Well, I'll say it once more, thanks Flux of the finger pointing at him on my answer to Jared's post on his recovery :
https://naturalfreedom.info/viewtopic.p ... 142#p50142
You mentioned Methylene Blue might be a psyop.
After a lot of reading (his
https://nutritiondetective.com/pages/ma ... -nutrition free book), and watching ten or so of his YT livestreams.
I gotta say, it's the most comprehensive, sourced and well thought out "theory" (as not accepted by peers, for obvious reasons) on Health, how we feed our chronic diseases because of what we eat.
His info :
https://nutritiondetective.com/
https://x.com/NutriDetect
https://www.youtube.com/@NutritionDetective
He focus on "over" types, as 95% of people are either overweight or this type
https://x.com/NutriDetect/status/1526202271251304448
Excess bodyfat is a body/genetic type that is good at storing toxins, creating storage space for them
Underweight people are NOT good at storing toxins away from the blood
Hence why underweight ppl actually die earlier than overweight people
Both situations involve toxicity
--
My operating theory is that underweight ppl are further along the liver/bile pathway damage spectrum
It's not as much the total amount of toxins as it is the speed at which one can excrete them
Theory: overweight ppl make more bile and can thus get rid of toxins faster
So, I ripped all his livestreams transcript, added his book and another one from Grant Genereux, and fed it to Notebooklm to ask questions.
Here's a very nice breakdown of his method :
General Principles for “Love Your Liver” Food Choices
The aim is to choose foods that support liver health by minimizing exposure to certain potentially problematic substances (Vitamin A, Copper, Manganese) while ensuring an adequate intake of essential nutrients and beneficial fiber. The approach is based on individual tolerance and simplicity.
Guiding principles:
1. Absolute priority: Very Low Vitamin A content (Retinol AND Carotenoids)
◦ Systematically avoid Vitamin A-rich foods: liver, whole/enriched dairy products, egg yolks, oily fish.
◦ Avoid highly colored fruits and vegetables (oranges, reds, yellows, dark greens): carrots, sweet potatoes, peppers, spinach, mangoes, etc.
◦ Prefer “white” or pale foods: white rice, white bread, white peeled potatoes, white mushrooms, white meat (chicken, turkey), certain lean white fish (if tolerated and not considered “fish” in the broad sense to be avoided).
◦ Acceptable fruits (if tolerated): apples and pears (peeled), bananas (yellow rather than brown).
2. Minimizing Copper and Manganese (Pragmatic Approach)
◦ The aim is to reduce overall intake, not to reach a precise numerical threshold.
◦ Avoid highly concentrated sources: liver, seafood, nuts, seeds, dark chocolate, dark tea.
◦ Recognize that some beneficial foods (legumes, whole grains) contain these minerals, but may be included depending on tolerance and their other benefits (see point 4 and 5).
3. Adequate Protein Intake
◦ Favor lean, well-tolerated protein sources: chicken/turkey fillet (preferably skinless), lean cuts of beef or bison (if tolerated), egg whites (occasionally, watch out for sulfur), and legumes (see point 5).
◦ Avoid pork (especially bacon) and processed meats.
4. Active search for Soluble Fibers
◦ Regularly incorporate sources of soluble fiber to help bind bile and potentially toxins.
◦ Preferred sources (if tolerated): oats (refined flakes or “rolled oats”), pearl barley, blond psyllium, pectin (peeled apples/pears), legumes (see point 5).
5 Reasoned inclusion of legumes (beans, lentils)
◦ Despite their copper and manganese content, legumes (particularly white beans, coral/yellow lentils) are often acceptable and even beneficial due to their richness in soluble fiber and resistant starch, and their low glycemic index.
◦ Their inclusion depends on individual tolerance.
◦ If canned, always rinse well to remove liquid.
◦ They can be a valuable source of protein and complex carbohydrates in this diet.
6. Listening to Individual Tolerance
◦ The most important principle: eat what is well tolerated. If a food causes symptoms, avoid it.
◦ Eating the same simple, well-tolerated foods regularly is acceptable and may even help identify sensitivities.
