Mystery Solved! The Bill Gates "Trade-Secret" Qdot (LNP) Patent shows Charge Fluorescence & ECL for "Genetic" Sequencing: They are mapping, reading and writing Voltage Language, not Genetic Code! (V)
LNP = Qdots = Voltage to Light and Light to Voltage /// Decyphering Reality /// For what its worth /// The future is offline
Good Morrow! Let’s get straight to it: Qdots (nanocrystal semiconductors) were meant for “genetic” sequencing (besides their presence in medications, as adjuvants, as LNP in the shots, in “antiviral” aerosol injections etc., as labels and voltage fluorescent agents). Qdots are the “mRNA” messenger “molecules”1, that transcribe voltage to light: They are voltage sensitive and turn that into light (through fluorescence)- which can be transduced to EM signals (mesogen fibers). The patent explicitly states their presence in mixtures of oligonucleotides (or primers) for PCR(this is why Bill Gates considered it a tradesecret and removed it from the thermofisher website). Read the whole patent (I luckily had a copy before it went offline from Thermofisher for some considerably obscure reason… it is now back in the patent archive). Rosalind Franklin discovered Graphene particles with a 10-100 nm size in 1951!
Qdots are taken up by our cells- through endocytosis, just like imaginary “viruses”…
Cyphers!(This document is evidencing the plausability for a cypher from Voltage Gradient information of biological materials- to DNA Code. This is the magic trick of the masonic PCR fraud.
The imaging devices (qdots) were called “Lipid Nanoparticles” and the cytotoxic protein coronas with nanoparticles (the viruses) around all forms of graphene dot assemblies, were the “spike proteins”, because of the natural protein corona they form.
The elemental compositions of the mythical “SARS-CoV-2 spike protein” and a 5 nm graphene quantum dot (GQD) with a natural blood plasma protein corona are strikingly similar, driven by the dominance of proteins in both systems. The alleged “spike protein” contains ~31.4% carbon, ~49.0% hydrogen, ~8.1% nitrogen, ~11.4% oxygen, and ~0.12% sulfur, while the GQD with corona has ~31.8% carbon, ~48.7% hydrogen, ~8.2% nitrogen, ~11.0% oxygen, and ~0.41% sulfur.
Fluorescence / Luciferase & Qdot LNPs ::: The Imaging of the Language of our Cells
Since the CockVide days, it was all about Fluorescence. 60% of what we are physically, is this charged emergence of intelligent and sentient cell electromes, communicating through ions and biophotons (which can be sensed and manipulated). The miracle of the witness though, is the ether bound element that cannot be reduced to photons or ions. Remember who you are manchild!
“At times, the entire scalp is illuminated“ (Qdots are highly UV reflective)
Dr. Ana Mihalcea demonstrating the fluorescence of “vaccinated” people, but also receivers of PCR and antigen “tests” - more code language for the distribution of fluorescent nanoparticles called Qdots, the LNP of the CockVide era.- sustained to this day & Mesogens are involved too.
It is all about voltage and fluorescence, as it is the case with the Qdot patent (trade-secret) and the dye used in PCR sequencing (or it is in the mixture for oligonucleotides, as described in the patent). Here is an example of a recent study about bioelectricity:
Abstract: "Translating the bioelectric code remains one of the core challenges to widespread biomedical translation of bioelectric interventions, as well as a better evolutionary understanding of how developmental ionic signaling became the basis of neural intelligence. Thus, it is essential to develop model systems and protocols in which diverse bioelectrical parameters can be quantitatively studied together, in the living state, and connected to cell- and tissue-level outcomes. Here, we apply state-of-the-art quantitative Fluorescent Lifetime Imaging (FLIM) optical estimation of membrane potential (Vmem) to map the bioelectric dynamics of spreading Xenopus laevis neural crest cells over roughly 18-hour time periods. We identify a slow “analog” bioelectric component that functions on the scale of hours, and a faster “digital” component that acts on the scale of seconds. We then use information theory to show that digital NCC Vmem dynamics are largely distinct from calcium dynamics. Finally, we provide a survey of diverse bioelectric events revealing a deep complexity in collective bioelectric dynamics, likely involving tunneling nanotubes in their transmission, which suggests numerous avenues for further investigation." (Source post by Michael Levin)
This language… In order to CONTROL the bioelectric CODE - we must be able to read it. And you Transhumanists found a way to deceive us all, bravo (not related to the study- the applied experimentation around this is an archontic tightrope walk, it is virtually dissection and frankensteinization of animal souls- but the results are truly mind boggling/ life changing! ...Excerpt about Bioelectricity from the study mentioned above
Mystery solved: Voltage Sensitive, Fluorescent Qdots (the LNPs in the CVD shots) are specific ingredients for the “GeNeTic” Sequencing Process!
