Peter Hotez’s War Against Science
Compassionate approaches for dealing with those who promote falsehoods and silence the truth
A Midwestern Doctor | June 18, 2023
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.
Switzerland Votes to Keep Covid Laws & Vaccine Passes
Also voted for the Climate Protection Act
NAKEDEMPEROR | JUNE 19, 2023
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.
The Great Debate that won’t happen
Kennedy vs. Hotez might be a narrative-changer.
BY BILL RICE, JR. | JUNE 18, 2023
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.
What’s Wrong With This Study? CDC Finds COVID Shots ‘Safe and Effective’ for Kids Under 4
By Angelo DePalma, Ph.D. | The Defender | June 16, 2023
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.
Confidential Pfizer document shows the company observed 1.6 million adverse events covering nearly every organ system
By Daniel Horowitz | conservative review |June 14, 2023
Over 10,000 categories of nearly 1.6 million adverse events – many of them serious and debilitating – brought to you by Pfizer!
You might not have heard it in the news, but in recent months, Pfizer’s pharmacovigilance documents requested by the European Union’s drug regulator, the European Medicines Agency, have been released. They show that Pfizer knew about a sickening level of injury early on. An August 2022 document shows that the company already had observed the following scope of vaccine injury:
- 508,351 individual case reports of adverse events containing 1,597,673 events;
- One-third of the AEs were classified as serious, well above the standard for safety signals usually pegged at 15%;
- Women reported AEs at three times the rate of men;
- 60% of cases were reported with either “outcome unknown” or “not recovered,” so many of the injuries were not transient;
Highest number of cases occurred in the 31-50 year age group, and 92% did not have any comorbidities, which makes it very likely it was the vaccine causing such widespread, sudden injury.
These numbers alone suggest that all COVID shots should be defunded and Congress must immediately remove liability protections from the manufacturers. But a more recent document released by the Europeans is even more devastating, because it breaks down the 1.6 million adverse events observed by Pfizer by category and subcategory of ailment and injury.
The 393-page confidential Pfizer document, dated Aug. 19, 2022, shows that Pfizer observed over 10,000 categories of diagnosis, many of them very severe and very rare. For example:
- Pfizer was aware of 73,542 cases of 264 categories of vascular disorders from the shots. Many of them are rare conditions.
- There were hundreds of categories of nervous system disorders, totaling 696,508 cases.
- There were 61,518 AEs from well over 100 categories of eye disorders, which is unusual for a vaccine injury.
- Likewise, there were over 47,000 ear disorders, including almost 16,000 cases of tinnitus, which even Mayo Clinic researchers observed as a common but often devastating side effect early on.
- There were roughly 225,000 cases of skin and tissue disorders.
- There were roughly 190,000 cases of respiratory disorders.
- Disturbingly, there were over 178,000 cases of reproductive or breast disorders, including disorders you wouldn’t expect, such as 506 cases of erectile dysfunction in men.
- Very disturbingly, there were over 77,000 psychiatric disorders observed following the shots, lending credence to Dr. Peter McCullough’s research observing case studies showing psychosis correlating with vaccination.
- 3,711 cases of tumors – benign and malignant
- Of course, there were 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 over 100,000 blood and lymphatic disorders, for both of which there’s a wealth of literature linking them to the spike protein.
When reading what Pfizer knew early on juxtaposed to independent studies, it’s clear that nobody could have mistaken most of these AEs for mere incidental ailments. Here is a list of 3,129 case studies chronicling vaccine injury in every organ system observed in this Pfizer document.
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. One of the infamous cases of vaccine injury was Maddie de Garay, an Ohio teen who became disabled for life immediately after participating in the Pfizer clinical trial. Her story is chronicled in chapter 16 of my book. I checked this confidential document and found that they knew of 68 cases of her rare diagnosis, chronic inflammatory demyelinating polyneuropathy.
The broad scope of injuries affecting every single organ system is simply extraordinary. Yet to this day, the FDA continues to criminally label the Pfizer shot as safe and effective. To this day, the label indicates the shot is a fully protective vaccine and also fails to mention all of these side effects, as required by law.
