Vaccine Deaths; Crimes Against Humanity; Game-changer for Autism; FDA Withholding Autopsy Results on People Who Died After Getting COVID-19 Vaccines

‘Game-changer for autism’: 100-year-old drug reverses symptoms, study finds

  A drug discovered more than 100 years ago may hold the key to combating autism symptoms, according to a study.

Researcher Dr Robert Naviaux of the San Diego School of Medicine gave suramin, a drug first developed in 1916, to 10 autistic boys between the ages of five and 14, and noted transformative results.

“After the single dose, it was almost like a roadblock had been released,” he said“If the future studies show that there’s continued health benefits, this could be a game-changer for families with autism.”

The study, which has been published in the Annals of Clinical and Translational Neurology, saw five of the participants receive suramin, while the remainder were given placebos. Included in the group were four non-verbal children – two six year olds and two 14 year olds.

“The six year old and the 14 year old who received suramin said the first sentences of their lives about one week after the single suramin infusion,” Naviaux told the UC San Diego Health website“This did not happen in any of the children given the placebo.”

Research has shown that cells harden their membranes in response to attacks from viruses or pollutants. The reaction, known as ‘cellular danger response’ (CDR), is a common defense mechanism that allows cells to wait for danger to pass. Autism is thought to develop during early childhood when cells can become ‘stuck’ in this mode.

One parent, whose son had not spoken a full sentence in more than a decade, said: “Within an hour after the infusion, he started to make more eye contact with the doctor and nurses in the room. There was a new calmness at times, but also more emotion at other times.” 

“He started to show an interest in playing hide-and-seek with his 16-year-old brother. He started practicing making new sounds around the house. He started seeking out his dad more.”

First tested on mice in 2013, this is the first time suramin has been administered to children.

For Naviaux, the challenge now is to widen his research to a bigger sample testing size. “This work is new and this type of clinical trial is expensive,” he said. “We did not have enough funding to do a larger study. And even with the funding we were able to raise, we had to go $500,000 in debt to complete the trial.”  https://www.rt.com/usa/390222-autism-research-suramin-symptoms/

EXCLUSIVE: FDA Withholding Autopsy Results on People Who Died After Getting COVID-19 Vaccines

By Zachary Stieber
September 29, 2022 Updated: September 29, 2022
The U.S. Food and Drug Administration (FDA) is refusing to release the results of autopsies conducted on people who died after getting COVID-19 vaccines.

The FDA says it is barred from releasing medical files, but a drug safety advocate says that it could release the autopsies with personal information redacted.

The refusal was issued to The Epoch Times, which submitted a Freedom of Information Act for all autopsy reported obtained by the FDA concerning any deaths reported to the Vaccine Adverse Event Reporting System following COVID-19 vaccination.

Reports are lodged with the system when a person experiences an adverse event, or a health issue, after receiving a vaccine. The FDA and other agencies are tasked with investigating the reports. Authorities request and review medical records to vet the reports, including autopsies.

The FDA declined to release any reports, even redacted copies.

The FDA cited federal law, which enables agencies to withhold information if the agency “reasonably foresees that disclosure would harm an interest protected by an exemption,” with the exemption being “personnel and medical files and similar files the disclosure of which would constitute a clearly unwarranted invasion of personal privacy.”

Federal regulations also bar the release of “personnel, medical and similar files the disclosure of which constitutes a clearly unwarranted invasion of personal privacy.”

The Epoch Times has appealed the denial, in addition to the recent denial of results of data analysis of VAERS reports.

‘Easily Be Redacted’

Kim Witczak, a drug safety advocate who advises the FDA as part of the Psychopharmacologic Drugs Advisory Committee, said that the reports could be released with personal information blacked out.

“The personal information could easily be redacted without losing the potential learnings from [the] autopsy,” Witczak told The Epoch Times via email.

People make the choice to submit autopsy results to the Vaccine Adverse Event Reporting System, Witczak noted.

“If someone submits their experience to VAERS they want and expect to have it investigated by the FDA. This includes autopsy reports,” she said.

Autopsies are examinations of deceased persons performed to determine the cause of death.

“Autopsies can be an important part of postmortem analysis and should be done especially with increased deaths following COVID-19 vaccination,” Witczak said.

FDA Responds

An FDA spokesperson noted that deaths following COVID-19 vaccination are rare, citing the number of reports made to VAERS.

As of Sept. 14, 16,516 reports of death following COVID-19 vaccination have been reported. Approximately 616 million doses have been administered in the United States through September.

The spokesperson declined to say whether the FDA would ever release the autopsy results, but pointed to a paper authored by researchers with the FDA and the Centers for Disease Control and Prevention (CDC).

The paper, which has not been peer reviewed, analyzed the approximately 9,800 reports of death to VAERS following COVID-19 vaccination lodged from Dec. 14, 2020, to Nov. 17, 2021. Researchers found that reporting rates were lower than the expected all-cause mortality rates.

“Trends in reporting rates reflected known trends in background mortality rates. These findings do not suggest an association between vaccination and overall increased mortality,” the researchers wrote.

The researchers noted that prior studies have found that adverse events reported to VAERS are an undercount of the true number of events.

Zachary Stieber

REPORTER

 

Attorney Tom Renz Discusses Truth For Justice

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Doctor Blasts White House’s Annual COVID-19 Vaccination Plan

‘The biggest mistake we’ve made ever made in the history of medicine’
By Steve Lance and Naveen Athrappully
September 12, 2022

The Biden administration’s plan to make COVID-19 shots an annual event has come under criticism from some experts, including a medical doctor in Oklahoma who said the move will serve corporate interests.

In a statement released Sept. 8, the White House revealed its plan to get more Americans injected with an updated COVID-19 vaccine.

“As the virus continues to change, we will now be able to update our vaccines annually to target the dominant variant,” the statement said. The Biden administration has secured more than 170 million doses of the updated vaccines to be distributed to Americans.

Dr. Jim Meehan, who operates a functional medicine practice, said the push to continue vaccinating people with COVID-19 shots and boosters is not based in science or medicine.

“This is not the scientific process. This, in my opinion, this is corporatocracy. This is the FDA being captured by the pharmaceutical industry,” Meehan said in a recent interview for NTD’s “Capitol Report” program.

Meehan said it’s not surprising that the pharmaceutical companies are trying to turn COVID-19 shots into a revenue stream.

Individuals at the Food and Drug Administration (FDA) who pushed for making pharmaceutical companies commit to more experiments and safety trials on the COVID-19 vaccines have been removed from the agency, Meehan says. Two leaders of the FDA’s vaccine division resigned after being frustrated due to being pressured by the Biden administration.

The updated vaccine has only been tested in eight mice, Meehan pointed out, and the tests were only conducted to see if the vaccine produced more antibodies.

“Antibody elevation does not equate to protection,” he said.

An annual vaccine “isn’t going to help anybody except the pharmaceutical company,” Meehan said, since the efficacy of these shots lasts only three to four months at best. Moreover, the antibodies seem to be “enhancing” the coronavirus.

More Deaths

After going through more than 11,000 vaccine adverse event reports, Meehan found that there were over 30,000 reports of death in a database set up by Congress to monitor the safety signals of vaccines.

