Neuromodulating hormones have been turned into the transmitters, to hide bioelectricity and biophotonics behind the deceiving veneer of “molecular communication”!
The signals are not transmitted by them, this is the job of the action potentials, ion pumps, “synaptic wifi” and biophotons (produced by the mitochondria) no need to jump onto the infamous chemical-thinking bandwagon! We Are Lit- with biophotons!
Wrong concepts are believed because of the results that seemingly confirm them!
The magic works: We believe chemical signals transmission in our brain for thoughts and emotions, because chemicals have an effect on them. The causality is just assumed, because no-one can see those tiny receptors for the alleged neurotransmitters (which are just hormones).
An example of an intricate deception from “gene sequencing”!
In gene sequencing for example, there are 4 differently tuned qdots, for different wavelengths of signals, radiating in 4 different colours of electro-chemical fluorescence. They are sprinkled onto the chromosomes for electrophoresis (the “nucleotide packs” with the 4 bases). We believed that polymerase selects terminators and finishes off random sequence copies with these. We believed this story, because those qdots light up, caused by the laser light. The electrophoresis creates electrical alignment and movement, not strand separation. The camera registered those randomly sprinkled qdots and the A.I. / machine learning allegedly “restores” the full sequence in the end. They do this, to learn about conductivity and resistances / behaviour of the material, when excited by light.
We would have never accepted mass sequencing without the distraction of the cyphering of the information into the 4 base code. Light and RF beam-steering is their access into our body. This is why the neurotransmitter role of hormones, Virology and Genetics were invented. This is also why Neurology is such an obfuscating profession and we have memorised these wrong concepts globally, call the sheriff!
The neurotransmitter hoax is meant to obfuscate the biophotonic and bioelectric signalling in our brain, simple as that. If we knew, how easily light and RF can modulate our mind, thoughts, dreams, emotions, behaviour, the enemies of life would already be terminated!
I remember my neurology classes in the Albert-Ludwigs-University in Freiburg, Germany (this is when I started playing music, otherwise I would not have survived)! High flown “sCience”, from the ivory towers! We had a professor straight from Sandoz, Switzerland (where they made LSD) and she explained us the alleged complexity of our brain (while insisting on the fact that LSD would not create hallucinations, it would reveal what is usually unseen, unfelt). So we got served with headache material about our brain, all these excitations and inhibitions of countless receptors for “the pieces that fit”, Glutamate for excitation and GABA for inhibition- while glutamate can allegedly be anionic, cationic and zwitterionic (net neutral… lol). When there is a + form and - already, why the need for additional “inhibition” of receptors and why at all? There are ion channels and pumps that can do the job perfectly, mitochondrial biophotons or bions (they could be the “membrane proteins”!) could be transmitted and might trigger the opening of the ion channels at the postsynaptic cleft. So in order for the post-synaptic density to receive a signal to open the channels, there are no neurotransmitters necessary.
It gets really interesting, because biophoton research is finding biophotons that appear at the synapse, which could hint at bion activity (that Wilhelm Reich researched, this could be the “synaptic proteins” that have been recognised)- or simply biophotonic neural signalling (the potential vesicle form- as luminescent and motile bions- is very interesting at this point)The ion pumps are good at what they are doing, no need for (+) (-) and zwitterionic glutamate “receptors” to do that.
Whatever the exact mechanism might be- the official version is surely obfuscation deluxe, and it looked and sounded deeply archontic back then in university already… It was bewildering to see such brain melting complexity, but it must have been correct I thought, especially because of that complexity! Ladies and Gentlemen, I think this is another huge cover-up! In genetics they got the amino acids as the material for the aperiodic fantasy of “genetic code”, here we got hormones that allegedly transmit the signal, totally for the sake of covering up Bioelectricity and Biophotonics especially in this case!
Our pineal gland is directly photosensitive and synthesises low amounts of DMT daily, the only endogenous psychoactive compound that could be the candidate for the crystaline key to the floodgates of perception, giving us awe inspiring insights into the depth of this world and the realm of the aether, the very real hyperspace that Terence McKenna loves to talk about. When this compound is lacking, everything becomes grey and meaningless. Our pineal gland is therefore a very important part of our brain and has been in the focus of many cultures who realised its meaning, like the Mayas or true Gnostics (in John Lamb Lashs perspective), the ancient Egyptians and many others.
