I do not think modern medicine is irrelevant. It plays main role in the health care system all over the world. ALLOPATHY Hahnemann talks about is no more. It is not fair to call ‘modern medicine’ as allopathy. Modern medicine is ‘molecular medicine’, based on scientific understanding of vital processes. Remember this point when quoting ‘ant-allopathy’ statements of our masters. Fundamental difference between homeopathy and modern medicine is that ‘modern medicine’ uses ‘drug molecules’ as therapeutic agents, where as homeopathy uses ‘molecular imprints’ of drug molecules. This is a very important difference, indeed.
MODERN MEDICINE has recently advanced into MOLECULAR MEDICINE, where drugs are selected on the basis of scientific understanding of pathological molecular errors in vital processes. Homeopathy selects drugs on the basis of ‘totality of symptoms’, which are the real indicators of those pathological molecular errors. As such, homeopathy can be defined as a specialized higher branch of ‘modern molecular medicine’.
Since ‘modern medicine’ uses highly reactive ‘drug molecules’ as therapeutic agents, they can create dangerous ‘off-target’ molecular errors in the organism. That is the main draw back of ‘modern medicine’. Since homeopathy uses only ‘molecular imprints’, they cannot cause any ‘off-target’ molecular errors. Hence homeopathy is very safe when compared to modern medicine.
Since ‘modern medicine’ requires a clear understanding of pathological molecular processes to decide an appropriate therapeutic agent, they cannot treat many diseases which are not well understood. For homeopathy, knowing the exact molecular error behind the pathology is not necessary, since homeopathy identifies the molecular errors and their remedial agents by observing subjective and objective ‘symptoms’ that express the molecular errors. As such, homeopathy can cure any disease even without knowing the underlying molecular errors, merely on the basis of ‘symptoms’. This is a great advantage for homeopathy. Whereas modern medicine can hope for an effective treatment only for well understood diseases, that to with possibility of unwanted side effects, homeopathy can treat any disease effectively and safely.
Let those qualified in modern medicine do it. Homeopaths are legally, ethically and philosophically not permitted to practice modern medicine. As a medical system Homeopathy is qualitatively much above and different from modern medicine, if homeopaths approaches it scientifically.
In a far distant historical perspective, I foresee the possibility of converging of modern medicine and homeopathy into a universal molecular medical science of ‘drug-less therapy’, where only molecular imprints will be used as therapeutic agents.
Modern Medicine is gradually evolving into ‘Molecular Medicine’. Molecular Medicine studies vital processes and diseases at molecular level, and deals therapeutics as an art and science of molecular level repairing.
Molecular medicine is the most advanced, most scientific and most recently originated discipline in modern medical science. It is a broad field, where physical, chemical, biological and medical techniques are used to describe molecular structures and mechanisms, identify fundamental molecular and genetic errors of pathology, and to develop molecular interventions to correct those errors.
‘Molecular Medicine’ emphasizes disease and cure in terms of cellular and molecular phenomena and interventions rather than the conceptual and observational focus on patients and their organs common to conventional medicine.
Molecular Medicine studies drug substances in terms of their molecular level structure and organization, and is more and more relying upon target-specific Designer Drugs synthesized by drug designing technology, supported by computer aided designing protocols.
Drug Designing Technology has recently started exploring the possibilities of Molecular Imprinting in the development of target-specific designer drugs. They are now experimenting for developing bio-friendly imprinting matrices and imprinting protocols, so as to prepare artificial binding surfaces for pathogenic molecules that could be utilized as therapeutic agents.
Even though not yet recognized as such, homeopathic potentization is a process of molecular imprinting, where artificial binding sites for pathogenic molecules are produced by imprinting drug molecules into water-ethyl alcohol supra-molecular matrices. Homeopathy identifies pathological molecular errors and selects the appropriate molecular imprints through a peculiar technique of ‘comparing symptoms’, which is expressed as the therapeutic principle, ‘simila similibus curentur’
Most probably, modern molecular medicine and drug designing technology is in the new future going to explore the possibilities of water as a molecular imprinting medium as part of their search for novel substances to be utilized as imprinting matrix.
It means, Modern Molecular Medicine is slowly advancing towards the realization of a drug designing technology that homeopathy invented as ‘potentization’ and utilized for preparing therapeutic agents 250 years ago. It is based on this understanding that I try to propagate the concept that ‘Homeopathy is Molecular Imprinting Therapeutics- An Advanced Branch of Molecular Medicine.
In a far distant historical perspective, I foresee the possibility of converging of modern medicine and homeopathy into a universal molecular medical science of ‘drug-less therapy’, where only molecular imprints will be used as therapeutic agents. Instead of our present ‘potentization’, modern science may develop more sophisticated ways of molecular imprinting, that would enable us to produce therapeutic agents more specific and perfect than our present day ‘potentized drugs’.
May be be distant dream. But it is a dream based on scientific knowledge.
Even though modern medicine is more and more turning to target-specific designer drugs, ‘drug designing’ using water molecules and molecular imprinting in water are subjects still unknown to modern drug designers. Homeopathy has been using this technique for last 200+ years in the form of potentization. Once the ongoing search for new drug designing techniques and new substances for molecular imprinting finally land them inevitably into the understanding of ‘molecular imprinting in water’, modern medicine and scientific community will have to recognize homeopathy and its potentization. At that moment, they will have to recognize the genius of samuel hahnemann. It is only a matter of time to happen that. Wait and see.
