Knowledge, wisdom and insight all are valuable and all have a place in our lives. The difficulty lies in the fact that many of us are unclear as to their differences, often percieving the terms and their application to be interchangeable. Being clear and consciously aware of how our minds are engaged may be important to getting the most out of all three. While acquiring and applying information is valuable in and of itself, we also need to distill and judge that information, and ultimately find the deaper meaning and relevance to the whole of our lives. Perhaps the truest form of knowing is in acquiring all three, and understanding how they each enhance the quality and experience of life.
It has often been said that the greatest enemy of knowledge is not ignorance; it is the illusion of knowledge we have. Do you believe it? If not, why not?
How do you know you’re afflicted with this viral infection. Why does a Black Swan mentor tell his tribe constantly a half-truth always leads to a full lie?
Knowing a concept wrongly is more dangerous than skipping a concept when you are searching for wisdom. The illusion of knowledge is just like drinking too much wine with your beliefs. I’d suggest you never get drunk on your own dogma. This idea is simply stating that ignoring may not harm you as much as partial or incomplete knowledge may do. Today this idea is harming millions in the centralized world of healthcare and few realize it. They are inebriated with many false beliefs. Some people out there truly believe think they can help others with their incomplete knowledge but the reality is they are only creating deeper problems than a firm solution. This is the deep problem with the illusion of knowledge.
You better be careful out there in the world of online gurus. Who helps pack your parachute may not be the wise choice. My cognitive bias is 100% toward nature’s wisdom. She is the only lady I will dance with now. I believe most “parachute packers” cease to look for further information when they are arrogant enough to believe that have all they need already. My advice is simple.
At the end of every year, I write down and document my current beliefs. I started the process today. Then I try to toss out the things that are no longer solidly supported. I call this process, removing my “via negativa.” This is how I cut the superfluous from my life. When you develop a habit of updating your knowledge or facts openly, it becomes a vaccine against the “illusion f knowledge. This idea may help you at some point in your life. Rather than being completely ignorant, about the negative connotations of knowledge, if you ignore everything, then the world will ignore you. When you do this constantly rarely do you live with regret.
When younger, we make various choice’s without the future in mind. Sometimes those choices bite us in our mid-life. These are some of the things one might regret when they’re older.
1. Marrying the wrong person
When you’re young, check your motives for marrying. Don’t marry to copy your peers, or for social standing or out of pressure. Marry for love and companionship, marry the right person, marry your best friend. For if you marry the wrong person or for the wrong reasons, you will have to put up with that person the rest of your life. Things might get worse between you two; then depression, physical abuse, affairs, pain, shame, court cases, bitterness will define your mid-life years all because you chose the wrong one. Things will get worse when children are involved. Make the right choice of a spouse when you are young.
Time was passing like a hand waving from a train I wanted to be on.
I hope you never have to think about anything as much as I think about you.
2. The opportunities you did not seize
When you are younger many doors will open, you will get many chances. Many young people let these opportunities go because of fear, laziness, or pride; yet well younger and with more energy is the best time to start a venture and a name for yourself. Some think the opportunities are too big for them. Take advantage of them or one day when you’re older you will want to go back and grab those missed chances.
One of the greatest regrets in life is being what others would want you to be, rather than being who you were born to be. “Opportunities multiply as they are seized.”
“If a window of opportunity appears, don’t pull down the shade.”
Ideas that resonate.
3. The bridges you didn’t burn
Burning bridges in your past is understandable. It’s the bridges before us that we burn, not realizing we may need to cross, that brings regret.
When we are younger, we care little for relationships, what most think about is getting money and moving up the ladder of success at all cost. Many use and trample on people to progress, they take relationships for granted, messing up bonds, sleeping with people for personal gain. But these bad actions will catch up with you ahead. When you will realize how empty life is without love and friends. When you will have success but no one around you or no one to trust you.
I have learned that the stigma of “burning bridges” often holds people back from speaking out against tyranny and injustice. And if we want to build a better world, we need to encourage people to put aside their fears and speak up.
4. The child you aborted
You are a young lady, you get pregnant and you are scared. You take the aborting option quickly thinking of that moment then. But when you are much older, you will look back and wish you kept that baby. When you will be rich and successful you will wish that child you gave up on would be around to enjoy the fruits of your hard work. Being a single mother doesn’t mean you can’t make it in life or you can’t find a man in future.
As a man, a father, you stayed silent and let somebody choose for you. You forgot how deeply and unknowingly humans are connected. Life knows us all and plays with our interconnectedness. Were entangle to those who we did not speak up for or fight for.
In my opinion you’ll find in life, the most painful goodbyes are the ones that are left unsaid and never explained.
5. The child you rejected
Young man, you impregnated a woman, she told you she’s pregnant with your child. You rejected her and the baby and ran. But years later when you’re 50 something, you will wish you were responsible, you will wish you manned up and became a father to that child. You will see that child excel and become an adult but will have no claim to that grown child who you rejected from the beginning. You will regret being a Dead Beat Dad by choice.
The measure of a man’s success as a father is not just in the material things he provides, but in the love and guidance he offers his kids. Protect them by teaching them properly.
6. The marriage you destroyed
So you get married to your good fiance; the first months in marriage were good but shortly after, with your money and charm, you started having affairs. You became unfaithful. Your spouse begged you to stop, your children started hurting, your marriage was collapsing. One day when you are older, it will hit you how foolish you were to destroy the good marriage you had began to build for mere temporary thrills in affairs that did you no good. You will realize the damage you caused to your children and spouse.
7. The God you disowned
When you are much older you become wiser, God becomes more real as you see life in a more meaningful way. But don’t wait to get older to start enjoying a relationship with God. Know God when you are young, build your future with God. Don’t be a young rebel who runs back to God when age catches up and your time runs short.
The wound is the place where the Light enters you.
You are never alone. You are eternally connected to everything and everyone in Nature.
8. The body you messed up
You have only one body to live with all your life. The cigarettes, the alcohol you are abusing, the drugs you are taking, the unhealthy food you’re consuming; all that will destroy you slowly. When you are 50 and lifestyle diseases catch up with you, you will wish you took care of your body when younger, that you exercised more; but now the damage is done.
How we value and honor our own bodies impacts how we value and honor Nature.
There is a whisper we keep hearing; it is saying that we must build in us what we want to see built in the world. When we act from this truth on a global scale, using the lens of the body, we usher in the transformative opportunity of radical self-love, which is the opportunity for a more just, equitable, and compassionate world for us all.
9. The time you wasted
Time is our most valuable asset.
The time you are wasting when younger in worry, wrong relationships, laziness, being a couch potato, giving excuses and pursuing meaningless things; you will never get it back.
It is only when the clock stops does time reality come to your life.
Nicole Shanahan on time wasted: “Trump called RFK Jr. hours after he was almost assassinated, and the thing he wanted to talk about was childhood health” “If your head goes to ‘I wanna do the right thing with my remaining time on this Earth’ … that is a powerful thing. I think Trump was moved to a place of higher integrity. I’ve received hundreds of letters from people saying that we’ve been duped, but I’ve got to look at the sequence of events as critically and clearly as possible. Our goal is to use the leverage that we have to make sure that health is center stage. And I’ll tell you, nobody could have expected the kind of reception Trump gave Bobby this past Friday. No one. That was pretty special.”
