cell division.
The above conditions further obstruct cell metabolism. When transmembrane potential
drops below 15 mvolts, it leads to cell division and eventually causes cells
to over populate. This enhances and diffuses the existing energy crisis from
the cells to the system. The energy crisis is then extended and generalized
for the system as a whole with the characteristic of low energy and low metabolism
for the system itself. We may say, that cells with low energy get into a “panic”
state of feverish multiplication in order to preserve their species, following
an inherent program encoded in the most fundamental part - their DNA, for survival
under the emergency of severe conditions. More cells are produced inside the
tumor, or more cells are produced adjacent to the tumor which found naturally
in a low energy or impoverished environment, diffused from the expanding prime
energy crisis – the prime cancer. Newer cancer cells will lack even more energy
for the same reasons. So, we see naturally why the tumor grows or diffuses to
adjacent areas and tissues, a phenomenon known as “cancer diffusion”,
i.e., cancers ability to diffuse to adjacent healthy cells and tissues which
is particularly unexplained today by medicine. Obviously, the more those
“low energy” cells multiply, more energy is needed in the organism as a whole
to feed the newborn cells. Therefore, the energy crisis and the cell starvation
continually expand, as does cancer.
The organism soon becomes a “poor society in a panic crisis situation” as a
whole, lacking even more energy. In such a case, more and more cells will be
in a “panic state” for nutrition and energy and so, we see that cancer triumphantly
metastasizes and generalizes. The organism or person becomes thin, weak and
underweight, with the common characteristic of loss of weight, low energy, and
low nutrition intake. Cancer then spreads and generalizes, with no way for
the organism or person to overcome this increasing need of energy and
nutrition.
Apparently, there is no way out of this “energy crisis” when many more
new cells appear, and the organism (or the person) dies. This is more or less
the macroscopic “scenario” of the cancer phenomenon. This is of course omitting
numerous details of the cell physiology, and the details of how the organism
gradually fails as a whole. The reason for this is “over population of starving
cells” and the resulting expansion of this “energy crisis”.
As an indisputable example and confirmation of the above, we may consider the
modern technique of cloning living cells through genetic engineering. The
technique of cloning living cells consists of forcing a newly fertilized cell
(egg) to duplicate into more copies so that one identical embryo develops. This
technique simply reported in the mass media consists of isolating a newly fertilized
egg and placing it in an environment of very low nutrition. This state of starvation
and obviously low energy causes it to divide into copies in exact agreement
to the ideas expressed above.
After a number of divisions into cell copies, biologists then remove the cell
copies and place them in an environment of proper nutrition and energy, where
an independent and self organized embryo develops.
The same technique for plants has been known for many thousands of years to
farmers for plants, called “meristomatic” culturing, or plant cloning as we
could say today. The description of this old technique can be found in encyclopedias.
A typical example (suggested to find and read) for meristomatic culturing or
“cloning for the plants” can be found in relevant books and encyclopedias for
Orchids, directly confirming our above hypothesis of multiplication and cancer.
Say you cut a small part of the leaf of the orchid and move it to a dry, isolated
air sealed environment. It is then placed on a dry inorganic material such as
stonewool (used in the building industry for sound insulation). Stonewool has
nothing to offer to the piece of leaf from the orchid. It only holds the leaf
mechanically in this air sealed environment. Being found in a “stressed environment”
without any nutrition, the cells in the leaf multiply and form a new born orchid.
The orchid is then moved into an environment where proper nutrition is given
to the plant for its future survival.
The secrets of life revealed by the phenomenon of Meristomatic Culturing
-Cloning for plants – known by farmers for thousands of years now – see major
encyclopedias.
Small pieces, cut from an orchid leaf, are placed in a closed bottle on a
wool stone, where the orchid cells are seriously nutritionally starved, away
from the mother plant. The cells, in order to survive, multiply and produce
a new orchid. Then the new developed plants, after the nutritional stress,
are transported to a normal nutritional culture where they further develop
to new plants. Modern cloning for animals is initiated by a similar nutritional
stress. We suggest “cloning meristomatic culturing” and “cancer”, all three
based in cell division and multiplication, have a starting phase of nutritional
poverty and stress or a forced low metabolism.
