For several weeks I have been messaging the scientific community and the public about an approach addressing the burden of SARS-CoV-2 Spike protein in tissues and organs in the human body that is largely responsible for post-COVID and vaccine injury syndromes.
No therapeutic claims can be made since large, prospective, double-blind randomized, placebo-controlled trials have not been completed on any of the compounds mentioned in this paper. I checked clinicaltrials.gov and no such trials have been planned. The Biden HHS US Action Plan for Long-COVID Research has pumped a billion dollars into long-COVID research and no new therapies have emerged. HHS, NIH, CDC, FDA have not recognized the larger issue of vaccine damage to the body.
At three and one half years into the pandemic and two and a half years into the COVID-19 vaccine debacle, myself and my clinic partners formulated a baseline regimen upon which additional drugs or agents can be added. We believe the Spike protein and the inflammation caused by it and its proteolytic fragments are at the heart of the pathophysiology we are observing.
We searched the literature for all available sources of evidence for products that can aid the human body in breaking down and catabolizing the Spike protein. We found two compounds, nattokinase and bromelain. Both of which additionally have fibrinolytic properties which are advantageous in the prothrombotic milieu induced by the persistent Spike protein. Curcumin was added for its anti-inflammatory properties in the setting of post-COVID and vaccine patients. The main safety caveats are bleeding and allergic reactions, both of which are manageable. It is our experience that both nattokinase and bromelain can be used in addition to antiplatelet and anticoagulant drugs with physician monitoring.
The empiric regimen can be continued for 3-12 months or more and be guided by clinical observation:
-Nattokinase 2000 FU (100) mg orally twice a day without food
-Bromelain 500 mg orally once a day without food
-Curcumin 500 mg orally twice a day (nano, liposomal, or with piperine additive suggested)
McCullough PA, Wynn C, Procter BC. Clinical Rationale for SARS-CoV-2 Base Spike Protein Detoxification in Post COVID-19 and Vaccine Injury Syndromes. Journal of American Physicians and Surgeons Volume 28 Number 3 Fall 2023, 90-93.
The full manuscript is linked and serves as your reference. While we are seeing case examples of improvement, we aim to collaborate with others as we did with the McCullough Protocol, to demonstrate clinical effectiveness of Base Spike Detoxification as a fundamental strategy for a large number of individuals who have suffered long-term consequences from SARS-CoV-2 infection and COVID-19 vaccination.
The Office for National Statistics (ONS) have finally published their ‘Deaths by vaccination status, England’ dataset. This is for deaths occurring between 1 April 2021 and 31 May 2023.
I know many people consider these data unreliable but I always have a look at it nevertheless.
To assess whether the vaccine is safe I decided to look at all cause deaths separated by vaccine status (Table 5). This shows the number of all cause deaths for the unvaccinated and ‘ever vaccinated’ by month. It is also separated by age group (18-39; 40-49; 50-59; 60-69; 70-79; 80-89 & 90+).
For each month I looked at the total number of deaths and calculated what percentage of those deaths were in the ‘ever vaccinated’ category. So if there were 30 unvaccinated deaths and 70 vaccinated deaths, the percentage of ‘ever vaccinated’ deaths would be 70%.
This doesn’t really tell us anything, however. The headline might be shocking, e.g. ‘90% of deaths occurring in the vaccinated’ but if 90% of the population are vaccinated then that is to be expected.
However, if a higher percentage of deaths are occurring in the vaccinated (than the percentage of people vaccinated), then perhaps the vaccines are causing some harm. There are many confounders which confuse things but it is at least a signal that something is up and should be looked at. For example if 90% of the country is vaccinated but 95% of deaths are in the vaccinated then perhaps the vaccine is causing the additional 5% of deaths.
So, I took the data showing the percentage of people vaccinated with at least one dose from the UK government website, cleaned it up so that it matched the ONS formatting and created a few graphs.
You can see that in the 18-39 age group, as the vaccine rollout started, there was a higher percentage of deaths in the vaccinated versus the number of people vaccinated. This may have been because sick or immunocompromised people were vaccinated first. The two percentages then quickly merged before beginning to separate again in mid 2022.
This is also the exact time when excess deaths began to skyrocket. Ever since that point, the percentage of deaths in the ‘ever vaccinated’ group has been higher than the percentage of people vaccinated.
Here are the graphs for the other age groups.
You can see that in all the age groups, except for the 50-59 year olds, the percentage of all cause deaths in the ‘ever vaccinated’ group is higher than the percentage of that group that is vaccinated. The data for the 80-89 and 90+ groups are particularly shocking.
Worthy of an investigation? Of course not. Instead the NHS is launching a £50,000 probe to uncover why NHS staff aren’t getting Covid and flu jabs. Probably because they can see the data presented above with their own eyes.
I read today that a new RSV vaccine has just been approved by the FDA for expectant mothers. I know from previous articles I’ve written that an RSV vaccine for children is also on the fast track to get on the all-important childhood immunization schedule.
I’m sure we’ll all read about how RSV is one of the greatest killers of children … and thus we have yet another vaccine that’s a Godsend. (The above-linked Wall Street Journal story tells us approximately 300 children under the age of 5 die from RSV each year).
Who knows if this data is true or not?
Speaking for myself, I haven’t forgotten how the Covid vaccine was pushed with the the extremely-dubious assertion that Covid was one of the “Top 8” killers of children.
I knew that statement was brazen disinformation because I’d researched actual children’s mortality from Covid while writing this story for uncoverDC.com.
In this article, I simply highlighted the key findings from the “most comprehensive” study of its kind on Covid mortality among children. The study, produced by a team of prestigious academics in the UK, found that only 25 children in the entire UK died “from” Covid in the fist year of the pandemic.
However, the headline that should have gone viral to parents across the world is that only six “healthy” children in the entire UK died “from” Covid.
Today, I’m going to revisit the findings of that study as this might cause a few mothers to question the pronouncements of our so-called public health experts, none of whom have seen a vaccine they don’t want every child to get, regardless of how unnecessary or what the long-term negative health effects might be.
The study’s key information and findings …
Approximately 12 million children (age 0 to 17) live in the UK.
The UK researchers were able to look at hospital diagnostic codes and find out how many children died “from” or “with” Covid in the first 12 months of the pandemic.
Here’s what study authors found and reported (CYP = “Children and Young Persons.”)
N = 61 – UK children who died in the first 12 months of the pandemic after testing positive via a PCR test.
Significantly, researchers subtracted 36 “Covid deaths” from this figure because they found these children actually died from some other cause. Language from the study:
“This is the first study to differentiate between CYP who have died of SARS-CoV-2 infection rather than died with a positive SARS-CoV-2 test as a coincidental finding. Our result is 60% lower than the figures derived from positive tests thereby markedly reducing the estimated number of CYP who are potentially at risk of death during this pandemic.”
N = 25 – UK children who actually died “from” Covid in the first 12 months of the pandemic.
But researchers looked even harder and found that 19 of these 25 Covid victims suffered from severe “life-limiting” medical conditions.
N = 19 = Children who died from Covid but had other major medical issues.
Subtracting the deaths of children who suffered from serious co-morbid conditions left researchers with …
N = 6 – “Healthy” children in the UK who died from Covid in the fist 12 months of the pandemic.
I made some additional assumptions/extrapolations …
To be very conservative, I assumed that 500,000 children (approximately 4 percent of the UK’s children) do suffer from serious “life-limiting” medical conditions (the real percentage is no doubt lower than 1 percent).
