COVID-19
The Tragic Story Of A 14-Year-Old Vaccine Myocarditis Victim — One Of Umpteen Males Misinformed By Health Authorities
Posted with permission from the author, this was originally published in Noble Truths with Rav Arora
Vaccine myocarditis is not trivial, mild, or “rare.” In young men, it’s a far greater risk than Covid hospitalization and death.
Read Part 1 and Part 2 of my investigative vaccine myocarditis series.
On May 12th of last year, school teacher Emily Jo took her 14-year-old son Aiden to get his first Pfizer vaccine dose. The public health authorities and her son’s pediatrician unanimously recommended vaccination, prompting her decision. She knew that mRNA shots caused some number of adverse events, like all vaccines, but was re-assured by the CDC and White House’s public recommendation.
“The talk amongst the mainstream medical community was that vaccine myocarditis was mild and that this was very rare,” she told me.
At that time, despite alarming heart inflammation reports from Israel, the CDC publicly claimed to have found no signal of myocarditis after “intentionally” investigating over 200 million administered doses.
Moreover, Emily Jo was never warned of the myocarditis risk or informed about the risk-benefit profile.
“When I took Aiden to get his vaccines at the drive-through vaccination site, there was no warning about myocarditis. We were not counseled about any side effects to be aware of,” she said.
In the name of public safety, scientific innovation, and personal health, Emily Jo sent out a celebratory tweet proclaiming she and her family are “so thankful” their teenage son was able to get vaccinated.
However, her pride and relief turned out to be tragically short-lived. Two days after her son’s second vaccine dose (which he got a month after his first), he ended up in the hospital after experiencing intense chest pain. He was moved to a room on the acute cardiac floor where he was found to have elevated troponin levels (a key sign of heart damage) and an abnormal electrocardiogram. Every doctor Emily Jo spoke to at the pediatric hospital Children’s Healthcare of Atlanta confirmed her son had vaccine-induced myocarditis.
Given her son’s dire condition, Emily worried Aidan might die or suffer from a catastrophic injury. Thankfully, after four distressful days at the hospital, Aidan troponin levels returned to baseline and he was discharged. However, this didn’t mean he could return to his normal life. Aidan was unable to do physical activity for six months. Sports, hikes, and other forms of exercise were deemed too dangerous for his heart — a typical consequence of myocardial injuries.
“I had no idea how life altering ‘mild’ myocarditis actually is. I have a very hard time with the label ‘mild’ for anything that requires hospitalization and months of inactivity,” Emily Jo said.
The most serious concern with Aidan’s vaccine injury isn’t the harrowing experience itself, but the frequency at which it occurs. Virtually any substance or medication will produce a diverse range of reactions across the human population. As Sam Harris has correctly noted, if you administer peanuts to everyone, there will be some number of fatalities and cases of anaphylaxis.
The rare incidence of life-threatening anomalies doesn’t mean that peanuts produce a net harm or should be banned altogether. Tragic interactions with any kind of externality are often exaggerated and exploited to justify irrational ideological agendas. For example, Minneapolis officer Derek Chauvin’s treatment of George Floyd paved the way for radical “Abolish the Police” initiatives.
In the case of COVID-19 vaccines causing myocarditis, we aren’t dealing with trivial ratios of one in a million or even one in ten thousand. Among the most robust data we have—according to Dr. Tracy Beth Hoeg (Florida Health department) and Dr. Marty Makary (Johns Hopkins University)—is from Dr. Katie Sharff (who had her young son vaccinated) and colleagues, who analyzed a wide database from Kaiser Permanente.
Dr. Vinay Prasad on the Kaiser Permanente study
Going beyond other study methods, Sharff found a number of vaccine myocarditis cases that weren’t explicitly labelled as such or were outside the parameters of the CDC’s vaccine safety search. After performing an exhaustive search of the Kaiser medical records, Sharff and colleagues found a 1 in 1,862 rate of myocarditis after the second dose in young men ages 18 to 24. For boys ages 12 to 17, the rate was 1 in 2,650. Countries with active surveillance monitoring of medical data (which suffer from far less under-reporting than the passive system in the U.S)—such as Hong Kong—show virtually identical figures. The risk of vaccine-induced myocarditis remains elevated for men up to the age of 40.
11:26 PM ∙ Jul 19, 2022
One need not be an anti-vaccine conspiracy theorist to recognize these figures are alarmingly high.
Historically, vaccines with adverse event profiles far lower — but still deemed far too high — than the mRNA myocarditis signal have been withdrawn. The 1976 swine flu vaccine was pulled back because of a 1 in 100,000 risk of Guillain-Barre Syndrome.
An approximate 1 in 3,000 risk of vaccine myocarditis in young males would only be favorable in a cost-benefit analysis wherein the risk of disease would be considerably serious.