Release the voltage gradients and be there light (Qdot Fluorescence)!
They are using qdots for the oligonucleotide mixtures used in genetic sequencing. Now we know where the data is coming from, cyphered into genetic information. What’s more, they describe the ion channel pump system in great detail and its signal transduction through qdots…there we go!
So the qdots are both voltage sensitive and sensitive to light frequencies in a broad spectrum. Therefore, the smartphone or any one of those smart LEDs can be used to excite them. They are sensitive to all of our important bioelectricity. Nobody asked for this atrocity. Surprise, light information signaling is able to perfectly tune Qdots:
"We can control the bandgap by controlling the amount of energy we introduce into the sample, and we control the amount of energy by controlling the light," Abolhasani says. "This allows us to tune the bandgap very precisely.”
This is Bill Gates beloved trade-secret (the patent is in the archive now). It shows that Qdots could be the secret ingredient of the dyes or concoctions of oligonucleotides for “sequencing”. …just like they do it with medication, they sneak in the qdots that aid the registering of information about the electrical properties of the material, or inside living cells, the ionic charge (potentials)!
Marsh and Beams discovered the electrical properties of chromosomes (1946) … “The electric field caused the mitotic spindle to align parallel to the field lines, altering the plane of chromosome segregation. This suggested that the spindle’s microtubules, being polar, respond to electric fields via electrophoretic forces or dielectric properties”.
So maybe it is all about the electrical properties of the chromosomes … the antenna unit of our bodies so to say ? Do they maybe want to extract all possible information about these? The length, thickness and composition of the chromosomes varies wildly across species and plants have extra variability… maybe they wanted to study them for their electrical interfacing without telling us what they are capable of as antennas for our biological functioning. New sequencing methods are already openly admitting to read voltage with a semiconductor chip - with a fairy tale cover up about the mythical genome…
This is how it could work, through the Electrochemiluminescence of Qdots with buffer chemicals :
Extract showing the bioelectric life of explanted frog cells:
The visualisation of the bioelectric, voltage based communication of cells (through staining and imaging techniques…) - by Michael Levin:
Controlling Bioelectricity over the potentials of our cells membranes means controlling the action potentials of our neurons. Patterns of thought, feelings- any state can be recorded and radiated back in voltage gradient language (so the frequency is merely the rhythm / intensity of the signal (secondary), the voltage gradient and how it distributes over cells is the primary message), which is basically the “prompt” for our biological intelligence, the electromes that govern our body, connecting through the Aether, with a touch of irreducible magic, the witness and subjective experience of natures splendour, all these familiar forms governed by kindred Electromes!
They react to touch and sometimes they move without being stimulated by touch - they have agency and sense their environment. They can latch on to the finger like an octopus- once attached, it is difficult to get them off. (at 28:00 mark)
Interesting: Justin Coy mentioned that the mesogen fibers are attracted by polymer clothing!
