‘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.”
The Centers for Disease Control and Prevention estimates that about 1 in 68 children are affected by autism – which is more than four times more common among boys. The causes of autism, however, are not yet fully understood.
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.
Dr Naviaux believes that suramin can ‘un-stick’ the cells by inhibiting the signal they release when they sense danger, which can help normalize the response.
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.”
Suramin was originally developed as a cure for sleeping sickness, a parasitic disease spread by the tsetse fly in sub-Saharan Africa.
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/
Syringes containing a COVID-19 vaccine in Needham, Mass., on June 21, 2022. (Joseph Prezioso/AFP via Getty Images)
EXCLUSIVE: FDA Withholding Autopsy Results on People Who Died After Getting COVID-19 Vaccines
By Zachary Stieber
September 29, 2022Updated: 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.
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.
FBI Whistleblower Comes Forward, Alleges Many Agents ‘Don’t Agree’ With Bureau’s Direction
By Jack Phillips
September 25, 2022Updated: September 25, 2022
An FBIwhistleblower recently came forward and issued warnings about alleged politicization at the FBI, saying that the bureau is spying on law-abiding Americans and that many of its domestic counterterrorism cases are tantamount to “entrapment.”
Kyle Seraphin, who has spent six years in the FBI, was suspended without pay and cannot seek another job without quitting or asking for permission. It’s not clear when he was suspended, but he said that he had run-ins with his managers about his refusal to get the COVID-19 vaccine although he was granted a religious exemption.
“The number of guys who say, ‘I don’t agree with what’s going on here, but I’ve got three years to retire,’ it’s heartbreaking,” he told podcast host Dan Bongino.
In one instance, Seraphin said he was forced to blow the whistle last year when Attorney General Merrick Garland told lawmakers that the Department of Justice was not targeting parents. He gave to a member of Congress an email that was circulated in the FBI, which said that Garland ordered the usage of the controversial PATRIOT Act to target parents with a tag, “EDUOFFICIALS.”
At the time, in May 2022, Reps. Jim Jordan (R-Ohio) and Mike Johnson (R-Ind.) alleged that the investigations involved parents who were “upset about mask mandates and state elected officials who publicly voiced opposition to vaccine mandates,” accusing Garland of making false statements to Congress.
“That’s when you become part of political hatchet jobs, and I didn’t sign up for that, and nobody I know signed up for that either,” Seraphin told Bongino. “That’s not what people want to get involved in.”
In an interview with the Washington Times last week, he said the bureau’s investigations into domestic violent extremism, white nationalists, and right-wing extremists are mostly entrapment operations with questionable moral and ethical underpinnings.
“My team was deployed to 20 or 25 different high profile, national terrorism organization or terrorism investigations between 2018 and 2021. And what I saw, as the most obvious statement, is that there are three things about counterterrorism investigations,” he said.
Seraphin stated: “Number one, the demand for white supremacy vastly outstrips the supply of white supremacy.”
“Number two,” he added, “the FBI‘s playbook when it comes to counterterrorism investigations is always and unequivocally morally equivalent to entrapment, even if there’s a legal definition that allows them to skirt that.”
As for No. 3, Seraphin added to the Washington Times that the FBI doesn’t have an objective metric on how they prioritize cases.
“There’s an entirely ridiculous internal process for determining every single national priority,” the whistleblower said.
The Epoch Times has contacted the FBI for comment. A bureau spokesperson told the paper that his claims about entrapment lacked merit.
“This comment is inaccurate and represents a clear misunderstanding of the policy and practice in FBI investigations,” the FBI said in a statement to the outlet.
In the Bongino interview, Seraphin suggested that more FBI employees will come forward in the future, according to him, due to the bureau’s now-partisan nature.
At least 14 FBI whistleblowers have come forward in recent months to provide information about recent actions inside the bureau, said Jordan, on the FBI’s investigations into the Jan. 6 Capitol breach, parents at school board meetings, and Hunter Biden’s laptop.