7. Moderation on Certain “Acceptable” Foods.
◦ Peeled white potatoes: ok, but avoid massive daily consumption due to glycoalkaloids (prefer 1-2 times/week or in moderate amounts).
◦ White rice: useful if high sensitivity, but beware of quality (arsenic) and potentially long-term glycemic impact if consumed as sole carbohydrate source. Rinse well before cooking.
8. Foods generally to be avoided or severely restricted
◦ Those already mentioned for Vit A, Cu, Mn (liver, seafood, nuts/seeds, colored vegetables, etc.).
◦ Dairy products (except potentially traces of fermented for probiotics if tolerated).
◦ Fish (mercury, Vit A interaction).
◦ Pork (especially bacon).
◦ Whole eggs (Vit A-rich yolk).
◦ Highly processed foods, added sugars, alcohol.
◦ Potentially: spicy foods, other solanaceae (peppers, tomatoes, eggplants) depending on tolerance.
9. Mineral support
◦ Ensure adequate intake of antagonistic or essential minerals often required: Zinc, Selenium, Molybdenum, Potassium (e.g. bananas, potatoes in moderation), Magnesium. Use good-quality salt.
In summary: Build your meals around well-tolerated lean proteins, pale carbohydrate sources and/or those rich in soluble fibre (white rice, oats, barley, tolerated legumes, potatoes in moderation), and a few peeled pale fruits if desired. Strictly avoid foods very rich in Vitamin A and concentrated sources of Copper/Manganese. Always listen to your body.
The basis of his research :
According to the sources provided, vitamin A toxicity and toxic bile are closely linked to a wide range of chronic diseases. Most chronic diseases today are considered to be directly or indirectly linked to vitamin A toxicity. The proposed underlying mechanism is often cholestasis, or liver damage, which causes bile to stagnate or leak into the bloodstream, affecting any part of the body where blood circulates.
Here's a list of the main diseases and chronic conditions mentioned in the sources as being associated with vitamin A toxicity and/or toxic bile/cholestasis:
- Autoimmune diseases, including autoimmune diabetes. Vitamin A toxicity is considered one of the absolute root causes of autoimmunity.
- Inflammatory bowel diseases (IBD). Isotretinoin (a form of vitamin A) has been associated with arthritis and IBD. Exposure to retinoids (vitamin A family) for the treatment of acne has been linked to the cause of IBD.
- Arthritis, mimicking rheumatoid arthritis and axial spondyloarthritis, induced by isotretinoin. Sacroiliitis is a classic symptom of Accutane (retinoid) toxicity.
- Liver problems. Chronic vitamin A consumption may be a significant cause of chronic liver disease. Vitamin A toxicity causes liver damage and cholestasis. Hepatic steatosis (fatty liver) is considered the hepatic manifestation of metabolic syndrome and a variation of long-term cholestasis. It can progress to cirrhosis and liver failure. Jaundice (icterus) is a sign of elevated bilirubin and potentially of cholestasis. Gallbladder problems and gallstones are linked to toxic bile.
- Kidney problems. Chronic kidney disease, kidney failure and kidney stones are mentioned. Bile in the blood can reach the kidneys.
- Cardiovascular disease. Sources suggest that hypervitaminosis A (vitamin A toxicity) may be a new risk factor for calcifying aortic valve disease. The role of beta-carotene and vitamin A in atherogenesis (development of blood vessel disease) is examined. Myocarditis has been mentioned as a possible effect related to liver injury and bile.
- Neurological and mental health problems. These include brain fog, memory problems, Alzheimer's disease, depression, anxiety, irritability, headaches, migraine, and idiopathic intracranial hypertension (high pressure inside the skull), a classic symptom of vitamin A toxicity. Retinoids and vitamin A are described as neurotoxic substances, capable of causing confusion, mental stupor and, in acute cases, altered behavior, polar psychosis (likened to schizophrenia).
