Tag: body integrity

Gov. DeSantis Seeks Permanent Ban On mRNA Vaccine Mandates And Other Restrictions

Florida Governor Ron DeSantis and his wife Casey have called on the Centers for Disease Control and Prevention (CDC) to stop recommending the COVID-19 vaccine for children, as well as for the state legislature to permanently prohibit mRNA mandates and to add vaccination status protections to the Patient’s Bill of Rights. 

“Guided by common sense and sound science, Florida has led the way in protecting patients’ rights. Now is the time to secure these protections and do even more to defend medical freedom,” said DeSantis (R-Fla.). “Let’s keep Florida the beacon of freedom in health care, where the rights of all patients are enshrined permanently in law.”

“Today, Governor DeSantis, Surgeon General Ladapo, and I called on the Florida Legislature to make permanent the prohibitions against the COVID mRNA vaccine mandate,” said First Lady Casey DeSantis. “Florida stood in the breach to protect people during COVID, now it’s time to make sure these protections last.”

“I am deeply grateful to Governor Ron and First Lady Casey DeSantis for continuing to put the needs and rights of Floridians first,” said State Surgeon General Dr. Joseph A. Ladapo. “These proposals will strengthen the sovereignty of patients, and we look forward to advancing these issues with our federal partners at the U.S. Department of Health and Human Services.”

The call to ban mRNA vaccine mandates by DeSantis is a law that already exists in the Sunshine State but is set to expire in June. 

DeSantis said he has no idea why the Legislature added an expiration date in the bill, but he is calling on lawmakers to extend the ban and make it permanent.

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Ohio veteran calls for change after being denied heart transplant over vaccine refusal

Ken Long, a 54-year-old veteran from Eaton, has been denied a heart transplant at Christ Hospital due to his refusal to receive the COVID-19 vaccine.

Long, who was diagnosed with congestive heart failure nearly a year ago, believes the decision is based on his vaccination status.

“When I decide something, I mean it, and if it takes dying, it’s what it is,” Long said. “They don’t know enough about it, and plus it’s already done a lot of damage. People have said blood clots. There are no cardiac issues and our personal religious rights.”

Initially, Long’s wife, Christina, disagreed with his decision.

“It’s my husband. I don’t want to lose my husband,” Christina said. “In the moment, you’re just overwhelmed, and you want to do anything you can to save somebody’s life, and then I had to regroup myself. It’s his right.”

Long now relies on a left ventricular assist device (LVAD) to pump blood to his heart.

“I can hardly do anything. If the power goes out, I have to worry about my batteries and my charger,” Long said. “You can’t get wet, so showering is an issue.”

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Ontario school children face compelled medical surveillance or suspension

Ontario school children are currently caught in the middle of an ongoing issue regarding student rights, medical privacy, and the power of public health authorities. Under the Immunization of School Pupils Act (ISPA), students attending Ontario schools are required to be vaccinated against certain diseases unless exempt for medical, religious, or philosophical reasons.

However, the recent push by public health officials to have students disclose their vaccination status and face suspension for non-compliance is raising serious privacy concerns.

The problem lies in the ambiguity between ISPA and the Education Act. ISPA stipulates vaccine requirements, but suspension orders are the responsibility of school principals under the Education Act, not public health authorities. This confusion is leading to violations of students’ fundamental right to a free public education, with some students at risk of being unlawfully suspended for failing to disclose their vaccination status.

The pressure to disclose private medical information is causing significant distress among parents and children alike. There are increasing concerns about the safety of centralized digital health databases, which have been vulnerable to data breaches and unauthorized access. With healthcare data a prime target for cyberattacks, parents are understandably worried about the security of their children’s sensitive medical records—which is big business for hackers.

Parents are resisting this growing pressure, with some viewing the disclosure demands as a violation of the Personal Health Information Protection Act (PHIPA). PHIPA requires informed consent before the collection of medical information and protects against coercion. However, the current approach by threatening suspension or else puts this principle into question.

