Rasmus

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Rasmus

Rasmus

@RasmusPW

Roles in my life: son of a pathologist, engineer, FD, father, househusband, Hapkido trainer for kids - Now Rolfer, Osteopath, SE

Germany Katılım Ağustos 2021
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☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
Covered here: #post-370339" target="_blank" rel="nofollow noopener">forum.jackkruse.com/threads/long-h…
☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆@DrJackKruse

FYI: chewing mastic gum liberates D+ and that fixes the GERD that allows H Pylori to grow. People have no idea what mastication and bruxism is really about. Since magnetic fields need motion to operate and the KIE (Kinetic Isotope Effect) is the "atomic brake," then mechanical vibration is the literal jump-start for the human motor. When you introduce high-frequency mechanical "shaking," you are providing the kinetic energy necessary to overcome the viscous drag of deuterium (+). You are physically "knocking" the heavy water out of the liquid-crystal matrix of the dentin and the pancreatic duct cells. 1. Mastication as a "Vibrational Ignition" Chewing isn't just about breaking down food; it is a piezoelectric pump. The Trigeminal Pulse: Every bite sends a mechanical wave through the phased array of 32 teeth. This vibrates the stratified dentin, which generates a voltage spike. This clears deuterium in teeth and in the brain to close the LES and kill H.Pylori. Restarting the Clock: This "ping" travels via the trigeminal nerve to the thalamus. It acts as a mechanical "reset" for the MITF-AMPAR loop, clearing the "optical fog" and signaling the pancreas to begin the 2L bicarb "flush" of the day to get rid of deuterium the H. Pylori uses to cause Barrett's change and cancer. 2. Whole-Body Vibration (WBV) as "Isotopic Centrifugation" If the gastrocolic reflex and gastric emptying are stalled (as seen with GLP-1 drugs), the gut becomes a stagnant deuterium pool. Breaking the Surface Tension: Mechanical shaking (vibration) lowers the surface tension of the "heavy" water. This allows the melanin traps in the enterochromaffin cells to catch and fractionate the + more efficiently. The "Shake to Clear" Effect: Just like shaking a clogged pipe helps the sludge move, WBV forces the deuterium-laden "exhaust" toward the exocrine system (the "drain"). It restores the motion required for the magnetic grounding of the system.

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☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
FYI: chewing mastic gum liberates D+ and that fixes the GERD that allows H Pylori to grow. People have no idea what mastication and bruxism is really about. Since magnetic fields need motion to operate and the KIE (Kinetic Isotope Effect) is the "atomic brake," then mechanical vibration is the literal jump-start for the human motor. When you introduce high-frequency mechanical "shaking," you are providing the kinetic energy necessary to overcome the viscous drag of deuterium (+). You are physically "knocking" the heavy water out of the liquid-crystal matrix of the dentin and the pancreatic duct cells. 1. Mastication as a "Vibrational Ignition" Chewing isn't just about breaking down food; it is a piezoelectric pump. The Trigeminal Pulse: Every bite sends a mechanical wave through the phased array of 32 teeth. This vibrates the stratified dentin, which generates a voltage spike. This clears deuterium in teeth and in the brain to close the LES and kill H.Pylori. Restarting the Clock: This "ping" travels via the trigeminal nerve to the thalamus. It acts as a mechanical "reset" for the MITF-AMPAR loop, clearing the "optical fog" and signaling the pancreas to begin the 2L bicarb "flush" of the day to get rid of deuterium the H. Pylori uses to cause Barrett's change and cancer. 2. Whole-Body Vibration (WBV) as "Isotopic Centrifugation" If the gastrocolic reflex and gastric emptying are stalled (as seen with GLP-1 drugs), the gut becomes a stagnant deuterium pool. Breaking the Surface Tension: Mechanical shaking (vibration) lowers the surface tension of the "heavy" water. This allows the melanin traps in the enterochromaffin cells to catch and fractionate the + more efficiently. The "Shake to Clear" Effect: Just like shaking a clogged pipe helps the sludge move, WBV forces the deuterium-laden "exhaust" toward the exocrine system (the "drain"). It restores the motion required for the magnetic grounding of the system.
Alfred 🏄🏻‍♀️@HealthyAlfred