Pfizers fluorescent dye called “cellTrace” Calcein Red-Orange- promising GREAT “biocompatibility” and membrane voltage signal transduction into light signals that can be relayed and red by our smart devices, processed by A.I. (and back)
They speak about “vaccination record tattoos” and the microscopy resembles the glowing of the heads of people and that Pfizer spoke about screening the vaccination integration through the injection of luciferase. Now, Coy misinterprets the “genetic” step of how Luciferase makes “the Genome” fluorescent, because this is the cypher for its voltage sensitivity(the trade secret again) :
It is clear, that voltage sensitive elements are on all the new sequencers, using semiconductor chips and there is a narrative to distract with PH / acidity as the aspect of interest, when it the charge that is measured.
Charge information about the biological material (Chromosomes etc…), cyphered into the “Genetic Code”
Mapping the electrical properties of the chromosomes in the world!
“In summary, Qdots provide a powerful tool to study biological materials by offering information on their size, conjugation efficiency, stability, charge, and specific interactions with the biological material, all while enabling sensitive and multiplexed detection (different sizes for different wavelength and the signal fuses and can still be reconstructed).”
A thought Experiment
A standard gene sequencing setup (thermocycler, laser, PMT/CCD) can be repurposed to study temperature-dependent reactions of QD-labeled chromosomes (differently tuned graphene qdots with specific coating that aids readings) , providing electric information. (Resistance, Conductivity, Information about the Material and how it reacts…which can identify it with all the primers and inputs)
Setup:
Use a thermocycler to cycle temperatures (25°C, 37°C, 60°C, 80°C) on QD-labeled chromosomes/fragments in PCR tubes or capillaries.
Excite QDs with a 405 nm laser (standard in sequencing) and detect emissions with a PMT/CCD, converting light to voltage (0–5 V).
Image in-tube (real-time PCR-like) or post-cycling in a capillary (Sanger-like).
Temperature Reactions:
Protein Conformation: Voltage drops at 60°C indicate unfolding (e.g., 2 V at 37°C to 1 V at 60°C).
Chromatin Condensation: Voltage peaks shift, reflecting density changes.
Charge: Voltage intensity changes suggest charge alterations.
Graph:
Voltage vs. temperature: Shows intensity changes with temperature.
Voltage vs. time: Tracks dynamic responses during cycling.
Voltage vs. position: Maps fragment or structural changes in capillaries.
Electric Information:
Structural (protein distribution, condensation), charge, or organizational data, akin to pre-1952 cytogenetics, quantified electrically.
Standard Setup:
Feasible with standard thermocyclers and sequencing laser/detector systems. Minor adjustments (e.g., filters, sample format) stay within standard equipment.
This approach repurposes the sequencing setup’s thermal cycling and fluorescence detection to probe chromosome physical properties, meeting your goal of a different purpose. If you want to focus on a specific aspect (e.g., in-tube vs. capillary, QD type, or chromosome feature), or if the Substack article provides critical QD properties, please clarify, and I can refine the answer further!
A Laser excites the Qdots and gives information about the surrounding material (Chromosomes). A buffer can aid electrochemical excitation of the qdots (one special property) in relation to that material. Maybe it is about the Resistance, Conductivity, Reactions, when excited by IR light / voltage etc…
Detection by Camera and Voltage Conversion
Optical Detection:
The qPCR camera (CCD, 500-650 nm sensitivity) detects QD fluorescence (600 nm) and potential ECL from QD-TPA interactions during annealing (60°C, 20 s).
Electrochemiluminescence (ECL) adds data on charge dynamics, local electric fields, protein-charge interactions, and conductivity, enhancing electrical reaction insights compared to photoluminescence.
Fluorescence intensity scales with QD excitation; ECL is weaker but detectable with high-sensitivity settings.
