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Dr. Mike Yeadon Dec. 4, 2023

The body is trained exquisitely to detect and attack non self foreign things. If you inject a person with a gene that encodes a foreign piece of protein, like a spike protein from a foreign organism, your body will detect that. And every single cell that takes up that material and expresses foreign protein will be attacked and killed by your immune system. You’re making a specific material called spike protein. Those materials are biologically active. That is, if you add them to human blood, for example, they start to coagulate, it clots. 


 So now you’ve got a genetic sequence that forms foreign proteins. That means your body attacks and kills every cell that does it. And if you should release any of that protein in your blood, it will form blood clots. If it releases it near nerves you will get one or other of several neurological defects. These are formulated in fatty globules called lipid nanoparticles. What they do is disguise the foreign genetic information so your body doesn’t see it initially until it gets inside your cells and it goes all around your body. 


It will glide through the cell wall as if it wasn’t there. And that was the entire point of it. So that means these materials don’t just go to your lymph nodes. They go into your brain and your blood and every organ in your body. So, by design, these agents cause an autoimmune attack on every tissue. They make your body form a well understood biological toxin that can damage multiple organs in your body.





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           By Dr. Ah Kahn Syed Dec. 5th, 2023

Covid injections contain therapeutic levels of DNA – this is the definition of gene therapy. In addition to the declared mRNA, plasmid DNA has now been found in the mRNA injections. DNA lasts forever and if it integrates into your genome, you will produce its product forever. Plasmid DNA is the lab-based circular DNA particles that is replicated and then used to create the mRNA that goes into your “short-lived” vaccine. 



Dr. Phillip Buckhaults has to say about the Buckshot {vaccine] in his speech to the South Carolina Senate hearing: It’s because in this one product there are at least 5 ways in which the product design and manufacture ended up with mechanisms that increase the risk of DNA going into the nucleus of your cells, thus modifying your genome. The LNP is a transfectant medium. The lipid acts as something that takes the nucleic acid product (DNA or RNA) into the cell and potentially onto the nucleus. That’s what transfection agents do. In other words, those lipid nanoparticles are designed to get DNA into the nucleus of cells. 



So, what on earth is that I hear you say? Let’s break it down: Linearised – Plasmid – DNA. Well DNA is what shouldn’t be in the product. It’s the nucleic acid type that makes up your genome, the stuff that is the blueprint for you. RNA is derived from DNA and makes the proteins that enable you to live. The bottom line being that, in general, if you want to have an effect on an organism (e.g., a person) using genetic methods, you can do this temporarily with RNA – which will then produce protein and should then degrade so it doesn’t produce any more. But if you want to make it more permanent you would use DNA and integrate it into the genome. 



Then when called on it will produce RNA which will produce protein. That process could happen for ever under the right circumstances.The step for RNA to produce protein usually happens immediately when RNA is produced (or introduced) in the cell. But for DNA to enact this process (to induce transcription and then translation) requires the DNA to have a signal to act. This is usually from a promoter which can respond to local signals and start the transcription process (it needs to be regulated so that it is not switched on all the time). The point is that, if foreign DNA gets into your genome all hell can break loose. 



Linearised Plasmid is the circular loop of DNA that is used to transfect the bacteria E.Coli. This form of DNA is very good at getting into bacteria and getting them to produce what you need. Plasmid DNA is not normally that dangerous to humans because it is readily destroyed by circulating enzymes. The problem comes when the plasmid DNA is encapsulated in a lipid nanoparticle. Then it doesn’t get destroyed and whichever organism it gets injected into may react in a similar way to the #poojabs bacteria it was intended for. So, having lab-plasmid DNA intended for bacteria contaminating your “RNA therapy”, fragments? 



The 72bp sequence from that SV40 enhancer region was required in order to transport plasmid DNA (or any introduced DNA, for that matter) into the nucleus of cells (other than those undergoing cell division). That sequence was coincidentally the only one that could have been chosen that had a specific property of facilitating the transport of any foreign DNA that happened to be present into the nucleus. Essentially, the spike protein (not the RNA or DNA) contains a special peptide sequence which acts as a nuclear transporter of any DNA that is attached to it. It’s one of many mechanisms for nuclear transport (that is, carriage of DNA into the nucleus).




The common theme is that the DNA needs a nuclear localisation helper, which can be a Nuclear Localisation Signal (NLS, a specific sequence of amino acids in a protein in the cell) or a DNA transport sequence (DTS, discussed above in the SV40 section).  The furin cleavage site, that was touted as the scary insertion that caused virulence of the scary virus – was kept in the vaccine sequence.The retention of the “furin cleavage site” part of the spike protein – which is highly inflammatory and should not have been kept in the design of a vaccine –



 rendered an additional method by which any fragments of DNA that were present could be transported to the nucleus and integrated into the genome.I’ve come to the end of this little trip around the “mRNA” covid injection sequences and their intentional absolutely coincidental properties that make transfer of their plasmid DNA into the genome highly likely. And of course, this is dose dependent so the more doses you have the more likely the plasmid fragments will be to integrate into your genomic DNA.