1. When inflammation is present in the brain (excess protons or too few electrons), the three fundamental laws of nature are altered in our tissues. This causes them to decrease their ability to deliver higher levels of oxygen to the neocortex below to maintain proper cognitive function. This decreased oxygen density over specific portions of the neocortex acts to limit its function, relative to other areas of the neocortex by changing proton conduction.
2. This single event uncouples mitochondrion in the neocortex and it raises that neuron’s basal metabolic rate. A chronic raised basal metabolic rate leads to cerebrovascular diseases because it increases mitochondrial respiration and the amount of physiologic work a cell has to do. This is why ALL brain diseases are associated with atherosclerosis at a core level. This is precisely how leptin resistance causes a neuro-cognitive decline in humans.
3. The CSF around the hypothalamus becomes less dense and has a higher temperature with higher levels of cytokines in it, causing us to lose energy/info to the environment. We’ve known for a long time that only two things lower metabolic rates in living things, strong solar stimulus, and cooling. This changes the hydrogen bonding network possible in CSF. The problem for medicine is that these scaling laws of energy flux have not made it into clinical medicine as yet. This loss of energy means less oxygen is delivered to the neurons in the hypothalamus, which is designed to work optimally when there is harmony and energy balance in humans.
4. This is why in EMF 2, I told you the leptin receptor was an ‘account’ of photons, protons, and electrons. All bits of matter that make things up roughly have equal numbers of electrons and protons. The number of photons varies. The basics of what most people forget are that if this were not so, there would be an excess of a positive or negative charge, and this would create a massive force pushing all the excess charge out, leaving behind a core group of neutral charges.
5. When sunlight moves electrons/protons in us with the energy in light waves it alters the arrangement of our bio-molecules and changes their thermodynamics. A change in an arrangement is a change in the "information" in the system. Different molecular arrangements have different energies/information associated with them. This difference in energy/info is how bio-molecules are quantized to light frequencies. It also explains how metabolic networks became coupled to terrestrial solar frequencies.
6. The brain evolved, I believe to order this process using solar frequencies between 250-780 nm. The circadian signals are how that energy harmony is translated from the outside world to the inner workings of biochemistry. When these signals are off for any reason at all, we begin to lose energy to our environment by emitting black box radiation from our bodies. Essentially, we are losing captured sunlight, and this decreases the amount of physiologic work a cell can do. This means in illness cells are losing energy at the vibrational or electronic level and can no longer remain a dissipative structure.
7. Prigogine defined dissipative structures and their role in thermodynamic systems far from equilibrium, a discovery that won him the Nobel Prize in Chemistry in 1977. In summary, Ilya Prigogine discovered that the importation and dissipation of energy into chemical systems could result in the emergence of new structures (hence dissipative structures) due to internal self-reorganization. In his 1955 text, Prigogine drew connections between dissipative structures and the Rayleigh-Bénard instability, and the Turing mechanism. Prigogine's theorem is germane to these ideas.
Mitochondria are dissipative structures in cells, but not the only ones. They transform energy and create order from the disorder in light energy they use to operate. The water mitochondria create is probably the single most important dissipative structure that life is based upon in cells. According to Prigogine, determinism loses its explanatory power in the face of irreversibility and instability in dissipative systems. This is a major departure from the approach of Newton, Einstein, and Schrödinger, all of whom expressed their theories in terms of deterministic equations.
8. Indeterminism is the opposite of determinism and is related to chance. Chance is related to probability. In science, most specifically quantum theory in physics links directly to probability and not cause and effect. Indeterminism is the belief that no event is certain and the entire outcome of anything is probabilistic. Heisenberg's uncertainty principle and the "Born rule", proposed by Max Born, are often starting points in support of the indeterministic nature of the universe. Indeterminism is also asserted by Sir Arthur Eddington and Murray Gell-Mann. Indeterminism has been promoted by the French biologist Jacques Monod's essay "Chance and Necessity". Ilya Prigogine argued for indeterminism in complex systems.
9. At life's genesis chaos has to gain order. Dissipative structure theory really aims to solve this problem for biology by using physics.
Dissipative structure theory led to pioneering research in self-organizing systems, as well as philosophical inquiries into the formation of complexity on biological entities and the quest for a creative and irreversible role of time in the natural sciences.
