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Critical Thinking in The Age of Censorship Pt. 2
Responding to the Fact-Checkers
In the first part of this series, I discussed many of the common errors in critical thinking I observe in our society that our academic community has failed to correct and instead has reinforced. These issues are particularly problematic within the medical field, and I would highly recommend reading the first part of this series so you can appreciate the context here.
Pseudoscience is a very loaded term that is often used to disparage any type of alternative viewpoint. Because of the inherent uncertainty in what constitutes an objective basis for the definition (as it typically ends up simply representing whatever challenges the orthodoxy), a variety of definitions have been proposed. At this point, the most universally agreed upon one is that any belief which cannot be scientifically disproven (“unfalsifiable”) constitutes pseudoscience, and this was another area I used the questioning of COVID-19’s existence to highlight.
A great challenge with Western Medicine (especially with vaccines), is that it behaves as an unfalsifiable ideology that no amount of failures can disprove. For example, by all objective metrics, the COVID-19 vaccines have failed and are either useless or have made COVID-19 worse, yet despite this, the majority of elected officials are still insisting the vaccines are essential and many institutions are still mandating them.
Because of this tendency, any time an alternative premise can be established which removes Western Medicine’s culpability for its failures (especially if it argues for doubling down on them), the medical community will eagerly grab them up. In the case of COVID-19, a frequently cited argument was adopted to defend the vaccines:
•COVID-19 is very dangerous (this is sometimes, but often, not true).
•There is no effective therapy for treating COVID-19 (this is not true, but because of its importance in sustaining this argument, a massive apparatus of censorship was enacted to maintain its veneer of credibility).
•Spike protein vaccines are highly effective for preventing COVID-19 (this is not true).
•The danger of COVID-19 vaccines is minuscule compared to the danger of COVID-19 (not true).
•Spike protein vaccination also protects those around you from COVID-19 (as detailed in this article and this article, this was a bald-faced lie).
Therefore, if one follows the logical conclusion of this argument, everyone must be continually vaccinated, to the point that it is acceptable to violate the human rights of individuals who erroneously believe the harms of the vaccine are greater than the benefits.
If you look at this argument without recognizing that its premises are false, it is understandable why individuals ascribing to its lies would be such zealous proponents of the vaccines. This argument is particularly challenging because many of the side effects of COVID-19 overlap with vaccine injuries (which I believe is a result of each flooding the body with toxic spike proteins), which makes it very easy for those who want to cling onto advocating for the vaccine to do so and find a way to rearrange the facts to support their biases. Two examples include:
•COVID-19 and vaccination can both cause myocarditis. This argument was used to state that the acknowledged risk of vaccination-induced myocarditis outweighed the risk of receiving a vaccine. The problem with this argument is that COVID-19 does NOT increase your risk for myocarditis, whereas spike protein vaccination myocarditis is quite frequent (also see this reference and this reference). Nonetheless, it is still frequently referenced by vaccine advocates to justify vaccination and gaslight those with vaccine induced myocarditis (e.g., one study, which fails to account for the the massive underreporting factor in vaccine injuries, is the most current one being promoted to justify this argument).
•One of the most common adverse reactions from vaccination is the subsequent development of a severe COVID-19 infection (e.g., I know multiple people who were vaccinated and within 1-2 days developed a severe COVID-19 infection and died in the hospital). This is also one of the most common causes of death linked to the vaccines in VAERS (especially the longer one is from vaccination) and dovetails with increases in COVID-19 deaths always following vaccination programs in a country.
I suspect that this phenomenon occurs because COVID-19 is largely an inflammatory disease and the immunostimulatory effect of the vaccines alters the immune response so that it attacks the host. I have also reviewed a few reports where someone who knew they were COVID-19 positive (and had minimal symptoms) received a vaccine and then immediately became extremely ill and was hospitalized.
It should also be noted that a similar issue existed with Gardasil, and in its clinical trials, it was found that individuals with a pre-existing Human Papilloma Virus (HPV) infection at the time of vaccination (HPV is linked to cervical cancer due to the chronic inflammation it creates there) caused the previously stable infection to rapidly worsen. Unfortunately, for both HPV and COVID-19, no guidance was ever issued stating that a pre-existing infection needed to be tested for, as it was believed this would reduce the ever-important vaccination rates.
