American Trapped in Japan Because Non-Citizen Wife Can’t Enter U.S. Without COVID-19 Vaccine Proof

An American citizen is stuck in Japan because his non-citizen wife can’t enter the U.S. without showing proof of taking the COVID-19 jab.

Kion, a U.S. citizen who’s been in Japan for over 15 years, reached out to activist TexasLindsay to tell his story.

Kion met his wife while studying abroad at a language school in Japan around 2009. “We’ve been married for about 15 years,” he said, “and our visa in Japan runs out next year.”

“I’m a U.S. citizen that’s basically stranded outside of the country because my wife [a non-U.S. citizen] is being refused an immigration visa,” he said, explaining that they had applied “about 3 years ago, at the start of the pandemic hoping the madness would be over by the time we got the immigration visa.”

“I thought that since we were moving back, I should look for jobs in the states, and never expected to be stuck this long,” he added.

Turns out the reason Kion’s wife’s visa is being denied is due to the Biden DHS and CDC’s immigration requirement for LEGAL immigrants to show proof a COVID-19 injection within the last 12 months.

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Ben Franklin’s Anguish: The Origin of the Modern Vaccine Cult

It’s tough to argue with the vast historical literature documenting that smallpox was indeed a dreadful scourge. During the 18th century, the British Colonies in America were repeatedly struck with outbreaks that killed up to 30% of those infected. Within this context, the procedure known as inoculation became an increasingly accepted though extremely controversial practice. Indeed, today’s conflict between vaccine advocates and skeptics strongly resembles the 18th century controversy over smallpox inoculation.

This essay is NOT an attempt to settle the 18th century debate over smallpox inoculation, but to give a striking illustrative example of why inoculation as a practice became the object of such fervent emotion. In the 18th century, smallpox was a common cause of child mortality, and as anyone who has ever lost a child can tell you, the experience is probably the worst thing that can happen to man or woman who has become a parent. Watching a child die of a terrible disease would likely test the religious faith of a saint by raising the question: If God cares about me and my wife, why would he allow our beloved child to suffer a terrible death before our very eyes?Corsi Ph.D., Jerome R.Buy New $21.59(as of 04:44 UTC – Details)

Among the Founding Fathers, Benjamin Franklin probably had the most wide-ranging curiosity and interest in solving practical problems. For most of his adult life, he was haunted by the death of his second son, Francis Folger Franklin. As described in the 2011 New York Times essay, Life, Liberty and the Pursuit of Vaccines, by Howard Markel, MD.

Franky, as his parents called him, was born in 1732 a golden child, his smiles brighter, his babblings more telling and his tricks more magical than all the other infants in the colonies combined. Benjamin advertised for a tutor when the boy was only 2.

When he died of smallpox at age 4, the Franklins were beyond condolence. His tombstone was inscribed, “The delight of all who knew him.”

Rumors abounded that Franky had died from an inoculation gone awry. The gossip led the grieving Franklin to declare that his son had never been inoculated because he was suffering from “flux,” or protracted diarrhea. Franklin insisted that Franky “receiv’d the distemper” smallpox “in the common way of infection…

Following this terrible experience, Franklin became of the most tireless advocates of smallpox inoculation in the colonies.

In their magisterial work of medical history, authors Roman Bystrianyk (Author), Dr. Suzanne Humphries make a compelling case that smallpox inoculation advocates such as Franklin were mistaken in their belief that inoculation was truly safe and beneficial. I suspect it would be very difficult to settle this controversy once and for all, as both the natural infection and the inoculation procedure were ghastly with high rates of mortality.

Nevertheless, it’s easy to understand why Benjamin Franklin would place enormous interest and hope in smallpox inoculation. After all, smallpox was a scourge against which humanity perceived itself to be helpless. As imperfect as it was, inoculation seemed to offer at least some hope. And as we have all experienced when faced with a fearful prospect, doing something to try to improve our odds often strikes us as better than nothing. For many reasonable people, gambling on the inoculation therefore seemed like a risk worth taking.

