Quantum biology

The mind is made up of trillions of cells. The complexity of such an organ that creates holograms of illusion to make the person believe the universe is external to you and is physical. To break free of that illusion (Maya), you have to develop a new understanding of yourself and a framework in which to comprehend the universe that you are the creator of. That is correct. You create what you are seeing, within your mind. The mechanisms behind the veil and how I broke the illusion is what I want to share in this journey that we call life. 

We have to understand some fundamentals in order to understand how the mind creates images within the confines of the cranium and yet when we look the world around us is very large and we cannot possibly be having all of that information within us can we? Yes we can. If you read my physics of life page and the SUSY inversion model then you can understand the relationship between the Planck length (smallest thing) and the distance that light has travelled after 13.8 billion years. It is an inverted symmetry relationship. 

To begin with we see light. Light is not the fastest thing in the universe. If light was the fastest thing in the universe the universe would not be expanding and getting further away from us as it is still expanding from the beginning. We can contemplate time through the speed of light. So faster than light travel gives you a negative time. This means you can see into the future before it actually happens. This is how time travel is relevant to human beings.

The physics of time is connected to the physics of the mind. When an atom undergoes a radioactive decay event based on its binding kinetics and its half-life the time element of the unstable atom is the inverse of its half-life. For example 23 ms is approximately 43 years. So if an atom decays for a short period of time and you experience this you can witness photographic information of events in your future. I know this sound strange.

Consider the light that you see. It has no mass and no charge. Therefore, it travels at the speed of light within the features of the mind of the individual experiencing that vision. Whereabouts is this light. Is it experienced at the retina? Consider the perception of three dimensions and the forth time. I would like to discuss the physics of light within the mind and the creation of those dimensions including time.

You could say somewhat that this is a reductionist model. However, what measurement device do I have in order to understand the inner working of my mind. The answer is my mind itself and the logical approach to understand the physics happening within biology and my perception, awareness and my own personal experiences that are unusual and at times you could say perplexing. It is only using logic that a framework of understanding light within the mind that can be aligned to the experience of being human, having conscious awareness of self and the mechanistic features of biology that are responsible for creating that experience.

Our eye anatomy. We have inverted retina. The rods and cones are on the inside of the eye. The reason for this is to understand that the majority of light observed originates from within the mind. 

We see our dreams at night with our eyes closed. The light within dreams originates from within the mind itself and there is now clear evidence for the origin of this light within the mind from single atoms that are releasing light in the radioactive decay process that is responsible for making the atoms stable and have a balanced structure. SUSY inversion model provides context of what atomic stability looks like where the number of protons, electron, neutrons, and positrons are all equal.

Atoms need to be in a stable state in order to create a stable mind. If you do not get to sleep for several days then your mind does something. It does radioactive decay of single atoms to release the imbalance within the atoms. This is the underlying physics of mental illness. Seeing things that no one else can. Hearing things that no one else can. You tuning into a different time and a different place from everyone else because the process of atomic decay is a turning folk. It is how your mind connects you to the universe. Consider the time reversal symmetry and time dilation associated with atomic decay events. Each atomic isotope having a different half-life and therefore frequency in which it operates. You tune in to the universe using the radio frequencies of the atomic minerals within your mind. So where are they? And how are they associated with the light we see and the formation of memory?

The construction of our three dimensions x, y, z comes from the features of light itself. Consider the right hand rule of electromagnetism. The interaction between an electric field and a magnetic field which is what light is. Whereabouts do these field interact with one another. This comes the trick part. You have to look at each individual component without time, without change and without space and mass. To do this you can use only a logical framework of light itself. As light has no mass and no charge. We know that the electromagnetic force is light within atoms. So my approach has been to use Planck epoch distances within atoms and understanding the electromagnetic fields within the atoms themselves. As I have already outlined in my SUSY inversion model, I use inverted symmetry to understand positioning of positron and electron pairs within atoms to explain features of hydrogen's ability to quantum tunnel. The inverted symmetry model at Planck scale provides the singularity framework in which to empirically position positron and electron pairs within atoms through a point light source framework for each positron or electron within the S orbital structure to produce the P orbital structures. This approach means locality and speed are known at the point where quantum tunnelling can occur. No measurement is required because of the features of the locality where the singularity physics model is applicable with respect to human mind biochemistry.