The bacteria responsible for most stomach cancer is in your stomach right now. You’ve never been tested for it. 4.4 BILLION people carry H. pylori. The WHO classifies it as a Group 1 carcinogen — same category as asbestos and cigarettes. That’s not an opinion. That’s the World Health Organization. Google it. It sits in your stomach lining. Silent. For years. Decades. Producing toxins linked to stomach cancer, ulcers, and neurodegeneration. No symptoms until the damage is done. Your doctor tested your cholesterol last year. Your blood pressure. Your blood sugar. Your thyroid. He never tested for the carcinogen living inside your gut. On a Greek island called Chios, people have been chewing a tree resin for 2,500 years. They didn’t know what H. pylori was. They just didn’t get stomach cancer. It’s called mastic gum. In human trials, it cleared H. pylori in 38% of patients. No antibiotics. No microbiome destruction. Published in the New England Journal of Medicine. 1g before breakfast. That’s it. Your doctor’s approach: wait until symptoms appear, then treat the cancer. Mastic gum: kill the bacteria that causes it before it starts. A Group 1 carcinogen is sitting in your stomach right now and the person you pay to protect your health has never once checked for it. I didn’t learn this from a doctor. That should terrify you.

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☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
How ignorant is Seyfried on biophysics of cancer? This clip proves my point. They took Nuclei from Cancerous cells and put them in the Cytoplasm of healthy cells and nothing happened. They then took the Nuclei from healthy cells and put them in cytoplasm from Cancerous cells and the nucleus and cell turned cancerous. Proof it is not "DNA" driving oncogenesis. No its deuterium and Seyfried still does not know it. This is the ultimate proof that the "parts list" (DNA) is not the "engine" (Cytoplasm/Mitochondria). Those nuclear transfer experiments, pioneered by McKinnell and later emphasized by Seyfried, completely dismantle the Somatic Mutation Theory of cancer. If you put a "broken" nucleus in "clean" water, the system runs fine. If you put a "clean" nucleus in "heavy" water, the system breaks. HE STILL DOESN'T SEE IT. 1. The Cytoplasm as the "Isotopic Sink" The cytoplasm is where the metabolic water lives. It is the fluid that surrounds the mitochondria and the nucleus. The "Heavy" Water: In a cancerous cell, the vagal exhaust and the bicarb loop have failed. The cytoplasm is saturated with 150 ppm deuterium silt. The "Weld": When you drop a healthy nucleus into that deuterated cytoplasm, the Kinetic Isotope Effect (KIE) takes over. The 𝐷−𝐶 bonds on the histones and methyl groups "freeze." The 𝑝53 "guardian" can no longer "slide" along the DNA to check for errors because the water lattice is too "stiff" (dielectric 78). The Result: The nucleus "turns cancerous" because it has been magnetically and kinetically locked by the isotopes in the water. 2. Why Seyfried is "Half-Right" Thomas Seyfried correctly identifies cancer as a mitochondrial metabolic disease, but as I've noted for 20 yrs, he misses the Isotopic Mechanic. Seyfried's View: It's about fermentation vs. respiration (the fuel). My Decentralized Mechanic's View: It's about Mass-Density. Fermentation is what happens when the mitochondria are so "silted up" with deuterium that they can no longer "spin" the ATP synthase at 9,000 RPM. The cell defaults to fermentation because it’s a "Low-Torque" Safe Mode. 3. The "Infinite Set" Connection Going back to my Cantor analogy on math and the sun: A Healthy Cytoplasm is an "Uncountable Set" of molecular degrees of freedom powered by the Sun. It has the "Infinities" required to keep deuterium in suspension. Cancerous Cytoplasm is a "Countable/Finite Set." It has lost its complexity (its dielectric constant). The "search space" has shrunk, making the genome vulnerable to the "coordinated attack" of 150 ppm deuterium. The Decentralized Mechanic's Conclusion: Oncogenesis is an "Isotopic Drowning" of the nucleus. The DNA isn't "mutating"; it's being physically crushed by the weight of the water it’s sitting in. Cancer = The 4th Ventricle Vortex stalled. The Cure = Re-establishing the Magnetic Vacuum to "exhale" the silt. Seyfried angers me with his ignorance.
☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 tweet media
Jamie Andrews@JamieAA_Again

They took Nuclei from Cancerous cells and put them in the Cytoplasm of healthy cells and nothing happened. They then took the Nuclei from healthy cells and put them in cytoplasm from Cancerous cells and the nucleus and cell turned cancerous. Proof it is not "DNA" driving oncogenesis.

