Public Skepticism Grows in China as Officials Downplay COVID-19 Amid "Pneumonia" Outbreak

Public skepticism is growing in parts of China as health authorities attribute an ongoing pneumonia outbreak to influenza while downplaying COVID-19 infections.

Interviews with The Epoch Times with local Chinese found that the official rhetoric regarding the outbreak has been unconvincing, with many suspecting the infections are another round of COVID-19.

Residents in major cities such as Shanghai and Tianjin have reported severe infections in their communities, including “white lung” symptoms, which are typical in severe COVID-19 cases.

China’s National Health Commission spokesperson, Mi Feng, said on Jan. 14 that the current respiratory diseases are still mainly influenza, adding that the COVID-19 infection rate is low.

On Jan. 18, China’s National Influenza Center released its latest weekly influenza surveillance report, which found that the number of emergency department visits for respiratory infectious diseases in major hospitals has increased.

The main pathogen is the influenza virus, which will still be in the epidemic period over the next few weeks, according to the report.

However, as pointed out by medical experts, COVID-19 has never disappeared in China. In recent months, pneumonia infection cases soared across the country, exhibiting similar symptoms as COVID-19, with hospitals constantly overcrowded.

Chen Yun (pseudonym), a medical worker in the mega port city of Tianjin in north China, told The Epoch Times: “The government does not report, test, or manage the current epidemic, and does not take the epidemic as a priority at all.”

She said that currently, more people are suffering from white lung symptoms.

Mr. Zhang, also a Tianjin resident, told The Epoch Times that many people have been infected in this wave of the epidemic, many of whom are seriously ill and have developed white lungs.

“There must be some deaths from it, but the government just doesn’t report them,“ Mr. Zhang said. ”There are currently no beds available in hospitals; people have to wait in line for at least a day to get admitted.”

He said that both his parents were infected and were hospitalized a few days ago.

“It should be pneumonia; the chest X-ray looks pretty serious,” he said.

“After the doctor saw the chest X-ray, he said that the patient’s lung infection was quite serious, but the doctor didn’t say what virus he was infected with. In fact, they knew it but just didn’t say it,” he said.

“The doctor just said that they should be hospitalized for IV (intravenous ) treatment as soon as possible. There is no effective treatment in the hospital, and they are just putting them on IV treatment.”

Mr. Zhang said that the official media is simply not reporting on the mass infections as they should.

Mr. Chen, a Shanghai citizen, told The Epoch Times that it is now the fourth year of the COVID-19 pandemic.

He said some people around him are currently infected, and their symptoms are quite severe.

A female colleague of his, who is about 35 years old and is the mother of two children, had an infection, and half of each lung became white.

“She requested to have a chest X-ray, and the X-ray revealed the white lungs. If she hadn’t requested, the hospital wouldn’t have taken a chest X-ray for her,” Mr. Chen said.

“As for the official data, I feel there are many problems. Sometimes they say it’s influenza A, and sometimes they say it’s influenza B. I think they must be covering something up.”

Mr. Chen complained about reporting on the issue in the state-run media, adding that reports on COVID-19 infections have been mentioned but given little attention.

Mr. Chen believed the intention of such official reporting is “in the future (when the epidemic gets very serious) it will say: ‘We reported it at the beginning’. But when they made the announcement, they couldn’t say it directly and tried to downplay it. The government needs pretty data in many aspects to make it look good, so it has to fake it, and it has ways to fake the data.”

https://www.theepochtimes.com/article/public-skepticism-grows-in-china-as-officials-downplay-covid-19-amid-pneumonia-outbreak-5573535?ea_src=au-frontpage&ea_med=world-left-0

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Could Serum Protein Changes Link to Long COVID?

Could serum protein changes be the culprit behind long COVID? Could this observation done via a study of blood samples lead to possible biomarker for a long COVID diagnosis and maybe even treatments? Carlo Cervia-Hasler with University Hospital Zurich, University of Zurich and colleagues from multiple academic medical centers report the findings of a longitudinal analysis of blood serum from 113 patients who either fully recovered from COVID-19 or developed Long Covid, as well as healthy controls. Using high-throughput proteomics approaches, Cervia-Hasler et al. measured serum levels of 6596 human proteins across study participants. Those with confirmed acute COVID-19 were followed for up to a year, and their blood serum was sampled again at 6 months and at 12 months where possible. Patients experiencing Long Covid exhibited changes to blood serum proteins, indicating dysregulated activation of the complement system, altered coagulation, and tissue injury, suggesting ongoing thromboinflammatory responses.

The Problem

Approximately 20% of patients diagnosed with COVID-19 and about 5% of all SARS-CoV-2–infected persons develop lingering symptoms, called Long Covid, that can persist for many months. Symptoms of Long Covid can include fatigue, post-exertional malaise, and cognitive impairment, and involve multiple organs. Although previous studies have shown that patients with Long Covid display signs of immune dysfunction, persistent immune cell activation, and autoimmune antibody production, the root cause of Long Covid is poorly understood, and diagnostic biomarkers for the condition aren’t well defined. Currently, Long Covid also lacks an effective treatment.

Study Findings

In this latest study published in the November 2022 study in Science Translational Medicine investigators identified persistent neutrophil-associated immune signatures in pulmonary Long Covid.

The study’s authors demonstrate that at the cellular level, the thromboinflammatory signature associated with Long Covid was linked with increased monocyte-platelet aggregates.

Dysregulation of complement proteins may contribute to the thromboinflammation associated with Long COVID. The findings of the study identify potential biomarkers for Long Covid and new treatment strategies that warrant further diagnostic and therapeutic investigation. “Although therapeutic interventions with coagulation and complement inhibitors in acute COVID-19 produced mixed results, the pathological features specific for Long Covid suggest potential interventions for clinical testing,” writes Wolfram Ruf in a related Perspective.

https://www.trialsitenews.com/a/could-serum-protein-changes-link-to-long-covid-c0fa567f

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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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COVID Vaccines Could Trigger Vasculitis, Damaging Multiple Organs

Various diseases associated with COVID-19 vaccines have been reported. A recent case study indicated that COVID-19 vaccination may trigger the development of anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitis, potentially damaging multiple organs. Among 29 patients, five underwent plasmapheresis treatment (the separation and replacement of plasma from blood), and five relied on dialysis therapy.

ANCA-associated vasculitis can cause damage to small blood vessels. Since these are distributed throughout the body, any part of the body can be affected, with the most common areas being the lungs, kidneys, joints, ears, nose, and nerves.
Neutrophils are a type of white blood cell that aids the body in fighting infection and healing injuries. ANCA are harmful autoantibodies that bind to neutrophils in the blood, releasing toxic substances and damaging the walls of small blood vessels. This can also result in the migration of neutrophils through blood vessel walls, inducing inflammation in the surrounding tissues. Additionally, it releases signaling factors that attract even more neutrophils, perpetuating inflammation and further damaging small blood vessels.

Case Report of ANCA-Associated Vasculitis

A case report published in Case Reports in Nephrology in April 2023 detailed an 82-year-old woman with high blood pressure who, after receiving her third booster COVID-19 vaccine booster, developed myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA)-associated vasculitis. MPO-ANCA is one of the primary autoantibodies in ANCA-associated vasculitis.

The patient received two doses of the Pfizer vaccine in May and June 2021, followed by a Moderna booster shot in early February 2022. The next day after the booster shot, she experienced a headache, which subsided after three days. However, starting in early March, her body temperature began to rise, accompanied by general malaise.

Upon examination, no apparent bacterial infection was found, but blood tests revealed an inflammatory reaction. The C-reactive protein level was elevated, and her white blood cell count was 13,000/microliters (the normal range is between 4,000 and 10,000/microliters), suggesting a bacterial infection. The doctor prescribed antibiotics for seven consecutive days, but there was no improvement.

The patient was later admitted to the hospital. Physical examination and imaging tests did not reveal fever, and kidney size and structure appeared normal. However, microscopic analysis uncovered hematuria (blood in the urine) and urinary protein. Additionally, the MPO-ANCA level was notably high. A kidney biopsy revealed cellular crescents in six glomeruli—the tiny filters inside the kidneys—and mild inflammation.

Furthermore, immunofluorescence confirmed pauci-immune glomerulonephritis. This is a rare small vessel vasculitis associated with rapidly progressive glomeruli inflammation, clinically characterized by kidney issues such as urinary abnormalities (hematuria and proteinuria) and high blood pressure resulting in kidney failure within days or weeks. Based on the pathological findings, the patient was diagnosed with renal-limited MPO-ANCA-associated vasculitis.

The patient was put on a steroid medication, and symptoms such as fever, malaise, and inflammatory reaction improved, while both hematuria and urinary protein disappeared. The doctor gradually reduced the steroid dosage, cutting it in half, and the patient’s condition stabilized.

The researchers stated that blood and urine tests conducted on the patient before her third vaccine dose did not reveal kidney damage or abnormalities, suggesting an association between the COVID-19 vaccine and the onset of MPO-ANCA-associated vasculitis.

The researchers suggested that the possibility of MPO-ANCA-associated vasculitis should be considered for patients experiencing fever, prolonged general malaise, hematuria, or kidney impairment after receiving a COVID-19 mRNA vaccine, especially Moderna, as was the case with this patient.

