by Suzanne Hamner, DC DirtyLaundry:
Several prominent physicians, doctors, Sons of Liberty Media Health and Wellness expert Kate Shemirani, her colleague Dr. Kevin Corbett, and I have postulated that the current experimental mRNA injection for coronavirus, aka COVID-19, could alter one’s genetic code or DNA. Bill Gates stated it, which was included in my video “Human Genome 8 and mRNA Vaccine” on Brighteon.com. It is one reason the term “experimental human genome altering mRNA injection” has been used to describe the jab being foisted onto the mostly unsuspecting public. While many in the media, Dr. Anthony Fauci and his merry band of chronic liars, and “fact checkers” have declared this claim as false, a video of a TEDx Beacon Street talk by Tal Zaks, chief medical officer of Moderna, Inc., one pharmaceutical company manufacturer of the experimental mRNA technology injection, confirms mRNA injection for COVID-19 can change your genetic code or DNA. This TEDx Beacon Street talk occurred in 2017. H/T to YouTube channel Silview Media Backup Channel.
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Zaks calls it “hacking the software of life”. In the first minute of the video Zaks states, “we’ve been living this phenomenal digital scientific revolution, and I’m here today to tell you, that we are actually hacking the software of life, and that it’s changing the way we think about prevention and treatment of disease.” [Emphasis mine.] He even repeats that they (Moderna) think of it like an operating system, which the Moderna website indicates as “Our Operating System”.
At one minute in, Zaks states, “In every cell there’s this thing called messenger RNA or mRNA for short, that transmits the critical information from the DNA in our genes to the protein, which is really the stuff we’re all made out of. This is the critical information that determines what the cell will do. So we think about it as an operating system. …. So if you could actually change that, … if you could introduce a line of code, or change a line of code, it turns out, that has profound implications for everything, from the flu to cancer.” [Emphasis mine.]
When “changing” a line of code or “introducing” a line of code” (referring to DNA), the “code” or DNA is then altered, meaning the individual or “subject” has now had their genome changed to what the “scientists” have coded. The individual or subject is no longer a creation of God but a creation of man, meaning the individual or subject could be the object of a “patent”. He goes on to say, the mRNA would tell the cells to “code” for the protein of the “virus”. This “viral protein” is foreign to the body. The individual’s body is making a foreign protein the immune system is to attack. When the body makes a protein the immune system then attacks, your immune system is attacking a protein your body is making, meaning what is occurring in an “auto-immune response” or “auto-immune disease”.
This has been repeated a number of times by experts, physicians, nurses and countless others. As readers can see, none of us were “whistling Dixie”. Zaks talks about turning this system on; however, there is no way to turn it off. When do the cells know to stop making this “viral protein”? The cells don’t; therefore, this continues for the duration.
In a normal vaccine, the immune system attacks the limited amount of “particles” in the adjuvant to produce antibodies or immune response that the body can recognize at a later time if the individual comes in contact with the same or similar “particle”.
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The study Zaks cites at the 3:12 minute mark can be found and read here. The abstract is contained on the NIH Pub Med Library website. In the full test of the study on ResearchGate, the mention of “Luciferase” occurs on page 10. A crucial piece of information in this study is contained on page 4 – “Ferrets immunized with 200 micrograms and challenged [exposed to influenza H7N9 via IN (intranasal)] on day 49 had viral loads below the level of detection”. If a viral load was “below the level of detection”, two questions emerge: 1) did the ferrets even contract H7N9 through intranasal challenge; and, 2) if a viral load is below the level of detection, how do you know the animals even had a viral load? This would bring into question the efficacy of the injection.
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