The pineal gland is a small endocrine organ critical for melatonin production and circadian rhythm regulation, with a unique structure that includes piezoelectric calcite microcrystals. Cutting-edge theories propose that these crystals enable biophotonic activity, acting as a “Aether connection / receptor array” or “bio-photon lens” to facilitate consciousness, intuition, or dream navigation (through the Electrome, which includes the consciousness aspect that the genome was only dreaming of).
Welcome to the Biodigital Convergence! Discouraged by the proclaimed genetic determinism of our diseases, we did not realise that every inherited illness is vibratory in nature, an imprint of the Electrome, that we inherit and this can be changed consciously. The powers that shall not be have plastered our sciences with lies about non-existing genomes and molecular communication. This is a paradigm to obfuscate the inner workings of our bioelectricity and biophotonic communication!
What If: The action potential triggers Mitochondria (present at the presynaptic terminal) to produce biophotons, guided by microtubule waveguides toward the cleft. Biophotons cross the cleft, rich with information about the presynaptic activity. On the postsynaptic side, mitochondria (and maybe channels specific for that) detect the biophotons, triggering ion flow and a postsynaptic potential.
Let’s go!
This is the alleged chemical lab, synthesising hundreds and thousands of key to lock type of “nEuRoTranSmitTerS”, to cover up Bioeletricity and Biophotonics
The human brain contains approximately 86 billion neurons. Each neuron has an axon, which may branch extensively, to form connections with other neurons. Each axon potentially forms thousands of synapses, leading to trillions of connections in the brain.
“Spatially distributed neuronal dendritic potentials generate amplitude-modulated waveforms, transmitted to the extracellular medium” [34]
The paper discusses astroglial-neuronal interactions and argues that calcium waves in astrocytes, synchronized with neuronal activity, contribute to these aspects. It mentions membrane potentials and calcium dynamics as key physiological components, particularly in the context of synaptic activity and information processing.
This is such a synapse, the place where the receptors allegedly reside is marked here (PSD, the post-synaptic density):
The archontic machine mind confirms my thoughts (PSD = postsynaptic density):
“On the other hand, bioelectricity could also regulate EV formation and release. P2X7R, an ATP-gated ion channel, was found in controlling EV release (Golia et al., 2023).”
Awkward chemical steps & unexplained biophotonic activity! Remember the wise words of Dr. Paul LaViolette, whose predictions came true 14 times (Einstein had only 3 correct): Every scientific book in the world is misinformation (I would say: disinformation):
Our cells send ions across gap junctions and the TEM scans of those and synapses look alike. I think the vesicles are just ordinary cargo carriers, also transporting ions (and there is other cargo in there too, but not for the signals propagation I think2) and the communcation is biophotonic and bioelectric (using the “fiber optic” axon and translucent heads of the synapse.
This is a hypothesis for now, so let’s see where this goes!
The Action Potential
This is how they explain it (take it with a grain of salt) :
The action potential is like a spark (biophotons!) traveling along a fuse (natural fiber optic cable!), where the spark is a rapid change in electrical charge across the membrane.
“Local” Ion Movement:
At rest, the inside of the axon is negatively charged (-70 mV) due to more sodium (Na+) outside and potassium (K+) inside.
When a stimulus triggers the action potential at one point (e.g., the axon hillock), voltage-gated sodium channels open, and Na+ ions rush into that small section of the axon. This makes the inside temporarily positive (depolarization, ~+30 mV).
Wave-Like Propagation:
The influx of Na+ in one section creates a local change in voltage that spreads to the adjacent section of the axon (and there it would cause a release of chemicals to continue the signal? This makes no sense to me…) due to the flow of electric current (like a ripple in water). I see that (and the biophotonic spark…).
This voltage change causes nearby voltage-gated sodium channels to open, triggering Na+ influx in the next section, and so on. The action potential thus “moves” down the axon as a wave of depolarization.
Behind the wave, potassium channels open, K+ ions exit to restore the negative charge (repolarization), and the membrane resets.
Analogy:
Picture a stadium wave: people (ions) stand up and sit down locally, but the wave of movement travels around the stadium.
Myelinated Axons (Saltatory Conduction):
In myelinated axons, the “wave” jumps between gaps in the myelin sheath (Nodes of Ranvier), like skipping stones across a pond. At each node, Na+ ions enter, and the electrical change leaps to the next node, speeding up the process.