He believes the database is underreporting by a factor of 41, which would put COVID-19 vaccine-related deaths of Americans at about 1.2 million.

Pharmaceutical companies have no liability in such events, and no one is held accountable, Meehan said.

“Historically, this is the biggest mistake we’ve ever made in the history of medicine, science, the scientific method,” he said.

Some people who have taken COVID-19 vaccines are experiencing heart inflammation, Meehan stated. Young athletes are being compelled to get vaccinated by their athletic organizations.

People who have statistically zero risk of dying from the virus are being coerced into taking a shot and are paying a terrible price, he said.

Studies published in journals such as the Journal of the American Medical Association show that young men who receive a COVID-19 vaccine are at 133 times greater risk of myocarditis (inflammation of the heart) from the injection than from the virus itself, Meehan said.

No adequate safety tests have been conducted on the vaccine, and low-level observational studies funded by pharmaceutical companies like Pfizer Inc. and Moderna Inc. are being used instead, which in itself represents a conflict of interest, Meehan stated.

“We’re getting pseudoscience to support a false narrative for a vaccine that has failed and we’re just continuing to push it in more and more arms. I don’t know what’s driving that,” he said. “I really don’t know what level of incompetence, ignorance, or perhaps malevolence is driving it, but it’s got to stop.”

Steve Lance

Naveen Athrappully is a news reporter covering business and world events at The Epoch Times.

FDA Refuses to Provide Key COVID-19 Vaccine Safety Analyses; More COVID Vaccine Linked Heart Inflammation

EXCLUSIVE: FDA Refuses to Provide Key COVID-19 Vaccine Safety Analyses

By Zachary Stieber
September 10, 2022 Updated: September 11, 2022

U.S. drug regulators are refusing to provide key analyses of a COVID-19 vaccine safety database, claiming that the factual findings cannot be separated by internal discussions protected by law.

The Epoch Times asked the Food and Drug Administration (FDA) in July for all analyses performed by the agency for the COVID-19 vaccines using a method called Empirical Bayesian data mining, which involves comparing the adverse events recorded after a specific COVID-19 vaccine with those recorded after vaccination with non-COVID-19 vaccines.

According to operating procedures laid out by the agency and its partner in January 2021 and February 2022, the FDA would perform data mining “at least biweekly” to identify adverse events “reported more frequently than expected following vaccination with COVID-19 vaccines.” The agency would perform the mining on data from the Vaccine Adverse Event Reporting System (VAERS).

In a recent response, the FDA records office told The Epoch Times that it would not provide any of the analyses, even in redacted form.

The agency cited an exemption to the Freedom of Information Act that lets the government withhold inter-agency and intra-agency memorandums and letters “that would not be available by law to a party other than an agency in litigation with the agency.”

The agency also pointed to the Code of Federal Regulations, which says that “all communications within the Executive Branch of the Federal government which are in written form or which are subsequently reduced to writing may be withheld from public disclosure except that factual information which is reasonably segregable in accordance with the rule established in § 20.22 is available for public disclosure.”

It’s not clear why the FDA could not produce copies of the analyses with non-factual information redacted. The Epoch Times has appealed the determination by the records office. The FDA declined to comment, citing the appeal.

‘Unacceptable’

Kim Witczak, co-founder of Woodymatters, a nonprofit that advocates for a stronger FDA and drug safety system, said the agency’s refusal to provide the analyses was not acceptable.

“The secrecy is unacceptable for an agency that said it is transparent with the public about vaccine safety,” Witczak, who sits on one of the FDA’s outside advisory panels, told The Epoch Times.

“What’s the point of having VAERS if you’re not releasing it to the public?” she added.

Witczak said her concerns about vaccine safety were heightened by a recent paper from Dr. Joseph Fraiman and others that found a higher incidence of serious adverse events in vaccinated participants in the original Pfizer and Moderna vaccine trials than in placebo recipients. She noted that the FDA’s 2004 warning for antidepressants that the drugs could increase the risk of suicidal thoughts and behavior came over 10 years after the trials on which it was based.

“If this data is available, shame on you for not making it known to the public,” Witczak said. “It’s as if they don’t trust the people to make their own best decision for what’s good for them and their families.”

Epoch Times Photo
A healthcare worker prepares a COVID-19 vaccine in Southfield, Mich., in an Aug. 24, 2021, file image. (Emily Elconin/Getty Images)

CDC

The Centers for Disease Control and Prevention (CDC), according to the documents outlining operating procedures, was going to perform a different type of data mining analyses, called Proportional Reporting Ratio (PRR) mining.

The CDC has also refused, so far, to provide the results for those analyses.

It has also twice provided false information when responding to questions.

The agency initially said that no PRR analyses were done and that data mining is “outside of th[e] agency’s purview.” The agency then said that it did perform PRRs, starting in February 2021.

Later, the agency acknowledged that wasn’t true. The agency did not begin performing PRRs until March 2022, a spokesperson told The Epoch Times.

Roger Andoh, a records officer, gave the initial response, citing the CDC’s Immunization and Safety Office. Dr. John Su, a CDC official, gave the second response. It remains unclear with whom the information originated.

The Epoch Times has submitted Freedom of Information Act requests for internal emails that may provide answers.

Data Mining Reports

The Empirical Bayesian (EB) is focused on identifying disproportional numbers of adverse events, CDC scientist Dr. Tom Shimabukuro said in January 2021. It identifies “with a high degree of confidence, adverse event-vaccine pairs reported at least twice as frequently as expected for a COVID-19 vaccine compared to the VAERS database,” he said, or a comparison between the incidence of a specific event such as kidney disease after COVID-19 vaccine compared to the incidence of the same event after all other U.S.-licensed vaccines.

The FDA and CDC have provided periodic updates on the EB data mining effort.

“Importantly, there were no Empirical Bayesian data mining alerts detected for any adverse event COVID-19 vaccine pairs as of the last data mining run that the FDA performed on February 18th,” Shimabukuro told members of the FDA’s vaccine advisory panel on Feb. 26, 2021.

In a review memorandum (pdf) for an expansion of the emergency authorization granted to Pfizer’s vaccine, FDA researchers said that data through April 16, 2021, showed only a possible signal for body temperature.

In the journal Vaccine in June 2021, FDA researchers said an analysis of cases of blood clotting after the Pfizer and Moderna vaccines did not suggest a safety concern. The FDA and CDC paused the Johnson & Johnson vaccine in April 2021 over cases of blood clotting, some fatal, but lifted the pause just 10 days afterward. The FDA later restricted use of the Johnson & Johnson shot.

In a paper in the CDC’s quasi-journal in August 2021, FDA and CDC researchers said that the FDA used EB mining to monitor events in children aged 12 to 17 after vaccination. The results indicated a lack of a safety signal for post-vaccination heart inflammation, or myocarditis, though other surveillance systems had detected the issue as an adverse event.

In a preprint study in October 2021 later published in The Lancet, government scientists said no adverse health outcomes were identified with the EB mining.

And in a preprint in May 2022, scientists, including Su, said that EB mining analyzing data through Nov. 12, 2021, revealed only one signal for VAERS death reports, for “vaccination failure” after receipt of the AstraZeneca vaccine, which is not authorized in the United States.