10. The dreams and talents you shelved
Are you talented when young; are there things you love to do and you are good at them? Nurture those talents, exploit them, don’t give up even if you encounter set backs, don’t give up on your dreams. If you give up, when you’re older you will look at your peers who stuck to what they love and made it and think to yourself, “That could have been me”. Pursue a career, study a course you love. Don’t waste years of your life in a field that doesn’t fulfill you.
Most people’s dreams die a slow death. They’re conceived in a moment of passion, with the prospect of endless possibility, but often languish and are not pursued with the same heartfelt intensity as when first born. Slowly, subtly, a dream becomes elusive and ephemeral. People who’ve lost their own dreams become pessimists and cynics. They feel like the time and devotion spent on chasing their dreams were wasted. The emotional scars last forever.
Ideation without execution of the idea leads to its deletion. Dreaming is not enough. It requires doing to make it work.
11. The name you defamed
When you are older, a legacy is very important, the value of your name is crucial. You will ask yourself what is your reputation, what are you leaving behind? Your legacy is a sum total of your actions since youthful days. We write our biography by how we live life everyday. When you look back your path and you see the mud you threw at your own name, the shame you attracted and the little value you have added to the world; you will regret.
Everyone must leave something behind at death. What will you leave? My tongue is sharp because I am carving my legacy into beating hearts of the living. I’m not interested in carving cliches into tombstones. A legacy is etched into the minds of others and the stories they share about what you did in your life.
12. The wealth you threw away
Are you riding on good money during your productive years? Earning good money? Don’t throw away that money in clubs, reckless living and wasteful shopping. Invest with that money, widen your revenue stream, make that money work for you and keep it safe to take care of you in your older years. Leave an inheritance for your loved ones so that you will never say “I wish I knew better”
Time and money are almost always saved to be wasted. Realize it and learn this lesson. Buying something you do not need is a waste of money, even if it is a bargain.
What is the best way to help people? Make them keep the question and toss the thought.
13. The good love that got away
Is there that great person in your life loving you good? Don’t push that person away, or else that person will walk out your life and you will never ever find someone that incredible and who connects with you all your life. It will torment you to grow older with thoughts of “What if I was still with that person?”
When it’s gone, you’ll know what a gift love was.
When the sun has set, no candle can replace it.
14 The parents you despised
When younger, it is easy to show contempt to your parents; what do your parent’s know? They are old-fashioned, shady and small -minded. But your parents are still your parents whether you agree with them or not, whatever their style. Don’t let your parent die or age separated from you, reconcile and make up. When you get older, you will realize why your parents wanted to be close to you. The older you get, the more you see the value.
Don’t hold your parents up to contempt. After all, you are their offspring, and it is just possible that you may take after them.
Today is August 20th and we should have a full moon. This is a good day to improve your sex life. Why? Bright light and melanin is the answer.
It is estimated that up to one quarter of men have a low sex drive – defined as lack of interest in sex. Anxiety, stress, depression, and other psychological factors ARE correlated to low sexual desire in men, as well as a reduction in the male sex hormone testosterone. Anxiety, stress, and depression are all linked to lowered dopamine and melanoton levels. There is a deep reason lowered sexual function happens in simulataneously in humans.
Recent studies have found early morning exposure to bright light for just 14 days increased men’s testosterone levels, enhancing their sexual satisfaction.
The use of light therapy to improve sexuaL FUNCTION dates back to ancient civilizations, going as far back as the ancient Egyptians and Indians, who used sunlight (heliotherapy) for SEXUAL PERFORMANCE, healing and promoting health. The therapeutic use of light energy was more fully appreciated in the late 19th century when a Danish physician-scientist, Niels Ryberg Finsen, demonstrated the benefits of red and blue light in the treatment of lupus vulgaris and was recognized with the 1903 Nobel Prize in Medicine and Physiology. When these people were treated by Finsen he also reported these people also reported improvement in sexual function with increased desires for sex.
Seasonality has been shown to have a significant influence on sexual function by the increasing mitochondrial function in the central retinal pathways and in the pineal tracts. We know that the pineal gland in humans plays a key role in the neuroendocrine control of sexual activity. The retinohypothalamic tract carries information on the cycles light/dark to the suprachiasmatic nucleus of the hypothalamus that projects to the pineal gland and inhibits the production of melatonin. It also reduces the production of endogenosu melanin in these regions and this decreases the number of electrons liberated from water in CSF. When the number of electrons decreases, less light can be absorbed to be used in our semiconductive pathways in CNS in these regions. When these impulses stop (at night, when light no longer stimulates the hypothalamus), pineal inhibition ceases and melatonin is released normally.
UV light stimulates mitochondrial production of melatonin. Melatonin increases the secretion of prolactin, which contributes to sexual dysfunction in humans. AM sunlight inhibits the pineal gland tracts and this decreases blood plasma levels of melatonin. This activity shows us that the sun and light treatment favorably affect sexual function in humans by reducing plasma levels of melatonin.
The abscopal effects of light on the skin can also augment sexual function.
In 1960, the L.A.S.E.R. (Light Amplification by Stimulated Emission of Radiation) by Theodore Maiman was invented, based on theoretical work by Albert Einstein in 1917. This brought renewed attention to the therapeutic light energy field. The monochromatic, coherent, and collimated nature of lasers led to immediate interest in their biologic effects. In 1967, Endre Mester, a Hungarian physician-scientist, reported that low-dose laser treatments were capable of promoting wound healing and hair regrowth in mice. Both of these were related to melanin actions water to liberate electrons. Once the electrons are free the light can excite them and the body can use them to repair itself. He termed this phenomenon photostimulation and went on to demonstrate the efficacy of this treatment in human patients with skin ulcers. Many scientists, like Fritz Hollwich (book above) have noted that improvement in pituatary hormones with light therapy.
Men really respond to sunlight quickly. Many men are using drugs to improve sexual function and these drugs liberate nitric oxide in their sex organs as their main mechanism of action. You should be reminded that NO is stimulated by UV light exposure. This explains how UV light improves sexual function. The increased levels of testosterone explain the greater reported sexual satisfaction. In the Northern hemisphere, the body’s testosterone production naturally declines from November through April, and then rises steadily through the spring and summer with a peak in October. You see the effect of this in reproductive rates, with the month of June showing the highest rate of conception. The use of the artificial chronotherapy can really mimics what nature does.
THE MOON REFLECTS BRIGHT LIGHT AND THIS ALSO LINKS TO SEXUAL FUNCTION
Full moon happens on August 20th. Do you know what this means? In Latin, the word menstruation (or menses) and the word moon are linked. Perhaps it is an accident of nature or just pure coincidence that the moon takes almost 28 days to revolve around the earth, the same length of time most women have in their menstrual cycle. The study of anthropology has examined the tendency in traditional societies for women to ovulate when the moon is full and to have their period when the new moon has evolved. A lack of light source at night and reliance on the moon as a primary source of illumination is thought to be an important factor sexual desire and function. Bright light from the moon’s reflection stimulates LH surge which induces ovulation and sexual appetite. Women want sex when the moon is full due to the LH surge.
