Heather Rae, Functional Health Practitioner
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health coach, specializing in alchemical biochemistry, genomics, anatomy, and bio-energetics
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GenomicInsight Powered by Opus23 Explorer includes:
• An interactive dashboard allowing practitioners to curate results from select areas of health including detoxification, cardiovascular health, methylation, HPA-axis, metabolic syndrome, mitochondrial health, pharmacogenomics, nutrigenomics, estrogen metabolism, sex hormones, aging, and autoimmunity
• Medical datasets and biomedical literature updated in "real-time," including PubMed
• Evidence-based therapeutic recommendations
Forwarded from Judy MikovitsFAKE
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THE THERAPIES THAT DR MIKOVITZ DESCRIBES ARE AT THE HEART OF FUNCTIONAL HEALTH. However, not everyone will respond well to things like glutathione (the master anti-oxidant comprising NAC (cysteine)-glycine-glutamate) KNOW YOUR DNA, YOUR TOXIN AND NUTRIENT LEVELS, PH/VOLTAGE AND CELLULAR LIPIDS, and SUPPORT YOUR TERRAIN with functional genomics.
For example, people with variants in genes that manage neurotransmitters (brain hormones, you might call them) such as dopamine may have a negative response to QUERCETIN.
AN EXAMPLE OF TOPLINE FINDINGS OF A CLIENT'S ORGANIC ACIDS AND DNA TESTS:
• Some indication of toxic burden using up nutrients like B6, B12, NAC, Vit C which are all low
• High dopamine (need B6, copper, Vit C); toxins will compete with dopamine clearance for those same nutrients; high dopamine reflects those dopamine-related clearance genes like COMT
• Low serotonin (reflects the genes related to making serotonin like MAO-A)
• High oxalic (21) from diet (high oxalate foods) or molds (fusarium) and possibly exacerbated by a few genes that clear bile/oxalates
• High fats (from diet?)
• Methylation, toxic exposure (59); methylation genes look good but B12 genes (TCP/GIF) could use support with B12 supplementation
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HYDROGEN & DISEASE ... pH is just one factor (alkalinity of the cell); hydrogen is a bigger deal.
“The focus should not go on killing viruses, but rather on changing the blood’s electrochemical properties to make viral multiplication impossible.”
VACCINATION IS HEAVY ARTILLERY THAT DESTROYS EVERYTHING with « collateral damage ». Modifying the « bioelectronic terrain » suppresses a condition that is vital for viruses to multiply. These may enter the body, but they cannot multiply in a reductive terrain.”
THE GENOME OF EACH INDIVIDUAL IS IN A STATE OF CONSTANT TRANSFORMATION. https://odysee.com/@DeansDanes:1/Healing-Conference-2021_Stefan-Lanka:a @38 Lanka explains "old virology" vs "new virology" which came into being in the 1950s with Enders. Old virologists knew that viruses were the output of dead and dying cells (bacterial macrophages ... bacteriophages ... the end-product of proteins spurred by catalytic nucleic acids) and NOT pathogens. Which really sucks if you want to scare the shit out of people with viruses and sell vaccines.
PERPETUATING THE IDEA OF "VIRUS AS PATHOGEN" IS BIG (BIG) BUSINESS. OBVIOUSLY.
VIROLOGY UNDER THE MICROSCOPE ... CORONAVIRUS IS MADE UP IN A COMPUTER, NEVER FOUND (ISOLATED) IN A HUMAN BEING. Every wonder why there is, in this world at this time of a 'pandemic,' no test for a "spike protein" in an real living human being? Just a PCR test looking for a fragment of genetic code that can be found in a fruit?
WHEN MEDICINE BECOMES BIG BUSINESS ... PUBLISHED IN 1976 ... "The medical establishment has become a major threat to health."
VIRUSES ARE A "MENTAL CONSTRUCTION" OF BITS OF GENETIC MATERIAL, CREATED 'IN SILICO' (IN A COMPUTER) Enders did not use controlled experiments; he added antibiotics and chemicals and starved the tissue and proclaimed its demise was due to the unseen, unisolated 'viruses' (which we know were simply the end results of killing tissue with toxins and malnutrition). It's ass-backwards, illogical, and dare we say, UNSCIENTIFIC.