Zachary Stieber

REPORTER

More Reports of COVID Vaccine-Linked Heart Inflammation in Young Males Submitted to CDC

By Jack Phillips  September 11, 2022 Updated: September 11, 2022

 

Reports submitted to the U.S. Centers for Disease Control and Prevention (CDC)’s vaccine surveillance system suggest that cases of post-COVID-19 vaccine-linked heart inflammation among young males have risen.

Recent figures published in the CDC’s Vaccine Safety Datalink surveillance system show that within a week of getting the two-dose Pfizer-BioNTech vaccine, there were 14 cases of myocarditis or pericarditis among 102,091 males between the ages of 16 and 17. And of the 206,000 12- to 15-year-old males who got the same two-dose vaccine series, there were 31 cases within a week, according to the CDC (pdf).

Those reports were presented to the CDC’s Advisory Committee on Immunization Practices on Sept. 1 show that the incident rate for the 12- to 15-year-old group is 150.5 per million—or about 1 in 6,600—and 137.1 per million for the 16- to the 17-year-old group—or about 1 in 7,262.

Following the first booster dose, CDC-presented figures show that it jumps to 188 per million among the 16- to 17-year-old group. But for the 12- to 15-year-old males, 61.3 per million developed heart inflammation after the booster dose, according to the figures.

In August 2021, the figures submitted to the CDC system (pdf) show that of 42.6 myocarditis and pericarditis cases per million and 71.5 per million for 12- to 15-year-old males and 16- to 17-year-old males, respectively. That breaks down to about one in 23,500 for the younger group and around one in 14,000 for the older group.

Epoch Times Photo
The CDC’s Sept. 1, 2022, data shows instances of myocarditis and pericarditis among children and younger adults. (CDC.gov)

The agency noted that “myocarditis is a rare event following mRNA COVID-19 booster vaccination” and that it has “verified 131 myocarditis case reports to VAERS in people ages [5 years and older] after 123,362,627 million mRNA COVID-19 booster vaccinations.”

In analyses of the data, “myocarditis [and] pericarditis incidence following first booster dose and dose 2 of the primary series are similar, though case counts are small and confidence intervals around point estimates are wide,” said the CDC.

Epoch Times Photo
CDC data from August 2021 shows the instances of myocarditis and pericarditis among children and young adults. (CDC.gov)

The Vaccine Safety Datalink is described by the agency as “a collaborative project between CDC’s Immunization Safety Office and nine health care organizations” and is designed to “monitor [the] safety of vaccines and conduct studies about rare and serious adverse events following immunization.”

In May, the CDC said reports of heart inflammation linked to the Pfizer vaccine were much lower in 5- to 11-year-old boys than in adolescents and young males. Among that group, the rate of heart inflammation stood at 2.7 cases per million.

Another Study

After the figures were presented, the Advisory Committee on Immunization Practices recommended updated boosters, which was, in turn, endorsed by CDC Director Rochelle Walensky, the CDC’s director.

Walensky said that “updated COVID-19 boosters are formulated to better protect against the most recently circulating COVID-19 variant,” adding, “They can help restore protection that has waned since previous vaccination and were designed to provide broader protection against newer variants.”

“This recommendation followed a comprehensive scientific evaluation and robust scientific discussion. If you are eligible, there is no bad time to get your COVID-19 booster and I strongly encourage you to receive it,” she added on Sept. 1.

A study that was led by Dr. Tracy Hoeg, with the Florida Department of Health, and released in mid-2021 showed figures similar to the ones submitted to the CDC’s advisory committee on Sept. 1.

Hoeg said she and others published a preprint study last year showing a rate of 94 instances of myocarditis per million in 16- to 17-year-old males—or 1 in 10,6000—and 162 per one million in 12- to 15-year-old males—or 1 in 6,200—she wrote on Sept. 1.

The CDC “is now finally catching up & reporting similar,” Hoeg wrote on Twitter earlier this month.

“If we hadn’t been villified as ‘anti-vaxxers’ spreading ‘mis’ & ‘disinformation,’ how would the conversation around minimizing the chance of this adverse event have changed & how many cases of myo/pericarditis in young males would have been prevented over the last year?” she asked.

Hoeg also questioned recent statements made by CDC officials in recommending boosters to anyone aged 12 and older.

“Now today the CDC is recommending with no human data on benefits or risks that everyone 12 and up get a bivalent booster. ‘There is no bad time to get your COVID-19 booster.’ Really?” she asked. “Why are nuance & individualized recs so difficult for @CDCgov?”

Mortality in the 25 to 34 age group up 78 Percent; Israel Found and Covered Up Serious Side Effects; ‘Irrefutable Proof’ That mRNA Vaccines Cause Vascular and Organ Damage

A former Wall Street analyst and BlackRock portfolio manager, Edward Dowd has been analyzing excess mortality data from the CDC (https://www.theepochtimes.com/t-cdc) and from insurance companies with his partner, Josh Stirling, an insurance analyst. Excess mortality or excess deaths (https://www.theepochtimes.com/t-excess-deaths) refers to the number of deaths from all causes above what would be expected under normal circumstances.

Earlier this year, the CEO of a major life insurance company said death rates among working-age Americans had gone up 40 percent from pre-pandemic levels. A recent report by the Society of Actuaries now reinforces this alarming data, Dowd says.

‘In the 25 to 34 [age group], they saw 78 percent excess mortality in the third quarter of 2021. They also saw, in the 35 to 44 age group, 100 percent excess mortality,’ Dowd says.”


13 Minutes of Never-Before-Seen Footage of Ballot Trafficking in Detroit, Michigan

“Election Integrity investigators in Detroit, Michigan captured never-before-seen footage of DOZENS of ballot traffickers dumping HUNDREDS of ballots into ballot drop boxes during the 2020 US presidential election.

The exclusive drop-box footage from the 2020 presidential election was obtained by The Gateway Pundit and Attorney John Burns.

The MC4EI team in Michigan spent hours scouring through the thousands of hours of security camera footage to put together this explosive 13-minute-video.

Special thanks to Patty McMurray and 100 Percent Fed Up for her help in coordinating this effort.

Israel Found and Covered Up Serious Side Effects From Pfizer COVID Vaccine

Israel didn’t start to gather safety data until a year into the vaccine program. They gathered 6 months worth of data and found that the vaccines weren’t safe so they lied to the world about it.


Dr. Peter McCullough: “In France, they took hydroxychloroquine off the over-the-counter market months before the virus was even announced.”

“The suppression of early treatment and the suppression of any advancement in hospital care was intentional to create fear, suffering, hospitalization, and death in order to prepare the world’s population to accept mass vaccination — with no end in sight.”


‘Irrefutable Proof’ That mRNA Vaccines Cause Vascular and Organ Damage: Study

By Enrico Trigoso
September 9, 2022 Updated: September 10, 2022

A recent study claims to have found “irrefutable proof of causality” that the mRNA vaccines cause vascular and organ damage.

The study, conducted by microbiologists Dr. Michael Palmer and Dr. Sucharit Bhakdi, was mostly based on the findings of German pathologists Dr. Arne Burkhardt and Dr. Walter Lang.