5 COVID-19 Vaccines Related to ANCA-Associated Vasculitis
An increasing number of reports indicate that widespread vaccination has led to the development of vasculitis in some people, resulting in damage to multiple organs.

A case-based review reported five types of COVID-19 vaccines linked to ANCA-associated vasculitis.

The study included cases from 29 patients, with 22 receiving mRNA vaccines (Moderna and Pfizer), four receiving AstraZeneca, two receiving Covaxin, and one receiving Johnson & Johnson. They all exhibited symptoms of ANCA-associated vasculitis after receiving one of these COVID-19 vaccines.

Specifically, 22 patients exhibited kidney damage, manifested as new-onset or recurrent glomerulonephritis. At least 24 individuals presented with hematuria. Ten experienced lung damage, with five cases involving alveolar hemorrhage. One person developed optic neuritis, and another had auricular chondritis. These are manifestations of organ damage following vaccine administration.

Most patients received immunosuppressive treatment, including steroid medications. Additionally, five underwent plasma exchange, and at least five patients continued to rely on dialysis at the last follow-up.

The study mentioned that mRNA vaccines may stimulate myeloid and dendritic cells to varying degrees, activating downstream pathways to generate autoinflammation. Furthermore, mRNA vaccines generate antiviral-neutralizing antibodies and activate CD8+ and CD4+ T cells, triggering strong immune responses. Compared to natural infection, mRNA vaccines may enhance innate and acquired immunity stimulation. In some individuals with compromised immune systems, the ability to clear nucleic acids may decrease, potentially impacting neutrophils.

Vasculitis May Lead to Multiorgan Damage

There are different types of ANCA-associated vasculitis, including microscopic polyangiitis, where the frequency of MPO-ANCA positivity is notably high.

According to data from the Japan Intractable Diseases Information Center, approximately 70 percent of patients with microscopic polyangiitis experience systemic symptoms, including fever, weight loss, and fatigue. Additionally, symptoms such as hemorrhage, ischemia, or infarction in body tissues may occur.
Necrotizing glomerulonephritis is the most common, presenting with symptoms like hematuria, protein in urine, and elevated serum creatinine.

Early diagnosis is crucial, as the condition often progresses rapidly to kidney failure within weeks to months. Other prevalent manifestations include rash, with livedo reticularis, purpura, skin ulcers, and subcutaneous nodules in approximately 60 percent of patients with necrotizing glomerulonephritis. Polyneuropathy is observed in about 60 percent, joint pain in around 50 percent, and muscle pain in roughly 50 percent of cases.

Additionally, interstitial pneumonia is seen in approximately 25 percent, and alveolar hemorrhage in about 10 percent. Both conditions are attributed to vasculitis affecting the pulmonary capillaries, leading to cough, shortness of breath, rapid breathing, coughing up blood, bloody sputum, and severely low blood oxygen levels. Gastrointestinal involvement occurs in around 20 percent of cases, and myocardial involvement resulting in heart failure occurs in approximately 18 percent.

ANCA-associated vasculitis can be life-threatening if not promptly treated. Early diagnosis and appropriate treatment lead to improvement in the majority of cases. However, delayed treatment or poor response to initial therapy may result in irreversible organ dysfunction, necessitating procedures such as blood dialysis for patients experiencing kidney failure. Moreover, due to the possibility of symptom recurrence, patients should undergo regular checkups with specialists.

https://www.theepochtimes.com/health/covid-vaccines-could-trigger-vasculitis-damaging-multiple-organs-5563233

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Senator Rand Paul Says Dr. Anthony Fauci “Should Go to Prison”

Senator Rand Paul and Dr. Anthony Fauci have a history. The senator from Kentucky has grilled the former chief medical advisor to the president and head of the National Institute of Allergy and Infectious Diseases (NIAID) multiple times. Paul has questioned Fauci over everything from royalties to the National Institutes of Health (NIH) for research grants and questioning the former NIAID head about the validity and vaccine risks of Covid boosters for children. Senator Paul has gone as far as writing a letter to the Department of Justice accusing Fauci of perjury. Paul claims Fauci lied to Congress regarding funding for the Wuhan Lab in China. Now, the senator is claiming Fauci deserves to go to prison.

Paul says Fauci is “dishonest”

“For his dishonesty, frankly, he should go to prison,” said Paul in an interview. “Do you think the scientific knowledge that was gained from this research was worth the deaths of 20 million people?” In June of 2023, the Government Accountability Office issued a report that said the NIH had contributed more than $1.4 million to Chinese research institutions between 2014 and 2019, in spite of biosafety concerns. This included the Wuhan Lab. Fauci denied, in testimony to Congress, the NIH-funded gain of function research in China.

Paul is astounded Democrats still treat Fauci as a “medical messiah” and protect him. Paul believes Fauci is a “symbol of big government.” “He’s never been held responsible,” says Paul. The senator added, “History should judge him as a deficient person who made one of the worst decisions in public health history — in the entire history of the world.” For his part, Anthony Fauci responded by saying putting him in jail is “irresponsible,” and he doesn’t have a response to this “craziness.” “I mean, prosecute me for what? What are they talking about? I mean, I wish I could figure out what the heck they were talking about. I think they’re just going off the deep end.”

Fauci “Doesn’t Recall”

In early January, Fauci testified in front of the House Select Subcommittee on the Coronavirus Pandemic. Fauci’s testimony was behind closed doors, but Congressman Brad Wenstrup (R-Ohio), chairman of the subcommittee, said in a statement after the first day of testimony the interview had uncovered “drastic and systemic failures in America’s public health systems.”

The chairman was also surprised by how much Fauci said he “doesn’t recall” about the early days of the Covid outbreak. Senator Paul jumped on the fact Fauci couldn’t recall. “A guy that’s smart enough to think that he can shut down the schools, shut down the economy, force everybody to get vaccinated, including children, including people who have already had COVID, including the military – we had mandates everywhere, and he was all for them – yet he can’t recall how the decision-making went or what the science is to support this,” Paul said.

Wenstrup’s statement added, “Dr. Fauci’s transcribed interview revealed systemic failures in our public health system and shed light on serious procedural concerns with our public health authority. It is clear that dissenting opinions were often not considered or suppressed completely. Should a future pandemic arise, America’s response must be guided by scientific facts and conclusive data.”

During the pandemic TrialSite came across various documents and artifacts that certainly contributes to the evidentiary weight of the lab leak hypothesis. According to interactions with the Department of Defense’s research arm (DARPA), they could not deny a memorandum summarizing the American origin of SARS-CoV-2. In an email interaction the head of communications for DARAP informed TrialSite while they could not verify or deny the veracity of the memo they could go on the record that they were not funding EcoHealth Alliance, the nonprofit that Fauci has a record of helping to fund. Of course, EcoHealth Alliance served as a way to outsource what was likely gain-of-function research to the Wuhan Institute of Virology.

How could Fauci not know?

Author Says US Needs a “Pentagon” for Diseases

Donald G. McNeil, Jr., the author of “The Wisdom of Plagues: Lessons from 25 Years of Covering Pandemics,” claims what is needed now is a Pentagon for disease. “I’ve reported on pandemics and plagues for nearly three decades in over 60 nations, and one thing has become unquestionably clear: our greatest flaw in the battle against disease is that, below the president, no one is in charge.” McNeil points out when a pandemic occurs too often it “becomes mired in denialism, fatalism, bigotry, rumormongering, profiteering and partisan politics.”

McNeil goes further by saying there is no provision in the Constitution for Health. Too often, it’s left to local governments and private industry. According to McNeil, private industry needs to be incentivized but also has to be reined in so it doesn’t prioritize profits over people’s lives. Also, hospitals have to be reorganized, resources have to be moved to the front lines, and McNeil advocates for the drafting of doctors. Additionally, the author says the director of the Centers for Disease Control (CDC) should not be a political appointee. But McNeil adds, given the polarization of the United States he “despairs” about the country’s ability to adopt new thinking.

https://www.trialsitenews.com/a/senator-rand-paul-says-dr.-anthony-fauci-should-go-to-prison-2d785b15

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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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Injuries and Deaths Associated With the Very First Vaccines

Injurious side-effects were not always rare

This is Part 3 in the series “Revisiting the Historical Vaccines”
In this series, we will explore the multifaceted history of vaccines, examine historical data, and seek a nuanced understanding of vaccine efficacy and safety.

Deaths and injuries linked to vaccines were not only observed after the mass COVID-19 vaccination. There are records of severe adverse events since the first vaccines in human history were developed.

Deaths and Severe Injuries After Vaccination

The journey of smallpox vaccination, dating back to the late 18th century, is marred by numerous accounts of adverse effects and complications. Severe complications such as progressive vaccinia, an infection resulting from the vaccine virus itself, eczema vaccinatum, and encephalitis were rare yet grave adverse effects.
Official records from England from 1859 to 1921, as documented by J.T. Biggs in the 1912 book “Leicester: Sanitation versus Vaccination,“ reveal the disconcerting trend of vaccination-related complications that led to approximately 1,530 deaths directly attributed to the smallpox vaccine.

Notably, in the period from 1906 to 1922, the mortality rates from both smallpox and vaccination-related deaths were alarmingly similar.

The table, sourced from the Annual Returns of the Registrar-General, as recorded in Biggs’ book, was considered an indicator rather than a comprehensive record, omitting permanent or severe injuries.