This would give us …
N = 11.5 million – Approximate number of “healthy” children in the UK.
We can now calculate the mortality risk for healthy children in the UK.
Covid Mortality Math: Six (6) Covid deaths divided by 11.5 million “healthy” children = Covid mortality of 0.000052 percent.
According to this extremely thorough (albeit ignored) study, the odds a healthy UK child would die from Covid in the first 12 months of the pandemic were 1-in-1.92 million. (Math: 11.5 million healthy children/6 Covid deaths).
I decided to do some politically-incorrect analysis …
To wander into politically incorrect territory, one can also calculate mortality risk by the race of children.
For some (undeniable) reason, Covid kills a much higher percentage of Blacks and Hispanics. This is true with children and adults.
Here’s a story from April 2020that proves that the disproportionate deaths among African Americans was already known (even though the authors of this article suggest that the CDC was already covering up these racial statistics).
The authors of the UK study also point out the racial differences in mortality rates:
“CYP >10 years, of Asian and Black ethnic backgrounds, and with co-morbidities were over-represented compared to other children.”
The authors also stressed that the absolute numbers of minority children who died from Covid was also minute. Still, the figures are strikingly minute for white children.
From further extrapolations, I concluded that only two, perhaps three, healthy white children in the entire United Kingdom died “from” Covid in the first 12 months of the pandemic.
Since there are more than 10 million healthy white children in the UK, I concluded the chance a healthy white child would die from Covid were approximately 1-in-5 million. As a percentage, this mortality risk is 0.00002. (One has to go out to the fifth decimal point to find a “risk” that is not zero.)
Why I did this research …
One reason I embarked on this research is that I was simply trying to ascertain accurate Covid information to inform any decision I made on whether my two young children should get the Covid vaccine.
I was doing my own research and did not automatically trust the proclamations of the CDC or the pediatrician groups. I know I’m not supposed to question my betters (the experts), but I did it anyway because my own children’s lives might be at stake.
I happen to be Caucasian, just like my two children. Thankfully our children are healthy and do not suffer from some terrible “life-limiting” medical condition.
Again, I was simply looking to find the mortality risk of my own two children if they didn’t get this “vaccine.” Thanks to this bold study, I found the answer I was seeking.
The data shows that my children might indeed die from Covid … but if they did they would be the one person in a cohort of 4,999,999 children who did.
To provide a little context, the odds a random person would get struck by lightning in a given year are about 1-in-750,000. The odds I might hit the lottery jackpot in neighboring Georgia are probably 1-in-3-million.
Anyway, you won’t be surprised to learn that I chose to not get my children vaccinated.
For me, becoming an “anti-vaxxer” was a no-brainer especially when I know the odds my children might contract potentially fatal myocarditis (or other serious vaccine injuries) might be as low as 1-in-3,000 (perhaps lower).
(The headline from the above-linked article notes that cases of myocarditis from vaccines are “rare” in children. If “rare” = a “1-in-3,000 risk,” how should one label a “1-in-5-million” risk?)
Even today, I occasionally read that the risks to children from Covid is “rare” or “small” or not as high as for, say, very old people or the morbidly obese.
But that’s poor word-smithing – intentionally so in my opinion.
When the risk of death for the largest population of children in America is 1-in-5 million, maybe journalists should consider more accurate risk modifiers, such as:
“virtually non-existent” … “almost unheard of” … “the rarest of anomalies” … “certainly nothing for parents to worry about” …. “for all practical purposes … zero.”
Anyway, when I kept reading that Covid was the “Top 8” killer of children in America, my go-to thought was, “That’s what they say.”
I guess the same pediatrician groups and the UK’s version of the CDC were spreading the same fear-mongering COVID disinformation as in America.
I’m sure Catherine, Princess of Wales was worried to death about getting her children vaccinated because she knew that Covid was one of the “top 8 killers of children in the UK.”
It probably never occurred to the princess to ask, “six deaths is enough to make the Top 8?” (Actually, I’d bet 100 pounds Princess Kate, just like 99 percent of UK mothers, never saw this study.)
I’m tempted to finish this column by saying, “none of this matters.” The narrative – as bogus as it was – worked as intended. Hundreds of millions of parents rushed out to get children vaccines they didn’t need.
Mass media is calling for the reinstitution of COVID restrictions due to new variants, with no conversation about the efficacy or the harm they’ve caused. Jefferey Jaxen connects all the dots, which appears to be pointing to a Pandemic 2.0.
Not only are you not unprotected due to natural immunity if you did not get the COVID injections, but the COVID injections were NOT vaccines. Therefore, you are also not ‘unvaccinated’ or an ‘antivaxxer’. Here are the reasons why the genetically engineered COVID injections were NOT vaccines:
A drug cannot be described as a vaccine until it is tested for a minimum of 10 years because many of the adverse health outcomes come out months and years later.
Question 1: How can a synthetic (man-made) drug be claimed to be ‘safe and effective’ or that the benefits far outweigh the risks, without this long-term data?
Question 2: Why did governments claim that it “would prevent people getting COVID disease” from the beginning of the roll out, when it was never tested in clinical trials, to see if it prevented COVID disease?
Welcome to the first Vaccination Decisions Substack. I have been writing newsletters for over a decade attempting to provide the knowledge that people need to understand the influence of the pharmaceutical companies and the UN’s World Health Organisation (WHO), in the Australian government’s decisions on public health policy.
This became necessary because the diversity of media ownership laws in Australia were removed over the last two decades, and this has led to a lack of independent vaccine information being provided to the general public.
Democracy only exists when the people can hold their government to account. This ability is removed once there is a lack of independence in the media. In Australia we have a corporate-sponsored media that is ~80% owned by Murdoch News Corp.
In this situation reality can be inverted as you have seen over the last three years: black becomes white due to the mis- and disinformation presented when governments collaborate with a corporate-sponsored media to control the information you receive. This is also described as public-private partnerships. Australia’s politicians are heavily influenced by corporate lobby groups, financial bonus’s and being required to present the government narrative through party policy.
Currently, the Australian government is attempting to further this censorship by pushing through new legislation in the Australian Communications and Media Authority (ACMA) Amendment (Mis and Disinformation) Bill 2023. This bill will allow the government to continue promoting the medical fraud that the UN/ WHO is directing (with financial incentives) to all member countries in global health policies.
There is a clause in this ACMA amendment bill that exempts politicians from being censored for the mis or disinformation that they provide on social media platforms. This legislation will completely remove the façade of democracy that still exists in Australia.
I have provided below a list of some of the false claims that governments and the medical-industry have made over the last three years that are now putting global populations at risk. It is time for everyone who has this knowledge to stand up visibly for the truth to ensure that ethics and principles can be restored to our society and institutions.
“If we lose courage we lose the truth and without the truth there is no other virtue” (Sir Walter Scott).
The False Claims Provided by Governments and the Medical industry in 2020-22:
Humans would not have any natural immunity to this new mutated Coronavirus 2019 (False). (The family of Coronaviruses cause the common cold, so the correct assumption is that we would have some naturalimmunity to a new mutation).
The PCR test can be used in people without symptoms to diagnose COVID disease (False). (It is a supportive tool and can only be used to assist in diagnosis when someone has symptoms. The PCR test is being misused and misinterpreted).
A healthy person can be diagnosed as an ‘asymptomatic case of disease’ using a PCR test (False). (A PCR test cannot be used to diagnose disease in people without symptoms: finding a virus in a person does not indicate they will ever get a disease because viruses only cause disease symptoms if there is a poor environment (terrain). A healthy person should never be classified as a ‘case of disease’ and isolated from society).
