False and Misleading Efficacy Claims — What is the Motivation?
Dr. Rochelle Walensky Tweeting Counterfactuals with Intent
By Peter A. McCullough, MD, MPH | Courageous Discourse | November 10, 2022
CDC Director, Rochelle Walensky, MD, MPH, for the record, continues to make false claims about the COVID-19 vaccine boosters with the apparent motivation of getting more Americans “fully vaccinated.” This is in the backdrop of an 8.4% rate of Americans over age 5 taking one of them.[i]
No matter how hard the internal pressure is at the CDC to get a “needle in every arm,” what would be such a strong motivation for Walensky to blatantly deceive Americans with such obvious counterfactual information?
She states “COVID-19 vaccines may not prevent every infection (as apparent in her personal case), but they do provide us important protection against severe illness, hospitalization, and death…”
In order for that claim to be valid by US regulations, a COVID-19 vaccine would need to reduce the risk of adjudicated COVID-19 hospitalization and death as a primary endpoint in a prospective, double blind, randomized, placebo-controlled trial. The benefit would need to be meaningful, e.g., ~20% relative risk reduction, and statistically significant, e.g., p<0.05. The conclusive study should have no significant threats to validity such as loss to follow-up. There has been no pivotal randomized trial, and no one can claim COVID-19 vaccines reduce hospitalization and death. The shortest section on the FDA Pfizer Fact Sheet is the “Benefits” section! This is given with the consent form and makes no claims about severity, hospitalization, and death.[ii]
She goes on to promote a two-month period between the last injection (presumably legacy mRNA) and the new bivalent vaccine. This schedule has never been tested and demonstrated to be safe in human beings. Even more shocking, the bivalent boosters which failed in animal studies to stop Omicron, have never been tested for safety or efficacy in human RCTs with clinical outcomes. In academic medicine and the pharmaceutical regulatory community, the question is WHY does Walensky cross the line into making false claims, an illegal act for fully FDA approved and marketed drugs/vaccines? Only senate or congressional hearings with direct questions will get the truth out of her.
Here are some possibilities: 1) she is following orders from higher governmental authorities, 2) she knows the claims are false but truly believes the only way for vaccination to work is to keep everyone vaccinated on a continuous basis no matter what the costs, 3) she is in a form of a trance or psychological state driven by fear in herself and for humanity where COVID-19 vaccination has become like a talisman with special powers and cannot be challenged. Indeed, Walensky has never comprehensively discussed safety of COVID-19 vaccination, and she has not disclosed who should NOT take a COVID-19 vaccine. So, the next time someone in your circles claims you or your loved one should take a COVID-19 vaccine to be “safe” or “protected” from serious outcomes, ask them to take a look at the consent fact sheet and read the tiny benefit section.
[i] CDC COVID Tracker, Accessed November 9, 2022
[ii] VACCINE INFORMATION FACT SHEET FOR RECIPIENTS AND CAREGIVERS ABOUT COMIRNATY (COVID-19 VACCINE, mRNA), THE PFIZER-BIONTECH COVID-19 VACCINE, AND THE PFIZER-BIONTECH COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5) TO PREVENT CORONAVIRUS DISEASE 2019 (COVID-19) FOR USE IN INDIVIDUALS 12 YEARS OF AGE AND OLDER, August 22, 2022
Feds Scramble To Hide Role Of Oath Keeper’s Informant In January 6th “Insurrection”
By Eric Striker | The Main Street Tribune | November 11, 2022
A bombshell New York Times report has revealed that Greg McWhirter, the Vice President of the Oath Keepers who helped lead the group’s presence on January 6th, is an FBI informant.
Federal officials worked hard to hide McWhirter’s status as a Confidential Human Source (CHS) in the seditious conspiracy trial of Oath Keeper’s leader Stewart Rhodes and his associates, presenting their asset in public filings as a mere “witness” instead.
In a furious November 8th filing, federal prosecutors accused defense attorneys of illegally disclosing confidential discovery about McWhirter to the press. It appears that the actual way McWhirter’s status was leaked was through a clerical error by DC court employees, who accidentally published the sealed document on the docket.
Federal officials have been suppressing information on the role their assets and agents played in inciting violence at the Capitol by having them testify as witnesses in cases related to January 6th.
McWhirter, a black Sheriff’s deputy in Montana, rose through the ranks of the Oath Keepers thanks in part to his existing contacts with law enforcement as well as his race. Rhodes regularly showcased McWhirter’s black heritage as evidence that he is not racist.
The infiltrator has also courted public controversy for other legally dubious stunts over the years. During the 2016 election, he called on members of his militia to patrol voting sites in order to discourage election fraud. In a more recent incident, he aided the FBI in attempting to manufacture an Oath Keeper’s conspiracy to kill members of Antifa in Portland as retaliation for the anarchist murder of Aaron Danielson.
Following the events of January 6th, McWhirter bought a gun shop and immediately began offering steep discounts on ammo and weapons to militia members, with implications that they had to prepare for civil war.
The defense for Rhodes, et al, was planning to call McWhirter as a witness in order to expose his role as an agitator. Yet, as the FBI informant boarded the plane to travel to his scheduled court appearance, he suffered heart trouble and could not testify. He is only 40-years-old.
On social media, many are speculating that federal agents either induced his emergency health issue with drugs or, more plausible, worked with him and his physician to fake the whole thing. In light of this curious coincidence, Rhodes’ defense was forced to rest its case without being able to cross examine the agent provocateur.
This is not the first irregular development in the trial. Witnesses Rhodes’ defense planned to call who were slated to tell the court that the defendants were innocent of plotting violence at the Capitol had FBI agents visit their homes right before they were scheduled to testify. The FBI agents told them that they would legally incriminate themselves and be prosecuted if they spoke in Rhodes’ defense. This intimidation tactic proved effective, leading to witnesses taking the fifth amendment when called, much to the shock and frustration of the defense.
McWhirter was not the only person working for the FBI inside the Oath Keepers. Another black member, Abdullah Rasheed, was also exposed in court for providing information on the group’s inner workings to federal agents in the run up to January 6th.
