What Can Megyn Kelly’s Adverse Vaccine Reaction Teach Us?

There were three highly unusual characteristics of the COVID vaccines:

• From the start, they were highly controversial and opinions on them largely split along partisan lines.
• Despite the previous, they were eventually mandated upon the entire population.
• The vaccines had an unprecedented degree of toxicity, to the point so many were injured that the majority of the population is worried about their side effects, almost half of vaccinated American adults believe they suffered an adverse reaction, and half of America believes the COVID vaccines are causing a wave of unexpected deaths.

This in turn has understandably shaken the lifelong trust many Americans held in our institutions and also has created a tragic political situation for the vaccine injured. Since the left strongly endorsed the vaccines, admitting you had an adverse reaction is a direct affront to their tribe. As a result, many liberals I’ve talked to have told me they’ve had to stay silent about their injury or risk being excommunicated.

Likewise, in the medical field, because the faith in the vaccines was so powerful, stating you had an injury was viewed as being equivalent to medical malpractice since it might encourage others not to receive the “life-saving” COVID vaccine. For example, a California doctor who has treated thousands of vaccine injured patients frequently saw local nurses only discover their co-workers had also been injured because they met each other in his waiting room.

The psychological burden vaccine injured people in those industries face is thus hard to put into words — their bodies and lives are falling apart, no one can tell them what to do (or even how to fix it) and if they speak publicly, they risk economically blacklisting themselves. As a result, I know of many VIPs and celebrities who are vaccine injured and are being treated in private but are not going public with it as they are afraid of losing their careers.

Similarly, for those working in the media (which is largely funded by the pharmaceutical industry), regardless of what they see happening to themselves, their friends or their families, they can’t speak out on the issue because of the professional risks they face for doing so. As a result, the only news hosts I know who have spoken out against the vaccine are those who left the networks to build their own platforms.

Note: The one exception I know was Tucker Carlson — who was fired immediately after giving a scathing critique of the vaccine campaign and the media’s complicity in it. Since then on Twitter, he built one of the largest independent media platforms in the world, and has increased his criticism of the vaccines (where amongst other things he stated he never got vaccinated).

For example:

Vaccines and Autoimmunity

The adaptive immune system works by producing lots of white blood cells with a random protein sequence on them, and then waiting until a foreign protein (henceforth termed an antigen) comes into contact with a white blood cell whose random sequence matches the antigen.

Once this occurs, a signal is set off for the white blood cell to copy itself, and large numbers of white blood cells matching that cell form which can then bind to the new antigen and thereby protect the body from it.

While this approach has served our species well, it’s not perfect because it takes time (the right cell has to stumble across the antigen), and sometimes the needed adaptive response doesn’t form at all. The theory behind vaccination is that since infectious microbes continually reproduce inside the body, by the time an adaptive immunity forms, the infection may have progressed too far and your immunity can no longer save you (or it does but the disease you go through will be much worse).

Vaccines work by introducing one or more of the antigens from the microbe to the body and allowing you to develop an adaptive immunity to it so that when the actual (reproducing) microbe enters your body, your adaptive immunity can kick into gear before the microbe overwhelms the body. While this sounds good in theory, there are a variety ways where it runs into issue in real life.

One of them arises from the fact that for vaccines to be approved, they have to reliably stimulate an adaptive immune response to their antigen. In order for that to happen, vaccines either need to directly inject a lot of the antigen or cause the antigen to reproduce inside the body (e.g., the measles vaccine is a replicating virus), so that in either case, enough of the vaccine antigen can come into contact with the immune system for its adaptive process to occur.

Since antigens are expensive, it’s often not commercially feasible to produce enough of them for an injection to generate the desired immune response. To solve this problem, vaccines are often mixed with adjuvants which stimulate the immune system into responding to the nearby vaccine antigens. Furthermore, some antigens are more difficult to elicit a reliable response from (the ones from HPV being a classic example) and in turn require even stronger adjuvants to be used.

A major problem with provoking the immune system to produce an immune response to the vaccine antigen is that it can trigger an immune response to other antigens as well — such as those the body needs to function. For example, one study showed that mice developed allergies to pollens that were in the air at the time of their vaccination.