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Childhood Vaccine Schedule Led to ‘Greatest Decline in Public Health in Human History’

A U.S. Senate roundtable discussion, hosted by Sen. Ron Johnson, tackled a taboo topic — why public health agencies have not studied the health outcomes of vaccinated versus unvaccinated children — and have refused to make data on the topic available to the public.1

“They do not publish the results [or] let any independent scientist in to look at that information,” Brian Hooker, chief scientific officer for Children’s Health Defense, said. “They refuse to publish the results and they really know why. It’s because the bloated vaccination schedule is responsible and is, I would say, in part responsible for the epidemic of chronic disorders that we see in children in the U.S.”2

In 1962, children received just five vaccine doses. As of 2023, children up to age 18 receive 73 doses of 16 different vaccines. The cumulative effects of this childhood vaccine schedule have never been tested.

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‘Indefensible’: Courts finally scrutinize COVID vaccine mandates as religious infringement

Three years after COVID-19 vaccines became widely available to adults – at which point the CDC already knew they couldn’t stop transmission – courts are finally starting to put their foot down on the most basic legal question: Are mandates at least applied fairly, if not scientifically?

The 10th U.S. Circuit Court of Appeals not only knocked down the University of Colorado medical school’s original and revised 2021 mandates for discriminating against employees seeking religious exemptions, but knocked the trial judge for “abuse of discretion” by reversing the burden of proof to moot the case.

The Anschutz campus, whose dental school recently created a diversity, equity and inclusion award, made an early pivotal decision on COVID vaccine mandates by scrutinizing the content as well as sincerity of beliefs among employees and students seeking exemptions.

“The Administration’s September 1 Policy is not neutral on its face; the September 24 Policy is not neutral in practice; and both substantially burden” the religious exercise of the anonymous 11 female and six male plaintiffs, according to the majority opinion by Judge Allison Eid, who replaced Neil Gorsuch when President Trump appointed him to the Supreme Court.

“It is manifestly unreasonable to think” the Sept. 24 policy “would reach precisely the same results … by accident,” Eid wrote. “The Administration had spent weeks or months drafting and implementing a policy hostile toward and discriminatory against certain religions, only to adopt a new, purportedly neutral policy that reached precisely the same results.”

University of California San Francisco epidemiologist Vinay Prasad celebrated the ruling for recognizing CU Anschutz administrators “set an indefensible policy,” while the plaintiffs’ lawyers at the Thomas More Society thanked the court for recognizing the university’s “value judgments … reeked of religious bigotry” and violated constitutional rights and “basic decency.”

The ruling is reminiscent of the Supreme Court’s narrow finding against the Colorado Civil Rights Commission for “official expressions of hostility to religion” when it punished Masterpiece Cakeshop owner Jack Phillips for declining to make custom wedding cakes for gay couples based on his Christian view of marriage.

In the private sector, a high-profile vaccine mandate lawsuit by an actor fired from the Fox show “911” is heading to trial over whether Disney-owned 20th Television trampled Rockmond Dunbar’s views as a follower of the Church of Universal Wisdom, which The New York Times profiled in 2003 for its utility in circumventing childhood vaccination mandates.

“It appears that Disney vetted exemption applications on a case-by-case basis, investigating whether the religions constituted true religious institutions and whether applicants actually followed the beliefs,” according to The Hollywood Reporter.

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How the US Government (FDA, DOD) removed the requirement for informed consent for EUA Countermeasures.