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Moon Oh(吳文碩)
Moon Oh(吳文碩)@mkf6gpy·
Best article for DMSO here, For bladder cancer ,The oncologist do TURST and let the cancer make jungle inside the bladder for at least 3-4 months and recommend BCG or other chemotherapy to fall off the cancer or recommend another TURST again , For patients, suffering back pain and constipation and risk of transition to another organ because of gap between the surgery and chemotherapy, The DMSO taking orally can fall off the cancer before they grow big and deep if you believe or not , It is like you do chemotherapy yourself daily . ( it is not medical advice but personal experience )
Kate Shemirani@KateShemirani

The Miracle in the Shadows: DMSO and The Cancer Treatment They Tried to Bury By Kate Shemirani, 2025 Dimethyl Sulfoxide, or DMSO, is one of the most powerful, natural healing agents you've likely never heard of. Why? Because it threatens one of the most lucrative industries in the world, cancer treatment. With the ability to stop pain, reverse cellular damage, and destroy cancer, it was never going to be welcomed into the chemotherapy club. What Is DMSO? DMSO is a naturally occurring sulfur compound originally used as an industrial solvent. But it turned out to be one of the most promising medical treatments ever discovered, healing everything from burns, strokes, and autoimmune diseases to infections, organ damage, and cancer [(1)]. How Does It Help With Cancer? DMSO fights cancer in multiple ways: Reprogramming cancer cells: It forces cancer cells to differentiate, turning them back into normal cells instead of multiplying uncontrollably [(1)(2)]. Toxic to cancer, gentle to normal cells: It kills cancer cells without harming healthy ones [(1)(2)]. Boosts immune recognition: DMSO exposes hidden cancer cell markers, allowing your immune system to see and eliminate them [(1)(2)]. Supercharges treatments: It increases the effectiveness of natural and conventional anticancer agents and helps deliver them across the blood-brain barrier [(1)(2)]. Why Has It Been Suppressed? Despite hundreds of published studies, the FDA erased DMSO from mainstream medicine. Why? Because it can replace or dramatically reduce the need for chemotherapy, and over 65% of an oncologist’s income comes from chemo drugs [(1)]. You do the maths! How to Use DMSO Topically: Apply 70% DMSO gel or liquid directly to the skin over areas of concern. Orally: Start with a low dose, around 1 teaspoon (5ml) of 70% DMSO diluted in juice or distilled water once daily. Always use medical or pharmaceutical grade DMSO, and build up gradually [(1)(2)]. Intravenously (only under medical supervision): Used in trials and clinics to deliver DMSO directly to tumors or in combination with other agents [(1)]. ** Important: DMSO carries substances through the skin and into the bloodstream. Always clean the skin before application and avoid contact with toxins, creams, or perfumes. And My Final Word DMSO is not just another “alternative.” It is the alternative that could replace so much of modern toxic treatment, which is exactly why it was buried. But it’s back. And now, you can use what they tried to hide. I use it too. But I’m not telling you to do what I do, I’m telling you to do your own due diligence and make true Informed choices. References 1. A Midwestern Doctor, How DMSO Naturally Eliminates Cancers, April 2025. Mercola.com 2. A Midwestern Doctor, The Forgotten Side of Medicine, midwesterndoctor.com/p/dmso-transfo… 3. A Midwestern Doctor, Hundreds of Studies Show DMSO Transforms Cancer Cells, midwesterndoctor.com/p/hundreds-of-… Copyright Kate Shemirani, 2025 “Natural Nurse in a Toxic World”

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☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
DMSO is a polar, aprotic solvent that has a profound affinity for water. The Mechanism: When DMSO enters a "stiff" water lattice (dielectric 78), it disrupts the hydrogen-bond network of water. The deuterium Fractionation: By breaking these bonds, DMSO "loosens" the grip that 150 ppm deuterium has on the water lattice. It effectively acts as a "chemical centrifuge,"helping to "un-weld" the isotopic deuterium silt from the cell membranes and mitochondrial intermembrane space. pubmed.ncbi.nlm.nih.gov/17661513 DMSO is not chiral itself, but it acts as a Chiral Solvent Substitute that restores the Chiral Induced Spin Selectivity (CISS) in a "seized" lattice. In my decentralized framework, it isn't just a "pore maker", it is a lattice breaker in things made from water with a low dielectric constant. DMSO crosses the BBB effortlessly. This is why it is the ultimate" Decentralized Mechanic's Tool" for the 4th Ventricle Vortex.
OracleofTheMatrix@Oracle_ofMatrix

Hey Doc @DrJackKruse Why does DMSO work so well for so many ailments? I found a copy of the DMSO Handbook for Doctors a few years ago and I was amazed at how many treatments there are for various diseases and ailments in that book. Just curious what the biophysical mechanism is in DMSO that makes so effect on inflammation, burns, injuries, etc...?

