Aletho News

ΑΛΗΘΩΣ

Repeal the National Childhood Vaccine Act of 1986

Good products do not need universal liability shields, but bad actors are enabled by them.

el gato malo – bad cattitude – october 22, 2022

much as been made about the possibility of schools mandating covid vaccinations for kids to be allowed to attend.

it may or may not happen. perhaps it will be treated like a flu shot. perhaps they’ll try for requirements. it’s likely to vary place to place and many states are already saying “no way” and if imposed this could cause flood of school change and really unleash the idea of vouchers and free choice and a swansong for public schools.

in the end, i’m not sure how many are crazy enough to try it and honestly, i doubt that any public school system in america could survive for long mandating this.

i doubt that this is really what the approval is about.

it’s about the liability shield and the subsidies.

and that is a thing we need to fix.

longtime gatopal™ jennifer cabrera has a simple, common sense solution:

If the predicted red wave produces a strong Republican majority in Congress, one of their first acts should be to repeal the National Childhood Vaccine Injury Act of 1986. No excuses, Republicans. Liability is the only mechanism that can produce safe vaccines.

because this law is an abomination.

it creates ALL the wrong incentives and has swollen the US pediatric vaccine schedule (which used to be 3 well tested vaxxes, MMR, DTP, polio) with ineffective or marginally effective crap lacking valid risk reward and possessing meaningful side effect tails.

the case for several (HPV, flu, rota, pneumococcal) is basically non-extant.

but hey, no liability, no need to worry.

interestingly, gardasil does not appear to have this coverage hence the mass of lawsuits.

stop me if this sounds familiar:

landing in court on this is not, perhaps “the system working” as this vaccine looks to have been approved and marketed on numerous false pretenses and perhaps outright fraud. but at least the system is cleaning up its mess after the fact and discouraging such behavior in the future.

and the covid vaccines put all the others in the shade in terms of corners cut and data looking dodgy. but if we shield them and other things like them from liability, where is the disincentive to act badly? (and if you just said “because the drug companies wouldn’t lie to us!” i have some denver harbor bonds to sell you.)

you can get around this exemption by pfinding phraud, but should this really be necessary (especially when they hide the data and thus could have all sorts of little gems in it that the public had not seen)?

so how about we end this harmful “safe harbor” instead?

there is NO good consumer protection reason for this act. it’s a license for pharma to misbehave and it eliminates accountability and incentive to test properly. if you want to jab your drugs into kids, you need to own the side effects.

if you fail to predict or disclose risks, you own the ill outcomes instantly and forever.

let them decide, on that basis, how many studies to do and for how long prior to release.

i would LOVE to see what a class action jury award for fraud in a child vaccine lawsuit looks like.

this is the reason we have a tort system.

let it work.

it’s really simple:

either get voluntary informed consent risk waivers or stop mandating drugs.

mandate + no liability = disaster and “soft mandates” are just as bad.

everyone passes the buck to claim “iT wUZ nEvER a MAnDatE!” when they know full well that it functionally was.

how many times did you see this?

you mandate, you own the side effects. simple, reasonable, and incentive aligning.

this is one we can easily do.

we made this law. it has had perverse, anti-consumer effects. so let’s unmake it.

no more liability waivers.

only voluntary informed consent to risk subject to strict disclosure liability. “oh, we never tested for that!” is no longer an excuse.

i am not saying you get to sue for any bad outcome. but if the risks were not disclosed or were misstated you can. if they did not look for fear of what might be found, they own that. the onus is on them to prove safety and delineate risks and share them accurately and completely.

this encourages full, accurate reporting so people can make real, informed decisions.

it’s kind of stunning that we don’t have this.

if any public agency requires a jab, they become liable for bad outcomes.

no one gets forced and drug companies need to make a case for risk reward that will convince people and providers of healthcare.

let the market find the proper level of testing and reporting.

because healthcare is everywhere and always a cost benefit decision.

and you need free choice and sound data to make such choices well.

not exactly rocket surgery, is it?

or did you need another tour of the land of perverse incentives and regulatory capture?

October 23, 2022 Posted by | Corruption, Deception, Science and Pseudo-Science, Timeless or most popular | , | Leave a comment

Stanford tells doctors to give false information in order to overcome vaccine hesitancy

By Steve Kirsch | October 21, 2022

I found a Stanford course used to train doctors worldwide on how to overcome vaccine hesitancy. Basically, they tell doctors to give false information. They truly believe the false narrative.

Here’s the link for the Stanford course that teaches doctors how to overcome vaccine hesitancy.

It’s a series of short YouTube videos. It’s free to watch all the videos.

Here is the outline of the cases covered:

I viewed a number of the lessons to save you the pain and agony.

Some takeaways:

  1. They don’t expect to turn people around to support the vaccine in a single session. They admit it can take many sessions.
  2. They clearly think that people who don’t take the vaccine are simply misinformed and need to be set on the right track.
  3. They recommend giving people false information (like saying the risk of myocarditis is higher for the virus than the vaccine) in order to deal with their objections. Of course, they don’t admit in the course that their advice is false.
  4. At no time should the doctor try to learn anything from the patient (like that the doctor is wrong). It’s all about getting the patient to conform to the narrative, not to discover truth. None of the interventions are designed to examine the data or find the truth or allow the patient to change the doctor’s mind. You are never supposed to do anything like look at the data!
  5. I really think they should do their therapy session on me as one of their case studies. If they can show people how they set me on the “correct path,” that would be astonishing. It would be so entertaining to watch them try to do that. People would pay money to see that. I can’t figure out where I can volunteer to do that.
  6. One of the references is to a paper on why people resisted making the HPV vaccine mandatory. I can tell you why people resisted the HPV vaccine… that vaccine is the second most dangerous vaccine in VAERS, that’s why. Only the COVID vaccines are more dangerous. It has 3 times the number of adverse events that all other vaccines combined at the time it was introduced. That’s why!

