes.com/cdc-eases-covid-19-vaccination-requirements-for-foreign-travelers_5230702.html

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Washington Post Editorial Points to Covid Vaccine’s Disruption of Women’s Menstrual Cycle

In a recent editorial in the Washington Post, Kate Clancy, a biological anthropologist and professor at the University of Illinois, wrote about how after she received her first dose of the Covid vaccine she got her period and the bleeding was so heavy she “was swapping out overnight-strength pads every hour.”

Clancy tweeted out her experience and expected a response of only about 500 people. Instead, she heard from 165,000. The responses spoke volumes. After the vaccinations women had changes in their periods. “Changes in menstruation were uncomfortable and often painful, people reported. Strangers described bleeding through their clothes at work.

Postmenopausal people were terrified they had cancer.” What seemed to surprise Clancy the most was the response of the medical community. “It is medical scientists’ duty to predict, look for and, if found, disclose side effects — and here is where I believe some in the medical community fell short.” In fact, Clancy cites medical authorities who claim excessive bleeding after Covid vaccination was a result of ‘pandemic stress”. Dr. Melissa Viray, Deputy Director for the Richmond City and Henrico County Health Districts doesn’t believe there’s a physiologic link between the vaccine and a woman's menstrual cycle, and would not classify it as a side effect of the Covid vaccine. “That’s just not how these vaccines work -- so I’d be very surprised," said Dr. Viray.

However, Viray did concede the Covid vaccine puts stress on the body. "Any time you put a stressor on the body, there are definitely -- there are definite changes that occur," Dr. Viray said. "...I could see where it might have, it might influence menstrual cycles in a little way, but just in the way that any stressor or any change to the environment for some individuals can change their menstrual cycles."

Medical Community “Fell Short”

According to Clancy, there is no question the vaccine saved lives. TrialSite has concurred with this point of view, although the products first rapidly authorized after less than a year of clinical development did come with rare side effects that may not seem so rare given that over 270 million people in America alone received the primary vaccination dose.

Clancy points out “clinical trials of the coronavirus vaccines did not ask questions about menstruation beyond inquiring about date of last menstrual period at the start of the study, to ensure participants were not pregnant. A participant in one of the trials emailed me to say it took two tries to persuade her trial site to include anything in her chart about her menstrual changes — the first time, they refused on the grounds that she was probably just perimenopausal.” In September of last year the National Institutes of Health (NIH) released an article about a study which confirmed a link between the Covid-19 vaccination and an increase in a woman’s menstrual cycle.

However, the NIH report claimed the increase in length, post Covid vaccine, was temporary. The study didn’t answer all the questions women had about the corona vaccine and the connections to women’s periods. Specifically, that the vaccine can make a woman’s period worse. But Clancy raises a bigger problem.

‘Menstrual changes matter to millions of people, and pharmaceutical companies, medical professionals and politicians need to invest in research and provide incentives for redesigning research so that it accommodates menstruation. Medical treatments and vaccine trials — for coronavirus and other maladies — will continue to disserve those bodily systems about which they ask no questions. We deserve better than to be surprised when a new treatment makes us bleed on our office chair.”

https://www.trialsitenews.com/a/washington-post-editorial-points-to-covid-vaccines-disruption-of-womens-menstrual-cycle-shortcomings-of-the-medical-establishment-dceaa271

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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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US Officials Reject Compensation for People Diagnosed With COVID-19 Vaccine Injuries

U.S. authorities rejected multiple people who sought compensation for COVID-19 vaccine injuries, despite diagnoses from doctors, documents show.

Letters from U.S. officials reviewed by The Epoch Times show officials contradicting doctors who treated patients as they turned down requests for payment.

Cody Flint, an agricultural pilot, was diagnosed by four doctors with a severe adverse reaction to Pfizer’s COVID-19 vaccine. Shortly after being vaccinated, Flint experienced intense head pressure, which led to problems such as perilymphatic fistula, the doctors said.

Flint sent a slew of medical files, including evidence of the diagnoses, to the U.S. Countermeasures Injury Compensation Program (CICP), which compensates people who prove they were injured by a COVID-19 shot.

But administrators for the program rejected Flint’s application in a denial letter, saying they “did not find the requisite evidence that the Pfizer COVID-19 vaccination caused” the conditions from which he suffers.

Flint, in his 30s, felt his first symptoms within an hour of vaccination. An onslaught of severe symptoms followed while he was flying two days later.

“One second I went from having burning in the back of my neck and tunnel vision to the very next second I was slumped over in my airplane. The best way I know to describe it, it was like a bomb went off inside my head,” Flint said.

CICP administrators told him that “compelling, reliable and valid medical and scientific evidence does not support a causal association between the Pfizer COVID-19 vaccine and benign paroxysmal positional vertigo, perilymphatic fistulas, increased intracranial pressure, Eustachian tube dysfunction, hearing loss, or loss of eyesight.”

They also tried to pin the problems on barotrauma. Colloquially known as airplane ear, barotrauma happens when air pressure suddenly changes, and is common as planes climb higher in the sky. Barotrauma causes the fistulas and symptoms of the fistulas “began while flying,” administrators wrote.

Flint and his doctors asserted in appeal letters that the barotrauma theory doesn’t hold up because Flint flies low as he dusts crops. Flint’s condition is “not from barotrauma,” Flint’s doctors told the CICP. “As an agricultural pilot, he does not fly more than a couple of hundred feet off the ground which is not of a magnitude to where he is at risk for barotrauma.”

“Elevated intracranial pressure has been recognized as a complication of COVID vaccination, and given the sequence of events, more probable than not, it is the cause of Mr. Flint’s elevated intracranial pressure, which had been documented on lumbar puncture,” they added. “The elevated intracranial pressure led to his perilymphatic fistula. Elevated intracranial pressure is a cause for perilymphatic fistula and more probable.”

The CICP determination was reviewed by a panel that sided with administrators. The panel found that the COVID-19 vaccine “did not cause Mr. Flint to develop bilateral perlympathic fistulas and related symptoms,” Suma Nair, an administrator, told Flint in a final denial letter. “There is no compelling causal connection between the Pfizer COVID-19 vaccine and the symptomology Mr. Flint experienced; the more likely cause of Mr. Flint’s symptoms is trauma from flying a plane, which would have developed over time.”

Administrators cited no studies or other evidence in their letters.

Flint said that the determination was wrong, pointing to a number of papers detailing post-vaccination intracranial and other neurological issues. He also noted a study that said intracranial pressure can cause perilymphatic fistulas.

Nair also said the panel concluded: “given the timeline of symptoms, it was not plausible for the Pfizer COVID-19 vaccine to have caused the otologic and vestibular issues experienced by Mr. Flint.”

“It’s just all comical to me,” Flint told The Epoch Times. “I get the shot, I’m injured within 48 hours, and they say that that makes it implausible.”

Difficulty Getting Compensation

The case highlights how people who experienced problems after vaccination have struggled to get money from the federal government, even when doctors diagnose vaccine injuries.

Flint is one of 76 people who were rejected as of April 1 because administrators determined they did not “show that a covered serious physical injury was sustained as the direct result of the administration” of a COVID-19 vaccine.

“The CICP may only make such determinations based on compelling, reliable, valid, medical and scientific evidence,” the program says.

More than 8,100 applications, as of April 1, have been submitted to the CICP for compensation for a COVID-19 vaccine-induced injury or death. Three hundred and sixty-two in total have been turned down. Just 23 have been accepted. All but two are for a type of heart inflammation called myocarditis or a related condition known as pericarditis, both of which U.S. authorities say are caused by COVID-19 vaccination.

Documents on the denials and acceptances have been largely withheld from the public. Freedom of Information Act (FOIA) requests, successful in unearthing information about COVID-19 vaccine safety, have yielded few documents. Administrators located 652 records in response to one request seeking all claims and associated documents. They only released 52 heavily redacted documents, citing exceptions to FOIA. A similar request returned a single page that wasn’t already public.

COVID-19 vaccine injuries fall under the CICP, a little-used program before the pandemic that was created by Congress in a 2005 bill, because of a Public Readiness and Emergency Preparedness Act declaration entered during the Trump administration that has not yet been rescinded.

