Prion Disease and the mRNA Shots: Some Light in the Dark
By John-Michael Dumais | The Defender | July 6, 2023
In a 2022 paper, Stephanie Seneff, Ph.D., Peter McCullough, M.D., MPH, and others discussed how the COVID-19 mRNA vaccines produce G-quadruplexes and microRNAs that can lead to prion disease.
The effect becomes significantly worse after the second dose of the Pfizer shot.
Prions are pathogenic agents that can induce the abnormal folding of cellular proteins, leading to diseases such as bovine spongiform encephalopathy (mad cow disease), Creutzfeldt-Jakob disease (CJD) and Alzheimer’s.
In his June 20 Substack post, researcher Adam Gaertner provides an accessible mini-tutorial on the complex and inspirational nature of cellular proteins. He addresses the structure and function of prions, the mechanisms by which they form, and how they can wreak havoc on any organ, especially the brain.
Prion disease can lead to a number of rare, progressive neurodegenerative disorders such as dementia, ataxia and spasticity before it becomes fatal, typically within just a few years of diagnosis.
Gaertner challenges the orthodoxy that there is no cure for prion disease by discussing several recent discoveries that offer “some unexpectedly good news.”
Innate immune suppression by SARS-COV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes and micrornas. Credit: Seneff, Nigh, Kyriakopoulos and McCullough.
Further investigation into mRNA and CJD
Gaertner began his research work into potentially useful therapeutics for prion disease and has also funded the development of a non-invasive prion blood test.
He even undertook his own study of people who were diagnosed with or died of CJD-like symptoms (n=60) after receiving the (mostly Pfizer) mRNA jab.
Nevertheless, he readily admits that he has yet to establish absolute proof of causation.
In a European Union document related to the approval of the vaccine, Gaertner discovered what could be the smoking gun: The liquid nanoparticles used to encase the mRNA came primarily from cow fat. According to Gaertner, the document in question even admitted mRNA’s potential to cause prion protein contamination.
Nearly a year after Gaertner publicized his discovery — which convinced some but not all researchers — a paper by Jean-Claude Perez documented 26 cases of “a new form of CJD” observed within a few days of the Pfizer, Moderna or AstraZeneca vaccinations.
Of these, 20 people died within less than five months of the injection. (At the time of the paper’s publication, only one of the 26 had survived.)
The ‘good news’
While admitting that “there is not, ordinarily, a whole lot of good news to be had concerning prion diseases,” Gaertner outlined a mechanism by which “residues on the spike [protein] bind to the many and varied amyloidogenic proteins,” thus resulting in the blood clots observed by more than a few embalmers since the introduction of the mRNA shots.
He explained how this process can “bind up” the prionic proteins:
“So, what we essentially have here is, instead of a silently cascading apocalypse, buried deep inside parts of the brain that we will never reach, we likely, instead, have these long, stringy, vein-shaped agglomerations of the various amyloid proteins, binding together wherever they meet, and apparently at least somewhat resistant to being broken down by the body’s natural processes for dealing with such eventualities.”
The “really good news” comes from the way ivermectin binds directly to the spike protein — which has itself been described as a “prion-like” protein — thus blocking the spike from connecting to the ACE-2 receptor and “preventing the key from ever entering the keyhole.”
According to Gaertner, ivermectin also prevents the “amyloidogenic aggregations to the spike protein,” thereby arresting the production and proliferation of the prionic proteins. He adds:
“Ivermectin is, without a shadow of a doubt at this point, a true miracle drug: With so many applications, from antiviral, to cancer treatment, to anti-inflammatory, and of course in its originally recognized anti-parasitic application, there should be little wonder why the powers that be have done their best to diminish it as ‘horse paste.’”
Gaertner also notes that in a “very unscientific poll” he conducted on Twitter, 80% of respondents reported that a single, low dose of ivermectin significantly improved “brain fog,” a common post-COVID-19 symptom.
He described a number of “relevant investigational therapeutics” for use against the spike protein and its effects, including serrapeptase, quercetin, methylene blue and resveratrol, some of which demonstrate a “very broad range of useful actions.”
Expressing his belief that the lack of progress on therapeutics for neurodegenerative diseases is likely due to “your run-of-the-mill Pharma and charity corruption,” Gaertner nonetheless found cause for optimism.
“There’s been a lot of progress, on a lot of fronts, and more comes regularly as the world continues waking up,” he said.
John-Michael Dumais is a news editor for The Defender. He has been a writer and community organizer on a variety of issues, including the death penalty, war, health freedom and all things related to the COVID-19 pandemic.
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.
Now that government COVID malfeasance is exposed, what will the GOP do about it?
By Daniel Horowitz – conservative review – July 6, 2023
We are now 2+ years into consuming reams of information showing the vaccines were devastating to humanity. What will Republicans do about it other than whine about censorship? Refusing to focus on vaccine injury and the perfidy of the government-vaccine complex is an act of self-censorship.
There is a bizarre dynamic unfolding as it relates to GOP sentiment toward the vaccine. All Republicans recognize and decry the growing evidence of the government’s collaboration with big tech to censor all information about vaccine injury. Yet they seem to be more upset about the censorship of the information than about the information itself. Why is there no push from Republicans to defund the vaccines and fix the regulatory and legal structures that allowed Operation Warp Speed to occur and that continue to gaslight the next iteration of rushed, dangerous vaccines?
In an extraordinary ruling on Independence Day itself, Louisiana federal Judge Terry Doughty issued a broad injunction against all government agencies on working with social media companies to censor politically unfavored speech. Citing “substantial evidence” of government’s “dystopian” violations of the First Amendment, Judge Doughty prohibited the federal government from “encouraging, pressuring, or inducing in any manner the removal, deletion, suppression, or reduction of content containing protected free speech.” The injunction not only includes the HHS agencies censoring COVID information, but also the FBI, the Cybersecurity and Infrastructure Security Agency, the State Department, the DOJ, and the White House censoring all forms of protected speech.
This ruling comes a week after the House Judiciary committee produced a preliminary report showing DHS’ CISA was behind the censorship enterprise. It turns out that CISA funded a nonprofit group to work with social media on a process, known as “switchboarding,” which would “trigger content moderation” to “ensure priority treatment of misinformation reports.”
Republicans seem united in combating this censorship and plan to include provisions in the relevant appropriations bills for fiscal year 2024 to block funding for these surveillance and censorship programs. However, where is the same degree of outrage about the dangers of the vaccines themselves?
We now have over two years of information showing ubiquitous injury stemming from damage to all parts of the body, particularly cardiac and neurological. Whether it’s VAERS, European data, countless independent studies, epidemiological data, excess deaths and “died suddenly” mysteries correlating with the take-up of the vaccines, health insurance data, life insurance data, or disability data – we have enough evidence to convict this shot for murder if it were a human standing for trial. Yet not only have these vaccines not been defunded, the same framework that rushed their approval has already been used for countless other new vaccines.
The government’s new shell game is to concede the existence of these problems, but play semantics with the term “rare” when describing their risk. Science Insider published a piece acknowledging the “rare link between coronavirus vaccines and Long Covid–like illness,” including blood clotting, heart inflammation, and neurological disorders. Even Peter Marks, the man at the center of Operation Warp Speed, admitted, “We can’t rule out rare cases.”
“If a provider has somebody in front of them, they may want to take seriously the concept [of] a vaccine side effect,” admits the director of the FDA’s Center for Biologics Evaluation and Research, two years after emails show he ignored concerns of rushing the vaccine amidst a pileup of adverse event reporting.
However, what is rare? The CDC’s own pharmacovigilance program showed a 7.7% rate of clinical-level injury. Coupled with the underreporting rate in VAERS, there were likely millions of severe and long-term injuries, including several hundred thousand deaths in the U.S. So yes, we can suggest that 92% of people didn’t experience clinical levels of injury and 98%-99% didn’t experience long-term and deadly injuries. In that sense, I guess you can say it’s rare. But how many people are we talking about when 5.5 billion people were given at least one dose? Potentially, millions of deaths and hundreds of millions of injuries! Just consider the fact that 25% of injuries reported to VAERS and about a third reported by the European Medicines Agency are considered serious, well beyond the standard of 15%.
House Republicans can no longer ignore the problem with the vaccines. They must also stop ignoring the endless approvals of monkeypox and RSV shots based on dubious data and the same rushed framework. To that end, Speaker McCarthy should take the following actions.
