How the CDC Lied about Shot Injury

The month was January 2021, only a few weeks into the mass rollout of the injection called a vaccine. The Centers for Disease Control and Prevention had outsourced its collection of data from the VAERS system – designed to monitor vaccine safety – to General Dynamics Information Technology. GDIT wrote the CDC a memo dated January 15.

“The number of incoming COVID-19 reports has significantly exceeded the estimated maximum of 1,000 reports per day,” the memo to the CDC said. “As a result, GDIT is unable to meet processing and other timeframes (data processing, telephone inquiries, clinical inquiries, etc.). GDIT has reache [sic.] out to the Pogram [sic.] office and OAS for guidance and support.”

Indeed, the floods of reports were many times the “worst-case scenario” that General Dynamics had anticipated, so it admitted that it could no longer process them.

The five-alarm fire should have been obvious. At that very instant, if not long before, the shots should have been pulled. Banned immediately for all groups. Apologies should have been offered. Industry executives should have been put on trial because later document releases proved that they knew the dangers. Victims should have been compensated from industry profits, with payouts in the many tens of billions.

After all, this is how dangerous pharmaceutical products had been treated in the past, after only a few reports. But in this case, it was different. Everything that had happened since March 2020 had led to this moment; all the closures, the stay-at-home orders, the smashed small businesses, the supply-chain breakages, the multiple trillions in spending and money creation, the capacity restrictions, and the censorship.

Without an effective and safe shot, all of this would have been a waste. There would have been civilization-wide fury. Neither the politicians, nor bureaucrats, nor media, nor industry, could risk that.

Plus by law, the companies that made the shots and the institutions that started forcing them on people bore no liability for harms. This was due to the special status called Emergency Use Authorization, enabled by the PREP Act, that even bypassed normal testing standards at the FDA.

The agency receiving this alarming communication was the CDC. The CDC has a newsletter. It’s called the Morbidity and Mortality Weekly Report.

On February 19, 2021, now two months into the shot release, and hundreds of thousands of VAERS reports pouring in, so many that they could not process them, the MMWR released its first report on the shot

The primary author was Julianne M. Gee, an epidemiologist in the CDC’s Immunization Safety Office, part of the National Center for Emerging and Zoonotic Infectious Disease). She still works there today. The senior author is Tom Shimabukuro, currently deputy director of the Influenza Division in the National Center for Immunization and Respiratory Diseases.

In this report, they wrote a conclusion from having examined 6,994 reports: “Monitoring, conducted as part of the U.S. vaccination program, indicates reassuring safety profiles for COVID-19 vaccines.”

The trouble is that at that point, there were already 107,000 reports, so her report only examined 6 percent of the total on that date. General Dynamics had already told the CDC that they could not process beyond their “worst-case scenario” of 1,000 reports per day. VAERS analyses depend on reports being processed—coded, reviewed for seriousness, and made available for statistical screening and clinical follow-up. When intake substantially exceeds processing capacity, the analyzed dataset lags the raw reports.

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I followed Vaers from day one ( up until they pulled the reports at 900,000 something) and was ridiculed for not taking the mRNA kill shot at work. Stood my ground, was granted my exemption two months later.

The dead I know that died from the jab is over a dozen, the on going debilitating effects of those spike proteins is on going. There are treatments to get that mRNA out of your body, if you took the jabs pursue the treatments.

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