Cell EM function and Clinical Immortality

A premature baby would need to experience an bioelectromagnetic field sympathetic to itself, and one which would aid it in charging or enhancing its own field by entraining it upwards in intensity and amperage, or it would probably fail even in chemically perfect conditions.

Cells produce an em field of their own. The mother's em field probably interacts with the baby's em field in a way that helps sustain and grow the cells and systems of the baby, alleviating it of labor that its systems would have needed to perform on their own, as adults do, but for the support systems of the earth's ecoem field and our own panhuman social and living panecosystem fields.

This will require scanning of the em field of cells and groups of cells in an embryo and tailoring an artificial em field to support it as it grows.

When a zygote becomes fertilized, it senses the uniqueness of its own em field distinct from the mother [and father] and realizes itself as a new baby cell. This triggers existing circuitry inside the cell to execute, which releases appropriate proteins to cause the cell to produce certain developmental properties and divide at a certain frequency. Later this local information becomes specifically divided into organ types, and new plastic cells take cues from their surrounding em field and neighbors to recognize whether to turn into liver cells or skin cells. Furthermore, cell types may sense the field of all of a kind of cell, such as all the body's red blood cells, to determine if they need to produce more of said cell type. The red blood cell hz frequency in the body could be x, where x is relatively unique to the individual and has an accepted amperage for the system. The system of plasticity would detect this amperage level and if it fell below certain parameters, the cells would become predisposed to become red blood cells. This is likely inherent in every cell and found somewhere in its DNA. I wonder if em data causes cells' dna to be triggered and unrolled.

Detecting this field data could help us *safely* manipulate genes and test their functionality on a longer spectrum than a few generations. I also would love to examine the potential circuitry that can be produced by dna's resistance patterns within cells, and what those unique microfields would do within a cell or a cell group.

I also speculate that the appendix produces a field sympathetic and enhancing to 'good bacteria', but harmful or unrelated to bad bacteria. This electrical effect may also be a major way the body's immune system functions and a direct correlation between mood and immunity. [nobel prize for biology?] It also correlates to the white blood cell's direct system of using ~700nA to stun invaders to be flushed later, as field/signal immune system cooperation. This could allow us to engineer partial artificial immune system function. We can also produce room-sized or city-sized em field dynamics that are hostile to harmful microbes and beneficial to human growth and development, as well as mood. This potentiality has been demonstrated in the BBC article of the scientist who reproduced antedeluvian environmental conditions around piranhas which then displayed giantism, and likely later, veneration.

Em fields that trigger cell death for triggering lysosomes might exist, or cells might simply experience chemical trainwrecks causing lysis. If this is true, then by monitoring cell em health and undoing cell damage through immunology and em dynamic geometric tailoring we may be able to effect cell immortality. The system death of a human may also have such a trigger and also be detectable and preventable. This could potentially be the basis for clinical immortality.