Full Breakdown of the Qdots and Mesogenic Fibers: No Robots in Sight!
Our Biology & Mesogens become the Bot, through Bioelectricity! Qdots are self blinking rectennas, from 5g to voltage and voltage fluorescent tags, not robots!
Greetings! This article shall shed some more light onto the peculiar nature of those “q” - dots (regardless of the odd name- they are something fundamental to the deceit of virology and genetics, in order to read and write biological signals). Moreover, we will look at the nature of those mesogenic fibers we are finding in the blood and in our environment, which seem to be growing under electromagnetic radiation, while being made of liquid crystal. Let’s go!
Qdots are Key to the Triggering of Neurons with Light or 5g signals- and to "read & write thoughts" (among countless other biological functions, since bioelectricity and therewith voltage, is the language of our cells)!
For centuries we have been lied to about the hijacking of viruses and delayed effects of tick bites, HIV and so much more- to cover up the damages of this universal deception!
They are self blinking rectenna - tags and central to the interfacing of our bioelectricity, which includes action potentials of neurons as much as the signalling for the regeneration of our epithelium (from 5g to voltage and voltage to infrared light), No robots necessary! This was a psyop- there are only Bio-Bots (under synthetic fusions) and this will be explained in the second part of the article! Never forget: Your Cells are the Chip!
The amino acids and their allegedly “infinitely complex arrangements in chains” (another fictional sequencing rabbit hole…) are not the basis of our biological functioning or decision making at all: Bioelectricity is! We have been made to believe that everything is arranged in a coded form like our language, aperiodic molecular encoding. In reality, this has been a deliberate distraction from the progressive orchestration of our biology through voltage signals, and no one said a word! “It’s in our DNA” they said… this was a monumental lie!
They are leveraging our biological “hardware” (our cells are memristors and transistors, processor and memory in one, with synaptic plasticity), in conjunction with nanoscale metals and other materials, for the self assembly of mesogenic structures for signals propagation through our cellular architecture. Our cells generate a vortex of energy, our biofield!
Soap & detergents… This is why the LNPs were advertised as little “soap bubbles” - graphene qdots are liquid crystals after all. They are very sneaky with their wording at Moderna & Pfizer (and long before that time), always hiding their real intentions, namely bio imaging and bioelectric orchestration!
Boolean logic computation, memristor, transistor, depolarisation, voltage gated ion channels : This is not happening on synthetic / metallic recreations in our bodies: OUR own CELLS are THE CHIP!
Deliberate misattributions // The rendering of those who recite them as insane // …with respective entries into the DSM for “Psychology”. Philanthropatic Deception Everywhere!
The Invisible Landscape
Graphene qdots have excellent properties. They are the rectenna to turn 5g signals that are 300 micrometers precise (with beam-steering) into voltage, Bioelectricity!
When they talk about “energy storage” and “energy harvesting”, they keep it unclear, so we conclude that it must be like a vampires bite, sucking our life blood. In reality they mean the conversion of RF to voltage, which guides our bioelectricity through voltage gradients resolved in the space of our cellular architecture and over time. This way they can trigger emotions, memories, behaviours and virtually all biological functions, while we have been distracted with the non-existent genome, like a carrot on a stick, promising the answers but giving none!
The qdot with its naturally formed protein corona is the (Corona) Virus! - The protein corona forms naturally in our body, when the cationic nanoparticle fuses with elements (proteins etc.) in the blood, hence the name “corona virus”. The corona satellites are also the first spy satellites ever used…
Nanoscale “magic” (rather dementia)
The space that is invisible to the naked eye is filled with artificial compounds that have been labeled viruses or spike proteins, with matching toxicity profiles. “mRNA” is the trojan horse story, totally made up and meant to hide the interfacing of our bioelectricity. “Nanobot” has been a misleading misnomer, because it drives our attention away from the “programmability” of mesogenic crystals, namely liquid crystals and the possibility to steer our very own cells through graphene qdot - transducers (simply the graphene dust with coating), that nucleate to the cells membrane or become part of these mesogenic fibers.