Here is a summary of the findings:

  1. mRNA vaccines don’t stay at the injection site; they instead travel throughout the body and accumulate in various organs.
  2. mRNA-based COVID vaccines induce long-lasting expression of the SARS-CoV-2 spike protein in many organs.
  3. Vaccine-induced expression of the spike protein induces autoimmune-like inflammation.
  4. Vaccine-induced inflammation can cause grave organ damage, especially in vessels, sometimes with deadly outcomes.

“This study, by the type of dyes they use, shows irrefutable proof that the spike protein goes everywhere—heart, ovary, liver, spleen—and to a lesser extent, testes.” Dr. Sherri Tenpenny, an expert in vaccine damage, told The Epoch Times.

“This is what leads to multi-organ system failure. This is what leads to infertility in women.”

“There has been a lot of hypothesis about the damage these shots cause. Now, with these pathology slides and the specific types of immunochemistry staining, Bhakti and Palmer show—unequivocally—that the spike protein is quickly disseminated to every organ they examined,” Tenpenny said.

“They are both pathologists; looking at slides of tissue under a microscope and appropriately staining tissue is what they are trained to do!” she added.

“Those of us who warned of the dangers of these COVID shots were widely censored and ridiculed,” Dr. Christiane Northrup, former fellow in the American College of Obstetricians and Gynecologists, told The Epoch Times.

“I wish we had been wrong. We weren’t. And we finally have irrefutable proof,” Northrup added.

According to toxicologist Janci Lindsay, Ph.D., who has been following the COVID vaccine story since its inception, the most valuable takeaway from this study is that it “corroborates” Markus Aldén et al.’s findings (in-vitro) that Pfizer’s COVID-19 vaccine may be transcribed into cellular DNA—in an in-vivo system.

In-vitro, which means “in glass” in Latin, refers to when a test or process is done in a test tube or outside a living organism. In-vivo (within the living) means the studies are done in living organisms.

That the vaccine quickly distributes through the body was a finding present in Pfizer’s own animal experiments.

“The subject was deceased but the examination of their tissue showed that they were expressing the spike protein, nine months after the injection of the genetic vaccine,” Lindsay told The Epoch Times.

The only three possible ways that the abovementioned could happen, she explains, are when:

  1. mod-mRNA is stable in the body for nine months.
  2. The mRNA has been integrated into the genome, such as in the Aldén study.
  3. The person was around somebody who was recently vaccinated and the mRNA was transmitted.

The Palmer and Bhakdi study says that the “limited experimental studies available (20152018)” indicate that the injected modified mRNA should degrade “within days to a few weeks of the injection.”

But, “this is obviously difficult to square with the observed long-lasting expression; in some form or other, the genetic information appears to be perpetuated in-vivo,” the study states.

“Their findings of spike expression nine months out from [taking the vaccine] support either genomic integration of the mRNA coding the spike protein into the genome of the cells shown expressing it, or, that the synthetically modified messenger RNA is remaining stable within these cells months after it was supposed to be degraded,” Lindsay said.

“This constitutive expression of the spike protein would exhaust the immune system and/or eventually possibly make it non-responsive or tolerant to the spike protein, allowing for untold spike-mediated damage,” she added.

Method

The methods used by Dr. Burkhardt are called histopathology and immunohistochemistry.

The technique is explained in the study: “If a vaccine particle—composed of the spike-encoding mRNA, coated with lipids—enters a body cell, this will cause the spike protein to be synthesized within the cell and then taken to the cell surface. There, it can be recognized by a spike-specific antibody.”

“After washing the tissue specimen to remove unbound antibody molecules, the bound ones can be detected with a secondary antibody that is coupled with some enzyme, often horseradish peroxidase,” it reads. “After another washing step, the specimen is incubated with a water-soluble precursor dye that is converted by the enzyme to an insoluble brown pigment. Each enzyme molecule can rapidly convert a large number of dye molecules, which greatly amplifies the signal.”

“Histo” comes from the Greek word for “web, tissue.”

Epoch Times Photo
Image 3: Expression of viral proteins can be detected with immunohistochemistry. (Michael Palmer, MD, Sucharit Bhakdi, MD)

“At the top right of the image, you can see two cells which were exposed to the Pfizer vaccine and then subjected to the protocol outlined above. The intense brown stain indicates that the cells were indeed producing the spike protein,” the study reads, referring to image 3.

Epoch Times Photo
Expression of spike protein in shoulder muscle after vaccine injection. (Michael Palmer, MD, Sucharit Bhakdi, MD)

Rebuttal

Health Feedback, a member of the Vaccine Safety Net led by the WHO, on Sept. 3 said that these claims are “unsubstantiated.”

“The idea that mRNA from COVID-19 vaccines can remain in our bodies in the long term is a common myth with no scientific basis,” the WHO fact-checking branch states.

“mRNA from vaccines is fragile and gets rapidly degraded by cellular machinery once it has delivered the genetic instructions. The spike protein generated by COVID-19 vaccines is thought to remain in the body for up to a few weeks, like other proteins made by the body,” they add.

Blood Vessel Inflammation

The second biggest discovery, Lindsay believes, would be the observation of endothelial damage—inflammation and denuded endothelial cells inside the blood vessels.

Endothelium is the tissue that lines the blood vessels and other organs, such as the heart.

“Spike protein disease is an endothelial disease—very key to myocarditis, etc.,” Dr. Tenpenny said.

Epoch Times Photo
Endothelial stripping and destruction of a small blood vessel after vaccination. (Michael Palmer, MD, Sucharit Bhakdi, MD)

Dr. Wade Hamilton, a cardiologist who has been punished by the medical establishment for giving an exemption to a COVID vaccine, commented on the study.

“The first 13 items in and of themselves are major reason for concern and halting the COVID shot use,” Hamilton told The Epoch Times.

“Item 14 (Aldén study), which concerns the possibility that the shot can alter the DNA of recipients and subsequently the DNA of their offspring, is of great concern,” Hamilton said.

“The paper I have sent (comment on Aldén et al.) raises unanswered questions, the three easiest to understand are:

  1. The dose of mRNA used in this study is higher than mRNA in the COVID shot.
  2. The Alden study is in-vitro (not in-vivo) and the normal human immune and chemical protections are not present.
  3. The liver cells used in the experiment are liver cancer cells and their response to reverse transcriptase may not be typical.

“It is possible as queried in the comment on Aldén et al. paper, that persistent pieces of DNA or mRNA in people with COVID lead to persistent circulating spike protein as a cause of long COVID. Furthermore, the same symptoms could be produced via an analogous mechanism by the COVID shot as well,” he added.

Burkhardt and Lang

The Palmer and Bhakdi paper says that Burkhardt and Lang studied many cases of people who died months or days after getting the COVID vaccine.

In all of these cases, the cause of death was documented as “natural” or “unknown.”

Some members of the families of those deceased had doubts about the verdicts of their causes of death and wanted to double-check.

According to the study, Burkhardt found “the majority of these deaths to be due to vaccination.”

The Epoch Times recently reported that several embalmers across the country have been observing many large, and sometimes very long, “fibrous” and rubbery clots inside the corpses they treat, and are speaking out about their findings. Some doctors believe them to be connected to the vaccines.