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Dr Sam Soete
Dr Sam Soete@sam_soete·
BIOTIN & GLUCOSE METABOLISM (A PEATY VITAMIN?) This one isnt talked about much but biotin deficiency has been linked to impaired glucose tolerance, fasting hyperglycemia, and decreased glucose oxidation. The mechanism goes through glucokinase. Biotin deficiency inhibits liver glucokinase activity which is a key enzyme in glucose sensing and response. Without adequate glucokinase function the liver basically cant respond properly to incoming glucose. (this is a bit more downstream of what I believe is generally the main driver in rising blood glucose levels for most people) Biotin supplementation improves glucose tolerance. High doses reduce fasting glucose in type 2 diabetics (who werent responding to sulfonylurea treatment). So you're actually restoring a nutrient-dependent enzyme pathway rather than adding another pharmaceutical mechanism on top. But more importantly, biotin ALSO operates at the mitochondrial level. Biotin-dependent carboxylases in mitochondria are essential for producing the heme precursors. So ↓ biotin → ↓ heme precursors → ↓ complex IV → ↑ bottlenecks & mitochondrial ROS. This reduces TCA cycle flux, alters acetyl‑CoA handling, damages mitochondrial structure, and secondarily decreases electron transport chain activity and ATP synthesis. It is another example of why the conventional approach to diabetes (manage blood sugar with drugs) is incomplete imo. This approach leads to the "chronic & progressive" paradigm that most doctors sell to their patients. If part of the glucose intolerance is driven by a micronutrient deficiency in a cofactor that enables glucokinase as wel as improving oxidative phosphorylation, then fixing that deficiency addresses the problem at a completely different level than exogenous insulin ever could. Something to consider for anyone with stubborn glucose numbers that arent responding to teh usual interventions. Best food sources of biotin: - liver - eggs - sweet taters - nutritional yeast
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Dr Sam Soete
Dr Sam Soete@sam_soete·
If you are afraid of the sun you have been psyoped to an unimaginable degree. Sunlight is a gift. UVB = Vitamin D UVB = Testosterone UVB = Melanin UVB = β-Endorphins UVB = Analgesic UVB = Leptin Sensitivity UVB = Weight-Loss UVB = Anti-Viral & Anti-Bacterial UVA = Nitric Oxide = Blood Pressure Regulation IRA = Melatonin Production IRA = Photoprevention vs Sunburn IRA = Builds EZ Water IRA = Anti-inflammatory IRA = Builds Collagen Red Light = Mitochondrial Function Red Light = Reduces Blood Clotting Blue Light = Circadian Health (morning) Blue Light = Serotonin Production Blue Light = Adipose Regulation
Blaine Anderson@datingbyblaine

Matchmaking client, 38, 5’11, Orange County, newly minted surgeon, handsome, in-shape, and… Pale. Like, didn’t set foot outside his entire 7 year residency pale. He wants to date active women. He lives in Southern California. This is problematic. I tell him he needs to get a tan before we take his photos. He tells me he’s a doctor, and asks if I’ve heard of skin cancer. I tell him he’s a ghost, and ask if he wants a girlfriend. He’s agreed to walk outside shirtless 10 minutes a day until his photoshoot 🙃

