… And why didn’t he know it? Were his advisors concealing key information from him? Here’s what SHOULD have happened ….
A fascinating “what-might-have been” article published by The Brownstone Institute presents evidence that one White House meeting – later cancelled – might have prevented the lockdowns and much of the Covid madness that later ensued.
According to author Eric Hartmann, Stanford scientist Dr. John Ioannidis and a team of other “elite” scientists were set to meet with President Trump. The goal: Let the President know that every scientist didn’t think like Anthony Fauci and Deborah Birx.
(Ioannidis later became famous, or infamous, for showing that, for most citizens, the Infection Fatality Rate for this virus was roughly the same or lower than the death risk of the flu.)
The article’s salient points hinge on my favorite taboo subject – “early spread” – as Ioannidis is among the group who believed many Americans had probably already been infected by this virus by mid-March 2020.
This would mean any lockdowns to slow or stop the spread – or “flatten the curve” – were probably pointless and would cause far more harm than these draconian, unprecedented “mitigation” measures would prevent.
For me, the article also raises this intriguing question: What did certain officials know (about virus origins and spread) … and when did they know this?
Although my formal “science education” ended in 11th grade, my parents and God bestowed me with common sense, which I’m going to employ in today’s thought exercise, which shows what I would have done if I was Donald Trump or if I was the Science King of the World in the first 75 days of 2020.
Something like the events that follow SHOULD have happened in the pivotal, history-changing weeks of early 2020.
The fact something like this did NOT happen provides another giant tell about how corrupt and captured our science establishment has become.
I’m no scientist, but here’s what I would have done ….
The key “known knowable” in the “virus origins” saga is perhaps this nugget of information:
On the last day of December 2019, Chinese officials reported a pneumonia-like illness of “unknown origins” to the World Health Organization.
For the entire global “public health” establishment, this was a Super Bowl-type event.
“Okay, guys, this might be the Big One we’ve all been predicting. Let’s all get hot and prove our expert bonafides and save the world,” etc.
What would I have done when this news hit the Emergency Bat Wire?
First, I would have asked, “Okay, what are the symptoms of this alleged/possible new disease?”
Next, I would have asked: “Is it possible this possible new virus was already infecting people outside of Wuhan?”
Knowing the symptoms of this new disease are almost exactly like Influenza-Like Illnesses (ILI), I would have immediately started looking at all the weekly ILI “Surveillance Reports” produced by all 50 U.S. state health agencies and the CDC.
I would have asked: “Have we had a conspicuous spike of people going to the doctor with similar symptoms? For example, are people getting more flu tests than in previous flu seasons?”
As it turns out, as I showed in a recent article, the answer is/was, “Yes. No doubt.”
The next thing I would have done is told all my public health colleagues: “Guys, we need to develop an antibody assay to test for this new disease ASAP.”
After our crack scientists and medical labs had developed a suitable antibody test (China had one by late January 2020), I would have said: “We need to test ‘archived’ blood we already have in storage and see if any Americans had developed antibodies to this virus before, say, Dec. 30, 2019.”
My next Question: “Do we have any stored archived blood we can actually test for Covid antibodies?”
Answer: As it turns out, we do.
The Red Cross (and several other blood-bank organizations) actually collects tens of thousands of pints of blood every single day. One assumes at least some of this blood must be saved for weeks or months.
I would then order that we expedite the testing of every vial of “archived blood” in the country – Blood from California, Washington, New Jersey, Florida, Nebraska, Texas, Alabama – from all 50 states.
The whole purpose of this exercise would be to provide data and intelligence on how many people may have already been infected by this virus.
As Science King, I’d order that we use our invaluable new antibody-diagnostic tool to test samples collected from October 2019 through February 2020.
This way we could see if more blood donors in January had Covid antibodies than in November. If this was the case, we’d have what some might call “a virus-spread situation.”
Another point I would have made: Why do we have to depend on the Red Cross to provide us blood we can test for antibodies? We’re the U.S. Government; can’t we start collecting our own blood? Tell people it’s for a good cause – “Science.”
Apparently, the U.S. only had one batch of archived blood that could be tested ….
As readers of Bill Rice, Jr’s Substack Newsletter surely know by now, the CDC identified ONE tranche of saved Red Cross blood from three states, with that blood having been collected Dec. 13-16, 2019.
But surely this was not the only archived blood that had been saved and could have been tested (given that this was, after all, a “national emergency” – The Mother of All Live Exercises.)
But let’s say this was the only 1,900 vials of blood in the country available for antibody testing.
I would have said: “Okay, let’s at least go ahead and test that blood … but let’s test it as fast as we can …. Before we order the whole country to lock down.”
At some point, these 1,900 pints of Red Cross blood were tested for Covid antibodies, but, to this day, nobody knows WHEN these preserved blood specimens were tested. For all we know, that blood might have been tested by the end of February 2020 (weeks before the lockdowns were ordered) … or in September 2020, nine months after the blood had originally been collected.
All we know is the CDC (itself) published a “study” in late November 2020 telling everyone that at least 39 of those blood donors (2.04 percent of the tested cohort) did test positive for IgG (and/or IgM) antibodies via an ELISA antibody test.
So, to be clear, the dad-blasted virus was here – in at least three U.S. states in November 2019. That’s what the CDC’s own antibody test showed.
And President Trump – and Bill Rice, Jr. – could have known this by March 2020 if the Science officials had just put a “rush job” on the testing project. I mean, how long does it really take to test 1,900 units of blood for antibodies? Probably a couple of days.
I also note that the “Red Cross Antibody Study” results were published AFTER the 2020 presidential election – when the vaccine had already begun to be rolled out.
We also know (I think) President Trump wasn’t told anything like this in the weeks between January and March 2020:
“Mr. President, we’ve got a lot of blood we are currently testing to see if any Americans might have had this virus in November or December 2019. It’s possible, sir, this virus was already spreading pretty widely in America a couple of months ago. If this is the case, lockdowns to slow or stop virus spread probably won’t do much good.”
For what it’s worth, my conjecture is that SOMEONE in our Science/Virus-Fighting Leadership didn’t want the President (and/or the public) to know this non-trivial information.
Certainly nobody ordered any Red Cross archived blood to be tested as soon as possible.
(Also, just as certainly, no Cracker Jack investigative journalist at The New York Times, Wall Street Journal or “Sixty Minutes” asked any questions like: “Is there any evidence this virus has already been spreading around the world?”)
My main point is that nobody at NIH, NIAID, the HHS, the CDC or any member of the White House’s Covid Leadership Team said, “Let’s hold on here. Let’s see what these blood donor antibody tests tell us.”
When it came to locking down a couple billion people on the planet, why check any antibody test results first?
So what does this basic information tell us?
It tells me “someone” wanted to conceal evidence of early spread in America … that these trusted public health officials didn’t want to “confirm” anything that might stop or “call-off” the lockdowns.
… and, if we didn’t have the lockdowns, we might not have had 250 million Americans lining up to get a rushed, experimental” mRNA “vaccine,” a shot that was mandatory for many Americans if they wanted to keep their jobs or keep attending college.
Eric Hartmann’s article is about a White House meeting that did NOT take place, a meeting that might have changed history for the better if it had taken place.
Regarding Hartmann’s article, I’d simply highlight the topics that could and should have been brought up at said non-meeting … but weren’t … for some reason.
So what might this reason have been?
My strong hunch is that “someone” (or several people) knew, or at least strongly suspected, that this virus had already spread around the world, including America.
This prompts one final question: How in the hell could this person or people have known this?
It seems to me they knew what they didn’t want anyone to investigate. They didn’t want anyone to find undeniable evidence of early spread and then publicize said evidence to the entire world. Again, how did these people know or suspect what those investigations would have revealed?
June 24, 2023
Posted by aletho |
Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | CDC, Covid-19, COVID-19 Vaccine, HHS, NIAID, NIH |
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WASHINGTON – A group of Republican US House lawmakers are requesting info from New York City Schools Chancellor David Banks on the city’s practice of assigning “Problem Codes” to teachers who refused a COVID-19 vaccination and sending their data to the FBI, according to a letter sent by the lawmakers on Friday.
