How To Explain The Phenomenon Of ‘Homeopathic Aggravation’ Scientifically??
Now, let us take up the issue of so-called ‘homeopathic aggravations’. This phenomenon is very much discussed by homeopaths. It is true that in many instances we experience such aggravation of symptoms after prescribing homeopathic medicines. Some homeopaths believe that aggravations occur due to wrong prescriptions, whereas consider it happening as part of curative process due to ‘exact’ prescriptions. Some homeopaths differentiate between ‘medicinal’ aggravations which are harmful, and ‘homeopathic’ aggravations which are welcome.
In my opinion such ‘aggravations’ are not due to ‘prescribing wrong drugs’ or ‘exact drugs’, but due to prescribing drugs that cover only part of the ‘symptom complexes’ present in the patient. To follow what I say, one should be well aware of the concepts of ‘molecular errors’ underlying pathology, as well as ‘molecular imprints’ present in potentized medicines. As per our view, an individual will be having multitudes of ‘molecular errors’ caused by binding of diverse types of pathogenic molecules on different biological molecules. Each individual ‘molecular error’ may be expressed in the form of specific subjective and objective ‘symptom complexes’. If we select a drug as a similimum on the basis of some of the leading symptoms only, ignoring other symptoms, that similimum in fact covers only some of the molecular errors. The ‘molecular imprints’ contained in that similimum may remove those molecular errors only. But other molecular errors remain. The ‘symptom complexes’ representing those remaining molecular errors would become more expressive and come to the fore. In the absence of scientific understanding regarding the molecular processes behind this phenomenon, we happen to interpret these new expressions as ‘homeopathic aggravation’.
We experience many instances of wonderful cures that do not obey “Dr.Kent’s 3rd observation” or “Hering’s Law”. They are not universal laws of homeopathic cures. They are all only speculative theories based on isolated experiences. Many of such ‘principles’ and ‘laws’ will have to be abandoned as our scientific understanding of real process of homeopathic cure become more and more perfect and accurate.
Most of us would have experienced some initial aggravations followed by complete relief. We should understand ‘molecular errors’ not as singular static incidents. A particular molecular error caused by a particular pathogenic molecule may result in cascading of new molecular errors. It is like a traffic block in a city. A small traffic block may cause cascading of traffic blocks, ultimately resulting in total failure of traffic system in the city. When a molecular error occurs in a particular biochemical pathway in the organism, it may affect other related pathways also. That is why diseases progress expressing trains of new symptoms. When we start removing these molecular blocks, there may be readjustments happening in all these related biochemical pathways, which may appear as aggravations of symptoms. That is part of normal curative process.
That means, when studying the phenomena of ‘homeopathic aggravations”, both chances will have to be considered. “Re-adjustments’ happening in various biochemical pathways as part of curative process, as well as ‘appearing of remaining symptoms’ because of prescription being partial.
When we follow the TOTAL CURE METHOD proposed by MIT, we prescribe a combination of drugs that would contain all the ‘molecular imprints’ required to rectify all the ‘molecular errors’ covering all ‘symptom complexes’ expressed by the individual. Hence, so-called ‘homeopathic aggravations’ are never experienced in TOTAL CURE PRESCRIPTIONS.
Homeopathic CASE FOLLOW UP consists of watching for RESIDUAL SYMPTOMS and EMERGING SYMPTOMS, and re-adjusting prescriptions as indicated by them.
After making a homeopathic prescription, whether it be ‘single’ or ‘multiple’, and ensuring that the doses are used in right potencies and repeated in optimum frequencies, the physician should see the patient at reasonable intervals and carefully watch how the case is progressing.
Periodically watch for ‘residual’ symptoms that do not subside, as well as newly ’emerging’ symptoms.
If a particular ‘group of symptoms’ remain in spite of frequent repetitions of doses for a reasonable period, that means our prescription failed to provide the particular ‘molecular imprints’ required to remove the molecular inhibitions underlying that particular ‘group of symptoms’. Repertorise using those ‘residual’ symptoms, find a similimum for them, and add it to the original prescription.
If new symptoms ’emerge’, and they are not subsiding within a reasonable period, that means some ‘hidden’ molecular inhibitions not covered by the original prescription has come to the forefront during the removal of some other molecular errors. Find a new similimum for these newly emerged symptoms and add it to the original prescription.
We will have to continue this constant watch for ‘residual’ symptoms and ’emerging’ symptoms and adjust prescriptions all through the whole course of treatment, in order to ensure a TOTAL CURE.