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Elijah Krings
Elijah Krings@Elijahkrings·
No matter how good your Leaky Gut protocol is, if there is ongoing exposure to toxins, there will be no healing Downregulation of intestinal stem cell (ISCs) proliferation & differentiation, driven by inflammation, gut-dysbiosis, intestinal immune dysregulation, microbial endproducts, loss of paneth cell signaling will compromise healin long term In studies of mycotoxin injury, giving binders to remove the exposure upregulated ISC function & regeneration of the epithelial layer The same will go for antimicrobial protocols needed to fully get hold of the problem at hand, if the goal is long term solution of your problem, without over-reliance on supplements Below is a list of support tools for ISC function (not exhaustive):
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Dr Sam Soete
Dr Sam Soete@sam_soete·
Pomegranates are the best. We all know this. This thread will dive into why they are so good for your gut & mitochondria, and how you can leverage that to optimize your health. 🧵
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☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
Explanation for Rockefeller-trained MDs (the ones still teaching the membrane-pump model while your own textbooks’ own history proves it was falsified decades ago): The post you just read is not hyperbole. It is the precise diagnosis of why cancer, neurodegeneration, and metabolic disease remain “unsolved” after 70+ years of “more data, more pathways, more drugs.” The living cell is not a bag of salty water surrounded by a semi-permeable membrane with Na/K-ATPase pumps burning ATP to keep sodium out and potassium in. That model was experimentally falsified by 1962 using three independent lines of evidence, yet it remains in every textbook because the Flexner-era curriculum cannot survive without it. Now what nomind did not do.....is go beyond Ling. Ling was right but the science was not precise. This paper in 2025 explains why his post is accurate. The 2025 Nature Physics paper I'm linking here (nature.com/articles/s4156…) is the Rosetta Stone that translates the historical experiments into modern information thermodynamics. What Ling never realized is that biology is not fundamental, but physics is. It proves experimentally, in a real quantum many-body system, that adding information where it does not belong raises the Landauer cost and explodes entropy production. That is exactly what centralized Rockefeller medicine circus maximus plan has been doing for decades: piling more molecular detail, more genomics, more pathways onto a foundationally wrong first-principles model. The result is not progress, it is magnified entropy, more disease, and more Rockefeller fiat profit from the downstream patching. Some of us used Ling's idea to build the new system. Those people need to read that system to understand all the problems have been solved by decentralized science by Nature.
no.mind@the_no_mind

x.com/i/article/2013…

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Dr Sam Soete
Dr Sam Soete@sam_soete·
Great article. Another interesting relationship between the gut & lipids is that LDL participates in binding, transporting, and functionally neutralizing endotoxins like LPS. Still needs more resesrch imo but body may upregulate lipoprotein particles as a defence to increased levels of ciruclating endotoxins in gut hyperpermeability.
Dr Sam Soete tweet mediaDr Sam Soete tweet media
George Ferman@Helios_Movement

x.com/i/article/2036…

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☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
1. Why Neurons "Quickly" Export Oxidized Lipids Neurons are the primary "electrical wires" of the brain. They must maintain a high signal-to-noise ratio to function. The Deuterium Trap: Oxidized lipids are often "heavy." When lipids undergo oxidative damage, they frequently incorporate deuterium or lose their precise chiral "bend." Optical Interference: In my "antenna" model, these damaged lipids act like "carbon buildup" on a spark plug. They create inertial drag and disrupt the flow of light (biophotons) along the neural membranes. Immediate Offloading: Neurons cannot afford the metabolic "heat" of repairing these lipids in situ while trying to process information. They "dump" them into the cortex glia (the "dumpsters") to immediately clear the "line" for electrical signaling. 2. Why Sleep is the "Garbage Truck" Window The brain removes these lipids during sleep (behavioral inactivity) to avoid electrical crosstalk. The Bicarb/Isotope Reset: As we discussed, the bicarb loop and p53-mediated repair are high-energy processes. By shutting down sensory input (sleep), the brain can redirect its "photonic budget" to the peripheral immune cells (hemocytes/macrophages). Clearing the Deuterium: These immune cells act as the "deuterium exhaust." By "docking" to the glia and removing the oxidized lipids, they are physically removing the "heavy water" debris that has accumulated in the brain's CSF and lipid bilayers. The brain is SUPPOSED TO remove these lipids during sleep (behavioral inactivity) to avoid electrical crosstalk. When glylymphatic drainage is non functional due to the KIE of D+. The Bicarb/Isotope Reset: As we discussed, the bicarb loop and p53-mediated repair are high-energy processes. By shutting down sensory input (sleep), the brain can redirect its "photonic budget" to the peripheral immune cells (hemocytes/macrophages). Clearing the Deuterium: These immune cells act as the "deuterium exhaust." By "docking" to the glia and removing the oxidized lipids, they are physically removing the "heavy water" debris that has accumulated in the brain's CSF and lipid bilayers. Maintaining the Lagrangian: If this trash isn't taken out daily, the buildup of acetyl-CoA and acetylated proteins (as mentioned in the paper) occurs. This leads to mitochondrial dysregulation (low 𝑁𝐴𝐷+) because the "heavy" lipids interfere with the construction of Cytochrome C Oxidase (CCO). 3. The Addiction Link: The "Overflowing Dumpster" In a state of addiction (or constant technology use), the "waking" period is unnaturally extended and the "antenna" is overstimulated. The Result: The neurons dump lipids faster than the "garbage trucks" (immune cells) can remove them. The Collapse: The brain's "dumpsters" (glia) overflow. The inertial drag in the CSF becomes permanent. The Craving: The brain senses this "clogged" state, this loss of optical coherence, as the "heavy" feeling of withdrawal. It then seeks opiates or alcohol to artificially thin the "sludge" or dampen the "noise" created by these uncleared, deuterated lipids. This study proves that peripheral blood cells are a critical part of the brain's "optical cooling system." Without them, the high-p53 human brain literally "overheats" from its own metabolic trash. Does Nick see it yet, Savages? Inquiring minds will want to assess this..........
Nick Jikomes@trikomes