Most administered vaccines in the United States fall under the National Vaccine Injury Compensation Program, enabling people with alleged or actual injuries to take their cases to federal judges in a no-fault system that paid out $4.8 billion between 1988 and 2022.

Decisions on CICP petitions, in contrast, are decided by the Department of Health and Human Services (HHS) Health Resources and Services Administration (HRSA)—the same agency that operates the program.

That “potentially creates a conflict of interest,” researchers wrote in a 2022 paper, advising Congress to initiate major reforms by either relocating the program or allowing judicial review of determinations.

Some members, including Sens. Cindy-Hyde Smith (R-Miss.) and Ron Johnson (R-Wis.) have expressed interest in reform but no bills have gained traction yet in the divided Congress.

People who apply to the CICP are only eligible for money for unreimbursed medical expenses and lost pay. Survivors of people who die can get death benefits. The National Vaccine Injury Compensation Program covers past and future healthcare costs, pain and suffering, lost earnings, and legal fees.

The CICP has paid just $6 million to date, including under $5,000 total to the only three people who were injured by COVID-19 vaccines and have been compensated.

‘All These People Are Going to Get Denied’

Dr. Joel Wallskog was one of the first people to receive Moderna’s COVID-19 vaccine. He got a shot on Dec. 30, 2020. Within days, he experienced symptoms including a loss of balance, headaches, and leg weakness.

“I was completely healthy, very active,” Wallskog, 53, told The Epoch Times. “Now I take 20 medicines.”

Wallskog was diagnosed with transverse myelitis, or spinal cord inflammation. At least two doctors have concluded the injury was caused by the vaccine, records show.

Wallskog transmitted medical records and supplementary documents, such as a study from National Institutes of Health researchers that discussed reports of neuropathic symptoms following COVID-19 vaccination. The same researchers diagnosed multiple people with vaccine injuries.

CICP administrators rejected Wallskog’s petition.

“The current medical and scientific evidence does not show a causal link between the Moderna COVID-19 vaccine and transverse myelitis, other neuro-inflammatory disorders, myelopathy, or thrombotic disorders, including spinal cord infarction,” Dr. George Reed Grimes, director of the HRSA’s Division of Injury Compensation Programs, wrote in the denial letter.

“Furthermore, there is no evidence that your symptoms of lower extremity numbness and tingling with neck flexion, and chronic thoracic pain with weakness and numbness in your legs, is caused by the Moderna COVID-19 vaccine,” he added.

Administrators did not note the doctors’ diagnoses or cite any studies.

One doctor had written in office notes that Wallskog suffered a “significant reaction from Moderna COVID vaccination.”

Wallskog disputed the determination, writing in an appeal that “an exhaustive work-up revealed no other cause of my symptoms besides my Moderna shot.”

An appeal, or request for reconsideration, sends the determination to “a qualified panel, independent of the program,” according to federal law. The panel reviews the determination and sends its recommendation back to the program, which makes the final determination.

Twenty-eight studies have documented transverse myelitis following COVID-19 vaccination, a systematic review published in October 2022 found. Those include case reports of transverse myelitis after a Moderna shot. Researchers said the exact mechanisms for vaccine-induced transverse myelitis remain unclear but posited genetic factors play a role.

Wallskog said that as of now, only people who suffer a narrow set of injuries can expect to be compensated by the U.S. government.

“Many people have this false sense that the CICP is going to be their answer, and it’s not,” he said. “All these people are going to get denied unless they have myocarditis, anaphylaxis, or certain blood clotting conditions.”

Vaccine manufacturers are not liable for injuries due to laws like the PREP Act. That leaves people with few options when they’re injured.

Wallskog helped found a group called React19, which describes itself as a “science-based non-profit offering financial, physical, and emotional support for those suffering from long-term COVID-19 vaccine adverse events.”

Drawing from a pool of donated money, the group has so far paid $556,652 to the vaccine injured, with 81 people receiving compensation.

Applicants must provide a medical note or consultation documenting symptoms and signs they’re related to vaccination.

Group officials, including Wallskog, review each application and make a determination during weekly board meetings. They give out grants of up to $10,000.

The donations come from what the group describes as a care fund.

“Unfortunately, the care fund is on hold right now because we’re low on money,” Wallskog said. “I always say we wish we had more money but at the same point we’re doing with React what our healthcare organizations and our federal agencies should be doing.”

The program could help people like Angie Bluford, who did not apply to the CICP because of the one-year deadline. Bluford wasn’t diagnosed with a vaccine injury until 18 months after getting a Moderna COVID-19 vaccination.

React19 is also advocating for reform of the CICP or moving injury claims from the CICP to the National Vaccine Injury Compensation Program, widely considered the superior option. That would require adding the COVID-19 vaccines to the routine immunization schedule, which has already been done; adding vaccines to the vaccine injury table, and congressional approval of an excise tax. Coverage under the national program should be retroactive, React19 says.

It’s taken more than a year for some injured people to get a determination. There were still 7,771 applications pending as of April 1.

One was sent in by Steve Wenger, a project manager whose COVID-19 vaccination caused Guillain-Barre syndrome, a disorder that damages the immune system.

Wenger, who got vaccinated to avoid losing his job, submitted his application in March 2022. He didn’t receive confirmation until July 2022. He’s still waiting for the outcome.

“The CICP cannot estimate when the medical review will begin or how long it may take to complete,” administrators told him in a letter.

“It’s a waiting game,” Wenger told The Epoch Times. “To be honest, I’m waiting on my rejection letter, because that’s what I’m expecting.”

Wenger’s pessimism stems from the high rejection rate and the fact no claims for Guillain-Barre syndrome have been approved despite U.S. authorities acknowledging the Johnson & Johnson COVID-19 vaccine causes the disorder.

Wenger has been dealing with large medical bills, including thousands of dollars for biweekly treatments with intravenous immunoglobulin, one of the few drugs that have helped those with lingering injuries from the vaccines. Even if CICP approves Wenger’s petition, the money likely wouldn’t last long.

“I’ve read stories that medical debt has just absolutely destroyed people, financially buried them,” Wenger said. “I never envisioned myself being one of those people. But you know, here I am.”

https://www.theepochtimes.com/in-depth-us-officials-reject-compensation-for-people-diagnosed-with-covid-19-vaccine-injuries_5216736.html

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Also see my other blogs. Main ones below:

http://edwatch.blogspot.com (EDUCATION WATCH)

http://antigreen.blogspot.com (GREENIE WATCH)

http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)

http://australian-politics.blogspot.com (AUSTRALIAN POLITICS)

http://snorphty.blogspot.com (TONGUE-TIED)

https://immigwatch.blogspot.com (IMMIGRATION WATCH)

https://awesternheart.blogspot.com (THE PSYCHOLOGIST)

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

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Has India already beaten the super-infectious new Covid variant?

India may have already beaten the Arcturus wave, according to data that destroys fears surrounding the super-infectious Covid variant.

A huge explosion in cases across the country over the past month left hospitals braced for a surge of infected patients. Some of the worst-affected states even brought back mandatory face masks out of precaution. It sparked concerns that Britain could be hit by a similar fate.

Yet India's once-spiralling curve may have petered out before it ever had a chance to overwhelm the nation. Cases now appear to be in decline, experts on the ground have claimed.

Paediatrician Dr Vipin Vashishtha, based in the north of the country, who was one of the first to raise the alarm about Arcturus when he warned it may trigger conjunctivitis in kids, said data suggests the resurgence has already 'peaked'.

Prominent Covid experts today told MailOnline the U-turn in cases was proof that concerns over XBB.1.16, as it is scientifically known, were overblown.

They also insist there's no proof the strain is any more severe than others circulating.

Professor Robert Dingwall, who advised the Government on the virus during the pandemic, also told MailOnline: 'We have to stop jumping at every new Covid variant that comes along unless there is solid evidence that we have poor immunity to it. 'We need to be treating Covid like any other influenza-like illness.'

Despite Covid cases having spiked in recent weeks, hospitals are not yet seeing huge crowds. Most patients in New Delhi — which was the epicenter during previous peaks — are elderly or battling underlying conditions.