Melatonin peaks in women when they are having a period and is at its lowest point when they have ovulated. Melatonin also helps Luteinizing Hormone to be produced in the luteal phase and works with progesterone in raising a woman’s temperature. When you raise your temperature melanin acts to become a better electrical conductor. This would make sense in a pending pregnancy. It is also helpful in promoting the ovarian follicle to maturity and helps to do the same with sperm.
IT IS NOT JUST A MALE STORY: FEMALE SEXUAL DESIRE AND FUNCTION IMPROVE WITH SUNLIGHT TOO.
Heliotherapy helps treat women with low sexual desire and poor orgasm function because of the surge in LH. LH levels quickly rise just before ovulation. Men can smell women’s fertile phase when melanin is optimized in their olfatory tracts. This happens when their head and neck gets proper solar exposure. Normally, LH triggers ovulation in women. Lack of sun is behind many cases of modern female infertility cases.
A long-held centralized belief among anthropologists is that there’s no way to tell exactly when a human female is ovulating. Decentralized science now knows this is not true. Men were built to smell the LH surge of women because Mother Nature wants men who are seeking a mate to catch her in her fertile phase. Our olfactory cortex is paleocortex loaded with melanosomes so that massive amounts of electrons can be liberated in the olfactory nerve to improve the sense of smell. This cranial nerve only three layers and it’s physiologic ability is sensitized by the sun to make melanin. This charge separates water to make electrons, hydrogen and water. This would offer males the ability to know when the best time to reproduce. It turns out ovulation is a time that corresponds to when a woman enjoys sex the most as well.
In contrast to men whose every ejaculation during intercourse has the potential to result in pregnancy, conception for women is highly dependent on the ovulatory cycle because they are fertile only during the short period of time before and after ovulation. Ovulating women experience increased sexual desire, which manifests as physiological, cognitive, and behavioral responses (Gangestad et al., 2005). This phenomenon occurs because increased sexual behavior during the fertile window, which resembles the estrus of other female primates.
External signs in the skin predict sexual dysfunction. When skin cells responsible for pigmentation are exposed to estrogen or progesterone, the cells respond by adjusting their melanin production, resulting in either skin darkening or lightening. Although pregnant women often experience alterations in skin pigmentation, the reason for the changes has long puzzled physicians. Decentralized clinicians are no longer puzzled. Human females need a way to create more electrons when they are creating a child. This is why melanin & progesteron are upregulated. Progesterone increases water retention in women and melanin is used to split water into hydrogen and oxygen while liberatiing massive amounts of electrons for the developing embryo.
LH CAUSES A RISE IN ESTROGEN AND PROGESTERONE IN WOMEN
UV light in the sun stimulates the translation of alpha MSH in POMC. It turns out sunlight also stimulates LH to cause the upregulation of estrogen and progesterone. This the same signaling cascade stimulated by MSH via POMC. Human melanocytes express a separate, non-classical, estrogen receptor, called GPER, as well as a non-classical progesterone receptor, PAQR7. Neither receptor has been well studied in melanocytes. Soon you will see data that shows that sunlight can abolished the estrogen and progesterone effects by deleting these receptors. This will show that these relatively unknown sex steroid receptors are responsible for the skin pigment effects of melanin in pregnancy. HYPERLINK
The association between pregnancy and altered cutaneous pigmentation has been documented for over two millennia in humans. This has suggested that sex hormones play a role in regulating epidermal melanocyte homeostasis in fecundity. This makes sense when you understand that leptin controls fecundity, and leptin controls the circadian biology of estrogen, progesterone, and testosterone.
Human melanocytes that are exposed to higher estrogen levels after the LH pulse respond by increasing melanin production. Even the synthetic variant of estrogen called ethinyl estradiol, commonly used in birth control pills, has a similar effect on women.
Did you know that tamoxifen, used in breast cancer treatment, which blocks estrogen effects in cells, also darkens the skin. This is why it really helps in breast cancer cases. It is the melanin upregulation that increases its anticancer effect. You’ll never hear this from a centralized oncologist. After four days of tamoxifen treatment, the melanin content of the cells increased 200 to 300 percent. I learned about this side effect when my sister in law took the drug and I researced the effect it had on her skin and hair. Her grey hair vanished while she was on the drug and her skin darkened while she took the drug. This side effect of tamoxifen use represent a significant tanning response in the skin. Melanin’s light-absorbing properties allow it to absorb much of the UV radiation in sunlight and this increases electrons to heal the cancer and deuterim depleted hydrogen as an anti-tumor effect. There were other key effects I learned about tamoxifen as well. For example, tamoxifen induces the gene expression of catalase in melanocytes. This points decentralized clinicans towards the idea that the drug induces a promelanogenic effect mediated by ROS (hydrogen peroxide).
Catalase is a common heme based enzyme found in nearly all living organisms exposed to oxygen. All heme based chemicals are destroyed by blue light exposure. Catalse catalyzes the decomposition of hydrogen peroxide (H2O2) to water and oxygen. This makes sense because tamoxifen would simulataneously tan our skin and create more water to liberate more electrons to cure the cancerous state in the breast. It should be obvious to you why I made the slide below now.
In many tissues, when melanocytes were exposed to progesterone, melanin production decreased, causing skin to lighten. This points out why circadian mismatch of sex steroid hormones is often associated with cases of vitilgo. The use of progesterone by itself by many centralized antiaging doctors and probably is not a good idea when you realize it degrades melanin. It seems progesterone and melanin were designed to work in unison by Nature when women become pregnant. When they are light mismatched they work to harm women.
In women, pale skin, low NO levels, & low Vitamin D levels high correlate to poor sexual function, infertility and inadequate sexual satisfaction. Solar exposure increases LH production and melanin translation as a result of bright solar exposure. It is now well established that low LH is associated to low libido in women.
Solar light inhibits the pineal gland in the center of the brain and this allows for the production of more testosterone. There are many other positive hormonal effects associated with melanin production and solar exposure. We see this effect in triple negative breast cancers. This is one of the most deadly cancers women get in our modern world. Light therapy works awesome because it stimulates melanin production from POMC.
Our life becomes full when dawn comes to our shore. The secret to a good morning is to watch the sunrise with an open heart so it can energize and rejuvenate our mind and our sex lives.
The use of sunlight to improve sexual function can replaces the need for BigHarma medications. This lowers costs and comes with fewer side effects. These are massive goals in decentralized medicine in El Salvador. Just look at the effect UV light exposure has on breast cancer mortality. No one is telling women this but me.
Behavior precedes beneficial beliefs when it comes to solar therapy. Change requires a good beginning. that beginning must be sunrise. Beginnings are subject to implementation. Implementation precedes buy in and is hidden in passion of every renegade. When you make choices and you don’t implement them, your ideas may be the best ever, but they become the area most useless in your life. Ideation, without execution leads to deletion of all good ideas. So it is with SEX and the hormones associated with it.