Summary

If you want insight into how “they” think about “us,” this is a good reference.

October 23, 2022 Posted by | Deception, Science and Pseudo-Science | | Leave a comment

10 MINUTES COVID MADNESS. #NEVERFORGET

Credit: Professor Freedom

October 22, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | | Leave a comment

NEW EVIDENCE PROVES BIDEN ADMINISTRATION PRESSURED FACEBOOK AND TWITTER TO CENSOR AMERICANS

Liberty Justice Center | October 21, 2022 

Yesterday, author and data analyst Justin Hart filed new evidence in his federal lawsuit against Facebook, Twitter, and U.S. President Joe Biden. The evidence documents collusion between social media companies and the federal government to silence Americans online on the Internet — a public forum the Supreme Court has determined is the most important place for the exchange of ideas. Hart sued the social media giants and Biden administration in August 2021 for violating his First Amendment right to free speech for working together to monitor, flag, suspend, and delete social media posts it deems “misinformation.”

Hart is represented by attorneys from the Liberty Justice Center, a national public-interest law firm that fights to protect fundamental constitutional rights. Since filing the federal lawsuit, Liberty Justice Center, other nonprofit law firms, and state attorneys general have uncovered communications and documents proving collusion between Big Tech and Biden administration officials at every level. Hart’s attorneys have submitted this evidence gained through public records requests with an amended complaint.

“New evidence confirms what we have long known: our federal government is working directly with Big Tech to silence Americans,” said Daniel Suhr, managing attorney at the Liberty Justice Center. “The government is directing private companies to violate Americans’ free speech rights. Censorship may have started with what they call ‘COVID misinformation,’ but it opens the door for any administration to define any message they don’t like as ‘misinformation.’ This is unconscionable and illegal.”

Justin Hart is the author of Gone Viral: How COVID Drove the World Insane and founder of RationalGround.com. Over the last two years, his Facebook and Twitter accounts were suspended multiple times for sharing data and scientific research about COVID. At the time Hart’s statements and valid public health messages were censored, the facts were deemed “misinformation” by the Biden administration and Big Tech. However, much of what he shared about the detrimental effects of masking, lockdowns, and school closures are now widely accepted as true.

“The depth of the collusion between Big Government and Big Tech is alarming and reveals a sinister plot to undermine the rights of Americans by fully removing certain ideas and people from public discourse,” said Justin Hart, author and plaintiff. “The government does not have a monopoly on truth. By directing and pressuring social media companies to censor Americans, our government is silencing critical discussions and, most importantly, violating our most sacred rights.”

New evidence proves that prior to Justin Hart’s deplatforming in July 2021, the federal government and Big Tech coordinated regularly:

  • Facebook offered the federal government, and it accepted, $15 million in free COVID-19 public health advertising to promote its public health message on the Internet.
  • The Centers for Disease Control and Prevention (CDC) and Biden administration officials coordinated its COVID “misinformation” response with Facebook and Twitter by holding regular “be-on-the-lookout” meetings and by providing examples of the types of messages that contradicted the government’s message and it wanted censored.
  • Facebook used proprietary tools to monitor social media posts that contradicted the federal government’s COVID-19 narrative and reported such posts to the federal government.
  • Facebook adjusted its policies and algorithms to align with misinformation policies set by the federal government.

The lawsuit, Hart v. Facebook, was filed Aug. 31, 2021, and is being heard in the U.S. District Court for the Northern District of California, San Francisco Division. Case filings are available here.

October 21, 2022 Posted by | Civil Liberties, Science and Pseudo-Science | , , , | Leave a comment

We Will Be Challenging Any State’s Covid-19 Vaccine Requirement to Attend School

BY AARON SIRI – INJECTING FREEDOM – 10/20/2022

The CDC’s vaccine advisory committee unanimously voted a few hours ago to add the Covid-19 vaccine to the CDC’s routine childhood vaccination schedule. Immediately following the vote, I received a call from Del Bigtree, ICAN’s founder and host of The HighWire, to tell me that ICAN will support a legal challenge to any state that imposes a Covid-19 vaccine mandate to attend school.

We look forward to bringing those challenges to protect the individual right of every American, especially the youngest among us, as we successfully did when challenging the San Diego School District’s Covid-19 vaccine mandate. Everyone should be free to get numerous shots because that is freedom.  And everyone should be free to reject any unwanted shot because that, too, is freedom.

While most post-March 2020 mandates have been successfully challenged or rescinded, we must never forget that the repressive arm of government is just behind a curtain, waiting to strangle our rights. That is why we must fight, always fight, to push back against that oppression. It is not a war that is won. It is an endless battle with one side pushing the needle toward eliminating individual rights and the other side that must never stop pushing back – because once it swings too far, we will not easily regain our rights.  Power seized is rarely returned.

The next battle front is the body of every child in this country whose parents do not want them to receive a Covid-19 vaccine. A product for which you cannot sue the manufacturers for harm. A product whose clinical trial for children was underpowered, not properly controlled, and that did not review safety for a sufficient duration.  But even in the absence of these issues, corrosive rights-crushing mandates should never exist.

We look forward to, with ICAN’s support, challenging any state’s Covid-19 vaccine mandate for school.

P.S. Note that the CDC’s action of adding the Covid-19 vaccine to its routine childhood vaccine schedule does not automatically make it mandatory in all states for attending school. In most states, the state itself needs to take action to make it mandatory. The expectation is that some states will seek to do just that.

October 21, 2022 Posted by | Civil Liberties, Science and Pseudo-Science | , | Leave a comment

‘Gearing Up to Fight Biological Weapons?’ White House Launches $88 Billion National Biodefense Strategy

By Michael Nevradakis, Ph.D. | The Defender | October 20, 2022

The Biden administration on Tuesday announced a new $88 billion national biodefense strategy that outlines the government’s plans for how to respond to future pandemics, public health emergencies and biological threats.