The Ministry of Education was contacted for clarification, but media representatives Ingrid Anderson and Brook Campbell failed to respond days later. The inquiry focused on the confusion between ISPA and the Education Act, and how these conflicting laws are affecting students’ right to education. Additionally, clarification was sought on how medical privacy is being protected for parents wishing to uphold PHIPA.

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The Compromised FDA Knows Exactly What It’s Doing

The sneaky bastards at the FDA did this a year ago, right under our noses. In January 2024, the FDA finalized a rule permitting Institutional Review Boards (IRBs) to waive or even alter informed consent requirements for clinical investigations deemed “minimal risk.” TTR guest author Jon Fleetwood, as always, brings us this news in his excellent reporting. Read his entire article here.

IRBs. Informed Consent. What does it all mean? If you don’t do research, you likely won’t know.

What is an IRB?

An Institutional Review Board (IRB) is a panel of individuals who review and oversee research studies that involve human participants. The IRB ensures that the studies are ethical and that they comply with all regulations. The IRB’s primary function is to protect the rights and welfare of the human research participants, making sure they are treated fairly, ethically and safely.

Anyone doing research must have an IRB, and that not only applies to direct human research (meaning the human is actually being given a drug or using a device), but also for indirect studies where the patient isn’t “touched” so to speak or actively involved. A direct example would be a clinical trial where a new drug is being tested. The human participants actually enroll in the trial and are given test doses of the medication. Even if a human participant is given a placebo, that research must be covered by an IRB to ensure the patients’ physical and psychological well-being. An example of an indirect study is one in which a company or other research entity is just using data from patients, with no direct patient interaction. In some cases an IRB is still needed to use data that may potentially identify who the subjects are.

The bottom line is that an IRB is needed for any drug, device assessment, survey or other study. And this is what makes the FDA’s ruling so unbelievable. Fleetwood says the implications are staggering, and he is absolutely right:

“Under this waiver, any person’s health data, biospecimens (such as blood or tissue samples), or medical records can be accessed and used for FDA-regulated research if it meets vague and highly subjective criteria.”

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Drones Spray ‘Self-Spreading’ COVID-19 Vaccine for ‘Large-Area Inoculation of Humans’ in ‘DEFUSE’ EcoHealth/DARPA Project

  • EcoHealth’s DEFUSE Proposal Exposed: In 2018, EcoHealth Alliance submitted a proposal to DARPA, codenamed DEFUSE, outlining plans to deploy aerosolized immune modulators, chimeric spike proteins, and/or self-spreading vaccines via drones, potentially over humans.
  • Aerosolized Vaccination on Humans: DEFUSE documents explicitly describe large-area aerosol delivery systems for “inoculation of animals/humans,” raising the question of whether these plans were executed on unsuspecting populations.
  • Drone Deployment and Pandemic Origin: The DEFUSE proposal and DARPA’s advanced drone programs suggest a chilling possibility: that drones may have played a role in the COVID-19 pandemic, challenging the mainstream lab-leak narrative.
  • DARPA’s Connection to Moderna: By 2012, DARPA was already working with Moderna on RNA-based spike protein vaccines. A 2016 Moderna patent contains a genetic sequence with a one-in-3-trillion match to the pandemic virus, igniting claims of bioengineering origins.
  • Suppression of DEFUSE Details: Whistleblower revelations show attempts by DARPA and intelligence agencies to classify and censor DEFUSE-related research. U.S. senators have demanded investigations into these actions.
  • Self-Spreading Vaccines and Gain-of-Function: DEFUSE documents reveal plans for self-disseminating vaccines and host-to-host therapeutic distribution, indicating the potential use of engineered viruses as vaccine delivery systems.
  • Unprecedented Drone Funding Surge: A 26% spike in military drone funding in 2019 aligns with DEFUSE’s timeline and its drone-based aerosol delivery technologies, hinting at pre-pandemic preparations.
  • International Drone Use During COVID-19: Governments worldwide deployed drones for “disinfecting,” but studies debunk the effectiveness of this practice, raising suspicion about the true purpose of these operations.
  • A Coordinated Bioengineering Agenda?: The alignment of DEFUSE, DARPA, and drone advancements reveals an unsettling intersection of gain-of-function research, bioweaponized delivery systems, and self-spreading vaccines.
  • Urgent Transparency Needed: The DEFUSE project raises alarming questions about the origins of COVID-19, the ethics of aerosolized bioengineering, and the U.S. government’s role in these developments. The public deserves truth and accountability, especially considering a potentially incoming bird flu pandemic.