Fearing a repeat of last year's carnage, hospitals around India conducted drills to check Covid readiness in the face of spiralling Arcturus figures.

More than 30,000 hospitals across India took part in the Covid mock drill, which involved checking availability of beds, ventilators and oxygen cylinders in the event they were overwhelmed.

In an anticipation of chaos, many provincial governments have made masks mandatory again. That includes in Mumbai, where all patients, visitors and employees at hospitals must don coverings.

Professor Francois Balloux, a vocal Covid commentator throughout the pandemic, from University College London, also told MailOnline he was 'not worried' about the variant.

'I don’t think anyone should be panicking over it, wherever they may live in the world,' he said.

'As long as we’re facing related Omicron variant lineages, replacing each other over time, we should be fine, whatever fancy name they may be given. Summer is coming. 'There’s no ugly variant raising its head and Covid should rank low among peoples’ concerns right now.

'As long as the Omicron lineage predominates - whatever variant - there will be cases, but no big nasty wave.

'If and when, the World Health Organization (WHO) decides that an emerging SARS-CoV-2 lineage should be given a new Greek letter name, things will become more serious.'

He added: 'That said, we’ll never be back to early pandemic ‘square one’, as protection against severe symptoms and deaths, provided by vaccination and prior infections will remain, long-term, whatever variant SARS-CoV-2 may throw at us in the future.'

The strain, which was first identified by the WHO in January, saw cases in India explode 90-fold within weeks.

India was logging over 10,500 Covid cases earlier this week, according to Oxford University-run platform Our World in Data.

This is up from the 160 in late February, when the variant began to gather pace. But as of April 28, this had dropped to 10,100.

Data also suggested Arcturus it made up two thirds of all cases in the country.

Dr Vipin Vashishtha, consultant paediatrician at the Mangla Hospital and Research Centre, and former official at the Indian Academy of Paediatrics, also tweeted: 'Is the peak of Indian Covid surge led by XBB.1.16 Arcturus already over? Yes the data suggests so.'

He added: 'The outbreak probably peaked around week 13/14. Therefore it's slowing down.'

India's drills and masks were a grim reminder of how the country was devastated by the Delta wave in 2021, with a total of 4.7million excess deaths, according to WHO estimates.

The nation's health system was overwhelmed by a surge of cases triggered by that Covid variant, with some hospitals even running out of oxygen.

Nowadays the illness caused by the Covid more closely resembles that of the flu, unlike during the earliest days of the pandemic.

But XBB.1.16 does have three extra mutations on its spike protein, which may help it dodge the body's natural defences.

And doctors on the front line in India have also claimed they've seen a rise in infected children with conjunctivitis, suggesting Arcturus may be causing different symptoms to other variants.

A study published on Friday also revealed the variant has been shown to increase the risk of the eye condition among children under one-year-old.

Led by Dr Vashishtha, the research found young infants were disproportionately affected than older children.

'One interesting finding was the presence of itchy, non-purulent conjunctivitis with mucoid discharge and stickiness of eyelids in 42.8 per cent of positive infants,' Dr Vipin, who also sits on the WHO's vaccine safety net, said.

The study of 25 children seen between April 4 and April 16 found the youngest case was a 13-year-old newborn baby.

But none of the children required hospitalisation.

Professor Paul Hunter, an expert in infectious diseases from the University of East Anglia, also told MailOnline today: 'Covid has previously been reported as causing conjunctivitis even back in 2020.

'Also many other respiratory viruses, especially adenoviruses, can cause conjunctivitis so not that surprising. Most cases of viral conjunctivitis are mild and recover of their own.

'The issue is excluding another cause of the conjunctivitis that has to be treated more aggressively.'

He also warned that while infections 'may have peaked in the last few days in India', it remains 'too early to be confident that this a not a temporary glitch'.

He added: 'I prefer more than just three days of falling numbers before I am content it is a trend.

'It is possible that the proportion of infections that are due to XBB.1.16 has also started falling but again it's too early for me to be confident. 'It looks like the percentage is falling but the confidence intervals are very wide.'

Scientists at the University of Tokyo comparing the Kraken and Arcturus sub-variants have suggested that the newer strain spreads about 1.17 to 1.27 times more efficiently than its relative.

They warned it 'will spread worldwide in the near future' aided by the fact that it seems 'robustly resistant' to antibodies lingering in the body from previous Covid infections.

In a briefing on April 20, the WHO confirmed XBB.1.16 'may spread globally and contribute to an increase' in cases.

The strain, while identified in January, has been monitored by the WHO since the end of March.

It has now been seen in 42 countries, including the US, Singapore, Australia, and Canada.

Other Omicron sub-variants include Kraken (XBB.1.5) and Orthrus (CH.1.1).

Currently Kraken remains dominant in the UK, causing 44 per cent of all cases, while Omicron accounts for 8 per cent.

Like similar new Covid variants, virus trackers online decided to call XBB.1.16 'Arcturus' following a pattern of naming new strains after mythological entities.

https://www.dailymail.co.uk/health/article-12007467/Has-India-beaten-super-infectious-new-Covid-variant.html

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Judge Rules Chicago Must Reinstate Employees Fired Over Vaccine Mandate, Rescind Requirement

A state administrative law judge ruled on Wednesday that Chicago must reinstate city employees who were fired for refusing to comply with Mayor Lori Lightfoot’s COVID-19 vaccine mandate and rescind the requirement.

The decision came in a case before the Illinois Labor Relations Board, involving over 20 unions representing city employees, which filed an unfair labor practices charge with the state panel after Lightfoot imposed the policy in the fall of 2021.

A separate but similar case involving the Fraternal Order of Police (FOP) Lodge 7, the city’s largest police union, remains pending.

In a 78-page decision in combined cases brought by the Coalition of Unionized Public Employees and the American Federation of State, County and Municipal Employees (AFSCME) Council 31, Administrative Law Judge Anna Hamburg-Gal found that although the city had the right to implement a vaccine requirement for its employees, it was obligated to negotiate with the union over the effects of that policy.

The judge ruled that the city should have negotiated with the unions over the consequences of the policy, such as placing non-compliant employees on “no-pay status” and later terminating their employment.

Hamburg-Gal wrote that docking pay “is not an inevitable consequence of the vaccine mandate or reporting requirement because no-pay status is not the sole means by which the (city) could have enforced its policy.”

The city also unilaterally changed the status quo in August 2021 when it began terminating employees who had not complied with the policy, choosing “to pursue a far harsher approach than it had taken before against violators of its vaccination policy.”

The judge ordered the city to reinstate the affected employees, with their personnel records expunged, and to compensate workers for any lost pay or benefits that resulted, with 7% interest.

The unions should be allowed to negotiate to keep any parts of the policy they like, the judge said.

A spokesperson for AFSCME Council 31 applauded the ruling as a “strong decision (that) will bolster workers’ rights going forward.”

Anders Lindall, AFSCME spokesman, stated, “The ruling affirms that when an employer contemplates significant changes to terms of employment, it has a duty to bargain in good faith with the union. In this case, the city did not do that.”

This deadline falls just days after Lori Lightfoot will leave office and far left Mayor-elect Brandon Johnson will take over.

While the FOP’s matter is still pending and tied up in court, the police union’s president, John Catanzara, celebrated the decision as “a great day for labor in Chicago and the state of Illinois.”

https://thefederalistpapers.org/opinion/judge-rules-chicago-must-reinstate-employees-fired-vaccine-mandate-rescind-requirement

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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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Ringing in the ears after Covid shot

Thousands of Covid vaccine recipients have reported persistent ringing in their ears after getting the shots and scientists are still investigating the connection.

The Centers for Disease Control and Prevention maintains that data does not support a link between the vaccines and the condition known as tinnitus, but the problem has become persistent and widespread enough to merit more attention.

Over 16,000 vaccine takers in the US have reported some form of tinnitus after getting the shots, while a Facebook support group called ‘Tinnitus and Hearing Loss/Impairment after COVID vaccination’ has gained 4,000 members.