At one point during the interview, Seraphin also touched on the Aug. 8 raid targeting former President Donald Trump’s Mar-a-Lago. Trump has often said that the search was political in nature and meant to harm his 2024 chances.
“You ask me to go raid President Obama’s house, you ask me to raid President Bush’s house, it’s not happening,” he continued. “It’s not happening. I’m sorry, it’s not happening. I’m not doing that. I’m going to be, probably pretty vocal. That’s probably going to be my last day.”
Woman Escapes COVID-19 Hospital Treatment Protocols, Says Others Not So Lucky
By Matt McGregor
September 15, 2022Updated: September 15, 2022
Over a week after Gail Seiler’s physician had given her a terminal diagnosis, her husband, Brad Seiler, wheeled her out of the back door of the hospital where she had been admitted for COVID-19 on Dec. 3, 2021.
“I’m so sorry, Mrs. Seiler, but you are going to die,” she recalled her physician telling her on Dec. 5.
On Dec. 15, despite resistance from hospital staff, Brad extracted Seiler from Medical City Plano hospital in Plano, Texas, where the couple lives.
Seiler is one of the few patients who has lived to tell her story about what she said she witnessed on the inside with COVID-19 hospital treatment protocols.
“It became clear to me that people are not dying in hospitals from COVID. They are dying from these protocols,” Seiler told The Epoch Times.
Seiler went in for a monoclonal antibody infusion with the request that she be given the early-treatment protocols prescribed through the Front Line Critical Care Alliance (FLCCA), which included the use of ivermectin and budesonide.
However, when staff discovered she was unvaccinated, “the whole tone changed,” she said.
“I quickly lost the right to advocate for my own medical care,” she said.
‘I Didn’t Come Here to Die’
After a 26-hour wait, she finally got a bed in the intensive care unit (ICU), but no family members were allowed to visit, she said.
This is where she met Dr. Giang Quach, the physician who told her she was going to die because she was unvaccinated, she said.
“I told him, ‘I didn’t come here to die,’” she said.
Seiler said Quach pushed her to take Remdesivir, a drug known to cause kidney failure. She repeatedly asked for a different doctor, but her pleas went unanswered and Quach remained in charge of her care, she said.
In 2018, President Donald Trump signed the Right to Try Act into law, which allowed patients with life-threatening diseases who have exhausted all other options to try certain unapproved treatments.
Because Quach had given Seiler a terminal diagnosis, she was entitled to try FLCCA protocols to treat COVID-19, but the hospital denied her those treatments, she said.
Quach also denied Seiler her right to see a priest to administer her last rites, she said.
So, Seiler made a deal with Quach, she said.
She said she would submit to a round of remdesivir if Quach let her see her priest for final sacraments.
Quach agreed, and Seiler was allowed to see her priest, she said.
“Then, we denied the remdesivir,” Seiler said. “They were pretty angry about it, but honestly, I felt I was in a fight for my soul. When the priest left, I had this renewed feeling that I was going to live and not be killed.”
‘Every Day I Would Tell Them I’m Not a DNR’
Every day, Seiler said, she made it known that she did not want Quach in charge of her care and insisted on seeing a different provider, but Quach always returned.
Seiler’s daughter had access to her online records, where she found that Seiler was classified as Do Not Resuscitate (DNR), she said.
Seiler said she was not supposed to be listed as DNR.
“The scariest part of it was every day I would tell them I’m not a DNR, but them telling me I’m a DNR,” Seiler said.
In order to be resuscitated, Seiler said, hospital staff told her she had to go on the ventilator, the final stage for many who have reported similar hospital stories that ended in death.
Each of the standard treatment protocols for COVID-19, beginning with remdesivir and ending with the ventilator, are reimbursed with lucrative payoffs from the Centers for Medicare and Medicaid Services (CMS), leading many to believe this is the reason hospitals continue to use these protocols while denying early treatment.
