How an illusion of efficacy can be established for any treatment
Norman Fenton | October 23, 2022
In determining the efficacy of a medical intervention (such as a drug or vaccine) to stop a particular disease or virus it is typical to assume that the treatment needs time to work before a person is classified as ‘treated’. For example, a person vaccinated against a virus may be classified as ‘unvaccinated’ until 2 weeks after getting the vaccination. This simple animation with a hypothetical example shows that, with such a classification, a placebo (i.e. no effect) vaccination can be shown to be highly effective.
See also this article for more context https://www.normanfenton.com/post/mor… and note that this applies to observational studies rather than randomized controlled trials
October 24, 2022 Posted by aletho | Deception, Science and Pseudo-Science, Timeless or most popular, Video | COVID-19 Vaccine | Leave a comment
This sick biotech craze must be halted before another disaster strikes
By Guy Hatchard | TCW Defending Freedom | October 21, 2022
RESEARCHERS at Boston University have developed a deadly new strain of Covid, which kills 80 per cent of animal subjects. The research was funded by the US government and approved by Anthony Fauci. I don’t need to tell you how risky such experiments are, or how stupid. This is just one biotechnology experiment among thousands currently being carried out around the world which pose similar kinds of threat. Each additional experiment adds to the danger and brings another lab escape a bit closer.
Biotechnology and medical science is already a long way down a well-worn path which leads to the normalisation of risk. This has involved gradual acclimatisation to high rates of severe injury and death imposed on an unwitting public. The psychology of this process is well known. Repeatedly turning a blind eye to suffering coarsens individual attitudes.
A past true-crime Forensic Files episode illustrates how far we have come. A young female doctor died unexpectedly of a heart attack. In those pre-pandemic times sudden death was a red flag necessitating the close attention of pathologists and police. In the episode, the presence of an unusual toxin was found and the culprit apprehended. By contrast, in the post-pandemic world sudden death has been normalised. No investigation required. Legislation is being changed to allow ‘cause unknown’ on death certificates.
High rates of excess all-cause death, pregnancy irregularities, cardiac events, cancers at lower ages and low birth rates have not just failed to raise eyebrows, but have been dismissed by ‘experts’ and MSM alike on flimsy pretexts without adequate investigation. Blaming Covid infection for every increase in illness has become the norm. This indicates detachment from sound science and the rational mind. Questions are off the table.
Last week New Zealand’s top vaccinologist Dr Helen Petousis-Harris sounded a public note of alarm, saying she wasn’t having any more boosters and advising the public to follow her example. Her advice was based on evolving scientific findings. This was a step too far for the MSM. The NZ Herald decided to switch experts, stoke the fear factor and cancel Dr Petousis-Harris.
The Herald quoted a University of Auckland computational biologist David Welch, who is not an expert on vaccines but begged to differ from Petousis-Harris saying: ‘I think we should be regularly having boosters. At the moment a booster twice a year looks like it would be very sensible because we’re getting waves more frequently than that.’ The long article failed to mention adverse effects of mRNA vaccination and its near-total lack of effectiveness.
Such buffoonery is not just uninformed, it increasingly appears to be part of a deliberate attempt to whitewash medical harm on a scale that dwarfs any previous example. An article in the Epoch Times headed ‘How Cancer Deaths From the COVID Jabs Are Being Hidden’ outlines just one way this is being accomplished, saying:
- Analysis of US Morbidity and Mortality Weekly Report (MMWR) data suggests that some cancer deaths have been redesignated as Covid deaths since April 2021. This has hidden the cancer signal.
- Before it was manipulated to eliminate the safety signal, data from the Defense Medical Epidemiology Database (DMED) showed cancer rates among military personnel and their families tripled after the rollout of the shots
- After the rollout of the Covid jabs in 2021, cancer patients have got younger, with the largest increase occurring among 30-to-50-year-olds. Tumour sizes are dramatically larger, multiple tumours in multiple organs are becoming more common, and recurrence and metastasis are increasing.
Why is this not front-page news? The controlling conservative elements of the medical profession and the profitable pharmaceutical industry consider vaccine adverse effects to be a sort of unspeakable heresy. Yet ask someone who has been working in the gene therapy field for years and a tsunami of cancers is not unexpected.
Look at it this way. Cancers result from mutated genetic instructions. These can result from a number of causes including oxidative stress, inherited weakness, environmental or ingested toxins. Inside every one of trillions of human cells every day microbiological immune processes make 70,000 DNA repairs. These ward off potential cancers.
These internal cellular immune processes are sealed off and protected behind the cell wall. The mRNA vaccines are Trojan horses designed to breach the cell wall and reprogram cellular activity. It doesn’t take a genius to appreciate that there are risks involved. These risks include cancers. Cancers normally take years to develop. The surge in cancers among US Department of Defense personnel should be a red flag. Instead medical administrators are apparently busy burying it.
In New Zealand the burying has involved withholding data from public scrutiny, making misleading comparisons, cancelling those asking questions, saturation government advertising promising safety, and indiscriminate use of the ‘conspiracy theory’ label. We have written about these for a year now. Given recent Covid scientific publishing, we are all hoping that the penny will drop. Perhaps those awake enough to study journal papers carefully will, like Dr Petousis-Harris, begin to realise that there is no point in endangering their own health for the sake of a biotechnology dream.
Even though we are approaching the end game of one mRNA biotech dream, there are thousands of others in the pipeline. The psychology of biotech dreaming allows proponents to segue effortlessly from one dream segment to another without a pause. As long as you believe in the ultimate good of human genetic manipulation, there is no real worry if a few people die along the way.
As things have progressed from a few dying, to thousands, to hundreds of thousands around the world and millions injured, coarsened attitudes have hardened. The progress of biotechnology has gradually come to be regarded by the medical elite and giant commercial interests as ‘a necessary task’. A task that requires toughness and determination to arrive eventually at a ‘laudable’ and inevitable goal. The echoes from history are obvious.
But what if the whole enterprise of biotechnology is misguided? Like the discovery of the atomic bomb, literally a dead end? Where the next available step is only a bigger bomb or a more invasive and deadly toxin or pathogen? There are good reasons to suppose this is the case. Millions of years of evolutionary interaction with the wider global epigenetic bionetwork, underpinned by the immutable laws of physics, just might be more reliable than the ideas of a mad scientist.
Is the complexity of human physiology beyond human comprehension and calculation? Yes. Our knowledge of it remains primitive. Moreover there are inherent limitations to our understanding. The full intricacies of in vivo genetic processes are not open to scrutiny. The computational solution of genetic processes and intercellular interactions is beyond the reach of even the most powerful supercomputers. Combinative processes between genes performing multiple tasks requires multidimensional mathematics involving unsolvable equations. Adverse effects of gene editing are known to be inevitable and incalculable.