“I am writing to request greater information about the New York City Department of Education’s (NYCDOE) practice of assigning ‘Problem Codes’ to the records of New York City educators who lawfully chose not to receive COVID-19 vaccinations,” the letter said. “Moreover, the Department sent educators’ fingerprints to the Federal Bureau of Investigation (FBI) and the New York Criminal Justice Services.”
The letter was signed by House members including Representatives Nicholas Langworthy, Andrew Garbarino and Elise Stefanik.
Earlier this year, New York City officials incorrectly claimed that the Problem Codes are not part of a permanent personnel record and are not shared with any external organizations, the letter said.
Problem Codes were added to all employees who were placed on vaccine mandate leave, the letter said. The city used the same Problem Code for unvaccinated teachers as it uses for individuals accused of molesting, raping or harming a child, the letter said.
The Problem Codes can have a “profoundly negative impact” on flagged educators and can hinder their future employment prospects, the letter said. Educators are often unaware they have been flagged until they face employment rejections elsewhere, the letter said.
“City Hall’s false and misleading statements regarding the existence, nature, utilization, and impact of Problem Codes on teachers’ livelihoods cannot be accepted at face value. The City has been less than forthcoming about the Problem Codes issued to educators,” the letter said.
The lawmakers are requesting that Banks provide them with information on the purpose and utilization of Problem Codes by the city, explain discrepancies in their claims and clarify the transfer of fingerprint information to law enforcement, according to the letter.
The letter also requests information on what measures may be taken to rectify any “unjust consequences” faced by educators as a result of the Problem Codes, as well as whether the city has any plans to revise their practices.
June 23, 2023
Posted by aletho |
Civil Liberties | COVID-19 Vaccine, Human rights, New York City, United States |
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Documents released by BioNTech to the European Medicines Agency (EMA) reveal tens of thousands of serious adverse events and thousands of deaths among people who received the Pfizer-BioNTech mRNA COVID-19 vaccine.
The documents, dated Aug. 18, 2022, and marked “confidential,” show that cumulatively, during the clinical trials and post-marketing period up to June 18, 2022, a total of 4,964,106 adverse events were recorded. The documents included an appendix with further details about the specifics about the identified adverse events.
Among children under age 17, 189 deaths and thousands of serious adverse events were reported.
The documents present data collected between Dec. 19, 2021, and June 18, 2022 (the “PSUR #3 period”), in addition to cumulative data on adverse events and deaths that occurred among those who received the vaccine during clinical trials and during the post-marketing period, beginning December 2020 up until June 18, 2022.
During this time, Pfizer-BioNTech said it identified almost no safety signals and claimed the vaccine demonstrated over 91% “efficacy.”
Remarking on the documents, Brian Hooker, Ph.D., P.E., senior director of science and research for Children’s Health Defense, told The Defender :
“These adverse event reports are ‘off the charts,’ with myocarditis reports at over 10,000 and pericarditis reports at over 9,000.
“Historically, we know that this would be an under-ascertainment of the actual numbers. It is criminal for the EMA to keep this vaccine on the market.”
According to an analysis by commentator and author Daniel Horowitz, the percentage of adverse events classified as serious was “well above the standard for safety signals usually pegged at 15%,” and women reported adverse events at three times the rate of men.
Sixty percent of cases were reported with either “outcome unknown” or “not recovered,” suggesting many of the injuries “were not transient,” Horowitz said.
The highest number of cases occurred in the 31-50 age group, of which 92% did not have any comorbidities, making it very likely it was the vaccine causing “such widespread, sudden injury.”
There were 3,280 fatalities among vaccine recipients in the combined cumulative period including the clinical trials and post-marketing, up to July 18, 2022.
According to Horowitz, the documents “show that Pfizer knew about a sickening level of injury early on,” yet continued to distribute its COVID-19 vaccine.
The documents are not part of the ongoing court-ordered release of the so-called “Pfizer documents” in the U.S., but according to Horowitz, are pharmacovigilance documents requested by the EMA, the EU’s drug regulator.
The documents were made available to an Austrian science and politics blog, TKP, following “a FOIA [Freedom of Information Act] request from an anonymous reader.” They were subsequently published on March 4. However, once published, no European English-language media outlet appears to have reported on them.
As a result, they remained under the radar until recently, when several independent English-language bloggers discovered and published the documents.
Thousands of pediatric serious adverse events and deaths
The main Pfizer-BioNTech document revealed 9,605 adverse events (3,735 serious) during the PSUR #3 and 25 cases during the clinical trials among children ages 11 and younger. These included 20 fatalities, in children as young as 5 years old.
Causes of these fatalities included dyspnea, cardiac arrest, cardio-respiratory arrest, pyrexia and myocarditis, though “all events were assessed as unrelated” to the vaccine.
In one example listed in the document, an 11-year-old boy died of acute respiratory failure two days after the first dose of the vaccine. In another case, a 6-year-old girl died seven days following her initial dose of complications that included renal impairment, epilepsy, apnea, seizure and “sudden death.”
The document lists another case, that of a 6-year-old boy whose listed causes of death are myocarditis, cardio-respiratory arrest and COVID-19. He died seven days after the first dose of the vaccine, and although autopsy results were “pending,” “the reporter concluded that the death ‘had nothing to do’ with the administration of BNT162b2 [the Pfizer-BioNTech vaccine] and was due to natural causes.”
For children ages 12-17, the document listed 21,945 adverse eventss (19,558 serious) in the post-marketing period and 15 cases during clinical trials. A total of 169 deaths were recorded, with listed causes including dyspnea, pyrexia, cardiac arrest, myocarditis, cardiac failure, seizure and shock.
Nevertheless, the document states “No new significant safety information was identified based on the review of the cases reported in the overall paediatric population.”
‘No safety signals’ despites deaths, injuries of pregnant women and newborns
Pregnant and lactating women also were significantly affected. There were 3,642 post-authorization adverse events and 697 clinical trial adverse events in this population, including spontaneous abortion, fetal death, postpartum hemorrhage, premature separation of the placenta, premature labor or delivery, live birth with congenital anomalies and stillbirths.
Nevertheless, the documentation again states, “There were no safety signals regarding use in pregnant/lactating women that emerged from the review of these cases or the medical literature,” despite two key admissions elsewhere in the documentation.
In one instance, the document stated, “The safety profile of the vaccine in pregnant and/or breastfeeding women was not studied in the pivotal clinical trial and the maternal clinical trial was terminated early due to participant recruitment difficulties.”
And in another instance, Pfizer-BioNTech identified the following as “missing information”:
“Use in pregnancy and while breastfeeding; Use in immunocompromised patients; Use in frail patients with co-morbidities … Use in patients with autoimmune or inflammatory disorders; Interaction with other vaccines; Long term safety data.”
Pfizer-BioNTech stated a “commitment” to track “pregnancy outcome[s] in clinical trials.”
Myocarditis and pericarditis deaths among children, young adults
A notable discrepancy appears in terms of reported cases of myocarditis in the clinical trials as compared to the post-marketing period — one myocarditis case (0.15% of all cases) is listed for the clinical trial period, while 5,422 cases (1.1% of all cases) and 5,458 serious events were reported in the PSUR #3 period.
Of these, 87 cases were fatal and 1,608 were listed as “not resolved.” Among children and young adults, 48 cases were reported for those between the ages of 5 and 11 (two deaths), 366 among 12-15-year-olds (three deaths), 345 among 16-17-year-olds and 968 among 18-24-year-olds (four deaths).
In one instance, an 11-year-old girl developed myocarditis two days after her first dose and subsequently died, with the listed causes of death including myocarditis, respiratory failure, acute cardiac failure and cardio-respiratory arrest.
Separately, a 13-year-old boy developed myocarditis five days after his second dose, and subsequently died of myocarditis, cardiac arrest, multiple organ dysfunction syndrome, ventricular tachycardia and renal failure.