In addition to this, the FBI appears to be preparing to thwart expected Congressional inquiries into domestic counter-terrorism operations. Journalist Julie Kelly recently reported that Christopher Wray is rushing to replace the head of its Washington Field Office, Steven D’Antuono, who has led agents in using controversial tactics across the country to entrap persons with right-wing political beliefs of all types in fictitious terror plots. D’Antuono suddenly announced his retirement despite his recent lucrative and prestigious promotion, which will make it difficult for Congress to question him on his actions under the color of law in the last three years.
The Oath Keeper’s trial, which to date is the most serious and high profile prosecution of all January 6th cases, will soon be going to jury deliberation.
Pentagon exploits post 9/11 laws to wage ‘secret wars’ worldwide: Report
The Cradle | November 9, 2022
A report released last week by the New York University School of Law’s Brennan Center for Justice details how the US Department of Defense (DoD) has been allowed to covertly deploy troops and wage secret wars over the past two decades in dozens of countries across the globe.
Among the nations in West Asia affected by these so-called ‘security cooperation authorities’ are Lebanon, Iraq, Syria, and Yemen; however, they also include many African and Latin American nations.
Known as ‘security cooperation authorities,’ they were passed by the US Congress in the years following the 11 September attacks, and are a continuation of the 2001 Authorization for Use of Military Force (AUMF), a piece of legislation that has been stretched by four successive governments.
According to the report, the AUMF covers “a broad assortment of terrorist groups, the full list of which the executive branch long withheld from Congress and still withholds from the public.”
Following in this tradition, the ‘security cooperation authorities’ being abused by the Pentagon are Section 333 and Section 127e of Title 10 of the United States Code (USC).
Section 333 authorizes the US army to “train and equip foreign forces anywhere in the world,” while Section 127e authorizes the Pentagon to “provide support to foreign forces, paramilitaries, and private individuals who are in turn supporting US counterterrorism operations,” with a spending limit of $100,000,000 per fiscal year.
However, thanks to the vague definition of ‘support’ and ‘training’ in the text of these laws, both Section 333 and Section 127e programs have been abused to target “adversarial” groups under a strained interpretation of constitutional self-defense; they have also allowed the US army to develop and control proxy forces that fight on behalf of – and sometimes alongside – their own.
As a result of this, in dozens of countries, these programs have been used as a springboard for hostilities, with the Pentagon often declining to inform Congress or the US public about their secret operations under the reasoning that the incidents are “too minor to trigger statutory reporting requirements.”
“Researchers and reporters uncovered Section 127e programs not only in Afghanistan and Iraq, but also in Cameroon, Egypt, Kenya, Lebanon, Libya, Mali, Mauritania, Niger, Nigeria, Somalia, Syria, Tunisia, and Yemen,” the report highlights.
Researchers also point out that defense authorities “have given little indication of how [they] interpret Section 333 and 127e.”
Even more concerning, and ignoring the damage caused by these ‘anti-terror’ laws, the US Congress recently expanded the Pentagon’s security cooperation authorities, particularly with Section 1202 of the National Defense Authorization Act (NDAA).
Section 1202 allows the US army to allow “irregular warfare operations” against “rogue states” like Iran or North Korea, or “near-peers,” like Russia and China.
The report comes at a time when the US army and its proxy militias are accused of illegally occupying vast regions of Syria and Yemen, looting oil from the war-torn countries, just over a year after their brutal occupation of Afghanistan ended. Moreover, a former US official on Tuesday revealed that anti-Iran militias are being armed in the Iraqi Kurdistan Region (IKR), where both the CIA and the Mossad are known to operate.
Good News on Omicron Outcomes from Prison
Captive Environment Allows Real Look at Risk for Hospitalization and Death
By Peter A. McCullough, MD, MPH | Courageous Discourse | November 8, 2022
Prisoners and staff are a prototypical congregate group amenable to epidemiologic study and in the setting of the SARS-CoV-2 outbreak, ideal for study of the patterns of spread and risk for serious outcomes.
Throughout the pandemic, review and interpretation of peer-reviewed manuscripts in widely read journals has required careful review of data in supplementary tables. The conclusions by the authors in many papers must be ignored given the heavy bias for all journals to “promote” mass vaccination. For example, thus far, there has not been a single paper in the New England Journal of Medicine that has concluded COVID-19 vaccines are unsafe, or not indicated, or do not have a favorable risk to benefit ratio.
Prior to COVID-19 for any new therapy or surgery, there are always divergent views where some papers conclude an intervention is beneficial and others do not. Disagreement is normal in medicine. The pervasive heavy-handed government intelligence community and public health agency operations have biased the medical journals to publish a one-sided story on COVID-19 vaccination. The paper by Chin et al, in the New England Journal of Medicine is a perfect example.[i] They studied 59,794 residents and 16,572 staff, using data collected from December 24, 2021, through April 14, 2022. Buried in the supplemental tables are important data on the real risk of hospitalization and death with the Omicron variant in prisoners characterized by whether they had prior COVID-19 and how many doses of a vaccine they had received.
Chin ET, Leidner D, Lamson L, Lucas K, Studdert DM, Goldhaber-Fiebert JD, Andrews JR, Salomon JA. Protection against Omicron from Vaccination and Previous Infection in a Prison System. N Engl J Med. 2022 Oct 26. doi: 10.1056/NEJMoa2207082. Epub ahead of print. PMID: 36286260. Supplemental Tables.
As shown, there is a negligible risk of hospitalization and death with Omicron infection. Specifically, there were zero deaths in the unvaccinated. To demonstrate how far off-base authors and editors are on interpretation, take a look at the paper’s conclusions:
“Our findings in two high-risk populations suggest that mRNA vaccination and previous infection were effective against omicron infection, with lower estimates among those infected before the period of delta predominance. Three vaccine doses offered significantly more protection than two doses, including among previously infected persons.”
My conclusions are considering natural immunity status, COVID-19 vaccination provided no meaningful protection against hospitalization and death with Omicron. Based on these data, a rational prison physician or health administrator would conclude that bivalent boosters for Omicron are not clinically indicated nor medically necessary. So next time you see headlines regarding a journal article, look for a second opinion from “Courageous Discourse” or other reliable stacks and sources of analysis.
