Coronavirus

https://childrenshealthdefense.org/d...9-74d068e4f1cb


05/26/22

Dr. Ryan Cole: ‘The Shots Need to Stop’

Pushing the gene-based COVID-19 vaccine on an entire population made no scientific sense, Dr. Ryan Cole told host Brian Hooker, Ph.D., on CHD.TV’s “Doctors & Scientists.”

By
Children's Health Defense Team
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“A pathologist is the quality control of medicine,” Dr. Ryan Cole told Brian Hooker, Ph.D., on a recent episode of CHD.TV’s “Doctors & Scientists.”

Cole is the founder, chief medical officer and laboratory director of Cole Diagnostics, an independent medical laboratory in Garden City, Idaho.

He joined Hooker to discuss the pathology of COVID-19, changes in pathological patterns he saw during the rollout of the COVID-19 jab, and speaking the truth while standing for true science.

In the pre-COVID era, Cole’s daily routine included evaluating biopsies, Pap smears, and other samples while overseeing microbiology and molecular biology labs. He also was responsible for overseeing bloodwork, analyzing data patterns and consulting with doctors and clinicians about tumors and infections.

It was apparent to Cole from the beginning of the COVID-19 pandemic that SARS-CoV-1 affected primarily the elderly and those with comorbidities. Society overreacted despite these early signals, he said.

Cole told Hooker he was extremely concerned when vaccines for the COVID-19 virus were proposed because it was “completely against what good science indicated.”

Hooker asked Cole, “As the vaccine was rolling out, what were you seeing in the pathology laboratory?”

Cole said before the vaccine, he saw plenty of sick patients and his lab swabbed and processed more than 150,000 COVID-19 specimens. However, after the COVID-19 shot rolled out in December 2020, he started to see an unusual change in patterns under the microscope.

When he started noticing distinct childhood viruses appearing in adult pathological cultures, Cole attributed this to immunosuppression as a result of the spike protein in the COVID-19 jab.

Several months after the rollout of the vaccine, Cole became extremely concerned about a surge in rates of endometrial cancer and other cancers, noting the patterns were congruent to the rollout of the shot.

He told Hooker the “smoking gun” came when he testified in a Senate committee this year with Sen. Ron Johnson (R-Wis.). At the meeting, a whistleblower came forward with the epidemiology database for the U.S. Department of Defense (DOD), which showed an uptick in various cancers.

Cole said the DOD then “froze” the epidemiology database and altered four to five years of data, an act which will inevitably generate “legal wranglings and investigations.”

“It’s almost Watergate-esque,” Cole said. The DOD changed data from 2016 to 2020 to make the 2021 data look as if they were not as bad as they really were, he said.

Cole and Hooker discussed how immunosuppression is induced by the COVID jab.

“Is this something that could have been anticipated and screened for in a normal clinical trial?” Hooker asked.

“Absolutely,” Cole said.

He explained that because the COVID-19 jab is a gene product rather than a true vaccine, the U.S. Food and Drug Administration (FDA) should have reviewed the jab as a gene-based therapy, not a traditional vaccine.

Adverse effects from the shot could have been anticipated, he said, if COVID-19 jab researchers had performed the animal studies that are routinely done for FDA-approved gene-based products on the market.

“To push a gene-based product like this onto an entire population with no idea what the long-term sequelae [will] be made no scientific sense whatsoever,” Cole said.

Hooker and Cole discussed the phenomenon of fibrous clots in living patients and cadavers. These are not typical blood clots, they said. Cole said these clotting problems also could have been anticipated in proper animal studies.

Cole pointed out the shots that are on the market were made for the Wuhan virus. He said he asks people two questions: “Is Wuhan [virus] present in humanity?” and “Do the shots cover Omicron?”

The answers are “No, it’s extinct,” and “No, they don’t.”

“The shots need to stop because of these clotting pathways, immune suppression and cancer-inducing pathways,” Cole said. “They’re all risk with no benefit at this point.”

