1.) Major victory: Court rules airline cannot ask new pilots’ vaccination status
The Amsterdam Court of Appeal has determined KLM airline is no longer allowed to ask new pilots about their Covid “vaccine” status. According to the judge, among other things, there was no operational necessity for such a decision. Nevertheless, the association of Dutch Airline Pilots (VNV) is pleased with the Court’s decision and is celebrating its victory.
On Thursday, a judge declared that KLM would be fined 100,000 EUR per violation effective immediately. Thursday. In addition, the Court has immediately prohibited KLM from collecting and/or using Covid “vaccination” information in any way. In addition, the company is not allowed to reject candidates because they have not received the experimental mRNA injections.
The judge ruled that the infringement of the fundamental rights of candidates committed by KLM’s conduct in the application procedure is disproportionate because KLM has not been able to demonstrate that there is an operational necessity.
2.) Stacy Washington will be speaking at the Faulkner County Republican Women’s 6th Annual Flag Day dinner. On June 23rd @ 6:00 pm. If you would like tickets or more information please contact me 5015813560 or email rbmakeadifference@gmail.com
3.) FDA Sued Over Hiding Records From Moderna COVID-19 Vaccine Approval
Defending the Republic, a Texas-based non-profit filed a Freedom of Information Act lawsuit against the Food and Drug Administration for refusing to turn over records related to the approval of Moderna’s COVID-19 vaccines.
The group filed a Freedom of Information Act (FOIA) request seeking the production of records relating to the Food and Drug Administration’s (FDA) internal review process of Moderna’s COVID-19 vaccine marketed as “Spikevax.” Given that the forces impacting the FDA’s decision to authorize the vaccine could have influenced Americans’ decision on whether or not to get vaccinated against COVID-19, Defending the Republic requested expedited processing of relevant records.
“Please provide all data and information submitted by Moderna relating to the FDA review and approval of Spikevax. This includes, but is not limited to, all safety and effectiveness data and information; all data and information in the biological product file; and all ingredients,” outlined the initial FOIA request.
On February 9th, less than a week after the initial FOIA was filed, the FDA refused the request for expedited processing, prompting Defending the Republic to appeal the decision.
“The FDA declined the appeal, leaving Defending the Republic with no choice but to file this action seeking a court order requiring the FDA produce the requested records on an expedited schedule— just as those who obtained a court order for the expedited production of records relating to the FDA approved Pfizer-BioNTech vaccine,” explains a complaint filed by Defending the Republic.
Defending the Republic was especially interested in better understanding the review process for Moderna’s COVID-19 vaccine, as data has shown its risk were not adequately explained to those receiving it and data surrounding its efficacy remains obscured. As Defending the Republic explains:
Despite the FDA’s promises, a closer inspection of the Spikevax approval reveal there may be glaring issues in the approval process. The Spikevax package insert concedes “[a]vailable data on SPIKEVAX administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy.”
And while the FDA publicly pronounced that the “data demonstrated that Spikevax was 93% effective in preventing COVID-19,” the Spikevax fact sheet for recipients and caregivers provides important context omitted by the public officials: “The [Spikevax] duration of protection against COVID19 is currently unknown.
The lawsuit comes amidst several National Pulse exposés revealing how lobbyists from pharmaceutical companies including Moderna have entrenched themselves within Washington, D.C.
4.) Cancer Trial Using Monoclonal Antibody Finds Remission in Every Patient
A cancer trial has reportedly become the first in the world to completely remove the disease in every patient, according to a study published on June 5 in The New England Journal of Medicine.
The study, “PD-1 Blockade in Mismatch Repair—Deficient, Locally Advanced Rectal Cancer,” was conducted among 12 rectal cancer patients, all of whom had a “clinical complete response,” according to the authors, led by Dr. Andrea Cercek of the Memorial Sloan Kettering Cancer Center in New York.
Doctors have been unable to see any evidence of tumors among the patients when using magnetic resonance imaging, fludeoxyglucose F 18 injections, physical examinations, or endoscopic evaluations, according to researchers.
