Why Sodium Chloride Molecules In Our Food Articles Do Not Antidote Potentized Natrum Mur?

As per the scientific understanding of homeopathy proposed by Dialectical Homeopathy, active principles of potentized drugs are ‘molecular imprints’ of constituent molecules contained in the drug substances used for potentization. Exactly, ‘molecular imprints’ are considered as supra-molecular clusters of water-alcohol molecules into which the three-dimensional molecular configuration of guest molecules(drug molecules) are imprinted as nanocavities. These ‘molecular imprints’ will have a specific affinity towards the original drug molecules, as well as other molecules having similar functional moieties, and can bind to them. Potentized homeopathic drugs act as therapeutic agents due to this configurational affinity towards pathogenic molecules having similar functional moieties.

According to this view, crude drug molecules will have an affinity towards their own molecular imprints due to their complementary configuration, and can specifically bind to them. As such, drug molecules should be capable of deactivating their potentized forms by binding to the molecular imprints. Due to this reason, it is commonly advised not to administer mother tinctures and lower potencies of drug substances when the patient is undergoing treatment with higher potencies of same drugs.

A question commonly raised in this connection is, why NATRUM MUR in high potencies are not antidoted by the use of molecular forms of sodium chloride as part of daily diet. If crude molecules of a drug substance could antidote its potentized forms, potentized Nat Mur should be deactivated by sodium chloride we consume. As per our experience, such an antidoting does not happen. If potentized Natrum Mur is used as similimum, it acts well even if the patient consumes sodium chloride as part of his food. Many articles used as spices and culinary during preparation of foods are also used as therapeutic agents in high potencies, and many of them do not deactivate potentized forms, where as some are found to be antidotal to potentized drugs. A logical and scientific answer is required for these reasonable questions.

When administered into the organism as medicinal agents, ‘molecular imprints’ contained in potentized drugs are released into the blood stream, which is a saline aqueous medium. Crude molecules of sodium chloride being consumed as food are also released into the blood stream.

The question to be answered is, how the molecular imprints of sodium chloride can exist in the blood stream without getting bound or antidoted by crude sodium cholide molecules present in blood, in spite of the configurational affinity between them.

To get an answer to this question, we should understand some important factors regarding the behavior of sodium chloride in aqueous medium.

Sodium chloride is an ionic substance, composed of positive charged sodium ions and negative charged chloride ions. In solid state, each ion is surrounded by six ions of the opposite charge as expected on electrostatic grounds. The surrounding ions are located at the vertices of a regular octahedron. In the language of close-packing, the larger chloride ions are arranged in a cubic array whereas the smaller sodium ions fill all the cubic gaps or octahedral voids between them. The attraction between the Na+ and Cl- ions in the solid is so strong that only highly polar solvents like water can dissolve NaCl well.

When dissolved in water, the sodium chloride framework present in solid state disintegrates as the Na+ and Cl- ions, and become surrounded by the polar water molecules. These solutions consist of positively charged metal-aqua complex with the formula [Na(H2O)8], consisting of a sodium ion closely surrounded by eight water molecules. This sodium-water complex by itself acts as positively charged ion. The chloride ions are also strongly solvated, each being surrounded by an average of 6 molecules of water.

Important point to be noted here is that Na+ ions or Cl- ions never exist free in the aqueous medium, but only as surrounded and strongly solvated by water molecules. Since the sodium and chloride moieties are covered with closely packed water molecules, they cannot interact with the molecular imprints contained in potentized Natrum Mur present in the medium. Na and Cl ions have a comparatively greater affinity towards the water molecules around them, than towards molecular imprints. Due to this reason, potentized Nat Mur cannot be easily antidoted by crude sodium chloride molecules consumed as part of regular diet. This is applicable to all drug substances that are ionized and strongly solvated in aqueous medium.