- Defund all COVID shots in the HHS, DOD, and FDA funding bills.
- Create a commission of members of Congress to examine the rationale, safety, and efficacy data of all vaccines, beginning with the new ones recently approved and in the pipeline.
- Refuse to sign off on the Senate version of the Pandemic and All-Hazards Preparedness Act unless major reforms are enacted curtailing pandemic authorities.
- Bar any involvement in a WHO pandemic treaty or expansion of the International Health Regulations.
- Repeal immunity for vaccine manufacturers, including the provision in the 21st Century Cures Act of 2016 that extends the immunity to vaccines offered to pregnant women.
To this day, we still can’t get Republicans to shake their support for the V-word even in red states. Last week, Ohio Gov. Mike DeWine, the consummate COVID fascist governor, used his line-item veto to strike a provision from the budget ending vaccine mandates in colleges. “University and college dormitories and student housing are congregate settings where such policy may be of great importance to ensure resident safety,” said DeWine of vaccine mandates in his veto message. It takes a new level of cognitive dissonance to support mandates on those who don’t want the shot out of fear of harming those who did supposedly get the protection that evidently fails to protect unless the other person gets it!
Republicans all agree that our government engaged in an unprecedented operation to cover up the truth about vaccines. How come their curiosity stops at the degree of exposing the cover-up with no interest in delving into what exactly they are trying to cover up? After all, this is the only product that automatically goes into every arm of every baby multiple times after birth with a set schedule mandated by schools. Certainly the COVID shots are proven to be poison, but is there no interest in uncovering the broader truth?
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Lancet Study on Covid Vaccine Autopsies Finds 74% Were Caused by Vaccine – Journal Removes Study Within 24 Hours
BY WILL JONES | THE DAILY SCEPTIC | JULY 6, 2023
A Lancet review of 325 autopsies after Covid vaccination found that 74% of the deaths were caused by the vaccine – but the journal removed the study within 24 hours.
The study, a pre-print that was awaiting peer-review, is written by leading cardiologist Dr. Peter McCullough, Yale epidemiologist Dr. Harvey Risch and their colleagues at the Wellness Company and was published online on Wednesday on the pre-print site of the prestigious medical journal.
However, less than 24 hours later, the study was removed and a note appeared stating: “This preprint has been removed by Preprints with the Lancet because the study’s conclusions are not supported by the study methodology.” While the study had not undergone any part of the peer-review process, the note implies it fell foul of “screening criteria”.
The original study abstract can be found in the Internet Archive. It reads (with my emphasis added):
Background: The rapid development and widespread deployment of COVID-19 vaccines, combined with a high number of adverse event reports, have led to concerns over possible mechanisms of injury including systemic lipid nanoparticle (LNP) and mRNA distribution, spike protein-associated tissue damage, thrombogenicity, immune system dysfunction and carcinogenicity. The aim of this systematic review is to investigate possible causal links between COVID-19 vaccine administration and death using autopsies and post-mortem analysis.
Methods: We searched for all published autopsy and necropsy reports relating to COVID-19 vaccination up until May 18th, 2023. We initially identified 678 studies and, after screening for our inclusion criteria, included 44 papers that contained 325 autopsy cases and one necropsy case. Three physicians independently reviewed all deaths and determined whether COVID-19 vaccination was the direct cause or contributed significantly to death.
Findings: The most implicated organ system in COVID-19 vaccine-associated death was the cardiovascular system (53%), followed by the hematological system (17%), the respiratory system (8%) and multiple organ systems (7%). Three or more organ systems were affected in 21 cases. The mean time from vaccination to death was 14.3 days. Most deaths occurred within a week from last vaccine administration. A total of 240 deaths (73.9%) were independently adjudicated as directly due to or significantly contributed to by COVID-19 vaccination.
Interpretation: The consistency seen among cases in this review with known COVID-19 vaccine adverse events, their mechanisms and related excess death, coupled with autopsy confirmation and physician-led death adjudication, suggests there is a high likelihood of a causal link between COVID-19 vaccines and death in most cases. Further urgent investigation is required for the purpose of clarifying our findings.
The full study does not appear to have been saved in the Internet Archive, but can be read here.
Without further detail from the Lancet staff who removed the paper it is hard to know what substance the claim that the conclusions are not supported by the methodology really has. A number of the authors of the paper are at the top of their fields so it is hard to imagine that the methodology of their review was really so poor that it warranted removal at initial screening rather than being subject to full critical appraisal. It smacks instead of raw censorship of a paper that failed to toe the official line. Keep in mind that the CDC has not yet acknowledged a single death being caused by the Covid vaccines. Autopsy evidence demonstrating otherwise is clearly not what the U.S. public health establishment wants to hear.
Dr. Clare Craig, a pathologist and co-Chair of the HART pandemic advisory group, says that in her view the approach taken in the study is sound. She told the Daily Sceptic:
The VAERS system [of vaccine adverse event reporting] is designed to alert to potential harms without necessarily being the best way of measuring the extent of those harms.
Quantifying the impact of deaths can be done by looking at overall mortality rates in a country.
However, this is imperfect as a deficit of deaths would be expected after a period of excess deaths, making the accuracy of any baseline dubious.
An alternative approach of auditing such deaths through autopsy is sound.
There may be a bias [in the study] towards reporting the autopsies of deaths where there was evidence of causation and the likelihood of causation might be exaggerated by that bias. For example, 19 of the 325 deaths were due to vaccine-induced immune thrombocytopenia and thrombosis (VITT) but these reports may be overrepresented because of the regulators’ willingness to acknowledge such deaths.
Nevertheless, it is important that attempts are made to quantify the risk of harm and censorship of these attempts, rather than open scientific critique, does nothing to help reassure people.
Walensky Warns Public to Beware of ‘Misinformation’ and ‘Politicized Science’
By Brenda Baletti, Ph.D. | The Defender | July 5, 2023
As she ended her tenure last week as director of the Centers for Disease Control and Prevention (CDC), Dr. Rochelle Walensky warned the American public to be on guard against “misinformation” and the “politicization of science.”
Walensky told The Wall Street Journal she hopes Americans will make health decisions based on “their own risk assessment and their own personal risks, but not through politics,” emphasizing that public health recommendations also shouldn’t be politicized.
“Ironically, this comes after two-and-a-half years of Walensky misinforming the public and politicising the science,” investigative journalist Maryanne Demasi, Ph.D., wrote on her Substack.
Demasi and many others took to Twitter to remind people of Walensky’s false statements and politicized decision-making.
Walensky last week published a farewell op-ed in The New York Times, in which she wrote that public health is critically important in the U.S., and yet she “fear[s] the despair from the pandemic is fading too quickly from our memories.”
She complained that “the agency [CDC] has been sidelined, chastened by early missteps with Covid and battered by persistent scrutiny.”
She also told the WSJ that public health shouldn’t fall along partisan lines.
Yet stark political partisanship defined her time at the CDC. The WSJ reported that a recent KFF poll showed political affiliation was the strongest demographic predictor of COVID-19 vaccination. And about one-quarter of Americans don’t trust the CDC’s health recommendations, according to a 2022 survey published in the journal Health Affairs.
Walensky acknowledged “missteps in communicating” by the CDC, which, she said, “could have done a better job” making it clear to the public that the agency’s message could change during the pandemic.
But, she told the WSJ, the CDC has a plan to regain public trust in the future — by working directly with media organizations to discuss how to best shape public opinion prior to releasing scientific information to the public.
She said the CDC plans to use a method called “prebunking,” where they will communicate directly with media organizations before they release information to let the media know which details about public health might be “misconstrued.”
According to The Associated Press (AP) “prebunking” by public health agencies allows the agencies to define something as “misinformation” before readers have an opportunity to encounter it elsewhere as possibly true.
Then search engines such as Google prioritize “credible websites” like the U.S. Food and Drug Administration’s (FDA) or the CDC’s in its searches.
FDA Commissioner Robert Califf, the Virality Project and Google are among those who have promoted prebunking as a way to combat misinformation.
Journalist Kim Iversen proposed a different approach Walensky might take to restoring public trust in the CDC.
She said:
“Well, the way to do it is to apologize, to own up to your lies, to own up to the mistakes that you made and to discuss why you did that, why the agency followed such political partisanship when they should have been following science, why they ignored the science that was right in front of them.”