During sleep, immune cells in flies migrate to the brain and "dock" to glial cells, which are holding sacs of oxidized lipids that were quickly offloaded by neurons during periods of waking. Those immune cells then "take out the trash," removing oxidized lipids from the brain, sort of like garbage trucks periodically coming to empty dumpsters placed outside of buildings. Why would neurons "want" to quickly export oxidized lipids? Why would the brain "want" to remove those oxidized lipids on a daily basis, during periods of behavioral inactivity?

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Benjamin Bikman
Benjamin Bikman@BenBikmanPhD·
I wonder how much of medicine is driven by drugs. For example, why did they decide that LDL cholesterol is the main marker for heart disease, rather than triglycerides or insulin? After all, triglycerides and insulin are better markers of heart disease risk. The reason? Probably because LDL cholesterol is "targetable"--there's a drug (statins) that will lower it. So it matters less that LDL is a good marker, and more that it's a number we can change with a drug. And of course, make money in the process. If there were a drug that lowered triglycerides really well, I suspect mainstream medicine would focus more on triglycerides. (Incidentally, the best way to lower triglycerides and insulin is to control consumption of refined carbohydrates.)
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Dr Sam Soete
Dr Sam Soete@sam_soete·
Thiamine (amoung other things) restores atp production in the hypothalamus which is the abundance signal the brain looks for to increase whple body metabolic rate which is commicated to the body via thyroid hormone. Thiamine is a critical cofactor for ATP production. Without adequate thiamine, oxidative phosphorylation is bottlenecked caus8ng ATP to fall and the AMP:ATP ratio rises (especially in one of the most metabolically sensitive structures in the brain - the hypothalamus). This shift activates AMPK (essentially an energy-sensing enzyme). It responds to AMP accumulation/ratio with ATP. In the paraventricular nucleus, active AMPK will suppress TRH release, which reduces TSH output and blunts downstream thyroid hormone production. Restoring thiamine status will therefore restore oxidative flux, rebalance the AMP:ATP ratio, reduces hypothalamic AMPK activity, and allows TRH to be released normally. It communicates abundance to the rest of the body via thyroid hormone. Functional thiamine insufficiency impairs PDH and TCA flux causing ATP to drop. AMPK activates and TRH is suppressed, and you get a centrally driven hypothyroid picture. This is different from primary thyroid issues and won't show up as an elevated TSH. It's one reason why a client can have classic low-thyroid symptoms with a supposedly normal TSH panel.
Elliot Overton@EO_Nutrition

Thiamine is basically the vitamin-equivalent of Thyroid Hormone: - Abundant thiamine = High metabolism - Low thiamine = Slow metabolism - Thiamine supplementation prevents obesity in animals by increasing thermogenesis - Animals low in thiamine have low body temperature and many signs of hypothyroidism - Reduced thiamine is associated with higher body fat % - Low thiamine causes a reduction in core body temperature - In obesity, fat cells express less thiamine transporters. These transporters increase with weight loss - Thiamine-dependent enzymes are reprogrammed in hibernation and govern reduced rate of energy metabolism. - In perch fish, high thiamine content in spring, highest in summer, and decreased to the lowest point in autumn/winter - In hibernating mammals, thiamine (and its associated pathways) are higher in the active phase and low during hibernation - Salmon in late fall/winter have high PUFA in muscle and lower thiamine. Whereas In summer, high saturated fats, higher thiamine and higher metabolic rate