CITES
1. Light therapy as a treatment for sexual dysfunction; focus on testosterone levels (Monday 19th Sept, 12.15-13.45)
D. Koukouna, L. Bossini, I. Casolaro, C. Caterini,A. Fagiolini.
University of Siena, Department of Molecular Medicine, Siena, Italy. University of Siena Medical Centre – Azienda Ospedaliera Universitaria Senese – Department of Mental Health
Our eutherian cousins that can still hibernate increase their brains’ ascorbic acid reserves before entering hibernation. This tells me they are increasing their ability to use magnetochemistry and the radical triad method in quantum mechanics I covered in the Decentralized medicine blogs. This helps water flow in aquaporins in the CNS and PNS using proton tunneling. Hibernation is linked to winter and a lack of environmental UV light, while cold temperatures affect changes in the leptin-melanocortin pathway. This increases endogenous UV light production from metabolism to increase ultraweak UV bio-photons. These actions increase blood glucose from POMC cleavage to act as antifreeze in the plasma. The light a semiconductor interacts with emits different light spectra, which can be used to complete different physiologic tasks in a cell.
Chronic cold exposure is the only thing that shuts down IGF-1 and mTOR simultaneously safely without affecting longevity or telomere biology. Why? Endogenous UV light controls mTOR biology and does not allow for changes in basal metabolic rate during starvation in hibernation. The endogenous UV light stimulates thyroid function, so BMR increases to help burn the animal’s fat stores during torpor. Moreover, the cold temperature causes insulin to become impotent and causes disease from insulin resistance because insulin loses its compelling power in cold below 62 F degrees. Insulin works biochemically differently in summer than in winter due to its temperature lability.
And here is the bigger shocker: Glucose is the only thing that can slow down timing the clock genes in front of every somatic mammalian gene. This allows it to control the ROS/RNS function to ensure timing is quantum precise. Getting the effect requires cold, so hibernation is linked to freezing temperatures when UV light is absent.
Contrary to popular belief, The Warburg effect, which uses glucose and glucogenic amino acids, has other roles for us because humans never face a proper winter. We lose the ability to see those effects, but they still operate in us when we get out of nature’s way.
Ketosis lacks environmental context, and not all versions of ketosis are equivalent. This is why a ketogenic diet is not always effective.
What is the proof of this: superoxide levels and ubiquitination rates…….and F:N ratios in mitochondria……..but no one is looking there; guys like Gary Taubes and Nick Norwitz and his food guru buddies need to back off the ketone measurements and focus on the real prize…….superoxide, ROS, RNS levels use for signaling in different tissues. Each tissue has a different threshold, and this is why ketosis is not a fixed problem for cancer. Food can never fix a quantum-based disease. Cancer is that type of disease.
It turns out that PD, AD, T1D, T2D, and AI all have super low superoxide pulses from their cytochromes because the blue light in those people’s environments is destroying circadian clock management in the leptin-melanocortin system. If you can’t make SO, you cannot enter autophagy to recycle redox-shifted mitochondria. And protons outflow from cytochromes is affected. The flow of electrons can reverse as well.
PHOTONIC OVER ELECTRONICS IS AN ANCIENT MEME THAT IS CODIFIED IN THE ART OF THE SPHINX
When this happens, you remain sick, have a lousy body composition, low T, low IGF 1, and become infertile regardless of how much fat you eat. To ……burn fat properly outside of torpor, mammals must see the AM sunrise. If they do not, this stimulates the torpor response. You never see the effect if you are not cold and ground as a mammal should be. And since evolution is about reproduction, if you’re infertile, it means you need to ask better questions to your food gurus. Not one of them will ever put this together for you.
Why don’t I see that from food gurus or biochemists? It is terrible for their business models.
Rest assured, there is a decentralized answer, and that answer is in SO and F:N ratios and the variation in voltages in cell membranes induced by light to alter your CO2 and BUN/creatine ratios. These exhaust fumes from metabolism link to the bio-photons spectrum you can create within your colony of mitochondria in a tissue.
You need to go back and really carefully read Warburg’s work. Few have. He found a prize about something other than glucose.
These altered distances and movements of mitochondria to the nucleus are critical in developing diseases like cancer. Why? The further the mitochondria move from the nucleus, the more pseudo-hypoxic the nucleus gets. The less O2 the nucleus receives, the less chance ROS and RNS are made. This tells us the Warburg metabolism is about trying to reset the lousy timing inside the cell from the effect of the light environment. The worse the circadian mismatch is, the more it favors a Warburg metabolism to limit ROS damage. Glucose allows for small amounts of ATP, and ATP is made more rapidly than it can be via the TCA cycle. The TCA cycle takes much longer at the quantum level to create ATP inside the cell. ATP allows the unfolding of proteins and provides water to engage the protons and electrons in those semiconductive proteins. In ubiquitination 5, we tackled this mechanism.
Now you can see why I do not believe the Warburg metabolism is terrible. The mammalian retina uses it to limit ROS/RNS because the retina is always photooxidized from light use during the day. Glucose is the emergency break for circadian clock genes that sit right before our somatic genes. nnEMF creates massive ROS/RNS while causing a decrease in CO2 and water production from a cell.
Today plants that evolved during the last CO2 famine will be the best plants to surround yourself with if you live in a nnEMF shithole. If you love the smell of gardenia, bourgonvilla, and magnolia, it tells me that your colony of mitochondria is not making enough CO2 or water.
Some will look at a plumeria flower (gardenia/magnolia) and try to tell us that its creation results from perfection in minimalism, but this only reveals what they do not know about thermodynamics. It is false. For me, it reflects the melanin sheets in their olfactory grove. People with lighter eyes and pale skin will be more drawn to these scents because of the lack of melanin in their three layer cortex in the olfactory nerve.
The Plumeria flower and the Trevi fountain represent opposite poles of the complexity argument I am explaining to you here. When life was simple, there was little oxygen, and we used glucose metabolism freely. A simple life requires simple biochemistry. Simple life always had a tightly coupled light and dark cycle because they had to exist by the dictates of their environments. Only eukaryotes can break this rule because they can change their environments. Humans are the most significant mismatch that Nature has built because of what their brains became capable of.
Did you know flowering plants like the plumeria species occur due to a lack of CO2 energy? So, their analogy is poor. They are minimalistic flowers/plants because of their low-energy environment. They are great examples of my point.
Plants also are made of DC electric semiconductors like we are. They reflect the light in their environment, structure, and phylogeny. Most plant groups were relatively unscathed by the Permo-Triassic extinction event, although the structures of communities changed. This may have set the scene for the appearance of the flowering plants in the Triassic (~200 million years ago), and their later diversification in the Cretaceous and Paleogene.
The latest major group of plants to evolve were the grasses, which became important in the mid-Paleogene from around 40 million years ago. The grasses, as well as many other groups, evolved new mechanisms of metabolism to survive the low CO2 environments linked to warm, dry conditions of the tropics over the last 10 million years. Beauty varies as environmental energies vary. Note the CO2 levels that PRIMATES EVOLVED. Note today, we are only at 420 parts per million. Modern humans forget that plants need CO2 to grow because of how photosynthesis works.
SUMMARY
Focusing on things out of your control, whether true or not, is a disempowering strategy. Focusing on methods and solutions to reverse a disease is better than treating it with a centralized Rx. This is what a decentrlaized leader advocates. The first responsibility of a decentrlaized healer is to define a reality that is a problem today and offer a durable solution. The last is to say thank you. In between, the leader becomes a servant to the public’s health. I plan to do this in El Salvador’s new healthcare system.
The take home: The periodicity of our clocks determines the shape of our lives. Time sculpts us. What happens in your colony of mitochondria every AM writes a story in the arteries of your flesh.
