Watch the video above and head to www.daylightcomputer.com and use password KRUSE2023 to see more on this great innovation from Anjan Katta of Daylight Computer, based for now in San Francisco. Below is my receipt as the first customer of this innovation.

BLUE LIGHT IS A STIMULANT THAT CREATES ROS/RNS NORMALLY
And stimulants are 👍 great. Most Americans drink a few cups of stimulants each morning ☕️ to get themselves up to face the daily grind.
But you know what's not great? Being stimulated 24 hours of every day by blue light. This ruins the dose-response curve of the ROS/RNS. That is precisely what is occurring to modern humans because they live indoors and use tech screens excessively. What else is different about this version of blue light? The blue light that wakes us up in the sun is NEVER present without 42% IR-A light, which is red light. AM sunlight has 42% red light in it and only 1600K of blue light. This small stimulus of blue light is about to improve the executive function of the prefrontal cortex. This blue light needs red light to control the oxidation ROS/RNS that blue light makes when it is present without red light in our light environment.

ALL CELLS contain ion channels in their outer (plasma) and inner (organelle) membranes. Like other proteins, Ion channels are targets of oxidative impact, which modulates ion fluxes across membranes. Subsequently, these ion currents affect electrical excitability, such as action potential discharge (in neurons, muscle, and receptor cells), alteration of the membrane resting potential, synaptic transmission, hormone secretion, muscle contraction, or coordination of the cell cycle.
An important class of ion channels is the family of potassium (K+) channels; they are not only in charge of the membrane resting potential or the repolarization of the action potentials but also control cell proliferation or transmitter/hormone release, to name a few. A subgroup of K+ channels are the so-called calcium (Ca2+) activated K+ channels, which need either an increase of Ca2+ at their intracellular face to open or a combination of Ca2+ and voltage to function correctly. Maxi Ca2+-activated K+ channels, also named BK channels, constitute a subgroup of Ca2+-activated K+ channels.
Do you know where these ion channels exist in humans? They are found on the inner mitochondrial membrane. EXCESSIVE BLUE LIGHT exposure destroys these potassium ion channels to ruin signaling of cells that control the circadian mechanism and are associated with leptin and melanopsin. LET THAT SINK IN.
Mitochondria are a significant source of ROS generation targeting BK channels. Blue light creates that stimulus when RED LIGHT IS ABSENT.
C TERMINAL CHANGES ARE A BLUE LIGHT STORY.
The inner membrane of mitochondria contains BK channels (mtBK), which appear essential in the production of ROS. mtBK channels appear to be inserted into the mitochondrial membrane with the toxin binding sites for charybdotoxin and iberiotoxin exposed to the mitochondrial intermembrane space. This can be accessed using outside-out patch configuration of the inner mitochondrial membrane. Consequently, the C-terminal tail domain, including the Ca2+ binding site, is localized to the mitochondrial matrix where the proton gradient exists.

RED LIGHT MOVES PROTONS BEST. Blue light creates the most ROS. Do you understand why subtracting red light and UV light from blue creates mitochondrial diseases now?
Your brain wakes up when you look at your computer or phone screen. It's alert. Because it hears, "It's daytime! Time to be focused and do human things!"
But guess when it's terrible to hear that signal?
The other 14 hours of the day, the Sun wouldn't usually send such a signal to the brain.
We need a break from the stimulus. Otherwise, we fry our circuits and get fatigued.
So take a break from the blue light our modern world worships. Stop the intravenous coffee to your SCN and allow yourself to relax.
WHY DO ALL HUMAN NEED THIS COMPUTER?
This computer builds your brain anabolically and does not destroy it catabolically as every other computer does.
WHY DOES ALAN (artificial light at night) or blue light cause melanoma?
Pyrimidine dimers are molecular lesions formed from thymine or cytosine bases in DNA via photochemical reactions. Ultraviolet light (UV) induces the formation of covalent linkages between consecutive bases along the nucleotide chain in the vicinity of their carbon–carbon double bonds. The dimerization reaction can also occur among pyrimidine bases in dsRNA (double-stranded RNA)—uracil or cytosine. Two everyday UV products are cyclobutane pyrimidine dimers (CPDs) and 6–4 photoproducts. Blue light causes these cyclobutane residues, which can lead to cancers like melanoma. Many people think UV light causes this, but blue light is way more potent in generating these melanoma-inducing chemicals, as shown below.
These pre-mutagenic lesions alter the structure and possibly the base-pairing in DNA. Up to 50–100 such reactions per second might occur in a skin cell during exposure to sunlight but are usually corrected within seconds by photolyase reactivation or nucleotide excision repair. Uncorrected lesions can inhibit polymerases, cause misreading during transcription or replication, or lead to arrest of replication.
You might not know pyrimidine dimers are humans' primary cause of melanomas. Your dermatologist certainly does not know this science. https://www.nature.com/articles/s41467-020-16283-9



THIS IS NOT A MOUSE STUDY
Artificial man-made Blue Light "Enhances" Melatonin Suppression….via melanopsin damage………Imagine that?
🐭😱
I'm sorry, but we are still relatively close to the starting line when it comes to the amount of research into blue light and circadian rhythm so we kind of have to read what we have access to and do our best to be DIRECTIONALLY accurate in what we take from them and how they apply to humans.
This paper, however, is one of the best you'll find anywhere.
They tested 24 humans. Some of whom, I'm told, actually look like mice.
They determined...
"Each fluence-response curve demonstrated that increasing corneal irradiances of light-evoked progressively increased nocturnal melatonin suppression. A comparison of these fluence-response curves supports the hypothesis that polychromatic fluorescent light is more potent for melatonin regulation when enriched in the short wavelength spectrum."
Download this 30-page PDF beauty as an early Christmas present here: https://jdc.jefferson.edu/cgi/viewcontent.cgi