In a Sept. 7 conference titled “Remdesivir Death: Landmark Lawsuit” in Fresno, California, two attorneys announced lawsuits against three hospitals for what they allege are the hospitals using remdesivir without informed consent, leading to wrongful death.
The lawsuit addressed what the attorneys called “the remdesivir protocol,” in which the patients may be admitted to the hospital—often for problems unrelated to COVID-19—and then diagnosed with COVID-19 or COVID pneumonia.
The patients are then isolated and malnourished before being told remdesivir is their only treatment option, according to the lawsuit.
The patients are also placed on a BiPap machine, which uses pressure to push oxygen into the lungs at a high rate, the lawsuit says, with the patients’ hands often tied down so they can’t remove it.
The final stage of the protocol is intubation, at which point the patients die an average of nine days after being admitted, the lawsuit states.
In the end, the hospital can get up to $500,000 in reimbursement per patient for the protocol.
‘Things Just Got Worse’
Seiler goes into more detail about her story on the FormerFedsGroup Freedom Foundation’s COVID-19 Humanity Betrayal Memory Project.
She became the Texas chairperson for the foundation, where she gathers stories similar to hers to submit to the project’s documented cases.
The foundation also offers multiple online support group meetings where others can tell their stories.
The number of people who say they’ve had family members die in hospitals at the hands of what they call the “death protocols” continues to surface. However, for many of them, their loved ones’ deaths left them with inconceivable stories of administrative cruelty.
Patients and families are scared into accepting treatment such as remdesivir without being informed about the risks such as kidney failure.
Families have reported that physicians will tell them that the patient needs oxygen and rest, then the oxygen is used to such a high degree that later a ventilator is required because the lungs are damaged.
When a patient tries to remove the BiPap mask, they are deemed agitated and given sedatives, leaving them at the mercy of hospital staff, many reported, while being denied access to basic nutrition, hygiene, and exercise.
For Seiler, the lack of nutrition caused hair loss, and she developed a bacterial infection called thrush because no one removed her BiPap mask to clean her mouth, she said.
Seiler said the doctors and nurses wouldn’t allow her to even sit up, resulting in bed sores, and she eventually lost her ability to walk.
After two days on a catheter that she said was forced on her because nurses told her they couldn’t take her to the bathroom, she got another infection from the catheter.
“Things just got worse,” Seiler said. “People were dying around me in other rooms. Quite frankly, it was quite scary, and I knew that time was short.”
‘I’m Going to Take You Out of There’
On Dec. 14, 2021, Seiler’s husband, a former nurse and U.S. Army veteran, called 911 to have the Plano Police Department perform a welfare check, she said.
When the police officer arrived, Seiler said she attempted to explain to him what she had experienced.
“I told him they’re going to murder me,” she said. “He said, ‘We don’t have a protocol for this,’ and he left.”
Having exhausted all other options, Brad Seiler and Seiler’s daughter—who had been contacting politicians for help—came up with a plan to get her out of the hospital and take her home.
Brad Seiler set up oxygen and obtained medications with the help of a home consultation service and Dr. Richard Bartlett’s protocols, which emphasize the use of budesonide, she said.
On Dec. 15, Brad called and told her, “I’m going to take you out of there.”
Brad arrived with a cease-and-desist letter and two pieces of patients’ rights legislation, written to allow access to at least one visitor: Texas Senate Bill 572 and Senate Bill 2211.
The state’s House and Senate bills prohibit hospitals from denying visitation, including clergy visitation, during disasters such as the COVID-19 pandemic.
Seiler said Quach found a loophole in the House bill where it says the doctor can write an order for five days limiting visitation to one person, and then renew that order.
“And that’s what Dr. Quach had done to keep me isolated,” she said. “Still, Quach broke the premise of that bill, because I wasn’t allowed any visitors.”
The Senate bill, which was written by state Sen. Bob Hall, permits a spiritual counselor, she said.
This was written to include family members, which is why Brad was brandishing the legislation—to invoke himself as the spiritual head of the family, Seiler said.