There is a well-known theorem of minimum entropy production derived by Prigogine, which states that entropy exported from a system reaches a minimum, or becomes zero, at thermodynamic equilibrium and at steady states close to thermodynamic equilibrium. Prigogine's theorem is a direct consequence of Onsager's reciprocity relationship which holds at steady states close to thermodynamic equilibrium. The principle of internal entropy compensation, is in addition to, and implies the principle of minimum entropy production, and may even be valid in regimes far from thermodynamic equilibrium.
10. He had some very interesting things to say about TIME in his work and Nobel Prize speech. You should watch it sometime. I think they are key to understanding circadian biology and timing. All of our time reversible equations in physics created by Newton, Einstein, and Schrödinger describe a simplification of what actually occurs in nature. We live our lives with eyes blinkered, dismissing reality as the exception to our neatly formed approximations of what time really is.
11. Time is a critical issue for dissipative systems. While most current thermodynamical analyses used in biology completely ignore space-time structure, the “thermodynamics of organized complexity” applying to living systems depends WHOLLY on space-time heterogeneity, which allows ‘free’ variation of microscopic states within macroscopic constraints. THIS DEFINES WHAT A MITOCHONDRIA WAS DESIGNED TO DO AND TO BE IN A VARYING EMF FIELD CREATED ON THIS PLANET by the sun.
12. His theories offer us another possibility of some form of enthalpy-entropy compensation, as mentioned in my work in connection with enzyme catalysis, so that coherent energy is conserved in organelles in the cell, with no entropy generated. This is maintained by the atomic organization of atoms in a cell. The system could be arbitrarily far away from equilibrium, so long as, at some sufficiently macroscopic space-time of interest, the overall balance is attained, and the net entropy production of the system either vanishes or reaches a minimum.
The internal balance of entropy production means that the system maintains its organized heterogeneity or dynamic order. It is in turn dependent on energy flow being symmetrically coupled and cyclically closed over the system as a whole. In other words, it depends on the validity of Onsager's reciprocity relationship in systems far from thermodynamic equilibrium.
13. Circadian time stamping is done AFTER DNA is translated. This implies that the genetic code is not the primary issue in diseases and health creation. Time stamping is due to his theorems of Prigogine. Circadian time stamping also puts undue stress on our cell’s mitochondrion and they begin to act less like a part of our cellular design and more like a captured slave bacteria that they really are. Since a mitochondrion has bacterial origins, most of man’s chronic diseases look like infectious diseases at the core. This is deceptive because this viewpoint does not go down to the most critical level to understand how subatomic charged particles behave at small scales with the electromagnetic forces that light waves can impart to them.
14. One of the hallmarks of the living system in cells is that they are exquisitely sensitive to specific, weak signals. Most of these signals are electromagnetic in nature. The human eye can detect single photons falling on the retina, which pass information directly to the SCN and all its mitochondria. This retina is where the light-sensitive photoreceptors in cells send out an action potential that represents a million-fold amplification of the energy in the photon. This defines what a non-linear stimulus is. Some of you know it by the butterfly effect.
It is not just a property of the central retinal pathways. The entire system is a plasma or syncytium of excitable matter ready to react to the environment's EMF signals. Similarly, a few molecules of pheromones in the air are sufficient to attract male insects to their mates. This sensitivity is characteristic of all parts of the system and is a consequence of the energy stored = related to the AMO physics of organization.
No part of the system has to be pushed or pulled into action, nor be subjected to mechanical regulation and control. Instead, coordinated action of all the parts depends on rapid intercommunication throughout the system because of how it is built to react to light. The organism is a system of “excitable media” (syncytium) — excitable cells and tissues poised to respond specifically and disproportionately to weak signals because a large amount of energy stored everywhere automatically amplifies weak signals. These signals often direct things in cells into macroscopic actions. This is how order is built from chaos in a dissipative structure described by Prigogine's theorem.
15. Lesson over.
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The main risks related to stereoisomers arise if a supplement contains an incorrect or mixed (racemic) form of a chiral compound:
Different Biological Effects: One stereoisomer may be active and beneficial, while the other may be inactive or even harmful. For example, the body primarily uses L-amino acids, and D-forms are often less bioavailable or utilized differently.
Toxicity: In the pharmaceutical world, the wrong enantiomer has, in some historical cases, shown different toxicity profiles, including teratogenicity or organ-specific harm.