An ‘asymptomatic infection’ is a ‘case of disease and a ‘risk to the community’ (False). (This is an infection without symptoms and can only be identified with an antibody test (not a PCR test). A positive antibody test shows you have gained natural immunity to an infection without any disease symptoms. You are not a risk to others and healthy people should never be tested to see if they have a respiratory virus. There are hundred’s of viruses that cause ‘flu-like symptoms’.
Flus and colds disappeared in 2020-22 (False). (They were re-classified as a new disease called ‘COVID’ based only on a PCR test that was misused in healthy people. The diagnosis was not based on symptoms, or systematic testing for any other virus, bacteria or medication that cause the same symptoms).
These COVID mRNA injections are ‘vaccines’ (False). (They are genetically-engineered modified mRNA drugs until they are proven to prevent disease and that the benefits far outweigh the risks).
COVID ‘vaccines’ would prevent you getting COVID disease (False). (These genetically-engineered COVID injections were never tested to see if they prevent COVID disease and they are causing COVID disease.
Adverse events are ‘rare’ (False). (How can they be claimed to be ‘rare’ when the injections had not been studied in the genetically diverse population when they were marketed in 2021?).
The COVID ‘vaccines’ stimulate the immune system to produce a ‘Coronavirus spike protein’ (False). (They stimulate the immune system to produce a recombinant synthetic (man-made) protein that is foreign to our bodies and is being called a ‘spike protein’. This foreign protein can result in autoimmune diseases such as Multiple Sclerosis, Lupus, Chronic Fatigue Syndrome, Arthritis, Diabetes, Graves Disease, Guillain Barre Syndrome etc.
The book “Slaying the Virus and Vaccine Dragon” by John O’Sullivan et el, exposes the psychological strategies that were used by governments (directed by the WHO’s public-private partnerships) to predict and manipulate a global ‘pandemic’ based only on an industry-designed mathematical model that had hidden assumptions about viruses and vaccines. (Book Review).
References exposing these false government claims are:
Children’s Health Defense (CHD) will officially launch its “Vax-Unvax: The People’s Study” bus tour Friday in Olathe, Kansas. The 42-foot RV will travel across the continental U.S. over the next year, gathering stories of those who were harmed following vaccinations and COVID-19 countermeasures, including shots, masks, and medical and hospital protocols. The tour aims to provide a platform for the injured and survivors of loved ones who died — from parents and family members of the elderly to U.S. service members and veterans to the unvaccinated and others.
Leading the bus crew is CHD-TV Director of Programming Polly Tommey:
“We’re excited to be back on the road again and connecting with families around the nation who have important stories to tell regarding vaccine injury or risky medical agendas. We want to hear from everyone — vaccinated and unvaccinated — so we can learn about health outcomes firsthand from the people affected. While the mainstream media continues to ignore anything that goes against the Pharma/government mantra of ‘safe and effective,’ we will be here for everyone who wants to share their story.”
The kickoff comes as part of the two-day Freedom Revival in the Heartland event hosted by Kansans for Health Freedom. The bus crew will begin filming interviews at 9 a.m. on Friday, collecting the names of the injured and of those who have passed by writing them on the outside of the bus in tribute.
Speakers at the Freedom Revival in the Heartland event include CHD Chairman on leave Robert F. Kennedy Jr. and CHD Chief Scientific Officer Brian Hooker, Ph.D. — co-authors of the upcoming book “Vax-Unvax: Let the Science Speak” to be released on Aug. 29. The bus tour coincides with the book, which is a compendium of over 100 vaccinated-unvaccinated studies comparing health outcomes in both populations, with nearly all indexed in PubMed, the National Library of Medicine’s vast database of biomedical scholarly research. Tommey and CHD President Mary Holland are also speaking at the event.
Visit CHD’s website for more information on the ‘Vax-Unvax: The People’s Study’ bus tour, including scheduled stops around the country.
Children’s Health Defense® is a 501(c)(3) non-profit organization. Our mission is to end childhood health epidemics by working aggressively to eliminate harmful exposures, hold those responsible accountable and establish safeguards to prevent future harm. We fight corruption, mass surveillance and censorship that put profits before people as well as advocate for worldwide rights to health freedom and bodily autonomy.
The Kaiser Family Foundation is a pro-vaccine organization that has an biased polling system aimed at showing satisfaction and benefit of mass vaccination among other family issues. The May 23 through June 12, 2023 poll reveals some shocking new data. A substantial minority of Americans believe the COVID-19 vaccines have caused great harm. Here are the results.
As you can see it is roughly a third of Americans are awake and understand the COVID-19 vaccines have failed, cause great harm, and pose a giant safety risk to Americans. It is also interesting to note a quarter of respondents have been awakened to the link between childhood hyper vaccination and autism spectrum disorder. I wonder what the actual sentiment is on vaccines if Kaiser had asked the questions in a more unbiased manner and did not load up their survey with charged words such as “false” and “misinformation”.
The Journal of the American Medical Associationrecently published a review of alleged ‘misinformation’ about COVID-19 that physicians were responsible for, either on social media and in other news sources.
In the paper, the corresponding author, Dr. Sarah L. Goff, MD PhD, defined misinformation. She surveyed social media platforms and news sources for anything written by other physicians that fits her selected examples of both. She then proposes that physicians guilty of writing what she judges to be misinformation should be “regulated and disciplined”.
Dr. Goff and her co-authors define misinformation as “false, inaccurate or misleading information according to the best evidence available at the time” and disinformation as “having an intentionally malicious purpose”.
Dr. Goff states: “We conservatively classified inaccurate information as misinformation rather than disinformation because the intent of the propagator cannot be objectively assessed.”
Dr. Goff identified four major themes of alleged misinformation. These included: (1) vaccines were unsafe and/or ineffective; (2) masks and/or social distancing did not decrease risk for contracting COVID-19; (3) other medications for prevention or treatment were effective despite not having completed clinical trials or having been FDA approved, and (4) other misinformation.
Dr. Goff includes a brief discussion of vaccine safety and effectiveness and mask effectiveness, but does not attempt to undertake a full review of the published evidence in these areas. Instead, she seems to assume that her readers will agree that any suggestion that vaccines or masks were ineffective or unsafe are self-evidently false.
Dr. Goff states that the American Medical Association has called for disciplinary action for physicians propagating COVID-19 misinformation. She laments the fact that “few physicians appear to have faced disciplinary action” for alleged sins against Covid orthodoxy.
I am not an expert in analysis of published medical research. I don’t work in a School of Public Health like Dr. Goff. I have worked as a licensed physician in England for over 40 years as a family doctor and an occupational physician and I have over 40 years’ experience reading the medical peer review literature. I retired from full time medical practice in 2017. I have a reasonable understanding of English, maths, logic and critical thinking. I don’t pretend to have read all the published research on masks or vaccinations. However, I continue to read leading medical journals on a regular basis.
I understand the concept of truth and how hard it is to establish an absolute truth in science. I understand the enlightenment principles that any ideas can be discussed, that nobody has a veto on ideas and that it is important to doubt and test all of our ideas continually. There is no indication from her writing that Dr. Goff understands how important it is to doubt, question and test the effectiveness and safety of interventions such as vaccines and masks.
From my reading of the peer review literature, for illustration purposes, I identified the following four publications as examples of publications which should raise concerns and questions about COVID-19 vaccines and masks.
