In cancer, less is more if you add sunlight to your template. Fasting is the ideal way to create ketosis in oncogenesis. Using fats exogenously in foods is not the best choice in cancer, but not eating makes the body use its own fat sources to make CO2 and DDW in the matrix and changing the isotope fraction in the matrix BUT not the cytosol or plasma. That water created must then be placed into the sun to build the redox. Too many food and supplement guru's think ketosis is a food story when in cancer it is a FASTING story. The optimal way to do it is in sunlight. Why? Look at the picture below. Ketosis via fasting is a good complement to regular cancer therapy because it stimulates natural "electron restriction" through mitochondrion with poor ECT function. Cancer is a mitochondrial disease so fueling it with electrons from foods is not the most decisive. Stimulating mitophagy with fasting is what a mitochondriac would do as the first move. Moreover, fasting elicits different responses in normal and cancer cells because of heteroplasmy rate differential between both, and fasting can reduce certain side effects of cytotoxic therapy. I think ketosis from eating alone, with little to no AM solar light (UV-A and IR-A) provides not mitochondrial therapy in cancer. When you subtracting sunlight your cell remains busted. They remain without the ability to condense the respiratory proteins to lower heteroplasmy rates. If you do not do this, a high fat ketotic diet can drive problematic free radical signaling from our cytochromes and that can cause apoptosis. This is a problem tissue with a high mitochondrial density like the heart and brain. Cell suicide is OK in some places in the body but it is not OK in the heart or brain. This is why I am a believer in getting AM circadian biology signals right before using nutritional ketosis as an Rx. My fear today is that researchers like Dominic D'Agostino and Volek, Westerman are going to go full bore and use dietary ketosis over fasting in cancer because of what Dr. Seyfried has said and published by saying nutritional ketosis and fasting ketosis are equivalent. THEY ARE NOT because of free radical signaling. Free radical signaling is about the spin state of electrons, protons, and PHOTONS that mitochondria emit. FOOD gurus never mention any of this. Moreover, when their versions of ketotic studies are eventually done on people with heart and brain disorders people are going to shy away from ketosis because the data won't be good for outcomes longer-term in those diseases with high mitochondrial heteroplasmy. This is how a "half truth position" can lead us to a full lie clinical Rx. It can block us from the real truth. It is why light has to be fixed first to repair a ubiquitination problem in cancer cells. Ubiquitination defects are circadian defects that are fueled by mitochondrial heteroplasmy rates. The fuel source is INCAPABLE of doing it alone. Mitophagy is driven by solar light cycles and fasting best. Look at the picture below again. This is fundamentally what I have warned my own glioma patients about long ago. It's not that I do not want them to follow these researchers who advocate nutritional ketosis VERBATIM, it is more that I want him to think that they may not have thought this all the way through because none of them understand Dr. Doug Wallace’s ideas well enough about heteroplasmy rates and energy flows in mitochondria. Fasting is a better choice in cancer than a fat-laden diet. All light energy in excitons is transferred to electro-mechanical vibrational energy in mitochondria and the cytoplasm. That cytoplasm is supposed to be a field with water made by MITOCHONDRIA. In glioma patients, their cytoplasm is always deficient in water because of the redox shifted in mitochondria called the Warburg effect due to deficits in water creation from cytochrome C oxidase. My latest blog Reality 14 is all about the nuance of this shift. This is why the 100Hz vibration is linked to incident light waves interaction with cytosolic water made by mitochondria and not from the FOOD we eat. People forget in cancer state mitochondria cannot oscillate properly because of the pre-existing heteroplasmy is present. Dr. Doug Wallace and Megan McManus data are crystal clear on this. This process of energy transfer is a molecular resonance effect called internal conversion. When this process is broken you cannot burn fat and your mitochondria even if you eat it, and as a result, you do not make DD water or CO2 well for the matrix/cytosol. That created water is what becomes a battery for sunlight to create mitophagy via the fasting ketosis state so sunlight can be buried in it like a capacitor. That state lowers heteroplasmy and can be quite beneficial in cancer. My perspective as a person who treats glioma is very different than the LCHF food guru perspective espousing ONLY ketosis. It is one a tool and not a cure. Even fewer of them understand how created water inside the matrix/cytosol from mitochondria is essential to the redox potential of mitochondrial function to reverse the Warburg shift. You need too with this reasoning right here. That is why I am concerned about anyone who advocates ketosis from nutrition 24/7 and never mentions a thing about the light environment with fasting in glioma cases or heart disease. You must marry ketosis with AM UV-A and IR-A light to give ketosis a chance to work from the mitochondriac perspective. https://bmcmedicine.biomedcentral.com/.../s12916-017-0873-x

 

^^^^^^^^^How should calorie restriction be done? Not nutritional ketosis it is done via the sun. This is the Leptin Rx 101.

 

KETOSIS AND CANCER: You need to marry it with AM UV-A and IR-A light to make ketosis safe. Well with your cancer, using ketosis for this specific diagnosis first, is acceptable. But as you know I don’t like settling for acceptable. I want people to understand why different tissues have different rules of quantum engagement. Mitochondrial density and hardcore cell differentiation are one. In the brain, neurons are at their terminal pit stop from a stem cell transport. If you employ ketosis alone from exogenous fats and do nothing else what might this do to a brain tumor? It might cause de-differentiation. Guess what we neurosurgeons see in grade 1-3 gliomas all the time? DE-DIFFERENTIATION TO A GBM. That is my concern.........a food guru does not go this deep hence my concern for the unripe mind. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507492/?log$=activity

 

Ketosis adds massive amount of electrons and protons to the matrix. UV slows ECT down. You need both to get calorie restriction naturally.

What lowers the risk of glioma? Sunlight, not ketosis. See Pic.





Here is a ROUGH VITAMIN D CALCULATOR: https://fastrt.nilu.no/VitD-ez_quartMED.html

 

Check out my latest updated article: IS KETOSIS A CURE OR TOOL FOR A BROKEN MITOCHONDRIA? Stay true to yourself, engage with your followers, LEAD THEM, and ignore the food guru critics. Sheep are always looking for a new shepherd when the terrain gets rocky. Leaders show their character when followers begin to trust you. Innovative thinking distinguishes humans into leaders and followers.

https://www.linkedin.com/pulse/ketosis-cure-tool-broken-mitochondria-jack-kruse/