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Dr. Kevin McKernan, a microbiologist, has made a startling discovery regarding the Pfizer and Moderna vaccines. He has found “unacceptable levels” of double-stranded DNA plasmids in these vaccines. In an interview with “The Freedom Corner with Peter Sweden,” Sasha Latypova, an executive in pharmaceutical and medical device research and development, elaborated on McKernan’s findings.

Latypova emphasized that the presence of DNA contamination is a significant issue. These replicable DNA plasmids have the ability to invade both human cells and bacteria in the gut. This invasion can lead to the replication of antibiotic-resistant genes, sepsis, cancer, and other health problems.

The World Council for Health (WCH), composed of experts, has also confirmed the global risk of DNA contamination in mRNA vaccines. They find the existence of replicable DNA plasmids in both monovalent and bivalent vaccines to be unacceptable. Consequently, they have called for an immediate cessation of the COVID-19 vaccine program.

In addition to DNA contamination, Dr. McKernan has uncovered the presence of Simian virus (SV40) promoters in Pfizer’s mRNA vaccine. It is important to note that the SV40 detected in the vaccine is only a viral fragment and not the complete virus. Nevertheless, this discovery still poses a potential risk of promoting cancer.

Originally discovered in rhesus monkey kidney cells used for producing inactivated polio vaccine (IPV) and oral polio vaccine (OPV), SV40 was identified as an animal carcinogen. In response, a law was enacted in 1961 to prohibit its presence in vaccines. (For more information on SV40 and its connection to cancer-causing viruses concealed in polio vaccines, refer to “The true story of SV40, the cancer-causing virus hidden in polio vaccines.”)

On Friday, May 19, the U.S. Department of Agriculture (USDA) announced the detection of an atypical case of bovine spongiform encephalopathy (BSE), commonly known as mad cow disease, in South Carolina (SC). This marks the seventh instance of BSE detection in the United States since 2003.

The USDA stated that the affected animal did not enter the slaughter channels and posed no risk to the food supply or human health in the country. Given the United States’ negligible risk status for BSE, the agency does not anticipate any trade impacts resulting from this finding.

According to Clemson University, a leading public research institution in SC, the cow originated from Tennessee and tested positive for atypical BSE.

Upon arrival at the SC plant, the cow displayed symptoms of the disease and was euthanized. Samples were sent to a lab in the National Animal Health Laboratory Network (NAHLN) for testing, which initially raised suspicions of BSE. Subsequently, the samples were sent to the USDA Animal and Plant Health Inspection Service’s (APHIS) National Veterinary Services Laboratories (NVSL), where they confirmed the presence of atypical L-type BSE.

Atypical BSE primarily occurs in older cattle and appears to arise rarely and spontaneously in all cattle populations.

Dr. Michael Neault, South Carolina state veterinarian and director of the university’s Livestock Poultry Health Department, referred to this case as an “isolated incident.”

Among the six previous cases in the country, the first was a classical BSE case in a cow imported from Canada two decades ago, while the rest were atypical (H- or L-type) BSE cases.

APHIS emphasized that the United States has established a longstanding system of interlocking safeguards against BSE to protect public and animal health. The most crucial measure involves the removal of specified risk materials, which are parts of an animal that may contain BSE if the animal is affected.

Another significant safeguard is a robust feed ban that prevents the transmission of BSE to cattle. Additionally, the ongoing BSE surveillance program enables the USDA to detect the disease even at very low levels within the U.S. cattle population, as evident in this recent detection.
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