Governments have poured billions of dollars into biotechnology training and research programmes. The false rationale for this has been created by vast public relations efforts funded by a great variety of global commercial interests. It has all the hallmarks of a Ponzi scheme or an unsustainable investment bubble. There are no beneficial or bankable outcomes appearing at the end of the pipeline. More alarmingly, the deficits in human health are taking their toll and making their presence felt.
Scientific American reported this week that ‘the U.S. Just Lost 26 Years’ Worth of Progress on Life Expectancy’. How low are our medical czars prepared to go before admitting that something is rotten in the state of Denmark? The ‘it’s not me’ and ‘look the other way’ cultures are in full flood to protect the mRNA PR mirage. Against all scientific logic and evidence, biotech CEOs, paid scientists and government experts, floundering politicians and funded media are still talking up the wondrously protective achievements of pandemic responses as if they have saved the public rather than endangered them, from the Wuhan lab to the Covid jab.
It is time to ask some serious questions. The truth is that we are not just in danger of losing progress on life expectancy, but also four centuries of progress with scientific method.
We can’t escape the fact that commercial biotechnology involves an incredibly risky and inherently mutagenic worldwide programme of experimentation. This requires a proportionate response with a global reach. For this reason and many others, this Sunday the Hatchard Report will be launching a Campaign for Global Legislation Outlawing Biotechnology Experimentation known as GLOBE. Watch this space for more details and visit my webinar with Voices For Freedom for the launch.
October 23, 2022 Posted by aletho | Science and Pseudo-Science, Timeless or most popular, War Crimes | COVID-19 Vaccine | Leave a comment
How Worried Should We Be About Boston University’s Gain-of-Function Covid Virus That Kills 80% of Mice?
BY DR RANDALL BOCK | THE DAILY SCEPTIC | OCTOBER 23, 2022
This week, Boston University found itself at the centre of scorn over claims its laboratories were engineering a “SARS-CoV-3” virus that would (hypothetically) put humanity one lab-leak away from a renewed Covid pandemic.
In the midst of worldwide relief over SARS-CoV-2’s eventual replacement by the mild, ‘common cold’ Omicron variant, BU’s scientists have created de novo an “Omicron S-bearing virus”, potentially marrying Omicron’s transmissibility with the Wuhan strain’s dangerous pathogenicity.
Boston University leadership should not be shocked by the widespread condemnation of this experiment. It has its own hubris to blame: steamrolling neighbourhood opposition to the urban placement of America’s National Emerging Infectious Diseases Laboratories (NEIDL), through which BU amasses lucrative research grants. As the philosopher Spider-Man has said, “with great power, there must also come great responsibility.”
In this case, BU exhibits power, but avoids responsibility. The National Institutes of Health (NIH) is examining whether these experiments should have triggered a federal review as ‘gain of function’ with SARS CoV-2’s gaining new or enhanced abilities, which NIH deems “inherently risky”. Boston University says it “did not have an obligation to disclose this research”, despite having received federal NIAID funding which BU states was only for “tools and platforms” used by the scientists.
“We take our safety and security of how we handle pathogens seriously, and the virus does not leave the laboratory,” noted NEIDL’s Dr. Ronald Corley. Cynics might point out that as recently as 2018, the Wuhan Institute of Virology (WIV) touted that its work “held the secret to preventing epidemics”. NEIDL has (probably) released fewer unintentional pandemics than WIV, so there’s that.
NEIDL can be seen as either a bulwark against – or conversely, a conduit for – bioterrorism. NEIDL houses the Level-3 Biosafety Lab (BSL-3) of this trans-viral graft experiment as well as one of the rare US BSL-4 laboratories, intended for studying the deadliest transmissible diseases, such as Ebola.
Lab-coat scientist researchers are not selected or rewarded for political acumen, nor should they be. Actual wet-lab work often embodies the phrase by which physicians tease anesthesiologists: “99% boredom and 1% panic” – but, without the panic. Instead, researchers have their 1%-portion comprised of the brief, refreshing glory on the occasion of publishing consequential results – the news of which usually stays within a small coterie of PhDs cognisant of the technical ‘twin-speak‘ pertinent to the narrow focus of the experiment performed.
Upending the news cycle, bringing fear and then furor to a Covid-weary populace, and a posse of paparazzi upon itself is not the usual modus operandi of researchers releasing a preprint dryly titled (as they often are): “Role of spike in the pathogenic and antigenic behavior of SARS-CoV-2 BA.12 Omicron“. Boston University’s Mohsan Saeed (et al.) ‘buried the lede‘ by not communicating clearly having formed a SARS-CoV-2 mutant through chimeric graft of Omicron spike onto SARS CoV-2.
The researchers’ insularity is evident in their not predicting that producing novel camouflage for the pandemic’s perpetrator would be sufficient cause for all hell to break loose. Given Dr. Saeed’s interim disappearance from the scene, it is assumed notoriety was not the researchers’ actual intent. His additional lack of communicating the societal need for a rejiggering of COVID-19 spare parts into a new mutant strain is its own problem.
NIAID says that the BU should have communicated in advance the purpose and nature of the study. BU responds that it did not have to because the primary funds were from BU itself. Medical ethicist Dr. Arthur Caplan says, “the entire research community would benefit from better communication.” Perhaps even earlier “better communication” might have obviated the experiment itself.
By focusing so intently within the micro-world, it’s perhaps forgivable virologists lose sense of the macro. Conversely, the general public has earned every right to be twitchy and tetchy over ‘gain of function’ engineered augmentations to SARS-CoV-2 after the many millions of excess deaths following what many suspect was a Wuhan lab leak.
The Daily Mail’s story headlined “‘This is playing with fire – it could spark a lab-generated pandemic’” had this graphic stating the mutant strain has an 80% kill rate.

Sensationalism definitionally entails shocking language at the expense of accuracy. Corrections are therefore in order:
- Yes, this lab is performing a ‘Frankenstein’s monster’ experiment: putting Omicron’s spike protein (head) on ancestral SARS CoV-2’s envelope (body) – but, this is the standard operating procedure for virologists. Chimeric work allows comparisons to be made gauging the relative strength or pathogenicity of individual virion segments.
- Yes, this is a brand-new ‘deadly strain’ – but for a particularly and purposefully vulnerable strain of mice, not for humans. The new ‘Frankenstein’ Omicron-spike-and-Wuhan-body chimeric coronavirus caused 80% of hACE-2 lab mice to die – fewer, actually, than had perished from the ancestral Wuhan SARS-CoV-2 itself. For better or worse, these mice have been specifically genetically engineered to have 100% fatality to SARS-CoV-2. If the mice instead replicated human’s very low fatality rate against this virus (less than 0.1% in the non-vulnerable), it would be nigh impossible to make any statistically significant judgements in any experiment unless multi-thousands of mice were included in every phase.
This specific type of work was performed in an appropriate BSL-3 laboratory, and was technically legal even though it encompassed ‘gain of function‘ work. There had been a moratorium in the mid-2010s on such potentially dangerous work within the United States, but that was repealed in 2017. The rationale for reversing the moratorium was similar to that of any military’s maintaining and testing weaponry and engaging in wargames: “Researchers deliberately make viruses more dangerous to help prepare better responses to outbreaks that might occur naturally.”