The launch of the “National Biodefense Strategy and Implementation Plan for Countering Biological Threats, Enhancing Pandemic Preparedness, and Achieving Global Health Security” included the signing of National Security Memorandum-15 (NSM-15).

Key elements of the new strategy include the rapid production and distribution of vaccines and diagnostic tests, and enhancing global health security.

The strategy also includes a new framework for the federal government’s role during a future crisis, which places the White House at the center of any such response, coordinating the actions of multiple federal agencies.

The White House said the new strategy adopts lessons from the COVID-19 pandemic.

In an interview with The Defender, University of Illinois international law professor Francis Boyle, J.D., Ph.D., a bioweapons expert who drafted the Biological Weapons Anti-Terrorism Act of 1989, said:

“It appears that the enormous amount of money here, $88 billion over five years, when you add it on to well over, I would say, maybe $130 billion [in biodefense spending] since Sept. 11, 2001, means that they are gearing up to fight biological weapons warfare around the world.”

Boyle told The Defender that between October 2001 and October 2015, the federal government spent $100 billion “on biological warfare purposes.”

“To put that into perspective,” he said, “in constant dollars, the Manhattan Project to develop the atom bomb was $40 billion.”

Plan calls for development, distribution of new vaccines within 130 days

Biden’s new biodefense strategy includes the rapid development and deployment of new vaccines and diagnostics that it foresees in response to any future “biological threats.”

According to the White House’s plan, these “biological threats” may be “naturally occurring, accidental [or] deliberate,” “with the potential to significantly impact humans, animals (domestic and wildlife), plants, and the environment, and to negatively affect health, the economy, society, and security.”

According to STAT, the plan’s targets include:

  • Being able to test for new pathogens within 12 hours.
  • Making rapid tests available to the public within 90 days.
  • Repurposing existing drugs within 90 days.
  • Developing vaccines within 100 days.
  • Manufacturing enough of the new vaccine for the entire U.S. population within 130 days and “for the high-risk global population” within 200 days.
  • Developing new treatments within 180 days.

In justifying the new strategy, an unnamed senior Biden administration official quoted by The Hill said:

“We … know that the risk of another pandemic as bad or worse than COVID is a real threat. The new National Biodefense Strategy therefore outlines a bold vision … towards a world free of pandemics and catastrophic biological incidents.”

According to Defense One, other goals contained within the plan include “detecting the spread of pathogens before patients even begin to show symptoms like fever” and “scaling up the number of diagnostic test kits by tens of thousands within a week.”

A further element of the plan is “restoring community, the economy and the environment after a pandemic or biological incident,” The Hill reported.

The Biden administration’s plan also includes provisions for preparedness against the “accidental release of biological agents, and threats posed by terrorist groups or adversaries seeking to use biological weapons.”

Noting that COVID-19 “has highlighted that the United States and the world are vulnerable to biological threats, whether naturally occurring, accidental, or deliberate,” the plan states:

“It is a vital interest of the United States to prepare for, prevent, detect, respond to, and recover from biological threats at home and abroad.

“Therefore, countering biological threats, advancing pandemic preparedness, and achieving global health security are top national and international security priorities for the United States.

“Moving forward, the United States must fundamentally transform its capabilities to protect our Nation from biological threats and advance pandemic preparedness and health security more broadly for the world.”

According to STAT, an unnamed senior Biden administration official said Tuesday, “One of the important things that COVID has taught us is that we need to be able to move much faster to counter pandemic threats, and we also need to be prepared for completely unknown threats.”

The same official said the plan includes “moonshot” targets that are not scientifically feasible presently, but potentially could be within a decade.

According to the official, these new developments can target the 26 families of viruses that infect humans, “many of which we are far less prepared for than coronaviruses.”

Will Congress fund it?

Some questioned the plan’s price tag and the willingness of Congress to approve its funding.

One of the elements of the new strategy is its connection to a March 2022 request to Congress for $88 billion in funding over five years for “pandemic preparedness and biodefense,” a request that has thus far “stalled.”

These monies are intended, in part, “to fund new research to predict outbreaks before they become pandemics,” and “accelerate rapid testing to get ahead of where viruses are moving,” Defense One said.

Some of this money will come from the baseline funding of the federal agencies involved in this strategy, but it’s unclear whether Congress has “much of an appetite for additional public health spending,” according to STAT, which noted that “Republicans in Congress have balked at recent requests for funding the ongoing monkeypox and COVID-19 responses.”

According to the White House, the new strategy “builds on USAID’s [U.S. Agency for International Development] announcement earlier this year committing $150 million to the Coalition for Epidemic Preparedness Innovations to accelerate the development of life-saving vaccines and countermeasures against biological threats.”

The White House also included the $1.4 billion in “seed funding” it provided earlier this year to the “groundbreaking new Financial Intermediary Fund for Pandemic Prevention, Preparedness and Response at the World Bank.”

Boyle described the $88 billion in projected funding over the next five years as “a dramatic escalation” with “no justification from legitimate scientific reasons.”

He noted that since 2015, the federal government has “allocated anywhere from $5 to $6 billion per year on biological warfare purposes, which, being conservative, would mean a sum total from Sept. 11, 2001, until now, of $135-$140 billion.”

In his view, this money is being allocated “into further expanding the U.S. biological warfare industry … for the purpose of waging biological warfare,” and instead “should have been spent on the public health of the American people.”

‘You find Tony Fauci behind all of it’

Part of the price tag for the new biodefense strategy appears to be directed toward “recruiting, training and sustaining a robust, permanent cadre of health workers in all 50 states,” in the words of a senior Biden administration official quoted by Reuters.

Referring to it as a “public health army,” STAT reported that this “cadre of health workers” will include “laboratory technicians, veterinarians, and community health workers — to not only better detect emerging diseases but respond to them.”