Question: My hubby tested very high and when I looked into it discovered it is an enzyme released by the white blood cells in response to inflammation and damage to the arteries. does anyone know how much research there is behind this marker and have any info I can take away?
ANSWER
Myeloperoxidase (MPO) is an enzyme stored in azurophilic granules of polymorphonuclear neutrophils and macrophages and released into extracellular fluid in the setting of inflammatory process and is associated with increased ROS/RNS creation due to altered mitochondrial metabolism and altered biophoton release. This is due to environmental changes that are not light/dark controlled.
The excess release of endogenous light is not creating enough UV light endogenously and this is not causing translation of POMC to create alpha beta or gamma MSH = less melanin inside and melanin inside deals with excess ROS/RNS production. As a result of this cascade, myeloperoxidase rises and it has been correlated with CVD disease because excess MPO has been linked as marker of plaque instability in PAD disease and coronary heart disease.
The cascade has many other parts associated with it discussed on the forum.
Without full spectrum sunlight, and total darkness at night PATIENTS should expect to have endothelial dysfunction and peripheral arterial damage should be EXPECTED by the decentralized clinician. It is not expected by each because neither are being taught properly about light. Light has no relative power without understanding darkness when it comes to ROS/RNS magnetochemistry. No one involved in any side of science in medical curriculums looks at the data in BigHarma literature to see this data much less understand the clinical significance.
A lack of NO production at our integument and eye surfaces ALWAYS link PAD by way of intimal thickening = directly to cardiovascular dysfunction. This is why MPO is an arterial disease marker. The local effect become generalized in the entire organ as the lack of NO production gets worse under ALAN or nnEMF influence. This is why PAD is always linked to cardiovascular disease. The link is the aberrant use of the electromagnetic spectrum to communicate to create NO. Modern light and RF and cell radiation impairs production of NO from arginine by eNOS. When melanin is missing in tissues arterial disease in that tissue is likely and MPO should be expected to rise.
This, in turn, induces high blood pressure by causing endothelial dysfunction. Mitochondria are intimately involved in importing nitrogen into tissues to create the substrates that eventually become NO when sunlight is present.
Nitrogen substrates are not created from the direct synthesis by eNOS. Nature provided the clue to me why humans got rid of Vitamin C for glutathione in this AMO physics dance. When Vitamin C is missing in subcutaneous tissues, glutathione become more reactive with locally produced NO. This mimics a radical pair or triad effect we see in avian compass navigation.
Here is more evidence of magnetochemistry in humans being used. When glutathione and nitric oxide are powered by terrestrial sunlight this allowed humans to produce S-nitrosoglutathione (GSNO). I think this is why human primates lost the majority of their integumentary hair and absorbed more melanin from the hair follicle to the interior.
SUMMARY
When we lost our dense mammal hair filled with melanin and it went to our interiors, this allowed the skin to become a better charge capacitor for the brain and heart by allowing the skin to become a photoelectric depot station to store massive amounts of nitric oxide. This is why human immune T cells are so common in the skin and why leptin was placed in subcutaneous fat.
Other primates do not have these phenotypes even thought their genomes are close to identical. This tells me magnetochemistry timing induced this evolutionary change. We never need genes to change this. We used timing to change the metabolic pathways in the skin using hair loss and removal of Vitamin C from the radical triad mechanism to do it. As a consequence of this dance using more light on the skin, keratinocytes were able to sense more visible light combinations with purple, blue, and green light to easily photocatalyze the release of NO from glutathione. The picture below explains why it happens. See how it affects eNOS production? Your centralized clinicians are abhorrently ignorant on how light and the non visual photoreceptor system operates.
Not only does NO liberation cause a relaxation of the blood vessels, but it also frees up glutathione to react with hydrogen sulfide gas to produce sulfate to make every other chemical in the skin water soluble to get access to body parts to have global effects in other tissues.
This is how light develops its abscopal effects. No one has figured out how this all works in humans but this is how I have seen it for 20 plus years.
To date no one has published a thing using my ideas. But I can explain why subtraction of Vitamin C in humans links to hair loss. Note below all the pathways that link POMC to Vitamin C, yet no one sees the connections. This also explains most of the integumentary and ocular diseases we see today because all have arterial disease as a preexisting condition.
This is why childhood obesity has changes in choroid always present if one looks for it. No pediatrician does. Most are not skilled enough to examine the retina directly in their offices
These change cascades due to light and dark alterations explains obesity, too. It explained to me why humans get aneurysms and AVMs in the brain as well. When you know better, you do better.
Fritz Popp earned a PhD in theoretical physics from the University of Mainz in 1969 and was awarded Professorship by the Senate of Marburg University. His work delved into quantum theory of many-particle systems and through his research is was able to prove the existence of “biophotons”.
WHY POPP NEVER COULD WRITE THIS BLOG SERIES EVEN THOUGH HE FOUND THE BIOPHOTONS STORY FIRST?
The reason is simple. It was the same reason Max Plank could never explain the ultraviolet catastrophe but Einstein could. Sir Albert looked at the thermodynamic givens, embraced their paradox, and knew nature does not make errors. His mind went deeper into the complexity of light. Planks gues right photons use quanta of light but he stopped there.
Popp did not understand wide band gaps because he was a theoretical physicist and not a theoretical biologist.
Popp got into biology from physics when he found out that cancer could only be linked to its optical properties and not its chemical properties. From 1970-2018 to his death he never explained the situation. I realized in 2005 I might have. Let me explain. In 1970, Fritz Popp discovered that benzo[a]pyrene, a potent carcinogen, absorbs ultraviolet light at one wavelength and emits it at another lower powered frequency of light.
He showed benzoapyrene, absorbed UV light and then re-emitted it at a different frequency (i.e. “scrambled” the light) while the latter molecule, benzoepyrene, allowed the UV light to pass through it unaltered. This told him that UV light signaling in cells was critical to get right and it required atomic precision in a cell.
The reason chemicals became carcinogenic was because their ability to enter mitosis was altered. Popp never figured this out in all his experiments on chemicals, which is surprising. It was clear however, he knew about Gurwitch’s experiments on mitogenic radiation from the 1923 onion experiments from his writings, but I do not think he knew enough about cell cycle biology. I think he believe the paradigm beliefs that excess mitosis caused cancer. The real answer was that mitosis is needed to avoid cancer.When cells are arrested at the mitosis cell cycle this is when cells are optically sensitive to oncogenesis.
UV light frequencies are clearly needed for cells to navigate all the steps in the mitosis phase of the cell cycle. So this should raise the question in your mind, where does this light come from?
WHAT DID POPP DO WITH THIS QUESTION?
This question led Dr. Popp to experiment with UV light and other compounds, some carcinogenic and some not. From his findings, Dr. Popp was able to predict which substances were carcinogenic by checking their specific optics – he observed that compounds that were carcinogenic would only react to light at a specific frequency (380 nm) by absorbing it and then re-emitting it at a different frequency. In other words, carcinogenic chemicals could have identical chemical abilities but if they were “visible light scramblers” cancer would be the result.
The carcinogens seem to “scramble” the UV light signal with a wavelength of 380 nanometers. 380 nm light corresponds to a band gap of 3.25eV. POMC responds ideally to the UV light 380 nm band gap. 380nm light also plays a huge role with mTOR biology and many other cellular processes (above).