The pre-vaccine Covid infection fatality rate for people under 30 was 0.003%.
The vaccine myocarditis risk after dose two (0.03%) is ten times higher than the fatality rate.
Today, since the vast majority of young Americans have been previously infected with Covid once or twice, the calculus has shifted. Putting aside the question of whether it makes sense for unvaccinated people to get the primary series targeting outdated variants, the myocarditis risk (in young males) from even one dose eclipses that of hospitalizations from re-infection. Josh Stevenson — a data analyst who has co-authored multiple peer-reviewed studies on vaccine myocarditis — has designed the following bar graph comparing risks:
Using Covid hospitalization statistics instead of deaths is a more accurate comparison since Covid deaths are virtually nonexistent in healthy, young populations. Still, the differences are massive. For example, the risk of myocarditis from dose one in males ages 18-24 is 15 times higher than hospitalization from Covid re-infection. For dose two, the risk differential is a stunning 61 times greater.
Unless a young male is immunocompromised, obese, or suffering from other serious health conditions, taking any mRNA Covid vaccines carries far more risk than benefit. The best data indicate this is a fact — though this is hardly considered in mainstream media.
***
Cases such as Aidan’s have prompted many honest voices in the public health community to reflect on the CDC’s top-down vaccine recommendations. Dr. Anish Koka—a renowned cardiologist with his own clinic in Philadelphia—believes medical experts should have been “more careful about recommending this to low-risk patients from the very outset.”
Koka Cardiology
As he explained to me over email, “Clinical myocarditis is never mild—a recent paper of 12–29-year-olds found 25% of myocarditis patients end up in the ICU, and 1 patient needed ECMO (a modified heart lung machine) to stay alive.”
“The long term impacts of the persistent scars that are apparent in follow-up on cardiac MRI are also unknown,” he added.
Koka believes it was “apparent by April (of 2021) there was a real safety signal,” and he questions why public health authorities “didn’t make decisions starting then to at least inform the public about this potential side effect at that point. ”
Instead of mitigating risks by further spacing vaccine doses, recommending Pfizer over Moderna, and being honest about near-zero risks of severe outcomes in younger, healthy groups, Big Pharma in collusion with the government recklessly opted for universal decrees.
Looking back on the CDC and Food and Drug Administration’s (FDA) possible negligence and recklessness, Khoka stated the harm perpetrated was “unconscionable.”
More and more medical professionals are now speaking out on the strong likelihood that vaccine-induced myocarditis seems to occur at a rate that far exceeds deaths and hospitalizations in healthy, naturally immunized men under 40. Johns Hopkins public health professor Marty Makary recently wrote in a tweet:
“Last y[ea]r, the NEJM described a 22-yr-old that died from vax-induced myocarditis & I’ve heard of many more cases. I have never heard of a young healthy person with nat[ural] immunity dying from Covid. Our gov’t doctors have not been honest about the risks:benefit in young healthy people.”
2:00 PM ∙ Sep 27, 2022
I had been frankly hesitant to make such a statement since it isn’t scientifically rigorous, but since this topic is becoming less taboo, I will say it now: I have heard (without deliberately seeking) of several vaccine myocarditis cases in healthy, young people but have heard of zero hospitalizations and deaths.
This observation is in line with real-world statistics. According to UK databefore Omicron—when the virus was deadlier—the COVID-19 death rate was just over 0.001 percent in unvaccinated 30-year-olds. For unvaccinated people in their 20s, the risk was more like 0.0001 percent. Hospitalization figures (from, not with COVID-19) are similarly infinitesimally low. Compare that with a vaccine myocarditis risk of 0.03 percent in young men.
It makes little coherent sense why young males were not only permitted and recommended to get the mRNA vaccine series, but mandated by the state (as I wrote at length here). This injustice is even more egregious now that we know vaccines confer little to no long-term protection against infection.
Aidan’s mother recently came across a new scientific paper showing dismal vaccine efficacy in adolescents and tweeted the following:
Thinking about the fact that Aidan got myocarditis for 30.6% transient efficacy is pretty infuriating…This Pfizer vaccine was initially sold as 95% effective. Big change.
Fast-forward to today, Aidan is far from his physical condition before getting double-vaccinated. After advising him against even going on for a walk for the first four months post-vaccination — and eventually allowing a return to exercise after six months — Aidan’s cardiologist has cleared him for all physical activity. However, “he tires more easily and has lower endurance,” Emily says.
“He used to be able to run around and play for hours….now it’s like 20-30 minutes and he gets exhausted,” she added.
More than a year later, Aidan is still recovering from a vaccine that had little to provide him in the first place. Though some have shamed Emily for getting her son vaccinated, she is hardly to blame for trusting in taxpayer-funded health agencies whose sole function is to keep the public healthy and safe.