The risk would be tiny even if there is a connection, given that 675million vaccine doses have been administered in the US, according to the CDC.

Dr Shaowen Bao, a neurophysiologist at the University of Arizona, Tucson’s College of Medicine and a longtime tinnitus sufferer, set out to investigate the association by sampling nearly 400 members of the Facebook tinnitus group.

While on the surface the complaints of ringing in the ears may sound like anti-vaccine propaganda, the Facebook from which Dr Bao gleaned his sample maintains that it is ‘pro-vaccine’ and does not parrot anti-vax sentiments such as claims that the shots cause deafness.

Many of the sufferers reported other symptoms, including dizziness and vertigo after their shots.

This, Dr Bao said, suggests ‘that the vaccine is interacting with pre-existing risk factors for tinnitus. If you have the risk factor, you will probably get it from the first dose.’

Tinnitus after vaccination, most often the first shot, could be caused by inflammation around the brain or spinal cord, Dr Bao said.

Dr Bao has said: ‘Vaccination is an immune response; it could cause inflammation - peripheral inflammation - and peripheral inflammation could affect the brain where the tinnitus is initiated.

Tinnitus is a common condition affecting as many as 25 percent of American adults.

Is Covid to blame for this crackling noise in my ears?

Viruses (including Covid-19) can cause tinnitus — usually as a result of inflammation which damages nerves that carry hearing information to the brain. A study last year found 20 per cent of those affected by Covid developed tinnitus.

Patients report a phantom noise in the ear that can be mild as well as extremely disruptive to daily life.

It can sound like persistent ringing, hissing, roaring, or screeching at low or high volumes.

Dr Bao found that in many cases, the tinnitus was severe, including one man who experienced such persistent ringing that he could no longer hear his radio.

The study, which has not been published, is one of just a few studies looking into the link between vaccinations and tinnitus.

A 2022 study published in the journal Laryngoscope found that the risk of developing tinnitus after the first dose of the Covid vaccine was low - and in fact, the risk was higher after receiving other vaccines such as the flu shot. But just because the risk is low does not mean it is zero.

Dr Gregory Poland, founder and director of the Mayo Clinic’s Vaccine Research Group in Rochester, Minnesota has detailed his ordeal with tinnitus after getting his Covid vaccines, telling NBC News last year that he thought the sudden noise ‘was a dog whistle going off right next to me.’

A lack of CDC-sanctioned research into the little-understood after effect of vaccination has frustrated sufferers like Dr Poland, who said the leading health agency is ‘unconcerned’ about the reports.

The true total number of people with tinnitus linked to a Covid vaccine is murky at best. In addition to the 4,000-person Facebook group, the CDC’s voluntary reporting database shows at least 16,000 entries of people who experienced tinnitus at some point after getting the shot.

Times of onset vary, with some sufferers saying the ringing came on 36 hours after vaccination while others said about a month.

Some sufferers saw tinnitus come on after their second shots, but most after their first.

The effect may also be a product of long-covid, or the lingering symptoms even after recovering from the disease. The most commonly reported among them include fatigue and brain fog, but researchers at Yale University have begun enrolling participants in a study of long covid symptoms that includes tinnitus.

Dr. Harlan Krumholz, a professor of medicine at Yale University and clinical long Covid researcher, said the tinnitus could be caused by internal vibrations in the ear.

Researchers have not pinpointed a cause for tinnitus generally, though various theories exist. A team at Stanford University’s Medicine Molecular Neurotology Laboratory suggested that forms of tinnitus reflect some damage in the inner ear.

Dr Konstantina Stankovic, an inner ear expert and head and neck surgeon at Stanford said the brain tries to compensate for the damage in the inner ear ‘and starts to make sound of its own.’

https://www.dailymail.co.uk/health/article-12008049/Covid-vaccines-tinnitus-know-far.html

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One final question for Australia's medical regualtors: Will your credibility be restored or slide further?

On 25 July 2021, Scott Morrison said the government will buy another 85 million Pfizer booster doses in 2022 and 2023. That’s more than three boosters for every Australian or more than four for every adult, after their initial two-dose vaccination. Thus the government was already aware of the vaccine’s waning effectiveness against the existing strain and its likely ineffectiveness against new variants. This of course is also the understanding about annual flu vaccines: they are reformulated every year because the pathogen is unstable and keeps mutating, which in turn rules out an eradication strategy. This is why we learnt long ago to live with the flu, focus public health efforts on protecting the most vulnerable through annual vaccines and leave the rest of society to carry on with the normal routine of life. Meanwhile, the ‘safe and effective’ messaging on Covid vaccines looks increasingly suspect. Confidence has diminished in health authorities, parliaments, medical establishments and media for their manifold failures to interrogate the official claims and report on the rising toll of vaccine injuries. As from last month, the AstraZeneca vaccine is no longer available in Australia owing to the ‘rare but serious side effect’ thrombosis. On 31 March, the ABS reported there were 25,235 (15.3 per cent) excess deaths in Australia in 2022. Yet the government and opposition MPs rejected a motion from Senator Ralph Babet to hold an inquiry into this concerning phenomenon. Meanwhile from 1 April Switzerland has withdrawn all vaccine recommendations. Doctors can administer Covid vaccines only in individual cases under specified conditions and bear the risk of liability themselves.

Even if Covid had proven to be as deadly as the Spanish flu and the vaccines 90 per cent effective, coercion and mandates would still have been unethical. Revelations that authorities knew this to be false in early 2021, means there was little medical justification either. This makes the public policy scientifically perverse and ethically immoral. Social media Big Tech made it worse by actively censoring, shadow-banning, downgrading and slapping labels from self-identifying fact-checkers better described as misinformers and disinformers. (India has gone one logical step better. The government will create a fact-check body for regulating online content. Opposition parties have denounced the move as censorship and accused the ruling party of being the biggest purveyor of fake news.) On the one hand, Big Pharma and public regulators meant to oversee them colluded to hide and delay important information. On the other, they ferociously attacked independent researchers who tried various forensic techniques to ‘mine’ the relevant data and offer a counter-narrative, with the goal of discrediting and demonising anyone with the temerity to question the official ‘truth’. The Censorship-Industrial Complex was weaponised into a powerful tool of state power in an evolving system of governance that is a threat to the very survival of free society. I am not impugning doctors and researchers who put their faith in the underlying integrity of the regulatory agencies and medical establishments, even if that faith turned out to have been misplaced and abused. I too feel betrayed by the WHO and disillusioned with its patchy performance, to put it kindly.

On 5 April Maryanne Demasi published an article on Substack, republished by Children’s Health Defense, that the triumphalist 95-per-cent-efficacy narrative of the Pfizer vaccine, which would give us all an exit ramp from the coronavirus pandemic with universal vaccination, had already gone off script by June 2021. Some highly vaccinated countries like Israel were experiencing a fresh wave of infections that was fuelling vaccine hesitancy and slowing take-up. By July Israel was reporting effectiveness of 64 per cent and in August only 39 per cent. Regulatory filings show that Pfizer and the FDA had evidence already in April 2021 on waning effectiveness. This was not publicly disclosed until much later. The press release from Pfizer on 1 April 2021 announcing results of its six-month Phase 3 trial repeated claims of 91.3 per cent efficacy against the Covid disease and up to 100 per cent effectiveness against severe disease. The top authorities continued to downplay the lack of evidence to demonstrate vaccine effectiveness against viral transmission and long-term protection. While acknowledging the possibility of breakthrough infections, Anthony Fauci said on national TV on 16 May 2021, ‘When you get vaccinated, you not only protect your own health, that of the family, but also you contribute to the community health by preventing the spread of the virus throughout the community… you become a dead end to the virus. And when there are a lot of dead ends around, the virus is not going to go anywhere’. The official report from Public Health Ontario in March shows Covid hospitalisations and deaths in 2022 were 31 and 39 per cent higher respectively than in 2021, despite 76 per cent of Ontarians being double-vaccinated.