A 13-year-old girl with no medical history developed myocarditis six days after her first dose and also later died.
In the case of a 19-year-old male who developed myocarditis three days after his third dose and who eventually died, an autopsy “revealed extensive necrosis of the left ventricular myocardium (myocardial necrosis); myocarditis/fulminant myocarditis.”
And a 26-year-old male who also took the flu vaccine developed myocarditis four days after his third dose of the Pfizer-BioNTech COVID-19 vaccine, and subsequently died. The listed causes of death included myocarditis, arrhythmia, inflammation and left ventricular dysfunction. Autopsy results “showed myocarditis.”
Similarly, while no cases of pericarditis were recorded during the clinical trial, 4,156 were recorded during the PSUR #3 period, including 4,164 serious adverse events and 19 fatalities. This included 30 cases among 5-11-year-olds, 118 cases among 12-15-year-olds, 106 cases among 16-17-year-olds, 479 cases among 18-24-year-olds (and one death), and 417 cases among 25-29-year-olds, again including one death.
In one example, a 22-year-old male developed pericarditis 31 days after his second dose and eventually died of pericarditis and other causes, including multiple organ dysfunction syndrome, pericardial mass, pericardial effusion, malignant pericardial mesothelioma and right ventricular failure.
Numerous other cardiovascular adverse events were recorded, totaling 32,712 cases during the PSUR #3 period (496 fatal) and 27 during the clinical trials (two fatal — with none of the events listed as “related” to vaccination).
Causes of death included in this category include arrhythmia, cardiac failure and acute cardiac failure, cardiogenic shock, coronary artery disease, postural orthostatic tachycardia syndrome (POTS) and tachycardia.
Nevertheless, “No new significant safety information was identified.”
Many ‘very severe and very rare’ adverse events identified
The 393-page confidential Pfizer document shows that Pfizer observed more than 10,000 categories of diagnosis, many “very severe and very rare,” Horowitz wrote.
These include 73,542 cases of 264 categories of vascular disorders from the shots, many of which “are rare conditions,” hundreds of categories of nervous system disorders, totaling 696,508 cases and 61,518 adverse events from well over 100 categories of eye disorders, “which is unusual for a vaccine injury,” according to Horowitz.
In addition, “there were over 47,000 ear disorders, including almost 16,000 cases of tinnitus,” “roughly 225,000 cases of skin and tissue disorders,” “roughly 190,000 cases of respiratory disorders” and “over 178,000 cases of reproductive or breast disorders, including disorders you wouldn’t expect, such as 506 cases of erectile dysfunction.”
“Over 100,000 blood and lymphatic disorders, for both of which there’s a wealth of literature linking them to the spike protein” were indicated, as well as “almost 127,000 cardiac disorders, running the gamut of about 270 categories of heart damage, including many rare disorders, in addition to myocarditis.”
There were also “3,711 cases of tumors — benign and malignant,” and “there were over 77,000 psychiatric disorders observed.”
“What is so jarring is that there are hundreds of very rare neurological disorders that reflect something so systemically wrong with the shots, a reality that was clearly of no concern to the manufacturers and regulators alike,” Horowitz wrote, referencing 68 listed cases of a rare diagnosis, chronic inflammatory demyelinating polyneuropathy.
In another example, the “Pharma Files” Substack identified 3,092 neoplasms, noting that ”malignant neoplasms means cancer.”
Pfizer-BioNTech usually identified ‘no safety signal’ despite thousands of deaths
Numerous deaths and serious adverse events were recorded for a wide range of other conditions:
- Stroke: 3,091 cases and 3,532 serious adverse events during PSUR #3, including 314 fatalities, and 19 cases during the clinical trial (one death).
The document stated, “Cerebral venous sinus thrombosis … and Cerebrovascular Accident/Stroke were evaluated as signals during the reporting period and were not determined to be risks causally associated with the vaccine … No additional safety signals … have emerged based on the review of these cases.”
- Respiratory: 2,199 cases and 1,873 serious adverse events during PSUR #3, including 363 fatalities, and 33 cases during the clinical trial (four deaths). Serious adverse events included cardio-respiratory arrest, pneumonia, respiratory failure, acute respiratory failure, hypoxia and acute respiratory distress syndrome. Yet, “No safety signals have emerged based on the review of these cases.”
- Bell’s palsy: 733 cases were reported during PSUR #3, in addition to 1,428 cases of facial paralysis. Six cases were fatal, with all victims over age 60. One additional case of Bell’s palsy, in a 75-year-old female from the U.S., was recorded in the clinical trial but was deemed “not related” to her vaccination. Again, “No new significant safety information was identified.”
- Neurological: 5,111 cases and 4,973 serious adverse events during PSUR #3, including 67 fatalities, and 15 cases during the clinical trial. Once more, “No safety signals have emerged based on the review of these cases.”
- Immune-mediated/autoimmune adverse events: 11,726 cases and 8,445 serious adverse events during PSUR #3, including 133 fatalities, and 19 cases during the clinical trial. Serious adverse events included thrombocytopenia, interstitial lung disease, cerebral hemorrhage, encephalitis, multiple organ dysfunction syndrome, renal failure, pneumonia and pulmonary embolism. Yet, “No new safety signals have emerged.”
- Multisystem inflammatory syndrome: 207 cases and 210 serious adverse events during PSUR #3, including 56 deaths, with 35 involving the elderly. In addition, 38 cases were reported in children. Nevertheless, “No new safety signals have emerged based on a review of these cases [or] literature.”
Pfizer-BioNTech stated a “commitment” for “closely monitoring multisystem inflammatory syndrome in children and in adults … and reporting of new cases.”
- Thromboembolic adverse events: 6,102 cases and 6,724 serious adverse events during PSUR #3, including 265 fatalities, and 17 cases during the clinical trial (one death). Serious adverse events included pulmonary embolism, thrombosis and deep vein thrombosis. Again, “No safety signals have emerged based on the review of these cases.”
Elsewhere in the document, the case of a 14-year-old male who died of peripheral swelling after getting the COVID-19 vaccine was mentioned, with no additional details.
In another example, a 67-year-old male “with a history of diabetes and idiopathic thrombocytopenic purpura” suffered chest and gastrointestinal discomfort less than 30 minutes after receiving his third dose of the vaccine. A diagnosis of anaphylaxis was made, while an electrocardiogram showed “signs of a myocardial infarction.” He later sustained cardiac arrest and died 12 days following his vaccination.
Moreover, 204 fatalities (and 24,077 cases) of vaccination failure, 81 deaths from “vaccination stress,” 24 deaths (and 1,402 cases) of suspected vaccination failure, two deaths from glomerulonephritis and nephrotic syndrome, two deaths (1,326 cases) from “medication error” and 166 deaths from “other” adverse events — mostly pyrexia — were recorded.
Pfizer-BioNTech and EMA: ‘nothing to see here’
Pfizer and BioNTech claimed that the overall efficacy of their COVID-19 vaccine for the PSUR #3 period was 91.3% — and 100% for some populations.
Moreover, only one safety signal was definitively identified: hearing loss, with Pfizer-BioNTech committing to perform a “safety evaluation of tinnitus and hearing loss.”
Two other conditions, myocarditis and pericarditis, were determined to be an “important identified risk,” while irritability was determined to be an “identified risk (not important).”
“A statement regarding the reporting rates of myocarditis and pericarditis after primary series and booster doses” was added to their vaccine’s European product label.
Labeling was changed for Guillain-Barré syndrome, but in Japan. The document stated:
“Although not considered by definition a regulatory action taken for safety reasons because it does not significantly impact the benefit risk balance of use of the product in authorised populations, due to the receipt of spontaneous reports of Guillain-Barre syndrome (GBS) after vaccination with mRNA COVID-19 vaccines including BNT162b2 … Japan has required class changes to include GBS in the important precautions section of the Japan package insert.”