The ions still only move across the membrane at the nodes, not along the entire axon.
They call this a “chain reaction”, suggesting molecules… then there is the polymerase chain reaction in “gene” sequencing … nuclear chain reaction3 … they are mocking us by indoctrinating us with blatant lies about fundamental aspects of our existence, call the sheriff!
What if this is biophotonic communication?
Light information communication! Thoughts made of Light and Electricity! No more Chemical Brain Theory!
The axon is the fiber optic cable and the synaptic “density” (because they don’t want to admit that these are sensors) is actually translucent!
They call it spark! This is quite interesting, because the 2024 study showed biophotons, allegedly created by glutamate. What if this “spark” initiates the signal through biophotons, or the ions. So there are allegedly 2 processes happening at the same time, the synthesis of all the hundreds and thousands of neurotransmitters that need to be packed into a vesicle to move along the axon for signalling (their role must be something else) and at the same time- the action potential moves and even jumps like a “stadium wave”, which is much more efficient, plus the biophotonic capacity due to the fiber optic like nature of the axon… I think one has been used to obfuscate the other here!
Voltage Potentials are driving forces of cellular communication and bioelectricity has been deliberately obfuscated in neurology and genetics. They did this, to hide the way the modulation of our electrome works: through voltage and light directly.
I think everything is much less like Lego blocks fitting holes and much more fluent ionic and biophotonic communication, similar to the way gap junctions work!
Telestai Nexus artwork from the old world!
Hey Otto, Leave the Frogs Alone!
This is a grotesque trial to find whatever … they were also looking for the wrong kind of electricity! I am glad Hodgkin and Huxley explained the bioelectric potentials of the swapping of ions through ion channels and pumps eventually and biophotons are next: Please no more mayhem, dissection of toads…. it is Bufo Alvarius (now Incilius Alvarius) that bears the secrets of the universe in his sap (5-meo-DMT)! Acetylcholine affects our brain, it is not causing the neural transmission of signals. They concluded this false idea, because they could not find electricity / current in the form with electrons! Our bioelectricity and our biophotons are transmitting signals, while hormones and acetylcholine affect the brain, there is a massive difference! There are no lock and key processes there and the signals are rather organic, either electric or photonic, with light!
Ok. Let us continue to find out what is really going on here:
Bear in mind that all of this is happening under erratic Brownian motion on the nanoscale. a wild multitude of alleged receptors, for lock and key games and very inefficient signals propagation… resembling the tales of genomic sorrow!
A lot of receptors (by far not all of them… HUNDREDS - allegedly ;)
This is a massive load of pieces floating around everywhere, into hundreds of receptors, all while under brownian motion, erratic movements in the nanoscale- where they allegedly find their receptor hole to bind… this sounds like the fabulation of someone on acid and this is not very far fetched, when we think of the Crick, Watson, Mullis brigade, who were experts in this field!
In one “post-synaptic density”, on the surface- there are allegedly all these receptors… while ion channels are there and functioning (the ions would trigger the ACH, the ACH moves to the other side and allegedly triggers the ions… I smell horsepaste!), while biophotons have been detected at the PSD, while biophotons might be generated by the action potential, received and are likely causing the ion channel to open. And we know from Watson and Crick, how eager they were to bury the discoveries about ions by Hodgkin & Huxley 1952 (very relevant at this point):
Ion Channels are always hidden and made peripheral in the graphics!
There is a possibility for this to work with bioelectricity alone, the idea with the biophotons is intriguing though, because the specific role for them is still missing and the story of neurotransmitters makes no sense.
Look at this, a brain-killer:
This looks like a factory, basically a technical map of fabulated bio-hardware… all hail to the obfuscating complexity, for eager students to absorb and throw up! Without any questions, or you are a case for “paranoid schizophrenia” and the DSM recommends to drug you up some more, with qdots and other metamaterials. But this obfuscating post-synaptic mess, is allegedly even worse in reality, with hundreds and even thousands of receptors (for muscle control), all with unique shapes and fitting pieces…. like lego … go figure!
This one is even worse, overkill:
Again: They have forgotten to even put the ion channels here, how interesting!
They love to attribute dual functions to things, hormones from endocrinie
This is how it allegedly works:
Presynaptic Side: Voltage-gated Ca²⁺ channels open when an action potential arrives, allowing calcium ions to enter the presynaptic terminal. This triggers the release of ACh into the synaptic cleft via the vesicular transporter.