Toxic Components Found in COVID Jab; Vaccinated 5X More Contagious

Unusual Toxic Components Found in COVID Vaccines, ‘Without Exception’: German Scientists

By Enrico Trigoso
August 22, 2022 Updated: August 23, 2022

A group of independent German scientists found toxic components—mostly metallic—in all the COVID vaccine samples they analyzed, “without exception” using modern medical and physical measuring techniques.

The Working Group for COVID Vaccine Analysis says that some of the toxic elements found inside the AstraZeneca, Pfizer, and Moderna vaccine vials were not listed in the ingredient lists from the manufacturers.

The following metallic elements were found in the vaccines:

  • Alkali metals: caesium (Cs), potassium (K)
  • Alkaline earth metals: calcium (Ca), barium (Ba)
  • transition metals: cobalt (Co), iron (Fe), chromium (Cr), titanium (Ti)
  • Rare earth metals: cerium (Ce), gadolinium (Gd)
  • Mining group/metal: aluminum (Al)
  • Carbon group: silicon (Si) (partly support material/slide)
  • Oxygen group: sulphur (S)

These substances, furthermore, “are visible under the dark-field microscope as distinctive and complex structures of different sizes, can only partially be explained as a result of crystallization or decomposition processes, [and] cannot be explained as contamination from the manufacturing process,” the researchers found.

They declared the findings as preliminary.

The findings “build on the work of other researchers in the international community who have described similar findings, such as Dr. Young, Dr. Nagase, Dr. Botha, Dr. Flemming, Dr, Robert Wakeling, and Dr. Noak,” Dr. Janci Lindsay, Ph.D., a toxicologist not involved in the study, told The Epoch Times.

“The number and consistency of the allegations of contamination alone, coupled with the eerie silence from global safety and regulatory bodies, is troublesome and perplexing in terms of ‘transparency’ and continued allegations by these bodies that the genetic vaccines are ‘safe,’” Lindsay added.

Epoch Times Photo
Comparison of crystals in the blood and in the vaccine; on the left, crystalline formations are found in
the blood of test subjects vaccinated with Comirnaty (BioNTech/Pfizer), the images on the right show that these
types of crystals are also found in Comirnaty vaccines. (Courtesy of Helen Krenn)

Helena Krenn, the group’s founder, submitted the findings to German government authorities for review.

“We had submitted it to the participants of the government and further addresses from newspapers with the platform open-debate.eu, only in Germany, Austria, and Suisse,” Krenn told The Epoch Times.

Two other important findings were that blood samples from the vaccinated had “marked changes” and that more side effects were observed in proportion to “the stability of the envelope of lipid nanoparticles.”

A lipid nanoparticle is an extremely small particle, a fat-soluble membrane that is the cargo of the messenger RNA (mRNA).

Methodology

“Using a small sample of live blood analyses from both vaccinated and unvaccinated individuals, we have determined that artificial intelligence (AI) can distinguish with 100% reliability between the blood of the vaccinated and the unvaccinated. This indicates that the COVID-19 vaccines can effect long-term changes in the composition of the blood of the person vaccinated without that person being aware of these changes,” the study states.

The findings of acute and chronic physiological changes to the blood of those inoculated with the vaccines, consistently discerned via AI software, “also echoes the findings of many other researchers and support the contentions of contamination and/or adulteration,” Lindsay said.

“We have established that the COVID-19 vaccines consistently contain, in addition to contaminants, substances the purpose of which we are unable to determine,” their study says.

The group consists of 60 members, including physicians, physicists, chemists, microbiologists, and alternative health practitioners, supported by lawyers and psychologists.

Epoch Times Photo
Anomalous objects in Johnson & Johnson’s Janssen vector vaccine. It should be noted that objects of this
type were not found in all of the samples. (Courtesy of Helen Krenn)

The scientists claim that their results have been cross-confirmed using the following measuring techniques: “Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDX), Mass Spectroscopy (MS), Inductively Coupled Plasma Analysis (ICP), Bright Field Microscopy (BFM), Dark Field Microscopy (DFM) and Live Blood Image Diagnostics, as well as analysis of images using Artificial Intelligence.”

The analysts explain that they have been cooperating with other groups in different countries that have been executing similar investigations and have obtained results consistent with their own.

“The results from our analysis of the vaccines can, consequently, be regarded as cross-validated,” the summary report of their findings states.

“It should be acknowledged of course that [German Working Group’s] work is described as ‘Preliminary Findings,’ not yet published in a peer-reviewed journal and that chain of custody as well as the identity of many of these scientists is unknown. However, in this heavily charged and censored climate when it comes to any challenges to the ‘safety and efficacy’ of the genetic vaccines, I myself can attest to the difficulties in conducting the basic research, much less publishing that same research in a peer-reviewed journal, in order to get at these questions as well as disseminate the findings,” Lindsay said.

Epoch Times Photo
The Comirnaty vaccine from BioNTech/Pfizer exhibits a diversity and large number of unusual objects.
The vast number of crystalline platelets and shapes can hardly be interpreted as impurities. They appear regularly
and in large numbers in all samples. (Courtesy of Helen Krenn)

Astra Zeneca, Moderna, Pfizer, and J&J did not respond to a request for comment


Study: Vaccinated 5X More Contagious Than the Unvaccinated 10 Days After SARS-CoV-2 Infection

 

35-Year-Old Hiker Dies Suddenly on Thomas Lakes Trail outside of Carbondale, CO

“A 35-year-old man died Aug. 12 after passing out while hiking the Thomas Lakes Trail with his girlfriend, who tried to resuscitate him with instructions from Pitkin County dispatchers.

Thomas Lakes Trail is a 7.8-mile out-and-back trail just outside of Carbondale. The trail is popular with hikers looking for a relatively easy day-hike and backpackers seeking to summit Mt. Sopris.

Law enforcement officers say the man may have experienced a cardiac event.”

https://www.summitdaily.com/news/hiker-dies-on-thomas-lakes-trail-outside-of-carbondale/


CDC Admits Dramatic Mistakes in COVID Response;  Sen. Ron Johnson: Pandemic Politics & America’s COVID Cartel; Fauci Stepping Down

CDC Admits Dramatic Mistakes in COVID Response
Sen. Ron Johnson: Pandemic Politics & America’s COVID Cartel

How Doctors Detect COVID

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Fauci Announces He’s Stepping Down as NIAID Director, Medical Adviser to Biden

By Zachary Stieber
August 22, 2022 Updated: August 22, 2022

Dr. Anthony Fauci is stepping down from three government positions he holds, he announced on Aug. 22.

Fauci is resigning as director of the National Institute of Allergy and Infectious Diseases (NIAID), chief of the NIAID Laboratory of Immunoregulation, and chief medical adviser to President Joe Biden.

The moves will take effect in December, Fauci said.

He indicated that he will leave the government, but not retire.

“While I am moving on from my current positions, I am not retiring,” Fauci said. “After more than 50 years of government service, I plan to pursue the next phase of my career while I still have so much energy and passion for my field. I want to use what I have learned as NIAID Director to continue to advance science and public health and to inspire and mentor the next generation of scientific leaders as they help prepare the world to face future infectious disease threats.”

Fauci, 81, has repeatedly hinted he would step down from his positions, but has not committed before to a specific time for resigning.