“For every disease that we don’t have vaccines, we will try “mRNA”. We just need to mess around. There’s a lot of lipid nanoparticles, and some are very self-assembling.” Bill Gates
mRNA = Nanoparticle with a fake story to deploy them = Voltage Gradient Pulsing (from RF or LED / NIR / IR to Voltage) for short term goals like depolarisations of neurons and pattern pulsing of emotional states, for example. And bioelectric patterning serves long term goals like regeneration or the modification of our sexual orientation … all within the spectrum of unsupervised possibilities of the powers that shall not be. Decentralise control! Transparency for us? Then create transparency for everybody! Problem solved.
…They are hacking us and no one said a word how… don’t expect their talk about the tele-health revolution to have any substance in regards to actual health for us… they are lying about the cytotoxicity of it all, about its nature and want to keep the control by all means.
They needed to find a way to explain the protein corona and because it is forming around all the artificial nanoparticles in our body, they just took the elemental composition of that protein corona with a graphene qdot and invented the spike protein in that way.
So what they are doing with over unity energy generation, is hidden in “nuclear” programs or the “UFOs” are allegedly from Aliens, while the interfacing tech is blamed on nanobots and sometimes aliens too. This is a great way to render everyone insane that investigates and a perfect shielding in that way!
The world does not operate like a computer, there is cognition all the way down and up and every element of nature interacts in reaction and diffusion, according to subquantum kinetics. We can grasp that intuitively, or through experimental evidence, as Michael Levin has done (for Microbiology).
The world is not a machine, hence we cannot mechanically predict the outcome of changes to this system with consciousness on every level. There is a dimension of form, where even our memories are stored. There is no representation of that information here in 3D, according to Michael Levin. He proved it in his experiments, where decapitated flatworms regrew entire brains, with old memories restored- no “genOme” involved!
Dr. Robert Malone proclaimed to have found the way to get “mRNA” into the cell, which is the endocytosis process and these stealthy nanoparticles from graphene are (first) recognised as part of our own body (the inflammation shows us that they cannot fool our body for good) and thus they are taken in and enlighten our voltage language for those Philanthropaths who lie by omission.
You see, the cationic charge of these tiny allotropes1 of carbon (graphene)with coating, leads to a massive protein corona crown, almost the entire thing is then made with proteins, hence the name spike protein. Also, because of the spiky deformations of our cells, from all that graphene and protein corona spiking!
The qdots are the rectennas, there is no need for additional gear but the hydrogels help to bind and the mesogen fibers suck some up. There is clumping and we are witnessing the creation of novel tissues and other bioelectric experimentation on humanity everywhere. The A.I. learns from all these experiments with their rat- bats of the world.
Graphene Quantum Dots
GQDs offer unparalleled potential to manipulate ion channels via light-to-voltage conversion, advancing Levin’s bioelectricity research in morphogenesis, regeneration, cancer, and synthetic biology. Their rectenna-like behavior, tunable bandgap, functionalization, conductivity, photoluminescence, electrostatic interactions, photothermal effects, and quantum confinement enable precise Vmem control.
You can see the qdots in red sprinkles on the cell! This is how they are doing it, this is what we are seeing in microscopy and this is what they are covering up!
This is how the interfacing is being presented (little chips flowing through our bloodstream… this is not at all what is going on and yet there are many hardcore believers out there):
A COINTEL Narration to distract from the hijacking of our cellular architecture as the chip (memristor and transistor function of our agentic cells, their bioelectricity, voltage gradient communication)
Here is an example of the transformation of blood, with countless qdots and a type of polymeric web, roulleaux formation of the red blood cells and mesogenic clumps! You can see the nanoparticles under brownian motion, the erratic, electrogravitically reinforced motion.