Neither the pharmaceutical industry nor public health agencies are releasing all the data nor undertaking the important safety studies and acting on safety signals in a timely fashion to restore trust in their good faith, competence and integrity. Independent researchers are still having to do medical detective work instead. With widely varying and contested definitions and measurements of Covid and vaccine-related deaths, they look instead for clues in all-cause excess deaths. In February, Norwegian scientists published a study which found vaccination rollouts across 31 countries in 2021 were associated with rising all-cause mortality in the first nine months of 2022. A March analysis from the Vaccine Damage Project concluded there were 310,000 vaccine-related US excess deaths in 2021 to 2022 inclusive. Professor Norman Fenton calculates the number of deaths caused directly by vaccines until 23 March 2023 to be 120,000 in the US and 16,000 in the UK. Dr. Ros Jones, a retired consultant paediatrician, examined the lagged temporal correlations in several European countries between vaccine uptakes and falling births nine months later. On 28 March WHO experts published a revised roadmap which prioritises vaccines for the elderly and people with comorbidities, relegates healthy children and adolescents down to low priority because of their low disease burden and recognises natural immunity from prior infections.

In a sign they might be awakening to the risk of cross-vaccine hesitancy because of disillusionment with Covid vaccines, the guidance acknowledges: ‘The public health impact of vaccinating healthy children and adolescents is comparatively much lower than the established benefits of traditional essential vaccines for children’.

My final question is to the public health clerisy. If you become transparent on efficacy, investigate safety signals urgently and fully and publish the findings honestly, in the long run will your credibility worsen or will you begin to regain public trust and confidence?

https://www.spectator.com.au/2023/04/one-final-question-for-regualtors/

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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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Not with a bang but a lawsuit: Is this the way the Covid vaccines end?

Dr Barry Schultz was a highly respected paediatrician, surgeon and obstetrician in Adelaide. He was also a Covid vaccine skeptic. He was not opposed to conventional vaccines. He had immunised thousands of children and was fully vaccinated. He was concerned about the safety and efficacy of the Covid vaccines, so much so that when he was sent the paperwork to become eligible to administer the novel gene-based injections which were only provisionally approved he knew that if anything went wrong he was the one who could be sued. So he wrote on the back of the form ‘get stuffed’ and told his staff to send it back.

Nonetheless, he had to be vaccinated to be able to be able to treat his patients in hospitals. So on 2 October 2021 he had his first Pfizer jab. Within three days he had blood in his urine. He also suffered nose bleeds. Both are adverse events associated with Covid vaccination. He booked to see a specialist but continued to work 80 hours a week. He never got to that appointment. Two weeks after his first jab he woke at 2:30am on Tuesday 19 October haemorrhaging internally, including in his brain, and vomiting blood profusely. He was taken immediately to hospital where he was eventually pronounced dead.

It is well established in Covid medical literature that it is the spike protein – found in both vaccines and the virus – that damages blood vessels causing haemorrhaging. Given that his death occurred less than three weeks after the jab, the vaccine should be suspected of having contributed to his death. Yet his widow, a registered nurse, had to battle for over a year before the Australian Health Practitioners Regulatory Agency finally agreed to submit a report to the TGA which listed the Pfizer vaccine as being suspected of contributing to his death.

This week, his brother Phil was one of over 500 people who have joined a class action lawsuit filed in the federal court of Australia by Brisbane lawyer Natalie Strijland. All have suffered serious or life-threatening events or are the relatives of those who have died following Covid vaccination. Many have have been left with significant disabilities. As the news filters out about the class action, the first of its kind in Australia, more people are joining each day. Dr Melissa McCann, who instigated the action, is crowdfunding to assist with legal and travel costs. Any compensation awarded will be shared entirely by the injured and the bereaved.

The applicants will argue that the Therapeutic Goods Administration (TGA) did not fulfil its duty to properly regulate the vaccines which resulted in considerable harm to Australians. The respondents are the Australian government, the Department of Health and Aged Care Secretary Dr Brendan Murphy, who announced in early April that he will retire in July, and the former head of the TGA Adjunct Professor John Skerritt who just retired from the public service in mid-April.

So far there have been 986 deaths and over 138,000 adverse events that have been reported to the TGA following Covid vaccines. That dwarfs the reports of death for all flu vaccines since records began in 1971 – only 28 deaths and 3,924 adverse events. Even so, the Covid vaccine reports are almost certainly an understatement. A Harvard study commissioned by the US Department of Health and Human Services in 2010 showed that reports to the regulator of vaccine injuries may represent only one per cent of those who are injured.

Yet despite the mounting claims of deaths and injuries the TGA insists that only 14 deaths are ‘likely to be related to vaccination’ – 13 following an AstraZeneca (AZ) jab and one following Moderna.

AZ’s vaccine was quietly withdrawn from Australia on 21 March but the TGA maintains this has nothing to do with safety even though it is suspected of contributing to the deaths of 484 Australians – 100 aged 18 to 64, 342 aged 65 and above, and 42 Australians whose age is apparently unknown.

So why has the AZ vaccine been withdrawn? Could it have anything to do with the fact that the pharma giant is being sued in the UK by a group representing the vaccine injured and dead which includes the husband of popular BBC North radio broadcaster Lisa Shaw? She was only 44 when she died a week after her AZ jab of vaccine-induced immune thrombotic thrombocytopenia, an acknowledged sometimes deadly side effect.

What about Pfizer? It seems highly unlikely that not a single death has been caused by its vaccines in Australia when smaller countries such as New Zealand and Singapore acknowledge that it has caused deaths. There have been over 5,300 reports of myocarditis and/or pericarditis in people following Covid vaccination, both of which can be caused by Covid vaccines. In 23 cases the person died and in 16 of those cases it was following a Pfizer vaccine. These were not elderly people. In seven cases the person was aged between 18 and 64, in six cases they were aged 65 and above and in three cases the age was unknown.

How is it possible not to know someone’s age when they die when the TGA claims it is ‘carefully monitoring and reviewing reports of myocarditis and pericarditis’ and ‘closely reviews all deaths reported in the days and weeks after Covid-19 vaccination’? These facts should be easy to establish. The name, age and type of vaccine administered are recorded on the Australian Immunisation Register for every vaccination in Australia and the age of death is recorded on every death certificate. Yet in 28 deaths the TGA has not identified the type of vaccine and in 92 deaths the TGA says that it doesn’t know the age of the person.

What is surprising is not that the TGA has withdrawn the AZ vaccine but that it is still recommending all other Covid vaccines to anyone aged 5 years or older. Denmark, Sweden and Norway stopped recommending the vaccine for children and healthy adults at different points in 2022. Even the World Health Organisation urged countries this April to treat vaccinating healthy children and adolescents as a ‘low priority’. Switzerland, the global headquarters for many pharmaceutical companies, has said that at present it no longer recommends Covid vaccinations for anyone. Doctors may still administer the jabs but will bear the risk of liability. Is this the way the Covid vaccines will end, not with a bang but a lawsuit?

https://www.spectator.com.au/2023/04/not-with-a-bang-but-a-lawsuit/

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More on the Class action lawsuit over Covid vaccine injuries 'There has been a cover-up'

A landmark Covid-19 vaccine injury class action lawsuit has been filed against the Australian government and the medicines regulator.

The nation-wide suit, which reportedly has 500 members including three named applicants, seeks redress for those allegedly left injured or bereaved by the Covid-19 vaccines.

One of the applicants who suffered a severe heart condition after getting the Pfizer jab is even claiming there was 'cover-up' during the vaccine rollout which hid the potential risks.

The federal government, the Therapeutic Goods Administration (TGA) and the Department of Health - in addition to a number of senior public servants - are all named as parties to the class action, which was filed in the New South Wales Federal Court on Wednesday.

The named parties are accused of negligence in their approval and monitoring of Covid-19 vaccines, breach of statutory duty and misfeasance in public office.

The lawsuit was organised by Queensland GP Dr Melissa McCann who raised over $105,000 through crowd funding. 'These injured and bereaved have suffered immense loss, pain and grief,' Dr McCann tweeted.

'Just as heartbreaking has been the gaslighting and silence, which has left them feeling abandoned. We cannot simply 'move on' from covid and leave them behind.'

Dr McCann has been critical of the existing compensation scheme, claiming it was 'not fit for purpose'.

