How did we get creativity? Neanderthals migrated North got to 51st latitude froze started wearing animal skins and used fire inside caves and their brains shrunk as a result. As they shrunk due to dehydrated melanin sheets, melanin becomes dopamine. The dopamine built up and we got art culture and DaVinci.
2. Note how melanin degrades on the slide on the top line. It degrades into dopamine, other amines, and L-DOPA. When you undergo a TBI, as the Neanderthals did by going too far up on the planet, it gets cold, and you need animal skins and fire to keep you warm. Why? Neanderthals did not have uncoupled haplotypes yet. That is a human innovation to high-latitude living. As a result, they flood their shrinking brain with more dopamine than they should have had. Voila = You eventually get Michealangelo, DaVinci, and Rembrandt.
3. Look at the picture.
4.
5. Paying attention?
6. The Great Oxidation Event or Oxygen Holocaust is going on in every skull on Earth now due to nnEMF and blue ubiquitous use.
If you understand what I have laid out on my blogs over 20 years, all chronic diseases are photo-bioelectrical electrocution of the inside of a cell. Why? Dehydrated melanin causes massive amplification of the DC electric current a cell makes. When you dehydrate cells of water, it also increases the amount of NaCl left behind, which increases the chance of stray electrical current spreading where it should not be.
7. Remember what Nick Lane told us in his book, Power, Sex, and Suicide. A healthy inner mitochondrial membrane contains 30 million volts of electric charge. This charge would typically be devastating to a cell. It raised a big question when I read this fact long ago. How does a cell dampen the electrical charge? @MitoPsychoBio
Pure water containing no ions is an excellent insulator of electric charge. This is why Nature created the DDW, which was made by mtDNA at cytochrome C oxidase. What was the stimulus for her to gain this wisdom?
It was the wound of the Great Oxidation event. The toxic wound Nature sustained from the presence of oxygen and massive electrocution drove endosymbiotic growth or the merger of the two domains of life on Earth 650 million years ago. Nature would never have innovated mitochondria without photo-bioelectrocution as the wound. It was the stimulus that created eukaryotes.
8. What ruins this system? Ruin the water and increase stray electrical currents, and you get cancer.
FYI, when you add SV40 and LNPs together, in our modern world, it is the perfect soup for creating a turbo cancer.
Wake the fuck people.
MAHA = HAHA.
@threadreaderapp make a roll
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2. All one needs to know about the climate scam in one slide. Humans are the penultimate primate. We need more CO2 so plants make more 02 in our environment. Coupled oscillators, are C02 and 02 for the clade of silly talking monkeys.
The text in my slide below claims a "40-year hoax" and "CO₂ famine," arguing we need CO₂ at 1,200 ppm to avoid calamity, with humans as "penultimate primates" benefiting from more CO₂ for plant growth and thus more O₂.
This echoes decentralized climate views held by me: Earth has been in a relative CO₂ "famine" for millennia compared to geological highs, and rising CO₂ (now ~420 ppm as of 2025) has driven global greening, increased crop yields, and reduced famine risks.
For example, India's shift from famine-prone in the 1960s to agricultural exporter is partly attributed to CO₂ fertilization alongside green revolution tech. Some argue past low CO₂ contributed to events like the Carboniferous rainforest collapse or even the Permian extinction via "phytoplankton blackout."
Every single thing the government is behind is a bullshit story to enslave silly talking monkeys.
3. On CO₂ and O₂ coupling: Over geological scales, these two substance linked by a quantum process called photosynthesis and this process is not subjet to WEF induced government propaganda. Even a moron thrid grader knows that photosynthesis fixes CO₂ and releases O₂, while carbon burial raised O₂ in the past.
But today, O₂ (20.95%) is stable; human CO₂ emissions cause a tiny O₂ drop (~0.0001% per year), negligible for life.
More CO₂ boosts photosynthesis, potentially increasing local O₂ production, but not atmospheric levels meaningfully because our O₂ reservoirs are vast.
The key things that affect CCO water production are two paramagnetic substances. One from the GOE = NO that inhibits ATP, and the other oxygen that fueled the transition of primate to silly talking monkey. Oxygen and light were needed to sculpt that transition.
So why have I been traveling to the highest points on Earth and visiting many deserts along my path? A new blog covering it.
SPACE & EARTH ARE ENTANGLED AND LEAD YOU TO THE DISEASES Astronauts get. All Chronic diseases of man have the same etiology but few see it.
This blog starts at the magneto-heliosphere for the lesson and then I introduce you to an astronaut who has experienced this nnEMF in his own life so you can learn about your disease from his experience.