Despite the large number of deaths and serious adverse events, Pfizer and BioNTech wrote, “Based on the available safety and efficacy/effectiveness data from the reporting interval for BNT162b2, the overall benefit-risk profile of BNT162b2 remains favorable” and that “no further changes … or additional risk minimization activities are warranted.”
The EMA appears to have agreed with this conclusion. In its “assessment report,” its Pharmacovigilance Risk Assessment Committee (PRAC) wrote that “The benefit-risk balance for the use of Comirnaty in its authorized indication remains unchanged.”
“The PRAC considers that the risk-benefit balance of medicinal products containing tozinameran (Comirnaty) remains unchanged and therefore recommends the maintenance of the marketing authorisation(s),” the PRAC added.
However, Horowitz argues that the documents “show that Pfizer knew about a sickening level of injury early on,” yet continued to distribute its COVID-19 vaccine.
Earlier this month, BioNTech was sued in Germany by a woman alleging injuries from the Pfizer-BioNTech COVID-19 vaccine. The lawsuit demands at least 150,000 euro ($161,500) in damages for bodily harm and unspecified compensation for material damages.
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.
June 23, 2023
Posted by aletho |
Deception, Timeless or most popular, War Crimes | COVID-19 Vaccine, European Union, Pfizer |
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When it comes to error correction, the USA’s 50 sovereign states offer more opportunity for an authoritative challenge to the misuse of power than we enjoy in the UK. Dr Joseph Ladapo, the Florida Surgeon General, has made public a letter excoriating federal health officials over their promotion of the mRNA Covid vaccines. The government, he said, ‘has relentlessly forced a premature vaccine into the arms of the American people with little or no concern for the adverse ramifications’.
The letter was to Drs Robert Califf, head of the Food and Drug Administration, and Rochelle Walensky, director of the Centers for Disease Control and Prevention. Lapado wrote: ‘Your ongoing decision to ignore many of the risks associated with mRNA Covid-19 vaccines, alongside your efforts to manipulate the public into thinking they are harmless, have resulted in deep distrust in the American health care system.’
As reported here earlier this year, senior American scientists have called for a ‘bipartisan, scientifically minded Covid-19 commission so the public health disaster of the past three years is not repeated’. They face an uphill struggle in achieving that aim, but Ladapo’s no-holds-barred letter means that at least some of Florida’s 22.6million citizens have a chance of knowing the jabs are not ‘safe and effective’, as the British public are constantly being told.
Ladapo would surely have been less forthright if Ron DeSantis, Florida’s Republican governor and a possible future US president, were not also on the warpath over the Biden administration’s handling of the pandemic. The Florida Supreme Court has approved DeSantis’s request to convene a grand jury to investigate ‘wrongdoings’ associated with the vaccines.
But DeSantis is not alone. The Texas Attorney General has launched an investigation into whether Pfizer, Moderna and Johnson & Johnson, the companies producing the jabs, misrepresented their safety and efficacy and manipulated trial data. The investigation could open the door to lawsuits by people injured by the mRNA products.
Meanwhile, what hope of redress do Britons have, not just for vaccine damage but for the lives shattered by cruel and unprecedented lockdowns?
The public inquiry led by Baroness Hallett looks likely to be worse than useless, as Laura Dodsworth, author of the best-selling A State of Fear: How the UK Government Weaponised Fear During the Covid-19 Pandemic, has described.
It is in ‘the wise and noble tradition of the great British public inquiry’, Rod Liddle commented in the Sunday Times last weekend. That is, keep the public away from it for as long as possible, and say nothing useful or meaningful unless ‘at least 20 years after whatever it is that they are inquiring about, at which point most of the relevant people are stiff as a stoat’.
The headline on Liddle’s article declared: ‘The data is clear: lockdowns are useless. But you won’t hear that from the inquiry.’
Sadly, neither the Sunday Times nor its daily stablemate, nor just about any of the mainstream media in the UK, have yet ventured into questioning the ‘safe and effective’ narrative about the vaccines. So let’s look at what Ladapo, who as state surgeon general can hardly be dismissed as a conspiracy theorist, has told the American public.
‘Data are unequivocal,’ Ladapo wrote. ‘After the Covid-19 vaccine rollout, the Vaccine Adverse Events Reporting System (VAERS) reporting increased by 1,700 per cent, including a 4,400 per cent increase in life-threatening conditions.
‘Dismissing this pronounced increase as being solely due to reporting trends is a callous denial of corroborating scientific evidence also pointing to increased risk and a poor safety profile. It also fails to explain the disproportionate increase in life-threatening adverse events for the mRNA vaccines compared to all adverse events.
‘Based on the CDC’s own data, rates of incapacitation after mRNA vaccination far surpass other vaccines.’
Ladapo cited a recent study which found an excess risk of serious adverse events ‘of special interest’ for 1 in 550 people after mRNA vaccination. He wrote: ‘As you are aware, this is extraordinarily high for a vaccine. In comparison, the risk of serious adverse events after influenza vaccination is much lower. For you to claim that serious adverse events such as these are “rare” when Pfizer and Moderna’s clinical trial data indicate they are not, is a startling exercise in disinformation.
‘I want to re-emphasise that these questions could have been answered if you had required vaccine manufacturers to perform and report adequate clinical trials . . . I anticipate with regret that you will repeat past mistakes and prematurely promote new therapies to Americans without accurately and truthfully weighing data on risks and benefits.’
Ladapo then asked Califf and Walensky to answer 12 questions relating to the safety data, and concluded: ‘Your organisations are the main entities promoting vaccine hesitancy – Florida promotes the truth. It is our duty to provide all information within our power to individuals so they can make their own informed health care decisions. A lack of transparency only harms Americans’ faith in science.’
Regular readers of TCW as well as The Daily Sceptic know that numerous scientists support Ladapo’s position, such as reported here, here, here, here, here, here and here.
At present, however, the FDA and CDC, like the NHS, continue to ignore such reports, asserting that ‘the known and potential benefits of these vaccines clearly outweigh their known and potential risks, and that ‘being up to date on vaccinations saves lives compared with individuals who did not get vaccinated’.
June 23, 2023
Posted by aletho |
Science and Pseudo-Science | CDC, COVID-19 Vaccine, FDA, NHS, UK, United States |
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One of the remarkable features of these Covid years is the amount of misleading and downright false information emitted by “official” sources, most notably public health authorities, government-appointed regulators, and mainstream media. A part of me hankers after the times when I could trust my government and media in a time of crisis. But if I am honest with myself, I have to admit that I’d prefer to live uncomfortably in the truth than comfortably in a fantasy built for me by someone who does not have my best interests at heart.
As somone who turned on a daily basis to the website of the Centre for Disease Control and Prevention for updates on the Covid outbreak in February and March 2020, I was especially shocked and disappointed by the abysmal failure of authoritative bodies to impartially report the evidence bearing on masking, vaccinations, lockdowns, PCR testing, and other aspects of pandemic policy. My whole faith in the political, media, and scientific establishment, limited as it was, was shaken to the core.
We have been betrayed by the people charged with sharing the best available data and information with us in a time of crisis. We have been lied to and deceived about matters of life and death, such as the risk-benefit tradeoffs of the Covid vaccines, not only by the pharmaceutical industry, but by the people who occupy leading positions of public authority in our society.
Our politicians have sold us “solutions” to Covid that were far, far worse than the disease, and have generally refused to admit to their mistakes, even when they saw the comparative success of regimes like Sweden and Florida that went a very different direction.
Among the more egregious falsehoods that were either stated or implied by official authorities, and uncritically echoed by mainstream media, are the following:
- the notion that community masking was supported by strong scientific evidence. It never was (here is the latest Cochrane review of evidence for mask efficacy).
- the idea that it was critical that young and health people get vaccinated, if not for themselves, then for the sake of “granny and granddad.” This idea was empirically baseless, since we did not have any good evidence to show that these vaccines prevented transmission at the time these claims were made.