As you can see from the two above examples, this is a relatively nuanced point, and if one holds onto simplistic truths to defend vaccination, it is very easy to interpret the above in a manner where the logical symbols are rearranged so that they argue for vaccination and to attribute the adverse effects of vaccination to being a result of insufficient vaccination.
“Long-Haul COVID”
The above principles are the most consequential for the discussion of long-haul COVID. Briefly, for some people who get COVID-19, after the infection clears, they essentially experience chronic fatigue and a variety of autoimmune conditions.
Many of these symptoms overlap with spike protein vaccine injury, but in most cases are not as severe and respond dramatically to treatment. For example, I have seen many cases of individuals with long-haul COVID experiencing a complete recovery after a single exosome infusion, whereas, for those with vaccine injuries, the benefit that is experienced tends to be temporary and nowhere near as dramatic, and often requires numerous sessions for a long term resolution of the disease (which matters since these infusions are quite costly).
Long-haul COVID is very much a real thing (e.g., I’ve had a few patients who developed it after COVID-19, long before the vaccines entered the market and if it’s not treated, it has a huge adverse impact on your life). This condition was initially used to market the vaccines (both to prevent you from getting it and to treat it if you had it), and I know many people now where it failed to do either (e.g., a friend and two of my friends’ patients had a slight impairment from long-haul COVID, got the vaccine and then became much less able to function). For this reason, vaccine pushers do not cite this argument as frequently now.
Many in the medical community have found one of the best ways to help vaccine injured individuals receive support is to reclassify the disease as “long-haul COVID” since this is an “acceptable” diagnosis (e.g., one that supports the COVID narrative and can receive financial compensation) and also allows the medical community to save face. Because of this, much of the most useful research I have seen on vaccine injury, including studies of the toxic spike proteins themselves, is always framed under the guise of treating long-haul COVID, (e.g., the primary study used to support my hypothesis on what was causing the blood clots from Died Suddenly) rather than treating a vaccine injury.
As a result, we now see ridiculous headlines like this in the news:
Note: One of the earlier articles I wrote on here regarding the large and tremendously costly spike in disability that was seen after the COVID-19 vaccine roll-out, which mirrors the unprecedented spike in deaths being seen by the life insurance industry. Additionally, as Igor has noted, long-haul COVID-19 is more likely to occur if a COVID-19 infection occurs close to vaccination.
As far as I know, the most definitive proof that COVID-19 vaccinations—and not COVID-19—are responsible for many of the symptoms attributed to them came from autopsies of individuals suspected to have died from vaccination. At this point many studies have detected profound inflammation that likely account of the deaths following vaccination. The most recent study for example examined 35 individuals who died within 20 days of vaccination, did a detailed evaluation for any other cause of death and excluded 10 who had potential causes of death besides vaccination. Of the remaining 25, it was determined that 5 died of myocarditis, while the other 20 had other fatal conditions commonly associated with spike protein vaccination (e.g. heart failure).
To address the question of if COVID-19 rather that the vaccine could be causing these deaths, the team in Germany that has been spearheading these autopsy studies utilized immunohistochemistry to detect the the SARS-CoV-2 spike protein (found in both the vaccines and a COVID-19 infection) and to detect the SARS-CoV-2 nucleocapsid which is only found in a COVID-19 infection but not after vaccination. As this study shows, only the spike protein but not the nucleocapsid was present, demonstrating the vaccine death cannot be attributed to a COVID-19 infection.
mRNA Persistence
I suspect the primary reasons why vaccine injuries are so much more damaging than long-haul COVID-19 are because:
•Unlike a respiratory infection, the vaccine directly enters the bloodstream which causes a variety of issues that were detailed here.
•The mRNA persists in the body and continues producing spike proteins long after vaccination.
One of the primary criteria used to approve vaccines is whether they can generate an antibody response (rather than whether they prevent disease, which generating an antibody response is not always sufficient to do). When vaccines fail to elicit this response, they are often modified in an unsafe way (e.g., the HPV vaccine is frequently linked to autoimmunity and this most likely resulted from a much stronger adjuvant being used in them as traditional ones were ineffective for eliciting an antibody response).
