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Video: Gov. DeSantis Seeks to Hold COVID Vaccine Makers ‘Accountable for Misleading the Public About the Vaccine’s Safety


TheGatewayPundit.com

 

Governor Ron DeSantis (R-FL) just openly declared war on the pharmaceutical industry.

DeSantis recently announced that his office intends to hold vaccine manufacturers accountable for making misleading and false statements about the vaccines.

DeSantis made the remarks at a private Republican Party of Florida (RPOF) gathering held in the Florida Governor’s Mansion, according to American Greatness.

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How Many Studies Will it Take to Convince Your Vaxx-Loving Friends and Family the Jabs Cause Myocarditis?


Mercola.com

Another Study Confirms Myocarditis Post Jab

STORY AT-A-GLANCE

  • A study estimated the incidence of myocarditis after COVID-19 shots and compared it with expected rates in British Columbia; a significantly increased risk of myocarditis was found following COVID-19 jabs
  • While seven myocarditis cases would be expected within seven days, the study found 99 cases among those who’d received the shots
  • Within 21 days post-vaccination, 141 cases of myocarditis occurred. The expected rate was 20
  • This worked out to a myocarditis rate of 1.37 per 100,000 COVID-19 doses, compared with an expected rate of 0.39 per 100,000 people who did not get the shots
  • Rates of myocarditis after COVID-19 shots were highest among males, those aged 18 to 29 years, people who received a Moderna COVID-19 shot and people who received two doses
  • The rate of myocarditis among males aged 18 to 29 who received Moderna’s COVID-19 shot was 22.9 per 100,000

Yet another study has revealed people who receive a COVID-19 shot are at an increased risk of myocarditis, or inflammation of the heart muscle.1 With symptoms similar to a heart attack, including chest pain, shortness of breath, abnormal heartbeat and fatigue,2 myocarditis isn’t something that young, healthy adults typically experience.

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Secret CDC Report Reveals at Least 1.1 Million Americans Have ‘Died Suddenly’ Since the COVID Vaccine Roll-Out

& another Government Report proves the COVID Vaccines are to blame


ExposeNews.com

The Covid-19 injections were meant to reduce the sudden surge of deaths the USA recorded in 2020 due to the alleged Covid-19 pandemic. But unfortunately, the official figures prove that the opposite has happened.

Official reports quietly published by the United States Centers for Disease Control (CDC) confirm that over 6 million Americans have died ever since the U.S. Food & Drug Administration granted emergency use authorisation to a Covid-19 vaccine in December 2020; with 2021 being a record-breaking year for deaths.

This sadly means that at least 1.1 million Americans may have ‘died suddenly’ during this time frame because according to the CDC reports there have been 1,106,079 excess deaths compared to the 2015-2019 five-year average.

And with further official Government figures confirming that mortality rates per 100,000 are highest among the vaccinated population in every single age group, it would appear Covid-19 vaccination is almost entirely to blame.

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Moderna Vaccine Injures 6 People Within Hours of Super Vaxx Center Opening


County health officials pulled the batch of Moderna vaccines from distribution at the center, claiming it was "surprising" to see so many adverse reactions in such a short time.

Infowars.com

A new COVID-19 vaccine “super station” closed just hours after opening once six people were injured from the Moderna jab.

The vaccine super center in San Diego’s Petco Park began turning people away after six people experienced “allergic reactions” from Moderna’s mRNA injection.

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Video: Banking on a Shot in the Dark


 

Story at-a-glance

  • In recent months, two Pfizer officials have bragged about moving vaccine science forward at a speed that disallows proper scientific protocols from being followed, and the release of reformulated mRNA COVID boosters without testing is now the norm
  • In November 2022, recently retired head of vaccine R&D at Pfizer, Kathrin Jansen, said “we flew the aeroplane while we were still building it. We couldn’t wait for data, we had to do so much at risk.” Pfizer compressed its vaccine development timeline from 10 years to a mere nine months by simultaneously developing and testing the product in human trials
  • Pfizer and other COVID jab makers hid side effects by eliminating the control groups long before the studies were over
  • Vaccine makers are readying to release other mRNA shots, many of which are being fast-tracked and predicted to receive authorization in months rather than years. Moderna is working on a three-in-one shot for COVID, flu and RSV (respiratory syncytial virus), and they seem to expect releasing it before clinical trials are finished
  • Pfizer quoted and relied on data from Israel when it sought approval from the FDA, and as it turns out, the Israeli government hid information about side effects. It didn’t even implement its surveillance system until a year after the shots rolled out, and when the data were analyzed, researchers concluded there were causative links between certain side effects and the jabs

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Unvaccinated Blood Sees Demand Increase All Around the World


Ethan Huff
AmericaFirstReport.com

Is it safe to get a blood transfusion from a donor or donors who got “vaccinated” for the Wuhan coronavirus (Covid-19)? Many say no, which all around the world is generating increased demand for “clean” blood.