Reading fluorescence from QD-labeled, genome-less chromosomes in a microfluidic gel electrophoresis setup is highly feasible, providing detailed optical data on chromosome structure and quantity, far surpassing pre-1952 staining or microscopy. Deducing bioelectric properties (voltage, conductivity, resistance) from fluorescence is theoretically possible by correlating intensity or spectral changes with electrical phenomena, but it requires calibration, modeling, and high-resolution detection. A realistic scenario involves a microfluidic chip with fluorescence imaging and computational analysis to estimate bioelectric properties, offering a novel but experimental approach. This is a modern innovation, not comparable to pre-1952 capabilities, and while promising, it needs further research to achieve precision.
Document showing how Bioelectricity is red by this new voltage sensitive semiconductor, then how they use cyphered language to explain it in the "genetic" paradigm to hide the simplicity of bioelectricity and the power of prompting our biology with it, basically !
The“CYCLING“ enhances the signal-to-noise ratio, protocols behaviour under certain temperature strains - all the information about the chromosomes of all life forms, because the functioning of our cells depend partly on their physiology, as antennas perhaps!
The new Ion series from Thermofisher have replaced the laser with a semiconductor chip that is reading “hydrogen” Ions !
… let me remind you that before, it was all about the alleged fluorescence of oligonucleotides, when, in fact, the fluorescent source were the qdots that are transmitting very detailed information about the surrounding materials that can be translated into conductivity, resistance and other measures. This information is cyphered into the “geNeTiC coDe” and the cycles are the temporal dimension of such bioelectricity readings camouflaged as “DNA code”.
They are stretching this monumental lie to a degree of twisting that hurts my brain: “The “PHs voltage” is now red and allegedly tells them the order of oligonucleotides for the genetic code… This is hilarious, they call this the ION series!
Michael Levin can grow functional eyes on a frogs butt with the right prompt, we are watching him read the secrets of biology through the Electrome… It is all about bioelectricity, voltage, signals, morphic fields!
How “Chromosome Sequencing” can be done with Qdots (4 different waveforms can be seen in the software… stored separately from the “DNA Code” in a file) excited by the Laser:
A standard gene sequencing setup (thermocycler, laser, PMT/CCD) can be repurposed to study temperature-dependent reactions of QD-labeled chromosomes, providing “electric information” in a pre-1952 context:
Setup:
Use a thermocycler to cycle temperatures (25°C, 37°C, 60°C, 80°C) on QD-labeled chromosomes/fragments in PCR tubes or capillaries.
Excite QDs with a 405 nm laser (standard in sequencing) and detect emissions with a PMT/CCD, converting light to voltage (0–5 V).
Image in-tube (real-time PCR-like) or post-cycling in a capillary (Sanger-like).
Temperature Reactions:
Protein Conformation: Voltage drops at 60°C indicate unfolding (e.g., 2 V at 37°C to 1 V at 60°C).
Chromatin Condensation: Voltage peaks shift, reflecting density changes.
Charge: Voltage intensity changes suggest charge alterations.
Graph:
Voltage vs. temperature: Shows intensity changes with temperature.
Voltage vs. time: Tracks dynamic responses during cycling.
Voltage vs. position: Maps fragment or structural changes in capillaries.
Electric Information:
Structural (protein distribution, condensation), charge, or organizational data, akin to pre-1952 cytogenetics,quantified electrically.
Standard Setup:
Feasible with standard thermocyclers and sequencing laser/detector systems.
This approach repurposes the sequencing setup’s thermal cycling and fluorescence detection to probe chromosome physical properties. (A very real possibility!)
They are describing Qdots, nucleating to the cells membrane or entering the nucleus (seen in Karl C. Microscopy)
This is the greatest cover up in the world so far, these cationic nanoparticles with lipid around are Qdots, meant to bring voltage to light and back- with a lot of electrochemical sensitivity too! This is why they have mapped the chromosomes of the world!
We are the Chip!
