Deep Fake; Judge in NYC Declares Vaccine Mandates Unconstitutional; The Concerning Rise of GMO Food Animals

Deep Fake

This is how we are being conned by CGI deep fakes… This is a must watch.


Judge in NYC Declares Vaccine Mandates Unconstitutional, Says Shots Don’t Prevent Infection or Spread

A state Supreme Court ruling in Richmond County, New York, has declared that the vaccine mandates were unconstitutional and in violation of the separation of powers. The determination includes all public workers in the city, including in the police and fire departments. The decision gives legal grounding for additional lawsuits throughout the country, and could impact attempts at future vaccine mandates.


  20 Million Death


UK Column News: Patrick Henningsen on collusion between Pfizer and the CDC the shift their increasingly unpopular COVID vaccine products, as CNN and NY Health Dept begin pushing to Polio scare.


A quiet effort is underway to maximize profits by manipulating the genes of food animals

Jun 30 2022

The health conscious and safe food advocates are well aware of genetically modified organisms (GMO) such as the corn that Monsanto designed to withstand heavier exposures to its juggernaut herbicide Roundup.

Less publicized, however, are GMO food animals. Judging from ongoing research, the companies making these creatures hope they will increasingly find their way onto Americans’ plates in the years ahead. The AquAdvantage salmon was approved by the U.S. Food and Drug Administration (FDA) in 2015, but other GMO animals are under development.

The AquAdvantage salmon was created by inserting the coding sequence from a Chinook salmon growth-hormone gene under the control of an “antifreeze protein promoter and terminator” from the eel-like ocean pout into wild Atlantic salmon.

Designed to grow twice as fast as normal salmon, it was the first GMO animal approved by the FDA. According to a food industry website, the Counter, the AquAdvantage salmon is sold in Canada, but more than 85 grocery chains, food service companies, restaurants, and seafood companies have pledged to boycott it for both food safety and environmental reasons.

In addition to concerns about the product itself, the safety of wild salmon populations is threatened by such GMO animals if they escape. (Think Jurassic Park.)

While both the FDA and the AquAdvantage (AAS) salmon’s creator, AquaBounty, claim the GMO salmon is safe to eat, the FDA briefing packet disseminated for 2010 hearings revealed such red flags as a higher incidence of “jaw erosion” and “focal inflammation” (infection) seen in the AAS salmon; no way to determine if greater allergy risks existed because of the excessive culling of “abnormal” AAS salmon; and a possible “increase in the level of IGF-1,” insulin-like growth factor-1, in the AAS salmon.

Moreover, FDA food scientists and outside experts who had been called in for the hearings noted unexplained discrepancies, omitted data, and overall substandard science presented by those promoting the AAS salmon.

More FDA GMO Approvals

In 2020, the FDA approved the second GMO animal, an “intentional genomic alteration” (IGA) in pigs. The lab-created animal, called a “GalSafe” pig, is designed to eliminate a substance found on the surface of pigs’ cells called “alpha-gal sugar” that could cause people with alpha-gal (AGS) syndrome to have an allergic reaction. AGS sensitizes someone to allergic reactions to beef, pork, and lamb usually after a tick bite. The GMO animal was created by removing the gene for alpha-1, 3-galactosyltransferase, which “attaches alpha-galactose sugars to cell surfaces,” Medpage Today reported.

GMO animals are already used in the laboratory. In the 1980s, transgenic mice were created by inserting human genes and a sheep with human genes was created in 1997. GMO animals are also used in medical and non-food applications. In 2009, the FDA approved an anti-clotting drug made from goats that had the human gene for antithrombin inserted and linked to their DNA.

More Livestock Genetic Engineering

In 2006, research published in the journal Nature Biotechnology describes the “generation of cloned pigs that express a humanized Caenorhabditis elegans gene, fat-1, encoding an n-3 fatty acid desaturase,” in order to produce pork with more “good” omega-3 fatty acids and less “bad” omega-6 fatty acids that are usually found in meat.

In 2010, researchers created a GMO pig by adding mouse and E. coli phytase genes to its DNA, and the creature was approved in Canada. Dubbed the “Enviropig,” it was said to produce less phosphorus in its urine and feces and be less destructive to the environment but the pigs were killed in 2012 when funding ran out.

In addition to creating animals that are more environmentally friendly or that have better nutritional profiles for human consumption, in 2007, United Kingdom scientists at the Roslin Institute, near Edinburgh, announced that they had produced genetically modified chickens to lay eggs that contain cancer-fighting drugs according to the BBC.

“Some of the birds have been engineered to lay eggs that contain miR24, a type of antibody with potential for treating malignant melanoma, a form of skin cancer. Others produce human interferon b-1a, which can be used to stop viruses replicating in cells,” the news agency reported.

“Once you’ve made the transgenic birds, then it’s very easy; once you’ve got the gene in, then you can breed up hundreds of birds from one cockerel—because they can be bred with hundreds of hens and you can collect an egg a day and have hundreds of chicks in no time,” said Dr. Helen Sang, lead scientist on the project.

Overseas GMO Animals

In 2011, scientists at the China Agricultural University introduced human genes into dairy cows to produce milk closer in composition to that of humans. They hoped the milk from GMO cows would be sold in supermarkets and positioned it as an alternative to formula and human breast milk for babies. Soon after, scientists in Argentina also created a cow with human genes to approximate human breast milk, and scientists from New Zealand added a mouse gene to a cow to produce allergy-free milk.

When the human/cow GMO animals were announced, Helen Wallace, executive director of the biotechnology monitoring group GeneWatch UK, told the Telegraph: “We have major concerns about this research to genetically modify cows with human genes.

“There are major welfare issues with genetically modified animals as you get high numbers of stillbirths.” Wallace also questioned whether the milk “could be harmful to some people” with no large clinical trials having been conducted.

Others question the morality of adding human characteristics to animals.

More GMO Animals Likely to Come Before FDA

So far, the AquAdvantage salmon, the “GalSafe” pig, and the GMO goat have been FDA approved, and genetic engineering of food animals looks set to ramp up as meat producers seek to maximize profits and modify animals to crowded growing conditions, consumer appetites, and marketing possibilities.

“Genome editing has been found to be a valuable tool for lightening the hair and coat color to better adapt dairy cattle to rapidly changing climatic conditions,” Giuseppe Ambrosi, European Dairy Association president, told Dairy Global. “These are the findings by researchers from the AgResearch Centre in New Zealand. High-producing Holstein Friesian dairy cattle have a characteristic black and white coat, often with large proportions of black. Compared to a light coat color, black absorbs more solar radiation.”

Earlier this year, National Hog Farmer wrote that genetic engineering “has the potential to transform how we improve livestock with genetics … increasing agricultural productivity (more food for more people in our community and elsewhere). While the article hints that genetic engineering could cut down on antibiotic usage, many operations are already using vaccines to that end.

GMO dairy cattle have been developed to grow without horns by taking DNA from the genome of Red Angus cattle, which suppresses horn growth, and inserting it into the cells of a Holstein bull. Pigs resistant to porcine reproductive and respiratory syndrome (PRRS) have been genetically engineered and researchers have been trying to genetically engineer cows that are immune to the terminal, prion-caused disease known as “mad cow” after the worldwide outbreaks in the early 2000s.

While stopping disease is a worthy goal, many animal diseases—like the current avian influenza epidemic—are caused or worsened by crowding and unsanitary conditions.

Conclusion

The development of genetically engineered food animals will likely increase because the GMOs represent greater profits for big meat producers when they adjust animals to their bottom line rather than their practices to better suit animal welfare and human safety.

However, like GMO crops, many environmental and food groups distrust the products (sometimes called “Frankenfoods”) and raise legitimate questions about their safety, purpose, and who is driving the aggressive GMO agenda.

Moreover, the objections to GMO crops—tampering with nature for human advantage—are magnified when it comes to animals.

Creating new animals for a dedicated human use “is a mechanistic use of animals that seems to perpetuate the notion of their being merely tools for human use rather than sentient creatures,” the Humane Society of the United States says. That may be an understatement.

Martha Rosenberg

Martha Rosenberg is a nationally recognized reporter and author whose work has been cited by the Mayo Clinic Proceedings, Public Library of Science Biology, and National Geographic. Rosenberg’s FDA expose, ‘Born with a Junk Food Deficiency,’ established her as a prominent investigative journalist. She has lectured widely at universities throughout the United States and resides in Chicago.

Murder by Vaccines; More Than Halve Children had Systemic Reactions to Jab; Judge Grants Trump Motion for Special Master;

Murder by Vaccines Documentary

In CDC Survey of Over 13,000 Children, More Than Half Had ‘Systemic Reaction’ After COVID-19 Vaccine

Parents reported 6 percent of young children were unable to do normal activities after second dose
By Margaret Menge
September 4, 2022 Updated: September 4, 2022

In a CDC survey of over 13,000 children, more than 55 percent of the subjects between the ages of 6 months and two years had a “systemic reaction” in response to their first dose of the Pfizer-BioNTech or Moderna COVID-19 vaccines, the CDC said on Sept. 1.

A systemic reaction is a response beyond the injection site. The CDC said almost 60 percent had a systemic reaction to the second dose of the Moderna vaccine.

While the most common systemic reactions were fatigue, fever, irritability, and crying, parents of more than 6 percent of the children in the study said their child was unable to perform normal activities after the second dose of either the Pfizer-BioNTech or Moderna vaccine.

The CDC collected the data through a program called V-Safe—a smartphone-based monitoring system that operates through an app that parents download to their phones.

Between June 18 and Aug. 21, parents of more than 10,000 young children reported reactions to the CDC through V-Safe in the seven days after their child received a COVID-19 vaccination.