It is well noted in the table above that due to the enforcement of vaccination, the nomenclature of the adverse events post-vaccination was limited to “cowpox” from 1898 through 1910. The causality of the smallpox vaccine in these death cases was further strengthened by a report in 1897 referring to the 36 deaths reported for that year as directly attributed to the effects of vaccination. Furthermore, the cause of death was either clearly stated in the medical certificate or was confirmed by investigation.

In June 1902, Dr. W. J. J. Stewart reported that out of 587 vaccinated men at Gore Farm Lower Hospital, over 28 percent ended up on sick leave as a result of vaccination, a significant finding not publicly disclosed. These individuals received public sick pay, and contractors were compensated for their loss of services.

“Fresh vesicles subsequently formed around the vaccination pocks coalescing with them and causing them to spread. They also developed on the face, head, body, and in the mouth; the [latter] prevented the child from suckling, and it died exhausted on the 45th day after vaccination. (Case of a healthy child after vaccination, March 13, 1891.)” This child was likely to die of a progressive form of disease following the vaccination.

The vaccine’s potential to cause serious harm was further underscored by specific cases of erysipelas, a severe form of skin infection resulting in a painful and prolonged death. Instances included a 13-week-old infant succumbing to “general erysipelas after vaccination” and a 4-month-old girl dying from the same condition post-vaccination. These cases were not isolated incidents but were part of a broader pattern of severe reactions to the smallpox vaccine, likely caused by the numerous pathogens the vaccine carried that led to severe skin infections.

Eczema vaccinatum, another serious condition linked to the vaccine, presented further evidence of the risks associated with smallpox immunization. In one case, a 15-month-old boy tragically died after developing this condition following his vaccination. This was likely caused by the inflammatory cytokines in those so-called “pure lymph” or other types of smallpox vaccines.

Encephalitis following vaccination, though uncommon, often results in fatalities, particularly in babies and young children. The death rate in reported cases varies between 9 to 40 percent. Unfortunately, 10 to 25 percent of those who survive this condition suffer from lasting neurological damage.

A 2003 systematic review of the risk for serious complications and death from smallpox vaccination in the United States from 1963 to 1968 found post-vaccinial encephalitis and vaccinia necrosum had life-threatening complication rates of at least 3 per million and 1 per million primary vaccinations, respectively. The death rate was 29 percent for post-vaccinial encephalitis and 15 percent for vaccinia necrosum cases.

Similar to smallpox vaccine failures, current COVID-19 “vaccine” issues involve adverse effects that are also closely linked to the components of the vaccine, including blood clots, brain bleeds, myocarditis, pericarditis, aggressive cancers, and autoimmune diseases.

‘The Heighth of Absurdity’

In a 1900 letter to the editor of “The Medical Brief,” Dr. Harman, a medical doctor, stated that introducing cowpox poison into the bloodstream of a healthy person was not only flawed logic but risky. “It would be the heighth of absurdity” to administer medicine to a person in good health and claim to prevent a disease they did not contract, he said.

The book ”The Value of Vaccination: A Non-Partisan Review of Its History and Results“ by Dr. George William Winterburn cited the following report from the March 4, 1882, Washington National Board of Health Bulletin:

“Our town authorities have employed a physician to vaccinate all persons who present themselves for the purpose.

“The result has been fearful. Nearly everyone vaccinated has suffered from Erythema or Erysipelas, the arms swollen from shoulder to wrist, and the point of puncture [where the person was vaccinated] presenting the appearance of sloughing ulcer [a separation of dead from living tissue], discharging freely sanious pus [blood and pus]. Many of the sufferers have been confined to bed, with high fever, from five to ten days, requiring the constant application of poultices [medicated treatment] to the arm, and the free use of morphia [morphine] for the relief of pain.

“Those who have tried it tell me they would much prefer to have smallpox.”

Ladies Played a Role

Regardless of the controversies over the effectiveness and safety of the smallpox vaccines, the vaccines were forced upon healthy people anyway. The first campaign for global smallpox vaccination took place from 1803 to 1813.

Smallpox was not only the most significant cause of blindness in the population, but it also left survivors with pockmarks. These physical aftereffects were particularly significant for women, as societal norms at the time placed a high value on a woman’s appearance. Smallpox scars could seriously diminish a young woman’s prospects for marriage, which was a critical aspect of a woman’s social and economic stability during that period.

The article “Jenner’s Ladies: Women and Vaccination against Smallpox in Early Nineteenth-Century Britain” by Michael Bennett highlights the significant role played by women in making vaccination fashionable and widely accepted in the early 19th century. They sponsored and encouraged vaccination through voluntary societies and used their influence in their respective spheres to promote this new prophylactic.

For example, Mrs. Bayley of Hope Hall near Manchester made a notable contribution by vaccinating the poor and offering a monetary reward to anyone who caught smallpox after her vaccinations.

In another instance, Dr. Lettsom highlighted that “ladies of rank” had vaccinated 30,000 children by the end of 1805. This is an aspect of medical history that has not been extensively studied.

Leicester Opposition

Although claimed to be infrequent, these complications presented a significant challenge in the widespread acceptance and administration of the vaccine.

The English government began enforcing mandated smallpox vaccination in the mid-19th century, specifically 1840 and 1853.

Despite high vaccination rates, a severe smallpox epidemic struck in the small manufacturing town of Leicester and other parts of England in the early 1870s, resulting in 3,000 cases and 358 deaths in Leicester alone. This led to public skepticism about the efficacy of vaccination, as reflected in an 1884 letter published in the Leicester Mercury newspaper.

Contradictorily, the government intensified its vaccination efforts, employing officers to prosecute those refusing to vaccinate their children. Opposition to vaccination was fueled by numerous instances of severe health complications and fatalities following vaccination. One notable case involved Arthur Ward, whose two children were harmed by vaccination; he refused further vaccination for his other child and faced legal penalties.

Despite serious health risks, the government’s unwavering support for mandatory vaccination spurred widespread revolt. Thousands protested in Leicester, drawing participants from various English countries and diverse professions. The demonstration was grand, with music, banners, and flags bearing messages championing liberty and criticizing vaccination. The procession, stretching 2 miles, received enthusiastic support from townspeople.

The scale of the protest, with attendance estimated between 80,000 to 100,000, signified a major public stance against compulsory vaccination. The event was led by Mr. Councillor Butcher of Leicester and included speeches and resolutions advocating personal liberty and parental rights. An evening meeting, attended by delegates from over 60 towns, further solidified the demonstration’s success.

Dr. Spencer T. Hall, a senior participant, expressed profound joy at the challenges to vaccination. This historical event marked a significant moment in public health, where thousands courageously opposed a prevailing medical belief and stringent government regulations, advocating for self-determination in health decisions.

70 Years of Laboratory Manipulation

According to modern vaccine quality standards, there are valid reasons to question the safety and efficacy of the smallpox vaccine, which has been highly praised for eradicating smallpox. The precise components of the smallpox vaccines remain a mystery.
The modern smallpox vaccine has gone through three generations of development. The first and second generations of the vaccine, developed between the 1950s and 1970s, used original live viruses grown on animal skin or in cell cultures. These versions carried a higher risk of severe or life-threatening side effects, including 1 to 2 fatalities per million vaccinations, 3 to 9 cases of postvaccinal encephalitis, 1 to 7 instances of progressive vaccinia, and 2 to 35 cases of eczema vaccinatum.

Because the viruses contained in the smallpox vaccine were still alive, they had to be maintained in lab animals and cell cultures. People may not be aware that modern smallpox vaccines have a complex 70-year history of passage in various laboratory animals, including rabbits, mice, goats, and cows, to make the modern attenuated smallpox vaccines.

This may be the first example in human history of the initial types of laboratory manipulation of a virus later used for vaccination.

For example, the most widely used Dryvax vaccine was from calf lymph derived from the New York City Board of Health strain. Dryvax, a vaccine licensed in the United States, is a lyophilized (freeze-dried), live-virus preparation of the infectious vaccinia virus, which was thought to play a significant role in eradicating smallpox.

Third-generation vaccines utilized attenuated strains of vaccinia and had limited usage before smallpox eradication. These vaccines have relatively milder side effects due to weakened virus strains, replacing Dryvax.

A Complex ‘Broth’ of Viruses

In the late 1990s, when researchers studied the genetic components of vaccines via advanced gene sequencing tools, they discovered that Dryvax was far more complex than initially thought.

The study suggested that Dryvax was made up of many different viruses. The sequencing identified an evolving mutation pattern, with some genes highly fragmented and others disrupted in specific strains.

The study emphasized the significant complex nature of the Dryvax vaccine, highlighting the huge impact of human laboratory interventions on orthopoxvirus populations (viruses that cause poxvirus diseases such as smallpox, cowpox, and monkeypox).

Even modern smallpox vaccines do not contain cowpox or smallpox virus but are a hybrid human and animal agent that never existed in nature until the era of vaccination. This is similar to the story of COVID-19 and the profound impact of human research on the evolution of wild-type viruses, drawing parallels to the origin of the SARS-CoV-2 virus responsible for the COVID-19 pandemic.

The COVID-19 virus has far more advanced gene editing technologies responsible for the origin of the SARS-CoV-2, while the smallpox vaccine used a simpler method of virus culture.