Republicans have vowed to investigate Fauci and other architects of U.S. pandemic policy if they gain control of either or both congressional chambers in the upcoming midterm elections.

“Dr. Fauci is conveniently resigning from his position in December before House Republicans have an opportunity to hold him accountable for destroying our country over these past three years,” Rep. Andy Biggs (R-Ariz.) said in a statement.

Longtime Government Official

Fauci has directed the NIAID since 1984. He has advised Biden since he took office in 2021, and was one of President Donald Trump’s chief advisers on the COVID-19 pandemic.

Fauci has drawn ire for recommending lockdowns as a bid to slow the spread of the virus that causes COVID-19, acknowledging he deliberately misled the American public on mask-wearing, and defending NIAID funding for the laboratory in Wuhan, China, that is located near where the first COVID-19 cases occurred.

Supporters say Fauci has been a voice of reason during the pandemic and that his positions have evolved as the science has developed.

NIAID is part of the National Institutes of Health (NIH).

Dr. Lawrence Tabak, the acting director of the NIH, said in a statement that Fauci is “the model public servant” and “is always guided by the science.

“It’s been an extraordinary privilege and honor to have worked by his side and to have learned so much from him—I will miss him greatly. But I also look forward to seeing what Tony will do next. I have no doubt that he will continue to have an enormous impact on the world,” Tabak said.

 

The People Are Overwhelming Deep State; Situation Update; New Book Challenges COVID-19 Vaccine Narrative

Flynn/Clark – Information War, The People Are Overwhelming The [DS], We Are Taking Back Our Country

Situation Update

 

New Book Challenges COVID-19 Vaccine Narrative

BY KRISTEN FISCHER TIMEAUGUST 17, 2022 PRINT

As more research is published on people who have taken the COVID-19 vaccine, more data—at least the data that make it to publication—are revealing that many people have had harmful effects from the injections.

Of course, COVID-19 itself came with health consequences, and everyone understood that. The vaccine was supposed to be so safe and effective that it was acceptable to even coerce people into getting it. In fact, even those who caught COVID-19 and achieved natural immunity were compelled to get the vaccine.

In her latest book “Neither Safe Nor Effective: The Evidence Against the COVID Vaccines,” Dr. Colleen Huber shares some of the data that have been emerging.
Epoch Times Photo
Dr. Colleen Huber, naturopathic medicine doctor. (Courtesy of Dr. Huber)

The Arizona-based naturopathic medical doctor says the damage done so far from the mRNA vaccines is undeniable. She also highlights issues in the medical and media fields that have kept people from getting access to facts. This all comes as many people are still being pressured to take the vaccine or are suffering consequences.

Huber encourages people to pick up the book and to think for themselves while reading it.

“You won’t get past chapter one without being convinced that these vaccines shouldn’t be used on anyone, because of all the damage that has been seen in vaccinated populations,” she said.

Examining Vaccine Effects

In the book, Huber discusses how mRNA is the culprit behind the risks and damage in people. The technology had never been used safely in the past. It’s always had “wildcard dangerous effects in the body,” she said.

The mRNA mechanism sets in motion a process that can affect the DNA of the person and impact multiple organs in unwanted ways.

For example, a Swedish study published this year shows that the Pfizer vaccine enters the DNA of liver cells within six hours.

“This, in turn, changes how the DNA of the body produces new proteins,” Huber said. “In other words, the liver of a vaccinated person is gradually becoming different, and it is too early to know how and to what extent.

“The liver is responsible for hundreds of metabolic functions, so this is one of many reasons why taking these vaccines is so horribly reckless.

“We cannot yet be certain about this happening in other organs, because that research hasn’t yet been done, and this, again, is because the technology is still so new.”

Based on data she reviewed from the United States, Europe, and Israel, Huber said there are demonstrated cardiovascular injuries such as heart attack, cardiac arrest, myocarditis, and pericarditis.

Other common side effects were neurological injuries such as Bell’s palsy and seizures, new and aggressive cancers, and liver diseases.

In the book, Huber focuses on evidence of the first three adverse effects, because they were “by far the most thoroughly documented, and the least deniable,” she said.

Epoch Times Photo

The book includes data presented by Pfizer and the FDA under court order (after a lengthy back-and-forth battle). The data show that of the 30,096 people in the clinical trial (and an additional 2,990 on whom they have no data), there were 1,223 deaths and 11,361 people who had “not recovered at the time of report.”

It’s too early to know the effects of the vaccine, especially in those who got the initial vaccine (or two-dose vaccines) but didn’t get the boosters. Some people who had the initial vaccine and had some adverse effects took ivermectin, vitamin D, N-Acetyl Cysteine (NAC), and pine needle tea for relief. Ivermectin gives the best results, Huber believes, because it has known mechanisms against the spike proteins.

More Jabs, More Damage?

Huber believes that the more vaccines (or “boosters”) a person gets, the more damage that can be done.

She highlights data from the United Kingdom that show an especially high COVID death rate there. The U.K. is one of the most heavily vaccinated countries in the world, with 92 percent of people older than age 12 vaccinated.

The poorer outcomes, she believes, are linked to more mRNA being added to the body “in order to churn out even more of the devastating spike proteins into the cardiovascular system.”

Setting Records Straight

In addition to issues surrounding the quality and suppression of data, there’s also conflict about research that get published and those that never make it into journals (and, therefore, the mainstream media).

Huber echoes Dr. Peter McCullough, a well-known cardiologist who has sounded the alarm on how journals have suppressed research on early treatments for COVID-19.

Huber said that it’s hard to get her hands on data, especially if the data have never made it to publication.

“Governments in one country after another, first the U.S., then the UK and Scotland, which had collected the most data, suddenly hid data,” she said.

Unmasking the Medical Community

If the vaccines were so harmful, why did so many doctors pressure patients to take them?

“Doctors are threatened in many ways by rogue and frequently lawbreaking medical boards—the domineering antagonists to the passive doctors—to ‘shut up and do what we tell you,’” she said, citing her own experience.

“Few doctors have the time, energy, bandwidth, or, frankly, the ‘cojones’ to rebel against the bureaucrats.”

If the general trend of the medical profession is to recommend COVID vaccines, and if threats are made against any who would choose to rebel, you will find a majority going along, Huber said.

“That is, until the tide turns. When the tide begins to turn,” she said, “it’s much easier for an individual doctor to move with the herd against bad medical treatments, such as the COVID vaccines.”

She said many doctors are no longer pressuring patients to get the vaccines.

“And it all seems to be happening at once, at least in pediatrics and cardiology,” she said.

“When the flock of birds turns and starts flying in a different direction, each bird turns in cooperative, almost choreographed, synchrony.”

Huber compares the shift to that which occurred with the pain-relieving drug Vioxx. In the early 2000s, it was highly recommended. But in 2007, the harms of the drug were exposed, and doctors stopped prescribing it.

Now, avoiding that drug is “not at all controversial,” she said. “No medical board punishes a doctor for avoiding Vioxx.”