The patients also continued to show no signs of cancer during follow-ups ranging from six months to 25 months and haven’t had to undergo surgery or receive radiation and chemotherapy. “No adverse events of grade 3 or higher have been reported,” the study authors noted.
Specifically, the rectal cancer patients were given dostarlimab, a monoclonal antibody, every three weeks for six months. The patients had mismatch repair-deficient stage two or three rectal adenocarcinomas, a type of cancer.
Typically, such cancer patients would have needed to undergo often debilitating treatments such as chemotherapy, radiation, or surgery, and in extreme cases be fitted with colostomy bags. However, after taking dostarlimab, which is sold under the brand name Jemperli, no cases of progression or recurrence were reported in the patients who underwent the study.
Dr. Luis A. Diaz Jr. of Memorial Sloan Kettering Cancer Center, author of the study, told The New York Times that he believes this is the “first time this has happened in the history of cancer.”
As you know, the HD-25 election was stolen from Jody Harris in Crawford County. She is fighting back! Read her lawsuit below – you’ll get all the details and see just how corrupt the RINOs in Crawford County are.
A large study from Israel revealed that the Pfizer COVID-19 mRNA jab is associated with a threefold increased risk of myocarditis, leading to the condition at a rate of one to five events per 100,000 persons.
Other elevated risks were also identified following the COVID jab, including lymphadenopathy (swollen lymph nodes), appendicitis and herpes zoster infection.
When myocarditis occurs, it reduces your heart’s ability to pump and can cause rapid or abnormal heart rhythms that can be deadly. In severe cases, myocarditis can cause permanent damage to the heart muscle and lead to heart failure, heart attack, stroke and sudden cardiac death.
Due to the risk of myocarditis, Britain’s Joint Committee on Vaccination and Immunization (JCVI) recommended against COVID-9 injections for healthy 12- to 15-year-olds.
2.) Keeping Schools Open During Pandemic Helped Swedish Children Avoid Learning Loss: Study
There’s no evidence that Sweden’s youngest schoolchildren, who have never had to miss a single day in school because of the COVID pandemic, suffered any drop in their reading skills, a new study suggests.
When the CCP (Chinese Communist Party) virus first hit Sweden, the country’s public health authorities made it clear that daycare centers and primary schools, which serve students in grades 1 through 3, must stay open. Swedish government held on to that policy even after its COVID-19 death rates surpassed those of its Nordic neighbors.
Throughout much of the pandemic, Sweden’s response relied heavily on voluntary cooperation. Instead of imposing face covering and social distancing mandates on schools, it only recommended teachers and students to stay at home if they felt any symptoms of illness.
In a study published in the International Journal of Educational Research, a team of researchers at Stockholm’s Karolinska University analyzed data from 97,073 primary school students across Sweden. The goal was to investigate whether Swedish children suffered any potential learning loss during the 2020-2021 school year.”We conclude that there is no evidence of a learning loss regarding early reading skills in Swedish primary school students,” the researchers wrote. “In the light of international studies on reading skills in younger students during the pandemic, we conclude that the decision to keep schools open benefited Swedish primary school students,” they added.
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2.) DTR ask court to forcethe Department of Defense to produce documents
Defending the Republic have asked a federal court to compel the military – including the Department of Defense – to uphold their discovery obligations and produce documents requested on behalf of DTR’s military clients.
The case is Coker v. Austin, where a number of brave military service members have challenged the FDA’s “approval” of the Comirnaty COVID-19 “vaccine” and the DOD’s implementation of that policy.
Back in January, the court rejected their effort to prevent discovery into the execution of the military’s COVID-19 vaccine mandate. Faced with the possibility of damaging information being released, the Biden DOD now refuses to produce documents – in contravention of the court’s previous order.
DTR had no choice but to ask the court to compel the Biden DOD to produce the requested documents and records. As DTR made clear to the court, the Biden DOD cannot evade their legal responsibilities – especially when it comes to the safety of our military service members.
John Pierce Law has filed a lawsuit against Atlas Air, on behalf of US Freedom Flyers (USFF) and Atlas employees, and plans to sue all major airlines, 18 altogether, plus the Federal Aviation Administration (FAA) and the Department of Transportation (DOT), contending that the vaccine mandates imposed by these agencies on the airlines’ employees infringed on their constitutional, religious, and medical liberties.