This explained everything to me that Popp had found in his experiments. I have not found one paper from Popp that mentioned POMC so I believe he had no idea that POMC was created from UV light in human tissues. Without POMC there can be no melanin. Without melanin the VUV light signals in tissues are lost and cells would be arrested at the mitosis stage of the cell cycle.
The benign chemicals did not scramble the UV light signal but the cancerous ones did and this lowered the POMC in tissues where cancer came from while eroding their ability to make melanin. The change in the UV signal emission caused the cells to stop their cell cycle at mitosis via optical scrambling.
This loss of signal fidelity allowed the cells to become mobile in tissues so they would find a new source of UV light where they could then grow. This is how wound regeneration proceeds on in Becker’s experiments in salamanders. Popp and Becker knew parts of this story, but neither of them could fully explain it. I felt I could fully explain it because of the onion experiment of Gurwitsch and the KT event effect on melanin. There is one thing left to explain. Where do the biophotons come from?
BIOPHOTON TRANSFORMATION COMES FROM H+ LATTICE CHANGES IN THE MATRIX WITH 02 PRESENT
Time controls the flow of energy in matter.
Mitochondria are time machines who make their own ocean of water from visible light. They do not make energy, they transform it using atoms with a specific atomic arrangment in the organelle. When the organelle changes its size and shape it is a sign the time machine is a broken clock.
Energy transformation is not the sole function of mitochondria, since they have evolved as critical regulators of various cellular processes including metabolism, apoptosis, calcium buffering and cell division. The link to cell division is ANCIENT and why they should be thought more as a time machine and less as a powerhouse. Their reputation is misguided. Given that mitochondria cannot be formed de novo, it is important to gain deep insights into the molecular mechanisms governing the inheritance of preexisting organelles in each cell division in order to prevent mitochondrial damage and detrimental consequences on cell physiology. Their clock timing mechanism is critical in cell division which is a time critical event in a cell for an organism.
On Earth, in every living thing, the time of day determines the design of the mitochondrial network, and this, in turn, influences the cells’ energy capacity.”
Life uses the sun to tell cellular time. Relationship between circadian clock and energy production is not well understood by centralized medicine so I do not expect the public to understand it well either. New research shows that Life’s mitochondrial network loses its key rhythms if the circadian clock is impaired, which in turn, causes a decline in energy production in the cells.
The researchers showed that the circadian clock and mitochondria interact through a protein called the dynamin-related protein 1 (DRP1), a key mediator of mitochondrial fission. Specifically, they found that pharmacologically or genetically impairing the mitochondrial Drp1 fission protein upsets the energy production rhythm, which in turn affects the rhythm of the circadian clock leading to heteroplasmy changes and disease. This is how chronic diseases begin.
Mitochondrial fission and fusion cycles are integrated with cell cycle progression. A lack of ultraweak UV light is key in this process. Inhibiting Drp1 triggers DNA replication stress, which is mediated by a hyperfused mitochondrial structure and unscheduled expression of cyclin E in the G2 phase of the cell cycle. This persistent replication stress then induces an ATM-dependent activation of the G2 to M transition cell cycle checkpoint. Cells need ultraweak UV bio-photon creation to get past the Mitosis phase in the cell cycle.
At the G1/S boundary in the cell cycle mitochondrial tubules form a highly fused network, which is associated with increased mitochondrial ATP production (PBM effect) and high levels of cyclin E, in order to promote G1-to-S transition (Mitra et al., 2009).
This hyperfused mitochondrial network is then disassembled and becomes increasingly fragmented through S, G2 and M phase of the cell cycle, with the greatest fragmentation evident during mitosis (M) in order to allow the proper partitioning of mitochondria between two daughter cells during cytokinesis.
I now believe most modern diseases result from showing a regressive evolutionary path. This is called atavism. You heard that idea in this series already in QE #45. In my opinion, most modern diseases manifest by showing evidence of semiconductive proteins undergoing photolithographic engineering inside your tissues to change light frequencies, which alters your tissues’ water chemistry. This leads to new and alien bends, charges, and alteration of atoms in your tissues that change the morphology of your body and the physiology of your tissues. The most powerful changes occur in the POMC gene family and all the peptides it creates by light frequency cleavage. Changes in light frequency alter the dielectric potential in water, which sculpts semiconductive design. This is functionally how evolution occurs. It is not the path that Darwin put centralized science on.
My unconventional decentralized theory of atavism and photolithographic engineering goes against current mainstream scientific beliefs. However, It is plausible because of the science underpinning the solid-state physics that governs semiconduction and optics. While evolution plays a role in disease development, it is typically understood in centralized science via the lens of genetic mutations and natural selection = Darwinism The idea of light frequencies altering tissue chemistry and causing changes in the body is not well-supported by current centralized scientific evidence because no one in centralized science is allocating money to study it. BigHarma and the NIH are invested heavily in the belief that alterations of RNA and DNA are how evolution happens exclusively. They do not even allocate 1% of their funding to mtDNA studies. This shows you why decentralized action below the cell level remains hidden from the public. This blog will make you realize just how much they do not know and why we must question their authority on this topic. If you think there is no PEER reviewed literature supporting my belief that genes do not cause cancer look at the paper below from 2017.
MITOCHONDRIAL ELONGATION MIMICS GLOBE ELONGATION = DECREASED ENERGY
Thus, mitochondrial remodeling throughout the cell cycle is considered to meet the cellular energy demands during the progression of specific stages of the cell cycle, and to ensure faithful inheritance of mitochondria during cell division. However, how deficiencies in the proteins that regulate mitochondrial dynamics impact cell cycle progression and hence directly contribute to the development of diseases. Loss of Drp1 results in elongated mitochondria. Drp1 deficiency mimics what blue light does to the globe in myopia. It elongates the mitochondria. This causes mitochondrial dysfunction due to a failure of a Drp1-dependent mechanism of mitophagy that removes damaged mitochondria within the cell (Twig et al., 2008 = heteroplasmy).
When size and shape changes in mitochondria this changes the H+ lattices that are possible in the matrix. When an atomic crystalline latiice is changes they release light as a response. This idea is buried in the slide below.
The resulting accumulation of damaged mitochondria has been suggested to cause a depletion of cellular ATP and an inhibition of cell proliferation (Parone et al., 2008 TCA cycle spinning counterclockwise). Such an energy depletion-related cell proliferation defect may be caused by a metabolic checkpoint that triggers an AMPK- and p53-dependent G1/S cell cycle arrest (Jones et al., 2005; Owusu-Ansah et al., 2008). Persistent mitochondrial hyperfusion also induces centrosomal overamplification and chromosomal instability, which are causes of aneuploidy. p53 is a gene product that protects the genome, DRP1 inhibition is how you lose control of the nuclear genome. This is how DNA defects occur from mitochondrial peptide creation. = transgenerational epigenetics
KEY BLOG POINT: HOW BIOPHOTONS ARE MADE
Mitotic machinery transforms energy from matter (matrix H+ lattice changes from elongation) using oxygen and H+ to stimulate light release in the form of biophotons, which in turn, to regulate mitochondrial homeostasis.