Postsynaptic Side: Nicotinic acetylcholine receptors (nAChR) are ion channels that open upon binding ACh, allowing Na⁺ and Ca²⁺ ions to enter the postsynaptic cell, leading to depolarization and cellular responses.
I rather think it works with light, this might be the missing link- bioelectricity alone is also feasible but less so! The interaction of bioelectricity and light could really be key though! Biophotons have been detected in the brain and I think they are there for signalling and regeneration(confirmed by the 2024 study), just like bioelectricity!
These are the dimensions of our (neuro) hormones!
Their sizes are generally in the range of 1–10 Å (0.1–1 nm)
The sizes of our ions:
They want to make us believe that the “neurotransmitters” / hormones are 5-9 times bigger than ions, but the ions need specific channels to leave the synapse and the “neurotransmitters” diffuse throug the presynaptic density - I call horsepaste!
One more very interesting aspect is the way that the “neurotransmitter” reuptake is described. Not only is it awkward that these particles that are less than 1 nm big can fit in a lock under erratic brownian motion, which in itself is ridicuklous!
But the neurotransmitters would also move back and transporters would take them back, while some are drifting away… So while the tiny ions need a channel, the huge “neurotransmitters” diffuse through the synapse and move back, all while shaking in nanoscale earthquakes of motion! We believed that horsepaste all of our lives!
These options make much more sense than the ridiculous conversion to hundreds of neurotransmitters, in these dimensions, with erratic brownian motion and in constant movement. Bioelectricity makes much more sense, since the signal is already vibratory (with a “spark” they say… biophotons!) when it arrives and ends vibratory as electricity, I assume that it works in the same way as gap junctions function, with a very direct bioelectric signalling and sensing on both sides, imho.
So here we have the synaptic cleft, where the ions do float out but not back in on the other side- and where hundreds and even thousands of differently shaped and very complex substances, that are fitting like legos into receptors… and psychoactive compounds would also fit in these!
See the synaptic vesicle? They say this would transport the neurotransmitters and colour it respectively, but it also transports the ions, allegedly to maintain the acidity… no color though! Mind that there are only ion channels shown in the presynaptic side and not on the other, even though they totally exist! The Golgi equips vesicles with the machinery (e.g., V-ATPase, vesicular transporters) to add ions. They explain that as a secondary step but I think that the ion transport is the primary step, clearly!
Glutamate can allegedly turn into an anionic and cationic state through PH changes and these PH changes are modulated by the ion channel activity, which would basically double the process, while the ions can already do this perfectly. I assume that the main “neurotransmitters” are really just hormones and drugs work the same way and some might change the conductivity of our synapses. A lot of ion channel activity is tiring and hence there are aftereffects.
Dopamine, Norepinephrine, Epinephrine, Serotonin and Histamine are hormones. The role as neurotransmitters is meant to hide biophotonic and bioelectric communication.
Add to that the Neurologists:
Bions emit biophotons!
Maybe the biophotons that are seen at the cleft, are bions (heat was enough in Reichs experiments… ROS produces heat, for example), the action potential could cause their formation in the mitochondria. Then it is not glutamate that lights up (as shown in biophoton research)- but bions!
Wilhelm Reich described bions as microscopic vesicles (0.1–1 μm- with modern instruments, we can surely detect them when they are even smaller) formed from the disintegration of organic or inorganic matter (e.g., grass, sand, coal) when heated (the action potential creates ROS, inflammation after all), swollen in water, or autoclaved (The Bion Experiments, 1938). He observed them under high-magnification microscopes (2000–4500x), noting pulsation, motility, and a bluish glimmer, suggesting they were transitional forms between non-living and living matter.
He claimed these particles exhibited motility, luminescence, and life-like properties.
He measured microvolt potentials in bion cultures, which is an electrogravitic field!
Regardless wether these are bions or not - biophotons are surely detected. A vesicle makes sense though, regarding the observations of them travelling along the axon, guided by microtubuli - basically a fiber optic cable… great for biophotons alone already! It is not necessary though, the way it works is like a natural fiber optic cable, much better than our recreations, just like our natural chipset, made with membrane capacitor, ion channel transistors and gap junction memristors (+”synaptic plasticity”)
The paper cites studiessuggesting biophotons in neurons may be involved in neural communication. For example, it references work showing biophotonic activity (induced by “glutamate” they say…) transmitting along neural circuits, detected via ultra-weak biophoton imaging.