This is how it looks like in reality:
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Notice the polymeric webbing in the background. Dr. Ana about the nanoparticles under brownian motion (audio). She sees them as robots (fair enough, she does that in good faith). It is interesting that she notices, how they become part of the mesogenic assembly, while I think that construction by nanobots is a misconception. I rather see the self assembly as an attractor for the erratic brownian motion and particles that then become part of the assembly through electro-gravitical attraction and properties of the mesogenic structures directly. I personally think the nanobot story is a cointel narrative, to distract from the fact that this material can hijack our bioelectric communication, our Electrome.Once you understand how bioelectricity works, and how easily our voltage language can be hacked, that the LNP were these graphene rectennas, billions of them- not nanobots, then you grasp the magnitude of the deceit, while they are already under our skin, under false pretext! Call the Sheriff!
Dr Ana says that these erratic particles would become part of the polymer construction, so imho- this is the assembly of liquid crystal material, conditioned to certain outcomes, according to Michael Levins findings about voltage gradient pulsations that change the behaviour of systems in nature, that have agency all the way down and all the way up, hence it is possible to create these self assembling fibers. They serve as dialectic antennas and they sucks up many qdots from graphene, which turn RF into Voltage, for example (also lanthanides and other metals, aluminium etc.).
Nanoparticles in erratic, brownian motion- do not construct the mesogens, but charge and functional groups, chemistry etc. can very well drive this. The swiss research team is claiming an electrospun nature of the fibers.
The narration around nanobots, especially in cancer medicine- is a red herring to distract us from the power of voltage gradient pulsations that can bring cancerous cells back to normal functioning, for example. The stories about protein folding are also false.
GQD = Graphene Quantum Dot (the word quantum stands for quantum confinement effects due to the size and properties of the material)
Surveillance under the Skin + Bioelectric Orchestration from External Sources!
1: Rectenna-Like Light-to-Voltage Conversion for Ion Channel Modulation (our bioelectricity).
GQDs function as nanoscale rectennas, absorbing electromagnetic radiation (UV, visible, or RF, including 5G frequencies at 3.5–28 GHz) to generate localized electric potentials that modulate ion channels. Their carbon lattice and π-electron system enable efficient light absorption, converting photons into voltage via electron excitation. This voltage alters the electric field across cell membranes, influencing voltage-gated ion channels such as sodium (Na⁺), potassium (K⁺), or calcium (Ca²⁺) channels.
2: Tunable Bandgap for Tailored Voltage Delivery
GQDs’ size-dependent bandgap (0–6 eV) allows precise tuning of light absorption, optimizing voltage output for specific ion channels. Smaller GQDs (<5 nm) absorb UV light, generating higher-energy voltages, while larger GQDs target visible or near-infrared spectra, producing lower-energy pulses suitable for cellular signaling. (I think they are lying and there are a lot of bigger qdots in use than they admit to…)
3: Surface Functionalization for Targeted Ion Channel Control
GQDs’ high surface area enables functionalization with biomolecules to target specific ion channels or gap junctions, enhancing voltage delivery precision. For instance, anti-connexin-functionalized GQDs can bind gap junction proteins, modulating intercellular bioelectric communication, a key focus of Levin’s collective intelligence model.
4: High Conductivity for Efficient Voltage Transmission
GQDs’ graphene-like structure, with delocalized π-electrons, ensures high electrical conductivity, enabling efficient transmission of light-generated voltages to ion channels. This conductivity creates stable electric fields near cell membranes, shifting ion channel states.
5: Photoluminescence for Real-Time Bioelectric Monitoring
GQDs’ tunable photoluminescence (PL) enables simultaneous voltage generation and real-time monitoring of bioelectric signals. PL intensity correlates with local electric fields, allowing visualization of Vmem changes, similar to Levin’s use of voltage-sensitive dyes in tadpole embryos.
