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DOES SCREEN TIME = SUICIDE RISK IN KIDS?

Discussion in 'Optimal Kids' started by Jack Kruse, Jan 30, 2019.

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  1. Jack Kruse

    Jack Kruse Administrator

    PARENTS screen time increases the likelihood your kid will commit suicide.

    A doctor friend of mine who recently killed himself in Jan 2019 never saw the AM sunrise either. How did I know this about him? .......because I asked him at an AMMG meeting in Orlando 6 years ago. He told me his testosterone protocol would remedy that problem.

    How did that work out for him?

    What didn't he know that I want you to know about your kids? Why wasn't Uncle Jack surprised?

    Screen time is linked to suicide via the butterfly effect of light on POMC and dopamine.

    He did not know what Jack teaches about depression/POMC/AM sunrise.

    More proof that getting AM sunlight to program your RBCs is the key to avoiding depression, mental illness, and suicide. Why do I say this? Because red blood cells (RBCs) modulate innate immune responses by scavenging chemokines from blue light and nnEMF damage. Keeping your RBCs in tip-top shape is one of the best antidepressants I know of. This helps explains why parabiosis studies show so many health benefits with blood that is younger from a circadian standpoint and has an ability to clear these molecules, so I have hypothesized that RBCs may attenuate CpG-induced inflammation in multiple organs through direct scavenging of CpG-containing DNA released from damaged cells.

    The innate immune system appears to use TLR9 on our blood cells for detecting unmethylated CpG dinucleotides which are liberated during the blue light hazard and nnEMF exposure associated with mental disease. The CpG Islands help tell the immune system how much damage has been done by pathogens. Why? CpG islands in pathogens vary compared to our own from our DNA/RNA and mtDNA. CpG islands are relatively common in bacterial and viral genomes but are highly methylated and uncommon in vertebrate genomes. THIS IS WHY AM SUNLIGHT IS IRREPLACEABLE WHEN YOU ARE DEPRESSED AND CONSIDERING SUICIDE, in my opinion. The sunrise is the surprising best drug designed by Nature to keep us from death = this is why POMC makes the chemicals it does in the eye and skin every AM you have your skin in the game.

    It has also been shown in the literature that RBCs homeostatically bind mtDNA, and RBC-mediated DNA scavenging is essential in mitigating tissue injury after CpG-DNA is liberated from heme-based proteins from destroyed cells. What kind of disease states should we expect to see cf-mtDNA elevated? Any disease where inflammation is induced by heme protein destruction = blue light hazard, depression, nnEMF, sepsis, trauma and most mitochondrial and RBC diseases tied to alterations in circadian biology. All neurodegenerative diseases fit this bill too.

    What protein controls circadian cycles in RBCs? Peroxiredoxins.

    They are also heme-based proteins in our RBCs. Peroxiredoxins affect the PER protein function by way of ferroptosis in the circadian clock gears of cells and this is where depression begins in humans. It begins even earlier in kids who are afflicted with the blue light hazard before their brain is myelinated. When will we wake up to the power of sunlight over man's drugs?

    Don't believe me? ------> https://www.sciencedaily.com/releases/2017/11/171130170212.htm

    Still don't? ----->https://www.abc.net.au/news/science...s-vulnerable-to-mental-health-issues/10751264
     
  2. Jack Kruse

    Jack Kruse Administrator

    Screen time increases the likelihood of Adrenal Fatigue.
    How?
    Screen time is linked to AF via the butterfly effect of light on heme-based chromophores/ferroptosis/POMC/dopamine.
    Most people have no idea it is a topologic defect caused by nnEMF in our environment that alter how the photoelectric can interact with our cells.
    More proof that getting AM sunlight to program your RBCs is the key to avoiding AF?
    This podcast gets into this photoelectric problem.
    https://drsherrillsellman.com/podcast/audio/wwmk/WWMK_012419.mp3

    ^^^^THIS PODCAST WAS DONE BEFORE Dr. C KILLED himself.