Propagating a False Narrative

The smallpox vaccine has been described as a magical medical invention. However, a closer look at the historical data reveals a more nuanced story of the disease’s prevalence and mortality, as well as the impact of the vaccine.

Nevertheless, this narrative was devised over hundreds of years. Propagating such a narrative is easier when there’s limited access to historical documentation of deaths and injuries after smallpox vaccination. This has made examining the causal relationships between the natural smallpox waves and the vaccination campaigns nearly impossible.

People also tend to trust public health authorities who have made this the official narrative. We have the same problem today with the COVID-19 narrative, which has been easier to propagate with control over the media.

https://www.theepochtimes.com/health/injuries-and-deaths-associated-with-the-very-first-vaccines-5541947

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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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A pandemic mea culpa from Francis Collins

IT COMES three years too late. But Francis Collins, the former head of the National Institutes of Health, has finally admitted that the COVID-19 lockdowns caused a massive amount of harm — harm to which he and other government public-health experts, such as Anthony Fauci of the National Institute of Allergy and Infectious Diseases, were oblivious because they were obsessed with doing things their way.

The mea culpa came last summer during a conversation hosted by Braver Angels, an organization that promotes dialogue among Americans with sharply different ideologies and political loyalties. Collins, who as NIH director played a central role in shaping Washington's response to COVID-19, was paired with Wilk Wilkinson, a Minnesota trucking manager and podcast host who strongly opposed how government officials addressed the pandemic. The 90-minute exchange, moderated by Boston College professor Martha Bayles, was recorded six months ago but only recently attracted attention when excerpts were posted on social media.

The whole conversation was interesting, but one segment in particular was jaw-dropping. Collins described with remarkable candor just how narrow-minded, how willfully myopic, he and other high-level public health officials had been as they dealt with the crisis.

"As a guy living inside the Beltway, feeling the sense of crisis, trying to decide what to do in some situation room in the White House with people who had data that was incomplete, we weren't really thinking about what that would mean to Wilk and his family in Minnesota a thousand miles away from where the virus was hitting so hard," confessed Collins, who retired from the NIH at the end of 2021. "We weren't really considering the consequences in communities that were not New York City or some other big city."

That was a stunning admission. What he said next was even more scandalous.

"If you're a public health person and you're trying to make a decision, you have this very narrow view of what the right decision is, and that is something that will save a life. Doesn't matter what else happens. So you attach infinite value to stopping the disease and saving a life. You attach zero value to whether this actually totally disrupts people's lives, ruins the economy, and has many kids kept out of school in a way that they never recover from."

"Collateral damage," said Wilkinson.

"Collateral damage," Collins agreed. He and his colleagues were locked in what he now concedes was the "public health mindset" — a monomaniacal approach that blinded them to the injuries they were causing. "A lot of us had that mindset, and that was really unfortunate."

Was it ever.

As early as March 2020, Fauci recommended a nationwide lockdown and called for a "dramatic diminution of the personal interaction" in daily activities. He warned that "life is not going to be the way it used to be in the United States," while insisting that was "best for the American public." Collins said at the time that the only correct approach was "one that most people would find to be too drastic because otherwise it is not drastic enough."

Now, of course, it is far too late to mitigate any of the pain endured by millions of Americans hurt by the government's high-handed edicts and recommendations. Those curbs and controls began with the declaration of a federal emergency and travel ban, which in turn spurred many states to order their own restrictions.

The coast-to-coast lockdown destroyed tens of millions of jobs and at least 200,000 small businesses. It exacerbated numerous social ills, worsened mental illness, and took a deadly toll in missed cancer diagnoses and untreated heart disease. The prolonged school closures inflicted unprecedented damage on children. The social distancing and mask mandates were enforced with a ruthlessness that at times turned despotic. And countless men and women — from ordinary citizens to noted epidemiologists to elected state officials — found themselves demonized, censored, or shunned for challenging those who attached "zero value" to their concerns.

All this damage was caused not by the pandemic but by politicians who abdicated their judgment and left it to public-health experts. Whether out of panic, pigheadedness, or perversity, they declined to balance costs against benefits, a basic function of policymaking. Instead, they insisted they would "follow the science" — as though scientists were endowed with an infallible road map to navigate COVID's complex interplay of disease, economics, education, psychology, and politics in a nation of 330 million people.

The great economist and social historian Thomas Sowell has often observed that "there are no solutions, there are only tradeoffs." That is a fundamental reality in all policymaking. There are pros and cons to everything government does. For officials responding to the pandemic, there can hardly have been a more shocking intellectual failure than the one to which Collins now confesses: attaching "infinite value" to stopping the disease and no value at all to everything else.

The same sort of thinking can be a pitfall in many other areas. Focus on reducing fossil fuel use at any price, for example, and the results will be stunted economic growth and continued misery for many of the world's poorest people. Assign maximum importance to achieving racial diversity in student admissions and the result is affirmative action preferences so lopsided that they violate the Constitution. Allow the prevention of another 9/11 to override every other consideration, and the CIA ends up torturing prisoners in secret "black sites" beyond the reach of law.

From crime to homelessness to addiction to national defense, there are always costs to be weighed against benefits. And if acknowledging tradeoffs is indispensable to the work of government, it is especially so at times of crisis.

Toward the end of the Braver Angels conversation, Collins acknowledged another way in which he and many of his inside-the-Beltway colleagues blundered.

It was folly, he said, to think that Washington knew what was best for the whole nation. "The fact that we could put blanket recommendations across this incredible wide, broad, and diverse country and expect them to be right . . . obviously could not have been correct. And yet that's what was done."

COVID-19 would have been a terrible destroyer in any case. But it was made all the more catastrophic by the failure of politicians and experts who not only were sure they knew best but were unwilling even to consider other views. Americans' respect for public-health experts took a beating during the pandemic, and it is a black mark on Collins's legacy that he was so complacent about the harm the government's policies caused. For belatedly admitting where he went wrong, he certainly deserves credit. Let him continue to speak out, to warn other scientists against falling into the same trap, and he'll deserve a lot more.

https://jeffjacoby.com/27499/a-pandemic-mea-culpa-from-francis-collins

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UK Covid Inquiry Put on Hold

The Covid Inquiry in the United Kingdom initially looked like it was going to be just “window dressing”. The Inquiry, which began at the end of May in 2023, as an independent public investigation with many of the government ministers wanting trying to stop or dodge questioning. The Inquiry is headed by Baroness Heather Hallett, a former Court of Appeal Judge. The important aspect of the Inquiry is that it exists. In December of last year, alternative viewpoints to Covid and the vaccine were heard along with politicians, specifically testimony from former Prime Minister Boris Johnson. Johnson admitted mistakes in his handling of the pandemic but that he did his “level best” at the time. Now, it appears the UK Covid Inquiry is on “hold.”

Public Hearings Postponed

Last week, the UK COVID-19 Inquiry issued a statement formally announcing the Inquiry will be “rescheduled”. The hearings were scheduled to take place in the summer of 2024, but will now happen at a later date to allow organizations time to “prioritize” their materials for the inquiry’s third investigation on the impact of the pandemic.

Baroness Hallet, the chair of the Inquiry, said she knows people are disappointed with the postponement but said more time was needed to prepare for a separate investigation on how the pandemic impacted the British National Health Service (NHS). "I want to ensure our hearings in 2024 are as effective as possible and I recognize the increasing pressure on organizations to respond to requests and provide information to the inquiry," the Baroness said. "I remain committed to not allowing the inquiry hearings to run beyond my original aim of summer 2026," she added.

Different “Phases”

The UK Covid Inquiry has been split up into different phases. The first phase, which started in 2023, was set up to gather evidence in the planning for the pandemic. The findings and recommendations of this phase are due this summer. The second phase is looking at how political decisions were made after the Covid pandemic hit Britain. The second phase started in London in October of 2023, and will travel to the rest of the UK to collect evidence.

Public hearings will start again this September, to look at the impact the pandemic had on the NHS. There is also an investigation into vaccines which will cover the safety of the Covid jabs and the link between the serums and heart ailments. The investigation will cover whether reforms are needed. No timetable has been set for the return of the hearings, but the Inquiry has promised more details in the “coming weeks.”

Politics

The political implications of the Inquiry could influence the next election in Britain. First, Simon Case, the current cabinet secretary for the Conservative government, is expected to testify in a special hearing in the spring. Reportedly, Case was critical of British ministers during the pandemic and had said former Prime Minister Boris Johnson was “unable to lead.” Second, the publication of the independent Inquiry could cause election problems for British Prime Minister Rishi Sunak. The findings could reveal how the government was obsessed with Brexit and the pandemic was downplayed.

Already, former ministers have criticized the UK Covid Inquiry. Former Health Minister Lord Bethell complained the investigation was too focused on “office tittle tattle”. Reportedly, Bethell was involved in negotiating “controversial contracts.”

Rivka Gottlieb, a spokesperson for the COVID-19 Bereaved Families, UK said, the Inquiry’s findings “must be released as soon as possible so they can be put into action to protect us from a future pandemic.” Unfortunately for those most in need, such as individuals struggling with injuries or long COVID it will likely be too little too late, in other words, window dressing.

https://www.trialsitenews.com/a/uk-covid-inquiry-put-on-hold-2d0bb420

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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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Ask Why 429 Moms Died

“U.S. maternal deaths are on a worrisome trajectory,” the American Medical Association declared after news that pregnancy-related deaths soared 40 percent in 2021 to levels unseen since 1965.

