More Medical Studies Needed Explore Dr. Paul Thomas’ Findings Regarding Vaccination

Dr. Paul Thomas gathered data from his patients over many years. 2,700 vaccinated and 560 unvaccinated. You can see Dr. Paul's data here.. He explains his findings below. I have no expertise in this area and I am not making any medical claims, except for this: This data is disturbing, arguably terrifying. More studies are needed to confirm or dispel Dr. Paul's findings and concerns.

I gathered information from 2,700+ vaccinated children and 500+ unvaccinated children in MY OWN CLINIC. The findings are remarkable: asthma, allergic rhinitis, eczema, sinusitis, gastroenteritis, respiratory infections, behavioral issues, ADD, ADHD, conjunctivitis, and breathing issues are all SIGNIFICANTLY WORSE in the #Vaccinated children.

Wait a minute, I thought that vaccines were supposed to prevent infections. What's going on here?"

Also, he shares an eye-opening observation: "In my 10 years of practice, I have had ZERO kids with ADHD that were unvaccinated! That's UNBELIEVABLE, folks!" - Do you know that NO AMISH person has ever been diagnosed with ADD or ADHD? What do the Amish and unvaccinated children have in common?

Wouldn’t it be beneficial to further understand the potential implications on the health of children who receive childhood vaccines? It seems like a NO-BRAINER to me

Continue ReadingMore Medical Studies Needed Explore Dr. Paul Thomas’ Findings Regarding Vaccination

A Review of Some of the Amicus Briefs Filed in the U.S. Supreme Court Case of Murthy v Missouri

Murthy v Missouri will be argued on March 18. This is one of the most important First Amendment cases in this history of the U.S. Supreme Court, yet A) the NYT and most other big corporate news outlets will not discuss it and B) the ACLU refuses to get involved.

On his Substack, Aaron Kheriaty, M.D., discussed some of the amicus briefs filed in a nationally important in which he is a plaintiff, Murthy v Missouri (called Missouri v Biden in lower courts).

How important is this case?  Here is an excerpt from the opinion of the Fifth Circuit Court of Appeals:

We find that the White House, acting in concert with the Surgeon General’s office, likely (1) coerced the platforms to make their moderation decisions by way of intimidating messages and threats of adverse consequences, and (2) significantly encouraged the platforms’ decisions by commandeering their decision-making processes, both in violation of the First Amendment...

Generally speaking, officials from the White House and the Surgeon General’s office had extensive, organized communications with platforms. They met regularly, traded information and reports, and worked together on a wide range of efforts. That working relationship was, at times, sweeping. Still, those facts alone likely are not problematic from a First-Amendment perspective. But, the relationship between the officials and the platforms went beyond that. In their communications with the platforms, the officials went beyond advocating for policies ... or making no-strings-attached requests to moderate content ...Their interaction was “something more.”

We start with coercion. On multiple occasions, the officials coerced the platforms into direct action via urgent, uncompromising demands to moderate content. Privately, the officials were not shy in their requests they asked the platforms to remove posts “ASAP” and accounts “immediately,” and to “slow[]down” or “demote[]” content. In doing so, the officials were persistent and angry. Cf. Bantam Books, 372 U.S. at 62–63. When the platforms did not comply, officials followed up by asking why posts were “still up,” stating (1) “how does something like [this] happen,” (2) “what good is” flagging if it did not result in content moderation, (3) “I don’t know why you guys can’t figure this out,” and (4) “you are hiding the ball,” while demanding “assurances” that posts were being taken down. And, more importantly, the officials threatened—both expressly and implicitly—to retaliate against inaction. Officials threw out the prospect of legal reforms and enforcement actions while subtly insinuating it would be in the platforms’ best interests to comply. As one official put it, “removing bad information” is “one of the easy, low-bar things you guys [can] do to make people like me”—that is, White House officials—“think you’re taking action.”

That alone may be enough for us to find coercion. Like in Bantam Books, the officials here set about to force the platforms to remove metaphorical books from their shelves. It is uncontested that, between the White House and the Surgeon General’s office, government officials asked the platforms to remove undesirable posts and users from their platforms, sent follow-up messages of condemnation when they did not, and publicly called on the platforms to act. When the officials’ demands were not met, the platforms received promises of legal regime changes, enforcement actions, and other unspoken threats. That was likely coercive...

We also find that the FBI likely significantly encouraged the platforms to moderate content by entangling themselves in the platforms’ decision making processes.... Beyond taking down posts, the platforms also changed their terms of service in concert with recommendations from the FBI. For example, several platforms “adjusted” their moderation policies to capture “hack-and-leak” content after the FBI asked them to do so (and followed up on that request). Consequently, when the platforms subsequently moderated content that violated their newly modified terms of service (e.g., the results of hack-and-leaks), they did not do so via independent standards.... Instead, those decisions were made subject to commandeered moderation policies. In short, when the platforms acted, they did so in response to the FBI’s inherent authority and based on internal policies influenced by FBI officials. Taking those facts together, we find the platforms’ decisions were significantly encouraged and coerced by the FBI...

