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''Because we have known nothing else in our recent history and have erased memories, humanity is unaware that we have existed with severely dysfunctional Mitochondrion.'' | ''Because we have known nothing else in our recent history and have erased memories, humanity is unaware that we have existed with severely dysfunctional Mitochondrion.'' | ||
This is a direct result of the Mother’s DNA, magnetic principles and proton structure extracted from this earth and a synthetic alien version of “Dark Mother” that was put into the planetary architecture to mimic its functions. Humanity has been without its true [[Mother Arc|Mother principle]] functioning on the planet and evidently this is recorded in the cells of our Mitochondrial DNA. This event has been described many times as the [[NAA]] invasion of [[Planetary Logos]] through controlling the magnetosphere and magnetic field. | This is a direct result of the Mother’s DNA, magnetic principles and proton structure extracted from this earth and a synthetic alien version of “Dark Mother” that was put into the planetary architecture to mimic its functions. Humanity has been without its true [[Mother Arc|Mother principle]] functioning on the planet and evidently this is recorded in the cells of our Mitochondrial DNA. This event has been described many times as the [[NAA]] invasion of [[Planetary Logos]] through controlling the magnetosphere and magnetic field.<ref>[http://www.energeticsynthesis.com/index.php/resource-tools/news-shift-timelines/2482-sophianic-body-correction Sophianic Body Correction, July 2014]</ref> | ||
==Mother’s Mitochondrial DNA== | ==Mother’s Mitochondrial DNA== | ||
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Mitochondrial diseases are from genetic mutations imprinted into the DNA sequences. [[Artificial Machinery|Artificial architecture]] placed into the planet, such as alien machinery, with intention to make genetic modification to usurp the Mother’s DNA, manifested DNA mutation and DNA damage to all species. Mitochondrial diseases take on unique characteristics of blocked energy in the body because of the way the disease accumulated through inherited maternal genetics in ancestral bloodlines. Mitochondrion is critical for every day cell function and energy metabolism which also leads to spiritual progression of soul and oversoul (monad) embodiment. Mitochondrial disease reduces effective overall energy production for the available body-consciousness energy, stunting human development and spiritual growth. Thus, the body ages and gets diseases faster; the personal energy is deactivated thus depleted. This severely limits the amount of usable energy available for the brain development and all neurological system functions. | Mitochondrial diseases are from genetic mutations imprinted into the DNA sequences. [[Artificial Machinery|Artificial architecture]] placed into the planet, such as alien machinery, with intention to make genetic modification to usurp the Mother’s DNA, manifested DNA mutation and DNA damage to all species. Mitochondrial diseases take on unique characteristics of blocked energy in the body because of the way the disease accumulated through inherited maternal genetics in ancestral bloodlines. Mitochondrion is critical for every day cell function and energy metabolism which also leads to spiritual progression of soul and oversoul (monad) embodiment. Mitochondrial disease reduces effective overall energy production for the available body-consciousness energy, stunting human development and spiritual growth. Thus, the body ages and gets diseases faster; the personal energy is deactivated thus depleted. This severely limits the amount of usable energy available for the brain development and all neurological system functions. | ||
Depletion of energy reserves for building brain and neurological development contributes to the spectrum of autism, neurodegeneration and other brain processing deficiencies. Defects in mitochondrial genes are associated with hundreds of “clinical” diseases prevalent in primarily blood, brain and neurological disorders. | Depletion of energy reserves for building brain and neurological development contributes to the spectrum of autism, neurodegeneration and other brain processing deficiencies. Defects in mitochondrial genes are associated with hundreds of “clinical” diseases prevalent in primarily blood, brain and neurological disorders.[http://www.energeticsynthesis.com/index.php/resource-tools/news-shift-timelines/2482-sophianic-body-correction Sophianic Body Correction, July 2014]</ref> | ||
==References== | ==References== |