This becomes more of an issue when antigens in vaccines partially match those in human tissue. For example, the hepatitis B vaccine has a significant overlap with myelin (which coats your nerves and thereby allows the nerves to function).

Because of this, debilitating demyelinating disorders (e.g., multiple sclerosis) have been associated with hepatitis B vaccination, and one study showed approximately half of its recipients also developed immune reactivity to myelin (which in the majority of cases persisted for over 6 months).

Since autoimmunity is a longstanding issue with vaccines, an excellent textbook has been written compiling the numerous autoimmune disorders known to emerge from each vaccine due to the specific makeup of their antigens. Likewise, many have suspected the epidemic of autoimmunity in this country is due to increasing childhood vaccinations as:

• Autoimmune disorders are dramatically lower in unvaccinated children (e.g., see this study and this study).
• The rise of autoimmune (and allergic) disorders in this country has directly paralleled the rise of the number of required vaccinations.

Note: Many, but not all, of the disorders listed in the study cited above are autoimmune in nature.

Theoretical Risks of Autoimmunity

When the mRNA vaccines were being developed, a few major concerns emerged scientists tried to sound the alarm on, but were nonetheless ignored. One of those was that the vaccine design had a high risk for autoimmunity. This was because:

So, given all of this, you might think that the regulators would have been quite concerned about the potential autoimmune risk of this technology. However when I read through leaked regulatory documents between Pfizer and the EMA (Europe’s FDA), I noticed that very little was done to evaluate autoimmunity and this did not appear to be a priority for the EMA.

“Thus, vaccination with modRNA is expected to induce robust neutralising antibodies and a concomitant T cell response to achieve protective immunity. Nevertheless, no further discussion was provided regarding the possibility of autoimmune responses induced by the ModRNA.

The Applicant is invited to further discuss the risk that the mRNA vaccine can trigger potential autoimmune responses and how they plan to possibly evaluate their occurrence.

Safety pharmacology programme. No safety pharmacology studies [a more detailed form of toxicology] were conducted with BNT162b2. The Applicant refers to that they are not considered necessary according to the WHO guideline (WHO, 2005). In addition, no findings on vital organ functions have been recorded in the repeat dose toxicology studies. Thus, the absence of safety pharmacology studies is accepted.

Although it is difficult to provide clear cut numbers as it depends on the sought outcome, as a general principle the ETF agreed that for reactogenicity it would be sufficient to test around 300 subjects per age stratum.

Serious rare events could be disproportionately represented in children vs. adults e.g. narcolepsy [this was an issue with the 2009 swine flu vaccine] or other autoimmune disorders that are more likely to occur in adolescents than adults.

However, such events would require sample sizes larger than 30,000 individuals to be able to detect anything. As this would be unfeasible, especially for a paediatric study, we need to rely on post-authorisation surveillance.”

All of this is similar to how they gave Pfizer a pass on evaluating if the vaccine would cause cancer, which, leading into the vaccine rollout was understandably one of the largest concerns with an experimental gene therapy.

“Genotoxicity — No genotoxicity has been provided. The components of the vaccine formulation are lipids and RNA that are not expected to have genotoxic potential. That being said, the novel lipids possess an acetamide moiety which is classified as possible human carcinogen (IARC Group 2B) with debated genotoxic mechanism, which should be discussed further.”

Note: Regulators also oddly failed to require the vaccines to be sufficiently tested for their effects on fertility the other major concern with the vaccine — a subject Arkmedic has done great work to expose.

Experiences With the Vaccine

Since I knew a lot of people were going to ask me about the vaccine, I did my best to research it before it was released.

From doing so, I gradually came to suspect that the failure to test the vaccine’s greatest theoretical risks meant it was very possible issues had been already been discovered and that the manufacturers then decided it was better to just not officially test them so the regulators would not have a reason to veto their application and plausible deniability would exist once the adverse effects were eventually discovered.