‘I Anticipate There Will be Future Hearings’
Hall, who was involved in making calls to the hospital to petition for Seiler’s care, has been outspoken against “the commandeering of medical practices by the government.”
In June 2022, the Texas Senate Committee on Health and Human Services held a hearing where families testified about their loved ones’ experiences with the medical system during the pandemic.
In a statement to The Epoch Times, Hall said he anticipates future hearings after the committee heard the personal testimonies.
“Patients and doctors must be empowered to make decisions on treatment protocols without fear of threats and intimidation if they differ from government-mandated procedures,” Hall said.
It was the persistence of Seiler’s husband and daughter, Hall said, that made Seiler “one of the few hospital COVID patients to get out of the hospital in time to survive.”
Echoing Seiler’s earlier statement, Hall said “more people died in hospitals like Medical City Plano because of hospital policies, than died of COVID.”
In a statement to The Epoch Times, a Medical City Plano spokesperson said that “like other hospitals in our area, our hospital relies on licensed, independent physicians who use their extensive training and experience to assess patients’ needs and determine the course of treatment. We support our physicians by giving them information and resources, including the latest research to help them provide the best possible care to our patients.”
Of the many consequences of the COVID-19 pandemic, the erosion of confidence in the medical profession’s “best possible care” has been the most damaging, Hall said.
“The circumstances triggered a number of egregious policies and practices never before seen in our modern hospitals,” Hall said. “Patients were isolated from their families and loved ones, intimidated or coerced into receiving medical protocols with which they disagreed, and in some cases, outright neglected. Government-mandated protocols, which did more harm than good, added fuel and distrust to the fire.”
‘I Know for Certain I Will Die at Your Hands’
Brad Seiler had gone beyond the stage of distrust when he entered the hospital and somehow charged his way into the ICU as security chased him, Gail Seiler said.
When told to leave, Brad told staff, “You’re not going to murder my wife. She’s coming home with me,” Seiler said.
From there, it became almost like an all-day hostage negotiation, Seiler said, with six police officers who were there not to help them, but to make Brad leave.
Hall got involved, telling Brad not to resist if officers were to arrest him, Seiler said, while one of the doctors told her that if she were to leave with Brad, she would die.
“I told her that if I died tonight, ‘I’d prefer it be with Brad trying to save me rather than die at your hands because I know for certain I will die at your hands,’” Seiler said.
Seiler needed a wheelchair because her legs didn’t work due to a lack of physical therapy, she said.
When she was packed and ready to leave, Seiler said the floor nurse led them out through what he called “the shortcut,” which turned out to be the way through the morgue where the funeral homes pick up bodies.
“I think it was to send us a message,” Seiler said.
‘A Medical Matrix’
Despite the physician telling Brad Seiler that his wife wouldn’t make it 24 hours if she left the hospital, she lives today to tell her story.
It wasn’t easy, Gail Seiler said, and her healing at home had more to do with recovering from her experience at the hospital than from the virus itself.
However, it was Bartlett’s treatment that saved her life, she said.
“Everything he put in place works,” she said. “I started to improve right away.”
The Seilers later contacted their state representative who contacted Health and Human Services (HHS) to conduct an investigation, Gail said.
HHS assigned the investigation to the hospital, which concluded that the hospital had “done a stellar job,” Gail said.
“No one contacted us, and they certainly didn’t look at our medical records because—if anything—even making someone a DNR when they tell you they aren’t a DNR is against the law, right?” Sieler said.
The Seilers were sure no one would believe their story, but as they continued to tell it on podcast and radio interviews, more and more people contacted them to share their own experiences.
Seiler managed to escape the hospital and recover, but she said most of the stories she hears from other people don’t have happy endings, leaving those families wracked with guilt when they realize what took place.
The majority of the cases have ended in the death of the patient, Seiler said, with the family only realizing they had been gaslit after it was over.
