Heart failure within three years predicted. Right-side heart failure.
Damage is cumulative with every shot.
d-dimer test by the way
and there’s this
Zombie theory, for a little Apocalypse style fun.
The Lame Cherry will remind readers who are Biblical ignorant that People are warned to fear God Who can destroy both body and soul in hell. Souls are immortal. They can be destroyed. We do not know for certain if the Elon Musk charge will be necessary to sustain this synthetic immortal. In other words are the vaxed humans evolved like lightbulbs in needing electricity to light up. If that is the case, then this SatNet grid with 6G would need to be in continuous operation or the vaxed would begin degrading. We do not know of these transformed biological units can self generate. It is one thing to be Jesus in Pure Life and another for some grubber like you who is chemical electric sustained, needing oxygen, minerals and amino acids to create a body life current for the host soul to be housed in.
This mRNA is not changing the soul as the soul is not organic. So the body is what is being changed to an immortal status. As the Lake of Fire will short out or consume the soul, the reality is if the 1% gets this wrong, there are going to be perpetual rotting people who will not die. The subject which has not been stressed is, what if this vax welds the soul to a synthetic body which will not die. But will rot. Imagine being locked in a body in a permanent link to the soul, and being in perpetual pain, or a torment like hell.
Like a binding spell. Spooky.
Prions are transmissible, pathogenic agents that are able to induce abnormal folding of specific normal cellular proteins in the brain. Prion protein damage causes tiny holes to form in brain tissue, making it appear sponge-like under a microscope. It is usually rapid and always fatal. (source)
Frighteningly. the spike protein outer shell of the coronavirus contains “prion-like regions” that give the virus very high adhesion to ACE2 receptors in the human body. The study published by the Human Microbiology Institute lays it out:
“In this study, using the PLAAC algorithm, we identified the presence of prion-like domains in the SARS-CoV-2 spike protein… SARS-CoV-2 demonstrates a 10- to 20-fold higher affinity for ACE2.”
Currently, the world is struggling with the coronavirus disease 2019 (COVID-19) pandemic, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Prion-like domains are critical for virulence and the development of therapeutic targets; however, the prion-like domains in the SARS-CoV-2 proteome have not been analyzed. In this in silico study, using the PLAAC algorithm, we identified the presence of prion-like domains in the SARS-CoV-2 spike protein. Compared with other viruses, a striking difference was observed in the distribution of prion-like domains in the spike protein, since SARS-CoV-2 was the only coronavirus with a prion–like domain found in the receptor-binding domain of the S1 region of the spike protein. The presence and unique distribution of prion-like domains in the SARS-CoV-2 receptor-binding domains of the spike protein is particularly interesting, since although the SARS-CoV-2 and SARS-CoV S proteins share the same host cell receptor, angiotensin-converting enzyme 2 (ACE2), SARS-CoV-2 demonstrates a 10- to 20-fold higher affinity for ACE2. Finally, we identified prion-like domains in the α1 helix of the ACE2 receptor that interact with the viral receptor-binding domain of SARS-CoV-2. Taken together, the present findings indicate that the identified PrDs in the SARS-CoV-2 receptor-binding domain (RBD) and ACE2 region that interact with RBD have important functional roles in viral adhesion and entry.