In turn, I concluded the most likely problem with this vaccine would be chronic complications (e.g., cancer) that took a while to show up and would only be recognized once everyone had long since been vaccinated. As the vaccine started to hit the market, three red flags jumped out at me:

• All of the PR and marketing stated that if you felt awful after the vaccine, that was a good thing and it meant the vaccine was working. I had never seen a vaccine be presented in this way by the media before.
• Pfizer’s study (which was published shortly before the vaccine got approval) had a rate of acute adverse effects which was dramatically higher than I’d seen with any other vaccine (e.g., 59% experienced fatigue from Pfizer’s vaccine, whereas around 10% – 15% experience fatigue after an influenza vaccine).
• Many of my colleagues (who were first in line to receive the vaccine — something I suspect was done to market it to the general public) reported feeling absolutely awful after COVID vaccination.

All of this suggested that the vaccine was extremely effective at provoking the immune system, and given the other issues, that autoimmunity was a real risk of the vaccine.

Once the vaccine entered my community (it took a bit longer to get into my corner of the midwest), I immediately began to have a lot of patients show up with issues from the vaccine. A few things were very striking about what I heard:

• Patients said they had never had a similar issue with any other vaccine (e.g., their annual flu shot).
• Areas of pre-existing immunity flared. For example, joints that for years had occasionally experienced an aching arthritis suddenly felt as though they were on fire. Likewise, old injuries and scars suddenly began to flare and hurt greatly (something I had previously learned to associate with severe inflammatory conditions like Lyme disease).
• A variety of other symptoms were reported which I gradually concluded could be linked to either an inflammatory process or microclotting.

Note: I also began seeing very similar symptoms to what my patients were reporting on a variety of online forums. This recent posting is the most comprehensive summaries I’ve seen of those reports.

Seeing this made me very uneasy, as I felt that if I’d underestimated the vaccine’s acute reactions to this degree, it meant I’d likely greatly underestimated the chronic ones as well.

Before long, I started having more and more friends from around the country reach out to me sharing that someone they knew had died suddenly after the vaccine (most frequently from a heart attack) and wanting to know if it could be linked to the vaccine.

At that point I realized I needed to start documenting everything being reported to me (which essentially matched what I was seeing reported online), and a year later I published that compilation, which went viral and made this Substack become part of the vaccine safety debate.

Note: After the vaccines were launched, I also began to hear unusual reports of heart attacks from my colleagues I’d never heard before, but it didn’t occur to me they might be linked to the vaccine until my I started hearing the reports from my friends.

At this point, I began to suspect the primary issue with the vaccines would be autoimmune in nature and or due to the previously mentioned alterations of physiologic zeta potential which led to complications like microclots.

To investigate this, I started contacting rheumatologists and neurologists I knew to find out if they were seeing anything unusual (these would be the two specialities most likely to have patients show up with challenging autoimmune conditions).

A few privately confided that something was amiss, but most did not seem open to the possibility there were potential issues with the vaccine and instead kept going back to COVID-19 having a high risk of causing a wide range of complications like autoimmunity.

I then tried a different tactic and contacted medical students and medical residents I knew to find those who were rotating under a neurologist or rheumatologist. I received more candid answers from them; many believed they were seeing far too many patients reporting autoimmune complications from the vaccine.

I then decided I needed to find the time to shadow one of these doctors and was able to do so with rheumatologist.

What I saw was very striking — it seemed that around 25% – 30% of her patients (some of whom were my coworkers) had either developed a new autoimmune condition after the vaccine or had a long existing (and stable) autoimmune condition become much worse (e.g., one was hospitalized and didn’t remember most of the hospitalization), and frequently required the rheumatologist to change them to a stronger medicine.

Simultaneously, I also began to see unusual autoimmune conditions in my co-workers and social circle (e.g., multiple cases of ALS — something which typically affects only 1/50,000 people per year). One of the most telling stories happened at the very start of the rollout when a close friend received the Moderna vaccine and developed polymyalgia rheumatica (this condition typically emerges in 1/1900 people over 50 each year).

I found her story noteworthy because when she saw her rheumatologist, she was told he’d already seen quite a few other patients who developed PMR following Moderna.