“What we’re seeing is doctors aren’t being honest with the patient, and by the time you realize they’re harming you, you’ve not only been harmed, you’ve also been gaslit, and you can’t just leave,” Seiler said. “You’re on a high flow of oxygen and you’re told if you leave, you’ll die. If you get intubated, the only way out is to be transferred to another hospital.”
Patients have generally had the right to advocate for their own medical treatment, and even deny recommendations, but with the emergency declarations related to COVID, hospital staff have been given authority over patients they’ve historically not had, Seiler said.
In some cases, patients have been given remdesivir and other medications not only without informed consent but also after the patient had put in writing that they didn’t want the drug, Seiler said.
Despite this overreach being exercised in hospitals, Brad and the Seiler’s daughter was able to bring enough attention to the case through networking with Hall and Lt. Col. Allen West, Seiler said.
West had also been treated there and—in addition to Hall—made several calls to the hospital on the Seilers’ behalf, which Seiler said she suspects is why staff had to eventually acquiesce to letting Brad remove her.
There have been cases in which people have just walked out, but they are rare, Seiler said.
“Once you enter the hospital, you’re in this medical matrix, and the only way out is through death or if someone comes and takes you out,” Seiler said.
Today, Seiler’s mission is to bring awareness by sharing her story and the stories of others, she said.
“My goal is to keep people out of hospitals because this truly is a hospital holocaust.”
EXCLUSIVE: FDA Refuses to Provide Key COVID-19 Vaccine Safety Analyses
By Zachary Stieber
September 10, 2022Updated: 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.
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.”
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.
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.
More Reports of COVID Vaccine-Linked Heart Inflammation in Young Males Submitted to CDC
By Jack Phillips September 11, 2022Updated: 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.
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.
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.
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.
“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?”
Are you growing weary of the world wide global plandemic? Many are wondering why is all this happening. We have been programmed since birth by Tel-A-Vison . We told how to think by educators, politicians and religious leaders. We trusted the medical and pharmaceutical industries, that are making us sick. We trusted the media to tell the truth. It is the World Economic Forum plan to control the masses.
So you may ask what can I do, I am just one person. One persons thoughts, emotions and actions generates energy. We are all connected to each other and our Creator. We are being tested. Free will, the right to choose, how we live, and how we treat others are all part of the test. Do we live to serve ourselves or do we live to serve others, a negative or positive path? Do we love unconditional or do we live in fear? Do we even know what love means? What happens if we don’t learn? So many unanswered questions throughout the ages.
Sacred texts such as the Bible, Vedas, Quran, Tanakh, just to name a few, provide their Translations, interpretations and explanations through other men for centuries Man is probably more confused today than ever before. Religions seem to take us so far based on the information but we have to use our gift of discernment. Seek the truth and it will set you free.
Consider there was no difference between right and wrong, which is positive and negative energy. The idea is to get at least 51 percent positive in order to advance spiritually, not just in this life time, but all your life times. It is more difficult to go down the negative path which requires 95 percent negative. You keep reincarnating until you get the passing grade.
We are all blessed to be on earth at this time to experience the greatest spiritual awakening in earth history. The Axial Age, occurred during the 8th to the 3rd century BCE was , the evolution of human thought. Religious and philosophical activity took place in Asia and the Mediterranean. During this time, Jeremiah, Isaiah, The Buddha, Confucius, Vardhamana Mahavira, Pythagoras, Heraclitus, Socrates, Plato and Aristotle, produced the intellectual and moral matrix out of which the world religions were born. Religion developments are based in the ideas, concepts and insights from the Axial period.
Now we are part of a new age and we can positively change our world. We have to do it together with compassion and love, Seek the truth
The video below provides updates regarding what is happening around the world. Use your discernment.
The signs we receive from our spirit guides will be unique to each person and now more than ever, it is time to pay attention. It is important to recognize the polarity, positive and negative entities providing messages. The key is to pay attention. For those who are seeking the truth the signs may be more noticeable. Common signs would be dreams and numerology.