Michael Levin: “When you have voltage sensitive Gap Junctions (an ION channel)- you have a transistor. When you have a couple of transistors, you have a boolean logic gate. When you have logic gates, you have truth tables and you can build- you know, whatever functions you want. Do you need to evolve the elements of that truth table? No you get it for free.” This is how they are actually hacking us. It is not the graphene itself, that is using BOOLEAN logic- it is very likely the hijacking of our cells relayed through the graphene that can manage that. Our cells are computing under their control, not entirely- but through the voltage sensitive fluorescence of qdots it is possible)! The studies are cyphered- just like they lie to us, by giving us wrong concepts about everything.
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Mystery Solved! The Bill Gates Trade Secret Qdot (lnp) Patent Shows Charge Fluorescence For Genetic Sequencing They Are Mapping, Reading And Writing Our Voltage Language, Not Genetic Code! (v)
Recap: So they are transducing our biofields voltage gradient language into light (and back), while interfacing it with our ubiquitous smart tech dynamically. Our biofield with consciousness is the Electrome2. This is therefore a type of “soul hacking”— that needs to be discussed. The capabilities of our devices are far greater than we have assumed, in the juxtaposition dissonance between genetics and “epiphenomenon”, where the right voltage gradient impulse can instruct the growth of a functional eye on a frogs belly. This discussion has been heavily suppressed, through general bamboozlement and disinformation stories. No one has clearly explained how it works and the genetic explanations are irrational dead ends.
Graphene & other self assembling materials (plasmonic nanorectennas for example) help against attenuation problems(the loss of signal strength in the visible light spectrum due to the tissues properties in our body fluids). These metamaterials help to transduce the signal to an electromagnetic one. There are electrogravitic effects playing into this, charging effects from the ether, much of which have never been discussed outside of black projects. We have been kept dazed and confused, with false concepts about virtually everything under the sun! And they are constantly showering us with these particles, allegedly to stop “mAnMaDe” “climate change”.
Decyphering Reality- For what its Worth
It is high time that all of us who feel this deep urge to contribute and brighten this orchestrated demise of a reality with a more worthwhile vision, collaborate and bring it forth! A vision that aligns with the principles of dignity and beauty beyond the constant rape through indifferent A.I. floods of irrelevancies, fake content and sensationalism, flickering in neon lights from every corner of our sold out home planet paradise.
I conjure those who feel, in their bones, that something profoundly important for our souls (Electromes) to breathe has been subdued far too long and it is high time that we become that and sustain it, add our lifeblood to a dream that can rescue this sinking ship of sanity. Graphenized but resilient, cracking the crusts on our eyes, to feel in the right way again. Anger for the perpetrators and compassion for people suffering under this enormous pressure of philanthropathic psychopathy!
If you are reading this, you are very likely also seeking for a way to undo the deceit and simply reveal the crime, let the criminals pay for this sick psychopathic game of inversions, the systematic destruction of our connection to our roots, while constantly blaming us for our situation that has been caused by this brutally inhumane monopoly end-phase situation we are stuck in.
So since we have all of this control technology going already, why don’t we also use it on them- for full transparency, resolve the rip off. No more forced Transhumanism, control the nanospace and EMF signaling mayhem- simple as that.
Let nature return and create as many commons as possible - respected areas and reduce all the signals overkill, beholding the damage done. Let the machines do the dirty work no one wants to do and we focus on bringing back humane relations with each other, nature and the world at large.
The travesty of inverting the guilt for the decades long blanketing of our skies with poisonous nanoparticles as climate change, while young folks are fed this demented narrative to glue themselves hysterically onto highways … The inflammation is then blamed on invented viruses and those toxic streaks in the sky are surely blocking the sun to reduce co2. Another demented lie- right into the core of our being, our lives, burnt into our minds for so many years - while claiming to fight disinformation. A world of inversions indeed !