Parents of 8,338 children ages six months to 2 years who received the Moderna vaccine reported information through V-Safe, with 55.7 percent reporting a systemic reaction after the first dose and about 58 percent after the second dose. For the Pfizer vaccine, parents of 4,749 children ages six months to 2 years submitted reports showing that 55.8 percent had a systemic reaction after the first dose and about 47 percent after the second dose of the vaccine.

Epoch Times Photo

The most frequently reported reactions for children six months to 2 years were irritability or crying, sleepiness, and fever. The most common reactions for children aged 3-5 years were injection site pain, fatigue, and fever.

Epoch Times Photo

Health Impacts

The data also showed a more serious reaction category labeled “any health impact.”

About 10 percent of all children six months to 2 years were reported to have a “health impact” after getting their first dose of either the Moderna or Pfizer vaccine. For the Moderna vaccine, slightly more children had a health impact after the second dose; for the Pfizer vaccine, it was slightly less.

The information was presented to the CDC’s Advisory Committee on Immunization Practices (ACIP) on Sept. 1 as part of an overview of all data related to the safety of COVID-19 vaccines.

In addition to V-Safe, data was presented summarizing reports from the Vaccine Adverse Event Reporting System (VAERS) and the Vaccine Safety Data Link (VSD), which includes data from several large health maintenance organizations in the United States.

All three systems look at the safety of vaccines after they’ve already gone to market and have been administered to large numbers of people.

Tom Shimabukuro, the head of the CDC’s vaccine safety team, headed the presentation and told committee members that no “statistical signals” of COVID-19 vaccine reactions were found for young children in the VSD data.

Shimabukuro also said that systemic reactions were “commonly reported” following vaccines.

However, other medical professionals like Dr. Meryl Nass from Children’s Health Defense have expressed caution over the reported reactions, pointing to the high number of systemic reaction reports among very young children.

She told The Epoch Times on Sept. 2 that she was questioning why the government doesn’t collect and present more information on these cases.

“That stuff is not considered by the CDC to be very important … It’s assumed that all those side effects go away after a few days and leave the people perfectly well,” she said, mentioning the fevers and fatigue. “Those reactions may in fact may be harbingers of more serious reactions, but nobody to my knowledge has published anything looking at whether these acute local or systemic reactions are indicators of a later problem.”

The FDA approved the emergency-use authorization of COVID-19 vaccines for children aged six months to 5 years on June 17. According to the CDC, about 599,460 children in this age group have received the Pfizer-BioNTech vaccine, and about 440,770 have received the Moderna vaccine.

From June 18 through Aug. 31, approximately 1 million doses of the Moderna and Pfizer vaccines were administered to children in this age group.

In a review of the VAERS data on young children from June 18 to Aug. 31, the CDC had 496 reports of adverse events for children aged six months to 4 years who received the Pfizer vaccine and 521 for children aged six months to 5 years who received the Moderna shot, with an adverse event defined as a possible side effect.

Over 98 percent of reports were for what the CDC considers non-serious events.

There are 220 reports of persons aged six months to 5 years of age being taken to the emergency room following a COVID-19 vaccine. In one case involving a 2-year-old boy in Arizona, the VAERS report says he was given the Pfizer vaccine on July 29 and on July 30 had a “life threatening episode.”

The report lists his symptoms as “clammy skin and vomiting leading (8 minutes) to difficulty breathing.” The boy “turned blue,” was “limp” and “non-responsive,” and “fully stopped breathing for two minutes,” according to the report.

He was revived after chest compressions.


Never Forget What They Did

 

Judge Grants Trump Motion for Special Master to Review Records FBI Seized

By Zachary Stieber
September 5, 2022 Updated: September 5, 2022

A U.S. judge on Sept. 5 agreed to insert a special master into the review process for records seized from former President Donald Trump’s home.

U.S. District Judge Aileen Cannon, a Trump appointee, ordered the appointment of a special master to review the seized property for items and documents that may be covered by attorney-client and/or executive privilege.

“In addition to being deprived of potentially significant personal documents, which alone creates a real harm, Plaintiff faces an unquantifiable potential harm by way of improper disclosure of sensitive information to the public,” Cannon wrote in her 24-page order, released several days after a hearing in which she heard arguments from Trump’s lawyers and attorneys for the government.

“Further, Plaintiff is at risk of suffering injury from the Government’s retention and potential use of privileged materials in the course of a process that, thus far, has been closed off to Plaintiff and that has raised at least some concerns as to its efficacy, even if inadvertently so,” she added.

A special master is an independent third party who assists with sensitive cases.

Cannon did not yet name a specific person to be the special master.

FBI agents seized records, notes, and other items from Trump’s resort in Palm Beach, Florida, on Aug. 8.

Cannon said she was swayed to side with Trump in part because the U.S. government’s filter team, which was supposed to identify all potentially privileged items, failed to do so.

“Those instances alone, even if entirely inadvertent, yield questions about the adequacy of the filter review process,” the judge said.

Executive Privilege

U.S. Department of Justice (DOJ) officials have maintained that Trump cannot legitimately exert executive privilege claims because he is no longer in office, pointing to a determination by the acting U.S. archivist, but Cannon said she didn’t necessarily agree.

“In the Court’s estimation, this position arguably overstates the law,” she said.

In the U.S. Supreme Court’s decision in Nixon v. Administrator of General Services, cited by acting Archivist Debra Wall and DOJ lawyers, a majority of the court found that a new law governing the custody of presidential records did not violate the U.S. Constitution or executive privilege.

But the court also “did not rule out the possibility of a former President overcoming an incumbent President on executive privilege matters,” Cannon said.

“Further, just this year, the Supreme Court noted that, at least in connection with a congressional investigation, ‘[t]he questions whether and in what circumstances a former President may obtain a court order preventing disclosure of privileged records from his tenure in office, in the face of a determination by the incumbent President to waive the privilege, are unprecedented and raise serious and substantial concerns,’” she added, citing a decision in Trump v. Thompson.

Even if Trump’s assertion of executive privilege ultimately fails, former presidents can still raise the possibility “as an initial matter,” making the filter team’s failure to screen for material potentially falling under the assertion another reason to appoint a special master, according to the judge.

US-POLITICS-INVESTIGATION-TRUMP
A local law enforcement officer in front of the home of former President Donald Trump at Mar-A-Lago in Palm Beach, Fla., on Aug. 9, 2022. (Giorgio Viera/AFP via Getty Images)

List of Proposed Candidates

Trump’s lawyers and U.S. lawyers were directed to confer and submit a joint filing that includes a list of special master candidates.

The filing shall also include proposals for how the special master should operate, Cannon said.

Any points of major disagreement should be identified in the joint filing.

An outside party recently submitted a list of four proposed candidates to the court, including at least one academic who has a history of animus against Trump.

“The United States is examining the opinion and will consider appropriate next steps in the ongoing litigation,” a spokesperson for the DOJ told news outlets after the ruling was issued.

Pause

Cannon also reserved ruling on Trump’s request for return of property and ordered the government to stop reviewing and using the seized materials for its ongoing investigation into Trump.

Officials allege evidence indicates Trump violated several laws, including one barring certain handling of defense information.

U.S. intelligence officials, though, are being allowed to continue their review of potential damage from Trump holding records marked classified.

Zachary Stieber

REPORTER

Pfizer Twisted Their Clinical Trial Data for Young Children; Crimes Against Humanity; It’s Genocide

Dr. Clare Craig Exposes How Pfizer Twisted Their Clinical Trial Data for Young Children

Crimes Against Humanity | Part 2

 

‘It’s Genocide’: Family Alleges Ominous Conclusion in Seeking Answers to Their Daughter’s Death

By Matt McGregor
June 19, 2022 Updated: June 19, 2022

Eight months after his 19-year-old daughter Grace died in a hospital after having been given a combination of a sedative, an anxiety medication, and morphine, Scott Schara and his family continue to bring attention to why they think she died, and who’s responsible.

Their most recent billboard campaign targets St. Elizabeth’s Hospital in Appleton, Wisconsin, where his daughter with Down’s syndrome passed.

Hospital staff driving to and from work would have a hard time not seeing the billboards that ask, “Was Grace given a lethal combination of meds at St. Elizabeth’s Hospital? Intentional? … Who’s Next?”

Others ask, “Was Grace labeled Do Not Resuscitate without family consent at St. E’s?”

Grace died in October 2021, a month after COVID-19 vaccine mandates had been announced by President Joe Biden.

People who didn’t want to take the experimental vaccine were being fired, while unvaccinated patients in hospitals were being treated much differently than the vaccinated.

Reports from people such as Anne Quiner in Minnesota painted a picture of medical discrimination and unusual hospital protocols that many, like Quiner, alleged led to the death of their loved ones.

According to Schara, Grace, who, like the rest of her family, was unvaccinated, was admitted to St. Elizabeth’s for COVID-19 respiratory issues on Oct. 6 but had been recovering when the doctor began giving her a sedative called Precedex.

Schara said there were frequent incidents of discrimination regarding Grace’s unvaccinated status, and their choice to use other early treatment medications that weren’t approved by Dr. Anthony Fauci, the director of the National Institute of Allergy and Infectious Diseases.

Grace was on Precedex for four days preceding her last day, Schara told The Epoch Times, despite severe risks associated with being on the drug for longer than 24 hours.

On Oct. 13, the day Grace died, she was given—in addition to the Precedex—Lorazepam, and morphine within a 29-minute window, Schara said, even though the package insert for morphine warns against using it in combination with the other two drugs because it can result in death.