But in releasing its 2021 maternal mortality report—seventeen months after the fact—the U.S. Centers for Disease Control left out crucial context. It made no mention of the role of Covid-19, even in the pandemic’s worst year and even as data was readily available.

We analyzed that data, assisted by a programmer and an actuary, and found a disturbing trend. Of the 1,205 mothers who died in or within forty-two days of pregnancy in 2021, 429 had Covid-19 on the death certificate as either the primary or a contributing cause—a 321 percent increase in Covid pregnancy deaths from the first wave in 2020. By comparison, total Covid deaths in the United States rose a relatively modest 20 percent—one-fifteen as much as in pregnant women.

Such a huge disparity suggests that Covid, which typically claims the elderly and medically compromised, did not solely drive these pregnancy deaths. Rather, the campaign to vaccinate pregnant women in the heat of the second Covid wave may have combined to make infections worse in the vaccinated. The phenomenon, often minimized as “breakthrough infection,” is called vaccine-associated enhanced disease or VAED and has been documented in measles, respiratory syncytial virus, and dengue fever.

The 429 women who died from pregnancy-related Covid in 2021 are a tiny fraction of those who birthed 3.6 million babies in 2021. But their role in the nation’s 40 percent increase in maternal deaths deserves official scrutiny. When we looked at deaths of women for whom Covid was the prime killer—the underlying cause—we found an increase of 2,000 percent, from 16 mothers who died in 2020 to 335 in 2021.

Since the rollout of Covid vaccines in late 2020, a concerted effort has been made to minimize vaccine failures of efficacy and safety while overstating vaccine success. We contend that this awful chapter in Covid history, when more than 400 families lost wives and mothers, is instructive. It may also offer insight into vaccine-driven sickness and death in the general population that has been studiously ignored.

“All cases of vaccine failure should be investigated for VAED,” said a 2021 article in the journal Vaccine on Covid-19 vaccines.

Clearly, that is not happening.

Pregnant Women Excluded

In the spring and summer of 2021, pregnant women were repeatedly urged to protect themselves and their babies by taking Covid vaccinations, with website and social media depictions of smiling mothers holding their blossoming bellies. CDC did this knowing that supporting data was spare.

“Pregnant women were excluded from COVID-19 vaccine clinical trials and thus data to date on safety of COVID-19 vaccines in pregnancy is limited,” a CDC proposal to monitor safety reads from June 2021. There is “an urgent need for outcome data following [emphasis added] use of COVID-19 vaccines in pregnant populations.”

Although the vaccines were still under “emergency use authorization,” which is well short of formal approval, the CDC on April 23, 2021, first encouraged and on August 11, 2021, urged Covid vaccination before, during, and after pregnancy. The American College of Obstetricians and Gynecologists got on board on July 30, 2021.

For the first time in history women were exhorted—some were mandated by employers—to take a novel, minimally tested, injected pharmaceutical even in the sacrosanct first trimester of fetal development. Yet the CDC endorsements referred to research only in third-trimester vaccination. This includes a study of 827 pregnancies that found normal rates of miscarriage but inexplicably included 700 women who were vaccinated after 20 weeks, when fetal losses are not characterized as miscarriages.

Lacking robust safety data, the CDC was acting on published reports of serious illness and deaths of pregnant women from Covid, which some studies found was higher and others equal or lower. But while the vaccination campaign was supposed to lead to fewer deaths, more women died than in pre-vaccination 2020 and at rates higher than the general population, our study found.

‘Enhanced’ Disease Dismissed

By August 7, 2021, 48 percent of pregnant women had been inoculated, including 22 percent during pregnancy. Half of the 2021 Covid-in-pregnancy deaths in our data occurred in August and September, coinciding both with advisories to vaccinate and the Delta wave—perfect conditions for enhanced disease. Blaming Delta for the maternal deaths is an incomplete explanation. The Delta wave was indisputably difficult among other groups; Covid deaths of 18- to 49-year-olds, for example, rose 147 percent from 2020 to 2021, we found. But the government chose to vaccinate our way out of Covid. Successive waves suggest that approach—applied even to people with infection-induced natural immunity—failed.
Moreover, the vaccine program may even have driven up Covid cases and Covid mortality. Pfizer’s own documents, released under a court order and studied by the Daily Clout, point in this direction.

In the first ninety days of the rollout, Pfizer researchers recorded 2,585 cases of vaccinees whose “serious adverse event” was actually Covid-19 itself, the Daily Clout reported. Of those cases, 136 people died (and 2,110 had “unknown” outcomes), the Pfizer documents show.

“These cases are very suggestive of VAEDS,” three physicians who analyzed Pfizer reports for Daily Clout told us in an emailed statement. Yet Pfizer claimed that none of the cases, including in seventy-five vaccinees with “severe” disease, “could be definitively considered” as vaccine influenced. The physicians, Joseph Gehrett, Barbara Gehrett, and Chris Flowers, called VAEDS “an unattainable diagnosis…almost impossible” to meet under the current definition applied to Covid.

Asked about our findings, the physicians commented, “If a large proportion of the 2021 maternal deaths from COVID-19 occurred in vaccinated women, it would be highly suspicious for probable or possible VAED and should be aggressively investigated.”

Testament to the issue’s lack of urgency, a CDC study of what it called vaccine-mediated enhanced disease in Covid, launched in June 2021, has not reported results more than thirty months later. An agency spokesman said research concluded six weeks ago and is undergoing peer review.

In 2022, after the Omicron variant took over and vaccinations slowed, eighty-eight women died from Covid in or within forty-two days of pregnancy, about one-fourth the number of 2021. Erased was the 40 percent increase in maternal mortality of a year earlier.

Pandemic’s Darkest Time

Clearly, the pandemic was a turning point in the use of new pharmaceuticals in pregnancy. Barriers fell, and so did caution.

The new drug remdesivir, sold as Veklury, was given to hospitalized pregnant women with Covid, first under emergency use authorization in 2020. Yet the package insert—similar to those for mRNA vaccines—still stipulates, “There are insufficient human data on the use of Veklury during pregnancy.”

Dr. Peter A. McCullough, a published cardiologist who first warned of post-vaccine myocarditis, told us, “I am very concerned that antecedent or gestational administration of COVID-19 vaccines is associated with maternal death.” The virus and vaccine together, as he put it, can “super-load” the body with dangerous spike proteins from each. CDC should focus on these pregnancy outcomes, he proposes, by merging vaccine and mortality data, which is often out of researchers’ reach.

The third quarter of 2021, when maternal deaths peaked, is infamous for the start of another worrisome trend, first reported by OneAmerica insurance company, of a 40 percent increase in deaths among 18- to 64-year-olds. “We are seeing, right now, the highest death rates we have seen in the history of this business—not just at OneAmerica,” CEO Scott Davison said then.

Similarly, actuarial data shows excess deaths soared then among insured working-age adults—with double the mortality, for example, in 35- to 44-year-olds from the pre-pandemic norm. This trend continues even now and cannot be fully explained by Covid. Nor can a 33 percent rise since 2020 in the number of disabled Americans. Yet the government has shown little inclination to study this catastrophic toll of early death and infirmity.

Excess deaths, disability rolls, and maternal mortality numbers are trying to tell us something. They should be heeded.

https://www.trialsitenews.com/a/ask-why-429-moms-died-a305d67b

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Autopsy Findings in Cases of Fatal COVID-19 Vaccine-Induced Myocarditis

The American College of Cardiology in 2022, with an unprecedented position statement on an illness outside of their field, published the ACC Expert Consensus Decision Pathway on Cardiovascular Sequelae of COVID-19 in Adults, and in that document stated, “The ACC has long supported vaccination as a vital protective measure against dangerous illness and for personal and community health. There is no question that the benefits of COVID-19 vaccination generally outweigh the risks.”

Now, a paper peer-reviewed and published today should make every cardiologist question their support of COVID-19 vaccination with the reality that some patients have died with myocarditis sacrificing their lives for a vaccine without randomized trial data demonstrating reductions in viral transmission or adjudicated COVID-19 hospitalization, death or any hard outcome. The dangerous ACC proposition based on a false premise has eroded: “COVID-19 illness causes more myocarditis than the vaccine, so we should vaccinate patients” and therefore, cause MORE and FATAL myocarditis! No reasonable and prudent doctor could practice with this perverse rationalization.

Hulscher et al. published in the European Society of Cardiology Heart Failure a report on 28 cases of COVID-19 vaccine-induced myocarditis and concluded based on the pathologic findings that death was caused by the injection. Without vaccination, these patients with an average age of 44 would be alive today. They also conclude using the Bradford-Hill criteria, that cardiac death after vaccination can be inferred using epidemiological criteria, in other words, unexplained cardiovascular deaths in the vaccinated with no prior antecedent disease are likely caused by vaccination.

