Table of Contents
- 1 The Vaccines:
- 1.1 A Brand New Technology:
- 1.2 The Spike Protein:
- 1.3 Increase Deaths and Injuries Reported in VAERS:
- 1.3.1 How VAERS works:
- 1.3.2 Dr. Jessica Rose and the Clustering of VAERS Reports:
- 1.3.3 Dr. Tess Lawrie and the UK’s Yellow Card Program:
- 1.3.4 Dr. Scott McLachlan and 86% Post-Vaccine Deaths in VAERS:
- 1.3.5 Myocarditis in Young Men Following 2nd mRNA Vaccine Dose:
- 1.4 The Nuremberg Code and Informed Consent:
- 1.5 The CDC’s MMWR Report “Vaccines Don’t Work”:
- 1.5.1 Difference Between Infections and Hospitalizations/Deaths:
- 1.5.2 The Kaiser Permanente Cohort Study:
- 1.5.3 Differences between Pfizer and Moderna Vaccines against Delta Variant:
- 1.5.4 mRNA vaccines more effective than no vaccines against infection:
- 1.5.5 mRNA vaccines still very effective against hospitalizations and death:
- 1.5.6 19% Death Rate for the Vaccinated:
- 1.6 COVID-19 in Pregnancy:
- 1.7 Vaccines Creating a “SuperBug”:
- 1.8 Not a Single Failure of Natural Immunity:
- 1.9 Hard to Transmit the COVID-19 Virus:
- 1.10 The Vaccinated are Killing the Unvaccinated:
- 1.11 Risks of mRNA Vaccines vs. Risks of COVID-19:
- 2 Early Treatment:
- 3 Summary (5-minute read):
- 3.1 VAERS Reporting:
- 3.2 The Vaccine’s Spike Protein:
- 3.3 The Efficacy of the Vaccines:
- 3.4 Vaccines and “Superbugs”:
- 3.5 The Vaccinated vs. the Unvaccinated:
- 3.6 Early Treatment Protocols:
- 3.7 The Swiss Cheese Analogy:
- 4 Bio of Dr. Sean Pitman
- 5 Addendum:
Last Update: 9/6/2021
This past weekend The Villiage Seventh-day Adventist Church, in Berrien Springs, Michigan hosted a “COVID Coercion and Conscience” weekend (August 20-21) “With Dr. Peter McCullough – A Nationally Recognized Leader in Early Treatment of COVID-19“.
Dr. Peter McCullough is an American cardiologist. He is former Vice Chief of Internal Medicine at Baylor University Medical Center in Dallas, Texas, and professor at Texas A&M University. He is editor-in-chief of the journals Reviews in Cardiovascular Medicine and Cardiorenal Medicine. While only being 58 years old, he has managed to publish over 650 peer-reviewed papers, which is a real accomplishment.
This past Friday evening (8/20/21), Dr. McCullough started off the weekend with a 1.5-hour talk about the worldwide COVID-19 pandemic, the vaccines against COVID-19, and early treatment protocols (Link). Already, as of 8/22/21, this video has been viewed over 60,000 times! So, the interest is very strong regarding the pandemic we’re in and how to best go about dealing with it. The problem for me is that, while Dr. McCullough did present a few helpful ideas and concepts that are well-supported by empirical evidence, he also made quite a number of key claims that seriously misrepresent the data that is currently in hand. My fear is that the misinformation that Dr. McCullough is effectively spreading will end up hurting many people. So, while I’ve previously addressed a number of McCullough’s mistaken claims along these lines (Link), I’ve decided to review the additional key claims that he presented at the Villiage Seventh-day Adventist Church this past weekend (Link).
Note: This article is fairly long and detailed. For a 5-minute Review / Summary: Link
A Brand New Technology:
Dr. McCullough started off talking about the vaccines that are currently being used against COVID-19 – both RNA- and DNA-based vaccines. He pointed out that these vaccines are a “brand new technology” and that it is impossible to know if these vaccines will be effective, much less safe, given the limited time that they were studied before being brought to the general public worldwide.
The 1976 Sine Flu Fiasco:
As an illustration of the potential for problems, he cited the situation where a vaccine was produced to fight the swine flu (in 1976), noting that just 32 deaths, and some ~500 cases of the rare syndrome Guillain-Barré, out of ~45 million people vaccinated (about 20% of the US population) caused by this vaccine, shut down this vaccine program. He went on to note that “typically over 50 deaths will halt a vaccine in the US”.
As far as the deaths associated with the vaccine at the time, as reported in various new articles, these varied in different reports from 25 to 32. The National Center for Biotechnology Information (NCBI) says that by 22 October 1976, 41 deaths amongst people who had been given the vaccine had been reported by the CDC, but there was “still no known connection to the vaccine” (Link). As is the situation today with the vaccines against COVID-19, deaths without a proven link to the vaccine became the focus of intense media coverage in 1976. Another NCBI article (Link) points to the intense media activity surrounding the death of three elderly people who received the vaccine at the same clinic. Again, however, there was no evidence the deaths were caused by the vaccine. Rather, it seems as though this vaccine program was stopped, not so much because of vaccine-related deaths, but because of the growing number of cases of Guillain-Barré syndrome (GBS) – a condition that causes paralysis.
The vaccination program was halted in December 1976, days after the Centers for Disease Control and Prevention (CDC) reported a number of cases of GBS among individuals after vaccination. At the time, a consensus was reached that the number of GBS cases was in excess of what would normally be expected, but later research has since found that the chances of developing the condition after vaccination are extremely small (approximately one additional case of GBS for every 100,000 people who got the swine flu vaccine).
[Dr. McCullough] also invokes a comparison beloved of antivaxxers, the 1976 swine flu vaccine, which was associated with a rare incidence of Guillan-Barré syndrome, which is a canard. Basically, antivaxxers claim that the program was killed after 500 cases of Guillain-Barré syndrome and 25 deaths, except that the evidence of association with the vaccine was unclear and there was no transmission of H1N1, leading the CDC to end the program early…
See the difference? In 1976, there was no transmission of H1N1 going on and a question of whether the H1N1 vaccine being used at the time had an association with Guillain-Barré syndrome. Under such circumstances, it was hard to argue for continuing the vaccination campaign. Fast forward 45 years, and we still have widespread community transmission of COVID-19, with the overall death toll approaching 600K in the US alone. It’s an entirely different situation.
Comparison with COVID-19 Vaccinations:
So, how does this compare with the modern vaccines against COVID-19? The VAERS data suggests a possible association with GBS and the Janssen (Johnson and Johnson) vaccine (the number of reported cases of GBS was higher than expected for the “background rate”) at ~7.8 cases per million doses among adults. Currently, however, there is no evidence of increased risk for GBS with the mRNA vaccines. (ACIP Presentation, July 22, 2021)
And, as far as the deaths associated with the vaccines, these are also extremely rare, despite the common misinterpretations of the VAERS database – as discussed further below:
The Origin of mRNA and DNA Vaccine Technology:
What Dr. McCullough does not clearly explain is that the mRNA technology and other technologies behind the modern vaccines against the COVID-19 virus (to include the DNA-based vaccines) aren’t exactly “new” or “experimental”. They’ve been around and have been carefully studied now for over 30 years! – based largely on the work of Katalin Karikó, Ph.D.
Moderna was founded in 2010 to produce vaccines based on the new mRNA technology, and the company had been growing as a vaccine manufacturer when the COVID-19 virus became a pandemic early in 2020. BioNTech is a German company established to work on immunotherapies in 2008 by a Turkish couple, who immigrated to Germany. Like Moderna, BioNTech recognized the value of the mRNA technology for vaccine design years ago and licensed the technology. In 2013, BioNTech hired Karikó as a vice president and began to develop mRNA technologies for use against many diseases. BioNTech’s efforts in vaccine development greatly increased in 2018, when Pfizer joined BioNTech’s effort with a research and development agreement to develop mRNA-based vaccines against influenza. It was a natural collaboration because Pfizer, a U.S. company in New York, has been a major vaccine producer for a long time. When the pandemic began, Pfizer/BioNTech immediately turned their attention to developing vaccines against COVID-19. (Link, Link)
It’s not like there’s some deep mystery here as to how they fundamentally work. We know very well how they work (Link). And, Dr. McCullough is not against vaccines in general. He has taken dozens of vaccines himself – as he freely admits. So, what’s his real problem with the vaccines against COVID-19? Well, it’s his fear of the “spike protein”. He also throws in some possibilities of some future “cancer risk” or “birth defects”, but doesn’t explain why such risks wouldn’t have been detected well before now – given the 70,000 people involved in the original double-blinded placebo-controlled trials (not to mention the animal trials, or the hundreds of millions of people who have since been vaccinated). He does say that such risks usually require “two years” before they can be effectively ruled out for a new vaccine. However, his primary concern seems to be with the spike protein produced by the vaccines.
Comparison with Patisiran mRNA to Treat ATTR:
Patisiran, sold under the brand name Onpattro, is a medication for the treatment of polyneuropathy in people with hereditary transthyretin-mediated amyloidosis (first used in 2017). Hereditary transthyretin-mediated amyloidosis is a fatal rare disease that is estimated to affect 50,000 people worldwide. The per-patient cost is between $451,000 and $677,000 per year, depending on the number of vials needed (Link, Link)
So, why do I bring this up? Because, Patisiran is based on the very same mRNA technology used in the Pfizer and Moderna vaccines. It uses lipid nanoparticles to deliver specially coded mRNA into human cells to produce the desire protein sequences to treat disease. About 1,000 people have been using Pitisiran since 2017. Now, the mRNA vaccines against COVID-19 use two injects of 30μg (Pfizer) to 100μg (Moderna) of mRNA for each injection. In comparison, Patisiran uses around 100x this dose of mRNA, which gets injected intravenously every three months . . . indefinitely since 2017. And, this was done with good safety as well as efficacy results (Link).
See also the discussion of Patisiran by Dr. Steve Lee: Link
The Spike Protein:
The main fear of Dr. McCullough, when it comes to the vaccines against the COVID-19 virus, all boils down to the “spike protein” that is produced by these vaccines. Spike proteins are found on all coronaviruses, not just the SARS-CoV-2 virus. For example, the “common cold” is caused by coronaviruses (such as HCoV-229E). And, they all have “spike proteins” on their surfaces. And, most of us do just fine when it comes to making it through a common cold. So, what’s so bad about the SARS-CoV-2 spike proteins that have been used as “targets”? – as the product of the modern vaccines against COVID-19?
Well, according to Dr. McCullough, these particular spike proteins of SARS-CoV-2 were deliberately manipulated and design, by laboratory scientists, specifically to infect and kill people. In other words, Dr. McCullough believes that these particular spike proteins were not naturally produced, but were produced by humans as a type of bioweapon. What evidence does he have for this? He doesn’t say…
What he does say is that this extremely harmful and dangerous spike protein is not only produced at the site of vaccine injection (according to the information coded by the vaccine’s DNA and/or RNA that was “made to last” longer than natural RNA or DNA sequences), but that this spike protein, once produced, goes throughout the body causing damage to every organ in the body – to include the heart, brain, adrenal glands, and ovaries in particular. He claims that the spike proteins can “circulate in the body for between 2 weeks and 9 months – and can even be passed on from one cell to “daughter cells” after cell division.
The Japanese “Biodistribution Study”:
If true, this all sounds very scary indeed! So, what evidence does Dr. McCullough offer to back up these scary claims? Well, he starts off by citing a “biodistribution study” obtained from the Japanese Pharmaceuticals and Medical Devices Agency (Link, Link in English). He said the study shows how the coronavirus spike protein circulates in the bloodstream of vaccinated individuals and accumulates in their organs. First off, however, this particular study didn’t deal with the spike proteins at all, only with the distribution of lipid nanoparticles – which Dr. McCullough alludes to via a very quick reference to “nanoparticles”, but without explaining that these nanoparticles are tiny lipid droplets used in vaccine transport – not the spike proteins produced by the vaccines at the site of injection.
“The document is a real (common technical document), though it’s not leaked – it’s part of the submission data applied by Pfizer to PMDA (Japan’s version of FDA) for its review,” Kit Longley, senior manager of science media relations, said in an email. “The document is about the pharmacokinetics overview seen from lab studies and we can confirm it’s not about spike proteins from the vaccine resulting in dangerous toxins that linger in the body.” (Link)
Beyond this, Dr. McCullough doesn’t seem to understand what the paper is actually saying about the distribution of the lipid nanoparticles from the vaccines either.
Vaccine Lipid Nanoparticles Accumulate in the Ovaries of Women:
The common claim (among anti-vaxxers and Dr. McCullough lately) that lipid nanoparticles from the mRNA vaccines accumulate specifically in the ovaries of women, producing infertility, is also based on this same Japanese Biodistribution Study. However, the way this claim is presented, and the implications suggested by Dr. McCullough, are inaccurate and very misleading.