With an armed guard standing near the doorway of her room at the hospital, Schara said Grace’s sister and patient advocate begged nurses she saw in the hallway to revive Grace as their parents watched from Facetime, joining her in their pleas.

There was nothing to be done, a nurse responded because Grace had been coded as Do Not Resuscitate (DNR), a label that Scott said must be legally approved and signed off on by the medical power of attorney, who was Grace’s mother, Cindy.

The family said this never happened.

“Why would we agree to a DNR when we would not only want the doctors to save our daughter at any cost but also the morning of Grace’s last day, the doctor recommended a feeding tube to start the process of getting Grace home?” he asked.

The doctor had told the family, Schara said, that Grace “had a good day yesterday; we should work on nutrition,” before recommending a feeding tube.

Medical records seen by The Epoch Times show that the DNR order was put into the system eight minutes after a maximum dose of Precedex was administered at 10:48 a.m., on Grace’s last day, which Schara calls the “smoking gun.”

“She had been on Precedex for four days at this point, then they gave her close to the maximum dose,” he said. “Eight minutes later, the doctor puts the illegal DNR on her.”

According to her death certificate, Grace died of acute respiratory failure with hypoxemia.

Schara said “respiratory failure” is a direct side effect of using Precedex for more than 24 hours.

“Of course, COVID-19 pneumonia is listed as the second cause of death in order for the hospital to receive the killing bonus from the government,” he said.

Epoch Times Photo
The Schara family’s billboard campaign, 2022. (Courtesy of Scott Schara)

‘We Are in a Spiritual Battle’

Since then, Schara said he has continued investigating and has found even more negligence.

To bring attention to what happened, he’s been on over 100 media outlets, and has even held a rally with city approval outside of the hospital, he said.

Schara said the family has committed over $300,000 to the campaigns, $225,454 of that is for the billboards they put up through May 2023.

“Money is temporary,” Schara said. “I don’t want this to happen to anyone else. We are in a spiritual battle, and people must realize that.”

After telling his story to a wider audience, Robin Riley from Newtown, Connecticut, reached out to Schara on Grace’s website to share her own experience.

Riley’s and Schara’s stories share many similarities. Riley told The Epoch Times that her daughter with Down’s syndrome, 37-year-old Megan, was admitted to a hospital for COVID-19 and put on numerous tranquilizers and Fentanyl, as well as remdesivir.

Megan was also labeled as DNR, which Riley said she had never approved, and didn’t know until she got Megan’s records.

Megan died on Dec. 9, 2021, Riley said.

After discovering that the hospital had put Megan on DNR, Riley said it made her grief worse.

“Because they had her on DNR the whole time, I just keep thinking, did the doctors do everything they could to save her?” she asked.

Epoch Times Photo
Megan Riley, 2021. (Courtesy of Robin Riley)

‘There Was No Reason to Sedate Her’

For Schara, none of this is a coincidence, he said.

For the combination of meds given to Grace, the doctor had to order, a pharmacist had to sign off, the hospital medication alarm had to be overridden, and in Grace’s case, a 14-year ICU nurse delivered the lethal combination, Schara said.

“We were not provided informed consent about the drugs administered to Grace, nor did we know they were being administered in the first place,” Schara said. “There was no reason to sedate her. There was no reason to give her Lorazepam–an anti-anxiety drug–while she was knocked out from Precedex. There was no reason to give her morphine. The Nuremberg Code was created to ensure people would have informed consent in regard to any medical procedure, and to be able to opt out of such things. St. Elizabeth’s ignored providing informed consent and they ignored all the warnings in the package inserts.”

Schara first thought the hospital protocols leading up to her death were about the hospital getting federal reimbursements; however, now he suspects a motive much worse: hospitals are taking federal funding to enact COVID protocols that were not only killing the unvaccinated but the disabled, he said.

He cited one 2020 study from the UK Office for National Statistics that show that disabled people had made up about three-fifths of COVID-related deaths in England and Wales.

“Disabled females between nine and 64 were even more at risk, in comparison with non-disabled females in the same age group, with a rate of death 10.8 times higher,” he said.

He cited a 2021 report from the University of Minnesota’s Center for Infectious Disease Research and Policy that stated that intellectual disability is second to old age as a risk factor for COVID-19 deaths.

“In unadjusted analysis, compared with 431,669 patients without intellectual disabilities, the 127,003 patients with intellectual disabilities were more suspectable to hospitalization, intensive care admission, and death,” he said.

He’s collected several additional studies and articles that support the theory that the disabled are at higher risk.

Combining that with his own experience, he thinks the disabled with COVID-19 are purposely being murdered.

He points to an article from NPR that tells the story of Melissa Hickson, who claimed a hospital where her quadriplegic husband was admitted for COVID-19 denied him life-saving treatment because of his disability.

The Milgram Experiment

All these reports and studies connect for Schara, implying ominous motives funded not only by money, but blind obedience, he said, alluding to a set of experiments in the 1960s that tested how far a person would go to follow orders.

“In the Milgram experiments, these psychologists tested the willingness of the participants in how far they would go to administer electric shock treatment to their peers under orders from an authority figure,” Schara said.

The experiments were held at Yale University by Stanley Milgram three months after the start of the trial of German Nazi war criminal Adolf Eichmann.

Milgram’s intent of the experiments was to study the psychology of genocide, he explained in his reports.

‘Death Protocols’

Todd Callender, an international lawyer with Disabled Rights Advocates and legal counsel to Truth for Health Foundation, previously told The Epoch Times that the “death protocols” being enacted in hospitals are passed down hierarchically from the World Health Organization to the Centers for Disease Control and the National Institute of Health, using the Public Readiness and Emergency Preparedness (PREP) Act and Health and Human Services authorization to release funding for the declared pandemic that sets the protocols in motion.

From there, hospitals that are federally funded through the Centers for Medicare and Medicaid Services (CMS) use coding tied to NIH and CDC-written protocols. If those hospitals take that funding, they must follow those protocols, starting with ICD-10 codes (International Classification of Diseases).

According to Callender, the CDC and NIH protocols are based on the WHO’s 2005 International Health Regulations which directs each of its 196 signatory countries to cede all sovereign powers to the WHO in the case of a declared health emergency.

“The WHO then directs the various state health bodies—in this case, the CDC and NIH—on treatment,” Callender said. “This is why every country is responding in the same way at the same time globally; it’s a back door to a one-world dictatorial government.”

When these protocols are passed down to the hospitals that take funding, under the emergency declaration, patients’ rights are waived under the CMS COVID waiver program in conjunction with the PREP and CARES Act, giving participating hospitals legal immunity.

Patients admitted for a broken arm can be given a COVID-19 test that “will almost always come back positive,” then are admitted and put on an IV with a tranquilizer that lowers oxygen levels, which then justifies putting the patient into COVID isolation where the antiviral drug remdesivir—which Callender called “lethal”—is added to the bag before being moved into the intensive care unit where the patient is then given morphine and fentanyl while being deprived of nutrition, he said.

“Everybody talks about their fear of FEMA (Federal Emergency Management Agency) death camps,” Callender said.  “Well, they’re already here; they’re called hospitals.”

Each of these procedures brings in high federal reimbursements of up to hundreds of thousands of dollars, Callender said.

Tom Renz, an attorney with America’s Frontline Doctors and Make Americans Free Again—organizations that oppose unconstitutional federal health mandates—hosts his own show on Brighteon TV where he interviewed Schara.

He told The Epoch Times that, because the PREP and CARES Acts have been passed, it’s made it impossible to sue hospitals because they convey immunity to these hospitals.

“Through those acts, we’ve given hospitals as much immunity as we’ve given vaccine makers as long as the state of emergency is continuing,” he said. “And we’ve got to ask ourselves, why is there still a national emergency?”

In addition to immunity, hospitals get federal funding through the CARES Act, which gives a 20 percent increase in reimbursement to hospitals for inpatient stays resulting from COVID-19, Renz said.

“The laws are structured in a way that incentivizes hospitals to kill people,” Renz said. “The hospital makes more money if you die from COVID-19 than if you recover from it. Why don’t we incentivize hospitals for getting people cured of COVID?”

Renz supports Schara’s conclusion that the hospital killed Grace, he said.

“Can you imagine watching your daughter die on Facetime, begging the hospital to revive her, and they say, ‘No, we are not going to do that,’ claiming that they have a DNR that you didn’t agree to?” he asked. “I mean, can you imagine the horror? No person should have to go through that, and we’ve got to have accountability.”

Like Schara’s response from the hospital, Riley said the hospital contended that the family agreed to the DNR.

In a Dec. 15 letter to the Schara family, the hospital said that “multiple and in-depth discussions and explanations occurred with you, your wife and family in regards to resuscitation and intubation. The medical record documentation on October 13, 2021, reflects additional discussion and confirmation of the family decisions related to resuscitation and intubation interventions should Grace’s condition deteriorate.”

“What a bunch of crap,” Schara said, reemphasizing that his family never agreed to a DNR.

“The doctors only discussed the concept of DNR,” Schara said. “Why would we agree to a DNR when he just got done telling us that Grace had such a good day yesterday that we should work on nutrition?”

St. Elizabeth’s Hospital did not respond to The Epoch Times’ request for comment.

‘Genocide’

There’s a pattern, Schara said, that he hasn’t been able to ignore.

“If I would have listened to me saying these words now seven months ago, I would have thought, at best he’s become a conspiracy theorist; at worst: a whack job,”  he said.

However, too many incidences of negligence have lined up to be a coincidence, he said.

“At first I thought this was about money, but it’s clear to me now that money was used to simply grease the wheels to accomplish a bigger agenda, which, in my opinion, is genocide,” he said.