- the idea that toddlers and young children and teenagers with no serious health issues could benefit from receiving a Covid vaccine. There is absolutely no evidence to suggest that children’s risk from Covid is significant enough to warrant their exposure to a vaccine that has sparked a significant number of adverse events and whose long-term risks to children are still not well understood.
- the idea that sheltering in place for months on end would effectively stop a respiratory virus from spreading through the community, rather than just deferring the inevitable and inflicting enormous social and human costs in the meantime. This was a dangerous and revolutionary proposition that had no strong empirical evidence to support it.
- The idea that a person who tested positive in a PCR test, but had absolutely no clinical symptoms of Covid-related disease, should count as a Covid “case” or that the death of such a person was a “Covid” death.
I could go on, and talk about the use of a handful of cases of infant hospitalisation to push vaccines on children, the unnecessary and counterproductive closure of schools, the US government’s active role in encouraging private social media companies, behind the scenes, to censor their critics, or the infamous Hancock files, which uncover the UK’s Health Secretary Matt Hancock’s plan to “scare the pants off everyone” with his announcement of the next “variant” of Covid-19.
Thoughtful citizens who notice these betrayals now have strong grounds for distrusting “official” sources to tell them the truth, or present the facts in a non-manipulative, impartial manner. For me, and many others, the old idea that you could depend on your government to inform you of the latest science or tell you the threat level of a disease is now dead in the water.
Put simply, we now live in an informational No Man’s Land, in which every man must fend for himself, to the best of his ability, without the backing of an impressive Official Source to do his thinking for him.
We each have to scrape together whatever information we can from unofficial sources that have gotten important things right and are not defending the indefensible: coerced vaccination, vaccine-based segregation, involuntary population-wide lockdowns, etc.
It puts many of us in the peculiar position of placing more weight on the words and recommendations of individual journalists and scientists whose character and intellect we trust, than the pronouncements of national governments, official regulators, or international bodies like the World Health Organisation.
Living in an informational No Man’s Land is demanding because you can’t just skip over to the CDC website to resolve your doubts. And it is uncomfortable because you do not enjoy anything like the level of faith the average citizen has in “Science” and “Officialdom.” You are sort of at sea, and you cling to whatever bits of information and insight you can scavenge from sources that are not living off the proceeds of vaccine sales or paid by governments to launch sophisticated campaigns of psychological warfare against their own citizens.
The painful truth is that official “experts” and government ministers have played god with our lives and repeatedly given dangerous and scientifically baseless advice.
Under these circumstances, those who do their own independent research, rather than uncritically swallowing whatever “official authorities” tell them, are not the “cranks” and “conspiracy theorists” they are being made out to be, but citizens who actually understand the predicament they find themselves in, and have the courage to think for themselves, even when it draws down ridicule, censorship, and alienation from “respectable” society.
June 23, 2023
Posted by aletho |
Deception, Science and Pseudo-Science, Timeless or most popular | Covid-19, COVID-19 Vaccine |
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Looking at the COVID pandemic as a military-run operation puts public laws and documents into light while painting a different picture of the whole was really in charge of the US response. Was this martial law?
June 23, 2023
Posted by aletho |
Civil Liberties, Timeless or most popular, Video, War Crimes | Covid-19, COVID-19 Vaccine, United States |
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In simpler times, a dichotomy was understood to exist whereby our newspapers of record printed The Truth while those on the other side regurgitated state propaganda. It is of course a conceit, as the complicity of our mass media in pushing the party line on Covid-19 over the last three years demonstrates, but it’s one of which all journalists, and especially those in the business of conducting investigations, should be ever mindful or they risk being bamboozled.
On June 10, a headline in the Sunday Times promised to inform its readers ‘What really went on inside the Wuhan Lab weeks before Covid erupted’. The lengthy story was by Jonathan Calvert and George Arbuthnott, editor and deputy editor of ‘the renowned Insight investigative team’.
Insight said they had ‘reviewed hundreds of documents, including previously confidential reports, internal memos, scientific papers and email correspondence that has been obtained through sources or by freedom of information campaigners in the three years since the pandemic started. We also interviewed the US State Department investigators – including experts on China, emerging pandemic threats, and biowarfare – who conducted the first significant US inquiry into the origins of the Covid-19 outbreak’.
The facts presented by the Insight team are accurate as far as they go: the Wuhan Institute of Virology (WIV) received funding in 2009 from the US non-profit organisation EcoHealth Alliance and was collecting bat coronaviruses to identify pandemic potential viruses as part of a programme called PREDICT. https://p2.predict.global/ WIV received more money from the US National Institutes of Health (NIH) via EcoHealth Alliance in 2014 to continue its bat coronavirus research. The American Defense Advanced Research Projects Agency (DARPA) refused to fund an EcoHealth Alliance proposal called DEFUSE in 2018, part of which proposed genetically engineering bat coronaviruses to see if they could be made more infectious to humans by adding what is called a ‘furin cleavage’ gene.
What the Sunday Times does not make clear is that the PREDICT programme in which EcoHealth Alliance was a partner was launched by the US government Agency for International Development (USAID) in 2009. It continued work started by the US military in the early 1960s to support military preparedness by identifying infectious diseases which might trouble US forces abroad. Under PREDICT this research was in effect rebranded as civilian work by identifying pandemic potential viruses which threatened to jump from animals to humans. To use the terminology of the Cold War, EcoHealth Alliance was acting as a ‘cut-out’ – a front – for the CIA-linked USAID. Nor does the Sunday Times make clear that the National Institute of Allergy and Infectious Diseases (NIAID), then headed by Dr Anthony Fauci, funded the DEFUSE programme rejected by DARPA, or that Dr Ralph Baric, a coronavirus expert at the University of North Carolina and WIV collaborator, who they note had himself been mixing genes from different pathogens to make chimeric viruses, wrote the gain-of-function section of the proposal.
If the meaning of ‘insight’ is to gain an accurate and a deep understanding of something, these details are more than incidental. Deep understanding requires sceptical interrogation of both the source material and the purpose behind the production of material such as ‘previously confidential reports’. It is here that things start to go awry for the Sunday Times.
Most quotes in the story are attributed to anonymous US ‘sources’ linked to a 2020 US State Department investigation into Covid-19’s origins. The reader is expected to accept their credibility at face value because they come from ‘our’ side. The only two on-record sources linked to the investigation are scientists Dr Richard Ebright, a longstanding critic of gain-of-function research, and Dr Steven Quay, the CEO of a biotechnology company.
It’s unclear who else the Sunday Times interviewed but amongst those involved in the State Department investigation was David Asher of the Hudson Institute, which is the ‘fiscal sponsor’ of the Bipartisan Commission on Biodefense established by Dr Robert Kadlec in 2014 when he was a mere lobbyist for the vaccine manufacturer Emergent Biosolutions. Kadlec is the principal architect of 21st century US biosecurity policy. The Commission produced the draft blueprint for Kadlec’s revamped National Biodefense Policy which was adopted by President Trump in 2018.
The investigation was set up when the State Department was led by the China hawk, Mike Pompeo, who favoured a more robust foreign policy which treated China as a dangerous strategic competitor for global hegemony. His department began exploring an alternative explanation for the emergence of Covid-19 from the natural spillover notoriously articulated in the 2020 ‘proximal origin’ paper. The far-from-disinterested parties, Dr Anthony Fauci, Sir Jeremy Farrar, then director of the UK Wellcome Trust and now WHO chief scientist, Dr Ralph Baric and Dr Peter Daszak, the chief executive of Ecohealth Alliance, were all involved in an email chain with the authors discussing the natural spillover framing in advance of the paper’s publication.
In January 2021, days before the end of Donald Trump’s Presidency, Secretary of State Pompeo issued a press release ‘sharing new information concerning the activities inside China’s government laboratories in 2019’ and demanding the World Health Organization investigate the origins of Covid-19 which he was suggesting arose from Chinese military bioweapon research at the WIV.
