Transmission of Molecular Information on Molecular Structures and Amounts ofthe Molecules Through the Recorded Traces of Photons,Sound Waves,and Electric Currents Coming Through Biological Tissue and Their Clinical Application For New Non-invasive Diagnosis and Treatment of Intractable Medical Problems

Abstract

In 1984, the author discovered that photons passing through or going through the close vicinity of a certain molecule, can transmit information bi-directionally (in the direction of photon are traveling and the direction the photons are coming from) concerning the molecular structure of the molecule, the amount of the molecule present and its electromagnetic parameters. Subsequently the author succeeded in the extraction of visible or invisible molecular information from photographs, the film of X-rays, CT scans, MRI’s, and ultrasonic imaging, by the application of resonance phenomena between 2 identical substances.

In the early 1990’s, the author was asked indirectly by the Director of the Tokyo Zoo through Prof. T. Matsubara of Azabu University Veterinary Medical School in a suburb of Tokyo whether one can diagnose lions in cages without the examiner entering inside the cage and without making the lion unconscious by injecting an anesthetic agent. Using animals in Prof. Matsubara's institute, with his assistance, the author tested the feasibility of examining at a distance with the use of a pocket laser beam pointer and control substances, parasites in animals in penned areas or in animals moving freely, such as horses. Since this proved to be feasible, the author began to use this method for the screening of bacteria, viruses and parasites in both animals and humans without directly contacting them.

A few years later, this method was applied to the mass screening of cancer successfully by the author in Warsaw, Poland. A third person who serves as an intermediary without directly touching the patient, holds a miniature laser to radiate a red spectrum soft laser beam of less than 1mW while holding Integrin α₅β₁ as a reference control substance in the same hand. From a distance and without directly contacting the patient, the third person assisting in the indirect Bi-Digital O-Ring Test projects the laser beam at a distance of usually within 20m at the patient, who is to be examined, in order to detect any resonance between the control substance and the identical substance in the patient’s body. For quick screening of cancer (in about 2 minutes), the author radiates the laser beam at the hands and the legs of the patient, one by one, where the skin of the extremities is exposed. When there is a strong resonance between 60ng Integrin α₅β₁ and the same molecule inside the patient’s body, one can estimate the presence and approximate location of either cancer or pre-cancer often before it can be detected by standard laboratory tests such as X-ray, CT Scan, MRI or blood chemistry. Since the summer of 1999, in order to localize the exact location of the pathological areas of the entire body, we have been successfully using X-axis and Y-axis scanning with a bar of laser light instead of laser beam pointer. Using this technique, we often discover additional metastasis of cancer which was not even suspected with standard laboratory tests.

Since photons transmit molecular information, in the late 1980’s the author did an experiment by taking photographs of different molecules and then testing whether it was possible to identify each molecule from the photograph using the Bi-Digital O-Ring Test resonance phenomenon with a control substance. He found that it was possible to identify the substances and to determine the approximate amount semi-quantitatively. The author then tested whether disease information could be detected from a photograph of the skin above a diseased organ. It was also found that it is possible to determine a significant amount of information, although it is less reliable than using an X-ray, CT scan or MRI. In the early 1990’s, the author thought that X-rays (photons with very short wavelengths and can penetrate through body tissues) may also carry all the molecular information of the part of the human body that they pass through. This idea was found to be correct by repeatedly testing with a known control substance to detect resonance between the identical molecule inside the body. The author compared this findings from direct examination of the patient using the Bi-Digital O-Ring Test with the findings from the Bi-Digital O-Ring Test examination of the patient’s X-rays, CT Scans, and MRI’s. Using the Bi-Digital O-Ring Test, he found that even when an abnormality is invisible in the X-ray, CT Scan and MRI, the information obtained with the Bi-Digital O-Ring Test from the patient and from modem medical imaging devices is almost identical. Therefore, in cases where a patient cannot travel because of far distances or because of serious diseases, it is possible to estimate the cause of disease and potential treatment through the Bi-Digital O-Ring testing of the developed or printed X-ray, CT Scan or MRI of the patient’s diseased area. Some of these clinical applications were published in the mid 1990’s.

