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Horowitz: Study of young boys after vax shows cataclysmic prevalence of heart problems, blows open sudden death theory

What will it take for Republicans to stand united and call for the end of these shots, the investigation of their creation and distribution, and compensation for those injured? Do they really fear the vacuous pejorative of “anti-vaxxer” more than they love a generation of children?

In January, CDC researchers conceded in JAMA that the over 50,000 reported cases of myocarditis and pericarditis in VAERS are “likely” underreported. If they are willing to concede that point, it should be abundantly clear to thinking people that the number of diagnosed cases of myocarditis, and certainly those reported to VAERS, were likely the tip of the iceberg due to the prevalence of subclinical myocarditis. A new preprint study from Thai researchers confirms those suspicions in spectacular fashion with sickening ramifications.

The researchers conducted in-depth cardio health surveillance of 301 adolescent children (13-18 years old), 202 of whom were boys, before they got jabbed and followed them for up to 14 days after the second dose of Pfizer. The findings were mind-blowing. Seven of the 202 boys (3.5%) developed clinical or subclinical myocarditis/ pericarditis! This is not 1 in 5,000 or 1 in 10,000 as we were led to believe, which was bad enough. This equals 1 in 28 of all teenage boys jabbed! Oh, and remember, Moderna has been proven to be even worse for heart inflammation, likely because it is three times the dose of Pfizer.

Keep in mind that these numbers are just for 13- to 18-year-olds, but males around that age and a little older are also in the target zone for myocarditis. There are roughly 21 million boys ages 10-19. There are another 11 million ages 20-24. This means that if the bad guys got their way, there’d be roughly 1.1 million boys and young men with myocarditis of some sort! And we know the risk exists for other ages and for women, just at a lower rate.

Even for the clinical myocarditis, three developed pericarditis or myocarditis and two were hospitalized. That is a cataclysmic level of heart damage, which, if proven true, would certainly explain the anomalous excess cardiac deaths, sudden deaths among young people, and increase in EMS emergency home calls.

More broadly, 18% had abnormal ECGs, and “cardiovascular effects were found in 29.24% of patients, ranging from tachycardia, palpitation, and myopericarditis.”

Now, this doesn’t definitely prove that such a whopping percentage of people incurred heart damage from the shot just based on these markers, but it does demonstrate that subclinical myocarditis affecting an enormous number of people is a real concern at this point. It would also make sense why it appears that elite athletes suffered more severely early on because their level of exertion will bring out that latent heart inflammation much more suddenly than someone with a more sedentary lifestyle.

Before anyone dismisses this as a random preprint, the numbers harmonize perfectly with concerns expressed by the FDA BEFORE it authorized the Comirnaty shot. According the Pfizer informed consent document (p. 5), the company recognized the risk of myocarditis can be as high as 1 in 1,000. But the FDA was concerned that subclinical myocarditis might be even more of a problem.

In the Pharmacovigilance Plan Review Addendum for Comirnaty, the FDA conceded (p. 3-4), “Incidence of subclinical myocarditis and potential long-term sequelae following COMIRNATY are unknown.” However, they did note that a previous study on a smallpox vaccine “suggested an incidence of possible subclinical myocarditis (based on cardiac troponin T elevations) 60-times higher than the incidence rate of overt clinical myocarditis.”

Sixty times greater! If you do the math, that equals 1 in 17 individuals for the highest-risk group, aka young men and teenage boys. They asked Pfizer to complete a study on subclinical myocarditis, but it won’t be completed for another year, long after they pressured and sometimes mandated any teenage boy to get the shot if he wants to join the military, go to college or medical school, or compete in sports. There are still schools in America requiring children to get this dangerous shot. Meanwhile, Denmark won’t even make the shots available for children any more.

Consider that there are 51,000 cases of myocarditis or pericarditis reported to VAERS, which we already know is woefully underreported even for clinical-level illness. If subclinical myocarditis is 60 times greater, that would encompass more than 3 million people.

How has the government allowed this to be approved, much less mandated and continued long after the safety signals were glaring and blaring, without conducting cardiac MRIs on these boys on autopsies on those who die suddenly? One of the ways our government is violating the Nuremberg Code is by not warning people to check for subclinical myocarditis before it’s too late. That requires a cardiac MRI, which is very expensive and won’t be covered by insurance. Rather than funding the latest escapade in Ukraine, our government has an obligation to fund cardiac MRIs for those who got the shots, especially those most at risk for myocarditis. Why are government officials scared to randomly sample the first 5,000 people they find to undergo a cardiac MRI? They sure don’t lack the funds.