In light of the FDA and CDC’s outrageous push to vaccinate everyone with the new “bivalent” booster—despite explicitly “unknown” myocarditis risks—hopefully more people will wake up and re-evaluate their blind faith in institutions who have far abandoned their ostensible mission of keeping us safe and healthy.
Rav Arora is a 21-year-old, independent journalist formerly writing for top publications such as The Globe and Mail and New York Post before critically covering vaccines and state mandates. Please consider supporting his fearless journalism, focusing on tragic stories of vaccine myocarditis, by becoming a paid subscriber. Read his in-depth vaccine myocarditis series here.
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Thank you for reading Noble Truths with Rav Arora. This post is public so feel free to share it.
Brownstone Institute
The Trump Administration Must Bring Moderna to Heel
From the Brownstone Institute
Moderna’s European filing also revealed that the company withheld trial results demonstrating that children under 12 who received the vaccine were ten times more likely than those who received the placebo to suffer “serious side effects.”
Last week, independent journalist Alex Berenson reported that a preschool-aged child died of “cardio-respiratory arrest” after taking a dose of Moderna’s Covid mRNA vaccine during its clinical trials. Despite federal requirements to report all trial information, the company withheld the truth for years as it raked in billions from its Covid shots.
The extent of the cover-up remains unknown, but Moderna, headed by CEO Stéphane Bancel, disregarded federal law requiring companies to report “summary results information, including adverse event information, for specified clinical trials of drug products” to clinicaltrials.gov. The company, not the government, is responsible for posting all results, and failure to report the death of a child constitutes a clear breach of US law, which threatens civil action against any party that “falsifies, conceals, or covers up by any trick, scheme, or device a material fact.”
To this point, pharmaceutical companies have remained largely immune for their role in perpetrating globally-scaled deception resulting in thousands of vaccine injuries and billions in profits. They have enjoyed a liability shield courtesy of the PREP Act, which offers protections for injuries resulting from vaccines; that indemnity, however, does not extend to non-compliance with federal regulations, material misstatements or omissions of fact, or other offenses.
The death of the child only became known because of an obscure European report released last year, which revealed that Moderna has known about the death for over two years while it continues to advertize Covid shots to children as young as six months old.
Moderna’s European filing also revealed that the company withheld trial results demonstrating that children under 12 who received the vaccine were ten times more likely than those who received the placebo to suffer “serious side effects.” Without any evidence, Moderna claimed that the side effects, including the death of a child, were unrelated to the shots.
The incoming Trump administration offers a rare opportunity to hold pharmaceutical companies accountable and to investigate the depth of the cover-up.
The FDA is responsible for enforcing the reporting of vaccine trial results, but recent heads of the agency such as Scott Gottlieb and Robert Califf have been fanatical supporters of Big Pharma. Trump’s choice for FDA, Dr. Marty Makary, presents a stark contrast to his predecessors. Makary has criticized the US Government’s reluctance to acknowledge the role of natural immunity in preventing Covid infection, and he opposed the widespread vaccination of children. He testified to Congress, “In the U.S. we gave thousands of healthy kids myocarditis for no good reason, they were already immune. This was avoidable.”
President-elect Trump has tapped Robert F. Kennedy, Jr., perhaps the most well-known critic of the Covid vaccines, to lead the Department of Health and Human Services, which oversees the FDA. He has named Dr. Jay Bhattacharya, an author of the Great Barrington Declaration, as his choice to head the National Institutes of Health. Further, Senator Ron Johnson (R-WI) told Berenson that he plans to subpoena the FDA once Republicans become the majority party in the Senate this month.
President Trump’s first term was ultimately defined by his failure to fulfill his pledge to “drain the swamp.” A corrupt bureaucracy, personified in many ways by Dr. Anthony Fauci, aided and abetted by advisors like his son-in-law, Jared Kushner, hijacked the president’s agenda. Now, the Trump administration has an unlikely yet monumental opportunity for health reform, which can start on January 20 with an investigation into Moderna’s cover-up.
The Covid response doomed Trump 1.0. Whether one regards this as a monumental error, the betrayal of a president by his advisors, an event beyond the president’s control, or a deeper and more complex plot involving everything and everyone associated with the government, both in the US and around the world, there is no question of the scale of the calamity for the public. The shots are part of that, the capstone failure of a long line of foreshadowing with lockdowns and all that was associated with pre-pharmaceutical interventions. The antidote came not as a cure but, for many, the disease itself.
There must be truth if not justice.
COVID-19
Calls for COVID-19 vaccine recall – FDA’s own study finds DNA contamination in Pfizer vaccines
From LifeSiteNews
By Dr. Michael Nevradakis for The Defender
“It is alarming that the public is made aware of this contamination in an obscure journal that features high school science research. One has to ask, ‘Where is the FDA now?’ and ‘Why hasn’t the public been alerted of this?’”