Matt McGregor

REPORTER
Matt McGregor covers news from North and South Carolina for The Epoch Times. Send him your story ideas: matt.mcgregor@epochtimes.us

 

“Only the individual can rise to the heights of consciousness and awareness.

The more you belong to the crowd, the deeper you fall into darkness.”

Osho

 

 

 

Pfizer admits to fraud in court; Ex Pfizer Scientist Dr. Mike Yeadon; The midterms are the current task at hand; Protect Your Brain; Law of One

Pfizer admits to fraud in court


Ex Pfizer Scientist Dr. Mike Yeadon on what the covid vaccines were designed to do and how we the people need to standup and say no. It is time for Nuremburg 2.

Pilots come forward to call out the lack of safety from the Covid vaccines.


Kash was asked about Trump saying, “we caught them all,” and when that information will be released.  Kash answered with, “in Trump time.” He explained the importance of leadership changes within the agencies & departments that run the government.  The midterms are the current task at hand, so go vote!

HEALTH

Protect Your Brain With These Natural Substances

Several plant compounds have been shown to prevent or treat neurological decline
BY GREENMEDINFO TIMEJUNE 14, 2022

Your brain is command central for nearly all your body’s normal waking functions.

It’s the most complex organ in the human body, possessing around 100 billion neurons (nerve cells) and more than 100,000 miles of blood vessels. It’s responsible for controlling such functions as walking, talking, thinking, and breathing. Therefore, protecting the brain is a matter of life and breath.

A healthy brain is crucial at any age, but it is particularly important to safeguard when the brain is still forming (up to age 25) and in older adults. If you’re having lapses in memory and attribute it to “senior moments,” the signs of mild cognitive decline (MCD) may already be in effect.

But don’t worry—numerous studies have linked specific natural substances to delaying and even reversing MCD. Read on and learn how to protect your all-important brain with these six naturally neuroprotective substances.

Curcumin

The natural plant compound responsible for turmeric’s bright orange color, curcumin is a powerful antioxidant linked to dozens of beneficial health effects. One purported benefit that has been extensively researched is curcumin’s ability to protect the aging brain, an important effect at any age, especially when symptoms of dementia are present.

A 2012 study published in Ayu on the effects of turmeric on Alzheimer’s disease patients with severe behavioral and psychological symptoms of dementia showed that patients “improved remarkably” as a result of consuming 100 milligrams (mg) of curcumin daily for 12 weeks.

Symptoms such as agitation, anxiety, apathy, and urinary incontinence began improving after patients were prescribed turmeric powder capsules, without any adverse reactions noted. After three months of treatment, neuropsychiatric scores showed that symptoms were less acute and the burden on caregivers had lessened. After one year on the turmeric supplement, patients had not experienced a return of prior symptoms of dementia.

Ginsenosides

While you may not be familiar with their name, ginsenosides are potent plant compounds that have been isolated from a plant called Panax, which is widely known for its healthy roots—ginseng. Responsible for the pharmacological effects of ginseng, ginsenosides play a critical role in the body’s inflammatory and disease responses and are featured in a deepening catalog of research that may help prevent and treat inflammatory diseases, including those affecting the brain.

A recent study published in Frontiers in Pharmacology explored the effects of ginsenosides and their probable neuroprotective mechanisms in ischemic strokes, the most common type of stroke. These strokes occur when a blood vessel leading to the brain is obstructed.

After an exhaustive meta-analysis evaluating the effects of ginsenoside-Rb1, researchers concluded that ginsenosides have a potential neuroprotective effect that works through an array of mechanisms, including attenuating brain water content, promoting neurogenesis, reducing cell death, and providing antioxidative, anti-inflammatory effects. G-Rb1 also supplemented energy and enhanced cerebral circulation.

Ginkgo Biloba

Ginkgo biloba has a long history as a natural health aid, with anecdotes describing its use for asthma and bronchitis as far back as 2600 BCE. Most ginkgo biloba supplements are made from the leaves of the ginkgo tree, one of the longest-lived tree species on the planet, dating back more than 200 million years. A single ginkgo tree can live for as long as 1,000 years, so is it any wonder these trees may help improve your memory?

A 2015 meta-analysis published in the Journal of Pharmaceutical Health Care and Sciences looked at the efficacy and safety of ginkgo biloba extract for the treatment of dementia. It found that taking a 240-mg daily dose of ginkgo biloba extract is effective and safe in the treatment of patients with Alzheimer’s disease complicated by dementia, as well as vascular and mild forms of dementia.

A human trial on healthy, active young men found that six weeks’ supplementation with ginkgo biloba provided a boost in athletic performance, endurance, and antioxidant capacity. The study, published in Archives of Medical Science in 2015, found ginko also elicited better neuroprotection through increased exercise-induced production of brain-derived neurotrophic factor, a biomarker that serves to modulate brain activity and plays a part in neuroplasticity, the ability of the brain to regenerate in a healthy manner.

Resveratrol

Like curcumin, resveratrol is a natural plant polyphenol responsible for the deep color of wine, grapes, and red and blue berries. Known to pack an antioxidant punch, resveratrol has been synthesized into supplement form with promises to remedy everything from overweight to heart disease. But what does science say about this trendy panacea when it comes to brain health?

2017 Australian study tested whether chronic supplementation with resveratrol could improve brain function, cognition, and mood in post-menopausal women. Eighty women aged 45 to 85 years were randomized to receive resveratrol or placebo for 14 weeks. Effects on cognitive performance, cerebral blood flow, and arterial stiffness in the middle cerebral artery were measured.

Cerebrovascular responsiveness (CVR) to both cognitive testing and hypercapnia (excessive carbon dioxide in the blood) were also assessed, and mood questionnaires were administered. Compared to placebo, resveratrol elicited 17 percent increases in CVR to both hypercapnic and cognitive stimuli. Performance on cognitive tasks for verbal memory significantly improved, as did overall cognitive performance.

Mood also improved in multiple measures, indicating that regular consumption of a modest dose of resveratrol may enhance both cerebrovascular function and cognition. Researchers posited that resveratrol supplementation could potentially reduce the heightened risk of accelerated cognitive decline in post-menopausal women and offers a promising therapeutic treatment for this population group.

Melatonin

Melatonin has garnered fame as a natural sleep-aid, but did you know that it also protects the brain? A naturally occurring hormone that helps regulate the sleep-wake cycle, melatonin is a neuroprotective agent that may hold therapeutic promise for brain disorders such as Alzheimer’s, Parkinson’s, and stroke.

Secreted by the pineal gland in the brain, melatonin can also be taken as a supplement. Supplementation has been shown to reduce the incidence of delirium in older adults. A 2018 meta-analysis of both human and animal studies provided clinical evidence that melatonin treatment after traumatic brain injury (TBI) can significantly improve both pathological and behavioral outcomes in TBI patients. Observed results, published in BMC Geriatrics include reduced size of contusions and cerebral edema, and enhanced cognition.

The journal Neural Regeneration Research published a 2021 animal study on the effects of melatonin on rats with induced Alzheimer’s disease. Rats were administered 30 mg of melatonin per kilogram (kg) of body weight for 13 consecutive days.

Melatonin supplementation ameliorated learning and memory impairments on maze tests, improved the morphology and density of microvessels in the brain, alleviated pathological injuries of cerebral neurons, and decreased the expression of vascular endothelial growth factor and its receptors. Researchers concluded that melatonin supplementation can improve the cognitive function of patients with Alzheimer’s disease.

Cannabidiol

Cannabidiol, or CBD as it’s commonly known, is an isolated active compound in the cannabis plant that has been shown to effectively treat insomnia, pain, and brain disorders such as anxiety and epilepsy. Despite demonstrating such powerful effects on the brain, CBD is non-psychoactive, meaning it won’t get you high. But according to the latest medical science, it may possess strong neuroprotective properties to support your brain as you age.

Studies on CBD as an adjunct treatment for Parkinson’s disease patients have yielded promising results. Published in the Journal of Psychopharmacologya 2009 study tested six Parkinson’s patients and found that doses of CBD ranging from 150 mg to 400 mg over four weeks produced significant improvements in psychosis episodes and symptoms.

In 2014, researchers conducted a double-blind trial with a group of 21 Parkinson’s patients receiving either CBD at 75 mg/day, 300 mg/day, or placebo for six weeks. Increases in well-being and quality of life were observed in the 300 mg/day group versus the placebo group. Researchers hypothesized that these improvements may have been due to cannabidiol’s “anxiolytic,” “antidepressant,” “anti-psychotic,” and “sedative” properties.

CBD isn’t the only active plant compound in the cannabis plant (collectively called “cannabinoids”) that is proving its value to medical researchers. THC, the cannabinoid that conveys marijuana’s psychoactive properties, has been found to be superior to prescribed drugs in the treatment of Alzheimer’s disease. In their findings, published in Molecular Pharmaceutics, researchers attribute this compelling discovery to a “previously unrecognized molecular mechanism through which cannabinoid molecules may directly impact the progression of this debilitating disease.”

The GMI Research Group is dedicated to investigating the most important health and environmental issues of the day. Special emphasis will be placed on environmental health. Our focused and deep research will explore the many ways in which the present condition of the human body directly reflects the true state of the ambient environment. This work is reproduced and distributed with the permission of GreenMedInfo LLC. Sign up for the newsletter at www.GreenmedInfo.health

 

People Who Pushed Idea of Universal Vaccination Are ‘Guilty of Crimes Against Humanity’; 2000 Mules and More

People Who Pushed Idea of Universal Vaccination Are ‘Guilty of Crimes Against Humanity’: Former Pfizer VP

By Enrico Trigoso
May 14, 2022 Updated: May 14, 2022

 

Former Pfizer VP Michael Yeadon maintains that since the infection fatality ratio of COVID-19 has not been high, the vaccines should not have been mandated.