Ostensibly, the moratorium was lifted to keep us safe; however, it was instituted for the very same reason, in 2014, to curtail scientists’ juicing up avian flu.
In 2011, Fouchier and Kawaoka alarmed the world by revealing they had modified the deadly avian H5N1 influenza virus so that it spread between ferrets (animals used for their similarity to humans’ influenza response). Critics worried a souped-up virus could spark a pandemic if it escaped from a lab (accidentally or as bioterror).
The flip-flopping in allowing gain of function research points to the dual needs in relation to such cutting edge science. Even as the moratorium was lifted, there were rules about the flow of information on gain of function experiments. Open communication is a prerequisite to scientific innovation but also can provide ready blueprints for any intrepid bioterrorist. An additional complication is that almost every study in the U.S. receives federal funds, creating a loophole of having to divulge sensitive results through any given FOIA request.
It is uncertain if BU’s newly chimeric COVID-19 mutant could qualify as a bio threat. Personally, I think not. Almost every one of its mutations is less efficacious than the parent. Viruses go through trillions in order to adapt sequentially to changing immune systems amongst the host. That researchers would come up with a highly dangerous one on the first try seems unlikely. In any event, there is vast natural immunity to Omicron and natural and vaccine immunity to ancestral SARS-CoV-2, COVID-19.
So what was the purpose of the BU NEIDL team? Since poor communication seems to be a threat throughout this story, it is perhaps no surprise that this preprint’s abstract section lacks clarity – and features instances of ‘begging the question (highlighted).
The recently identified, globally predominant SARS-CoV-2 Omicron variant (BA.1) is highly transmissible, even in fully vaccinated individuals, and causes attenuated disease compared with other major viral variants recognised to date. The Omicron spike (S) protein, with an unusually large number of mutations, is considered the major driver of these phenotypes. We generated chimeric recombinant SARS-CoV-2 encoding the S gene of Omicron in the backbone of an ancestral SARS-CoV-2 isolate and compared this virus with the naturally circulating Omicron variant. The Omicron S-bearing virus robustly escapes vaccine-induced humoral immunity, mainly due to mutations in the receptor binding motif (RBM), yet unlike naturally occurring Omicron, efficiently replicates in cell lines and primary-like distal lung cells. In K18-hACE2 mice, while Omicron causes mild, non-fatal infection, the Omicron S-carrying virus inflicts severe disease with a mortality rate of 80%. This indicates that while the vaccine escape of Omicron is defined by mutations in S, major determinants of viral pathogenicity reside outside of S.
Let’s translate the abstract into general English:
Omicron is milder – and its spike protein is structurally different enough from the ancestral Wuhan strains that an mRNA vaccine to SARS CoV-2 does nothing to protect mice from Omicron. This is somewhat immaterial because Omicron doesn’t make these mice sick in the first place (basically the same situation as with humans). So, with research funding in hand, what are we going to do? Let’s put an Omicron ‘Halloween mask’ on the dangerous Wuhan strain! How many mice will die? A lot, nearly 80%. That’s sounds really bad, but we forgot to mention (in this abstract) that Wuhan strain without the Omicron-spike mask kills 100% of these mice, which sadly are canaries in a coal mine, engineered to die from SARS-CoV-2. Conclusion: the stuff inside the SARS-CoV-2 envelope is the really bad stuff. With its very own original spike protein it’s more dangerous, but what did we expect? We just made a virus that’s different from a fairly dangerous one and it’s not quite as dangerous.
Thus restated, it becomes difficult to ascertain the genuine need for doing this experiment (whose results seem obvious, predictable and axiomatic). Einstein favored Gedankenexperimente (‘thought experiments’) using conceptual rather than actual experiments in creating the theory of relativity. There’s nothing like the ‘real thing’, but I’m imagining 99% of virologists could have foreseen a conclusion similar to this without having done any of the study. Moreover, most would not have seen a real point in doing this study in the first place. Of course, getting paid and churning research grants can help provide motivation.
Even without the researchers’ having read my own article “Is it Time to Accept That Omicron is not COVID-19?” in The Daily Sceptic, September 25, 2022 – they should still have had enough information to know Omicron (despite its Greek letter) is not a SARS CoV-2 variant nor lineal genomic or genetic descendent. Such information was easily available January 2022. With this in mind, the highlighted portions make little sense and the purpose of the study even less.
One virologist offered these criticisms of the preprint’s study (in confidence):
- Why put Omicron S on a virus that is no longer circulating? I’m not sure what scientific question they are trying to answer.
- The grants that are cited for the work were meant to study innate immunity. They claim they want to study the role of spike protein in phenotype but they are not using the proper controls.
- It would have made more sense to have reversed the experiment, i.e., put the Wuhan spike on the Omicron envelope.
- Also, site-directed mutagenesis (creating specific, targeted changes) would have been a more useful technique, given that there are so many mutations in Omicron’s spike protein compared to earlier variants.
- The authors’ conclusion, “These findings indicate that the S protein is not the primary determinant of Omicron’s pathogenicity in K18-hACE2 mice,” should say that “S protein was not a primary determinant of Wuhan pathogenicity”.
- They actually [downwardly] attenuate the Wuhan strain by putting the Omicron-S onto that virus, yet try to sell it as if they had made the virus more lethal.
- Overall, they seem to really be studying Wuhan pathogenicity in the context of Omicron spike.
All products and methods of technology (e.g. nuclear power, mining, fossil fuels) are variously considered ‘double-edged swords’. So too it is with these studies. There are potential benefits and potential risks. In this particular case, were the risks worth it? Was the study appropriately directed and was the information gleaned worth the global consternation? The answer to both is ‘no’.
“It’s not like they made this monster virus, that’s a complete misinterpretation,” states infectious disease specialist Dr. Daniel Kuritzkes. “Researchers compared the ancestral version, Omicron, and a combined version of the two to research what piece of the virus dictates how sick a person will get. What we see in animal models does not translate directly to what we will see in humans. The labs are extraordinarily careful in how they do these experiments. There are strict protocols in place to make sure that nothing produced in the lab is released into the environment.”
My assessment is that this is more ‘tempest in a teapot’ than monster – although Dr. Frankenstein’s methods and ethical issues find resonance here. That there is a federal investigation into this case is interesting for the side reason that it seems an admission against its own interest, namely to the possibility that virology laboratories can potentially leak mutant strains. Who would’ve thought? For so long, it was all but forbidden to consider such a possibility for China’s WIV, even though ancillary evidence is nearly conclusive it occurred.
Dr. Randall Bock is a primary care physician near Boston, Massachusetts, and the author of Overturning Zika.
October 23, 2022 Posted by aletho | Science and Pseudo-Science, Timeless or most popular | Covid-19, United States | Leave a comment
Who Blew Up Nord Stream Pipelines? | A Mystery!