In February 2023 a Cochrane review into the effectiveness of masks concluded: “Compared with wearing no mask in the community studies only, wearing a mask may make little to no difference in how many people caught a flu-like illness/Covid-like illness.”
A study from the University of Queensland in September 2022 concluded: “Never in vaccine history have 57 leading scientists and policy experts released a report questioning the safety and efficacy of a vaccine. They not only questioned the safety of the current COVID-19 injections but were calling for an immediate end to all vaccination. Many doctors and scientists around the world have voiced similar misgivings and warned of consequences due to long-term side effects.”
These four publications are examples which give us a legitimate reason to question the use of masks and the Covid vaccines and to look further for evidence. Are we not allowed to raise questions about these issues without being threatened with disciplinary procedures? Not to ask any questions would be lacking in curiosity in the extreme, especially for practising physicians concerned about the safety of their patients and the integrity of their advice. These publications do not prove anything conclusively, but they should not be ignored. Expressing doubt and asking questions about the safety and effectiveness of vaccines and masks is not false, inaccurate or misleading, to use the definition adopted by Dr. Goff. If questions arise in my mind, why don’t similar questions arise in the minds of Dr. Goff and her co-authors? How did Dr. Goff reach such a degree of certainty about the effectiveness of masks and vaccines against COVID-19 that she can classify any statement to the contrary as misinformation worthy of disciplining a colleague? Why does she conclude that a colleague who disagrees with her does not have the right to be heard? Why would she seek to silence those who disagree with her?
Inaccurate information which is not deliberately intended to deceive is simply inaccurate. In science and medicine there are many inaccurate statements made in good faith by researchers who are presenting their data or their theories as accurately and honestly as possible. It is important that all theories and all research data can be published, even when the data or the theory are wrong. Disciplinary action for any statement which turns out to be inaccurate or false would surely suppress a large proportion of all scientific and medical discourse. Is this what Dr. Goff wants?
It could be argued that the examples of misinformation used by Dr. Goff are themselves misinformation. To suggest that anyone who states that the Covid vaccines were unsafe and/or ineffective is guilty of misinformation is to ignore significant evidence which raises questions about the vaccines. To suggest that anyone who states that masks did not decrease risk for contracting COVID-19 is guilty of misinformation is also to ignore evidence to support this view. It could be argued that Dr. Goff is using false, inaccurate or misleading examples of misinformation in her study in order to suppress dissenting views.
Dr. Goff appears to have very little humility. She does not appear to be in any doubt that she and her co-authors are infallible in relation to masks and vaccines. She seems to think she is the ultimate arbiter of truth, and that she is immune from being regulated or disciplined for her views in the way she promotes for others. I would not propose disciplining or applying regulatory sanctions to Dr. Goff or her colleagues if her publication includes false, inaccurate or misleading statements. Instead, I would propose respectful dialogue with her to debate her proposal, offering arguments to the contrary with a view to educating her and myself.
In England, medical doctors are obliged to respect colleagues’ skills and contributions, and to treat colleagues fairly. We must create a working environment in which it is safe to ask questions and raise concerns. I believe in these principles. Failure to adhere to these standards can lead to disciplinary action against medical doctors. I understand that similar professional obligations apply to medical doctors in the United States. Dr. Goff does not appear to respect the skills and contributions of colleagues who disagree with her. She seems to be promoting a working environment in which it is not safe for those who disagree with whatever the orthodoxy within the medical profession is at any one time to ask questions and raise concerns. Does she not realise that this may make it unsafe for her to raise concerns and ask questions in due course?
Dr. Goff acknowledges in her final sentence that “a coordinated response by federal and state governments and the profession that takes free speech carefully into account is needed”. This tiny nod towards free speech is somewhat undermined by her attempts to censor her colleagues’ right to disagree with her. Free speech is nothing if it is not accorded to those with whom we disagree.
Frederick Douglass, the American social reformer said: “To suppress free speech is a double wrong. It violates the rights of the hearer as well as those of the speaker.” If Dr. Goff persuades those in power to regulate or discipline those who disagree with her, then their right to free speech is violated and our right to hear them is violated. Does Dr. Goff not have a glimmer of doubt about her omniscience? Does she not think there is even a faint possibility that physicians who disagree with her might have something useful to say?
Why do some physicians think that the best response when another physician disagrees with them is to censor their colleague? How could any physicians achieve such unshakeable certainty in their own omniscience? When did they forget the fundamental principles of the enlightenment, that all ideas can be discussed and that nobody has a veto on any ideas? How did the principles of treating colleagues with respect and upholding the free speech of those with whom we disagree become so degraded?
Dr. Goff and her co-authors should be careful what they wish for. They seek to discipline colleagues for daring to disagree with their orthodoxy. If they succeed, the cancel police may be coming for them next.
Dr. Nigel Wilson MRCGP FFOMis a retired consultant occupational physician.
The Centers for Disease Control and Prevention (CDC) V-safe website quietly stopped collecting adverse event reports with no reason or explanation. The V-safe website simply states: “Thank you for your participation. Data collection for COVID-19 vaccines concluded on June 30, 2023.” If you go there today, V-safe directs users to the FDA’s VAERS website for adverse event reporting, even though officials continually derided VAERS as “passive” and “unverified.”
VAERS and V-safe are mutually exclusive safety collection databases operated by the FDA and CDC, respectively. VAERS is an older way of collecting safety data where one can fill out a form online, or manually, or by calling a toll-free number, whereas V-safe is a device “app” which requires online registration. Both VAERS and V-safe collect personal information, lot numbers, dates and associated information, but V-safe was an active collection system geared towards a younger app-using demographic.
Does this mean that the CDC believes that the mRNA Covid-19 injections are so safe, there is no need to monitor adverse event reports any longer? What is the argument against continued monitoring, especially since the V-safe website was already up and paid for?
While CDC’s V-safe was stealthily and abruptly turned off, refusing to accept new safety reports, to this very day the CDC continues to urge everyone ages 6 months and older to stay up to date with COVID-19 vaccines and boosters.
As a drug safety expert, I personally can’t cite another example of any agency or manufacturer halting collection of safety data. It seems even worse because mRNA technology is relatively new with long-term manifestations unknown. On top of this, both manufacturers and the FDA refuse to sharethe list of ingredients, such as lipid nanoparticles, which could affect individuals differently and take a long time to manifest clinically.
Safety Data Collection Should Never Stop:
Now, contrast that with the fact that the National Highway Traffic and Safety Administration (NHTSA) will still accept a safety report for a 30-year-old Ford Bronco II. Indeed, this is an oddly specific example, but only because I drove this exact vehicle as a family hand-me-down as a student, through my residency, fellowship, for my tenure as a Yale professor on the mean streets of New Haven and even during my years at the FDA as a medical officer /senior medical analyst.
Like mRNA shots, Bronco IIs are still available on the market and people are still using them up to this very day. My Bronco became an intermittent topic of conversation with friends and FDA colleagues. One day, I was informed by a patrolling security guard at the FDA that it was the oldest car on campus.
I didn’t know much about cars (or mRNA technology) back then, but when a fellow FDA-er informed me that my Bronco II had noteworthy safety problems and that the NHTSA still had their eye on this vehicle (rollover accidents were more common and more fatal) I addressed the problem: I got rid of the reliable relic, even though I reallyliked it. NHTSA Is still accepting safety reports three decades later.