6: Electrostatic Interactions for Membrane Polarization
GQDs’ surface charge (positive or negative) influences membrane electrostatics, modulating ion channel activity. Negatively charged GQDs polarize membranes, lowering VGCC activation thresholds to enhance Ca²⁺ influx, critical for Levin’s differentiation studies. Most qdots in use are cationic, positively charged- and attract the negatively charged membranes of cells.
7: Photothermal Effects for Localised Voltage Amplification
GQDs can convert absorbed light into localized heat, enhancing voltage effects through photothermal mechanisms. This heat increases membrane fluidity, lowering ion channel activation energy, amplifying voltage-driven responses. In Levin’s regeneration studies, photothermal GQDs could enhance VGCC activity, accelerating Ca²⁺-driven proliferation.
8: Quantum Confinement for Enhanced Voltage Precision
GQDs’ quantum confinement effects, arising from their nanoscale size, enhance electron confinement, amplifying voltage output precision. This allows sub-millivolt control of Vmem.
These 8 special properties make it possible for Graphene Qdots to electrogravitically attract materials (cationic charge), clump them together and grow longer mesogenic fibers from “templates”, all in the framework of bioelectrical orchestration.
These little “spider silk” threads are growing in our blood, attracting the compounds for their enlargement and often we can find qdots blinking inside of their hollow inner tube. These threads have been found for decades but are now more common, especially in regards to the clotting issues of human blood in this era of ubiquitous poisoning of our environment.
The fibers can be modulated, just like all agentic “material”- life does not begin at the level of cells and Michael Levin brings forth evidence that breaks down rigid conceptions of life. Bioelectricity has an influence on it all!
Polyamides, the same proteins that we found in the rubbery clots in our vanes and arteries!
Image with visible qdots in the fiber (Image by Dr. Ana Mihalcea)
This study talks about fibers like the ones we are finding, with qdots for bioimaging, they are like fiber optic cables after all, functioning as transducers and antennas. Essential, especially for the lower frequency range of bluetooth etc.!
Some of the chemical compounds found are not registered
Most concerningly, some of the chemical compounds found are not registered in any known Safety Data Sheets, suggesting that they are new or experimental substances.
Click the Link to the Full Video about the Swiss Research Team and their Findings
These are their results: Polyamides and a great Carbon to Oxygen Ratio for Graphene. One thing is for sure, the perpetrators have surely flooded the published literature with explanations that will lead us astray. For now, we know that they are mesogens and that they somehow grow or chemically react with other elements in the blood to form longer fibers. Karl C had great success with Sodium Citrate to get them out! One thing is for sure: they are lying about “drug release”. What they mean is that when the qdots are in this “fiber optic cable” like dialectic “antenna” - then bioelectric instructions can be sent to the cells, which produce the desired drugs. When I hear them talk about electrospinning and how the materials for “drug release” are incorporated in the hollow inside of the fibers, I am drawn to conclude that what they are describing is happening inside of our body, so that the qdots become part of the fiber which makes an excellent dialectic antenna, given the amount of metals that are found inside.
Hildegard Staninger wrote her detailed work about mesogens, unaware of the fact that most narrations regarding nanotech are cyphered, meaning that they will never directly talk about the power of voltage gradients caused by the excitement of qdots (or mesogen fibers that incorporate them) in our brain. So even Staninger is confused and conflates the real concept of bioelectricity that drives our cellular architecture, like a chip- and the alleged “brain chip”. This is due to a confusion of how the interfacing truly works and this confusion has been introduced by design.
