Addenda, #1 DNA damage cationic lipids...

Those lipids required by the mRNA *vaccines* damage mitochondria, that cells are unable to repair (mitochondria can replicate if they are healthy, i.e., their own DNA, maternal originating exclusively, is undamaged).

Did Robert Malone not know this?

Being subjected to mRNA *vaccination* repeatedly is like being subjected to radiotherapy because of the toxicity of these lipids only already, without yet starting to talk about the payload they contain, where radiotherapy being based on radiant energy causes additive damage, i.e., essentially non-reversible, which adds up over time.

[M]itochondria play a key role in the process of programmed cell death — apoptosis. In this process signals cause the mitochondrial membrane to become permeable, which is a signal for activating the apoptopic pathway.

[T]he more functional mitochondria you have in your cells, the greater your overall health and durability.

[M]itochondria are the only cell components (other than the nucleus) to possess their own DNA. This means mitochondria have the ability to replicate and increase their number within a single human cell.

[M]itochondrial number and function determine human longevity. To put it simply, the more functional mitochondria you have in your cells, the greater your overall health and durability.

[Mitochondrial] dysfunction is a primary cause of age-related decline. In a revealing study, a team of researchers showed that muscle tissue of a 90-year-old man contained 95% damaged mitochondria compared to almost no damage in that of a 5-year-old.

[A] myriad of recent scientific reports link defective and deficient mitochondria to virtually all degenerative diseases including Alzheimer’s, type 2 diabetes, heart failure, and cancer.

#2 [to be continued]