Note: I also saw certain autoimmune conditions which appeared to have a delayed onset after the vaccine. This started after I began receiving consultations for multiple sclerosis and noticed they were all either cases that had long been stable and then gradually worsened after vaccination or new ones that emerged months afterwards. After investigating more, I found quite a few other physicians who were also seeing the same thing.

Oddly however, despite a great deal of evidence linking the vaccine to autoimmunity, I have thus far only come across one doctor who was willing to publicly acknowledge this:

When I asked Pierre Kory about this (who specialized in treating vaccine injured patients) he shared that:

“I think autoimmunity is one of the key pathologies that underlies many of their symptoms but they don’t always meet the classic criteria for a specific autoimmune disease with the standard autoimmune panels, although more specialized autoimmune tests consistently detect a wide range of auto-antibodies.”

Note: The other key pathology is pervasive microclotting. Additionally, one common autoimmune disorder which frequently follows vaccination is antiphospholipid syndrome, a very rare condition known to dramatically increase one’s risks of blood clots, infertility, strokes and heart attacks. I believe this risk is at least partly due to cell membranes (where the spike proteins end up being seen by the immune system) being largely composed of phospholipids.

The Data on Vaccine Autoimmunity

Numerous datasets exist suggesting there is a high risk of autoimmunity from the vaccine. These include:

I must emphasize that these are all massive and unprecedented increases. The only two pharmaceuticals I can think of that had a similar ability to create autoimmunity were the HPV and anthrax vaccines.

Conclusion

While I feel terrible for Megyn Kelly’s adverse reaction, I hope that this article serves to illustrate that her development of a new autoimmune condition was not all that uncommon and that doctors should have been aware of these risks before they pushed their patients to vaccinate (especially for patients with a tendency to autoimmunity due to pre-existing autoimmune disorders).

Sadly the opposite happened, and those with pre-existing autoimmune conditions were instead told it was urgent for them to vaccinate since they were immune suppressed and at a higher risk of getting COVID-19.

One of the things that’s difficult to appreciate about autoimmune conditions (unless you have one) is just how incredibly impactful and debilitating they can be for one’s life. For example, my friend who developed PMR couldn’t function for months and two of the doctors I worked with when the vaccines were introduced suffered debilitating (and life-threatening) complications which caused them to have to leave the facility because they simply could no longer work.

Ed Dowd and his team has been attempting to quantify the economic impact of these injuries. Large numbers of life insurance claims filed (for sudden deaths) and large numbers of people exiting the work force due to vaccine induced disability have massive costs to the society, and most importantly, these costs are big enough to threaten the profits of upper class (which may in turn motivate those in power to fix the problem).

Dowd’s (conservative) estimate was that 18% (26.6 million) of the American workers who received the vaccines were injured, 0.93% (1.36 million) were disabled, and 0.05% – 0.1% (300 thousand) died. One database they identified, which shows England’s monthly disability clearances sorted by the cause of the disability helps to illustrate how vaccine injuries are affecting from the workforce.

Specifically, when compared to the existing trend prior to the vaccines being introduced, autoimmune conditions resulting in a disability approval increased by between 100% – 400% (depending on the condition). This represents 4-10 standard deviations from the mean, something that is statistically impossible to have happened by chance.

Note: The specific autoimmune conditions in England’s dataset were lupus, vasculitis, Sjogren’s, antiphosopholipid syndrome, systemic sclerosis, “other autoimmune diseases,” and “other diseases of the immune system.”

Having worked in the disability approval process, I can share that it is quite hard to get disability, and that the majority of people seeking disability sincerely wish they could work instead. While my experience is in only in America, I suspect a similar situation exists in England, which again underscores the immense human cost of the COVID vaccine’s autoimmune complications.

A Note From Dr. Mercola About the Author

A Midwestern Doctor (AMD) is a board-certified physician in the Midwest and a longtime reader of Mercola.com. I appreciate his exceptional insight on a wide range of topics and I’m grateful to share them. I also respect his desire to remain anonymous as he is still on the front lines treating patients. To find more of AMD’s work, be sure to check out The Forgotten Side of Medicine on Substack.

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