Time to Serve Your Country; They Want Your Children; Nuremburg Code; Situation Update;  Australian Government is Put on Notice by Medical Professionals

AustraliaOne Party – An Oath to Serve Your Country (Edited)


‘They want your land, they want your gold and they want your kids. These are the real assets they are after.’ – Catherine Austin Fitts

Watch FULL EPISODES of ‘Financial Rebellion’ With Catherine Austin Fitts on CHD.TV
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75th Annual Commemoration of the Nuremberg Code

“It was almost 75 years ago that the city of Nuremberg was the place of a historic declaration. When the judges of the military tribunal against leading medical officers in the Nazi administration passed their verdict, they issued what would become known as the Nuremberg Code.

On August 20, a compelling line-up of international speakers will travel to Nuremberg to commemorate the 75th Anniversary of The Nuremberg Code. Now of all times, in its jubilee year, this achievement of mankind is facing the greatest hardship since it was written. WATCH the historical event LIVE at 7am EST | 1pm CET | 4am PST or catch the replay at: 75th Annual Commemoration of the Nuremberg Code


Situation Update: Published August 18, 2022


JPMorgan Gold Traders Found Guilty After Long Spoofing Trial
RNA for Moderna’s Omicron Booster Manufactured by CIA-Linked Company


 Australian Government is Put on Notice by Medical Professionals

TO: The Australian Colleges and Associations of Medicine, Health, and Science, and All Australian Federal, State, and Territory Senators and Members of Parliament

 

Dear Colleagues,

 

It is with great pleasure that I introduce you and your respective organisations to the Australian Medical Professionals Society. This email deals with several issues which are of concern to our membership and, we hope, yours. At the top of the list is the issue of medical free speech and its ramifications for true dialogue, debate, and informative patient interaction in Australia. Also, this email and the report of Dr Phillip Altman, makes available to you and your members a cutting edge update on the COVID-19 vaccinations and a comprehensive analysis of associated Adverse Events, together with implications for Australian practice. Finally, we draw your attention to our Health Reform Declaration, a statement which is gaining support as it highlights critical issues and potential solutions, within the complex environment of Australian Health Law.

Australian Health Professionals and Scientists have been actively discussing and contemplating the profound health measures undertaken within Australia over the last 2&1/2 years. However, we believe the current range of medical, medicolegal and medicopolitical issues brought about by the pandemic requires a greater breadth of discussion – not less – within and between our respective organisations and memberships.

One of the chief concerns of our membership is that of medical free speech. Contingent to a joint statement received from AHPRA and the National Boards on 9 March 20211, Australian Health Professionals numbering over 825,000 were essentially forbidden from publicly questioning the science underlying the emerging COVID-19 injectables, let alone questioning any government messaging urging Australians to be vaccinated because these products were deemed ‘safe and effective’. The effect of this unilateral action was to undermine professional independence and, in so doing, strip away years of training, academic achievements, qualifications, awards and expertise. However well intentioned, this gagging by bureaucratic decree inserted AHPRA and the National Boards between the Clinician and their Patient, in addition to counteracting normal robust interprofessional dialogue, as more data emerged.

Indeed, now 17 months later and after numerous forms of pressure to take up the COVID-19 injectables in various age categories, a tremendous amount of data is available to more fully and accurately inform clinicians about these products. This literature includes over one thousand2 peer reviewed studies reporting of the harms being seen around the world, up to December 2021. In addition, it has become clear that the risk of serious illness and death attributable to COVID-19 disease is heavily weighted to the elderly and those with known co-morbidities, while in contrast, younger Australians are relatively resistant. Also, since the advent of the Delta and Omicron variants, it is highly questionable whether the vaccines are preventing transmission or illness.

In any event, the implied and intended outcome of the gagging was to see Doctors and Health Professionals effectively mandated to support the government campaign to have the Australian population injected with drugs for which there was no adequate short-, medium-, or long-term safety or efficacy data. Indeed, the rush to market and Provisional Approval occurred despite the absence of the usual pre-clinical studies, including testing for Carcinogenicity and Genotoxicity. In this regard, it should be of serious interest that a peer-reviewed investigation3 has demonstrated that mRNA-derived Spike proteins enter the cell nucleus and interfere with DNA. However, many critical facts like these became forbidden subjects for Health Professionals and Doctors to raise with their patients, let alone in public forums. Thus, we contend that the joint statement of 9 March 2021 has compromised proper and informed consent in Australia.

Especially given the lack of available pre-clinical research for each of these products, or clinical studies powered to detect early safety signals at the time of Provisional Approval, the need for ongoing critical appraisal of pharmacovigilance data remains paramount, to instruct responsible day to day practice. To date, none of the makers of the COVID-19 injectables have been able to stringently show their products to be Safe or properly Effective. To date, Adverse Events flowing from these products are at historically unprecedented levels globally and continue to rise. And again, to date, no other drugs in human history have reported more deaths, illnesses, injuries, and disabilities, which number as follows (to 28 June 2022):

 

It is widely acknowledged that all Adverse Event reporting systems suffer from under-reporting12, an inherent challenge for passive reporting systems and their interpretation. For US VAERS reporting in respect of the COVID-19 injectables, the Under-Reporting Factor (URF) has been estimated to be between 40-49x13. If a conservative URF of 10x is applied, the above figures begin to more realistically represent the likely true effects of the Covid-19 injectables:

 

To be clear, the TGA has received more Adverse Event reports in 2021 through June 2022 for the COVID-19 vaccines, than they have been seen for all other vaccines in the preceding 50-year period. A similar explosion in Adverse Event reports for the COVID-19 injectables has occurred in all other countries that chose to deploy them14, but in Australia, comparing the period from 197115 until the start of 2021 in respect of traditional protein-based vaccines, to the period from 1 February 2021 through 8 June 2022 in respect of the COVID-19 injectables, we observe the following:

To assist your organisation and membership to understand the causes leading to these concerning signals, we provide to you the comprehensive and up-to-date report of Dr Phillip Altman. By way of background, Dr Altman’s report has been used in modified formats to assist judiciaries in Australia and New Zealand to understand the scientific evidence behind the COVID-19 injectables. We believe it is proving to be the long-awaited body of work needed by the Judicial, Medical, and Scientific communities of Australia, to bring clarity by critical scientific appraisal during these controversial times of COVID-19.

 

Since your organisation is now in possession of the information and resources contained in the linked report, we ask that your members also receive the same for the benefit of their being fully informed as to the state of the science surrounding COVID-19. After considerable consultation, AMPS is of the opinion that Australia is experiencing a highly significant iatrogenic event. Further, we believe that this did not have to occur: it could have been avoided, but for the state of Australia’s health law leading into the pandemic. AMPS is strenuously of the view that in order to avoid a repeat of the recent past, Australian health law requires urgent reform. To this end we invite every organisation receiving this email, including every parliamentarian CC’d, to review the Declaration and Urgent Demands for healthcare law reform set forth on the following page:

https://amps.redunion.com.au/healthreformdeclaration

On the above Declaration page is also found Proposed Amendments to the Health Practitioner Regulation National Law, and Proposed Amendments to the Therapeutic Goods Act.

Many organisations receiving this email have members who are directly affected by the overarching powers of AHPRA and the National Boards, who have tended to dictate rather than consult with their registered members. This has caused a dangerous interference with the provision of information, for the purpose of each Australian exercising their right to fully Informed Consent, while it has also unduly and harshly seen Health Professionals sanctioned for seeking to uphold ethics and their Codes of Conduct.

