Oncology believes “bad genes” cause brain cancer: Implicit in this belief is the assumption that to get cancer or illness you must have a mutated gene. This is what we call genetic determinism. What they miss is that genetic expression is altered by the electromagnetic signals coming from RNA and DNA and the non-ionizing frequency EMF bands do change this information processing that occurs in the hydration shell around our nucleic acids. They are not studying this aspect of the cellular communication system because they do not understand the physics of biology. Nor are they studying how hydrated electrified proteins work normally, while dehydrated proteins have abnormal function because calcium levels and oxygen levels are altered and set the stage for brain cancer to occur.
Volkow and Achermann both showed definitively that brain physiology is changed by up-regulating glucose metabolism with respect to non native EMF. Both of their studies are the best we have in reference to this specific issue in the published literature. Brain tumors have risen 500% over the last 50 years and no one seems to know why. Our third researcher, Bissell, a breast cancer expert, has pointed the cancer causation gun squarely at an altered glucose metabolism. Bissell went back to the work of Otto Warburg to show us all just how deadly glucose can be in cancer. She has famously said, glucose metabolism in the presence of oxygen is not the consequence of the cancerous activity of malignant cells but is itself a cancerous event. Other researchers in neuroscience have pointed the smoking gun at the mitochondria in neuro-degeneration. These are diseases modern medicine has no answer for either. Could they be linked? Mitochondria are parts of our cell where food gets turned to electrons and water to protons. Mitochondria are basically small factories that normally pump out protons at a massive rate. These things do not happen in unison in brain tumor states. Within these protons is stored potential energy, and this potential energy is eventually transferred to water hydration shells around proteins and mitochondria throughout the entire cell. This potential energy is stored in the hydronium ion of the exclusion zone of water (EZ). The EZ is critical to cellular signaling in all life forms. When mitochondria make protons, water must be available to accept this energy package. If it is not, and mitochondria make too many protons, a positive charge builds up in and around the mitochondria because protons have a positive charge. A positive charge is acidic. This causes the local and surrounding pH to fall. This signal is read by the cell as rising inflammation, and the mitochondria response is to increase synthesis in ROS and/or RNS. These are the two signaling molecules that mitochondrial mainly use to ‘spread the word’ to other parts of the cell of how much ‘gasoline’ is in the gas tank to do cell work.
When that message gets muddled for any reason, we see problems develop at complex I of electron train transport chain (ECT). When failures occur here, an awful lot goes wrong in a cell. Most of this signaling chaos surrounding the basic mitochondrial information comes from literature on Parkinson’s disease or Alzheimer’s disease. These are diseases one gets before cancer usually develops but it shows the underlying problem at the mitochondrial and quantum level for all these diseases.