[i] Chin ET, Leidner D, Lamson L, Lucas K, Studdert DM, Goldhaber-Fiebert JD, Andrews JR, Salomon JA. Protection against Omicron from Vaccination and Previous Infection in a Prison System. N Engl J Med. 2022 Oct 26. doi: 10.1056/NEJMoa2207082. Epub ahead of print. PMID: 36286260.
STOP the Infanticide! 5,000% Increase in Fetal Deaths Following COVID-19 Vaccines!
The U.S. Government’s Vaccine Adverse Events Reporting System (VAERS) was updated today, and there are now 4,534 fetal deaths recorded in VAERS following COVID-19 vaccines given to pregnant and child-bearing women. (Source.)
And these recorded fetal deaths are but a fraction of the real number of unborn children who have died since the COVID-19 experimental vaccines were given emergency use authorization, as a previous report published for Department of Health and Human Services stated that fewer than 1% of all vaccine adverse events are actually reported to VAERS. (Source.)
Three of these fetal deaths have followed the new Bivalent COVID-19 booster shots from Pfizer and Moderna, including a 26-year-old woman from Arizona who developed breast cancer following the vaccine, and chose to have chemotherapy and terminate the life of her unborn child.
VAERS ID: 2447825: Began noting a breast lump 9/2021 Biopsied ER/PR + HER 2- breast cancer MRI 3/17/2022 with hepatic mets multiple small pulmonary mets also noted. Liver biopsy 4/1/22 consistent with metastatic breast cancer. Noted to be pregnant when she went for port-a-cath.
Choose to terminate pregnancy 3/31/22 to allow for complete chemo. ACT 4/5/22-7/23/22 . PET noted resolved axillary nodules and pulmonary nodules, Liver mets responding but still with activity. Sarted Lupron and anastrozole 8/10/22, Kisqoli addes 8/23/22.
I am not saying MRNA vaccines caused this but I have seen way more and way younger breast cancer in this remote population in than in a very long career.
We have had 18 new cancers since the vaccines only 1 was unvaccinated. This is the youngest ever. (Source.)
By way of contrast, for the 30 years prior to the emergency use authorization of the COVID-19 vaccines, there were 2,245 reported cases of fetal deaths following all FDA-approved vaccines, or about 75 fetal deaths per year. (Source.)
Taking the total fetal deaths following COVID-19 vaccines for the year 2021, 3,774 fetal deaths (source), that is an increase of 4,943% over the yearly average of fetal deaths following all FDA-approved vaccines for the previous 30 years.
Besides these government statistics from VAERS, medical professionals are corroborating this evidence of infanticide by COVID-19 vaccines based on the increase they are seeing in fetal deaths and stillborn babies following the roll outs of the COVID-19 vaccines.
An alleged leaked email from a “managing nurse” from a hospital in Fresno, California, states that there has been an increase in stillbirths following the COVID-19 vaccines, and that this trend is expected to continue according to Epoch Times.
This follows a report we recently published by Dr. John Campbell regarding the increase in neonatal deaths in Scotland.
And that follows another report we published last month (October, 2022) from Dr. James Thorp, a board certified OBGYN and Maternal Fetal Medicine Physician with over 43 years of obstetrical experience, who was interviewed by Dr. Drew Pensky and stated that in the past two years since the mRNA COVID vaccines were introduced, he has seen an “off-the-charts” rise in sudden fetal death and adverse pregnancy outcomes, such as fetal malformation and even fetal cardiac arrest, among his patients.
Pfizer to fast-track more vaccines for pregnant moms, despite mounting evidence rushed COVID shots harmed babies
The Defender | November 9, 2022
On Nov. 1, Pfizer issued a press release about an investigational vaccine for pregnant women the company said will protect babies from respiratory syncytial virus (RSV).
Not coincidentally, RSV is the latest viral bugaboo to hit the headlines, with frantic news accounts of “overwhelmed” hospitals sounding eerily reminiscent of the early coronavirus fear-mongering.
Buoyed by the successful global marketing of its COVID-19 jabs — an estimated 49% of pregnant women worldwide reportedly views the vaccines favorably and almost 1 in 4 pregnant women in the U.S. took them — Pfizer is hoping to hit another home run with the RSV vaccine.
The vaccine maker said it intends to seek U.S. Food and Drug Administration (FDA) approval by the end of the year.
The FDA, meanwhile, has been busy handing out “Breakthrough Therapy” designations to Pfizer as if they were papal dispensations, signaling a regulatory willingness to speed up approval not only for Pfizer’s RSV vaccine but also for a maternal Group B Streptococcus (GBS) vaccine the company is developing.
To this expedient end, the FDA allowed Pfizer to “stop the [RSV] study short,” halting enrollment at about 7,400 participants — though the trial was supposed to involve 10,000 pregnant women.
Researchers devoted to vaccine orthodoxy pay lip service to the need for an extra-high evidentiary bar for pregnancy vaccines — stating that such vaccines should not only prove they reduce illness, with minimal reactogenicity in the woman, the fetus and the neonate, but should also “demonstrate safety or lack of evidence of harm.”
However, those turn out to be empty words.
In fact, the influenza and Tdap (tetanus-diphtheria-acellular pertussis) vaccines that public health agencies have long recommended for pregnant women never underwent any clinical trial safety testing in that population, and the FDA never licensed those vaccines specifically for pregnant women.
Moreover, flu shots and Tdap shots have never even resulted in any statistically significant reduction in the outcomes they are supposed to address.
With the advent of Emergency Use Authorization COVID-19 vaccines, the FDA, Pfizer and other manufacturers barely made any pretense of assessing maternal safety, and likely “colluded together to conceal damaging data” about high rates of fetal death.
Other researchers, however — and even vaccine insiders — began to speak out in 2021.
For example, Canadian researchers writing in late 2021 worried that many of the systemic reactions commonly reported after COVID-19 vaccination might be “sufficient to affect fetal/neonatal development.”