Moreover, he heavily blasted the corporate media mantras that designate these as safe, effective, and necessary to end the CCP (Chinese Communist Party) virus pandemic.

Yeadon is a big pharma veteran with 32 years in the industry. He worked as the head of allergy and respiratory research at Pfizer from 1995 to 2011 and is the former founder and CEO of Ziarco, a biotech company acquired by Novartis. Furthermore, he has a doctorate in respiratory pharmacology and holds a Double First Class Honors degree in biochemistry and toxicology.

A shocking 1,223 deaths and 42,086 adverse events were reported to Pfizer from the first day of the Pfizer-BioNTech vaccine rollout on Dec. 1, 2020, to Feb. 28, 2021.

“The worst flu season over the last decade is worse than [the threat] posed by this new virus,” Yeadon told The Epoch Times via email.

“And what do we do in response to seasonal influenza? Well, nothing really, beyond offering—and not mandating—vaccines which aren’t much use.”

Of important note is that the exact number of fatalities in China, where the virus originated, has been suppressed by the communist regime and could be 366 times the official figure.

Bill Gates, Dr Fauci And Big Pharma Accused Of Crimes Against Humanity In Complaint To International Court

Yeadon said that being sure the vaccines would cause no harm in the long run should have been imperative.

“It was never appropriate to attempt to ‘end the pandemic’ with a novel technology vaccine. In a public health mass intervention, safety is the top priority, more so even than effectiveness, because so many people will receive it,” Yeadon states in a document he sent to The Epoch Times.

“It’s simply not possible to obtain data demonstrating adequate longitudinal safety in the time period any pandemic can last. Those who pushed this line of argument and enabled the gene-based agents to be injected needlessly into billions of innocent people are guilty of crimes against humanity.”

Yeadon argues that natural immunity was obviously stronger than any protection from the jabs, and cited an article by Dr. Paul Alexander that has over 150 studies attesting to naturally acquired immunity to COVID-19.

Yeadon feels that the novel vaccines should have not been given emergency use authorization (EUA) and that if he were directing the pandemic response, children, pregnant women, and people who already had contracted the virus would have been given a red light on the jabs.

“I would have outright denied their use in children, in pregnancy, and in the infected/recovered. Point blank. I’d need years of safe use before contemplating an alteration of this stance.”

10 biggest crimes against humanity: Genocide, massacre, civil wars 

He further argues that the vaccines were sure to be toxic and it was only a matter of degree of toxicity.

“Having selected spike protein to be expressed, a protein which causes blood clotting to be initiated, a risk of thromboembolic adverse events was burned into the design. Nothing at all limits the amount of spike protein to be made in response to a given dose. Some individuals make a little and only briefly. The other end of a normal range results in synthesis of copious amounts of spike protein for a prolonged period. The locations in which this pathological event occurred, as well as where on the spectrum, in my view played a pivotal role in whether the victim experienced adverse events including death,” Yeadon said.

“There are many other pathologies flowing from the design of these agents, including for the mRNA ‘vaccines’ that lipid nanoparticle formulations leave the injection site and home to liver and ovaries, among other organs, but this evidence is enough to get started.”

Kiev Has Killed 14,000 Civilians Since 2014, Guilty of Crimes Against Humanity, Morales Says

Earlier this month, a physician said that he has been seeing an unusual amount of fetal death and miscarriages linked to the COVID-19 vaccines—according to his observations—and noted that mRNA products, contained in nanoparticles, accumulate in the ovaries.

“From data that we have, there appears to be a concentration of the lipid nanoparticles, which are very, very small particles, which are in the vaccine that are injected into the arm,” Dr. James Thorp told The Epoch Times, “and then the vast majority of those are dispersed throughout the entire body.”

A lipid nanoparticle is a fat-soluble membrane that is the cargo of the messenger RNA.

“They appear to concentrate in the ovaries, and they appear to cross all God-made barriers in the human body, the blood-brain barrier, the placental barrier during pregnancy, into the fetal bloodstream, and all the fetal tissues inside the womb, crossing the blood-brain barrier in the fetus, the baby in the womb, which is very concerning,” he noted, since the eggs produced by women are limited in number, and they would be “exposed to a potentially disastrous toxic lipid nanoparticle.”

Another concern that Yeadon had not noticed during his initial study was that “the mRNA products (Pfizer & Moderna) would accumulate in ovaries.”

“An FOI request to the Japanese Medicines Agency revealed that product accumulation in ovaries occurred in experiments in rodents,” Yeadon said. “I searched the literature based on these specific concerns and found a 2012 review, explicitly drawing attention to the evidence that the lipid nanoparticle formulations as a class do, in fact, accumulate in ovaries and may represent an unappreciated reproductive risk to humans. This was ‘a well known problem’ to experts in that field.”

A 2012 study says that after testing with different mouse species and Wistar rats, “a high local accumulation of nanoparticles, nanocapsules, and nanoemulsions in specific locations of the ovaries was found in all animals.”

Referring to the study, Yeadon told The Epoch Times that “the authors tell untruths. They say something like ‘there was no increase in anti-syncytin-1 antibodies.’”

“No, that’s wrong. Their data is clearly 2.5X increased after vaccination and obviously statistically significant (functional significance is looking confirmed by the miscarriage rate),” Yeadon noted.

“What they’ve done is cute. They’ve chosen a completely arbitrary level they scribed on the figure below which they claim nothing matters. No evidence whatsoever for that claim. In fact, in the discussion, they confess we don’t know the relationship between antibodies and the impact on function.”

Yeadon believes that the pharmaceutical industry “definitely knew,” since 2012, that the lipid nanoparticles would accumulate in the ovaries of women that took the vaccines.

“No one in the industry or in leading media could claim ‘they didn’t know about these risks to successful pregnancy.’”

Another recent study found that Pfizer’s COVID-19 vaccine goes into liver cells and is converted to DNA, a process called reverse-transcription.

Enrico Trigoso

REPORTER
Enrico Trigoso is an Epoch Times reporter focusing on the NYC area.
Attorney Thomas Renz

 

Hemp and Cannabis were put on this planet to meet all of our needs for food, medical,  textile, paper, construction. etc.

The elites  got rid of one of the most versatile crop to replace it with inferior ones  and gave us plastics.

This was done intentionally so they can profit, make the planet suffer and cause harm to us.

Support businesses selling hemp materials in order to help save our planet.

BREAKING: Evidence of Biden Payments from China Support Tony Bobulinski and Show the Bidens Made Millions Swindling America

Jordan Peterson “Something Big Is About To Happen”; Behind Disney; COVID Persists – What About the Vaccine?; 2000 Mules Trailer

“Something Big Is About To Happen” [PREPARE NOW!!!] Jordan Peterson (2022)


Behind Disney


COVID Persists – What About the Vaccine?

Analysis by Dr. Meryl Nass

This article was originally published here.

COVID persists, but the COVID vaccine narrative has taken on so much water, the powers that be have stopped bailing, and are going to let these vaccines slowly sink. But what do they have in store for us next?

There has been so much bad news about the vaccines in the last few months, it even leaked into the mainstream media. I think the cabal’s plan, at least in the US but probably everywhere, is to stop propping the ludicrous vaccine claims up and allow them to die a natural death. I explain why below.

Reality Check

There was just too much bad news, too few getting boosted, too much resistance from parents. Getting 8 or 10 doses into everyone was not going to happen. The terrified obedient masses were becoming fewer and fewer.

For example, here is one story that got lots of traction: ABC News covered the fact that “At least 72 COVID cases in the fully vaccinated resulted from the Gridiron dinner.” Not only did Nancy Pelosi test positive, but several members of Biden’s Cabinet and many other Beltway glitterati did too. All of whom had to have been vaccinated in order to attend.

There was plenty of happy talk that the afflicted politicians in DC had only mild COVID cases. Good for them. But, if vaccinations caused them to become asymptomatic spreaders instead of spreaders with symptoms, who would know to stay home while sick, the vaccines could actually be doing more harm than good in terms of transmission. They could be causing more COVID cases, not less.

By now, it has to be apparent to everyone who walks by a newsstand or turns on the TV that the media are begging much too hard for more shots.

It must be obvious to all that the shots do not prevent spread and therefore there is no logical way you can mandate them. Because if my shot does not protect you (and only with lots of fairy dust will it protect me) why would you have any interest in whether or not I am vaccinated?

Once you stop caring about my vaccination status, the cabal’s nexus of control starts to fall apart. That was their ace in the hole. Time for them to move on to something else.

A Crime Has Been Committed

The kicker for childhood vaccines: the New York state Department of Health study of vaccine efficacy in children. After 2 months, efficacy in the 5-11 year olds had fallen to 12%. In other words, 7 out of 8 vaccinated kids derived no benefit after 2 months, only risk.

The data were derived from 365,000 children, and apparently there was no way CDC could spin them, or 12% was the best spin they could put on the data. This report is a huge obstacle to universal child vaccinations. They cabal cannot surmount it.

It is important to mention again — because we keep forgetting — that while the vaccines are nominally licensed for adults, in fact you can only find the EUA (unlicensed) product in the US, and legally an EUA is experimental — and therefore forcing someone to be vaccinated is a Nuremberg violation and a violation of federal law.

The imposition of mandates for these experimental gene therapy products is therefore a crime, being committed by states, federal government and certain companies and other institutions. It seems that because US law was not designed for situations in which the government is the criminal, it has been very difficult to use the judicial system to change what is happening.