    When your eyes, skin, gut, or lung surface are afflicted by nnEMF trauma it induces cell damage in heme-based chromophore proteins that liberate something called CpG Islands from our nuclear DNA/RNA or our mtDNA from the cytochrome proteins like cytochrome c oxidase.
    It has also been shown in the literature that RBCs homeostatically bind mtDNA, and RBC-mediated DNA scavenging is essential in mitigating tissue injury after CpG-DNA is liberated from heme-based proteins from destroyed cells. What kind of disease states should we expect to see cf-mtDNA elevated? Any disease where inflammation is induced by heme protein destruction = blue light hazard, ADRENAL FATIGUE, depression, nnEMF, sepsis, trauma and most mitochondrial and RBC diseases tied to alterations in circadian biology. All neurodegenerative diseases fit this bill too.
    What protein controls circadian cycles in our surfaces I mentioned above? Sunlight induces changes in tissues below these surfaces. What gets programmed just below these surfaces? RBCs? What is in RBCs? Peroxiredoxins, cytochrome c oxidase, hemoglobin, catalase. All of them are heme-based proteins. Most of them are inducible proteins too. This means that the environmental EMF or oxygen levels induce their production. This is how biochemistry varies in tissues. Biochemical pathways are not foundational. The electromagnetic fields around us induce the biochemistry in our cells.
    What do heme-based proteins due to the circadian mechanism controlled by PER1 protein? Peroxiredoxins affect the PER protein function by way of ferroptosis in the circadian clock gears of cells and this is where ADRENAL FATIGUE begins in human PVN in the brainstem. If you do not do this, eventually your PVN will become hypermethylated and be recalcitrant to most therapies. Why does the PVN get hypermethylated?
    Tissue damage in the nervous system induce ferroptosis and this liberates Vitamin A in the retinal aldehyde form and this aldehyde destroys the heme-based proteins I mentioned above. What causes methylation problems in the brainstem? The liberation of CpG Islands from our mtDNA and DNA/RNA in damaged cells.
    Red blood cells (RBCs) below our 4 surfaces need to be programmed by sunlight and no other electromagnetic fields. In this way, RBCs are the key modulators of the innate immune responses by scavenging these chemokines from blue light and nnEMF fields and damage.
    Keeping your RBCs in tip-top shape is one of the best treatments for adrenal fatigue I know of. Seeing the AM sunrise, avoiding nnEMF day and night, and STRICT avoidance of ALAN post-sunset is MANDATORY to get better.
    This Black Swan perspective helps explains why parabiosis studies in the literature have shown why young blood shows so many health benefits in disease states. Blood that is younger from a circadian standpoint, has the ability to clear these fragmented heme-based molecules from damaged cells.
    I have hypothesized in my Patreon blog series that RBCs may attenuate CpG-induced inflammation in multiple organs through direct scavenging of CpG-containing DNA released from damaged cells.
    How does our blood plasma link to this perspective Uncle Jack?
    The innate immune system appears to use TLR9 on our blood cells for detecting unmethylated CpG dinucleotides which are liberated during the blue light hazard and nnEMF exposure associated with mental disease. The CpG Islands help tell the immune system how much damage has been done by pathogens and how to react. Why? CpG islands in pathogens vary compared to our own from our DNA/RNA and mtDNA. CpG islands are relatively common in bacterial and viral genomes but are highly methylated and uncommon in vertebrate genomes. People forget mitochondria have a bacterial lineage and this is why mitochondrial damage leads to a hypermethylated state in our CNS and PNS.
    It begins even earlier in kids who come from parents who have AF, because those kids who are afflicted with the blue light hazard in their parent's germline occurs before the kid's brain is myelinated. A lack of myelination makes the child's brain more sensitive to nnEMF. When will we wake up to the power of sunlight over man's drugs?
    The innate immune system in our blood plasma also has another backup system to help RBCs out clear the toxins. It appears to use TLR9 on our blood cells for detecting unmethylated CpG dinucleotides which are liberated during the blue light hazard and nnEMF exposure associated with Adrenal fatigue and the development of cognitive haze and eventual mental disease if the stimulus is chronically present in the environment.
    The CpG Islands help tell the immune system how much damage has been done by pathogens and how they should induce the heme-based proteins.
    THIS IS WHY AM SUNLIGHT IS IRREPLACEABLE WHEN YOU ARE AFFLICTED BY ADRENAL FATIGUE, in my opinion. The sunrise is the surprising best drug designed by Nature to keep us from AF. This is why AM sunlight creates dopamine, melatonin, and POMC make 6 other key brain chemicals it does in the eye and skin every AM you have your skin in the game = This leads to BDNF creation that REVERSES the hypermethylation in your brainstem.
    This is BLACK SWAN MITOCHONDRIAC WISDOM HERE.
    Don't believe me? ------> https://www.sciencedaily.com/releases/2017/11/171130170212.htm
    Ya' still don't? ----->https://www.abc.net.au/news/science...s-vulnerable-to-mental-health-issues/10751264
     
    Karen & Glen C. likes this.
  3. Jack Kruse

    Jack Kruse Administrator

    Jason the Black Swan says,

    Less outside time + more devices = a downstream impact that negatively affects nearly EVERY aspect of health.

    Developing brains don't have a fully-developed myelin sheath that can tolerate these devices.

    A psychiatrist quoted in the article claims "the science at this time doesn't have the evidence to make .. recommendations." #mitochondriacwisdom

    Really? I got a stack of papers for her to review.

    https://medicalxpress.com/news/2019-01-screen-damper-child.html
     
  4. Jack Kruse

    Jack Kruse Administrator

    Many people argue that blue light in the day is needed so why block blue light from your digital devices!?

    ☀️ The issue with blue light from your screens is it’s unbalanced against other colors and at a specific intensity throughout the day, it doesn’t change intensity like with the sun

    The study below now proves that artificial blue light from your digital devices in causing apoptosis (cell death) in the human eye and is a complete game changer

    The study used blue light at 449 nm, 458 nm, and 470 nm. The results showed the lower the number nm (more high energy) then blue light the more cell death occurred in the eye.

    This shows that wearing blue light reducing glasses during the day is essential for your health when using digital devices or under artificial light indoors.

    If this causes cell death in the eye I am sure we will see future studies address my thoughts that blue light also induces aging and cell death in the skin.
    https://academic.oup.com/ib/article/9/5/436/5115388
     
  5. Jack Kruse

    Jack Kruse Administrator

    Lindsay Alfieri and Nardia like this.
  6. Jack Kruse

    Jack Kruse Administrator

    In a new national study, suicidal thoughts and attempts were reported in children as young as 5. Something has radically changed on Earth to cause this massive quick turn in suicide. Anyone want to guess what can cause a brain to stop thinking well so that it contemplates taking its own life? Every Black Swan knows what the cause is..........why don't you? https://www.huffpost.com/entry/yout...in-the-last-decade_l_5cab7b5ee4b02e7a705bc175
     
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