Dr. Kirk Milhoan, a pediatric cardiologist and former flight surgeon in the Air Force, tells CR that the heart issues were obvious from early on, given the toxicity of the spike protein, which is why this should never have been given to an entire population, even if it had efficacy against the virus. “We give known cardio-toxins for those with difficult-to-treat cancers that are not amenable to less toxic chemotherapeutic agents. We should never give such an agent to healthy children and adults, whose risk of hospitalization and death is much less than 1%.”

Milhoan cites a new study touted by the American Heart Association demonstrating that the spike protein is cardio-toxic. “This has been clear clinically, and now the cellular mechanism has been identified. No one should be given a cardio-toxic therapeutic for the SarsCov-2 infection. Even more, we should not be asking the body to be making the cardio-toxic protein via DNA or mRNA injectable products.”

The public has been convinced to credulously believe a dastardly lie that somehow there is a substantial risk of myocarditis from natural infection, even more so than from the vaccine. Let’s put aside the fact that these shots do not work to stop such infection anyway. The data simply does not bear this out. A Danish study of 74,611 children found 0 diagnosed with myocarditis in the two months following a COVID infection, compared to a 1/2,700 rate in adolescent boys following two doses of Pfizer. Now, obviously, this study only measured diagnosed cases, not nearly as thorough a physical workup as conducted by the smaller Thai study, but it clearly shows that in an apples-to-apples comparison, the risk for myocarditis from the shots is exponentially higher than the risk from the virus.

In fact, it’s not clear altogether that there is a risk of myocarditis from the virus above the background rate at all for those who don’t suffer critical illness, which is nearly every teenager. A recent Israeli retrospective cohort study of 197,000 patients within the Israeli Clalit Health Services Organization concluded based on the incidence of myocarditis and pericarditis in the system from March 2020 to January 2021 (pre-vaccine COVID era) that the incidence of myocarditis and pericarditis in COVID-infected patients was not increased relative to uninfected, matched controls.

“There is not yet definitive EMB/autopsy proof that SARS-CoV-2 causes direct cardiomyocyte damage in association with histological myocarditis,” wrote the Israeli researchers in the Journal of Clinical Medicine. “Post COVID-19 infection was not associated with either myocarditis (aHR 1.08; 95% CI 0.45 to 2.56) or pericarditis (aHR 0.53; 95% CI 0.25 to 1.13). We did not observe an increased incidence of neither pericarditis nor myocarditis in adult patients recovering from COVID-19 infection.”

How is it that to this day, Florida Governor Ron DeSantis is the only one raising concerns about these shots and Ron Johnson is the only senator in D.C.? We are long past the point where not only should these shots be destroyed, those who knowingly promoted them despite their dangers and continue to do so despite glaring safety concerns should face a Nuremberg-style reckoning.
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Horowitz: The man who holds the key to bringing down the Pfizer pfraud

On today’s special show, we are joined by Augusto Roux, a criminal law attorney from Buenos Aires who participated in the largest Pfizer clinical trial site. He shares his riveting story of how he was immediately injured after the second dose and suffers from pericarditis and liver damage. Instead of recording his injury in the clinical trial data, the company blamed it on COVID (even though he tested negative) and diagnosed him with anxiety. He shows how Pfizer committed fraud and violations of human rights every step of the way. He also discovered how the company covered up two deaths at the same trial site and how hospital officials told him they treated numerous people with severe injuries in the trial. None of them were recorded. We need a Nuremberg trial, and Augusto might have the evidence to conduct it!

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Horowitz: Why there is an urgent need to study effects of COVID shots on reproductive health

When a private actor seeks to get a product approved for human use, the company must prove conclusively using the scientific method that the product is safe. How much more that principle applies when governments endorse, market, and mandate the use of the product. Yet here we are, 16 months into the release of this product, with endless safety signals showing a diverse array of injuries from the shot, but we are the ones being forced to conclusively prove that it causes each one of these maladies to the Nth degree. Meanwhile, the shots are still mandated in the military, for health care workers, and for many others.