In turn, Defense One reported that the strategy “aims to boost the number of local healthcare workers” and “traditional frontline healthcare workers,” but also, many new positions “related to research and data collection,” including “expanding the CDC’s epidemiology field officer program” and “bringing more epidemiologists to every state.”

The Biden administration also said it is “committed to helping at least 50 countries strengthen their own local capacities,” “strengthening public health workforces both in the United States and globally” and “establishing international mechanisms to bolster laboratory safety,” according to STAT.

For some, “international mechanisms” may bring to mind the recent and ongoing efforts by the World Health Organization (WHO) to establish a renewed “global pandemic treaty” — efforts in which the United States under the Biden administration has played a leading role.

As previously reported by The Defender, the Biden administration expressed broad support for a “pandemic treaty” and previously headed negotiations on this issue.

In his interview with The Defender, Boyle also drew connections between the Biden administration’s new strategy, and efforts to develop the “pandemic treaty.”

Referring to the Biden administration’s recently signed executive order on “advancing biotechnology and biomanufacturing,” Boyle remarked that it makes mention of “dual-use research of concern, and research involving potentially pandemic and other high-consequence pathogens.”

For Boyle, “dual-use research” refers to the development of both “offensive and defensive biological weapons of warfare,” noting that “when it comes to biological warfare, defense means offense.”

“If they are saying they are doing all this for defensive purposes, it’s because they are also planning offensive use of biological warfare weapons, with the defense to defend themselves in the event that adversaries respond in kind,” Boyle added.

This then connects to the “pandemic treaty,” according to Boyle, noting that Dr. Anthony Fauci has close ties to the WHO’s executive committee:

“If you recall, Trump pulled us out of the WHO. The first act Biden did was to put us back into the WHO … and he appointed Tony Fauci as the U.S. government’s representative on the WHO executive committee.

“So the same guy supporting this ‘dual research of concern’ … is also implementing, supervising this new WHO treaty.”

Biden’s strategy also “calls for international mechanisms that can help strengthen lab safety and biosecurity practices around the world,” especially in light of “questions about the risks and benefits of research into potentially dangerous viruses,” including the COVID-19 Wuhan lab-leak theory.

This may indicate that Biden is seeking to expand gain-of-function research globally. As recently reported by The Defender, facilities conducting such research — including a facility where a purportedly “more lethal” strain of the COVID-19 Omicron variant was developed — are currently being expanded in the U.S.

Gain of function refers to the “manipulation of pathogens to make them more dangerous,” in the hope of “getting ahead of a future outbreak.”

As part of the new strategy, a “policy coordination structure for biodefense among government agencies with oversight by the White House” was signed, Reuters reported.

According to The Hill, this memorandum “outlines the coordination structure for biodefense across federal agencies, directs agencies to prioritize biodefense, directs the intelligence community to track evolving threat landscapes and ensures the government is continuously reviewing and adjusting priorities.”

Boyle, an outspoken critic of gain-of-function research, said it appears such research will be an integral part of the Biden administration’s new biodefense strategy. He told The Defender :

“It’s clear in the language that they are going full steam ahead on abusing DNA, genetic engineering, gain-of-function, synthetic biology, gene splicingCRISPR-Cas9, to develop biological warfare weapons.”

He said that the proposed WHO pandemic treaty includes language on “measures to provide oversight and report on laboratories that do work to genetically alter organisms in order to increase pathogenicity and transmissibility.”

For Boyle, “this means gain-of-function work, using and abusing DNA engineering, synthetic biology, CRISPR-Cas9. That’s in the WHO treaty.”

“It all ties up,” Boyle added. “The executive order, the biodefense strategy, the WHO treaty. You find Tony Fauci behind all of it.”

Boyle added:

“When you add all this up together, it seems to me they’re gearing up to prepare to wage offensive biological warfare and preparing for the defense, for other states to respond with biological warfare weapons.”

Plan calls for coordination across federal agencies under White House control

The administration’s new biodefense strategy will utilize more than 20 federal agencies, while “oversight for the strategy will be at the White House, under the national security advisor.”

According to a  senior Biden administration official, the new strategy “directs the U.S. intelligence community to monitor for threats and ensure the United States ‘continuously adapts to this evolving threat landscape’ by holding annual exercises,” to “prevent epidemics and biological incidents before they happen,” Reuters reported.

This may bring to mind exercises and simulations that took place just prior to the COVID-19, monkeypox and anthrax outbreaks, which appeared to predict, with remarkable similarity, what was to follow.

According to Biden’s new strategy, the heads of the relevant federal agencies “shall implement the Biodefense Strategy, as well as related strategies such as the U.S. Global Health Security Strategy, and include biodefense-related activities … within their strategic planning and budgetary processes.”

Federal agencies also will be expected to coordinate with each other and with non-federal agencies on matters pertaining to “the biodefense enterprise.”

Is new strategy a ‘moonshot,’ or ‘pie-in-the-sky’?

In addition to questions about funding, some also questioned the feasibility of the new plan.

Defense One wrote that meeting some of the “moonshot” goals of the strategy “will require scaling up data-collection efforts at research facilities around the globe,” in addition to significantly ratcheting up a host of other research-related efforts, noting that the administration “did not specify exactly what technologies they will invest in.”

According to Defense One, “new approaches to RNA research” to “ease pandemics” may need to be developed, in addition to “new forms of plant-based vaccines” that could “allow for the scaling up of vaccine production by orders of magnitude.”

An unnamed senior Biden administration official quoted by Defense One acknowledged that the “moonshots” foreseen by the plan “are not possible today, but these capabilities can be achieved and are within our reach with the right resources over the next five to 10 years.”

Hiring more health workers may also prove challenging for the Biden administration due to a shortage of nurse practitioners that is expected to grow by 2025, along with looming “shortages of other healthcare workers.”


Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV’s “Good Morning CHD.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

October 21, 2022 Posted by | Deception, Militarism, Science and Pseudo-Science | , | Leave a comment

Aortic Dissection after COVID-19 Vaccination

Some Injuries are for Keeps

By Dr. Peter McCullough & John Leake | Courageous Discourse | October 21, 2022

Yesterday I met a 42-year-old optometrist who six days after the second mRNA COVID-19 vaccination suffered a distal aortic dissection. He was healthy and was physically fit. He knew something was wrong when back pain and leg weakness developed resulting in severe effort intolerance on vacation. He rushed home, was hospitalized and underwent the appropriate diagnostics to determine the presence of an aortic aneurysm or widening of the aorta and then a discrete tear which blood flow now goes through the true lumen and a false lumen created by the dissection. This occurs in the outer third of the media or the muscular layer of the blood tube.

In his mind this catastrophic event is due to the COVID-19 vaccine, and I agree. The mRNA and Spike protein produced by the mRNA circulates in blood on average two weeks, so it is freely able to deposit in the lining of blood vessels and the vascular media of major vessels.[i] [ii] Once present, the Spike protein damages cells and incites inflammation which is a destructive process driven by white blood cells, cytokines, and complement. It is known that the second injection is approximately 80-fold more reactogenic with fever, pain, myalgia, etc. As part of that response, there can be a major surge in blood pressure due to release of catecholamines or stress hormones.[iii] This increase in the change in pressure over the change in time for each heartbeat is the driving force to initiate the tear in the aorta. Once this happens, there is no turning back, the rip goes down the major blood tube and threatens the blood supply to the spinal cord, vital organs, and legs. Each patient is different, with some having external rupture resulting in death. Others require emergency surgery or endovascular stenting to restore blood flow to vital organs. In the case of the optometrist, he was managed conservatively with medications to control blood pressure. Data from the International Registry of Acute Aortic Dissection (IRAD) indicates he faces a 22% 3-year mortality rate and this is increased by his history of prior aortic aneurysm (HR, 2.17; 95% CI, 1.03 to 4.59; P=0.04).[iv] It is exactly this complication for which I have always advised patients with prior aortic abnormalities (aortopathies) to avoid COVID-19 vaccination.  If you know someone who has died shortly after vaccination and they had antecedent back pain or a prior aneurysm, ask the family if there was an autopsy. This is important since aortopathies can be familial and other family members could be screened with imaging and genetic testing. This man’s life is indelibly changed because COVID-19 vaccination was for “keeps.”

October 21, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular | | Leave a comment

The crushing of dissent throughout the covid era

Orwellian parallels worsen by the week

Health Advisory & Recovery Team | October 8, 2022

The recent actions of the financial technology company, PayPal, to close the accounts of subscribers expressing political opinions of which they disapprove, represents the latest example of censorship within so-called liberal democracies. Their strategic decisions to block the online monetary activities of the Free Speech Union, the Daily Sceptic website and the Us For Them campaign group – although later reversed – signal the willingness of powerful global big-tech companies to collude with governments in the crushing of activities that challenge the dominant narratives.  But no one should be surprised; we have all been manipulated by top-down censorship and state propaganda for many years, a dystopian process that accelerated during the covid era.

Since the emergence of the novel coronavirus in early 2020, there has been widespread censorship of views that do not support the two mantras of covid-19 orthodoxy: namely that, ‘Lockdowns and other restrictions were appropriate responses’ and ‘The mRNA vaccines are safe and effective’. Indeed, the unprecedented and non-evidenced covid restrictions could not have been so successfully imposed without propaganda in all its forms. Contrary to popular opinion, techniques of manipulation do not only characterise recognised totalitarian regimes, but are now endemic within contemporary liberal democracies. And three, overlapping, forms of non-consensual persuasion have been widely deployed throughout the covid era to control the narrative and subsequent behaviour of citizens:

1.      Control through emotional manipulation

The covert influencing of people’s emotions via use of behavioural-science ‘nudges’ has been well documented. Based on the advice of state-employed psychological experts, the covid-19 communication strategy has relied heavily on evoking uncomfortable feelings in the populace as a way of inducing them to ‘do the right thing’, where what is ‘right’ is solely determined by government-appointed officials. In particular, the manipulation of fear, shame and scapegoating – or ‘affect’, ‘ego’ and ‘norms’, to use the euphemisms of behavioural science – has been conducted for this purpose via the broadcasting of selective statistics, alarming images and emotional messaging. Furthermore, the decision to impose mask mandates was most likely informed by the knowledge that face coverings enhance the power of each of these three nudges, thereby increasing people’s compliance with government diktats.

Despite escalating concerns about the ethical basis of the state’s deployment of behavioural science, there has been a stark reluctance of anyone in authority to accept responsibility for this form of manipulation. The British Psychological Society (the formal guardians of ethical application of psychological interventions) is of the view that covertly inflicting emotional distress on people so as to promote compliance with covid restrictions and the vaccine rollout is acceptable as it is encouraging ‘social responsibility’, thereby colluding – along with other professional bodies – with the state’s mission to silence dissent and eliminate contrary behaviour. Meanwhile the Government show a reluctance to explore the ethics underpinning their deployment of nudges as evidenced by their ‘Public Administration and Public Affairs Committee’ ignoring a request for an independent inquiry and the omission of any mention of behavioural science in the draft terms of reference for the Inquiry into the covid-19 pandemic.

2.      Control through modulating the flow of information

A second way of controlling dissent – used at unprecedentedly high levels throughout the covid event – has been via the regulation of information flow within our TV, radio, newspaper and social media outlets. Ease of access to facts, data and opinion (including that of scientific experts) has been mainly determined by the degree to which the information corresponds with the dominant narratives: write or speak words supportive of lockdowns, masking and vaccination and they will typically receive preferential treatment within the media’s editorial processes, gaining prominence and ease of access; in contrast, say or print something contrarian and it will most likely be submerged in the quagmire of daily media output.

