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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
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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.
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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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