The lawsuit against Atlas Air was filed in federal court in the Southern District of Florida, with over 100 plaintiffs pursuing litigation.
“Fundamentally, this case is about whether Americans should be required to choose between their livelihoods and being coerced into taking an experimental, dangerous medical treatment,” reads the lawsuit (pdf).
Plaintiffs are mostly unvaccinated pilots, flight attendants, as well as other Atlas staff.
VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.
The data included a total of 28,532 reports of deaths — an increase of 220 over the previous week — and 235,041 serious injuries, including deaths, during the same time period — up 2,347 compared with the previous week.
Excluding “foreign reports” to VAERS, 825,454 adverse events, including 13,150 deaths and 83,454 serious injuries, were reported in the U.S. between Dec. 14, 2020, and May 27, 2022.
Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.
Of the 13,150 U.S. deaths reported as of May 27, 16% occurred within 24 hours of vaccination, 20% occurred within 48 hours of vaccination and 59% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.
In the U.S., 586 million COVID-19 vaccine doses had been administered as of May 27, including 346 million doses of Pfizer, 221 million doses of Moderna and 19 million doses of Johnson & Johnson (J&J).
Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.
“Vaccine injury compensation programs overwhelmed by thousands of reports. Federal programs compensating people who suffered injuries from vaccines or COVID-19 pandemic treatment are facing so many claims that thousands of people may not receive payment for their injuries for a long time, Politico reported.“
1.) Defending The Republic Demands The FDAStop Hiding Information From the American Public
Yesterday, Defending the Republic filed suit in a Dallas federal court demanding the FDA stop hiding information from the American public and produce ALL data and records it was provided in approving Moderna’s COVID-19 vaccine.
We have been on the front lines in the fight against unlawful COVID-19 mandates, which were implemented in conjunction with the FDA’s improper approval of the Pfizer and Moderna vaccines.
As more information comes out regarding the safety and effectiveness issues of these vaccines, and as the COVID-19 deaths of the fully vaccinated continue to rise, it is essential that the American public has access to Moderna’s “Spikevax” data.
This latest action by Defending the Republic seeks the expedited production of those records. Through its fights in the courts, Defending the Republic will guarantee the public’s right to review that data for themselves.
2.) Pediatricians are backing off of forcing the Covid-CCP injection on children.
1.) Jody Harris joins Doc Washburn on his show today to discuss the theft of her election in house district 25. Listen at 11AM on his website, or anytime thereafter with your favorite podcast app. http://docwashburnshow.com
2.) Moderna Throwing Away 30 Million Doses of COVID Vaccine Because ‘Nobody Wants Them’
Our betters in the World Economic Forum (WEF) gathered in Davos this week to decide what’s best for the planet and everyone on it (especially themselves). But Stéphane Bancel, CEO of Moderna, was sad. He was disappointed that the plebs don’t want his company’s revered COVID-19 vaccines.
“It’s sad to say, I’m in the process of throwing 30 million doses into the garbage, because nobody wants them,” lamented Bancel as he participated in a panel discussion. “We have a big demand problem.” Actually, that sounds like a big over-supply problem to me, but what do I know?
Bancel elaborated on the outreach efforts the pharma giant was making to “every country,” including going around to all the embassies in Washington, D.C., to entreat governments to distribute the excess shots to their citizens. But sadly, he concluded, “nobody wants to take them.”
“The challenge we have now is [a] very different situation than we had two years ago. The problem we had two years ago is there was no mRNA capacity in the world. Zero.”
“The situation is very different today,” explained Bancel. “Moderna has three billion doses annual capacity, Pfizer has four billion doses, that’s seven billion doses, and the Chinese don’t want the vaccines with mRNA. So if you just take the, just the Chinese population out, you have more than a dose per person, and as we just discussed, the issue in many countries is people don’t want vaccines.
Bancel called out the ugly Americans. “In the U.S., people don’t want vaccines,” he said. “Around the world, we have a lot of people who don’t want the vaccine,” Bancel mourned, before reiterating that the problem was not a “capacity limit.”