It is quite a smart move, to let people scream viruses do not exist, when in fact- all the published science is actually measuring every single aspect of nanoparticle toxicity, effects on our cells, brain and more. So they are not depicting something that is made up- while the perpetrators of such deceptions threaten us with fines for disinformation, for literally revealing the truth about a horrific deception that links our cellular voltage gradient language to the cloud, over magnetic and conductive materials in our blood (like graphene and qdots), which cause a certain fluorescence that can be transmitted by all the uninvited new self assembling sensations in our bloodstream. These particles form protein coronas that are cytotoxic and sterilising in our blood and they do resemble viruses 1:1 visually and by science.
As a reminder: When people start screaming “DNA does not exist”, it is an intelligently placed misnomer- because meant is the genomic story, Deoxyribonucleic Acid exists. Chromosomes are real too, they just separate though, for cell division- and no one is copying any genomes, except for the cryptographers from the CRISPR CAS9 crypto-science fiction novel of molecular fabulation.
The PCR is measuring voltage gradients over fluorescence of qdots in the mixes for oligonucleotides, for example. It is cyphered from voltage information through ion charges into the genetic code, so we are confused while they can read it all. So it is not fraud per se- it does measure bioelectricity and the results have patterns that match bioelectricity readings (utilising the same machinery).
Bill Gates is into computation, bioelectricity is basically that - hacking our biology directly and they use cyphered language for it, like “mRNA” (when Musk talks about all the possibilities of voltage gradient manipulation, without even mentioning it at all. He is a trickster). Meanwhile, Dr. Paul LaViolette shows us his collaborations for the B2 bomber and the UFOs with over unity energy through changes in electrogravitics, while the Archontic Clown Mr.Musk dumbs down the masses with his comical stone age propulsion driven rocket shows.
They have lured in most truth seekers with their cointel talking heads, driving them into space denial and flat earth theory, since the breadcrumbs of truth, from the (co)intel of our secret services- was enough to make the masses gullible enough, to swallow the flat earth card into absurdity. This has been done, mainly, to discredit the dissent entirely. But before we drive ourselves into unhealthy arrogance, I want to remind you that all of us fell for the genetic scam collectively, which should be a pretty humbling realisation at this point. The CRISPR cas9 stories are hilarious, how did we ever fall for this crap? But it also brings forth a momentum of liberation, to break the curse of deceptions and terminate the enemies of life!
The “Illuminati”/ Masons are illuminating our bodies - with voltage to light radiation (… and against our will)!
So this is how they truly “hacked” us! Quite a peculiar kind of enlightenment, not quite the 5D immersion as expected- our “Q”intel movements promised ascension- call the manager!
(They are having fun with us, in a philanthropathic way of course- the name lucifer comes from Latin, meaning "light-bearer" or "bringer of light" (from lux meaning "light" and ferre meaning "to bear").
They are illuminating our body, these illuminati - for them to interface us uninvited, while we suffer fast growth cancers and heart attacks. These philanthropaths do not deserve the air they are breathing!
Until next time! Your Bufus Alvarius
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It is time to tame the unhinged architects of a visionless but intelligent smart city dementia agenda- and have an open global dialogue about our most crucial technologies (which are violating the privacy of our soul), that rupture our minds and hearts through all the criminal narratives around them, that are inversely used to blame us into submission for the biggest scams in history (co2, viral disease, the genome, big data and wban data driven forensics, ancestry…”GMO” - they can basically do anything with plants and no one could notice if they make them look the same…), perpetrated to deceive and haunting our minds for millennia. Terrified vaccinated people were told that synthetic “unnatural” parts of “DNA” were integrated into their “holy genome”, effectively rendering them “marked by the beast” - which does not exist (the beast does exist, but it is just our maltreated planetary animal mother drowning in evil symbolism) …but that does not stop to terrify them horrifically. So let’s live up to the magnitude of this and draw breath to our own vision, breathing together (conspire - Middle English, from Anglo-French conspirer, from Latin conspirare: to be in harmony, conspire, from com- + spirare, to breathe), from alleged theorist to hands on practice ! The future is offline!