I expect the Bio-Pharmaceutical Complex to exert tremendous pressure on Wiley the publisher and the journal to retract the paper in violation of the COPE (Committee on Publication Ethics) guidelines. This has occurred numerous times during the pandemic as a form of medical censorship when valid papers are published demonstrating the fatal harms of COVID-19 vaccination. To be prepared, here are the COPE criteria:

Editors should consider retracting a publication if:

They have clear evidence that the findings are unreliable, either as a result of major error (eg, miscalculation or experimental error), or as a result of fabrication (eg, of data) or falsification (eg, image manipulation)

It constitutes plagiarism

The findings have previously been published elsewhere without proper attribution to previous sources or disclosure to the editor, permission to republish, or justification (ie, cases of redundant publication)

It contains material or data without authorization for use

Copyright has been infringed or there is some other serious legal issue (eg, libel, privacy)

It reports unethical research

It has been published solely on the basis of a compromised or manipulated peer review process

The author(s) failed to disclose a major competing interest (a.k.a. conflict of interest) that, in the view of the editor, would have unduly affected interpretations of the work or recommendations by editors and peer reviewers.

We have taken every step to ensure none of these criteria could be met for this paper. In my view, the most important figure in the paper demonstrates how large numbers of vaccine deaths are occurring among young people otherwise known as “sudden adult death syndrome.”

Hulscher N, Hodkinson R, Makis W, McCullough PA. Autopsy findings in cases of fatal COVID-19 vaccine-induced myocarditis. ESC Heart Fail. 2024 Jan 14. doi: 10.1002/ehf2.14680. Epub ahead of print. PMID: 38221509.

https://www.trialsitenews.com/a/breaking-peer-reviewed-published-autopsy-findings-in-cases-of-fatal-covid-19-vaccine-induced-myocarditis-852f1a95

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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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Cardiovascular Autonomic Dysfunction at Crisis Levels in Long COVID Patients

A group of cardiovascular-focused expert researchers spanning the United States, Canada, United Kingdom, Austria and Sweden investigate cardiovascular autonomic dysfunction (CVAD), a malfunction of the cardiovascular system triggered by deranged autonomic control of circulatory homeostasis. CVAD is a malfunction of the cardiovascular system caused by deranged autonomic control of circulatory homeostasis. CVAD is an important component of post-COVID-19 syndrome, also termed long COVID, and might affect one-third of highly symptomatic patients with COVID-19.

With effects present throughout the whole body, prominent observations include impairment of heart rate and blood pressure control, plus manifestation in specific body regions; for example, manifesting as microvascular dysfunction.

Corresponding author Arthur Fedorowski, M.D., Ph.D., a notable cardiology specialist-investigator with Karolinska University Hospital, as well as Lund University and colleagues, report long COVID patients meeting severe conditions “meet the diagnostic criteria for two common presentations of CVAD” including:

1) postural orthostatic tachycardia syndrome

2) inappropriate sinus tachycardia.

Other related CVAD-linked conditions are associated with hypotension, such as orthostatic or postprandial hypotension, and recurrent reflex syncope.

Any Research Breakthroughs?

Fedorowski and colleagues point out that the pandemic did manage to accelerate long COVID research investigation helping to identify “new potential pathophysiological mechanisms, diagnostic methods and therapeutic targets in CVAD.”

The clinician/specialist-scientists point to the need for clinicians in the field who may encounter patients with CVAD on a daily basis and point out that more important than ever is “knowledge of its symptomatology, detection and appropriate management.”

Findings

Summarizing the recent medical literature research review in the journal Nature, the cardiology-centered researchers both establish a working definition based on the unfolding long COVID dynamic not to mention delineate the condition’s major forms presently reported on in lost COVID-19 syndrome patients.

Describing etiologies

In this review, we define CVAD and its major forms that are encountered in post-COVID-19 syndrome and describe possible CVAD etiologies (cause of disease) the cardiovascular-focused collaboration seeks to establish a more detailed linking of CVAD and post-COVID-19 syndrome or long COVID.

The goal obviously is to help empower more clinicians to both diagnose and manage this unfolding situation, plus delineate a research trajectory with an aim of a more efficient treatment pathway to address the ever more prevalent and enduring medical condition.

https://www.trialsitenews.com/a/cardiovascular-autonomic-dysfunction-at-crisis-levels-in-long-covid-patients-86042fa9

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Japanese Vaccine Study Group Holds Press Release Six Months After Launch—Pervasive Safety Problems with MRNA COVID-19 Vaccines

Japan was the scene of a press conference for the General Incorporated Association Vaccine Issues Study Group in that Asian nation of 125.7 million, and the world’s third largest economy as measured by gross domestic product. A major pharmaceutical market, the Japanese group’s January 11, 2024, event centered around a concerted, systematic review of the medical literature covering COVID-19 vaccines. Professor Emeritus Masanori Fukushima, M.D., Ph.D., from Kyoto University cites the database of studies made possible by patient advocacy group React19 along with the TrialSite partnership to continuously promote the existence of a large body of peer-reviewed medical literature tracking adverse side effects, some of them injury causes, associated to the COVID-19 countermeasure program. The Japanese event occurred January 11, 2024.

The COVID-19 vaccines side effects can adversely impact every organ across the human body as more data supports the spike protein hypothesis. That is, that the mRNA induced spike protein can persist and travel in the human body for not only weeks, but months and even years.

Apparently, Japanese volunteer physicians have been amassing their own study hub, a set of documents derived from peer review case studies to more comprehensive population studies.

Substacker Aussie17 circulated the video snippet across the internet but few media picked up the event.

Ongoing medical censorship, according to the press conference, hinders physicians attempting to find ways to collaborate and care for patients. Then there’s the societal pressure, much like what we are experiencing in North America and Europe applying subtle and not so subtle pressure against any critical discussion about the COVID-19 vaccines, including vetting of mRNA-based vaccine injuries.

The participants also raised the specter of censorship at the level of scientific and medical journals, a phenomenon TrialSite has chronicled throughout the pandemic. TrialSite observed such censorship first with the discussion of alternative repurposed drugs such as ivermectin, then this same intuitive applied to critical discussion of the COVID-19 vaccines, or countermeasures as they are formally called by the U.S. government.

Professor Yasufumi Murakami went on the record at the event concerning adverse events, “One thing I want to say initially is that it is clear how the adverse effects occur, which is still holding many victims today. I believe it should be stopped immediately.”

Back to the spike protein hypothesis, not even acknowledged by the medical establishment in the developed nations, a mechanism of action now well understood, documented in multiple peer-reviewed studies and a recognition that the spike protein can at least in some cases circulate In the human body acting as an irritant with toxic impact.

Also problematic, at least for some patients, is the mRNA vaccines’ lipid nanoparticles (LNP), which can induce toxic reactions as well.

TrialSite reviewed and verified the General Incorporated “Association Vaccine Issues Study Group” and its press conference to discuss its report on six-month results.

Note that TrialSite includes multiple COVID-19 vaccine injury forums and publishes articles based on study after study suggesting government need for investment in ongoing investigation. Importantly many of the studies currently covering incidence involving side effects and the vaccine are case reviews, meaning they are not designed to establish causation.

Moreover, much dis-information and mis-information continues to circulate, especially from fringe groups claiming that the COVID-19 countermeasures were designed to specifically hurt people, such as part of a global cabal’s plan to depopulate the planet. This is dis-information and the more governments around the world withhold and suppress safety data the more these fringe groups benefit with an audience.

https://www.trialsitenews.com/a/japanese-association-vaccine-issues-study-group-holds-press-release-six-months-after-launchpervasive-safety-problems-with-mrna-covid-19-vaccines-63646b54

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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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How Moderna Came Up With a Vaccine Against Vaccine Dissent

Finances at the vaccine manufacturer Moderna began to fall almost as quickly as they had risen, as most Americans resisted getting yet another COVID booster shot. The pharmaceutical company, whose pioneering mRNA vaccine had turned it from small startup to biotech giant worth more than $100 billion in just a few years, reported a third-quarter loss last year of $3.6 billion, as most Americans refused to get another COVID booster shot.

In a September call aimed at shoring up investors, Moderna’s then-chief commercial officer, Arpa Garay, attributed some of the hesitancy pummeling Moderna’s numbers to uninformed vaccine skeptics. “Despite some misinformation,” Garay said, COVID-19 still drove significant hospitalizations. “It really is a vaccine that’s relevant across all age groups,” she insisted.

To get past the “misinformation” and convince the public to take continual booster shots, Garay briefly noted that Moderna was “delving down” on ways to partner “across the ecosystem to make sure consumers are educated on the need for the vaccine.”

What Garay hinted at during the call, but didn’t disclose, was that Moderna already had a sprawling media operation in place aimed at identifying and responding to critics of vaccine policy and the drug industry. A series of internal company reports and communications reviewed by RealClearInvestigations (RCI) show that Moderna has worked with former law enforcement and public health officials and a drug industry-funded non-governmental organization called The Public Good Projects (PGP) to confront the “root cause of vaccine hesitancy” by rapidly identifying and “shutting down misinformation.”

Part of this effort includes providing talking points to some 45,000 healthcare professionals “on how to respond when vaccine misinformation goes mainstream.” PGP and Moderna have created a new partnership, called the “Infodemic Training Program,” to prepare health care workers to respond to alleged vaccine-related misinformation.

