The science has spoken, vaccines activate the ancient retroviruses that pretty much turn you into a prehuman vegetable.
HERV-W is not the only retroviral game in town. Researchers recently discovered that a retrovirus-like protein known as PEG10 directly binds to and secretes its own mRNA in extracellular virus-like capsids. This behavior is eerily similar to that of the ARC1 retroviral protein now understood to be critical in the formation of memory at synaptic sites. Incredibly, researchers are already well on their way to pseudotyping these virus-like particles with fusogens to create an endogenous vector for delivering functional mRNA cargos as a gene therapy.
Native spike proteins tend to prematurely refold into a post-fusion conformation, which compromises immunogenic properties and prefusion trimer yields. mRNA vaccines therefore have slight modifications that simultaneously make the mRNA less immunogenic, and the spike protein it encodes more immunogenic. One way this has been done is to stabilize specific conformers through the addition of two strategic prolines to the code. However, more research is needed to fully characterize the fusogenic potential of stabilized spike proteins. Some vaccine manufacturers have eliminated the furin cleavage site from their mRNA construct in order to reduce potential residual fusion of a 2-PP stabilized construct.
The retrovirus is activated not by SARS virus but by spike protein.
All mRNA vaccines produce ample quantities of that spike protein in a very stable form that makes it very hard for cells to destroy it.
Very high concentration of spike protein either by a very bad infection or by vaccine jab will activate retrovirus in 20-30 percent of population with different genetics.
Also, once the dormant retrovirus present in all humans is activated by a specially designed and stable spike protein generated by vaccine code it starts multiplying and infecting many internal organs, including neurons and brain.
There could be no rational defense against that.