You hear people say they are grateful, what does that mean? To each person that means different things. In my opinion grateful means that life isn’t about your agenda it is about love. All there is is LOVE. Now you may think that is corny, but even when someone is pushing your buttons, it is love. They are bringing to the surface something deep within you that wants to be healed or released. That is love.
Being grateful is giving yourself over to a higher power than just your brain. We are all connected by the threads that our creator uses to make everything on this planet. When you go within and give gratitude for your life it sends a message of gratitude far and wide. So I ask on this day of Thanksgiving, to go within and give thanks for that which is love in your life.
thank you to Joseph Bennette for his research and thoughts.
RET activates deep brain structures involved in processing DNA within cells (amygdala, thalamus, hypothalamus, pituitary, pineal glands, etc.). This, it would appear, is most important during processing of the birth story and inner child stages (especially early childhood – ages 0-1).
Only within the past decade have scientists shown conclusively that the DNA molecule is modified by experiences of early childhood and pre-birth. RET can take advantage of that research by directly addressing the DNA and the cell control circuits (“blink it out of every cell…”). DNA does not change in a vacuum – it is controlled by thought energy at the cellular level. This means you can’t just tell a cell what to think using English – you must tell it using its own language, the language of chemistry. That chemistry is developed within brain regions directly affected by RET. During intense RET (rapid blinking, rapid verbal – RET immersion), brain chemistry is affected that directly addresses cellular structures that communicate chemically (re: cell membranes). RET tends to release stress – I believe RET can also be used to “reprogram” DNA for desired outcomes (client intention). Here’s the process as I see it:
RET intense blinking activates central brain structures involved in chemical reactions (pituitary, thalamus, pineal)
Chemicals induced by RET course through the body’s circuitry – but are basically just “there” until activated by electrochemical commands in cell membranes
Verbal instructions to “blink it out of every cell” activates release chemistry at the cellular membrane level – initiating a cellular discharge and setting up DNA for change
Verbal instruction to “blink it out of the DNA” activates release chemistry at the DNA level – changing DNA slightly
Verbal instruction to “incorporate your intention into every cell and the DNA” might then reprogram the DNA to further solidify the client’s intention by imprinting the intention into their DNA
RNA transcribes the DNA instructions into restructuring the physical body by spreading the new DNA message – thus enabling permanent change
Gene Vital To Normal Brain Function Modified By Early Life Experience
30 Sep 2010
Early life stress, such as an extreme lack of parental affection, has lasting effects on a gene important to normal brain processes and also tied to mental disorders, according to a new animal study in the Sept. 29 issue of The Journal of Neuroscience.
In the last decade, researchers have found evidence that experiences can alter the form and structure of DNA, an effect known as epigenetics. Because these changes affect genes, events early in life have the potential to make a lasting impact on behavior and health. Recent studies focused on cancer and obesity have already shown the power of epigenetics.
In a study led by Tie-Yuan Zhang, PhD, of McGill University, researchers investigated whether these changes might apply to the activity of genes in brain regions that control neural function and mental health. The authors explored how differences in a mother’s attention affect the GAD1 gene, which controls the production of a chemical vital to brain cell communication called GABA. Research indicates that GABA helps to regulate emotion, and that people with schizophrenia may have GABA deficits.
The authors studied the maternal behavior of rats specifically bred to be either extremely caring or rarely affectionate. They found when the baby rats that were seldom touched grew up, specific regions of the DNA that controls the GAD1 gene were obstructed, likely leading to smaller amounts of GABA. On the other hand, adult rats coddled in the extreme as pups showed increased GAD1 gene production.
“A critical feature for the effect on gene GAD1 is that the immediate influence of maternal care is limited to a short period following birth, but the resulting changes are long-lasting, even into adulthood,” Zhang said.
These findings suggest that the early life environment can drive molecular changes that affect brain function and might determine a child’s predisposition to mental illness.
“We already knew that maternal care determined the stress responses of an offspring through a similar process, but this is the first time maternal care has been shown to link, via epigenetics, with a key enzyme that causes a major human disorder,” said Jonathan Seckl, MD, PhD, of The University of Edinburgh, and an expert on the molecular process of hormones.
The research was supported by the National Alliance for Research on Schizophrenia and Affective Disorders and by funding from the Canadian Institutes for Health Research and the National Institute of Child Health and Development.