Why is oxygen needed to make biophotons? You won’t find this answer in Roeland van Wijk’s book on this topic. You will find it here for 5 bucks. Oxygen is a powerful element for the human gut because of what it does to electrons. Oxygen use by life began the initial penetration of solving complexity in tissues and organizational structure. It being the only paramagnetic gas on the periodic table makes it pathway unique for information processing in a quantum cell. O2 has two unpaired electrons. Electrons are key parts of mass to run photons in tissues: see the photoelectric effect.
Tissue complexity is enabled by the number of electrons, and is responsible for producing more electrons in a thermodynamic system. This is why life exploded after the Cambrian event. There is no other reason. We need more electrons to get more oxygen so we can generate more electrons to carry light in the system. This is why humans lost their fur. Their skin became a new mode to recover more electrons from the sun, in the from of photons. Your skin is a solar panel for the complexity in your chest and brain.
Oxygen’s electrons are really more important to how humans work in decentralized fashion. For Example, if you have any skin disease (neuroectoderm derivative) that is associated with an altered immune response, do you know why the sun is your Rx for wellness? Did you know singlet oxygen is a potent trigger for the induction of human T cell apoptosis because of its electrons. Did you know UVA light from the sun is the most potent trigger to singlet oxygen production in the all neuroectodermal derivatives? Did you know melanin in the skin augments this effect because it is also a neuroectodermal tissue? I doubt you do because no centralized MD does.
Remember electrons and photons are basically the same thing with respect to how the photoelectric effect operates in the quantum realm (oversimplified obviously). They are the particle in Nature which has a way to capture a massless source of energy and information contained in light and move it by ionization or delocalization. This helps explains why all cells release ultraweak UV light. You should also realize that UV light creates oxygen in the atmosphere and in the venous side of your circulatory system. Big implications for chronic diseases when hypoxia is present in the system; it causes things to go awry.
Any replication stress then initiates the DNA damage response.
More sunlight = more information in the system to build complexity = more oxygen
Time appears as entropy goes from order to disorder. When entropy is controlled by a dissipative system, time can appear to be illusory.
This means that the less information you have about a data set in a cell, the higher its entropy must be in the system. Cells limit entropy by controlling their atomic arrangements. In precise terms, entropy is a measure of the number of possible atomic arrangements that a system of particles can be in.This is important in understanding how Nature engineered our biological clock gene to work.
Remember that stored energy in HEALTHY cells is coherent energy. The organism is, therefore, a highly coherent domain possessing a full range of coherence times and coherence volumes of energy storage. This keeps it far from equilibrium and makes it a highly dissipative system of organization to control entropy.
Reminder: Cellular organization is the key to precision optical signaling. Life is all about optimizing AMO physics INSIDE OF CELLS. It transforms energy from the environment to do this. Modern physics now has proven that energy and information are equivalent in physics. Landauer’s Principle of 1961 & Shannon’s 1948 work was critical in making this linkage. Modern quantum biology has experimentally proven that energy is trapped directly at the electronic level in cells. Energy is stored not only as vibrational and electronic bond energies in biochemicals, but also in the structure of the system: its enzyme kinetics, membranes, and in gradients, fields and flow patterns, compartments, organelles, cell water, and tissues. All this in turn enables organisms to mobilize their energies coherently at any time it is needed and hence make available the entire spectrum of stored energies for physiological work. It is energy on demand by atomic design.
SUMMARY
During his work with chemicals, Popp learned that 380 nanometers, the wavelength altered by carcinogens, is also the key wavelength that cells prefer to use to repair themselves. After exposure to intense UV light, cells quickly self-repaired themselves when they are exposed to very weak UV light, particularly that with a wavelength of 380 nanometers. Popp hypothesized that cancer results from a disruption of cells’ photo repair system. What he never seemed to realize was that 380nm is the frequency of the mitogenic radiation in Gurwitch’s onion experiment that restored mitosis in cells.
His hypothesis raised a question: what in the body produced this very weak light that powered the repair system? Popp and his student Bernard Ruth found that all living systems store light energy (photons) acquired from the sun and from plants consumed as food (photosynthesis), in DNA. This stored light is released as very weak, extremely coherent biophotons. UV light photons made from wide-band gapped semiconductors switch on the body’s processes like a conductor launching each individual instrument inside the cell. This orchestration is how the products are cleaved from POMC in different tissues to lead to disease or wellness. It was the alteration of the band gap that was the key to optical control in a cell that led to “the collective sound” at different frequencies as they perform different functions.
Over the years, Popp found that biophoton emissions from healthy humans display rhythmic patterns. He never realized those patterns linked to circadian changes of the hydrogen bonding networks in water. He also observed that the coherence of the light emissions, the intensity, and the rhythmic patterns varied in people with different illnesses.
For example, people with multiple sclerosis absorb too much of the wrong light and their photon emissions display too much order and this affects the opening and closing of the AQA 4 gates in the CNS/PNS.
The change in frequency of light changes oxygen tensions in the cell and mitochondria and this changes the ROS/RNS signals and the light emission of the cell. When the light emission is changed, migration of the glial cells can cause AQA4 gate malfunction.
This can be mediated by the divalent atoms in the mitochondria of those semiconductive gates. Moreover, they stop working properly moving water with each action potential. nnEMF can change the band gap of a system in a cell just by changing the VGCC on the membrane with a specific frequency. (see below)
The sun creates a different calcium signal in MS patients. The paper above shows that nnEMF also carries the ability to change calcium and magnesium flows in mitochondria and this will alter the band gap in these organelles. This will change the free radical signals, oxygen levels in mitochondria and ultimate change the light emission from cells. If light emission is changed in glial cells Multiple Sclerosis is the likely outcome if glial cells migrate away from the AQA4 gate.
Schwann cell precursors (SCPs) are glial progenitors, closely associated with developing nerves of the peripheral nervous system along which they migrate, sometimes long distances, throughout the body. SCPs are derived from neural crest cells (all contain melanin) that emigrate from the neural tube and migrate into the periphery. Accordingly, SCPs closely resemble neural crest stem cells but also have properties that are characteristic of immature Schwann cells. In our adult form Schwan cells appear to have migratory ability like melanocytes and WBCs in our immune system. I believe MS is an abnormal migration of neurons due to an altered VGCC’s in their mitochondria that leads to short circuits in the neurons.
ALS MIGHT ALSO BE A MIGRATORY NEURON DISEASES DUE TO A LOSS OF ENDOGENOUS UV SIGNALING
All spinal motor neurons derive from motor neuron progenitor cells, located in a restricted ventral region of the developing spinal cord.
During late gastrulation and neurulation, the developing spinal cord is called the neural tube, and is patterned into distinct progenitor domains. MNs are specified from progenitors in the ventral neural tube. Once specified, newly born MNs are further specified into columns, pools, and subtypes, forming a unique topography. From these columns and pools, axons reach out to their targets under varying guidance cues. All MNs are cholinergic cells which integrate with the motor control circuit, the sensory system, and their outlying targets to control movement. Given the growing importance of the MN–glia interaction in a number of neurodegenerative diseases it is important to know that the initial specification of oligodendrocyte precursor cells (OPCs) share a common progenitor with MNs. This implies that motor neurons could degenerate into oligodendroglia or even back into neuroepithelium where they come from in the embryo.