Interestingly, the NHTSA link above on my Ford Bronco II only shows: one parts recall, one investigation and 23 complaints, and still features a button in the upper right hand corner for submitting new complaints.
Wikipedia defines an humanitarian crisis or humanitarian disaster as a: “singular event or a series of events that are threatening in terms of health, safety or well-being of a community or large group of people.” Based on VAERS and previous V-safe findings, adverse events from mRNA shots in the USA alone could be considered a humanitarian crisis.
Despite those alarming clinical findings, the CDC has concluded that collecting new safety reports is somehow no longer in the interest of America’s public health. Existing data from the V-safe site showed around 6.5 million adverse events/health impacts out of 10.1 million users, with around 2 million of those people unable to conduct normal activities of daily living or needing medical care, according to a third-party rendering of its findings. In other words, despite mRNA shots still being widely available and the CDC promoting its continued use, it’s “case closed” with regards to collecting new safety reports, under today’s federal public health administration.
Will the CDC opine on the existing data or justify its halting of collecting new safety data? To the best of my knowledge, stopping the collection of public health information doesn’t have a clinical justification or scientific precedence — especially when it comes to an actively marketed product.
In George Orwell’s 1984, characters were told by The Party to “reject the evidence of your eyes and [your] ears.” Now, the CDC isn’t even allowing that evidence to be collected for viewing (and prospective rejecting). It’s a terrible idea for any product, let alone novel mRNA technologies.
Dr. David Gortler, a 2023 Brownstone Fellow, is a pharmacologist, pharmacist, research scientist and a former member of the FDA Senior Executive Leadership Team who served as senior advisor to the FDA Commissioner on matters of: FDA regulatory affairs, drug safety and FDA science policy. He is a former Yale University and Georgetown University didactic professor of pharmacology and biotechnology, with over a decade of academic pedagogy and bench research, as part of his nearly two decades of experience in drug development. He also serves as a scholar at the Ethics and Public Policy Center.
The ABIM’s history proves their present actions are political/financial and not scientific. They are making examples of us “dissenters” to scare the rest of the country’s docs to keep quiet.
The unholy alliance of industrycaptured high-impact medical journals, federal public health agencies, professional societies (ABIM, AMA, APHa etc), and most importantly, the state medical licensing boards directed by the Federation of State Medical Boards (FSMB) are still going hard after us “dissenting” doctors. You know, those of us that very publicly called out the unscientific policies implemented by corrupted policymakers in a directed pursuit of profits and power. Their actions trying to silence us (and to scare other doctors from speaking out) are escalating.
Recently, what I call the “misinformation committee” of the American Board of Internal Medicine (ABIM) voted to strip Professor Paul Marik and myself of our Board certifications. To best understand why they would do this, I think it is important to review what the ABIM is, how it operates, and then detail their absurd attempt to paint us as misinformationists by using disinformation.
Let’s trace my current relationship with the ABIM to today:
At the end of my training, I became Board Certified by the ABIM in three specialties (Internal Medicine, Pulmonary Diseases, and Critical Care Medicine).
What is the ABIM? Well, from this devastating article by Kurt Eichenwald, an accomplished corporate investigative journalist who did a devastating takedown of the ABIM and its officers in a Newsweek piece in 2015:
The ABIM is a purported nonprofit that certifies new physicians as meeting standards of practice. Beginning in the early 1990s, the ABIM ordered certified doctors to be recertified, again and again. Without the ABIM seal of approval, lots of internists and subspecialists can’t get jobs and can’t admit patients to hospitals. So by taking advantage of that monopolistic power, the ABIM has forced hundreds of thousands of physicians to follow recertification processes that doctors complain cost them tons of money (paid to the ABIM), require tons of time (taken from families and medical practices) and accomplish nothing.
In many doctor’s opinion, this cash grab of the ABIM by selling “certifications” is a corrupt farce. There is no evidence that certifying doctors in this highly costly way does anything to improve the quality of care delivered. The ABIM has not only refused to produce data showing the program improves patient care but also hasn’t conducted any studies on that matter. In fact, the ABIM and its related organizations are:
harming American medicine and diminishing the quality of scientific research, pushing physicians to close practices rather than wasting time on expensive and frustrating busywork, and forcing specialists to play a game of medical trivial pursuit. (Even Baron has admitted that he was tested for recertification on topics he never used in his practice.)
But it sure does generate cash for ABIM executives. Note that Board Certification used to simply be a sort of “honor” denoting that the member passed a more rigorous examination in their specialty. That “honor” comes at a price though:
Since I am (was?) Board certified in 3 specialties, lets do some math as this is what it costs me to re-certify every ten years:
$1,430 for Internal Medicine
$2,325 for Pulmonary Diseases
$2,325 for Critical Care Medicine
But wait, we are not done yet. These bastards were not making enough money with once-every-ten-year recertification exam fees, so they invented a new program of annual busywork education requirements which they called Maintenance of Certification (MOC) which costs you $220 every year for every certification (plus late fees if you forget). To wit, I went into my patient portal and discovered. I owe them $480 for each of my certifications!
And get this – that money essentially goes to ABIM executive salaries and pensions and other dubious private investments as described by Eichenwald where he details the insane lengths the ABIM goes to “hide” the compensation and pension data on its executives. What is worse is that ABIM certification has now been made a requirement of employment as a faculty member of academic medical centers and hospitals and is also a requirement to be on many insurance company panels (these actions further strengthen the control of doctor behavior).
Doctors have started publicly slamming the group in industry publications. “ABIM is imposing on us an onerous and ill-conceived tool, one that most physicians agree is irrelevant,” Dr. Karmela Chan wrote in Internal Medicine News. “I am glad this conversation is happening, because, frankly, the process was enough to make me want to quit being a doctor.” Further, in a recent poll of 2,211 physicians conducted on a doctors-only website called Sermo, 97 percent of the respondents criticized recertification.
Richard J. Baron, the ABIM CEO that sent letters threatening decertification to me and Paul, makes close to a million dollars a year, however that data is almost impossible to find due to the ABIM’s multiple attempts to obscure it as well as its spokespeople avoiding answering any inquiries on the topic. Here is a summary of Eichenwalds findings on the ABIM:
In 2015, they were 5 months late in filing their publicly available financial report with the IRS (that several journalists were very interested in).
The report is full of obfuscations and anomalies of reporting of not only the actual money earned by the executives, and particularly Baron, but his financial conflicts of interest are even better hidden.
A big percentage of the ABIM’s millions was in the form of cash to one former employee.
The ABIM in 2013 had 57 million against liabilities of 105 million – while Baron was going around saying that its assets are three times its liabilities (this was a 100% lie. When I get to the ABIM’s response to our defense letter, remember that what liars do is.. lie).
It lost $4.8 million on $55.5 million in revenues, no small feat and almost entirely due to a bloated payroll.
It also claims it spends no money on lobbying while it spent between 100K to 160K annually to lobby Congress on Medicare and Medicaid (another lie).
The data on top officers compensation is so obscured and fragmented, Eichenwald reported that he had found it much easier to discover executive compensation at Enron, Worldcom and Adelphia – all famous for lying on tax filings. Again no small feat (to be one of the top corporate liars in the U.S).
Officers “double dip” – former CEO Christine Cassel got $741K from ABIM and $247K from the ABIM “Foundation” (slush fund for ABIM officials) and also got $219K in “other compensation” – totaling $1.2 million for one year. (Nice gig if you can get it).
But wait, we are not done. Cassel also got $504K in “deferred compensation” for a total of $1.71 million more that year (six times the median compensation for similar sized non-profits). Six times.