CDC broadcast a long list of ‘misinformation’ during Walensky’s tenure
Throughout her tenure at the CDC, which began when Biden took office in January 2021, Walensky made a series of public statements that have proven to be false.
Evidence has since emerged that Walensky knew many of these statements were false when she made them.
In March 2021, Walensky famously told Rachel Maddow, that “vaccinated people do not carry the virus, don’t get sick.”
The CDC was forced to walk back her statements a few days later. But that message was the basis for vaccine mandates imposed later that year by the Biden administration, businesses, universities and public venues throughout the country.
In a mid-June congressional hearing, Walensky defended her March statements, claiming they were true at the time.
But the Washington Examiner reported on June 20 that emails obtained through a Freedom of Information Act request showed Walensky and Dr. Francis Collins were aware of and discussed “breakthrough cases” of COVID-19 in January 2021 — just before the vaccines became widely available — and yet continued to tell the public the vaccines would prevent transmission.
In that same congressional testimony, Walensky also defended the mask mandates, saying that the summary of Cochrane’s review — which found wearing masks in the community “probably makes little to no difference” in preventing viral transmission — had been “retracted.”
But it was neither retracted nor had the authors of the review changed the language in the summary, Demasi reported.
In June 2021, Walensky told “Good Morning America” that the risk of myocarditis was extremely rare, and there was overwhelming data the vaccines were safe for children — even after hundreds of cases of myocarditis had been reported and the CDC had been aware of a safety signal since February.
Under Walensky, the CDC also gave false information on vaccine safety monitoring, added the COVID-19 vaccines to the childhood vaccine schedule despite known harms, withheld data on boosters from the agency’s own advisers and told pregnant women the vaccine was safe — just days after Pfizer reportedly finalized a report demonstrating it wasn’t.
In a March study by Krohnert and others, researchers compiled instances of errors in data presented by the CDC during the COVID-19 pandemic in publications, press releases, interviews and Twitter. The authors reported 25 instances where the agency under Walensky promoted demonstrably false numbers.
In most (80%) cases, the CDC exaggerated the severity of the pandemic. For example, Walensky gave a briefing on June 23, 2022, during which she claimed COVID-19 was a “top 5 cause of death” in children, which was untrue.
Most recently, the House Select Subcommittee on the Coronavirus Pandemic gave Walensky until July 12 to turn over phone records involving American Federation of Teachers (AFT) President Randi Weingarten. The House is investigating potential political interference on the part of AFT with the CDC’s school reopening recommendations during the COVID-19 pandemic, The Defender reported.
Walensky warns of ‘future threats’
Walensky warned at the end of her Times op-ed:
“I want to remind America: The question is not if there will be another public health threat, but when. The C.D.C. needs public and congressional support if it is going to be prepared to protect you from future threats.”
To take on these “future threats” the Biden administration nominated Dr. Mandy Cohen, an internal medicine physician and former state health secretary of North Carolina, to replace Walensky.
But critics warn Cohen is “a public health COVID authoritarian” who is “fully entrenched in the ‘bio-pharmaceutical complex.’”
Dr. Peter McCullough told The Defender that during the COVID-19 pandemic, Cohen failed to recognize therapeutics and natural immunity, and supported lockdowns, vaccine mandates and masking.
Cohen comes to the CDC from the private sector, where she is executive vice president of Aledade and CEO of Aledade Care Solutions, whose executive leadership and board of directors includes people with connections to the World Economic Forum and the Bill & Melinda Gates Foundation.
Walensky congratulated Cohen on her nomination, describing her as “a respected public health leader who helped North Carolina successfully navigate” COVID-19, and whose “unique experience and accomplished tenure in North Carolina … make her perfectly suited to lead CDC as it moves forward by building on the lessons learned from COVID-19 to create an organization poised to meet public health challenges of the future.”
Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.
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.
Exposed, the multi-billion-dollar illusion of ‘HIV’: Part 1
Readers of TCW will be familiar with Neville Hodgkinson’s critical reporting of the ‘Covid crisis’ since December 2020, notably his expert, science-based informed alarm about the mass ‘vaccine’ rollout, so absent from mainstream coverage. What they may be less aware of is the international storm this former Sunday Times medical and science correspondent created in the 1990s by reporting a scientific challenge to the ‘HIV’ theory of Aids, presaging the hostile response to science critics of Covid today. In this series, written exclusively for TCW, he details findings that form the substance of his newly updated and expanded book, How HIV/Aids Set the Stage for the Covid Crisis, on the controversy. It is available here.
By Neville Hodgkinson | TCW Defending Freedom | July 3, 2023
Three years into the Covid crisis, many are now aware of the disastrous advice on which so many governments blindly acted. False predictions of spread, fearmongering propaganda, lockdowns damaging young and old, suppression of cheap treatments to make way for a dangerous, experimental vaccine . . . so much of ‘the science’ turned out to be fiction, hugely profitable for a few but harmful for billions.
These failures have brought back into focus claims that the syndrome known as HIV/Aids was – and still is – being similarly mishandled and exploited by the worlds of medical science, public health and Big Pharma. Robert Kennedy Jr documents this in detail his best-selling 2021 book The Real Anthony Fauci: Bill Gates, Big Pharma, and the Global War on Democracy and Public Health.
What few people know however is that for almost 40 years a small group of scientists has deconstructed almost every aspect of the theory that Aids is caused by a lethal, sexually transmitted virus known as HIV. Their critique goes beyond questioning HIV as the cause of Aids. They say ‘HIV’ has never even been proved to exist. And the reason you have probably never heard of their work is that, like the doctors and scientists who challenged Covid insanities, they have been silenced at every turn.
With Covid, pressure to conform came through government-directed appeals to our higher nature through slogans such as ‘Stay at home. Protect the NHS. Save Lives’ and ‘Every vaccination gives us hope’. The implied claim was that anyone who thought differently was either an idiot or a murderer.
Similarly with Aids, advocates of the deadly virus theory sought to make those who questioned it sound as though they were lacking in compassion, irresponsible or stupid.
I was working as medical correspondent of the London Sunday Times in the 1980s when Aids suddenly became big news after American government scientists claimed to have identified a previously unknown virus as the cause of a mysterious cluster of symptoms related to severely depleted immunity. They included Kaposi’s sarcoma, a cancer affecting the skin and internal organs; severe candidiasis; and pneumonia caused by an out-of-control fungus. The symptoms proved resistant to treatment, and fatal in a number of cases.
The first victims were groups of gay men who were challenging long-standing homophobic attitudes in American society through what came to be known as the ‘fast-track’ gay lifestyle. This involved multiple sex partners and heavy drug use.
The partying was fun, I was later told, but it caused disease microbes to become pooled among participants such that almost every encounter carried a risk of infection. Prophylactic use of antibiotics staved off some illnesses but contributed to an underlying deterioration, and in some cases complete collapse, of the immune system.
The crisis at first met an unsympathetic response from the right-wing Reagan administration. The common histories of the victims led to dismissive descriptions of Aids as a ‘gay plague’. As numbers increased, however, outrage and anger grew. Those involved had often already suffered greatly from discriminatory attitudes and behaviour, and their efforts to end this bigotry through the Gay Lib movement looked to be under threat.
That was the context in which US biomedical researcher Robert Gallo found immediate acceptance when in 1984 he claimed to have identified a deadly virus, new to humanity, as the cause of Aids. The theory took off like wildfire and by the end of 1984 had come to be accepted by virtually everyone. The microbe Gallo said he had found became known as the Human Immunodeficiency Virus, or HIV.
It brought virologists, drug companies and public health experts to centre stage. Taxpayer dollars, eventually reaching hundreds of billions, were poured into Aids research and treatment through the US National Institutes of Health, in particular the National Institute of Allergy and Infectious Diseases (NIAID) under the leadership of Dr Anthony Fauci. Well-funded NGOs and activist groups sprang up with the aim of contributing to the fight against the disease.
Religious leaders warmed to the theory because it discouraged sleeping around. Politicians liked it because it put in place a new ‘enemy within’ against which they could claim to offer protection with advertising campaigns such as the UK’s ‘Aids: Don’t Die of Ignorance’ – a precursor of the intense propaganda inflicted on us with the advent of Covid-19.