Those authors included vaccinologist Byram Bridle, Ph.D., who earlier in 2021 characterized the COVID-19 vaccines’ disturbing biodistribution and accumulation in vital organs as “a big mistake,” and neurology professor Dr. Steven Pelech, who expressed repeated concerns about myocarditis and the vaccines’ risks to young people.
Now, as horrified pregnant women who took the COVID-19 jabs experience skyrocketing miscarriages, stillbirths and fetal malformations, they are wondering why regulators issued no warnings.
But as Pfizer’s exuberant RSV press release and the FDA’s complacent endorsement of clinical trial shortcuts suggest, vaccine makers and regulators not only intend to ignore or bulldoze even the most outsized safety signals but are clearly positioning themselves to go after pregnant women in an even bigger way.
‘Quibbles’ and questions
The details provided — or omitted — about Pfizer’s RSV clinical trial exemplify manufacturers’ and regulators’ cavalier approach toward pregnant women.
Commenting on Pfizer’s announcement, family physician Dr. Buzz Hollander — who clarified that he is predisposed to celebrate the new RSV vaccine offering — nonetheless noted a number of serious criticisms:
- Pfizer released “just a press release” but no data, making it “impossible to pick [the vaccine’s declared efficacy] apart.”
- Pfizer offered no explanation as to how it defined “severe” disease, its primary endpoint.
- A year into the trial, Pfizer fishily altered an important endpoint, defying a fundamental clinical trial design principle that “involves setting out in advance the endpoints that will be assessed.”
- In Hollander’s words, Pfizer “switched their secondary (critical!) endpoint of RSV hospitalizations to 360 days from 180 days… and then inspired my suspicion by not reporting any hospitalization data, interim or otherwise, in their breathless press release.”
- Researchers have published only one small safety study for the RSV shot, about which Hollander said: “I quibble with studies finding >40% of placebo participants reporting systemic symptoms; when queried enticingly enough, half of us might recall a headache or some fatigue the day after our placebo shot, and that can bury a difference in real adverse reactions compared to the vaccine group.”
- Curtailing study enrollment was unwise, Hollander said, because “bigger is better when it comes to … finding safety signals.”
- Earlier this year, GlaxoSmithKline (GSK) “stopped cold” a three-times-bigger trial of a similar RSV vaccine for pregnant women after detecting a safety signal, yet there has been no discussion as to why Pfizer’s maternal RSV vaccine is “fine” while GSK’s was deemed “untouchable.”
Hollander’s modest conclusion: “We should have all learned by now that even the appearance of cutting corners in the vaccine approval process will carry its own unknown costs.”
Readers reacting to Hollander’s post were less circumspect. One acerbically remarked, “The problem here is Pfizer. They’ve paid billions in fines for shady practices and data manipulation. And that was before the Covid vaccines (for which they’re indemnified).”
Another reader expressed his reservations even more succinctly: “Trust Pfizer numbers? You must be joking.”
Adverse pregnancy outcomes after COVID vaccination — no joke
As Pfizer, with the FDA’s help, tees itself up to “dominat[e] the maternal RSV vaccine market,” OB-GYNs on the front lines of maternal care are stepping forth to sound the alarm about the COVID-19 shots’ infanticidal fallout.
Dr. Kimberly Biss recently tweeted, “Since the vaccine rollout started, we have seen in our practice a decrease in new OB numbers, which would be infertility, by about 50%; we’ve also seen an increase in miscarriage rate by about 50%, and … probably about a 25% increase in abnormal pap smears as well as cervical malignancies.”
Similarly, Dr. James Thorp, in multiple interviews, described an “off-the-charts” rise in sudden fetal death and other adverse outcomes, including fetal malformation and fetal cardiac arrest.
Asked to comment on information recently leaked from a California hospital, Thorp characterized the uptick in fetal deaths — from under 6 per 1,000 in 2020 to more than 29 per 1,000 following the rollout of COVID-19 injections — as being “way way beyond” what the Centers for Disease Control and Prevention ordinarily would consider a safety signal.
Thorp published a preprint in September (along with co-authors who include Children’s Health Defense’s Megan Redshaw) describing “significantly more frequent” pregnancy-related adverse events reported to the Vaccine Adverse Event Reporting System, or VAERS, after COVID-19 shots than in the aftermath of flu shots — which themselves are far from benign.
Cataloging significant increases in “miscarriage, fetal chromosomal abnormalities, fetal malformation, fetal cystic hygroma, fetal cardiac disorders, fetal arrhythmia, fetal cardiac arrest, fetal vascular mal-perfusion, fetal growth abnormalities, fetal abnormal surveillance, fetal placental thrombosis, low amniotic fluid, and fetal death/stillbirth” and also menstrual abnormalities, Thorp and co-authors called for a “worldwide moratorium on the use of COVID-19 vaccines in pregnancy.”
For children who survive, Thorp suggested they may suffer from lifelong “vaccine-induced acquired immune deficiency syndrome.”
In Scotland, meanwhile, the government ordered an investigation into the “spike in newborn baby deaths” in 2021 and 2022, an increase “larger than expected from chance alone.”
Even in a gerrymandered study clearly designed to exonerate the COVID-19 shots during pregnancy — focusing on immediate reactions after a first or second dose and hampered by “limited perinatal outcome assessment” — researchers found that 4.4-7.5% of pregnant women reported obstetrical symptoms.
Careless and worse
As Substack writer Etana Hecht wrote last May, “The topic of pregnant and nursing moms getting vaccinated under encouragement and coercion is painful,” particularly once one becomes aware of “how carelessly the most precious among us are being treated.”
That carelessness is evident as we witness some of the same players involved in the COVID-19 vaccine fiasco now circling back around to help build the case for Pfizer’s RSV vaccine.
That includes figures such as Dr. Robert Frenck, the Pfizer-beholden principal investigator of the Cincinnati Children’s Hospital clinical trial that tested the company’s COVID-19 shot in children. Frenck reported 12-year-old Maddie de Garay’s serious vaccine injuries to the FDA as a mere “stomachache.”
Graphs clearly show that none of the vaccines pushed on pregnant women are safe for babies or moms — but given that from one-fourth to one-half of pregnant women acquiesce to getting them, those who know the truth need to work even harder to get the word out.