In the case of the mRNA vaccines, a major problem for the technology was that the body would rapidly degrade the mRNA, and as a result, the mRNA could not manufacture enough of its antigen to elicit an antibody response. To solve this problem, the manufacturers randomly added pseudouridine to the mRNA product, allowing it to resist enzymatic degradation and thereby enabling it to produce a sufficient amount of spike protein to elicit the necessary antibody response.
There were a variety of issues with this approach, one of which was that it is unclear how long the mRNA remains in the body. Since random pseudouridation was the only option available for addressing this problem, I am doubtful it was possible to precisely control the half-life of the mRNA, other than being able to ensure it was significantly extended. The only study I know of which directly assessed this question found that mRNA was still present 60 days after injection and did not assess any further into the future.
There are two other ways I know of to assess this question (there may be others too):
•The first is my own and many others’ clinical observations in the vaccine injured which suggest that new spike proteins continue to be produced months after vaccination. For example, one patient developed blood clotting after vaccination which persisted for months. At one point in time, my colleague needed to draw blood from him, was unable to (as the lines kept clotting), even when drawn from one of the largest veins in the body (the jugular vein). This was very unusual (hence why they called me about it), and we later discovered that after months of a customized proteolytic enzyme regimen (which breaks up blood clots) it was eventually possible to draw the blood again. I have also corresponded with other integrative practitioners who have reported similar issues such as needing to pull PICC lines that clotted out in vaccinated patients.
•The second way is autopsy studies mentioned before which show individuals who died from the COVID-19 vaccines had profound autoimmune responses in their tissues (e.g., the heart) months after vaccination. This autoimmune response appears to be a product of cells in those tissues producing spike proteins that coat the membranes of the cells which produced them (thus causing the immune system to attack those cells).
These studies likewise have found the presence of spike proteins in the tissues. Although very few autopsy studies have been done in this area (due to the political risks of challenging the vaccine program), we a fortunate a few brave pathologists in Germany were able to compile data to substantiate these claims
Vaccinated Blood
One of the most common questions I receive is “is vaccinated blood safe?” Many people are extremely concerned about this topic and there is a large demand for unvaccinated blood banks (which some are working to produce).
For example, recently an interesting medical ethics case emerged in New Zealand where the parents of a child who needed heart surgery that would require a blood transfusion during the operation were not willing to have the surgery unless unvaccinated blood was used. Due to the imminent risk of death that the child faced (although months later he has not died yet), New Zealand’s government has moved to revoke the parents’ guardianship of the child, and transfer it to government authorities so that they can provide the medical consent for the procedure.
The medical ethics behind overriding parental consent for a forced medical procedure are always a challenging question (e.g., I shared a very sad example here). It is particularly interesting in this case because the parents found unvaccinated donors who offered to provide the needed blood, but this request was rejected as there is no difference between vaccinated and unvaccinated blood except for vaccinated blood having vital antibodies against COVID-19.
When I looked into the basis of this claim, I found it was predicated on the assertion (or which no evidence was provided) from the New Zealand Blood Service that:
“No, any mRNA from the vaccine that is in the blood is broken down within a few hours after vaccination”
and
“The spike protein is present in vanishingly small quantities in the blood in some people for the first two weeks after their mRNA vaccine. The chance of finding spike protein in donated blood is very small, and it will be in the picogram range if it is there at all. It is not found in the blood after this time period has passed. There is no evidence that this represents any risk to recipients.”
(The tiny study I believe was the foundation for the second claim will be discussed later in this article)
To be completely honest, I have no idea if there is a problem with vaccinated blood, as like many things it just has not been tested. At this point I have seen a few concerning signs, suggesting it is the case. For example, I have read a few reports of bad reactions to vaccinated blood transfusions, and a close friend of mine had months of issues that were difficult to treat following a blood transfusion that my friend was relatively certain came from a vaccinated patient (although other factors could also have explained what happened).
I have had a long-term policy of following the precautionary principle (which states no new technology should be adopted until its safety has been proven). There are a variety of opinions on this policy (e.g., some oppose it because it impedes economic progress), but I can personally attest that following it has saved my bacon more times than I can count after something which was alleged to be safe was later proven to be dangerous.