Media people – including me, I am ashamed to say – vigorously promulgated warnings that the virus put at risk everyone and anyone who had sex. It felt good to be not just selling newspapers, but helping to sound the alert.
Young people were less readily taken in. James Delingpole has recalled how the ad campaign put a dampener on his sex life, though after the initial shock it became increasingly clear to him that the government had been overstating the case.
In fact, as the late Nobel Prize-winning chemist Kary Mullis and other scientists were to point out, there never was a body of scientific evidence demonstrating the validity of the ‘deadly new virus’ idea. That remains the case today, despite hundreds of thousands of papers having been published over the years predicated on the HIV belief system.
Henry Bauer, a retired professor of science studies who has drawn on numerous sources in documenting The Case Against HIV, says: ‘Anyone open to looking at the actual data . . . can find an enormous amount of evidence that the diagnosis of HIV as cause of AIDS is simply wrong.’
One lasting outcome of the theory was that by ‘democratising’ Aids, with the message that the disease did not discriminate and so everyone was at risk, it prevented the feared setbacks for the Gay Lib movement. Lesbian and gay rights became firmly established in American society, and in some other parts of the world.
In many other ways, however, the global hysteria to which the theory gave rise has had disastrous consequences, some of which continue to this day.
A failed cancer drug called AZT, pulled off the shelf by American government researchers because of an apparent anti-HIV effect, killed and injured thousands. It was administered in high doses not just to people with Aids but to gay men, haemophiliacs and others thought to be HIV-infected, earning hundreds of millions of pounds for the US drug company Burroughs Wellcome and its British parent, the Wellcome Foundation (later taken over by Glaxo). American and British government institutions promoted it vigorously as the ‘gold standard’ of Aids treatment. Doctors who stepped publicly out of line were hounded out of the profession.
Although later generations of drugs can genuinely help to support a failing immune system, 40 years of research has failed to bring either a vaccine or cure for the purported ‘HIV’ infection. Taken over long periods, the drugs themselves can kill, contributing significantly to the 800 or so deaths reported annually of ‘people living with HIV’ in the UK.
The most widespread and long-lasting harm, however, has been to the countless people around the world, especially in Africa and of African descent, terrorised with a false belief that they are victims of a sexually transmitted virus which only Western medicine has the means to hold at bay. The World Health Organization (WHO) claims that more than 80million people have been infected, and that about 40million have died from HIV. Three-fifths of purported new HIV infections are said by WHO to be in the African region. African Americans are eight times more likely to be diagnosed with HIV infection compared with the white population.
American taxpayers in particular have been burdened with the huge expense of maintaining an industry that has grown up around HIV/Aids. The US government spends more than $28billion a year on the domestic response, and expenditure globally between 2000 and 2015 totalled more than half a trillion dollars ($562.6billion), according to a University of Washington study. Yet the Joint United Nations Programme on HIV/AIDS (UNAIDS), in a never-ending plea for more money, says the pandemic continues to take a life every minute.
In this series of articles I am going to describe the fruits of years of painstaking work by scientists based in Perth, Western Australia, collating evidence challenging almost every aspect of the ‘HIV’ theory. The essence of their case is that there is no ‘HIV’ epidemic, and there never will be a vaccine or cure, because there is no ‘HIV’.
If you find this hard to believe, I am with you entirely in the sense that it took me years to accept fully how wrong I had been in my early reporting on Aids. I documented this painful journey of discovery in my book AIDS: The Failure of Contemporary Science, published in 1996 by Fourth Estate.
If you ask how it could be possible that for 40 years the scientific and medical worlds have failed to correct a belief in a mythological virus, the answer is more sociological than scientific.
Solidarity with the suffering of the gay community played a part – although genuine kindness, such as Louise Hay demonstrated in her early healing work with people with Aids, strongly and successfully challenged the medical view that they were certain to die. An arrogant, but ill-informed, neocolonial drive by countless NGOs to ‘do good’ in poorer parts of the world also contributed. But probably the most powerful and detrimental element in maintaining the deception was the money and influence involved, as governments went into partnership with the hugely profitable pharmaceutical industry. The resources poured into HIV/Aids created thousands of jobs, buying loyal collaboration and stifling dissent.
Highly experienced scientists who spoke out against the theory were ridiculed, defunded, gaslighted, and accused of killing people by weakening the public health message.
I experienced this pressure myself when I began to examine alternative ways of looking at Aids in the early 1990s, when I was working as Sunday Times science correspondent. Joan Shenton of Meditel, producers of prize-winning but much criticised documentaries on the issue, alerted me to the fact that several distinguished scientists had challenged the idea that HIV could be doing all the damage attributed to it.
Andrew Neil, editor of the Sunday Times, which had serialised Michael Fumento’s 1990 book The Myth of Heterosexual Aids, supported my reports on an ever-deepening scientific challenge to the theory. Over a three-year period, condemnation came from just about every quarter. The deeper the critique went, the shriller the protests became.
In 1993, with the HIV/Aids industry still pointing to Africa as proof of how millions could become infected, Neil told me to go there to find out what was happening. Over six weeks, travelling through Kenya, Zambia, Zimbabwe and Tanzania, it became increasingly plain to me that the entire pandemic was an illusion arising from diseases of poverty being reclassified as ‘HIV/Aids’.
My reports to this effect proved too much for the scientific establishment, and Nature – supposedly one of the top scientific journals in the world – declared that we must be stopped. Having decided that picketing our offices would be impractical, the magazine mounted a campaign of ridicule. The UK’s Health Education Authority started an Aids journalism award specifically in my dishonour. They said it was to counter the newspaper’s dangerously misleading coverage. There was incomprehension and abuse from all three main political parties, as well as from scientific and medical chiefs.
But we also heard from many doctors, health workers, gay men, and specialists on Africa, thanking the newspaper for its challenging coverage. An ‘HIV’ diagnosis at that time could still have the power of a witch-doctor’s hex, and people who had tested positive wrote to say that our reports were like a breath of fresh air.
Andrew Neil was undeterred by the hostile bluster, while insisting the paper was ready to publish any evidence that countered the dissident case we were presenting. In 1994 he left the paper for New York, and I left too after his successor John Witherow made it plain that he did not want me to continue this line of reporting. The literary agent David Godwin had been in touch, suggesting a book on the controversy, and this took shape over the following year.
When Fourth Estate published it in 1996, however, it became an early victim of ‘cancel culture’. The late American gay activist Larry Kramer, at first a bitter critic of Fauci but later his friend and ally, was in the UK at the time of publication to address a conference on Aids. He picked up a copy at a pre-conference gathering, tore several pages, and spat in it, telling his audience: ‘Do the same if you come across this book. They will soon stop stocking it.’ It quickly disappeared from view, subsequently topping a list of ‘Books You’re Not Supposed to Read’ in a work on political incorrectness in science.
(From The Politically Incorrect Guide to Science, by Tom Bethell, Regnery, 2005)
I am republishing it now, with additional material including a summary of where the science of ‘HIV’ went wrong, because the story is so redolent of the misunderstandings, mishandling and downright lies surrounding Covid-19. As with Aids, huge grants from Big Pharma and ‘philanthropic’ foundations to researchers, medical associations, consumer groups, and civil rights organisations fuelled the Covid illusions.
There is one important difference. At first I thought the Covid fearmongering was as ill-conceived as that over ‘HIV’ and Aids. It soon became clear, however, that unlike ‘HIV’ this was a genuine pathogen. A disgracefully suppressed paper by the UK’s Professor Angus Dalgleish, working with Norwegian colleagues including a biowarfare expert, demonstrated beyond reasonable doubt the genetically-engineered nature of SARS-CoV-2 (see here and here).
Panic measures to try to hide its laboratory origin confirm that view. These were led by the Chinese, from whose Wuhan laboratory the virus almost certainly escaped, and by Fauci, whose NIAID had part-funded the work. Sir Jeremy Farrar, then director of the UK’s Wellcome Trust and now WHO chief scientist, also played a leading role in the cover-up.
Many are now aware of the adverse social, economic and health consequences of the Covid hysteria into which Fauci and others led us. Billions of people meekly accepted and even welcomed unprecedented lockdowns and other fearmongering measures, along with mass administration of the mRNA gene products. TCW Defending Freedom has been one of few voices constantly critical of the mishandling of Covid over the past three years, despite high-level, far-reaching efforts to silence and defund the site.