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Vermont Supreme Court Ruling Allows Schools to Administer COVID Vaccines Without Parents’ Consent

Numerous mainstream media outlets are deliberately lying to American parents about the law regarding COVID-19 vaccines.

In August, Vermont’s Supreme Court that ruled a 6-year-old boy administered a COVID-19 vaccine against his parents’ specific instructions that he not be jabbed has no state tort remedies, and that the family’s sole recourse is a federal claim requiring proof of serious bodily harm or death to proceed.

All other traditional causes of action for violating these parents’ rights, and fundamental constitutional informed consent protections for patients, are extinguished completely. And yet, numerous media outlets reported the precise opposite. This is blatant misinformation.

The Associated Press (AP) launched an utter deception titled falsely: “Fact Focus: Vermont ruling does not say schools can vaccinate children without parental consent.” This is the opposite of the truth: Politella v. Windham Southeast School District, et al. held exactly that:

“Other state courts faced with similar facts have concluded that state-law claims against immunized defendants cannot proceed in state court in light of the PREP Act’s immunity and preemption provisions, including claims based on the failure to secure parental consent.”

In support of its abject lie, the AP cited a Vermont Law School professor:

“Rod Smolla, president of the Vermont Law and Graduate School and an expert on constitutional law, told The Associated Press that the ruling ‘merely holds that the federal statute at issue, the PREP Act, preempts state lawsuits in cases in which officials mistakenly administer a vaccination without consent.’

“‘Nothing in the Vermont Supreme Court opinion states that school officials can vaccinate a child against the instructions of the parent,’ he wrote in an email.”

Professor Smolla is an embarrassment to the Vermont Law School of which he is President. Politella specifically holds that all state tort claims, including those alleging willful jabbing, are preempted by federal law.

In observable fact, the court ruled that the Politella family could not proceed with their case — even though the complaint alleges that the school “vaccinated a child against the instructions of the parent.” Where did professor Smolla not learn the law? — a 6-year-old can read the case and see the falsehood of his statement.

The Politella court specifically determined that “each defendant is immune from plaintiffs’ state-law claims, all of which are causally related to the administration of the vaccine to [the minor child] L.P.”

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PREP Act Empowers Gov’t to ‘Administer’ Drugs, Biological Products, Devices to Citizens in Secret

Big Picture: The Public Readiness and Emergency Preparedness (PREP) Act, codified at 42 U.S. Code § 247d–6d, grants the government extraordinary authority to deploy countermeasures during public health emergencies. These powers allow for sweeping actions that include administering drugs, devices, or biological products to populations—without requiring public knowledge or consent. Signed into law by President George W. Bush on December 30, 2005, as part of the Department of Defense appropriations bill (H.R. 2863), the PREP Act was intended to prepare the nation for biological threats but has since raised questions about accountability and transparency.

Focus: The PREP Act’s language reveals how liability immunity, broad discretion for the Secretary of Health and Human Services (HHS), and exemptions from disclosure requirements create an alarming framework for secretive government actions.

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Patients Unknowingly Received Covid Jabs While Under Sedation at Hospitals, US Attorneys Claim

Patients at local hospitals were unknowingly given Covid vaccinations while under sedation, a group of lawyers has claimed.

According to the Freedom Counsel, which defends victims who were affected by the jab and mandates, they’ve received multiple accounts of people who claim they were injected with the experimental mRNA jab while under anesthesia for other medical procedures.