[T]he Supreme Court has rarely been faced with a coordinated campaign of this magnitude orchestrated by federal officials that jeopardized a fundamental aspect of American life. Therefore, the district court was correct in its assessment—“unrelenting pressure” from certain government officials likely “had the intended result of suppressing millions of protected free speech postings by American citizens.”

State v. Biden, 80 F.4th 641, 653 (5th Cir.), opinion withdrawn and superseded on reh'g, 83 F.4th 350 (5th Cir. 2023), cert. granted sub nom. Murthy v. Missouri, 144 S. Ct. 7 (2023).

Based on Kheriaty's summaries of the amicus briefs, it's surreal to see how many formerly admirable institutions have become throughly corrupted by money (often government money) and power to represent the joint position of the U.S. Government and mega-corporations. This is what you might expect with so many entities receiving government largess to do the government's dirty work. This includes the ACLU, as Kheriaty comments:

Not long ago, the ACLU would have championed the plaintiffs in Missouri v. Biden. The organization was founded in 1920 in response to the Wilson administration criminalization of dissent regarding World War I. After the jailings of journalists, pamphleteers, and presidential candidate Eugene Debs, the ACLU immediately began defending anti-war activists’ First Amendment freedoms.

The ACLU famously defended neo-Nazis’ right to march through a Jewish suburb, but the organization later became an arm of the Democratic Party, shedding its former principles in the process.

The group has no shortage of amici briefs and opinions on their website; they’ve petitioned courts to support gun control, abortion, Covid vaccine mandates, and race-based university admissions and to oppose bans on men in women’s sports and efforts to curb illegal immigration. Despite this flurry of opinions and news releases, the ACLU has not made a single mention of Murthy v. Missouri (or Missouri v. Biden) on its website.

While the politicization of the ACLU has been well-documented over the last decade, it remains remarkable that the country’s most prominent civil liberties organization has decided not to support plaintiffs in what may amount to the most consequential First Amendment case of the last half-century.

This case is coming up for oral argument on March 18.

You wouldn't know much about this based on the silence of corporate media. Kheriaty mentions this:

While news outlets like the New York Times have largely ignored the case and others like CNN have insisted that “it is far from clear that the administration’s conduct amounted to censorship,” the Wall Street Journal has dutifully covered the legal proceedings and taken an editorial stand against the White House’s attacks on free expression.

For a detailed and principled view of Murthy and the First Amendment, consider this amicus brief filed by the Foundation for Individual Rights and Expression.

Continue ReadingA Review of Some of the Amicus Briefs Filed in the U.S. Supreme Court Case of Murthy v Missouri

The Inconvenient Recent COVID Data of the VAERS System

Now that signals are pouring in on the VAERS system (Vaccine Adverse Event Reporting System) that the COVID vaccinations are temporally associated with deaths and injuries, the Gates Foundation shows up right on schedule to attack the integrity of VAERS, warning of "Misinformation and the Vaccine Adverse Event Reporting System."

Dr. Peter McCullough explains his concerns:

Every week in clinic I make entries into the US CDC Vaccine Adverse Event Reporting System (VAERS) as I catch up on years of injuries, disabilities, and deaths that have occurred after vaccination. Because federal fines and penalties are severe for false reporting, I only enter cases in which I have the vaccine card, the full clinical vignette, and my clinical impression that the vaccine either directly caused the problem or significantly contributed in the causal pathway to the new disease or injury suffered by the patient. I did a PUBMED search today and there are > 500 papers that have relied on VAERS for epidemiologic studies of vaccine side effects including death in 126 manuscripts.

As the data mount, it should come at no surprise that the Gates Foundation, a major player in the Bio-Pharmaceutical Complex has come out with an attack on the integrity of VAERS. It came through a JAMA editorial from Kathleen Hall Jamieson, PhD, that implied VAERS is “misinformation” in the title uses the adjective “unverified.” Nothing could be further from the truth. Jamieson, whose Annenberg Center is funded in part by the Bill and Melinda Gates Foundation, goes on to propose a name change to VAERS to further diminish its importance. . . I expect at some moment, the data on vaccine safety will be so overwhelming in VAERS that the CDC will simply shut down access the system for queries and research. As sponsors of the program, the agency will refuse to tell America or the world anything on the safety of the novel, genetic biological products.

For the record, U.S. public health officials have used and trusted the VAERS system for decades. From the current VAERS About Page:

About VAERS

Background and Public Health Importance

Medical professionals working with vaccines Established in 1990, the Vaccine Adverse Event Reporting System (VAERS) is a national early warning system to detect possible safety problems in U.S.-licensed vaccines. VAERS is co-managed by the Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA). VAERS accepts and analyzes reports of adverse events (possible side effects) after a person has received a vaccination. Anyone can report an adverse event to VAERS. Healthcare professionals are required to report certain adverse events and vaccine manufacturers are required to report all adverse events that come to their attention.