Now that we know jabbed blood is tainted blood, many are demanding “pure” or “safe” blood from sources that were never contaminated with messenger RNA (mRNA), spike proteins, and the many other contaminants found in covid vials.

“Bacteria, viruses, prions, and parasites can be transmitted by blood transfusions likewise people vaccinated with the mRNA vaccine have the SARS-CoV-2 spike protein … in their blood,” reports Great Game India.

“The spike protein (travels the entire body) caused by the COVID-19 vaccination last for months (potentially permanently in the body for those who frequently take booster shots).” (Related: Check out the movement for clean transfusions in the post-covid injection era.)

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CDC Knew COVID Vax Associated with Myocarditis but Left Off Post-Vax Survey


JustTheNews.com

The earliest demographics to get COVID-19 vaccines, such as healthcare workers, reported a surprisingly high rate of serious complications from them, according to data the CDC turned over under court order.

Among the 10 million-plus users of the agency's v-safe active monitoring smartphone app through July — 8.5 million of whom signed up between December 2020 and April 2021, before all adults were eligible for COVID vaccines — nearly 8% said they required medical care after receiving the vaccines. 

For patients ages 3 and older needing such care, nearly 3 in 4 couldn't rely on telehealth visits. They required urgent care (48%), emergency room (15%) or hospitalization (10%). For infants, who were authorized to receive the jabs this summer and are enrolled in v-safe through parents or guardians, hospitalizations were much lower (2%) but urgent care much higher (66%).

Another 12% of v-safe users reported they were unable to perform normal daily activities, and 13% said they missed work or school, meaning 1 in 3 had more than mild adverse reactions. 

Well over 10 million symptom reports were filed each month from January through April 2021, dropping to 5 million in May and hovering around 1 million for the next few months. The reports jumped above 2 million again in October following President Biden's vaccine mandates for roughly 100 million workers, and dropped to the low- to mid-hundred thousands from January through July 2022.

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Covid-19 Injections: Massive Regulatory and Manufacturing Fraud


By Tessa Lena
AmericaFirstReport.com

STORY AT-A-GLANCE

  • Alexandra Latypova is an ex-pharmaceutical industry and biotech executive with a lot of experience in the areas of drug safety and clinical trials
  • Early on, she discovered that, based on the number of reported deaths and adverse events per lot, there was unprecedented variability in the toxicity of the product
  • According to Alexandra, the mRNA shots do not conform to their label specifications, and “in practice, both ‘blank’ and ‘lethal’ vials and anything in between is produced”
  • Having analyzed massive amounts of publicly available data, as well as documents that became available as a result of FOIA requests and other sources, she has found strong evidence of manufacturing and regulatory fraud

I recently had the pleasure of interviewing Alexandra Latypova, an ex-pharmaceutical industry and biotech executive, who has been investigating and exposing manufacturing and regulatory fraud related to COVID injections.

We talked about the industry standards that were not adhered to during the clinical trials and the manufacturing of those injections, about the vial content quality testing procedures that had not been put in place, about the “hot batches” and their geographical distribution, about signs of fraud at every stage of testing and manufacturing the product, and about the general condition of living in a world run by a mob.

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Video: Died Suddenly


Why do we never believe them? For centuries, the global elite have broadcast their intentions to depopulate the world - even to the point of carving them into stone. And yet… we never seem to believe them.

The Stew Peters Network is proud to present DIED SUDDENLY, from the award winning filmmakers, Matthew Skow and Nicholas Stumphauzer.  They are the minds behind WATCH THE WATER and THESE LITTLE ONES, and now have a damning presentation on the truth about the greatest ongoing mass genocide in human history.

 

 

 
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FDA Documents Confirm Pfizer's 2021 mRNA Vaccine Lots Had Different Formulations Based on Lot#


FDA documents confirm different Pfizer EUA mRNA formulations were injected into over a hundred million Americans. US government patent shows many more mRNA bioweapon formulations

When the emergency use (EUA) COVID-19 mRNA vaccines were first rolled out in the United States, many Americans questioned if different formulations were being distributed. Why? Because some people became severely injured or died after vaccination, while others seemed completely fine. Furthermore, some vaccine lots had higher incidences of severe injuries and deaths, while other lots and little to no adverse events per the VAERS database.

In a court of law, it would be difficult to argue that the incidence of adverse events by lot number is evidence that the EUA mRNA vaccines varied in formulation. One could simply counter argue that people respond differently to biologics and drugs. The varying rates of adverse events can easily be dismissed as a coincidence or potentially attributed to some other factor affecting residents in that region, such as higher rates of obesity.

What one can’t argue against is Pfizer’s and the FDA’s (CBER) own admission that Pfizer’s EUA mRNA vaccines vary in formulations.

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Who's Online
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Please Support Us With A Purchase