I wanted to add some information to a recent post by Katherine Watt: email answer to Bill Marshall (Judicial Watch). I agree with Katherine that both “approved” Biologics License Approval (BLA) and EUA versions of covid shots are fake and poisonous. This applies to all of the 400+ covid products on the market – all of them are Emergency Use (EUA) only.  The most important thing about EUA status – it is non-investigational by law (Para 564 of FDCA).  Most people do not fully grasp the meaning of this.  While a chemical entity is classed as a non-investigational entity, it can never become a medicinal product in the ethical meaning of medicine, i.e. to treat, deliver some therapeutic benefit while minimizing the risk.  That is completely out of the question for an EUA.  It can never be used in a real clinical trial, because a clinical trial is a legally safeguarded investigation in humans.  Since no clinical trials are possible, no FDA approval (BLA) is possible as BLA by law requires safeguarded clinical trials with informed consent. 

The BLA can only be theoretically achieved if the PHE is terminated, PREP Act declaration is terminated, EUA is revoked, product removed from market, and only after a new set of regulated, safeguarded real clinical trials are performed.  Obviously, this will never happen for mRNA products. Given the well-documented slaughter that they have caused, any institutional review board (IRB) that is insane enough to approve a “trial” of a known lethal poison in humans will have a bullseye painted on it for liability lawsuits. There is no way to ever test this garbage in people under normal ethical bioresearch frameworks. In addition, it is impossible to manufacture these things to cGMP/pharma standards, as making of biologics is a probabilistic and not a deterministic process. All of this was well known to the regulators, DARPA and to manufacturers prior to 2020. That’s why they went into so much effort to change the US law and construct the legal kill box which thoroughly shields them from liability before faking the pandemic, lying on a massive scale and deploying this poison on billions of people.

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DNA Contamination in Pfizer COVID Shot 500 Times Permissible Level: New Study

Genetic impurities in the Pfizer mRNA COVID vaccine could be as high as 500 times the permissible limit, according to a new study.

In the study, published in Methods and Protocols, two German researchers raise worrying questions about the reliability of the quantitative PCR technique used by Pfizer-BioNTech to measure DNA contamination in the vaccine.

Using their own tests on the vaccine’s lipid nanoparticles, they discovered levels that were between 360 and 534 times higher than the 10 nanogram per dose limit set by regulators.

The researchers argued that the methods used by Pfizer-BioNTech test for only 1% of the original DNA template used to make the vaccine, meaning that 99% of the genetical material from the template therefore goes untested and potentially undetected.

Similar concerns have been raised by other researchers.

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Ex-CDC Director Says It’s High Time To Admit ‘Significant Side Effects’ Of COVID-19 Vaccines

Dr. Robert Redfield, former director of the Centers for Disease Control and Prevention (CDC), said Thursday that many officials who tried to warn the public about potential problems with COVID-19 vaccines were pressured into silence and that it’s high time to admit that there were “significant” side effects that made people sick.

Dr. Redfield made the remarks in a May 16 interview with Chris Cuomo on NewsNation, during which he lamented the loss of public confidence in public health agencies because of a lack of transparency around the vaccines, which he said “saved a lot of lives” but also made some people “quite ill.”

Those of us that tried to suggest there may be significant side effects from vaccines … we kind of got canceled because no one wanted to talk about the potential that there was a problem from the vaccines, because they were afraid that that would cause people not to want to get vaccinated,” Dr. Redfield said.

In his role as head of the CDC, Dr. Redfield was part of the Trump administration’s Operation Warp Speed, a project to surge COVID-19 vaccine development at a time during the pandemic when little was known about the virus and rapid vaccine rollout was widely seen as key to getting the outbreak under control and lockdowns lifted.

In September 2020, a few months before the first COVID-19 vaccines were given in the United States, Dr. Redfield testified before the Senate that COVID-19 represented the “most significant public health challenge to face our nation in more than a century,” and that the prevailing view among scientists at the time was that the overall case fatality rate of the disease was somewhere between 0.4 and 0.6 percent in the United States.

If you were to look right now, individuals under the age of 18, it’s about 0.01 percent, 19 to say 69, it’s more like 0.3 percent. And if you’re over the age of 70, it’s about 5 percent now,” he testified at the time.