Learn the real ticket that moves the needle. If you want to know why your kid has childhood diseases and cancers I guarrantee you after this master class in quantum biology you'll know why.
We are the product of stardust that has burned us using oxygen. It light is the anvil which forged me which gave the will to make me formibile for my misfits because I will not break under force. All living things are electric and magnetic and they use the electromagnetic radiation of the sun and the earths magnetic field to create life. Man made radiation disrupts the natural order of atoms in our cells. The electromagnetic signals that come from the organization of these cells in mtDNA creates our health span or chronic diseases epidemics. This is plants and animals.
Humans are diurnal animals who need sunlight and darkness after sunset to function. This makes them fully decentralized. They cannot be optimal with too much of either. Indoor living, sun avoidance, constant exposure to artificial lights and man made electromagnetic radiation = a shifted metabolism from light that leads to all chronic diseases. Optimizing melatonin, dopamine, and melatonin (sunlight/darkness) and solar derived vitamin D, melanin, and NO is how you avoid chronic disease.
2. You don’t need more time.
You need more clarity in how you approach learning
Ask yourself 3 questions every morning:
1. What really matters most right now? 2. Who needs to hear from me today? 3. Am I living in alignment with what I say I value?
These 3 questions cut through the noise to get you to the signal of things that matter - at work, at home, in life.
3. Everyone tells you it is a story of red light..........when it is not when you have a chronic disease. It turns out that when you live in a world of nnEMF you need a lot of green light in your life for reasons few can explain. It is tied to your UPE signaling.
Even my astronaut has learned about this..........why haven't you?
If you think the Federal government is working for you you are an idiot. First they banned light bulbs that could help reduce oncogenesis. A peer-reviewed study showed that 734 nm near-infrared (NIR) can do this. Then the DOD, Fauci and Baric made a virus and jab designed to give you cancer. Then DARPA is supporting Gates research to block the sun at rhe same time they are inflating you money away as M2 rises. Every part of the government is involved in TIME THEFT.
Thomas Jefferson told us about clowns like this and in his time he told people to shoot the King over things way worse than what Americans are being force fed.
2. ^^^^^that was my second to last slide in the latest talk. This was another from the slide deck.
3. This was the last one.
"I am now convinced that centralized medicine built by Rockefeller money is actually philosophy. Astrology in our newspapers has more face validity than your profession does in 2025"
-----Dr. Jack Kruse
September 27, 2025
to a room filled with 679 Radiation Oncologists and radiation physicists.
What did the paper miss? Fasting makes them bigger.
Implications?
What happens to energy resistance in your ankle when you sprain it? It increases and it SWELLS because of energy loss.
What happens to energy resistance in the heart when it fails? IT increases in sizes and hypertropies because of energy loss.
What happens to a G class star like our sun when it it dies? It increases its energy resistance because it can no longer burn hydrogen and helium and burns all the elements to be come a red giant. It increases and becomes larger, because of this energy loss.
See the trend..........
What did the paper miss? Fasting causes mitochondria to get larger..........
It happens because of energy loss. The implications are vast for cell biology. Few.
I bet when @msahsorin gets better technology and can measure endogenous UPEs from these mitochondria it will show the UPEs spectra widens and becomes less coherent. Few.
@MitoPsychoBio
2. What happens in cells when UPEs output changes. Let us just look at one system to get a small picture of what light is capable of in information transfer? @msahsorin
3. When I take my doctors and patients on the deep dive of our circulatory system they enter the fascinating world of porphyrin spectra and unpack the Soret and Q bands. Let me unpack them in a way that’s clear and straightforward.
Porphyrins are these incredible, flat, ring-shaped molecules, think of them like nature’s own light-absorbing platforms, found in things like chlorophyll and heme. RBCs are loaded with porphyrins called hemoglobin.
These guys dying are just like the autism story is being sold by RFK Jr to give people breathing room. None of this is the truth. Everyone wants to blame one thing but it is a combination effect that assaults their colony of mitochondria slowly reducing the delta psi to cause electrical resistance in our semiconductive circuits to rise. This destroys the heat sink of metabolic water and directly alters information transfer in UPEs. It is obvious why this happens in decentralized medicine. It is shocking to the morons in centralized healthcare.
2. Number one cornerstone risk that raises energy resistance most is blue light and nnEMF that destroys the endogenous photolitholithograpghy biology needs to main entropy in the cell. Today biophysicists keep shitting the bed on what UPEs are. They are information qubits we use to stay healthy and alive and how they are controlled is the story of decentralized biology. Anyone who does not get this idea should be IGNORED.