Matt Orfalea | October 23, 2022
October 23, 2022 Posted by aletho | Deception, False Flag Terrorism, Timeless or most popular, Video, War Crimes | Germany, United States | Leave a comment
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 aletho | Corruption, Deception, Science and Pseudo-Science, Timeless or most popular | COVID-19 Vaccine, United States | Leave a comment
New Study Blames COVID on NIH, University of North Carolina — Finds Fauci and Baric’s Fingerprints on Pandemic Bug

By Robert F. Kennedy, Jr., J. Jay Couey, Ph.D., and Charles Rixey | The Defender | October 21, 2022
Critics have long questioned why the National Institutes of Health (NIH) would fund experiments by University of North Carolina of Chapel Hill (UNC) professor Ralph Baric to develop a technique for hiding evidence of human tampering in laboratory-created super viruses.
Aided by some $220.5 million in National Institute of Allergy and Infectious Diseases (NIAID) funding, Baric developed a so-called “Seamless Ligation” technique, which he boasted could perfectly conceal all evidence of human tampering in laboratory-created viruses. Baric nicknamed his invention the “no-see’m” method.
Now a new study, “Endonuclease fingerprint indicates a synthetic origin of SARS-CoV2,” published on the preprint server bioRxiv, shows that — apparently unbeknownst to Baric — the “seamless ligation” concealment gimmick leaves its own minute but legible signature.
Most momentously, these same researchers have discovered that damning signature in the genome of the virus that causes COVID-19.
Baric’s technique has long been controversial. “It’s the artist that doesn’t sign his name to the painting; the virologist that doesn’t put his signature into the virus to let us know whether or not it is emerging naturally or whether it is produced in a laboratory,” said Jeffrey Sachs, chair of The Lancet COVID-19 Commission, a task force that investigated the origins of COVID-19.
“All of it says, my God, there was really a big, very risky research agenda underway.”
This month, Sachs published the results of his 22-month investigation in The Lancet, including the damaging conclusion that COVID-19 was probably laboratory-generated and that the technology probably came from NIH-funded science.
Referring to Baric’s seamless ligation methodology, evolutionary biologist Bret Weinstein observed:
“It’s the exact opposite of what you would do if your interest was public health. Public health scientists would be marking their enhancements with red flags — not devising ways to hide them. The only reason you would want a concealer is to advance a sinister purpose — such as illegal bioweapons development — some mischief that the scientist didn’t want traceable back to his lab.”
Baric taught his “no-see’m” method to the Wuhan Institute of Virology’s (WIV) “Bat Lady” Shi Zhengli in 2016. In return, Baric received Chinese coronaviruses collected by Shi from bats in Yunnan province. (Scientists have linked the COVID-19 genome’s pedigree to closely related bats.)
Shi and her colleagues at the Wuhan Institute subsequently demonstrated their mastery of Baric’s high-risk technique in a series of published — and highly controversial — gain-of-function experiments at the Wuhan lab. It has been even more puzzling to his critics that Baric, again with NIAID funding, chose to share this dangerous technique for weaponizing pathogens with Chinese scientists who have clear links to the Chinese military.
Experts say that the implications of this new study could be far-reaching. By pointing the finger at Baric, the study raises the possibility of potentially devastating liability for the NIAID and the University of North Carolina and other parties.
Scientists, including those close to Dr. Anthony Fauci, have repeatedly pointed out that SARS-CoV-2, the virus that causes COVID-19, has genomic sequences that appear inconsistent with natural evolution: The COVID-19 virus is no longer infectious in bats, and its spiked protein feature — which is unknown in this family of coronavirus — includes numerous mutations that make it ideally infectious in humans.
The closest known coronavirus relative — a coronavirus from the Wuhan lab — is 96.2% identical to SARS-CoV-2. The peculiar spike accounts almost completely for the entire 3.8% difference. Oddly, there are multiple novel mutations in the spike and almost none in the rest of the genome.
Natural evolution would be expected to leave mutations distributed evenly across the genome. The fact that virtually all the mutations occur on the spike led these scientists to suspect that that particular Wuhan lab coronavirus collected by Shi Zhengli is the direct progenitor of SARS-CoV-2 and that its new spike was implanted through engineering.
However, the unmistakable fingerprints of lab engineering were absent — leaving many experts wondering whether Baric’s technique was used to assemble a novel coronavirus with the engineered spike while removing the evidence of lab generation.
This new study connects the biological breadcrumbs that link federally funded research to a global pandemic. That trail leads directly to UNC and NIAID.
The authors of the study — a team of researchers from Duke University, University Clinics of Würzburg and an industry group — identified a characteristic signature in the amino acid code. That indelible artifact could only have emerged from Baric’s “no-see’m” methodology.
In an interview last spring, Baric himself confessed, that at the time the pandemic began, only two or three labs in the world were using his protocol – including his UNC lab and the WIV.
The study’s authors’ conclusions rest on the presence of unique sites in the COVID-19 virus. These sites allow special enzymes called “restriction enzymes” to cut the DNA into building blocks of unique size that then can be “stitched together in the correct order of the viral genome,” according to the study’s authors.
Essentially, Baric’s technique leaves behind unique spellings in the “genetic vocabulary.” The new words include “odd spelling choices” subtly distinguishing them from typical viral vocabulary.
The magic of Baric’s “no-see’m” technique is to invisibly weave these telltale “spelling” changes into the viral sequence between relevant genes without altering the viral protein. This is like changing the “spelling” of the word without changing its meaning; the casual listener will never notice the difference.
The research team used forensic tools to drill down on minute “spelling differences” in the SARS-CoV2 genome that betray laboratory tampering using the “no-see’m” technique.
Consider how a Brit would spell “colour,” “manoeuvre” or “paediatric.” The choice to spell a word in a certain way can reveal your nation of origin. Similarly, these nearly imperceptible changes in the viral sequence give away the laboratory origins of this virus.
In sharing his seamless ligation technique with Shi Zhengli, Baric assured that the WIV possessed all the required elements of the assembly process. EcoHealth Alliance’s infamous DEFUSE proposal describes the same techniques in detail. (submitted to The Defense Advanced Research Projects Agency, or DARPA, in 2018).
The world now has proof positive that SARS-CoV2 is an engineered laboratory creation generated with technology developed by Ralph Baric with U.S. government funding.
Prosecutors and private attorneys representing clients injured by the COVID-19 pandemic now have a smoking gun. The gun points at humanity. Forensic scientists have now successfully lifted faint but precise fingerprints from the lethal pistol’s grip and trigger. Those fingerprints belong to the NIAID and the University of North Carolina.
Baric is Fauci’s favorite gain-of-function scientist. The cascade of NIAID funding to Baric and his UNC lab has financed 152 studies approaching a quarter-billion dollars.
Those federal grants have made Baric the global kingpin of gain-of-function science. In conformance with standard practice, it is probable that UNC pockets one-quarter to one-half of NIH’s financial felicities to Baric for “administrative costs.”