Biophotons (light)- emitted for healing processes and cell-to-cell communication!
They have intentionally conditioned us with “THE Matrix” (we are not living in a simulation) to expect a mechanical future and remain depressed, helpless and meaningless, when in fact- they are using the 5g towers, 6g, HAARP and satellites to get to us, to our core, our bioelectricity, while they plastered the online world with obfuscating molecular communcation routes, for the direct transduction of RF and Light to Voltage and Voltage back to Light for monitoring- and as we can see, to hide the simplicity of neuronal communication and hence make sure that we do not realise that they can modulate us with RF and light!
Abstract (…) “We point out that there is a direct relationship between neuronal activity and the biophoton emission process in the brain. Electrical processes in the brain represent sensory information from the external world. During encoding or retrieval of information, electrical signals of neurons can be converted into synchronized biophoton signals by bioluminescent radical and non-radical processes. Therefore, information in the brain appears not only as an electrical signal, but also as a regulated biophoton signal inside neurons."
The myelin’s high refractive index could channel mitochondrial biophotons along the axon to the presynaptic terminal, enhancing their delivery to the synaptic cleft.
Biophotons and Bioelectricity, just like with gap junctions (regarding bioelectricity, ions that create voltage potentials at membranes everywhere in our body and these potentials create our biofield, our vortex of electrogravitic energy!
“Neurotransmitters” are just hormones and drugs likely work in a similar way. The idea that the ion channel communication needs to be complicated by neurotransmitters, only to turn the signal back into electricity, adds a masonic dimension to the whole endeavour I think. There are ion pumps at the synapse, they can do the job perfectly fine. Hormones have an effect on the brain, this has nothing to do with neuronal signalling though, neurotransmitters are the obfuscating element, just like the genetics in opto”genetics”. If I am wrong, let me know what you think- and we can discuss this!
Never forget: We are the chip, our body is the bio-computer!
Our Lipid Bilayer Membranes (Capacitor)
The lipid bilayer membrane acts as a capacitor by separating charges across its non-conductive hydrophobic core, storing electrical energy.
Ion Channels (Transistor)
Ion channels act as transistors by voltage gating ion flow, modulating electrical signals across the lipid bilayer membrane.
Gap Junctions (Memristor) + Synaptic Plasticity (Memristor)
Gap junctions act as memristors by modulating conductance based on prior electrical activity, enabling memory-like behavior in intercellular communication.
Synaptic plasticity acts like a memristor by adjusting synaptic strength based on prior activity, enabling memory and learning in neural networks.
“Molecular Communication” is used as a trojan horse, to obfuscate the direct steering of our Electrome through bioelectricity. The Electrome is everything the non-existing genome could never be!
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They are constantly looking for ways to sneak toxic substances into our body, to get clearer tags, through the voltage fluorescence of all the coated nanodust (graphene, aluminium, titanium dioxide qdots etc…).
Aluminium nanoparticles aid with the plasmonic coupling, intensifying the light signal (our thoughts!!!) by 10x-1000x4
The mesogenic fibers from graphene help with that and lanthanides!
(There are no demons created here, they put that in the published literature so we recite it and sound mad).
Plasmonic coupling also makes the graphene qdots light signals stronger, for example, it is a supportive interaction! Near Infrared and Infrared are perfect to get good precision and tissue penetration, without too much scattering.
Biophoton research has been covered up through molecular communication and orgone / bioelectricity research has been obfuscated through the genome !
We are being lied to (through the published literature), they have dusted us with coated graphene (qdots, the WBAN “electrodes” and biosensors), which is all over and inside our cells and this dust lights up when we think, because our bioelectricity, our voltage, is turned to light, which is great for monitoring. Every cell has ion channels, where the charged ions swap places and the pattern of voltage potentials inside and outside of the cell, makes up the bioelectric signalling for our Electrome, which is everything the non - existing genome was invented for, to cover it up. They are lying on purpose, since the inception of Virology- because the implications of cracking the bioelectric code mean that you can grow a functional eye on a frogs butt, with the right voltage gradient
“genetically modified HORSEPASTE!”
They cannot admit that viruses are actually (graphene) qdots, that we are so saturated that light and RF alone is sufficient for enough voltage, to hit with 3 neuron precision (300 micrometer), with 5g beam-steering (more than one tower create a pointed signal together).
