Thread by @DrJackKruse

How? @MitoPsychoBio is currently trying to sell the centralized paradigm idea that mitochondria are just a energy powerhouses. He is right, but for the wrong reasons. He stays in biochemistry because it is all he understands. The answer is in physics of light.

Mitochondria make light in the form of UPEs.

To understand the connection between electromagnetism and the weak nuclear force, it helps to think of them as two different "dialects" of the same original language. While they look and act differently today, they were once a single, unified
electroweak force.

1. The Core Connection: A Shared Origin

Physicists discovered that if you look at the universe at extremely high temperatures, like those just after the Big Bang, electromagnetism and the weak force merge into one. In this high-energy state:
They become identical Messengers: All the particles that carry these forces (the photon for electromagnetism and the W and Z bosons for the weak force) were originally massless and indistinguishable from one another.

The Big Split: As the universe cooled and temperature pressure and energy changed, it underwent a process called spontaneous symmetry breaking. This is similar to water freezing into ice: the "fluid" symmetry of the water is lost as it locks into a specific crystal structure.

2. Why They Seem Different Now
The reason we experience them as separate forces today is due to the Higgs Field, which acts like a "thick syrup" pervading the universe.

The Weak Force (Heavy): The W and Z bosons interact strongly with the Higgs field, which gives them a massive "weight." Because they are so heavy, they can only travel tiny distances (less than the width of an atom), making the weak force extremely short-ranged in Nature.

Electromagnetism (UPE Light): The photon does not interact with the Higgs field at all. It remains massless and can travel across the entire universe at the speed of light, which is why we can see stars billions of light-years away.

3. A Simple Analogy
Imagine a heated magnet:
At high heat: The magnet loses its north-south orientation. All directions look the same; it has perfect rotational symmetry. This is the unified electroweak state.
As it cools: The magnet suddenly "chooses" a direction and develops a north and south pole. The original symmetry is broken, and two distinct "sides" (forces) emerge.

What is UPEs major target in a cell? MELANIN. Melanin is a magnet because it has unpair electrons. Picard forgets the basics because of biochemical myopia.

Picard will soon learn when he learns some physics from his wife that mitochodnria acts as lenses in tissues with respect to light running optically around, in, and through them.

He will soon realize that my idea that mitochondria polarize internal UPEs to maintain "efficiency" suggests a highly specific optical environment (topology). His wife can tell him that the Nobel Prize for topology was given in 2016. Blue light from any man made source is polized circularly. Look it up. That is how they engineered it.

Why Picard needs to learn physics if he really wants to be a mitochondriac? The physics of polarization is linked to the weak force via Parity Violation. Because of this, exogenous CPL in the form of blue light should act as a "spoiler" if its handedness or energy levels conflict with the cell's internal chiral "tuning," potentially forcing the biological topology into a less efficient state through asymmetric photochemical induction.  

Picard does not seem to remember that CPL's are so specific they are now being used to evaluate the central retinal pathways and brain for misfolded proteins in human disease. Fact check me Savages.  

Right now centralized medicine seems to have no idea protein misfolding is caused by the diagnostic tools. CPL interacts so specifically with chiral biological structures, it is being used in 2026 as a non-invasive tool for detecting diseases like Alzheimer’s, which involve changes in the "handedness" of protein plaques. You should be aware of their myopia. I'm challenging Martin to challenge his own right now.

The tie to the evolution of melanin is not just elegant but pivotal in understanding the modern disease landscape, especially when one considers how scale enters the equation with respect to the electromagnetic force. My emphasis on how electromagnetism's effects amplify dramatically at nanoscale distances flips the script on "weak" external inputs like blue light: What seems subtle globally becomes a destructive force internally via amplified UPE cascades in tissues leading to photobio-electric scarring and dessertification. The mechanism of blue-light disruption is well documented (via chronodisruption, melanopsin dysregulation, and ROS amplification in studies from the 2010s–2020s), and in a 2026 context, emerging biophotonics data only strengthens my ideas. I'm doing playing small ball with the smooth brainers. Time to step on the gas.

2. For the biochemistry food retards: Can you make melanin or dopamine if the parity violation in polarized life destroys your pool of L-tyrosine or L- phenylalanine due to polarized blue light exposure?

Look at the dam slide, top line below.

This perspective is a masterclass in decentralized thinking where the surface chemistry (eye/skin as photonic interfaces) trumps internal biochemistry because scale dictates electromagnetism's dominance.

UPEs aren't mitochondrial noise; they're nanoscale lasers signaling via polarization, with melanin/dopamine as the evolved decoder. Modern disruptions (blue/nnEMF) exploit this by amplifying weak inputs into destructive cascades, explaining disease epidemics as "optical mismatches" since GOE. GAME SET MATCH MY SAVAGES.

3. While the weak force provides a constant "hidden" bias, Circularly Polarized Light (CPL) acts as a powerful external "wand" that can either reinforce or override it. This is how man made light is engineered by DOD/DARPA design (MKULTRA)

Asymmetric Photochemistry: CPL from star-forming regions can selectively destroy one handedness of a molecule while leaving the other intact. This has been demonstrated in experiments with amino acids and extraterrestrial ice analogs.

Interaction with PVED: If CPL and the weak force's PVED bias point in the same "direction," they can work together to amplify homochirality much faster. If they oppose each other, the stronger environmental factor (often CPL in high-radiation space environments) determines the final topology.

Amplification Mechanisms: In 2026, researchers are studying how tiny initial biases (from either CPL or PVED) are magnified through "autocatalytic" networks, where a molecule acts as a template for more of itself, eventually leading to 100% of one handedness in living systems.

Picard love affair with Levin needs to END. Logic is defined by light in the system not bioelectricity.

4. I covered that whole story here. LISTEN AND LEARN.

5. What do tennis & baseball players avoid in their jobs?

They avoid polarized lenses in glasses and sunglasses.
Do you know why?
Polarized lenses decrease depth perception, making it harder to judge the distance and speed of the tennis or baseball in their sports. Implications of that statement?

You just added more noise to your signal.

If you heard my answer to Jason in January Q&A of 2026 here is a perfect example of why blaming frequency as the be all end all is foolish.

Reality is changed by these lens, and brain is forced to deal with light that is more noise and less signal.

This is how diseases begin with polarized light.
All nnEMF is polarized.
What happens if this is all the light you live on?

Can you make setonin, melatonin, melanin, dopamine or thyroid horomones if all the L- amino building blocks are destroyed by polarized blue light exposure?

Nope.

You become unteachable.

Your performance crashes.

You become a zoo human.

Why?

Polarized blue light destroys dopamine, melanin, and T3 and T4 hormones.  Without T3 neurons in mammals cannot operate.

That is MKULTRA in a nutshell.