Hooker also asked Cole about the reproductive consequences of lipid nanoparticles in the ovaries and if he was seeing these issues in the laboratory.

Cole said in his laboratory he witnessed an increase in decidual cast shedding, a typically rare phenomenon that increased tremendously during the COVID-19 pandemic.

He noted that in many studies claiming no reproductive risk with the shots, the abstract and conclusion do not match the data.

Cole also talked about his theories of spike protein shedding, grounding his hypotheses in the literature of the Pfizer application for emergency use and other studies that established the use of self-spreading vaccines for population control in rabbits.

When Hooker and Cole discussed the FDA’s approval of remdesivir for emergency use in babies as young as one month, Hooker stated, “Remdesivir is a huge problem; it is all downside, no upside.”

Cole added that in animal trials, up to one-third of animals experienced kidney failure after being injected with remdesivir.

Even though the World Health Organization criticized the use of remdesivir in 2020 due to its toxic effects and no survival benefit, “hospitals receive a 20% bonus on the hospitalization” if they treat a patient with the drug, he said.

“There is a huge financial incentive to administer remdesivir,” Cole said, despite the existence of many other safe therapeutics for COVID-19.

Hooker and Cole commended colleagues such as Dr. Peter McCullough and Dr. Paul Marik, who saved the lives of countless patients by using therapeutics during the first months of COVID-19. They agreed the focus from the beginning should have been on adequate therapeutics.

“What has been the response to you telling the truth regarding COVID-19?” Hooker asked Cole.

Cole said he has been attacked by the media, the American Board of Pathology and the College of American Pathologists.

Yet everywhere he goes, he said, he is thanked by countless doctors, families and patients for sharing the truth.

“With what I know, the knowledge I’ve been blessed with, the thousands upon thousands of papers that I’ve read and the patterns I’ve seen in the lab, to only help humanity … is my job,” said Cole.

“That’s my calling, that’s what I do,” he said.

Watch the episode here:

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video also on Rumble

https://rumble.com/v167cvu-doctors-and-scientists-episode-30-interview-with-stephanie-seneff.html

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Much about vaccines and Dr. Michael's Yeadon's recent show Posted here with him in this week's 5-27-22 news wrap-up show.https://usawatchdog.com/wp-content/u...-2-300x214.jpg


Mysterious Vax Deaths?, Gun Control Diversion & Food Crisis

By Greg Hunter On May 27, 2022 In Weekly News Wrap-Ups 3 Comments

By Greg Hunter’s USAWatchdog.com

(WNW 531 5.27.22)

Every week we are seeing what the legacy/mainstream media describe as “mysterious deaths” or “died suddenly.” There is no other explanation ever given. The latest is actor Ray Liotta who “suddenly” dies in his sleep. As a reporter, the question is a simple why? What is the cause of death? Sometimes you get the family wanting “privacy.” It’s almost a sort of “Stockholm Syndrome” where the victims protect their abusers. In this case, is it the vax makers? Does it have something to do with the global experiment of so-called CV19 vaccines? Does simply asking the question mean you are an “anti-vaxer” or a “conspiracy theorist”?

The school shooting in Texas took the lives of almost two dozen people, mostly children. The Democrats wasted no time in making gun control their new campaign rallying cry, and, thus, creating a huge diversion for all the problems they caused. I guess they cannot talk about out of control inflation, record fuel prices, a failing housing market, sky high rising crime, a wide open southern border and the real possibility of nuclear war they are trying to start with Russia. Hard to run on that. Instead, they want to run on killing less people with guns while they fight to kill babies with unrestricted abortion up until the day of birth. What a campaign platform!!!

There is no doubt a food crisis is coming with planting problems in the USA, a fertilizer shortage and war in Ukraine restricting the export of wheat. Russia wants to make a deal to stop the food shortage in exchange for what it calls politically motivated restrictions by the West. The response by NATO and the U.S. is to send more weapons and money to Ukraine to keep the war going. Count on higher and higher food and fuel prices for as far as the eye can see.