Modern scientists would any time arrive at ‘drug designing by molecular imprinting in water’, and utilize it with out any mention of homeopathy or potentization. Actually, I am making all my ideas about MIT public with the hope that it may some how prevent modern medicine from turning “this discovery in ther side by some way” without recognizing homeopathy.
If a drug substance in molecular form is introduced to a healthy living organism, which exists in state of comparatively dynamic equilibrium, constituent molecules of that drug substance are conveyed by the internal transport systems, and bind by their configurational affinity to any of the complex bio-molecules engaged in natural biochemical processes. As a result of such molecular binding, the bio-molecules are subjected to deviations in their three-dimensional configurations, and becomes incapacitated to deliver their natural molecular functions. All the biochemical processes mediated or participated by those bio-molecules are affected, and dependent biological pathways are subsequently blocked. Since different biological pathways are inter-depedent, deviations in one pathway naturally affects the dependent ones also. The cascading of molecular deviations influence the neuro mediator-neuro transmitter systems and endocrine systems and finally manifest in the form of particular groups of subjective and objective symptoms. This is the real molecular kinetics of pathology.
Homeopathy has its own peculiar way of experimenting and documenting the properties of medicinal substances in relation with their capability to produce various pathological conditions. This is called drug proving. For proving a particular drug substance, it is introduced into a healthy organism, and, the subjective and objective symptoms and their modalities representing the diverse molecular deviations caused by the drug, are carefully observed and recorded. Each specific group of symptoms that appear as part of diverse pathological conditions are thus artificially created in healthy individuals. These symptoms are compiled as a materia medica of the substance used.
Even though modern biochemistry and molecular medicine has made great strides in the study of diverse molecular inhibitions related with diseases, still there are grave limitations. It is imperative that modern science should strive to find out means to define the exact bio-molecular deviations and inhibitions responsible for each and every one of the multitude of diverse symptoms and modalities expressed in particular disease conditions, in order to evolve a most scientific method of removing such inhibitions. Homeopathy considers “totality of symptoms” as the only clue to the understanding of molecular level pathology, as well as deciding the appropriate therapeutic tools to rectify that molecular errors. Viewing from this perspective, “similia similibus curentur” is a highly scientific principle of therapeutics, deserving to be greatly honored by modern science at least in coming days.
Potentized homeopathic drugs contain ‘molecular imprints’ or ‘hydrosomes’, which can bind to the exogenous and endogenous pathogenic molecules having complementary affinity, thereby relieving the protein molecules from molecular inhibitions. This is the molecular mechanism of homeopathic therapeutics. ‘Hydrosomes’ or ‘Molecular Imprints’ are nanocavities formed in the ‘supra-molecular clusters of water and ethyl alcohol’, by a process of ‘molecular imprinting’ involved in potentization. When introduced into the organism, they act as artificial binding sites for pathogenic molecules having complementary configurational affinity, thereby relieving the biological molecules from pathological molecular inhibitions. This is the most rational and logical explanation of molecular dynamics of homeopathic therapeutics.
’Molecular imprints’ can be compared to ‘antibodies’. Antibodies are native proteins subjected to ‘molecular imprinting’ by ‘antigens’, and acting as binding sites for the specific antigens. ‘Molecular imprints’ in potentized drugs are supra-molecular clusters of water/alcohol, subjected to ‘molecular imprinting’ by constituent molecules of drug substances, and acting as artificial binding sites for pathogenic molecules having configurational similarity to drug molecules used for imprinting.
It is obvious that potentized drugs cannot rectify molecular errors arising from genetic errors and nutritional deficiencies. Scope of homeopathy is limited to the diseases originating from molecular inhibitions of proteins by exogenous or endogenous molecules. Homeopaths should remember these fundamental factors while discussing scope and limitations of homeopathy.
In scientific terms ‘similia similibus curentur’ means, “pathological molecular inhibitions underlying a disease and expressed through specific groups of subjective and objective symptoms can be removed by applying ‘molecular imprints’ of drug molecules, which in crude form could produce similar molecular inhibitions expressed through similar groups of symptoms “.
So far, we understood ‘Similia Similibus Curentur’ as ‘similarity of symptoms produced by drugs as well as diseases’. According to modern scientific understanding, we can explain it as ‘similarity of molecular errors produced by drug molecules and pathogenic molecules’ in the organism. That means, ‘similarity of molecular configurations of pathogenic molecules and drug molecules’. To be more exact, it should be understood as ‘similarity of functional groups of pathogenic molecules as well as drug moecules. Potentized drugs contains ‘molecular imprints’ of constituent molecules or functional groups of drugs used for potentization. ‘Molecular imprints’ are three-dimensional negatives of molecules, and hence they would have a peculiar affinity towards those molecules, due to their complementary configuration. ‘Molecular imprints’ would show this complementary affinity not only towards the molecules used for imprinting, but also towards all molecules that have configurations similar to those molecules. Homeopathy utilizes this phenomenon, and uses molecular imprints of drug molecules to bind and entrap pathogenic molecules having configurations similar to them. Similarity of configurations of drug molecules and pathogenic molecules are identified by evaluating the ‘similarity of symptoms’ they produce in organism during drug proving and disease. This realization is the the basis of scientific understanding of homeopathy I propose.
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I agree all these contents, homeopaths should struggle to prove homoeopathy scientifically.