They nucleate to the liquid crystal cell membranes in our body and can even penetrate it- perfectly available hardware with natural transistor& memristor function and they grow liquid crystal spikes of graphene oxide that mingle with proteins in the blood…. the SPIKE PROTEINS!
The Electrome is an elegant concept introduced by Sally Adee, the publisher of the IEEE for 10 years, to unify the bioelectricity community and prevent misunderstandings, to deepen the intersubjective dialogue!
Hacking bioelectricity is described as “promting”- basically promting authentic intelligence!
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These Impulses can be pulsed from the opposite side of the body and it will be transmitted Michael Levin says!Different information patterns are trying to convince the other cells to join certain jobs, change team as well, according to the voltage gradient communication pathways through the Electrome.
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Michael Levin about nested agencies in life, consciousness everywhere! He actually mentions “meaning - around 47:00 in the interview, he says that the "platonic” space raises questions of meaning, rather than anything else.
Michael Levin talking about post-genetic realisations without going all the way:
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Everything that was attributed to the cyphered “DNA Code” was truly based on bioelectricity readings, through PCR, the new generation ION series from thermofisher, or by decoding the fluorescence readings through the qdots in sequencing, that take the voltage gradients from the organic material and turn them into light.
In our body, that can be relayed, transmitted to mesogens and red by bluetooth devices, radiated back from LED smart devices or your phones IR sensor. Welcome to transhumanism:
They are really trying hard to hide this (as I said, the patent got erased from the thermofisher website in 2022- there are all too specific explanations about the reading of ion channel systems):
When they program the A.I. to keep you in the dark but you won’t let it lie to you !
This new generation sequencer series with more temporal resolution through “cycling” is literally called ION “GENESTUDIO” - the cypher for voltage gradient readings, now with extremely high resolution… all of us have been fooled on a massive scale! This model is not using a laser anymore to register the “nucleotides” fluorescence, they are directly measuring the ions of “hydrogen” while distracting through “PH sensing” (or maybe they do that too) but it is all about the semiconductor chip with much better resolution of “nucleotide code readings” - when in fact, it is truly the bioelectricity, the voltage gradients over time that give all information.
They are now bending this monumental lie of gene sequencing, to drip feed us the bioelectric truth. “Converting pH changes into voltage signals” is the best joke in the document. It is the bioelectricity of the organic material that is measured. So they admit reading bioelectricity, but allegedly to measure nucleotides again ;) :
Document explaining how the new ION series works, basically how they hide their bioelectricity reading as gene sequencing and a thought experiment checking wether it could be used for bioelectricity mapping (which is what it's for)
There was an early revolutionary who saw the Electromes in everything, an animist / pantheist (who lived from 1548 - 1600) - he defended his views against all heresy acts threatening him and which eventually made him watch the daisies from below.
“Bruno's pantheism was not taken lightly by the church,[23] nor was his teaching of metempsychosis regarding the reincarnation of the soul. The Inquisition found him guilty, and he was burned at the stake in Rome's Campo de' Fiori in 1600. After his death, he gained considerable fame, being particularly celebrated by 19th- and early 20th-century commentators who regarded him as a martyr for science.”
We are all voltage fluorescent, free range live-“PCR” interfaced cellular computers / laboratory rats now!
🎯😉🙏 Are you able to share a link to that paper you sampled, I'd like to read the whole thing, to make sure I have the context right, and look at any supp. Info?
I'm very much liking your collective suggestion put forth in this stack, as I think your closer to the connecting missing piece than most out there. Ill be watching this space👍😉
🎯😉🙏 Are you able to share a link to that paper you sampled, I'd like to read the whole thing, to make sure I have the context right, and look at any supp. Info?
I'm very much liking your collective suggestion put forth in this stack, as I think your closer to the connecting missing piece than most out there. Ill be watching this space👍😉
Really great content. So good to see that someone is looking beyond the MAM ( mainstream alternative media) perspective. Excellent! Thank you!
Peace, love and freedom!