Join Greg Hunter of USAWatchdog.com as he talks about these stories and more in the Weekly News Wrap-Up for 5.27.22.

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video also on Rumble

48:13 runtime

https://www.youtube.com/watch?v=uWGTciX795o

https://www.youtube.com/watch?v=uWGTciX795o

How vaccines work against COVID-19: Science, Simplified

2:15 video runtime

1,075,554 views
Dec 18, 2020


Scripps Research
15.1K subscribers

After we have been exposed to an infection, our immune system remembers the threat, in particular by producing antibodies. These are proteins that circulate in the blood and throughout the body; they quickly recognize and disable the invader upon contact, thereby preventing or minimizing illness. This is why we usually do not get sick with the same bug twice; we are immune. Vaccines mimic this process, encouraging the immune system to make antibodies without us having to go through the illness.

Some of the leading SARS-CoV-2 vaccine candidates are “mRNA vaccines,” based on incorporating the genetic blueprint for the key spike protein on the virus surface into a formula that when injected into humans instructs our own cells to make the spike protein. In turn, the body then makes antibodies against the spike protein and they protect us against viral infection.
This strategy is faster than more traditional approaches, which often involve generating weakened or inactivated forms of a live virus or making large amounts of the spike protein to determine whether they can prompt an antibody response.

Once a potential vaccine is discovered, a number of checkpoints exist before it can be administered to people. First are preclinical tests, which involve experiments in a laboratory and with animals. Scientists must ensure the vaccine candidate is not only effective, but also safe. For example, an antibody response to an imperfect vaccine could, under extremely rare circumstances, end up increasing the danger of becoming infected.
When the potential vaccine achieves the necessary preclinical results, clinical trials can begin in a small group of people. As the vaccine candidate advances, it is tested on increasing numbers of people, with scientists and doctors closely monitoring safety, efficacy and dosing. Upon successful completion of clinical trials, the vaccine candidate must be reviewed and approved by regulatory agencies such as the FDA before large-scale manufacturing and distribution gets underway and the licensed vaccine is administered widely.

https://childrenshealthdefense.org/d...8-44a79b0d2748


05/27/22
•

COVID › News

Young Boy Died of Myocarditis After Pfizer Vaccine, Says CDC Before Signing Off on 3rd Shot for Kids 5-11

VAERS data released Friday by the Centers for Disease Control and Prevention show 1,277,980 reports of adverse events from all age groups following COVID-19 vaccines, including 28,312 deaths and 232,694 serious injuries between Dec. 14, 2020, and May 20, 2022.

By
Megan Redshaw

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The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,277,980 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and May 20, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 9,972 adverse events over the previous week.

VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 28,312 reports of deaths — an increase of 171 over the previous week — and 232,694 serious injuries, including deaths, during the same time period — up 2,330 compared with the previous week.

Excluding “foreign reports” to VAERS, 820,788 adverse events, including 13,045 deaths and 82,974 serious injuries, were reported in the U.S. between Dec. 14, 2020, and May 20, 2022.

Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.

Of the 13,045 U.S. deaths reported as of May 20, 16% occurred within 24 hours of vaccination, 20% occurred within 48 hours of vaccination and 59% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 583 million COVID-19 vaccine doses had been administered as of May 20, including 344 million doses of Pfizer, 220 million doses of Moderna and 19 million doses of Johnson & Johnson (J&J).

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Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.

Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.

U.S. VAERS data from Dec. 14, 2020, to May 20, 2022, for 5- to 11-year-olds show:

10,820 adverse events, including 285 rated as serious and 5 reported deaths.

22 reports of myocarditis and pericarditis (heart inflammation).

The CDC uses a narrowed case definition of “myocarditis,” which excludes cases of cardiac arrest, ischemic strokes and deaths due to heart problems that occur before one has the chance to go to the emergency department.

The Defender has noticed over previous weeks that reports of myocarditis and pericarditis have been removed by the CDC from the VAERS system in this age group. No explanation was provided.

43 reports of blood clotting disorders.