The company has also used artificial intelligence to monitor millions of global online conversations to shape the contours of vaccine-related discussion. The internal files—shorthanded here as the Moderna Reports—show high-profile vaccine critics were closely monitored, particularly skeptics in independent media, including Michael Shellenberger, Russell Brand, and Alex Berenson. PGP, which was funded by a $1,275,000 donation from the Biotechnology and Innovation Organization, a lobby group representing Pfizer and Moderna, has identified alleged vaccine misinformation and helped facilitate the removal of content from Twitter, among other social media platforms, throughout 2021 and 2022.

Emails from that period show that PGP routinely sent Excel lists of accounts to amplify on Twitter and others to de-platform, including populist voices such as ZeroHedge.

The messages also suggested emerging narratives to remove from the platform. “People opposed to vaccines are capitalizing on the NYT [New York Times] article about the CDC withholding vaccine information. The articles do not contain misinformation themselves but are using the news to further prove the CDC is untrustworthy,” wrote Savannah Knell, PGP’s senior director of partnerships, in an email to a Twitter lobbyist in September 2022. In another email the following month, Kaitlyn Krizanic, PGP’s senior program manager, told Twitter to be on the lookout for “reports that Sweden is no longer recommending the vaccine for children.” In some cases, conservative accounts expressing outrage at restrictive pandemic policies, such as vaccination passports, were deemed by PGP as “misinformation” that warranted removal.

The Moderna Reports consistently show the company raising red flags about those reporting documented side effects of the vaccine the biotech company was selling. Such concerns, which may be typical of corporate public relations efforts that want their product shown in the best light, take on a darker cast when it involves medicine injected into people’s bodies.

Like the Twitter Files, the Moderna Reports highlight the push by powerful entities—especially government, Big Tech, and Big Pharma—to identify and brand dissenting opinions about establishment narratives as risky forms of speech. The growing network these efforts rely on shows the growth of what has been called the censorship industrial complex. Moderna’s faltering financials also suggest, at least for now, the limits of that project.

Public Good Projects and Moderna did not respond to repeated requests for comment.

In an internal email sent last July, Moderna notified its team of its latest efforts to shape the vaccine debate. “We have partnered with PGP (The Public Good Projects) and Moderna’s Global Intelligence, Corporate Security, Medical Affairs, Corporate Communications, Clinical Safety and Pharmacovigilance teams to provide media monitoring for misinformation at scale,” Marcy Rudowitz, the company’s customer program lead, wrote. “If and when a response is needed, our team will notify the appropriate stakeholders with recommendations,” she added.

The extent to which the company may intervene to shape content decisions is not clear. PGP continues to boast close relations with establishment institutions, including major medical associations.

The rise of censorship is inextricably connected to the pandemic, which emerged in the United States in early 2020. As federal, state, and local governments imposed unprecedented regulations on Americans in the name of public health, efforts arose to discredit counter-narratives that could be spread easily on social media. Early in the pandemic, criticism of policies such as lockdowns and vaccine mandates came almost entirely from independent media, which faced shadowbans and outright censorship on various platforms.

When they introduced their vaccines in 2021, manufacturers such as Moderna, Pfizer, and Johnson & Johnson also had a powerful financial interest in bolstering such censorship.

Moderna, perhaps more than other drug firms, is overwhelmingly reliant on the continued success of its vaccine. The company announced a price hike of up to $130 a dose this month, far higher than the $15–26 for American federal contracts, according to the Wall Street Journal. “We’re expecting a 90 percent reduction in demand,” Modena CEO Stéphane Bancel said, when he was asked to defend the decision. “As you can see, we’re losing economies of scale.”

Far from acting as a neutral arbiter, the Moderna Reports show that the company blurred the lines between public relations and public health. In many cases, Moderna’s intelligence and communications team targeted accurate information that had “the potential to fuel vaccine hesitancy” as menacing forms of misinformation in its reports. Given the size and scope and the censorship industrial complex, it can be difficult to draw a clear straight line between Moderna’s surveillance and actions taken against specific articles, posts, and writers. Instead, as Garay suggested, the company is one stream in an evolving ecosystem aimed at undermining dissent.

Alex Berenson

Independent journalist Alex Berenson is a repeated subject of the company’s surveillance efforts. A former reporter for the New York Times, Berenson quickly emerged as one of the most outspoken critics of vaccine-related policies. He was among the earliest to cast doubt on the Biden administration’s false claim that the vaccinated people could not transmit the COVID-19 virus to others. After government pressure on Twitter, Berenson was banned from the platform in 2021, only to return after successfully litigating against the company.

He appears to still be in the crosshairs. In September 2023, Moderna flagged a tweet from Berenson that highlighted the CDC’s data showing that among 1 million mRNA-vaccinated teenagers, there were from zero to a single COVID death and up to 200,000 side effects.

The company cited Berenson’s tweet under a report headline “Attacks on pediatric COVID-19 vaccines escalate” and claimed he had “cherry-picked data.” However, the company did not directly rebut any of Berenson’s claims in its report. Rather, Moderna noted the “high-risk” danger of Berenson’s viral tweet related to the potential for low child COVID-19 vaccination rates. “Fears about side effects and long-term dangers are major reasons parents report not vaccinating their children,” the report stated. It further concluded that “resistance to COVID-19 vaccines for children can be a gateway to broader anti-vaccine beliefs.”

Other Moderna reports flag Berenson’s tweets for “misinformation about mRNA safety” and claim that he is a “conspiracy theorist” for suggesting that health authorities have not properly taken into account the documented risks of myocarditis (inflammation of the heart muscle) for young men receiving the vaccine. Such questions have been posed by an increasing number of health professionals, but the misinformation reports dismiss any Berenson criticism as inherently false.

“It’s nice to know Moderna is watching me,” said Berenson, when asked about his response to the revelations. “I’m watching them too. mRNA shots carry unacceptably high heart risks for teenagers and young adults. Nearly the entire rest of the world accepts this reality and now discourages or bans people under 50 from taking mRNA Covid boosters. It is unconscionable that Moderna and Pfizer continue to market them to non-elderly adults.”

“They can call me whatever they like,” he noted, “but they can’t stop my reporting.”

Russell Brand

Russell Brand, the British commentator and comedian, is also a repeated name in the Moderna misinformation files. The left-leaning populist routinely pillories the pharmaceutical industry for exploiting the pandemic to generate unprecedented profits.
Moderna has closely monitored Brand’s criticism of the drug industry.

In various “low-risk” reports produced in August 2023, Moderna flagged videos produced by Brand twice. In one, Moderna noted that Brand had broadcast a monologue about Jonathan Van-Tam, a former senior health official who helped formulate COVID-19 policies in Britain. Van-Tam had just taken a position with Moderna, a move that raised eyebrows with many in the press. In the video, Brand noted that the company had just “made a fortune during the pandemic selling vaccines to the government,” and that the “government worker that bought all those vaccines” was now moving through the revolving door.

In another report, Moderna alleged that Brand “claimed that COVID-19 vaccine mandates were based on a lie in a recent podcast episode.” The video was broadly accurate. The monologue highlights CDC documents that had come to light showing that officials were aware that the virus would “break through” and still infect vaccinated patients. In an ironic twist, Brand finished the segment with a discussion of efforts to censor debate around the vaccine.

Moderna noted they were not yet taking action on this broadcast, but “we are monitoring with our partner, the Public Good Projects.”

The following month, several media outlets reported that several women who insisted on anonymity were claiming that Brand had abused them nearly twenty years ago. The ensuing media firestorm, which led to YouTube demonetizing his account, became fodder for other Moderna misinformation reports. The company warned that the cancellation of Brand was sparking a backlash among social media users, who believed that he may be targeted by government and corporate censors for his outspoken opposition to pandemic narratives.

In a Moderna high-risk report, the company noted that speculation was swirling that “allegations are part of a conspiracy to silence the comedian, who has been a vocal opponent of COVID-19 vaccines.” The report linked an X video of Brand sharply criticizing Moderna and Pfizer for generating “$1,000 of profit every second” in 2021. The specific claim of profiteering was a mainstream claim, a statistic that was produced by Oxfam.

Nowhere in its reports on Brand did Moderna highlight any incorrect information. But the reports noted that they monitored Brand because he “has a large platform with over 6.6 million YouTube subscribers and over 21 million followers across multiple social media platforms.” Moreover, his “videos are widely circulated in anti-vaccine spaces where he is viewed as a truth-teller and threat to authority,” and that Brand maintained support from Tucker Carlson and Elon Musk.

Michael Shellenberger

The Moderna misinformation reporting system reveals that the pharmaceutical firm maintained an interest in pandemic-related issues that go beyond vaccine policy, overlapping with general issues surrounding the unexplained questions that still swirl around the source of the pandemic.

The company, for instance, flagged discussions around news last year of a congressional whistleblower who came forward with allegations that the CIA suppressed an assessment from analysts that COVID-19 originated at the Wuhan Institute of Virology. The story has garnered widespread coverage in NBC, Science, and ABC News, among other outlets.

But Moderna’s misinformation alerts flagged Sen. Rand Paul (R-Ky.) and journalist Michael Shellenberger for distributing information about the CIA allegation. Shellenberger—with whom this reporter has worked on the Twitter Files—had exclusively reported earlier last year that U.S. government sources believed that the “patient zeros” of COVID-19 were a group of Chinese scientists at the Wuhan lab—a major revelation later confirmed by the Wall Street Journal.