These monumental payments have probably incentivized UNC to turn a blind eye to Baric’s reckless experiments and to his controversial decision to transfer his dangerous technologies to a Chinese military laboratory known to suffer from deficient safety protocols and shoddy construction that make it, in the words of Congressional investigators, less secure than a “dentist’s office.”
UNC’s role in enabling the questionable conduct may have precipitated a global pandemic that could easily give rise to liability for negligence.
UNC and NIAID’s liability is now clear. But do we have positive proof that the Wuhan lab created the monstrosity that caused COVID-19?
The cumulative evidence strongly suggests that the Wuhan lab used Baric’s methodologies to cobble together the chimeric virus that caused the COVID-19 pandemic. But a few missing puzzle pieces still prevent us from definitively proving that this dangerous construction project occurred at the Wuhan lab.
As The Lancet Commission report concluded, the released emails show that NIH’s Dr. Francis Collins, NIAID’s Fauci and EcoHealth Alliance’s Peter Daszak, and others are continuing to collaborate with Shi Zhengli and Chinese officials to suppress the public release of information that would allow us to complete this picture. Stay tuned!
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 22, 2022 Posted by aletho | Timeless or most popular, War Crimes | Anthony Fauci, Covid-19, NIAID, NIH, Ralph Baric, United States, University of North Carolina | Leave a comment
10 MINUTES COVID MADNESS. #NEVERFORGET
Credit: Professor Freedom
October 22, 2022 Posted by aletho | Science and Pseudo-Science, Timeless or most popular, Video | Covid-19 | 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 aletho | Science and Pseudo-Science, Timeless or most popular | COVID-19 Vaccine | 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 databasesThe 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 aletho | Corruption, Deception, Science and Pseudo-Science, Timeless or most popular | COVID-19 Vaccine, UK | Leave a comment
‘Insane’: Boston Researchers Create ‘More Lethal’ Strain of COVID, Prompting Calls to Shut Down Risky Gain-of-Function Research
By Michael Nevradakis, Ph.D. | The Defender | October 18, 2022
A team of 14 scientists at Boston University’s National Emerging Infectious Diseases Laboratories (NEIDL) developed a new strain of COVID-19 that killed 80% of the mice infected with the virus in a laboratory setting, according to a preprint study published Oct. 14.
Following the announcement, numerous news stories about the study’s results focused on the fatality rate observed in the laboratory mice used in the study.
However, behind the headlines, some scientists and others raised concerns about the nature of the research and the fact that it was partially funded by the National Institute of Allergy and Infectious Diseases (NIAID), headed by Dr. Anthony Fauci.
The research was conducted using what some scientists called “gain-of-function” research, raising concerns that this type of research — which some theorize led to the creation and escape of the original Wuhan strain of COVID-19 — is still being done, despite concerns that it could lead to more lab escapes and more pandemics.
Gain of function refers to the “manipulation of pathogens to make them more dangerous,” in the hope of “getting ahead of a future outbreak.”
Commenting on the researchers’ announcement, Robert F. Kennedy, Jr., Children’s Health Defense chairman of the board and chief legal counsel, remarked on the potential danger of such research — and its federal funding:
“What could be more insane than Anthony Fauci funding more of his GOF [gain of function] experiments to soup up coronavirus lethality in the middle of a pandemic caused by a juiced-up coronavirus that has killed millions?
“All of horrified humanity is watching Lord Of The Flies play out at NIH [National Institutes of Health] and praying for the adults to appear.”
Rachel Lapal Cavallario, Boston University’s associate vice president for public relations and social media, told the media the research conducted was not gain-of-function research and that, “In fact, this research made the virus [replication] less dangerous.”
However, others disputed that claim.
Sen. Roger Marshall (R-Kan.), a doctor, said the research involved “lethal gain of function virus research” that creates the “potential to kill more people than any singular nuclear weapon.”
“Viruses have managed to escape even the most secure labs,” Marshall said, adding that this type of “research must stop immediately while the risks and benefits can be investigated.”
Jessica Rose, Ph.D., commenting on the NEIDL research on Substack, wrote:
“What they have done in this work, as described by their own methods and results, is akin to madness.
“It is akin to madness because … they basically created and published a recipe for a deadly pathogen (80% mortality rate in the subjects of their experiments) of their own construction in their lab.
“By the way, this is precisely gain-of-function research. It couldn’t be more descriptive.”
Boston University today issued the following statement, downplaying the risks of the research:
“The research was reviewed and approved by the Institutional Biosafety Committee (IBC), which consists of scientists as well as local community members. The Boston Public Health Commission also approved the research.
“Furthermore, this research mirrors and reinforces the findings of other, similar research performed by other organizations, including the FDA. Ultimately, this research will provide a public benefit by leading to better, targeted therapeutic interventions to help fight against future pandemics.”
Efforts to prevent construction of NEIDL BSL-4 lab failed
NEIDL describes itself as “a Boston University Center dedicated to research on emerging and re-emerging infectious diseases and the pathogens that cause them,” and “a major step forward in advancing public health” that “provide[s] the necessary information and understanding to develop diagnostic tests, treatments, and vaccines.”
NEIDL also claims that it “will not conduct any secret or classified research” and that “the public will have access through several channels to information about any and all research before it even begins” — making NIAID’s claims that it was unaware of the spike protein research project all the more perplexing.
According to the Daily Mail, NEIDL is one of 13 biosafety level 4 (BSL-4) labs in the U.S.
However, this particular research took place under BSL-3 precautions, although according to STAT, “There is no evidence the work … was conducted improperly or unsafely,” noting that an internal biosafety review committee and the Boston Public Health Commission approved the work.
The journal Nature described the difference between BSL-3 and BSL-4 as follows:
“BSL-3 laboratories are designed so that scientists can safely work with potentially lethal and inhalable pathogens in a contained environment. Experiments are conducted in sealed workspaces in which the air is filtered and not recirculated, and the entrance to the facility is typically secured by self-closing doors.
“BSL-4 facilities, in which researchers work with fatal pathogens that can spread through aerosols, and for which vaccines or treatments are lacking or limited, require extra security measures.”
University of Illinois international law professor Francis Boyle, J.D., Ph.D., said the dangers of BSL-4 facilities have long been known, which is why he participated in efforts to stop the construction of the NEIDL facility.
Boyle, a bioweapons expert who drafted the Biological Weapons Anti-Terrorism Act of 1989, told The Defender:
“Years ago, there was a lawsuit to prevent and stop the building of this BSL-4 [facility] at Boston University that I did work on, and we failed.
“At that time we argued that the BSL-4 would engage in existentially type dangerous biological warfare research, and that was even before … gain-of-function.
So, we knew from the get-go how dangerous this lab was going to be and tried to stop it. We tried, we failed, and now this Nazi biowarfare death science dirty work is going on.”
However, the Boston University facility was completed with $128 million in NIH funding.