Author: Chandran Nambiar K C

I started practicing homeopathy in 1970, when I was 20 years old and studying for final year of BSc (Zoology) course. My interest in homeopathy happened very accidentally, through a constant relationship with a local practitioner who happened to be father of my classmate. I was a regular visitor in his clinic, where from I started reading BOERICKE MATERIA MEDICA and other homeopathic books, which helped me to cure myself my troublesome asthma that have been haunting me since my childhood days. I became a voracious reader of homeopathy. I was also deeply involved in studying marxism and dialectical materialism during my college days, which attracted me to political activities. MARXISM and HOMEOPATHY became two essential parts of my intellectual and practical life, which still continues so. Even though I joined DHMS course in a karnataka homeopathic college, I could not continue it due to my intense involvement in revolutionary political activities that resulted in jail life and a lot of criminal cases. Once that phase was over, I took a diploma in veterinary science and became a livestock inspector in animal husbandry department under govt of kerala. I have been continuing my study and practice of homeopathy all through these years. Since CCH act came into force only in 1976, and it contained provisions allowing existing practitioners to continue, my homeopathic practice went smoothly in parallel with my government job. In 1987, co-operating with some local homeopaths and social activists, I started Kannur District Homeopathic Hospital Sociey, which established a chain of hospitals and homeopathic clinics in different parts of Kannur district. After a few years I had to leave the society for some political reasons, and I established a 100 bedded well equipped homeopathic hospital in Taliparamba, employing a number of prominent homeopaths. That was ended up as a financial disaster for me due to many reasons, including my lack of skills as a money manager, and I was compelled to close down my dream project with in a short period. I lost huge money I invested, lost my reputation, and it pulled me into a debt trap. I learned a lot of valuabl lessons from this failure- about life, human psychology, relationships, and above all, about myself. I realized failure is the greatest teacher, if you are prepared learn from it. I learned how will power and determination to win will help us come back into life as a phoenix from our own ashes. I learned, one does not fail unless he stops fighting and accepts failure. My failure and the hardships that followed has moulded my personality in such a way that I can now withstand any disaster and fight back. I tell you, you will not know what life really is, unless you miserably fail at least once in your life. By this time, I left my government job also, and settled as a full time homeopathic practitioner. By this practice, I could repair my earlier financial losses, and establish well in life. It was during this period that I felt the need of developing a simple and user-friendly homeopathic software, that resulted in the evolution of SIMILIMUM, which was later upgraded into SIMILIMUM ULTRA. Similimum Ultra was well accepted by the profession, and it collected good revenues which continues even today. I stopped my practice a few years back , and concentrated in the study and research activities to evolve scientifically viable explanations to the so-called riddles of homeopathy. This unrelenting study resulted in MIT or Molecular Imprints Therapeutics, which provides a scientific and rational explanation for homeopathy. I started a homeopathic discussion group on facebook called HOMEOPATHY FOR TOTAL CURE, which has more than 35000 homeopaths as members. By this work on facebook, I could establish close relationship with many homeopaths around the world. It goes on. I could successfully convert facebook as my office and work place, from where I propagate my MIT ideas, co-ordinate my works for homeopathic community, and sell my Similimum Ultra Software. My years of hardwork in search of HOW HOMEOPATHY WORKS ultimately resulted in the publication of a book titled REDEFINING HOMEOPATHY (3000 pages, 3 volumes, hard bound, Rs 6000), in which I have compiled my articles regarding my scientific explanations of basic principles of homeopathy. These ideas are called MIT or MOLECULAR IMPRINTS THERAPEUTICS. MIT is now included in the syllabus of MD (HOM) course of prestigious DY PATIL DEEMED UNIVERSITY, PUNE, INDIA. Research department of SARADA KRISHNA HOMEOPATHIC COLLEGE, Kulashekharam, Tamilnadu, India, the only NAC accredited homeopathy college in India, has recently taken up certain reserch projects for proving the scientific explanations proposed by MIT. Based on MIT perspective of homeopathy, I had developed an MIT PROTOCOL for scientific homeopathy, and initiated a project for establishing a chain of MIT NETWORK CLINICS all over India, where MIT PROTOCOL will be practiced. More over, I have developed a whole range of 351 MIT FORMULATIONS, which are disease-specific combinations of post-avogadro diluted homeopathy drugs. NOW I AM IN 71st YEAR OF MY LIFE, AND STILL LOOKING FOR NEW HORRIZONS!

3 thoughts on “Why Sodium Chloride Molecules In Our Food Articles Do Not Antidote Potentized Natrum Mur?”

  1. Sir, when you say “pathogenic molecule is also a molecular imprint of a disease”, it means you are not using the term ‘molecular imprint’ in its specific scientific meaning. “Molecular imprint’ is only a recognition site imprinted in the medium as three dimensional nanocavities, in a configuration just opposite to that of original molecule. “”pathogenic molecule” cannot be a “Molecular imprint”.

    “NaCl can not counter NaCl in its potentised form(Nat mur) as their chemical structures are basically the same and they act in unison” is also not correct. “Molecular imprints’ have no ‘chemical structure’. Molecules and their molecular imprints can bind each other, and antidote each other, since their configurations are complementary, molecules acting as ‘keys’ and ‘molecular imprints acting as ‘locks’.

  2. Correct me if I am wrong, Mr. Nambiar, but my take on potentised remedies vis-a-vis its crude form is as follows.
    1. A bio pathogenic molecule is also a molecular imprint of a disease and to inactivate it one needs to counter it with a remedy in its ‘molecular imprint form’ so a fast bonding and inactivation can take place.
    MTs and crude remedy forms should be used to correct structural deformities(bone, etc.) that are basically produced by ones internal system or to repair damages eg. Calc carb for bone knitting, etc.
    2. A crude form of a remedy can not counter its potentised form. In other words NaCl can not counter NaCl in its potentised form(Nat mur) as their chemical structures are basically the same and they act in unison – otherwise the first dose of Nat mur would be antidoted by a second dose of Nat mur and therefore, a remedy could never be repeated; whereas, in fact and in an acute ailment a remedy is repeated even every 5 minutes for speedy control.

  3. Not only the molecules of sodium even the potassium or calcium or even the minerals such as phosphorus, sulfuric .Zink, copper never inter-fear with the homoeo drugs action. .Rather their physiological presence and chemical structure with combination of various proteins and enzymes related to that particular molecules or mineral with dense aqueous medium and cellulose exist in the body their by provides needed kinetic energy, nutrition and resistance or immunity that maintains the health of the human body. What is their to get doubt and the question of anti doting never arises. A medical person who is accustomed with cell structure never gets such doubts rather he understands the cell mechanism. This particular cell structure made the homeopathic drugs to produce few symptoms when they proved on humans and this particular cell structure prevented various symptoms which were not produced but mentioned in materia medica. Because of presence of cell mechanism which I need not write here as already mentioned in the texts of molecular biology almost all homoeopathic drugs produced only few symptoms when they were proved on humans. The maximum symptoms produced are 7 seven symptoms only by sulphur and Lycopodium (provers symptoms). Rest of the symptoms written in materia medic are verified symptoms which were deemed as unscientific in the present day context. There fore this lack of understanding the basic cell structure and molicular biology making homoeopaths not to understand thair merits as well as thair demerits. But most of the allopathic drugs interfere with cell machanisum and the action of the various drugs will be from sodium, potassium calcium and glucose chains which you know very well.

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