Recently, Peter Doshi, editor of the British Medical Journal, wrote a letter to the FDA requesting that the agency update its labeling to reflect the reality of what we’ve learned about the shots. Specifically, he asked that they include the following side effects on the label: multisystem inflammatory syndrome in children, pulmonary embolism, sudden cardiac death, neuropathic and autonomic disorders, decreased sperm concentration, heavy menstrual bleeding, and detection of vaccine mRNA in breast milk. The causal relationship of all these AEs to the vaccine is backed by substantial research, surveys, and adverse event reporting systems.
Unfortunately, the FDA denied the causal relationship between any of these side effects and the COVID shots. Even with regard to the request that officials clarify on the label that the shots don’t stop transmission, the FDA replied, “We are not convinced that there is any widespread misconception about this.”
“Product labeling should be informative and accurate, not promotional. The law requires it, and following the law shouldn’t be optional,” bemoaned Doshi and the other authors in a piece at TheHill.
The question is whether Republicans in the House will force the FDA to comply with the law by using the leverage of the appropriations bills for the FDA and HHS. So far, there has been no reckoning for their false marketing and the devastating human toll it has cost. Oh, and that is just the short-term human toll.
Secret Pfizer Document Shows Company Observed 1.6 Million Injuries Following COVID Vaccination
BY MEGAN REDSHAW | JUNE 15, 2023
A recently released Pfizer document shows the pharmaceutical giant in August 2022 was aware of 1.6 million adverse events reported by those who had received its COVID vaccine.
The adverse events spanned more than 10,000 different categories and affected nearly every organ system in the body. Yet, Pfizer still concluded its shot was safe and effective.
According to Pfizer’s 396-page “confidential” pharmacovigilance document obtained by the European Medicines Agency, the company observed 508,351 case reports containing 1,597,673 adverse events. One-third of all adverse events were classified as “serious” — a number well beyond the 15% threshold that should trigger a safety signal.
The document shows that adverse events were three times more common in women than men, with 60% of all reports classified as “not recovered” or outcome unknown. The highest number of cases affected the 31-50 year age group.
Because 92% of individuals did not have a comorbidity, it’s unlikely their adverse events could be attributed to anything but Pfizer’s COVID-19 vaccine.
The document further categorized the 1.6 million adverse events observed by Pfizer into categories and subcategories based on injury. According to journalist Daniel Horowitz, Pfizer observed more than 10,000 categories of diagnosis, many of which were severe or rare.
For example, 73,542 cases in 264 categories of vascular disorders were reported by individuals after receiving Pfizer’s COVID vaccine, 696,508 cases of nervous system disorders were reported, and 61,518 reported eye disorders in 100 different categories.
More than 47,000 ear disorders were reported, including 16,000 cases of tinnitus, 225,000 reports of skin and tissue disorders, 190,000 respiratory disorders, and more than 178,000 reproductive and breast disorders.
There were 77,000 reports of psychiatric disorders reported following vaccination, 3,711 cases of tumors, more than 100,000 reports of lymphatic disorders, and 127,000 reports of cardiac disorders in more than 270 categories.
The document also shows Pfizer was aware of 68 cases of chronic inflammatory demyelinating polyneuropathy — the rare and severe neurological disorder experienced by Maddie De Garay during Pfizer’s clinical trials that left her confined to a wheelchair.
At the end of hundreds of pages of observed injuries, Pfizer concluded the risks of its COVID-19 vaccine “evaluated in the context of the benefits” showed the shot had a favorable benefit-risk profile.
“No additional changes to the BNT l 62b2 RSI or additional risk minimisation activities in addition to those in place are warranted at this time,” the company, which made billions off its COVID vaccine, wrote.
To date, the U.S. Food and Drug Administration has not updated the product label for Pfizer’s COVID vaccine to include a list of its potential adverse events, nor has Pfizer been held accountable for failing to disclose these potential vaccine injuries to the public.
HHS is Still Wasting Money Fighting Online Covid “Disinformation”
By Dan Frieth | Reclaim The Net | June 17, 2023
Apparently, Covid discussions are still a thing worth cracking down on. That’s at least according to The Biden administration, which is injecting $500,000 into Texas Woman’s University as part of a grant program aimed at curbing COVID-19 “misinformation” and “disinformation” allegedly aimed at Hispanics, according to funding records reviewed by the Washington Examiner. The grant aims “to expand research on mitigating the effect of misinformation and disinformation” regarding “COVID-19 prevention and treatment initiatives among Hispanics.”
Timeline: Kicking off on May 10 and set to wrap up in April 2024, this grant is part of the Department of Health and Human Services (HHS)’s Food and Drug Administration’s portfolio. It’s part of Biden’s broader push to censor alleged disinformation by joining forces with social media platforms on content moderation – a move likened to “censorship” by some Republicans.
What GOP says: This funding allocation may prod GOP lawmakers to probe deeper into the Biden administration’s methods in countering certain types of speech. House Republicans, according to the Washington Examiner, are considering wielding the appropriations process as a tool to block federal agencies from pumping money into domestic initiatives tagged as combating “disinformation.”
What HHS did before: In 2021, HHS, spearheaded by Secretary Xavier Becerra, allegedly dabbled in misinformation tracking, by offering guidance to Twitter and Facebook on handling virus-related content. The US Surgeon General Vivek Murthy admitted in an August 2021 call with education groups, that the government was “working to combat misinformation in many ways, one being working with tech companies.”
Skeptical voices: Brian Harrison, a former HHS chief of staff under Trump and a current GOP Texas state House member, communicated his skepticism to the Washington Examiner: “I have no confidence this is anything more than Biden’s HHS spending money we don’t have on government censorship efforts.”
Inside the project: Texas Woman’s University’s venture consists of crafting a “social network analysis” to scrutinize “misinformation consumed by the Hispanic community.” It involves conducting focus groups, creating “an economic impact analysis of proposed informational strategies for Hispanics,” and establishing a “longitudinal misinformation/disinformation index.” The study, set in El Paso, Texas, is also sifting through social media content in both English and Spanish.
Deja vu?: The aforementioned “index” has set off alarm bells due to its echo of a tool from the State Department’s Global Engagement Center, which previously backed the Global Disinformation Index, a British entity that faced criticism for supposedly operating blacklists of conservative media outlets.
HHS’s stance: In response, HHS spokeswoman Anne Feldman said: “HHS does not censor speech.”
Roles of Bromelain and Curcumin in Battling Recurrent SARS-CoV-2 Spike Protein Exposures
Natural Products have Strong Rationale for Use Post-COVID-19 and Vaccine Syndromes
By Peter A. McCullough, MD, MPH | Courageous Discourse | June 16, 2023
I find it interesting that a large group of post-COVID-19 acute sequalae are occurring in those who have taken failed COVID-19 vaccines. We are a long way off from definitive clinical trials of multidrug strategies for patients who have had multiple exposures to the SARS-CoV-2 Spike protein via vaccination or recurrent COVID-19.
Kritis et al point out:
“Curcumin (diferuloylmethane) is a natural phenol found in turmeric (Curcuma longa), a member of the ginger family of plants [4]. Curcumin modulates inflammation preventing the subsequent cytokine storm by inhibiting multiple transcription factors such as nuclear factor kappa B (NF-kB) and signal transducer and activator of transcription 3 (STAT-3), and downregulating the proinflammatory cytokines, as this has been demonstrated in human macrophages after influenza virus infection [4,6]. Additionally, curcumin inhibits ACE modulating angiotensin II synthesis and downregulating inflammation, while it also promotes fibrinolysis and the anticoagulation process [4,6,7] (Fig. 1). The antiviral actions of curcumin against multiple viruses (influenza and hepatitis viruses, herpes viruses, human papilloma virus, human immunodeficiency virus, severe acute respiratory syndrome coronavirus and other coronaviruses), bacteria and fungi have been established by experimental evidence [8]. Remarkably, recent evidence from in silico studies has demonstrated that curcumin prevents SARS-CoV-2 entry into cells by blocking the viral binding sites and the cell ligands (spike protein, ACE-2 receptors and basigin), downregulating trans-membrane serine protease 2 (TMPRSS-2), and by interfering with viral replication through the interaction with various viral proteins [4]. However, the minimal absorption of curcumin following oral administration presents a major limitation in its bioavailability [6].
Bromelain is a cysteine protease, isolated from the pineapple stem (Ananas comosus) [9]. Traditionally, it has been used for its anti-inflammatory and healing effects in cases of arthritis and injury, while it has been approved in Europe for the debridement of burn wounds. Experimental studies have demonstrated that bromelain presents unique immunomodulatory actions: 1) downregulation of the pro-inflammatory prostaglandin E2 (PGE-2) through inhibition of NF-kB and cyclooxygenase 2 (COX-2); 2)upregulation of the anti-inflammatory PGE-1; 3) activation of inflammatory mediators (interleukin 1b, interleukin-6, tumor necrosis factor-a and interferon-g) as an acute response to cellular stress, but also inhibition of inflammatory mediators in states of overt cytokine production; 4) modulation of T cell responses in vitro and in vivo; and 5) enhancement of T-cell dependent antigenspecific B cell antibody responses [5,10e14]. Importantly, bromelain exerts dose-dependent anticoagulant effects: 1) downregulation of PGE-2 and thromboxane A2 (TXA2), thus leading to relative excess of prostacyclin; 2) promotion of fibrinolysis by stimulating the conversion of plasminogen to plasmin and prevention of platelet aggregation. Bromelain also hydrolyzes bradykinin and reduces kininogen and bradykinin levels in serum and tissues, improving inflammation and edema as shown in animal studies [15]. Notably, the latter action supports a potential role of bromelain in alleviating COVID-19 symptoms such as cough, fever and pain, and the more serious implications of inflammation, thrombosis and edema. The effect of bromelain on PGE-2 inhibition exceeds that of prednisone and aspirin, presenting very low toxicity and no major side effects. Interestingly, a recent experimental study demonstrated that bromelain inhibits infection of VeroE6 cells by SARS-CoV-2 through blocking the virus binding and entry into cells via downregulation of ACE-2 and TMPRSS2 expression, and cleavage of the SARS-CoV-2 spike protein, presenting a novel promising therapeutic option that warrants further investigation.”
In summary, the combination of curcumin and bromelain are well positioned as supplements in people who are getting repetitive COVID-19/Spike protein exposure. Future randomized trials will elucidate the clinical benefits in specific applications.
Kritis P, Karampela I, Kokoris S, Dalamaga M. The combination of bromelain and curcumin as an immune-boosting nutraceutical in the prevention of severe COVID-19. Metabol Open. 2020 Dec;8:100066. doi: 10.1016/j.metop.2020.100066. Epub 2020 Nov 13. PMID: 33205039; PMCID: PMC7661945.
Pandemic and Panopticon: The Rise of the Biomedical Security State
By Janet Levy | American Thinker | April 20, 2023
The pandemic of 2020 saw the imposition of shocking restrictions. For the first time, healthy people were confined to their homes. Vaccines cleared for emergency use – meaning not rigorously tested – were forced on all citizens. Debate, even by scientists, was censored. Refusal to obey these arbitrary impositions could mean arrest, legal action, or, as Dr. Aaron Kheriaty found out, losing one’s job.
A psychiatry professor in good standing at the University of California at Irvine (UCI), Dr. Kheriaty became persona non grata when he demurred to the mandatory vaccine policy, claiming natural immunity as a Covid-recovered individual. Not caring for scientific debate, the university declared him a “threat to the health and safety of the community,” suspended him without pay, barred him from campus, and eventually fired him.
It did not matter that his psychiatry clerkship was the highest rated clinical course at UCI’s medical school; that he’d been chosen keynote speaker to address incoming medical students; and that when the pandemic broke out, he had risked his life to work long hours at the hospital, often uncompensated, while many colleagues stayed home in safety.
Uncowed, Dr. Kheriaty sued the university. In a more far-reaching action, he authored The New Abnormal: The Rise of the Biomedical Security State, a sober analysis and exposure of the tyranny of pandemic policies and the devastation they wrought. The book traces the roots of state interference in, and control of, the biomedical aspects of citizens’ lives to utilitarian ideas that began with Galton and Darwin, and trickled into eugenics, which he says is falsely viewed as entirely a creation of the Nazis when in fact American states were enforcing sterilization from the 1900s to the 1960s.
The core idea, he says, is this: the freedom of a citizen to make health and life decisions can be annulled by the state for the greater good, especially during emergencies. The questions it raises are: Who makes these decisions and on what basis? Who decides what is the greater good? Who is to be held responsible for errors of judgement? What checks and balances do we have, then, against the dictatorial inclinations of the powerful? Ancillary to the idea, he says, is the dangerous circular logic of the state of exception: those who declare an emergency in which citizens’ rights – including the right to question the declaration – stand suspended will believe that in that instance it is morally and politically justified!
We saw all that playing out during the pandemic. Kheriaty observes that the global elite and other political entities, in unbridled collaboration with intelligence and police powers, promoted the acceptance of biomedical surveillance. None of the extreme measures – lockdown, school closure, mandatory masking, vaccine mandates and passports – were subject to debate. No benchmarks were set to justify the emergency or identify when it would end. In fact, America continues to remain in a state of emergency (until May 11th).
Compliance was achieved through propaganda, policing, and surveillance. Guilt – Don’t Kill Granny – and Mao-style rousing – 15 Days to Stop the Spread – were deployed. Six-foot social distancing and curtailment of gatherings to no more than 10 people were imposed with no explanation of where these magic numbers came from. Human contact was redefined as a source of contagion. Exposure could build natural immunity, but this wasn’t acknowledged, for it would have potentially halved the profits of the $100 billion Covid vaccine industry.
Kheriaty identifies the characteristics of the biosecurity paradigm:
- a hypothetical risk, magnified to worst-case scenario to adduce grounds for maximum behaviorial control;
- systematic imposition of control on the entire citizenry, instead of vulnerable subsets;
- catastrophizing, in order to justify intrusive surveillance and the use of police and military action; and
- a merging of public health and the military-intelligence-industrial complex in developing and implementing tracking and data-mining capabilities.
Surveillance is the backbone of dictatorial regimes, and it was no different during the pandemic. In 2021, evidence emerged that the CIA had used digital surveillance to gather information on Americans sans judicial oversight or congressional approval. There were no safeguards to protect civil liberties. Such scenarios have long been envisioned – as far back as 1999, a possible smallpox outbreak was studied. Exercises such as Dark Winter, Atlantic Storm, Clade X, and Event 201 followed. They simulated imposition of martial law, detention of citizens, control of messaging, censoring dissent, enforcing mandates, and surveillance during public health crises. Recommendations to increase state power and use police or military intervention were subsequently embodied in the 2002 U.S. Public Health Security & Bioterrorism Preparedness & Response Act.
The religion of scientism took hold as Dr. Anthony Fauci, former chief medical advisor to the President, reframed the narrative on Covid, shifting the focus from the virus to viewing humanity as a vector. Fauci and a set of scientists and technocrats with broad powers arrogated to themselves a monopoly on knowledge and expertise. Lacking rational explanation, they used force, defamation of critics, and dubious promises of future outcomes to obtain public conformity to the security and surveillance measures.
The vast influence of Big Pharma over governments, the research establishment, and media, says Kheriaty, cannot be understated. Pfizer and Johnson & Johnson are wealthier than most countries, with vast sums available for lobbying. In 2020, 72 senators and 302 congressional representatives cashed campaign checks from the pharmaceutical industry. Biomedical researchers and medical journal editors receive payments from pharma. In a nine-year-period, two-thirds of all FDA reviewers took positions in the industry they regulated. The National Institute of Health, which owns half of the Moderna vaccine patent, chose to conduct internal testing of the vaccine rather than leave it to independent university-based researchers. Media acquiescence was achieved through $1 billion-worth of vaccine advertisements, paid for in taxpayer dollars!
Kheriaty goes so far as to assert that the lockdown was driven by an economic agenda disguised as public health protocol. It helped Big Pharma, multinationals, and the global elite who control them achieve the largest transfer of wealth in history by eliminating competition and spelling doom for small business.
The ultimate plan, devised by the global elite, is for a new world order, shifting government authority from sovereign states to powerful NGOs like the World Economic Forum (WEF), the International Monetary Fund (IMF), and the World Health Organization (WHO). Plans are afoot for a WHO-driven international pandemic treaty tied to a digital ID system, while IMF is promoting central bank digital currency (CBDC), which will allow complete tracking of monetary transactions. WEF chairman Klaus Schwab nurses transhumanist dreams, saying “we will not change what we do” but “who we are,” through gene- and bio-engineering.
The concluding chapter suggests ways of avoiding totalitarian emergencies and the abyss of the biomedical security state. He suggests strict limits on the declaration and control of emergencies, incorporating more checks and balances if necessary. He calls for substantive institutional reform that will eliminate the revolving door between Big Pharma and federal agencies. Besides, he says, the NIH monopoly must be broken, perhaps by distributing research grants to 50 state institutes of health that will focus on issues of local concern. Other ideas include provision of accurate, comprehensive information to allow people to give informed consent; allowing doctors to prescribe off-label or repurposed drugs and provide individualized care; holding Big Pharma accountable by bringing back product liability.
Freedom is at stake, as we discovered during the pandemic. Dr. Kheriaty lost his job, without a chance to defend himself, for daring to dissent. This – or much worse – can happen to any of us if we allow America to become the biomedical security state the global elite want to transform the world into.
Dr. McCullough Testifies in the Pennsylvania Senate
Four Domains of COVID-19 Vaccine Injury Syndromes Revealed
By Peter A. McCullough, MD, MPH | Courageous Discourse | June 9, 2023
On Friday June 9, 2023, I returned to the Pennsylvania Senate on request by former military officer and American hero, Senator Doug Mastriano (R-33). The session was co-chaired by Senator Cris Dush (R-25). Co-presenters included Steve Kirsch, Founder of the Vaccine Safety Research Foundation, and attorney Tom Renz. I organized my comments along the lines of this outline:
- Update on the US design and blueprint of SARS-CoV-2 from Baric et al at the University of North Carolina, Chapel Hill, funding by the NIH and outsourcing of the research plans via the EcoHealth Alliance to the Wuhan Institute of Virology, in Wuhan, China.
- COVID-19 vaccine injury syndromes
- Cardiovascular
- Neurological
- Thrombotic
- Immunological
- Questions from Senators and Representatives answered
- Shedding
- Risk benefit analysis of COVID-19 vaccines
- Failure of vaccine efficacy
- Reason why SARS-CoV-2 was created
- Global results of mass indiscriminate COVID-19 vaccination—winners and losers
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Former Insiders Criticize Iran Policy as U.S. Hegemony
By GARETH PORTER | CounterPunch | February 27, 2013
“Going to Tehran” arguably represents the most important work on the subject of U.S.-Iran relations to be published thus far.
Flynt Leverett and Hillary Mann Leverett tackle not only U.S. policy toward Iran but the broader context of Middle East policy with a systematic analytical perspective informed by personal experience, as well as very extensive documentation.
More importantly, however, their exposé required a degree of courage that may be unparalleled in the writing of former U.S. national security officials about issues on which they worked. They have chosen not just to criticise U.S. policy toward Iran but to analyse that policy as a problem of U.S. hegemony. … continue
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