Much less widely understood is the way Aids became subject to similar mismanagement 40 years ago, with adverse consequences lasting until today.
Laid Low by the COVID Vaccine, Now They’ve Got a Bad Case of Federal Unresponsiveness
By Christian Britschgi | RealClear Investigations | June 28, 2023
In April 2021, Adele Fox received a single shot of the Johnson & Johnson COVID-19 vaccine. Within a few hours, the 60-year-old resident of Portsmouth, New Hampshire, started feeling shooting pains in her legs, arms, and neck. The pain didn’t abate over the next few days. Instead, it got worse and was accompanied by nausea and debilitating fatigue.
Within a few weeks, neurologists affiliated with Massachusetts General Hospital diagnosed her with several serious conditions they say were a result of her COVID-19 vaccine, including small-fiber neuropathy (which causes a painful tingling in the extremities) and Sjögren’s Syndrome (which leaves patients pained and fatigued, and in extreme cases, can damage internal organs).
This shot, which was supposed to get Fox back to normal, instead left her with diminished ability to work and enjoy life. Persistent physical therapy and experimental treatments she’s taken since have done little to alleviate her symptoms.
“I used to do so much, and now it’s a struggle,” she says. “Sometimes you just get down.”
With her medical bills mounting and her condition not improving, Fox sought compensation for her damaged health. Federal liability protections prevent the vaccine-injured from directly suing vaccine manufacturers like Johnson & Johnson. Instead, claimants have to go to the federal government for compensation.
But as Fox would soon learn, the government has two starkly different injury programs for vaccines. One operates like a civil court with a neutral judge, lawyers on both sides, and a guaranteed right of appeal. In recent decades, it has approved about 75% of claims and pays out hundreds of millions of dollars per year.
The other, which handles COVID-19 vaccines, has rejected almost every claim brought to it, awarding less than $10,000 since the pandemic. And in a nation nearly numb to the pandemic’s toll and its scandals, the program is adding seething frustration atop lasting injury to Fox and people like her in a little reported aftermath to the government’s much criticized performance on vaccines – ranging from erratic booster advice to broad-brush vaccine mandates that cost people their jobs.
Fox filed her claim two years ago, submitting hundreds of pages of medical documents about her condition and diagnoses. She’s nevertheless one of the 10,887 people still waiting on a decision. “You’re not even hearing anything from the organization that’s supposed be helping you,” she says. “The phone keeps ringing, no one is emailing, nobody is doing anything.”
The federal agency overseeing the program, the Health Resources and Services Administration, said in a statement to RealClearInvestigations that the current number of claims “significantly exceeds the previous volume in the program” and that the program has “hired additional staff to address this growth in claims, and the President’s budget requests additional funding to support the additional staffing needed to process claims.”
Tale of Two Compensation Programs
The government’s two contrasting vaccine compensation programs are similarly named and thus easily confused. The first, Vaccine Injury Compensation Program (VICP) was created in the 1980s and covers most routine vaccines. The second, the Countermeasures Injury Compensation Program (CICP), is a result of war-on-terror legislation in 2005 and now covers COVID-19 vaccines. Their bureaucratic differences help explain why a nation that has spent trillions of dollars on COVID relief programs has provided almost no assistance to people harmed by the vaccines that the government encouraged, and sometimes required, them to take.
The earlier program was supposed to shore up pharmaceutical companies’ willingness to make childhood vaccines in the face of persistent vaccine injury lawsuits, while also giving the vaccine-injured a fair and expedited process for compensation.
The vaccine-injured would not sue pharmaceutical companies. Instead, they’d petition the government in Federal Claims Court, where special masters (judges) would decide cases. Compensation came from a government-administered trust fund paid for by excise taxes levied on vaccine manufacturers.
Between 2006 and 2021, this court adjudicated cases from 10,602 petitioners and issued compensation to 7,618 of them. The compensation trust fund sits at $4 billion and pays out about $200 million in compensation and attorneys’ fees each year.
This earlier program bears little resemblance to the Countermeasures Injury Compensation Program, where the COVID-vaccine cases of Fox and many others are languishing.
It was meant to incentivize pharmaceutical companies to be part of the federal response to one-off, one-in-a-million events like a bioweapon attack or an outbreak of a deadly pandemic. Although almost one billion doses of COVID-19 vaccines have been administered in the United States, and health authorities say boosters could become as common as the annual flu shot, it remains the only way people harmed by the shot can receive compensation.
It’s far from guaranteed they’ll get it.
Before the pandemic, this program received a little over 500 claims and had paid out compensation to only 30 people – mostly for H1N1 (swine flu) vaccine injuries. In just the past two years, it has been asked to make decisions on over 10,000 injury claims related to COVID countermeasures.
As of June, it made decisions on just 919 of these COVID-related claims and rejected 894 of them. It has so far paid out only $8,593 in compensation to just four people who were injured by a COVID vaccine. The program has deemed another 20 people eligible for compensation, but has yet to pay them.
It’s not a judicial process either. Rather, it’s an administrative process overseen by Health Resources and Services Administration, which is housed within Department of Health and Human Services (HHS). People file a claim and government medical reviewers decide whether to pay out or not. That’s an awkward arrangement, given that HHS is deciding whether to pay for damages caused by products it approved and in some cases mandated.
Because it’s an administrative process, there’s no right to counsel and no neutral arbitrator. A denied claimant can file for reconsideration with HRSA, but otherwise has no right to appeal.
Unlike the earlier program, the CICP offers no compensation for pain and suffering and doesn’t pay attorneys’ fees. Most successful claimants have received compensation totaling a few hundred dollars or a few thousand dollars. The highest award for a COVID-19 vaccine injury sufferer was $3,957.66 to a person who got myocarditis (a heart condition) from a vaccine.
It also has shorter filing deadlines. People have to file a claim within one year of vaccination, a much shorter window than the earlier program’s standard of three years from the onset of symptoms. Of the 894 claims that CICP has rejected, 444 of them were for missing the filing deadline.
CICP also only awards compensation in cases where there’s “compelling, reliable, valid, medical, and scientific evidence” that someone’s injury is linked to a covered countermeasure. HRSA describes this as “a high evidentiary standard.” Renée Gentry, a practicing vaccine injury lawyer who directs the Vaccine Injury Litigation Clinic at George Washington University, says it’s a much higher bar than what the earlier vaccine injury compensation program requires, which contributes to a much lower rate of successful claims.
The Countermeasures Injury Compensation Program’s nature as a small emergency program has seen its capacity strained by a flood of COVID-related injury claims. Of the 11,806 COVID-related claims filed, 10,887 are still pending. Those four cases where COVID compensation was paid out didn’t come until after April 2023, over two years since the first vaccines were administered.
Pain and Suffering
The shortcomings of CICP are all too apparent for the people who are forced to wade through it. Even folks who seem to have done everything right are left waiting or disappointed by the program.
Fox filed her claim in May 2021, which was relatively early in the immunization campaign. She also had clear diagnoses from well-credentialed doctors linking her conditions to her COVID-19 vaccination. Fox says she provided the program with no shortage of documentation as well.
After filing all that paperwork, she hasn’t been idle either. After months of not hearing anything back from CICP, Fox started to reach out repeatedly to anyone she thought might be able to move the needle. She spoke repeatedly with representatives from Sen. Jeanne Shaheen’s and Rep. Chris Pappas’ offices. She also kept calling program administrators, trying to figure out what was taking so long.
“I’m sure they saw my number, and said ‘Ah, Fox, oh no, not her [again]’,” she jokes.
Her congressional representatives did reach out to CICP on her behalf. That was at least effective at getting program administrators to call Fox personally twice, once in July 2022 and again in June 2023. But each time, they could only offer her reassurance that her paperwork had been received. On both calls, Fox says she was told that the program was vastly overburdened by the flood of COVID-19 claims it had received. She, like thousands of others, would have to wait.
The few decisions on COVID-19 claims that have trickled out haven’t offered much relief to the people who’ve received them. That includes Cody Flint, one of the 894 people who’ve had their COVID-related claims rejected.
Flint was vaccinated in February 2021, when he received a single Pfizer dose. He says that he started to feel headaches and had affected vision within 30 minutes of the shot. He was still experiencing symptoms two days later when he headed to his job as a crop-dusting pilot.