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.
Effects on mother and child that bear out Mike Yeadon’s warnings
By Neville Hodgkinson | TCW Defending Freedom | November 7, 2022
A British scientist with 32 years of experience in the pharmaceutical industry warned right at the start of the Covid vaccine rollout that under no circumstances should the gene-based, mRNA jab be given to women of child-bearing age without studies to confirm it was safe.
Dr Mike Yeadon, former vice president for research at Pfizer, one of the manufacturers of the experimental mRNA products, filed a petition with the European Medicines Agency on December, 1, 2020, urging that even testing the jab on human volunteers was unethical without significant safety concerns being taken into account.
One of these was a similarity between virus proteins targeted by the proposed vaccinations and a protein (syncitin) essential for forming the placenta in pregnancy. If antibodies produced by the jab also acted against those proteins, the petition said, ‘it would result in vaccinated women essentially becoming infertile’.
Co-signed by Dr Wolfgang Wodarg, a leading German physician, the document also warned that the vaccine trials were much too short to flag up late adverse effects. It added that the design was such that the trials could not show whether the product worked either in stopping a person from becoming infected, or from infecting others.
Subsequently, Yeadon became one of the first scientists to highlight evidence from a previously confidential Pfizer study showing that the vaccine products do not stay at the injection site but become widely distributed throughout the body, including the ovaries.
In view of the toxic nature of the ‘spike’ protein that the jab manufactures (summarised here), Yeadon warned in August, 2021: ‘My assumption at the moment is that these vaccines are concentrating in the ovaries of every female who has been given them. We don’t know what that will do, but it cannot be benign and it could be seriously harmful.’
It is now widely acknowledged that the jab neither protects against infection nor transmission, as Yeadon and Wodarg spelled out in their petition. If their knowledge had been sought at the outset of the Covid crisis the UK alone could have been spared the £500billion lockdown bill, with enormous associated social damage.
But what about the fertility warnings? Despite his years of experience at the top of his field, Yeadon has been vilified for speaking out. Is he really no more than ‘a hero of Covid conspiracy theorists’, as the Times described him?
Birth rates have fallen significantly in many countries, including the UK, in the wake of the vaccine rollouts. Various reasons for the fall have been suggested – usually excluding the jab.
Yet Dr James Thorp, a 68-year-old American physician who has practised obstetrics for more than 42 years and sees thousands of high-risk pregnant patients each year, has observed many complications attributable to the jabs, including foetal death and miscarriage. ‘What I’ve seen in the last two years is unprecedented,’ he says.
With help from several colleagues, he compared rates of adverse events following the Covid jabs with those reported post-flu vaccination in women of reproductive age. The focus was on events related to pregnancy and menstruation, using data from the US Vaccine Adverse Event Reporting System (VAERS).
A preprint of their findings published on September 28 shows a thousand-fold increase in menstrual abnormalities after the Covid jab, and significant increases in miscarriage, foetal malformation, growth abnormalities, cardiac disorders, foetal death and stillbirth.
Thorp has also highlighted risks to newborn babies taking milk from their vaccinated mothers. One study found mRNA from the jab in five out of 11 lactating women who had received the vaccination within six months of their delivery.
Last month, in a wide-ranging review in the US-based Epoch Times of these and other findings, US microbiologist and biomedical scientist Dr Sean Lin revealed that Thorp ‘has seen at least three newborns, completely healthy at the time of their birth, who passed away after being breastfed by their recently vaccinated mothers’. This suggested the vaccine components can not only accumulate in the ovaries but can also be passed on to infants via breastfeeding, he wrote.
He added that details of animal experiments performed before the jabs were authorised, recently obtained under freedom of information legislation, showed that mRNA and spike protein can travel through all barriers in a mother rat to enter its foetus. The rats themselves experienced toxicity during gestation, with some becoming infertile and losing the use of their hind legs.
Calling for an end to all Covid shots for pregnant women until long-term safety data become available, Lin writes: ‘The medical field and health agencies should still adhere to the fundamental ethical principle of ‘Do No Harms’.’
A hospital memo leaked to the Epoch Times by a nurse in Fresno, California, revealed how the hospital is experiencing a dramatic rise in the number of stillbirth cases, now upwards of 22 a month compared with an average of one to two every three months previously. This massive increase seems to align with similar evidence from across the country showing a potential rise in problems with fertility, miscarriages and foetal development, the newspaper reported.
Could the vaccine have contributed to a ‘very unusual’ spike in deaths among newborn babies now being investigated in Scotland?
In the UK, one and a half million Yellow Card reports of suspected adverse reactions to the vaccines include 821 miscarriages and 58,171 reproductive/breast disorders.
With tens of millions of doses administered, those numbers have still not persuaded regulators that there is a problem, although real-world adverse effects can be at least ten times higher than those reported. ‘Our advice remains that the Covid-19 vaccines are safe and effective during pregnancy and breastfeeding,’ the Medicines and Health products Regulatory Agency (MHRA) reaffirmed in September.
A review last month in the journal Vaccine declared that based on studies published so far ‘there is no scientific proof’ of any association between the jabs and impaired fertility in either men or women.
It depends on what is meant by ‘scientific proof’. If scientists do not ask the right questions, they can avoid receiving unwelcome answers. Those who drove the vaccine rollout are choosing not to see the thousands of reported disorders as related to the jabs, despite the record numbers, and clearly demonstrated mechanisms of harm.
It took a mathematician/businessman, for example, to point out evidence of a dose-response relationship between the jabs and infant deaths, with significantly more deaths reported when the higher-dose Moderna jab is used during pregnancy than with the Pfizer product.
Igor Chudov, who highlighted this phenomenon using US Centers for Disease Control (CDC) figures, says the Moderna product is associated with nearly twice as many neonatal deaths as the Pfizer vaccine, and 42 per cent more miscarriages.
In the light of these data, he asks: ‘How can Covid vaccine given during pregnancy be safe, and NOT affect infant deaths? How come nobody at the CDC asked this question? How come our media is silent on this?’
