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The Science of Homeopathy – page 147

quickly to the hypotoxic doses are given the same remedy in the thir- tieth potency, again with 25% receiving placebo in randomized fash- ion. This is repeated once daily for a period of two weeks. The sub- sequent observation period should be continued for at least another three months, or until it is obvious that no more new symptoms are emerging. As usual, if symptoms arise immediately, further doses are discontinued, and symptoms continue to be recorded under strict con- ditions until they are finished. When all symptoms have ceased, the prover may turn in the diary to the panel of experimenters and return home.

The final administration of a high potency should be delayed for a full year, during which time less formal observations can be made in the subject’s normal environment. After this period of rest, the same subjects who received the thirtieth potency gather again in the rural experimental environment and spend another preparation period re- establishing “baseline” observations. They are then given one dose of a 10M or 50M potency (again with 25% receiving placebos), and observed intensely for a further period of three months, or until symp- toms have ceased.

At the conclusion of the experiment, the panel of experimenters col- lects all notebooks and, one by one, lists every symptom which repre- sents a deviation from the subjects’ normal state. The experimenters should meet with each subject and try to elaborate and clarify each symptom as carefully as possible – describing thoroughly the exciting causes, the timing, and the modalities. Finally, the experiment is “un- blinded.” Symptoms generated by placebo subjects are deleted from the records of the test subjects, unless there is a marked discrepancy in frequency or intensity. The experimenters then collate all the remain- ing symptoms and present them for publication.

 

Formulation of Materia Medicas

 

In the birth and emergence of a remedy, the above-described ex- periments are the first step. Such strict experiments, plus whatever in- formation is available from toxicological literature, provide the raw data which form the basic foundations for the utilization of the remedy. As elaborate and detailed as the information is, however, it is as yet incomplete until tested clinically. The remedy is administered by reli- able prescribers to sick people according to the symptoms generated in the provings. As clinical experience grows, careful records are made of symptoms which are cured during the process of a real cure of the entire patient on all three levels. It is very important to understand that