Commenting on gain-of-function research in general, Boyle said:
“You’ll note it was funded by NIH and NIAID under Tony Fauci.
“The New York Times has pointed out that about 94% of all this Nazi biowarfare death science dirty work has been funded by NIH and NIAID since Reagan put him in charge of NIAID.”
According to Boyle, this has resulted in more than $100 billion in federal bioweapons spending since Sept. 11, 2001.
Boyle said the federal government “doesn’t rein in or prosecute” scientists working on such projects, “because the federal government is paying for this type of Nazi biowarfare death science dirty work.”
Such research, and the facilities in which it is performed, also pose a risk to surrounding communities and the world at large, Boyle said, suggesting a Wuhan-like leak could occur at any similar facility in the U.S.:
“This is another catastrophe waiting to happen, and that Boston University BSL-4 [facility] should be shut down immediately.
“They know full well how existentially dangerous this is, certainly for the metropolitan Boston area … and especially for the African American community in Dorchester surrounding that Boston University BSL-4 lab.”
For Boyle, “It’s not enough to ban gain-of-function.” He also called for BSL-3 and BSL-4 facilities, including the Boston University facility, a CDC facility in Atlanta and a new facility in Kansas where the federal Plum Island Animal Disease Center is being relocated, to be shut down.
“The only remedy here is to shut down all BSL-3s and BSL4-s in the U.S.A., immediately and effectively,” Boyle said. “Otherwise, there is going to be another leak.”
Notably, the Wuhan Institute of Virology where research involving “engineered novel bat coronaviruses” took place is said to have been performed in BSL-2 and BSL-3 facilities.
Rose questioned the lower safety conditions under which the NEIDL researchers created the hybrid strain, while also raising broader security concerns and calling for gain-of-function work to be “banned” and its products “destroyed immediately.”
She said:
“This paper reveals more than the successful creation of a deadly new virus. It [gives] this recipe in the methods to anyone with a decent lab to recreate it.
“They don’t even mention what the hell they are planning to do with this new virus! They don’t say a bloody word about the fact that they created a virus that for all intents and purposes, is a Level IV pathogen, so why the hell are they playing with it in a Level III [laboratory]?”
NIH claims it didn’t know what it was funding
According to NEIDL, grants from the NIH “provide the support for research at NEIDL.”
In September, the study’s lead author, Mohsan Saeed, Ph.D., received a five-year, $2 million grant from the NIAID, and a separate five-year, $2 million grant from the National Institute of General Medical Sciences, to “explore novel aspects of clinically important viruses and human defense mechanisms.”
Nancy J. Sullivan, NEIDL’s new director previously was chief of the Biodefense Research Section at NIAID’s Vaccine Research Center.
Following the publication of the preprint study — and the controversy that ensued — the NIAID appeared to distance itself from the research. According to STAT, “The research team did not clear the work” with the NIAID, leading the agency to look “for some answers as to why it first learned of the work through media reports.”
Dr. Emily Erbelding, M.P.H., director of the NIAID’s Division of Microbiology and Infectious Diseases, told STAT that the research team’s “original grant applications did not specify that the scientists wanted to do this precise work. Nor did the group make clear that it was doing experiments that might involve enhancing a pathogen of pandemic potential in the progress reports it provided to NIAID.”
Erbelding said the NIAID is “going to have conversations” with the research team in the coming days, adding that “we wish that they would have” informed NIAID of the “intent of the research.”
According to Erbelding, this would have likely resulted in a committee being convened “that would assess the risks and benefits” of the research involving “enhanced pathogens of pandemic potential.”
What the NEIDL researchers did
According to STAT, the NEIDL researchers set out “to determine if the mutations in the Omicron spike protein were responsible for this variant’s increased ability to evade the immunity to SARS-2 that humans have built up, and whether the changes led to Omicron’s lower rate of severity.”
The research involved extracting the Omicron variant’s spike protein and attaching it to the original strain.
Put differently, the scientists took the deadliest COVID-19 strain and combined it with the spike protein from the most infectious strain. They then infected laboratory mice and human cells with the new hybrid strain.
The results showed that while the Omicron variant’s spike protein was responsible for the variant’s ability to evade immunity developed via infection, vaccination or both, it is not responsible for the decrease in the severity of the Omicron strain.
According to the Daily Mail :
“The researchers looked at how mice fared against the new hybrid strain compared to the original Omicron variant.
“When a similar group of rodents were exposed to the standard Omicron strain, however, they all survived and only experienced ‘mild’ symptoms. …
“[The researchers] found the hybrid strain produced five times more viral particles than the original Omicron.”
According to the MetroUK, “The scientists also infected human cells with the hybrid variant and found it was five times more infectious than Omicron.”
In the preprint, the researchers wrote:
“We generated chimeric recombinant SARS-CoV-2 encoding the S gene of Omicron in the backbone of an ancestral SARS-CoV-2 isolate and compared this virus with the naturally circulating Omicron variant.
“The Omicron S-bearing virus robustly escapes vaccine-induced humoral immunity, mainly due to mutations in the receptor-binding motif (RBM), yet unlike naturally occurring Omicron, efficiently replicates in cell lines and primary-like distal lung cells.
“In K18-hACE2 mice, while Omicron causes mild, non-fatal infection, the Omicron S-carrying virus inflicts severe disease with a mortality rate of 80%. This indicates that while the vaccine escape of Omicron is defined by mutations in S, major determinants of viral pathogenicity reside outside of S.”
In a statement remarking on the outcome of the study, NEIDL’s Saeed, who is also an assistant professor of biochemistry at Boston University, said:
“Consistent with studies published by others, this work shows that it is not the spike protein that drives Omicron pathogenicity, but instead other viral proteins.
“Determination of those proteins will lead to better diagnostics and disease management strategies.”
Media focuses on study’s findings, but critics more concerned about the research itself
Some media outlets focused on the researchers’ findings that 100% of the mice infected with the engineered virus died.
Others, however, downplayed the study’s findings. According to Fox News, for example, one of the study’s limitations was that the specific breed of mice used may not provide an accurate model for the risk posed to humans, “as other types [of mice] are more similar to humans.”
In a blog post, commentator Alex Berenson, a former writer for The New York Times, also addressed the sensationalism surrounding the study’s findings, pointing out that while an 80% fatality rate in lab mice sounds bad, 100% of the mice that previously were infected with the wild variety of COVID-19 had died.
He wrote:
“[The research] says the Omicron/wild-type Sars-Cov-2 combination the researchers created is more lethal than Omicron.
“However, it ALSO says the Omicron/wild type virus is LESS lethal than [the] original wild type. Neither of those findings should be a surprise. Omicron is much less dangerous than the original Sars-Cov-2, so blending the two together produces a virus with intermediate lethality.
“What’s with the 80 percent mortality rate then? It’s in mice, people. And guess what? The wild-type had a 100 percent mortality rate in mice. Yes, all the mice infected with the original Sars-Cov-2 died. I think we can agree that Sars-Cov-2 does not have a 100 percent mortality rate in humans.”