While flying that day, he started to experience extreme tunnel vision, followed by a sensation he describes as “a bomb [going] off in my head.” He barely managed to get his plane back to his runway, where his coworkers found him slumped over his controls and shaking.
He was diagnosed with perilymphatic fistula (or tear of the inner ear) caused by elevated intracranial pressure – which could only be relieved through repeated draining of his spinal fluid. Given the timing of his symptoms and the fact that he’d passed a flight physical just a couple weeks prior, his doctors said his condition was almost certainly caused by the vaccine. His injury prevented him from returning to work as a pilot, and his mounting medical bills saw him draw down all of his savings.
In April 2021, Flint filed a claim. In May 2022 – just a few weeks after Sen. Cindy Hyde-Smith asked HHS Secretary Xavier Becerra about his case specifically in a committee hearing – Flint’s claim was rejected. The program’s medical reviewers told Flint that it was more likely his injuries were caused by barotrauma from flying a plane.
He petitioned for a reconsideration of his case. His doctors argued that there was no way he’d have experienced barotrauma from flying just a few hundred feet off the ground. Commercial airliners, they noted, are pressurized at 6,000 to 8,000 feet of elevation. Flint’s lawyers also submitted recent studies linking the symptoms he’d experienced to COVID-19 vaccinations.
Nevertheless, a separate medical reviewer at HRSA upheld the CICP’s initial denial in January 2023. That letter succinctly stated that HHS has “no appeals process beyond this reconsideration” and “there is no judicial review of a final action concerning CICP eligibility.”
Efforts at Reform
The federal government’s liability protections for COVID-19 vaccines aren’t scheduled to expire until the end of 2024. Once they do, those claiming a vaccine injury will be able to pursue claims against vaccine manufacturers in state courts.
While liability protections remain in effect, the federal program is injured claimants’ only potential source of compensation.
Whether or not the HRSA succeeds in boosting staffing in line with its statement to RCI, those seeking compensation have started to get organized. They’ve formed the group React19, which is dedicated to advocating for additional research into the side effects of COVID-19 vaccines. It’s grown into a network of tens of thousands of people who say they suffered adverse injuries from the shot. Flint, the pilot, is on its board of directors.
“It’s a very pro-vaccine community,” says Christopher Dreisbach, the group’s legal affairs director. “You say anything about vaccine injuries, you’re branded as anti-vaxxers. We are pro-science, we are not political. We’re just dealing with a very politicized issue.”
He says the politicization of vaccines has made their efforts at compensation reform a challenge.
When the CICP, and the 2005 Pandemic Response and Emergency Preparedness (PREP) Act that created it, were first being debated, Republican lawmakers were its main advocates, while its main critics were Democrats. The partisan politics of the program and liability protections for pharmaceutical companies has done a 180 since COVID.
In 2005, Rep. Sheila Jackson Lee argued during the House floor debate on the PREP Act that the law’s liability shield would leave injured healthcare workers with little protection or chance of compensation. Come 2023, she would return to the floor of the House to argue in favor of mandating those same healthcare workers receive a vaccine covered by the PREP Act’s liability shield.
The PREP Act’s harshest critics during COVID, meanwhile, have mostly been Republicans.
“I call the PREP Act medical malpractice martial law,” says Rep. Thomas Massie, who complains that its liability shield is both incredibly broad and improperly preempts state law. “I think it’s sort of anathema to the way our government is set up. I found it hard to believe that Congress would pass something, much less that a Republican president would invoke it.”
In March 2022, Sen. Mike Lee introduced a bill that would have amended CICP to give claimants the same framework for pursuing compensation as the VICP. They could file in Federal Claims Court and receive an expedited, judicial adjudication of their injury claim.
Gentry argues that it would be far simpler to just move the COVID-19 vaccines into the VICP program, which already has a successful track record of adjudicating injury claims. In order for that to happen under the law that created the VICP, the CDC needs to recommend the vaccines for routine administration to children (which has already happened) and vaccine manufacturers would have to start paying excise taxes. That latter condition will require action from Congress.
VICP needs a number of updates as well, says Gentry, including expanding the number of special masters to handle the backlog of cases and increasing the available levels of compensation (which haven’t been updated since the 1980s).
Increasing the number of special masters is particularly important if the VICP program is going to be expected to process tens of thousands of COVID claims, she says. But she argues it’s the best way of getting the vaccine injured out of CICP and into a program that will work for them. “If you’re taking away someone’s constitutional right to sue, you really have to give them a reasonable and meaningful alternative and that’s what this program is, for all of its faults,” says Gentry.
While efforts at reform in Washington lumber on, React19 has started a privately funded compensation program that’s thus far paid out $552,000.
“Is that making a meaningful difference to all the vaccine injured everywhere? No, that’s not enough,” says Dreisbach, but he notes that it’s far more than what CICP has paid out. “That should be pretty embarrassing to the federal government.”
Government Contracts With COVID Vaccine Makers Let Federal Agencies Bypass Normal Regulatory Process: FOIA Docs
By Brenda Baletti, Ph.D. | The Defender | June 30, 2023
A little-known federal agency called BARDA dedicated to countering “health security threats” was responsible for conducting the quality review of every COVID-19 vaccine dose administered in the U.S., Sasha Latypova reported on her Substack.
But BARDA, the Biomedical Advanced Research and Development Authority, which has a “militarized” purpose according to Latypova, is not subject to the same regulations as typical pharmaceutical manufacturers, distributors or regulatory agencies.
Distribution through BARDA was part of the “bait and switch” the federal government subjected the American people to with the COVID-19 vaccines, Latypova — a former pharmaceutical industry executive who now exposes fraud in COVID-19 countermeasures — told The Defender in an interview.
“The public was told these vaccines are made by Pfizer and Moderna and rigorously approved by the FDA.” That, she said, would mean that the “consumer protections we expect from pharmaceutical products, medical devices and even food — which are huge and extensive — we expect them to be in place.”
But in fact, countermeasures contracts made available through Freedom of Information Act (FOIA) requests by various parties and U.S. Securities and Exchange Commission disclosures show the U.S. Department of Defense (DOD) and BARDA contracts with the pharmaceutical companies were structured such that these protections weren’t required, according to Latypova.
The contracts also specified that manufacturers and federal agencies were protected by the Public Readiness and Emergency Preparedness (PREP) Act, which shields “covered persons” — such as pharmaceutical companies, or the DOD/BARDA — from liability for injuries sustained from “countermeasures,” such as vaccines and medications administered during a public health emergency.
Latypova posted a video of a November 2022 presentation during which BARDA’s then-director of Regulatory and Quality Affairs (RQA) Tremel Faison bragged that before the U.S. government could purchase and release any COVID-19 product, the RQA team had to perform a review and acceptance.
“I thought it was very strange, given that this is technically the FDA’s [U.S. Food and Drug Administration] job,” Latypova wrote, so she investigated BARDA.
BARDA is housed within the U.S. Department of Health and Human Services, but its purpose is “to develop medical countermeasures that address the public health and medical consequences of chemical, biological, radiological, and nuclear (CBRN) accidents, incidents and attacks, pandemic influenza, and emerging infectious diseases.”
BARDA now functions as part of the Office of the Assistant Secretary for Pandemic Preparedness and Response, elevated by the Biden administration in 2022 to coordinate the nation’s response to health emergencies.
BARDA reports that it has 77 products on the market.
This is concerning, Latypova said, because typically pharmaceutical products are subject to regulations that govern the clinical trial and manufacturing process and then the licensed pharmacy distribution system monitors for consumer safety.
They are subject to “cGxP” regulations, a suite of “current good practice” processes and procedures with the “x” standing in for a variety of life sciences areas, including manufacturing, laboratory, clinical and distribution.
Those regulations create tight control over pharmaceutical products ensuring, for example, that labeling is accurate, dosage is accurate, there are no impurities, and the active ingredients are active and present in the proper amounts.
The regulations also establish supply chain regulations so the products are tracked during transportation and distribution and are traceable, and they protect consumers from drugs being counterfeit, stolen, contaminated or otherwise harmful.
According to Latypova, the fact that BARDA receives and quality checks the vaccines means the vaccines and COVID-19 countermeasures are subject to different protocols than typical FDA-approved or FDA-authorized products.