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Jack
Jack@jack_schroder_·
We know the negative effects around sunglasses and sunscreen that destroy the fidelity of the energetics, timing, and signalling within your skin and eyes — and how these organs communicate into deeper tissues of the body like the nervous system, gut microbiome, liver, kidney, heart, gonads, etc. to dictate internal biochemistry via information from the external environment. When you block UVA/UVB light from sunglasses and sunscreen, you block vital wavelengths that help support this internal biochemistry, providing the light that helps repair, signal, and heal our bodies when in synergism with other colours of the rainbow, including infrared. Light interacts with chromophores on our eyes, skin, adipose tissue, and blood vessels to act like a communicator of the world that surrounds us. The energy, signalling, and timing that encompasses biophysics — which drives biochemistry — is also determined by the temperature we expose ourselves to, the food that we eat, the darkness we receive, the magnetic fields of the Earth, the people that we surround ourselves with, the situations we put ourselves in, and the senses that we feel (eg., sound, touch, smell). This language is communicated through light in the form of biophotons (UPEs), magnetochemicals in the form of free radicals (ROS/RNS), and through specialized molecular vibrations via phonons/solitons — these all ripple through our semiconductive network (eg., water, melanin, collagen, myelin) that interact with mitochondrial and cell biology. Contacts intervene in every biochemical pathway that sunglasses do, but with additional layers — hypoxia, mechanical friction, nutrient supply, biofilm formation, and direct interference with the lacrimal reflex. The cornea receives oxygen directly from the air rather than blood vessels to maintain perfect clarity for vision/circadian entrainment. It also relies on parasympathetic-induced tear secretions that provide moisture, nutrients, oxygen, and antimicrobial peptides/immunoglobulins to provide a healthy corneal layer. If you wear contacts you've blocked all of the above so your eyes start to atrophy and you lose energy, signalling, and timing in your tissues, leading to basically all forms of disease.
Jack tweet mediaJack tweet mediaJack tweet mediaJack tweet media
Jack@jack_schroder_

Contact lenses are worse than sunglasses for your health. You block UVA/UVB light, scatter IR light and convert it into unusable heat instead of mitochondrial respiration, prevent atmospheric oxygen absorption, and block tear film formation (provides oxygen, nutrients, antimicrobial peptides, immunoglobulins — essential for preventing infection and optimizing the turnover of this layer). This makes the cornea hypoxic and prevents the proper bending of light hitting matter — which enables you to convert it into electricity to drive biochemistry in all of your tissues via circadian entrainment to the hypothalamus and frontal lobes. These regions control your hormones, neurotransmitters, mood/emotions, thoughts, digestion, immune function, detoxification, reproduction, metabolic function, and more. The solution is to use narrow glasses as much as possible, whilst you optimize your health and eyesight in the meantime.

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☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
2. What is the difference between a rigid scoliosis case and a non rigid one? The amount of deuterium in the spine. More D+ in the spine the higher the kinetic isotope effect. When I did these cases I always used HGT to assess the KIE before I began. Nothing deuterium depletes a spine like the sun.
☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 tweet media☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 tweet media
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☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
Doctors use halo-gravity traction (HGT) as a safe, preoperative method to gently stretch and partially straighten the spine in children with severe or rigid scoliosis. While HGT does not permanently "repair" or fix the curve on its own, it serves as a critical first step to prepare the body for a more definitive surgical procedure, such as spinal fusion.
Brian Roemmele@BrianRoemmele

Doctor fixed A severe Scoliosis with Halo gravity traction method in children's (straighten the spine).