U.S. VAERS data from Dec. 14, 2020, to May 20, 2022, for 12- to 17-year-olds show:

31,762 adverse events, including 1,828 rated as serious and 44 reported deaths. VAERS reported 44 deaths in the 12- to 17-year-old age group last week.

63 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 96% of cases attributed to Pfizer’s vaccine.

652 reports of myocarditis and pericarditis with 639 cases attributed to Pfizer’s vaccine.

168 reports of blood clotting disorders with all cases attributed to Pfizer.

U.S. VAERS data from Dec. 14, 2020, to May 20, 2022, for all age groups combined, show:

20% of deaths were related to cardiac disorders.

54% of those who died were male, 41% were female and the remaining death reports did not include the gender of the deceased.

The average age of death was 73.

As of May 20, 5,542 pregnant women reported adverse events related to COVID-19 vaccines, including 1,736 reports of miscarriage or premature birth.

Of the 3,618 cases of Bell’s Palsy reported, 51% were attributed to Pfizer vaccinations, 40% to Moderna and 8% to J&J.

882 reports of Guillain-Barré syndrome, with 42% of cases attributed to Pfizer, 30% to Moderna and 28% to J&J.

2,301 reports of anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.

1,716 reports of myocardial infarction.

14,035 reports of blood-clotting disorders in the U.S. Of those, 6,283 reports were attributed to Pfizer, 5,020 reports to Moderna and 2,694 reports to J&J.

4,204 cases of myocarditis and pericarditis with 2,578 cases attributed to Pfizer’s, 1,428 cases to Moderna’s and 184 cases to J&J’s COVID-19 vaccines.

CDC acknowledges boy died of myocarditis, signs off on COVID for kids 5 to 11

A young boy between the age of 5 and 11 died after receiving his first dose of the Pfizer-BioNTech COVID-19 vaccine, according to the CDC.

Yet, the CDC’s vaccine advisory panel and its director, Dr. Rochelle Walensky, signed off on a third dose for the young age group despite their knowledge of the boy’s death.

Dr. Tom Shimabukuro, a member of the agency’s vaccine safety team, said during a virtual meeting held by the Advisory Committee on Immunization and Practices (ACIP) a young male died 13 days after receiving his first dose of Pfizer’s COVID vaccine.

The boy experienced a fever 12 days after his first dose. A day later, he experienced abdominal pain and vomiting. He passed away the same day. Evidence showed the boy suffered from heart inflammation known as myocarditis.

“This patient had a rapid clinical course. From the time they started experiencing their abdominal pain day 13 after dose one until the time they were brought into the [emergency department] and subsequently died was on the order of a couple of hours,” Shimabukuro said.

“Histopathological evidence of myocarditis was present on autopsy, and that was resolved to be the cause of death,” he added.

The death was reported to VAERS and verified by the CDC through an interview with the healthcare provider.

Tests conducted on the boy by the CDC’s infectious disease pathology branch “did not find evidence of viral infection at the time of death,” Shimabukuro said.

The ACIP did not ask questions or discuss the death, but instead, determined the benefits of Pfizer’s COVID vaccine outweigh the risks.

Family of 26-year-old who died 13 days after AstraZeneca shot weighs legal action

A final hearing began on May 23 in the investigation into the death of a 26-year-old man who died last year from “catastrophic” blood clots in his brain 13 days after receiving the AstraZeneca COVID-19 vaccine.

The family of Jack Hurn hopes the inquest will answer questions about the circumstances of his death — including why healthcare providers declined Hurn’s request for a Pfizer vaccine instead of the AstraZeneca shot, which is associated with blood clots in individuals under age 30.

Staff at the vaccine center where Hurn and his girlfriend received their vaccines allegedly told them the Pfizer vaccine was not available and assured them the AstraZeneca jab was safe.

Coroners in England and Wales must hold inquests in cases where deaths are sudden, unexplained or could have resulted from medical errors or negligence. The final hearing is expected to last three days.