In certain cases, you don’t really have a choice, but as best as I can, I try to pre-empt this problem (e.g., I knew there would be safety issues with the COVID-19 vaccines, so I prioritized having a method I felt comfortable using to treat it before the vaccines entered the market so I would not have to choose between the risks of COVID-19 or a vaccine). Similarly, if one plans ahead, there are a variety of alternatives to requiring vaccinated blood transfusions.
This was an issue I was motivated to investigate once I began learning of all the potential issues in transfusions, and oddly enough much of what I learned came from the fellow Jehovah’s Witnesses of a hospitalized patient I worked with (their religion forbids vaccination or blood transfusions and unlike most religions is unlikely to be challenged if an exemption is sought).
At this point in time there is some extremely tentative evidence to suspect there are safety concerns pertaining to the vaccinated blood supply, but as far as I know it is all being ignored. The Red Cross for example, who we trust for own blood supply, just passed the ball to the FDA and trusted their assessment that there are no safety issues. In addition to previous times where our government failed to safeguard the blood supply detailed by Ryan Cole, Judy Mikovits has also noted when she tried to alert the H.H.S. to contamination issues in the blood supply that needed to addressed, her findings were ignored.
Note: I am also frequently asked if it is safe to have sexual relations with vaccinated partners, and I have no idea what to say here since both me and my spouse are unvaccinated. I have seen online accounts of ultra-sensitive patients (who I periodically work with so I can appreciate their unique sensitivities to things we would typically not consider to be problematic) state they cannot tolerate being around vaccinated individuals, and I could see this issue also extend to sexual relations.
At this point in time, I only know of one example where I believe a complication appeared to have occurred and I knew the affected individual personally. A physician colleague who had avoided being vaccinated (but was frequently in close contact with vaccinated patients) asked her partner to do the same, but he ignored her advice and got vaccinated without telling her. They had intercourse later in the day, and since that time my friend has had irregular menstruation (but no other issues) she attributes to that event. If this transmission does occur, my best guess is that it occurs from the exhalation of spike protein coated exosomes.
Fact-Checking
I appreciate the fact-checkers for three reasons. The first is that they keep me on my toes (being continually intellectually challenged is one of the many things which helps prevent Alzheimer's disease). The second is that they often inadvertently promote my work. The third, and most important, is that they help me know if my argument is on target or has real issues that need to be addressed. I always question and attack each idea I consider putting forward (leading to many remaining unpublished), but my ability to do that is limited. An outside party doing the same thing is often immensely helpful and saves a lot of time.
Sometimes the fact-checks I see are not that good. For example, in my first article here, I argued that, like COVID-19, the smallpox vaccines worsened rather than improved smallpox epidemics. This then created a downward spiral as panicked governments responded to increasing smallpox cases by more and more aggressively mandating smallpox vaccinations (which was necessary as the public became aware of its severe side effects).
A massive protest eventually broke out in Leicester, an English city, resulting in mandatory vaccination being scrapped and replaced with quarantining sick patients and their contacts alongside improved public health measures. Apocalyptic predictions were made for Leicester by the medical community, but that city instead had a remarkably low smallpox incidence, and their method was subsequently utilized around the world to end smallpox.
This fact check labeled my claim as false and cited the following reasons:
However, available literature has shown that the Leicester Methods was formed by people who believed in the vaccination but recognised its limitations within a community.
You often see fact-checking statements like this which appear to disprove the central claim but in reality are irrelevant. I affirmed this statement in my essay as the local government was forced to adopt this approach after the population became unwilling to continue mandatory vaccination and used their protest to force a policy change.
The National Institute of Allergy and Infectious Diseases website has shown that vaccination was essential to eradicate smallpox.
The NIAID is the division of the Federal government run by Anthony Fauci, and somewhat understandably, like the CDC, will always claim vaccines were the greatest thing since sliced bread. The specific evidence they provided that supports the fact-checker's argument consisted of: “Through vaccination, the disease was eradicated in 1980,” which does not prove anything other than an authoritative source stating as such.
Moreover, the Center for Global Development website has again confirmed the same.
I felt this source provided the strongest arguments to support the fact-checker. It briefly described how aggressive quarantining was done in conjunction with targeted vaccination to suppress smallpox. It was possible to eliminate smallpox according to this article because:
•It had no animal reservoir
•Infections were easy to recognize early in the disease process.
