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Title: THE BIOPHOTON PHOSPHORESCENCE EFFECT OF HOMEOPATHICS ON CELL CULTURE

Chief Editor:
Judith Nagy, M.D.; Independent Medical Editor; Budapest, Hungary

Edited and Validated By:


Istvan Bandics, M.D.; Budapest, Hungary Gylila Panszki, M.D.; Budapest, Hungary Illya Brenner, M.D.; Institute of Oncology, Kiev, Ukraine Peter Smith, LCH; Cornwall, England Dima Sakharov, Ph.D.; Kiev, Ukraine Tony Hughes, D.A.c.; Dublin, Ireland Peter Bartlett, D.O.; London, England

Consultant:
Dr. Simon Gutl, M.D.; Hanover, Germany

Developed By:
The staff of Maitreya; Limerick, Ireland

This article was presented at the Pharma Expo in Budapest, Hungary; an international pharmacy exposition presented on November 10 - 13, 1994.

THE BIOPHOTON PHOSPHORESCENCE EFFECT OF HOMEOPATHICS ON CELL CULTURE

Abstract: Placed in a light-proof box is placed a Thorn EMI photon counter tube which counts visible light photons. (Secondary experiments were also done with infrared photons.) It is the hypothesis of this study that there is a photon dependence in biology, and also that the utilization of the immune system is modulated through various photons. Various cell cultures were placed into the light-proof box and studied for photon release versus controls. Then homeopathics were applied to the cell culture, and the photon release was then restudied. It was shown that different types of homeopathics had dramatic effects on the phosphorescence factors, or photon retention. As well, they affected the decay rate, and in certain cases, biophotons were produced which could not be explained in the normal system. The study further discusses the factors of biophoton release in the context of QED (quantum electrodynamics) as an explanation of the immune system.

Key Words:

Biophoton, radiation, increase, Fungi-Fugue homeopathic, Viral-Fugue homeopathic, Immunopoie homeopathic, influenza, bacteria, Bacteria Formula #2. Introduction: In the Quantum Biology books Dr. Nelson makes the point of a connection between quantum electrodynamics as one of the highest forms of theoretical physics and biology. Biology is usually fifty years behind physics in its ability to explain things, in that biology often spawns medicine techniques which are based on antiquated ideas but then become resistant to change. Theoretical physicists have recently taken on the understanding of more quantum terms, and quantum electrodynamics has recently received great applause as an explainer of many different physics events By now taking this quantum electrodynamic principle a couple of steps further, as is done in the Quantum Biology books, we see that there is definitely a place for the quantum electrodynamics as an explainer in biology. Quantum electrodynamics basically shows that the interdependence of any chemical, electron or other molecular event is photon dependent. Thus we must bring the photon into our analogy of biology. This simple experiment allows us to measure the basic photon release of different items in a light-proof box. Then we will study cells and cell cultures, and also how different homeopathics might change the photon release of these items. Method: A light-tight box lined with black velvet is designed to stop any external photons. A photon counter tube from Thorn EMI is then inserted into the box. Approximately five inches away from the two, we can insert a petri dish or other item, and then study the photon release, and actually count the photons released from the item in the box [Studies: 2, 3]. Dr. Kenyon and his team also have duplicated a similar type of event by using photon counters to determine the intensity of bioluminescence from humans [Studies: 4]. First an empty petri dish was studied. Here there was release of various photons, starting with a report of a high of 581 and a low of 439. There were sixty measurements done, one every two seconds, showing the time frame over a matter of two minutes. Once the item was placed into the box, the lid was closed. Two seconds after closing the lid, the photon counter tube was activated. It made its measurements over the following two minutes. Our first score shows the results of an empty box. The empty box would have a background of 300-400 different photons. These were usually from the phosphorescence of the materials within which provided a background. Also there was some backlash from the tube itself. So this is our background type of electromagnetic radiation, which allows us to make comparisons. Next, an empty agar plate was put in. Here a surge of photons is seen to start at