According to BARDA’s Standard Operating Procedure (SOP) documents outlining its procedures for receiving and inspecting medical countermeasure products, which Children’s Health Defense obtained through a FOIA request, materials ordered by BARDA have their own process of approval.
Products are shipped from the manufacturer to BARDA. Prior to delivery, BARDA receives the lot number and a certification from the producer that says the product meets its established specifications and contains other technical information such as lot number, etc.
BARDA’s RQA team then receives sealed trucks, makes sure documentation is in order and temperature control is maintained, watches the unloading, and “conducts a cursory examination of obvious physical damage.”
BARDA does not test or verify the contents of the vials it receives. It simply accepts the claims in the manufacturers’ paperwork.
And the products from BARDA, according to the SOP, go into storage at a Strategic National Stockpile site, which, unlike typical pharmaceutical storage sites, is also not subject to regulations.
Pharmacy distribution is licensed on a state-by-state basis. Those regulations are typically extensive as seen, for example, in the Pharmacy Lawbook for the state of California that Latypova posted.
It was previously known that the FDA exempted COVID-19 countermeasures from many of these requirements, justifying that exemption based on the public health emergency.
In May, the FDA extended that exemption beyond the May 11 end of the COVID-19 public health emergency.
But the BARDA documents reveal how limited the oversight provided for the receipt and inspection of countermeasures is in practice.
Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.
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.
Can this treatment bring hope to the abandoned vaccine victims?
By Sally Beck | TCW Defending Freedom | June 29, 2023
The unprecedented range and extent of Covid vaccine injury is not open to argument. Yellow Card reporting, which the Medicine and Healthcare products Regulatory Agency say represents just 10 per cent of the true number of reactions, reveals that medical staff and victims have reported half a million adverse events and nearly 2,600 fatalities.
The most common issues following vaccination are low blood platelets (immune thrombocytopenia), heart inflammation (myocarditis), blood clots in the body and brain, (thrombosis and cerebral venous thrombosis) and Guillain-Barré syndrome, where the body attacks its nerves and can cause paralysis.
More than one thousand peer-reviewed research papers have documented and explained the connection between injury and the novel Covid gene therapy; 228 of those papers involve myocarditis, 150 thrombosis, 116 thrombocytopenia, 61 cerebral venous thrombosis, and 43 Guillain-Barré syndrome.
According to the American Vaccine Adverse Events Reporting System (VAERS), who have received 35,302 reports of deaths, the Covid vaccine has led to more death reports than any other vaccine in history. The weight of evidence is startling but many doctors still deny Covid-19 vaccines can cause disability or death.
Despite such unprecedented numbers, our national medicines monitors continue to diminish vaccine injury. Last month the UK Health Security Agency (UKHSA) published this 51-page report on the Covid-19 vaccine programme for healthcare professionals which still describes vaccine injury as rare or of little significance. With no official recognition, there is no government investment into research to understand the pathology of vaccine injury, and no treatment trials to help the millions of vaccine injured.
Former scaffolder Alex Mitchell, 59, from Glasgow, nearly died of vaccine-induced thrombotic thrombocytopenia (VITT) officially caused by the AstraZeneca vaccine which he received on March 20, 2021. He developed blood clots so severe that his left leg was amputated above the knee. A range of medication controls his continuing clotting problems, but Alex, who has been called a liar, conspiracy theorist and anti-vaxxer, despite his official diagnosis and £120,000 compensation payment, has found more help to deal with his ongoing health issues through social media than he has through the NHS.
He said: ‘Supplements were recommended by someone who contacted me on Twitter who has a degree in chemistry and biology. My energy and the fatigue that us vaccine-injured suffer from has improved since I started taking them six months ago.
‘The other things that help are acupuncture and red light therapy. They reduce inflammation, and the severe muscle spasms I was experiencing, which felt like someone had taken a cattle prod to my heel bone, have almost stopped.’
A few dedicated doctors are listening and are raising funds for independent research. One is the US organisation Frontline Covid-19 Critical Care Alliance (FLCCC) founded by a number of doctors including Dr Pierre Kory, and Children’s Health Defence Europe, who held a conference with Dr Meryl Nass last month to discuss vaccine injury.
FLCCC is at the forefront of developing protocols to help the vaccine injured. It is spearheaded by Professor Paul E Marik, formerly chair of pulmonary and critical care at the Eastern Virginia Medical School. He talks regularly to practitioners from all over the world via phone or Zoom who share their clinical experiences. Nothing is added to the FLCCC protocols without a high degree of investigation and scientific reference. Their current vaccine injury protocol has more than 700 scientific references.
Their natural healing regime includes the enzyme nattokinase and aspirin to dissolve blood clots; the anti-inflammatory supplement resveratrol; the mineral magnesium which regulates blood pressure, blood sugar, and is needed for good muscle and nerve function; omega-3 fatty acids which regulate blood clotting; energy boosting co-enzyme Q (CoQ10); the sleep-regulating hormone melatonin; bromelain, the pain-reducing enzyme found in pineapple; the plant chemical berberine which helps strengthen heartbeat, and the brain-nourishing amino acid N-acetylcysteine (NAC).
It has had mixed results but one group called ZeroSpike hope they have made a major breakthrough. ZeroSpike was put together by Fabio Zoffi, a tech entrepreneur, who three years ago formed Federazione Rinascimento Italia (FRI), a civil society of Italian doctors, lawyers, scientists, professionals, and entrepreneurs, horrified by the draconian Covid response.
He contacted Dr Loretta Bolgan, a doctor of chemistry and pharmaceutical technology, and asked her to investigate the Sars-CoV-2 virus and the new mRNA vaccine technology. Once the team discovered that the Covid vaccines and the virus both contained the spike protein, Zoffi asked them to develop a way to get rid of it.
The spike contributes to cardiovascular, brain, and blood clotting problems, and can cause autoimmune conditions, cell deformation and cell fusion damage. It can cross the blood-brain barrier causing memory loss and brain fog, can trigger a stroke or cause other neurological issues.
Manufacturers said the injected spike would clear itself naturally but information from the respected pathologist Professor Arne Burkhardt in Germany, who died recently, and from a freedom of information request from Pfizer’s nonclinical evaluation report submitted to the Australian Department of Health, shows it does not and that it can damage major organs, including the ovaries, liver, spleen and adrenal glands.
The team of ten focused on the food supplement NAC which specifically helped the condition which the vaccine injured and those with long Covid describe as brain fog. Studies showed that NAC denaturated (removed) between 12 per cent and 15 per cent of the Covid spike protein.
NAC is derived from the amino acid L-cysteine and helps replenish glutathione levels in the body and can help to improve brain function. Glutathione is produced by the liver and helps with immune system function, as well as tissue building and repair, vital to help the injured recover. The team then used quantum physics to turbo charge – augment – the NAC molecule, which made a huge difference. In the lab (in vitro), they claim it removed 99.8 per cent of extracellular spike, although there are no traditional double-blind placebo-controlled trials to support the claim.
To prove it, the team developed a urine test which showed how much spike was being excreted. Women’s health specialist Dr Tina Peers told the audience at the Better Way conference in Bath this month: ‘If you check someone’s urine before they take augmented-NAC there aren’t the end products of the denaturation, but by day eight of taking it, they found that the urine was full of denatured spike protein.’
Health practitioners with no financial interest in the product are calling it a ‘game-changer’. Pulmonary and critical care specialist Dr Pierre Kory told the Better Way audience: ‘I integrated it into my practice two months ago. Not everybody responds but some testimonials are really earth-shattering.’
Scott Marsland, a registered nurse (RN) since 1997 and a family nurse practitioner (FRP-C) since 2014, is a partner with Dr Kory in a Covid treatment practice in Syracuse, New York. They have treated more than 2,000 Covid, long Covid or vaccine injured patients in the last 14 months.
Marsland is impressed with A-NAC. He said: ‘I have treated 72 patients with it and 75 per cent have noted benefit. Three had adverse responses of mild to severe rash, but that fully resolved quickly.
‘I had a patient with mental health issues, including anxiety and depression. After taking it, he said, “I’m sleeping like a baby. A cloud has lifted.” Another, who suffered spinal injury after a car crash, had very poor respiratory status preventing the operation. Within a week she reported her lungs were stronger than in the last three years. A young patient with 5/10 chest pain reported after three days the pain was measuring 2/10.’