The US ‘had reason to believe’, said Pompeo, that several WIV researchers became sick in the autumn of 2019 and had ‘symptoms consistent with both Covid-19 and common seasonal illnesses’. He then said the WIV was studying RaTG13, the bat coronavirus which was most similar to SARS-CoV-2, while conducting possible ‘gain-of-function’ experiments to enhance transmissibility or lethality. Pompeo omitted to mention that the US government had outsourced all this bat-related research to WIV before sensationally claiming that WIV, despite claiming to be a civilian research institution, had secret links to the Chinese military and had been doing research for them since 2017. He accused China of behaving irresponsibly by withholding ‘vital information that scientists need to protect the world from this deadly virus, and the next one’.
The State Department investigation Pompeo initiated didn’t die with the Trump administration. The work was continued by someone the Sunday Times article mentions in passing as responsible for the US vaccine development programme, Dr Robert Kadlec.
After his tenure as Assistant Secretary for Preparedness and Response ended, Dr Bob was hired once again by his old friend Senator Richard Burr to work for the GOP minority on the Senate HELP Committee. Burr had in fact recommended Kadlec to President Trump for the role of Assistant Secretary for Preparedness and Response (ASPR), an office within Health and Human Services, the pulpit from which he was finally able to fulfil his ambitions for his vaccine ‘Manhattan Project’.
Kadlec’s account ‘Muddy Waters: The origins of Covid-19 report’ was published in April 2023. It is straight out of the playbook of Britain’s favourite fictional civil servant Sir Humphrey Appleby, who pithily observed: ‘Clarification is not to clarify things. It’s to put oneself in the clear.’
The report, co-authored by Dr Bob Foster, a former chief scientist for Medical Systems Integration at Fort Detrick, the US Army Medical Research Centre, runs to 300 pages and contains 1,570 citations. Kadlec, who was once a weapons inspector deployed to Iraq to find non-existent biological weapons of mass destruction, is up to his old tricks again. The thesis put forward is the long version of the January 15, 2021, Pompeo press release. They contend that SARS-CoV-2 was circulating in the autumn of 2019, that it had leaked from the WIV lab and that because a People’s Liberation Army vaccine specialist, Zhou Yusen, a decorated military scientist, filed a patent for a vaccine in February 2020, China must have known about the leak in November. They deduce from all this that China’s military was secretly working with the WIV to develop simultaneously a bioweapon and a vaccine.
For all the material they say they reviewed, the Sunday Times writers unquestioningly retell the account given in Muddy Waters: ‘The investigators believe the Chinese military had taken an interest in developing a vaccine for the (corona)viruses so they could be used as potential bioweapons. If a country could inoculate its population against its own secret virus, it might have a weapon to shift the balance of world power.’
It’s beyond the scope of a brief article to rebut the entire document, but let me give you the flavour of it using two pieces of evidence put forward in the Muddy Waters report.
According to the report: ‘On November 25, 2019, a 25-year-old Welsh teacher in Wuhan fell ill with flu-like symptoms. The teacher developed pneumonia on December 6, 2019 and was hospitalised. On January 16, 2020, the hospital informed the teacher by letter that he had been infected by the novel coronavirus.’
The citation for this is a March 4 2020 Daily Mail interview with the teacher, Connor Reed, who lived to tell the tale. When he felt ill, Reed took a taxi to Zhongnan University Hospital because he wanted to see a British doctor and ‘there are plenty of foreign doctors there, studying’. He was diagnosed with pneumonia and sent home that evening with antibiotics which he says he didn’t take, preferring instead to use Tiger Balm. It’s a far cry from most people’s understanding of ‘hospitalised’.
The evidence for a lab leak is just as dodgy. The Sunday Times reported that the investigators believed that researchers working in the WIV coronavirus lab became sick in the second week of November. They say an investigator told them: ‘We were rock-solid confident that this was likely Covid-19 because they were working on advanced coronavirus research in the laboratory of Dr Shi. They’re trained biologists in their thirties and forties. Thirty-five-year-old scientists don’t get very sick with influenza.’
The citation in Muddy Waters for the story about the sick WIV researchers leads to Josh Rogin, foreign policy reporter for the Washington Post, who says that his information came from secret intelligence gathered by the US Government.
Current discussions of Covid’s origin proffer two explanations: a bioweapon accidentally released from an unsafe laboratory versus a naturally occurring spillover from animal to humans. Neither explanation can account for why Moderna, a company with close links to the US government which has been generously funded by the US government agencies DARPA and the Biomedical Advanced Research and Development Authority (BARDA), began making contractual preparations for its coronavirus vaccine in May 2019 when it asked Merck to give up the exclusivity provision in its 2015 Master Collaboration Agreement with respect to a ‘specific set of respiratory infections’. Nor can it account for the fact that Moderna’s prototype coronavirus vaccine was sent to Baric for animal testing on December 16, 2019, two weeks before the Chinese reported a ‘pneumonia of unknown origin’. The binary nature of the origin discussions obscures other possibilities, such as the one suggested by the Iranians in March 2020 and thereafter ignored, that Covid-19 was an American bioweapon, a scenario under which it’s plausible that the researchers at WIV were intentionally set up to take the blame.
As for the Sunday Times, on this occasion it has conveyed no insight, only American propaganda designed to muddy the waters, not clarify them.
June 22, 2023
Posted by aletho |
Deception, Timeless or most popular, War Crimes | China, Covid-19, COVID-19 Vaccine, United States |
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Quick Hits on Jerrold Nadler, Rochelle Walensky, Demar Hamlin, Jamie Foxx, Kathy Huchul, and Propagandized “Misinformation”
Among all the independent media superstars, Joe “Pags” Pagliarulo does one of the best “rapid fire” interviews that gets his audience updated on contemporary issues. This one on June 15, 2023, starts out with U.S. Representative Jerrold Nadler the 12th District of New York incredulously stating two year old should have worn masks because at the time there was no vaccine. My responses are short and evidence-based with citations. This is the type of interchange we should be seeing on main stream media with experts who should know the data cold have the alacrity to move quickly from topic to topic. Watch additional coverage on Rochelle Walensky, Demar Hamlin, Jamie Foxx, Kathy Huchul, and Propagandized “Misinformation.”
June 21, 2023
Posted by aletho |
Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science, Video | Covid-19, COVID-19 Vaccine, United States |
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Compassionate approaches for dealing with those who promote falsehoods and silence the truth
Peter Hotez is well-known for receiving millions for vaccine development and being a militant defender of the narrative who maliciously attacks anyone who challenges him but refuses to ever debate anyone who disagrees with him.
This became a big problem because prior to COVID-19 the media paraded him around to advocate for mass censorship of anyone who questioned vaccines. His publicity campaign then paved the way for the mass censorship we saw over the last few years (which likely cost millions of lives during the pandemic since everyone who questioned the dysfunctional pandemic response online was silenced).
After the initial objective was achieved, Peter Hotez pivoted to calling for the government to target and silence anyone who questioned the vaccine narrative. He justified these fascist demands with his lies that anyone who questioned the vaccines were mass murders and engaged in a war against science.
Recently, Hotez (who always hurls inflammatory allegations) picked a fight with Joe Rogan and the unprecedented public response exposed Hotez’s grift to the entire world. Many in turn assumed Hotez’s refusal to debate vaccine misinformation (in return for a massive donation being given to a charity of Hotez’s choice) meant all of Hotez’s claims about helping the poor were nothing more than a grift.
Because of the damage Hotez has done to the world, I’ve dug into his background and discovered many concerning things about his character, how he sees himself and his past conduct. One of the most concerning things is that he was one of the mad virologists who was complicit in the GoF research on the SARS coronavirus which led to the lab leak that gave us COVID-19. Even more unbelievable, at the same time he did this, he had a massive grant from the NIH to develop a SARS vaccine for a SARS lab leak, a vaccine he has since developed and brought to market.
This is all hard to believe, so I did my best to both cover just who Hotez is in detail here and provide helpful perspectives on how to we can compassionately but effectively deal with difficult people like Hotez.
Read it here.