Then there is this doozy of an article which came out this week in The Defender by Children’s Health Defense, detailing the ABIM CEO Richard Baron’s conflicts of interest:
Some of the most disturbing reveals:
“The head of a national medical organization who publicly called for doctors to lose their licenses unless they supported government narratives on COVID-19 treatments and vaccines concealed his relationship with a public relations firm whose client list also included Pfizer, Moderna and the Centers for Disease Control and Prevention (CDC).
Dr. Richard Baron, president and CEO of the American Board of Internal Medicine (ABIM) is a client of Weber Shandwick, investigative journalist Paul D. Thacker reported on Wednesday.
Note that I went after Weber Shandwick in my book, “The War on Ivermectin” where I argue (without proof, although I believe that is coming because I know of a subpoena coming their way) that they created and launched the “Horse Dewormer PR campaign,” highlights of which was the famous FDA tweet and absurd Rolling Stone article:
In late 2021, Baron publicly pushed for doctors who spread “misinformation” about COVID-19 and the vaccines to lose their license and certification.
According to Thacker, “Weber Shandwick’s panel featuring Dr. Baron has been widely promoted by the PR firm’s employees,” including Sarah Mahoney, executive vice president, Healthcare Communications, Strategy & Planning for Weber Shandwick, who in a LinkedIn post, wrote she “can’t think of a more important topic right now.”
Although to the unawake the following may seem normal public health practice, but to those of us fighting agency capture by Big Pharma, it is absurd:
The CDC’s National Center for Immunization and Respiratory Diseases (NCIRD) in September 2020 awarded Weber a $50 million contract “to promote the vaccination of children, pregnant women and those at risk for flu and increase the general acceptance and use of vaccines,” according to the PR firm’s website.
Thacker said he believes much of what is labeled “misinformation” in medicine and academic research “is really just corporate PR,” and that “Congress needs to take a harder look at funding for ‘misinformation research.’“
Speaking of taking a harder look at where the funding is coming from for “misinformation research” and the ABIM, it turns out that.. we can’t. Why? Check out this tweet showing a clause inserted into the ABIM’s by-laws in 1998:
But wait, it gets better, like way better. Also in their by-laws:
Information that is disclosed will be kept confidential except to the:
President and Chair of the Board;
The chairs of the relevant Subspecialty Boards, Test-Writing Committees, and other Committees of the Board, members who serve on the relevant Boards and Committees, and staff working with the respective committees;
The Conflict of Interest Committee members and Conflict of Interest Committee staff,
except as required for the purposes of continuing medical education.
So, basically, they can take money from any corporate entity and do not have to disclose it to anyone. Again, nice gig if you can get it.
Back to the ABIM’s history: One of Eichenwalds more disturbing observations about the behavior of the ABIM:
I can attest to the ABIM’s pomposity. Starting with my first story about the ABIM, the organization usually has refused to acknowledge I even asked a question. The only other group to do that in my 30-year journalism career was a company that processed payments for child pornography websites. Plus, when I reported on the uprising by doctors, the ABIM ignored the facts and instead investigated me.
Now lets fast forward to Covid. On July 29, 2021, the FSMB (this entity controls the state medical licensing boards, not the ABIM – at least on paper) issueda policy statement that “Physicians who generate and spread COVID-19 vaccine misinformation or disinformation are risking disciplinary action by state medical boards, including the suspension or revocation of their medical license.”
What is interesting is how fast and how rigidly the ABIM followed the FSMB’s lead and enacted their own misinformation policy despite the fact that, as my colleague Meryl Nass has pointed out:
“suddenly claiming that using licensed drugs for COVID, criticizing federal policies for COVID or criticizing the value of COVID vaccines is unprofessional” gives the specialty board the right to revoke a certification—well, that was never part of its contract with me.So pulling my certification for issues that were never specified in the original contract is breach of contract.
I think it would only be a breach if contracts, like our Constitution and the practice of medical ethics, were still “a thing.”
The ABIM apparently liked the FSMB’s “misinformation policy” idea to attack dissenting doctors so much (or were told to like it) that 2 months later, they,along with their colleagues at the American Board of Pediatrics and the American Board of Family Medicine, issued a statement supporting the FSMB’s position, saying, “We all look to board certified physicians to provide outstanding care and guidance; providing misinformation about a lethal disease is unethical, unprofessional and dangerous.” (note that they seem particularly focused on Covid misinformation and not any other disease model or therapeutics. Do you think it could be because Covid vaccines and therapeutics opened immensely profitable markets to Pharma overnight?).
Again from Meryl Nass (please subscribe to her Substack):
Furthermore, the processes the ABIM is using, as described by CEO Richard Baron, MD in his podcast with the New England Journal of Medicine are procedurally unfair. Dr. Baron earns $1 million/year to threaten doctors for a crime that does not exist. Baron, notably, refused to specify where the line was between misinformation and genuine disagreement in that podcast, though he seems to have no difficulty at all drawing the line when it comes to licensees who speak publicly about how to manage COVID. In a truly Orwellian effort, the ABIM and the ABIM Foundation have dedicated the year to ‘building trust’ in medicine.”
In what I suspect was the ABIM’s first enforcement of their shiny new policy, they go after Peter McCullough, Paul Marik, and myself on the same day (May 26, 2022) with a letter quoting numerous public statements we made, implying that we needed to defend the substance of such statements with supporting data or risk losing our certifications.
“Game on” I thought, looking forward to the exercise of “debating” scientific data with the ABIM. However, our FLCCC lawyer, Alan Dumoff pointed out that the ABIM’s policy and procedures state that the process of accusing a member of misinformation requires that they first provide evidence to us that what we said was inaccurate. So, we wrote back, pointing out to the ABIM their brazen “error” (yeah right) in not complying with their own policy and procedures.
“Nonsense” they wrote back (in short). Their logic was truly shocking – they say that the fact they provided the substance and references to my public statements means they did their duty (rather than their providing references that would refute my statements which is what their policy states they need to do).
You can read their brazen, illegitimate, dismissive response here:
This letter above demonstrates the unchecked power they have – they alone determine whether they are following their own policy which they so clearly were not. What did I say about liars before?
Anyway, rebut them we did. We wrote a 76 page treatise with 175 references, 11 exhibits, and 22,000 words, marshaling and weaving numerous data sources to support all our public statements that they had a problem with. May it enter the historical record here (I think you Covid vaccine and ivermectin data geeks will find the letter impressive).
We sent that letter over 6 months ago… and finally got an answer a few weeks ago. To understand the misinformation committee’s response, note this statement from an editorial written by Baron where he tries to give examples of misinformation:
A whole range of statements with which many — or even most —physicians might disagree would therefore not trigger our disciplinary process. On the other hand, when someone certified by the ABIM says something like “the origin of all coronary heart disease is a clearly reversible arterial scurvy” or “children can’t spread Covid” or “vaccines don’t prevent Covid deaths or hospitalizations,” we are not dealing with valid professional disagreement; we are dealing with wrong answers.
That last sentence is critical as Baron literally is saying that the ABIM gets to determine what is a valid professional disagreement versus a “wrong answer.” Good to know, especially in regards to the fact that the narrative that “vaccines prevent Covid deaths or hospitalizations” was strongly refuted in our initial response letter.
