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FOURTH LAW : THE ROLE OF MICROBES
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In
the meantime, the continuous progress of biochemistry brought more and
more complex information about the reactions of our cells and, more in
particular, about the leukocytes when facing those microbes: when they
pullulated with diseased, one assisted to an enormous confusion among
these leukocytes, as well as to the synthesis of numerous substances and
to microbial destruction phenomena. The result was the conception of an
immune system being our natural defence against invisible enemies,
all the more dangerous since they pass on from a diseased to a sound person,
implying a risk of contamination.
The last step "confirming" the infectious theory is the advent of drugs meant to support our immune system most often judged defective: the antibiotics and assimilated products. These drugs killed the microbes or prevented their multiplication in vitro, i.e. in laboratory cultures, and often relieved the symptoms in vivo, i.e. with the infected diseased. The development of the micro-organism’s catalogue, of molecular biology and of the mediatisation of the medical know-how did the rest: today, the civilised man’s culture is thoroughly impregnated with the microbes’ … for his highest fear. The vision of the infectious phenomenon may seem very logical, but numerous researchers have, however, found incoherences, gaps and disconcerting questions. Let us briefly summarise them. If a large number of microbes are responsible for our diseases, infinitely more are the harmless ones which are even indispensable to life such as the billions of germs inhabiting our body : there are thus good and bad microbes. In a large number of infectious diseases, our own usual microbes start to proliferate: good microbes can thus become bad ones. There are some becoming "resistant" to antibiotics. In a lot of bacteria and especially in viruses, a change of structure and properties occur: why those mutations, in which HIV is a mere champion? Contagion rather obeys to statistics than to constant rules and the presence within the body of germs considered dangerous does not necessarily lead to disease: why such a difference in "sensitivity" and "malignity" between individuals? At the start of the century, some daring persons ingested germ cultures from patients deceased from cholera without even getting the disease themselves. The general tendency on which converge these critical considerations joins the renowned (?) quotation of Claude Bernard: "Pasteur was wrong. A microbe is nothing. The site makes everything". And to extend on the balance of forces between the microbe and its host and all factors susceptible to disturb this balance. Confronted with these findings "in the field" science comes back in force describing always more thoroughly the shocks and misfortunes of an immune system supposed to have the monopoly over defence, and consequently over the famous balance. But all this only ends up in displacing the problems: why the weakness or the force of our immunity? It is this fourth biological law that is going to get us out of this theoretical labyrinth by continuously integrating the missing link called psychism – or, more exactly, the triad psychism-body -brain – and by funding only on verifiable observation facts. "The ontogenetic microbial system" shows us two realities: the microbes will only interfere in the second phase and spread according to the embryonic origin of the tissues (ontogenesis). The microbes only proliferate after the solution of the conflict obeying to the order of the brain that has, therefore, inverted its action mechanism now oriented towards reparation. They consequently participate in the recovery of the organs formerly affected during the conflictual phase. Their "job" consists in destroying, cleaning up or settling the lesions; this, of course, in an inflammatory climate, the discomfort of which will be proportional to the work to be done. When lacking these collaborators, recovery will only be slower and/or incomplete. If artificially neutralised by means of drugs, they will take up their activity later on ("relapse"), eventually by means of their mutation ("resistance"). Pure contagion is only a limited laboratory experience: an individual can only be contaminated while developing a lesion in the second phase of his disease and the extent of his infection will be determined by the extent of the harm done after his conflictual phase and not by the virulence of the germ in itself nor by the infection observed in the "contaminator". The micro-organism must suit the repairing tissue of the "contaminated" person. Most often our own microbes will start to proliferate at the site and, for a certain period; our cerebral computer will determine both. But numerous germs are latent in the endemic state, ready to "invade" us when needed. As far as the epidemic is concerned, it is another reality that can be understood in the light of the biological laws. Here, infection gains a large number of individuals and the microbe "seems" to spread out strongly, thus "seeming" to confirm the myth of contagion. But the same conflict may concern more than one person at the time. We will take three schematic examples as an illustration. A patient may develop hepatitis some time after his partner because he solved the same conflict, worrying the couple, at a later moment. An entire army may end the invasion of its country and, after this conflict is solved, the Spanish, Asian or whatever influenza may decimate a large part of it (but not all!). Cholera is effectively devastating populations knowing it means to lack the power of ingesting food and that are on the outlook for the tiniest hope for a humanitarian action… And let us not forget that famine caused by war or by overexploitation of certain countries is not at all favouring the tremendous reparations following the complete or temporary solutions of the conflicts. Each one of our tissues derives from one of the large embryonic layers and this origin is the criterion of choice of the different microbial types. Without going into details, let us precise here that the fungi and microbacteria destroy the proliferation occurring during the conflictual phase; it is for example the role of the tubercle bacillus which eliminates intestinal, lung or hepatic tumours. In function of the tissues, bacteria assume a similar destructive role in case of proliferation during the conflict or a clearing role previous to reconstruction in case of necrosis during the conflict. Finally, viruses contribute to filling up substance losses within ulcerated tissues during the conflictual phase. If infection participates to the difficult restoring phase, it may also need, as do all other symptoms of suffering, a therapeutic intervention, but essentially in two well-defined eventualities. First, when its extent (reminder: to be explained by the first phase) presents a vital risk for the patient, more in particular at the two extreme ages of life and with too weakened persons. One can then, concretely, be led to decelerate it more or less strongly, including by means of chemical drugs. Second, the "infestation" by microbes not foreseen in our ecosystem, as it is the case for tropical diseases; the plasmodium of malaria is not foreseen for western "visitors"; nor is the paramyxovirus of measles for the Indians of America (adult ones since measles are part of early childhood’s conflict). Transportation within a few hours to the other side of the planet certainly is an interesting feat, but the subsequent microbial import – export is not (yet) programmed by nature… With this fourth law, what remains of our immune system? Only the undeniable facts being the numerous biological modifications observed, but that have to be re-incorporated into a more global view: the immune system is a modulation mechanism of the microbial activity. During the conflictual phase, it is at rest, whatever the damage to and the weakening of our organs. As soon as the conflict is solved, it lets the microbes proliferate and act during the reparation phase and "dismisses" them when it is finished. Such a modulation mechanism is necessary as microbes are autonomous living organisms and thus proliferate naturally. The balance host–microbe is the conviviality between the large organisms and the micro-organisms, dating from the emergence of the living world and it can only be maintained as such according to the biological laws ruling the functioning of the living entities. This conviviality is but a special case of the existing balance as soon as a cell population is concerned: without even talking of microbes, the cells of our tissues are already submitted to ancestral reproduction rules. During our embryonic development, we pass from the microscopic size of one single cell to three or four kilos within nine months: why, when reaching the age of fifty, do we not reach the size of a house? Instead of such a lengthening, our growth curve bends until we leave puberty to finally only permit the replacement of dead cells by their own ageing cycle or by the destiny of their function. These regulation orders, though, (including those of puberty maturing) are sent out by the cells of the nervous system (that are, on the other hand, the only ones incapable of reproducing!). How can one then still ignore the role of the brain in this "revival" of multiplication that is the tumour phenomenon? It is by observing the constant relation between microbial functioning, organs, brain and psychism that Dr. Hamer was able to retrace the great biological laws showing the coherence between health, disease and the reversible passage from the one to the other. The table hereafter gives a synthetic overview of the four laws. On the next page, the reader will find a more complete table drawn from "THE FOUNDATION OF THE NEW MEDICINE" (page 246 of the French edition), which, however, particularly considers the cancerous phenomenon (it is but only in 1987 that he systematises the fourth law).
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