A spokesperson for Portman-Hann’s law firm told the Daily Mail, “The family are looking at a clinical negligence claim but are waiting for the results of the inquest to decide on next steps.”

Increased risk of Guillain-Barré syndrome following J&J COVID vaccination

According to Neurology Advisor, the incidence of Guillain-Barré syndrome (GBS) was elevated following vaccination with the J&J’s COVID-19 vaccine — made by Janssen.

A new study published in JAMA Open Network analyzed Safety Datalink records of 10,158,003 people in the U.S. as of November 2021.

Researchers sought to evaluate the rate of GBS after receiving any COVID-19 vaccine. Incidence rates of GBS up to 84 days after vaccination were evaluated for each of the three vaccines — Pfizer, Moderna and J&J. Although both mRNA vaccines showed elevated incidence rates of GBS, in a head-to-head comparison, the J&J shot was associated with a higher incidence of GBS compared with the mRNA vaccines.

Risk-benefit analysis of Pfizer and Moderna COVID-19 vaccines in children and adolescents

As The Defender reported on May 26, an up-to-date document provides a comprehensive risk-benefit analysis of the use of the Pfizer and Moderna COVID-19 vaccines in children and adolescents.

It argues that the vaccines:

are not necessary, because the risk of severe disease or death due to COVID in children and adolescents is very low;

have not been proven efficacious in clinical trials, or in recently published studies on the now-predominant Omicron variant;

have not been proven safe; to the contrary, there is ample evidence of grave harm due to vaccination.

The document also addresses the risk of genotoxicity of the mRNA vaccines, which according to recent experimental evidence of their integration into host cell genomes, must be considered urgent.

Children’s Health Defense (CHD) asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

Suggest a Correction

Megan Redshaw is a staff attorney for Children's Health Defense and a reporter for The Defender.

Dr. Zelenko’s Interrogation



https://rumble.com/v15pz06-dr.-zelenkos-interrogation.html


How will he answer for his crimes against the narrative?
______________

Dr. Vladimir Zev Zelenko 05/23/22 Health Update

https://rumble.com/v15uwt1-dr.-vladimir-zev-zelenko-052322-update.html

Sunfellow on COVID-19 Published May 23, 2022 1,117 Views

Dr. Vladimir Zev Zelenko publishes an update on the status of his health from his hospital bed. May 23, 2022.

To learn more about Dr. Zelenko and The Zelenko COVID-19 Protocol, go here:

https://sunfellow.com/dr-vladimir-ze...d-19-protocol/

................

See Also:

Dr. Vladimir Zelenko – "Please Don't Live In Fear..."
https://rumble.com/vlkf94-dr.-vladim...n-fear....html

Dr. Zelenko Talks To Israeli Politicians And Health Minister About COVID Vaccines
https://rumble.com/vm0w7p-dr.-zelenk...-covid-va.html

Mercola & Zelenko: Treating COVID-19 & Healing Vaccine Damage
https://rumble.com/vlbara-mercola-an...ne-damage.html

The Zelenko COVID-19 Protocol
https://rumble.com/vl5xim-the-zelenk...-protocol.html

COVID-19 Healing Resources
https://sunfellow.com/covid-19-healing-resources/



How will he answer for his crimes against the narrative?

embedded video

DrVladimirZelenkoMD

Published May 22, 2022

327 rumbles

2:55 video runtime

Get Me Out of Twitter Jail With Z-Stack.

My team has been very busy in the past weeks. You may have seen my fun “interrogation video,” where Agent Joe Psaki of the now-defunct DHS Disinformation Board sentences me to life in Twitter jail. You can watch it here if you missed it: Dr. Zelenko’s Interrogation (rumble.com). I had a lot of fun making the video. If you like it, please share and we may make another one soon.

______________

Pray for Dr. Zelenko.

See a listing of Dr. Zelenko's video here

https://rumble.com/search/video?q=vladimir%20zelenko

https://www.youtube.com/watch?v=k6MTA2JBQB8

https://www.youtube.com/watch?v=k6MTA2JBQB8

'Why Did You Conclude That Religious People Can Be Singled Out?': Hawley Grills Biden Judicial Nom

May 11, 2022

Forbes Breaking News

At today's Senate Judiciary Committee hearing, Sen. Josh Hawley (R-MO) asked nominees about their judicial records.




