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☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆

@DrJackKruse

I began with Becker's work and for 40 years I update his work. I was lucky to meet him several years before he died and sat down with him to talk about what I found. Here is a small snippet of what I shared with him. Bioelectricity is down stream the real story in biology. We need to understand life before it become a DC electric current for morphogenesis and regeneration. I have used Becker's work to re-defined Life as a Light-Driven Rate Machine. Since the GOE, the competitive advantage of complex life has been its ability to maintain Isotopic Coherence. Disease is "Quantum Retardation" which remains a chronic loss of the ability to produce DDW, leading to a collapse of the protein semiconductor network and a return to the high-entropy, pre-oxygenic past. Dehydrating melanin is the the best way to lose the DC electric signals in mammals. Here is a summary of the basics of what I outlined. Mammalian complexity (body plan) is a function of isotopic purity and semiconductor coherence. Becker got this idea from Szent Gyorgi in his Budapest speech in 1941. In 20 yrs Becker proved this thesis true. I then decided to go deeper and figure out how these semiconductors operate in health, disease, and morphogenesis. I began using Turning math paper on morphogenesis from the 1950s. My model sits on the shoulder of Becker's work and Turing's math. It provides a definitive biophysical answer to the transition from simple life to complex eukaryotes: I began by framing Cytochrome c Oxidase (CCO) as the primary "isotopic gatekeeper," my decentralized thesis identified the specific mechanism that separates a healthy, high-performance proteome from a diseased, Warburg-shifted one. Here are three summary slides of the ideas I shared with him below from my notebooks. The last idea is how regeneration and morphogenesis proceeds based on my intrepretation of his work. The Recovery Pathway of Mammals: HKDC1 and Mitophagy I mentioned the HKDC1 pathways and how mitophagy completes the "maintenance" cycle of my decentralized thesis: We Eecycle the "Heavy" Hardware: Mitophagy identifies and clears mitochondria that have become deuterium-laden. This is linked to its size and shape changes. Restoring the Matrix Pool = is restoration of Energy transformation: By recycling these damaged components, the cell attempts to maintain its internal DDW pools. The DDW Test: This explains why drinking DDW acts as a "quantum bypass." It manually lowers the D-burden, allowing CCO and the VDR (Vitamin D Receptor) to function again on the IMM, restoring the DC current and re-enabling the "Cambrian" complexity of the cell. Without hydrated melanin there is no one trillionth of one ampere of current that turned Becker's RBCs back into their primitive forms to regenerate bone as he showed in his experiments. <a target="_blank" href="https://twitter.com/BrianRoemmele/status/2012002504783827423" color="blue">x.com/BrianRoemmele/…</a>

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