The biodistribution study found that the injection site retained the highest concentration of lipid nanoparticles, not the ovaries.
This data was obtained by injecting rats with a mix of lipid nanoparticles, which are identical to the ones used in the COVID-19 RNA vaccines, that carry a radioactive “label” (deuterium). Researchers then then measured the level of radioactivity in tissues at different time points after injection. The level of radioactivity acts as a proxy measurement for how much lipid nanoparticle is present in a given tissue. Changes in the level over time provide scientists with an idea of how long it takes for the body to eliminate the particles.
The article’s interpretation of the biodistribution data is inaccurate. As Abraham Al-Ahmad, an associate professor in pharmacology at Texas Tech University, pointed out in a blog post, the data showed that the injection site had the greatest accumulation of lipid nanoparticles, followed by the liver. Specifically, the peak concentration at the injection site was 52.6% of the administered dose at one hour post-injection. That of the liver was 18.1% of the administered dose at eight hours post-injection (see Table 1). A microgram is one-millionth of a gram.
However, instances of this claim, as seen in the TrialSite News article, tend to omit the table containing the data for the liver and injection site, instead drawing attention only to the data for the ovaries.
The peak concentration in the ovaries, occurring at 48 hours post-injection, was just 0.095% of the administered dose (see Table 2). [or less than 1:1,000 of the total dose of lipid nanoparticle. 50% was metabolized by liver. Brain peak was 0.02% (1/5000 of the total dose)]
Apart from the inaccurate interpretation of data, another critical aspect of the biodistribution experiment that TrialSite News failed to consider is the amount of lipid nanoparticles administered in the rats and its relevance, or more precisely, its lack thereof to the amount present in RNA vaccines given to people.
The study administered 50 micrograms of lipid nanoparticles to each rat. As explained by David Gorski, a professor of surgery at Wayne State University and editor of Science Based Medicine, this would effectively translate to a much higher dose in rats than in humans [a does of ~18-35x higher than the typical adult human dose]. This is due to the large difference in body weight:
In other words, the dose administered to rats was far higher than the dose used in people. There isn’t evidence showing that COVID-19 RNA vaccines are causing fertility problems.
Also, why would lipid nanoparticles (tiny fat droplets) be harmful to the human body? The fats that we eat are absorbed and generally distributed and used throughout the body as well – without any problems. What is so concerning about the lipid droplets used in the mRNA vaccines? Where is the evidence that they would or could cause any negative effects on the ovaries? – or any other organ system within the human body?
There have been actual studies of COVID-19 vaccines and ovarian function. In one such study, for example, researchers studied women undergoing oocyte retrieval for in vitro fertilization. They found no detrimental effect on ovarian follicular function. Another study of women undergoing in vitro fertilization demonstrated that the Moderna COVID-19 vaccine has no detectable effect on the percentage of clinical pregnancies resulting from the procedure. Yet another study has shown that vaccination against COVID-19 has no effect on immunological tolerance of the fetus by the mother. Still another study failed to find any effect on embryo implantation rates between SARS-CoV-2 infection seropositive, SARS-CoV-2 vaccine seropositive, or seronegative women. (Link)
Scientists at the University of Guelph’s Ontario Veterinary College also say that McCullough’s claims are completely wrong here.
“The bottom line is the vaccine contains an altered protein that is designed to prevent full activation, and it circulates for a short period of time at levels that are far below what would be a concern,” W. Glen Pyle, a professor in the Department of Biomedical Sciences, said in an email.
J. Scott Weese, an associate professor in the Department of Pathobiology, said in an email that all evidence suggests the coronavirus vaccines are safe. Misinformation about the safety of the vaccines appears to be aimed at “creating fear and confusion during a critical time in this pandemic,” he said.
“The efficacy and safety of mRNA vaccines is astounding, to me, particularly for a virus we’ve only known for a year and a half,” Weese said. “mRNA vaccines have been used on millions of people, including extremely high rates of vaccination in high-risk populations (elderly, patients with other diseases), with incredibly low adverse event rates.” (Link)
Very Few Spike Proteins Make it to Bloodstream:
Again, the basic facts here are that the vast majority of the spike proteins produced by the vaccines against the COVID-19 virus remain local at the injection site. Very few make it to the bloodstream, and those that do circulate in the bloodstream are not toxic because of three reasons:
- There just aren’t enough of them to produce toxicity.
- The few spike proteins that do make it into the blood are almost all filtered out by the liver.
- The spike proteins produced have been modified to reduce bioactivity within the body.
Some of the vaccine dose is going to make it into the bloodstream, of course. But keep in mind, when the mRNA or adenovirus particles do hit cells outside of the liver or the site of injection, they’re still causing them to express Spike protein anchored on their surfaces, not dumping it into the circulation. Here’s the EMA briefing document for the Pfizer/BioNTech vaccine – on pages 46 and 47, you can read the results of distribution studies. These were done two ways – by using an mRNA for luciferase (and thus looking at the resulting light emission from the various rodent regions!) and by using a radioactive label (which is a more sensitive technique). The great majority of the radioactivty stays in and around the injection site. In the first hours, there’s also some circulating in the plasma. But almost all of that ended up in the liver, and no other tissue was much over 1% of the total…
In the Moderna, Pfizer/BioNTech, J&J, and Novavax vaccines, the Spike protein has some proline mutations introduced to try to hold it in its “prefusion” conformation, rather than the shape it adopts when it binds to ACE2. So that should cut down even more on the ability of the Spike protein produced by these vaccines to bind and produce the effects noted in the recent papers. (Derek Lowe, May 4, 2021)
The S1 protein started showing up as early as the first day after vaccination, peaked at around day 5, and was undetectable by day 14… The mRNA from the vaccine starts being picked up and translated into protein almost immediately, as is clear from the quick detection of S1 protein. That’s there because it’s been cleaved off the full Spike protein, but the reason that the Spike itself isn’t found (at least at the limits of detection in the assay, and it’s a really good assay) is because it’s bound to the cells where it’s produced, by the transmembrane anchor region (discussed in that earlier post I referenced above). The reason that no S1 protein is found after the second vaccination is clear – by then, a robust antibody response to it has had a chance to develop, and the protein gets rapidly cleared from the blood, just like it’s supposed to…
It seems clear from all these human trials and the clinical experience to date that the circulating levels of the S1 protein (or the Spike itself) that are sufficient to induce a protective immune response are not in themselves toxic. The animal studies demonstrate that the Spike or S1 can indeed have bad effects on living cells and tissues all by themselves, but the conditions under which this was demonstrated are not those that obtain after vaccination.
And this latest paper showing circulating S1 protein after vaccination? Coupled with the previous paper from the same group, it in fact provides strong evidence that such blood levels are not by themselves the cause of coronavirus symptoms and tissue damage. No, if you want to try for severe, permanent damage, you will need to get infected by real SARS-CoV-2 itself and take your chances. Try your luck, if you like, with the short-term symptoms and with “long Covid” symptoms as well. See if you stay out of the ICU, or if you retain your sense of smell – try them all. If you would rather not spin that wheel, and you shouldn’t, then my strong, heartfelt advice is to get vaccinated. Because then you will be protected.
In short, this claim simply isn’t based on what most medical scientists would call reasonable information.
Increased Rate of Miscarriage in Humans and Animals following Vaccination:
Still, Dr. McCullough argues that the Japanese Biodistribution Study (discussed above) is supported by evidence for increased miscarriages in humans as well as in animal studies.
That’s another very scary claim, if true. So, upon what is this claim based?
Placental Syncytin-1 Protein:
Well, a widely shared petition (December 1, 2020) from Michael Yeadon (a former scientific researcher and vice president at Pfizer Inc.), claimed the coronavirus’s spike protein contained within the Pfizer and Moderna vaccines was similar to a protein called syncytin-1, involved in forming the placenta. He speculated that this might cause antibodies against the virus to attack a developing pregnancy, too.
Some experts believe this was the origin of the whole belief that Covid vaccines might harm fertility (Link). In reality, however, syncytin-1 and the coronavirus’s spike protein are just about as similar as any two random proteins – so there really is no good reason to believe the human immune system might confuse them, to begin with. And, as far as I’m aware, no published data have shown any problems with human fertility or an increase in miscarriages following vaccination. On the contrary, studies have also been done showing the miscarriage rate among vaccinated people was in line with the rate expected in the general population – 12.5%. (Shimabukuro, June 17, 2021)
But what about the animal studies cited by Dr. McCullough? Well, they show the opposite of what McCullough claimed in his talk.
There were no effects of BNT162b2 [Pfizer] on female [rats] mating performance, fertility, or any ovarian or uterine parameters nor on embryo-fetal or postnatal survival, growth, physical development or neurofunctional development in the offspring through the end of lactation (Bowman, et. al., May 28, 2021).
Increase Deaths and Injuries Reported in VAERS:
As usual, Dr. McCullough put a great deal of emphasis on the VAERS reporting system (Vaccine Adverse Events Reporting System – maintained by the CDC and the FDA), noting that over 12,000 deaths had been reported to VAERS following vaccination against COVID-19 (as of July 30, 2021) with 40% of these deaths occurring within 3 days of vaccination – compared with a usual rate of just 155 reported deaths annually. He notes that this sudden spike in reported deaths in the VAERS system has “never been seen in medicine”. In a previous talk, he argued that this is likely an underreport of the true number of deaths following vaccination by a factor of 10 (Link). In other words, Dr. McCullough believes that the COVID-19 vaccines are likely responsible for over 120,000 deaths so far – calling it one of the worst national disasters ever. He claims that his interpretation of this data is so obvious that those doctors and scientists who have published papers saying that these features of VAERS are “not related to the vaccines” are committing “malfeasance” – or intentional conduct that is wrongful or unlawful.
Dr. McCullough is also shockingly ignorant of how VAERS works. He claims that only a health care worker can access the system and that a patient or a loved one has to contact a physician or health care worker to enter a report. That is completely wrong. Indeed, one of the complaints about VAERS is that anybody—and I do mean anybody—can enter a report. It is this openness that is simultaneously one of VAERS greatest strengths and weaknesses. It’s a weakness in that this openness allows for gaming of the system, as lawyers for parents seeking to sue vaccine manufacturers for autism as a “vaccine injury” did 15 years ago. Seriously, this is an error huge enough to make me wonder about everything else, in particular whether he got his MPH out of a cereal box. This guy has an MPH and doesn’t know (or didn’t bother to find out) how VAERS actually works and that there are other vaccine safety monitoring systems other than VAERS?
How VAERS works:
This sounds horrible! How could the government be allowing this sort of catastrophe to be happening in this country?! Well, things aren’t always as they may seem on the surface – even for a doctor like Dr. McCullough. It has to do with the nature of the VAERS reporting system. People can report anything to VAERS without any kind of demonstration of a causal link to a vaccine or anything else. The fact of the matter is that even if I were to simply wave my hand over the foreheads of a population the size of the United States that nearly 8,000 people would die that very same day (Link). So, it only stands to reason that, out of the 178 million Americans who have currently received at least one dose of a vaccine against COVID-19 (54%) that many tens of thousands of people would have died, for various reasons, within three days of being vaccinated. Here’s another commentary to illustrate this point:
There were 293 deaths reported to VAERS during the last week of April. That sounds like a large number, particularly when, averaged out, it translates to 41.9 deaths per day. But is it? How many people received COVID-19 vaccines that week? By subtracting the April 23 statistic from the April 30 statistic, I come up with 7.66 million people receiving a COVID-19 vaccine during the last week of April, or 1.1 million/day. How many deaths would we expect in a week in a population of 7.66 million in a week, based on the CDC’s pre-pandemic statistics? Using the aforementioned yearly incidence of death pre-pandemic of 868.7 per 100,000 in a year, we can say that in a population of that size there would be 66,619 deaths in a year, or 182.5 deaths per day or 1,278 deaths in a week… Think of it this way. Never before in the history of VAERS has there been a mass vaccination program like that for COVID-19. The population initially targeted vaccination was exactly the population that has the highest baseline death rate, meaning that by random chance alone we would expect to see a seemingly large number of deaths within days of vaccination.
But there’s yet another factor. Those who have received a COVID-19 vaccination know that all those who receive COVID-19 vaccines are given instructions to sign up for V-Safe, a monitoring system that works by text message. Basically, if you sign up for V-Safe, you will receive periodic text messages, starting as daily text messages that become less frequent over time. I note that, even though I completed my vaccination series in January, I still receive V-Safe texts periodically. This basically turns a passive surveillance system into a quasi-active surveillance system. And, remember, the more you look for something, the more you will find. Always.