Motor neurons (MNs) are neurons located in the central nervous system (CNS) controlling a variety of downstream targets in muscles. There are two main types of MNs, (i) upper MNs that originate from the cerebral cortex and (ii) lower MNs that are located in the brainstem and spinal cord. This explains why some forms of ALS is worse than others.
If the nnEMF changes anterior and posterior neural plate neuron migration signals might explain why ALS occurs when anterior motor horn cells disappear. The anterior end of the neural tube will develop into the brain, and the posterior portion will become the spinal cord. The neural crest develops into peripheral structures. At this point, the early nervous system is a simple, hollow tube. It runs from the anterior end of the embryo to the posterior end.
In vertebrates, neuroepithelial cells give rise to the neural tube, which forms through two processes along the anterior-posterior (AP) axis. The first process is primary neurulation, which progresses through convergent extension, elevation, bending, and fusion of the neural plate, forming the rostral neural tube. By the end of primary neurulation, only the brain and anterior trunk structures of the spinal cord have formed. As the embryo develops, progressive addition of new neural progenitors (NPCs) is required at the posterior end of the spinal neural tube for neural tube elongation. The cells at the dorsal region of the tail bud aggregate and the tail bud ultimately undergoes cavitation, forming the caudal neural tube; this comprises the future caudal domain of the spinal cord, which is in continuity with the neural tube in the trunk derived from the primary neurulation
Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND) or Lou Gehrig’s disease, is a neurodegenerative disease that results in the progressive loss of motor neurons that control voluntary muscles in humans
Currently no one knows where these anterior horn cells go, but given the papers on Zebrafish out of Stonybrook University in New York I bet the motor horn cells have altered melanin biology in those cells and this leads to their migration somewhere else in the nervous system. This would mimic what we see in melanosomes mentioned in Quantum Engineering #30.
Why do I say this?
Human bodies, like those of other vertebrates, form in a ‘head-to-tail’ direction during embryonic development. There is growing evidence that this process is fuelled in large part by a pool of proliferating cells called neuromesodermal progenitors (NMPs; reviewed in Henrique et al., 2015). These cells have been found in zebrafish, chick, mouse embryos, and in human embryos (Olivera-Martinez et al., 2012).
Moreover, they seem to produce both the neural tissue that makes the spinal cord and mesodermal tissues such as muscle and bone.
Vertebrate embryos establish their primary body axis in a conserved progressive fashion from the anterior to the posterior. ALS is a disease that is linked only to anterior motor horn cells. During this process, a posteriorly localized neuromesodermal cell population called neuromesodermal progenitors (NMps) plays a critical role in contributing new cells to the spinal cord and mesoderm as the embryo elongates. Defects in neuromesodermal population development can cause severe disruptions to the formation of the body posterior to the head. Given their importance during development and their potential, some of which has already been realized, for revealing new methods of in vitro tissue generation, there is great interest in better understanding NMp biology.
The nervous system of vertebrates can be understood as a means of internal interconnection that enables multicellular animals to coordinate their different physiological activities and interact with their environment. ALS presents a seeming paradox to centralized healthcare because only
Zebrafish research at Stonybrook University by
thmic patterns. Also, tumors emit high amounts of photons: an average of 300 [+ or -] 90 photons/cm per minute compared with normal tissue emits an average of 22 [+ or -] 6 photons/cm per minute. Human cells that emit too much light seem to be a problem. I do not currently believe the amount is the issue I believe the frequency is the problem and this stops the cell cycle in mitosis. When this occurs oncogenesis begins.
Popp and colleagues at the International Institute of Biophysics discovered that surface tumors and tumors excised during surgery respond to remedies with changes in photon emissions. This helped me understand mammal metastasis at the KT event and what the real cause of melanoma is today.
Elisabeth Zieger, Michael Schubert. New Insights Into the Roles of Retinoic Acid Signaling in Nervous System Development and the Establishment of Neurotransmitter Systems. Int Rev Cell Mol Biol, pp.1-84, 2017. hal-02117372
Hydrogen = H+. Deuterium = D. . It is the atomic chameleon. It is the first element on the periodic table. It is what our sun is mostly made from and burns most to make energy. It is the element found in greatest density inside of a mitochondria. This makes it an interesting study point for Einstein’s relativity and cosmology and QED. Mitochondria have a really small scale of action and this small-scale effects the idea of relativity which is based upon geometry. Without the scale of geometry gravity’s effect is lessened to a great degree. Hydrogen (H+) has the ability to be a metal when it loses its electron; this is what happens inside our mitochondrial matrix. As H+ is can act a superconductor. Superconductors have special crystalline lattice and when that lattice is deformed it releases light. This makes it the focus of quantum electrodynamic theory. This means our mitochondria is filled with ionized plasma. This is very similar to what the sun does when it burns hydrogen. Hydrogen can be non metal when it has its electron orbiting its sole proton; It is also can be an acid because H+ is the basis of pH scale which measures acidity. Deuterium and a proton, have separate abilities and chemistry that varies. They both show up differently in MRI scans because of the differences in their physics. H+ and D interacts with water differently. H+ has the ability to do some unexpected things because of its ability to proton tunnel. The barrier for deuterium to tunnel is markedly reduced compared to H+. When we add infrared light H+ really become quite special. With 1538.5 nm photon frequency added to cell water, proton transfers in water are increased dramatically. This is called proton tunneling. This effect changes receptor biology and enzymes. Did you know every biologic enzyme known to man uses proton tunneling to work? All DNA and RNA only work when they are hydrated because they require hydrogen protons to tunnel!!! This makes hydrogen life’s magic weapon in enzyme and receptor actions. It has the same effect on DNA and RNA as well. Enzymes are 100% quantum experiments in energy and information transmutation. So how does hydrogen fit both Relativity and QED theory? Read on……………………..https://nautil.us/will-quantum-mechanics-swallow-relativity-235658/
The living universe selects for maximum entropy, and minimum waste heat.
The implications of this idea include:
The emergence of complexity: The universe’s drive for maximum entropy and minimum waste heat led to the melanin renovation Rx. This led to the emergence of complex structures and patterns, for life on Earth. Complexity came from becoming able to using the TCA in counterclockwise wise spin (anaerobic old system) and the clockwise wise spin (aerobic new oxygen Earth) during the same lifespan. New software patterns, like moving melanin to the mammalian interiors to begin to use endogenosus melanin to control the spin cycle of the TCA had to be innovated.
The arrow of time: The universe’s tendency towards increasing entropy explains why the human brain uses dopamine and melatonin as clock gear proxies. Both are critical in renovating all non visual photoreceptors in us. There use is why we perceive time as moving in a particular direction. Mammals’ criticality begins with UV light because it works with mtDNA, quantum dots, and melanin to create VUV-IR light inside a cell. When the critical amount of these entities goes missing inside mammals, they suffer a loss of healthspan or a loss of time.
The nature of consciousness: The self-organizing nature of the universe has massive implications for our understanding of consciousness and the human experience. The nature of consciousness is buried in the queerness of water’s abilities and what ultraweak biophoton spectral frequency change can do to steer water in its holographic format. Scientists at the US Department of Energy Oak Ridge National Laboratory (ORNL) have discovered new properties of water that go beyond the known laws of classical physics.