If the photons can transmit molecular information, the question was whether sound, such as ultrasonic waves, could also transmit molecular information when they pass through body tissue. Using ultrasonic imaging of normal and abnormal tissue, the author found the imaged organ will produce resonance with a microscopic slide of identical tissue. When the sonogram of a malignant tumor is tested, a substance which appears markedly in cancer, such as Integrin α₅β₁ or Oncogene C-fos Ab2 produces strong resonance. With the sonogram of a cancer of the uterus, when the monoclonal antibody of the Human Papilloma Virus is used as a reference control substance, a strong resonance is often produced.

Since the early 1990’s, the author also postulated that if the photons can transmit molecular information, biological electric cunent may also cany information about the location on the body tissue where the specific bioelectricity was generated or passed through. If this is true, the ECG should contain the molecular information about the areas of heart where each part of the ECG is generated or passed through body tissue. For example, with the author’s own ECG recordings, on the recorded ECG traces for the Standard Limb Lead ECGs and Pre- MolCordial ECG recordings, the right atrium tissue produces resonance at approximately the first 100 millisecond duration before the beginning of the P-wave, where the trace shows no visible potential. (This finding is somewhat contradictory to the present concept of the mechanism of the P-wave generation, but there must be some reason for it.) The SA node produces resonance during the early part of this pre P-wave period. The left atrium produces strong resonance during the entire visible P-wave up to the end of the P-wave, while other cardiac tissue will not produce significant resonance on the recorded P-wave trace. Between the end of the P-wave and the beginning of the Q-wave, Purkinje fibers produce strong resonance. On the QRS-wave complex, left ventricular tissue produces strong resonance at the QR segment, and the right ventricular tissue produces strong resonance at the RS segment. When the T-wave is examined, the left ventricle also produces strong resonance at the recording between the end of the S-wave and the end of the T-wave. But right ventricular tissue produces strong resonance at about a 100 millisecond duration after the end of the Twave. (This new information may explain the genesis of the U-wave, which often appears after the end of the T-wave, but the mechanism of the genesis of the U-wave is not well understood.) When the normal ECG is tested with the Bi-Digital O-Ring Test, the O-Ring will not open, but when there is an abnormality in the ECG and the ECG trace is tested with the Bi-Digital O-Ring Test without holding any substance, the O-Ring will open. When the ECG trace is tested with effective medication, the O-Ring will no longer open. In addition, when cardiac tissue is infected by bacteria or a virus, a microscope slide of the bacteria or the monoclonal antibody of the virus produce significant resonance, depending on the degree of infection. Also, drugs taken by the patient that exists in the heart can be detected from the recorded ECG trace by the Bi-Digital O-Ring Test Resonance Phenomenon, using the specific drug as a reference control substance.

Similarly, the recorded trace of the electroencephalogram (EEG) was examined. When microscope slides of different parts of the brain are tested on the recorded EEG trace, they all produce various degrees of resonance, while tissue other than the brain do not produce any significant resonance. When the EEG of a patient with confirmed Herpes Simplex Type I Virus infection of the brain was examined, only the monoclonal antibody of the Herpes Simplex Type I Virus produced resonance with the recorded EEG trace of the infected area of the brain. Also, when the abnormal EEG trace is tested with the Bi-Digital O-Ring Test, the O-Ring will markedly open, depending on the degree of the abnormality. When the EEG trace of a patient with a viral infection of the brain, such as Herpes Simplex Type I Virus, is tested with an effective antiviral agent, such as Acyclovia or a more effective substance such as a mixture of EPA (Eicosa Pentaenoic Acid) and DHA (Docosa Hexanoic Acid), the abnormal ORing weakening phenomenon disappears completely.

Similarly, on the electromyogram (EMG) the muscle tissue identical to the muscle in which the EMG recording electrode was inserted produces maximum resonance, as compared with muscles from different parts of the body. In addition, when a muscle is infected by bacteria or a virus, a microscope slide of the bacteria or the monoclonal antibody of the virus produce significant resonance, depending on the degree of infection.

According to these findings, from any abnormal bioelectric recording such as ECG, EEG, or EMG as well as bioelectric potentials from other parts of the body, one can identify where the electrical signal is originating from and what bacteria, virus, or toxic substance may exist in the area where the potential is generated, using the Bi-Digital O-Ring Test Resonance Phenomena with various control substances. Furthermore, by testing various medications on the recorded trace of abnormal bioelectric potentials, one may find potentially effective medication.