The peer-reviewed study in the Journal of High School Science was authored by three high school students and performed at an FDA lab under the supervision of FDA scientists. The findings prompted renewed calls for a moratorium on COVID-19 vaccines.
A peer-reviewed study performed at a U.S. Food and Drug Administration (FDA) laboratory by high school students has confirmed the presence of a high level of DNA contamination in Pfizer’s mRNA COVID-19 vaccine.
The study, published December 29, 2024, in the Journal of High School Science, was authored by three students at Centreville High School in Clifton, Virginia, and performed under the supervision of FDA scientists.
Maryanne Demasi, Ph.D., an investigative medical reporter, was the first to report on the study.
READ: British doctor has medical license revoked over warning of COVID shot dangers
The research, performed at the FDA’s White Oak Campus in Maryland, found that levels of residual DNA in the Pfizer COVID-19 vaccine were 6 to 470 times higher than regulatory safety limits. The students tested two lots of the vaccine, finding they contained “residual DNA to a level that exceeds 10 ng [nanograms] per dose.”
“The potential health risk posed by residual small DNA fragments is currently unknown,” the study stated. However, the authors also said that DNA contamination may result in insertional mutagenesis – or DNA mutations – that can cause cancer.
Speaking last month on “The Defender In-Depth,” Kevin McKernan, who first identified DNA contamination in the shots in 2023, said DNA in vaccines can pose health risks because the DNA “could integrate into the genome and cause disruption of the genome … or it could disrupt other genes that are related to cancer.”
The FDA did not respond to multiple requests for comment on the study.
COVID vaccines ‘must be immediately recalled’
The new findings challenge “years of dismissals by regulatory authorities, who had previously labelled concerns about excessive DNA contamination as baseless,” Demasi wrote on Substack.
The findings also align with earlier reports from independent laboratories in the U.S., Canada, Australia, Germany, and France, she said.
McKernan, founder of Medicinal Genomics, told The Defender that eight studies have found DNA over the limit. “Very few studies are surveying a large number of lots, so each study is additive,” he said.
Epidemiologist Nicolas Hulscher said that in “light of this evidence, the COVID-19 genetic injections must be immediately recalled, to protect the public from further harm.”
Nikolai Petrovsky, Ph.D., director of biotechnology company Vaxine Pty Ltd., told Demasi that the findings are a “smoking gun” and that the new study “clearly shows the FDA was aware of these data.”
Christof Plothe, D.O., a member of the World Council for Health steering committee, agreed. He said:
So far, the European, Australian, and American health regulatory boards have denied any risks from plasmid DNA contamination in the COVID-19 injections despite nine studies by internationally known research teams.
All teams concluded that this contamination poses an unacceptable risk to three-quarters of the world’s population.… Three teams so far have demonstrated the integration into human cells. To what extent this is happening to everybody who was injected needs to be investigated.
READ: Children who got COVID shots more likely to catch the virus than those who didn’t, study finds
McKernan said that the FDA has long ignored evidence of the dangers posed by mRNA COVID-19 vaccines.
“The criteria for pulling these shots was established long before DNA contamination was first discovered,” he said. “I would hope that evidence of highly variable manufacturing would be grounds for immediate class 1 recall from the FDA. They are currently distracted with performing class 1 recalls on non-lethal hairspray.”
A Class 1 recall involves “a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”
According to Demasi, “The FDA is expected to comment on the findings this week. However, the agency has yet to issue a public alert, recall the affected batches, or explain how vials exceeding safety standards were allowed to reach the market.”
Plothe noted that Demasi presented evidence of DNA contamination to the FDA in September 2024, asking if the agency had launched an investigation or requested further testing of the mRNA vaccines by their manufacturers.
“Nothing resulted from this request,” Plothe said. “As nine studies have proven this severe contamination and repeated requests to health regulatory boards have not led to any consequence, we must ask about the motive.”
Brian Hooker, Ph.D., chief scientific officer for Children’s Health Defense (CHD), noted the irony of high school students discovering what the FDA has seemingly missed in the four-plus years since the vaccines’ introduction.
“It is ironic that it takes student researchers at the FDA to do the work of the FDA regulators,” Hooker said. “It is alarming that the public is made aware of this contamination in an obscure journal that features high school science research. One has to ask, ‘Where is the FDA now?’ and ‘Why hasn’t the public been alerted of this?’”
Demasi said that the significance of the new study’s findings is that they came from research performed at an FDA facility.
“Now that DNA contamination of the mRNA vaccines has been verified in the laboratory of an official agency and published in a peer-reviewed journal, it becomes difficult to ignore,” Demasi wrote. “It also places vaccine manufacturers and regulators in a precarious position.”
This article was originally published by The Defender – Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
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