This issue about drawing a line between misinformation and genuine disagreement is a critical one. From our letter of appeal written by our lawyer Alan Dumoff:
Threshold Issue: What Standard Distinguishes Legitimate Differences of Professional Opinion and Misinformation
We disagree with the Committee’ s interpretation of the data, which we address below, but the initial question is by what standard the American Board of Internal Medicine (“ABIM” or “Board”) evaluates evidence to determine that disagreement with consensus generally, and regarding controversial matters around COVID-19 policy specifically, rise to the level of actionable misinformation. The Board’s policy recognizes the right to legitimate debate, which requires it not merely show evidence supporting a consensus view but that it demonstrate that these professional disagreements are not legitimate but outright misinformation.
If not grounded in an articulated standard, at the very least, the Board must demonstrate that the views at issue are false by citing the fallacies in the actual substance of the evidence provided, not simply by critiquing a few isolated studies divorced from the totality of evidence. Resting solely upon citations to mainstream publications while substantially avoiding the evidence in our Submission, and our detailed critiques of these publications does not provide a basis for the Board to take action against my clients.
A diplomate’s medical positions must be plainly erroneous to merit sanction. Departure from consensus is hardly unusual and by itself insufficient. While the Sanctions Notice gives the appearance of having done so, the Committee did not directly engage the numerous imperfections in the mainstream approach Drs. Kory and Marik’s have pointed to in substantial detail. The Committee has not engaged the evidence submitted and demonstrated it is illegitimate, only that it departs from the consensus, that is insufficient to support a sanction.
The point is that the ABIM appears absurdly obsessed with getting doctors to spout only consensus opinions. This is literally unprecedented in science. From Michael Chrichton the author:
I want to pause here and talk about this notion of consensus, and the rise of what has been called consensus science. I regard consensus science as an extremely pernicious development that ought to be stopped cold in its tracks. Historically, the claim of consensus has been the first refuge of scoundrels; it is a way to avoid debate by claiming that the matter is already settled. Whenever you hear the consensus of scientists agrees on something or other, reach for your wallet, because you’re being had. Let’s be clear: the work of science has nothing whatever to do with consensus. Consensus is the business of politics. Science, on the contrary, requires only one investigator who happens to be right, which means that he or she has results that are verifiable by reference to the real world. In science consensus is irrelevant. What is relevant is reproducible results. The greatest scientists in history are great precisely because they broke with the consensus. There is no such thing as consensus science. If it’s consensus, it isn’t science. If it’s science, it isn’t consensus. Period.
I love that last line so much it bears repeating, “If it’s consensus, it isn’t science. If it’s science, it isn’t consensus. Period.”
Now, let’s look at their response to our 76 page letter teeming with supportive data for our statements. Can read their letter in its entirety here but I thought I would just pull the most illustrative sections:
… the CCC (i.e. misinformation committee) concluded that your statements about the purported dangers of, or lack of justification for, COVID-19 vaccines are false and inaccurate because they, too, are not supported by factual, scientifically grounded, and consensus driven scientific evidence. In fact, the overwhelming body of factual, scientifically grounded, and consensus-driven evidence – at and since the time you made those statements – shows that the COVID-19 vaccines are safe and effective for children and for adults
I have heard of the term “evidence-based medicine (EBM)” which is what I practice, but not “consensus driven science” (completely new invention – pernicious indeed. I Actually adhere to the original definition and conceptual framework envisioned by the founders of evidence based medicine which was incredibly well detailed in a by my friend “A Midwestern Doctor” in his brilliant recent post “What Happens To Doctors Who Innovate”.
Anyway, they then listed a few published, peer-reviewed papers supporting their point, blissfully un-acknowledging of the fact that the high-impact journals have been systematically censoring pretty much all negative analyses of the vaccine campaign’s impacts while publishing nothing but positive reports with cherry-picked and/or fraudulent data – so there is no way for the truth about vaccines to win in scientific debates my friends.
The high-impact journal censoring of adverse vaccine data is identical to their censoring of dozens of positive trials of ivermectin, something I extensively detail in the chapter called “The Journal Rejections of Positive Ivermectin Studies” in my book.
It gets even better – they next argue against my claims of lack of safety of the vaccines by, get this, referencing proclamations by the WHO and CDC. They ignore all the immense data to the contrary that I submitted while of course being willfully oblivious to the fact that the CDC and WHO are fully Pharma captured agencies:
Moreover, the vaccine safety data overwhelmingly (overwhelmingly?) contradicts your statements about vaccine risks. See, e.g., Centers for Disease Control and Prevention, “Safety of COVID-19 Vaccines,” https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/safety-of-vaccines.html (updated March 7, 2023) (reporting that “Adverse Events (Serious Safety Problems) Are Rare,” and that “[t]he benefits of COVID-19 vaccination outweigh the known and potential risks”); World Health Organization, “Safety of COVID-19 Vaccines,” https://www.who.int/news-room/feature-stories/detail/safety-of-covid-19-vaccines (March 31, 2021) (stating that “[b]illions of people have been safely vaccinated against COVID-19,” that “mRNA vaccines [for COVID-19] have been rigorously assessed for safety, and clinical trials have shown that they provide a long-lasting immune response”).
The paragraph above should enter the historical record… somewhere. That will NOT age well. The only thing more absurd to contemplate is whether they know they are lying in their letter or if they are simply referencing propaganda that they themselves swallowed whole? In a way, the former might be more acceptable to me at this point.
Their opinion on how I got ivermectin wrong was similarly brazen – they ignored all the meta-analyses (historically considered the strongest form of data, a fact they seem to have willfully avoided) in favor of listing a handful of trials where ivermectin was supposedly found ineffective, relying mostly on citing “the Big 6” (what I named the chapter describing the fraud behind the 6 largest, Pharma-conflicted and most publicized trials on ivermectin). This was 100% unsurprising.
Check it out:
First, the CCC concluded that your statements about the safety and efficacy of ivermectin and hydroxychloroquine as treatments for COVID-19 are false and inaccurate because they are not supported by factual, scientifically grounded, and consensus driven scientific evidence (there it is again).
Susanna Naggie, M.D., M.H.S., et al., “Effect of Ivermectin vs Placebo on Time to Sustained Recovery in Outpatients With Mild to Moderate COVID-19,” 328 JAMA 1721 (2022), https://www.nejm.org/doi/full/10.1056/nejmoa2115869 (finding in a double-blind, randomized, placebo-controlled study with 1,800 participants that “[a]mong outpatients with mild to moderate COVID-19, treatment with ivermectin, compared with placebo, did not significantly improve time to recovery,” and that “[t]hese findings do not support the use of ivermectin in patients with mild to moderate COVID-19”);
I laughed out loud when they led their argument with the Naggie trial funded by the NIH as it contained the most brazen fraud of the Big 6 Pharma Ivermectin trials. All you need to know about the trial is that they moved the primary comparison endpoint of the trial.. in the middle of the trial. They moved the main comparison from symptoms at Day 14 to Day 28. Note that changing endpoints in the middle of a trial is a supposed never event. Except the same trick was pulled in the Remdesivir trial.
