How You Rot & Rust
	pH, BUGS, & ROT. Understanding Biological Terrain When your body’s blood pH changes away from the ideal, it can become an environment for opportunistic microorganisms to grow and flourish. “Bugs in the blood” tell us the story of how we age, and how we ROT. That’s right, as we age, we rot. It is part of the disease process. It is the biological aspect of aging and disease. It is this rotting mechanism that helps to do us in and turn us back into the dust from which we came. There is a pH biochemical process which lies behind this rotting mechanism which I’ll discuss in a moment. But you should also be aware as we talk that this is not the whole story on aging and disease, for there is also an electrical/oxidative aspect. This is how we RUST. On the physical level, the aging and disease process is one of ROTTING AND RUSTING. Right now I’m going to talk about the rot, and I’ll discuss the rust later. The Biochemical Processes Behind pH Levels in Your Body. Let me talk very simplistically about the biochemical processes which lay the groundwork for the rotting processes in your body. This is the process of pH change and alteration down at the blood and tissue level. In order to do this in a simple fashion, let’s look at the process of food metabolism and how your body handles metabolic by-products from food intake. One of the by-products of food metabolism is CO2, carbon dioxide. As you know, lung respiration is one way in which your body eliminates carbon dioxide - it happens every time you exhale. However, in order to eliminate all of the carbon dioxide that is generated from normal metabolism, the lungs would need a respiration rate far above normal breathing. Holding this constantly accelerated rate would indeed be very difficult. Therefore, other mechanisms comes into play for handling the excess. 1) The CO2 combines with ammonia (produced from the oxidation of glutamine) and converts to urea in the liver and is excreted by the kidney. 2)The carbon dioxide combines with water through a process utilizing the enzyme carbonic anhydrase and the co-enzyme mineral ZINC. Through this process, carbonic acid is formed which breaks down into hydrogen and bicarbonate atoms/molecules. Aha - notice we just mentioned hydrogen. What does pH stand for??? Potential Hydrogen. When we talk about hydrogen, we are talking about potential ACIDS. When we talk of bicarbs, we are talking bases (alkaline substances). ACIDS are a normal by-product of metabolism. The body has the mechanisms in place to eliminate these acids. BUT, through poor dietary habits, shallow breathing, lack of excercise, toxicity exposures, etc., which can lead to liver stress and kidney malfunction, the ACIDS in the body do not always get eliminated as they should. In this case, what’s a body to do? Well if it can’t eliminate them, then it has to store them. And store them it does. When the body has an excess of acid it can’t get rid of, it gets stored for later removal. Where? In the interstitial spaces, also called the extracellular matrix - the spaces around the cells; the mesenchyme. When the body stores a hydrogen molecule/atom/proton (the acid) in the extracellular matrix, it believes that one day, the acid is going to be removed. Therefore, in order to be in balance, it knows that for every molecule of acid that gets stored in the tissues, an equal molecule of bicarb or base needs to be put into the blood because one day it will need to escort the acid out of the body. This is the body’s amazing compensatory mechanism at work. What we see here is the pH interplay between the blood and the tissues. If the body has an acid overload, it stores the acid in the tissues (the tissue pH decreases) and the blood compensates and becomes alkaline (the blood pH increases). Is this important? You bet it is. We are starting to scratch the surface for the rotting mechanism in our body. But before we get there, let’s push on and see what happens when the acids don’t get an opportunity to leave and more acid accumulates. The Acidic/Mineral Bugaboo
	As more acid accumulates in our body, it gets stored and pushed further, and ultimately it gets pushed into the cell. When it gets pushed into the cell, the first thing it does is displace POTASSIUM and then MAGNESIUM and then SODIUM. Wow. Those are three critical minerals in our body. The potassium and magnesium will leave the body, but as a preservation mechanism the sodium will be retained. Remember, the body knows it must place an alkaline molecule in the blood to escort out this increasing acid that is being stored in the tissues and cells. What it will often do (when mineral reserves are low which is often the case when eating a modern american diet) is draw CALCIUM (the most alkaline mineral known) from the bones and put it into the blood. This leads to something called free calcium excess. This is something you don't want and it is what's behind osteoporosis, arthritic pain, etc. It is brought about by the body compensating for an ever increasing tissue acidosis somewhere in the body. What you don't want to do in this case is take more calcium supplements. With that said, you can now understand why calcium is one of the most over-prescribed supplements. In these situations what the body really needs is more potassium, and magnesium, perhaps organic sodium, and possibly zinc which lends help to the whole proper acid breakdown process which we started five paragraphs ago. Let's push a little further. We have discussed four critical minerals:   - CALCIUM   - MAGNESIUM  - POTASSIUM  - SODIUM Well, wouldn't you know, these four minerals are the controlling minerals for our body's sympathetic and parasympathetic nervous system. Simply put, the sympathetic nervous system (SNS) controls our fight or flight response mechanism. The parasympathetic system (PSNS) controls our rest and digest response mechanism. It works like this: CALCIUM   Stimulatory mineral for the Sympathetic Nervous System MAGNESIUM Inhibitory mineral for the Sympathetic Nervous System POTASSIUM  Stimulatory mineral for the Parasympathetic Nervous System SODIUM  Inhibitory mineral for the Parasympathetic Nervous System When you run an acidic condition in the body, free calcium is in excess which stimulates the SNS, magnesium isn't around to offer a balance; potassium is depleted so the PSNS is not getting stimulated to offset the SNS and it is actually being further inhibited by sodium which the body is hanging onto