1,639; roughly decaying over the following two minutes to 500. This accounts for the phosphorescent effect of how different items store photons from room light. Once they are deprived of those photons, the photons can be released through phosphorescence. Thus agar was studied and utilized because of its ability to maintain different types of culture. Next we put a sample of foot fungus onto the agar plate and closed the box. We see that foot fungus has a dramatic number of photons, in that it started off at 3,504 and decayed to roughly to 500 within two minutes. Then, if we put four drops of our homeopathic known as Fungi-Fugue into the foot fungus on the agar plate and close the door, we can see now that the radiation surges to 4,240; an almost twenty-five percent increase in the amount of photon release, and some subsequent decay. This leads us to the possible conclusion that the homeopathic might induce an extra amount of biophotons from the fungus. Next a smear of mouth bacteria taken from a cold virus case was applied to another agar plate. Here we can see a release of different photons from the phosphorescence effect of the mouth bacteria; a release much greater than the agar plate empty. On our chart #6 we see that with the same mouth bacteria smear, if we add three drops of Viral-Fugue homeopathic, there is a dramatic surge in the number of photons radiating from the mouth bacteria. It should also be known that if we put only the Viral-Fugue onto the agar plate, there is a less than one percent increase in the actual photon release. In chart #7 we see that by using an increased amount of the Viral-Fugue, there is an increased amount of photons. In fact, here the baseline photons become so great as to display a type of bioluminescence. In charts #8 - #10, we observe what happens when a cold virus swash taken from oral mucosa is applied to the empty agar plate. When we apply three drops of an influenza type homeopathic, by increasing the amount of the influenza we also dramatically increase the photon release (charts #9 and #10). On charts #11 - #13, we see that when we take a sample of fingernail bacteria taken from a patient who had a bacterial infection of the fingernail and put it in with the homeopathic Immunopoie, there is a dramatic increase in the amount of photon release. Results: On pages 17, 19 and 19 in the Appendix, we see the result of a homeopathic that has failed in stimulating the biophoton. Here an engineered bacterial homeopathic was applied, known as Bacteria Formula #2. This formula was applied to the cell cultures, and actually decreased the number of photons. It was later found clinically that this formula had no effect on helping the body to deal with bacterial infections, and thus was omitted from the quality control aspects; it was found to be ineffective. As we can see, there is an ability of certain homeopathics to stimulate biophoton release. There is also the ability of certain homeopathics to impinge. This allows us to develop an engineering process along the lines of the QED phenomena that helps us to recognize the photon connection with various biological events. Our biophoton connection, thus, may be brought into an engineering process to help us to develop the best in quality homeopathics.

Discussion: As we look into the development of a biophoton analysis, we will need to utilize these types of techniques, not only in engineering but also in the scientific research, to establish the biophoton and homeopathy as needed measures in medicine.

THE BIOPHOTON PHOSPHORESCENCE EFFECT OF HOMEOPATHICS ON CELL CULTURE

BIBLIOGRAPH Y

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Medical Botany. Lewis. Wiley, 1977. Merck Manual (15th ed.). Edited by Berkow, M.D. Merck, Sharp and Dome Research Laboratories, 1987. Pathophysiology: The Biological Principle of Disease. Smith and Thier. Saunders, 1981. American Medical Association Home Medical Advisor. Edited by Clayman, Kunz and Meyer. Random House, 1988. Differential Diagnosis. Harvey and Bordley. Saunders, 1976. Statistics Manual. Research Dept. US Naval Ordinance Test Station. Dover, N.Y., 1960. The Essentials of Clinical Biochemistry. D. N. Barron. Elsevier Biomedical, Amsterdam, 1982. Gray's Anatomy. Henry Gray, Royal College of Surgeons. Running Press, Philadelphia. 1974. Homeopathic Pharmacopeia of the United States. Homeopathic Pharmacopeia Convention of the United States, Washington, D.C. June 1993. Physician's Desk Reference. Medical Economic Data, Inc. Montvale, N.J. 1992.

ARTICLES AND STUDIES 1. 2. 3. 4. A Practical Definition of Homeopathy. Maitreya; Limerick, Ireland; 1993. Phosphorescence and Chemiluminescence of Various Homeopathic Compounds. Maitreya; Limerick, Ireland; 1994. Towards a Theory of Living State (Part 1). Mishra; Applied Mathematics and Computation. Elsevier Science Publication, 1993. Measurement of Human Bioluminescence. Edwards, Kenyon, Taylor. The International Journal of Acupuncture and Electro Therapeutics, Vol. 15, pp. 84-94. 1990.

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