Anyway, in a presentation by Naggie, in this secondary endpoint, you can see that ivermectin was superior at Day 14 to a high degree of Bayesian “statistical significance” but the “statistical significance” was not reached at Day 28 (I use quotes around statistical significance because it is an erroneous concept when doing Bayesian statistics but that is what they did anyway when they pre-specified a threshold of above 0.95 as “significant”). Can anyone tell me why they moved the endpoint to Day 28 in the middle of the trial:
With this brazen maneuver (and many others) it allowed Naggie et al to publish this conclusion: “these findings do not support the use of ivermectin in patients with mild to moderate COVID-19.” Not-so-fun fact: Naggie also sat on the NIH covid treatment guidelines committee where she voted to not recommend ivermectin right before she and her University received tens of millions.. to study ivermectin in Covid. You want more? She also owns stock in a competitor to ivermectin (monoclonal antibodies for Omicron) and has received money from numerous other Big Pharma companies including Gilead. Lets get back to the letter…
Rather, the CCC seeks to accomplish precisely what you assert ABIM should be doing: seeking to “further the professional integrity of medicine by encouraging evidence-based debate” (emphasis added).
Indeed, as set forth in ABIM’s False or Inaccurate Medical Information policy, physicians have an ethical and professional responsibility to provide factual, scientifically grounded, and consensus driven scientific evidence (there it is again). As discussed above, by touting the effectiveness of ivermectin and hydroxychloroquine as COVID-19 treatments and casting doubt on the efficacy and safety of COVID-19 vaccines with such seemingly authoritative statements, you have made statements that are inimical to ABIM’s ethics and professionalism standards for board certification.
In light of all the evidence and circumstances, the CCC determined to recommend that your board certification be revoked.
There is only one silver lining here. One – the impending loss of my certifications does not affect me materially because I have a private fee-based practice due to my need for complete autonomy and lack of restrictions in empirically treating the vaccine injured with various repurposed and alternative therapeutics. I thus cannot and will not accept insurance, and secondly, my academic career is over – no longer will I ever enter back into the system of medicine.
About the only opportunity this whole attack has created is one where I get to defend myself on appeal in a debate with three academic white coats of their choosing. Bring. It. On.
Although the outcome of the debate is assuredly pre-determined, I know it will satisfy a deep yearning many of us dissidents have had for going on 3 years now – to debate someone, anyone, anywhere. Crush them with data. Make ‘em look silly although I will be the only one who knows it happened. It will let me vent my disgust at how they have widely disseminated corrupted scientific evidence and policies while simultaneously ignoring the clinical observations and expertise of frontline doctors who have treated thousands of actual Covid patients.
I will then toss in a little lecture about how RCT’s have long ceased to be a credible means of proving anything in science given that in modern medicine only “Big RCT’s” count and that all “Big RCT’s” require such massive funding that the bias of the funders outweighs any objectivity such trials can profess to attain. I will also remind them that throughout modern medical history, the findings of RCT’s and retrospective observational trials are identical, yet academia has been taught to systematically ignore observational trials. Reason: only massively funded entities can conduct a “Big RCT” while any committed clinician willing to give up nights and weekends can conduct an observational trial. Pharma cannot allow research to be conducted that they have no control over – so they took over the journals and medical school curriculums which now literally teach that observational controlled trials can only be considered “hypothesis generating” and thus their results should not be acted on. Nonsense.
I will also remind them that they are violating international law and human, civil, and political rights as argued by Meryl Nass in another of her excellent posts regarding her own persecution by her state licensing Board:
International law is on our side. A total of 172 countries are parties to the International Covenant on Civil and Political Rights:
According to the 1948 Universal Declaration of Human Rights, Article 19,
“Everyone has the right to freedom of opinion and expression; this right includes freedom to hold opinions without interference and to seek, receive and impart information and ideas through any media and regardless of frontiers.”
“Everyone shall have the right to freedom of expression; this right shall include freedom to seek, receive and impart information and ideas of all kinds, regardless of frontiers, either orally, in writing or in print, in the form of art, or through any other media of his choice.”
And the Nebraska Attorney General protected doctors and pharmacists in Nebraska from their Boards, explicitly allowing them to prescribe HCQ and IVM. His opinion is a tour de force, which goes into detail about why the CDC, FDA and NIH guidelines are contradictory, unscientific and should not be followed. It should be cited in every case.
I also plan on reminding them that the FDA got its ass handed to them in court last week during a hearing of Paul Marik, Mary Tally Bowden and Robert Apter’s suit against the FDA. From an Epoch Timesarticle on the hearing:
“FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID,” Ashley Cheung Honold, a Department of Justice lawyer representing the FDA, said during oral arguments on Aug. 8 in the U.S. Court of Appeals for the 5th Circuit.
The statements “don’t prohibit doctors from prescribing ivermectin to treat COVID or for any other purpose” Ms. Honold said.
“FDA is clearly acknowledging that doctors have the authority to prescribe human ivermectin to treat COVID. So they are not interfering with the authority of doctors to prescribe drugs or to practice medicine,” she said.
So, if the FDA recognizes we have the authority to prescribe ivermectin, then assuredly we are allowed to have the opinion that it is a valid therapy. However, the ABIM will not allow an ABIM certified physician to publicly express this opinion or recommend this practice. Maybe the ABIM should have a little chat with the FDA?
The nonsense doesn’t end with the ABIM, as they are only one prong of this campaign. How is this for some comic relief, published last week in one of the top journals in the world where they found that almost all the Covid misinformation in the U.S on social media can be traced to 52 doctors.
I was honored to discover that yours truly made the list! In their quoted examples of misinformation in Table 4, I have taken the liberty of owning up to the posts attributed to me, all of which I stand by to this day:
I think I will finish with this excerpt from a recent Wall Street Journal op-ed touching on the Missouri vs. Biden case where the administration is being sued for its systematic censoring of U.S citizens on social media by every intelligence and health agency in our Federal government :
This is where the decision of U.S. District Judge Terry Doughty sheds light. His detailed recounting shows a Washington energetic in protecting Americans from Covid opinions, expertise and claims that conflicted with its own, at a time when it served politicians to show they were trying to save Americans from encountering a virus that couldn’t be avoided. When government has a message to deliver, especially when the political stakes are high, it won’t be content just to push its own message, it will try to silence others. Fighting back will always be necessary. The only surprise in our age is how thoroughly the “liberal” position has become the pro-censorship position (that last line is a doozy).
New documentary about journalist Seymour Hersh uncovers the pathologies of US imperialism
By Leon Hadar | The American Conservative | January 2, 2026
Laura Poitras and Mark Obenhaus’s new film Cover-Up is more than a documentary about the legendary journalist Seymour Hersh—it is an inadvertent chronicle of the pathologies of American empire. As a foreign policy analyst who has long advocated for realist restraint in U.S. international engagement, I find this film both vindicating and deeply troubling. It documents, through one journalist’s extraordinary career, the pattern of deception, overreach, and institutional rot that has characterized American power projection for over half a century.
What makes Hersh’s reporting invaluable from a realist perspective is that it consistently exposed the gap between stated intentions and actual policy outcomes. CIA domestic surveillance, the My Lai massacre, the secret bombing of Cambodia, Abu Ghraib—each revelation demonstrated what realists have long understood: that idealistic rhetoric about spreading democracy and protecting human rights often masks cruder calculations of power, and that unchecked executive authority in foreign affairs inevitably leads to abuse.
The documentary’s treatment of Hersh’s Cambodia reporting is particularly instructive. Here was a case where the American government conducted a massive bombing campaign against a neutral country, killing tens of thousands of civilians, while lying to Congress and the public. This wasn’t an aberration, but the logical consequence of what happens when a superpower faces no effective constraints on its use of force abroad. In exposing the scandal, Hersh also documented how empire actually functions when stripped of its legitimating myths. … continue
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The word “alleged” is deemed to occur before the word “fraud.” Since the rule of law still applies. To peasants, at least.
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