The seeds of this system of selective information flow had been sown prior to 2020 with the formation of the ‘Trusted News Initiative’ (a coalition of mainstream media, publishers and big-tech companies) aspiring to ‘create a global alliance of integrity in news’ by countering ‘misinformation’ and ‘bias’. Furthermore, at the start of the pandemic, Ofcom – the UK’s communications regulator – instructed broadcasters not to cover anything that went against the Government’s narrative. This censorial alliance ensured that voices expressing dissent about covid restrictions and the vaccine rollout were disadvantaged, displaced to the inaccessible fringes of media output.

In the UK, there has even been military involvement in the form of the 77th Brigade with their explicit mission to create and spread material ‘in support of designated tasks’ while also ‘supporting counter-adversarial information activity’. Internationally, the WHO has effectively modulated the flow of information via the use of fact-checking organisations and collaborations with Facebook, Twitter, WhatsApp and YouTube, so as to guarantee that ‘science-based health messages from official sources’ (aka the dominant narrative) appear first when one searches for covid information.

Specific examples of the impact of this – seemingly global – operation to control information flow are numerous. They include: Professor Gupta (an epidemiological expert) being instructed not to mention the Great Barrington Declaration prior to appearing on a BBC discussion programme about lockdowns; academic journals blocking the peer-reviewed covid research of Dr Peter McCullough and the suppression of trial findings that had concluded that Ivermectin was an effective treatment; the removal of Dr Robert Malone (the inventor of mRNA technology) from Twitter; and the removal of MPs Sir Christopher Chope and David Davies from YouTube for, respectively, raising concerns about vaccine damage and vaccine effectiveness.

One fundamental consequence of this selective regulation of information was that our Western media – a supposed pillar of democracy – failed us all in their refusal to scrutinise and evaluate the actions of public officials.

3.      Control through erasing dissenting voices

Presumably based on the assumption that eliminating people before dissent is expressed is a more effective censorial method than controlling their information output, throughout the covid era there appears to have been a systematic state-driven attempt to discredit or cancel those brave individuals expressing views that are inconsistent with the dominant restrict-and-jab narrative.

Since March 2020, anyone who has expressed a contrarian covid opinion in a public space will likely have attracted criticism involving accusations of being ‘right wing’, fascist or a ‘conspiracy theorist’. Efforts by powerful players to destroy reputations and livelihoods through smearing and character assassination have been commonplace. Arguably the most high-profile example of this egregious practice is in regards to the targeting of the main authors of the Great Barrington Declaration, a multi-signatory document arguing for an alternative to the blanket lockdowns. In leaked emails between Anthony Fauci (Chief Medical Advisor to the US president) and Francis Collins (the Director of the US National Institute of Health), these powerful state officials refer to the illustrious authors of the document as ‘fringe epidemiologists’ while describing the need for a ‘quick and devastating public takedown’ of their arguments. Furthermore, the extremely popular US podcaster, Joe Rogan, was smeared as a transphobe and racist in the aftermath of him giving a platform to experts expressing views at odds with the dominant covid narrative.

A threat of imminent loss of earnings – actual or implied – is another tactic that has been commonly deployed to cancel those criticising the approach of Western governments to pandemic management. Many academics have suffered in this way, including Canadian professor Julie Ponesse who lost her job after she challenged the vaccine mandates. Of course, such a draconian sanction serves as a warning to many other university scholars who might also be considering expressing dissent.

The recent actions of PayPal suggest that our medico-technocratic powerhouses are not satisfied with inflicting emotional distress, censorship and character assassination on the Western population, but now seek to control how we spend our money. Manipulation by means of regulating access to our finances may be the new front in the war on freedom of verbal and behavioural expression. It raises the spectre of the imposition of a totalitarian social credit system, mediated via a Central Bank Digital Currency, a world where unelected global bureaucrats determine our monthly spend based on the degree to which our behaviour conforms to their version of what constitutes the ‘greater good’.  

In the words of Piers Robinson (an expert on global propaganda), ‘That the censorship, smearing and coercion … has come to be tolerated is a clear indicator of how far our democracies have slipped into an authoritarian abyss’. And the imminent Online Harms Bill, with its ‘legal but harmful’ category, may further restrict our basic human right to freedom of expression. But there is still hope. As more and more people become aware of the associated collateral damage, the dominant narratives on the benefits of lockdowns, school closures, masks and ‘safe-and-effective’ covid vaccines are beginning to crumble. As awareness of ubiquitous state-funded manipulation and censorship grows, increasing numbers of citizens are turning to independent sources of expert information – such as HART and PANDA – for reliable covid updates. The basic human right of freedom of expression within Western democracies must be protected; once lost, it is unlikely to be restored within our lifetimes.

October 21, 2022 Posted by | Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science | , , , | Leave a comment

No balanced coverage of covid vaccines in legacy media, says Peter Doshi

By Maryanne Demasi, PhD | October 16, 2022

Peter Doshi, associate professor at the University of Maryland School of Pharmacy and senior editor at The BMJ, has spoken out about how the mainstream media has ignored important data on covid-19 vaccines.

In a recent interview with German TV, Doshi said, “Our legacy media has not done a good job in providing balanced coverage about the vaccines.”

He said there has been “a lot of nervousness” about how to communicate vaccine harms to people and is concerned that “we’re not getting the information we need to make better choices and to have a more informed understanding of risk and benefit.”

Doshi’s concerns extended to the over-confidence of public health authorities engaged in promoting the covid-19 vaccines.

“It was very unfortunate, that from the beginning, what was presented to us by public health officials was a picture of great certainty… but the reality was that there were extremely important unknowns,” said Doshi who has written and spoken about these unknowns, highlighting that even public health officials were aware of these limitations.

“We entered a situation where essentially the stakes became too high to later present that uncertainty to people.” He added, “I think that’s what set us off on the wrong foot. Public officials should have been a lot more forthright about the gaps in our knowledge.”