with respect to the loss of potassium and magnesium. What does this give you? A person that is acidic, possibly prone to ranting and raving, hyperactive, quick to anger, moving too fast, burning out. Just what you'd expect from somebody running too acidic. And pushed to the extreme? You get a person that may appear as extreme PSNS dominant, i.e. lazy, lethargic, fatigued, but what you usually have is a person pushed beyond SNS dominance to outright exhaustion. According to some health care practitioners, it is rare to see a true PSNS dominant individual. Metabolic reality, compensatory mechanisms, and today's modern diet rarely allows for PSNS dominance. What we've just covered is a bit of the biochemistry that gets us to where we're going, and as you can see, it's one of the many fascinating inter-related pieces to this puzzle we call health. Now let's go further to build the picture. Acid/Base - Tissue/Blood - Biochemistry As acids accumulate in our body, they get stored and pushed into the tissues. Where they get pushed, on a local level, is going to be in large measure where in your body or with what organ you experience problems. When the body stores this excess acid, it will compensate and place an alkaline atom/molecule in the blood, and the blood will therefore become increasingly alkaline. Something interesting happens with the uptake of oxygen in blood with an overly alkaline environment. With rising alkalinity, blood can increase it's oxygen uptake, therefore the blood cells can hold more oxygen. Pretty good don't you think? Well, if you think so, your wrong. The reason is, a little bit of biochemical reality known as the Bohr effect. The Bohr effect states that with rising blood alkalinity, the red blood cells can saturate themselves with ever more oxygen. The problem is, they can't let go of it! If the blood cells can't let go of oxygen, then the oxygen isn't getting down to the other cells of the body. And do you recall what Otto Warburg discovered about cancer? It grows in an oxygen deficient environment. Now let's go further. We have alkaline blood due to the fact we have increasingly acidic tissue and/or cells occuring somewhere in our body. We have an alkaline blood which can't let go of it's oxygen to aerate an increasingly acidic environment. So get this ---- Here we have an Acidic environment with no oxygen. How can anything survive in this environment? Through anaerobic fermentation. What ferments anaerobically (i.e. without oxygen)? Yeast, mold and fungus. If that's the case, then this should bring up a most logical question; Since cancer thrives in an anaerobic environment, what is cancer? If you answered fermenting mold and fungus, you get a gold star. That is exactly what cancer is. Want proof? In 1903, Enderlein and Schmitt (Munich) cultured the fungus Mucor Racemosus Fresen from tumor cells. Other biologists (some of those mentioned earlier) have done the same. With access to a biology lab, you or any other scientist not beholden to political agendas can duplicate this experiment at any time. Why is this important? Because it is part of the story behind the aging, disease, and the rotting process which confirms what pleomorphic scientists have known all along about MICROBES, i.e. ALL microbes will change dependent upon their environment.
	When you age, get cancer, experience diseases, part of the process is that YOU ARE ROTTING ON THE INSIDE. This is a biological anaerobic fermentative process pushed into operation through the biochemical principles explained here. Most of these principles have been taught in one way or another to every medical student alive today. They just weren't shown how it works in practice. (By golly if they were shown that, with a little cognitive brain power they could figure out how to cure cancer. And that definitely is not good for the natural order of political academic hierarchy or long term industrial health care profits.) That as it is, let's talk about the ROT. And the rot, as it biologically culminates in the human body, begins with the microbe that at its beginning stages we have identified as the protit. Evolution of Microbes Before we look at the life cycle of the microbes in the blood, let's look at the evolution of microbes in general. I've already explained how a microbe begins its life as a colloid; a near spec of almost nothingness. Light into life. This will then evolve into a visible microbial particle that can be seen under the microscope (Anton Leuwenhoek's first experiment). These colloids are the building blocks of life. How they evolve is specifically a function of the terrain, the environment, or the medium in which they live or are cultured. As a microbe evolves, if you change its terrain or cultured environment, you'll see it going through various bacterial stages; i.e. round forms, rod shaped forms, even going into viral forms. Ultimately though, ALL microbes will see a FUNGAL CULMINATION. This fungal culmination can also be replaced by a YEAST CULMINATION. Biologists see microbes changing in the laboratory often, but for the most part dismiss it as contamination of their medium. The textbooks they learned from all held Pasteur's static ideas of "germs", and if something observed falls outside the standard textbook ideology, it is more often than not dismissed as laboratory contamination or aberration. Truth be told, it's usually the pleomorphic behavior that ALL microbial forms will exhibit if they are observed long enough and under the properly varying conditions. Which brings us to the blood. Microbes exist in the blood. If the blood terrain changes (i.e. pH etc.), the microbes will change their shape - bacterial - viral - yeast - fungus. Yep. There is a fungus among us, and it's in our blood. Give it the proper terrain (or more to the point improper terrain) and we get ROT. Part of the biological aging and disease process. This is why if you take a cancer tumor and culture it, you will get the fungus mucor racemosus fresen. Why that particular fungus? Because that is the species of plant based fungus that Professor Guenther Enderlein discovered has infected man and all mammalian species millennia ago! This is the Endobiont, the internal parasitic life with which we live. If health care biologists want a new road to explore for finding "cures" to today's diseases, all they need to do is adopt pleomorphic thinking and dig into Professor Enderlein's research.
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