“Were you or a family member covid vaxxed while under sedation? We are hearing stories of this abominable covert act,” Freedom Counsel founder Warner Mendenhall wrote on X earlier this month.

Mendenhall went on to say he’s verified the accounts through health care workers, adding that many patients wouldn’t know if they were jabbed under sedation because it was probably not documented on charts.

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Parents Appeal To U.S. Supreme Court After Vermont Courts Ruled Schools Can Vaccinate Kids Against Parents’ Wishes

A Vermont family whose 6-year-old son was vaccinated with an experimental Covid-19 intervention against the family’s wishes has appealed a Vermont Supreme Court ruling. The Vermont court had ruled that the Public Readiness and Emergency Preparedness Act (PREP) prohibits such claims, granting immunity to school and government personnel when they mandate vaccinations.    

Stunningly, the Vermont Supreme Court did not even pay lip service to the constitutional liberties implicated, ruling against traditional protections of parental rights and informed consent. But the PREP Act is not above the Constitution’s supremacy clause; it’s the other way around.      

Parents’ rights are being chiseled away rapidly. In Vermont, minor children may obtain transgender hormones and birth control without parental consent, and a 2024 law bars parents from seeing which library books are checked out by their children 12 years and older. Yet these are examples where the child wants something against his parents’ wishes. In Vermont’s Covid-19 vaccination case, the child protested and was forced to be jabbed anyway.

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Kamala Harris Opposes Informed Consent to Vaccinations

Kamala Harris, the Democratic Party’s presidential candidate and the current Vice President under the Joe Biden administration, previously served as Attorney General for the state government of California, during which time she served the financial interests of pharmaceutical industry.

For that reason, she makes an appearance in my 2021 book The War on Informed Consent: The Persecution of Dr. Paul Thomas by the Oregon Medical Board.

Here’s the relevant excerpt:

Paul Thomas’s approach of grounding his practice in the principle of informed consent and focusing on health outcomes stands in stark contrast to the approach taken by the state government of violating informed consent to achieve high vaccination rates.

Oregon, of course, is not alone. All the states have taken the approach of mandating vaccinations for school attendance. In the extremity of its coercion, Oregon was outdone by California, which in 2016 passed a law eliminating “non-medical” exemptions.

However, that did not have the intended effect because it incentivized parents to go to pediatricians who are respectful of informed consent to obtain a medical exemption. The problem, as perceived by those myopically focused on achieving high vaccination rates, was that physicians might grant exemptions “for indications outside of accepted contraindications”, such as on the basis of “family medical history”.

The law was considered to “work” not based on whether it achieved a healthier childhood population but whether it increased the childhood vaccination rate. Pediatricians who would write medical exemptions for reasons such as the patient having a family history of autoimmune disease were regarded as “accomplices”—as though by enabling parents to exercise their right to informed consent they were engaging in criminal activity.

The state Senator who spearheaded the elimination of “non-medical” exemptions, Dr. Richard Pan, subsequently introduced a bill he described as being intended strengthen “oversight” of physicians to stop them from writing “fake” medical exemptions, which were those found by the state “to be fraudulent or inconsistent with contraindications to vaccination per CDC guidelines.” (Emphasis added.)

With the passage of that bill into law in September 2019, the state declared for itself the authority to revoke medical exemptions written by licensed physicians, with the clear warning communicated to doctors that if they write exemptions for any reasons other than CDC-defined contraindications, the state was going to come after them for their “unscrupulous” behavior.

Richard Pan expressed his view on the matter very clearly in a commentary in the AAP’s journal Pediatrics. When physicians write medical exemptions to state vaccine mandates, he wrote, it is “not the practice of medicine but of a state authority to licensed physicians” who are “fulfilling an administrative role” on behalf of the state.

Thus, in Pan’s view, the state’s proper role is to insert itself into the doctor-patient relationship by dictating how pediatricians should practice medicine, and informed consent for the parents is not an option.

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