- Eye diseases. Accumulation of retinaldehyde (a form of vitamin A) can cause eye disease. Vitamin A ruins the eyes. Eye problems are considered liver problems in Chinese medicine, with vitamin A causing both liver and eye problems. Xerophthalmia (dryness and degeneration of the eye) and keratomalacia are linked. Other symptoms include dry eyes, night blindness, visual disturbances, conjunctivitis and blurred vision.
- Skin and hair diseases. Problems include rashes, dry skin, desquamation, pruritus (itching), alopecia (hair loss), eczema and various skin disorders. Retinoic acid is described as a chemical peel that can dissolve cells.
- Gastrointestinal problems, including intestinal dysfunction, intestinal damage, leaky gut, constipation, diarrhea, nausea and vomiting. Pancreatitis may be caused by toxic bile moving up the pancreatic duct.
- Fatigue. Fatigue is one of the most common symptoms of chronic cholestasis.
- Anemia. Vitamin A toxicity can contribute to anemia by damaging red blood cells.
- Bone and calcium problems. Vitamin A toxicity can cause hypercalcemia (too much calcium in the blood) and contribute to tissue calcification. It can reduce bone mineral density (osteoporosis), leading to muscle and joint pain. Dental damage is also mentioned.
- Scurvy. One source indicates that vitamin A toxicity causes scurvy.
- Multiple sclerosis (MS). MS is reported as a side effect in people taking vitamin A.
- Metabolic syndrome, obesity and diabetes are also linked. Hepatic steatosis is the hepatic manifestation of metabolic syndrome.
- Thyroid problems (hypothyroidism).
- Respiratory diseases (bronchial asthma, persistent cough, shortness of breath). Bile in the blood can reach the lungs.
In summary, sources assert that vitamin A toxicity and toxic bile (cholestasis) are potential root causes or major contributing factors in a multitude of chronic diseases affecting various body systems.
And bonus for under types (I'm considering buying the program but for now, 200$ is too much) :
Here are the key principles of the approach, as described in the sources:
1. Reduce toxin intake: This is the most important first step. It involves avoiding or minimizing known toxic substances, even those often considered good.
2. Correct nutritional deficiencies: This is another pillar of the approach.
3. Promote elimination of toxic bile: True detoxification involves getting rid of toxic bile, which is the “poop of the liver”. This is done primarily through the intestine, where bile binds to substances and is then eliminated in the stool.
◦ Binding agents such as soluble fiber or charcoal can help bind bile in the intestine so that it can be excreted.
◦ Adjusting soluble fiber intake is mentioned as a strategy to help eliminate toxic bile.
4. Support bile duct repair and bile production:
◦ Substances like lactoferrin are mentioned as being able to help heal bile duct (cholangiocyte) damage and potentially increase bile production and excretion.
Why you should NOT go “as fast as possible”:
This is the most crucial point regarding your question about speed. Sources constantly warn against trying to speed up the process:
- Trying to detoxify too fast can release too many toxins (stored in the liver or fats) into the bloodstream.
- Bile itself is the most toxic substance produced by the body. When it leaks into the bloodstream (cholestasis), it is toxic.
- Pushing too much toxic bile at once can further damage the liver, bile ducts and intestine.
- This can bring back old symptoms (“detox setback”) and even create new ones, making you feel terrible, or even worsening your overall condition.
- The process of repairing and eliminating decades of poison is a marathon, not a sprint. It takes time.
- The speed has to be the “right speed”. You have to start slowly with interventions, especially for thin people who are very sensitive.
- Thin people (“under types”) are considered more sensitive, take longer to recover and require more care (“more care”). Their approach is distinctly different.
In summary, although the sources confirm your theory about the differences between “thin” and “overweight” types regarding liver damage, toxin management and bile production, the approach to repairing this damage is not to speed up the process. Instead, it emphasizes the need for a slow, careful and controlled process, focused on reducing incoming toxins, correcting deficiencies and safely eliminating toxic bile.
Specific details and individualization of this approach, especially for slim people, are available in the Love Your Liver program.
I'll keep this thread updated with my results starting in a couple of days as need to buy the necessary changes in diet / supplements.