•It is relatively non-contagious (this is why monkey-pox never became a thing, whereas in contrast, no amount of quarantining, including China’s imposing a draconian police state upon its citizens, which threatened its governmental stability, could contain COVID-19).
•Vaccines and natural immunity provided permanent immunity to smallpox (which I know at least with the original smallpox vaccines was a false statement).
Except for the last argument, I agreed with these points, but do not believe they prove the smallpox vaccine cured smallpox, as quarantining was likely the most important factor for controlling due to smallpox being uniquely suited to be controlled through quarantine.
From the available literature, it seems that quarantine measures, well-established before vaccination, played their part but could not have achieved eradication alone.
Interestingly, the fact checker concluded the article by acknowledging to some extent my previously labeled-as-false claim was, in fact, true. It should also be noted that although the concluding premise was asserted, nothing was ever done to substantiate that vaccination was necessary for the elimination of smallpox. Equally, my entire article discussed the original smallpox vaccine, whereas a freeze-dried formulation was utilized in the later elimination campaigns, which may have had a different effect on the recipients (many different smallpox vaccines with varying safety profiles have been developed since Jenner’s time).
Dr. Burnett
Dr. Burnett inspired the previous article I wrote on Died Suddenly with this sassy Tik-Tok critique he posted of Died Suddenly. Due to his tone, he ruffled a lot of feathers in the vaccine safety community, but I felt he did make a few valid points that needed to be discussed.
Following the publication of that article, Dr. Burnett was kind enough to share my article in his critique of it. After it was published Pierre Kory informed me over email that:
This thread is insane. It reminds me of the threads I’ve had to read trying to debunk ivermectin. It's so easy nowadays to sound somewhat smart and evidence-based while making all these pseudo-intellectual debunking claims.
I thought this over, agreed with Dr. Kory’s assessment, and realized Dr. Burnett was providing an invaluable service for highlighting critical thinking and the cognitive errors described in this article. With that in mind, let’s get to his critique!
Nothing to say here except that I suspect members of our community got under Dr. Burnett’s skin by sending my article back to him.
I have no disagreement with this because he is accurately representing my position, so I am not sure if this debunks any aspect of my article.
My reason for citing the article was because it had the only semi-detailed summary I had come across for describing their composition (as no one else wants to publish them) and thus, it had some clues we could consider in trying to elucidate what was causing the clots. I am therefore not sure if this is the most appropriate approach to take to debunking the article. However, the common way that mentally lazy people debunk opposing claims is by attacking the messenger rather than the message, as it gives them a way to quickly sound smart and authoritative without needing to make the effort to understand an opposing viewpoint, so this type of debunking is irresistible, although I feel overtly slandering The Epoch Times as a “rag” weakens, rather than strengthens Dr. Burnett’s credibility.
This is correct and why I did not heavily emphasize the article. Something I do not believe Dr. Burnett appreciates is that like other aspects of the pandemic, many laboratory owners have been asked to test the blood clots but have been unwilling to publicize their data for fear of their lab going out of business in retaliation for doing so (I know specific instances of lab owners who stated this).
In effect, this situation is not that different from the embalmers who have reported to me and my readers that they are observing these clots but are afraid to speak publicly on this issue. As far as I know, Mike Adams is the only person who has published laboratory findings on the composition of these clots, which is because he created a lab for the purpose of doing controversial analyses. For this reason, the data on the clot composition is quite preliminary, which again speaks to why I referenced the article in the manner I did.
Note: A sizeable portion of Burnett’s critique was directed towards debunking the Epoch Times article, so for length considerations, I will move to the next section of his critique
This is an accurate portrayal of my position and bears special consideration because this paper is a pivotal component of the model I am putting forward. I do not, however, agree with Dr. Burnett’s refutation of my assessment of the paper. To substantiate his critiques, Dr. Burnett cites this fact check which is 17 months old.
Like many fact checks, this article repeatedly insists there is no evidence of viewpoints contradicting the orthodox position, even though there are. In fairness, many of those studies were published after the publication of this fact check, but that does not remove Dr. Burnett’s culpability for choosing to cite the outdated article as his evidence to refute my hypothesis (which I believe came about from him reaching for something he could quickly cite to prove his point rather than an attempt to fully understand the issue). For example, this fact-check devoted a significant focus to attacking Bryan Bridle while neglecting to mention a later article that clearly supported Bridle’s position (Bridle provides a detailed summary here).