'Many vaccine-injured Australians who cannot access compensation through the Services Australia scheme now find themselves abandoned, with no support,' Dr McCann said.

The size of the compensation claim being sought is not yet clear.

The TGA has been contacted for comment.

The TGA’s latest health safety report, published on 20 April, reveals that adverse risks are extremely low. here were 138,307 total adverse event reports from nearly 66 million vaccine doses administered - a rate of just 0.2 per cent.

'The protective benefits of vaccination far outweigh the potential risks,' the report states.

The medicines regulator has identified a total of 14 reports where the cause of death was linked to vaccination and said there was no new vaccine-related deaths identified since 2022.

'The TGA closely monitors reports of suspected side effects (also known as adverse events) to the COVID-19 vaccines,' it said.

'This is the most intensive safety monitoring ever conducted of any vaccines in Australia.'

But instructing solicitor Natalie Strijland, of Brisbane law firm NR Barbi, said the action would argue the TGA caused considerable harm and damage by failing to regulate the COVID-19 vaccinations properly.

The class action names three applicants, one of whom is 41-year old father-of-two Gareth O'Gradie.

Mr O'Gradie, a teacher from Melbourne, was left with a 20-centimetre scar down his chest after developing severe pericarditis — inflammation of the lining around the heart — following his first Pfizer vaccination in July 2021.

He did not respond to various medications and therapies and in February 2022 doctors performed open heart surgery to remove his the pericardial sac lining his heart.

The TGA said myocarditis and pericarditis were 'usually temporary conditions, with most people getting better within a few days', noting that the Australian Technical Advisory Group on Immunisation (ATAGI) 'continues to emphasise that the protective benefits of the vaccines far outweigh the rare risk of these side effects'.

But Mr O'Gradie believes there has been 'misinformation about the safety' of the vaccines from the government. 'I think there has been some cover-up,' he told news.com.au.

'There was a lot of, you know, 'We need to not scare the public as part of the vaccine rollout, so let's not publicise these things.' There was a large, intentional withholding of information — that doesn't give people informed consent.'

He claimed that he was 'totally not or never have been anti-vaccine'. 'I'm pro-science, I'm well educated,' he said.

Mr O'Gradie told The Australian that he was worried about the 'anti-vaccine lobby piggybacking' on the class action.

He is joined by two other lead claimants: Antonio Derose, 66, who developed encephalomyelitis (inflammation in the brain and spinal cord) following his AstraZeneca jab and Anthony Rose, 47, who claims severe cognitive impairment and chronic fatigue following his Moderna vaccination.

The existing compensation scheme, which is open to Australians who 'suffer a moderate to severe impact following an adverse reaction to a TGA-approved COVID-19 vaccine', has been heavily criticised for being difficult to access and too narrowly focused.

As of April 12, Services Australia had received 3501 applications and paid 137 claims totalling more than $7.3 million. Another 2263 claims are still in progress, while 405 have been withdrawn and 696 deemed not payable.

https://www.dailymail.co.uk/news/article-12015497/Australian-government-hit-class-action-lawsuit-Covid-vaccines.html

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Also see my other blogs. Main ones below:

http://edwatch.blogspot.com (EDUCATION WATCH)

http://antigreen.blogspot.com (GREENIE WATCH)

http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)

http://australian-politics.blogspot.com (AUSTRALIAN POLITICS)

http://snorphty.blogspot.com (TONGUE-TIED)

https://immigwatch.blogspot.com (IMMIGRATION WATCH)

https://awesternheart.blogspot.com (THE PSYCHOLOGIST)

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

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Very weak study in defence of masks

The journal Plos One on Friday slapped an “expression of concern” on the Burnet Institute’s controversial July 2021 paper, which purported to show that mandating masks was the “single most important control measure” that turned around Victoria’s second Covid wave in 2020 “almost overnight”.

In October 2021, experts told news.com.au that the supposed “world-first” study was riddled with basic errors and should never have been published in a major journal, blasting the paper as “crap”, “extremely lightweight” and “very, very low quality”.

The Burnet Institute – an influential public health body that advised the Victorian government on its Covid response – stood by its findings and described the scientists’ comments to news.com.au as “disappointing and unprofessional”.

But Plos One has now acknowledged flaws in the study with a lengthy notice appended to the paper. An expression of concern – one step above a correction but short of a retraction – is used to “alert readers of serious concerns about published work”.

“After publication of this article, readers raised a number of concerns, including about the methodology, the limitations of the study design, and whether the conclusions are fully supported,” Plos One editors wrote in the notice.

“The Plos One editors consulted with two members of the editorial board and a statistical advisor who advised that the study design is associated with a number of weaknesses that are discussed in the article, and which are unavoidable because of ethical issues that would be associated with a randomised controlled trial in the context of a pandemic, but that there were also additional weaknesses.”

For the study, the Burnet Institute looked at photos from The Age newspaper to conclude that mask usage rose from 43 per cent to 97 per cent after the July mandate came into effect.

Medical researcher Dr Kyle Sheldrick told news.com.au in 2021 that it was “hard to think of a worse methodology to answer this question than just looking at which photos are collected by a metropolitan newspaper”.

“I was staggered to see this was published by a major journal,” he said. “If a student came to me and said, I’m going to compare these two sets of photos and draw some conclusion about whether a policy worked, you would send them away to think about it.”

Another researcher, an eminent Australian clinician and scientist who spoke on the condition of anonymity, was equally scathing. “I agree, it’s crap,” he said. “It’s extremely lightweight. I think it’s a totally feeble article. It doesn’t have a rigorous methodology and it is weak in its scientific inference.”

Concerns were also raised about other aspects of the paper, including that it singled out the mask mandate as the key reason for the fall in Covid transmission out of all of Victoria’s sweeping lockdown measures.

Plos One’s editors acknowledged the three main issues raised with the paper – the photographic observation of mask usage, self-reported mask wearing survey data, and unmeasured confounding variables such as curfews, movement restrictions and closures.

On the photos, Plos One’s editors noted it was “unclear whether such images are representative of mask usage in the population”.

They also noted the Survey of Covid-19 Responses to Understand Behaviour (SCRUB) sample size was “small and may not be representative of the population”.

In response, the Burnet Institute’s authors indicated that “the sample sizes were not inappropriately small for the purpose, noting that the high-powered interrupted time series study found a highly statistically significant change in the growth rate of the epidemic that coincided with the mask mandate”.

Plos One’s editors also noted that “the study design could not exclude the possibility of contributions from unmeasured confounding variables, including the implementation of a curfew and movement restrictions on 2nd August 2020 and closure of childcare facilities, schools, and non-essential businesses on 5th August 2020”.

“According to the cumulative expert input received by the Plos One editors, the results of the published study contribute to the field of mask evaluation research, provided results are not overinterpreted and limitations are acknowledged,” they wrote.

“The Plos One editors felt that the conclusions, including those that imply causation, a direct correlation between Covid-19 cases and mask mandates, and the ability of masks for controlling epidemics, were not suitably tempered in light of the limitations of the study design. The Plos One editors issue this expression of concern to inform readers about the above considerations regarding study design and interpretation of the results.”

The Burnet Institute has been contacted for comment.

It comes after a major Cochrane Review – considered the gold standard of evidence-based medicine – earlier this year assessed 78 high-quality scientific studies, and found “wearing masks in the community probably makes little or no difference” when comparing masking with non-masking to prevent Covid.

The bombshell findings proved controversial and sparked a war of words between Karla Soares-Weiser, editor-in-chief of the Cochrane Library, and the study’s lead author Tom Jefferson.

“Many commentators have claimed that a recently-updated Cochrane Review shows that ‘masks don’t work’, which is an inaccurate and misleading interpretation,” Soares-Weiser said in a statement in March.

“[The study’s] wording was open to misinterpretation, for which we apologise. While scientific evidence is never immune to misinterpretation, we take responsibility for not making the wording clearer from the outset.”

Jefferson subsequently hit back at suggestions the apology from Soares-Weiser meant the study had been retracted.

“It was upsetting,” he told journalist Maryanne Demasi. “Cochrane has thrown its own researchers under the bus again. The apology issued by Cochrane is from Soares-Weiser, not from the authors of the review.”