Also Senator Blackburn on the same issue.

https://www.youtube.com/watch?v=kEDPX8Jxdiw

https://www.youtube.com/watch?v=kEDPX8Jxdiw

I am hoping that proof that FRAUD has been committed by the FDA and NIH and NIAID and the pharmaceutical companiest that made the "COVID" injectables.

What did they know and when did they know it?

Then the liability shield is no longer in effect and these entities can be disbanded and put out of business and all of the injured people and those who had to lose employment, such as airline pilots and all injured people and all military people who were unlawfully forced to take an unapproved "vaccine." I suggest damages be in the amount of one million dollars apiece to each injured person and a larger award for the families of persons killed by the experimental injectable and treatments in hospitals using EUA unapproved medicine and withholding known helpful approved medicines It was extremely reckless and dishonest to use an experimental mRNA technology that had never been tested on an EUA basis on humans. Immune defenses in the in the vaccinated individuals have been permanently changed and made less effective and the DNA of the vaccinated individual has been, according to more than one study, permanently changed.

__________________

Here is some good news.

https://www.zerohedge.com/covid-19/1...ccine-mandates

18 Major Airlines, FAA, And DOT To Be Sued Over COVID Vaccine Mandates

John Pierce Law has filed a lawsuit against Atlas Air, on behalf of US Freedom Flyers (USFF) and Atlas employees, and plans to sue all major airlines, 18 altogether, plus the Federal Aviation Administration (FAA) and the Department of Transportation (DOT), contending that the vaccine mandates imposed by these agencies on the airlines’ employees infringed on their constitutional, religious, and medical liberties.

The lawsuit against Atlas Air was filed in federal court in the Southern District of Florida, with over 100 plaintiffs pursuing litigation.

“Fundamentally, this case is about whether Americans should be required to choose between their livelihoods and being coerced into taking an experimental, dangerous medical treatment,” reads the lawsuit (pdf).

Plaintiffs are mostly unvaccinated pilots, flight attendants, as well as other Atlas staff.


___https://www.documentcloud.org/documents/22035148-usff-v-atlas-air-complaint-final

Dachssie comment:

Important information missing from this report. Describe the exact behavior that is said to have warranted subject being forcibly hospitalizedl.

I hope the offended party sues the FDA for enough money and retirement benefits to allow him to retire from employment comfortably. His employer is a hostile actor.
___________________




World Health Organization Temporarily Withdraws Biden’s ‘Public Health Emergency’ Amendments

https://www.thegatewaypundit.com/202...cy-amendments/

The World Health Organization withdrew 12 of the 13 amendments submitted by the Biden administration to alter the International Health Regulations at the World Health Assembly annual meeting, Reuters confirmed on Thursday.
The amendments would reform the International Health Regulations of 2005 to delegate U.S. medical sovereignty to the WHO during a “public health emergency” or outbreak.
Brazil, Iran, Malaysia and some African nations reportedly objected to incorporating the amendments and insists the modifications proposed by Biden should be consolidated in a new “Pandemic Treaty.”
Brazilian President Jair Bolsonaro was the only leader to oppose the pandemic treaty and rebuked Biden’s amendments, assuring his country would not surrender its sovereignty to the globalist institution.
e had to take care of the elderly and people with co-morbidities, and today studies outside of Brazil especially show that I was right.”




But the U.N. agency is slated to readdress Biden’s amendments at its upcoming meeting on June 16 to 17.
The WHO will also consider the separate Pandemic Treaty, which is currently being drafted, when it reconvenes on August 1.

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Pfizer CEO Albert Bourla explains to the WEF there's a surplus of 7,000,000,000 doses of his COVID vaccine sitting in warehouses because there aren't enough "educated populations that believe the vaccines are doing well.."
11:30 PM · May 26, 2022·Twitter Web App

embedded video in Tweet

https://twitter.com/i/status/1530043619545124871

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Dahsie comment:

"educated populations that believe the vaccines are doing well.."