Despite his work on the issue, Moderna dismisses Shellenberger in its reports as among its known “misinformation authors.”

“Moderna has spent years spreading disinformation about their vaccines and so it makes sense that they would smear the scientists and journalists who expose them as conspiracy theorists and sources of misinformation,” Shellenberger told RCI.

“The question is why is Moderna spreading disinformation on the high probability that Covid escaped from the Wuhan Institute of Virology lab?” he added. “A company that makes its money selling a coronavirus vaccine shouldn’t care where Covid came from.”

More here:

https://www.theepochtimes.com/opinion/how-moderna-came-up-with-a-vaccine-against-vaccine-dissent-5567090?ea_src=au-frontpage&ea_med=opinion-5

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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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DNA Contaminants in COVID Vaccines Are ‘Beyond the Pale’: Florida Surgeon General Explains the Call for Vaccine Halt

On Jan. 3, the office of Florida Surgeon General Dr. Joseph Ladapo issued a statement calling for the halt in the use of COVID-19 mRNA vaccines, citing the recent discovery of DNA contaminants in the vaccine vials.

On the Jan. 12 episode of EpochTV’s “American Thought Leaders,“ Dr. Ladapo explained why he called for a halt, saying that while there are also safety concerns with the COVID mRNA vaccines linking them to a multitude of adverse events, the recent discovery is ”beyond the pale.”
“DNA is a common contaminant of many biological products,” he told the show’s host, Jan Jekielek. “We can use DNA to produce different drugs like insulin, other biologics—and that’s a wonderful innovation, and normally, that DNA doesn’t pose a problem.”

Human cells are resistant to DNA entry, and this prevents harming the integrity of the cell’s DNA.

However, since the mRNA vaccines use lipid nanoparticles, which deliver mRNA into the cells directly, DNA contaminants could also be able to enter the cells. Some scientists, like Dr. Ladapo, are concerned that the DNA from the vaccine may integrate with the human genome.

Prominent officials at the U.S. Food and Drug Administration (FDA) disagree.

On Dec. 6, Dr. Ladapo sent a letter to FDA commissioner Dr. Robert Califf and the U.S. Centers for Disease Control and Prevention (CDC) director, Dr. Mandy Cohen. In his letter, he asked if there have been risk assessments of the vaccine DNA integrating into human DNA, especially regarding the controversial SV40 promoter/enhancer region found in Pfizer’s vaccine.

Other questions included whether risk assessments have been done on DNA integration in reproductive cells and if the current levels of DNA residuals are acceptable under the FDA’s standards.

“We’ve gotten ... lengthy responses that don’t answer the question,” Dr. Ladapo said.

In his response, Dr. Marks wrote that DNA integration “is quite implausible,” adding that animal studies show “no evidence indicative for genotoxicity.”
No tests were mentioned that would assess if DNA integration is occurring.

Dr. Ladapo believes it would be reckless not to test for DNA integration, a potential risk once DNA enters the cell.

“Their position is, oh, no, it’s fine. Everything’s fine; safe and effective. That’s not only not good enough, but it’s completely unacceptable,” Dr. Ladapo said. “And that’s why I made that determination, and it’s absolutely the correct call.”

DNA Contamination: The SV40 Promoter Controversy

Both Moderna and Pfizer mRNA vaccines contain DNA contaminants, but only the Pfizer vaccines have also been found to contain SV40 promoter/enhancer DNA, which has since become a topic of debate.
SV40, or simian vacuolating virus 40, is a DNA virus that sometimes causes cancer in animals.

However, the SV40 promoter/enhancer found in the vaccines is only a tiny section of the DNA; it is not equivalent to the entire SV40 virus or its protein.

Promoter-enhancers are sections of DNA that can control the activity of other DNA.

“With DNA, there are different regions that tell other parts of DNA whether to be active or not,” Dr. Ladapo said. “This type of control process is very important ... The absence of control can, for example, lead to cancer ... [and] other metabolic abnormalities.”

In his letter to the FDA, Dr. Ladapo asked about the additional risk of the SV40 promoter/enhancer region’s DNA integration.

Dr. Marks answered that there were no genes for SV40 proteins nor SV40 proteins themselves present in the vaccine.

But Dr. Ladapo believes Dr. Marks is intentionally not answering the question. “No one’s talking about SV40 protein ... we talked about the promoter/enhancer region. They have to be doing it intentionally,” Dr. Ladapo said.

The Risks of DNA Integration

It is currently unknown whether DNA introduced into the body is being integrated into the cell’s human genome; and if it’s integrated, what impact will it have.

Only around 1 percent of the human DNA produces protein; the job of the other 99 percent of DNA is mostly unknown.

“There’s ... a lot of uncertainty about our genome—what it does, how it supports life and creates life, and creates the miracle of each individual human being,” Dr. Ladapo said. “What we do understand is that some of the potential risks of DNA integration include development of cancers, because ... of the regulation of different aspects of DNA and cell growth.

“Other possibilities include the disruption of the normal expression of some proteins, which then subsequently could lead to disruption of normal human function.”

Since biodistribution studies in rats have shown that the mRNA vaccines can accumulate in the reproductive organs, Dr. Ladapo’s letter expressed concern that there may also be DNA integration of reproductive cells.

“We are the most complex beings—the most complex machines, if you will—living machines that exist on this Earth. So I do believe that our genome is part of our connection to God. So that is to say that there’s quite a lot at risk in terms of not taking proper precautions and sensible precautions, with maintaining the integrity to the best that we can—life ain’t perfect, but to the best that we can with our human genome.”

https://www.theepochtimes.com/health/dna-contaminants-in-covid-vaccines-are-beyond-the-pale-florida-surgeon-general-explains-the-call-for-vaccine-halt-5566113?ea_src=ai_recommender&ea_med=desktop_health

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FDA Launches Fresh Bid to Toss Out High-Profile Ivermectin Case

The U.S. Food and Drug Administration (FDA) is seeking to persuade a federal court to dismiss a lawsuit challenging its repeated advisories against using ivermectin to treat COVID-19.

The FDA in a sealed motion asked the U.S. District Court for the Southern District of Texas to dismiss the suit, which was brought by three doctors who allege the FDA’s warnings were illegal.

The late 2023 motion was sealed because exhibits the government cited “include confidential information” from a separate legal proceeding, according to a government brief.

Government lawyers said they would file redacted versions of the motion for public perusal but still haven’t done so.

Attorneys for the doctors said on Jan. 12 that the court should reject the government’s fresh bid to throw out the case.
“The FDA exceeded its authority by repeatedly issuing public directives not to use ivermectin for COVID-19, even though the drug remains fully approved for human use,” they wrote.

The government motion came after an appeals court found that the FDA likely overstepped its authority with the warnings.
“FDA can inform, but it has identified no authority allowing it to recommend consumers ’stop' taking medicine,” U.S. Circuit Judge Don Willett, an appointee of then-President Donald Trump, wrote in the ruling.

The appeals court remanded the case back to U.S. District Judge Jeffrey Brown, who said in 2022 that the doctors failed to prove their allegations.
The FDA in the sealed motion asked Judge Brown, another appointee of President Trump, to dismiss the case.

According to lawyers for the doctors, the FDA’s motion includes the argument that the plaintiffs haven’t suffered injuries that are traceable to the FDA and that can’t be remedied by a ruling in favor of the plaintiffs.

“The FDA is wrong,” the lawyers said. “Plaintiffs have suffered interference with their practice of medicine and the doctor-patient relationship, economic harm, reputational harm, and increased exposure to malpractice liability, and have been subject to disciplinary proceedings and forced resignations, all of which clearly trace to the FDA’s campaign against ivermectin and would be remedied by equitable relief.”

The Federal Food, Drug, and Cosmetic Act enables the FDA to authorize or approve drugs for a specific use, but doctors are free to prescribe cleared drugs for other purposes, in what’s known as “off-label” prescribing. The law doesn’t grant authority to the FDA to regulate off-label use.

The plaintiffs include Dr. Robert Apter, who was investigated by medical boards in two states for prescribing ivermectin to treat COVID-19. The referrals to the boards include some of the FDA’s warnings against using the drug as a COVID-19 treatment.

The FDA’s position in seeking a dismissal stems in part from the negative actions against the plaintiffs being taken by third parties such as pharmacies, according to a description of the sealed motion. It was quoted as saying that the referrals “are not fairly traceable” to the FDA’s statements.

An exhibit included by the FDA, however, showed that one of the referrals came from a pharmacist who cited FDA documents as a reason for “increased scrutiny” with regard to ivermectin prescriptions. The pharmacist wrote that Dr. Apter wouldn’t provide a “valid medical reason” for the ivermectin prescription and was thus engaging in “inappropriate prescribing.”

“The FDA is the common thread through all of [the] plaintiffs’ injuries, which began only after the FDA embarked on its campaign to stop the use of ivermectin for COVID-19 and which often involve explicit invocation of the FDA’s directives and recommendations,” the plaintiffs’ lawyers said.

They are seeking an order that would force the FDA to rescind or amend its warnings. That would remove the justification of the parties that have taken actions against the plaintiffs, the lawyers added.

https://www.theepochtimes.com/health/fda-launches-fresh-bid-to-toss-out-high-profile-ivermectin-case-5566009

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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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