“Previous studies showed that the plasma of a healthy individual contains up to 50,000 times more mitochondrial DNA than nuclear DNA,” said Dr. Alain Thierry, a researcher at the Montpellier Cancer Research Institute.
Biophysicists keep saying they do not know.........
Why do I know what it means? Because I understand what Shannon taught us about information. The uniqueness is the signal, not the noise.
3. Blood, specifically RBC are the cells that connect the sun to our mitochondria and major water supply in our arteries. So having optimized blood on your peripheral smear is a critical metric in mitochondrial methods. Your brain has more mitochondrial density than any other organ and this is no shock why it helps stave off dementia.
The parabiosis longevity RBC link = astrocytes loaded with Vitamin C = Belousov effect.
MANF (mesencephalic astrocyte-derived neurotrophic factor) is one of the factors responsible for rejuvenating the transfused older mice according to new research. Shocking no one who reads biophysics.
We know that MANF regulates metabolism and immune response in flies, mice, humans. what they forgot is that none of them can make their own Vitamin C either.......hence why the parabiosis effect is an RBC's effect.
The myopia of researchers amazes me.
The iron metabolism story is linked to poor RBC circadian function and will be critical for every physician to get down pat. The loss of iron movements in cells is linked to higher heteroplasmy levels. It will always link back to Vitamin A becoming weaponized to destroy the red light chromophores in the mitochondria. How does it happen? That is quite complex. A loss of the control of iron metabolism in humans will always smell like of a melanopsin dysfunction is because of how iron is handled in humans.
Heme/Onc MD's have been especially interested in systemic iron metabolism in the diseases they treat because iron is essential for red blood cells, where MOST of the human body's iron is contained. As most of you clinicians know already I believe all cancers are circadian disease linked to bad mitochondrial biology. So how is this all interconnected?
So when you know where most of the iron should be and where it should not be........you are lead to getting a deeper understanding of what controls heme synthesis and IRON. And that answer shocks small thinkers. The answer is the circadian biology of mitochondria.
Sunlight stimulates RBC creation and drives the flow of iron in your body so it too is a melanopsin issue related to the butterfly effect.
WHY?
Heme synthesis begins its first step in mitochondria. If you have a circadian mismatch disease tied to melanopsin dysfunction by definition you are blue light toxic or nnEMF toxic and this cause a defect in mitophagy and ruins the iron cycle in humans. This immediately affects the liver clocks too.
People in healthcare often forget heme synthesis occurs partly in the mitochondria and partly in the cytoplasm. This is exactly how the TCA and urea cycle are built in us too. The process begins in the mitochondria because one of the precursors is found only there. Since this reaction is regulated in part by the concentration of heme, the final step (which produces the heme) is also mitochondrial.
People with defects in iron always have a blood dyscrasia (anemia) at some level and it usually bleeds into fertility and thyroid hormone creation too because of its link to AM sunlight deficiency.
Remember purple light = UV light.
Purple light in sunlight stimulates RBC synthesis in humans. Blue light cause RBC's to break down sooner and live a shorter life than they can. What is the color of the main breakdown color of heme? It is the complementary yellow color, of bilirubin. Yellow is the complement of purple and orange is the complement of blue in the color wheel.
This is also why people with iron issues often have B12 and folate issues and most small thinker blame this on methylation problems but they forget that methylation is also a circadian controlled process. So.......most people with "RBC issues" also have methylation defects. Most functional medicine doctors brutalize this science. They have no idea how surface light controls it all.
The UV light is purple in the visible spectrum so anyone who is anemic and has ferritin issues is deficient in SOLAR redox at some level. We have to look for the connection as clinicians. It is always there.
This is also why B12 and folate absorption spectra are yellow too and are both linked to poor solar redox. Also, recall from Fritz Popp work every cell releases ELF-UV in a quantized fashion. People with bad redox always emit more UV than they absorb and they usually have iron metabolism issues that manifest in their blood.
This is why I wrote the recent patreon blog about looking at your peripheral blood smear to see if you are nnEMF toxic. Your blood cells are a big tell for me.
Once you know where the piece fits the story begins to make a lot of sense.......both quantum and common sense. #melanopsinwisdom 101.
People with iron issues also tend to develop other mitochondrial diseases like diabetes, cataracts, and Wilson's disease.
Photolysis of folate by the sun and its main serum form of 5-methylhydrofolate is BELIEVED TO be caused by UV radiation and by reactive oxygen species generated by UVA.