It is as though there are parallel universes: one occupied by those who can see no harm, and the other by doctors and scientists who insist a grave situation is staring us in the face.
The latter include three American medical whistle-blowers who found a 2021 rise of nearly 300 per cent in miscarriages among women serving in the US Army compared with the previous five years. There was no increase in 2020, when Covid arrived.
Doctors calling for a halt to Covid vaccination for pregnant women often meet abuse and censorship.
In October 2021, obstetrician and gynaecologist Dr Christiane Northrup told the Epoch Times: ‘Women are having bleedings. The doctors in our area are doing hysterectomies in young women, like 30-somethings. They said “Oh, it’s not unusual”. Let me tell you, as a board-certified gynaecologist, that’s very unusual. Women’s periods are messed up all over the place . . . I’ve had a huge Facebook group of thousands of women talking about this situation that was removed.’
What of Yeadon’s worry that an immune reaction to the spike protein might block pregnancy?
A small study from Singapore, in 15 women, reported that none had developed anti-syncitin antibodies after the jab, but Yeadon says the actual data showed a clear increase, arbitrarily ruled as insignificant by the researchers.
‘It looked like someone had tried to dismiss our concerns by testing for evidence of the particular problem we’d warned about. Unfortunately, all they did is to reinforce our concerns.
‘We’d envisioned the risk that, in responding to the synthetic piece of virus spike protein, women’s immune systems would also make an immune response to their own placental protein. That’s exactly what was reported in the pre-print paper.
‘Based on this concern alone, all these experimental products as a class should have been completely contraindicated in women younger than menopause.’
He insists that a series of toxicology issues meant ‘adverse impacts on conception and ability to sustain a pregnancy were foreseeable from the start . . . There was and still is no data package supporting safety in pregnancy, or prior to conception.’
A Tale of Two Reporters in Moscow
Malcolm Muggeridge, Walter Duranty, and the collision of ideology with evidence
Malcolm Muggeridge, Moscow correspondent for the Manchester Guardian
By John Leake | Courageous Discourse | November 7, 2022
Blinded by Ideology: Part 4 in a series on Willful Blindness
Malcolm Muggeridge was an exceptionally talented journalist who lived in Moscow in 1933, working for the Manchester Guardian. Though attracted to communism in his youth, the experience of being in Stalin’s Russia and observing what was going on in it caused him to become disillusioned. Especially disturbing was his realization that Stalin’s army and police were—as part of their collectivization program—starving millions of landowning peasants (known as kulaks) in the Ukraine by confiscating their grain. This massive organized crime—known as the Holodomor—resulted in the deaths of millions in the winter of 1933.
Muggeridge was the only western journalist to report what was going on. When his reports were published, many of his fellow writers—including George Bernard Shaw, Aldous Huxley, Jean-Paul Sartre, Upton Sinclair and Theodore Dreiser, and Sidney and Beatrice Webb—refused to believe them and passionately asserted that Muggeridge was spreading falsehoods about Stalin’s regime. Muggeridge was related to the Webbs by marriage, and years later he told a funny story about Beatrice.
I remember Mrs. Webb, who after all was a very cultivated upper-class liberal-minded person, an early member of the Fabian Society and so on, saying to me, ‘Yes, it’s true, people disappear in Russia.’ She said it with such great satisfaction that I couldn’t help thinking that there were a lot of people in England whose disappearance she would have liked to organize.”
For decades, Muggeridge’s accurate reporting of the Holodomor was denied and suppressed. The dominant narrative of Stalin’s Russia in the early thirties was that propagated by the New York Times Moscow bureau chief, Walter Duranty, who vehemently denied the Holodomor. While Muggeridge’s true and courageous reporting was denied, Duranty won a Pulitzer Price for his concealment of one of the greatest crimes of the 20th Century. It’s a testament to the power of Duranty’s mendacious work that most Americans have still never heard of the Holodomor.
Walter Duranty, Moscow bureau chief for the New York Times
Over the last two years I’ve often thought about Muggeridge and Duranty as I have watched courageous scholars like Dr. Peter McCullough persecuted and censored, while COVID-19 vaccine ideologues are rewarded. Most notable is the COVID-19 vaccine propagandist, Dr. Peter Hotez, who was recently nominated for the Nobel Prize.
One of the most bizarre features of our bizarre time is that an experimental, gene transfer technology has become an object of unshakable devotion. Among members of the COVID-19 Vaccine Cult, belief in the substance (about which they know nothing) is an article of faith.
In the 1930s, 40s, and even 50s, many of the most prominent journalists, writers, intellectuals, and artists believed in Stalin’s Cult of Personality. Muggeridge knew (from his own observations) that they weren’t seeing the reality of Stalin’s regime. Because they viewed the world through the highly distorting lens of ideology, they couldn’t see what was right in front of them.
Why Does the UKHSA Vaccine Surveillance Report Never Mention Side-Effects?
BY AMANUENSIS | THE DAILY SCEPTIC | NOVEMBER 3, 2022
In the past few months I’ve read newspaper articles warning of the increased risk of death following gardening, stress at work, solar flares, sleeping in front of the television, hot weather, cold weather, shock of high energy bills, the price of food, laughing too much and sleeping in the wrong position – these recent warnings add to the multitude of stories on the health consequences of our dietary choices, sedentary lifestyle and climate change. If that wasn’t scary enough, we’ve also seen efforts to educate the public about how common sudden deaths are in younger adults and teenagers. Given this background of suddenly emerging risks to life resulting from our modern lifestyle, it is clearly very important to fully understand all risks that might be emerging resulting from the Covid vaccines, no matter how trivial.
With the above in mind, it is perhaps rather surprising that the Vaccine Surveillance Report from the UKHSA has never actually mentioned vaccine side-effects or complications. Sure, the word ‘safe’ is typically used a few times in each report, but there’s never been a mention of side-effects and their rates. They don’t even like to use the term ‘rare side-effects’ – as far as the Vaccine Surveillance Reports are concerned the vaccines are simply ‘safe’. They’ve never reported any of the data from the Yellow Card side-effect reporting system, nor mentioned any of the increasing numbers of scientific studies reporting on an increasing number of ‘complications’ after receiving the various vaccines.