It is not only regarding COVID-19 that AHPRA has been perceived to show over-reaching powers. Dissatisfaction and fear of AHPRA is widespread amongst many health professionals as evidenced by the Victorian branch of the AMA calling for a Royal Commission16 into AHPRA’s conduct.

Equally, we say it is evident that Australians have suffered as a consequence of the Provisional Approval pathway laws. These have facilitated the rapid entry of significantly undertested products into the Australian market, despite their being recognised to be highly novel and experimental. Nonetheless, the COVID-19 injectables were mandated in many jurisdictions and workplaces, causing large numbers of Australians to feel coerced and simultaneously baffled by the inability of Doctors and other Health Professionals to give them a voice.

This can all be changed.

We implore you as fellows and colleagues to give the information and resource contained in this email your greatest attention, with a view to sharing the same with your members. There will doubtless be many questions arising from our email and we invite further discussion with you. All of your considerations and efforts towards the continued promotion of evidence-based medical science are greatly appreciated.

Yours sincerely,

Associate Professor Christopher Neil

MBBS, FRACP, PhD

Incoming President

Australian Medical Professionals Society

 

[1] https://www.ahpra.gov.au/News/2021-03-09-vaccination-statement.aspx

[2] https://www.covidmedicalnetwork.com/coronavirus-facts/vaccine/4_5902465845702954112.pdf

[3] https://www.mdpi.com/1467-3045/44/3/73/htm

[4] https://www.adrreports.eu/en/covid19_message.html – Pfizer, Moderna, AstraZeneca, Janssen

[5] Individual reports refer to a single patient, where more than one adverse reaction is often included.

[6] https://openvaers.com/covid-data (only US/Territories) – Pfizer, Moderna, AstraZeneca

[7] Individual reports refer to a single patient, where more than one adverse reaction is often included.

[8] https://www.tga.gov.au/periodic/covid-19-vaccine-weekly-safety-report-23-06-2022 – Pfizer, Moderna, AstraZeneca

[9] Individual reports refer to a single patient, where more than one adverse reaction is often included.

[10] https://www.gov.uk/government/publications/coronavirus-covid-19-vaccine-adverse-reactions/coronavirus-vaccine-summary-of-yellow-card-reporting – Pfizer, Moderna, AstraZeneca

[11] Individual reports refer to a single patient, where more than one adverse reaction is often included. The 458,463 reports received to 24 June 2022 reported a total of 1,495,273 various forms of adverse reaction.

[12] https://scholar.google.com.au/scholar?hl=en&as_sdt=0%2C5&as_vis=1&q=EMA+ADR+under-reporting&btnG=

https://vaers.hhs.gov/data/dataguide.html

[13] https://stevekirsch.substack.com/p/latest-vaers-estimate-388000-americans

https://jessicar.substack.com/p/the-true-under-reporting-factor-urf

[14] https://worldcouncilforhealth.org/resources/covid-19-vaccine-pharmacovigilance-report/

[15] See DAEN website for no. of adverse events non-COVID vaccines and Covid injectables.

[16] https://insightplus.mja.com.au/2022/27/ama-victoria-to-call-for-royal-commission-into-ahpra/

AMPS – Australian Medical Professionals’ Association
P: (07) 3497 5048 | hotline@amps.asn.au | www.amps.asn.au 

Toxins in Vitamins; New CDC COVID-19 Guidance; Orange Man Bad; Make America Great Again

Toxins in Your Children’s Vitamins

New CDC COVID-19 Guidance Is Agency ‘Admitting It Was Wrong’: Epidemiologist

By Zachary Stieber and Jan Jekielek

 

August 13, 2022 Updated: August 13, 2022

The new Centers for Disease Control and Prevention (CDC) COVID-19 guidance is the agency acknowledging it was wrong in the past to downplay natural immunity and promote unprecedented policies like asymptomatic testing, a California epidemiologist says.

The new guidance, released on Aug. 11, rescinds and alters a number of key recommendations, including treating unvaccinated and vaccinated people differently for many purposes, explicitly stating that people with previous infection have protection against severe illness, and removing six-foot social distancing advice.

“The CDC is admitting it was wrong here, although they won’t put it in those words,” Dr. Jay Bhattacharya, professor of medicine at Stanford University School of Medicine, told The Epoch Times.

“What they’ll say is that, well, ‘the population is more immunized now, has more natural immunity now, and now is the time—the science has changed.’”

But a large percentage of the U.S. population has had natural immunity, or protection from prior infection, Bhattacharya noted, while over 80 percent of the elderly population had protection from severe disease from COVID-19 vaccines, previous infection, or both, since 2021.

“This is two years too late, but it’s a good step,” Bhattacharya added.

CDC Statement

The CDC, which did not respond to a request for comment, portrayed the change as streamlining previous guidance, with the adjustments stemming from more people being vaccinated and more COVID-19 treatments available.

“We’re in a stronger place today as a nation, with more tools—like vaccination, boosters, and treatments—to protect ourselves, and our communities, from severe illness from COVID-19,” Greta Massetti, the CDC author of the new guidance, said in a statement. “We also have a better understanding of how to protect people from being exposed to the virus, like wearing high-quality masks, testing, and improved ventilation. This guidance acknowledges that the pandemic is not over, but also helps us move to a point where COVID-19 no longer severely disrupts our daily lives.”

Dr. Jerome Adams, the surgeon general during the Trump administration, echoed the line of thinking.

“The fact that @CDCgov is changing guidance shouldn’t be taken as proof that they were necessarily ‘wrong,’ on a particular issue. The virus has changed, our tools and immunity have changed, and our knowledge has changed. So too must our guidance. That’s how science works,” Adams wrote on Twitter.

Vaccination numbers have fallen off in recent months, with little change among adults and little update among children, even after the vaccines were authorized and recommended for kids as young as 6 months old.

No new treatments have been authorized since December 2021, and a number of the treatments have been shown as less effective against newer strains of the virus that causes COVID-19, as have the vaccines and, in some cases, natural immunity.

Nearly half of the 20 papers and briefs cited by the CDC in support of the adjusted guidance were published in 2020 or 2021, while a number of others were released in early 2022.

No Mandates Rescinded Yet

Among the most significant changes in the guidance: a rollback of recommendations for asymptomatic testing for individuals exposed to COVID-19, loosening guidance related to tracing contacts of COVID-19 cases, and ending quarantine recommendations for people exposed to a positive case.

Some rules are stricter for high-risk settings such as nursing homes.

Masking is also recommended for 10 days for people who were exposed to COVID-19, including when a person is at home around others.

Bhattacharya, who co-authored the Great Barrington Declaration in 2020, a document that called for focused protection on the elderly and fewer restrictions on others, said that the guidance is closely aligned with the principles outlined in the declaration.

Based on the new guidance, the CDC should immediately rescind the COVID-19 vaccine mandate for foreign travelers entering The United States, a policy imposed in November 2021, the professor added.

The CDC’s webpage describing the mandate says that the agency “is reviewing this page to align with updated guidance.” The U.S. government has not adjusted or rescinded any of its vaccine mandates since the guidance was changed.


People are sadly so brainwashed they have lost all concept of reality


It is up to US to make America Great Again

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