Nowhere is the principle of “unsafe until proven safe” applied more rigorously in the world of pharmaceuticals than products marketed to pregnant women and young children. Yet the shots and other COVID therapeutics were approved for pregnant women and children without running proper short-term, much less long-term, safety studies, regardless of the health status or risk factors of those people, including those who already had COVID.

In the FDA’s “Summary Basis for Regulatory Action on Comirnaty” – published nearly a year after the shot had already been administered and, in some cases, mandated upon pregnant women – the drug regulator stated plainly that proper information for use for pregnant and nursing women is missing. "Missing information: Use in pregnancy and lactation; Vaccine effectiveness; Use in pediatric individuals <12 years of age," the FDA divulged.

Incidentally, this disclosure is right next to the admission that Pfizer knew about both the risks of heart inflammation and vaccine-associated enhanced respiratory disease, the latter of which might be the culprit for recent trends of negative efficacy, with the vaccinated appearing to get sicker from the virus.

It should also be noted that in Comirnaty’s (Pfizer BNT162b2) purple cap package insert, the label states unambiguously that “available data on Comirnaty administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy.”

Then, of course, there is Pfizer’s informed consent document (p. 10), which states, "The effects of the COVID-19 vaccine on sperm, a pregnancy, a fetus, or a nursing child are not known."

That right there demonstrates that the pressuring and even mandating of the shot on pregnant women violates the Nuremberg Code, and anyone who claims that the vaccine has been affirmatively proven safe in pregnant women is publishing false information.

It is in that vein that I present the latest report on stillbirths and infant deaths in Iceland by local daily paper daily Frettin, based on new data from Statistics Iceland. Given that Iceland is a small nation of just 366,000, it is easy to pick up on sudden shifts in health outcomes, which makes the fact that there has been a precipitous rise in stillbirths in 2021 all the more alarming. In 2021, there were 17 stillbirths and 35 first-year infant deaths reported in Iceland, up from just 9 and 19 respectively in 2020. In other words, stillbirths and first-year infant deaths nearly doubled.

According to Frettin, when you factor in the number of births every year, the average stillbirth per 1,000 live children for the last nine years (2011-2020) is 2 per 1,000. The increase for 2021 over the previous nine-year average was 75%. The increase in perinatal mortality (includes both stillbirths and children who die within the first week) is 82% in 2021 compared to the average of the previous nine years before that. The number of deaths in infants for the entire first year increased by 100% compared to the average of the previous nine years.

We don’t know the cause of the increase, but we do know there was no increase in 2020 when we only had COVID has a novel public health crisis but did not yet have the shots on the market. We don’t know if the shots had anything to do with this increase, but we do know the shots have caused a ubiquitous disruption in menstrual cycles, we do know that the lipid nanoparticles are deposited liberally in the ovaries, and we do know that the lipid nanoparticles are hyper-inflammatory. Again, why should we have to wait years to study these safety concerns to take the shots off the market until they are proven unsafe, rather than removing them from the market until they are proven safe?

There are other concerning data points from two hospitals in Israel revealed by Josh Guetzkow via an Israeli FOIA request. In May 2021, Rambam hospital in Haifa, Israel, had 42 SBMAs (stillbirth, miscarriage and abortion), which was nearly double the average of the May total from the previous two years and 30% higher than the highest number of any month in the previous two years. Moreover, the rate among vaccinated women in that hospital was 34% higher than among the unvaccinated. Also, Sheba Medical Center, Israel’s largest hospital, experienced the highest SBMA count in June, right around the time of the vaccine take-up for pregnant women. There were 146 SBMAs that month, 30% higher than the average of the previous two years and 11% higher than the largest number of SBMAs for any month in the previous two years, which was 132 in March 2019.

To this day, not a single government has attempted to follow up on these safety signals and determine what is indeed causing these increases. We already know from Pfizer’s released documents that the company knew of thousands of maladies and injuries reported after the first few months of its vaccine campaign. Moreover, a confidential Pfizer document (p. 29) recently revealed that the company has not and will not conduct genotoxicity and carcinogenicity tests, which are standard for vaccine products.