I suppose at this point I could stop – since side-effects aren’t covered in the Vaccine Surveillance Reports, and this is a series of posts reviewing the UKHSA Vaccine Surveillance Reports, there’s nothing to discuss. However, vaccine side-effects and complications are important, so I hope that I can be forgiven for exploring this aspect of the vaccines a little further in this post.
Over the past 18 months there have been many studies which have found worrying high side-effect rates following vaccination. The results of these studies have been discussed in multiple places across the internet, and many of these studies have been covered by the Daily Sceptic. The only common theme has been the remarkable insistence by authorities worldwide on ignoring the results of these studies, except where the evidence has become overwhelming and they are forced into some response.
The vast array of side-effects found by these investigative studies is now too voluminous to cover completely here, so instead I’ll focus on a few specific side-effects and discuss the response to these new findings.
Thrombocytopenia and blood-clotting related problems
The first inkling that there might be a risk of thrombocytopenia (low blood platelet count) after vaccination came in January 2021, a mere month after the vaccinations started, after a doctor in New York died of complications following acute thrombocytopenia about two weeks after being given the Pfizer vaccine. Pfizer responded with a statement that this definitely wasn’t anything to do with their vaccine, despite acute thrombocytopenia being relatively rare and the doctor not being in a risk group. In the months that followed, many more cases of thrombocytopenia and other blood clotting disorders occurred, from Pfizer and the other vaccine offerings, but the official response remained coincidence. Eventually the volume of problems became too large to ignore, and in June 2021 the U.K. authorities decided that those aged under 40 shouldn’t be offered the AstraZeneca vaccine. I found this restriction to the AstraZeneca vaccine a bit odd, as the other vaccines appeared to have similarly high rates of clotting problems in the weeks following vaccination, but it appears that the authorities had chosen their demon to blame. Of course, older adults weren’t too keen to be told that they were going to have to take these risks, and demand for the AstraZeneca vaccine plummeted. A few months later the AstraZeneca vaccine was only made available to those who were unable to take the Pfizer vaccine (the only alternative in the U.K. at that time). Even though the known problems of clotting related disorders post-vaccination are bad enough, it isn’t clear if the instances of severe clotting related problems (resulting in hospitalisation) are also accompanied by higher numbers of clotting problems below the clinical threshold (‘microclotting’), or whether these mild cases might have longer term consequences. Another area of post-vaccine effects that demands more research.
Myocarditis
The risk from myocarditis first appeared in a leaked report out of Israel in April 2021 suggesting worryingly high rates occurring in younger males. Quite why it was deemed necessary for this safety-related information to be kept secret isn’t clear, but authorities worldwide responded quickly once the information was leaked to reassure everyone that this risk was very very low and that the vaccines were very very safe (and effective, of course). While the official line is that post-vaccination myocarditis is rare, studies keep on finding higher and higher incidence rates, particularly in the young male risk group. Indeed, in August a scientific paper describing the impact of Covid vaccination in Thailand suggested that the conditions suggestive of myocarditis and pericarditis after vaccination were found in over 29% of vaccine recipients aged between 13 and 18 years of age, and a similar result has since been described after vaccination in Switzerland. The longer term impact of these ‘mild problems related to the heart’ aren’t yet known.
Period related problems
All clinical studies into side-effects are mindful of the need to treat any issues related to sexual function carefully – individuals are less likely to seek medical attention when it comes to sex-related problems and those related to our reproductive systems in general. Thus it should have been a huge red-flag when anecdotal reports of heavy or missed periods following vaccination started to appear early in 2021. Alas, our authorities simply responded with the usual ‘it definitely isn’t the vaccines’ and ignored the problem. The complex situation regarding reporting of side-effects related to reproductive function is nicely illustrated by the number of problems reported to the Yellow Card side-effect reporting system – early May 2021 saw a huge increase in reporting of side-effects related to menstruation. The reason? Most likely, an article on the problem on BBC Radio 4’s Women’s Hour in late March, in which listeners were urged to report any problems into the Yellow-Card system. It is very disappointing that our side-effect reporting system could be so heavily influenced by a radio programme in this way. Really there should have been active monitoring of post-vaccination complications and side-effects, but the inadequate Yellow Card system is all we had. Official guidelines now state that problems related to menstruation are relatively rare but even if they do occur they’ll be of no consequence whatsoever and women shouldn’t worry about taking the vaccines. Eventually we’ll find out if this reassurance was correct.
What’s also troubling is the way that the only side-effects that are discussed in the traditional media are the ones that have been officially recognised (albeit under duress). What about the increase in hospital consultant activity for stroke victims over the last 18 months?
Or the increase in consultant activity for hormonal problems?
Or the increase in referrals for suspected cancers?
Like the significant increase in excess deaths that we’ve seen this year, there seems to be much going on but little interest on the part of our authorities to investigate these issues at all. Maybe they’re all the result of the lockdowns, maybe they’re due to Covid itself, maybe it was the vaccines, and perhaps it is all just a massive coincidence – but it simply isn’t good enough to decide that it can’t possibly be the vaccines and refuse to even discuss undertaking the research that might clarify the situation.
At least in recent weeks we’ve had an increase in calls for some robust investigations to be undertaken, such as discussed in the Daily Sceptic in mid October. Then again, we’ve also had the brief hour-and-a-half spent a week ago by the House of Commons to debate the issues around vaccine safety. Despite some MPs detailing concerns about the safety of the vaccines, the Chair was quick to respond with empty reassurances and the debate ended with a statement urging people to get vaccinated to protect themselves, others and the NHS. I fear that there’ll be quite some way to go before the full impact of the vaccines is accepted by our authorities.