For example:
The thalidomide tragedy of the late 1950s and early 1960s. This historical case points out what I am referring to in the peptide world or amino acid world of supplements. You never hear the food guru or peptide gurus tell you about the history of this risk so here you go.
Thalidomide was sold as a racemic mixture (containing equal parts of two mirror-image molecules, or enantiomers) and marketed as a safe sedative and an effective treatment for morning sickness in pregnant women. The different enantiomers had drastically different effects:
The (R)-enantiomer was the effective sedative with the desired therapeutic effect.
The (S)-enantiomer was a potent teratogen, meaning it caused severe birth defects in developing embryos, particularly affecting limb development (phocomelia), as well as eye, ear, heart, and internal organ development.
An estimated 10,000 to 20,000 infants in 46 countries were affected by these deformities. Many believe as I do these numbers are way under reported.
Crucially, even if the "safe" (R)-enantiomer had been administered alone, it would have been ineffective in preventing the harm because the human body's metabolic processes convert (R)-thalidomide into the toxic (S)-enantiomer, and vice versa, in a process called chiral inversion.
This disaster was a turning point in pharmaceutical regulation, leading to much stricter drug testing protocols and an increased understanding and focus on the importance of stereochemistry in drug development and safety testing. This was never applied to the peptide markets FYI. You have to TRUST that the lab or pharmacy does these tests.
2. More to worry about? Some peptide users in my client have developed amyloid changes. What did I tell them about continued use?
You might create a neurodegenerative disorder in your brain. Why?
Amyloid Beta (Aβ) peptides: In vivo, Aβ peptides, linked to Alzheimer's, can be found with D-amino acids (specifically Asp and Ser residues), indicating that a natural inversion process occurs, which affects their aggregation properties. This is an example of chiral inversion. This kind of freaked them out. When they questioned the lab/pharmacy and longevity docs who gave them this stuff communication completely shut down.
Decentralized medicine aims to educate not induce fear.
3. Why did I stop using NSAIDs in my patients around 2000? I read about homochirality and where it comes from. The physics of the cosmos.
Non-Steroidal Anti-Inflammatory Drugs (NSAIDs): While not peptides, a prominent example in pharmaceuticals (like ibuprofen) involves chiral inversion. The inactive (R)-enantiomer is metabolically converted into the active (S)-enantiomer by hepatic enzymes in the body, showcasing a clear biological pathway for inversion in a non-peptide context.
Tissue polarization by artificial light turn the matrix of mitochondria into a deuterium-gated racemization factory, turning mitochondrial proteins into mirror-image versions that:
a. reverse CISS spin filtering,
b. invert local PV asymmetry,
c. emit optically “backwards” UPEs that neighboring healthy cells can no longer read correctly,
d. and render affected cells invisible to immune surveillance by NK cells (D-peptides are non-self to TCRs that evolved under L-only rules).
2. COVID was more than a virus—it was a Parity Violation inversion, hijacking the iron at the center of life’s light engines. By disrupting heme, it dimmed the internal sun of billions. Homochirality allows for the precise folding and functionality of complex structures like mitochondrial matrix, proteins and RNA/DNA, which is essential for the high energy efficiency of aerobic life.
A "global change in homochirality" in a body was changed by the spike protein and was indeed catastrophic to the compliant, on an oxygen-dependent food web because ALL of that machinery of life relies entirely on this specific asymmetry.
3. Cytochrome C Oxidase is the key Parity Violation gatekeeper because Normal apoptosis is triggered when cytochrome C (a heme protein in the ETC) is released from the inter-membrane space into the cytosol.
Many do not know Cytochrome C Oxidase is exquisitely chiral (L-amino acids, PV-selected structure). Its release binds Apaf-1 in a stereospecific way to form the apoptosome → caspase cascade → orderly cell death.
Without an intact apoptosis SV 40 promotor would promote explosive turbo cancer formation in the compliant among many other PV diseases. It would mimic an extinction event to mirror the 5 we've already had.
In most cancers, the Bcl-2 family (anti-apoptotic) blocks cytochrome C release, or the apoptosome is mutated. No cytochrome C release = no chiral "death signal" = You are getting a turbo cancer.
Wondering if you'd be able to break down what happened after I took Venlafaxine (Effexor) a few years ago and if there's any specific things needed to be done to hopefully repair any damage.
After what I believe was a spontaneous CSF leak that happened one night and started all my chronic issues I was diagnosed with vestibular migraine around 3 months later.