I had two dreams I will share with you that I considered negative. I have been seeking the truth for quite some time. For two nights in a row, I had the same dream, it was a tune that sounded faintly familiar, but no lyrics. It was driving me crazy so I started listening to songs and two days later finally found it, Lonesome Loser.
Another dream was a woman wrapped up like a mummy, limping and walked to me and said, this is what love does to you. Both dreams were talking about love and how it hurts.
Numerology is a common sign, 111, 222, etc., are considered wake up calls. It is a language of its own and eventually, if you pay attention, you begin to understand.
Nature is a big thing for me. An Eagle flying over and a white dove sitting on my house which I have never seen before. Owls and hawks being more active during some of my thoughts. While in the garden, contemplating and wondering if I am on right track, I would see a dragonfly until I had my answer and then it would disappear. Tones in the left or right ears during my thoughts occur often. Again, these are just some of my signs that I have experienced.
Our thoughts create our emotions that may result in action. That is why it is important to have love and compassion in your heart and a little wisdom does not hurt. Our guides are just trying to keep us straight during our life journey. Discernment will help you to determine the polarity of the signs you receive. Pay attention and you will realize the world is not as it seems. The videos below may help with that understanding.
World Economic Forum’s ENTIRE plan EXPOSED in just 60 seconds.
Telling it like it is
Deagel, an intelligence organization for the US government, predicts a massive 50-80% global depopulation by 2025. Despite the overwhelming removal of its significance, WikiLeaks documents revealed that Deagel was legitimately used as a reference material in a Stratfor report on the technological capabilities of the North Korea.
United States – 327 million => 100 million
France – 67 million => 39 million
England – 66 million => 15 million
Australia – 23 million => 15 million
Germany – 81 million => 28 million
Canada – 36 million => to 26 million
Projections were made in 2017. To make matters even stranger, a statement on Deagel’s predictions page apparently claims that a large portion of the population movements are due to suicide. These predictions feels more and more real every don’t they?
Whistleblower Lawyer: FBI Agents Have Lost Confidence in Director Wray
By Jack Phillips
August 31, 2022Updated: August 31, 2022
A lawyer representing several unnamed FBI whistleblowers said Wednesday that agents have lost confidence in the bureau’s leadership amid recent controversy.
The FBI and the Department of Justice (DOJ) have faced Republican criticism over the raid of former President Donald Trump’s Mar-a-Lago, while a number of whistleblowers have provided testimony to GOP lawmakers about alleged political bias at the bureau. Over the past weekend, high-ranking FBI agent Timothy Thibault departed the agency amid whistleblower complaints.
“I’m hearing from [FBI personnel] that they feel like the director has lost control of the bureau,” Kurt Siuzdak, a lawyer and former agent who represents FBI whistleblowers, told the Washington Times on Wednesday. “They’re saying, ‘How does this guy survive? He’s leaving. He’s got to leave.’”
Siuzdak told the paper that FBI agents have told him they’ve “lost confidence” in FBI Director Christopher Wray. “All Wray does is go in and say we need more training and we’re doing stuff about it, or we will not tolerate it.”
In March, Siuzdak told the New York Post that he left the FBI after a 25-year career as an agent due to what he says is a lack of accountability among FBI managers and the bureau’s leadership. He blamed it on political biases held by top managers and leaders.
Whistleblowers, Siuzdak told the paper this week, have alleged that Wray didn’t take action on a variety of matters, including sexual harassment claims and agents being forced to sign fake affidavits. Trump nominated Wray in 2017 after firing former Director James Comey.
When contacted by The Epoch Times last week about recent whistleblower claims, the FBI issued a statement that the “men and women of the FBI do their jobs with rigor, objectivity, and a fierce commitment to our mission.”
“All FBI employees are held to the highest standards of professional and ethical conduct. Allegations of misconduct are taken seriously and referred to the Inspection Division or the Department of Justice Office of the Inspector General. Through the disciplinary process, the FBI will continue to hold employees accountable for any substantiated misconduct,” the agency added.