An important aspect of the rate of side-effects and complications is the impact on the risk-benefit analysis used by our authorities to determine who should take the vaccines. The risk of side-effects should be tolerable so long as the benefit offered by any medical product is greater than the risks. Since the vaccines were introduced back in December 2020 we have seen marked changes both in the risks posed by the vaccines (more side-effects and complications have come to light) and the benefits offered (the vaccines clearly offer little protection against infection, their protection against hospitalisation and death appears to be rather less than claimed, and at the same time Covid appears to have evolved to become much less virulent). In addition, nearly everyone in the Western world will now have had a Covid infection, resulting in at least some natural immunity. Unfortunately, our authorities have never actually published any of their risk-benefit analyses and how the ratio changes with age and morbidity, so we can’t tell how new information on risks and benefits has changed the calculation. Then again, I suppose it is easier to be inconsistent if you never actually tell anyone what factors your decisions are based upon.
One of the big problems regarding the Covid mRNA vaccines in particular is that there were only sparse data published on how long the mRNA would remain active in the body and where it would end up (pharmacokinetics and biodistribution). Originally the reassuring voices told us that the mRNA would break down within hours, and that the mRNA vesicles would remain close to the point of injection. However, evidence has emerged in the months since our authorities proceeded to inject everyone in the world that has suggested that the mRNA remains active for many weeks following vaccination, that it travels to multiple organs in the body and that the pharmaceutical companies knew this prior to the vaccines being released. Even worse, a recent study has suggested that the mRNA is present in breast milk for a short time following vaccination (for fairness I must point out that our authorities still think that it is completely and utterly safe for recently vaccinated mothers to continue breastfeeding). I find it concerning that we’re only now starting to find out the full complexity of the interaction of the mRNA vaccines with the body.
Recent studies have estimated the current rate of serious short-term side-effects after the Covid vaccines at around one in 800. I find this number interesting, as I suspect that this is as bad a side-effect rate as could be found for a supposedly benign or prophylactic treatment. I estimate that an incidence rate of around one in 1,000 marks the point at which problems become apparent even to a casual observer, provided sufficient numbers are given the medical product. If a side-effect rate for a benign or prophylactic treatment is worse than this people would notice and demand that the medicine or medical treatment is withdrawn. Thankfully, there aren’t too many examples of terrible medical mistakes – probably the most famous example is Thalidomide, where around one in 1,000 mothers who took the drug gave birth to a child with serious physical malformations. Even so, it took three years before the nature of the problem was understood and Thalidomide was withdrawn from sale. It is perhaps interesting to note that at least in the early stages of the problem being recognised the blame was put on the nuclear tests that had occurred in previous years – was this the 1950s equivalent of ‘climate change’?
Where serious side-effects are more common than this for a supposedly benign product, the response is typically more rapid. The famous example here is Elixir Sulphanilamide, a treatment for bacterial infections created in the 1930s that caused over 100 deaths in the few weeks that it was for sale. The problem with Elixir Sulphanilamide was that it hadn’t been tested before release and the manufacturers hadn’t realised that a primary component was highly toxic. The owner of the company that made the elixir famously denied responsibility, stating that “we have been supplying a legitimate professional demand and not once could have foreseen the unlooked for results”. It was this scandal that led to the creation of the FDA in the USA, along with stringent requirements for the testing of new medical products. After the disaster it was demanded that never again would a medical treatment be released and given to many thousands of people without being fully tested to explore all potential problems (and not simply the ‘looked-for’ problems). As a side note, the outcome of the Elixir Sulphanilamide scandal was that the scientist who developed the formula committed suicide as a result of the extreme guilt of causing so much harm, while the company that released the medicine without testing was given a nominal fine. The manufacturer went on to produce further drugs (and profits) and after a succession of takeovers is now part of the pharmaceutical giant GlaxoSmithKline. Funny how it all works.
Next time I’ll discuss one of the most wildly enthusiastic aspects of the Vaccine Surveillance Report – the predictions made by computer-models of the reduction in infections, hospitalisations and deaths offered by the vaccines.
Amanuensis is an ex-academic and senior Government scientist. He blogs at Bartram’s Folly.
Jen Psaki says censorship deposition would be “burdensome” for her family life and new MSNBC gig
By Dan Frieth | Reclaim The Net | November 6, 2022
Jen Psaki, the former White House press secretary, and Department of Justice (DOJ) are fighting a subpoena requiring her to testify in the lawsuit filed by Missouri and Louisiana attorneys general – alleging that the Biden administration colluded with social media platforms to censor certain viewpoints on the pandemic.
The motion to quash the subpoena was filed in a federal court in Virginia. It argues that the deposition would be “extremely burdensome” for Psaki, who is preparing to be the host of a new show on MSNBC.
We obtained a copy of the motion for you here.
“Among other things, I understand that I would need to devote several days preparing for the deposition, as well as attending the deposition itself, and that would be highly disruptive to both my work and my family,” Psaki wrote in the request.
Psaki has in the past admitted that the Biden administration was flagging people’s speech to social media platforms.
The DOJ argued that Psaki’s deposition would result in a debate over executive privilege considering she was a top adviser to President Joe Biden.
The DOJ lawyer said: “If permitted to proceed, the deposition of Ms. Psaki would inevitably set the Executive and Judicial Branches ‘on a collision course’ through adjudications of executive privilege, thrusting the court into ‘the awkward position of evaluating the Executive’s claims of confidentiality and autonomy,’ and ‘difficult questions of separation of powers and checks and balances’ would quickly be pushed to the fore.”
“Plaintiffs have not identified any evidence showing or even suggesting that Ms. Psaki ever communicated with any social-media company in her capacity as Press Secretary about misinformation, much less that she ‘exercised coercive power’ to compel a social-media company to take any action,” the DOJ added.
Other defendants that have tried to use a similar “burdensome” defense have already been shut down by District Judge Terry Doughty who said, “The Court finds that both the public interest and the interest of the other parties in preserving free speech significantly outweighs the inconvenience the three deponents will have in preparing for and giving their depositions.”
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From the Archives
Why Saudi Ties to 9/11 Mean U.S. Ties to 9/11
By Kevin Ryan | Dig Within | September 27, 2015
Media interest in Saudi Arabian connections to the crimes of 9/11 has centered on calls for the release of the 28 missing pages from the Joint Congressional Inquiry’s report. However, those calls focus on the question of hijacker financing and omit the most interesting links between the 9/11 attacks and Saudi Arabia—links that implicate powerful people in the United States. Here are twenty examples. … continue
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