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www.papimi.gr/cancer.htm

Professor Pappas' Theory of Cancer

Developed by Professor P.T. Pappas
based on the experience of PAP IMI results, over the last ten years.

Original January 21, 1998
Upgraded version 25/1/ 2004, minor corrected February 3, 2004
© 1998-2002 by P.T.Pappas. All rights reserved.

The present article consists of a publication of an original theory and idea by the author, presented here for the first time world wide.
No part of this text may be reproduced in any form without the expressed written consent of the author. No idea presented here for the first time may be expressed or transmitted in any form without ethical acknowledgement and proper due reference to the author. 

THE PRINCIPLE FOR THE CURE OF CANCER WAS KNOWN SINCE SOME SEVERAL THOUSANDS YEARS
Cancer is a low metabolism state of starvation for a group of cells. www.papimi.gr

We would like to state a more consistent theory of cancer that we came up with, based on ten years of experience. The results are fascinating, obtained after PAP IMI exposures, and after comparing these results with other theories and methods.

The first assumption involves the most basic principle of physics, which we have come to realize several years ago in association with cancer. The assumption concerns the physical energy of the cell. Energy in physics, as in the universe as a whole, is the most fundamental and universal concept of cause and effect. This controls every action in the cosmos, between a donor of the energy [the cause] and a receptor of the energy [the result]. We may say, a biological system with energy transformed from one form to another or given from a donor to a receptor, is a living system. A biological system with active metabolism and energy not given and taken between donors and receptors (without metabolism) is a dead system. We state below an extremely simple and fundamental principle for cancer in relation to the physical energy condition of a cell.

We would like to state a more consistent theory of cancer that we came up to, based in ten years of experience with the fascinating results obtained after PAP IMI exposures, and, compare these results, with other theories and methods. The first assumption concerns the most basic principle of physics, which we have come to several years ago in association with cancer. The assumption concerns the physical energy of the cell. Energy in physics, even in universe as a whole, is the most fundamental and universal concept of cause and effect, which controls every action in the cosmos, between a donor of the energy - the cause, and a receptor of the energy - the result. We may say, a system with energy transformed from one form to another or given from a donor to a receptor, is an alive system. A system with energy but not given and taken between donors and receptors is a died system. We state below this extremely simple and fundamental principle for cancer in relation to the physical energy condition of a cell.

Cancer is a critically low state of energy within a cell and with a critically low metabolism, in which the cell is being "trapped" for various reasons. This critically low energy and metabolism state is manifested by a low transmembrane potential (TMP) of 15mV, which causes a "chain" of specific malfunctions for the cell, and a general state of ischemia (low energy) for the organism . When a cell is in this particular low energy/metabolism state and has below TMP of 15mV that is responsible for cell metabolism (Nobel Laureate Albert Szent-Györgyi, Cone and others). The extremely weak TMP of 15mV cell divides in two identical parts in an attempt to survive in larger numbers as a species.

Cancer is also the most general phenomenon of missing cell energy , low metabolism and division in biological systems. It is a phenomenon found in all forms of life, i.e., plants, animals and, we may even say, in all living societies such as that of humans, animals, plants, and various micro-organisms.

We may suggest that Cell Cloning, Meristomatic Culturing for plants and Cancer, all have the same starting point in common for cell proliferation, that is metabolic stress, or poor nutrition, long known for cell cloning and meristomatic culturing for plants.


We demonstrate the above, with a common example taken from agriculture, which is known to most farmers: Let us suppose that we have two plants which we water every day. The plants stay healthy, but as a result do not produce flowers or seeds, which would lead to reproduction of the plant. If we deprive one of the plants of its nutrition by halting the water supply, as a result you will find the plant in a state of "stress". This plant will then produce flowers and seeds in order to multiply and thus survive as a species. This result is due to an "instinct" or "survival program" deeply encoded in its DNA by its creator. This is a general phenomenon of reproduction, known for almost all plants.

The same holds true for advanced organisms which may secure food fairly easier versus a primitive one, which strives every day for food. Indeed a primitive organism is in a continuous state of stress while finding food and energy. In order to counter this and overtake its daily battle for food and survival as a species, it multiplies very fast and in large numbers.

On the contrary, an advanced organism or animal multiplies relatively very slowly, and in fewer numbers. For example, larger animals such as elephants or humans multiply very slowly, in comparison to a smaller animal such as a rabbit or a primitive organism.

The same is true for a poor, versus a rich society. For example, in poor couples of primitive societies we will find that they usually have between five and eight children. In comparison, the couples in rich societies tend to have one or two children.

Cancer environment, diffusion and metastasis: When a low energy proliferating cell is found to be lacking the proper nutrition and energy, many times this is so because it is surrounded by an adverse environment. This environment can be an anaerobic (non-oxygenated) one, which is limiting the "energy providing synthesis" of Na and O to K. Shortage of nutrition and energy may also be due to the fact that cells are adjacent or are surrounded by another tumor, or other low energy cells with limited veins and arteries. When a tumor is starving for energy and nutrition, the starvation is transmitted to the neighbors. Obviously, adjacent cells will suffer for proper oxygenation, nutrition and metabolism. Removing energy and nutrition by a tumor from adjacent cells, may cause a similar shortage of energy and nutrition, thus cancer diffusion and cancer metastasis to adjacent cells.

We can say, proliferating cells in an energy crisis, cause a similar "energy crisis" to nearby cells. In other words, the energy crisis of a smaller area of cells, is diffused or extended to a broader area, because of the most basic and fundamental principle of physics, the principle of the conservation of energy and the principle of conservation of matter.

This crisis of low energy is reflected in the following general chain reactions and results:
+ low transmembrane potential
+ increased accumulation of sodium ions inside the cell: Hypernatremia
+ increased water molecules attached to sodium molecules inside the cell associated to hypernatremia
+ inflammation
+ increased volume of the cell and osmotic pressure inside the cell, damaging the cell membrane
+ swelling
+ thinning of the cell membrane
+ 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., Tokio, Japan, ISBN4-939098-00-1, 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 www.papimi.gr/cancer.htm.

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