CELLULA CANCEROSA
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Sunday, 05 September 2010
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Evolution of the cancer process


What happens in tissues when the T infection is too strong and the defensive reaction of the organism is too weak?


The T infection stimulates the formation of strong blue vescicles (bions) that develop as defensive reaction from the cells of the interested tissue.


The blue vescicles (bions PA) are produced from the interested cells as contrast function and are a natural reaction of the organism defence against T infection.


If the reaction was limited to this and the vescicles did not have the natural predisposition to agglutinate, the cancer dont would exsist.

It happens instead that the energetically weaker is the organism and more abundant will be the production of blue vescicles in order to face the T aggression.


The great concentration of blue vescicles favours the natural capacity of aggregation in more advanced biological structures that become the well-known cancer cells.


At the beginning, the cancer cells are not born like carriers of disease but like by-products that develop from the organism defence against morbid processes.


The damaging of a tissue, the appearance of the corpuscles T from the bioenergetically weaker cells, the production of vescicles from the healthy tissues as defensive answer to the T invasion and the reorganization of the bionous masses in cancer cells with all its evolutive steps are only the first part of the cancer process.


Indeed a second even more important and opposite to the previous part exists.


It consists in the death of the cancer cells, arrived at the end of their vital cycle, and in the consequent decomposition in corpuscles T that produce a more intense putrefaction of the blood and of the tissues. And then the generalized and total poisoning of the organism.


What that provokes the death of the patient is not the formation of the living cancer cells but rather the secondary putrid T decomposition that develops from their death at the end of the vital cycle.


If at the beginning, during the formation of the first cancer cells, the damage is only locally limited, the successive death of the cancer cells that compose the tumour mass is instead the cause of a gigantic acceleration of the putrefaction of the whole body.


It is for this reason that we observe the cancer patient to resist for a long time to the disease and then to collapse, nearly suddenly, destroyed from one galloping cachexia that leads to the death in a very short time.


Contrarily to the first phase that can last years, the second phase lasts only few weeks.
The formation of the corpuscles T and the putrefaction of the cancer cells are therefore cause and effect of the cancer process.


This aspect has enormous importance for therapeutic ends.


When the tumour, the tissues and the blood are found in the putrid decomposition phase (Ca5), a large quantity of T bodies form in such a way to make the therapy useless.


It can be understood that all the therapies that try or that will try to kill only the cancer cells, not only they will not solve the problem but they will lead even to an acceleration of the above reported process.