Thus, they have no desire to find out whether the shots can cause mutations in DNA or cancers. Remember, one study from Sweden has already found “the spike protein localizes in the nucleus and inhibits DNA damage repair by impeding key DNA repair protein BRCA1 and 53BP1 recruitment to the damage site.” That doesn’t exactly sound like a product I’d want to give to those who want to have children until we have better studies.According to the Declaration of Helsinki on medical ethics, “Physicians may not be involved in a research study involving human subjects unless they are confident that the risks have been adequately assessed and can be satisfactorily managed.” This is not just any research study but one involving 2 billion human beings, with hundreds of thousands of pregnant women being used as lab rats before adequately assessing risks and after some risks are already apparent. It’s a new bio-medical paradigm of “mandate first, study never.”

Horowitz: Who will be the first governor to block the Pfizer injection for babies?



The perception in the body politic is that the Democrats want an off-ramp from COVID and that many people have realized the existing failures were a catastrophic mistake. However, just as we were confronted with some of the worst battles seemingly at the end of WWII – the Bulge and Okinawa, for example – we are now facing the most immoral and unscientific COVID measure of all. Originally, the FDA planned to approve the now expired vaccines for infants, toddlers, and babies yet to be born. They have since delayed the authorization, but that just gives us a few weeks to put the nail in the coffin of this immoral experiment.

Our babies are now lab rats. After Fauci himself has admitted the emergency part of the pandemic is over, they plan to use an emergency authorization to approve the shot for a population for which there never was an emergency. But facts, laws, and morality no longer matter when Pfi$er comes for its fair share. And evidently, $54 billion in revenue is not enough.

Originally, Pfizer planned to submit its EUA application for kids 6 months to 4 years old to the FDA’s Vaccines and Related Biological Products Advisory Committee on Tuesday. On Friday, the company announced it would wait until the trial on three doses for children is finished, rather than going ahead with the two-dose application, which failed to show any improved immunity. However, the company still plans a three-dose submission for some time in April.

Pfizer’s own trial thus far found no benefit for those children, and even the most conservative estimate of adverse events renders this endeavor all risk and no return. And of course, there is no trial on the current variant. Yet our government was already distributing the vials. We call that a violation of the Nuremberg Code.

What could possibly be the motivation to pursue this authorization so quickly when the emergency has passed and the virus circulating seems to have a greater affinity for vaccine-mediated antibodies? Israel, with the most boosters in the world, is experiencing its worst death curve precisely now, even with the mildest variant. In some U.K. age groups, the triple-vaxxed have over a 2.7-fold greater case rate than the unvaxxed.

Meanwhile, Pfizer is trying to find data showing three doses do “something” for children, when we already know from the past 12 months with adults that even if they offer some antibodies, they wane and run the risk of causing enhancement and negative efficacy. Yet Pfizer will cleverly just show two or so months of the trial before the waning kicks in, just as with the adult trials.

Is there not one righteous man left in Sodom who has any degree of curiosity as to why this is happening? It’s one thing for older people to use this experiment with informed consent during the height of the pandemic. One could conceivably say they will turn a blind eye to all adverse events because of the perceived short-term benefit. But nobody can articulate any benefit for this group of kids at this time for this variant with these shots, and we sure have a lot of known and unknown safety signals about short-term and long-term consequences. This was so rushed that they even merged three phases all into one phase.

There’s only one plausible explanation for this maniacal alacrity to shoot up the babies, and it can’t just be about money alone. They want to destroy the one remaining demographic control group in this country that remains untarnished by this great human experiment. As we begin to witness the reproductive, cardiovascular, neurological, and immune system damage, the media and the medical system will seek to blame the death and destruction on everything but the shots. In order to succeed, they cannot allow a single age group to evade the reach of the great experiment.

Last week, the European Medicines Agency announced it will investigate reports of "heavy menstrual bleeding and absence of menstruation" after mRNA COVID shots. We have known about these safety signals from day one, yet the global health entities chose to ignore them until after all of the young women and even children got the shots. How could someone in good conscience allow this shot to now enter the arms of babies and toddlers before this safety signal is fully investigated?

Now imagine if the federal government began distributing Planned Parenthood abortion centers throughout all the red states. Do you think the governors would sit idly and say, “Well, at least there is no mandate to get an abortion, it’s simply optional”? Hell no! They would ban that distribution throughout the state. Well, this is an even bigger pro-life issue, because it will affect exponentially more children. It’s no longer enough for governors to remain neutral on the shots. They must pledge to ban them in the states, and that begins with babies and toddlers. Pro-life means so much more than just fighting abortion.