Dr Peers was herself injured by two AstraZeneca vaccines. She said: ‘I had a tremor in my hand, I had dormant mast-cell activation syndrome (MCAS) which flared, my face was puffy, my eyes were swollen. It affected my immune system.’
She began taking augmented NAC more than two months ago and developed a rash, like Marsland’s patients. She said: ‘After a few days I had a detox reaction and developed eczema on my face. It lasted about 48 hours but now my tremor has gone, the rash has gone and my MCAS is under control again.’
In Italy, a country hit by some of the most brutal Covid measures including a ‘no jab, no job’ policy which lasted for 18 months, ZeroSpike have helped more than 10,000 patients. Internationally, they have treated a total of 20,000 patients and say that none has come back with any complaints. Patients will generally complain if they experience negative events.
Can this new treatment give people abandoned by their governments hope? Will the medical establishment engage with this research and its findings? With countries such as Canada already making a move to ban all natural supplements like A-NAC, there will be a huge battle for recognition. But as Alex Mitchell says, ‘They’ll stop us accessing successful treatments over my dead body.’
CISA Was Behind the Attempt to Control Your Thoughts, Speech, and Life
Brownstone Institute | June 30, 2023
Keeping up with the corruption of the Covid regime feels like drinking from a firehose. The volume of the fraud, the pace of new discoveries, and the breadth of the operations are overwhelming. This makes it imperative for groups like Brownstone Institute to digest the onslaught of information and communicate salient themes and dispositive facts, particularly given the dereliction of mainstream media.
On Monday, the House Judiciary Committee released a report on how the Cybersecurity and Infrastructure Security Agency (CISA) “colluded with Big Tech and ‘disinformation’ partners to censor Americans,” adding to the informational firehose we work to imbibe.
The 36-page report raises three familiar issues: first, government actors worked with third parties to overturn the First Amendment; second, censors prioritized political narratives over truthfulness; and third, an unaccountable bureaucracy hijacked American society.
- CISA’s Collusion to Overturn the First Amendment
The House Report reveals that CISA, a branch of the Department of Homeland Security, worked with social media platforms to censor posts it considered dis-, mis-, or malinformation. Brian Scully, the head of CISA’s censorship team, conceded that this process, known as “switchboarding,” would “trigger content moderation.”
Additionally, CISA funded the nonprofit EI-ISAC in 2020 to bolster its censorship operations. EI-ISAC worked to report and track “misinformation across all channels and platforms.” In launching the nonprofit, the government boasted that it “leverage[d] DHS CISA’s relationship with social media organizations to ensure priority treatment of misinformation reports.”
The switchboard programs directly contradict sworn testimony from CISA Director Jen Easterly. “We don’t censor anything… we don’t flag anything to social media organizations at all,” Esterly told Congress in March. “We don’t do any censorship.” Her statement was more than a lie; it omitted the institutionalization of the practice she denied. The agency’s initiatives relied on a collusive apparatus of private-public partnerships designed to suppress unapproved information.
This should sound familiar.
Alex Berenson gained access to thousands of Twitter communications that uncovered concrete evidence that government actors – including White House Covid Advisor Andy Slavitt – worked to censor him for criticizing Biden’s Covid policies.
White House Director of Digital Strategy Rob Flaherty privately lobbied social media groups to remove a video of Tucker Carlson reporting the link between Johnson & Johnson’s vaccine and blood clots.
Facebook worked with the CDC to censor posts related to the Covid “lab-leak” hypothesis. Company employees later met with the Department of Health and Human Services to de-platform the “disinformation dozen,” a group including Robert F. Kennedy, Jr.
These were not cherry-picked examples – they were part of an institutional collusion to strip Americans of their First Amendment rights. Journalists Michael Shellenberger and Matt Taibbi exposed the “Censorship Industrial Complex,” a collection of the world’s most powerful government agencies, NGOs, and private corporations that worked together to silence dissent.
The Supreme Court has held that it is “axiomatic” that the government cannot “induce, encourage, or promote private persons to accomplish what it is constitutionally forbidden to accomplish.” Yet, CISA has joined the disturbing tendency of public-private partnerships designed to impede Americans’ right to information and freedom of speech.
- Political Operatives
Second, these programs were not idealistic attempts to promote the truth; they were calculated programs designed to quash inconvenient but truthful narratives.
The report outlines how CISA censored “malinformation – truthful information that, according to the government, may carry the potential to mislead.” Journalist Lee Fang later wrote that the malinformation campaign “highlights not only the broad authority that the federal government has to shape the political content available to the public, but also the toolkit that it relies upon to limit scrutiny in the regulation of speech.”
In this system, uncensored information has a tacit government approval, amounting to a system of widespread propaganda.
“State and local election officials used the CISA-funded EI-ISAC in an effort to silence criticism and political dissent,” the report notes. “For example, in August 2022, a Loudon County, Virginia, government official reported a Tweet featuring an unedited video of a county official ‘because it was posted as part of a larger campaign to discredit the word of’ that official. The Loudon County official’s remark that the account she flagged ‘is connected to Parents Against Critical Race Theory’ reveals that her ‘misinformation report’ was nothing more than a politically motivated censorship attempt.”
The officials supporting the operation remained unrepentant in their aim to advance political agendas. Dr. Kate Starbird, a member of CISA’s “Misinformation & Disinformation” subcommittee, lamented that many Americans seem to “accept malinformation as ‘speech’ and within democratic norms.”
Of course, the program explicitly violated the Constitution. The First Amendment does not discriminate based on the veracity of a statement. “Some false statements are inevitable if there is to be an open and vigorous expression of views in public and private conversation,” the Supreme Court’s controlling opinion held in United States v. Alvarez. But CISA – led by zealots like Dr. Starbird – appointed themselves the arbiters of truth and worked with the most powerful information companies in the world to purge dissent.
This was part of a larger political campaign.
Hunter Biden’s laptop, natural immunity, the lab-leak theory, and side effects of the vaccine were all censored at the government’s behest. The truth of the reports were not at issue; instead, they presented inconvenient narratives for Washington’s political class, who then used the Orwellian label of “malinformation” to lend cover to eviscerating the First Amendment.
- The Terror of the Administrative State
Third, the report exposes the increasing power of the administrative state. Federal bureaucrats rely on anonymity and unaccountability. Private industry employees could never oversee a disaster like the Covid response and maintain their jobs. It’d be like if BP’s head of safety for the Gulf of Mexico received a promotion after the oil spill.
But unelected officilals like CISA officials enjoy ever-increasing power over Americans’ lives without having to answer for their calamities. Suzanne Spaulding, a member of the Misinformation & Disinformation Subcommittee, warned that it was “only a matter of time before someone realizes we exist and starts asking about our work.”
Spaulding’s comment reflects the power that CISA wields and the benefit it derives from its lack of public exposure. Most Americans have never heard of CISA despite its overwhelming influence over lockdowns.
In March 2020, CISA divided the American workforce into categories of “essential” and “nonessential.” Within hours, California became the first state to issue a “stay at home” edict. This began a previously unimaginable assault on Americans’ civil liberties.
The House Report indicates that CISA was a central actor in censoring criticism of the Covid regime in the ensuing months and years. The agency is representative of the cabal of censorial and unaccountable officials engaged in public-private partnerships designed to keep us in the dark.
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The Crusades – colliding narratives
Ashes of Pompeii | June 13, 2026
They say history is written by the victors, but the Crusades offer an interesting historical contrast: a two-century collision that produced not one history, but two parallel, irreconcilable realities. The dates and the battles are identical in both accounts, but the moral axis is entirely flipped.
In the traditional Western narrative, the Crusades are framed as a heroic, if tragic, epic. The First Crusade is a pious pilgrimage; the knights are romanticized figures of chivalry in shining armor, bravely holding the line in a hostile, exotic land. The eventual loss of the Holy Land is mourned as the “fall of Outremer,” a tragic retreat of European civilization. In this telling, the East is often reduced to a passive backdrop, its inhabitants viewed through a lens of mystique or backwardness, mere obstacles to a divine mandate.
But cross the Mediterranean, and the exact same timeline reads like a chronicle of foreign invasion and eventual, hard-won restoration against the barbarous northerners. The dates do not change, but the adjectives do. Here is the history as it is remembered in the Levant… continue
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