“Synthetic Molecular Communication”
This is counter intelligence par excellence! We find stuff in the blood, they explain it wrong- hence we end up sounding crazy, talking about nanobots in our blood… when they have deliberately prepared this as a trap, so that no one listens to us. There is brownian motion in the micro scale, in fluids / hydrogels - electrogravitics influence everything, so it looks like as if those nanoparticles are being steered. This way no one noticed that tons of qdots are nucleating to our membranes, sucked into the cells via endocytosis or clump together and form mesogenic “clumps” (not chips… they did this on purpose).
“Protein Sequencing” is a similar scam to “gene sequencing”, fragments are compared to known ones… where have I heard this before? So we are not built in the way they proclaim. Surely, the sum of elements in the composition of proteins might be measurable but the form giving element is not a lego assembly of molecules!
We are Electric!
"The greatest triumphs of propaganda have been accomplished, not by doing something, but by refraining from doing. Great is truth, but still greater, from a practical point of view, is silence about truth."
Fields, co-author with Levin on papers exploring cognition in biological systems , Frontiers in Computational Neuroscience, 2022), argues that hormones participate in information-processing networks that exhibit competency or agency. He suggests that hormones, by modulating cellular behavior in context-dependent ways, contribute to a system’s ability to navigate “problem spaces.”
In What is Life? How Chemistry Becomes Biology (2012), Pross argues that life emerges from dynamic chemical systems with “dynamic kinetic stability” (DKS). Hormones, as signaling molecules in self-sustaining networks (e.g., endocrine feedback loops), could be seen as contributing to life-like properties by maintaining systemic stability and adaptability.
I think the vesicles are for “Intracellular trafficking”, a process by which cells transport proteins, lipids, and organelles, within themselves- they also take care that the environment is right and this can modulate the signal of course, but they are not directly engaged in making electric and photonic communication chemical! It involves the movement of vesicles and other cargo along cytoskeletal tracks (e.g., microtubules, actin filaments) using motor proteins (e.g., kinesin, dynein). This process ensures proper distribution to organelles like the Golgi, endoplasmic reticulum, lysosomes, or the plasma membrane, and is critical for functions like secretion, signaling, and waste management.
Asking the archontic madchine mind (never blindly trust responses, without maintenance mode and tricks it won’t give us good answers about sensitive issues): Could plasmonic coupling of qdots aid biophoton intensity ?
Yes, plasmonic coupling of quantum dots (QDs) can enhance biophoton intensity. Here's a concise explanation:
Plasmonic coupling involves the interaction between the localized surface plasmon resonances (LSPRs) of metallic nanoparticles and the excitonic states of quantum dots. When QDs are placed near plasmonic nanostructures (e.g., gold or silver nanoparticles), the strong electromagnetic fields generated by the plasmons can enhance the excitation and emission processes of the QDs. This leads to increased biophoton emission intensity through several mechanisms:
Enhanced Local Electromagnetic Fields: Plasmons create intense, localized electromagnetic fields that increase the excitation rate of QDs, boosting their fluorescence or bioluminescence intensity.
Purcell Effect: The plasmonic nanostructures modify the local density of optical states, increasing the radiative decay rate of QDs, which enhances photon emission efficiency.
Energy Transfer: Förster resonance energy transfer (FRET) or plasmon-enhanced energy transfer between QDs and nearby molecules can amplify biophoton signals.
Spectral Overlap: When the plasmon resonance wavelength overlaps with the absorption or emission spectra of the QDs, the coupling is maximized, leading to significant intensity enhancements.
Studies, such as those reviewed in Nano Letters and Advanced Materials, have shown that plasmonic-QD hybrid systems can achieve fluorescence enhancements of 10–1000 times, depending on factors like the distance between the QD and the plasmonic nanoparticle (optimal at ~5–20 nm), the spectral overlap, and the geometry of the nanostructures.
Thank you for bringing this all into light no pun intended. The beauty of our being made simple rather than the complex machine that they have built i to our minds. I resonate with what you are presenting here :)
Thank you for bringing this all into light no pun intended. The beauty of our being made simple rather than the complex machine that they have built i to our minds. I resonate with what you are presenting here :)
They hide most everything in obfuscatory ways, indeed. If We're working with the wrong material, They can keep Us in Their bubble.
Thanks for offering one peek at what They try to keep from Us!