A pivotal study

Doshi was part of an international group of eminent academic researchers and physicians who went back and re-analysed the safety data from the original randomised clinical trials that underpinned the FDA’s decision to authorise the mRNA vaccines in December 2020.

reported on the pre-print study, but since then, it has been published in the peer-reviewed journalVaccine.

The authors focused on serious adverse events that occurred in the Moderna and Pfizer vaccine trials, events the sponsors classified as “serious” generally because they resulted in hospitalisation.

In short, their analysis showed that mRNA vaccines were associated with 1 additional serious adverse event for every 800 people vaccinated, which Doshi said is “much more common” than what we’ve traditionally observed for other vaccines where the adverse event rate is in the range of 1 to 2 per million vaccinees.

“Just to put that in some perspective, a rate like that in past years has had vaccines taken off the market. In 1976, we saw Guillain Barre Syndrome after influenza vaccines that were then withdrawn.”

The authors of the study also found the trial data showed that the increase in serious adverse events following mRNA vaccination surpassed the reduction in risk of ending up hospitalised with covid-19.

Preventing transmission

Despite public assurances that covid-19 vaccines would save lives and protect the community by preventing transmission, Doshi knew from the outset that it was never properly tested. In Oct 2020, Doshi published an article in The BMJ:

Hospital admissions and deaths from covid-19 are simply too uncommon in the population being studied for an effective vaccine to demonstrate statistically significant differences in a trial of 30 000 people. The same is true of its ability to save lives or prevent transmission: the trials are not designed to find out [emphasis added]

It was, therefore, unsurprising to Doshi that the vaccines failed to stop the spread.

“One of the big reasons is that it’s an intramuscular vaccine, and this doesn’t produce mucosal immunity.  Infections of covid, influenza and other acute respiratory infections, start in the mucosal membranes, a place where these vaccines are not particularly good, historically, at producing immunity antibodies” said Doshi.

Calling for raw data

Doshi and his colleagues have called on public health authorities and drug manufacturers to release the raw data so that we can better understand who is most at risk of a serious adverse event.

“There’s no reason to think that these risks are going away and if it’s in the low-risk population, that’s very bad news, because low-risk people have much less to potentially gain from covid vaccines, so the side effect profile in such people has to be extremely low,” said Doshi, pointing out that Denmark now recommends against routine covid-19 vaccination for people under 50.

The FDA and the vaccine manufacturers have the raw ‘patient level’ data, but they have not released it and we’re now almost 2 years into the roll out of the product.

“They should immediately be warning people about this safety signal that we found, and they should immediately be replicating our analysis — the data are indicating there’s increased risk at a level that is much higher than has previously been realised,” said Doshi.

Throughout the pandemic, we’ve been told to “trust the science” but Doshi says, “How can one recommend responsibly that these products are based on science if the data are not available?  Science is about sharing data. We’re in an era of open science, not secret science.”

Doshi and colleagues have penned an open letter to the CEOs of the vaccine companies asking for the raw data, but as yet, they have not received a reply.

See the full interview on mdr.de

October 21, 2022 Posted by | Deception, Mainstream Media, Warmongering, Science and Pseudo-Science | , | Leave a comment

ACIP committee approves mRNA vaccines for the childhood schedule 15-0

By Steve Kirsch | October 20, 2022

The ACIP committee voted on Thursday, as predicted, to add the COVID vaccines to the childhood vaccination schedule so that the manufacturers will now get full liability protection for the authorized product forever.

Here’s the Reuters story that was just published:

U.S. CDC advisers approve adding COVID shots to vaccine schedules

The last of the public commenters was cut off because they were talking about Nuremberg. They were asking why do you even have a public comment section because nobody listens to the comments.

The ACIP committee voted 15-0 to approve the mRNA COVID shots for the childhood immunization schedule, just as I and others predicted they would.

See Meryl Nass’s writeup on her prediction which just came true a few minutes ago.

This means several things:

  1. The “emergency” can now end. They needed the emergency to be able to create EUA approval which gave them liability protection as long as the emergency existed. The emergency is no longer needed.
  2. The vaccine makers can now manufacture fully “approved” vaccines and have complete liability protection forever.
  3. The ACIP vote is just a recommendation. The CDC must add it to the schedule, but that’s a slam dunk.

How corrupt are these people? Very corrupt.

These people do not want to see any data that shows the vaccines are not safe.

I tried to ask the Chair of the ACIP committee, Grace Lee, if she wanted to see the Israeli safety data showing the vaccines aren’t safe. She refused to answer my Yes or No question on this important data and called the cops on me (even though I didn’t violate any laws). I have it all on video.

That is the level of corruption we are dealing with here: “scientists” who simply look the other way when asked if they want to see the safety data.

My video erases all doubt that they could be honest. The cop handed her my note so I know she got it. She never responded to the offer. They don’t want to look at any negative data.

This means COVID shots will be required in certain states

The Reuters article contained this statement:

“Adding the COVID-19 vaccine to the recommended childhood immunization schedule does not constitute a requirement that any child receive the vaccine,” said Dr. Nirav Shah, an ACIP member and Director of Maine’s Center for Disease Control and Prevention.

What Dr. Shah failed to point out is that there are many states which adopt the entire childhood schedule as a requirement to attend public school. So sure, the vote doesn’t force anyone to follow it, but the reality is that it will be mandated in those states that require the entire vaccine schedule. That point was conveniently left out.

See it happen

Meryl Nass live commentary

Summary

We all knew this was going to happen. I still don’t know of a single healthy kid who died from COVID. We do know of healthy kids who die from the shot. This is insanity and few members of Congress have the guts to speak out about this.

If you haven’t supported Senator Ron Johnson in the past, this would be a very good time to donate to his campaign. It is imperative he win. Please read this article and make a donation using the link in the article. Thanks!