However, we may immediately question the following: Why orchid cells when stressed
lead to a new orchid and not to cancer?
Similarly, the other way around: Why cells in a body when stressed lead to cancer
and not to a new plant or animal like in meristomatic culturing or in biological
cloning?
The answer is that meristomatic culturing or biological cloning is always processed
away from the main plant or animal. A new identical plant or animal is developed
according to its DNA description of the cell and regardless of its location.
On a particular location or anatomic position of an organism, cells differentiate,
or specialize, or restrict their DNA function to a specific task according to
the location. This DNA restriction imposed by the anatomic position of the organism
is what prohibits a multiplying cell in the organism to develop into a new independent
organism as it would have done away from it and away from the particular anatomic
position. The position directs the new born cells to differentiate according
to a plan specifying the task of that position.
When starving conditions are imposed on an anatomic position of a plant or on
an animal, either the cells will die or the cells with the “DNA restricted by
this position” will produce a “monster form” multiplication that we call cancer.
It is beyond the scope of this article to discuss and prove the “form giving”
or “cell differentiation” factor on an anatomic position of an organism. For
the present scope, we may only call the controlling factor, the etheric archetype
or morphogenic ether associated with the organism, after Aristoteles who
specifically defines the non material and non visible “Ether” or the “Fifth
Essence”, as the non material agent that gives form to inorganic and organic
matter. Additionally, we may say that the etheric archetype universally
seems to be in operation in giving forms to plants, animals, stones, clouds,
mountains, the visible craters of the moon, the recent (late 90’s) found galaxy
arrangement in lines in the Universe, forms associated with cohesion forces,
forms of the iris of the eye, forms in crystals, ores concentration, forms in
dried water, dried blood, dried saline, ice, all different forms of the very
well known, but still unexplained, snow flakes!... etc. (suggested typical reference
for water formations: “Messages from Water” by Masaru Emoto, MD, Hado Kyoikusha
Co., Tokyo, Japan, ISBN4-939098-00-1, http://www.hado.com
Cancer also certainly has a form. Though, cancer is considered as a non controlled
multiplication of cells. We may directly say this is an exaggeration because
cancer is indeed the opposite. It is a controlled multiplication in a particular
volume. Any arbitrary accumulation of cancer cells in a particular volume is
subject to immediate fatality, as the necessary metabolism is not supported.
For any cells, including cancer cells, an elementary system providing nutrients
and sustaining at least an elementary metabolism is required. Tumors are known
to create an organized net of capillary tubes - arteries and veins that collectively
connect to a main artery for blood supply. Medication for halting an organized
geometric structure called angiogenesis is provided to cancer patients to destroy
their tumors. So, we see that tumors without the position-differentiated cells
and organization to form geometric structures called angia or arteries cannot
survive.
Therefore, though it is explicitly said that cancer is a non controlled undifferentiated
multiplication of cells, the opposite is also clearly admitted - cancer cells
also differentiate in an organized form, for example in arteries.
We may call the factor here that differentiates and gives the particular form
to new born cells and geometry to the tumor that was non-existing before,
the etheric archetype of the tumor that gives organization to it, enabling
it to survive.
We shall also postulate here that this form factor is also the same as the universal
form-factor once called the “ether” by Aristoteles and that is present everywhere
in the Universe, as in the great variety of examples we have given above.
To understand the rest of this presentation, we shall also state here, as postulates,
two basic principles which govern this non material form of etheric archetype
that associates with the material structure of every object, based on many
years of relevant observations and experimentations in several different scientific
branches.
1. the Principle of extendibility of etheric archetype, i.e., its tendency to
copy or extend itself to any available material carrier.
2. the Principle of fractal information for the etheric archetype, i.e., to
store all the form information irrespectively in any point of the structure
of the associated object.
We are suggesting here, that the methods of treating cancer should be based
on controlling one or more of the factors, governing the above self-sustained
mechanism of lack of energy and shelf-organized division, which is creating
more need for energy, for the induced population growth. We call this suggestion
the “constructive” treatment of cancer, as opposed to the “destructive”
treatment described below.
For more see http://www.papimi.gr/cancer.htm.
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© 2000-2012 Weisser