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☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆
Meat did not erase it. Deuterium collection is behind AD etiology. Limiting deuterium by any means necessary in the brain lowers the risk of IMJ damage. Nothing deuterium depletes more than the sun. So how much does Lufkin really know about APOE4, the sun and haplotype and how they link to AD? Not much. Might the human Transdermal Neuro-Optic linking MITF-AMPAR loop in neuroectorderm be how haplotypes came to be as an unfolding due to photo-bio electric resistance? It would seem to me Familial hypercholestemia would be a step in the direction of alteration of coupling efficiency from high to low latitudes after ancestors left Africa only to return to the Tropics? It explains APOe4 biology well. How? I'm describing haplotypes not as random mutations, but as adaptive biological "impedance matchers" designed to maintain the MITF-AMPAR-melanin coupling efficiency as humans moved across different solar "voltages" (latitudes). If the brain is a quantum computer, the haplotype is the "hardware revision" required to keep the OS (metabolism) running on a changing power supply. 1. Haplotypes as "Photo-Bioelectric Resistance" In Africa (High Voltage/High UV), the system required "high resistance" (high melanin/low vitamin D synthesis) to prevent photo-oxidation of folate and neurotransmitters. The Transition: As ancestors moved to high latitudes (Low Voltage), the "resistance" had to drop. Haplotypes emerged to downregulate melanin(freeing up UV for the MITF-SIRT1-NAD+ "ignition") and upregulate the AMPAR "gain" to capture the weaker metabolic signal. The Unfolding: This "unfolding" isn't just about skin color; it's about the Mitochondrial Haplotype (mtDNA) adjusting the coupling efficiency of the Electron Transport Chain (ETC) to handle different IR/UV ratios. 2. Familial Hypercholesterolemia (FH): The "Battery Leak" My link to Familial Hypercholesterolemia (FH) is the "smoking gun" for this theory. Cholesterol as a UV-Resonator: Cholesterol is the precursor to Vitamin D (via UV-B) and a critical component of the Exclusion Zone (EZ) waterinterface in the IMM. The Adaptation: FH (high LDL) may have been a Northern Haplotype's attempt to "buffer" more light or provide more substrate for Vitamin D/Hormone synthesis in a low-UV environment. The Tropical Return: When an FH-haplotype (designed for low light/high resistance) returns to the Tropics (High UV), the "coupling efficiency" is mismatched. The high cholesterol "over-collects" UV energy, creating thermal expansion (entropy) instead of coherence. This "shorts out" the MITF-AMPAR loop. This stimulus wil push cholesterol levels down in the Tropics pretty fast. If it did not react fast this would lead to the mitochondrial collapse and premature cognitive decline (dementia) seen in mismatched populations. 3. Implications for Disease: The "Latitude Mismatch" Dementia as an "Impedance Mismatch": If a "Northern" brain (high-gain AMPARs) is placed in a "Southern" light environment (or vice versa), the GDF-15 "stress flare" is triggered because the internal "UV-UPE" circuit is receiving the wrong "frequency." Topological Short-Circuit: This mismatch dissolves the topological insulator (the melanin-EZ interface). The cytoskeleton collapses not because it's "broken," but because the biophotonic "instruction set" from the haplotype doesn't match the ambient "solar voltage." 4. The "Transdermal" Cure This implies that we can’t treat "dementia" or "FH" as purely chemical issues. They are frequency-matching issues. Rewiring the Brain: We can use the skin's dermatomes to provide the specific "missing" frequencies (like IR-A volume or 380nm ignition) to "re-tune" the haplotype's resistance. The Goal: Restoring the -200mV EZ battery by providing the exact "photo-bioelectric" load the specific haplotype evolved for. This is why I think ApoE4, which is often called the "Alzheimer's gene", is actually just the ultimate "ancestral high-voltage haplotype" that now "short-circuits" when exposed to the flickering LEDs and nnEMF of the modern world.
☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 tweet media☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 tweet media☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 tweet media☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 tweet media
Robert Lufkin MD@robertlufkinmd

As a medical school professor, I teach about APOE4 -- the gene that makes you 2.5x more likely to develop Alzheimer's. We've told patients there's nothing they can do about it. A new JAMA Network Open study of 2,157 adults just proved us wrong. Higher meat consumption completely abolished the APOE4 dementia risk. The data: -> APOE4 carriers with highest meat intake: 55% lower dementia risk -> Their typical 2.5x excess Alzheimer's risk? Gone entirely -> Cognitive decline reversed: +0.32 standard deviations over 10 years -> Unprocessed meat was protective; processed meat was harmful regardless of genotype Researchers propose APOE4 is an evolutionary adaptation to meat-rich diets. The gene isn't a defect -- we just stopped feeding it correctly. This is personalized metabolic medicine. Your genes load the gun, but your diet pulls the trigger -- or puts the safety back on. Full breakdown coming on the Health Longevity Secrets podcast. Source: jamanetwork.com/journals/jaman… #APOE4 #Alzheimers #MetabolicHealth #Nutrition #HealthLongevity

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