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Christian Bogner @MakeAmericaHA on x 2106 followers
Created: 2025-07-18 18:38:56 UTC
Emerging clinical insights, sophisticated laboratory analyses, and the outcomes of precision interventions with our patients over many years are converging on a profound revelation: the genetic status and functional capacity of the MAO (monoamine oxidase) enzyme fundamentally stratify children across the autism spectrum. This singular enzyme, often overlooked, serves as a critical gatekeeper between neurological balance and chaos.
When MAO function is genetically compromised or sluggish, the body struggles to degrade powerful psychoactive compounds, e.g. DMT, bufotenin, serotonin, and other tryptamines, all of which are synthesized within the microbiome. The result is an unchecked accumulation of these consciousness-altering molecules, driving severe forms of autism (to the observer) marked by profound detachment from reality, as if the child were perpetually submerged in a relentless, endogenous psychedelic state.
Conversely, when MAO activity is accelerated, these psychoactives are swiftly neutralized. The brain becomes starved of the vibrancy and color they might have otherwise imparted, yielding a high-functioning yet affectively monotone phenotype, high intelligence encased in a grayscale world with devoid (or at least less) emotional resonance or sensory depth.
While myriad toxins, LPS, glyphosate, aldehydes, ammonia, oxalates, mycotoxins, heavy metals, certainly erode neurological integrity, it is this MAO-serotonin-tryptamine-DMT axis that emerges as the fulcrum of neurochemical equilibrium. Understanding and modulating this axis holds the potential to recalibrate perception, cognition, and connection for those on the spectrum, bridging worlds otherwise sealed off by biology.
@HHSGov @SecKennedy @NIHDirector_Jay @NicoleShanahan @ChildrensHD @lifebiomedguru @DrSuzanneH7 @BusyDrT @DrOz @joeroganhq @elonmusk @MedMAPS
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