Specifically addressing the probable risk to humans, Berenson added:
“Nor did the researchers provide any evidence that the blended Omicron/wild-type coronavirus is able to defeat antibodies in people who have been infected with and recovered from Omicron. Which is basically all of us. (They did show that both the original Omicron and their variant beats the mRNA vaccines, but that fact is not a surprise either.)”
Erbelding shared similar remarks, stating, “That 80% kill rate, that headline doesn’t tell the whole story, because Wuhan” — the original strain — “killed all the mice.”
In turn, behind its headline, the Daily Mail wrote, “The scientists admit the hybrid virus is unlikely to be as deadly in humans as it was in mice,” adding, “This is because the specific breed of lab mice used are very susceptible to severe COVID disease. Mice and humans also have very different immune responses to the virus.”
STAT also remarked on this point, writing:
“The fatality rate seen in this strain of mice when they were infected with these viruses raises questions about how good a model they are for what happens when people are infected with SARS-2. The Wuhan strain killed less than 1% of people who were infected.”
But Boyle and Rose and others, like David Livermore, Ph.D., a professor of microbiology at the University of East Anglia, and Shmuel Shapira, an Israeli government scientist, said the news coming out of NEIDL was less about the study’s results and more about the research itself.
Livermore told the Daily Mail, “Given the strong likelihood that the COVID pandemic originated from the escape of a lab-manipulated coronavirus in Wuhan, these experiments seem profoundly unwise.”
Shapira also condemned the research. “This should be totally forbidden, it’s playing with fire,” he said.
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 19, 2022 Posted by aletho | Science and Pseudo-Science, Timeless or most popular, War Crimes | Anthony Fauci, United States | Leave a comment
Arrests made in Dutch journalists case
El Salvador Perspectives | October 18, 2022
Forty years have past since their crimes were committed. But in the past week, former military figures from El Salvador’s civil war have been arrested for their roles in the cold-blooded killing of four Dutch journalists covering that war.
In early 1982, El Salvador was a dangerous place for journalists covering the civil war between FMLN guerrillas and the country’s armed forces. Despite the danger, Dutch journalists, Koos Koster, Jan Kuiper, Joop Willemse and Hans ter Laag, ventured out to the Department of Chalatenango to get an interview with guerrilla fighters. The Salvadoran army ambushed their group and killed all the journalists.
The ambush was one of the war crimes documented in the 1993 UN Truth Commission Report following the conclusion of El Salvador’s civil war:
On the afternoon of 17 March 1982, four Dutch journalists accompanied by five or six members of FMLN, some of them armed, were ambushed by a patrol of the Atonal Battalion of the Salvadorian armed forces while on their way to territory under FMLN control. The incident occurred not far from the San Salvador-Chalatenango road, near the turn off to Santa Rita. The four journalists were killed in the ambush and only one member of FMLN survived. Having analysed the evidence available, the Commission on the Truth has reached the conclusion that the ambush was set up deliberately to surprise and kill the journalists and their escort; that the decision to ambush them was taken by Colonel Mario A. Reyes Mena, Commander of the Fourth Infantry Brigade, with the knowledge of other officers; that no major skirmish preceded or coincided with the shoot-out in which the journalists were killed; and, lastly, that the officer named above and other soldiers concealed the truth and obstructed the judicial investigation…
1. The Commission on the Truth considers that there is full evidence that Dutch journalists Koos Jacobus Andries Koster, Jan Cornelius Kuiper Joop, Hans Lodewijk ter Laag and Johannes Jan Willemsen were killed on 17 March 1982 in an ambush which was planned in advance by the Commander of the Fourth Infantry Brigade, Colonel Mario A. Reyes Mena, with the knowledge of other officers at the El Paraíso barracks, on the basis of intelligence data alerting them to the journalists’ presence, and was carried out by a patrol of soldiers from the Atonal BIRI, under the command of Sergeant Mario Canizales Espinoza.
2. These same officers, the sergeant and others subsequently covered up the truth and obstructed the investigations carried out by the judiciary and other competent authorities.
During the war a judicial investigation of the events came to an end in 1988 when the judge on the case sought asylum outside of El Salvador after receiving death threats, and the 1993 amnesty law prevented any prosecution thereafter.
After the amnesty law was nullified, the Fundación Comunicándonos and the Asociación Salvadoreña para los Derechos Humanos (ASDEHU) filed a complaint on March 13, 2018 asking for El Salvador’s attorney general (FGR) to reopen the case and prosecute the military officers in command of the ambush. The ambassador to El Salvador from the Netherlands joined the human rights attorneys as they presented the demand, and expressed his hope that the FGR would investigate and bring the guilty to justice.
The case was reopened, and now arrest warrants have been issued by the judge.
El Faro English describes the week’s developments:
General Guillermo García, the minister of defense and strongman of the Salvadoran Army in the early 1980s, has been detained for his alleged responsibility in the murder of four Dutch journalists in 1982, members of the judicial branch involved in the case and two relatives of the victims confirmed to El Faro. Also arrested was Colonel Francisco Antonio Morán, the former director of the defunct Treasury Police, a fearsome security force tied to massacres, enforced disappearances, torture, and extrajudicial activities attributed to death squads.
The arrests were ordered on October 13 by Judge María Mercedes Argüello of the trial court in Dulce Nombre de María, Chalatenango, after finding sufficient grounds for the accused officers to face trial for the murder of Jacobus Andries Koster, Jan Cornelius Kuiper, Hans Ter Laag, and Johannes Jan Willemsen, Dutch journalists ambushed and executed by the Salvadoran Army on Mar. 17, 1982, in rural Chalatenango.
General García and Colonel Morán were detained in the early hours of Friday, October 14, in their homes in San Salvador. Their first hearing was set for Monday, October 17.
The court also ordered the arrests of Colonel Mario Adalberto Reyes Mena, former commander of the Fourth Infantry Brigade of El Paraíso; Colonel Rafael Flores Lima, ex-chief of the Joint General Staff; and Sergeant Mario Canizales Espinoza, of the Atonal Battalion.
The 89 year old Garcia was deported from the US in 2016 after a federal court found him guilty of serious violations of human rights prior to his entry to the US. He has also been linked to other civil war atrocities such as the massacre at El Mozote and the killing of four US churchwomen.
Judge María Mercedes Arguello also ordered that authorities begin an extradition process against Col. Mario Adalberto Reyes Mena, former commander of El Salvador’s 4th Infantry Brigade, who currently resides in the United States. Reyes Mena is alleged to have given the orders in 1982 to kill the four Dutch journalists. The massacre occurred in Santa Rita close to the base of the 4th Infantry Brigade in El Paraíso, Chalatenango.
Dutch journalists from ZEMBLA tracked Reyes Mena down through social media activity to a house in the United States. He has reportedly been living in the US since 1984, two years after the massacre. From NL Times :
Zembla tracked down the colonel who ordered the murder of the four Dutch. The now 79-year-old Mario Reyes Mena has been living in the United States for four years. Zembla found him through his three adult children, who are active on social media.