WHY DO I WANT TO EXTINCT BLUE-BLOCKING GLASSES?
Is there visual acuity flux in the human eyes due to variable factors in our light environment? Yes, there is. Black Swan MDs would be wise to recommend routine sunning the eyes to release stress in eye ciliary muscles to improve vision accommodation via dopamine modulation of the skeletal muscle fiber types in these eye muscles. Just knowing this data is true, one can't help but wonder if prescription eyeglass wearers shouldn't be evaluated in an eye doctor's office over a series of days/times (diurnal exams) to account for these confounding lighting factors in determining overall average visual acuity. I’ve begun doing this for blue blockers. The results are quite interesting. It caused me to ask Anjan to build this computer. Blue locking glasses are not enough protection.

Based on my work with patients, a computer with zero blue light emission is the requirement. We will still need them for other things, but you won't need them with Anjan's computer.

There is a “revolution on the surface of the earth” called blue-lit technology, and it is causing a new evolution of free radical signals via nnEMF and magnetic fields from your environment, changing the internal terroir in your mitochondria, leading to diseases that appear to emerge from nowhere. Anjan's computer puts a dent in this game plan hatched by Silicon Valley. This is why they want him to fail. The healthcare reality you obtain manifests from these collisions and creations.
SUMMARY
This conversation happened recently based on my work around decentralized medicine and anabolic computing in El Salvador.
Follow me closely with this, because this might be the most important post you read on Patreon in your entire life:
"I have known for years now that melatonin is anti-cancer. But every study I’ve read basically pegged it as such because of its antioxidant activities. This is true to an extent.
However, last night, a pretty brilliant neurosurgeon that I’ve been following for about five years now turned the light on in my mind and made it crystal clear to me precisely what the mechanism is that makes melatonin so crucial for cancer prevention and healing from cancer.
He made two statements:
1) blue (artificial) light, especially at night, causes cancer.
2) nnEMF (non-native electromagnetic fields - think cell phones, x-box, tablets, Wi-Fi routers, cell towers, smart meters, smart homes, Apple watches, Fitbit, Bluetooth, or anything that operates on wireless technology) causes cancer.

But here is the connection that he helped me make last night:
What is the hallmark trait of cancer? - dysfunctional cells that are like STEM CELLS that are multiplying and growing out of control in the body.
Here’s the rub: we ALL have cancer cells growing in our bodies. All of us. What makes it that one person doesn’t develop deadly cancers while others do?
One word: apoptosis. This describes the body’s innate ability to recognize a cell as dysfunctional and potentially cancerous and “orders” the cell to shut down and die.
The amount of melatonin controls apoptosis a mitochondrion can make, and our mitochondria make the most melatonin in our body. That amount is quantized to the light we live under.
If apoptosis works correctly in you, you will not develop cancer because your body can recognize those dysfunctional cells and neutralize them immediately. Problem solved.
Here’s the thing: MELATONIN, the hormone made in every mitochondria and found in our pineal gland created in the absence of LIGHT, regulates apoptosis. Let me make this plain as day for you (even if it is a crude description of a very complex biological process):
No melatonin = no apoptosis.
No apoptosis = dysfunctional cells growing out of control = CANCER.
Artificial light at night and nnEMF BOTH individually signal to your colony of mitochondria that it is daytime. In response, your colony of mitochondria and your pineal gland will dramatically reduce melatonin synthesis and output.

The light bulb was invented in the last 100 years, and homes across America have permanently changed how they live. What do we do when the sun goes down? We flip on the light switch and turn the computer. We sit on our phones. On our TVs and tablets. We are using iPads as digital babysitters!
All of this lowers our melatonin and arrests the process of apoptosis.
We are literally handcuffing our body's natural and brilliant defense mechanism against cancer!
THINK ABOUT THIS FOR A MOMENT!
In our lifetimes, research shows that 1 in 2 of us will develop cancer. This is a VERY sharp rise from even 50 years ago.
We give money to cancer research charities, who then give that money to cash-rich pharma companies who don’t need our money so they can create drugs that don’t cure cancer and make us go broke using them. We run, walk, and bike for the cure.
What if the cure for cancer was right under our noses?
What if it’s as simple as shutting off the damn lights when the sun goes down? Use a computer that has zero blue light. We can all agree on using low amber lighting, wearing blue-blocking glasses, shutting off your Wi-Fi router, turning off your wireless devices, and instead of watching TV, hanging out and talking with your family and then going to bed early.
If it’s that simple to prevent cancer for you and your children, would you do it?
Below is a study that shows how melatonin regulates the apoptosis of cancer cells.
There are hundreds, if not thousands, of studies and research papers that show how artificial light at night suppresses melatonin and several studies that show how nnEMF does this as well."
"Jack and Anjan might have solved one of the biggest riddles in the world. "
CITES
1. https://pubmed.ncbi.nlm.nih.gov/24920214/
2. THE SIZE OF THIS MARKET IS HUGE https://bmcpsychology.biomedcentral.com/articles/10.1186/s40359-023-01166-7
3. https://www.socialworktoday.com/news/dn_121317.shtml
Steve Dorich
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