The most important study referenced in my article was then discussed by Burnett.
I believe these two posts highlight our central disagreement. The vaccines were sold to the public as being “safe” due to this modification and hence created a simplistic truth to frame the debate around the vaccines being infallible.
Note: a lot of pharmaceutical revolves around having PR firms establish similar frameworks so physicians, who typically do not question those premises, will believe they are being excellent doctors by pushing the current product on their patients.
This "safe" spike protein argument should raise some clear red flags, as many have gotten extremely ill from these experimental proteins.
To make this argument, the following is assumed:
•This modification was sufficient to prevent the spike protein’s characteristic interaction with the ACE2 receptor and is consistently present in all synthetic mRNA produced.
I have seen a lot of things suggesting otherwise, but I will give Burnett the benefit of the doubt here.
•The only way spike proteins can enter or affect endothelial cells is through the spike protein’s characteristic interaction with the ACE2 receptor.
There are a variety of other mechanisms as well. For example, the endothelium is the first tissue that will take up the vaccine (as it lines the blood vessels) and the lipid nanoparticle entry of the mRNA into the cell is independent of the ACE2 receptor (at which point, the spike protein is then produced within the endothelial cells and then expressed on their surface provoking a severe and documented autoimmune response that damages the endothelium). Similarly, the electrical charge of the spike protein directly attracts it to negatively-charged regions of the body (e.g., I believe this is how it can “do the impossible” and enter the nucleus). The endothelium, due to the glycocalyx, also contains a strong negative charge.
•Most importantly, this argument assumes that the only mechanism of spike protein toxicity is its interaction with the ACE2 receptor.
This ignores many of the other potential toxicities of the spike protein such as:
-It is able to bind heparin (which coats the protective layer of the endothelium) and then activate the alternative complement pathway on cell surfaces.
-It is highly inflammatory.
-It pathologically alters other components of the clotting cascade.
-It has homologies to a variety of tissues that appear to frequently provoke autoimmune disorders (autoimmunity is one of the most commonly observed side effects of the spike protein vaccines). One of these disorders, anti-phospholipid syndrome dramatically increases ones likelihood of severe blood clots and the one rheumatologist I have spoken to who is looking for this has told me they frequently observe it following spike protein vaccination.
-It has a prion-forming domain.
-It has a positive charge, which I have argued impairs the physiologic zeta potential and leads to catastrophic consequences. Shortly after I published that article, I was alerted by a reader to a preprint released last week provides a great deal of evidence the SARS-CoV-2 spike protein causes blood agglutination clumping due to how its charges effect zeta potential and that this may account for many of the adverse events seen after vaccination (this paper will be discussed in more detail next week).
In short, Burnett does an excellent job of illustrating why asserting a simplistic truth can provide the appearance of expertise, but in reality, completely fails to elucidate a complex subject.
The basis for this claim is a single study of 12 participants which measured the spike proteins in their blood following vaccination, where it was observed to go up, peak at 5 days, and then decline. In addition to the small sample size, there are three major issues with assuming this study’s results generalize to everything else.
The first is that no industry study has ever been performed to assess how long the spike protein mRNA persists in the body, despite this being a standard requirement for each new drug. This has been admitted in the publicly released regulatory documents on Pfizer’s vaccine (skip to Pharmacokinetics). Lipid nanoparticles containing a light-producing protein have been used to assess the distribution of the vaccine in rats, but to the best of my knowledge, no studies exist where pseudouridation was used to prevent degradation of the light producing mRNA (so it may not be metabolized in the same manner as the vaccine spike protein mRNA).
The second is that this claim ignores the mRNA persistence found in the cell study (which to my knowledge is the only study that has attempted to assess this since the mRNA vaccine manufacturers never produced the studies to answer this question which should have been required before humans received these injections).
The third is that it ignores the autopsy findings demonstrating that spike proteins that did not arise from a natural infection are present in many vaccine recipients long after their deaths.
Based on all of this, I suspect that if spike protein production were to be monitored over 6 months, the trend would differ from a brief spike and then a permanent disappearance (and may spend part of that time period in regions of the body besides the blood stream). However, as stated before, no testing of the sort was ever (publicly) done before the largest forced experiment in human history.