Venlafaxine 75mg was indicated for this so I was on it for around 12 months (give or take the 3 months wean I did).
Within 3 weeks my emotions went numb, I lost my libido, erections and ability to pretty much feel love or any strong emotion. There was a very definite and obvious "change" but I believe I still had the ability to focus and enjoy hobbies etc.
After deciding to taper off, I would get brain zaps and all the other jazz that comes with it. After fully tapering, I was then introduced to anhedonia. Unable to feel or enjoy anything, unable to focus on anything for too long without getting the irritable and feeling like I need to do something else etc. Essentially feel there's been a permanent change since starting this.
This has improved slightly but not even close to where I'd like to be. Add all the daily brain fog, memory lapses etc and my brain is running on empty.
Does this need anything specific additional to the core light, water & magnetism?
Listening to this months webinar you mentioned accutane extending recovery from 6 months up to 5 years. This prompted me to ask this question and about my accutane use in the future as this is a huge jump in recovery time and shows how powerful these drugs are.
Thanks,
Ja$%^
3. Reasons Why Venlafaxine Could Cause Issues, Based on My Decentralized Thesis
My thesis posits that life's core "code" resides in conserved correlations of phase, spin, and topology, geometric invariants that maintain coherence beyond mere voltage gradients. Man-made electromagnetic (EM) pollution disrupts this coherence, leading to health risks like aging, cancer, and failed regeneration. Voltage is merely a "courier," while true memory and form emerge from photonic organization of spin and topological symmetry. Venlafaxine, as a synthetic molecule introduced into this already polluted EM environment, would act to exacerbate disruptions by interfering with biological EM phenomena. Below, I list hypothesized reasons grounded in its structure, spectra, pharmacology, and potential EM interactions. These are imaginative extensions based on my published framework, drawing from known drug effects and bio-EM principles (e.g., biophotons, ion flows, and field coherence), while acknowledging that direct studies on venlafaxine-EM-biology intersections are limited because BigHarma isn't going to harpon its own product with truthful decentralized science.
1. I just gave a talk to a group of medical students..........Here was my only slide.
2. Here was the substance of the talk.
The talk was a sobering discussion for me, yet it empowered my reflection on navigating a world where societal dogma often clashes with truth.
I explored how civilization rewards comfortable lies while penalizing painful truths.
3. Now we’ll focus on the hope for humanity amidst this tension, the challenges of earning a living, and our personal choices in deciding where we fit into this complex landscape.
What don't sunglass and eye glass manufacturer's know? Polarized light and lenses are used as a tool to detect and measure the tiny effects of Parity Violation in atoms and molecules, where the weak force causes a slight "handedness" in physical systems that are otherwise mirror-symmetric.
The core link is that the weak force's violation of parity symmetry leads to a mixing of atomic or molecular states that should, under normal circumstances (governed by the parity-conserving electromagnetic and strong forces), have a definite, opposite parity. This mixing is extremely small but results in two primary observable effects involving polarized light. It affects water networks and all proteins that interact with the polarized light.
Note: all artificial sources of light are POLARIZED.
When linearly polarized light passes through an atomic vapor or a chiral medium like the human eye, its plane of polarization rotates slightly. The amount of rotation is related to the degree of parity violation in the atoms distal to it.
Materials exposed to the weak interaction can show a minuscule difference in how they absorb left-handed versus right-handed circularly polarized light. Why is this a big deal in my human patients?
Stellar masses are designed to use you as their lens. This is why DNA codes only for semiconductive proteins that all have absorption and emission spectra.
Parity vioation in your tissues explain life's universal preference for L-amino acids and D-sugars, a puzzle since Pasteur's 1848 discovery of molecular chirality. when you wear lenses in front of your eyes or bath in light man makes you just broke a fundamental law of Nature and it always leads to DISEASE your doctors are impotent to repair.
2. Just how big a deal is this? This is why the meat head carnivores and the longevity doctors need to be ignored. It could lead you to a nasty disease.
3. The weak force interacts with particles based on their "handedness" (helicity), preferring certain orientations over their mirror images. In atoms, this causes a tiny amount of mixing between electron orbitals of opposite parity (e.g., s and p orbitals).
Y'all know that DNA has a helix structure huh? Cause the guys above did not use that as part of the centralized adivce for their clients. Rosalind Franklin showed us this in 1951.