June 20, 2023
Posted by aletho |
Corruption, Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | COVID-19 Vaccine |
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Also voted for the Climate Protection Act
Often, the narrative put forth suggests that the restrictions and mandates related to Covid-19 were enforced upon citizens by their governments. This viewpoint could seemingly imply that if left to the discretion of the masses, these lockdowns, social distancing protocols, and mandatory vaccinations might never have seen the light of day.
However, one nation stands as a testament against this theory – a control country allowing us to examine the public sentiment more closely – Switzerland.
Switzerland distinguished itself as one of the few nations globally that entrusted its citizens with the power to vote on measures concerning Covid-19. The first referendum took place in June 2021. It was a time when only approximately a third of the populace was vaccinated, yet the poll results exhibited a significant majority support for the Covid laws with a staggering 60.2% favouring them.
Not long afterwards, in November 2021, Switzerland’s second referendum took place. This vote was particularly contentious as it encompassed an array of substantial measures like stricter restrictions, comprehensive contact tracing, and the issuance of vaccination certificates. Despite the divisive nature of these policies, an even greater number of people endorsed them, with a 62% majority, which interestingly, was also the fourth-highest voter turnout in Swiss history, standing at 65.7%.
Surely, in 2023, the outcome would be different? Nobody is talking about Covid anymore. With the global narrative having largely moved on from Covid, would the Swiss people continue to support these laws?
Yes they would and no, in 2023 the outcome is no different. Yesterday, a rare third referendum was held. At the end of 2022, the Swiss parliament decided to extend some aspects of the Covid laws, including the vaccine certificates, until summer 2024. The reason given was that a dangerous new Covid variant may emerge and the authorities would have to react quickly. Due to the extension, opponents of the policies obtained enough signatures to force a new referendum.
Despite the ongoing contention, a significant majority of 61.9% voted in favour of these laws.
59% of voters also agreed to pass a climate change law which aims to reach net-zero greenhouse gas emissions by 2050. Opponents said the plan would drive up electricity use and prove too costly for consumers but authorities plan to incentivise households and businesses to be more climate-friendly.
It seems people never learn and Covid restrictions & vaccine passes could return tomorrow if a new health panic were to emerge.
June 19, 2023
Posted by aletho |
Civil Liberties, Malthusian Ideology, Phony Scarcity, Science and Pseudo-Science | Covid-19, COVID-19 Vaccine, Human rights, Switzerland |
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Kennedy vs. Hotez might be a narrative-changer.
In south Alabama we have an expression: “If you’re scared, say you’re scared.”
Well, Dr. Peter Hotez – one of the best-known vaccine advocates and defenders of all the Covid mitigation measures – is obviously scared to death. He just needs to come out and admit it.
What scares Dr. Hotez is an invitation for him (Hotez) to debate presidential candidate and contrarian Covid expert Robert Kennedy, Jr. on Joe Rogan’s ultra-popular podcast show.
Apparently, Hotez kept bad-mouthing “disinformation super-spreader” Kennedy and Rogan finally had enough.
Rogan offered to donate $100,000 to Hotez’s favorite charity if Hotez would just come on his show and, in a debate with no time-table, debate Kennedy on vaccine effectiveness, safety and all the other allegedly “settled” Covid science.
As I write, the debate invitation has gone viral on Twitter with plenty of other wealthy people (like Steve Kirsch) ponying up money to make the debate happen. At last look, Dr. Hotez could net $1.5 million for his favorite charity by simply talking to Kennedy and Rogan for two or so hours.
Talk about easy money.
Needless to say, Kennedy is game for a “cordial” debate and, needless to say, he doesn’t need to be bribed to participate. He’ll do it for free and pay his own expenses to show up in the studio.
Truth be told (there’s that word – “truth”) … Nobody is surprised that Dr. Hotez is running from a genuine debate on Covid topics. This is because no expert in America has participated in a genuine debate on Covid topics in 40 months.
Apparently, one new feature of our “New Normal” “scientific method” is that real debates are no longer necessary.
In fact, they are strongly discouraged, which is exactly why Facebook, Google, YouTube, the CDC, “Joe Biden’s” White House and the corporate press have been pushing for censorship on steroids for so long.
For those who haven’t picked up on this yet, censorship also precludes real debates.
Hotez and every “expert” and authority of his ilk has been saying for almost four years that people like Kennedy who are spreading “disinformation” and “misinformation” are potentially killing and harming massive numbers of people with their false Covid claims.
According to the experts, the claims made by Kennedy, Kirsch (and Bill Rice Jr.!) are ridiculous, preposterous, obviously false, easily discredited, etc.
Such claims are interesting as they suggest that any debate with a Covid skeptic would be a lay-up or gimme to win. Even a cave man could humiliate RFK, Jr. in a debate about real science.
So, if victory would be so easy – and if one can make a couple million for his favorite charity – why not do this?
Speaking for myself, I’m tired of acting like I’m obtuse when I’m not. We all know the answer: The Dr. Hotez’s of the world are scared to death of a real debate.
If this isn’t a giant “tell” about these frauds and charlatans nothing is.
Also, every one of them are pro-censorship.
Facebook has been censoring content left and right for three-plus years, but Hotez’s cabal of “influencers” are demanding that Congress and the White House make social media companies censor even more content/speech that they don’t like.
The entire justification for North Korea-style censorship is that the disinformation spreaders are harming people. Presumably, Hotez’s noble goal is to save lives and shut up all the “disinformation” spreaders.
Well, what would shut them up more than a pay-per-view prize fight between one of the leading advocates of the Status-Quo narrative and the best known Covid skeptic in the world?
Once Dr. Hotez wipes the floor with Kennedy, every other vaccine super spreader will crawl back into a cave and keep his mouth shut from here on out.
My side will be disgraced and humiliated … and every neutral person will now know this.
In one fell swoop, the “disinformation” movement will suffer a lethal blow. Millions of lives will be saved because, in the future, everyone will know that Dr. Peter Hotez and Dr. Anthony Fauci were exactly right with everything they said about Covid.
Not only will Kennedy lose this “science” debate, his hopes of pulling an upset and winning the White House will also go down the toilet.
Dr. Hotez would be THE hero to all the groups, companies and bureaucracies who are having nightmares about Kennedy beating their chosen candidate, “Joe Biden.”
Kennedy’s Children Health Defense non-profit, which has been growing by leaps and bounds, would wither up and die.
Everyone would know that not only did the Covid vaccines save millions of lives, they’d also know that the massive spike in autism cases in recent decades had nothing to do with vaccines and the flu vaccine – which is now being questioned by more and more Americans – would once again be perceived as a must-get annual shot.
Hotez could also put to bed the claim that his side is anti-free speech because they would be allowing Kennedy and Rogan to deploy their dad-blasted free speech in said “debate.”
“See, we are NOT censors and we do believe in free speech and genuine debates in our democracy,” Hotez could show the world in this debate.
For all these reasons, it would seem Dr. Hotez and his side would achieve a panoply of positive, life-saving results, with no down-side whatsoever.
The only downside might be if, Hotez, in fact got annihilated in this debate and every American who witnessed the event started questioning all the claims the experts had made in the last four years (or decades for that matter).
But this scenario can’t be a possibility because the science is so “settled” and Kennedy is such a “wacko” and conspiracy theorist that he would have no chance of prevailing in any debate … right?
Of course, we all know Dr. Hotez knows he’d get his ass whipped in any debate with Kennedy. Fauci knows this, The New York Times knows this, Bill Gates knows this, every commentator at MSNBC and CNN knows this.
“Whatever you do, do NOT debate Robert Kennedy on Covid topics!” they are all now screaming at Dr. Hotez.
If the debate is held, it will set Internet ratings records. The fact that Hotez is running from said debate is already giving another huge boost to the presidential campaign of RFK, Jr, who is having no trouble going around the MSM “gatekeepers of the news,” who all despise and fear him.
In fact, that’s another reason the debate can’t be allowed. It’s almost a given that RFK, Jr. would go off on the captured mainstream press in said debate.