A minor point to mention here is that in the study I referenced, they tested 100,000 pg/mL, 50,000 pg/mL, 10,000 pg/mL, and 1000 pg/mL concentrations of the spike protein. 1000 pg/mL was sufficient to cause a significant occurrence of these misfolded fibrin clots, and no lower concentration was tested. It is thus quite possible that a lower concentration approaching the 68 pg/mL level would also be sufficient to elicit similar effects.
This perfectly demonstrates the unfalsifiability of Western Medicine discussed above.
Here, Burnett is referencing the study I cited, which to my knowledge, is the only article which evaluates how long the mRNA persists in the body.
Burnett’s refutation of this article has two central issues:
•It was cited to demonstrate that mRNA does not disappear within hours as claimed by the authorities. His critique does not in any way disprove this response.
•You cannot state this is a perfectly normal response to a vaccine because there is no past precedent for the behavior of an mRNA vaccine or what constitutes a “perfectly normal immune response” to pseudouridated mRNA.
When I read this, I felt that this was the strongest argument Burnett raises to refute my hypothesis so I took his critique into consideration and had an in-depth look at it.
To address his first point, I believe the reason that this was seen in France was that Luc Montagnier is one of the only researchers alive who would be willing to publish research like this which exposed him to such significant professional risk. Given that I had never heard of anyone discussing someone developing CJD before the COVID-19 vaccines, and I now know of three people, I am somewhat inclined to believe an increase has occurred.
In regards to the databases in question, if we were to assume that my observations of the increases were valid, the discrepancy is either an issue of under-reporting (e.g. researchers were afraid or unwilling to report it) or not enough time has elapsed to observe this (e.g., the CDC’s data only goes back to 2020 and Europes’ global CJD surveillance network, which tracks 29 countries, also only goes back to 2020). At this point, the only dataset I’ve been able to find which includes the years where vaccines have been on the market is Canada’s (which does support Burnett’s assertion that no increase is occurring), so I am unsure how they were able to claim an increase is being observed following vaccination as the data does not appear to exist.
When I read the fact-check that Burnett cited, I realized that many of the necessary references were missing (hence, why I had to look for the databases myself), and it instead defaulted to common tropes like “The CDC, and certainly the British who have very rigorous vaccination surveillance systems have not found an increase in Creutzfeldt-Jakob disease,” “correlation is not causation” for the case reports. They also of course emphasized that “none of these articles were peer-reviewed” (which at this point primarily functions to prevent controversial hypotheses from being discussed).
I did a quick look on open VAERS (search for “Creutzfeldt”) and discovered from 1990-2020, a total of 12 cases of CJD had been reported most of which did not have causation asserted by the reporter, whereas in 2021, 33 cases were reported, and 40 have thus far been reported in 2022. Of these 73 cases, most expressed that CJD resulted from the vaccine, and 72 were listed as being from a COVID-19 vaccine, while one was listed as unknown (but had a Pfizer COVID-19 lot number). Given this, I am unsure if the fact-checkers statement regarding the CDC’s monitoring is accurate, as between 0-1 cases of CJD should have emerged in VAERS but instead 73 did (remember only one in a million people are supposed to develop CJD per year which).
This was the part of Burnett’s fact check that I most disagreed with, as he effectively stated “instead of making the effort to review Fleming’s case, I am going to attack his character so I can maintain a veneer of authority here without having to make the effort to understand Fleming’s claims.” In some cases, if you do this, it doesn’t really matter because the evidence being provided is of poor quality; however, since Fleming produced a very compelling body of evidence to support his argument, I believe that Burnett is at fault for taking the intellectually lazy path here.
Outside of that, this issue touches upon two larger issues. The first is that selective prosecution is a major problem within our judicial system as individuals who align with vested interests and commit egregious violations are rarely if ever prosecuted, whereas those who oppose them are often prosecuted for relatively minor violations.
This is a major issue with Medicare, where there are many examples of individuals committing egregious healthcare fraud that hurts many individuals being given a pass for years if not decades. Conversely, individuals in the integrative medical field frequently find themselves exposed to costly (and potentially career-destroying) audits for minor paperwork errors.