The law of large numbers says that, whenever an intervention is administered to huge numbers of people, there will be large numbers of adverse events that happen after that intervention by random chance alone. The way scientists determine if there is a safety signal in those adverse events is by comparing them to the expected baseline rate of each adverse event. The bottom line is that, fear mongering articles by RFK Jr. and reports of a “vaccine Holocaust” to the contrary, there is no evidence of deaths above and beyond what one would expect based on known baseline rates of death in the US population. Although RFK Jr. might not be expected to know this, someone like Dr. McCullough, who has an MPH in addition to his MD, should really, really, really know better. That he promotes antivaccine disinformation based on fear mongering about reports to VAERS of deaths and adverse events tells me one of two things. Either his MPH education failed him, or he’s lying. Take your pick. .
So, for Dr. McCullough to claim that the vaccines are clearly responsible for deaths reported to VAERS following vaccination is clearly misguided. The fact is that he has no evidence whatsoever that the vaccines were responsible for these deaths. Rather, the intended purpose of VAERS is to detect patterns that occur above and beyond normal background levels for large populations – like the US population. And, so far, the vaccines against COVID-19 have proven themselves to be not only very effective against COVID-19, but also very safe. While some serious risks have been detected, these risks are very rare (Link).
But what about the graph shown by Dr. McCullough that demonstrated a dramatic increase in the number of deaths reported to VAERS since the beginning of vaccinations against COVID? After all, the usual number of deaths reported to VAERS is less than 200 per year. Why, all of a sudden, is there a spike of reported deaths to VAERS in 2021 of over 5,000 deaths? Well, this could be for a number of reasons (as Dr. Gorski pointed at above). It could be that the worldwide nature of the COVID-19 pandemic and the strong promotion of the vaccines to help fight it simply makes people much more aware and vigilant when it comes to events surrounding vaccines against COVID-19. Everyone is aware of the situation we’re in and all of the unusual restrictions. This issue has become very political instead of just a medical/scientific question – and has become very divisive as a result. It is no wonder, then, that there has been a sudden increase in reported deaths to VAERS following the COVID-19 vaccinations in particular. The very consistent V-Safe Texts also contribute to this heightened awareness for those who’ve been vaccinated. However, this doesn’t prove or even suggest, by itself without additional evidence, a correlation with the vaccines. After all, the very same type of thing has happened before. Note that during the H1N1 flu outbreak in 2009 that there was also a spike in VAERS reporting that went well above the expected background death rate.
During the period from 1 July 2010 to 6 May 2016 following the 2009 H1N1 influenza pandemic, 671 reports after influenza vaccines in pregnant women were submitted to VAERS; 544 were after IIV. This represents a decrease in the annual number of pregnancy reports following the 2009 H1N1 pandemic (Fig. 1) despite similar vaccination coverage as observed during the pandemic year, but an increase over the period 1990 – 2009 before the H1N1 pandemic. Prior to the 2009 H1N1 pandemic, pregnancy reports after IIV had been sparsely reported to VAERS. The peak in the number of pregnancy reports observed during 2009 – 2010 followed by a decrease in reporting suggests that the 2009 spike in pregnancy reports after 2009 H1N1 inactivated vaccines may have been due to stimulated reporting. During the current review, we did not observe any new AE or condition of concern. Moreover, data mining analysis did not reveal any disproportionate reporting for any pregnancy-specific MedDRA®PT. (Link)
This is what a lot of people don’t understand – including some of those with an M.D. or a Ph.D. behind their names. There is a world of difference between causation and correlation. And, sometimes, it can be very hard to tell the difference. That is why very careful scientific studies and investigations are required to determine if there is, or isn’t, a true connection between two events.
Dr. Jessica Rose and the Clustering of VAERS Reports:
But what about the paper by Dr. Rose that Dr. McCullough mentioned in his talk? – presenting the problems that the VEARS data so clearly shows for the vaccines (Rose, May 2021)?
Using vaccine data up to April 10, 2021, Dr. Rose noted that by the end of March, about 100X more COVID-19 vaccinations occurred as opposed to flu vaccinations. This was associated with 380 times more safety reports due to COVID-19 vaccinations. This means that 99% of all adverse events (AEs) currently recorded in VAERS are associated with the mass COVID-19 vaccination program. Beyond this, Dr. Rose makes the same argument as Dr. McCullough – that the clustering of deaths near the day of vaccine exposure means that the vaccines must have been responsible for these deaths.
Dr. Rose was independently following up on a challenge, published on social media, to find that the number of deaths was not evenly distributed across the days following vaccination – which would suggest a non-causal relationship. Since she found that the reported distribution is not evenly distributed, her conclusion follows that, therefore, this uneven distribution is, in fact, causal. In other words, that the vaccines are, in fact, associated with the death reported to VAERS.
So, is this true? Is the non-linearity of the reporting of deaths to VAERS following vaccination supportive of the conclusion that these deaths were caused by the vaccine? – even if these deaths are not increased beyond what would normally be expected? – as in the number of deaths expected from a saline injection or me waving my hand over the foreheads of 100 million people?
First, let’s ask the question as to the deaths reported in the 70,000 people who originally signed up for the mRNA double-blinded placebo-controlled trials (Pfizer and Moderna combined). Now, six participants died during the 44,000 person Pfizer vaccine trial, two of whom were given the vaccine while the other four people received a placebo. Of the two vaccine recipients who died, one had a cardiac arrest 62 days after a second dose of the two-dose vaccination and died three days later, while the other died from arteriosclerosis three days after a first dose of the vaccination. One of the placebo recipients died from myocardial infarction, another from hemorrhagic stroke, and two others from unknown causes. It was similar for the Modern study. Three vaccinated participants died during the study while four died in the placebo group, for a total of 7 deaths (by the cutoff date of November 11, 2020).
Now, if the mRNA vaccines were so lethal, given the conclusions of Dr. Rose and Dr. McCullough here, why wasn’t this pattern detected in the original vaccine trials for Pfizer and/or Moderna? Why, did this pattern not turn up until there was a spike in VAERS reporting? Also, why is the death rate among the vaccinated not actually spiking above expected background levels? – especially given the severity of the problem according to Dr. McCullough? I mean, with upwards of 120,000 deaths caused by vaccines in the US, you would think this would also be reflected in an increase in the death rate among those who are vaccinated that is above the expected background levels within various age categories. Where is this evidence?
I’m sorry, but it seems far more likely that the VAERS reporting spike, to include the tendency to favor reporting closer to the vaccination event, is due to the significant increase in awareness that has been associated with this pandemic – worldwide. And, this conclusion is backed up by the research study of Klein et al., (September 3, 2021) into this question. An interim analysis of 6.2 million individuals who received more than 11.8 million doses of the mRNA COVID-19 vaccines revealed no significant link between the vaccines and serious adverse events, and no clustering of adverse events close to the time of vaccination, according to researchers:
In this interim analysis of surveillance data from 6.2 million persons who received 11.8 million doses of an mRNA vaccine, event rates for 23 serious health outcomes were not significantly higher for individuals 1 to 21 days after vaccination compared with similar individuals at 22 to 42 days after vaccination.
The results, published in JAMA, showed that the risk vs. comparison intervals for incidence of ischemic stroke was 1,612 vs. 1,781 per 1 million person-years (RR = 0.97; 95% CI, 0.87-1.08); appendicitis was 1,179 vs. 1,345 per 1 million person-years (RR = 0.82; 95% CI, 0.73-0.93); and acute myocardial infarction was 935 vs. 1,030 per 1 million person-years (RR = 1.02; 95% CI, 0.89-1.18). The incidence of confirmed anaphylaxis was 4.8 (95% CI, 3.2-6.9) per 1 million Pfizer-BioNTech doses and 5.1 (95% CI, 3.3-7.6) per 1 million Moderna doses. (Link)
Dr. Tess Lawrie and the UK’s Yellow Card Program:
Dr. McCullough then goes on to cite the work of Dr. Tess Lawrie (also a big proponent of ivermectin use for COVID-19 – see below) regarding the “Yellow Card Program” in England that is very similar to the VAERS program in the US.
The Yellow Card scheme (similar to the Vaccine Adverse Events Reporting System in the U.S.) can be added to by anyone, whether a clinician or a member of the public. The scheme aims to help regulators identify potential side effects involving medicines or vaccines that had not been detected or are more common than seen in clinical trials.
Consider the following review from Ian Le Guillou (HealthFeedback.org, June 16, 2021):
However, the figures reported through the scheme are not sufficient to establish a proven side effect. The U.K.’s Medicines and Healthcare products Regulatory Agency (MHRA), which runs the Yellow Card scheme, says:
“The nature of Yellow Card reporting means that reported events are not always proven side effects. Some events may have happened anyway, regardless of vaccination. This is particularly the case when millions of people are vaccinated, and especially when most vaccines are being given to the most elderly people and people who have underlying illness.”
In other words, it may simply be a coincidence that an adverse event, such as a cancer diagnosis or a speech disorder, happened within a short period after vaccination. Detailed analysis is needed to understand whether an adverse event happens at a higher rate than would be expected in the population.
The director of The Evidence-Based Medicine Consultancy Ltd, Tess Lawrie, wrote to the head of the MHRA about the adverse events reported for the COVID-19 vaccines. In the letter, which was quoted heavily in the article on America’s Frontline Doctors, Lawrie said that she would “like to draw your attention to the high number of covid-19 vaccine-attributed deaths”. However, as previously explained, deaths or any adverse events reported through the Yellow Card scheme were not attributed to vaccination.
In the letter, Lawrie stated that she recognized the limitations of the data and understood “that information on reported Adverse Drug Reactions should not be interpreted as meaning that the medicine in question generally causes the observed effect or is unsafe to use.” However, she contradicted this by concluding:
“The MHRA now has more than enough evidence on the Yellow Card system to declare the COVID-19 vaccines unsafe for use in humans.”
As evidence for her statements, Lawrie cited the numbers of various adverse events identified through the Yellow Card scheme. However, these reports can’t be used to establish a causal relationship between the vaccine and the occurrence of an adverse event. In addition, the raw numbers lack the context necessary to establish whether the vaccines are safe for use or not. Among the factors to consider are the expected side effects from vaccination, adverse events that would have happened regardless of vaccination, and the benefits of vaccination.
Expected side effects
The figures used by Lawrie overlook the fact that most of the reported adverse events are minor and transient, consisting of expected immune system responses associated with the use of vaccines. For instance, almost half of the nervous system disorders reported were headaches, which is listed as a very common side effect of the vaccines. There are also many reports of other common side effects such as pain, nausea, fever, and fatigue. The MHRA website clarified:
“For all vaccines, detailed review of all reports has found that the overwhelming majority relate to injection site reactions (sore arm for example) and generalised symptoms such as a ‘flu-like’ illness, headache, chills, fatigue (tiredness), nausea (feeling sick), fever, dizziness, weakness, aching muscles, and rapid heartbeat. Generally, these happen shortly after the vaccination and are not associated with more serious or lasting illness. These types of reaction reflect the acute immune response triggered by the body to the vaccines, are typically seen with most types of vaccine and tend to resolve within a day or two.”
Expected adverse events in the population
About 40 million people in the U.K. have received at least one dose of a COVID-19 vaccine since December 2020. Among such a large group of people, we would naturally expect to observe many medical conditions to arise that would have happened regardless of vaccination. The numbers reported through the Yellow Card Scheme do not provide this context, which would be necessary to determine whether an adverse event is occurring at an increased rate. The MHRA said:
“The total number and the nature of Yellow Cards reported so far is not unusual for a new vaccine for which members of the public and healthcare professionals are encouraged to report any suspected adverse reaction.”
Benefits of the vaccine
Each drug or vaccine is expected to cause a certain degree of side effects. However, this is weighed against the benefits of such an intervention to establish whether the public should use it. Lawrie does not appear to consider the benefits of vaccination in reducing deaths and hospitalizations due to COVID-19. The MHRA said:
“The expected benefits of the vaccines in preventing COVID-19 and serious complications associated with COVID-19 far outweigh any currently known side effects. As with all vaccines and medicines, the safety of COVID-19 vaccines is continuously monitored and benefits and possible risks remain under review.”
The Yellow Card scheme and its equivalents in other countries have already shown their use in identifying rare adverse events that may be linked to vaccinations. Regulators investigated following reports of an extremely rare specific type of blood clot in the brain, known as cerebral venous sinus thrombosis, occurring together with low levels of platelets (thrombocytopenia). Investigations found evidence for an increased risk of these rare blood clots among younger people after receiving the AstraZeneca vaccine. This led to many countries changing the vaccination guidelines, preferring an alternative COVID-19 vaccine for younger people.
Similarly, rare occurrences of anaphylaxis (a severe allergic reaction) also led to changes in guidance and information on the choice of vaccines for susceptible individuals.
In summary, the reports identified by Lawrie do not indicate any unexpected side effects from the COVID-19 vaccines. The Yellow Card scheme does not assign a cause to medical events following vaccination. The MHRA regulatory body collects this data to prompt further investigation if they have concerns. The MHRA analyzed the data and confirmed that the benefit of the COVID-19 vaccines “far outweigh any currently known side effects”.
See also the very recent results for a very large study showing the significant reduction in risk for those who are vaccinated with Pfizer vs. those who come done with a COVID-19 infection (Barda, et. al., August 25, 2021) as well as further discussion in this article here: Link
Dr. Scott McLachlan and 86% Post-Vaccine Deaths in VAERS:
Dr. McCullough also highlights a preprint paper published by Dr. McLachlan (McLachlan et. al., June 2021) where the authors point out that, “There were only 14% of the cases [in the VAERS database] for which a vaccine reaction could be ruled out as a contributing factor in their death. Given this comment, Dr. McCullough’s headlines that “86% of deaths in VAERS have no other explanation other than being caused by the vaccines”.
But how do we actually know this? Even the paper’s abstract says that only 67% of the cases were reported by medical personnel. Even here, however, aside from the proximity of the death to the vaccination event, what other evidence is there to conclude that the vaccine was responsible for these deaths? – especially given that these deaths are not above the expected number of deaths if only saline injections were given? or a wave of the hand over the forehead? It’s not like medical providers somehow enhance the VAERS reports because of their medical knowledge. “After someone receives a COVID-19 vaccine, their healthcare provider is required by law to report all serious adverse health events, even if the provider does not think the vaccine caused that event” (Link).
Let’s take a look at the math here (illustrated above). For a population of 100,000 the “all-cause death rate” is around 869.7 deaths per year (Link). For the first 3.5 months of since the COVID-19 vaccine campaign began, around 166 million people were vaccinated. Out of this population, 421,080 would be expected to die of natural causes within 3.5 months (~106 days). That gives us an average expected “all-cause” death rate of ~4000 people per day. Yet only a few hundred of these deaths are reported to VAERS on a given day? – as per the chart above? That’s the amazing thing… that so few of the deaths that must have happened the very same day as the vaccination was given are actually reported to VAERS!
Myocarditis in Young Men Following 2nd mRNA Vaccine Dose:
Dr. McCullough noted that he sees patients who developed myocarditis (an inflammation of the heart) following vaccination for COVID-19, including one particularly serious case that doesn’t seem to be resolving and will probably end up with at least long-term damage to the heart, if not death, for a young male athlete. And, this is indeed a real, but rare, risk associated with the mRNA vaccines:
Myocarditis has been recognized as a rare complication of coronavirus disease 2019 (COVID-19) mRNA vaccinations, especially in young adult and adolescent males. According to the US Centers for Disease Control and Prevention, myocarditis/pericarditis rates are ≈12.6 cases per million doses of second-dose mRNA vaccine among individuals 12 to 39 years of age… Although the mechanisms for development of myocarditis are not clear, molecular mimicry between the spike protein of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and self-antigens, trigger of preexisting dysregulated immune pathways in certain individuals, immune response to mRNA, and activation of immunologic pathways, and dysregulated cytokine expression have been proposed. (Bozkurt, et. al., July 20, 2021).
Now, what McCullough fails to mention is that the risk of myocarditis is much higher for those who become infected by COVID-19. Even in young athletes, the rate of myocarditis following COVID-19 infection ranges from around 0.6% to 0.7% (Front. Cardiovasc. Med., 14 July 2021). That’s 6000 to 7000 young healthy athletes, per million, who come down with myocarditis following a COVID-19 infection – compared with ~12 per million following mRNA vaccination (up to 67 cases per million according to the CDC; Link).
So, either way you slice it, the odds of a young healthy person coming down with myocarditis are much greater following an infection by COVID-19 compared to the risk of myocarditis following full mRNA vaccination (by at least a ratio of 100:1). And, if one actually gets myocarditis, the risks of myocarditis are pretty much the same either way.
Myocarditis can cause sudden cardiac arrest and has been linked with 10%-20% of all sudden deaths in young athletes. COVID-19 myocarditis has been linked to several sudden cardiac deaths in patients who only had mild viral infection symptoms. (Link)
And, the same thing is true for every other risk there might be. For every risk associated with the mRNA vaccines, the very same risk is far higher for those who get infected by the COVID-19 virus.
The Nuremberg Code and Informed Consent:
But what about the Nuremberg Code? Dr. McCullough suggests that doctors and other medical providers are violating the Nuremberg Code (as well as the Declaration of Helsinki) when they give people vaccines against COVID-19 – since they are not being given adequate “informed consent” before being given the vaccine. Is this really the case?
The concept of informed consent in medical research grew largely out of unethical research projects conducted in the early 20th century, including the experiments during the Holocaust and the syphilis study done on black men without their consent in Tuskegee, Alabama, according to a paper from the Presidential Commission for the Study of Bioethical Issues, which distinguishes between the idea of informed consent for medical research and regular treatment.
The concept of informed consent in the health care setting, however, “developed from the intentional tort of battery, which protects individuals from an unwanted physical touching of the body by others having neither express nor implied consent of the person touched,” according to a paper published in the Mayo Clinic’s peer-reviewed journal. For more information on the history of all this see: Link
The CDC’s MMWR Report “Vaccines Don’t Work”:
Difference Between Infections and Hospitalizations/Deaths:
According to a report from Israel’s Health Ministry (July 20, 2021), Pfizer’s general effectiveness at preventing infections decreased as the time before exposure increased: efficacy was 79% for those who received their second dose in April, 69% for March, 44% for February, and 16% for people who were fully-vaccinated back in January – with an overall average of 42%.
This is interesting since it appears to conflict, somewhat, with the findings of another recent study (Jamie Bernal, et. al., May 24, 2021) which showed the Pfizer-BioNTech vaccine to be 88% effective against symptomatic disease from the Delta Variant 2 weeks after the second dose, compared to 93% effectiveness against the Alpha Variant. Also, just one dose was found to be 33% effective against symptomatic disease from the Delta Variant after 3 weeks and 50% effective against the Alpha Variant.
On the other hand, the Mayo Clinic data is similar to data from Israel – which had one of the fastest vaccination programs in the world. According to data published in late July, the Pfizer vaccine was just 40.5% effective at preventing symptomatic disease.
Interferon Production and the Enhanced Childhood Resistance to COVID-19:
As a relevant aside, why is it, exactly, that children are so much more resistant to the COVID-19 virus? It’s all based on the enhancement of interferon in children as compared to adults (Loske, et. al., August 18, 2021). However, adults can also increase the rate of interferon production via the use of “fever production”. For additional information on how to effectively do this see Dr. Roger Seheult’s very interesting discussion of this topic:
The Kaiser Permanente Cohort Study:
In this line, consider a 6-month follow-up of the Pfizer vaccination in a Kaiser Permanente cohort of >3.3 million people regarding the attrition of the effectiveness of the Pfizer vaccine, over a span of four months, when it came to preventing infections by the Delta Variant (Tartof et. al., August 23, 2021). Particularly note, however, that during this same period of time that the vaccine maintained strong protection against hospitalizations (93%).
For additional helpful information along these lines, please also review the Twitter Feed of Dr. Eric Topol: Link
Dr. Topol is an American cardiologist, scientist, and author. He is the founder and director of the Scripps Research Translational Institute, a professor of Molecular Medicine at The Scripps Research Institute, and a senior consultant at the Division of Cardiovascular Diseases at Scripps Clinic in La Jolla, California. He is editor-in-chief of Medscape and theheart.org.
Differences between Pfizer and Moderna Vaccines against Delta Variant:
In any case, the Delta Variant of COVID-19 is far more infectious and transmissible compared to the original or “wild type” COVID-19 virus (Link). Early in the infection, when people are most likely to be contagious, the Delta variant seems to replicate in amounts that are perhaps 1,000 times as much as those seen in people infected with other variants, defeating immune defenses in the nose and throat for many people. It is 50% more contagious than the Alpha Variant, which was, in turn, around 50% more contagious than the original COVID-19 strain, with an incubation period of four days rather than six days – meaning people are contagious earlier. Preliminary studies also suggest that it may lead to more severe disease in the unvaccinated population. Additionally, the Delta Variant is resistant to some antibody treatments previously used to help very sick patients. Perhaps this is why a recent study from the United Kingdom showed that children and adults under 50 were 2.5 times more likely to become infected with the Delta Variant. And, since the mRNA vaccines were created to target the original COVID-19 virus, it is no surprise, then, that mutational variants will come along that are more resistant to the immunity produced by the mRNA vaccines.
But what is the reason for the difference in immunity, against the Delta Variant, between the Pfizer and Moderna vaccines? Why does the Moderna vaccine appear to have superior activity against the Delta Variant as compared to the Pfizer vaccine? Well, consider that each dose of Pfizer’s contains 30 μg of vaccine while each dose of Moderna contains 100 μg of vaccine – which translates into more than 3x the number of mRNA molecules injected for Moderna as compared to Pfizer. This is the primary difference between these two vaccines. Otherwise, the mRNA sequence, itself, is identical for both vaccines.
Number of Spike Proteins via Vaccines vs. Infection:
As an interesting aside, on average, a single mRNA is used to manufacture about 900 copies of the corresponding protein within a given cell (Link). Now, one Moderna vaccine dose contains about 4 ×1013 mRNA molecules (~40 trillion) while one dose of the Pfizer vaccine contains about 1.2 ×1012 mRNA molecules (~12 trillion). If each one of these molecules produces, say, 1000 spike proteins, that can end up producing up to ~1 ×1016 spike proteins (Link).
Now, in comparison, an infected person carries 109–1011 virions during peak infection with a total of up to 3×1012 virions over the complete course of a characteristic infection (Link). Each of these viruses has around 24 spike proteins on its surface (Link), for a total of ~1×1014 spike proteins.
So, isn’t this a problem? given that the mRNA vaccines end up producing around 100x more spike proteins within the human body as compared to an actual COVID-19 infection? Well, remember that more than 99% of the spike proteins produced by the mRNA vaccines remain at the injection site. Less than 1% makes it to the bloodstream, and most of these spike proteins are filtered out by the liver (Link). In comparison, an infection by COVID-19 spreads throughout the body with active viral replication destroying tissues and targeting the cells that line blood vessels, producing blood clots everywhere. These blood clots end up damaging various organs, including the lungs, kidneys, heart, and brain.
mRNA vaccines more effective than no vaccines against infection:
So, while the effectiveness of the mRNA vaccines against being infected by COVID-19 has dropped, it hasn’t dropped to zero. In other words, getting the Pfizer vaccine, for example, is still 42% more effective at blocking an infection by the Delta Variant of COVID-19 as compared to those who haven’t been vaccinated at all (76% better for those fully vaccinate with Moderna vs. no vaccine).
mRNA vaccines still very effective against hospitalizations and death:
What is also very important to remember here is how the mRNA vaccines affect the rate of serious sickness – i.e., hospitalizations and deaths. Those who are fully vaccinated are far far less likely to be hospitalized or die due to a COVID-19 infection as compared to those who are not vaccinated.
Before the Delta Variant came long, fully vaccinated people accounted for less than 3% of coronavirus hospitalizations nationwide and less than 1% of virus deaths. By the end of July, the Delta Variant was the cause of more than 80% of new U.S. COVID-19 cases. So, how has this affected the hospitalization/death rates of the fully vaccinated compared to the unvaccinated?
The authors of the Mayo Clinic study themselves concluded that both the Pfizer and Moderna vaccines “strongly protect” against severe disease via the Delta Variant; “The difference appears to be more about whether people get infected at all in the first place.” (Link) Dr. Shira Doron of Tufts Medical Center noted that the mRNA vaccines, while showing reduced effectiveness against infection, retained effectiveness against hospitalization of “over 95%” (Link). This is in line with another pre-print paper showing that the Pfizer vaccine is 96% effective against hospitalization after 2 doses (Julia Stowe, et. al., June 2021). This is comparable with vaccine effectiveness against hospitalization from the Alpha Variant.
Dr. Mary Ramsay, Head of Immunisation at PHE, noted that, “These hugely important findings confirm that the vaccines offer significant protection against hospitalization from the Delta variant.” (Link)
Dr. Gregory Poland, an infectious diseases physician and researcher at the Mayo Clinic, points out that the vaccines against COVID-19 are “extraordinarily effective against death, hospitalization, and severe disease.”
19% Death Rate for the Vaccinated:
Again, as noted above, Dr. McCullough’s claim that the death rate for the vaccinated is around 19%, therefore they don’t prevent deaths, is nonsense. Somehow, Dr. McCullough fails to grasp the concept that in regions with very high vaccination rates that the most deaths will be in the vaccinated group – despite being highly protective. But how can that be?
Consider a situation where 100% of a group of people were vaccinated with a vaccine that gives 95% protection. Over time, 5 people die. What percentage of these people were vaccinated? 100% – right? Is the conclusion, then, that because all of the dead people were vaccinated that the vaccine didn’t work? No. It just means that the vaccine wasn’t 100% effective.
The same thing is true, in a given age category, where more than 90% of people are vaccinated (as is true in Israel for those over the age of 60), but have between 12x and 82x the risk of serious infection as compared to someone in their 30s. Even if the vaccine’s effectiveness in preventing severe sickness and death were >90%, you’d still expect that a high relative percentage of the vaccinated would die in such a situation – at least 19% if not higher (see table below).
Jeffrey Morris, Director of the Biostatistics Division at the University of Pennsylvania (August 17, 2021)
What matters for gauging vaccine effectiveness is not the proportion of hospitalized people who were vaccinated but the proportion of vaccinated people who wind up in the hospital. In fact, a high share of vaccinated people among the very sick could just be a sign that a lot of people have been vaccinated. Let’s say that vaccines are 95% effective, reducing someone’s chance of being hospitalized from 1% to 0.05%. And imagine that in a group of 1 million people, 90% were vaccinated. We’d expect 0.05% of the 900,000 vaccinated people — that is, 450 people — to go to the hospital. By comparison, we’d have 1% of the 100,000 unvaccinated people — 1,000 people — in the hospital. The vaccinated would account for about one out of every three hospitalizations (Link). So, when analyzing data like this, one must adjust for the overall vaccination rates within a particular age category and then go from there.
The Latest Data from Israel:
As far as the data coming from Israel is concerned, in particular, it seems that despite a recent increase in the number of serious cases, including among the fully vaccinated, those who received both doses of the vaccine against COVID-19 are significantly less likely to experience severe illness, according to data released by the Israeli Health Ministry.
As of August 16, the ministry recorded 159 severe COVID-19 cases per 100,000 people among the unvaccinated over the age of 60, compared to 20 per 100,000 people among the fully vaccinated. This makes the unvaccinated elderly more than eight times as likely to experience a severe case than their immunized counterparts.
For those under the age of 60, the rate of severe illness among the unvaccinated stood at 2.4 cases per 100,000 people – 2.7 times more than the 0.9 per 100,000 among those who are fully vaccinated.
According to the data, while the risk of experiencing severe symptoms increases with age for both the vaccinated and unvaccinated, it rises much more dramatically among the unvaccinated.
Speaking with Haaretz during a live Q&A last week, Prof. Ran Balicer, chairman of Israel’s expert panel on COVID-19, said “there’s no question” that people who are unvaccinated are at a higher risk of developing severe illness from COVID-19. While the effectiveness of the COVID-19 vaccine may have waned somewhat over the past several months, those who are vaccinated are protected five to 10 times as much as those who are unable or unwilling to receive the shot, said Prof. Nadav Davidovitch, director of the School of Public Health at Ben-Gurion University of the Desert, Be’er Sheva, and head of the Israeli Association of Public Health Physicians. (Sokol, August 16, 2021)
Significantly Increasing Case-Fatality Rate with Age:
Note also that the COVID-19 fatality rate increases dramatically with age – in Israel an in the US and everywhere throughout the world. Those under the age of 40 are relatively unlikely to die due to a symptomatic infection (0.1% case fatality rate). However, those in their 70s have a mortality risk that is 30x that for someone in their 30s. Of course, more young people are getting very sick and are dying with the Delta Variant since this past July. Dr. Roger Seheult just saw two people in their 30s die from COVID this past weekend (August 27-19, 2021). One of these was the son of an Adventist physician. All in his ICU this weekend were unvaccinated.
This also doesn’t take into account the much higher rate of long-term injuries for those who don’t die. Even young people have a fairly high rate of long-term injuries following a COVID-19 infection. The University of Washington researchers reported in February that about 33% of COVID-19 patients who were never sick enough to require hospitalization continue to complain months later of symptoms like fatigue, loss of smell or taste, and “brain fog.” Overall, almost 2 million COVID-19 patients (23.2%) sought treatment for COVID-related symptoms a month or more after being diagnosed. (Link)
COVID-19 in Pregnancy:
Pregnant women with Covid-19 are 15 times more likely to die, 14 times more likely to need to be intubated, and 22 times more likely to have pre-term birth than those who are uninfected, according to a study published this month in JAMA Network Open. “I have not seen risks like this,” said Linda Eckert, professor of obstetrics and gynecology at the University of Washington. (Stein, August 23, 2021)
Vaccines Creating a “SuperBug”:
If the vaccines against COVID-19 were creating “SuperBugs”, as Dr. McCullough claims, then one might think it fairly obvious that these bugs must have come from regions of the world where the vaccine concentrations are the highest. Yet, that’s not the case. The Delta Variant, for example, originated in India where only about 4% of people are fully vaccinated. The Lambda variant, or C.37, was first identified in Peru as early as August 2020 – which has a 22% full vaccination rate. So far, nothing of the kind has originated in highly vaccinated regions such as Israel, the UK, the US, Iceland, etc. So far, then, this doesn’t seem to support McCullough’s vaccine-produced SuperBug Theory much.
Vaccines are “Spreading the Virus”:
Not only does McCullough claim that vaccines are responsible for producing “SuperBugs”, but he also claims that vaccines are responsible for “spreading the virus” – claiming that those who are vaccinated have 250x the viral load, of the Delta Variant, compared to those who are not vaccinated [1:16:20 in the video].
Now, that’s a rather shocking claim. By what mechanism would those who are vaccinated be able to produce 250x the viral load as compared to those who are not vaccinated? Sure, as previously noted, early in the infection, when people are most likely to be contagious, the Delta Variant seems to replicate in amounts that are perhaps 1,000 times as much as those seen in people infected with other variants, defeating immune defenses in the nose and throat for many people. However, this increase in viral load isn’t just present in those who are vaccinated, but in the unvaccinated as well. And, this is exactly what studies have shown (Riemersma, et. al., July 31, 2021). In fact, studies have also shown that those who are unvaccinated carry a higher viral load compared to those who are vaccinated.
The SARS-CoV-2 culture of nasopharyngeal swabs was positive in 68.6% of vaccinated HCWs versus 84.9% of unvaccinated HCWs with primary infections (p = 0.005, t-test). As the probability of culture positivity depends on viral load19, this was corrected for using a probit regression model with both viral load and vaccination status as predictors. Figure 1C shows the probability of a positive culture for a given viral load in vaccinated and unvaccinated HCWs. A positive vaccination status significantly decreased the probability of culture positivity (p = 0.002, Wald test).
Does this, then, mean that vaccinated people can transmit the Delta Variant to other people? Yes, but less often and for a lesser amount of time compared to those who are unvaccinated since the vaccine still reduces the number of infections as well as the amount of time that an infected person is infectious.
This is backed up by another recent paper that showed not only do vaccines still offer fairly good protection from getting sick with Delta, but also help an infected person clear the viral load much faster.
Serial Ct values of individuals were analyzed as a surrogate marker for the viral load. The initial median initial Ct value did not differ between unvaccinated and fully vaccinated patients (unvaccinated median Ct 18.8 (14.9-22.7), vaccinated 19.2 (15.2-22.2), p=0.929). However, fully vaccinated patients had a faster rate of increase in Ct value over time compared with unvaccinated individuals, suggesting faster viral load decline:
And, additional support is provided by yet another paper published by Martinez et al., (September 2, 2021), which showed a much lower risk of viral transmission for vaccinated people as compared to unvaccinated people (Link). The data is based on pre-Delta variants, but is still interesting given the overall context of the above-described information that is based on the Delta Variant:
Five out of six fully vaccinated individuals remained viral culture-negative throughout their enrollment period, suggesting minimal shedding of infectious virus and little to no transmission risk. They also had either undetectable or sporadic viral genome loads in the nasal swabs. These data suggest that in 2 of the 4 fully vaccinated individuals for which both saliva and nasal swabs were collected, infection was initially established within the oral cavity or other saliva-exposed tissue site and was restricted from disseminating to the nasal passages. The total number of days that vaccinated individuals tested viral culture positive was significantly fewer than both newly vaccinated and unvaccinated groups, indicating that vaccination significantly reduces infectious virus shedding.
But what about the paper cited by Dr. McCullough (Niesen et al., July 5, 2021) which showed a fairly significant decrease in genetic diversity with increasing vaccine use? Doesn’t this pose a problem when it comes to producing more and more resistant strains of the virus? Well, Dr. McCullough failed to mention that the authors of this paper disagree with his interpretation of their work since they themselves viewed vaccinations against COVID-19 as a limiting factor in the evolution of SARS-CoV-2:
This study presents the first known evidence that COVID19 vaccines are fundamentally restricting the evolutionary and antigenic escape pathways accessible to SARS-CoV-2. The societal benefit of mass vaccination may consequently go far beyond the widely reported mitigation of SARS-CoV-2 infection risk and amelioration of community transmission, to include stemming of rampant viral evolution.
Now, it’s fine to disagree with the authors of a particular paper and have very good reasons for doing so, but it might still be good to at least mention that the authors don’t actually agree with or support your conclusions regarding their work.
As far as my own personal opinion is concerned, it seems reasonable to me to see the antigen variability of the spike protein as relatively limited without a significant loss of function (the Delta Variant has 7 mutations compared to the original wild-type variant while the Delta-plus Variant, or AY.1, has 8 mutations). If the vaccinations force the virus into a corner, so to speak, where there is little room within protein sequence space left to maneuver, then that would be a good thing as far as subsequent vaccines and/or natural immunity to simply eliminate these last small regions of relative safety for the virus.
Limited Mutational Landscape:
On a more hopeful note, recent research studies suggest that the mutational “landscape”, or the various possible ways that the virus spike protein might mutate in a way that allows it to “escape” the immunity generated in response to the vaccines so far produced against COVID-19, is very “limited”. Why might this be? Well, because, if the spike protein mutates too much, it will lose its ability to attach to the ACE2 receptor on human cells – and therefore suffer a “loss of function”. So, there are only so many mutational options available to the small functionally-relevant sites of the spike protein before it no longer serves a “beneficial function” from the perspective of a virus that “wants” to cause as many infections as possible. And, that’s good news when it comes to the vaccines against COVID-19 and their ability to continue to effectively teach the human immune system how to keep fighting off the COVID-19 virus.
“The modest ensemble of mutations relative to the WT [wild type of COVID-19] shown to reduce vaccine efficacy might constitute the majority of all possible escape mutations.” (Rochman, et al., August 31, 2021)
This conclusion was also predicted by Roberto Burioni and Eric J. Topol in a letter published by the journal Nature Medicine (June 21, 2021).
Despite vigorous replication of the virus in these highly vaccinated communities, the world is yet to witness the emergence of variants able to ‘break through’ the vaccine-induced immunity. We cannot, of course, exclude the possibility of their emergence even in the near future, but molecular data gathered thus far have made it clear that the ‘evolutionary space’ that SARS-CoV-2 has for evading vaccine-induced immunity is remarkably narrow relative to that available for increases in transmission rates.
Therefore, while the world needs to remain on full alert in order to promptly detect the emergence of ‘vaccine-piercing’ variants and, in that case, rapidly update the available vaccines, there is reason for very cautious optimism.
Not a Single Failure of Natural Immunity:
But what about Dr. McCullough’s claim that while high levels of break-through infections, along with hospitalizations and deaths have been seen among the vaccinated, that there hasn’t been “A single failure of natural immunity”? Not a single failure? – really? Sure, natural immunity might have offered fairly equivalent protection, compared to the fully vaccinated, before the Delta Variant came along. A study put out by the Cleveland Clinic showed that those who previously tested positive for a SARS-CoV-2 infection did not get additional benefits from the vaccine (Shrestha, et. al., June 5, 2021). Amazingly, a COVID-19 infection did not occur in anyone over the five months of the study among 2579 individuals previously infected with COVID-19, including 1359 who did not take the vaccine. That’s truly amazing! – not a single case! Wow! Of course, Dr. McCullough failed to mention the study from Qatar that showed a very similar rate of COVID-19 infection in the vaccinated as compared to those with natural immunity (Bertollini, et. al., June 9, 2021).
The relative risk for PCR positivity was 0.22 (95% CI, 0.17-0.28) for vaccinated individuals and 0.26 (95% CI, 0.21-0.34) for individuals with prior infection compared with no record of vaccination or prior infection [emphasis added] – Bertollini, et. al., June 9, 2021
Regardless, this was still very very good news at the time! It was because of this that “herd immunity” was indeed looking very promising there for a while. I personally thought that herd immunity might be reached this fall because of this particular finding. Then, the Delta Variant came along and ruined it all.
Immunity after a previous infection “is highly variable from one person to the next — it may be barely present and not last for long for some persons,” said Dr. Richard A. Martinello, a Yale Medicine infectious diseases specialist and associate professor at Yale School of Medicine.
Perhaps this is why the Cleveland Clinic currently recommends getting vaccinated, even for those who have natural immunity from a prior infection and despite their own research, published in June before the Delta variant came along (Link).
This analysis demonstrated that natural immunity affords longer lasting and stronger protection against infection, symptomatic disease and hospitalization due to the Delta variant of SARS-CoV-2, compared to the BNT162b2 two-dose vaccine-induced immunity. Notably, individuals who were previously infected with SARS-CoV-2 and given a single dose of the BNT162b2 vaccine gained additional protection against the Delta variant. (Gazit, et. al., August 25, 2021).Sivan Gazit is a physician and researcher, deputy managing director of KSM Research and Innovation Center at Maccabi Healthcare Services..
The natural immune protection that develops after a SARS-CoV-2 infection offers considerably more of a shield against the Delta variant of the pandemic coronavirus than two doses of the Pfizer-BioNTech vaccine, according to a large Israeli study that some scientists wish came with a “Don’t try this at home” label. The newly released data show people who once had a SARS-CoV-2 infection were much less likely than vaccinated people to get Delta, develop symptoms from it, or become hospitalized with serious COVID-19.The study demonstrates the power of the human immune system, but infectious disease experts emphasized that this vaccine and others for COVID-19 nonetheless remain highly protective against severe disease and death. And they caution that intentional infection among unvaccinated people would be extremely risky. “What we don’t want people to say is: ‘All right, I should go out and get infected, I should have an infection party.'” says Michel Nussenzweig, an immunologist at Rockefeller University who researches the immune response to SARS-CoV-2 and was not involved in the study. “Because somebody could die.”..
“These results suggest that boosting vaccinated individuals with currently available mRNA vaccines would produce a quantitative increase in plasma neutralizing activity but not the qualitative advantage against variants obtained by vaccinating convalescent individuals.”.
Delta Variant More or Less Deadly:
Of course, it is also interesting to note that the current CFR (case fatality rate) in the US for the last 30 days, prior to September 6, 2021 (largely due to the delta variant) is 0.6%. Does this mean that the delta variant is, therefore, less lethal? Not necessarily since the current CFR may be reduced due to the vaccination rate and the rate of natural immunity that is much higher now as compared to the situation before 2021. Still, it is interesting to note that in June (2021), just before the delta variant became prominent in the US, the CFR was much higher at 2.6%. In May it was also higher at 1.92%. And, this higher fatality rate has remained remarkably consistent since widespread vaccinations were made available in early 2021. Then, suddenly, in July, when the Delta Variant became dominant, the CFR dropped significantly. Why would this happen so suddenly unless the delta variant were, in fact, significantly less deadly? Since hospitalizations have indeed risen in recent weeks, it is entirely possible that the death rate will rise dramatically in August, but that just hasn’t happened as in the past.
What’s the most likely reason for this? Could it be that the Delta Variant is simply less deadly compared to previous variants? Perhaps. Or, perhaps it’s just because the Delta Variant is affecting a younger population in a context of higher vaccination rates and natural immunity? That’s also possible. Dr. Amesh Adalja, a senior scholar at the Johns Hopkins Center for Health Security, said: “All variants are going to have a lower case fatality rate, because a significant portion of the population, especially those at high risk for death, are fully or partially vaccinated.” (Link)
In any case, it does seem that children are getting hit pretty hard by the Delta Variant. The hospitalization and ICU admission rates are rapidly approaching the highest pre-Delta levels (Siegel et al., September 3, 2021). Emergency department visits and hospital admissions in a 2-week period in August 2021 were higher in the 0-17 age group in states with lower population vaccination coverage and lower in states with higher vaccination coverage (Link).
Hard to Transmit the COVID-19 Virus:
The basic reproduction number (R0) of SARS-CoV-2 has been estimated to be as high as 5.7, meaning that one infected person can be expected to spread the infection to 5.7 others, on average, in a population of susceptible individuals. This number is much higher than typically seen with more common respiratory tract infections, including seasonal influenza (R0 = 1.3) and respiratory syncytial virus (RSV) (R0 = 3.0). This means the virus is extremely contagious and has the potential to spread rapidly throughout communities, as has been demonstrated. (Haston and Pickering, May 21, 2021)
The Vaccinated are Killing the Unvaccinated:
Amazingly, when McCullough, who was asked to comment on the 90-95% of covid patients in the hospital being those who are unvaccinated, claimed that they likely contracted it from the vaccinated. He was blaming the vaccinated for infecting and causing the hospitalizations of the unvaccinated (August 21 Panel Discussion). Now, while it is true that the Delta Variant has a higher rate of “break-through infections”, as discussed above, and while it is also true that this can result in an infected vaccinated person transmitting the virus to someone else, it is also true that an infected vaccinated person is less infectious and for a shorter amount of time compared to someone who is not vaccinated who gets infected (Chia, et al. July 31, 2021). Delta viral loads were similar for both groups for the first week of infection, but dropped quickly after day 7 in vaccinated people.
In this line, consider another recent preprint paper available on medRxiv:
Our data support that the SARS-CoV-2 infectious virus shedding is lower in vaccinated individuals with breakthrough infections (caused by primarily the delta variant) than in unvaccinated individuals with primary infections (caused by SARS-CoV-2 D614G). Nevertheless, virus culture was positive in 68.6% of breakthrough infections and Ct-values decreased throughout the first three days of illness. Despite the reduced viral viability, the infectivity of individuals with breakthrough infections should not be neglected. (Shamier, et. al., August 21, 2021)
Also, consider the results of the “REACT-1 Study” where the researchers found that “fully vaccinated people in this testing round had between around 50% to 60% reduced risk of infection [Delta Variant], including asymptomatic infection, compared to unvaccinated people. In addition, double vaccinated people were less likely than unvaccinated people to test positive after coming into contact with someone who had COVID-19 (3.84% vs 7.23%)” (Link). “Fully vaccinated people who were infected with the virus tended to have less severe illness than unvaccinated people and seemed to have smaller amounts of virus in samples, the researchers added, meaning they may be less likely to pass it on if they are infected” (Link).
Paul Elliott, an epidemiologist at Imperial, says that these results differ from other Ct studies because this REACT-1 study sampled the population at random and included people who tested positive without showing symptoms. (Link)
Risks of mRNA Vaccines vs. Risks of COVID-19:
When it comes to analyzing the risks of vaccination vs. getting infected by COVID-19, it would be good to review a large important scientific study of Pfizer mRNA vaccination (>884,000 people and controls) vs Covid infection (>173,000 people and controls). This study provides clear evidence regarding the relative safety of the mRNA vaccines vs. the other option of getting infected by COVID-19 (Barda, et. al., August 25, 2021). With the exception of lymphadenopathy (a benign self-limited reactive condition), pretty much every other risk one can think of for the mRNA vaccines is far surpassed when it comes to getting infected by COVID-19. In fact, getting vaccinated was substantially protective against numerous key adverse events – such as “anemia, acute kidney injury, intracranial hemorrhage, and lymphopenia.”
In this study in a nationwide mass vaccination setting, the BNT162b2 [Pfizer] vaccine was not associated with an elevated risk of most of the adverse events examined. The main potential adverse events identified included an excess risk of lymphadenopathy (78.4 events per 100,000 persons), herpes zoster infection (15.8 events), appendicitis (5.0 events), Bell’s palsy(8 excess events per 100,000 persons), and myocarditis (2.7 events – 1 to 5 events per 100,000 persons). The risk of this potentially serious adverse event [myocarditis] and of many other serious adverse events was substantially increased after SARS-CoV-2 infection. SARS-CoV-2 infection was estimated to substantially increase the risk of several adverse events for which vaccination was not found to increase the risk, including an estimated excess risk of arrhythmia (166.1 events per 100,000 persons), acute kidney injury (125.4 events), pulmonary embolism (61.7 events), deep-vein thrombosis (43.0 events), myocardial infarction (25.1 events), pericarditis (10.9 events), and intracranial hemorrhage (7.6 events).
We estimated that the BNT162b2 vaccine resulted in an increased incidence of a few adverse events over a 42-day follow-up period. Although most of these events were mild, some of them, such as myocarditis, could be potentially serious. However, our results indicate that SARS-CoV-2 infection is itself a very strong risk factor for myocarditis, and it also substantially increases the risk of multiple other serious adverse events.
Most Relied upon Slide in the World:
Do steroids, aspirin, and blood-thinners help those with COVID-19 infections survive? Sure they do.
What about monoclonal antibodies like Bamlanivimab, Casirivimab, or Imdevimab? Absolutely beneficial! In fact, Sotrovimab, the newest antibody therapy has even more remarkable breadth and efficacy. It was developed by GlaxoSmithKline and Vir Biotechnology after a large collaborative study by scientists from across the nation discovered a natural antibody – in the blood of a SARS survivor, back in 2003. Experiments have shown that this antibody, called S309, neutralizes all known SARS-CoV-2 strains – including newly emerged mutants that can now “escape” from previous antibody therapies – as well as the closely related original SARS-CoV virus.
What about maintaining a good vitamin D level before infection? or perhaps trying to improve one’s vitamin D level early on in infection? Sure, that has some reasonable data support as well (Link). What about vitamin C and zinc along with some Quercitin? I’m more neutral here, but it couldn’t hurt.
For additional recommendations from Harvard Heath (September 7, 2021): Link
Where I have problems with this “Multidrug Therapy Protocol” is with Dr. McCullough’s recommendation for drugs like hydroxychloroquine and ivermectin.
Sure, like pretty much everyone else, I was intrigued by the possibilities of hydroxychloroquine when it was first suggested as a possible treatment option for those suffering with COVID-19 infections. After all, it is a “zinc ionophore” (it helps zinc enter the cells of the human body to produce the anti-viral effects associated with zinc). Therefore, before the vaccines came along, many thought that it might at least be worth a try and were quite hopeful that it would work (Link). Unfortunately, however, this hypothesis hasn’t been very well supported by real-world scientific studies into this question. As it turns out, “Zinc supplements did not enhance the clinical efficacy of HCQ.” (Abd-Elsalam, et. al., November 2020).
But what about ivermectin? the anti-parasite drug usually used to deworm farm animals? Well, those like Dr. McCullough and Dr. Kory (who strongly supported the use of ivermectin before the US Senate). And, as with hydroxychloroquine, ivermectin seemed to show some promising results during some in vitro studies (performed or taking place in a test tube, culture dish, or elsewhere outside a living organism). However, when it came to real life with real people, actual scientific studies weren’t so promising. I wish Dr. McCullough and Dr. Kory were right about ivermectin. However, unfortunately, it doesn’t seem as though they are. That appears to be the unfortunate truth of the situation. (Link, Link)
More Background History on Ivermectin vs. COVID-19:
Now, a bit more history is interesting regarding ivermectin, in particular. I’ve had many people send me the very same meta-analysis published paper by Dr. Pierre Kory (Link) – along with the argument that ivermectin clearly works “if given early enough” following infection. The problem with these “meta-analysis” studies is that putting together an analysis on a bunch of small studies that individually have limited predictive power doesn’t necessarily make the overall meta-analysis any better than the largest and most statistically significant single underlying study. As Gorski and others point out, meta-analyses are only as good as their raw material – a phenomenon Gorski labels “garbage in, garbage out.” That’s the reason why larger double-blinded placebo-controlled trials are seen as more reliable, generally speaking, compared to meta-analysis papers. The problem here is that the preliminary results from such a trial, known as the “Together Trial” (consisting of nearly 2300 participants in a Phase 3 randomized, double-blind, placebo-controlled trial), showed no significant effect on reducing emergency room visits or hospitalizations – despite “early treatment”.
Another smaller double-blinded randomized placebo-controlled trial, involving 476 patients, also failed to show any advantage for ivermectin use (Lopez-Medina, March 4, 2021).
Now, some might suggest that the findings of these trials might be due to some sort of bias. Perhaps, but I don’t see how this is likely. This is especially true given that the particular meta-analysis paper published by Dr. Kory was published on April 22, 2021. Why might this be a problem? Because, it was published before the paper published by Dr. Ahmed Elgazzar (from Benha University in Egypt) was withdrawn because it was shown to be fraudulent (originally published on the Research Square website in November of 2020) (Link). Now, Dr. Kory’s meta-analysis paper depends heavily upon the Elgazzar paper – which is now known to be completely worthless. And, if one removes the Egypt data and re-runs the meta-analysis, “the benefit…largely loses its statistical significance.” (Link)
Now, I really wish there were clear evidence that ivermectin and/or hydroxychloroquine worked, but so far, I just don’t see the claims in this regard as being supported by the weight of evidence that is currently in hand.
Do I think Dr. Kory was lying? No. I think he really believed in and probably still believes in ivermectin as a useful treatment for COVID-19. I just think that various treatment protocols, that I think have shown some good success as described above, which are attributed to ivermectin and/or hydroxychloroquine as part of these protocols, are far more likely to be the result of some of the other drugs that are being used at the very same time – such as steroids, monoclonal antibodies, etc…
McCullough before the Senate Homeland Security Committee:
On November 19, 2020, Dr. McCullough testified, along with a number of other medical professionals, before a Senate Homeland Security Committee hearing – while holding up his “most relied upon slide in the world” (Link). He argued that the use of hydroxychloroquine earlier in the pandemic to treat outpatients with early symptoms helped to mitigate the severity of the outbreak.
“Hydroxychloroquine was widely used early on, that’s what kept the March-April-May curve down, OK?”
Dr. Harvey Risch, another of the expert witnesses from Yale University, said in his testimony that he found hydroxychloroquine in early use among high-risk outpatients to be “exceedingly safe”. He went on to testify that “studies of hydroxychloroquine early use in high-risk outpatients, every one of them, and there are now seven studies, have shown significant benefit.” (Link)
Of course, these studies were observational in nature. Dr. Ashish Jha, one of the others doctors who gave testimony, argued meant this meant that they were not of high quality – and thus the results should be treated with caution. He also pointed out that, “Hydroxychloroquine has a very narrow therapeutic range. Only a small range of doses can be tolerated without leading to toxicity. While hydroxychloroquine toxicity is not very common, its use for COVID-19 requires a higher dosage than normally employed, and therefore, raises concern of greater side-effects and toxicity.”
Overall, Dr. Jha was not pleased at all that the Senate was even having such a hearing:
The Senate Homeland Security and Governmental Affairs Committee held a hearing about early treatment for Covid-19. Yet instead of a robust discussion about promising emerging therapies or what Congress might do to accelerate such treatments, the conversation was all about the malaria drug hydroxychloroquine. That’s right. Almost nine months into the pandemic, during a surge, with 1,500 daily deaths, senators saw fit to rehash a medical dead end. Trial after trial has found no evidence that hydroxychloroquine improves outcomes for Covid-19 patients; some studies have found that it causes more harm than good…
In the hearing, I was called “reckless” because I pointed to facts that could prevent people from getting this treatment. The evidence itself, they seemed to be arguing, was the misinformation…
Senator Johnson and his witnesses questioned the integrity of the medical community, suggesting scientists were part of some “deep state” conspiracy to deny Americans access to lifesaving therapies…
By elevating witnesses who sound smart but endorse unfounded therapies, we risk jeopardizing a century’s work of medical progress. Do we really want to go back to valuing anecdote over data, and no longer use the best evidence to decide which treatments work?
And, it’s no different today. Dr. McCullough continues to promote his ideas, not via the support of careful scientific research, but via personal experience or gut feelings along with anecdotal stories which he fleshes out with appeals to weak observational studies and meta-analyses of these studies that simply haven’t been supported by the subsequent double-blinded placebo-controlled trials (on hydroxychloroquine or ivermectin).
Now, I’m all for the early treatment of those infected by COVID-19, but not with treatments where the weight of current scientific evidence simply isn’t there.
And… The Ugly:
Single Drugs Don’t Work:
So, how does Dr. McCullough respond to all the evidence that drugs like ivermectin and hydroxychloroquine don’t seem to work in real life? Well, he excuses all of these very good scientific studies by saying that you have to use “multiple drugs” as in HIV – that single drugs used by themselves “don’t work”. Of course, what Dr. McCullough neglects to mention is that in general multidrug cocktails against infections like HIV each contain drugs where each individual drug, within the cocktail of drugs being used, has at least some known benefit against the infection in question. You can’t just throw together drugs that don’t work at all by themselves and expect that they will suddenly work if used in combination – Dr. Vincent Iannelli explains (Link).
Of course, what Dr. McCullough claims to have done is to “leverage” small clinical trials and observational studies; too bad he didn’t do the RCTs of his cocktail, which, given the rapidly fatal course of severe COVID-19, would, contrary to his claim, not take “years” to get results from.
Finally, like all Brave Mavericks, Dr. McCullough claims that the reason his protocol isn’t widely accepted and publicized isn’t because it doesn’t work, but rather because the press and government regulatory agencies are either ignoring or “suppressing” news of it, even as he cited a “home treatment guide” published by—you guessed it!—AAPS. Basically, his protocol includes one FDA-accepted drug, Regeneron’s monoclonal antibody cocktail that was issued an EUA, followed by vitamins (of course!), steroids (another drug that works) and—also of course!—hydroxychloroquine, ivermectin, zinc, and azithromycin, none of which have been shown to work. Come to think of it, he’s very much like Stanislaw Burzynski, mixing the unproven with the weakly proven and claiming without evidence to have “saved thousands of lives” and claims he could have saved 50-85% of the lives lost to COVID-19. Again, there’s no solid evidence to support any of these claims. I will give him one point. He’s not entirely wrong that the US has decided to emphasize vaccination as the answer to the pandemic, but he also dismisses masking and social distancing as having been overemphasized.
Summary (5-minute read):
So, what are the most important takeaway points here? Well, for me, here’s what strikes me as the most important things to remember when it comes to the main points presented by Dr. McCullough vs. what seems to be the reality of the real-world evidence that is currently in hand:
Dr. McCullough claims that the spike in reported cases to the VAERS database of reportable adverse reactions following vaccination (maintained by the CDC and the FDA) is strong evidence that the vaccines against COVID-19 have killed over 100,000 people and have seriously injured many many more.
However, upon closer inspection, this data is best explained by enhanced reporting due to the very well-known and well-publicized, and even the politicized, nature of the pandemic that we’re in – throughout the entire world. This same kind of spike in VAERS reporting has occurred in the past during other well-publicized pandemics, so is only to be expected. Over time, as people have become more and more used to the vaccines, however, the reporting to VAERS has steadily decreased.
The Vaccine’s Spike Protein:
Dr. McCullough claims that the “spike protein” produced by the vaccines against COVID-19 are inherently very dangerous since they were originally designed, intentionally, by scientists, as bioweapons. The vaccines cause the body to produce these very same modified spike proteins, which then spread from the site if injection throughout the entire body, wreaking havoc all over the place and resulting in organ damage, infertility, and a high death rate.
This does sound worrisome, except it doesn’t actually happen in reality. In reality, the spike proteins produced according to the coding of the DNA and mRNA vaccine sequences stay local at the site of injection. Only a tiny fraction of the spike proteins ever make it to the bloodstream and most of these are filtered out and destroyed by the liver. They do not “build up” in the adrenal glands, ovaries, lungs, heart, and brains of vaccinated people and can only be detected with the use of highly sensitive equipment. The authors of the papers cited by Dr. McCullough also disagree with his interpretation of their papers. Also, the spike proteins produced by the vaccines are modified so that they simply don’t function the way that the viral spike proteins function. They can’t fold or morph in their shape like the viral spike proteins.
Now, this isn’t to say that the vaccines against COVID-19 are without any risk whatsoever. As with any vaccine or medical treatment in general, there are always risks. However, for every serious risk that is associated with the vaccines, the very same risk is much much higher when it comes to getting infected by the COVID-19 virus. In fact, getting vaccinated offers substantial protection against numerous key adverse events that are strongly associated with a COVID-19 infection – such as anemia, acute kidney injury, intracranial hemorrhage, lymphopenia, serious blood clots throughout the body, heart damage, brain damage, and especially the risk of death.
The Efficacy of the Vaccines:
Dr. McCullough claims that even if the vaccines were safe, that they just don’t work very well – especially against the Delta Variant. He shows data from Israel, the UK, and the US demonstrating a significant decrease in the effectiveness of the vaccines, over time, when it comes to blocking infection – particularly since the Delta Variant became dominant (June-July of 2021).
Sure, the evidence does show a clear decrease in the effectiveness of the vaccines over time – particularly in response to the Delta Variant of COVID-19. However, what Dr. McCullough fails to mention is that the vaccines have maintained a remarkably high and steady rate of effectiveness against hospitalizations and deaths (greater than 90%). You see, there’s a big difference between completely blocking the COVID-19 virus from infecting the nose and throat of a person (the “nasopharynx”) vs. blocking the virus from invading the bloodstream of a person and spreading throughout the organs of the body. And, since the vaccines are best able to establish a blood-based immunity, it only stands to reason that they would be less effective at blocking a mucosally-based nasopharyngeal infection since this location is not monitored as well by type of immunity that was enhanced or educated to attack the COVID-19 virus via vaccination.
Vaccines and “Superbugs”:
Dr. McCullough applies a very real fear that is known to happen when antibiotics are overused to argue that the very same thing will happen if vaccines are overused – that they will end up creating “superbugs” that become more and more resistant to vaccines. Instead, it would be much better to not use vaccines and simply find better ways to treat the infections, early during the course of infection, with other medications.
Vaccines have long been used to fight various bacterial and viral infections – with great success. Some of the most significant scourges of the past have been completely eradicated with the use of worldwide vaccination programs. The idea, then, that vaccines tend to produce “superbugs” simply hasn’t happened in the past. Why not? Well, because the human immune system is not like antibiotics that tend to target extremely specific regions (known as antigens) on bacteria and viruses. The human immune system is different in that, once it recognizes a “target” on a foreign invader it produces a spectrum of antibodies and T-cell and B-cell receptors against that target as well as to a host of potential variations of this target. This means that if the target mutates or changes over time, the human immune system is already ready for it and will still be able to recognize it despite its mutational changes – most of the time. It’s a very ingenious system, designed by God, to protect us from such infections as well as potential mutational changes over time. It’s not like God was unaware of the potential for antigen mutations when He designed the human immune system.
On top of this, consider that the variants of COVID-19 that have ended up being more infectious and more problematic compared to the original or “wild-type” COVID-19 virus have not come from highly vaccinated regions of the world, but from those regions of the world where vaccination rates are very low. This is only to be expected because mutational changes are greatest where the virus is allowed to infect and multiply the most. So, if you really want to reduce the odds of mutational variations, get vaccinated.
What is also interesting here is that Dr. McCullough is just inconsistent with his idea that the vaccines will somehow produce “superbugs” while his proposed “early treatments” with various medications will not do the same thing. If anything, his own treatment protocol would be more susceptible to this problem since it does not have the advantage of self-modification as the virus mutates.
The Vaccinated vs. the Unvaccinated:
Amazingly, when McCullough, who was asked to comment on the 90-95% of covid patients in the hospital being those who are unvaccinated, claimed that they likely contracted it from the vaccinated. He was blaming the vaccinated for infecting and causing the hospitalizations of the unvaccinated.
Now, while it is true that the Delta Variant has a higher rate of “break-through infections”, as discussed above, and while it is also true that this can result in an infected vaccinated person transmitting the virus to someone else, it is also true that an infected vaccinated person is less infectious and for a shorter amount of time compared to someone who is not vaccinated who gets infected (and who doesn’t already have natural immunity from a previous infection). So, if you want to reduce your risk of infecting someone else who might be even more at risk of a bad outcome, and you don’t already have natural immunity from a previous infection, well, get vaccinated.
Of course, recent evidence also suggests that those who have gained “natural immunity” from a previous infection are even more resistant to the Delta Variant than those who have been vaccinated – and are therefore probably even less likely to transmit the virus to others (Link). And, that is very good news! However, gaining such natural immunity is far more risky compared to getting vaccinated.
The Most Appropriate Christian Response: Link
Early Treatment Protocols:
Dr. McCullough claims that early treatment of a COVID-19 infection is vital and that his early treatment protocol would be able to essentially prevent all hospitalizations (and I suppose all deaths as well), without the need for the “dangerous” vaccinations. Here’s the diagram of Dr. McCullough’s protocol: Link
Do steroids, aspirin, and blood-thinners help those with COVID-19 infections survive? Sure they do. What about monoclonal antibodies like Bamlanivimab, Casirivimab, or Imdevimab? Absolutely beneficial! What about maintaining a good vitamin D level before infection? or perhaps trying to improve one’s vitamin D level early on in infection? Sure, that has some reasonable data support as well (Link). What about vitamin C and zinc along with some Quercitin? I’m more neutral here, but it couldn’t hurt.
Where I have problems with this “Multidrug Therapy Protocol” is with Dr. McCullough’s recommendation for drugs like hydroxychloroquine and ivermectin. While there was a lot of initial hope that these drugs might work against COVID-19 infections, unfortunately, numerous subsequent scientific studies into this question haven’t shown any useful advantages for these drugs.
When asked about this strong scientific evidence that appears to effectively counter this particular aspect of his early treatment protocol, Dr. McCullough presented the amazing argument that while these drugs may not work when given alone, that they do work in combination with this overall treatment protocol. Of course, he offers no scientific evidence for this or even a suggested mechanism as to how this might be the case. He simply says that it works the way multi-drug programs work against other viral-based diseases – such as the multi-drug protocols that are used to treat HIV infections. What Dr. McCullough fails to explain here is that each individual drug in the HIV protocols has a known beneficial effect, all by itself. This is simply not true of his own early treatment protocol for COVID-19 infections.
So, at this point, it seems clear to me that Dr. McCullough is just being disingenuous in order to save face. After all, he testified early on before the US Senate promoting his early treatment protocol as a means to save the world from the pandemic we’re in – all with minimal cost and without having to worry about masks, social distancing, or vaccines. I’m sure that, after this, he feels that his personal reputation is on the line and it’s just too hard for someone with his inflated ego to admit to an error like this.
Now, it’s not that I’m against early treatment protocols. That’s not it at all. I’m very much a fan of early treatment protocols – as long as they actually work. And, even some of the parts of the protocol used by Dr. McCullough do actually work, as noted above. Other “natural” protocols also have some useful advantages (Link, Link).
The Swiss Cheese Analogy:
To really sum everything up, I’m a fan of the “Swiss Cheese Analogy”. Everyone knows about the holes in a sheet of Swiss cheese. Now, imagine that these layers are bulletproof so that the only way a bullet can get through a layer is if it happens to go through a hole. If all one has available to protect one’s self from getting hit by bullets that are flying all around are sheets of these bulletproof layers of Swiss cheese, what this the best way to protect one’s self from all of the flying bullets? Well, it’s to put as many layers of Swiss cheese around one’s self as is possible.
Bio of Dr. Sean Pitman
Dr. Sean Pitman is a pathologist, with subspecialties in anatomic, clinical, and hematopathology, currently working in N. California.
Vaccines vs. Faith:
Others sin on the right hand. They are much too rash and reckless, tempting God and disregarding everything which might counteract death and the plague. They disdain the use of medicines; they do not avoid places and persons infected by the plague, but lightheartedly make sport of it and wish to prove how independent they are. They say that it is God’s punishment; if he wants to protect them he can do so without medicines or our carefulness. This is not trusting God but tempting him..God has created medicines and provided us with intelligence to guard and take good care of the body so that we can live in good health. If one makes no use of intelligence or medicine when he could do so without detriment to his neighbor, such a person injures his body and must beware lest he become a suicide in God’s eyes. . . ..Use medicine; take potions which can help you; fumigate house, yard, and street; shun persons and places wherever your neighbor does not need your presence or has recovered, and act like a man who wants to help put out the burning city. What else is the epidemic but a fire, which instead of consuming wood and straw devours life and body?.You ought to think this way: “Very well, by God’s decree the enemy has sent us poison and deadly offal. Therefore I shall ask God mercifully to protect us. Then I shall fumigate, help purify the air, administer medicine, and take it. I shall avoid places and persons where my presence is not needed in order not to become contaminated and thus perchance infect and pollute others, and so cause their death as a result of my negligence. If God should wish to take me, he will surely find me and I have done what he has expected of me and so I am not responsible for either my own death or the death of others. If my neighbor needs me, however, I shall not avoid place or person but will go freely, as stated above.”.Martin Luther: From a 1527 letter to a friend when a deadly plague hit Martin Luther’s town of Wittenberg (Volume 43, Pg. 132: Whether One Should Flee From A Deadly Plague – To Rev. Dr. John Hess).
The Most Appropriate Christian Response:
For many, this is a key point of misunderstanding. For example, the well-known Adventist lay evangelist, Scott Ritsema, recently wrote a response to an article published by the Lake Union Herald by Nicholas Miller (Nick is the Lake Union Public Affairs and Religious Liberty director and a professor at the Adventist Theological Seminary at Andrews University). In his response, Scott based pretty much everything on a single concept – the idea that the vaccines against COVID-19, particularly the Delta Variant, do not help to reduce one’s ability to transmit the virus to someone else.
“So, the pivotal question (the only question, really) is, does the vaccine prevent the vaccinated from transmitting the virus?” – Scott Ritsema
Scott’s own answer to this question is that vaccines simply don’t help when it comes to virus transmission.
Now, if Scott is mistaken on this point, and he is actually mistaken here, it would seem that his entire argument crumbles while Nick’s basic position remains credible – i.e., that it would be good for a Christian to get vaccinated since it does reduce the chances of one transmitting the virus to someone else – that it is the loving thing to do for one’s neighbors.
My own position here is that I would much rather convince rather than produce mandates to force vaccinations. In fact, for the most part, I think that such mandates would be counterproductive anyway – with the exception of those working in the medical field taking care of those who are sick or in nursing homes or who are otherwise immunocompromised. But what about limiting unvaccinated people from exposing themselves to many other people in general? – as in large public venues or crowded restaurants? Well, perhaps there is some similarity here to national laws against smoking in public places (as Scott points out himself). Historically, even conservative Adventists like Scott haven’t come out in opposition to such laws against smoking in public places since smoking is generally understood to be unhealthy, not just for the smoker, but for those around the smoker who might be forced to breathe in the “second-hand smoke”. Arguably, while not entirely the same, a somewhat similar situation also exists during a pandemic where an unseen virus can be unknowingly transmitted from a person to other people around him/her through the air. Now, if vaccines are known to reduce the odds of transmitting the virus to someone else, as the current empirical evidence has clearly shown, then these two situations would indeed seem to be similar – not only from a legal perspective, but from a moral perspective as well.
Now, this doesn’t mean that I’m in favor of mandates in general. I’m not. Why not if there is at least some similarity to smoking in public places? Well, I see a key difference that I think is important to consider here. I think that vaccinations are more effective at preventing personal hospitalizations and deaths compared to their effectiveness at reducing viral transmission to others. For me, this means that I favor letting people be free to make up their own minds regarding their own personal risks here – even in public settings. If one believes that the vaccines give him/her significant enough protection against the latest COVID-19 variant, which I do personally believe for myself, then why worry too much about if someone else has or has not been vaccinated? Sure, an important part of the reason why I personally chose to get vaccinated was that I wanted to reduce my chances of spreading the virus to my neighbors as much as possible – to those who might be even more at risk. However, am I willing to enforce this view of mine on others who are opposed to the vaccines? Since vaccines are generally available now for those who want them, I am now, for the most part, not willing to use mandates (with the exception of medical providers as noted above).
Health insurance companies, on the other hand, are likely to raise their rates for those who are unvaccinated since the average cost of a hospital stay for someone sick with COVID-19 is quite high – an average of ~$38,000 (privately insured patient) to ~$73,000 (patient without insurance) (Link) to over $100,000 for an ICU stay, with insurance (Link). The Affordable Care Act allows insurers to charge smokers up to 50% more than what nonsmokers pay for some types of health plans. In 49 states, people who are caught driving without auto insurance face fines, confiscation of their car, loss of their license and even jail. And reckless drivers pay more for insurance (Link). In the same way, insuring the unvaccinated is clearly a greater risk.
For Scott Ritsema’s response (and my reply) see: Link
See also the interesting commentary on this from Martin Luther in his discussion of Faith vs. the Black Death: Link
Reply from Scott Ritsema (8/27/2021):
Sean, I’ve re-read your comments this evening, and I have to make a few corrections to your statement quoted above.
First, a minor correction: it’s the head of the CDC’s argument, not mine. More importantly, though, you’ve used a word here – “reduce” – that neither I nor Walenski used, and it changes her statement completely. (I’ll assume this was sloppy of you not sneaky of you.) To be clear for our readers, here’s the argument, her words, not mine: “our vaccines… can’t… prevent transmission.” I think you agree with her on this.
As I write this I wonder what we’re debating, exactly. We are both against mandates, and I think that both of us agree with Walenski that the vaccines are failing to prevent transmission (particularly asymptomatic transmission, which was my addition to the discussion). So that’s all I’ve said. If you’re arguing beyond that, you’re arguing with somebody else, not with me. A smoke-free airplane truly prevents second hand smoke. So, mandatory vaccination and no-smoking are not at all similar; the debate over mandates ends before it begins.
You do have me curious, though. If you’re going to conflate ‘reduce’ and ‘prevent’ I would expect to see evidence that the vaccines are achieving a near-100% reduction in asymptomatic spread among the vaccinated. The link you shared didn’t provide anything on that topic. And Fauci is suggesting otherwise.
“I also think it very unwise to go around promoting the conspiratorial claims of Dr. McCullough – many of which have been shown, by careful scientific investigation, to be either significantly misleading or false. I think this will also end up causing a great deal of harm. Obviously, you believe him rather than someone like me, but time will certainly tell on this one.” – Sean Pitman
Regarding McCullough, as I said in the article, I would’ve loved to have seen the church remain neutral on vaccines. I wouldn’t have gotten involved. When I heard people getting called selfish for declining the vaccine and 100% push for the vaccine on the part of the church, I wanted the other side to be heard also. I think it’s very unwise to try to shut people down and not let them be heard and prevent people from evaluating the claims and evidence on both sides, and deciding for themselves.
So, if it’s not 100% or “near-100%”, then it’s not helpful? You talk about a “smoke-free airplane” – as in a 100% smoke-free airplane. And, that would be ideal – no question about it. However, what if one could reduce the smoke in the airplane by, say, 50%? Though not “ideal” or “perfect”, wouldn’t that be better than nothing? Clearly, it would be better than nothing – right?
So, for you to argue in absolute terms simply isn’t helpful for your cause. It makes your argument look weak and easily defeatable as long as someone can show at least some benefit to the vaccine when it comes to “reducing” the spread of the virus. And, while certainly well short of being 100% effective, particularly when it comes to the transmission of the Delta Variant, the evidence is quite clear that the vaccines do, in fact, “reduce” viral transmission.
As noted in the article I referenced for you, “While it is also true that this can result in an infected vaccinated person transmitting the virus to someone else, it is also true that an infected vaccinated person is less infectious and for a shorter amount of time compared to someone who is not vaccinated who gets infected.” (Link). Also, please consider the results of the “REACT-1 Study” where the researchers found that “fully vaccinated people in this testing round had between around 50% to 60% reduced risk of infection [Delta Variant], including asymptomatic infection, compared to unvaccinated people. In addition, double vaccinated people were less likely than unvaccinated people to test positive after coming into contact with someone who had COVID-19 (3.84% vs 7.23%).” “Fully vaccinated people who were infected with the virus tended to have less severe illness than unvaccinated people and seemed to have smaller amounts of virus in samples, the researchers added, meaning they may be less likely to pass it on if they are infected.” (Link)
Did you notice the use of the phrase “reduced risk” here? Sure, it’s not 100%, but it’s still significant, when it comes to reducing the odds of spreading the virus to someone else. One becomes less likely to be a link in the chain of transmission if one is vaccinated vs. being unvaccinated (and with no natural immunity from a previous COVID-19 infection).
Given such a situation, it would seem that a good bit of the wind in the sails of your argument disappears. If you build everything upon the concept of 100% equivalence between the vaccinated and the unvaccinated, when it comes to being able to transmit the COVID-19 virus to someone else, then, if this 100% equivalency fails, to even a moderate degree, what happens to your argument? What happens to the conclusion that, perhaps, getting vaccinated would be a loving thing to do for one’s neighbor after all?
As far as Dr. McCullough is concerned, there’s a fundamental difference between “letting people be heard” and actively promoting a particular position. You just don’t come across as a neutral party here who is simply trying to even-handedly present both sides. Rather, you seem to be going well beyond simply letting Dr. McCullough be heard. And, I’m not alone here. I think that most people would see what you’re doing as an active promotion, an endorsement, of Dr. McCullough’s claims – which is a real problem that will result in many more serious injuries and deaths.
Now, I know you don’t see it that way, but if Dr. McCullough is seriously wrong in what he’s saying, and if people take his advice to heart anyway, and end up dead or seriously injured, well, part of that could have been avoided if you hadn’t promoted and apparently endorsed him. I mean, what we do here can have very serious consequences for people.