But surely if this persisted much longer an honest judge somewhere would finally rule that the vaccines are experimental and the COVID mandate house of cards would then collapse. Like Humpty Dumpty (it is Easter today after all):

“All the king’s horses and all the king’s men couldn’t put COVID mandates together again.”

Deaths Are Piling Up

What else has been happening that undermines the vaccine story? Well, in addition to all the collapsing athletes, there is now a large collection of mayors suddenly dropping dead throughout Germany.

In Australia, Queensland’s health minister just admitted that ambulances are being summoned for a lot more calls for cardiac events and sudden deaths: 40% more to be exact. Thanks to Igor Chudov for following this story, and including a video of the clueless minister admitting it, but having no idea why …

Then there were the 3 insurance companies, one each from the US, India and Germany, that admitted there were about 40% more deaths than expected in working-age people in the second half of 2021. The German official who blew the whistle, a CEO or VP, was immediately fired, which is a strong indication he was telling the truth.

Three doctor whistleblowers released a large cache of data from the military’s DMED database showing huge increases in service-member deaths. There has been a lot of confusion about these data. In part, that is because the military then reissued its data for the preceding several years, making the 2021 comparison look less dire. Mathew Crawford has some ideas about what really happened to the data.

The only thing that is absolutely clear so far is that there has been a coverup, and the health of vaccinated members of the military appears to have taken a dive. But we don’t know how deep.

Myocarditis — Conspiracy Theory No More

Everyone in the world must have heard the term ‘myocarditis’ by now, and knows that it is a vaccine injury. A lot of people also know that CDC Director Rochelle Walensky said post-vaccination myocarditis was extremely “rare but mild,” except it isn’t and she lied. The rate of myocarditis she cited is at least 10 times too low. About 1 in 2000 young men aged 18-24 sought care for this diagnosis after getting their second mRNA shot.

In fact, CDC was so intensely worried about blowback regarding its recommendation to vaccinate teens (despite the risk of myocarditis) it got the heads of about 20 professional medical organizations to sign on to a declaration supporting CDC’s recommendation. Wonder how much CDC paid for that. Getting such back-up was an unusual move, but perhaps unsurprising for risk-averse bureaucrats who worry about their own butt but not anyone else’s.

Rochelle even mentions these “cosigners” from many medical organizations in her ABC-TV interview. Collecting a bunch of “co-signers” is actually the proof that CDC knew its vaccine recommendation was going to considerably harm children.

While no one in a federal health agency has admitted it, many people must be aware that myocarditis is only the tip of the COVID vaccine injury iceberg. Myocarditis got attention because it’s life-threatening and almost always happens within 4 days of the second shot — it can’t be written off as coincidence, the way heart attacks, strokes, pulmonary emboli, sudden deaths and perhaps many other diagnoses have been.

As if there wasn’t enough bad vaccine news, there was information from the Medicare database that FDA posted last July, but it only recently got attention. FDA revealed that heart attacks, pulmonary emboli, disseminated intravascular coagulation (DIC, a life-threatening, bleeding plus clotting disorder) and ITP (another bleeding disorder) were related to the Pfizer vaccination in Medicare beneficiaries.

FDA promised to study this rigorously, but instead remained silent, and subsequently has never denied the relationship.

Ivermectin Success Stories Abound

And then there is ivermectin. So many ivermectin stories have been leaking into the popular press. Tennessee’s legislature made ivermectin essentially an over-the-counter drug last week. New Hampshire’s house voted in favor of this as well, while the NH Senate is now taking it up. Several states gave healthcare providers an immunity guarantee for the use of ivermectin and hydroxychloroquine for COVID.

Kansas’ Senate voted to strengthen religious exemptions and give safe harbor to those prescribing ivermectin, effectively undermining school vaccine mandates if it is enacted. Kansas also refused to enforce any adult vaccine mandates.

Coupled with stories about lawsuits against hospitals for refusing to supply ivermectin to dying relatives, like this one, people are finally realizing there is probably something to this drug, and they have been cheated. They were given a shot that barely works, is unsafe, and they were stopped from getting the good drug. And what if they lost their business to the lockdowns?

There must be a lot of anger simmering by now. I imagine the Great Reset cabal must be worried about this, and has decided to loosen its grip for the moment and hopefully let off some citizen steam.

The Tide Is Turning

There is more surprising vaccine news. While many institutions are still imposing mandates (and we need to find out what $ carrots were given to universities and other entities to impose illegal mandates of experimental vaccines) in other, surprising places the mandates are disappearing. Out west in Woke Land, the Washington state Department of Health said it would not require COVID vaccines to attend school after all.

Despite Gavin Newsom’s 2021 executive order mandating vaccines for school kids as soon as they are licensed, California’s Department of Health has just done the same thing that Washington’s did: killed the COVID vaccine mandate for the 2022-23 school year.

Finally, Fauci himself and various media now openly admit the vaccines will not take us to herd immunity (no matter how many shots we get).

This is why I am convinced the ship is turning and the current vaccine programs will be scuttled. Those states’ health departments take their orders from CDC and DC. I do not think FDA is going to be issuing any more fake licenses for COVID vaccines.

[I say fake because a) the vaccines do not meet licensure criteria, and b) after issuing the Moderna and Pfizer vaccines licenses for adults, neither licensed product has been distributed in the US for actual use]. The Advisory Committee meeting to deliberate on vaccines for kids aged 6 months up to 5 years was delayed from February to April, and now from April till June. It seems like our unvaxxed kids will be spared. Hallelujah!

Invalid Surrogates Used for the EUAs

During the April 6, 2022 Vaccine and Related Biological Products Advisory Committee (VRBPAC) meeting, which I live-blogged and summarized, both briefers and committee members acknowledged that the neutralizing antibody titers that have been used as a surrogate for immunity in order to issue EUAs, were in fact not valid surrogates.

This had been obvious for awhile, but a recent Israeli study in healthcare workers made it crystal clear. While neutralizing antibody titers rose tenfold after a fourth vaccination, by 2 months out the Pfizer vaccine had only 30% efficacy against infection, and the Moderna vaccine had only 11%. So the high antibody titers were, in fact, meaningless.

This is really important, because Pfizer and Moderna have been relying on titers to get their vaccines okayed for the younger age groups, those below 16 and 18 respectively. They don’t have data showing the vaccines are actually reducing cases by 50% or more, which is the standard FDA said was necessary. They don’t have data showing that the vaccines prevent serious cases or deaths, another standard.

Up until now, FDA accepted titers in lieu of actual efficacy results from clinical trials to issue its EUAs for children — but with the recent VRBPAC admissions, which must have been planned in advance (otherwise why did multiple people at the meeting discuss it as settled fact when they had never mentioned it before?) FDA can no longer do so.

Another thing that happened at the VRBPAC meeting was that Peter Marks, the head of FDA’s Center for Biologics and highest FDA official there, said that if a new type of COVID vaccine is developed for the next booster, then the current vaccines would no longer be used, because it would be too confusing (according to STAT). Too confusing?! I believe this was another effort to prepare us for the demise of the current mRNA vaccines.

The fall of the vaccines means the fall of the vaccine passports. This ought to slow down the imposition of CBDCs and all-digital money for a bit. If we don’t have to show our vaccine certificate to go shop, eat, etc., (and people stop being fearful of catching something from each Other) people will be a lot less inclined to “show their papers” to go about their lives. It’s our job to explain over and over that this was how the Nazis maintained control.

Here I Read the Tea Leaves

If there is a new vaccine waiting in the wings, FDA and its briefers were not telling us about it at the VRBPAC meeting, which was the time to do so. For right now, I think the current crop of vaccines and the vaccine passports are going away. I don’t think the authorities anticipate another severe COVID wave in the foreseeable future … as most people now have Omicron immunity. The COVID fear will dissipate.

The original Wuhan strain appeared out of nowhere. No natural progenitor could be found. And the original Omicron strain appears to have also originated in a lab. If I was a member of the Great Reset cabal, I would be quite hesitant about releasing yet a third lab-engineered virus on the population. Because millions of people will be looking for one, and it won’t take long before its laboratory provenance is discovered. Then the pitchforks might really come out.

On the other hand, I do believe the cabal has bet the farm on their Reset, they can’t go back, and they are simply moving on to another means of accomplishing it besides COVID. The over-the-top WHO Treaty/Constitution and its amendments designed to assume sovereignty over the world in the event of a pandemic is an ambitious Plan B.

But I don’t think it will fly. Too many people know the WHO was wrong about virtually everything regarding management of this pandemic, not to mention the 2009 swine flu. And then there was that little matter of WHO undertaking the SOLIDARITY Trial, in which WHO officials deliberately poisoned over 1,000 COVID patients with excessive doses of hydroxychloroquine and in many cases failed to obtain signed informed consents. The WHO could be liable for manslaughter.

Will Russia and China really agree to give up their sovereignty to Tedros? China, maybe. Brazil? India? Indonesia? Japan? Nigeria? Can all of their leaders, and their local power centers, have been sufficiently corrupted to turn over their nations to the cabal? I think that could be a stretch.

I suspect the cabal will try their best to get a legal OK to take over the world with the upcoming WHO pandemic treaty, but it won’t fly. Too many people already know about these plans.

What’s Plan C?

After the WHO, the cabal will move on to something else, Plan C. Climate catastrophe? Yet more wars? Aliens? I’m guessing it will be a few years before we get hit with another nasty bug. By then maybe the fiat currencies will have finally crashed, and the cabal won’t have as tight control of the reins. By then, Fauci, Walensky, Biden, Macron, Johnson, Trudeau, Draghi will hopefully be unpleasant memories.

I am not thinking we will all sing kumbaya. I expect a good deal of misery as the cabal pushes all the levers at its disposal.