The FBI on Wednesday appeared to send the same statement to the Washington Times about Siuzdak’s interview. The Epoch Times has contacted the agency for additional comment.
Last week, Rep. Matt Gaetz (R-Fla.) said he’s received new whistleblower complaints from FBI employees, calling for a new investigation.
“The guy told me that he loves the bureau, that he doesn’t want to see the bureau defunded or destroyed, but that he really feels a need to come forward so that there’s a focus on the things they ought to be doing, not trying to affect political outcomes,” the GOP lawmaker said.
As for Thibault, a lawyer representing the former FBI agent told news outlets that he left the agency on his own terms and it had nothing to do with Hunter Biden or Trump. Whistleblowers have alleged to Sen. Chuck Grassley (R-Iowa) that Thibault slow-walked the Biden laptop investigation and expressed animus toward Trump, according to letters he’s sent to FBI leaders.
“In the last couple of months, and particularly the last 24 hours,” a lawyer for Thibault said Tuesday, “there have been a number of inaccurate media stories and allegations on social media about our client.”
The lawyer said Thibault did not supervise the investigation into Hunter Biden. And neither did Thibault display any political biases in his work, the lawyer added, reported Time magazine.
“In particular, Mr. Thibault was not involved in any decisions related to any laptop that may be at issue in that investigation, and he did not seek to close the investigation,” the lawyer said, adding that he wasn’t involved in the Mar-a-Lago raid either.
We always depended on our medical communities to help us heal, however in todays world, that is changing. As we learn of the criminal acts many medical professionals and hospitals have committed in the last two years over covid, it is time to change our thinking.
We are energetic beings with the ability to heal ourselves once we are able to tap in to our divine source, energy that is available to all. Being aware of our true nature and the general science of the nature of disease and it’s cure is a great start. Our intention with the understanding of our true nature will increase healing energy that will begin to flow through our body energy centers. Then we may be able to heal ourselves, and then perhaps even assist others.
A good example is Dr Joe Dispenza, who healed himself after breaking 6 vertebrae in his back after being told he would never walk again. Through meditation, visualizations and his belief system, after nine and a half weeks after the accident, he got up and walked, without having any body cast or any surgeries.
We are subject to three types of diseases that affect our body, mind and Spirit and the are are interrelated. Our spirit is haunted by the disease of ignorance born of cosmic delusion which cause man to forget their perfect divine nature and focus on the physical world. Ignorance creates imbalances between body, mind and spirit. Then disease normally occurs during recurring negative thoughts, emotions and actions. We all know he law of Karma, we reap what we sow.
Our every expression through our thoughts, emotion and actions holds a specific frequency which influences everything around us. Carrying certain emotions in our hearts and minds shows that we are literally carrying those shapes in our bodies. By keeping our minds positive with love and compassion, the flow of energy will follow.
We all have the ability to heal ourselves, with will and desire. It starts with our thoughts, emotions and actions. Our diet plays a key role in keeping our body heathy and strong. It is our temple and we should treat it as such. When we discover our true nature the energy healing of the spirit begins. When we open our eye of wisdom by meditation, contemplation and prayer, the physical and mental agonies are dispelled by the love and light of our source, God by many names. The more we spiritually awaken, our possibilities are limitless including channeling the energy for healing .
5G Led Street Lights have crippled runner beans.
Mark Steel interview about 5G. More and more experts come out into the open to tell the truth. There are ways to stop the EMF radiation coming from all electronical devices. Learn more here: https://dq271.isrefer.com/go/AultHome/AUL651/
Did you noticed we never had any skin cancer issues until they rolled out this toxic sunscreen product and lied to everyone about the sun and the ozone layer?
People unwittingly put these toxins in their bodies thinking they are protecting themselves, while in reality all they were doing was poisonings their system.
A sure way to avoid this deceptive trap is knowing that whatever is pumped and promoted in mass consciousness. You can bet that it’s a lie, and it will have the opposite intended effect of harming you.
They have used this strategy for these products: