In a recent study published in The Lancet Infectious Diseases, Watson et al. apply mathematical modeling to estimate that mass COVID-19 vaccinations saved between 14-20 million lives worldwide during the first year of the COVID-19 vaccinationprogram. Previous Brownstone [Institute] articles by Horst and Raman have already pointed out several erroneous assumptions in the study regarding infection- vs. vaccine-derived immunity duration as well as the fact it did not account for vaccine adverse events and all-cause mortality risk.
Here, I summarize the mechanics of how the authors arrived at their estimates of deaths averted due to mass vaccinations. I then elaborate on how flawed assumptions in the model can lead to grossly inflated estimates of averted deaths, which may explain the study’s lack of face validity and internal consistency. (See link for article)
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**Comment**
Please remember how another erroneous modelset this crazy-train in motion that grossly overestimated lives lost due to COVID. Ferguson’s“provably faulty information has arguably done more to move us into the era of medical martial law than any other single piece of misinformation. He was also the man behind a number of similarly over-the-top mortality projections in previous public health scares, including wildly faulty death forecasts for the 2005 bird flu scare and the 2009 swine flu scamdemic test run. So how does someone who consistently gets it so wrong get entrusted with constructing yet another faulty model for yet another public health scare? Hint: The Gates Foundation has 79 million reasons why. He was eventually tangled up in his own lies when he was caught cavorting with his mistress in direct contravention of the anti-social distancing rules that he so forcefully advocates for the peasants, but for some reason, despite making a big show of resigning in apparent disgrace for his actions, he is still advising the UK government on their scamdemic response.” Source
Seems the band plays on.
The conclusion in the opinion pieces states the faulty paper should not be used to inform public policy and guidelines, and that quantitative risk-benefit ratio analyses that use clinical trial or real-world datato compare risks of specific outcomes, such as all-cause mortality or myopericarditis following “vaccination” and coronavirus infection, are much more useful.
I’ll go one further.
This defunct, misleading article needs to be completely retracted.
Because you and I both know that it will be used ad nauseum to push dangerous gene-therapy injections on one and all, based on yet more faulty information that will be taken as gospel.
While the author posts a version of this article with figures and bibliography on ResearchGate, and tweeted the commentary to the original authors of the study in hopes for a response and rebuttal, he also submitted a shortened version to The Lancet Infectious Diseases and is awaiting their reply.
History is likely to record that the decision by a District Judge in Louisiana on Tuesday — allowing that state, along with the state of Missouri, to expose the bureaucrats imposing censorship through collusion with social media — marks a historic milestone victory for the First Amendment.
The First Amendment declares that “Congress shall make no law … abridging the freedom of speech, or of the press.” And yet bureaucrats in the executive branch often act as if the First Amendment doesn’t apply to them and have, over the past months and years, worked diligently to limit, restrict, cancel, and otherwise abrogate those precious freedoms with impunity.
Now, thanks to the ruling by Trump-appointed Judge Terry Doughty of the U.S. District Court of the Western District of Louisiana, Monroe Division, those bureaucrats’ days of hiding their identities from public view are shortly coming to an end.
(See link for article)
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SUMMARY:
As the AGs of those two states and their staffs can issue those “interrogatories and document requests,” the folks and platforms behind censoring will be exposed.
It all began in May when Missouri’s AG filed suit against Biden, Psaki, Fauci, and other ‘officials’ for allegedly colluding with social media companies to suppress freedom of speech under the guise of fighting ‘misinformation.’
Federal ‘officials’ have aggressively threatened to remove legal benefits on social media platforms if they do not censor disfavored speakers and content
Advertising agencies wield great power over public opinion, and prosecutors are increasingly starting to look at PR firms’ roles in cases where corporations are accused of serious malfeasance or fraud
Hundreds of climate-related court cases are now looking at the role advertising firms played in greenwashing
We’re seeing a similar trend happening in the drug industry, where ad agencies are starting to be held to account for the “legal lies” they spin on behalf of their clients. In February 2021, McKinsey & Company, a management consultancy firm, paid $573 million to settle a case in which they were accused of complicity by giving marketing advice to manufacturers of opiates, which have killed more than half a million people
May 6, 2021, Massachusetts Attorney General Maura Healey sued Publicis Health, accusing the company of “collecting more than $50 million in exchange for marketing schemes to get doctors to prescribe Purdue’s opioids to more patients, in higher doses, for longer periods of time.” Publicis tried to have the case dismissed, but failed
Aside from hiring big advertising companies to push their wares, drug companies keep the truth from being known through the use of ‘fact checkers’
Advertising agencies wield great power over public opinion, and prosecutors are increasingly starting to look at PR firms’ role in cases where corporations are accused of serious malfeasance or fraud. For example, CampaignAsia.com recently reported that:1
“Hundreds of new greenwashing-related court cases have increased the pressure on PR and advertising agencies, as prosecutors begin to widen their net in terms of who should bear responsibility for the controversial practice …
Since May 2021, 369 climate-related lawsuits against agencies have been concluded, with 218 of those (58%) ruling against the PR and advertising firms … Over the past five years the number of lawsuits relating to the role of PR and advertising in climate change has doubled. The cases are mainly US-based, but span 39 countries in total.”
Smoke and Mirrors
The data reported by CampaignAsia come from the report,2 “Smoke and Mirrors: The Legal Risks of Fossil Fuel Advertising,” published in May 2022 by a climate-change activist organization called Clean Creatives.
The report names WPP, IPG, Dentsu, Publicis and Omnicom — four holding companies that in turn run dozens of individual PR agencies — as being particularly vulnerable to greenwashing lawsuits, as they all work to improve the public image of fossil fuel clients “while they continue to pollute the earth.”
According to Clean Creatives director Duncan Meisel, PR companies take “significant reputational, business and legal risks when they work with fossil fuel companies to spread climate disinformation,” as their work not only hurts the planet but could also land them in court. Meisel also warns that ad agencies may be duped themselves by clients who withhold damaging information, and that such naiveté could end up being costly.
The ESG Scam
Investing in “green” companies has skyrocketed in recent years, but many of these companies aren’t what they claim to be. According to climate change think tank InfluenceMap, a majority of “green” equity funds fall short.
Of the 723 funds marketed using Environmental, Social and Governance (ESG) claims, more than half failed to meet the Paris Accord rules on carbon emissions and clean energy, and “more than 70% of the funds with broader ESG goals are also misaligned with global climate targets,” Time magazine reported.3
InfluenceMap noted that BlackRock Inc. — the world’s largest investment firm, which has vowed to make sustainability a core investment strategy — still invests in fossil fuels. The same goes for other major investment companies.
State Street Corporation, for example, which is the third largest, owns a portion of Marathon Petroleum and Philips 66 which, according to InfluenceMap, are “two of the world’s most egregious fossil fuel lobbying companies preventing policy-based climate action.”4
Similarly, a May 2021 report5 by the Economist concluded some of the largest ESG funds in the world are “stuffed full of polluters and sin stocks.” According to a 2019 report by the Wall Street Journal,6 “Eight of the 10 biggest U.S. sustainable funds are invested in oil-and-gas companies, which are regularly slammed by environmental activists.”
Aside from oil and gas, other top ESG investments include tobacco companies and casino operators,7 neither of which is particularly well-known for high ethical standards. In a March 2021 USA Today op-ed, former chief information officer of sustainable investing for BlackRock, Tariq Fancy, said the quiet part out loud:8
“In truth, sustainable investing boils down to little more than marketing hype, PR spin and disingenuous promises from the investment community.”
McKinsey & Company Fined for Consulting That Led to Deaths
We’re also seeing a similar trend happening in the drug industry, where ad agencies are starting to be held to account for the “legal lies”9 they spin on behalf of their clients.
For example, in February 2021, McKinsey & Company, a management consultancy firm, paid $573 million to settle a case in which they were accused of complicity by giving marketing advice to manufacturers of opiates — including the maker of Oxycontin, Purdue Pharma — which have killed more than half a million people.10 CampaignAsia writes:11
“Lauren Papenhausen, a partner at White & Case, said the McKinsey settlement is ‘particularly noteworthy in that it signals a willingness on the part of the government to pursue not only manufacturers, but also those who provide them professional services.
While one might view the settlement as unique to the particular context of opioids, it raises the question of whether governmental concern over particular marketing strategies is a sign of enforcement efforts to come.’”
A late June 2022 article by Johns Hopkins Bloomberg School of Public Health also highlighted obtained litigation documents12 showing McKinsey’s role in the opioid epidemic:13
“They show how McKinsey advised opioid makers Purdue Pharma, Endo Pharmaceuticals, Johnson & Johnson and Mallinckrodt to help them increase sales, despite the growing public outcry over the opioid epidemic …
Materials include scopes of work, proposals, and invoices; presentations prepared for internal discussion and for clients (including Purdue Pharma and Endo Pharmaceuticals); spreadsheets outlining project staffing; and emails responding to news about increased restrictions on opioids.
The collection also houses letters from regulatory agencies, including the U.S. Food and Drug Administration, in response to new drug applications from opioid manufacturers; preparation materials for regulatory advisory committee meetings; opioid-related transition documents for state and federal agencies; and other internal files.
‘These documents now form a unique and invaluable public resource to help us comprehend the magnitude of harm done to the millions of Americans affected by the opioid crisis,’ said Jeremy Greene, MD, PhD, MA, William H. Welch Professor of Medicine and the History of Medicine in the Johns Hopkins School of Medicine.
‘More generally, they shine a bright light on the murkier intersections of science, industry, and financial interest that continue to characterize the U.S. health care system’ …
‘Researchers can leverage these litigation documents to see patterns of industry behavior that could be regulated to protect public health,’ said Dorie Apollonio, PhD, MPP, a professor of clinical pharmacy in the UCSF School of Pharmacy. ‘This will be critical to identifying reforms that can protect against future epidemics like this.’”
McKinsey Played Both Cop and Robber
We recently discovered that the situation is even more corrupt than previously thought. A U.S. House investigation14,15,16 into McKinsey, based on materials obtained through the discovery process of various lawsuits, also revealed McKinsey was advising the U.S. Food and Drug Administration on the safety of opioids, while at the same time advising drug companies on how to maximize sales.
In one instance, McKinsey wrote scripts for Purdue to use in its meeting with the FDA to discuss the safety of OxyContin in pediatric populations. In another, Jeff Smith, a senior McKinsey consultant, worked on a risk evaluation and mitigation strategy (REMS) for OxyContin while simultaneously advising the FDA about the drug’s safety.17
As noted by investigative journalist Paul Thacker,18 “Just think about that for a moment — for years McKinsey played both cop and robber.” As reported by The New York Times, April 13, 2022:19
“Since 2010, at least 22 McKinsey consultants have worked for both Purdue and the FDA, some at the same time, according to the committee’s 53-page report …
The firm provided no evidence to the committee that it had disclosed the potential conflicts of interest as required under federal contracting rules — an ‘apparent violation,’ the report said. McKinsey also allowed employees advising Purdue to help shape materials that were intended for government officials and agencies …
‘Today’s report shows that at the same time the FDA. was relying on McKinsey’s advice to ensure drug safety and protect American lives, the firm was also being paid by the very companies fueling the deadly opioid epidemic to help them avoid tougher regulation of these dangerous drugs,’ Representative Carolyn Maloney, the New York Democrat who chairs the committee, said in a statement …
A bipartisan group of lawmakers last month introduced legislation20 aimed at preventing conflicts of interest in federal contracting, citing McKinsey’s experience with Purdue and the FDA.”
McKinsey Engaged in Direct Sales
Now, we’ve also come to find that McKinsey21 did direct sales for its Big Pharma clients, using in-house sales reps. They actually employed entire sales teams that sold clients’ drugs directly to doctors. This revelation came out of the repository22 of opioid litigation documents set up by Johns Hopkins Bloomberg School of Public Health. Emails23 show Publicis offers a similar service where Publicis sales staff sell clients’ products to pharmacies. As reported by The New York Times:24
“The Times found that the firm played a far deeper and broader role in advising clients involved in the opioid crisis than was publicly disclosed … While the firm held remarkable sway at Purdue, it also advised the largest manufacturer of generic opioids, Mallinckrodt. It worked with Endo on marketing Opana and helped it grow into a leading generics manufacturer.
It advised Johnson & Johnson, whose subsidiary Tasmanian Alkaloids was the largest supplier of the raw materials extracted from poppies used to make many top-selling opioids. Then, as the full brunt of the epidemic became apparent, it counseled government agencies on how to address the fallout …
Drawing on reams of data and proprietary tools, McKinsey vetted deals and advised on corporate strategy. It developed tactics for dealing with regulators and helped secure approval for new products.
The firm helped clients adopt more aggressive sales strategies, which, on at least two occasions, led companies to shift resources to more potent products.
It profiled and targeted physicians, in some instances trying to influence prescribing habits in ways that federal officials later warned heightened the risk of overdose. And when opioid prescriptions began to decrease during a government crackdown, the records show, McKinsey devised new approaches to drive sales.”
Publicis to Face Charges Over Role in Opioid Crisis
Another advertising company that is in hot water over its role in the opioid crisis is Publicis Health, which crafted many of Purdue’s Oxycontin marketing materials.
Massachusetts Attorney General Maura Healey sued Publicis Health May 6, 2021, accusing the company of “collecting more than $50 million in exchange for marketing schemes to get doctors to prescribe Purdue’s opioids to more patients, in higher doses, for longer periods of time.”25 Publicis tried to have the case dismissed, but failed.26
The Truth About Fact Checkers
Aside from hiring big advertising companies to push their dangerous wares, how else are drug companies keeping the truth from coming out? Enter fact checkers. Over the past two years, it’s become quite clear that so-called “fact checkers” are anything but. While they claim to combat misinformation, they’re the ones spreading most of it, and they do it on behalf of the drug industry and the advertising companies that run cover for them.
There are countless examples of conflicts of interest running amuck in fact checking organizations. To list just a few examples:
• Publicis funded the creation of and is partnered with NewsGuard,27 an online “credibility rater”28 to “provide its clients with more responsible, trustworthy advertising platforms.” It’s not far-fetched to assume Publicis might influence NewsGuard’s ratings of drug industry competitors, such as alternative health sites.
NewsGuard’s health-related service, HealthGuard, is also partnered with the Center for Countering Digital Hate (CCDH) — a dark money-funded progressive cancel-culture leader29 with extensive ties to government and global think tanks that has labeled people questioning the COVID-19 injection as “threats to national security.”
• As a Google partner,30,31 Publicis also has the ability to bury undesirable views that might hurt its clientele.
• Pfizer (a Publicis client32) also funds Facebook’s fact checking operation,33 which is why you can’t say anything negative about the COVID jabs on Facebook.
• Pfizer also has significant conflicts of interest with Reuters, which has joined in the fact checking enterprise.34 Reuters chairman (and former CEO) James Smith is both a top investor and board member of Pfizer,35 raising suspicions he might have a vested interest in keeping Pfizer’s media record clear of incriminating details.
• Another fact checking organization called FactCheck.org is funded, in part, by the Robert Wood Johnson Foundation, which holds nearly $2 billion in Johnson & Johnson stock. What’s more, its CEO, Richard Besser, is a former (2009) director of the U.S. Centers for Disease Control and Prevention, which appears to view the protecting of Big Pharma interests as a full-time job.
The Ultimate Goal of This Network
This network of players is also intricately tied to the World Economic Forum (WEF), which is using pandemic fears to usher the world into a “Great Reset.”Publicis is a WEF partner,36 as is Pfizer, Johnson & Johnson, Google, BlackRock, State Street and a slew of other investment firms — and oil companies.37
Many fact checking organizations belong to the International Fact-Checking Network,38 which is financed by George Soros (through his Open Society Foundation and the National Endowment for Democracy), Google and the Bill & Melinda Gates Foundation39 — all of whom are part of the WEF’s technocratic cabal that is pushing for a Great Reset.
This sort of brings us back to where we started, with the greenwashing of polluters. The entire “green” agenda serves that larger “Reset” goal, and the fact that we’re now seeing so much greenwashing going on in the “green” investment sphere is just more proof that the whole thing is a scam. The claim that we must quit using fossil fuels and “go green” to save the planet is a ruse to get people to accept a radically lowered quality of life and greater restrictions on freedom.
Big Pharma fits into this larger scheme because the WEF needs a justification for the introduction of biomonitoring and biosecurity in the form of a digital vaccine passport. The COVID pandemic was a manufactured crisis that “necessitated” global vaccination, and a way to confirm vaccination.
Vaccination tracking was the chosen foundation for what will become a much larger and more invasive monitor and control system involving your finances as well. With vaccine passports being largely rejected, plan B is to introduce digital identity, which is more or less the same thing, just more complete from the start.
So, the reason these players — from fund managers to PR companies, drug companies, legacy media, social media platforms, search engines and fact checking organizations — are all protecting each other is because they’re all cogs in the same machine.They work together to achieve an ultimate goal, which is to put the world population under a system of global technocratic control.
How CDC Blatantly Uses Weekly Reports to Spread COVID Disinformation: Three Examples
The authors of the Centers for Disease Control and Prevention’s Morbidity and Mortality Weekly Report are afforded the luxury of broadcasting their findings to massive audiences through media outlets that don’t hold them accountable for even gross lapses in scientific rigor.
The Centers for Disease Control and Prevention (CDC) — the primary U.S. health protection agency — publicly pledges, among other things, to “base all public health decisions on the highest quality scientific data that is derived openly and objectively.”
The CDC’s “primary vehicle for scientific publication of timely, reliable, authoritative, accurate, objective, and useful public health information and recommendations,” according to the agency, is its Morbidity and Mortality Weekly Report (MMWR).
The CDC states that the MMWR readership consists predominantly of physicians, nurses, public health practitioners, epidemiologists and other scientists, researchers, educators and laboratorians.
However, these weekly reports also serve as the means by which the agency disseminates its scientific findings to a much wider readership through media outlets that inform hundreds of millions of people.
(See link for article)
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SUMMARY:
MMWR is not peer-reviewed & often misrepresents or omits important facts
The CDC uses weak or flawed data to make public health decisions. Three examples:
March 5, 2021, MMWR: “Mask mandates were associated with statistically significant decreases in county-level daily COVID-19 case and death growth rates within 20 days of implementation.”
But the authors’ own data and calculations show the drop in DGR may have had nothing to do with mask mandates at all. How amazing! Masks seem to work several weeks before people are forced to wear them! The CDC arbitrarily chose to limit its analysis to 100 days after mandates were instituted & has a lengthy history of using arbitrary cut offs. Yet the media continually reported on the flawed mask study & more than 100 media outlets cited the CDC study within 24 hours of its release — but not one questioned the authors’ analysis.
Three days after the flawed mask study, CDC’s Walensky stated that “fully vaccinated people can congregate indoors with other fully vaccinated people without wearing face coverings or practicing physical distancing.”
Jan. 7 MMWR, “CDC recommends COVID-19 vaccination for women who are pregnant, recently pregnant (including those who are lactating), who are trying to become pregnant now, or who might become pregnant in the future to reduce the risk for severe COVID-19–associated outcomes.”
The CDC relied on comparing two poorly matched groups of mothers that set up the unvaxxed group to be at higher risk:
50% of the unvaxxed had inadequate prenatal care than the “vaxxed”
Obesity was overrepresented in the unvaxxed group than the “vaxxed”
3 times more African American women were in the unvaxxed group (CDC admits these mothers may have as much as a 50% greater risk for preterm birth compared to white mothers)
25% of the unvaxxed group had a greater incidence of COVID infection
Scarcity of “vaxxed” moms ‘vaccinated’ in the 1st trimester where the risk of defects and miscarriages is greatest.
This flawed study showed that COVID shots aren’t just safe, they actually lower the risk of preterm birth and low birth size. Mainstreammediajumped right on this flawed study.
April 19 MMWR, CDC authors compared the risk of hospitalization of 5- to 11-year-old children from COVID-19 during three different time periods: pre-Delta, Delta and Omicron. Statements are made in the text of the paper that are true but also irrelevant or misleading. Instead of using total number of hospitalizations, they again arbitrarily choose a brief period of each wave which suggest Omicron is more dangerous than Delta which is blatantly false. They use the same strategy in March, and Dr. Nass dissects it here.
CDC authors don’t mention the absolute risk of the intervention, but only the relative benefit of the experimental vaccine as well as the fact roughly 10,000 children had to be fully vaccinated to prevent a single hospitalization.
The CDC also misleads by stating 87% of hospitalized children were unvaxxed at a time when 70% or more hadn’t been inoculated during the time frame. Mediaoutlets fell all over themselves in announcing this flawed study, and on this page, there are dozens of articles citing the misleading MMWR.
The data from the MMWR has bee updated and now show that more than 113,000 children in that age group must receive both doses to prevent a single hospitalization per month.
The CDC states: “Increasing COVID-19 vaccination coverage among children aged 5–11 years, particularly among racial and ethnic minority groups disproportionately affected by COVID-19, can prevent COVID-19–associated hospitalization and severe outcomes,” but their own data show this is false. The authors later correct themselves in the body of the report: “There were no significant differences for severe outcomes by vaccination status,” yet which statement do you think the media outlets chose to publish?
If the MMWR series is “the voice of CDC,” mainstream media serves as its mouthpiece.
By working together, the CDC authors are afforded the luxury of broadcasting their findings to massive audiences through media outlets that will not — and in many cases cannot — hold them accountable for even gross lapses in scientific rigor.
In Conclusion:
There wasn’t a “statistically significant decrease in COVID-19 case counts associated with mask mandates.”
There wasn’t enough data to recommend the COVID-19 vaccine for mothers who recently became pregnant.
The data did not demonstrate that the COVID-19 vaccine can prevent severe outcomes in children ages 5 to 11.
ACTION ITEM: SHARING IS CARING. THE BEST THING YOU CAN DO IS SHARE THIS ON SOCIAL MEDIA AND TAG PHYSICIANS. SECOND BEST? GIVE THEM A GIFT SUBSCRIPTION, BELOW.
Most people do not know what negative vaccine efficacy is. Nor do they know the difference between vaccine efficacy and vaccine effectiveness. We’re changing that by teaching the world the Math of Vaccine Science this fall.
Measures like these require data. And Dr. Peter McCullough reviewed data for two hours in Grand Rapids, Michigan this weekend to a crowd of doctors and lay people. He sent me his slides. I’m presenting these slides to you without commentary – but with links to each resource he cites so you can share this Substack article with physicians and scientists who are beginning to scratch their heads. They are vaccinated, so why are they getting COVID? They are beginning to ask themselves: Why are such a high percentage of people who get serious COVID-19 vaccinated, when the promise was that the vaccine would prevent this? And why, if the vaccine is such a success, have only 21% of Americans taken their first booster? In that setting, why is Fauci proposing a “second” booster … and boosters likely every few months?
Popular Rationalism is a reader-supported publication. To receive new posts and support my work, consider becoming a free or paid subscriber.
I thank Dr. McCullough for sharing his slides with all of us. You can download the slidedeck here. To access the resource cited on each slide, click the image. Be sure to note the specific data Dr. McCullough highlighted, when he has.
Feel free to download these images and share them on social media with the cited link. Please also link to the United Healthcare Summit video here:
Verbal Public Comment – July 19-20, 2022 Meeting (With References)
Carl Tuttle
Hudson, NH, United States
Jul 19, 2022 —
Please see my verbal public comment below read aloud at today’s TBDWG meeting. A copy of this comment and supporting references were sent to all members of the Working Group via email…
My verbal comment today is a follow-up to my Written Public Comment regarding the CDC’s refusal to recognize the disabling stage of Lyme disease.
I would like to point out that maternal-fetal transmission of Lyme disease was identified in 1985 by Dr. Allen Steere [1] but has gone unrecognized by the IDSA, CDC and NIH until the Patient Centered Care Advocacy Group last year demanded that the Infectious Diseases Society of America remove its false statement that Lyme is only transmitted by a tick. [2] The NIH has now issued a series of notices to encourage investigators to apply for grants 36 years after congenital Lyme disease was first identified. A Lyme treating physician here in NH has told me that they are seeing Lyme disease in generations of patients.
There has been no new treatment for Lyme disease in that same timeframe except from those on the frontlines who are witnessing the devastation first hand. Dr. Horowitz has published success with dapsone combination therapy. [3] Dr. Liegner has published success with “Repurposing” Disulfiram in the Treatment of Lyme Disease and Babesiosis. [4]
Physicians who treated Lyme disease with long-term antibiotics have lost their license to practice because they questioned the official narrative. Many states have passed laws to protect these clinicians from being harassed by state medical boards. We have witnessed the same response with early treatment for Covid. Long-term antibiotics would give the public a reason not to take a Lyme vaccine just as early Covid treatment with ivermectin gave the public a choice to opt out of the experimental jab.
In 2003 Texas physicians Harvey and Salvato tested their chronically ill patients for Lyme disease via CDC Western blot criteria finding all patients positive for the infection in a state where the prevalence of Lyme infected ticks is only about 1-2%. [5] “No history of bull’s-eye rash or illness following tick bite was reported by these patients.” The CDC defines “Lyme disease” exclusively as a zoonotic illness. Congenital and gestational transfer cases have been disregarded for reasons not evident to us”.
Where are the studies for sexually transmitted Lyme disease and why has this mode of transmission been completely ignored for three decades?
What is the point of all this you might ask? It is quite obvious that there has been a concerted effort to control the narrative through suppression of the truth, facts and scientific references.
As mentioned in my Written Public Comment, [6] the only action item we have in the pipeline after thirty years is a vaccine fast-tracked by the FDA in 2017. [7] Since all of the eggs have been put into the vaccine basket it would appear that our Health Agencies are in the shot business with annual revenue of $4.3 billion from the sales and patent royalties. [8]
A chronic relapsing seronegative disease doesn’t fit the vaccine model so deny the chronically infected and your patents for vaccines and diagnostic technology continue to reap patent royalties. The federal watchdog is no more. People suffering and dying and for what? Lyme for Profit.
The CDC has propagated a false Lyme disease narrative for decades and to this day refuses to recognize the disabling stage of Lyme disease. Wake up America!
‘Like a Horror Movie’: Top Scientists Alarmed and Embarrassed by Agencies’ Failure to Follow Science on COVID
Top doctors and scientists at the leading U.S. public health agencies are “frustrated, exasperated and alarmed” about the direction of the agencies they work for, according to the authors of a Substack post. They’re also embarrassed — about “bad science.”
Top doctors and scientists at the leading U.S. public health agencies are “frustrated, exasperated and alarmed” about the direction of the agencies they work for, according to the authors of a Substack post published last week.
They’re also embarrassed — about “bad science.” And many are leaving.
“It’s like a horror movie I’m being forced to watch and I can’t close my eyes,” said one senior official with the U.S. Food and Drug Administration (FDA). “People are getting bad advice and we can’t say anything.”
The comment was one of many culled from calls and text messages between officials and the article’s co-authors, Marty Makary M.D., M.P.H., and Tracy Beth Høeg M.D., Ph.D.
Makary and Høeg said the officials who spoke to them agreed to be quoted — but only anonymously, for fear of professional repercussions.
The National Institutes of Health (NIH) and the Centers for Disease Control and Prevention (CDC) are plagued with “low morale” and “high turnover,” officials told Makary and Høeg.
“At the NIH, doctors and scientists complain to us about low morale and lower staffing: The NIH’s Vaccine Research Center has had many of its senior scientists leave over the last year, including the director, deputy director and chief medical officer,” they wrote.
And it’s no better at the CDC, they said:
“The CDC has experienced a similar exodus. ‘There’s been a large amount of turnover. Morale is low,’ one high-level official at the CDC told us. ‘Things have become so political, so what are we there for?’ Another CDC scientist told us: ‘I used to be proud to tell people I work at the CDC. Now I’m embarrassed.’”
Officials complained the heads of their agencies “are using weak or flawed data to make critically important public health decisions, that such decisions are being driven by what’s politically palatable to people in Washington or to the Biden administration and that they have a myopic focus on one virus instead of overall health.”
One CDC scientist told Makary and Høeg about the shame and frustration within the agency over what happened to U.S. children during the pandemic.
The scientist said:
“CDC failed to balance the risks of COVID with other risks that come from closing schools. Learning loss, mental health exacerbations were obvious early on and those worsened as the guidance insisted on keeping schools virtual. CDC guidance worsened racial equity for generations to come. It failed this generation of children.”
The CDC also ignored natural immunity, according to some officials who declined to be named. “The vast majority of children have already had COVID, but this has made no difference in the blanket mandates for childhood vaccines.”
By mandating “vaccines and boosters for young healthy people, with no strong supporting data, these agencies are only further eroding public trust,” they added.
“I can’t tell you how many people at the FDA have told me, ‘I don’t like any of this, but I just need to make it to my retirement,’” one official told Makary and Høeg.
Commenting on the revelations, Robert F. Kennedy, Jr., Children’s Health Defense chairman and chief legal counsel, told The Defender, “The 33-year devolution of NIH from the world’s premier bio research agency into Big Pharma’s servile marketing subsidiary has been an excruciating downfall for NIH’s dwindling cohort of researchers and scientists of integrity.”
Kennedy added:
“The COVID-19 catastrophe exposed to the world that NIH no longer does science or public health and confronted remaining employees with the dilemma that working at NIH means living against conscience. The current exodus captures the last remaining NIH officials who still have one.”
Makary and Høeg said it’s statistically impossible for everyone who works inside U.S. health agencies to have 100% agreement about “such a new and knotty subject.”
“The fact that there is no public dissent or debate can only be explained by the fact that they are — or at least feel that they are — being muzzled,” they wrote. “It is an ancient, moral requirement of our profession to speak up when we believe questionable treatments are being proposed. It is also good for the public.”
“The leaders of the CDC, the FDA and the NIH should welcome internal discussion — even dissension — based on the evidence,” they wrote. “Silencing physicians is not ‘following the science.’”
Makary: COVID vaccines for kids at center of controversy
In a July 17 interview on “Fox & Friends,” Makary said senior officials — including all three leaders of the vaccine research center at the NIH and top experts at the FDA — are leaving because they see problems with the data and are frustrated.
“The top two vaccine experts at the FDA [in September 2021] quit in protest over political interference, and many people at the CDC told me that people are getting bad advice and we can’t say anything,” he said. “They’re not allowed to go to the media, and at the center of it is the treatment of children.”
“In the subgroup of children aged six months to two years, the [Pfizer] trial found that the vaccine could result in a 99% lower chance of infection — but that they also could have a 370% increased chance of being infected.
“In other words, Pfizer reported a range of vaccine efficacy so wide that no conclusion could be inferred. No reputable medical journal would accept such sloppy and incomplete results with such a small sample size. More to the point, these results should have given pause to those who are in charge of public health.”
Yet, without that clinical data, they’re still “pushing vaccines for infants and toddlers, for people who already had COVID and boosters for young children,”Hegseth said.
“That’s right. And parents are not falling for it after nearly a month of the government heavily pushing vaccines in kids under 5,” Makary said. “Only 3% of parents have chosen to get their kids under 5 vaccinated. More parents believe in UFOs I think.”
CDC Director Dr. Rochelle Walensky said “people are eager to get their kids vaccinated,” but this is not the case, Makary told Hegseth. Because the “vaccine trial in kids under 5 failed” — the “study was done and it showed no benefit.”
Makary said:
“Now why are we even doing clinical trials if when you get a negative result showing it has no benefit, they’re approving it anyway? You’re making a mockery of the process. This is what people within the agencies are very frustrated about. This is why they’re leaving.
“Moderna’s vaccine had a 4% efficacy and Pfizer, the results were so bad with no statistical significance that one of the internal people within the CDC said that you can inject a child with the vaccine or squirt it in their face and you’ll get the same benefit.”
“If the CDC wants to win some respect back, apologize and show some humility and less absolutism,” he added.
In their article, Makary and Høeg said there’s also an issue of how long a COVID-19 vaccine gives protection, as data in adults show that protection wanes in “a matter of months” and there’s “no such data for young children.”
“It seems criminal that we put out the recommendation to give mRNA Covid vaccines to babies without good data,” a CDC physician told Makary. “We really don’t know what the risks are yet. So why push it so hard?”
“The public has no idea how bad this data really is,” a high-level FDA official told Makary and Høeg. “It would not pass muster for any other authorization.”
“And yet, the FDA and the CDC pushed it through,” Makary and Høeg wrote. That “slap in the face of science may explain why only 40% of parents in rural areas say their pediatricians did not recommend the Covid vaccine for their child.”
White House calling the shots
In a July 15 interview with Tucker Carlson, Makary said doctors everywhere in the world, even in the government, should “always be free to speak up about their public health concerns.”
Yet, right now in the government, “doctors are muzzled.”
“I talked to many doctors for this piece, at NIH and CDC, who are extremely frustrated,” Makary told Carlson. “They’re smart people. They know vaccine efficacy of 4% doesn’t warrant authorization. They also know there’s no health emergencyright now among kids six months of age.”
Makary said he learned a lot from interviewing anonymous top officials, and they’re being silenced:
“They know the underlying data. They know it’s inappropriate. They’re not allowed to speak to anyone. If a reporter calls, the communications office has to approve the conversation and if they want to ask the scientist whether or not they want to do this. Tell us what you’re going to tell the reporter and then we’ll decide whether or not to approve it.”
“At the CDC, a bunch of scientists actually said ‘look we recognize the insanity of mass testing — trying to take down every case of the virus in the United States,’” Makary told Carlson. “So they came up with a plan to use sampling data like we do with influenza every year to get better numbers from the hospital of those truly in there for COVID, not just everybody with incidental COVID tests.”
Makary said he was told by top officials the plan was “rejected by the White House.”
“I heard from smart people who were just extremely frustrated that not only are they bypassing the normal scientific process, you really can’t say anything because if they do, they know their jobs are at risk and they’ll be treated very differently,” Makary told Carlson.
“One person said there’s no transparency as to how Dr. [Anthony] Fauci makes his decisions, he doesn’t even consult with the real experts.”
Dr. Jay Bhattacharya, professor of Medicine at Stanford University and a research associate at the National Bureau of Economic Research, praised the “blockbuster article” that confirmed scientists are being subject to tremendous political pressure to distort COVID-19 science and vaccine recommendations.
An absolute blockbuster article by @TracyBethHoeg and @MartyMakary. Insider interviews with @CDCgov and @NIH scientists reveal tremendous political pressure to distort covid science and vax recommendations. Our public health agencies are in disarray. Excellent reporting! https://t.co/yx1SQXFWL4
Responding to Makary’s interview with Carlson, Dr. Peter McCullough said in a tweet that the FDA needs “immediate oversight and ordered to retract EUA approval.”
Dr. Makary on @TuckerCarlson explains they failed in the toddler RCTs with inadequate efficacy and FDA EUA approval was fraud. Gross regulatory misconduct. FDA needs immediate oversight and ordered to retract EUA approval. Worse yet, no assurances on long-term safety in kids. pic.twitter.com/4fslNbPD8R
— Peter McCullough, MD MPH (@P_McCulloughMD) July 17, 2022
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