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Further Ethical Concerns on a Recent Self-Amplifying RNA Vaccine Study

I called for the ongoing study to be ceased given the mass safety signal pointed out by The McCullough Foundation.

Today, I outline further ethical flaws:

  1. Informed Consent:
  • Participants must be fully informed about the novel nature of srRNA technology, including potential unknown long-term effects. Ensuring that informed consent is genuinely informed is critical.
  • Detailed information about the potential risks and benefits, including those observed in preclinical and early-phase clinical trials, should be provided.
  • Since the long-term risks are unknown, this seems impossible.
  1. Conflict of Interest:
  • The authors are employees of Replicate Bioscience Inc., which raises concerns about bias. The review should disclose how the conflict of interest was managed.
  • Independent oversight or review by third-party experts who do not stand to benefit financially from the vaccine should be conducted.
  1. Safety Monitoring:
  • Continuous monitoring for adverse effects is essential, especially given the novel nature of srRNA vectors.
  • Clear protocols for reporting and managing adverse events, including long-term follow-up, and plans to mitigate the ill-health effects of AEs and SAEs, must be transparent and outlined up-front.
  1. Methodological Issues

Cause of Death Determination:

  • Accurate determination of causes of death in clinical trials is crucial. There should be a standardized protocol for post-mortem analysis to ascertain whether deaths are related to the vaccine or underlying conditions. Doctors working for the company determining that the vaccine was not the cause of death is insufficient: it’s a novel vaccine: how do they know they are not confusing deaths from COVID19 with deaths from vaccines? PCR is known to be fraught with errors in this context. How do they know that the vaccine does not interact with COVID19 infection and increase mortality?
  • Independent medical reviews of cause-of-death determinations can mitigate bias.

Manufacturing Quality:

  • The article mentions impurities from poor manufacturing that lead to systemic inflammatory responses. To minimize such risks, strict quality control measures and validation processes should be in place.
  • Detailed documentation and transparency regarding manufacturing practices are essential to ensure reproducibility and safety.

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Pfizer’s Covid Gene Therapy Shots Have Over 500 Times Allowable Levels of DNA Contamination — Study

study published this month has found that the Pfizer mRNA Covid ‘vaccine’ gene therapy injections contain DNA contamination at over 500 times allowable levels, raising fears that the DNA may integrate into the vaccinated person’s own DNA, causing mutations that can lead to diseases such as cancer.

“The available information and data indicate that the ready-to-use mRNA vaccine Comirnaty contains DNA impurities that exceed the permitted limit value by several hundred times and, in some cases, even more than 500 times,” the study said in the ‘Conclusions’ section.

Modified messenger RNA (mRNA) vaccines work by encapsulating the RNA sequence of the Covid spike protein (the dangerous part of Covid, linked to HIV) into lipid nanoparticles which are able to deliver the RNA payload into the body’s cells. The RNA is then integrated into the person’s genetics so they will produce the Covid spike protein, which the body can then develop an immune response to.

However, according to the study, mRNA is not the only genetic information being injected into people.

“…in addition to the mRNA active ingredient, DNA impurities are also encased in lipid nanoparticles and are therefore difficult to quantify,” the study said in the ‘Abstract’ section.

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Marathon Runner Left Disabled By AstraZeneca Covid Jab Now Suing Company, But UK Taxpayers To Foot Bill

A 50-year-old UK man named Adrian Walker was left disabled after taking the AstraZeneca Covid shot, and now he’s part of a class-action lawsuit against the company.

This comes as the pharmaceutical giant takes its COVID-19 jab off the market worldwide due to health hazards.

However, even if the 51 people pursuing legal action against the company are successful in court, AstraZeneca will be financially off the hook as the UK government gave the company legal immunity during the pandemic.

Because of the government’s deal with AstraZeneca, and other Covid jab manufacturers, UK taxpayers will instead foot the bill.

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