The Shanghai city and port closure (China’s largest city and the world’s largest port) seems to me a deliberate attempt to interfere with worldwide transit of goods and to reduce food availability. The Chinese know how to treat COVID. They make the drugs and herbs. There is no need for them to lock down.

Don’t miss all the food warehouses that caught fire recently, or the refusal of the Union Pacific railroad to carry 20% of the fertilizer the US’s biggest fertilizer producer expected to ship.

We are finally understanding that the awful government policies were deliberate — intended to cement control over and impoverish us. But maybe we can start to build something a whole lot better.

We are shaking loose of the educational indoctrination system, the ruination of our foods, the user-unfriendly and health-damaging healthcare system. We are starting to grasp that our governments acted with malice aforethought to stupefy and eventually enslave us.

People are breaking free and taking responsibility for their future. Where I live, people are learning self-sufficiency skills, creating home-schooling coops, building greenhouses and growing food. The migration to the countryside was deliberate.

A better life? It just takes everybody waking up. Despite all the acrimony we have faced, the time is ripe to help our fellows see things clearly. We have to love them, help them, meet them where they are. Maybe it is just to talk about the Gridiron dinner. Or ivermectin. They won’t get it in a day. But keep trying. It is our only solution.

2000 Mules Trailer

https://2000mules.com/

Get Vaxxed or Pay; Pfizer Cherry Picked Data; Biden’s Dirty Dealings; “2000 Mules” Proves Large-scale, Illegal Vote Trafficking Occurred in the 2020 Election; US Government Frets Over Musk-owned Twitter

Rhode Island Bill S.2552 Would Require Residents to Be Vaccinated or Pay Fines & Double Personal Income Taxes

Violating the proposed vaccine mandate would come with a price. Violators would face “a civil penalty of $50 and shall owe twice the amount of personal income taxes.”

Employers would be responsible for enforcement, requiring workers to provide proof or face a $5,000 fine for each unvaccinated worker.


Pfizer’s Cases Gone Missing and Cherry-Picked Subjects: Data Shows 71% of People Tested Were Women. Dr. Naomi Wolf: “52% of the human beings in the world are female, so they’re cherry picking who the subjects are. Why would they leave out men? Well, one obvious answer is men get myocarditis [disproportionately].”

Based on another study the fully jabbed are up to 2x more likely to be hospitalized with Covid-19 and 2x more likely to die of Covid-19. Article (https://dailyexpose.uk/2022/04/24/gov-report-fully-vaccinated-suffering-ade-since-new-year/)


President of Hunter Biden’s Shell Corporation, Rosemont Seneca, Visited White House 19 Times After Creating $1B Fund w/ The Bank of China

https://rumble.com/v12c03h-president-of-hunter-bidens-shell-corporation-rosemont-seneca-visited-white-.html

Hunter Biden’s closest business partner made at least 19 visits to the White House and other official locations between 2009 and 2015, including a sit-down with then-Vice President Joe Biden in the West Wing.

Visitor logs from the White House of former President Barack Obama reviewed by The Post cast further doubt over Joe Biden’s claims that he knew nothing of his son’s dealings.


WHO finds potential link between COVID-19 vaccine and hearing issues


Filmmaker: Documentary Proves Rampant Illegal Vote Trafficking in 2020

By Steven Kovac
April 26, 2022 Updated: April 26, 2022

Filmmaker Dinesh D’Souza believes that evidence presented in his new documentary, “2000 Mules,” proves that large-scale, illegal vote trafficking occurred in the 2020 election.

D’Souza told The Epoch Times: “2000 Mules will settle the issue beyond a shadow of a doubt by using two powerful, independent modes of investigation. The evidence is so conclusive, so decisive, that it leaves nothing to argue about.”

The film opens in 300 theaters on May 2 and May 4.

D’Souza, who is a contributor to The Epoch Times, said an investigative team used cellphone tracking and video footage to prove that unauthorized intermediaries called “mules” collected thousands of absentee ballots from voters and deposited them in drop boxes for money, which is illegal in all 50 states.

Cellphones emit a unique and identifiable signal or “ping.” Trillions of pings were analyzed by investigators to reconstruct the movements of thousands of mules as they went about their work in the weeks prior to the 2020 presidential election, the documentary claims.

“Who would have ever thought that investigators could look back in time and discover such things?” D’Souza said.

Epoch Times Photo
Dinesh D’Souza attends the premiere of Lionsgate Films’ “America” at Regal Cinemas L.A. Live in Los Angeles on June 30, 2014. (Alberto E. Rodriguez/Getty Images)

Investigators also sifted through millions of minutes of video surveillance footage and were able to capture on tape numerous mules stuffing absentee ballot drop boxes, D’Souza said. The videos show the mules taking selfies of themselves as proof of services rendered to their employers in order to be paid, he said.

“Not all the drop boxes were under video surveillance, but enough were to provide incontrovertible evidence, much obtained from government entities,” he said. “’2000 Mules’ contains a lot of never-before-seen footage depicting glove-wearing mules moving from county to county delivering absentee ballots to drop boxes, often in the dead of night.”

Much of the film focuses on the state of Georgia, where, according to True the Vote—the organization that conducted the investigations—242 metro Atlanta mules made 5,668 stops at drop boxes during elections in late 2020.

drop box ballot
Residents drop mail-in ballots in a ballot box outside of the Tippecanoe branch library in Milwaukee, on Oct. 20, 2020. (Scott Olson/Getty Images)

Similar illegal activities were found in Arizona, Wisconsin, Pennsylvania, Texas, and Michigan, according to the group. True the Vote estimates that at least 4.8 million votes were trafficked nationally. The studies were funded by the human rights organization First Freedoms.

Election fraud has been committed by both parties throughout U.S. history, and therefore “cannot be considered abnormal,” D’Souza said. “The Democrats have a particular history of committing specialized election fraud in urban areas.

“The COVID-19 pandemic created an opportunity to do fraud on a scale not imagined before. The avalanche of absentee ballots sent out and the drop boxes presented much greater opportunity.”

D’Souza said he’s worried about the Democrats’ push to centralize how elections are conducted at both the state and national levels.

“A united Republican opposition is the only thing thwarting Biden, Pelosi, and the Democrats from enacting their plans,” he said. “Across America, the Democrats are trying to get rid of election security measures imposed by the states. They want to legalize fraud.”

The infusion of private money to help pay for elections is something D’Souza finds “very disturbing.”

“The money is largely coming from nonprofits funded by billionaires like Zuckerberg. They pose as politically neutral, which they are not.

“Localities were pressured by the nonprofits to have things like drop boxes as a condition for receiving millions of dollars in grant funding.”

D’Souza said that in November 2020, nonprofits paid for programs and advertising that actively encouraged “certain people to come out and vote.”

mark Zuckerberg in congress
Facebook co-founder and CEO Mark Zuckerberg testifies before the House Financial Services Committee in Washington, D.C., on Oct. 23, 2019. (Chip Somodevilla/Getty Images)

According to the Zuckerberg-funded Center for Tech and Civic Life, the money was given to help municipalities cope with public health challenges presented by the pandemic.

“Through the movie ‘2000 Mules,’ we are taking on the ultimate taboo in American politics today—saying that the 2020 election was stolen by systematic, organized fraud committed by the Democrats and the left,” D’Souza told The Epoch Times.

Mindful of the power of cancel culture, D’Souza said great care has been taken to release the film on what he calls “un-cancellable platforms.”

“It’s hard to believe we have reached that point in America, but alas, we have,” he said.

“While I was a writer or a figure in a think-tank, I wasn’t bothered much. It was when I began to reach a wider audience that I became a political target.”

When asked why he’s willing to subject himself to possible cancellation, D’Souza said, “I am defending the system which made it possible for an immigrant from India, a boy at the bottom, to make my way up—a system that makes this kind of upward economic and social mobility possible.”

D’Souza has produced numerous documentaries, three of which are ranked in the top 10 highest-grossing political documentaries of all time.

Steven Kovac

REPORTER

Steven Kovac is an Epoch Times reporter who covers the state of Michigan. He is a former small businessman, local elected official, and conservative political activist. He is an ordained minister of the Gospel. Steven and his wife of 32 years have two grown daughters. He can be reached at steven.kovac@epochtimes.us


US government frets over Musk-owned Twitter

The US government finds cause for alarm in “large social media platforms”
US government frets over Musk-owned Twitter

Billionaire Elon Musk’s acquisition of social media giant Twitter has seen the US government suddenly backing away from its embrace of such mega platforms. “No matter who owns or runs Twitter, the president [Joe Biden] has long been concerned about the power of large social media platforms [and] the power they have over our daily lives,” White House press secretary Jen Psaki stated during a press briefing on Monday after Musk officially bought Twitter for $44 billion.

Elon Musk buys Twitter

Psaki insisted this sudden concern was unrelated to the Tesla tycoon’s latest purchase, claiming “our concerns are not new” with regard to the social media monopolies. Biden, she said, “has long argued that tech platforms must be held accountable for the harm they cause.

The White House spokesperson insisted the administration was continuing to push for the repeal of Section 230 of the Communications Decency Act, which offers platforms that host third-party content immunity from liability for user-supplied content, as well as antitrust and transparency enforcement against the social media behemoths.

We engage regularly with all social media platforms about steps that can be taken,” Psaki claimed, adding that while she was “sure [this] will continue,” there were “also reforms that we think Congress could take.

While there are multiple antitrust cases pending against Facebook, Amazon, Google, and Apple, Twitter has been in the regulatory crosshairs somewhat less often. However, it has received plenty of attention as the former online home of ex-President Donald Trump, from which he was exiled in January 2021 following the January 6 riot at the Capitol while he was still commander-in-chief. Some fear a Musk-led Twitter will give him back his account, though he remains banned from other mainstream social media outlets.