The locality is within the aromatic ring of the neurotransmitter, where there is only room enough for one atom. What are the features of this unique environment that make this suitable as the storage system for memory in the mind and how does this link to short term and long term memory, the biochemistry of neurotransmitters and the functional role of hydrogen in biology and its linkage to the light we see.

To begin with we must understand the photo-electric effect in the SUSY inversion model with the inclusion of positrons within the S orbital structures of atoms. It is proposed that it is the motion of positron and electron pairs that is responsible for generating the wavelengths of light that occur in the visible region of the electromagnetic spectrum. We can understand these transitions and the colours they produce as red, aqua, blue and violet. The cones within the eye perceive red, green and blue. By absorbing red and blue the two ends of the spectrum only green remains. It appears the orbital transitions of hydrogen play a functional role in the creation of visible wavelengths of light within the subconscious mind. The mind outside of neurons. This is part of the mind that has not readily been considered by neurologists and this is the area of focus that I wish to provide a logical basis for in terms of vision in a 3D environment and within a temporal and spatial reality that we perceive within the mind. This will be a detailed mechanistic aspect of inner vision and its operation based on physics happening within single atoms. This monoatomic single atom memory system that I am proposing is operating using hydrogen and the features of the model that are coherent with memory and biological understanding of our experience of ourselves.

As outlined in the physics of life, everything originated from 16 electrons per atom of helium at the ground state in a Bose Einstein condensate. If you can wrap your head around that one then lets explore memory. We will zoom down to the scale of a single atom housed in the aromatic ring of dopamine neurotransmitter. For the understanding of the mechanism you must understand that the neurotransmitter is made from an amino acid tyrosine or phenylalanine. The hydroxylation and decarboxylation is necessary for producing the functional role of the neurotransmitter as an atomic machine producing memory from light, hydrogen and through coordination with water and other neurotransmitters outside of the neuron in the extracellular matrix where is does the following remarkable thing and that is to generate atomic isotopes.

By removing the carboxylic acid group the amines function can change from the charge relay aspect of the planar bond formed in the peptide bond to a functional role in hydrogen exchange with water depending on pH of a local environment. The pKa of the dopamine amine is such that it is partly protonated and partly unprotonated. This exchange of proton with water provides a driving force that allows NH3+ and the n=3 Paschen lines wavelengths of 820.4, 954.6, 1005, 1094, 1282, and 1875 nm corresponding to infrared wavelengths of electromagnetism.  

Improvements in cognitive performance have been seen with the treatment of infrared light (NIR 800-900 nm). Infrared light corresponds to 820.4 nm for Paschen line electron transition infinity -> 3. This improvement is proposed to be related to the n=3 NH3+ transition in the process of quantum tunnelling in the dopamine molecule where hydrogen is added into the single atom monoatomic system allowing the generation of an isotope. The Balmer line electron transitions correspond to visible wavelengths of light from n=2, 3->2 red light, and 5->2 blue light. Both red and blue adsorption spectra are present in the retinal cones. Is there a correlation between electron transitions and retina cone mediated colour vision? My hypothesis suggests that this is indeed the means by which colour vision developed within the subconscious mind and the evolutionary selective pressure placed on the eye for the orientations of the rods and cones as well as the adaptation to detect specific wavelengths of light. Providing a basis of evolution of vision in its current form enables one to consider physics to apply the adaptive pressure on a local environment to select for the correct chemistry that leads to the adaptation of the biology to suit the purpose of the selection pressure on a given localised environment within the organism to generate the functional outcome observed.

 The decarboxylation is one aspect of the functional role the amine plays in delivering hydrogen through quantum tunnelling into the aromatic ring of the neurotransmitter (dopamine) in order to provide a memory based atomic clock system. The isotopes are unstable and they are returned back into a stable state when tunnelling returns the flow of light out of the atom and connects back to the hydrogen amine functionality but in the reverse of the initial process. This delivers the stored memory back into water structure surrounding the neurotransmitter. This connection between water (H3O+ and OH-), pH, protonation of the amine NH2 <-> NH3+ gives a connection between the high water content of the mind 85% and the functional role hydrogen has in generating visual information via Balmer line electron transitions. 