Staninger about the ordering of liquid crystal mesogen fibers (“Nano Machines for Ultimate Control of False Memories” p. 6)
The title of her book is misleading, but most of the science around the composition and behaviour of the mesogenic fibers is being described perfectly. The deliberate obfuscation of the inner workings of such interfacing leads to the false attribution of these mesogens as part of a chip (aggregates of cells can compute, our cellular architecture is the chip for the Transhumanists, they deliberately disinform us). We have 1 trillion gap junction cells available for biocomputing, which goes way beyond the limitations of our rigid mechanical possibilities that are propagated as “nanotechnology”, while no one mentions the very real biotechnology they are after, with nanoscale qdots and other elements for interfacing, do you see how they operate? Bioelectricity governs all of our biological functions and this knowledge has been hidden from us for the last 75 years. The mesogens are not computing themselves, nor are there nanorobots with A.I. consciousness. Michael Levin spoke about agency on every scale so it is not absurd to assume that electromagnetic steering can add to the structure of mesogens that might be combined with something biological (or not) …
They are cationic polymers, hence materials are attracted through a gravity well (electrogravitics). The makeup of these mesogens allows for the growth, for the enlargement of its nematic form. It is clear that these materials are being used for the transduction of RF or Light into Voltage, the language of our cells and back. Details about the self assembly are in the document (click the image). The narration about the chip is misleading though, since our cells are the transistors and memristors, with a depth of memory of up to 10 levels. Our cells have natural agency though and protein synthesis does not work with code as proclaimed, it is rather an alchemical fusion infused with the instructions from our Electrome (or forced externally).
Our perpetrators are deliberately spreading confusion around the way our biology works. We have been conditioned to believe bio-fiction about aperiodically organised DNA molecules, storing a code and that protein folding would use such code for the mechanical assembly of the proteins. In reality, it is alchemy that is providing new tissues through the self replicatory principle in nature.
She goes on describing the mesogen fibers as rod shaped organic molecules.
Here you can see one of those mesogenic fibers and countless qdots, plus RBC with material inside (likely more qdots):
Image by Ria No More Silence - There is a huge nematic liquid crystal mesogen right there! These are found everywhere and in everyone now. Tony the Nanobucket Guy found a way to get them out, that works great with sodium citrate and borax! You can see the tiny dots and materials that entered the cell and the spiked deformations of the membranes.
They can be aligned by external magnetic or electric fields, with the properties of uniaxial crystals! Voltage and Light! It is all about our Bioelectricity and a way to tag our cells with qdots that turn it into voltage fluorescence that can be monitored by our smart devices for the biodigital convergence! There is still a possibility that the “candida” story is somehow connected and that these mesogens could be fused with a bioelectrically modified mushroom, that is infecting us globally and the spraying aids this life form as food. This is a possibility but for now I think that the “cross domain bacteria” gene sequencing of this is misleading and that there are surely no genomes in these mesogens! But the idea that a mushroom could be used to cultivate these is still worth investigating! But even without that, self assembly is feasible!
These mesogens match the graphite spectrum (remember that Rosalind Franklin was working on graphite when she basically discovered graphene in 1951 and she also considered the first “virus” to be a liquid crystal… how interesting ).
Clifford Carnicom made a lot of interesting research. The sequencing of the material makes no sense, since we know that a life form cannot truly be defined by this fraudulent way of reading bioelectricity, or the interaction of qdots with the sequenced material (qdot patent).
The idea that an underlying mushroom culture could be involved is intriguing!
“Nanobots”
Deliberate confusion is being induced, through terminator like horror stories. about the alleged merging of our biology with the machine, in a way of machinisation (of course it is merging with A.I. but they want to bio-compute over our Bioelectricity, with centralised control).
It is, in fact, our bioelectricity2 they are after, to modulate every possible biological function. There is no rational need for anything else in our body that would mimic totally feasible bio-bots from our cells, by merging them with synthetic materials and by remote orchestration through our smart technology, 5g towers and more.
So “nanobots”, besides the misinterpretation of the brownian motion of qdots and other materials at the nanoscale, must be bioelectrically modulated liquid crystal “material”, just like cells! The mesogenic fibers can then incorporate other materials more easily. Even elemental matter can have a type of cognition, according to Michael Levins experiments, so they can be conditioned to perform certain jobs.
Michael Levin suggests that even simple systems, such as molecular networks or single cells, demonstrate forms of basal cognition, including learning, memory, and problem-solving, which are hallmarks of agency.