We large numbers of people in the USA who still have a First Amendment are becoming educated, Mr. Bourla, and our belief system has become medicated with the truth.

https://www.dailywire.com/news/fda-o...thank-goodness

FDA Official In Charge Of Evaluating New Drugs Hospitalized For ‘Mental Disorder’

Lashes out that his "job carries a lot of responsibilities -- I'm an office director at FDA making major decisions every day that impact the public health."

https://dw-wp-production.imgix.net/2...ib=react-9.3.0

[SIZE=3]A top federal official in charge of evaluating the safety of drugs was hospitalized against his will this month for an unspecified “mental disorder,” prompting concern over his fitness for the role he said includes making “major decisions that impact on public health,” The Daily Wire has learned.

Dr. Jeffrey Siegel, director of the Food and Drug Administration’s Office of Drug Evaluation Sciences, was transported from his home to a hospital for “mental disorder” at 3 a.m. on May 9, according to Montgomery County, Maryland, police dispatch logs reviewed by The Daily Wire. Police declined to release a report on the incident despite a Freedom of Information Act request, but Siegel wrote about being taken from his home in a rambling note left on a neighborhood listserv.

“15 minutes later I saw bright red and blue lights (I may have the colors wrong) outside the house and then EMTs in our house who started to ask me to please come with them,” Siegel wrote in the note, more than a week after his hospitalization. “Thinking I was being asked to go voluntarily I politely declined. They insisted. Finally, they turned me around in the steps of my front hallway on Moorland Lane, handcuffed me, forced me unto a gurney, tied me down, took me in the ambulance to the hospital.”

One neighbor who received the missive via Nextdoor expressed concern about Siegel’s ability to do his job, given that Siegel also wrote that he makes ‘major decisions that impact on public health.'”

“I am frankly left a little bit worried for the soundness of operations at our FDA, if indeed that is true,” the neighbor wrote.

A biography of Siegel states that he leads the office that “oversees Clinical Outcome Assessments, Biomarker Qualification, Research and Bioinformatics” in the Office of New Drugs. An FDA org chart says that the deputy director position is vacant, and that he is also leading the “Division of Biomecial [sic] Informaci [sic], Research & Biomaker [sic] Dev.”

Siegel posted the note with pictures of bruised wrists, apparently sustained during a struggle with paramedics who were restraining him, complained about “brain fog,” and lashed out out a particular doctor for not giving him drugs he was seeking.

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Siegel did not respond to requests for comment.

In his note, Siegel boasted how his “job carries a lot of responsibilities.”

“Finally, I realized this was not voluntary but had been ordered by someone against my will… so I stopped resisting. When in the hospital I was given a clean bill of heath [sic] including CT and MRI and they sent me home on Tuesday with no diagnosis,” he wrote.

“Unfortunately, the problem didn’t end there. I had trouble sleeping so I asked [the doctor] for something to sleep. She refused,” he said. He claimed he paid her practice between $12,000 and $18,000 a year and asked “if anyone knows of a good lawyer (and I’m not the litigious type, but I feel I’m the injured party ]here).”

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Neighbors responded by questioning his account, with saying that someone had filed an “emergency petition” against him, and another speculating that it was his wife, not the doctor.

“This glass of juice has leaks in it, I would suggest a psychologist, rather than a lawyer. Good luck getting the mental health help you need,” another said.

Siegel, for his part, commented on the thread that he had “No COVID. Thank goodness.”

A Science.org article titled “FDA’s revolving door: Companies often hire agency staffers who managed their successful drug reviews,” published in 2018, reported that Siegel back in 2010 oversaw the approval of an arthritis drug from Genentech, and months later left the agency to join the company and represented it “before his former FDA colleagues when the company sought approval” to promote the drug for other conditions. He said the timing of his decision was coincidental.
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