Jefferson claimed Soares-Weiser, in response to media pressure, had “gone outside the normal channels and made decisions without any consultation with the authors of the review”.

“It is unacceptable,” he said. “We are the copyright holders of the review, so we decide what goes in or out of the review. We do not change our reviews on the basis of what the media wants.”

https://www.news.com.au/technology/science/human-body/burnet-institute-mask-study-hit-with-expression-of-concern-notice-by-journal-plos-one/news-story/fb467b8bb49c852803c490f6c1e69152

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Face masks may raise risk of stillbirths, testicular dysfunction and cognitive decline due to build-up of carbon dioxide, study warns

Face masks may raise the risk of stillbirths, testicular dysfunction and cognitive decline in children, 'explosive' new research suggests.

A review of dozens of studies on face coverings suggested they can cause mild carbon dioxide poisoning when worn over long periods.

The German academics who carried out the research believe masks create a pocket of dead space between the mouth and mask, which traps the toxic gas.

They say the build-up of CO2 in pregnant women's bodies could cause complications for the unborn fetus. They point out that CO2 also contributes to oxidative stress, which can affect cognition and cause testicular issues in men.

But independent doctors have questioned the conclusions of the study — which never directly looked at health complications and mask use, describing the link as 'unlikely'.

Alluding to the surge in stillbirths during the pandemic, the German researchers said: 'Circumstantial evidence exists that popular mask use may be related to current observations of a significant rise of 28 percent to 33 percent in stillbirths worldwide.'

'[And] reduced verbal, motor, and overall cognitive performance of two full standard deviations in scores in children born during the pandemic,' the researchers wrote in the paper, published in the journal Heliyon.

But the study could not conclusively prove that the masks were directly responsible for any of these complications.

Dr Stuart Fischer, an emergency care physician in New York, questioned whether there was a 'toxic buildup' of CO2.

He said: 'I wouldn’t say this happens, because the body adjusts the pH, the acid/base balance very quickly. Respiratory acidosis due to facemasks is unlikely although short-term side effects might affect people with chronic lung disease.'

The German research team gathered data from 43 previously published studies on exposure to CO2, mask-wearing and pregnancy.

They found that after wearing a mask for more than five minutes, CO2 levels in the inhaled air rose to between 1.4 percent and 3.2 percent.

One mask study conducted in Germany, researchers measured the CO2 concentration of air behind surgical masks worn by 15 healthy men. Within 30 minutes, the CO2 concentration rose to roughly 2.8-3.2 percent.

In another study in Italy, scientists measured the air under surgical masks worn in a lab and found a concentration between 0.22 and 0.29 percent within five minutes.

Masks provide breathing resistance and create a dead space that traps CO2, leading to more inhaled and re-breathed CO2, the reviewers said.

The gas makes up around 0.04 percent of all inhaled air, for comparison, and the Department of Agriculture said safe levels should be below 0.5 percent for eight-hour exposure.

The researchers then looked at studies that focused on the effect of similar CO2 levels on animals such as mice and rats.

Mammals such as mice and rats with prolonged exposed to 0.3 percent carbon dioxide gave birth to offspring which had 'irreversible neuron damage', the review found.

In total, the researchers looked at studies dating back from the start of the scientific databases they searched until November 30, 2021.

The main caveat of the research is that the studies looking at the potential toxic effects of carbon dioxide are animal studies - because these experiments would not be ethical in humans.

The researchers also noted that none of the studies in their review looked directly at mask use and miscarriages, infertility and neurodevelopment disorders.

The researchers also noted that the exact effects of toxic levels of CO2 on unborn life is not known in great detail.

Carbon dioxide is known to contribute to oxidative stress, which the researchers suggested would hinder fetal development.

Dr Kevin Bass, cell and molecular biology PhD student, said on Twitter that the new paper was 'explosive'.

But he said: 'We do not have any good evidence in pregnant women... of the long-term effects of mask-wearing and therefore no evidence that these effects occur in women.'

He added: 'All we have are animal studies and a clear indication that changes in CO2 concentrations do occur in mask-wearing women.'

Stillbirths and pregnancy complications rose during the Covid pandemic, and preeclampsia and other pregnancy complications were blamed on the virus.

Factors other than mask-wearing are likely to be at play, such as hospital closures and delayed care.

It comes after three years of fierce debate about the effectiveness of masks.

Mask mandates on transportation systems in America were backed by penalties of up to $3,000 for repeat offenders.

Former director of the National Institute of Allergy and Infectious Diseases Dr Anthony Fauci initially advised people not to wear masks, which he later claimed because he was concerned there would not be enough for healthcare workers.

He went on to advise that everyone should wear a mask.

https://www.dailymail.co.uk/health/article-11982039/Face-masks-raise-risk-stillbirths-testicular-issues-cognitive-decline-study-says.html

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Also see my other blogs. Main ones below:

http://edwatch.blogspot.com (EDUCATION WATCH)

http://antigreen.blogspot.com (GREENIE WATCH)

http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)

http://australian-politics.blogspot.com (AUSTRALIAN POLITICS)

http://snorphty.blogspot.com (TONGUE-TIED)

https://immigwatch.blogspot.com (IMMIGRATION WATCH)

https://awesternheart.blogspot.com (THE PSYCHOLOGIST)

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

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Dentists: Unexplained Pain, Tooth Loss and Bone Problems May Be Linked to COVID-19 Vaccine

Before business owner and busy mom Alana Parker experienced severe oral pain and facial swelling after receiving Pfizer’s COVID-19 vaccine in 2021, she had good dental health with never so much as a cavity.

When her symptoms progressed and an ulcer had grown to the point where the bone was protruding, causing her to lose large fragments of her jawbone, Parker knew she was in serious trouble.

“I was begging them to pull my tooth out but there were no signs of it being decayed,” Parker told The Epoch Times, noting she was passed back and forth between a dentist and endodontist trying to determine what was wrong.

It wasn’t until Parker found Alabama orofacial pain and dental sleep medicine specialist Dr. Amy Hartsfield that she felt she was on the road to recovery.

Hartsfield, a private practice dentist in Homewood, Alabama, obtained her specialization from the American Board of Orofacial Pain and the American Board of Dental Sleep Medicine after practicing 14 years of general dentistry.

Parker isn’t the only patient she’s seen with severe facial pain issues. Since the vaccines were rolled out, Hartsfield has seen an exponential increase in patients with head and facial neurovascular and myofascial pain, including headaches, toothaches not caused by the tooth, osteonecrosis of the jaw, sleep issues, tinnitus, and oral and facial autoimmune conditions.

“I’ve seen patients with no previous history of health issues [who] have perfectly healthy teeth and now have pain syndromes associated with these healthy teeth,” she said. These types of injuries affect both the nerves and blood vessels.

Dental Issues and COVID-19

In her research, Hartsfield discovered an array of health issues the COVID-19 vaccine spike protein can cause, many of which are related to immunity and blood microclots.

She also discovered that this is the first time polyethylene glycol (PEG) has been used in a vaccine. The use of PEG has become increasingly controversial since it can cause a number of serious immunological reactions, including anaphylaxis, which can be life-threatening.

The vaccine has been shown to cross the blood-brain barrier, circulate throughout the bloodstream, and has been found in most organs, all with the potential for serious health consequences.

Since the blood supply is important to all areas of the body including the bones, microclots can have a detrimental effect on bone health.

Microclots and Orofacial Bone Loss

There are tiny capillaries that feed the bone, and with microclots occurring in the orofacial area, you’re going to start losing bone density around it, Hartsfield explained.

Cheryl Alverson, 79, came to Hartsfield after having all of her lower teeth extracted due to a massive recurring infection that caused extensive bone loss.

Hartsfield immediately ordered multiple blood tests, including several specifically related to blood clotting. “They showed I had microclots all through my body,” said Alverson.

Hartsfield explained that microclots can interfere with bone healing after extractions. What happened with Alverson typically only occurs in patients who have been on osteoporosis medication or had radiation therapy, neither of which applied to Alverson.