Levin proposes extending these principles to synthetic materials, such as engineered tissues or hybrid bio-synthetic systems. By programming interactions (via bioelectric voltage gradient signals), synthetic matter could exhibit agency, such as self-repair, environmental adaptation, or collective decision-making.
There you have it! This could explain the self assembling mesogenic structures we are finding in our blood! They are reprogramming nature through bioelectricity- while we have been bamboozled with the genetic cypher !
This is the way the self assembly could be programmed, so that these liquid crystals, the mesogenic fibers we are seeing in the blood, are bioelectrically orchestrated to perform certain tasks.
In synthetic systems, Levin envisions using tools like “optogenetics” (a deliberate obfuscation, it is simply light to voltage- through the rectenna function of qdots), synthetic biology, or computational modeling to design interactions. For example, synthetic cells or materials could be programmed to respond to external stimuli (light, electric fields) to achieve specific goals, such as targeted drug delivery or self-assembly.
Levin’s work challenges the view of matter as passive, proposing that agency is a fundamental property of appropriately organized systems. This has groundbreaking implications for understanding life, cognition, and the potential of engineered systems.
It is highly likely that this is the modus operandi for those that deployed these liquid crystals. Through some way of engineering, they are incorporating materials form the blood to enlarge their form, which acts as a perfect RF transducer from the bioelectricity of our body, turned to light through the graphene qdots, under plasmonic coupling by aluminium qdots, aided through a general saturation with graphene and metals, often lanthanides.
“We’re interested in creating systems, whether they’re biological or synthetic, where the matter itself has agency through programmable interactions. You can think of it as engineering the rules by which components talk to each other, so they can collectively solve problems or achieve goals, like self-assembly or adaptation.”
Michael Levin
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It is all about our Bioelectricity!
At the same time, a whole brigade of mice (as their symbol on x) is advertising Methylene Blue as a solution for the non-existent “spike protein” (these are graphene qdots, or other materials). Methylene Blue- a dye that aids with the conversion of light to voltage for our cells. Meanwhile, this “mouse brigade” conjures up a bullet proof viral sequencing fata morgana online. Sequencing is just the cyphering of bioelectric readings from the material, either from the interaction of qdots with the sample material when excited by the laser, or directly through voltage sensitive semiconductor chips.
Be careful out there! Many of the people advertising this have no idea about this bioelectric dimension. This is due to the obfuscation of Crick and Watson and later Kary Mullis.
We can communicate with all beings of Nature, through ourElectrome, our energy field!
Morphogenesis: Bioelectric signals guide the formation of anatomical structures during embryonic development, determining organ size, shape, and position.
Regeneration: Bioelectricity controls tissue regeneration, as seen in planaria and amphibians, where altered voltage patterns can induce limb or organ regrowth.
Cell Proliferation: Changes in membrane potential (Vmem) regulate cell division, influencing tissue growth and repair.
Cell Differentiation: Bioelectric signals modulate stem cell differentiation into specific cell types, such as neurons or cardiomyocytes.
Cell Migration: Transepithelial electric fields direct cell movement, critical for wound healing and embryonic patterning.
Cancer Suppression: Bioelectricity influences cancer cell behavior, with abnormal signatures revealing tumour sites and the signal of the healthy cells turn tumour cells back to normal behaviour! (Michael Levin)
Pattern Memory: Bioelectric networks store anatomical “memories,” guiding cells to rebuild specific structures, as seen in two-headed planaria.
Collective Intelligence: Bioelectricity enables cells to form networks that process information, coordinating multicellular decision-making.
Left-Right Asymmetry: Bioelectric signals establish body asymmetry in early embryos, determining organ placement.
Neural-Like Cognition: Bioelectric networks in non-neural cells exhibit proto-cognitive functions, like memory and decision-making, akin to neural processes.
There are most certainly billions of #NANOROBOTS involved in the assembly of nanotechnology.
Again I find Myself rather overwhelmed and keep wondering, so what do We do about it?
Any suggestions?