The MAOI (monoamine oxidase inhibitors) play a role in turning off the NH3+ hydrogen quantum tunnel delivery system for memory formation. It is known that MAOIs affect visual information obtained within and the relationship between the NH3+ hydrogen delivery system and the amine functional role and its oxidation provides a context for the visual disturbances induced by MAOIs. This further supports this model for vision within and the hydrogen system of amines and quantum tunnelling in close proximity to the aromatic ring of the neurotransmitter. This is also seen in serotonin. Another clue is the SSRIs where the inhibition of the uptake of the neurotransmitter by the receptor can increase increase health benefits in relation to wellbeing. This provides context to the functional role of the neurotransmitter external to the neuron firing in the generation of the light through the quantum tunnelling of hydrogen from the amine. I hope you are starting to understand the functional role of the neurotransmitters outside the neuron in the extracellular space. 

If you also consider the PUFAs poly unsaturated fatty acids present in the neuron plasma membrane and the idea of cis / trans isomerization in retinal in the rods and cones to be able to convert photon signals into electrical signals. Then, this concept can be applied to the functional role of the plasma membrane PUFAs in neurons which can absorb photons produced from the hydrogen monoatomic system in neurotransmitters outside of the neurons. As photons of visible light are longer than the neuron axon then light can pass through without interference. This conceptual model provides the basis for understanding how a three dimensional environment could be constructed within the mind, where the neurotransmitters generate the light absorbed by the neurons themselves. The light is generated through the process of isotope generation and the isotope decay process releases that light in a time reversal symmetry corresponding to the atomic half-life of that isotope. 

This is where time comes into the picture as well as the three dimensional environment. Consider the single atom housed in the s orbital spheres and the hexagon geometry of the aromatic ring of the neurotransmitter. Does the 3D environment come from the 6 sides of the hexagon itself. The the single atom in the centre of the hexagon has around it pi electrons. The hydrogen delivered via the amine functionality above the ring and the geometry of the electron and positron pairs in hydrogen in this unique location allowing quantum tunnelling. As the Balmer line transitions correspond to visible light does this enable a connection between 3D and time within the aromatic ring where the isotope formed and its half-life provides a decay time that corresponds to the release of light from within the the aromatic ring during the decay process and thereby providing a time reversal symmetry that is like Déjà vu where you experience both the inflow and outflow of hydrogen in the formation of the isotope and the decay of the isotope where the time reversal symmetry aspects of atomic decay provide the mechanism whereby Déjà vu is experienced. The fact that the atomic memory system aligns with human experience provides a strong correlation to our inner light based reality.

The idea that dreams are released as photons of light in the atomic decay process where sleeping restores atomic balance in the memory function of atoms themselves provides a strong correlation to the functional role of the physics of isotopes in the formation of memories and in memory recall and the role in sleep and the aspects related to lack of sleep and atomic decay and the experience one has when seeing things that no one else can see because of atomic decay processes and the time reversal symmetry aspects related to a different reality perceived from Balmer line transitions of visible wavelengths of light to Lyman lines and seeing a golden sphere of light. This tunnel of light seen in near death experiences corresponding to Lyman vision lines and the UV catastrophe were higher forms of energy are released in atomic decay.

I relate this to the spiritual practices of times gone by where visions within are connected to the functional role of alpha particle emission from the atomic systems within the mind that are part of the natural memory system. Again, further evidence to support this thinking comes from my own personal experience and the product that I make that helps to unlock the trauma that is housed in the atomic rings of neurotransmitters. The physics of the breakdown of the aromatic rings containing iron using photo-Fenton chemistry seen in the product OH BEE HAVE empowering healing means that past trauma can be released and this is able to be healed and if we consider the intergenerational repeating patterns of trauma in families, then we can understand how the atomic memory system can get encoded into a persons behaviour. This behavioural process creates an external environment that can be learnt and passed onto the next generation. 

