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Abstract

In 1984, the author first developed a simple, quick, non-invasive, economical method of detecting cancer in specific internal organs, using the Bi-Digital O-RingTest (BDORT), with a microscope slide of specific cancer of a specific internal organ as a reference control substance. The detection rate for cancer screening was much greater than with any standard diagnostic tests. When imaging was performed using the BDORT, the area of positive response to the cancer positive slide was often much greater than the actual size of the cancer itself. This was due to the fact that most of the cancer tissue of the lungs or digestive system contained viruses such as HTLV-3 (often found in adenocarcinoma of the lung, stomach, head of pancreas, and colon) or HTLV-1 (often found in small-cell carcinoma of the lung and certain types of leukemia). The extent of the virus positive area was often far greater than that of the cancer tissue itself and was distributed in a much greater area surrounding the cancer. For this reason, the virus alone showed a response which could be mistaken for cancer tissue. The author succeeded in differentiating the exact location of cancer tissue itself from surrounding cancer related virus (with or without other microbes) positive area by using a pair of identical microscope slides with the same cancer tissue. One of the slides was exposed to ultra-violet rays (peak wavelength of 253.7 nm mercury vapor atomic resonance spectral line) for 40 seconds-4 minutes. After this exposure, the BDORT response to the virus (with or without other microbes) associated with the cancer tissue was completely eliminated, while the response to the cancer tissue was maintained. Using an ultraviolet exposed cancer slide, the imaging of the part of the body which responded to this virus-free cancer slide indicated die actual location of the cancer tissue, which was often confirmed by standard X-ray or other imaging methods when the thickness of the tumor was relatively large. These cancers detectable by standard laboratory tests had strikingly weakening response to the BDORT (-3.5 and -4), with ultra-violet exposed cancer slide as well as for antibody of Oncogen C-fos. The smallest size of cancer tissue detected by this method was less than 1mm in diameter in the very early stage of the cancer, which usually cannot be detected by current laboratory tests. The microscope slide of the cancer tissue with surrounding cancer associated viruses showed the extent of the virus infected area to which the cancer might spread in the future. The BDORT often showed that even effective medication did not sufficiently reach the cancer and surrounding cancer-related virus infected area due to a localized micro-circulatory disturbance, detected by an increase in Thromboxane B2; drug uptake was significantly increased by induced vasodilation, generally in the following order of effectiveness: positive Qi Gong, acupuncture, transcutaneous electrical stimulation, GE, calcium channel blocker, or beta-blocker. This simple, non-invasive, early diagnostic method of cancer tissue detection using an ultra-violet exposed microscopic slide or antibody of Oncogen C-fos or other cancer markers can be a very quick economical means of mass screening of the early stage of various cancers of the lung, breast, stomach, colon, head of pancreas, etc.

Keywords

Early detection of cancer Cancer associated viruses HTLV-3,HTLV-1 Adenocarcinoma (of the lung,colon,stomach,head of the pancreas)Small cell carcinoma of the lung Breast cancer Ultraviolet radiation Destruction of viruses and other microbes Bi-Digital O-Ring Test Antibody of Oncogen C-fos Anti-viral agents Anti-cancer agents EPA (Eicosa Penta-enoic Acid)Thromboxane B2 Microcirculatory disturbance Vasodilators Qi Gong Microscopic intracellular Bi-Digital O-Ring Test

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References

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