October 20, 2022 Posted by | Corruption, Science and Pseudo-Science, War Crimes | , | Leave a comment

Where Are All the Vaccine Safety Reports the MHRA Promised Us, Ask Doctors and Scientists

BY WILL JONES | THE DAILY SCEPTIC | OCTOBER 19, 2022

The Health Advisory and Recovery Team (HART), an expert group of medics, clinicians, scientists and academics, has published an article reminding the U.K. drug regulator, the MHRA, that it initially set out a solid plan of how it would monitor the safety of the Covid vaccines it had approved for emergency use. It asks what happened to that plan and all the vaccine safety reports promised under it.

The article starts by setting out the ways in which the MHRA has fallen short in its duty to regulate the vaccines.

The U.K. drug regulator, the MHRA, did not carry out the toxicity, biodistribution and pharmacokinetics studies that are required of new drugs because of the political pressure to approve. However, nearly two years have passed since then and the MHRA has not set a deadline for the pharmaceutical companies to provide these data. The MHRA allowed the treatments to be presented as vaccines like any other when they are a novel class of agents, never before approved for human use despite the technology being around for decades (mostly because they have been dangerous and ineffective in previous human trials).

The trials should have remained placebo controlled and ongoing for two to five years minimum in order to establish an understanding of their safety. Authorisations were based on two months of safety data in healthy people and the MHRA allowed the pharmaceutical companies to vaccinate the placebo control group such that further safety data could not be collected.

Approvals for children were unethical when the trial data did not show evidence of a benefit from the drug to the children themselves when there was already good evidence of short term safety issues and when long term safety data was inevitably unavailable. Approving for younger children after the arrival of Omicron was even less defensible.

The MHRA failed to notice that the total mortality in the trial was higher in the vaccination group than the placebo group, showing no evidence of an overall mortality benefit, and the serious adverse reactions were much higher in the vaccination group such that one in 800 participants were hospitalised for a non-Covid condition, which far outweighed the small reduction in Covid hospitalisations.

Dame June Raine, the head of the U.K. drug regulator the MHRA, appeared to take a unilateral decision to change its role. She said “the Covid pandemic has catalysed the transformation of the regulator from a watchdog to an enabler.”

The regulator receives 86% of its funding from industry fees. In 2005, the House of Commons’ health committee expressed concerns regarding the U.K. drug regulator that pharmaceutical funding could lead the agency to “lose sight of the need to protect and promote public health above all else as it seeks to win fee income from the companies”. Do we want a regulator which sees itself as an enabler of pharmaceutical companies?

At the outset, the MHRA set out an excellent plan for safety monitoring of the Covid vaccines which was required because of the minimal safety data from trials and the planned extensive rollout. It described this as a four part system of “proactive vigilance… to rapidly detect, confirm, characterise and quantify any new risks that were not detected in clinical trials”.

The four parts were:

1. Have doctors report concerns to the Yellow Card system
2. Actively analyse GP data on a weekly basis to look for increases in any suspected condition
3. Proactively survey to follow up a sample of people after vaccination
4. Academic studies of large medical databases

The only publications from the MHRA in the last two years on safety have been the Yellow Card reports and even these do not divulge the number of people affected or the seriousness of the reports.

Where are these weekly analyses of GP data, proactive surveys of the vaccinated and academic studies of large medical databases? We’re approaching two years into the rollout – where are all these promised reports? And why is no one apart from HART and a smattering of others asking these questions?

Worth reading in full.

October 20, 2022 Posted by | Corruption, Deception, Science and Pseudo-Science, Timeless or most popular | , | Leave a comment

Spike Protein Triggers Coronary Plaque Destabilization and Thrombosis

By Dr. Peter McCullough & John Leake | Courageous Discourse | October 20, 2022

As a cardiologist, I have received many reports of cardiovascular events (unstable angina, myocardial infarction) occurring after COVID-19 vaccination. Each vignette is different from an explosive fatal heart attack to rapid progression of coronary disease and the need for stenting or bypass surgery. A study by Gundy, who measured multiple biomarkers before and after vaccination was presented as an abstract at the American Heart Association; it predicted heart attacks would happen with COVID-19 vaccination based upon indicators that atherosclerotic plaque within coronary arteries would destabilize with circulatory Spike protein and cytokines.[i] This inflammatory milieu in combination with the thrombogenic nature of the Spike protein is a recipe for fatal and nonfatal heart attacks in patients with existing coronary disease.

This is different from myocarditis which is direct heart inflammation that can occur in younger people with normal coronary arteries. To the casual observer if a man over age 50 years drops dead a few weeks or a few months after a COVID-19 vaccine, it is possible the mechanism of death may have been a fatal myocardial infarction and thrombotic blockage of a coronary artery to heart muscle as depicted in the figure. The only way to tell if the cause of death was coronary heart disease or myocarditis would be to obtain a limited autopsy. Baronti et al reported on four fatal myocardial infarction cases occurring shortly after COVID-19 vaccination.[ii] All of the patients underwent autopsies and were found to have predisposing factors to blood clots. Patients with prior heart attacks, stents, and bypass surgery are at unacceptably high risk for progression of disease after COVID-19 vaccination and despite the fearful fervor of their cardiologists, they should respectfully decline the shots to keep their cardiovascular system safe. COVID-19 is always treatable and so many heart patients have already had the illness so the next episode will be characteristically mild. Because SARS-CoV-2 respiratory illness can trigger cardiovascular events in the months after hospitalization, recovering patients should consider themselves at equal risk to those who have taken the vaccine and report new heart symptoms to their cardiologist.[iii] Probably the highest risk patients are those who have had severe COVID-19 and have taken multiple injections either before or after the respiratory infection. In these cases, multiply loading the body with long-lasting Spike protein is highly likely to be an ongoing danger to the cardiovascular system and the only way to navigate out of the storm is to decline any further injections and let the body slowly recover.

October 20, 2022 Posted by | Science and Pseudo-Science | | Leave a comment