In 1993 a United Nations truth commission concluded that Reyes Mena was responsible for the ambush and the murder of the Dutch journalists – Koos Koster, Jan Kuiper, Joop Willemsen and Hans ter Laag. That same year an amnesty law was passed in El Salvador, which meant that he could not be prosecuted in that country.
The ZEMBLA team tweeted the video of meeting Reyes Mena at his front door where they asked to speak to him about the allegations in the Truth Commission report.
Reyes Mena is seen answering the door in an ARENA T-shirt and angrily telling the reporters that he was never charged with anything. The video begins in English and later their conversation switches to Spanish.
The families of the victims and the Dutch government have been seeking justice in this case throughout the past 40 years. As prospects for reopening the case brightened, they published a multimedia website in English and Spanish which presents the story of the massacre, the historical context and the quest for justice.
Dutch news outlets reported reactions to news of the arrests:
For Gert Kuiper, the brother of the murdered Jan Kuiper, the news about the arrests came as a big surprise. “It’s really good news, I’m hopeful that they will be brought to justice. These arrests give me hope that impunity will be nullified,” he told NOS. Kuiper is also happy that El Salvador is asking for the extradition of Colonel Reyes Mena, the leader of the unit that shot the Dutch. He left for the United States two years after the murders and still lives there. “The Americans can hardly let him live his life in Virginia unmolested,” says Kuiper.
Gert Kuiper and other relatives received the news about the arrests from their lawyers. Zembla reports that representatives of the Dutch Public Prosecution Service are going to El Salvador to speak with the suspects.
Advocates for the families held a press conference on Monday, October 17, to praise the actions of the court:
It is a very important case, considered as a crime against humanity, for which truth and justice have been demanded for 40 years. It is one of the crimes described in the report of the [UN] Truth Commission for El Salvador; thus we must recognize the courage of the judge,” said Oscar Pérez, president-director of Fundación Comunicarnos, an organization that, together with the Salvadoran Association for Human Rights (ASDEHU), is advancing the case in El Salvador.
October 19, 2022 Posted by aletho | Timeless or most popular, War Crimes | El Salvador | Leave a comment
The United States and Britain continue secret biological research in Central Asia
By Vladimir Platov – New Eastern Outlook – 19.10.2022
Despite numerous publications about military research in secret US biology laboratories in the post-Soviet space and demands to place their activities under strict international control, there is, unfortunately, no qualitative improvement of the situation in this matter. Therefore, it is not surprising that at the recent 22nd Meeting of the SCO Council of Heads of State, the Chinese president additionally drew the attention of the association’s member countries to the need “to effectively meet the challenges in biosecurity, and other non-traditional security domains”. As part of the Samarkand Declaration of 2022, SCO countries were urged to strictly adhere to the Biological Weapons Convention and to adopt a protocol to it that provides for an effective verification mechanism.
After Russia initiated the special operation to denazify Ukraine, alongside publicly exposing the illegal US biological weapons development activities in secret biolabs, the Pentagon sought to move unfinished programs in Ukraine to other countries in the post-Soviet region as quickly as possible. This particularly pertains to the territory of the states of Central Asia (CA) and Eastern Europe.
Recently, Russia Today journalists have found out that the US has decided to study the deadly anthrax in a bio-lab in Kyrgyzstan. In this regard, the US Department of Health & Human Services plans to fund this work and allocate about a quarter of a million dollars for this purpose. According to the tender published on the procurement portal of the US government, the regional hospital in the city of Osh in the south of the republic will become the base for these tests. At the same time, the publication reminded that Kyrgyzstan and the United States are negotiating a new agreement between the two countries in the field of US biological laboratories in the Republic of Kazakhstan, but the nuances and points of the future document are hidden from the public.
Very disturbing information in this regard has recently come from Uzbekistan, where, according to the Telegram channel, the active work of US representatives to create a powerful military-biological cluster in that country is confirmed. This is particularly evidenced by the growing “work” in Uzbekistan in recent years on the part of the US Agency for International Development (USAID) and the US Defense Threat Reduction Agency (DTRA). On this issue, the publication has prepared an infographic on US military-biological activities in Uzbekistan, which clearly indicates the potential damage to the security of the countries of Central Asia, the Russian Federation and China, the main political opponents of the White House.
There is also information that the United States and the United Kingdom continue to conduct joint research at the Kazakhstan Central Reference Laboratory (CRL) in Almaty. In early 2022, the United Kingdom shipped a large number of samples of virus strains, laboratory equipment, diagnostic instruments, etc. through the British shipping company WN Shipping the first half of the year.
Kazakhstan’s CRL in Almaty was built with Pentagon funds and has a third level of biohazard because a repository for particularly dangerous infectious agents is located on the premises of this facility, which are examined by staff of specialized laboratories for plague, cholera, zoonotic bacterial and natural viral focal infections. According to Kazakhstan’s official information, no US military experts (biologists and virologists) reportedly work at CRL, and as of January 1, 2020, it is fully funded and owned exclusively by Kazakhstan’s budget. However, in reality, this facility is not directly funded by the United States, but through a system of American grants, i.e. the research is carried out in the interest of the United States under a certain program of the Pentagon. And apparently this “cooperation” continues.
This is confirmed, in particular, by the fact that on November 5, 2021, the Ministry of Industry and Infrastructure Development of Kazakhstan initiated the process of public discussion on the construction project of the BSL-4 laboratory for work with especially dangerous strains and an underground storage facility for a collection of dangerous and especially dangerous strains in the village of Gvardeisky in the Zhambyl region, the construction of which is planned for 2025. The fourth biological safety code BSL-4 (Biosafety Level 4) of this planned biological laboratory alone indicates that the facility poses a high risk to people and society of the viruses being studied, most of which are simply impossible to handle.
The Kyrgyz public has already reacted very critically to this project. Protesters have gathered in front of the US Embassy, outraged that the lab will be built near the border with Kyrgyzstan, just 90 kilometers from Bishkek. Kyrgyz experts, together with the International Association for the Control of Biological Research, sent a letter this summer to the president of Kazakhstan, Kassym-Jomart Tokayev, asking that the construction of a biological laboratory in the border region be stopped.
Obviously, Washington is eager to preserve the countries of Central Asia as a testing ground for its military biological research. Hence the US efforts to develop similar projects in Uzbekistan, Kyrgyzstan, Kazakhstan and Tajikistan. At the same time, Washington has an increased interest in Tashkent and Alma-Ata, as these two countries have better developed infrastructure and more qualified personnel compared to other Central Asian states. The increased US interest in Uzbekistan is also due to the fact that the country is not a member of the CSTO, which gives Washington more freedom of action.
October 19, 2022 Posted by aletho | Timeless or most popular, War Crimes | Kazakhstan, Kyrgyzstan, UK, Ukraine, United States, Uzbekistan | Leave a comment
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