The role of atomics in memory storage and its role in the function of the neurotransmitter from short term memory (water based) influx into the amine (NH3+) and the quantum tunnelling feature to generate the isotope. The transition to long term memory and neurological processes may be related to the breakdown of the neurotransmitter through the photo-Fenton chemistry process that is involved in the hydroxylation of the aromatic ring. Eventually, after sufficient hydroxylation, the ring is broken open and glyoxal or methylglyoxal is formed as well as dihydroxyacetone. These small molecules are highly reactive and may be involved in producing new neuronal connections and the dynamic interplay of axon interactions. These small molecules can be converted into lactate by the glyoxylase pathway and this connects to neuron energy generation and ATP production which connects to an internal energy system for the neuron and the normal biochemical processes at play in learning.

Features of this model and memory formation go from light, photons, hydrogen and atomic isotopes and the connection to water and its structure. One thing I have not outlined is the origin of water in the first instance and that is not from what we are drinking but the water within the cell itself coming from the harvesting of hydrogen through biochemistry of glycolysis, the Krebs cycle and the electron transport chain (ETC). The hydrogen gradient in the mitochondria being responsible for the formation of ATP and water. It is the hydrogen in the water within the cell that is needed for the amine protonation and the linkage between the food we eat and biochemical energy with the memory formation process and the role of hydrogen that is pertinent to understanding that deuterium cannot undergo quantum tunnelling. As others have outlined the functional role of the biochemistry of the mitochondria is the use only the form of hydrogen that can quantum tunnel, H( 1/1). It is therefore important to recognize the role and relationship between the food we eat and our mental health and wellbeing. Not only is the water generated in the cells needs to be quantum tunnelling proficient but the aspects of the mind model clearly shows the isotope aspects of mind biology and the physics of the mind makes use of H 1/1 in an inverted symmetry model whereby the positron and electron pairs in hydrogen are able to make the hydrogen atom have no mass and no charge making it competent for quantum tunnelling. This clearly highlights why the geometry of deuterium is unable to perform tunnelling and thus makes it unsuitable to support good mental function and memory generation.

Here the plug. The functional benefits of OH BEE HAVE empowering healing are your guessed it enhanced mental wellbeing by supporting the physics of single atom systems which occur naturally within the aromatic rings of antioxidants present within the phenolics of Manuka honey. It is the monoatomic systems that are responsible for their potential benefits to brain health and there nootropic properties. Understanding that comes from both using the product and having had a number of years to develop the scientific logic based model to frame the single atom system that resides inside the aromatic ring of the phenolics and see the relationship to our own neurotransmitters and their functioning in the biochemistry of the human mind. The atomic light based storage system has therefore been discovered and the electromagnetic force within atoms provides the basis for memory storage and recall. The model does not outline what memories are stored but merely provides a basis for atomic memory and the features of physics that correlate to the biology of the human mind. A doorway has been opened and if you are willing to cross the threshold from measurement to logic then you can enter. Otherwise you are stuck in the past as the time required to gather the information from the measurement and process the details into a coherent story means you are always living in the past. Only when you let go and understand the balance that happens during sleep to restore health and wellness can you begin to explore the functional role of atomics within the mind. 

The time lock we appear to be in is a feature of the isotopes the mind uses and the infrared energy used to quantum tunnel versus the instability of the isotope and its light release process that is the time taken to return the atom to its stable state and when it is ready to receive the next hydrogen atom from the amine. This time loop is a function of the on and off rates and pH in the local environment and will correlate to perception and cognitive speed. This may be associated with brain wave levels providing information to the local neurons via the PUFA mediated cis /trans switches and enable the localised 3D perception within the realm of the mind. The inverse square law and SUSY inversion model provides a context of the smallest thing being opposite the largest in the inverted retina and the scales that the electromagnetic spectrum operate at the visible region in the nm scale appears to be somewhat positioned between the extremes of ELF and gamma frequencies. The use of light and isotopes and the features of the biology from the perspective of hydrogen generate a beautiful unity of the creation of the universe as an inner reflection of an external reality. 

I hope that sheds some light on the inner light show and a potential way to support people's own personal mental health journey to be reconciled with your biological anatomy in a functional mechanistic model that enables one to understand on the functional role light has within the subconscious mind in the creation of the observed hologram you perceive as the external universe.