VAERS is a passive reporting system, meaning it relies on individuals to send in reports of their experiences to CDC and FDA. VAERS is not designed to determine if a vaccine caused a health problem, but is especially useful for detecting unusual or unexpected patterns of adverse event reporting that might indicate a possible safety problem with a vaccine. This way, VAERS can provide CDC and FDA with valuable information that additional work and evaluation is necessary to further assess a possible safety concern.

Let's see whether this self-description of VAERS, or even fundamental aspects of the VAERS system, changes in response to new suspicious pressures . . .

Continue ReadingThe Inconvenient Recent COVID Data of the VAERS System

COVID Disinformation, Lies and Censorship Explored in Congressional Hearing

Here are at least a dozen major issues relating to COVID that corporate media outlets are actively refusing to discuss. The US govt has actively worked to keep you from discussing these issues on social media. I don't claim to know the answers, but I desperately want to hear these topics vigorously discussed.

Continue ReadingCOVID Disinformation, Lies and Censorship Explored in Congressional Hearing

Robert Malone Analyzes a Self-Serving “Limited Hangout” Regarding mRNA

Robert Malone offers this definition of "limited hangout":

A limited hangout is a propaganda technique of displaying a subset of the available information. It involves deliberately revealing some information to try to confuse and/or prevent discovery of other information.

It misdirects an incautious audience, because information needs a context for correct interpretation. Subtly omitting information changes the interpretation of the surrounding information.

A modified limited hangout goes further by slightly changing the information disclosed. Commercially-controlled media is often a form of limited hangout, although it often also modifies information and so can represent a modified limited hangout.

Why is this important? Because "limited hangouts" are ubiquitous these days. They are a common tactic of those who use propaganda and censorship to create false consensuses and prevent robust national discussion of critically important national issues. When they are caught red-handed, they offer only a tiny subset of information, which has the psychological effect of satiating the audience, causing use to think that the full story has been disclosed. The cleverly disclose a tiny part of what is often their own misconduct and complicity in order to gain just enough credibility that they can they use that ill-gained credibility as a trojan horse for the next chapters of their misconduct.

Robert Malone takes a look at a very credible and scholarly-looking article, identifying it as a limited hangout, point by point. Here's the article:

“Lipid nanoparticle structural components, production methods, route of administration and proteins produced from complexed mRNAs all present toxicity concerns.”

Bitounis, D. et al. Strategies to reduce the risks of mRNA drug and vaccine toxicity. Nat Rev Drug Discov. 23 January 2024. https://doi.org/10.1038/s41573-023-00859-3; PMID: 38263456

Here is an excerpt from Malone's article, his take-away
In this recent review article (23 January, 2024), Bitounis et al. provide a partial disclosure and examination of known risks and toxicities associated with the modified messenger ribonucleic acid/lipid nanoparticle pharmaceutical delivery platform. In general, what makes this publication particularly remarkable is that (collectively) the authors have significant employment or other ties to Moderna therapeutics, a pharmaceutical company whose very name (MODified RNA) indicates its corporate dependency on the feasibility of this technology. As a veteran of prior biopharmaceutical corporations, it is inconceivable to me that these authors do not have pre-existing restrictive non-disclosure agreements with Moderna, and therefore it is highly likely that Moderna pre-approved this publication.

Therefore, my most generous interpretation of the overall intent of the article is that this article summarizes and represents information concerning risks and toxicities of this platform technology which Moderna wishes to have disclosed in a manner which puts the firm, its activities and the underlying platform technology in the best possible light. A less generous interpretation of intent is that this article represents a subtle form of propaganda strategy commonly referred to as a limited hangout.

The essay includes extensive speculation concerning how emerging new technologies such as artificial intelligence and organoids (simplified tissue culture structures mimicking an organ, that are derived from stem cells), as well as well established ‘high tech” approaches such as single cell sequencing can be used to minimize animal model use (a specific NIH objective). They are intended to facilitate more efficient pharmaceutical development and toxicologic analysis of modified-mRNA drug and vaccine development technologies.

Through the jaded eyes of this highly experienced proposal reviewer, this mostly reads like a forward looking justification for increased investment in a variety of expensive new pharmaco-toxicology infrastructure advances which would be in the financial and professional interest of the authors, while avoiding and overlooking time tested approaches to characterizing the profound and wide ranging toxicities of these pharmaceutical preparations.

In other words, this reads as an extended justification for spending a lot of money on new goodies for pharmacologists and toxicologists while avoiding the obvious and less sexy basics that still have yet to be performed and reported.

I highly recommend reading Malone's point-by-point analysis to understand how a limited hangout functions.

Continue ReadingRobert Malone Analyzes a Self-Serving “Limited Hangout” Regarding mRNA