Back to mitochondria some more interesting intel.
[link to en.wikipedia.org]
"Mitochondrial disease is a group of disorders caused by dysfunctional mitochondria, the organelles that generate energy for the cell. Mitochondria are found in every cell of the human body except red blood cells."
I found the above very interesting as pay attention the vampires in movies they just drink our blood which then the human body that remains becomes completely infected and a vampire.
So its amazing to find out that the only part of our bodies that is not infected by mitochondria/spider=mito snakes is our very blood!

[link to hplusmagazine.com]
"Although the vast majority of the approximately 3,000 mitochondrial genes are in the nucleus, mitochondria carry their own genome (DNA)(!reptilian dna!), encoding twenty-four different RNA types and thirteen polypeptides in humans. Interestingly, phylogenetic (the study of evolutionary links among organisms) analyses of the RNA and protein-encoding mitochondrial genomic regions show a eubacterial origin, indicating a common ancestral symbiont(virus!)."

And its amazing under the disguise they power our cells except our red blood cells(who powers those man? hahaha!) mutate our bodies and steal its immortality/lifeforce!
Jesus/medusa under the disguise of the savior and a lifegiver steals all life from his/her retarded victims!
Same draconian strategy in both cases man amazing!

Also an immortal body doesn't necessarily mean a forever preison for the soul when the soul remembers how to use a door handle! so it doesn't have to demolish the whole house to exit!

When someone erases your memories he can turn your own house into a preison! The car you drive to work too!
-How do i exit? screaming while kicking the glass!


[link to www.jci.org]
"Over the last decade, accumulating evidence has suggested a causative link between mitochondrial dysfunction and major phenotypes associated with aging. Somatic mitochondrial DNA (mtDNA) mutations and respiratory chain dysfunction accompany normal aging, but the first direct experimental evidence that increased mtDNA mutation levels contribute to progeroid phenotypes came from the mtDNA mutator mouse. Recent evidence suggests that increases in aging-associated mtDNA mutations are not caused by damage accumulation, but rather are due to clonal expansion of mtDNA replication errors that occur during development."

The clonal expansion reminded me agent smith from matrix! hahaha!

continue...