The problem with this theory advanced by Jablonski 15 years ago is that blue hazard induces the MOST ROS in the human skin, not UV radiation as this picture shows. Note when you get to the UVA blue light transition the BLH correction drops all the way to 0.100 and is DROPPING, not rising as we head into the UV range.
The reason for this is that blue light penetrates deep into the dermis where leptin and melanopsin are and UV light cannot do this. This was not well known in 2002 when she wrote her papers. It took me a while to figure all this out. newatlas.com/alkahest-young…
In 2019, I said I expected viral epidemics breakout in certain zip codes more significantly because viral infections react to the environment that is suboptimal. I also reminded my readers that these viral infections will cause rapid significant mitochondrial damage which in turn will liberate Vitamin A from opsins in cells and this puts downward pressure on endogenous production of Vitamin D. Then in September 2020, I said one thing is clear.........those who got C19 all had low levels of Vitamin D and immunodeficiency at some level that impacted their care and outcomes. This will affect their mitochondrial delta psi and lead to many other complications. I spoke about all those links here in this blog work. patreon.com/posts/22117599
TODAY IN 2025 I AM TELLING YOU IF YOU TOOK THE JAB AND HAVE A HIGH SPIKE PROTEIN ARRAY, YOU NEED TO MAXIMIZE THE VITAMIN D AND A cycles in your body and then the more controversial idea. If you are woman, even if you have infertility you should continue to try to become pregnant because there is a change the placenta from the pregnancy will retain the ability to clear a lot of the genetic damage from the jabs and limit intercalation. Let me be clear, the pregnancy will help you, it may not help the child so think about this before action.
The human placenta acts like plasmapharesis for DNA RNA and mtDNA damage. Few centralized MDs know this. My tribe does.
Recently scientists at the Wellcome Sanger Institute and the University of Cambridge conducted whole genome sequencing of 86 biopsies and 106 microdissections from 42 placentas, with samples taken from different areas of each organ.
The link between genetic aberrations in the placenta and birth outcomes has been established in the literature by this study but few MDs read outside their expertise, further studies using larger sample sizes could help to uncover the causes of complications and diseases that arise during pregnancy.
This study confirms for the first time in the PEER literature that the placenta is organized differently to every other human organ, and in fact resembles a patchwork of tumors collected from the circulatory system of Mother and fetus. The rates and patterns of genetic mutations were also incredibly high compared to other healthy human tissues.
The human placenta is akin to the ‘wild west’ of the human genome, completely different in its structure from any other healthy human tissue. It helps to protect humans from flaws in our genetic code, but equally there remains a high burden of disease associated with the placenta. This is why the DOD engineered spike protein to affect the uterus and hinder pregnancy creation. These findings now provide a rationale for my tribe for studying the association between genetic aberrations in the placenta and birth outcomes at the high resolution we deployed and at massive scale by the jab. I have been telling jabbed members who still bleed they should seek continuous pregnancy to rid their bodies of the genetic defects these bioweapons bring to people. No one knows how effective this information is but I guarrantee you no one is getting this information but my FARM members.
I encourage you to read the paper before deciding what to do. No one can legislate your sexual activity so having sex to get pregnant to save your life or improve it will not be interrupted by the state as yet.
The paper was fascinating because it allowed us to observe how such serious genetic flaws like a chromosomal copy number error could be ironed out by the baby tissues, but not by the placenta. the placenta seemed to be built to absorb all the genetic mistakes. I want to remind all my female savages that this is a way to lower heteroplasmy rate in your germ line eggs too. These errors would have been present in the fertilized egg. The paper showed us that derivative cell populations, and most importantly those that went on to form the child, had the correct number of copies of chromosome 10, whereas parts of the placenta failed to make this correction and it COLLECTED THE DEFECTS LIKE A FILTER. The placenta also provided a clue that the baby had inherited both copies of the chromosome from one parent, which can itself be associated with problems. Share this info with female savages who complied with tyranny.
2. Publication:
Tim H. H. Coorens, Thomas R. W. Oliver and Rashesh Sanghvi et al. (2021). Inherent mosaicism and extensive mutation of human placentas. Nature. DOI: 10.1038/s41586-021-03345-1
3. So the higher the spike is the more time you need to be pregnant with a placenta filtering the bioweapon debris. After each pregnancy sustained or not you need to assess your spike protein array and see how the number is trending and rinse and repeat. Make the placenta clean up your genome. Sorry men, still have not found a novel way like this to help you but you could volunteering to get the jabbed ladies pregnant. This is the first time I think that miscarriages might be a welcomed outcome.