Dr. Hotez would be the one defending the credibility of The New York Times and singing the praises of Big Pharma, which has of course always been as honest as the day is long.
If enough Americans keep calling Dr. Hotez a sissy, maybe this will goad the previously cocky doctor into taking the bait and actually debating Kennedy.
If so, this might qualify as a game-changer and give the world it’s very first honest discussion of Covid policies. It might also help elect a president who genuinely wants to dismantle the Military Industrial Complex and the Science/Medicine Industrial Complex.
But my bet is Dr. Hotez won’t debate.
There’s another expression we’ve all heard: “You can run, but you can’t hide.” Well, in our surreal New-Normal times, apparently the experts and authorities CAN run and they can hide. That’s what they’ve been doing for 40 months and, as far as I can tell, they are still in power. So that strategy is working perfectly.
June 18, 2023
Posted by aletho |
Deception, Progressive Hypocrite, Science and Pseudo-Science | Covid-19, COVID-19 Vaccine, United States |
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An analysis published earlier this month in Pediatrics concluded the COVID-19 mRNA vaccines are safe and effective in preschool-age children — a conclusion trumpeted by media outlets such as Parents and Medscape.
But the study, conducted by Kaiser Permanente researchers with funding from the Centers for Disease Control and Prevention (CDC), raises more questions than it answers.
Researchers followed children (mostly 4 years old or younger) who collectively received more than 245,000 doses of either the Pfizer or Moderna mRNA products and “found no indications of serious side effects,” according to a Kaiser Permanente news release.
Using a form of surveillance monitoring known as rapid cycle analysis, investigators performed weekly sequential analyses for 19 safety signals, including myocarditis, pericarditis, seizures, heart attack, Bell’s palsy, neurological inflammatory conditions, anaphylaxis and several others.
The study period was from June 2022 to March 2023.
Instead of using a comparable group of unvaccinated children as the control, the authors compared adverse events occurring 1-21 days after vaccination in one group, with outcomes among children in another group who had received the shot at some point between 22 and 42 days previously.
Time since inoculation was the only distinguishing feature, and the only factor that might account for inter-group differences.
The study, therefore, boils down to the question of whether children who received an mRNA shot about 10 days previously experienced more or fewer adverse events than children who received their jab about 32 days previously.
Data were mined from the Vaccine Safety Datalink (VSD), a repository of patient data from eight private healthcare systems, which included five Kaiser Permanente regions and three other large health entities.
Up to three doses of the Pfizer-BioNTech product were given to 135,000 children, ages 6 months to 5 years, while 112,000 children, ages 6 months to 6 years, got the Moderna gene therapy.
Subject demographics more or less reflected the populations served by these healthcare companies.
The authors wrote that their safety surveillance over nine months “did not detect a safety signal for any outcome during the 21 days after vaccination. Importantly, no cases of myocarditis or pericarditis occurred after vaccination.”
The accompanying press release framed the conclusion even more positively. According to corresponding author Dr. Nicola Klein:
“Parents can be assured that this large study found no serious side effects from the mRNA vaccines. … Parents can protect their young children from COVID-19 in the same way they vaccinate their children to protect from other serious childhood diseases.”
Perhaps anticipating the long list of questions regarding their work, the researchers discussed the potential limitations of their analysis, which they said included:
- Reduced statistical power, particularly for rare outcomes.
- Low vaccine uptake in the evaluated age group (“only” 24.7% of the eligible population received at least one shot).
- Surveillance did not include “all potential safety concerns.”
And the kicker:
“We may have underestimated or missed potential safety concerns if the biologically plausible risk interval for an outcome differed from our specified risk interval.”
Together, the choice of control group and the time period selected almost guaranteed “reduced statistical power,” particularly when comparing the two groups.
In a 2022 paper Klein noted reports from “worldwide” sources of myocarditis/pericarditis after mRNA COVID-19 treatments “especially among younger male persons [italics mine] 0 to 7 days after receiving dose 2.”
Although the incidence of heart inflammation was low in the 0-5 age group for the Pfizer product (14.4 per million doses, mostly after the second shot), the incidence of serious cardiac events rose markedly for older groups.
No data were available in the 2022 study for the Moderna shot.
For 18- to 29-year-old males — the youngest age group for which both Pfizer and Moderna data were available — Klein reported, based on VSD numbers, a cumulative myocarditis/pericarditis incidence of 135 cases per million for children who had received the two injections plus the booster.
For the Moderna product, the incidence was 185 per million. For females, the rates were about 10 per million for both mRNA shots.
Given the serious long-term consequences of heart inflammation, and its known occurrence among vaccinated teenagers and young adults, one wonders at the wisdom of giving mRNA shots to children who are even younger than those known to get sick from the treatments.
COVID-19 itself has been blamed for the rise in heart inflammation, but a search for data from very early in the pandemic, before this storyline emerged (possibly to hide the incidence of “vaccine” injuries), shows this to be a red herring.
A 2022 Italian study comparing myocarditis/pericarditis incidence pre- and post-COVID-19 reported that the annual incidence of myocarditis was significantly higher before the pandemic than during, with a rate of about 80 per million “pre” and 60 per million “during.”
The authors made a point to emphasize that “the incidence of myocarditis was significantly lower in COVID than in PRECOVID in the class of age 18-24 years” than for their general study population, which averaged 40 years of age.
The incidence of pericarditis was unchanged between the two time periods, at about 45 per million.
Comparing data from two far-flung studies should be undertaken with caution. However, the difference between a baseline of fewer than 60 cases per million for 18- to 24-year-old adults (the Italian study) and the 185 per million for “male persons” between 18 and 29 post-mRNA treatment (Klein et al.) clearly and inconveniently shatters the “safe and effective” narrative.
The lack of statistical power in Klein’s 2023 study, despite a very large “denominator” (total patients studied), is almost certainly due to the relatively small number of cases — which is exactly what one would expect when uncommon (but serious) side effects over such short time periods are compared.
True, this is an apples-to-apples comparison — but in this case, investigators pretty much used the exact same apples and reported their similarities as somehow noteworthy.
Klein’s data source(s) raise additional questions. Although the VSD is connected to the national Vaccine Adverse Event Reporting System (VAERS), how much of her raw data came from VAERS and how much came from VSD is unclear.
Eleven of VSD’s 13 participating commercial and academic hubs are “data reporting sites” whose contributions presumably include vaccine side effect reports.
The concern here is about motives and incentives. VAERS data are based mainly on self-reporting and are known to be gross underestimates of the actual number of incidents.
By contrast, hospitals and healthcare systems, e.g. those participating in VSD, were robustly incentivized to promote and administer the COVID-19 shots.
Along those lines, note that one author “received funding from Janssen Vaccines and Prevention for a study unrelated to coronavirus disease 2019 vaccines.” And lead investigator Klein “received grants from Pfizer for coronavirus disease 2019 vaccine clinical trials and from Merck, GSK, and Sanofi Pasteur for study work unrelated to the current study work.”
The rationale for immunizing children against COVID-19 has been hotly debated since the shots were first available to older adults in late 2020.
But by the time these treatments were authorized for children, it was already clear that kids do not get very sick from COVID-19 and are not a significant source of infection, either for the community or for “grandma” in her rocking chair at home.
As of early 2021, with the huge wave of Delta-variant fatalities in freefall, the number of U.S. pediatric COVID-19 deaths reported by the CDC was close to zero, both in terms of absolute cases and as a percentage of all deaths.
Yet in her interview with her institution’s media department, lead author Klein said:
“Even as the COVID-19 emergency has ended, we know that the coronavirus poses a long-term, serious threat to all ages, including children. Vaccinating children against COVID-19 benefits them by reducing the burden of illness, avoiding spreading the virus to family and others, and mitigating the small but real risk of serious illness.”
Angelo DePalma, Ph.D., is a contributing editor for The Defender.
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.
June 18, 2023
Posted by aletho |
Deception, Science and Pseudo-Science | CDC, COVID-19 Vaccine, United States |
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