Because of what they have seen happen to others, every single integrative practitioner I know refuses to take Medicare (with the exclusion of one who designed their practice for Medicare and does not offer many other vital services to patients) because they cannot afford to take on the risk that receiving Medicare entails, which makes vital health care unavailable to those who lack wealth. I listened to Fleming’s account of his crime (which could certainly be biased), and from that, I do not believe his offense in any way justified suspending his license, but again illustrates why it is so challenging to take Medicare as a provider who bucks the system.
Secondly, any physician who speaks out against medical orthodoxies (e.g., vaccines, using repurposed drugs to treat COVID-19) takes on an immense risk. They frequently have to worry about being fired from their place of employment, being blacklisted for future employment (this also happens to other whistleblowers, such as those within the pharmaceutical industry), losing their medical licenses, losing their board certifications, and in some cases, being targeted with physical violence. I have observed this throughout my entire career, and have found most of the well-intentioned physicians who challenge medical orthodoxies do so covertly rather than overtly (much of my success during my medical training came from identifying these individuals, who are everywhere, and them graciously offering their support to my work).
In most cases, this results in physicians who speak out against prevailing orthodoxies being those at or near retirement because they can afford to be professionally dismantled (I highly respect Pierre Kory because he is an exception to this rule who, for some reason, was compelled to speak out and bear the risk that it entails at the prime of his career). In addition to physicians near retirement, the other demographic who frequently speak out are those who were already canceled for something else (e.g., Paul Marik), and thus have much less to lose by speaking out. While I feel that what happened to Fleming was unfortunate, it was also a blessing for the vaccine safety movement as he was a uniquely qualified expert to assess this issue (M.D., J.D., Ph.D., Cardiologist, journal editor, with an extensive background in inflammation and blood clots).
I am in complete agreement with Dr. Burnett here.
I am also in complete agreement with Dr. Burnett here.
I sincerely hope this final Tweet serves to effectively illustrate many of the points I have shared throughout this series, and I sincerely thank Dr. Burnett for candidly revealing his internal thought process (some of which I agree with). I also must thank him for a relatively fair-fact check (compare it to this one Kirsch recently reviewed) and for not attempting to debunk or attack aspects of my argument, which fall completely outside his knowledge base (e.g., the discussion on colloidal stability and microclotting).
Conclusion
Many are understandably upset with Dr. Burnett and have published pieces attacking him. I am reluctant to do so because I believe his ideas and not his character should be attacked. Additionally, I frequently deal with physicians like Dr. Burnett, who are caught up in the mass formation psychosis of the medical orthodoxy, and I have dealt with many far more upsetting individuals.
In this series, I attempted to make the case that critical thinking has been replaced with a pseudo-education that gives the appearance of intelligence but in reality creates standardized cognitive patterns which are programmed to arrive at conclusions supporting the vested interests which fund that education. One of the most common standardized patterns you observe is an algorithm that seeks to rapidly identify “authoritative sources” and then string them together until a configuration can be arrived at which defends the status quo (e.g., consider how often Burnett focused on the source rather than its evidence).
In a recent article, I detailed how creating compromised “impartial” authoritative sources is a cornerstone of all propaganda and that all industries default to this approach because it is frequently cheaper for them to create the perception that they are acting in good faith than it is to conduct their business in a manner the public would want to support
In this series, I hope I have been able to establish how the educational system must be structured to support this technique. Going forward, I do not wish to engage in additional fact checks or debates over who is right, as this is a time-consuming process and it is quite likely that any future articles will be made redundant by the content within this series (as the flaws in how we teach critical thinking are unlikely to change in the near future). However, at the same time, I do feel obligated to maintain the accuracy of my work and will update the articles as errors are sent my way.
As I conclude, I want to highlight how many lies can be packaged into a simple series of widely held but largely unchallenged assumptions. Since the public at large feels very strongly in this subject, countless highly motivated researchers dug up much of the evidence necessary to disprove these orthodoxies (hence why I am able to produce pieces like this) and the interest is present for the public to learn about it (hence why you will read it).
Sadly, COVID-19 is by no means the first time this has happened, and I can think of many other medical topics which were inaccurately portrayed at the behest of pharmaceutical interests and for the most part have remained unchallenged. Many of those other stories comprise a key aspect of the “Forgotten Side of Medicine” and it is my hope that you will help me to make it possible to reveal some of them.
Source: The Forgotten Side of Medicine
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