However, Trump told Fox News on Monday he plans to focus on TRUTH Social, his own social media network that debuted earlier this year, and would not return to Twitter even if Musk reinstated his page. Trump has also been a vocal supporter of repealing Section 230, which would align him with the White House if Psaki’s statements reflect the administration’s genuine position.

However, the Biden’s team have in the past praised such monopolistic platforms, admitting government officials had personally flagged ‘misinformation’ related to Covid-19 on Facebook, even while calling on the tech giants to do more to silence unauthorized viewpoints.

Musk has promised to make free speech central in his takeover of Twitter, and took the unusual step of calling for his “worst critics” to stay on the service, insisting this is “what free speech means.”

While his purchase had some on the platform frothing mad, Twitter stock was up 6% on the announcement of the acquisition.

CIA Involvement in Ukraine; Hunter Biden’s laptop; Satanism in Hollywood; Biggest Scandal Since Watergate

Journalist and author Douglas Valentine on the history of the CIA’s involvement in Ukraine and it is not what we have been told.

Jack Maxley the whistleblower who had access to Hunter Biden’s laptop,  explains what some of the content on the Laptop.

Hollywood is the trap for many in the world of Satanism

 

 


 

The Scandal bigger than Watergate

Corona Investigative Committee

Pfizer Hired 600 Employees Due to ‘Large Increase of Adverse Event Reports’: Document

By Zachary Stieber
April 8, 2022 Updated: April 8, 2022

Pfizer hired 600 employees in the months after its COVID-19 vaccine was authorized in the United States due to the “large increase” of reports of side effects linked to the vaccine, according to a document prepared by the company.

Pfizer has “taken a multiple actions to help alleviate the large increase of adverse event reports,” according to the document. “This includes significant technology enhancements, and process and workflow solutions, as well as increasing the number of data entry and case processing colleagues.”

At the time when the document—from the first quarter of 2021—was sent to the U.S. Food and Drug Administration (FDA), Pfizer had onboarded about 600 extra full-time workers to deal with the jump.

“More are joining each month with an expected total of more than 1,800 additional resources by the end of June 2021,” Pfizer said.

The document was titled a “cumulative analysis of post-authorization adverse event reports” of Pfizer’s vaccine received through Feb. 28, 2021. It was approved by the FDA on April 30, 2021.

The document was not made public until the Public Health and Medical Professionals for Transparency sued the FDA after the agency claimed it needed decades to produce all the documents relating to the emergency use authorization granted to the company for the vaccine.

Under an agreement reached in February, the FDA must produce a certain number of pages each month.

The analysis of adverse event reports was previously disclosed to the health transparency group, but certain portions were redacted (pdf), including the number of workers Pfizer onboarded to deal with the jump in adverse event reports.

“We asked that the redactions on page 6 of this report be lifted and the FDA agreed without providing an explanation,” Aaron Siri, a lawyer representing the plaintiffs, told The Epoch Times in an email.

After the document was produced, the FDA determined that the three redactions on that page “could be lifted,” an FDA spokesperson told The Epoch Times via email.

The redactions had been made under (b) (4) of the Freedom of Information Act, which lets agencies “withhold trade secrets and commercial or financial information obtained from a person which is privileged or confidential.”

The unredacted version of the document also now shows that approximately 126 million doses of Pfizer were shipped around the world since the company received the first clearance, from U.S. regulators, on Dec. 1, 2020. The shipments took place through Feb. 28, 2021.

It was unclear how many of those doses had been administered as of that date.

Pfizer did not respond to emailed questions, including how many workers it has onboarded to deal with adverse events.

The companies that manufacture the other two COVID-19 vaccines that U.S. regulators have cleared, Moderna and Johnson & Johnson, did not respond when asked if they have seen an increase in adverse events and if they have hired more employees to deal with reports.

The number of post-vaccination adverse event reports to the Vaccine Adverse Event Reporting System, jointly run by the FDA and the Centers for Disease Control and Prevention, has spiked since the vaccines were first cleared.

Problems linked to the vaccines include heart inflammation, blood clotting, and severe allergic shock.

Federal officials say the vaccines’ benefits outweigh the risks, but some experts are increasingly questioning that assertion, particularly for certain populations.

Pfizer Saw So Many Adverse Events, They Had To Hire New Employees; Vaxxine Genocide Will Not Be Keep From The Masses Much Longer

Bombshell: Pfizer Saw So Many Adverse Events, They Had to Hire 2,400 NEW Employees to Process Them

Dr. Naomi Wolf: “[Pfizer] hid, they concealed, they redacted from disclosure, forced by court, the fact that they were processing so many adverse events in the first three months… that they had to hire 2,400 new employees. They hid that; they concealed it… the volume of bad outcomes, dangerous outcomes… there were so many [that] they couldn’t keep up with it with their own staff.”


ANOTHER COLLAPSE ON LIVE TV: THE VACCINE GENOCIDE WILL NOT BE KEPT FROM THE MASSES FOR MUCH LONGER

State-by-state breakdown of federal aid per COVID-19 case

HHS recently began distributing the first $30 billion of emergency funding designated for hospitals in the Coronavirus Aid, Relief, and Economic Security Act. Some of the states hit hardest by the COVID-19 pandemic will receive less funding than states touched relatively lightly, according to an analysis by Kaiser Health News.

The The first round of grants will be distributed based on historical share Medicare revenue, not based on COVID-19 burden. Therefore, hard-hit states like New York will receive far less per COVID-19 case than most other states.

HHS said it doled out the first slice of funding based on Medicare revenue to get support to hospitals as quickly as possible. The agency said the next round of grants “will focus on providers in areas particularly impacted by the COVID-19 outbreak,” rural hospitals and other healthcare providers that receive much of their revenues from Medicaid.

Below is a breakdown of how much funding per COVID-19 case each state will receive from the first $30 billion in aid. Kaiser Health News used a state breakdown provided to the House Ways and Means Committee by HHS along with COVID-19 cases tabulated by The New York Times for its analysis. link


 

Jacob Creech (aka @Bioclandestine) on the Connection Between Democrat Families & Biolabs in Ukraine

Clip: https://rumble.com/vzvf38-jacob-creech-on-the-connection-between-democrat-families-and-biolabs-in-ukr.html

Full Interview: https://battleplan.news/watch?id=624cb47ebc0dcd52c2f614c3


 

How the Tavistock Institute manipulates popular perception in order to shape society


Chemicals feminizing males, study suggests

Children Are Being Raped; Documents Pfizer Didn’t Want You To See; ‘100 Percent’ Vaccinated Cruise Ship Hit With COVID-19 Outbreak

“The borders being open are a nightmare. These children are being raped – this is what’s happening!”

Jason Sisneros on the Huge Spike in Child Trafficking Since Biden Took Office.  https://rumble.com/vyvb05-jason-sisneros-on-the-huge-spike-in-child-trafficking-since-biden-took-offi.html


“Nobody is going to trust these people ever again”

The Ingraham Angle: The Documents Pfizer Didn’t Want You To See


Thank God For Covid

‘100 Percent’ Vaccinated Cruise Ship Hit With COVID-19 Outbreak

By Jack Phillips
March 29, 2022 Updated: March 29, 2022

Princess Cruises confirmed that one of its cruise liners, the Ruby Princess, reported a COVID-19 outbreak before docking in San Francisco.

The cruise operator requires passengers and crew members to be fully vaccinated for COVID-19, which is caused by the CCP (Chinese Communist Party) virus. Princess Cruises also mandates passengers to show a negative COVID-19 test and proof of vaccination to board, according to its website.

Those who tested positive were “isolated and quarantined while monitored and cared for by our shipboard medical team,” Princess Cruises said in a statement to news outlets Monday. It did not say how many people tested positive or when they tested positive during the cruise.

“They were all asymptomatic or only mildly symptomatic,” the firm said. Some of the passengers who contracted the CCP virus did not finish their quarantine and were either sent home or “were provided with accommodations ashore to hotels coordinated in advance for isolation and quarantine,” the statement added.

“As with all Princess itineraries, this cruise is operated as a vaccinated cruise, as defined by the U.S. Centers for Disease Control and Prevention,” the company told the San Francisco Chronicle. “Guests and crew vaccination rates were at 100 percent.”

The Ruby Princess docked in San Francisco on Sunday, the company said, after the ship was on a 15-day cruise to the Panama Canal. The ship departed later that day on a 15-day cruise to Hawaii, said Negin Kamali, spokesperson for Princess Cruises, in a statement to USA Today.

Under the Center for Disease Control and Prevention’s (CDC) cruise ship monitoring website, the Ruby Princess is described as “under observation” by the federal health agency.

The development comes about two weeks after the CDC lowered its COVID-19 warning for cruise travel to “Level 2,” a “moderate” risk. Previously, the agency gave cruise travel a “Level 4” warning, which is the highest level, as the Omicron variant spread across the United States several months ago.

During the COVID-19 pandemic, the cruise industry has been battered by lockdowns and federal restrictions on cruises—amid early speculation that cruise ships were “super spreaders” of the virus. Industry data suggests that cruise companies collectively lost $63 billion in 2020 and 2021.

On March 18, the CDC released new COVID-19 guidelines for the cruise industry, with a spokesman telling USA Today that it entails the agency’s suggestions on social distancing, quarantine requirements, and port agreements.

The Epoch Times has contacted Princess Cruises for comment.

Jack Phillips

BREAKING NEWS REPORTER
Jack Phillips is a breaking news reporter at The Epoch Times based in New York.
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