Alverson had received the Moderna COVID-19 vaccines and a subsequent booster shot before her issues began, and she had not been infected with the COVID-19 virus prior to seeing Hartsfield.

She had good teeth but spontaneously had pain in her lower left jaw. Shards—pieces of her mandible—broke off out of her gum tissue, she said.

Parker’s case started only a few months after she had received the COVID-19 vaccine. With Parker, there was a “dying off of the bone,” said Hartsfield.

Parker’s bloodwork showed extreme inflammation across multiple body systems—and with four loose teeth and not enough energy to drive a car, Hartsfield built a team around her of five specialists and put her on a protocol of medications and vitamins to support her recovery. (pdf)

Microclots not only interfere with bone health but can affect the nerves, which also rely on capillaries for survival. Without adequate blood supply to the nerves, they too will develop problems, said Hartsfield.

A Surge in Facial Pain

Birmingham, Alabama-based endodontist Dr. John Collier told The Epoch Times he’s seen an “unbelievable amount of increasing facial pain” in the last couple of years.

He refers his patients to Hartsfield if he determines the pain is not caused by the patient’s tooth.

I had a patient with tremendous facial pain, implants, and an implant allergy, said Collier. Hartsfield is the “detective who goes through all the layers of what’s causing this,” he said.

While Collier can’t say whether or not his patients’ conditions were caused by the COVID-19 vaccine, he’s confident that stress from the pandemic and the country’s toxic political environment are contributing factors.

“There’s a lot of clenching and grinding and a lot of muscular pain,” he said.

Likewise, oral surgeon Dr. Doug Denson from Birmingham, Alabama, who has also sent patients with facial pain to Hartsfield, said it’s impossible to say for sure whether it’s COVID or the vaccine causing the symptoms he’s been seeing.

“In my opinion, correlation does not always equal causation … again, there have been some odd symptoms since the pandemic started. It’s just impossible to tell the exact mechanism or cause,” he said.

Still, Denson noted the uptick of unexplainable pain symptoms in a significant portion of the population affected by COVID immediately after the pandemic started, specifically trigeminal neuralgia, which is sudden, severe facial pain.

Hartsfield has also seen an increase in neuropathy of the trigeminal nerve, as well as major issues related to inflammation and cytokine storms.

Increase in Inflammation and Cytokine Storms

Cytokines themselves are small proteins released by cells in the body, including those of the immune system where they coordinate the body’s response to fight infections and trigger inflammation.

Hartsfield isn’t the only practitioner who has noted an escalation in inflammatory abnormalities and cytokine storms since the onset of COVID-19 and the COVID-19 vaccines.

Denson has also seen an increased number of patients of all different ages with inflammation of the tongue and hyper-inflammatory responses, including osteomyelitis, an infection of the jaw that is very difficult to treat because the blood supply to the jaw is not great.

These maladies would typically be seen in older individuals rather than in a younger, healthy population.

Dr. Liz Kivus, a periodontist practicing in Alabama, told The Epoch Times she has also seen a marked increase in inflammatory symptoms such as gingival inflammation, since COVID-19 and the related vaccines.

Kivus further noted an increase in lichen planus, an inflammatory condition of the skin and mucous membranes that often results in an itchy rash that can affect various areas of the body, including the mouth, arms, legs, trunk, nails, and scalp.

We see this when patients’ immune systems are broken down, said Kivus. Patients have even said, “I’m too uncomfortable to brush my teeth and to eat.”

After seeing so many patients with unexplained issues since the pandemic and when COVID vaccines were released, Hartsfield believes it’s important to consider a patient’s vaccination status.

Consideration of Vaccination Status

“I have to screen these people to see if they’ve been vaccinated, when and how many times, and then I see if I can treat them,” said Hartsfield.

Most practitioners are not asking when the patient had COVID or when the patient had their vaccines, she said.

Hartsfield attributed some of her knowledge as coming from highly publicized critical care doctors who were “canceled” during the pandemic, including the Front Line COVID-19 Critical Care Alliance.

She also studied the information released by Department of Defense whistleblower Lt. Col. Theresa Long, M.D., MPH, an aerospace medicine doctor and Army Brigade flight surgeon who reported the unusual diagnoses and alarming trends after the introduction of COVID-19 vaccinations.

“When you ask the whole population to have a mandatory vaccine that has more side effects than any other vaccines in history showing in the Vaccine Adverse Event Reporting System from Centers for Disease Control and Prevention data, you will definitely see injuries,” said Hartsfield.

She noted that some patients and practitioners do not consider whether the patient’s ailments may have resulted from the COVID vaccine, while others come into her office knowing that their health issues directly relate to taking the vaccine.

It is really sad, she said. I just had a 25-year-old man in my office stating he has been gaslit by a number of practitioners when he mentioned his head and ear pressure had started within days of taking the vaccine, said Hartsfield. He was reluctant to tell me he thought his health issues were from the vaccines because other providers made him feel crazy.

Parker, who to this day still has elevated C-reactive protein and some orofacial pain and swelling, attributed her symptoms to a short-circuiting of the immune system and microclots.

“I’ve been chronically ill for nearly a year and unfortunately my two 12-year-old girls have seen me sick over and over—I think that has been alarming for them,” said Parker. “It’s been a journey—I don’t feel that it’s going to kill me but it was touch and go there for a while.”

“I hate that we haven’t been able to openly talk about it because I had the resources and freedom to receive treatment,” said Parker. “I can’t imagine people that do not have the resources to treat it.”

https://www.theepochtimes.com/health/dentists-unexplained-pain-tooth-loss-and-bone-problems-may-be-linked-to-covid-19-vaccine_5201385.html

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RFK Jr. Says Middle Class Was ‘Systematically’ Wiped Out by COVID-19 Lockdowns

Democratic 2024 presidential candidate Robert F. Kennedy Jr. said COVID-19 lockdowns across the United States decimated the middle class, suggesting that it has yet to recover.

“The strength of a nation comes from a strong economy and a vibrant middle class,” Kennedy told Fox News over the weekend, “and we have wiped out the middle class in the country systematically.”

The 69-year-old, who is a prominent skeptic of vaccines, stated that COVID-19-related policies benefited the elite ruling class at the cost of the middle class. Those lockdowns, he asserted, shifted $4 trillion in wealth from the middle class to a “new aristocracy of billionaires.”

Those lockdowns “created 500 new billionaires,” Kennedy stated. “The Oxfam report, which came out this week, shows that the billionaires that existed at the beginning of the pandemic, the people like Bill Gates, Mark Zuckerberg, Jeffrey Bezos, Bloomberg, etc., increased their wealth by 30 percent during the pandemic. From the lockdowns. And [Bezos’s] Amazon got to shut down all of its competitors.”

And Kennedy, the son of former Sen. Robert F. Kennedy and nephew of former President John F. Kennedy, stated that he believes that former President Donald Trump initiated those lockdowns.

Kennedy added, “I’m in a better position to run against Donald Trump than any of the Democrats because I can hold him accountable for the worst thing that he did, which was the lockdowns.”

However, Trump, as president, had little authority to issue lockdowns at the state or local level. And in early 2020, Trump said that keeping the United States shut down would “ultimately inflict more harm than it would prevent.” For those remarks and others, mainstream media outlets frequently criticized Trump and essentially blamed his policies for the rise of COVID-19-related deaths that year.

“It’s important for all Americans to recognize that a permanent lockdown is not a viable path forward producing the result that you want or certainly not a viable path forward,” the president said in April 2020, about two months after the first COVID-19 cases were detected inside the United States after spreading from mainland China.

https://www.theepochtimes.com/rfk-jr-says-middle-class-was-systematically-wiped-out-by-covid-19-lockdowns_5215413.html

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Also see my other blogs. Main ones below:

http://edwatch.blogspot.com (EDUCATION WATCH)

http://antigreen.blogspot.com (GREENIE WATCH)

http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)

http://australian-politics.blogspot.com (AUSTRALIAN POLITICS)

http://snorphty.blogspot.com (TONGUE-TIED)

https://immigwatch.blogspot.com (IMMIGRATION WATCH)

https://awesternheart.blogspot.com (THE PSYCHOLOGIST)

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

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